Abstract

The effect of H2O and O2 on the adsorption and degradation of gaseous acetaldehyde on the anatase TiO2 surface has been studied, in the dark and upon UV illumination, at ambient temperatures. The processes occurring at the surface have been elucidated by means of in situ ATR–FTIR (Attenuated Total Reflection—Fourier Transform Infrared) spectroscopy, while gas detectors allowed the analysis of the adducts and products in the gas phase. In the dark and under dry conditions acetaldehyde reacts independently of the atmosphere, upon aldol condensation to crotonaldehyde. However, under humid conditions, this reaction was prevented due to the replacement of the adsorbed acetaldehyde molecules, by water molecules. Upon UV illumination under oxygenic conditions, acetaldehyde was decomposed to acetate and formate. Under an N2 atmosphere, the formation of acetate and formate was observed during the first hour of illumination, until all adsorbed oxygen had been consumed. In the absence of molecular oxygen acetate, methane, and CO2 were detected, the formation of which most likely involved the participation of the bridging O atoms, within the TiO2 lattice.

Highlights

  • Nowadays, the demand for clean and fresh indoor air is a public health issue

  • In situ ATR–FTIR (Attenuated Total Reflection–Fourier Transform Infrared) spectroscopy is an established technique that provides a deeper understanding of the interfacial processes occurring at the semiconductor/water interface

  • When a TiO2 film was treated with 1000 ppb gaseous

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Summary

Introduction

One major indoor air pollutant is acetaldehyde, which is a potential human carcinogen [1], whose maximum occupational exposure levels are set in Europe, and in the USA [2,3]. In situ ATR–FTIR (Attenuated Total Reflection–Fourier Transform Infrared) spectroscopy is an established technique that provides a deeper understanding of the interfacial processes occurring at the semiconductor/water interface. This technique allows the monitoring of the molecule adsorption from gaseous and from liquid phase on solid surfaces, as well as the detection of intermediates and products of photocatalytic processes [5,6]

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