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  • Polymer and Materials Science  (23)
  • INSTRUMENTATION AND PHOTOGRAPHY  (10)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 1 (1959), S. 254-254 
    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
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 1 (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
    Additional Material: 3 Tab.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 1 (1959), S. 329-335 
    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: 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.
    Additional Material: 7 Ill.
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  • 4
    ISSN: 1040-0397
    Keywords: Hydrogen peroxide ; Palladium ; Thin-film ; Electrocatalysis ; Sensors ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A thin-film composite metal electrode is described for the amperometric measurement of hydrogen peroxide. By thermally evaporating a 27 μM layer of gold/palladium through a copper mask onto a plastic substrate a number of chemically equivalent sensing elements can be prepared. On these electrodes, hydrogen peroxide can be oxidized at a voltage of 0.4V (SCE). A model for the oxidation of peroxide at these electrodes is described based upon reversible binding of hydrogen peroxide to electrochemically generated palladium oxide sites.
    Additional Material: 10 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 8 (1952), S. 445-445 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 33 (1958), S. 417-427 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The use of ultrafein filters as osmotic membranes has been investigated in various solvents. It has been found that, at 30°C., measurements can be made in benzene, toluene, ethanol, water, and, with difficulty, methyl ethyl ketone, but not in chloroform or dimethylformamide. In benzene it has been found that all grades of the membranes are more selective than the corresponding ultracella filters and that, with the allerfeinst grade, molecular weights of the order of 2000 can be determined. With solutions of pentaerythritol tetrastearate (M.W. 1200), tristearin (M.W. 891), and sucrose octaacetate (M.W. 679), the osmotic pressures developed were less than the theoretical values. The ratios of observed to theoretical osmotic pressure decreased with molecular weight, and these ratios appear to be examples of the reflection coefficients predicted by Staverman.
    Additional Material: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 37 (1959), S. 241-250 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Gamma- radiation induced graft copolymerization of methyl methacrylate with natural rubber is characterized by high yields of grafted polymer even at relatively high monomer concentrations. The rates are first order except at low monomer concentrations; above 95% rubber concentration the polymerization rates are very low. A reaction mechanism has heen proposed in which it is shown that these results are consistent with a relatively slow initiation step between rubber radicals and methyl methacrylate and a rapid crossed termination reaction between methacrylate radicals and rubber radicals. In order to explain the high yield of grafted polymer, it has been assumed that radicals produced from methyl methacrylate by gamma-radiation are, unlike the growing methacrylate chains, capable of attacking the rubber molecule and thus from sites for grafting to occur, and also that monomer transfer is negligeable.
    Additional Material: 4 Ill.
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  • 8
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Linear polybutadienes, prepared with butyllithium as catalyst, and polybutadienes branched by exposure to γ-radiation have been fractionated and the fractions examined by osmometry and light scattering. Turbidimetric second virial coefficients (A2τ) of mixed polymer fractions are virtually the same as those of the higher molecular weight components of the mixtures for most compositions. This is true both for mixtures of linear with linear and linear with branched polymer. The higher the molecular weight of the fraction, the greater the effect; the addition of 1% microgel to a linear polymer reduced A2τ by a factor of three. The presence of microgel or high molecular weight branched polymer has been shown to be responsible for the very high molecular weights previously reported for polybutadienes from light scattering measurements. It is conveniently removed by shaking the solutions with calcium sulfate. Second virial coefficients obtained either by light scattering or osmometry are, within the limits of experimental error, uninfluenced by branching in the polymer. In general those factors which lead to increased branching also result in increased polydispersity, and it is the latter which results in the decrease in A2τ. The fall of the osmotic second virial coefficient (A2τ) with molecular weight is much smaller than would be calculated theoretically, and the fall in A2τ is greater than would be expected, notwithstanding the fact that for some of the fractions M̄u/M̄n 〈 1.1. This indicates that A2π is sensitive to the low molecular weight species presented in the fractions, whereas the reverse must apply to A2τ. Natural of synthetic trans-polyisoprene showed analogous behavior to polybutadiene, although, owing to experimental difficulties, sharp branched fractions could not be obtained. The following viscosity-molecular weight relationships were obtained in benzene solution: [η] = 1.45 × 10-4M0.76 for butyllithium-catalyzed polybutadienes, and [η] = 4.37 × 10-4M0.65 for natural and synthetic trans-polyisoprenes.
    Additional Material: 12 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 34 (1959), S. 651-670 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Graft copolymers have been prepared from natural rubber latex and methyl methacrylate using visible, ultraviolet, and γ-radiation. The influence of monomer concentration, temperature, radiation intensity, and, in the case of photoinitiation, photosensitizer concentration, on polymerization rates and molecular weights have been studied. The proportion of graft polymer is very high initially but falls with conversion and with increase in monomer concentration. Photoinitiated grafting depends on the photosensitizer and on temperature, but with γ-initiation the fraction grafted is independent of temperature. In the latter case the high proportion of graft cannot be explained in terms ofthe relative G values and concentrations of monomer and rubber. The fall-off in proportion of graft with conversion is thought to result from microscopic heterogeneous regions formed during polymerization, which are believed to increase in size as polymerization proceeds, thereby reducing further the possibility of grafting. Degradation of previously grafted polymer by prolonged irradiation is not of consequence in this case. Molecular weights of grafted and ungrafted polymers are very similar, except at low monomer concentrations, and a marked feature of this system is their constancy with change in all reaction conditions other than monomer concentration. Estimates of the utilization of radiation energy have been made and it is concluded that on an energy basis γ and photoinitiated reactions are of comparable efficiency.
    Additional Material: 6 Ill.
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  • 10
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The CD spectra and melting profiles have been measured for nine synthetic double-stranded RNAs containing I · C instead of G · C base pairs: poly[r(I) · r(C)], poly[r(I-C) · r(I-C)], poly[r(A-I-C) · r(I-C-U)], poly[r(A-C) · r(I-U)], poly[r(A-I) · r(C-U)], poly[r(A-C-C) · r(I-I-U)], poly[r(A-A-C) · r(I-U-U)], poly[r(A-C-U) · r(A-I-U)], and poly[r(A-U-C) · r(I-A-U)]. CD spectra have not previously been reported for the latter six of these polymers. The substitution of inosinate for guanylate led to recognizable CD differences, with all but two of the polymers having two resolved positive bands above 230 nm. Also, the I-containing RNAs differed from their G-containing counterparts in the almost complete absence of negative CD bands at long wavelengths and in the reduction of negative CD bands near 210 nm. First-neighbor comparisons showed that the CD spectra of the I-containing RNAs were consistent with the nearest-neighbor sequences of the polymers, as previously shown for G-containing RNAs (D. M. Gray, J.-J. Liu, R. L. Ratliff, and F. S. Allen, Biopolymers (1981) 20, 1337-1382). Moreover, two of the first-neighbor comparisons involved spectra of poly[r(A) · r(U)] and poly[r(I) · r(C)], polymers known to be in the A family of conformations in fibers (S. Arnott, D. W. L. Hukins, S. D. Dover, W. Fuller, and A. Hodgson, (1973) J. Mol. Biol. 81, 107-122). Thus, differences in the CD spectra of I- and G-containing RNAs could be simply explained as resulting from differences in the hypoxanthine and guanine chromophores, without invoking differences in conformation. Finally, melting temperatures of the I-containing RNAs were found to vary much less with base composition than do the melting temperatures of G-containing RNAs, since A · U base pairs are closer to I · C than to G · C base pairs in stability.
    Additional Material: 5 Ill.
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