紫菜中有机氯农药和多环芳烃的气相色谱-质谱联用测定法  被引量:5

Determination of Organic Chloride Pesticides and Polycyclic Aromatic Hydrocarbons in Prophyra by Gas Chromatograph-Mass Spectrometry

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作  者:王娟[1] 杜鹃[2] 李梦滢[2] 洪颖[2] 程汉宁[2] 倪延延[2] 范春[1] 

机构地区:[1]厦门大学医学院预防医学系,福建厦门361005 [2]厦门大学医学院2005级预防医学专业本科生,福建厦门361005

出  处:《环境与健康杂志》2009年第5期448-450,共3页Journal of Environment and Health

基  金:厦门大学新世纪优秀人才支持计划

摘  要:目的建立测定紫菜中有机氯农药和多环芳烃的气相色谱-质谱分析法。方法紫菜样品经过丙酮-正己烷(体积比为7:3)提取、C18固相萃取柱净化后,采用气相色谱.色谱联用进行定性和定量。结果有机氯农药和多环芳烃的线性范围均为0.01~5.0ug/ml,方法的检出限分别为0.05~0.32ng/g(干重)和0.25~0.56ng/g(干重);有机氯农药的回收率为74.27%-121.49%,平均回收率为91.95%,RSD为3.19%~17.31%;多环芳烃的回收率为65.10%-119.26%,平均回收率为95.60%,RSD为2.75%~14.11%。结论该方法线性关系良好,精密度较高,具有良好的回收率和重复性,可用于紫菜样品中有机氯农药和多环芳烃的检测。Objective To develop an analytical method by gas chromatograph-mass spectrometry (GC-MS) for the determination of organic chloride pesticides and polycyclic aromatic hydrocarbons in prophyra Methods The samples were extracted by an acetone-hexane (7:3, V/V) mixture first, then were purified by C18 solid-phase extraction (SPE), and then were determined with GC-MS. Results The linear range was 0.01-5.0 ug/ml, the limits of detection were 0.05-0.32 ng/g (dry weight) and 0.25-0.56 ng/g (dry weight) for organic chloride pesticides and polycyclic aromatic hydrocarbons respectively. The recovery rates and relative standard deviation for organic chloride pesticides were 74.27%-121.49% and 3.19 %-17.31% relatively; the recovery rates and relative standard deviation for polycyclic aromatic hydrocarbons were 65.10%-119.26% and 2.75%-14.11% relatively. Organic chloride pesticides were partly detected, but the detection rate of polycyelic aromatic hydrocarbons was higher. Fifteen polycychc aromatic hydrocarbons were detected in all samples but dibenz (a,h)-anthracene. Conclusion This method is sensitive, accurate and applicable to the determination of organic chloride pesticides and polycyclic aromatic hydrocarbons in prophyra.

关 键 词:色谱法 气相 农药 紫菜 有机氯农药 多环芳烃 气相色谱-质谱联用 

分 类 号:O657.7[理学—分析化学]

 

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