Library

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 85-114 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements of the small-angle scattering power and the degree of crystallinity in melt-crystallized high-density polyethylene have been used to evaluate the “amorphous” density in situ by the relation, \documentclass{article}\pagestyle{empty}\begin{document}$ (2\pi/V)\int_0^\infty {S\tilde g} (S)dS = (\rho_{\rm c} - \rho_{\rm a})^2 \upsilon_{{\rm er}} (1 - \upsilon_{{\rm er}}) $\end{document} where V is the irradiated volume and ḡ(S) is the “slit-smeared” absolute intensity. The amorphous density is a function of sample history and is always higher than the extrapolated melt density. After slit-height correction, and within the experimental error, the ratio of the two observed long periods is 2:1 at all temperatures (25--126°C). The lamellar thickness and the average interlamellar spacing are obtained from the degree of crystallinity and the first corrected long period. At increasing temperatures between 25°C and 110°C, the lamellae become thinner while the interlamellar zone expands by almost half. Over this range the changes are reversible with temperature. Above 110°C, both the lamellae and the interlamellar region expand with temperature. The thickening is partially reversible upon recooling. Other results obtained include measurements of stacking disorder and of microstructural changes with crystallization temperature and with time at ambient temperature.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 143-160 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Work on two sheet organosilicon polymers, one derived from the mineral chrysotile and the other from the mineral apophyllite, is described. This work provides direct evidence that both these polymers are composed of sheets. In addition, it shows that in the chrysotile-derived polymer the sheets curl into scrolls, and that in the apophyllite-derived polymer the sheets are essentially flat.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 209-243 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The shear creep and creep recovery behavior of narrow molecular weight distribution polystyrene samples of low molecular weight, 1.1 × 103, 3.4 × 103, and 1.57 × 104 are reported as a function of temperature, near and above the glass temperature. Time-temperature equivalence for the total creep compliance is found to be nonapplicable, and in fact the steady-state recoverable compliance, Je, is a strong function of temperature. The time-scale shift factors for the recoverable compliance are analyzed in the light of free volume theory. Viscosity data are presented for samples with molecular weights between 1.1 × 103 and 6.0 × 105. The temperature dependence of the characteristic time constant ηJe can be explained in terms of free volume concepts whereas that of viscosity η cannot. Effects of residual molecular weight heterogeneity are demonstrated.
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 295-311 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A theoretical calculation of the Hv light-scattering patterns for deformed three-dimensional spherulites is presented. Affine deformation is assumed. The optic axis of the scattering element is allowed to lie at an arbitrary angle ß to the radius which is permitted to change in the course of the deformation in a manner that may depend upon the angular location in the spherulite. The consequences of twisting of the optic axis about the spherulite radius are also explored.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 331-343 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The adsorption of polydimethylsiloxane polymers from solution on glass has been studied. The amount of polymer adsorbed depends markedly on the solvent because of specific solvent - surface interactions. The presence of silanol groups in the polymer, particularly as endgroups, markedly increases the amount of polymer adsorbed. Large differences are shown between the adsorption of the commercially available, and fully trimethylsilylated polydimethylsiloxanes of narrow molecular weight distribut on. Possible adsorption mechanisms are discussed.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 383-384 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 421-430 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A method is given for the analysis of long-chain branching in polymers by using combined GPC and intrinsic viscosity measurements. A computer program was written to evaluate branching indices by a tabular, iterative method. The method was applied to the evaluation of long-chain branching in low-density polyethylene.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 431-435 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effects of stereoregularity on the low-temperature relaxation processes were studied by dynamic mechanical measurements on isotactic and syndiotactic polyisobutyl methacrylates (iso-PiBMA and syn-PiBMA). The α, β, and γ relaxation processes were observed in both stereoregular forms. Both the α, and β loss peaks were at lower temperatures for iso-PiBMA than for syn-PiBMA. The γ loss peak was observed at about -155°C at 30 Hz for both forms, and the apparent activation energy of this process was same for both samples within experimental error (6.7 ± 0.5 kcal/mole). It was reduced from these results that the α and β processes are both considerably influenced by the isotactic configuration but the γ process is not.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 15-26 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The gelation reaction of acetoguanamine with formaldehyde was investigated in the light of the gelation theory for tetrafunctional amino resins described in the previous paper. The gel time and extents of reaction of formaldehyde, amino groups, and imino groups varied with the molar ratio in the feed, but values of K (the ratio of the rate constant for condensation to that for addition) and k (the ratio of the rate constant for addition of the imino group to that of the amino group) were nearly constant. When the catalyst concentration was increased, the gel time, extents of reaction of each functional group, and the values of K and k varied; in particular K increased markedly. From the results of varying the molar ratio and concentration of acidic catalyst, it was found that the number of methylol groups per molecule of acetoguanamine at the gel point was influenced by the reaction conditions but the number of methylene linkages per molecular of acetoguanamine was nearly constant at about 0.6, regardless of reaction conditions. The number-average molecular weights up to the gel point varied with the reaction conditions, but at the gel point they were all nearly constant at about 385.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 543-555 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Photocurrents developed in polyethylene in the wavelength range 360-180 nm have been measured. The action spectra show features which can be related to the corresponding features in the absorption spectrum, and in addition there is electron injection from the metal electrode at a wavelength determined by the electrode material. The time dependence of the response indicates that a long-lived space charge is formed in the material.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 11
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 569-576 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Large photocurrents have been observed in films of some simple polymers (containing no π-orbitals), of which poly(vinyl fluoride) is a typical example. Not only are the currents large (up to 10-5 A/cm2) but also they are capable of being excited by light in the visible wavelength region where absorption by the polymer is too low to be detectable. The results indicate that the effects are electronic, rather than ionic, in nature.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 12
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 577-584 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It was previously shown that for a stationary random copolymer of A, B, and C, we have in general p(AB) + p(AC) = p(BA) + p(CA), etc., in place of p(AB) = p(BA) which is valid for a stationary binary copolymer. Here, p(AB) for example, is the probability that a randomly picked pair of consecutive comonomers in the polymer consists of an A followed by a B. For a stationary ternary copolymer produced by a first-order Markovian addition mechanism, we show that PABPBCPCA/PACPCBPBA = k, where k is a constant characteristic of a particular set of three monomers but independent of its composition. Here, PAB is the conditional probability of finding a monomer of B given that its immediate predecessor is an A. We further show that if the individual rate constants of the monomer additions involved take a special form such as used in the Alfrey-Price Q-e scheme, then we have k = 1 irrespective of the kinds of monomers, and in addition we have p(AB) = p(BA), p(AC) = p(CA), etc. Thus, although these latter results were previously proposed by Ham as an alternative basis to supplant the Q-e scheme, they may rather be regarded as mathematical consequences of special assumptions adopted for the form of the individual rate constants. For a stationary random copolymer of four components A, B, C, and D, we have p(AB) + p(AC) + p(AD) = p(BA) + p(CA) + p(DA), etc., in general. For a first-order Markovian four-component copolymer, we show that there are seven different combinations of the conditional probabilities that are constants (k1, k2,…, k1) independent of the monomer composition. Again, if we assume the same special form for the rate constants involved, we find that all the seven constants k1, k2, …, k7 reduce to unity and p(XY) = p(YX) for X,Y, = A, B, C, D.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 13
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 717-729 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Several copolymers as well as homopolymers of vinylidene chloride and vinyl chloride have been examined by Raman spectroscopy. Probabilities of concentrations of monomer sequences have been calculated from known reactivity ratios. Surface scattering intensities at some frequencies were found to be linearly proportional to specific microstructure concentrations. Normalization of scattering intensities was accomplished using the intensity of the CH2 asymmetric stretching mode at 2926 cm-1, which is common to all samples examined. Good correlation was found for the concentrations of comonomer sequences {B}, {BB}, {BBB}, {AA} and {AAAA} in which A denotes vinylidene chloride and B vinyl chloride.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 14
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 755-758 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The mass flux entering the Fick's diffusion equation is considered as an arbitrary analytical function of concentration, concentration gradient, and of the gradient of concentration gradient. The restrictions imposed on the flux by the principle of material objectivity are stated and briefly discussed.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 15
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 759-762 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 16
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1287-1303 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The viscoelasticity and volume expansion of the raw polymerizate of ethylene-propylene copolymer with vinyl chloride grafts, and of the individual components has been studied. The raw polymerizate (composite) and the pure ethylene-propylene-vinyl chloride graft copolymer were found to consist of two phases. The pure graft copolymer has an ethylene-propylene matrix containing some fraction of poly(vinyl chloride) (PVC) grafts and a microphase with the remainder of the PVC grafts. The raw polymerizate consists of a PVC matrix plasticized with ethylene-propylene chains and a microphase of the ethylene-propylene copolymer. An attempt has been made to calculate the participation of components in microphases and the minimum dimension of the PVC microphase aggregates.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 17
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1333-1339 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The lattice-theory equations for the surface tension of polymer solutions based on the parallel-layer model have been extended to include more than two components. The surface tensions of tetrachloroethylene solutions of some blended polydimethylsiloxane fluids have been measured at room temperature. The results are in nearly quantitative agreement with the theoretical calculations.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 18
