Copolymers sensitive to temperature and pH in water and in water+oil mixtures: A DSC, ITC and volumetric study.

Block copolymer micelles are receiving an increasing interest because of the variety of structures and the possibilities to tune them by changing external and internal parameters achieving the desired properties for a specific purpose. We have investigated the acid/base behavior, self-assembling and solubilization ability towards polar oils of star-like copolymers named Tetronics. They are composed of branched four-arms each one consisting of two blocks made of EO and PO units linked to the diethylenediamine group, which confers pH response ability. The copolymers T1107 and T90R4 were studied with a sequential and reverse architecture. The thermodynamics of the acid/base equilibrium was studied by ITC. The aggregation of T1107 in water was analyzed as functions of pH, composition and temperature. The enhanced oil solubilization in the aqueous T1107 aggregates was widely investigated highlighting the role of the oil structure, composition, temperature and pH. As a general result, the oil induces the copolymer aggregation and the solubilization power of micelles is tunable by changing the pH. Efforts have been devoted to model the calorimetric data in order to achieve the thermodynamic properties of the involved process. Finally, we showed that the Tetronic micelles are more promising than the conventional surfactants micelles because of the larger solubilization power and flexibility of the macromolecular system.

Thermodynamics of surfactants, block copolymers and their mixtures in water: the role of the isothermal calorimetry.

The thermodynamics of conventional surfactants, block copolymers and their mixtures in water was described to the light of the enthalpy function. The two methodologies, i.e. the van't Hoff approach and the isothermal calorimetry, used to determine the enthalpy of micellization of pure surfactants and block copolymers were described. The van't Hoff method was critically discussed. The aqueous copolymer+surfactant mixtures were analyzed by means of the isothermal titration calorimetry and the enthalpy of transfer of the copolymer from the water to the aqueous surfactant solutions. Thermodynamic models were presented to show the procedure to extract straightforward molecular insights from the bulk properties.

Adsorption of a dye on clay and sand. Use of cyclodextrins as solubility-enhancement agents.

Laboratory-scale studies were aimed at elucidating the physico-chemical aspects on the removal process of crystal violet (CV) from waters and solid substrates. The laponite clay (RD) and sand were chosen for the double aim at investigating them as CV adsorbents for water treatment and as substrates which mime the soil components. Sand is very effective in removing CV from waters. The cyclodextrins (CDs) were exploited as solubility-enhancement agents to remove CV from the solid substrates. They are powerful solvent media because they extract the CV from sand forming water-soluble CV/CD inclusion complexes and do not show affinity for sand. Optimum performance was shown by the modified CDs (i.e. hydroxypropyl-beta-cyclodextrin and methyl-beta-cyclodextrin). A linear correlation between the logarithm of the equilibrium constant for the CV/CD inclusion complexes formation (K(cpx)) and the maximum amount of CV extracted from sand in the columns experiments at a flow rate of 1.5 ml min(-1) was drawn. This relationship predicts that CDs with K(cpx)<180 M(-1) are not suitable for CV removal from sand. CDs failed to displace CV from RD because they generate the formation of RD clusters where CV remains entrapped.