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  • 1970-1974  (2,547)
  • 1930-1934
  • 1890-1899
  • Physics  (2,547)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1163-1175 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Highly polished surfaces of nylon 6, nylon 66, polychlorotrifluoroethylene and polypropylene were etched by aromatic and chlorinated hydrocarbons at temperatures between 25 and 75°C to reveal surface morphology. Comparison with micrographs obtained with microtomed sections shows the absence of etching artifacts which are known to accompany the use of oxidizing etching agents.
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  • 2
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1207-1209 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1371-1381 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Small-angle polarized light scattering from a deformed three-dimensional spherulite is formulated on the basis of the deformation model proposed in Part II of this series. The intensity distribution of scattered light is discussed chiefly for the cross-polarization condition, the so-called Hv polarization, as a function of elongation of the spherulite. In the undeformed state, the scattered intensity distribution forms the typical fourleaf clover pattern, and the intensity decreases with increasing fraction of crystals oriented randomly (type R crystals) within the crystal lamellae of the spherulites. In a system composed of type R crystals and folded-chain crystals (type B crystals) within the lamellae, the four-leaf pattern moves to the horizontal zone near the equator with increasing elongation of the spherulite, and, simultaneously, extends to some extent to the vertical zone near the meridional direction as a parameter measuring the ease of lamellar untwisting increases. In a system composed, in addition to type R and type B crystals, of crystals transformed from type B to type Ca and type Cr due to tilting and unfolding of polymer chains, respectively, within the crystal lamellae an eight-leaf pattern appears, even at small elongation up to about 30%. Each lobe of the eight-leaf pattern undergoes a characteristic change with increasing elongation. In both systems, the scattered intensity increases with sharpening of orientation distribution of crystals within the crystal lamellae.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1441-1456 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The theory of Franklin et al. is employed for the calculation of the maximum form birefringence of a polymer having lamellar morphology. The results confirm the experimental conclusion that for low-density polyethylene, the form birefringence approaches 3% of the total birefringence. The theory also predicts the parabolic dependence of the form birefringence on the refractive index of the amorphous phase. It may be applied to estimate the dynamic form birefringence and leads to a value of the dynamic strain-optical coefficient which is of the order of 2-15% of the total.
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  • 5
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1477-1483 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of drawing on the glass-transition temperature of amorphous poly(ethylene terephthalate) has been studied. The Tg decreases to a minimum at a draw ratio of 1.5, then increases to a maximum at a draw ratio of about 2.0, and again decreases with increasing draw ratio. The relationship between the change of structure and Tg is discussed in terms of the configurational entropy and the rate of molecular motion in local-mode relaxation. On the basis of configurational entropy, the decrease of Tg at the beginning of drawing depends on the increase of configurational entropy, while at draw ratios above 2.0 it depends on the increase of entropy associated with intermolecular interaction. From the point of view of molecular motion, it is concluded that the change of Tg is determined by local oscillations in the amorphous region.
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  • 6
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1537-1546 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Free electrophoresis, differential spectral UV analysis, and the determination of the coefficients of selective sorption were used to investigate, in aqueous solutions of halides, the behavior of two polycations, poly[1(2-hydroxyethyl)pyridinium methacrylate] and poly[1(2-hydroxyethyl)trimethylammonium methacrylate]: i.e., one species with and the other without a pyridine ring in the side chain. Electrophoretic data were used to estimate the length of the electrophoretic segment and the approximate charge of the polyion in solutions of the individual salts. A comparison of the data showed that the interaction is not due to the presence of the pyridine ring in the side chain and that the order of activity of the halide anions is the same for both types of polymers.
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  • 7
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1565-1574 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: When isotactic polystyrene (i-PS) is crystallized from the melt or from the glassy state at rather large supercooling an additional melting peak appears on the curve during scanning in a differential calorimeter. The overall rate of crystallization deduced from the total peak areas as a function of crystallization time did not fit the Avrami equation well. When we omit the area of the additional melting peak in the kinetic analysis a much better fit is obtained. We also observed that no lamellar thickening occurs during isothermal crystallization. In view of the low degree of crystallinity of i-PS these results lead to the idea that a secondary crystallization process takes place within the amorphous parts of the spherulites resulting in this additional melting peak on the DSC curve. The large supercooling needed and the increase in peak area with increasing molecular weight make us suppose that intercrystalline links are probably responsible for the additional melting peak of bulk-crystallized i-PS. Electron microscopic studies of surface replicas of i-PS support this view.
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  • 8
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1639-1648 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The theory of the preceding paper is compared with previously unpublished experimental results on the viscoelastic properties of two polystyrene fractions of molecular weight 1.9 × 106 and 1.2 × 106 in nitropropane, which is very nearly a theta solvent, and in toluene, a good solvent. At the concentrations used, around 1%, the theory predicts extensive departures from non-draining toward free-draining behavior; these effects are observed. The theory similarly fits experimental data of Johnson on a sample of polystyrene of molecular weight 860,000 in decalin and dioctyl phthalate in the same concentration range.
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  • 9
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1849-1856 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Main-chain scission was the predominant effect when dilute solutions of three linear polystyrenes in 1-methylnaphthalene and polybenzyl oligomer received up to 2000 megaroentgen of 1.5-MeV electrons. Values of energy per scission were independent of dose and of the same magnitude as literature values in dioxane and benzene solutions when compared at the same dose rate. In all cases as irradiation progressed, Mw/Mn approached a value of 2 and Mz/Mw approached a value of 1.5 characteristic of a random distribution. Starting from one initial distribution, random numbers were used to simulate random chain scission. A 500 MR (megaroentgen) distribution calculated in this manner matched the experimental distribution after a 500 MR irradiation.
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  • 10
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1865-1874 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The relationship between the critical point and the precipitation threshold is examined in the Flory - Huggins approximation with concentration-independent interaction parameter χ. Approximate explicit expressions for the difference between the critical point and the threshold can be derived by series expansion of threshold conditions. In the first-order approximation, the concentration difference depends only on the chainlength averages xw, xz, and xz+1, in the second-order approximation it depends on xw, xz, xz+1, and xz+2, etc. For polymers of low polydispersity, the second-order approximation gives a good estimate of the concentration difference; for instance, for polymers with exponential distribution and xw/xn 〈 1.25, the error is lower than ca. 1%. The approximation is not suitable for polymers with xz+1 ≫ xz (including polymers whose cloud-point curve exhibits a triple point). Irrespective of the polydispersity of the polymer, the threshold as well as the whole cloud-point curve depend only on the weight-average and higher averages, xw, xz, xz+1, …, xz+k, where k → ∞; they are, however, independent of the number average xn.
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  • 11
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    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1925-1937 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The glass-transition region of crosslinked polymers prepared from poly(1,2-propylene phthalate fumarate) and styrene was studied using a torsion pendulum. The glass-transition temperature and the modulus in the rubbery region of these polymers were analyzed in terms of the crosslink density. The styrene concentration at which the maximum crosslink density occurs, as estimated from the viscoelastic data, is found to be in agreement with estimates made by other workers using chemical methods.
