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Easily Regenerated Readily Deployable Absorbent for Heavy Metal Removal from Contaminated Water
Although clean and abundant water is the keystone of thriving communities, increasing demand and volatile climate patterns are depleting rivers and aquifers. Moreover, the quality of such water sources is threatened by noxious contaminants, of which heavy metals represents an area of growing concern...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5532212/ https://www.ncbi.nlm.nih.gov/pubmed/28751753 http://dx.doi.org/10.1038/s41598-017-06734-7 |
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author | Alagappan, Perry N. Heimann, Jessica Morrow, Lauren Andreoli, Enrico Barron, Andrew R. |
author_facet | Alagappan, Perry N. Heimann, Jessica Morrow, Lauren Andreoli, Enrico Barron, Andrew R. |
author_sort | Alagappan, Perry N. |
collection | PubMed |
description | Although clean and abundant water is the keystone of thriving communities, increasing demand and volatile climate patterns are depleting rivers and aquifers. Moreover, the quality of such water sources is threatened by noxious contaminants, of which heavy metals represents an area of growing concern. Recently, graphene oxide (GO) has been suggested as an adsorbent; however, a support is desirable to ensure a high surface area and an immobile phase. Herein, we described the preparation and characterization of a supported-epoxidized carbon nanotube (SENT) via the growth of multi walled carbon nanotubes (MWNTs) onto a quartz substrate. Subsequent epoxidation provides sufficient functionality to enable adsorbent of heavy metals (Cd(2+), Co(2+), Cu(2+), Hg(2+), Ni(2+), and Pb(2+)) from aqueous solution with initial concentrations (60–6000 ppm) chosen to simulate high industrial wastewater contamination. The SENT adsorption efficiency is >99.4% for all metals and the saturation concentration is significantly greater than observed for either GO or acid treated MWNTs. The SENT adsorbent may be readily regenerated under mild conditions using a globally available household chemical, vinegar. 1 g of SENT has the potential to treat 83,000 L of contaminated water down to WHO limits which would be sufficient for 11,000 people. |
format | Online Article Text |
id | pubmed-5532212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55322122017-08-02 Easily Regenerated Readily Deployable Absorbent for Heavy Metal Removal from Contaminated Water Alagappan, Perry N. Heimann, Jessica Morrow, Lauren Andreoli, Enrico Barron, Andrew R. Sci Rep Article Although clean and abundant water is the keystone of thriving communities, increasing demand and volatile climate patterns are depleting rivers and aquifers. Moreover, the quality of such water sources is threatened by noxious contaminants, of which heavy metals represents an area of growing concern. Recently, graphene oxide (GO) has been suggested as an adsorbent; however, a support is desirable to ensure a high surface area and an immobile phase. Herein, we described the preparation and characterization of a supported-epoxidized carbon nanotube (SENT) via the growth of multi walled carbon nanotubes (MWNTs) onto a quartz substrate. Subsequent epoxidation provides sufficient functionality to enable adsorbent of heavy metals (Cd(2+), Co(2+), Cu(2+), Hg(2+), Ni(2+), and Pb(2+)) from aqueous solution with initial concentrations (60–6000 ppm) chosen to simulate high industrial wastewater contamination. The SENT adsorption efficiency is >99.4% for all metals and the saturation concentration is significantly greater than observed for either GO or acid treated MWNTs. The SENT adsorbent may be readily regenerated under mild conditions using a globally available household chemical, vinegar. 1 g of SENT has the potential to treat 83,000 L of contaminated water down to WHO limits which would be sufficient for 11,000 people. Nature Publishing Group UK 2017-07-27 /pmc/articles/PMC5532212/ /pubmed/28751753 http://dx.doi.org/10.1038/s41598-017-06734-7 Text en © The Author(s) 2017 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 Alagappan, Perry N. Heimann, Jessica Morrow, Lauren Andreoli, Enrico Barron, Andrew R. Easily Regenerated Readily Deployable Absorbent for Heavy Metal Removal from Contaminated Water |
title | Easily Regenerated Readily Deployable Absorbent for Heavy Metal Removal from Contaminated Water |
title_full | Easily Regenerated Readily Deployable Absorbent for Heavy Metal Removal from Contaminated Water |
title_fullStr | Easily Regenerated Readily Deployable Absorbent for Heavy Metal Removal from Contaminated Water |
title_full_unstemmed | Easily Regenerated Readily Deployable Absorbent for Heavy Metal Removal from Contaminated Water |
title_short | Easily Regenerated Readily Deployable Absorbent for Heavy Metal Removal from Contaminated Water |
title_sort | easily regenerated readily deployable absorbent for heavy metal removal from contaminated water |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5532212/ https://www.ncbi.nlm.nih.gov/pubmed/28751753 http://dx.doi.org/10.1038/s41598-017-06734-7 |
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