SYNTHESIS AND CHARACTERIZATION OF NEW THERMOSENSITIVE GRAFT COPOLYMERS FROM N-ISOPROPYLACRYLAMIDE AND 2-METHYL-2-OXAZOLINE MACROMONOMERS
Descripción del Articulo
New graft copolymers were synthesized from the free radical polymerization of N-isopropylacrylamide (NIPAAm) and 2-methyl-2-oxazoline (MM) macromonomers initiated by 2,2'-azobisisobutyronitrile in dimethylformamide. The macromonomers, with polymerization degrees 31 and 62, were synthesized by r...
Autores: | , |
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Formato: | artículo |
Fecha de Publicación: | 2021 |
Institución: | Sociedad Química del Perú |
Repositorio: | Revista de la Sociedad Química del Perú |
Lenguaje: | español |
OAI Identifier: | oai:rsqp.revistas.sqperu.org.pe:article/336 |
Enlace del recurso: | http://revistas.sqperu.org.pe/index.php/revistasqperu/article/view/336 |
Nivel de acceso: | acceso abierto |
Materia: | Graft copolymers NIPAAm thermoresponsive macromonomer polyoxazolines Copolímero de injerto termosensibilidad macromonómero polioxazolinas |
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Revista de la Sociedad Química del Perú |
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dc.title.none.fl_str_mv |
SYNTHESIS AND CHARACTERIZATION OF NEW THERMOSENSITIVE GRAFT COPOLYMERS FROM N-ISOPROPYLACRYLAMIDE AND 2-METHYL-2-OXAZOLINE MACROMONOMERS SÍNTESIS Y CARACTERIZACIÓN DE NUEVOS COPOLÍMEROS DE INJERTO TERMOSENSIBLES A PARTIR DE N-ISOPROPILACRILAMIDA Y MACROMONÓMEROS DE 2-METIL-2-OXAZOLINA |
title |
SYNTHESIS AND CHARACTERIZATION OF NEW THERMOSENSITIVE GRAFT COPOLYMERS FROM N-ISOPROPYLACRYLAMIDE AND 2-METHYL-2-OXAZOLINE MACROMONOMERS |
spellingShingle |
SYNTHESIS AND CHARACTERIZATION OF NEW THERMOSENSITIVE GRAFT COPOLYMERS FROM N-ISOPROPYLACRYLAMIDE AND 2-METHYL-2-OXAZOLINE MACROMONOMERS Rueda, Juan Carlos Graft copolymers NIPAAm thermoresponsive macromonomer polyoxazolines Copolímero de injerto NIPAAm termosensibilidad macromonómero polioxazolinas |
title_short |
SYNTHESIS AND CHARACTERIZATION OF NEW THERMOSENSITIVE GRAFT COPOLYMERS FROM N-ISOPROPYLACRYLAMIDE AND 2-METHYL-2-OXAZOLINE MACROMONOMERS |
title_full |
SYNTHESIS AND CHARACTERIZATION OF NEW THERMOSENSITIVE GRAFT COPOLYMERS FROM N-ISOPROPYLACRYLAMIDE AND 2-METHYL-2-OXAZOLINE MACROMONOMERS |
title_fullStr |
SYNTHESIS AND CHARACTERIZATION OF NEW THERMOSENSITIVE GRAFT COPOLYMERS FROM N-ISOPROPYLACRYLAMIDE AND 2-METHYL-2-OXAZOLINE MACROMONOMERS |
title_full_unstemmed |
SYNTHESIS AND CHARACTERIZATION OF NEW THERMOSENSITIVE GRAFT COPOLYMERS FROM N-ISOPROPYLACRYLAMIDE AND 2-METHYL-2-OXAZOLINE MACROMONOMERS |
title_sort |
SYNTHESIS AND CHARACTERIZATION OF NEW THERMOSENSITIVE GRAFT COPOLYMERS FROM N-ISOPROPYLACRYLAMIDE AND 2-METHYL-2-OXAZOLINE MACROMONOMERS |
dc.creator.none.fl_str_mv |
Rueda, Juan Carlos Paola Palacios, Ana María |
author |
Rueda, Juan Carlos |
author_facet |
Rueda, Juan Carlos Paola Palacios, Ana María |
author_role |
author |
author2 |
Paola Palacios, Ana María |
author2_role |
author |
dc.subject.none.fl_str_mv |
Graft copolymers NIPAAm thermoresponsive macromonomer polyoxazolines Copolímero de injerto NIPAAm termosensibilidad macromonómero polioxazolinas |
topic |
Graft copolymers NIPAAm thermoresponsive macromonomer polyoxazolines Copolímero de injerto NIPAAm termosensibilidad macromonómero polioxazolinas |
description |
