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  • Articles: DFG German National Licenses  (980)
  • 1970-1974  (980)
  • 1945-1949
  • 1973  (480)
  • 1971  (500)
  • Physics  (980)
  • 101
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2311-2314 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It was found that the strain-at-break plotted against strain rate of poly(2-hydroxyethyl methacrylate) networks crosslinked to a low degree suggests in the region of low reduced speeds of deformation the presence of a maximum.This effect was related to the secondary maximum in loss compliance, J″, and explained by the long relaxation times of untrapped entanglements.
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  • 102
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2371-2376 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In measuring sinusoidal normal stress difference of concentrated polymer solutions in a Weissenberg rheogoniometer, the resistance to motion of the upper platen due to the sample between the cone and plate should be taken into account. Correction terms are derived. The theoretical predictions of Lodge and others concerning the relationship between oscillatory normal stress difference and oscillatory shear stress are found to agree with experimental data if these corrections are applied.
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  • 103
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2453-2466 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Macroscopic thermal expansion in the chain direction has been measured for the first time on organic polymeric single crystals. Negative linear thermal expansion coefficients αM are reported and related to chain torsional motion and equilibrium point-defect formation for a solid-state polymerized phase of 2,4-hexadiyne-1,6-diol bisphenylurethane (HDU) which contains crystallographically located interstitial dioxane and for a dioxanefree phase obtained by thermal annealing. Data for as-polymerized single crystals (which are probably of extended chain morphology) between -50 and 100°C give αM = -(1.686 ± 0.039) × 10-5 - (1.35 ± 0.18) × 10-7 t with t in °C. During volatilization of 11.7 ± 1.0 wt-% interstitial dioxane and a resulting crystal structure change, the as-polymerized fibers fibrillate and shrink irreversibly by 0.16 ± 0.04%. Although dichroism and diffraction measurements indicate both a high degree of crystallinity and chain alignment for the dioxane-free phase, the average thermal expansion coefficient, (-3.0 ± 1.0) × 10-6 °C-1 between -50 and 150°C, is about an order of magnitude less than for the as-polymerized single crystals.
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  • 104
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2307-2310 
    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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  • 105
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2339-2356 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new theory, which relates viscous drag reduction to the energy stored by polymer molecules subjected to a fluctuating wall shear rate, is proposed for the origin of the Toms effect. The strain energy densities of several polymer solutions were estimated from bead-spring theory. The requisite molecular polymers were optimized by a least-squares fit of calculated to observed intrinsic viscosities. Friction reduction was found to be a monotonic function of the strain energy density for a given polymer-solvent combination. The correlation was independent of molecular weight and concentration for pipes of 0.5-2.0 in. diameter. Differences between the points of onset of drag reduction for different polymer-solvent combinations may be due to the unequal effect of internal viscosity.
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  • 106
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2403-2411 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The molecular conformation and the crystal structure of α-form poly-p-xylylene has been determined by x-ray diffraction. The polymer has a monoclinic unit cell with a = 5.92, b = 10.64, c (fiber axis) = 6.55 Å, and β = 134.7°. Two chains pass through the unit cell, and the space groups is C2/m. The packing fraction is 0.705. One monomer unit makes up the fiber identity period and the internal rotation angles are 0° and 90° for the —CH2—CH2— and —CH2—φ— bonds, respectively. All benzene rings are in parallel orientation, perpendicular to the ac plane.
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  • 107
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2441-2451 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: For a polymer in which permanent rupture of individual molecules is the rate-limiting process for plastic deformation, the kinetics of chain-end diffusion and secondary radical reactions should be compared with the kinetics of caged radical recombination in the calculation of activation parameters for plastic deformation. If mechanisms of cage escape are slower than those for cage recombination, the activation parameters for plastic deformation will differ from those for the initial bond-breaking process. For the case of polyethylene deformed in the vicinity of 250°K, the critical thermally activated event appears to involve scission of the polymer molecule near the site of an abstracted hydrogen atom. For this system the dominant cage-escape mechanism is diffusion, which is faster than either hydrogen abstraction or unzipping to the monomer. However, at low stresses the rate of cage recombination is expected to be higher than the rate of cage escape, so that the activation parameters for deformation should be the sum of those for chain scission and diffusion. The contribution of diffusion (ca. 15 kcal/mole) to the activation energy for deformation (E*, extrapolated to zero stress conditions) is relatively modest. However, the calculated molar activation volume for deformation V* increases by almost an order of magnitude, i.e., from ca. 10 to ca. 76 cm3/mole when diffusion is required. Consideration of experimental values of E* and V* for high molecular weight polyethylene indicates that, in the regime examined, chain scission plus chain-end diffusion is required to effect plastic deformation.
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  • 108
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2489-2491 
    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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  • 109
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1375-1383 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Mean-square unperturbed dimensions 〈r2〉0 and dipole moments 〈μ2〉 have been calculated for propylene-vinyl chloride copolymers by means of rotational isomeric state theory. The calculations indicate that for these chain molecules 〈mu;2〉 is much more sensitive to chemical sequence distribution than is 〈r2〉0, a conclusion in agreement with results of previous studies of ethylene-propylene copolymers and styrene-substituted styrene copolymers. In the case of propylene-vinyl chloride chains, both 〈r2〉0 and 〈μ2〉 are most strongly dependent on chemical sequence distribution in the case of copolymers which are significantly syndiotactic in stereochemical structure. At equimolar chemical composition, increase in average chemical sequence length generally increases 〈r2〉0 but decreases 〈μ2〉. Under some conditions, values of these statistical properties go through a minimum with increase in the reactivity ratio product r1r2, thus complicating the use of experimental values of these properties in the characterization of chemical sequence distributions in these copolymers.
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  • 110
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1-14 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A homologous series of aliphatic polyoxamides, nylon 122, 102, 82, and 62, were prepared by the bulk polycondensation of dialkyl oxalates with diamines. Infrared spectroscopy, x-ray diffraction, differential thermal analysis, thermogravimetric analysis, and gas chromatography were used to study the structure and thermal stability of these polyoxamides. From the fiber pattern of nylon 122, a structural repeat distance of 19.5 Å was measured. This was in close agreement with the expected value for an extended planar, zigzag chain conformation. With the exception of the expected decrease in the structural repeat distance along the chain axis resulting from the different number of methylene groups, nylons 122, 102, and 82 were isostructural. Nylon 62 appeared to pack in a similar manner to the other materials studied. However, there were differences in the diffraction pattern of this polymer; these may be indicative of a different chain conformation or of strain in the crystalline regions of the polymer. The infrared spectra indicate the presence of strong hydrogen bonding in all the polymers. Thermal analysis and pyrolysis data revealed catastrophic polymer degradation between 400 and 500°C in nitrogen, with appreciable homolytic cleavage of the oxamide group.
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  • 111
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 25-30 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It is shown that an optically excited current in polyethylene does not interact with the dark absorption current. This implies that the carriers are different for the two processes. We suggest that holes are photo-injected and traverse the full thickness of the specimen, while the absorption currents are due to surface barrier processes, as proposed by other workers.
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  • 112
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 15-24 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Thermodynamic interaction parameters have been calculated from gas-liquid chromatographic measurements for linear and branched polyethylene interacting with selected hydrocarbons. The values of the interaction parameter χ are substantial in spite of chemical similarities between the polymer and low molecular weight hydrocarbon species, a fact attributed to significant differences in the respective thermal expansion coefficients. A systematic increase of χ is observed in going from branched to linear polyethylene systems. The thermal expansion coefficients of these polymer homologs therefore may not be identical. The present χ values differ substantially from those reported in earlier literature. The comparison confirms suspicions that some older data, based on equilibrium sorption experiments, were erroneously low because of an underestimate in the reduced melting temperature of polymer in the presence of excess solvent.
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  • 113
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 31-42 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: By means of electron microscopy of surface replicas and both small-angle and wide-angle x-ray scattering, nylon 6 fibers were investigated in the as-spun state, after drawing at 180°C to a draw ratio up to 4.95, and after subsequent annealing. As spun, the fiber exhibits a small fraction of row-nucleated cylindrites and a great many spherulites (with an average diameter of a few microns) side by side. Drawing deforms the spherulites into spindle-shaped structures (λ = 2) and subsequently produces well-aligned microfibrils. Small-angle x-ray scattering yields a two-point diagram at small λ and a fourpoint diagram at high λ. The long period seems to decrease slightly with draw ratio. Annealing at temperatures above the temperature of drawing increases the long period to a greater extent with samples of lower λ. The crystal lattice orientation is nearly complete at λ = 4.95.
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  • 114
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1803-1815 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Solution properties of poly[1(2-hydroxyethyl)pyridiniumbenzene sulfonate methacrylate] and poly[1(2-hydroxyethyl)trimethylammoniumbenzene sulfonate methacrylate] were studied. Within a certain concentration range of some added low molecular weight electrolytes, phase separation occurs. The dependence of intrinsic viscosity on molecular weight was determined and the steric factor estimated for both polymers. For nonaqueous solvents, an extrapolation of the dependence of the refractive index increment of the polymer on the refractive index increment of the polymer on the refractive index of the solvent leads to an apparent refractive index of the polymer, different from the refractive index determined directly by the immersion method. Some peculiarities of light scattering in solutions with no electrolyte added are mentioned.
