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  • Articles  (2,359)
  • Chemistry  (2,359)
  • Cell & Developmental Biology
  • 1955-1959  (2,359)
  • Physics  (2,359)
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  • Articles  (2,359)
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  • 1
    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 number of fluorinated polyesters have been prepared by condensing hexafluoropentanediol with one or more dibasic acid chlorides, and melting and glass transition temperatures and rates of crystallization have been determined, largely by means of volume dilatometry. The relation between [η] in chloroform at 30° and M̄n for hexafluoropentylene adipate (HFPA) was found to be [η] = 3.20 × 10-5 M̄n. The melting point Tm was found to increase from 34.5° to 104° as the isophthalate content in a series of adipate copolyesters increased from 0 to 100 mole-%. The glass transition Tg increases from -57° to -31° as isophthalate content increases from 0 to 50 mole-%. Tg is raised about 6° by the crosslinking of the polyesters. Rates of crystallization were determined for two HFPA samples with M̄n's of 13,000 and 19,500. Maxima in these rates occurred at about -13° and -15°, respectively. Respective t½ values for (linear) HFPA, vulcanized HFPA, and a copolyester containing 20 mole-% isophthalate are 48, 1140, and 27,200 min., respectively, at -10°. All the crystallization isotherms conform to Avrami's equation, (Vt - V∞)/(Vt - V∞) = exp {-αt″} for n = 6 over the initial stages of the process. At 1° both HFPA isotherms agree with the above equation over a large part of the process; however, as the isotherm temperature decreases, the equilibrium degree of crystallinity, as judged by the overall specific volume change, decreases and the isotherms diverge from Avrami's equation over progressively larger portions of the process. The product of the maximum rate of crystallization for each isotherm with either t½ or τi, the “induction time,” decreases with decreasing temperature, as would be expected in view of Avrami's equation. The value of 6 observed for n, a constant determined by the nucleation and growth mechanisms, is anomalous since only values of 1 to 4 are theoretically predictable. Values over the range of 1 to 4 have been observed experimentally by other workers for a variety of polymers.
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  • 2
    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 study was made of the dilute solution properties and the molecular weight distribution of a polyurethane polymer prepared from polypropylene glycol 2025 and toluene-2,4-diisocyanate by a bulk polymerization under anhydrous conditions at 60°C. Such conditions were chosen to minimize possible side reactions which could produce branching. The polymer, which had a weight-average molecular weight of 36,500, was separated into fourteen fractions by fractional precipitation from a benzene solution with isooctane as precipitant. The fractions were characterized by light scattering measurements on methanol solutions and by dilute solution viscosities in methanol, benzene, and a theta-solvent. The molecular weight distribution of the unfractionated polymer and the relations between molecular weight and intrinsic viscosity in the various solvents were determined. Polymer configurations and interaction parameters are discussed.
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  • 3
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 1 (1959), S. 310-312 
    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 reactivity of hydrofluorocarbon polymers toward organic amines increases, generally, with increasing fluorine content and with increasing basicity of the amine. The position of fluorine in the molecule with respect to hydrogen strongly affects the electrophylic character of the hydrogen atom. A discussion of the effects of neighboring groups on this reactivity is presented.
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  • 4
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    Journal of Applied Polymer Science 1 (1959), S. 323-328 
    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 the emulsion polymerization of methyl methacrylate have been examined in the light of recent advances in theory. It has been found that, if allowance is made for the decrease in the termination rate, the kinetics of the reaction can be predicted up to the point where all monomer is absorbed by growing monomer-polymer particles. In order to do this it must be assumed that the efficiency of initiation is low and is a function of the size and number of growing particles in the latex. A possible explanation for these observations is discussed.
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  • 5
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    Journal of Applied Polymer Science 2 (1959), S. 86-92 
    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 thermal-oxidative degradation of films of poly(ethyl acrylate) about 35 μ thick were studied in the temperature range of 80 to 120°C. The degradation was followed by determining intrinsic viscosity changes, absorption of oxygen, and production of titratable acidity in the polymer. From viscosity results an apparent activation energy of 28.6 kcal. was calculated. Only very slight degradation occurred when the polymer was heated in a vacuum. In air, the reaction is inhibited by the presence of hydroquinone, while the addition of benzoyl peroxide caused a rapid degradation even in a vacuum. The rate of oxygen absorption was found to be similar to that typical of autocatalytic oxidations. Oxygen diffusion did not appear to be the rate-determining factor in the degradation of films 10 to 70 μ thick. The weight loss during degradation was very small, but infrared and mass spectra indicated the presence of carbon dioxide, ethanol, formic acid, and water among the volatile products. A degradation mechanism based on hydroperoxide formation and decomposition is suggested.
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  • 6
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    Journal of Applied Polymer Science 2 (1959), S. 100-107 
    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 detailed analysis of the factors operating in polymer fractionation by gradient elution column methods is offered. A comparison between experimental fractionations of a range of polystyrenes indicates that the most important single factor is the concentration of polymer permitted in the eluant. For the logarithmic composition gradient considered here, the average concentration in the eluant may be controlled through control of the volume of the eluant in the mixing vessel. This volume should be not less than 200 times the volume of the polymer sample, and considerably larger if the polymer is of high molecular weight.
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  • 7
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    Journal of Applied Polymer Science 2 (1959), S. 120-122 
    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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  • 8
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    Journal of Applied Polymer Science 2 (1959), S. 122-123 
    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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  • 9
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    Journal of Applied Polymer Science 2 (1959), S. 126-126 
    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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  • 10
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    Journal of Applied Polymer Science 2 (1959), S. 127-127 
    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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  • 11
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    Journal of Applied Polymer Science 2 (1959), S. 127-128 
    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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  • 12
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    Journal of Applied Polymer Science 2 (1959), S. 163-165 
    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: Supporting evidence for the electron bombardment mechanism for the degradation of dielectric materials by corona discharge has been obtained by correlating the maximum radius of oxidized product, oxalic acid, produced by corona discharge from a spherical electrode upon polyethylene, with the theoretical range of electrons produced. Rationalizations concerning the formation of oxalic acid in the process are offered.
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  • 13
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    Journal of Applied Polymer Science 2 (1959), S. 155-162 
    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: Diisocyanates condense readily with hydrazine or hydrazine hydrate to give polyureylenes with the structure: \documentclass{article}\pagestyle{empty}\begin{document}$$ \left[ \hbox{---} {\rm R} \hbox{---} {\rm NHCONHNH} \hbox{---} {\rm CONH} \hbox{---} \right]_x $$\end{document} Similarly, dihydrazides (NH2NH—COR′CONHNH2) condense with diisocyanates to give polymers with the structure: \documentclass{article}\pagestyle{empty}\begin{document}$$ \left[ \hbox{---} {\rm R} \hbox{---} {\rm NHCONHNH} \hbox{---} {\rm COR'} \hbox{---} {\rm CONHNHCONH} \hbox{---} \right]_x $$\end{document} Tough films and fibers can be prepared from these polymers by conventional techniques. Solutions of some of these polymers are relatively unstable at elevated temperatures, the polymer apparently reverting to starting materials. Attempts to stabilize the solutions were unsuccessful.
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  • 14
    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 the investigation of the rheological properties of viscoelastic material, a variety of instruments may be employed. The investigation may be concerned either with mechanical properties under “steady-state” or dynamic conditions or with optical properties such as are determined by flow birefringence techniques. This paper describes representative instrumentation (available at the Franklin Institute Laboratories) suitable for making the above types of determinations. The types of instruments are: (1) a coni-cylindrical rotational viscometer, (2) a high-pressure capillary tube viscometer; (3) the Weissenberg rheogoniometer, (4) a jet extrusion instrument, (5) a vibration tester, (6) a torsion crystal instrument, and (7) a flow birefringence instrument. The fundamental principles underlying the instruments which have not been described previously, are discussed.
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  • 15
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    Journal of Applied Polymer Science 2 (1959), S. 181-185 
    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: Differential spectra have been obtained of a number of irradiated polyamides and monomeric amides. These spectra indicate that both free radical and molecular products are produced as primary products. The transient colored products (which are believed to be free radicals) and molecular products appear to be in the amine portion of the molecvle for the most part. The approximate G yield for radical production in nylon 66 is 5.8, and the approximate molar extinction coefficient of the free radical at 355 mμ is 690.
