David Stuckey
Imperial College London, Chemical Engineering, Faculty Member
Research Interests:
This study seeks to examine the ability of non-ionic/non-polar Colloidial Liquid Aphrons (CLAs) to preserve enzyme functionality upon immobilization and release. CLAs consisting of micron-sized oil droplets surrounded by a thin aqueous... more
This study seeks to examine the ability of non-ionic/non-polar Colloidial Liquid Aphrons (CLAs) to preserve enzyme functionality upon immobilization and release. CLAs consisting of micron-sized oil droplets surrounded by a thin aqueous layer stabilized by a mixture of surfactants, were formulated by direct addition (pre-manufacture addition) using 1% Tween 80/ mineral oil and 1% Tween 20 and the enzymes lipase, aprotinin and α-chymotrypsin. The results of activity assays for both lipase and α-chymotrypsin showed that kinetic activity increased upon immobilization by factors of 7 and 5.5, respectively, while aprotinin retained approximately 85% of its native activity. The conformation of the enzymes released through desorption showed no significant alterations compared to their native state. Changes in pH and temperature showed that optimum conditions did not change after immobilization, while analysis of activation energy for the immobilized enzyme showed an increase in activity at ...
Research Interests:
Research Interests:
Research Interests: Water, Kinetics, Wastewater Treatment, Multidisciplinary, Energy Metabolism, and 19 moreMethane, Fulvic acid, Gel Permeation Chromatography, Enzyme, Biological treatment, Amino Acid Profile, Continuous stirred tank reactor, Chemical Oxygen Demand, Molecular weight, Hydraulic Retention Time, Process Parameters, Granular Activated Carbon, Organic Compound, Biochemical Oxygen Demand, Organic Loading Rate, Anaerobic Baffled Reactor, Product Modelling, Organic Acid, and Nucleic Acid
Research Interests:
ABSTRACT The mass transfer characteristics of a non-porous silicone rubber membrane contacting an aqueous and an organic phase were determined using a shell and tube mass exchanger. Firstly, the stability of the liquid/membrane interfaces... more
ABSTRACT The mass transfer characteristics of a non-porous silicone rubber membrane contacting an aqueous and an organic phase were determined using a shell and tube mass exchanger. Firstly, the stability of the liquid/membrane interfaces was examined, and when positive aqueous phase transmembrane pressure differentials of up to 2 bar were applied, no bulk transmembrane flow of either liquid was observed. This result was not affected by the addition of surfactants or biomass to the aqueous phase, and therefore it seems that phase breakthrough, common with porous membranes, is avoided. Secondly, the mass transfer characteristics of a range of model solutes were investigated and explained with a resistances in series model. A high membrane/aqueous partition coefficient (Pmemaq) (approximately>25) resulted in the aqueous phase film resistance limiting, whilst a low Pmemaq (approximately<5) resulted in the membrane resistance limiting. In contact with organic solvents the silicone rubber swelled to various degrees, and this was solvent dependent. The degree of swelling, and the relative partitioning of the solute into the swelling solvent, impacted on Pmemaq and the membrane diffusion coefficient. These two parameters could be increased by using a highly swelling solvent (solvent constituting>50% of the swollen membrane volume) with a high organic/aqueous partition coefficient (Porgaq) for the solute. In this way the membrane resistance for some solutes was decreased, and therefore the overall mass transfer coefficient increased. Finally, the effect of the presence of other hydrophobic solutes on the rate of mass transfer was investigated, and in the case of geraniol and citronellol (two chemically similar solutes with low water solubilities, 0.7 and 0.35 g l−1, respectively) the effect was similar to a “salting out” phenomena. This resulted in an increase of Porgaq for both geraniol and citronellol, and therefore a decrease in flux of the solute transferring to the aqueous phase.