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  • 12
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 13
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2209-2251 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Stress crazing is studied in three forms of crystalline, isotactic polypropylene (PP): (1) smectic/nonspherulitic, (2) monoclinic/nonspherulitic, and (3) monoclinic/spherulitic PP. Optical and scanning electron microscopy as well as stress - strain measurements are used to characterize crazing behavior in these three forms as a function of temperature (-210 to 60°C) and of the gaseous environment (vacuum, He, N2, Ar, O2, and CO2). Forms 1 and 2 are found to craze much like an amorphous, glassy polymer in the temperature range between -210 and -20°C, irrespective of environment. The plastic crazing strain is large close to the glass-transition range (ca. -20°C) of amorphous PP and in the neighborhood of the condensation temperature of the environmental gas. Near condensation, the gas acts as a crazing agent inasmuch as the stress necessary to promote crazing is lower in its presence than in vacuum. A gas is the more efficient as a crazing agent, the greater is its thermodynamic activity.Spherulitic PP (form 3) crazes in an entirely different manner from an amorphous, glassy polymer, showing that the presence of spherulites influences crazing behavior much more profoundly than the mere presence of a smectic or monoclinic crystal lattice. Below room temperature, crazes are generally restricted in length to a single spherulite, emanating from the center and going along radii perpendicular, within about 15°, to the direction of stress. They never go along spherulite boundaries. Gases near their condensation temperature act as crazing agents much as in nonspherulitic PP. Above room temperature the crazes are no longer related to the spherulite structure, being extremely long and perfectly perpendicular to the stress direction. Apparently the crystals are softened enough by thermally activated segmental motion to permit easy propagation of the craze. The morphology of the fracture surfaces and its dependence on temperature and environment is described and discussed. Concerning the action of gases as crazing agents it is argued that the gas is strongly absorbed at the craze tip, where stress concentration increases both the equilibrium gas solubility and the diffusion constant. Hence, a plasticized zone is formed having a decreased yield stress for plastic flow. This is considered to be the main mechanism by which the gas acts as a crazing agent. In addition, reduction of the surface energy of the polymer by the adsorbed gas eases the hole formation involved in crazing.
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  • 14
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2267-2280 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effects of swelling and annealing treatments on viscoelastic behavior were studied in melt-crystallized and solution-crystallized samples of isotactic polypropylene (iso-PP) over the temperature range -150 to 150°C. The log E″ versus T curves exhibited α, β, and γ peaks in order of decreasing temperature. The β peak of the melt-crystallized sample shifted to higher temperatures after annealing, but was not affected by swelling. The α peak of melt-crystallized polymer was affected by swelling treatments. It increased in height and shifted to lower temperatures almost linearly with the volume fraction of absorbed solvent. The magnitude of the shift was independent of the solvent species - toluene, p-xylene, tetralin, carbon tetrachloride - however, it depended significantly on the temperature at which the sample had been heat treated. For solution-crystallized polymer, no peaks in log E″ were observed in the temperature range of the β peak of melt-crystallized material, but the α peak appeared larger and broader, and at higher temperature than the corresponding peak in the melt-crystallized polymer. After swelling or annealing, the low-temperature component of the α peak of the solution-crystallized sample decreased in height and at the same time a new loss peak appeared at -55 and 0°C, respectively, is swollen and annealed samples. In particular, in the case of annealing treatments, the high-temperature component of the α peak shifted to still higher temperatures. From these results on the solution-crystallized sample it can be deduced that the segmental motions in the amorphous phase are very strongly constrained by surrounding crystalline phases as compared with those in the amorphous phase of the melt-crystallized sample, and the constraints imposed on the segmental motions are released to a great extent by both treatments. Finally, swelling effects on the γ peak were examined. The γ peak of the melt-crystallized sample decreased in height after swelling. On the other hand, the γ peak of the solution-crystallized sample separated into two peaks, which might be attributed to the mechanical relaxations in the crystalline and amorphous phases.
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  • 15
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2347-2360 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Viscosity and normal stress behavior were measured for poly(methyl methacrylate) samples of various average molecular weights in diethyl phthalate solution at 30 and 60°C. All samples conformed approximately to the most probable distriution (M̄w/M̄n = 2). Concentrations ranged from 0.113 to 0.38 g/ml, and M̄w from 53,800 to 1,620,000. Despite considerable evidence in the literature of unusual linear viscoelastic behavior for this polymer, its nonlinear properties appear to be rather conventional. The viscosity-shear rate master curve was similar to that found earlier for concentrated solutions of polystyrene and poly(vinyl acetate) of comparable molecular-weight distribution. The viscosity time constant τo parallels τR, the characteristic time of the Rouse model, although the residual dependence of τo/τR on concentration and molecular weight appears to be slightly different from that for polystyrene and poly(vinyl acetate). Similar conclusions apply to the recoverable compliance Je,o estimated from the normal stress behavior of each solution, and its relationship to the Rouse model compliance JR.
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  • 16
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2361-2374 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Mixtures of butyl rubber with polyisobutylene (molecular weights 0.055 and 2.3 × 106) up to 50% by weight were crosslinked by sulfur, leaving the polyisobutylene molecules free to reptate in the butyl rubber network. Linear viscoelastic properties were measured in shear creep for periods up to 5 × 105 sec at 25°C and oscillating shear deformations from 0.1 to 3 Hz, at temperatures from 2 to 63°C. Comparison with the properties of a butyl rubber crosslinked without polyisobutylene showed contributions to creep and mechanical loss attributable to the reptating species. Comparison with the properties of polyisobutylene (higher molecular weight) showed that the relaxation times associated with the reptating species in the upper part of the terminal zone are the same for different polyisobutylene contents (25% and 50%) and for 100% polyisobutylene in which no permanent network is present; their contributions to modulus appear to be proportional to the volume fraction of polyisobutylene to a power of about 2/3. The time required in stress relaxation for the portion of the modulus attributable to the reptating species to decay to half its plateau value is, based on the two molecular weights employed, proportional to the polyisobutylene molecular weight to the third power. The magnitude of the associated mechanical loss and its location on the frequency scale can thus be controlled independently.
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  • 17
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2413-2422 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dynamic viscosity of dilute aqueous solution of poly(methacrylic acid) (PMA) was measured over the frequency range 2-500 kHz for various degrees of ionization. The relaxation spectrum calculated from the viscosity exhibits a conformational relaxation spectrum in the short-time region and a rotational one in the long-time region. The former is fitted by the Zimm theory over the entire range of ionization, including the transition from a compact structure to an open one. The conformational relaxation time begins to increase at the midpoint of the transition region, but the rotational relaxation time increases very markedly in the initial stage of the transition.The present and previously reported experimental findings are interpreted in terms of the assumption that the compact structure is stabilized by short-range methyl-methyl bonding as well as “long-range” methyl-methyl bonding (bonding between methyl groups spatially close but remotely connected along the chain contour). In the initial stage of the transition, the latter primarily break up, resulting in expansion of overall chain dimensions, and subsequently the former are destroyed, resulting in the change in local chain conformation.
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  • 18
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2465-2472 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The photoelectret properties of poly(N-vinyl carbazole) sandwiched between a conducting glass electrode and an aluminum electrode have been studied. Photoelectret polarization was carried out by simultaneous application of an electric field and ultraviolet illumination. The polarization exhibits a linear dependence on the polarizing voltage, polarization time, and illumination intensity, with saturation effects for large values of these parameters. The depolarization current decay is quite fast, which indicates the absence of deep-trap levels. The ratio of photoelectret charge to the dark polarization charge is found to be 100, which determines the image contrast if the polymer film is used in persistent internal polarization (PIP) electrophotography.
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  • 19
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 223-238 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The structure of poly(N-methyl laurolactam) has been studied in the solid state and in solution. In oriented, annealed monofilaments, the chain exhibits a distorted extended planar zigzag conformation. Upon orientation, an increase in crystallinity and a slight shift of the large d spacing in the diffraction pattern to a higher value is observed. In the crystalline regions of the polymer, the amide groups are proposed to have the anti conformation, whereas the amorphous regions may consist of both the syn and anti forms. Differential scanning calorimetry and thermal mechanical analysis showed multiple melting endotherms which probably result from partial melting and reorganization of small, imperfect crystallites. In solution, nuclear magnetic resonance spectroscopy showed the presence of a conformational equilibrium of the syn and anti amide groups in the polymer chains. The effect of thermal and mechanical treatments on certain infrared group frequencies of the amide moieties was studied and correlated with other pertinent analytical data.
