4.8 Article

Enhanced chitosan beads-supported Fe0-nanoparticles for removal of heavy metals from electroplating wastewater in permeable reactive barriers

期刊

WATER RESEARCH
卷 47, 期 17, 页码 6691-6700

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.watres.2013.09.006

关键词

Nanoscale zero-valent iron (NZVI); Permeable reactive barriers (PRBs); Ethylene glycol diglycidyl; ether (EGDE); Heavy metals; Electroplating wastewater

资金

  1. National Science & Technology Pillar Program [2012BAC07B02]
  2. National Natural Science Foundation of China [21307090]
  3. University Science & Technology Development Project of Tianjin [20110528]
  4. Program for New Century Excellent Talents in University [NCET-10-0954]
  5. Natural Science Foundation of Tianjin [10SYSYJC27400]
  6. Foundation of Tianjin Normal University [5RL109, 52XQ1104]
  7. Opening Fund of Tianjin Key Laboratory of Water Resources and Environment [YF11700102]

向作者/读者索取更多资源

The removal of heavy metals from electroplating wastewater is a matter of paramount importance due to their high toxicity causing major environmental pollution problems. Nanoscale zero-valent iron (NZVI) became more effective to remove heavy metals from electroplating wastewater when enhanced chitosan (CS) beads were introduced as a support material in permeable reactive barriers (PRBs). The removal rate of Cr (VI) decreased with an increase of pH and initial Cr (VI) concentration. However, the removal rates of Cu (II), Cd (II) and Pb (II) increased with an increase of pH while decreased with an increase of their initial concentrations. The initial concentrations of heavy metals showed an effect on their removal sequence. Scanning electron microscope images showed that CS-NZVI beads enhanced by ethylene glycol diglycidyl ether (EGDE) had a loose and porous surface with a nucleus-shell structure. The pore size of the nucleus ranged from 19.2 to 138.6 mu m with an average aperture size of around 58.6 mu m. The shell showed a tube structure and electroplating wastewaters may reach NZVI through these tubes. X-ray photoelectron spectroscope (XPS) demonstrated that the reduction of Cr (VI) to Cr (III) was complete in less than 2 h. Cu (II) and Pb (II) were removed via predominant reduction and auxiliary adsorption. However, main adsorption and auxiliary reduction worked for the removal of Cd (II). The removal rate of total Cr, Cu (II), Cd (II) and Pb (II) from actual electroplating wastewater was 89.4%, 98.9%, 94.9% and 99.4%, respectively. The findings revealed that EGDE-CS-NZVI-beads PRBs had the capacity to remediate actual electroplating wastewater and may become an effective and promising technology for in situ remediation of heavy metals. (C) 2013 Elsevier Ltd. All rights reserved.

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