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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 387-394 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It is proposed that bending of solution-grown polymer crystals causes the observed diffraction line-broadening in many cases. Independent estimates and observations of the severity of bending which can be sustained are used to calculate corresponding apparent crystal sizes, where the apparent crystal size is that obtained when it is assumed that broadening is caused by the small crystal size effect only. Bending broadening is found to be of sufficient magnitude to produce the observed broadening reported in the literature. Some of the steps taken so far in the development of line-broadening analysis for polymer crystals show similarities with the evolution of line-broadening analysis for graphitic carbons and a brief review of the latter is included.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 431-441 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The solid-state synthesis and properties are reported for a new polydiacetylene: poly[1,6-di(N-carbazolyl)-2,4-hexadiyne]. The monomer crystals polymerize quantitatively with γ irradiation or thermal annealing. An Autocatalytic effect is observed in both γ-ray polymerization and thermal polymerization and is attributed to an increase in chain propagation length at about 5% conversion. The activation energy for thermal polymerization is about 25 kcal/mole, independent of the degree of conversion to polymer. The exceptional thermal stability of the polymer crystals allowed a thermomechanical analysis over a large temperature range, -50 to 300°C. With increasing temperature, the polymer contracts in the chain direction linearly with temperature over the entire range, yielding a thermal expansion coefficient of (-2.32 ± 0.02) × 10-5°C-1. Photoconductivity action spectra are reported for the polymer crystals. The energies for the photoconductivity onset (ca. 2.3 eV) and for the lowest energy optical transition (1.89 eV) are the lowest reported for the polydiacetylenes. The photoconduction onset is blue-shifted with respect to optical absorption - a result which is consistent with the excitonic assignment for the lowest energy optical transition in the polydiacetylenes.
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 485-500 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Macromolecular chain rupture occurring during tensile deformation of semicrystalline polymers has been investigated by measuring changes in the viscosity-average molecular weight. When interpreted in terms of a random-scission scheme, the observed changes in molecular weight correspond to chain rupture concentrations β ≈ 1018/cm3 for high strength nylon and poly(ethylene terephthalate) fibers. Polypropylene fibers and isotropic samples of polyethylene, polypropylene, and nylon 6 had β ≈ 1016/cm3. The effects of stretching environment and thermal and mechanical history were noted. In all cases, the present study indicated bond rupture concentrations about 10 times larger than those obtained from electron spin resonance (ESR) experiments. The relation between viscometry, ESR, and infrared (IR) estimates of bond rupture and their relevance to mechanical properties are considered.
    Additional Material: 7 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 529-543 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The piezoelectric effect in films of polyvinylidene fluoride (PVF2) is investigated using optical and ultrasonic detection techniques. From the analysis of the vibrational resonance frequencies of a freely suspended film we conclude that the polarization induced in PVF2 is inhomogeneous across the volume of the sample. Poling the foils in a sandwich configuration or using blocking electrodes, we can clearly demonstrate that the piezoelectric effect in PVF2 originates from the positive metal electrode. Monitoring the time dependence of the piezoelectric effect during the poling process, a fast and slow component are observed. Using a blocking electrode, however, the same dynamical poling behavior is found only if the contacting metal electrode is positive. In view of these observations, which clearly demonstrate the importance of the metal-polymer interface for the strong piezoelectricity of PVF2, the existing theoretical models, based on the bulk properties of the polymer, are critically reviewed.
    Additional Material: 10 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 501-511 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A previous study of poly(ethylene oxide) (PEO) in aqueous salt solutions has been extended to incorporate cloud-point measurements in potassium thiocyanate solutions (salt concentration range 3.3-3.8M where salting out occurs) and, particularly, viscosity measurements. A few osmoticpressure measurements were made and molecular weights (∼2 × 104) from gel-permeation chromatography (GPC) compared. The theta temperature for PEO in water from cloud points was found to be 369 ± 3°K. An empirical linear relation has been found for sodium and potassium salts between the finite change of theta temperatures with change in ionic strength, δθ/δI, and (v3 - v̄3), the difference between the molar van der Waals volume and the partial molar volume of the salt. Values of the Huggins constant k′ are less than 0.5 for PEO in pure water at 303.2°K, indicating a good solvent, whereas in salt solutions they vary from 0.59 to 1.14 in nontheta solvents. They and other findings are attributed to binding of salt to the polymer and to water structure breaking. Kraemer's constants k″ were also determined: k′ - k″ = 0.5 for PEO in pure water, and for aqueous salt solutions of PEO, k′ - k″ = 0.666 at 298°K. Values of K0(= M-1/2[η]θ) with M = 2 × 104 were found to very with salt type (valence) - mean values of 103 K0/dlg-1 with number of observations in brackets are 1:1, 1.19 (2); 1:2, 1.45 (3); 2:2, 1.75 (3). Unperturbed dimensions 〈r2〉01/2 vary from 11.0 to 12.6 nm from 1:1 to 2:2 salts. Values of the characteristic ratio Cn, the steric parameter σ, and the enthalpy and entropy of dilution parameters χH and χS have also been calculated.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 159-169 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Phenylmercurated poly(ethylene terephthalate) (PET) chain-ends are obtainable through the transesterification of PET by phenylmercury hydroxide or acetate in solution in nitrobenzene at 165 ± 10°C. The reaction results in an average of one mercury atom per chain. The phenylmercuration may be followed by infrared or x-ray fluorescence. Reaction with concentrated HCI Affords the elucidation of some structural parameters of the resultant partially crystalline tagged PET, through analyses of changes in viscosity and molecular weight, in percent crystallinity, and in the amount of mercury in the system. The chain-ends are almost completely excluded from the stem region of the PET crystal with no more than 2% remaining. The chain-ends are distributed unevenly throughout the amorphous phase. This is corroborated by sharp decreases in scattered intensity of small-angle x-ray measurements. Two models for the distribution of chain-ends in the amorphous phase are considered. The one in which the ends are pushed farthest from the crystal surface and concentrate halfway between crystallites is tentatively adopted. Analysis of the HCI hydrolysis kinetics and products leads to the following picture concerning the fold tightness and position. About one out of five folds extends significantly into the amorphous matter where it is mingled with cilia, tie molecules, and unattached molecules. Random scission throughout such an amorphous mass should lead to a preponderance of cleaved molecules whose length should be four to five times the lenght of the crystalline stem region, as is indeed observed.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 759-766 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Characterization measurements of a commercial phenol-formaldehyde resin prepared from constituents including phenol and formaldehyde in the molar ratio 1:1.33 are reported. The measurements consist of (1) the linear thermal expansion coefficient between approximately 85 and 270°K; (2) the specific heat capacity between approximately 6 and 100°K; (3) the Young's modulus at room temperature. A critical examination of the data reveals that: (1) the vibrational behavior is predominantly that of a three-dimensional assembly; (2) as far as data available from other sources permit an assessment to be made, the principle of additivity appears to be applicable to the specific heat capacity between approximately 50 and 100°K; and (3) the data lie near the limit of an empirical relationship observed between the Young's modulus and linear thermal expansion coefficient of other polymers.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 427-430 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Radiothermoluminescence has been used to show that the surface of latex globules in nonvulcanized latex films contain segments which become mobile at a temperature 20°K below that observed in bulk polymer. Vulcanization in latex films takes place mainly on the surfaces of the latex globules; vulcanized latex films are microheterogeneous systems.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 457-466 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Smoluchowski formalism is used to solve the problem of a bead of frictional resistance β attached to a surface with a spring of force constant k over which a linear shear field of strenght α flows. The power dissipation is given by βα2kT/k. k and T have their usual meanings. The result is generalized to an n-bead polymer. It is found that the power dissipation of a Rouse model polymer attached to a surface at one end is twice that of an identical polymer flowing freely in solution. If the force constant k arises from an entropy force, then, because of the effect of the surface on the number of polymer configurations, there is an additional factor of two. The same relationship is expected to also hold for the frequency-dependent power dissipation. It is argued that a net circulation exists in the beads above the surface and that the magnitude of the circulation is roughly comparable to that which exists in a polymer freely rotating in solution under a shear field of the same magnitude.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 523-528 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: By measurement of integrated intensities of high-resolution proton nuclear magnetic resonance (NMR) bands, associated structures of isotactic (i) and syndiotactic (s) poly(methyl methacrylate) (PMMA) in dilute toluene-d8 and dimethylformamide-d7 solutions were detected and characterized. In 1% (w/v) solutions of highly stereoregular s-PMMA in toluene-d8 at 27°C, 76% of the monomer units are present in the form of compact aggregates. Consequences of this finding for the polymerization of methyl methacrylate in toluene in the presence of s-PMMA are discussed.
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  • 11
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 555-564 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A theory of variability in lifetimes of identical polymer specimens under identical test conditions is formulated, using the theory of fracture of amorphous crosslinked polymers developed previously by the authors. Variability in fracture times follows from the assumption that the critical number Ncr of bonds that must fail in order to cause fracture of a specimen varies from specimen to specimen. A plausible physical explanation for the variation in Ncr may well lie in the variability of the spatial distribution of weak local regions. The scale of locality may vary from molecular to grosser dimensions. The theory is applied to styrene-butadiene rubber (SBR) under creep conditions and fares well in its prediction of observed results. Most notably, it predicts that the shape of the distribution curve of the observed lifetimes remains invariant with changes in the levels of stress and temperature and that the effects of these manifest themselves through shifts of the curve on the logarithmic time axis. The theory also predicts correctly that the fracture process is accelerated if the creep test is interrupted by unloading-reloading cycles at high strain rates. This last result is shown to be a direct consequence of the concept of “the endochronic time to fracture,” previously introduced by the first author.
