The conformations of three copolymers at the hexane/water interface ha
ve been studied using neutron reflection. The experiment is made possi
ble by using a specially-designed apparatus in which a thin (approxima
tely 10 mum) layer of hexane is spread on a water surface, thus allowi
ng acceptable transmission of a neutron beam incident at a grazing ang
le to the surface. Since none of the polymers used was deuterated, sen
sitivity to the polymer structure was achieved using contrast variatio
n of the two solvents. A triblock copolymer of poly(ethylene oxide)-po
ly(propylene oxide)-poly(ethylene oxide) (F127 of the Pluronic series)
is shown to adopt a conformation that extends beyond the micellar rad
ius in water and, thus, appears quite stretched. A random copolymer of
poly(vinyl alcohol-co-acetate) is shown to adopt a very flat conforma
tion at the interface, forming a dense layer no more than 20 angstrom
thick. While both of these polymers have hydrophobic moieties, hexane
is not a good solvent for either. In contrast, the hydrophobic block o
f a diblock copolymer of poly(dimethylsiloxane)-poly(2-vinylpyridine N
-oxide) is very soluble in hexane, and in this case the hexane appears
to have a much greater influence over the polymer structure. A substa
ntial proportion of the polymer is found on the hexane side of the int
erface.