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  • Physics  (2,549)
  • 1970-1974  (2,547)
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  • 101
    Electronic Resource
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1617-1626 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The swelling curves of 6μ films of low conversion homopolymers and copolymers of acrylamide (AM) and N-isopropylacrylamide (NIPAM) were obtained in water by an optical microscope technique. Poly(AM) swelled appreciably faster than poly(NIPAM) but there was no apparent correlation between overall swelling rate and copolymer composition. A 57/43 (mole %) AM-NIPAM copolymer swelled fastest. Sequence distribution calculations indicated that its backbone structure tended toward comonomer alternation, which might reduce the extent of hydrogen bonding in the film. The amount of water sorbed during swelling, as approximated from increasing film thickness, was proportional to the square root of time and agreed well with previous work in the literature. Homopolymer films from runs of ca. 50% conversion consistently swelled slower than their low conversion counterparts, probably due to branching and increased entanglements. Heating also promoted slower film swelling due to a tightening of the film structure and/or a low degree of imidization. Monomer reactivity ratios and Alfrey-Price Q and e values for NIPAM were calculated. Cloud points of 5% aqueous solutions of the copolymers were measured and found to decrease with increasing NIPAM content.
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  • 102
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1637-1637 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 103
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    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1661-1678 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The orientation of crystals in spherulites of modifications I and II of polybutene-1 was studied by micro-x-ray diffraction. Changes in such micro-x-ray diffraction patterns were measured in various regions of the spherulites as a function of strain and time. The relationship between micro-x-ray diffraction from parts of spherulites and macro-x-ray diffraction from entire spherulites is discussed. Changes are resolved into contributions arising from (1) deformation of spherulites with change in crystal orientation and (2) transformation of crystals from modification II to modification I.
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  • 104
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystal structure of nylon 3 was studied, and four crystalline modifications were observed. Modification I, as determined from the x-ray diffraction pattern of drawn fibers, is similar to the α crystal structure of nylon 6. The unit cell is monoclinic; a = 9.33 Å, b = 4.78 Å, (fiber identity period), c = 8.73 Å, and β = 60°. The theoretical density for nylon 3 with four monomeric units in the unit cell is 1.39 g/cm3, and the observed density is 1.33 g/cm3. The space group is P21. The nylon 3 chains are in the extended planar zigzag conformation. Although other odd-numbered nylon form triclinic or pseudohexagonal crystals when oriented, drawn nylon 3 crystals are monoclinic. In addition to modification I, modifications II, III, and IV were studied. Lattice spacings of modifications II and III are equal to those of modification I. However x-ray diffraction intensities are different. Infrared spectra of those forms indicate an extended planar zigzag conformation of the chains. Modification IV is thought to correspond to the so-called smectic hexagonal form. No γ crystals were found, and it appears that polyamide chains with short sequences of methylene groups cannot form crystals of this type.
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  • 105
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    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 991-998 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The diffusion of 1,1-diphenylethane in trace amounts through eight rubbery polymers has been studied by radioactive tagging of this penetrant with 14C. For several polymers, the dependence on temperature and on dilution (swelling) by untagged diphenylethane was investigated. In the diluted systems, tagged n-hexadecane was also used as a trace penetrant. The temperature and concentration dependences were interpreted rather successfully in terms of the free volume. In comparing different polymers, with a 4000-fold range of diffusion coefficients, the translatory friction coefficient of 1,1-diphenylethane was found to be proportional to that of n-hexadecane to the power 1.06. This is interpreted qualitatively by the free volume concept to indicate a slightly less efficient mobility mechanism for the diphenylethane.
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  • 106
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    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1415-1424 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The mutual diffusion of pairs of polymers has been studied at 160°C for two systems: isotactic polypropylene with polyethylene and poly(vinyl chloride) with polyethylene. From the assumption that Fick's law is valid and with a rhombohedral lattice model for the microheterogeneous system, it was possible to obtain from volume changes the thickness of the interphase layer after various diffusion times. It was found that the values so calculated differ considerably from the experimental values, the greatest deviations occuring after 20 min diffusion. From this it follows that non-Fickian diffusion strongly influences the distribution of concentrations in the diffuse interface, and thus affects the calculated value of the interphase layer thickness. For both polymer pairs Fickian behavior was confirmed for up to about 10 min diffusion time, in good agreement with experimental data.
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  • 107
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    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1503-1519 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A statistical theory for the scattering of light from oriented polymer films is developed in terms of angularly dependent generalized correlation functions. Numerical calculations of scattering patterns are carried out for special cases. The scattering depends upon two types of distributions describing (1) the orientation distribution of optical axes of scattering elements and (2) the angular dependence of correlation in orientation between pairs of optic axes. These distributions are expanded in Fourier series (in a two-dimensional treatment), the coefficients of which are functions of elongation and describe the elongation dependence of the scattering patterns.
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  • 108
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    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1845-1845 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 109
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    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1885-1896 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new light scattering photometer has been designed in order to perform light-scattering measurements at various temperatures and under pressures of 1-1000 atm. Since the scattering angle is constant (90°C), the dimensions of the dissolved molecules are determined by measuring the intensity at different wavelengths. The method of measurement, the calibration of the instrument, and the treatment of data are described. By a series of test measurements on polystyrene in trans-decalin solutions it is shown that one obtains reliable results and finds considerable effects of pressure on the radius of gyration and the fundamental thermodynamic properties of the system.
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  • 110
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Insertion poly(methyl methacrylate) (PMMA) formed within a monolayer of monomer adsorbed on montmorillonite was studied by means of NMR spectroscopy and shown to be composed of short stereosequences with a predominant isotactic component. The stereospecificity of the insertion PMMA can be understood in terms of the organization of the monomer adsorbed on the surface of the mineral. The monolayer of monomer is assumed to be composed of monads and isotactic diads due to dipole-ion interactions between the molecules of methyl methacrylate and exchangeable cations. Results of experiments relating factors such as temperature, density of ion population of the surface, and the nature of ions are discussed. It is shown that the populations of isotactic and syndiotactic triads Pi and Ps determined experimentally in the insertion PMMA are in a reasonable agreement with values calculated from the model. It is shown, furthermore, that Pi increases with increase in the density of the ion population, in agreement with the equations derived from the model.
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  • 111
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    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1637-1637 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 112
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    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1443-1456 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of varying molecular weight distribution on the self-seeding phenomenon was investigated by using high molecular weight polyethylene fractions prepared by the stirring-induced crystallization method of Pennings. The numbers of self-seeding nuclei per gram were determined by measuring crystal dimensions, and were found to increase with increasing molecular weight of the polymer, in accord with previous findings. In another experiment, self-seeded single crystals were grown from materials of various molecular weights, prepared by blending two samples of differing molecular weight in various proportions. The concentration of nuclei varies linearly with the weight fraction of high molecular weight polymer in the mixture. This result is shown to be consistent with the proposition that each nucleus contains on the average an identical number (most plausibly one) of molecules of very high molecular weight. The application of this finding to the determination of molecular weights is discussed, and it is shown that the technique provides a method of unprecedented sensitivity for the characterization of the very high end of the molecular weight spectrum. Some morphological results are also presented. In particular, direct observations of the nuclei were found to be consistent with the loosely connected multiple nucleus structure, which had been proposed previously to account for certain light-scattering results.
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  • 113
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    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1575-1584 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The resonance frequencies of unidirectional carbon fiber reinforced/epoxy composite beams were studied over the temperature range 24-225°C. Longitudinal Young's moduli E11 and longitudinal-transverse shear moduli G12 were computed from the experimental data by the use of Timoshenko beam theory. The effects of transverse shear deformation (a function of E11/G12) were found to increase in importance with increasing temperature. Values of G12 were found to be approximately proportional to the shear modulus Gm of matrix material but were about 30% lower than predicted by the theory of Hashin and Rosen. The anisotropy of the carbon filaments and voids in the composite samples were proposed to account for the discrepancy between theory and experiment.
