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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 939-949 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(N-ethyl laurolactam) and poly(N-benzyl laurolactam) were prepared from the corresponding monomers by hydrolyic polymerization. Unlike the partially crystalline poly(N-methyl laurolactam), these two homopolymers were completely amorphous by x-ray diffraction. Diffraction patterns of copolymers of N-ethyl laurolactam or N-benzyl laurolactam with laurolactam were shown to be composition-dependent. For N-ethyl laurolactam copolymers, crystallinity developed with 20% laurolactam as a comonomer and increased steadily with a subsequent change in the x-ray pattern, up to 50% laurolactam. Higher laurolactam percentages resulted in copolymers having a nylon 12 x-ray pattern. N-Benzyl laurolactam copolymers with 30% laurolactam showed only 6% crystallinity. The x-ray patterns of N-benzylated nylon 12 made with more than 50% laurolactam showed patterns similar to that of nylon 12. Differential scanning calorimetry data of all these polymers substantiate the x-ray findings. The effect of type and concentration of the N-substituent on the glass transition, melting, and crystallization temperatures of the polymers is discussed.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1077-1089 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystal structure of nylon 12 prepared by polymerization of dodecalactam has been determined by x-ray diffraction. Nylon 12 fiber exhibits only the γ form as its stable crystal structure. The unit cell of nylon 12 was determined with the aid of the x-ray diffraction pattern of a doubly oriented specimen. The unit cell is monoclinic with a = 9.38 Å, b = 32.2 Å (fiber axis), c = 4.87 Å and β = 121.5° and contains four repeating monomer units. The chain is planar zigzag for the most part but is twisted at the position of amide groups, forming hydrogen bonds between neighboring parallel chains. The chain conformation is similar to that of the γ form of nylon 6 proposed by Arimoto. It was deduced from the calculations that there are two chain conformations statistically coexistent according to the direction of twisting. In each conformation, hydrogen bonds are formed between parallel chains to make pleated sheetlike structures. The sheets are nearly parallel to (200) and in the sheet the directions of the neighboring chains are antiparallel, as is the case with nylon 6.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1091-1109 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Three different polyolefins, a linear polyethylene, an isotactic polypropylene, and an isotactic polybutene-1, were melt-spun into filaments. The degree of orientation of the filaments was measured by polarized-light microscopy, x-ray diffraction, and a retraction technique, and the results were then related to the melt-draw ratio. The increase in the elastic deformation ratio of polymer chains by spin-stretching, estimated by thermal retraction at a temperature above Tm, was monotonic with respect to the melt-draw ratio. On the other hand, as-spun filaments of polyethylene and polypropylene were characterized by a plateau in birefringence over the range of melt-draw ratios from 8 to 80. The change in orientation functions for crystals in these filaments was similar to the change of birefringence. On the other hand, the birefringence and the crystalline orientation functions for polybutene-1 increased smoothly with increasing melt-draw ratio. The most highly melt-drawn filaments of these polymers had a strongly oriented structure, corresponding to that in highly cold-drawn specimens.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1117-1138 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An attempt to interpret the prominent dielectric relaxations of poly(γ-benzyl L-glutamate) and poly(γ-methyl L-glutamate) in terms of their structures was made by applying the barrier theory of Hoffman. Potential energy maps for the rotation of the polar side group, which are required in this application, were calculated by taking account of molecular environment of the polar side group. The dichroic ratios from infrared measurements were satisfactorily calculated, based on the maps. This provides evidence that the maps are reliable. In applying the barrier theory, it was modified by the assumption that the conformations of the side groups are distributed according to the Boltzmann law. On the basis of the maps, the magnitude of the dielectric absorption and the mean relaxation time were calculated in terms of the modified barrier theory; these were in fairly good agreement with the experimental data.
    Additional Material: 15 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1247-1249 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1301-1318 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Heat capacity values for melts of polystyrene, poly(methyl methacrylate), polypropylene, and polyethylene are calculated on the assumption that the total constant-volume heat capacity Cv is made up of two parts: one associated with molecular vibrations, and one, with holes. Numerical values of both components are given for a wide range of temperatures and compared with experimental data. For poly-1-butene insufficient data for complete evaluation are available, so that only the vibrational contribution could be discussed.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1319-1330 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The resistivity and dielectric constant for carbon black (5-12 vol-%) in a nonconducting matrix have been measured over the range 20-90°C and dc to 2-105 Hz. Styrene-butadiene rubber dissolved in tetracosane (22 parts SBR to about 70 parts wax) constituted the matrix. Wide variations in resistivity and dielectric constant with temperature and/or frequency were observed. A theory is presented to explain the experimental observations. It correctly predicts the qualitative features of the experimental results but its predictions are not quantitatively accurate.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1293-1300 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: There have been several investigations dealing with the influence of the glass transition on the rate of radiation-induced reactions, especially the crosslinking reaction. On the other hand, no correlation has been reported between secondary transitions and the variation of a reaction rate. In the present work, the degradation of poly(methyl methacrylate) in the temperature range of -196 to 160°C has been studied. Two breaks in the Arrhenius plot were found. The first one is located at -5°C and can be correlated with the γ transition, which has been assigned to the hindered rotation of the ester group whose scission initiates the degradation. It is concluded that the thermal excitation of the bond rotation can either increase the scission rate or decrease the recombination rate of reactive intermediates by expanding the cage of the surrounding molecules. If the second mechanism occurs, the rotation of the α-methyl group should also be expected to favor the degradation. However, a second break in the Arrhenius plot was found at -130°C, and therefore significantly above the δ transition. The influence of this motion is therefore not clear. Certain radiation-induced reactions of poly(vinyl chloride), known from literature, seem to be influenced by a secondary transition. It is concluded that secondary transitions may be significant for scission reactions. This suggests, with respect to the known significance of the glass transition, that the various types of molecular motions in polymers may influence radiation-induced reactions.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1347-1355 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dynamic light-scattering experiments were performed on an ethylene-methacrylic acid copolymer and its sodium salt. The in-phase ΔI′ and out-of-phase ΔI″ components of the light scattering were measured in a temperature range between 25 and 65°C for both samples. No transition is seen in this temperature interval for the acid, but a clear transition occurs around 40°C for the salt. This transition is associated with the softening point of the ionic domains present in the sample.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1357-1374 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A general equation describing the small-angle Hv light-scattering intensity for a system of N undeformed spherulites located at random within the sample and taking into account the truncation and interference effects is given. Scattering contour plots or radial scans are reported for various arrangements of the N spherulites. The results show that the interference effect may explain the speckled appearance of the experimental patterns. Moreover, the interference and truncation effects (for the special cases where truncation is considered here) do not seem to shift the position of the maximum scattering angle of the cloverleaf pattern as calculated from the single spherulite theory. Finally, the calculations show that the truncation effect increases the relative intensity of the pattern at large and low scattering angles and at azimuthal angles 0 and 90°C, as compared with the intensity at the position of maximum scattering angle.
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  • 11
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1555-1572 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Sorption, diffusion, swelling, and tensile stress relaxation measurements were made at room temperature (23°C) for the systems poly(n-butyl methacrylate) (PBMA) with liquid methanol and ethanol, and poly(methyl acrylate) (PMA) with liquid water. Stress relaxation curves for the fully swollen polymers could be superimposed approximately with those for the dry polymers by appropriate shifting along the long axes. For PMA-water the measured curve for stress relaxation with concurrent sorption could be predicted accurately by using a moving boundary theory with data measurements of stress relaxation of the unswollen and swollen polymer combined with sorption data. The modified moving boundary theory is generalized to include the effects of dimension changes through swelling and the larger effects of plasticization associated with sorption of liquids. This improved theory accurately predicts measured curves of stress relaxation with concurrent sorption for the PBMA-alcohol systems from individual stress relaxation, sorption, diffusion and swelling data. The general approach should be applicable to other amorphous polymer-liquid swelling agent systems. The anisotropic nature of swelling of polymer films and its effect on calculated diffusion coefficients are discussed briefly.
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  • 12
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1747-1758 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The basis for obtaining the steady-state compliance from stress relaxation upon cessation of steady flow (SRUCSF) data is derived. Measurements on three polymer solutions of differing molecular weight, polydispersity, and degree of entanglement coupling show good agreement between results from SRUCSF and creep-recovery experiments in both linear and nonlinear viscoelastic regions. The stress overshoot phenomenon is interpreted in terms of a change in entanglement spacing upon imposition of a shearing field. The phenomenon is analyzed in terms of a relaxation time for re-entanglement, which is found to be much longer than the relaxation time of the shear stress upon cessation of steady flow.
