Farajzadeh Mir Ali, Rahimzadeh Sakineh, Afshar Mogaddam Mohammad Reza, Bakhshizadeh Aghdam Mehri
Department of Analytical Chemistry, Faculty of Chemistry, University of Tabriz Tabriz Iran
Engineering Faculty, Near East University 99138 Nicosia Mersin 10 North Cyprus Turkey.
RSC Adv. 2024 Sep 3;14(38):28035-28043. doi: 10.1039/d4ra02795g. eCollection 2024 Aug 29.
In this work, Zn-1,4-benzenedicarboxylate metal-organic framework was synthesized by a simple hydrothermal process and used in dispersive micro solid phase extraction of some pesticide from various fruit juice and water samples. Seven widely consumed pesticides in agriculture (chlorpyrifos, haloxyfop--methyl, oxadiazon, diniconazole, clodinafop-propargyl, fenpropathrin, and fenaxoprop--ethyl) were selected as target analytes. In this work, dispersive micro solid phase extraction was followed by a liquid phase microextraction method to achieve more enrichment of the analytes, and the enriched analytes were quantified using a gas chromatography-flame ionization detector. The sorbent was authenticated by Fourier transform infrared spectrophotometry, X-ray diffraction, energy dispersive X-ray analysis, and scanning electron microscope imaging. The factors affecting the extraction efficiency of the developed method were investigated, and the validation of the method under the optimized extraction conditions presented satisfactory results for precision and trueness, with limits of detection and quantification in the ranges of 0.50-0.90 and 1.5-2.7 μg L, respectively. Enrichment factors and extraction recoveries were in the ranges of 239-392% and 47-78%, respectively. One river water and some fruit and vegetable juice samples were analyzed by the recommended method, and the obtained recoveries were between 90% and 102%.
在本研究中,通过简单的水热法合成了锌-1,4-苯二甲酸金属有机框架,并将其用于从各种果汁和水样中分散微固相萃取某些农药。选择了七种农业中广泛使用的农药(毒死蜱、高效氟吡甲禾灵、恶草酮、烯唑醇、炔草酸、甲氰菊酯和乙羧氟草醚)作为目标分析物。在本研究中,分散微固相萃取之后采用液相微萃取方法以实现分析物的更多富集,富集后的分析物使用气相色谱-火焰离子化检测器进行定量。通过傅里叶变换红外光谱、X射线衍射、能量色散X射线分析和扫描电子显微镜成像对吸附剂进行了鉴定。研究了影响所开发方法萃取效率的因素,在优化的萃取条件下对该方法进行验证,结果表明精密度和准确性令人满意,检测限和定量限分别在0.50 - 0.90和1.5 - 2.7 μg/L范围内。富集因子和萃取回收率分别在239 - 392%和47 - 78%范围内。采用推荐方法对一个河水样本以及一些果蔬汁样本进行了分析,获得的回收率在90%至102%之间。