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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]

In this work, a renewable tyrosinase‐based biosensor was developed for the detection of catechol, using a carbon black paste electrode, without any mediator. The effect of pH, type of electrolyte, and amount of tyrosinase enzyme were explored for optimum analytical performance. The best‐performing biosensor in amperometric experiments at potential −0.2 V vs. Ag/AgCl (3 mol L−1 KCl) was obtained using a 0.1 mol L−1 phosphate buffer solution (pH 7.0) as electrolyte. Under optimized conditions, the proposed biosensor had two concentration linear ranges from 5.0×10−9 to 4.8×10−8 and from 4.8×10−8 to 8.5×10−6 mol L−1 and a limit of detection of 1.5×10−9 mol L−1. The apparent Michaelis‐Menten constant (KMMMapp) was calculated by the amperometric method, and the obtained value was 1.2×10−5 mol L−1 whose result was similar when compared with other studies previously. The biosensor was applied in river water samples, and the results were very satisfactory, with recoveries near 100 %. In addition, the response of this biosensor for different compounds, taking into account their molecular structures was investigated and the results obtained showed no interference with the response potential of catechol. The electrochemical biosensor developed in this work can be considered highly advantageous because it does not require the use of a mediator (direct detection) for electrochemical response, and also because it is based on a low‐cost materials that can be used with success to immobilise other enzymes and/or biomolecules. [ABSTRACT FROM AUTHOR]

Towards the development of miniaturised and low‐cost sensors for heavy metals detection in water, herein we describe an electrochemical sensor for the co‐detection of lead and cadmium. The sensor was developed using screen‐printed electrode modified with a composite of poly(propylene imine) dendrimer and carbon black. The electrode was modified by drop casting of the carbon black and electrodeposition of the poly(propylene imine) dendrimer. This modified electrode (sensor) was characterised by cyclic voltammetry and electrochemical impedance spectroscopy, revealing improved electrochemical performances. Square wave anodic stripping voltammetry (SWASV) was used to achieve the simultaneous detection of Pb(II) and Cd(II) at trace level, obtaining satisfactory LOD of 3.6 ppb and 15.3 ppb respectively; and sensitivity of 0.49 μA/ppb and 0.57 μA/ppb in tap water. [ABSTRACT FROM AUTHOR]

Bisphenol A (BPA) is an environmental endocrine disrupting chemical, which can lead to various adverse health effects. Aiming to develop effective tools for the detection of BPA, this work reports a low cost and stable film based on casein (CAS) and Carbon Black (CB). The proposed material (CAS‐CB) showed structures of CAS surrounded by CB agglomerates observed by Scanning Electron Microscopy while Fourier Transform Infrared Spectroscopy analysis illustrated characteristic bands of casein. Cyclic Voltammetry (CV) and linear sweep voltammetry (LSV) were used to investigate the electrochemical behavior of BPA using the CAS‐CB. Under optimal conditions, LSV detection presented a limit of detection of 0.25 μmol L−1 in a linear range from 0.49 to 24 μmol L−1. Additionally, the working electrode (GC) modified by the proposed film (CAS‐CB) was applied for BPA sensing in environmental and milk samples. The results showed recoveries between 95.4 to 114 % attesting the efficiency of this new material, which has simplicity in the preparation, high conductivity, and adsorption capability. [ABSTRACT FROM AUTHOR]

The antidiabetic drug metformin (MET) is one of a group of emerging pharmaceutical drug contaminants in the wastewater treatment plants. The electrochemical behaviour of MET−Cu(II) complex by differential pulse and square wave voltammetry, in a wide pH range, at a glassy carbon electrode modified with a carbon black dihexadecylphosphate film (CB−DHP/GCE), was investigated. The MET−Cu(II) complex oxidation showed one pH‐dependent process, which leads to the formation of an oxidation product, being oxidized at a lower potential. The electroanalytical MET−Cu(II) complex detection limit, LOD=0.63 μM, and quantification limit, LOQ=2.09 μM, were obtained, and the MET−Cu(II) complex determination in wastewater samples collected from a senior residence effluent, using the CB−DHP/GCE, was achieved. Considering MET toxicity, the electrochemical evaluation of MET−dsDNA interaction, in incubated solutions and using dsDNA‐electrochemical biosensors, following the changes in the oxidation peaks of guanosine and adenosine residues electrochemical currents, was also investigated. The MET−dsDNA interaction mechanism, for shorter times, occurs by the binding of MET molecules in the minor grooves of the dsDNA, and for long times, the stabilization of the MET−dsDNA complex, causing a local distortion and/or unwinding of dsDNA morphology, is described. However, MET did not promote DNA oxidative damage. [ABSTRACT FROM AUTHOR]

