Inulin, a polydisperse reserve polysaccharide, has prospective uses in food, pharmacy, and industry. Its uses and applications often encounter interactions with lipids and amphiphiles. Reports on such interactions are scarcely found in literature. In the present study, we have examined the nature of interactions between inulin and cationic amphiphiles, alkyltrimethylammonium bromides (CnTAB: n=12, 14, 16, 18), over a fair range of concentrations for both the polymer and the amphiphile. At low concentration, small induced amphiphile aggregates form complexes with inulin; at moderate concentration, the complexed inulin self-aggregates leading to coacervate formation, and at higher concentration, the amphiphile forms free micelles in solution. Tensiometric, conductometric, viscometric, and turbidimetric methods have been employed to study the above phenomena. The isolated coacervates of inulin with C18TAB were examined by scanning electron microscopy (SEM), transmission electron microscopy (TEM), atomic force microscopy (AFM), differential scanning calorimetry (DSC), thermogravimetry (TG), and differential thermal analysis (DTA) to ascertain their morphology, structure, and thermal stability.

This article deals with the solution properties of poly(vinylpyrrolidone) (PVP) in salt and surfactant environment. The cloud point (CP) of PVP has been found to be induced by the salts NaCl, KCl, KBr, Na2SO4, MgSO4, and Na3PO4. On the basis of CP values for a salt at different [PVP], the energetics of the clouding process have been estimated. The effect of the surfactant, sodium dodecyl sulfate (SDS), on the salt-induced CP has also been studied, and reduction in CP at low [SDS] and increase in CP at high [SDS] have been observed. The water vapor adsorption of PVP has been determined by isopiestic method. The results display a BET Type III isotherm whose analysis has helped to obtain the monolayer capacity of PVP and formation of multilayer on it. The solvation of PVP in a solution of water and a water-isopropanol mixture has been determined by conductometry from which contribution of the individual components were estimated. The interaction of PVP with SDS in solution led to formation of a complex entity, which has been studied also by conductometry adopting a binding-equilibrium scheme. SDS has been found to undergo two types of binding as monomers in the pre- critical aggregation concentration (CAC) range and as small clusters in the post CAC region. The stoichiometries of binding and binding constant were evaluated.

We report a facile design and synthesis of magnetic iron oxide (IO) incorporated chitosan-graphene oxide (CSGO) hydrogel nanocomposites (CSGOIO) by employing in situ mineralization of iron ions in a hydrogel matrix. The mechanism of their formation was investigated by various physical methods, viz., FTIR, XRD, VSM, TGA, SEM, TEM, and BET. This approach was shown to have a direct impact on the morphological features and the structural order of the nanocomposites. The potential of the prepared nanocomposites for effective removal of a cationic dye, methylene blue (MB), from aqueous solution was investigated by performing a series of batch adsorption experiments, in line with the effect of adsorbent dosage, initial dye concentration, contact time, pH, ionic strength, and temperature. The adsorption was fairly influenced by the pH and ionic strength of the medium, indicating an electrostatic interaction between the adsorbent and MB molecules. The kinetics of adsorption followed a pseudo-second-order model, and equilibrium capacity was described by the Freundlich adsorption model. Interestingly, the nanocomposites exhibited a fast removal performance with a rate constant of 0.06 g mg–1 min–1. The hydrogel nanocomposites were found to possess an excellent adsorptive property after four successive cycles at different pH of the solution, thus providing a cost-effective material for dye removal applications. Therefore, this material, enabling dye removal in a wide variety of solution conditions, offered a promising platform for sustainable development of water purification technology.

Physicochemical properties viz., aggregation, molar mass, shape, and size of chicory inulin in solution were determined by fluorimetry, DLS, SLS, TEM, and viscometry methods. The thermal stability of the biopolymer was examined by TGA, DTA, and DSC measurements. The water vapor adsorption of desiccated inulin was also studied by the isopiestic method, and the data were analyzed in the light of the BET equation. On the basis of the obstruction to ion conductance by the inulin aggregates in solution and analysis of the data, the extent of hydration of inulin in solution was estimated. The result was coupled with the intrinsic viscosity, [eta], of inulin to ascertain the shape of the biopolymer aggregates in aqueous solution. The critical aggregation concentration (cac) of inulin in aqueous as well as in salt solution was assessed by fluorimetry. The weight average molar mass, Mw , of inulin monomer and its aggregate was found to be 4468 and 1.03 x 10(6) g/mol, respectively, in aqueous solution. This aggregated mass was 2.4 x 10(6) g/mol in 0.5M NH(4)SCN solution. The [eta] values of the soft supramolecular aggregates in solution (without and with salt) were small and comparable with globular proteins evidencing spherical geometry of the biopolymer aggregates as supported by the TEM results. In DMSO, rod-like aggregates of inulin was found by the TEM study. The [eta] of the biopolymer in the DMSO medium was therefore, higher than that in the aqueous medium. Unlike aqueous medium, the aggregation in DMSO was not associated with a cac.

The surface activity of isopropanol (IP) and poly(vinylpyrrolidone) (PVP) at the air/water interface has been studied. The self-aggregation of sodium dodecyl sulfate (SDS) in IP-water as well as in IP-PVP-water media has been investigated using physical methods, viz., tensiometry, conductometry, calorimetry, and viscometry. The interaction of SDS with PVP in IP-water medium as well as its self-aggregation (or micellization) in the presence of PVP has been assessed. The results reveal a fair degree of surface activity of IP in aqueous medium, which is only moderate for PVP. The critical micellar concentration (CMC) of SDS passes through a minimum at (v/v) % IP = 6.62. SDS interacts with PVP, yielding a critical aggregation concentration (CAC) at a low [SDS], independent of IP content in the medium. At a higher [SDS], free micelle formation takes place in solution, which is lower in mixed solvent than in water and is independent of solvent composition by tensiometry, but not by conductometry and calorimetry. The viscosity of micelle-interacted PVP in solution takes a long time to stabilize, whereas, for non-interacting additives, such as NaCl and cetyltrimethylammonium bromide (CTAB), it is time independent.

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{[Cu(2)(H(2)L)(OH)(H(2)O)].(ClO(4))(2)(H(2)O)} (1) serves as a selective azide ion fluorescent sensor in aqueous medium. 1 binds with N(3)(-) to give [Cu(6)(HL)(2)(mu(1,1)-N(3))(6)] (2) which imposes rigidity and decreases the non-radiative decay of the excited state to give rise to fluorescent enhancement. 1 is highly selective over other various anions in aqueous medium.