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  • 1965-1969  (1,941)
  • Physics  (1,849)
  • Cat  (55)
  • Psychopharmacology  (37)
  • 101
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 497-513 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Triplet → singlet energy transfer in nylon 66 film (donor) dyed with proflavine (acceptor) is demonstrated by a decrease of the nylon phosphoresence lifetime and an increase in the proflavine delayed fluorescence/nylon phosphoresence ratio with increasing proflavine concentration. Although the observed donor phosphorescence decay is apparently exponential, the transfer is probably via a long-range dipole-dipole (Förster) interaction, rather than by triplet exciton migration. Arguments are advanced to support this view. Proflavine delayed fluorescence produced by a direct excitation process is also observed. The decay time for this process is roughly an order of magnitude less than that for the sensitized process. All emission intensities are shown to vary linearly with exciting light intensity. Finally, temperature dependence of proflavine delayed fluorescence under different excitation conditions is shown. The efficiency of direct excitation process increases markedly near -50°C as the temperature is increased; the sensitized delayed fluorescence intensity follows that of the nylon phosphorescence with increasing temperature, as expected.
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  • 102
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 587-592 
    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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  • 103
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 601-608 
    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 Tg of several fluorine-containing polymers were determined by use of the differential scanning calorimeter. Values between -3 and 230°C were obtained. In polymers of α-olefins, Tg increases with the fluorine content of the backbone and the length of the n-perfluoroalkyl branch. In styrene polymers Tg also is higher if the backbone contains fluorine but nearly the same Tg's are found for polymers with phenyl and pentafluorophenyl groups. Saturated polymers of perfluoro-α,ω-dienes have lower Tg's than polyperfluoro-α-olefins. The Tg's of chloroperfluoropolymers are higher than those of perfluoropolymers. Polyperfluoropentadiene-1,3 has the lowest Tg of the polymers examined. Polyperfluoropentadiene-1,3 forms by 1,4-addition.
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  • 104
    Electronic Resource
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 667-674 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Drawn poly(ethylene terephthalate), PET, yarns have been heated for 1 min in silicone oil. The resulting samples were studied by x-ray diffraction and mechanical properties were measured. The results suggest that drawn PET consists of highly extended molecules essentially parallel to one another, with few folds present. On heating, chain folding occurs. This model is very similar to that proposed by Dismore and Statton for drawn nylon 66 yarns.
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  • 105
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 143-151 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A theoretical discussion is presented on the mechanisms by which an isolated pulsating air bubble in a viscoelastic solid dissipates its energy. The analysis is limited to the situation where the amplitude of motion is assumed to be sufficiently small that the stress strain relations may be described by linear equations with convected differentiation replaced by ∂/∂t. The theoretical thermal, radiation, and viscous damping constants are calculated for resonant air bubbles in unvulcanized natural rubber; however, the results are typical of elastomers in general.
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  • 106
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 231-240 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The birefringence of several biaxially oriented polypropylene films swollen with a number of fluids has been measured and found to exhibit a minimum when plotted against the fluid refractive index, as predicted by the theory of Wiener. However, a discrepancy in the form birefringence behavior is observed when samples of different degrees of crystallinity but the same total birefringence are compared. These results are interpreted in terms of Bullough's theory and suggest that this discrepancy arises because of different morphologies. A refractometric technique was employed that makes possible the simultaneous determination of birefringence and the volume fraction of fluid.
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  • 107
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 153-161 
    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 polyethylenes formed upon polymerization by γ-radiation below the melting point in various reaction media was investigated by using electron microscopy and scanning electron microscopy. When the polymerization was carried out in bulk at 30°C and in methanol, the polymer was fibrillar, and a small-angle x-ray scattering curve of the polymer did not indicate the existence of a long period. This suggests that the chains in the crystals have an extended conformation. When the polymerization was carried out in the presence of xylene at 30°C, platelet crystals having a folded structure were obtained. It was thus shown that the morphology of the growing polymer crystals is very much affected by the solubility of the polymer in the reaction medium. The effect of stirring during polymerization on the crystalline morphology was also studied.
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  • 108
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 209-217 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The intrinsic viscosity of a polymer in a solvent mixture is related to the excess free energy of the solvents. Intrinsic viscosities at different temperatures are obtained for poly-2-vinylpyridine-chloroform-ethyl alcohol, poly(methyl methacrylate)-chloroform-ethyl alcohol, polystyrene-cyclohexane-benzene, polystyrene-dioxane-chloroform, and polystyrene-cyclohexane-ethanol. Qualitative, but not quantitative, agreement is found between theory and experiment.
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  • 109
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1315-1328 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The circumstances of the formation of kink bands have been investigated with a newly designed shearing device and light and electron microscopes. Kink bands having sharp edges and reflection symmetry about the edges were formed and studied in the two crystalline polymers, high-density polyethylene and isotactic polypropylene, but could not be formed in the two glassy polymers, poly(4,4′-dioxydiphenyl-2,2-propane carbonate) and poly(2,6-dimethylphenylene oxide). The characteristics of the oriented polymer that promote kink bands seem to be easy slip along the orientation axis, and resistance of the oriented fibrils to length changes. Kink bands were found to initiate at sites of shear stress concentration, where the fibrils are first deformed into an S-shaped curve, that then tightens and finally collapses into kinks.
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  • 110
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1303-1314 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Column chromatographic fractionation of polystyrene was carried out with the methyl-ethyl ketone-methanol system, and effects of various experimental conditions on the fractionation efficiency were studied. For samples with molecular weights below about 6 × 105, neither the temperature gradient (0.7°C/cm), nor the flow rate of solvent (30-270 ml/hr) seriously influences the fractionation efficiency. The effect of temperature gradient becomes apparent only in the high molecular weight region and only if the gradient of the solvent composition is too steep. High flow rates (ca. 125 ml/hr) clearly affect the fractionation efficiency for a high molecular weight sample (Mw = 5.46 × 105). Precipitation chromatography for the fractionation system was calculated from the phase equilibrium data according to the mass transport equation proposed by Schulz et al. The theoretical analysis gives support to the observed dependence of the temperature effect on molecular weight. Comparison of the observed and theoretical relations between elution volume and molecular weight of the fraction, on the other hand, indicates that the process of fractionation is simply elution of polymer off the support without reprecipitation. Certain conditions of polymer deposition on the support are required for optimal results.
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  • 111
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1435-1438 
    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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  • 112
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1461-1472 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Thermal analysis has been carried out on drawn nylon 6 filaments annealed at various temperatures between 150 and 210°C and then methoxymethylated to various degrees. It is shown that the melting point inherent to the morphology of drawn nylon 6 can be obtained from samples in which the reorganization of defect crystallites in the course of thermal analysis is prevented by a proper degree of methoxymethylation of amorphous regions. The melting point thus obtained is in linear relation with the reciprocal crystallite size in the direction of fiber axis which has been obtained from small-angle x-ray data and crystallinity. The extrapolation and the slope of this linear relation give the equilibrium melting point of nylon 6 as 245°C and an end-surface free energy of 42 erg/cm2. The results seem to provide strong support for the presence of chain-fold surfaces in the drawn and annealed polymers.
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  • 113
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1489-1494 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Raman scattering of nonplanar (form 2) poly(vinylidene fluoride) (PVF2) is described. Unique Raman bands not observed in the infrared spectra are found at 2973, 1437, 1327, 1198, and 1059 cm-1. Band assignments are discussed by comparing infrared and Raman spectra of form 2 PVF2.
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  • 114
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1705-1719 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The temperature dependence of relative modulus observed in filled thermoset, thermoplastic, and polyelectrolyte salt matrices is explained on the basis of induced stresses produced by the differences in the thermal expansion coefficients of the constituent materials. The analysis is based on the assumption that the modulus of the matrix in a filled polymer is less than that of the unfilled polymer. The temperature dependence of relative modulus is expressed as a function of the difference in thermal expansion coefficients, the volume fraction, the relative modulus in the unstressed state, and mechanical properties of the phases. Agreement is good between the analysis and experimental results for three systems: epoxy and glass, polyethylene and wollastonite, and a polyelectrolyte salt with mica and asbestos.
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  • 115
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1785-1809 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Infrared spectroscopic studies have been made of mixed crystals of linear polyethylene and perdeuteropolyethylene. On the basis of normal vibration analyses by Tasumi and Krimm it had been shown that the study of crystal splittings of internal chain modes in such mixed crystals could provide information on the geometry of chain folding. The present results, which include a study of n-paraffin (C36) mixed crystals, confirm these predictions. They show that (110) folding predominates in dilute solution grown crystals, and that this is transformed to (200) folding in melt-crystallized polymer. Folding with adjacent re-entry is favored, a random re-entry model being clearly eliminated.