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  • 20
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2397-2397 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 21
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2423-2436 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polyethylene was prepared by γ-ray-induced polymerization in the temperature range 0-180°C. The morphology and the physical properties of the polymer as polymerized were studied by electron microscopy, differential scanning calorimetry, and gel permeation chromatography. Aggregates of small lamellar crystals with irregularly growing faces were produced below 55°C. Aggregates of large spherical particles were formed above 60°C together with hemispherical particles which adhered to the substrate. A few lamellar crystals of triangular or amoeba-like shapes were also found above 55°C. The polymers formed below 55°C showed a sharp single endothermic DSC peak and a bimodal molecular-weight distribution, while the sample above 60°C had a double endotherm and a unimodal molecular-weight distribution. These facts suggest that the mechanism of crystallization during polymerization below 55°C is different from that above 60°C. The melting point, however, decreased continuously with increasing polymerization temperature and was much lower than that of extended-chain crystals. The results show that the polyethylene, as polymerized, is composed of folded-chain crystals irrespective of the reaction temperature.
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  • 22
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2473-2491 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Densified glasses, formed from the liquid state by cooling at 5°C/hr under elevated pressures of up to 517 MN/m2, were studied by thermal analysis and dilatometry at ambient pressure. The materials studied were polystyrene, poly(methyl methacrylate), phenolphthalein, sucrose, and a 1 : 1 mixture by weight of potassium and calcium nitrate. Enthalpies of the densified glasses were found to be up to 2-6 J/g greater than the enthalpies of the glasses formed at atmospheric pressure. The major enthalpy and volume relaxation on heating the densified glasses was found to be not correlated The upper temperature limit of the glass-transition region remained constant for all glasses cooled at various pressures, while the lower temperature limit of the polymeric glasses decreased up to 55°C with increasing pressure. The interpretation of the data suggests that an additional, significant volume relaxation occurred on depressurization at room temperature for all glasses analyzed.
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  • 23
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2535-2549 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The marked effects of chemical structure on the morphology of single crystals in linear aliphatic polyesters have been investigated. Drawn fibers and solution-grown crystals of poly(ethylene sebacate), poly(hexamethylene sebacate), and poly(decamethylene 1,16-hexadecanedicarboxylate) have been studied by small-angle and wide-angle x-ray diffraction. Electron microscopy, and broadline NMR provided supplementary information.The crystal disorder due to irregularity in the cross section of the molecule due to ester groups along the chain direction increases with increase of the methylene sequence length in the chemical repeat unit. On the basis of the x-ray data and electron microscopy, it is proposed that the nature of the fold surface of single crystals of a given polymer, especially a choice of (001) or (hkl) fold surface (flat lamellae or hollow pyramidal crystals), is determined by energetic competition effects between fold geometry and unit cell symmetry. A smooth increase of the long period with increasing crystallization and annealing temperature seems to be general behavior even when a pronounced stepwise increase might be anticipated.
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  • 24
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2579-2581 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 25
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 441-443 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 26
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 735-761 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A theory is developed by use of the correlation function approach for calculating both the Hv and Vv intensity of scattered light for a concentrated assembly of spherulities. The scattering becomes a function of the radial and tangential polarizabilities of the spherulite αr and αt, the polarizability αm of the medium, surrounding the spherulites, and the volume fraction φs of spherulites. The “effective polarizability of the surroundings” αs, which appeared in previous theories, becomes function of these variables. The theory can explain, for example, why the Vv scattered intensity passes through a maximum during the course of crystallization.
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  • 27
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 763-784 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A lattice theory of orientational disorder in two-dimensional spherulites is developed in which the orientation direction of the optic axis in lattice cells is allowed statistically to deviate from its mean value in a manner correlated with the orientation in neighboring cells. The Hv light scattering patterns arising from such disordered spherulites deviate from the patterns for perfect spherulites in that there is excess intensity at both small and large scattering angles and the intensity at the maximum is lower. A comparison of the calculated scattering angular dependence with that which is experimentally measured permits assignment of values of correlation parameters. A consequence of this disorder is that the spherulite birefringence is reduced below that calculated on the basis of perfect crystalline orientation in agreement with experiment.
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  • 28
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 813-814 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 29
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 819-821 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
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  • 30
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 849-869 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of molecular weight distribution on mechanical properties of concentrated polymer solutions was studied by measuring creep compliance and complex modulus for solutions of binary blends of narrow distribution polystyrenes in chlorinated biphenyl. Two-step plateaus in the rubbery plateau region, as reported for undiluted polymer blends, were observed for concentrated solutions provided the molecular weights of component polymers differed greatly. The nth order blending law (n = 1, 2, 3) of Bogue et al. was simplified in form to compare with experimental results. As far as the present version of simplification was concerned, the cubic blending law was better than the quadratic one in describing viscoelastic properties of polymer blends. The cubic blending law reproduced closely the magnitudes of viscoelastic functions such as loss modulus and relaxation modulus but it was not able to predict the two-step plateaus, even when the ratio of molecular weights of components was as large as 10. It also provided a good approximation to reported results on the steady-state compliance Jebo for undiluted binary polymer blends and present results for solution blends. Since the cubic blending law in the simplified version was consistent with previous results on concentration dependence of the steady-state compliance for concentrated solutions of narrow distribution polymers, it gave a unified expression for the steady-state compliance of binary polymer blends and concentrated solutions of narrow distribution polymers.
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  • 31
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 925-939 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The chemical and physical crosslink densities of irradiated polybutadiene were determined using a precise and consistent method. This method included the use of a statistical theory of crosslinking modified to include chain reactions and the use of Langley's theory for calculating the number of trapped chain entanglements. The number of crosslinks formed per unit radiation dose, G(X), was measured for a series of polybutadienes containing various isomeric forms of unsaturation. The physical crosslink density and the molecular weight between entanglements were determined from measurements of the compression modulus of swollen samples.
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  • 32
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 977-989 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Injection-molded specimens of nylon 6 were examined by x-ray diffraction as a function of depth in three characteristic directions. A skin and a core were always found to be present which differed in the degree of crystalline perfection and crystal modification. While the core of pure nylon 6 was found to be not oriented, the core of specimens containing nucleating agents was found to contain a typical texture of the monoclinic modification of nylon 6 in which the distribution probability of the a* and c* axes resembles ellipsoids with three unequal axes. A model explaining this texture as due to degenerated (deformed) spherulites is proposed. With a transcrystalline nylon 6 specimen the direction of the fastest growth in the unit cell (which forms the radius of spherulites) is found to be close to the a axis.
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  • 33
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1189-1193 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics of the disappearance of propagating butadiene radicals produced in the grafting of butadiene to poly(vinyl chloride) was followed by electron spin resonance measurements. The radical species observed in the temperature range 213-298°K is the conjugated allylic radical: \documentclass{article}\pagestyle{empty}\begin{document}$$ \hbox{---} {\rm CH}_{2}\hbox{---}\rm{CH}\hbox{=\hskip-1pt=}{\rm CH}\hbox{---}{\rm CH}_2 \rightleftharpoons\hbox{---}{\rm CH}_2\hbox{---}{\rm CH}\hbox{---}{\rm CH}\hbox{=\hskip-1pt=}{\rm CH}_2 $$\end{document} The reaction conditions were adjusted to provide a highly viscous medium in which the propagation reaction took place. Under these conditions the radicals were stabilized and a precise ESR spectrum was obtained. Arrhenius plots of the second-order decay rate constants yield an activation energy of 5 kcal/mole. This suggests that the bimolecular termination reaction is controlled by the segmental motion of the grafted side chains.
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  • 34
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1215-1220 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 35
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1235-1238 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 36
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1727-1731 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 5 Ill.
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  • 37
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1743-1751 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: For the model of an elastic dumbbell, i.e., two beads connected by a Hookean spring, the Langevin equations for the beads are formulated. It is taken into account that the friction force contains terms resulting from the inertia of the liquid. The contribution of the dumbbell to the viscosity is calculated from the rate of energy dissipation. When the inertia of the liquid is neglected, the viscosity contribution reduces to Kramers' result and is independent of the mass of the beads. When the inertia terms are added, the result is nearly independent of this mass, but shows a dependence on the density of the liquid. In liquids of low viscosity, the extra term resulting from the inertia may be as large as 25% of the total viscosity contribution.
