首页> 外文期刊>Environmental Science & Technology >Effects of Ca~(2+) and Mg~(2+) on Defluoridation in the Electrocoagulation Process
【24h】

Effects of Ca~(2+) and Mg~(2+) on Defluoridation in the Electrocoagulation Process

机译:Ca〜(2+)和Mg〜(2+)对电凝过程中脱氟的影响

获取原文
获取原文并翻译 | 示例
       

摘要

Because aqueous ions can influence the defluoridation of the electrocoagulation (EC) process, the effects of Ca~(2+) and Mg~(2+) were investigated. The behaviors and mechanisms of EC defluoridation in Ca~(2+)-comaining systems were different from those in Mg~(2+)-containing systems. An increase in Ca~(2+) concentration improved the defluoridation efficiency (εF). but it could not change the optimal molar ratio of OH~- and F~- to A/~(3+) (r_(OH)+F). The highest εF can usually be obtained at (r_(OH)+F) = 3 for defluoridation. Only a small portion of Ca~(2+) entered into the flocs, and Ca~(2+) could not influence the mechanism of EC defluoridation. For the Mg~(2+)-containing system, the optimal (r_(OH)+F) increased with increasing Mg~(2+) concentration. The optimal r_(oh+f) was maintained at 3 after the Mg~(2+) concentration was corrected using the obtained correction coefficient of 03435. About 50% to 70% of the total Mg~(2+) entered into the flocs. From the XRD analysis, it was found that some Mg-AI-F layered double hydroxides (LDHs) were formed by Mg~(2+), F~-, and Al~(3+) during electrolysis. It is proposed for the first time that the formation of Mg-AI-F LDH is one of the mechanisms for EC defluoridation in systems containing both F~- and Mg~(2+).
机译:由于水离子会影响电凝过程的脱氟作用,因此研究了Ca〜(2+)和Mg〜(2+)的作用。含Ca〜(2+)的体系中EC脱氟的行为和机理与含Mg〜(2+)的体系中的EC脱氟的行为和机理不同。 Ca〜(2+)浓度的增加提高了脱氟效率(εF)。但是它不能改变OH〜-和F〜-与A /〜(3+)(r_(OH)+ F)的最佳摩尔比。对于脱氟,通常可以在(r_(OH)+ F)= 3的情况下获得最高εF。 Ca〜(2+)只有一小部分进入絮凝物中,而Ca〜(2+)不能影响EC的除氟机理。对于含Mg〜(2+)的体系,最佳(r_(OH)+ F)随着Mg〜(2+)浓度的增加而增加。使用获得的校正系数03435对Mg〜(2+)浓度进行校正后,最佳r_(oh + f)保持在3。大约有50%至70%的总Mg〜(2+)进入絮凝物。通过XRD分析发现,在电解过程中,Mg〜(2 +),F〜-和Al〜(3+)形成了一些Mg-Al-F层状双氢氧化物(LDHs)。首次提出,在同时含有F〜-和Mg〜(2+)的体系中,Mg-Al-F LDH的形成是EC脱氟的机制之一。

著录项

  • 来源
    《Environmental Science & Technology》 |2010年第23期|p.9112-9116|共5页
  • 作者单位

    Department of Environmental Engineering, Peking University,Beijing 100871, People's Republic of China,The Key Laboratory of Water and Sediment Sciences, Ministry of Education, Beijing 100871, People's Republic of China;

    Department of Environmental Engineering, Peking University,Beijing 100871, People's Republic of China,The Key Laboratory of Water and Sediment Sciences, Ministry of Education, Beijing 100871, People's Republic of China;

    Department of Environmental Engineering, Peking University,Beijing 100871, People's Republic of China,The Key Laboratory of Water and Sediment Sciences, Ministry of Education, Beijing 100871, People's Republic of China;

    Department of Environmental Engineering, Peking University,Beijing 100871, People's Republic of China,The Key Laboratory of Water and Sediment Sciences, Ministry of Education, Beijing 100871, People's Republic of China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 14:04:07

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号