Chemical ionization mass spectrometry as a tool for studying the surface interactions of the air pollutant acetone with Degussa P25 TiO2

Catherine M. Schmidt*, Aditya Savara, Eric Weitz, Franz M Geiger

*Corresponding author for this work

Research output: Chapter in Book/Report/Conference proceedingConference contribution

Abstract

Indoor air pollution is an emerging problem in atmospheric chemistry. We have applied chemical ionization mass spectrometry (CIMS) to study the interaction of the indoor air pollutant acetone with Degussa P25 TiO2, a possible remediation catalyst. Acetone partial pressures representative of those commonly found in both indoor and outdoor environments (10-7 to 10-4 Torr) are used. This partial pressure range is critical because the nonlinear relationship between gas phase concentration and surface coverage makes the extrapolation of high partial pressure data to environmentally relevant conditions challenging. Experiments carried out at 298 K allow for the deconvolution of non-reactive and reactive binding processes. Equilibrium and dynamic isotherm experiments yield a sticking coefficient of approximately 1 × 10-4 that is independent of acetone partial pressures in the low partial pressure regime examined here. The room temperature equilibrium binding constant and the adsorption free energy are also reported. Additional experiments carried out between 300 and 400 K are used to determine enthalpies and entropies of adsorption and to discuss the applicability of different adsorption models.

Original languageEnglish (US)
Title of host publication233rd ACS National Meeting, Abstracts of Scientific Papers
StatePublished - Dec 28 2007
Event233rd ACS National Meeting - Chicago, IL, United States
Duration: Mar 25 2007Mar 29 2007

Other

Other233rd ACS National Meeting
Country/TerritoryUnited States
CityChicago, IL
Period3/25/073/29/07

ASJC Scopus subject areas

  • General Chemistry

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