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  • 116
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1883-1894 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Data existing in the literature for the spherulitic growth rate of molecular weight fractions of linear polyethylene, poly-(tetramethyl-p-silphenylene)siloxane, and trans-1,4-polyisoprene have been analyzed according to nucleation theory on taking into account the influence of chain length on the free energy of fusion. All three polymers display very similar behavior in that the interfacial free energy reaches an asymptotic value at high molecular weights, decreases as the molecular weight is lowered, and appears to also reach an asymptotic value at low molecular weights. Although the changes in the interfacial energy with molecular weight are quite distinct, the relative change is much less than has been previously reported when a molecular crystal analysis is used. The same general behavior observed points out the dominating influence of the chain-like character of the molecules in governing the growth rate.
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  • 117
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1111-1115 
    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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  • 118
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1187-1195 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Extensive studies of the kinetics of spherulitic crystallization have been made on fractionated samples of TMPS. An analysis of these results reveals that a two-dimensional growth rate mechanism is a more likely mode of growth than a three-dimensional one. This conclusion is substantiated by experimental evidence from optical microscopy and light scattering from within spherulites. The crystallite end surface energy is found to increase as the molecular weight is raised.
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  • 119
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1275-1278 
    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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  • 120
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A modus operandi is developed for determining the molecular structure of hydroxypropylcellulose (HPC), and characterizing, in quantitative terms, the morphological changes occurring when a water-cast film of the polymer is deformed. This involves the application of the following eleven different physical measurements: wide-angle x-ray diffraction, differential scanning calorimetry, density, melt rheometry, infrared spectroscopy, refractive index, birefringence, sonic modulus, small-angle light scattering, optical and electron microscopy. In addition, a computer was utilized as a mathematical diffractometer. Morphologically, water-cast HPC was observed to have structure at all levels, from the molecular to the supermolecular. The HPC molecule has a backbone of anhydroglucose units twisted into an irregular 31 helix. Intramolecular hydrogen bonding of the poly(propylene oxide) side chains leads to a stiff, rodlike molecule. The molecules are packed into microfibrillar crystallites 470 Å long and 34 Å in diameter. The microfibrils in turn, associate into supermolecular rodlike structures. The structural rearrangements that occur at each morphological level during deformation of HPC film are quantitatively examined and described.
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  • 121
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1329-1355 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Mechanical relaxation has been studied at 0.67 cps in linear polyethylene (LPE) and polytetrafluoroethylene (PTFE) between -190 and -20°C. Specimens were prepared by use of various thermal treatments to produce in LPE a range of crystalline fractions from 0.690 to 0.825 and in PTFE from 0.615 to 0.870. An empirical theory is proposed relating the modulus of the crystalline-amorphous composite solid to the moduli and the volume fractions of the two phases. The empirical theory is shown to be in accord with the bounds of Hill and of Hashin and Shtrikman. The theory is used to determine the magnitudes of the crystalline and amorphous components of the low temperature relaxations in LPE and PTFE from measurements of logarithmic decrement and shear modulus. In PTFE the γ relaxation occurs in the amorphous fraction alone. In LPE the γ relaxation is a composite one, formed from the superposition of a small crystal relaxation and a large amorphous relaxation. For the crystal relaxation in LPE the ratio of relaxed to unrelaxed modulus equals 0.78; for the amorphous relaxation, the ratio equals 0.23. In a specimen of LPE with crystal fraction 0.69 the crystal contribution to the relaxation is 25% of the total. The magnitude of the unrelaxed modulus of the crystal fraction of LPE (modulus of polycrystalline LPE at -190°C) is in reasonable agreement with theoretical calculations of Odajima and Maeda.
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  • 122
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1385-1392 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Shear viscosity and dielectric dispersion measurements have been made on a series of concentrated solutions of poly-p-chlorostyrene in toluene, chlorobenzene, and diethylbenzene, as well as on the pure polymer. It is found that the product ηνm/T is nearly temperature-independent in the present range of measurement (30 ≤ νm ≤ 30 ≤ 104 Hz), where νm is the frequency at which the dielectric loss maximum occurs. For the pure polymer, ηνm (200/T) is 1011.5 poise/sec. This leads to a segmental jump distance of 5 Å. Although the results in this range correspond quite well to the concept of a segmental friction constant determined by the matrix viscosity, deviations appear as the apparent energy of activation for viscous flow decreases below 13 kcal/mole. There is reason to believe that these deviations reflect the increasing importance of bond rotation barriers at low matrix viscosity. It is speculated that the damped torsional oscillator interpretation of f0 proposed by Tobolsky will become valid in systems still more fluid.
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  • 123
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new light-scattering experiment which allows a direct determination of the conformation of macromolecules deformed in flow is described. Light-scattering relationships based on the interference function are developed, and results of an experimental study are detailed. The deformed conformation of high molecular weight polyisobutylene was determined in a Couette-type shear field. Decalin was the solvent. Variables investigated were the shear rate (0 to 600 sec-1), the polymer molecular weight (1.0 × 107 to 1.6 × 107), and the polymer concentration (2.0 × 10-4 to 8.0 × 10-4 g/cc). Conformation variables determined were the orientation of the molecule in the shear field and its maximum and minimum extension ratios in the plane defined by the direction of flow and the direction of the shear rate. The deformation of the macromolecule was found to be markedly discrepant when compared to the dynamic macromolecular models which assume complete coil flexibility, and more closely in agreement with the recent theories of Cerf, developed for nonfree-draining coils which exhibit a finite internal viscosity.
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  • 124
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1439-1443 
    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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  • 125
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1473-1481 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The mechanical and dielectric low temperature absorptions of poly(vinyl chloride) (PVC) and several modified PVC's have been studied over the temperature range from -60 to +60°C. with some tests extending to -150°C. and others to +170°C. The results indicate that the low-temperature absorption near -50°C (β2 absorption) decreases in intensity with chlorination, while the absorption at a higher temperature near 0°C (β1 absorption) decreases in intensity with hydrogenation. The apparent activation energies of the β1 and β2 absorptions were calculated to be 16 kcal/mole and 10.7 kcal/mole, respectively. Besides, the β2 absorption markedly decreases in intensity with addition of plasticizer, while the intensity of β1 absorption is not much affected by increasing plasticizer content. From these results, the β1 and β2 processes are concluded to be the results of molecular motion in crystalline and amorphous region in PVC, respectively. For samples of reduced Cl content, another low-temperature absorption was located near -120°C (γ absorption) and attributed to the presence of short sequences of ethylene units. It has also been observed that the temperature location of the high temperature absorption near 100°C (α absorption) shifts linearly to higher temperature with increasing chlorine content and to lower temperature with increasing hydrogen content.
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  • 126
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1513-1523 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Six homologs of the cellulose triester series were found to exhibit, in general, three second-order transitions as determined dilatometrically. A parallel study of torsional modulus versus temperature revealed one glass-rubber transition, which allowed molecular assignment of one of the above. The dependence of the remaining two transition temperatures on length of the ester group permits some speculation with regard to their origin. The glass-rubber and secondary transitions exhibit an inversion for cellulose trivalerate and higher homologs, the two secondary transitions occurring at temperatures higher than the glass-rubber transition. A possible explanation for this anomaly in terms of side-chain crystallization is discussed.
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  • 127
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1639-1649 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The melting transitions of both crystalline forms of trans-1,4-polyisoprene, as detected by differential thermal analysis, have been identified by attendant studies with optical microscopy and x-ray diffraction. The lower-melting (LM) form melts initially at a temperature which depends upon the crystallization temperature but which, under our experimental conditions, is between 45 and 53°C. If recrystallization is allowed to occur, the apparent final melting point, which depends upon the recrystallization temperature, is about 58°C. The initial melting point of the higher-melting (HM) form, also crystallization temperature-dependent, is upwards of 57°C. Under the most easily accessible experimental conditions, it may be obscured by the final melting of the LM-form. The apparent final melting point of the HM form is approximately 66°C. Conversion of the LM form into the HM form occurs only by fusion and crystallization. No evidence of a solid-solid transition was found. The rate of conversion is governed principally by the rate of nucleation at the conversion temperature. If fusion of the LM form is incomplete, recrystallization of the LM form takes place instead of conversion to the HM form.
