{"title":"化学锚定在二氧化硅纳米颗粒上的酰胺基共价有机框架,用于空气中卤代烃的顶空微量萃取采样","authors":"","doi":"10.1016/j.chroma.2024.465387","DOIUrl":null,"url":null,"abstract":"<div><div>A needle trap device (NTD) was developed using an amide-based covalent-organic framework (COF), chemically bonded to silica nanoparticles. The NTD was coupled with gas chromatography-flame ionization detection (GC-FID) and employed for the headspace microextraction analysis of halogenated hydrocarbons (HHCs) in the air. The adsorbent was characterized using Fourier-transform infrared spectroscopy (FT-IR), X-ray diffraction analysis (XRD), transmission electron microscopy (TEM), and field-emission scanning electron microscopy (FE-SEM) techniques.</div><div>Optimal values for the experimental variables were assessed using response surface methodology (RSM) with a central composite design (CCD), thereby reducing the number of experiments, material consumption, costs, and time. The optimal values for desorption time and temperature were obtained 5 min and 260 °C, respectively. Breakthrough volume (BtV) was studied over the range of 0.5 - 3 times the occupational exposure limit (OEL) and its optimal value was found to be 1200 mL. The optimal sampling temperature and relative humidity (RH) were obtained 20 °C, and 15 %, respectively. The limits of detection (LODs) and limits of quantification (LOQs) were ranged from 0.013 to 0.077 μg <span>l</span><sup>-1</sup> and 0.041 to 0.21 μg <span>l</span><sup>-1</sup>, respectively, with a linear dynamic range (LDR) of 0.04 to 100 μg <span>l</span><sup>-1</sup>. The method's repeatability and reproducibility (RSD %) were observed over the ranges of 5.3 - 6.4 % and 4.7 -6.9 %, respectively. A statistically validated agreement was observed between the NTD-GC-FID method and the NIOSH 1003 standard procedure for the sampling and determination of HHCs in real workplace air samples, demonstrating the reliability and accuracy of the developed approach.</div></div>","PeriodicalId":347,"journal":{"name":"Journal of Chromatography A","volume":null,"pages":null},"PeriodicalIF":3.8000,"publicationDate":"2024-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"An amide-based covalent organic framework chemically anchored on silica nanoparticles for headspace microextraction sampling of halogenated hydrocarbons in air\",\"authors\":\"\",\"doi\":\"10.1016/j.chroma.2024.465387\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A needle trap device (NTD) was developed using an amide-based covalent-organic framework (COF), chemically bonded to silica nanoparticles. The NTD was coupled with gas chromatography-flame ionization detection (GC-FID) and employed for the headspace microextraction analysis of halogenated hydrocarbons (HHCs) in the air. The adsorbent was characterized using Fourier-transform infrared spectroscopy (FT-IR), X-ray diffraction analysis (XRD), transmission electron microscopy (TEM), and field-emission scanning electron microscopy (FE-SEM) techniques.</div><div>Optimal values for the experimental variables were assessed using response surface methodology (RSM) with a central composite design (CCD), thereby reducing the number of experiments, material consumption, costs, and time. The optimal values for desorption time and temperature were obtained 5 min and 260 °C, respectively. Breakthrough volume (BtV) was studied over the range of 0.5 - 3 times the occupational exposure limit (OEL) and its optimal value was found to be 1200 mL. The optimal sampling temperature and relative humidity (RH) were obtained 20 °C, and 15 %, respectively. The limits of detection (LODs) and limits of quantification (LOQs) were ranged from 0.013 to 0.077 μg <span>l</span><sup>-1</sup> and 0.041 to 0.21 μg <span>l</span><sup>-1</sup>, respectively, with a linear dynamic range (LDR) of 0.04 to 100 μg <span>l</span><sup>-1</sup>. The method's repeatability and reproducibility (RSD %) were observed over the ranges of 5.3 - 6.4 % and 4.7 -6.9 %, respectively. A statistically validated agreement was observed between the NTD-GC-FID method and the NIOSH 1003 standard procedure for the sampling and determination of HHCs in real workplace air samples, demonstrating the reliability and accuracy of the developed approach.</div></div>\",\"PeriodicalId\":347,\"journal\":{\"name\":\"Journal of Chromatography A\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2024-09-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Chromatography A\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0021967324007611\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chromatography A","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0021967324007611","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
An amide-based covalent organic framework chemically anchored on silica nanoparticles for headspace microextraction sampling of halogenated hydrocarbons in air
A needle trap device (NTD) was developed using an amide-based covalent-organic framework (COF), chemically bonded to silica nanoparticles. The NTD was coupled with gas chromatography-flame ionization detection (GC-FID) and employed for the headspace microextraction analysis of halogenated hydrocarbons (HHCs) in the air. The adsorbent was characterized using Fourier-transform infrared spectroscopy (FT-IR), X-ray diffraction analysis (XRD), transmission electron microscopy (TEM), and field-emission scanning electron microscopy (FE-SEM) techniques.
Optimal values for the experimental variables were assessed using response surface methodology (RSM) with a central composite design (CCD), thereby reducing the number of experiments, material consumption, costs, and time. The optimal values for desorption time and temperature were obtained 5 min and 260 °C, respectively. Breakthrough volume (BtV) was studied over the range of 0.5 - 3 times the occupational exposure limit (OEL) and its optimal value was found to be 1200 mL. The optimal sampling temperature and relative humidity (RH) were obtained 20 °C, and 15 %, respectively. The limits of detection (LODs) and limits of quantification (LOQs) were ranged from 0.013 to 0.077 μg l-1 and 0.041 to 0.21 μg l-1, respectively, with a linear dynamic range (LDR) of 0.04 to 100 μg l-1. The method's repeatability and reproducibility (RSD %) were observed over the ranges of 5.3 - 6.4 % and 4.7 -6.9 %, respectively. A statistically validated agreement was observed between the NTD-GC-FID method and the NIOSH 1003 standard procedure for the sampling and determination of HHCs in real workplace air samples, demonstrating the reliability and accuracy of the developed approach.
期刊介绍:
The Journal of Chromatography A provides a forum for the publication of original research and critical reviews on all aspects of fundamental and applied separation science. The scope of the journal includes chromatography and related techniques, electromigration techniques (e.g. electrophoresis, electrochromatography), hyphenated and other multi-dimensional techniques, sample preparation, and detection methods such as mass spectrometry. Contributions consist mainly of research papers dealing with the theory of separation methods, instrumental developments and analytical and preparative applications of general interest.