Quantitative analysis of superoxide ion and hydrogen peroxide produced from molecular oxygen on photoirradiated TiO2 particles

被引:301
作者
Goto, H [1 ]
Hanada, Y [1 ]
Ohno, T [1 ]
Matsumura, M [1 ]
机构
[1] Osaka Univ, Res Ctr Solar Energy Chem, Toyonaka, Osaka 5608531, Japan
关键词
titanium dioxide; photocatalyst; superoxide ion; hydrogen peroxide; anatase; rutile;
D O I
10.1016/j.jcat.2004.04.001
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The reduction of molecular oxygen is the counter reaction of most photocatalytic reactions proceeding oxidatively on titanium dioxide particles. We have quantitatively analyzed the reductive production of hydrogen peroxide and superoxide ion from oxygen in an aqueous solution containing 2-propanol as the scavenger of positive holes. The rates for the production of hydrogen peroxide and superoxide ion were determined by colorimetry using iodide and nitroblue tetrazolium, respectively. In addition, the oxidation of 2-propanol to acetone was monitored. Based on a comparison of these production rates, it was concluded that the main product from oxygen is hydrogen peroxide when TiO2 powder consisting mainly of anatase-form particles is used, whereas the main product is superoxide ion when TiO2 powder consisting mainly of rutile-form particles is used. The difference in the photocatalytic activity between these powders can be attributed to the difference between the reduction paths of oxygen on these powders. It was also found that the superoxide ion generated from molecular oxygen spontaneously reacts with 2-propanol to produce acetone and hydrogen peroxide. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:223 / 229
页数:7
相关论文
共 34 条
[11]   Influence of the electrolytes on electron transport in mesoporous TiO2-electrolyte systems [J].
Kambe, S ;
Nakade, S ;
Kitamura, T ;
Wada, Y ;
Yanagida, S .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (11) :2967-2972
[12]   ELECTROCHEMICAL CONVERSION OF CARBON-DIOXIDE TO METHANOL WITH THE ASSISTANCE OF FORMATE DEHYDROGENASE AND METHANOL DEHYDROGENASE AS BIOCATALYSTS [J].
KUWABATA, S ;
TSUDA, R ;
YONEYAMA, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (12) :5437-5443
[13]   Photocatalytic oxidation of dichloroacetic acid and dichloroacetyl chloride on TiO2:: active sites, effect of H2O, and reaction pathways [J].
Lukaski, AC ;
Muggli, DS .
CATALYSIS LETTERS, 2003, 89 (1-2) :129-138
[14]   PHOTOCHEMICAL MECHANISM OF SIZE-QUANTIZED VANADIUM-DOPED TIO2 PARTICLES [J].
MARTIN, ST ;
MORRISON, CL ;
HOFFMANN, MR .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (51) :13695-13704
[15]   PHOTOSENSITIZED DISSOCIATION OF WATER USING DISPERSED SUSPENSIONS OF N-TYPE SEMICONDUCTORS [J].
MILLS, A ;
PORTER, G .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1982, 78 :3659-3669
[16]   Autooxidation of acetaldehyde initiated by TiO2 photocatalysis under weak UV illumination [J].
Ohko, Y ;
Tryk, DA ;
Hashimoto, K ;
Fujishima, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 1998, 102 (15) :2699-2704
[17]   BLEACHING OF LIGNIN SOLUTION BY A PHOTOCATALYZED REACTION ON SEMICONDUCTOR PHOTOCATALYSTS [J].
OHNISHI, H ;
MATSUMURA, M ;
TSUBOMURA, H ;
IWASAKI, M .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1989, 28 (06) :719-724
[18]   TiO2-photocatalyzed oxidation of adamantane in solutions containing oxygen or hydrogen peroxide [J].
Ohno, T ;
Mitsui, T ;
Matsumura, M .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2003, 160 (1-2) :3-9
[19]   Unique effects of iron(III) ions on photocatalytic and photoelectrochemical properties of titanium dioxide [J].
Ohno, T ;
Haga, D ;
Fujihara, K ;
Kaizaki, K ;
Matsumura, M .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (33) :6415-6419
[20]   Synergism between rutile and anatase TiO2 particles in photocatalytic oxidation of naphthalene [J].
Ohno, T ;
Tokieda, K ;
Higashida, S ;
Matsumura, M .
APPLIED CATALYSIS A-GENERAL, 2003, 244 (02) :383-391