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  • 1970-1974  (1,026)
  • 1971  (500)
  • 1970  (526)
  • Physics  (1,026)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 85-114 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements of the small-angle scattering power and the degree of crystallinity in melt-crystallized high-density polyethylene have been used to evaluate the “amorphous” density in situ by the relation, \documentclass{article}\pagestyle{empty}\begin{document}$ (2\pi/V)\int_0^\infty {S\tilde g} (S)dS = (\rho_{\rm c} - \rho_{\rm a})^2 \upsilon_{{\rm er}} (1 - \upsilon_{{\rm er}}) $\end{document} where V is the irradiated volume and ḡ(S) is the “slit-smeared” absolute intensity. The amorphous density is a function of sample history and is always higher than the extrapolated melt density. After slit-height correction, and within the experimental error, the ratio of the two observed long periods is 2:1 at all temperatures (25--126°C). The lamellar thickness and the average interlamellar spacing are obtained from the degree of crystallinity and the first corrected long period. At increasing temperatures between 25°C and 110°C, the lamellae become thinner while the interlamellar zone expands by almost half. Over this range the changes are reversible with temperature. Above 110°C, both the lamellae and the interlamellar region expand with temperature. The thickening is partially reversible upon recooling. Other results obtained include measurements of stacking disorder and of microstructural changes with crystallization temperature and with time at ambient temperature.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 143-160 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Work on two sheet organosilicon polymers, one derived from the mineral chrysotile and the other from the mineral apophyllite, is described. This work provides direct evidence that both these polymers are composed of sheets. In addition, it shows that in the chrysotile-derived polymer the sheets curl into scrolls, and that in the apophyllite-derived polymer the sheets are essentially flat.
    Additional Material: 14 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 209-243 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The shear creep and creep recovery behavior of narrow molecular weight distribution polystyrene samples of low molecular weight, 1.1 × 103, 3.4 × 103, and 1.57 × 104 are reported as a function of temperature, near and above the glass temperature. Time-temperature equivalence for the total creep compliance is found to be nonapplicable, and in fact the steady-state recoverable compliance, Je, is a strong function of temperature. The time-scale shift factors for the recoverable compliance are analyzed in the light of free volume theory. Viscosity data are presented for samples with molecular weights between 1.1 × 103 and 6.0 × 105. The temperature dependence of the characteristic time constant ηJe can be explained in terms of free volume concepts whereas that of viscosity η cannot. Effects of residual molecular weight heterogeneity are demonstrated.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 15-26 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The gelation reaction of acetoguanamine with formaldehyde was investigated in the light of the gelation theory for tetrafunctional amino resins described in the previous paper. The gel time and extents of reaction of formaldehyde, amino groups, and imino groups varied with the molar ratio in the feed, but values of K (the ratio of the rate constant for condensation to that for addition) and k (the ratio of the rate constant for addition of the imino group to that of the amino group) were nearly constant. When the catalyst concentration was increased, the gel time, extents of reaction of each functional group, and the values of K and k varied; in particular K increased markedly. From the results of varying the molar ratio and concentration of acidic catalyst, it was found that the number of methylol groups per molecule of acetoguanamine at the gel point was influenced by the reaction conditions but the number of methylene linkages per molecular of acetoguanamine was nearly constant at about 0.6, regardless of reaction conditions. The number-average molecular weights up to the gel point varied with the reaction conditions, but at the gel point they were all nearly constant at about 385.
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  • 5
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: New structural phenomena which can be produced in polymers at low temperatures or by the action of high forces are described and discussed. Experimental evidence supports the argument that the deformation of polymers can develop not only as a result of conformational changes of the macromolecules proper but also by transformation of more complex structural formations. The consequence of this phenomenon is the possibility of large deformations far below the glass-transition temperature in a crystalline polymer with well-developed supermolecular structure. This type of deformation takes place without molecular orientation. Another phenomenon discussed is the sharp change of supermolecular structure in crystalline polymers caused by the action of a shock wave. These effects ought to be connected with an energetic rather than entropic deformation mechanism because the transformations occur at a supermolecular level. Thus, there can be two extreme types of deformation processes: the well-known conformation changes that occur at a molecular level, and the deformation of supermolecular structures. Examples of the pure form of the latter type of mechanism obtained under extreme conditions are given.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1147-1148 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1173-1190 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polyethylene single crystals differing in lamellar thickness, both as-grown and annealed with different lamellar thickness, were irradiated by γ-rays to a dose of about 107 rad at liquid nitrogen temperature in vacuo, and then ESR measurements were made. It was found for the as-grown crystals that alkyl radicals were concentrated at the crystal surface. For the annealed crystals it was found that the radical concentration was greater than in the original crystals because of an increase in disorder with annealing. By assuming that the crystals form blocks upon annealing and that the surface and the interior of the blocks have the same trapping capacities for radicals as in the original crystals, the dependence of the size of the blocks upon variation in annealing temperature and the original lamellar thickness was estimated. This estimate is supported by the theory of the thickening process of single crystals. Two types of radical reactions with different reaction rates were found to occur simultaneously at room temperature. The rapid process was independent of lamellar thickness and was related to the reaction of radicals mainly in the surface region and the defects within the crystals. The slow process was strongly dependent on the lamellar thickness (i.e., the reaction rate was much depressed as the lamellar thickness was increased) and was inferred to be closely related to molecular motions manifested in viscoelastic measurements by the crystalline dispersion αc.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1255-1269 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: When oriented polyethylene is sheared at an angle to the orientation axis, kink bands often develop and grow, with a resulting change of the crystalline orientation. Beside the crystalline reorientation, the following changes within the kink bands have been observed with wide-angle x-rays: (a) partial transformation to a monoclinic from the normal orthorhombic unit cell; (b) partial alignment of the orthorhombic b axes; (c) rotation of the orthorhombic c axes of a fraction of the crystals around the kinks by an extra 40 to 60° beyond that of the fibrils; and (d) misalignment of the orthorhombic (hk0) planes by a few degrees. These results are suggested to arise, at least in part, from crystal flattening and from crystal twinning or pseudotwinning on planes intersecting the molecular axes.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1219-1234 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The low-frequency skeletal and intermolecular modes (below 900 cm-1) have been studied for a sample of “as-polymerized” Ziegler-Natta polyethylene for which extended-chain conformations have been proposed. These results have been compared with data from a sample of stirred-solution-crystallized polyethylene and with previous measurements for highly crystalline samples of folded-chain polyethylene. Measurements were also made of the temperature dependence of these modes for the as-polymerized material and of the polarization dependence of these modes for an oriented sample of solution-stirred polyethylene. In the neutron spectra and the corresponding derived frequency distributions, the observed major “singular” frequencies for both the skeletal and intermolecular modes are in reasonable accord with those previously observed for folded-chain samples of high crystallinity and in Raman measurements. In addition, these frequencies agree with those predicted by theory for the singular frequencies corresponding to the phase-frequency relationships for the skeletal and intermolecular modes of an infinitely extended chain in a crystal. However, in the spectra of the extended-chain materials, these singular frequencies, in general, appear sharpened and enhanced in intensity relative to those for previously reported results on folded-chain polyethylenes; consequently, assignment of their characteristic frequencies is easier. In addition, evidence is presented to show that, for the extended-chain materials, these frequencies broaden less rapidly with increasing temperature, and the corresponding average vibrational amplitudes are smaller than those observed for highly crystalline samples of folded-chain material. It is suggested that in these materials the reduction of the number of chain folds and the increased intramolecular ordering give rise to increased thermal stability of the configurations with regard to segmental rotation and to decreased vibrational amplitudes relative to folded-chain materials. When the aspolymerized materials is preheated above the normal melting point for polyethylene, the neutron spectra revert to those more characteristic of the folded-chain materials, indicating that a relaxation of chain extensions has occurred. However, on the basis of these results, on quantitative estimates of the characteristic relaxation time can be presented. Additional frequencies, besides those predicted by theory for the skeletal and intermolecular modes and those associated with either multiphonon contributions or the presence of chain folds, are observed. The origin of these frequencies remains unclear but may warrant further theoretical consideration.
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  • 10
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1344-1344 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 11
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1417-1447 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The stress-optical coefficient of poly-1,4-butadiene is measured as a function of strain, cis/trans ratio, and degree of swelling. Deviations from the Kuhn-Grün theory are found which are reduced upon swelling. Results are interpreted in terms of the Shindo-Stein theory of birefringence of polymers containing statistical segments of different sizes. This interpretation for the unswollen polymer leads to the unreasonable conclusion that the cis segment is considerably longer than the trans. Reinterpretation for the swollen polymer leads to the more reasonable conclusion that the trans segment is slightly longer than the cis. The dependence of the stress-optical coefficient on the nature of the swelling solvent is similar to the observations of Gent and Nagai and is believed to result from the effect of internal field from anisotropic solvent molecules. It is felt that the value of the stress-optical coefficient for the dry rubber is modified by the internal field from somewhat locally ordered neighboring polymer molecules.
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  • 12
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1483-1494 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The sorption and diffusion constants of CH2Cl2 at room temperature in quenched polyethylene film drawn at 60°C to different draw ratios λ between 6 and 25 drop drastically between λ = 8 and λ = 9 and then remain nearly constant, dropping only slightly up to λ = 25. Also, the exponential dependence of diffusion constant on concentration of sorbent increases abruptly in the same draw interval and then remains constant at the higher draw ratios. The data may be explained well by a composite madel: a low-permeability fiber structure embedded in a high-permeability spherulitic matrix. As the draw ratio is increased, the initially spherulitic film is gradually transformed into the fiber structure with the transformation being completed between λ = 8 and λ = 9. During subsequent drawing to λ = 25 the mutual arrangement of microfibrils, the basic elements of the fiber structure, changes by longitudinal sliding. However, their transport properties remain nearly constant. The diffusion constant drops a little as a consequence of the increased fraction of tie molecules which reduces the number of unperturbed sorption sites.
