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A similarity solution is presented for the convective-diffusion equation governing the steady-state concentration polarization boundary layer in crossflow microfiltration of the particles, under conditions where a thin stagnant layer of particles deposited on the microporous membrane surface provides the controlling resistance to filtration.
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The perfluorinated end groups of the nano-hybrid membrane surface provided low energy surface.
More broadly, this work suggests that bulky ligands could be used to drive the accumulation of specific receptors at the plasma membrane surface, providing a biophysical tool for targeted modulation of signaling and metabolism from outside the cell.
The irregularities in the membrane surface provide deep crypts, which act as binding sites for albumin when the circuit is primed with albumin solution.
The interaction of proteins with membrane surfaces provides an example of how different combinations of hydrophobic and electrostatic interactions are combined to achieve various specificities.
The stack is made up of many cell pairs, each cell pair consisting of alternating anion and cation exchange membranes separated by spacer-filled channels which allow fluid to flow across the membrane surfaces, provide mechanical support and maintain intermembrane distance.
We postulate that the positive charge provided by adsorption of QA+ at the membrane's surface provides a constant positive charge density, dependent on the QAS surface activity and concentration.
The model gives an adequate description of membrane surface morphology and provides guidance for the synthesis of zeolite membranes with engineered microstructure.
The results point to a proof for the concept and further indicate that reasonable numbers of fibers and membrane surface area can provide cooling effectiveness comparable to conventional evaporative cooling equipment.
The use of patterned, static surfaces provides new models to design complex membrane topographies and curvatures.
Activated platelets accelerate the coagulation process by providing the membrane surface necessary for the generation of the active form of thrombin, which acts as a potent platelet agonist (for review, see [3]).
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