Effect of polymeric stabilizers on Fischer-Tropsch synthesis catalyzed by cobalt nanoparticles supported on TiO2

被引:9
作者
Delgado, Jorge A. [1 ]
Claver, Carmen [1 ,2 ]
Castillon, Sergio [3 ]
Curulla-Ferre, Daniel [4 ]
Ordomsky, Vitaly V. [5 ]
Godard, Cyril [2 ]
机构
[1] Ctr Tecnol Quim, Tarragona 43007, Spain
[2] Univ Rovira & Virgili, Dept Quim Fis & Inorgan, C Marcelli Domingo S-N, E-43007 Tarragona, Spain
[3] Univ Rovira & Virgili, Dept Quim Analit & Organ, E-43007 Tarragona, Spain
[4] Total Res & Technol Feluy, B-7181 Seneffe, Belgium
[5] USTL ENSCL EC Lille, Unite Catalyse & Chim Solide, F-59655 Villeneuve Dascq, France
关键词
Fischer-Tropsch synthesis; Cobalt nanoparticles; Polymeric stabilizers; Sodium borohydride; BOROHYDRIDE REDUCTION; MODEL CATALYSTS; HYDROGENATION; SELECTIVITY; RUTHENIUM; CO; NANOCATALYSTS; NANOCRYSTALS; NANOSCALE; CO/TIO2;
D O I
10.1016/j.molcata.2016.02.029
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 series of colloidal cobalt nanoparticles of ca. 2.6 nm stabilized by several polymeric stabilizers were synthesized in water using sodium borohydride as reducing agent and subsequently immobilized on TiO2. Both colloidal and TiO2 supported NPs were characterized by TEM, HRTEM, XRD, XPS, TGA and ICP techniques and the catalytic performance of the supported NPs evaluated in the Fischer-Tropsch synthesis. Important differences in terms of activity were observed depending on the polymeric stabilizers used for the synthesis of the CoNPs. These differences were correlated with the catalyst reducibility, the presence of polymer stabilizer and boron and the reduction degree at the metal surface. From the tested catalysts, the NPs prepared in the presence of poly(2-ethyl-2-oxazoline) as stabilizer resulted to be the most active of the series, which was correlated with the higher reducibility of this catalyst. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:43 / 52
页数:10
相关论文
共 47 条
[1]   Boron Compounds as Stabilizers of a Complex Microstructure in a Co-B-based Catalyst for NaBH4 Hydrolysis [J].
Arzac, G. M. ;
Rojas, T. C. ;
Fernandez, A. .
CHEMCATCHEM, 2011, 3 (08) :1305-1313
[2]  
Bartholomew C.H., 1991, Studies in Surface Science and Catalysis, V64, P158
[3]   De Novo Design of Nanostructured Iron-Cobalt Fischer-Tropsch Catalysts [J].
Calderone, V. Roberto ;
Shiju, N. Raveendran ;
Curulla-Ferre, Daniel ;
Chambrey, Stephane ;
Khodakov, Andrei ;
Rose, Amadeus ;
Thiessen, Johannes ;
Jess, Andreas ;
Rothenberg, Gadi .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2013, 52 (16) :4397-4401
[4]   Nanoscaled Metal Borides and Phosphides: Recent Developments and Perspectives [J].
Carenco, Sophie ;
Portehault, David ;
Boissiere, Cedric ;
Mezailles, Nicolas ;
Sanchez, Clement .
CHEMICAL REVIEWS, 2013, 113 (10) :7981-8065
[5]   Size controlled synthesis of Co nanoparticles by combination of organic solvent and surfactant [J].
Chen, Yong ;
Liew, Kong Yong ;
Li, Jinlin .
APPLIED SURFACE SCIENCE, 2009, 255 (07) :4039-4044
[6]   Ordered Mesoporous Carbon Supported Colloidal Pd Nanoparticle Based Model Catalysts for Suzuki Coupling Reactions: Impact of Organic Capping Agents [J].
Choi, Ha Rim ;
Woo, Hyunje ;
Jang, Seongwan ;
Cheon, Jae Young ;
Kim, Chungho ;
Park, Jongnam ;
Park, Kang Hyun ;
Joo, Sang Hoon .
CHEMCATCHEM, 2012, 4 (10) :1587-1594
[7]   Studies on the Continuous Precipitation of Silver Nanoparticles [J].
Chou, Kan-Sen ;
Chang, Yu-Chun ;
Chiu, Lien-Hua .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2012, 51 (13) :4905-4910
[8]  
Dancuart L.P., 2007, FISCHER TROPSCH SYNT, P379
[9]   Fischer-Tropsch synthesis catalysed by small TiO2 supported cobalt nanoparticles prepared by sodium borohydride reduction [J].
Delgado, Jorge A. ;
Claver, Carmen ;
Castillon, Sergio ;
Curulla-Ferre, Daniel ;
Ordomsky, Vitaly V. ;
Godard, Cyril .
APPLIED CATALYSIS A-GENERAL, 2016, 513 :39-46
[10]   Effect of pH on catalyst activity and selectivity in the aqueous Fischer-Tropsch synthesis catalyzed by cobalt nanoparticles [J].
Delgado, Jorge A. ;
Castilion, Sergio ;
Curulla-Ferre, Daniel ;
Claver, Carmen ;
Godard, Cyril .
CATALYSIS COMMUNICATIONS, 2015, 71 :88-92