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1371-1378 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new relaxation process, explaining the change of elasticity in rubberlike polymers at critical stress (0.1-0.5 kgf/cm2) has been discovered. This process is characterized by the low value of activation energy (weak temperature dependence of relaxation times) and large sizes of kinetic units (strong dependence of relaxation time on stress). Critical stress depend on temperature and for rubberlike polymers turns to zero at 40°-60°C. Mechanism of the phenomena can be explained by the existence of the ordered molecular microregions, creating additional crosslinking points of nonchemical nature with free chains of the network, breaking up at critical stress. Observed phenomena is analogous to the process of forced rubber elasticity of those polymers in glassy state. Critical stress is analogous to the limit of forced rubber elasticity below glass transition temperature.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 19
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1449-1469 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Wide-line NMR spectra have been obtained on an oriented sample of drawn nylon 66 fibers at temperatures between -196°C and 200°C and at alignment angles between the fiber axis and the magnetic field of 0°, 45°, and 90°. At -196°C, 20°C, and 180°C, the complete angle dependence of the NMR spectrum has been measured. The second moments of these spectra have been compared to theoretical second moments calculated for various models of chain segmental motion in an attempt to elucidate the mechanisms involved in the low-temperature segmental motion (γ process) and the high-temperature segmental motion (αc process). In agreement with earlier suggestions, the present results indicate that the γ process consists of segmental motion in noncrystalline regions. The overall decrease in second moment caused by the γ process is consistent with a model in which all noncrystalline segments rotate around axes nearly fixed in space. Furthermore, this decrease shows a pronounced dependence on the alignment angle. It is believed that this is due to tie molecules which become highly oriented along the fiber axis during drawing; their axes of rotation will therefore be nearly parallel to the fiber axis. The segments in noncrystalline entities such as chain folds and chain ends are less well oriented along the fiber axis and make an essentially isotropic contribution to the second moment decrease. The second moment at 180°C indicates the presence of considerable motion in the crystalline regions, and this motion is denoted the αc process. The second moment Sc of the crystalline regions is strongly dependent on the alignment angle, the predominant feature being a relatively high value of the second moment when the fiber axis is directed parallel to the magnetic field. This is in qualitative, but not quantitative, agreement with the motional model recently advanced by McMahon, which assumes full rotation of the chains around their axes. Excellent quantitative agreement with experiment has been obtained by superimposition of rotational oscillation around the chain axis of amplitude roughtly 50°, and torsion of the chains with neighboring CH2 groups oscillating around the C—C bond with a relative amplitude of about 40°. A model in which the chains perform rotational jumps of 60° between two equilibrium sites has also been considered (60° flip-flop motion). A distinction between this model and rotational oscillation has not been possible.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 20
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1525-1529 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 21
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1553-1577 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: As is well known, the chemical potentials of polymer and solvent in solution and, hence, the Flory-Huggins interaction parameter χ can be determined from scattered light intensities from dilute and concentrated solutions of the polymer in the solvent concerned. Preferably, measurements should be performed at temperatures as low as possible, provided the temperature exceeds the cloudpoint for the concentration used. It is shown that the lower the temperature and, consequently the higher the scattered light intensity, the better is the accuracy of the parameters obtained. At each temperature the scattered light intensity shows a maximum at some concentration. Below the theta temperature the ratio of scattered light intensity and concentrations also shows a maximum at some concentration. The values and the concentrations of these maxima for various temperatures enable the maximum of the spinodal to be determined. The spinodal itself can be determined by an extrapolation procedure of the reciprocal scattered light intensities. Measurements have been performed with three narrow-distribution polystyrene samples in cyclohexane. On the basis of the results, χ, and its dependence on concentration, temperature, and molecular weight can be determined to high accuracy.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 22
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1641-1655 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The morphology of high-density polyethylene crystallized under simultaneous pressure and shear in an Instron capillary viscometer has been examined by scanning electron microscopy, electron microscopy, and selected-area electron diffraction. Two distinct fibrous morphologies were observed in these unusually transparent strands. The outer sheath was composed of fibers, 3000 Å in diameter, aligned parallel to the extrusion direction and apparently interconnected by a lamellar cross texture. A highly crystalline ribbon texture composed of fine fibers, 200-250 Å in diameter, dominated the inner core. Sharp-spot electron diffraction patterns obtained from these central ribbons indicated a high degree of c-axis orientation parallel to the fibers and an extended-chain crystal structure. The melting behavior of both irradiated and unirradiated strands examined by differential scanning calorimetry was consistent with the formation of two distinct crystalline morphological units.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 23
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1681-1691 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The influence of the nature of exchangeable cations on the tacticity of poly(methyl methacrylate) (PMMA) prepared from montmorillonite-MMA adsorption complexes was investigated. The strength of ion-dipole interactions was estimated either by the value of the electrostatic interaction potential or by the value of the carbonyl-stretching frequency shift. It was shown that Pi, the percentage of isotactic triads in the polymer, increases with increasing strength of the ion-dipole interactions, while the persistence ratio and the mean length of closed isotactic (or syndiotactic) sequences remain essentially unchanged regardless of the nature of the cation. It was shown that values of Pi may vary from 0.15 for weakly interacting ions to 0.5 for strongly interacting ones, reaching at the upper limit the value calculated from the model proposed in a previous paper, thus confirming its validity.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 24
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1693-1702 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Differential thermal analysis (DTA) of some commercial nylons has disclosed some anomalous phenomena with respect to the glass transition, generally considered to occur at 40-50°C. On the first heat cycle the transition occurs normally. On cooling, however, no corresponding transition occurs, and on an immediate rerun the transition has disappeared. If another DTA thermogram is made after a few hours, the transition begins to reappear, but at a temperature lower by a few degrees. After about five days rest, the transition is again normal in size and temperature. On annealing at 75°C, the 43°C transition is pushed up to about 92°C. On resting after annealing, transitions appear at both 40 and 92°C. These phenomena are explained in terms of the slow formation of a hydrogen-bonded network in the amorphous regions of the polymer. It is the disruption of this network that is normally considered to be the glass transition in nylons. The network is slow in re-forming because of problems involved in matching up potential hydrogen-bonding sites, which are, of course, distributed at intervals along the polymer chain. The temperature at which the network is disrupted is apparently dependent not so much on the ratio of bonding to nonbonding sites, as on the temperature at which it was formed.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 25
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1793-1805 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Detailed critical examinations of three aspects of nitric acid treatment of polyethylene are reported. (1) The endgroups introduced by the nitric acid are examined. It is concluded that in samples degraded to a single-crystal traverse stage, carboxyl features only as endgroup, and conversely each chain-end is terminated by such a group. Consequently, the carboxyl content can be used for quantitative characterization of the cut chain length. The function and position of the nitro group remains unexplained. (2) The morphological selectivity of the nitric acid-induced degradation is scrutinized. It is concluded that the crystal core is attacked and thinned by the acid; the slowing down of the reaction is principally due to accumulation of reaction products. Accordingly, the usual distinction between a vulnerable amorphous layer and a resistant crystal core is not justified on the basis of such degradation experiments. It follows that meaningful structural information is obtained only when the relevant crystal properties are studied as a function of chain cutting, assessed from the molecular weight distribution (GPC), as opposed to that of degradation time alone. (3) The role of sample consistency and reagent strength has been examined. It is demonstrated that for the reaction to be sufficiently uniform throughout the sample for the results to be meaningful, the reaction rate has to be slow compared to the rate at which the reagent diffuses into the specimen. To realize these conditions, finely dispersed samples and weak reagents were found to be favorable
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 26
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1871-1885 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Several samples of a copolymer were examined by means of equilibrium centrifugation in a density gradient. The results for the samples without compositional distribution (homogeneous polymers) were used to determine the relation between the chemical composition and the distance from the center of rotation. For one of the homogeneous polymers a quantitative analysis of the schlieren curve was made in order to show the kind of accuracy that can be achieved. For the inhomogeneous polymer it was found that the schlieren curve could, in principle, be described quantitatively by the assumption that fluctuations in composition are independent of fluctuations in molecular weight, but on this basis the average square of the fluctuations in composition is more than four times smaller than the value derived from chromatographic data. A more satisfactory explanation of the experimental results is provided by assuming a linear correlation between average molecular weight and composition, but it is not claimed that this is necessarily the only model that explains the data.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 27
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1887-1905 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Time-dependent, apparent heat capacities of glucose, poly(vinyl chloride), polystyrene, selenium, poly(methyl methacrylate), and poly(2,6-dimethyl-1,4-phenylene ether) in the glass transition region were determined by differential thermal analysis. The thermal history was set by linear cooling at rates between 0.007 and 160°C/min. Linear heating for analysis was carried out at rates between 0.3 and 600°C/min. Average activation energies of 52, 81, 90, 54, 77, and 108 kcal/mole, respectively, were evaluated by using the hole theory of glasses previously developed. Within experimental limitations all data could be described quantitatively by the theoretical expressions using only one parameter, the number of frozen-in holes, to described the thermal history. Experimental and theoretical limitations are discussed.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 28
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1915-1918 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 29
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A mathematical development interrelating the orientation distribution functions of three kinds of orientation units for a polymer spherulite (i.e., a crystal lamella, a crystallite, and a given reciprocal lattice vector of the crystallite) is formulated on the basis of series expansions of the distribution functions in generalized spherical harmonies. Two types of uniaxial deformation models of a polyethylene spherulite, taking account of micronecking and untwisting of crystal lamellae, and of chain tilting and untwisting of crystal lamellae, respectively, both in addition to affine deformation of the lamellae are discussed. The models are tested by comparison of the theoretical orientation distribution functions of some reciprocal lattice vectors of the crystallite with the results of x-ray diffraction experiments.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 30
