The chemistry underlying the aqueous dispersibility of graphene oxide (GO) and reduced graphene oxide (r-GO) is a key consideration in the design of solution processing techniques for the preparation of processable graphene sheets. Here, we use zeta potential measurements, pH titrations, and infrared spectroscopy to establish the chemistry underlying the aqueous dispersibility of GO and r-GO sheets at different values of pH. We show that r-GO sheets have ionizable groups with a single pK value (8.0) while GO sheets have groups that are more acidic (pK = 4.3), in addition to groups with pK values of 6.6 and 9.0. Infrared spectroscopy has been used to follow the sequence of ionization events. In both GO and r-GO sheets, it is ionization of the carboxylic groups that is primarily responsible for the build up of charge, but on GO sheets, the presence of phenolic and hydroxyl groups in close proximity to the carboxylic groups lowers the pKa value by stabilizing the carboxylate anion, resulting in superior water dispersibility .

The electrochemical performance of polymer‐based batteries can be improved by the addition of inorganic fillers to the polymer electrolyte, giving composite polymer electrolytes. The use of polymer nanocomposites, where the dimensions of the filler particles are reduced, should lead to the improvement of the performance of the electrolytes. Here, the direct intercalation of poly(ethylene oxide) into Na⊕ and Li⊕‐exchanged layered silicates and the properties of the resulting nanocomposites is reported.

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An attempt has been made to understand the hydrogeochemical parameters to develop water quality index in Thirumanimuttar sub-basin. A total of 148 groundwater samples were collected and analyzed for major cations and anions. The domination of cations and anions was in the order of Na>Mg>Ca>K for cations and Cl>HCO(3) >SO(4) in anions. The hydrogeochemical facies indicate alkalis (Na and K) exceed alkaline earths (Ca and Mg) and strong acids (Cl and SO(4)) exceed weak acid (HCO(3)). Water quality index rating was calculated to quantify overall water quality for human consumption. The PRM samples exhibit poor quality in greater percentage when compared with POM due to effective leaching of ions, over exploitation of groundwater, direct discharge of effluents and agricultural impact. The overlay of WQI with chloride and EC correspond to the same locations indicating the poor quality of groundwater in the study area. SAR, Na%, and TH were noted higher during both the seasons indicating most of the groundwater locations not suitable for irrigation purposes.

Infrared and Raman spectroscopy have been used to establish the conformation and orientation of the methylene “tail” of cetyl trimethylammonium ions intercalated in an inorganic layered host, CdPS3. Intercalation, effected by a two-step ion-exchange process leading to the formation of Cd0.83PS3(CTA)0.34, occurs with a lattice dilation of 26.5 Å with the surfactant ions within the galleries adopting a bilayer structure. The frequencies of the conformationally sensitive methylene stretching modes in the infrared and Raman spectra indicate that a majority of the bonds in the methylene chain are in a trans conformation. The methylene chains are tilted with respect to the inorganic layer. The tilt angle as determined from orientation-dependent infrared spectra is ∼35°. Although the population of gauche conformers is low, it has been possible to identify specific conformational sequences containing a gauche bond, in the interior and termini of the intercalated methylene chains, by their characteristic frequencies in the infrared spectrum. These high-energy conformers, except for the ones at the chain end, disappear on cooling, leaving on average all 15 methylene units of the intercalated cetyl trimethylammonium ion in trans conformational registry at 40 K. The terminal gauche defects are significant in preventing interdigitation of the low-density intercalated surfactant bilayer.