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Yttrium Residues in MWCNT Enable Assessment of MWCNT Removal during Wastewater Treatment

Many analytical techniques have limited sensitivity to quantify multi-walled carbon nanotubes (MWCNTs) at environmentally relevant exposure concentrations in wastewaters. We found that trace metals (e.g., Y, Co, Fe) used in MWCNT synthesis correlated with MWCNT concentrations. Because of low backgro...

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Autores principales: Kidd, Justin, Bi, Yuqiang, Hanigan, David, Herckes, Pierre, Westerhoff, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6566316/
https://www.ncbi.nlm.nih.gov/pubmed/31052363
http://dx.doi.org/10.3390/nano9050670
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author Kidd, Justin
Bi, Yuqiang
Hanigan, David
Herckes, Pierre
Westerhoff, Paul
author_facet Kidd, Justin
Bi, Yuqiang
Hanigan, David
Herckes, Pierre
Westerhoff, Paul
author_sort Kidd, Justin
collection PubMed
description Many analytical techniques have limited sensitivity to quantify multi-walled carbon nanotubes (MWCNTs) at environmentally relevant exposure concentrations in wastewaters. We found that trace metals (e.g., Y, Co, Fe) used in MWCNT synthesis correlated with MWCNT concentrations. Because of low background yttrium (Y) concentrations in wastewater, Y was used to track MWCNT removal by wastewater biomass. Transmission electron microscopy (TEM) imaging and dissolution studies indicated that the residual trace metals were strongly embedded within the MWCNTs. For our specific MWCNT, Y concentration in MWCNTs was 76 µg g(−1), and single particle mode inductively coupled plasma mass spectrometry (spICP-MS) was shown viable to detect Y-associated MWCNTs. The detection limit of the specific MWCNTs was 0.82 µg L(−1) using Y as a surrogate, compared with >100 µg L(−1) for other techniques applied for MWCNT quantification in wastewater biomass. MWCNT removal at wastewater treatment plants (WWTPs) was assessed by dosing MWCNTs (100 µg L(−1)) in water containing a range of biomass concentrations obtained from wastewater return activated sludge (RAS) collected from a local WWTP. Using high volume to surface area reactors (to limit artifacts of MWCNT loss due to adsorption to vessel walls) and adding 5 g L(−1) of total suspended solids (TSS) of RAS (3-h mixing) reduced the MWCNT concentrations from 100 µg L(−1) to 2 µg L(−1). The results provide an environmentally relevant insight into the fate of MWCNTs across their end of life cycle and aid in regulatory permits that require estimates of engineered nanomaterial removal at WWTPs upon accidental release into sewers from manufacturing facilities.
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spelling pubmed-65663162019-06-17 Yttrium Residues in MWCNT Enable Assessment of MWCNT Removal during Wastewater Treatment Kidd, Justin Bi, Yuqiang Hanigan, David Herckes, Pierre Westerhoff, Paul Nanomaterials (Basel) Article Many analytical techniques have limited sensitivity to quantify multi-walled carbon nanotubes (MWCNTs) at environmentally relevant exposure concentrations in wastewaters. We found that trace metals (e.g., Y, Co, Fe) used in MWCNT synthesis correlated with MWCNT concentrations. Because of low background yttrium (Y) concentrations in wastewater, Y was used to track MWCNT removal by wastewater biomass. Transmission electron microscopy (TEM) imaging and dissolution studies indicated that the residual trace metals were strongly embedded within the MWCNTs. For our specific MWCNT, Y concentration in MWCNTs was 76 µg g(−1), and single particle mode inductively coupled plasma mass spectrometry (spICP-MS) was shown viable to detect Y-associated MWCNTs. The detection limit of the specific MWCNTs was 0.82 µg L(−1) using Y as a surrogate, compared with >100 µg L(−1) for other techniques applied for MWCNT quantification in wastewater biomass. MWCNT removal at wastewater treatment plants (WWTPs) was assessed by dosing MWCNTs (100 µg L(−1)) in water containing a range of biomass concentrations obtained from wastewater return activated sludge (RAS) collected from a local WWTP. Using high volume to surface area reactors (to limit artifacts of MWCNT loss due to adsorption to vessel walls) and adding 5 g L(−1) of total suspended solids (TSS) of RAS (3-h mixing) reduced the MWCNT concentrations from 100 µg L(−1) to 2 µg L(−1). The results provide an environmentally relevant insight into the fate of MWCNTs across their end of life cycle and aid in regulatory permits that require estimates of engineered nanomaterial removal at WWTPs upon accidental release into sewers from manufacturing facilities. MDPI 2019-05-01 /pmc/articles/PMC6566316/ /pubmed/31052363 http://dx.doi.org/10.3390/nano9050670 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kidd, Justin
Bi, Yuqiang
Hanigan, David
Herckes, Pierre
Westerhoff, Paul
Yttrium Residues in MWCNT Enable Assessment of MWCNT Removal during Wastewater Treatment
title Yttrium Residues in MWCNT Enable Assessment of MWCNT Removal during Wastewater Treatment
title_full Yttrium Residues in MWCNT Enable Assessment of MWCNT Removal during Wastewater Treatment
title_fullStr Yttrium Residues in MWCNT Enable Assessment of MWCNT Removal during Wastewater Treatment
title_full_unstemmed Yttrium Residues in MWCNT Enable Assessment of MWCNT Removal during Wastewater Treatment
title_short Yttrium Residues in MWCNT Enable Assessment of MWCNT Removal during Wastewater Treatment
title_sort yttrium residues in mwcnt enable assessment of mwcnt removal during wastewater treatment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6566316/
https://www.ncbi.nlm.nih.gov/pubmed/31052363
http://dx.doi.org/10.3390/nano9050670
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