In this study, we systematically study the efficient production method and electrochemical characteristics of activated carbons (AC) derived from rice husk (RH) and walnut shell (WS). In particular, the effectiveness of physical activation using carbon dioxide (CO₂) was investigated and compared with the more common chemical activation method using potassium hydroxide (KOH). The results show that the KOH–activated samples have remarkable specific capacities, reaching 157.8 F g⁻¹ for RH and 152 F g⁻¹ for WS at 1 A g⁻¹. However, the rate capability of AC obtained via KOH decreases significantly as the scanning rate increases, retaining only 51.5% and 68% of their original capacities for RH–KOH and WS–KOH, respectively, at 20 A g^–1. In contrast, CO₂–activated samples show a superior rate performance with a capacity retention of 75.6% for WS and 80% for RH at the same current density. In addition, electrochemical impedance spectroscopy (EIS) analysis shows that AC obtained via CO₂ has a lower charge transfer resistance compared to its KOH counterparts. CO₂–activated RH and WS electrodes show Rct values of 0.1 Ω and 0.24 Ω, respectively, indicating improved ion transport kinetics and surface area utilization. These results highlight the importance of activation techniques in tailoring the electrochemical behavior of biomass–derived carbon. This study not only expands the understanding of the interaction between activation, morphology, and performance but also indicates the potential of CO₂ activation as an environmentally friendly and efficient alternative. As the field of sustainable energy storage advances, this work provides valuable guidance for the development of high–performance supercapacitor electrodes with less environmental impact.

The thermal decomposition of an ammonium dinitramide-based energetic compound was conducted for the first time using a dispersive inductively coupled plasma mass spectrometer, DTA-TG analysis, and pyrolysis at a constant temperature. A liquid droplet was injected over synthesized CuO catalytic particles deposited on lanthanum oxide-doped alumina. The thermal behavior of the ADN liquid monopropellant revealed that decomposition in the presence of catalytic particles occurs in two distinct steps, with the majority of ejected gases being detected in real-time analysis using the DIP-MS technique. At a temperature of 280 °C, pyrolysis confirmed the catalytic decomposition behavior of ADN, which occurred in two distinct steps.

This study explores the sorption capacity and field application of activated carbons (ACs) derived from plant residues for the remediation of oil-contaminated soils. ACs were prepared from rice husks, reed stalks, pine sawdust and wheat straw using two-stage pyrolysis and chemical activation with potassium hydroxide. The structural and physicochemical properties of these ACs were analyzed using BET surface area measurements, SEM analysis, Raman spectroscopy and FTIR spectroscopy. Sorption experiments at room temperature demonstrated that AC from rice husks (OSL) exhibited the highest sorption capacities for gasoline, kerosene and diesel fuel, with values of 9.3 g/g, 9.0 g/g and 10.1 g/g, respectively. These results are attributed to the well-developed microporous and mesoporous structures of OSL, as confirmed by SEM images and a BET surface area of 2790 m²/g. Field tests conducted at the “Zhanatalap” oil deposit showed that the ACs effectively reduced the oil content in contaminated soils from 79.2 g/kg to as low as 2.6 g/kg, achieving a purification degree of up to 67% within 16 days. This study highlights the critical role of structural properties, such as porosity and graphitization degree, in enhancing the sorption efficiency of ACs.

This paper presents experimental results for the thermal decomposition of hydroxylammonium nitrate (HAN) in the presence of activated carbon with a high specific surface (up to 3000 m2/g) obtained by...

Aluminum–carbon nanotube (Al–CNT) composites represent a cutting-edge class of materials characterized by their exceptional mechanical, thermal, and electrical properties, making them highly promising for aerospace, automotive, electronics, and energy applications. This review systematically examines the impact of various fabrication methods, including conventional powder metallurgy, diffusion and reaction coupling, as well as adhesive and reaction bonding on the microstructure and performance of Al–CNT composites. The analysis emphasizes the critical role of CNT dispersion, interfacial bonding, and the formation of reinforcing phases, such as Al₄C₃ and Al₂O₃, in determining the mechanical strength, wear resistance, corrosion resistance, and thermal stability of these materials. The challenges of CNT agglomeration, high production costs, and difficulties in controlling interfacial interactions are highlighted alongside potential solutions, such as surface modifications and reinforcement strategies. The insights presented aim to guide future research and innovation in this rapidly evolving field.