The concentration interval of 48−62 wt % hexaethylene glycol
n-hexadecyl ether (C16EO6) in
deuterium
oxide (2H2O) has been investigated using
optical microscopy, 2H nuclear magnetic resonance, and
small
angle X-ray scattering and the detailed phase behavior established.
On cooling from the lamellar phase
(Lα), the phase sequence defected lamellar
(Lα
H), mesh intermediate (Int.),
Ia3d cubic (V1), and
hexagonal
(H1) or hexagonal plus gel biphase (H1 +
Lβ) was observed. On heating from the hexagonal or
two-phase
region, the region of intermediate and cubic phases formed on cooling
is replaced by an Ia3d cubic phase.
The mesh intermediate phase, formed on cooling, is demonstrated to
have a rhombohedral structure,
assigned the space group R3̄m. It
represents a phase in which the water-filled defects of the
higher
temperature Lα
H phase become correlated
between layers. The formation of the phase is driven by
the
need to introduce more curvature into the interface as the temperature
is decreased because of increased
ethylene oxide head group (EO) hydration. The interlayer
correlation arises from the strong, repulsive
head group overlap interaction in this system.