Application of chitosan, a natural aminopolysaccharide, for dye removal from aqueous solutions by adsorption processes using batch studies: A review of recent literature

Intermolecular And Surface Forces

Structure and reactivity of water at biomaterial surfaces

In the past few years, spiropyran has emerged as the molecule-of-choice for the construction of novel dynamic materials. This unique molecular switch undergoes structural isomerisation in response to a variety of orthogonal stimuli, e.g. light, temperature, metal ions, redox potential, and mechanical stress. Incorporation of this switch onto macromolecular supports or inorganic scaffolds allows for the creation of robust dynamic materials. This review discusses the synthesis, switching conditions, and use of dynamic materials in which spiropyran has been attached to the surfaces of polymers, biomacromolecules, inorganic nanoparticles, as well as solid surfaces. The resulting materials show fascinating properties whereby the state of the switch intimately affects a multitude of useful properties of the support. The utility of the spiropyran switch will undoubtedly endow these materials with far-reaching applications in the near future.

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Spiropyran-based dynamic materials

Multilayer thin films have garnered intense scientific interest due to their potential application in diverse fields such as catalysis, optics, energy, membranes, and biomedicine Here we review the current technologies for multilayer thin-film deposition using layer-by-layer assembly, and we discuss the different properties and applications arising from the technologies We highlight five distinct routes of assembly—immersive, spin, spray, electromagnetic, and fluidic assembly—each of which offers material and processing advantages for assembling layer-by-layer films Each technology encompasses numerous innovations for automating and improving layering, which is important for research and industrial applications Furthermore, we discuss how judicious choice of the assembly technology enables the engineering of thin films with tailor-made physicochemical properties, such as distinct-layer stratification, controlled roughness, and highly ordered packing

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Technology-driven layer-by-layer assembly of nanofilms

The role of particles in stabilising foams and emulsions

Surface chemistry-rheology relationships in concentrated mineral suspensions

Zeta potentials and yield stresses of silica suspensions in concentrated monovalent electrolytes: isoelectric point shift and additional attraction

The interaction of water and the alumina surface is comprehensively reviewed. Water can be incorporated in the alumina crystal structure resulting in the formation of aluminum hydroxides such as gibbsite. Alumina dissolves into water to an extent that depends primarily upon the solution pH and temperature. The soluble Al (III)aq species (hydrolysis products) likewise depend upon the solution pH, temperature, aluminum, and other salt concentrations. The development of charge on the surface of alumina is controlled by amphoteric surface ionization reactions. The charging behavior of both alumina powders and single crystal faces is compared. The differences can be explained by the reactivities of different types of surface hydroxyl groups. The substantial difference in surface charging behavior of single crystal sapphire and alumina powders indicates that experiments and modeling conducted on single crystals is of limited use in predicting suspension behavior. The atomic scale structure of the hydroxylated sapphire (0001) basal plane is nearly identical to the gibbsite (001) basal plane. The observed surface structures are consistent with the charging behavior of the surfaces. The role of surface charge on the adsorption of processing additives is briefly discussed. How surface charge and processing additives at the alumina aqueous solution interface influence surface forces between particles is reviewed. The influence of these forces on suspension properties such as rheological behavior is outlined. The importance of controlling these behaviors to improve colloidal ceramic powder processing is stressed.

Charging Behavior at the Alumina–Water Interface and Implications for Ceramic Processing

Three cationic polymers with molecular weights and charge densities of 3.0 x 10(5) g/mol and 10%, 1.1 x 10(5) g/mol and 40%, and 1.2 x 10(5) g/mol and 100% were chosen as flocculants to aggregate silica particles (90 nm), under various conditions, including change in polymer dosage, particle concentration, background electrolyte concentration, and shear rate. The size and structure of flocs produced were determined using the static light scattering technique. On the basis of measurements of polymer adsorption and its effect on the zeta potential and floc properties, it has been found that the polymer charge density plays an important role in determining the flocculation mechanism. Polymers with a 10% charge density facilitate bridging, 40% charged polymers bring about either a combination of charge neutralization and bridging or bridging, depending on the polymer dosage, and polymers with the charge density of 100% induce electrostatic patch flocculation mechanism at the optimum polymer dosage and below but bring about bridging mechanism at the polymer dosage approaching the adsorption plateau value. Bridging aggregation can readily be affected by the particle concentration, and an increase in particle concentration results in the formation of larger but looser aggregates, whereas electrostatic patch aggregation is independent of particle concentration. The addition of a background electrolyte aids in bridging aggregation while it is detrimental to electrostatic patch aggregation. It has also been found that the effect of shear rate on the mass fractal dimension depends on polymer charge density.

George V. Franks

Papers

The role of particles in stabilising foams and emulsions

Surface chemistry-rheology relationships in concentrated mineral suspensions

Zeta potentials and yield stresses of silica suspensions in concentrated monovalent electrolytes: isoelectric point shift and additional attraction

Charging Behavior at the Alumina–Water Interface and Implications for Ceramic Processing

Flocculation Mechanism Induced by Cationic Polymers Investigated by Light Scattering