Sökning: "reaction progress kinetic analysis"
Hittade 4 avhandlingar innehållade orden reaction progress kinetic analysis.
1. Organocatalytic Acylation for the Kinetic Resolution of Secondary Aryl Alcohols : Synthetic Applications and Mechanistic Studies
Sammanfattning : The research described in this thesis focuses on the catalytic acylative kinetic resolution (KR) of aromatic secondary alcohols, using a planar-chiral 4-(dimethylamino)pyridine (DMAP) organocatalyst.In the first part of this thesis, the substrate scope of the above mentioned process was expanded to aromatic secondary alcohols that contain an extra functional group in the alkyl moiety, such as 1,2-azido alcohols, 2-hydroxy-2-aryl-ethylphosphonates and 2-hydroxy-2-aryl esters. LÄS MER
2. Sensitivity, Noise and Detection of Enzyme Inhibition in Progress Curves
Sammanfattning : Starting with the development of an enzymatic assay, where an enzyme in solution hydrolysed a solid-phase bound peptide, a model for the kinetics of enzyme action was introduced. This model allowed the estimation of kinetic parameters and enzyme activity for a system that has the peculiarity of not being saturable with the substrate, but with the enzyme. LÄS MER
3. Investigations of the Kinetics of Reduction and Reduction/Carburization of NiO-WO3 Precursors
Sammanfattning : Kinetic studies of reduction of the mixtures of NiO and WO3 having different Ni/(Ni+W) molar ratios in flowing hydrogen gas were investigated by means of Thermo Gravimetric Analysis (TGA), Fluidized Bed (FB) technique as well as Thermal diffusivity measurements under isothermal conditions. In the case of TGA, the reaction progress was monitored by mass loss, while evolved gas analysis by a gas chromatograph was the indicator of the reaction progress in the case of FB. LÄS MER
4. Development of an efficient solver for detailed kinetics in reactive flows
Sammanfattning : The use of chemical kinetic mechanisms in CAE tools for reactive flow simulations is of high importance for studying and predicting pollutant formation. However, usage of complex reaction schemes is accompanied by high computational cost in both 1D and 3D-CFD frameworks. LÄS MER