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  • 114
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    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1635-1635 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 115
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    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1639-1649 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The general problems presented by the determination of the optical activity of polymers in the crystalline state are considered. The necessity of using unoriented samples, if the polarimetric data are to be compared with analogous data measured in solution, is emphasized. The optical activity in the crystalline state of a number of stereoregular vinyl polymers has been measured by employing either suspensions of fine powders or thin plates with no detectable orientation. The results of optical rotatory dispersion studies in the crystalline state suggest that, at least in the case of the poly-α-olefins investigated, the same chromophores are responsible for the optical activity in the crystalline state and in solution.
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  • 116
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    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1697-1701 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Middle range fractions of mimusops balata, a natural trans-1,4-polyisoprene, exhibit transcrystallinity when crystallized in the 35-40°C range. The presence of transcrystallinity was established by x-ray diffraction and optical microscopy. Diffraction peak intensities change due to transcrystallinity, suggesting x-rays be used to detect transcrystallinity and that caution be exercised in using x-ray diffraction techniques to determine the phases present in bulk material and in calculating the degree of crystallinity. The tendency toward transcrystallinity may depend upon molecular weight.
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  • 117
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    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1723-1740 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The transformation of microspherulitic quenched and annealed polyethylene film into highly oriented drawn material with the characteristic fiber structure was investigated by small-angle and wide-angle x-ray measurements and by a study of the thermograms after the fuming nitric acid treatment. With the details of deformation depending slightly on the crystallinity, one observes generally a preferential tilt of the platelets against draw direction at draw ratios below 2. At least in annealed material, an increasing tilt of the molecule within the lamella is also observed, which leads at higher draw ratios to slipping of blocks in the crystallites. With further drawing a new fiber structure appears, which is practically independent of the thermal history of the original film. This fact is established by investigation of the crystal thickness by three different methods; investigations of small-angle scattering, study of the width of the (002) reflection, and investigation of the debris after treatment with fuming nitric acid.
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  • 118
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 543-555 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Photocurrents developed in polyethylene in the wavelength range 360-180 nm have been measured. The action spectra show features which can be related to the corresponding features in the absorption spectrum, and in addition there is electron injection from the metal electrode at a wavelength determined by the electrode material. The time dependence of the response indicates that a long-lived space charge is formed in the material.
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  • 119
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 569-576 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Large photocurrents have been observed in films of some simple polymers (containing no π-orbitals), of which poly(vinyl fluoride) is a typical example. Not only are the currents large (up to 10-5 A/cm2) but also they are capable of being excited by light in the visible wavelength region where absorption by the polymer is too low to be detectable. The results indicate that the effects are electronic, rather than ionic, in nature.
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  • 120
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 577-584 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It was previously shown that for a stationary random copolymer of A, B, and C, we have in general p(AB) + p(AC) = p(BA) + p(CA), etc., in place of p(AB) = p(BA) which is valid for a stationary binary copolymer. Here, p(AB) for example, is the probability that a randomly picked pair of consecutive comonomers in the polymer consists of an A followed by a B. For a stationary ternary copolymer produced by a first-order Markovian addition mechanism, we show that PABPBCPCA/PACPCBPBA = k, where k is a constant characteristic of a particular set of three monomers but independent of its composition. Here, PAB is the conditional probability of finding a monomer of B given that its immediate predecessor is an A. We further show that if the individual rate constants of the monomer additions involved take a special form such as used in the Alfrey-Price Q-e scheme, then we have k = 1 irrespective of the kinds of monomers, and in addition we have p(AB) = p(BA), p(AC) = p(CA), etc. Thus, although these latter results were previously proposed by Ham as an alternative basis to supplant the Q-e scheme, they may rather be regarded as mathematical consequences of special assumptions adopted for the form of the individual rate constants. For a stationary random copolymer of four components A, B, C, and D, we have p(AB) + p(AC) + p(AD) = p(BA) + p(CA) + p(DA), etc., in general. For a first-order Markovian four-component copolymer, we show that there are seven different combinations of the conditional probabilities that are constants (k1, k2,…, k1) independent of the monomer composition. Again, if we assume the same special form for the rate constants involved, we find that all the seven constants k1, k2, …, k7 reduce to unity and p(XY) = p(YX) for X,Y, = A, B, C, D.
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  • 121
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 717-729 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Several copolymers as well as homopolymers of vinylidene chloride and vinyl chloride have been examined by Raman spectroscopy. Probabilities of concentrations of monomer sequences have been calculated from known reactivity ratios. Surface scattering intensities at some frequencies were found to be linearly proportional to specific microstructure concentrations. Normalization of scattering intensities was accomplished using the intensity of the CH2 asymmetric stretching mode at 2926 cm-1, which is common to all samples examined. Good correlation was found for the concentrations of comonomer sequences {B}, {BB}, {BBB}, {AA} and {AAAA} in which A denotes vinylidene chloride and B vinyl chloride.
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  • 122
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 755-758 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The mass flux entering the Fick's diffusion equation is considered as an arbitrary analytical function of concentration, concentration gradient, and of the gradient of concentration gradient. The restrictions imposed on the flux by the principle of material objectivity are stated and briefly discussed.
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  • 123
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 759-762 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 124
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1287-1303 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The viscoelasticity and volume expansion of the raw polymerizate of ethylene-propylene copolymer with vinyl chloride grafts, and of the individual components has been studied. The raw polymerizate (composite) and the pure ethylene-propylene-vinyl chloride graft copolymer were found to consist of two phases. The pure graft copolymer has an ethylene-propylene matrix containing some fraction of poly(vinyl chloride) (PVC) grafts and a microphase with the remainder of the PVC grafts. The raw polymerizate consists of a PVC matrix plasticized with ethylene-propylene chains and a microphase of the ethylene-propylene copolymer. An attempt has been made to calculate the participation of components in microphases and the minimum dimension of the PVC microphase aggregates.
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  • 125
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1333-1339 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The lattice-theory equations for the surface tension of polymer solutions based on the parallel-layer model have been extended to include more than two components. The surface tensions of tetrachloroethylene solutions of some blended polydimethylsiloxane fluids have been measured at room temperature. The results are in nearly quantitative agreement with the theoretical calculations.
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  • 126
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1371-1378 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new relaxation process, explaining the change of elasticity in rubberlike polymers at critical stress (0.1-0.5 kgf/cm2) has been discovered. This process is characterized by the low value of activation energy (weak temperature dependence of relaxation times) and large sizes of kinetic units (strong dependence of relaxation time on stress). Critical stress depend on temperature and for rubberlike polymers turns to zero at 40°-60°C. Mechanism of the phenomena can be explained by the existence of the ordered molecular microregions, creating additional crosslinking points of nonchemical nature with free chains of the network, breaking up at critical stress. Observed phenomena is analogous to the process of forced rubber elasticity of those polymers in glassy state. Critical stress is analogous to the limit of forced rubber elasticity below glass transition temperature.
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  • 127
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1449-1469 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Wide-line NMR spectra have been obtained on an oriented sample of drawn nylon 66 fibers at temperatures between -196°C and 200°C and at alignment angles between the fiber axis and the magnetic field of 0°, 45°, and 90°. At -196°C, 20°C, and 180°C, the complete angle dependence of the NMR spectrum has been measured. The second moments of these spectra have been compared to theoretical second moments calculated for various models of chain segmental motion in an attempt to elucidate the mechanisms involved in the low-temperature segmental motion (γ process) and the high-temperature segmental motion (αc process). In agreement with earlier suggestions, the present results indicate that the γ process consists of segmental motion in noncrystalline regions. The overall decrease in second moment caused by the γ process is consistent with a model in which all noncrystalline segments rotate around axes nearly fixed in space. Furthermore, this decrease shows a pronounced dependence on the alignment angle. It is believed that this is due to tie molecules which become highly oriented along the fiber axis during drawing; their axes of rotation will therefore be nearly parallel to the fiber axis. The segments in noncrystalline entities such as chain folds and chain ends are less well oriented along the fiber axis and make an essentially isotropic contribution to the second moment decrease. The second moment at 180°C indicates the presence of considerable motion in the crystalline regions, and this motion is denoted the αc process. The second moment Sc of the crystalline regions is strongly dependent on the alignment angle, the predominant feature being a relatively high value of the second moment when the fiber axis is directed parallel to the magnetic field. This is in qualitative, but not quantitative, agreement with the motional model recently advanced by McMahon, which assumes full rotation of the chains around their axes. Excellent quantitative agreement with experiment has been obtained by superimposition of rotational oscillation around the chain axis of amplitude roughtly 50°, and torsion of the chains with neighboring CH2 groups oscillating around the C—C bond with a relative amplitude of about 40°. A model in which the chains perform rotational jumps of 60° between two equilibrium sites has also been considered (60° flip-flop motion). A distinction between this model and rotational oscillation has not been possible.
