Complete oxidation of benzene in air over Pt/TiO2 photocatalysts

Hisahiro Einaga; Shigeru Futamura; Takashi Ibusuki

doi:10.1627/jpi1958.42.363

Complete oxidation of benzene in air over Pt/TiO₂ photocatalysts

Hisahiro Einaga, Shigeru Futamura, Takashi Ibusuki

Research output: Contribution to journal › Article › peer-review

2 Citations (Scopus)

Abstract

Photocatalytic oxidation of benzene in air oer Pt/TiO₂ photocatalysts was studied at room temperature (relative humidity 65%). The complete oxidation of benzene to CO₂ was achieved when 1.0 wt % Pt/TiO₂ was used as the catalyst. With the increase in the amount of Pt loaded on TiO₂, the selectivity of CO₂ was increased and that of CO was decreased without any change in the catalytic activity for the CO₂ formation.

Original language	English
Pages (from-to)	363-364
Number of pages	2
Journal	Sekiyu Gakkaishi (Journal of the Japan Petroleum Institute)
Volume	42
Issue number	5
DOIs	https://doi.org/10.1627/jpi1958.42.363
Publication status	Published - Sep 1999
Externally published	Yes

All Science Journal Classification (ASJC) codes

Fuel Technology
Energy Engineering and Power Technology

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abstract = "Photocatalytic oxidation of benzene in air oer Pt/TiO2 photocatalysts was studied at room temperature (relative humidity 65%). The complete oxidation of benzene to CO2 was achieved when 1.0 wt % Pt/TiO2 was used as the catalyst. With the increase in the amount of Pt loaded on TiO2, the selectivity of CO2 was increased and that of CO was decreased without any change in the catalytic activity for the CO2 formation.",

author = "Hisahiro Einaga and Shigeru Futamura and Takashi Ibusuki",

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AB - Photocatalytic oxidation of benzene in air oer Pt/TiO2 photocatalysts was studied at room temperature (relative humidity 65%). The complete oxidation of benzene to CO2 was achieved when 1.0 wt % Pt/TiO2 was used as the catalyst. With the increase in the amount of Pt loaded on TiO2, the selectivity of CO2 was increased and that of CO was decreased without any change in the catalytic activity for the CO2 formation.

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