Hydrogen and syn gas production via CO2 dry reforming of methane over Mg/La promoted Co-Ni/MSU-S catalyst

被引:35
作者
Amin, Roohul
Liu, Bingsi [1 ]
Huang, Zhao Biao
Zhao, Yin Chuan
机构
[1] Tianjin Univ, Dept Chem, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
xLa/Mg yCozNi/MSU-S catalyst; O-2-TPO; H-2 and syn gas production; CH4/CO2; reforming; Low coking; High stability; CARBON-DIOXIDE; NI CATALYSTS; MSU-S; SILICA; CH4; COMPOSITE; ZEOLITE; DEPOSITION; MCM-41; CTAB;
D O I
10.1016/j.ijhydene.2015.10.063
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
A series of xMg/La yCozNi/MSU-S catalysts were prepared by a sol gel method and characterized by means of N-2-physisorption, FT-IR, H-2-TPR, CO2-TPD, H-2-TPD, XRD, HRTEM, TG/DSC and O-2-TPO techniques. The catalytic performance of the catalysts was evaluated for H-2 and syn gas production at different temperatures at atmospheric pressure. The effect of reaction temperature, catalyst composition and performance of the catalyst were investigated during CO2 dry reforming reaction at 700-800 degrees C with GHSV of 2.4 x 10(4) mL/g(-1)h(-1). The results indicated that upon La, Mg and Co promotion, the Ni nanoparticles are highly dispersed on the mesoporous walls of MSU-S via strong interaction between metal ions and the HO-Si-groups of MSU-S. The presence of La2O3 in xLayCozNi/MSU-S results in enhancement of initial catalytic activity as compared to xMgyCozNi/MSU-S. It revealed that 3 La 2Co 7Ni/MSU-S performed the best with highest CH4 and CO2 conversion showing outstanding catalytic activity, greater stability and low coking for 50 h during 75 h time on stream at 750 degrees C. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:807 / 819
页数:13
相关论文
共 66 条
[1]   Highly ordered mesoporous MSU-SBEA/zeolite beta composite material [J].
Bagshaw, Stephen A. ;
Baxter, Neville I. ;
Brew, Daniel R. M. ;
Hosie, Camilla F. ;
Nie, Yuntong ;
Jaenicke, Stephan ;
Khuan, Chuah Gaik .
JOURNAL OF MATERIALS CHEMISTRY, 2006, 16 (23) :2235-2244
[2]   Pulse study of CO2 reforming of methane over LaNiO3 [J].
Batiot-Dupeyrat, C ;
Valderrama, G ;
Meneses, A ;
Martinez, F ;
Barrault, J ;
Tatibouët, JM .
APPLIED CATALYSIS A-GENERAL, 2003, 248 (1-2) :143-151
[3]   Effect of the basicity created by La2O3 addition on the catalytic properties of Co(O)/SiO2 in CH4+CO2 reaction [J].
Bouarab, R ;
Cherifi, O ;
Auroux, A .
THERMOCHIMICA ACTA, 2005, 434 (1-2) :69-73
[4]   Nanonickel particles supported on silica. Morphology effects on their surface and hydrogenating properties [J].
Boudjahem, AG ;
Monteverdi, S ;
Mercy, M ;
Bettahar, MM .
CATALYSIS LETTERS, 2004, 97 (3-4) :177-183
[5]  
Boudjahen AG, 2004, CATAL LETT, V84, P115
[6]   CO2 reforming of CH4 [J].
Bradford, MCJ ;
Vannice, MA .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1999, 41 (01) :1-42
[7]   CO2 reforming of CH4 over supported Ru catalysts [J].
Bradford, MCJ ;
Vannice, MA .
JOURNAL OF CATALYSIS, 1999, 183 (01) :69-75
[8]   INFRARED SPECTROSCOPIC INVESTIGATION OF TITANIUM IN ZEOLITES - A NEW ASSIGNMENT OF THE 960 CM(-1) BAND [J].
CAMBLOR, MA ;
CORMA, A ;
PEREZPARIENTE, J .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1993, (06) :557-559
[9]   Synthesis and characterization of several Ni/NiAl2O4 catalysts active for the 1,2,4-trichlorobenzene hydrodechlorination [J].
Cesteros, Y ;
Salagre, P ;
Medina, F ;
Sueiras, JE .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2000, 25 (04) :213-227
[10]   LARGE ENHANCEMENT IN METHANE-TO-SYNGAS CONVERSION ACTIVITY OF SUPPORTED NI CATALYSTS DUE TO PRECOATING OF CATALYST SUPPORTS WITH MGO, CAO OR RARE-EARTH-OXIDE [J].
CHOUDHARY, VR ;
UPHADE, BS ;
MAMMAN, AS .
CATALYSIS LETTERS, 1995, 32 (3-4) :387-390