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Iwanowa, Xenia; Strunk, Jennifer; Löffler, Elke; Muhler, Martin; Merz, Klaus

Surface reaction of 2‐propanol on modified Keggin type polyoxometalates: In situ IR spectroscopic investigation of the surface acid–base properties

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  • Medientyp: E-Artikel
  • Titel: Surface reaction of 2‐propanol on modified Keggin type polyoxometalates: In situ IR spectroscopic investigation of the surface acid–base properties
  • Beteiligte: Iwanowa, Xenia; Strunk, Jennifer; Löffler, Elke; Muhler, Martin; Merz, Klaus
  • Erschienen: Wiley, 2013
  • Erschienen in: physica status solidi (b)
  • Sprache: Englisch
  • DOI: 10.1002/pssb.201248405
  • ISSN: 0370-1972; 1521-3951
  • Schlagwörter: Condensed Matter Physics ; Electronic, Optical and Magnetic Materials
  • Entstehung:
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  • Beschreibung: <jats:title>Abstract</jats:title><jats:p>In order to investigate the influence of modified Keggin‐polyoxometalates and supported gold particles on reactivity and reaction pathways in thermal 2‐propanol oxidation, titanium‐substituted, insoluble Cs<jats:sup>+</jats:sup>‐salts of the Keggin‐heteropolytungstate (H<jats:sub>3</jats:sub>PW<jats:sub>12</jats:sub>O<jats:sub>40</jats:sub>) Cs<jats:sub>3</jats:sub>PW<jats:sub>12</jats:sub>O<jats:sub>40</jats:sub> <jats:bold>1</jats:bold>, Cs<jats:sub>5</jats:sub>PW<jats:sub>11</jats:sub>TiO<jats:sub>40</jats:sub> · <jats:italic>n</jats:italic>H<jats:sub>2</jats:sub>O <jats:bold>2</jats:bold>, and supported gold composite Au/Cs<jats:sub>5</jats:sub>PW<jats:sub>11</jats:sub>TiO<jats:sub>40</jats:sub> · <jats:italic>n</jats:italic>H<jats:sub>2</jats:sub>O <jats:bold>3</jats:bold> were synthesized and characterized as molecular model catalysts. The Ti‐substituted polyoxometalate <jats:bold>2</jats:bold> did not show any observable activity in the gas phase oxidation of 2‐propanol. The presence of gold nano‐particles activates the supporting polyoxometalate <jats:bold>3</jats:bold> and enhances formation of different oxidation products (acetone, diisopropyl ether) depending on the presence of different types of active sites. The formation of the diisopropyl ether involves two adjacent 2‐propanol molecules adsorbed on two different types of active sites, whereas the dehydrogenation reaction for the acetone formation involves the initial adsorption of 2‐propanol on one type of active site.</jats:p>