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The 3D photoelectrochemical cell was developed with epoxy resin and a working composite electrode produced with a blend of 3D printer commercial conductive filament of polylactic acid biopolymer and carbon black (PLA/CB) mixed with silica/tungsten (VI) oxide (SiO2/WO3) synthesized was used for the determination of imidacloprid in water samples. Imidacloprid is a neonicotinoid pesticide considered potentially neurotoxic, and investigating its presence in aquatic environments is of great importance. The PLA/CB/SiO2/WO3 sensor was morphologically characterized by scanning electron microscopy. Photoelectrochemical performance of the composite sensor was evaluated by chronoamperometry, electrochemical impedance spectroscopy and cyclic voltammetry. In the presence of light (on) using differential pulse voltammetry in borate buffer solution (0.1 mol L−1, pH 7.0), the modified sensor exhibited a linear range of 0.15–93.70 μmol L−1 and with a limit of detection of 0.04 μmol L−1 to determine imidacloprid. The modified sensor did not present interferences for K+ and Fe3+ ions, carbendazim, glyphosate and thiamethoxam pesticides. Furthermore, the recovery in spiked samples successfully determined the presence of imidacloprid pesticide in tap water and natural river surface water. [ABSTRACT FROM AUTHOR]

Dopamine (DA) is a crucial neurotransmitter in the central nervous system (CNS) of human and multicellular animal brains. In this paper, we report for the first time the synthesis of carbon black (C)/phosphotungstic acid (PWA) composites by doping PWA on carbon black nanoparticles by impregnation method. The synthesized materials were characterized using high‐resolution scanning electron microscopy (SEM), X‐ray diffraction spectroscopy (XRD) and Fourier transform infrared spectroscopy (FT‐IR). Glassy carbon electrodes (GCE) modified by C/PWA composites were used to detect dopamine. The electrochemical redox behavior of DA was studied with cyclic voltammetry (CV). Under optimized conditions, DA was detected by differential pulse voltammetry (DPV) and the calibration plot showed linearity (R2=0.9988) over the range of DA concentrations of 10 μM‐600 μM with a detection limit of 0.1 μM. The sensor's capability to detect DA in commercial DA injections in real time has been successfully demonstrated. [ABSTRACT FROM AUTHOR]

In this work a comparative study of Screen‐Printed Carbon Electrodes (SPCE) – bare and modified by drop casting with carbonaceous nanomaterials (CNMs) as Multi Walled Carbon Nanotubes (MWCNT), Carbon Black and Functionalized Carbon Black for voltammetric determination of 5‐methyl‐6‐nitro‐7‐oxo‐4,7‐dihydro‐1,2,4‐triazolo[1,5‐a]pyrimidinide l‐arginine monohydrate (Triazid) as a potential drug with a broad spectrum of antiviral activity is reported. Bare SPCE and CNMs modified SPCE (SPCE/CNMs) have been characterized morphologically by SEM and electrochemically by cyclic voltammetry/electrochemical impedance spectroscopy with [Fe(CN)6]4−/3− as redox probe. Significant improvement of electrochemical performances is achieved with SPCE/CNMs compared with the bare SPCE. Among SPCE/CNMs studied SPCE modified with MWCNT (SPCE/CNT) is characterized by the best combination of electrochemical properties and electroanalytical performance towards TD. The linear dynamic range is 25–200 mg L−1 (R2=0.9975) with the limit of detection – 2.8 mg L−1 Triazid using SPCE/CNT and Square‐Wave Voltammetry technique. The developed sensor was successfully used for Triazid determination in the Pharmaceutical Substance "TRIAZID". The results achieved with SPCE/CNMs after chemical binding of dissolved oxygen in 0.04 M Britton‐Robinson buffer+0.04 M Na2SO3 (pH 7.2±0.2) are very useful for further development of cost‐effective and time‐consuming pharmaceutical routine assay. [ABSTRACT FROM AUTHOR]

