Lab-scale simulation of the fate and transport of nano zero-valent iron in subsurface environments : aggregation, sedimentation, and contaminant desorption

Heavy metal removal using nano zero-valent iron (NZVI) has drawn growing attention due to the ease of application and high removal efficiency. However, uncertainties regarding its fate and transport in subsurface environments have raised concerns that require further exploration. In this study, aggr...

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Main Authors: Lo, Irene M. C., Mak, Mark S. H., Yin, Ke, Dong, Haoran, Rao, Pinhua
Other Authors: School of Civil and Environmental Engineering
Format: Article
Language:English
Published: 2013
Online Access:https://hdl.handle.net/10356/97154
http://hdl.handle.net/10220/11637
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-971542020-03-07T11:43:43Z Lab-scale simulation of the fate and transport of nano zero-valent iron in subsurface environments : aggregation, sedimentation, and contaminant desorption Lo, Irene M. C. Mak, Mark S. H. Yin, Ke Dong, Haoran Rao, Pinhua School of Civil and Environmental Engineering Residues and Resource Reclamation Centre Heavy metal removal using nano zero-valent iron (NZVI) has drawn growing attention due to the ease of application and high removal efficiency. However, uncertainties regarding its fate and transport in subsurface environments have raised concerns that require further exploration. In this study, aggregation, sedimentation, and Cr/As desorption of three types of NZVIs were investigated under various conditions. It was found that the aggregation behavior of the NZVIs differed from one another in regard to reaction time and ionic strength, associated with the respective critical size for sedimentation. Sedimentation of NZVIs was positively related to the concentrations and average particle sizes. The sedimentation kinetics of NZVI followed two concomitant processes, i.e., (1) direct sedimentation of larger particles, and (2) initial aggregation and then sedimentation of smaller particles. When loaded with Cr/As, NZVIs tended to deposit faster, possibly due to the precipitation of Cr/As onto the nanoparticle surfaces resulting in larger particle sizes. Moreover, desorption of Cr/As from Cr/As loaded NZVIs was detected in the presence of typical groundwater ions, as well as natural organic matter, and poses a potential risk to the subsurface environment. The desorption of Cr was linearly related to the release of iron ions, while As desorption was mitigated when the immobilization of Cr increased. 2013-07-17T02:17:18Z 2019-12-06T19:39:27Z 2013-07-17T02:17:18Z 2019-12-06T19:39:27Z 2012 2012 Journal Article Yin, K., Lo, I. M. C., Dong, H., Rao, P.,& Mak, M. S. H. (2012). Lab-scale simulation of the fate and transport of nano zero-valent iron in subsurface environments: Aggregation, sedimentation, and contaminant desorption. Journal of Hazardous Materials, 227-228, 118-125. 0304-3894 https://hdl.handle.net/10356/97154 http://hdl.handle.net/10220/11637 10.1016/j.jhazmat.2012.05.019 en Journal of hazardous materials © 2012 Elsevier B.V.
institution Nanyang Technological University
building NTU Library
country Singapore
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language English
description Heavy metal removal using nano zero-valent iron (NZVI) has drawn growing attention due to the ease of application and high removal efficiency. However, uncertainties regarding its fate and transport in subsurface environments have raised concerns that require further exploration. In this study, aggregation, sedimentation, and Cr/As desorption of three types of NZVIs were investigated under various conditions. It was found that the aggregation behavior of the NZVIs differed from one another in regard to reaction time and ionic strength, associated with the respective critical size for sedimentation. Sedimentation of NZVIs was positively related to the concentrations and average particle sizes. The sedimentation kinetics of NZVI followed two concomitant processes, i.e., (1) direct sedimentation of larger particles, and (2) initial aggregation and then sedimentation of smaller particles. When loaded with Cr/As, NZVIs tended to deposit faster, possibly due to the precipitation of Cr/As onto the nanoparticle surfaces resulting in larger particle sizes. Moreover, desorption of Cr/As from Cr/As loaded NZVIs was detected in the presence of typical groundwater ions, as well as natural organic matter, and poses a potential risk to the subsurface environment. The desorption of Cr was linearly related to the release of iron ions, while As desorption was mitigated when the immobilization of Cr increased.
author2 School of Civil and Environmental Engineering
author_facet School of Civil and Environmental Engineering
Lo, Irene M. C.
Mak, Mark S. H.
Yin, Ke
Dong, Haoran
Rao, Pinhua
format Article
author Lo, Irene M. C.
Mak, Mark S. H.
Yin, Ke
Dong, Haoran
Rao, Pinhua
spellingShingle Lo, Irene M. C.
Mak, Mark S. H.
Yin, Ke
Dong, Haoran
Rao, Pinhua
Lab-scale simulation of the fate and transport of nano zero-valent iron in subsurface environments : aggregation, sedimentation, and contaminant desorption
author_sort Lo, Irene M. C.
title Lab-scale simulation of the fate and transport of nano zero-valent iron in subsurface environments : aggregation, sedimentation, and contaminant desorption
title_short Lab-scale simulation of the fate and transport of nano zero-valent iron in subsurface environments : aggregation, sedimentation, and contaminant desorption
title_full Lab-scale simulation of the fate and transport of nano zero-valent iron in subsurface environments : aggregation, sedimentation, and contaminant desorption
title_fullStr Lab-scale simulation of the fate and transport of nano zero-valent iron in subsurface environments : aggregation, sedimentation, and contaminant desorption
title_full_unstemmed Lab-scale simulation of the fate and transport of nano zero-valent iron in subsurface environments : aggregation, sedimentation, and contaminant desorption
title_sort lab-scale simulation of the fate and transport of nano zero-valent iron in subsurface environments : aggregation, sedimentation, and contaminant desorption
publishDate 2013
url https://hdl.handle.net/10356/97154
http://hdl.handle.net/10220/11637
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