We examine the photocatalytic activity (PCA) of ZnO/graphitic carbon nitride g-C₃N₄ (g-CN) composite material for methylene blue (MB) degradation under visible-light irradiation (VLI). The polymeric g-CN materials were fabricated by the pyrolysis of urea and thiourea. More importantly, ZnO/g-CN nanostructured composites were fabricated by adding the different mounts (60, 65, 70, and 75 wt.%) of g-CN into ZnO via the simple hydrothermal process. Among fabricated composites, the 75% ZnO/g-CN nanocomposites displayed a superior PCA for MB degradation, which were ~three-fold an enhancement over the pure ZnO nanoparticles. The fabricated materials have been evaluated by X-ray diffraction (XRD), UV-Vis, Fourier transform infrared (FT-IR) spectroscopy, and electron microscopy. More importantly, the photodegradation of MB could get 98% in ZnO/g-CN could be credited to efficient separation of photo-induced charge carriers between ZnO and g-CN. Also, the recycling efficiency of the as-prepared composites was studied for multiple cycles, which shows that the photocatalysts are stable and suitable to carry out photocatalytic degradation in the logistic mode. Additionally, the probable photocatalytic mechanism has also discussed. The synthetic procedure of ZnO/g-CN based materials can be used in numerous fields such as environmental and in energy storage applications.

Hydrothermally assisted magnetic ZnO/Carbon nanocomposites were prepared using the selective biowaste of pomelo orange. Initially, the carbon aerogel (CA) was prepared hydrothermally followed by a freeze-drying method. Furthermore, the iron oxide nanoparticles were deposited onto the surface of carbon using the co-precipitation method and we obtained magnetic carbon nanocomposite, i.e., Fe₃O₄/C (MNC). Moreover, the ZnO photocatalysts were incorporated onto the surface of MNC composites using a hydrothermal process, and we obtained ZnO/MNC composites. The ZnO/MNC (55%), ZnO/MNC (65%) and ZnO/MNC (75%) composites were prepared by a similar experimental method in order to change the weight ratio of ZnO NPs. Using a similar synthetic procedure, the standard ZnO and Fe₃O₄ nanoparticles were prepared without the addition of CA. The experimental results were derived from several analytical techniques, such as: X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Raman and diffuse reflectance spectroscopy (DRS-UV). The synthesized carbon, ZnO, Fe₃O₄, ZnO/MNC (55%), ZnO/MNC (65%) and ZnO/MNC (75%) composites were examined through the photocatalytic degradation of methylene blue (MB) under visible-light irradiation (VLI). The obtained results revealed that the composites were more active than carbon, ZnO and Fe₃O₄. In particular, the ZnO/MNC (75%) composites showed more activity than the rest of the composites. Furthermore, the recycling abilities of the prepared ZnO/MNC (75%) composites were examined through the degradation of MB under identical conditions and the activity remained constant up to the fifth cycle. The synthetic procedure and practical applications proposed here can be used in chemical industries, biomedical fields and energy applications.

A carbon aerogel (CA)-assisted CdS nanocomposite was prepared by hydrothermal process and was investigated as a photocatalyst towards the photodegradation of methylene blue (MB) dye and colorless phenol under visible light irradiation (VLI). CdS have attracted wide attention due to their relatively narrow band gap for the visible light effect and the suitably negative potential of the conduction band (CB) edge for the neutralization of H⁺ ions. The obtained characterization results suggest that the CA-assisted CdS nanocomposite has enhanced photophysical properties, a more surface area, and the desired morphology at the nm scale. Under optimization, CdS CA 8% shows superior catalytic activity for degradation compared with other samples. The photocatalytic activities of the as-synthesized samples were examined under VLI through the MB and phenol degradation. Compared with pure CA and CdS, the CA (8%)-assisted CdS nanoparticles (NPs) offer significantly enhanced photocatalytic efficiency for MB and phenol. The mechanism of photocatalytic reaction was examined by adding various scavengers, and the results revealed that the holes generated in CA (8%)-assisted CdS NPs have a crucial impact on the visible light photocatalytic process. The improved photocatalytic degradation was due to the strong interaction between the CA and CdS NPs.

γ-valerolactone (GVL) is a crucial chemical feedstock used in the production of fuel additives, renewable fuels, and fine chemicals alternative to petroleum-based solvents and chemicals, supporting the transition to sustainable energy solutions. It is promptly acquired by hydrogenating levulinic acid (LA) in a gaseous or liquid phase with a homogeneous or heterogeneous catalyst using a variety of recognized catalytic processes. Herein, this work focuses on the use of silica-supported copper (Cu/SiO₂) catalysts for the gas-phase hydrogenation of LA to GVL under mild reaction conditions. The study analyzes how copper loading can affect the catalytic activity of the Cu/SiO₂, while the flow rate of LA, time-on-stream, reaction temperature, and LA concentration affect the catalytic efficiency. The SiO₂ support’s various Cu loadings are crucial for adjusting the catalytic hydrogenation activity. One of the studied catalysts, a 5 wt% Cu/SiO₂ catalyst, demonstrated ~81% GVL selectivity with ~78% LA conversion and demonstrated stability for ~8 h while operating at atmospheric pressure and temperature (265 °C) and 0.5 mL/h of LA flow rate. The ability to activate hydrogen, high amount of acidic sites, and surface area were all discovered to be advantageous for increased GVL selectivity.