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Hydrodesulfurization of 4,6-dimethyldibenzothiophene over Pt,Pd,and Pt-Pd catalysts supported on amorphous silica-alumina

机译:在无定形二氧化硅-氧化铝上负载的Pt,Pd和Pt-Pd催化剂上的4,6-二甲基二苯并噻吩加氢脱硫

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摘要

The activities and selectivities of Pt,Pd,and Pt-Pd supported on amorphous silica-alumina (ASA) in the hydrodesulfurization (HDS) of 4,6-dimethyldibenzothiophene (4,6-DM-DBT) were investigated.The ASA-supported catalysts had much higher activities than alumina-supported catalysts,due to the creation of electron-deficient metal particles.Pd had a high hydrogenation activity for 4,6-DM-DBT,but the removal of sulfur from 4,6-DM-DBT and its HDS intermediates occurred faster over Pt than over Pd.Comparison of two Pt/ASA catalysts with different Pt loadings showed that the metal dispersion strongly influenced the product selectivity.Larger metal particles led to relatively faster hydrogenation and slower C-S bond breaking.Bimetallic Pt-Pd catalysts were much more active than the monometallic constituents,indicating that the metal particles were alloyed.Acid-catalyzed cracking and isomerization occurred especially over Pt/ASA.
机译:研究了无定形二氧化硅-氧化铝(ASA)上Pt,Pd和Pt-Pd在4,6-二甲基二苯并噻吩(4,6-DM-DBT)的加氢脱硫(HDS)中的活性和选择性。 Pd对4,6-DM-DBT具有较高的加氢活性,但从4,6-DM-DBT中去除了硫,因此其活性比氧化铝负载的催化剂高得多。两种Pt / ASA催化剂负载不同的Pt / ASA催化剂的比较表明,金属分散度强烈影响产物的选择性,较大的金属颗粒导致相对较快的加氢和较慢的CS键断裂。 -Pd催化剂比单金属成分具有更高的活性,表明金属颗粒是合金化的。尤其在Pt / ASA上发生了酸催化的裂解和异构化。

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