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  • 128
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1681-1694 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Creep compliance data, J(t), at 35°C for poly(β-hydroxyethyl monomethacrylate), crosslinked by ethylene glycol dimethacrylate in a range of concentration C from 0.0855 to 2.053 × 10-4 mole/cm3 and swollen to various degrees in diluents, were examined for time-concentration superposition. From the dependence of time scale shift factors on v2, the volume fraction of polymer, free volume parameters were calculated for two samples with C = 0.0855 × 10-4 and 0.136 × 10-4 mole/cm3, swollen in the range of v2 from 0.134 to 0.591. Special attention was given to the magnitude of the shift factor on the log J(t) axis and its dependence on concentration, which was found to depend substantially on the crosslinking and the swelling degrees of the samples. This shift was approximately log v2 for lightly crosslinked samples, swollen to a small degree, measured in the neighborhood of the main transition. For higher degrees of crosslinking and/or swelling, the shift was much less and for the most highly crosslinked networks swollen to equilibrium it was even negative. The correction appears to be very sensitive to the strain of the effective chains and to the location on the time scale with respect to the transition and rubberlike zones of viscoelasic behavior. It was found that the parameters of the WLF equation calculated in our previous study from the time-temperature superposition of the creep curves in the rubber-glass transition are valid also for the rubberlike region.
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  • 129
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1775-1783 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A systematic study of factors affecting the GPC separation showed that peak spreading with increasing flow rate was much less than predicted from the Van Deemter equation. Viscous fingering decreased and peak symmetry improved at increased flow rates. As a result, fast GPC analysis was shown to be readily attainable through optimization of operating parameters.
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  • 130
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 279-284 
    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 birefringence on light scattering is considered, using classical theory. It is shown that in conjunction with polarized light scattering, the use of birefringence can aid in the reduction of experimental errors; also how new checks on theory can be made. The treatment is applied to scattering from simple gaseous molecules and thin polymeric films.
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  • 131
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 433-462 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The intrachain and interchain vibrations below 900 cm-1 of polydimethylsiloxane (PDMS) have been studied by slow neutron inelastic scattering. A composite motion observed at +25°C for the methyl groups corresponds to nearly free rotation about the threefold axis of symmetry together with a large-amplitude rotation of the entire methyl group. At -123°C, rotation about the threefold axis evolves to a torsional oscillation. The large-amplitude rotation evolves to the skeletal vibrations of a helical conformation. Vestiges of the cooperative skeletal vibrations of the conformation at -123°C persist into the 25°C spectrum. The results indicate the presence of interrupted helical conformations at 25°C, which result from thermal disordering of the low temperature helices. The effects of crosslinking, low molecular-weight oils, and silica filler on the freedom of the methyl group motions and on skeletal vibrations have been determined. The effects of different crosslinking agents and different relative amounts of filler and oil on both the macroscopic physical properties and the observed molecular motions of PDMS can also be interpreted in terms of an interrupted helix.
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  • 132
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 475-481 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Experiments in which an oscillatory shear flow is superimposed on a steady state shear flow were performed on polyethylene melts by the use of a cone and plate type rheogoniometer. The phase difference between oscillatory shear stress and shear strain increases in all cases and for all frequencies with the increase of the superimposed shear rate. Between ω0, the frequency at which the phase difference is π/2 and the steady shear rate \documentclass{article}\pagestyle{empty}\begin{document}$ \dot \gamma $\end{document}, as found by Booij for polymer solution, the relation ω0 = 1/2 \documentclass{article}\pagestyle{empty}\begin{document}$ \dot \gamma$\end{document}. holds also for polyethylene melts. The significance of this relation is discussed briefly from the viewpoint that the entanglement density decreases with the increase of the imposed shear rate.
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  • 133
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 37-45 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The well known procedure of determining the degree of crystallinity by means of measuring the density presupposes the knowledge of both the densities ρc and ρa of the crystalline and of the noncrystalline regions. By combination of small-angle and wide-angle x-ray scattering and of density measurements it can be shown that this method is not justified in the case of drawn polyethylene if the values of ρc and ρa known from isotropic material are used. Both ρc and ρa depend considerably on annealing and drawing conditions. In addition the effective density ρc* of the more densely packed phase in a two-phase structure is much lower than the value ρc calculated from the positions of the x-ray reflections due to a large number of lattice defects. This conclusion is based on the results of three independent sets of experiments: determination of the mean-square fluctuation of density 〈η2〉 by means of x-ray small-angle scattering; x-ray wide-angle measurements of the positions of the crystal reflections and of the halo arising from the noncrystalline regions; and comparison of densities and long periods of samples treated at various annealing temperatures.
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  • 134
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 123-142 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Isothermal and nonisothermal spherulitic crystallization in even-odd and poly(ω-aminocarboxylic acids) has been studied for a range of fusion conditions and solidification temperatures. The variety of spherulites so formed are classified mainly by optical microscopy. It is found that polyamides with similar types of repeat units generally exhibit similar morphological features under corresponding crystallization conditions. The basic patterns are illustrated in the text. Changes in spherulitic birefringence with temperature are also discussed. In some cases, at temperatures not far below the polymer melting point, platelet-like crystalline aggregates are formed in thin film preparations. These platelets exhibit properties characteristic of single crystals.
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  • 135
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 483-495 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The peak separation in gel-permeation chromatography (GPC) is attributed to the contributions of the steric exclusion and the lateral diffusion processes. The advantage of using the distribution coefficient KGPC of the solute molecule in interpreting the GPC separation mechanism is assessed. The physical significance of KGPC and its relation to measurable GPC parameters are examined in detail. A simple mixing experiment for determining the exclusion effect is described. The results of this experiment, as well as those of the flow rate study, show that the exclusion effect plays the primary role in GPC peak separation. For a column packed with Bio-Rad porous glass of 200 Å designation, the diffusion effect does not contribute significantly to peak separation. However, for the case of a Waters Associates column packed with polystyrene gel of 104 Å designation, both the exclusion and the diffusion effects are shown to be important. A diffusion theory which includes the concept of a restricted diffusion coefficient is proposed to interpret the diffusion effect observed in the polystyrene gel column. The results of the theoretical calculation are found to agree with the observed flow rate dependence of the calibration curve.
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  • 136
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 537-549 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Thermogravimetric analyses (TGA) of catalyst-free polydimethylsiloxanes (PDMS) have been carried out in controlled atmospheres and a kinetic analysis of the results has enabled the various decomposition processes to be separated and identified. The calculated activation energy for thermal depolymerization is 42 ± 3 kcal/mole, while thermo-oxidation has an apparent activation energy of 30 ± 2 kcal/mole. Quantitative analyses of the major degradation products and molecular weight distribution studies of the residues from degradation studies under isothermal conditions have shown that in vacuo, PDMS fractions depolymerize to cyclic dimethylsiloxanes and low molecular weight linear residues by a randomly initiated mechanism which, it is postulated, involves the formation of an intramolecular, cyclic, four-centered transition state followed by siloxane bond rearrangement. This mechanism is a basic property of linear PDMS fractions and is independent of molecular weight. Molecular weight distribution (MWD) changes observed from further isothermal investigations on hydroxy endblocked PDMS fractions, have shown the presence of a chain-lengthening process in vacuo below the depolymerization temperature. This process, with an apparent activation energy of 8.6 ± 1 kcal/mole, is attributed to the intermolecular condensation of terminal hydroxyl groups.
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  • 137
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 575-586 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The intrinsic viscosities of fractions of poly(ethylene oxide) in the molecular weight range 1.5 × 103 to 106 have been measured at 25°C in benzene, carbon tetrachloride, and acetone; at 35°C in 0.45M aqueous potassium sulfate; and at 50°C in methyl isobutyl ketone and diethylene glycol diethyl ether. The latter three are practically theta solvents. The value of (r02/M)1/2 for poly(ethylene oxide) is calculated to be 0.84 Å from the molecular weights of the high molecular weight fractions, and their intrinsic viscosities in the theta solvents and acetone. Erroneous values result if the usual methods of determination are applied to the data obtained for the low molecular weight (〈104) fractions or to the intrinsic viscosities in the very good solvents, benzene and carbon tetrachloride.
