Formation of poly(propylene)-based biocomposite films and their use in the attachment of methylene blue

Autores
Cavallo, Jesica Anabel; Gomez, Cesar Gerardo; Strumia, Miriam Cristina
Año de publicación
2010
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Biocomposite PP-g-PAAc-CS films based on PP were generated and utilized as support of methylene blue, a thiazidic dye. Using a photograft polymerization of acrylic acid, the PP film was functionalized with carboxyl groups (PP-g-PAAc), which attached chitosan by electrostatic bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. methylene blue, a thiazidic dye. Using a photograft polymerization of acrylic acid, the PP film was functionalized with carboxyl groups (PP-g-PAAc), which attached chitosan by electrostatic bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. -g-PAAc-CS films based on PP were generated and utilized as support of methylene blue, a thiazidic dye. Using a photograft polymerization of acrylic acid, the PP film was functionalized with carboxyl groups (PP-g-PAAc), which attached chitosan by electrostatic bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. -g-PAAc), which attached chitosan by electrostatic bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree.
Fil: Cavallo, Jesica Anabel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina
Fil: Gomez, Cesar Gerardo. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Química Orgánica; Argentina
Fil: Strumia, Miriam Cristina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina
Materia
Polypropylene Based
Chitosan
Methylene Blue
Multilayers
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/84411

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spelling Formation of poly(propylene)-based biocomposite films and their use in the attachment of methylene blueCavallo, Jesica AnabelGomez, Cesar GerardoStrumia, Miriam CristinaPolypropylene BasedChitosanMethylene BlueMultilayershttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1Biocomposite PP-g-PAAc-CS films based on PP were generated and utilized as support of methylene blue, a thiazidic dye. Using a photograft polymerization of acrylic acid, the PP film was functionalized with carboxyl groups (PP-g-PAAc), which attached chitosan by electrostatic bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. methylene blue, a thiazidic dye. Using a photograft polymerization of acrylic acid, the PP film was functionalized with carboxyl groups (PP-g-PAAc), which attached chitosan by electrostatic bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. -g-PAAc-CS films based on PP were generated and utilized as support of methylene blue, a thiazidic dye. Using a photograft polymerization of acrylic acid, the PP film was functionalized with carboxyl groups (PP-g-PAAc), which attached chitosan by electrostatic bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. -g-PAAc), which attached chitosan by electrostatic bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree.Fil: Cavallo, Jesica Anabel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; ArgentinaFil: Gomez, Cesar Gerardo. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Química Orgánica; ArgentinaFil: Strumia, Miriam Cristina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; ArgentinaWiley VCH Verlag2010-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/84411Cavallo, Jesica Anabel; Gomez, Cesar Gerardo; Strumia, Miriam Cristina; Formation of poly(propylene)-based biocomposite films and their use in the attachment of methylene blue; Wiley VCH Verlag; Macromolecular Chemistry And Physics; 211; 16; 8-2010; 1793-18021022-13521521-3935CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/full/10.1002/macp.201000047info:eu-repo/semantics/altIdentifier/doi/10.1002/macp.201000047info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:31:45Zoai:ri.conicet.gov.ar:11336/84411instacron: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 10:31:45.791CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Formation of poly(propylene)-based biocomposite films and their use in the attachment of methylene blue
title Formation of poly(propylene)-based biocomposite films and their use in the attachment of methylene blue
spellingShingle Formation of poly(propylene)-based biocomposite films and their use in the attachment of methylene blue
Cavallo, Jesica Anabel
Polypropylene Based
Chitosan
Methylene Blue
Multilayers
title_short Formation of poly(propylene)-based biocomposite films and their use in the attachment of methylene blue
title_full Formation of poly(propylene)-based biocomposite films and their use in the attachment of methylene blue
title_fullStr Formation of poly(propylene)-based biocomposite films and their use in the attachment of methylene blue
