Degradation of the herbicides clomazone, paraquat and glyphosate by thermally activated peroxydisulfate.
- Autores
- Diaz Kirmser, Elena M.; Martire, Daniel Osvaldo; Gonzalez, Monica Cristina; Rosso, Janina Alejandra
- Año de publicación
- 2010
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Activated sodium peroxydisulfate has the potential to in situ destruct many organic contaminants because of the generation of the stronger oxidant sulfate radical. From photochemical activation of peroxydisulfate in flash-photolysis experiments, the bimolecular rate constants for the reaction of sulfate radical with glyphosate (1.6 108 M-1 s-1 ) and paraquat (1.2 109 M-1 s-1 ) at 25 C were obtained. Thermal activation of peroxydisulfate was shown to degrade the herbicides clomazone, paraquat, and glyphosate. Although the herbicide degradation was observed to take place in less than 1 h, the mineralization of the organic carbon required longer reaction times, because of the formation of stable organic intermediates. For similar initial total organic carbon (TOC) values, TOC profiles were similar for experiments with different substrates (the herbicides, humic acids, and a mixture of glyphosate and humic acids), which indicates that the mineralization of all of the samples is limited by the production of SO4 • - radicals. A linear correlation between the initial amount of SO4 • - needed per mole of C and the average oxidation state was found.
Fil: Diaz Kirmser, Elena M.. Universidad Nacional de Asunción; Paraguay
Fil: Martire, Daniel Osvaldo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina
Fil: Gonzalez, Monica Cristina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina
Fil: Rosso, Janina Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina - Materia
-
PEROXYDISULFATE
SULFATE RADICAL
GLYPHOSATE
CLOMAZONE - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/278655
Ver los metadatos del registro completo
| id |
CONICETDig_07e27122d7d7e661bc4ce65667e13eae |
|---|---|
| oai_identifier_str |
oai:ri.conicet.gov.ar:11336/278655 |
| network_acronym_str |
CONICETDig |
| repository_id_str |
3498 |
| network_name_str |
CONICET Digital (CONICET) |
| spelling |
Degradation of the herbicides clomazone, paraquat and glyphosate by thermally activated peroxydisulfate.Diaz Kirmser, Elena M.Martire, Daniel OsvaldoGonzalez, Monica CristinaRosso, Janina AlejandraPEROXYDISULFATESULFATE RADICALGLYPHOSATECLOMAZONEhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1Activated sodium peroxydisulfate has the potential to in situ destruct many organic contaminants because of the generation of the stronger oxidant sulfate radical. From photochemical activation of peroxydisulfate in flash-photolysis experiments, the bimolecular rate constants for the reaction of sulfate radical with glyphosate (1.6 108 M-1 s-1 ) and paraquat (1.2 109 M-1 s-1 ) at 25 C were obtained. Thermal activation of peroxydisulfate was shown to degrade the herbicides clomazone, paraquat, and glyphosate. Although the herbicide degradation was observed to take place in less than 1 h, the mineralization of the organic carbon required longer reaction times, because of the formation of stable organic intermediates. For similar initial total organic carbon (TOC) values, TOC profiles were similar for experiments with different substrates (the herbicides, humic acids, and a mixture of glyphosate and humic acids), which indicates that the mineralization of all of the samples is limited by the production of SO4 • - radicals. A linear correlation between the initial amount of SO4 • - needed per mole of C and the average oxidation state was found.Fil: Diaz Kirmser, Elena M.. Universidad Nacional de Asunción; ParaguayFil: Martire, Daniel Osvaldo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; ArgentinaFil: Gonzalez, Monica Cristina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; ArgentinaFil: Rosso, Janina Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; ArgentinaAmerican Chemical Society2010-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/278655Diaz Kirmser, Elena M.; Martire, Daniel Osvaldo; Gonzalez, Monica Cristina; Rosso, Janina Alejandra; Degradation of the herbicides clomazone, paraquat and glyphosate by thermally activated peroxydisulfate.; American Chemical Society; Journal of Agricultural and Food Chemistry; 58; 24; 11-2010; 12858-128620021-8561CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/jf103054hinfo:eu-repo/semantics/altIdentifier/doi/10.1021/jf103054hinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2026-02-26T09:59:49Zoai:ri.conicet.gov.ar:11336/278655instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982026-02-26 09:59:49.577CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Degradation of the herbicides clomazone, paraquat and glyphosate by thermally activated peroxydisulfate. |
| title |
Degradation of the herbicides clomazone, paraquat and glyphosate by thermally activated peroxydisulfate. |
| spellingShingle |
Degradation of the herbicides clomazone, paraquat and glyphosate by thermally activated peroxydisulfate. Diaz Kirmser, Elena M. PEROXYDISULFATE SULFATE RADICAL GLYPHOSATE CLOMAZONE |
| title_short |
Degradation of the herbicides clomazone, paraquat and glyphosate by thermally activated peroxydisulfate. |
| title_full |
Degradation of the herbicides clomazone, paraquat and glyphosate by thermally activated peroxydisulfate. |
| title_fullStr |