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  • 12
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 599-612 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Morphological changes accompanying the deformation of polypropylene filaments with varying degrees of melt-induced orientation are examined using wide-angle x-ray scattering (WAXS), small-angle x-ray scattering (SAXS), and electron microscopy, and their behavior is compared both to completely unoriented film samples and to very highly oriented, hard elastic filaments. Melt-oriented filaments are shown to deform predominantly by a voiding mechanism at low temperatures (〈100°C), and destruction of the lamellas to produce fibrils occurs only after extensive drawing. The bimodal crystal texture of the filaments does not appear to greatly affect the low temperature deformation mechanism. High temperature (〉100°C) drawing produces a fibrillar structure containing elongated voids.
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  • 13
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 667-678 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Three of the Poisson's ratios have been measured on a low-density polyethylene (LDPE) sheet with parallel lamellas morphology over the temperature range from +20 to -60°C. The measurements were carried out using a specially constructed lateral extensometer which utilized the Hall effect to detect the very small strains involved. The Poisson's ratios show considerable temperature dependence, and at high temperature the overall deformation approximates to pure shear as previously noted. It is suggested that this relates to the onset of the c-shear relaxation.
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  • 14
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1297-1319 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The load-elongation behavior during the postneck drawing stage in the deformation of crystalline polymers is shown to be modeled quantitatively by an aligned short-fiber composite in which crystalline fibrils form the reinforcing phase in a matrix of less well-ordered material. Three modes of deformation are distinguished in the model and are shown to correspond to the observed loadelongation relations in polyethylene and polypropylene. The regions are (I) elastic-plastic crystals in an elastic matrix, (II) elastic-plastic crystals in an elastic-plastic matrix, (III) elastic crystals in an elastic-plastic matrix. A requirement of the theory is that the flow stress in the crystals is little affected by temperature whereas that in the matrix falls as the temperature rises. Expressions are given for stress in terms of the applied strain and the relevant parameters of the system: concentration of fibrils, length and diameter of fibrils, and elastic and yield properties of fibrils and matrix.
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  • 15
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1365-1379 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The four-center solid-state photopolymerization of distyrylpyrazine (DSP) and of 2,6-naphthalene bis(acrylic acid-2,4-dichloro phenyl ester) (NBA-DCP) was investigated by x-ray and microscopic techniques. In both cases the polymer grows as a separate product phase topotactically well arranged with respect to the monomer matrix. In the case of polymerization of DSP the space group of the monomer (Pbca) is not maintained but the polymer phase has space group P21ca. Nucleation and growth of the polymer phase was observed by light and electron microscopy. Nucleation occurs at defect sites. The polymer grows at different rates in different crystallographic directions which were identified by electron diffraction in the case of DSP. Polymerization thus occurs in the transition region between monomer crystal and product phase and not in the bulk of the crystal so that the four-center-type photopolymerization is best described as a heterogeneous solid-state reaction.
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  • 16
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 171-177 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Preferred orientations have been observed for polyethylene single crystals deposited at room temperature on a clean polyethlene substrate crystal or a polyethylene substrate crystal coated with silicone oil (but not with a carbon layer). The observed angular relationships can be explained in terms of a network of interfacial dislocations, the cores of which lie in the fold regions between the crystals, and the long-range strain fields extend into the lattices of both crystals. The interfacial dislocations seem likely to result from the plugging of cilia from one crystal into another.
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  • 17
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 215-222 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Treatement with hydrazine was used to investigate the crystalline morophology of commercially drawn nylon 6,6 fibers. Electron microscopic investigation revealed a stacked lamellar structure for the debris of a highly oriented, rapidly drawn fiber. However, the high molecular weight range of the gel permeation chromatogram of this same oriented fiber indicated the presence of high molecular weight material. This is thought to be due to the production of rod-like, partially extended regions during drawing.
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  • 18
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 297-318 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Diffusion of five polystyrene fractions at various concentrations in toluene through cellophane membranes has been observed. The results have been used to calculate friction coefficients between solvent and solute, and between solute and membrane. The calculation requires measurement of the diffusion coefficient and the reflection coefficient of the solute, of the permeability for the solvent, of the pore volume of the membrane, and of the partition coefficient of the solute between membrane and solvent. By comparing the friction coefficient between solvent and solute in the membrane with this coefficient in free solution, the tortuosity factor and the pore diameter of the membrane can be estimated. The dependence of the friction coefficients on molecular weight M2 of the solute is determined. For large values of M2, the friction between solute and solvent is the determining factor. The friction coefficient between solute and solvent increases more strongly with M2 in the membrane than in free solution owing to an entrance effect for the permeating solute at the interface.
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  • 19
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 371-374 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 20
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1-11 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dielectric behavior of a low molecular weight fraction of poly(diethylene glycol terephthalate) has been studied over the frequency range 102 to 105 Hz for temperatures between -67 and +51°C. Two relaxations, α and β, which exhibit pseudoactivation energies of 52 and 8 kcal/mole, respectively, have been found. The α relaxation, associated with the glass transition of the polymer, is amenable to a Williams-Landel-Ferry (WLF) analysis. The dipole moment ration 〈μ2〉/Nm2 (where 〈μ2〉 is the mean square dipole moment of a chain consisting of N bonds and m2 is the average of the squares of the bond moments) has also been calculated using the dielectric data obtained for the polymer in the undiluted state. The calculations yield 〈μ2〉/Nm2 = 0.710, a value in very good agreement with that obtained from measurements in solution.
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  • 21
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 569-581 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A butadiene, styrene, 4-vinylpyridine terpolymer has been crosslinked by coordination of the pyridine groups with iron chloride. The distribution and structure of the iron complexes have been studied. Electron microscopy has given evidence of clustering of the iron complexes. The size distribution of these clusters has been evaluated by small-angle x-ray and neutron scattering. Mössbauer spectroscopy and magnetization measurements have shown the presence of three different kinds of iron complexes: (a) complexes with a speromagnetic structure in the clusters previously found, (b) dimers with antiferromagnetic coupling, and (c) quasi-isolated complexes with weak ferromagnetic coupling. The percentages of these different iron complexes have been measured.
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  • 22
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 641-651 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dielectric behavior of maleic acid-ethylene copolymer solutions has been investigated at different polymer concentrations and two degrees of neutralization α′. It is shown that this behavior is analogous to that of ordinary polyacids. Also the experimental data can be explained in terms of the van der Touw-Mandel theory, but at low α′ a possible contribution from motion of negative charges (in turn related to bound proton fluctuations) has to be taken into account. The dielectric results suggest that the formation of intramolecular hydrogen bonds has an influence on the change of the average dimensions of the chain with increasing α′. This seems to be confirmed by viscosity data.
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  • 23
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 813-820 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In-service secondary creep rates of natural rubber (NR) vulcanizates at ambient temperature are known to be low. However, in tests on thin strips of NR vulcanizates in tension, secondary creep at rates of up to 120%/week were observed. From an examination of the effect of antioxidants, antiozonants, waxes, and specimen thickness it was shown that the anomalous creep was due to ozone attack on the vulcanizate, which only becomes serious in tests on thin strips in tension.
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  • 24
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 851-858 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A detailed description of the synthesis of a model poly(isoprene-g-styrene) is given. From light scattering measurements the real radius of gyration of the polyisoprene is backbone is found to be smaller than that of the polystyrene branches. The core-and-shell conformation of graft copolymers in dilute solution in good solvents, which was proposed for poly(styrene-g-isoprene), is supported by these results.
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  • 25
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 895-906 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of low-molecular-weight linear polyesters were epitaxially crystallized from dilute solution and the melt on a variety of organic and inorganic substrates. The rod-like polyester crystals which were formed assumed general orientations in alignment with substrate geometry. This yielded monodirectional orientation of these crystals on one of the organic substrates, and bidirectional orientation on the other surfaces. Heterogeneous nucleation on the organic substrates, trioxane and naphthalene, induced the growth of much larger epitaxial crystals than have previously been observed on inorganic substrates. Those polyesters, with a high percentage of methylene units per chain repeat, crystallized in an unusual polymorphic form when in contact with the organic substrates. Polymorphic transformation to the normal form was not possible under thermal treatment or with increased crystal thickness. The expected relationship between dipolar alignment in the polymer crystal and this polymorphism was established.
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  • 26
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 967-970 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Relations are derived for the linear and volumetric thermal expansion coefficients of a filled polymer containing aligned ellipsoidal inclusions at finite concentrations. The analysis follows a procedure recently developed for elastic moduli by application of a generalized approach of Eshelby. The well-known Kerner equation is shown to be a limiting case of the present finding. From data on glass in epoxy resin, we conclude that the volumetric expansion varies only slightly with the aspect ratio of an ellipsoid; however, the longitudinal and transverse, linear, expansions show a strong dependence on the particle shape.
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  • 27
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 989-998 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements of the increase in the relative permittivity for solutions of polystyrenes, poly(p-ethoxystyrene), poly(methyl methacrylate), and poly(N-vinyl carbazole) when subjected to shear gradients are reported. The influences of such factors as shear rate, concentration, viscosity, solvent permittivity, polymer dipole moment, and polymer molecular weight on the phenomenon are described. An empirical correlation for the diverse data obtained with polystyrenes and poly(p-ethoxystyrene) has been established, but this relation does not entirely match the theoretically predicted effects. We discuss the various physical processes which may have an influence on the observed phenomenon.
