Small Au Nanoparticles Supported on MCM-41 Containing a Surfactant

被引:8
作者
Mokhonoana, Malose P. [1 ,2 ]
Coville, Neil J. [2 ]
Datye, Abhaya K. [3 ]
机构
[1] Univ Limpopo, Dept Chem, Sch Phys & Mineral Sci, ZA-0727 Sovenga, Polokwane, South Africa
[2] Univ Witwatersrand, Sch Chem, Inst Mol Sci, ZA-2050 Johannesburg, South Africa
[3] Univ New Mexico, Ctr Microengineered Mat, Dept Chem & Nucl Engn, Albuquerque, NM 87131 USA
关键词
Modified deposition-precipitation; As-synthesized Si-MCM-41; Gold nanoparticles; Surface migration; Coulombic interactions; LOW-TEMPERATURE OXIDATION; CO OXIDATION; GOLD NANOPARTICLES; CATALYTIC-ACTIVITY; PARTICLES; TIO2;
D O I
10.1007/s10562-010-0300-9
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
Gold nanoparticles (AuNPs) have been incorporated into undoped Si-MCM-41 by direct one-pot and post-synthesis approaches. Through a "modified deposition-precipitation'' (mDP) method, whereby ethylenediamine served as both a base and complexing agent for the Au(III) species, Au nanoparticles have been prepared exclusively inside the pore channels of Si-MCM-41 materials. The method exploits Coulombic interactions between the occluded cationic surfactant template and the anionic [AuCl4](-) to yield a controlled distribution and in-pore generation of AuNPs, i.e., DP of the Au precursor was aided by electrostatics. This method is simple and yields well-dispersed gold nanoparticles (AuNPs). The nanoparticles inside the matrix were seen to aggregate and migrate to the surface upon calcination at 500 degrees C, but showed a narrow Au particle size distribution. The nanocomposite materials synthesized in this study exhibited catalytic activity for the CO oxidation reaction, with CO conversion of <100% even at temperatures as high as 500 degrees C.
引用
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页码:1 / 9
页数:9
相关论文
共 48 条
[1]   Kinetics of CO Oxidation Catalyzed by Supported Gold: A Tabular Summary of the Literature [J].
Aguilar-Guerrero, Veronica ;
Gates, Bruce C. .
CATALYSIS LETTERS, 2009, 130 (1-2) :108-120
[2]   A NEW FAMILY OF MESOPOROUS MOLECULAR-SIEVES PREPARED WITH LIQUID-CRYSTAL TEMPLATES [J].
BECK, JS ;
VARTULI, JC ;
ROTH, WJ ;
LEONOWICZ, ME ;
KRESGE, CT ;
SCHMITT, KD ;
CHU, CTW ;
OLSON, DH ;
SHEPPARD, EW ;
MCCULLEN, SB ;
HIGGINS, JB ;
SCHLENKER, JL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (27) :10834-10843
[3]   THE REACTION OF GOLD(III) WITH SOME BIDENTATE COORDINATING GROUPS [J].
BLOCK, BP ;
BAILAR, JC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1951, 73 (10) :4722-4725
[4]  
Bond G.C., 2006, CATALYSIS GOLD, DOI 10.1007/bf03215560
[5]   Status of catalysis by gold following an AURICAT Workshop [J].
Bond, GC ;
Thompson, DT .
APPLIED CATALYSIS A-GENERAL, 2006, 302 (01) :1-4
[6]   Gold-catalysed oxidation of carbon monoxide [J].
Bond, GC ;
Thompson, DT .
GOLD BULLETIN, 2000, 33 (02) :41-51
[7]   Catalysis by gold [J].
Bond, GC ;
Thompson, DT .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1999, 41 (3-4) :319-388
[8]   Nanoparticles made in mesoporous solids [J].
Bronstein, LM .
COLLOID CHEMISTRY 1, 2003, 226 :55-89
[9]   Gold-organic-inorganic high-surface-area materials as precursors of highly active catalysts [J].
Budroni, Gerolamo ;
Corma, Avelino .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (20) :3328-3331
[10]   CO oxidation over gold nanocatalyst confined in mesoporous silica [J].
Chi, YS ;
Lin, HP ;
Mou, CY .
APPLIED CATALYSIS A-GENERAL, 2005, 284 (1-2) :199-206