Investigation of pore water and soil extraction tests for characterizing the fate of poorly soluble metal-oxide nanoparticles

Detalhes bibliográficos
Autor(a) principal: Rodrigues, Sandra
Data de Publicação: 2021
Outros Autores: Bland, Garret D., Gao, Xiaoyu, Rodrigues, Sónia M., Lowry, Gregory V.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10773/30546
Resumo: Here we compared the efficiency of Cu extraction (dissolved + particulate) from two soils dosed with CuO nanoparticles (NPs) at 50 or 250 mg kg-1 by pore water collection, and single- and multi-step soil extraction tests. Pore water collection recovered low levels of Cu (<0.18%, regardless of soil type or Cu dose). Single soil extraction by either CaCl2 or DI water led to higher Cu recovery than pore water collection, but still <3% of total dose. These methods were useful for assessing the labile Cu ions pool. This fraction is controlled by Cu2+ dissolved from CuO NPs and it varies with time and soil type. Particulate Cu was poorly retrieved (<0.7%) by pore water extraction and by single-step soil extraction using CaCl2 solution or water. Multi-step extraction including dispersing and metal-chelating agents allowed for simultaneous characterization of dissolved Cu (total ionic Cu2+, 24-49% of dosed Cu), extractable CuO NPs (reversibly attached, 15-26% of dosed Cu), and non-extractable CuO NPs (irreversibly attached, 36-50% of dosed Cu), and it could describe the aging of NPs along 30 d. This method extracted a significantly higher concentration of Cu than pore water collection and was less sensitive to method parameters (e.g. filtration). This multi-step method can reduce pore water extraction-related factors that may confound the interpretation of environmental exposure data in NPs studies, and describe upper limits of both exchangeable Cu2+ and dispersible CuO NPs in soil that can potentially become bioavailable to plants and organisms and thus provide a sounder basis for risks evaluations.
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spelling Investigation of pore water and soil extraction tests for characterizing the fate of poorly soluble metal-oxide nanoparticlesNano-enabled agrochemicalsDissolutionAttachmentMulti-step extraction testHere we compared the efficiency of Cu extraction (dissolved + particulate) from two soils dosed with CuO nanoparticles (NPs) at 50 or 250 mg kg-1 by pore water collection, and single- and multi-step soil extraction tests. Pore water collection recovered low levels of Cu (<0.18%, regardless of soil type or Cu dose). Single soil extraction by either CaCl2 or DI water led to higher Cu recovery than pore water collection, but still <3% of total dose. These methods were useful for assessing the labile Cu ions pool. This fraction is controlled by Cu2+ dissolved from CuO NPs and it varies with time and soil type. Particulate Cu was poorly retrieved (<0.7%) by pore water extraction and by single-step soil extraction using CaCl2 solution or water. Multi-step extraction including dispersing and metal-chelating agents allowed for simultaneous characterization of dissolved Cu (total ionic Cu2+, 24-49% of dosed Cu), extractable CuO NPs (reversibly attached, 15-26% of dosed Cu), and non-extractable CuO NPs (irreversibly attached, 36-50% of dosed Cu), and it could describe the aging of NPs along 30 d. This method extracted a significantly higher concentration of Cu than pore water collection and was less sensitive to method parameters (e.g. filtration). This multi-step method can reduce pore water extraction-related factors that may confound the interpretation of environmental exposure data in NPs studies, and describe upper limits of both exchangeable Cu2+ and dispersible CuO NPs in soil that can potentially become bioavailable to plants and organisms and thus provide a sounder basis for risks evaluations.Elsevier2021-032021-03-01T00:00:00Z2023-03-31T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfapplication/pdfhttp://hdl.handle.net/10773/30546eng0045-653510.1016/j.chemosphere.2020.128885Rodrigues, SandraBland, Garret D.Gao, XiaoyuRodrigues, Sónia M.Lowry, Gregory V.info:eu-repo/semantics/embargoedAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-02-22T11:59:02Zoai:ria.ua.pt:10773/30546Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:02:37.311958Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Investigation of pore water and soil extraction tests for characterizing the fate of poorly soluble metal-oxide nanoparticles
title Investigation of pore water and soil extraction tests for characterizing the fate of poorly soluble metal-oxide nanoparticles
spellingShingle Investigation of pore water and soil extraction tests for characterizing the fate of poorly soluble metal-oxide nanoparticles
Rodrigues, Sandra
Nano-enabled agrochemicals
Dissolution
Attachment
Multi-step extraction test
title_short Investigation of pore water and soil extraction tests for characterizing the fate of poorly soluble metal-oxide nanoparticles
title_full Investigation of pore water and soil extraction tests for characterizing the fate of poorly soluble metal-oxide nanoparticles
title_fullStr Investigation of pore water and soil extraction tests for characterizing the fate of poorly soluble metal-oxide nanoparticles
title_full_unstemmed Investigation of pore water and soil extraction tests for characterizing the fate of poorly soluble metal-oxide nanoparticles
title_sort Investigation of pore water and soil extraction tests for characterizing the fate of poorly soluble metal-oxide nanoparticles
author Rodrigues, Sandra
author_facet Rodrigues, Sandra
Bland, Garret D.
Gao, Xiaoyu
Rodrigues, Sónia M.
Lowry, Gregory V.
author_role author
author2 Bland, Garret D.
Gao, Xiaoyu
Rodrigues, Sónia M.
Lowry, Gregory V.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Rodrigues, Sandra
Bland, Garret D.
Gao, Xiaoyu
Rodrigues, Sónia M.
Lowry, Gregory V.
dc.subject.por.fl_str_mv Nano-enabled agrochemicals
Dissolution
Attachment
Multi-step extraction test
topic Nano-enabled agrochemicals
Dissolution
Attachment
Multi-step extraction test
description Here we compared the efficiency of Cu extraction (dissolved + particulate) from two soils dosed with CuO nanoparticles (NPs) at 50 or 250 mg kg-1 by pore water collection, and single- and multi-step soil extraction tests. Pore water collection recovered low levels of Cu (<0.18%, regardless of soil type or Cu dose). Single soil extraction by either CaCl2 or DI water led to higher Cu recovery than pore water collection, but still <3% of total dose. These methods were useful for assessing the labile Cu ions pool. This fraction is controlled by Cu2+ dissolved from CuO NPs and it varies with time and soil type. Particulate Cu was poorly retrieved (<0.7%) by pore water extraction and by single-step soil extraction using CaCl2 solution or water. Multi-step extraction including dispersing and metal-chelating agents allowed for simultaneous characterization of dissolved Cu (total ionic Cu2+, 24-49% of dosed Cu), extractable CuO NPs (reversibly attached, 15-26% of dosed Cu), and non-extractable CuO NPs (irreversibly attached, 36-50% of dosed Cu), and it could describe the aging of NPs along 30 d. This method extracted a significantly higher concentration of Cu than pore water collection and was less sensitive to method parameters (e.g. filtration). This multi-step method can reduce pore water extraction-related factors that may confound the interpretation of environmental exposure data in NPs studies, and describe upper limits of both exchangeable Cu2+ and dispersible CuO NPs in soil that can potentially become bioavailable to plants and organisms and thus provide a sounder basis for risks evaluations.
publishDate 2021
dc.date.none.fl_str_mv 2021-03
2021-03-01T00:00:00Z
2023-03-31T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10773/30546
url http://hdl.handle.net/10773/30546
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0045-6535
10.1016/j.chemosphere.2020.128885
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dc.format.none.fl_str_mv application/pdf
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dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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