High carbon-resistance Ni/CeAlO3-Al2O3 catalyst for CH4/CO2 reforming

被引:231
作者
Chen, Wei [1 ]
Zhao, Guofeng [1 ]
Xue, Qingsong [1 ]
Chen, Li [1 ]
Lu, Yong [1 ]
机构
[1] E China Normal Univ, Dept Chem, Shanghai Key Lab Green Chem & Chem Proc, Shanghai 200062, Peoples R China
关键词
Carbon dioxide; Methane; Syngas; Nickel catalyst; Cerium; Carbon; NI/AL2O3; CATALYSTS; SYNTHESIS GAS; METHANE; CO2; DECOMPOSITION; GASIFICATION; STATE; CERIA; DEACTIVATION; ENHANCEMENT;
D O I
10.1016/j.apcatb.2013.01.044
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
High carbon-resistance Ni/Ce-AlO catalysts have been developed for dry reforming of methane (DRM) that is attracting growing attention for chemical recycling of CO2 to fuels/chemicals. Cerium is definitely identified to exist in the form of CeAlO3 phase after reduction at 900 degrees C, and so is it under running conditions. The formation of CeAlO3 phase significantly enhances the catalyst carbon-resistance without decreasing the activity. Whereas the catalysts with or without CeAlO3 all show good activity maintenance within 250 h testing at 800 degrees C using 20,000 mL h(-1) g(cat)(-1), their carbon deposition amounts exhibit significant decrease from 0.92 to 0.29 g g(cat)(-1) along with the increase of the CeAlO3 phase. The presence of CeAlO3 can inhibit growth of graphitic carbon on nickel surface while the formation of amorphous carbon is independent of the CeAlO3. The CeAlO3 species shows ability for decomposing CO2 to form active surface oxygen and therefore the carbon-resistance promotion by nature is suggested to be contributed to an oxidative environment around Ni particles. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:260 / 268
页数:9
相关论文
共 52 条
[1]   Mechanisms for catalytic carbon nanofiber growth studied by ab initio density functional theory calculations [J].
Abild-Pedersen, F ;
Norskov, JK ;
Rostrup-Nielsen, JR ;
Sehested, J ;
Helveg, S .
PHYSICAL REVIEW B, 2006, 73 (11)
[2]   Methane activation on Ni(111):: Effects of poisons and step defects [J].
Abild-Pedersen, F ;
Lytken, O ;
Engbæk, J ;
Nielsen, G ;
Chorkendorff, I ;
Norskov, JK .
SURFACE SCIENCE, 2005, 590 (2-3) :127-137
[3]   PARTIAL OXIDATION OF METHANE TO SYNTHESIS GAS-USING CARBON-DIOXIDE [J].
ASHCROFT, AT ;
CHEETHAM, AK ;
GREEN, MLH ;
VERNON, PDF .
NATURE, 1991, 352 (6332) :225-226
[4]   CATALYTIC GROWTH OF CARBON FILAMENTS [J].
BAKER, RTK .
CARBON, 1989, 27 (03) :315-323
[5]   NUCLEATION AND GROWTH OF CARBON DEPOSITS FROM NICKEL CATALYZED DECOMPOSITION OF ACETYLENE [J].
BAKER, RTK ;
BARBER, MA ;
WAITE, RJ ;
HARRIS, PS ;
FEATES, FS .
JOURNAL OF CATALYSIS, 1972, 26 (01) :51-&
[6]   CARBON DEPOSITION IN STEAM REFORMING AND METHANATION [J].
BARTHOLOMEW, CH .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1982, 24 (01) :67-112
[7]   Steam reforming and graphite formation on Ni catalysts [J].
Bengaard, HS ;
Norskov, JK ;
Sehested, J ;
Clausen, BS ;
Nielsen, LP ;
Molenbroek, AM ;
Rostrup-Nielsen, JR .
JOURNAL OF CATALYSIS, 2002, 209 (02) :365-384
[8]   Deactivation and coke accumulation during CO2/CH4 reforming over Pt catalysts [J].
Bitter, JH ;
Seshan, K ;
Lercher, JA .
JOURNAL OF CATALYSIS, 1999, 183 (02) :336-343
[9]   The state of zirconia supported platinum catalysts for CO2/CH4 reforming [J].
Bitter, JH ;
Seshan, K ;
Lercher, JA .
JOURNAL OF CATALYSIS, 1997, 171 (01) :279-286
[10]   CO2 reforming of CH4 [J].
Bradford, MCJ ;
Vannice, MA .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1999, 41 (01) :1-42