@article { ISI:000230685200006, title = {Biphenyl hydrogenation over supported transition metal catalysts under supercritical carbon dioxide solvent}, journal = {Applied Catalysis A - General}, volume = {288}, number = {1-2}, year = {2005}, month = {JUL}, pages = {43-47}, publisher = {ELSEVIER SCIENCE BV}, type = {Article}, address = {PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS}, abstract = {

Catalytic hydrogenation of biphenyl to bicyclohexyl, an organic hydrogen storage medium, was examined over supported transition metal catalysts in supercritical carbon dioxide solvent. The yield of bicyclohexyl was almost 100\% over the charcoal-supported rhodium (Rh/C) and ruthenium (Ru/C) catalysts at the temperature of 323 K, which was much lower than that required for biphenyl hydrogenation in organic solvents (573 K). The initial activity was higher over the Rh/C catalyst, while the initial selectivity to bicyclohexyl was higher over the Ru/C catalyst. The conversion of biphenyl increased with increase in hydrogen and carbon dioxide pressures, while the selectivity to bicyclohexyl was independent of hydrogen and carbon dioxide pressures over both catalysts. (c) 2005 Elsevier B.V. All rights reserved.

}, keywords = {bicyclohexyl, biphenyl, charcoal-supported rhodium catalyst, charcoal-supported ruthenium catalyst, Hydrogen storage, Hydrogenation, Supercritical carbon dioxide}, issn = {0926-860X}, doi = {10.1016/j.apcata.2005.04.021}, author = {Hiyoshi, Norihito and Rode, C. V. and Sato, O. and Shirai, M.} } @article { ISI:000227710300073, title = {Enhanced selectivity to decalin in naphthalene hydrogenation under supercritical carbon dioxide}, journal = {Chemistry Letters}, volume = {34}, number = {3}, year = {2005}, month = {MAR}, pages = {424-425}, publisher = {CHEMICAL SOC JAPAN}, type = {Article}, address = {1-5 KANDA-SURUGADAI CHIYODA-KU, TOKYO, 101-8307, JAPAN}, abstract = {

A charcoal-supported rhodium catalyst was highly active and selective to decalin for the hydrogenation of naphthalene at very low temperature (333 K) under supercritical carbon dioxide.

}, issn = {0366-7022}, doi = {10.1246/cl.2005.424}, author = {Hiyoshi, Norihito and Miura, R. and Rode, C. V. and Sato, O. and Shirai, M.} } @article { ISI:000230232100019, title = {Partial ring hydrogenation of naphthols over supported metal catalysts in supercritical carbon dioxide solvent}, journal = {Chemistry Letters}, volume = {34}, number = {6}, year = {2005}, month = {JUN}, pages = {782-783}, publisher = {CHEMICAL SOC JAPAN}, type = {Article}, address = {1-5 KANDA-SURUGADAI CHIYODA-KU, TOKYO, 101-8307, JAPAN}, abstract = {

Selective ring hydrogenation of naphthols to tetrahydronaphthols and tetralones proceeded at 323 K over a charcoal supported rhodium catalyst in supercritical carbon dioxide.

}, issn = {0366-7022}, doi = {10.1246/cl.2005.782}, author = {Mine, Eiichi and Haryu, E. and Arai, K. and Sato, T. and Sato, O. and Sasaki, A. and Rode, C. V. and Shirai, M.} } @article { ISI:000238416100033, title = {Ring hydrogenation of naphthalene and 1-naphthol over supported metal catalysts in supercritical carbon dioxide solvent}, journal = {Catalysis Today}, volume = {115}, number = {1-4}, year = {2006}, note = {8th International Conference on Carbon Dioxide Utilization, Univ Oslo, Oslo, NORWAY, JUN 20-23, 2005}, month = {JUN}, pages = {248-253}, publisher = {ELSEVIER SCIENCE BV}, type = {Article}, address = {PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS}, abstract = {

Catalytic ring hydrogenations of naphthalene and 1-naphthol were studied over several supported metal catalysts in supercritical carbon dioxide solvent at low temperature. Higher concentration of hydrogen in supercritical carbon dioxide and lower reaction temperature were responsible for higher catalyst activity and selectivities to the desired partial ring hydrogenated products as compared with those observed in organic solvent for the same catalyst. (c) 2006 Elsevier B.V. All rights reserved.

}, keywords = {1-naphthol, Hydrogenation, Naphthalene, Supercritical carbon dioxide, supported metal catalyst}, issn = {0920-5861}, doi = {10.1016/j.cattod.2006.02.048}, author = {Shirai, M. and Rode, C. V. and Mine, Eiichi and Sasaki, A. and Sato, O. and Hiyoshi, Norihito} }