Co-transport of U(VI) and akaganéite colloids in water-saturated porous media: Role of U(VI) concentration, pH and ionic strength

Remediating uranium contamination becomes a worldwide interest because of increasing uranium release from mining activities. Due to ubiquitous presence of pyrite and the application of iron-based technology, colloidal iron oxy-hydroxides such as akaganéite colloid (AKC) extensively exist in uranium...

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Veröffentlicht in:Water research (Oxford) 2018-12, Vol.147, p.350-361
Hauptverfasser: Ge, Mengtuan, Wang, Dengjun, Yang, Junwei, Jin, Qiang, Chen, Zongyuan, Wu, Wangsuo, Guo, Zhijun
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container_start_page 350
container_title Water research (Oxford)
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creator Ge, Mengtuan
Wang, Dengjun
Yang, Junwei
Jin, Qiang
Chen, Zongyuan
Wu, Wangsuo
Guo, Zhijun
description Remediating uranium contamination becomes a worldwide interest because of increasing uranium release from mining activities. Due to ubiquitous presence of pyrite and the application of iron-based technology, colloidal iron oxy-hydroxides such as akaganéite colloid (AKC) extensively exist in uranium polluted water at uranium tailing sites. In this context, we studied individual and co-transport of U(VI) and AKC in water-saturated sand columns at 50 mg/L AKC and environmentally relevant U(VI) concentrations (5.0 × 10−7 ∼ 5.0 × 10−5 M). It was found that, in addition to the impact of pH and ionic strength, whether AKC facilitated U(VI) transport depended on U(VI) concentration as well. The presence of AKC facilitated U(VI) transport at relatively low U(VI) concentration (5.0 × 10−7 ∼ 5.0 × 10−6 M), which was due to the strong adsorption of U(VI) on AKC and faster transport of AKC than that U(VI) as observed in their individual transport experiments. At relatively high U(VI) concentrations (5.0 × 10−5 M), however, AKC impeded U(VI) transport because U(VI) of high concentration decreased AKC colloidal stability and increased AKC aggregation and attachment. Thus, U(VI) and AKC co-transport was even blocked completely at relatively high pH and ionic strength. The mechanisms behind the co-transport of U(VI) and AKC were also confirmed by assessing the evolutions of aqueous pH and AKC zeta potential and particle size distribution in the column effluents. A two-site non-equilibrium model and a two-site kinetic attachment/detachment model well-described the breakthrough curves of U(VI) and AKC, respectively. Knowledge generated from this study provides a thorough understanding of uranium transport in the absence/presence of AKC, and brings new insights into the influence of contaminant concentration on co-transport in the presence of colloids. [Display omitted] •Akaganéite colloids inhibit U(VI) transport at relatively high U(VI) concentration.•U(VI) concentration is a vital factor in regulating its co-transport with AKC.•U(VI) adsorption increases AKC size and impedes AKC transport.
doi_str_mv 10.1016/j.watres.2018.10.004
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Due to ubiquitous presence of pyrite and the application of iron-based technology, colloidal iron oxy-hydroxides such as akaganéite colloid (AKC) extensively exist in uranium polluted water at uranium tailing sites. In this context, we studied individual and co-transport of U(VI) and AKC in water-saturated sand columns at 50 mg/L AKC and environmentally relevant U(VI) concentrations (5.0 × 10−7 ∼ 5.0 × 10−5 M). It was found that, in addition to the impact of pH and ionic strength, whether AKC facilitated U(VI) transport depended on U(VI) concentration as well. The presence of AKC facilitated U(VI) transport at relatively low U(VI) concentration (5.0 × 10−7 ∼ 5.0 × 10−6 M), which was due to the strong adsorption of U(VI) on AKC and faster transport of AKC than that U(VI) as observed in their individual transport experiments. At relatively high U(VI) concentrations (5.0 × 10−5 M), however, AKC impeded U(VI) transport because U(VI) of high concentration decreased AKC colloidal stability and increased AKC aggregation and attachment. Thus, U(VI) and AKC co-transport was even blocked completely at relatively high pH and ionic strength. The