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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. S30 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 1673-1677 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The parabolic law, according to the equation , of the elasticity in the relaxation phenomena of molten polymers can be deduced from the consideration of the feature that the experimental stress relaxation curves show log-log plots which are often linear in a broad field. A general analysis, only on the basis of the viscoelastic equation permits calculation of relaxation functions, which are suggested as possible means of polymer characterization.
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  • 3
    Electronic Resource
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 1691-1695 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Comparisons were made of changes in molecular weight and in tensile strength of regenerated cellulose after exposure to 40% KOH at 90°C., for varying lengths of time. In the absence of air, both parameters decreased in a fairly consistent manner. In the presence of air, an initial steeper drop was followed by an irregular up-and-down pattern. The theory is advanced that the increase in tensile strength was caused by increased crystallinity.
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  • 4
    Electronic Resource
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 2053-2066 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Experimental results for the sorption of liquid ethanol by a variety of modified wools are described. Even slight changes in the chemical and physical structure of wool produced large changes in ethanol sorption rate. Blocking of amino groups decreased the sorption rate due to removal of primary sorption sites, but, surprisingly, carboxyl group modification greatly increased the rate. Modification of disulfide crosslinks increased the rate, while in most cases surface modification decreased it, which is contrary to expectation if a surface barrier to diffusion of penetrants is assumed. Theories are advanced for the observed changes in sorption properties and for the small changes found when water if used as sorbate. Saturation sorption values showed only slight changes from that for untreated wool. The largest increases resulted from disulfide bond modification, which is explained as due to lower resistance of the treated wool to swelling forces, allowing greater swelling and sorption.
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  • 5
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: An improved cell which permits the measurement of permeabilities of membranes to gases over a wide range of temperatures and gas pressures is described. The measurements are made by the variable volume method, under constant pressure differential across the membrane. The cell lends itself particularly well to routine tests, because it does not require calibration or the use of vacuum techniques. The performance of the cell is discussed, and typical experimental results are presented. A modified permeability cell of the same type for high-pressure studies is also described. Measurements with this apparatus show that the rate of gas permeation obeys, in some cases, a single from of Fick's law, even under pressure differentials across the membrane as high as 800 psi (54 atm.). The paper also compares permeability data obtained by the variable volume and the variable pressure methods. The permeability of 0.002 in.-thick Alathon 15 polyethylene to oxygen and nitrogen was determined between 0 and 50°C. by the two methods, using the same sample of membrane in situ, and the measurements were found to agree within experimental error. Permeabilites of 0.010 in.-thick samples of Alathon 15 polyethylene to nitrogen, oxygen, helium, and carbon dioxide obtained in the same temperature range by the variable volume method were 15-30% higher than the corresponding data determined by the variable pressure method. This discrepancy could be due to the fact that the variable pressure measurements with the thicker membrances may not have been made under true steady-state conditions, although permeabilities were determined from apparently linear sections of permeated gas pressure vs. time curves. A critical re-examination of the methods used to determine permeability constants is suggested.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 2105-2120 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: It was concluded in the preceding paper that there was a significant difference between the indices m and n in the expression A = βWm and F = αWn by which the contact area A and the friction F were found to be related to the load W when nylon 610 slid on glass. A discussion of published adhesion theories of the friction of elastic bodies shows that the difference n - m is too small to be attributed to roughness of the nylon surface. It is concluded that under the contact pressures used the nylon surface was effectively smooth and that the friction of a unit area of “true” (i.e., molecular) contact between nylon and glass increased with pressure P as about P1/4. A theoretical treatment is given of the dependence of friction on load for a rough-surfaced elastic body which covers the load range in which the surface asperities become completely flattened. It is shown that from measurements of the elastic properties of the body and feasible measurements of its surface texture one can estimate the load at which the dependence of friction on load changes from that for a rough to that for a smooth surface. Comparison with a published experiment is satisfactory.
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  • 7
    Electronic Resource
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 2075-2103 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: An apparatus which permits the simultaneous measurement of kinetic friction and contact area between polymer hemispheres and a smooth glass surface has been used to study the dependence of friction and contact area on load, specimen radius, sliding speed, and loading time. Hemispherical nylon 610 specimens of radii 0.12-0.58 cm. have been used with loads of 0.7-200 g. and sliding speeds from 10-7 to 3 × 10-2 cm./sec. All measurements were performed in air at 20°C. and 66% r.h. The contact area was estimated from optical interference fringes (Newton's rings) between the surface of the specimen and that of the glass plate, by means of a theoretical expression, experimentally verified, for the shape into which an elastic hemisphere is deformed when pressed against a rigid plane. The contact area was negligibly affected in size or shape by the presence of the tangential force of friction, in accord with the theory for the contact of elastic spheres. The deformations of the specimens were, within experimental error, completely recoverable but depended on the time of loading. The effects of changes in the four variables, load, radius, speed, and time were found to be essentially independent. Subsidiary experiments showed that both friction and contact area increased by about 10% for each factor-of-10 increase in loading time in the range 5-1000 sec. and that friction increased by a factor of 3 as sliding speed increased from 10-7 to 3 × 10-2 cm./sec. The main series of measurements (at constant sliding speed and loading time) showed that the dependence on load W of both the contact area A and the friction F could well be represented by the expressions: A = βWm and F = αWn (where α and β were constants for a given specimen). The values of m and n were almost independent of specimen radius and their mean values, for 15 specimens, were 0.708 ± 0.006 and 0.781 ± 0.012, respectively. The difference between these values, 0.073 ± 0.013, is statistically highly significant and in the following paper is interpreted as implying that the friction per unit area of true contact between nylon and glass increases with pressure. The dependence of A on the specimen radius R (which is included in β) was found to be as R0.576. The value of this index of R and the value of m are both consistent with a power-law dependence of mean contact pressure on deformation (measured by the ratio of contact to specimen radius) with index 0.82. The values of α for specimens of the same radius showed too much variation for a useful estimate of the dependence of F on R to be obtained.
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  • 8
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: An interesting series of high molecular weight thermoplastic polymers, based on dihydric phenols and epichlorohydrin, have been prepared. The polymers have, in common, a structure which can be represented by the general repeating unit where E is a radical residuum from a dihydric phenol. Certain properties appear characteristic of this class of polymers. All contain some chain branching through the secondary hydroxyl group. They are amorphous, noncrystallizable, transparent, tough, and thermally stable. They show two glassy state transitions, a minor transition at about -70°C. and a major transition at a considerably higher temperature. This family of polymers provides an excellent means for studying structure-property correlations. Data are reported showing the effect of the structure of the dihydric phenol moiety (E) on the major glass transition temperature and on certain barrier properties of a series of these polymers. The polymer prepared from 2,2-bis(4-hydroxyphenyl) propane, bisphenol A, is considered typical of this series; its mechanical and physical properties are described in somewhat more detail and compared with properties of certain commercial polymers.
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  • 9
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 2121-2133 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Powders and compacted preforms of virgin unmelted polytetrafluoroethylene were subjected to ionizing radiation in high vacuum. The specific gravities, melt Visccmities, and mechanical strengths of the irradiated samples after a standard heating cycle in air or at reduced pressures indicate that degradation is more pronounced in the presence of oxygen than in vacuum. The presence of oxygen in the excessively degraded sample was shown by electron spin resonance and pyrolysis experiments. It is suggested that some branched molecules are also formed on heating the irradiated samples resulting in a broadening of the molecular weight distribution. Primary fluorocarbon radicals of the type . disappear rapidly when heated at 75°C. in vacuum while secondary radicals are stable thermally at 200°C. and disappear only slowly at 400°C. Both typea of radicals react rapidly with oxygen and tetrafluoroethylene at 0°C. The reactions which occur in irradiated polytetrafluoroethylene in various atmospheres and at several temperatures are reviewed in light of the information developed during this research.
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  • 10
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The glass transition temperature and gas barrier properties of a number of high molecular weight thermoplastic hydroxyether copolymers have been determined. These copolymers were derived from mixtures of two dihydric phenols and epichlorohydrin. The property data are analyzed in terms of copolymer composition and the random or alternating distribution of monomer units in the polymer chains. In general, the glass transition temperatures of the copolymers were found to be intermediate between the values for the two homopolymers. In one system, good agreement between the experimental data and a simplified equation for the prediction of glass transition temperatures of amorphous, random copolymers was obtained. No differences in the glass transition behavior of random and alternating hydroxyether copolymers could be detected. Gas barrier properties, in general, were found to be intermediate in value between those of corresponding homopolymers. The exceptions are discussed in terms of polymer structure variations.
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  • 11
    Electronic Resource
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 2161-2174 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Chemical changes occurring in thermoset polyesters during exposure to solar and carbon-arc radiant energy were determined quantitatively by a color reaction with a diamine, N,N-dimethyl-p-phenylenediamine, in a methanol-benzene solution. The amount of diamine reacting with a specimen and the color change of the treated specimen, as measured by differential reflectance, varied directly with exposure time. Three commercial polyesters (glass fiber-reinforced) exposed under identical conditions showed widely different degradation rates as measured by the amount of N,N-dimethyl-p-phenylenediamine used per specimen. The relative stability of the three materials was independent of irradiation source. The color of the treated specimen was dependent on exposure time.
