期刊文献+

高效液相色谱法同时测定玉米及土壤中莠去津和绿麦隆的残留量 被引量:2

Determination of atrazine and chlorotoluron residue in corn and soil by high performance liquid chromatography
原文传递
导出
摘要 目的:建立玉米及土壤中残留的莠去津和绿麦隆高效液相色谱法同时测定方法。方法:样品经提取后,利用硅胶柱固相萃取净化技术,采用C18柱分离,甲醇-水梯度洗脱,检测波长216 nm。结果:在2种基质中,莠去津和绿麦隆能得到良好分离,莠去津在3.2-200 ng呈线性,r=0.9999,绿麦隆在6.5-80 ng呈线性,r=0.9999,回收率为93.3%-103.3%,RSD为1.72%-3.76%(n=6),方法检出限为莠去津0.03 mg/kg,绿麦隆0.02 mg/kg。结论:利用本方法,2种除草剂能得到良好的分离,经净化后利用梯度洗脱,可消除杂峰的干扰,分离完全且峰形较好,回收率高,易于操作,是测定玉米及土壤中2种除草剂的有效定量方法。 Objective:To develop a high performance liquid chromatography method for determination of atrazine and chlorotoluron residue in corn and soil. Methods : After extraction, the sample extracant was cleaned - up with silica gel solid phase column, and finally it was separated using Cls column by use of gradient elution with methanol - water and detected at 216nm. Results:In both matrixes, atrazine and chlorotoluron could be well separated. The linearity range for atrazine and chlorotoluron was 3.2 ~ 200 ng and 6. 5 - 80 ng, respectively. The correlation coefficients for atrazine and chlorotoluron were both greater than 0. 9999. The recoveries were between 93.3% - 103.3% , with RSD between 1.72% - 3.76%. The method detection limits for atrazine and ehlorotoluron were 0.03 mg/kg and 0.02 mg/kg. Conclusion: This method is simple with high recoveries. It is suitable for measurement of atrazine and chlorotoluron.
出处 《中国卫生检验杂志》 CAS 2009年第10期2272-2273,2288,共3页 Chinese Journal of Health Laboratory Technology
关键词 高效液相色谱法 莠去津 绿麦隆 玉米及土壤 硅胶柱 固相萃取 净化 梯度洗脱 HPLC atrazine Chlorotoluron Corn Soil HPLC
作者简介 汤鋆(1977-),男,主管技师,主要从事理化检验工作。
  • 相关文献

参考文献4

二级参考文献6

共引文献15

同被引文献14

  • 1王以燕,孙绮丽,张百臻.反相高效液相色谱法测定绿麦隆[J].色谱,1994,12(4):291-292. 被引量:1
  • 2徐远金,李永库.蔬菜中阔草清等8种农药残留量的高效液相色谱-质谱分析[J].分析试验室,2006,25(11):74-78. 被引量:6
  • 3宋宁慧,朱红梅,杨红.差示扫描量热法测定除草剂绿麦隆的纯度[J].分析科学学报,2007,23(1):54-56. 被引量:5
  • 4GB/T5009.132-2003.食品中莠去津残留量的测定[s].
  • 5聂果,吴春先,高立明,王广成,陈丙坤,张中明.莠去津的生态毒理学及其环境行为学研究进展[J].现代农药,2007,6(4):32-37. 被引量:17
  • 6SN/T1972-2007.进出口食品中莠去津残留量的检测方法气相色谱-质谱法[S].
  • 7RICHTER W. Primary Methods of Measurement in Chemical Analysis[J]. Accreditation and Quality Assurance, 1997, 2(8): 353- 354.
  • 8LIU S Y, HU C Q. A Comparative Uncertainty Study of the Calibration of Macrolide Antibiotic Reference Standards Using Quantitative Nuclear Magnetic Resonance and Mass Balance Methods[J]. Analytica Chimica Acta, 2007, 602(1): 114-121.
  • 9WHO Expert Committee on Specifications for Pharmaccutial Preparations. General Guidelines for the Establishment, Maintenance and Distribution of Chemical Reference Substance[S]. Geneva, World Health Organization, 1999(WHO Technical Reports Series, No.885, Annex 3).
  • 10WHO Expert Committee on Specifications for Pharmaccutial Preparations. Evaluation of Chemical Reference Substance, in International Pharmacopoeia[S]. Geneva, World Health Organization, 2003.

引证文献2

二级引证文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部