首页|钼焙砂氨浸过程中钾的释放动力学研究

钼焙砂氨浸过程中钾的释放动力学研究

扫码查看
随着低钾钼产品的广泛应用,企业对钼酸铵中的钾含量提出了越来越严苛的要求。氨浸作为钼酸铵生产的关键工艺,对钾的释放行为及产品质量都有十分重要的影响。以钼焙砂为实验原料,分析了钼酸铵生产过程中影响钾浸出的主要因素,并通过电感耦合等离子光谱(ICP)、X射线光电子能谱(XPS)、矿物解离分析仪(MLA)等方法研究了钾在钼酸铵生产过程中的释放动力学规律及其影响机制。结果发现:浸出时间、温度、固液比、原料粒度等都会对钾的浸出过程产生明显的影响;对钼酸铵降钾最适宜的条件为:温度为30 ℃,固液比为1∶5,钼焙砂粒径范围为150~178 μm,氨水质量分数为20%。此外,钾的释放动力学研究表明钼焙砂氨浸前期为离子钾的快速溶解过程,主要以KCl,K2SiF6的离子交换反应为主,该阶段符合Elovich模型,浸出活化能较小,为4。96kJ·mol-1;钼焙砂氨浸后期主要为矿物钾尤其是正长石和云母中钾的浸出释放过程,钾在该阶段的释放速率较慢,且受温度、固液比及粒度等条件的影响较大,该过程符合双常数模型,此阶段浸出活化能较大,为101。49 kJ·mol-1。
Release Kinetics of Potassium during Ammonia Leaching of Molybdenum Calcine
In addition to being used as an additive for steelmaking,molybdenum is also widely used in petrochemical industry,electrical and electronic technology,metallurgical machinery,medicine,agriculture and other fields.With the wide application of low potassium molybdenum products in photoelectric information,medical and other fields,enterprises have put forward more and more stringent requirements for potassium content in ammonium molybdate.Ammonium molybdate,as the raw material for the production of low potassium molybdenum products,is the precursor for the production of molybdenum powder and molybdenum metal products,and is also widely used in chemical reagents,catalysts,flame retardants and other aspects.Its potassium content directly affects or even determines the quality of follow-up molybdenum products.Therefore,reducing the potassium content in ammonium molybdate is critical to the production of low potassium high-quality molybdenum products.Ammonia leaching,as the key process of ammonium molybdate production,has a very important impact on the release behavior of potassium and product quality.In this paper,the main factors affecting potassium leaching in the production of ammonium molybdate were analyzed in sections with molybdenum calcine as the experimental material,and the release kinetics of potassium in the production of ammonium molybdate and its influence mechanism were studied by means of inductively coupled plasma(ICP),X-ray photoelectron spectroscopy(XPS),mineral quantitative analysis system(MLA),scanning electron microscopy(SEM)and energy dispersive spectroscopy(EDS).The main process of potassium release,the types of potassium bearing minerals and the transformation law in molybdenum calcine samples were systematically analyzed.Potassium containing minerals were bound in the mineral lattice by covalent bonds or are deeply bound by the lattice structure.The analysis results showed that although water washing could effectively remove most potassium ions in molybdenum calcine,a small part of potassium ions was still adsorbed on the surface of molybdenum calcine particles and released into solution during the ammonia leaching and dissolution of MoO3.The occurrence forms of potassium in the washed molybdenum calcine were potassium aluminosilicate,K2SiF6 and KCl.The total amount of potassium minerals decreased by 32.1%,which proved that potassium minerals also participated in the reaction.The main potassium minerals are orthoclase,illite,mica and barium ferrite mica.Potassium was released from the experimental samples through ion exchange and mineral decomposition.The mineral dissolution was mainly the release process of potassium in orthoclase and mica.Barite and illite released little potassium in ammonia,and orthoclase released more potassium than mica.In addition,the influences of leaching temperature,ratio of solid to liquid,particle size of raw materials and leaching time on the leaching process were discussed to obtain the best leaching conditions.The result showed that the release of potassium during ammonia leaching of molybdenum calcine could be divided into two stages:The first stage was the rapid dissolution reaction process of residual potassium ions in molybdenum calcine.At this time,the release reaction rate of potassium was fast,mainly concentrated in the first 35 min,and the release rate of potassium was large.The second stage was the release process of mineral potassium in molybdenum calcine.The release rate of potassium was relatively slow and the release amount was small.On the basis of analyzing the release behavior of potassium element,the optimum technological conditions of ammonia leaching of molybdenum calcine were determined.The results showed that the leaching time,temperature,solid-liquid ratio,raw material particle size,etc.would have a significant impact on the potassium leaching process.The most appropriate conditions for potassium reduction of ammonium molybdate were:temperature of 30 ℃,solid-liquid ratio of 1∶5,the particle size range of molybdenum calcine of 150~178 μm,and the concentration of ammonia water of 20%.In addition,the study of potassium release kinetics showed that the early stage of ammonia leaching of molybdenum calcine was a rapid dissolution process of ionic potassium,mainly the ion exchange reaction of KCl and K2SiF6.This stage conformed to Elovich model,and the leaching activation energy was 4.96 kJ·mol-1.The later stage of ammonia leaching of molybdenum calcine was mainly the release process of mineral potassium,especially potassium in orthoclase and mica.The release rate of potassium in this stage was slow,and it was greatly affected by temperature,solid-liquid ratio,particle size and other conditions.This process conformed to the double constant model,and the activation energy of leaching in this stage was 101.49 kJ·mol-1.The research results focused on the potassium leaching behavior of two stages in the ammonium molybdate leaching process,which could provide theoretical support for reducing the potassium content in ammonium molybdate products,so as to facilitate the preparation of ammonium molybdate with uniform particle size,intact grains and low potassium content,and effectively improve the product quality.

molybdenum calcineammonia leachingpotassium releasedynamicspotassium bearing mineral

刘起航、赵晓微、田顺治、冯卫国、刘东新

展开 >

西安建筑科技大学冶金工程学院,陕西西安 710055

陕西省冶金工程技术研究中心,陕西西安 710055

金堆城钼业股份有限公司,陕西西安 710077

钼焙砂 氨浸 钾释放 浸出动力学 含钾矿物

2024

稀有金属
北京有色金属研究总院

稀有金属

CSTPCD北大核心
影响因子:1.483
ISSN:0258-7076
年,卷(期):2024.48(11)