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  • 12
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 2183-2197 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A series of gas permeability studies of plastic membranes demonstrated the strong dependence of gas transport on structural aspects of the membrane. Films of cellulose acetate butyrate, silicone rubber, polyethylene, polypropylene, and vinyl chloride, were used in these studies. The effect of elastic and nonelastic stretching, orientation, plasticization, and phase changes were shown to be detectable by gas permeations. Interpretation of the permeation response, as a function of temperature, is compatible with a thermodynamic appraisal of the permeation process.
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  • 13
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 2153-2160 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The esterification of high molecular weight hydroxyether polymers, derived from dihydric phenols and epichlorohydrin, has been studied. The esters of an assortment of monobasic acids, both organic and inorganic, were prepared by reaction of acid halides, anhydrides, esters or free acids with the secondary hydroxyl group in the polymer repeating unit. The effects of the structure of the acid radical and the degree of esterification on polymer properties were determined. In general, esterification resulted in a lowering of the major glass transition temperature of the polymer. This was true at all levels of esterification. Decreased chain symmetry and decreased hydrogen bonding appeared to be the major causes of the observed effect. Permeability of the polymers to oxygen and water vapor was increased by esterification. The increases was found to correlate well with the size and polarity of the acid radical. Some additional properties of the ester derivatives were examined in less detail.
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  • 14
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    Journal of Applied Polymer Science 7 (1963), S. 2175-2182 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A thermodynamic interpretation of the permeation process of gas transport through polymeric membranes is proposed. The mechanism used does not require the usual P = DS relationship. The dependence of gas permeability upon the crystallinity, strain, etc. is presented, and a method for obtaining values for the entropy of crystallization is suggested. Literature data have been correlated by this approach and values for the entropy of crystallization of polyethylene, polyethylene terephthalate, and nylon 610 were derived.
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  • 15
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    Journal of Applied Polymer Science 7 (1963), S. 2211-2216 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The time-temperature superposition principle appears to apply to filled materials, a change in the proportion of filler being equivalent to a shift along the time axis.
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  • 16
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    Journal of Applied Polymer Science 7 (1963), S. 2199-2209 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The kinetics of low-temperature (60-100°C.) thermal degradation of deproteinized and deresinified petroleum ether soluble fraction of natural rubber in two chemically inert solvents, cyclohexane and trans-decalin, have been studied. The changes in Mw, A2, and (r2)1/2 at various stages of degradation have been obtained from the lightscattering data. The rate constants and the energy of activation for chain scission have been calculated from the observed variation in Mu. The scission has been found to be random and the average energy of activation is 25.8 kcal./mole. This low-energy requirement suggests the presence of weak links in the rubber molecule which get ruptured at low temperature.
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  • 17
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: In a continuation of a previously reported investigation into the effect of the catalyst in the cotton cellulose-DMEU reaction, experiments were performed in which the four inorganic salt catalysts originally studied, MgCl2, Mg(NO3)2, ZnCl2, and Zn(NO3)2, were employed at the higher metal ion concentration of 0.1M, and CuCl2 and CdCl2 were employed at 0.03M concentration. Data from infrared absorption spectra of the treated cotton products were in agreement with those obtained at the 0.03M catalyst concentration, again indicating that the catalyst entered into the reaction, forming a coordination complex through the formation of nitrogen-to-metal bonds between the catalyst and the DMEU molecule. Similarly, it was again indicated that reaction with DMEU takes place preferentially at the primary alcohol group of the anhydroglucose unit. Analyses of IR data indicated a higher degree of crosslinking, and thus fewer terminal O—H or N—H groups at the 0.03M catalyst than at the 0.1M catalyst concentration. Further evidence of complex formation was obtained from infrared spectra of the product of the CdCl2-DMEU reaction carried out in the absence of cellulose. Supplemental physical data obtained on products of reactions catalyzed with CdCl2 and CuCl2 at the 0.03M level, when compared with those obtained on products catalyzed with MgCl2 and ZnCl2, supported the earlier hypothesis that chlorine damage during heating was dependent upon the ability of the metallic complex to act as a free-radical trap. Additional support for the free-radical mechanism was obtained when treated cloth subjected to chlorination and exposed to ultraviolet radiation suffered the same discoloring and degradative effect as cloth chlorinated and subsequently scorched according to the usual AATCC method. Reaction rates of the cellulose-DMEU reaction at 45, 55, and 65°C. with each of the four catalysts at the 0.03M concentration were determined by following changes both in nitrogen and formaldehyde content as well as in crease recovery properties. The reaction was found to be pseudo first order when followed to 2/3 completion, and the catalysts, when ranked according to greatest to least effect upon the reaction rates, followed the order: Zn(NO3)2 〉 ZnCl2 〉 MgCl2 = Mg(NO3)2. Enthalpies, entropies, and free energies of activation have confirmed the earlier hypothesis that the metal ion enters into the reaction, forming a transition state complex.
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  • 18
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    Journal of Applied Polymer Science 7 (1963), S. 1117-1132 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Stretched films from partly unsaturated natural rubber hydrochloride develop cracks and fracture in ozonized oxygen. Cracking occurs only above a minimum stress level of about 70 kg./cm.2. Ozone sensitivity increases exponentially with stress, but goes through a maximum near the yield point of the thermoplastic films. Contrary to rubbers, these high-modulus materials do not undergo overall stress relaxation prior to fracturing induced by ozone. The rate of surface ozonization of an unstretched film is estimated gravimetrically and volumetrically; it is found to be similar to that of rubber surfaces. Physical and chemical changes of the ozonized surface are reported. Results are briefly compared with ozone attack on other (nonrubber) materials.
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  • 19
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The oxidative curing and oxidative degradation of cured furfuryl alcohol polycondensates was examined, with infrared spectroscopy, by following the functional group changes occurring in the solid phase of the resin. It has been found that the oxidative degradation of nitrogen-cured resins initially proceeds through the oxidation of methylene linkages to bifuryl ketonic species activated by adjacent furan rings. The second stage of oxidation is the scission of the bifuryl ketonic chain positions to produce substituted furoic acids. The process is postulated to proceed in a manner analogous to that observed in phenolic resin systems. The curing of furfuryl alcohol resin in air is shown to be a multistep process in which the initial oxidation of methylol groups to carboxylic acids is competitive with further polymerization through methylol condensation at adjacent furan ring alpha hydrogen positions. In addition, the oxidation of already formed methylene linkages to the bifuryl ketones is a competitive process removing methylene linkages after they are produced during further condensation (curing reactions). These routes of degradation are in good agreement with observed oxidations of furfuryl alcohol resins under more drastic conditions and offer a reasonable mechanism for resin degradation consistent with observations in analogous polymer systems.
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  • 20
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    Journal of Applied Polymer Science 7 (1963), S. 2269-2292 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Fracture and microtome sections of polyblends, prepared from varying proportions of poly(vinyl chloride) and an elastomer (with and without talc fillers) and with the use of different conditions of mixing, were examined with the electron microscope. In general, the structures observed in cut and in fracture sections were very similar when taken from the same polymer at the same reference planes with respect to direction of process-induced orientation. Optimal tensile behavior seems to occur when the degree of mixing establishes a structure resembling a fibrous interweaving of continuous domains. Undermixing or overmixing seems to establish more random dispersions of more or less large and discrete particles of rubber in a continuous poly(vinyl chloride) phase. Introduction of fillers changes the microstructure of the fracture patterns. Particularly in polymers containing talc fillers, the influence of prior strain history on microstructure is very evident. Thirty-eight figures are shown to demonstrate how differences in composition, mixing process, and strain history can alter the microstructure produced by fracture or cutting of the plastic.
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  • 21
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    Journal of Applied Polymer Science 7 (1963), S. S27 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 22
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    Journal of Applied Polymer Science 7 (1963), S. 2307-2318 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The irradiation of polyethylene causes a number of molecular rearrangements in the chemical structure of polyethylene. In addition to the significant changes in the type and distribution of unsaturated groups, an infrared comparison of the radiation induced chemical changes that occur in air and in a vacuum showed that the presence of oxygen has a marked influence on the structural rearrangements that occur on irradiation. The infrared spectra of irradiated single crystals prepared by two different means indicated the location of vinyl groups in the crystals and their protection from radiation by aromatic structures. From these data, a number of reaction mechanisms are postulated which can contribute to our understanding of irradiation effects on polyethylene.
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  • 23
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    Journal of Applied Polymer Science 7 (1963), S. 2319-2322 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A simple analytical technique has been developed to determine the amount of carboxyl groups present in degraded polyethylene film. This procedure is based upon the relative reactivities of the various carbonyl groups present, in oxidized polyethylene film, to sulfur tetrafluoride gas. The quantity of the carboxyl groups in the film is then measured as a function of the absorption at 5.45 μ.
