ABSTRACT
The viscoelasticity of wormlike micelles composed of ionic surfactants typically shows an exponential decrease with increasing temperature, which limits their application in relatively high-temperature (>90.0 °C) oilfields and the synthesis of functional materials as supramolecular templates at high temperatures. In this work, a series of imidazolium gemini surfactants, 1,9-(ethane-1,2-diyl)bis(3-alkyl-1H-imidazol-3-ium) bromide ([Cn-2-Cnim]Br2, n = 12, 14, 16, 18, 20), were synthesized. Their surface activities and aggregation behaviors in water were studied by electrical conductivity, rheology, polarization optical microscopy, small-angle X-ray scattering, ζ potential, and hydrogen nuclear magnetic resonance measurements. [C12-2-C12im]Br2 and [C14-2-C14im]Br2 mainly precipitate in water. [Cn-2-Cnim]Br2 (n = 16, 18, 20) forms lamellar liquid crystals over a large range of concentrations at low temperatures. With the increase of temperature, the lamellar liquid crystals transit to wormlike micelles. Interestingly, the viscoelasticity of the three wormlike micelles first increases to the maximum and then decreases with increasing temperature. These wormlike micelles without additives retain high viscoelasticity up to 90.0 °C or above. With the increase of the alkyl chain length of the surfactants, the transition temperature of lamellar liquid crystal to wormlike micelles and the disintegration temperature of wormlike micelles increase. The unusual increase of the viscoelasticity of wormlike micelles was due to the desorption of weakly bound counterions and the extension of the long hydrophobic chains of surfactants at high temperatures.
ABSTRACT
In this study, flower-like porous iron doped bismuth oxybromide on porous activated carbon visible light catalysts (BiOBr/Fe@AC) were prepared by a reactive imidazole ionic liquid surfactant assisted solvothermal process. The morphologies, structures, optical properties and photocatalytic properties were investigated in detail. The morphology of the synthesized Fe doped BiOBr composites gradually changed from a regular spherical shape to a non-specific shape with the increase of the alkyl chain length of the ionic liquid surfactants. The photocurrent of BiOBr/Fe@AC composites is greatly influenced by the content of Fe, the type of carbon sphere and the size of the composites. The photocatalytic activity of the obtained BiOBr/Fe@AC composites was evaluated by the degradation of 2-chloroethyl sulfide (CEES) under visible light. The BiOBr/Fe@AC composites exhibited significantly enhanced photocatalytic performance compared to that of pure BiOBr and the 10.0% Fe doped BiOBr/Fe@AC composite displayed the highest photocatalytic activity. The main active species were determined to be holes and superoxide radicals by electron spin resonance (ESR) analysis and free radical trapping experiments. The introduction of iron can improve the separation and transfer rate of photoinduced charges. Carbon spheres can enhance light harvesting, improve electron transfer and increase the number of catalytic active sites. Iron and carbon embellishment is an effective strategy to enhance the photocatalytic efficiency of BiOBr. Finally, a possible photocatalytic mechanism of BiOBr/Fe@AC has been proposed.