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  • 138
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 609-633 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Molecular weight determinations by light scattering and osmometry and intrinsic viscosity measurements were made in various solvents on fractions of styrene-methyl acrylate copolymers with different compositions and on acrylate homopolymers prepared by free-radical reaction. Relations between intrinsic viscosity [η] and molecular weight M thus established are compared with those reported by other authors. 2-Methylcyclohexanol was found to be a theta solvent for the copolymers and both parent homopolymers, and isoamyl acetate was a theta solvent for poly(methyl acrylate). From theta point viscosity data obtained with these solvents, unperturbed chain dimensions were estimated. The results are compared with the unperturbed dimensions estimated from the [η]-M relations obtained in good solvents. On the basis of the experimental data it was found that the unperturbed dimension depends linearly on the copolymer composition, in contrast to the case of styrene-methyl methacrylate copolymers. Composition dependences of the theta temperature and of the parameter describing the long-range interactions between nonadjacent segments in polymer chains were investigated. The result implies that long-range interactions between monomeric units never disappear even when those between the same monomeric units vanish. The Huggins constant for copolymer is discussed in terms of the excluded volume variable.
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  • 139
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 635-658 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Stress-strain and rupture data were determined on an unfilled styrene-butadiene vulcanizate at temperatures from -45 to 35°C and at extension rates from 0.0096 to 9.6 min-1. The data were represented by four functions: (1) the well-known temperature function (shift factor) aT; (2) the constant strain rate modulus, F(t,T), reduced to temperature T0 and time t/aT, i.e., T0F(t/aT)/T; (3) the time-dependent maximum extensibility, λm(t/aT); and (4) a function Ω(χ) where χ = (λ - 1)λm0/λm, in which λ is the extension ratio and λm0 is the maximum extensibility under equilibrium conditions. The constant strain rate modulus characterizes the stress-time response to a constant extension rate at small strains, within the range of linear response; λm is a material parameter needed to represent the response at large λ; and Ω(χ) represents the stress-strain curve of the material in a reference state of unit modulus and λm = λm. The shift factor aT was found to be sensibly independent of extension. At all values of t/aT for which the maximum extensibility is time-independent, the relaxation rate was also found to be independent of λ. These observations indicate that the monomeric friction coefficient is strain-independent over the ranges of T and λ covered in the present study. It was found that λm0 = 8.6 and that the largest extension ratio at break, (λb)max, is 7.3. Thus, rupture always occurs before the network is fully extended.
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  • 140
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    Notes: The ultimate properties of an unfilled styrene-butadiene rubber vulcanizate in equal biaxial tension were determined by inflating a circular membrane into a bubble. Tests were made at several extension rates (evaluated at the pole) from about 0.15 to 4 min-1 and at temperatures from -43 to 90°C. The stress in the vicinity of the pole when rupture occurred was evaluated from the pressure, the radius of curvature, and the extension ratio λ, the latter two quantities being obtained from photographic data. Below 70°C, the ultimate extension ratio λb is approximately 5.2 and is essentially independent of extension rate and temperature, in striking contrast to the behavior in simple and constrained biaxial tension (pure shear). Likewise, the rupture stress is manyfold greater than in either simple or constrained biaxial tension. From the extremum points of failure envelopes, the maximum extension ratio (λb)max in equal biaxial tension is 5.7 and in simple tension is 7.2. An examination of ruptured membranes showed that, except at 70 and 90°C, rupture began away from the pole in a region where the stress state is unequal biaxial tension. Hence, values of the ultimate properties in truly equal biaxial tension are no doubt somewhat greater than those obtained from the membrane tests. However, it is shown that (λb)max in truly equal biaxial tension must be lower than that in simple tension by at least 10%. A consideration of rupture data in simple, constrained biaxial, and equal biaxial tension leads to the conclusion that no simple failure criterion is applicable for interrelating data obtained under the several states of combined stress. The rupture patterns and factors that affect the site of rupture initiation and the mode of crack growth are also discussed.
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  • 141
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 735-742 
    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, at the yield stress, glassy polymers exhibit viscous flow which is in agreement with the generalized theory of Eyring. The study of the yield stress over a wide range of temperatures and strain rates provides evidence on the secondary transitions found by other methods. From our measurements we conclude that every secondary transition corresponds to the liberation of one of the degrees of freedom of a segment of the main chain.
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  • 142
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 751-751 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 143
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 795-807 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dynamic mechanical properties determined with a torsion pendulum were used to ascertain the glass transition temperature Tg of poly-ε-caprolactone. By measurements on compatible blends of poly-ε-caprolactone and poly(vinyl chloride), the Tg of amorphous poly-ε-caprolactone was shown to be 202°K at about 1 cps. This is 16°K lower than the Tg of annealed, crystalline polymer. The blend transition data were well fitted by both the Fox and the Gordon-Taylor expressions. The Fox expression was also used to describe the decrease from 233°K of the secondary low-temperature relaxation due to poly(vinyl chloride) by assuming the low temperature relaxation of poly-ε-caprolactone, 138°K, was responsible for the decrease in the blends. The 138°K relaxation due to poly-ε-caprolactone was decreased when more than 50% poly(vinyl chloride) was present.
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  • 144
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 829-844 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(vinyl chloride) sheet was oriented by hot drawing. The yield behavior of the oriented sheet was then investigated under uniaxial tension at room temperature as a function of the angle between the tensile axis and the molecular alignment direction. The onset of yield was localized in deformation bands. The variation of yield stress with direction and the direction in which the deformation bands formed were found to be satisfactorily accounted for in terms of a yield criterion based on that of von Mises, provided that a term representing internal compressive stress in the molecular alignment direction was included. The internal stress was found to increase from zero with increasing draw ratio of the prior hot drawing. It is pointed out that other workers have found polymers to obey the yield criterion of Coulomb rather than that of von Mises.
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  • 145
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 879-887 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Fickian diffusion coefficient of methylene chloride in a glassy epoxy polymer is calculated with the use of Crank's model of discontinuous change of D with concentration C. The diffusion constant is obtained as 1.93 × 10-6 cm2/sec. The swollen layer behind the advancing solvent front is essentially in the rubbery state of the same polymer. The case II swelling by benzene is discussed in terms of a convective transport arising from the partial stress (internal) tensor of the penetrant. The superposition of Fickian and case II diffusion found with mixtures of methylene chloride and benzene is also discussed briefly.
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  • 146
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 929-945 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: “Regular” sequence copolymers having the structure {[—CH2—C(CH3)(C6H5)—]m(CH2—CH2)n}p with relatively small values of m and n were prepared by means of “living” polymerization techniques. The intrinsic viscosities of fractions of these copolymers were obtained in various solvents including a theta solvent. The molecular weights of these fractions were determined by the Archibald ultracentrifugal method. The results show that the intrinsic viscosity-molecular weight relations of the regular sequence copolymers are affected not only by the average composition of the copolymer, but also by the sequence length in the copolymer molecule. It is suggested that the effective conformation of a chain element in the copolymer is not always the same as that in the homopolymer.
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  • 147
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1619-1621 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 148
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1651-1667 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The plastic deformation of poly-4-methylpentene-1 (P4MP1) crystals on a unidirectionally drawn substrate has been investigated by electron microscopy. In addition to cracks spanned by fibrils and buckling perpendicular to the stretch direction, both features found in deformation studies of other polymers, a unique slip mechanism leading to sectorization of P4MP1 crystals is observed; deformation was also found to occur by means of localized lamellar thinning. The exact type of plastic deformation occurring in P4MP1 crystals is found to depend on the orientation of the lamellae with respect to the tensile axis. Some evidence for a periodicity on the fibrils studied is given.
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  • 149
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1669-1679 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A method for evaluating the relaxation time as a function of both temperature and volume from volume contraction experiments, as proposed by Kovacs, was experimentally examined by using monodisperse poly-α-methylstyrene samples of various molecular weights and blends. It was concluded that his theory can be successfully applied to the present experimental data, though his two different approximations give somewhat different values of the shift factor for the time-temperature superposition of volume contraction data. A difference was observed between the temperature dependence of the shift factor of monodisperse polymers and that of blends.
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  • 150
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    Topics: Chemistry and Pharmacology , Physics
    Notes: Electron microscopic textures of A-B type block copolymers of styrene and isoprene cast from several solvents were investigated by means of the osmium tetroxide fixation technique. The two-phase structure, i.e., the semimicro heterogeneous structure due to the microphase separation of block segments, was observed to change systematically with the fraction of block segments and the kind of solvent. Three types of fundamental domain structure were found. With the assumption that domain structure originates from micellar structure at a critical concentration in relatively dilute solution during solvent casting, the formation of the three types of domain structure and the sizes of their elements were treated in terms of the equilibria governing the formation of micelles at the critical concentration. This analysis takes into account such thermodynamic and molecular parameters as the incompatibility between the A and B segments, the solvation of the segments, the casting temperature, the total chain length of the block copolymer, and the weight fraction composition of the block copolymer. It was concluded that the block segments are preferentially oriented along the direction perpendicular to the interface between the two phases. This particular orientation-aggregation of the block segments must make the bulk properties of the block copolymer much different from those of merely mechanical mixtures of the corresponding homopolymers, even if the same semimicro heterogeneous structures are formed in the mechanical mixtures.