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  • 128
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1525-1529 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 129
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1553-1577 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: As is well known, the chemical potentials of polymer and solvent in solution and, hence, the Flory-Huggins interaction parameter χ can be determined from scattered light intensities from dilute and concentrated solutions of the polymer in the solvent concerned. Preferably, measurements should be performed at temperatures as low as possible, provided the temperature exceeds the cloudpoint for the concentration used. It is shown that the lower the temperature and, consequently the higher the scattered light intensity, the better is the accuracy of the parameters obtained. At each temperature the scattered light intensity shows a maximum at some concentration. Below the theta temperature the ratio of scattered light intensity and concentrations also shows a maximum at some concentration. The values and the concentrations of these maxima for various temperatures enable the maximum of the spinodal to be determined. The spinodal itself can be determined by an extrapolation procedure of the reciprocal scattered light intensities. Measurements have been performed with three narrow-distribution polystyrene samples in cyclohexane. On the basis of the results, χ, and its dependence on concentration, temperature, and molecular weight can be determined to high accuracy.
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  • 130
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1641-1655 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The morphology of high-density polyethylene crystallized under simultaneous pressure and shear in an Instron capillary viscometer has been examined by scanning electron microscopy, electron microscopy, and selected-area electron diffraction. Two distinct fibrous morphologies were observed in these unusually transparent strands. The outer sheath was composed of fibers, 3000 Å in diameter, aligned parallel to the extrusion direction and apparently interconnected by a lamellar cross texture. A highly crystalline ribbon texture composed of fine fibers, 200-250 Å in diameter, dominated the inner core. Sharp-spot electron diffraction patterns obtained from these central ribbons indicated a high degree of c-axis orientation parallel to the fibers and an extended-chain crystal structure. The melting behavior of both irradiated and unirradiated strands examined by differential scanning calorimetry was consistent with the formation of two distinct crystalline morphological units.
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  • 131
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1681-1691 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The influence of the nature of exchangeable cations on the tacticity of poly(methyl methacrylate) (PMMA) prepared from montmorillonite-MMA adsorption complexes was investigated. The strength of ion-dipole interactions was estimated either by the value of the electrostatic interaction potential or by the value of the carbonyl-stretching frequency shift. It was shown that Pi, the percentage of isotactic triads in the polymer, increases with increasing strength of the ion-dipole interactions, while the persistence ratio and the mean length of closed isotactic (or syndiotactic) sequences remain essentially unchanged regardless of the nature of the cation. It was shown that values of Pi may vary from 0.15 for weakly interacting ions to 0.5 for strongly interacting ones, reaching at the upper limit the value calculated from the model proposed in a previous paper, thus confirming its validity.
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  • 132
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1693-1702 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Differential thermal analysis (DTA) of some commercial nylons has disclosed some anomalous phenomena with respect to the glass transition, generally considered to occur at 40-50°C. On the first heat cycle the transition occurs normally. On cooling, however, no corresponding transition occurs, and on an immediate rerun the transition has disappeared. If another DTA thermogram is made after a few hours, the transition begins to reappear, but at a temperature lower by a few degrees. After about five days rest, the transition is again normal in size and temperature. On annealing at 75°C, the 43°C transition is pushed up to about 92°C. On resting after annealing, transitions appear at both 40 and 92°C. These phenomena are explained in terms of the slow formation of a hydrogen-bonded network in the amorphous regions of the polymer. It is the disruption of this network that is normally considered to be the glass transition in nylons. The network is slow in re-forming because of problems involved in matching up potential hydrogen-bonding sites, which are, of course, distributed at intervals along the polymer chain. The temperature at which the network is disrupted is apparently dependent not so much on the ratio of bonding to nonbonding sites, as on the temperature at which it was formed.
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  • 133
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1793-1805 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Detailed critical examinations of three aspects of nitric acid treatment of polyethylene are reported. (1) The endgroups introduced by the nitric acid are examined. It is concluded that in samples degraded to a single-crystal traverse stage, carboxyl features only as endgroup, and conversely each chain-end is terminated by such a group. Consequently, the carboxyl content can be used for quantitative characterization of the cut chain length. The function and position of the nitro group remains unexplained. (2) The morphological selectivity of the nitric acid-induced degradation is scrutinized. It is concluded that the crystal core is attacked and thinned by the acid; the slowing down of the reaction is principally due to accumulation of reaction products. Accordingly, the usual distinction between a vulnerable amorphous layer and a resistant crystal core is not justified on the basis of such degradation experiments. It follows that meaningful structural information is obtained only when the relevant crystal properties are studied as a function of chain cutting, assessed from the molecular weight distribution (GPC), as opposed to that of degradation time alone. (3) The role of sample consistency and reagent strength has been examined. It is demonstrated that for the reaction to be sufficiently uniform throughout the sample for the results to be meaningful, the reaction rate has to be slow compared to the rate at which the reagent diffuses into the specimen. To realize these conditions, finely dispersed samples and weak reagents were found to be favorable
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  • 134
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1871-1885 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Several samples of a copolymer were examined by means of equilibrium centrifugation in a density gradient. The results for the samples without compositional distribution (homogeneous polymers) were used to determine the relation between the chemical composition and the distance from the center of rotation. For one of the homogeneous polymers a quantitative analysis of the schlieren curve was made in order to show the kind of accuracy that can be achieved. For the inhomogeneous polymer it was found that the schlieren curve could, in principle, be described quantitatively by the assumption that fluctuations in composition are independent of fluctuations in molecular weight, but on this basis the average square of the fluctuations in composition is more than four times smaller than the value derived from chromatographic data. A more satisfactory explanation of the experimental results is provided by assuming a linear correlation between average molecular weight and composition, but it is not claimed that this is necessarily the only model that explains the data.
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  • 135
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1887-1905 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Time-dependent, apparent heat capacities of glucose, poly(vinyl chloride), polystyrene, selenium, poly(methyl methacrylate), and poly(2,6-dimethyl-1,4-phenylene ether) in the glass transition region were determined by differential thermal analysis. The thermal history was set by linear cooling at rates between 0.007 and 160°C/min. Linear heating for analysis was carried out at rates between 0.3 and 600°C/min. Average activation energies of 52, 81, 90, 54, 77, and 108 kcal/mole, respectively, were evaluated by using the hole theory of glasses previously developed. Within experimental limitations all data could be described quantitatively by the theoretical expressions using only one parameter, the number of frozen-in holes, to described the thermal history. Experimental and theoretical limitations are discussed.
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1915-1918 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology , Physics
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  • 137
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    Notes: A mathematical development interrelating the orientation distribution functions of three kinds of orientation units for a polymer spherulite (i.e., a crystal lamella, a crystallite, and a given reciprocal lattice vector of the crystallite) is formulated on the basis of series expansions of the distribution functions in generalized spherical harmonies. Two types of uniaxial deformation models of a polyethylene spherulite, taking account of micronecking and untwisting of crystal lamellae, and of chain tilting and untwisting of crystal lamellae, respectively, both in addition to affine deformation of the lamellae are discussed. The models are tested by comparison of the theoretical orientation distribution functions of some reciprocal lattice vectors of the crystallite with the results of x-ray diffraction experiments.
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2033-2042 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Wide-line NMR spectra of nylon 66 fibers have been obtained at different alignment angles between the fiber axis and the magnetic field, at varying water contents (H2O and D2O), and at different temperatures. At 28°C the spectrum of the dry fibers consists of a nearly structureless broad line. At water regains of 1.4% by weight (dry basis) and higher a sharp line appears which originates from highly mobile water molecules. The width of this line decreases with increasing water content, implying an increase of water mobility. Moreover, the width is a function of the alignment angle; this shows that the water is not reorienting isotropically owing to specific water-polymer interaction. The amount of mobile water is always smaller than the amount of water absorbed. At water contents close to saturation, a mobile polymer line appears with a width intermediate between the broad line (immobile polymer) and the sharp water line. This line, most clearly observed at an alignment angle of 0°, is due to a shift of the αa process to lower temperatures in the presence of water. A similar line is observed in the dry fibers at 120°C. It is shown that the αa process decreases the NMR second moment only slightly. The shift of the high temperature drop in second moment to lower temperatures in the presence of water is therefore interpreted as due to a shift of the αc process, and not of the αa process, to lower temperatures.
