This review presents a critical and comparative analysis of carbon-based electrochemical sensing platforms for the determination of heavy metal ions in water, with emphasis on Pb²⁺, Cd²⁺, and Hg²⁺. The growing discharge of industrial and mining effluents has led to persistent contamination of aquatic environments by toxic metals, creating an urgent need for sensitive, rapid, and field-deployable analytical technologies. Carbon-based nanomaterials, including graphene, carbon nanotubes (CNTs), and MXene, have emerged as key functional components in modern electrochemical sensors due to their high electrical conductivity, large surface area, and tunable surface chemistry. Based on reported studies, typical detection limits for Pb²⁺ and Cd²⁺ using differential pulse voltammetry (DPV) on glassy carbon and thin-film electrodes are in the range of 0.4–1.2 µg/L. For integrated thin-film sensing systems, limits of detection of 0.8–1.2 µg/L are commonly achieved. MXene-based platforms further enhance sensitivity and enable Hg²⁺ detection with linear response ranges typically between 1 and 5 µg/L, accompanied by clear electrochemical or optical signals. Beyond conventional electrochemical detection, this review specifically highlights self-sustaining visual sensors based on MXene integrated with enzyme-driven bioelectrochemical systems, such as glucose oxidase (GOD) and Prussian blue (PB) assembled on ITO substrates. These systems convert chemical energy into measurable colorimetric signals without external power sources, enabling direct visual identification of Hg²⁺ ions. Under optimized conditions (e.g., 5 mg/mL GOD and 5 mM glucose), stable and distinguishable color responses are achieved for rapid on-site monitoring. Overall, this review not only summarizes current performance benchmarks of carbon-based sensors but also identifies key challenges, including long-term stability, selectivity under multi-ion interference, and large-scale device integration, while outlining future directions toward portable multisensor water-quality monitoring systems.

This paper investigates the potential use of coked sands, a byproduct of the thermal processing (pyrolysis) of oil sands, in asphalt concrete mixtures. After pyrolysis extracts the oil from the oil sand, the remaining mineral part becomes coked and changes color to black as solid waste, resulting in a coating of biochar. The coked sand’s X-ray phase analysis (XRD) shows peaks at 4.2564, 3.6749, 3.3768, 3.2380, 3.1903, 2.4581, 2.2800, and 2.2365. Quartz, aluminosilicates, metal oxides, and possibly even carbonates make up the sand’s mineral makeup, as indicated by these peaks. One way to use them is in road construction. In this study, we substituted sand screenings with coked sand in amounts of 5%, 7%, and 10% to examine its impact on the composition of asphalt concrete. This study used 5% paving bitumen (BND 70/100) as a binder for asphalt mineral materials of varying sizes. It concludes that using coked sand to produce asphalt concrete can save 5–10% of sand screenings. The test results showed that adding 5% and 7% of coked sand increases the compressive strength at 50 °C by 8% and 31%, respectively. Adding 10% of coked sand does not increase the strength and actually makes it weaker. The results of the asphalt concrete samples meet type B grade 1 standards of ST RK 1225-2019.

In this study, the oxidative upgrading of heavy oil residues using polymer-containing waste for the sustainable production of bitumen was investigated. Oxidation was performed at temperatures of 250–270 °C for 3–4 h with the addition of 2–3 wt.% polyethylene-based waste, under an air flow of 7 L/min. The physical and mechanical characterization of the resulting bitumen demonstrated compliance with oxidized modified bitumen grades OMB 100/130 and OMB 70/100. FTIR spectroscopy revealed the formation of carbonyl and sulfoxide functional groups, indicating the effective oxidative transformation of the bitumen matrix and partial incorporation of polyethylene fragments. NMR spectroscopy confirmed increased aromaticity and carbonyl content, while also detecting polyethylene-derived signals, suggesting compatibility and integration of the polymer waste into the oxidized structure. The thermal and rheological results showed that the optimal conditions for producing high-quality oxidized bitumen involved the use of 2% polymer waste at 270 °C for 4 h, yielding enhanced physical properties and chemical stability. These findings support the feasibility of using polymer-containing waste for bitumen upgrading, offering both environmental and technical advantages. The method not only improves the quality of bitumen but also contributes to waste valorization and circular economy practices in the road construction industry.