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  • 13
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1779-1791 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The morphological character of uniaxially oriented poly(ethylene terephthalate) (PET) films was investigated as a function of draw ratio. Dynamic mechanical, infrared, and crystallite-size measurements were made on the samples. In addition, selective degradation experiments and molecular weight determinations were employed. The dynamic mechanical measurements indicated a sharp decrease in irregular folds for draw ratios of 3.0 and higher, which also coincided with the essentially complete disappearence of regular folds (from the 988 cm-1 band in the infrared spectra) in unannealed samples. Infrared studies of drawn samples annealed under different conditions gave evidence in support of a structure in which the chains are stretched out. Apparent crystallite-size measurements showed a sudden increase in length of the crystals in the direction of the draw beyond a draw ratio of 3.0. Molecular weight measurements showed a large increase in average chain length in the residue after selective degradation of amorphous material and folds; undrawn and slightly drawn samples gave a much lower Mn. Based on these observations, it is postulated that for higher draw ratios and present drawing conditions, the crystals are of the straight chain type, somewhat similar to the fringed-micelle crystal concept.
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  • 14
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1817-1828 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The heat capacity of polyhexene-1 was measured between 20 and 300°K. The apparatus, an adiabatic calorimeter giving results with a random error of 0.2-0.4%, is briefly described. The characterization of the sample by x-ray diffraction patterns established that it was amorphous at all temperatures. Gold foil was incorporated with the sample to increase the apparent thermal diffusivity and so to decrease the time needed for the measurements. The glass transition temperature was found to be 215.5 ± 1°K. On the Cp curve, no subglass anomaly was detected, unlike the results of experiments described elsewhere. The calculation of Cv is discussed, and an explanation is given for the choice of the number of intramolecular vibrational modes per monomer which are assumed to contribute to Cv. A linear continuum model with characteristic temperature θ1 = 736°K allows us to fit the experimental curve over a temperature range of 140°K.
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  • 15
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1849-1854 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 5 Ill.
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  • 16
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1863-1864 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 17
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1949-1961 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Cast samples of a phenol-formaldehyde polymer with a crack of length defined by a metallic foil inclusion were fractured in tension. The stress at fracture was inversely proportional to the square root of the crack length, in agreement with the Griffith equation for brittle fracture. The behavior did not conform to the Griffith equation with respect to the experimental value of surface free energy, which was several orders of magnitude higher than a theoretically calculated value. However, as the temperature of tensile testing was raised, the experimental value did approach the calculated value. Consistently the appearance of the fracture surface was observed to change from one showing evidence of plastic deformation at room temperature to a featureless appearance, characteristic of brittle fracture, at higher temperatures.
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  • 18
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2013-2026 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: By the differential operator representation of constitutive equations for linearly viscoelastic materials, general theoretical expressions are developed for the physical parameters of a composite system in relation to those of the constituents. The interfacial tension between the dispersed phase and continuous matrix is included in the derivation. The results show that it has effect only on the shear parameter but not on the bulk parameter of the composite system. The general expressions developed in this article represent a unified theory for composite systems. The results are shown to reduce to many special cases obtained by other investigators.
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  • 19
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2079-2088 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The glass transition in styrene-based ionomers was investigated by means of infrared spectroscopy and differential scanning calorimetry (DSC). Transition temperatures were determined from the temperature dependence of the peak absorbances of the 1700 and 1745 cm-1 bands. These transition temperatures agreed with glass transition temperatures (Tg) determined by DSC. With increasing degree of ionization, Tg and the enthalpy ΔH of the residual intermolecular hydrogen bonding increased. The values of Tg obtained were analyzed by the theory of Fox and Loshaek for the effect of crosslinks. It is concluded that sodium ions probably from ionic domains and act as crosslinks to reinforce the residual hydrogen bonding and may increase Tg. The absorbance at 1560 cm-1 (νCOO-) did not change at Tg. This suggests that the glass transition observed here is not due to the onset of the mobility in ionic domains, as has been proposed for ethylene-based ionomers on the basis of dielectric measurements.
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  • 20
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2123-2133 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements of apparent viscosity, normal stress coefficient, and storage and loss moduli have been used to determine the characteristic relaxation time. The ratio of the characteristic relaxation time θin corresponding to a given deformation rate ·γ to that of the initial state θe is found to be a function of ·γθin. For a wide range of polymeric systems, the ratio of normal stress to the initial high elasticity modulus and to the high elastic deformation γe are the same function of ·γθin. It has been established that γe, like other viscoelastic characteristics of polymer systems, is determined by the relaxation properties and their variation due to deformation. The dependence of γe on θe/θin is common to a wide range of polymeric systems. The generalized characteristics were independent of the nature of the polymeric chain, molecular weight, molecular weight distribution, temperature, polymer concentration in solution, and solvent type. These results allow us to describe approximately normal stresses and high-elastic deformations as functions of shear rate and storage and loss moduli as functions of frequency, if we know θin the relation between shearing stress and shear rate.
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  • 21
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2185-2197 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of energy calculations have been carried out in order to describe the epitaxial crystallization of polyethylene from solution in terms of molecular interactions. The total energy has been computed as the sum of electrostatic, dispersion, and repulsion contributions. The potential energy associated with a section of a planar-zigzag polyethylene chain has been determined for various orientations and positions above three different planar alkali halide substrates. Inspection of the energy surfaces as a function of the spatial degrees of freedom reveals that the minimum energy orientation of the chain is that for which it is parallel to the substrate [(001) cleavage plane] and aligned in the 〈110〉 direction on the surface, a result in accordance with available experimental evidence. Specifically, the chain preference is to position itself along rows of positive ions, whereas alignment along rows of negative charge appears energetically unfavorable. The mode of chain orientation is virtually independent of lattice matching criteria. Dispersionrepulsive forces have been found to be most sensitive to orientation and greater in magnitude than the electrostatic forces.
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  • 22
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2237-2252 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Proton-decoupled, partially relaxed, Fourier-transform NMR of 13C in natural abundance was used to determine spin-lattice relaxation times of individual carbons of polyisobutylene, polyacrylonitrile, poly(vinyl chloride), and poly(vinyl alcohol) in solution. It is shown that the relaxation times are independent of the difference in stereochemical configuration. From the values of the nuclear Overhauser enhancement factor it is shown that the relaxation times are independent of the difference in stereochemical configuration. From the values of the nuclear Overhauser enhancement factor it is shown that the excess spin energy from equilibration of all the 13C, even of quaternary carbons, in the polymers dealt with here is transferred to the lattice mainly through 13C-1H dipolar interactions. It is shown that the segmental motions responsible for the spin-lattice relaxation of the polymer skeleton in solution can be described by the isotropic model within a good approximation, except for poly(vinyl alcohol) at low temperature. The activation energies of skeletal and internal methyl motions are estimated from the temperature dependence of the correlation time. Differences in the 13C line widths for individual carbons of polyisobutylene are discussed briefly.
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  • 23
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2283-2289 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The mechanism of non-Newtonian behavior for flow from the lower to the upper Newtonian region is explained by a modification of Graessley's theory. In the theory proposed here, a viscosity ηfric, which is based on friction between polymer segments and is almost shear-independent, is introduced in addition to Graessley's entanglement viscosity ηent, which decreases with increasing shear rate. The theory is applied to previously obtained data on steady flow of polydimethylsiloxanes of different molecular weights. The agreement between calculated and experimental results is good. In polymers with the molecular weight above the critical molecular weight for entanglement Mc, the major contribution to viscosity near zero shear rate is ηent. As the shear rate increases, the flow curve has an inflection where ηfric cannot be disregarded in comparison with ηent. In the upper Newtonian region, ηfric has more influence on the viscosity than ηent. The theory can also explain the experimental results on flow of polymers with molecular weight below Mc, which were shown to be slightly non-Newtonian in the previous paper.
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  • 24
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1375-1383 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Mean-square unperturbed dimensions 〈r2〉0 and dipole moments 〈μ2〉 have been calculated for propylene-vinyl chloride copolymers by means of rotational isomeric state theory. The calculations indicate that for these chain molecules 〈mu;2〉 is much more sensitive to chemical sequence distribution than is 〈r2〉0, a conclusion in agreement with results of previous studies of ethylene-propylene copolymers and styrene-substituted styrene copolymers. In the case of propylene-vinyl chloride chains, both 〈r2〉0 and 〈μ2〉 are most strongly dependent on chemical sequence distribution in the case of copolymers which are significantly syndiotactic in stereochemical structure. At equimolar chemical composition, increase in average chemical sequence length generally increases 〈r2〉0 but decreases 〈μ2〉. Under some conditions, values of these statistical properties go through a minimum with increase in the reactivity ratio product r1r2, thus complicating the use of experimental values of these properties in the characterization of chemical sequence distributions in these copolymers.
