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负载于单分散UiO-66微晶内的钌纳米颗粒与多金属氧酸盐的协同催化作用用于提高乙酰丙酸甲酯制γ-戊内酯的效率

Synergistic Catalysis of Ruthenium Nanoparticles and Polyoxometalate Integrated Within Single UiO-66 Microcrystals for Boosting the Efficiency of Methyl Levulinate to γ-Valerolactone.

作者信息

Cai Xiaoxiong, Xu Qionghao, Tu Gaomei, Fu Yanghe, Zhang Fumin, Zhu Weidong

机构信息

Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, Institute of Physical Chemistry, Zhejiang Normal University, Jinhua, China.

出版信息

Front Chem. 2019 Feb 1;7:42. doi: 10.3389/fchem.2019.00042. eCollection 2019.

DOI:10.3389/fchem.2019.00042
PMID:30775365
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6367244/
Abstract

The synthesis of heterogeneous cooperative catalysts in which two or more catalytically active components are spatially separated within a single material has generated considerable research efforts. The multiple functionalities of catalysts can significantly improve the efficiency of existing organic chemical transformations. Herein, we introduce ruthenium (Ru) nanoparticles (NPs) on the surfaces of a metal-organic framework pre-encapsulated with polyoxometalate silicotungstic acid (SiW) UiO-66 (University of Oslo [UiO]) and prepared a 2.0% Ru/11.7% SiW@UiO-66 porous hybrid using the impregnation method. The close synergistic effect of metal Ru NPs, SiW, and UiO-66 endow 2.0% Ru/11.7% SiW@UiO-66 with increased activity and stability for complete methyl levulinate (ML) conversion and exclusive γ-valerolactone (GVL) selectivity at mild conditions of 80°C and at a H pressure of 0.5 MPa. Effectively, this serves as a model reaction for the upgrading of biomass and outperforms the performances of the constituent parts and that of the physical mixture (SiW + Ru/UiO-66). The highly dispersed Ru NPs act as active centers for hydrogenation, while the SiW molecules possess Brønsted acidic sites that cooperatively promote the subsequent lactonization of MHV to generate GVL, and the UiO-66 crystal accelerates the mass transportation facilitated by its own porous structure with a large surface area.

摘要

在单一材料中使两种或更多种催化活性组分在空间上分离的多相协同催化剂的合成已经引发了大量的研究工作。催化剂的多种功能可以显著提高现有有机化学转化的效率。在此,我们在预先封装有聚金属氧酸盐硅钨酸(SiW)的金属有机框架UiO-66(奥斯陆大学[UiO])的表面引入钌(Ru)纳米颗粒(NPs),并使用浸渍法制备了2.0% Ru/11.7% SiW@UiO-66多孔杂化物。金属Ru NPs、SiW和UiO-66之间紧密的协同效应赋予2.0% Ru/11.7% SiW@UiO-66在80°C温和条件和0.5 MPa氢气压力下,对乙酰丙酸甲酯(ML)完全转化和对γ-戊内酯(GVL)具有唯一选择性的活性和稳定性增强。有效地,这作为生物质升级的模型反应,并且优于各组成部分以及物理混合物(SiW + Ru/UiO-66)的性能。高度分散的Ru NPs充当氢化的活性中心,而SiW分子具有布朗斯台德酸性位点,协同促进MHV随后的内酯化以生成GVL,并且UiO-66晶体通过其自身具有大表面积的多孔结构加速传质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dae/6367244/ad61ddeb1192/fchem-07-00042-g0011.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dae/6367244/8e9f41366228/fchem-07-00042-g0003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dae/6367244/507e930f689e/fchem-07-00042-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dae/6367244/dea810486c71/fchem-07-00042-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dae/6367244/e1955dbb141b/fchem-07-00042-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dae/6367244/b5f0743505cd/fchem-07-00042-g0008.jpg
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