Curing and thermal behavior of epoxy resins of hexafluoro - bisphenol –A and bisphenol-A
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Polímeros (São Carlos. Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-14282016000100003 |
Resumo: | Abstract This paper describes the synthesis and characterization of epoxy resins based on (hexafluoroisopropylidene)diphenol (EFN) and p,p’-isopropylidenebisphenol (EBN), respectively and 4, 4’- (hexafluoroisopropylidene)dipthalic-imideamine (IMAM), a curing agent. The synthesized epoxy resins and IMAM curing agent were characterized by Fourier Transform Infrared (FTIR) and 1H Nuclear Magnetic Resonance (NMR) spectroscopy.13C NMR technique was also used to characterize IMAM. Study of curing behavior of EFN and EBN with stoichiometric amount of aromatic 4,4’-diaminodiphenylmethane (DDM), 4,4’-diaminodiphenylsulfone (DDS) and IMAM by using Differential Scanning Calorimetery (DSC) indicated that IMAM was least reactive curing agent towards both epoxy resins as compared to DDS and DDM. The investigation of thermal decomposition of the cured compounds by thermogravimetric analyzer (TGA) indicated the higher thermal stability of EFN and EBN resins initially with DDS and at elevated temperatures with IMAM. It was also observed that EFN resins were thermally more stable than EBN resins cured with corresponding curing agents. |
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Curing and thermal behavior of epoxy resins of hexafluoro - bisphenol –A and bisphenol-Aaromatic diaminescuring behaviorepoxy resinsimide aminethermal propertiesAbstract This paper describes the synthesis and characterization of epoxy resins based on (hexafluoroisopropylidene)diphenol (EFN) and p,p’-isopropylidenebisphenol (EBN), respectively and 4, 4’- (hexafluoroisopropylidene)dipthalic-imideamine (IMAM), a curing agent. The synthesized epoxy resins and IMAM curing agent were characterized by Fourier Transform Infrared (FTIR) and 1H Nuclear Magnetic Resonance (NMR) spectroscopy.13C NMR technique was also used to characterize IMAM. Study of curing behavior of EFN and EBN with stoichiometric amount of aromatic 4,4’-diaminodiphenylmethane (DDM), 4,4’-diaminodiphenylsulfone (DDS) and IMAM by using Differential Scanning Calorimetery (DSC) indicated that IMAM was least reactive curing agent towards both epoxy resins as compared to DDS and DDM. The investigation of thermal decomposition of the cured compounds by thermogravimetric analyzer (TGA) indicated the higher thermal stability of EFN and EBN resins initially with DDS and at elevated temperatures with IMAM. It was also observed that EFN resins were thermally more stable than EBN resins cured with corresponding curing agents.Associação Brasileira de Polímeros2016-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-14282016000100003Polímeros v.26 n.1 2016reponame:Polímeros (São Carlos. Online)instname:Associação Brasileira de Polímeros (ABPol)instacron:ABPO10.1590/0104-1428.2041info:eu-repo/semantics/openAccessKiran,VaishnavGaur,Bhartieng2016-12-16T00:00:00Zoai:scielo:S0104-14282016000100003Revistahttp://www.scielo.br/pohttps://old.scielo.br/oai/scielo-oai.php||revista@abpol.org.br1678-51690104-1428opendoar:2016-12-16T00:00Polímeros (São Carlos. Online) - Associação Brasileira de Polímeros (ABPol)false |
dc.title.none.fl_str_mv |
Curing and thermal behavior of epoxy resins of hexafluoro - bisphenol –A and bisphenol-A |
title |
Curing and thermal behavior of epoxy resins of hexafluoro - bisphenol –A and bisphenol-A |
spellingShingle |
Curing and thermal behavior of epoxy resins of hexafluoro - bisphenol –A and bisphenol-A Kiran,Vaishnav aromatic diamines curing behavior epoxy resins imide amine thermal properties |
title_short |
Curing and thermal behavior of epoxy resins of hexafluoro - bisphenol –A and bisphenol-A |
title_full |
Curing and thermal behavior of epoxy resins of hexafluoro - bisphenol –A and bisphenol-A |
title_fullStr |
Curing and thermal behavior of epoxy resins of hexafluoro - bisphenol –A and bisphenol-A |
title_full_unstemmed |
Curing and thermal behavior of epoxy resins of hexafluoro - bisphenol –A and bisphenol-A |
title_sort |
Curing and thermal behavior of epoxy resins of hexafluoro - bisphenol –A and bisphenol-A |
author |
Kiran,Vaishnav |
author_facet |
Kiran,Vaishnav Gaur,Bharti |
author_role |
author |
author2 |
Gaur,Bharti |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Kiran,Vaishnav Gaur,Bharti |
dc.subject.por.fl_str_mv |
aromatic diamines curing behavior epoxy resins imide amine thermal properties |
topic |
aromatic diamines curing behavior epoxy resins imide amine thermal properties |
description |
Abstract This paper describes the synthesis and characterization of epoxy resins based on (hexafluoroisopropylidene)diphenol (EFN) and p,p’-isopropylidenebisphenol (EBN), respectively and 4, 4’- (hexafluoroisopropylidene)dipthalic-imideamine (IMAM), a curing agent. The synthesized epoxy resins and IMAM curing agent were characterized by Fourier Transform Infrared (FTIR) and 1H Nuclear Magnetic Resonance (NMR) spectroscopy.13C NMR technique was also used to characterize IMAM. Study of curing behavior of EFN and EBN with stoichiometric amount of aromatic 4,4’-diaminodiphenylmethane (DDM), 4,4’-diaminodiphenylsulfone (DDS) and IMAM by using Differential Scanning Calorimetery (DSC) indicated that IMAM was least reactive curing agent towards both epoxy resins as compared to DDS and DDM. The investigation of thermal decomposition of the cured compounds by thermogravimetric analyzer (TGA) indicated the higher thermal stability of EFN and EBN resins initially with DDS and at elevated temperatures with IMAM. It was also observed that EFN resins were thermally more stable than EBN resins cured with corresponding curing agents. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-03-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-14282016000100003 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-14282016000100003 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/0104-1428.2041 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Associação Brasileira de Polímeros |
publisher.none.fl_str_mv |
Associação Brasileira de Polímeros |
dc.source.none.fl_str_mv |
Polímeros v.26 n.1 2016 reponame:Polímeros (São Carlos. Online) instname:Associação Brasileira de Polímeros (ABPol) instacron:ABPO |
instname_str |
Associação Brasileira de Polímeros (ABPol) |
instacron_str |
ABPO |
institution |
ABPO |
reponame_str |
Polímeros (São Carlos. Online) |
collection |
Polímeros (São Carlos. Online) |
repository.name.fl_str_mv |
Polímeros (São Carlos. Online) - Associação Brasileira de Polímeros (ABPol) |
repository.mail.fl_str_mv |
||revista@abpol.org.br |
_version_ |
1754212589598932992 |