کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
58426 47151 2006 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
HDS and deep HDS activity of CoMoS-mesostructured clay catalysts
کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
HDS and deep HDS activity of CoMoS-mesostructured clay catalysts
چکیده انگلیسی

The goal of this work is to identify more promising supports from synthetic clay materials to advance hydrotreating catalyst development. Silica sol can be used as the silicon-containing starting material when creating nanoporous layered silicate catalysts with a certain portion of unreacted sol particles incorporated into the final matrix. The resulting structure then has mesoporosity and a unique morphology. Hectorite-based clays have been prepared using different silica sols in order to ascertain the importance of sol characteristics on the final matrix. Several techniques have been applied to characterize the materials, including XRD, TGA, N2 porosimetry, and TEM. For hydrodesulfurization (HDS), the conversion of dibenzothiophene (DBT) to biphenyl was examined at 400 °C using CoMoS-loaded mesostructured clay supports. No hydrogenation or hydrocracking was observed with any of the clay supports. The most active clay was derived from Ludox silica sol AS-30 with an activity of 65% DBT conversion and 100% selectivity to biphenyl (BP). For comparison, a reference commercial catalyst displayed 94% BP selectivity. For deep HDS, the conversion of 4,6-dimethyldibenzothiophene was tested at 325 and 350 °C. At 325 °C, conversions are 92% of commercial catalysts for a CoMoS-loaded mesostructured clay derived from Ludox AM-30 silica sol. A commercially available synthetic hectorite called laponite has very low activity, indicating that the unique morphology of the mesostructured clays is important. Hydrogenolysis vs. hydrogenation pathways are compared for the deep HDS reaction. HR-TEM of the most active deep HDS catalyst revealed a multilayered MoS2 morphology.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Catalysis Today - Volume 116, Issue 4, 15 September 2006, Pages 478–484
نویسندگان
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