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  • 38
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1805-1823 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The scattering from an assembly of anisotropic rods having correlated orientation is calculated in terms of a correlation function expressing the probability of parallelism of orientation of their optic axes as a function of their separation. The scattering is dependent upon the product of a form factor for the scattering from an individual rod and an interference factor dependent upon this correlation function.
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  • 39
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1857-1864 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Four polymers, viz. polystyrene, polycarbonate, poly(methyl methacrylate), and poly-(vinyl chloride), were cooled from the melt to room temperature under hydrostatic pressures of 30 and 1000 atm. Cooling under high pressure increased the density by 0.4-0.6%, and the effect of this has been examined for the torsional creep properties, the dynamic properties at 1 Hz, the Charpy impact strength, the thermal expansivity, and the torsional yield stress. It turned out that, in general, densification affects the thermomechanical properties only slightly.
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  • 40
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1825-1848 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Processes that impart strength and toughness are discussed along with reinforcement by colloidal plastics to indicate that high strength, except under restricted test conditions, necessitates a dispersed phase. Thereafter the dependence of the nominal and true tensile strengths on the type, size, and concentration of polar segments in polyurethane elastomers is considered. Data are first examined on formulations devoid of plastic domains and then on those containing domain-forming segments that result from the reaction of toluene-2,4-diisocyanate (TDI) with either toluene-2,4-diamine or 4,4′-methylene-bis-(2-chloroaniline) and from the reaction of 4,4′-diphenyl methane diisocyanate (MDI) with 1,4-butanediol (BD). Segments from TDI and either diamine give plastic domains that are especially effective for augmenting strength over an extended temperature range. Segments from MDI and BD are comparatively ineffective, although the formulation studied exhibits high strength at and below room temperature owing to strain-induced crystallization. From data on various segmented and triblock elastomers, general conclusions are drawn regarding the dependence of strength on the characteristics of the domains and the matrix. For some six segmented and triblock elastomers, it is found that the true tensile strength is essentially independent of the weight fraction of domains provided it exceeds 0.20 or thereabouts.
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  • 41
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2177-2187 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The rheological behavior of dilute solutions of flexible macromolecules is studied by means of a freely jointed multiple bead-rod model. The solution of the equations describing the mechanics of the system is obtained by means of a numerical procedure, which applies to arbitrary flow conditions. The case of the transient stress in uniaxial elongational flow is developed in some detail. A comparison with bead-spring models shows both quantitative and qualitative differences which are briefly discussed.
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  • 42
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2253-2266 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Cryoscopic measurements have been carried out on solutions in sulfuric acid of a heterocyclic polymer, its monomers, and certain of its oligomers. The polymer, BBB, is prepared by the polycondensation of 1,4,5,8-naphthalenetetracarboxylic acid (NTC) with 3,3′-diaminobenzidine (DAB). The results show that the polymer, its oligomers and one of its monomers, DAB, are all extensively protonated in sulfuric acid, whereas its other monomer is not. The degree of protonation appears to be greater for the polymer than for its low molecular weight oligomers.
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  • 43
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2291-2308 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: To describe the characteristic crystalline structure of polyolefins, Pennings first proposed a model consisting of a combination of an extended chain crystal (a “shish”) and folded chain crystals (“kebabs”). In Pennings' model the “shish” forms first during a crystallization process under stress and then later the “kebabs” overgrow this “shish” structure epitaxially. Because we had some doubts about such a mechanism, we undertook a series of experimental studies on linear polyethylene, particularly in regard to the crystallization process from a solution under shear. Our conclusion is that the crystals grow first by a screw dislocation mechanism, like whiskers, and then later these are deformed by the shear stress to form the shish kebab structures.
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  • 44
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2319-2330 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new, more realistic optical model of a dilute polymer solution is used to calculate the intrinsic birefringence. A general formula is derived valid for an arbitrary equilibrium distribution function of particles in the system. Besides the contributions due to the polymer and solvent, the resulting relation for intrinsic birefringence also contains terms reflecting the effect of orientation of solvent surrounding the polymer chain and the contribution of optical interactions between polymer segments and molecules of solvent. A detailed discussion of the optical interactions in an isotropic solvent reveals that the problem may be transformed in the first approximation into that of interactions between excess dipoles; however, any separation of the macroform and microform effects has no theoretical justification. It is shown that the microform effect depends on a detailed optical model of the statistical segment, and this effect is calculated for two simple models. The expression suggested by Tsvetkov cannot be applied to a segment consisting of anisotropic monomers.
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  • 45
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2375-2391 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A systematic study of solution-grown polyethylene crystals in the electron microscope using dark-field imaging in several diffracted beams has warranted a detailed analysis of the moiré patterns recorded. Direct proof for the existence of tilt moiré patterns has been obtained for the first time, while parallel and tilt patterns have been positively distinguished. Consideration of the formation conditions and properties of moiré patterns in dark field has been extended to include interference between an electron beam diffracted in both participating crystals with one diffracted in only one of them. Examples of moiré patterns depending thus on double diffraction have been identified.
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  • 46
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2577-2578 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
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  • 47
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2551-2565 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Crystallization and melting behavior of linear polyethylene under high pressures up to 6000 kg/cm2 has been investigated with a high-pressure dilatometer. Crystallization was carried out at a cooling rate of 1°C/min from the melt at each pressure. The samples were characterized by differential scanning calorimetry, density, and electron microscopy. Folded-chain crystals are formed in the low-pressure region below 2000 kg/cm2. Crystallization in the intermediate-pressure region between 2000 and 3500 kg/cm2 gives a mixture of folded-chain and extended-chain crystals. The extendedchain crystals are the more stable and predominate at increasing pressure. At high pressures above 4700 kg/cm2, two stages of crystallization and of melting can be observed. The phenomenon suggests that the two kinds of extended-chain crystals with different thermal stability, i.e., the ordinary extended-chain crystals and “highly extended-chain” crystals form through individual crystallization processes from the melt at high pressure.
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  • 48
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 115-130 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Effects of neutralization on butadiene-methacrylic acid copolymers have been studied. In Hycar CTB with 2% acid groups, small-angle x-ray scattering gives evidence of some cation clustering and leads to a value of the mean radius of 5.6 Å for the clusters and a value of the distance between them of 70 Å. When the concentration of salt is increased there is no appreciable change in the distance between clusters or in their size, but their number increases. The structure of clusters has been studied by electron paramagnetic resonance in copolymers neutralized with copper salts. The appearance of a line as in the monohydrated acetate salt permits one to define the structure of clusters consisting of two Cu2+ and four RCOO- ions with two H2O or RCOOH molecules. When the temperature is increased, the signal corresponding to Cu2+-Cu2+ pairs disappears. In high molecular weight butadiene methacrylic acid copolymers with 9% acid groups, we have found the ion pair clusters gathered into larger clusters. In dynamic mechanical properties, a relaxation peak appears at 340°K. We interpret this as due to breaking and possible re-forming of dipolar associations.
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  • 49
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 217-220 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
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  • 50
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 445-454 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The fundamental vibrational frequencies of an isolated chain of cis-1,4-polybutadiene have been calculated. Infrared and polarized Raman data are used in the force constant refinement routine. The assignments of the vibrational frequencies are discussed in terms of the potential energy distribution.
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  • 51
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 485-500 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The equilibrium and kinetics of gas sorption by a silicone rubber filled with highly adsorptive molecular sieves was studied. Sorption in this system is by two mechanisms: gas is simply dissolved in the polymer matrix according to Henry's law, while it is adsorbed by the dispersed sieve phase in accordance with a Langmuir's isotherm. The latter effectively immobilizes the gas molecules preventing their further diffusion. All equilibrium parameters were determined experimentally. Immobilization greatly affects sorption kinetics and renders conventional analyses invalid. A theory to account for this process was adapted from a previous analysis by Vieth and Sladek which assumes that the kinetics of adsorption is very fast compared to diffusion. For this situation the kinetics always assume a Fickean form. The experimental data agreed very well with the predictions of this theory in a comparison where all parameters were defined by independent experiments. It was found that a single effective diffusion coefficient describes sorption kinetics, steady-state permeation, and time-lag results once the effects of immobilization are properly accounted for.
