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Emissions from industrial parks are crucial sources of ambient volatile organic compound (VOC) pollution, characterized by high concentrations, complex compositions, dispersed emission sources, and uneven spatial distribution. To better understand and address this issue, it is crucial to analyze the spatial differences in VOC pollution and associated health risks through multi-point monitoring. In this study, we established four online monitoring sites in a typical industrial park in Kaifeng, China. We monitored 115 VOC species and found significant differences in the concentration and chemical composition of total VOCs (TVOCs) among the four sites. Two sites were primarily composed of halohydrocarbons (49.80% and 41.21%), while the other two sites had a higher proportion of aromatics (54.78% and 39.03%). Acetaldehyde was the main contributor to ozone formation potential (OFP) at one site, while toluene was associated with the other three sites. The site with the highest VOC concentration and OFP also showed the highest secondary organic aerosol formation potential (SOAP). In terms of health risk assessment, acrolein posed a non-carcinogenic risk at all sites, but there were disparities in the carcinogenic risk among the four sites. 1,2-Dichloroethane at one site exceeded the definite risk limit, while 1,2-dibromoethane and chloroform were considered probable risk species at another site. Considering both the environmental impact and health risk, we used entropy-weighting to calculate a comprehensive control index (CCI). This index identified 1,2-dichloroethane as the Level Ⅰ controlled pollutant species at two sites, and toluene at the other two sites. This study highlights the spatial heterogeneity in VOC pollution and health risks within the industrial park, providing valuable insights for targeted pollution control strategies. [Display omitted] • Four online monitoring sites for VOCs were established in a typical industrial park. • Obvious spatial differences were found in VOC pollution features and health risks. • Spatial characteristics of priority-controlled species were identified based on CCI. [ABSTRACT FROM AUTHOR]

To understand the characteristics, source apportionment, and regional transport of volatile organic compounds (VOCs) and ozone (O 3) in a typical city with severe air pollution in central China, we observed and analyzed 115 VOC species at an urban site in Zhengzhou from 29 July to 26 September 2021. During this period, observation- and emission-based approaches revealed that Zhengzhou was in a VOC-limited regime. The average concentration of total VOCs (TVOCs) was 162.25 ± 71.42 μg/m3, dominated by oxygenated VOCs (OVOCs, 34.49%), alkanes (24.29%), and aromatics (19.49%). Six VOC sources were identified using positive matrix factorization (PMF) model, including paint solvent usage (25.32%), secondary production (24.11%), industrial production (19.22%), vehicle exhaust (16.18%), biogenic emission (8.87%), and combustion (6.30%). To assess the regional contribution and source apportionment of VOCs and O 3 , Comprehensive Air Quality Model with Extensions (CAMx) with the Ozone Source Apportionment Technology (OSAT) was used for simulation. Results showed that the VOCs were significantly affected by local emissions (about 70%), while O 3 was mainly attributed to regional and super-regional transport. Regarding multi-directional regional transport of VOCs and O 3 , dominant contributions were from the northeast and east-northeast directions, and O 3 contributions were also predominantly from the east and east-southeast directions. In terms of source apportionment, the transportation and industrial sectors (including solvent usage) were the major contributors to O 3 and VOCs. To alleviate VOCs and O 3 pollution, transportation and industrial emission reduction should be strengthened, and regional coordination, especially from the northeast to east-southeast directions, should be emphasized in addition to local management. [Display omitted] • 115 VOC species, including 21 OVOCs, were measured and analyzed in Zhengzhou. • Local emissions mainly affected VOCs (∼70%) rather than O 3. • Regional contributions of VOCs and O 3 were mainly from the NE and ENE directions. • Transportation and industrial sectors were the major contributors to VOCs and O 3. [ABSTRACT FROM AUTHOR]

Few related studies have been carried out for northwest China's the inland, although the increasing inorganic reactive nitrogen (Nr) deposition and severe air pollution in China have attracted considerable attention. Based on eight-year measurements of the concentrations of NH 3 , HNO 3 , particulate (p) NH 4 +, pNO 3 −, and NO 2 in the air and inorganic nitrogen (NH 4 +, NO 3 −) in the precipitation at a rural site in Wuwei, Gansu Province, we quantified the dry and bulk/wet Nr deposition fluxes and analyzed their temporal trends in combination with air pollution data (2015–2018). The concentrations of the single Nr species in the air did not exhibit significant seasonal variations, except for that of pNO 3 − which were the highest in summer and the lowest in winter. The average annual total Nr (dry + bulk) deposition was 27.2 ± 6.7 kg N ha−1 with a significant (p <.05) annual increase rate of 10%, which was dominated by the dry deposition flux (20.8 ± 7.1 kg N ha−1 yr−1) during the entire period. The NH 4 +-N and NO 3 −-N deposition fluxes in the precipitation were significantly (p <.05) higher in the summer than in the other three seasons owing to the heavy rainfall. The reduced N (NH 3 , pNH 4 +, and NH 4 +) deposition flux was 4.7 times that of the oxidized N (HNO 3 , pNO 3 −, NO 2 , and NO 3 −), which increased with a high annual rate (25%). The annual mean concentrations of the main air pollutants (PM 2.5 , PM 10 , SO 2 , NO 2 , and CO) significantly decreased by 15%–76%; in contrast, increasing trends of the O 3 and NH 3 concentrations were observed. Our results highlight the importance of the control of NH 3 emissions and O 3 pollution to comprehensively mitigate N deposition and improve air quality in the considered region. • The total nitrogen deposition increased at an annual rate of 10% from 2010 to 2018. • Nitrogen deposition has become an important nitrogen source to the agroecosystem. • Air pollutants significantly decreased by 15%–76%, except for O 3 and NH 3. • NH 3 concentrations increased at an annual rate of 25% from 2010 to 2018. • Control of NH 3 emission and O 3 pollution is imperative to improve air quality. [ABSTRACT FROM AUTHOR]

