Catalytic n-pentane conversion on H-ZSM-5 at high pressure

被引:11
|
作者
Schreiner, Edward P. [1 ]
Teketel, Shewangizaw [1 ]
Lobo, Raul F. [1 ]
机构
[1] Univ Delaware, Ctr Catalyt Sci & Technol, Dept Chem & Biomol Engn, Newark, DE 19716 USA
关键词
MONOMOLECULAR CRACKING; ENDOTHERMIC REACTIONS; TEMPERATURE; ZEOLITES; ALKANES; ZSM-5; DEHYDROGENATION; OLIGOMERIZATION; IMPROVEMENT; PROPANE;
D O I
10.1039/c5nj02733k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The effect of temperature (633-723 K), pressure (10-60 bar) and weight hourly space velocity (WHSV) (400-1500 g(C5) g(cat)(-1) h(-1)) on the conversion of n-pentane on H-[Al] ZSM-5 type catalysts has been investigated. Catalyst properties were tested using a packed-bed laboratory microreactor and reaction products were analyzed via online gas chromatography. 5-25% pentane conversion was observed at a pressure of 40 bar and temperatures in the range of 633-723 K. Reactant consumption rate approached saturation kinetics at pressures above 30 bar (similar to 14% conversion, 673 K). At 40 bar and 673 K, increasing WHSV (400-1500 g(C5) g(cat)(-1) h(-1)) resulted in a reduction in pentane conversion (26-10%). In all cases, propane and butane were the major products, followed by heavier C6+ compounds and other lighter products (C-1-C-4 paraffins and olefins). Propane carbon selectivity increased from 24% at 633 K to 34% at 723 K, while butane carbon selectivity (similar to 40%) was nearly constant. An inverse relationship between the production of C6+ and light products was observed with changes in reaction conditions. The carbon selectivity to C6+ compounds increased from 20% at 10 bar to 27% at 60 bar and decreased from 28% at 633 K to 18% at 723 K. At all reaction conditions, the observed product distribution can be explained as the result of fast bimolecular reactions, including hydride transfer and alkylation.
引用
收藏
页码:4245 / 4251
页数:7
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