首页> 外文会议>The Belton Memorial Symposium Proceedings, Jan 10-11, 2000, Sydney, Australia >Rate of Interfacial Reaction Between Liquid Iron Oxide and CO-CO_2
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Rate of Interfacial Reaction Between Liquid Iron Oxide and CO-CO_2

机译:液态氧化铁与CO-CO_2之间的界面反应速率

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(1) Highly accurate, direct measurements of the gas (CO-CO_2) - slag (containing Fe_xO) reaction rate were accomplished by using a gravimetric technique. The rates measured in this study were controlled by the gas-slag interfacial reaction. (2) The apparent rate constants of the interfacial reactions between liquid iron oxide and CO and CO_2 gases at 1773 K, were given by k_(red) = 4.08 x 10~(-5) (P_(CO_2)/P_(CO))~(0.18) mol-O cm~(-2) s~(-1) atm~(-1) for the reduction and, k_(oxi.) = 3.86 x 10~(-5) (P_(CO_2)/P_(CO))~(-0.80) mol-O cm~(-2) s~(-1) atm~(-1) for the oxidation. (3) The apparent rate constant for liquid iron oxide, in equilibrium with solid iron at 1673 K, was 1.8 x10~(-5) mol-O.cm~(-2).s~(-1).atm~(-1), slightly higher than 1.13x10~(-5) mol-O cm~(-2) s~(-1) atm~(-1) obtained by Nagasaki from similar experiments. At 1673 K, the reduction rate constants for liquid iron oxide showed the same dependence on the slag oxidation state as that at 1773 K. They were given by k_(red) = 2.29x10~(-5)(P_(CO_2)/P_(CO))~(0.18) mol-O cm~(-2) s~(-1) atm~(-1) (4) Results similar to those on liquid iron oxide were obtained for the reduction and oxidation of alumina-saturated iron aluminate by CO and CO_2 gases, with an 18% decrease in the apparent rate constant at 1773 K. (5) The results for binary slag systems containing iron oxide indicate that the addition of basic oxides to iron oxide significantly increased the rate, whereas the addition of acidic oxides decreased the rate. (6) The 'charge transfer' mechanism was proposed to be the dominating mechanism of the reaction with minor effect from the 'site blockage'.
机译:(1)使用重量分析技术完成了对气体(CO-CO_2)-炉渣(含Fe_xO)反应速率的高精度直接测量。在这项研究中测得的速率是由气渣界面反应控制的。 (2)液态氧化铁与CO和CO_2气体在1773 K处的界面反应的表观速率常数由k_(red)= 4.08 x 10〜(-5)(P_(CO_2)/ P_(CO) )〜(0.18)mol-O cm〜(-2)s〜(-1)atm〜(-1)进行还原,k_(oxi。)= 3.86 x 10〜(-5)(P_(CO_2) /P_(CO))~(-0.80)mol-O cm〜(-2)s〜(-1)atm〜(-1)进行氧化。 (3)液态铁氧化物在1673 K下与固态铁平衡时的表观速率常数为1.8 x10〜(-5)mol-O.cm〜(-2).s〜(-1).atm〜( -1),稍高于长崎从类似实验获得的1.13x10〜(-5)mol-O cm〜(-2)s〜(-1)atm〜(-1)。在1673 K时,液态氧化铁的还原速率常数与1773 K时对渣氧化态的依赖性相同。它们由k_(red)= 2.29x10〜(-5)(P_(CO_2)/ P_ (CO))〜(0.18)mol-O cm〜(-2)s〜(-1)atm〜(-1)(4)获得了与液态氧化铁类似的还原和氧化氧化铝的结果。由CO和CO_2气体产生的饱和铝酸铁,其表观速率常数在1773 K处降低了18%。(5)含氧化铁的二元炉渣系统的结果表明,向氧化铁中添加碱性氧化物会显着提高速率,而添加酸性氧化物会降低该速率。 (6)提出“电荷转移”机制是反应的主要机制,受“位阻”影响较小。

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