Iw. Hamley et al., CRYSTALLIZATION OF ALCOHOL ETHOXYLATE DIBLOCK COPOLYMERS FROM BODY-CENTERED-CUBIC MICELLAR PHASES FORMED IN CONCENTRATED AQUEOUS-SOLUTIONS, Macromolecular chemistry and physics, 199(8), 1998, pp. 1753-1758
Crystallization in concentrated aqueous solutions of the alcohol ethox
ylate diblock copolymers C11E40, C15E39 and C17E40 (where C = methylen
e or methyl and E = oxyethylene) has been investigated using small-ang
le X-ray scattering (SAXS), wide-angle X-ray scattering (WAXS) and rhe
ology. It is shown that the gel phase formed in these materials has bo
dy-centred cubic (bcc) symmetry, and that the bcc structure can be mac
roscopically oriented by large amplitude oscillatory shear. At concent
rations above about 55 wt.-% copolymer, crystallization of the poly(ox
yethylene) block occurs at low temperatures, and the effect of crystal
lization from the oriented bcc structure of a 70 wt.-% solution is exa
mined using SAXS/WAXS. Crystallization induces a second phase separati
on, i.e. the semicrystalline lamellar structure resulting from poly(ox
yethylene)-block crystallization is incommensurate with the oriented b
ce structure, with which it coexists at low temperatures. However, cry
stallization produces an unoriented lamellar structure. WAXS indicates
that the poly(oxyethylene) in the diblock copolymer crystallizes in i
ts usual (helical) form.