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  • 25
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1385-1411 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The molecular mechanisms involved in the orthorhombic-to-monoclinic phase transformation in polyethylene were investigated by the computer simulation of a structure-energy map based on empirically justified intermolecular potential functions. Stable packing structures for the orthorhombic and monoclinic form were isolated as relative minima, cohesive energies were determined from the energy minima, specific chain motions involved in the transformation were identified by the minimum energy path connecting the packing minima, and the activation energy for the transformation was determined from the energy barrier along the minimum energy transformation path. The packing structure parameters predicted from the energy map were in excellent agreement with unit cell dimensions observed near 0°K. The activation energy predicted for the transformation is relatively low (∼0.5 kcal/mole of ethylene at 0°K and 0.25 kcal/mole of ethylene near the melting point, 411°K). Monoclinic packing was predicted to be slightly more stable than orthorhombic. Since this result is inconsistent with a large body of observations, we propose that the intramolecular energy of chain folds plays a dominant role in establishing chain-packing geometry. The inclusion of fold-transition energetics could give rise to transformation mechanisms which differ in details from those proposed in this work.
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  • 26
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1413-1421 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Graft distribution functions have been derived from random grafting statistics. Among the functions, the weight fraction of ungrafted backbone chains, the molecular weight distribution of the ungrafted backbone chains and the GPC apparent molecular weight distribution of the graft copolymer have been found to agree with experimental values determined for a graft copolymer system in which grafting was expected to be random. The other functions, which are not directly measurable, are therefore probably also correct. In analytical work the entire set of graft distribution functions may be computed for a graft copolymer system from the following experimental data: (1) molecular weight distribution of the starting backbone chains; (2) the chemical composition of the mixture of the graft copolymer and ungrafted backbone; (3) the graft side-chain molecular weight distribution, which may be assumed to be identical to that of the ungrafted homopolymer separable from the reaction mixture.
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  • 27
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 109-116 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A model containing two rate constants is presented for the development of spherulites from sheaves. One, GR, is a radial spherulite growth constant while the other, GS, describes the rate of increase of apex angle of the sheaf. On the basis of this model, Avrami kinetics are developed which predict a change in the Avrami constant n from 5 to 3 as the sheaf develops into a spherulite. HV light-scattering patterns are calculated according to this model and are found to compare favorably with those found during the early stages of the crystallization of poly(ethylene terephthalate).
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  • 28
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 95-108 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Block copolymers having poly(tetrachlorobisphenol-A adipate) (PTBA) and polystyrene (PS) sequences were synthesized were synthesized by photodegradation of an oxime-containing polyester in the presence of styrene. Crystallinity, melting behavior, and spherulitic growth rates were studied as a function of block compositions and molecular weights. A model was proposed based on a complete phase separation between the two components. The influence of the polymer composition on the spherulitic growth rate is described by introducing a supplementary pre-exponential factor into the equation for the growth rate. This parameter is a measure of the tortuosity of the actual path that has to be covered owing to the presence of the noncrystallizable blocks.
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  • 29
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 117-135 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The nucleating activity of a large number of nucleating agents for the crystallization of polyolefins is not based on a high surface free energy of the substrate or on epitaxy, or on a minimum particle size just compatible with the thickness of the crystallizing polymer lamellae, or on any persistance of crystalline material in holes of the nucleating particles. The relevant mechanism is thought to be nucleation at steps of limited length in the surface of the nucleating particles. The nucleation is enhanced by a high degree of accommodation of polymer molecules at the surface of the substrate through the presence of ditches in the latter which cause prealignment of polymer chains and thus facilitate crystallization.
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  • 30
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Analytical expressions are derived for the concentration dependences of different apparent average (n,w,z) molecular weights for two types (end-to-end and segment-to-segment) of open association of polymolecular unimers. The open association is defined as an association leading to an unlimited number of multimer species. The type of association depends upon the number of associogenic sites per unimer molecule: for the end-to-end type this number is constant, whereas for the segment-to-segment type it is proportional to the degree of polymerization of the unimer. For the end-to-end association, a simple relation exists between the polydispersity (M̄r)w/(M̄r)n of the mul-timer and the association number r and the polymolecularity (M̄I)w/(M̄I)n of the unimers: (M̄r)w/(M̄r)n = 1 + r-1[(M̄I)w/(M̄I)n - 1]. The z-average and higher averages of the r-mers may be lower than the corresponding averages of the unimers. In the theta-state, (M̄n)app,Θ and (M̄w)app,Θ are linear functions of c/(M̄n)app,Θ, whereas a more complicated relation exists for the apparent higher averages. For the segment-to-segment association, both (M̄w)app,Θ and (M̄z)app,Θ are linear function of the weight concentration c, whereas no closed expression could be found for (M̄n)app,Θ. For the polydispersities of multimers one finds (M̄I)z/(M̄r)w = 1 + r-1[(M̄I)z/(M̄I)w - 1], and, in the special case of a Schulz-Zimm distribution of unimer molecular weights, (M̄r)n/(M̄r)w = 1 + r-1[(M̄I)n/(M̄I)w - 1].
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  • 31
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 175-191 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The complex dielectric constants ∊* = ∊′ - j∊″ of each of several members of a system of copolymers of 4-chlorostyrene and 4-methylstyrene have been measured from 1.6°K to 300°K and from 0.1 kHz to 20 kHz. The principal experimental findings are: the strength of the relaxation process which occurs near 50°K at 1 kHz varies linearly with changing copolymer composition; both the apparent activation energy (H = 2.7 ± 0.7 kcal/mole) and the shape of the relaxation curve are independent of the composition variable and of the temperature (or frequency) within the ranges studied; and the ratio of the relaxation strength of poly-4-methylstyrene to that of poly-4-chlorostyrene in the 50°K process is about 25 times the corresponding ratio for the primary relaxation process that occurs in the neighborhood of the glass-transition temperature. These findings suggest that in the 50°K process the phenyl groups relax independently of one another; that the apparent activation energy and the shape of the relaxation spectrum are determined primarily by the nature of the intrachain forces; and that the strength of the relaxation process depends primarily on effects of intermolecular forces that are governed by the molar “free volume” of the copolymers.
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  • 32
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 149-173 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The theory of small-angle light scattering was developed for oblique incidence of the light beam on the surface of a two-dimensional spherulite. Results of the theory were compared with previously reported results of light scattering from two-dimensional and three-dimensional spherulites for normal incidence, and with some experimental patterns. The comparisons suggest that the scattering intensity distributions of two-dimensional spherulites deviate from those of three-dimensional spherulites when the sample surface is tilted with respect to the propagation direction of the incident beam, although they are almost identical when the sample surface is normal to the incident beam. Observation of the change of scattered intensity distributions upon tilting the samples thus provides a method of distinguishing between two-dimensional and three-dimensional spherulites. Moreover, this observation makes it possible to determine the degree of planar orientation of the optic axes of optically anisotropic scattering elements within two-dimensional spherulites. The calculations were carried out for special cases of two-dimensional spherulites with the optic axis orientation confined to the two-dimensional plane and randomly or helicoidally rotated around the spherulite radii.
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  • 33
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 233-248 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystal structure of α-gutta percha has been determined by x-ray diffraction. The unit cell parameters are a = 7.98 Å, b = 6.29 Å, c (fiber period) = 8.77 Å, and β = 102.0° (monoclinic). The space group is P21/c-C2h5. Two molecular chains of nearly trans-CTS-trans-CTS̄ conformation pass through a unit cell; C, T, S, and S̄ being the cis, trans, and two types of skew forms, respectively. The constrainedle astsquares method was modified so that the order of the least squares matrix could be reduced and was applied to the refinement of the crystal structure.
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  • 34
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 275-287 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: As model polymers for isolated short-chain branches in low-density polyethylene, a series of ethylene-1-olefin copolymers was examined by use of 13C NMR at 25.2 MHz. An array of 13C resonances was observed that could be associated independently with methyl through amyl branches. The 13C chemical shifts became insensitive to branch length with hexyl and longer branches. Assignments of the various carbon resonances associated with branching were accomplished by using off-resonance decoupling techniques and the behavior of alkane chemical shifts previously observed by other investigators. The ratio of certain backbone and branch resonances could be used to establish the short-chain branch distribution in a low-density polyethylene.
