Impregnation of tungstophosphoric acid on poly(methacrylamide-co-methyl methacrylate) and its acid catalytic activity in TMB alkylation

Impregnation of tungstophosphoric acid on poly(methacrylamide-co-methyl methacrylate) and its... A poly(methacrylamide-co-methylmethacrylate) (abbreviated PMAA-MMA) polymer support was studied for supporting a heteropolyacid (tungstophosphoric acid, H3PW12O40) with its surface positively charged in the polymerization step. PMAA-MMA supports could be obtained in a porous form by eliminating template reagent molecules (benzylmalonic acid) combined with properly selected monomer (methacrylamide). The amount of amine groups in PMAA-MMA directly determined the amount of H3PW12O40 impregnated, because the amine groups induced a positive charge on the PMAA-MMA surface. Finally, H3PW12O40/PMAA-MMA showed better acid catalytic activities than unsupported H3PW12O40 in alkylation of 1,3,5-trimethylbenzene with cyclohexene, which confirmed that PMAA-MMA supported H3PW12O40 effectively. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Research on Chemical Intermediates Springer Journals

Impregnation of tungstophosphoric acid on poly(methacrylamide-co-methyl methacrylate) and its acid catalytic activity in TMB alkylation

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Publisher
Springer Netherlands
Copyright
Copyright © 2008 by Springer
Subject
Chemistry; Catalysis; Physical Chemistry; Inorganic Chemistry
ISSN
0922-6168
eISSN
1568-5675
D.O.I.
10.1007/BF03036943
Publisher site
See Article on Publisher Site

Abstract

A poly(methacrylamide-co-methylmethacrylate) (abbreviated PMAA-MMA) polymer support was studied for supporting a heteropolyacid (tungstophosphoric acid, H3PW12O40) with its surface positively charged in the polymerization step. PMAA-MMA supports could be obtained in a porous form by eliminating template reagent molecules (benzylmalonic acid) combined with properly selected monomer (methacrylamide). The amount of amine groups in PMAA-MMA directly determined the amount of H3PW12O40 impregnated, because the amine groups induced a positive charge on the PMAA-MMA surface. Finally, H3PW12O40/PMAA-MMA showed better acid catalytic activities than unsupported H3PW12O40 in alkylation of 1,3,5-trimethylbenzene with cyclohexene, which confirmed that PMAA-MMA supported H3PW12O40 effectively.

Journal

Research on Chemical IntermediatesSpringer Journals

Published: Apr 15, 2009

References

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