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首页> 外文期刊>Journal of the Iranian Chemical Society >Fast dispersive liquid-liquid microextraction based on magnetic retrieval of in situ formed an ionic liquid for the preconcentration and determination of benzophenone-type UV filters from environmental water samples
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Fast dispersive liquid-liquid microextraction based on magnetic retrieval of in situ formed an ionic liquid for the preconcentration and determination of benzophenone-type UV filters from environmental water samples

机译:基于原位磁检索的快速分散液 - 液体微萃取形成了来自环境水样中的前浓缩的离子液体,并测定了苯酮型UV过滤器

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摘要

This work concerns the development of a novel and rapid in situ dispersive liquid-liquid microextraction method for magnetic retrieval of ionic liquid as a new approach for the separation of benzophenone type (BP-type) UV filters via quantification using UPLC with PDA detection. The analytes determined in this study were a group of three benzophenones: 2,4-dihydroxybenzophenone (BP1), 2,2',4,4'-tetrahydroxybenzophenone (BP2) and 2-hydroxy-4-metoxybenzophenone (BP3). The hydrophilic ionic liquid found suitable for use as an extraction solvent of the targeted analytes was didecyldimethylammonium chlorate (DDAC). An anion exchanger, NaClO4 was added to promote a metathesis reaction and in situ formed the IL, [DDA][ClO4]. The experimental parameters such as the concentration of IL, the molar ratio of DDAC to NaClO4, amount of iron oxide added and volume of water sample were investigated and optimised using a step-by-step optimisation process. The optimum experimental parameters were as follows: 30 mL of sample volume, 1% concentration of DDAC, the molar ratio of DDAC to NaClO4-1:2, and 5 mg of Fe3O4 magnetic nanoparticles. The proposed extraction method is simple and requires no more than 5 min. The detection limit (LOD) obtained for target analytes ranged from 12.320.0 ngL(-1), while the correlation coefficient (r(2)) was from 0.9995 to 0.9999. Finally, the developed method was successfully applied to the determination of BP-type UV filters in environmental water samples, and satisfactory results were obtained.
机译:这项工作涉及开发一种新颖且快速地原位分散液 - 液微萃取方法,用于离子液体的磁性检索作为通过使用UPLC与PDA检测的量化通过定量分离二苯甲酮型(BP型)UV过滤器的新方法。本研究中确定的分析物是一组三种二苯甲酮:2,4-二羟基二苯酮(BP1),2,2',4,4'-四羟基苯苯酮(BP2)和2-羟基-4-二氧化二苯酮(BP3)。发现适合用作靶向分析物的萃取溶剂的亲水离子液体是DIOD二甲基铵(DDAC)。加入阴离子交换器NaClO4以促进复分解反应,原位形成IL,[DDA] [CLO4]。实验参数如IL的浓度,DDAC至NaClO4的摩尔比,加入的氧化铁量和水样的体积,并使用逐步的优化过程进行优化。最佳实验参数如下:30ml样品体积,1%浓度的DDAC,DDAC至NaClO 4-1:2和5mg Fe 3 O 4磁性纳米颗粒的摩尔比。所提出的提取方法简单,不需要超过5分钟。用于靶分析物所获得的检测限(LOD)范围为12.320.0 ngL(-1),而相关系数(R(2))为0.9995至0.9999。最后,已成功地应用于环境水样中的测定BP型UV过滤器,获得了令人满意的结果。

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