Photochemical reduction of U(VI) in aqueous solution in the presence of 2-propanol
- Autores
- Salomone, Vanesa Natalia; Meichtry, Jorge Martin; Schinelli, Guillermo; Leyva de Guglielmino, Ana Gabriela; Litter, Marta Irene
- Año de publicación
- 2014
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The efficiency of the photochemical reduction of uranyl (UO22+) (0.25 mM, pH 3) was analyzed in theabsence and in the presence of 2-propanol (2-PrOH), evaluating the effect of anions (nitrate, acetate andperchlorate) and the use of quartz and glass photoreactors. A higher removal was observed under allconditions with the quartz photoreactor; the best system was that starting from uranyl nitrate, where a90% UO22+removal was attained after 15 min irradiation. In the absence of 2-PrOH, the acetate systemwas the only one where some U(VI) removal was observed (15% after 15 min in the quartz photoreactor)but, in the presence of the alcohol, the acetate system was the least reactive. Under irradiation, nitrateand acetate were consumed during the reaction, causing important effects on the uranyl conversion,while perchlorate was inactive. Uranium was removed from the system as a solid residue in the case ofnitrate- (as U(IV)) and perchlorate-containing systems (as U(VI)), while it remained in solution in thecase of the acetate systems. Mechanisms are proposed for the different conditions. The importance ofnitrate as a reducing agent of uranium species has not been previously reported. The use of uranyl nitrateand short-near UV?vis light seems to be the most advisable way of removing uranyl from solutions, inthe form of a stable precipitate.
Fil: Salomone, Vanesa Natalia. Comisión Nacional de Energía Atómica. Gerencia del Área de Seguridad Nuclear y Ambiente. Gerencia de Química (CAC); Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Meichtry, Jorge Martin. Comisión Nacional de Energía Atómica. Gerencia del Área de Seguridad Nuclear y Ambiente. Gerencia de Química (CAC); Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Schinelli, Guillermo. Comisión Nacional de Energía Atómica. Gerencia del Área de Seguridad Nuclear y Ambiente. Gerencia de Química (CAC); Argentina
Fil: Leyva de Guglielmino, Ana Gabriela. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes. Gerencia de Investigación y Aplicaciones; Argentina
Fil: Litter, Marta Irene. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica. Gerencia del Área de Seguridad Nuclear y Ambiente. Gerencia de Química (CAC); Argentina. Universidad Nacional de San Martín. Instituto de Investigación en Ingeniería Ambiental; Argentina - Materia
-
Photochemical reduction
U(VI)
U(IV)
2-Propanol - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/103941
Ver los metadatos del registro completo
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3498 |
network_name_str |
CONICET Digital (CONICET) |
spelling |
Photochemical reduction of U(VI) in aqueous solution in the presence of 2-propanolSalomone, Vanesa NataliaMeichtry, Jorge MartinSchinelli, GuillermoLeyva de Guglielmino, Ana GabrielaLitter, Marta IrenePhotochemical reductionU(VI)U(IV)2-Propanolhttps://purl.org/becyt/ford/1.5https://purl.org/becyt/ford/1The efficiency of the photochemical reduction of uranyl (UO22+) (0.25 mM, pH 3) was analyzed in theabsence and in the presence of 2-propanol (2-PrOH), evaluating the effect of anions (nitrate, acetate andperchlorate) and the use of quartz and glass photoreactors. A higher removal was observed under allconditions with the quartz photoreactor; the best system was that starting from uranyl nitrate, where a90% UO22+removal was attained after 15 min irradiation. In the absence of 2-PrOH, the acetate systemwas the only one where some U(VI) removal was observed (15% after 15 min in the quartz photoreactor)but, in the presence of the alcohol, the acetate system was the least reactive. Under irradiation, nitrateand acetate were consumed during the reaction, causing important effects on the uranyl conversion,while perchlorate was inactive. Uranium was removed from the system as a solid residue in the case ofnitrate- (as U(IV)) and perchlorate-containing systems (as U(VI)), while it remained in solution in thecase of the acetate systems. Mechanisms are proposed for the different conditions. The importance ofnitrate as a reducing