Carbon nanomaterials are an emerging class of nano-reinforcements to substitute for metal-based nanomaterials in polymer matrices. These metal-free nano-reinforcement materials exhibit a high surface area, thermal stability, and a sustainable nature. Compared to conventional reinforcements, nano-carbon-reinforced polymer composites provide enhanced mechanical and thermal properties. While previous reviews summarized the functionality of nanocomposites, here, we focus on the thermomechanical properties of nano-carbon-reinforced nanocomposites. The role of carbon nanomaterials, including graphene, MXenes, carbon nanotubes, carbon black, carbon quantum dots, fullerene, and metal–organic frameworks, in polymer matrices for the enhancement of thermal and mechanical properties are discussed. Different from metal-based nanomaterials, carbon nanomaterials offer high specific strength, abundance, and sustainability, which are of considerable importance for commercial-scale applications.

Aerogels, due to their unique features like lightweight, ultra-low thermal conductivity, and design variations, have gotten a lot of interest in thermal insulation, photocatalysis, and protective areas. Besides their superior thermal properties, aerogel thermal insulation and photocatalyst materials also possess many inherent flaws, such as handling issues, high manufacturing costs, and low strength as well as toughness. The most persuasive and successful ways to improve photocatalytic and thermal insulating qualities while lowering costs are composition optimization and microstructure reconstruction. Their high surface area and porosity make them ideal for enhancing the efficiency and capacity of these devices. Research may lead to more efficient and longer-lasting energy storage solutions. This review describes the characteristics, microstructural reconstruction, design variation, and properties of all aerogel fabrication techniques and provides a comprehensive overview of scientific achievements linked to them. The effectiveness of raw material compositions, properties, and mechanical parameters are also discussed. The major goal of this review is to highlight the aerogel-based materials and design variations and to explore the most potential development trends for photocatalysis and thermal applications. The industrial as well as technical applications of silica aerogels are also highlighted. This review highlights futuristic applications of aerogel-based textile materials to alleviate the CO₂ burden on our atmosphere, either by providing next-level thermal insulation or by employing them in CO₂ mitigating technologies such as CO₂ capture.

Depletion of oil and gas resources is a major concern for researchers and the global community. Researchers are trying to develop a way to overcome these issues using the Fischer–Tropsch synthesis (FTS) process. The FTS reaction converts a mixture of hydrogen and carbon monoxide gases into a liquid fuel. The reactions are performed in the reactor and in the presence of a catalyst. A series of catalysts, such as iron, cobalt, nickel, and ruthenium, have been used for the FTS process. In iron-based catalysts, the Fe₅C phase is the active phase that produces C₅₊ hydrocarbons. At higher conversion rates, the presence of water in the products is a problem for cobalt catalysts because it can trigger catalyst deactivation mechanisms. Ni-based catalysts play key roles as base catalysts, promoters, and photothermal catalysts in FTS reactions to produce different useful hydrocarbons. Ruthenium catalysts offer not only high activity but also selectivity toward long-chain hydrocarbons. Moreover, depending on the Ru particle size and interaction with the oxide support, the catalyst properties can be tuned to enhance the catalytic activity during FTS. The detailed reaction pathways based on catalyst properties are explained in this article. This review article describes the issues and challenges associated with catalysts used for the FTS process.

The zinc oxide nanoparticles (ZnO NPs) and surfactants that are widely used in commercial and industrial products lead to the likelihood of their co-occurrence in natural water, making it essential to investigate the effect of surfactants on the fate and mobility of ZnO NPs. The present study seeks to elucidate the effect of an anionic sodium dodecyl sulfate (SDS) and a nonionic nonylphenol ethoxylate (NPEO), on ZnO NPs adsorption, aggregation, dissolution, and removal by the coagulation process. The results indicate that the presence of SDS in ZnO NPs suspension significantly reduced the ζ-potential and hydrodynamic diameter (HDD), while the effect of NPEO was found not to be significant. The sorption of SDS and NPEO by ZnO NPs were fitted with Langmuir model, but the Freundlich isotherm was more suitable for SDS at pH 9.0. Moreover, the adsorption was strongly pH-dependent due to the formation of mono-bilayer patches onto the NPs. The SDS remarkably affect the dissolution and aggregation phenomena of ZnO NPs in natural waters as compared to NPEO. Finally, the coagulation results showed that the removal efficiency of ZnO, Zn²⁺ and the surfactant in synthetic and wastewaters at optimum ferric chloride (FC) dosage reached around 85–98% and 20–50%, respectively. Coagulation mechanism investigation demonstrated that the cooperation of charge neutralization and adsorptive micellar flocculation (AMF) might play an important role. In summary, this study may provide new insight into the environmental behavior of coexisting ZnO NPs and surfactants in water treatment processes, and it may facilitate their sustainable use in commercial products and processes.

The purpose of this study is to control the viscous behavior of lightweight aggregates through the chemical design of a lightweight aggregates material in order to solve the problem of the adhesion of lightweight aggregates by viscous behavior in the bloating activation temperature range of lightweight aggregates. In order to induce a reduction of Fe₂O₃ inside the aggregates, Fe₂O₃ and carbon were added to acid clay so as to produce aggregate. The particle density and the water absorption rate of the aggregates were measured, the cross-section was observed with an optical microscope, and the distribution of hematite of the lightweight aggregates was confirmed by a 3D CT analysis. Pilot scale rotary kiln experiments were performed. The optimal additive contents for the production of lightweight aggregates using acid clay were 8–13 wt% of Fe₂O₃ and 2–3 wt% of carbon. The addition of additives decreased the bloating activation temperature, and viscous behavior was promoted in the core portion of the aggregates, resulting in a difference in the melting point between the shell and the core. As a result, the occurrence of adhesion at the aggregates surface was suppressed.