Jy. Ho et al., The effect of fluorinated surface modifying macromolecules on the surface morphology of polyethersulfone membranes, J BIOM SC P, 11(10), 2000, pp. 1085-1104
Polyethersulfone (PES) has been recently adopted for membrane materials in
applications such as ultrafiltration and haemodialysis. As a biomaterial, t
he factors which affect the blood compatibility of PES membranes include su
rface energetics, hydrophobicity, and surface morphology. Surface fluorinat
ion of materials has been found to create surfaces with improved blood comp
atibility and chemical stability. One never approach to generating fluorina
ted polymer surfaces has included the use of fluorinated surface modifying
macromolecules (SMMs). These macromolecules have been reported to establish
fluorinated functional groups at surfaces of polymeric materials without s
ignificantly affecting the physical properties of the base polymer. However
, to date there has been relatively little information published on the nat
ure of the surface structure for PES materials containing these SMMs. In th
is study, synthesized SMMs with varying chemical compositions were characte
rized and blended with PES, and fabricated into flat sheet membranes. The b
ulk thermal transitions of PES materials were not significantly altered by
the addition of 4 wt% SMMs. Contact angle data showed that the addition of
SMMs in PES created more hydrophobic surfaces, accompanied by an increase i
n surface heterogeneity. X-ray photoelectron spectroscopy studies confirmed
the presence of elemental fluorine at the surface. Through microscopy stud
ies, it was shown that surface modification was achieved by the migration o
f SMM concentrated microdomains to the air-membrane interface. The generate
d microdomains (approximately 1-2 mum in diameter) are dispersed within the
top 8 mum of the surface. The concentration of microdomains was gradually
depleted from the surface to the bulk of the membrane. A schematic of the m
orphology for SMMs within the PES membrane surface was proposed.