Visible light photopolymerization in BHDC reverse micelles: laser flash photolysis study of the photoinitiating mechanism

Autores
Porcal, Gabriela Valeria; Arbeloa, Ernesto Maximiliano; Chesta, Carlos Alberto; Bertolotti, Sonia Graciela; Previtali, Carlos Mario
Año de publicación
2013
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The photopolymerization of acrylamide (AA) in reverse micelles (RMs) of benzyl hexadecyl dimethylammonium chloride (BHDC) was investigated. The polymerization was performed by irradiation in the 500 nm region of the spectrum, employing as photoinitiating system the synthetic dye safranine-O and triethanolamine (TEOA) as co-initiator. The characterization of the nanoparticles of polyacrylamide was done by dynamic light scattering. Molecular weight determinations were carried out by viscosimetry. Small nanoparticles of polyacrylamide are formed with a low polydispersity and a molecular weight close to 106. The results were compared with those in AOT (sodium bis(2-ethylhexyl) sulfosuccinate) RMs. Laser flash photolysis was used to investigate the photoinitiating mechanism. The maximum of the T–T absorption spectra in RMs confirms that, in spite of its positive charge, the dyes remain at the interface co-micellizing with BHDC. The triplet lifetime is much longer in the RMs than in homogeneous organic solvents. The triplet quenching by TEOA was very much more effective in the RMs than in a homogeneous solvent. The quantum yield of formation of active radicals was evaluated from the transient absorption spectra. It was concluded that they are generated by an intermicellar electron transfer process followed by an intramicellar proton transfer reaction. The quantum yield was found to be 0.2 ± 0.02. A similar radical yield in a homogeneous solvent requires an amine concentration near 50 times higher.
Fil: Porcal, Gabriela Valeria. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Arbeloa, Ernesto Maximiliano. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Chesta, Carlos Alberto. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Bertolotti, Sonia Graciela. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Previtali, Carlos Mario. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Materia
Visible Photopolymerization
Safranine
Microemulsion Polymerization
Reverse Micelles
Triplet Quenching
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/23028

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network_name_str CONICET Digital (CONICET)
spelling Visible light photopolymerization in BHDC reverse micelles: laser flash photolysis study of the photoinitiating mechanismPorcal, Gabriela ValeriaArbeloa, Ernesto MaximilianoChesta, Carlos AlbertoBertolotti, Sonia GracielaPrevitali, Carlos MarioVisible PhotopolymerizationSafranineMicroemulsion PolymerizationReverse MicellesTriplet Quenchinghttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The photopolymerization of acrylamide (AA) in reverse micelles (RMs) of benzyl hexadecyl dimethylammonium chloride (BHDC) was investigated. The polymerization was performed by irradiation in the 500 nm region of the spectrum, employing as photoinitiating system the synthetic dye safranine-O and triethanolamine (TEOA) as co-initiator. The characterization of the nanoparticles of polyacrylamide was done by dynamic light scattering. Molecular weight determinations were carried out by viscosimetry. Small nanoparticles of polyacrylamide are formed with a low polydispersity and a molecular weight close to 106. The results were compared with those in AOT (sodium bis(2-ethylhexyl) sulfosuccinate) RMs. Laser flash photolysis was used to investigate the photoinitiating mechanism. The maximum of the T–T absorption spectra in RMs confirms that, in spite of its positive charge, the dyes remain at the interface co-micellizing with BHDC. The triplet lifetime is much longer in the RMs than in homogeneous organic solvents. The triplet quenching by TEOA was very much more effective in the RMs than in a homogeneous solvent. The quantum yield of formation of active radicals was evaluated from the transient absorption spectra. It was concluded that they are generated by an intermicellar electron transfer process followed by an intramicellar proton transfer reaction. The quantum yield was found to be 0.2 ± 0.02. A similar radical yield in a homogeneous solvent requires an amine concentration near 50 times higher.Fil: Porcal, Gabriela Valeria. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Arbeloa, Ernesto Maximiliano. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Chesta, Carlos Alberto. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Bertolotti, Sonia Graciela. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Previtali, Carlos Mario. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaElsevier Science2013-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/23028Porcal, Gabriela Valeria; Arbeloa, Ernesto Maximiliano; Chesta, Carlos Alberto; Bertolotti, Sonia Graciela; Previtali, Carlos Mario; Visible light photopolymerization in BHDC reverse micelles: laser flash photolysis study of the photoinitiating mechanism; Elsevier Science; Journal of Photochemistry and Photobiology A: Chemistry; 257; 2-2013; 60-651010-6030CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.jphotochem.2013.01.017info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S1010603013000439info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:57:23Zoai:ri.conicet.gov.ar:11336/23028instacron: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:34982025-09-03 09:57:25.089CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Visible light photopolymerization in BHDC reverse micelles: laser flash photolysis study of the photoinitiating mechanism
title Visible light photopolymerization in BHDC reverse micelles: laser flash photolysis study of the photoinitiating mechanism
spellingShingle Visible light photopolymerization in BHDC reverse micelles: laser flash photolysis study of the photoinitiating mechanism
Porcal, Gabriela Valeria
Visible Photopolymerization
Safranine
Microemulsion Polymerization
Reverse Micelles
Triplet Quenching
title_short Visible light photopolymerization in BHDC reverse micelles: laser flash photolysis study of the photoinitiating mechanism
