Xinlei Ge

Regional Influence of Aerosol Emissions from Wildfires Driven by Combustion Efficiency: Insights from the BBOP Campaign

Wildfires are important contributors to atmospheric aerosols and a large source of emissions that impact regional air quality and global climate. In this study, the regional and nearfield influences of wildfire emissions on ambient aerosol concentration and chemical properties in the Pacific Northwest region of the United States were studied using real-time measurements from a fixed ground site located in Central Oregon at the Mt. Bachelor Observatory (∼2700 m a.s.l.) as well as near their sources using an aircraft. The regional characteristics of biomass burning aerosols were found to depend strongly on the modified combustion efficiency (MCE), an index of the combustion processes of a fire. Organic aerosol emissions had negative correlations with MCE, whereas the oxidation state of organic aerosol increased with MCE and plume aging. The relationships between the aerosol properties and MCE were consistent between fresh emissions (∼1 h old) and emissions sampled after atmospheric transport (6-45 h), suggesting that biomass burning organic aerosol concentration and chemical properties were strongly influenced by combustion processes at the source and conserved to a significant extent during regional transport. These results suggest that MCE can be a useful metric for describing aerosol properties of wildfire emissions and their impacts on regional air quality and global climate.

Waste-to-energy: Dehalogenation of plastic-containing wastes

The dehalogenation measurements could be carried out with the decomposition of plastic wastes simultaneously or successively. This paper reviewed the progresses in dehalogenation followed by thermochemical conversion of plastic-containing wastes for clean energy production. The pre-treatment method of MCT or HTT can eliminate the halogen in plastic wastes. The additives such as alkali-based metal oxides (e.g., CaO, NaOH), iron powders and minerals (e.g., quartz) can work as reaction mediums and accelerators with the objective of enhancing the mechanochemical reaction. The dehalogenation of waste plastics could be achieved by co-grinding with sustainable additives such as bio-wastes (e.g., rice husk), recyclable minerals (e.g., red mud) via MCT for solid fuels production. Interestingly, the solid fuel properties (e.g., particle size) could be significantly improved by HTT in addition with lignocellulosic biomass. Furthermore, the halogenated compounds in downstream thermal process could be eliminated by using catalysts and adsorbents. Most dehalogenation of plastic wastes primarily focuses on the transformation of organic halogen into inorganic halogen in terms of halogen hydrides or salts. The integrated process of MCT or HTT with the catalytic thermal decomposition is a promising way for clean energy production. The low-cost additives (e.g., red mud) used in the pre-treatment by MCT or HTT lead to a considerable synergistic effects including catalytic effect contributing to the follow-up thermal decomposition.

Aerosol characteristics and sources in Yangzhou, China resolved by offline aerosol mass spectrometry and other techniques

Detailed chemical characterization of fine aerosols (PM2.5) is important for reducing air pollution in densely populated areas, such as the Yangtze River Delta region in China. This study systematically analyzed PM2.5 samples collected during November 2015 to April 2016 in urban Yangzhou using a suite of techniques, in particular, an Aerodyne soot particle aerosol mass spectrometry (SP-AMS). The techniques used here reconstructed the majority of total PM2.5 measured where extracted species comprised on average 91.2%. Source analyses of inorganic components showed that secondary nitrate, sulfate and chloride were the major species, while primary sources including biomass burning, coal combustion, traffic, industry and re-suspended dust due to nearby demolition activities, could contribute to other species. EC-tracer method estimated that the organic matter (OM) was composed of 65.4% secondary OM (SOM) and 34.6% primary OM (POM), while the SP-AMS analyses showed that the OM was comprised of 60.3% water-soluble OM (WSOM) and 39.7% water-insoluble OM (WIOM). Correlation analyses suggested that WSOM might be rich in secondary organic species, while WIOM was likely mainly comprised of primary organic species. We further conducted positive matrix factorization (PMF) analyses on the WSOM, and identified three primary factors including traffic, cooking and biomass burning, and two secondary factors. We found the secondary factors dominated WSOM mass (68.1%), and their mass contributions increased with the increase of WSOM concentrations. Relatively small contribution of primary sources to WSOM was probably due to their low water solubility, which should be investigated further in future. Overall, our findings improve understanding of the complex aerosol sources and chemistry in this region.

