首页> 外文学位 >Development of an analytical method for the determination of extractable nitroaromatics and nitramines in soils.
【24h】

Development of an analytical method for the determination of extractable nitroaromatics and nitramines in soils.

机译:建立一种测定土壤中可萃取硝基芳香烃和硝胺的分析方法。

获取原文
获取原文并翻译 | 示例

摘要

n analytical method was developed to determine the concentrations of HMX, RDX, TNB, DNB, tetryl, TNT and 2,4-DNT in soil. The method relies on solvent extraction with analysis by reversed-phase liquid chromatography.;The extraction step was studied in terms of process kinetics and recovery. Two solvents (acetonitrile and methanol) and four extraction techniques (Soxhlet, ultrasonic bath, mechanical shaker and homogenizer-sonicator) were compared. Ultrasonic bath extraction with acetonitrile was selected based on extraction kinetics, overall analyte recovery, sample throughput, and instability of analytes at elevated temperature. The rate of extraction of analytes from field-contaminated soil was shown to be much slower than from spiked soils, indicating it is unwise to develop extraction procedures based solely on spiked materials.;A number of possible separations were examined. Adequate separation of the seven analytes was achieved on an LC-18 column eluted with 1:1 methanol/water with a run time under 15 minutes. Confirmation of analyte identities was recommended on LC-CN, also eluted with 1:1 methanol/water. Elution orders on the two columns were quite different due to different mechanisms of separation.;Additional tests were conducted to assess various sample processing alternatives. Removal of particulates from soil extracts was achieved by dilution of extracts 1:1 with aqueous CaCl;The overall method provides linear calibration curves over a wide range of analyte concentrations. Detection limits ranged from 0.03 to 1.27
机译:开发了一种分析方法来测定土壤中HMX,RDX,TNB,DNB,tetryl,TNT和2,4-DNT的浓度。该方法依赖于溶剂萃取,并通过反相液相色谱法进行分析。;从工艺动力学和回收率的角度研究了萃取步骤。比较了两种溶剂(乙腈和甲醇)和四种萃取技术(索氏萃取,超声浴,机械振荡器和均质超声仪)。根据萃取动力学,整体分析物回收率,样品通量和高温下分析物的不稳定性,选择使用乙腈进行超声浴萃取。结果表明,从田地污染土壤中提取分析物的速度要比加标土壤慢得多,这表明仅基于加标物质开发提取方法是不明智的。研究了许多可能的分离方法。在LC-18色谱柱上用1:1甲醇/水洗脱,可在7分钟内充分分离7种分析物,运行时间不超过15分钟。建议在LC-CN上确认分析物的身份,并用1:1甲醇/水洗脱。由于分离机理不同,两根色谱柱的洗脱顺序有很大不同。;进行了其他测试,以评估各种样品处理方法。通过用氯化钙水溶液将提取物1:1稀释来去除土壤提取物中的颗粒物;整体方法可在较宽的分析物浓度范围内提供线性校准曲线。检测限范围为0.03至1.27

著录项

  • 作者

    Jenkins, Thomas F.;

  • 作者单位

    University of New Hampshire.;

  • 授予单位 University of New Hampshire.;
  • 学科 Analytical chemistry.
  • 学位 Ph.D.
  • 年度 1989
  • 页码 186 p.
  • 总页数 186
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号