Evaluation of V2O5-WO3-TiO2 and alternative SCR catalysts in the abatement of VOCs

被引:56
作者
Busca, G
Baldi, M
Pistarino, C
Amores, JMG
Escribano, VS
Finocchio, E
Romezzano, G
Bregani, F
Toledo, GP
机构
[1] Univ Genoa, Dipartimento Ingn Chim & Proc, I-16129 Genoa, Italy
[2] Univ Pavia, Dipartimento Ingn Idraul & Ambientale, I-27100 Pavia, Italy
[3] Univ Salamanca, Dept Quim Inorgan, E-37008 Salamanca, Spain
[4] Dept Quim Inorgan, E-28040 Madrid, Spain
[5] ENEL SRI, PDM, I-20134 Milan, Italy
关键词
SCR catalysts; VOC; V(2)O(5)-WO(3)-TiO(2); Mn oxides; chlorinated hydrocarbons;
D O I
10.1016/S0920-5861(99)00140-6
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Two different commercial SCR catalysts belonging to the V(2)O(5)-WO(3)-TiO(2) system, and different alternative catalysts based on Mn, Fe, Cr, Al and Ti oxides have been tested in the conversion of VOCs in excess oxygen in a temperature range typical of the SCR process (500-700 K). Propane, propene, isopropanol, acetone, 2-chloropropane and 1,2-dichlorobenzene have been fed with excess oxygen and helium. The industrial catalysts are poorly active in the conversion of propane, giving mainly rise to propene by oxy-dehydrogenation. The conversion of propene is higher with CO as the predominant product. In any case, the oxidation activity depends on the vanadium content of the catalyst. Isopropanol is mainly converted into acetone and propene, while acetone is burnt predominantly to CO. Mn- and Fe- containing systems are definitely more active in the conversion of hydrocarbons and oxygenates, giving rise almost exclusively to CO(2). 2-Chloropropane is selectively dehydrochlorinated to propene and HCl starting from 350 K, propene being later burnt to CO on the industrial V(2)O(5)-WO(3)-TiO(2) catalysts, whose combustion activity is, apparently, not affected by chlorine. On the contrary, chlorine strongly affects the behavior of Mn-based catalysts, that are active in the dehydrochlorination of 2-chloropropane, but are simultaneously deactivated with respect to their combustion catalytic activity. The conversion of 1,2-dichlorobenzene gives rise to important amounts of heavy products in our experimental conditions with relatively high reactant concentration. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:525 / 533
页数:9
相关论文
共 38 条
[11]   Chemical and mechanistic aspects of the selective catalytic reduction of NOx by ammonia over oxide catalysts:: A review [J].
Busca, G ;
Lietti, L ;
Ramis, G ;
Berti, F .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1998, 18 (1-2) :1-36
[12]  
BUSCA G, 1994, STUD SURF SCI CATAL, V82, P777
[13]  
CARLSSON KB, 1992, CHEMOSPHERE, V25, P139
[14]  
CHO SM, 1994, CHEM ENG PROG, V90, P39
[15]  
Connell DW, 1997, BASIC CONCEPTS ENV C
[16]  
DICKSON L, 1989, CHEMOSPHERE, V19, P272
[17]  
Forzatti P, 1996, HETEROGEN CHEM REV, V3, P33, DOI 10.1002/(SICI)1234-985X(199603)3:1<33::AID-HCR54>3.0.CO
[18]  
2-R
[19]  
GERMAIN JE, 1972, B SOC CHIM FR, P4683
[20]  
GRZYBOWSKASWIER.B, 1998, CATAL TODAY, V157