Laboratório de Sensores Eletroquímicos (LabSensE), Departamento de Química, Universidade Federal do Paraná (UFPR), CEP 81.531-980, Curitiba, PR, Brazil.
Laboratório de Eletroanalítica e Biocombustíveis, Faculdade de Ciências Exatas e Tecnologia, Universidade Federal da Grande Dourados, Rod. Dourados-Itahum, Dourados, MS, Brazil.
Anal Chim Acta. 2017 Aug 29;983:103-111. doi: 10.1016/j.aca.2017.06.025. Epub 2017 Jun 20.
This work reports for the first time the use of chemically activated biochar as electrode modifier for nickel determination. The biochar activation was performed by refluxing with HNO, which promoted a higher nickel preconcentration compared to unmodified and modified biochar precursor electrodes. Morphological and structural characterization revealed the increase of surface acid groups, surface area and porosity of biochar after activation. Nickel determination was investigated adopting an alternative voltammetric methodology based on monitoring the Ni(II)/Ni(III) redox couple. In the proposed method, it was not necessary to use a complexing agent and the biochar itself was responsible for the analyte preconcentration. A linear response for Ni(II) concentration range from 1.0 to 30 μmol L and a limit of detection of 0.25 μmol L were obtained. The method was successfully applied for Ni(II) determination in spiked samples of bioethanol fuel and discharge water, with recoveries values between 103 and 109%.
本工作首次报道了使用化学活化生物炭作为电极修饰剂来测定镍。通过回流 HNO 进行生物炭活化,与未改性和改性生物炭前体电极相比,促进了更高的镍预富集。形貌和结构表征表明,生物炭在活化后表面酸性基团、表面积和孔隙率增加。采用基于监测 Ni(II)/Ni(III) 氧化还原偶的替代伏安测定方法研究了镍的测定。在该方法中,不需要使用络合剂,生物炭本身负责分析物的预富集。获得了 Ni(II)浓度范围为 1.0 至 30 μmol·L 和检测限为 0.25 μmol·L 的线性响应。该方法成功应用于生物乙醇燃料和排放水中加标样品中 Ni(II)的测定,回收率值在 103%至 109%之间。