Surface basicity and catalytic performance on Ni/Ce-Zr-Al-O catalyst for CO2+CH4 reforming

被引:13
作者
Li, CL [1 ]
Fu, YL [1 ]
Bian, GZ [1 ]
机构
[1] Univ Sci & Technol China, Dept Phys Chem, Hefei 230026, Peoples R China
关键词
Ni catalyst; CO2+CH4 reforming; CO2-TPD; surface basicity; coke deposition; ALUMINA CATALYSTS; CARBON-DIOXIDE; CO2; METHANE; CH4;
D O I
10.3866/PKU.WHXB20031004
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
Ni/Ce-Zr-Al-O catalysts were prepared by hydrothermal synthesis method. The effect of NiO content on the basicity of catalyst was investigated by using H-2-TPD (temperature programmed desorption), DRIFTS (diffuse reflectance infrared Fourier transform spectroscopy), and CO2-TPD. The catalytic performance was tested and the amount of coke deposition was measured. The H-2-TPD result shows that the amount of Ni on the catalyst surface increases with the NiO content. DRIFT and CO2-TPD results show that the bicarbonate and carbonate are the predominant species of the CO2 chemisorptions. The addition of few Ni can promote obviously CO2 chemisorption and weaken the intensity of basicity. While Ni metal is preferable to reside on stronger basic site, the increase of NiO content can weaken the basicity, decrease the amount of basic site and weaken the CO2 adsorption performance. It weakens the performance of eliminating coke by mobile oxygen originated from CO2. So the catalytic activity of the sample with 7.0% (w) NiO decreases during reaction, the amount of coke deposition is much higher than that of the sample with 4.0% (w) NiO.
引用
收藏
页码:902 / 906
页数:5
相关论文
共 18 条
[1]  
[Anonymous], FREE ENERGY FORMATIO
[2]   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
[3]   CO2 reforming of CH4 [J].
Bradford, MCJ ;
Vannice, MA .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1999, 41 (01) :1-42
[4]   Methane reforming over Ni/Ce-ZrO2 catalysts:: effect of nickel content [J].
Dong, WS ;
Roh, HS ;
Jun, KW ;
Park, SE ;
Oh, YS .
APPLIED CATALYSIS A-GENERAL, 2002, 226 (1-2) :63-72
[5]   POTASSIUM-MODIFIED OSMIUM ALUMINA CATALYSTS [J].
FU, YL ;
KRAUS, L ;
ZAKI, MI ;
KAPPENSTEIN, C ;
TESCHE, B ;
KNOZINGER, H .
JOURNAL OF MOLECULAR CATALYSIS, 1988, 44 (02) :295-311
[6]   INTRINSIC DEFECTS OF TIO2(110) - INTERACTION WITH CHEMISORBED O2, H-2, CO, AND CO2 [J].
GOPEL, W ;
ROCKER, G ;
FEIERABEND, R .
PHYSICAL REVIEW B, 1983, 28 (06) :3427-3438
[7]  
HAYAKAWA T, 1999, APPL CATAQL A, V183, p28P
[8]   Suppression of carbon deposition in the CO2-reforming of CH4 by adding basic metal oxides to a Ni/Al2O3 catalyst [J].
Horiuchi, T ;
Sakuma, K ;
Fukui, T ;
Kubo, Y ;
Osaki, T ;
Mori, T .
APPLIED CATALYSIS A-GENERAL, 1996, 144 (1-2) :111-120
[9]   ALKALI-PROMOTED ALUMINA CATALYSTS .1. CHEMISORPTION AND OXYGEN-EXCHANGE OF CARBON-MONOXIDE AND CARBON-DIOXIDE ON POTASSIUM-PROMOTED ALUMINA CATALYSTS [J].
KRUPAY, BW ;
AMENOMIYA, Y .
JOURNAL OF CATALYSIS, 1981, 67 (02) :362-370
[10]  
LI CL, 2001, J MOL CATAL, V15, P351