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Activity of CoMo/MSA catalysts in benzothiophene hydrodesulfurization, cumene cracking and cyclohexene isomerization

机译:苯并噻吩加氢硫化,异丙苯裂解和环己烯异构中的COMO / MSA催化剂的活性

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The mesoporous silica-alumina (SA) was modified by acid leaching and studied as an alternative support for Mo and CoMo catalysts for hydrodesulfurization (HDS) of benzothiophene. The supports were characterized by N2 adsorption, XRD, 27AL MAS NMR, electron microscopy (SEM, HRTEM) and their acidity were compared in cyclohexene isomerization and cumene cracking. The composition of catalysts were determined by ICP. Progressive leaching of the parent SA containing 52 wt.% Al2O3 (SA52) led to decrease of Al2O3 content (33 and 19 wt.% in MSA33 and MSA19 support, respectively). This decrease was accompanied with an increase of the BET surface area and exposition of strong acidity. The acid leaching positively affected the activities of the sulfided CoMo catalysts in the benzothiophene HDS, which were slightly above the activity of an industrial reference CoMo catalyst supported on gamma-Al2O3.
机译:中孔二氧化硅 - 氧化铝(SA)通过酸浸出改性,并作为苯并噻吩的加氢脱硫(HDS)的Mo和Como催化剂的替代载体进行研究。通过N 2吸附,XRD,27AL MAS NMR,电子显微镜(SEM,HRTEM)和它们的酸度在环己烯异构化和异丙苯裂解中进行了表征。催化剂的组成通过ICP测定。含有52重量%的亲本SA的渐进式浸出。%Al 2 O 3(SA52)导致Al 2 O 3含量的降低(33和19重量%,分别在MSA33和MSA19支持下)。这种减少伴随着BET表面积的增加和强酸的阐述。酸浸出呈正极地影响苯并噻吩HDS中硫化Como催化剂的活性,其略高于γ-Al2O3上负载的工业参考COMO催化剂的活性。

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