کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
43762 45987 2008 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Performance of Pt-Fe/mordenite monolithic catalysts for preferential oxidation of carbon monoxide in a reformate gas for PEFCs
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
Performance of Pt-Fe/mordenite monolithic catalysts for preferential oxidation of carbon monoxide in a reformate gas for PEFCs
چکیده انگلیسی

Pt-Fe/mordenite catalysts coated on ceramic straight-channel monoliths were evaluated for the preferential oxidation of carbon monoxide (PROX) in hydrogen-rich gas streams. In a feed gas containing 1% CO, 1% O2, with the balance H2, CO conversion reached almost 100% at temperatures ranging from 100 to 130 °C, i.e., an outlet CO concentration of less than 10 ppm. Even in a synthetic reformate gas (1% CO, 1% O2, 15% H2O, 20% CO2, balance H2), the monolithic catalyst exhibited excellent activity, reducing the CO concentration to less than 100 ppm. In particular, under optimized conditions, an outlet CO concentration of less than 10 ppm was realized. This is the first report that has demonstrated that monolithic catalysts could achieve the 10-ppm target level at a low O2/CO ratio and a high space velocity in a single-stage reactor. Excellent durability of the monolithic catalyst is expected, based on a lack of deterioration in performance during 500 h of operation.

Pt-Fe/mordenite catalysts coated on ceramic monoliths were evaluated for the preferential oxidation of carbon monoxide (PROX) in hydrogen-rich gas stream. The monolithic catalyst exhibited an excellent activity, reducing CO concentration to less than 10 ppm under optimized conditions. This is the first report that has demonstrated that monolithic catalysts could achieve the 10 ppm target level at a low O2/CO ratio and a high space velocity.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Applied Catalysis A: General - Volume 341, Issues 1–2, 15 June 2008, Pages 93–97
نویسندگان
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