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2033-2042 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Wide-line NMR spectra of nylon 66 fibers have been obtained at different alignment angles between the fiber axis and the magnetic field, at varying water contents (H2O and D2O), and at different temperatures. At 28°C the spectrum of the dry fibers consists of a nearly structureless broad line. At water regains of 1.4% by weight (dry basis) and higher a sharp line appears which originates from highly mobile water molecules. The width of this line decreases with increasing water content, implying an increase of water mobility. Moreover, the width is a function of the alignment angle; this shows that the water is not reorienting isotropically owing to specific water-polymer interaction. The amount of mobile water is always smaller than the amount of water absorbed. At water contents close to saturation, a mobile polymer line appears with a width intermediate between the broad line (immobile polymer) and the sharp water line. This line, most clearly observed at an alignment angle of 0°, is due to a shift of the αa process to lower temperatures in the presence of water. A similar line is observed in the dry fibers at 120°C. It is shown that the αa process decreases the NMR second moment only slightly. The shift of the high temperature drop in second moment to lower temperatures in the presence of water is therefore interpreted as due to a shift of the αc process, and not of the αa process, to lower temperatures.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 31
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2099-2103 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 32
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2119-2130 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A general theory of non-Gaussian elasticity is presented for real polymeric chains having fixed bond angles and restricted internal rotations. The theory contains the displacement-vector distribution given by Nagai, and the Flory-Wall-Hermans procedure is used for the calculation of network properties. Whereas the treatment is valid for all types of polymer chains, it is not totally satisfactory from a practical standpoint because of a slow series convergence if the chains are stiff. It is best utilized for flexible polymers under conditions of light crosslinking. Detailed network behavior is investigated only for polyethylene type chains having uncorrelated internal rotations. In this instance the fractional contribution fe/f of the internal energy of the total force f is found to be a function of elongation at high degress of stretching. It may decrease, or increase, depending upon the sign of fe/f at low elongations. Furthermore, the variation of fe/f with elongation is independent of the fixed bond angle of the chain backbone. Stress-strain behavior and energy-strain behavior are in opposition, i.e., when the non-Gaussian contribution to the stress is greatest, it is the least for the ratio fe/f, and vice versa. The presence of correlated internal rotations would not be expected to greatly alter these general conclusions.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 33
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2247-2251 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 34
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Two linear polyethylene fractions (Mη, 11,260 and 100,000) and mixtures of these fractions have been isothermally crystallized from the melt under pressures up to 3000 atm. Characterization of individually crystallized fractions with transmission electron microscopy indicates that pressure can be used to produce a crystallite whose thickness is a measure of the chain length within it. Although the high molecular weight fraction yields spherulites containing individually varying lamellae thicknesses, the maximum thickness of each lamella is a measure of the chain length within it. Both electron micrographs and differential thermal analysis results show that crystallization of homogeneous mixtures of the high and low molecular weight fractions under high pressure results in a distinct fractionation and segregation according to molecular weight.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 35
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A method is described and a computer program outlined whereby gel-permeation chromatographic analysis of fractions from gradient-elution fractionation of branched polyethylenes provides a complete molecular weight evaluation of each fraction and the parent resin. The procedure involves the use of the universal calibration concept of Benoit et al. in a way that eliminates the ambiguities present in attempts to apply it directly to whole polymers. The resultant molecular weight data for fractions, when related to their solution viscosity and low-shear melt viscosity and to their infrared analysis, provides a total structural evaluation of a branched polyethylene resin, including molecular weight molecular weight distribution and the distribution of both long-and short-chain branching. The potential of this method for providing a comprehensive structural evaluation of branched polyethylene is illustrated by examples of its application in the analysis of some commercial resins.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 36
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2255-2258 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 37
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 27-42 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A three-dimensional polarized infrared technique was used to obtain information about molecular orientation in both uniaxially and biaxially drawn nylon 6 films. The 835 and 930 cm-1 bands were used to describe the orientation of the A (extended chain) conformation while absorptions at 1175 cm-1, and 1120 cm-1 and 1075 cm-1 were used to give some information about orientation of the B (twisted chain) conformation. On the basis of the 835 and 930 cm-1 bands, it was shown that the hydrogen-bonded sheets made up of chains in the A conformation are parallel to the film surface in the biaxially drawn film. Uniaxially drawn films obtained by drawing both at 100 and 150°C showed a high degree of chain alignment in the draw direction for the A conformation at draw ratios greater than 2.5. Some planar orientation was also observed in these uniaxially drawn films for both the A and B conformations at high draw ratios.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 38
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 59-66 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Crystals of poly-trans-1,4-butadiene of uniform size have been grown from three solvents (n-heptane, methyl isobutyl ketone, and toluene) by using a minimum dissolution temeprature technique. The percentage of double bonds available for reaction in the crystals was determined by epoxidation in suspension; crystal thicknesses were measured by electron microscopy. These values were used to calculate the number of monomer units per fold. The number of available double bonds was found to increase with decreasing molecular weight, evidence for the presence of non-reentrant chains (cilia) at the crystal surfaces. The nature of the chain fold in poly-trans-1,4-butadiene crystals is discussed.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 39
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 161-173 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new device for measuring the electrostriction constant of polymer films is described. Observed values for various polymers except poly(vinylidene fluoride) and poly(methyl methacrylate) agree well with those calculated from the Clausius-Mosotti equation. Elongational piezoelectricity, the pyroelectric current, and the electrostriction constant are measured for undrawn and roll-drawn poly(vinylidene fluoride) films. The piezoelectricity and pyroelectric current are attributed to space charges antisymmetrically distributed along thickness direction of the film for two reasons: (1) the polarity coincides between these two phenomena for all specimens, and (2) the piezoelectricity and the electrostriction constant have the same anisotropy for drawn films. Similarity of signs between piezoelectricity and pyroelectric current is observed also in poly(vinyl chloride) films. The electrical behavior of poly(vinylidene fluoride) is interpreted in terms of the ferroelectric nature of the β-form crystal.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 40
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 181-186 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A γ-phase to α-phase transformation in a specimen of isotactic polypropylene crystallized under conditions of high pressure was induced by drawing at 100°C. X-ray studies showed that the unoriented component remained in the γ-phase, and that the oriented component was found only in the α-phase. This evidence supports a previous suggestion that the phase transformation is martensitic in character. The consequences of such an assumption are discussed. The role of dislocations in polymeric systems is generally believed to be not too significant, but since martensitic reactions involve cooperative movements of atoms, an exception in this case is suggested. A possible mechanism for the phase transformation is suggested.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 41
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1603-1627 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Transition and relaxation phenomena in 26 structurally related polyquinoxalines and other aromatic polymers were studied over a temperature range from 70 to 770°K by means of calorimetric, dilatometric, dynamic mechanical, and dielectric techniques. Differential thermal analysis and x-ray data showed these polymers to be essentially amorphous. The lack of crystallinity is attributed to geometric isomerism, resulting in conformational as well as configurational disorder. Calorimetric measurements gave discontinuities in heat capacities ranging from 12 to 54 cal/°C per mole of repeat-unit structures and provided unambiguous assignments of glass transition temperatures of these polymers. Depending upon structure, Tg varied from 489 to 668°K. Thermal expansion curves of annealed bulk polymer samples between 70 and 770°K exhibited only one discontinuity over the entire temperature range, namely at Tg, thus indicating the absence of any motion leading to transitions in the solid state of these polymers. Viscoelastic properties were obtained by means of torsional braid analysis and a longitudinal vibrational apparatus. In a typical case, the dynamic mechanical relaxation spectrum contained three loss maxima. A peak of low amplitude occurring at 483°K was attributed to impurity effects, resulting from endgroups and species of low molecular weight. The second and only major relaxation process occurred at 579°K, in the glass transition interval. A third, weak loss peak of unknown origin was found in the liquid state at 683°K. On the other hand, the dielectric loss curves of various polymers exhibited only one broad and strong absorption maximum at temperatures 30 to 100°K higher (depending upon a particular polymer) than equivalent major mechanical loss peaks. These differences are interpreted from a mechanistic point of view. Major mechanical relaxations occurring in the glass transition interval of these polymers are proposed to result from translational motions.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 42
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1669-1679 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The fluorescence quenching of the doubly charged quinine cation by Fe++, Ag+, and Br- was studied in the presence and absence of polyvinylsulfonate (PVS). The quenching by cationic species was greatly enhanced by PVS at low polyion concentrations; at higher concentrations of PVS, the fluorescence intensity increased owing to displacement of the quinine cations from the polyion domain. Quenching of quinine fluorescence by Br- was repressed by PVS. Interpretation of the data with the use of Fe++ as the quenching agent led to “effective concentrations” of counterions in the polyion domain similar to those calculated from the catalysis of the redox reaction of Co(NH3)5Cl++ with Fe++. This may indicate that the reagent ions are not rigidly bound to the polyion chain, since such binding would affect differently processes with high and low activation energies. The Stern-Volmer constant for self-quenching of the quinine fluorescence can also be obtained from fluorescence intensity data in PVS solution.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 43
