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Micellization Behavior of Conventional Cationic Surfactants within Glycerol-Based Deep Eutectic Solvent

机译:甘油基深对共晶溶剂中常规阳离子表面活性剂的胶束化行为

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The aggregation behavior of two cationic surfactants, i.e., cetyldimethylethanolammonium bromide (CDMEAB) and cetyltributylphosphonium bromide (CTBPB), within an aqueous deep eutectic solvent (DES) is studied. The synthesized DES is composed of 1:2 mole ratio of choline chloride and glycerol and is further characterized by Fourier transform infrared (FTIR) and ~(1)H NMR spectroscopy techniques. The critical micellar concentration (CMC), micellar size, and intermolecular interaction in surfactants within Gly-based DES solutions are investigated by various techniques including surface tension, conductivity, fluorescence, dynamic light scattering (DLS), FTIR, ~(1)H NMR, and two-dimensional (2D) nuclear Overhauser effect spectroscopy (NOESY). The various interfacial properties and thermodynamic parameters are determined in the presence of 5 wt % glyceline (Gly)-based DES in an aqueous solution. The CMC, aggregation number (N _(agg)), and Stern–Volmer constant (K _(sv)) have also been determined by a steady-state fluorescence method. DLS is used to obtain information regarding the size of the aggregates formed by the cationic surfactants in DES solutions. FTIR spectroscopy is used to study the surfactant–DES interactions that tune the micellar structure of the surfactants within the Gly-based DES solution. The functional groups involved in the interactions (H-bonding and electrostatic) are the head groups (HO–CH_(2)–CH_(2)–N~(+) ion for CDMEAB and quaternary phosphonium (P~(+)) ion for CTBPB) of the surfactants with the ?OH-containing Gly DES. The hydrophobic moieties are involved in the hydrophobic interactions. The ~(1)H NMR data show that differences in chemical shifts can provide significant information about the interactions taking place within the system. ~(1)H NMR and NOESY techniques are further employed to strengthen our claim on the feasible structural arrangements within the aqueous surfactant–DES self-assembled structures. It is observed that both the cationic surfactants, i.e., CDMEAB and CTBPB, form self-assembled nanostructures in the Gly-based DES solutions. The present results are expected to be useful for colloidal solutions of DES and their mixtures with water.
机译:研究了两种阳离子表面活性剂的聚集行为,即CyetyLdimethylylamon溴化铵(CDMEAB)和十六氧基膦鏻(CTBPB),在水性深海共晶溶剂(DES)中。合成的DES由1:2摩尔氯化胆碱和甘油的摩尔比组成,并进一步表征傅里叶变换红外(FTIR)和〜(1)H NMR光谱技术。通过包括表面张力,导电性,荧光,动态光散射(DLS),FTIR,〜(1)H NMR的各种技术研究了聚乙烯基DES溶液中的表面活性剂中的临界胶束浓度(CMC),胶束尺寸和分子间相互作用。 ,二维(2D)核传播效应光谱(NOESY)。各种界面性质和热力学参数在水溶液中存在5wt%的甘油精(Gly)的基础酸溶液中。 CMC,聚合号( N _(AGG))和泰铢常数( k _(SV))也通过稳态荧光法决定。 DLS用于获得关于由DES溶液中的阳离子表面活性剂形成的聚集体尺寸的信息。 FTIR光谱学用于研究表面活性剂-SES相互作用,其曲调基于GLY的DES溶液内表面活性剂的胶束结构。涉及相互作用(H键合和静电)的官能团是用于CDMEAB和季鏻的头部基团(HO-CH_(2)-CH_(2)-N〜(+)离子(P〜(+))离子对于含αOH的GLY DES的表面活性剂的CTBPB)。疏水性部分参与疏水相互作用。 〜(1)H NMR数据显示化学位移的差异可以提供有关系统内发生的相互作用的重要信息。 〜(1)H NMR和NOESY技术进一步用于加强我们对水性表面活性剂 - DES自组装结构中可行的结构布置的要求。观察到阳离子表面活性剂,即CdmeAb和CTBPB,在基于GLY的DES溶液中形成自组装的纳米结构。预计目前的结果将可用于DES及其混合物用水的胶体溶液有用。

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