Grafting of tetrahydrophthalic and maleic anhydride onto polyolefins in solution

Detalhes bibliográficos
Autor(a) principal: Campos,Paulo G. S.
Data de Publicação: 2004
Outros Autores: Fantini,Márcia C. A., Petri,Denise F. S.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532004000400015
Resumo: Tetrahydrophthalic (THA) and maleic (MA) anhydrides were grafted onto linear low density polyethylene with comonomer 1-butene and 1-octene (LLDPE) in solution in the presence of benzoyl peroxide (BPO) following experimental designs, where anhydride and BPO concentrations, type of comonomer and reaction time were varied. The formulations were analyzed by Fourier transform infrared spectroscopy (FTIR). In the case of THA modified polyolefins, the time of reaction and the interaction between time of reaction and THA concentration influenced the process, whereas the MA and BPO concentrations influenced the grafting of MA onto polyolefins. THA and MA modified polyolefin samples with similar grafting contents were analized by differential scanning calorimetry (DSC) and X-ray diffraction (XRD). THA and MA functionalized polyolefins presented reduction in the melting temperature of 4.3 °C and 1.4 °C, respectively, comparing with the original polymer. These effects corroborate with the strong reduction in the areas of the diffraction peaks (110) and (200) after the grafting process.
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spelling Grafting of tetrahydrophthalic and maleic anhydride onto polyolefins in solutionpolyethyleneanhydrideexperimental designX-ray diffractiondifferential scanning calorimetryTetrahydrophthalic (THA) and maleic (MA) anhydrides were grafted onto linear low density polyethylene with comonomer 1-butene and 1-octene (LLDPE) in solution in the presence of benzoyl peroxide (BPO) following experimental designs, where anhydride and BPO concentrations, type of comonomer and reaction time were varied. The formulations were analyzed by Fourier transform infrared spectroscopy (FTIR). In the case of THA modified polyolefins, the time of reaction and the interaction between time of reaction and THA concentration influenced the process, whereas the MA and BPO concentrations influenced the grafting of MA onto polyolefins. THA and MA modified polyolefin samples with similar grafting contents were analized by differential scanning calorimetry (DSC) and X-ray diffraction (XRD). THA and MA functionalized polyolefins presented reduction in the melting temperature of 4.3 °C and 1.4 °C, respectively, comparing with the original polymer. These effects corroborate with the strong reduction in the areas of the diffraction peaks (110) and (200) after the grafting process.Sociedade Brasileira de Química2004-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532004000400015Journal of the Brazilian Chemical Society v.15 n.4 2004reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532004000400015info:eu-repo/semantics/openAccessCampos,Paulo G. S.Fantini,Márcia C. A.Petri,Denise F. S.eng2004-09-15T00:00:00Zoai:scielo:S0103-50532004000400015Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2004-09-15T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Grafting of tetrahydrophthalic and maleic anhydride onto polyolefins in solution
title Grafting of tetrahydrophthalic and maleic anhydride onto polyolefins in solution
spellingShingle Grafting of tetrahydrophthalic and maleic anhydride onto polyolefins in solution
Campos,Paulo G. S.
polyethylene
anhydride
experimental design
X-ray diffraction
differential scanning calorimetry
title_short Grafting of tetrahydrophthalic and maleic anhydride onto polyolefins in solution
title_full Grafting of tetrahydrophthalic and maleic anhydride onto polyolefins in solution
title_fullStr Grafting of tetrahydrophthalic and maleic anhydride onto polyolefins in solution
title_full_unstemmed Grafting of tetrahydrophthalic and maleic anhydride onto polyolefins in solution
title_sort Grafting of tetrahydrophthalic and maleic anhydride onto polyolefins in solution
author Campos,Paulo G. S.
author_facet Campos,Paulo G. S.
Fantini,Márcia C. A.
Petri,Denise F. S.
author_role author
author2 Fantini,Márcia C. A.
Petri,Denise F. S.
author2_role author
author
dc.contributor.author.fl_str_mv Campos,Paulo G. S.
Fantini,Márcia C. A.
Petri,Denise F. S.
dc.subject.por.fl_str_mv polyethylene
anhydride
experimental design
X-ray diffraction
differential scanning calorimetry
topic polyethylene
anhydride
experimental design
X-ray diffraction
differential scanning calorimetry
description Tetrahydrophthalic (THA) and maleic (MA) anhydrides were grafted onto linear low density polyethylene with comonomer 1-butene and 1-octene (LLDPE) in solution in the presence of benzoyl peroxide (BPO) following experimental designs, where anhydride and BPO concentrations, type of comonomer and reaction time were varied. The formulations were analyzed by Fourier transform infrared spectroscopy (FTIR). In the case of THA modified polyolefins, the time of reaction and the interaction between time of reaction and THA concentration influenced the process, whereas the MA and BPO concentrations influenced the grafting of MA onto polyolefins. THA and MA modified polyolefin samples with similar grafting contents were analized by differential scanning calorimetry (DSC) and X-ray diffraction (XRD). THA and MA functionalized polyolefins presented reduction in the melting temperature of 4.3 °C and 1.4 °C, respectively, comparing with the original polymer. These effects corroborate with the strong reduction in the areas of the diffraction peaks (110) and (200) after the grafting process.
publishDate 2004
dc.date.none.fl_str_mv 2004-08-01
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=S0103-50532004000400015
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532004000400015
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532004000400015
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 Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.15 n.4 2004
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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