scholarly journals A Dual Reactor for Isothermal Thermochemical Cycles of H2O/CO2 Co-Splitting Using La0.3Sr0.7Co0.7Fe0.3O3 as an Oxygen Carrier

Processes ◽  
2021 ◽  
Vol 9 (6) ◽  
pp. 1018
Author(s):  
Tatiya Khamhangdatepon ◽  
Thana Sornchamni ◽  
Nuchanart Siri-Nguan ◽  
Navadol Laosiripojana ◽  
Unalome Wetwatana Hartley

Catalytic performance of La0.3Sr0.7Co0.7Fe0.3O3 (LSCF3773 or LSCF) catalyst for syngas production via two step thermochemical cycles of H2O and CO2 co-splitting was investigated. Oxygen storage capacity (OSC) was found to depend on reduction temperature, rather than the oxidation temperature. The highest oxygen vacancy (Δδ) was achieved when the reduction and oxidation temperature were both fixed at 900 °C with the feed ratio (H2O to CO2) of 3 to 1, with an increasing amount of CO2 in the feed mixture. CO productivity reached its plateau at high ratios of H2O to CO2 (1:1, 1:2, and 1:2.5), while the total productivities were reduced with the same ratios. This indicated the existence of a CO2 blockage, which was the result of either high Ea of CO2 dissociation or high Ea of CO desorption, resulting in the loss in active species. From the results, it can be concluded that H2O and CO2 splitting reactions were competitive reactions. Ea of H2O and CO2 splitting was estimated at 31.01 kJ/mol and 48.05 kJ/mol, respectively, which agreed with the results obtained from the experimentation of the effect of the oxidation temperature. A dual-reactors system was applied to provide a continuous product stream, where the operation mode was switched between the reduction and oxidation step. The isothermal thermochemical cycles process, where the reduction and oxidation were performed at the same temperature, was also carried out in order to increase the overall efficiency of the process. The optimal time for the reduction and oxidation step was found to be 30 min for each step, giving total productivity of the syngas mixture at 28,000 μmol/g, approximately.

Fuel ◽  
2022 ◽  
Vol 309 ◽  
pp. 122100
Author(s):  
Ming Luo ◽  
Haiyan Zhang ◽  
Shuxiang Wang ◽  
Jianjun Cai ◽  
Yanjun Qin ◽  
...  

2020 ◽  
Vol 45 (2) ◽  
pp. 1267-1282 ◽  
Author(s):  
Ambrose Ugwu ◽  
Abdelghafour Zaabout ◽  
Julian R. Tolchard ◽  
Paul Inge Dahl ◽  
Shahriar Amini

2010 ◽  
Vol 22 (3) ◽  
pp. 851-859 ◽  
Author(s):  
A. Stamatiou ◽  
P. G. Loutzenhiser ◽  
A. Steinfeld

2019 ◽  
Vol 198 ◽  
pp. 111835 ◽  
Author(s):  
Tingting Xu ◽  
Bo Xiao ◽  
Gift Gladson Moyo ◽  
Fanghua Li ◽  
Zhihua Chen ◽  
...  

2021 ◽  
Vol 405 ◽  
pp. 126679
Author(s):  
Oscar Condori ◽  
Francisco García-Labiano ◽  
Luis F. de Diego ◽  
María T. Izquierdo ◽  
Alberto Abad ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
Kongzhai Li ◽  
Hua Wang ◽  
Yonggang Wei

Conversion of methane to syngas using a chemical-looping concept is a novel method for syngas generation. This process is based on the transfer of gaseous oxygen source to fuel (e.g., methane) by means of a cycling process using solid oxides as oxygen carriers to avoid direct contact between fuel and gaseous oxygen. Syngas is produced through the gas-solid reaction between methane and solid oxides (oxygen carriers), and then the reduced oxygen carriers can be regenerated by a gaseous oxidant, such as air or water. The oxygen carrier is recycled between the two steps, and the syngas with a ratio of H2/CO = 2.0 can be obtained successively. Air is used instead of pure oxygen allowing considerable cost savings, and the separation of fuel from the gaseous oxidant avoids the risk of explosion and the dilution of product gas with nitrogen. The design and elaboration of suitable oxygen carriers is a key issue to optimize this method. As one of the most interesting oxygen storage materials, ceria-based and perovskite oxides were paid much attention for this process. This paper briefly introduced the recent research progresses on the oxygen carriers used in the chemical-looping selective oxidation of methane (CLSOM) to syngas.


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