Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2024122402
Carbamazepine (CBZ), a typical emerging contaminant, poses significant environmental and health risks due to its frequent detection, high toxicity, and resistance to conventional degradation. This study synthesized a composite material (PH-BC3-600) via high-temperature pyrolysis of mining waste pyrite and discarded Polygonatum kingianum dregs biochar. The composite was employed to activate peroxymonosulfate (PMS) for CBZ degradation. Results demonstrated that biochar incorporation provided pyrite with more active sites, achieving 88.19% removal of 2.5 mg·L−1 CBZ within 5 minutes, with excellent resistance to Cl−, NO3−, and humic acid. Quenching experiments confirmed the involvement of ·OH, SO4·−, 1O2, and e− in the degradation process. The biochar increased the content of highly reductive sulfur species (S2−, S2−2, Sn2−) in PH-BC3-600, facilitating the reduction of Fe(III) to Fe(II) and thereby enhancing PMS activation. Additionally, PH-BC3-600 exhibited lower iron leaching compared to traditional pyrite-based materials, overcoming a key drawback of conventional catalysts. This study highlights the promising potential of PH-BC3-600 for activating PMS in the treatment of emerging contaminants in water.
Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2024112106
Selective synergistic catalytic elimination (SSCE) of CH3SH and CO2 represents a significant approach towards achieving green chemistry objectives. In this study, a series of Al2O3 catalysts with different surface hydroxyl coordination states were designed and fabricated through a simple water bath strategy. The performance of the corresponding catalysts for selective synergistic catalytic elimination of CH3SH and CO2 was systematically evaluated. The catalysts were comprehensively characterized by BET, XRD, XPS, NMR and CO-DRIFTS techniques. The experimental results revealed that the synthesized samples exhibited uniform specific surface areas (150 m2·g−1) and pore sizes (12 nm), while demonstrating varying hydroxyl coordination states, which significantly affects the surface acidity of W-Al2O3 catalyst. Notably, W80-Al2O3, synthesized at 80 °C via water bath heating, displayed the highest proportion of μ1-type hydroxyl coordination. This unique structural feature endowed the catalyst with enhanced Brønsted acidity and superior CO adsorption capacity compared to other catalysts, which significantly promotes the further hydrogenation of CO to CH4 in the SSCE process. As a result, the SSCE performance of W80-Al2O3 was significantly improved, achieving complete conversion of CH3SH (100%) and a CH4 product concentration of 1326 μmol·g−1, which is significantly higher than that of Al2O3 (56 μmol·g−1) and W-Al2O3 (54 μmol·g−1). This work provides a new strategy for the synergistic reduction of typical sulfur-containing odorous pollutants and carbon dioxide.
Journal of Environmental Engineering Technology•2026•DOI: 10.13205/j.hjgc.202604027
Magnesia production processes generate carbon monoxide (CO) emissions, yet publicly available measured data on CO emission factors for these processes remain scarce, constraining the accuracy of emission accounting and mitigation assessment in the industry. To address this data gap, this study selected three representative magnesia-producing enterprises in Anshan, Liaoning Province, China, covering three typical technological routes: the two-stage calcination process (light burning-briquetting-shaft kiln dead burning), the suspension calcination-dead burning sintering process, and the electric arc furnace melting process. Under the condition that enterprises were not equipped with online CO monitoring modules, an estimation approach coupling manual measurements with conventional indicators from the Continuous Emission Monitoring System (CEMS) was developed. By establishing characteristic concentration ratios between CO and nitrogen oxides (NOx) or particulate matter (PM), and combining them with annual CEMS monitoring data, product-level CO emission factors were calculated. The results showed that the CO emission factors for the two-stage calcination process, the suspension calcination–dead burning sintering process, and the electric arc furnace melting process were 5.35, 5.18, and 1.40 kg/t, respectively, among which the emission level of the electric arc furnace melting process was significantly lower than that of sintering-based processes. This study provides enterprise-level measured CO parameters for the magnesia industry, filling the data gap in emission factors for typical technological routes. It also proposes an emission factor estimation method applicable under conditions where online CO monitoring data are unavailable, which can provide methodological support for pollutant emission accounting and emission inventory development in similar data-constrained industries.
Chinese Journal of Environmental Engineering•2026•DOI: 10.12030/j.cjee.202510044
The efficient treatment of sulfur-containing volatile organic compounds (S-VOCs) has become a critical task for air pollution control and green low-carbon transition under China's 14th Five-Year Plan. Industrial emissions often contain multiple S-VOC species, whose interactions can complicate degradation pathways, generate uncontrollable byproducts, and deactivate catalysts, limiting practical application. This review systematically summarizes the past decade of research on catalytic degradation of thiols and thioethers in multi-pollutant systems, focusing on competitive adsorption mechanisms, interfacial reaction pathways, and environmental factor regulation. Performance differences and reaction mechanisms across various catalyst systems under coexisting S-VOCs and inorganic sulfur are compared. Key findings indicate that mixed thiol systems exhibit faster deactivation than single-component systems due to temperature-dependent competitive adsorption and pathway switching, governed by molecular size–active site matching. Strategies such as metal–support strong interactions, zeolite confinement, nanocluster effects, and single-atom catalysts have improved activity and stability. However, dynamic competition mechanisms at active sites remain unresolved. Future research should develop atomic/molecular-level characterization techniques and multi-variable kinetic models, and shift from end-of-pipe purification to resource recovery, e.g., converting H2S and thiols into high-value chemicals like methanethiol, achieving dual goals of pollution control and sulfur resource recycling.
Journal of Environmental Engineering Technology•2026•DOI: 10.13205/j.hjgc.202608017
Carbon monoxide (CO) is a significant gaseous pollutant emitted during high-carbon ferrochrome (HCFeCr) production, yet measured emission factors for different furnace types remain scarce, hindering accurate emission inventories and pollution control assessments. This study addresses this gap by investigating four typical HCFeCr production facilities in Ulanqab, Inner Mongolia, China, comprising two semi-closed submerged arc furnaces (SAFs) and two closed SAFs. A hybrid methodology combining manual stack sampling and continuous emission monitoring system (CEMS) data was employed. A characteristic CO-to-NOx concentration ratio was established from manual measurements, which was then applied to continuous NOx data to estimate CO emissions and product-based emission factors. Results revealed substantial process-dependent variability: semi-closed SAFs (Facilities A and B) exhibited CO emission factors of 7.06 kg/t and 3.66 kg/t, respectively, whereas closed SAFs (Facilities C and D) with associated pelletizing processes showed notably lower factors of 1.41 kg/t and 0.51 kg/t. On average, semi-closed furnaces emitted approximately six times more CO per tonne of product than closed furnaces. Furnace sealing degree and raw material ratios were identified as key determinants. These findings underscore the inadequacy of using a single average emission factor for HCFeCr production and advocate for furnace-type-specific factors to improve emission accounting accuracy. This study provides essential measured data for developing refined CO emission inventories and supporting pollution reduction policies in the ferroalloy industry.