Cyanide gas is highly toxic and volatile and is among the most typical toxic and harmful pollutants to human health and the environment found in industrial waste gas. In the military context, cyanide gas has been used as a systemic toxic agent. In this paper, we review cyanide gas elimination methods, focusing on adsorption and catalysis approaches. The research progress on materials capable of affecting cyanide gas adsorption and catalytic degradation is discussed in depth, and the advantages and disadvantages of various materials are summarized. Finally, suggestions are provided for future research directions with respect to cyanide gas elimination materials.

A novel BiOI/TiO₂ nano-heterojunction was prepared using hydrothermal and sol-gel methods. The composite material was characterized by X-ray diffraction, ultraviolet-visible diffuse reflection spectroscopy, scanning electron microscopy, and transmission electron microscopy. The crystallinity and response to light of BiOI/TiO₂ were controlled by preparation conditions such as the optimal solvent condition and heat treatment temperature. The photocatalytic activity of the BiOI/TiO₂ catalyst was examined using benzene as a test molecule. The benzene degradation rate of the composite catalyst under visible light was enhanced compared to pure TiO₂, thus reaching 40% of the original benzene concentration, which increased further to >60% after surface acidification. The fluorescence spectra, light current, and electron paramagnetic resonance confirmed that the enhanced activity was attributed to carrier separation by the heterojunction. The acid sites and active chlorine of hydrochloric acidification offer a novel mechanism for photocatalytic reactions.

Thermocatalytic decomposition is an efficient purification technology that is potentially applicable to degrading chemical warfare agents and industrial toxic gases. In particular, ZrO₂ has attracted attention as a catalyst for the thermocatalytic decomposition of dimethyl methylphosphonate (DMMP), which is a simulant of the nerve gas sarin. However, the influence of the crystal phase and morphology on the catalytic performance of ZrO₂ requires further exploration. In this study, monoclinic- and tetragonal-phase ZrO₂ (m- and t-ZrO₂, respectively) with nanoparticle, flower-like shape and hollow microsphere morphologies were prepared via hydrothermal and solvothermal methods, and their thermocatalytic decomposition of DMMP was systematically investigated. For a given morphology, m-ZrO₂ performed better than t-ZrO₂. For a given crystalline phase, the morphology of hollow microspheres resulted in the longest protection time. The exhaust gases generated by the thermocatalytic decomposition of DMMP mainly comprised H₂, CO₂, H₂O and CH₃OH, and the by-products were phosphorus oxide species. Thus, the deactivation of ZrO₂ was attributed to the deposition of these phosphorous oxide species on the catalyst surface. These results are expected to help guide the development of catalysts for the safe disposal of chemical warfare agents.

Here, we report a highly efficient and stable catalytic system based on monometallic oxides supported on HY zeolites for the catalytic oxidation of chlorobenzene (CB). Among the transition and rare-earth metal oxides screened, the 30Cu/HY catalyst demonstrates exceptional performance, achieving near 100% CB conversion at 300 °C (500 ppm CB, 10,000 h⁻¹) alongside outstanding 24 h continuous stability without deactivation. Quantitative Py-IR analysis reveals that this superior activity is fundamentally driven by extensive solid-state ion exchange, forming robust Lewis acid centers (Cu-Y structures) that synergize with zeolitic Brønsted acid sites to efficiently polarize and cleave C-Cl bonds. Through an integrated approach combining in situ DRIFTS, real-time mass spectrometry, TGA, and NLDFT pore size analysis, we elucidate that the exceptional deep-oxidation capability of Cu/HY continuously mineralizes carbonaceous intermediates. This property minimizes coke deposition (2.91 wt%) and preserves the hierarchical pore architecture, preventing the coverage of active sites and severe pore blockage by partially oxidized intermediates (such as phenolic, aldehydic, and quinonic species) and stable carbonate species responsible for the deactivation of other metal oxides. These insights provide a mechanistic framework for the rational design of robust, chlorine-resistant catalysts for the sustainable abatement of persistent organic pollutants.

Some studies have shown that contaminants can be transferred between floors and the soles, and there are few studies on pollutant propagation caused by human walking in real-life situations. This study explored the propagation and diffusion law of ground pollutants from rubber soles to poly vinyl chloride (PVC) floor during indoor walking through employing a fluorescent solution as a simulant. The footprint decay (D) and transfer efficiency (τ) of the fluorescent solution transferred from the sole to the indoor floor during walking were analyzed based on the fluorescent footprint imaging. The effects of namely body weight (50–75 kg), walking frequency (80–120 steps/min), and solution viscosity (oil and water) were also investigated. It was found that the total fluorescence gray value on the ground decreased exponentially as the number of walking steps (i) increased. The relationship between the normalized gray value of the fluorescent solution (D) on each floor panel i was $D_i=a{e}^{bi},\left(2.1\le a\le 3.8,–1.4\le b\le –0.7\right)$, and τ was distributed in the range of 0.51–0.72. All influencing factors had a significant effect on a, and a greater body weight resulted in a smaller a value, while only the body weight had a significant effect on b and τ, and a greater body weight led to larger b and lower τ values.