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  • 52
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 501-513 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Heterogeneous network polymers composed of rigid polypeptide chains and flexible polyether chains were synthesized. That is, poly(L-glutamic acid) (PLGA) was crosslinked with poly(oxyethylene glycol) (PEG) at various carboxy/hydroxyl mole ratios K. The solubility tests and hydrolysis of heterogeneous network polymers suggest that the crosslinking reaction proceeds by esterification. The dynamic mechanical properties of these polymers(100 Hz, -100-200°C) are greatly influenced by the presence of a trace of water and the weight per cent of PLGA. In addition, some of these polymers show only one maximum in the temperature dispersion of dynamic loss modulus E″ and tan δ, although their shape is rather broad. The x-ray photographs of these polymers show an amorphous halo or weak Debye-Sherrer rings. These findings suggest that these polymers are not simple adducts; neverthless PLGA and/or PEG domains exist.
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  • 53
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 555-562 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The rules formulated by Koningsveld for the determination of the critical concentration are shown to be in accord with the Flory-Huggins theory. Sometimes, however, they may not refer to stable conditions, and their application in such cases will result in misleading conclusions.
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  • 54
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 563-578 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Four samples containing 40, 60, 80, and 97 wt-% of poly(vinyl chloride), the rest being plasticizer and stabilizer, were tested by using the Weissenberg Rheogoniometer in the steady-shearing mode at temperatures between 155 and 235°C and rates of shear \documentclass{article}\pagestyle{empty}\begin{document}$ \dot \gamma = 0.01 - 400 $\end{document} sec-1. The viscosity η versus \documentclass{article}\pagestyle{empty}\begin{document}$ \dot \gamma $\end{document} follows Graessley's theoretical dependence for infinitely entangled system. The primary normal-stress difference coefficient ψ versus \documentclass{article}\pagestyle{empty}\begin{document}$ \dot \gamma $\end{document} is well described by the same theoretical function, used with the square of its argument. The temperature dependence of η0 and ψ0 shows discontinuities at T = Tb. The numerical values of Tb can be calculated from the theory of the melting point depression due to diluent. The activation energy of viscous flow Eη below Tb is 5-9 times as large as above this temperature. The activation energy of normal stress is found to be Eψ ≈ 5Eη. The characteristic relaxation times τo, ψp, calculated from superposition of η versus \documentclass{article}\pagestyle{empty}\begin{document}$ \dot \gamma $\end{document} and ψ versus \documentclass{article}\pagestyle{empty}\begin{document}$ \dot \gamma $\end{document} data, respectively, onto Graessley's master curves, and τN, computed from zero shear parameters η0 and ψ0, differ in their sensitivity to the melting of microcrystalline regions. It is postulated that in the systems investigated, aggregates with long lifetimes are being formed, increasing the effective molecular weight and introducing changes in the effective polydispersity.
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  • 55
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 633-633 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 56
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 635-643 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Semicrystalline polymers generally exhibit moduli well below their theoretical limit due to chain folding and to lack of crystal alignment. Modulus increases attainable through standard drawing procedures are limited by sample fracture before large draw ratios are reached. Using an Instron capillary rheometer which allowed a draw ratio of 〉 300, transparent polyethylene strands of unusually high c-axis orientation have been produced by a combination of pressure and shear. The virtually perfect crystalline orientation and evidence for extended chains confirm that a significant improvement in modulus can be realized by this technique. The dynamic tensile storage modulus was measured by Vibron over the temperature range -160°C to +120°C. Room-temperature moduli were 7 × 1011 dyne/cm2, higher than any reported values for drawn polyethylene. Values also remained above 1011 dyne/cm2 even at 120°C. The moduli and morphological data have been related by a model consisting of an extended-chain component in paralled with a conventional drawn morphology. Experimental and calculated moduli are compared and related to available theory.
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  • 57
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 665-683 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polystyrene radically polymerized in atmosphere of air is composed of bisegment (C-A) or trisegment (C-A-C) block copolymers consisting of styrene segment (A) and styrene peroxide segment (C). Dielectric measurements of a system of copolymers of styrene and oxygen were obtained above the glass temperature. Three primary relaxations, a, b, and c, in order of descending temperature, were found corresponding to three microphases: styrene phase (phase a), styrene peroxide phase (phase c), and an intermediate phase (phase b) which contains a low concentration of peroxide bonds. An alternating copolymer of styrene and oxygen exhibits the relaxation c alone. With heat treatment above the glass temperature, relaxation c and subsequently relaxation b vanish with thermal degradation of peroxide bonds. The sum of relaxation strengths is linearly related to the content of peroxide bonds which was evaluated by the elementary analysis and DTA. Below the glass temperature, the temperature dependence of dielectric loss of carefully purified polystyrene without peroxide bonds shows very weak peaks which correspond to γ (200°K at 10 kHz) and δ (50°K at 10 kHz) peaks, respectively, in the activation plot. When low molecular degradation products of peroxide bonds are occluded or impurities such as benzaldehyde are added into the specimen, the height of the γ peak is appreciably enhanced, indicating that the reorientation of small polar molecules in polystyrene accompanies the vibration of the phenyl group about the C—C6H5 bond which gives rise to the γ relaxation.
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  • 58
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 703-712 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An amorphous polypropylene sample was examined by using 13C NMR at 25.2 MHz and all ten possible methyl resonances from monomer pentads were observed. Assignments were made through a consideration of an additivity relationship among the methyl resonances. Confirmation for the assignments was obtained through observed conformity of the methyl resonance intensity distribution with second-order Markov statistics. The relative intensity distribution of the methyl resonances can be used to characterize the structure of polypropylenes with confidence, since experimentally it is shown that an equal nuclear Overhauser effect exists for each of the methyl resonances.
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  • 59
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1015-1022 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A diffraction contrast study with the aid of an image intensifier was undertaken to obtain direct evidence for the existence of a mosaic block structure in polyethylene single crystals grown by self seeding under isothermal conditions. Dark-field microscopy indicates that the crystals do not contain a mosaic block structure. High-resolution electron diffraction confirms that the crystal is coherent (i.e., mosaic block-free) over regions of several thousands of Angstroms. It is concluded that a mosaic structure on the scale of ∼300 Å does not exist in polyethylene single crystals grown under carefully controlled conditions from dilute solutions. Possible reasons for previous results that indicate the presence of a ∼300 Å mosaic block structure are discussed.
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  • 60
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1035-1052 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dynamic viscosity of aqueous solutions of poly(acrylic acid) at a polymer concentration of ca. 0.15 g/100 ml has been measured at frequencies from 2 to 500 kHz as a function of degree of polymerization P, degree of neutralization α, and salt (NaCl) concentration Cs. Relaxation spectra have been obtained from the dynamic viscosity. The spectra in the short relaxation time region can be approximated by the Zimm theory for the conformational relaxation of nonionic polymers. The maximum relaxation time τ1 of the Zimm spectra is proportional to P2 and depends rather moderately on α and Cs. Increased deviation is found, however, in the long relaxation time region, in particular for high values of P and α and low values of Cs. The major part of the deviation is interpreted in terms of rotational relaxation of a molecule as a whole. The rotational relaxation time τR is proportional to P3 and increases with increasing α and decreasing Cs. The remaining part of the excess spectra located between τ1 and τR is ascribed to the deviation of the conformational relaxation from the Zimm theory arising from ionization of the polymer.