The paper reports the development of a new sensor based on Printex L6 (CPL6) carbon black modified with copper oxides (CuO/Cu2O) nanoparticles and its application towards the determination of Propylparaben (PP). In fact, it is the first report of its kind in the literature. The sensor was produced through the dispersion of CPL6 in dimethylformamide on glassy carbon electrode surface followed by CuO/Cu2O electrodeposition. The conditions of electrodeposition investigated included time and solution concentration of Cu (II). Morphological, structural and electrochemical characterizations of the sensor were performed. Under optimal conditions, wide linear range (1.0 to 35.0 μmol L−1) was obtained in the detection of PP. The detection limit obtained was 0.46 μmol L−1 (S/N=3). The CuO/Cu2O‐CPL6/GCE sensor was found to be as sensitive as the high performance liquid chromatography in the determination of PP in both cosmetic and river water samples, in addition to being reproducible and stable. [ABSTRACT FROM AUTHOR]

Abstract: Detection of traces from pharmaceutical drugs such as antibiotics in drinking water and foodstuff is essential for guaranteeing human health in some environments, and this has to be done with low cost technologies to be widely deployed in public services and industry. In this paper, we describe an ultralow cost (

Abstract: Synthesis of nanomaterials using cheap and highly efficient material is an important aspect of nanotechnology. In this present work, we have used the carbon black (CB) as a highly conductive and inexpensive carbonaceous material for the fabrication of the electrochemical sensor. However, the poor dispersion in water obstructs the usage of CB in electrochemical sensor and biosensor applications. Hence, the CB was functionalized by simple reflux method and the functionalized CB (f‐CB) nanospheres hybrids with hydrothermally synthesized MoS2 nanoclusters by simple ultrasonication process. In addition, the various suitable spectrometric techniques used to probe the surface morphology and chemical modification of the prepared materials. The prepared MoS2 and f‐CB nanohybrids (f‐CB/MoS2) applied for the electrocatalytic reduction of toxic chloramphenicol (CAP). Fascinatingly, the f‐CB/MoS2 modified electrode showed a competitive electrocatalytic performance comparing with other modified electrodes. At the optimized condition, the sensor exhibited the LOD about 0.002 μM, wider linear range 0.015 to 1370 μM with the sensitivity of 3400 μA μM−1 cm−2 for the determination of CAP. Moreover, the practical viability of the sensor was exploited in milk powder and honey samples. [ABSTRACT FROM AUTHOR]

Electrochemical sensor has been proposed on the base of glassy carbon electrode (GCE) modified with carbon black (CB) and pillar[5]arene (P[5]A). The characteristics of the peak currents were found to be sensitive to the incubation of the sensor in organic acid and DNA solution. The detection of n×(10−8-10−5) M of organic acid and down to (1-5)×10−18 g of DNA was attributed to the effect of the analytes on the aggregation and relative stability of oxidized and reduced forms of P[5]A. No signal interference with the alkali and alkali-earth metal ions was found. The electrochemical sensor was tested in the detection of specific DNA interactions, i.e. reactive oxygen species damage and intercalating pharmaceuticals detection. [ABSTRACT FROM AUTHOR]

In this work, a simple and highly selective voltammetric method was developed for the simultaneous determination of paracetamol (PCT) and codeine (COD) in pharmaceuticals and human body fluids employing a glassy carbon electrode modified with carbon black (CB) and nickel oxide nanoparticles (NiONPs) within a dihexadecylphosphate (DHP) film. Using square-wave voltammetry (SWV), a separation of ca. 550 mV between the oxidation peak potentials of PCT and COD was obtained. The simultaneous determination of PCT and COD presented a linear concentration range from 3.0 to 47.8 µmol L−1 for PCT and from 0.83 to 38.3 µmol L−1 for COD. [ABSTRACT FROM AUTHOR]

In this work a comparative study using Screen-Printed Electrodes (SPEs) modified by drop casting with Carbon Black, Single Walled Carbon NanotubesCOOH, Graphene Oxide, and reduced Graphene Oxide is reported. The carbon nanomaterials employed were characterized by X-ray photoelectron and Raman spectroscopy, while the modified SPEs have been morphologically and electrochemically characterized. Nanoengineered SPEs have been tested with ferricyanide, NADH, ascorbic acid and cysteine. We observed valuable electroanalytical performances of Carbon Black with the advantage to be i) cost-effective ii) suitable to obtain stable and homogenous dispersion and iii) mass-producible following a well established route. [ABSTRACT FROM AUTHOR]

Both screen-printed electrodes modified with a dispersion of carbon black (CB) and solid paste electrodes prepared using a nanostructured CB were developed and characterized. Indeed, increasing the peak currents and/or their shifting to negative potentials were observed, exhibiting efficient electrocatalytic activity towards nitrite oxidation with high sensitivity and low detection limit. Solid carbon paste electrodes (SCPEs) and solid carbon black paste electrodes (SCBPEs) were challenged in amperometric mode with nitrite since detection limit reached is 65 and 5 nM respectively. Nitrate was first reduced to nitrite in reductor column, then detected on SCBPEs. Nitrate and nitrite were determined in real samples. [ABSTRACT FROM AUTHOR]