基于真空辅助顶空固相微萃取的土壤水提物中不对称二甲肼转化产物的定量研究

IF 0.3 Q4 CHEMISTRY, MULTIDISCIPLINARY Chemical Bulletin of Kazakh National University Pub Date : 2018-06-30 DOI:10.15328/CB1014
D. Orazbayeva, B. Kenessov, A. Zhakupbekova
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引用次数: 6

摘要

土壤中偏二甲肼(UDMH)转化产物的定量需要繁琐、耗时和费力的样品制备。本工作优化了真空辅助顶空固相微萃取(Vac-HSPME)测定土壤水提取物中UDMH转化产物的简单快速方法。该方法基于用水从土壤中提取分析物,然后对所获得的水提取物进行Vac HSSPME,以及气相色谱-质谱分析。目标转化产物为:吡嗪、1-甲基-1H-吡唑、N-亚硝基二甲胺、N,N-二甲基甲酰胺、1-甲基-1Н-1,2,4-三唑、1-甲基咪唑和1H-吡唑。研究了样品pH对目标分析物响应的影响。它可以忽略不计,并且在随后的提取之前不建议调节pH。对水量进行了优化,以提供分析物响应及其精度的最佳组合。通过向2.0g土壤中加入7.00mL水进行提取,确保了分析物的响应与其在土壤中的浓度的线性相关性。优化的方法提供了土壤中目标分析物的检测限在0.2至9ng/g范围内。模型样品的尖峰回收率在90-103%的范围内。所开发的方法可推荐应用于实验室,对可能被火箭燃料残留物污染的土壤样本进行常规分析。
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Quantification of transformation products of unsymmetrical dimethylhydrazine in aqueous extracts from soil based on vacuum-assisted headspace solid-phase microextraction
Quantification of transformation products of unsymmetrical dimethylhydrazine (UDMH) in soil requires tedious, time- and labor-consuming sample preparation. The simple and fast method for quantification of transformation products of UDMH in aqueous extracts from soil using vacuum-assisted headspace solid-phase microextraction (Vac-HSSPME) was optimized in this work. The method is based on extraction of analytes from soil with water followed by Vac-HSSPME of the obtained aqueous extracts, and gas chromatography-mass spectrometry analysis. The target transformation products were: pyrazine, 1-methyl-1H-pyrazole, N-nitrosodimethylamine, N,N-dimethylformamide, 1-methyl-1Н-1,2,4-triazole, 1-methyl-imidazole and 1H-pyrazole. The effect of a sample pH on responses of target analytes was studied. It was negligible, and no pH adjustment was recommended before a subsequent extraction. The water amount was optimized to provide the best combination of analytes responses and their precision. Extraction by adding 7.00 mL of water to 2.0 g of soil ensured linear dependence of responses of the analytes on their concentrations in soil. The optimized method provided detection limits of target analytes in soil in the range from 0.2 to 9 ng/g. The spike recoveries obtained for model samples were in the range 90-103%. The developed method can be recommended for application in laboratories conducting routine analyses of soil samples potentially contaminated by rocket fuel residuals.
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