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  • 35
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 289-296 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The question of viscous flow versus molecular diffusion mechanisms for pressure-induced liquid transport through membranes is critically examined for the specific case of homogeneous swollen membranes. It is shown that previous attempts to compute diffusion coefficients from hydraulic permeabilities for such systems have used an equation which is grossly in error. It estimates diffusion coefficients which are orders of magnitude too high and often exceed self-diffusion coefficients. This has frequently led to the conclusion that viscous flow predominates. The origins of the errors in this equation are indicated, and a substitute equation is developed which gives diffusion coefficients well below that for self-diffusion when applied to literature data. As a result it is concluded that molecular diffusion is the dominant mechanism in homogeneous systems.
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  • 36
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 297-311 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Stress-strain behavior in extension and the swelling of polymer networks with different lenghts of crosslinks is reported. These networks were prepared by copolymerization of butyl acrylate with different amounts of various difunctional comonomers which yield crosslinks of 4, 7, 10, and 16 bonds in length. The efficiency of the comonomers in crosslinking is low, improving with increasing length of the chain between their unsaturated endgroups. Analysis of a large number of stress-strain data obtained at elongations between 2 and 8% elongation showed that in this deformation range the stress-strain relation based on the statistical theory of elasticity represents the data better than does Hooke's law or the Mooney-Rivlin relation. It was found that the relation between the modulus at small deformations and the swelling ratio of the various samples inindependent of the length of the crosslinks. Also the shapes of the Mooney-Rivlin curves are the same for all networks. Furthermore, the creep behavior of various networks with different crosslink lengths is the same for networks compared at the same elastically effective chain concentration. It is concluded that the lenght of the crosslinks, at least up to 16 bonds, does not affect the elastic response of polymer networks.
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  • 37
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2027-2037 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A model incorporating reversible, bimolecular immobilization for diffusion and sorption in glassy polymers is developed. Sorption is considered to occur by two distinct mechanisms: ordinary diffusion-controlled sorption and sorption resulting from the immobilization of diffusing gas molecules by prexisting sites in the polymer. Expressions are obtained for equilibrium sorption, transient sorption, and time lag. The effects of kinetic parameters of the model are illustrated and discussed.
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  • 38
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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 orientation behavior of regenerated cellulose, in both crystalline and noncrystalline phases, was investigated quantitatively under various conditions during coagulation-regeneration from viscose solution and during drying of the resulting gel film. It was concluded that the stronger the tensions which arise parallel to the film surface during coagulation-regeneration and drying of the gel film, the more prominent become the uniplanar orientation of the (101) crystal plane and planar orientations of the crystal b axis and noncrystalline chain segments, all parallel to the film surface and associated with considerable distortion and disintegration of the regenerated crystal. This conclusion suggests an orientation mechanism of the cellulose II crystal, namely, rotation of the crystal around the U(101) axis associated with slippage of the (101) crystal plane, the most highly hydrated and most readily dislocated plane, in the direction of the tension, which is also parallel to the surface of the film. The behavior of this type of uniplanar orientation of the (101) crystal plane is characterized semiquantitatively by comparing observed distributions of the orientation of crystallographic axes with those calculated on the basis of a relatively simple model for crystal orientation.
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  • 39
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2135-2142 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An attempt was made to evaluate stresses on chemical bonds in axially stressed polymers from the shift of skeletal vibration frequencies in chain molecules. The maximum stress on chemical bonds was found to be at least ten times the average stress on the specimen.
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  • 40
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2153-2171 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Specimens of poly(vinylidene fluoride), crystal form II, annealed at different temperatures between 130 and 180°C were characterized by specific volume measurements, differential scanning calorimetry (DSC), and electron micróscopy. The degree of crystallinity calculated from the specific volume changed only by 15% i.e., from 50% to 65%. On the other hand, the melting behavior changed with annealing conditions. When a specimen was annealed above 170°C, two endothermic peaks appeared on either side of the annealing temperature. Results from DSC measurements made at different heating rates and electron microscopy showed that the two endotherms were caused by a bimodal distribution of lamellar thicknesses. The equilibrium melting point was found to be 210°C from the linear relation of the melting point and the annealing temperature. The equilibrium enthalpy and entropy of fusion were found to be 1.6 keal/mole and 3.3 eu/mole of repeat units by measurement on polymer-diluent mixtures. The surface free energy was found to be 5.1 kcal/mole of lamellar sequences from the plot of melting point versus reciprocal lamellar thickness obtained by electron microscopy. From a plot of enthalpy of fusion versus reciprocal lamellar thickness the surface enthalpy was found to be 20 keal/mole of lamellar sequences. These data lead to the estimate that a chain fold consists of about 30 repeat units.
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  • 41
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 457-465 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An approximate model is developed which relates the twisting seen in the spherulitic crystallization of many materials to surface stresses. Expressions are presented for the twist period as a function of the surface stress. These are compared with previous experimental data on polyethylene and data on hippuric acid obtained in the present investigation. In both cases the experimental data are in accord with the predictions of the model.
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  • 42
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An examination of powder x-ray diffractograms of native and hydrolyzed cellulosic materials obtained from widely different sources revealed the presence of materials having a higher degree of molecular order than ramie hydrolyzate, the conventional crystalline standard for cellulose. With the use of these materials as new crystalline standards, a critical reappraisal has been made of the validity of the application of the two-phase (i.e., fringed-micelle) hypothesis to the fine structure of cotton and related cellulosic materials. It is concluded that the lattice structure of cotton and related celluloses of plant or bacterial origin is liquid-like or paracrystalline.
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  • 43
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 467-486 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In order critically to evaluate the previous morphological interpretations of stress relaxation during oriented crystallization, a reexamination was made of the relaxation behavior of the same oriented natural rubber material used for the x-ray investigation in Part II of this series. Our results were found to be in qualitative agreement with previously published reports. Comparison of stress-relaxation rates at low temperatures for samples with strains of 200% or more with crystallization rates at room temperature by others for similar elongations indicates a dual nature in the strain-induced crystallization process. This conclusion is in full agreement with the indication of dual crystalline morphologies, namely, fibrillar and lamellar, for both electron microscopy and x-ray investigations on highly stretched samples reported in Parts I and II. Examination of stress-relaxation data in light of morphological evidence for oriented crystallization indicates that caution must be exercised in attaching morphological significance to the Avrami exponent n obtained from stress-relaxation or crystallization data.
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  • 44
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 511-527 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Although samples of amorphous polymers cast from solution are usually assumed to be isotropic, they may, in fact, have some anisotropy due to the Bénard effect, in which the convection currents produced by evaporation are organized into a regular arrangement of cells. A pattern of hexagonal convection cell is easily visible during casting of SBS triblock copolymers. The anisotropy is demonstrated by comparing the small-angle x-ray diffraction diagrams taken through the face and edge of the films. The domain structures in two SBS copolymers are characterized by diffraction measurements. The smallangle diagram of a triblock polymer containing 50% styrene indicated a lamellar structure, while that from a 28% styrene copolymer is interpreted as arising from a hexagonal array of polystyrene cylinders dispersed in a continuous polybutadiene phase. Published diffraction data for block copolymers and other amphiphiles are surveyed in an attempt to place some limitations on the composition ranges over which the various types of domain structure exist. The factors which determine the dimensions of the two domains in lamellar phases formed from diblock copolymers are examined theoretically, and the predicted dimensions are compared with experimental results.
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  • 45
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 499-510 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The partial molar excess free enthalpies and enthalpies as well as the molar excess enthalpies of a number of n-alkane systems were reexamined within the scope of the polymer solution theory of Flory, Orwoll, and Vrij and that of Prigogine in the version after Delmas, Patterson, and Somcynsky. A semiempirical method was used to obtain characteristic n-alkane data, which obey the principle of corresponding states. By using these data (instead of those from the partition function after Flory and collaborators), a physically realistic interpretation of the excess free enthalpies over the whole concentration range is possible if the combinatorial contribution is purely athermal in nature. Both theories give an enthalpy interaction parameter near zero as expected, whereas neither a significant end effect nor an entropic interaction contribution is apparent from the analyses of the excess free enthalpies. The poor results obtained for the partial excess enthalpies and the enthalpies of mixing reflect the inadequacy of the partition functions on which these modern solution theories are based.
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  • 46
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 529-538 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A method based on use of NMR and infrared spectroscopy is described for the quantitative determination of the structural units generally occurring in polyalkenamers. The possibilities offered by both techniques are pointed out: in particular, the values found for the absorptivities of the infrared bands typical of unsaturated alkenamer units are extensively discussed.
