U. Kastner et al., INTERACTIONS BETWEEN MODIFIED HYDROXYETHYL CELLULOSE (HEC) AND SURFACTANTS, Colloids and surfaces. A, Physicochemical and engineering aspects, 112(2-3), 1996, pp. 209-225
The macroscopic properties of aqueous solutions of several modified hy
droxyethyl cellulose (HEC) samples and their interactions with anionic
and cationic surfactants are studied by solubility, electric birefrin
gence, rheology, and surface tension measurements. The modified HEC sa
mples carry cationic groups (cat-HEC, A), cationic and hydrophobic gro
ups in random distribution (HM-cat-HEC, B), or both cationic and hydro
phobic groups at the same substituent (cat-HMHEC, C). The cat-HEC poly
mers behave like typical polyelectrolytes, while the additionally hydr
ophobic samples B and C combine the solution properties of both charge
d and hydrophobic polymers. On the addition of an oppositely charged s
urfactant all polymer solutions show similar phase behavior of associa
tive phase separation at certain amounts of surfactant, followed by re
solubilization with excess surfactant concentrations. The hydrophobic
and cationic parts of samples B and C interact synergistically with th
e anionic surfactant molecules, resulting in stronger viscoelastic pro
perties than for only cationic HEC. Furthermore, the hydrophobic parts
also allow cooperative interactions with surfactants of the same char
ge. Nevertheless, differences are found for these hydrophobic and cati
onic derivatives depending on whether the charges and the hydrophobic
parts are separately attached at the polymer backbone (sample B) or be
long to one substituent (sample C). On the addition of anionic surfact
ants sample B forms a strong gel in the pre-precipitation area and a d
ilute sol in the post-precipitation area, while sample C forms highly
viscoelastic gels in both the pre-precipitation and post-precipitation
areas. A viscosity enhancement with increasing cationic surfactant co
ncentration is observed only for sample B.