Kontinuierliche Reaktionsführung mit löslichen Enzymen

Continuous processes with soluble enzymes. This paper surveys the use of continuously operating enzyme-membrane reactors with enforced flow where the retention of soluble enzymes in the reaction vessel is achieved by means of an ultrafiltration membrane. This technique has been commercialized in the acylase process for the synthesis of L -amino acids on a 200 ton/year level. It is especially useful for the application of multi-enzyme systems with cofactor regeneration. The synthesis of L -tert-leucine from the corresponding α-keto acid has been achieved on a kilogram scale. Coenzymes coupled to water soluble polymers are retained in the membrane-reactor together with the enzymes. Use of suitable conditions prevents loss of enzyme and coenzyme by passage through the membrane or by deactivation. Therefore the costs of enzymes and coenzymes are no longer limitations for economic processes. In the continuously operating enzyme-membrane reactor regeneration of the coenzyme up to 600 000 times was achieved. In continuous peptide synthesis space-time yields of 25 kg/(l d) were obtained. To suppress side reactions very high catalyst concentrations are possible, yielding residence times below 4 min.     

Aluminium nitride coatings on silicon carbide fibres,prepared by pyrolysis of a polymeric precursor

Metallic aluminium was anodically dissolved in an organic electrolyte. A viscous solution, containing a polyiminoalane precursor was obtained. Nicalon (SiC) fibres were thermally pretreated and then coated with this fluid. The coated fibres were dried and calcined at 900 ° C in anhydrous ammonia. Thermal pretreatment of the fibres in nitrogen at 1400 ° C and dip coating with solutions of relatively low aluminium concentrations resulted in dense, nearly uncracked aluminium nitride layers.     

Bainite in steels

The mechanism of the bainite transformation in steels is reviewed, beginning with a summary of the early research and finishing with an assessment of the transformation in the context of the other reactions which occur as austenite is cooled to temperatures where it is no longer the stable phase. The review includes a detailed account of the microstructure, chemistry, and crystallography of bainitic ferrite and of the variety of carbide precipitation reactions associated with the bainite transformation. This is followed by an assessment of the thermodynamic and kinetic characteristics of the reaction and by a consideration of the reverse transformation from bainite to austenite. It is argued that there are useful mechanistic distinctions to be made between the coherent growth of ferrite initially supersaturated with carbon (bainite), coherent growth of Widmanstätten ferrite under paraequilibrium conditions, and incoherent growth of ferrite under local equilibrium or paraequilibrium conditions. The nature of the so-called acicular ferrite is also discussed.