TY - JOUR
T1 - Fischer-Tropsch synthesis using Co/SiO2 catalysts prepared from mixed precursors and addition effect of noble metals
AU - Sun, S.
AU - Fujimoto, K.
AU - Yoneyama, Y.
AU - Tsubaki, N.
N1 - Funding Information:
This work was partly supported by NEDO (contract number: 97E10005) and Sasakawa Scientific Research Grant from The Japan Science Society.
PY - 2002/7/8
Y1 - 2002/7/8
N2 - Fischer-Tropsch synthesis in Co/SiO2 catalysts, which were prepared by mixed impregnation of cobalt (II) nitrate and cobalt (II) acetate, was studied under mild reaction conditions (Total pressure = 1 MPa, H2/CO = 2, T = 513 K). X-ray diffraction indicated that highly dispersed cobalt metal was the main active sites on the catalyst prepared by the same method. It was considered that the metallic crystallines, which were readily reduced from cobalt nitrate, promoted the reduction of Co2+ to metallic a state in cobalt acetate by H2 spillover mechanism during the catalyst reduction process. The reduced cobalt, from cobalt acetate, was highly dispersed one and remarkably enhanced the catalytic activity. The addition of a small amount of Ru to this type of catalyst remarkably increased the catalytic activity and the reduction degree. Its turn over frequency (TOF) increased but the selectivity of CH4 was unchanged. However, when Pt or Pd were added into catalysts, they exhibited a higher selectivity of CH4. Although Pt and Pd hardly exerted an effect on cobalt reduction degree, they promoted cobalt dispersion and decreased the value of TOF. Characterization of these bimetallic catalysts suggested that a different contact between Co and Ru, Pt or Pd existed. Ru was enriched on the metallic cobalt surface but, Pt or Pd dispersed well in the form of Pt-Co or Pd-Co alloy.
AB - Fischer-Tropsch synthesis in Co/SiO2 catalysts, which were prepared by mixed impregnation of cobalt (II) nitrate and cobalt (II) acetate, was studied under mild reaction conditions (Total pressure = 1 MPa, H2/CO = 2, T = 513 K). X-ray diffraction indicated that highly dispersed cobalt metal was the main active sites on the catalyst prepared by the same method. It was considered that the metallic crystallines, which were readily reduced from cobalt nitrate, promoted the reduction of Co2+ to metallic a state in cobalt acetate by H2 spillover mechanism during the catalyst reduction process. The reduced cobalt, from cobalt acetate, was highly dispersed one and remarkably enhanced the catalytic activity. The addition of a small amount of Ru to this type of catalyst remarkably increased the catalytic activity and the reduction degree. Its turn over frequency (TOF) increased but the selectivity of CH4 was unchanged. However, when Pt or Pd were added into catalysts, they exhibited a higher selectivity of CH4. Although Pt and Pd hardly exerted an effect on cobalt reduction degree, they promoted cobalt dispersion and decreased the value of TOF. Characterization of these bimetallic catalysts suggested that a different contact between Co and Ru, Pt or Pd existed. Ru was enriched on the metallic cobalt surface but, Pt or Pd dispersed well in the form of Pt-Co or Pd-Co alloy.
KW - CO hydrogenation
KW - Co/SiO catalysts
KW - Fischer-Tropsch synthesis
KW - Noble metal
KW - Reduction degree
UR - http://www.scopus.com/inward/record.url?scp=0037043090&partnerID=8YFLogxK
U2 - 10.1016/S0016-2361(02)00090-X
DO - 10.1016/S0016-2361(02)00090-X
M3 - 学術論文
AN - SCOPUS:0037043090
SN - 0016-2361
VL - 81
SP - 1583
EP - 1591
JO - Fuel
JF - Fuel
IS - 11-12
ER -