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  • 13
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1719-1724 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
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  • 14
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1729-1745 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Atactic, isotactic, and optically active poly(propylene oxides), PPOx, were irradiated with both γ-rays and electron beams. Up to a dose of 37 Mrad no change could be detected in the optical activity. G values for hydrogen evolution decreased as compared to polypropylene in about the same ratio as G(H2) of polyoxymethylene decreased as compared to polyethylene. G values for crosslinking and scission, estimated by means of gelation theories of Saito and Inokuti, were found to be greater for isotactic than for atactic PPOx. The behavior of transient infrared and ultraviolet absorption bands is discussed. Intrinsic viscosity data indicate a rapid initial chain degradation whereas CO gas and OH group production is linear with dose. Evidence for the conversion of one type of free radical to another on heating an irradiated sample from 77°K to room temperature is based on the behavior of transient infrared and ultraviolet absorption bands.
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  • 15
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1839-1850 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Steady flow and dynamic viscosities were determined for symmetrical linear and starbranched block copolymers of butadiene and styrene above their upper (polystyrene) glass transition. Block structures examined were B-S-B, (B-S-)3, S-B-S, (S-B-)3 and (S-B-)4. At constant molecular weight and total styrene content viscosities were greater for polymers terminating in styrene blocks, irrespective of branching. Branching decreased the viscosity of either polybutadiene-terminated or polystyrene-terminated block polymers, compared at equal Mw. However, comparisons at equal block lengths showed that the length of the terminal blocks, not the total molecular weight, governs the viscoelastic behavior of these polymers to a surprisingly good approximation. This unusual result is rationalized in terms of the two-phase domain structure of these polymers, which persists to a significant degree in the melt. Below the glass transition of the polystyrene blocks the effects of branching were masked by differences in the morphology of the domain structure unrelated to branching.
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  • 16
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1911-1914 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 17
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1977-1989 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystallinity of poly(β-benzyl L-aspartate) is highly variable, in a series of specimens prepared under various conditions: films cast from chloroform solutions at various evaporation rates, films cast comparatively slowly from chloroform-trifluoroacetic acid solutions, films prepared from dichloroacetic acid solution by treatment with ethyl alcohol, precipitates formed from trifluoroacetic acid solution by addition of ether. Film cast slowly from chloroform is in the highly crystalline ω form. In contrast, the conformation of the benzene rings in the ω helix obtained from the α helix by heating is distorted to some extent in comparison with the structure of the highly crystalline ω form. Crystallization and conformational changes from the α to the ω form, and from the ω to the β form upon heating, are correlated with the dispositions of the side chains, the packing of the benzene rings, and the motion of the side chains. The main chain of the α helix is distorted into the ω form when its side chains are in a favorable conformation. The α helix is stable in the disordered conformation, and it is distorted to some extent at high temperature.
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  • 18
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2111-2117 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The two types of radicals trapped in γ-irradiated poly(ethylene 2,6-naphthalene dicarboxylate) (PEN 2,6) have been identified by ESR as —O—CH—CH2—O— (radical I) and a radical located on the naphthalene ring (radical II). The relative concentrations of radicals in the gross polymer are 10-20% radical I and 80-90% radical II. Similar trapped radicals have been identified in γ-irradiated poly(ethylene terephthalate) (PET), a structurally related polymer which differs only in the aromatic moiety, but the relative radical concentrations are quite different. These results are discussed in relation to the radiation resistance of the two polymers.
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  • 19
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2253-2254 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 20
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1-13 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: General kinetic equations for the gelation reaction of tetrafunctional amino monomer with formaldehyde are formulated according to Case's gelation theory. The ratio of the rate constant of the condensation reaction to that of the addition reaction is evaluated by applying a theoretical kinetic equation to the experimental measurements. The ratio of the rate constant for addition of an imino group to that for an amino group is also determined by combining the kinetic equation, stoichiometric relation, and expression for the gel point. The total yield of resin, the yield of sol, and the number-average molecular weight of the sol fraction are discussed.
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  • 21
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 43-57 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Extinction coefficients of the characteristic infrared bands due to isomeric structural units were measured for polybutadiene and polyisoprene in CS2 or CCl4 solutions and were compared with the isomer composition determined by NMR. The NMR signal assignments were made on the basis of the spectra of deutero derivatives of the polymers. In the case of polyisoprene, linear relations were obtained between the extinction coefficients and the isomer contents determined by NMR for the absorption bands at 1385 cm-1 (characteristic of trans-1,4 units), 1376 cm-1 (cis-1,4 units), and 889 cm-1 (3,4 units). However, for the absorption bands at 840 cm-1 (characteristic of cis-1,4 and trans-1,4 units), isomerized polyisoprenes did not give such a linear relationship. In polybutadiene, the extinction coefficient for the atactic 1,2 units was found to be lower than that of the syndiotactic 1,2 unit. These experimental facts lead to the conclusion that additivity of the extinction coefficients does not always hold for diene polymers. The deviation from the linear relation may be associated with regular sequences of one isomeric conformation in the chain.
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  • 22
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 115-126 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The apparent specific volumes, φ2, of a series of poly(propylene glycol) and poly(ethyleneglycol) oligomers in aqueous solution were determined as a function of temperature from 4 to 25°C. The slope, dφ2/dT, was taken as a measure of the extent of interaction between the hydrophobic portions of the oligomer and water, higher values of dφ2/dT representing diminished hydrophobic interaction. It is suggested that the observed increase in dφ2/dT with chain length for the poly(propylene glycol) oligomers can be attributed to the previously proposed disk coiled conformation of the chain which reduces the degree of contact between the side-chain methyl groups and water as the chain length increases. This interpretation is supported by (1) the direct relationship between the difference in the thermal expansion behavior of the two oligomer series and the accessibility of the methyl groups in the poly(propylene glycol) disk-coil, and (2) the agreement between the calculated volume changes on mixing for the methyl groups and the values predicted for the disk-coil model from the Némethy and Scheraga theory.
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  • 23
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 175-179 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Equilibrium melting points in trans-1,4-polyisoprene were calculated from plots of crystallization temperature versus the experimentally measured melting points. The melting points were found to be 78 ± 1.7°C for the low-melting crystalline form and 87 ± 1.3°C for the high-melting form. Within the experimental error, melting points were independent of molecular weight above a number-average weight of 33,000.
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  • 24
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 267-281 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Oscillatory shear measurements have been made on a range of anionic polystyrene melts of molecular weights 1000--500,000. For M 〈 5000 the polymer chain is too short to act as a Gaussian coil and hence the compliance of the melt is very low. For 10,000 〈 M 〈 100,000 the compliance of the melt follows the Rouse model of the elasticity of isolated polymer molecules. It is necessary to use the Ferry, Landel and Williams extension of the Rouse theory for M 〉 40,000 to allow for the effect of entanglements on the complex modulus. For M 〉 200,000 the entangelment network dominates the compliance and the Rouse theory is no longer applicable.
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  • 25
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 283-294 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements have been made of the tensile force required to pull a disk of a model viscoelastic adhesive away from an inert rigid substrate. Over a wide range of temperature and rate of deformation of the adhesive the results were found to yield a single master relation in terms of deformation rate by means of the Williams, Landel and Ferry rate - temperature equivalence for viscous materials. Thus, the strength of adhesion is due mainly to dynamic effects in the adhesive of a viscous nature, in a similar way to the cohesive strength of viscoelastic materials. This similarity is attributed to a common failure mechanism: initial failure at a highly stressed point, followed by spreading of the failure zone under local stresses which are governed by the dynamic response of a compliant material. An increase in the strength of adhesion is observed with decreasing thickness of the adhesive layer. This is also explained by the proposed failure mechanism if failure starts at a critical amount of local deformation energy, a form of Griffith's fracture criterion.
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  • 26
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 377-381 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 27
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 437-451 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The long spacing of single-crystal mats of polyethylene was found to increase reversibly on addition of liquids which normally act as swelling agents. The magnitude of the increase follows the sequence of the solvent power which these liquid exhibit at higher temperatures. The increase in long spacing depends to a minor extent on crystallization conditions, such as concentration and crystallization temperature, but increases very markedly with the molecular weight of the polymer. Heat treatment reduces the amount of swelling, even in the range of low treatment temperatures which do not produce a foldlength increase, implying a reorganization of the fold surface. It is inferred that there is a layer along the fold surface which expands by swelling which in turn implies a disordered amorphous component. Nevertheless, such disordered material need not be an intrinsic consequence of chain folding, as its amount can be reduced to insignificant proportions, e.g., by taking molecules which are short but still fold. Thus both, the presence of amorphous disorder and the nonunique nature of such a disorder along the surface is demonstrated. Further implications for the fold-surface problem are discussed.