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  • 16
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    Journal of Applied Polymer Science 2 (1959), S. 66-70 
    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: Crystallization and orientation of isotactic polypropylene film by stretching were investigated. The specimen used was a film of thickness 0.03 mm. and had ca. 30% crystallinity in the initial state. It was observed both by x-ray examination and measurement of density that the crystallization of the stretched film increased proportionally to the stretching ratio. And it was confirmed that a quasi-crystalline structure was already developed in the low stretching ratio coexisting with the ordinary stable crystalline structures. This quasi-crystal structure can be easily transformed into the ordinary stable state at above 100°C., as well as the quasi-crystal structure in melt spinning filament, as described in a previous paper. It was also confirmed that the ordinary stable crystalline part was biaxially oriented by high stretching at room temperature, that is, (110) plane of the crystallite was preferentially oriented perpendicular to the surface plane of the film in the cross section perpendicular to the stretching axis. This phenomenon was elucidated from both the cohesive interactions between lattice planes and the compressive stress in the stretching process.
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  • 17
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    Journal of Applied Polymer Science 2 (1959), S. 71-80 
    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 elongation of polyvinyl alcohol and of formalized polyvinyl alcohol films under constant load for a wide range of conditions of temperature and humidity seems to be affected predominantly by the diffusion of water molecules into these polymeric films, as these films have many water-sensitive bonds. In order to obtain a perspective of the diffusion mechanism of water molecules into these polymer films, the theoretical analysis of creep curves is here worked out. Since the diffusion is a time-dependent, non-Fickian process, the time dependence of the diffusion coefficient is considered into our theoretical treatment. It is also assumed that the elongation is caused only by the breaking of hydrogen bonds due to the absorption of water molecules in amorphous regions of the polymer film.To evaluate theoretical equations for the creep curves in accordance with a simple Voigt model, the parameter α for the rate of diffusion is conveniently substituted for by K, the parameter for the rate of elongation. Experiments were performed at temperatures from 20 to 50°C. at 60% R. H., and also at different relative humidities ranging from 40 to 80% at a constant temperature of 30°C. A series of creep curves for PVA and PVF, the latter having a degree of formal substitution ranging from 6% to 42.5% were obtained.In analyzing the observed creep curves by the present theoretical treatment, we can easily compute the values of K through application of the condition for the characteristic inflection point of each curve, i.e., d2γ/dt2 = 0. By use of the values of K thus obtained and by application of the theory of absolute reaction rates, the activation energy and entropy for the diffusion process of water molecules are duly determined. The values thus obtained are also compared with those calculated by Hauser and McLaren. The activation energy and entropy are highest and lowest, respectively for PVF (6%); this is made adequately explicable by the fact that the proportion of amorphous polymer in these films is found to be maximum when the degree of formalization is between 10 and 20%.
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  • 18
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    Journal of Applied Polymer Science 2 (1959), S. 93-99 
    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: Glass transition phenomena in several polymers were studied by dielectric and dilatometric measurements. The dielectric measurements were made over the frequency range of 10-4 or 10-1 to 106 cycles/sec. and the temperature range of the glass transition. In the dilatometric study, volume relaxation curves and volume vs. temperature curve were obtained. The transition in three amorphous polymers, (polyvinyl acetate, polystyrene, and polymethyl methacrylate), depends upon frequency or rate of cooling and seems to be an apparent transition. In three crystallizable polymers, (vinylidene chloride-vinyl chloride copolymer, polyethylene terephthalate, and polyacrylonitrile), the magnitude of the dielectric absorption decreases steeply with decreasing temperature in the transition range, and the transition by the volume expansion remains when equilibrium is attained. The transition in the three crystallizable polymers seems to be a real one. Temperature dependences of the activation energies of the dielectric relaxation processes have been described.
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  • 19
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    Journal of Applied Polymer Science 2 (1959), S. 216-224 
    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 force required to peel an aluminum (or nickel) ribbon glued to a rigid glass plate with a polyethylene or polyvinyl acetate was determined. It proved to be smaller than expected (from a theory, partly new) both for adhesives which were almost Hookean solids and for those whose stress-strain curve could approximately be represented as stress = const. (strain)0.5. In the latter group, the difference between the theory and the experiment was due to stress concentrations at the right-hand and the left-hand edges of the adhesive layer; these stress concentrations formed because, when a pull was applied, the adhesive contracted in the directions perpendicular to that of pull. As a consequence of this effect, the peeling force W0 was not proportional to the width w of the ribbon; sometimes, a linear relation W0 = aw + b seemed to be valid. On the other hand, near-Hookean adhesives of a low total elongation required a peeling force proportional to w; the stress concentration dangerous for these materials occurred at the boundary between the adhesive and the bent ribbon at the sharp bend. The damage to the brittle adhesive caused by the ribbon deformation could be reproduced without bending, namely by extension of the ribbon beyond its yield strength.
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  • 20
    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: Polyethylene films and sheets were oxidized in oxygen, air, or aqueous nitric acid at temperatures up to 100°C., and the decay of physical properties was measured by mechanical testing. In some instances, weight change and volume of oxygen absorbed were reliable indexes of the physical degradation as measured by a particular property such as ultimate stress or ultimate elongation, but they were unreliable in comparing the degradation of different types of polyethylene. Although the more crystalline polyethylenes absorbed less oxygen than branched polyethylenes, the former degraded more rapidly in air at 100°C. In degradation by air or oxygen, exposure time affected the ultimate elongation more than it did ultimate tensile strength. In nitric acid the reverse was true. The yield elongation and the yield stress were virtually unaffected by any of the degradation methods unless the exposure was very long. A preferential oxidation of the noncrystalline regions is proposed to account for this result. The appropriateness of any tensile property as a measure of degradation is concluded to depend on the intended use of the plastic.
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  • 21
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    Journal of Applied Polymer Science 2 (1959), S. 236-240 
    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 absorption of glycerol solutions by cellulose regenerated from viscose has been studied over a range of glycerol concentrations up to 95%. After corrections had been made for loss of moisture in handling, only very small differences between the concentration of glycerol in the film and the concentration of glycerol in the equilibration bath were found. The enrichment factor (defined as the ratio of glycerol concentration in the film to the glycerol concentration in the bath) was unity up to 16% glycerol, reached a maximum of 1.03 at approximately 25% glycerol, and fell to 0.96 at 95% glycerol concentration. We concluded therefore that glycerol and water are absorbed by gel cellulose in practically the same ratio as they occur in the bath solution and no preferential affinity for glycerol over water is evident. Two cellulose films of different degree of polymerization gave similar results. A redetermination of refractive indexes of aqueous glycerol solutions at 25° is included.
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  • 22
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    Journal of Applied Polymer Science 2 (1959), S. 241-245 
    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: Eight organic coating films were removed from their metal substrates by two very different methods and were examined by means of water vapor adsorption isotherms. The data obtained in this study reveal the rates of adsorption, the relative pressure required to form a monolayer, the number of active sites for water vapor adsorption, and the parameters in the classical BET isotherm equation. Removal of the films by electrolysis in an alkaline bath and by amalgamation of the tin plate produced films of considerably different structure. Since the electrolysis procedure subjects the film to mechanical and possibly chemical alterations, it is proposed that the increase in water vapor adsorption by the former type of films is the result of decreased crystallinity. Consequently, the films removed by amalgamation are considered to be more similar in total structure to the original films.
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  • 23
    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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  • 24
    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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  • 25
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    Journal of Applied Polymer Science 2 (1959), S. 255-256 
    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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  • 26
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    Journal of Applied Polymer Science 2 (1959), S. 257-263 
    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: Departures from behavior predicted by the statistical theory of rubberlike elasticity, which occur at high extensions, are ascribed to the finite extensibility of network chains. By use of a non-Gaussian statistical theory, a relation is obtained between the extension ratio λ*, the extension at which departures are small but significant and the degree of crosslinking. Experimental results on the dependence of λ* on the degree of crosslinking and on the degree of swelling are in good agreement with theoretical predictions. It is shown that the additional determination of λ* permits the calculation of both the degree of crosslinking and the extent of network flaws due to chain ends, from a single simple extension stress-strain curve. The calculation of these two basic parameters has hitherto been unattainable from measurements on vulcanized rubbers alone. This development provides a new technique of particular value in studies of the degradation of vulcanized networks.
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  • 27
    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: As evidenced by formation of peroxides and carbonyl, reaction occurs during the oxidation induction period of polyethylene. The meaning of the term oxidation induction period is revealed by the tremendous change in melt index, carbonyl, density, color, tensile, and elongation occurring towards the end of this time period. Hydroperoxide forms long before the end of the oxidation induction period even in the presence of an antioxidant. At any temperature both chain scission and crosslinking occur simultaneously. The rate of oxidation is accelerated by increasing temperature, unsaturation, and branching. Molecular weight seems to have no effect.
