کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
233355 465336 2013 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
TGA kinetic study on the hydrogen reduction of an iron nickel oxide
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی مهندسی شیمی (عمومی)
پیش نمایش صفحه اول مقاله
TGA kinetic study on the hydrogen reduction of an iron nickel oxide
چکیده انگلیسی


• We examine the kinetics for the hydrogen reduction of an iron nickel oxide.
• Chemical reactions control the reduction rate below 600 °C.
• Gas diffusion through the sample control the reduction rate between 600 and 1200 °C.
• Decrease in sample porosity reduces the reduction rate above 1200 °C.
• Reduction rate increases with the increase of PH2 with the reaction order of 1.44.

Reduction of a mixed iron nickel oxide by hydrogen to produce ferronickel alloy was investigated by thermo-gravimetric analysis (TGA). The iron nickel oxide, which contains 50 wt% Fe and 10 wt% Ni mainly in the form of hematite (Fe2O3) and nickel ferrite (NiFe2O4), is a residue produced from the water leaching of a selectively sulfation roasted nickel calcine. Continuous heating tests with a fixed heating rate as well as isothermal tests were performed. Results indicate that the reduction of the mixed oxide began above 350 °C. The reduction reactions occurred in a non-topochemical mode at low temperatures between 350 °C and 600 °C with its rate controlled by the solid–gas chemical reactions. The reduction rate increased with the increase in temperature from 350 °C up to 1100 °C. Between 600 °C and 1200 °C, the rate controlling step was the diffusion of reducing gas through the pores of the sample bed with an apparent activation energy of 34.1 kJ/mol. Due to the melting of the silicate material at 1200 °C which substantially reduced the sample porosity, the reduction rate decreased. Above 1200 °C, the reduction rate increased again due to the increased diffusion of the reducing gas through the molten sample at higher temperatures.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Minerals Engineering - Volume 54, December 2013, Pages 32–38
نویسندگان
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