The confined film
structures and tribological properties of the
dilute aqueous solution of a silicone-based amphiphilic block copolymer,
bis-isobutyl poly(ethylene glycol) (PEG)-14/amodimethicone (BIPA)
copolymer, between mica surfaces were investigated. The BIPA copolymer
existed as positively charged water-soluble aggregates in the solution.
The adsorption behavior of the BIPA copolymer aggregates on a mica
surface from solution was studied using an atomic force microscope
(AFM); the result showed the immediate formation of a uniform adsorbed
BIPA copolymer layer, followed by the gradual deposition of BIPA aggregates
on the top of the adsorbed layer. Friction measurements were carried
out using the surface forces apparatus (SFA) for the confined films
of BIPA copolymer solution between mica surfaces, which revealed two
different sliding film structures depending on the elapsed time after
surface preparation. The sliding film consisting of two adsorbed BIPA
copolymer layers was obtained for a relatively short elapsed time
(not longer than 3 h), which had an extremely low friction coefficient
μ (of the order of 10–5). The sliding film
on the following day (elapsed time of approximately 24 h) had the
structure of a deposited/kinetically trapped BIPA aggregate layer
confined between the opposing adsorbed layers, and the μ values
were within the range from 10–4 to 10–3. Our results suggest that the different elapsed time ranges and
resulting absence or presence of the intervening layer of trapped
aggregates between the absorbed layers determine the tribological
properties of the confined films. Molecular friction mechanisms are
discussed for the two sliding structures, which give insight into
using amphiphilic block copolymer aggregates for a new class of aqueous
lubrication system to design extremely low friction interfaces.