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dc.contributor.author
Cavallo, Jesica Anabel  
dc.contributor.author
Gomez, Cesar Gerardo  
dc.contributor.author
Strumia, Miriam Cristina  
dc.date.available
2019-09-25T17:02:04Z  
dc.date.issued
2010-08  
dc.identifier.citation
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  
dc.identifier.issn
1022-1352  
dc.identifier.uri
http://hdl.handle.net/11336/84411  
dc.description.abstract
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.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Wiley VCH Verlag  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Polypropylene Based  
dc.subject
Chitosan  
dc.subject
Methylene Blue  
dc.subject
Multilayers  
dc.subject.classification
Físico-Química, Ciencia de los Polímeros, Electroquímica  
dc.subject.classification
Ciencias Químicas  
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS  
dc.title
Formation of poly(propylene)-based biocomposite films and their use in the attachment of methylene blue  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2019-09-23T17:28:42Z  
dc.identifier.eissn
1521-3935  
dc.journal.volume
211  
dc.journal.number
16  
dc.journal.pagination
1793-1802  
dc.journal.pais
Alemania  
dc.journal.ciudad
Weinheim  
dc.description.fil
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  
dc.description.fil
Fil: Gomez, Cesar Gerardo. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Química Orgánica; Argentina  
dc.description.fil
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  
dc.journal.title
Macromolecular Chemistry And Physics  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/full/10.1002/macp.201000047  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1002/macp.201000047