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  • 47
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 807-811 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 5 Ill.
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  • 48
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 813-813 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 49
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 929-938 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: By means of an extrusion technique, a uniformly oriented macrolattice based on an alternating sequence of polystyrene and polybutadiene lamellae has been obtained. This is confirmed by the techniques of low-angle x-ray diffraction, electron microscopy, and electron diffraction. Layer thicknesses and spacings have been derived, and good quantitative agreement exists between the values obtained by the different methods. In addition, the electron micrographs exhibit many singular features which are of potential importance both in their own right and for the macroscopic properties.
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  • 50
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 951-971 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A surface zone composed of at least three distinct layers has been detected in injection-molded polypropylene. The morphology of these layers as determined by optical and scanning electron microscopy forms a continuous picture from the “as-molded” surface to the core. With the exception of the first layer which is always featureless, the observed morphology is mostly spherulitic. Starting in the second layer, the spherulites decrease steadily in size until they reach a minimum somewhere near the middle of the third layer. After passing this point, they increase in size - rather rapidly - as the boundary between layer 3 and the core is approached. In samples prepared at the shorter fill times, the spherulites continue to decrease in size until they are replaced by the mixed matted straw-flat plate texture. The overall morphological features of this surface zone are explained by using an extension of a model for the crystallization of a quiescent polymer melt. In this model, growth originates from heterogeneous nuclei whose density varies throughout the sample as a function of both a temperature gradient and the induction time. Interpretation of anomalies in the fine structure of the individual layers indicates that shear is influencing the crystalline morphology also.
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  • 51
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1013-1021 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Modification of the Griffith theory for the presence of liquids has been shown to explain some facets of the environmental stress cracking of polyethylene. In the absence of intercrystalline links and tie molecules, we find that one important factor is the interfacial tension generated between the spherulite boundary and the liquid environment. Judicious incorporation of silanes into polyethylene appear to reduce the tendency to stress cracking by modifying the interfacial tensions between the environment and the polymer.
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  • 52
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1189-1200 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The parameters in the Mark-Houwink relationship, [η] = K′M̄va, for linear polyethylene in 1-chloronaphthalene and 1,2,4-trichlorobenzene at 130°C have been estimated. They were found by measuring the limiting viscosity numbers of a series of fractions with molecular weights ranging from less than 10,000 to almost 700,000. The results are for 1-chloronaphthalene, [η] =0.0555 M̄v0.684 (with a standard error of 0.0064 in K′ and 0.010 in a) and for 1,2,4-trichlorobenzene, [η] = 0.0392M̄v0.725 (with a standard error of 0.00703 in K′ and 0.015 in a), where [η] is expressed in ml/g. The unperturbed end-to-end distance calculated from the viscosity-molecular weight data agrees with the theoretically expected value.
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  • 53
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1201-1218 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The elastic displacement of an axially stressed chain within crystalline surroundings, which was first treated by Chevychelov, is reexamined. We compare the results obtained for homogeneously distributed masses with that for discrete atoms, considering the nonuniformity of the potential of a crystal containing hydrogen bonds. In polyethylene and polyamide the maximum mechanical excitation of a chain penetrates into the crystal a distance of 15 to 20 chain atoms. The effect of the relative position of the crystal boundary on the stress-strain field was studied and the energy of defects calculated.
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  • 54
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1219-1233 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A New method for evaluating SAXS curves of polymer samples with lamellar structure is applied to two typical scattering curves measured with a solution-crystallized linear polyethylene and a melt-crystallized branched polyethylene respectively. The method permits a rigorous check of the validity of the two-phase model and yields, without additional measurement, the volume fractions of the two phases and the difference in their densities. The densities can than be obtained by measuring the overall density of the sample. The results are: ρc = 0.996 g/cm3,ρa = 0.854 g/cm3, wa = 0.20 for the solution-crystallized sample; ρc = 0.967 g/cm3,ρa = 0.850 g/cm3, wa = 0.36 for the melt-crystallized sample.
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  • 55
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1235-1245 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Creep failure in oriented nylon 6 fibers has been studied. The results suggest that the variations in the lifetime under various loading histories are inherent, but statistical, characteristics of the material itself. The treatment of experimental data by a stochastic theory shows that the creep failure can be regarded as a nucleation process. An interpretative analysis of the structural changes during creep indicates that the nucleation is brought about by bond rupture in the amorphous regions of the fiber structures.
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  • 56
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1263-1269 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Shape changes in the electron spin resonance spectrum of spin-labeled polystyrene have been studied as a function of temperature in the range 77-340°K. Rotational correlation times have been calculated by using recent theories of slow-motional effects on ESR spectra. Three models were used, namely, Brownian, moderate jump diffusion, and large jump diffusion. The moderate jump model gave correlation times in good accord with those found by other techniques for the δ relaxation in polystyrene. The relaxation was found to be independent of molecular weight.
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  • 57
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1285-1292 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A theoretical determination of the elastic modulus, the breaking strength, and breaking strain is made for a single infinitely long molecule of polyethylene (CH2)∞. These results are compared with those of a similar calculation on a molecule of polyethylene with a side chain attached. It is found that the presence of a side chain weakens the molecule by approximately 17%.
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  • 58
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1251-1262 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The composition heterogeneity has been calculated for some block and graft copolymers. General relationships have been derived for a model of the poly(A-g-B) or poly-(A-b-B) type fulfilling the assumption of random grafting. Numerical results have been calculated for special cases of particular interest. These include a copolymer having independent molecular weight contributions from units of species A and B (a special case of which is a block copolymer) and a graft copolymer where the grafting is not accompanied by crosslinking or degradation side reactions and no homopolymer B is formed. Two other model systems represent the effects of the presence or absence of both homopolymers. For the above models, the dependence of the composition heterogeneity on the structure-determining parameters (average number of grafts in the molecule, polydispersity index of the molecular weight of the backbone and graft) is discussed. The heterogenities thus calculated are in many cases comparatively low. The composition heterogeneity of the system is in most cases increased by the presence of homopolymers.
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  • 59
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1331-1336 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The relation between the fractive index n and the density ρ of a liquid mixture is formulated as \documentclass{article}\pagestyle{empty}\begin{document}$$ {{\left( {n^{{2 \mathord{\left/ {\vphantom {2 3}} \right. \kern-\nulldelimiterspace} 3}} - 1} \right)} \mathord{\left/ {\vphantom {{\left( {n^{{2 \mathord{\left/ {\vphantom {2 3}} \right. \kern-\nulldelimiterspace} 3}} - 1} \right)} {\rho = }}} \right. \kern-\nulldelimiterspace} {\rho = }}\sum\limits_i {w_i R_{Si} } $$\end{document} where wi and Rsi are the weight fraction and the specific refraction, respectively, of component i. The calculation of the specific refraction of straight-chain polyethylene and polystyrene from data for pure compounds of low molecular weight is discussed. The result is applied to dilute solutions of polystyrene in toluene. The calculated values of (dp/dw)0 and (d2ρ/dw2)0 at three different temperatures are compared with measured values. The agreement is satisfactory.
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  • 60
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1465-1475 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Graessley's theory of non-Newtonian behavior of linear polymers is tested with data on polyethylenes and polypropylenes having a wide range of molecular weights and molecular weight distributions, and for a polyethylene fraction. Theoretical flow curves derived by using molecular weight distribution data from column fractionations are in good agreement with experimental curves obtained from a cone-and-plate viscometer and an extrusion-type rheometer, when the distribution is assumed to cut off at a maximum molecular weight. The experimentally obtained relaxation time for entanglement is found to be proportional to the Rouse relaxation time, though the former is about one decade smaller than the latter.
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  • 61
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1793-1801 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Chain folding in unoriented poly(ethylene terephthalate) (PET) films has been investigated as a function of annealing time and temperature. To meet this objective dynamic mechanical, infrared, and molecular weight measurements were used, together with selective chemical degradation to remove chain folds and amorphous regions. The β dispersion in the dynamic mechanical spectrum of PET is here tentatively associated with motions of methylene and/or carboxyl groups in irregular chain folds; the β dispersion is not found in quenched amorphous polymer, in polymer where amorphous regions and chain folds have been removed, or in highly annealed PET where the irregular folds have regularized. Upon mild crystallization and annealing (30 min at 110°C) of initially amorphous film a large β dispersion appears and then diminishes upon further annealing at 220°C. As the β dispersion diminishes, the infrared regular fold band increases more than the crystallinity band, indicating regularization of folds. The molecular weight of the degraded residue corresponds approximately to typical fold-period dimensions (∼130 Å), and increases on annealing as expected from lamellar thickening. The degradation process has, by fold removal, reduced the chains in the crystals to a very short, uniform length.
