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A oxidação eletrocatalítica de hidrazina foi estudada sobre um eletrodo de grafite pirolítico ordinário modificado com tetrapiridinoporfirazina de ferro (FeTPyPz) com as técnicas de voltametria cíclica e de eletrodo de disco rotatório. Análise dos voltamogramas registrados a diferentes velocidades de varredura do potencial e das curvas de polarização para diferentes velocidades de rotação do eletrodo mostraram que a reação de eletroxidação de hidrazina sobre FeTPyPz processa-se de acordo com um mecanismo envolvendo 4 elétrons e com a formação de N 2 como principal produto. Os parâmetros cinéticos sugerem que a segunda etapa de transferência de carga é a etapa determinante da velocidade da reação. A atividade eletrocatalítica do complexo FeTPyPz depende do potencial formal do processo redox Fe(II)/Fe(I), que apresentou bom ajuste num gráfico do tipo vulcano formado por diferentes ftalocianinas de ferro, indicando que este potencial formal é um bom indicador da reatividade destes complexos.The electrocatalytic oxidation of hydrazine was studied using an ordinary pyrolytic graphite electrode modified with iron tetrapyridinoporphyrazine complex (FeTPyPz), employing cyclic voltammetry and rotating disk electrode techniques. Analyses of the voltammograms recorded at different potential scan rates and the polarization curves at different electrode rotation rates showed that the reaction of electrooxidation of hydrazine on FeTPyPz occurs via 4-electrons with the formation of N 2 as main product. The kinetic parameters suggest that the second electron transfer step is rate controlling. The activity of FeTPyPz depends on its Fe(II)/Fe(I) formal potential and fits well in a volcano plot that includes several iron phthalocyanines, indicating that such formal potential is a good reactivity index for these complexes.Keywords: hydrazine oxidation, modified graphite electrode, iron tetrapyridinoporphyrazine, volcano plot IntroductionThe study of chemically modified electrodes has attracted considerable interest in the last decades as researchers attempt to exert more control over the chemical nature of the electrode surface. Molecules of known reactivity are then incorporated or confined on the electrode surface, acting as mediators for electron transfer reactions. Applications include electrocatalysis, electroanalysis, sensors and biosensors, as well as in electrochemical detection systems used in flow-injection analysis or high performance liquid chromatography. One applicability of these electrodes refers to the oxidation and detection of hydrazine, an important chemical compound used in jet and rocket fuels and in the production of agricultural and textile chemicals, drugs, explosives, photographic developers, blowing agents used in the manufacture of foam rubber, and in the prevention of rusting in boilers and nuclear reactors. 31 Furthermore, the detection of hydrazine and its derivatives is very important in pharmacology due to the recognition as carcinogenic and hepatotoxic substances. 31,32 In order to reduce the typi...

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O presente trabalho descreve uma metodologia analítica para determinação simultânea de ácido ascórbico (AA) e ácido úrico (AU) por voltametria de pulso diferencial empregando o surfactante catiônico cloreto de cetilpiridínio. Medidas voltamétricas de pulso diferencial realizadas em pH 7,0 revelaram que o meio micelar catiônico permite separar em 282 mV os picos de oxidação de AA e AU na mesma solução, valor suficiente para determinar ambas as espécies simultaneamente. Como em pH 7,0 o AA está mais ionizado que o AU, sua atração eletrostática em direção às micelas catiônicas, formadas sobre a superfície do eletrodo de carbono vítreo, é maior; desta forma, promove a diminuição no sobrepotencial e o aumento na taxa de transferência de elétrons. Foram construídas curvas de calibração para AA e AU na faixa de concentração de 4,70 até 220 µmol L -1 e 0,50 até 110 µmol L -1 . A metodologia proposta foi aplicada para a determinação de AA e AU em amostras de urina humana.The present work describes an analytical methodology for simultaneous determination of ascorbic acid (AA) and uric acid (UA) by differential pulse voltammetry employing the cationic surfactant, cetylpyridinium chloride. Differential pulse voltammetry measurements revealed that the cationic micellar media may separate the oxidation peak potentials of AA and UA present in the same solution by about 282 mV, which is enough to determine both species simultaneously. As in pH 7.0 the AA is more ionized than UA, its electrostatic attraction towards the cationic micelles formed onto the surface of glassy carbon electrode is higher, therefore, promoting a decrease in the overpotential and increasing the electron transfer rate. Calibration curves to AA and UA in the concentration range from 4.70 up to 220 µmol L -1 and 0.50 up to 110 µmol L -1 were built. The proposed methodology was applied for the simultaneous determination of AA and UA in human urine samples.Keywords: uric acid, ascorbic acid, differential pulse voltammetry, cationic surfactant, micelles IntroductionAscorbic acid (AA) and uric acid (UA) coexist in biological fluids such as blood and urine, 1 being in practical medicine, necessary to determine AA and UA simultaneously. Ascorbic acid (a water soluble vitamin C) plays a vital role in processes of oxidation and reduction in the human organism by participating in many metabolic reactions. 2 AA has also been used to prevent and treat the common cold, mental illness, infertility and cancer. 3 Moreover, ascorbic acid has also been used clinically in the treatment and prevention of scurvy. 4 Uric acid (2,6,8-trihydroxypurine, UA) is the primary product of purine metabolism in the human body and is formed in liver and tissues during the oxidation of aminopurines. 5 Its abnormal concentration level in urine and serum are symptoms of several diseases like gout, hyperuricaemia and Lesch-Nyhan syndrome. 6,7 For instance, the concentration of uric acid in the blood of patients suffering from gout increases up to 1 mmol L -1 , which is above the concentration ...

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ABSTRACT. Ascorbic acid (AA) is an important compound of the human diet, in the metabolism acting mainly as exogenous antioxidant. A method for electrochemical detection of Ascorbic acid (AA) with a GCE was developed using a cationic surfactant cetylpyridinium chloride (CPC). The presence of CPC influences the electrochemical behaviour of AA, reduces the applied potential to measure AA oxidation followed by an increase in the peak current. In the optimized conditions the AA determination was possible in the linear range of 5.0 x 10 . The applicability of the method is in the sensitivity and selectivity of the GCE for the AA detection as well as the simplicity of the demonstrated method using an electrode without modifying and without pre-treatment of samples. Recovery tests presented values of 98 -103% suggesting the method has no significant interference and making possible to be successfully used for AA determination in complex samples.