{"title":"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","authors":"Abeer Fadhil Mohammed, Milad Ghani, Jahan Bakhsh Raoof","doi":"10.1002/sscp.202300141","DOIUrl":null,"url":null,"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.","PeriodicalId":21639,"journal":{"name":"SEPARATION SCIENCE PLUS","volume":"124 1","pages":"0"},"PeriodicalIF":1.3000,"publicationDate":"2023-10-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"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\",\"authors\":\"Abeer Fadhil Mohammed, Milad Ghani, Jahan Bakhsh Raoof\",\"doi\":\"10.1002/sscp.202300141\",\"DOIUrl\":null,\"url\":null,\"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.\",\"PeriodicalId\":21639,\"journal\":{\"name\":\"SEPARATION SCIENCE PLUS\",\"volume\":\"124 1\",\"pages\":\"0\"},\"PeriodicalIF\":1.3000,\"publicationDate\":\"2023-10-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"SEPARATION SCIENCE PLUS\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/sscp.202300141\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"SEPARATION SCIENCE PLUS","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/sscp.202300141","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
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
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.