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1703-1717 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The viscoelastic properties of a 4% solution of monodisperse polystyrene (molecular weight 394,000) in Aroclor 1260 were determined by the following techniques: creep recovery, stress relaxation upon cessation of steady flow, dynamic measurements, and normal stress difference and shear stress measurements in steady flow. All measurements were carried out with cone and plate geometry in a Weissenberg rheogoniometer. The modification of this instrument to perform creep and creep recovery experiments by use of an air-bearing suspension and an air-turbine drive is described. A broad range of shear rates and frequencies encompassing both linear and nonlinear behavior was employed. The elastic behavior is described in terms of the recoverable shear strain s or the steady-state compliance Je°. The first three techniques gave identical results for Je° in the range of linear viscoelasticity for which it is defined. The normal stress difference measurements confirmed Lodge's relation s = (P11 - P22)/2σ21. Reasons for previous experimental disagreement with this result are discussed.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 44
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1747-1761 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The contribution to the disorder scattering by imperfect spherulites resulting from fluctuations in the magnitude of the anisotropy is analyzed for two-dimensional spherulites. The fluctuations are described in terms of a parameter characterizing the meansquare amplitude of the fluctuation and a correlation function describing the distance over which the correlation occurs. Cases considered are those where the correlation depends on either the radial or the angular separation of the scattering volume elements. As with the case of disorder in orientation, one finds that disorder in anisotropy may result in a nonzero value of intensity at μ = 0° and 90°, a decrease in the higher-order variation of scattered intensity with θ, and an increase in the intensity of scattering at higher values of θ over that for a perfect spherulite. In addition, disorder in the angular direction leads to an increase in the scattered intensity at small values of θ as compared with the zero intensity of scattering from a perfect spherulite at θ = 0°.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 45
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1777-1791 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ozone has been used as a selective oxidizing agent for degrading polyethylene single crystals at room temperature in order to confirm and extend results on surface structure obtained by use of fuming nitric acid at temperatures above 60°C. The surfaces of the crystals were rendered highly accessible to the ozone gas by preparing the crystalline material in a highly expanded form; the solvent in which the crystals were suspended was removed by sublimation from the solid state. The extent and nature of the reaction were studied by measuring the increase in weight and in density, by direct chemical analyses, and by making use of infrared spectroscopy and gel-permeation chromatography. It was found that the surfaces of the crystals are attacked at room temperature by ozone, with resulting chain scission, and the broad features of the chemical reaction were established. Some folded chains are found to be as long as the original thickness of the crystal, and once folds have been cut, continuing reaction shortens the chains. In the early stages of the degradation, during which most of the weight increase takes place, the density of the crystals increases, and the magnitude of the increase is that expected from the increase in weight alone, i.e., assuming no increase in effective volume.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 46
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1907-1910 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 47
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1955-1976 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effects of mean residence time, initiation rate, and emulsifier concentration on particle formation, particle growth, and polymerization rate are examined for the emulsion polymerization of styrene in a completely mixed continuous stirred-tank reactor. Experimental measurements of number of particles, particle size distribution, polymerization rate, and molecular weights are compared with theoretical predictions. A theoretical model which incorporates Stockmayer's modification of the Smith-Ewart theory into the particle growth equation allows reasonably accurate prediction of polymerization rate, particle formation rate, and particle size distribution. Agreement between experimental measurements of number-average and weight-average molecular weights and a theory based on Smith-Ewart case 2 kinetics is also reasonable.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 48
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2009-2021 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The storage (G′) and loss (G″) shear moduli have been measured in the frequency range from 0.04 to 630 Hz for solutions of narrow distribution polystyrenes with molecular weights (M) 19,800 to 860,000, and a few of poly(vinyl acetate), M = 240,000. The concentration (c) range was 0.014-0.40 g/ml and the viscosities of the solvents (diethyl phthalate and chlorinated diphenyls) ranged from 0.12 to 70 poise. Data at different temperatures (0-40°C) were combined by the method of reduced variables. Two types of behavior departing from the usual frequency dependence describable by the Rouse-Zimm-Tschoegl theories were observed. First, for M ≅ 20,000, the ratio (G″ - ωηs)/G′ in the neighborhood of ωτ1 = 1 was abnormally large and the steady-state compliance Je0 was abnormally small, especially at the lowest concentrations studied. Here ω is circular frequency, ηs solvent viscosity, and τ1 terminal relaxation time. Related anomalies have been observed by others in undiluted polymers at still lower molecular weights. Second, at the highest concentrations and molecular weights, a “crossover” region of the logarithmic frequency scale appeared in which G″ - ωηs 〈 G′. The width of this region is a linear function of log c; the frequency dependence under these conditions can be represented by a sequence of Rouse relaxation times grafted on to a sequence of Zimm relaxation times. For each molecular weight, the terminal relaxation time τ1 was approximately a single function of c for different solvents of widely different ηs. At lower concentrations, τ1 was close to the Rouse prediction of 6ηM/π2cRT, where η is the steady-flow viscosity; but at higher concentrations, τ1 was proportional to η/c2 and corresponded, according to a recent theory of Graessley, to an average molecular weight of 20,000 between entanglement coupling points in the undiluted polymer.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 49
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2081-2093 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Terephthalamide nylons with two to five carbon atoms in the aliphatic portion of the chain have been crystallized from aqueous solutions of hexafluoro-2,2-propandiol. The 3T and 4T nylons in particular form rodlike crystals. Indications are that these are bundles of cylindrical structures about 50 nm in diameter. Electron diffraction shows the symmetry to be C2v. Films of the nylons were drawn with great difficulty. The x-ray diffraction on the films is consistent with a monoclinic structure, though the crystal structure could not be positively established. There is some evidence for a polymer chain alignment perpendicular to the long axis of the rods.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 50
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2043-2060 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In order to elucidate the relations between morphological habits and chemical structure of polymers, poly(ethylene sebacate), poly(hexamethylene sebacate) and poly(decamethylene 1,16-hexadecanedicarboxylate) were crystallized from dilute solutions in n-hexanol, isoamyl acetate etc., and were studied with the electron microscopy and x-ray diffraction. The crystal structure of these polyesters are tentatively determined. Morphological “regularity” and “simplicity” of the single crystals are correlated with the chemical structure of the polymers. The crystallization conditions under which “regular” and “simple” single crystals are obtained are relaxed with increase of methylene sequence length in chemical repeat unit. The Bragg extinction bands in the single crystals of poly(hexamethylene sebacate) and poly(decamethylene 1,16-hexadecanedicarboxylate) suggest nonplanar nature of these crystals. The molecular chains in the poly(ethylene sebacate) single crystals are inclined from the normal of the basal plane; the fold surface corresponds to the (001) plane.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 51
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2105-2108 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 52
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2131-2135 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It is shown that the glass transition temperatures of the ionic acrylates are subject to the same correlation as found for the phosphates, silicates, and ionenes; the equation is Tg = 730 (q/a) - 67, where q is the cation charge and a the separation between centers of charge for the cation and anion.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 53
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 609-614 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Difficulties have been encountered in experimentally measuring the stress-relaxation modulus for systems with steep slopes in the primary transition region. The usually applied “factor-of-ten” rule is shown to apply in these cases as well as in cases where the relaxation is slower; with the steep slope, however, the rule offers little help, since the decay in the modulus is so fast that stresses are usually very small at times when direct modulus calculations may be made. A technique is suggested which allows calculation of the modulus in this difficult region. A slow constant strain-rate deformation is followed by a constant strain period. Modulus values for times during the constant strain rate period are calculated using well known relationships. Long-time values are calculated from the definition of the modulus (the factor-of-ten rule being employed) and a recursion relation is developed which is used for modulus calculations during the constant strain period at relatively short times where effects of strain rate are important. Starting values for the recursion relation are long-time moduli which can be calculated directly.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 54
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 645-658 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Fourier transform method of Vonk and Kortleve for the analysis of small-angle x-ray diffraction (SAXRD) from semicrystalline polymers has been compared with a modified direct method, originally due to Tsvankin. SAXRD data for three melt-crystallized polyethylene samples have been analyzed in terms of the mean true periodicity, mean crystal length, and mean length of amorphous segments. The two methods of analysis yield substantially equivalent results for all three samples. Calibration curves for the Tsvankin analysis are tabulated, and the relative merits of the two methods of analysis are discussed. With either method, information about the diffracting structure may be deduced that is not available from a simple measurement of the position of the SAXRD maximum. In fact, direct application of the Bragg law to any but the sharpest maximum yields a spacing (the long period) that lacks direct physical significance.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 55
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1417-1447 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The stress-optical coefficient of poly-1,4-butadiene is measured as a function of strain, cis/trans ratio, and degree of swelling. Deviations from the Kuhn-Grün theory are found which are reduced upon swelling. Results are interpreted in terms of the Shindo-Stein theory of birefringence of polymers containing statistical segments of different sizes. This interpretation for the unswollen polymer leads to the unreasonable conclusion that the cis segment is considerably longer than the trans. Reinterpretation for the swollen polymer leads to the more reasonable conclusion that the trans segment is slightly longer than the cis. The dependence of the stress-optical coefficient on the nature of the swelling solvent is similar to the observations of Gent and Nagai and is believed to result from the effect of internal field from anisotropic solvent molecules. It is felt that the value of the stress-optical coefficient for the dry rubber is modified by the internal field from somewhat locally ordered neighboring polymer molecules.
