首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Determination of nitroaromatic, nitramine, and nitrate ester explosives in soil by gas chromatography and an electron capture detector
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Determination of nitroaromatic, nitramine, and nitrate ester explosives in soil by gas chromatography and an electron capture detector

机译:气相色谱法和电子捕获检测器测定土壤中的硝基芳香族,硝胺和硝酸酯类炸药

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摘要

Hazardous waste site characterization, forensic investigations, and land mine detection are scenarios where soils may be collected and analyzed for traces of nitroaromatic, nitramine, and nitrate ester explosives. These thermally labile analytes are traditionally determined by high-performance liquid chromatography (HPLC); however, commer-cially available deactivated injection port liners and wide-bore capillary columns have made routine analysis by gas chromatography (GC) possible. The electron-withdrawing nitro group common to each of these explosives makes the electron capture detector (ECD) suitable for determination of low concentrations of explosives in soil, water, and air. GC-ECD and HPLC-UV concentration estimates of explosives residues in field-contaminated soils from hazardous waste sites were compared, and correlation (r > 0.97) was excellent between the two methods of analysis for each of the compounds most frequently detected: 2,4,6-trinitrotoluene (TNT), hexahydro-l ,3,5-trinitro-l ,3,5-triazine (RDX), 2,4-dinitrotoluene (2,4-DNT), 1 ,3-dinitrobenzene (1 ,3-DNB), 1 ,3,5-trinitrobenzene (TNB), and octahydro-1 ,3,5,7-te-tranitro-l,3,5,7-tetrazocine (HMX). The analytes were extracted from soils with acetonitrile by 18 h of sonication in a cooled ultrasonic bath. Two soil-to-solvent ratios were evaluated: 2.00 g:l0.00 ml and 25.0 g:50.0 ml. GC-ECD method detection limits were similar for the two soil-to-solvent ratios and were about 1 jig kg — 1 for the di- and trinitroaromatics, about 10 jag kg 1 for the mono-nitroaromatics, 3 jag kg 1 for RDX, 25 jag kg 1 for HMX, and between 10 and 40 jig kg — for the nitrate esters (nitroglycerine [NG] and pentaerythritol tetranitrate [PETNI). Spike recovery studies revealed artifacts introduced by the spiking procedure. Recoveries were low in some soils if the amount of soil spiked was large (25.0 g) compared to the volume of spike solution added (1.00 ml). Recoveries were close to 100% when 2.00-g soil samples were spiked with 1.00 ml of solution. Analytes most frequently found in soils collected near buried land mines were the microbial transformation products of TNT (2-amino-4,6-dinitrotoluene [2-Am-DNT] and 4-amino-2,6-dinitrotoluene [4-Am-DNT]), manufacturing impurities of TNT (2,4-DNT, 2,6-DNT. and l,3-DNB), and TNT. The microbial reduction products of the isomers of DNT and of l,3-DNB were also detected, but the ECD response to these compounds is poor.
机译:危险废物现场表征,法医调查和地雷探测是可能会收集土壤并分析痕量硝基芳烃,硝胺和硝酸酯炸药的场景。这些热不稳定的分析物传统上是通过高效液相色谱法(HPLC)测定的。但是,市售的失活的进样口衬管和宽口径毛细管柱已使通过气相色谱(GC)进行常规分析成为可能。这些炸药中共有的吸电子硝基使电子捕获检测器(ECD)适用于测定土壤,水和空气中低浓度的炸药。比较了危险废物现场受田间污染的土壤中爆炸物残留的GC-ECD和HPLC-UV浓度估算值,对于两种最常检测到的化合物,两种分析方法之间的相关性(r> 0.97)极好:2 4,6-三硝基甲苯(TNT),六氢-1,3,5-三硝基-1,3,5-三嗪(RDX),2,4-二硝基甲苯(2,4-DNT),1,3-二硝基苯(1 ,3-DNB),1,3,5-三硝基苯(TNB)和八氢-1,3,5,7-四硝基-1,3,5,7-四唑啉(HMX)。通过在冷却的超声浴中超声处理18 h,用乙腈从土壤中提取分析物。评估了两种土壤与溶剂的比例:2.00 g:100.00 ml和25.0 g:50.0 ml。 GC-ECD方法对两种土壤与溶剂的比率的检测限相似,二硝基和三硝基芳烃的检出限约为1夹具公斤-1,一硝基硝基芳烃的检出限约为10公斤公斤1,RDX的检出限为3公斤公斤1, HMX为25千克kg 1,硝酸酯(硝酸甘油[NG]和季戊四醇四硝酸酯[PETNI])介于10到40千克kg之间。峰值恢复研究揭示了峰值程序引入的伪影。如果加标的土壤量(25.0 g)比加标的溶液(1.00 ml)大,则某些土壤的回收率较低。当将2.00 g的土壤样品中掺入1.00 ml的溶液时,回收率接近100%。在埋地雷附近收集的土壤中最常见的分析物是TNT(2-氨基-4,6-二硝基甲苯[2-Am-DNT]和4-氨基-2,6-二硝基甲苯[4-Am- DNT]),制造TNT(2,4-DNT,2,6-DNT。和1,3-DNB)和TNT的杂质。还检测到了DNT和1,3-DNB异构体的微生物还原产物,但ECD对这些化合物的反应较差。

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