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在导电金刚石电极上对氨基甲酸酯类农药进行电化学检测。

Electrochemical detection of carbamate pesticides at conductive diamond electrodes.

作者信息

Rao Tata N, Loo B H, Sarada B V, Terashima C, Fujishima A

机构信息

Department of Applied Chemistry, School of Engineering, The University of Tokyo, Japan.

出版信息

Anal Chem. 2002 Apr 1;74(7):1578-83. doi: 10.1021/ac010935d.

Abstract

Conductive boron-doped diamond thin-film electrodes were used for the electrochemical detection of selected N-methylcarbamate pesticides (carbaryl, carbofuran, methyl 2-benzimidazolecarbamate, bendiocarb) after liquid chromatographic separation. Two kinds of detection methods were adopted in this study. In the first method, a direct detection of underivatized pesticides was carried out at an operating potential of 1.45 V versus Ag/AgCl, which resulted in the detection limits of 5-20 ng/mL (or 5-20 ppb) with S/N = 2 due to the low background current and wide potential window of the diamond electrode. In the second method, the detection limits were improved by subjecting the pesticide samples to alkaline hydrolysis in a separate step prior to injection. The phenolic derivatives obtained by alkaline hydrolysis oxidize at a relatively lower potential (0.9 V vs Ag/AgCl), which increases the sensitivity drastically. The advantage of the diamond electrode for the detection of phenolic derivatives is that it offers excellent stability in comparison to other electrodes. This method gives the detection limits of 0.6-1 ng/mL (or 0.6-1 ppb), which are well below the maximum residue levels allowed for carbaryl, carbofuran, and bendiocarb. While the lowest detection limits (LOD) obtained by the direct detection of pesticides are comparable to the those reported by the well-established HPLC-fluorescence, the LODs of the alkaline hydrolysis method are found to be even lower than the reported limits. On-line reactivation of the diamond electrode surface was shown to be possible by an anodic treatment of the electrode at approximately 3 V for 30 min in case of electrode fouling, which may occur after a prolonged use. Such a treatment damages the glassy carbon (GC) and metal electrodes, while the diamond electrode remains stable. These results suggest that the diamond electrode is superior to the other previously used electrodes such as GC and Kelgraf type for highly sensitive and stable detection of carbamate pesticides.

摘要

导电硼掺杂金刚石薄膜电极用于在液相色谱分离后对选定的氨基甲酸酯类农药(西维因、克百威、多菌灵、仲丁威)进行电化学检测。本研究采用了两种检测方法。在第一种方法中,在相对于Ag/AgCl为1.45 V的工作电位下对未衍生化的农药进行直接检测,由于金刚石电极的背景电流低且电位窗口宽,检测限为5 - 20 ng/mL(或5 - 20 ppb),信噪比(S/N)= 2。在第二种方法中,通过在进样前单独对农药样品进行碱性水解来提高检测限。碱性水解得到的酚类衍生物在相对较低的电位(相对于Ag/AgCl为0.9 V)下氧化,这极大地提高了灵敏度。金刚石电极用于检测酚类衍生物的优点是与其他电极相比具有出色的稳定性。该方法的检测限为0.6 - 1 ng/mL(或0.6 - 1 ppb),远低于西维因、克百威和仲丁威允许的最大残留量。虽然通过直接检测农药获得的最低检测限(LOD)与成熟的HPLC - 荧光法报道的相当,但碱性水解法的LOD甚至低于报道的限值。在电极污染(长时间使用后可能发生)的情况下,通过在约3 V下对电极进行30分钟的阳极处理,可实现金刚石电极表面的在线再活化。这种处理会损坏玻璃碳(GC)和金属电极,而金刚石电极保持稳定。这些结果表明,在对氨基甲酸酯类农药进行高灵敏度和稳定检测方面,金刚石电极优于其他先前使用的电极,如GC电极和Kelgraf型电极。

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