کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
41465 45890 2011 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Avoiding the deactivation of sulphated MoOx/TiO2 catalysts in the photocatalytic cyclohexane oxidative dehydrogenation by a fluidized bed photoreactor
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
Avoiding the deactivation of sulphated MoOx/TiO2 catalysts in the photocatalytic cyclohexane oxidative dehydrogenation by a fluidized bed photoreactor
چکیده انگلیسی

Since the relevance of deactivation phenomena in heterogeneous gas–solid photocatalytic processes, a study on the deactivation of MoOx/TiO2 catalysts in the oxidative photodehydrogenation of cyclohexane has been carried out in a fixed bed reactor and compared to the behaviour of catalysts used in a two-dimensional fluidized bed photoreactor.Superior photocatalytic performances were obtained in the fluidized bed reactor with respect to the fixed bed reactor both in terms of cyclohexane conversion and benzene yield. At the opposite of the fixed bed, in the fluidized bed reactor, catalyst did not deactivate. Characterization performed on catalysts after photocatalytic tests evidenced that the deactivation of the catalysts is correlated to the accumulation of carbonaceous species on catalyst surface and the sulphur disappearance. The catalysts used in fluidized conditions remained active as they maintained their initial sulphur content at the surface.

Figure optionsDownload high-quality image (152 K)Download as PowerPoint slideResearch highlights▶ Higher photoactivity in the fluidized bed reactor with respect to fixed bed. ▶ Activity improvement in fluidized bed due to the minimization of light scattering. ▶ No catalyst deactivation in the fluidized bed reactor. ▶ Presence of catalyst deactivation in the fixed bed reactor. ▶ Catalyst deactivation by accumulation of carbon species and sulphur disappearance.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Applied Catalysis A: General - Volume 394, Issues 1–2, 28 February 2011, Pages 71–78
نویسندگان
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