1 |
Amino-acid derived hydroxamic acids as ligands in asymmetric vanadium catalysed epoxidationBourhani, Zaïnaba January 2005 (has links)
No description available.
|
2 |
Intramolecular cyclopropanation of unsaturated terminal epoxides and chlorohydrinsChung, Ying Kit January 2006 (has links)
No description available.
|
3 |
Borrowing hydrogen : a novel concept for C-C bond formation with alcoholsEdwards, Michael Gareth January 2003 (has links)
No description available.
|
4 |
A new route to polyhydric alcoholsParker, Gemma M. January 2009 (has links)
Pentaerythritol is an important industrial chemical for use in paints and coatings, primarily, but also in fuels, explosives, medicine and polymers. The current process for this material is over 50 years old and is a multi-step process involving 3 homogeneous aldolizations and a crossed Cannizzaro reaction, generating 1.5 tonnes of waste for every 4 tonnes of product. This is also very energy inefficient. We are currently developing a radically different concept, shown below. This will deliver an integrated heterogeneous catalytic process with no waste and a high energy and materials efficiency. Methanol/ Dehydrogenation Base Hydrog Ethanol Catalyst Catalyst Catalyst Pentaerythritol The initial step, CH3OH HCHO + H2, will involve the use of Ag/SiO2 catalysts. This will be in the absence of O2, which differs from the current oxidative dehydrogenation process used to produce HCHO, i.e. a direct dehydrogenation. This step has been optimised by investigation of different surface properties to determine how surface area and dispersion will affect the overall adsorption and consequently the methanol/ethanol conversion and product yields. Deactivation of these catalysts has also been touched on by use of in-situ temperature programmed oxidation’s. Base catalysis involving an aldol type reaction of 2 aldehydes, HCHO and CH3CHO, will give the methylolated aldehyde intermediate. This will then undergo a final hydrogenation to the desired product. Any unreacted aldehydes will, therefore, be hydrogenated back to starting materials and consequently recycled. It will be attempted to couple all three reactions to explore how the catalysts perform when used in succession.
|
Page generated in 0.0126 seconds