Grafting of tetrahydrophthalic and maleic anhydride onto polyolefins in solution
Autor(a) principal: | |
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Data de Publicação: | 2004 |
Outros Autores: | , |
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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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 |
_version_ |
1750318165766701056 |