A chemical platform approach on cardanol oil: from the synthesis of building blocks to polymer synthesis
This review proposes a platform approach for the synthesis of various building blocks from cardanol oil in one or two-steps synthesis. Cardanol is a natural phenol issued from Cashew nutshell liquid (CNSL). CNSL is a non-edible renewable resource, co-produced from cashew industry in large commercial...
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EDP Sciences
2016-09-01
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Series: | Oilseeds and fats, crops and lipids |
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Online Access: | http://dx.doi.org/10.1051/ocl/2016022 |
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doaj-fc8f1c4f65544c749938a3cc46f36c752021-04-02T15:35:17ZengEDP SciencesOilseeds and fats, crops and lipids2272-69772257-66142016-09-01235D51110.1051/ocl/2016022ocl160002A chemical platform approach on cardanol oil: from the synthesis of building blocks to polymer synthesisJaillet FannyDarroman EmilieBoutevin BernardCaillol SylvainThis review proposes a platform approach for the synthesis of various building blocks from cardanol oil in one or two-steps synthesis. Cardanol is a natural phenol issued from Cashew nutshell liquid (CNSL). CNSL is a non-edible renewable resource, co-produced from cashew industry in large commercial volumes. Cardanol is non-toxic and particularly suitable as an aromatic renewable resource for polymers and materials. Various routes were used for the synthesis of di- and poly-functional building blocks used thereafter in polymer syntheses. Phenolation was used to dimerize/oligomerize cardanol to propose increase functionality of cardanol. Thio-ene was used to synthesize new reactive amines. Epoxidation and (meth)acrylation were also used to insert oxirane or (meth)acrylate groups in order to synthesize polymers and materials.http://dx.doi.org/10.1051/ocl/2016022Cardanolepoxideacrylatecarbonateaminevinyl ester |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jaillet Fanny Darroman Emilie Boutevin Bernard Caillol Sylvain |
spellingShingle |
Jaillet Fanny Darroman Emilie Boutevin Bernard Caillol Sylvain A chemical platform approach on cardanol oil: from the synthesis of building blocks to polymer synthesis Oilseeds and fats, crops and lipids Cardanol epoxide acrylate carbonate amine vinyl ester |
author_facet |
Jaillet Fanny Darroman Emilie Boutevin Bernard Caillol Sylvain |
author_sort |
Jaillet Fanny |
title |
A chemical platform approach on cardanol oil: from the synthesis of building blocks to polymer synthesis |
title_short |
A chemical platform approach on cardanol oil: from the synthesis of building blocks to polymer synthesis |
title_full |
A chemical platform approach on cardanol oil: from the synthesis of building blocks to polymer synthesis |
title_fullStr |
A chemical platform approach on cardanol oil: from the synthesis of building blocks to polymer synthesis |
title_full_unstemmed |
A chemical platform approach on cardanol oil: from the synthesis of building blocks to polymer synthesis |
title_sort |
chemical platform approach on cardanol oil: from the synthesis of building blocks to polymer synthesis |
publisher |
EDP Sciences |
series |
Oilseeds and fats, crops and lipids |
issn |
2272-6977 2257-6614 |
publishDate |
2016-09-01 |
description |
This review proposes a platform approach for the synthesis of various building blocks from cardanol oil in one or two-steps synthesis. Cardanol is a natural phenol issued from Cashew nutshell liquid (CNSL). CNSL is a non-edible renewable resource, co-produced from cashew industry in large commercial volumes. Cardanol is non-toxic and particularly suitable as an aromatic renewable resource for polymers and materials. Various routes were used for the synthesis of di- and poly-functional building blocks used thereafter in polymer syntheses. Phenolation was used to dimerize/oligomerize cardanol to propose increase functionality of cardanol. Thio-ene was used to synthesize new reactive amines. Epoxidation and (meth)acrylation were also used to insert oxirane or (meth)acrylate groups in order to synthesize polymers and materials. |
topic |
Cardanol epoxide acrylate carbonate amine vinyl ester |
url |
http://dx.doi.org/10.1051/ocl/2016022 |
work_keys_str_mv |
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1721559734943744000 |