检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:谭小旺[1] 宋燕西[1] 魏瑞萍[2] 易谷洋[1]
机构地区:[1]东华大学环境科学与工程学院,上海201620 [2]上海新先锋药业有限公司,上海201203
出 处:《分析化学》2012年第9期1409-1414,共6页Chinese Journal of Analytical Chemistry
基 金:中央高校基本科研业务费专项资金(No.2011D11304);科技部公益性行业科研专项(No.GYHY200706036);上海市重点学科建设项目(No.B604)资助
摘 要:建立了三相中空纤维膜液相微萃取-高效液相色谱(HF-LPME-HPLC)方法,用于分析测定水中痕量双酚A的含量。设计了三相中空纤维膜液相微萃取系统,优化的HP-LPME最佳萃取条件为:萃取剂为正辛醇,接受相NaOH浓度为0.09mol/L,样品溶液pH=4.0,NaCl加入量为30g/L,搅拌速度为900r/min,萃取时间为60min。萃取后取20!L接受相进行色谱分析。在最佳萃取条件下,方法的线性范围为0.5~200!g/L(r>0.999),检出限(信噪比为3)为0.2!g/L;富集因子为241;方法RSD<3.2%(n=3)。在实际环境水样中添加5,20和50!g/L的双酚A标准物质,加标平均回收率为92.8%~101.9%。表明本方法可用于水中痕量双酚A的快速准确测定。A method for the determination of trace bisphenol-A (BPA) in water was developed by HPLC using three phase hollow fiber liquid phase microextraction as sample preparation technique. The system of three-phase hollow fiber liquid phase microextraction was designed. The optimized microextraction conditions were as follows: 1-octanol was used as the extraction solvent, the concentration of NaOH solution as acceptor phase was 0.09 mol/L, the pH value of sample solutions was 4.0, the NaC1 concentration in sample solutions was 30 g/L, the stirring rate was 900 r/min and the extraction time was 60 min. The determination of BPA was finished with injecting 20 μL acceptor phase by HPLC. Under the optimal microextraction conditions, the linear range for BPA was 0.5- 200 μg/L (r〉0. 999), the detection limits (S/N=3) of BPA was 0.2 lag/L, the enrichment factor was 241.1, and the relative standard deviations (RSD) was lower than 3.2%. The proposed method was applied to the determination of the BPA in environmental water samples. The spiked average recoveries were within the range of 92.8%-101.9% (n=a). The developed method is simple and environmentally friendly for the determination of BPA in water.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.249