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  • 62
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1829-1839 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The sorption and diffusion of gases in poly(ethylene terephthalate) (PET) films have been measured by using a newly devised apparatus which gives the sorption rate curves from the initial to the equilibrium state. By analysis of sorption data for carbon dioxide in PET film, it was shown that the diffusion rate, as well as the equilibrium solubilities, could be explained by the dual-mode sorption mechanism proposed by Vieth et al. Constants of their equation were used in the analysis of our experimental results, in which the apparent diffusion coefficients were dependent on pressure. The result showed that the dual-mode sorption mechanism indeed applies to diffusion. The value of the real diffusivity obtained in amorphous PET was 5.7 × 10-9 (± 8%) cm2/sec in the range of pressure from 0 to 1 atm. It is believed that this apparatus has wide applicability, not only to diffusion of gases in polymers, but also to the measurement of surface properties, and can be used to study the morphology of a variety of polymers.
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  • 63
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1855-1857 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 64
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1867-1872 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dependence of the magnitude of the permeation flux on the sense of flow is studied in the case of a simple membrane laminate AB. The permeability of phase A is assumed to change from a low value at low permeant activity to a higher one at high permeant activity, whereas the permeability of phase B is constant. The results of the analysis of this simple system provide considerable insight into the factors influencing flow reversal effects in binary laminated membranes in general. The conditions under which marked effects of this kind are possible have been established.
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  • 65
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1873-1878 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dynamic mechanical properties of the ultrahigh molecular weight nylon 66 film and fiber produced by thermally induced solid-state polycondensation are presented. The α peak temperature of tan δ of these treated films and fibers is shifted 8-32°C higher than that of the appropriate control nylon 66 (film and fiber) while the maximum height of the tan δ peaks is decreased. The treated fibers have higher moduli at all temperatures (20-145°C) and humidities (30% RH) than do their control counterparts. The moduli of the treated fibers at 30% RH compare favorably with control yarn at 0% RH. These yarns also have a greater per cent of the 25°C modulus retention as temperature increases.
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  • 66
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1941-1948 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An expression for the flow field resulting from a time-dependent force with time-dependent point of action is derived from the linearized Navier-Stokes equations. The result is written as a sum of terms, the first of which is the “slow-change limit” corresponding to a stationary force acting at a stationary position. The application to the steady rotation of a dumbbell shows that this sum corresponds to a series expansion in powers of (L2|Ω|/v)1/2 where 2L is the length of the dumbbell, Ω is its angular velocity, and v is the kinematic viscosity of the liquid. It is pointed out that the results obtained are relevant to the problem of rotatory Brownian motion and to that of non-Newtonian viscosity.
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  • 67
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2173-2184 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Relative tilt between two similar thin crystals may result in the formation of a moiré pattern in the electron image. Patterns hitherto interpreted as being parallel moirés or rotation moiré obtained from overlapping solution-grown polymer crystals are reconsidered, and it is shown that in some cases a tilt model is more acceptable. The general features of tilt moiré patterns predicted for crystals of this kind are discussed and compared with micrographs appearing in the literature. Methods of distinguishing tilt moiré patterns are indicated, though it is admitted that such experiments would be difficult to complete in the time limited by destruction of the crystal structure under the action of the electron beam. Extinction contours may also sometimes be confused with long-period tilt moiré patterns, and again careful experimentation is required for accurate identification. The model of the structure of solution-grown polyethylene crystals inferred from a tilt moiré interpretation of many of the electron image fringe patterns found in the literature is consistent with that derived from other sources.
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  • 68
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2001-2012 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polarized infrared absorption spectra have been obtained by Fourier-transform spectroscopy for several crystalline and noncrystalline absorption bands of polyethylene crystallized by orientation and pressure in capillary viscometer. An analysis of data obtained at room temperature yielded degrees of crystallinity which are in good accord with values obtained from calorimetry and density measurements. The dichroism of the infrared absorption bands for the crystalline region revealed an extreme degree of orientation consistent with previous x-ray studies and also demonstrated that the degree of orientation is a good or better than that obtained from drawn polyethylene films with extension ratios of 20. Dichroism of bands from the amorphous phases revealed that the noncrystalline chain segments are in a comparatively relaxed state compared with results for drawn films having extension ratios of about 2 to 7. This is 1/10 to 1/3 the extension ratio of drawn polyethylene which shows maximum crystalline orientation. The results also indicated that the ratio of the GTG′ to GG segment conformations in the amorphous regions is larger than that of amorphous portions in unoriented polyethylene. The vinyl endgroups were shown to be highly oriented, while the main bulk of the amorphous polymer was fairly relaxed, i.e., of low orientation. It is concluded that the amorphous polyethylene state is strongly dependent on the nature of the crystalline-amorphous interface.
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  • 69
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2089-2098 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The sorption behavior of particulate-filled resin composites is discussed and related to several different models. A thermodynamic analysis of the sorption is presented in the form of a cycle for the changes in Gibbs free energy. From such an analysis it is possible to set up a scale of relative adhesion between filler and resin matrix. It is shown that the scale depends on the sorbate, but use of this scale will rate the adhesion between resin and filler in the correct relative order.
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  • 70
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2371-2376 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In measuring sinusoidal normal stress difference of concentrated polymer solutions in a Weissenberg rheogoniometer, the resistance to motion of the upper platen due to the sample between the cone and plate should be taken into account. Correction terms are derived. The theoretical predictions of Lodge and others concerning the relationship between oscillatory normal stress difference and oscillatory shear stress are found to agree with experimental data if these corrections are applied.
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  • 71
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2403-2411 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The molecular conformation and the crystal structure of α-form poly-p-xylylene has been determined by x-ray diffraction. The polymer has a monoclinic unit cell with a = 5.92, b = 10.64, c (fiber axis) = 6.55 Å, and β = 134.7°. Two chains pass through the unit cell, and the space groups is C2/m. The packing fraction is 0.705. One monomer unit makes up the fiber identity period and the internal rotation angles are 0° and 90° for the —CH2—CH2— and —CH2—φ— bonds, respectively. All benzene rings are in parallel orientation, perpendicular to the ac plane.
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  • 72
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2441-2451 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: For a polymer in which permanent rupture of individual molecules is the rate-limiting process for plastic deformation, the kinetics of chain-end diffusion and secondary radical reactions should be compared with the kinetics of caged radical recombination in the calculation of activation parameters for plastic deformation. If mechanisms of cage escape are slower than those for cage recombination, the activation parameters for plastic deformation will differ from those for the initial bond-breaking process. For the case of polyethylene deformed in the vicinity of 250°K, the critical thermally activated event appears to involve scission of the polymer molecule near the site of an abstracted hydrogen atom. For this system the dominant cage-escape mechanism is diffusion, which is faster than either hydrogen abstraction or unzipping to the monomer. However, at low stresses the rate of cage recombination is expected to be higher than the rate of cage escape, so that the activation parameters for deformation should be the sum of those for chain scission and diffusion. The contribution of diffusion (ca. 15 kcal/mole) to the activation energy for deformation (E*, extrapolated to zero stress conditions) is relatively modest. However, the calculated molar activation volume for deformation V* increases by almost an order of magnitude, i.e., from ca. 10 to ca. 76 cm3/mole when diffusion is required. Consideration of experimental values of E* and V* for high molecular weight polyethylene indicates that, in the regime examined, chain scission plus chain-end diffusion is required to effect plastic deformation.
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  • 73
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1-14 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A homologous series of aliphatic polyoxamides, nylon 122, 102, 82, and 62, were prepared by the bulk polycondensation of dialkyl oxalates with diamines. Infrared spectroscopy, x-ray diffraction, differential thermal analysis, thermogravimetric analysis, and gas chromatography were used to study the structure and thermal stability of these polyoxamides. From the fiber pattern of nylon 122, a structural repeat distance of 19.5 Å was measured. This was in close agreement with the expected value for an extended planar, zigzag chain conformation. With the exception of the expected decrease in the structural repeat distance along the chain axis resulting from the different number of methylene groups, nylons 122, 102, and 82 were isostructural. Nylon 62 appeared to pack in a similar manner to the other materials studied. However, there were differences in the diffraction pattern of this polymer; these may be indicative of a different chain conformation or of strain in the crystalline regions of the polymer. The infrared spectra indicate the presence of strong hydrogen bonding in all the polymers. Thermal analysis and pyrolysis data revealed catastrophic polymer degradation between 400 and 500°C in nitrogen, with appreciable homolytic cleavage of the oxamide group.
