Investigation of pore water and soil extraction tests for characterizing the fate of poorly soluble metal-oxide nanoparticles
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , |
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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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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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 |
status_str |
publishedVersion |
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 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/embargoedAccess |
eu_rights_str_mv |
embargoedAccess |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
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 instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
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 |
repository.mail.fl_str_mv |
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1799137681693736960 |