{"title":"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","authors":"D. Orazbayeva, B. Kenessov, A. Zhakupbekova","doi":"10.15328/CB1014","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":9860,"journal":{"name":"Chemical Bulletin of Kazakh National University","volume":null,"pages":null},"PeriodicalIF":0.3000,"publicationDate":"2018-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":"{\"title\":\"Quantification of transformation products of unsymmetrical dimethylhydrazine in aqueous extracts from soil\\nbased on vacuum-assisted headspace solid-phase microextraction\",\"authors\":\"D. Orazbayeva, B. Kenessov, A. Zhakupbekova\",\"doi\":\"10.15328/CB1014\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"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.\",\"PeriodicalId\":9860,\"journal\":{\"name\":\"Chemical Bulletin of Kazakh National University\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.3000,\"publicationDate\":\"2018-06-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Bulletin of Kazakh National University\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15328/CB1014\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Bulletin of Kazakh National University","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15328/CB1014","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
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.