ABSTRACT
The use of polymer gels for the removal of toxic chemicals from wastewater is an important area in terms of both academic and industrial research. This work presents a simple approach to the fabrication of chemically cross-linked cationic hydrogel adsorbents using designed ionic liquid-based cross-linkers and their successful use in the removal of organic dyes. Two different ionic liquid cross-linkers, [VIm-4VBC][Cl] (ILA)/[DMAEMA-4VBC][Cl] (ILB), are synthesized by the simple nucleophilic substitution reaction of 4-vinylbenzyl chloride (4VBC) separately with 1-vinylimidazole (VIm) and 2-(dimethylamino)ethyl methacrylate (DMAEMA). Cross-linked poly(acrylamide) (CPAam) and poly(2-hydroxyethyl methacrylate) (CPHEMA) hydrogels are then prepared from the corresponding monomers and as-synthesized cross-linkers (ILA and ILB) by free radical polymerization in the presence of a redox initiator combining ammonium persulfate (APS) and N,N,N',N'-tetramethylethylenediamine (TEMED). The dried CPAam and CPHEMA xerogels exhibit macroporous morphology and high thermal stability. The hydrogel samples exhibit high swelling behavior, and the diffusion of water molecules into the hydrogels follows pseudo-Fickian kinetics. The cationic cross-linking sites in the hydrogel networks allow preferable binding with anionic dyes, and these dye uptake capacities are determined using different model anionic dyes via UV-vis spectroscopy. The dye adsorption onto these hydrogels follows a pseudo-second-order kinetic model. The adsorption mechanism is also analyzed by employing intraparticle diffusion and Boyd kinetic models. The relationship between the maximum equilibrium adsorption capacity (qm) of the hydrogels for eosin B (EB) dye and the equilibrium EB concentration can be better described by Langmuir and Freundlich isotherm models, and the estimated qm using the Langmuir isotherm can reach more than 100 mg g-1. The cross-linked hydrogels can be easily regenerated and have a recycling efficiency of >80% for up to three consecutive dye adsorption-desorption cycles, which is promising for their use in wastewater treatment.
ABSTRACT
The discovery of new phenomena in layered and nanostructured magnetic devices is driving rapid growth in nanomagnetics research. Resulting applications such as giant magnetoresistive field sensors and spin torque devices are fuelling advances in information and communications technology, magnetoelectronic sensing and biomedicine. There is an urgent need for high-resolution magnetic-imaging tools capable of characterizing these complex, often buried, nanoscale structures. Conventional ferromagnetic resonance (FMR) provides quantitative information about ferromagnetic materials and interacting multicomponent magnetic structures with spectroscopic precision and can distinguish components of complex bulk samples through their distinctive spectroscopic features. However, it lacks the sensitivity to probe nanoscale volumes and has no imaging capabilities. Here we demonstrate FMR imaging through spin-wave localization. Although the strong interactions in a ferromagnet favour the excitation of extended collective modes, we show that the intense, spatially confined magnetic field of the micromagnetic probe tip used in FMR force microscopy can be used to localize the FMR mode immediately beneath the probe. We demonstrate FMR modes localized within volumes having 200 nm lateral dimensions, and improvements of the approach may allow these dimensions to be decreased to tens of nanometres. Our study shows that this approach is capable of providing the microscopic detail required for the characterization of ferromagnets used in fields ranging from spintronics to biomagnetism. This method is applicable to buried and surface magnets, and, being a resonance technique, measures local internal fields and other magnetic properties with spectroscopic precision.
