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金属矿山 ›› 2026, Vol. 55 ›› Issue (3): 226-238.

• 安全与环保 • 上一篇    下一篇

PEM 电解技术对矿山酸性废水中( 类) 金属的处理效果

李丹霓1 毛启明2 魏建宏3 郭 靖1 卜心愿1 张彦勰4 罗 琳1   

  1. 1. 湖南农业大学环境与生态学院,湖南 长沙 410128;2. 中南大学资源加工与生物工程学院,湖南 长沙 410083;
    3. 湖南农业大学生物科学技术学院,湖南 长沙 410128;4. 吉首大学生物资源与环境科学学院,湖南 吉首 416000
  • 出版日期:2026-03-15 发布日期:2026-04-01
  • 通讯作者: 罗 琳(1969—),男,教授,博士,博士研究生导师。
  • 作者简介:李丹霓(1999—),女,硕士研究生。
  • 基金资助:
    国家自然科学基金项目(编号:42077380,U20A2080);湖南省自然科学基金项目(编号:2024JJ6524);湖南省重点研发计划项目(编号:
    2024AQ2006);湖南省研究生科研创新项目(编号:QL20230170)。

Treatment Effect of PEM Electrolysis Technology on Metal(loid)s in Acid Mine Drainage

LI Danni1 MAO Qiming2 WEI Jianhong3 GUO Jing1 BU Xinyuan1 ZHANG Yanxie4 LUO Lin1   

  1. 1. College of Environment and Ecology,Hunan Agricultural University,Changsha 410128,China;
    2. School of Minerals Processing and Bioengineering,Central South University,Changsha 410083,China;
    3. College of Biological Science and Technology,Hunan Agricultural University,Changsha 410128,China;
    4. College of Biology and Environmental Sciences,Jishou University,Jishou 416000,China
  • Online:2026-03-15 Published:2026-04-01

摘要: 采矿活动产生的矿山酸性废水(AMD)呈强酸性,含有高浓度的Fe2+ ,并伴有(类)金属污染。为实现
AMD 的高效处理,本研究建立了质子交换膜(PEM)电解系统。系统在最优条件下(铱钛网阳极,铂片阴极,15 g/ L
SO2-
4 ,60 mA)将pH 为2. 5~4. 5,Fe2+浓度为200~800 mg/ L,含50 mg/ L Fe3+(Mn2+ 、Cr3+ 、Cu2+ 、Zn2+或As5+ )的AMD 中
(类)金属浓度在290 min 内降至符合饮用水标准。其除Fe 效率与初始pH(2. 5~4. 5)正相关,与初始Fe2+浓度(200~
800 mg/ L)负相关。50 mg/ L Fe3+ 、Cu2+和Zn2+对其除Fe2+起抑制作用,Mn2+和Cr3+起促进作用,As5+无影响。产物表征
证明,AMD 中Fe2+初期部分被溶解氧氧化为(氢)氧化铁,部分水解为(氢)氧化亚铁,末期溶解再结晶为Fe3O4;Fe3+
Mn2+ 、Cr3+ 、Cu2+和Zn2+与Fe2+共沉淀为金属氧化物;As5+被铁矿物吸附。

Abstract: Acid Mine Drainage (AMD) generated from mining activities is strongly acidic,containing high concentrations
of Fe2+ along with metal(loid) pollutants. To efficiently treat AMD,a proton exchange membrane (PEM) electrolysis system
was developed. Under the optimal process parameters (iridium titanium mesh anode,platinum plate cathode,15 g/ L SO2-
4 ,60mA),this system reduced the metal(loid) concentrations in AMD with a pH of 2. 5~3. 5,an initial Fe2+ concentration of 200
~800 mg/ L,and containing 50 mg/ L of Fe3+ ,Mn2+ ,Cr3+ ,Cu2+ ,Zn2+ or As5+ to meet the drinking water standards within 290
min. The removal efficiency of Fe in AMD by PEM electrolysis technology was positively correlated with the initial pH (2. 5~
4. 5) and negatively correlated with the initial Fe2+ concentration (200 ~ 800 mg/ L). 50 mg/ L of Fe3+ ,Cu2+ ,and Zn2+ in
wastewater inhibited the removal of Fe,while Mn2+ and Cr3+ promoted it. As5+ showed no significant effect. Products characterization
showed that during the initial stage,part of the Fe2+ in the wastewater was oxidized by dissolved oxygen to (hydro) ferric
oxide,while another portion hydrolyzed to form (hydrogen) ferrous hydroxide. In the final stage,these intermediates dissolved
and recrystallized into Fe3O4;Fe3+ ,Mn2+ ,Cr3+ ,Cu2+ and Zn2+ co-precipitated with Fe2+ as mixed metal oxides;As5+ was
adsorbed onto the iron minerals formed.

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