Control of the thickness of mesoporous titania films for application in multiphase catalytic microreactors

被引:39
作者
Protasova, Lidia N. [1 ,2 ]
Rebrov, Evgeny V. [1 ]
Glazneva, Tatiana S. [2 ]
Berenguer-Murcia, Angel [3 ]
Ismagilov, Zinfer R. [2 ]
Schouten, Jaap C. [1 ]
机构
[1] Eindhoven Univ Technol, NL-5600 MB Eindhoven, Netherlands
[2] Boreskov Inst Catalysis, Novosibirsk 630090, Russia
[3] Univ Alicante, Dept Quim Inorgan, E-03080 Alicante, Spain
基金
俄罗斯基础研究基金会;
关键词
Mesoporous titania films; Au nanoparticles; Citral hydrogenation; GAS SHIFT REACTION; THIN-FILMS; MICROSTRUCTURED REACTORS; HYDROTHERMAL SYNTHESIS; SILICA FILMS; PHOTOCATALYTIC ACTIVITY; SINGLE-LAYER; TIO2; SUPPORT; HYDROGENATION;
D O I
10.1016/j.jcat.2009.07.013
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A new method of sol-gel polymer template synthesis of mesoporous catalytic thin films has been proposed which allows controlling the chemical nature of the film, the porosity, thickness and loading with an active species. The mesoporous films with a long-order structure can be obtained in a narrow range of surfactant-to-metal precursor molar ratios from 0.006 to 0.009. The catalytic film thickness was varied from 300 to 1000 nm while providing a uniform catalyst distribution with a desired catalyst loading (1 wt. % Au nanoparticles) throughout the film. The films were characterized by TEM, SEM, ethanol adsorption and contact angle measurements. The calcination of the as-synthesized films at 573 K reduced Ti4+ sites to Ti3+. A 300 nm thick Au-containing film showed an initial TOF of 1.4 s(-1) and a selectivity towards unsaturated alcohols as high as 90% in the hydrogenation of citral. Thicker films demonstrated a high selectivity towards the saturated aldehyde (above 55%) and a lower intrinsic catalytic activity (initial TOF of 0.7-0.9 s(-1)) in the absence of internal diffusion limitations. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:161 / 169
页数:9
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