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Polymeric sulfated surfactants with varied hydrocarbon tail: I. Synthesis, characterization, and application in micellar electrokinetic chromatography

机译:具有多种烃尾的聚合硫酸盐表面活性剂:I.合成,表征和在胶束电动色谱中的应用

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The influence of surfactant hydrocarbon tail on the solute/pseudostationary phase interactions was examined. Four anionic sulfated surfactants with 8-, 9-, 10-, and 11 carbon chains having a polymerizable double bond at the end of the hydrocarbon chain were synthesized and characterized before and after polymerization. The critical micelle concentration (CIVIC), polarity, and aggregation number of the four sodium alkenyl sulfate (SAIS) surfactants were determined using fluorescence spectroscopy. The partial specific volume of the polymeric SAIS (poly-SAIS) surfactants was estimated by density measurements and capillary electrophoresis (CE) was employed for determination of methylene selectivity as well as for elution window. The CIVIC of the monomers of SAIS surfactants decrease with increase in chain length and correlated well when fluorescence method was compared to CE. The physicochemical properties (partial specific volume, methylene selectivity, electrophoretic mobility, and elution window) increased with an increase in chain length. However, no direct relationship was found between the aggregation number and the length of hydrophobic tail of poly-SAIS surfactants. These polymeric surfactants were then used as pseudostationary phases in micellar electrokinetic chromatography (MEKC) to study the retention behavior and selectivity factor of 36 benzene derivatives with different chemical characteristics. Although variation in chain length of the polymeric surfactants significantly affects the retention of nonhydrogen bonding (NHB) benzene derivatives, these effects were less pronounced for hydrogen bond acceptor (HBA) and hydrogen bond donor (HBD) benzene derivatives. Therefore, hydrophobicity of poly-SAIS surfactants was found to be a major driving force for retention of NHB derivatives. However, for several benzene derivatives (NHB, HBA, and HBD) significantly higher selectivity factor was observed with longest chain polymeric surfactant (e.g., poly(sodium 10-undecenyl sulfate), poly-SUS) compared to shorter chain polymeric surfactant (e.g., poly(sodium 7-octenyl sulfate), poly-SOcS). In addition, the effect of the surfactant hydrophobic chain was also found to have some impact on migration order of NHB, HBA, and HBD benzene derivatives. [References: 43]
机译:检查了表面活性剂烃尾对溶质/假平稳相相互作用的影响。合成了四种具有在烃链末端具有可聚合双键的8、9、10和11个碳链的阴离子硫酸化表面活性剂,并在聚合前后进行了表征。使用荧光光谱法测定了四种链烯基硫酸钠(SAIS)表面活性剂的临界胶束浓度(CIVIC),极性和聚集数。聚合物SAIS(poly-SAIS)表面活性剂的部分比容通过密度测量进行估算,毛细管电泳(CE)用于确定亚甲基选择性以及洗脱窗口。与荧光法相比,SAIS表面活性剂单体的CIVIC随着链长的增加而降低,并且相关性很好。物理化学性质(部分比容,亚甲基选择性,电泳迁移率和洗脱窗口)随链长的增加而增加。然而,在聚SAIS表面活性剂的聚集数和疏水尾的长度之间没有发现直接关系。然后将这些聚合物表面活性剂用作胶束电动色谱(MEKC)中的假平稳相,以研究36种具有不同化学特性的苯衍生物的保留行为和选择性因子。尽管聚合物表面活性剂链长的变化会显着影响非氢键(NHB)苯衍生物的保留,但对于氢键受体(HBA)和氢键供体(HBD)苯衍生物,这些作用不太明显。因此,发现聚SAIS表面活性剂的疏水性是保留NHB衍生物的主要驱动力。但是,与较短链的聚合物表面活性剂(例如,NH4,HBA和HBD)相比,最长的链状聚合物表面活性剂(例如,聚(10-十一碳烯基硫酸钠),聚SUS)观察到了更高的选择性因子。聚(7-辛烯基硫酸钠),poly-SOcS)。另外,还发现表面活性剂疏水链的作用对NHB,HBA和HBD苯衍生物的迁移顺序有一定影响。 [参考:43]

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