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:宋娟 李晓燕[2] 张升晓[2] 张媛媛[2] 刘军深[2] 徐强[2]
机构地区:[1]烟台市环境监察大队,烟台264003 [2]鲁东大学化学与材料科学学院,烟台264025
出 处:《分析试验室》2014年第12期1374-1377,共4页Chinese Journal of Analysis Laboratory
基 金:国家自然科学基金(21207059;21171085);山东省自然科学基金(ZR2011BQ012)项目资助
摘 要:制备了一种新型的磁性纳米吸附剂—巯基修饰的Fe3O4@SiO2,并将其用作固相萃取剂从环境水样中富集痕量Hg^2+,采用原子荧光分光光度计测定富集后的Hg^2+。研究了吸附剂用量、pH、平衡时间、洗脱条件及吸附剂重复使用次数对Hg^2+回收率的影响。利用该磁性固相萃取方法建立了标准曲线,并用于测定实际水样中的Hg^2+含量。方法的检测限为0.1 ng/L,加标回收率为95%-104%,相对标准偏差0.1%-0.6%。Mercury exists in environmental water at trace level. To monitor trace mercury pollution in environment water,preconcentration and purification are necessary before instrument measurement. There are some disadvantages in traditional methods,such as low efficiency,fussy operation,time-consuming. In this study a novel Fe3O4@ Si O2-SH sorbent was synthesized and used as a solid phase extraction( SPE) sorbent to extract trace Hg2 +from environmental water samples,and then the concentration of Hg2 +was determined with a hydride generation-atomic fluorescence spectrophotometer. Effects of amount of sorbent, solution p H,equilibrium time,desorption condition,and recycle time on recovery of Hg2 +were studied in detail. The standard curve was obtained based on the magnetic SPE method,and the proposed method was successfully applied to the determination of trace Hg2 +in some environmental water. The detection limit was 0. 1 ng / L,and the recoveries rates of the spiked water samples ranged from 95% to 104% with relative standard deviations( RSD) varying from 0. 1% to 0. 6%,exhibiting high sensitivity,wide linear range and good precision. This study not only developed a simple, convenient, and high sensitive method to determine trace Hg2 +in environmental water,but also opened up a new avenue for application of magnetic SPE.
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:216.73.216.15