期刊
CATALYSIS SCIENCE & TECHNOLOGY
卷 7, 期 4, 页码 6112-6123出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7cy02008b
关键词
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资金
- National Natural Science Foundation of China [21273076, 21373089]
- Open Research Fund of Top Key Discipline of Chemistry in Zhejiang Provincial Colleges
- Key Laboratory of the Ministry of Education for Catalysis Materials (Zhejiang Normal University) [ZJHX2013]
- Shanghai Leading Academic Discipline Project [B409]
TiO2 was coated onto mesoporous silica SBA-15 by hydrolysis of tetrabutyl titanate to prepare 15 wt% TiO2@SBA-15 composites (15TS). The 15TS composites retain the mesostructure of the SBA-15 host, and TiO2 was highly dispersed and uniformly coated. 5 wt% Pt nanoparticles supported on 15TS were employed for liquid-phase selective hydrogenation of cinnamaldehyde (CAL) to cinnamyl alcohol (COL). Compared with the Pt catalyst supported on pristine SBA-15, the Pt/15TS catalyst afforded higher activity and selectivity to COL. Furthermore, the modification of the Pt/15TS catalyst by FeOx can greatly improve the activity and selectivity to COL. As a result, the Pt-FeOx/15TS catalyst displayed excellent selectivity to COL (around 84.5%) at nearly complete CAL conversion. Of particular note is that further calcination of the Pt-FeOx/15TS catalyst precursor in air at 773 K before reduction would greatly enhance the catalytic performance. Consequently, the TOF reached 3.06 s(-1) with a selectivity to COL of 86.4% over the Pt-FeOx/15TS-773 catalyst. Moreover, the Pt-FeOx/15TS-773 catalyst can also be reused about eight times without distinct loss in activity or selectivity. Based on characterization by XPS and H-2-TPR, the important promotion effect of FeOx and strong metal-support interaction played key roles in preferential adsorption and activation of C=O bonds in CAL.
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