多组分Pt/ c -沸石催化下高效选择性甘油电解乳酸和氢气的研究

IF 4.9 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY JPhys Materials Pub Date : 2023-11-09 DOI:10.1088/2515-7639/ad0561
Muhammad Aslam, Miriam Navlani-García, Diego Cazorla-Amorós, Hui Luo
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引用次数: 0

摘要

摘要在各种生产燃料和化学品的电化学反应中,甘油电解制氢和乳酸的反应受到了广泛的关注。然而,研究表明,基准铂基催化剂在选择性催化甘油转化为乳酸方面存在不足,导致乳酸产率较低。本文报道了用阴离子交换膜电极组合电解槽电解甘油的研究。对质量输运、温度、电流密度和KOH浓度等反应条件进行了优化,其中温度对反应速率和热力学有显著影响。在优化条件下,开发并测试了多组分Pt/C-沸石电催化剂体系(Pt/C- cbv600),该体系可将乳酸选择性从单独Pt/C时的33.8%提高到57.3%。虽然具体机理有待进一步研究,但我们假设具有丰富Lewis酸表面位点的CBV600沸石可以有效结合二羟基丙酮中间体,并驱动反应多相生成丙酮醛,这是形成乳酸的关键步骤。
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Efficient and selective glycerol electrolysis for the co-production of lactic acid and hydrogen with multi-component Pt/C-zeolite catalyst
Abstract Among various electrochemical reactions to produce fuels and chemicals, glycerol electrolysis to co-produce hydrogen and lactic acid has received great attention. However, studies have shown the benchmark Pt based catalysts are insufficient in selectively catalysing the glycerol to lactic acid transformation, resulting in a low yield of lactic acid. Here we report a study on glycerol electrolysis with anion-exchange membrane electrode assembly electrolyser. The reaction conditions including mass transport, temperature, current density and KOH concentration were optimised, among which temperature played a significant role in facilitating the reaction rate and thermodynamics. With the optimised condition a multicomponent Pt/C-zeolite electrocatalyst system (Pt/C-CBV600) was developed and tested, which is capable to increase the lactic acid selectivity to 57.3% from the 33.8% with standalone Pt/C. Although the detailed mechanism required further investigation, it is hypothesised that the CBV600 zeolite with abundant Lewis acid surface sites can effectively bind the dihydroxyacetone intermediate, and drive the reaction towards pyruvaldehyde heterogeneously, the key step to form lactic acid.
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来源期刊
JPhys Materials
JPhys Materials Physics and Astronomy-Condensed Matter Physics
CiteScore
10.30
自引率
2.10%
发文量
40
审稿时长
12 weeks
期刊最新文献
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