Peng Hao, Guo Jing, Huang Huisheng, Li Bing, Zhang Xingran
Chongqing Key Laboratory of Inorganic Special Functional Materials, College of Chemistry and Chemical Engineering, Yangtze Normal University, Fuling, Chongqing 408100, P. R. China.
College of Chemistry and Chemical Engineering, Chongqing University of Technology, Chongqing 400054, P. R. China.
ACS Omega. 2021 Oct 7;6(41):27478-27484. doi: 10.1021/acsomega.1c04397. eCollection 2021 Oct 19.
This paper focused on the oxidation-alkaline extraction process of vanadium-chromium-reducing residue. The affected parameters including reaction temperature, KMnO dosage, reaction time, NaOH dosage, and liquid-to-solid ratio on the extraction process were investigated. The E-pH diagram and the thermodynamic analysis indicated that KMnO was suitable for the oxidation of low-valence vanadium and chromium. Vanadium (97.24%) and chromium (56.20%) were extracted under the following optimal reaction conditions: reaction temperature of 90 °C, reaction time of 90 min, dosage of KMnO at (KMnO)/(residue) = 0.40, dosage of NaOH at (NaOH)/(residue) = 0.30, and liquid-to-solid ratio at 5:1 mL/g. The extraction process of vanadium was controlled by the reactant through the solid product layer and the extraction kinetics behavior fitted well with the shrink core model with an of 15.37 kJ/mol. At the same time, the surface chemical reaction was the controlling step for chromium extraction, which was difficult with an of 39.78 kJ/mol.
本文重点研究了钒铬还原渣的氧化-碱浸出工艺。考察了反应温度、高锰酸钾用量、反应时间、氢氧化钠用量和液固比对浸出过程的影响参数。E-pH图和热力学分析表明,高锰酸钾适合于低价钒和铬的氧化。在以下最佳反应条件下,钒(97.24%)和铬(56.20%)被浸出:反应温度90℃,反应时间90分钟,高锰酸钾用量为(高锰酸钾)/(渣)=0.40,氢氧化钠用量为(氢氧化钠)/(渣)=0.30,液固比为5:1 mL/g。钒的浸出过程受反应物通过固体产物层的控制,浸出动力学行为与收缩核模型拟合良好,活化能为15.37 kJ/mol。同时,表面化学反应是铬浸出的控制步骤,该过程较难进行,活化能为39.78 kJ/mol。