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  • 24
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    Journal of Applied Polymer Science 7 (1963), S. S15 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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    Notes: The time taken to break under fixed load has been measured for three SBR-filler systems. Two SBR-HAF black systems were used, one vulcanized with sulfur and the other with dicumyl peroxide; the third system was an SBR-silica formulation. Measurements at several temperatures between 30 and 100°C. allowed the computation of an activation energy for the breaking process: 45 kcal./mole for all three systems. By measuring the tensile strength of the filled stock in air and vacuum at various temperatures, it was shown that the presence of oxygen seriously decreases the strength of the filled stock at high temperatures, an effect not present in the gum stock or in silicasilicone stocks.
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    Journal of Applied Polymer Science 7 (1963), S. S45 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Journal of Applied Polymer Science 7 (1963), S. S19 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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    Journal of Applied Polymer Science 7 (1963), S. S21 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Journal of Applied Polymer Science 7 (1963), S. S51 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Journal of Applied Polymer Science 7 (1963), S. 1257-1263 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Using a relationship found to be applicable for natural rubber networks in establishing contributions of chemical crosslinking, entanglements, and networks defects to physical crosslinking, a physical versus chemical crosslinking “calibration” is developed for polybutadiene prepared by organolithium initiation. This calibration is then used to determine chemical crosslink yields for sulfur-sulfenamide, thiuram, and peroxide vulcanization. Crosslink yields for polybutadiene in the sulfur-sulfenamide and thiuram curing systems are shown to be similar to those of natural rubber. In peroxide vulcanization the crosslink yield is in excess of unity for polybutadiene. Evidence is presented which indicates that this is due to a polymerization type reaction involving vinyl groups resulting from 1,2-addition during polymerization.
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  • 31
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    Keywords: Chemistry ; Polymer and Materials Science
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    Notes: The mechanism of precipitation of acrylonitrile polymers was investigated using different nonsolvents. The effect of the dielectric constant and the polarity of individual bonds in the molecule of precipitant is discussed briefly. A methyl methacrylate-acrylonitrile copolymer was successfully fractionated from dimethylformamide solution, using a two-stage fractionation technique, and a mixture of (2 parts n-hexane + 1 part ether) as a precipitant. The molecular weight distributions of primary fractions were skewed to the left and overlapped each other. A large, 100-g. sample of the same copolymer was separated into eight primary fractions, which on refractionation gave a result substantially the same as that obtained by the small scale experiment. An experimental terpolymer of methylvinylpyridine-vinyl acetate-acrylonitrile, prepared by suspension polymerization, was carefully fractionated by the same method. The polymer was shown to have a double-peak molecular weight distribution in agreement with the earlier suggestion that acrylonitrile in aqueous suspension polymerizes by two simultaneous mechanisms: (1) homogeneous polymerization of single radicals in solution, and (2) heterogeneous growth of radicals present in stable suspended polymer particles. The above conclusion was further supported by methylvinylpyridine analysis on secondary fractions. It was found that the low molecular weight fractions contained appreciably more of the water-soluble monomer (M.V.P.), than the high molecular weight fractions.
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    Journal of Applied Polymer Science 7 (1963), S. 1265-1271 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: An electrochemical mechanism is sought for to explain the sudden transient change of potential across a nerve membrane during neural conduction. Ion-permselective membranes change the sign of their permselectivity if the charge of their fixed ions is overcompensated for by highly charged counterions which become strongly bound to these fixed sites by electrostatic forces. Imagine a membrane with its sign thus reversed beyond a given borderline: cations could traverse on one side in the vicinity of this line and anions on the other, while no ions would traverse pure membrane faces themselves. Thus concentrations would be equalized at the borderline by passive diffusion, while the sign of membrane potential would change from one side to the other of the border. A mechanism for automatic propagation of the border along the membrane is suggested. Sign reversal of membranes can also be caused by covalent bonding of oppositely charged groups to a charged membrane site, for instance by esterification of a carboxyl group or of a phosphoric acid group of a lipoproteid nerve membrane with the amino alcohol choline. Hydrolysis of such an ester would cause the sign of the membrane to revert to its original direction. Such acetic sites and choline abound on nerve membranes, together with enzymes, which are known to split and synthesize choline esters. Their electrochemical function in neutral conduction might well be this changing of sign of membrane permselectivity.
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    Journal of Applied Polymer Science 7 (1963), S. 1281-1289 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A theory is presented of the way in which the melting of a polymer is manifested in a differential temperature analysis thermogram. An analytical method based on this theory allows a precise determination of both the melting point and the crystalline weight fraction as a function of temperature. Experimental results for linear polyethylene and crystalline polypropylene confirm the theory.
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    Journal of Applied Polymer Science 7 (1963), S. 1307-1315 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Infrared and near-infrared spectra of 3-methylbutene-1 were observed for the vapor phase at room temperature. Also, Raman displacements and depolarization factors of 3-methylbutene-1 in methanol and carbon tetrachloride were obtained at the same temperature. Tentative assignments of the observed Raman and infrared bands were made, and a classification of bands on the basis of group frequencies is given.
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    Journal of Applied Polymer Science 7 (1963), S. 1273-1279 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A recording apparatus for measuring longitudinal creep was developed to study viscoelastic properties of polymeric films. The heart of the apparatus is a photoelectric transducer that converts specimen extension and contraction into a voltage which is then applied to a millivolt recorder through a d.c. low-drift amplifier. As used in this apparatus, the phototube detects the variable by having its photocathode surface shadowed by a movable mask. Supplementing the recording part of the apparatus is a mechanism for controlling specimen temperature. A polymer of plasticized polyvinyl chloride was studied, to demonstrate the applicability of the apparatus. The results obtained compared favorably with the method of visually observing the displacement with a cathetometer.
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    Journal of Applied Polymer Science 7 (1963), S. 1291-1306 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The temperature dependence at constant frequency of the viscous component E2(1/T) of the dynamic modulus has been determined for a homologous series of butadiene-acrylonitrile copolymers supported in a matrix of styrene homopolymer. The results, which agree with those reported earlier for a homologous series of butadiene-styrene copolymers, indicate that the transition temperature of a given plastic homopolymer, as measured from dynamic mechanical properties at essentially constant frequency in the range 200-300 cycles/sec., is depressed by the presence of a copolymerized rubbery diluent as the melting point of crystalline polymers is depressed by the presence of noncrystallizing comonomers. In addition, it has been found that the transition temperature is depressed by the presence of monomeric diluents much as the melting point of crystalline polymers is depressed by the presence of monomeric diluents. Two earlier assumptions, that the dynamic properties in the frequency range of interest should be independent of both the molecular weight of the rubbery copolymer and the degree of dispersion of the copolymer in the thermoplastic matrix, have been subjected to experimental scrutiny. The assumption regarding the dependence on molecular weight has been substantiated, at least for DP's in excess of 100. The assumption regarding the dependence on the degree of dispersion has been negated; the area under the E2(1/T) peak was found to be considerably greater for a coarse dispersion than for a fine one.
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    Journal of Applied Polymer Science 7 (1963), S. 1317-1323 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: A convenient technique is presented for determination of triboelectric characteristics of a film sample relative to a group of reference surfaces and to other film samples, with the use of inexpensive, easily assembled equipment. It consists of pressing a number of reference surfaces into contact with a test film, determination of the sign and intensities of the charges generated, by spraying with an indicating powder, and estimation of tribo-electric position of the test sample by the distribution of positive and negative charges generated. With this technique, relative triboelectric characteristics were determined for films of various polymers. The measurements give some insight into the relation between polymer structure and triboelectric characteristics.
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    Journal of Applied Polymer Science 7 (1963), S. 1341-1347 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: By use of a reference value of modulus equal to 109 dynes/cm.2 and a reference value of time equal to 10 sec., characteristic viscoelastic parameters are defined from stress relaxation master curves and from modulus-temperature curves. Values of these parameters are tabulated for several linear amorphous polymers and slightly crosslinked amorphous polymers.
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    Journal of Applied Polymer Science 7 (1963), S. 2003-2023 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: At temperatures far below the heat distortion point, the dissipation factor (and therefore power factor) of epoxy resins is comparably low - in the order of 0.001-0.01. Internally flexibilized, polyester-modified resins may have higher loss tangents, in the order of 0.01-0.10, even at room temperature. At temperatures far above the heat distortion point, anhydride curing agents give lower dissipation factors than do amines or acids. With anhydride cures, the higher molecular weight resins investigated cure faster than the lower molecular weight resins, give lower elevated temperature power factors and loss tangents, and are tougher. With any hardener-epoxy resin system, the optimum elevated temperature power factor, weight loss on aging and heat distortion point will probably depend on a close examination of the optimum hardener/resin ratio.With certain anhydride-cured low molecular weight epoxy resin systems, an increased rate of cure and lower elevated temperature power factor may be obtained by use of a small amount of higher molecular weight (polyhydroxy) epoxy resin. Attempts to compare the effect on power factor of changing the hydroxyl groups to less mobile dipoles by acetylation were unsuccessful, since the resulting acetoxy groups changed the cure mechanisms. However studies with resins of different molecular weights indicated that the effect of hydroxyl content on elevated temperature power factor is subordinate to other effects such as the rigidity of the cured resin system, rate of cure and ionic impurities. Acetylation of hydroxyl-containing epoxy resins may inhibit cure with some curing agents, due to side reactions of the resulting acetoxy group with specific hardeners.
