Production of CO-Free H2 by Formic Acid Decomposition over Mo2C/Carbon Catalysts

被引:67
作者
Koos, Akos [1 ]
Solymosi, Frigyes [1 ]
机构
[1] Univ Szeged, Hungarian Acad Sci, Dept Phys Chem & Mat Sci,Chem Res Ctr, React Kinet Res Grp, H-6701 Szeged, Hungary
关键词
Pure hydrogen production; Formic acid decomposition; Mo2C catalyst; Multiwall carbon nanotube support; Carbon Norit support; HYDROGEN-PRODUCTION; MO2C/MO(100) SURFACE; METAL-OXIDES; FUEL-CELLS; METHANOL; CH4; ISOMERIZATION; POTASSIUM; RUTHENIUM; ETHANOL;
D O I
10.1007/s10562-010-0375-3
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
The vapor phase decomposition of formic acid was studied over supported Mo2C catalysts in a flow system. Mo2C deposited on silica is an effective catalyst for both the dehydrogenation of formic acid to yield H-2 and CO2, and its dehydration to yield H2O and CO. The extent of the decomposition approached 100% at 623 K. Preparation of the Mo2C catalyst by the reaction of MoO3 with a multiwall carbon nanotube and carbon Norit, however, dramatically altered the product distribution. Dehydrogenation became the dominant process. In optimum case, the selectivity for H-2, expressed in terms of the ratio CO2/CO + CO2, was 98-99%, even on total conversion at 423473 K. The addition of water to the formic acid completely eliminated CO formation and furnished CO-free H-2 on Mo2C/carbon catalysts at 373-473 K. Another feature of the Mo2C catalyst is its high stability. No changes in activity or selectivity were observed within 10 h.
引用
收藏
页码:23 / 27
页数:5
相关论文
共 32 条
[1]   LOW-TEMPERATURE CATALYTIC HOMOLOGATION OF METHANE ON PLATINUM, RUTHENIUM AND COBALT [J].
BELGUED, M ;
AMARIGLIO, H ;
PAREJA, P ;
AMARIGLIO, A ;
SAINTJUST, J .
CATALYSIS TODAY, 1992, 13 (2-3) :437-445
[2]  
Bond G.C., 1962, CATALYSIS METALS
[3]   In situ TPO, TPD and XRD characterisation of a molybdenum oxycarbohydride catalyst for n-butane isomerisation [J].
Bouchy, C ;
Pham-Huu, C ;
Heinrich, B ;
Derouane, EG ;
Derouane-Abd Hamid, SB ;
Ledoux, MJ .
APPLIED CATALYSIS A-GENERAL, 2001, 215 (1-2) :175-184
[4]   Microstructure and characterization of a highly selective catalyst for the isomerization of alkanes: A molybdenum oxycarbide [J].
Bouchy, C ;
Pham-Huu, C ;
Heinrich, B ;
Chaumont, C ;
Ledoux, MJ .
JOURNAL OF CATALYSIS, 2000, 190 (01) :92-103
[5]   Spectroscopic study on the formation of CO2- on K-promoted Mo2C/Mo(100) surface [J].
Bugyi, L ;
Oszkó, A ;
Solymosi, F .
SURFACE SCIENCE, 2000, 461 (1-3) :177-190
[6]   Electro-oxidation of methanol and formic acid on PtRu and PtAu for direct liquid fuel cells [J].
Choi, Jong-Ho ;
Jeong, Kyoung-Jin ;
Dong, Yujung ;
Han, Jonghee ;
Lim, Tae-Hoon ;
Lee, Jae-Suk ;
Sung, Yung-Eun .
JOURNAL OF POWER SOURCES, 2006, 163 (01) :71-75
[7]   THE INTERACTION OF FORMIC-ACID WITH TRANSITION-METAL SURFACES, STUDIED IN ULTRAHIGH-VACUUM [J].
COLUMBIA, MR ;
THIEL, PA .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1994, 369 (1-2) :1-14
[8]   Quantitative determination of the catalytic activity of bulk metal oxides for formic acid oxidation [J].
Fein, DE ;
Wachs, IE .
JOURNAL OF CATALYSIS, 2002, 210 (02) :241-254
[9]   A viable hydrogen-storage system based on selective formic acid decomposition with a ruthenium catalyst [J].
Fellay, Celine ;
Dyson, Paul J. ;
Laurenczy, Gabor .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (21) :3966-3968
[10]   Current status of hydrogen production techniques by steam reforming of ethanol: A review [J].
Haryanto, A ;
Fernando, S ;
Murali, N ;
Adhikari, S .
ENERGY & FUELS, 2005, 19 (05) :2098-2106