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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 19 (1993), S. 281-291 
    ISSN: 1572-879X
    Keywords: Benzyl alcohol reactions on zeolites ; anthracene, from benzyl alcohol ; stilbene, from benzyl alcohol ; benzyl alcohol, formation of anthracene from ; stilbene, formation of anthracene from ; zeolites, reaction of benzyl alcohol over
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The reaction of benzyl alcohol and dibenzyl ether on several zeolites was studied in the temperature range 300–500 °C. The major products were benzaldehyde and toluene due to disproportionation, anthracene due to intermolecular alkylation followed by cyclodehydration, benzyltoluenes due to alkylation followed by hydrogenolysis, and stilbene. The alkylation course was strongly influenced by shape selectivity with the large pore zeolites mainly yielding anthracene and the medium pore zeolites benzyltoluene. The formation of stilbene was a new observation which has a bearing on the mechanism of the methanol-to-hydrocarbon reactions.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Cellulose is conveniently functionalized to the corresponding S-benzoyl cellulose xanthate. Photolysis of S-benzoyl cellulose xanthate in presence of methyl methacrylate (MMA) initiated graft copolymerization which was confirmed by different analytical techniques.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 1069-1073 
    ISSN: 0887-624X
    Keywords: cardanol ; cardanyl acrylate ; self-crosslinkable polymer ; autooxidation ; hydroperoxide ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cardanyl acrylate (CA), a monomer that yields crosslinkable copolymers, was synthesized by the reaction of cardanol with acryloyl chloride. A linear polymer was obtained by solution polymerization of the monomer in toluene using 0.8% azobisisobutyronitrile as initiator. Upon removal of solvent, the polymer undergoes crosslinking on exposure to air (or UV light) to give an insoluble transparent film. However, in bulk and suspension polymerization the polymer undergoes in situ crosslinking in the absence of any crosslinking agent. The polymer was characterized by IR, NMR, DSC, and GPC. The crosslinking reaction of soluble polymer on exposure to air at ambient conditions was explained by the hydroperoxide theory. © 1993 John Wiley & Sons, Inc.
    Additional Material: 4 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 49 (1993), S. 2129-2135 
    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: Cardanol was functionalised to incorporate elements such as phosphorus and bromine and polymerised with formaldehyde or hexamethylenetetramine (HMTA) to get flame retardant polymers. Thus, monocardanyl phosphoric acid (MCPA), its bromoderivative (BrMCPA), and their formaldehyde condensates (MCPAF and BrMCPAF) and cross-linked polymers were prepared and characterized by IR, NMR, and GPC. Flammability and thermal stability of these polymers were evaluated by LOI and TGA, respectively, and compared with those of conventional cardanol-formaldehyde (CF) resin and its bromoderivative. TGA of MCPAF showed that although it is initially less stable than that of CF, its stability increases above 500°C over that of CF. Char yields of MCPAF and BrMCPAF are 21 and 27, respectively, and corresponding LOI values are 27 and 49. The present data do not support any synergism nor any additive effect between phosphorus and bromine, but a positive interaction between them is indicated with phosphorus mainly contributing in the condensed phase and bromine in the vapour phase mechanism. The activation energies in the range 20-30 kcal/mol for MCPAF suggest an ionic mechanism for its decomposition, whereas mainly a free radical type of decomposition is inferred for BrMCPAF with an activation energy in the range of 35-50 kcal/mol. © 1993 John Wiley & Sons, Inc.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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