کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
675616 | 1459609 | 2008 | 7 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
A study on the kinetics of hydrogen reduction of molybdenum disulphide powders
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی شیمی
جریان سیال و فرایندهای انتقال
پیش نمایش صفحه اول مقاله
![عکس صفحه اول مقاله: A study on the kinetics of hydrogen reduction of molybdenum disulphide powders A study on the kinetics of hydrogen reduction of molybdenum disulphide powders](/preview/png/675616.png)
چکیده انگلیسی
In order to achieve direct reduction of molybdenite in presence of a sulphur scavenger such as CaO such that SO2 emission is completely avoided, it is important to maximise the rate of the partial reaction involving molybdenite and hydrogen (without lime) given the low thermodynamic driving force for this reaction. Accordingly, reaction of molybdenum disulphide powders with hydrogen was investigated by thermogravimetric method. Effect of temperature and concentration on the reaction rate was studied under such conditions that resistance to mass transfer arising from external film, between particles and intra-grain was negligible. The operating temperature ranged between 973 and 1173 K while the hydrogen concentration was varied between 30 and 100%. The experimental data obtained under the above conditions were analyzed by applying “the shrinking unreacted core model”. The reduction reaction was found to be first order with respect to the gaseous reactant. Pre-exponential factor and activation energy have been determined to be 3.91 Ã 103 cm minâ1 and 139.0 kJ molâ1, respectively. Activation energy obtained from a fitted model, agreed well with the values determined from the model-free methods using isothermal measurements.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Thermochimica Acta - Volume 473, Issues 1â2, 10 July 2008, Pages 61-67
Journal: Thermochimica Acta - Volume 473, Issues 1â2, 10 July 2008, Pages 61-67
نویسندگان
M. Mehdi Afsahi, Morteza Sohrabi, R. Vasant Kumar, Habib Ale Ebrahim,