A monolayer network film of a phenolic resin was produced through the
Langmuir-Blodgett (LB) technique. Amphiphilic phenols, o-, m- and p-he
xadecoxyphenol (o-, m- and p-HP), were synthesized by the reactions of
catechol, resorcinol, and hydroquinone, respectively, with 1-iodohexa
decane. Monolayers of the HPs were spread on aqueous subphases with di
fferent pHs and on aqueous 1% formaldehyde subphase. The surface press
ure-area isotherms revealed characteristic monolayer behaviors accordi
ng to the structural isomers at the air-water interface. Spontaneous i
ncrease of the surface pressure by the reaction of the phenol moiety w
ith formaldehyde at the air-water interface was found on the aqueous f
ormaldehyde subphase. The p-HP monolayer was transferred onto calcium
fluoride substrate as Y-type and the molecular structure was determine
d by the Fourier transform infrared spectroscopy (FTIR). Acid and foll
owing heat treatments were applied for the enhancement of network form
ation. The network film showed resistance toward organic solvents. The
mechanical stability of the network film was indirectly evaluated by
the scanning electron microscopy (SEM) observation of the LB film morp
hology covered over the porous substrate and less than eight layers we
re enough to cover the pores of 0.1 mu m diameter. (C) 1998 Elsevier S
cience S.A. All rights reserved.