| 451 | 12 | 20 |
| 下载次数 | 被引频次 | 阅读次数 |
通过模拟铅锌尾矿环境中酸性矿山废水、选矿废水(含乙基黄药)连续淋溶铅锌尾矿试验,研究渗滤液和脉石颗粒变化,并以此分析自然中和与沉淀吸附金属的地球化学过程,对淋溶后矿物颗粒表面进行表征。结果表明,当铁离子、铅离子和镉离子含量分别为200、20、5mg/L的酸性淋溶液与乙基黄药浓度为100mg/L的选矿废水经过淋溶柱后,由于碳酸盐的自中和特性,渗滤液的pH为7~8;渗滤液中镉、铅离子含量均小于0.05mg/L,并且渗滤液中乙基黄药的去除率为99%以上。矿物颗粒表征结果表明,乙基黄药没有影响铁矿物的形成,脉石颗粒表面覆盖了Ca(OH)2、CaSO4亲水性钙膜和铁矿物,并且铁矿物会吸附铅离子和镉离子。
Abstract:Changes of leachate and gangue particles were studied to analyze geochemical processes of natural neutralization and precipitation of adsorbed metals through simulating continuous leaching of lead-zinc tailings with acid mine wastewater and ethylxanthate-bearing beneficiation wastewater.Surfaces of mineral particles after leaching were characterized.The results show that when acidic leaching solution with iron,lead and cadmium ion content of 200,20,and 5 mg/L respectively,and beneficiation wastewater with ethyl xanthate concentration of 100 mg/L pass the leaching column,pH of leachate is 7~8 due to selfneutralization characteristics of carbonate,content of cadmium and lead ions in leachate is less than0.05 mg/L,and removal rate of ethyl xanthate in leachate is 99% above.The results of mineral particle characterization show that ethyl xanthate does not affect formation of iron minerals.Surface of gangue particles are covered by Ca(OH)2,CaSO4 hydrophilic calcium film and iron minerals,and iron minerals adsorb lead and cadmium ions.
[1]NLEYA Y,SIMATE G S,NDLOVU S.Sustainability assessment of the recovery and utilization of acid from acid mine drainage[J].Journal of Cleaner Production,2016,113:17-27.
[2]MOODLEY I,SHERIDAN C M,KAPPELMEYER U,et al.Environmentally sustainable acid mine drainage remediation:Research developments with a focus on waste/by-products[J].Minerals Engineering,2018,126:207-220.
[3]LARSSON M L,HOLMGREN A,FORSLING W.Xanthate adsorbed on ZnS studied by polarized FTIRATR spectroscopy[J].Langmuir,2000,16(21):8129-8133.
[4]BAG B,DAS B,MISHRA B K.Geometrical optimization of xanthate collectors with copper ions and their response to flotation[J].Minerals Engineering,2011,24(8):760-765.
[5]LU J,ALAKANGAS L, WANHAINEN C. Metal mobilization under alkaline conditions in ash-covered tailings[J].Journal of Environmental Management,2014,139:38-49.
[6]SHU X H,DANG Z,ZHANG Q,et al.Passivation of metal-sulfide tailings by covalent coating[J].Minerals Engineering,2013,42:36-42.
[7]FORNASIERO D,MONTALTI M,RALSTON J.Kinetics of adsorption of ethyl xanthate on pyrrhotite:In situ UV and infrared spectroscopic studies[J].Journal of Colloid and Interface Science,1995,172(2):467-478.
[8]CHEN X,HU Y,PENG H,et al.Degradation of ethyl xanthate in flotation residues by hydrogen peroxide[J].Journal of Central South University,2015,22(2):495-501.
[9]BOILY J F,GASSMAN P L,PERETYAZHKO T,et al.FTIR spectral components of schwertmannite[J].Environmental Science&Technology,2010,44(4):1185-1190.
[10]VITHANA C L,SULLIVAN L A,BURTON E D,et al.Stability of schwertmannite and jarosite in an acidic landscape:Prolonged field incubation[J].Geoderma,2015,239:47-57.
[11]WU S J,LU J W,DIMG Z C,et al.Cr(VI)removal by mesoporous FeOOH polymorphs:Performance and mechanism[J].RSC Advances,2016,6(85):82118-82130.
[12]ZENG L Y,REN W Z,ZHENG J J,et al.Synthesis of water-soluble FeOOH nanospindles and their performance for magnetic resonance imaging[J].Applied Surface Science,2012,258(7):2570-2575.
[13]MOURA K O,LIMA R J S,COELHO A A,et al.Tuning the surface anisotropy in Fe-doped NiO nanoparticles[J].Nanoscale,2014,6(1):352-357.
[14]BARIK R,JENA B K,MOHAPATRA M.Metal doped mesoporous FeOOH nanorods for high performance supercapacitors[J].RSC Advances,2017,7(77):49083-49090.
[15]YANG T T,MENG L R,HAN S W,et al.Simultaneous reductive and sorptive removal of Cr(VI)by activated carbon supportedβ-FeOOH[J].RSC Advances,2017,7(55):34687-34693.
[16]WANG Y,ZHANG Y,FENG Y C,et al.XPS study on changes of lead on the channel surface of microchannel plate reduced by hydrogen[C]//IOP Conference Series:Materials Science and Engineering.IOP Publishing,2019,490(2):022067.
[17]YUAN X J,MA X H,LIAO J,et al.Low-pollution and controllable selective-area deposition of a CdS buffering layer on CIGS solar cells by a photochemical technique[J].ACS Sustainable Chemistry&Engineering,2017,5(8):7325-7333.
基本信息:
中图分类号:X753
引用信息:
[1]蒋莉蓉,曹长春,蔡维炯.酸性矿山废水与含黄药选矿废水淋溶铅锌尾矿试验[J].有色金属(冶炼部分),2020(01):84-90.
基金信息:
广西科技计划重大专项(桂科重14124001-4); 广西环境污染控制理论与技术重点实验室项目(H2015123111)
2020-01-12
2020-01-12