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  • 28
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1023-1029 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The results of extended Huckel calculations are reported for an isolated (SN)x chain in which some of the S2N2 units of the extended one-dimensional chain are replaced by (SCH2)2 units. It is found that, inter alia, the metallic behavior of the unsubstituted parent is retained but that the conductivity is lowered to an extent governed by the nature and degree of substitution.
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  • 29
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1155-1168 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The induction period for the onset of crystallization was determined in poly(ethylene terephthalate) in the presence and absence of small metallic particles. Two kinds of substrates were used: single microcrystals “transplanted” from the water-soluble inorganic polymer (NaPO3)x and powders of the same metals (Au, Pt, and Ir). The nucleating activity φ of the substrates was determined on the basis of classical nucleation theory. Values of φ obtained for PET are compared with the corresponding values in the (NaPO3)x melt and with theoretical concepts.
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  • 30
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1219-1225 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The electron density of the polyoxymethylene molecule was calculated in cylindrical coordinates by a newly derived Fourier method. The density due to hydrogen could be obtained in addition to that from carbon and oxygen. This method is generally applicable to a helical polymer whose unit cell contains only one molecule composed of a number of chemical repeat units in the fiber identity period.
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  • 31
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1071-1084 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A model for the mechanical behavior of solid polymers is proposed in the form of a linear elastic network with transitions. A simplified version of the model involving a single column of two-site activated processes is found to be a mean-field system. The failings of this system as a description of yield and glass transition relaxation behavior lead to two extensions to the system: that of many available sites in each activated process, and that of a finite number of such processes in the whole system. These extensions reduce the properties of the system to those of a single activated flow process with a temperature-dependent activation energy. Agreement is found between this result and time-temperature shift measurements in the α transition region of several polymers, together with an explanation of the dependence of yield stress on temperature for one of these polymers that is physically more reasonable than the usual constant activation energy proposal.
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  • 32
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1135-1138 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
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  • 33
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1181-1193 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Raman spectrum of partially crystalline polyethylene can be described as a superposition of three components, which originate from the orthorhombic crystalline phase, a meltlike amorphous phase, and a disordered phase of anisotropic nature, where chains are stretched but have lost their lateral order. The mass fractions involved in the three phases can be derived directly from the integral intensities of characteristic bands without an additional calibration procedure. A comparison of the results obtained for a variety of samples shows agreement with the crystallinities derived from the density, and the small-angle and wide-angle x-ray diagrams. Data indicate that the disordered anisotropic phase is located at a transition zone between crystalline and amorphous layers. Application of the method in a temperature-dependence experiment permits a detailed examination of partial melting.
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  • 34
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1253-1260 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A complex fine structure in the C—H stretching region of the infrared spectrum of deformed polyethylene single crystals is reported. The deformed crystals are shown to be transformed from the orthorhombic crystal form to a monoclinic structure. The previously deduced C2/m monoclinic structure does not account for the appearance of the new bands. An alternative but similar monoclinic structure is proposed. The symmetry of this structure is consistent with the Fermi resonance interactions required for the observation of these bands.
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  • 35
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 49-57 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: X-ray diffraction has been used to further investigate the quenched form of polypropylene. The diffractometer traces were analyzed by a mathematical peak separation procedure which assumed a combined Cauchy and Gaussian shape for the peaks. The results confirmed that the quenched form contains about 60% of amorphous polypropylene. In the remainder, the x-ray diffraction peak positions indicate that the chain helices are arranged in a square array and a cubic or tetragonal symmetry is proposed for this phase. The shape of the x-ray diffractometer peaks indicates a degree of strain in the structure. Crystallite sizes, determined from peak breadths, have been estimated as approximately 30 Å.
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  • 36
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 105-115 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The intrinsic viscosity of a single sample of polystyrene was measured as a function of the composition of solvent in three mixed solvent pairs. The parameter Y introduced by Shultz and Flory was useful for prediction of trends, but severely overestimated the effect of solvent (1)-solvent (2) interaction on the expansion of polymer coils. The system polystyrene-cyclohexane-ethyl acetate was studied in detail for five samples of polystyrene. The analysis of the data provided strong experimental proof of a strict validity of the Mark-Houwink-Sakurada relation. The dependence of the Mark-Houwink-Sakurada exponent α on the composition of the solvent mixture was unexpectedly unsymmetrical. The unperturbed dimentions of the polystyrene chain are reduced by specific interaction of polystyrene with carbonyl groups in the solvent mixture.
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  • 37
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 977-987 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Copolymers of vinylpyrrolidone-p-tert-butylphenyl methacrylate (VP-MBPh) of several compositions were prepared by polymerization in benzene at 50°C using α′α′-azobisisobutyronitrile as initiator. Three of the copolymers were fractionated. Number-average molecular weights of fractionated samples were determined by osmotic pressure in benzene or 2-propanol. Kuhn-Mark-Houwink relations were established in benzene, chloroform, and 2-propanol. From the relation between Mn and the intrinsic viscosity (η), it appears that these random copolymers behave as predicted by the theory for flexible polymers. Abnormal viscometric behavior shown by one of the copolymers in nitromethane at 29°C (the theta temperature) is discussed. The Stockmayer-Fixman semiempirical method was used for estimating unperturbed dimensions from viscosity data obtained in chloroform, a good common solvent. Values of the viscosity parameter Kθ increase with the content of p-tert-butylphenyl methacrylate. In general, experimental Kθ values are higher than those calculated for the homopolymers. Excluded-volume parameters are estimated and discussed in relation to repulsive interactions between unlike monomer units.
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  • 38
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The storage and loss shear moduli G′ and G″ of dilute solutions of two samples of sodium poly(styrene sulfonate) with molecular weights (M) of 3.28 × 105 have been measured. The Birnboim-Schrag multiple-lumped resonator technique was used in the frequency range 100-8000 Hz, and the intrinsic moduli were obtained by extrapolation to infinite dilution. Measurements were performed over the temperature range from 1.0 to 25.0°C in aqueous solvents containing from 0 to 60% by weight glycerol and from 0.001 to 0.005M added salt. The large intrinsic viscosities indicated high extension of the polymer, and the frequency dependences of G′ and G″ were matched well by hybrid relaxation spectra combining rodlike and coil-like behavior. In a solvent containing 0.001M sodium ion and no glycerol, the end-over-end rotational relaxation times for the two molecular weights corresponded to proportionality to the 1.7 power of M. With increasing molecular weight, ionic strength, and/or glycerol concentration, the polyelectrolyte appeared to become less extended, and its behavior more nearly coil-like.
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  • 39
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 13-28 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Electrically polarized and unpolarized films of polyacrylonitrile (PAN) have been investigated by both infrared attenuated total reflection (ATR) and thermally stimulated discharge (TSD). ATR analysis of PAN films has been aimed at explaining the molecular origin of thermally stimulated currents, and consequently that of phenomena contributing to electrical polarization in this material. Preferred orientation of nitrile dipoles along the thickness direction (applied electric field direction) has been detected by ATR in both polarized and unpolarized films. It is suggested that dipolar alignment in unpolarized solvent-cast films could result from internal electric fields associated with space charges. The observed orientational anisotropy is found to disappear gradually as films (both polarized and unpolarized) are heated from ambient temperature to 100°C and rotational motion in the backbone is thermally activated. TSD currents observed in this thermal range are thus associated with randomization of molecular dipoles. TSD currents observed above 100°C are suggested to originate from drift of space charges, since both an isotropic orientation of dipoles and onset of considerable diffusion are detected by ATR in this temperature range. PAN films polarized by high-intensity electric fields (5 × 105Vcm-1, as opposed to 5 × 104Vcm-1) are found to retain orientational anisotropy above 100°C, and this is believed to be associated with a structural rearrangement induced by electrical polarization.
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  • 40
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 91-104 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A study of crack propagation in double cantilever beam specimens of polycarbonate has revealed a large velocity-dependent instability in the plane-strain fracture energy GIc. At a crack velocity of 10-2 in./min, GIc accords with published values obtained from tensile studies of precracked specimens. Crack propagation in doubly grooved double cantilever beam specimens is unstable at higher velocities. The GIc's during crack jumping and at crack arrest are estimated to be 0.2 and 2%, respectively, of the low crack speed value, based on the amounts of crazing produced at the various crack speeds. Evidence of plane-strain shear deformation at the low speed crack tip is presented. The GIc instability is suggested to arise from differences in the kinetics of shear failure and craze breakdown.
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  • 41
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 131-142 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystal structure of isotactic poly(4-methyl-1-pentene) was determined by x-ray analysis. The unit cell is tetragonal, P4b2, with α = 18.70 Å and c (fiber axis) = 13.68 Å; it contains four molecular chains each consisting of seven monomeric units in the fiber period. The molecular conformation is essentially a (7/2) helix, but deviates slightly from the uniform (7/2) helix. The unusual low density is discussed from the structural point of view.