    Additional Material: 22 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 56
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1579-1590 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The water permeability K1 [which is related to water flux J1 per unit membrane area by J1 = K1(Δp - ΔII)/ΔX, where Δp is the pressure difference, ΔII is the osmotic pressure of feed solution, and ΔX is the membrane thickness] of homogeneous ionic polymer membranes in reverse osmosis and their salt rejection Rs [which is given by Rs ≡ 1 - (C2″/C2′), where C2′ is the concentration of the salt in feed solution, and C2″ is the concentration of salt in effluent] were examined with cationic and anionic membranes of block and graft copolymers. For ionic membranes, Rs and K1 are related by K1 = A exp { - BRs}, where A and B are constants. This equation was found to be independent of the ion charge, the chemical nature of the polymer, and film morphology. The principle of salt rejection by ionic membranes was explained by the difference in the transport volumes (volume elements available for transport) for mobile co-ions and water. The electric repulsive force between a fixed ion and a mobile co-ion decreases the transport volume of the latter, thus creating a transport depletion of salt flux relative to water transport. This transport depletion is governed by the amount of water sorbed by a fixed ionic site, which also determines the water flux. Consequently, Rs and K1 for ionically charged membranes are related as described above. This relation significantly differs from that found between Rs and K1 for nonionic polymer membranes, where the size and the solubility of ions in the membrane are mainly responsible for the transport depletion. The decline of Rs with increasing K1 is much less in ionic membranes than in nonionic ones; however, in the high Rs region, K1 for both ionic and nonionic membranes become similar as the dominant mode of water transport changes from flow to diffusion.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 57
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1719-1724 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 58
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1729-1745 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Atactic, isotactic, and optically active poly(propylene oxides), PPOx, were irradiated with both γ-rays and electron beams. Up to a dose of 37 Mrad no change could be detected in the optical activity. G values for hydrogen evolution decreased as compared to polypropylene in about the same ratio as G(H2) of polyoxymethylene decreased as compared to polyethylene. G values for crosslinking and scission, estimated by means of gelation theories of Saito and Inokuti, were found to be greater for isotactic than for atactic PPOx. The behavior of transient infrared and ultraviolet absorption bands is discussed. Intrinsic viscosity data indicate a rapid initial chain degradation whereas CO gas and OH group production is linear with dose. Evidence for the conversion of one type of free radical to another on heating an irradiated sample from 77°K to room temperature is based on the behavior of transient infrared and ultraviolet absorption bands.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 59
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1839-1850 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Steady flow and dynamic viscosities were determined for symmetrical linear and starbranched block copolymers of butadiene and styrene above their upper (polystyrene) glass transition. Block structures examined were B-S-B, (B-S-)3, S-B-S, (S-B-)3 and (S-B-)4. At constant molecular weight and total styrene content viscosities were greater for polymers terminating in styrene blocks, irrespective of branching. Branching decreased the viscosity of either polybutadiene-terminated or polystyrene-terminated block polymers, compared at equal Mw. However, comparisons at equal block lengths showed that the length of the terminal blocks, not the total molecular weight, governs the viscoelastic behavior of these polymers to a surprisingly good approximation. This unusual result is rationalized in terms of the two-phase domain structure of these polymers, which persists to a significant degree in the melt. Below the glass transition of the polystyrene blocks the effects of branching were masked by differences in the morphology of the domain structure unrelated to branching.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 60
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1911-1914 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 61
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1977-1989 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystallinity of poly(β-benzyl L-aspartate) is highly variable, in a series of specimens prepared under various conditions: films cast from chloroform solutions at various evaporation rates, films cast comparatively slowly from chloroform-trifluoroacetic acid solutions, films prepared from dichloroacetic acid solution by treatment with ethyl alcohol, precipitates formed from trifluoroacetic acid solution by addition of ether. Film cast slowly from chloroform is in the highly crystalline ω form. In contrast, the conformation of the benzene rings in the ω helix obtained from the α helix by heating is distorted to some extent in comparison with the structure of the highly crystalline ω form. Crystallization and conformational changes from the α to the ω form, and from the ω to the β form upon heating, are correlated with the dispositions of the side chains, the packing of the benzene rings, and the motion of the side chains. The main chain of the α helix is distorted into the ω form when its side chains are in a favorable conformation. The α helix is stable in the disordered conformation, and it is distorted to some extent at high temperature.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 62
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2023-2032 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Oriented films of poly(γ-benzyl L-glutamate) (PBLG) were prepared by two methods. Films of PBLG cast from chloroform solutions were elongated by rolling at 70°C. A solution of PBLG in methylene bromide was placed in a magnetic field of about 7000 gauss and the solvent was slowly evaporated for a few days until an oriented film was obtained. The real and imaginary components of the complex piezoelectric strainconstant d25* = d25′ - jd25″ were determined over the temperature range from -180°C to +180°C at a frequency of 20 Hz. The constants showed dispersions at about 20°C and about 100°C, where dynamic viscoelastic dispersions were also observed. Degree of crystallinity Xc and degree of orientation IIa of crystallites were determined from x-ray diffraction diagrams. The product XcIIα and the value of d25′ at room temperature were found to be linearly related, and both showed a maximum at an elongation ratio of 1.5 (the ratio of the final to initial length) for roll-oriented films and at an initial solution concentration of 15% by weight for magnetically oriented films. The largest values of d25′ were approximately 2 × 10-12 and 4 × 10-12 coulomb/newton, respectively, at room temperature.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 63
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2095-2097 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 64
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2111-2117 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The two types of radicals trapped in γ-irradiated poly(ethylene 2,6-naphthalene dicarboxylate) (PEN 2,6) have been identified by ESR as —O—CH—CH2—O— (radical I) and a radical located on the naphthalene ring (radical II). The relative concentrations of radicals in the gross polymer are 10-20% radical I and 80-90% radical II. Similar trapped radicals have been identified in γ-irradiated poly(ethylene terephthalate) (PET), a structurally related polymer which differs only in the aromatic moiety, but the relative radical concentrations are quite different. These results are discussed in relation to the radiation resistance of the two polymers.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 65
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2253-2254 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 66
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 801-814 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of temperature and strain rate on the compressive yield behavior of polystyrene is compared with the effect of the same variables on crazing in tension. The results support the conclusion of other, more extensive work, which shows that crazing involves the same types of molecular processes as those which occur during deformation under compression and shear. An improved method of measuring compressive stress-strain curves is then described, and the compressive yield stress is also compared with an extrapolated tensile yield stress. The difference between the two is in line with concepts which assume a dependence of yield stress on the state of hydrostatic tension (or compression). It can be adequately described by the Mohr-Coulomb yield criterion. Application of this criterion also enables a theoretical stress strain curve in tension to be derived from other results in compression. Comparison of the tensile stress-strain curve so obtained with those which can be directly measured with other plastics, supports the hypothesis that crazing is favored by a marked decline in engineering stress during tensile elongation (plastic instability).
