Continuous hydroformylation of 1-decene ...
Type de document :
Article dans une revue scientifique: Article original
DOI :
URL permanente :
Titre :
Continuous hydroformylation of 1-decene in an aqueous biphasic system enabled by methylated cyclodextrins
Auteur(s) :
Kuenneman, n K. U. [Auteur]
Schurm, L. [Auteur]
Lange, D. [Auteur]
Seidensticker, T. [Auteur]
Tilloy, Sebastien [Auteur]
UCCS Équipe Catalyse Supramoléculaire
Monflier, Eric [Auteur]
UCCS Équipe Catalyse Supramoléculaire
Vogt, D. [Auteur]
Dreimann, J. M. [Auteur]
Schurm, L. [Auteur]
Lange, D. [Auteur]
Seidensticker, T. [Auteur]
Tilloy, Sebastien [Auteur]

UCCS Équipe Catalyse Supramoléculaire
Monflier, Eric [Auteur]

UCCS Équipe Catalyse Supramoléculaire
Vogt, D. [Auteur]
Dreimann, J. M. [Auteur]
Titre de la revue :
Green chemistry . an international journal and green chemistry resource . GC
Nom court de la revue :
Green Chem.
Numéro :
22
Pagination :
3809-3819
Date de publication :
2020-06-21
ISSN :
1463-9262
Discipline(s) HAL :
Chimie/Catalyse
Résumé en anglais : [en]
For the first time, randomly methylated β-cyclodextrin was applied as the mass transfer agent in a continuous process. Considering the example of the Rh-catalyzed hydroformylation of 1-decene, process development was shown, ...
Lire la suite >For the first time, randomly methylated β-cyclodextrin was applied as the mass transfer agent in a continuous process. Considering the example of the Rh-catalyzed hydroformylation of 1-decene, process development was shown, where cyclodextrin was used together with a catalyst system that was continuously recovered and recycled using an aqueous biphasic system. In initial experiments, water-soluble and commercially available Rh/TPPTS and Rh/sulfoxantphos catalyst systems were scaled up from 50 ml into 1000 ml high-pressure autoclave systems to demonstrate their scalability. Both these systems were compared, and they afforded excellent chemoselectivity (>99%) toward the desired linear aldehyde product. In particular, higher regioselectivity (up to 31) was achieved for the Rh/sulfoxantphos system. Investigations regarding the long-term stability of the mass transfer agent and both catalyst systems were carried out in a continuously operated miniplant process. It was shown that the process could be successfully operated under the steady state for over 200 h with chemoselectivity of >97% toward the desired aldehyde product. Simultaneously, extremely low Rh leaching (total: 0.59%) was observed over the entire period of 200 h.Lire moins >
Lire la suite >For the first time, randomly methylated β-cyclodextrin was applied as the mass transfer agent in a continuous process. Considering the example of the Rh-catalyzed hydroformylation of 1-decene, process development was shown, where cyclodextrin was used together with a catalyst system that was continuously recovered and recycled using an aqueous biphasic system. In initial experiments, water-soluble and commercially available Rh/TPPTS and Rh/sulfoxantphos catalyst systems were scaled up from 50 ml into 1000 ml high-pressure autoclave systems to demonstrate their scalability. Both these systems were compared, and they afforded excellent chemoselectivity (>99%) toward the desired linear aldehyde product. In particular, higher regioselectivity (up to 31) was achieved for the Rh/sulfoxantphos system. Investigations regarding the long-term stability of the mass transfer agent and both catalyst systems were carried out in a continuously operated miniplant process. It was shown that the process could be successfully operated under the steady state for over 200 h with chemoselectivity of >97% toward the desired aldehyde product. Simultaneously, extremely low Rh leaching (total: 0.59%) was observed over the entire period of 200 h.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
CNRS
Centrale Lille
ENSCL
Univ. Artois
Université de Lille
Centrale Lille
ENSCL
Univ. Artois
Université de Lille
Collections :
Équipe(s) de recherche :
Catalyse et chimie supramoléculaire (CASU)
Date de dépôt :
2022-03-02T07:13:19Z
2023-12-15T19:46:27Z
2023-12-15T19:51:14Z
2023-12-15T19:46:27Z
2023-12-15T19:51:14Z
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