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  • 28
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 463-482 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Several corrections possibly required for capillary flow are based on the existence of a linear relationship between the pressure drop along the capillary and the length-to-diameter ratio at a given temperature and shear rate. Recently, the appearance of nonlinearities in this relationship has created some concern as to the cause of this behavior. The occurrence and an explanation of the nonlinearities for polystyrene form the basis of this study. A narrow-distribution, low molecular weight (20,400) polystyrene was tested in eight capillaries at temperatures of 140 and 160°C to initiate the discussion of the nonlinearity in a ΔP (pressure) versus L/D (length/diameter of capillary) plot. The sample exhibits negligible extrudate swelling at all pressures which reinforces the idea that pressure is influencing the flow. The pressure dependence of viscosity is determined using the equivalent expression of the WLF equation derived from free volume theory. Justification for its use is presented. A pressure correction, representing the increased shear stress necessary for flow of the higher viscosity material, is found to linearize the ΔP versus L/D data. A narrow-distribution, high molecular weight polystyrene (670,000) is subjected to a similar analysis at 165°C by using nine capillaries. The situation is quite different, as the high molecular weight sample is not nearly as ideal as the low molecular weight polystyrene.
    Additional Material: 14 Ill.
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  • 29
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 531-541 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dilatometric and calorimetric studies have been made of the fusion process of linear polyethylene crystallized by stirring xylene solutions at elevated temperatures. It is shown that the melting point of the crystals increases rapidly from 139.5°C to 145°C in the crystallization temperature range of 100-103°C and levels off to 146 ± 0.5°C, provided that very slow heating rates are employed. Stirrer-crystallized samples treated with fuming nitric acid show higher crystalline contents. Comparison of their enthalpies of fusion and melting points indicate that higher molecular order along the fiber axis is associated with higher crystallization temperatures. This is in general agreement with corresponding results of other modes of crystallization. The attack of fuming nitric acid on stirrer crystals is characterized by weight-loss curves similar to those of dilutesolution crystals and bulk polyethylene. The linear molecular weight dependence on time of exposure to nitric acid suggests that the oxidation proceeds mainly from the chain ends at a constant rate for samples stirred in the lower crystallization range, but an increased rate is observed for a sample stirred from xylene at 105°C. It is suggested that the lamellar overgrowths, most evident at low crystallization temperatures, are epitaxially attached to the fiber axis, whereas the smaller crossbandings observed at higher crystallization temperatures are possibly made up of elements of chains that are only partly incorporated in the highly ordered fibrous core.
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  • 30
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1763-1776 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: As in the case with other polymers previously reported, the values of the refractive index increment dn/dc of polyethylene and the n-alkanes change with molecular weight. Most of the variation may be understood by examination of the role of density in the Lorentz-Lorenz mixing equation for specific refractivity, R12 = p1R1 + P2R2 used to calculate dn/dc. It may also be shown that as the absolute refractive index difference between solute and solvent becomes smaller, dn/dc becomes more sensitive to density change of the solute.
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  • 31
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1807-1837 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Previous studies on selective degradation of polyethylene single crystals with fuming nitric acid have been extended, both by using acid of lower concentration which gave better control over the degradation, and by resorting to ozone as an oxidizing agent which among others enabled the degradation temperature to be conveniently lowered. The molecular weight distribution was followed by gel-permeation chromatography in the course of degradation. Complete consistency between these different methods has been established, modifying some of the previous conclusions reached by this method. The principal feature which emerges is that we have a distribution of fold lengths. The largest straight fold stems can stretch across nearly the entire layer defined by the low-angle x-ray period, while there is a continuous distribution of shorter folds terminating deeper down in the crystals. The limiting depth at which the number of terminating folds becomes negligible can be identified and quantitatively assessed. The method of analysis is described, and individual data are discussed in detail. This picture of a fold surface layer containing essentially adjacently reentrant folds of uneven length agrees with quite recent results on other related chain-folded systems (annealed crystals, short chains, bulk structures) obtained in these laboratories and thus appears to be of general validity. The consequences of the model for our picture on polymer crystals in particular on the nature of the “amorphous” component, are discussed.
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  • 32
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1851-1869 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A wide-line NMR study of chain segmental motion in nylon 66 has been made on a rolled sheet having “double orientation.” In this sheet the crystallite c axis, i.e., the molecular chain axis, is oriented preferentially along the roll direction, and the crystallographic (010) plane lies predominantly parallel to the roll plane, or the plane of the sheet. The direction of the applied magnetic field with respect to the sheet is characterized by two angles, the polar angle γ subtended by the roll direction and the magnetic field, and an azimuthal angle φ. NMR spectra were taken at various values of the angles γ and φ and at three temperatures -196°C, 20°C, and 180°C. The second moments of the absorption spectra taken at 180°C were compared with theoretical predictions of second moments based on two models for the high-temperature segmental motion (called the αc process) in crystalline regions of nylon 66. One model consists of rotational oscillation with amplitudes δ of segments around their axies. The second model is denoted 60° flip-flop motion and consists of rotational 60°C jumps of the segments around their axes between two equilibrium sites with the possibility that the segments also oscillate with a general amplitudes δ around each site. The experimental results are consistent with fairly large amplitudes δ, in which case both models approach the limiting case of full segment rotation. For this reason the experiments do not allow a distinction between the two models. From the second moments at -196°C and 20°C the decrease in second moment due to the low temperature segmental motion, the γ process, is obtained. This motion occurs in noncrystalline regions of nylon 66 and is found to cause a decrease in second moment which is strongly dependent on the two angles γ and φ, implying double orientation of the noncrystalline segments. It is suggested that at low temperatures the noncrystalline segments become immobilized in sites dictated by the crystallite orientation through the extensive hydrogen bonding known to exist in nylon 66.
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  • 33
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1919-1933 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new phenomenon in necking of some polymers, including poly(ethylene terephthalate) (PETP) was detected. It was found that extension of PETP films under certain conditions results in periodic stress oscillations and a periodic change in appearance of the sample. The conditions at which self-oscillations appear have been determined, and the principal regularities of this regime of deformation are described. The following factors are critical for the appearance of self-oscillation: speed of straining and compliance of the sample. The self-oscillation of stress and formation of the periodic transverse bands is attributed to heat dissipation during necking corresponding to local temperature jumps and periodic strong variation of elasticity modulus due to poor heat conductivity of the polymer. Changing the external conditions of heat transfer influences the possibility and development of the effect. The phenomenon is common for various crystallizing polymers, being dependent on physical properties of the polymer and conditions of deformation.
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  • 34
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1935-1954 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The diffusion coefficient D and solubility coefficient k of small molecules [C3H6, C4H10, (CH3)4C] are determined at very low solute concentrations in annealed linear polyethylene over a wide range of temperature above and below the melting point Tm. For measurements above Tm the specimen was lightly crosslinked by irradiation from a 60Co source. The diffusion data fit equations of the form D = D0 exp {-ΔHD/RT}. An abrupt change in ΔHD occurs at Tm: representative values (for C4H10) are 4.53 and 14.9 kcal/mole above and below Tm. At Tm, D0 also changes abruptly: representative values (for C4H10) are log D0 = -2.65 above Tm and log D0 = +2.70 below Tm. The mechanism of diffusion therefore changes at the melting point. The melt exhibits typical liquidlike characteristics (negative values of activation entropy ΔSD). The ratio ΔSD/ΔHD = 4β (β denoting the isobaric coefficient of volume expansion) holds below but not above Tm. Equations of the form k = k0 exp {-ΔHk/RT} fit the solubility data. The log k versus T-1 plots above and below Tm are parallel but separated by a step at Tm. If crystallization followed by annealing is assumed to leave a weight fraction of polymer αk (the amorphous fraction) in which the solute can absorb and if the specific solubility coefficient of the amorphous fraction is identical to that of the melt, then log αk Equals the magnitude of the step at Tm. Values of αk determined from the observed step are very close to values of amorphous fraction determined by measurement of density. The solubility experiments support the concept of polyethylene as a two-phase solid with the amorphous fraction of specific volume equal to the extrapholated specific volume of the melt. The passage of a solute molecule from one potential well to another, however, occurs by processes in the melt and the amorphous fraction which are entirely different.
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  • 35
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 407-420 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The orientation distribution function for noncrystalline structural units in polymer systems cannot be determined completely from any experimental source; only the second and/or fourth moments of the distribution function, i.e., the second and/or fourth orders of the generalized orientation factors Flmj, can be evaluated. It is there-fore necessary to estimate the distribution function from F2mj and F4mj. In this paper, a graphical representation of the state of orientation is first discussed in terms of plots of F40j against F20j for several types of distribution functions for uniaxial orientation. These are three types of extreme concentration of the distribution at particular polar angles θ0 given by θ0 = 0, 0〈θ0〈π/2, and θ0 = π/2; five types of rather realistic distributions having single maxima at θj = 0, θ0, π/2 and double maxima at θj = 0, π/2, and a single minimum at θj = θ0; and four types of more realistic distributions including Kratky's floating rod model in an affine matrix. Second, estimation of the distribution function for uniaxial orientation from F40j and F20j is discussed quantitatively in terms of the mean-square error by three approximation methods: (a) expansion of the distribution function in finite series of spherical harmonics through the fourth order, (b) approximation of the distribution function as a composite of two components, random orientation and a particular orientation distribution given by Na (cos2θj)a, Na being a constant, and (c) approximation of the distribution function by Na (cos2θj)a alone. It is concluded that when the orientation distribution is sharp, estimation by the second method of approximation gives a smaller error than the first.
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  • 36
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 483-497 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(ethyl methacrylate) and poly(methyl methacrylate) prepared by benzoyl peroxide-catalyzed polymerization were fractionated. The Fox-Flory constant K was determined for these polymers by viscometry in several good and bad solvents. Application of some empirical methods for evaluation of K are also briefly discussed in relation to our results.
