中国钢铁行业CO2减排技术及成本研究

钢铁行业是我国主要的能源消费及CO₂排放行业,推动钢铁行业低碳绿色发展已成为实现我国碳达峰、碳中和的重要环节。为此,研究围绕能源结构调整、工艺结构优化、节能减排技术推广和CCUS技术应用4方面,通过设置基础情景、稳定发展情景和强化减排情景3类情景,利用边际减排成本曲线对我国钢铁行业34项减排技术的减排成本和减排潜力进行分析。结果表明:在稳定发展情景下,我国钢铁行业平均减排成本为433元/tCO₂,所有技术的总减排成本为2100亿元,总减排潜力为4.9亿t。在各项减排技术中,废铁-电弧炉炼钢具有较高的减排经济效益,其以较低的单位减排成本贡献了钢铁行业近50%的碳减排量。未来,我国应加快推进长流程炼钢向短流程炼钢的发展,推动钢铁行业生产工艺的结构性调整。     

An unusual high ozone event over the North and Northeast China during the record-breaking summer in 2018

Under the background of global warming, the summer temperature of the North and Northeast China (NNEC) has significantly increased since 2017, which was accompanied by the aggravated ozone (O₃) pollution. In 2018, the NNEC experienced a record-breaking summer of the past 40 years. Influenced by the abnormal high temperatures, a regional ozone event occurred on 2-3 August, over 63% of 79 selected cities in the NNEC were exposed to O₃ pollution, and the maximum value of MDA8 O₃ reached 268 μg/m³. Observations indicated that ozone concentrations agree well with the maximum temperature at 2 meters (MT2M) over NNEC with a correlation coefficient of 0.69. During the pollution episode, strong downdraft in the local high (35°N-42.5°N, 112.5°E-132.5°E; LH) over the NNEC created the favourable meteorological conditions for O₃ formation. By analyzing the horizontal wind and wave activity fluxes (WAFs) at 200 hPa, we found that the LH formation was resulted from the Rossby wave propagation from upstream along the mid-latitude Asian jet. The split polar vortex intrusion further strengthened the amplitude of the Rossby wave and reinforced the LH. Moreover, a secondary circulation between Typhoon Jongdari and the LH contributed to the enhanced LH with strong subsidence. On the other hand, the stratospheric intrusions under the deep subsidence also contributed to the enhanced surface O₃. In this study, the deep-seated meteorological dynamical mechanisms contributing to the abnormal high temperatures were investigated, which can lead to a better understanding of the regional O₃ pollution over NNEC under the global-warming background.     

Removal of antibiotic-resistant genes during drinking water treatment: A review

Once contaminate the drinking water source, antibiotic resistance genes (ARGs) will propagate in drinking water systems and pose a serious risk to human health. Therefore, the drinking water treatment processes (DWTPs) are critical to manage the risks posed by ARGs. This study summarizes the prevalence of ARGs in raw water sources and treated drinking water worldwide. In addition, the removal efficiency of ARGs and related mechanisms by different DWTPs are reviewed. Abiotic and biotic factors that affect ARGs elimination are also discussed. The data on presence of ARGs in drinking water help come to the conclusion that ARGs pollution is prevalent and deserves a high priority. Generally, DWTPs indeed achieve ARGs removal, but some biological treatment processes such as biological activated carbon filtration may promote antibiotic resistance due to the enrichment of ARGs in the biofilm. The finding that disinfection and membrane filtration are superior to other DWTPs adds weight to the advice that DWTPs should adopt multiple disinfection barriers, as well as keep sufficient chlorine residuals to inhibit re-growth of ARGs during subsequent distribution. Mechanistically, DWTPs obtain direct and inderect ARGs reduction through DNA damage and interception of host bacterias of ARGs. Thus, escaping of intracellular ARGs to extracellular environment, induced by DWTPs, should be advoided. This review provides the theoretical support for developping efficient reduction technologies of ARGs. Future study should focus on ARGs controlling in terms of transmissibility or persistence through DWTPs due to their biological related nature and ubiquitous presence of biofilm in the treatment unit.     

Co-metabolic and biochar-promoted biodegradation of mixed PAHs by highly efficient microbial consortium QY1

Polycyclic aromatic hydrocarbons (PAHs), typical representatives of the persistent organic pollutants (POPs), have become ubiquitous in the environment. In this study, a novel microbial consortium QY1 that performed outstanding PAHs-degrading capacity has been enriched. The degradation characteristics of single and mixed PAHs treated with QY1 were studied, and the effect of biochar on biodegradation of mixed PAHs and the potential of biochar in PAHs-heavy metal combined pollution bioremediation were also investigated. Results showed that, in single substrate system, QY1 degraded 94.5% of 500 mg/L phenanthrene (PHE) and 17.8% of 10 mg/L pyrene (PYR) after 7 days, while in PHE-PYR mixture system, the biodegradation efficiencies of PHE (500 mg/L) and PYR (10 mg/L) reached 94.0% and 96.2%, respectively, since PHE served as co-metabolic substrate to have significantly improved PYR biodegradation. Notably, with the cooperation of biochar, the biodegradations of PHE and PYR were greatly accelerated. Further, biochar could reduce the adverse impact of heavy metals (Cd²⁺, Cu²⁺, Cr₂O₇^2?) on PYR biodegradation remarkably. The sequencing analysis revealed that Methylobacterium, Burkholderia and Stenotrophomonas were the dominant genera of QY1 in almost all treatments, indicating that these genera might play key roles in PAHs biodegradation. Overall, this study provided new insights into the efficient bioremediation of PAHs-contaminated site.     

