As a byproduct of emerging as one of the world’s key producers of pharmaceuticals, China is now challenged by the emission of harmful pharmaceutical VOCs. In this review, the catalogue and volume of VOCs emitted by the pharmaceutical industry in China was introduced. The commonly used VOC removal processes and technologies was recommended by some typical examples. The progress of catalytic combustion, photocatalytic oxidation, non-thermal plasma, and electron beam treatment were presented, especially the development of catalysts. The advantages and shortages of these technologies in recent years were discussed and analyzed. Lastly, the development of VOCs elimination technologies and the most promising technology were discussed.

This study develops a semi-empirical model of an alkaline water electrolyzer (AWE) based on thermodynamic and electrochemical principles to investigate cell voltage behavior during electrolysis. By importing polarization curve test data under specific operational conditions, eight undefined parameters are precisely fitted, demonstrating the model’s high accuracy in describing the voltage characteristics of alkaline electrolyzers. Additionally, an AWE system model is introduced to examine the influence of various operational parameters on system efficiency. This innovative approach not only provides detailed insights into the operational dynamics of AWE systems but also offers a valuable tool for optimizing performance and enhancing efficiency, advancing the understanding and optimization of AWE technologies.

Molybdovanadylphosphoric acid (HPMV) was supported on a carbon nitride-modified SBA-15 (CN-SBA-15) molecular sieve to enhance its catalytic performance for oxidation of methacrolein (MAL) to methacrylic acid (MAA). HPMV/CN-SBA exhibited increased catalytic activity (20%) and five times greater MAA selectivity (98.9%) compared to bulk HPMV. HPMV supported on CN-SBA-15 exhibited much better catalytic performance as compared to that on other supports, such as KIT-6, HY zeolite, TiO₂, Al₂O₃, SiO₂, CNTs, and NH₃-modified CNTs. The supported HPMV was well characterized by FT-IR, XRD, SEM, N₂ physical desorption, TG-DTA, NH₃-TPD, CO₂-TPD, XPS, and solid-state NMR. The CN minimized the interaction between the silica support and HPMV. HPMV was successfully separated from SBA-15, which was restricted by CN to increase stability and prevent interaction between the catalysts and support that would lead to decomposition of the catalysts during calcination and reaction. HPMV reacted with amino groups on the CN, which improved MAA selectivity and enhanced the thermal stability of the supported heteropoly acid (HPA) catalysts. This work identifies a new approach to preparing highly efficient and stable supported HPA catalysts for oxidation reactions.