Synthesis and application of dual‐layer metal‐organic framework as a fiber coating based on copper‐based metal‐organic framework @ zeolitic imidazolate framework‐8 for solid‐phase microextraction of some selected parabens and their quantification using high performance liquid chromatography

IF 1.3 Q4 CHEMISTRY, ANALYTICAL SEPARATION SCIENCE PLUS Pub Date : 2023-10-05 DOI:10.1002/sscp.202300141
Abeer Fadhil Mohammed, Milad Ghani, Jahan Bakhsh Raoof
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Abstract

Abstract Herein, the zeolitic imidazolate framework‐8 template was accommodated onto the surface of a pencil graphite substrate through the electrodeposition system. Then, Zn in the zeolitic imidazolate framework‐8 was replaced with Cu atoms via the galvanic replacement procedure. The modified template was used for the synthesis of another metal‐organic framework (copper‐benzene di carboxylic acid) by a solvothermal method. The prepared fiber was characterized by field emission‐scanning electron microscopy, Fourier transform infrared spectroscopy, and X‐ray diffraction technique. Then, it was employed for direct immersion solid‐phase microextraction of methyl, ethyl, and butyl parabens. Various factors, such as the pH of the sample solution, stirring rate, desorption volume, the concentration of salt, extraction time, and desorption time, were selected and optimized. Under the optimized condition (extraction time = 30 min, desorption time = 2 min, desorption volume = 200 μL, salt concentration = 0% w/v, sample solution pH = 3.0, and stirring rate = 700 rpm), the linearity of the method was in the range of 1–200 μg/L ( r 2 > 0.9926). The limits of detection and quantification fall between 0.28–0.65 μg/L and 0.91–1.98 μg/L, respectively. The analysis of selected parabens in toothpaste and hand and face lotion, were also done using the suggested methodology.
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基于铜基金属-有机骨架@沸石咪唑酯骨架- 8的双层金属-有机骨架纤维涂层的合成和应用,用于固相微萃取某些对羟基苯甲酸酯及其高效液相色谱定量分析
本文通过电沉积系统将沸石咪唑酸盐框架- 8模板安置在铅笔石墨衬底表面。然后,通过电替换程序将沸石咪唑盐框架- 8中的Zn替换为Cu原子。采用溶剂热法制备了另一种金属-有机骨架(铜-苯二羧酸)。利用场发射扫描电子显微镜、傅里叶变换红外光谱和X射线衍射技术对所制备的纤维进行了表征。然后,采用直接浸渍固相微萃取法提取对羟基苯甲酸甲酯、乙酯和丁酯。对样品溶液的pH、搅拌速率、解吸体积、盐浓度、萃取时间、解吸时间等因素进行了筛选和优化。在最佳提取时间为30 min,解吸时间为2 min,解吸体积为200 μL,盐浓度为0% w/v,样品溶液pH = 3.0,搅拌速度为700 rpm的条件下,该方法的线性范围为1 ~ 200 μg/L (r 2 >0.9926)。检测限为0.28 ~ 0.65 μg/L,定量限为0.91 ~ 1.98 μg/L。采用建议的方法对牙膏、洗手液和洗面乳中所选的对羟基苯甲酸酯进行了分析。
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来源期刊
SEPARATION SCIENCE PLUS
SEPARATION SCIENCE PLUS CHEMISTRY, ANALYTICAL-
CiteScore
1.90
自引率
9.10%
发文量
111
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