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Cu Nanoparticles Inlaid Mesoporous Al2O3 As a High-Performance Bifunctional Catalyst for Ethanol Synthesis via Dimethyl Oxalate Hydrogenation

机译:铜纳米颗粒镶嵌介孔Al2O3作为草酸二甲酯加氢合成乙醇的高性能双功能催化剂

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摘要

Ethanol synthesis from syngas via dimethyl oxalate (DMO) hydrogenation is of crucial importance for environment- and energy-related applications. Herein, we designed the bifunctional Cu nanoparticle (NP) inlaid mesoporous Al2O3 catalyst and first applied it to ethanol synthesis with high efficiency. The catalyst was made based on the spatial restriction strategy by pinning the Cu NPs on mesoporous Al2O3 to conquer the sintering problem and facilitate the stability (>200 h at 270 °C), which has potential values in high-temperature and exothermic reactions. The plentiful pores, highly exposed and properly assembled Cu-acid sites, furnished the catalyst with high ethanol yield (~94.9%). A structure-sensitive behavior that the intrinsic activity increases with the decreasing NP size was discussed. It was attributed to the change in metal-acid interfacial sites, morphology, and electronic structure and balance of surface Cu~0-Cu~+ species. The mechanism for DMO hydrogenation to ethanol involving activation of C=O, C-O, and O-H bands was also proposed. As cleavage of these bonds is a versatile tool to utilize bioderived molecules (e.g., polyols), the bifunctional catalysts can also be applied to hydrogenolysis of C-O bonds or etherification of O-H groups to produce various chemicals.
机译:通过草酸二甲酯(DMO)加氢从合成气合成乙醇对于与环境和能源相关的应用至关重要。在这里,我们设计了双功能Cu纳米粒子(NP)镶嵌介孔Al2O3催化剂,并首先将其高效地应用于乙醇合成。该催化剂是基于空间限制策略而制得的,方法是将Cu NPs固定在介孔Al2O3上以克服烧结问题并促进稳定性(在270°C时> 200 h),这在高温和放热反应中具有潜在价值。大量的孔,高度暴露且正确组装的铜酸位点为催化剂提供了较高的乙醇收率(〜94.9%)。讨论了内在活性随NP尺寸减小而增加的结构敏感行为。归因于金属酸界面部位,形态,表面Cu〜0-Cu〜+种类的电子结构和平衡的变化。还提出了DMO加氢制乙醇的机制,涉及C = O,C-O和O-H谱带的活化。由于这些键的断裂是利用生物来源的分子(例如多元醇)的通用工具,因此双功能催化剂也可以用于C-O键的氢解或O-H基团的醚化以产生各种化学物质。

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