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Effect of CaCl2 Addition on Phosphorus Distribution Between CaO–SiO2–FeOx–P2O5 Slag and Carbon-Saturated Iron at Steelmaking Temperature
Metallurgical and Materials Transactions B ( IF 3 ) Pub Date : 2021-06-11 , DOI: 10.1007/s11663-021-02236-0
Ziwen Yan , Zhiyin Deng , Miaoyong Zhu

To understand the effect of CaCl2 addition on the dephosphorization ability of steelmaking slags, laboratory experiments were carried out to study the phosphorus distribution between CaO–SiO2–FeOx–P2O5–CaCl2 slags and carbon-saturated iron at steelmaking temperature. The phosphorus distribution ratio between slag and pure iron foil (\( L_{\text{P}}^{{{\text{Fe-}}\gamma }} \)) was measured by equilibrium experiments and converted into the phosphorus distribution ratio between slag and carbon-saturated iron (\( L_{\text{P}}^{{\text{Fe}}{-}{\text{C}}} \)) using thermodynamic calculations. The influential mechanism of CaCl2 was also discussed based on the phases in the slags. It was found that the addition of CaCl2 is beneficial for the improvement of \( L_{\text{P}}^{{{\text{Fe}}{-}{\text{C}}}} \). In the slag with basicity (R = [w(CaO)/w(SiO2)]) of 1.0, the P content in the liquid slag was increased by the addition of CaCl2. When the basicity is sufficiently high (e.g., R≥1.5), the addition of CaCl2 enhances the generation of P-rich solid phases, including both 2CaO·SiO2–3CaO·P2O5 (C2S–C3P) and Ca5Cl(PO4)3. Compared with CaCl2-free slags, CaCl2 addition in BOF slags doesn’t evidently change the effects of slag basicity and FeOx content. With the increase of slag basicity (1.0 to 2.0), the amount of C2S–C3P solid solution in the slag climbs obviously, resulting in a higher \( L_{\text{P}}^{{{\text{Fe}}{-}{\text{C}}}} \) both in CaCl2-added slags and CaCl2-free slags, while \( L_{\text{P}}^{{{\text{Fe}}{-}{\text{C}}}} \) increases first and then decreases when the FeOx content varies from 15 to 35 pct in this study.



中文翻译:

CaCl2添加对炼钢温度下CaO-SiO2-FeOx-P2O5渣与碳饱和铁之间磷分布的影响

为了解CaCl 2添加对炼钢渣脱磷能力的影响,通过室内实验研究了CaO-SiO 2 -FeO x -P 2 O 5 -CaCl 2渣与碳饱和铁在炼钢过程中的磷分布温度。炉渣与纯铁箔之间的磷分布比(\( L_{\text{P}}^{{{\text{Fe-}}\gamma }} \))通过平衡实验测量并转化为磷分布炉渣和碳饱和铁之间的比率(\( L_{\text{P}}^{{\text{Fe}}{-}{\text{C}}} \))使用热力学计算。CaCl的影响机制2还基于炉渣中的相进行了讨论。发现加入CaCl 2有利于\( L_{\text{P}}^{{{\text{Fe}}{-}{\text{C}}}} \)的提高。在碱度( R  = [ w (CaO)/ w (SiO 2 )]) 为1.0 的炉渣中,通过添加CaCl 2提高了液态炉渣中P 的含量。当碱度足够高(例如- [R ≥1.5),添加氯化钙的2增强P-富固体相的产生,包括2CaO·的SiO 2 -3CaO·P 2 ø 5(C 2S–C 3 P) 和 Ca 5 Cl(PO 4 ) 3。与不含CaCl 2 的炉渣相比,转炉炉渣中CaCl 2 的添加并未明显改变炉渣碱度和FeO x含量的影响。随着炉渣碱度的增加(1.0~2.0),炉渣中C 2 S-C 3 P固溶体量明显增加,导致\( L_{\text{P}}^{{{\text {Fe}}{-}{\text{C}}}} \)在添加 CaCl 2 的渣和不含 CaCl 2 的渣中,而\( L_{\text{P}}^{{{\text{ Fe}}{-}{\text{C}}}} \)先增加后减少,当 FeO x 在这项研究中,内容从 15 到 35 pct 不等。

更新日期:2021-06-13
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