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  • 115
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1841-1848 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The application of laser-Raman spectroscopy to the analysis of copolymers of glycidyl methacrylate (GMA) with methyl methacrylate (MMA) and styrene is discussed. For both copolymer systems the line near 1451 cm-1, assigned to the methylene bending mode, was found to be a useful reference. Lines characteristic of each monomer were identified. The intensities of these lines were found to be linearly related to the composition of the copolymers when normalized against the 1451 cm-1 reference. The line near 1730 cm-1, assigned to the carbonyl stretching mode, was also found to be a useful reference for the copolymers of methyl methacrylate and glycidyl methacrylate.
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  • 116
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 117-135 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The nucleating activity of a large number of nucleating agents for the crystallization of polyolefins is not based on a high surface free energy of the substrate or on epitaxy, or on a minimum particle size just compatible with the thickness of the crystallizing polymer lamellae, or on any persistance of crystalline material in holes of the nucleating particles. The relevant mechanism is thought to be nucleation at steps of limited length in the surface of the nucleating particles. The nucleation is enhanced by a high degree of accommodation of polymer molecules at the surface of the substrate through the presence of ditches in the latter which cause prealignment of polymer chains and thus facilitate crystallization.
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  • 117
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Analytical expressions are derived for the concentration dependences of different apparent average (n,w,z) molecular weights for two types (end-to-end and segment-to-segment) of open association of polymolecular unimers. The open association is defined as an association leading to an unlimited number of multimer species. The type of association depends upon the number of associogenic sites per unimer molecule: for the end-to-end type this number is constant, whereas for the segment-to-segment type it is proportional to the degree of polymerization of the unimer. For the end-to-end association, a simple relation exists between the polydispersity (M̄r)w/(M̄r)n of the mul-timer and the association number r and the polymolecularity (M̄I)w/(M̄I)n of the unimers: (M̄r)w/(M̄r)n = 1 + r-1[(M̄I)w/(M̄I)n - 1]. The z-average and higher averages of the r-mers may be lower than the corresponding averages of the unimers. In the theta-state, (M̄n)app,Θ and (M̄w)app,Θ are linear functions of c/(M̄n)app,Θ, whereas a more complicated relation exists for the apparent higher averages. For the segment-to-segment association, both (M̄w)app,Θ and (M̄z)app,Θ are linear function of the weight concentration c, whereas no closed expression could be found for (M̄n)app,Θ. For the polydispersities of multimers one finds (M̄I)z/(M̄r)w = 1 + r-1[(M̄I)z/(M̄I)w - 1], and, in the special case of a Schulz-Zimm distribution of unimer molecular weights, (M̄r)n/(M̄r)w = 1 + r-1[(M̄I)n/(M̄I)w - 1].
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  • 118
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 175-191 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The complex dielectric constants ∊* = ∊′ - j∊″ of each of several members of a system of copolymers of 4-chlorostyrene and 4-methylstyrene have been measured from 1.6°K to 300°K and from 0.1 kHz to 20 kHz. The principal experimental findings are: the strength of the relaxation process which occurs near 50°K at 1 kHz varies linearly with changing copolymer composition; both the apparent activation energy (H = 2.7 ± 0.7 kcal/mole) and the shape of the relaxation curve are independent of the composition variable and of the temperature (or frequency) within the ranges studied; and the ratio of the relaxation strength of poly-4-methylstyrene to that of poly-4-chlorostyrene in the 50°K process is about 25 times the corresponding ratio for the primary relaxation process that occurs in the neighborhood of the glass-transition temperature. These findings suggest that in the 50°K process the phenyl groups relax independently of one another; that the apparent activation energy and the shape of the relaxation spectrum are determined primarily by the nature of the intrachain forces; and that the strength of the relaxation process depends primarily on effects of intermolecular forces that are governed by the molar “free volume” of the copolymers.
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  • 119
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The molecular orientation behavior of regenerated cellulose, in both crystalline and noncrystalline phases, was investigated quantitatively under various conditions during coagulation-regeneration from viscose solution and during drying of the resulting gel film. It was concluded that the stronger the tensions which arise parallel to the film surface during coagulation-regeneration and drying of the gel film, the more prominent become the uniplanar orientation of the (101) crystal plane and planar orientations of the crystal b axis and noncrystalline chain segments, all parallel to the film surface and associated with considerable distortion and disintegration of the regenerated crystal. This conclusion suggests an orientation mechanism of the cellulose II crystal, namely, rotation of the crystal around the U(101) axis associated with slippage of the (101) crystal plane, the most highly hydrated and most readily dislocated plane, in the direction of the tension, which is also parallel to the surface of the film. The behavior of this type of uniplanar orientation of the (101) crystal plane is characterized semiquantitatively by comparing observed distributions of the orientation of crystallographic axes with those calculated on the basis of a relatively simple model for crystal orientation.
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  • 120
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2135-2142 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An attempt was made to evaluate stresses on chemical bonds in axially stressed polymers from the shift of skeletal vibration frequencies in chain molecules. The maximum stress on chemical bonds was found to be at least ten times the average stress on the specimen.
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  • 121
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2153-2171 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Specimens of poly(vinylidene fluoride), crystal form II, annealed at different temperatures between 130 and 180°C were characterized by specific volume measurements, differential scanning calorimetry (DSC), and electron micróscopy. The degree of crystallinity calculated from the specific volume changed only by 15% i.e., from 50% to 65%. On the other hand, the melting behavior changed with annealing conditions. When a specimen was annealed above 170°C, two endothermic peaks appeared on either side of the annealing temperature. Results from DSC measurements made at different heating rates and electron microscopy showed that the two endotherms were caused by a bimodal distribution of lamellar thicknesses. The equilibrium melting point was found to be 210°C from the linear relation of the melting point and the annealing temperature. The equilibrium enthalpy and entropy of fusion were found to be 1.6 keal/mole and 3.3 eu/mole of repeat units by measurement on polymer-diluent mixtures. The surface free energy was found to be 5.1 kcal/mole of lamellar sequences from the plot of melting point versus reciprocal lamellar thickness obtained by electron microscopy. From a plot of enthalpy of fusion versus reciprocal lamellar thickness the surface enthalpy was found to be 20 keal/mole of lamellar sequences. These data lead to the estimate that a chain fold consists of about 30 repeat units.
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  • 122
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 217-221 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Nylon 6 in the form of bundles of fibers or rods was treated to contain traces of chloranil of other quinones. When stressed within an EPR cavity, the radicals produced were trapped in a relatively stable form containing the quinone. This method offers a quantitative measurement of the integrated number of free radicals produced during a stress history.
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  • 123
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 233-248 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystal structure of α-gutta percha has been determined by x-ray diffraction. The unit cell parameters are a = 7.98 Å, b = 6.29 Å, c (fiber period) = 8.77 Å, and β = 102.0° (monoclinic). The space group is P21/c-C2h5. Two molecular chains of nearly trans-CTS-trans-CTS̄ conformation pass through a unit cell; C, T, S, and S̄ being the cis, trans, and two types of skew forms, respectively. The constrainedle astsquares method was modified so that the order of the least squares matrix could be reduced and was applied to the refinement of the crystal structure.
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  • 124
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 399-411 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The molecular weight distribution in various celluloses degraded with hydrochloric acid has been studied by gel-permeation chromatography. Measurements were made on the residue after hydrolysis, on the degradation products solubilized by the acid, and on whole degraded samples comprising the product soluble in the acid plus the residue. It is shown that the total number of crystallites decreases during hydrolysis while the chain length distribution remains constant. The crystallites are gradually broken down into molecular fragments which show a size distribution centered on species with a degree of polymerization of about 8. Possible interpretations of these results are discussed.
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  • 125
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 413-425 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The pH-induced conformational transition of maleic acid-styrene copolymer in aqueous NaCl solutions has been investigated by potentiometric titration, viscosimetry, and dilatometry. The dependence of the intrinsic viscosity on the degree of neutralization of the primary carboxyl group indicates that the transition is from a compact to a loosely coiled form. From titration data, the standard free energy change ΔG° per monomole, for the transition from the uncharged compact from to the hypothetical uncharged loosely coiled one is estimated to be about 370-280 cal/monomole for concentrations ranging from 0.0092 to 0.2739N in NaCl. The value of ΔG° decreases slightly with increasing temperature in the temperature range from 15 to 30°C. The volume change associated with the transition was found to be -0.6 ml in 0.01N NaCl and -0.9 ml in 0.09N NaCl per monomole, respectively. From viscosity data, changes of molecular dimensions and the long-range interaction parameter through the transition region have been discussed.
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  • 126
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 427-448 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Wide-line proton magnetic resonance spectra of thick (100 μ) and ultrathin (0.25 μ) membranes of cellulose acetate have been obtained in the “bone-dry” state and in the wet state up to 2.5% water by weight. The NMR spectra were recorded with the membrane face aligned parallel and perpendicular to the magnetic field direction. The first derivative spectra of wet thick membrane (above 0.4% water) show a sharp center peak and at least one broad outer peak, both in the parallel and perpendicular orientations. The spectra of wet ultrathin membrane, on the other hand, show a pseudodoublet in the perpendicular orientation and a broad singlet in the parallel orientation. The differences in the spectra of the thick and ultrathin membranes are discussed in terms of “free” and restricted water believed to arise from the differences in the structure of thick and ultrathin membranes.
