Antioxidant activity of cashew nut shell liquid (CNSL) derivatives on the thermal oxidation of synthetic cis-1,4-polyisoprene

Detalhes bibliográficos
Autor(a) principal: Rodrigues,Francisco Helder A.
Data de Publicação: 2006
Outros Autores: Feitosa,Judith P. A., Ricardo,Nágila M. P. S., França,Francisco Célio F. de, Carioca,José Oswaldo B.
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=S0103-50532006000200008
Resumo: CNSL is a mixture of meta-alkylphenols with variable degree of unsaturation attached to the benzene ring. The kinetic study of the thermal degradation at 140 °C of synthetic cis-1,4-polyisoprene film, in the presence of technical CNSL and some derivatives (cardanol, hydrogenated cardanol and alkylated hydrogenated cardanol) was carried out by FTIR. The amount of OH/OOH and C=O formed and also of C=C consumed during the degradation was determined. All materials increase the induction period and decrease the apparent rate constants of thermal-oxidation. Based on kinetic parameters, the order of antioxidant activity was: CNSL >> cardanol <FONT FACE=Symbol>@</FONT> hydrogenated and alkylated cardanol > hydrogenated cardanol. The effect of CNSL could be attributed to the extra contribution of the other components besides cardanol and to the unsaturation on the long side chain. This greater activity is important because CNSL is much more cost effective than its derivatives.
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spelling Antioxidant activity of cashew nut shell liquid (CNSL) derivatives on the thermal oxidation of synthetic cis-1,4-polyisopreneCNSLphenolpolyisoprenethermal oxidationantioxidantCNSL is a mixture of meta-alkylphenols with variable degree of unsaturation attached to the benzene ring. The kinetic study of the thermal degradation at 140 °C of synthetic cis-1,4-polyisoprene film, in the presence of technical CNSL and some derivatives (cardanol, hydrogenated cardanol and alkylated hydrogenated cardanol) was carried out by FTIR. The amount of OH/OOH and C=O formed and also of C=C consumed during the degradation was determined. All materials increase the induction period and decrease the apparent rate constants of thermal-oxidation. Based on kinetic parameters, the order of antioxidant activity was: CNSL >> cardanol <FONT FACE=Symbol>@</FONT> hydrogenated and alkylated cardanol > hydrogenated cardanol. The effect of CNSL could be attributed to the extra contribution of the other components besides cardanol and to the unsaturation on the long side chain. This greater activity is important because CNSL is much more cost effective than its derivatives.Sociedade Brasileira de Química2006-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532006000200008Journal of the Brazilian Chemical Society v.17 n.2 2006reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532006000200008info:eu-repo/semantics/openAccessRodrigues,Francisco Helder A.Feitosa,Judith P. A.Ricardo,Nágila M. P. S.França,Francisco Célio F. deCarioca,José Oswaldo B.eng2006-04-17T00:00:00Zoai:scielo:S0103-50532006000200008Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2006-04-17T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Antioxidant activity of cashew nut shell liquid (CNSL) derivatives on the thermal oxidation of synthetic cis-1,4-polyisoprene
title Antioxidant activity of cashew nut shell liquid (CNSL) derivatives on the thermal oxidation of synthetic cis-1,4-polyisoprene
spellingShingle Antioxidant activity of cashew nut shell liquid (CNSL) derivatives on the thermal oxidation of synthetic cis-1,4-polyisoprene
Rodrigues,Francisco Helder A.
CNSL
phenol
polyisoprene
thermal oxidation
antioxidant
title_short Antioxidant activity of cashew nut shell liquid (CNSL) derivatives on the thermal oxidation of synthetic cis-1,4-polyisoprene
title_full Antioxidant activity of cashew nut shell liquid (CNSL) derivatives on the thermal oxidation of synthetic cis-1,4-polyisoprene
title_fullStr Antioxidant activity of cashew nut shell liquid (CNSL) derivatives on the thermal oxidation of synthetic cis-1,4-polyisoprene
title_full_unstemmed Antioxidant activity of cashew nut shell liquid (CNSL) derivatives on the thermal oxidation of synthetic cis-1,4-polyisoprene
title_sort Antioxidant activity of cashew nut shell liquid (CNSL) derivatives on the thermal oxidation of synthetic cis-1,4-polyisoprene
author Rodrigues,Francisco Helder A.
author_facet Rodrigues,Francisco Helder A.
Feitosa,Judith P. A.
Ricardo,Nágila M. P. S.
França,Francisco Célio F. de
Carioca,José Oswaldo B.
author_role author
author2 Feitosa,Judith P. A.
Ricardo,Nágila M. P. S.
França,Francisco Célio F. de
Carioca,José Oswaldo B.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Rodrigues,Francisco Helder A.
Feitosa,Judith P. A.
Ricardo,Nágila M. P. S.
França,Francisco Célio F. de
Carioca,José Oswaldo B.
dc.subject.por.fl_str_mv CNSL
phenol
polyisoprene
thermal oxidation
antioxidant
topic CNSL
phenol
polyisoprene
thermal oxidation
antioxidant
description CNSL is a mixture of meta-alkylphenols with variable degree of unsaturation attached to the benzene ring. The kinetic study of the thermal degradation at 140 °C of synthetic cis-1,4-polyisoprene film, in the presence of technical CNSL and some derivatives (cardanol, hydrogenated cardanol and alkylated hydrogenated cardanol) was carried out by FTIR. The amount of OH/OOH and C=O formed and also of C=C consumed during the degradation was determined. All materials increase the induction period and decrease the apparent rate constants of thermal-oxidation. Based on kinetic parameters, the order of antioxidant activity was: CNSL >> cardanol <FONT FACE=Symbol>@</FONT> hydrogenated and alkylated cardanol > hydrogenated cardanol. The effect of CNSL could be attributed to the extra contribution of the other components besides cardanol and to the unsaturation on the long side chain. This greater activity is important because CNSL is much more cost effective than its derivatives.
publishDate 2006
dc.date.none.fl_str_mv 2006-04-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532006000200008
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532006000200008
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532006000200008
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.17 n.2 2006
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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