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  • 37
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 517-529 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The change in the light-scattering patterns upon deforming two-dimensional disordered spherulites is shown to arise from four effects occurring upon stretching: (1) the change in shape of the spherulite, (2) the change in average orientation of the optic axes of the scattering volume elements, (3) the change in deviation of the optic axis orientation angle from its average value, and (4) the change in the distance over which this deviation is correlated. The effects of these contributions upon the experimental scattering patterns are analyzed.
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  • 38
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 585-594 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dielectric measurements on poly(vinylidene fluoride) at higher temperatures result in anomalously large values of ε′ and ε″ at lower frequencies. When a static field is applied, a drastic decrease of ε′ and ε″ occurs. The effects of a static field can be summarized as follows: (1) the field effect upon ε′and ε″ is more significant at lower frequencies; (2) with increasing field strength, the rate of decrease of ε′and ε″ with time becomes greater and the ultimate values are smaller; (3) when the field is removed, ε′and ε″ recover but the ultimate recovery is incomplete; (4) the field effect depends strongly on temperature. Such behavior seems to be attributable to the displacement of ionic impurities and to their electrolysis. These results provided a method to remove the contribution of ionic impurities to ε′and ε″ and to measure the relaxation process due only to dipoles of a polymer. The application of this method revealed the dielectric high temperature absorption which had been masked by the ionic conduction in poly(vinyl fluoride).
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  • 39
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 615-632 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A polymerization mechanism in which monomers and dimers add to a growing polymer chain with different rate constants and different stereospecificity is considered. A fraction of the dimers are in isotactic placement internally, and low conversion to polymer is assumed. The stereosequence distribution generated by this monomer-dimer model is calculated and found to be non-Markovian in general. A method of determining kinetic parameters of the mechanism from experimentally obtained placement sequence probabilities and related experimental tests for the applicability of the mechanism are also described. A few ramifications of the general monomer-dimer model are then discussed. A case of special interest is the one in which all the dimers have a single internal tacticity, a model recently proposed by Blumstein, et al., for a polymerization involving the surface of certain aluminosilicate minerals. For the case where all dimers are isotactic, it is found that although the propagation of consecutive syndiotactic placements alone is simple Markovian, the overall stereosequence distribution is non-Markovian. Another special case of interest is the limiting case with dimers only in the feed. This case turns out to correspond to a special case of the cyclopolymerization mechanism proposed previously by Reinmöller and Fox. Although the tacticity distribution of the placements created by the head (or tail) monomer units alone of the dimers is Bernoullian, the composite stereosequence distribution is again non-Markovian.
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  • 40
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 669-686 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dynamic mechanical and dielectric properties of various kinds of polystyrene, including bulk-polymerized, monodisperse, isotactic, and thermally degraded samples, have been measured below the glass temperature to 4°K. Five relaxation processes are found, designated β, γ, γ′, δ, and ε in order of descending temperature. The β peak (350°K at 10 kHz) is attributed to the local oscillation mode of backbone chains and the γ′ peak (180°K at 10 kHz) to rotation of phenyl groups. The δ peak (100°K at 10 kHz) is observed only in dielectric properties of the bulk-polymerized sample and is assigned to weak polar bonds, such as oxygen bonds in the chain. The δ peak (55°K at 10 kHz) which is prominent in dynamic mechanical properties is interpreted in terms of lattice defects due to a syndiotactic diad inserted between isotactic sequences in a chain or vice versa. The ε peak (ca. 25°K at 10 kHz) is first reported in the present work, but the mechanism involved is not yet clear.
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  • 41
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 731-745 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: General expressions for determining the pressure coefficient and axial distribution of the viscosity and pressure in capillary flow are derived for Newtonian and shear-thinning fluids. The pressure-dependent viscosity model is obtained from the WLF equation as derived from Doolittle's free volume theory. The model has also been derived from Eyring's hole theory for viscosity. Poiseuille's equation is modified to correct for the pressure effect on viscosity. A Newtonian, low-molecular-weight polystyrene and a shear-thinning, high-molecular-weight polystyrene were tested in an Instron capillary rheometer. The axial velocity distribution was found to be negligibly affected by pressure whereas the viscosity was shown to increase markedly with a decrease in volume. The resulting pressure effects on the viscosity of both samples were analyzed by using the derived expressions.
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  • 42
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics of aminolysis of 1,2;3,4-meso-erythritol dicarbonate and 1,2;3,4;5,6-mannitol, sorbitol, and dulcitol tricarbonates by n-butylamine in dimethylformamide solution was investigated. The dicarbonate and tricarbonates are considered respectively as models of dyads and triads in the poly(vinylene carbonate) chain. The theoretical kinetic curves for the dimer and the trimers were calculated by solution of kinetic equations and close agreement with experiment was obtained. A version of the Monte-Carlo method was developed to provide a model for the reaction process by a computer calculation including the neighboring group effect in enhancing reactivity. The theoretical curve for a trimer coincides with the experimental one. These results confirm the accelerating influence of the unreacted neighboring groups. For the polymeric chain the experimental and calculated curves deviate for conversions beyond 10%. This indicates an additional polymer effect, which is as yet unexplained.
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  • 43
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 815-827 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystallization of a series of “odd-odd” polyamides has been examined for a variety of fusion conditions and crystallization temperatures. Diverse kinds of spherulites and other crystalline structures have been formed in these nylon polymers by direct crystallization from the melt and by melt-seeding techniques. The structures formed in this way have been characterized primarily with the aid of optical microscopy. In this series of polymers, characteristic textural features yield a fairly unified pattern of crystallization behavior. Crystalline aggregates are formed near the respective melting points of these polymers. In very thin sections (ca. 0.1μ), plateletlike crystals of high crystallinity exhibit optical and diffraction behavior characteristic of single crystals.
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  • 44
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 917-926 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dielectric properties of calcium chondroitin-4-sulfate were studied as a function of frequency, temperature, and water content. The dielectric constant changes very little with water content below “monolayer” coverage, and after that the dielectric constant follows the shape of the adsorption isotherm. The dielectric behavior is discussed as affected by interfacial polarization and by the increase in the rotational freedom of the polymer side chains.
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  • 45
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 895-915 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Extremely thin polypropylene films formed by evaporation of dilute solutions floating on water, thin films deposited on Mylar or on carbon-coated Mylar, and bulk samples were deformed; after etching with aqua regia or chromic acid, the surfaces were studied by electron microscopy of surface replicas. At small draw ratio, microfibrils with lateral dimensions of about 200 Å, originating in micronecks at crack boundaries of the original crystal lamellae, were obtained in isolated areas exhibiting maximum local strain separated by large regions of much less deformed material. With increasing draw ratio the necked regions grow, the old structure gradually being reduced to smaller and smaller islands until it disappears completely. The inhomogeneity of strain in adjacent bundles of microfibrils creates a great many longitudinal voids with more or less disoriented microfibrils bridging the gaps. The regular arrangement of crystalline blocks of rather uniform length and width can be occasionally seen on surface replicas of drawn samples, and much better on dark-field electron micrographs of drawn and annealed thin membranes. In the latter case the blocks are very uniform and have similar dimensions along and perpendicular to the axis of the microfibril. The evidence from the electron micrographs, together with previous small-angle x-ray scattering data, supports Peterlin's molecular model for plastic deformation of crystalline polymers.
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  • 46
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1083-1096 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Drawn and subsequently annealed polyethylene film was restretched along the original draw axis at various temperatures. The internal deformation was analyzed in terms of the structural parameters of a simplified model. The elementary deformations are the rotation of crystals around the b axis and shear at the crystal interface. The rigidity of the crystal plays an important role during extension; and as a result, disorientation of chains in the crystal occurs at high strain. At the same time, crystals deform in such a way that the crystalline chains tilt about the b axis along the (h00) plane. This deformation of the crystal is affected by temperature. The increase in long spacing with extension can be interpreted roughly by the changes in structural parameters. The strain in amorphous region in also discussed in relation to these parameters.
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  • 47
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1133-1145 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The glass transition temperatures of a number of poly(vinyl phenyl ketones), poly-(vinyl benzoates), and poly(phenyl acrylates) have been measured by a refractometric method. The effects exerted on Tg by the nature and position of the ring substituents and by the different groups binding the pendant phenyl rings to the polyvinyl chain are discussed. The importance of knowledge of the side-group motions in the glassy state for the interpretation of glass temperature data is emphasized.
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  • 48
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1153-1171 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The relation between molecular weight, chain rigidity and the length of the high-elasticity plateau is determined from frequency and temperature dependences of the storage modulus for polybutadienes and polystyrenes with Mw/Mn ≤ 1.1. Use is made of the concept of equivalence of high-elastic states characterized by equal lengths of high-elastic plateaus for linear polymers. The high-elastic states of the linear polymers studied are equivalent if the polymer chains have equal numbers of dynamic segments and if the reference temperature is T0 = 1.22Tg, where Tg is the glass transition temperature. The viscoelastic properties of the polymers in the high-elastic state are determined unambiguously by Tg and the molecular weight of the dynamic segment. The quantitative relation between thermomechanical characteristics obtained by measuring deformation versus temperature under a constant time regime and dependence of storage modulus versus frequency under isothermal conditions is discussed.
