Removal of nitrate from groundwater using the technology of electrodialysis and electrodeionization

被引:48
作者
Bi, Jingjing [1 ]
Peng, Changsheng [1 ]
Xu, Huizhen [1 ]
Ahmed, Abou-Shady [1 ]
机构
[1] Ocean Univ China, Coll Environm Sci & Engn, Qingdao, Peoples R China
关键词
Nitrate contamination; Electrodialysis; Electrodeionization; Water reuse; Regeneration;
D O I
10.5004/dwt.2011.2891
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
In this paper, the technical capabilities of a lab-scale electrodeionization (EDI) process and its basic technology electrodialysis (ED) process that used for removing NO(3)(-) from nitrate-contaminated groundwater were investigated. The EDI unit with three chambers (anode, diluted and cathode) was used; it utilized electricity to regenerate ion-exchange resins instead of chemicals. At first, the voltage-current (V-I) characteristic curves about the ED and EDI processes were studied, and then chose the optimum operating voltage which based on the curves. The effects of operational parameters (voltage, water flow rate and initial NO(3) -N concentration) on nitrate removal rate and concentration effect of ED and different ion-exchange resins, the proportion of anion and cation resins and the voltage used for regeneration of EDI were investigated. The results of ED showed that NO(3)(-)-N concentration could be reduced from initial 50-300 mg/l to 1-6 mg/l, with the removal rate 99% and the conductivity could be reduced to less than 10 mu s/cm. Under the conditions of equal (1-8 l/h) and unequal (1:1,2,3,4,5,6,7,8 l/h) water flow rate between concentrated and diluted water, the concentrated water could be reached to 2-5 times more than the initial water. The current efficiency and energy consumption was 17-34% and 0.-1.7 W.h/l, respectively. It was shown that ED was effective to NO(3)(-) removal and concentration. As to EDI process, the results showed that continuous electrodeionization could regenerate the resins effectively from simulated nitrate-contaminated water. Under the condition of 50 V as the regenerate voltage, after 90 h, the regeneration rate was as high as 60%. In addition, the NO(3)(-)-N concentration of the diluted water was reduced to 5 mg/l from initial 50 mg/l. As a fundamental technology of in-situ remediation for groundwater contamination, the process was proved to be feasible and provided foundation for further research.
引用
收藏
页码:394 / 401
页数:8
相关论文
共 13 条
  • [1] Cr(VI) removal by continuous electrodeionization: Study of its basic technologies
    Alvarado, L.
    Ramirez, A.
    Rodriguez-Torres, I.
    [J]. DESALINATION, 2009, 249 (01) : 423 - 428
  • [2] [Anonymous], 1484893 GBT
  • [3] Canter L.W., 1997, Nitrates in Groundwater
  • [4] Chen G., 2009, J HEBEI AGR SCI, V13, P90
  • [5] Kinetics of reductive denitrification by nanoscale zero-valent iron
    Choe, S
    Chang, YY
    Hwang, KY
    Khim, J
    [J]. CHEMOSPHERE, 2000, 41 (08) : 1307 - 1311
  • [6] Edtkea K., 1998, J MEMB, V151, P3
  • [7] Development of an electrodeionization process for removal of nitrate from drinking water - Part 1: Single-species testing
    Meyer, N
    Parker, WJ
    Van Geel, PJ
    Adiga, M
    [J]. DESALINATION, 2005, 175 (02) : 153 - 165
  • [8] [潘涌璋 PAN Yongzhang], 2008, [安徽农业科学, Journal of Anhui Agricultural Sciences], V36, P5147
  • [9] Reddy KR, 2009, ELECTROCHEMICAL REME, DOI 10.1002/9780470523650
  • [10] Electrokinetic remediation of clayey soils containing copper(II)-oxinate using humic acid as a surfactant
    Sawada, A
    Tanaka, S
    Fukushima, M
    Tatsumi, K
    [J]. JOURNAL OF HAZARDOUS MATERIALS, 2003, 96 (2-3) : 145 - 154