{"title":"Al2O3/MgO掺杂,CaO基吸附剂捕集CO2:性能研究","authors":"Chengzhuang Zhang, Jia Fang, Xilong Xu, Meng Zhang, Zhiqiang Han, Jianxiong Liao","doi":"10.1111/nyas.70026","DOIUrl":null,"url":null,"abstract":"We investigated direct calcination of four precursors: calcium oxalate (CaC<jats:sub>2</jats:sub>O<jats:sub>4</jats:sub>; denoted as CaO‐1), calcium carbonate (CaCO<jats:sub>3</jats:sub>; CaO‐2), calcium <jats:sc>d</jats:sc>‐gluconate monohydrate (C<jats:sub>12</jats:sub>H<jats:sub>22</jats:sub>CaO<jats:sub>14</jats:sub>·H<jats:sub>2</jats:sub>O; CaO‐3), and a commercial calcium carbonate (CaO‐4). The effects of precursor selection on CO<jats:sub>2</jats:sub> adsorption performance were systematically compared. CaO‐1 exhibited superior initial CO<jats:sub>2</jats:sub> adsorption capacity (0.63 g/g) due to hierarchical porosity, but suffered a 38% capacity loss after 10 cycles from sintering. Al<jats:sub>2</jats:sub>O<jats:sub>3</jats:sub> doping (CaO–Al<jats:sub>2</jats:sub>O<jats:sub>3</jats:sub>, 95/5) enhanced capacity and kinetics (0.65 g/g and 0.23 g/g·min<jats:sup>−1</jats:sup>, respectively), showing 3% and 43.75% improvements over CaO‐1, respectively, though a degradation of 33.8% occurred after 20 cycles. MgO doping (CaO–MgO, 85/15) achieved exceptional cyclic stability, retaining 93% capacity over 10 cycles (55% improvement vs. CaO‐1) via inherent sintering resistance. Characterization experiments confirmed their structural evolution: Al<jats:sub>2</jats:sub>O<jats:sub>3</jats:sub> stabilized pore networks, while MgO preserved framework integrity. The results demonstrate that precursor engineering and dopant selection critically influence adsorption kinetics versus cyclic stability trade‐offs. Optimal CaO–Al<jats:sub>2</jats:sub>O<jats:sub>3</jats:sub> (95/5) and CaO–MgO (85/15) compositions propose a kinetics–stability decoupling strategy. This dual‐dopant approach addresses calcium looping challenges by balancing rapid CO<jats:sub>2</jats:sub> capture with structural durability, providing insights for cost‐effective adsorbent optimization.","PeriodicalId":8250,"journal":{"name":"Annals of the New York Academy of Sciences","volume":"38 1","pages":""},"PeriodicalIF":4.8000,"publicationDate":"2025-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Al2O3/MgO‐doped, CaO‐based adsorbents for CO2 capture: A performance study\",\"authors\":\"Chengzhuang Zhang, Jia Fang, Xilong Xu, Meng Zhang, Zhiqiang Han, Jianxiong Liao\",\"doi\":\"10.1111/nyas.70026\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"We investigated direct calcination of four precursors: calcium oxalate (CaC<jats:sub>2</jats:sub>O<jats:sub>4</jats:sub>; denoted as CaO‐1), calcium carbonate (CaCO<jats:sub>3</jats:sub>; CaO‐2), calcium <jats:sc>d</jats:sc>‐gluconate monohydrate (C<jats:sub>12</jats:sub>H<jats:sub>22</jats:sub>CaO<jats:sub>14</jats:sub>·H<jats:sub>2</jats:sub>O; CaO‐3), and a commercial calcium carbonate (CaO‐4). The effects of precursor selection on CO<jats:sub>2</jats:sub> adsorption performance were systematically compared. CaO‐1 exhibited superior initial CO<jats:sub>2</jats:sub> adsorption capacity (0.63 g/g) due to hierarchical porosity, but suffered a 38% capacity loss after 10 cycles from sintering. Al<jats:sub>2</jats:sub>O<jats:sub>3</jats:sub> doping (CaO–Al<jats:sub>2</jats:sub>O<jats:sub>3</jats:sub>, 95/5) enhanced capacity and kinetics (0.65 g/g and 0.23 g/g·min<jats:sup>−1</jats:sup>, respectively), showing 3% and 43.75% improvements over CaO‐1, respectively, though a degradation of 33.8% occurred after 20 cycles. MgO doping (CaO–MgO, 