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  • 61
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1117-1126 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Single crystals of cellulose triacetate II (CTA II) free of crystallization solvent can be grown from dilute solution in mixtures of dibenzyl ether and n-tetradecane. Good results are obtained by using a polymer fraction with a degree of polymerization of 60 and a mixture of 70% n-tetradecane and 30% dibenzyl ether at 245°C. The lamellar crystals produced are lozenge-shaped with the longer diagonal parallel to the a axis of the lattice and with {110} as the growth faces. Twin growth occurs frequently with {110} as a twinning plane and less frequently with {210}.
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  • 62
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1109-1115 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Thermoluminescence of polycarbonate irradiated by electron beams was observed in order to investigate the trapping of electrons and the luminescence mechanism. The thermoluminescence glow curve is composed of three components. The peaks appear at -150°C (α peak), -120°C (β peak), and -30°C (γ peak). The α peak is attributed to recombination of cations with electrons released from trapping sites formed by carbonate groups. The β peak is attributed to small amounts of impurities. The γ peak is perhaps due to untrapping of electrons from the phenoxy anion. The luminescence intensity of the α peak is linearly dependent on the absorbed dose, and that of the β peak is approximately proportional to the cube of the dose. The appearance of these peaks is presumably closely related to local molecular motions.
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  • 63
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1239-1243 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 64
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1255-1258 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 65
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1319-1325 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The birefringence of an object is usually obtained from its retardation. For an object of variable refractive index and optic axis orientation, a matrix procedure should be used for relating the retardation to the birefringence. There are many cases in the literature where this correct procedure has not been used. The correct procedure is illustrated for the case of a polymer spherulite.
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  • 66
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1355-1370 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: p-Divinylbenzene has been polymerized by heating at pressures ranging from atmospheric to 2.5 GN/m2, and the moduli (Young's, shear, and bulk), density, and residual unsaturation of the products have been determined. The results show a marked effect of polymerization pressure upon density and upon the degree of conversion of the second double bond. Linear relations are indicated between modulus and either density or an intermolecular force function based on a 6-12 potential field. These results and others on the densification of polystyrene are discussed and it is concluded that the moduli of the poly-p-divinylbenzene samples prepared under these conditions are still at a level largely determined by intermolecular forces.
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  • 67
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1955-1968 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A general method is described to take into account the multiple scattering effect in a small-angle light scattering from thin polymer films. It is seen that multiple scattering tends to make the scattering envelope more diffuse, reducing the intensity in the high intensity regions and increasing it in the low intensity regions. The method is applied here to a spherulitic system, but it is valid for any other system where the principal scattering is in the forward direction.
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  • 68
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1875-1887 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dielectric properties of poly(vinylidene fluoride) have been studied in the frequency range 20 Hz to 1 MHz and between 100 and 220°C, during heating and cooling. The dielectric constant and loss change abruptly at the temperature Tm corresponding to the melting point. At lower frequencies, two types of ionic conductin are observed. One appears below Tm and is attributed to interfacial polarization. The other occurs above Tm and is related to electrode polarization. These results suggest that a crystalline polymer is a heterogeneous medium for ionic transport, while the melt is a homogeneous medium. From these results, the nature of ac ionic conduction in crystalline polymers is discussed. At high frequency, the α relaxation is observed below Tm. It is due to the molecular motion in the crystalline region and disappears at Tm.
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  • 69
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1939-1940 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 70
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1993-2018 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The polymerization and crystallization of diazomethane was analyzed starting with various monomer and catalyst concentrations by following the monomer concentration and analysis of the solid polymethylene produced. Electron microscopy, thermal analysis, x-ray diffraction, and viscometry and density determinations were used to characterize the crystals as produced and after etching with nitric acid. The crystals have a fibrillar and a lamellar component and show no regular chain folding of the molecules. The overall process follows only very approximately the path expected for an ideal living-polymer system capable of reaction in solution and in the solid state. For more detailed correspondence, it was necessary to assume two reaction paths and two crystallization paths.
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  • 71
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2281-2290 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The molecular relaxation behavior of poly(dimethyl siloxane) (PDMS) exposed to various gases pressurized to 207 megapascals (MPa) was investigated by pulsed nuclear magnetic resonance spectroscopy. For a gas of low solubility, such as helium, the gas acts only as a pressurizing medium allowing the effect of pressure on the glass transition to be determined. For gases of high solubility the gas acts not only as a pressurizing medium but also as a plasticizing agent, expanding the polymer lattice and increasing the frequency of molecular motions. The plasticizing effect of argon was found to increase the temperature dependence of the molecular correlation frequency.
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  • 72
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2309-2317 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Crystallization processes occurring during polymer synthesis in a nonsolvent medium are discussed. It is concluded that in the case of heterogeneous polymerization of ethylene the polymer is produced as a supercooled liquid surrounding the catalyst particles. These particles then coalesce until a critical size is reached allowing a high nucleation probability. Thus coalescence coupled with polymerization, leads to crystallization at a relatively uniform particle size. Two less usual polymerization catalyst systems, VCl3 produced by a high-frequency discharge in VCl4 vapor, and the mixture of TiCl4 and Al(CH3)3 vapors (an apparently homogeneous system) are used to illustrate these concepts for polyethylene.
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  • 73
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2331-2345 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics of isothermal crystallization of polyethylene under high pressures ranging from 840 to 5300 kg/cm2 has been studied dilatometrically. The crystallization rate estimated from the half-time of the overall transformation increases markedly with pressure. The Avrami exponent n becomes smaller with increasing pressure. Values of n ≈ 2 for the crystallization at 840 and 1950 kg/cm2, and n ≈ 1 at 5100 and 5300 kg/cm2 were obtained. Differential scanning calorimetry and electron microscopy data are presented. It is concluded that extended-chain crystals grow rapidly, predominantly in one dimension, at high pressure. Relations between log k and Tm/T(ΔT) and Tm2/T(ΔT)2 are nearly linear. Here, k is the crystallization rate constant from an Avrami equation, ΔT = Tm - T, Tm is the melting point, and T is the temperature of crystallization. From the dependence of the slope of the straight line on the crystallization pressure it is concluded that the surface energy of crystal nuclei decreases with increasing pressure.
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  • 74
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2393-2395 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 75
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2455-2463 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A simple mechanical model based on the equilibrium rate theory of Burte and Halsey is presented in order to explain the stress-strain curve of polypivalolactone (PPL) fibers. A semiquantitative application of this model indicates that the PPL alpha-beta transformation implies the cooperative deformation of at least thrity chain units and that the free energy difference between the alpha and beta states is of the order of 2 kcal/mole of monomer.
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  • 76
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The energy level dispersion, along the chain wave vector, of infrared-active methylene rocking modes has been measured as a function of pressure to 40 kbar for a number of polymethylenes. They are crystalline polyethylene and n-paraffins C23H48, C24H50, C28H58, and C29H60. The crystalline factor-group splitting of each chain mode is observed at various pressures, for those polymethylenes which have orthorhombic or monoclinic structures. The effects of crystal structure, intermolecular force field and intramolecular force field on the observed energy levels as well as on the crystalline factor-group splittings are discussed A hydrogen-hydrogen nonbonded repulsion potential has been calculated as a function of interatomic distance rH••H for 2.3 Å 〈 rH••H 〈 3.0 Å from the observed volume dependence of the factor-group splittings of methylene rocking modes. It is shown that the dynamic potential wells along the normal coordinates of the rocking modes are harmonic up to room temperature.
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  • 77
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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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  • 78
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 97-114 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: New data are reported for the permeation of inert gases through polyethylene, polytetrafluoroethylene, and silicone and natural rubbers. Additional data are compiled from the literature. The relative solubilities of these gases are practically insensitive to chemical variations in the homopolymer. Hence variations in structure at the glass transition (Tg) and melting (Tm) temperatures that affect diffusion also unambiguously affect permcation. Consequently an equivalence results between permeation at a given temperature for different polymers and permeation at different temperatures for a given polymer. Although the diffusion coefficient changes continuously with temperature, the Arrhenius parameters Do and Ed apparently change discontinuously at Tg and Tm. Their magnitudes and variations with atomic weight reach maxima at about Tg. These data indicate a dependence of the classical correlation between Do and Ed on polymer properties. A perturbed diameter for the permeant, specific for each polymer, is proposed for correlating the Do and Ed data. This correlation makes the changes observed at Tg and Tm more perceptible.
