[article]
Titre : |
Synthesis of dipentyl carbonate by transesterification using basic ionic liquid [bmIm] OH catalyst |
Type de document : |
texte imprimé |
Auteurs : |
Sheng Han, Auteur ; Ming Luo, Auteur ; Xiaoli Zhou, Auteur |
Année de publication : |
2012 |
Article en page(s) : |
pp. 5433–5437 |
Note générale : |
Industrial chemistry |
Langues : |
Anglais (eng) |
Mots-clés : |
catalytic Ionic liquid |
Résumé : |
The catalytic synthesis from transesterification of dimethyl carbonate (DMC) and 1-pentanol (1-PeOH) over alkaline ionic liquid 1-butyl-3-methylimidazolium hydroxide ([bmIm]OH), as well as the optimal reaction conditions, was studied. Results showed that [bmIm]OH exhibited high activity and when the reaction time was 4 h, catalyst dosage was 2.0%, n(DMC):n(1-PeOH) was 1:4, and the dipentyl carbonate (DPC) yield was up to 75.81%. After the alkaline ionic liquid [bmIm]OH was used 5 times repeatedly, the catalytic activity still remained at 94%. |
ISSN : |
0888-5885 |
En ligne : |
http://pubs.acs.org/doi/abs/10.1021/ie202628m |
in Industrial & engineering chemistry research > Vol. 51 N° 15 (Avril 2012) . - pp. 5433–5437
[article] Synthesis of dipentyl carbonate by transesterification using basic ionic liquid [bmIm] OH catalyst [texte imprimé] / Sheng Han, Auteur ; Ming Luo, Auteur ; Xiaoli Zhou, Auteur . - 2012 . - pp. 5433–5437. Industrial chemistry Langues : Anglais ( eng) in Industrial & engineering chemistry research > Vol. 51 N° 15 (Avril 2012) . - pp. 5433–5437
Mots-clés : |
catalytic Ionic liquid |
Résumé : |
The catalytic synthesis from transesterification of dimethyl carbonate (DMC) and 1-pentanol (1-PeOH) over alkaline ionic liquid 1-butyl-3-methylimidazolium hydroxide ([bmIm]OH), as well as the optimal reaction conditions, was studied. Results showed that [bmIm]OH exhibited high activity and when the reaction time was 4 h, catalyst dosage was 2.0%, n(DMC):n(1-PeOH) was 1:4, and the dipentyl carbonate (DPC) yield was up to 75.81%. After the alkaline ionic liquid [bmIm]OH was used 5 times repeatedly, the catalytic activity still remained at 94%. |
ISSN : |
0888-5885 |
En ligne : |
http://pubs.acs.org/doi/abs/10.1021/ie202628m |
|