摘要
采用GC-μECD建立了一种持久性有机污染物五氯酚在土壤、水及植株中的残留检测方法,并对残留分析的各种条件进行了优化.用石油醚和稀硫酸振荡提取90rain,碳酸钠反萃取后,在pH为9的条件下采用衍生萃取同步处理样品20min,以GC-μECD分离测定.实验结果表明在10-1000μg/L范围内,五氯酚浓度与色谱峰面积有很好的线性关系,其回归方程为Y=-62.71+11.61X,相关系数为0.9993,检出限为6.18μg/L.该方法的加标回收率为81.7%~99.4%,相对标准偏差1.05%-4.53%,方法简便、快速、灵敏、准确.
A method for determining residues (POPS) pentachlorophenol(PCP) in environment of the persistent organic pollutants was founded by means of GC-μECD. Samples were extracted with petroleum ether and dilute sulphuric acid about 90 minutes by means of vibrating, and re-extracted with sodium carbonate, derivated with acetic anhydride about 20 minutes under the condition of pH 9 and at the same time extracted, finally analyzed by GC-μECD. The recovery rates ranged from 81.7% to 99.4% and RSD varied between 1, 05% and 4.53%. Generally speaking, the method was simple, sensitive, stable, quick and can be used as a routine method for determination of trace PCP in environment.
出处
《华中师范大学学报(自然科学版)》
CAS
CSCD
2006年第4期540-543,547,共5页
Journal of Central China Normal University:Natural Sciences
基金
教育部科学技术研究重点项目(教技司[2005]41号)
留学回国基金项目(教外司留[2004]527号)