Identification of binding sites for acetaldehyde adsorption on titania nanorod surfaces using CIMS

© 2011 American Chemical Society

Bibliographische Detailangaben
Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1999. - 27(2011), 24 vom: 20. Dez., Seite 14842-8
1. Verfasser: Finkelstein-Shapiro, Daniel (VerfasserIn)
Weitere Verfasser: Buchbinder, Avram M, Vijayan, Baiju, Bhattacharyya, Kaustava, Weitz, Eric, Geiger, Franz M, Gray, Kimberly A
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2011
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Air Pollutants Formates Water 059QF0KO0R formic acid 0YIW783RG1 Carbon Dioxide mehr... 142M471B3J titanium dioxide 15FIX9V2JP Carbon Monoxide 7U1EE4V452 Titanium D1JT611TNE Acetaldehyde GO1N1ZPR3B Acetic Acid Q40Q9N063P Oxygen S88TT14065
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245 1 0 |a Identification of binding sites for acetaldehyde adsorption on titania nanorod surfaces using CIMS 
264 1 |c 2011 
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520 |a The interaction of acetaldehyde with TiO(2) nanorods has been studied under low pressures (acetaldehyde partial pressure range 10(-4)-10(-8) Torr) using chemical ionization mass spectrometry (CIMS). We quantitatively separate irreversible adsorption, reversible adsorption, and an uptake of acetaldehyde assigned to a thermally activated surface reaction. We find that, at room temperature and 1.2 Torr total pressure, 2.1 ± 0.4 molecules/nm(2) adsorb irreversibly, but this value exhibits a sharp decrease as the analyte partial pressure is lowered below 4 × 10(-4) Torr, regardless of exposure time. The number of reversible binding sites at saturation amounts to 0.09 ± 0.02 molecules/nm(2) with a free energy of adsorption of 43.8 ± 0.2 kJ/mol. We complement our measurements with FTIR spectroscopy and identify the thermal dark reaction as a combination of an aldol condensation and an oxidative adsorption that converts acetaldehyde to acetate or formate and CO, at a measured combined initial rate of 7 ± 1 × 10(-4) molecules/nm(2) s. By characterizing binding to different types of sites under dark conditions in the absence of oxygen and gas phase water, we set the stage to analyze site-specific photoefficiencies involved in the light-assisted mineralization of acetaldehyde to CO(2) 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 4 |a Research Support, U.S. Gov't, Non-P.H.S. 
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700 1 |a Buchbinder, Avram M  |e verfasserin  |4 aut 
700 1 |a Vijayan, Baiju  |e verfasserin  |4 aut 
700 1 |a Bhattacharyya, Kaustava  |e verfasserin  |4 aut 
700 1 |a Weitz, Eric  |e verfasserin  |4 aut 
700 1 |a Geiger, Franz M  |e verfasserin  |4 aut 
700 1 |a Gray, Kimberly A  |e verfasserin  |4 aut 
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