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2099-2103 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2119-2130 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A general theory of non-Gaussian elasticity is presented for real polymeric chains having fixed bond angles and restricted internal rotations. The theory contains the displacement-vector distribution given by Nagai, and the Flory-Wall-Hermans procedure is used for the calculation of network properties. Whereas the treatment is valid for all types of polymer chains, it is not totally satisfactory from a practical standpoint because of a slow series convergence if the chains are stiff. It is best utilized for flexible polymers under conditions of light crosslinking. Detailed network behavior is investigated only for polyethylene type chains having uncorrelated internal rotations. In this instance the fractional contribution fe/f of the internal energy of the total force f is found to be a function of elongation at high degress of stretching. It may decrease, or increase, depending upon the sign of fe/f at low elongations. Furthermore, the variation of fe/f with elongation is independent of the fixed bond angle of the chain backbone. Stress-strain behavior and energy-strain behavior are in opposition, i.e., when the non-Gaussian contribution to the stress is greatest, it is the least for the ratio fe/f, and vice versa. The presence of correlated internal rotations would not be expected to greatly alter these general conclusions.
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2247-2251 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology , Physics
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1-9 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology , Physics
    Notes: It has been shown in this investigation that the permeation of propane and propylene through polyethylene membranes exhibit a generalized behavior in the vicinity of the condensation point of the penetrant. Correlations to evaluate the permeation flux are presented.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 43-50 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Natural rubber crosslinked by dicumyl peroxide in amounts up to 25 parts per hundred of rubber (phr) showed a maximum in tensile strength near 1 phr, followed by a steep decrease to a minimum near 5 phr. The ultimate elongation decreased from 870% at 0.5 phr. to about 10% above 10 phr. The modulus increased linearly with increase of crosslinking. The creep rate decreased from 5.6% per decade at 0.5 phr to zero at 5 phr and higher values. Crystallization, with a resultant abrupt increase in creep, was noted in specimens held in the stretched condition for more than one day. Between 5 and 25 phr this system (when crystallization is avoided) appears to function as an ideal elastic network and can be recommended for studies of rubber elasticity since no variation of modulus with time is observed.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 151-157 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The problem of the segregation of subchains in an isolated molecule of an A-B block copolymer is closely related to that of the mutually excluded volume of two chemically differing macromolecules. Therefore, by resorting to the “segment cloud” model used by Flory and Krigbaum to calculate the excluded volume, it was possible to derive an expression for the number of contacts between the two blocks in the same molecule. From the results of the calculation it follows that only partial block segregation can be expected unless the condensation of one of the subcoils to a dense globule occurs, owing to the effect of a poor solvent quality.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 171-189 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The concentration dependence of the reduced viscosity of a number of polyelectrolytes was found to be adequately described by the equation \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm \eta }_{sp} /c = [{\rm \eta }]_\infty [1 + k/\sqrt c ] $\end{document} as long as the concentration is not too low. The parameter [η]∞ represents the intrinsic viscosity of the well-shielded polyion and corresponds to values of [η] determined in salt solutions and may possibly correspond to the theory of Harris and Rice on polyion expansion. Heuristic arguments based in part on the work of Katchalsky et al. lead to a definite expression for the parameter k in terms of molecular properties. This result shows that the above equation is valid only for strong polyelectrolytes with constant activity coefficients of counterion. The calculated values of k agree well with experiment except when specific intramolecular interactions (e.g., internal hydrogen bonding) occur. For highly charged polyions we find, surprisingly, that k depends only on the properties of the polymer backbone and not on electrical properties.
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  • 146
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    Notes: Ten unfractionated poly(2,6-diphenyl-1,4-phenylene oxide) samples were examined by gel permeation chromatography (GPC) and intrinsic viscosity [η] at 50°C in benzene, by intrinsic viscosity at 25°C in chloroform, and by light scattering at 30°C in chloroform. The GPC column was calibrated with ten narrow-distribution polystyrenes and styrene monomer to yield a “universal” relation of log ([η]M) versus elution volume. GPC-average molecular weights, defined as M̄gpc = \documentclass{article}\pagestyle{empty}\begin{document}$\Sigma w_i [\eta ]_i M_i /\Sigma w_i [\eta ]_i$\end{document}, wi denoting the weight fraction of polymer of molecular weight Mi, were computed from the GPC and [η] data on the polyethers. The M̄GPC were then compared with the weight-average M̄w from light scattering. The intrinsic viscosity (dl/g) versus molecular weight relations for the unfractionated poly(2,6-diphenyl-1,4-phenylene oxides) determined over the molecular weight range 14,000 ≤ M̄w ≤ 1,145,000 are log [η] = -3.494 + 0.609 log M̄w (chloroform, 25°C) and log [η] = -3.705 + 0.638 log M̄w (benzene, 50°C). The M̄w(GPC)/M̄n(GPC) ratios for the polymers in the molecular weight range 14,000 ≤ M̄w ≤ 123,000 approximate 1.5 according to computer integrations of the GPC curves with the use of the “universal” calibration and the measured log [η] versus log M̄w relation. The higher molecular weight polymers (326,000 ≤ M̄w ≤ 1,145,000) show slightly broadened distributions.
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  • 147
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    Notes: The crystallization and melting temperatures of an unfractionated poly(2,6-dimethyl 1,4-phenylene oxide) (PPO) sample, PM2, were determined at 0.25°C/min cooling and heating rates in five binary toluene - PM2 and fifteen ternary toluene - polystyrene - PM2 solutions. The total polymer weight fraction range studied was 0.12-0.40 and the PM2 weight fraction range was 0.026-0.40. The heat of fusion Hf of the PM2 was computed to be 10.1 cal/g from the melting point depressions. A toluene - PM2 pair interaction parameter χ13 = 0.890 - 223.5/T was found. Although a reliable polystyrene-PM2 interaction parameter could not be computed, the data are consistent with χ23 = 0. Setting χ23 = 0 we calculate the toluene - polystyrene interaction parameter to be χ12 = 0.495 - 15.46/T. This χ12 is in remarkable agreement with values reported in osmotic pressure studies.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 381-384 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 385-432 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Anisotropic growth of β-form crystals of isotactic polypropylene in type III and type IV spherulites has made possible microanalysis of the unit cell structure, optical properties, and crystal arrangement within the spherulites. Micro x-ray studies of the type III and type IV spherulites show that interspherulitic β-form crystals have a hexagonal unit cell with dimensions; a = 19.08 Å and c = 6.49 Å. The intrinsic refractive indices of these β-form crystals are 1.506 along the a axis and 1.536 along the c axis. The organization of the crystals within the spherulites and the optical properties of the spherulites are also quantitatively evaluated. Both the type III and type IV spherulites have the a axis of the crystal radial while the crystals rotate randomly around the type III spherulite radii and periodically around the type IV spherulite radii. The radial refractive index for both the type III and type IV spherulites has the same value of 1.496. The tangential refractive index of the type III spherulite has a constant value of 1.509; it varies periodically between a minimum of 1.496 and a maximum of 1.519 in the type IV spherulite. Microtechniques such as micro x-ray diffraction, interference microscopy, birefringence, and optical microscopy were required for acquisition of the data.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 541-548 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The tack of cis-polybutadiene was measured by means of a Skewis tackmeter, and the results, which showed considerable variability, could be represented by a double exponential cumulative distribution function of Gumbel. It was concluded that there exists a linear relationship between the applied forces (contact and break) and the time that these forces are applied in the tack test. The mechanism of tack is considered in terms of two distinct processes: (a) the development of a bond and (b) the strength of the bond thus formed. The latter is rationalized by applying Eyring's absolute rate theory. A simple equation is derived which predicts an inverse linear relation between the breaking time and breaking force, which is in agreement with the experiment. The theory also suggests that the area of actual interpenetration of polymer interfaces depends largely on the contact pressure, whereas the depth of penetration appears to depend to a similar degree on both contact pressure and contact time.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 571-573 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 607-614 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A number of empirical equations are presented that are good approximations to computed probability density functions of the one, two and three-dimentional radii of gyration of linear random-flight chains. Equations are given that are in good agreement with the distributions over the range of the radii of most physical interest. Alternative equations are presented that give especially good fit for small values of the one and two-di-mensional radii.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 647-656 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In order to investigate the role of solid morphology on molecular relaxation in crystaline polymers, the effect of melting on the α relaxation in poly(hexamethylene sebacamide) (nylon 610) was measured dielectrically. It was found that the α loss peak was continuous into the melt with respect to location in the frequency-temperature domain and with respect to the shape of the peak. However, the strength of the process, as measured by the difference in the relaxed and unrelaxed dielectric constants, was discontinuous on melting, the process being much stronger in the melt. These observations are consistent with a two-phase model of discrete crystalline and amorphous regions. The relaxation takes place in the amorphous regions, and melting creates more of this material but does not greatly after its nature. The correlation of the amount of amorphous material as measured by dielectric relaxation with that infrared from density measurements is discussed for nylon610, polyoxymethylene, and poly(ethylene oxide).
