Chemical Industry and Engineering Progress ›› 2022, Vol. 41 ›› Issue (4): 2161-2170.DOI: 10.16085/j.issn.1000-6613.2021-0823

• Resources and environmental engineering • Previous Articles     Next Articles

Physical and chemical properties analysis of electrolytic manganese residue in different storage times

DENG Yaling1(), SHU Jiancheng1(), CHEN Mengjun1, LEI Tianya1, ZENG Xiangfei1, YANG Yong2, LIU Zuohua2   

  1. 1.School of Environment and Resource, Southwest University of Science and Technology, Mianyang 621000, Sichuan, China
    2.School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 401311, China
  • Received:2021-04-19 Revised:2021-06-21 Online:2022-04-25 Published:2022-04-23
  • Contact: SHU Jiancheng

不同堆存时间电解锰渣的理化特性分析

邓亚玲1(), 舒建成1(), 陈梦君1, 雷天涯1, 曾祥菲1, 杨勇2, 刘作华2   

  1. 1.西南科技大学环境与资源学院,四川 绵阳 621000
    2.重庆大学化学化工学院,重庆 401331
  • 通讯作者: 舒建成
  • 作者简介:邓亚玲(1997—),女,硕士研究生,研究方向为电解锰渣污染治理。E-mail:2533202812@qq.com
  • 基金资助:
    国家自然科学基金(21806132);国家重点研发计划(2018YFC1903500)

Abstract:

Electrolytic manganese residue (EMR) stored in the residue yard contains a large amount of manganese (Mn2+) and ammonia nitrogen (NH4+-N), which can easily migrate and pollute the surrounding environment. Therefore, the physical and chemical properties of EMR with different storage time (3 months to 10 years), such as pH, water content, conductivity, total metal content, leaching toxicity, chemical morphology and phase structure, were systematically studied. The phase composition, micro morphology and surface electronic valence of EMR with different storage time were analyzed by XRD, SEM and XPS. The results showed that with the storage time increased, pH, the water content, electrical conductivity and the contents of soluble Mn2+, Ca2+, Mg2+, Se4+ and NH4+-N decreased. Exchangeable and carbonates bound Mn were the main forms of Mn loss. EMR stored for 10 years still had a great risk of environmental pollution. The total amount of Cu, Cr, Cd, Pb, and Zn far exceeded the background value of Guangxi soil. The leaching concentration of Se4+ was 11 times of the concentration limit in 《Identification standards for hazardous wastes—Identification for extraction toxicity》 (GB 5085.3—2007). The leaching concentration of Mn2+ and NH4+-N were 102 times and 45 times of the first class standard limit of 《Integrated wastewater discharge standard》 (GB/T 8978—1996). The main forms of Mn2+ and NH4+-N in EMR with different storage time were (NH4)(Mn,Ca,Mg)PO4·H2O, (NH4)2SO4, MnSO4·H2O, MnCO3, Mn2O3 and MnO2. Iron-containing phases mainly included FeS2, FeOOH, Fe3O4 and Fe2O3. And it also contained clay minerals, including Al4(OH)8(Si4O10), Al2Mg4(OH)12(CO3)·3H2O and KAl(SO4)2·12H2O. In addition, with increasing storage time, the average pore size of EMR decreased, and the phenomenon of crisscross inclusion of massive, columnar and ball like particles increased. The Fe(OH)3 colloid particles gradually transformed into FeOOH, Fe2O3 and other iron-containing phases. The research results provided basic theoretical support for the harmless treatment and resource utilization of EMR.

Key words: electrolytic manganese residue, physical and chemical properties, storage times, manganese, ammonia nitrogen

摘要:

渣场堆存的电解锰渣中含有大量易迁移的锰和氨氮,极易污染周边环境。本文系统研究了不同堆存时间(3个月~10年)电解锰渣的pH、含水率、电导率、金属总量、浸出毒性和化学形态等理化特性,采用X射线衍射(XRD)、扫描电子显微镜(SEM)、能谱仪(EDS)以及X射线光电子能谱(XPS)等分析手段,探察电解锰渣在不同堆存时间下的物相组成、微观形貌、表面电子价态等变化规律。研究结果表明,随着堆存时间增加,锰渣的pH、含水率和电导率下降,可溶性Mn2+、Ca2+、Mg2+、Se4+和NH4+-N浓度降低,其中可交换态和碳酸盐结合态的Mn是Mn元素流失的主要形态。同时,堆存10年的电解锰渣仍存在较大的环境污染风险,其中电解锰渣中的Cu、Cr、Cd、Pb、Zn等金属总量远超广西土壤背景值,Se4+的浸出浓度是《危险废物鉴别标准 浸出毒性鉴别》(GB 5085.3—2007)中浓度限值的11倍,Mn2+和NH4+-N的浸出浓度是《污水综合排放标准》(GB/T 8978—1996)一级标准限值的102倍和45倍。不同堆存时间的电解锰渣中锰和氨氮主要以(NH4)(Mn,Ca,Mg)PO4·H2O、(NH4)2SO4、MnSO4·H2O、MnCO3、Mn2O3、MnO2等物相存在,含铁物相主要包括FeS2、FeOOH、Fe3O4和Fe2O3等,且电解锰渣中还含有Al4(OH)8(Si4O10)、Al2Mg4(OH)12(CO3)·3H2O和KAl(SO4)2·12H2O等黏土矿物。此外,随着堆存时间的增加,电解锰渣的平均孔径减小,块状、柱状和绒球形的电解锰渣颗粒交错包裹现象增加,同时Fe(OH)3胶体颗粒也逐渐转变成FeOOH、Fe2O3等含铁物相。本研究成果为电解锰渣无害化处理与资源化利用提供了基础理论支持。

关键词: 电解锰渣, 理化特性, 堆存时间, 锰, 氨氮

CLC Number: 

京ICP备12046843号-2;京公网安备 11010102001994号
Copyright © Chemical Industry and Engineering Progress, All Rights Reserved.
E-mail: hgjz@cip.com.cn
Powered by Beijing Magtech Co. Ltd