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  • 49
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1243-1254 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The size and distortion of crystallites in samples of linear polyethylene were determined before and after plastic deformation. A slowly cooled sample, a quenched sample, and highly drawn films (draw ratio 16) were investigated by different methods. Wide-angle x-ray patterns were analyzed to study the average size of the crystalline mosaic blocks and their distortion. In addition, the longitudinal crystal thickness (in the chain direction) was evaluated by two other approaches, determination of the long period, and the melting temperature of irradiated samples. The results show clearly that the size of the crystalline mosaic blocks changes substantially with drawing of polyethylene. Not only is the lateral crystal thickness affected, but the longitudinal crystal dimensions also change during the drawing process. By the three independent methods we find that the longitudinal crystal thickness after drawing is independent of the value for the undrawn samples, as was reported earlier by Peterlin. The change in crystallite size after drawing is accompanied by a large decrease in crystal volume to about 10% of the value for the undrawn sample. The degree of distortion in the crystals seems not to be affected by the deformation process. These experimental data can be considered evidence for high chain mobility and for the possibility of rearrangement of chain molecules during the process of plastic deformation.
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  • 50
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1305-1324 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It has been demonstrated that the fold surfaces of polymers can be specific towards chemical attack, if the reaction is mild and nondestructive of the fold. Bromination of suspensions of single crystals of polyethylene in carbon tetrachloride has been shown to be such a system. This chemical modification of a fold surface is a powerful means of extending the applications of the physical methods available. Several methods were used, among them DTA, DSC, infrared spectroscopy and small-angle x-ray diffraction. Experimental results from these methods lead to the following conclusions. (a) Bromination takes place preferentially at the folds and is consistent with a regular adjacent reentry fold model. (b) Annealing of these brominated crystals demonstrates the major role played by the crystal surface in this process. (c) The preparation and properties of a novel copolymer system has been demonstrated. It is felt that this copolymer system may prove a useful addition to those systems presently available.
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  • 51
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 52
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1379-1397 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The sedimentation-equilibrium method is extended to treat nonideal solutions of heterogeneous macromolecules. The solute is assumed to be heterogeneous not only in molecular weight but also in other quantities such as partial specific volume, second virial coefficient and specific refractive increment. General expressions for various observable molecular weights, especially for weight-average, z-average, and number-average molecular weights, are derived. Their dependences on sedimentation parameter and solute concentration are discussed in detail. For the extrapolation of observable molecular weights, giving a type of weight-average, and z-average, to infinite dilution to estimate the molecular weight and the second virial coefficient, average concentration is superior as a concentration variable to original concentration. The plots of observable molecular weight versus average concentration are usually less influenced by the choice of the sedimentation parameter, especially of rotor speed. The general expressions are applied to a few special cases; monodisperse polymer, polydisperse homologous polymer, and polymer blend. The results are compared with experiments on a monodisperse, polystyrene, a polydisperse poly(methyl methacrylate), and a mixture of the two polymers, all in 2-butanone at 25°C. The agreement between the theory and experiments is satisfactory.
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  • 53
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1471-1481 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Single crystals of amylose V complexes with the 81 helical configuration can be obtained from aqueous solutions of amylose by using α-naphthol as a complexing agent. Morphological observations suggest that the differences in crystallization behavior among the α-naphthol complex and other complexes with alcohols are due to differences in solubility of the complexes in water. Electron diffraction studies indicate a two-dimensional tetragonal unit cell with a = b = 22.9 Å. It is deduced that the space group providing a satisfactory arrangement of two helices is one of the enantiomorphs P41212 and P43212. From x-ray diffraction it was found that the c axis spacing of the α-naphthol complex is equivalent to that in 61 and 71 helical amylose crystals. Consequently, the geometry of the helical configuration requires an integral number of glucose residues per turn. The true helical diameters of the n-butanol, isopropanol, and α-naphthol complexes were calculated from experimental data. The ratio was 6:7:8 and indicated that the helix of the α-naphthol complex has eight glucose residues per turn. The diversity of helical configurations in V amylose crystals is discussed.
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  • 54
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1517-1523 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A vibrational analysis has been carried out for the two crystalline forms of poly(vinylidene fluoride) (PVF2). The Raman spectrum of the planar form of PVF2 is also reported. The band assignments are made on the basis of the spectral properties including the infrared dichroism and Raman intensities. A force field is derived based on a force constant refinement procedure utilizing the frequency data for both crystal forms.
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  • 55
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1537-1551 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An attempt is made to analyze the relationship between salt rejection and water flux of nonionic polymer membranes in reverse osmosis on the basis of the movement of water in the membranes. The salt rejection Rs is a consequence of transport depletion of salt in relation to water flux. The transport depletion can be quantitatively expressed through knowledge of the mode of water transport and by application of free-volume theory to membrane transport phenomena. Water permeation can be characterized by a parameter ω = RTK1/P1v1, K1 denoting hydraulic permeability, P1 diffusive water permeability, v1 the molar volume of water. Thus polymer membranes can be classified in three categories: ω = 1 (diffusion membranes); ω 〉 1 (diffusion-flow membranes); and ω ≫ 1 (flow membranes). Salt rejection Rs can be expressed in terms of P1, the diffusive salt permeability P2, and the effective pressure (Δp - Δπ): \documentclass{article}\pagestyle{empty}\begin{document}$ R_{\rm S} = \{ {\rm \omega } + [P_2 RT/P_1 v_1 (p - {\rm \pi )]\} }^{{\rm - 1}} $\end{document} Experimental results obtained with various hydrophilic polymers are presented as the dependence of Rs on the logarithm of water flux. Good agreement was found between the experimental data and the calculated curve. Excessive swelling of membranes results in bulk flow of water (high ω) with coupled transport of salt. Hence the salt rejection decreases quickly as water flux in creases beyond a threshold value above which water flux can be characterized as bulk flow.
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  • 56
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1603-1627 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Transition and relaxation phenomena in 26 structurally related polyquinoxalines and other aromatic polymers were studied over a temperature range from 70 to 770°K by means of calorimetric, dilatometric, dynamic mechanical, and dielectric techniques. Differential thermal analysis and x-ray data showed these polymers to be essentially amorphous. The lack of crystallinity is attributed to geometric isomerism, resulting in conformational as well as configurational disorder. Calorimetric measurements gave discontinuities in heat capacities ranging from 12 to 54 cal/°C per mole of repeat-unit structures and provided unambiguous assignments of glass transition temperatures of these polymers. Depending upon structure, Tg varied from 489 to 668°K. Thermal expansion curves of annealed bulk polymer samples between 70 and 770°K exhibited only one discontinuity over the entire temperature range, namely at Tg, thus indicating the absence of any motion leading to transitions in the solid state of these polymers. Viscoelastic properties were obtained by means of torsional braid analysis and a longitudinal vibrational apparatus. In a typical case, the dynamic mechanical relaxation spectrum contained three loss maxima. A peak of low amplitude occurring at 483°K was attributed to impurity effects, resulting from endgroups and species of low molecular weight. The second and only major relaxation process occurred at 579°K, in the glass transition interval. A third, weak loss peak of unknown origin was found in the liquid state at 683°K. On the other hand, the dielectric loss curves of various polymers exhibited only one broad and strong absorption maximum at temperatures 30 to 100°K higher (depending upon a particular polymer) than equivalent major mechanical loss peaks. These differences are interpreted from a mechanistic point of view. Major mechanical relaxations occurring in the glass transition interval of these polymers are proposed to result from translational motions.
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  • 57
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1669-1679 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The fluorescence quenching of the doubly charged quinine cation by Fe++, Ag+, and Br- was studied in the presence and absence of polyvinylsulfonate (PVS). The quenching by cationic species was greatly enhanced by PVS at low polyion concentrations; at higher concentrations of PVS, the fluorescence intensity increased owing to displacement of the quinine cations from the polyion domain. Quenching of quinine fluorescence by Br- was repressed by PVS. Interpretation of the data with the use of Fe++ as the quenching agent led to “effective concentrations” of counterions in the polyion domain similar to those calculated from the catalysis of the redox reaction of Co(NH3)5Cl++ with Fe++. This may indicate that the reagent ions are not rigidly bound to the polyion chain, since such binding would affect differently processes with high and low activation energies. The Stern-Volmer constant for self-quenching of the quinine fluorescence can also be obtained from fluorescence intensity data in PVS solution.
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  • 58
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1703-1717 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The viscoelastic properties of a 4% solution of monodisperse polystyrene (molecular weight 394,000) in Aroclor 1260 were determined by the following techniques: creep recovery, stress relaxation upon cessation of steady flow, dynamic measurements, and normal stress difference and shear stress measurements in steady flow. All measurements were carried out with cone and plate geometry in a Weissenberg rheogoniometer. The modification of this instrument to perform creep and creep recovery experiments by use of an air-bearing suspension and an air-turbine drive is described. A broad range of shear rates and frequencies encompassing both linear and nonlinear behavior was employed. The elastic behavior is described in terms of the recoverable shear strain s or the steady-state compliance Je°. The first three techniques gave identical results for Je° in the range of linear viscoelasticity for which it is defined. The normal stress difference measurements confirmed Lodge's relation s = (P11 - P22)/2σ21. Reasons for previous experimental disagreement with this result are discussed.
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  • 59
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1747-1761 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The contribution to the disorder scattering by imperfect spherulites resulting from fluctuations in the magnitude of the anisotropy is analyzed for two-dimensional spherulites. The fluctuations are described in terms of a parameter characterizing the meansquare amplitude of the fluctuation and a correlation function describing the distance over which the correlation occurs. Cases considered are those where the correlation depends on either the radial or the angular separation of the scattering volume elements. As with the case of disorder in orientation, one finds that disorder in anisotropy may result in a nonzero value of intensity at μ = 0° and 90°, a decrease in the higher-order variation of scattered intensity with θ, and an increase in the intensity of scattering at higher values of θ over that for a perfect spherulite. In addition, disorder in the angular direction leads to an increase in the scattered intensity at small values of θ as compared with the zero intensity of scattering from a perfect spherulite at θ = 0°.
