李钢

个人信息Personal Information

教授

博士生导师

硕士生导师

性别:男

毕业院校:大连理工大学

学位:博士

所在单位:化工学院

学科:工业催化. 能源化工. 物理化学

办公地点:西校区化工实验楼B525

联系方式:13940918701

电子邮箱:liganghg@dlut.edu.cn

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Mesoporous Titanium-Silicalite Zeolite Containing Organic Templates as a Bifunctional Catalyst for Cycloaddition of CO2 and Epoxides

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论文类型:期刊论文

发表时间:2018-07-04

发表刊物:ACS APPLIED MATERIALS & INTERFACES

收录刊物:PubMed、SCIE

卷号:10

期号:26

页面范围:22119-22129

ISSN号:1944-8244

关键字:mesoporous zeolites; organic templates; bifunctional catalyst; cycloaddition reaction; cyclic carbonate

摘要:Mesoporous TS-1 (MTS-1) containing organic templates tetrapropylammonium hydroxide (TPAOH) and polydiallyldimethylammonium chloride is synthesized and treated with different concentrations of hydrochloric acid aqueous solution. The as-synthesized MTS-1 are characterized using X-ray diffraction, Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy, transmission electron microscopy, UV-vis, C-13 cross-polarization/magic angle spinning (CP/MAS) NMR, thermogravimetry analysis, CO2-temperature-programmed desorption (TPD), N-2 adsorption-desorption, X-ray fluorescence, and elemental analysis. The results of C-13 CP/MAS NMR show that the structures of organic templates are retained after acid washing treatment. Not required to be removed by calcination, the organic templates embedded in MTS-1 can take the role of basic sites and activate carbon dioxide (CO2), which is confirmed by FT-IR. Moreover, the amount of acid sites and basic sites in the samples before and after acid treatment is characterized by modified Hammett indicator method and CO2-TPD, respectively. The results show that both the acidity and the basicity in the material are improved after acid washing. Thus, the sample after acid treatment contains two active sites: basic sites stemming from organic species and acid sites coming from framework Ti, which is beneficial to be used as a bifunctional catalyst in the cycloaddition reaction of CO2 and epoxides. It is highly active in the cycloaddition reaction, in which the conversion of epichlorohydrin (ECH) could reach 97.8% and the selectivity of cyclic carbonate is 98.0% under 1.6 MPa at 393 K for 6 h when acetonitrile is used as a solvent. Moreover, the kinetics of the cycloaddition reaction are studied using ECH as a substrate by varying the reaction parameters. More importantly, the organic-inorganic hybrid catalyst is reusable and stable against leaching of organic species in the cycloaddition reaction.