Porous membranes having amphoteric charge groups were prepared by heterogeneous graft polymerization
from aqueous solution containing acrylic acid and (N,N-dimethylamino)propyl acrylamide. The charging
properties of the amphoteric charge groups grafted to the pore surface were investigated by ζ potentials
obtained from streaming potential measurements. Theoretical development in terms of the amphoteric
pore surface was attempted by introducing a site dissociation model of pH-dependent ζ potentials. The
theoretical model is based on the assumption that the surface charge arises only from the protonation and
deprotonation of the charged surface groups exposed to electrolyte solution. Good fits between experimental
results and theoretical equations were attained, and thereby the isoelectric point, dissociation constant,
apparent surface site density, and acid-to-base ratio of the amphoteric pore surface were determined.
Depending on the variation in the feed monomer ratio for graft polymerization, these parameters
correspondingly changed. If we assumed that the acid-to-base ratio of the amphoteric pore surface
corresponds to that in the whole membrane, the net charge density of the membrane quantitatively obtained
from the potentiometric titration gave the respective charge densities of acidic and basic groups using the
acid-to-base ratio determined from the site dissociation model. Here we proposed an approach to characterize
the amphoteric-charged pore surface by the pH-dependent ζ potential and its theoretical modeling.