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Deep oxidative desulfurization of diesel fuels using homogeneous and SBA-15-supported peroxophosphotungstate catalysts

机译:使用均相和SBA-15负载的过氧磷钨酸盐催化剂对柴油进行深度氧化脱硫

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摘要

A combination of catalytic oxidation and extraction was used for the desulfurization of a model diesel containing benzothiophene, dibenzothiophene and 4,6-dimethyldibenzothiophene, or a real diesel sample with a sulfur content of 2300 ppm. The catalysts used were the soluble peroxo compound (nBu(4)N)(3){PO4[WO(O-2)(2)](4)} (PW4) and a supported material denoted as PW4@TMA-SBA-15 that was prepared by immobilization of PW4 in an ordered mesoporous silica (SBA-15) derivatized with propyltrimethylammonium groups (TMA). The supported catalyst was characterized by FT-IR, FT-Raman, P-31 and C-13 MAS NMR spectroscopies, powder X-ray diffraction and scanning electron microscopy. Under optimized conditions (H2O2/S molar ratio = 7, 70 degrees C, acetonitrile as extraction solvent), both catalysts led to complete desulfurization of the model diesel within a reaction time of 2 h. The desulfurization systems could be recycled 10 times with only a slight decrease in performance being observed between the 9th and 10th oxidative desulfurization cycles. Application of the PW4 system to the real diesel led to an outstanding desulfurization efficiency of 89% after a reaction time of 2 h.
机译:催化氧化和萃取的组合用于含苯并噻吩,二苯并噻吩和4,6-二甲基二苯并噻吩的模型柴油或硫含量为2300 ppm的真实柴油样品的脱硫。所使用的催化剂是可溶性​​过氧化合物(nBu(4)N)(3){PO4 [WO(O-2)(2)](4)}(PW4)和表示为PW4 @ TMA-SBA-图15是通过将PW4固定在用丙基三甲基铵基团(TMA)衍生的有序介孔二氧化硅(SBA-15)中制备的。通过FT-IR,FT-Raman,P-31和C-13 MAS NMR光谱,粉末X射线衍射和扫描电子显微镜对负载的催化剂进行了表征。在优化的条件下(H2O2 / S摩尔比= 7,70摄氏度,乙腈作为萃取溶剂),两种催化剂均能在2 h的反应时间内使模型柴油完全脱硫。脱硫系统可以循环使用10次,而在第9和第10个氧化脱硫循环之间,观察到的性能仅略有下降。将PW4系统应用于实际柴油后,反应2小时后,脱硫效率达到89%。

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