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作 者:李先国[1] 阎国芳 周晓[1,3] 虢新运[1] 王岩[1] 刘金燕[1]
机构地区:[1]中国海洋大学海洋化学理论与工程技术教育部重点实验室,山东青岛266100 [2]青岛市产品质量监督检验所,山东青岛266061 [3]国家质量监督检验检疫总局,北京100088
出 处:《中国海洋大学学报(自然科学版)》2009年第5期1087-1092,共6页Periodical of Ocean University of China
基 金:国家自然科学基金项目(20775074)资助
摘 要:建立了用固相萃取-高效液相色谱-荧光检测法测定海水中多环芳烃的方法,优化了色谱条件和萃取条件。除苊不能用荧光检测器检出外,其余15种多环芳烃的空白加标回收率在64.5%(苯并[g,h,i],茚并[1,2,3-cd]芘)~88.7%(苯并[a]蒽)之间,相对标准偏差(n=5)为4.9%(荧蒽,苯并[b]荧蒽)~11.1%(苯并[g,h,i],茚并[1,2,3-cd]芘),方法的检出限在0.72(蒽)~14.10 ng/L(荧蒽)之间,基本上达到了痕量分析的要求。利用该方法测得青岛湾表层海水中多环芳烃的浓度在0.125(苯并[k]荧蒽)~25.996 ng/L(萘)之间,但苯并[a]芘未检出。A method using solid phase extraction-high performance liquid chromatography with fluorescent detection was established for the determination of polycyclic aromatic hydrocarbons in seawater; the chromatographic and extraction conditions were optimized. With exception of acenaphthylene which was not fluorescently detected, the recoveries of other 15 PAHs were between 64.5 % (for benzo [g, h, i] perylene and indeno [ 1,2, 3-cd] pyrene) and 88.7 % (for benzo[ a] anthracene), the relative standard deviations( n = 5) ranged from 4.9% (for fluoranthene and benzo [b] fluoranthene) to 11.1% (for benzo [g, h, i] perylene and indeno [1,2, 3-cd] pyrene), and the method detection limits were 0.72 ng/L(for anthracene.) to 14.10 ng/L(for fluoranthene). The concentrations of polycyclic aromatic hydrocarbons in surface seawater of Qingdao bay area determined by this method ranged from 0. 125 ng/L(for benzo [ k] fluorathene) to 25. 996 ng/L(for naphthalene) while benzo [a] pyrene was not detected.
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