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 67
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 887-893 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: To determine whether the large differences in adhesion for polyethylene coatings applied to different types of copper surface could be attributed to changes in work of adhesion or wettability, the variations of contact angle with time has been measured for molten polyethylene droplets on these surfaces. It is concluded from these measurements that the low peel strengths obtained on certain substrates cannot be accounted for by a low work of adhesion of poor wetting of the surface.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 68
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 927-937 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Stress-optical coefficients have been determined for crosslinked samples of polyethylen (PE) and polystyrene (PS) at high temperatures, i.e., in the rubberlike state, and when swollen in a variety of liquids. For PE, swelling liquids with long straight molecules gave large values of optical anisotropy whereas liquids with more symmetrical molecules gave minimum values, as found previously for cis- polyisoprene and trans-polyisoprene. This solvent effect is attributed to short-range orientational order in molecularly asymmetric media. Sizes of the equivalent random link for unperturbed molecules of these three polymers were deduced from the minimum values of optical anisotropy. Measures of shape asymmetry were also obtained by matching the optical anisotropy of samples when unswollen with that observed when swollen with a liquid of known molecular asymmetry. Reasonable agreement was found to hold between the two methods. In contrast, the optical anisotropy of swollen PS was found to be substantially independent of the swelling liquid. The apparent absence of a molecular ordering effect in this case is attributed to the bulky nature of the PS molecule. A marked reduction in optical anisotropy on swelling is ascribed to increased phenyl group motion.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 69
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 999-1024 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Electron spin resonance spectroscopy has been used to study the effects of 15 MeV electrons, x-rays, and ultraviolet radiation on poly-4-methylpentene-1 (TPX) both at 77°K and at room temperature. At least seven identifiably different paramagnetic species are observable in unstabilized oxygen-free TPX after irradiation, and additional species exist in the stabilized grades. The species which predominates under most conditions is interpreted as being due to the loss of hydrogen from a main-chain tertiary carbon atom; interpretations of most of the other species are also given. Oxygen is found to diffuse rapidly into the polymer and to react with the free radicals to form peroxy species. In the absence of oxygen the radiation damage is expected to lead ultimately to crosslinking or double-bond formation, or with oxygen to degradation. The general nature of the free radicals produced by electron or x-ray irradiation is the same, but there are significant differences for ultraviolet irradiation. The observed spectra for irradiated TPX and their interpretations are in good agreement with the spectra and later interpretations for irradiated polypropylene, but are in less satisfactory agreement with the published papers on polybutene-1 and poly-3-methylbutene-1.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 70
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1025-1059 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Native celluloses of various biological origins, as well as regenerated celluloses were examined by electron microscopy after suitable dispersion. In all cases the specimens were found to be composed of a common filamentary unit which is rectangular in cross section and has the approximate dimensions 35 × 20 Å. It is suggested that these are the basic morphological units of cellulose; they are therefore called protofibrils. For protofibrils of regenerated cellulose it is shown that: (1) the molecular contour length greatly exceeds the protofibril length, (2) the mass of the protofibril corresponds to that of a single molecule, and (3) the protofibril length increases with molecular weight. Additionally, high resolution electron micrographs of native and regenerated protofibrils show an apparent axial texture with a periodicity of about 40 Å. From these observations and the knowledge that the molecular chain axis is aligned parallel to the protofibril axis, a model of the protofibril is deduced. The model consists of a ribbon which is pleated on itself so as to form a planar zigzag structure of rectangular cross section. This supersedes a previously proposed model of circular cross section. The structure is composed of a single folded, chain, arranged so that the short extended segments between the folds are parallel to the protofibril axis. The protofibril is thus regarded as the morphological expression of the cellulose molecule. Microfibrils and protofibrils often exhibit kinks, the angle between the kinked portions being 120°. This phenomenon is satisfactorily explained by the protofibril model and in fact provides good support for it. Finally, various properties of cellulose are considered in relation to the model. By contrast with the earlier crystalline-amorphous concepts of cellulose fine structure, it is suggested that protofibrils are completely crystalline structures, and that the properties of cellulose may be understood by considering processes that occur at the level of the protofibril as a unit.
    Additional Material: 21 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 71
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1149-1151 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 72
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1235-1241 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The literature on polymer morphology contains many studies of structural and orientation changes occurring upon uniaxial stretching of films and fibers, but it has only an occasional reference to such studies on biaxially stretched film. This paper presents data on a structural change due to simultaneous biaxial stretching up to 6 × 6 stretch ratio of quenched linear polyethylene slightly below the melting temperature. At low stretch ratios the b axis of the orthorhombic unit cell orients predominantly in the biaxial plane of stretching or film plane. At higher than 4 × 4 stretch ratio, a second crystal orientation appears which is a (110) orientation in the film plane. Differential scanning calorimetry scans show two melting peaks occurring concurrently with diffraction effects of two crystal orientations. The evidence for two populations of crystals differing in orientation are discussed in the light of current concepts of folded-chain lamellae and their fragmentation with elongation.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 73
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1-13 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: General kinetic equations for the gelation reaction of tetrafunctional amino monomer with formaldehyde are formulated according to Case's gelation theory. The ratio of the rate constant of the condensation reaction to that of the addition reaction is evaluated by applying a theoretical kinetic equation to the experimental measurements. The ratio of the rate constant for addition of an imino group to that for an amino group is also determined by combining the kinetic equation, stoichiometric relation, and expression for the gel point. The total yield of resin, the yield of sol, and the number-average molecular weight of the sol fraction are discussed.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 74
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 43-57 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Extinction coefficients of the characteristic infrared bands due to isomeric structural units were measured for polybutadiene and polyisoprene in CS2 or CCl4 solutions and were compared with the isomer composition determined by NMR. The NMR signal assignments were made on the basis of the spectra of deutero derivatives of the polymers. In the case of polyisoprene, linear relations were obtained between the extinction coefficients and the isomer contents determined by NMR for the absorption bands at 1385 cm-1 (characteristic of trans-1,4 units), 1376 cm-1 (cis-1,4 units), and 889 cm-1 (3,4 units). However, for the absorption bands at 840 cm-1 (characteristic of cis-1,4 and trans-1,4 units), isomerized polyisoprenes did not give such a linear relationship. In polybutadiene, the extinction coefficient for the atactic 1,2 units was found to be lower than that of the syndiotactic 1,2 unit. These experimental facts lead to the conclusion that additivity of the extinction coefficients does not always hold for diene polymers. The deviation from the linear relation may be associated with regular sequences of one isomeric conformation in the chain.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 75
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 115-126 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The apparent specific volumes, φ2, of a series of poly(propylene glycol) and poly(ethyleneglycol) oligomers in aqueous solution were determined as a function of temperature from 4 to 25°C. The slope, dφ2/dT, was taken as a measure of the extent of interaction between the hydrophobic portions of the oligomer and water, higher values of dφ2/dT representing diminished hydrophobic interaction. It is suggested that the observed increase in dφ2/dT with chain length for the poly(propylene glycol) oligomers can be attributed to the previously proposed disk coiled conformation of the chain which reduces the degree of contact between the side-chain methyl groups and water as the chain length increases. This interpretation is supported by (1) the direct relationship between the difference in the thermal expansion behavior of the two oligomer series and the accessibility of the methyl groups in the poly(propylene glycol) disk-coil, and (2) the agreement between the calculated volume changes on mixing for the methyl groups and the values predicted for the disk-coil model from the Némethy and Scheraga theory.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 76
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 175-179 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Equilibrium melting points in trans-1,4-polyisoprene were calculated from plots of crystallization temperature versus the experimentally measured melting points. The melting points were found to be 78 ± 1.7°C for the low-melting crystalline form and 87 ± 1.3°C for the high-melting form. Within the experimental error, melting points were independent of molecular weight above a number-average weight of 33,000.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 77
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 267-281 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Oscillatory shear measurements have been made on a range of anionic polystyrene melts of molecular weights 1000--500,000. For M 〈 5000 the polymer chain is too short to act as a Gaussian coil and hence the compliance of the melt is very low. For 10,000 〈 M 〈 100,000 the compliance of the melt follows the Rouse model of the elasticity of isolated polymer molecules. It is necessary to use the Ferry, Landel and Williams extension of the Rouse theory for M 〉 40,000 to allow for the effect of entanglements on the complex modulus. For M 〉 200,000 the entangelment network dominates the compliance and the Rouse theory is no longer applicable.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 78
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 283-294 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements have been made of the tensile force required to pull a disk of a model viscoelastic adhesive away from an inert rigid substrate. Over a wide range of temperature and rate of deformation of the adhesive the results were found to yield a single master relation in terms of deformation rate by means of the Williams, Landel and Ferry rate - temperature equivalence for viscous materials. Thus, the strength of adhesion is due mainly to dynamic effects in the adhesive of a viscous nature, in a similar way to the cohesive strength of viscoelastic materials. This similarity is attributed to a common failure mechanism: initial failure at a highly stressed point, followed by spreading of the failure zone under local stresses which are governed by the dynamic response of a compliant material. An increase in the strength of adhesion is observed with decreasing thickness of the adhesive layer. This is also explained by the proposed failure mechanism if failure starts at a critical amount of local deformation energy, a form of Griffith's fracture criterion.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 79
