Jia Wang, Wen-Cui Li, Andi Di, Li-Dong Zhao, Danhui Sun, Lei He and An-Hui Lu*,
{"title":"通过中间体富集C4醛促进缺钙中孔羟基磷灰石乙醇升级C6-12高醇收率","authors":"Jia Wang, Wen-Cui Li, Andi Di, Li-Dong Zhao, Danhui Sun, Lei He and An-Hui Lu*, ","doi":"10.1021/acscatal.5c0144910.1021/acscatal.5c01449","DOIUrl":null,"url":null,"abstract":"<p >Ethanol upgrading to C<sub>6–12</sub> alcohols offers a green pathway to high-valued chemicals. Achieving high yields of C<sub>6–12</sub> alcohols remains challenging due to the complexity of the ethanol reaction network. Here, we report an efficient conversion of ethanol to C<sub>6–12</sub> alcohols using Ca-deficient mesoporous hydroxyapatite as the catalyst, which was prepared from the reaction of NH<sub>3</sub> and PO<sub>4</sub><sup>3–</sup>. The yield of C<sub>6–12</sub> alcohols reached 34.5% with a selectivity of 59.3% at 325 °C and 0.1 MPa, exhibiting a high ethanol upgrading performance. Ethanol adsorption kinetics and ethanol-TPD-DRIFT results revealed that the ethanol diffusional time constant of the enlarged pore of the hydroxyapatite increased by 2.01 folds of the original hydroxyapatite, thereby facilitating the access of ethanol molecules to active sites, which was beneficial for ethanol dehydrogenation. The online-generated acetaldehyde was subsequently undergoing aldol condensation to accelerate the formation of C<sub>4</sub> aldehydes, which, as the intermediates, were stabilized over Ca deficiency sites on the hydroxyapatite surface. The enriched C<sub>4</sub> aldehyde intermediates are further coupled with C<sub>2</sub>, C<sub>4</sub>, or C<sub>6</sub> aldehydes at the basic sites to produce longer-chain aldehydes (C ≥ 6), which are subsequently hydrogenated to form C<sub>6–12</sub> alcohols. Noticeably, compared to the original hydroxyapatite, the Ca-deficient hydroxyapatite showed enhanced density of basic sites, about two times higher. Hence, this catalyst remarkably boosted the yield of C<sub>6–12</sub> alcohols from ethanol upgrading. This work provides a strategy for the selective conversion of ethanol to C<sub>6–12</sub> alcohols.</p>","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":"15 10","pages":"8599–8610 8599–8610"},"PeriodicalIF":13.1000,"publicationDate":"2025-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Boosting C6–12 Higher Alcohols Yield from Ethanol Upgrading over Ca-Deficient Mesoporous Hydroxyapatite through Intermediates Enrichment of C4 Aldehyde\",\"authors\":\"Jia Wang, Wen-Cui Li, Andi Di, Li-Dong Zhao, Danhui Sun, Lei He and An-Hui Lu*, \",\"doi\":\"10.1021/acscatal.5c0144910.1021/acscatal.5c01449\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Ethanol upgrading to C<sub>6–12</sub> alcohols offers a green pathway to high-valued chemicals. Achieving high yields of C<sub>6–12</sub> alcohols remains challenging due to the complexity of the ethanol reaction network. Here, we report an efficient conversion of ethanol to C<sub>6–12</sub> alcohols using Ca-deficient mesoporous hydroxyapatite as the catalyst, which was prepared from the reaction of NH<sub>3</sub> and PO<sub>4</sub><sup>3–</sup>. The yield of C<sub>6–12</sub> alcohols reached 34.5% with a selectivity of 59.3% at 325 °C and 0.1 MPa, exhibiting a high ethanol upgrading performance. Ethanol adsorption kinetics and ethanol-TPD-DRIFT results revealed that the ethanol diffusional time constant of the enlarged pore of the hydroxyapatite increased by 2.01 folds of the original hydroxyapatite, thereby facilitating the access of ethanol molecules to active sites, which was beneficial for ethanol dehydrogenation. The online-generated acetaldehyde was subsequently undergoing aldol condensation to accelerate the formation of C<sub>4</sub> aldehydes, which, as the intermediates, were stabilized over Ca deficiency sites on the hydroxyapatite surface. The enriched C<sub>4</sub> aldehyde intermediates are further coupled with C<sub>2</sub>, C<sub>4</sub>, or C<sub>6</sub> aldehydes at the basic sites to produce longer-chain aldehydes (C ≥ 6), which are subsequently hydrogenated to form C<sub>6–12</sub> alcohols. Noticeably, compared to the original hydroxyapatite, the Ca-deficient hydroxyapatite showed enhanced density of basic sites, about two times higher. Hence, this catalyst remarkably boosted the yield of C<sub>6–12</sub> alcohols from ethanol upgrading. This work provides a strategy for the selective conversion of ethanol to C<sub>6–12</sub> alcohols.</p>\",\"PeriodicalId\":9,\"journal\":{\"name\":\"ACS Catalysis \",\"volume\":\"15 10\",\"pages\":\"8599–8610 8599–8610\"},\"PeriodicalIF\":13.1000,\"publicationDate\":\"2025-05-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Catalysis \",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acscatal.5c01449\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acscatal.5c01449","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Boosting C6–12 Higher Alcohols Yield from Ethanol Upgrading over Ca-Deficient Mesoporous Hydroxyapatite through Intermediates Enrichment of C4 Aldehyde
Ethanol upgrading to C6–12 alcohols offers a green pathway to high-valued chemicals. Achieving high yields of C6–12 alcohols remains challenging due to the complexity of the ethanol reaction network. Here, we report an efficient conversion of ethanol to C6–12 alcohols using Ca-deficient mesoporous hydroxyapatite as the catalyst, which was prepared from the reaction of NH3 and PO43–. The yield of C6–12 alcohols reached 34.5% with a selectivity of 59.3% at 325 °C and 0.1 MPa, exhibiting a high ethanol upgrading performance. Ethanol adsorption kinetics and ethanol-TPD-DRIFT results revealed that the ethanol diffusional time constant of the enlarged pore of the hydroxyapatite increased by 2.01 folds of the original hydroxyapatite, thereby facilitating the access of ethanol molecules to active sites, which was beneficial for ethanol dehydrogenation. The online-generated acetaldehyde was subsequently undergoing aldol condensation to accelerate the formation of C4 aldehydes, which, as the intermediates, were stabilized over Ca deficiency sites on the hydroxyapatite surface. The enriched C4 aldehyde intermediates are further coupled with C2, C4, or C6 aldehydes at the basic sites to produce longer-chain aldehydes (C ≥ 6), which are subsequently hydrogenated to form C6–12 alcohols. Noticeably, compared to the original hydroxyapatite, the Ca-deficient hydroxyapatite showed enhanced density of basic sites, about two times higher. Hence, this catalyst remarkably boosted the yield of C6–12 alcohols from ethanol upgrading. This work provides a strategy for the selective conversion of ethanol to C6–12 alcohols.
期刊介绍:
ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels.
The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.