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Ultra-Deep Oxidative Desulfurization of Model Oil Catalyzed by In Situ Carbon-Supported Vanadium Oxides Using Cumene Hydroperoxide as Oxidant

机译:用原位碳支持的氧化钒催化的模型油的超深氧化脱硫化,使用液质过氧化物作为氧化剂

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摘要

A series of novel dispersed V2O5@Carbon composites, in which vanadium existed not only on the surface of carbon, but also in the matrix, were synthesized in situ from ammonium metava- nadate (NH4VO3) and ethylenediaminetetraacetic acid disodium salt dihydrate (EDTA-2Na). The structures and properties of prepared catalysts were characterized by diverse techniques. An efficient process for catalytic oxidative desulfurization with V2O5@Carbon and cumene hydroperoxide (CHP) was investi- gated. V2O5@Carbons is superior to the physically supported catalysts in reusability and stability. Results show that 99.8% sulfur in fuel can be removed and the catalyst can be recycled 7 times with no significant decrease in the desulfurization efficiency. A possible reaction mechanism is proposed, in which V(V)=O was oxidized to peroxo compounds (V(O)2) by CHP along with forming the 2-phenyl-2-propanol. The V(O)2 further cleaved to form electrophilic reactive VIV -O-O. species which could oxidize sulfur compounds to corresponding sulfones.
机译:一系列新颖的分散的V2O5@碳复合材料,其中不仅存在于碳表面,而且还存在于基质中,也从原位中合成了Metava-Nadate(NH4VO3)和乙基二苯甲酸二乙酸乙酸乙酸苯胺含量(Edta-edta-dihydrate(Edta-dihydrate)(乙二醇) )。制备的催化剂的结构和性能以各种技术为特征。投资了用V2O5@碳和Cumene氢过氧化物(CHP)进行催化氧化脱硫化的有效过程。 V2O5@Carbons在可重复使用和稳定性方面优于身体支持的催化剂。结果表明,燃料中的99.8%硫可以去除,催化剂可以回收7次,而脱硫效率没有显着降低。提出了一种可能的反应机制,其中V(V)= O通过CHP氧化为过氧化合物(V(O)2),并形成2-苯基-2-丙醇。 V(o)2进一步裂解以形成亲电反应性viv -o -O。可能氧化硫化合物的物种。

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