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

电子邮箱:liganghg@dlut.edu.cn

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Deep oxidative desulfurization catalyzed by Ti-based metal-organic frameworks

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论文类型:期刊论文

发表时间:2018-05-01

发表刊物:FUEL

收录刊物:SCIE、EI

卷号:219

页面范围:103-110

ISSN号:0016-2361

关键字:Ti-based MOFs; Extractive catalytic oxidative desulfurization; Methanol; Hydrogen peroxide

摘要:Ti-based metal-organic frameworks (MOFs) MIL-125 and NH2-MIL-125 were synthesized by the solvothermal method and characterized by X-ray powder diffraction (XRD), Fourier transform infrared (FT-IR), scanning electron microscopy (SEM) and diffuse reflectance UV-vis spectroscopy (DR/UV-vis). The crystal sizes of MIL-125 were regulated by changing the concentration of Ti ions in the synthesis system. Catalytic properties of MIL-125 and NH2-MIL-125 were evaluated in extractive and catalytic oxidative desulfurization (ECODS) by using H2O2 as the oxidant. In the ECODS system, the oxidative removal rate using MIL-125 or NH2-MIL-125 increases in the order as 4, 6-dimethyldibenzothiophene (4,6-DMDBT) < thiophene (Th) < benzothiophene (BT) < dibenzothiophene (DBT). The presence of -NH2 group in NH2-MIL-125 prevents sulfur compounds from contacting with Ti sites in a certain extent, resulting in the lower removal rate of NH2-MIL-125 comparing with that of MIL-125 in most cases. MIL-125 with smaller crystal size presents lower sulfides removal rate, which indicates that the active titanium species in MIL-125 is the decisive factor to affecting ODS. Both NH2-MIL-125 and MIL-125 show high stability in the presence of methanol and still maintain the integrity of the structure after being recycled five times. Methanol can inhibit H2O2 from damaging Ti-based MOFs and extract the oxidized products, which is beneficial to the ODS. While in the absence of extractant such as methanol, tert-butyl hydroperoxide (TBHP) is the optimal oxidant.