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  • 28
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    Journal of Applied Polymer Science 2 (1959), S. 264-272 
    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 mechanism of water transport across cellulosic membranes under high pressure differentials was studied in an attempt to explain the semipermeability of these films when used as osmotic membranes for ionic solutions. Diffusion coefficients and activation entropy values for the diffusion of water and other fluids through various polymer films were determined, and compressive deformation of cellulose acetate and cellophane films was measured. Activation entropy values for the diffusion of water across both cellulose acetate and cellophane films illustrated that water molecules are constrained to states of high order as they are transported across the membrane under high pressure differentials. Activation entropy values for the diffusion of methanol through cellulose acetate film failed to support the proposition that chains of this polymer may actually be crosslinked by hydrogen-bonded water. It appeared, rather, that but one hydrogen of the water molecule was involved in hydrogen bonding to the polymer. A significant reorientation of the polymer in the pressure interval in which cellulose acetate film is induced into a semipermeable condition was indicated by pressure-dependent fluctuations of diffusion coefficients and activation entropy values in this interval. The greater elastic modulus of wet cellulose acetate film under a compressive force applied normal to the film surface demonstrated a strong interaction between water and polymer chains in the cellulose acetate-water structure. The capacity of the film for bound water was also increased by repeated compression while wet. Wet cellophane films deformed plastically under compression. Crosslinking polymer chains of cellophane film with cupric ions prevented plastic flow and, at the same time, increased the semipermeability of the film for sodium chloride solutions.
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  • 29
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    Journal of Applied Polymer Science 2 (1959), S. 302-307 
    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: Cinnamic acid esters of poly(vinyl alcohol) and of cellulose are insolubilized by ultraviolet radiation. This response may be increased by the inclusion of simple organic compounds such as Crystal Violet carbinol and Michler's ketone. A method of measuring this response (in terms of a sensitivity value, S) based upon photographic sensitometry has been devised. Preliminary study indicates that an increase in S is accompanied by an increase in response to the longer wavelengths of light.
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  • 30
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    Journal of Applied Polymer Science 2 (1959), S. 297-301 
    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 changes in air pressure affect the thermal and oxidative degradation of a methylphenylsilicone was investigated as a function of time. A closed, gas-circulating system of 1500-cc. volume, incorporating a magnetic balance for following loss of weight in the sample, was employed. Finely ground samples were heated at 400°C. for 7 hours with initial pressures of air ranging from 700 to 50 mg. Hg. Mass spectrometric and infrared analyses identified the gaseous and the volatile products. At all pressures, low molecular weight silicones represented a major portion of the weight loss. Final weight losses in air approximated 10%, and approached, at the lowest pressure (50 mm.), the 7% observed in argon. Water and benzene were evolved, the latter at a rate that decreased with decrease in pressure. Traces of phenol, formaldehyde, propane, and higher molecular weight hydrocarbons were also given off. The evolution of carbon dioxide, carbon monoxide, methane, and hydrogen and the consumption of oxygen were followed in detail. Changes in air pressure from 700 to 300 mm. did not alter appreciably the rates of product evolution, oxygen consumption, and of weight loss. At lower presures (300 to 50 mm.), however, the molar ratio of the total noncondensed gases generated to total oxygen consumed increased, indicating a possible change in reaction mechanism.
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  • 31
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    Journal of Applied Polymer Science 2 (1959), S. 318-321 
    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 method of continuous and intermittent stress relaxation measurements on rubber vulcanizates developed by Tobolsky and co-workers has been modified by the introduction of intermittent tangent modulus measurements during the continuous relaxation experiments. This allows rate of scission and crosslinking to be determined simultaneously and on the same specimen. The method is based on the use of small or moderate extension ratios α and on the fact that in this case the stress f in actual rubbers is represented more closely by the empirical relationship f = 3G(1-1/α) than by the theoretical f = G[α-(1/α2)], where 3G denotes Young's modulus at infinitesimally small strains.
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  • 32
    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 mechanism has been devised for the purpose of introducing a sudden strain of calculable amount into a viscoelastic fluid. The principle of the apparatus relies upon the deformation caused by the rotation of an elliptical sleeve about a flexible tube containing polymer solution. An apparatus has been constructed which can produce a 90° rotation (with consequent deformation) in the period of one millisecond. The detection of the strained state is accomplished by means of strain birefringence. In this way, relaxation can be studied in concentrated solutions for a time range beyond one millisecond.
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  • 33
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    Journal of Applied Polymer Science 1 (1959), S. 3-10 
    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: Gehman cold-flex, volume-temperature, and stress-temperature studies were used to investigate the low-temperature characteristics of polysiloxane copolymers with respect to copolymer composition. A complete range of phenyl methyl-dimethyl siloxane copolymers were examined as elastomeric compounds. Like other copolymers, the stiffening temperature was dependent upon the composition of the copolymer. Stiffening of the elastomers was due to crystallization in some cases and second-order transition in others. Copolymers having either low or high amounts of PhMeSO stiffened because of crystallization, while copolymers of intermediate composition (7.5 to 15 mole-% PhMeSiO) stiffened because of nearness to their respective second-order transition temperatures. Second-order transition temperature increased with the PhMeSiO content. For those siloxane polymers and copolymers that crystallized, the process was rapid when compared with crystallization behavior of other polymer systems. Only one minimum low-temperature stiffening point was found in the phenyl methyl-dimethyl siloxane copolymer system. The unique low-temperature characteristics of polysiloxane elastomers are explainable on the basis of three factors. These are: (a) very flexible molecules, (b) low temperature coefficient of viscosity over a broad temperature range including low temperatures, and (c) copolymerizability of dimethyl siloxane with other siloxanes containing bulky pendant groups which lower the stiffening temperature.
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  • 34
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    Journal of Applied Polymer Science 1 (1959), S. 24-27 
    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: Domains, or areas of inhomogeneities and imperfections, may be made visible in polystyrene by treatments of the plastic with certain liquids and vapors. Different types of domains are revealed by different techniques, depending upon the solvent power of the liquids and vapors. One type of domain reveals itself as craze cracks when polystyrene is first soaked in a nonsolvent such as methanol, and then exposed to the vapors of a solvent such as hexane or benzene. A second type of domain may be revealed by exposing polystyrene to certain mixtures of solvents and nonsolvents which produce a rough, whitened surface on the polystyrene. For the first type of crazing, the size of the domains is influenced by the frozen-in thermal stresses, and the shape of the domains is influenced by molecular orientation. The domains of the second type are due to heterogeneity of molecular orientation and are not found in annealed specimens. A theory has been proposed which explains crack crazing in terms of adsorbed vapors in cracks and areas of imperfections in the polystyrene.
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  • 35
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    Journal of Applied Polymer Science 1 (1959), S. 37-42 
    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: About 3% by weight of carbon black adequately protects polyethylene against photo-oxidation and, under accelerated test conditions, slightly inhibits thermal oxidation. As a rule small amounts of organic antioxidants are also added to the polymer for optimum protection. Now many of the common phenolic and amine additives have been found to function much less effectively in polyethylene containing carbon black than in clear polymer. Loss of effectiveness is attributed to adsorption and/or decomposition of the antioxidant by both basic and acidic carbon black.
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  • 36
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    Journal of Applied Polymer Science 1 (1959), S. 56-62 
    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: High polymers of ethylene oxide have been shown to have a number of unique properties in water solution. In this study, these properties have been investigated from the view of the behavior of large neutral molecules in media of high dielectric constant. Predictably, these high polymers of ethylene oxide undergo salting-out effects which are reflected in changes of solution viscosity with salt concentration. Salts vary in effectiveness in a manner similar to that observed in the case of small neutral solute molecules. The salting-out and viscosity effects are paralleled by the inverse solubility-temperature relationship in water. Above a minimum molecular weight of about 50,000, the precipitation temperature (the temperature at which polymer separates from solution as a separate phase as the temperature is raised) becomes essentially independent of molecular weight. For these very high polymers the upper temperature limit of solubility in water is independent of polymer concentration over a wide range of concentration. These effects are discussed in terms of the balance of hydrophilic and hydrophobic character in the polymer structure which can be altered by increasing the hydrocarbon content of the polymer through copolymerization of ethylene oxide with other olefin oxides such as propylene oxide. This investigation permits the development of an interpretation of the unusual rheology of high molecular weight poly(ethylene oxide) in water solution.