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  • 127
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 449-456 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The monomeric diglycidyl ether of bisphenol-A cured with methylenedianiline has been studied by pulsed NMR. Values of the proton relaxation times T1, T1p, and T2 have been measured over the temperature range -160 to 200°C. The system was studied after being fully postcured at 180°C and after being cured at 100°C and at 54°C. The relaxation times are interpreted in terms of molecular motion in the cured resins, i.e., methyl group reorientation, segmental motions, and general molecular motion. The results are compared with those obtained previously by us for the uncured resin. Correlation frequencies for the segmental motions are compared with those obtained from dielectric relaxation and mechanical loss studies. There are at least two principal segmental motions present in the cured system, and the nature of these motions is found to depend on the cure temperature. These effects are discussed in terms of crosslinking and annealing of the system.
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  • 128
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 457-465 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An approximate model is developed which relates the twisting seen in the spherulitic crystallization of many materials to surface stresses. Expressions are presented for the twist period as a function of the surface stress. These are compared with previous experimental data on polyethylene and data on hippuric acid obtained in the present investigation. In both cases the experimental data are in accord with the predictions of the model.
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  • 129
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An examination of powder x-ray diffractograms of native and hydrolyzed cellulosic materials obtained from widely different sources revealed the presence of materials having a higher degree of molecular order than ramie hydrolyzate, the conventional crystalline standard for cellulose. With the use of these materials as new crystalline standards, a critical reappraisal has been made of the validity of the application of the two-phase (i.e., fringed-micelle) hypothesis to the fine structure of cotton and related cellulosic materials. It is concluded that the lattice structure of cotton and related celluloses of plant or bacterial origin is liquid-like or paracrystalline.
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  • 130
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 467-486 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In order critically to evaluate the previous morphological interpretations of stress relaxation during oriented crystallization, a reexamination was made of the relaxation behavior of the same oriented natural rubber material used for the x-ray investigation in Part II of this series. Our results were found to be in qualitative agreement with previously published reports. Comparison of stress-relaxation rates at low temperatures for samples with strains of 200% or more with crystallization rates at room temperature by others for similar elongations indicates a dual nature in the strain-induced crystallization process. This conclusion is in full agreement with the indication of dual crystalline morphologies, namely, fibrillar and lamellar, for both electron microscopy and x-ray investigations on highly stretched samples reported in Parts I and II. Examination of stress-relaxation data in light of morphological evidence for oriented crystallization indicates that caution must be exercised in attaching morphological significance to the Avrami exponent n obtained from stress-relaxation or crystallization data.
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  • 131
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 511-527 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Although samples of amorphous polymers cast from solution are usually assumed to be isotropic, they may, in fact, have some anisotropy due to the Bénard effect, in which the convection currents produced by evaporation are organized into a regular arrangement of cells. A pattern of hexagonal convection cell is easily visible during casting of SBS triblock copolymers. The anisotropy is demonstrated by comparing the small-angle x-ray diffraction diagrams taken through the face and edge of the films. The domain structures in two SBS copolymers are characterized by diffraction measurements. The smallangle diagram of a triblock polymer containing 50% styrene indicated a lamellar structure, while that from a 28% styrene copolymer is interpreted as arising from a hexagonal array of polystyrene cylinders dispersed in a continuous polybutadiene phase. Published diffraction data for block copolymers and other amphiphiles are surveyed in an attempt to place some limitations on the composition ranges over which the various types of domain structure exist. The factors which determine the dimensions of the two domains in lamellar phases formed from diblock copolymers are examined theoretically, and the predicted dimensions are compared with experimental results.
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  • 132
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 499-510 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The partial molar excess free enthalpies and enthalpies as well as the molar excess enthalpies of a number of n-alkane systems were reexamined within the scope of the polymer solution theory of Flory, Orwoll, and Vrij and that of Prigogine in the version after Delmas, Patterson, and Somcynsky. A semiempirical method was used to obtain characteristic n-alkane data, which obey the principle of corresponding states. By using these data (instead of those from the partition function after Flory and collaborators), a physically realistic interpretation of the excess free enthalpies over the whole concentration range is possible if the combinatorial contribution is purely athermal in nature. Both theories give an enthalpy interaction parameter near zero as expected, whereas neither a significant end effect nor an entropic interaction contribution is apparent from the analyses of the excess free enthalpies. The poor results obtained for the partial excess enthalpies and the enthalpies of mixing reflect the inadequacy of the partition functions on which these modern solution theories are based.
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  • 133
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 529-538 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A method based on use of NMR and infrared spectroscopy is described for the quantitative determination of the structural units generally occurring in polyalkenamers. The possibilities offered by both techniques are pointed out: in particular, the values found for the absorptivities of the infrared bands typical of unsaturated alkenamer units are extensively discussed.
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  • 134
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 539-548 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The linear viscoelastic and stress-strain behavior of poly(n-butyl methacrylate) networks at a content of crosslinking agent (ethyleneglycol dimethacrylate) of c—0-1 × 10-4 mole/cm3 was investigated in the main transition and rubberlike region in the temperature interval from 20 to 150°C. The dependence of the unperturbed chain dimensions on temperature was determined from thermoelastic measurements in the rubberlike region; this dependence was unaffected by the content of crosslinking agent. Application of time-temperature superposition to the linear viscoelastic behavior did not give a continuous superimposed curve in the proximity of the rubberlike region; superposition within the whole time region required introducing the change of the unperturbed chain dimensions with temperature. This correction was sufficient for a sample with a higher content of the crosslinking agent. However, for loose networks (c〈 0.1 × 10-4 mole/cm3) it was insufficient, because of another relaxation mechanism in the region of high temperatures. It was found that the intensity and temperature dependence of this relaxation mechanism, which is probably due to a change of the number of entanglements with temperature, are connected with the magnitude and the temperature dependence of the C2 constant of the Mooney-Rivlin equation.
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  • 135
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 549-558 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Numerical calculations were performed for the viscoelastic properties of dilute solutions of branched star polymers with equal branch lengths as formulated in terms of a bead-spring model by Zimm and Kilb without using the integrodifferential equation approximation method to calculate the eigenvalues. The complex modulus and complex viscosity were calculated as functions of frequency for various combinations of the number of branches f (4, 8, and 13), the number of beads in one branch Nb (= N/f; 20 to 100, where N + 1 is the total number of beads, N the number of springs in the molecule) and the reduced hydrodynamic interaction parameter h* (= h/N1/2 0.05 to 0.3, where h is the hydrodynamic interaction parameter of Zimm and Kilb). The frequency dependence of the complex modulus in the low-frequency range depends mainly on h* and not on Nb if Nb is large enough, and it is very close to that calculated from the eigenvalues for h→∞ obtained by Zimm and Kilb, if h* is about 0.25. As h* decreases from 0.25, the frequency dependence gradually approaches that of the free-draining cash (h→0). Calculations may be carried out for h* values somewhat larger than 0.25 and result in a frequency dependence that is not intermediate to the h → 0 and h → ∞ cases as evaluated by Zimm and Kilb. The physical meaning of such “super-non-free-draining” values of h* is uncertain, however. The intrinsic viscosity ratio g′ = [η]f/[η]lin is an increasing function of h* and changes very slowly with N. For h* = 0.25, g′ is close to the non-free-draining limit for any value of N.
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  • 136
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 559-569 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A method for determining long-chain branching frequency and molecular weight averages for unfractionated low-density polyethylene (LDPE) by the combined use of gel-permeation chromatography (GPC) and intrinsic viscosity data has been reported (GPC-IV method). The method assumes that the number of long branches λ per unit molecular weight is a constant independent of molecular weight. Recent data reported on λ as a function of molecular weight M in commercial LDPE indicate that this assumption is not generally valid, and concern has been expressed as to the size of the errors in molecular weights calculated using this assumption. The errors associated with assuming that λ is constant were evaluated in this study by first determining the way in which λ varies with M for two typical commerical LDPE resins by fractionation and application of the GPC-IV method to representative fractions. The experimentally determined relations between λ and M were then employed in the calculation of molecular weight and molecular size averages from GPC-IV data on the original unfractonated samples. Although it was found that λ increases with molecular weight for both samples, the results indicate that the error involved in assuming that λ is a constant is no greater than the precision with which molecular weight averages can be evaluated by GPC.
