Study on the environmental durability of heavy metal contaminated soil remediated by enzyme induced carbonate precipitation

被引:0
|
作者
Bian Han-liang [1 ,2 ]
Ji Pei-rui [1 ]
Wang Jun-ling [3 ]
Zhang Xu-gang [4 ]
Xu Xiang-chun [1 ,2 ]
机构
[1] Henan Univ, Sch Civil Engn & Architecture, Kaifeng 475004, Henan, Peoples R China
[2] Henan Univ, Kaifeng Technol Res Ctr Engn Soil Modificat & Res, Kaifeng 475004, Henan, Peoples R China
[3] Scivic Engn Corp, Luoyang 471003, Henan, Peoples R China
[4] Second Construct Ltd Co, China Construct Engn Div 8, Jinan 250014, Shandong, Peoples R China
关键词
zinc and lead contaminated soil; enzyme induced carbonate precipitation (EICP); acid soaking; freeze-thaw test; rainfall test; CEMENTATION; SAND;
D O I
10.16285/j.rsm.2023.0992
中图分类号
P5 [地质学];
学科分类号
0709 ; 081803 ;
摘要
To explore the environmental durability of heavy metal contaminated soil remediated by enzyme induced carbonate precipitation (EICP) technology, acid soaking, freeze-thaw tests, and rainfall tests were carried out on the zinc and lead contaminated soil after EICP remediation, respectively. The durability and influence of the zinc and lead contaminated soil remediated by EICP technique under different environmental conditions and the corresponding influence regularity were discussed in this paper. The results showed that under different concentrations and types of acid solutions, the leaching amount of heavy metal ions in exchangeable and carbonate bound forms in the zinc and lead contaminated soil after EICP remediation decreased with pH value, with the content of ions in carbonate bound forms decreasing and the content of ions in exchangeable forms gradually increasing. It was also found that the stability in sulfuric acid solution was greater than that in nitric acid solution. As the number of freeze-thaw cycles increased, the leaching amount of exchangeable ions in the zinc and lead contaminated soil remediated by EICP technique increased, while the content of ions in the carbonate bound form reduced. Under the condition of heavy rain, Zn2+ and Pb2+ were mainly released within the first 20 minutes and migrated from top to bottom. All the results demonstrate that the heavy metal contaminated soil remediated by EICP technology has a good durability under acid soaking, freeze-thaw cycles, and heavy rain.
引用
收藏
页码:2779 / 2788
页数:10
相关论文
共 36 条
  • [1] Bioremediation of Pb-Contaminated Soil Based on Microbially Induced Calcite Precipitation
    Achal, Varenyam
    Pan, Xiangliang
    Zhang, Daoyong
    Fu, Qinglong
    [J]. JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, 2012, 22 (02) : 244 - 247
  • [2] [边汉亮 Bian Hanliang], 2022, [工业建筑, Industrial Construction], V52, P67
  • [3] Cao GH, 2022, ROCK SOIL MECH, V43, P2241, DOI 10.16285/j.rsm.2021.1839
  • [4] [陈莉薇 Chen Liwei], 2020, [安全与环境学报, Journal of Safety and Environment], V20, P735
  • [5] Spatial Distribution Characteristics and Pollution Evaluation of Heavy Metals in Arable Land Soil of China
    Chen W.-X.
    Li Q.
    Wang Z.
    Sun Z.-J.
    [J]. Huanjing Kexue/Environmental Science, 2020, 41 (06): : 2822 - 2833
  • [6] Cui M, 2022, ROCK SOIL MECH, V43, P3027, DOI 10.16285/j.rsm.2021.2157
  • [7] Microbially induced cementation to control sand response to undrained shear
    DeJong, Jason T.
    Fritzges, Michael B.
    Nusslein, Klaus
    [J]. JOURNAL OF GEOTECHNICAL AND GEOENVIRONMENTAL ENGINEERING, 2006, 132 (11) : 1381 - 1392
  • [8] Distribution of Heavy Metal Pollution in Surface Soil Samples in China: A Graphical Review
    Duan, Qiannan
    Lee, Jianchao
    Liu, Yansong
    Chen, Han
    Hu, Huanyu
    [J]. BULLETIN OF ENVIRONMENTAL CONTAMINATION AND TOXICOLOGY, 2016, 97 (03) : 303 - 309
  • [9] Enzyme-induced carbonate mineral precipitation for fugitive dust control
    Hamdan, N.
    Kavazanjian, E., Jr.
    [J]. GEOTECHNIQUE, 2016, 66 (07): : 546 - 555
  • [10] Microbial induced carbonate precipitation for immobilizing Pb contaminants: Toxic effects on bacterial activity and immobilization efficiency
    Jiang, Ning-Jun
    Liu, Rui
    Du, Yan-Jun
    Bi, Yu-Zhang
    [J]. SCIENCE OF THE TOTAL ENVIRONMENT, 2019, 672 : 722 - 731