agent of uranium species has not been previously reported. The use of uranyl nitrateand short-near UV?vis light seems to be the most advisable way of removing uranyl from solutions, inthe form of a stable precipitate.Fil: Salomone, Vanesa Natalia. Comisión Nacional de Energía Atómica. Gerencia del Área de Seguridad Nuclear y Ambiente. Gerencia de Química (CAC); Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Meichtry, Jorge Martin. Comisión Nacional de Energía Atómica. Gerencia del Área de Seguridad Nuclear y Ambiente. Gerencia de Química (CAC); Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Schinelli, Guillermo. Comisión Nacional de Energía Atómica. Gerencia del Área de Seguridad Nuclear y Ambiente. Gerencia de Química (CAC); ArgentinaFil: Leyva de Guglielmino, Ana Gabriela. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes. Gerencia de Investigación y Aplicaciones; ArgentinaFil: Litter, Marta Irene. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica. Gerencia del Área de Seguridad Nuclear y Ambiente. Gerencia de Química (CAC); Argentina. Universidad Nacional de San Martín. Instituto de Investigación en Ingeniería Ambiental; ArgentinaElsevier Science Sa2014-03info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/103941Salomone, Vanesa Natalia; Meichtry, Jorge Martin; Schinelli, Guillermo; Leyva de Guglielmino, Ana Gabriela; Litter, Marta Irene; Photochemical reduction of U(VI) in aqueous solution in the presence of 2-propanol; Elsevier Science Sa; Journal of Photochemistry and Photobiology A: Chemistry; 277; 3-2014; 19-261010-6030CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S1010603013005030info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jphotochem.2013.12.006info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:19:11Zoai:ri.conicet.gov.ar:11336/103941instacron: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:34982025-09-29 10:19:11.233CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Photochemical reduction of U(VI) in aqueous solution in the presence of 2-propanol |
title |
Photochemical reduction of U(VI) in aqueous solution in the presence of 2-propanol |
spellingShingle |
Photochemical reduction of U(VI) in aqueous solution in the presence of 2-propanol Salomone, Vanesa Natalia Photochemical reduction U(VI) U(IV) 2-Propanol |
title_short |
Photochemical reduction of U(VI) in aqueous solution in the presence of 2-propanol |
title_full |
Photochemical reduction of U(VI) in aqueous solution in the presence of 2-propanol |
title_fullStr |
Photochemical reduction of U(VI) in aqueous solution in the presence of 2-propanol |
title_full_unstemmed |
Photochemical reduction of U(VI) in aqueous solution in the presence of 2-propanol |
title_sort |
Photochemical reduction of U(VI) in aqueous solution in the presence of 2-propanol |
dc.creator.none.fl_str_mv |
Salomone, Vanesa Natalia Meichtry, Jorge Martin Schinelli, Guillermo Leyva de Guglielmino, Ana Gabriela Litter, Marta Irene |
author |
Salomone, Vanesa Natalia |
author_facet |
Salomone, Vanesa Natalia Meichtry, Jorge Martin Schinelli, Guillermo Leyva de Guglielmino, Ana Gabriela Litter, Marta Irene |
author_role |
author |
author2 |
Meichtry, Jorge Martin Schinelli, Guillermo Leyva de Guglielmino, Ana Gabriela Litter, Marta Irene |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
Photochemical reduction U(VI) U(IV) 2-Propanol |
topic |
Photochemical reduction U(VI) U(IV) 2-Propanol |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.5 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
The efficiency of the photochemical reduction of uranyl (UO22+) (0.25 mM, pH 3) was analyzed in theabsence and in the presence of 2-propanol (2-PrOH), evaluating the effect of anions (nitrate, acetate andperchlorate) and the use of quartz and glass photoreactors. A higher removal was observed under allconditions with the quartz photoreactor; the best system was that starting from uranyl nitrate, where a90% UO22+removal was attained after 15 min irradiation. In the absence of 2-PrOH, the acetate systemwas the only one where some U(VI) removal was observed (15% after 15 min in the quartz photoreactor)but, in the presence of the alcohol, the acetate system was the least reactive. Under irradiation, nitrateand acetate were consumed during the reaction, causing important