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  • 151
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1379-1383 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The surface tensions of solutions of polyisobutylene fluids in n-heptane and tetralin have been measured at room temperature. The polyisobutylene samples studied range in molecular weight from 400 to 2800. The results conform closely to the predictions of equations previously developed from a simplified lattice theory calculation.
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  • 152
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1393-1403 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Attempts to prepare undamaged microtomed sections of crazes without reinforcement have failed. Several methods of reinforcing crazes in glassy polymers with impregnants prior to microtomy have been tried. Generalized characteristics of successful impregnant systems are suggested on the basis of this experience. The most successful system has involved the infusion of liquid sulfur into crazes in poly(2,6-dimethyl-1,4-phenylene oxide). After quenching, the solid sulfur reinforces the crazes successfully during microtomy but subsequently sublimes away under vacuum. The resultant, largely undamaged craze structure is seen by transmission electron microscopy to resemble an open-cell foam, the holes and polymer elements of which uniformly average ∼200 Å in diameter. A moderate degree of orientation in the original tensile stress direction is observed. Implications drawn from craze structure for the existence of order in the glassy state are discussed.
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  • 153
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1483-1487 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Expansion of a small spherical hole in a highly elastic solid is treated theoretically. Both elastic and surface energy terms are considered; the corresponding surface forces are assumed to be additive. The surface energy of the elastomer is assumed to be similar to that of simple liquids. Pressures or triaxial tensions required to inflate pre-existing holes to an indefinitely large size are calculated. Small holes require extremely large pressures, of the order of 1000 atm for holes of 10 Å radius. These results suggest a means of determining the distribution of hole sizes in elastomers and account in principle for experimental observations of cavitation processes. Detachment of the elastomer from a small rigid inclusion is treated in a similar way. The general absence of dilation or cavitation on stretching carbon black-filled elastomers is thus accounted for solely in terms of the small size of these filler particles.
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  • 154
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1525-1537 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The mechanical and rheo-optical properties of a styrene-butadiene-styrene block copolymer of a given chemical composition are dependent upon the morphology of the polymer as affected by the solvent system from which a polymer film is cast. Films cast from methyl ethyl ketone and from toluene are compared. Properties found to differ are the stress-strain curve, the birefringence-strain curve, stress relaxation birefringence relaxation, and the dynamic mechanical spectra.
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  • 155
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1585-1594 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A comparison is made between the experimentally obtained molecular weight distributions of nitric acid-oxidized polyethylene with a wide range of initial morphologies and the predictions of a random attack model. Deviations from the theoretical expectations are explained.
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  • 156
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1623-1626 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 157
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1721-1733 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dielectric measurements of carefully purified specimens of polystyrene and poly(2,3,4 or 3,4-chlorostyrene) have been obtained at audio frequencies ranging from 0.1 to 20 kHz and at temperatures between 4 and 300°K. Each of the samples exhibits a dielectric loss maximum in the range 15-50°K. The temperature of the maximum loss decreases with the addition of a substituent which lowers the symmetry of the pendant phenyl group. The results are explained by a model which invokes a coupling mechanism between two distinct modes of side group motions. This same model also explains some results of previously reported measurements of mechanical losses in similar polymers.
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  • 158
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1755-1760 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Rates of crystallization of polyethylene fractions have been studied at high undercoolings by differential calorimetry to demonstrate the utility of this technique for fast crystallization analysis. It has been shown that there is continuity in the crystallization kinetics from low to high undercoolings. On the other hand, the influence of molecular weight on the crystallization rates, as the undercooling increases, is very moderate, as would be expected.
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  • 159
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1577-1583 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Melting temperatures were observed visually for poly-(2,6-dimethyl-1,4-phenylene oxide) in methylene chloride at nine concentrations (polymer weight fractions ranging from 0.0042 to 0.2362). The data were analyzed upon the assumptions that ΔHu and ΔSu, the molar heat and entropy of fusion per polymer unit, are constant over the temperature range studied, and that a Flory-Huggins chemical potential expression with a concentration-independent pair interaction parameter, χ1 = (0.5 + ψ1) + ψ1Φ/T, satisfactorily describes the polymer unit activity in the binary solutions. Computation gave ΔHu = 1404 cal/mole of units (therefore Δh = 11.7 cal/g), ψ1 = -0.5691, and Φ = 342.4°K. The effect of using various combinations of data points upon the values of these three parameters, as determined by least-squares linear regression treatment of the melting temperature expression, is indicated.
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  • 160
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1595-1618 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A combination of electron-microscopy, light-scattering, and stress-birefringence studies on chemically crosslinked polyurethanes point toward the existence of rodlike regions (“bundles”), approximately 3000-8000 Å in length and involving about 5% of the volume, in which molecular orientations are correlated. The elastic behavior of these networks - as indeed that of most rubberlike networks - deviates substantially from the Gaussian behavior. The empirical representation of the data in Mooney-Rivlin plots yields C1 and C2 constants which depend on the type of imposed strain. It is thus impossible to identify C1 with the Gaussian behavior and C2 with the deviation there-from. Instead, it is found that the elastic behavior can be adequately described if it is assumed that, as a result of the bundle structure, about 5% of the segments of each chain are not free to assume the normal random-walk configurations. The determination of the number of chains in the network from the elastic behavior remains ambiguous, however, and the behavior upon swelling is not (yet) adequately reproduced by the theory. It is conceivable that in many cases deviations from Gaussian elasticity behavior may be caused by an intermolecular structuring effect, rather than by various minor deficiencies in the Gaussian model for the single chain statistics or by anisotropic excluded volume effects, as has been proposed in the past. In the present case, the amount of bundle structure, as well as the C2/C1 values, increase with the number of urethane couplings per chain, and this suggests that the interaction of the highly polar urethane couplings is responsible for the structuring. In other networks one often finds a dependence of C2/C1 on the previous history of the sample, which suggests that an accidentally trapped order may be responsible for the elastic behavior.
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  • 161
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 725-733 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The site of chain scission and crosslinking in vulcanized natural rubber irradiated with 4 MeV electrons has been determined by analysis of stress relaxation data. Sulfur and peroxide vulcanizates of different crosslink densities were prepared and the crosslink densities determined from stress-strain measurements. Stress relaxation was measured during irradiation using modified commercial relaxometers. The specimens were maintained in an atmosphere of nitrogen to minimize oxidative side effects. Scission is deduced to take place in the vicinity of crosslinks, since the rate of continuous stress relaxation is independent of crosslink density. Scission may be associated both with crosslinks initially present and with those subsequently introduced by irradiation. Crosslinking by radiation is largely a random process. However, there is a crosslinking reaction dependent to a slight extent on crosslink density as well as a small contribution from random scission reactions. G values for the random reactions are given.
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  • 162
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 743-745 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 163
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 749-749 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 164
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 763-773 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Triad tacticity data obtained by NMR analysis have previously been interpreted in terms of two basic statistical models in order to elucidate the stereospecific polymerization mechanism. In this paper the characteristics of these two basic models for stereospecific polymerization, the enantiomorphic-sites (EMS) model, and the polymer-end control (PEC) model, are examined and compared. The tacticity values accessible to the two-parameter EMS model, which includes the influence of the chain end unit, are shown to be highly restricted. Only about 20% of the isotacticity versus syndiotacticity plot is accessible to this model. To this extent the consistency of a set of triad tacticity data with the model can be tested. No such tacticity limits are exhibited by the two-parameter PEC model, which includes the influence of the penultimate unit. Any set of tacticity values which can be interpreted in terms of the two-parameter EMS model can also be interpreted in terms of the two-parameter PEC model.
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  • 165
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 809-819 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A novel gas-flow method of measuring the diffusion, solubility, and permeability of gases and vapors in polymer films is described. The specific advantages of this system over the time-lag technique are discussed. Transport data, including activation energies and enthalpies of solutions, for hydrogen and deuterium in poly(vinyl fluoride) are presented, and the effects of the glass transition and of orientation on the observed transport rates are discussed.