Degradation of the herbicides clomazone, paraquat and glyphosate by thermally activated peroxydisulfate. |
| title_full_unstemmed |
Degradation of the herbicides clomazone, paraquat and glyphosate by thermally activated peroxydisulfate. |
| title_sort |
Degradation of the herbicides clomazone, paraquat and glyphosate by thermally activated peroxydisulfate. |
| dc.creator.none.fl_str_mv |
Diaz Kirmser, Elena M. Martire, Daniel Osvaldo Gonzalez, Monica Cristina Rosso, Janina Alejandra |
| author |
Diaz Kirmser, Elena M. |
| author_facet |
Diaz Kirmser, Elena M. Martire, Daniel Osvaldo Gonzalez, Monica Cristina Rosso, Janina Alejandra |
| author_role |
author |
| author2 |
Martire, Daniel Osvaldo Gonzalez, Monica Cristina Rosso, Janina Alejandra |
| author2_role |
author author author |
| dc.subject.none.fl_str_mv |
PEROXYDISULFATE SULFATE RADICAL GLYPHOSATE CLOMAZONE |
| topic |
PEROXYDISULFATE SULFATE RADICAL GLYPHOSATE CLOMAZONE |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
| dc.description.none.fl_txt_mv |
Activated sodium peroxydisulfate has the potential to in situ destruct many organic contaminants because of the generation of the stronger oxidant sulfate radical. From photochemical activation of peroxydisulfate in flash-photolysis experiments, the bimolecular rate constants for the reaction of sulfate radical with glyphosate (1.6 108 M-1 s-1 ) and paraquat (1.2 109 M-1 s-1 ) at 25 C were obtained. Thermal activation of peroxydisulfate was shown to degrade the herbicides clomazone, paraquat, and glyphosate. Although the herbicide degradation was observed to take place in less than 1 h, the mineralization of the organic carbon required longer reaction times, because of the formation of stable organic intermediates. For similar initial total organic carbon (TOC) values, TOC profiles were similar for experiments with different substrates (the herbicides, humic acids, and a mixture of glyphosate and humic acids), which indicates that the mineralization of all of the samples is limited by the production of SO4 • - radicals. A linear correlation between the initial amount of SO4 • - needed per mole of C and the average oxidation state was found. Fil: Diaz Kirmser, Elena M.. Universidad Nacional de Asunción; Paraguay Fil: Martire, Daniel Osvaldo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina Fil: Gonzalez, Monica Cristina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina Fil: Rosso, Janina Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina |
| description |
Activated sodium peroxydisulfate has the potential to in situ destruct many organic contaminants because of the generation of the stronger oxidant sulfate radical. From photochemical activation of peroxydisulfate in flash-photolysis experiments, the bimolecular rate constants for the reaction of sulfate radical with glyphosate (1.6 108 M-1 s-1 ) and paraquat (1.2 109 M-1 s-1 ) at 25 C were obtained. Thermal activation of peroxydisulfate was shown to degrade the herbicides clomazone, paraquat, and glyphosate. Although the herbicide degradation was observed to take place in less than 1 h, the mineralization of the organic carbon required longer reaction times, because of the formation of stable organic intermediates. For similar initial total organic carbon (TOC) values, TOC profiles were similar for experiments with different substrates (the herbicides, humic acids, and a mixture of glyphosate and humic acids), which indicates that the mineralization of all of the samples is limited by the production of SO4 • - radicals. A linear correlation between the initial amount of SO4 • - needed per mole of C and the average oxidation state was found. |
| publishDate |
2010 |
| dc.date.none.fl_str_mv |
2010-11 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/278655 Diaz Kirmser, Elena M.; Martire, Daniel Osvaldo; Gonzalez, Monica Cristina; Rosso, Janina Alejandra; Degradation of the herbicides clomazone, paraquat and glyphosate by thermally activated peroxydisulfate.; American Chemical Society; Journal of Agricultural and Food Chemistry; 58; 24; 11-2010; 12858-12862 0021-8561 CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/278655 |
| identifier_str_mv |
Diaz Kirmser, Elena M.; Martire, Daniel Osvaldo; Gonzalez, Monica Cristina; Rosso, Janina Alejandra; Degradation of the herbicides clomazone, paraquat and glyphosate by thermally activated peroxydisulfate.; American Chemical Society; Journal of Agricultural and Food Chemistry; 58; 24; 11-2010; 12858-12862 0021-8561 CONICET Digital CONICET |
| dc.language.none.fl_str_mv |
eng |
| language |
eng |
| dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/jf103054h info:eu-repo/semantics/altIdentifier/doi/10.1021/jf103054h |
| dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
| eu_rights_str_mv |
openAccess |
| rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
| dc.format.none.fl_str_mv |
application/pdf application/pdf application/pdf |
| dc.publisher.none.fl_str_mv |
American Chemical Society |
| publisher.none.fl_str_mv |
American Chemical Society |
| dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
| reponame_str |
CONICET Digital (CONICET) |
| collection |
CONICET Digital (CONICET) |
| instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
| repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
| repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
| _version_ |
1858304882020188160 |
| score |
13.176822 |