分析化学
分析化學
분석화학
CHINESE JOURNAL OF ANALYTICAL CHEMISTRY
2009年
12期
1853-1856
,共4页
流动注射%在线萃取%阴离子表面活性剂
流動註射%在線萃取%陰離子錶麵活性劑
류동주사%재선췌취%음리자표면활성제
Flow injection analysis%on-line extraction%anionic surfactants
采用在线微孔膜双萃取-流动注射光度法测定了水中的阴离子表面活性剂.方法基于亚甲基蓝与阴离子表面活性剂作用生成的盐类(λ_(max)=650 nm),可被氯仿萃取,采用在线双微孔膜液液萃取相分离器,优化了流路参数、萃取模块的流路尺寸和微孔膜的孔径.方法的线性范围为25~1000 μg/L,线性相关系数r≥0.999;检出限为4.3 μg/L;不同浓度的相对标准偏差(n=7)为0.7%~6.0%;实际水样的加标回收率为96%~110%;样品测定频率为18样/h.利用本方法分别测定了2个实际水样和2个国家标准参考物质中的阴离子表面活性剂,结果令人满意.
採用在線微孔膜雙萃取-流動註射光度法測定瞭水中的陰離子錶麵活性劑.方法基于亞甲基藍與陰離子錶麵活性劑作用生成的鹽類(λ_(max)=650 nm),可被氯倣萃取,採用在線雙微孔膜液液萃取相分離器,優化瞭流路參數、萃取模塊的流路呎吋和微孔膜的孔徑.方法的線性範圍為25~1000 μg/L,線性相關繫數r≥0.999;檢齣限為4.3 μg/L;不同濃度的相對標準偏差(n=7)為0.7%~6.0%;實際水樣的加標迴收率為96%~110%;樣品測定頻率為18樣/h.利用本方法分彆測定瞭2箇實際水樣和2箇國傢標準參攷物質中的陰離子錶麵活性劑,結果令人滿意.
채용재선미공막쌍췌취-류동주사광도법측정료수중적음리자표면활성제.방법기우아갑기람여음리자표면활성제작용생성적염류(λ_(max)=650 nm),가피록방췌취,채용재선쌍미공막액액췌취상분리기,우화료류로삼수、췌취모괴적류로척촌화미공막적공경.방법적선성범위위25~1000 μg/L,선성상관계수r≥0.999;검출한위4.3 μg/L;불동농도적상대표준편차(n=7)위0.7%~6.0%;실제수양적가표회수솔위96%~110%;양품측정빈솔위18양/h.이용본방법분별측정료2개실제수양화2개국가표준삼고물질중적음리자표면활성제,결과령인만의.
Anionic surfactants in waters were determined using on-line double microporous membrane extraction-flow injection analysis method. This method was based on the extraction of the ion-association complex (λ_(max)=650 nm) which formed from methylene blue cation and anionic surfactants. The on-line double microporous membrane liquid-liquid extraction phase separators were adopted. Optimization of variables of the flow injection manifold, groove mechanical dimension of the phase separator, and pore size of the membrane was performed. The proposed method had a linear range of 25.0-1000.0 μg/L(r≥0.999). The detection limit was 4.28 μg/L. The relative standard deviation(n=7) of different concentration was 0.7%-6.0%. The recovery was between 96%-110% and the sample throughput was 18 h-1. The method was applied to the analysis of standard Reference materials with satisfactory results. For practical application, two water samples were analyzed with the established method.