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  • 1970-1974  (3)
  • 1955-1959
  • 1970  (3)
  • Chemistry  (3)
Material
Years
  • 1970-1974  (3)
  • 1955-1959
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 14 (1970), S. 2905-2920 
    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: Cotton fiber was treated with aqueous trimethylbenzylammonium hydroxide (Triton B) at concentrations over the range 25%-40%. After complete removal of the swelling agent, the samples were evaluated for the extent of swelling, strength and elongation, birefringence, moisture regain, density, crystallinity, x-ray diffraction patterns, and microfibrillar morphology. Electron-microscopical examination and other evaluation of fine structure properties revealed that the nature of swelling is intercrystalline up to 30% concentration of Triton B, and intracrystalline beyond that. Although the swelling as measured by propanol-2 retention after treatment with 30% Triton B is about twice as much as that of the control, the original structure remains almost unchanged except for some gain in strength and elongation and increase in moisture regain. At 32% Triton B concentration and beyond, rapid decrystallization takes place, accompanied by a fall in birefringence, density, and crystallinity index. X-Ray analysis showed significant loss of lateral order and partial conversion of cellulose I to cellulose II at 35% and 40% Triton B concentrations. The results indicate that, used at the critical concentration of 30%, Triton B can be a useful swelling agent for cotton fibers as it opens up the fine structure of cellulose considerably without impairing any important physical properties.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 2 (1970), S. 71-78 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Interpretation of the NMR spectra of the isomeric 2-cyano-2-alkyl-5-norbornenes allowed the assignment of their respective structures. In the case of the 2-cyano-2-methyl-5-norbornene the structure assignment was confirmed by chemical synthesis (alkaline hydrolysis and iodo-lactonisation).
    Notes: L'attribution de structure des deux isomères cyano-2 alcoyl-2 norbornène-5 est possible grǎce aux données de la RMN. Une interprétation des spectres de ces dérivés bicycliques set donnée. Dans le cas des cyano-2 méthyl-2 norbornènes-5 une confirmation de structure a pu ětre donnée par voie chimique (hydrolyse basique et iodolactonisation).
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 375 (1970), S. 202-208 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: In the B2O3—MO—MS (M = Mg, Mn, Fe, Co, Zn, Cd) systems six ternary phases have been isolated, four of them having the structure of the cubic variety of the boracite, Mg3B7O13Cl, and two the structure of the sodalite, Na4(SiAlO4)3Cl. Some properties of the new phases have been investigated.
    Notes: In den B2O3—MO—MS (M = Mg, Mn, Fe, Co, Zn, Cd)-Systemen wurden sechs neue Phasen isoliert und untersucht; vier haben die Struktur der kubischen Form des Borazit, Mg3B7O13Cl, und zwei die Struktur des Sodalit, Na4(SiAlO4)3Cl.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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