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  • 137
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 571-585 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An x-ray study has been made of the structure of a series of ethylene-phosphonic acid copolymers and the parent low-density polyethylene from which they were derived. The phosphonic acid contents (groups per 100 carbon atoms) of the copolymers were: A, 0.8; B, 1.8; C, 2.8; and D, 8.0. Small-angle x-ray scattering (SAXS) results show that the phosphonic acid substituents do not incorporate into the crystal lattice to any appreciable extent, that the substituents have the effect of decreasing the average thickness of the crystal lamellae and increasing the breadth of the size distribution of thicknesses, and that a two-phase model does not adequately account for the observed SAXS invariant. Wide-angle x-ray scattering (WAXS) results show that specimens, A, B, and C are partially crystalline with the polyethylene crystal structure and that D is amorphous. The observed broadenings of the 110 and 200 crystal reflections in the copolymers indicate that the substituents decrease the lateral dimensions of the crystalline lamellae and/or increase the deformation of the lattice due to external strain. Specimen D, completely amorphous according to the WAXS criterion, exhibits the largest value of the SAXS invariant of all the copolymers studied and must thus possess a multiphase structure consisting of small ordered regions and a disordered phase. The results of the study show the structure of the copolymers to be consistent with the fringe-micelle model but do not rule out the folded-chain model, although a regular fold surface is unlikely.
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  • 138
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 663-681 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Permeability, solubility, and diffusion coefficients have been determined for halothane (CF3CHClBr) and methoxyflurane (CHCl2CF2OCH3) in silicone rubber at temperatures from 17 to 60°C and at relative pressures from 0.05 to 0.96. The solubility of both penetrants in silicone rubber is a strong function of penetrant concentration (or relative pressure), and can be represented satisfactorily by the Flory-Huggins relation with single values of the interaction parameter χ. The solubility coefficients decrease with increasing temperature at constant pressure. Mutual diffusion coefficients exhibit maxima when plotted against penetrant concentration; these maxima are attributed to the mass flow of polymer together with dissolved penetrant. Intrinsic diffusion coefficients increase linearly with increasing concentration. The energies of activation for diffusion are low, probably because of the ease of segmental motion about the Si—O linkage. The diffusivity data are examined in terms of Fujita's “free volume” model and of transition-state theory. Permeability coefficients for the two penetrants are large, of the order of 10-6-10-5 cm3(STP)-cm/(sec-cm2-cm Hg), and increase markedly with increasing concentration or decreasing temperature. This behavior is regarded as a consequence of the low energies of activation for diffusion.
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  • 139
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 635-661 
    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 previously proposed distributions of particle size and interparticle “gap” lengths on the small-angle x-ray scattering of a paracrystalline one-dimensional macrolattice has been examined. It was concluded that the general paracrystalline model, in which the fluctuations of crystalline and amorphous thickness both contribute to the destruction of long-range order, best describes the structure of lamellar aggregates in semicrystalline polymers. By using this model, the influence of symmetric and asymmetric lattice statistics on the positions of the scattering maxima were investigated. It was found that positively skewed thickness distributions result in the second-order maximum occurring at an angle greater than twice that of the first-order maximum (sx̄2/sx̄1 〉 2.0); the position of the first-order maximum is generally greater than the Bragg angle of the structure. With negatively skewed distributions, the ratio of the scattering angles, sx̄2/sx̄1, is less than 2.0, and the first maximum is displaced below the Bragg angle. Qualitatively similar behavior is found with lattices characterized by symmetric lattice statistics, though these deviations from the Bragg conditions are smaller than in the case of negatively skewed distributions. The ratio of the scattering angles of the second and first maxima best reflects the general shape of the lattice statistics in a paracrystalline lattice. The effect of a transition zone, having properties intermediate between those of the crystalline and amorphous regions, was also considered. While the intensity of the higher-order maxima is decreased, no significant shift of the scattering angles results from the incorporation of such a transition zone.
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  • 140
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 683-691 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A theory of the small-angle scattering of circularly polarized light from an anisotropic sphere has been derived. The validity of the theory has been verified, and a relationship between the structural information thus obtained and the structural information obtained with linearly polarized light has been demonstrated.
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  • 141
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 693-708 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An apparatus and procedures are described for the observation of the light-scattering changes during the periodic vibration of a polymer film sample. The relationship between static and dynamic scattering experiments is discussed as are the means for interpreting such experiments in terms of spherulite deformation and statistical theories. The performance of the apparatus is illustrated with some experiments on a medium-density polyethylene sample.
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  • 142
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 709-736 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dynamic light-scattering measurements are reported for a medium-density and a low-density polyethylene. It is found that the scattering at small angles can be described in terms of the deformation of spherulites, whereas that at larger angles depends upon rearrangements of partially ordered crystals within the spherulites.
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  • 143
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 875-897 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(vinylidene chloride) (PVDC) separates from the reaction mixture during the free-radical polymerization of vinylidene chloride. The morphology of the “as-polymerized” powder is determined by the degree of undercooling existing in the reaction medium at the time of crystallization. Crystallization occurs simultaneously in the process of polymerization and subsequently by the precipitation of polymer which formed in solution. As the medium becomes more favorable, an increasing portion of the polymer forms in solution and then crystallizes. The morphology developed by polymerization in borderline solvents such as dioxane can be nearly duplicated by recrystallization under similar conditions. The simultaneous occurrence of solution and solid phase polymerization leads to a double DTA endotherm. The upper peak at ca. 200°C represents the melting point of PVDC. The size and temperature of the lower peak vary with polymerization conditions. The results can be correlated with the degree of under-cooling as estimated by the difference between the polymerization temperature and the temperature at which the crystalline polymer dissolves in the reaction mixture.
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  • 144
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 899-907 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The sedimentation of an unperturbed polymer chain in dilute solution is reformulated by using Burgers' method, in which the no-slip boundary condition on the surface of each chain element is taken into account approximately. It is shown that the forcevelocity proportionality relation employed so far as the basis of theoretical developments in polymer hydrodynamics can be justified as a first approximation to the no-slip condition. The derived expression for the translational friction coefficient ft is a complex function of n and a/b, where n is the number of chain elements in a single molecule and a/b is the ratio of the Stokes radius of a chain element to the effective bond length. Three special cases corresponding mathematically to b = ∞ (no hydrodynamic interaction), a ≪ b (Kirkwood-Riseman theory), and b = 2a (touching-sphere model) are examined in detail. Finally, it is shown that when a/b = 0.2360, our ft varies linearly with n1/2 over the entire range of n.
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  • 145
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1975-1984 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Shear stress and first normal-stress difference of polyisobutylene dissolved in low molecular weight polybutene (concentrations 0.7 to 19 wt-%) were measured as a function of the shear rate. The dependence of viscosity η on shear rate \documentclass{article}\pagestyle{empty}\begin{document}$\dot \gamma $\end{document} was represented by the equation η = η∞ + (η0 - η∞)/(1 + α\documentclass{article}\pagestyle{empty}\begin{document}$\dot \gamma $\end{document}n) proposed by Cross, where the subscripts (0 and ∞) denote values at infinitesimal and infinite rate of shear, α is a constant associated with rupture of entanglement linkages, and n is a constant. The empirical value of n is 10/13 for 19% solution and 2/3 for the other solutions. The concentration dependence of α was roughly expressed as α = 104 c2.7, where c is the concentration in grams polymer per milliliter solution. The first normal-stress coefficient ψ12 can be represented by ψ12 = ψ12∞ + (ψ12∞ - ψ12∞)/(1 + β\documentclass{article}\pagestyle{empty}\begin{document}$\dot \gamma $\end{document}m). The analysis of data based on the equations shows that m = 2n and β ≈ α2. The steady-state compliance Je was calculated from the relation Je = ψ120/2(η0 - ηs)2, where ηs is the solvent viscosity. Je shows a maximum at about c = 0.03 and is directly proportional to c-2 in the higher region of c.
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  • 146
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2143-2152 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Based upon the high-temperature solid-state dielectric behavior of H-Film and supporting evidence from infrared spectroscopy, heat capacity, thermal expansion, and dynamic mechanical measurements, it is concluded that the actual chemical structure of H-Film is far more complex than previously expected. The very unusual thermal properties of this polymer, such as lack of a glass transition temperature, its extreme insolubility, and high dielectric losses above 250°C with only weakly corresponding mechanical losses, suggest that in addition to the pyromellitimide repeat unit, a significant part of the structure consists of amide groups, probably in the form of crosslinks.
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  • 147
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 991-1003 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Determination of important thermodynamic and physical properties of polymers has often been frustrated by the tendency of these materials to reorganize when heated. A novel technique has been developed which permits a more careful examination of the relationships existing between melting and morphology of single crystals. This has lead to the observation that high molecular weight polymers possess much narrower melting ranges than had been previously reported. By using this technique it has been possible to identify distinct transition temperatures for {100} and {110} fold sectors. DTA and DSC data have been previously reported for dried down single crystals. The applicability of this data to single crystals as they exist in suspension is questioned.
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  • 148
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 973-989 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Injection-molded specimens of polypropylene were examined by x-ray diffraction for texture and orientation patterns as a function of the distance from the surface and of molding conditions. At least three distinct layers in the surface region whose texture patterns differ and an isotropic core of the moldings have been identified. These layers show preferred orientations; the axes of symmetry of the oriented textures lie in a plane passing through the direction of flow and perpendicular to the mold surface, but are inclined to the mold surface at a small angle. Some of these layers may be missing in conditions of either very high or very low shear during the injection-molding flow. A tentative explanation of the formation of the texture patterns is proposed.