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 715-720 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The elastic behavior of different types of rubbery polymers (natural rubber, polybutadiene, silicone, and polyisoprene) networks at various degrees of vulcanization and swelling was examined in extension and compression. The data are represented by the Mooney-Rivlin equation. In compression, although C2 is zero, C1 decreases strongly with increasing swelling to a limiting value which, in some cases, may be correlated with the value of C1 found in extension and hence related to the theoretical modulus for highly swollen networks. A possible explanation is presented in terms of supramolecular order in the amorphous materials.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 755-760 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology , Physics
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 767-768 
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    Keywords: Physics ; Polymer and Materials Science
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 823-833 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The melting behavior of isotactic polystyrene, crystallized from the melt and from dilute solutions in trans-decalin, has been studied by differential scanning calorimetry and solubility measurements. The melting curves show 1, 2, or 3 melting endotherms. At large supercooling, crystallization from the melt produces a small melting endotherm just above the crystallization temperature Tc. This peak originates from secondary crystallization of melt trapped within the spherulites. The next melting endotherm is related to the normal primary crystallization process. Its peak temperature increases linearly with Tc, yielding an extrapolated value for the equilibrium melting temperature Tc° of 242 ± 1°C as found before. By self-seeding, crystallization from the melt could be performed at much higher temperature to obtain melting temperatures as high as 243°C, giving rise to doubt about the value of Tc° found by extrapolation. For normal values of Tc and heating rate, an extra endotherm appears on the melting curve. Its peak temperature is the same for both melt-crystallized and solution-crystallized samples, and independent of Tc, but rises with decreasing heating rate. From the effects of heating rate and partial scanning on the ratio of peak areas and of previous heat treatment on dissolution temperature, it is concluded that this peak arises from the second one by continuous melting and recrystallization during the scan.
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  • 158
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 857-861 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It was shown previously that in sedimented mats of solution-grown nylon crystals the 001 wide-angle reflection due to the unit-cell period along the chain and the low-angle reflection due to the lamellar periodicity are both along the same azimuth (meridian) in the x-ray diffraction pattern.1 Presently in photographs which contain both the wide-angle and low-angle regions a series of new meridional reflections have been observed between the low-angle and 001 reflections and between 001 and 002 reflections. This finding implies that, with the large chemical repeat distances in question, diffraction effects at low and wide angles cannot be considered in isolation as is usual in most polymer crystal studies. In particular, the new reflections promise to provide a direct diffraction approach to the structure of the chain-folded lamellae.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 877-886 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Several important aspects of the flow in polymer melts through capillaries remain unexplored. This paper examines experimentally one such effect associated with the radial shear-stress gradient in capillaries. During capillary melt flow of a polymer with a wide molecular weight distribution, migration of the large molecules away from the region of highest shear stress, i.e., at the capillary wall, has been predicted but only modestly investigated. This effect has the potential to produce a molecular weight spectrum over the cross section of extruded polymer. Studies of distribution in shear were conducted on a well-characterized wide-distribution polystyrene (M̄w = 234,000). An Instron Rheometer equipped with a long capillary (length/diameter ratio of 66.7) was used to perform the extrusion at temperatures of 160-250°C. A solvent coring procedure was used to dissolve away concentric layers of polymer from the extrudate for molecular weight analyses. The method has been shown to cut clean sections without selective extraction. Values of M̄w, M̄n and M̄w/M̄n were calculated from complete molecular weight distribution data obtained by calibrated gel permeation chromatography. For a wide range of shear rates and temperatures, no evidence for molecular fractionation was observed. Shear degradation of this polymer was found to be small. However, at high shear rates at 250°C, evidence indicating extensive shear-induced thermal degradation was found. No evidence for oxidative degradation at the extrudate surface was found at either low or high shear rates at this temperature.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 909-918 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A modified BET apparatus has been developed to measure the surface area of polymer samples in the range 0.2-3.0 m2. The sample holder is designed to permit easy entry for bulky samples, such as polymer shavings, which cannot be loaded through a capillary or exposed to the high temperature required to seal glass. Other apparatus modifications, which allow the accurate measurement of surface area, include the addition of a dibutyl phthalate differential manometer in conjunction with a pressure reservoir. Corrections for the dead volume, nonideality of nitrogen, and the thermal gradient in the sample holder are developed. Calibrations of the equipment with inorganic samples of known areas from 1.81 to 11.8 m2 gave highly accurate values of 1.74 to 11.6 m2. Results on high-density polyethylene shavings showed precision in determinations and very close agreement in the value of 49.7 for C in the BET equation with the published value, 47.7.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 957-959 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 975-981 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Samples of cis-polybutadiene were cross-linked in the presence of decalin at values of φr (the volume fraction of rubber) ranging from 0.25 to 0.50. After the diluent had been removed, a study was made of the force-extension and thermoelastic behavior of the networks. Within experimental error, the ratio of the Mooney-Rivlin constants 2C2/2C1 was found to be zero for networks prepared at low φr (0.25 and 0.30) but started to increase towards the conventional value at higher φr. The quantity fe/f was found to be independent of the ratio 2C2/2C1 and of the extension ratio α; the average value of fe/f was found to be 0.11.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1013-1022 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Nylon fibers of various draw ratios have been used as the adsorbents in the adsorption of low molecular weight acids and of polyacrylic acids from solution. Polymer adsorption is lower than on a precipitated nylon and decreases with fiber orientation; however, propionic acid and glutaric acids do not show this dependence on nylon structure. The structural alterations consequent on fiber drawing also reduce swelling in hydroxylated liquids. The greater accessibility of the precipitated nylon is shown by vapor sorption and extends to nonhydroxylated vapors; however, the differences in behavior between polyamide powder and fiber cannot be fully attributed to the former possessing a porous structure, in the sense normally employed in surface chemistry.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1023-1028 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The adsorption behavior on silica of some polystrenes of moderate molecular weight distribution, both singly and in mixtures, has been examined. The adsorption isotherms indicate that, in both a good solvent (trichloroethylene) and under theta conditions, the species of higher molecular weight is preferentially adsorbed at or near full surface coverage, but that the smaller adsorbate has an improved opportunity for adsorption at low surface coverage. The use of tritiated adsorbates substantiate the isotherm data in cyclohexane solution.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1047-1059 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Shear stress P21 and normal stress P11 -P22 functions of moderately concentrated aqueous solutions of sodium poly (acrylate) were measured under steady shear flow at various shear rates \documentclass{article}\pagestyle{empty}\begin{document}$\dot \gamma$\end{document} with a Weissenberg rheogoniometer. The compliance function Js = (P11 - P22)/2P212 is found to vary with shear rate. The double logarithmic plot of Js versus \documentclass{article}\pagestyle{empty}\begin{document}$\dot \gamma$\end{document} can be superposed with respect to molecular weight at constant concentrations of added neutral salt and polymer. These reduced plots differ markedly as the concentration of added salt is varied but converge to a single line at high shear rates.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1085-1095 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In order to study the crazing behavior in rubber-toughened glassy polymers, polystyrene samples containing two rubber balls of the same diameter with varying separations have been prepared. They were subjected to simple tension, and their crazing behavior was observed. When the two balls are close together, the craze-initiation stress is considerably lower than that of single-ball samples. With increase in the distance between the two balls the craze-initiation stress increases at first almost linearly and levels off when l/d reaches about 1.45, where l and d are the center-to-center distance and the diameter of the balls, respectively. When l is sufficiently small, the crazes are seen to develop extensively at the inner surfaces of the balls and finally bridge with each other. The crazes bridged between the balls expand largely in the plane perpendicular to the applied load.
