Volume 210, Issue 1 pp. 281-289
Article

Heteropolyacids dispersed within a polymer matrix as a new catalytic systems with controlled oxidative-reductive and acid-base active centers

Wincenty Turek

Wincenty Turek

Silesia Universty of Technology, Department of Chemistry, Institute of Physical Chemistry and Technology of Polymers, ul. Strzody 9, 44 - 100 Gliwice, Poland

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Mieczyslaw Lapkowski

Mieczyslaw Lapkowski

Silesia Universty of Technology, Department of Chemistry, Institute of Physical Chemistry and Technology of Polymers, ul. Strzody 9, 44 - 100 Gliwice, Poland

Institute of Coal Chemistry, Polish Academy of Sciences, ul. Sowinskiego 5, 44 - 121 Gliwice, Poland

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Adam Pron

Adam Pron

Laboratoire de Physique des Metaux Synthetiques, UMR5819 (CEA-CNRS-Univ.J.Fourier-Grenoble), DRFMC, CEA-Grenoble, 17 Rue des Martyrs, 38054 Grenoble Cedex 9, France

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Joanna Debiec

Joanna Debiec

Silesia Universty of Technology, Department of Chemistry, Institute of Physical Chemistry and Technology of Polymers, ul. Strzody 9, 44 - 100 Gliwice, Poland

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Agnieszka Wolna

Agnieszka Wolna

Silesia Universty of Technology, Department of Chemistry, Institute of Physical Chemistry and Technology of Polymers, ul. Strzody 9, 44 - 100 Gliwice, Poland

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Wojciech Domagala

Wojciech Domagala

Silesia Universty of Technology, Department of Chemistry, Institute of Physical Chemistry and Technology of Polymers, ul. Strzody 9, 44 - 100 Gliwice, Poland

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First published: 04 May 2004
Citations: 2

Abstract

Polymer support such as polypyrrole was selected as a matrix for heteropolyacid H5PMo10V2O40 in an attempt to prepare heterogeneous catalysts containing two different active centers: protons and transition metal ions. Exchanging protons from heteropolyanions dispersed in polymer matrix into ferric or ferrous ions cause the modifications of their catalytic properties. It is manifested by decrease of activity of acid-base centers and increase of activity of oxidative-reductive centers. Oxidation state of iron in all samples before and after catalytic reaction is the same (Fe(III)), but their structure is not similar. For catalysts doped with ferric ions the structural order is much more pronounced than for these doped with ferrous ions.

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