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  • 149
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 951-971 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A surface zone composed of at least three distinct layers has been detected in injection-molded polypropylene. The morphology of these layers as determined by optical and scanning electron microscopy forms a continuous picture from the “as-molded” surface to the core. With the exception of the first layer which is always featureless, the observed morphology is mostly spherulitic. Starting in the second layer, the spherulites decrease steadily in size until they reach a minimum somewhere near the middle of the third layer. After passing this point, they increase in size - rather rapidly - as the boundary between layer 3 and the core is approached. In samples prepared at the shorter fill times, the spherulites continue to decrease in size until they are replaced by the mixed matted straw-flat plate texture. The overall morphological features of this surface zone are explained by using an extension of a model for the crystallization of a quiescent polymer melt. In this model, growth originates from heterogeneous nuclei whose density varies throughout the sample as a function of both a temperature gradient and the induction time. Interpretation of anomalies in the fine structure of the individual layers indicates that shear is influencing the crystalline morphology also.
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  • 150
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1301-1318 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Heat capacity values for melts of polystyrene, poly(methyl methacrylate), polypropylene, and polyethylene are calculated on the assumption that the total constant-volume heat capacity Cv is made up of two parts: one associated with molecular vibrations, and one, with holes. Numerical values of both components are given for a wide range of temperatures and compared with experimental data. For poly-1-butene insufficient data for complete evaluation are available, so that only the vibrational contribution could be discussed.
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  • 151
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1319-1330 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The resistivity and dielectric constant for carbon black (5-12 vol-%) in a nonconducting matrix have been measured over the range 20-90°C and dc to 2-105 Hz. Styrene-butadiene rubber dissolved in tetracosane (22 parts SBR to about 70 parts wax) constituted the matrix. Wide variations in resistivity and dielectric constant with temperature and/or frequency were observed. A theory is presented to explain the experimental observations. It correctly predicts the qualitative features of the experimental results but its predictions are not quantitatively accurate.
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  • 152
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1293-1300 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: There have been several investigations dealing with the influence of the glass transition on the rate of radiation-induced reactions, especially the crosslinking reaction. On the other hand, no correlation has been reported between secondary transitions and the variation of a reaction rate. In the present work, the degradation of poly(methyl methacrylate) in the temperature range of -196 to 160°C has been studied. Two breaks in the Arrhenius plot were found. The first one is located at -5°C and can be correlated with the γ transition, which has been assigned to the hindered rotation of the ester group whose scission initiates the degradation. It is concluded that the thermal excitation of the bond rotation can either increase the scission rate or decrease the recombination rate of reactive intermediates by expanding the cage of the surrounding molecules. If the second mechanism occurs, the rotation of the α-methyl group should also be expected to favor the degradation. However, a second break in the Arrhenius plot was found at -130°C, and therefore significantly above the δ transition. The influence of this motion is therefore not clear. Certain radiation-induced reactions of poly(vinyl chloride), known from literature, seem to be influenced by a secondary transition. It is concluded that secondary transitions may be significant for scission reactions. This suggests, with respect to the known significance of the glass transition, that the various types of molecular motions in polymers may influence radiation-induced reactions.
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  • 153
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1465-1475 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Graessley's theory of non-Newtonian behavior of linear polymers is tested with data on polyethylenes and polypropylenes having a wide range of molecular weights and molecular weight distributions, and for a polyethylene fraction. Theoretical flow curves derived by using molecular weight distribution data from column fractionations are in good agreement with experimental curves obtained from a cone-and-plate viscometer and an extrusion-type rheometer, when the distribution is assumed to cut off at a maximum molecular weight. The experimentally obtained relaxation time for entanglement is found to be proportional to the Rouse relaxation time, though the former is about one decade smaller than the latter.
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  • 154
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1477-1488 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The isothermal crystallization of natural rubber was investigated under biaxial stretching. A marked planar orientation of crystals occurs in such a way that the (010) plane orients parallel to the film plane. The rate of crystallization increases with the biaxial stretching ratio, and the Avrami exponent n decreases. At the highest extension, n becomes less than unity. The equilibrium degree of crystallinity decreases with the stretching ratio. The crystallinity was less than 10% for the highest extension. The melting behavior is similar to that in uniaxial stretching.
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  • 155
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1535-1554 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Techniques have been developed for the prediction of tensile creep behavior of rubbery amorphous polymers with concurrent sorption or desorption of penetrant. The procedures require knowledge of polymer-penetrant interdiffusion behavior and the creep behavior of dry polymer and of polymer swollen to equilibrium. The techniques are based upon a moving boundary treatment, proposed by Kishimoto and Fujita, which has been modified and extended to consider two types of boundary definition, desorption in addition to sorption, and extension of the analysis to longer times. Calculated curves for the concurrent processes of diffusion and creep in the systems poly(n-butyl methacrylate) with ethanol, methyl ethyl ketone, or benzene vapors at 23°C agree to a good approximation with those measured directly. Diffusion coefficients calculated from the measured concurrent curves also are comparable with those measured directly in previous studies. The techniques are useful initial procedures which, with some further modification or extension, should lead to a more general description of concurrent mass and momentum transfer in polymer-penetrant systems.
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  • 156
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1585-1599 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystal structure of polychlorotrifluoroethylene has been studied. The pseudohexagonal lattice parameters are a = 6.438, c = 41.5 Å. The polymer chain is found to be helical with on the average 16.8 monomer units in one turn of the helix (equal to c). The skeletal angles on the CF2 and CFCI atoms are found to differ by 5 to 7 degrees. The polymer chain is found to accommodate these alternating angles by twisting around the axis of the helix. The result of the x-ray diffraction study agrees best with the assumption that the polymer is atactic with random position of the chlorine substituent. This randomness affects the microstructure of the polymer chain to such an extent that the diffraction effects are those of a system of continuous helices.
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  • 157
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1631-1640 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The ionic thermoconductivity (ITC) method has been used to study the α′ transition in the polyamide \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm \hbox{--}\rlap{--} [NH(CH}_{\rm 2} )_6 {\rm NH}\hbox{---} \rm CO(CH_2 )_4 {\rm CO\hbox{--}\rlap{--} ]}_{{\rm x}} $\end{document} (nylon 66). Depending on the thermal history of the sample, the maximum of the thermocurrent peak attributed to the α′ relaxation is found somewhere between ca. 45°C and ca. 66°C; on one heating, it shifts to higher temperatures. The high sensitivity and resolving power of the ITC method permit resolution of this peak into four elementary “pure” activated processes, with constant activation energies in the relevant temperature range. Each of the four corresponding relaxation times follows an Arrhenius law, with a well-defined characteristic temperature T0 = 83°C at which all these relaxation times are equal. When this last result is interpreted in the light of Eyring's or Bauer's theory, it gives a linear relation between “apparent” activation entropy and activation enthalpy of the elementary processes. The characteristic temperature T0 is independent of the thermal history of the sample, and the temperature shift of the thermocurrent maximum can be interpreted by the observed variation of the relative intensities of the elementary processes, without modification of their other characteristic features.
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  • 158
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1671-1682 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An understanding of the physical and chemical processes involved in the melt polymerization of polyesters in the higher inherent viscosity ranges is of fundamental importance in polyester preparation. For example, the volatile condensation product must diffuse to a polymer-vapor interface before polymerization can take place. Thus, the rate of polymerization of a polyester may be dependent not only upon the chemical kinetics of the polymerization reaction but also upon the diffusion of the condensation product through the polymer melt. The objective of the work presented in this paper was to determine to what degree diffusion or reaction kinetics, or both, limit the melt polycondensation of poly(ethylene terephthalate). Degrees of polymerization in melts between 0.0285 and 0.228 cm in depth at 270°C were measured for various reaction times and were compared with the predictions of mathematical models. The polycondensation rates under these conditions depend upon both the polycondensation rate constant k1 and the diffusivity D of ethylene glycol through the melt. Estimates of the values to these parameters are: k1 = 0.0500 (moles/mole of repeat unit)-1 sec-1; D = 1.66 × 10-4 cm2/sec.
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  • 159
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1867-1872 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dependence of the magnitude of the permeation flux on the sense of flow is studied in the case of a simple membrane laminate AB. The permeability of phase A is assumed to change from a low value at low permeant activity to a higher one at high permeant activity, whereas the permeability of phase B is constant. The results of the analysis of this simple system provide considerable insight into the factors influencing flow reversal effects in binary laminated membranes in general. The conditions under which marked effects of this kind are possible have been established.
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  • 160
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1873-1878 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dynamic mechanical properties of the ultrahigh molecular weight nylon 66 film and fiber produced by thermally induced solid-state polycondensation are presented. The α peak temperature of tan δ of these treated films and fibers is shifted 8-32°C higher than that of the appropriate control nylon 66 (film and fiber) while the maximum height of the tan δ peaks is decreased. The treated fibers have higher moduli at all temperatures (20-145°C) and humidities (30% RH) than do their control counterparts. The moduli of the treated fibers at 30% RH compare favorably with control yarn at 0% RH. These yarns also have a greater per cent of the 25°C modulus retention as temperature increases.
