Abstract

Photocatalytic oxidation of propane using hydrothermally synthesized TiO2 samples with similar primary crystal size containing different ratios of anatase, brookite and rutile phases has been studied by measuring light-induced propane conversion and in situ DRIFTS (diffuse reflectance Fourier transform infrared spectroscopy). Propane was found to adsorb on the photocatalysts, both in the absence and presence of light. The extent of adsorption depends on the phase composition of synthesized titania powders and, in general, it decreases with increasing rutile and brookite content. Still, the intrinsic activity for photocatalytic decomposition of propane is higher for photocatalysts with lower ability for propane adsorption, suggesting this is not the rate-limiting step. In situ DRIFTS analysis shows that bands related to adsorbed acetone, formate and bicarbonate species appear on the surface of the photocatalysts during illumination. Correlation of propane conversion and infrared (IR) data shows that the presence of formate and bicarbonate species, in excess with respect to acetone, is composition dependent, and results in relatively low activity of the respective TiO2. This study highlights the need for precise control of the phase composition to optimize rates in the photocatalytic oxidation of propane and a high rutile content seems to be favorable.

Highlights

  • IntroductionLight alkanes, are pollutants classified as VOCs (volatile organic compounds) that are mainly released to the atmosphere by the use of LPG (liquefied petroleum gases) and as constituents of automobile exhaust emissions [1]

  • Alkanes, and light alkanes, are pollutants classified as VOCs that are mainly released to the atmosphere by the use of LPG and as constituents of automobile exhaust emissions [1]

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Summary

Introduction

Light alkanes, are pollutants classified as VOCs (volatile organic compounds) that are mainly released to the atmosphere by the use of LPG (liquefied petroleum gases) and as constituents of automobile exhaust emissions [1]. Catalytic oxidation is one of the most useful techniques for the abatement of light alkanes. Limited research has been devoted to the photocatalytic oxidation of propane [5,6,7,8]. Finger et al, discuss the kinetics and mechanism of the photocatalytic oxidation of alkanes and alkenes with TiO2 photocatalysts. They indicate that a large electron supply is not sufficient

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