mechanisms behind the co-transport of U(VI) and AKC were also confirmed by assessing the evolutions of aqueous pH and AKC zeta potential and particle size distribution in the column effluents. A two-site non-equilibrium model and a two-site kinetic attachment/detachment model well-described the breakthrough curves of U(VI) and AKC, respectively. Knowledge generated from this study provides a thorough understanding of uranium transport in the absence/presence of AKC, and brings new insights into the influence of contaminant concentration on co-transport in the presence of colloids. [Display omitted] •Akaganéite colloids inhibit U(VI) transport at relatively high U(VI) concentration.•U(VI) concentration is a vital factor in regulating its co-transport with AKC.•U(VI) adsorption increases AKC size and impedes AKC transport.</description><identifier>ISSN: 0043-1354</identifier><identifier>EISSN: 1879-2448</identifier><identifier>DOI: 10.1016/j.watres.2018.10.004</identifier><identifier>PMID: 30321825</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Akaganéite colloid ; Co-transport ; Concentration effect ; Modelling ; U(VI)</subject><ispartof>Water research (Oxford), 2018-12, Vol.147, p.350-361</ispartof><rights>2018 Elsevier Ltd</rights><rights>Copyright © 2018 Elsevier Ltd. 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Due to ubiquitous presence of pyrite and the application of iron-based technology, colloidal iron oxy-hydroxides such as akaganéite colloid (AKC) extensively exist in uranium polluted water at uranium tailing sites. In this context, we studied individual and co-transport of U(VI) and AKC in water-saturated sand columns at 50 mg/L AKC and environmentally relevant U(VI) concentrations (5.0 × 10−7 ∼ 5.0 × 10−5 M). It was found that, in addition to the impact of pH and ionic strength, whether AKC facilitated U(VI) transport depended on U(VI) concentration as well. The presence of AKC facilitated U(VI) transport at relatively low U(VI) concentration (5.0 × 10−7 ∼ 5.0 × 10−6 M), which was due to the strong adsorption of U(VI) on AKC and faster transport of AKC than that U(VI) as observed in their individual transport experiments. At relatively high U(VI) concentrations (5.0 × 10−5 M), however, AKC impeded U(VI) transport because U(VI) of high concentration decreased AKC colloidal stability and increased AKC aggregation and attachment. Thus, U(VI) and AKC co-transport was even blocked completely at relatively high pH and ionic strength. The mechanisms behind the co-transport of U(VI) and AKC were also confirmed by assessing the evolutions of aqueous pH and AKC zeta potential and particle size distribution in the column effluents. A two-site non-equilibrium model and a two-site kinetic attachment/detachment model well-described the breakthrough curves of U(VI) and AKC, respectively. Knowledge generated from this study provides a thorough understanding of uranium transport in the absence/presence of AKC, and brings new insights into the influence of contaminant concentration on co-transport in the presence of colloids. [Display omitted] •Akaganéite colloids inhibit U(VI) transport at relatively high U(VI) concentration.•U(VI) concentration is a vital factor in regulating its co-transport with AKC.•U(VI) adsorption increases AKC size and impedes AKC transport.</description><subject>Akaganéite colloid</subject><subject>Co-transport</subject><subject>Concentration effect</subject><subject>Modelling</subject><subject>U(VI)</subject><issn>0043-1354</issn><issn>1879-2448</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kM1OGzEUhS1UBCHtGyDkJZWY1H8z8XSBVEWFIEVCqkq3lmPfAYeJHWwH1C1v0-foi-GQQHdd-ero3HN8P4SOKRlRQpsvi9GTzhHSiBEqizQiROyhAZXjtmJCyA9oUBReUV6LQ3SU0oIQwhhvD9AhJ5xRyeoBep6EKkft0yrEjEOHb05_XX3G2lus7_Wt9n__uAzYhL4PzibsPC61EKuk8zqWyeKyGdYJL8E6_RX_CD38yzHBG_ClILvgz_Bq-ppcZmdwKr_3t_nuI9rvdJ_g0-4dopuL7z8n02p2fXk1-TarjGAyV1ZqTi0DbVknGlZzK4E1otbG1IIwKedadzVprKhtMyembanpbNM2nFIp5pIP0ek2dxXDwxpSVkuXDPS99lAOUIwyMq4JKXCGSGytJoaUInRqFd1Sx9-KErWhrxZqS19t6G_UDeshOtk1rOcFx_vSG-5iON8aoNz56CCqZBwURNZFMFnZ4P7f8AI-H5ir</recordid><startdate>20181215</startdate><enddate>20181215</enddate><creator>Ge, Mengtuan</creator><creator>Wang, Dengjun</creator><creator>Yang, Junwei</creator><creator>Jin, Qiang</creator><creator>Chen, Zongyuan</creator><creator>Wu, Wangsuo</creator><creator>Guo, Zhijun</creator><general>Elsevier Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20181215</creationdate><title>Co-transport