Caglayan Berna, Unsal Ender, Camli S Tolga, Tuncel Murvet, Tuncel Ali
Hacettepe University, Faculty of Engineering, Chemical Engineering Department, Ankara, Turkey.
J Sep Sci. 2006 May;29(7):936-44. doi: 10.1002/jssc.200500499.
A single-stage swelling and polymerization method was proposed for the synthesis of monodisperse porous poly(vinyl acetate-co-divinylbenzene) [poly(VAc-co-DVB)] particles with different VAc/DVB feed ratios. The particles obtained with the VAc/DVB feed ratio of 50:50 v/v had a narrow pore size distribution exhibiting a sharp peak at 30 nm. Based on this distribution the mean pore size and the specific volume were determined as 12 nm and 1.39 mL/g, respectively. The specific surface area of poly(VAc-co-DVB) particles was found to be 470 m2/g. These properties make poly(VAc-co-DVB) particles a promising support for potential HPLC applications. Poly(vinyl alcohol-co-divinylbenzene) [poly(VA-co-DVB)] particles were then obtained by the basic hydrolysis of poly(VAc-co-DVB) particles. The hydroxyl groups on poly(VA-co-DVB) particles have a suitably reactive functionality for surface grafting or derivatization protocols aiming at synthesizing various HPLC packings. The examination of poly(VA-co-DVB) particles by confocal laser scanning microscopy showed the homogeneous distribution of hydroxyl functionality in the particle interior. As a starting point, the chromatographic performance of plain material, poly(VAc-co-DVB) particles produced with VAc/DVB feed ratio of 50:50 (v/v) was tested by a commonly utilized chromatographic mode, reversed phase chromatography. Poly(VAc-co-DVB) particles were successfully used as packing material in the RP separation of alkylbenzenes with resolutions higher than 1.5. Theoretical plate numbers up to 17 500 plates/m were achieved. No significant change both in the chromatographic resolution and column efficiency was observed with increasing flow rate. The chromatography showed that poly(VAc-co-DVB) particles were a suitable starting material for the synthesis of chromatographic packings for different modes of HPLC.
提出了一种单步溶胀聚合方法,用于合成具有不同醋酸乙烯酯/二乙烯基苯(VAc/DVB)进料比的单分散多孔聚(醋酸乙烯酯 - 共 - 二乙烯基苯)[聚(VAc - 共 - DVB)]颗粒。VAc/DVB进料比为50:50 v/v时获得的颗粒具有窄的孔径分布,在30 nm处呈现尖锐峰。基于此分布,平均孔径和比容分别确定为12 nm和1.39 mL/g。聚(VAc - 共 - DVB)颗粒的比表面积为470 m²/g。这些特性使聚(VAc - 共 - DVB)颗粒成为潜在高效液相色谱(HPLC)应用的有前景的载体。然后通过聚(VAc - 共 - DVB)颗粒的碱性水解获得聚(乙烯醇 - 共 - 二乙烯基苯)[聚(VA - 共 - DVB)]颗粒。聚(VA - 共 - DVB)颗粒上的羟基具有适当的反应性功能,可用于旨在合成各种HPLC填料的表面接枝或衍生化方案。通过共聚焦激光扫描显微镜对聚(VA - 共 - DVB)颗粒的检查显示羟基官能团在颗粒内部均匀分布。作为起点,采用常用的色谱模式反相色谱法测试了VAc/DVB进料比为50:50(v/v)的普通材料聚(VAc - 共 - DVB)颗粒的色谱性能。聚(VAc - 共 - DVB)颗粒成功用作烷基苯RP分离的填充材料,分离度高于1.5。理论塔板数高达17500塔板/米。随着流速增加,色谱分辨率和柱效均未观察到显著变化。色谱分析表明,聚(VAc - 共 - DVB)颗粒是合成不同模式HPLC色谱填料的合适起始材料。