[Characteristics, Sources, and Contributions to Ozone Formation of Ambient Volatile Organic Compounds in Huanggang, China].

Based on the offline sampling data of volatile organic compounds (VOCs) and the simultaneous online measurements of conventional gaseous air pollutants and meteorological parameters in urban Huanggang, the volume fractions and component characteristics of VOCs were analyzed. The sources and ozone (O3) formation sensitivity of VOCs during severe ozone pollution episodes were analyzed using the positive matrix factorization (PMF) model and the photochemical box model coupled with master chemical mechanism (PBM-MCM), respectively. The results revealed that the average volume fractions of total volatile organic compounds were (21.57±3.13)×10-9, with higher volume fractions in winter and spring compared to those in summer and autumn. Among these, alkanes (49.9%) and alkenes (16.4%) accounted for the highest proportion. The PMF analysis results showed that fuel combustion (27.8%), vehicle emission (19.9%), solvent use (15.7%), industrial halogenated hydrocarbon emission (12.1%), chemical enterprise emission (10.5%), natural sources (7.8%), and diesel vehicle emission (6.2%) were the main sources of VOC emissions. Anthropogenic VOCs emitted by solvent use, fuel combustion, and chemical enterprises contributed significantly (60.9% in total) to generating O3, which indicates that these three types of anthropogenic sources should be controlled first when it comes to preventing and controlling ozone pollution. Further, the relative incremental reactivity (RIR) and empirical kinetic method approach (EKMA) revealed that O3 formation was in a VOCs-limited regime during the observation period in Huanggang, China. Furthermore, O3 formation was more sensitive to m-xylene, p-xylene, ethylene, 1-butene, and toluene; therefore, reducing these VOCs should be prioritized.

[Pollution Characteristics and Source Analysis of Carbon and Nitrogen Components in Ambient PM2.5 in Huangshi City].

Based on stable isotope technology and a PMF model, the pollution characteristics and sources of carbon and nitrogen components in ambient PM2.5 in Huangshi City were explored. The results showed that the total carbon concentration[ρ(TC)] and the total carbon isotopic composition (δ13CTC) in ambient PM2.5 in Huangshi City both showed seasonal variation characteristics of being high in winter and low in summer, with values of (4.4±1.2) µg·m-3 and (-26.3±0.5)‰ in summer and (9.9±3.5) µg·m-3 and (-25.5±0.5)‰ in winter, respectively. The total nitrogen concentration[ρ(TN)]was significantly lower in summer[(9.1±9.1) µg·m-3]than that in winter[(62.4±26.4) µg·m-3], whereas the total nitrogen isotopic composition (δ15NTN) was obviously enriched in summer[(12.8±1.9)‰]compared with that in winter[(2.9±4.0)‰]. In addition to the contribution from local sources, the carbon and nitrogen components were mainly affected by the short-range regional emission in northern Hunan and the long-distance transport in the northwest. The MixSIAR model and the PMF model indicated that the vehicle emission source was the main source of carbon components in PM2.5, with contribution rates of 38.9% and 39.3%, respectively. MixSIAR results showed that NOx emission sources had a greater impact on nitrogen components in PM2.5 of different seasons than NH3 emission sources, and their contribution was higher in summer (80%) than that in winter (66.8%), among which the NOx emissions from coal combustion (summer:36.1%; winter:20.2%) had the largest contribution. By contrast, the PMF model indicated that the main source of nitrogen components was vehicle emissions (59.8%). Combining multiple models to overcome the uncertainty and subjectivity of single-model analysis can provide a theoretical basis for actively controlling and reducing fine particulate matter emissions and effectively dealing with urban aerosol pollution.

[Effect of WESP on Emission Characteristics of Condensable Particulate Matter from Ultra-low Emission Coal-fired Power Plants].

