首页 | 本学科首页   官方微博 | 高级检索  
     检索      

土壤总砷测定前处理方法探讨
引用本文:邹强,刘芳,龚世龙,杨剑虹.土壤总砷测定前处理方法探讨[J].土壤通报,2011(6):1341-1344.
作者姓名:邹强  刘芳  龚世龙  杨剑虹
作者单位:涪陵区农业委员会;西南大学资源环境学院;
基金项目:国家科技支撑项目(2007BAD87B10)资助
摘    要:采用加标回收方法比较研究了5种土壤总砷测定的前处理方法(分别为浓HNO3-浓H2SO4-HC1O4法、王水法、浓HNO3-浓H2SO4-V2O5法、浓HNO3-浓H2SO4-V2O5Ⅰ法和浓HNO3-浓H2SO4-V2O5Ⅱ法),结果表明,5种前处理方法的加标回收率在89.9%~102%之间,变异系数在0.56%~5.27%之间。其中,浓HNO3-浓H2SO4-V2O5Ⅰ法处理,土壤所用消解时间40min左右,其回收率较高,在98.5%~99.1%之间,变异系数较小,在0.56%~0.85%之间;该前处理方法具有消解时间最短、加标回收率和精密度高及重现性最好的特点,优于其他4种前处理方法,可作为推荐方法应用。

关 键 词:土壤  总砷测定  前处理  加标回收

Study on the Pretreatment for Determination of Soil Total Arsenic
ZOU Qiang ,LIU Fang ,GONG Shi-long ,YANG Jian-hong.Study on the Pretreatment for Determination of Soil Total Arsenic[J].Chinese Journal of Soil Science,2011(6):1341-1344.
Authors:ZOU Qiang    LIU Fang  GONG Shi-long  YANG Jian-hong
Institution:ZOU Qiang 1,2,LIU Fang 1,GONG Shi-long 1,YANG Jian-hong 2(1.Fuling agriculture commission,Fuling 408000,China,2.College of Resources and Enviroment,Southwestern University,Chongqing 400715,China)
Abstract:A recovery experiment by adding standard arsenic to soil was conducted to compare the five kinds of pretreatment methods for determination of soil total arsenic(HNO3-H2SO4-HC1O4 method,aqua regia method,HNO3-H2SO4-V2O5 method,HNO3-H2SO4-V2O5Ⅰmethod and HNO3-H2SO4-V2O5Ⅱmethod).Results showed that the recovery of standard addition of the 5 methods varied in the range of 89.9% to 102%,while their coefficients of variation were 0.56% to 5.27%.Among these pretreatment methods,the HNO3-H2SO4-V2O5Ⅰmethod had a higher recovery of standard addition(98.5%-99.1%) and lower coefficient of variation(0.56% ~ 0.85%),while its digestion time was about 40 minuets.Compared to the other 4 pretreatment methods,the HNO3-H2SO4-V2O5Ⅰmethod had the shortest digestion time,highest recovery of standard addition,highest precision and best reproducibility,therefore could be applied as the recommended method.
Keywords:Soil  Determination of total arsenic  Pretreatment  Recovery of standard  
本文献已被 CNKI 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号