of U(VI) and akaganéite colloids in water-saturated porous media: Role of U(VI) concentration, pH and ionic strength</title><author>Ge, Mengtuan ; Wang, Dengjun ; Yang, Junwei ; Jin, Qiang ; Chen, Zongyuan ; Wu, Wangsuo ; Guo, Zhijun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-d8a31d2ead2f46253d8e2645acc540288baaf506d45d6b0c991cfd69631184b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Akaganéite colloid</topic><topic>Co-transport</topic><topic>Concentration effect</topic><topic>Modelling</topic><topic>U(VI)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ge, Mengtuan</creatorcontrib><creatorcontrib>Wang, Dengjun</creatorcontrib><creatorcontrib>Yang, Junwei</creatorcontrib><creatorcontrib>Jin, Qiang</creatorcontrib><creatorcontrib>Chen, Zongyuan</creatorcontrib><creatorcontrib>Wu, Wangsuo</creatorcontrib><creatorcontrib>Guo, Zhijun</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Water research (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ge, Mengtuan</au><au>Wang, Dengjun</au><au>Yang, Junwei</au><au>Jin, Qiang</au><au>Chen, Zongyuan</au><au>Wu, Wangsuo</au><au>Guo, Zhijun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Co-transport of U(VI) and akaganéite colloids in water-saturated porous media: Role of U(VI) concentration, pH and ionic strength</atitle><jtitle>Water research (Oxford)</jtitle><addtitle>Water Res</addtitle><date>2018-12-15</date><risdate>2018</risdate><volume>147</volume><spage>350</spage><epage>361</epage><pages>350-361</pages><issn>0043-1354</issn><eissn>1879-2448</eissn><abstract>Remediating uranium contamination becomes a worldwide interest because of increasing uranium release from mining activities. Due to ubiquitous presence of pyrite and the application of iron-based technology, colloidal iron oxy-hydroxides such as akaganéite colloid (AKC) extensively exist in uranium polluted water at uranium tailing sites. In this context, we studied individual and co-transport of U(VI) and AKC in water-saturated sand columns at 50 mg/L AKC and environmentally relevant U(VI) concentrations (5.0 × 10−7 ∼ 5.0 × 10−5 M). It was found that, in addition to the impact of pH and ionic strength, whether AKC facilitated U(VI) transport depended on U(VI) concentration as well. The presence of AKC facilitated U(VI) transport at relatively low U(VI) concentration (5.0 × 10−7 ∼ 5.0 × 10−6 M), which was due to the strong adsorption of U(VI) on AKC and faster transport of AKC than that U(VI) as observed in their individual transport experiments. At relatively high U(VI) concentrations (5.0 × 10−5 M), however, AKC impeded U(VI) transport because U(VI) of high concentration decreased AKC colloidal stability and increased AKC aggregation and attachment. Thus, U(VI) and AKC co-transport was even blocked completely at relatively high pH and ionic strength. The mechanisms behind the co-transport of U(VI) and AKC were also confirmed by assessing the evolutions of aqueous pH and AKC zeta potential and particle size distribution in the column effluents. A two-site non-equilibrium model and a two-site kinetic attachment/detachment model well-described the breakthrough curves of U(VI) and AKC, respectively. Knowledge generated from this study provides a thorough understanding of uranium transport in the absence/presence of AKC, and brings new insights into the influence of contaminant concentration on co-transport in the presence of colloids. [Display omitted] •Akaganéite colloids inhibit U(VI) transport at relatively high U(VI) concentration.•U(VI) concentration is a vital factor in regulating its co-transport with AKC.•U(VI) adsorption increases AKC size and impedes AKC transport.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>30321825</pmid><doi>10.1016/j.watres.2018.10.004</doi><tpages>12</tpages></addata></record>
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subjects Akaganéite colloid
Co-transport
Concentration effect
Modelling
U(VI)
title Co-transport of U(VI) and akaganéite colloids in water-saturated porous media: Role of U(VI) concentration, pH and ionic strength
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