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 345-362 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Under steady shear flow, the normal stress and the shear stress in both dilute and concentrated solutions of monodisperse poly-α-methylstyrenes and their blends were measured. It was confirmed that the molecular theories of Rouse and Zimm extended to concentrated solutions can explain the relation between the zero-shear normal stress coefficient and the zero-shear steady-flow viscosity for both monodisperse and polydisperse systems. Shear-rate dependence of steady-flow viscosity can be understood fairly well by the molecular entanglement concept proposed by Graessley so long as the polymer is monodisperse or the amount of the higher molecular weight component is high. However, zero-shear viscosity of blended systems cannot be explained quantitatively by the theory of Graessley. The shear-rate dependence of steady-state compliance of blended systems was also observed, and it can well be explained by the theory of Tanaka, Yamamoto, and Takano which interpreted the shear rate-dependent steady-state compliance in terms of the relaxation time spectrum and its variation with shear rate.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 80
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 377-381 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 81
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 437-451 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The long spacing of single-crystal mats of polyethylene was found to increase reversibly on addition of liquids which normally act as swelling agents. The magnitude of the increase follows the sequence of the solvent power which these liquid exhibit at higher temperatures. The increase in long spacing depends to a minor extent on crystallization conditions, such as concentration and crystallization temperature, but increases very markedly with the molecular weight of the polymer. Heat treatment reduces the amount of swelling, even in the range of low treatment temperatures which do not produce a foldlength increase, implying a reorganization of the fold surface. It is inferred that there is a layer along the fold surface which expands by swelling which in turn implies a disordered amorphous component. Nevertheless, such disordered material need not be an intrinsic consequence of chain folding, as its amount can be reduced to insignificant proportions, e.g., by taking molecules which are short but still fold. Thus both, the presence of amorphous disorder and the nonunique nature of such a disorder along the surface is demonstrated. Further implications for the fold-surface problem are discussed.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 82
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 463-482 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Several corrections possibly required for capillary flow are based on the existence of a linear relationship between the pressure drop along the capillary and the length-to-diameter ratio at a given temperature and shear rate. Recently, the appearance of nonlinearities in this relationship has created some concern as to the cause of this behavior. The occurrence and an explanation of the nonlinearities for polystyrene form the basis of this study. A narrow-distribution, low molecular weight (20,400) polystyrene was tested in eight capillaries at temperatures of 140 and 160°C to initiate the discussion of the nonlinearity in a ΔP (pressure) versus L/D (length/diameter of capillary) plot. The sample exhibits negligible extrudate swelling at all pressures which reinforces the idea that pressure is influencing the flow. The pressure dependence of viscosity is determined using the equivalent expression of the WLF equation derived from free volume theory. Justification for its use is presented. A pressure correction, representing the increased shear stress necessary for flow of the higher viscosity material, is found to linearize the ΔP versus L/D data. A narrow-distribution, high molecular weight polystyrene (670,000) is subjected to a similar analysis at 165°C by using nine capillaries. The situation is quite different, as the high molecular weight sample is not nearly as ideal as the low molecular weight polystyrene.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 83
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 531-541 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dilatometric and calorimetric studies have been made of the fusion process of linear polyethylene crystallized by stirring xylene solutions at elevated temperatures. It is shown that the melting point of the crystals increases rapidly from 139.5°C to 145°C in the crystallization temperature range of 100-103°C and levels off to 146 ± 0.5°C, provided that very slow heating rates are employed. Stirrer-crystallized samples treated with fuming nitric acid show higher crystalline contents. Comparison of their enthalpies of fusion and melting points indicate that higher molecular order along the fiber axis is associated with higher crystallization temperatures. This is in general agreement with corresponding results of other modes of crystallization. The attack of fuming nitric acid on stirrer crystals is characterized by weight-loss curves similar to those of dilutesolution crystals and bulk polyethylene. The linear molecular weight dependence on time of exposure to nitric acid suggests that the oxidation proceeds mainly from the chain ends at a constant rate for samples stirred in the lower crystallization range, but an increased rate is observed for a sample stirred from xylene at 105°C. It is suggested that the lamellar overgrowths, most evident at low crystallization temperatures, are epitaxially attached to the fiber axis, whereas the smaller crossbandings observed at higher crystallization temperatures are possibly made up of elements of chains that are only partly incorporated in the highly ordered fibrous core.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 84
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 595-607 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Previously, the angular positions of the extrema of the polarization ratio have been utilized in light-scattering studies as a method of particle-size analysis under the assumption of monodisperse, spherical particles. Since the consequences of the existing finite polydispersity on this method of analysis was not assessed, the results are questionable. This work is concerned with (1) reporting the quantitative effects of a finite polydispersity on the method of analysis, (2) pointing out previous misuse of the method, and (3) revising the method of analysis to include polydispersity and the exact Mie calculations. The method will then permit the characterization of a scattering system in terms of a modal diameter and a distribution-width parameter by utilizing prepared diagrams for a particular relative refractive index.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 85
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 633-643 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics of dissolution of five fractions of commercial poly(vinyl chloride) in cyclohexanone was studied at temperatures from 20 to 70°C. Good agreement was observed between the experimental results and equations expressing the dependence of the induction periods and the rates of dissolution on temperature and molecular weight. It was found that the apparent activation energy for the swelling process lies in the range 9-14 kcal/mole and the apparent activation energy for the dissolution diffusion process in the range 8-12 kcal/mole. The apparent dependence of activation energies on number-average molecular weight indicates that the chain ends are more important in determining the dissolution rate than the centers of the polymer chains.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 86
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 687-715 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Light-scattering and viscometric measurements on dilute solutions of five branched polystyrene polymers are reported. The data include studies in decalin as a function of temperature, including the theta temperature, and in toluene. The results for the radius of gyration and the second virial coefficient are not in accord with the two parameter random-flight model. Possible causes of this descrepancy are considered. It is shown that the intrinsic viscosity of branched chains is not uniquely determined by the radius of gyration.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 87
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 747-754 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The electronic states localized at defects in a polyene chain with alternating bond lengths have been investigated in the Hückel approximation by direct computation on large rings. The defects considered include substitutional impurities and bond distortions. None of the cases treated seem likely to be thermally activated donor or acceptor centers, but several examples of deep or shallow traps for electrons in the conduction band are found.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 88
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 779-799 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Extensive gel-permeation chromatography (GPC) results are presented which reveal in much more detail than hitherto the effects of fractionation during the crystallization of polyethylene from solution. It is suggested how these results may be used to assess the affects of fractionation on the production of single crystals. In addition the results are compared with the fractionation which would be expected assuming the crystals to be in equilibrium with the solution. It was found that the results can be explained very well on this basis. A discussion of this rather unexpected result is included.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 89
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 841-852 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The adsorption of a series of block and random styrene-methyl methacrylate copolymers on an animal charcoal and on Graphon has been studied. On charcoal, adsorption decreases with increase of molecular weight because of the inability of larger coils to penetrate into the adsorbent. An analysis is presented which requires that coils undergo considerable distortion on adsorption in pores. The adsorption of random copolymers on Graphon is also in reverse order of molecular weight; this effect may be due to particle bridging leading to the formation of interparticle “pores.” The relative affinity of the styrene and methyl methacrylate residues is different on charcoal and Graphon, respectively; on both surfaces, however, relatively few of the more active residues are required for adsorption. Block and random copolymers are adsorbed to different extents which depend on the nature of the adsorbent surface.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 90
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 867-886 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dynamic mechanical measurements were carried out as a function of temperature (-100 to + 180°C) and frequency (3.5 to 110 cps) for a series of aliphatic terpolyamides, nylon 6 and nylon 12. Effect of crosslinking with toluene diisocyanate, of absorbed water, and of frequency are used to estimate the statistical segment length associated with the α′ relaxation. The effects of variations in the aliphatic chain length in the repeating unit on the temperature of the α′ relaxation are examined by means of copolymer rules with a view to explaining the reported insensitivity of the glass transition temperature of these polymers to changes in (CH2)/(amide) group ratio. From the estimated length of the segmental motion associated with the α′ relaxation it is inferred that in a series of polyamides of the type nylon X or nylon X,Y (where X or Y = 3, 4, 5, 6, etc.) there should be a relatively small change in the temperature of the α′ transition for those polyamides having X or Y less than about 45. Experiments which are intended to establish the position of the crystalline α-γ transition are discussed.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 91
