{"title":"流化床直接空气捕集过程中氧化钙捕集二氧化碳的动力学。","authors":"Bryan Kean Hong Ooi, Ewa J Marek","doi":"10.1021/acs.energyfuels.4c03770","DOIUrl":null,"url":null,"abstract":"<p><p>The bulk of research in carbon capture involves high CO<sub>2</sub> concentrations. This work instead describes the kinetics of CaO carbonation in mixtures with <i>p</i>CO<sub>2</sub> between 0.38 and 2.70 vol % and at temperatures between 400 and 650 °C. The reaction was studied in a bed of SiO<sub>2</sub> fluidized at flow rates corresponding to <i>U/U</i> <sub>mf</sub> of ∼4. Lower concentrations of CO<sub>2</sub> connected to the rates of mass transfer of CO<sub>2</sub> of the same order of magnitude as the rates of carbonation, thus, were eliminated from the kinetic analysis. The introduction of steam to the gas mixture (2 vol %) increased the rates of carbonation, demonstrating a pseudocatalytic effect, yet diminishing at higher temperatures. A rate expression generally accepted in the literature for high concentration CO<sub>2</sub> in CaO carbonation was assessed for its applicability at near-equilibrium conditions, demonstrating that the order of the rate expression changes between 0 and 1, increasing at higher temperatures. Using nonlinear regression, the experimental values were fitted to the Langmuir-Hinshelwood rate expression. The obtained parameters indicate CO<sub>2</sub> sorption and desorption being equilibrated, with the overall capture dominated mainly by slow kinetics of chemical reactions.</p>","PeriodicalId":35,"journal":{"name":"Energy & Fuels","volume":"38 22","pages":"22290-22297"},"PeriodicalIF":5.3000,"publicationDate":"2024-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11586902/pdf/","citationCount":"0","resultStr":"{\"title\":\"Kinetics of CO<sub>2</sub> Capture with Calcium Oxide during Direct Air Capture in a Fluidized Bed.\",\"authors\":\"Bryan Kean Hong Ooi, Ewa J Marek\",\"doi\":\"10.1021/acs.energyfuels.4c03770\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The bulk of research in carbon capture involves high CO<sub>2</sub> concentrations. This work instead describes the kinetics of CaO carbonation in mixtures with <i>p</i>CO<sub>2</sub> between 0.38 and 2.70 vol % and at temperatures between 400 and 650 °C. The reaction was studied in a bed of SiO<sub>2</sub> fluidized at flow rates corresponding to <i>U/U</i> <sub>mf</sub> of ∼4. Lower concentrations of CO<sub>2</sub> connected to the rates of mass transfer of CO<sub>2</sub> of the same order of magnitude as the rates of carbonation, thus, were eliminated from the kinetic analysis. The introduction of steam to the gas mixture (2 vol %) increased the rates of carbonation, demonstrating a pseudocatalytic effect, yet diminishing at higher temperatures. A rate expression generally accepted in the literature for high concentration CO<sub>2</sub> in CaO carbonation was assessed for its applicability at near-equilibrium conditions, demonstrating that the order of the rate expression changes between 0 and 1, increasing at higher temperatures. Using nonlinear regression, the experimental values were fitted to the Langmuir-Hinshelwood rate expression. The obtained parameters indicate CO<sub>2</sub> sorption and desorption being equilibrated, with the overall capture dominated mainly by slow kinetics of chemical reactions.</p>\",\"PeriodicalId\":35,\"journal\":{\"name\":\"Energy & Fuels\",\"volume\":\"38 22\",\"pages\":\"22290-22297\"},\"PeriodicalIF\":5.3000,\"publicationDate\":\"2024-09-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11586902/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Energy & Fuels\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.energyfuels.4c03770\",\"RegionNum\":3,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/11/21 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"ENERGY & FUELS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy & Fuels","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1021/acs.energyfuels.4c03770","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/21 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
Kinetics of CO2 Capture with Calcium Oxide during Direct Air Capture in a Fluidized Bed.
The bulk of research in carbon capture involves high CO2 concentrations. This work instead describes the kinetics of CaO carbonation in mixtures with pCO2 between 0.38 and 2.70 vol % and at temperatures between 400 and 650 °C. The reaction was studied in a bed of SiO2 fluidized at flow rates corresponding to U/Umf of ∼4. Lower concentrations of CO2 connected to the rates of mass transfer of CO2 of the same order of magnitude as the rates of carbonation, thus, were eliminated from the kinetic analysis. The introduction of steam to the gas mixture (2 vol %) increased the rates of carbonation, demonstrating a pseudocatalytic effect, yet diminishing at higher temperatures. A rate expression generally accepted in the literature for high concentration CO2 in CaO carbonation was assessed for its applicability at near-equilibrium conditions, demonstrating that the order of the rate expression changes between 0 and 1, increasing at higher temperatures. Using nonlinear regression, the experimental values were fitted to the Langmuir-Hinshelwood rate expression. The obtained parameters indicate CO2 sorption and desorption being equilibrated, with the overall capture dominated mainly by slow kinetics of chemical reactions.
期刊介绍:
Energy & Fuels publishes reports of research in the technical area defined by the intersection of the disciplines of chemistry and chemical engineering and the application domain of non-nuclear energy and fuels. This includes research directed at the formation of, exploration for, and production of fossil fuels and biomass; the properties and structure or molecular composition of both raw fuels and refined products; the chemistry involved in the processing and utilization of fuels; fuel cells and their applications; and the analytical and instrumental techniques used in investigations of the foregoing areas.