1Department of Chemistry, Kisan Arts, Commerce and Science College Parola, Tal. Parola, Dist. Jalgaon425111, Maharashtra, India
2Department of Chemistry, ttamrao Patil Arts and Science College, Dahivel, Tal. Sakri, Dist. Dhule424304, Maharashtra, India
*Corresponding Author E-mail: kirandpatil22@gmail.com
The interaction between poly (acrylic acid) (PAA, MW ≈ 50,000) and dodecyl trimethyl ammonium bromide (DTAB) was investigated in aqueous solution using ultrasonic interferometry, density, viscosity, and conductivity. Experiments were performed with 0.1 M DTAB containing 0–1.0 wt/v %, PAA (at 0.2 % interval) at 298.15–313.15 K. Density and viscosity increased with PAA concentration, indicating enhanced solutesolvent interactions. Non-linear trends in reduced viscosity and relaxation time, with minima near 0.4 wt/v% PAA, suggested micelle disruption followed by cooperative polymer-micelle association. Ultrasonic velocity rose sharply (1520 → 1732 m/s) and compressibility decreased at 0.4 wt/v%, confirming compact micelle–polymer complex formation. At higher temperatures, maxima shifted to ~0.6 wt/v%, reflecting reorganization into elongated aggregates. Rheological and conductivity data supported temperature-dependent micellar hydration, counterion binding, and shape transitions. Overall, PAA significantly modulates DTAB micellization through hydrophobic and electrostatic interactions, with concentration- and temperature-dependent transitions between compact and elongated micelle–polymer assemblies. These findings provide thermodynamic and structural insight into polymer–surfactant systems with relevance to pharmaceutical, detergent, and colloidal formulations.
Ultrasonic velocity, Viscosity, Adiabatic compressibility, Surfactant-polymer interactions, Micelle, DTAB, Polyacrylic acid