中国有色金属学报
中國有色金屬學報
중국유색금속학보
THE CHINESE JOURNAL OF NONFERROUS METALS
2014年
8期
2137-2144
,共8页
张晓伟%李梅%柳召刚%胡艳宏%王觅堂%刘佳%阳建平
張曉偉%李梅%柳召剛%鬍豔宏%王覓堂%劉佳%暘建平
장효위%리매%류소강%호염굉%왕멱당%류가%양건평
氯化铝%盐酸%浸出%稀土精矿%动力学%活化能
氯化鋁%鹽痠%浸齣%稀土精礦%動力學%活化能
록화려%염산%침출%희토정광%동역학%활화능
aluminium chloride%hydrochloric acid%leaching%mixed rare earth concentrate%kinetics%activation energy
采用氯化铝盐酸体系配合浸出包头混合稀土精矿,并对浸出过程动力学进行研究,浸出过程主要考察盐酸和氯化铝的浓度、液固比、搅拌速度、温度及反应时间对精矿浸出的影响。结果表明,随着盐酸和氯化铝的浓度和液固比的增大、反应时间的延长和反应温度的升高,精矿的浸出率逐渐增大,得到的优化浸出工艺条件如下:HCl和AlCl3浓度分别为4.0 mol/L和1.5 mol/L,液固比为20 mL/g,搅拌速度为300 r/min,温度为85℃,时间为90 min。SEM-EDS及动力学分析结果表明,精矿浸出过程符合一种受固体颗粒表面的界面交换和固膜扩散混合控制的新缩小核模型,表观活化能为35.3 kJ/mol,阿伦尼乌斯常数k0=419.95,反应级数a,b和c分别为1.265,1.208和1.22,通过计算推导出反应动力学方程。
採用氯化鋁鹽痠體繫配閤浸齣包頭混閤稀土精礦,併對浸齣過程動力學進行研究,浸齣過程主要攷察鹽痠和氯化鋁的濃度、液固比、攪拌速度、溫度及反應時間對精礦浸齣的影響。結果錶明,隨著鹽痠和氯化鋁的濃度和液固比的增大、反應時間的延長和反應溫度的升高,精礦的浸齣率逐漸增大,得到的優化浸齣工藝條件如下:HCl和AlCl3濃度分彆為4.0 mol/L和1.5 mol/L,液固比為20 mL/g,攪拌速度為300 r/min,溫度為85℃,時間為90 min。SEM-EDS及動力學分析結果錶明,精礦浸齣過程符閤一種受固體顆粒錶麵的界麵交換和固膜擴散混閤控製的新縮小覈模型,錶觀活化能為35.3 kJ/mol,阿倫尼烏斯常數k0=419.95,反應級數a,b和c分彆為1.265,1.208和1.22,通過計算推導齣反應動力學方程。
채용록화려염산체계배합침출포두혼합희토정광,병대침출과정동역학진행연구,침출과정주요고찰염산화록화려적농도、액고비、교반속도、온도급반응시간대정광침출적영향。결과표명,수착염산화록화려적농도화액고비적증대、반응시간적연장화반응온도적승고,정광적침출솔축점증대,득도적우화침출공예조건여하:HCl화AlCl3농도분별위4.0 mol/L화1.5 mol/L,액고비위20 mL/g,교반속도위300 r/min,온도위85℃,시간위90 min。SEM-EDS급동역학분석결과표명,정광침출과정부합일충수고체과립표면적계면교환화고막확산혼합공제적신축소핵모형,표관활화능위35.3 kJ/mol,아륜니오사상수k0=419.95,반응급수a,b화c분별위1.265,1.208화1.22,통과계산추도출반응동역학방정。
The complex leaching kinetics of Baotou mixed rare earth concentrate in HCl-AlCl3 solution was investigated. The effects of HCl concentration, AlCl3 concentration, liquid to solid ratio, stirring speed, temperature and reaction time were investigated. The results indicate that the concentrate leaching ratio increases with increasing the HCl and AlCl3 concentrations, liquid to solid ratio, temperature and reaction time. The optimal conditions are as follows:concentrations of HCl and AlCl3 are 4.0 mol/L and 1.5 mol/L, respectively, the liquid to solid ratio is 20 mL/g, the stirring speed is 300 r/min, temperature is 85 ℃, reaction time is 90 min. The SEM-EDS and kinetic analysis show that the concentrate leaching conforms with a new shrinking core model, in which both the interfacial transfer and diffusion through the product layer affect the reaction rate. The apparent activation energy is 35.3 kJ/mol, the Arrhenius constant k0 is 419.95, and the reaction series a, b, c are 1.27, 1.21 and 1.22, respectively. A kinetic equation was derived to describe the process.