P507-HCl-酒石酸体系萃取分离轻稀土元素的基础研究
本文关键词: P507 酒石酸 分配比 分离系数 萃取容量 出处:《天津大学》2015年硕士论文 论文类型:学位论文
【摘要】:稀土行业的发展愈来愈快,其应用也变得日趋广泛,稀土元素已成为各国的重要战略资源。分离稀土元素的方法种类繁多,如今我国工业分离高纯单一的稀土元素的方法有很多,绝大多数采用皂化的P204或P507等酸性磷萃取剂分离稀土元素,该方法虽然萃取性能好,但有一个明显的弊端就是会产生大量的氨氮废水,对环境污染较为严重。针对此缺点,本论文通过研究在有机萃取剂P507中加入一种名为酒石酸的配合剂,研究了在该体系下的三个重要参数分配比、分离系数、萃取饱和容量与酸度、酒石酸浓度和稀土浓度之间的相互关系,并与不含酒石酸的P507—盐酸体系的分离效果进行对比,最后研究了该体系下轻稀土从有机相到水相的反萃过程。本文采用单级萃取实验,研究了在不同的稀土浓度、酸度和酒石酸浓度条件下,该体系四种轻稀土元素的分配比、分离系数和萃取饱和容量的变化情况。主要结论如下:当料液酸度PH值控制在1.0、酒石酸浓度和稀土浓度均为0.25mol/L、萃取剂浓度为1.5mol/L时,分配比以及分离系数达到最大,分别达到DLa=0.1966、DCe=0.7781、DPr=1.6215和DNd=2.4899,βCe/La=4.08、βPr/ce=1.98和βNd/Pr=1.62;并且随着酒石酸浓度的升高,P507萃取四种轻稀土的饱和容量也逐渐增大,可以达到29.7g/L,比单一盐酸体系提高约50%。最后做了稀土的反萃实验,串级反萃模拟实验结果表明,当反萃盐酸浓度5mol/L,在相比O/A=2:1下,经过5级反萃后,稀土的反萃率可达到98%以上,并且出口稀土浓度较大,出口酸度较低,负载有机相中残留的酸量较小,约为0.8mol/L,反萃效果好。P507—HCI—酒石酸体系无需皂化过程,工艺简单,萃取效果较好、分离系数高、反萃容易。由于该萃取体系不需要加入皂化剂,可大大降低氨氮废水的产生,同时节约了成本,是一项颇具特色的稀土萃取分离工艺。
[Abstract]:The rare earth industry is developing more and more rapidly, and its application is becoming more and more extensive. Rare earth elements have become an important strategic resource in various countries. There are many methods of separating rare earth elements. Nowadays, there are many industrial methods for separating high purity and single rare earth elements in our country, most of them are separated by saponification acid phosphorus extractants such as P204 or P507, although this method has good extraction performance. However, there is an obvious drawback that a large amount of ammonia-nitrogen wastewater will be produced, which will cause serious environmental pollution. In view of this shortcoming, this paper studied the addition of a complex agent called tartaric acid to the organic extractant P507. The relationship between the distribution ratio of three important parameters, separation coefficient, extraction saturation capacity and acidity, tartaric acid concentration and rare earth concentration in this system was studied, and the results were compared with those of P507-hydrochloric acid system without tartaric acid. Finally, the stripping process of light rare earth from organic phase to water phase in this system was studied. The distribution ratio of four light rare earth elements in this system was studied under different rare earth concentration, acidity and tartaric acid concentration by single stage extraction experiment. The main conclusions are as follows: when the pH value of feed liquid is 1.0, the concentration of tartaric acid and rare earth is 0.25 mol / L, and the concentration of extractant is 1.5 mol / L, the distribution ratio and separation coefficient reach the maximum when the pH value of feed solution is 1.0, the concentration of tartaric acid and rare earth is 0.25 mol / L, and the concentration of extractant is 1.5 mol / L. The saturated capacity of four kinds of light rare earths was gradually increased with the increase of tartaric acid concentration, and the saturation capacity of four kinds of light rare earths was gradually increased, reaching 29.7 g / L, which was about 500.5% higher than that of the single hydrochloric acid system. Finally, the extraction capacity of 尾 Pr/ce=1.98 and 尾 NdR was 4.08, 尾 Pr/ce=1.98 and 尾 Ndrr 1.62with the increase of the concentration of tartaric acid, and the saturation capacity of the four kinds of light rare earths was gradually increased to 29.7 g / L, which was about 50g / L higher than that of the single hydrochloric acid system, with the increase of the concentration of tartaric acid. The simulation results of cascade stripping experiments show that when the concentration of hydrochloric acid is 5 mol / L, when compared with O / A 2: 1, the stripping rate of rare earth can reach more than 98%, and the export concentration of rare earth is higher and the export acidity is lower than that of O / A (2: 1). The residual acid content in the loaded organic phase is about 0.8 mol / L, the stripping effect is good. P507-HCI- tartaric acid system does not need saponification process, the process is simple, the extraction effect is better, the separation coefficient is high, the stripping is easy, because the extraction system does not need to add saponification agent, It can greatly reduce the production of ammonia nitrogen wastewater and save the cost. It is a characteristic rare earth extraction and separation process.
【学位授予单位】:天津大学
【学位级别】:硕士
【学位授予年份】:2015
【分类号】:TQ133.3;TQ028.32
【参考文献】
相关期刊论文 前10条
1 杨幼明;邓声华;蓝桥发;聂华平;叶信宇;;P507-N235体系稀土萃取分离性能研究[J];有色金属科学与工程;2013年03期
2 苏永祥;孙跃枝;;双水相萃取技术的研究现状及应用[J];焦作师范高等专科学校学报;2007年03期
3 胡元钧;;萃取色层在稀土分离中的应用[J];科技情报开发与经济;2007年19期
4 黄光荣;活泼;戴德慧;蒋家新;;反胶团萃取嗜热芽孢杆菌HS08发酵液中胞外蛋白酶研究[J];中国计量学院学报;2007年02期
5 吕玄文;梁敏思;党志;杨琛;;鱼塘沉积物中氯霉素的超声萃取、净化与测定[J];农业环境科学学报;2007年03期
6 林郑和;;超临界流体萃取技术在茶叶研究中的应用[J];茶叶科学技术;2007年02期
7 周含英;黄益鸿;王盛才;吴小平;邹辉;罗岳平;;微波萃取-气相色谱法测定土壤中六六六、滴滴涕[J];光谱实验室;2007年02期
8 侯彩霞;李淑芬;;挥发油的超临界流体萃取与分离进展[J];化工进展;2007年01期
9 吕金海;舒孝顺;高中洪;杨祥良;;菝葜总皂苷元超声萃取研究[J];中国中药杂志;2007年02期
10 王力;王琳玲;赵天珍;赵柳青;黄卫红;陆晓华;;超声萃取沉积物中六氯苯的研究[J];分析科学学报;2006年06期
相关博士学位论文 前1条
1 车丽萍;乳状液膜技术回收处理白云鄂博稀土矿中钍的研究[D];武汉理工大学;2006年
相关硕士学位论文 前2条
1 邓声华;P507-N235体系稀土无皂化萃取分离关键技术研究[D];江西理工大学;2012年
2 张磊;双水相体系提取废弃印刷线路板中的金[D];东华大学;2007年
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