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  • 37
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    Journal of Applied Polymer Science 1 (1959), S. 43-49 
    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: Common secondary aromatic amine and alkylated phenolic antioxidants lose much of their activity in polyethylene containing carbon black. In contrast their thioether derivatives provide more protection against oxidation than the sum of the separate contributions of carbon black and the sulfur compounds. Organic disulfides and some thio-ethers without amino or phenolic hydrogen also safeguard polyethylene from oxidation but only in the presence of carbon black. Likewise thiols are excellent protectants in combination with carbon black but not in clear polymer. Aliphatic thiols, disulfides, and their polymeric derivatives and related selenium compounds exhibit similar activity.
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  • 38
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    Journal of Applied Polymer Science 1 (1959), S. 179-184 
    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: Information is presented on those physical properties where measurement is greatly facilitated by thermal stability greater than previously known in polyoxymethylenes, and properties of a mechanical nature characteristic of high molecular weight polymeric materials. The high molecular weight polyoxymethylenes studied possess the characteristic properties of a semicrystalline material in the high molecular weight range. The melting point, stiffness, and tensile strength of these materials substantially exceed those for linear polyethylene, which suggests that the effective chain interactions are enhanced by ease of close packing of the chains. High density and high crystallinity are in accord with this picture.
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  • 39
    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 the thermal decomposition of the polyester, Laminac 4116, were investigated in air and argon at atmospheric pressure by means of a continuous recording thermobalance and by differential thermal analysis. Samples were heated from ambient temperature to 600°C. at rates of 5°/min. and 15°/min. In air and argon, decompostion commences at 200°C. and is complete at 550 and 450°C., respectively. Four modes of degradation in oxygen and two in argon are indicated from derivative plots of the thermogravimetric curves. The kinetics of reaction were evaluated by the method of Freeman and Carroll. In the presence of air, the initial stage of reaction appears to involve formation of an unstable hydroperoxide intermediate which undergoes rearrangement and degradation. The energy of activation was calculated to be 19 kcal./mole. An exotherm corresponding to this first stage of degradation is observed by differential thermal analysis. The second and third stages of reaction in air correspond approximately to the two stages in argon with respect to their endothermal nature and to the temperature regions over which they occur. Mass spectrometric and infrared analysis were employed for identification of gaseous and volatile products. The fourth stage of reaction in air appears to involve the oxidation of carbon to carbon dioxide. Mechanisms of reaction are proposed and discussed.
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  • 40
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    Journal of Applied Polymer Science 1 (1959), S. 107-113 
    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 theoretical treatment is given which predicts the behavior of a foamed elastic material on the basis of a model consisting of a network of thin threads. Two cases are considered: (1) small strains, and (2) finite compressions, when the major part of the deformation of the threads is attributed to buckling. The behavior is given in terms of Young's modulus of the matrix and the density of the foam. Measurements of the load-deformation relations for small tensile strains and finite compressions are described for natural rubber foams prepared from latex. A wide range of density is covered (0.09-0.57), giving a variation of compression hardness of about 100:1. Satisfactory agreement with theory is found for both the cases considered, indicating that the basic concepts of the structure and mode of deformation are correct.
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  • 41
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    Journal of Applied Polymer Science 1 (1959), S. 129-132 
    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: Polyethylene irradiated in the B.E.P.O. pile at Harwell has been found to acquire new mechanical properties. At a certain dose, polyethylene was found to behave like rubber.
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  • 42
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    Journal of Applied Polymer Science 1 (1959), S. 114-120 
    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: Samples of Ziegler-type polyethylene containing no additives were placed in a temperature-programmed oven, melted, and subsequently cooled at constant rates. Average spherulite size, based on the measurement of fifty spherulites, and impact strength by a falling ball method were determined for different cooling rates and for samples having weight-average molecular weights of 125,000 175,000, and 300,000. It was found that both the formation of a brittle structure and the growth of spherulites occur over the relatively narrow temperature range in which the molten polymer passes from the liquid to the solid state. The rate of spherulite growth is initially proportional to the square root of time, viz., diffusion controlled, but subsequently becomes linear with time. The spherulite growth rate decreases with increasing molecular weight. There is no change in spherulite size after aging six months at room temperature. The impact strength decreases with increasing average spherulite size; however, the lower the average molecular weight, the greater will be the impact strength for a given average spherulite size. The loss in impact strength is attributed to the rupture of amorphous chain strained by the formation and growth of spherulites.
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  • 43
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    Journal of Applied Polymer Science 1 (1959), S. 158-163 
    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 this, the first of a series of five papers, the historical development of formaldehyde polymers, beginning with the work of Butlerov and continuing through the investigations of Staudinger and his collaborators, is reviewed. Recent studies in these laboratories have led to thermally stable high polymers of formaldehyde. Initiators and the role of impurities in the polymerization are described. An explanation is offered to account for differences in thermal stabilities between old and new polymers. Esterification, by which further increases in thermal stability are achieved, is described. It is proposed that the generic term “acetal resin” be used to described high polymers that are composed of repeating oxymethylene units.
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  • 44
    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 primary objective of this investigation has been to explain why cellulose acetate behaves as a semipermeable membrane in saline water. To explain this phenomenon, two different mechanisms for the transfer to water and ions through cellulose acetate membranes were formulated. Those ions and molecules that cannot enter into hydrogen bonding with the membrane are transferred by hole-type diffusion. The rate of diffusion appears to be governed by a water-cellulose acetate structure. The reaction between water and the cellulose polymers to form bound water regions is favored by compressing the membrane. As pressure is applied on the membrane, more bound water is produced, which causes the rate of hole-type diffusion to decrease. On the other hand, those ions and molecules that can associate with the membrane and are transported through it by alignment-type diffusion. The formation of the water-cellulose acetate structure does not appreciably diminish the diffusion rate of water through the membrane. Cellulose acetate begins to behave as an effective semipermeable membrane in saline water when it is compressed sufficiently to retard greatly the diffusion of NaCl. Several types of experiments were conducted to support these hypotheses. The most important evidence was obtained from resistance experiments. The electrical resistances of specific ions was measured across cellulose acetate at various pressures by using permselective membranes to prevent migration of the ion of opposite charge. It was observed that the rate of diffusion of those ions that cannot combine with the membrane actually does decrease as the membrane is compressed. The rate of diffusion of H3O+, which can enter into hydrogen bonding with cellulose acetate, is much higher and is not appreciably reduced as the membrane is compressed. These resistance-pressure relationships are correlated with the semipermeability of the cellulose acetate.
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  • 45
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    Journal of Applied Polymer Science 1 (1959), S. 169-178 
    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: Stable, high molecular-weight polyoxymethylene resins show the room temperature x-ray crystalline patterns expected from early work on unstable or low molecular weight polyoxymethylene resins. High-temperature studies show the specific features of this resin to be: (1) disappearance of crystalline peaks at 180°C., and (2) a super-cooling of 15°C. (i.e., nucleation periods much greater than 15 minutes for temperatures above 165°C.). Studies utilizing optical birefringence show similar melting and freezing behavior. Birefringence studies show effect of quench temperature and melt time and temperature on the average spherulite size and appearance. Under suitable conditions, very large (1 mm. diameter) spherulites can be grown. The effect of variations in the fine structure (spherulite size, crystallite size, and degree of crystallinity) on mechanical properties of thin sections shows that: (1) an increase in crystallinity (by specific volume) gives higher moduli, higher yield strengths, and lower values of elongation to break; (2) smaller spherulites increase the ductility, or ability to retain ductility as the rate of strain of the test is increased; (3) changes in crystallite size over a twofold range have lesser effects on these properties.
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  • 46
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    Journal of Applied Polymer Science 1 (1959), S. 185-191 
    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: High molecular weight polyoxymethylenes are not soluble at room temperature in any of the hundreds of solvents or solvent systems tested. However, solutions can be obtained at elevated temperatures with a wide variety of solvents. Phenolic compounds are the most effective at temperatures of 50-100°C. At the other extreme of solubility, solvents are absorbed by the acetal polymer in varying amounts, depending on the crystallinity of the polymer and the cohesive energy density of the solvent. The absorption is concentrated entirely in the noncrystalline region of the polymer.
