Formation of polychlorinated benzenes during the catalytic combustion of chlorobenzene using a Pt/γ-Al2O3 catalyst

被引:132
作者
van den Brink, RW [1 ]
Louw, R [1 ]
Mulder, P [1 ]
机构
[1] Leiden Univ, Leiden Inst Chem, Gorlaeus Labs, Ctr Chem & Environm, NL-2300 RA Leiden, Netherlands
关键词
platinum; chlorobenzene; aromatic compound; volatile organic compound (VOC); byproduct formation; chlorination; catalytic combustion;
D O I
10.1016/S0926-3373(97)00076-3
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
Pt/gamma-Al2O3 has been used for the complete catalytic oxidation of chlorobenzene, a model for chlorinated aromatic compounds present in flue gases. Complete conversion of chlorobenzene is reached at ca. 440 degrees C, but at this temperature substantial amounts of polychlorinated benzenes are formed. Only at 600 degrees C complete selectivity to carbon dioxide is achieved. The addition of 1.75% of water to the carrier gas reduces formation of polychlorinated benzenes and improves conversion. The oxygen partial pressure has a remarkable effect on byproduct formation: the amounts of polychlorinated benzenes rise sharply with increasing oxygen concentration. Total conversion of chlorobenzene remains stable, hence the selectivity to carbon dioxide increases with decreasing oxygen pressure. When the gamma-Al2O3 support alone is applied, complete conversion of chlorobenzene is reached only at ca. 550 degrees C, without production of polychlorinated benzenes. The selectivity to carbon oxides however is poor. So platinum seems to be responsible for the formation of polychlorinated benzenes, which we propose is brought about by chlorination of adsorbed (chloro)benzene-species through platinum (oxy) chlorides. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:219 / 226
页数:8
相关论文
共 46 条
[1]  
ACCOMAZZO MA, 1965, IND ENG CHEM PROC DD, V4, P425, DOI 10.1021/i260016a015
[2]   CATALYST DEACTIVATION DURING DEEP OXIDATION OF CHLOROHYDROCARBONS [J].
AGARWAL, SK ;
SPIVEY, JJ ;
BUTT, JB .
APPLIED CATALYSIS A-GENERAL, 1992, 82 (02) :259-275
[3]   REACTION OF METHYL-CHLORIDE WITH ALUMINA SURFACES - STUDY OF THE METHOXY SURFACE SPECIES BY TRANSMISSION INFRARED-SPECTROSCOPY [J].
BEEBE, TP ;
CROWELL, JE ;
YATES, JT .
JOURNAL OF PHYSICAL CHEMISTRY, 1988, 92 (05) :1296-1301
[4]   CATALYTIC DESTRUCTION OF CHLOROFLUOROCARBONS AND TOXIC CHLORINATED HYDROCARBONS [J].
BICKLE, GM ;
SUZUKI, T ;
MITARAI, Y .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1994, 4 (2-3) :141-153
[5]  
BOND GC, 1975, J APPL CHEM BIOTECHN, V25, P241
[6]   Destruction of chlorinated methanes by catalytic hydrolysis [J].
Bond, GC ;
RosaC, F .
CATALYSIS LETTERS, 1996, 39 (3-4) :261-263
[7]   OXIDATIVE CATALYSIS OF CHLORINATED HYDROCARBONS BY METAL-LOADED ACID CATALYSTS [J].
CHATTERJEE, S ;
GREENE, HL .
JOURNAL OF CATALYSIS, 1991, 130 (01) :76-85
[8]   Energetics of the homolytic C-H and C-Cl bond cleavages in polychlorobenzenes: The role of electronic and steric effects [J].
Cioslowski, J ;
Liu, GH ;
Moncrieff, D .
JOURNAL OF PHYSICAL CHEMISTRY A, 1997, 101 (05) :957-960
[9]   MECHANISM OF VAPOR-PHASE CHLORINATION OF BENZENE-DERIVATIVES [J].
DORREPAAL, W ;
LOUW, R .
INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 1978, 10 (03) :249-275
[10]  
DORRESTIJN E, UNPUB J APPL ANAL PY