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    Journal of Applied Polymer Science 27 (1982), S. 11-19 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Approximate analytic results for two problems involving the inflation of rubber inner tubes and tires are summarized with a view to prompting a comparison of the theory with experimental results. The problems considered are the uniform inflation by internal pressure of a toroidal rubber inner tube or tire which is a perfect torus either in the deformed or undeformed state. The inner tubes or tires are assumed to be free to inflate, that is, they are assumed not to be constrained, for example by a wheel.
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    Journal of Applied Polymer Science 27 (1982), S. 53-62 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Temperature dependencies of viscoelastic functions of the three-component models of composite materials in the transition state temperature range of polymer binder have been studied. On the basis of theoretical calculations for the models, a conclusion has been made about the conditions for shift of the relaxation maxima along the temperature axis. Also conditions for their resolubility on tan δ curves were determined for materials such as filled polymers as well as anisotropic laminated and reinforced plastics with deformation of the components in series. These effects are due to the change in properties of the boundary layer of the polymer. They are entirely dependent on the concentration ratio between the boundary layer and the bulk of the binder polymer and on the difference in their glass temperatures Tg. Concentration of the high-modulus filler affects Tg of the composition. This is due to the change in the ratio of concentrations of the polymer in the boundary layer and in the bulk. With parallel deformation of the components of the three-component model, resolubility and shift of the relaxation maxima depend not only on the above factors, but also on the reinforcing filler concentration.
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    Journal of Applied Polymer Science 27 (1982), S. 79-87 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: The water and salt transport properties of untreated and heat-treated poly(vinyl alcohol) (PVA) membranes were investigated. Water and salt permeabilities decreased abruptly as a result of heat treatment. The effect of heat treatment on the water and salt transport in PVA is expressed mainly by changes in the activation energies of the corresponding permeability coefficients. Due to the fact that the decrease in the salt permeability with heat treatment was considerably greater than the decrease in the water permeability, a pronounced improvement in the salt rejection of PVA membranes was found as a result of heat treatment.
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    Journal of Applied Polymer Science 27 (1982), S. 113-120 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Poly(vinyl acetate) (PVAc) of M̄w 750,000 M̄w/Mn 3.85 and B̄n (the number of long branches per molecule) 2.2 was subjected to chain scission by mechanical (high-speed stirring) as well as chemical (saponification and reacetylation) methods to investigate the effect of shear on the branching distribution. The extent of long branching was measured by gel permeation chromatography on-line with low-angle laser light scattering photometry. It was concluded that (i) the branches through the acetate group are long and are ruptured preferentially on shearing, (ii) the branches through the α- and β-carbons are not broken on shearing, (iii) the extent of long branching through the acetate group is about 67% of total branching, and (iv) the poly(vinyl alcohol) derived from branched PVAc contains a smaller but nevertheless significant amount of branching.
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    Journal of Applied Polymer Science 27 (1982), S. 149-159 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Crosslinked polymers based on the condensation of furfural with N-vinylcarbazole and poly(N-vinylcarbazole) were prepared. The effect of variation of furfural concentration on the condensation of furfural with N-vinylcarbazole and its polymer was studied. The polymers were chemically modified into phosphonic acid cation exchange resins. The effects of variation of AlCl3, PCl3, and furfural amounts, reaction time, and rephosphorylation on the synthesis and capacities of cation exchange resins were also studied.
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    Journal of Applied Polymer Science 27 (1982), S. 211-223 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The degradation mechanism of styrene-polyester copolymer was studied by various experimental techniques such as TGA, DTA, IR spectroscopy, pyrolysis gas chromatography, and GCMS (gas chromatography-mass spectrometry). It is concluded that, mainly, there are two first-order degradation reactions during thermal degradation in the presence of air. The first step involves the scission of crosslinks/weak links with liberation of free linear chains. The second degradation step involves random scission of the free linear chains into smaller fragments. The various fragments were identified by pyrolysis gas chromatography and by GCMS. In oxygen atmosphere, the polymer was found to obey first-order kinetics with a single rate constant. Apparently, due to presence of oxygen species at the degrading surface, the two rate constants obtained during thermal degradation reaction are altered in such a fashion as to give a single rate constant.
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    Journal of Applied Polymer Science 27 (1982), S. 247-257 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Permeant degradation affects the brittleness, flexural fatigue, and ultimate tensile properties of polyester fibers more drastically than topochemical degradation. Topochemical degradation was obtained by hydrolysis with aqueous NaOH and permeant degradation by aminolysis with aqueous ethylamine. Treatment with aqueous sodium hydroxide appears to leave the polyester fiber surfaces more resistant to abrasion damage.
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    Journal of Applied Polymer Science 27 (1982), S. 1177-1190 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A polymer with high aromaticity and/or cyclic ring structures chain backbone usually has high heat, thermal, and flame resistance. Two diglycidyl ethers of bisphenols were prepared from 4,4′ isopropylidenediphenol (DGEBA) and 9,9-bis(4-hydroxyphenyl) fluorene (DGEBF) for evaluation. Four boroxines - trimethoxyboroxine (TMB), triethoxyboroxine (TEB), triisopropoxyboroxine (TIPB) and triphenoxyboroxine (TPB) - were used as the curing agents. DGEBA and DGEBF cured with various boroxines indicate that the trend for their respective glass transition temperature (Tg's), degradation temperatures (Td's), and gel fractions are TMB-cured epoxy ≈ TEB-cured epoxy 〈 TIPB cured epoxy 〈 TPB cured epoxy. The DGEBF system usually has a higher Tg, Td, gel fraction, oxygen index (OI), and char yield than the related DGEBA system. DGEBF/DGEBA (80/20 mol ratio) shows a synergistic effect in regard to char formation. This effect exists not only in the copolymer system but also in blended homopolymers of the separately cured resins. A modified mechanism for the polymerization of phenyl glycidyl ether (PGE) with TMB has been proposed.
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    Journal of Applied Polymer Science 27 (1982), S. 1217-1231 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Three simplified models of polycondensation reactors are considered in which the condensation product is continuously removed by application of vacuum. Reversible polycondensation reactions of monomers violating the equal reactivity hypothesis have been simulated in these reactors. The effect of various rate and reactor design variables on the molecular weight distribution (MWD) and its moments is studed. It is observed that when the reverse reactions are rapid, the results are fairly sensitive to the level of vacuum applied and to the mass transfer resistance; whereas when the forward reactions predominate, results lie very close to earlier plots for the corresponding irreversible polymerizations. These reactor variables then have relatively small influence on the MWD. Splitting of the MWD curves for odd and even values on n is observed under certain conditions, the effects being more pronounced in the presence of mass transfer than in its absence.
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    Journal of Applied Polymer Science 27 (1982), S. 1259-1268 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The effect of the specific surface area of silica gels on the radiation-induced polymerization of styrene adsorbed on silica gel was studied by ESR. The same radicals were generated on the silica gels regardless of the specific surface area, but the stability of the radicals at room temperature depended on the specific surface area. This means that the decay of the radicals proceeded mainly on the surface of the silica gel. Almost all the radicals generated by irradiation were initially in the bulk of the silica gel and migrated from the interior to the surface of the gel. When styrene monomer was adsorbed on the surface of the silica gel, the silica gel radicals interacted with the monomer and initiated polymerization and then generated polymer. The rate of migration of the silica gel radical was rather fast in the case of silica gel with a large specific surface area. Thus, the polymerization behavior of styrene adsorbed on silica gel greatly depended on the specific surface area of the gel.
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    Journal of Applied Polymer Science 27 (1982), S. 1313-1319 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Kinetics of grafting of poly(butyl acrylate) onto gelatin was studied with H2O2 - ascorbic acid redox systm. Percent grafting, grafting efficiency, Rg, and Rh were determined as a function of time, temperature, initiator, monomer, and backbone concentration. It was found that Rg depends on first power of monomer concentration and 0.5 power to the initiator concentrations. A detailed kinetic scheme is proposed to explain these results.
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    Journal of Applied Polymer Science 27 (1982), S. 259-269 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Phosphate coupling agents, i.e., alkyl dihydrogenphosphates containing functional groups such as olefinic, chloro, methacryloxy, and mercapto, were synthesized and allowed to react with calcium carbonate filler suspended in an aqueous medium. The modification provided the filler with good dispersibility in mineral oil. Physical properties of the vulcanized rubbers loaded with the modified fillers were found to be influenced by the functional group introduced. For example, in peroxidecured ethylene-propylene-diene rubber (EPDM), the methacryloxy group was most effective, and the mercapto group significantly enhanced the physical properties of sulfur-cured styrene-butadiene rubber (SBR), while a saturated aliphatic phosphate was ineffective in both curing systems. Deposition of the coupling agent as calcium salt onto calcium carbonate surface was observed by scanning electron micrography. The novel approach for the surface modification of calcium carbonate filler is descussed in relation to the reinforcing effects on rubbery materials.
