Effects of gasification gas components on tar and ammonia decomposition over hot gas cleanup catalysts

被引:178
作者
Simell, PA [1 ]
Hepola, JO [1 ]
Krause, AOI [1 ]
机构
[1] HELSINKI UNIV TECHNOL,DEPT CHEM TECHNOL,FIN-02150 ESPOO,FINLAND
关键词
hot gas cleanup; tar decomposition; ammonia decomposition;
D O I
10.1016/S0016-2361(97)00109-9
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The tar and ammonia decomposition activities of dolomite, nickel catalyst, alumina and SiC were compared in different gas atmospheres. Tests were carried out in a fixed-bed tube reactor at 900 degrees C under 2.0 and 5 MPa pressure. Toluene was used as a tar model compound. The gas atmospheres studied were mixtures of nitrogen carrier, toluene and ammonia with H-2, H2O, CO, CO2, CO2 + H2O, H-2 + H2O or CO + CO2. A gasification gas mixture containing all the components was also used. The predominant reaction of toluene in the empty tube and over SiC and alumina was hydrocracking. With dolomite and nickel catalyst, steam and CO2 reforming types of reaction took place at high rate, CO2 reforming being the faster. However, in gasification gas the rates of steam and CO2 reforming reactions were lowered due to the inhibiting effect of CO, CO2 and H-2 Ammonia reacted readily with CO2 even with the inert reference materials and very rapidly over the nickel catalyst. The presence of toluene increased the ammonia reaction rate on the nickel catalyst. Ammonia decomposed in the gasification gas with the nickel catalyst at the same rate as in H-2 + H2O-N-2. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:1117 / 1127
页数:11
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