Synthesis of cobalt-iron bimetallic nanocrystals supported on mesoporous silica using different templates

被引:12
作者
Braganca, L. F. F. P. G. [2 ]
Avilez, Roberto R. [3 ]
Pais de Silva, Maria Isabel [1 ]
机构
[1] Pontificia Univ Catolica Rio de Janeiro, Dept Quim, BR-22453900 Rio De Janeiro, Brazil
[2] Univ Fed Fluminense, Dept Engn Quim & Petr, Rio De Janeiro, Brazil
[3] Pontificia Univ Catolica Rio de Janeiro, Dept Met & Mat, BR-22453900 Rio De Janeiro, Brazil
关键词
Hexagonal mesoporous silica; Co/HMS; Fe/HMS; Bimetallic CoFe/HMS; FISCHER-TROPSCH SYNTHESIS; HMS MOLECULAR-SIEVES; CATALYSTS; CO; REDUCIBILITY; CARBON; PROMOTER; DISPERSION; REDUCTION; COPOLYMER;
D O I
10.1016/j.colsurfa.2010.01.025
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
CoFe bimetallic samples containing 25 wt% total of metal content were prepared by incipient wetness impregnation of cobalt nitrate and iron nitrate salts over hexagonal mesoporous silica (HMS). A series of HMS silicas have been prepared by a neutral assembly pathway using two types of structure director: dodecylamine (DDA) and tetradecylamine (TDA). The effect of different templates in the formation of HMS mesoporous silica and bimetallic CoFe supported samples has been investigated and characterized by N-2 physisorption, X-ray diffraction (XRD), temperature programmed reduction (TPR), hydrogen chemisorption, thermogravimetric (TGA) and differential thermal (DTA) analyses. The amount of incorporated metal was estimated by atomic absorption spectroscopy (AAS). Also, a series of supported monometallic cobalt/iron samples were synthesized and compared to bimetallic ones. The textural properties revealed a lower percentage decrease in BET area and total pore volume for the CoFe/HMS (DDA) sample. XRD results showed alpha-Fe2O3 phase formation and higher Co3O4/CoFe2O4 crystallite sizes for CoFe/HMS (TDA) sample. The latter also presented lower reduction temperatures and a slightly lower dispersion (%) compared to CoFe/HMS (DDA). (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:79 / 87
页数:9
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