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  • 52
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    Journal of Applied Polymer Science 27 (1982), S. 319-326 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The room temperature gamma irradiation degradation of the lithographic polymers, poly(methylmethacrylate) (PMMA), poly(methyl-α-chloroacrylate) (PMCA), poly(methyl-α-fluoroacrylate) (PMFA), and poly(methylacrylonitrile) (PMCN), have been studied by electron spin resonance and electron nuclear double resonance (ENDOR) to assess their molecular degradation processes of relevance to electron beam lithography. Two classes of radicals are found, chain radicals and chain scission radicals. PMMA and PMCA mainly form chain scission radicals consistent with degradation while for PMCN the resolution is poorer, and this is only probable. PMFA forms mainly chain radicals consistent with predominant crosslinking. The total radical yield is greatest in PMCA and PMCN. ENDOR is used to assess the compactness of the radiation degradation region for PMMA and PMCA and hence the potential resolution of the resist; this appears to be about the same for these methacrylate polymers.
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  • 53
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    Journal of Applied Polymer Science 27 (1982), S. 363-379 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The evolution of the latex particle diameter distribution during batch emulsion polymerization is investigated, with emphasis on changes in the breadth of the size distribution. A model utilizing a surface area-dependent volumetric growth rate of a single particle results in a time-invariant standard deviation of the size distribution during periods of particle growth only. This behavior is reconciled with some experimental observations by considering the occurrence of particle nucleation during some part of the growth interval. Conclusions based on the results of the model suggest that higher inhibitor and low emulsifier concentrations favor narrow particle size distributions.
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    Journal of Applied Polymer Science 27 (1982), S. 425-437 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Epoxy-modified polyolefins have been prepared by the radical grafting of glycidyl methacrylate to polymer melts. The reactions of these materials with amines and carboxylic acids were investigated. The modified polymers undergo typical epoxide reactions.
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  • 55
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    Journal of Applied Polymer Science 27 (1982), S. 471-487 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A comprehensive mathematical model for a continuous transesterification process has been built so as to enable prediction of the influence of different process and operational variables on productivity and by-product formation. The influence of temperatures and temperature profiles, of residence time and residence time distribution, and also of the number of reactors in series has been investigated. The modeling has been done as close to the industrial practice as possible. Important pragmatic implications from the point of view of operation of continuous transesterification are highlighted.
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  • 56
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    Notes: Photochemically induced grafting (1) and graft polymerization (2) from N,N-dimethylformamide solutions of four acryloxy-substituted aromatic diazenes, chosen as model molecules of acryloxy azo dyes, were investigated kinetically at 25°C onto polypropylene, polycaprolactam, and poly(ethylene terephtalate) films, by polychromatic irradiations. Quantum efficiencies at zero concentration of dyes and lifetimes of excited states for processes (1) and (2) were evaluated from experimental data by Stern-Volmer plots. The surface density of grafted molecules at the end of process (1) was not affected by the concentration of dyes in solution, but varied sensibly with the chemical nature of polymers and dyes. The relevant parameters are discussed on the basis of the proposed mechanism.
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    Journal of Applied Polymer Science 27 (1982), S. 559-568 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Poly(caprolactone) (PCL) was blended with poly(chlorostyrene) (PSCI) and chlorinated polypropylene (PPCl). A single glass transition temperature Tg was found for these mixtures, indicating their miscibility. PCL crystallizes in these blends when the chlorinated polymer content is not too high. Otherwise, Tg becomes higher than the melting point of PCL and the high viscosity of the medium hinders the crystallization. The miscibility of PCL/PPCI blends cannot be due to hydrogen bonding between the α-hydrogens of the chlorinated polymer and the carbonyl group of the polyester since PPCI does not have available a large number of α-hydrogens. It is suggested that a dipoledipole —C=O…Cl—C— interaction is responsible for the observed miscibility phenomenon and that this interaction is probably also responsible for the miscibility between all other polyesterchlorinated polymer mixtures. Finally, it was observed that poly(α-methyl-α-n-propyl-β-propiolactone), poly(α-methyl-α-ethyl-β-propiolactone) and poly(valerolactone) are not miscible with PSCI or PPCl, despite the fact that they are miscible with poly(vinyl chloride).
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    Journal of Applied Polymer Science 27 (1982), S. 1707-1717 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The influence of molecular weight on fatigue and fracture behavior in nylon 66 (N66) and polyacetal (PA) is examined. Fatigue crack propagation (FCP) resistance and apparent fracture toughness (Kcf) in these two semicrystalline polymers increase with increasing molecular weight in a manner consistent with that reported for another semicrystalline polymer (HDPE) as well as for several amorphous polymers. The improved FCP resistance with increasing molecular weight is attributed to the development of a molecular entanglement network that more effectively resists cyclic-load-induced breakdown. A type of discontinous crack growth is identified in PA at 100Hz and in N66 (2.6% H2O) at 50 Hz and compared with that observed in amorphous polymers.
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    Journal of Applied Polymer Science 27 (1982), S. 687-695 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Storage and loss elasticity complex moduli E′ and E″ and temperatures at which the α relaxation takes place are studied with respect to thermal history, deformation speed, and molecular weight distribution of drawn linear polyethylene. Maximum values of E′ and E″ increase with draw ratio of the hot-drawn samples, and the α relaxation temperatures increase by around 10°C when the polyethylene filaments are annealed at 110°C. The activation energy of the process, considered as a single one because the symmetrical shape of the maxima, increases with draw ratio, and this increase is less pronounced when the filaments are annealed. Annealing of the filaments produces a decrease in their E′ values, but this decrease is almost negligible for filaments obtained from polyethylene with a broad molecular weight distribution. The final crystallinity of the filaments drawn at room temperature and subsequently annealed is higher for the filaments obtained at lower drawing speed.
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    Journal of Applied Polymer Science 27 (1982), S. 1795-1807 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Water-leaching experiments of halides from polymers were carried out in batch and continuous systems. The effects of flow rate, temperature, and salt content on the leaching kinetics were investigated. Different thermoplastic polymers were used as the salt carrier, and the release kinetics from them was established. NaCl, NaBr, and NaI were leached out completely from nylons, while NaF could only be partially removed. Release mechanisms involving diffusion, capillary flow, and fracturing were described based upon the leaching kinetics and porosity distribution in the resulting foams.
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  • 61
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    Notes: Cotton fabric was crosslinked with DMDEU by applying the Form D-Process and Form W-Process. The cotton and crosslinked cotton were then treated with caustic soda solution of mercerizing strength. The ability of cotton and crosslinked cottons to dyeing with two reactive dyes, viz. Procion Blue MRB and Procion Red HB was examined. It was found that crosslinking reduces significantly the amenability of cotton to reactive dyes particularly when the Form D-Process was applied. Mercerization enhances dyeability of all substrates, but the enhancement was much greater in the case of noncrosslinked cotton. Based on dyeing and other properties such as tensile strength, elongation at break, and crease recovery, it was shown that crosslinking decreases considerably the affinity of cotton to caustic soda solution. It was further anticipated that different color designs with different patterns and properties can be conferred on a given cotton fabric by making use of local crosslinking and/or mercerizing followed by dyeing.
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  • 62
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    Journal of Applied Polymer Science 27 (1982), S. 913-930 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The investigation of the thermal degradation of the char-formaing phenol-formaldehyde resins is conducted to provide information for the systematic design of high temperature flame-resistant phenolics. Three different processes of curing are used: (1) Formaldehyde or s-trioxane is reacted with m-substituted phenol-formaldehyde oligomers under acidic conditions to give the methylene bridged-novolac resins. (2) Phenol and m-substituted phenols are reacted with CH2O under basic conditions and then heated to give the methylene bridged resol resins. (3) p-Terephthaloyl chloride and m-and p-substituted novolac oligomers are reacted to give cured resins with ester linkages. The evaluation of the effect of various substituents indicates that the oxygen index (OI) increases from about 33 for unsubstituted phenolics to about 75 for meta-halogen substituted phenolics. The evaluation of the effect of various crosslinking agents shows that the OI for CH2O-cured phenolics is 75 as compared to 50 for the trioxane cured phenolics and to 40 for the terephthaloyl chloride cured phenolics. A set of phenolic copolymers with different weight percentage content of halogen substituted phenols are synthesized as novolacs and resols. The results surprisingly indicate no increase of OI for the cured novolac copolymers, whereas the increase is observed for the cured resol copolymers. The activation energy for the thermooxidative degradation of the cured novolacs is about 12-15 kJ/mol lower as compared to that of the curd resols.