New graft copolymers were synthesized from the free radical polymerization of N-isopropylacrylamide (NIPAAm) and 2-methyl-2-oxazoline (MM) macromonomers initiated by 2,2'-azobisisobutyronitrile in dimethylformamide. The macromonomers, with polymerization degrees 31 and 62, were synthesized by ring-opening cationic polymerization of 2-methyl-2-oxazoline initiated by chloromethylstyrene in the presence of sodium iodide. The grafted macromonomers and copolymers were characterized by proton nuclear magnetic resonance spectrometry (1H-RMN) and the conformational transition temperature was determined by turbidimetric measurements and 1H-RMN spectroscopy. The NIPAAm / MM molar ratio in the copolymer, determined by 1H-RMN, was higher than in the feed to the reactor due to the higher reactivity of the NIPAAm due to its greater diffusivity in the reacting medium due to its lower molecular weight. The conformational transition temperature (LCST) of the graft copolymers ranged from 33 to 38 °C and the intensity of the same was a function of the molar ratio of NIPAAm / macromonomer within the graft copolymer. The value of the LCST increased, and at the same time its intensity decreased, as the NIPAAm / MM molar ratio decreased in the copolymer. The LCST also decreased even more in intensity as the degree of polymerization of the macromonomer increased. From the LCST temperature, the graft copolymers with a relatively high content of MM could form micelles or molecular aggregates type "core-shell" in aqueous solution, which would be formed by a core with collapsed segments of polyNIPAAm and a shell formed of hydrophilic polymethyloxazoline chains, which partially prevent an intermolecular collapse of these aggregates. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-11-01 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Text texto |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://revistas.sqperu.org.pe/index.php/revistasqperu/article/view/336 10.37761/rsqp.v87i2.336 |
url |
http://revistas.sqperu.org.pe/index.php/revistasqperu/article/view/336 |
identifier_str_mv |
10.37761/rsqp.v87i2.336 |
dc.language.none.fl_str_mv |
spa |
language |
spa |
dc.relation.none.fl_str_mv |
http://revistas.sqperu.org.pe/index.php/revistasqperu/article/view/336/307 |
dc.rights.none.fl_str_mv |
https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.coverage.none.fl_str_mv |
2021 2021 |
dc.publisher.none.fl_str_mv |
Sociedad Química del Perú |
publisher.none.fl_str_mv |
Sociedad Química del Perú |
dc.source.none.fl_str_mv |
Revista de la Sociedad Química del Perú; Vol. 87 Núm. 2 (2021): Revista de la Sociedad Química del Perú; 163-179 Journal of the Chemical Society of Peru; Vol. 87 No. 2 (2021): Journal of Sociedad Química del Perú; 163-179 2309-8740 1810-634X 10.37761/rsqp.v87i2 reponame:Revista de la Sociedad Química del Perú instname:Sociedad Química del Perú instacron:SQP |
instname_str |
Sociedad Química del Perú |
instacron_str |
SQP |
institution |
SQP |
reponame_str |
Revista de la Sociedad Química del Perú |
collection |
Revista de la Sociedad Química del Perú |
repository.name.fl_str_mv |
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repository.mail.fl_str_mv |
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1844704002486304768 |
spelling |
SYNTHESIS AND CHARACTERIZATION OF NEW THERMOSENSITIVE GRAFT COPOLYMERS FROM N-ISOPROPYLACRYLAMIDE AND 2-METHYL-2-OXAZOLINE MACROMONOMERSSÍNTESIS Y CARACTERIZACIÓN DE NUEVOS COPOLÍMEROS DE INJERTO TERMOSENSIBLES A PARTIR DE N-ISOPROPILACRILAMIDA Y MACROMONÓMEROS DE 2-METIL-2-OXAZOLINARueda, Juan CarlosPaola Palacios, Ana MaríaGraft copolymersNIPAAmthermoresponsivemacromonomerpolyoxazolinesCopolímero de injertoNIPAAmtermosensibilidadmacromonómeropolioxazolinasNew graft copolymers were synthesized from the free radical polymerization of N-isopropylacrylamide (NIPAAm) and 2-methyl-2-oxazoline (MM) macromonomers initiated by 2,2'-azobisisobutyronitrile in dimethylformamide. The macromonomers, with polymerization degrees 31 and 62, were synthesized by ring-opening cationic polymerization of 2-methyl-2-oxazoline initiated by chloromethylstyrene in the presence of sodium iodide. The grafted macromonomers and copolymers were characterized by proton nuclear magnetic resonance spectrometry (1H-RMN) and the conformational transition temperature was determined by turbidimetric