Potential applications of porous organic polymers as adsorbent for the adsorption of volatile organic compounds

Volatile organic compounds (VOCs) with high toxicity and carcinogenicity are emitted from kinds of industries, which endanger human health and the environment. Adsorption is a promising method for the treatment of VOCs due to its low cost and high efficiency. In recent years, activated carbons, zeolites, and mesoporous materials are widely used to remove VOCs because of their high specific surface area and abundant porosity. However, the hydrophilic nature and low desorption rate of those materials limit their commercial application. Furthermore, the adsorption capacities of VOCs still need to be improved. Porous organic polymers (POPs) with extremely high porosity, structural diversity, and hydrophobic have been considered as one of the most promising candidates for VOCs adsorption. This review generalized the superiority of POPs for VOCs adsorption compared to other porous materials and summarized the studies of VOCs adsorption on different types of POPs. Moreover, the mechanism of competitive adsorption between water and VOCs on the POPs was discussed. Finally, a concise outlook for utilizing POPs for VOCs adsorption was discussed, noting areas in which further work is needed to develop the next-generation POPs for practical applications.     

Thermal defluorination behaviors of PFOS,PFOA and PFBS during regeneration of activated carbon by molten salt

• New method of mineralizing PFCs was proposed. • Activated carbon was regenerated while mineralizing PFCs. • Molten NaOH has good mineralization effect on PFOS and PFBS. Current study proposes a green regeneration method of activated carbon (AC) laden with Perfluorochemicals (PFCs) from the perspective of environmental safety and resource regeneration. The defluorination efficiencies of AC adsorbed perfluorooctanesulfonate (PFOS), perfluorooctanoic acid (PFOA) and perfluorobutanesulfonate (PFBS) using three molten sodium salts and one molten alkali were compared. Results showed that defluorination efficiencies of molten NaOH for the three PFCs were higher than the other three molten sodium salts at lower temperature. At 700°C, the defluorination efficiencies of PFOS and PFBS using molten NaOH reached to 84.2% and 79.2%, respectively, while the defluorination efficiency of PFOA was 35.3%. In addition, the temperature of molten salt, the holding time and the ratio of salt to carbon were directly proportional to the defluorination efficiency. The low defluorination efficiency of PFOA was due to the low thermal stability of PFOA, which made it difficult to be captured by molten salt.The weight loss range of PFOA was 75°C–125°C, which was much lower than PFOS and PFBS (400°C–500°C). From the perspective of gas production, fluorine-containing gases produced from molten NaOH-treated AC were significantly reduced, which means that environmental risks were significantly reduced. After molten NaOH treatment, the regenerated AC had higher adsorption capacity than that of pre-treated AC.     

Fabrication and characterization of lightweight aggregate prepared from steel mill sludge in one step

Journal of Material Cycles and Waste Management - The qualified green lightweight aggregate (LWA) was successfully prepared from steel mill sludge (SMS) and fly ash (FAS) in one step using the...     

Calcined Oil Shale Semi-coke for Significantly Improved Performance Alginate-Based Film by Crosslinking with Ca2+

Journal of Polymers and the Environment - Oil shale semi-coke (OSSC) is the residual solid waste after refining of oil shale, which principally contains organic matter and minerals. The common...     

Worldwide cases of water pollution by emerging contaminants: a review

Environmental Chemistry Letters - Water contamination by emerging contaminants is increasing in the context of rising urbanization, industrialization, and agriculture production. Emerging...     

Assessment of popular techniques for co-processing municipal solid waste in Chinese cement kilns

• Municipal solid waste (MSW) was fermented, screened, gasified, then co-processed. • Co-processing MSW in cement kilns could cause excessive pollutant emissions. • Bypass flue gas can be disposed of through the main flue system. • Popular MSW co-processing methods do not affect cement quality. Cement kiln co-processing techniques have been developed in the past 20 years in China, and more than 60 factories now use fermentation, screening, and gasification pre-treatment techniques to co-process municipal solid waste (MSW). There three complete MSW pre-treatment techniques, co-processing procedures, and environmental risk assessments have been described in few publications. In this study, we assessed the effectiveness of each technique. The results suggested that the pollutant content released by each pre-treatment technology was lower than the emission standard. To reveal the mechanisms of pollutant migration and enrichment, the substances in the kiln and kiln products are investigated. The input of co-processing materials (Co-M) produced by fermentation caused formation of polychlorinated dibenzo-p-dioxins and dibenzofuran (PCDD/Fs) in the bypass flue gas (By-gas) in excess of the regulatory standard. The Co-M input produced by the screening and gasifier technologies caused the total organic carbon (TOC) concentration to exceed the standard. In addition, the NO_x, TOC, and PCDD/Fs in the By-gas exceeded the regulatory standard. Raw meal was the primary chlorine and heavy metals input stream, and clinker (CK) and cement kiln dust (CKD) accounted for>90% of the total chlorine output stream. Flue gas and CKD were the primary volatile heavy metal (Hg) output streams. Greater than 70% of the semi-volatile heavy metals (Cd, Pb, Tl and Se) distributed in hot raw meal and bypass cement kiln dust. The low-volatility heavy metals were concentrated in the CK. These results indicated that co-processing techniques used in China still require improvement.