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Thermoreversible viscoelastic to weak gel transition in a micellar ionic liquid with salt

机译:含盐的胶束离子液体中的热可逆粘弹性到弱凝胶转变

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Rheological measurements as a function of temperature have been carried out on a micellar-ionic liquid (4.45. wt% sodium dodecylsulfate (SDS) in 1-butyl-3-methylimidazolium chloride (BmimCl)) with 18.7. wt% lithium chloride (LiCl). We report here for the first time, the formation of a " weak gel" state at high temperatures (>80. °C) based on elastic and loss moduli behavior and yield stress measurements. Below 80. °C, the sample is identified to be in a viscoelastic liquid state. The transition from viscoelastic liquid to weak gel state is found to be thermoreversible. From the rheological evolutions, small angle neutron scattering measurements and turbidity measurements, we argue that the weak gel state arises due to the winning of the micellar network structures over the association structure of BmimCl in the presence of lithium chloride and is responsible for the viscoelastic liquid to weak gel transformation observed in the micellar-ionic liquid.
机译:已经在18.7的胶束离子液体(在1-丁基-3-甲基咪唑鎓氯化物(BmimCl)中的4.45重量%的十二烷基硫酸钠(SDS))上进行了随温度变化的流变学测量。重量百分比的氯化锂(LiCl)。我们在此首次报告,基于弹性和损耗模量行为以及屈服应力测量结果,在高温(> 80。C)下形成“弱凝胶”状态。低于80°C,样品被鉴定为处于粘弹性液体状态。发现从粘弹性液体到弱凝胶状态的转变是热可逆的。从流变学演变,小角度中子散射测量和浊度测量来看,我们认为弱的凝胶态是由于在氯化锂的存在下胶束网络结构胜过BmimCl的缔合结构而形成的,并导致了粘弹性液体在胶束离子液体中观察到微弱的凝胶转化。

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