Ravelo-Pérez Lidia M, Hernández-Borges Javier, Angel Rodríguez-Delgado Miguel
Department of Analytical Chemistry, Nutrition and Food Science, University of La Laguna, Tenerife, Canary Islands, Spain.
J Sep Sci. 2008 Oct;31(20):3612-9. doi: 10.1002/jssc.200800352.
In the present work, a GC method with nitrogen-phosphorus detection (NPD) was developed for the simultaneous determination of eight organophosphorus pesticide (OPP) residues (i.e., ethoprofos, diazinon, chlorpyrifos-methyl, fenitrothion, malathion, chlorpyrifos, fenamiphos, and buprofezin) in water samples. Preconcentration of the water samples was carried out using an SPE procedure with multiwalled carbon nanotubes (MWCNTs) of 10-15 nm od, 2-6 nm id, and 0.1-10 microm length as stationary phase. Extraction parameters, such as the amount of MWCNTs, sample volume, pH, and type and amount of the eluent were optimized. The most favorable conditions were as follows: 40 mg MWCNTs, 800 mL water, pH 6.0, and 20 mL dichloromethane, respectively. The MWCNTs-SPE-GC-NPD method was applied to the determination of these pesticides in real water samples: mineral and ground water as well as run-off water from an agricultural area collected shortly before opening out onto the sea. A recovery study was developed with five consecutive extractions of the three types of water spiked at three concentration levels (n = 15). Mean recovery values were in the range of 75-116% for mineral water (RSD < 6.3%), 67-119% for ground water (RSD < 5.8%), and 57-81% for run-off waters (RSDs < 6.9%), except for fenamiphos (mean recovery values between 40 and 84% for the three types of waters, RSDs < 8.9%). LODs were in the low ng/L level (i.e., levels below the maximum residue limits (MRLs) established by the European Union (EU) legislation for these compounds in waters). The proposed method was also applied to the analysis of six water samples (two of each type: mineral, ground, and run-off waters) in which no residues of the selected pesticides were found. Results show that the MWCNTs used in this work have a high adsorbability of the pesticides under study. The main advantage of the use of these MWCNTs is their low cost when compared with those MWCNTs previously used in the literature and with conventional SPE cartridges.
在本研究中,开发了一种采用氮磷检测(NPD)的气相色谱法,用于同时测定水样中的8种有机磷农药(OPP)残留(即乙虫磷、二嗪农、甲基毒死蜱、杀螟硫磷、马拉硫磷、毒死蜱、苯线磷和噻嗪酮)。水样的预浓缩采用固相萃取(SPE)程序,以外径为10 - 15 nm、内径为2 - 6 nm、长度为0.1 - 10微米的多壁碳纳米管(MWCNTs)作为固定相。对MWCNTs的用量、样品体积、pH值以及洗脱剂的类型和用量等萃取参数进行了优化。最适宜的条件如下:MWCNTs用量为40 mg、水样体积为800 mL、pH值为6.0、二氯甲烷用量为20 mL。MWCNTs - SPE - GC - NPD方法应用于实际水样中这些农药的测定:矿泉水、地下水以及在流入大海前不久采集的农业区域的径流水中的农药残留。对三种类型的水在三个浓度水平下进行加标,连续萃取5次开展回收率研究(n = 15)。矿泉水的平均回收率在75 - 116%之间(相对标准偏差< 6.3%),地下水的平均回收率在67 - 119%之间(相对标准偏差< 5.8%),径流水中的平均回收率在57 - 81%之间(相对标准偏差< 6.9%),苯线磷除外(三种类型水的平均回收率在40 - 84%之间,相对标准偏差< 8.9%)。检测限处于低纳克/升水平(即低于欧盟法规对水中这些化合物规定的最大残留限量(MRL))。该方法还应用于分析6个水样(每种类型各2个:矿泉水、地下水和径流水中的农药残留),未检测到所选农药的残留。结果表明,本研究中使用的MWCNTs对所研究的农药具有高吸附性。与文献中先前使用的MWCNTs以及传统的SPE小柱相比,使用这些MWCNTs的主要优点是成本低。