Pyrite transformation and sulfur dioxide release during calcination of coal gangue

Calcination is a typical process associated with the utilization of coal gangue. A concern associated with this procedure is the emission of sulfur dioxide (SO2). In this work, the behavior of SO2 release during coal gangue calcination under an air atmosphere were systematically investigated and compared to the characteristics of SO2 evolution from pure pyrite calcination. Results show that although sulfur in coal gangue mainly exists in the form of pyrite, it represents different transformation behaviors from that in pure mineral pyrite. At 500 °C, the release rate of SO2 is significantly higher in coal gangue than in mineral pyrite due to the fact that coal gangue combustion can occur at low temperatures, which favors the SO2 release, while at 600 and 700 °C they become almost the same. The shrinking core model cannot describe the SO2 emission profiles in coal gangue and, instead, a hybrid 3D diffusion, i.e. the Jander model, is successfully developed in this study.

Catalytic oxidation of nitric oxide (NO) with carbonaceous materials

The catalytic oxidation of NO to NO2 at ambient temperatures has been a promising route for controlling NO emissions, since NO2 is subsequently removed as nitric acid in the presence of water. Because of their large surface area, high porosity, and relative chemical inertness, carbon-based materials are very attractive in de-nitrification (De-NOx) as catalysts or catalyst supports. This paper reviewed the catalytic oxidation of NO to NO2 over commonly-used carbon materials including activated carbons (ACs), activated carbon fibers (ACFs) and carbon xerogels (CXs). The NO conversion is often influenced by the surface characteristics of carbon materials (e.g., pore structure, surface areas, functional groups, and morphology), O2 concentration, and reaction temperature. With the addition of metal actives, the catalytic performance could be significantly improved. Catalytic reaction and adsorption are two key points. Further, the strong dependence of NO conversion on the O2 concentration concludes that O2 is first adsorbed on the carbon surface, and then it reacts with NO to form adsorbed NO2, which desorbs to the gas phase. Considering the economic efficiency, carbon precursors from biomasses could be fabricated into the desired carbonaceous materials by means of functionalization. In addition, the integrated strategy of desulfurization (De-SOx) and De-NOx could be developed by carbon materials with the proper modification methods.

Quantitative Relationship between Cadmium Uptake and the Kinetics of Phytochelatin Induction by Cadmium in a Marine Diatom.

Heavy metals activate the synthesis of phytochelatins (PCs), while the induced PCs might affect metal uptake via chelating intracellular free metals. However, the relationship of PCs to metal uptake is poorly understood. In this study, we examined the kinetics of cadmium (Cd) accumulation and the synthesis of PCs in a marine diatom, Thalassiosira weissflogii, under different irradiance levels. Irradiance alone could not change the concentrations of PCs in the Cd-free treatments, while higher irradiance accelerated the induction of intracellular PCs at the same [Cd2+] level. PC-SH (2 × PC2 + 3 × PC3 + 4 × PC4) was bound with Cd at a stoichiometric ratio of 2 to 49 in our short-term uptake experiments, indicating that PC induction is sufficient to serve as the first line of defense against Cd stress. A positive linear correlation between the induction rate of PCs and the Cd uptake rate was observed, while the ratio of the PC content to intracellular Cd varied greatly when the irradiance was increased several fold. Because metal uptake has been successfully used in predicting acute metal toxicity, our findings are helpful for understanding the role of PCs in metal detoxification and developing PCs as biomarkers for metal sensitivity.

