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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 12 (1979), S. 300-304 
    ISSN: 1520-5835
    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
    Macromolecules 12 (1979), S. 721-726 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    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 53 (1994), S. 763-768 
    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: Fraké, a tropical wood species from Cameroon, was reacted with 1% periodic acid solution at room temperature for 24 h. Untreated and treated woods were analyzed by ESCA. As expected, O1s and C2s were the predominant species in the spectra. While the O1s peak is featureless, the C1s peak can be decomposed into several components. These contributions were calculated, and it was observed that untreated and treated woods exhibit carbon atoms in classes C1 (carbon atoms bonded by a C—C or a C—H bond), C2 (carbon atoms bonded by a C—O bond), and C3 (carbon atoms bonded by a C=O or by a O—C—O bond). Class C4, which refers to carbon atoms bonded by O—C=O bonds, is completely absent. The periodic acid treatment produces a reduction in C1, an increase in C2, with C3 remaining relatively small. Accordingly, the expected oxidation of hydroxyl groups to carbonyl groups is not observed. It can be postulated that wood-periodic acid intermediates, which are believed to be cyclic periodic esters, do not decompose to form carbonyl groups but rather remain as stable complexes. © 1994 John Wiley & Sons, Inc.
    Additional Material: 3 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 19 (1975), S. 2609-2620 
    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 method has been developed which permits the quantitative determination of fiber orientation in a cellulosic sample (paper, nonwoven or composite). From the measured fibril angle distribution function and the observed variation in intensity of the (002) plane of the x-ray pattern, a parameter governing the fiber distribution function is obtained analytically. The method is demonstrated for two different paper samples showing a narrow and a large fiber orientation distribution. The method is rapid for a series of samples involving the same fibers and does not involve any operator interpretation. It gives directly the average fiber orientation function from the bulk of the sample, not just from its surface as microscopic methods do. It can be particularly useful in the analysis of paper-polymer laminates.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 857-867 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The viscoelastic properties of poly(α,α-diethyl-β-propiolactone) were investigated in the linear range using stress relaxation and dynamic mechanical methods. Using Ferry's reduction method, a horizontal shift factor was determined at each temperature, that satisfactorily agreed with the WLF equation in the transition zone. No vertical shift was required to superimpose different relaxation curves. The apparent activation energy was temperature dependent and passed through a maximum near Tg whose value is (311 ± 2)K. The relaxation spectrum has been calculated according to the first method of approximation of Schwarzl and Staverman. It consists of a high intensity plateau at shorter times, a wedge type portion with a slope of -0,15 and a low intensity plateau at longer times. Dynamical mechanical measurements revealed a β relaxation peak at 333 K and yielded the evidence of a γ peak around 120 K.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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