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  • 1
    In: Atmosphere, MDPI AG, Vol. 13, No. 4 ( 2022-04-17), p. 634-
    Abstract: In this study, the characteristics and formation mechanism of summertime isoprene, monoterpene, and toluene-derived secondary organic aerosols (SOAs) were investigated in a rural area of Guanzhong Plain, Northwest China. The variations in key indicators of primary sources indicated a significant influence of biomass burning on PM2.5 during the observation period. The concentrations of total measured SOA tracers from isoprene, monoterpene, and toluene were 40.85 ± 17.31, 24.27 ± 7.50, and 10.61 ± 0.33 ng/m3, respectively. The average ratio of cis-pinonic and pinic acids to 3-Methyl-1,2,3-butanetricarboxylic acid (MBTCA)(P/M) were 0.45 and 0.85 by day and by night, respectively. The low ratio in the daytime was mainly due to the stronger photo-degradation and particle-to-gas distribution of semi-volatile cis-pinonic and pinic acids. The monoterpene SOA tracers were significantly correlated with levoglucosan at night (R2 = 0.51, p 〈 0.01), as were toluene SOA tracers and levoglucosan (R2 〉 0.67, p 〈 0.01), indicating the significant contribution of biomass combustion to these SOAs. The mass concentration of isoprene-, monoterpenes-, and toluene-derived SOC was estimated by using the tracer yield method. The total calculated SOCs by day and by night were 0.25–0.71 (average: 0.46) and 0.26–0.78 (average: 0.42) µgC/m3, accounting for 3.35–10.58% and 3.87–13.51% of OC by day and by night, respectively.
    Type of Medium: Online Resource
    ISSN: 2073-4433
    Language: English
    Publisher: MDPI AG
    Publication Date: 2022
    detail.hit.zdb_id: 2605928-9
    SSG: 23
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  • 2
    In: Atmosphere, MDPI AG, Vol. 6, No. 2 ( 2015-02-05), p. 195-208
    Type of Medium: Online Resource
    ISSN: 2073-4433
    Language: English
    Publisher: MDPI AG
    Publication Date: 2015
    detail.hit.zdb_id: 2605928-9
    SSG: 23
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  • 3
    In: Atmosphere, MDPI AG, Vol. 10, No. 5 ( 2019-05-16), p. 277-
    Abstract: Comparisons of aerosol composition and sources in different cities or regions are rather limited, yet important for an in-depth understanding of the spatial diversity of aerosol pollution in China. In this study, the data originating from 25 different winter aerosol mass spectrometer (AMS)/aerosol chemical speciation monitor (ACSM) studies were used to provide spatial coverage of the Beijing-Tianjin-Hebei (BTH), Guanzhong (GZ), Yangtze River Delta (YRD), and Pearl River Delta (PRD) regions. The spatial distribution and diurnal variations in aerosol composition and organic sources were analyzed to investigate the aerosol characteristics in the four regions. It was found that there were differences in the compositions of non-refractory particulate matter across the regions, e.g., more sulfate in the PRD versus more nitrate in the YRD, as well as in the organic sources, e.g., more coal combustion in BTH versus more biomass burning in GZ. The characteristics of the composition of NR-PM are similar when the campaigns were classified according to the winter of different years or the cities of different regions. The diurnal variation of the PRD-sulfate indicated its regional nature, whereas the organics from burning sources in two regions of northern China exhibited local characteristics. Based on these findings, we suggest that strict control policies for coal combustion and biomass burning emissions should be enforced in the BTH and GZ regions, respectively.
    Type of Medium: Online Resource
    ISSN: 2073-4433
    Language: English
    Publisher: MDPI AG
    Publication Date: 2019
    detail.hit.zdb_id: 2605928-9
    SSG: 23
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  • 4
    In: Atmosphere, MDPI AG, Vol. 13, No. 7 ( 2022-06-30), p. 1042-
    Abstract: Previous studies have determined biomass burning as a major source of air pollutants in the ambient air in Thailand. To analyse the impacts of meteorological parameters on the variation of carbonaceous aerosols and water-soluble ionic species (WSIS), numerous statistical models, including a source apportionment analysis with the assistance of principal component analysis (PCA), hierarchical cluster analysis (HCA), and artificial neural networks (ANNs), were employed in this study. A total of 191 sets of PM2.5 samples were collected from the three monitoring stations in Chiang-Mai, Bangkok, and Phuket from July 2020 to June 2021. Hotspot numbers and other meteorological parameters were obtained using NOAA-20 weather satellites coupled with the Global Land Data Assimilation System. Although PCA revealed that crop residue burning and wildfires are the two main sources of PM2.5, ANNs highlighted the importance of wet deposition as the main depletion mechanism of particulate WSIS and carbonaceous aerosols. Additionally, Mg2+ and Ca2+ were deeply connected with albedo, plausibly owing to their strong hygroscopicity as the CCNs responsible for cloud formation.
