scholarly journals Diurnal and day-to-day characteristics of ambient particle mass size distributions from HR-ToF-AMS measurements at an urban site and a suburban site in Hong Kong

2017 ◽  
Author(s):  
Berto P. Lee ◽  
Hao Wang ◽  
Chak K. Chan
Keyword(s):  
Particle Size ◽  
Hong Kong ◽  
Particle Mass ◽  
Urban Site ◽  
Size Distributions ◽  
Particle Size Distributions ◽  
Accumulation Mode ◽  
Ambient Particle ◽  
Mass Median ◽  
Suburban Site

Abstract. Mass concentration based particle size distributions measured by a high-resolution aerosol mass spectrometer were systematically analyzed to assess long and short-term temporal characteristics of ambient particle size distributions sampled at a typical urban environment close to emission sources and a suburban coastal site representing a regional and local pollution receptor location in Hong Kong. Measured distributions were bimodal and deconvoluted into submodes which were analyzed for day-to-day variations and diurnal variations. Traffic and cooking emissions at the urban site contributed substantially to particle mass in both modes, while notable decreases in mass median diameters were limited to the morning rush hour. Inorganic particle components displayed varying diurnal behavior, including nocturnal nitrate formation and daytime photochemical formation evident in both modes. Suburban particle size distributions exhibited notable seasonal disparities with differing influence of local formation, particularly in spring and summer, and transport which dominated in the fall season leading to notably higher sulfate and organic accumulation mode particle concentrations. Variations in particle mixing state were evaluated by comparison of inter-species mass median diameter trends at both measurement sites. Internal mixing was prevalent in the accumulation mode in spring at the urban site, while greater frequency of time periods with external mixing of particle populations comprising different fractions of organic constituents was observed in summer. At the suburban site, sulfate and nitrate in the accumulation mode more frequently exhibited differing particle size distributions in all seasons signifying a greater extent of external mixing. At the urban site, periods of greater submicron inorganic mass concentrations were more likely to be caused by increases in both Aitken and accumulation mode particle mass in summer, while at the suburban receptor location organic and nitrate Aitken mode particle mass contributed more regularly to higher total submicron species mass concentrations in most seasons (spring, summer and winter).

scholarly journals Diurnal and day-to-day characteristics of ambient particle mass size distributions from HR-ToF-AMS measurements at an urban site and a suburban site in Hong Kong

2017 ◽  
Vol 17 (22) ◽  
pp. 13605-13624 ◽  
Author(s):  
Berto Paul Lee ◽  
Hao Wang ◽  
Chak Keung Chan
Keyword(s):  
Particle Size ◽  
Hong Kong ◽  
Particle Mass ◽  
Urban Site ◽  
Size Distributions ◽  
Particle Size Distributions ◽  
Accumulation Mode ◽  
Ambient Particle ◽  
Mass Median ◽  
Suburban Site

Abstract. Mass-concentration-based particle size distributions measured by a high-resolution aerosol mass spectrometer were systematically analyzed to assess long and short-term temporal characteristics of ambient particle size distributions sampled at a typical urban environment close to emission sources and a suburban coastal site representing a regional and local pollution receptor location in Hong Kong. Measured distributions were bimodal and deconvoluted into submodes, which were analyzed for day-to-day variations and diurnal variations. Traffic and cooking emissions at the urban site contributed substantially to particle mass in both modes, while notable decreases in mass median diameters were limited to the morning rush hour. Inorganic particle components displayed varying diurnal behavior, including nocturnal nitrate formation and daytime photochemical formation evident in both modes. Suburban particle size distributions exhibited notable seasonal disparities with differing influence of local formation, particularly in spring and summer, and transport which dominated in the fall season leading to notably higher sulfate and organic accumulation-mode particle concentrations. Variations in particle mixing state were evaluated by comparison of interspecies mass median diameter trends at both measurement sites. Internal mixing was prevalent in the accumulation mode in spring at the urban site, while greater frequency of time periods with external mixing of particle populations comprising different fractions of organic constituents was observed in summer. At the suburban site, sulfate and nitrate in the accumulation mode more frequently exhibited differing particle size distributions in all seasons, signifying a greater extent of external mixing. At the urban site, periods of greater submicron inorganic mass concentrations were more likely to be caused by increases in both Aitken- and accumulation-mode particle mass in summer, while at the suburban receptor location, organic and nitrate Aitken-mode particle mass contributed more regularly to higher total submicron species mass concentrations in most seasons (spring, summer, and winter).