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  • 47
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    Journal of Applied Polymer Science 1 (1959), S. 212-226 
    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 general mathematical approach to the rigorous treatment of experimental data on nonstationary-state diffusion in solids of complex shape is developed. The general solution for a uniform initial concentration, c0, and a constant surface concentration, cs, at times greater than zero is shown to be of the form \documentclass{article}\pagestyle{empty}\begin{document}$ \frac{{\bar c - c_s }}{{c_0 - c_s }} = 1 - \frac{2}{{\sqrt \pi }}\frac{S}{V}\sqrt {Dt} + \frac{{f^{''} (0)}}{2}\left( {\frac{S}{V}} \right)^2 Dt $\end{document} in the neighborhood of time zero, and \documentclass{article}\pagestyle{empty}\begin{document}$ \frac{{\bar c - c_s }}{{c_0 - c_s }} = \frac{\alpha }{{\beta ^2 }}\exp \left\{ { - \beta ^2 \left( {\frac{S}{V}} \right)^2 Dt} \right\} $\end{document} in the neighborhood of time infinity, where c is the average concentration at time t; S and V are the surface area and volume of the solid, respectively; D is the diffusion coefficient; and f″ (0), α, and β are constants dependent on solid shape. The vacuum drying of wheat has been studied, and it is shown that, for the wheat kernel, f″ (0) = 0.588, α = 0.862; and β2 = 1.301. The diffusion coefficient is an Arrhenius-type function of temperature given by D = D0 exp {-E/RT} where D0 = 76.8 cm.2/sec. and E = 12.20 kcal./mole.
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  • 48
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    Journal of Applied Polymer Science 1 (1959), S. 227-235 
    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 method for obtaining the intrinsic dielectric constant and loss factor of dry cellulose fiber along the fiber axis was developed, and the dielectric properties of viscose rayon, Bemberg (cuprammonium rayon), and cotton sliver were measured over the frequency range from 500 cycles/sec. to 3 Mcycles/sec. and the temperature range from -60 to + 20°C. by using the mutual inductance bridge. Only one dispersion could be observed in this temperature and frequency range. Cole-Cole's circular are law could be satisfactorily applied to the data obtained, and the parameters of the are (∊0 - ∊∞) and β for the three samples could be determined at each temperature. The value of (∊0 - ∊∞), which is proportional to concentration of the dipoles contributing to the orientation, increased with rising temperature and reached a limiting value at about -20°C. The value of β relating to the width of the distribution of relaxation times also increased with rising temperature, showing a little rise in the degree of increase at temperatures above -20°C. On the other hand, the apparent activation energy for dipole orientation, as calculated from the temperature dependence of the dispersion frequency, reached a maximum around -20°C. All these facts suggest that some transition will take place in the neighborhood of -20°C. This temperature is not considered to be likely to be the glass transition temperature for dry cellulose, since -20°C. is too low for a primary transition in stiff molecules such as cellulose, and since the observed value of the apparent activation energy is too small to activate the segmental movement of the main chains. It might be possible to expect some secondary transition, probably of a thermodynamical nature, relating to the movement of local parts such as side chains, especially methylol groups on glucose residue, at about -20°C., though there is no other support for this expectation. Moreover, the effect of the fine structures on the dielectric properties is that the magnitude of (∊0 - ∊∞) at each temperature decreases in the order, viscose rayon 〉 Bemberg 〉 cotton sliver, and this order parallels that of the accessibility of the three samples. This fact suggests that the dipoles in the amorphous region and on the surface of the crystallite provide the chief contribution to this dispersion.
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  • 49
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    Journal of Applied Polymer Science 1 (1959), S. 336-339 
    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 for quantitative gas-absorption measurements is described and illustrated with drawings and photograph. A commercially available aluminium block heating unit, adapted to accommodate glass sample tubes, is mounted in an octagonal frame. Gas burets and leveling bulbs are supported on the frame to provide an apparatus for measuring volume changes at a given pressure. Data on rate of heatup and temperature distribution within a sample tube are given. The apparatus has been used primarily for volumetric oxygen-absorption measurements in studies related to the oxidation of rubber, but it is adaptable to studies involving other materials and other gaseous atmospheres at controlled temperatures. For example, studies have been made with polyethylene, epoxide coatings, and drying oils. The apparatus has also proved useful for curing polyurethanes under moisture-free conditions and for the vulcanization of rubber in a nitrogen atmosphere.
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    Journal of Applied Polymer Science 1 (1959), S. 340-350 
    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: Published data on the solubility properties and diffusion coefficients for water in polyethylene are critically examined and related to the permeability coefficients analyzed in a previous paper. The data examined in the present article are even more variable than the permeability data, the measured diffusion coefficients varying over a fourteenfold range. Solubilities vary less from specimen to specimen but do so in an order opposite to that of the diffusion coefficients. Accordingly the permeability coefficients vary much less than do the diffusion coefficients. In an examination of the permeation process, as it must occur through semicrystalline polymer films, it is demonstrated that a systematic error is introduced if permeation through such films is described by means of equations developed for homogeneous materials. The error has been evaluated by means of an electrical analog and equations describing diffusion in semicrystalline polymers are derived which complement those already in existence for diffusion in homogeneous polymers. By means of these equations it is shown that the variations in permeability and diffusion coefficients cannot be explained on the basis of reasonable variations in the amount of crystallinity between otherwise comparable polymers or by reasonable variations in the way in which the crystalline regions occur in the amorphous matrix. The conclusion previously reached to the effect that variations in the structure of the amorphous phase from specimen to specimen are responsible for irreproducible transport properties still appears valid.
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    Journal of Applied Polymer Science 1 (1959), S. 371-372 
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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 1 (1959), S. 372-373 
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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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  • 53
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    Journal of Applied Polymer Science 1 (1959), S. 329-335 
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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: Molecular weight distributions of homopolymer and graft polymer obtained from the gamma and photoinitiated polymerization of methyl methacrylate with natural rubber latex have been determined. Broad distributions were found with peaks of low and high molecular weight polymer. The distributions were insufficiently defined to make definite assignments to the speeds of the reactions involved but were not inconsistent with the mechanism proposed in an earlier paper from kinetic considerations. Details are given of the column fractionation apparatus employed.
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    Journal of Applied Polymer Science 1 (1959), S. 351-355 
    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 effect of antirads on the gamma radiation yields of scission in black loaded natural rubber stocks has been studied. The yield of chain scission has been measured by stress relaxation methods. The antirads were found to decrease the rate of chain scission, both in air and under nitrogen, with the antirad effectiveness being greater in the former case. The presence of oxygen accelerated the radiation induced chain scission. These results may be explained if it is assumed that (1) RO2 · radicals lead to chain scission more readily than do R · radicals, and (2) RO2 · radicals react with antirads leading to stabilized products more readily than do R · radicals.
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    Journal of Applied Polymer Science 1 (1959), S. 371-371 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 56
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    Notes: The softener content of regenerated cellulose film (gel film) in equilibrium with aqueous glycerol solution was found to be determined primarily by only two factors: the softener concentration of the solution and the volume of free space within the gel film. Volume changes of film in contact with 10% glycerol solutions are negligible. Preferential uptake of glycerol as the solution passes into the film is, at most, slight, amounting to no more than 0.04% at the concentration used. No evidence was found for a large enrichment within the gel film, as has been postulated, or for adsorption of glycerol on cellulose chains. The system, cellulose-glycerol-water, appears to be a polymer-liquid mixture brought to equilibrium principally by diffusion. It appears that at 10% concentration, glycerol and probably other organic compounds are taken in by gel film by a diffusion process in which the free water in the film is replaced by solution without appreciable enrichment or change in volume. Water contained in the interchain spaces of cellulose is simply exchanged for softener solution. The free volume of the film as determined by the cellulose structure and the degree of crystallinity remains essentially unchanged on softener uptake at the softener concentration studied.
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    Journal of Applied Polymer Science 1 (1959), S. 373-374 
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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 1 (1959), S. 374-376 
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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 1 (1959), S. 376-378 
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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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  • 60
    ISSN: 0021-8995
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    Notes: Degradation studies on poly-α-methylstyrene at 25°C. under vacuum and in hydrogen and oxygen were carried out with the use of a Co60 gamma source. The degradation results are explained as a random breaking of skeletal chain bonds accompanied by a depropagation of the resulting fragments. The termination step for depropagation is considered as a chain transfer of the degrading radical to the produced monomer cloud, the monomer radical thus formed repolymerizing to some extent prior to termination. The necessary relationships are derived which permit the evaluation of the G-value for bond scission, the kinetic chain length for depropagation from the resulting Mn and Mw values, and the unsaturation produced. The determined G-values for chain scission are 0.25 in vacuum and hydrogen, 0.16 in air, and 0.08 in oxygen, the gases being at a pressure of one atmosphere. The number of monomer units split off per break was found to be 100 in vacuum, 50 in hydrogen, and essentially zero in the presence of oxygen. It is believed that hydrogen and oxygen terminate the depropagating radical, reducing the kinetic chain length. The reduction in the G-value for chain scission in the presence of oxygen may be due to either recombination of the terminal peroxide groups formed or deactivation of the chain prior to cleavage. The G-values for volatile products at room temperature are listed, the important ones being G(H2) = 0.035 and G(CH4) = 0.003.
