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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 19 (1975), S. 3361-3367 
    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: 2 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 23 (1977), S. 529-538 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Previous studies of copper-ion catalyzed ascorbic acid autoxidation have indicated zero-order, first-order, or Michaelis-Menten dependence of rate on ascorbic acid or copper concentrations and first- or half-order dependence on oxygen concentration. A simple mathematical model of gas-liquid mass transfer with liquid phase reaction accounts for the various behaviors. Use of an experimental technique that eliminates the mass transfer step shows that the oxidation rate dependence is first order in copper, half order in oxygen, and Michaelis-Menten in ascorbic acid concentrations.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 1015-1022 
    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 steady-state (d.c.) electrical conductivity of polypropylene has been measured as a function of temperature (25-150°C.) and field strength (0-94 kv./cm.). The temperature coefficient of the conductivity is 34.6 kcal./mole expressed as an activation energy. This is much larger than the activation energy for diffusion of small molecules in the same polymer. Thus, ionization rather than diffusion appears to be the primary activation process. The conductivity is nonohmic; the conductance quotient is a linear function of field strength but is larger than predicted by Onsager's theory. The ion “jump distance” as evaluated from the isothermal field dependence, is the same order of magnitude as the diffusional mean free path estimated from diffusion studies in other polymers. The conductivity, conduction activation energy, and field dependence appear to be relatively insensitive to polymer crystallinity.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 783-787 
    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: Monomers of vinyl formate, vinyl acetate, vinyl propionate, and vinyl butyrate were carefully purified by distillation in a Vigreux column and in a 56-plate glass helixpacked Todd column. The refractive indices and boiling points of the purified monomers agreed with those given in the literature. The purified samples were exposed to the radiation of a quartz mercury lamp in order to produce several per cent polymer. The refractive indices are tabulated and plotted in graphs.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 74 (1962), S. 60-68 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die kernmagnetische Resonanz des 31P-Kerns läßt sich für die Strukturaufklärung von Phosphor-Verbindungen sowie für analytische und kinetische Untersuchungen verwenden. Es wird ein Überblick über die bisher bestimmten 31P-Resonanzen gegeben.
    Additional Material: 6 Tab.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 44 (1960), S. 271-272 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A general procedure is described by means of which the kp/kt1/2 ratio can be determined for the graft polymerization of vinyl monomers in an organic substrate. The method takes rigorous account of the influence of monomer diffusion on the reaction kinetics. As an experimental example, the mutual radiation grafting of styrene onto ethyl cellulose film by use of 2-M.e.v. Van de Graaff electrons to initiate free radical formation is described in detail.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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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: The diffusion of styrene vapor in ethyl cellulose film has been studied as a function of styrene solubility in the film at 50°C. Methods and data are presented for determining the equilibrium solubility of styrene in ethyl cellulose as a function of vapor pressure at 50°C. The permeation rates of styrene vapor through 3-mil film were determined under steady state conditions for various pressures of pure styrene vapor on one side of the film and vacuum on the other side. From a plot of permeation rates versus styrene solubility the diffusion coefficient was calculated as a function of concentration. Measurements made over a concentration range of 0 to 0.7 g. styrene/cm.3 of unswollen film show that the diffusion coefficient first increases rapidly with concentration, then goes through a maximum, and finally levels off at 10-7 cm.2/sec. In the limited range of 0.06 to 0.10 g./cm.3 the diffusion coefficient varies exponentially with concentration as has been reported for other systems in a similar range. However, such a functionality does not represent the present system over a broad concentration range. These results, if generally applicable to other systems, indicate that the nature of the diffusion process for organic vapors in polymers may be considerably more complicated than formerly supposed.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It was established that phenol-2,4-disulfonyl chloride and α-naphthol-2, 4-disulfonyl chloride introduce new intramolecular or tertiary bonds into lysozyme. The phenolic hydroxyl group seems to make the cross linking reagents soluble in aqueous media; it was established that a sulfonylating; species does dissolve prior to hydrolysis but that the chlorosulfonyl groups are hydrolyzed within seconds of dissolution. New covalently linked residues were shown to be introduced by different, spectra. Peptide maps of the lysozyme treated with phenol-2,4-disulfonyl chloride. peroxidized, and digested with trypsin showed definite deletions and additions when compared with the control. Partial analysis of the peptides showed that cross linking between ε-amino groups of lysine residues had occurred. A certain degree of stabilization of lysozyme to inactivation by certain inactivating conditions was noted after treatment with the two reagents. Ultra-centrifugal analysis of the lysozyme treated with phenol-2,4-disulfonyl chloride showed that there was no detectable fraction having a higher molecular weight than native lysozyme. Tentative assignments of positions of cross linking were made.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 14 (1975), S. 173-196 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Miyazawa-Blout-Krimm (M-B-K) treatment of polypeptide absorption in the infrared is extended to the calculation of circular dichroism (CD), linear dichroism, and oriented CD for the amide I and amide II transitions. Matrix methods are applied to the α helix and β structures using measured values for the strengths and directions of the transition dipole moments and empirical values from M-B-K for the coupling constants.Relatively small aggregates, a 36-residue helix, and 8-chain × 4-residue β sheets, are large enough to show calculated absorption agreeing with M-B-K results, which are based on infinite lattices.In all cases the predicted CD is an approximately conservative couple. The strongest CD should appear in the α helix, Δε/ε ≃± 10-3 for both transitions. The amide II transition should show moderate CD couples in both β structures, Δε/ε ≃ (+2 to -1) × 10-4. The amide I transitions in β structures should show weak CD couples, Δε/ε = (+3 to -2) × 10-5, except that the negative branch in the antiparallel structure may be detectable (Δε/ε ≃ -2 × 10-4) because absorption is very low at its wavelength peak.CD on oriented samples should be enhanced over the unoriented cases, giving values as large as Δε/ε = 3 × 10-3 because particular directions of observation allow the light to avoid much of the absorption in the sample.If all three structures are considered as helices, then the larger distance of the transition dipoles from the axis in the α helix, and the orientations of the transitions in the different structures, are the factors that, in terms of our previous theoretical work [Snir and Schellman (1973) J. Phys. Chem. 77, 1653] satisfactorily explain the calculated results. Simple dipole-dipole interaction is calculated to make a substantial contribution to the coupling between groups.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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