Pon Saravanan N, Venugopalan S, Senthilkumar N, Santhosh P, Kavita B, Gurumallesh Prabu H
High Energy Materials Research Laboratory, Pune 411021, India.
Talanta. 2006 May 15;69(3):656-62. doi: 10.1016/j.talanta.2005.10.041. Epub 2005 Dec 20.
The contamination of soil by nitroaromatic and nitramine explosives is widespread during the manufacture, testing and disposal of explosives and ammunitions. The analysis for the presence of trace explosive contaminants in soil becomes important in the light of their effect on the growth of different varieties of plants and crops. 2,4,6-Trinitrotoluene (TNT), cyclotrimethylene trinitramine (Research Department explosive, RDX) and cyclotetramethylene tetranitramine (high melting point explosive, HMX), other related explosive compounds and their by-products must be monitored in soil and surrounding waterways since these are mutagenic, toxic and persistent pollutants that can leach from the contaminated soil to accumulate in the food chain. In this study, a voltammetric method has been developed for the determination of explosive such as RDX, HMX and TNT. The electrochemical redox behavior of RDX, HMX and TNT was studied through cyclic voltammetry and quantitative determination was carried out by using square wave voltammetry technique. Calibration curves were drawn and were linear in the range of 63-129ppm for RDX with a detection limit of 10ppm, 49-182ppm for HMX with a detection limit of 1ppm and 38-139ppm for TNT with a detection limit of 1ppm. This method was applied to determine the contaminations in several soil samples that yielded a relative error of 1% in the concentrations.
在炸药和弹药的制造、测试及处置过程中,土壤受到硝基芳香族和硝胺类炸药的污染十分普遍。鉴于微量炸药污染物对不同种类植物和作物生长的影响,分析土壤中痕量炸药污染物的存在情况变得至关重要。必须对土壤及周边水道中的2,4,6-三硝基甲苯(TNT)、环三亚甲基三硝胺(研究部炸药,RDX)和环四亚甲基四硝胺(高熔点炸药,HMX)、其他相关炸药化合物及其副产物进行监测,因为这些都是具有致突变性、毒性且持久的污染物,会从受污染土壤中渗出并在食物链中累积。在本研究中,已开发出一种伏安法用于测定RDX、HMX和TNT等炸药。通过循环伏安法研究了RDX、HMX和TNT的电化学氧化还原行为,并采用方波伏安法技术进行定量测定。绘制了校准曲线,RDX在63 - 129ppm范围内呈线性,检测限为10ppm;HMX在49 - 182ppm范围内呈线性,检测限为1ppm;TNT在38 - 139ppm范围内呈线性,检测限为1ppm。该方法用于测定多个土壤样品中的污染物,浓度相对误差为1%。