title_full Visible light photopolymerization in BHDC reverse micelles: laser flash photolysis study of the photoinitiating mechanism
title_fullStr Visible light photopolymerization in BHDC reverse micelles: laser flash photolysis study of the photoinitiating mechanism
title_full_unstemmed Visible light photopolymerization in BHDC reverse micelles: laser flash photolysis study of the photoinitiating mechanism
title_sort Visible light photopolymerization in BHDC reverse micelles: laser flash photolysis study of the photoinitiating mechanism
dc.creator.none.fl_str_mv Porcal, Gabriela Valeria
Arbeloa, Ernesto Maximiliano
Chesta, Carlos Alberto
Bertolotti, Sonia Graciela
Previtali, Carlos Mario
author Porcal, Gabriela Valeria
author_facet Porcal, Gabriela Valeria
Arbeloa, Ernesto Maximiliano
Chesta, Carlos Alberto
Bertolotti, Sonia Graciela
Previtali, Carlos Mario
author_role author
author2 Arbeloa, Ernesto Maximiliano
Chesta, Carlos Alberto
Bertolotti, Sonia Graciela
Previtali, Carlos Mario
author2_role author
author
author
author
dc.subject.none.fl_str_mv Visible Photopolymerization
Safranine
Microemulsion Polymerization
Reverse Micelles
Triplet Quenching
topic Visible Photopolymerization
Safranine
Microemulsion Polymerization
Reverse Micelles
Triplet Quenching
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The photopolymerization of acrylamide (AA) in reverse micelles (RMs) of benzyl hexadecyl dimethylammonium chloride (BHDC) was investigated. The polymerization was performed by irradiation in the 500 nm region of the spectrum, employing as photoinitiating system the synthetic dye safranine-O and triethanolamine (TEOA) as co-initiator. The characterization of the nanoparticles of polyacrylamide was done by dynamic light scattering. Molecular weight determinations were carried out by viscosimetry. Small nanoparticles of polyacrylamide are formed with a low polydispersity and a molecular weight close to 106. The results were compared with those in AOT (sodium bis(2-ethylhexyl) sulfosuccinate) RMs. Laser flash photolysis was used to investigate the photoinitiating mechanism. The maximum of the T–T absorption spectra in RMs confirms that, in spite of its positive charge, the dyes remain at the interface co-micellizing with BHDC. The triplet lifetime is much longer in the RMs than in homogeneous organic solvents. The triplet quenching by TEOA was very much more effective in the RMs than in a homogeneous solvent. The quantum yield of formation of active radicals was evaluated from the transient absorption spectra. It was concluded that they are generated by an intermicellar electron transfer process followed by an intramicellar proton transfer reaction. The quantum yield was found to be 0.2 ± 0.02. A similar radical yield in a homogeneous solvent requires an amine concentration near 50 times higher.
Fil: Porcal, Gabriela Valeria. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Arbeloa, Ernesto Maximiliano. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Chesta, Carlos Alberto. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Bertolotti, Sonia Graciela. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Previtali, Carlos Mario. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
description The photopolymerization of acrylamide (AA) in reverse micelles (RMs) of benzyl hexadecyl dimethylammonium chloride (BHDC) was investigated. The polymerization was performed by irradiation in the 500 nm region of the spectrum, employing as photoinitiating system the synthetic dye safranine-O and triethanolamine (TEOA) as co-initiator. The characterization of the nanoparticles of polyacrylamide was done by dynamic light scattering. Molecular weight determinations were carried out by viscosimetry. Small nanoparticles of polyacrylamide are formed with a low polydispersity and a molecular weight close to 106. The results were compared with those in AOT (sodium bis(2-ethylhexyl) sulfosuccinate) RMs. Laser flash photolysis was used to investigate the photoinitiating mechanism. The maximum of the T–T absorption spectra in RMs confirms that, in spite of its positive charge, the dyes remain at the interface co-micellizing with BHDC. The triplet lifetime is much longer in the RMs than in homogeneous organic solvents. The triplet quenching by TEOA was very much more effective in the RMs than in a homogeneous solvent. The quantum yield of formation of active radicals was evaluated from the transient absorption spectra. It was concluded that they are generated by an intermicellar electron transfer process followed by an intramicellar proton transfer reaction. The quantum yield was found to be 0.2 ± 0.02. A similar radical yield in a homogeneous solvent requires an amine concentration near 50 times higher.
publishDate 2013
dc.date.none.fl_str_mv 2013-02
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/11336/23028
Porcal, Gabriela Valeria; Arbeloa, Ernesto Maximiliano; Chesta, Carlos Alberto; Bertolotti, Sonia Graciela; Previtali, Carlos Mario; Visible light photopolymerization in BHDC reverse micelles: laser flash photolysis study of the photoinitiating mechanism; Elsevier Science; Journal of Photochemistry and Photobiology A: Chemistry; 257; 2-2013; 60-65
1010-6030
CONICET Digital
CONICET
url http://hdl.handle.net/11336/23028
identifier_str_mv Porcal, Gabriela Valeria; Arbeloa, Ernesto Maximiliano; Chesta, Carlos Alberto; Bertolotti, Sonia Graciela; Previtali, Carlos Mario; Visible light photopolymerization in BHDC reverse micelles: laser flash photolysis study of the photoinitiating mechanism; Elsevier Science; Journal of Photochemistry and Photobiology A: Chemistry; 257; 2-2013; 60-65
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/doi/10.1016/j.jphotochem.2013.01.017
info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S1010603013000439
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
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application/pdf
application/pdf
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dc.publisher.none.fl_str_mv Elsevier Science
publisher.none.fl_str_mv Elsevier Science
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instname:Consejo Nacional de Investigaciones Científicas y Técnicas
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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
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