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  • 166
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 867-877 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: SynopsisThe diffusion of six solvents in three crosslinked, glassy epoxy polymers is studied. Case II swelling and Fickian sorption are observed as two simple limiting cases. The mechanism of diffusion changes from one limit to another as the nature of the solvent or the crosslink density of the polymer is altered. With mixed solvents, properly chosen, a superposition of Fickian diffusion and case II swelling is observed.
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  • 167
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 897-907 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly-ε-caprolactone prepared by a dibutylzinc-catalyzed bulk polymerization process was fractionated, and the solution properties of the fractions were studied in benzene and in dimethylformamide. In these solvents at 30°C the Mark-Houwink relations were [η] = 9.94 × 10-5 Mw0.82 and [η] = 1.91 × 10-4 Mw0.73, respectively. The value of KΘ was found to vary from 1.1 to 1.2 × 10-3 when determined by three known extrapolation techniques. Poly-ε-caprolactone chains appear to be quite flexible in solution, and the steric hindrance parameter σ had the low value of 1.37. Root-mean-square end-to-end dimensions were approximated from the experimental data and calculated from the Debye-Bueche and the Kirkwood-Riseman theories.
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  • 168
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 983-992 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Interferometric studies have been made on cotton fibers as well as on twisted nylon filaments. The results so obtained provide strong evidence that the fibrils in the cotton fiber become less inclined to the fiber axis as one proceeds from the surface to the core. Also, studies on twisted nylon filaments by the fiber refractometer and Becke line techniques indicate that the latter, as practiced in this laboratory, does give values of refractive index which are heavily weighted towards the fiber periphery.
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  • 169
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1005-1019 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements of T1ρ as a function of temperature have been made on three polyethylene oxides (PEO) with molecular weights of 550, 6000, and 2.8 × 106 in order to try to elucidate various problems arising in the interpretation of previous T1 measurements on PEO. In contrast to the T1 measurements, the T1ρ measurements show discontinuities at the melting or softening points of the respective polymers concerned, and also show nonexponential magnetization decay in the case of PEO 6000 and 2.8 × 106, which is presumbly due to the existence of “mobile” and “crystalline” regions, in qualitative agreement with NMR studies and x-ray measurements. Motional correlation frequencies and activation energies have been derived where possible by using the BPP theory adapted to the rotating frame and also the strong collision Slichter-Ailion theory. There is reasonable correlation with other data on motional frequencies where it is available, although the overall situation for the so-called α transition in PEO 6000 and 2.8 × 106 is still not clear. It is suggested that spin-diffusion is an important mechanism for all three polymers; for PEO 550 because it contains CH3 endgroups which act as sinks, and for the other two polymers where the mobile fraction performs the same function.
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  • 170
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1085-1099 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements of infrared absorbance as a function of temperature down to 77°K have been made on poly(ethylene terephthalate). Transitions observed by other techniques such as torsion pendulum measurements are reflected in the infrared measurements by an abrupt change in the slope of the absorbance versus temperature. The infrared measurements are made on bands of known structural origin so the structures contributing to each transition can be determined. The β transition is shown by infrared to be a composite of two peaks with the lower-temperature portion arising from the amorphous regions and the higher-temperature portion from the crystalline regions.
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  • 171
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1119-1121 
    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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  • 172
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1123-1150 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Stress, strain, and birefringence measurements have been carried out on swollen and unswollen networks of ′cis-1,4-polybutadiene polymers. Neither stress-strain nor birefringence-strain relations of unswollen specimens obey the Gaussian network theory, but both can be fitted by the Mooney-Rivlin equation. On the contrary, data on specimens swollen in tetralin, decalin, benzene, and carbon tetrachloride strictly obey the Gaussian network theory. Existing methods for evaluating the temperature coefficient of the unperturbed dimensions, d In 〈r2〉/dT, from the stress-temperature relation are applied to the present data and discussed in some detail. It is concluded that reliable values of d In 〈r2〉/dT are not obtainable from data on unswollen samples because of the pronounced non-Gaussian effect. The value 7.5 Å3 for the optical anisotropy Å3 (an alternative to the stress-optical coefficient) for unswollen specimens is markedly larger than values (5.8 Å3 on the average) for swollen specimens. This is interpreted as due to the shortrange orientational order among polymer segments. The quantities 〈r2〉, ΔΓ, and their temperature coefficients are calculated for both cis-1,4-polybutadiene and cis-1,4-polyisoprene chains, on the basis of the rotational isomeric state approximation for bond rotations. Values of ΔΓ for cis-1,4-polybutadiene calculated using Clément and Bothorel's set of anisotropic bond polarizabilities are in good agreement with observed values for swollen specimens. Those for cis-1,4-polyisoprene obtained using the same set of anisotropic bond polarizabilities are somewhat smaller than observed values for unswollen specimens. This departure is in the direction expected from the behavior of ΔΓ upon swelling (i.e., a decrease in ΔΓ upon swelling).
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  • 173
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1405-1414 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Molecular motions in poly(vinylidene fluoride) were studied by the dielectric technique. Three distinct absorption peaks (αc, αa, and β) were observed in the frequency range from 0.1 cps to 300 kcps and in the temperature range from -66 to 100°C. The molecular mechanisms for these absorptions and their temperature dependence are discussed, and results are compared with x-ray diffraction and the NMR measurements. It is concluded that the αc absorption located at 97°C (1 kcps) is related to molecular motion in the crystalline region. The αa absorption located at -27°C (1 kcps) can be interpreted as due to the micro-Brownian motion of the amorphous main chains. The β absorption located at -47°C (1 kcps) is attributed to local oscillation of the frozen main chains.
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  • 174
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1444-1449 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 175
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1559-1575 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dielectric constant and dielectric loss of copolymers of methyl methacrylate (MMA) with n-butyl methacrylate (nBMA) and isobutyl methacrylate (iBMA) have been measured in the frequency range 30 cps to 1 Mcps at temperatures from 70°K to 370°K. Results lead, together with those of previously published investigations on copolymers of MMA, to the following conclusions. (1) The loss-peak temperature attributed to side-chain relaxation (β peak) of PMMA varies with the comonomer ratio when the comonomer does not have an α-methyl group, but remains almost unchanged for comonomers having an α-methyl group. (2) In both cases, the β peak height of PMMA decreases with increasing ratio of comonomer B and completely vanishes for poly-B, and the loss peak temperature plotted against the fraction of B does not extrapolate to the β peak of poly-B. It is suggested on the basis of the above facts that the moving unit in the side-chain relaxation consists of a single side chain with a segment of the backbone chain and that the change in mobility of the side chain upon copolymerization results from the distortion of the helical structure of the backbone chain due to random distribution of α-methyl groups. Dielectric studies of the low-temperature side-chain relaxation (β2 peak) in PnBMA, poly(n-octyl methacrylate), and poly(n-dodecyl methacrylate) (130°K at 1 kcps) have been made and an interpretation is offered for the molecular nature of this relaxation.
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  • 176
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 27-36 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Silica flocculated with a high molecular weight poly(DMVPMS) contains aggregates that are stable enough to permit size measurement with a Coulter counter. The average size of these aggregates increases up to a critical level of added polymer; the primary particles reappear at higher levels of added polymer. The aggregate size is reduced by continued mixing and the particle size distribution before flocculation is approached. Subsidence rates, equilibrium sediment volumes, and refiltration rates give somewhat different estimates of the degree of flocculation. Additional aggregation beyond that measured by the Coulter counter must be considered in the interpretation of these data. The decrease in floc strength during continued agitation is attributed to a disaggregation of the bridging polymer, to a decrease in the interparticle bonding of the bridging polymer, and to an increase in the surface coverage with polymer.
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  • 177
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 77-86 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The random depolymerization model of Montroll and Simha for originally homogeneous polymers is derived analytically by utilizing a weight distribution function approach not requiring the use of any approximations. The model is then extended to consider heterogeneous initial chains having an arbitrary chain length distribution. The probabilities for breakage are assumed to be identical for all bonds joining monomeric elements in the system and to be independent of chain length and position in the chain, assumptions also used in the model of Montroll and Simha. An expression is found for estimating the probability of bond breakage.
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  • 178
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 113-122 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Differences in structural parameters, shrinkage, and retractive forces have been compared for nylon 66 tire yarns annealed at several temperatures in silicone oil and in air. It is found that significantly different structural changes occur for oil-annealing and air-annealing. Retractive forces measured in hot oil are characterized by a high initial force, followed by a rapid decay and a second, more gradual, increase which is also followed by a decay at sufficiently high temperatures. In heated air, the first, short-term, retractive force is absent. It is postulated that these differences are due to the different rates of heat transfer at gas-solid and at liquid-solid interfaces, and that rapid heat transfer (as in the case of oil-annealing) promotes two mechanisms of molecular change which are characterized by different degrees of structural parameter change, and by different amounts of shrinkage.
