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Micellar liquid chromatography of polyaromatic hydrocarbons using anionic, cationic, and nonionic surfactants: Armstrong model, LSER interpretation

机译:使用阴离子,阳离子和非离子表面活性剂的聚芳烃的胶束液相色谱:Armstrong模型,LSER解释

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摘要

The capacity factorsk of 28 polycromatic hydrocarbons (PAHs) were determined by micellarliquid chromatography (CLM) in several mobiles phases containing anionic (SDS), cationic (CTAB), or non-ionic(Brij 35) surfactants. The micelle-water binding constantsK MW were calculated via the Armstrong theory. Linear solvation energy relationship (LSER) were used to correlatek andK MW with the PAHs solvatochromic descriptors. LSER correlation was convenient fork. were The most important factors appeared to be the size and basicity of the PAHs. In the retention of the PAHs, their volume interacted positively and their basicity negatively. LSER correlation ofK MW was relatively poor due to the difficult and complex transfer PAHs from water to the micelles. The volume and basicity strongly influenced theK MW, depending on the surfactant. With SDS or Brij 35, the PAH size increasedK MW whereas its basicity decreasedK MW. The opposite was observed with CTAB.
机译:通过胶束液相色谱(CLM)在含有阴离子(SDS),阳离子(CTAB)或非离子(Brij 35)表面活性剂的几种流动相中测定28种多沸碳氢化合物(PAH)的容量因子。利用阿姆斯特朗理论计算了胶束与水的结合常数K MW 。利用线性溶剂化能量关系(LSER)将PAHs和PAHs的溶剂化变色描述子与K MW 相关联。 LSER相关性很方便。最重要的因素似乎是多环芳烃的大小和碱性。在保留多环芳烃的过程中,它们的体积呈正相关,而其碱度呈负相关。由于PAHs从水到胶束的转移过程复杂而复杂,因此K MW的LSER相关性相对较差。取决于表面活性剂,其体积和碱度对K MW 有很大影响。使用SDS或Brij 35时,PAH的大小增加了K MW ,而其碱度却减小了K MW 。用CTAB观察到相反的情况。

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