Combustion of chlorinated hydrocarbons in catalyst-coated sintered metal fleece reactors

被引:26
作者
Everaert, K
Mathieu, M
Baeyens, J
Vansant, E
机构
[1] Catholic Univ Louvain, Dept Chem Engn, B-3001 Heverlee, Belgium
[2] Univ Instelling Antwerp, Catalysis Lab, UIA, B-2610 Wilrijk, Belgium
关键词
catalytic oxidation; chlorinated volatile organic compounds (CVOC); volatile organic compounds (VOC); fleece reactor; combustion;
D O I
10.1002/jctb.725
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Incinerators emit chlorinated hydrocarbons, such as polychlorinated benzenes (PCBz) and phenols (PCPh), polychlorinated biphenyls (PCB) and polychlorinated dibenzodioxins and furans (PCDD/F), as very dilute streams. High temperatures (>1000 degreesC) are required in traditional oxidizers. From an energy-saving perspective and to avoid de novo synthesis of PCDD/F, exhaust gas clean-up must be performed at low temperatures (250-350 degreesC). Catalytic combustion can be applied in this temperature range and different reactor layouts are used (eg monoliths, honeycomb). The present investigation uses a novel catalyst-coated sintered metal fleece. Thin metal fibers are sintered (non-woven) to fleece of various thickness, structure and porosity. V-Ti-W catalysts are examined. The paper will briefly review the catalyst coating method suitable to provide a structured fleece reactor with adequate characteristics. Experiments were carried out in the temperature range of 260-340 degreesC with various hydrocarbons injected in a carrier air stream. The experimental investigations demonstrated: (i) that the conversion of the hydrocarbons (volatile organic compounds, VOC) is independent of the oxygen concentration, corresponding to a zero-order dependence of the reaction rate; (ii) that the conversion of the hydrocarbons is a first-order reaction in the VOC; (iii) that the oxidation of the VOC proceeds to a greater extent with increasing temperature, with chlorine substitution enhancing the reactivity, and (iv) that the reaction rate constant follows an Arrhenius-dependence with activation energies between 37.3 and 58.4kJ mol(-1). An assessment of the results leads to a model expression with kinetic reaction control. This model can be used in a scale-up strategy. (C) 2003 Society of Chemical Industry.
引用
收藏
页码:167 / 172
页数:6
相关论文
共 21 条
[1]  
ARANZABAL A, 2000, P INT C CHISA 2000, P1
[2]   The formation and emission of dioxins in large scale thermal processes [J].
Everaert, K ;
Baeyens, J .
CHEMOSPHERE, 2002, 46 (03) :439-448
[3]  
FRINGS B, 1994, KATALYTISCHE DIOXIN, pK22
[4]  
Harley A., 1989, Process and catalyst for the dehydrochlorination of halogenated hydrocarbons [P], Patent No. [US4816609, 4816609]
[5]   CATALYTIC DESTRUCTION OF PCDDS PCFFS IN MUNICIPAL SOLID-WASTE FLUE-GAS [J].
HIRAOKA, M ;
TAKEDA, N ;
KASAKURA, T ;
IMOTO, Y ;
TSUBOI, H ;
IWASAKI, T .
CHEMOSPHERE, 1991, 23 (8-10) :1445-1452
[6]   METHYL-CHLORIDE AND METHYLENE-CHLORIDE INCINERATION IN A CATALYTICALLY STABILIZED THERMAL COMBUSTOR [J].
HUNG, SL ;
PFEFFERLE, LD .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1989, 23 (09) :1085-1091
[7]   Catalytic decomposition of dioxin from MSW incinerator flue gas [J].
Ide, Y ;
Kashiwabara, K ;
Okada, S ;
Mori, T ;
Hara, M .
CHEMOSPHERE, 1996, 32 (01) :189-198
[8]   DECOMPOSITION OF 1,2-DICHLOROETHANE ON TIO2/SIO2 [J].
IMAMURA, S ;
TARUMOTO, H ;
ISHIDA, S .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1989, 28 (10) :1449-1452
[9]  
JIANG X, 1996, APPL CATAL B-ENVIRON, V9, P226
[10]   The development of supported vanadia catalysts for the combined catalytic removal of the oxides of nitrogen and of chlorinated hydrocarbons from flue gases [J].
Jones, J ;
Ross, JRH .
CATALYSIS TODAY, 1997, 35 (1-2) :97-105