Green and Efficient Modification of Grape Seed Oil to Synthesize Renewable Monomers
Autor(a) principal: | |
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Data de Publicação: | 2021 |
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=S0103-50532021001102120 |
Resumo: | Grape seed is a waste product from the wine and juice industries. However, vegetable oil can be extracted from it, which is a renewable chemical with a huge potential application after chemical modifications, such as epoxidation and maleinization processes. This paper therefore deals with the use of grape seed oil, to produce its epoxidized and maleinized derivatives. Both derivatives were synthesized in order to improve the conversion (99.4%), yield (98.9%) and selectivity (99.5%) values, as well as to decrease the reaction time (3 h) using cleaner energy sources and heterogeneous catalysts, which can be used 4× without regeneration and obtaining similar conversion and yield values, and at least 5× keeping high selectivity. Based on the characterization results, both grape seed oil derivatives may be applied in different fields, including polymer chemistry as a monomer, coating, and paint. In addition, they can be an option to industries that use petrochemical derivatives as precursors. |
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Green and Efficient Modification of Grape Seed Oil to Synthesize Renewable Monomersrenewable chemicalsmaleinization reactionepoxidized derivativesmicrowave synthesisAmberlite-IR120 reusabilityGrape seed is a waste product from the wine and juice industries. However, vegetable oil can be extracted from it, which is a renewable chemical with a huge potential application after chemical modifications, such as epoxidation and maleinization processes. This paper therefore deals with the use of grape seed oil, to produce its epoxidized and maleinized derivatives. Both derivatives were synthesized in order to improve the conversion (99.4%), yield (98.9%) and selectivity (99.5%) values, as well as to decrease the reaction time (3 h) using cleaner energy sources and heterogeneous catalysts, which can be used 4× without regeneration and obtaining similar conversion and yield values, and at least 5× keeping high selectivity. Based on the characterization results, both grape seed oil derivatives may be applied in different fields, including polymer chemistry as a monomer, coating, and paint. In addition, they can be an option to industries that use petrochemical derivatives as precursors.Sociedade Brasileira de Química2021-11-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532021001102120Journal of the Brazilian Chemical Society v.32 n.11 2021reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.21577/0103-5053.20210104info:eu-repo/semantics/openAccessGaglieri,CarolineAlarcon,Rafael TMoura,Aniele deMagri,RaquelSilva-Filho,Luiz C. daBannach,Gilberteng2021-10-20T00:00:00Zoai:scielo:S0103-50532021001102120Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2021-10-20T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Green and Efficient Modification of Grape Seed Oil to Synthesize Renewable Monomers |
title |
Green and Efficient Modification of Grape Seed Oil to Synthesize Renewable Monomers |
spellingShingle |
Green and Efficient Modification of Grape Seed Oil to Synthesize Renewable Monomers Gaglieri,Caroline renewable chemicals maleinization reaction epoxidized derivatives microwave synthesis Amberlite-IR120 reusability |
title_short |
Green and Efficient Modification of Grape Seed Oil to Synthesize Renewable Monomers |
title_full |
Green and Efficient Modification of Grape Seed Oil to Synthesize Renewable Monomers |
title_fullStr |
Green and Efficient Modification of Grape Seed Oil to Synthesize Renewable Monomers |
title_full_unstemmed |
Green and Efficient Modification of Grape Seed Oil to Synthesize Renewable Monomers |
title_sort |
Green and Efficient Modification of Grape Seed Oil to Synthesize Renewable Monomers |
author |
Gaglieri,Caroline |
author_facet |
Gaglieri,Caroline Alarcon,Rafael T Moura,Aniele de Magri,Raquel Silva-Filho,Luiz C. da Bannach,Gilbert |
author_role |
author |
author2 |
Alarcon,Rafael T Moura,Aniele de Magri,Raquel Silva-Filho,Luiz C. da Bannach,Gilbert |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Gaglieri,Caroline Alarcon,Rafael T Moura,Aniele de Magri,Raquel Silva-Filho,Luiz C. da Bannach,Gilbert |
dc.subject.por.fl_str_mv |
renewable chemicals maleinization reaction epoxidized derivatives microwave synthesis Amberlite-IR120 reusability |
topic |
renewable chemicals maleinization reaction epoxidized derivatives microwave synthesis Amberlite-IR120 reusability |
description |
Grape seed is a waste product from the wine and juice industries. However, vegetable oil can be extracted from it, which is a renewable chemical with a huge potential application after chemical modifications, such as epoxidation and maleinization processes. This paper therefore deals with the use of grape seed oil, to produce its epoxidized and maleinized derivatives. Both derivatives were synthesized in order to improve the conversion (99.4%), yield (98.9%) and selectivity (99.5%) values, as well as to decrease the reaction time (3 h) using cleaner energy sources and heterogeneous catalysts, which can be used 4× without regeneration and obtaining similar conversion and yield values, and at least 5× keeping high selectivity. Based on the characterization results, both grape seed oil derivatives may be applied in different fields, including polymer chemistry as a monomer, coating, and paint. In addition, they can be an option to industries that use petrochemical derivatives as precursors. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-11-01 |
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=S0103-50532021001102120 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532021001102120 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.21577/0103-5053.20210104 |
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.32 n.11 2021 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_ |
1750318184470151168 |