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Understanding viscosity reduction of a long-tail sulfobetaine viscoelastic surfactant by organic compounds

机译:了解有机化合物降低长尾磺基甜菜碱粘弹性表面活性剂的粘度

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Though the transition from cylindrical micelles to spherical micelles of the anionic surfactant potassium oleate in the presence of oils has been studied, these changes have not been studied for long-tail zwitterionic surfactants. The effects of n-decane, crude oil (CO), extra virgin olive oil (EVOO) and polyglycolic acid (PGA) on the zero-shear viscosity of an aqueous solution of a sulfobetaine surfactant system were investigated at 30 °C and 60 °C. The main surfactant in the system was erucamidopropyl hydroxypropyl sulfobetaine. The methods employed were rheology and cryo-TEM. The solution with 3.96 wt% surfactant system and 6.2 wt% CaCl2 was viscoelastic at both test temperatures due to the formation of entangled cylindrical micelle networks. n-Decane induced the following regimes of zero-shear viscosity change at both temperatures: (i) the high viscosity regime (HVR), (ii) the transition regime (TR), and (iii) the low viscosity regime (LVR). The HVR was characterized by high zero-shear viscosities. The TR was characterized by a sharp drop in zero-shear viscosity due to the formation of untangled micelles. The LVR was due to the formation of microemulsions. The formation of these regimes depended on the balance between micellization and oil solubilization. We reveal for the first time that the number of regimes depends on the type of oil: both CO and EVOO induced only one and two regimes at 30 °C and 60 °C, respectively. PGA did not significantly affect the solution at either temperature with increasing concentration, meaning the solution was resistant to decreasing pH even at higher temperatures.
机译:尽管已经研究了在油存在下阴离子表面活性剂油酸钾从圆柱形胶束到球形胶束的转变,但是对于长尾两性离子表面活性剂,尚未研究这些变化。研究了 n 癸烷,原油(CO),初榨橄榄油(EVOO)和聚乙醇酸(PGA)对磺基甜菜碱表面活性剂体系水溶液零剪切粘度的影响。在30°C和60°C下。该体系中的主要表面活性剂是金刚烷丙基丙基羟丙基磺基甜菜碱。采用的方法是流变学和低温TEM。由于缠结的圆柱形胶束网络的形成,具有3.96 wt%的表面活性剂体系和6.2 wt%的CaCl 2 的溶液在两个测试温度下均具有粘弹性。 n -癸烷在两种温度下均引起以下零剪切粘度变化:(i)高粘度(HVR),(ii)过渡(TR)和(iii)低粘度方案(LVR)。 HVR的特点是高零剪切粘度。 TR的特征在于由于形成缠结的胶束而使零剪切粘度急剧下降。 LVR是由于微乳液的形成。这些机制的形成取决于胶束化和油增溶之间的平衡。我们首次揭示出,状态的数量取决于油的类型:CO和EVOO分别在30°C和60°C时仅诱发一种和两种状态。在任一温度下,随着浓度的升高,PGA均不会显着影响溶液,这意味着即使在较高温度下,溶液也能抵抗pH值的降低。

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