首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >Hydrodesulfurization of sulfur-containing polyaromatic compounds in light gas oil using noble metal catalysts
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Hydrodesulfurization of sulfur-containing polyaromatic compounds in light gas oil using noble metal catalysts

机译:贵金属催化剂在轻质轻质油中对含硫多芳族化合物进行加氢脱硫

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摘要

We systematically monitored the hydrodesulfurization (HDS) activity of dibenzothiophene (DBT) and groups of substituted DBTs present in a SR-LGO over various noble metal catalysts (Ru,Rh,Ru-Rh,Pt,Pd and Pt-Pd) supported on alumina.The catalytic performances were compared to those obtained over a conventional CoMo catalyst.The Pd-based catalysts exhibited excellent HDS performances,especially for desulfurizing the refractory compounds.In particular,the 4,6-dimethyldibenzothiophene (4,6-DMDBT) HDS activity over the Pd or the Pd-Pt catalyst was equivalent to that over the CoMo catalyst.This was attributed to the exceptional hydrogenation (HYD) properties of the Pd-based catalysts,which enable desulfuri/ation of the refractory compounds by considerably minimizing the effect of the steric hindrance due to their substituents.The synergetic effect observed on the bimetallic Pt-Pd system at low temperature for all the sulfur compounds was largely attenuated in the high temperature range,probably due to shifting of the HYD/dehydrogenation equilibrium to dehydrogenation.Despite a much lower metal loading (0.25 wt.%),the performances of the Rh catalyst were superior to those of the optimized 16 wt.% Ru catalyst.A synergetic effect was observed on the Ru-Rh catalyst,on which the DBT HDS activity was significantly enhanced compared to the activity of each corresponding monometallic catalyst.Further,we recently showed that the use of SiO_2 or SiO_2-Al_2O_3 as a support allows higher optimal Rh contents,making the Rh-based HDS catalysts even more promising.In brief,we obtained encouraging results,which showed for instance that the excellent properties of the noble metal catalysts in model HDS reactions are still observed during the HDS treatment of real feeds.
机译:我们系统地监测了负载在氧化铝上的各种贵金属催化剂(Ru,Rh,Ru-Rh,Pt,Pd和Pt-Pd)上二苯并噻吩(DBT)的加氢脱硫(HDS)活性和SR-LGO中存在的取代DBT的基团与传统CoMo催化剂获得的催化性能进行了比较.Pd基催化剂表现出出色的HDS性能,特别是用于难熔化合物的脱硫,特别是4,6-二甲基二苯并噻吩(4,6-DMDBT)HDS活性在Pd或Pd-Pt催化剂上的催化性能与在CoMo催化剂上的催化性能相同,这归因于Pd基催化剂的出色的氢化(HYD)性能,可通过最大程度地减少影响来实现耐火化合物的脱硫/加氢在低温下对双金属Pt-Pd系统观察到的所有硫化合物的协同作用在高温范围内大大减弱,probab尽管金属负载量(0.25 wt。%)低得多,但Rh催化剂的性能优于优化的16 wt。%Ru催化剂。协同作用是在Ru-Rh催化剂上观察到,与每种相应的单金属催化剂的活性相比,DBT HDS活性显着增强。此外,我们最近表明,使用SiO_2或SiO_2-Al_2O_3作为载体可以得到更高的最佳Rh含量,简而言之,我们获得了令人鼓舞的结果,例如表明,在真实进料的HDS处理过程中,仍观察到贵金属催化剂在模型HDS反应中的优异性能。

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