The partitioning behavior of trace element and its distribution in the surrounding soil of a cement plant integrated utilization of hazardous wastes

In the present study, the trace elements partitioning behavior during cement manufacture process were systemically investigated as well as their distribution behaviors in the soil surrounding a cement plant using hazardous waste as raw materials. In addition to the experimental analysis, the thermodynamic equilibrium calculations were simultaneously conducted. The results demonstrate that in the industrial-scale cement manufacture process, the trace elements can be classified into three groups according to their releasing behaviors. Hg is recognized as a highly volatile element, which almost totally partitions into the vapor phase. Co, Cu, Mn, V, and Cr are considered to be non-volatile elements, which are largely incorporated into the clinker. Meanwhile, Cd, Ba, As, Ni, Pb, and Zn can be classified into semi-volatile elements, as they are trapped into clinker to various degrees. Furthermore, the trace elements emitted into the flue gas can be adsorbed onto the fine particles, transport and deposit in the soil, and it is clarified here that the soil around the cement plant is moderately polluted by Cd, slightly polluted by As, Cr, Ba, Zn, yet rarely influenced by Co, Mn, Ni, Cu, Hg, and V elements. It was also estimated that the addition of wastes can efficiently reduce the consumption of raw materials and energy. The deciphered results can thus provide important insights for estimating the environmental impacts of the cement plant on its surroundings by utilizing wastes as raw materials.

Micro-mesoporous carbons from original and pelletized rice husk via one-step catalytic pyrolysis

This paper studied the KOH-catalyzed pyrolysis of rice husk (RH) and its pellet (RHP) at a high temperature (750 °C) for activated bio-carbons production. The mass ratio of KOH and biomass greatly impacted the pyrolysis kinetic and biochar property. The KOH catalysis (mass ratio: 1) reduced significantly the activation energy to 41 kJ/mol. During carbonization with KOH, the in-situ generated K2CO3 tailored the morphology and size of the self-template (SiO2 nanoparticles), giving rise to the chars with the open foam-like porous architectures enrich in micro- and meso-pores. Thus, the KOH activation via one-step pyrolysis could produce the micro-mesoporous carbons (e.g., RH-char 1 and RHP-char 1) with high specific surface areas and high content of oxygen-functionalities. Furthermore, the hierarchical porous carbons have high potential applications in adsorption process and electrochemical energy storage (e.g., supercapacitor) because of their unique physicochemical properties.

Characterization of Fine Particulate Matter and Associated Health Burden in Nanjing

Particulate matter (PM) air pollution has become a serious environmental problem in Nanjing and poses great health risks to local residents. In this study, characteristics of particulate matter with an aerodynamic diameter less than 2.5 μm (PM2.5) over Nanjing were analyzed using hourly and daily averaged PM2.5 concentrations and meteorological parameters collected from nine national monitoring sites during the period of March 2014 to February 2017. Then, the integrated exposure-response (IER) model was applied to assess premature mortality, years of life lost (YLL) attributable to PM2.5, and mortality benefits due to PM2.5 reductions. The concentrations of PM2.5 varied among hours, seasons and years, which can be explained by differences in emission sources, secondary formations and meteorological conditions. The decreased ratio of PM2.5 to CO suggested that secondary contributions decreased while the relative contributions of vehicle exhaust increased from increased CO data. According to the values of attributable fractions (AF), stroke was the major cause of death, followed by ischemic heart disease (IHD), lung cancer (LC) and chronic obstructive pulmonary disease (COPD). The estimated total deaths in Nanjing due to PM2.5 were 12,055 and 10,771, leading to 98,802 and 87,647 years of life lost in 2014 and 2015, respectively. The elderly and males had higher health risks than youngsters and females. When the PM2.5 concentrations meet the World Health Organization (WHO) Air Quality Guidelines (AQG) of 10 μg/m3, 84% of the premature deaths would be avoided, indicating that the Nanjing government needs to adopt more stringent measure to reduce PM pollution and enhance the health benefits.

Aqueous-Phase Secondary Organic Aerosol Formation Via Reactions with Organic Triplet Excited States—a Short Review

Secondarily formed species are found to play significant and often dominant roles in the particular matter pollution. However, the formation mechanisms of secondary organic species are highly complex thus are much less understood. This short review summarizes current studies regarding the secondary organic aerosol formed in atmospheric aqueous phases (cloud/fog drops and aqueous aerosols) via oxidation by the organic triplet excited states, including the current systems of interests, and major findings, etc. Overall, this specific formation route is relatively less studied but likely important in atmospheric chemistry. Future research needs and directions of this reaction pathway are proposed. Particularly, more studies are needed to elucidate its role in atmospheric processes regarding humic-like substances, detailed chemical characterization of the reaction products and efforts to account for influences of such pathway into air quality models.