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    Journal of Applied Polymer Science 2 (1959), S. 174-180 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: A geometrical analysis is given of the tread motions occurring in the contact length of a rolling tire. Both the case of a free rolling wheel and that of a wheel under torque are discussed. We have derived expressions and curves for the relative slip and compressions which occur at the contact length for the two conditions. It is found that two important structural features control the nature of tread motions. These are the torsional rigidity of the sidewall and the compressibility of the tread. In addition, the implication of the analysis in tire design and performance are discussed.
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    Journal of Applied Polymer Science 2 (1959), S. 246-250 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Copolymers containing various amounts of acryloyl chloride were made with ethyl methacrylate, methyl acrylate, and styrene by bulk polymerization and by conversion of acrylic acid copolymers. Fibers and films of these polymers were crosslinked with ethylenediamine, and it was shown that increased crosslinking led to increased tenscity (at elevated temperature), modulus, zero strength temperature, and thermal stability and also greatly decreased elongation and shrinkage. The average molecular weight between crosslinks was calculated. The effect of crosslinking amorphous fibers and films was shown experimentally to produce materials with properties predicted for more rigid polymer structures.
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    Journal of Applied Polymer Science 2 (1959), S. 252-253 
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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 2 (1959), S. 256-256 
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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 2 (1959), S. 255-255 
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    Keywords: Chemistry ; Polymer and Materials Science
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    Journal of Applied Polymer Science 2 (1959), S. 273-280 
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    Notes: A method for determining molecular weight distributions is presented, based upon the partition of polymer molecules between gel and sol in a partly crosslinked system. It is assumed that the polymer sample consists of a series of molecular weight species, and analysis of previously developed theories covering this situation yields an expression which equates the weight fraction of gel to a summation involving the weight fraction of the material in each species and the number of crosslinked units in the sample. The data are presented in the form of a graph showing how the weight fraction of gel varies as a function of the number of crosslinked units in the sample. Data for the graph are obtained from swelling measurements made in the usual manner. The procedure is outlined for using the information from the graph to make a step-by-step evaluation of the fractional weight of each molecular weight species in the sample for as many fractions as may be arbitrarily chosen. Both a first approximation method and a more refined second approximation method are outlined. The procedure has been applied to samples of natural rubber, synthetic rubbers, and to two known molecular weight distributions.
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    Journal of Applied Polymer Science 2 (1959), S. 289-296 
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    Notes: The machanical anisotropy of several thermoplastic polymers has been investigated, and the relationship with a practical dart drop impact measurement has been explored. It has been shown that the unnotched Izod impact strength of a specimen taken perpendicular to flow orientation can be correlated with the dart drop impact strength. Further, the effect of several dart drop test variables, such as drop height, dart tip radius, and specimen size, have been investigated and reported. It has been concluded that the conventional strength measurement of injection-molded specimens may lead to erroneous appraisal of the practical strength of a material. Testing at an orientation normal to flow or by multiaxial stressing as in a dart drop test is suggested.
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    Journal of Applied Polymer Science 2 (1959), S. 308-311 
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    Notes: It was reported in Part I of this series that coatings of various polymers containing cinnamic ester groups are rendered insoluble by exposure to ultraviolet radiation, and that the rate of insolubilization may be increased by the inclusion of certain organic compounds. A continued systematic examination of the behavior of several hundred organic compounds has revealed that the ability to sensitize to some degree is quite general, provided that no complicating factors are present. The sensitivity of poly(vinyl cinnamate) is decreased by the presence of reducing groups in the addend, and sensitizing activity is lowered by interaction between adjacent groups. It is enhanced by the introduction of increasing conjugation and of ketone, nitro, or amino groups. Spectrograms of polymer-sensitizer combinations indicate that, with increasing sensitivity value, the sensitivity shifts towards, and, in some cases, into, the visible portion of the spectrum.
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    Notes: A technique is described for the small scale evaluation of plastisol formulations for molding, casting, coating, and foam applications. The technique described rapidly measures and automatically records the viscosity of a plastisol as a function of temperature by means of a Bendix Ultra-Viscoson and thermocouple. The measurements are made under conditions that closely approach process conditions. Small changes are accurately followed and the portion of the curve in the vicinity of gelation is amplified. The shape and position of the viscosity-temperature plot are dependent on the chemical nature of the plasticizer as well as the intrinsic viscosity and molecular weight distribution of the dispersed polymer. The resulting curves can be used to choose plastisol compositions for a given application. The application of the curves to foam and rotational casting formulations is outlined.
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    Journal of Applied Polymer Science 2 (1959), S. 328-332 
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    Notes: The effect of antirads (compounds added to reduce changes of polymer properties during irradiation) on the crosslink yields in black-loaded natural rubber stocks during gamma irradiation has been measured. The crosslink yields were determined by swelling techniques. Antirads decrease the crosslink yields if oxygen is absent. Oxygen alone effectively decreases crosslink yields. In the presence of oxygen some antirads further decrease crosslink yields, while others increase crosslink yields by their presence. These results may be explained in terms of competitive reactions between R. radicals, the antirad, and oxygen. Evaluation of the ratios of crosslink yields and scission yields indicate that most of the scission is temporary in nature, the chain breaks being reformed rapidly.
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    Journal of Applied Polymer Science 2 (1959), S. 333-336 
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    Notes: A vibrating reed apparatus for the measurement of dynamic Young's modulus has been constructed. The apparatus utilizes (a) a sensitive capacitance pick-up to measure displacement of a reed having approximately 0.001 g. of silver painted on the free end of the reed, (b) a clamp assembly which permits placement of the specimen in small temperature-controlled chambers, and (c) a linear variable differential transformer to facilitate maintenance of constant amplitude (independent of frequency) of the clamped end of the reed.
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    Journal of Applied Polymer Science 2 (1959), S. 351-353 
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    Notes: A new method is suggested for estimating the degree of isotacticity and the distribution of block lengths in semicrystalline polymers. The method is based upon the maximum attainable crystallinity and its dependence upon temperature. An alternate approach is based upon the dynamic shear modulus and its temperature dependence above the glass temperature.
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    Notes: Four antioxidant classifications, based on differences in the method by which they exert their effect, are noted. The mechanism of the chain-stopping action is discussed in terms of four different reactions which have been proposed. The participation of the antioxidant in the mechanism of inhibited thermal oxidation is reviewed. The hydrogen donation mechanism as the first step in the chain-stopping mechanism has been investigated by observing the effect of replacing the active hydrogen of the antioxidant by deuterium. Contrary to the findings of some prior workers, a kinetic isotope effect has been demonstrated with a secondary aryl amine antioxidant as well as with phenols. These results, together with other supporting evidences reported in the literature, indicate that abstraction of a hydrogen from the antioxidant is the initial step in the usual mechanism by which antioxidants serve as chain stoppers in the oxidation of hydrocarbon systems.
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    Journal of Applied Polymer Science 2 (1959), S. 358-362 
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    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Polystyrene has been partially or completely modified to contain varying amounts of vinyl-trans-benzalacetophenone units in the polymer chain. Acetylation of polystyrene gave a pure poly(vinylacetophenone) which, when condensed with benzaldehyde, produced varying proportions of vinyl-trans-benzalacetophenone in the polymer. These styryl ketone polymers are very sensitive to ultraviolet radiation, thin layers becoming insoluble on brief exposure, yet can be stored in the dark for years without change.
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    Journal of Applied Polymer Science 2 (1959), S. 363-366 
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    Notes: Five different types of polyethylene were irradiated in air and their melt indices determined as a function of the radiation dose. A resonant transformer electron beam generator was the source of radiation, and cellophane dye dosimetry was used to determine the radiation dose. The melt index was found to change uniformly with dose, and a single empirical equation was derived which describes the curves for all five types of polyethylene. By using the melt index as a measure of crosslinking, it was shown that the effect of radiation intensity on crosslinking is negligible.