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  • 179
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 163-170 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A resolution index for gel-permeation chromatograph (GPC) columns is defined by the relation log (RI) = αW, where RI is the resolution index, α is the slope of the calibration curve of logarithm of molecular weight against peak position for narrow polymer fractions, and W is the width of the GPC curves for narrow fractions. This resolution index is calculated approximately for several GPC columns individually and in series combinations by using data obtained on narrow fractions of polystyrene. The index increases with number of columns and with flow rate over a limited range of flow rate, does not vary much with solvent, and does not correlate well with plate count obtained with low molecular weight molecules. It is believed that the resolution index provides an improved indication of the performance of GPC columns.
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  • 180
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 219-229 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The compressibility of polyisobutylene and polystyrene above their glass transition temperature is treated as the sum of two parts; a free-volume compressibility and, as originally suggested by Bridgman, a compressibility of the molecules themselves. Two different models are used to treat the free-volume compressibility, and as a result values for the molecular compressibility are estimated. These are in reasonable agreement with other values in the literature. The magnitude of this “molecular compressibility” is then considered in relation to some existing treatments of intermolecular forces. These suggest that intermolecular contacts are more compressible than covalent bonds, and on this basis the observed levels of molecular compressibility can be explained.
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 297-307 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The molecular weight distributions of three polydimethylsiloxanes (PDMS) have been determined by gel-permeation chromatography (GPC), by gas-liquid chromatography (GLC), and by precipitation fractionation. The GPC data are greatly improved by correction for band spreading. For a high molecular weight polymer the corrected distribution agrees closely with the theoretical molecular weight distribution calculated from polymerization kinetics.
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  • 182
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 357-375 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The assumed analogy between polymer solutions and polymer-network gels as regards the thermodynamics of swelling - a fundamental assumption implicit in all previous analyses of swelling measurements on gels, aimed at checking the statistical theories of rubber elasticity - is shown in fact to be rather limited. In particular, excluded volume effects, which play a dominant role in both solutions and gels, are quite different in the two types of systems. A new thermodynamic description of swelling equilibria, taking account of differences in excluded volume effects, is given, and analogies and differences between gels and solutions are pointed out.
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  • 183
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 405-410 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Multiphonon contributions to the directional phonon frequency functions are calculated for crystalline polyethylene. These results are compared to previously calculated one-phonon frequency functions.
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  • 184
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 429-429 
    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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  • 185
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 515-524 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An x-ray study of poly(N-butyl isocyanate) (PBIC) was undertaken with the aim of providing the structural information required for the calculation of its ultraviolet absorption spectrum. Well defined diffraction patterns are obtained from powder samples and oriented films of the polymer cast from cyclohexane solution. All the reflections can be satisfactorily indexed in terms of a pseudo-hexagonal unit cell with a = 13.3 Å and c = 15.4 Å. This indexing and the intensity distribution lead to the conclusion that PBIC has a helical structure with a translation of 1.94 Å and a rotation of 135° per monomeric unit (i.e., the c axis corresponds to 8 units in 3 helical turns). In the absence of single-crystal data on closely similar model compounds, a range of possible bond lengths and angles was assumed. The atomic coordinates of the chromophoric group of PBIC were then computed using the restrictions imposed by the helical parameters. From an investigation of all the assumed range of bond lengths and angles, a few closely similar structures having no unacceptably short van der Waals contacts were found. A comparison of calculated and measured densities indicates that there are two molecules per unit cell. Construction of space-filling models of PBIC supports this conclusion.
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  • 186
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 563-574 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Solution parameters for the polymer poly-γ-trifluoro-propylmethylsiloxamer has been determined in cyclohexyl acetate, methyl hexanoate, and ethyl acetate. Interpretation of data follows the theory of Fox and Flory. In contrast to poly-dimethylsiloxane, an increased steric hindrance to rotation about the siloxane bond occurs as evidenced by the characteristic ratio of root-mean-square end to end dimensions, (r02/r0f2)1/2, found to be 1.90 and 1.96 at 25.0 and 72.8°C, respectively. This increase is considered to be primarily due to nearest-neighbor interaction of the polar substituent on the silicon atom. The relation, [η]θ ∝ M1/2, was observed to hold for this polymer system. The hydrodynamic model appropriate for the polymer is a random coil considerably more permeable to solvent flow than is generally reported for linear polymers. The universal parameter φ was determined to be 1.5 × 1021. The effect of temperature on polymer configuration is indicated to be negligible.
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  • 187
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1281-1282 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
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  • 188
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1357-1366 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Three types of commercial styrene-acrylonitrile copolymer were fractionated by coacervate extraction and by column-elution techniques. Both methods were studied with two different solvent-nonsolvent pairs. Glass wool was used as the support material in the column. Fractionation by the coacervate extraction method was studied with benzene-triethylene glycol as a solvent-nonsolvent system at 60°C and with dichloromethane-triethylene glycol at 25°C. Column elution was carried out with acetone-methanol as the solvent-nonsolvent system at 30°C, and with dichloromethane-methanol at 20°C. Results of excellent reproducibility were obtained by these two methods. Characterization of fractions involved determination of both the molecular weight and chemical composition. It was established that the fractionation of the samples tested was dependent upon molecular weight only. The two methods described above are compared. Each gives an efficient procedure for fractionation of styrene-acrylonitrile copolymers.
    Additional Material: 6 Ill.
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  • 189
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1451-1459 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The adiabatic compressibility for two samples (F-1 with DP-3748 and F-2 with DP-2114) of poly(4-vinyl-N-n-butylpyridinium bromide) in aqueous solution has been determined from ultrasonic velocity and density data. The sample (F-1) with the higher degree of polymerization shows comparatively higher velocity and density in solution. However, the evidence for the difference in compressibility is not very decisive. The apparent molal volume ΦV2 and apparent molal compressibility ΦK2 for F-1 are found to be slightly higher than for F-2. In aqueous solution, the decrement of adiabatic compressibility per unit concentration, (β1 - β)/c, is found to be almost constant throughout the entire concentration range, whereas in the presence of excess added electrolyte (1.0M KBr solution), the compressibility decrement shows a decrease with dilution. The latter values are lower than those found in water, since the molecules, in the presence of excess electrolyte, are coiled up more and are less compressible. The ΦV2 and ΦK2 values in water are constant throughout the entire concentration range, as the free counterions formed on dissociation in the dilute region are not solvated and hence contribute little to the compressibility. On the other hand, in the presence of excess KBr (1.0M), the ΦV2 and ΦK2 values show a sharp decrease with increase of polyelectrolyte concentration and finally attain a constant value. This is explained by the fact that because of the formation of a charge-transfer complex between the bromide ion and the polycation, more than the equivalent number of bromide ions is bound, leaving free an equal amount of K+ ions which are solvated and cause the lowering of apparent volumes and compressibilities. Condensation of charges begins at a certain polyelectrolyte concentration, and no further increase of K+ ions is observed. A special situation arises in 0.1M KBr solution. The ΦV2 and ΦK2 values at first increase sharply with increase of polyelectrolyte concentration, but then level off to attain a constant value, at comparatively high concentration. In 2.0% poly(4-vinyl-N-n-butylpyridinium bromide) solution, the concentration of polymer repeat unit (0.08M) is almost equal to the concentration of the added electrolyte (0.1M KBr) used to suppress dissociation. As the polyelectrolyte concentration in 0.1M KBr solution is progressively decreased, more bromide ions are made available for forming the charge-transfer complex with the polycation, leaving the K+ ions free to contribute to the compressibility.
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  • 190
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1495-1511 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements are reported of the vapor pressures and the heats and volumes of mixing of solutions of poly(ethylene glycol dimethyl ether) in chloroform and in carbon tetrachloride. The measurements have been used to calculate the thermodynamic mixing functions for mixing with zero volume change. These values have been compared with the predictions of the lattice theory of mixtures at three different levels of approximation, viz., the generalized “first approximation” theory of Barker, the “zeroth approximation” theory, and the Flory theory. In the hydrogen-bonding chloroform solutions the Barker theory is more successful than the other forms of the lattice theory. The results have also been used, in conjunction with those for solutions of poly(propylene glycol dimethyl ether) in the same two solvents, to test the ability of the Barker theory to correlate the properties of related systems. Good correlation is found between the two carbon tetrachloride solutions but not between the chloroform solutions. It is probable that the side-chain methyl groups in the propylene oxide repeating unit cause the hydrogen-bonding interaction to be weaker in this polymer than it is in the polymer with the ethylene oxide repeating unit.