scholarly journals Particle size distribution of nitrated and oxygenated polycyclic aromatic hydrocarbons (NPAHs and OPAHs) on traffic and suburban sites of a European megacity: Paris (France)

2012 ◽  
Vol 12 (18) ◽  
pp. 8877-8887 ◽  
Author(s):  
J. Ringuet ◽  
E. Leoz-Garziandia ◽  
H. Budzinski ◽  
E. Villenave ◽  
A. Albinet
Keyword(s):  
Particle Size ◽  
Polycyclic Aromatic Hydrocarbons ◽  
Size Distribution ◽  
Aromatic Hydrocarbons ◽  
Size Distributions ◽  
Particle Size Distributions ◽  
Oxygenated Polycyclic Aromatic Hydrocarbons ◽  
Polycyclic Aromatic ◽  
Traffic Site ◽  
Suburban Site

Abstract. The size distribution of particulate nitrated and oxygenated polycyclic aromatic hydrocarbons (NPAHs and OPAHs) was determined during two field campaigns at a traffic site in summer 2010 and at a suburban site during the MEGAPOLI (Megacities: Emissions, urban, regional and Global Atmospheric POLlution and climate effects, and Integrated tools for assessment and mitigation) experiment in summer 2009. Both, OPAHs and NPAHs were strongly associated (>85%) to fine particles (Dp< 2.5 μm) increasing the interest of their study on a sanitary point of view. Results showed really different NPAH and OPAH particle size distributions between both sites. At traffic site, clearly bimodal (notably for NPAHs) particle size distributions (Dp = 0.14 and 1.4 μm) were observed, while the particle size distributions were more scattered at the suburban site, especially for OPAHs. Bimodal particle size distribution observed at traffic site for the NPAH could be assigned to the vehicle emissions and the particle resuspension. Broadest distribution observed at the suburban site could be attributed to the mass transfer of compounds by volatilization/sorption processes during the transport of particles in the atmosphere. Results also showed that the combination of the study of particle size distributions applied to marker compounds (primary: 1-nitropyrene; secondary: 2-nitrofluoranthene) and to NPAH or OPAH chemical profiles bring some indications on their primary and/or secondary origin. Indeed, 1,4-anthraquinone seemed only primary emitted by vehicles while 7-nitrobenz[a]anthracene, benz[a]antracen7,12-dione and benzo[b]fluorenone seemed secondarily formed in the atmosphere.

scholarly journals Measurement report: Vertical profiling of particle size distributions over Lhasa, Tibet: Tethered balloon-based in-situ measurements and source apportionment

2021 ◽  
Author(s):  
Liang Ran ◽  
Zhaoze Deng ◽  
Yunfei Wu ◽  
Jiwei Li ◽  
Zhixuan Bai ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Particle Size ◽  
Source Apportionment ◽  
Particle Mass ◽  
Size Distributions ◽  
Aerosol Formation ◽  
Tethered Balloon ◽  
Particle Size Distributions ◽  
Secondary Aerosol

