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

IF 13.1 1区 化学 Q1 CHEMISTRY, PHYSICAL
Jia Wang, Wen-Cui Li, Andi Di, Li-Dong Zhao, Danhui Sun, Lei He and An-Hui Lu*, 
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引用次数: 0

摘要

乙醇升级为C6-12醇提供了一条高价值化学品的绿色途径。由于乙醇反应网络的复杂性,实现C6-12醇的高收率仍然具有挑战性。本文报道了以NH3和PO43 -反应制备的缺钙介孔羟基磷灰石为催化剂,将乙醇高效转化为C6-12醇。在325℃、0.1 MPa条件下,C6-12醇的收率为34.5%,选择性为59.3%,具有良好的乙醇升级性能。乙醇吸附动力学和乙醇- tpd - drift结果表明,羟基磷灰石扩孔后乙醇扩散时间常数比原羟基磷灰石增大2.01倍,有利于乙醇分子接近活性位点,有利于乙醇脱氢。在线生成的乙醛随后进行醛醇缩合,以加速C4醛的形成,C4醛作为中间体,在羟基磷灰石表面的缺钙位点上稳定下来。富集的C4醛中间体进一步在碱性位点与C2、C4或C6醛偶联,生成长链醛(C≥6),随后加氢生成C6 - 12醇。值得注意的是,与原始羟基磷灰石相比,缺钙羟基磷灰石的碱性位点密度增加了约两倍。因此,该催化剂显著提高了乙醇精制过程中C6-12醇的收率。这项工作为乙醇选择性转化为C6-12醇提供了一种策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Boosting C6–12 Higher Alcohols Yield from Ethanol Upgrading over Ca-Deficient Mesoporous Hydroxyapatite through Intermediates Enrichment of C4 Aldehyde

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.

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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
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.
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