EFFECT OF SOLVENT QUALITY ON REVERSE MICELLE FORMATION AND WATER SOLUBILIZATION BY POLY(ETHYLENE OXIDE) POLY(PROPYLENE OXIDE) AND POLY(ETHYLENE OXIDE) POLY(BUTYLENE OXIDE) BLOCK-COPOLYMERS IN XYLENE
P. Alexandridis et K. Andersson, EFFECT OF SOLVENT QUALITY ON REVERSE MICELLE FORMATION AND WATER SOLUBILIZATION BY POLY(ETHYLENE OXIDE) POLY(PROPYLENE OXIDE) AND POLY(ETHYLENE OXIDE) POLY(BUTYLENE OXIDE) BLOCK-COPOLYMERS IN XYLENE, Journal of colloid and interface science, 194(1), 1997, pp. 166-173
In addition to associating into (''normal'') micelles in aqueous solut
ions, amphiphilic polyoxyalkylene block copolymers can form ''reverse'
' micelles in organic solvents at sufficiently high copolymer concentr
ations (above the critical micellization concentration (CMC)) and in t
he presence of some water, The effects of solvent quality on the copol
ymer micellization in an organic solvent and on the solubilization of
water in such systems are examined here for representative poly(ethyle
ne oxide)-b-poly(propylene oxide)b-poly(ethylene oxide) (PEO-PPO-PEO)
and poly(butylene oxide)-b-poly(ethylene oxide) (PBO-PEO) copolymers,
The solvent quality is modulated by the addition of cosolutes and by a
change in the temperature. A number of notable observations are repor
ted: Worsening the aqueous solvent conditions by the addition of NaCl
(10 wt% with respect to water) almost doubles the CMC and the water so
lubilization capacity (WS) of a PEO-PPO-PEO copolymer inp-xylene, An i
ncrease in temperature makes water a worse and xylene a better solvent
for the copolymer, The combined result of heating is an increase of t
he CMC for all three copolymers studied, This indicates that the forma
tion of reverse micelles is exothermic, which is opposite to what has
been observed for normal micelles, The effects of temperature on the w
ater uptake are nonmonotonic: WS increased with temperature for a PEO-
PPO-PEO copolymer with 40% PEO but decreased for a copolymer with 20%
PEG. An increase in WS with temperature, followed by a decrease, with
the maximum WS efficiency occurring at the ''effective'' cloud point o
f the copolymer is proposed in order to explain this observation. (C)
1997 Academic Press.