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Accelerated phosphorus recovery from aqueous solution onto decorated sewage sludge carbon

In search of efficient phosphorus resource recovery and pollution remediation should be highly concerned due to the view of phosphorus nonrenewable and eutrophication. This work presented a new insight into conversion of sewage sludge into favorable carbonaceous adsorbent for accelerated removing an...

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Autores principales: Kong, Lingjun, Hu, Xingliang, Xie, Ziying, Ren, Xinyong, Long, Jianyou, Su, Minhua, Diao, Zenghui, Chen, Diyun, Shih, Kaimin, Hou, Li’an
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128935/
https://www.ncbi.nlm.nih.gov/pubmed/30194435
http://dx.doi.org/10.1038/s41598-018-31750-6
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author Kong, Lingjun
Hu, Xingliang
Xie, Ziying
Ren, Xinyong
Long, Jianyou
Su, Minhua
Diao, Zenghui
Chen, Diyun
Shih, Kaimin
Hou, Li’an
author_facet Kong, Lingjun
Hu, Xingliang
Xie, Ziying
Ren, Xinyong
Long, Jianyou
Su, Minhua
Diao, Zenghui
Chen, Diyun
Shih, Kaimin
Hou, Li’an
author_sort Kong, Lingjun
collection PubMed
description In search of efficient phosphorus resource recovery and pollution remediation should be highly concerned due to the view of phosphorus nonrenewable and eutrophication. This work presented a new insight into conversion of sewage sludge into favorable carbonaceous adsorbent for accelerated removing and recovering phosphorus from aqueous solution, what addressed the issues of phosphorus recovery and pollution remediation as well as sludge disposal. Ca and water hyacinth were evolved to decorate sludge derived carbon. Effect of mass ratio of sludge, water hyacinth and calcium carbonate on the morphologies and adsorption kinetics was investigated. The adsorbents (SW-Ca-112) resulted from sludge in the presence of water hyacinth and CaCO(3) in a mass ratio of 1:1:2 had the highest adsorption capacity of 49.50 mg/g P and adsorption rate. Decoration of Ca favored adsorption ability and the presence of water hyacinth accelerated the adsorption rate due to the enhanced porosity. Formation of acicular Ca(5)(PO(4))(3)OH nanoparticles contributed to the favorable adsorption process. Thus, the contribution of decorated Ca and water hyacinth to the adsorption ability and rate to phosphorus was understand, providing important information on resource utilization of sewage sludge as efficient adsorbent for immobilizing phosphorus from aqueous solution.
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spelling pubmed-61289352018-09-10 Accelerated phosphorus recovery from aqueous solution onto decorated sewage sludge carbon Kong, Lingjun Hu, Xingliang Xie, Ziying Ren, Xinyong Long, Jianyou Su, Minhua Diao, Zenghui Chen, Diyun Shih, Kaimin Hou, Li’an Sci Rep Article In search of efficient phosphorus resource recovery and pollution remediation should be highly concerned due to the view of phosphorus nonrenewable and eutrophication. This work presented a new insight into conversion of sewage sludge into favorable carbonaceous adsorbent for accelerated removing and recovering phosphorus from aqueous solution, what addressed the issues of phosphorus recovery and pollution remediation as well as sludge disposal. Ca and water hyacinth were evolved to decorate sludge derived carbon. Effect of mass ratio of sludge, water hyacinth and calcium carbonate on the morphologies and adsorption kinetics was investigated. The adsorbents (SW-Ca-112) resulted from sludge in the presence of water hyacinth and CaCO(3) in a mass ratio of 1:1:2 had the highest adsorption capacity of 49.50 mg/g P and adsorption rate. Decoration of Ca favored adsorption ability and the presence of water hyacinth accelerated the adsorption rate due to the enhanced porosity. Formation of acicular Ca(5)(PO(4))(3)OH nanoparticles contributed to the favorable adsorption process. Thus, the contribution of decorated Ca and water hyacinth to the adsorption ability and rate to phosphorus was understand, providing important information on resource utilization of sewage sludge as efficient adsorbent for immobilizing phosphorus from aqueous solution. Nature Publishing Group UK 2018-09-07 /pmc/articles/PMC6128935/ /pubmed/30194435 http://dx.doi.org/10.1038/s41598-018-31750-6 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kong, Lingjun
Hu, Xingliang
Xie, Ziying
Ren, Xinyong
Long, Jianyou
Su, Minhua
Diao, Zenghui
Chen, Diyun
Shih, Kaimin
Hou, Li’an
Accelerated phosphorus recovery from aqueous solution onto decorated sewage sludge carbon
title Accelerated phosphorus recovery from aqueous solution onto decorated sewage sludge carbon
title_full Accelerated phosphorus recovery from aqueous solution onto decorated sewage sludge carbon
title_fullStr Accelerated phosphorus recovery from aqueous solution onto decorated sewage sludge carbon
title_full_unstemmed Accelerated phosphorus recovery from aqueous solution onto decorated sewage sludge carbon
title_short Accelerated phosphorus recovery from aqueous solution onto decorated sewage sludge carbon
title_sort accelerated phosphorus recovery from aqueous solution onto decorated sewage sludge carbon
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128935/
https://www.ncbi.nlm.nih.gov/pubmed/30194435
http://dx.doi.org/10.1038/s41598-018-31750-6
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