Study of TiO2 deactivation during gaseous acetone photocatalytic oxidation

被引:69
作者
Vorontsov, AV
Kurkin, EN
Savinov, EN
机构
[1] Boreskov Inst Catalysis, Novosibirsk 630090, Russia
[2] Russian Acad Sci, Inst New Chem Problems, Chernogolovka 142432, Moskow Region, Russia
关键词
acetone photocatalytic oxidation; deactivation; kinetics;
D O I
10.1006/jcat.1999.2572
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 kinetics of the deep photocatalytic oxidation of acetone was studied, Special attention was paid to the thermal deactivation process, The rate of the reaction reaches a peak at about 100 degrees C. With increasing concentration of water vapor the peak shifts towards higher temperature, whereas with increasing acetone concentration the peak shifts towards lower temperature. An increase in water vapor concentration slightly decreases the rate of oxidation at 40 degrees C and increases it at temperatures above the rate maximum, The presence of two types of acetone adsorption sites was deduced from two nu(C=O) bands of adsorbed acetone at 1683 and 1710 cm(-1) and can explain the dependence of the rate on acetone concentration. The rate of oxidation increases at temperatures below the peak, mainly because of the increase in the rate coefficient at the sites of the first type. This behavior has been ascribed to the thermal oxidation of an intermediate of the photocatalytic process. Abrupt drop in rate at temperatures above the peak is due to the partial oxidation products of acetone thermal oxidation that modify the TiO2 surface. (C) 1999 Academic Press.
引用
收藏
页码:318 / 324
页数:7
相关论文
共 16 条
[1]   Photocatalytic destruction of VOCs in the gas-phase using titanium dioxide [J].
Alberici, RM ;
Jardim, WE .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1997, 14 (1-2) :55-68
[2]   STUDY OF OXYGEN ISOTOPIC EXCHANGE OVER UV IRRADIATED ANATASE SAMPLES AND COMPARISON WITH PHOTOOXIDATION OF ISOBUTANE INTO ACETONE [J].
COURBON, H ;
FORMENTI, M ;
PICHAT, P .
JOURNAL OF PHYSICAL CHEMISTRY, 1977, 81 (06) :550-554
[3]   Photocatalytic and thermal catalytic oxidation of acetaldehyde on Pt/TiO2 [J].
Falconer, JL ;
Magrini-Bair, KA .
JOURNAL OF CATALYSIS, 1998, 179 (01) :171-178
[4]  
FORMENTI M, 1971, CHEMTECH DEC, P680
[5]  
LYASHENKO LV, 1974, TEOR EKSP KHIM, V10, P186
[6]  
LYASHENKO LV, 1977, THEOR EXP CHEM, V13, P35
[7]   Selective photocatalytic destruction of airborne VOCs [J].
Muradov, NZ ;
TRaissi, A ;
Muzzey, D ;
Painter, CR ;
Kemme, MR .
SOLAR ENERGY, 1996, 56 (05) :445-453
[8]   Gas-phase heterogeneous photocatalytic oxidation of ethanol: Pathways and kinetic modeling [J].
Nimlos, MR ;
Wolfrum, EJ ;
Brewer, ML ;
Fennell, JA ;
Bintner, G .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1996, 30 (10) :3102-3110
[9]   HETEROGENEOUS PHOTOCATALYTIC OXIDATION OF GAS-PHASE ORGANICS FOR AIR PURIFICATION - ACETONE, 1-BUTANOL, BUTYRALDEHYDE, FORMALDEHYDE, AND META-XYLENE OXIDATION [J].
PERAL, J ;
OLLIS, DF .
JOURNAL OF CATALYSIS, 1992, 136 (02) :554-565
[10]   PHOTOCATALYTIC ACTIVITIES OF METAL-OXIDE SEMICONDUCTORS FOR OXYGEN ISOTOPE EXCHANGE AND OXIDATION REACTIONS [J].
SATO, S ;
KADOWAKI, T .
JOURNAL OF CATALYSIS, 1987, 106 (01) :295-300