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。

IF 5.3 3区 工程技术 Q2 ENERGY & FUELS
Energy & Fuels Pub Date : 2024-09-21 eCollection Date: 2024-11-21 DOI:10.1021/acs.energyfuels.4c03770
Bryan Kean Hong Ooi, Ewa J Marek
{"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}
引用次数: 0

摘要

碳捕集方面的大部分研究都涉及高浓度二氧化碳。本研究则描述了在 pCO2 在 0.38 至 2.70 Vol % 之间、温度在 400 至 650 °C 之间的混合物中氧化钙碳化的动力学。该反应是在流速为 U U/U mf ∼4 的二氧化硅流化床中进行研究的。二氧化碳浓度较低时,二氧化碳的传质速率与碳化速率的数量级相同,因此,动力学分析中不考虑二氧化碳浓度。在混合气体中引入蒸汽(2 体积%)会提高碳化速率,显示出一种假催化作用,但在温度升高时会减弱。对文献中普遍接受的高浓度二氧化碳在氧化钙碳化过程中的速率表达式进行了评估,以确定其在接近平衡条件下的适用性,结果表明速率表达式的阶数在 0 和 1 之间变化,温度越高,阶数越高。通过非线性回归,实验值被拟合到 Langmuir-Hinshelwood 速率表达式中。获得的参数表明,二氧化碳的吸附和解吸处于平衡状态,总体捕获主要由缓慢的化学反应动力学主导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Kinetics of CO<sub>2</sub> Capture with Calcium Oxide during Direct Air Capture in a Fluidized Bed.

Kinetics of CO<sub>2</sub> Capture with Calcium Oxide during Direct Air Capture in a Fluidized Bed.

Kinetics of CO<sub>2</sub> Capture with Calcium Oxide during Direct Air Capture in a Fluidized Bed.

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/U mf 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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Energy & Fuels
Energy & Fuels 工程技术-工程:化工
CiteScore
9.20
自引率
13.20%
发文量
1101
审稿时长
2.1 months
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信