title_full_unstemmed Formation of poly(propylene)-based biocomposite films and their use in the attachment of methylene blue
title_sort Formation of poly(propylene)-based biocomposite films and their use in the attachment of methylene blue
dc.creator.none.fl_str_mv Cavallo, Jesica Anabel
Gomez, Cesar Gerardo
Strumia, Miriam Cristina
author Cavallo, Jesica Anabel
author_facet Cavallo, Jesica Anabel
Gomez, Cesar Gerardo
Strumia, Miriam Cristina
author_role author
author2 Gomez, Cesar Gerardo
Strumia, Miriam Cristina
author2_role author
author
dc.subject.none.fl_str_mv Polypropylene Based
Chitosan
Methylene Blue
Multilayers
topic Polypropylene Based
Chitosan
Methylene Blue
Multilayers
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Biocomposite PP-g-PAAc-CS films based on PP were generated and utilized as support of methylene blue, a thiazidic dye. Using a photograft polymerization of acrylic acid, the PP film was functionalized with carboxyl groups (PP-g-PAAc), which attached chitosan by electrostatic bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. methylene blue, a thiazidic dye. Using a photograft polymerization of acrylic acid, the PP film was functionalized with carboxyl groups (PP-g-PAAc), which attached chitosan by electrostatic bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. -g-PAAc-CS films based on PP were generated and utilized as support of methylene blue, a thiazidic dye. Using a photograft polymerization of acrylic acid, the PP film was functionalized with carboxyl groups (PP-g-PAAc), which attached chitosan by electrostatic bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. -g-PAAc), which attached chitosan by electrostatic bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree.
Fil: Cavallo, Jesica Anabel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina
Fil: Gomez, Cesar Gerardo. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Química Orgánica; Argentina
Fil: Strumia, Miriam Cristina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina
description Biocomposite PP-g-PAAc-CS films based on PP were generated and utilized as support of methylene blue, a thiazidic dye. Using a photograft polymerization of acrylic acid, the PP film was functionalized with carboxyl groups (PP-g-PAAc), which attached chitosan by electrostatic bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. methylene blue, a thiazidic dye. Using a photograft polymerization of acrylic acid, the PP film was functionalized with carboxyl groups (PP-g-PAAc), which attached chitosan by electrostatic bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. -g-PAAc-CS films based on PP were generated and utilized as support of methylene blue, a thiazidic dye. Using a photograft polymerization of acrylic acid, the PP film was functionalized with carboxyl groups (PP-g-PAAc), which attached chitosan by electrostatic bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. -g-PAAc), which attached chitosan by electrostatic bond. A longer poly(acrylic acid) chain or a higher CS immobilization temperature led to a higher chain interpenetration and crosslinking reaction. Immobilized MB confirmed to possess redox activity from its reaction with ascorbic acid, where the dye decomposition rate (R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree. interpenetration, then decreasing with the increase in the crosslinking degree. R0d) increases together with the chain interpenetration, then decreasing with the increase in the crosslinking degree.
publishDate 2010
dc.date.none.fl_str_mv 2010-08
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/11336/84411
Cavallo, Jesica Anabel; Gomez, Cesar Gerardo; Strumia, Miriam Cristina; Formation of poly(propylene)-based biocomposite films and their use in the attachment of methylene blue; Wiley VCH Verlag; Macromolecular Chemistry And Physics; 211; 16; 8-2010; 1793-1802
1022-1352
1521-3935
CONICET Digital
CONICET
url http://hdl.handle.net/11336/84411
identifier_str_mv Cavallo, Jesica Anabel; Gomez, Cesar Gerardo; Strumia, Miriam Cristina; Formation of poly(propylene)-based biocomposite films and their use in the attachment of methylene blue; Wiley VCH Verlag; Macromolecular Chemistry And Physics; 211; 16; 8-2010; 1793-1802
1022-1352
1521-3935
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://onlinelibrary.wiley.com/doi/full/10.1002/macp.201000047
info:eu-repo/semantics/altIdentifier/doi/10.1002/macp.201000047
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
dc.publisher.none.fl_str_mv Wiley VCH Verlag
publisher.none.fl_str_mv Wiley VCH Verlag
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
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reponame_str CONICET Digital (CONICET)
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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
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