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  • 60
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1777-1791 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ozone has been used as a selective oxidizing agent for degrading polyethylene single crystals at room temperature in order to confirm and extend results on surface structure obtained by use of fuming nitric acid at temperatures above 60°C. The surfaces of the crystals were rendered highly accessible to the ozone gas by preparing the crystalline material in a highly expanded form; the solvent in which the crystals were suspended was removed by sublimation from the solid state. The extent and nature of the reaction were studied by measuring the increase in weight and in density, by direct chemical analyses, and by making use of infrared spectroscopy and gel-permeation chromatography. It was found that the surfaces of the crystals are attacked at room temperature by ozone, with resulting chain scission, and the broad features of the chemical reaction were established. Some folded chains are found to be as long as the original thickness of the crystal, and once folds have been cut, continuing reaction shortens the chains. In the early stages of the degradation, during which most of the weight increase takes place, the density of the crystals increases, and the magnitude of the increase is that expected from the increase in weight alone, i.e., assuming no increase in effective volume.
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  • 61
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1907-1910 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 62
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1955-1976 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effects of mean residence time, initiation rate, and emulsifier concentration on particle formation, particle growth, and polymerization rate are examined for the emulsion polymerization of styrene in a completely mixed continuous stirred-tank reactor. Experimental measurements of number of particles, particle size distribution, polymerization rate, and molecular weights are compared with theoretical predictions. A theoretical model which incorporates Stockmayer's modification of the Smith-Ewart theory into the particle growth equation allows reasonably accurate prediction of polymerization rate, particle formation rate, and particle size distribution. Agreement between experimental measurements of number-average and weight-average molecular weights and a theory based on Smith-Ewart case 2 kinetics is also reasonable.
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  • 63
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2009-2021 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The storage (G′) and loss (G″) shear moduli have been measured in the frequency range from 0.04 to 630 Hz for solutions of narrow distribution polystyrenes with molecular weights (M) 19,800 to 860,000, and a few of poly(vinyl acetate), M = 240,000. The concentration (c) range was 0.014-0.40 g/ml and the viscosities of the solvents (diethyl phthalate and chlorinated diphenyls) ranged from 0.12 to 70 poise. Data at different temperatures (0-40°C) were combined by the method of reduced variables. Two types of behavior departing from the usual frequency dependence describable by the Rouse-Zimm-Tschoegl theories were observed. First, for M ≅ 20,000, the ratio (G″ - ωηs)/G′ in the neighborhood of ωτ1 = 1 was abnormally large and the steady-state compliance Je0 was abnormally small, especially at the lowest concentrations studied. Here ω is circular frequency, ηs solvent viscosity, and τ1 terminal relaxation time. Related anomalies have been observed by others in undiluted polymers at still lower molecular weights. Second, at the highest concentrations and molecular weights, a “crossover” region of the logarithmic frequency scale appeared in which G″ - ωηs 〈 G′. The width of this region is a linear function of log c; the frequency dependence under these conditions can be represented by a sequence of Rouse relaxation times grafted on to a sequence of Zimm relaxation times. For each molecular weight, the terminal relaxation time τ1 was approximately a single function of c for different solvents of widely different ηs. At lower concentrations, τ1 was close to the Rouse prediction of 6ηM/π2cRT, where η is the steady-flow viscosity; but at higher concentrations, τ1 was proportional to η/c2 and corresponded, according to a recent theory of Graessley, to an average molecular weight of 20,000 between entanglement coupling points in the undiluted polymer.
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  • 64
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2081-2093 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Terephthalamide nylons with two to five carbon atoms in the aliphatic portion of the chain have been crystallized from aqueous solutions of hexafluoro-2,2-propandiol. The 3T and 4T nylons in particular form rodlike crystals. Indications are that these are bundles of cylindrical structures about 50 nm in diameter. Electron diffraction shows the symmetry to be C2v. Films of the nylons were drawn with great difficulty. The x-ray diffraction on the films is consistent with a monoclinic structure, though the crystal structure could not be positively established. There is some evidence for a polymer chain alignment perpendicular to the long axis of the rods.
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  • 65
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2043-2060 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In order to elucidate the relations between morphological habits and chemical structure of polymers, poly(ethylene sebacate), poly(hexamethylene sebacate) and poly(decamethylene 1,16-hexadecanedicarboxylate) were crystallized from dilute solutions in n-hexanol, isoamyl acetate etc., and were studied with the electron microscopy and x-ray diffraction. The crystal structure of these polyesters are tentatively determined. Morphological “regularity” and “simplicity” of the single crystals are correlated with the chemical structure of the polymers. The crystallization conditions under which “regular” and “simple” single crystals are obtained are relaxed with increase of methylene sequence length in chemical repeat unit. The Bragg extinction bands in the single crystals of poly(hexamethylene sebacate) and poly(decamethylene 1,16-hexadecanedicarboxylate) suggest nonplanar nature of these crystals. The molecular chains in the poly(ethylene sebacate) single crystals are inclined from the normal of the basal plane; the fold surface corresponds to the (001) plane.
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  • 66
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2105-2108 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 67
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2131-2135 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It is shown that the glass transition temperatures of the ionic acrylates are subject to the same correlation as found for the phosphates, silicates, and ionenes; the equation is Tg = 730 (q/a) - 67, where q is the cation charge and a the separation between centers of charge for the cation and anion.
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  • 68
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2151-2163 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An apparatus has been constructed for following changes in the dichroism of a polymer film undergoing rapid elongation. By means of a rapidly rotating mirror with evenly spaced open sectors, a beam of radiation is passed through the sample and then alternately polarized in the horizontal and vertical direction so that the horizontal and vertical absorbances may be rapidly compared in time as compared with the time of sample elongation (a few milliseconds). The apparatus utilizes reflection optics and a grating monochromator so that measurements may be made by using ultraviolet, visible, or infrared radiation. The transmitted intensity is detected by a photomultiplier or semiconductor infrared device, the output of which is amplified and displayed on an oscilloscope. A temperature-controlled sample chamber is provided. The operation of the apparatus is illustrated by following the change in dichroism of a sample of dehydrohalogenated poly(vinyl chloride) with visible radiation during rapid extension.
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  • 69
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The small-angle light scattering (SALS) theory for optically anisotropic spheres and disks is examined in depth. An error is found in the existing sphere equations. The correct form of the equations is identified and then experimentally verified for dilute starch suspensions. Increased concentrations and solid films of starch granules are used to identify the effect of concentration on the scattering envelope. Spherulitic films of isotactic polypropylene, isotactic polystyrene, nylon 610, PET, and nylon 66 are then used to examine different aspects of the SALS theory. Experimental observations are found to agree with the predictions of the correct SALS equations. Disk theory is interrogated and correlated with predictions for spheres. It is found that the predicted patterns from spheres and disks are very similar under identical optical conditions, in contradiction to earlier predictions. A method is developed for identifying the optical sign of spherulites too small to be seen in the optical microscope. This study constitutes a comprehensive examination of SALS theory and includes many other aspects of the phenomena. A catalogue of theoretical Vv SALS patterns from spheres and disks is also included.
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  • 70
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 295-311 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A theoretical calculation of the Hv light-scattering patterns for deformed three-dimensional spherulites is presented. Affine deformation is assumed. The optic axis of the scattering element is allowed to lie at an arbitrary angle ß to the radius which is permitted to change in the course of the deformation in a manner that may depend upon the angular location in the spherulite. The consequences of twisting of the optic axis about the spherulite radius are also explored.
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  • 71
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 331-343 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The adsorption of polydimethylsiloxane polymers from solution on glass has been studied. The amount of polymer adsorbed depends markedly on the solvent because of specific solvent - surface interactions. The presence of silanol groups in the polymer, particularly as endgroups, markedly increases the amount of polymer adsorbed. Large differences are shown between the adsorption of the commercially available, and fully trimethylsilylated polydimethylsiloxanes of narrow molecular weight distribut on. Possible adsorption mechanisms are discussed.
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  • 72
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 383-384 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 73
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 421-430 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A method is given for the analysis of long-chain branching in polymers by using combined GPC and intrinsic viscosity measurements. A computer program was written to evaluate branching indices by a tabular, iterative method. The method was applied to the evaluation of long-chain branching in low-density polyethylene.
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  • 74
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 431-435 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effects of stereoregularity on the low-temperature relaxation processes were studied by dynamic mechanical measurements on isotactic and syndiotactic polyisobutyl methacrylates (iso-PiBMA and syn-PiBMA). The α, β, and γ relaxation processes were observed in both stereoregular forms. Both the α, and β loss peaks were at lower temperatures for iso-PiBMA than for syn-PiBMA. The γ loss peak was observed at about -155°C at 30 Hz for both forms, and the apparent activation energy of this process was same for both samples within experimental error (6.7 ± 0.5 kcal/mole). It was reduced from these results that the α and β processes are both considerably influenced by the isotactic configuration but the γ process is not.
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  • 75
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 543-555 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Photocurrents developed in polyethylene in the wavelength range 360-180 nm have been measured. The action spectra show features which can be related to the corresponding features in the absorption spectrum, and in addition there is electron injection from the metal electrode at a wavelength determined by the electrode material. The time dependence of the response indicates that a long-lived space charge is formed in the material.
