The shape, size, aggregation, hydration, correlation times, and thermodynamic studies on macromonomer micelles
- 1 December 1996
- journal article
- research article
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 105 (21) , 9649-9656
- https://doi.org/10.1063/1.472809
Abstract
The hydration of the macromonomer micelles has been directly determined from the measurements of conductance of micellar solutions of macromonomer in 5 mM NaCl using the principle of the obstruction of electrolyte migration by the surfactants. This coupled with the intrinsic viscosity has helped in evaluating asymmetry of the micellar particles and their average axial ratios. The hydration has also been determined by Einstein and Vand’s equations, and are in good agreement with the conductivity results. Hydration number and micellar sizes are variable with temperature. The shape of the macromonomer micelles has been observed to be more or less spherical at 15 °C. However, above 15 °C the shape of the micelles are ellipsoids. From the absolute values of the axes, the micellar volume, hydrodynamic radius, radius of gyration, frictional, and diffusional coefficients as well as translational (τ D ), rotational (τ r ), and effective correlation (τ a ) times have been calculated. τ r values for Triton X‐100, Tween‐20, Tween‐80, and macromonomer at 25 °C are 45, 28, 25, and 8 ns, respectively. The aggregation number N̄ of the macromonomer in an aqueous solution was determined by fluorescence spectroscopic technique. Blueshift of ANS emission was observed in the presence of macromonomer micelles. Both N̄ and the Stern–Volmer rate constant (K SV) are variable with temperature and found them to be maximum at 25 °C indicating the macromonomer micelles attained a state of fully extended conformation at 25 °C. Diffusion energy (E D ) of the macromonomer micelles in water has been calculated and found to be 21.0 and 21.1 kJ mol−1 for oblate and prolate models, respectively. The partial molal volume of the macromonomer micelles has also been determined and its comparison with the molar volume of pure macromonomer suggested a volume contraction due to immobilization of the water phase by the hydrophilic head groups of macromonomer. Thermodynamic activation parameters for viscous flow are in favor of the formation of structured water by the presence of macromonomer micelles. Enthalpy (ΔH*) and entropy (ΔS*) values show a very good compensation between them.Keywords
This publication has 51 references indexed in Scilit:
- Aggregation, hydrogen bonding and thermodynamic studies on Boc-Val-Val-Ile-OMe tripeptide micelles in chloroformJournal of the Chemical Society, Faraday Transactions, 1994
- Synthesis, characterization, and micelle formation in an aqueous solution of methoxypolyethylene glycol macromonomer, homopolymer, and graft copolymerMacromolecules, 1993
- Poly(ethylene oxide) macromonomers. 7. Micellar polymerization in waterMacromolecules, 1991
- Synthesis and Polymerization of Surface-Active Sodium AcrylamidoundecanoateJournal of Macromolecular Science: Part A - Chemistry, 1989
- Light scattering from aqueous solutions of a nonionic surfactant (C14E8) in a wide concentration rangeThe Journal of Physical Chemistry, 1988
- Nonionic rodlike micelles in dilute and semidilute solutions: intermicellar interaction and the scaling lawThe Journal of Physical Chemistry, 1988
- Kinetics and mechanism of emulsifier‐free emulsion polymerization: Styrene/surface active ionic comonomer systemJournal of Polymer Science: Polymer Chemistry Edition, 1985
- Size and shape of nonionic amphiphile (C12E6) micelles in dilute aqueous solutions as derived from quasielastic and intensity light scattering, sedimentation, and pulsed-field-gradient nuclear magnetic resonance self-diffusion dataThe Journal of Physical Chemistry, 1983
- Examination of the lamellar phase of aerosol OT/water using pulsed field gradient nuclear magnetic resonanceThe Journal of Physical Chemistry, 1983
- Temperature Dependence of the Heats of Solution of Poly(ethylene glycol) and of Related CompoundsBulletin of the Chemical Society of Japan, 1970