Alastraet： The gas-based direct reduction of iron ore pellets was carried out by simulating the typical gas composition in coal gasification process, Midrex and HyMII processes. The influences of gas composition and ...Alastraet： The gas-based direct reduction of iron ore pellets was carried out by simulating the typical gas composition in coal gasification process, Midrex and HyMII processes. The influences of gas composition and temperature on reduction were studied. Results show that the increasing of HE proportion is helpful to improve the reduction rate. However, when ~o（H2）：~o（CO）〉1.6：1, changes of HE content have little influence on it. Appropriate reduction temperature is about 950 ℃, and higher temperature （1 000 ℃） may unfavorably slow the reduction rate. From the kinetics analysis at 950 ℃, the most part of reduction course is likely controlled by interfacial chemical reaction mechanism and in the final stage controlled by a combined effect of gaseous diffusion and interfacial chemical reaction mechanisms. From the utilizations study of different reducing gases at 950 ℃, the key step in reduction course is the 3rd stage （FeO→Fe）, and the utilization of reducing gas increases with the rise of HE proportion.展开更多
In gaseous reduction of iron ore fines, alkaline earth oxides have profound effects on the precipitation behavior of fresh metal- lic iron on the particle surface. In this work, in situ observation was performed to re...In gaseous reduction of iron ore fines, alkaline earth oxides have profound effects on the precipitation behavior of fresh metal- lic iron on the particle surface. In this work, in situ observation was performed to reveal the influence of alkaline earth oxides on the precipitation morphology and micro-structure variation of fresh metallic iron from microscopic level by simulation of the gas-solid reaction condition on the surface of ore particles. Experimental results indicate that doping MgO in the particle surface can inhibit the reduction of iron oxide and however doping CaO, SrO and BaO promote; all alkaline earth oxides tested in this study can change the precipitation morphology of fresh metallic iron; minimum doping mole fraction of one oxide to inhibit iron whiskers growth （ NAO ） is related to its cation radius （ r：＋ ） and its extranuclear electronic layers（nAD ）, which can be expressed as NAO = 1.3 × 10^-5r^2AD,√nA^2.展开更多
Oxide nanostructures grown on noble metal surfaces are often highly active in many reactions,in which the oxide/metal interfaces play an important role.In the present work,we studied the surface structures of Fe Ox-on...Oxide nanostructures grown on noble metal surfaces are often highly active in many reactions,in which the oxide/metal interfaces play an important role.In the present work,we studied the surface structures of Fe Ox-on-Pt and Ni Ox-on-Pt catalysts and their activity to CO oxidation reactions using both model catalysts and supported nanocatalysts.Although the active Fe O1x structure is stabilized on the Pt surface in a reductive reaction atmosphere,it is prone to change to an Fe O2x structure in oxidative reaction gases and becomes deactivated.In contrast,a Ni O1x surface structure supported on Pt is stable in both reductive and oxidative CO oxidation atmospheres.Consequently,CO oxidation over the Ni O1x-on-Pt catalyst is further enhanced in the CO oxidation atmosphere with an excess of O2.The present results demonstrate that the stability of the active oxide surface phases depends on the stabilization effect of the substrate surface and is also related to whether the oxide exhibits a variable oxidation state.展开更多
基金Project(50725416) supported by National Natural Science Funds for Distinguished Young Scholars of China
文摘Alastraet： The gas-based direct reduction of iron ore pellets was carried out by simulating the typical gas composition in coal gasification process, Midrex and HyMII processes. The influences of gas composition and temperature on reduction were studied. Results show that the increasing of HE proportion is helpful to improve the reduction rate. However, when ~o（H2）：~o（CO）〉1.6：1, changes of HE content have little influence on it. Appropriate reduction temperature is about 950 ℃, and higher temperature （1 000 ℃） may unfavorably slow the reduction rate. From the kinetics analysis at 950 ℃, the most part of reduction course is likely controlled by interfacial chemical reaction mechanism and in the final stage controlled by a combined effect of gaseous diffusion and interfacial chemical reaction mechanisms. From the utilizations study of different reducing gases at 950 ℃, the key step in reduction course is the 3rd stage （FeO→Fe）, and the utilization of reducing gas increases with the rise of HE proportion.
基金supported by the National Natural Science Foundation of China and Baosteel (Grant No.50834007)the National Basic Research Program of China (973 Program) (Grant No.2012CB720401)
文摘In gaseous reduction of iron ore fines, alkaline earth oxides have profound effects on the precipitation behavior of fresh metal- lic iron on the particle surface. In this work, in situ observation was performed to reveal the influence of alkaline earth oxides on the precipitation morphology and micro-structure variation of fresh metallic iron from microscopic level by simulation of the gas-solid reaction condition on the surface of ore particles. Experimental results indicate that doping MgO in the particle surface can inhibit the reduction of iron oxide and however doping CaO, SrO and BaO promote; all alkaline earth oxides tested in this study can change the precipitation morphology of fresh metallic iron; minimum doping mole fraction of one oxide to inhibit iron whiskers growth （ NAO ） is related to its cation radius （ r：＋ ） and its extranuclear electronic layers（nAD ）, which can be expressed as NAO = 1.3 × 10^-5r^2AD,√nA^2.
基金financially supported by the National Natural Science Foundation of China(21222305,11079005,20923001)the National Basic Research Program of China(2011CBA00503,2013CB933100)
文摘Oxide nanostructures grown on noble metal surfaces are often highly active in many reactions,in which the oxide/metal interfaces play an important role.In the present work,we studied the surface structures of Fe Ox-on-Pt and Ni Ox-on-Pt catalysts and their activity to CO oxidation reactions using both model catalysts and supported nanocatalysts.Although the active Fe O1x structure is stabilized on the Pt surface in a reductive reaction atmosphere,it is prone to change to an Fe O2x structure in oxidative reaction gases and becomes deactivated.In contrast,a Ni O1x surface structure supported on Pt is stable in both reductive and oxidative CO oxidation atmospheres.Consequently,CO oxidation over the Ni O1x-on-Pt catalyst is further enhanced in the CO oxidation atmosphere with an excess of O2.The present results demonstrate that the stability of the active oxide surface phases depends on the stabilization effect of the substrate surface and is also related to whether the oxide exhibits a variable oxidation state.
