Investigations into the direct synthesis of hydrogen peroxide and CO oxidation using precious metal catalysts

The direct synthesis of hydrogen peroxide from molecular hydrogen and oxygen represents an attractive atom efficient alternative to the current industrial auto-oxidation process which relies on the sequential oxidation and reduction of an anthraquinone. The first and most widely studied catalysts fo...

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Main Author: Freakley, Simon James
Published: Cardiff University 2012
Subjects:
547
Online Access:http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.569939
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spelling ndltd-bl.uk-oai-ethos.bl.uk-5699392015-11-03T03:35:21ZInvestigations into the direct synthesis of hydrogen peroxide and CO oxidation using precious metal catalystsFreakley, Simon James2012The direct synthesis of hydrogen peroxide from molecular hydrogen and oxygen represents an attractive atom efficient alternative to the current industrial auto-oxidation process which relies on the sequential oxidation and reduction of an anthraquinone. The first and most widely studied catalysts for this reaction were palladium based however over-hydrogenation of the synthesised hydrogen peroxide is a problem. Recent advances demonstrate that the addition of gold to the catalyst has been shown to significantly improve the productivity of the catalysts by suppressing the hydrogenation and decomposition activity. The work in this thesis shows that tin can be used as a catalyst additive as a direct replacement for gold by a simple impregnation method. By tuning the heat treatments of these bimetallic tin-palladium catalysts it was possible to switch off the competing hydrogenation and decomposition reactions. The construction of a small scale flow system has allowed the independent study of reaction variables and the determination of global kinetics and rate constants for the synthesis and subsequent reactions. It was shown that in a flow system it was the decomposition reaction that had a greater limiting effect on the production of hydrogen peroxide than the hydrogenation reaction. A study was also carried out into CO oxidation using gold / iron oxide catalyst prepared in Cardiff and by Prof. Haruta’s group in Tokyo. These catalysts underwent extensive tests to try and identify the active species of the catalyst. Detailed testing and STEM characterisation of the samples identified the possibility of different mechanisms operating at different temperatures and no correlation between the nanoparticle population and activity at sub ambient temperature could be made which challenges the hypothesis that nanoparticles are the most active species and that sub nanometer clusters may be the active species at low temperatures.547QD ChemistryCardiff Universityhttp://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.569939http://orca.cf.ac.uk/46829/Electronic Thesis or Dissertation
collection NDLTD
sources NDLTD
topic 547
QD Chemistry
spellingShingle 547
QD Chemistry
Freakley, Simon James
Investigations into the direct synthesis of hydrogen peroxide and CO oxidation using precious metal catalysts
description The direct synthesis of hydrogen peroxide from molecular hydrogen and oxygen represents an attractive atom efficient alternative to the current industrial auto-oxidation process which relies on the sequential oxidation and reduction of an anthraquinone. The first and most widely studied catalysts for this reaction were palladium based however over-hydrogenation of the synthesised hydrogen peroxide is a problem. Recent advances demonstrate that the addition of gold to the catalyst has been shown to significantly improve the productivity of the catalysts by suppressing the hydrogenation and decomposition activity. The work in this thesis shows that tin can be used as a catalyst additive as a direct replacement for gold by a simple impregnation method. By tuning the heat treatments of these bimetallic tin-palladium catalysts it was possible to switch off the competing hydrogenation and decomposition reactions. The construction of a small scale flow system has allowed the independent study of reaction variables and the determination of global kinetics and rate constants for the synthesis and subsequent reactions. It was shown that in a flow system it was the decomposition reaction that had a greater limiting effect on the production of hydrogen peroxide than the hydrogenation reaction. A study was also carried out into CO oxidation using gold / iron oxide catalyst prepared in Cardiff and by Prof. Haruta’s group in Tokyo. These catalysts underwent extensive tests to try and identify the active species of the catalyst. Detailed testing and STEM characterisation of the samples identified the possibility of different mechanisms operating at different temperatures and no correlation between the nanoparticle population and activity at sub ambient temperature could be made which challenges the hypothesis that nanoparticles are the most active species and that sub nanometer clusters may be the active species at low temperatures.
author Freakley, Simon James
author_facet Freakley, Simon James
author_sort Freakley, Simon James
title Investigations into the direct synthesis of hydrogen peroxide and CO oxidation using precious metal catalysts
title_short Investigations into the direct synthesis of hydrogen peroxide and CO oxidation using precious metal catalysts
title_full Investigations into the direct synthesis of hydrogen peroxide and CO oxidation using precious metal catalysts
title_fullStr Investigations into the direct synthesis of hydrogen peroxide and CO oxidation using precious metal catalysts
title_full_unstemmed Investigations into the direct synthesis of hydrogen peroxide and CO oxidation using precious metal catalysts
title_sort investigations into the direct synthesis of hydrogen peroxide and co oxidation using precious metal catalysts
publisher Cardiff University
publishDate 2012
url http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.569939
work_keys_str_mv AT freakleysimonjames investigationsintothedirectsynthesisofhydrogenperoxideandcooxidationusingpreciousmetalcatalysts
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