Beda Rolandi, Mattia Piacentini, Riccardo Ometto, Alessandro Porta, Carlo Giorgio Visconti
{"title":"高促进型Fe-Zn-Cu-K催化剂CO2费托合成性能研究","authors":"Beda Rolandi, Mattia Piacentini, Riccardo Ometto, Alessandro Porta, Carlo Giorgio Visconti","doi":"10.1016/j.apcata.2025.120590","DOIUrl":null,"url":null,"abstract":"<div><div>A state-of-the-art Fischer-Tropsch 100Fe:10Zn:1Cu:4 K catalyst and catalysts promoted with higher Cu and K loadings were compared in terms of activity, selectivity and stability in the CO<sub>2</sub> Fischer-Tropsch synthesis. Higher promoter loadings increased selectivity towards heavier hydrocarbons, with a minor impact on activity at high conversion conditions. In such conditions, both catalysts samples experienced activity loss possibly due to iron carbide oxidation at high water partial pressure, but while the state-of-the-art catalyst had also selectivity affected, the highly promoted catalyst preserved heavy products selectivity. Notably, the highly promoted catalyst could be successfully rejuvenated <em>in-situ</em> by decreasing pressure and increasing temperature under CO<sub>2</sub>/H<sub>2</sub> flow. This procedure allowed to restore almost completely the initial activity while preserving an excellent C<sub>2</sub><sub>+</sub> hydrocarbon selectivity. On the contrary, the traditional Fischer-Tropsch catalyst, after the same rejuvenation treatment, showed a more pronounced selectivity shift towards lighter products. These findings can help in formulating stable catalysts that promote the one-pot synthesis of long chain hydrocarbons from CO<sub>2</sub> at industrially relevant conditions.</div></div>","PeriodicalId":243,"journal":{"name":"Applied Catalysis A: General","volume":"708 ","pages":"Article 120590"},"PeriodicalIF":4.8000,"publicationDate":"2025-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"On the performances of highly promoted Fe-Zn-Cu-K catalysts for CO2 Fischer-Tropsch synthesis\",\"authors\":\"Beda Rolandi, Mattia Piacentini, Riccardo Ometto, Alessandro Porta, Carlo Giorgio Visconti\",\"doi\":\"10.1016/j.apcata.2025.120590\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A state-of-the-art Fischer-Tropsch 100Fe:10Zn:1Cu:4 K catalyst and catalysts promoted with higher Cu and K loadings were compared in terms of activity, selectivity and stability in the CO<sub>2</sub> Fischer-Tropsch synthesis. Higher promoter loadings increased selectivity towards heavier hydrocarbons, with a minor impact on activity at high conversion conditions. In such conditions, both catalysts samples experienced activity loss possibly due to iron carbide oxidation at high water partial pressure, but while the state-of-the-art catalyst had also selectivity affected, the highly promoted catalyst preserved heavy products selectivity. Notably, the highly promoted catalyst could be successfully rejuvenated <em>in-situ</em> by decreasing pressure and increasing temperature under CO<sub>2</sub>/H<sub>2</sub> flow. This procedure allowed to restore almost completely the initial activity while preserving an excellent C<sub>2</sub><sub>+</sub> hydrocarbon selectivity. On the contrary, the traditional Fischer-Tropsch catalyst, after the same rejuvenation treatment, showed a more pronounced selectivity shift towards lighter products. These findings can help in formulating stable catalysts that promote the one-pot synthesis of long chain hydrocarbons from CO<sub>2</sub> at industrially relevant conditions.</div></div>\",\"PeriodicalId\":243,\"journal\":{\"name\":\"Applied Catalysis A: General\",\"volume\":\"708 \",\"pages\":\"Article 120590\"},\"PeriodicalIF\":4.8000,\"publicationDate\":\"2025-09-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Applied Catalysis A: General\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0926860X25004922\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Catalysis A: General","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0926860X25004922","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
On the performances of highly promoted Fe-Zn-Cu-K catalysts for CO2 Fischer-Tropsch synthesis
A state-of-the-art Fischer-Tropsch 100Fe:10Zn:1Cu:4 K catalyst and catalysts promoted with higher Cu and K loadings were compared in terms of activity, selectivity and stability in the CO2 Fischer-Tropsch synthesis. Higher promoter loadings increased selectivity towards heavier hydrocarbons, with a minor impact on activity at high conversion conditions. In such conditions, both catalysts samples experienced activity loss possibly due to iron carbide oxidation at high water partial pressure, but while the state-of-the-art catalyst had also selectivity affected, the highly promoted catalyst preserved heavy products selectivity. Notably, the highly promoted catalyst could be successfully rejuvenated in-situ by decreasing pressure and increasing temperature under CO2/H2 flow. This procedure allowed to restore almost completely the initial activity while preserving an excellent C2+ hydrocarbon selectivity. On the contrary, the traditional Fischer-Tropsch catalyst, after the same rejuvenation treatment, showed a more pronounced selectivity shift towards lighter products. These findings can help in formulating stable catalysts that promote the one-pot synthesis of long chain hydrocarbons from CO2 at industrially relevant conditions.
期刊介绍:
Applied Catalysis A: General publishes original papers on all aspects of catalysis of basic and practical interest to chemical scientists in both industrial and academic fields, with an emphasis onnew understanding of catalysts and catalytic reactions, new catalytic materials, new techniques, and new processes, especially those that have potential practical implications.
Papers that report results of a thorough study or optimization of systems or processes that are well understood, widely studied, or minor variations of known ones are discouraged. Authors should include statements in a separate section "Justification for Publication" of how the manuscript fits the scope of the journal in the cover letter to the editors. Submissions without such justification will be rejected without review.