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Phosphorous extraction and heavy metal separation from sewage sludge ash by two-compartment electrodialysis in an upscaled tube reactor

Two-compartment electrodialytic extraction (2C-ED) is a one-step process for the simultaneous phosphorous extraction and separation of heavy metals from sewage sludge ash (SSA). The process is driven by an applied electric DC field, which can be supplied from renewable sources. The proof-of-concept...

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Autores principales: Ottosen, Lisbeth M., Thornberg, Dines
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10682058/
https://www.ncbi.nlm.nih.gov/pubmed/37872344
http://dx.doi.org/10.1007/s11356-023-30384-0
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author Ottosen, Lisbeth M.
Thornberg, Dines
author_facet Ottosen, Lisbeth M.
Thornberg, Dines
author_sort Ottosen, Lisbeth M.
collection PubMed
description Two-compartment electrodialytic extraction (2C-ED) is a one-step process for the simultaneous phosphorous extraction and separation of heavy metals from sewage sludge ash (SSA). The process is driven by an applied electric DC field, which can be supplied from renewable sources. The proof-of-concept of the method was conducted in small laboratory cells; however, upscaling to a continuous 2C-ED process, which additionally can treat SSA suspensions at a low liquid-to-solid (L:S) ratio, requires a new design. This paper presents such a new design. In principle, ED consists of two compartments separated by a cation exchange membrane. One compartment contains a suspension of SSA in water and the anode. A cathode is placed in the other compartment. Electrolysis at the anode acidifies the suspension causing the dissolution of phosphorous and heavy metals. The heavy metals are separated from the suspension by electromigration into the catholyte, whereas the dissolved phosphorous remains in the dispersion solution. In the new design, the SSA was suspended in a tube-shaped reactor with the cation exchange membrane covering the outside. The reactor was placed in a container with the catholyte. Periodically turning off the reactor kept SSA in suspension even at a low L:S ratio without corners and pockets where the SSA otherwise tends to settle. Five 2C-ED experiments were conducted with 1.5 to 3 kg SSA at varying currents and durations. Up to 89% P was extracted. The extracted P was concentrated in the dispersion solution of the SSA suspension, where the obtained P-related concentrations of heavy metals were far below the limiting values for spreading on agricultural land. The experiments underlined that treating the SSA in a suspension with a low L:S ratio is advantageous. A comparison to previous laboratory experiments in small cells treating 50 g SSA shows a significantly more efficient use of the applied current in the new reactor setup. Thus, the new reactor design for 2C-ED fulfilled the set criteria for the operation and did additionally result in a higher efficiency than the laboratory setups, i.e., the design can be the first step towards an upscaling.
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spelling pubmed-106820582023-11-30 Phosphorous extraction and heavy metal separation from sewage sludge ash by two-compartment electrodialysis in an upscaled tube reactor Ottosen, Lisbeth M. Thornberg, Dines Environ Sci Pollut Res Int Research Article Two-compartment electrodialytic extraction (2C-ED) is a one-step process for the simultaneous phosphorous extraction and separation of heavy metals from sewage sludge ash (SSA). The process is driven by an applied electric DC field, which can be supplied from renewable sources. The proof-of-concept of the method was conducted in small laboratory cells; however, upscaling to a continuous 2C-ED process, which additionally can treat SSA suspensions at a low liquid-to-solid (L:S) ratio, requires a new design. This paper presents such a new design. In principle, ED consists of two compartments separated by a cation exchange membrane. One compartment contains a suspension of SSA in water and the anode. A cathode is placed in the other compartment. Electrolysis at the anode acidifies the suspension causing the dissolution of phosphorous and heavy metals. The heavy metals are separated from the suspension by electromigration into the catholyte, whereas the dissolved phosphorous remains in the dispersion solution. In the new design, the SSA was suspended in a tube-shaped reactor with the cation exchange membrane covering the outside. The reactor was placed in a container with the catholyte. Periodically turning off the reactor kept SSA in suspension even at a low L:S ratio without corners and pockets where the SSA otherwise tends to settle. Five 2C-ED experiments were conducted with 1.5 to 3 kg SSA at varying currents and durations. Up to 89% P was extracted. The extracted P was concentrated in the dispersion solution of the SSA suspension, where the obtained P-related concentrations of heavy metals were far below the limiting values for spreading on agricultural land. The experiments underlined that treating the SSA in a suspension with a low L:S ratio is advantageous. A comparison to previous laboratory experiments in small cells treating 50 g SSA shows a significantly more efficient use of the applied current in the new reactor setup. Thus, the new reactor design for 2C-ED fulfilled the set criteria for the operation and did additionally result in a higher efficiency than the laboratory setups, i.e., the design can be the first step towards an upscaling. Springer Berlin Heidelberg 2023-10-24 2023 /pmc/articles/PMC10682058/ /pubmed/37872344 http://dx.doi.org/10.1007/s11356-023-30384-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Ottosen, Lisbeth M.
Thornberg, Dines
Phosphorous extraction and heavy metal separation from sewage sludge ash by two-compartment electrodialysis in an upscaled tube reactor
title Phosphorous extraction and heavy metal separation from sewage sludge ash by two-compartment electrodialysis in an upscaled tube reactor
title_full Phosphorous extraction and heavy metal separation from sewage sludge ash by two-compartment electrodialysis in an upscaled tube reactor
title_fullStr Phosphorous extraction and heavy metal separation from sewage sludge ash by two-compartment electrodialysis in an upscaled tube reactor
title_full_unstemmed Phosphorous extraction and heavy metal separation from sewage sludge ash by two-compartment electrodialysis in an upscaled tube reactor
title_short Phosphorous extraction and heavy metal separation from sewage sludge ash by two-compartment electrodialysis in an upscaled tube reactor
title_sort phosphorous extraction and heavy metal separation from sewage sludge ash by two-compartment electrodialysis in an upscaled tube reactor
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10682058/
https://www.ncbi.nlm.nih.gov/pubmed/37872344
http://dx.doi.org/10.1007/s11356-023-30384-0
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