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  • 42
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 179-188 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polypropylene was evaporated on the (001) cleavage faces of alkali halide single crystals, NaCl, KCl, KBr, and KI, under a vacuum of 10-5 torr. Films evaporated on the substrate were found to be composed of low molecular weight polypropylene with a narrow molecular weight distribution. The polypropylene film evaporated on the substrate maintained at 100°C, was composed of rod-like crystals of α form, the (010) plane of which was parallel to the (001) plane of alkali halide and their long axes were oriented in the (110) direction of the substrate. When the substrate was kept above 150°C, the film included three crystalline forms, α, γ, and δ forms. Fiber-like crystals of the α form lay parallel to the (110) direction of NaCl. In the initial stage of growth, lamellar crystals were observed in the film. The lamellar (001) plane lay flat in the film and branching occurred on the (010) lateral faces. Both the γ-form and the (predominately) new δ-form crystals were observed in the same area of the film prepared at temperatures above 150°C.
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  • 43
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 223-230 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Thermally stimulated currents (TSC) of γ-irradiated poly(methyl methacrylate) thermoelectrets have been investigated in the high-temperature range. The two main peaks of the TSC spectrum, appearing, respectively, at about 100 (α) and 120°C (ρ), show marked differences in stability under irradiation: while the α peak is little affected by doses up to 107 rad, the ρ peak vanishes following doses of 105 to 106 rad. On the other hand, a study of the rate of decrease of the ρ peak as a function of irradiation conditions reveals the important role of the surrounding atmosphere and the existence of a flux effect, probably related to irradiation-accelerated diffusion of gas into the polymer. All these facts confirm the respective attributions of α and ρ peaks to a dipolar volume polarization and to an ionic space charge polarization, showing that the TSC study of irradiated thermoelectrets can be a useful method for identification of polarization processes in polymers.
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  • 44
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 289-296 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The equilibrium melting temperature, volume, and enthalpy and entropy changes on melting of poly(ethylene terephthalate) have been analyzed and heats of fusion have been newly measured with an automated scanning calorimeter to yield the following data: 553°K, 16.9 cm3/mole, 2.69 kJ/mole, and 48.6 J/deg/mole, respectively. A more detailed discussion of annealed samples obtained from etched starting materials shows that the density of the noncrystalline regions may be variable.
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  • 45
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 335-339 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of heat treatment at temperatures above 300°C on the low temperature relaxation of poly(4,4′-oxydiphenylenepyromellitimide) (Kapton H-film) was studied by wide-line nuclear magnetic resonance (NMR), mechanical, and dielectric measurements. In the NMR line spectrum of the as-received film, a narrow component above -60°C and a broad component which begins to narrow at about -100°C were observed. It is proposed that the narrow component is associated with absorbed water, because it disappeared in the heat-treated film at 300°C in N2. On the other hand, the behavior of the broad component was not influenced by heating to 300°C in N2. Mechanical and dielectric loss peaks were observed at -75°C (11 Hz) and -65°C (1 kHz), respectively, in the as-received film. These loss peaks did not change in intensity with heating to 300°C in N2. It is proposed that the mechanical and dielectric loss peaks corresponding to the narrowing of the NMR broad component are associated with the local-mode motion of the diphenylether portion of the polypyromellitimide chain. It was found that crosslinks are formed by heating to 374°C in air through coupling of the diphenylether portions of the molecular chains. With the formation of crosslinks the dielectric loss peak shifted toward higher temperature and the intensity decreased through restriction of the local-mode motion of the diphenylether portion of the molecular chain.
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  • 46
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 349-366 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Methanol crazes are grown from sharp cracks in poly(methyl methacrylate) (PMMA). The craze thickness profile is measured using a replica technique after the craze opening displacement profile of the growing craze has been measured with holographic interferometry. The craze strain profile is then computed from these data. The craze surface stress profile is determined by two methods: (1) from the uniaxial strain profile of regions adjacent to the craze as measured from the fringe spacing on the reconstructed hologram and (2) from the craze opening displacement profile using the Fourier transform method of Sneddon. From the surface stress and craze-strain profiles a true stress-strain curve for the craze fibrils has been constructed. The extrapolated fibril yield stress is in good agreement with the yield stress of bulk PMMA plasticized with methanol indicating that surface tension effects do not contribute importantly to craze fibril mechanical properties at room temperature. The craze strain increases from 0.4 near the craze tip to 1.4 near the craze base implying that methanol crazes in PMMA thicken by further straining of the existing craze fibrils and not by drawing new material into the craze from the craze surfaces. The primordial craze thickness, i.e., the original thickness of polymer which fibrillates to form the craze fibrils, is approximately 1 μm and is constant over most of the craze length. This thickness may be determined by diffusion of methanol normal to the craze surfaces in a process zone just behind the craze tip.
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  • 47
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 407-414 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The peel strength of a joint with flexible materials bonded by an elastic adhesive was evaluated in relation to the fracture mechanism. It was found that initiation and propagation of peeling are governed by different mechanisms. Initiation (the formation of an initial crack) occurs when the maximum stress in the adhesive layer reaches a definite value. In this case, the strength fi in a trousers-type peeling is given by 2fi = y0σb∊b, where y0 is the half-thickness of the adhesive layer, σb is the tensile strength, and ∊b is the tensile elongation of the adhesive. On the other hand, propagation is governed by the surface energy of the adhesive. In this case, the peeling strength fs is determined by a balance of energies. For trousers-type peeling it is given by 2fs = Γ, where Γ is twice the surface energy. These results were verified experimentally.
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  • 48
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 415-425 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An attempt was made to study the effect of interfacial slippage on the filler reinforcement based on the boundary condition that the constituents of a particle-filled composite can slip relative to each other, but no cavities are formed at the interfaces. The elastic field satisfying these conditions is derived using the linear theory of elasticity and the effective elastic moduli of the composite are calculated. The following assumptions are made: (1) Filler particles are spherical, (2) fillers are completely dispersed, and (3) the volume fraction of fillers is sufficiently small that the interaction among fillers may be neglected. The expression for the shear modulus of the composite μ**, which is derived here, is consistent with the viscosity of a suspension which has been derived by Oldroyd. Experiments who that the increase of Young's modulus by glass beads (GB) is lower in polystyrene (PS) than in epoxy resin (Ep). The reinforcement in Ep-GB systems can be estimated by the well known formula derived assuming perfect adhesion. However, the reinforcement in PS-GB systems is in rather good agreement with the formula derived here assuming interfacial slippage.
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  • 49
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 513-521 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Kinetic studies of the pH-induced conformational transition of the hydrophobic copolyelectrolyte of maleic acid and styrene in aqueous NaCl at ionic strength 0.09 were performed by an optical method at 25.0°C with a rapid reaction analyzer of high resolving power. A pH jump applied to a solution, in which the molecule is in the compact form, gives a kinetic trace from which, by appling the general kinetic theory of cooperative transitions, two mean relaxation times are determined. Plots of these relaxation times against the degree of ionization of the primary carboxyl groups of the maleic acid units agree well with theoretical predictions from the linear Ising model, where the molecule in the compact form is described as a random coil with hydrophobic “pockets.” The initiation parameter for a pocket obtained from the kinetic data is 0.036. On the other hand, the parameter calculated from the previous pH-titration results by applying Zimm-Rice theory is 0.015 at the ionic strength 0.09 and 25.0°C. Such values are compared with those determined from pH-titration data on other hydrophobic polyelectrolytes.
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  • 50
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 545-553 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Our laboratory previously reported the observation of a high temperature, melt rheological transition in a styrene-butadiene-styrene (S:7 × 103 and B:43 × 103) block copolymer from the highly elastic, nonlinear viscous behavior typical of a multiphase structure to linear viscous behavior with insignificant elasticity typical of a single-phase structure. We have investigated the precise nature of this melt rheological transition in the 7S-43B-7S sample by measuring the dynamic viscoelastic properties at more than 11 temperatures, including several in the transition region. A new procedure was developed for accurately measuring the sample temperature in a Weissenberg rheogoniometer. The transition is found to start at about 140°C and proceed over a narrow transition region from 140 to about 150°C. Data at all temperatures superimpose onto a single master curve only at high reduced frequencies. At low reduced frequencies, two characteristic branches of the master curve are formed. The data at temperatures below the transition region superimpose onto the upper branch where the dynamic viscosity η′(ω) is a strong function of ω, whereas the data at temperatures above the transition region superimpose onto the lower branch where η′(ω) is independent of ω. The data at temperatures within the transition region fall between the upper and lower branches, ordered according to their temperature positions. The apparent flow activation energy is found to be constant at about 22.8 kcal/mole below the transition region, but appears to decrease to about 17.4 kcal/mole above the transition region. The narrowness of the rheological transition far above the glass transition temperature of the polystyrene domains and the limiting linear viscoelastic behavior at low frequencies above the transition suggest an accompanying morphological transition rather than a gradual weakening of the polystyrene domains.
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  • 51
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 583-597 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Millar-type interpenetrating polymer networks (IPNs) are composed of two identical networks. In the present case Millar IPNs of polystyrene/polystyrene were prepared where the crosslinker levels of the two networks differed by a factor of 10. Polymer network I contained 0.4% divinylbenzene (DVB) and polymer network II contained 4% DVB, the polymers having the following weight proportions: 75/25, 50/50, and 25/75. A single polystyrene network containing 2.2% DVB was synthesized for comparison with the 50/50 Millar IPN, both containing the same average amount of crosslinker. The creep behavior of the Millar IPNs was found to be dominated by polymer network I, as were the rubbery moduli and swelling behavior in toluene. These results suggested that polymer I domains are more continuous in space and polymer II domains are less continuous. The Donatelli equation predicted polymer II domain sizes of 60 Å to 100 Å for the Millar IPNs. Electron micrographs of specimens containing 1% isoprene in polymer II offered visual evidence for the segregation of polymer II domains from polymer I, and showed that the polymer II domains were, in fact, less continuous. Polymer II domains varied from about 50 to 100 Å in size, as predicted. These results have implications for gelation processes in general.
