首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Novel amphiphilic polymeric ionic liquid-solid phase micro-extraction membrane for the preconcentration of aniline as degradation product of azo dye Orange G under sonication by liquid chromatography–tandem mass spectrometry
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Novel amphiphilic polymeric ionic liquid-solid phase micro-extraction membrane for the preconcentration of aniline as degradation product of azo dye Orange G under sonication by liquid chromatography–tandem mass spectrometry

机译:液相色谱-串联质谱法超声处理用于偶氮染料Orange G降解产物苯胺预浓缩的新型两亲高分子离子液体固相微萃取膜

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摘要

A novel amphiphilic polymeric ionic liquid membrane containing a hydrophilic bromide anion and a hydrophobic carbonyl group was synthesized in dimethylformamide (DMF) systems using the ionic liquid 1-butyl-3-vinylimidazolium bromide (BVImBr) and the methylmethacrylate (MMA) as monomers. The prepared amphiphilic ploy-methylmethacrylate-1-butyl-3-vinylimidazolium bromide (MMA-BVImBr) was characterized by a scanning electron microscope and an infrared spectrum instrument. The results of solid-phase micro-extraction membrane (SPMM) experiments showed that the adsorption capacity of membrane was about 0.76 μg μg~(?1) for aniline. Based on this, a sensitive method for the determination of trace aniline, as a degradation product of azo dye Orange G under sonication, was developed by liquid chromatography–tandem mass spectrometry (LC–MS/MS). The calibration curve showed a good linearity ranging from 0.5 to 10.0 μg L~(?1) with a correlation coefficient value of 0.9998. The limit of quantification was 0.5 μg L~(?1). The recoveries ranged from 90.6% to 96.1%. The intra- and inter-day relative standard deviations were less than 8.3% and 10.9%. The developed SPMM-LC–MS/MS method was used successfully for preconcentration of trace aniline produced during the sonication of Orange G solution.
机译:以离子液体溴化1-丁基-3-乙烯基咪唑鎓(BVImBr)和甲基丙烯酸甲酯(MMA)为单体,在二甲基甲酰胺(DMF)系统中合成了一种新型的两亲性聚合物离子液体膜,该膜包含亲水性溴阴离子和疏水性羰基。通过扫描电子显微镜和红外光谱仪对制得的两亲性聚甲基丙烯酸甲酯-1-丁基-3-乙烯基咪唑鎓溴化物(MMA-BVImBr)进行表征。固相微萃取膜(SPMM)实验结果表明,该膜对苯胺的吸附能力约为0.76μgμg〜(?1)。在此基础上,通过液相色谱-串联质谱法(LC-MS / MS)建立了一种灵敏的测定痕量苯胺的方法,痕量苯胺是偶氮染料Orange G在超声处理下的降解产物。校准曲线显示出良好的线性,范围为0.5至10.0μgL〜(?1),相关系数值为0.9998。定量限为0.5μgL〜(?1)。回收率从90.6%到96.1%。日内和日间相对标准偏差分别小于8.3%和10.9%。发达的SPMM-LC-MS / MS方法已成功用于橙汁G溶液超声处理过程中产生的痕量苯胺的预浓缩。

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