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  • 161
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1941-1948 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An expression for the flow field resulting from a time-dependent force with time-dependent point of action is derived from the linearized Navier-Stokes equations. The result is written as a sum of terms, the first of which is the “slow-change limit” corresponding to a stationary force acting at a stationary position. The application to the steady rotation of a dumbbell shows that this sum corresponds to a series expansion in powers of (L2|Ω|/v)1/2 where 2L is the length of the dumbbell, Ω is its angular velocity, and v is the kinematic viscosity of the liquid. It is pointed out that the results obtained are relevant to the problem of rotatory Brownian motion and to that of non-Newtonian viscosity.
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  • 162
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1963-1974 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The configurational statistics, i.e., the distribution of isotactic and syndiotactic placements, of binary vinyl copolymers possessing asymmetric α-carbon atoms is calculated for several sets of configurational parameters and three types of compositional statistics, i.e., Bernoullian, alternating, and blocklike. Terminal-model copolymerization is assumed with only the last monomer unit of the growing chain having a kinetic influence on the addition of monomers, but not preceding monomer units or their configurations. The configurational statistics of the copolymer chains is non-Markovian in general, which is in contrast to the first-order Markovian character of the compositional chain. The magnitude of the deviation of the configurational statistics from the Bernoullian and first-order Markovian distribution and the difference between configurational and compositional run numbers is evaluated. The degree of transcription of the compositional chain onto the configurational chain is discussed.
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  • 163
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2001-2012 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polarized infrared absorption spectra have been obtained by Fourier-transform spectroscopy for several crystalline and noncrystalline absorption bands of polyethylene crystallized by orientation and pressure in capillary viscometer. An analysis of data obtained at room temperature yielded degrees of crystallinity which are in good accord with values obtained from calorimetry and density measurements. The dichroism of the infrared absorption bands for the crystalline region revealed an extreme degree of orientation consistent with previous x-ray studies and also demonstrated that the degree of orientation is a good or better than that obtained from drawn polyethylene films with extension ratios of 20. Dichroism of bands from the amorphous phases revealed that the noncrystalline chain segments are in a comparatively relaxed state compared with results for drawn films having extension ratios of about 2 to 7. This is 1/10 to 1/3 the extension ratio of drawn polyethylene which shows maximum crystalline orientation. The results also indicated that the ratio of the GTG′ to GG segment conformations in the amorphous regions is larger than that of amorphous portions in unoriented polyethylene. The vinyl endgroups were shown to be highly oriented, while the main bulk of the amorphous polymer was fairly relaxed, i.e., of low orientation. It is concluded that the amorphous polyethylene state is strongly dependent on the nature of the crystalline-amorphous interface.
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  • 164
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2089-2098 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The sorption behavior of particulate-filled resin composites is discussed and related to several different models. A thermodynamic analysis of the sorption is presented in the form of a cycle for the changes in Gibbs free energy. From such an analysis it is possible to set up a scale of relative adhesion between filler and resin matrix. It is shown that the scale depends on the sorbate, but use of this scale will rate the adhesion between resin and filler in the correct relative order.
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  • 165
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2079-2088 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The glass transition in styrene-based ionomers was investigated by means of infrared spectroscopy and differential scanning calorimetry (DSC). Transition temperatures were determined from the temperature dependence of the peak absorbances of the 1700 and 1745 cm-1 bands. These transition temperatures agreed with glass transition temperatures (Tg) determined by DSC. With increasing degree of ionization, Tg and the enthalpy ΔH of the residual intermolecular hydrogen bonding increased. The values of Tg obtained were analyzed by the theory of Fox and Loshaek for the effect of crosslinks. It is concluded that sodium ions probably from ionic domains and act as crosslinks to reinforce the residual hydrogen bonding and may increase Tg. The absorbance at 1560 cm-1 (νCOO-) did not change at Tg. This suggests that the glass transition observed here is not due to the onset of the mobility in ionic domains, as has been proposed for ethylene-based ionomers on the basis of dielectric measurements.
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  • 166
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2123-2133 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements of apparent viscosity, normal stress coefficient, and storage and loss moduli have been used to determine the characteristic relaxation time. The ratio of the characteristic relaxation time θin corresponding to a given deformation rate ·γ to that of the initial state θe is found to be a function of ·γθin. For a wide range of polymeric systems, the ratio of normal stress to the initial high elasticity modulus and to the high elastic deformation γe are the same function of ·γθin. It has been established that γe, like other viscoelastic characteristics of polymer systems, is determined by the relaxation properties and their variation due to deformation. The dependence of γe on θe/θin is common to a wide range of polymeric systems. The generalized characteristics were independent of the nature of the polymeric chain, molecular weight, molecular weight distribution, temperature, polymer concentration in solution, and solvent type. These results allow us to describe approximately normal stresses and high-elastic deformations as functions of shear rate and storage and loss moduli as functions of frequency, if we know θin the relation between shearing stress and shear rate.
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  • 167
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2185-2197 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of energy calculations have been carried out in order to describe the epitaxial crystallization of polyethylene from solution in terms of molecular interactions. The total energy has been computed as the sum of electrostatic, dispersion, and repulsion contributions. The potential energy associated with a section of a planar-zigzag polyethylene chain has been determined for various orientations and positions above three different planar alkali halide substrates. Inspection of the energy surfaces as a function of the spatial degrees of freedom reveals that the minimum energy orientation of the chain is that for which it is parallel to the substrate [(001) cleavage plane] and aligned in the 〈110〉 direction on the surface, a result in accordance with available experimental evidence. Specifically, the chain preference is to position itself along rows of positive ions, whereas alignment along rows of negative charge appears energetically unfavorable. The mode of chain orientation is virtually independent of lattice matching criteria. Dispersionrepulsive forces have been found to be most sensitive to orientation and greater in magnitude than the electrostatic forces.
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  • 168
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2237-2252 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Proton-decoupled, partially relaxed, Fourier-transform NMR of 13C in natural abundance was used to determine spin-lattice relaxation times of individual carbons of polyisobutylene, polyacrylonitrile, poly(vinyl chloride), and poly(vinyl alcohol) in solution. It is shown that the relaxation times are independent of the difference in stereochemical configuration. From the values of the nuclear Overhauser enhancement factor it is shown that the relaxation times are independent of the difference in stereochemical configuration. From the values of the nuclear Overhauser enhancement factor it is shown that the excess spin energy from equilibration of all the 13C, even of quaternary carbons, in the polymers dealt with here is transferred to the lattice mainly through 13C-1H dipolar interactions. It is shown that the segmental motions responsible for the spin-lattice relaxation of the polymer skeleton in solution can be described by the isotropic model within a good approximation, except for poly(vinyl alcohol) at low temperature. The activation energies of skeletal and internal methyl motions are estimated from the temperature dependence of the correlation time. Differences in the 13C line widths for individual carbons of polyisobutylene are discussed briefly.
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  • 169
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2283-2289 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The mechanism of non-Newtonian behavior for flow from the lower to the upper Newtonian region is explained by a modification of Graessley's theory. In the theory proposed here, a viscosity ηfric, which is based on friction between polymer segments and is almost shear-independent, is introduced in addition to Graessley's entanglement viscosity ηent, which decreases with increasing shear rate. The theory is applied to previously obtained data on steady flow of polydimethylsiloxanes of different molecular weights. The agreement between calculated and experimental results is good. In polymers with the molecular weight above the critical molecular weight for entanglement Mc, the major contribution to viscosity near zero shear rate is ηent. As the shear rate increases, the flow curve has an inflection where ηfric cannot be disregarded in comparison with ηent. In the upper Newtonian region, ηfric has more influence on the viscosity than ηent. The theory can also explain the experimental results on flow of polymers with molecular weight below Mc, which were shown to be slightly non-Newtonian in the previous paper.
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  • 170
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1653-1670 
    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 linear polyethylene, prepared from a dilute xylene solution, were annealed below their melting temperature under atmospheric and 6 kbar pressure. In order to preserve the identity of the single crystals, they were suspended in an inert solvent medium, silicone oil and ethanol, during annealing. Examination of the annealed crystals under an electron microscope revealed development of numerous reorganization centers consisting of a central, elongated hole surrounded by a raised edge. Characteristics of these holes, especially their location and orientation, were interpreted in terms of the molecular packing that existed prior to the annealing and the mechanism of molecular reorganization that occurred during the annealing. The effect of high pressure was primarily to flatten out the crystals and to increase the number of reorganization centers, but the height of the raised edges remained about the same irrespective of the applied pressure. The present study also showed examples pointing to the importance of differentiating the annealing behavior of monolayer crystals from that of multilayer crystals.
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  • 171
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1703-1711 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The thermal degradation of four different forms of cellulose in nitrogen has been studied by using a thermobalance. In TG experiments a total weight loss at 900°C was 80% in the cases of film and pulp samples and 83% for two powder forms. The results for the isothermal degradation of the four samples at 270°C are plotted as degree of degradation α against reduced time t/t0.5 and compared with the master plots of Sharp, Brindley, and Achar. The experimental data fit most closely the plot for the Avrami-Erofeev equation in the form kt = {-ln (1-α)}1/n where n = 2. An activation energy of 144 kJ/mole has been found for the degradation of one of the celluloses from the results of isothermal runs at six different temperatures. It is postulated here that the thermal degradation occurs by random nucleation and nucleus growth in the cellulose fibrils so as to yield a carbon whose microporous structure is a replica of the pore system in the parent cellulose.