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  • 52
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 653-665 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Adam-Gibbs molecular theory, which describes the temperature dependence of relaxation phenomena in the main transition region in terms of the configurational entropy of a system, has been extended to include the effect of concentration of a low-molecular-weight compound on the viscoelastic behavior of concentrated polymer solutions. The concentration dependence of relaxation times in the polymer-diluent mixture leads to an expression of the concentration dependence both of the shift factor in the Williams-Landel-Ferry (WLF) equation and of the glass transition temperature Tg of the mixture. The constants of the WLF equation and the concentration dependence of Tg are given in terms of a difference between the specific heats of the liquid and glass ΔCp of the equilibrium temperature T2 of the second-order transition, and of the parameter Δμsc*/k, which includes the chemical potential Δμ and the configurational entropy sc* of the smallest cooperatively rearranging region. The resulting relationships also predict the temperature dependence of the constants of the concentration WLF equation. Good agreement was found between theory and the viscoelastic and Tg data on the systems poly(vinyl acetate) + diethyl phthalate, poly(methyl methacrylate) + diethyl phthalate and polystyrene + dibutyl phthalate. This finding indicates that the configurational entropy, at least in the first approximation, is responsible for the concentration dependence of relaxation phenomena in concentrated polymer solutions.
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  • 53
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 613-625 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Small-angle x-ray scattering (SAXS) has been used to study the formation of microvoids in polymers which craze or stress-whiten extensively. Specimens are subjected to a stepwise uniaxial strain, with scattering curves being obtained at each step. The increase in scattering intensity upon crazing is attributed to the formation of microvoids, and the relative size, shape, and concentration of the scattering elements are determined by a Porod analysis of the SAXS curves. The major portion of our work has been on high-impact polystyrene which shows a large increase in SAXS intensity as crazing occurs. We are able to follow the changes in void size and concentration during craze initiation and growth. Effects of temperature, molecular orientation, and matrix molecular weight have also been studied. The results add to the information on craze growth and microstructure known from electron microscopy and dilatometry. In addition, a qualitative physical model for microvoid nucleation is proposed, and the implications for toughness are discussed.
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  • 54
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 725-734 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The non-Newtonian viscosity in steady flow was measured for solutions of polystyrene (M̄w/M̄n = 1.1) in diethyl phthalate at 30.0°C. In the moderately concentrated solutions, from 6.03 × 10-2 to 5.62 × 10-1g/cm3, the viscosity data modified by frictional parameters fit the Graessley theoretical curve for a narrow distribution polymer. The dilute solutions, from 3.26 × 10-3 to 1.57 × 10-2 g/cm3, were nonentangled systems whose non-Newtonian properties could be explained by the excluded volume effect as proposed by Fixman. On the basis of the non-Newtonian data, it was concluded that the solution of 3.30 × 10-2 g/cm3 was a lower critical entanglement concentration, which was distinguished from the usual higher critical concentration for entanglement. This lower critical concentration was also found in the concentration dependence of the activation energy of flow and the absorbance at 310 nm.
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  • 55
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystal structure of p-phenylenediacrylic acid diethyl ester above the transition point was determined at 70°C by x-ray diffraction. No significant differences in molecular arrangement are found between the structures of the α2 form (above the transition point) and the α1 form (at room temperature). Since the α1 form is photopolymerized, it is concluded that selective dimerization in the α2 form results not form the crystal structure of the monomer, but from the deterioration of molecular arrangement by the formation of dimer.
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  • 56
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 803-812 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It has previously been shown that, under high stress and consequently at short times to failure, a major factor governing the environmental stress cracking (ESC) of polyethylene is the ability of a liquid environment to penetrate a growing fissure at a sufficiently high speed to maintain contact with the fracture front. In this earlier study, viscosity was shown to play a significant role in this kinetic effect. The purpose of the present paper is to demonstrate that another property of the solid-liquid system influencing ESC under these high stress conditions is the spreading coefficient of the liquid on the polymer - the parameter defining the tendency of the liquid to wet the polyethylene. It has been shown that the spreading coefficient can be considered as a force and this force in conjunction with atmospheric pressure constitutes the force necessary to drive the liquid into the growing crack.
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  • 57
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 841-850 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ozone-degradation products of polyethylenes prepared by γ-ray-Induced polymerization in ethyl alcohol, t-butyl alcohol, and 2,2,5-trimethylhexane were analyzed by gel permeation chromatography (GPC). The ozonized polymers show two discrete peaks in the GPC traces, and the ratio of molecular weights corresponding to the peaks is close to 1:2, suggesting that these polymers are composed of folded-chain crystals similar to solution-grown single crystals. The peak profiles, however, are broad and the peaks in the chromatograms shift concertedly toward lower molecular weight in the course of degradation. These findings suggest that the fold surfaces of the polymers are coarse and that there is no unique crystalline core containing a regularly folded layer. The long period estimated from small-angle x-ray measurements increases with increasing polymerization temperature, but scarcely varies with the solvent type. This implies that when crystallization occurs during polymerization, kinetic factors may have no great effect on crystallization.
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  • 58
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 907-914 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dielectric properties of vinyl acetate and methyl methacrylate oligomers having chemically different end groups were compared. Dielectric measurements were carried out over the frequency range between 23 and 3 MHz and the temperature range between +50 and -50°C. The static dielectric constants of these oligomers are between 10 and 20. The relaxations were analyzed with the Havriliak-Negami equation. The dielectric properties depend on the chain end groups on the oligomers. The distribution of relaxation times of the vinyl acetate oligomers was wider than that of poly(vinyl acetate). It was concluded that two cooperative motions, that of the principal chain and that of the chain and that of the chain end group, take part in the dielectric relaxation of these short chain molecules.
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  • 59
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 939-943 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 60
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Thermally stimulated depolarization (TSD) experiments were carried out on several polystyrene samples. They included normal head-to-tail polystyrene (atactic) obtained by anionic polymerization of styrene, amorphous and substantially crystalline isotactic polystyrene, and the newly available head-to-head polystyrene. By TSD, six maxima of current intensity occurred at specific temperatures. Their features are compared for the various samples. Only three peaks could be identified with transitions which had been found by other techniques. Peak 5, located near Tg, is the primary relaxation. Maximum 6 could be the transition found above the Tg by torsional braid analysis and called T11 for polystyrene samples. Maximum 1 seems to correspond to what is sometimes referred to as the γ transition.
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  • 61
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1009-1022 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: This study was undertaken to determine the crystal structure of poly(bis-phenyl glutarate diacetylene) (poly(BPG)). It was found that this material crystallizes in a C2/c (centrosymmetric) space group. The x-ray refinement revealed a solid solution of the monomer and polymer. It was determined that the only movement that occurs during polymerization is in the diacetylene rod (a rotation of 33°) and in adjacent phenyl groups (a rotation of 19° and a swing of 6°), while all other atomic positions in the side group remain essentially the same. An infrared investigation and the final refined atomic coordinates with their standard deviations indicates that the BPG crystal was polymerized to an extent of 35%.
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  • 62
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1041-1057 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Proton spin relaxation time measurements are reported for a series of liquid polydimethylsiloxanes covering the temperature range from -50 to 200°C. These include fractionated and whole polymer samples (Mw from 104 to 106), binary mixtures, and crosslinked material. This paper is mainly devoted to the behavior of the spin-spin relaxation (T2) which is sensitive to the low-frequency long-range configurational motions occurring in the liquid phase. These motions determine the time scale over which final motional averaging of the nuclear dipolar interactions occur, prior to the onset of normal liquid-like behavior of T2. When these motions are too slow (e.g., at low temperatures of high molecular weight) to lead to appreciable averaging of the small residual static dipolar interactions present in the liquid phase, the spin-spin relaxation exhibits pseudo-solid-like behavior. A further aspect of this work concerns the observed sensitivity of T2 to network formation which considerably restricts the long-range motions that determine T2. It is possible to determine the fraction of material present in the form of a network from the relative proportions of network and non-network T2 components. This is not only true for a permanent crosslinked network but also for a network arising from transient entanglement couplings. The dynamic nature of the latter type of a network is clearly revealed in the proton nuclear magnetic resonance measurements reported here.
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  • 63
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1115-1121 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Results of uniaxial tension and compression experiments are reported on crosslinked polydimethylsiloxane (PDMS) networks in the unswollen state over the range 0.5 〈 α-1 〈 1.2 where α is the extension ratio. Curves representing the reduced force [f] = f(V0/V)1/3(α - α-2)-1 plotted against α-1 can be approximated by straight lines for 0.5 〈 α-1 〈 0.9, in agreement with the phenomenological Mooney equation. As α-1 approaches 1, however, they tend to level off and continue into the α-1 〉 1 region with decreasing slope. These results are in agreement with the predictions of recent elasticity theories that incorporate the effect of junction-chain entanglements in the elastic free energy.
