Screening redox stability of iron rich by-products for effective phosphate immobilisation in freshwater sediments

Iron (Fe) rich by-products can be added to lake or river sediments to immobilise phosphate (PO4) and lower eutrophication risks. These Fe materials differ in mineralogy and specific surface area, hence differing in PO4 sorption capacity and stability under reducing conditions. This study was set up...

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Veröffentlicht in:Journal of environmental management 2023-07, Vol.337, p.117728-117728, Article 117728
Hauptverfasser: Xia, Lei, Vangansbeke, Arne, Lauryssen, Florian, Smolders, Erik
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Vangansbeke, Arne
Lauryssen, Florian
Smolders, Erik
description Iron (Fe) rich by-products can be added to lake or river sediments to immobilise phosphate (PO4) and lower eutrophication risks. These Fe materials differ in mineralogy and specific surface area, hence differing in PO4 sorption capacity and stability under reducing conditions. This study was set up to identify key properties of these amendments in their capacity to immobilise PO4 in sediments. Eleven Fe rich by-products, collected from drinking water treatment plants and acid mine drainage, were characterised. The PO4 adsorption to these by-products was first determined under aerobic conditions and the solid-liquid distribution coefficient KD for PO4 correlated strongly to oxalate extractable Fe content. A static sediment-water incubation test was subsequently used to evaluate the redox stability of these by-products. The reductive processes gradually released Fe to solution and more Fe was release from the amended than from the control sediments. The total Fe release to solution was positively related to ascorbate reducible Fe fractions in the by-products, suggesting that such fractions indicate potential loss of P retention capacity on the long term. The final PO4 concentration in the overlying water was 5.6 mg P L−1 in the control and was successfully lowered by factor 30–420 depending on the by-product. The factor by which solution PO4 was reduced in Fe treatments increased with increasing KD determined under aerobic conditions. This study suggests that efficient by-products to trap P in sediments are characterised by a high oxalate Fe content and a low reducible Fe fraction. •AsCorbate extractable Fe used as indicator for Fe stability of Fe rich by-products.•The distribution coefficient KD positively correlated to oxalate extractable Fe.•The P reduction by Fe rich by-product under anoxia increases with increasing KD.•The P reduction by Fe rich by-product decreases with increased molar P/Fe ratio.
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The total Fe release to solution was positively related to ascorbate reducible Fe fractions in the by-products, suggesting that such fractions indicate potential loss of P retention capacity on the long term. The final PO4 concentration in the overlying water was 5.6 mg P L−1 in the control and was successfully lowered by factor 30–420 depending on the by-product. The factor by which solution PO4 was reduced in Fe treatments increased with increasing KD determined under aerobic conditions. This study suggests that efficient by-products to trap P in sediments are characterised by a high oxalate Fe content and a low reducible Fe fraction. •AsCorbate extractable Fe used as indicator for Fe stability of Fe rich by-products.•The distribution coefficient KD positively correlated to oxalate extractable Fe.•The P reduction by Fe rich by-product under anoxia increases with increasing KD.•The P reduction by Fe rich by-product decreases with increased molar P/Fe ratio.</description><identifier>ISSN: 0301-4797</identifier><identifier>EISSN: 1095-8630</identifier><identifier>DOI: 10.1016/j.jenvman.2023.117728</identifier><identifier>PMID: 36940601</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Geologic Sediments ; Iron - analysis ; Iron oxides extraction ; Iron rich by-products ; Iron stability ; Lakes ; Oxidation-Reduction ; Phosphate immobilisation ; Phosphates ; Phosphorus ; Water Pollutants, Chemical - analysis</subject><ispartof>Journal of environmental management, 2023-07, Vol.337, p.117728-117728, Article 117728</ispartof><rights>2023</rights><rights>Copyright © 2023. 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These Fe materials differ in mineralogy and specific surface area, hence differing in PO4 sorption capacity and stability under reducing conditions. This study was set up to identify key properties of these amendments in their capacity to immobilise PO4 in sediments. Eleven Fe rich by-products, collected from drinking water treatment plants and acid mine drainage, were characterised. The PO4 adsorption to these by-products was first determined under aerobic conditions and the solid-liquid distribution coefficient KD for PO4 correlated strongly to oxalate extractable Fe content. A static sediment-water incubation test was subsequently used to evaluate the redox stability of these by-products. The reductive processes gradually released Fe to solution and more Fe was release from the amended than from the control sediments. The total Fe release to solution was positively related to ascorbate reducible Fe fractions in the by-products, suggesting that such fractions indicate potential loss of P retention capacity on the long term. The final PO4 concentration in the overlying water was 5.6 mg P L−1 in the control and was successfully lowered by factor 30–420 depending on the by-product. The factor by which solution PO4 was reduced in Fe treatments increased with increasing KD determined under aerobic conditions. 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The total Fe release to solution was positively related to ascorbate reducible Fe fractions in the by-products, suggesting that such fractions indicate potential loss of P retention capacity on the long term. The final PO4 concentration in the overlying water was 5.6 mg P L−1 in the control and was successfully lowered by factor 30–420 depending on the by-product. The factor by which solution PO4 was reduced in Fe treatments increased with increasing KD determined under aerobic conditions. This study suggests that efficient by-products to trap P in sediments are characterised by a high oxalate Fe content and a low reducible Fe fraction. •AsCorbate extractable Fe used as indicator for Fe stability of Fe rich by-products.•The distribution coefficient KD positively correlated to oxalate extractable Fe.•The P reduction by Fe rich by-product under anoxia increases with increasing KD.•The P reduction by Fe rich by-product decreases with increased molar P/Fe ratio.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>36940601</pmid><doi>10.1016/j.jenvman.2023.117728</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-2277-2135</orcidid><orcidid>https://orcid.org/0000-0002-5941-8810</orcidid><orcidid>https://orcid.org/0000-0002-9701-5078</orcidid><orcidid>https://orcid.org/0000-0003-3054-2444</orcidid></addata></record>
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subjects Geologic Sediments
Iron - analysis
Iron oxides extraction
Iron rich by-products
Iron stability
Lakes
Oxidation-Reduction
Phosphate immobilisation
Phosphates
Phosphorus
Water Pollutants, Chemical - analysis
title Screening redox stability of iron rich by-products for effective phosphate immobilisation in freshwater sediments
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