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  • Polymer and Materials Science  (47)
  • Physics
  • 1980-1984
  • 1960-1964  (47)
  • 1961  (47)
Collection
Publisher
Years
  • 1980-1984
  • 1960-1964  (47)
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 527-533 
    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 system is described for automatic collection of stress-strain data for polymeric films on magnetic tape for subsequent automatic data reduction and computation of a variety of stress-strain parameters. Two shaft analog-to-digital encoders attached to a conventional tensile tester feed digital information to an incremental pulse recorder which stores all stress and strain data in two channels on 0.625-in. magnetic tape. Specimen information and test constants are inserted by the operator through a keyboard located at the tensile tester. The tape is subsequently fed into a standard digital computer through a special incremental pulse magnetic tape reader. The data pulses are internally stored and converted by means of a special program into eight significant stress-strain parameters for polymeric film samples, plus averages and standard deviations for groups of replicate determinations. These parameters include: corrected length of specimen, initial maximum tensile modulus, offset yield stress, strain at break, strain at maximum stress, maximum tensile stress, tensile stress at break, and work to break. While the program described applies to polymer film testing, both it and the digital recording equipment accessories are applicable with suitable modification, to any analog experimental data. Significant savings in man-hours and increased information output result from use of this system.
    Additional Material: 5 Ill.
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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: Investigations of the viscoelastic aspects of the mechanical behavior of polymers have been limited almost exclusively to relatively simple conditions of homogeneous stress, that is, to tension or shear loadings. In the present work a study has been made from the viscoelastic standpoint of the response of several elastomers to a much more complex type of stress distribution arising from penetration up to failure by a cylindrical indentor for a range of temperatures and rates of penetration. The failure or “puncture point” was determined by a dip in the recorded curve of load versus depth of penetration. The puncture strength values were reduced to 25°C. by applying the ratio of absolute temperatures and plotted against the logarithm of the reciprocal of the rate of penetration. These curves were then shifted on the time scale to give a master curve after the manner of Tobolsky and of Ferry. The logarithms of the shift factors thus obtained were related to the reciprocal of the absolute temperature over the range studied. The results indicate a broader generality for the viscoelastic principle of time-temperature equivalence than has usually been supposed.
    Additional Material: 13 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 49 (1961), S. 533-541 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The preparation of a completely isopropylated polystyrene by polymerization of p-isopropylstyrene monomer is described. This polymer was autoxidized in cyclohexane with lauroyl peroxide to give a material of good reproducibility and high purity. Methyl methacrylate was successfully grafted to the polymeric hydroperoxide by using a sugar-containing recipe. Homopolymer was separated from the graft copolymer by extraction. Evidence for grafting was obtained from solubility and fractionation behavior, as well as from light-scattering and viscosity measurements.
    Additional Material: 5 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 51 (1961), S. 527-539 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Through x-ray and infrared examinations of stereoregular polymers and copolymers of vinylaromatic monomers, the occurrence of chain isomorphism phenomena, together with many cases of a new type of isomorphism between monomeric units, have been proved. Isomorphism of macromolecules, allowing true solid solutions, has been observed when melting and crystallizing mixtures of homopolymers (i.e., isotactic polystyrene) and of crystalline copolymers (i.e., styrene-p-methylstyrene) having the same identity period and differing very little in lattice constants. Isomorphism among monomeric units occurs in copolymerizing monomers that have a chemical nature and shape slightly different one from the other, e.g., styrene and o-fluorostyrene. This allows the formation of crystallizable copolymers in the entire composition range. They show physical properties (lattice constants, melting temperatures, etc.) continuously varying between those of the pure homopolymers. The occurrence of isodimorphism phenomena has been observed in crystalline copolymers obtained from monomers the homopolymers of which have different crystalline structures (e.g., styrene-p-fluorostyrene), and also in copolymerizing styrene with monomers (e.g., p-methyl, p-chlorostyrene) giving only amorphous homopolymers. In the latter case, of course, the copolymers show crystallinity only in a limited composition range.
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 1-6 
    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: Investigations are being conducted on the factors involved in the breakup of Newtonian and non-Newtonian (viscoelastic) liquids in high velocity airstreams. Viscoelastic solutions are formed by the addition of small amounts of polymeric modifiers to the test liquid. The mechanism of breakup is shown to be significantly different between the thickened and unthickened solutions. It was found that Newtonian liquid drops are broken into very fine particles by a breakup mechanism which begins with a stripping of the liquid from the surface of the drop. On the other hand, drops of non-Newtonian liquids break up by formation of ligaments rather than by surface stripping and are broken into much larger particles. An increase in viscosity by a factor of 25 in the Newtonian liquids showed no significant change in the breakup mechanism.