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  • 64
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1101-1113 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The viscoelastic behavior of phosphonate derivatives of phosphonylated low-density polyethylene (LDPE) was studied by dynamic mechanical techniques. The polymers investigated contained from 0.2 to 9.1 phosphonate groups per 100 carbon atoms and included the dimethyl phosphonate derivative and two derivatives for which the phosphonate ester group was an oligomer of poly(ethylene oxide) (PEO). The temperature dependences of the storage and loss moduli of the dimethyl phosphonate derivatives were qualitatively similar to those of LDPE. At low phosphonate concentrations, the α, β, and γ dispersion regions characteristic of PE were observed, while at concentrations greater than 0.5 pendent groups per 100 carbons atoms, only the β and α relaxations could be discerned. At low degrees of substitution, the temperature of the β relaxation Tβ decreased from that of PE, but above a degree of substitution of 0.1, Tβ increased. This behavior was attributed to the competing influences of steric effects which tend to decrease Tβ and dipolar interactions between the phosphonate groups which increase Tβ. For the phosphonate containing PEO, a new dispersion region designated as the β′ relaxation was observed as a low-temperature shoulder of the β relaxation. The temperature of the β′ loss was consistent with Tg(U) of the PEO oligomers as determined by differential scanning calorimetry, and it is suggested that the β′-loss process results from the relaxation of PEO domains which constitute a discrete phase within the PE matrix.
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  • 65
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1169-1179 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A craze may fracture either by the breaking of covalent bonds or by a process of “viscous rupture” involving the movement of bulk material in the craze. In the latter case it is necessary that the majority of the chain ends of the polymer molecules passing through the craze-matrix interface terminate within the craze. We have therefore calculated the probability of a polystrene macromolecule spanning a thin craze and shown that for viscous rupture a craze in a normal commercial polystyrene must be something more than 40 nm thick. As the measured craze thicknesses have generally exceeded 100 nm, a viscous fracture process is clearly possible, though, of course, chain rupture is not excluded by the argument. More difficulties arise when fracture occurs within a specified region of the craze and the possibility of a bond fracture under these circumstances is briefly discussed.
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  • 66
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1195-1217 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics of craze growth from sharp cracks in polystyrene (PS) and poly(methyl methacrylate) (PMMA) in contact with liquid methanol were measured with time-lapse photography as a function of the stress intensity factor KI. At high KI the craze length in both systems increases as √t if the sides of the craze are protected from methanol and as t if they are not, where t is the elapsed time after loading. If such a side-protected craze is dried under load and then methanol is reintroduced to the crack tip, the methanol front advances with the same kinetics as the original craze growth. This experiment Proves that solvent crazing velocities are limited by the hydrodynamic transport of solvent through the porous craze structure under a capillary pressure driving force (which can be as high as 100 atm). An improved model of fluid flow through the craze is developed and shown to predict craze growth kinetics in good agreement with those observed. The hydraulic permeability of methanol crazes in PS was found to be independent of craze length at small craze length and to be independent of KI except at very low KI. Although increases in molecular weight in the range Mw = 200,000 to Mw = 670,000 do not markedly affect the crazing kinetics, they greatly increase the time to fracture of the craze.
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  • 67
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1291-1295 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Thermoelastic measurements on a glassy polymer make it possible to measure directly the quantity αV/Cp where α is the coefficient of linear expansion, V the specific volume, and Cp the specific heat at constant pressure. By further measuring the bulk modulus (BT) it is possible to derive a relatively accurate value of the thermodynamic Gruneisen constant (γT) where γT = 3BTαV/Cv. The values obtained decrease only slightly with temperature.
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  • 68
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1325-1328 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 69
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1381-1387 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The linear thermal-expansion coefficients (α) of styrene-sodium methacrylate copolymers were studied as a function of the concentration of sodium methacrylate comonomer. Over the concentration range studied (0.61-9.0 mole % sodium methacrylate), the expansion coefficients of the glass αg and of the liquid αl were independent of ion concentration. Average values for these quantities were αg = (6.9 ± 0.9) × 10-5 deg-1 and αl = (16.0 ± 2.0) × 10-5 deg-1. When samples of concentrations above 6 mole % were heated from room temperature, a low value for the liquid-expansion coefficient αl was observed in the first runs. This quantity had an average value of (12.0 ± 1.9) × 10-5 deg-1. Heating of the 6.5 mole % sample from room temperature followed by cycling from the glass transition temperature Tg to successively higher temperatures resulted in a gradual increase in liquid-expansion coefficient. The results are consistent with the hypothesis of the existence of various types of ionic aggregates in these polymers, with the state of aggregation changing at approximately (5-6) % of ions. Experimental Tg values, which increase with ion concentration over the entire range, are consistent with the results of previous studies.
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  • 70
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1419-1434 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Small-angle x-ray scattering from solutions was applied in assessing branching using well-characterized dextran hydrolyzates. It was found that the longitudinal and cross-sectional properties of the polysaccharides vary in a manner predictable by the molecular topology of the chains. A hydrodynamically equivalent linear model for dextran is proposed and it has been shown that this model correctly predicts values of Φ and K, Flory's universal hydrodynamic constant and the Flory-Fox-Schaefgen parameter, respectively.
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  • 71
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1409-1418 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The synthesis of poly(pentamethylene terephthalate) and its subsequent drawing into highly oriented fiber has proved difficult for two reasons. First, it was difficult to produce polymers of sufficiently high molecular weight to withstand subsequent drawing; and second, because of the slow rate of crystallization of the material, the spun fiber coalesced on the windup bobbin, becoming useless for drawing. Methods are described which overcome these difficulties. Two crystalline phases of the oriented fiber have been discovered. The α form is obtained by annealing under zero or small tension and has a crystallographic repeat along the fiber axis of 24.7 Å compared with a chemical repeat of 14.5 Å. There are evidently two monomers per crystallographic repeat, each appreciably contracted. The β form is obtained by annealing either under high tension or at constant extended length, but in the relaxed fiber it always exists in mixture with the α form. Its crystallographic repeat is 28.2 Å, and so again consists of two monomers; but their conformation is more highly extended than that of the α form. An α-form fiber will transform reversibly to the β form under the influence of mechanical stress.
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  • 72
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1447-1457 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Structural relaxation in poly(vinyl acetate) (PVAc) in and slightly above the glass-transition region has been studied by monitoring the time dependence of enthalpy using differential scanning calorimetry and the frequency dependence of electric polarization by dielectric loss measurements. The results have been analyzed to yield the kinetic parameters characterizing the structural relaxation and are compared with similar analyses of previously published shear compliance and volume relaxation experiments. Relaxation of enthalpy, electric polarization, volume, and shear stress in PVAc all appear to be characterized by somewhat different relaxation times. The difference between the volume and enthalpy relaxation times, coupled with the fact that PVAc exhibits a Prigogine-Defay ratio greater than unity, is evidence for a previously proposed connection between the thermodynamics and kinetics of structural relaxation in terms of an order parameter model.
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  • 73
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1435-1446 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effects of Chemical structure on the molecular motions in linear aliphatic polyesters have been investigated with a free-oscillation torsion pendulum. Broad-line NMR provided supplementary information. In the γ relaxation which corresponds to the local-mode motions of main chains in the noncrystalline region, the polyesters which are composed of two methylene units in the diol part of the chemical repeat unit showed an extremely asymmetric loss curve with a relatively high-loss peak temperature compared with that of the other polyesters. In addition to the two relaxations (β,γ) which have been observed in earlier dielectric measurements, a new relaxation (α) was found on the high-temperature side of the glass transition of the polyesters. The α relaxation was assigned to molecular motions of methylene segments in the crystalline region. The α and β relaxations of the two-dimensional series are situated close to the temperatures found for other polyesters with rather long methylene sequence in the chemical repeat unit. The results were explained in terms of a difference on the chain mobility in the noncrystalline regions which may be related to the difference of chemical structure of the polyesters.
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  • 74
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1459-1470 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The time-dependent yielding of glassy polycarbonate subjected to constant tensile loads has been studied. Application of a constant stress of a magnitude between the yield stress and the stress required for propagation of a neck in constant strain tests results in inhomogeneous yielding after a well-defined time lag. This delay time increases with decreasing stress and temperature. The critical stress for slowly cooled material is greater than that for quenched material in which the delay time is divided in two regions. The delay time is regarded as the time required for the initiation of inhomogeneous yielding at either edge of the specimen and growth over a certain distance across the specimen. Geometrical observations revealed that the inhomogeneous yielding is shear yielding which is initiated due to stress inhomogeneities caused by mechanical imperfections at the edge of the specimen. The Eyring treatment of delayed yielding can describe fairly well the stress and temperature dependence of the delay time.
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  • 75
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1491-1498 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Pressure-volume-temperature data on melts of low-density polyethylene, polypropylene (PP), poly(butene-1) (PBT), and poly(4-methylpentene-1) (PMP) previously reported by us have been evaluated in terms of the Simha-Somcynsky hole theory of polymeric liquids by a determination of the reducing parameters P*, V*, and T* for each system. Literature data on the reducing parameters of linear polyethylene and of a branched polyethylene of intermediate density are also considered. Agreement with theory is best for the polyethylenes and deteriorates markedly in the series PBT:PP:PMP. These higher polyolefins have very low values of P*, thus suggesting a deficiency of the Simha-Somcynsky theory at high reduced pressures P̃ = P/P*. In these polyolefins, systematic variations of the reducing parameters (and molecular parameters derived therefrom) are noted and discussed. Correlations found previously between T* and the moleculer weight M0 of the effective segment of the theory or its hard-core volume M0V* are obeyed by the polyethylenes only. The higher polyolefins show serious deviations from these correlations.
