Supported Nanostructured MoxC Materials for the Catalytic Reduction of CO2 through the Reverse Water Gas Shift Reaction

被引:12
作者
Pajares, Arturo [1 ,2 ,3 ,4 ]
Liu, Xianyun [1 ,2 ,5 ]
Busacker, Joan R. [1 ,2 ]
Ramirez de la Piscina, Pilar [1 ,2 ]
Homs, Narcis [1 ,2 ,3 ]
机构
[1] Univ Barcelona, Seccio Quim Inorgan, Dept Quim Inorgan & Organ, Marti i Franques 1, Barcelona 08028, Spain
[2] Univ Barcelona, Inst Nanociencia & Nanotecnol IN2UB, Marti i Franques 1, Barcelona 08028, Spain
[3] Catalonia Inst Energy Res IREC, Jardins Dones Negre 1, Barcelona 08930, Spain
[4] Flemish Inst Technol Res VITO NV, Sustainable Mat Management, Boeretang 200, B-2400 Mol, Belgium
[5] Henan Polytech Univ, Coll Chem & Chem Engn, Jiaozuo 454003, Henan, Peoples R China
关键词
CO2 catalytic reduction; syngas; RWGS; supported molybdenum carbide; MoxC-based catalysts; FISCHER-TROPSCH SYNTHESIS; CARBON-DIOXIDE CAPTURE; MOLYBDENUM CARBIDE; CONVERSION; HYDROGENATION; STORAGE; TUNGSTEN; RAMAN; NANOPARTICLES; PERFORMANCE;
D O I
10.3390/nano12183165
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
MoxC-based catalysts supported on gamma-Al2O3, SiO2 and TiO2 were prepared, characterized and studied in the reverse water gas shift (RWGS) at 548-673 K and atmospheric pressure, using CO2:H-2 = 1:1 and CO2:H-2 = 1:3 mol/mol reactant mixtures. The support used determined the crystalline MoxC phases obtained and the behavior of the supported nanostructured MoxC catalysts in the RWGS. All catalysts were active in the RWGS reaction under the experimental conditions used; CO productivity per mol of Mo was always higher than that of unsupported Mo2C prepared using a similar method in the absence of support. The CO selectivity at 673 K was above 94% for all the supported catalysts, and near 99% for the SiO2-supported. The MoxC/SiO2 catalyst, which contains a mixture of hexagonal Mo2C and cubic MoC phases, exhibited the best performance for CO production.
引用
收藏
页数:15
相关论文
共 63 条
[1]   Thiophene hydrodesulfurization over alumina-supported molybdenum carbide and nitride catalysts: Adsorption sites, catalytic activities, and nature of the active surface [J].
Aegerter, PA ;
Quigley, WWC ;
Simpson, GJ ;
Ziegler, DD ;
Logan, JW ;
McCrea, KR ;
Glazier, S ;
Bussell, ME .
JOURNAL OF CATALYSIS, 1996, 164 (01) :109-121
[2]  
[Anonymous], 2013, NEW FUTURE DEV CATAL, DOI DOI 10.1126/science.aal3573
[3]   Recent progress in syngas production via catalytic CO2 hydrogenation reaction [J].
Bahmanpour, Ali M. ;
Signorile, Matteo ;
Kroecher, Oliver .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2021, 295
[4]   MoO2/Multiwalled Carbon Nanotubes (MWCNT) Hybrid for Use as a Li-Ion Battery Anode [J].
Bhaskar, Akkisetty ;
Deepa, Melepurath ;
Rao, Tata Narasinga .
ACS APPLIED MATERIALS & INTERFACES, 2013, 5 (07) :2555-2566
[5]   Carbon capture and storage update [J].
Boot-Handford, M. E. ;
Abanades, J. C. ;
Anthony, E. J. ;
Blunt, M. J. ;
Brandani, S. ;
Mac Dowell, N. ;
Fernandez, J. R. ;
Ferrari, M. -C. ;
Gross, R. ;
Hallett, J. P. ;
Haszeldine, R. S. ;
Heptonstall, P. ;
Lyngfelt, A. ;
Makuch, Z. ;
Mangano, E. ;
Porter, R. T. J. ;
Pourkashanian, M. ;
Rochelle, G. T. ;
Shah, N. ;
Yao, J. G. ;
Fennell, P. S. .
ENERGY & ENVIRONMENTAL SCIENCE, 2014, 7 (01) :130-189
[6]   Micro-Raman study of the m-MoO2 to α-MoO3 transformation induced by cw-laser irradiation [J].
Camacho-Lopez, M. A. ;
Escobar-Alarcon, L. ;
Picquart, M. ;
Arroyo, R. ;
Cordoba, G. ;
Haro-Poniatowski, E. .
OPTICAL MATERIALS, 2011, 33 (03) :480-484
[7]   Nitrogen-doped Graphene-Supported Transition-metals Carbide Electrocatalysts for Oxygen Reduction Reaction [J].
Chen, Minghua ;
Liu, Jilei ;
Zhou, Weijiang ;
Lin, Jianyi ;
Shen, Zexiang .
SCIENTIFIC REPORTS, 2015, 5
[8]   A novel catalyst for hydrazine decomposition:: molybdenum carbide supported on γ-Al2O3 [J].
Chen, XW ;
Zhang, T ;
Ying, PL ;
Zheng, MY ;
Wu, WC ;
Xia, LG ;
Li, T ;
Wang, XD ;
Li, C .
CHEMICAL COMMUNICATIONS, 2002, (03) :288-289
[9]   Adsorbent Materials for Carbon Dioxide Capture from Large Anthropogenic Point Sources [J].
Choi, Sunho ;
Drese, Jeffrey H. ;
Jones, Christopher W. .
CHEMSUSCHEM, 2009, 2 (09) :796-854
[10]   Study of the temperature-programmed reaction synthesis of early transition metal carbide and nitride catalyst materials from oxide precursors [J].
Claridge, JB ;
York, APE ;
Brungs, AJ ;
Green, MLH .
CHEMISTRY OF MATERIALS, 2000, 12 (01) :132-142