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  • 79
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 159-173 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Samples of poly(4,4′-isopropylidenediphenylene 1,1,3-trimethyl-3-phenylindan-4′,5- dicarboxylate) were fractionated by the column-elution, temperature-gradient technique. Selected fractions, covering a 10-fold range of molecular weight, were shown to have narrow molecular weight distributions by gel-permeation chromatography (GPC), i.e., M̄w/M̄n = 1.15 ± 0.10. The fractions were further characterized by viscometry, light scattering, and membrane osmometry. Characterization of the small samples (ca. 0.3 g) was facilitated by use of a low-volume light scattering cell. This allows measurements of refractive increment, light scattering, and viscosity to be performed on as little as 50 mg of sample. Molecular weights estimated by the GPC-viscometry technique were in good agreement with the values obtained by light scattering. Estimates of the perturbed coil dimensions (150-200 Å) were in satisfactory agreement with those observed experimentally. The polydispersities of the fractions, determined by osmometry and light scattering, were in fair agreement with GPC data; the latter are considered subject to less experimental uncertainty.
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  • 80
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 213-216 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 81
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 239-254 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The influence of the solvent-nonsolvent gradient and the temperature gradient on the efficiency of the precipitation chromatography is investigated with radically and anionically prepared polystyrene samples. Only a combination of both gradients gives optimal effectiveness of the column. The separating power of the column was determined by using mixtures of well defined samples. From the elution curves of the mixtures the nonuniformity Ufr of fractions can be estimated. For fractions of anionically prepared polystyrenes Ufr is on the average 0.001; this value is of the same order of magnitude as the statistical error. These results show that with this chromatographic method it is possible to determine the narrow molecular weight distributions of anionically prepared polystyrenes (or other polymers) with an accuracy sufficient for kinetic studies.
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  • 82
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 295-301 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The adhesion to glass of rubbers with different relaxation properties but similar surface condition has been compared using the thin film peel test. At higher peeling stresses, the rubber-glass interface fractured at constant velocity and all rubbers gave the same adhesive energy values. However, at lower peel stresses, the lossy rubber appeared to adhere more strongly due to a crack-slowing phenomenon at the rubber-glass interface.
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  • 83
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 335-358 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In order to elucidate the relationship between dielectric behavior and structure in solid polymers, we studied the dielectric relaxation of stereoregular poly(methyl methacrylate) (PMMA) in the glassy state. Assuming that the extremes of molecular structure are attained in the crystal and in solution, the most probable conformation of the main chain in the glassy state is estimated for isotactic and syndiotactic PMMA in terms of conformational analysis, the unperturbed mean-square end-to-end distance in solution, and the NMR second moment in the glassy state. Under the assumption that the molecular structure varies in a limited range near the most probable conformation and that the α-methyl group rotates freely, the energy barrier for the rotation of the side group is calculated. With the calculated energy barrier, the dielectric relaxation due to the side group is interpreted fairly satisfactorily by the barrier theory of Hoffman and Lauritzen, although the width of the relaxation curve is not. The experimental result that the loss peak of syndiotactic PMMA is located at higher temperature than that of isotactic PMMA is interpreted qualitatively in terms of different conformations for the syndiotactic and isotactic chains.
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  • 84
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 359-384 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A Raman band of low frequency, arising from an accordionlike vibration of all-trans \documentclass{article}\pagestyle{empty}\begin{document}$ \rlap{--} ({\rm CH}_2 \rlap{--})_n $\end{document} segments and previously observed in normal paraffins and in polyethylene single crystals, has now also been found in bulk and in cold-drawn polyethylene, both linear and branched. The accordionlike vibration, or longitudinal acoustic mode (LAM), in polyethylene is compared with the LAM in normal paraffins. Whereas the Raman bands corresponding to the third (LAM-3) and higher modes are quite intense in a long-chain paraffin such as n-C94H190, they are so weak in polyethylene as to be unobservable with the apparatus used. This is attributed to the presence of the chain fold in polyethylene. Of the two extreme structural models of the fold here discussed, namely the models of “tight folds” and of “loose loops,” only the latter seems capable of accounting for the weakness of LAM-3 and higher modes in polyethylene. A quantity called “nominal Raman length” is defined as the length of that all-trans n-paraffin that would have the same LAM-1 frequency as the polyethylene sample under consideration. The nominal Raman length is always greater than the average long spacing, deduced from discrete x-ray scattering at small angles after applying a Lorentz correction, and, after allowing for chain tilt, is found equal to the segment length between folds. This can be accounted for by both of the models mentioned. As a test of the theory of surface melting the frequency of the accordion vibration of annealed polyethylene single crystals was measured as a function of temperature up to the melting point; no frequency change with temperature was observable. On the basis of the naive idea that there is complete decoupling of the vibrations in the all-trans chain segment from the disordered (molten) surface layer, one would predict that upon surface melting and the concomitant shortening of the all-trans segment, the LAM-1 frequency should increase. A more careful analysis, taking into account the existence of coupling of the LAM to the surface layer, shows that the outcome of this experiment does not necessarily invalidate the idea of surface melting. Bulk polyethylene samples exposed to 60Co γ-radiation for doses up to 100 Mrad show a slight shift of the Raman band to lower frequencies, whereas no such shift was observed upon absorption of a swelling agent. A search, without success, was made for a longitudinal acoustic mode in polypropylene, poly(vinylidene fluoride), nylon 66, and polyoxymethylene.
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  • 85
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 617-628 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A deviation from Graessley's theory of entanglement viscosity appears at very high shear rates when the flow of polydimethylsiloxanes of various molecular weights and their solutions with various concentrations is measured by the capillary method. In order to explain this deviation, a modified Graessley theory is proposed according to the previously reported suggestion that frictional viscosity appears not to be negligible at high shear rates. A reducing procedure taking a frictional viscosity parameter into account was performed. All of the reduced data are combined to give a master curve in spite of a wide range of molecular weight, concentration, and shear rate (from the lower Newtonian to very highest non-Newtonian flow region). The findings from the reducing procedure completely explain the mechanism of non-Newtonian flow for the bulk polymers with various molecular weights, including those below the critical molecular weight for entanglement, and for polymer solutions at any concentration. The viscosity of the linear polymer system consists of the shear-dependent entanglement term ηent proposed by Graessley and the shear-independent frictional term ηfric. The non-Newtonian behavior depends on the ratio of ηent/ηfric at the shear rate of measurement. The ratio of zero-shear entanglement viscosity ηent,0 to ηfric and the critical shear rate for onset of the non-Newtonian flow may be used as a measure of the non-Newtonian behavior of the system and a measure of capability for its rising, respectively. The Graessley theory is to be included in the present modified theory and is applicable to the case of ηentηfric ≫ 1.
    Additional Material: 5 Ill.
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  • 86
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 633-633 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 87
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 645-654 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The NMR spectra of water adsorbed at various relative humidities on various cellulose ester membranes have been studied. Membranes of cellulose acetate (CA), cellulose triacetate (CTA), and cellulose acetate butyrate (CAB) were investigated. It was found that the resonance peak of a liquid imbibed in or adsorbed on membranes from high relative humidity is very sensitive to the angle between the membrane plane and the direction of the magnetic field, shifting 5-7 ppm to higher fields as the membrane plane is rotated from a perpendicular to a parallel position with respect to the direction of the external magnetic field. This phenomenon was found to be independent of the nature of the polymeric material (namely CA, CTA, or CAB), porosity of the membrane (varying from an “all bulk” dense sheet to an 80% porosity and 0.2 μm average pore size membrane), nature of the magnetic nuclei (H2O or D2O), intensity of the external magnetic field (60 Mcps or 100 Mcps), and nature of the liquid in the membrane (water, methanol, or n-hexane). It is therefore concluded that the dependence of the position of the resonance peak on the position of the membrane plane with respect to the external magnetic field, is a geometrical phenomenon due to the magnetic “bulk susceptibility” of the medium. Quantitative estimations of the magnitude of the diamagnetic susceptibility effect in a cylindrically rolled sheet are given. These estimates agree well with the experimentally observed “splittings.”
