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Surface Interactions between Gold Nanoparticles and Biochar
Engineered nanomaterials are directly applied to the agricultural soils as a part of pesticide/fertilize formulations or sludge/manure amendments. No prior reports are available to understand the surface interactions between gold nanoparticles (nAu) and soil components, including the charcoal black...
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/PMC5503990/ https://www.ncbi.nlm.nih.gov/pubmed/28694426 http://dx.doi.org/10.1038/s41598-017-03916-1 |
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author | Uchimiya, Minori Pignatello, Joseph J. White, Jason C. Hu, Szu-Lung Ferreira, Paulo J. |
author_facet | Uchimiya, Minori Pignatello, Joseph J. White, Jason C. Hu, Szu-Lung Ferreira, Paulo J. |
author_sort | Uchimiya, Minori |
collection | PubMed |
description | Engineered nanomaterials are directly applied to the agricultural soils as a part of pesticide/fertilize formulations or sludge/manure amendments. No prior reports are available to understand the surface interactions between gold nanoparticles (nAu) and soil components, including the charcoal black carbon (biochar). Retention of citrate-capped nAu on 300–700 °C pecan shell biochars occurred rapidly and irreversibly even at neutral pH where retention was less favorable. Uniform organic (primarily citrate ligands) layer on nAu was observable by TEM, and was preserved after the retention by biochar, which resulted in the aggregation or alignment along the edges of multisheets composing biochar. Retention of nAu was (i) greater on biochars than a sandy loam soil, (ii) greater at higher ionic strength and lower pH, and (iii) pyrolysis temperature-dependent: 500 < 700 ≪ 300 °C at pH 3. Collectively, carboxyl-enriched 300 °C biochar likely formed strong hydrogen bonds with the citrate layer of nAu. The charge transfer between the conduction band of nAu and π* continuum of polyaromatic sheets is likely to dominate on 700 °C biochar. Surface area-normalized retention of nAu on biochars was several orders of magnitude higher than negatively charged hydroxyl-bearing environmental surfaces, indicating the importance of black carbon in the environmental fate of engineered nanomaterials. |
format | Online Article Text |
id | pubmed-5503990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55039902017-07-12 Surface Interactions between Gold Nanoparticles and Biochar Uchimiya, Minori Pignatello, Joseph J. White, Jason C. Hu, Szu-Lung Ferreira, Paulo J. Sci Rep Article Engineered nanomaterials are directly applied to the agricultural soils as a part of pesticide/fertilize formulations or sludge/manure amendments. No prior reports are available to understand the surface interactions between gold nanoparticles (nAu) and soil components, including the charcoal black carbon (biochar). Retention of citrate-capped nAu on 300–700 °C pecan shell biochars occurred rapidly and irreversibly even at neutral pH where retention was less favorable. Uniform organic (primarily citrate ligands) layer on nAu was observable by TEM, and was preserved after the retention by biochar, which resulted in the aggregation or alignment along the edges of multisheets composing biochar. Retention of nAu was (i) greater on biochars than a sandy loam soil, (ii) greater at higher ionic strength and lower pH, and (iii) pyrolysis temperature-dependent: 500 < 700 ≪ 300 °C at pH 3. Collectively, carboxyl-enriched 300 °C biochar likely formed strong hydrogen bonds with the citrate layer of nAu. The charge transfer between the conduction band of nAu and π* continuum of polyaromatic sheets is likely to dominate on 700 °C biochar. Surface area-normalized retention of nAu on biochars was several orders of magnitude higher than negatively charged hydroxyl-bearing environmental surfaces, indicating the importance of black carbon in the environmental fate of engineered nanomaterials. Nature Publishing Group UK 2017-07-10 /pmc/articles/PMC5503990/ /pubmed/28694426 http://dx.doi.org/10.1038/s41598-017-03916-1 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 Uchimiya, Minori Pignatello, Joseph J. White, Jason C. Hu, Szu-Lung Ferreira, Paulo J. Surface Interactions between Gold Nanoparticles and Biochar |
title | Surface Interactions between Gold Nanoparticles and Biochar |
title_full | Surface Interactions between Gold Nanoparticles and Biochar |
title_fullStr | Surface Interactions between Gold Nanoparticles and Biochar |
title_full_unstemmed | Surface Interactions between Gold Nanoparticles and Biochar |
title_short | Surface Interactions between Gold Nanoparticles and Biochar |
title_sort | surface interactions between gold nanoparticles and biochar |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5503990/ https://www.ncbi.nlm.nih.gov/pubmed/28694426 http://dx.doi.org/10.1038/s41598-017-03916-1 |
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