STRUCTURE SENSITIVE REACTIONS OVER SUPPORTED RUTHENIUM CATALYSTS DURING FISCHER-TROPSCH SYNTHESIS

被引:10
作者
ABREVAYA, H
COHN, MJ
TARGOS, WM
ROBOTA, HJ
机构
[1] UOP, DesPlaines, 60017, Illinois
[2] Allied Signal, DesPlaines, 60017, Illinois
关键词
REVERSE MICELLE; FISCHER-TROPSCH; RUTHENIUM; PARTICLE SIZE; WATER-GAS SHIFT; DISPERSION; AGGLOMERATION;
D O I
10.1007/BF00764501
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
Highly dispersed ruthenium catalysts can be prepared on alumina by aqueous impregnation of ruthenium. EXAFS at the K-edge showed that this type of catalyst, after calcination and reduction, consisted of ruthenium particles, which were about 0.8 nm in size. When highly dispersed on alumina, ruthenium appears to catalyze the water-gas shift reaction, which occurs subsequent to Fischer-Tropsch synthesis. The hydrocarbons produced had low olefinicity, possibly because of in situ production of hydrogen via the water-gas shift reaction. Highly dispersed ruthenium was not stable on alumina during Fischer-Tropsch synthesis. The ruthenium agglomeration on the alumina surface, as well as overall ruthenium loss from the catalyst, was attributed to the formation of a volatile ruthenium carbonyl species. Catalysts with about 85% of the ruthenium in the form of 3-7 nm particles were prepared on alumina by reverse micelle impregnation of ruthenium. These larger particles were stable against ruthenium carbonyl formation and, therefore, did not exhibit ruthenium agglomeration or loss of ruthenium. Catalysts with 3-7 nm ruthenium particles displayed a higher turnover number for hydrocarbon synthesis, higher olefinicity, and chain-growth probability and did not exhibit water-gas shift activity in contrast to ruthenium particles which were about 0.8 nm in size. The CO disproportionation measurements showed much less CO dissociation over highly dispersed ruthenium relative to 3-7 nm ruthenium particles. This phenomenon is consistent with the low activity, the low chain-growth probability and may also relate to the tendency to form ruthenium carbonyl that is observed with small ruthenium particles. The apparent water-gas shift activity of highly dispersed ruthenium can be explained by the low CO dissociation efficiency as well as by the proposed ability to dissociate the water molecule. © 1991 J.C. Baltzer A.G., Scientific Publishing Company.
引用
收藏
页码:183 / 195
页数:13
相关论文
共 11 条
[1]  
ABREVAYA H, 1987, Patent No. 4714692
[2]  
ABREVAYA H, 1987, 10TH N AM M CAT SOC, P97
[3]  
Anderson R.B., 1983, FISCHER TROPSCH SYNT
[4]   STRUCTURE SENSITIVITY OF HYDROCARBON SYNTHESIS FROM CO AND H2 [J].
BOUDART, M ;
MCDONALD, MA .
JOURNAL OF PHYSICAL CHEMISTRY, 1984, 88 (11) :2185-2195
[5]   INSITU INFRARED STUDY OF RU/SIO2 - THE EFFECT OF THE METAL DISPERSION AND PRESSURE ON THE CHAIN GROWTH IN THE FISCHER-TROPSCH REACTION [J].
FUKUSHIMA, T ;
FUJIMOTO, K ;
TOMINAGA, H .
APPLIED CATALYSIS, 1985, 14 (1-3) :95-99
[6]   EFFECTS OF DISPERSION ON THE ACTIVITY AND SELECTIVITY OF ALUMINA-SUPPORTED RUTHENIUM CATALYSTS FOR CARBON-MONOXIDE HYDROGENATION [J].
KELLNER, CS ;
BELL, AT .
JOURNAL OF CATALYSIS, 1982, 75 (02) :251-261
[7]   FISCHER-TROPSCH STUDY OF SUPPORTED RUTHENIUM CATALYSTS [J].
KING, DL .
JOURNAL OF CATALYSIS, 1978, 51 (03) :386-397
[8]   EFFECTS OF DISPERSION IN CARBON-MONOXIDE ADSORPTION AND CARBON-MONOXIDE HYDROGENATION OVER ALUMINA-SUPPORTED RUTHENIUM CATALYSTS [J].
OKUHARA, T ;
KIMURA, T ;
KOBAYASHI, K ;
MISONO, M ;
YONEDA, Y .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1984, 57 (04) :938-943
[9]   ROLE OF CHEMISORPTION IN FISCHER-TROPSCH SYNTHESIS [J].
PONEC, V ;
VANBARNEVELD, WA .
INDUSTRIAL & ENGINEERING CHEMISTRY PRODUCT RESEARCH AND DEVELOPMENT, 1979, 18 (04) :268-271
[10]   REACTIONS OF CARBON-MONOXIDE AND HYDROGEN ON CO, NI, RU, AND PD METALS [J].
RABO, JA ;
RISCH, AP ;
POUTSMA, ML .
JOURNAL OF CATALYSIS, 1978, 53 (03) :295-311