首页> 外文期刊>Analytical chemistry >Electrochemical oxidation of chlorophenols at a boron-doped diamond electrode and their determination by high-performance liquid chromatography with amperometric detection
【24h】

Electrochemical oxidation of chlorophenols at a boron-doped diamond electrode and their determination by high-performance liquid chromatography with amperometric detection

机译:掺硼金刚石电极上氯酚的电化学氧化及高效液相色谱-安培检测法测定

获取原文
获取原文并翻译 | 示例
       

摘要

Anodically pretreated. diamond electrodes have been used for the detection of chlorophenols (CPs) in environmental water samples after high-performance liquid chromatographic (HPLC separation. The anodization of as-deposited boron-doped polycrystalline diamond thin-film electrodes has enabled the stable determination of phenols over a wide concentration range. Prior to the HPLC analysis, a comparative study with ordinary glassy carbon, as-deposited diamond, and anodized diamond was made to examine the oxidative behavior of phenols by cyclic voltammety and flow injection analysis with amperometric detection. At anodized diamond electrodes, reproducible, well-defined cyclic voltammograms were obtained even at high CP concentration (5 mM), due to a low proclivity for adsorption of the oxidation products on the surface. In addition, after prolonged use, the partially deactivated diamond could be reactivated on line by applying a highly anodic potential (2.64 Vvs SCE) for 4 min, which enabled the destruction of the electrodeposited polymer deposits. Hydroxyl radicals produced by the high applied potential, in which oxygen evolution occurs, are believed to be responsible for the oxidation of the passivating layer on the surface. When coupled with flow injection analysis (FIA), anodized diamond exhibited excellent stability, with a response variability of 2.3% (n = 100), for the oxidation of a high concentration (5 mM) of chlorophenol. In contrast, glassy carbon exhibited a response variability of 39.1%. After 100 injections, the relative peak intensity, for diamond decreased by 10%, while a drastic decrease of 70% was observed for glassy carbon. The detection limit obtained in the FIA mode for 2,4-dichlorophenol was found to be 20 nM (S/N = 3), with a linear dynamic range up to 100 muM. By coupling with the column-switching technique, which enabled on-line preconcentration (50 times), the, detection limit was lowered to 0.4 nM (S/N = 3). By use of this technique, anodized diamond electrodes were demonstrated for the analysis of CPs in drainwater that was condensed from the flue gas of waste incinerators. [References: 44]
机译:阳极预处理。高效液相色谱(HPLC分离)后,金刚石电极已用于检测环境水样中的氯酚(CPs)。沉积的硼掺杂多晶金刚石薄膜电极的阳极氧化使得能够稳定地测定苯酚在进行HPLC分析之前,进行了与普通玻璃碳,沉积金刚石和阳极氧化金刚石的对比研究,通过循环伏安法和安培检测法进行流动注射分析,研究了酚的氧化行为。电极,即使在高CP浓度(5 mM)时,由于在表面上吸附氧化产物的可能性较低,也可以获得可再现的,清晰的循环伏安图,此外,长时间使用后,部分失活的金刚石可以重新活化通过施加高阳极电位(2.64 Vvs SCE)持续4分钟在线,从而可以破坏t他电沉积了聚合物沉积物。据信由高施加电势产生的羟基自由基(其中会发生氧气逸出)是造成表面钝化层氧化的原因。与流动注射分析(FIA)结合使用时,阳极氧化的钻石表现出出色的稳定性,对于高浓度(5 mM)的氯酚氧化反应响应性为2.3%(n = 100)。相比之下,玻璃碳表现出39.1%的响应变异性。注射100次后,金刚石的相对峰强度降低了10%,而玻璃碳则急剧降低了70%。发现在FIA模式下获得的2,4-二氯苯酚的检出限为20 nM(S / N = 3),线性动态范围高达100μM。通过与可进行在线预浓缩(50次)的列切换技术相结合,检测限降低到0.4 nM(S / N = 3)。通过使用该技术,演示了阳极氧化金刚石电极,用于分析废水焚烧炉烟气中冷凝的废水中的CP。 [参考:44]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号