Sensitivity of the Transport of Plastic Nanoparticles to Typical Phosphates Associated with Ionic Strength and Solution pH
The influence of phosphates on the transport of plastic particles in porous media is environmentally relevant due to their ubiquitous coexistence in the subsurface environment. This study investigated the transport of plastic nanoparticles (PNPs) via column experiments, paired with Derjaguin–Landau–...
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MDPI AG
2022-08-01
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author | Xingyu Liu Yan Liang Yongtao Peng Tingting Meng Liling Xu Pengcheng Dong |
author_facet | Xingyu Liu Yan Liang Yongtao Peng Tingting Meng Liling Xu Pengcheng Dong |
author_sort | Xingyu Liu |
collection | DOAJ |
description | The influence of phosphates on the transport of plastic particles in porous media is environmentally relevant due to their ubiquitous coexistence in the subsurface environment. This study investigated the transport of plastic nanoparticles (PNPs) via column experiments, paired with Derjaguin–Landau–Verwey–Overbeek calculations and numerical simulations. The trends of PNP transport vary with increasing concentrations of NaH<sub>2</sub>PO<sub>4</sub> and Na<sub>2</sub>HPO<sub>4</sub> due to the coupled effects of increased electrostatic repulsion, the competition for retention sites, and the compression of the double layer. Higher pH tends to increase PNP transport due to the enhanced deprotonation of surfaces. The release of retained PNPs under reduced IS and increased pH is limited because most of the PNPs were irreversibly captured in deep primary minima. The presence of physicochemical heterogeneities on solid surfaces can reduce PNP transport and increase the sensitivity of the transport to IS. Furthermore, variations in the hydrogen bonding when the two phosphates act as proton donors will result in different influences on PNP transport at the same IS. This study highlights the sensitivity of PNP transport to phosphates associated with the solution chemistries (e.g., IS and pH) and is helpful for better understanding the fate of PNPs and other colloidal contaminants in the subsurface environment. |
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issn | 1661-6596 1422-0067 |
language | English |
last_indexed | 2024-03-10T01:44:01Z |
publishDate | 2022-08-01 |
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series | International Journal of Molecular Sciences |
spelling | doaj.art-2a9d67ecfc3f4fd2838a0c351aef24b82023-11-23T13:18:24ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672022-08-012317986010.3390/ijms23179860Sensitivity of the Transport of Plastic Nanoparticles to Typical Phosphates Associated with Ionic Strength and Solution pHXingyu Liu0Yan Liang1Yongtao Peng2Tingting Meng3Liling Xu4Pengcheng Dong5School of Resources, Environment and Materials, Guangxi University, Nanning 530004, ChinaSchool of Resources, Environment and Materials, Guangxi University, Nanning 530004, ChinaSchool of Resources, Environment and Materials, Guangxi University, Nanning 530004, ChinaSchool of Resources, Environment and Materials, Guangxi University, Nanning 530004, ChinaSchool of Resources, Environment and Materials, Guangxi University, Nanning 530004, ChinaSchool of Resources, Environment and Materials, Guangxi University, Nanning 530004, ChinaThe influence of phosphates on the transport of plastic particles in porous media is environmentally relevant due to their ubiquitous coexistence in the subsurface environment. This study investigated the transport of plastic nanoparticles (PNPs) via column experiments, paired with Derjaguin–Landau–Verwey–Overbeek calculations and numerical simulations. The trends of PNP transport vary with increasing concentrations of NaH<sub>2</sub>PO<sub>4</sub> and Na<sub>2</sub>HPO<sub>4</sub> due to the coupled effects of increased electrostatic repulsion, the competition for retention sites, and the compression of the double layer. Higher pH tends to increase PNP transport due to the enhanced deprotonation of surfaces. The release of retained PNPs under reduced IS and increased pH is limited because most of the PNPs were irreversibly captured in deep primary minima. The presence of physicochemical heterogeneities on solid surfaces can reduce PNP transport and increase the sensitivity of the transport to IS. Furthermore, variations in the hydrogen bonding when the two phosphates act as proton donors will result in different influences on PNP transport at the same IS. This study highlights the sensitivity of PNP transport to phosphates associated with the solution chemistries (e.g., IS and pH) and is helpful for better understanding the fate of PNPs and other colloidal contaminants in the subsurface environment.https://www.mdpi.com/1422-0067/23/17/9860plastic nanoparticlesphosphatessolution chemistryretentionrelease |
spellingShingle | Xingyu Liu Yan Liang Yongtao Peng Tingting Meng Liling Xu Pengcheng Dong Sensitivity of the Transport of Plastic Nanoparticles to Typical Phosphates Associated with Ionic Strength and Solution pH International Journal of Molecular Sciences plastic nanoparticles phosphates solution chemistry retention release |
title | Sensitivity of the Transport of Plastic Nanoparticles to Typical Phosphates Associated with Ionic Strength and Solution pH |
title_full | Sensitivity of the Transport of Plastic Nanoparticles to Typical Phosphates Associated with Ionic Strength and Solution pH |
title_fullStr | Sensitivity of the Transport of Plastic Nanoparticles to Typical Phosphates Associated with Ionic Strength and Solution pH |
title_full_unstemmed | Sensitivity of the Transport of Plastic Nanoparticles to Typical Phosphates Associated with Ionic Strength and Solution pH |
title_short | Sensitivity of the Transport of Plastic Nanoparticles to Typical Phosphates Associated with Ionic Strength and Solution pH |
title_sort | sensitivity of the transport of plastic nanoparticles to typical phosphates associated with ionic strength and solution ph |
topic | plastic nanoparticles phosphates solution chemistry retention release |
url | https://www.mdpi.com/1422-0067/23/17/9860 |
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