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  • 1
    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 addition of mercaptoethanol and hydrogen sulfide to the pendent double bonds of acrylamidomethylated cotton (AMC) has been investigated. The interaction of acrylonitrile with the modified celluloses so obtained (substrate I and II) and with AMC treated with ammonium hydroxide (substrate III) in the presence of Ce(IV) is studied. Substrate I shows higher initial grafting yields. than AMC; the opposite holds true for the maximum graft yields. The graft yields obtained with substrate II are lower than those of AMC. All modified cottons studied are less amenable to grafting compared with the unmodified cotton. The graft yields of AMC and substrate III are comparable due to the fact that both substrates are crosslinked. Probable reasons for the inferior reactivity of substrates I and II are also given.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 312 (1970), S. 737-743 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Both 5-aminobenzothiophene and 5-aminobenz-1,2,3-thiadiazole condense readily with 2,4-dinitrochlorobenzene to give dinitroanilino derivatives which provide after partial reduction the aminonitroanilino derivatives. Treatment of these o-diamines with the proper reagents affords triazole and imidazole derivatives. Oxidation of 4-arylazo-5-aminobenzothiophene or benz-1,2,3-thiadiazole yields the corresponding triazole derivatives.
    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 17 (1973), S. 2725-2738 
    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: Acrylamidomethylated cellulose (AMC) was prepared by reacting cellulose with N-methylolacrylamide or its ethers in acidic medium under a variety of conditions. The extent of the reaction, expressed as mmole double bonds per 1 g cellulose, increased by increasing the concentration of N-methylolacrylamide or its ethers. However, the paddry-cure technique produced AMC with greater amounts of double bonds than the pad-batch technique. Also, the reactivity of the etherifying agents follow the order N-methylolacrylamide〉N-methoxymethylacrylamide〉N-methoxymethylmethacrylamide. Furthermore, the behavior of AMC in neutral, alkaline, and acidic media was studied. No change in the amount of the pendent double bonds of AMC occurred in neutral medium regardless of the conditions employed. On the contrary, disappearance of the double bonds took place in alkaline medium. The extent of disappearance depends on the kind of alkali used as well as on the conditions implemented. It was disclosed that consumption of the pendent double bonds of AMC occurred mainly via addition of the cellulose hydroxyls to yield a crosslinked cellulose. Treatment with hydrochloric acid, on the other hand, resulted in partial splitting of the acrylamidomethyl groups as well as addition of the acid on the pendent double bonds of AMC.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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