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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Preparation of polymer monolithic column functionalized by arsonic acid groups for mixed-mode capillary liquid chromatography
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Preparation of polymer monolithic column functionalized by arsonic acid groups for mixed-mode capillary liquid chromatography

机译:用芳酮型毛细管液相色谱法制备聚合物整体柱的制备

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A mixed-mode polymer monolithic column functionalized by arsonic acid groups was prepared by single-step in situ copolymerization of monomers p-methacryloylaminophenylarsonic acid (p-MAPHA) and pentaerythritol triacrylate (PETA). The prepared poly(p-MAPHA-co-PETA) monolithic column has a homogeneous monolithic structure with good permeability and mechanical stability. Zeta potential measurements reveal that the monolithic stationary phase holds a negative surface charge when the mobile phase resides in the pH range of 3.0-8.0. The retention mechanisms of prepared monolithic column are explored by the separation of selected polycyclic aromatic hydrocarbons (PAHs), nucleosides, and three basic compounds. The results indicate that the column functions in three different separation modes associated with reversed-phase chromatography based on hydrophobic interaction, hydrophilic interaction chromatography, and cation-exchange chromatography. The column efficiency of prepared monolithic column is estimated to be 70,000 and 76,000 theoretical plates/in for thiourea and naphthalene, respectively, at a linear flow velocity of 0.85 mm/s using acetonitrile/H2O (85/15, v/v) as the mobile phase. Furthermore, an analysis of the retention factors obtained for the PAHs indicates that the prepared monolithic column exhibits good reproducibility with relative standard deviations of 2.9%, 4.0%, and 4.7% based on run-to-run injections, column-to-column preparation, and batch-to-batch preparation, respectively. Finally, we investigate the separation performance of the proposed monolithic column for select phenols, sulfonamides, nucleobases and nucleosides. (C) 2018 Elsevier B.V. All rights reserved.
机译:通过单体对单体对甲基丙烯酰基脲烯烯基(P-MAPHA)和季戊四醇三丙烯酸甲酸(PETA)的单步合并制备由芳官酸基团官能化的混合模式聚合物整体柱。制备的聚(P-Mapha-Co-PETA)整体柱具有良好渗透性和机械稳定性的均匀整体结构。 Zeta电位测量表明,当移动相位在3.0-8.0的pH范围内时,整体静止相保持负面电荷。通过分离所选多环芳烃(PAHS),核苷和三种碱性化合物,探索制备单片柱的保留机制。结果表明,基于疏水性相互作用,亲水相互作用色谱和阳离子交换色谱法,柱用三种不同的分离模式起作用。制备的整体柱的柱效率分别估计为70,000和76,000个用于硫脲和萘,在使用乙腈/ H2O(85/15,v / v)的线性流速为0.85mm / s的萘和萘。流动阶段。此外,对PAHS获得的保留因子的分析表明,基于跑步喷射的柱状制剂,制备的整体柱具有良好的2.9%,4.0%和4.7%的相对标准偏差和分批的批量备制备。最后,我们研究了所提出的单片柱的分离性能,用于选择酚,磺酰胺,核碱基和核苷。 (c)2018年elestvier b.v.保留所有权利。

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