TY - JOUR
T1 - Multi-functional alumina-silica bimodal pore catalyst and its application for Fischer-Tropsch synthesis
AU - Zhang, Yi
AU - Koike, Masahiko
AU - Yang, Ruiqin
AU - Hinchiranan, Sukamon
AU - Vitidsant, Tharpong
AU - Tsubaki, Noritatsu
PY - 2005/9/18
Y1 - 2005/9/18
N2 - A multi-functional bimodal pore catalyst support, alumina-silica bimodal pore support, was prepared from a polymer complex solution and silica gel. The obtained bimodal pore support had two kinds of main pores; the pore volume was decreased and the specific surface area was enlarged, comparing with the original silica gel. This kind of bimodal pore support was applied in slurry phase Fischer-Tropsch synthesis, where cobalt was supported as active metal. Alumina-silica bimodal pore catalyst exhibited high catalytic activity and favorite selectivity, due to the spatial effects of bimodal pore structure and chemical effects of coexisting alumina, which formed the new small pores inside SiO2 large pores. Alumina-silica bimodal pore catalyst showed higher activity than silica-silica bimodal pore catalyst with similar pore structure, proving that hetero-atom bond between alumina and silica was important to promote the performance of the dispersed cobalt. The various catalysts were characterized by XRD, chemisorption, in situ DRIFT, TPR, and TPSR. It was found that alumina in alumina-silica bimodal structure improved cobalt dispersion significantly while keeping the reduction degree almost the same. TOF of alumina-silica bimodal catalysts was the highest, supported by the largest bridge-type adsorbed CO peak in DRIFT observation of this catalyst, as bridge-type adsorbed CO was the active intermediate in FTS.
AB - A multi-functional bimodal pore catalyst support, alumina-silica bimodal pore support, was prepared from a polymer complex solution and silica gel. The obtained bimodal pore support had two kinds of main pores; the pore volume was decreased and the specific surface area was enlarged, comparing with the original silica gel. This kind of bimodal pore support was applied in slurry phase Fischer-Tropsch synthesis, where cobalt was supported as active metal. Alumina-silica bimodal pore catalyst exhibited high catalytic activity and favorite selectivity, due to the spatial effects of bimodal pore structure and chemical effects of coexisting alumina, which formed the new small pores inside SiO2 large pores. Alumina-silica bimodal pore catalyst showed higher activity than silica-silica bimodal pore catalyst with similar pore structure, proving that hetero-atom bond between alumina and silica was important to promote the performance of the dispersed cobalt. The various catalysts were characterized by XRD, chemisorption, in situ DRIFT, TPR, and TPSR. It was found that alumina in alumina-silica bimodal structure improved cobalt dispersion significantly while keeping the reduction degree almost the same. TOF of alumina-silica bimodal catalysts was the highest, supported by the largest bridge-type adsorbed CO peak in DRIFT observation of this catalyst, as bridge-type adsorbed CO was the active intermediate in FTS.
KW - Alumina
KW - Bimodal pore support
KW - Cobalt catalyst
KW - Fischer-Tropsch synthesis
KW - Syngas
UR - http://www.scopus.com/inward/record.url?scp=24144481902&partnerID=8YFLogxK
U2 - 10.1016/j.apcata.2005.06.004
DO - 10.1016/j.apcata.2005.06.004
M3 - 学術論文
AN - SCOPUS:24144481902
SN - 0926-860X
VL - 292
SP - 252
EP - 258
JO - Applied Catalysis A: General
JF - Applied Catalysis A: General
IS - 1-2
ER -