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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/84411
Ver los metadatos del registro completo
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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) 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 |
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1844614329206308864 |
score |
13.070432 |