کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
67232 48472 2009 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Production of hydrogen by partial oxidation of methanol over bimetallic Au–Cu/TiO2–Fe2O3 catalysts
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
Production of hydrogen by partial oxidation of methanol over bimetallic Au–Cu/TiO2–Fe2O3 catalysts
چکیده انگلیسی

Partial oxidation of methanol (POM) to produce H2 was investigated over Au–Cu/TiO2 and Au–Cu/TiO2–Fe2O3 catalysts. The catalysts were prepared by deposition-precipitation method and characterized by XRD, TEM, HRTEM, ICP-AES, TPR, NH3-TPD and XPS analyses. Detail study on the Au–Cu/TiO2–Fe2O3 catalysts was performed to optimize Ti/Fe ratio, pH during preparation of the catalyst, calcination temperature and reaction temperature. The Au–Cu/TiO2–Fe2O3 catalyst with Ti/Fe = 9/1 atomic ratio is more active and exhibits higher methanol conversion compared to the Au–Cu/TiO2 catalyst. The higher activity of Fe-containing catalyst was attributed to the ability to supply reactive oxygen, thereby stabilize active gold species (Auδ+) in the catalyst. Studies on the optimization of pH during preparation of the Au–Cu/TiO2–Fe2O3 catalyst and calcination temperature showed that the catalyst prepared at pH 7 and dried at 373 K (uncalcined) exhibited higher activity. The catalytic performance at various reaction temperatures shows that both methanol conversion and hydrogen selectivity are increased with increasing the temperature. A small increase in CO selectivity was observed beyond 523 K, which is due to the decomposition of methanol and reverse water gas shift at high temperatures.

Partial oxidation of methanol to produce H2 was investigated over Au–Cu/TiO2 and Au–Cu/TiO2–Fe2O3 catalysts. The Au–Cu/TiO2–Fe2O3 catalyst with Ti/Fe = 9/1 atomic ratio is more active compared to the Au–Cu/TiO2 catalyst. The higher activity of Fe-containing catalyst was attributed to the stabilization of active gold species (Auδ+) in the catalyst.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Molecular Catalysis A: Chemical - Volume 313, Issues 1–2, 2 November 2009, Pages 55–64
نویسندگان
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