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  • 167
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    Notes: Two linear polyethylene fractions (Mη, 11,260 and 100,000) and mixtures of these fractions have been isothermally crystallized from the melt under pressures up to 3000 atm. Characterization of individually crystallized fractions with transmission electron microscopy indicates that pressure can be used to produce a crystallite whose thickness is a measure of the chain length within it. Although the high molecular weight fraction yields spherulites containing individually varying lamellae thicknesses, the maximum thickness of each lamella is a measure of the chain length within it. Both electron micrographs and differential thermal analysis results show that crystallization of homogeneous mixtures of the high and low molecular weight fractions under high pressure results in a distinct fractionation and segregation according to molecular weight.
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    Notes: A method is described and a computer program outlined whereby gel-permeation chromatographic analysis of fractions from gradient-elution fractionation of branched polyethylenes provides a complete molecular weight evaluation of each fraction and the parent resin. The procedure involves the use of the universal calibration concept of Benoit et al. in a way that eliminates the ambiguities present in attempts to apply it directly to whole polymers. The resultant molecular weight data for fractions, when related to their solution viscosity and low-shear melt viscosity and to their infrared analysis, provides a total structural evaluation of a branched polyethylene resin, including molecular weight molecular weight distribution and the distribution of both long-and short-chain branching. The potential of this method for providing a comprehensive structural evaluation of branched polyethylene is illustrated by examples of its application in the analysis of some commercial resins.
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2255-2258 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 23-42 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Statistical radii of gyration, second virial coefficients, and intrinsic viscosities of sharp fractions (M̄w/M̄n ≈ 1.1) of polyisobutylene (PIB) covering a wide range of molecular weight (1.6 × 105 to 4.7 × 106) were determined in isoamyl isovalerate (IAIV) at a number of temperatures ranging from 20 to 60°C, in n-heptane at 25°C, and in cyclohexane at 25°C by light-scattering and viscosity measurements. It was found that IAIV at 22.1°C is a theta solvent for PIB. Analysis of the data by the methods described in preceding papers of this series indicated that, except for minor differences, the conclusions derived from similar studies with polychloroprene, polystyrene, and poly-p-methylstyrene hold equally for solutions of the typical linear polymer investigated here. In particular, no decisive evidence for the drainage effect was found.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 89-99 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The rate of dissociation of a nonionic detergent, octylphenyl polyoxyethylene ether, was studied by a temperature-jump technique. A relaxation process which is concentration-dependent was observed. A linear relation between the reciprocal relaxation time and the detergent concentration above the critical micelle concentration was obtained, from which the rate constant of dissociation kn,n-1 of one molecule of detergent from the micelle has been determined. Values of kn,n-1 equal to 0.4 ± 0.05 and 73 ± 5 sec-1 at 24.8°C were obtained for detergents with 16 and 30 ethylene oxide units per molecule of surfactant, respectively, showing and increase of the rate constant of dissociation with the length of the hydrophilic-head chain.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 133-150 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Data on tensile strength and elongation at break for a series of Viton A-HV vulcanizates are discussed. The data were obtained at various extension rates at temperatures from -5 to 230°C (25 ≲ T  -  Tg ≲ 260°C) on seven vulcanizates having crosslink densities ve (estimated from C1 in the Mooney-Rivlin equation) from 0.46 × 10-5 to 24.4 × 10-5 mole/cm3. At an extension rate of 1 min-1, an increase in ve affects the tensile strength σb (based on the undeformed cross-sectional area) and the true tensile strength σbσb (based on the cross-sectional area of a deformed specimen) as follows: σb is essentially constant at a low temperature; it passes through a decided maximum at intermediate temperatures; and it increases to a plateau at elevated temperatures. In contrast, λbσb decreases markedly at all temperatures, an exception being the most lightly crosslinked vulcanizate(s). Application of time - temperature superposition to the ultimate-property data gave log aT; its temperature dependence is that typical of nonpolar rubbery polymers. Data on the vulcanizates were compared in corresponding temperature states by plotting log 273σb/T, log 273λbσb/T, and (λb  -  1)/(λb  -  1)max against logtb/(tb)max, where tb is the temperature-reduced time to break and (tb)max is the value at which the ultimate extension ratio λb attains its maximum, (λb)max. Except for the most lightly crosslink vulcanizate, the comparison shows that 273λbσb/T and (λb  -  1)/(λb  -  1)max are substantially independent of (or only weakly dependent on) crosslink density, that 273λb/T increases with ve, and that 273λb/T ∝ ve0.6 and λb ∝ ve-0.4 at a large value of tb/(tb)max.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 159-170 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The decay in birefringence of glassy polycarbonate held at constant extension has been studied at 23°C, in the time-scale range 10-103 sec, up to about 6% strain. The results show that, under these conditions, the birefringence can be validly expressed as a linear hereditary integral of the strain history up to a relatively high strain level which is about 3.4% for an experimental time-scale of 100 sec. Comparison with previously obtained data on the stress relaxation behavior of the same polymer shows that, other factors remaining constant, mechanical relaxation is linear only up to about 1.1% strain. The earlier onset of mechanical nonlinearity is discussed and it is suggested that the mechanical relaxation spectrum is richer than the optical spectrum in relatively long relaxation times, corresponding to relatively slow molecular motions. It is further suggested that these slow molecular motions are accelerated first as the polymer is extended beyond the limit of linear viscoelastic behavior. The observed nonidentity between strain limits for linear mechanical and linear optical behavior is discussed in the light of current practices in photomechanical stress analysis.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1145-1152 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1167-1170 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology , Physics
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1175-1177 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1153-1165 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The anisotropy of the α and β relaxations in oriented poly(ethylene terephthalate) has been studied by dynamic mechanical and dielectric relaxation measurements. The α relaxation shows considerable mechanical anisotropy but gives rise to an isotropic dielectric process. The β relaxation, on the other hand, shows pronounced dielectric anisotropy but very little mechanical anisotropy. The implication of these results with regard to possible interpretations of the relaxations are discussed.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1171-1174 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology , Physics
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1179-1182 
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    Keywords: Physics ; Polymer and Materials Science
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1183-1191 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology , Physics
    Notes: In an attempt to facilitate a better understanding of the role of noncrystallizable components on the crystallization kinetics, spherulitic growth rates as well as the morphology and melting behavior of isotactic polystyrene in blends with various molecular weight atactic polystyrenes (900 to 1,800,000) over a wide range of concentrations have been studied. The growth rates are uniformly depressed with increasing amounts of atactic diluent. In addition, they are dependent on the molecular weight of the added polystyrene, generally decreasing in the molecular weight ranges between 4800 and 19,800 and between 51,000 and 1,800,000. However, between these two ranges, anomalous growth rates showing a sudden increase are observed, which may be explained by an increase in the entrapment of the noncrystallizable diluent. An explanation based on morphological observations, which showed an increase in coarseness of the spherulites with increasing molecular weight of the added atactic polystyrene, is offered.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1193-1206 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The small-angle light scattering in Hv and Vv modes is calculated for elliptical disks with the use of an elliptical coordinate system. The method is general for all degrees of ellipticity, from a circular disk to rodlike extensions, and permits the definition of any desired dipole orientations. The solution is obtained by computer-assisted numeric integration. Two models are considered, an “elliptical” one an “affine deformation” one differing in the orientation of scattering dipoles. The calculated patterns show a significant dependence of the distribution of the scattered intensity on the size and the elliptical axial ratio in both models, permitting the determination of both the size and the degree of ellipticity of the disk from its patterns. In addition, the differences between the calculated results for the two models are sufficiently large to permit the selection of the experimentally appropriate model, at least within the range of moderate degree of ellipticity.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1221-1236 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Crystallite sizes have been obtained from the breadth of equatorial x-ray reflections from polypropylene samples subjected to a draw ratio of 6 at 21°C and then annealed at 155°C, 140°C, and 120°C, respectively. For all samples it was found that the ratio of the dimension of the crystallite perpendicular to the {110} planes to that perpendicular to the (040) plane is a constant. The ratio of the lateral crystallite size to the meridional long period was also found to be constant, independent of annealing temperature. In contrast, the thickness of the crystallites in the direction parallel to the draw direction, as calculated from the meridonal long period and density data, was not proportional to the lateral crystallite size.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1237-1254 
