Department of Chemistry, Lorestan University, Khoramabad, Iran.
Anal Chim Acta. 2019 Nov 20;1083:119-129. doi: 10.1016/j.aca.2019.07.063. Epub 2019 Aug 1.
Polyaniline silica (Silica/PANI) organic-inorganic nanocomposite was synthesized by combining electrospinning and in-situ polymerization processes. This strategy prevented the aggregation of PANI during the polymerization and led to higher synthesis's yield and more uniformity of the produced composite. The structure and morphology of the nanocomposite was characterized using Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), and X-ray diffraction (XRD) techniques. The prepared nanocomposite was then packed inside a stain-steel needle and evaluated as a needle trap device (NTD), for simultaneous headspace extraction of polycyclic aromatic hydrocarbons (PAHs) and benzene, toluene, ethylbenzene, and xylenes (BTEX) in polluted soil samples, before GC-FID analysis, as a low-cost and robust detector. Response surface methodology (RSM) involving Box-Behnken design (BBD) was implemented to evaluate the effective experimental variables and subsequent introduction of a multiple function to describe the experimental conditions for the extraction of the analytes. Wide calibration plots (1-2000 ng g for BTEX and 0.2-2000 ng g for PAHs) with acceptable linearity (R > 0.99) were obtained under the optimal conditions. The limits of detection were found to be 0.02-0.1 ng gfor BTEX and 0.001-0.01 ng g for PAHs. The calculated standard deviations were 7.3-13.2% (n = 6). The developed NTD-GC-FID method was successfully applied for the extraction and determination of PAHs and BTEX in contaminated soil samples.
聚苯胺二氧化硅(Silica/PANI)有机-无机纳米复合材料是通过结合静电纺丝和原位聚合工艺合成的。这种策略防止了 PANI 在聚合过程中的聚集,从而提高了合成的产率和所产生的复合材料的均匀性。使用傅里叶变换红外光谱(FT-IR)、扫描电子显微镜(SEM)和 X 射线衍射(XRD)技术对纳米复合材料的结构和形态进行了表征。然后,将制备的纳米复合材料装入不锈钢针中,并作为针捕集装置(NTD)进行评估,用于同时从污染土壤样品中提取多环芳烃(PAHs)和苯、甲苯、乙苯和二甲苯(BTEX),然后进行 GC-FID 分析,作为一种低成本且坚固的检测器。响应面法(RSM)涉及 Box-Behnken 设计(BBD)用于评估有效实验变量,并随后引入多函数来描述分析物提取的实验条件。在最佳条件下,获得了可接受线性度(R>0.99)的宽校准图(BTEX 为 1-2000ng g,PAHs 为 0.2-2000ng g)。发现 BTEX 的检测限为 0.02-0.1ng g,PAHs 的检测限为 0.001-0.01ng g。计算出的标准偏差为 7.3-13.2%(n=6)。所开发的 NTD-GC-FID 方法成功应用于污染土壤样品中 PAHs 和 BTEX 的提取和测定。