کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
58651 47161 2006 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
The structures of VOx/MOx and alkali-VOx/MOx catalysts and their catalytic performances for soot combustion
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
The structures of VOx/MOx and alkali-VOx/MOx catalysts and their catalytic performances for soot combustion
چکیده انگلیسی

Vanadium oxides supported on γ-Al2O3, SiO2, TiO2, and ZrO2 were studied on their molecular structures and reactive performances for soot combustion. To investigate the effect of different alkali metals on the structures and reactivities of supported-vanadium oxide catalysts, they were doped into the V4/TiO2 catalyst which had the best intrinsic activity for soot combustion in the selected supported vanadium oxide catalysts. The experimental results demonstrated that the catalytic properties of these catalysts depended on the vanadium loading amount, support nature, and the presence or the absence of alkali metals. The spectroscopic analysis (FT-IR and UV–vis) and H2-TPR results revealed that the higher activity of alkali-promoted vanadium oxide catalysts could be related to the ability of alkali metal promoting the redox cycle of the active vanadyl species. TG results showed that adding alkali to Vm/TiO2 catalyst was beneficial to lowering their melting points. Low melting points could ensure the good surface atom migration ability, which would improve the contact between the catalyst and soot. Due to the alkali metal components promoting the redox ability and the mobility of the catalysts, alkali-modified vanadium oxide catalysts could remarkably improve their catalytic activities for soot combustion. The catalytic activity order for soot combustion followed Li > Na > K > Rb > Cs in the catalyst system of alkali-V4/TiO2, and the reason why it followed this sequence was discussed.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Catalysis Today - Volume 118, Issues 3–4, 15 December 2006, Pages 315–322
نویسندگان
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