effects on the uranyl conversion,while perchlorate was inactive. Uranium was removed from the system as a solid residue in the case ofnitrate- (as U(IV)) and perchlorate-containing systems (as U(VI)), while it remained in solution in thecase of the acetate systems. Mechanisms are proposed for the different conditions. The importance ofnitrate as a reducing agent of uranium species has not been previously reported. The use of uranyl nitrateand short-near UV?vis light seems to be the most advisable way of removing uranyl from solutions, inthe form of a stable precipitate. Fil: Salomone, Vanesa Natalia. Comisión Nacional de Energía Atómica. Gerencia del Área de Seguridad Nuclear y Ambiente. Gerencia de Química (CAC); Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Meichtry, Jorge Martin. Comisión Nacional de Energía Atómica. Gerencia del Área de Seguridad Nuclear y Ambiente. Gerencia de Química (CAC); Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Schinelli, Guillermo. Comisión Nacional de Energía Atómica. Gerencia del Área de Seguridad Nuclear y Ambiente. Gerencia de Química (CAC); Argentina Fil: Leyva de Guglielmino, Ana Gabriela. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes. Gerencia de Investigación y Aplicaciones; Argentina Fil: Litter, Marta Irene. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica. Gerencia del Área de Seguridad Nuclear y Ambiente. Gerencia de Química (CAC); Argentina. Universidad Nacional de San Martín. Instituto de Investigación en Ingeniería Ambiental; Argentina |
description |
The efficiency of the photochemical reduction of uranyl (UO22+) (0.25 mM, pH 3) was analyzed in theabsence and in the presence of 2-propanol (2-PrOH), evaluating the effect of anions (nitrate, acetate andperchlorate) and the use of quartz and glass photoreactors. A higher removal was observed under allconditions with the quartz photoreactor; the best system was that starting from uranyl nitrate, where a90% UO22+removal was attained after 15 min irradiation. In the absence of 2-PrOH, the acetate systemwas the only one where some U(VI) removal was observed (15% after 15 min in the quartz photoreactor)but, in the presence of the alcohol, the acetate system was the least reactive. Under irradiation, nitrateand acetate were consumed during the reaction, causing important effects on the uranyl conversion,while perchlorate was inactive. Uranium was removed from the system as a solid residue in the case ofnitrate- (as U(IV)) and perchlorate-containing systems (as U(VI)), while it remained in solution in thecase of the acetate systems. Mechanisms are proposed for the different conditions. The importance ofnitrate as a reducing agent of uranium species has not been previously reported. The use of uranyl nitrateand short-near UV?vis light seems to be the most advisable way of removing uranyl from solutions, inthe form of a stable precipitate. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-03 |
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/11336/103941 Salomone, Vanesa Natalia; Meichtry, Jorge Martin; Schinelli, Guillermo; Leyva de Guglielmino, Ana Gabriela; Litter, Marta Irene; Photochemical reduction of U(VI) in aqueous solution in the presence of 2-propanol; Elsevier Science Sa; Journal of Photochemistry and Photobiology A: Chemistry; 277; 3-2014; 19-26 1010-6030 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/103941 |
identifier_str_mv |
Salomone, Vanesa Natalia; Meichtry, Jorge Martin; Schinelli, Guillermo; Leyva de Guglielmino, Ana Gabriela; Litter, Marta Irene; Photochemical reduction of U(VI) in aqueous solution in the presence of 2-propanol; Elsevier Science Sa; Journal of Photochemistry and Photobiology A: Chemistry; 277; 3-2014; 19-26 1010-6030 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://www.sciencedirect.com/science/article/abs/pii/S1010603013005030 info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jphotochem.2013.12.006 |
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 application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier Science Sa |
publisher.none.fl_str_mv |
Elsevier Science Sa |
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) |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1844614161196122112 |
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13.070432 |