Enhancing the Green Synthesis of Glycerol Carbonate: Carboxylation of Glycerol with CO2 Catalyzed by Metal Nanoparticles Encapsulated in Cerium Metal–Organic Frameworks

催化作用 对苯二甲酸 金属有机骨架 甘油 胶体金 纳米颗粒 羧化 金属 材料科学 碳酸盐 化学 无机化学 化学工程 核化学 有机化学 纳米技术 吸附 聚酯纤维 工程类
作者
Simon Lukato,Michał Wójcik,Agnieszka Krogul-Sobczak,Grzegorz Litwinienko
出处
期刊:Nanomaterials [Multidisciplinary Digital Publishing Institute]
卷期号:14 (8): 650-650
标识
DOI:10.3390/nano14080650
摘要

The reaction of glycerol with CO2 to produce glycerol carbonate was performed successfully in the presence of gold nanoparticles (AuNPs) supported by a metal–organic framework (MOF) constructed from mixed carboxylate (terephthalic acid and 1,3,5-benzenetricarboxylic acid). The most efficient were two AuNPs@MOF catalysts prepared from pre-synthesized MOF impregnated with Au3+ salt and subsequently reduced to AuNPs using H2 (catalyst 4%Au(H2)@MOF1) or reduced with NaBH4 (catalyst 4%Au@PEI-MOF1). Compared to existing catalysts, AuNPs@MOFs require simple preparation and operate under mild and sustainable conditions, i.e., a much lower temperature and the lowest CO2 overpressure ever reported, with MgCO3 having been found to be the optimal dehydrating agent. Although the yield of the process is still not competitive with previously developed systems, the most promising advantage is the highest TOF (78 h−1) ever reported for this reaction. The optimal parameters observed for AuNPs were also tested on AgNPs and CuNPs with promising results, suggesting their great potential for industrial application. The catalysts were characterized by XRD, TEM, SEM-EDS, ICP-MS, XPS, and porosity measurements, confirming that AuNPs are present in low concentration, uniformly distributed, and confined to the cavities of the MOF.
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