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用于将苯甲醇有氧氧化为苯甲酸苄酯的Au/VPO中金属-载体协同效应

Metal-Support Cooperative Effects in Au/VPO for the Aerobic Oxidation of Benzyl Alcohol to Benzyl Benzoate.

作者信息

Campisi Sebastiano, Ferri Michele, Chan-Thaw Carine E, Sanchez Trujillo Felipe J, Motta Davide, Tabanelli Tommaso, Dimitratos Nikolaos, Villa Alberto

机构信息

Università degli Studi di Milano, Dipartimento di Chimica, Via C. Golgi 19, 20133 Milano, Italy.

Institut pour la Maîtrise de l'Énergie⁻Université d'Antananarivo BP 566, 101 Antananarivo, Madagascar.

出版信息

Nanomaterials (Basel). 2019 Feb 20;9(2):299. doi: 10.3390/nano9020299.

Abstract

This paper studies the cooperative effect of Au nanoparticles deposited on vanadyl pyrophosphate oxide (VPO) in the liquid phase oxidation of benzyl alcohol. VPO was prepared using the classical method by thermally treating VOHPO₄·0.5H₂O precursor in reacting atmosphere at 420 °C for a period of 72 h. Au nanoparticles were deposited by incipient wetness method. The catalysts were characterized by means of XRD, TEM, XPS and Raman. The bulk VPO catalyst contains vanadyl pyrophosphate phase ((VO)₂P₂O₇), and a small amount of VOPO₄. The catalytic system exhibits a high activity in the base-free liquid phase oxidation of alcohols compared to Au on activated carbon, classic catalyst used for this type of reaction. Au/VPO showed a high peculiar selectivity to benzyl benzoate (76%), an important product used in the pharmaceutical and perfume industries. This behavior might be ascribed to the presence of strong acid sites of VPO, as determined by liquid phase titration. Stability tests performed on Au/VPO showed a deactivation of 10% after the first run, but a constant conversion along the following five cycles. This phenomenon can be attributed to the increase of mean Au particle size (from 19.1 to 23.4 nm) after recycling tests as well as the partial leaching of Au and V in the reaction media. Moreover, XRD evidenced a modification in the VPO structure with the partial formation of VOHPO₄·0.5H₂O phase.

摘要

本文研究了负载于焦磷酸氧钒(VPO)上的金纳米颗粒在苯甲醇液相氧化反应中的协同效应。VPO采用经典方法制备,即将VOHPO₄·0.5H₂O前驱体在反应气氛中于420℃热处理72小时。通过初湿浸渍法负载金纳米颗粒。采用XRD、TEM、XPS和拉曼光谱对催化剂进行了表征。块状VPO催化剂包含焦磷酸氧钒相((VO)₂P₂O₇)和少量VOPO₄。与用于此类反应的经典催化剂——活性炭负载的金相比,该催化体系在无碱醇类液相氧化反应中表现出高活性。Au/VPO对苯甲酸苄酯(76%)表现出高选择性,苯甲酸苄酯是制药和香料行业的重要产品。通过液相滴定测定,这种行为可能归因于VPO存在强酸位点。对Au/VPO进行的稳定性测试表明,首次运行后失活10%,但在随后的五个循环中转化率保持恒定。这种现象可归因于循环测试后金颗粒平均尺寸的增加(从19.1纳米增加到23.4纳米)以及反应介质中Au和V的部分浸出。此外,XRD证明VPO结构发生了变化,部分形成了VOHPO₄·0.5H₂O相。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa49/6410264/6305ecf2a6e6/nanomaterials-09-00299-g001.jpg

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