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  • Chemistry  (6)
  • oxalic acid  (1)
  • 1955-1959  (7)
  • 1
    ISSN: 1573-5060
    Keywords: Brassica napus ; disease tolerance ; oxalic acid ; oxalate oxidase ; Sclerotinia sclerotiorum ; transformation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Oxalic acid is thought to have a primary role in the pathogenicity of several plant pathogens, notably Sclerotinia selerotiorum. A gene coding for the enzyme oxalate oxidase was isolated from barley roots and introduced into oilseed rape as a means of degrading oxalic acid in vivo. This report describes the production of several transgenic plants of oilseed rape and the characterisation of these plants by Southern, Western and enzyme activity assays. Plants were shown to contain an active oxalate oxidase enzyme and were tolerant of exogenously supplied oxalic acid.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 37 (1959), S. 313-315 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 19 (1956), S. 373-377 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A brief experimental investigation was made of the copolymerization of twelve alkoxysilanes with monochlorostyrene, vinyl chloride, and acrylonitrile. These new monomers include vinyltrimethoxy-, vinyltriethoxy-, vinyltriisoproxy-, vinylmethyldiethoxy-, vinylethyldiethoxy-, and vinylphenyldiethoxy-silanes as well as allyl-, propenyl-, 2-butenyl-, Δ3-cyclohexenyl-, 6-triethoxysilylbicyclo [2.2.1]heptane-2, and α-chlorovinyl-triethoxysilanes. No copolymerization took place with monochlorostyrene. In the copolymerizations with vinyl chloride, and with acrylonitrile, the reactivity ratio r2 was assumed to be zero and the value of r1 determined.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Studies have been made by a sorption-desorption procedure on the diffusion of water vapor at relative humidities of from 30 to 85% into the polymers, polyvinyl acetate cellulose acetate (37.9% acetyl), cellulose nitrate (12.0% N), 6-10 nylon, and polyvinyl alcohol. Diffusion of water in polyvinyl acetate obeys Fick's law at temperatures of from 30 to 50°C. and also at 22°C., which is below the second-order transition. The energy of activation for diffusion of water into polyvinyl acetate is 15 kcal. per mole and at 40°C. the diffusion coefficient is 7 × 10-6 cm.2/min. In contrast to the results with organic vapors, the diffusion coefficient for water is found to be independent of concentration of water in the polyvinyl acetate. Similar behavior is found for diffusion of water at 40° into cellulose acetate, cellulose nitrate, and 6-10 nylon. The chief difference is that for these three polymers the diffusion departs mildly from Fick's law at the later stages of some of the sorption and desorption experiments. This generally uncomplicated diffusion of water in these three polymers contrasts with the markedly anomalous diffusion found for organic vapors such as methanol and acetone into cellulose acetate and nitrate. With polyvinyl alcohol the diffusion of water is distinctly anomalous and closely resembles the non-Fickian diffusion of organic vapors in cellulose acetate and nitrate. One consequence is that the rate of sorption and desorption of water in polyvinyl alcohol is considerably slower than in the other polymers and is also concentration dependent.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Equilibrium and kinetic studies of the sorption and desorption of water vapor by poly(acrylic acid), poly(sodium acrylate), sodium carboxy methyl cellulose, methyl cellulose, and a series of poly(methyl acrylate) hydrolyzates in acid and sodium salt forms were made at 30°C. It was found, as expected, that equilibrium sorption increased and was greater for polymers containing strong-electrolyte type substituents than for those containing an equivalent number of weakly ionizable units. In general, the diffusion is somewhat slower than in the case of water-insoluble polymers. It was also found that water solubility of a polymer does not per se result in anomalous water sorption. In Methocel, for example, water diffusion is both Fickian and concentration-independent. All of the results, particularly those on the poly(methyl acrylate) hydrolyzates which ranged from completely water-soluble to insoluble systems, support the following conclusion: For water-soluble polymers both anomalous diffusion and relatively high glass temperatures are associated with high concentrations along polymer chains of very polar or ionic groups, such as —OH, —COOH, and CO2-Na+. Presumably both the anomalies and high transition temperatures are associated with restricted segmental mobility resulting from strong chain-chain interactions which originate in the highly polar and ionic, water-solubilizing chain substituents.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 41 (1959), S. 265-274 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: New data are presented to establish the Q and e values of vinylidene chloride, acrylonitrile, and vinyl chloride relative to styrene as the reference monomer. Within the experimental error these values are shown to be entirely consistent with the observed copolymer compositions. Only the values for vinyl chloride are appreciably different from those published in the original paper of Alfrey and Price in 1947. With these better data it is hoped that renewed efforts will be made to place this empirical device on a sound theoretical basis.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 34 (1959), S. 741-760 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Although crystallization under stress occurs in nearly all synthetic fiber making, giving fine fibrillar fiber structures, it has been relatively little studied; and the literature, centered mainly round coarser spherulitic crystallization, does not take us very far in understanding it. However, a simple experiment shows that it is very important. If a filament of amorphous polyethylene terephthalate is stretched over a hot plate between two roller moving at different speeds, stretching can take place either without crystalization at low tension, or with considerable crystallization at high tension, at the same temperature and speed, simply according to the method of starting the machine. A model visco-elastic theory based on Maxwell's equation is, therefore, developed to describe this behaviour using the simplest possible assumptions. Further experiments then show that this simple and partly empirical theory fits the observed behaviour of polyethylene terephthalate reasonably well, and the simple assumptions made, therefore, seem to give a first approximation to the course of strain induced crystallization. They correspond with the idea of exremely rapid crystallization from a nucleus to a small structural unit, the density of nucleation being dependent on the stress. Parallel work on the streching of spherulitic structures is then mentioned, and it is finally suggested that stress induction and rapid growth to a small structural unit may be common to both spherulitic crystallization under internal stresses, and fibrillar crystallization under an externally applied stress.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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