85/15) achieved exceptional cyclic stability, retaining 93% capacity over 10 cycles (55% improvement vs. CaO‐1) via inherent sintering resistance. Characterization experiments confirmed their structural evolution: Al<jats:sub>2</jats:sub>O<jats:sub>3</jats:sub> stabilized pore networks, while MgO preserved framework integrity. The results demonstrate that precursor engineering and dopant selection critically influence adsorption kinetics versus cyclic stability trade‐offs. Optimal CaO–Al<jats:sub>2</jats:sub>O<jats:sub>3</jats:sub> (95/5) and CaO–MgO (85/15) compositions propose a kinetics–stability decoupling strategy. This dual‐dopant approach addresses calcium looping challenges by balancing rapid CO<jats:sub>2</jats:sub> capture with structural durability, providing insights for cost‐effective adsorbent optimization.\",\"PeriodicalId\":8250,\"journal\":{\"name\":\"Annals of the New York Academy of Sciences\",\"volume\":\"38 1\",\"pages\":\"\"},\"PeriodicalIF\":4.8000,\"publicationDate\":\"2025-08-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annals of the New York Academy of Sciences\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://doi.org/10.1111/nyas.70026\",\"RegionNum\":3,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of the New York Academy of Sciences","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1111/nyas.70026","RegionNum":3,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
Al2O3/MgO‐doped, CaO‐based adsorbents for CO2 capture: A performance study
We investigated direct calcination of four precursors: calcium oxalate (CaC2O4; denoted as CaO‐1), calcium carbonate (CaCO3; CaO‐2), calcium d‐gluconate monohydrate (C12H22CaO14·H2O; CaO‐3), and a commercial calcium carbonate (CaO‐4). The effects of precursor selection on CO2 adsorption performance were systematically compared. CaO‐1 exhibited superior initial CO2 adsorption capacity (0.63 g/g) due to hierarchical porosity, but suffered a 38% capacity loss after 10 cycles from sintering. Al2O3 doping (CaO–Al2O3, 95/5) enhanced capacity and kinetics (0.65 g/g and 0.23 g/g·min−1, respectively), showing 3% and 43.75% improvements over CaO‐1, respectively, though a degradation of 33.8% occurred after 20 cycles. MgO doping (CaO–MgO, 85/15) achieved exceptional cyclic stability, retaining 93% capacity over 10 cycles (55% improvement vs. CaO‐1) via inherent sintering resistance. Characterization experiments confirmed their structural evolution: Al2O3 stabilized pore networks, while MgO preserved framework integrity. The results demonstrate that precursor engineering and dopant selection critically influence adsorption kinetics versus cyclic stability trade‐offs. Optimal CaO–Al2O3 (95/5) and CaO–MgO (85/15) compositions propose a kinetics–stability decoupling strategy. This dual‐dopant approach addresses calcium looping challenges by balancing rapid CO2 capture with structural durability, providing insights for cost‐effective adsorbent optimization.
期刊介绍:
Published on behalf of the New York Academy of Sciences, Annals of the New York Academy of Sciences provides multidisciplinary perspectives on research of current scientific interest with far-reaching implications for the wider scientific community and society at large. Each special issue assembles the best thinking of key contributors to a field of investigation at a time when emerging developments offer the promise of new insight. Individually themed, Annals special issues stimulate new ways to think about science by providing a neutral forum for discourse—within and across many institutions and fields.