Au nanoparticles confined in hybrid shells of silica nanospheres for solvent-free aerobic cyclohexane oxidation

被引:20
作者
Chen, Lifang [1 ]
Zhou, Yuanyuan [2 ]
Gui, Zhenyou [1 ]
Cheng, Hongye [1 ]
Qi, Zhiwen [1 ]
机构
[1] East China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
[2] Huazhong Agr Univ, Coll Sci, State Key Lab Agr Microbiol, Wuhan 430070, Peoples R China
基金
中国国家自然科学基金;
关键词
RAMAN-SPECTROSCOPY; MESOPOROUS SILICA; CATALYZED OXIDATION; GOLD NANOPARTICLES; LIQUID-PHASE; SURFACE; PRECIPITATION; NANOCRYSTALS; ADSORPTION; MECHANISM;
D O I
10.1007/s10853-017-0954-4
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Gold nanoparticles (NPs) confined in hybrid shells of organic linker-assisted silica nanospheres (GOS) have been prepared through a facile approach using organic amino functional groups covalently bound to shells of silica nanospheres for anchoring AuCl4 (-). Due to the hydrolysis of urea, the gold precursor was in situ reduced in the hybrid shells of silica nanospheres under desired alkaline and temperature conditions. Organic functional groups (-SiCH2CH2CH2NHCH2CH2NH2) were introduced into shells of silica nanospheres via a co-condensation of tetraethyl orthosilicate and 3-(2-aminoethylamino)propyl dimethoxymethylsilane. The results indicate that Au NPs with < 2 nm diameters were highly dispersed and well confined in the hybrid shells of silica nanospheres through the anchorage of organic functional groups under condensation process. The obtained GOS catalyst exhibited efficient catalytic activity for solvent-free catalytic oxidation of cyclohexane with 94.8% selectivity to cyclohexanone and cyclohexanol (KA oil) and adipic acid under 150 A degrees C, 1.5 MPa O-2 for 3 h.
引用
收藏
页码:7186 / 7198
页数:13
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