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  • 172
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1735-1745 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystallization of selenium from the melt has been studied as a function of time at 90, 126, and 200°C by following the density and the concentration of Se8 rings. The crystallization is shown to involve crystallization of the polymeric species in the melt and, especially at later stages of the crystallization, crystallization during polymerization. A kinetic scheme has been developed which permits the description of the experimental data.
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  • 173
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1769-1777 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The relative rates of relaxation and creep in shear, elongation, and isotropic compression are discussed in terms of the theory of linear viscoelasticity. Exact expressions are given for the creep rates; for the relaxation rates approximations are found which are useful in the glassy range where the amount of relaxation is small. Among the results of interest is the relation: \documentclass{article}\pagestyle{empty}\begin{document}$$ 1 \le {{\frac{{d\ln J}}{{d\ln t}}} \mathord{\left/ {\vphantom {{\frac{{d\ln J}}{{d\ln t}}} {\frac{{d\ln D}}{{d\ln t}}}}} \right. \kern-\nulldelimiterspace} {\frac{{d\ln D}}{{d\ln t}}}} \le \left[{1 + \frac{{B\left(t \right)}}{{3J\left(t \right)}}} \right] $$\end{document} valid if d In B/d In t is less than d In J/d In t as is intuitively expected and experimentally found. Here J(t), E(t), and B(t) are the shear, tensile, and bulk creep compliances, respectively. For polymers in the rubbery and flow regions, (d In J/d In t)/(d In D/d In t) is very close to 1(usually within 0.01%); in the glassy region, it is unlikely to be greater than 1.2.
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  • 174
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 109-116 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A model containing two rate constants is presented for the development of spherulites from sheaves. One, GR, is a radial spherulite growth constant while the other, GS, describes the rate of increase of apex angle of the sheaf. On the basis of this model, Avrami kinetics are developed which predict a change in the Avrami constant n from 5 to 3 as the sheaf develops into a spherulite. HV light-scattering patterns are calculated according to this model and are found to compare favorably with those found during the early stages of the crystallization of poly(ethylene terephthalate).
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  • 175
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 95-108 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Block copolymers having poly(tetrachlorobisphenol-A adipate) (PTBA) and polystyrene (PS) sequences were synthesized were synthesized by photodegradation of an oxime-containing polyester in the presence of styrene. Crystallinity, melting behavior, and spherulitic growth rates were studied as a function of block compositions and molecular weights. A model was proposed based on a complete phase separation between the two components. The influence of the polymer composition on the spherulitic growth rate is described by introducing a supplementary pre-exponential factor into the equation for the growth rate. This parameter is a measure of the tortuosity of the actual path that has to be covered owing to the presence of the noncrystallizable blocks.
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  • 176
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1859-1861 
    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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  • 177
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1879-1890 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The critical strain εc for crazing of polystyrene in each of a variety of organic liquids has been measured along with the degree of swelling of the polymer by the liquid and the attendant reduction in the glass transition temperature Tg of the polymer. The critical strain for the crazing in air and the Tg of each of a set of specimens molded from mixtures of o-dichlorobenzene and polystyrene have also been determined. Correlations of εc with Tg in the two cases are identical within experimental error for the first 40°C of Tg reduction; these results imply (1) that organic liquids do not exercise a significant surface energy role in solvent crazing and (2) that their only roles are associated with flow processes. Correlation of solvent crazing εc with solubility parameter of the crazing fluid is very poor for several reasons that are discussed.
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  • 178
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1891-1939 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dynamic x-ray diffraction and dynamic birefringence techniques are employed to determine the nature of the molecular motions associated with the α mechanical loss processes for low-density polyethylene. The results indicate that the low-temperature part of this loss (designated α1) is associated with an interlammellar “grain boundary” slip process while the higher temperature process (α2) involves intracrystalline motion and plasticity of the crystal itself. The activation energy for α1 determined by x-ray response is 25-30 kcal/mole, while that for α2 is 30-60 kcal/mole. The findings are consistent with dynamic infrared and dynamic light-scattering results which indicate that the motion of amorphous chains is closely correlated with that of the crystals. The relative contributions of amorphous and crystalline regions to the birefringence are dependent on the thermal treatment of the sample. The effect of static strain on the dynamic response indicates that crystal orientability is first increased with strain, probably because of splaying apart of lamellae, is subsequently decreased because of the restrictions of interlamellae tie chains, but then increases again as the spherulites are destroyed at high strain. The static strain reduces the orientability of amorphous regions.
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  • 179
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 1985-2000 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Molecular and crystal structures of poly-1,3-dioxocane and poly-1,3-dioxonane, the polyformals [—OCH2O—(CH2)m—]m with m = 5 and m = 6, respectively, are analyzed. Poly-l13-dioxocane is triclinic, space group with m = 5 and m = 6, respectively, are analyzed. Poly-1,3-dioxocane is triclinic, space group (fiber axis) and N (number of chains per unit cell) = 2. Poly-1,3-dioxonane is orthorhombic, (fiber axis) = 18.8 Å, and N = 2. The molecular conformations are roughly where T, G, and G are the trans, and the two gauche forms, respectively.
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  • 180
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2027-2037 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A model incorporating reversible, bimolecular immobilization for diffusion and sorption in glassy polymers is developed. Sorption is considered to occur by two distinct mechanisms: ordinary diffusion-controlled sorption and sorption resulting from the immobilization of diffusing gas molecules by prexisting sites in the polymer. Expressions are obtained for equilibrium sorption, transient sorption, and time lag. The effects of kinetic parameters of the model are illustrated and discussed.
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  • 181
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 149-173 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The theory of small-angle light scattering was developed for oblique incidence of the light beam on the surface of a two-dimensional spherulite. Results of the theory were compared with previously reported results of light scattering from two-dimensional and three-dimensional spherulites for normal incidence, and with some experimental patterns. The comparisons suggest that the scattering intensity distributions of two-dimensional spherulites deviate from those of three-dimensional spherulites when the sample surface is tilted with respect to the propagation direction of the incident beam, although they are almost identical when the sample surface is normal to the incident beam. Observation of the change of scattered intensity distributions upon tilting the samples thus provides a method of distinguishing between two-dimensional and three-dimensional spherulites. Moreover, this observation makes it possible to determine the degree of planar orientation of the optic axes of optically anisotropic scattering elements within two-dimensional spherulites. The calculations were carried out for special cases of two-dimensional spherulites with the optic axis orientation confined to the two-dimensional plane and randomly or helicoidally rotated around the spherulite radii.
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  • 182
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 193-200 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Previously it was found that the lamellar thickness of solution-grown polyamide crystals as assessed by low-angle x-ray diffraction appeared to be unaffected by crystallization conditions. This point has now been re-examined in detail on nylon 6.6 with crystallization temperature Tc as the main variable. Over a very wide range of Tc the lamellar thickness was invariant; a notable increase could be produced only at the highest Tc. The “invariant” lamellar thickness occurs at larger supercoolings than can be realized in the much-studied polyethylene, which may explain why it has not yet been reported for polyethylene. The existence of this minimum invariant value raises important questions concerning the applicability of the current kinetic theories over such a wide range of supercoolings. Several other polyamides also revealed invariant long spacings after crystallization from solution. This provides the justification sought for comparing, in the paper which follows, the long periods observed for a large number of polyamides.
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  • 183
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 223-232 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Craze initiation and propagation near a Griffith crack were studied in poly(methyl methacrylate) and polycarbonate. Craze propagation results either in eventual catastrophic failure or in termination of propagation. Photoelastic observations indicate that high stress concentration at the initial crack tip is relieved immediately after craze initiation and craze propagation introduces no new stress concentration at the craze front. These results lead to the conclusion that the criteria for craze initiation and propagation are described fairly well by the stress intensity factor. A fracture mechanics model proposed by Marshall et al. can explain the kinetics of craze propagation in poly(methyl methacrylate). However the growth rates are lower in polycarbonate than in poly(methyl methacrylate). This is attributed to the difference in a penetrant activity.
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  • 184
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 249-264 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Melting points and lamellar thicknesses have been measured for ethylene oxide-propylene oxide block copolymers (sym-PEP) with central poly(ethylene oxide) block lengths of 70-100 chain units and end poly(propylene oxide) block lengths of 0-30 chain units. Melting points of the block copolymers are lower than those of the corresponding poly(ethylene oxide) homopolymer by an amount (up to 15°C) which increases as the poly(propylene oxide) block length increases. Most samples have more than one melting transition, which can be assigned to variously folded chain crystals. End interfacial free energies σe for the various crystals have been estimated by use of Flory's theory of melting of block copolymers. For a given crystal type (e.g., once-folded-chain) σe is higher the longer the chain length of the end poly(propylene oxide) blocks. For a given copolymer σe is lower, the more highly folded the poly(ethylene oxide) chain.
