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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 5 (1959), S. 267-268 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: From time to time, A.I.Ch.E. Journal presents translations of certain technical articles written by our Japanese colleagues in their own language. These translations are made by Kenzi Etani, who received his B.S. in chemical engineering in 1953 at the Tokyo Institute of Technology and his M.S. in 1955 at M.I.T. He is associated with Stone & Webster and is an associate member of American Institute of Chemical Engineers. He is also a member of the Society of Chemical Engineers, Japan, and the Japan Oil Chemists' Society. His offer to help break down the language barrier is acknowledged.Abstracts, notation, literature cited, tables, and figure captions not published here appear in English in the original paper. No figure will be reproduced in these translations.The following article was published in Chemical Engineering (Japan), 21, pages 17-25 (1957).
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 15 (1955), S. 475-484 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In the solution polymerization of vinyl chloride with benzoyl peroxide, it was found that the initial rate of the polymerization was remarkably increased by adding dimethylaniline, but that conversion became constant at lower conversion. It was observed that when the rate became constant the benzoyl peroxide was completely decomposed and the reaction could be reinduced by adding more benzoyl peroxide. On the basis of these results, it seems possible that the polymerization is instituted by the benzoate radical and not by the dimethylaniline radical as suggested by Horner. The benzoate radical is produced through the reaction of dimethylaniline with benzoyl peroxide. In view of such considerations, we postulate a reaction mechanism for the polymerization of vinyl chloride.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 16 (1955), S. 92-93 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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