CO2 reforming of methane over zeolite-Y supported ruthenium catalysts

被引:38
作者
Portugal, UL
Marques, CMP
Araujo, ECC
Morales, EV
Giotto, MV
Bueno, JMC
机构
[1] UFSCar, DEQ, BR-13565905 Sao Carlos, SP, Brazil
[2] UFSCar, DQ, BR-13565905 Sao Carlos, SP, Brazil
[3] Univ Cent Las Villas, Santa Clara, Cuba
基金
巴西圣保罗研究基金会;
关键词
ruthenium catalyst; synthesis gas; methane reforming; zeolite Y; NMR;
D O I
10.1016/S0926-860X(99)00426-3
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
Ru/HY and Ru/NaY catalysts were prepared by ion-exchange from an aqueous solution of [Ru(NH3)(6)]Cl-3 The catalysts were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and nuclear magnetic resonance (NMR). The results showed that Si/AI ratio of the zeolite framework after use depends on the catalyst preparation procedure. Upon activation in He, Si/A1 ratio in Ru/NaY is similar to that of initial zeolite NaY. After exposure to reaction conditions, NMR data show dealumination, whose extent increases with Ru loading. Samples activated in He followed by ion exchange with NaNO3 (neutralization) and reactivated in CH4/CO2/N-2 undergo only slight dealumination. The results suggest that during reaction the charge compensating protons, generated during Ru reduction, cause dealumination, accompanied by local destruction of the zeolite structure. The structure of zeolite and Ru dispersion was therefore, stabilized and the catalyst specific activity increased by neutralizing the protons prior to use in CO2 reforming. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:173 / 183
页数:11
相关论文
共 30 条
[1]   MOLECULAR ASPECTS IN SYN-GAS PRODUCTION - THE CO2-REFORMING REACTION CASE [J].
BASINI, L ;
SANFILIPPO, D .
JOURNAL OF CATALYSIS, 1995, 157 (01) :162-178
[2]   Potential of zeolite supported rhodium catalysts for the CO2 reforming of CH4 [J].
Bhat, RN ;
Sachtler, WMH .
APPLIED CATALYSIS A-GENERAL, 1997, 150 (02) :279-296
[3]   CO2 reforming of CH4 over supported Ru catalysts [J].
Bradford, MCJ ;
Vannice, MA .
JOURNAL OF CATALYSIS, 1999, 183 (01) :69-75
[4]   Catalytic reforming of methane with carbon dioxide over nickel catalysts .1. Catalyst characterization and activity [J].
Bradford, MCJ ;
Vannice, MA .
APPLIED CATALYSIS A-GENERAL, 1996, 142 (01) :73-96
[5]   Catalytic activity and coke resistance in the carbon dioxide reforming of methane to synthesis gas over zeolite-supported Ni catalysts [J].
Chang, JS ;
Park, SE ;
Chon, HZ .
APPLIED CATALYSIS A-GENERAL, 1996, 145 (1-2) :111-124
[6]   Reforming of methane with carbon dioxide to synthesis gas over supported rhodium catalysts .2. A steady-state tracing analysis: Mechanistic aspects of the carbon and oxygen reaction pathways to form CO [J].
Efstathiou, AM ;
Kladi, A ;
Tsipouriari, VA ;
Verykios, XE .
JOURNAL OF CATALYSIS, 1996, 158 (01) :64-75
[7]   ACTIVATION OF CH4 AND ITS REACTION WITH CO2 OVER SUPPORTED RH CATALYSTS [J].
ERDOHELYI, A ;
CSERENYI, J ;
SOLYMOSI, F .
JOURNAL OF CATALYSIS, 1993, 141 (01) :287-299
[8]   Comparative study at low and medium reaction temperatures of syngas production by methane reforming with carbon dioxide over silica and alumina supported catalysts [J].
Ferreira-Aparicio, P ;
Guerrero-Ruiz, A ;
Rodriguez-Ramos, I .
APPLIED CATALYSIS A-GENERAL, 1998, 170 (01) :177-187
[9]  
FROMENT GF, 1990, CHEM REACTOR ANAL
[10]   THE ROLE OF CATALYST SUPPORT ON THE ACTIVITY OF NICKEL FOR REFORMING METHANE WITH CO2 [J].
GADALLA, AM ;
BOWER, B .
CHEMICAL ENGINEERING SCIENCE, 1988, 43 (11) :3049-3062