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  • 63
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    Journal of Applied Polymer Science 27 (1982), S. 1007-1017 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Gas permeability of poly(γ-methyl L-glutamate) (PMLG) membranes prepared by using dichlorethane, trifluoroacetic acid, and formic acid as solvents was studied. The membranes prepared by casting dichloroethane and trifluoroacetic acid solutions of the polymer, designated as PMLG - DCE and PMLG - TFA, respectively, had α-helical structures according to infrared absorption spectra, while the membranes prepared by allowing the PMLG - TFA membranes to swell in formic acid, designated as PMLG - FA, had mainly a β-sheet structure. The diffusion coefficients of each gas studied for PMLG - DCE, PMLG - TFA, and PMLG - FA decreased in that order, and the apparent activation energies of diffusion increased in that order. The apparent heats of solution for Ne,O2, N2, and CO2 were negative in PMLG - FA. These results were discussed in connection with the molecular conformations of PMLG in the membranes. It is suggested that the diffusion of gases in PMLG - DCE takes place in the side-chain regions between helices, while in PMLG - FA the diffusion occurs across the polymer main chain whose mobility is depressed by the intermolecular hydrogen bonds. The effect of water on oxygen permeability of PMLG - DCE was small; on the contrary that of PMLG - FA was very large. Furthermore, it is assumed that the random-coil conformation partly exists in PMLG - TFA.
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    Journal of Applied Polymer Science 27 (1982), S. 1053-1065 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The crystallization, from molten blends, of polypropylene (PP) and polybutene-1 (PB), two highly crystallizable, polymers, their interaction in the amorphous phase, and the resulting tensile mechanical properties were studied. The crystallization was followed by DSC, showing two separate PP and PB crystallization processes which are affected each by the presence of the other component. The crystallization temperature of PP is significantly affected only in PB rich blends whereas that of PB is affected in the whole composition range. The PP crystalline phase, acting as a nucleating agent, increases the PB crystallization temperature whereas the PP amorphous phase, acting as a high viscosity polymeric diluent, reduces the PB crystallization temperature. The first effect is dominant at low PP content, and the second one becomes increasingly effective with increasing PP content in the blend. The interaction between the two polymers in the amorphous phase was studied by applying dynamic mechanical analysis, in which a single glass transition was observed for the blends and its temperature was found to vary with the blends' composition. Tensile mechanical properties of blends were found to be more sensitive to thermal treatments, such as isothermal crystallization or annealing at elevated temperatures, than single component systems. Such thermal treatments enable better structured blends to be formed, resulting in mechanical properties with no abrupt changes in the whole composition range.
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    Journal of Applied Polymer Science 27 (1982), S. 1091-1093 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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    Journal of Applied Polymer Science 27 (1982), S. 1107-1118 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Polystyrene and its various alkyl and halo derivatives have been studied as homoelectrets and their stabilities under different environmental conditions determined. The stabilities of the homoelectrets prepared from these polymers depended on their volume resistivities, glass transition temperatures, and interactions with electron-acceptor impurities. Excellent stabilities were exhibited by the homoelectrets prepared from polystyrene, poly(vinyltoluene), poly(chlorostyrene), and poly(t-butylstyrene). It is postulated that the charged particles are trapped by the π-orbitals of the phenyl rings present in these polymers and that they are adversely affected by the presence of electron-acceptor compounds that generally from charge-transfer complexes with the phenyl groups.
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  • 67
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    Journal of Applied Polymer Science 27 (1982), S. 1249-1258 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Polymerization of allyl methacrylate (AMA) with wool fabrics using different initiators, namely, potassium persulphate, Fe2+—H2O2, benzoyl peroxide, ceric ammonium nitrate, and vanadium pentanitrate, was investigated. The percent of polymer add-on depends upon the type and concentration of the initiator. Addition of metallic salts such as Fe3+ to the polymerization system enhances polymerization significantly when benzoyl peroxide and potassium persulphate are used independently as initiator. The opposite holds true for ceric ammonium nitrate and vanadium pentanitrate. With Fe2+—H2O2, on the other hand, the enhancement is marginal. Also studied was the incorporation of Li+, Cu++, and Fe3+ at different concentrations in AMA - wool-benzoyl peroxide polymerization systems. Determination of the polymer add-on on the basis of double bond analysis revealed that the remained double bond is governed by the magnitude of the polymer add-on as well as by the type of initiator.
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    Journal of Applied Polymer Science 27 (1982), S. 1277-1291 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Viscosity measurements were carried out as a function of pressure and temperature with solutions of polystyrene in eight (endothermal) θ-solvents at the respective critical composition by means of a Searle-type apparatus. A rolling-ball viscometer was used for the investigation of the pure solvents. In all cases the viscosity coefficient increases in a more or less exponential manner when the pressure is raised. For θ-conditions, the volumes of activation of the solutions exceed that of the pure solvent by typically 10-15%. The exact amount of this extra efffect stemming from the presence of the polymer and its variation with temperature can be qualitatively correlated with the heats of mixing. The ratio of the viscosity of the solution at 1000 and 1 bar, respectively, can be varied for a given solvent power (θ-temperature) by the choice of the solvent from ca. 2 (cyclopentane) to 4 (trans-decalin). Within a given system, the maximum effects that can be realized by a change of the solvent power via the variation of temperature ranges from ca. 3 to 6 (tert-butylacetate).
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    Journal of Applied Polymer Science 27 (1982), S. 1327-1334 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A conversion-temperature phase diagram for thermosetting polymers is analyzed. The curing under different external conditions - isothermal, at a constant heating rate, adiabatic, and in a mold at constant wall temperature - is represented by definite trajectories in the phase diagram. Conditions related to incomplete curing or falsification of kinetic parameters are stated.
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    Journal of Applied Polymer Science 27 (1982), S. 1355-1366 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The formation of volatile aromatic pyrolyzates in poly(vinyl chloride) has been studied by pyrolysis-gas chromatography-mass spectroscopy. Results from isotopic labeling experiments with perdeutero-PVC suggest that the aromatic pyrolyzates can be divided into three general classes with respect to their formation mechanisms: (1) intramolecular - benzene and naphthalene are formed almost exclusively via intramolecular cyclization reactions; (2) mixed intra/intermolecular - styrene and indene can be formed either intramolecularly or via transfer of one hydrogen atom between PVC chains; (3) intermolecular - toluene and methylnaphthalene can be formed via transfer of one or two hydrogen atoms between chains. The isotopic distributions observed in the labeling experiments can be reasonably well explained without involving crosslinking (intermolecular C—C bond formation) reactions.
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  • 71
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    Notes: Rubber-modified polystyrenes were prepared by bulk polymerization with seven different butadiene-styrene copolymers of differing chemical microstructures. The products were structurally characterized through measurement of the swell ratio, percent insolubles, intrinsic viscosity of the soluble fraction, and transmission electron microscope photomicrographs. Increasing initiator concentration or raising polymerization temperature gives lower molecular weight, higher rubber crosslink density, and decreased grafting. Increasing rubber content generally leads to aggregation. Tensile stress-strain curves and Izod impact strengths were measured. High Izod impact strength and increased elongation to break are favored by increasing matrix molecular weight, rubber content, and extent of grafting.
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    Journal of Applied Polymer Science 27 (1982), S. 2513-2526 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The postcondensation of nylon 6 in the solid state was studied. The reactions were carried out on fine powder in a fluidized bed reactor in a stream of dry nitrogen in the temperature range 110-205°C and during 1-24 h. The solid-state polymerization (SSP) did not follow melt kinetics, but was found to be limited by the diffusion of the autocatalyzing acid chain end group. Factors thought to influence SSP were studied, e.g., heat treatment, starting molecular weight, and remelting. Surprisningly, heat treatment had little effect, but the starting molecular weight had a strong effect on the reaction rate. The higher the starting molecular weight, the faster the reaction. This could be explained as a changing concentration distribution of the reactive groups in the solid state on SSP. The kinetics of the SSP had more than one region, and the rate of reaction for conversions of over 30% could be expressed as - dc/dt = k(c/t), where k is a dimensionless constant independent of temperature with a value of 0.28. The integrated form has the form - In(c/co) = k In(t/τ), where co is the acid end-group concentration at the start, t is the reaction time, and τ is the induction time. The value of τ is both dependent on the starting concentration co and the reaction temperature and has an activation energy of 105 kJ/mol.
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    Journal of Applied Polymer Science 27 (1982), S. 2563-2566 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The influence of pH on the emulsifier property (micellar molecular weight) of sodium dodecyl sulfate has been studied in conjunction with the effect of pH on the rate of emulsion polymerization of styrene initiated by potassium persulfate. The rate of polymerization was found to be pH dependent. The micellar weight of sodium dodecyl sulfate has been determined at various pH values. The miceller weight was found to increase with decrease in pH. On the basis of the result, a suggestion was made that the effect of pH on micellar molecular weight can account for the observed behavior of the rate of polymerization.
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    Journal of Applied Polymer Science 27 (1982), S. 2615-2623 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The thermal degradation of PVC was measured under dynamic and static conditions. The UV and IR spectra, as well as the molecular weight distribution of the PVC samples, taken after different time intervals were measured. It was established that during the dynamic PVC degradation, performed in a mixing chamber, two stages with different degradation rates can be distinguished both in extinction and torque vs. time curves. While oxygen does not, dissolved HCl does play an important role in the dynamic degradation: HCl steps into reaction with the formed polyenes and has a catalytic action. The chemical degradation, particularly the crosslinking, produces the changes in the rheological behavior of the material. Results were compared with those obtained under static conditions in argon, air, and HCl atmosphere.
