In-situ FTIR analysis on conventional and sorption-enhanced methanation (SEM) processes over Ni, Rh, and Ru-based catalyst systems

被引:1
作者
Gomez, Laura [1 ]
Nguyen-Quang, Minh [2 ]
Azzolina-Jury, Federico [3 ]
Martinez, Isabel [1 ]
Murillo, Ramon [1 ]
机构
[1] Spanish Natl Res Council, Inst Carboquim, Environm Res Grp, ICB CSIC, Miguel Luesma Castan 4, Zaragoza 50018, Spain
[2] Univ Liverpool, Dept Elect Engn & Elect, Liverpool L69 3GJ, England
[3] Normandie Univ, ENSICAEN, UNICAEN, CNRS,Lab Catalyse & Spectochim, F-14000 Caen, France
关键词
CO2; methanation; SEM; Nickel; In-situ FTIR; Reaction mechanism; SUBSTITUTE NATURAL-GAS; CO2; METHANATION; OPERANDO IR; ADSORPTION; ZEOLITE; MECHANISM; H2O; HYDROGENATION; TEMPERATURE; SELECTIVITY;
D O I
10.1016/j.apcata.2024.119733
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
In this work, the sorption -enhanced methanation (SEM) process, in which an H 2 O sorbent is combined with a catalyst to remove the produced H 2 O, allowing the reaction equilibrium to shift towards CH 4 , was implemented to enhance the conventional CO 2 methanation at lower temperature. Three commercial catalysts based on Rh, Ru and Ni were catalytically tested and examined via in -situ FTIR measurements. Based on the conventional tests, Nibased catalyst turned out to be the most efficient catalyst system (ca. 80% CO 2 conversion at 250 degrees C, GHSV = 509 Nml/h & sdot; g cat ) which, was then combined with the zeolites 4 A and 13X to maximise the production of CH 4 in SEM conditions. The best results pointed to zeolite 4 A since the zeolite 13X adsorbed a significant amount of CO 2 as a feed gas, which was chemisorbed on the surface of the zeolite favouring the formation of formates and carbonates during the regeneration step. However, the same reaction mechanism was proposed for conventional methanation and SEM process.
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页数:14
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