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  • 74
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 25-30 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It is shown that an optically excited current in polyethylene does not interact with the dark absorption current. This implies that the carriers are different for the two processes. We suggest that holes are photo-injected and traverse the full thickness of the specimen, while the absorption currents are due to surface barrier processes, as proposed by other workers.
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  • 75
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 193-200 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Previously it was found that the lamellar thickness of solution-grown polyamide crystals as assessed by low-angle x-ray diffraction appeared to be unaffected by crystallization conditions. This point has now been re-examined in detail on nylon 6.6 with crystallization temperature Tc as the main variable. Over a very wide range of Tc the lamellar thickness was invariant; a notable increase could be produced only at the highest Tc. The “invariant” lamellar thickness occurs at larger supercoolings than can be realized in the much-studied polyethylene, which may explain why it has not yet been reported for polyethylene. The existence of this minimum invariant value raises important questions concerning the applicability of the current kinetic theories over such a wide range of supercoolings. Several other polyamides also revealed invariant long spacings after crystallization from solution. This provides the justification sought for comparing, in the paper which follows, the long periods observed for a large number of polyamides.
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  • 76
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 201-216 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of linear, aliphatic polyamides in which the number of carbon atoms in the repeat unit ranged from three to twenty-four was crystallized from solution. All gave lath-shaped crystallization products (usually aggregated in the form of sheaves) that were unmistakable lamellar. Sedimented mats of the crystals were examined by lowangle and wide-angle x-ray diffraction. Each polyamide had a characteristic layer thickness (fold length) which was determined by the length of the repeat unit and the number of hydrogen bonds in the lamella. The thickness was independent of other variables examined including crystallization conditions. The polyamides studied cover a wide range: they border on polypeptides at the one extreme and approach polyethylene at the other. For all these materials there emerged a unifying pattern which relates chemical structure directly to chain folding.
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  • 77
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 217-221 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Nylon 6 in the form of bundles of fibers or rods was treated to contain traces of chloranil of other quinones. When stressed within an EPR cavity, the radicals produced were trapped in a relatively stable form containing the quinone. This method offers a quantitative measurement of the integrated number of free radicals produced during a stress history.
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  • 78
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 249-264 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Melting points and lamellar thicknesses have been measured for ethylene oxide-propylene oxide block copolymers (sym-PEP) with central poly(ethylene oxide) block lengths of 70-100 chain units and end poly(propylene oxide) block lengths of 0-30 chain units. Melting points of the block copolymers are lower than those of the corresponding poly(ethylene oxide) homopolymer by an amount (up to 15°C) which increases as the poly(propylene oxide) block length increases. Most samples have more than one melting transition, which can be assigned to variously folded chain crystals. End interfacial free energies σe for the various crystals have been estimated by use of Flory's theory of melting of block copolymers. For a given crystal type (e.g., once-folded-chain) σe is higher the longer the chain length of the end poly(propylene oxide) blocks. For a given copolymer σe is lower, the more highly folded the poly(ethylene oxide) chain.
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  • 79
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 265-268 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Melting points have been measured for several ethylene oxide-propylene oxide block copolymers (sym-EPE) chosen from the Pluronic range. Melting points of the block copolymers are lower than those of the corresponding poly(ethylene oxide) homopolymer by up to 4°C. The melting point depressions are much smaller than those observed for comparable sym-PEP block copolymers.
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  • 80
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 269-273 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dependence of joint strength upon the molecular weight between crosslinks Mc of an adhesive has been investigated for joints which consist of a crosslinked, amorphous rubber adhering to a rigid polymeric substrate. The joint strength was found to be independent of Mc if results were compared at the same effective rate of testing. If, however, values of joint strength were compared at a particular test temperature and rate, the joint strength generally increased as the value of Mc decreased. This result can be explained by the increase of the glass transition temperature of the adhesive with increasing crosslink density.
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  • 81
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 389-390 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Tab.
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  • 82
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 369-388 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: One of the cyclic oligomers of formaldehyde, 1,3,5,7,9,11-hexoxecane, was found to undergo polymerization in the solid state to form polyoxymethylene both during and subsequent to x- or γ-irradiation. The polymer yield increases with polymerization temperature but decreases drastically near the melting point of the hexoxecane crystal. In order to clarify the specificity of the solid-state polymerization, the crystal structure of hexoxecane was first analyzed; hexoxecane forms a trigonal crystal with cell dimensions of a = b = 7.917 Å, c = 11.345 Å, space group R3-C3i2, three molecules of 3 symmetry per unit cell. The polyoxymethylene as polymerized from a single crystal of hexoxecane is highly crystalline and the crystallites are definitely oriented with respect to the original crystal. There are three kinds of oriented trigonal polyoxymethylene: i.e., with the polymer chains oriented along the 〈100〉, 〈001〉, and 〈210〉 axes of the hexoxecane crystal. The relative yields of these crystallites depend upon the polymerization temperature. In addition to the ordinary trigonal polyoxymethylene, oriented orthorhombic polyoxymethylene was also found in the case of polymerization during treatment with x-rays.
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  • 83
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 393-395 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 84
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 397-398 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
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  • 85
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 399-411 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The molecular weight distribution in various celluloses degraded with hydrochloric acid has been studied by gel-permeation chromatography. Measurements were made on the residue after hydrolysis, on the degradation products solubilized by the acid, and on whole degraded samples comprising the product soluble in the acid plus the residue. It is shown that the total number of crystallites decreases during hydrolysis while the chain length distribution remains constant. The crystallites are gradually broken down into molecular fragments which show a size distribution centered on species with a degree of polymerization of about 8. Possible interpretations of these results are discussed.
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  • 86
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 571-585 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An x-ray study has been made of the structure of a series of ethylene-phosphonic acid copolymers and the parent low-density polyethylene from which they were derived. The phosphonic acid contents (groups per 100 carbon atoms) of the copolymers were: A, 0.8; B, 1.8; C, 2.8; and D, 8.0. Small-angle x-ray scattering (SAXS) results show that the phosphonic acid substituents do not incorporate into the crystal lattice to any appreciable extent, that the substituents have the effect of decreasing the average thickness of the crystal lamellae and increasing the breadth of the size distribution of thicknesses, and that a two-phase model does not adequately account for the observed SAXS invariant. Wide-angle x-ray scattering (WAXS) results show that specimens, A, B, and C are partially crystalline with the polyethylene crystal structure and that D is amorphous. The observed broadenings of the 110 and 200 crystal reflections in the copolymers indicate that the substituents decrease the lateral dimensions of the crystalline lamellae and/or increase the deformation of the lattice due to external strain. Specimen D, completely amorphous according to the WAXS criterion, exhibits the largest value of the SAXS invariant of all the copolymers studied and must thus possess a multiphase structure consisting of small ordered regions and a disordered phase. The results of the study show the structure of the copolymers to be consistent with the fringe-micelle model but do not rule out the folded-chain model, although a regular fold surface is unlikely.
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  • 87
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 587-593 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Internal motions in an alternating copolymer of ethylene and tetrafluoroethylene were investigated by dynamic mechanical and dielectric measurements and by nuclear magnetic resonance. At 1 Hz the α, β, and γ relaxations were observed at 110, -25, and -120°C in a quenched sample. The activation energy was 76 kcal/mole for the α relaxation and 10.6 kcal/mole for the γ relaxation. These relaxations are attributed to the motion of long and short segments in the amorphous regions, respectively. The β relaxation, which was observed only in the dynamic mechanical experiments, appears to occur in the crystalline regions. The copolymer is isomeric with poly(vinylidene fluoride), but it has a higher melting point and a much lower dielectric loss.
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  • 88
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 737-758 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dielectric dispersions of reconstituted collagens and gelatin were measured from 0.1 to 10 kHz and -160 to +160°C. At 0.1 kHz there is a γ transition at -80°C which is attributed to the H2O-coupled local modes. The process has an activation energy of 7.5 kcal. A devitrification process is observed at 10-20°C. Both of these processes have their counterparts in the dynamic mechanical measurements. The tan δ values are up to 3 times as great for the dynamic mechanical dispersions. There is an additional hightemperature dielectric loss transition which does not correspond to any seen with the mechanical experiments. A probable mechanism for this absorption is the Maxwell-Wagner-Sillars effect.