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  • 76
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1471-1489 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A crystalline-state theory recently developed by Midha and Nanda is commented on and applied to the isobars of polyethylene, poly(vinylidene fluoride), and poly(chlorotrifluoroethylene) at atmospheric pressure, and to an isotherm of polyethylene. Satisfactory agreement with experiment results. This includes the volume change at the melting point Tm and the volume difference ΔV between crystal and melt below Tm, when crystal and the earlier liquid-state theory are combined. A similar agreement is noted with respect to the results at high pressure. The scaling parameters obtained indicate the approximate role of melt temperature and volume as reducing quantities. An inverse proportionality between Tm and αl, the expansivity of the melt at Tm, derived much earlier for low-molecular-weight solids, is recovered with an identical numerical coefficient. The thermodynamic functions of polyethylene are investigated in both phases. For this purpose contributions of internal harmonic modes are considered within the framework of the equivalent s-mer model. One or, at most, two average frequencies are adequate to represent the temperature dependence of the excess free energy and entropy over the value at absolute zero, when the external contributions are included for the crystal. A similar representation of the hard modes can be adopted for the melt. However, the free energy of segmental disorientation computed either from a constant entropy for the s-mer or a rotational isomeric state model for the isolated chain does not appear to be an adequate representation over a sufficient temperature range. An additional temperature-dependent term in the entropy and free energy is introduced and tentatively attributed to a volume- and temperature-dependent short-range ordering. Good agreement with experiment, including the entropy and temperature of fusion, ensues.
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  • 77
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1507-1514 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 5 Ill.
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  • 78
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1515-1518 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 79
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1499-1505 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An apparatus is described which enables the rapid recording of time-resolved emission spectra on a nanosecond time scale. The instrument permits detailed study of the time-dependent photo-physical processes occurring in many polymer systems. The technique has been used to investigate the kinetics of excimer formation in methylene chloride solutions of polystyrene and poly(1-vinyl-naphthalene). Unambiguous evidence for excimer dissociation is observed in poly(1-vinylnaphthalene) but the process appears unimportant in solutions of polystyrene.
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  • 80
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1519-1527 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new method for studying polymer network formation has been devised. Crosslinking reactions are carried out in a recording viscometer, which provides accurate determination of incipient gel points and also serves as a high-speed stirrer. The molten, nonstoichiometric mixtures are reacted to completion to eliminate the inaccuracies inherent in the determination of reaction extent and this, together with the use of esterification reactions with minimal side reactions, reduces many of the problems of previous methods. The experimental results for the reactions of simple model compounds are in very close agreement with Flory's network theory. A system containing crosslinking reagents with unequally reactive groups has also been considered and the accuracy of the method enables the reactivity ratios of the different groups to be calculated.
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  • 81
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1529-1544 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The diffusion of vapors and liquids which induce crystallization in initially amorphous, unoriented poly(ethylene terephthalate) (PET) films was studied. It was determined that these vapors and liquids penetrate the polymer as distinct fronts, and the kinetics of this penetration and the weight uptake kinetics both follow apparent Fickian behavior. Distinct cavitation advanced into the polymer at the penetrant front-dry polymer interface in certain PET-liquid systems, and phenomenological explanations of its existence and of the general diffusion process observed are offered. Finally, the diffusion of the highly interactive liquids dioxane and methylene chloride into cold-drawn PET was studied and shown to occur considerably more slowly than does the diffusion of these liquids into unoriented films.
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  • 82
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1545-1557 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The mechanical properties of initially amorphous, unoriented poly(ethylene terephthalate) (PET) films crystallized in acetone and dioxane at room temperature were studied under tensile testing conditions. It was found that the nature of the liquid, the morphology it induced, and its significant residual level trapped within the PET following this type of crystallization all influenced the observed mechanical behavior. Further, thermally treating PET at 70, 90, and 174°C prior to the liquid treatments appeared to inhibit the effects of the liquids on the resultant mechanical behavior. Finally, because these liquids penetrated the polymer as distinct fronts, laminate-type structures were generated in the films. It then was shown that an ideal parallel element laminate could adequately model the mechanical behavior of the films.
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  • 83
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1583-1592 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: There are several reports in the literature to the effect that when isotactic polystyrene crystallizes from moderately dilute solution, lamellas (precipitate) form at high crystallization temperatures and gels at low temperatures. We report here the occurrence of a very similar phenomenon during the crystallization of ethylene-butene-1 copolymers. The observations for the latter system can be given a straightforward explanation based on the demonstrated compositional fractionation that occurs on crystallization. Low co-unit content copolymers are associated with lamellas. Gels invariably contain much higher co-unit content. A generalization of these findings is invoked to explain the previous polystyrene results. A new resonance detected by 13C NMR experiments in this polymer can be ascribed to head-head sequences.
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  • 84
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1593-1609 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It is shown how the shape of the longitudinal acoustic vibration observed in the low-frequency region of the Raman spectra of crystalline polymers can be used to obtain a quantitative distribution of lengths of straight-chain segments associated with polymer lamellas. The procedure is demonstrated for a “solid-state” extrudate of polyethylene and for a bulk-crystallized specimen of the same polymer. Equations relating the shape of the LAM-1 band to the shape of the distribution curve are given. The low intensity observed for the LAM-3 mode relative to LAM-1 is explained quantitatively without recourse to end effects. LAM-5 has been observed for bulk-crystallized polyethylene. For the extrudate we find the distribution of lengths of straight-chain segments to have a tail on the long-length side which is not present for the bulk-crystallized sample. The Raman technique is shown to provide new morphological data unattainable at present by other methods.
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  • 85
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1611-1634 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The broad-line proton NMR spectra of polyethylene are separated into three components (broad, medium, and narrow) corresponding to the crystalline and two kinds of amorphous protons, respectively. All amorphous protons are found to be mobile above 210°K. The unusually low molecular mobility in the amorphous regions of polyethylene compared to purely amorphous and other partially crystalline polymers is considered to be adequately described by the network model of Edwards and De Gennes. In this model the chain motions are anisotropic and restricted to small tubular volumes. The medium and the narrow component are believed to result from two different modes of chain motion within these tubes, depending on the free volume available. Two motions in the crystalline regions are observed. One at temperatures below 110°K involves 2%-5% of the protons, depending on the crystallinity of the material, and the other beginning at 290°K involves all crystalline protons (α-process). Coupling of the amorphous and crystalline motions is found above 290°K. Several line shapes have been tested as representations of the three components. Of these the low-temperature spectrum, the Gauss-Lorentz product curve, and the Lorentz curve proved to be the most suitable shapes for the broad, medium, and narrow component, respectively. Using these line shapes, the best fit of the experimental spectra and the expected agreement of the broad and the crystalline fraction are obtained over a very broad temperature range. Above 310°K the low-temperature spectrum must be replaced by the convolution of a Gauss curve and a rectangular function to take into account the line-shape transition of the α-process. The modulation broadening of all components is considered, and this allows line-shape analysis close to the melting point.
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  • 86
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1651-1664 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: We obtain the exact solution of a fairly large class of somewhat simplified problems involving the simultaneous nonlinear Fickian diffusion of a poor solvent and a dilute organic penetrant, such as a plasticizer, in a semi-infinite polymer slab immersed in the solvent bath. Such problems can also provide useful estimates during certain time regimes of release of drugs from implants, and pesticides and pheromones from certain slow or controlled-release polymeric devices, insofar as these are affected by an environmental solvent bath. We assess the effect of various simplifications made (e.g., neglect of the penetrant concentration dependence in the diffusion coefficient, cross diffusion of solvent and penetrant, and a variety of boundary conditions) by solving exactly some additional specialized cases.
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  • 87
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1635-1649 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Small-angle x-ray scattering (SAXS) and wide-angle x-ray scattering (WAXS) as well as small-angle light-scattering (SALS) techniques have been applied to investigate the microstructure of a number of commercial poly(vinyl chloride) (PVC) samples. From the wide-angle x-ray scattering, crystallinity and crystal size parameters have been determined. The crystallinity of the samples investigated range from 5% to 10%. Superstructure parameters such as crystallite thickness, distribution functions of crystallite and amorphous thicknesses, and size of ordered regions have been obtained by an analysis of the SAXS curves using the cluster model. The crystallinity agrees well with the WAXS crystallinities indicating that most of the crystals are lamellar shaped, though some rodlike entities are present in the sample as is shown by the small-angle light scattering. From the SAXS analysis, the microstructure is described as clusters of lamella stacks which are identical with the subprimary particles. Their size is determined to be 220-240 Å. Emulsion type PVC also contains lamellar-shaped crystals. The superstructure, however, of this type of PVC is different from that of mass or suspension-polymerized material. The SAXS curve does not reveal any correlation between the crystals.
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  • 88
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1665-1670 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A method proposed for determination of high birefringence values of circular fibers is based on an analysis of the intensity of backscattered light for two orthogonal polarization directions of the incident light. The method has been used in the determination of birefringence of nylon 6-6 fiber from a circular photographic recording of scattered light. The values thus obtained are compared with those obtained by polarized light microscopy.
