Probing the Use of Homemade Carbon Fiber Microsensor for Quantifying Caffeine in Soft Beverages

Author:

de Freitas Araújo Karla Caroline1,de Araújo Costa Emily Cintia Tossi1,de Araújo Danyelle Medeiros12ORCID,Santos Elisama V.23ORCID,Martínez-Huitle Carlos A.12ORCID,Castro Pollyana Souza1

Affiliation:

1. Institute of Chemistry, Federal University of Rio Grande do Norte, Av. Campus Universitário, Av. Salgado Filho 3000, Lagoa Nova, Natal CEP59078-970, RN, Brazil

2. National Institute for Alternative Technologies of Detection, Toxicological Evaluation and Removal of Micropollutants and Radioactives (INCT-DATREM), Institute of Chemistry, Universidade Estadual Paulista, Araraquara CEP14800-900, SP, Brazil

3. School of Science and Technology, Federal University of Rio Grande do Norte, Av. Campus Universitário, Av. Salgado Filho 3000, Lagoa Nova, Natal CEP59078-970, RN, Brazil

Abstract

In the development of electrochemical sensors, carbon micro-structured or micro-materials have been widely used as supports/modifiers to improve the performance of bare electrodes. In the case of carbon fibers (CFs), these carbonaceous materials have received extensive attention and their use has been proposed in a variety of fields. However, to the best of our knowledge, no attempts for electroanalytical determination of caffeine with CF microelectrode (µE) have been reported in the literature. Therefore, a homemade CF-µE was fabricated, characterized, and used to determine caffeine in soft beverage samples. From the electrochemical characterization of the CF-µE in K3Fe(CN)6 10 mmol L−1 plus KCl 100 mmol L−1, a radius of about 6 µm was estimated, registering a sigmoidal voltammetric profile that distinguishes a µE indicating that the mass-transport conditions were improved. Voltammetric analysis of the electrochemical response of caffeine at the CF-µE clearly showed that no effects were attained due to the mass transport in solution. Differential pulse voltammetric analysis using the CF-µE was able to determine the detection sensitivity, concentration range (0.3 to 4.5 µmol L−1), limit of detection (0.13 μmol L−1) and linear relationship (I (µA) = (11.6 ± 0.09) × 10−3 [caffeine, μmol L−1] − (0.37 ± 0.24) × 10−3), aiming at the quantification applicability in concentration quality-control for the beverages industry. When the homemade CF-µE was used to quantify the caffeine concentration in the soft beverage samples, the values obtained were satisfactory in comparison with the concentrations reported in the literature. Additionally, the concentrations were analytically determined by high-performance liquid chromatography (HPLC). These results show that these electrodes may be an alternative to the development of new and portable reliable analytical tools at low cost with high efficiency.

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Fundação de Amparo à Pesquisa do Estado de São Paulo (Brazil), FAPESP

CNPq Process

Publisher

MDPI AG

Subject

General Materials Science

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