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  • 89
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2143-2152 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Based upon the high-temperature solid-state dielectric behavior of H-Film and supporting evidence from infrared spectroscopy, heat capacity, thermal expansion, and dynamic mechanical measurements, it is concluded that the actual chemical structure of H-Film is far more complex than previously expected. The very unusual thermal properties of this polymer, such as lack of a glass transition temperature, its extreme insolubility, and high dielectric losses above 250°C with only weakly corresponding mechanical losses, suggest that in addition to the pyromellitimide repeat unit, a significant part of the structure consists of amide groups, probably in the form of crosslinks.
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  • 90
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2199-2208 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Lexan polycarbonate specimens in the form of tubes were deformed in torsion. The deformation occurs by the nucleation and growth of discrete shear bands. Shear bands are initially formed at the upper yield point. Development of the bands is accompanied by a drop in the stress to a lower yield point. At the lower yield point the strain inside the bands is approximately 70% and remains constant thereafter. Further deformation occurs by growth of the bands until they cover the entire sample. When the direction of twisting is reversed after the shear bands are formed, the deformed material untwists uniformly, without deformation in the previously undeformed material, and the stress required for untwisting the deformed material is lower than the stress required to propagate the band into undeformed material.
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  • 91
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2253-2260 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Cloud-point curves and relative volumes of the coexisting phases just below the cloud-point temperatures were observed for a commercial sample of “monodisperse” polystyrene and one of its fractions. As expected from theoretical considerations, the cloud-point curve for the more monodisperse sample was flatter near the peak over a greater concentration range than that of the parent sample. Furthermore, the critical point for the fraction appeared to be closer to the peak of the cloud-point curve than was that of the unfractionated polymer. In addition, it was learned that one type of impurity could be detected with extraordinary sensitivity by means of the cloud-point curve.
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  • 92
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2273-2282 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The relevance of diamagnetic susceptibility as a tool for the structure analysis of solid high polymers is stressed in the light of some new examples. The present results complement previous data and offer new aspects on the diamagnetic investigations of longchain hydrocarbons, especially polyethylene (PE). The molecular susceptibility is proportional to the average number of repeat units in the chain. The proportionality factor defines an intermolecular constant μk which characterizes different physical states. This was found to be 2.5 × 10-6 for the liquid and 3.5 × 10-6 cgs for the crystalline state of paraffins and polyethylene (solution-crystallized). For melt-crystallized material, μk, approaches the typical value of the liquid paraffin in agreement with previous results. Such a low μk is probably related to the increased disorder of the paracrystalline lattice domains, in contrast to the more ordered microparacrystallites in the so-called “single crystals,” where μk = 3.5 × 10-6. In single crystals of branched PE, μk approaches 2.5 × 10-6 with increasing branching ratio. Like paraffins in the gaseous state, molten PE, with chains longer than 1000 Å, has μk = 0. If the solution-crystallized material is molten for 10 min and thereafter cooled, μk retains the original value 3.5 × 10-6 cgs characteristic of the crystalline state. Hence, solution-crystallized polyethylene apparently possesses a kind of “memory.” Such a “memory” can, nevertheless, be partly destroyed when molten PE is stirred for 10 min and then quenched. Aggregates of solution-precipitated crystals with 3% branching concentration give μk = 2.9 ± 0.2 × 10-6 in good agreement with x-ray diffraction data. Finally, experimental details on the magnetic measurements are critically discussed, and various aspects of improvements for further investigations are also described.
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  • 93
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 991-1003 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Determination of important thermodynamic and physical properties of polymers has often been frustrated by the tendency of these materials to reorganize when heated. A novel technique has been developed which permits a more careful examination of the relationships existing between melting and morphology of single crystals. This has lead to the observation that high molecular weight polymers possess much narrower melting ranges than had been previously reported. By using this technique it has been possible to identify distinct transition temperatures for {100} and {110} fold sectors. DTA and DSC data have been previously reported for dried down single crystals. The applicability of this data to single crystals as they exist in suspension is questioned.
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  • 94
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 973-989 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Injection-molded specimens of polypropylene were examined by x-ray diffraction for texture and orientation patterns as a function of the distance from the surface and of molding conditions. At least three distinct layers in the surface region whose texture patterns differ and an isotropic core of the moldings have been identified. These layers show preferred orientations; the axes of symmetry of the oriented textures lie in a plane passing through the direction of flow and perpendicular to the mold surface, but are inclined to the mold surface at a small angle. Some of these layers may be missing in conditions of either very high or very low shear during the injection-molding flow. A tentative explanation of the formation of the texture patterns is proposed.
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  • 95
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1111-1116 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The polymerization of p-xylylene was followed with a newly designed differential thermal analysis system at temperatures between -196°C and -20°C. It was found that at the lower temperatures the monomer condenses first to the crystalline monomer before simultaneous polymerization and crystallization. At the higher temperatures, polymerization and crystallization are successive. The data are in agreement with the morphology and crystal structure data derived in Part I of this series of papers on crystallization during polymerization of poly-p-xylylene.
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  • 96
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1151-1171 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(p-phenylene pyromellitamic acid)s were synthesized over the weight-average molecular weight range 8,000 to 22,000. The polymers were recovered as amorphous powders composed of 3-4 × 1-2 μ platelets 0.1-0.2 μ thick containing 20-30% associated solvent. Consumption of reactants and attainment of the ultimate molecular weight of the polymer were found to occur within the first few minutes of reaction. The polymers were characterized by scanning electron microscopy; ultraviolet, visible, near-infrared, and infrared spectroscopy; x-ray analysis; viscometry; and light-scattering photometry. The intrinsic viscosity-molecular weight relation for the polymer in DMF was \documentclass{article}\pagestyle{empty}\begin{document}$ [\eta ] = 25.2 \times 10^{ - 4} \bar M_w^{0.56} $\end{document}.
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  • 97
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1139-1150 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The hydrodynamic volume concept can be used effectively with gel-permeation chromatographic (GPC) and viscosity data to estimate the molecular weight of a variety of polymers. Agreement is within ±5-10% of the absolute values and thus is satisfactory for many purposes. An iterative computer technique and a method developed by Funt and Hornof for analyzing GPC-viscosity data were found to be equivalent with respect to estimating the molecular weights for the five cases studied. The latter is easily employed but restricted to the case where the sample of interest and the GPC calibration standards have approximately equal Mark-Houwink parameters. Since GPC measurements are commonly performed in thermodynamically good solvents, the general applicability of the method is not impaired. Using the unperturbed dimensions of the polymer chain to estimate the molecular weight of a variety of polymers was not as satisfactory as the above techniques. This approach generally gave biased molecular weight values (consistently low or consistently high). Agreement with the absolute values ranged from 10 to 30%. We therefore believe that either of the techniques based on the hydrodynamic volume concept can be used more effectively to estimate the molecular weight of a series of polymers than the treatment based on the unperturbed dimension.
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  • 98
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Polarized lower-frequency infrared spectra (800-33 cm-1) of nylon 66 (α form), nylon 77 (γ form), and nylon 6 (both α and γ form) have been examined. The spectral changes which occur on complex formation of the polyamides with iodine-potassium iodide solution and on subsequent iodine desorption have been studied in relation to the changes in the polymer structures. On the basis of these results, most of the stronger bands have been reasonably assigned to the vibrations characteristic of the amide group and the methylene chain of the polyamides, and some new structure-frequency correlations have been established for the polymers.
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  • 99
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1271-1284 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The low-strain-rate tensile stress-strain properties of cis- and trans-polybutadienes and -polyisoprenes, polybutadiene (cis/trans/vinyl), butyl rubber, and two SBR copolymers have been investigated from 77°K to up to 25°K below the glass transition temperature Tg. The energy Ep dissipated in a stress-strain test in the region of previously reported secondary glass transitions is found to be a function of both the free volume f̄Tg at the Tg and the damping A4Tg from 4°K to Tg -25°K. The complex relationship between the impact strength, the free volume and the damping is briefly discussed. The effect of quenching through the Tg with liquid nitrogen was found to increase the value of Ep for all materials. In a number of cases this increase was associated with the presence of internal crazes. The surface-craze initiation stress is increased by the presence of surface residual compressive stresses caused by quenching. The internal tensile stresses balancing the surface compressive stresses together with the applied tensile stress cause internal dilatation and hence preferential initiation of internal crazing.
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  • 100
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1477-1488 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The isothermal crystallization of natural rubber was investigated under biaxial stretching. A marked planar orientation of crystals occurs in such a way that the (010) plane orients parallel to the film plane. The rate of crystallization increases with the biaxial stretching ratio, and the Avrami exponent n decreases. At the highest extension, n becomes less than unity. The equilibrium degree of crystallinity decreases with the stretching ratio. The crystallinity was less than 10% for the highest extension. The melting behavior is similar to that in uniaxial stretching.
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