To meet global demand, pesticides play a very important role in the control of pests that damage agricultural products. However, overuse of pesticides threatens ecosystems and human health. In recent years, gas chromatography, liquid chromatography, gas chromatography-mass spectrometry, liquid chromatography-mass spectrometry, capillary chromatography and capillary electrophoresis have been used in the determination of pesticides. Although these methods are highly specific, highly selective and sensitive, the high value of sophisticated laboratory equipment and tools is a complex and time-consuming process. Because of this, electrochemical sensors and biosensor platforms have become good analytical methods for detecting pesticides due to a number of advantages, including ease of detection of system manufacturing processes, high sensitivity and selectivity. This article describes the methods of manufacturing portable electrochemical sensors for detecting pesticide residues in fruits and vegetables on site, that is, the achievements in recent years in the field of cyclic voltammetry, square wave voltammetry, differential pulse voltammetry and electrochemical impedance spectroscopy. In addition, detailed information is provided on the basic mechanism and electrochemical sensitivity of these methods. The development of electrochemical methods and real-time monitoring of smartphone technologies, as well as their integration with detection platforms, are discussed. For readers with a scientific and technological focus, this article will provide additional valuable information for understanding the creation of portable electrochemical devices, rapid detection of pesticides, the role of electrochemical sensitive methods and contributing to their further development.

In this study, a high molecular weight epoxy resin (ELM-NG 900Z) based on diglycidyl ether of bisphenol A was cured with different types of hardeners to examine their impact on the physical and mechanical properties of the epoxy resin. The hardeners used were G-5022X70 (140-170 mg KOH/g), G-A0533 (310-350 mg KOH/g), and G-0930 (280-320 mg KOH/g). The results indicated that the hardener G-A0533 provided the best mechanical properties for the epoxy resin compared to other hardeners. Furthermore, various additives including silica fume, talc, barium sulfate, ferric oxide, and pigments were mixed with the epoxy resin in the presence of the hardener G-A0533 to enhance its mechanical properties. It was observed that the addition of 3% silica fume, 10% ferric oxide, and 3% inorganic pigments improved the mechanical properties, while the addition of 5% talc decreased most mechanical properties and only increased hardness. The incorporation of barium sulfate into the epoxy resin enhanced adhesion and flexural strength but decreased tensile strength and hardness. The inclusion of organic pigment had no significant effect on the mechanical properties of the epoxy resin. This enhancement in mechanical properties is attributed to the type of hardener used as well as the types and amounts of additives mixed with the epoxy resin.

The development of low-cost and highly sensitive electrochemical sensing platforms for pesticide monitoring has attracted significant attention in recent years. In this study, coke-derived carbon (CDC) was successfully synthesized from petroleum coke through high-temperature carbonization under a nitrogen atmosphere. Subsequently, a CDC@CuO-NP nanocomposite was fabricated by depositing copper oxide nanoparticles onto the CDC matrix. The morphology, structure, and elemental composition of the synthesized materials were characterized using scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), and elemental mapping analyses, confirming the successful formation of the composite and the uniform distribution of CuO nanostructures on the carbon surface. Electrochemical characterization demonstrated that the incorporation of CuO significantly enhanced the electrochemical performance of CDC by increasing the electroactive surface area and facilitating electron transfer. The CDC@CuO-NP-modified glassy carbon electrode was applied for the electrochemical detection of dichlorvos (DDVP) using electrochemical impedance spectroscopy (EIS). The sensor exhibited a concentration-dependent increase in charge-transfer resistance and showed a linear response in the concentration range of 247–3770 nM, with the regression equation y = 47.1458C + 111.8162 and a correlation coefficient of R² = 0.9832. The developed sensor achieved a low limit of detection (LOD) of 2.3 nM, demonstrating high sensitivity toward DDVP. These results indicate that the CDC@CuO-NP nanocomposite is a promising, low-cost, and efficient electrode material for the sensitive determination of organophosphorus pesticides and has considerable potential for environmental monitoring and food safety applications.