首页 | 本学科首页   官方微博 | 高级检索  
     

制备高品质磷石膏的湿法磷酸新工艺的开发
引用本文:曾亚平,党亚固,费德君.制备高品质磷石膏的湿法磷酸新工艺的开发[J].化工进展,2015,34(Z1):167-172.
作者姓名:曾亚平  党亚固  费德君
作者单位:四川大学化学工程学院, 四川 成都 610065
摘    要:采用三级磷酸逆流萃取,然后加硫酸结晶的方法制备出高品质的磷酸和磷石膏。利用单因素实验法考察了温度、液固比、反应时间以及硫酸的用量对P2O5和各杂质萃取率的影响;通过实验确定最佳反应温度90℃,最佳反应时间2h,最佳液固比12:1,第三级硫酸的最佳用量为1.2%;萃取率达到98%以上;产品磷酸中的杂质CaO、Al2O3、Fe2O3、MgO含量分别下降到0.29%、0.11%、0.24%、0.431%;制备出白色的磷石膏,所得石膏采用水热法制备出晶形好和长径比较大的晶须;此法能运用到其他低品位的矿,适应性强,能够实现经济附加值,有广阔的推广前景。

关 键 词:逆流萃取  磷酸  石膏  晶须  

Development of the new wet phosphoric process of preparing high-quality phosphogypsum
ZENG Yaping,DANG Yagu,FEI Dejun.Development of the new wet phosphoric process of preparing high-quality phosphogypsum[J].Chemical Industry and Engineering Progress,2015,34(Z1):167-172.
Authors:ZENG Yaping  DANG Yagu  FEI Dejun
Affiliation:School of Chemical Engineering, Sichuan University, Chengdu 610065, Sichuan, China
Abstract:By level 3 phosphoric acid reflux extraction, then add sulfate crystallization method to make high quality phosphoric acid and phosphorus gypsum.Using the method of single factor experiment investigates the temperature, solid-liquid ratio, reaction time and the amount of sulfuric acid influence on extraction rate of P2O5 and each impurity. Determined by experiment, the best reaction temperature was 90℃, the best reaction time was 2h, best liquid-solid ratio was 12:1 and in the third level, the best dosage of sulfuric acid was 1.2%; Extraction rate reached 98% or more. The impurity in the phosphoric acid product,content of CaO, Al2O3, Fe2O3, MgO dropped respectively to 0.29%, 0.11%, 0.24% and 0.431%; Prepare white phosphorus gypsum, by hydrothermal method to make good crystal shape and length to diameter was larger whisker. This method can apply to other low grade ore, has strong adaptability, and can realize the economic value added with broad prospects for promotion.
Keywords:counter-current extraction  phosphoric acid  gypsum  whisker  
本文献已被 CNKI 万方数据 等数据库收录!
点击此处可从《化工进展》浏览原始摘要信息
点击此处可从《化工进展》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号