Department of Analytical Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz, Iran.
J Sep Sci. 2010 Jun;33(12):1816-28. doi: 10.1002/jssc.201000088.
Stir bar sorptive extraction (SBSE) combined with dispersive liquid-liquid microextraction (DLLME) has been developed as a new approach for the extraction of six triazole pesticides (penconazole, hexaconazole, diniconazole, tebuconazole, triticonazole and difenconazole) in aqueous samples prior to GC-flame ionization detection (GC-FID). A series of parameters that affect the performance of both steps were thoroughly investigated. Under optimized conditions, aqueous sample was stirred using a stir bar coated with octadecylsilane (ODS) and then target compounds on the sorbent (stir bar) were desorbed with methanol. The extract was mixed with 25 microL of 1,1,2,2-tetrachloroethane and the mixture was rapidly injected into sodium chloride solution 30% w/v. After centrifugation, an aliquot of the settled organic phase was analyzed by GC-FID. The methodology showed broad linear ranges for the six triazole pesticides studied, with correlation coefficients higher than 0.993, lower LODs and LOQs between 0.53-24.0 and 1.08-80.0 ng/mL, respectively, and suitable precision (RSD < 5.2%). Moreover, the developed methodology was applied for the determination of target analytes in several samples, including tap, river and well waters, wastewater (before and after purification), and grape and apple juices. Also, the presented SBSE-DLLME procedure followed by GC-MS determination was performed on purified wastewater. Penconazole, hexaconazole and diniconazole were detected in the purified wastewater that confirmed the obtained results by GC-FID determination. In short, by coupling SBSE with DLLME, advantages of two methods are combined to enhance the selectivity and sensitivity of the method. This method showed higher enrichment factors (282-1792) when compared with conventional methods of sample preparation to screen pesticides in aqueous samples.
搅拌棒吸附萃取(SBSE)结合分散液相微萃取(DLLME)已被开发为一种新方法,用于在 GC-火焰离子化检测(GC-FID)之前从水样中提取六种三唑类农药(丙环唑、己唑醇、烯唑醇、戊唑醇、三唑酮和氟环唑)。本文详细研究了影响两步萃取性能的一系列参数。在优化条件下,水样用十八烷基硅烷(ODS)涂覆的搅拌棒搅拌,然后用甲醇将目标化合物从吸附剂(搅拌棒)上解吸。萃取物与 25μL 1,1,2,2-四氯乙烷混合,然后将混合物迅速注入 30% w/v 的氯化钠溶液中。离心后,取有机相的一部分进行 GC-FID 分析。该方法对六种三唑类农药均具有较宽的线性范围,相关系数均高于 0.993,检出限和定量限分别为 0.53-24.0 和 1.08-80.0ng/mL,且精密度良好(RSD<5.2%)。此外,该方法还应用于多种水样中目标分析物的测定,包括自来水、河水和井水、废水(处理前后)以及葡萄汁和苹果汁。同时,还对净化后的废水进行了 GC-MS 测定,结果与 GC-FID 测定结果一致。在净化废水中检测到了丙环唑、己唑醇和烯唑醇,证实了 GC-FID 测定结果的准确性。总之,通过将 SBSE 与 DLLME 结合,将两种方法的优点结合起来,提高了方法的选择性和灵敏度。与传统的水样制备方法相比,该方法的富集因子(282-1792)更高,可用于筛选水样中的农药。