dc.contributor.author | Gassama, Abdoulaye | |
dc.contributor.author | Ernenwein, Cédric | |
dc.contributor.author | Youssef, Ali | |
dc.contributor.author | Agach, Mickaël | |
dc.contributor.author | Riguet, Emmanuel | |
dc.contributor.author | Marinkovic, Sinisa | |
dc.contributor.author | Estrine, Boris | |
dc.contributor.author | Hoffmann, Norbert | |
dc.date.accessioned | 2023-03-02T16:42:18Z | |
dc.date.available | 2023-03-02T16:42:18Z | |
dc.date.issued | 2013 | |
dc.identifier.uri | http://rivieresdusud.uasz.sn/xmlui/handle/123456789/1707 | |
dc.description.abstract | Furfural obtained from pentose containing biomass such as hemicelluloses is subjected to photooxygenation. The resulting hydroxyfuranone obtained in high yields undergoes acetalization with fatty
alcohols. Using NaHSO3, surfactants are obtained by addition of a sulfonate group to α,β-unsaturated
carboxyl or carbonyl compounds. Addition occurred either at the CvC double bond (6) or at the aldehyde function (7). Compared to conventional surfactants of this type, the resulting compounds possess
similar good detergent properties. In the case of compound family 6 and when compared to the corresponding alkylsulfate and alkylsulfonate surfactants, even lower critical micelle concentrations (CMC) are
observed. Biodegradation of the new surfactants was determined according to the OECD Test guideline
301 F. Compounds of family 6 are biodegradable. Biodegradation of compounds of family 7 stopped
after 10 days. | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartofseries | The Royal Society of Chemistry;15 : pp. 1558–1566 | |
dc.subject | Furfural | en_US |
dc.subject | Pentose | en_US |
dc.subject | Biomass | en_US |
dc.title | Sulfonated surfactants obtained from furfural | en_US |
dc.type | Article | en_US |
dc.territoire | Région de Ziguinchor | en_US |