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    Journal of Applied Polymer Science 2 (1959), S. 373-373 
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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 1 (1959), S. 1-1 
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    Keywords: Chemistry ; Polymer and Materials Science
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    Notes: Vinyl chloride monomer was polymerized in an emulsion system in the presence of a redox catalyst and relatively low concentrations of emulsifier. The effects of sodium bisulfite, potassium persulfate, and commercial sodium lauryl sulfate concentrations on particle initiation were determined by response-surface experimentation. A regression equation was developed which describes the number of particles per unit volume initiated in this vinyl chloride emulsion system. At subcritical emulsifier concentrations, the number of particles initiated was dependent primarily upon the emulsifier and sodium bisulfite concentrations and to a lesser degree upon the persulfate concentration. As the critical micelle concentration was approached, an apparent change in the particle initiation mechanism was observed, in that the sodium bisulfite concentration ceased to have an effect. In this system the change occurred at a concentration of 0.005% emulsifier.
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    Journal of Applied Polymer Science 1 (1959), S. 28-36 
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    Notes: The force as a function of temperature at constant length for cellulose model filaments swollen in water shows a maximum the temperature of which decreases with increasing orientation. At an orientation achieved by a prestretch of 80%, no more maximum exists, and the force decreases monotonically with increasing temperature. This behavior cannot be attributed to changes in the entropy and enthalpy of elongation with temperature, but is due rather to changes in the degree of swelling. When corrections are made for this, the positive force-temperature coefficient observed for some of the curves becomes negative. The equilibrium stress-strain curves are linear up to elongations of 5%. The-oretical evaluation of these curves is not possible with the present state of theory. Filaments with predominantly a skin structure show a minimum in the force-temperature curves; this is the more common behavior.
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    Journal of Applied Polymer Science 1 (1959), S. 50-55 
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    Notes: A new method for preparing plastic membranes with very small pores is described. The method involves dissolving two or more film-forming polymers in a common solvent. A thin layer of the resulting solution is spread on a smooth surface and the solvent is allowed to evaporate. One of the polymers is then extracted from the resulting film with a selective solvent. The selective permeability of ethyl cellulose was altered considerably using polyethylene glycol as the second polymer. The apparatus for determining the permeability of these films is described. Pictures of the membranes at different stages in their preparation are shown. Electron micrographs demonstrating the effect of this treatment on ethyl cellulose are presented.
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    Journal of Applied Polymer Science 1 (1959), S. 70-72 
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The ultraviolet spectra of aqueous solutions of polyvinyl alcohol have been examined with a view to identifying the chromophores present. The spectrum may be modified by reduction with hydrogen over Raney nickel at room temperature, which is specific for ethylenic unsaturation, and by reduction with sodium borohydride, which is specific for carbonyl groups. An analysis of the resulting spectra supports the proposal that the ultraviolet absorption of aqueous polyvinyl alcohol solutions arises from polyene-carbonyl chromophores of empirical formulas: —(CH=CH)n—CO—, where n may vary from 0 to 3.
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  • 82
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    Journal of Applied Polymer Science 1 (1959), S. 73-83 
    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: Twenty-two α-olefin monomers with varying degrees and types of branching in the lateral group have been polymerized and the polymers characterized. In general, the closer the branching in the side chain is to the polyethylene trunk, the higher the degree of crystallinity and the crystalline melting point. The degree of branching and the symmetry of the branches also affects the melting point and crystallinity markedly. Relationships have been drawn between type and position of the branch and melting point.
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  • 83
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    Journal of Applied Polymer Science 1 (1959), S. 84-90 
    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 aging of sulfurless tetraalkylthiuramdisulfide vulcanizates has been studied by the stress-relaxation technique, the general behavior being independent of the nature of the alkyl group. The aging in air at 100°C. of fully cured vulcanizates is excellent before acetone extraction but rapid after it, due to removal of zine dialkyldithiocarbamates which are powerful antioxidants. In undercured vulcanizates, the network breakdown at 100°C. after extraction is much less than in fully cured samples, and there is considerable crosslinking during the aging. This behavior is attributed to the presence of a vulcanization intermediate which, at 100°C., brings about crosslinking with formation of zine dialkyldithiocarbamate and which cannot be removed by acetone extraction. The presence of such an intermediate is confirmed by the ability of extracted undercured thiuram vulcanizates to be further crosslinked in the press at 140°C. Previous theories regarding thiuram vulcanization are discussed in the light of these observations. The rapid initial relaxation of unextracted undercured vulcanizates may be due to the breakdown of this vulcanization intermediate. During the thermal aging of apparently fully cured samples, some crosslinking occurs which is considered to be due to a direct oxidative reaction of dithiocarbamates. Unextracted thiuram vulcanizates degrade very little on illumination with ultraviolet light (wavelength 365 mμ), but, after extraction, the photolytic aging becomes more rapid. There is no variation in the rate of this type of aging with degree of cure, presumably because the vulcanization intermediate is light stable.
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  • 84
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    Journal of Applied Polymer Science 1 (1959), S. 121-126 
    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: Transitions in polymers have been studied with the use of a differential expansion apparatus modified from a design described by K. L. Floyd. Materials ranging from uncured, soft rubbers to hard, waxy solids have been studied from above room temperature down to liquid air temperatures. Both the first-order transition temperature, Tm and the second-order transition temperature, Tg, can be identified. Multiple changes in slope of the expansion curves indicate the possibility of additional second-order transitions. Expansion curves for several diene rubbers are presented, illustrating typical transition phenomena. Expansion curves for several polyolefin materials are presented which illustrate changes in Tg and in the low temperature expansion coefficient with changes in the structure of the polymer.
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  • 85
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    Journal of Applied Polymer Science 1 (1959), S. 127-127 
    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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  • 86
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    Journal of Applied Polymer Science 1 (1959), S. 150-157 
    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 dynamic mechanical properties at small strains have been determined for Hypalon-20 synthetic rubber, a commerical elastomer, by means of an electromagnetic transducer which is a modification of one described by Marvin, Fitzgerald, and Ferry. The measurements cover frequencies from 25 to 2500 cycles/sec. at twelve temperatures ranging from -8.4 to 68.4°C. Values of the real portion of the shear modulus (G′) vary from 7 × 106 to 2.1 × 109 dynes/cm.2, and those of the imaginary portion (G″) from 2.1 × 106 to 9 × 108 dynes/cm.2. The method of reduced variables (i.e., temperature-frequency superposition) is applicable and is used to extend G′ and G″ over the range 10-1 to 109 radians/sec. At 25°C., G″/G′ = 1.3 at its maximum at 105 radians/sec. The general function for the temperature dependence of mechanical properties proposed by Williams, Landel, and Ferry is valid up to 35°C. if one uses -24.5°C. for the glass transition temperature (Tg); dilatometrically Tg = -28 ± 1°C. The distribution function of relaxation times H(τ) has a pronounced maximum at about τ = 10-8 sec., decreases with a slope of about -0.57 (for log H versus log τ) to about τ = 10-3 sec., and is nearly flat from τ = 10-2 to 10 sec. H (τ) for Hypalon-20 is similar to those for polyisobutylene and polyhexene-1.
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  • 87
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    Journal of Applied Polymer Science 1 (1959), S. 144-149 
    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: Linear viscoelastic bodies satisfy the Boltzmann superposition principle which permits the calculation of the effect of arbitrary stress or strain history in terms of creep or stress relaxation parameters, respectively. In such calculations, the temperature is not considered as an independent variable; rather, the temperature must be constant, and the stress relaxation and creep parameters used are for the given temperature. By assuming the validity of the time-temperature superposition principle, it is shown how an arbitrary thermal history may be included. By employing spring-dashpot model methods, Boltzmann's principle is generalized, leading to the concepts of equivalent stress σ(t) and equivalent time w(t), the latter concept having also been introduced for creep and stress relaxation by Hopkins. These quantities are defined by \documentclass{article}\pagestyle{empty}\begin{document}$\sigma(t)=\rho(0)T(0)S(t)/\rho(t)T(t),w(t)=\int_0^t dt^{\prime}/a[T(t^{\prime}),T(0)]$\end{document} where t = time, p = density, T = temperature, and a[T(t), T(0)] is the time-temperature shift factor between temperatures T(0) and T(t). In terms of the equivalent stress and equivalent time, Boltzmann's principle for shear remains the same as for the isothermal case with stress relaxation or creep parameters at the initial temperature, T(0). In the case of tensile experiments, the observed strain must be corrected for thermal expansion.
