二苯并噻吩
多金属氧酸盐
烟气脱硫
兴奋剂
金属有机骨架
稀土元素
氧化磷酸化
化学
硫黄
无机化学
稀土
材料科学
有机化学
矿物学
催化作用
吸附
生物化学
光电子学
作者
Mingyu Liao,Yuanjie Xiao,Xiaolin Pi,Linfeng Zhang,Miaomiao Zheng,Mingnan Qu,Huadong Wu,Jia Guo
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2024-07-09
卷期号:38 (14): 12555-12568
标识
DOI:10.1021/acs.energyfuels.4c01125
摘要
By designing metal–organic frameworks (MOFs) doped with rare-earth elements, we can enhance catalytic activity and stability in a novel way. In the realm of oxidative desulfurization (ODS), polyoxometalate-ionic liquids have outstanding desulfurization performance. Herein, to create La-UiO-66 and Y-UiO-66, respectively, rare-earth elements (REs) of yttrium (Y) and lanthanum (La) were doped into the Zr-based metal–organic framework UiO-66. After that, the catalyst [C12mim]3PW12O40/RE-UiO-66 was prepared by supporting a type of polyoxometalate-ionic liquid [C12mim]3PW12O40 with a large specific surface area and stable structure on RE-UiO-66 (RE = La or Y). The catalyst was characterized and analyzed by XRD, FT-IR, SEM, and other methods. The ODS reaction of the dibenzothiophene model oil was conducted in the oxidative desulfurization experiment with H2O2 as the oxidant and [C12mim]3PW12O40/RE-UiO-66 as the catalyst, and the ideal reaction conditions were determined. Under the optimum reaction conditions (T = 60 °C, O/S = 5), due to the strength of electron transfer over the catalysts, the DBT removal efficiencies of [C12mim]3PW12O40/0.18La-UiO-66–25% and [C12mim]3PW12O40/0.09Y-UiO-66–25% were 100% in 40 min and 97% in 60 min, respectively. The desulfurization efficiency was maintained at 91% after 13 cycles with [C12mim]3PW12O40/0.18La-UiO-66–25% as a catalyst. In addition, a proposed reaction mechanism for the ODS reaction over this catalyst was presented.
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