    Additional Material: 5 Ill.
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  • 88
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 685-693 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The spin-spin relaxation time T2 and the fraction of short T2 component for composites of natural rubber with carbon black prepared under various conditions have been measured by pulsed NMR. Effect of swelling with a solvent (CCl4), carbon black species (SAF, HAF, SRF) with different surface areas, and different initial carbon black loadings (35, 50, 70 phr) have been determined. Molecular motion in the rubber phase not in the immediate vicinity of the carbon black surface increases rapidly with increasing solvent concentration, yet it is still slightly restricted compared to rubber with solvent alone. On the other hand, molecular motion in the immobilized layer around carbon black and the fraction rubber in that layer are not affected by the solvent. This indicates strong restriction of molecular motion of polymers at the surface. For estimation of the thickness of the immobilized layer, the necessity of using an appropriate measure of surface area accessible to polymer molecules is pointed out. The degree of immobilization in the layer and the thickness of the layer do not vary appreciably with the nature of carbon black or the initial loading of carbon black.
    Additional Material: 3 Ill.
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  • 89
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1081-1088 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The fracture and craze surfaces of four PVC fractions (M̄w = 51000 to 228000) and two bimodal blends were examined with a scanning electron microscope. The fraction with the lowest molecular weight gave brittle fractures when fatigued in nitrogen and ethanol vapor. Walls of crazed ductile matter formed at the surface of higher molecular weight samples. Thickness of this ductile material increased with molecular weight. There appeared to be a balance between craze propagation into the sample and brittle fracture due to dilitational and tensile stresses in the interior regions of the test films.
    Additional Material: 9 Ill.
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  • 90
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1251-1254 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
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  • 91
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1619-1637 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The theories of viscoelasticity of chain-molecule solutions, based on the bead-spring model, have been modified to take into account approximately the effect of interactions among chain molecules. The motion of a given chain molecule has been analyzed in detail while all other chain molecules have been treated as a background of uniformly distributed beads in which the given chain molecule is suspended. The inclusion of intermolecular interactions leads to a hydrodynamic interaction tensor, which after averaging, differs from that of Kirkwood by a concentration-dependent correction term. The modified theory correctly predicts the transition from the non-draining to the free-draining behavior which has been observed in chain-molecule solutions as their concentrations are increased.
    Additional Material: 3 Ill.
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  • 92
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1707-1709 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 93
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1-6 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of poly(vinyl formal) membranes was synthesized by formalization of poly(vinyl alcohol) membranes. Representative pieces were selected for this study. Some cellulose acetate membranes cast from dioxane were used for comparison. The main experimental techniques employed included water absorption measurements and direct osmosis measurements. Aqueous solutions of sodium chloride at various concentrations were used for the studies of permeation through the membranes by direct osmosis.The plot of water permeability coefficient Pw versus volume fraction Vw of water absorbed in a membrane was interpreted in terms of the effect of two different types of absorbed water molecules. The individual diffusion coefficients were evaluated from asymptotic slopes of the curves. Similar analyses applied satisfactorily to data found in the literature.
    Additional Material: 3 Ill.
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  • 94
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 23-34 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: DSC traces and specific heat data for poly(p-diphenyl acrylate) (PPBA) and poly(p-cyclohexylphenyl acrylate) (PPCPA) obtained by radical polymerization are reported. The results indicate the existence of a definite ordered phase and of a reversible firstorder solid-liquid transition in both polymers although x-ray diffraction studies showed that they are not crystalline in the conventional sense. The extent of the ordered phase present in each polymer is calculated, and the problems involved in such determination by thermal measurements are discussed. On the basis of the experimental results reported here in conjunction with the x-ray data, models are proposed for the morphology of these polymers.
    Additional Material: 11 Ill.
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  • 95
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 81-87 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Stress-strain relationships are calculated for three models of the deformation of monocrystalline polytetrafluoroethylene, \documentclass{article}\pagestyle{empty}\begin{document}$ \rlap{--} ({\rm CF}_{\rm 2} \rlap{--} )_n $\end{document}. The physical models comprise either sliding one molecule or one plane of molecules parallel to the molecular chain axis past its stationary neighbors. The potential energy is calculated for each stage of deformation by semiempirical methods by use of 6-exp and dipole-dipole interactions. Application of Eyring's activated complex theory leads to stress-strain relationships. These are compared with results of friction measurements on PTFE.
    Additional Material: 1 Ill.
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  • 96
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 265-287 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The predictions of a model presented previously are tested with data on five styrenebutadiene-styrene copolymers. Differential scanning calorimetry and laser light transmission are the primary tools, spanning 180-630°K, with some evidence supplied also by electron microscopy and mechanical properties. The existence of a first-order phase transition, characterized by a separation temperature Ts, is verified and found to be predictable by the model. Details of morphology, including transitions in microstructure in certain temperature ranges, are also reported and shown to be consistent with the theory.
    Additional Material: 21 Ill.
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  • 97
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 317-333 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The morphological features of random block copolymers of tetramethyl-p-silphenylene (TMPS) and dimethylsiloxane (DMS) have been studied as a function of copolymer composition. Wide-angle and small-angle x-ray diffraction coupled with several electron diffraction and microscopy studies were used to investigate these materials. The results of this work clearly indicate that the amorphous segments do not enter into the crystalline lattice of the crystallizable component which is varied in content from 90% to 30%. Over the entire range of compositions the block copolymers are crystallizable. Spherulites can be grown from the melt, and single crystals and/or spherulites may be obtained from solution. Single crystals can be obtained over the entire range of compositions provided ample time is allowed for crystallization. The crystalline TMPS component exhibits tetragonal symmetry at all compositions. The amorphous phase manifests itself as a diffuse halo in patterns obtained by electron and x-ray diffraction.
    Additional Material: 12 Ill.
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  • 98
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics of isothermal crystallization from the glassy state at low temperatures and the morphology of poly(ethylene terephthalate) (PET) filled with additives are reported. Talc, kaolin, silicon oxide, and titanium oxide have been used as fillers; they act as effective nucleating agents for PET. The overall rate of crystallization depends on the volume concentration, the size distribution, and the nucleating ability of the additives. An electron microscopic study reveals a transcrystalline morphology at the surface of the filler particles. The occurrence of transcrystallinity is attributed to extensive heterogeneous nucleation induced at the filler surface. From the shape of the crystallization isotherms, it can be concluded that the crystallization mechanism depends on the type of filler.
    Additional Material: 9 Ill.
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  • 99
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    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 399-406 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The nonlinear integral equations governing phase transition kinetics with homogeneous nucleation and growth site impingement are developed and solved to the first order for the two-dimensional case. It is shown that the fractional transformed area at time t is given approximately by a(t) = Kt3/(1 + Kt3). The iteration method used to get the solution is applicable to certain other nonlinear differential and integral equations. It is shown that the theory predicts the total number of growth sites formed, and that the nucleation rate and growth constants can be deduced from this and the gross kinetic data. The extension of the method of three-dimensional growth is indicated.
    Additional Material: 1 Tab.
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  • 100
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 417-429 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A study of the effect of excluded volume on the mean-square optical anisotropy 〈γ2〉 and the mean-square end-to-end distance 〈R2〉 has been carried out for polymer chains of up to 2000 bonds. The calculations have been made for models assuming (a) equiprobability of internal rotations and (b) interdependence of short-range intramolecular interactions. All the results indicate that 〈γ2〉 is practically insensitive to the excluded-volume effect. Concomitantly the behavior of 〈R2〉 has been analyzed.
    Additional Material: 5 Ill.
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