• Atmospheric N deposition in China was evaluated by two time-scale deposition databases. • Bulk and dry N deposition reached a peak between 2000 and 2010 and then began a steady decline. • Significant decrease of oxidized N deposition proved the effectiveness of NO x emissions control. • Increase of NH 3 dry deposition highlighted the importance of regional NH 3 mitigation. China has experienced a dramatic change in atmospheric reactive nitrogen (Nr) emissions over the past four decades. However, it remains unclear how nitrogen (N) deposition has responded to increases and/or decreases in Nr emissions. This study quantitatively assesses temporal and spatial variations in measurements of bulk and calculated dry N deposition in China from 1980 to 2018. A long-term database (1980–2018) shows that bulk N deposition peaked in around 2000, and had declined by 45% by 2016–2018. Recent bulk and dry N deposition (based on monitoring from 2011 to 2018) decreased from 2011 to 2018, with current average values of 19.4 ± 0.8 and 20.6 ± 0.4 kg N ha−1 yr−1, respectively. Oxidized N deposition, especially dry deposition, decreased after 2010 due to NO x emission controls. In contrast, reduced N deposition was approximately constant, with reductions in bulk NH 4 +-N deposition offset by a continuous increase in dry NH 3 deposition. Elevated NH 3 concentrations were found at nationwide monitoring sites even at urban sites, suggesting a strong influence of both agricultural and non-agricultural sources. Current emission controls are reducing Nr emissions and deposition but further mitigation measures are needed, especially of NH 3 , built on broader regional emission control strategies. [ABSTRACT FROM AUTHOR]

Precipitation chemistry and atmospheric nitrogen (N) deposition are of great concern worldwide due to their close relationships with air quality and impacts on ecosystems. However, evaluation of the chemical composition of precipitation and N deposition flux in rural areas of Beijing has received little attention to date. This paper presents the chemical constituents, possible sources and wet deposition fluxes of water-soluble ions (NH 4 +, NO 3 −, SO 4 2−, Cl−, Na+, K+, Ca2+, Mg2+) in precipitation samples collected during 2017–2018 at a rural site located at northwest of Beijing city; meanwhile, dry deposition of reactive N species (gaseous ammonia, nitrogen dioxide, nitric acid, and particulate (p) NH 4 + and NO 3 −) were also quantified. During this 2-year period, the volume-weighted mean (VWM) pH of precipitation was 6.73, and all samples had pH values above 6.0. The VWM electric conductivity of precipitation and the mean sum of all measured ions was 43.8 μS cm−1 and 591.9 μeq L−1, respectively, indicating a significant impact of atmospheric pollution. Ca2+ and NH 4 + were the dominant neutralizing species for precipitation acidity. Positive matrix factorization analysis further confirmed five sources for water-soluble ions, including sea salt aging, secondary formation, agriculture, crust, and biomass burning. The annual mean wet N deposition was 4.6, 3.4 and 8.0 kg N ha−1 yr−1 for NH 4 +, NO 3 − and total inorganic N, respectively. The total dry N deposition was dominated by gaseous ammonia (11.5 kg N ha−1 yr−1). The total N deposition (wet plus dry) was 27.7 kg N ha−1 yr−1, where dry deposition contributed to 75% and wet deposition 25% of the total. The simulations from the GEOS-Chem model indicate that agricultural (fertilizer use and livestock) and nonagricultural sources (industry, power plant, and transportation) are both important contributors to total N deposition. These results could be useful in evaluating/developing emission control policies to protect the eco-environment in Beijing. • Precipitation chemistry and nitrogen (N) deposition were investigated in Beijing. • The pH values of precipitation samples were all above 6.0 and averaged 6.7. • Ion source was sea salt, secondary source, agriculture, crust, and biomass burning. • Total N deposition was 27.7 kg N ha−1 yr−1, of which 75% was from dry deposition. • Agricultural and nonagricultural sources contributed equally to total N deposition. [ABSTRACT FROM AUTHOR]