Department of Analytical Chemistry and Organic Chemistry, Universitat Rovira I Virgili, Sescelades Campus, Marcel•lí Domingo s/n, 43007 Tarragona, Spain.
WestCHEM, Department of Pure and Applied Chemistry, University of Strathclyde, Thomas Graham Building, 295 Cathedral Street, Glasgow, G1 1XL, Scotland, United Kingdom.
J Chromatogr A. 2020 Aug 30;1626:461348. doi: 10.1016/j.chroma.2020.461348. Epub 2020 Jun 16.
Solid-phase extraction (SPE) is a widely-used and very well-established sample preparation technique for liquid samples. An area of on-going focus for innovation in this field concerns the development of new and improved SPE sorbents that can enhance the sensitivity and/or the selectivity of SPE processes. In this context, mixed-mode ion-exchange sorbents have been developed and commercialised, thereby allowing enhanced capacity and selectivity to be offered by one single material. The ion-selectivity of these materials is such that either anion-exchange or cation-exchange is possible, however one limitation to their use is that more than one sorbent type is required to capture both anions and cations. In this paper, we disclose the design, synthesis and exploitation of a novel SPE sorbent based on microporous polymer microspheres with amphoteric character. We show that it is possible to switch the ion-exchange retention mechanism of the sorbent simply by changing the pH of the loading solution; anion-exchange dominates at low pH, cation-exchange dominates at high pH, and both mechanisms can contribute to retention when the polymer-bound amphoteric species, which are based on the α-amino acid sarcosine (N-methylglycine), are in a zwitterionic state. This is an interesting and useful feature, since it allows distinctly different groups of analytes (acids and bases) to be fractionated using one single amphoteric sorbent with dual-functionality. The sarcosine-based sorbent was applied to the SPE of acidic, basic and amphoteric analytes from ultrapure water, river water and effluent wastewater samples. Under optimised conditions (loading 100 mL of sample at pH 6, washing with 1 mL of MeOH and eluting with an acidic or basic additive in MeOH) the recoveries for most of the compounds were from 57% to 87% for river water and from 61% to 88% for effluent wastewater. We anticipate that these results will lay the basis for the development of a new family of multifunctional sorbents, where two or more separation mechanisms can be embedded within one single, bespoke material optimised for application to challenging chemical separations to give significant selectivity advantages over essentially all other state-of-the-art SPE sorbents.
固相萃取(SPE)是一种广泛使用且非常成熟的液体样品制备技术。该领域持续关注的创新领域之一是开发新型和改进的 SPE 吸附剂,以提高 SPE 过程的灵敏度和/或选择性。在这种情况下,混合模式离子交换吸附剂已经开发并商业化,从而使一种单一材料能够提供增强的容量和选择性。这些材料的离子选择性使得可以进行阴离子交换或阳离子交换,但是它们的使用存在一个限制,即需要不止一种吸附剂类型才能同时捕获阴离子和阳离子。在本文中,我们披露了一种基于具有两性特征的微孔聚合物微球的新型 SPE 吸附剂的设计、合成和应用。我们表明,通过简单地改变加载溶液的 pH 值,就可以改变吸附剂的离子交换保留机制;在低 pH 值下,阴离子交换占主导地位,在高 pH 值下,阳离子交换占主导地位,当基于 α-氨基酸肌氨酸(N-甲基甘氨酸)的聚合物结合两性物质处于两性离子状态时,两种机制都可以有助于保留。这是一个有趣且有用的特点,因为它允许使用一种具有双重功能的单一两性吸附剂对明显不同的分析物组(酸和碱)进行分离。基于肌氨酸的吸附剂被应用于超纯水、河水和废水样品中酸性、碱性和两性分析物的 SPE。在优化条件下(在 pH 6 下加载 100 mL 样品,用 1 mL MeOH 洗涤,用 MeOH 中的酸性或碱性添加剂洗脱),大多数化合物在河水中的回收率为 57%至 87%,在废水中的回收率为 61%至 88%。我们预计,这些结果将为新型多功能吸附剂的开发奠定基础,其中可以在一种单一的、定制的材料中嵌入两种或更多种分离机制,该材料针对具有挑战性的化学分离进行优化,与基本上所有其他最先进的 SPE 吸附剂相比,具有显著的选择性优势。