کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | ترجمه فارسی | نسخه تمام متن |
---|---|---|---|---|---|
6630502 | 1424932 | 2018 | 9 صفحه PDF | سفارش دهید | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Catalytic activity of electrodeposited cobalt oxide films for methane combustion in a micro-channel reactor
ترجمه فارسی عنوان
فعالیت کاتالیستی فیلم های اکسید کبالت الکترودهایی برای احتراق متان در یک راکتور میکرو کانال
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی شیمی
مهندسی شیمی (عمومی)
چکیده انگلیسی
This paper studies the catalytic combustion of a methane-air mixture inside a micro-channel reactor coated with cobalt oxide (Co3O4) film. The Co3O4 was coated on the reactor channels by an inexpensive electrodeposition method. A cohesive film with large accessible surface area was fabricated with the method described, which allowed the control of the film thickness. Complete combustion of methane was achieved at 760â¯Â°C. The catalytic activity profiles obtained suggest that the reaction is carried only via catalytic combustion up to 600â¯Â°C, while both gas-phase and catalytic combustion might occur simultaneously at higher temperatures. The measured catalytic reaction rate per unit area was aligned with the reaction rate reported for similar reactors and operating conditions. Results showed that the catalytic films did not deactivate after a total of 50â¯h of cyclic operation. Tests with different reactants concentration revealed a first order dependence of the reaction rates for methane concentration and a near zero-order dependence on the oxygen concentration, at 600â¯Â°C. The measured data was successfully fitted by a chemistry model proposed in the literature. Overall, this work highlights the potential of using inexpensive electrodeposited films of Co3O4 on micro-channel reactors for combustion of hydrocarbons.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Fuel - Volume 232, 15 November 2018, Pages 51-59
Journal: Fuel - Volume 232, 15 November 2018, Pages 51-59
نویسندگان
José M. Rodrigues, M. Filipa Ribeiro, Edgar C. Fernandes,
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