Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Bart Hamers"'
Autor:
Robert Franke, Gerhard Schembecker, Stefan Sievers, Marc Becker, F. Stenger, Christian Bramsiepe, Markus Priske, Bart Hamers, Johannes Martin Elischewski, Tim Seifert
Publikováno v:
Chemical Engineering and Processing: Process Intensification. 95:124-134
Reduction of investment risk is a major challenge in chemical process design. To minimize financial risks a paradigm shift is necessary. Therefore, risk analysis will have to gain importance already during process development. Only in this way can pl
Autor:
F. Stenger, Bart Hamers, Stefan Sievers, Markus Priske, Robert Franke, Marc Becker, Gerhard Schembecker, Phanuel Fakner, Christian Bramsiepe, Tim Seifert
Publikováno v:
Chemical Engineering and Processing: Process Intensification. 85:1-9
One of the future challenges for chemical engineering is the design of flexible plants allowing an adaptation of production output to market development. Consequently, the target for the design of new processes must be the identification of equipment
Autor:
Robert Franke, Sabriye Güven, Marc Becker, Markus Priske, Bart Hamers, Dieter Vogt, Marko M. L. Nieuwenhuizen
Publikováno v:
ChemCatChem. 6:603-610
The kinetics of Rh-catalyzed neohexene hydroformylation were investigated with the bulky monodentate ligand tris(2,4-di-tert-butylphenyl)phosphite. The hydrogenolysis of the Rh–acyl intermediate was identified as the rate-limiting step for both the
Publikováno v:
Catal. Sci. Technol.. 4:524-530
The kinetics of Rh-catalysed cyclooctene hydroformylation were investigated, based on the mechanism described for a single tris(2,4-di-tert-butylphenyl)phosphite ligand coordinated to a rhodium center. The rate limiting step was found to be the coord
Autor:
Dieter Vogt, Dieter Hess, Bart Hamers, Andrea Christiansen, Laura Bini, Robert Franke, Christian Müller, Michèle Janssen
Publikováno v:
Tetrahedron Letters, 51(15), 1971-1975. Elsevier
A new class of diphosphites is described, based on a tetraphenol backbone. Ligands TP1–TP5 were synthesized and fully characterized and their application in the hydroformylation of octenes was investigated. Ligand TP3, bearing a 1-naphthoxy substit
Publikováno v:
ChemCatChem, 1(1), 103-106. Wiley-VCH Verlag
Hydroaminomethylation of 1-octene and piperidine has been carried out using a pyrrole-substituted phosphine ligand (see Scheme; L), giving extremely high activities (TOF6200 h-1) and selectivities (linear/branched ratios>200). Acidic alcohols in the
This paper shows a model-based design method of an integrated reaction and membrane separation process applied to the ligand-assisted hydroformylation of cyclooctene to cyclooctanecarbaldehyde. In order to demonstrate the economic potential of the ap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce893df5eeb184ba387e25d49b890f73
https://doi.org/10.1016/b978-0-444-59520-1.50004-x
https://doi.org/10.1016/b978-0-444-59520-1.50004-x
Autor:
Laura Bini, Christian Mueller, Robert Franke, Dieter Vogt, Dieter Hess, Bart Hamers, Andrea Christiansen, Michèle Janssen
Publikováno v:
ChemInform. 41
Publikováno v:
Advanced Synthesis & Catalysis, 350(2), 332-342. Wiley-VCH Verlag
Hydroaminomethylation reactions were pertormed successtully in an imidazolium-based ionic liquid using a rhodium/sulfoxantphos system by reacting piperidine with different n-alkenes, affording yields higher than 95% of the resulting amine with turnov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7aefe012c6c61f206b92060b5b0f32a6
https://research.tue.nl/nl/publications/5d0248a9-8255-4e1e-bd90-e87bcb249de1
https://research.tue.nl/nl/publications/5d0248a9-8255-4e1e-bd90-e87bcb249de1
Publikováno v:
Artificial Neural Networks — ICANN 2002 ISBN: 9783540440741
ICANN
ICANN
In this paper we investigate the use of compactly supported RBF kernels for nonlinear function estimation with LS-SVMs. The choice of compact kernels, recently proposed by Genton, may lead to computational improvements and memory reduction. Examples,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5cf0991fcace163e66684c53380f515a
https://doi.org/10.1007/3-540-46084-5_117
https://doi.org/10.1007/3-540-46084-5_117