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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 56 (1952), S. 693-696 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 55 (1951), S. 1474-1491 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 55 (1951), S. 325-336 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of chemical & engineering data 11 (1966), S. 89-91 
    ISSN: 1520-5134
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry 45 (1953), S. 2511-2517 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 1951-1962 
    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: Heterogeneous propionylation of cotton cellulose, in the form of yarn, was carried out by reaction with propionyl chloride, in a medium of pyridine and dimethylformamide (DMF). The product was a mixed propionate-α-propionylpropionate ester of DS varying from 0.24 to 2.94. The supramolecular structure of these esters was studied by kinetic analysis as well as by the measurements of density, refractive index, and x-ray diffraction. The Sakurada plot of DS against time of reaction showed a discontinuity at a DS of about 2.0, where the x-ray diffraction pattern shows almost complete loss of crystalline structure. The interpretation, based on the assumption that the Sakurada curve actually represents the sum of two simultaneous rate processes acting in the amorphous phase and at the crystalline surfaces, seems to explain the data adequately. The density showed a continuous decrease, consistent with the idea of continuous destruction of crystalline structure with progressive substitution. Refractive indices showed a continuous decrease with substitution and birefringence was almost absent at complete substitution. The calculated value of molar refraction for the sample of DS 2.94 agreed closely with the experimentally observed value. The x-ray diffraction intensity traces gave convincing evidence of the progressive decrystallization of cellulose with the degree of substitution. Decrystallization seems to be more or less complete at about a DS of 2.0.
    Additional Material: 5 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 11 (1967), S. 1683-1692 
    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 reaction of cotton cellulose fiber with propionyl chloride in pyridine-DMF medium, the degree of substitution based on weight gain was much higher than that based on saponification. Gas-liquid chromatograms of the pyrolysis products of the samples showed an extra peak. This was identified as 3-pentanone, which arises from the pyrolysis of α-propionylpropionic acid, a substance which was proposed by Malm and co-workers as a possible side product. This conclusion was further confirmed by the infrared and NMR spectra of the liquid, collected fractionally on pyrolysis of the sample. Quantitative GLC showed that one òut of every four hydroxyl groups is substituted with an α-propionylpropionyl moiety, the rest with propionyl groups. A possible mechanism for the side reaction has been proposed.
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 817-828 
    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 present paper describes the results of a preliminary study of certain physical and thermal properties of benzhydrylated cotton yarns. The 200-yd. lengths of 7/2 yarn consisting of purified mercerized cellulose were reacted in a special reactor to various degrees of substitution from DS 0.31 to DS 1.22 with benzhydryl bromide in a mixture of equal volumes of 2,6-lutidine and dimethylformamide. The products were examined for tensile strength at break, which decreased only slightly with substitution; ultimate elongation, which was relatively uniform at 60-70% of the control yarn; and tenacity, which decreased with substitution largely due to added weight. The energy of rupture remained relatively constant at about 50% above the control. Tensile stiffness decreased progressively with substitution to about 25% of the control. Density decreased 10-11% with substitution. Crystallinity of the cellulose largely disappeared with substitutions above DS 1, and the lattice of benzhydryl cellulose began to appear. Stiffness, elastic recovery and work recovery were measured on 5-in. specimens of the yarn in an oven while they were subjected to repeated extension to about 1-2% and relaxed as the temperature was raised twice to 200°C. and lowered. During the heating phase of the first cycle the yarn underwent considerable heat adaptation. However, during the cooling phase and during both heating and cooling phases of the second cycle, the yarns showed generally favorable behavior. Attempts are made to interpret the results in terms of molecular modifications.
    Additional Material: 7 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 1387-1407 
    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 heterogeneous cellulose reaction was studied by reacting cotton fiber in pyridine medium with propionyl chloride at different initial molar concentrations and at different temperatures. It has been observed that the kinetics of reaction does not follow Sakurada's diffusion equation closely, and the deviation is more noticeable at lower initial concentrations of the reagent and at lower temperatures. A non-uniform reaction rate is also evident from the time-substitution curve. The rate of substitution changes twice during the reaction, the latter change being associated with the loss of cellulose I crystal structure. In an attempt to treat the data according to simple chemical kinetics, the order has been found to decrease continuously from the beginning, suggesting thereby an autocatalytic type of behavior. However, at the finàl stages of the reaction, when the cellulose I structure was completely lost, the reaction behaved as a pseudo first-order type. The x-ray diffractograms of the reacted samples indicate that cellulose I crystallinity decreases from the beginning of the reaction and that a new crystalline lattice develops gradually. The formation of this new crystal lattice is hindered in the cellulose crystalline region due to the lack of freedom of the chains. The diffusion equation has been modified by substituting a crystallinity index for the rate of diffusion of solvent in a solvent-gel system and thus extending Sakurada's equation. A new mechanism has been proposed considering the simultaneous reactions in the amorphous and crystalline regions. This mechanism can explain the deviation of Sakurada's equation. The kinetics expressions are derived, based on the proposed mechanism. The kinetics of decrystallization of cellulose I is also presented. A satisfactory theoretical explanation is given for the fact that the fall of reaction rate occurs at the conclusion of decrystallization of the cellulose I structure.
    Additional Material: 7 Ill.
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