    Additional Material: 10 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 354-363 
    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 elution method is essentially a single-stage process, whereas the thermal gradient method is a multistage process which depends upon a thermal gradient to bring about reprecipitation of polymer in the fractions. As a test of the effectiveness of the thermal gradient, comparisons have been made of fractionation by these two column methods on high molecular weight polystyrene samples. It was found that the thermal gradient method definitely provides superior resolution and reproducibility, as expected. However, the degree of fractionation obtained by the elution method was surprising, accounting for at least 80% of the sample under the usual conditions and giving complete fractionation with certain modifications of conditions. These results indicate the difference in performance of the two methods is less than expected from an elementary consideration of the operation of the columns, and fractionation by the elution method, as conducted here, exceeds that expected for a single-stage extraction process. Although the reasons for the observed behavior are not clear, the following conclusions have been reached about certain factors which influence fractionation. Alternative methods of controlling the concentration of polymer in the fractions give almost equivalent results but enhanced resolution of the high molecular weight portion of the sample is obtained with extended solvent gradients. The inhibitor, tert-butyl catechol, which it was necessary to add to the solvents to limit degradation of the very high molecular weight sample, plays a specific role in the fractionation due to a reaction with the polystyrene which alters the fractionation behavior without affecting the molecular weight. Also, trace amounts of chemical heterogeneity in the polymers, presumably hydroxyl groups, have a marked adverse effect on fractionation by the elution method and probably account for molecular weight reversals observed in some fractionations by the thermal gradient method. It is suggested that adsorption on the surface of the beads is responsiblp for the adverse effect of chemical heterogeneity on the fractionation and that possibly an adsorption which increases with molecular weight contributes to fractionation by the elution and thermal gradient methods.
    Additional Material: 4 Ill.
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  • 7
    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 cellulose of cotton yarns was reacted with acrylonitrile under conditions preventing their longitudinal contraction. Changes taking place in the fine structure of the fiber were studied by means of optical microscopy, density measurements, x-ray diffraction, and thermal stress behavior measurements. The results indicate that in spite of the strong tensions developed in the yarns, the reaction proceeds in both the accessible and the crystalline regions with considerable volume expansion and eventual disappearance of crystalline structure. Suggestions of a glass transition temperature appear at substitutions slightly above D.S. = 1. Annealing becomes possible at substitutions above D.S. = 2 with the development of the cyanoethyl cellulose crystal structure and over 40% increase in tensile strength. Changes in tenacity, ultimate elongation, energy of rupture, and immediate elastic recovery were also observed.
    Additional Material: 6 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 195-202 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The temperature dependence of the viscous component E2(1/T) of the dynamic modulus is reported for a homologous series of butadiene-styrene copolymers incorporated at various levels in styrene homopolymer. By the use of a vibrating reed technique based on resonance tuning, the frequency of the applied deformation was maintained essentially constant throughout the temperature range which included the glass transitions of the copolymers. It is shown that, when E2(1/T) for such mixed polymer systems is plotted against reciprocal absolute temperature, the area under the peak corresponding to a given copolymer affords a direct measure of the quantity of the copolymer present. Further, the temperature of maximum E2(1/T) is related to the mole fraction of bound styrene in the copolymer, and the shape of the peak is related to the statistical sequence lengths of styrene and butadiene in the copolymer.
    Additional Material: 5 Ill.
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  • 9
    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: Thermogravimetric data are generally more extensive than are comparable isothermal aging data, and therefore afford preliminary kinetic information in greater abundance. The kinetic analysis of the thermogram, by use of either its exact equation or a more convenient approximation formula, is straightforward in cases of volatilization via simple kinetics. Application of the analytical procedure to the thermogram for the zero-order volatilization of octamethylcyclotetrasiloxane yielded an estimate of 11.65 kcal./mole as the average heat of vaporization in the temperature range of 80 to 145°C. The apparent activation energy for the first-order pyrolytic volatilization of 200-mg. samples of pulverized polytetrafluoroethylene was estimated to be 66 to 68 kcal./mole in the temperature range of 520 to 610°C.
    Additional Material: 3 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 247-250 
    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
    Notes: A series of polymers have been prepared that contain ethyl, n-propyl, n-butyl, n-pentyl, and n-hexyl branches. We have determined the rocking vibrations of the branches and have shown that branches in solid polymers have their rocking vibrations at frequencies comparable with those shown by liquid hydrocarbons. The ethyl branches in seven different polymers have infrared absorption bands in the 785-760 cm. -1 (12.74-13.18 μ) region. The terminal n-propyl group absorbs at 740 cm.-1 (13.51 μ) and the n-propyl branch at 735 cm.-1 (13.61 μ). The n-butyl, n-pentyl, and n-hexyl branches in polymers have their infrared absorption at 724 cm.-1 (13.81 μ), 723 cm.-1 (13.83 μ) and 722 cm.-1 (13.85 μ), respectively. The above data have been used to identify ethyl, n-propyl, and n-butyl branches in polymers produced by the cationic polymerization of propylene and l-butene.
    Additional Material: 1 Ill.
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