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    Journal of Applied Polymer Science 27 (1982), S. 2663-2674 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A basic study of orientation development in the tubular film extrusion of polypropylene is reported. WAXS and birefringence measurements were carried out on films prepared under conditions of known blowup ratio B, drawdown νL/νO, machine direction tension, and bubble pressure. Pole figures were constructed and biaxial orientation factors determined. The use of an orientation factor triangle diagram was found to be a useful method of representing the variation of orientation with processing conditions. The variation in orientation with processing parameters for polypropylene was found to have similar behavior to that previously found for polyethylene.
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    Journal of Applied Polymer Science 27 (1982), S. 2731-2737 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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    Journal of Applied Polymer Science 27 (1982), S. 2743-2745 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 78
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    Journal of Applied Polymer Science 27 (1982), S. 2783-2789 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: An interpolymer anionic composite membrane for reverse osmosis was prepared from poly(vinyl alcohol) and poly(styrene sulfonic acid). The effects of composition of a casting solution, heat-curing periods, and casting thickness on the reverse osmosis performance of resulted membranes have been examined. A mixture of water and ethyl alcohol (12/7, wt %) was found to be a proper solvent for casting an interpolymer membrane on the supporter. The composite membrane was formed by casting the polymer solution in ultrathin film on a microporous polypropylene supporter, evaporating the solvent, and heat-curing at 120°C for a proper period. the optimum composition of a casting solution was as follows: wt % of poly(vinyl alcohol)/poly(styrene sulfonic acid)/solvent was 3/2/95. The membrane heat-cured at 120°C for 2 h has a good performance for reverse osmosis, viz., water flux of 9.1-28.4 L/m2.h at salt rejection level of 88.1-93.4% under applied pressure of 80 kg/cm2 with 0.5% NaCl aqueous solution. The formation mechanism of a water-insoluble membrane was discussed.
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  • 79
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    Journal of Applied Polymer Science 27 (1982), S. 2751-2760 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The manner in which diethyl phthalate (DEP) is absorbed into nitrocellulose (NC) fibers has been observed microscopically. The movement of pure DEP into dry fibers proceeds by capillary motion up the central canal (lumen) and through microcracks between fibrils. Attack, measured by a large change in birefringence, spreads from these foci, and within the time scale of the experiment there is little interaction with the primary (outer) wall of the fiber. If, however, the lumen and other capillary passages are blocked by water or other liquid, then attack proceeds evenly from the outer wall and a sharp boundary between swollen and unswollen material moves at a uniform speed towards the center of the fiber and appears to be unaffected by the fibrillar structure (Case II swelling). If the supply of DEP to the surface is interrupted, this boundary becomes immobile, and the concentration of DEP in the swollen layer is that which is just sufficient to saturate residual un-nitrated hydroxyl groups on the NC. Reducing the activity of the DEP by admixture with benzene results in similar sharp boundaries, presumably because capillaries become blocked with spent diluent. Apart from capillary action, movement is always perpendicular to the fiber axis.
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  • 80
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    Journal of Applied Polymer Science 27 (1982), S. 2857-2867 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Partially oriented poly(ethylene terephthalate) yarns (PET POY) have been studied with respect to their birefringence, sonic modulus, and stress-optical properties in an effort to extract the values for the intrinsic birefringences of the crystalline (Δnc°) and amorphous (Δna°) regions. The data have been analyzed within the framework of both the sonic modulus-birefringence treatment of Samuels and Dumbleton, and the Gaussian rubber elasticity theory using the usual shrinkage stress-birefringence relations. The following values have been determined: Δnc° = 0.22 and Δna° = 0.19. The work was undertaken to resolve the discrepancy in the published literature values of these two parameters.
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  • 81
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    Journal of Applied Polymer Science 27 (1982), S. 2919-2931 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Several neat and reinforced epoxy resin formulations were prepared and investigated. Solid glass microspheres, with and without coupling agent, were used as reinforcement. After completion of post-cure all samples were quenched into an ice-water bath. Upon removal from the ice-water bath, dynamic mechanical and fracture properties of all samples were evaluated as a function of time elapsed after quenching. Electron microscopic evidence was obtained for the existence of nodular morphology in all cured systems. The changes in dynamic mechanical and fracture parameters, induced by the sub-Tg annealing, were described in terms of the model of inhomogeneous thermoset morphology.
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    Journal of Applied Polymer Science 27 (1982), S. 1827-1832 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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    Journal of Applied Polymer Science 27 (1982), S. 1849-1851 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 84
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    Journal of Applied Polymer Science 27 (1982), S. 1897-1902 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Photoresponsive polymeric adsorbents containing an azobenzene moiety were prepared, and adsorption behavior of lysozyme onto the adsorbents was studied. In the dark the amount of lysozyme adsorbed increased with increasing hydrophobicity of the surface of the adsorbents. Therefore, it is suggested that hydrophobic interaction between lysozyme and the adsorbents plays an important role in their adsorption behavior. On irradiation with UV light, the amount of lysozyme adsorbed decreased. This result is due to increased polarity of the surface of the adsorbent induced by UV irradiation and the resultant reduction in hydrophobic interaction with lysozyme. When a column chromatography of lysozyme was carried out using the photoresponsive polymeric adsorbent as a packing material, lysozyme was eluted by photoirradiation in a system using water as the single solvent.
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  • 85
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    Journal of Applied Polymer Science 27 (1982), S. 1933-1944 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: In order to study modifications of the properties of a polyurethane adhesive, we have prepared polyblends with a siliconic polymer and mixtures with some fiber reinforcing agents or with plasticizers. Stress-strain measurements were done on the samples using an Instron Model 1125 Universal testing machine. For comparison, some specimens were kept at normal room conditions, while others were cycled in an artifical weathering chamber. Results are discussed and conclusions drawn.
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    Journal of Applied Polymer Science 27 (1982), S. 1967-1975 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Charge stabilities of various polar polymer homoelectrets were determined. Although these electerts are reasonably stable in dry environments, they rapidly discharge when exposed to humidity. The rate of charge decay was found to depend directly on the ability of these polymers to absorb water under equilibrium conditions. Protection from humidity is obtained if these polar polymers are coated on both sides with nonpolar polymers. If, however, two different polymer films are laminated, the electret behavior follows a pattern that can be explained on the basis of charging at the interface. Difference in stabilities of the electrets of polar and nonpolar polymers is attributed to the differing natures of the charge traps present in these two classes of polymers.
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    Journal of Applied Polymer Science 27 (1982), S. 2015-2023 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: From a study of the oxidation of bisphenol-A epoxy resin cured with DDM (4,4′-diaminodiphenylmethane), it has been shown that the development of greenish-blue colors is due to an initial reaction between molecular oxygen and secondary amine groups. A full reaction scheme is suggested and supporting evidence, in the form of UV/visible, infrared, and ESR spectra, is presented.
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    Journal of Applied Polymer Science 27 (1982), S. 2043-2052 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: As a first step in the elucidation of the microstructure of styrene copolymers using ultraviolet spectroscopy, the data available in the literature has been reviewed and reevaluated. It is shown by using simple error propagation analysis that the abnormalities observed in the extinction coefficients of styrene copolymers can be easily attributed to the experimental error. No significant deviations from the linear absorption behavior can be observed at the specific wavelengths reported in the literature (254-269 nm). As a result of this work, a useful set of correlations for the estimation of the copolymer composition have been obtained. These correlations appear to be adequate for copolymers of different microstructure.
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  • 89
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    Journal of Applied Polymer Science 27 (1982), S. 2091-2103 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Preoriented isotactic polypropylene was used to clarify the molecular process in zone-drawing with which the necking part is confined in a thin heating zone during uniaxial drawing. The process was analyzed on the basis of rate process, the mechanical properties of zone-drawn samples, and the superstructural change during zone-drawing. The values of activation energy for deformation, ΔH*, and the activation volume, ΔV*, were affected by the deformation mechanisms preferentially taking place during the zone-drawing. The attainable maximum modulus of zone-drawn sample at θ = 45° was larger than those at θ = 0° and 90°. The highest strength was also obtained at θ = 45°. The values of modulus and strength strongly depended on both the orientation function of the crystal c-axis and the orientation function of amorphous chains. In the region of a very high zone-drawing rate, in which microcracks are preferentially formed, both modulus and strength decreased, whereas they increased with increasing the zone-drawing rate below this region, giving the optimum condition for achieving the maxima in the modulus and strength.
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    Journal of Applied Polymer Science 27 (1982), S. 3019-3025 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The thermomechanical behavior of particle composites was investigated in their transition region. In particular, the value of the glass-transition temperature Tg, which constitutes an upper limit for the structurally important glassy region, was examined. According to experimental evidence existing in the literature the introduction of a reinforcing filler in a polymeric matrix causes Tg of the latter to increase, unless mechanical imperfections counterbalance the reinforcing effect or even produce a Tg for the composite which is lower than that of the matrix. Based on mechanical theories, valid for the mechanical moduli of viscoelastic particle composites, a model was introduced that explains why the glass transition of composite materials may be reduced in some cases, whereas it may be increased in others. The concept of interphase between inclusions and matrix was used for the development of the model. Interphase is assumed to be a region, which is created between the matrix material and the filler particles, both considered as homogeneous and isotropic, whose thermomechanical properties and volume fraction may be determined from the overall thermomechanical behavior of the composite.