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    Topics: Chemistry and Pharmacology , Physics
    Notes: Wide-angle x-ray scattering (WAXS) patterns of two polypropylene samples, a quenched sample drawn at 21°C and an annealed sample drawn at 100°C, were investigated in a range of values of draw ratio λ very closely spaced through the neck region. In both cases, a range of small λ where deformation occurred by spherulite deformation was followed by one of higher λ where microfibrils were formed. The contribution to the WAXS pattern of microfibrils could be clearly distinguished from that of deformed spherulites because of the better orientation parallel to the draw direction of the former as compared to the latter. Additionally, for a drawing temperature of 21°C, microfibrils crystallize in the “smectic” phase as compared to the monoclinic phase for the initial sample and deformed spherulites. At this temperature, plastic deformation proceeds through the spherulite deformation mechanism up to λ = 1.4 accompanied by an increase in chain orientation with increasing λ. For λ 〉 1.4 plastic deformation appears to occur exclusively through microfibril formation. For drawing at 100°C, spherulite deformation is accompanied by very little change in chain orientation up to λ = 2, where microfibril formation begins. For λ 〉 2 (Td = 100°C) plastic deformation is accompanied by both microfibril formation and some spherulite deformation as reflected by changes in both orientation and crystallite size. At this temperature the lateral crystallite size in the microfibrils is related to the long period according to the “equilibrium crystallite shape” previously found for annealed polypropylene.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1255-1272 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The influence of annealing processes on the thermal behavior of organic glasses in the glass-transition interval has been investigated and analyzed quantitatively. In detailed annealing studies of atactic polystyrene and Aroclor 5460, the absorption of thermal energy superposed on the increase in the specific heat at the glass transition, observed with suitably chosen heating rates, was followed by the differential thermal method. It is concluded that the absorption of thermal energy observed under these conditions parallels the extent of molecular relaxation that has taken place during the annealing period. It is not necessary to postulate a first-order process to account for the energy absorption. Moreover, such a postulate leads to severe conceptual difficulties regarding the development of crystallinity in crystallizable materials. The areas and the shapes of the endotherms are considered in terms of the original physical properties of the quenched glasses and the anticipated equilibrium properties. Relationships between the extent of energy absorption and time-dependent processes such as volume relaxation are discussed.
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1285-1296 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: As part of a study of chemical and physical changes accompanying the formation of carbons by the pyrolysis of polymers, conventional electron microscopy, electron diffraction, and scanning electron microscopy techniques have been used to examine structural and morphological features of polyacrylonitrile (PAN) crystals, powder, and fibers, and of Saran and poly(vinylidene chloride) (PVDC) powder. Changes accompanying the heating of these polymers in air and in nitrogen have been investigated. PAN crystals grown from propylene carbonate were similar to those obtained by Klement and Geil. When heated in air at 220°C they retained their morphology, and electron diffraction gave the same reflections as PAN. On further heating to 400°C in nitrogen the morphology was retained, but the diffraction was lost. Crystals treated in nitrogen alone at 200°C showed morphology similar to that of the polymer. PAN powders and fibers retained discernable external features of their morphology on heating to 800°C. These results are discussed with reference to changes which take place when poly(vinylidene chloride) and Saran are heated in the range 150-180°C, which results in the loss of one hydrogen chloride per monomer unit, and are subsequently carbonized at 800°C. The development of pore structure and the adsorptive properties of Saran carbons are also discussed.
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  • 186
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1207-1219 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dilatometric, calorimetric, and dissolution studies have been made of two crystalline modifications of trans-1,4-polyisoprene in order to determine their equilibrium melting temperatures. This parameter is of fundamental importance in the formal treatment of polymorphism in crystalline polymers. A consistent set of thermodynamic parameters has been derived for both crystalline modifications. The equilibrium melting temperature of the polymorph, which was previously observed to melt from carefully crystallized bulk material at 64°C, was calculated to be at least 82.4°C. The other form, which melts from the bulk at 74°C, has an equilibrium melting temperature of 79.5 ± 0.5°C. The trans-1,4-polyisoprene, crystallized by stirring n-butyl acetate solutions at 49°C, was found by x-ray diffraction to be in the first form and melts at 81.2 ± 0.5°C when very slow heating rates are applied. This melting temperature is very close to the independently derived equilibrium melting temperature and lends support to the possibility that extended chain crystals are present in these solution crystallized crystals. Using the newly found melting temperatures of the two crystalline modifications it can be derived from the free energies of fusion that the first crystalline form is more stable at temperatures above approximately 66°C, whereas the other form is more stable below this temperature.
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  • 187
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1273-1283 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The two endotherms found during DSC analysis of annealed or drawn poly(ethylene terephthalate), PET, are discussed in greater. detail. Earlier workers proposed that the endotherms were the result of separate morphologies, i.e., extended-chain and folded-chain crystals, but more recently Roberts and others have presented data on the effect of DSC heating rate on annealed PET endotherm areas which indicate that the higher temperature endotherm is the result of recrystallization in the DSC. The present work explains the reasons for recrystallization, and presents data showing that samples cooled at various rates from the melt also exhibit recrystallization in the DSC, in much the same manner as samples annealed for different lengths of time. Further, by prolonged annealing before analysis, part of the recrystallization exotherm can be observed in the DSC scan. Drawn nylon 66 also exhibits recrystallization in the DSC, in a manner similar to annealed or slowly crystallized PET. The amount of material that recrystallizes is determined by the time and supercooling available between first melting and the ultimate recrystallization temperature, i.e., a temperature at which there is too little time and temperature driving force for further recrystallization to occur. Infrared absorption data show an increase in “regular” fold content during prolonged annealing of PET, while dynamic mechanical data show a marked decrease in a dispersion that is likely associated with the looser fold crystal morphologies. Annealed PET does superheat in the DSC, leaving unanswered the question as to whether any partially extended material is present along with the regular-fold material. For cold-drawn PET, the infrared data indicate disappearance of regular folds and the dynamic mechanical data indicate disappearance of the looser folds. Cold-drawn PET also superheats. These data indicate a likelihood of at least partially extended morphologies in cold-drawn PET; these observations do not apply to PET drawn at high temperatures or to polyethylene.
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  • 188
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1297-1304 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The glass transition temperature of systems based on epoxy resin and a number of diamines has been determined by using a torsion pendulum. An equation relating composition and crosslink density with the glass transition temperature has been established which gives reasonable predictions of the glass transition temperatures for systems based on aliphatic or aromatic amines and methylated amines and for systems containing a monofunctional epoxy diluent. The equation may be used to predict Tg for systems with non-stoichiometric quantities of curing agent and blends of amines. Deviation of the predicted and observed values for Tg is interpreted in terms of differences between definitions of Tg used by other workers and, also the occurrence of competing side reactions during polymerization which lead to additional crosslinks.
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  • 189
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1305-1319 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The relaxation behavior of nylon 6 from 4.2 to 300°K was investigated as a function of orientation, anisotropy and moisture content by using an inverted free-oscillating torsion pendulum. Three new relaxations, δ at 53°K, ∊ below 4.2°K, and ζ at 20°K, were discovered. The characteristics of these new relaxations strongly depend on the orientation anisotropy, and concentration of adsorbed water in the specimens. The results suggest that the mechanism of the γ process is associated with the motions of both the polar and methylene units. The mechanism of the β relaxation is postulated to originate with motions of both non-hydrogen-bonded polar groups and polymer - water complex units. The behavior of the α peak is consistent with the hypothesis that it originates with the rupture of interchain hydrogen bonding due to the motions of long-chain segments in the amorphous regions. Finally, the data strongly support the proposition that two types of water, tightly bound and loosely bound, exist in nylon 6.