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  • 76
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 569-576 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Large photocurrents have been observed in films of some simple polymers (containing no π-orbitals), of which poly(vinyl fluoride) is a typical example. Not only are the currents large (up to 10-5 A/cm2) but also they are capable of being excited by light in the visible wavelength region where absorption by the polymer is too low to be detectable. The results indicate that the effects are electronic, rather than ionic, in nature.
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  • 77
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 577-584 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It was previously shown that for a stationary random copolymer of A, B, and C, we have in general p(AB) + p(AC) = p(BA) + p(CA), etc., in place of p(AB) = p(BA) which is valid for a stationary binary copolymer. Here, p(AB) for example, is the probability that a randomly picked pair of consecutive comonomers in the polymer consists of an A followed by a B. For a stationary ternary copolymer produced by a first-order Markovian addition mechanism, we show that PABPBCPCA/PACPCBPBA = k, where k is a constant characteristic of a particular set of three monomers but independent of its composition. Here, PAB is the conditional probability of finding a monomer of B given that its immediate predecessor is an A. We further show that if the individual rate constants of the monomer additions involved take a special form such as used in the Alfrey-Price Q-e scheme, then we have k = 1 irrespective of the kinds of monomers, and in addition we have p(AB) = p(BA), p(AC) = p(CA), etc. Thus, although these latter results were previously proposed by Ham as an alternative basis to supplant the Q-e scheme, they may rather be regarded as mathematical consequences of special assumptions adopted for the form of the individual rate constants. For a stationary random copolymer of four components A, B, C, and D, we have p(AB) + p(AC) + p(AD) = p(BA) + p(CA) + p(DA), etc., in general. For a first-order Markovian four-component copolymer, we show that there are seven different combinations of the conditional probabilities that are constants (k1, k2,…, k1) independent of the monomer composition. Again, if we assume the same special form for the rate constants involved, we find that all the seven constants k1, k2, …, k7 reduce to unity and p(XY) = p(YX) for X,Y, = A, B, C, D.
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  • 78
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 717-729 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Several copolymers as well as homopolymers of vinylidene chloride and vinyl chloride have been examined by Raman spectroscopy. Probabilities of concentrations of monomer sequences have been calculated from known reactivity ratios. Surface scattering intensities at some frequencies were found to be linearly proportional to specific microstructure concentrations. Normalization of scattering intensities was accomplished using the intensity of the CH2 asymmetric stretching mode at 2926 cm-1, which is common to all samples examined. Good correlation was found for the concentrations of comonomer sequences {B}, {BB}, {BBB}, {AA} and {AAAA} in which A denotes vinylidene chloride and B vinyl chloride.
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  • 79
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 755-758 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The mass flux entering the Fick's diffusion equation is considered as an arbitrary analytical function of concentration, concentration gradient, and of the gradient of concentration gradient. The restrictions imposed on the flux by the principle of material objectivity are stated and briefly discussed.
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  • 80
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 759-762 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 81
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 801-814 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of temperature and strain rate on the compressive yield behavior of polystyrene is compared with the effect of the same variables on crazing in tension. The results support the conclusion of other, more extensive work, which shows that crazing involves the same types of molecular processes as those which occur during deformation under compression and shear. An improved method of measuring compressive stress-strain curves is then described, and the compressive yield stress is also compared with an extrapolated tensile yield stress. The difference between the two is in line with concepts which assume a dependence of yield stress on the state of hydrostatic tension (or compression). It can be adequately described by the Mohr-Coulomb yield criterion. Application of this criterion also enables a theoretical stress strain curve in tension to be derived from other results in compression. Comparison of the tensile stress-strain curve so obtained with those which can be directly measured with other plastics, supports the hypothesis that crazing is favored by a marked decline in engineering stress during tensile elongation (plastic instability).
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  • 82
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 887-893 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: To determine whether the large differences in adhesion for polyethylene coatings applied to different types of copper surface could be attributed to changes in work of adhesion or wettability, the variations of contact angle with time has been measured for molten polyethylene droplets on these surfaces. It is concluded from these measurements that the low peel strengths obtained on certain substrates cannot be accounted for by a low work of adhesion of poor wetting of the surface.
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  • 83
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 927-937 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Stress-optical coefficients have been determined for crosslinked samples of polyethylen (PE) and polystyrene (PS) at high temperatures, i.e., in the rubberlike state, and when swollen in a variety of liquids. For PE, swelling liquids with long straight molecules gave large values of optical anisotropy whereas liquids with more symmetrical molecules gave minimum values, as found previously for cis- polyisoprene and trans-polyisoprene. This solvent effect is attributed to short-range orientational order in molecularly asymmetric media. Sizes of the equivalent random link for unperturbed molecules of these three polymers were deduced from the minimum values of optical anisotropy. Measures of shape asymmetry were also obtained by matching the optical anisotropy of samples when unswollen with that observed when swollen with a liquid of known molecular asymmetry. Reasonable agreement was found to hold between the two methods. In contrast, the optical anisotropy of swollen PS was found to be substantially independent of the swelling liquid. The apparent absence of a molecular ordering effect in this case is attributed to the bulky nature of the PS molecule. A marked reduction in optical anisotropy on swelling is ascribed to increased phenyl group motion.
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  • 84
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 999-1024 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Electron spin resonance spectroscopy has been used to study the effects of 15 MeV electrons, x-rays, and ultraviolet radiation on poly-4-methylpentene-1 (TPX) both at 77°K and at room temperature. At least seven identifiably different paramagnetic species are observable in unstabilized oxygen-free TPX after irradiation, and additional species exist in the stabilized grades. The species which predominates under most conditions is interpreted as being due to the loss of hydrogen from a main-chain tertiary carbon atom; interpretations of most of the other species are also given. Oxygen is found to diffuse rapidly into the polymer and to react with the free radicals to form peroxy species. In the absence of oxygen the radiation damage is expected to lead ultimately to crosslinking or double-bond formation, or with oxygen to degradation. The general nature of the free radicals produced by electron or x-ray irradiation is the same, but there are significant differences for ultraviolet irradiation. The observed spectra for irradiated TPX and their interpretations are in good agreement with the spectra and later interpretations for irradiated polypropylene, but are in less satisfactory agreement with the published papers on polybutene-1 and poly-3-methylbutene-1.
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  • 85
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1025-1059 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Native celluloses of various biological origins, as well as regenerated celluloses were examined by electron microscopy after suitable dispersion. In all cases the specimens were found to be composed of a common filamentary unit which is rectangular in cross section and has the approximate dimensions 35 × 20 Å. It is suggested that these are the basic morphological units of cellulose; they are therefore called protofibrils. For protofibrils of regenerated cellulose it is shown that: (1) the molecular contour length greatly exceeds the protofibril length, (2) the mass of the protofibril corresponds to that of a single molecule, and (3) the protofibril length increases with molecular weight. Additionally, high resolution electron micrographs of native and regenerated protofibrils show an apparent axial texture with a periodicity of about 40 Å. From these observations and the knowledge that the molecular chain axis is aligned parallel to the protofibril axis, a model of the protofibril is deduced. The model consists of a ribbon which is pleated on itself so as to form a planar zigzag structure of rectangular cross section. This supersedes a previously proposed model of circular cross section. The structure is composed of a single folded, chain, arranged so that the short extended segments between the folds are parallel to the protofibril axis. The protofibril is thus regarded as the morphological expression of the cellulose molecule. Microfibrils and protofibrils often exhibit kinks, the angle between the kinked portions being 120°. This phenomenon is satisfactorily explained by the protofibril model and in fact provides good support for it. Finally, various properties of cellulose are considered in relation to the model. By contrast with the earlier crystalline-amorphous concepts of cellulose fine structure, it is suggested that protofibrils are completely crystalline structures, and that the properties of cellulose may be understood by considering processes that occur at the level of the protofibril as a unit.
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  • 86
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1149-1151 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 87
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1235-1241 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The literature on polymer morphology contains many studies of structural and orientation changes occurring upon uniaxial stretching of films and fibers, but it has only an occasional reference to such studies on biaxially stretched film. This paper presents data on a structural change due to simultaneous biaxial stretching up to 6 × 6 stretch ratio of quenched linear polyethylene slightly below the melting temperature. At low stretch ratios the b axis of the orthorhombic unit cell orients predominantly in the biaxial plane of stretching or film plane. At higher than 4 × 4 stretch ratio, a second crystal orientation appears which is a (110) orientation in the film plane. Differential scanning calorimetry scans show two melting peaks occurring concurrently with diffraction effects of two crystal orientations. The evidence for two populations of crystals differing in orientation are discussed in the light of current concepts of folded-chain lamellae and their fragmentation with elongation.
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  • 88
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1287-1303 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The viscoelasticity and volume expansion of the raw polymerizate of ethylene-propylene copolymer with vinyl chloride grafts, and of the individual components has been studied. The raw polymerizate (composite) and the pure ethylene-propylene-vinyl chloride graft copolymer were found to consist of two phases. The pure graft copolymer has an ethylene-propylene matrix containing some fraction of poly(vinyl chloride) (PVC) grafts and a microphase with the remainder of the PVC grafts. The raw polymerizate consists of a PVC matrix plasticized with ethylene-propylene chains and a microphase of the ethylene-propylene copolymer. An attempt has been made to calculate the participation of components in microphases and the minimum dimension of the PVC microphase aggregates.
