首页> 外文期刊>Analytical methods >Electrochemical preparation of a poly(aniline-co-m-aminobenzoic acid)-ionic liquid composite coating for the head-space solid phase microextraction and analysis of aryl halides
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Electrochemical preparation of a poly(aniline-co-m-aminobenzoic acid)-ionic liquid composite coating for the head-space solid phase microextraction and analysis of aryl halides

机译:顶空固相微萃取的聚苯胺-间-氨基-氨基苯甲酸-离子液体复合涂料的电化学制备及芳基卤化物的分析

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In this work, a novel poly(aniline-co-m-aminobenzoic acid)-ionic liquid composite coating is presented for the head-space solid phase microextraction (HS-SPME) of aryl halides (i.e. chlorobenzene, bromobenzene, 1,4-dichlorobenzene, 4-bromotoluene, and 1,2,4-trichlorobenzene). This coating was prepared on a platinum wire by electrochemical deposition in an aqueous solution containing 0.1 mol L-1 aniline, 0.1 mol L-1 m-aminobenzoic acid, 0.02 mol L-1 1-butyl-3-methylimidazolium tetrafluoroborate and 1.0 mol L-1 HNO3. It showed high mechanical stability, thermal stability (up to 320 degrees C) and durability (repetitively used for more than 120 times). When it was applied to the HS-SPME and gas chromatographic detection of aryl halides, it presented high repeatability and sensitivity. Under the optimized conditions (i.e. extraction temperature: 30 degrees C; extraction time: 30 min; stirring rate: 600 rpm; NaCl concentration: 0.35 g mL(-1)), the linear detection ranges were 0.2-100 mu g L-1 with correlation coefficients above 0.9922; the detection limits were 0.01-0.05 mu g L-1 (S/N = 3). The relative standard deviations (RSDs) of chromatographic peak areas were smaller than 5.3% for five successive measurements with a single fiber, and the fiber to fiber RSD was 2.4-9.5% (n = 3) for different aryl halides (50 mu g L-1). This method was successfully applied to the determination of real samples (i.e. moth balls) and the recoveries for the standard added were 85.7 % to 121%.
机译:在这项工作中,提出了一种新颖的聚(苯胺-间-氨基-氨基苯甲酸)-离子液体复合涂料,用于芳基卤化物(即氯苯,溴苯,1,4-)的顶空固相微萃取(HS-SPME)二氯苯,4-溴甲苯和1,2,4-三氯苯)。通过在包含0.1mol L-1苯胺,0.1mol L-1间氨基苯甲酸,0.02mol L-1 1-丁基-3-甲基咪唑四氟硼酸和1.0mol L的水溶液中电化学沉积在铂丝上制备该涂层。 -1 HNO3。它显示出很高的机械稳定性,热稳定性(高达320摄氏度)和耐久性(重复使用超过120次)。当将其用于HS-SPME和气相色谱法检测芳基卤化物时,它具有很高的重复性和灵敏度。在最佳条件下(即萃取温度:30℃;萃取时间:30分钟;搅拌速度:600 rpm; NaCl浓度:0.35 g mL(-1)),线性检测范围为0.2-100μgL-1相关系数高于0.9922;检出限为0.01-0.05μg L-1(S / N = 3)。使用单根光纤进行五次连续测量时,色谱峰面积的相对标准偏差(RSDs)小于5.3%,并且对于不同的芳基卤化物(50μg L,光纤到光纤的RSD为2.4-9.5%(n = 3)) -1)。该方法成功地用于测定真实样品(即飞蛾球),所添加标准品的回收率为85.7%至121%。

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