skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Development of alcohol-based synthetic transportation fuels from coal-derived synthesis gases. Third quarterly progress report, April 1-June 30, 1980

Technical Report ·
DOI:https://doi.org/10.2172/6747808· OSTI ID:6747808

Fourteen catalysts were prepared by either evaporation of metal nitrate-citric acid solutions or by impregnation of inert supports with metal nitrate-citric acid solutions. Fourteen catalysts were tested in either the Berty gradientless reactor or the plug-flow reactor. These catalysts have been characterized intto the following five groups: Group I - catalysts containing Cu, Zn, Co, Cr and alkali; Group II - catalysts of Group I without Zn or Co or Cr; Group III - modified methanol synthesis catalysts of substituted by transition metals such as Fe, Mn, Ti, Th, etc; and Group V - catalysts of Groups I, II or IV supported on refractory cements such as silica or titania. Although none of the catalysts tested this quarter resulted in reaching the targetted oxygenates selectivities and space time yields, the following relevant observations were made: Transition metals in a catalyst having the general atomic formula CuZn/sub 0/ /sub 125/CoK/sub 0/ /sub 11/M and produced by evaporation of metal nitrate - citric acid solution affect oxygenates selectivity as indicated below (in descending order), Fe approx. Cr > V >> Mn; Potassium in a catalyst having the formula Cu Zn/sub 0/ /sub 125/CoA/sub 0/ /sub 11/ is a better alkali promoter than cesium; Impregnation of inert supports with metal nitrate - citric acid solutions reduced activity and oxygenates productivity in comparison to the unsupported catalyst; Mechanical blending of metal oxides for a CuZn/sub 0/ /sub 125/CoCrK/sub 0/ /sub 11/ results in better selectivity-conversion characteristics than coprecipitation or evaporation of nitrate-citric acid solutions. For a CuZn/sub 0/ /sub 125/CoCrK/sub 0/ /sub 11/ catalyst reduced in situ in the presence of CO and CO/sub 2/ - containing syn gas, there was more than a two-fold increase in oxygenates selectivity over the 43 hour run period.

Research Organization:
Chem Systems, Inc., Fairfield, NJ (USA)
DOE Contract Number:
AC22-79ET14858
OSTI ID:
6747808
Report Number(s):
DOE/ET/14858-3
Country of Publication:
United States
Language:
English