One of the goals of this research was to develop an electrochemical sensor that had the ability to determine the target analyte and was both cheap and non-toxic. Another goal was to influence the reduction of electronic waste. In accordance with these, a graphite rod from zinc-carbon batteries was used to prepare an electrochemical sensor for the determination of L-tryptophan in Britton–Robinson buffer solution. Two electrochemical methods were used in the experimental research, differential pulse voltammetry and cyclic voltammetry. The effect of different parameters, including the pH value of supporting solution, scan rate, as well as the concentration of L-tryptophan on the current response, was studied. The pH value of Britton–Robinson buffer influenced the intensity of L-tryptophan oxidation peak, as well as the peak potential. The intensity of the current response was the highest at pH 4.0, while the peak potential value became lower as the pH increased, indicating that protons also participated in the redox reaction. Based on the obtained data, electrochemical oxidation of L-tryptophan at the graphite electrode was irreversible, two electron/two proton reaction. In addition, it was observed that the oxidation peak increased as the scan rate increased. According to the obtained electrochemical data, it was suggested that the oxidation of L-tryptophan was mixed controlled by adsorption and diffusion. The linear correlation between oxidation peak and L-tryptophan concentration was investigated in the range 5.0–150.0 µM and the obtained values of limit of detection and limit of quantification were 1.73 µM and 5.78 µM, respectively. Also, the prepared electrochemical sensor was successful in determination of target analyte in milk and apple juice samples.

The determination of target analytes at very low concentrations is important for various fields such as the pharmaceutical industry, environmental protection, and the food industry. Caffeine, as a natural alkaloid, is widely consumed in various beverages and medicines. Apart from the beneficial effects for which it is used, caffeine also has negative effects, and for these reasons it is very important to determine its concentration in different mediums. Among numerous analytical techniques, electrochemical methods with appropriate sensors occupy a special place since they are efficient, fast, and entail relatively easy preparation and measurements. Electrochemical sensors based on carbon materials are very common in this type of research because they are cost-effective, have a wide potential range, and possess relative electrochemical inertness and electrocatalytic activity in various redox reactions. Additionally, these types of sensors could be modified to improve their analytical performances. The data available in the literature on the development and modification of electrochemical sensors for the determination of caffeine are summarized and discussed in this review.

Cadmium is one of the most dangerous pollutants found in the environment, where it exists mainly due to human activities. High cadmium concentrations can cause serious problems, which is why the detection and determination of Cd is one of the most important tasks. Electroanalytical methods provide rapid and accurate results in the detection of cadmium in various solutions. In this study, the possibility of using a bismuth film electrode deposited on a brass surface and electroanalytical techniques for the detection of cadmium is investigated. The bismuth film was deposited on the surface of the brass electrode using a chronoamperometric technique. Cyclic voltammetry and electrochemical impedance spectroscopy were used to characterize the synthesized bismuth film electrode. The current peaks obtained by anodic square-wave stripping voltammetry under optimized conditions showed a linear relationship in the investigated concentration range of cadmium. The study of the interference of different cations (Cr³⁺, Mn²⁺, Zn²⁺, Ca²⁺, K⁺, Mg²⁺ and Na⁺) showed that the tested cations have no influence on the determination of Cd²⁺ ions in the investigated solution. This finding provides a good opportunity for the use of the synthesized electrode in real samples.

Metals stability and corrosion resistance are very important factors that influence the possibility of their applications. In order to study and foresee the behavior of metals during various applications in all kinds of conditions and media, numerous approaches and techniques are developed and applied. Among those techniques, electrochemical measurements nowadays have a dominant role since they are proved to be highly efficient, reliable, fast, relatively low-cost, and easy regarding the preparation and execution of measurements. Besides that, they also provide quite a good amount of data regarding the effect and the mechanism of the reactions that metals interact in. Metals corrosion is reduced by various methods, one of the most frequently used ones is the application of corrosion inhibitors. Usually, organic compounds are studied as potential corrosion inhibitors, and at the moment the focus is on the effect on the environment. Hence, environmentally friendly and non-toxic inhibitors are important research topics. Purines, since they are the group of bioorganic compounds found in numerous biochemical structures such as DNA and RNA, present a very interesting possible solution and are studied as inhibitors of corrosion for copper, steel, aluminum, etc., as well as for some metal alloys. Data obtained and available up until the present are presented and discussed in this review.

Waste from zinc−carbon batteries poses a serious environmental protection problem. One of the main problems is also the reliable and rapid determination of some compounds that may be present in food and beverages consumed worldwide. This study addresses these problems and presents a possible solution for the electrochemical detection of xanthine using carbon from spent batteries. Cyclic voltammetry and differential pulse voltammetry are electrochemical methods used for the detection of xanthine. The techniques used demonstrate the mechanism of xanthine oxidation in the tested environment. A linear correlation was found between the oxidation current peaks and the xanthine concentration in the range of 5·10⁻⁷ to 1·10⁻⁴ M, as well as the values for the limit of detection and the limit of quantification, 7.86·10⁻⁸ M and 2.62·10⁻⁷ M, respectively. The interference test shows that the electrode obtained from waste Zn-C batteries has good selectivity, which means that the electrode can be used for xanthine determination in the presence of various ions. The data obtained show that carbon sensors from used zinc−carbon batteries can be used to detect xanthine in real samples.