    Type of Medium: Online Resource
    ISSN: 2073-4433
    Language: English
    Publisher: MDPI AG
    Publication Date: 2022
    detail.hit.zdb_id: 2605928-9
    SSG: 23
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  • 5
    In: Catalysts, MDPI AG, Vol. 12, No. 5 ( 2022-05-19), p. 560-
    Abstract: Various reaction mechanisms for the catalytic degradation of formaldehyde (HCHO) remain to be debated. Density functional theory (DFT) was applied to investigate whether the catalytic oxidation of HCHO on pristine Co3O4 (110) surface follows the Mars-van Krevelen (MvK) mechanism or the Langmuir–Hinshelwood (L-H) mechanism. Firstly, HCHO and O2 co-adsorb on the surface and two H atoms from HCHO are peculiarly prone to transfer to O2, forming CO and HOOH. For the MvK mechanism, CO2 is generated through CO grabbing a lattice oxygen. Meanwhile, the O–O bond of HOOH is broken into two OH groups. One OH fills the oxygen vacancy and its H atom moves to another OH group for H2O formation. For the L-H mechanism, CO directly obtains one OH group to generate COOH. Subsequently, the H atom of COOH transfers to another OH group along with CO2 and H2O generation. Both two mechanisms exhibit a similar maximum activation barrier. The lattice oxygen in the MvK mechanism and the surface-absorbed OH group in the L-H mechanism are the key reactive oxygen species. The small difference in energetic span further suggests that the catalytic cycle through the two mechanisms is feasible. This theoretical study provides new insight into the catalytic reaction path of HCHO oxidation on pristine Co3O4 surface.
    Type of Medium: Online Resource
    ISSN: 2073-4344
    Language: English
    Publisher: MDPI AG
    Publication Date: 2022
    detail.hit.zdb_id: 2662126-5
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  • 6
    In: Atmosphere, MDPI AG, Vol. 6, No. 3 ( 2015-03-17), p. 361-379
    Abstract: Secondary organic carbon (SOC) formation and its effects on human health require better understanding in Chinese megacities characterized by a severe particulate pollution and robust economic reform. This study investigated organic carbon (OC) and elemental carbon (EC) in PM2.5 and PM0.25 collected 8–20 March 2012. Samples were collected inside and outside a classroom in a middle school at Xi’an. On average, OC and EC accounted for 20%–30% of the particulate matter (PM) mass concentration. By applying the EC-tracer method, SOC’s contribution to OC in both PM size fractions was demonstrated. The observed changes in SOC:OC ratios can be attributed to variations in the primary production processes, the photochemical reactions, the intensity of free radicals, and the meteorological conditions. Total carbon (TC) source apportionment by formula derivation showed that coal combustion, motor vehicle exhaust, and secondary formation were the major sources of carbonaceous aerosol. Coal combustion appeared to be the largest contributor to TC (50%), followed by motor vehicle exhaust (25%) and SOC (18%) in both size fractions.
    Type of Medium: Online Resource
    ISSN: 2073-4433
    Language: English
    Publisher: MDPI AG
    Publication Date: 2015
    detail.hit.zdb_id: 2605928-9
    SSG: 23
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  • 7
    In: Remote Sensing, MDPI AG, Vol. 10, No. 8 ( 2018-07-24), p. 1169-
    Abstract: A thorough understanding of aerosol optical properties and their spatio-temporal variability are required to accurately evaluate aerosol effects in the climate system. In this study, a multi-year study of aerosol optical and microphysical properties was firstly performed in Xi’an based on three years of sun photometer remote sensing measurements from 2012 to 2015. The multi-year average of aerosol optical depth (AOD) at 440 nm was about 0.88 ± 0.24 (mean ± SD), while the averaged Ångström Exponent (AE) between 440 and 870 nm was 1.02 ± 0.15. The mean value of single scattering albedo (SSA) was around 0.89 ± 0.03. Aerosol optical depth and AE showed different seasonal variation patterns. Aerosol optical depth was slightly higher in winter (0.99 ± 0.36) than in other seasons (~0.85 ± 0.20), while AE showed its minimum in spring (0.85 ± 0.05) due to the impact of dust episodes. The seasonal variations of volume particle size distribution, spectral refractive index, SSA, and asymmetry factor were also analyzed to characterize aerosols over this region. Based on the aerosol products derived from sun photometer measurements, the classification of aerosol types was also conducted using two different methods in this region. Results show that the dominant aerosol types are absorbers in all seasons, especially in winter, demonstrating the strong absorptivity of aerosols in Xi’an.
