首页  |  本刊简介  |  编委会  |  投稿须知  |  订阅与联系  |  微信  |  出版道德声明  |  Ei收录本刊数据  |  封面
化学沉淀分离-置换法提纯Al13的工艺研究
摘要点击 1337  全文点击 1533  投稿时间:2006-01-23  修订日期:2006-04-01
查看HTML全文 查看全文  查看/发表评论  下载PDF阅读器
中文关键词  聚合氯化铝  Al13  分离提纯
英文关键词  polyaluminum chloride  Al13  separation
作者单位
李国红 中国科学院生态环境研究中心环境水质学国家重点实验室北京100085 
石宝友 中国科学院生态环境研究中心环境水质学国家重点实验室北京100085 
王东升 中国科学院生态环境研究中心环境水质学国家重点实验室北京100085 
崔亚莉 中国地质大学(北京)水资源与环境学院北京100083 
中文摘要
      采用AlCl3溶液和Na2CO3粉末在不同温度下制备了不同浓度的聚合氯化铝(PACl). 以选定的中等浓度、高Al13含量的PACl为原液,研究了Al13与硫酸盐沉淀反应过程中SO4/Al摩尔比、反应体系起始总铝浓度的影响以及Al13硫酸盐与Ba(NO3)2置换反应过程中的Ba/SO4摩尔比、超声、温度等因素的影响. 实验结果表明,在制备温度为50℃条件下,浓度在0.4~0.6 mol/L范围的PACl含有较高的Al13. 沉淀分离反应的最佳SO4/Al摩尔比为0.6∶1;生成的 Al13硫酸盐沉淀物为正四面体状晶体. 在Al13硫酸盐与Ba(NO3)2溶液置换反应过程中,Ba/SO4的最佳摩尔比为1∶1,反应温度及超声作用对置换反应的影响较小;提高Ba(NO3)2的起始浓度可以得到相应较高浓度的纯化Al13溶液. 所得Al13纯度的统计平均值为92.1%.
英文摘要
      PACls with different concentrations were prepared by adding sodium carbonate powder into AlCl3 solution. Medium concentration and high Al13 content of PACl was chosen to carry out Al13 separation processes. The influences of SO4/Al molar ratio and the initial total Al concentration on the precipitation reactions of sulfate with different Al species were investigated. The factors influencing the metathesis reaction between solid Al13-SO4 and Ba(NO3)2 were evaluated. Results showed that high Al13 PACl could be obtained at the medium high concentration range of 0.4~0.6 mol/L, the optimum SO4/Al ratio was 0.6∶1 for precipitation- separation of Al13, Al13-SO4 precipitates were mostly consisted of tetrahedral crystals. During the metathesis reaction, Ba/SO4 molar ratio of 1∶1 is the optimal value. Small range temperature variation and ultrasonic action had no marked influence on metathesis reaction rate and final Al13 concentration. Higher initial Ba(NO3)2 concentration could produce higher concentration Al13 accordingly. The purity of Al13 solution could be reached to 92.1% statistically.

您是第53213745位访客
主办单位:中国科学院生态环境研究中心 单位地址:北京市海淀区双清路18号
电话:010-62941102 邮编:100085 E-mail: hjkx@rcees.ac.cn
本系统由北京勤云科技发展有限公司设计  京ICP备05002858号-2