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  • 190
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1337-1349 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Two types of emulsion-grade polytetrafluoroethylene particles have been studied. We refer to these as ribbons and rods. The ribbons consist of very thin ribbons or lamellae folded upon themselves a number of times. In typical emulsion-grade material prepared at Allied Chemical, the unraveled ribbon measures about 3.25 μ in length, 0.25 μ in width, and 60Å in thickness. The folded ribbons, which form the particles, are about 0.5 μ long and 0.25 μ wide. Electron diffraction shows that the ribbons are single crystals with the chain axis parallel to the long axis of the ribbons thus forming extended chain crystals. This extended-chain packing is consistent with the observed cleavage or fibrillation of the ribbons and with the molecular weight. The rods are formed in low-yield polymerizations. Electron diffraction also shows that the rods are single crystals with the chain axis parallel to the long axis of the rods. Striations parallel to the long axis are believed to result from stacking of parallel segments. Considerable bending of the long axis of rods is observed.
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  • 191
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1321-1336 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Transient photocurrents in poly(vinyl chloride) films are shown to be due to photo-injection of electrons from metallic cathodes. Most of the injected electrons are promptly trapped, but some drift across the sample to the anode under the influence of an external electric field. The mobility of these electrons, determined by transient photoconductivity techniques, is 4.7 ± 0.5 × 10-4 cm2/V-sec at 27°C, and rises to 3.4 ± 0.5 × 10-3 cm2/V-sec at 43°C, the measuring cell having been evacuated to a pressure of 10-6 torr at both temperatures. Diffusion of helium into the samples appears to decrease the electron, mobility. It is suggested that electron transport is correctly described by using an energy-band model for intramolecular motion and an activated hopping model for intermolecular transfer. Oscillations observed in the transient photocurrents in the frequency range 103-105 Hz are attributed to electron avalanche formation at the anode, with photosuccessors.
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  • 192
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1361-1367 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: From a model of delocalized triplet energy in an aromatic vinyl polymer, the relative efficiency of triplet-energy transfer to either an added or copolymerized quenching molecule is determined. It is found that copolymerization can increase the photoprotective efficiency only if the quenching rate is determined by the final energy transfer step. A study of the quenching of polystyrene phosphorescence by added or copolymerized naphthalene indicates that there is no enhancement of quenching efficiency by copolymerization.
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  • 193
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1351-1359 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The elongational viscosity of dilute polymer solutions must always be measured under nonsteady-state conditions. To predict the time dependence of this viscosity for a polymer solution in which a constant stretching rate is maintained, a simple model is considered in which the polymer molecules are represented by elastic dumbbells. The non-Hookean elastic force in the dumbbell is determined by the conformational entropy of the chain. Use is made of Peterlin's approximation which replaces the elastic force by a function of the root-mean-square end-to-end distance. Application to the transient state is straightforward; it can be extended to include the effect of “internal” chain viscosity by means of approximations that are similar to Peterlin's.
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  • 194
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1397-1400 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 195
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The conformational energies for (1→4)-linked α-D- and β-D-galactans have been computed by considering nonbonded, torsional, and electrostatic interactions. The electrostatic interactions are estimated by assigning the charges to various atoms in the molecule by the method of Del Re. The characteristic ratios CN = 〈r2〉0/Nlv2 are computed for α-D- and β-D-galactans as a function of the degree of polymerization N and the angle τ at the bridge oxygen atom. These values of characteristic ratios obtained for α-D-galactan are very much higher than for β-D-galactan, indicating that the former assumes a highly extended conformation compared to the latter. The values of characteristic ratios of both these polysaccharides show a decrease with increase in τ similar to that observed for other (1→4)-linked polysaccharides. The calculated values of C∞ of (1→4)-linked polysaccharides show no correlation with the number of allowed conformations but are affected both by the orientation of the interunit glycosidic bonds and the hindered potential associated with chain units. It has also been shown that the magnitude of the steric factor σ may not be used as an index of flexibility for polysaccharides which differ in type of linkage.
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  • 196
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1401-1405 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 197
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An investigation was made of the dynamic mechanical behavior in the rubberlike region of poly(n-butyl methacrylate) (PBuMA) and poly(n-butyl acrylate) (PBuA) networks lightly crosslinked with ethylene dimethacrylate to concentrations from 10-6 to 10-4 mole/cm3. The measurements were carried out by use of an apparatus for low-frequency forced vibrations working in the frequency range 2.5 × 10-4 to 1 Hz. With parameters c1 and c2 of the Williams-Landel-Ferry equation, obtained from data in the main transition region, the data did not reduce in the rubberlike region for the poly(butyl methacrylate) networks; the spread of the deviations decreases with increasing concentration of the crosslinking agent. Superposition could be achieved in all cases when a shift factor was used on the vertical axis. At sufficiently low reduced frequencies and at high temperatures the storage compliance decreases in both series of polymers with increasing concentration of the crosslinking agent as expected. At higher reduced frequencies and at higher temperatures of measurement, however, anomalous behavior was observed with uncrosslinked samples having a lower compliance than those crosslinked to a very low degree. This finding was explained as due to very long relaxation times of the untrapped entanglements present in the noncrosslinked polymer, which are absent in the same polymer crosslinked already to very low degrees. The retardation spectra of both PBuMA and PBuA exhibited secondary relaxation mechanisms which were shifted by four logarithmic decades toward higher retardation times in comparison with the primary retardation maximum.
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  • 198
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1407-1414 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The methods of Hermans and Weidinger and of Wakelin et al. (the correlation and integral methods) were used to determine the degree of crystallinity in poly(ethylene terephthalate) (PET) fibers. A standarization of cutting of the amorphous background scattering in PET fibers, indispensable for the method of Hermans and Weidinger, is put forward. On using a partial standardization of the intensity diffracted and scattered in the fiber, namely, on taking into account the x-ray density of the specimen, variability in the intensity due to differences in absorption in the specimen at different angles 2θ and variability in the specimen mass reflecting x-rays in the function of the diffraction angle, good agreement of the PET fiber crystallinity values is observed.
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  • 199
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1415-1445 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A reaction rate model of fracture in polymer fibers is described. This model assumes that bond rupture is governed by absolute reaction rate theory with a stress-aided activation energy. It is demonstrated that the key in obtaining good agreement between the model and experiment lies in taking proper account of the variation of stress on the tie-chain molecules. The more taut chains rupture first, and the load is redistributed among the remaining unruptured tie chains. The effect of varying the temperature both in the model and in experiments on fracture in fibers is explored. Good agreement between predictions of the model and experiment is possible only with an undeterstanding of the distribution in stress on the tie chains. The distribution in stress on the chains was experimentally determined by monitoring the kinetics of bond rupture with electron paramagnetic resonance (EPR) spectroscopy. Temperature is found to have two effects on macroscopic strength. (1) The thermal energy aids the atomic stress in breaking the atomic bonds; as a consequence the rate of bond rupture of a family of bonds under a given molecular stress is increased. In this respect temperature might be viewed as decreasing the “strength” of a bond. (2) Temperature also serves to “loosen” the molecular structure and in this way modify the distribution in stress on the tie chains. To explain bond rupture and macroscopic fracture behavior quantitatively, account must be taken of both effects.
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  • 200
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    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1447-1459 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In order to obtain information about a possible helix-coil transition of isotactic polystyrene (i-PS) at 80°C in toluene, as has been reported in other solvents, solution properties were examined at temperatures between 10 and 110°C. Use was made of viscometry, high-resolution nuclear magnetic resonance, infrared spectroscopy, calorimetry, and light scattering. No distinct transition was found at 80°C but rather a second-order transition between 62 and 65°C. A similar transition occurred in toluene solutions of atactic polystyrene. The transition may be attributed to a sudden change in the mobility of the phenyl side-group of the polymer. From this study it is concluded that i-PS has a helical conformation in toluene, the mean helix length decreasing smoothly with increasing temperature.
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