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  • 89
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1333-1339 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The lattice-theory equations for the surface tension of polymer solutions based on the parallel-layer model have been extended to include more than two components. The surface tensions of tetrachloroethylene solutions of some blended polydimethylsiloxane fluids have been measured at room temperature. The results are in nearly quantitative agreement with the theoretical calculations.
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  • 90
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1371-1378 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new relaxation process, explaining the change of elasticity in rubberlike polymers at critical stress (0.1-0.5 kgf/cm2) has been discovered. This process is characterized by the low value of activation energy (weak temperature dependence of relaxation times) and large sizes of kinetic units (strong dependence of relaxation time on stress). Critical stress depend on temperature and for rubberlike polymers turns to zero at 40°-60°C. Mechanism of the phenomena can be explained by the existence of the ordered molecular microregions, creating additional crosslinking points of nonchemical nature with free chains of the network, breaking up at critical stress. Observed phenomena is analogous to the process of forced rubber elasticity of those polymers in glassy state. Critical stress is analogous to the limit of forced rubber elasticity below glass transition temperature.
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  • 91
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1449-1469 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Wide-line NMR spectra have been obtained on an oriented sample of drawn nylon 66 fibers at temperatures between -196°C and 200°C and at alignment angles between the fiber axis and the magnetic field of 0°, 45°, and 90°. At -196°C, 20°C, and 180°C, the complete angle dependence of the NMR spectrum has been measured. The second moments of these spectra have been compared to theoretical second moments calculated for various models of chain segmental motion in an attempt to elucidate the mechanisms involved in the low-temperature segmental motion (γ process) and the high-temperature segmental motion (αc process). In agreement with earlier suggestions, the present results indicate that the γ process consists of segmental motion in noncrystalline regions. The overall decrease in second moment caused by the γ process is consistent with a model in which all noncrystalline segments rotate around axes nearly fixed in space. Furthermore, this decrease shows a pronounced dependence on the alignment angle. It is believed that this is due to tie molecules which become highly oriented along the fiber axis during drawing; their axes of rotation will therefore be nearly parallel to the fiber axis. The segments in noncrystalline entities such as chain folds and chain ends are less well oriented along the fiber axis and make an essentially isotropic contribution to the second moment decrease. The second moment at 180°C indicates the presence of considerable motion in the crystalline regions, and this motion is denoted the αc process. The second moment Sc of the crystalline regions is strongly dependent on the alignment angle, the predominant feature being a relatively high value of the second moment when the fiber axis is directed parallel to the magnetic field. This is in qualitative, but not quantitative, agreement with the motional model recently advanced by McMahon, which assumes full rotation of the chains around their axes. Excellent quantitative agreement with experiment has been obtained by superimposition of rotational oscillation around the chain axis of amplitude roughtly 50°, and torsion of the chains with neighboring CH2 groups oscillating around the C—C bond with a relative amplitude of about 40°. A model in which the chains perform rotational jumps of 60° between two equilibrium sites has also been considered (60° flip-flop motion). A distinction between this model and rotational oscillation has not been possible.
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  • 92
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1525-1529 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 93
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1553-1577 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: As is well known, the chemical potentials of polymer and solvent in solution and, hence, the Flory-Huggins interaction parameter χ can be determined from scattered light intensities from dilute and concentrated solutions of the polymer in the solvent concerned. Preferably, measurements should be performed at temperatures as low as possible, provided the temperature exceeds the cloudpoint for the concentration used. It is shown that the lower the temperature and, consequently the higher the scattered light intensity, the better is the accuracy of the parameters obtained. At each temperature the scattered light intensity shows a maximum at some concentration. Below the theta temperature the ratio of scattered light intensity and concentrations also shows a maximum at some concentration. The values and the concentrations of these maxima for various temperatures enable the maximum of the spinodal to be determined. The spinodal itself can be determined by an extrapolation procedure of the reciprocal scattered light intensities. Measurements have been performed with three narrow-distribution polystyrene samples in cyclohexane. On the basis of the results, χ, and its dependence on concentration, temperature, and molecular weight can be determined to high accuracy.
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  • 94
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1641-1655 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The morphology of high-density polyethylene crystallized under simultaneous pressure and shear in an Instron capillary viscometer has been examined by scanning electron microscopy, electron microscopy, and selected-area electron diffraction. Two distinct fibrous morphologies were observed in these unusually transparent strands. The outer sheath was composed of fibers, 3000 Å in diameter, aligned parallel to the extrusion direction and apparently interconnected by a lamellar cross texture. A highly crystalline ribbon texture composed of fine fibers, 200-250 Å in diameter, dominated the inner core. Sharp-spot electron diffraction patterns obtained from these central ribbons indicated a high degree of c-axis orientation parallel to the fibers and an extended-chain crystal structure. The melting behavior of both irradiated and unirradiated strands examined by differential scanning calorimetry was consistent with the formation of two distinct crystalline morphological units.
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  • 95
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1681-1691 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The influence of the nature of exchangeable cations on the tacticity of poly(methyl methacrylate) (PMMA) prepared from montmorillonite-MMA adsorption complexes was investigated. The strength of ion-dipole interactions was estimated either by the value of the electrostatic interaction potential or by the value of the carbonyl-stretching frequency shift. It was shown that Pi, the percentage of isotactic triads in the polymer, increases with increasing strength of the ion-dipole interactions, while the persistence ratio and the mean length of closed isotactic (or syndiotactic) sequences remain essentially unchanged regardless of the nature of the cation. It was shown that values of Pi may vary from 0.15 for weakly interacting ions to 0.5 for strongly interacting ones, reaching at the upper limit the value calculated from the model proposed in a previous paper, thus confirming its validity.
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  • 96
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1693-1702 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Differential thermal analysis (DTA) of some commercial nylons has disclosed some anomalous phenomena with respect to the glass transition, generally considered to occur at 40-50°C. On the first heat cycle the transition occurs normally. On cooling, however, no corresponding transition occurs, and on an immediate rerun the transition has disappeared. If another DTA thermogram is made after a few hours, the transition begins to reappear, but at a temperature lower by a few degrees. After about five days rest, the transition is again normal in size and temperature. On annealing at 75°C, the 43°C transition is pushed up to about 92°C. On resting after annealing, transitions appear at both 40 and 92°C. These phenomena are explained in terms of the slow formation of a hydrogen-bonded network in the amorphous regions of the polymer. It is the disruption of this network that is normally considered to be the glass transition in nylons. The network is slow in re-forming because of problems involved in matching up potential hydrogen-bonding sites, which are, of course, distributed at intervals along the polymer chain. The temperature at which the network is disrupted is apparently dependent not so much on the ratio of bonding to nonbonding sites, as on the temperature at which it was formed.
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  • 97
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1793-1805 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Detailed critical examinations of three aspects of nitric acid treatment of polyethylene are reported. (1) The endgroups introduced by the nitric acid are examined. It is concluded that in samples degraded to a single-crystal traverse stage, carboxyl features only as endgroup, and conversely each chain-end is terminated by such a group. Consequently, the carboxyl content can be used for quantitative characterization of the cut chain length. The function and position of the nitro group remains unexplained. (2) The morphological selectivity of the nitric acid-induced degradation is scrutinized. It is concluded that the crystal core is attacked and thinned by the acid; the slowing down of the reaction is principally due to accumulation of reaction products. Accordingly, the usual distinction between a vulnerable amorphous layer and a resistant crystal core is not justified on the basis of such degradation experiments. It follows that meaningful structural information is obtained only when the relevant crystal properties are studied as a function of chain cutting, assessed from the molecular weight distribution (GPC), as opposed to that of degradation time alone. (3) The role of sample consistency and reagent strength has been examined. It is demonstrated that for the reaction to be sufficiently uniform throughout the sample for the results to be meaningful, the reaction rate has to be slow compared to the rate at which the reagent diffuses into the specimen. To realize these conditions, finely dispersed samples and weak reagents were found to be favorable
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  • 98
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1871-1885 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Several samples of a copolymer were examined by means of equilibrium centrifugation in a density gradient. The results for the samples without compositional distribution (homogeneous polymers) were used to determine the relation between the chemical composition and the distance from the center of rotation. For one of the homogeneous polymers a quantitative analysis of the schlieren curve was made in order to show the kind of accuracy that can be achieved. For the inhomogeneous polymer it was found that the schlieren curve could, in principle, be described quantitatively by the assumption that fluctuations in composition are independent of fluctuations in molecular weight, but on this basis the average square of the fluctuations in composition is more than four times smaller than the value derived from chromatographic data. A more satisfactory explanation of the experimental results is provided by assuming a linear correlation between average molecular weight and composition, but it is not claimed that this is necessarily the only model that explains the data.
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  • 99
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1887-1905 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Time-dependent, apparent heat capacities of glucose, poly(vinyl chloride), polystyrene, selenium, poly(methyl methacrylate), and poly(2,6-dimethyl-1,4-phenylene ether) in the glass transition region were determined by differential thermal analysis. The thermal history was set by linear cooling at rates between 0.007 and 160°C/min. Linear heating for analysis was carried out at rates between 0.3 and 600°C/min. Average activation energies of 52, 81, 90, 54, 77, and 108 kcal/mole, respectively, were evaluated by using the hole theory of glasses previously developed. Within experimental limitations all data could be described quantitatively by the theoretical expressions using only one parameter, the number of frozen-in holes, to described the thermal history. Experimental and theoretical limitations are discussed.
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  • 100
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1915-1918 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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