EFFECT OF INTERPARTICLE ELECTROSTATIC DOUBLE-LAYER INTERACTIONS ON PERMEATE FLUX DECLINE IN CROSS-FLOW MEMBRANE FILTRATION OF COLLOIDAL SUSPENSIONS - AN EXPERIMENTAL INVESTIGATION
Rs. Faibish et al., EFFECT OF INTERPARTICLE ELECTROSTATIC DOUBLE-LAYER INTERACTIONS ON PERMEATE FLUX DECLINE IN CROSS-FLOW MEMBRANE FILTRATION OF COLLOIDAL SUSPENSIONS - AN EXPERIMENTAL INVESTIGATION, Journal of colloid and interface science (Print), 204(1), 1998, pp. 77-86
A systematic study on the effect of electrostatic double layer interac
tion on permeate flux decline and deposit cake formation in crossflow
membrane filtration of colloidal suspensions is reported. Three monodi
sperse silica suspensions with diameters of 47, 110, and 310 nm were u
sed as model colloids, and a tabular zirconia membrane with an average
pore diameter of 20 nm was used as a model membrane. The magnitude an
d range of the electrostatic double layer interactions were controlled
via changes in solution ionic strength and pH. The coupling between c
olloidal interactions and hydrodynamic forces was investigated by chan
ging the transmembrane pressure and particle size. The results indicat
e that the rate of flux decline is strongly dependent on solution ioni
c strength and, to a much lesser degree, on solution pH (for the inves
tigated pH range 6.1-10.0). Variations in flux decline rate with solut
ion ionic strength are especially significant as the particle size dec
reases. Particle cake thickness, permeability, and porosity generally
increased with a decrease in solution ionic strength for a given parti
cle size. For given physical and chemical conditions, the cake layer p
orosity increased with decreasing particle size, while cake permeabili
ty decreased with decreasing particle size. These trends are consisten
t with the increased importance of double layer repulsive forces in co
ntrolling the cake layer structure as the solution ionic strength and
particle size decrease. Pressure relaxation experiments indicated that
the particle cake layer is reversible, implying no irreversible depos
ition (attachment) of silica colloids onto the zirconia membrane surfa
ce. (C) 1998 Academic Press.