In order to study the effect of wet electrostatic precipitators(WESP) on emission characteristics of condensable particulate matter (CPM) from ultra-low emission coal-fired power plants that are under different capacity conditions, a set of CPM sampling devices was built based on US EPA Method 202, and an ultra-low emission coal-fired power plant was detected. This study evaluated the emission level of the CPM from the flue gas of coal-fired power plants, the effects of different unit capacity conditions on the CPM emission concentrations, and the removal efficiency of WESP for different components of the CPM. The results suggested that the emission concentrations of the CPM from ultra-low emission power plants were 27.27 mg·m-3 and 28.71 mg·m-3under the conditions of 75% and 100% capacity, respectively. The removal efficiencies of WESP for the CPM were 35.59% and 27.59%, respectively. SO42- was the main component of water-soluble ions of the CPM. The proportion of SO42- in inorganic components of the CPM reached more than 65% under different capacity conditions. In addition, the removal efficiency of WESP for Cl-, K+, Ca2+, Mg2+, Na+, and other inorganic ions reached 30%-50%, but the mass concentrations of SO42- and NO3- increased.

[Source Analysis of Ambient PM2.5 in Wuhan City Based on Random Forest Model].

Based on the online monitoring data of fine particle(PM2.5) mass concentration, carbonaceous components, ionic constituents, and elemental components in an urban site of Wuhan from December 2019 to November 2020, the chemical characteristics of PM2.5 were analyzed. In addition, seasonal source apportionment of PM2.5 was conducted using the principal component analysis(PCA) method and random forest(RF) algorithm model. The results indicated that ρ(PM2.5) was the highest in winter[(61.33±35.32) µg·m-3] and the lowest in summer[(17.87±10.06) µg·m-3]. Furthermore, organic carbon(OC), with a concentration of(7.27±3.51) µg·m-3, accounted for the major proportion compared with that of elemental carbon(EC) in the carbonaceous component of PM2.5. NO3-, SO42-, and NH4+ had the highest proportion in ionic components, with concentrations of (11.55±3.86),(7.55±1.53), and (7.34±1.99) µg·m-3, respectively. K, Fe, and Ca were the main elements in elemental components, with concentrations of (752.80±183.98),(542.34±142.55), and (459.70±141.99) ng·m-3, respectively. Relying on main factor extraction by PCA and quantitative analysis by RF, five emission sources were ultimately confirmed. The seasonal concentration distribution of these emission sources was as follows:coal burning and secondary sources(46%, 39%, 41%, and 52% for spring, summer, autumn, and winter, respectively) made the highest contribution to PM2.5, followed by vehicle emission sources(22%, 28%, 27%, and 21%), industrial emission sources (14%, 18%, 17%, and 13%), dust sources (10%, 8%, 6%, and 6%), and biomass burning sources (8%, 7%, 9%, and 8%). The valuation of the RF model was evaluated using multiple indicators, including RMSE, MSE, and R2. The evaluation results showed that the model for winter had the best performance (R2=0.974, RMSE=3.795 µg·m-3, MAE=2.801 µg·m-3), the models for spring (R2=0.936, RMSE=3.512 µg·m-3, MAE=2.503 µg·m-3) and autumn (R2=0.937, RMSE=4.114 µg·m-3, MAE=3.034 µg·m-3) performed with moderate-fitting goodness, and the summer model showed a relatively weak-fitting performance (R2=0.866, RMSE=5.665 µg·m-3, MAE=3.889 µg·m-3). The RF model had a satisfactory performance in PM2.5 source apportionment and had excellent prospects in analyzing massive historical data of air pollutants.

[Characteristics of Volatile Organic Compounds in Wood Coatings and Automotive Coatings in China].

Presently, there are a few studies on the measurement of industrial organic solvents in China. To determine the content and species of volatile organic compounds (VOCs) in industrial organic solvents and to provide the emission factors of organic solvents, the Chinese wood and automotive coatings, which accounted for the largest proportion of production in the world, were investigated. Coating samples were obtained by sampling from companies and buying from markets, and were measured in accordance with the domestic standard testing methods for coatings. The content and composition spectrum of VOCs in the coatings were determined, and the ozone formation potential (OFP) was then calculated. The results showed that for wood coatings, the average content of the VOCs in solvent-based, water-based, and ultra-violet (UV) coatings were 37.28%, 9.88%, and 18.02%, respectively. For automotive coatings, the average content of the VOCs in water-based original equipment manufacturer (OEM) coating, solvent-based OEM coating, water-based refinishing coating, and solvent-based refinishing coating were 15.06%, 59.90%, 11.79%, and 54.50%, respectively. The content of the VOCs in different types of coatings varied substantially. The main components and OFP contributors were alcohols and ethers for water-based coatings, benzene series and esters for solvent-based coatings, and esters, alcohols, and ethers for UV coatings. The average value of the coating samples could meet the current mandatory national standards, but 12% of the solvent-based wood coating samples and 42% of the solvent-based OEM coating samples did not meet the standards. In addition, except for the benzene series of the water-based wood coatings, the contents of harmful substances in other coating samples were up to the standards.

