D. Sohn et al., MONOLAYER PROPERTIES OF A FUZZY ROD POLYMER - POLY(GAMMA-STEARYL-ALPHA, L-GLUTAMATE), Journal of polymer science. Part B, Polymer physics, 34(17), 1996, pp. 3025-3034
Static and dynamic properties, and surface morphologies of monolayers
at the air-water interface of a fuzzy rod polymer, poly(gamma-stearyl
alpha, L-glutamate), PSLG, have been examined by the Wilhelmy plate me
thod for surface pressure, electrically induced capillary wave die-act
ion (ECWD), epi-fluorescence microscopy, and atomic force microscopy (
AFM). The monolayers were first formed by spreading polymer solutions
at the air-water interface and allowing the solvent to evaporate to ob
tain polymer films, i.e., spread monolayers. The surface mass density
was varied by either successive additions of more solutions on a given
surface area or step-wise compression of the surface barrier an a Lan
gmuir trough. Surface pressure isotherms at 23-60 degrees C were confi
rmed to be reversible and reproducible, and an abrupt change at approx
imately 60 degrees C was observed, which is reported as the melting po
int of crystalline stearyl side chains. By AEM, the monolayer director
n by surface alignment was confirmed as perpendicular to the compress
ion direction and certain islands of departure from the monolayer stat
e were visualized upon transferring the monolayers horizontally to sil
icon wafers. Macroscopic anisotropy in the surface alignment was probe
d by the electrocapillary waves propagated perpendicular (perpendicula
r to) and parallel (//) to the director n; the surface tension anisotr
opy amount to about 7% difference, sigma perpendicular to/sigma(//) <
0.07, where a is the surface tension deduced from the wave propagation
characteristics. Multidomain morphologies of the monolayers were imag
ed by epi-fluorescence microscopy and they were found to differ accord
ing to the method of monolayer mass density variation, i.e., the succe
ssive addition and step-wise compression. (C) 1996 John Wiley & Sons,
Inc.