    Type of Medium: Online Resource
    ISSN: 2072-4292
    Language: English
    Publisher: MDPI AG
    Publication Date: 2018
    detail.hit.zdb_id: 2513863-7
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  • 8
    In: Atmosphere, MDPI AG, Vol. 10, No. 11 ( 2019-10-25), p. 645-
    Abstract: The Tibetan Plateau (TP) is one of the world’s most sensitive areas for climate change. Previous studies have revealed that air pollutants emitted from South and Southeast Asia can be transported to and have a negative impact on the TP. However, the majority of the investigators have focused on the pollutant transport processes from South Asian regions (i.e., India and Bangladesh) and parts of Southeast Asia, while the regions adjacent to the southeast fringe of the TP (i.e., Burma and the Sino-Burmese border) have been neglected. Here, fine particulate matter (PM2.5) samples were collected during the period 11 March to 13 May 2018 at Gaomeigu, a high-altitude remote site in the southeastern margin of the TP. Characteristics, sources of PM2.5, and the potential source regions for different chemical components were investigated. During the sampling time, PM2.5 mass loadings ranged from 3.79 to 54.57 µg m−3, with an arithmetic mean concentration of 20.99 ± 9.80 µg m−3. In general, major peaks of organic carbon (OC) and elemental carbon (EC) always coincided with high loadings of K+ and NO3−, which implies that common combustion sources caused these species’ concentrations to covary, while the daily variations of crustal elements showed different trends with the other chemical compositions, suggesting different source regions for crustal materials. Five source factors were identified as possible aerosol sources for PM2.5 by positive matrix factorization (PMF). They are the mining industry (5.3%), characterized by heavy metal elements; secondary formation (18.8%), described by the high concentrations of NH4+ and SO42−; traffic-related emissions (26.7%), dominated by carbonaceous species (especially soot-EC) and some metal elements; fugitive dust (15.2%), represented by crustal elements (Ti, Fe, and Mn), Ca2+, and Mg2+; and biomass burning (34.0%), which is typified by high concentrations of K+, NO3−, char-EC, primary OC, and secondary OC. The concentration-weighted trajectory (CWT) analysis results showed that the northeast part of Burma is the potential source region for high concentrations of EC and NO3− due to biomass burning emissions, while the tourism industry surrounding Gaomeigu gave strong grid cell values of SO42− as well as moderate values of EC and NO3−. Moreover, the mining industry in the southwest direction of Gaomeigu has important impacts on the zinc concentrations.
    Type of Medium: Online Resource
    ISSN: 2073-4433
    Language: English
    Publisher: MDPI AG
    Publication Date: 2019
    detail.hit.zdb_id: 2605928-9
    SSG: 23
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  • 9
    In: Atmosphere, MDPI AG, Vol. 6, No. 2 ( 2015-01-26), p. 164-182
    Type of Medium: Online Resource
    ISSN: 2073-4433
    Language: English
    Publisher: MDPI AG
    Publication Date: 2015
    detail.hit.zdb_id: 2605928-9
    SSG: 23
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  • 10
    In: Atmosphere, MDPI AG, Vol. 8, No. 11 ( 2017-11-08), p. 213-
    Abstract: PM10 samples were collected from Huangshi (HS) city, Central China during April 2012 to March 2013, and were analyzed for short-chain saturated dicarboxylic acids (diacids) using a capillary gas chromatograph (GC). We found that oxalic acid (C2, 318 ± 104 ng·m−3) was the most abundant diacid species, followed by malonic acid (C3, 25.4 ± 9.11 ng·m−3) and succinic acid (C4, 2.09 ± 0.52 ng·m−3). The concentrations of C2 and C4 diacids were highest in winter, followed by summer and spring, and lowest in autumn. C3 diacid was decreased in the order of summer 〉 winter 〉 autumn 〉 spring. Further, the seasonal variations of WSOC (water-soluble organic carbon)- and OC (organic carbon)-normalized diacid concentrations were similar to those of diacid concentrations, suggesting that both primary emission and secondary production are important sources for diacids in Huangshi (HS) aerosols. Strong correlations were found among C2 diacid and the three ions SO42−, NO3−, and NH4+ in summer and winter, suggesting that the species could undergo a similar secondary oxidation processing. C2 had good correlation with K+ in summer and autumn, which indicates an enhanced contribution of combustion sources for C2 diacid. Moreover, according to the ratio of C2/K+, we can conclude that C2 diacid should be formed by a secondary reaction of biomass combustion in HS aerosols, especially in summer and autumn. The ratios of C2/C4 and C3/C4 were compared with those reported in other sites, and the results suggest that HS aerosols should be more photochemically aged than at other urban areas. Principal component analysis of diacids and selected water-soluble inorganic ions over four seasons suggests that HS aerosols are influenced not only from primary emission, but also from secondary reaction. According to the linear relation between C2 and C3 diacids, the results indicate that C2 diacid is formed from the oxidation of hydrocarbon compounds in spring, while it is from the oxidation of C3 and C4 diacids in summer, autumn, and winter.
    Type of Medium: Online Resource
    ISSN: 2073-4433
    Language: English
    Publisher: MDPI AG
    Publication Date: 2017
    detail.hit.zdb_id: 2605928-9
    SSG: 23
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