Seasonal variations and chemical characteristics of PM(2.5) in Wuhan, central China.

PM2.5 samples were collected at an urban site (WD) and a suburban site (TH) in Wuhan from August 2012 to July 2013. The mass concentrations of water-soluble inorganic ions, carbonaceous species and elements of PM2.5 were measured. The annual mean concentrations of PM2.5 were 106.5 µg/m(3) and 114.9 µg/m(3) at WD and TH, respectively. The chemical compositions of PM2.5 at WD were similar to those at TH and the fractions of the major components of PM2.5 in Wuhan were in the following order of trace elements

Polycyclic aromatic hydrocarbons (PAHs) in the air of Chinese cities.

Polycyclic aromatic hydrocarbons (PAHs) were determined in the air of 37 cities and 3 rural locations across China during the winter, spring, summer and autumn of 2005, using polyurethane foam (PUF) disks as passive air samplers (PAS). Winter and autumn concentrations in cities exceeded spring and summer values. Concentrations were amongst the highest in the world; seasonally averaged autumn/winter values in some cities in the north and north-west of China exceeded proposed European Union air quality standards. Several factors, acting in combination, influenced air concentrations. A significant negative correlation was found between average annual city concentrations and the annual average temperature, while winter time PAH concentrations correlated with estimated coal consumption. The highest total PAH concentrations and loadings of high molecular weight compounds generally occurred in major cities located on higher land (500-2000 m), where relatively cold winters and higher coal consumption occurs. Lower values occurred in cities located in the south and east China and along the coastal regions. Molecular markers indicated incomplete combustion of fossil fuels dominated the urban air and gave evidence for photo-decomposition of selected compounds.

Cloning, sequencing and characterization of the alpha-aminoadipate reductase gene (LYS2) from Saccharomycopsis fibuligera.

The gene putatively encoding alpha-aminoadipate reductase (AAR) was isolated successfully by degenerate PCR and chromosome walking, based on cassette PCR methods, from the dimorphous yeast Saccharomycopsis fibuligera PD70 and was named SfLYS2. Sequence analysis revealed that it contained a putative open reading frame (ORF) of 4161 bp and encoded a polypeptide of 1386 amino acids. The deduced translation product shared an identity of 53% and 51% to the Lys2p homologues of Candida albicans and Saccharomyces cerevisiae, respectively. An atypical TATA box and a GCN4-box element were found in the 5'-upstream region. Genomic Southern hybridization suggested the presence of a single locus of SfLYS2 in the S. fibuligera genome. Expression of the ORF of SfLYS2 in a lys2(-) strain of S. cerevisiae could functionally complement the lysine mutant of the S. cerevisiae strain. S. fibuligera could use lysine as the sole nitrogen source but its growth was inhibited on the alpha-aminoadipate (AA) medium. Approximately 90% of the mutants of S. cerevisiae resistant to AA are lysine auxotrophs; in contrast all the mutants of S. fibuligera resistant to AA recovered in this work were not lysine auxotrophs.

Extremely rapid extraction of DNA from bacteria and yeasts.

A very simple and rapid method for extracting genomic DNA from Gram-negative bacteria, Gram-positive bacteria and yeasts is presented. In this method, bacteria or yeasts are lysed directly by phenol and the supernatant is extracted with chloroform to remove traces of phenol. The supernatant contains DNA that is suitable for molecular analyses, such as PCR, restriction enzyme digestion and genomic library construction. This method is reproducible and simple for the routine DNA extraction from bacteria and yeasts.