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  • 89
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1671-1683 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The thermodynamic treatment of crystallization phenomena in a prestretched rubber was undertaken. Emphasis was put on defining conditions for the thermodynamic stability of the extendedor folded-chain crystal structure. The extended-chain structure is found to be stable thermodynamically at temperatures higher than the isotropic melting point of un-cross-linked polymer Tm0 in the stretched state, while the folded chain one is not. Below Tm0, the stretch ratio of the network structure determines which crystal structure is more stable. The relation among the critical stretch ratio for the extended/folded crystalline structure transition, temperature, and molecular weight is also discussed. The crystallinity predicted by this work becomes zero at a temperature of Tmi, the isotropic melting point of a cross-linked system. The value of Tmi decreases with increasing cross-link density, and this is consistent with the experimental data reported in the literature.
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  • 90
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1703-1704 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
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  • 91
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1685-1701 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Porton and carbon spin-lattice relaxation times T1 and nuclear Overhauser enhancements are interpreted in terms of motions likely in linear polyisobutylene. Most of the interpretation is based on relaxation data in the literature, but some additional 1H and 13C pulse Fourier transform experiments were conducted to resolve a disagreement in the literature concerning cross relaxation between the two types of protons present in polyisobutylene. Spin relaxation in solution and the bulk is accounted for by three specific motions considered as independent sources of motional modulation of the dipole-dipole interaction. The first motion is overall isotropic rotatory diffusion which has a known dependence on molecular weight, intrinsic viscosity, and solvent viscosity for polymers in solution, and a known dependence on molecular weight and viscosity for bulk polymers. The effects of overall tumbling account for a decrease of T1 for the methylene and methyl carbons with increasing molecular weight in solution and increase of T1 of methylene carbons with molecular weight in bulk. The second motion considered is backbone rearrangements caused by the three-bond jump. This motion dominates relaxation of the methylene carbons either in solution or in the bulk allowing for the determination of the associated correlation time. The correlation time characterizing the occurrence of the three-bond jump in a 5% (wt/vol) solution in CCI4 at 45°C is 58 psec, and in the bulk at 45°C it is 11 nsec. The last motion included in the model is methyl-group rotation about the threefold symmetry axis. The methyl-group rotational correlation time is 0.20 nsec in a 5% (wt/vol) solution in CCI4 at 45°C and 0.33 nsec in the bulk at 45°C. The concentration dependence of the backbone motion contrasts strongly with the corresponding dependence of methyl-group rotation.
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  • 92
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1559-1582 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: By small-angle x-ray scattering, a systematic investigation was performed of the long spacing of poly(ethylene terephthalate) (PET) crystallized in a liquid environment. The results indicated that the measured long spacings were temperature dependent and apparently relatively insensitive to liquid type under the conditions studied. The kinetic nucleation model of polymer crystallization was found to adequately explain this dependence. The differences in the long spacings between thermal and liquid-induced crystallization were in part rationalized in terms of the suspected supercoolings involved in the respective processes. Calculation of the spherulite growth rates for liquid-induced crystallization was made on the basis of the kinetic nucleation model and the classic theory of polymer-diluent crystallization. The results were shown to agree with inferential experimental observations of these growth rates and to elucidate the physics underlying liquid-induced crystallization. Finally, use of this growth rate theory in conjunction with a previous model for overall crystallization kinetics was shown to adequately describe and predict the diffusion-limited kinetics observed experimentally for most liquid-induced crystallization situations.
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  • 93
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1705-1707 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 94
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1709-1719 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The steady-state and dynamic melt rheology for a series of poly(1-olefins) has been investigated. The series includes poly(1-butene), poly(1-hexene), poly(1-heptene), poly(1-octene), Poly(1-undecene), poly(1-tridecene), poly(1-hexadecene), and poly(1-octadecene). The flow behavior was investigated by use of a Weissenberg rheogoniometer. Measurements on poly(1-butene) were also made using an Instron capillary rheometer. The empirical relationship developed by Cox and Merz was obeyed for the entire series of poly(1-olefins) at all temperatures investigated. Graessley's theory was used to calculate the flow curves for the poly(1-olefins) from the measured molecular weight distributions. The purpose was to investigate the effect of polymer composition on the shear rate dependence of viscosity. It was found that all experimental flow curves except those for poly(1-hexene) can be fitted with the calculated curves from the individual molecular weight distributions. The conclusion is made that flow curves of poly(1-olefins) depend predominately on molecular weight distribution and are essentially independent of side-chain length even for poly(1-olefins) with pendant groups as long as 16 carbon atoms. The low-shear limiting Newtonian viscosity η0 for all poly(1-olefins) was expressed by, η0 = KM̄w3.4 or by η0 = K′P̄w3.4 where M̄w is the weight-average molecular weight and P̄w is the weight-average degree of polymerization. The K and K′ values obtained decrease systematically as the side chain is increased.
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  • 95
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1721-1728 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Solid-state extrusion of high-density polyethylene (HDPE) has received considerable attention. It has been shown that extrudate may have high values of optical clarity, tensile modulus (∼70 GPa = 7 × 1011 dyn/cm2), and c-axis orientation. The effects of extrusion conditions on the properties of the resultant fibers have, however, not yet been clarified. A systematic study has thus been made here to evaluate extrusion pressure, temperature, and extrusion (draw) ratio, and the molecular weight of extruded HDPE. The effects of extrusion ratio on the degree of crystallinity, melting behavior, crystal orientation, and dimensional change along the extrusion direction are reported.
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  • 96
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1761-1771 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dielectric absorption due to the side-group rotation of the methyl methacrylate (MMA) unit in MMA-styrene and MMA-p-chlorostyrene (pCS) copolymers was measured. The relaxation time for MMA-pCS copolymers with low MMA contents could be interpreted quantitatively in terms of the Kramers rate-constant theory at the low-friction limit. On the other hand, the frictional effect on the relaxation time could not be ignored for any copolymers except for the MMA-pCS copolymers with low MMA contents. The relaxation time for pure poly(methyl methacrylate) could be interpreted by the Kramers theory at the high-friction limit.
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  • 97
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1739-1759 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effects of pressure on the α (ca. 70°C, 1 kHz) and γ (ca. -100°C, 1 kHz) relaxations of linear polyethylene were studied dielectrically between 0 and 4 kbar. Equation of state (PVT) data were also determined in the range of interest of these relaxations. The sample was rendered dielectrically active through oxidation (0.8 C=0 per 1000 CH2). The α process (which occurs in the crystalline fraction) could be studied over a much wider temperature range than heretofore possible due to the effect of pressure in increasing the melting point. Examination of relaxation strength from 50 to 150°C showed that there must be two crystalline relaxation processes: the well-known α relaxation plus a competing one. The α relaxation is believed to be due to a chain twist-rotation-translation mechanism that results in rotation-translation of an entire chain in the crystal. The relaxation strength of the α process decreases and therefore indicates the presence of a second (faster and not directly observed) process that increases in intensity with increasing temperature. It is postulated that the second process is due to motion of defects that become more numerous through thermal injection at higher temperatures. Analysis of the relaxation data along with the PVT data allowed the constant volume activation energy for the α relaxation to be determined. It was found to be 19.4 ± 0.5 kcal/mole. The constant volume activation energy is important in modeling calculations of the crystal motions and is significantly smaller than the atmospheric constant pressure activation energy of 24.9 kcal/mole. The effect of pressure on the activation parameters and shape of the γ process was also determined. There has been controversy over whether the γ process occurs only in the amorphous fraction or in both the amorphous and crystalline phases. Since the two phases have quite different compressibilities, increasing the pressure should change the shape of the loss curves (versus frequency and temperature) if the process occurs in both phases. The shape (but not location) of the loss curves was found to be remarkably independent of pressure. This finding strengthens the view that the γ process is entirely amorphous in origin.
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  • 98
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1773-1787 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Three loss peaks in the dielectric spectra of thermally oxidized polyethylene at temperatures below 50°K are each apparently associated with specific species of nonvolatile oxidation products involving hydrogen atoms. We report how each is influenced by room-temperature rolling, heat treatment, isotopic substitution, and chemical attack. One, the Vincett-Phillips peak, is susceptible to attack by Cu2+, Fe3+, and HI, and is attributed to a hydroperoxide species. Its rapid and easy determination has promise in the study of polyethylene oxidation. Carson's (higher-frequency) peak is tentatively attributed to an alcohol species and a new (lower-frequency higher-temperature) peak is described but not yet attributed. A few additional observations are made on the loss peaks associated with antioxidants of the substituted phenol type, as reported by Thomas and King.
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  • 99
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1729-1737 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The tensile properties have been evaluated for high-density solid-state polyethylene extruded to different extrusion (draw) ratios. The results are compared with measured and theoretical values on this and other polymers. An extrusion (draw) ratio and a deformation gradient are defined and discussed. The content of extended tie molecules in extruded high-density polyethylene was calculated from a model and modulus data.
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  • 100
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    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 1789-1800 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: High-speed gel-permeation chromatography (GPC) of water-soluble polymers has been investigated by using TSK-GEL, type-PW columns packed with small porous particles. Being semirigid, the column packing could be operated under high pressure and, therefore, it was possible to achieve high-speed GPC. A resolution higher than that of ordinary GPC in organic solvent system was attained when the measurement of one sample was completed within 40 min with a 6-ft column set. Samples with a wide range of molecular weights, from oligomers to polymers having a molecular weight greater than 106, could be fractionated. Dextran, polyethylene glycol, polyacrylamide, poly(vinyl alcohol), and poly(vinyl pyrrolidone) were separated according to molecular size with no evidence of adsorption. Investigation of other water soluble polymers is now in progress.
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