measurements and 1H-RMN spectroscopy. The NIPAAm / MM molar ratio in the copolymer, determined by 1H-RMN, was higher than in the feed to the reactor due to the higher reactivity of the NIPAAm due to its greater diffusivity in the reacting medium due to its lower molecular weight. The conformational transition temperature (LCST) of the graft copolymers ranged from 33 to 38 °C and the intensity of the same was a function of the molar ratio of NIPAAm / macromonomer within the graft copolymer. The value of the LCST increased, and at the same time its intensity decreased, as the NIPAAm / MM molar ratio decreased in the copolymer. The LCST also decreased even more in intensity as the degree of polymerization of the macromonomer increased. From the LCST temperature, the graft copolymers with a relatively high content of MM could form micelles or molecular aggregates type "core-shell" in aqueous solution, which would be formed by a core with collapsed segments of polyNIPAAm and a shell formed of hydrophilic polymethyloxazoline chains, which partially prevent an intermolecular collapse of these aggregates.Fueron sintetizados nuevos copolímeros injertados a partir de la polimerización por radicales libres de N-isopropilacrilamida (NIPAAm) y macromonómeros de 2-metil-2-oxazolina (MM) iniciada por el 2,2´-azobisisobutironitrilo en dimetilformamida. Los macromonómeros, de grados de polimerización 31 y 62, fueron sintetizados mediante la polimerización catiónica por apertura de anillo de 2-metil-2-oxazolina iniciada por el clorometilestireno en presencia de ioduro de sodio. Los macromonómeros y copolímeros injertados fueron caracterizados por espectrometría de resonancia magnética nuclear de protones (1H-RMN) y la temperatura de transición conformacional fue determinada mediante mediciones turbidimétricas yespectroscopía 1H-RMN.La razón molar NIPAAm/MM en el copolímero, determinada por 1H-RMN, fue mayor que en la alimentación al reactor debido a la mayor reactividad del NIPAAm por su mayor difusividad en el medio reaccionante debido a su menor peso molecular. La temperatura de transición conformacional (LCST) de los copolímeros injertados estuvo en el rango de 33 a 38 °C y la intensidad de la misma fue función de la razón molar de NIPAAm/ macromonómero dentro del copolímero injertado. Se incrementó el valor de la LCST, y al mismo tiempo disminuyó su intensidad, al disminuir la razón molar NIPAAm/MM en el copolímero. La LCST también disminuyó aún más en intensidad al aumentar el grado de polimerización del macromonómero. A partir de la temperatura LCST, los copolímeros injertados con un relativamente alto contenido de MM podrían formar micelas o agregados moleculares tipo “core-shell” en solución acuosa, que estarían formados por un núcleo con segmentos colapsados de poliNIPAAm y una corona formada de cadenas hidrofílicas de polimetiloxazolina, las cuales impiden parcialmente un colapso intermolecular de estos agregados.Sociedad Química del Perú2021-11-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionTexttextoapplication/pdfhttp://revistas.sqperu.org.pe/index.php/revistasqperu/article/view/33610.37761/rsqp.v87i2.336Revista de la Sociedad Química del Perú; Vol. 87 Núm. 2 (2021): Revista de la Sociedad Química del Perú; 163-179Journal of the Chemical Society of Peru; Vol. 87 No. 2 (2021): Journal of Sociedad Química del Perú; 163-1792309-87401810-634X10.37761/rsqp.v87i2reponame:Revista de la Sociedad Química del Perúinstname:Sociedad Química del Perúinstacron:SQPspahttp://revistas.sqperu.org.pe/index.php/revistasqperu/article/view/336/30720212021https://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessoai:rsqp.revistas.sqperu.org.pe:article/3362022-01-13T23:43:34Z |
score |
13.408957 |
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La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).