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 959-959 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 92
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 983-998 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A comparative study of the average molecular optical anisotropy 〈γ2〉 of the polyoxyethylene chain, \documentclass{article}\pagestyle{empty}\begin{document}${\rm R} \hbox{---} {\rm O}\rlap{--} ({\rm CH}_2 {\rm CH}_2 {\rm O}\rlap{--} )_n {\rm R}$\end{document} where R = CH3, H and n is the degree of polymerization of the molecule, was carried out for the different internal rotational models considered in Part I of this series. In particular, the results obtained show that the condition of interdependence between internal rotational angles of nearest-neighboring bonds increases the average molecular optical anisotropy by about 4% (n ≫ 1), compared with the case of independent rotations. This increase is much weaker than in polyethylene chains, for which it is about 20% under analogous conditions.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 93
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1097-1115 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Studies have been made of the secondary relaxation processes in the solid state of a number of polymers containing aromatic groups in the polymer chain. The polymers investigated include one, polystyrene, with the aromatic group in side-chain positions, and six high polymers in which phenylene rings lie in the main backbone chain. In polystyrene, wagging and torsional motions of the side chain phenyl rings give rise to a low-temperature δ-relaxation which is centered at 33°K (1.7 Hz) and which has an activation energy of about 2.3 kcal/mol. Most of the polymers with phenylene rings in the main chain exhibit a low-temperature relaxation in the temperature region from 100°-200°K. This relaxation process is centered at 159°K (0.54 Hz) in poly-p-xylylene, at 162°K (0.67 Hz) in polysulfone, and at 165°K (1.24 Hz) in poly(diancarbonate). In poly(2,6-dimethyl-p-phenylene oxide), two overlapping low-temperature relaxations are found, one in the range 125-140°K and the other near 277°K (ca. 1 Hz). The low-temperature secondary relaxation process in all of these polymers is believed to be associated with local reorientational motion of the phenylene, or substituted phenylene, rings or with combined motion of the phenylene rings and nearby chain units. For these low temperature relaxation processes, the activation energy is about 10 kcal/-mole. The temperature location of the relaxation appears to depend on the specific units to which the phenylene rings are attached and on steric and polar effects caused by substituents on the ring. In the poly-p-xylylenes the relaxation is shifted to much higher temperatures by a single Cl substitution on the ring but remains at essentially the same temperature position when dichlorosubstitution is made. The effects of water on the magnitude and temperature location of the observed low temperature relaxations, as well as the implications of the study for other polymers containing aromatic groups in their backbone chains, are discussed.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 94
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1117-1131 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The diffusive permeability of water P, which relates to diffusive flux of water under a concentration gradient of water (measured by diffusion of tritiated water), and the hydraulic permeability of water K, which relates to the water flux under a hydraulic pressure gradient are defined. For the case of diffusive transport one has P = KRT/ν1, where ν1 is the molar volume of water. The relationship between P and K was investigated as a function of hydration H, i.e., the volume fraction of water in swollen polymer membranes. The following characteristic features of water permeability are revealed. (a) In the lowhydration region (H 〈 0.2), water permeates by diffusion even under an applied hydraulic pressure gradient and KRT/ν1 = P. (b) In the higher hydration region KRT/ν1 is greater than P, and the ratio ω = KRT/ν1P increases nearly exponentially with decrease of (1-H)/H. Water in this region moves partly by bulk flow under an applied hydraulic pressure gradient but moves only by diffusion in the absence of a pressure gradient. (c) The dependence of log P on (1-H)/H is nearly linear in regions of both high and low hydration but the slopes are different. The transition occurs in about the same H range where the discrepancy between P and KRT/ν1 becomes significant. Excellent agreement was found between the experimental data for P as a function of H and the theoretical prediction based on the free-volume concept of diffusive transport in hydrated homogeneous membranes.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 95
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1191-1217 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Infrared dichroism is employed to study the orientation of chain molecules in linear and ethyl-branched polyethylene in the crystalline and noncrystalline regions during drawing and subsequent annealing. A crystalline (1894 cm-1) and a noncrystalline (1368 cm-1) band, as well as the bands at 909 cm-1 and 1375 cm-1 resulting from vinyl endgroups and methyl endgroups and sidegroups, are studied. For these bands relative orientation functions are derived and compared as a function of draw ratio and annealing temperature. It is shown that the relative orientation functions as derived from the dichroism of the noncrystalline, vinyl and methyl bands follow the same curve while the orientation function for the crystalline bands does not. These results support a two-phase model for partially crystalline polyethylene and additionally favor segregation of the endgroups and sidegroups in the noncrystalline component during crystallization. It is further shown that shrinkage occurs at the temperature at which the noncrystalline chain molecules start to disorient. From the dichroism of the methyl groups in ethyl-branched polyethylene, a value for the mean orientation of the noncrystalline chain molecules is calculated. We obtain for the orientation function of the noncrystalline regions at highest draw ratios (λ = 15-20), f = 0.35-0.57, while the chain molecules in the crystallites are nearly perfectly oriented (f ≈ 1.0). On the assumption that the noncrystalline component consists of folds, tie molecules, and chain ends, the different contributions of these components to the overall orientation are estimated. From these the relative number of CH2 groups incorporated into folds, tie molecules, and cilia can be derived. Further, on the basis of a simple structural model, the relative number of chains on the crystal surface contributing to the different noncrystalline components and their average length are estimated.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 96
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1271-1285 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The viscoelastic behavior of two different ethylene-propylene copolymers was studied as a function of the molar ratios of the components and the distribution of the lengths of the ethylene and propylene sequences. The glass transition temperatures Tg agree with the values calculated from relations between Tg and component ratio established by other authors. The copolymer with longer ethylene and propylene sequences was found to exhibit a relaxation spectrum with a slope less steep than -0.5. This broadening is explained by the broader distribution of friction factors of the statistical segments in this copolymer and by differences in crystallike nearest-neighbor packing.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 97
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1325-1332 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The glass transition temperature Tg of partially sulfonated polystyrene has been measured dilatometrically as a function of degree of sulfonation. A semitheoretical relationship between Tg and degree of sulfonation has been derived by treating the strong-acid polymer as a highly polar copolymer of styrene and styrenesulfonic acid. The Tg of copolymer has been found to increase linearly up to 0.15 weight fraction of styrene-sulfonic acid wA as given by: \documentclass{article}\pagestyle{empty}\begin{document}$ T_g = T_{gB} + 200w_A $\end{document} where TgB is the glass transition temperature of loosely crosslined (1%) polystyrene matrix. Our experimental results agree well with theoretical relations developed on the basis of the iso-free-volume state of glass transition applied to sulfonated polystyrene. The marked linear increase in copolymer Tg with the styrenesulfonic acid is accounted for by the effect of progressively higher intermolecular forces due to the highly polar sulfonic acid substituents.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 98
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1345-1369 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of molecular organization (crystallinity, orientation) on the internal friction of poly(ethylene terephthalate) was studied by means of dynamic mechanical measurements at temperatures from 300 to 4.2°K, with a free-oscillating torsion pendulum at 1 Hz. It was found that crystallinity decreases the intensity of the composite γ relaxation at 210°K and gives rise to an additional loss maximum ε at 26°K. Uniaxial orientation broadens the γ relaxation and gives rise to an additional loss peak δ, at 46°K. The δ and ε losses are dependent on molecular organization, occurring only in samples containing aligned, taut chain segments and crystalline structures, respectively. They have a common activation energy of 4 kcal/mole. All three low-temperature relaxations in oriented specimens show pronounced directional anisotropy, which, in the γ loss, may be due to the preferred orientation of noncrystalline chain segments, while in the δ and ε losses, may be associated with the direction of defect structures. On the basis of the observed behavior of the δ and ε relaxations it is suggested that they may involve motions of defect structures and may thus participate in stress-transfer mechanisms at large deformations.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 99
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1399-1415 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new theory of deformation and strain induced crystallization of network polymers has been developed. The effects of lattice vacancies, variation in distribution of trans and gauche bond conformations in stretched amorphous polymers, and the crystallite orientation in the partially crystalline stretched vulcanizate were considered in the evaluation of their partition functions. Stress-extension ratio relationships were evaluated for the amorphous and semicrystalline polymers. The rise in melting temperature due to strain induced crystallization is discussed. The new theory seems to be in closer agreement with the actual strain-induced crystallization process than earlier research.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 100
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1509-1515 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Methyl acrylate, CH2CHCOOCH3, has been crystallized, and x-ray data have been collected at -120°C. The crystals are orthorhombic, space group Pnma, with four molecules in the unit cell. The structure has been determined by using symbolic addition procedures, and refined to a final residual R factor of 0.10. The molecule is planar, and the intramolecular bond distances and angles are in good agreement with values obtained for the liquid monomer by electron diffraction techniques. Considerations of crystal geometry indicate that the packing hardly permits dimerization or polymerization of the molecules in regions of crystal perfection.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...