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作 者:周围[1,2] 解迎双[2] 王波[1] 贾松涛[3] 牛洪亮[3]
机构地区:[1]甘肃出入境检验检疫局中心实验室,甘肃兰州730020 [2]西北师范大学地理与环境科学学院,甘肃兰州730070 [3]甘肃农业大学食品科学与工程学院,甘肃兰州730070
出 处:《分析测试学报》2011年第1期95-98,共4页Journal of Instrumental Analysis
摘 要:建立了水中4种直链烷基苯磺酸钠的固相萃取/高效液相色谱的测定方法。样品经高速冷冻离心,用MAX复合阴离子交换小柱净化富集后直接进样。在以乙腈-100mmol/L乙酸铵(体积比73:27)为流动相,流速1mL/min,柱温30℃,检测波长225nm,进样体积10灿的条件下,4种直链烷基苯磺酸钠得到很好的分离。在优化实验条件下,十一烷基苯磺酸钠与十三烷基苯磺酸钠的线性范围为10~50mg/L,检出限为10mg/L,十二烷基苯磺酸钠与十四烷基苯磺酸钠的线性范围为5~25mg/L,检出限为5mg/L;加标回收率为86%~98%;相对标准偏差为2.9%~7.4%。A solid phase extraction coupled with high performance liquid chromatographic (SPE/ HPLC) method was established for the determination of 4 kinds of sodium n-alkyl benzene sulfonates in water. The samples were refrigerated and centrifuged, then purified and enriched with MAX com- plex anion exchange column. Four sodium n-alkyl benzene sulfonates were successfully separated by HPLC using acetonitrile- 100 mmoL/L ammonium acetate (73 : 27, by volume) as mobile phase with a flow rate of 1 mL/min, column temperature of 30℃, detection wavelength of 225 nm and injection volume of 10 μL. Under the optimal conditions, the calibration curves were linear in the range of 10 -50 mg/L for sodium undecylbenzene snlfonte and sodium N-tridecylbenzene sulfonate with detection limits of 10mag/L, and 5 - 25 mg/L for sodium dodecylbenzene sulphonate and sodium tetradecylbenzene sulfonate with detection limits of 5 mg/L. The spiked recoveries were in the range of 86% - 98% with relative standard deviations(RSDs) of 2.9% - 7.4% .
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