Abstract. In-situ measurements of vertically resolved particle size distributions based on a tethered balloon system were carried out for the first time in the highland city of Lhasa over the Tibetan Plateau in summer 2020, using portable optical counters for the size range of 0.124~32 μm. The vertical structure of 112 aerosol profiles was found to be largely shaped by the evolution of the boundary layer (BL), with a nearly uniform distribution of aerosols within the daytime mixing layer and a sharp decline with the height in the shallow nocturnal boundary layer. During the campaign, the average mass concentration of particulate matters smaller than 2.5 μm in aerodynamic diameter (PM2.5) within the BL was around 3 μg m−3, almost four times of the amount in the free troposphere (FT), which was rarely affected by surface anthropogenic emissions. Though there was a lower level of particle mass in the residual layer (RL) than in the BL, a similarity in particle mass size distributions (PMSDs) suggested that particles in the RL might be of the same origin as particles in the BL. This was also in consistence with the source apportionment analysis based on the PMSDs. Three distinct modes were observed in the PMSDs for the BL and the RL. One mode was exclusively coarse particles up to roughly 15 μm and peaked around 5 μm. More than 50 % of total particle mass was often contributed by coarse mode particles in this area, which was thought to be associated with local dust resuspension. The mode peaking over 0.5~0.7 μm was representative of biomass burning on religious holidays and was found to be most pronounced on holiday mornings. The contribution from the religious burning factor rose from about 25 % on non-holidays to nearly 50 % on holiday mornings. The mode dominated by particles smaller than 0.3 μm was thought to be associated with combustion related emissions and/or secondary aerosol formation. In the FT coarse mode particles only accounted for less than 10 % of the total mass and particles larger than 5 μm were negligible. The predominant submicron particles in the FT might be related to secondary aerosol formation and the aging of existed particles. To give a full picture of aerosol physical and chemical properties and better understand the origin and impacts of aerosols in this area, intensive field campaigns involving measurements of vertically resolved aerosol chemical compositions in different seasons would be much encouraged in the future.

scholarly journals Physical and chemical properties of the regional mixed layer of Mexico's Megapolis Part II: evaluation of measured and modeled trace gases and particle size distributions

2012 ◽  
Vol 12 (21) ◽  
pp. 10161-10179 ◽  
Author(s):  
C. Ochoa ◽  
D. Baumgardner ◽  
M. Grutter ◽  
J. Allan ◽  
J. Fast ◽  
...  
Keyword(s):  
Particle Size ◽  
Standard Deviation ◽  
Transport Model ◽  
Trace Gases ◽  
Research Station ◽  
Size Distributions ◽  
Particle Size Distributions ◽  
Air Masses ◽  
Accumulation Mode ◽  
Mountain Site

Abstract. This study extends the work of Baumgardner et al. (2009) in which measurements of trace gases and particles, at a remote, high altitude mountain site, 60 km from Mexico City were analyzed with respect to the origin of the air masses. In the current evaluation, the temperature, water vapor mixing ratio (WMR), ozone (O3), carbon monoxide (CO), sulfur dioxide (SO2) and acyl peroxy nitrate (APN) are simulated with the WRF-Chem chemical transport model and compared with the measurements at the mountain site. Comparisons between the model and measurements are also evaluated for particle size distributions (PSDs) of the mass concentrations of sulfate, nitrate, ammonium and organic mass (OM). The model predictions of the diurnal trends in temperature, WMR and trace gases were generally well correlated; 13 of the 18 correlations were significant at a confidence level of <0.01. Less satisfactory were the average hourly differences between model and measurements that showed predicted values within expected, natural variation for only 10 of the 18 comparisons. The model performed best when comparing with the measurements during periods when the air originated from the east. In that case all six of the parameters being compared had average differences between the model and measurements less than the expected standard deviation. For the cases when the air masses are from the southwest or west northwest, only two of the comparisons from each case showed differences less than the expected standard deviation. The differences appear to be a result of an overly rapid growth of the boundary layer predicted by the model and too much dilution. There also is more O3 being produced, most likely by photochemical production, downwind of the emission sources than is predicted by the model. The measured and modeled PSD compare very well with respect to their general shape and the diameter of the peak concentrations. The spectra are log normally distributed with most of the mass in the accumulation mode centered at 200 ± 20 nm and little observed or predicted changes with respect to the time when the RML is above the Altzomoni research station. Only the total mass changes with time and air mass origin. The invariability of average diameter of the accumulation mode suggests that there is very little growth of the particles by condensation or coagulation after six hours of aging downwind of the major sources of anthropogenic emissions in Mexico's Megapolis. This could greatly simplify parameterization in climate models although it is not known at this time if this invariance can be extended to other megacity regions.

Sign in / Sign up

Export Citation Format

Share Document