Syed Saqline , Haiming Wang , Qianwenhao Fan , Felix Donat , Christoph Müller , Wen Liu
{"title":"Investigation of barium iron oxides for CO2 capture and chemical looping oxygen uncoupling","authors":"Syed Saqline , Haiming Wang , Qianwenhao Fan , Felix Donat , Christoph Müller , Wen Liu","doi":"10.1016/j.jaecs.2023.100238","DOIUrl":null,"url":null,"abstract":"<div><p>The performance of two underexploited ternary oxides – Ba<sub>3</sub>Fe<sub>2</sub>O<sub>6</sub> and Ba<sub>5</sub>Fe<sub>2</sub>O<sub>8</sub> are investigated for carbon dioxide capture and chemical looping oxygen uncoupling. The ternary compound Ba<sub>3</sub>Fe<sub>2</sub>O<sub>6</sub> was found to have a structure characterised by space group <em>Pa</em><span><math><mover><mn>3</mn><mo>¯</mo></mover></math></span>. Experimental results have shown that both Ba<sub>3</sub>Fe<sub>2</sub>O<sub>6</sub> and Ba<sub>5</sub>Fe<sub>2</sub>O<sub>8</sub> are capable of cyclically capturing CO<sub>2</sub> at temperatures above 800 °C. Ba<sub>5</sub>Fe<sub>2</sub>O<sub>8</sub> demonstrated superior CO<sub>2</sub> capture performance compared to Ba<sub>3</sub>Fe<sub>2</sub>O<sub>6</sub>, with consistent gravimetric CO<sub>2</sub> uptake capacities of 4.35 wt% and 13.39 wt% at 900 °C and 1000 °C, respectively, over 20 cycles. In comparison, Ba<sub>3</sub>Fe<sub>2</sub>O<sub>6</sub> demonstrated high initial CO<sub>2</sub> uptake capacities which deteriorated cyclically, with 20 cycle average capacities of 7.73 wt% and 11.99 wt% at 900 °C and 1000 °C, respectively. Ba<sub>3</sub>Fe<sub>2</sub>O<sub>6</sub> also exhibits excellent recyclability and satisfactory chemical looping oxygen uncoupling (CLOU) activity over temperature swing cycles between 550 °C and 950 °C. In contrast, the strong affinity with CO<sub>2</sub> makes Ba<sub>5</sub>Fe<sub>2</sub>O<sub>8</sub> unsuitable for application in chemical looping oxygen uncoupling or chemical looping air separation, especially in the presence of substantial partial pressures of CO<sub>2</sub>.</p></div>","PeriodicalId":100104,"journal":{"name":"Applications in Energy and Combustion Science","volume":"17 ","pages":"Article 100238"},"PeriodicalIF":5.0000,"publicationDate":"2023-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2666352X23001279/pdfft?md5=0bc3d8f866208447e2f4a8e0531e589f&pid=1-s2.0-S2666352X23001279-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applications in Energy and Combustion Science","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666352X23001279","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
引用次数: 0
Abstract
The performance of two underexploited ternary oxides – Ba3Fe2O6 and Ba5Fe2O8 are investigated for carbon dioxide capture and chemical looping oxygen uncoupling. The ternary compound Ba3Fe2O6 was found to have a structure characterised by space group Pa. Experimental results have shown that both Ba3Fe2O6 and Ba5Fe2O8 are capable of cyclically capturing CO2 at temperatures above 800 °C. Ba5Fe2O8 demonstrated superior CO2 capture performance compared to Ba3Fe2O6, with consistent gravimetric CO2 uptake capacities of 4.35 wt% and 13.39 wt% at 900 °C and 1000 °C, respectively, over 20 cycles. In comparison, Ba3Fe2O6 demonstrated high initial CO2 uptake capacities which deteriorated cyclically, with 20 cycle average capacities of 7.73 wt% and 11.99 wt% at 900 °C and 1000 °C, respectively. Ba3Fe2O6 also exhibits excellent recyclability and satisfactory chemical looping oxygen uncoupling (CLOU) activity over temperature swing cycles between 550 °C and 950 °C. In contrast, the strong affinity with CO2 makes Ba5Fe2O8 unsuitable for application in chemical looping oxygen uncoupling or chemical looping air separation, especially in the presence of substantial partial pressures of CO2.