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  • 91
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    Journal of Applied Polymer Science 27 (1982), S. 3067-3077 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A perturbation chromatography apparatus has been designed and constructed for determining the vapor-liquid equilibrium between a two-component (solvent/helium) vapor phase and a two-component (polymer/solvent) liquid phase. The apparatus performed very well, giving reproducible and reliable results that agree with independent, previously reported studies. All tests of the equipment indicated that it was successful in meeting the conditions of low column pressure drop, small perturbations, and slow flow rate that are required for perturbation chromatography. Binary polymer/solvent data were obtained for polybutadiene (PBD)/benzene or polybutadiene/cyclohexane systems at solvent partial pressures to 40 kPa and for n-hexane at infinite dilution, all at the three temperatures of 333.15, 355.00, and 373.15 K. The experimental data for each system can be represented within experimental error by the Flory-Huggins polymer solution theory using a single binary interaction parameter that is independent of temperature and concentration.
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  • 92
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    Journal of Applied Polymer Science 27 (1982), S. 2209-2228 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The nature of the deformation process involved in hot drawing of porous high-molecular-weight polyethylene was examined by apparent elongational viscosity measurements at drawing temperatures between 100°C and 150°C and deformation rates in the range of 10-6-10-3 m/s. The temperature dependence of the apparent elongational viscosity revealed three distinguishable intervals with different activation energies. In the range of 100-133°C, the activation energy amounted to 50 kJ/mol, indicating that hot-drawing in this region proceeds by a sliding motion of separate fibrillar units. The interval between 133°C and 143°C was characterized by an activation energy of about 150 kJ/mol. Moreover, the porous character of the polyethylene fibers was found to decrease in the drawing process above 133°C. These observations were ascribed to an aggregation of the elementary fibrils upon hot-drawing due to partial melting at the surface of the fibrils. At temperatures above 143°C the activation energy was strongly affected by the initial morphology and the draw ratio of the fibers and amounted to values in the range of 200-600 kJ/mol. Molecular orientation in this region is accomplished by a slippage of individual chains, with entanglements acting as semipermanent crosslinks. Decreasing of the rate of elongation in the drawing process resulted in premature fiber breakage, indicating that the crosslinking action of the entanglements is limited by the time scale of the process.
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    Journal of Applied Polymer Science 27 (1982), S. 2369-2375 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Influence of drawing velocity on morphological parameters of nylon-6, PET, and PBT filaments has been studied. The drawing was carried out at approximately 20°C above the effective glass transition temperature of these materials. The results are explained in terms of drawing-induced changes in temperature and in rate of crystallization.
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  • 94
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    Notes: Poly(methyl methacrylate) has been grafted onto mulberry silk in an aqueous medium by using potassium peroxydiphosphate-cysteine (PP-Cys) redox initiator. Various effects upon grafting such as concentration of cysteine, concentration of peroxydiphosphate, concentration of monomer, concentration of sulfuric acid, and temperature were studied. At a low range of cysteine concentration (6.25 × 10-4 mol/L), the rate of polymerization Rp (%/s) is proportional to cysteine concentration and the exponent is calculated to be 0.8. The monomer exponent is calculated to be unity up to the concentration of 65.72 × 10-2 mol/L. From the Arrhenius plot of log Rp vs. 1/T (T = absolute temperature) the overall activation energy is computed to be 15.19 kcal/mol. A suitable kinetic path has been pictured and a rate expression has been derived.
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  • 95
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    Notes: The cellulose/lithium chloride/dimethylacetamide (DMAc) and cellulose/lithium chloride/N-methyl-2-pyrroilidinone (NMP) solutions were investigated by 13C NMR spectroscopy. Well-resolved spectra were obtained for both solutions and indicated that cellulose was present in these systems in the form of underivatized cellulose. The change in 13C chemical shifts of DMAc and NMP in the presence of LiCl and LiBr was compared with that of several salt/aprotic solvents, and the results point to the existence of a cellulose-LiCl-DMAc (or NMP) complex in which the lithium cation is strongly bound to the amide carbonyl oxygen and the chloride anion involved in the dissociation of the cellulose hydrogen bonds. Spin-lattice relaxation times (T1 of the 13C carbons of the solvent molecules, DMAc and NMP, show a large decrease in T1 for all solvent carbons upon addition of LiCl. Further decrease in T1 is observed when cellulose is introduced to the LiCl/NMP but not to the LiCl/DMAc systems. These observations are attributed to slower molecular motions of DMAc and NMP in the presence of LiCl, and, in the case of NMP, in the presence of cellulose.
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    Journal of Applied Polymer Science 27 (1982), S. 2475-2482 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: In low-density polyethylene containing the additive propylfluorancene, radiation energy received by polyethylene is transferred to propylfluorancence, and the production of radicals at 77 K in polyethylene is suppressed. Propylfluoranncene also increases the rate of the decay of radicals of polyethylene at room temperature. The depression of radical production and accelaration of radical decay at room temperature results in the depression of gas production and crosslinks at room temperature in low-density polyethylene containing propylfluorancene. Similar results were obtained in ethylen-propylene copolymer containing the same additive.
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    Journal of Applied Polymer Science 27 (1982), S. 2797-2807 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Thioetherglycidyl resins produced by condensation of bis(4-mercaptophenyl)ether and bis(4-mercaptophenyl) methane with epichlorohydrin were obtained by heterophase alkaline condensation. To define the optimal conditions of condensation, the following factors that influence the process were studied: the kind of organic phase and the mole ratios of epichlorohydrin:mercaptan, alcohol:mercaptan, and alkaline hydroxide:mercaptan. For all syntheses yield and the epoxide content were found. The structure of thioetherglycidyl resins with the highest epoxide content was determined by elementary analysis, infrared IR, and NMR spectra. The physical and chemical properties were also defined. The investigations covered the determination of some properties of resins, cured chemically or thermally with different curatives and thermal and mechanical properties of the cured compounds.
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    Journal of Applied Polymer Science 27 (1982), S. 2869-2883 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The glass-transition temperatures (Tg's) and specific heats (Cp) of poly(vinyl chloride) (PVC) and PVC plasticized with 5-120 phr di(2-ethylhexyl) adipate (DOA) and tri(2-ethylhexyl) trimellitate (TOTM) have been determined by differential scanning calorimetry (DSC). Measured Tg's were compared to predictions by the Couchman and Karasz (C-K) thermodynamic theory, three related empirical equations, and a new equation obtained from the C-K relation by assuming the product TgΔCp to be constant. It was found that the Tg's of the PVC/TOTM mixtures are adequately predicted only by the C-K and the derivative relation. The Tg's of the PVC/DOA mixtures follow a sigmoidal or cusp-like dependence on plasticizer composition as has been observed for some other PVC/plasticizer mixtures. In this case, the approximation afforded by the C-K or derivative equations is still superior to the empirical models over a wide composition range. Dynamic mechanical analysis of the PVC/DOA mixtures suggests that the DSC transitions may consist of two overlapping phase transitions. The reported sigmoidal composition dependence of the DSC Tg's may therefore result from the measured Tg's being weighted towards the temperature corresponding to the predominant dynamic mechanical transition (i.e., the high Tg phase at low plasticizer concentrations and the low Tg phase at high plasticizer concentrations). In such cases of partial phase separation, the C-K or the derivative equation may be used to estimate the composition of the two phases at each overall plasticizer concentration.
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    Journal of Applied Polymer Science 27 (1982), S. 2885-2890 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A new application of low-angle laser light scattering has led to a new instrument capable of characterizing the rubber particle size distribution of high-impact polystyrene (HIPS) containing particles as small as 0.1 μ. Rubber particle size distributions of several HIPS resins have been characterized, and the particle size ranking of resins using light scattering parallels the ranking of resins using photomicroscopy. Several solvents have been employed to suspend the HIPS rubber particles for the scattering determination. Swelling of the rubber phase has been found to be relatively insensitive to variations in rubber phase crosslinking when methyl ethyl ketone is used to suspend the rubber particles. Particle swelling in methyl ethyl ketone does not detract from the usefulness of the light scattering method for HIPS rubber particle size characterization.
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    Journal of Applied Polymer Science 27 (1982), S. 2997-3005 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The sorption and transport of several gases in poly(phenylene oxide) were measured at 35°C, and the results have been analyzed in terms of the dual sorption/mobility models which have been successfully employed for this purpose for other glassy polymers. Both the extent of sorption and rate of permeation of gases are quite large for poly(phenylene oxide) compared to other glassy polymers with rigid chain backbones. It is shown that the high extent of sorption is owing to the high glass transition temperature of this polymer, but this is not a significant factor in its high permeability to gases. The latter stems from large diffusion coefficients. It is shown that the capacity of the Langmuir mode of sorption inherent to glassy polymers is related to the value of the glass transition temperature in a general way for a wide variety of polymers. Observations about the diffusion coefficients for numerous gas-polymer pairs are discussed.
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