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Electrochemical Induced Calcium Phosphate Precipitation: Importance of Local pH
[Image: see text] Phosphorus (P) is an essential nutrient for living organisms and cannot be replaced or substituted. In this paper, we present a simple yet efficient membrane free electrochemical system for P removal and recovery as calcium phosphate (CaP). This method relies on in situ formation o...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5628374/ https://www.ncbi.nlm.nih.gov/pubmed/28872838 http://dx.doi.org/10.1021/acs.est.7b03909 |
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author | Lei, Yang Song, Bingnan van der Weijden, Renata D. Saakes, Michel Buisman, Cees J. N. |
author_facet | Lei, Yang Song, Bingnan van der Weijden, Renata D. Saakes, Michel Buisman, Cees J. N. |
author_sort | Lei, Yang |
collection | PubMed |
description | [Image: see text] Phosphorus (P) is an essential nutrient for living organisms and cannot be replaced or substituted. In this paper, we present a simple yet efficient membrane free electrochemical system for P removal and recovery as calcium phosphate (CaP). This method relies on in situ formation of hydroxide ions by electro mediated water reduction at a titanium cathode surface. The in situ raised pH at the cathode provides a local environment where CaP will become highly supersaturated. Therefore, homogeneous and heterogeneous nucleation of CaP occurs near and at the cathode surface. Because of the local high pH, the P removal behavior is not sensitive to bulk solution pH and therefore, efficient P removal was observed in three studied bulk solutions with pH of 4.0 (56.1%), 8.2 (57.4%), and 10.0 (48.4%) after 24 h of reaction time. While P removal efficiencies are not generally affected by bulk solution pH, the chemical-physical properties of CaP solids collected on the cathode are still related to bulk solution pH, as confirmed by structure characterizations. High initial solution pH promotes the formation of more crystalline products with relatively high Ca/P molar ratio. The Ca/P molar ratio increases from 1.30 (pH 4.0) to 1.38 (pH 8.2) and further increases to 1.55 (pH 10.0). The formation of CaP precipitates was a typical crystallization process, with an amorphous phase formed at the initial stage which then transforms to the most stable crystal phase, hydroxyapatite, which is inferred from the increased Ca/P molar ratio from 1.38 (day 1) to the theoretical 1.76 (day 11) and by the formation of needle-like crystals. Finally, we demonstrated the efficiency of this system for real wastewater. This, together with the fact that the electrochemical method can work at low bulk pH, without dosing chemicals and a need for a separation process, highlights the potential application of the electrochemical method for P removal and recovery. |
format | Online Article Text |
id | pubmed-5628374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-56283742017-10-06 Electrochemical Induced Calcium Phosphate Precipitation: Importance of Local pH Lei, Yang Song, Bingnan van der Weijden, Renata D. Saakes, Michel Buisman, Cees J. N. Environ Sci Technol [Image: see text] Phosphorus (P) is an essential nutrient for living organisms and cannot be replaced or substituted. In this paper, we present a simple yet efficient membrane free electrochemical system for P removal and recovery as calcium phosphate (CaP). This method relies on in situ formation of hydroxide ions by electro mediated water reduction at a titanium cathode surface. The in situ raised pH at the cathode provides a local environment where CaP will become highly supersaturated. Therefore, homogeneous and heterogeneous nucleation of CaP occurs near and at the cathode surface. Because of the local high pH, the P removal behavior is not sensitive to bulk solution pH and therefore, efficient P removal was observed in three studied bulk solutions with pH of 4.0 (56.1%), 8.2 (57.4%), and 10.0 (48.4%) after 24 h of reaction time. While P removal efficiencies are not generally affected by bulk solution pH, the chemical-physical properties of CaP solids collected on the cathode are still related to bulk solution pH, as confirmed by structure characterizations. High initial solution pH promotes the formation of more crystalline products with relatively high Ca/P molar ratio. The Ca/P molar ratio increases from 1.30 (pH 4.0) to 1.38 (pH 8.2) and further increases to 1.55 (pH 10.0). The formation of CaP precipitates was a typical crystallization process, with an amorphous phase formed at the initial stage which then transforms to the most stable crystal phase, hydroxyapatite, which is inferred from the increased Ca/P molar ratio from 1.38 (day 1) to the theoretical 1.76 (day 11) and by the formation of needle-like crystals. Finally, we demonstrated the efficiency of this system for real wastewater. This, together with the fact that the electrochemical method can work at low bulk pH, without dosing chemicals and a need for a separation process, highlights the potential application of the electrochemical method for P removal and recovery. American Chemical Society 2017-09-05 2017-10-03 /pmc/articles/PMC5628374/ /pubmed/28872838 http://dx.doi.org/10.1021/acs.est.7b03909 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Lei, Yang Song, Bingnan van der Weijden, Renata D. Saakes, Michel Buisman, Cees J. N. Electrochemical Induced Calcium Phosphate Precipitation: Importance of Local pH |
title | Electrochemical
Induced Calcium Phosphate Precipitation:
Importance of Local pH |
title_full | Electrochemical
Induced Calcium Phosphate Precipitation:
Importance of Local pH |
title_fullStr | Electrochemical
Induced Calcium Phosphate Precipitation:
Importance of Local pH |
title_full_unstemmed | Electrochemical
Induced Calcium Phosphate Precipitation:
Importance of Local pH |
title_short | Electrochemical
Induced Calcium Phosphate Precipitation:
Importance of Local pH |
title_sort | electrochemical
induced calcium phosphate precipitation:
importance of local ph |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5628374/ https://www.ncbi.nlm.nih.gov/pubmed/28872838 http://dx.doi.org/10.1021/acs.est.7b03909 |
work_keys_str_mv | AT leiyang electrochemicalinducedcalciumphosphateprecipitationimportanceoflocalph AT songbingnan electrochemicalinducedcalciumphosphateprecipitationimportanceoflocalph AT vanderweijdenrenatad electrochemicalinducedcalciumphosphateprecipitationimportanceoflocalph AT saakesmichel electrochemicalinducedcalciumphosphateprecipitationimportanceoflocalph AT buismanceesjn electrochemicalinducedcalciumphosphateprecipitationimportanceoflocalph |