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  • 191
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1627-1638 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new type of long-range interaction between chain segments and solvent molecules in a polymer molecule is introduced. It can be depicted as an “interfacial” free energy, due to the more or less diffuse interface between the interior of a polymer coil and the surrounding solvent. Flory's calculation of the coil expansion α is extended for this effect, by using theoretical approaches developed by van der Waals, Cahn and Hilliard, and Debye for inhomogeneous systems (interfaces). It is found that Flory's equation for α is replaced by: \documentclass{article}\pagestyle{empty}\begin{document}$ \alpha ^5 - \alpha ^3 = 2C_M \psi _1 M^{1/2} \left[ {1 - \left( {\theta /T} \right) + \left( {15/2\alpha ^2 } \right)\left( {\theta /T} \right)\left( {l^2 /\overline {r_0^2 } } \right)} \right] $\end{document} where the last term is due to the “interfacial” free-energy correction. The Debye molecular interaction length l is also found in theories on light scattering of binary mixtures near the critical solution temperature. An important result of this equation is that at T = θ, α is not equal to unity, as before, but somewhat larger, depending on the molar mass of the polymer and the solvent type. A calculation shows that the “interfacial” free energy correction may contribute substantially to the “solvent” effects on the expansion of a polymer molecule at the θ temperature, as has recently been reported in the literature.
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  • 192
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1695-1704 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Hv cloverleaf scattering pattern sometimes found for amorphous polymers can arise from the birefringent region caused by the strain surrounding a void or an inclusion in a polymer. The form of such a pattern may be theoretically explained by extension of a theory due to Goldstein.
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  • 193
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 257-270 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The orientation of crystallites grown isothermally in several drawn trans-polychloroprene networks is studied as a function of crystallization temperature tx, degree of crystallinity ω, and elongation ratio α. The orientation distribution is particularly simple for this polymer since the crystallographic c axis (chain axis) orients preferentially along the stretching direction, while a and b are randomly arranged about c. Hence the parameter cos2 χc adequately characterizes the distribution, where χc is the angle between the c axis and the fiber axis, and the average is taken over all crystallites. A treatment due to Krigbaum and Roe is utilized to obtain values of v (the number of statistical segments comprising the crystallization nucleus of critical size) through comparison of the average orientation of crystallites and amorphous statistical segments. The behavior observed falls into two categories. First, if the initial amorphous network is well oriented, 〈cos2 χc〉 is independent of crystallinity during both crystallization and melting, and v varies with tz (or the degree of supercooling) as predicted by nucleation theory. If different networks are to have the same crystallite orientation distribution, they must not only be crystallized at the same supercooling, but must also have the same distribution of amorphous segment orientations. Both the relative elongation and the network crosslink density affect the latter distribution. Next, we consider the second category. If the initial amorphous orientation is poor, 〈cos2 χc〉 decreases linearly during crystallization and increases along approximately the same path during melting. Further, 〈cos2 χc〉 for a given tz yields v values which are too large. These two behaviors can be explained if, in the former case, nucleation involves the best oriented statistical segments of all network chains, while in the latter there is a selection according to the chain displacement vector orientation. Thus, if the amorphous orientation is poor, both the orientation and thermodynamic stability of the crystallites decreases with further crystallization. If this decreased stability is reflected in shorter fold lengths, the reversible variation of long period spacing with temperature reported earlier for an oriented polychloroprene network can also be explained as a preferential melting process.
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  • 194
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 377-388 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The design of a differential thermal analysis apparatus for use at elevated pressure is described. Experiments on melting and crystallization of folded-chain crystals of polyethylene and poly(ethylene-butene-1) copolymer, and melting of extended-chain polyethylene crystals have been conducted at pressures up to 4200 bars. The precision in transition temperature measurement was ±1°C. The Clausius-Clapeyron equation predicts the melting point increase with pressure at atmospheric pressure to be 32.0°C/kb. The melting point depression due to copolymerization remained constant over the complete pressure range analyzed on the poly(ethylene-butene-1) used in this study. Crystallization of polyethylene is retarded at elevated pressures, and a 50% larger degree of supercooling is necessary at 5000 bars to give a crystallization rate equal to that observed at atmospheric pressure. The difference in melting point between folded-chain and extended-chain polyethylene increases from 8.4°C at 1 bar to 25.6°C at 3000 bars.
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  • 195
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 423-424 
    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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  • 196
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 431-431 
    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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  • 197
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 201-208 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polymer crystals are characterized by strong anisotropy of binding forces among units, i.e., the intrachain force constant f is much larger than the interchain force constant g. The anisotropic lattice is reduced to an isotropic one, in which each lattice point represents N* units (segment) along the chain axis of the anisotropic lattice [N = 2(f/g)1/2]. Vibrational modes of the reduced lattice correspond to interchain modes of the original lattice, i.e., modes whose frequencies are governed by interchain potential. Anharmonicity of crystalline force field is assumed to be related predominantly with interchain force alone. Thermodynamic and transport equations for a simple lattice are applied to the reduced, isotropic lattice, and numerical results are obtained for high-density polyethylene. The Grüneisen constant γ was obtained from the pressure dependence of sound velocity. The heat capacity of the reduced lattice, Cinter (interchain specific heat), was calculated from Grüneisen's equation, α = γβCinter (where α = thermal expansion coefficient, β = compressibility), and the mass of a segment m* was estimated from Dulong-Petit's equation, Cinter = 3ρk/m* (where ρ = density, k = Boltzmann constant). The value of m* is consistent with N* from force constants, m* = N*m (where m = mass of a unit in the original lattice). m*θ3 (where θ denotes the Debye temperature of the reduced lattice) is calculated from low temperature specific heat. The value of m* calculated from m*θ3 and θ from other sources agrees with that from the estimate by Dulong-Petit's equation. The high-temperature thermal conductivity K was calculated through Leibfried-Schloemann's equation by employing γ and m*θ3 as estimated as described above; satisfactory agreement was obtained with experiment. Poly(methyl methacrylate) and polystyrene were also studied by similar methods.
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  • 198
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 253-254 
    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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  • 199
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    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 309-324 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Huggins and Kraemer equations generally used to determine intrinsic viscosity frequently do not yield identical results, and their constants often do not add up to 1/2 as is mathematically required. To overcome these difficulties an equation has been deduced which through linear plots gives unambiguous intrinsic viscosities, constants which meet the 1/2 condition, as well as two other flow constants. Extensive tests of the equation with precise data on solutions of poly(methyl methacrylates) and polystyrenes in benzene and toluene confirm the validity of the new equation in every respect. It is further shown that the four constants involved are interrelated, and that it is possible to express the values of three of these in terms of the fourth.
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  • 200
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The mechanical anisotropy of regenerated cellulose films is investigated, first, on the basis of the theory of infinitesimal elasticity. Fairly good agreement of calculated with observed results is obtained on the basis of orthogonal anisotropy with respect to the machine direction and the transverse and thickness directions of the films. The shear modulus G23 along the film plane and the Poisson ratio v32 are 1.5 times; 102 kg/mm2 and about 0.4, respectively, in the standard dry state. Second, the mechanical anisotropy in three different dry states is analyzed in terms of the degree of biaxial orientation of two kinds of structural units, cellulose II crystallites and noncrystalline chain segments, and their mechanical anisotropy. The calculation for averaging the mechanical anisotropies of these structural units on the basis of the homogeneous strain hypothesis gives results much higher than the experimental data, whereas the calculation on the basis on the homogeneous stress hypothesis gives results rather lower than experiment. As a modification of the two extreme calculations, a different averaging gives considerably better agreement between the calculated and observed results. The mechanical anisotropy in the wet state is further analyzed primarily in terms of the degree of biaxial orientation of noncrystalline chains by a modification of Krigbaum treatment, based on application of the kinetic theory of entropy elasticity for semicrystalline polymers, to anisotropic systems. The calculation gives results, however, much lower than those obtained experimentally, unless the ratio of the end-to-end distance of the noncrystalline chain to its fully stretched length is taken as unusually large. This may be due to underestimation of the contribution of the crystalline phase to terms of the same type as appear in the Krigbaum treatment.
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