CO production from CO2 and H2 via the rWGS reaction by thermochemical redox cycling in interconnected fluidized beds

被引:21
作者
Keller, Martin [1 ,2 ]
Otomo, Junichiro [1 ]
机构
[1] Univ Tokyo, Grad Sch Frontier Sci, 5-1-5 Kashiwanoha, Kashiwa, Chiba 2778563, Japan
[2] Natl Inst Adv Ind Sci & Technol, Res Inst Energy Frontier, 1-16 Onogawa, Tsukuba, Ibaraki 3058569, Japan
基金
日本学术振兴会; 日本科学技术振兴机构;
关键词
CO2; activation; Reverse water gas shift; Solar fuels; Circulating fluidized bed; WATER-GAS SHIFT; CHEMICAL-LOOPING COMBUSTION; PEROVSKITE OXIDES; CARBON-DIOXIDE; OXYGEN NONSTOICHIOMETRY; SYNGAS PRODUCTION; FUEL PRODUCTION; IRON-OXIDE; CONVERSION; STABILITY;
D O I
10.1016/j.jcou.2020.101191
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The reverse water gas shift (rWGS) reaction represents an attractive route for CO2 activation with H-2 to generate CO that can be used as an intermediate in the production of fuels and chemicals. Here, we investigate the implementation of the rWGS reaction via thermochemical redox cycling, in which the overall rWGS reaction is split up into two half reactions of reduction and oxidation of a metal/metal oxide solid material. This can be practically implemented by spatially separating the two half-reactions in a two-reactor circulating fluidized bed in which metal/metal oxide particles are continuously circulated between the two reactors and thus provide a net oxygen transport from one reactor to the other. In this context, we aim to answer the question whether it is more beneficial to exploit crystalline phase changes or oxygen non-stoichiometry in the material to transport oxygen, by process analysis based on thermodynamic data. We find that phase change materials offer a better potential process efficiency, however at the expense of an inflexible CO product purity. For all materials, a tradeoff exists between process efficiency and CO product purity, and we identify a number of promising phase change materials that populate this trade-off and appear suitable to produce a high enough CO concentration for industrial methanol synthesis without any further gas purification.
引用
收藏
页数:11
相关论文
共 73 条
[1]   Progress in Chemical-Looping Combustion and Reforming technologies [J].
Adanez, Juan ;
Abad, Alberto ;
Garcia-Labiano, Francisco ;
Gayan, Pilar ;
de Diego, Luis F. .
PROGRESS IN ENERGY AND COMBUSTION SCIENCE, 2012, 38 (02) :215-282
[2]   CATALYTIC COMBUSTION OF METHANE OVER VARIOUS PEROVSKITE-TYPE OXIDES [J].
ARAI, H ;
YAMADA, T ;
EGUCHI, K ;
SEIYAMA, T .
APPLIED CATALYSIS, 1986, 26 (1-2) :265-276
[3]   Utilisation of CO2 as a chemical feedstock:: opportunities and challenges [J].
Aresta, Michele ;
Dibenedetto, Angela .
DALTON TRANSACTIONS, 2007, (28) :2975-2992
[4]  
Basu Prabir., 2015, CIRCULATING FLUIDIZE, DOI DOI 10.1007/978-3-319-06173-3
[5]   MIXED OXIDES OF THE TYPE MO2 (FLUORITE)-M2O3 .1. OXYGEN DISSOCIATION PRESSURES AND PHASE RELATIONSHIPS IN THE SYSTEM CEO2-CE2O3 AT HIGH TEMPERATURES [J].
BEVAN, DJM ;
KORDIS, J .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1964, 26 (09) :1509-1523
[6]   Analytical Model of CeO2 Oxidation and Reduction [J].
Bulfin, B. ;
Lowe, A. J. ;
Keogh, K. A. ;
Murphy, B. E. ;
Luebben, O. ;
Krasnikov, S. A. ;
Shvets, I. V. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2013, 117 (46) :24129-24137
[7]   High-Flux Solar-Driven Thermochemical Dissociation of CO2 and H2O Using Nonstoichiometric Ceria [J].
Chueh, William C. ;
Falter, Christoph ;
Abbott, Mandy ;
Scipio, Danien ;
Furler, Philipp ;
Haile, Sossina M. ;
Steinfeld, Aldo .
SCIENCE, 2010, 330 (6012) :1797-1801
[8]  
Cordova J., 2016, HIGH TEMPERATURE CER, DOI [10.13140/RG.2.1.1272.2166, DOI 10.13140/RG.2.1.1272.2166]
[9]   Thermodynamic Analyses of a Moderate-Temperature Process of Carbon Dioxide Hydrogenation to Methanol via Reverse Water-Gas Shift with In Situ Water Removal [J].
Cui, Xiaoti ;
Kaer, Soren K. .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2019, 58 (24) :10559-10569
[10]   CO2 conversion by reverse water gas shift catalysis: comparison of catalysts, mechanisms and their consequences for CO2 conversion to liquid fuels [J].
Daza, Yolanda A. ;
Kuhn, John N. .
RSC ADVANCES, 2016, 6 (55) :49675-49691