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  • 88
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    Journal of Applied Polymer Science 1 (1959), S. 164-168 
    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: Stable, high molecular weight polymers of formaldehyde have been studied to determine their molecular structure. The polymer chain was shown to be a polyoxymethylene by chemical analysis and infrared absorption spectra. Infrared techniques also revealed hydroxyl end groups which were replaced by acetate groups on esterification. The endgroups, which were also measured by chemical methods, were used to determine the number-average molecular weight over the range 20,000 to 98,000. Values obtained by assuming two endgroups per molecule agreed with osmotic pressure results, thus showing this to be an essentially unbranched polymer. Two theoretically possible branch-point structures were investigated by chemical methods; none could be detected, further indicating a linear polymer structure. Indirect evidence of narrow molecular weight distribution was obtained by comparing melt viscosity properties with those of other polymers of known wide and narrow distribution.
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  • 89
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    Journal of Applied Polymer Science 1 (1959), S. 63-69 
    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: Measurements of the (complex) dynamic Young's modulus of natural rubber have been made by a wave propagation technique on filaments held at mean extensions up to 600%. It is shown that the real and imaginary parts vary with strain in the same way as the equilibrium modulus obtained from “static” stress-strain measurements, the behavior up to about 140% extension being derivable from a Mooney-type stored-energy function and at higher strains being dominated increasingly by the effects of finite extensibility in the network. The viscoelastic behavior in the region up to 140% strain may then be characterized by four parameters, of which one vanishes and another is constant for the rubber studied. It is shown how these parameters may be used to derive the strain-dependence of the damping or loss-factor (tan δ) in this region. The effect of increasing extension upon the relaxation spectra, over the range 100 to 600% extension, is to displace the whole spectrum progressively to longer times.
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  • 90
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    Journal of Applied Polymer Science 1 (1959), S. 91-100 
    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 discussion of the methods for studying orientation of crystalline and amorphous regions in polyethylene films is given. Extruded polyethylene films and films after having been stretched approximately 200% were studied by the methods of x-ray diffraction and absorption of polarized infrared radiation. It is shown that in extruded polyethylene films the a-axes of the crystallites are oriented parallel to the extrusion direction. The amorphous regions in these are either not oriented or show only to a slight degree the orientation of chains perpendicular to the extrusion direction. When the polyethylene films are stretched, both the crystallites and the amorphous regions become oriented. In stretched films, the orientation of the crystallites is with c-axis parallel to the stretching direction, and the chains in the amorphous regions are also oriented parallel to the stretching direction. Two mechanisms by which a-axis orientation may arise during extrusion of polyethylene films, and a convenient method for determining the relative degree of a-axis orientation in polyethylene films are given. The relative degrees of a-axis orientation as determined by x-ray diffraction and dichroism of absorption at 13.70 μ are compared for a number of film samples.
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  • 91
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    Journal of Applied Polymer Science 1 (1959), S. 101-106 
    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 on mastication of polymers brought into a rubbery state by incorporation of liquids or rise in temperature is accounted for by the mechanicochemical mechanism previously advanced to explain the degradation of rubbers. The dependence of the reaction on shear rate has been shown indirectly, as with rubbers, by the negative temperature coefficient of reaction, and also directly by variation of masticator rotor speed and design. A further new feature is the influence of the nature as well as concentration of plasticizer on the rate of degradation and a correlation with the softening of the polymer. A limiting molecular weight is reached on prolonged mastication from whatever initial molecular weight.
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  • 92
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: A new initiating system, named the Veroxathionite system, for the copolymerization of butadiene (75)-styrene (25) is described. At 0°C., with the recipe: butadiene, 75 parts; styrene, 25 parts; water, 180 parts; potassium myristate, 5 parts; potassium pyrophosphate, 1 part; sulfole mercaptan, 0.3 part; 0.66 mmole of phenylcyclohexane hydroperoxide, 0.001 M ferric versenate, and 0.1 part of sodium dithionite, conversions of 45, 87, and 100% were reached in 1, 2, and 3 hours, respectively. The rate can be varied within wide limits by changing the concentration of iron. With only 10-4 M ferric versenate and 0.06 part of dithionite, 71% conversion is attained in 12 hours. The amount of dithionite must be adjusted to the amount of hydroperoxide and, to a lesser extent, to the amount of iron. With much more than one mole of dithionite per mole of hydroperoxide, dead-stops occur at low conversion due to exhaustion of hydroperoxide. The rate is determined by the concentration of ferric versenate, and an excess of versene over ferric iron has no effect. The addition of potassium pyrophosphate yields a latex which is of normal fluidity and free of precoagulation up to 80% conversion. The effects of polymerization variables are described. With methanol as antifreeze, a recipe is described which yields 75% conversion in 8 hours at -20°C. The reaction mechanism is very involved. It is concluded that an induced reaction between hydroperoxide and dithionite is responsible for the low efficiency of the radicals produced in this recipe.
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  • 93
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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 presence of spherulites in nylon 66 increases the yield point and reduces the effects of variations in per cent crystallinity. Decreasing the size of the spherulites through increased nucleation results in a higher flexural modulus and yield point, a lower ultimate elongation, and a loss of ductility. These effects are markedly reduced by raising the temperature or water content. The effects of spherulite size in nylon and grain size in metals such as mild steel are compared.
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  • 94
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    Journal of Applied Polymer Science 1 (1959), S. 245-249 
    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 comparison between the viscosity-molecular weight relationships for natural rubber degraded in thin films at 130 and 140°C. and on cold and hot mastication indicates a greater similarity of distribution on degradation by the mastication treatments. The hot mastication process is further differentiated from ordinary thermal reactions by the dependence of rate of degradation on the rate of shear. It does, however, differ from cold mastication in being primarily an oxidative-scission reaction. No differences were detected in the properties of networks prepared from rubbers masticated at high or low temperatures to the same level of degradation.
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  • 95
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    Journal of Applied Polymer Science 1 (1959), S. 250-250 
    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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  • 96
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    Journal of Applied Polymer Science 1 (1959), S. 251-251 
    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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  • 97
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    Journal of Applied Polymer Science 1 (1959), S. 256-256 
    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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  • 98
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    Journal of Applied Polymer Science 1 (1959), S. 267-271 
    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 dynamic tensile modulus and energy loss have been measured for nylon 66 monofilaments at 9 and 60°C. over a wide humidity range in forced longitudinal vibration experiments. The frequency range covered was about 3 to 30 cycles/sec. (radian frequency 20 to 200 sec.-1). The results show dispersion of mechanical properties with change in humidity at both temperatures. At 60°C. a well-defined maximum in the energy loss was observed, similar to that obtained previously at 35°C., but occurring at a somewhat lower water content. If a maximum in the energy loss exists at 9°C. (it is not well-defined), it occurs very near 100% R.H. A time-humidity superposition procedure is discussed by means of which the individual curves of modulus against frequency for the various humidities can be combined into a single “master curve” of modulus against reduced frequency. The order of magnitude of the activation energy for the dissipation mechanism has been estimated at 60-80 keal./mole.
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  • 99
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    Journal of Applied Polymer Science 1 (1959), S. 283-295 
    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: Latex thickening - the process of increasing the viscosity of a polymer emulsion by addition of a water-soluble polymer  - has been studied by rheological measurements and by the examination of other colloidal properties. For the systems studied, which represent a range of polymers in both the dispersion and solution phases, the flow curves were represented over a wide range of shear rate by the equation, S = K(τ - τ0)2, where S is shear stress, τ is shear rate, and K and τ0 are constants, of which the latter is considered to be a yield stress. Aside from the generality of the mathematical function, the behavior of various latex-thickener pairs is extremely specific to the pair involved. Additional data on latex creaming and on the influence of the thickener and latex concentrations confirms the specificity. The available data indicate that latex thickening is not simply an enhancement of the viscosity of the aqueous phase by the thickener, but that in addition to this the ability of the thickener to flocculate or deflocculate the latex is an important part of the mechanism of thickening. These colloidal interactions change, often precipitously, with minor changes in the polymers, the latex emulsifier, and the concentrations of the components.
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  • 100
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    Journal of Applied Polymer Science 1 (1959), S. 296-299 
    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: Copolymers of styrene-methyl methacrylate were irradiated in vacuo with γ-rays; viscosity changes and gas yields (moles gas per mole methyl methacrylate in copolymer) for H2, CO, CO2, CH4, HCOOCH3, and CH3OH were examined at doses of 1.0 Mrep to 10.0 Mrep. It was found that styrene molecules protect the copolymer from degrading while decreasing the gas yields up to a styrene concentration of about 0.5 mole fraction; above this concentration, these radiation effects are independent of composition. When styrene-methyl acrylate copolymers were irradiated, styrene offered protection aganist gelation but simultaneously increased the gas yields (gases liberated were identical with those from the first system).
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