Electrochemical sensors to quantify concentrations of emerging pollutants have attracted great attention from the industry and scientific community. Nanomaterials such as carbon black have been applied in sensors to identify substances that are toxic to the environment and human health due to their excellent electroanalytical properties. The aim of the study was to develop a novel electrochemical sensor for the endocrine disruptor hormone determination. To our knowledge, for the first time the synthesis of material based on carbon black containing immobilized palladium nanoparticles, with the application for the hormone ethinylestradiol, is reported in the literature. The material was synthesized, characterized, and applied to the determination in tap water and human urine of the synthetic hormone 17α‐ethinylestradiol (EE2), which is currently considered an emerging pollutant. The morphology, structure and electrochemical performance of the sensors were characterized by scanning electron microscopy (SEM) and cyclic voltammetry (CV). Differential pulse voltammetry (DPV) in sodium phosphate buffer solution at pH 5.0 allowed the generation of a method to quantify the concentration of 17α‐ethinylestradiol in a linear range of 0.5–119.0 μmol L−1, obtaining 81.0 nmol L−1 of calculated limit of detection (LOD). The system was efficient in detecting 17α‐ethinylestradiol in real urine samples and showed no interferences for ascorbic acid, uric acid, progesterone, and dopamine. It is noteworthy that the results obtained showed good recovery values, considering that the urine samples were not previously treated or pre‐concentrated, which suggests the development of an electrochemical sensor that works in situ and in real time to monitor relevant substances in the control clinical and environmental, with the possibility of point‐of‐care analyses. [ABSTRACT FROM AUTHOR]

This paper reports the development of a simple electroanalytical method for imazethapyr (IMT) determination in rice samples based on molecularly imprinted polymer and functionalized carbon black paste electrode (MIP‐fCBPE). Carbon black (CB) was functionalized by the insertion of oxygenated functional groups upon acid treatment with HNO3 and H2SO4. The functionalized carbon black (fCB) presented higher performance for IMT determination than the CB without functionalization. The insertion of molecularly imprinted polyvinylimidazole (MIP‐VN) in the fCBPE promoted a significant increase in the cathodic peak current even at low proportions (7.5 % w/w) due to the specific binding sites for IMT recognition. For IMT determination, DPV parameters were optimized by the Doehlert matrix applying 0.1 V for 60 s as pre‐treatment in acetate buffer solution (pH 3.0) as supporting electrolyte. The proposed method showed low limit of detection (0.03 μmol L−1), a wide linear range (0.10–70.00 μmol L−1), and good precision in terms of repeatability of intraday measures (RSD%=3.6). The method was applied in rice samples after microwave‐assisted extraction of IMT and the accuracy of the method was evaluated by addition/recovery assays (96.3–105.7 %), being statistically attested using HPLC‐DAD as reference technique. [ABSTRACT FROM AUTHOR]

Glyceline, reline, or ethaline deep eutectic solvents and carbon black nanoparticles within a crosslinked chitosan film are investigated as glassy carbon electrode modifiers for the first time. The selected 5 mgmL-1 glyceline modified GCE was characterized by cyclic voltammetry, electrochemical impedance spectroscopy, and scanning electron microscopy. Simultaneous determination of acetaminophen and diclofenac by differential pulse adsorptive stripping voltammetry (DPAdSV) presented limits of detection of 2.6×10-8 and 5.2× 10-8 molL-1 for acetaminophen and diclofenac, respectively, in pharmaceutical and biological samples. The obtained results were compared with those obtained by HPLC at a confidence level of 95%. [ABSTRACT FROM AUTHOR]

Herein, we demonstrated miniature solid‐contact ion‐selective electrodes (ISEs) using a commercial mesoporous carbon black (MCB) as ion‐to‐electron transducer. MCB is attractive in its high surface area, good conductivity, relative low cost and availability. ISEs for potassium (K+) and nitrate (NO3−) ions were prepared by subsequently coating the sealed glass capillaries (1.5 mm) with MCB and ion‐selective membranes. Addition of MCB substantially stabilized electrode response by providing adequate double‐layer capacitance and lowering resistance by more than 100× compared to the coated‐wire electrodes. The electrodes exhibited near‐Nernstian slopes of 59.6 (K+ ionophore), 57.8 (K+ ion‐exchanger) and −54.8 (NO3− ion‐exchanger) with standard solutions in the range of 10−5 to 10−1 M. Fast response (∼10 s) and reproducible sensitivities were also obtained in a mixed electrolyte containing interfering ions, although with a baseline drift of 2–10 mV/day in the long term. Importantly, the electrodes can be simply stored in air between measurements and used directly without conditioning in solutions. With simple fabrication and free maintenance, these sensors offer a low cost and convenient alternative to bulk ISEs, especially when sample volumes or space are limited. [ABSTRACT FROM AUTHOR]