共查询到18条相似文献,搜索用时 93 毫秒
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如何降低不锈钢中的磷改善其质量是冶金工作者一直关心的问题,本文综述了近十多年来对不锈钢氧化脱磷的研究成果,表明BaO渣系是不锈钢脱磷的最有效渣系之一,CaO渣系由于其价格便宜,资源丰富,可作为不锈钢锐磷的最一般渣系,利用氧化钡和氧化钙混合渣系有很好的发展前景,碱金属氧化物渣系对不锈钢的脱磷还有待于进一步研究。 相似文献
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利用耦合反应动力学模型模拟了不锈钢的氧化脱磷过程,与试验结果的对比表明该模型对描述不锈钢脱磷过程是适用的。 相似文献
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不锈钢弱氧化脱磷实验研究 总被引:5,自引:0,他引:5
研究了CaO—BaO—CaF_2熔剂的配比和氧化剂添加量等对18—8([%C]_0=0.30~0.35)熔体脱磷的影响以及熔剂中配入适量Cr_2O_3的作用。实验结果表明,当熔剂量为70kg/t时可获得39%~53%的脱磷率,并有较好的保铬作用。还分析了不锈钢弱氧化脱磷的热力学条件。 相似文献
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不锈钢弱氧化脱磷工业试验研究 总被引:1,自引:0,他引:1
介绍在电弧炉中应用CaO-BaCO3-CaF2熔剂在18-8不锈钢初炼钢液(%C)=1.34(%Cr)=18.02)进行脱磷试验情况,试验结果表明,当熔剂量在60kg/t钢时,可获得33%的脱磷率,并有较好的保铬作用,分析了不锈钢弱氧化脱磷的热力学条件及工艺因素。 相似文献
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JIANG Guo-chang GUO Shu-qiang ZHANG Xiao-bing ZHUANG Yun-qian XU Kuang-di 《钢铁研究学报(英文版)》2000,7(2):50-54
In the scale of ironmaking and steelmaking, the dephosphorization can be divided into four classes. The first level which is known very well by metallurgists is the dephosphorization for carbon steels and low alloy steels. The second level is that included in the pretreatment process of hot metal. It differs from the first level as it must consider how to treat the selective oxidation of [P] and [C]. Furthermore, The contradictory of dephosphorization and desulphurization has to be harmonized. The third level is that for high alloy steels and the fourth is that for ferroalloys. In these cases, two technical ways either oxidizing dephosphorization or reducing dephosphorization can be selected. Whether which one is chosen, the key problem is to lower down phosphorous content efficiently meanwhile to keep the concentration of Cr and/or Mn almost lossless.
The cheapest raw materials for the production of high alloy steel are the returning scrap of that steel. Raising the proportion of the returning scraps in the total amount of raw materials is a very important measure to decrease the production cost. In order to avoid an obvious oxidation of Cr, Mn and so on during that melting process it is impossible to adopt the oxidational dephosphorization procedures which is generally carried out in the production of low alloy steel. In this case, after returning several times the phosphorous content in the scraps is accumulated. And then it gradually approaches to the level specified in the standard of the steel. Finally, it will become a waste. It was estimated that the market demand on high alloy steels as stainless steels would rapidly grow. So the scraps containing low phosphorous is urgently needed in a great deal.
On the other hand, the standards of some high alloy steels, which are designated for extremely severe environment only, allow a very low phosphorous content. For example, it is claimed that W[P]<0.015 %—0.020 % if the stainless steel products will contact with urea or nitric acid. If the resistance to corrosive fatigue and welding crack is highlighted the phosphorous content should be decreased to less than (100—50)×10-4 %. And Koros P J et al estimated that dephosphorous to 14×10-4 % will be wanted[1].
So far no technology for dephosphorization of stainless steels can be widely adopted in industrial scale. This will be one of the major research projects in the coming century. This paper devotes to a discussion on the strategy of oxidational dephosphorization and the improvement of the reductional dephosphorization. 相似文献
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Sander Arnout Frederik Verhaeghe Bart Blanpain Patrick Wollants Roel Hendrickx Gert Heylen 《国际钢铁研究》2006,77(5):317-323
A time‐dependent thermochemical model has been developed for the electric arc furnace (EAF) process for stainless steel production. Time dependency is implemented by a stepwise input of energy and matter into an equilibrium reactor. The equilibrium calculations are performed using data from FACT‐databases and implemented using the programming library ChemApp. The material input for the model was generated by reconciliation of industrial data and the energy input is approximated from the industrial data and scaled through an efficiency factor. The model is used to calculate the evolution of temperature and composition of gas, slag and metal phases with time. Agreement of the end composition in the metal phase with industrial data is good. In the slag phase, however, Cr, Fe, Mn and Si are oxidized significantly less than expected due to excess formation of CO‐gas. The dynamics of the slag composition are examined in more detail. Here a fair agreement is reached for the main slag components. However, for Cr, Fe and Mn the model cannot predict the dynamics, which seem to be strongly kinetically controlled. The results of the equilibrium model can thus provide some insight into the kinetics of the process. 相似文献
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在MoSi2炉和MgO坩埚内进行了含钡合金处理316L不锈钢液的实验研究.实验选用的含钡合金为SiCaBa、SiAlBaCa和SiCaBaMg,并与SiCa和AlCa合金的处理结果进行了对比.实验中发现,使用含钡合金处理钢液时,钡在处理初期就参与了脱氧反应,生成含钡的复合氧-硫化物夹杂,更易于上浮排除,全氧含量能够快速降低至较低的水平;在钙合金中添加钡、镁等元素后,合金的脱硫能力提高;SiCaBa合金的还原脱磷效果最佳,用SiAlBaCa合金处理钢液时未出现回磷现象. 相似文献
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