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  • 185
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 265-268 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Melting points have been measured for several ethylene oxide-propylene oxide block copolymers (sym-EPE) chosen from the Pluronic range. Melting points of the block copolymers are lower than those of the corresponding poly(ethylene oxide) homopolymer by up to 4°C. The melting point depressions are much smaller than those observed for comparable sym-PEP block copolymers.
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  • 186
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 269-273 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dependence of joint strength upon the molecular weight between crosslinks Mc of an adhesive has been investigated for joints which consist of a crosslinked, amorphous rubber adhering to a rigid polymeric substrate. The joint strength was found to be independent of Mc if results were compared at the same effective rate of testing. If, however, values of joint strength were compared at a particular test temperature and rate, the joint strength generally increased as the value of Mc decreased. This result can be explained by the increase of the glass transition temperature of the adhesive with increasing crosslink density.
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  • 187
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 359-368 
    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 structural defects present in crystalline polymers and the molecular structure of the drawn material is studied by drawing fibers from irradiated polyethylene single crystals. Irradiation introduces a structural defect in the crystal lattice since it generates crosslinks preferentially, the density of which is controlled by the radiation dose. Observations by means of transmission electron microscopy and electron diffraction indicate that fiber drawing occurs by breaking off of single blocks of folded chains and by subsequent thermally activated rearrangement of the molecules in the drawn material. With increasing crosslink density the size of the blocks decreases, and the fibers become increasingly interconnected so that a network of fibers is formed. If the dose is about 10 Mrad, the crosslinks present in the crystals result in the formation of bundles of fibers. Above 35 Mrad the formation of fibers (single fibers as well as bundles) ceases, and the drawn material forms a thin (15 Å), continuous film. The observed change in morphology with increasing dose (crosslink density) is interpreted in terms of the additional bonding forces between adjacent chains due to crosslinks.
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  • 188
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 391-392 
    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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  • 189
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 389-390 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 190
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 369-388 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: One of the cyclic oligomers of formaldehyde, 1,3,5,7,9,11-hexoxecane, was found to undergo polymerization in the solid state to form polyoxymethylene both during and subsequent to x- or γ-irradiation. The polymer yield increases with polymerization temperature but decreases drastically near the melting point of the hexoxecane crystal. In order to clarify the specificity of the solid-state polymerization, the crystal structure of hexoxecane was first analyzed; hexoxecane forms a trigonal crystal with cell dimensions of a = b = 7.917 Å, c = 11.345 Å, space group R3-C3i2, three molecules of 3 symmetry per unit cell. The polyoxymethylene as polymerized from a single crystal of hexoxecane is highly crystalline and the crystallites are definitely oriented with respect to the original crystal. There are three kinds of oriented trigonal polyoxymethylene: i.e., with the polymer chains oriented along the 〈100〉, 〈001〉, and 〈210〉 axes of the hexoxecane crystal. The relative yields of these crystallites depend upon the polymerization temperature. In addition to the ordinary trigonal polyoxymethylene, oriented orthorhombic polyoxymethylene was also found in the case of polymerization during treatment with x-rays.
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  • 191
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 393-395 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 192
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 397-398 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
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  • 193
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 587-593 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Internal motions in an alternating copolymer of ethylene and tetrafluoroethylene were investigated by dynamic mechanical and dielectric measurements and by nuclear magnetic resonance. At 1 Hz the α, β, and γ relaxations were observed at 110, -25, and -120°C in a quenched sample. The activation energy was 76 kcal/mole for the α relaxation and 10.6 kcal/mole for the γ relaxation. These relaxations are attributed to the motion of long and short segments in the amorphous regions, respectively. The β relaxation, which was observed only in the dynamic mechanical experiments, appears to occur in the crystalline regions. The copolymer is isomeric with poly(vinylidene fluoride), but it has a higher melting point and a much lower dielectric loss.
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  • 194
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 595-599 
    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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  • 195
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 601-602 
    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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  • 196
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 621-634 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The role of nonstaggered conformations in polymethylenes and in vinyl polymers is discussed in some detail. In incorporating such conformations into rotational isomeric state treatments, it is essential to so choose rotational states as to assure equitable sampling of configuration space. Tacit identification of rotational states with minima in the conformation energy surface, a common practice at present, may lead to serious errors. The significance and limitations of conformational energy calculations are discussed. It is pointed out that the alleged discrepancy between theory and experiments on the spatial configurations of isotactic polymers of α-olefins in general and of polypropylene in particular is unsupported by valid experiments on polymers of established stereochemical constitution.
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  • 197
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 603-619 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Raman spectral changes resulting from the solid-state 1,4-addition polymerization of conjugated diacetylenes are reported. The monomers show an intense C≡C stretching frequency near 2260 cm-1, where as the polymers showed two strong bands, a C≡C vibration near 2100 cm-1 and a C=C vibration near 1500 cm-1. The presence of both double and triple bonds in the polymers suggests the backbone structure (=C—C≡C—C=)n. The alternate mesomeric structure (—C=C=C=C—)n can be eliminated as a possibility by the presence of the strong C≡C vibration in the polymer. Sequential Raman spectra obtained during radiation-induced polymerization revealed intermediate spectral states between the initial monomer and final polymer. Intermediate-state vibrations first increase and then decrease in intensity as polymerization proceeds. However, the observed vibtrational frequencies of intermediate states were not dependent upon the extent of polymerization. Whether polymerization occurred thermally or as a result of radiation did not appear to influence the spectrum of the final polymer, but the observed number of intermediate states differed. Polymerization mechanisms, required molecular motions, and resulting structural changes are discussed.
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  • 198
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 825-840 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The most stable conformations of typical isotactic helical polymers, polypropylene (PP), poly-4-methyl-1-pentene (P4MP), poly-3-methyl-1-butene (P3MB), polyacetaldehyde (PAA), and poly(methyl methacrylate) (PMMA), were analyzed without fixing the fiber identity period by taking into account the intramolecular potential energy due to the internal rotation barriers, and van der Waals and electrostatic interactions. According to the results of the calculations, the number of chemical units per turn N in the stable conformations is 2.91 for PP (value determined by x-ray diffraction: 3.0), 3.52 for P4MP (3.5), 4.17 for P3MB (4.0), and 3.94 for PAA (4.0). This indicates that the molecular conformations of these four polymers are governed primarily by intramolecular interactions, i.e., steric hindrance of side chains, and are additionally modified by the intermolecular interactions in the crystal. For PMMA, the lowest minimum in the potential map corresponds to N = 12, but the energy difference between the minima of N = 12 and N = 5 (corresponding to the actual one) is only 3 kcal/mole of monomer unit. The (5/1) helix of PMMA may be reasonably interpreted in terms of the intermolecular interactions mainly due to the polar and bulky side groups. The intermolecular interaction energy of isotactic PAA in the crystal lattice is also calculated and discussed.
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  • 199
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 861-873 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Heat capacities of molten polyethylene, polypropylene, poly-1-butene, polystyrene, and poly(methyl methacrylate) were measured over a wide range of temperature by using a differential scanning calorimeter. The upper limit of temperature was established for each polymer at about 10°K below the beginning of thermal decomposition. For poly-1-butene and poly(methyl methacrylate) the solid-state heat capacity was also measured starting from room temperature. Several samples of each polymer were used so that average values of heat capacities could be established (reported in 10°K intervals). The data revealed for all polymers a nearly linear increase of heat capacity with increasing temperature over the whole temperature range investigated.
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  • 200
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    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 909-917 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Over the last decade, empirical evidence has indicated that the effective surface energy γ associated with the fracture of noncrystalline is a linear function of the reciprocal of the viscosity-average molecular weight: \documentclass{article}\pagestyle{empty}\begin{document}$ \gamma = \gamma _\infty - b\bar M_v ^{ - 1} $\end{document}. For poly(methyl methacrylate), data of J. P. Berry, G. C. Berry and Fox show that gamma; ∼ 0 at about the same value of M̄v that corresponds to the polymer chain-entanglement length. From this fact, we have developed an entanglement network model for fracture, that bears a resemblance to F. Bueche's entanglement model for the melt viscosity of bulk polymers. Our model allows for the expression of the previously empirical constants, γ∞ and b, in terms of molecular parameters: \documentclass{article}\pagestyle{empty}\begin{document}$ {{\gamma _\infty = \gamma _{\rm s} A_{\rm s} Z_{\rm c} \rho _{\rm c} N_A } \mathord{\left/ {\vphantom {{\gamma _\infty = \gamma _{\rm s} A_{\rm s} Z_{\rm c} \rho _{\rm c} N_A } {\bar M_{\rm s} }}} \right. \kern-\nulldelimiterspace} {\bar M_{\rm s} }} $\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$ b = 2({{\bar M_v } \mathord{\left/ {\vphantom {{\bar M_v } {\bar M_n }}} \right. \kern-\nulldelimiterspace} {\bar M_n }})\gamma _\infty M_{\rm f} $\end{document} where M̄n and M̄f are the number-average molecular weights of the polymer and of the free chain ends, M̄v is the viscosity-average molecular weight, γs is the average fracture-energy per entanglement in the craze volume, As is the average cross-sectional area of the polymer chain, Zc and ρc are the thickness and density of crazed material on the fracture surface, respectively; M̄s is the average strand molecular weight between entanglements, and NA is AvogadrO's number.
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