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Neutral monolithic capillary columns with alkyl and aryl ligands for reversed-phase capillary electrochromatography.

机译:具有烷基和芳基配体的中性整体毛细管柱,用于反相毛细管电色谱。

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摘要

Scope and Method of Study. The broad objective of this dissertation involved an integrated approach for furthering the advancement of reversed-phase capillary electrochromatography (RP-CEC) by providing an improved design of neutral acrylate/methacrylate--based monoliths offering both hydrophobic and pi interactions for separating a wide range of solutes including polyionic biomolecules such as peptides and proteins. Being neutral, the monoliths were void of fixed charges that are traditionally incorporated to support EOF but still afforded relatively strong electrosomotic flow (EOF) necessary for mass transport in the absence of annoying electrostatic interactions. Such interactions would otherwise lead to irreversible adsorption of charged analytes to the stationary phase surface, causing band broadening and irreproducible retention times. Towards this end, octadecyl acrylate monoliths (ODM), naphthyl methacrylate monoliths (NMM), segmented monolithic columns (SMC) and mixed ligand monoliths (MLM) were developed and evaluated.Findings and Conclusions. The investigation described in this dissertation has significantly contributed to enhancing the scope of RP-CEC by demonstrating its capabilities in areas that had not been largely exploited previously. Although without fixed charges, the neutral monoliths afforded relatively strong EOF through the adsorption of ions from the electrolyte, which imparted the monolith with a given zeta potential to generate the EOF necessary for mass transport. The ODM columns provided hydrophobic interactions while the naphthyl methacrylate columns exhibited both hydrophobic and pi interactions. By changing the choice of the crosslinker, the EOF, retention and selectivity of the ODM and NMM were tuned. Similarly, the preparation of SMC and MLM provided a convenient way of tuning the magnitude of EOF, retention and selectivity towards both neutral and charged solutes. The novel stationary phases developed within the framework of this investigation will not only facilitate a solution to many separation problems in life sciences, but also contribute to new concepts that will broaden the utility of RP-CEC in the future.
机译:研究范围和方法。本论文的广泛目标涉及通过提供改进的中性丙烯酸酯/甲基丙烯酸酯基整体设计来改进反相毛细管电色谱(RP-CEC)的集成方法,该中性丙烯酸酯/甲基丙烯酸酯基团提供疏水和π相互作用以分离大范围溶质,包括聚离子生物分子,例如肽和蛋白质。由于是中性的,整料没有固定电荷,该固定电荷通常用于支持EOF,但在没有烦人的静电相互作用的情况下,仍提供了质量传输所需的相对较强的电渗流(EOF)。否则,此类相互作用将导致带电分析物不可逆地吸附到固定相表面,从而导致谱带展宽和不可再现的保留时间。为此,开发并评估了丙烯酸十八烷基酯(ODM),甲基丙烯酸萘酯(NMM),分段整体柱(SMC)和混合配体整体(MLM)。发现和结论。本文所描述的研究通过证明其在以前未曾被大量开发的领域中的能力,为扩大RP-CEC的范围做出了重大贡献。尽管没有固定电荷,但中性整料通过从电解质中吸收离子而提供了相对较强的EOF,这使整料具有给定的zeta电位,从而产生了质量传输所需的EOF。 ODM色谱柱提供了疏水相互作用,而甲基丙烯酸萘酯色谱柱则同时显示了疏水和pi相互作用。通过改变交联剂的选择,可以调整ODM和NMM的EOF,保留率和选择性。同样,SMC和MLM的制备为调节EOF的大小,保留性和对中性和带电溶质的选择性提供了便捷的方法。在此研究框架内开发的新的固定相不仅将有助于解决生命科学中的许多分离问题,而且还将为新概念做出贡献,这些新概念将在将来扩展RP-CEC的用途。

著录项

  • 作者

    Karenga, Samuel Mukiha.;

  • 作者单位

    Oklahoma State University.;

  • 授予单位 Oklahoma State University.;
  • 学科 Chemistry Analytical.Chemistry Polymer.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 215 p.
  • 总页数 215
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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