Efficient and rapid removal of thiophene sulfides from fuel using zirconia-loaded phosphotungstic acid†

IF 3.9 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
RSC Advances Pub Date : 2025-05-19 DOI:10.1039/D5RA02041G
Rui Liang, Yu Hu, YuFang Ye and Qing Wang
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引用次数: 0

Abstract

In this study, a new type of composite was synthesized via the sol–gel method. The structure and properties of the composite were analyzed using X-ray diffraction, scanning electron microscopy, nitrogen isothermal adsorption and desorption tests, Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. Characterization results showed that phosphotungstic acid (PW12) was successfully loaded on zirconium dioxide (ZrO2). The oxidative desulfurization performance of 500 ppm dibenzothiophene (DBT) was studied with H2O2 as the oxidant and xPW12/ZrO2 as the catalyst. Under optimal conditions (T = 60 °C, O/S = 2 and m = 0.03 g), the desulfurization rate reached 97.85% within 20 min, and the activity did not decrease significantly after 8 cycles. The kinetics of the reaction was studied at different temperatures. Results showed that the oxidation rate conforms to quasi-first-order kinetics and the apparent activation energy is 23.32 kJ mol−1. Therefore, the composite material is expected to be a catalyst for oxidative desulfurization.

利用负载氧化锆的磷钨酸快速高效地去除燃料中的噻吩硫化物
本研究采用溶胶-凝胶法合成了一种新型复合材料。采用x射线衍射、扫描电镜、氮气等温吸附和脱附、傅里叶变换红外光谱和x射线光电子能谱分析了复合材料的结构和性能。表征结果表明,磷钨酸(PW12)成功负载在二氧化锆(ZrO2)上。以H2O2为氧化剂,xPW12/ZrO2为催化剂,研究了500 ppm二苯并噻吩(DBT)的氧化脱硫性能。在最佳条件下(T = 60℃,O/S = 2, m = 0.03 g), 20 min内脱硫率达到97.85%,8次循环后活性没有明显下降。研究了不同温度下的反应动力学。结果表明,氧化反应符合准一级动力学,表观活化能为23.32 kJ mol−1。因此,该复合材料有望成为氧化脱硫的催化剂。
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来源期刊
RSC Advances
RSC Advances chemical sciences-
CiteScore
7.50
自引率
2.60%
发文量
3116
审稿时长
1.6 months
期刊介绍: An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.
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