Hybrid solgel double metal cyanide catalysts for the copolymerisation of styrene oxide and CO2This article was submitted following the 11th International Conference on Carbon Dioxide Utilization, June 2730, 2011 (Dijon-France).Electronic supplementary information (ESI) available. See DOI: 10.1039/c2gc16485j

Hybrid solgel catalysts of zinc hexacyanocobaltate and SiO 2 were prepared by co-precipitation of the double metal cyanide with silica. Hybrid catalysts prepared at moderately acidic conditions showed the best performance with respect to activity, selectivity and stability. The hybrid solgel materia...

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Hauptverfasser: Dienes, Yvonne, Leitner, Walter, Mller, Merlin G. J, Offermans, Willem K, Reier, Tobias, Reinholdt, Alexander, Weirich, Thomas E, Mller, Thomas E
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creator Dienes, Yvonne
Leitner, Walter
Mller, Merlin G. J
Offermans, Willem K
Reier, Tobias
Reinholdt, Alexander
Weirich, Thomas E
Mller, Thomas E
description Hybrid solgel catalysts of zinc hexacyanocobaltate and SiO 2 were prepared by co-precipitation of the double metal cyanide with silica. Hybrid catalysts prepared at moderately acidic conditions showed the best performance with respect to activity, selectivity and stability. The hybrid solgel materials displayed high catalytic activity for the copolymerisation of styrene oxide and carbon dioxide (up to 650 mol SO (mol Zn h) 1 ) and high productivity (575 g Polymer g Catalyst 1 ). They also displayed good selectivity to the polymeric product (8087%), while only little cyclic styrene carbonate was formed as side product. A detailed electron microscopy study of the hybrid solgel materials showed that the active phase consisted of thin platelets containing the metals in a molar ratio n Zn / n Co = 2.1, whereby the double metal cyanide was closely associated with silica. Hybrid solgel catalysts of zinc hexacyanocobaltate and SiO 2 were prepared by co-precipitation of the double metal cyanide with silica.
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title Hybrid solgel double metal cyanide catalysts for the copolymerisation of styrene oxide and CO2This article was submitted following the 11th International Conference on Carbon Dioxide Utilization, June 2730, 2011 (Dijon-France).Electronic supplementary information (ESI) available. See DOI: 10.1039/c2gc16485j
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