scholarly journals Observations of Particles at their Formation Sizes in Beijing, China

Author(s):  
Rohan Jayaratne ◽  
Buddhi Pushpawela ◽  
Congrong He ◽  
Jian Gao ◽  
Li Hui ◽  
...  

Abstract. New particle formation (NPF) has been observed in many highly polluted environments of South-East Asia, including Beijing, where the extent of its contribution to intense haze events is still an open question. Estimated characteristics of NPF events, such as their starting times and formation and growth rates of particles, are very different when the measurements are restricted to particles in larger size ranges. In order to understand the very first steps of particle formation, we used a neutral cluster and air ion spectrometer (NAIS) to investigate particle characteristics at sizes exactly where atmospheric nucleation and cluster activity occurs. Observations over a continuous three-month period in Beijing showed 26 NPF events. These events generally coincided with periods with relatively clean air when the wind direction was from the less-industrialized north. No NPF were observed when the daily mean PM2.5 concentration exceeded 43 µg m-3, which was the upper threshold for particle formation in Beijing. The fraction of particles that are charged in the size range 2–42 nm was normally about 15%. However, this fraction increased to 20–30% during haze events and decreased to below 10 % during NPF events. With the NAIS, we determined the starting times of NPF very precisely to a greater accuracy than has been possible in Beijing before and provided a temporal distribution of NPF events with a maximum at about 8.30 am. Particle formation rates varied between 10–36 cm-3 s-1. Particle growth rates were estimated to be in the range 0.5–9.0 nm h-1. These results are more reliable than previous studies in Beijing as the measurements were conducted for the first time at the exact sizes where clusters form into particles and provide useful insight into the formation of haze events.

2017 ◽  
Vol 17 (14) ◽  
pp. 8825-8835 ◽  
Author(s):  
Rohan Jayaratne ◽  
Buddhi Pushpawela ◽  
Congrong He ◽  
Hui Li ◽  
Jian Gao ◽  
...  

Abstract. New particle formation (NPF) has been observed in many highly polluted environments of South East Asia, including Beijing, where the extent of its contribution to intense haze events is still an open question. Estimated characteristics of NPF events, such as their starting times and formation and growth rates of particles, are more accurate when the detection range of particles extends to smaller sizes. In order to understand the very first steps of particle formation, we used a neutral cluster and air ion spectrometer (NAIS) to investigate particle characteristics at sizes exactly at which atmospheric nucleation and cluster activity occurs. Observations over a continuous 3-month period in Beijing showed 26 NPF events. These events generally coincided with periods with relatively clean air when the wind direction was from the less industrialised north. No NPF events were observed when the daily mean PM2. 5 concentration exceeded 43 µg m−3, which was the upper threshold for particle formation in Beijing. The fraction of particles that are charged in the size range 2–42 nm was normally about 15 %. However, this fraction increased to 20–30 % during haze events and decreased to below 10 % during NPF events. With the NAIS, we very precisely determined the starting times of NPF to a greater accuracy than has been possible in Beijing before and provided a temporal distribution of NPF events with a maximum at about 08:30 LT. Particle formation rates varied between 12 and 38 cm−3 s−1. Particle growth rates were estimated to be in the range of 0.5–9.0 nm h−1. These results are more reliable than previous studies in Beijing as the measurements were conducted for the first time at the exact sizes at which clusters form into particles and provide useful insight into the formation of haze events.


2014 ◽  
Vol 14 (8) ◽  
pp. 3865-3881 ◽  
Author(s):  
M. I. García ◽  
S. Rodríguez ◽  
Y. González ◽  
R. D. García

Abstract. A climatology of new particle formation (NPF) events at high altitude in the subtropical North Atlantic is presented. A 4-year data set (June 2008–June 2012), which includes number size distributions (10–600 nm), reactive gases (SO2, NOx, and O3), several components of solar radiation and meteorological parameters, measured at Izaña Global Atmosphere Watch (GAW) observatory (2373 m above sea level; Tenerife, Canary Islands) was analysed. NPF is associated with the transport of gaseous precursors from the boundary layer by orographic buoyant upward flows that perturb the low free troposphere during daytime. On average, 30% of the days contained an NPF event. Mean values of the formation and growth rates during the study period were 0.46 cm−3 s−1 and 0.42 nm h−1, correspondingly. There is a clearly marked NPF season (May–August), when these events account for 50–60% of the days per month. Monthly mean values of the formation and growth rates exhibit higher values in this season, 0.49–0.92 cm−3 s−1 and 0.48–0.58 nm h−1, respectively. During NPF events, SO2, UV radiation and upslope winds showed higher values than during non-events. The overall data set indicates that SO2 plays a key role as precursor, although other species seem to contribute during some periods. Condensation of sulfuric acid vapour accounts for most of the measured particle growth during most of the year (~70%), except for some periods. In May, the highest mean growth rates (~0.6 nm h−1) and the lowest contribution of sulfuric acid (~13%) were measured, suggesting a significant involvement of other condensing vapours. The SO2 availability seems also to be the most influencing parameter in the year-to-year variability in the frequency of NPF events. The condensation sink showed similar features to other mountain sites, showing high values during NPF events. Summertime observations, when Izaña is within the Saharan Air Layer, suggest that dust particles may play a significant role acting as coagulation sink of freshly formed nucleation particles. The contribution of dust particles to the condensation sink of sulfuric acid vapours seems to be modest (~8% as average). Finally, we identified a set of NPF events in which two nucleation modes, which may evolve at different rates, occur simultaneously and for which further investigations are necessary.


2005 ◽  
Vol 5 (7) ◽  
pp. 1773-1785 ◽  
Author(s):  
V. Fiedler ◽  
M. Dal Maso ◽  
M. Boy ◽  
H. Aufmhoff ◽  
J. Hoffmann ◽  
...  

Abstract. Atmospheric gaseous sulphuric acid was measured and its influence on particle formation and growth was investigated building on aerosol data. The measurements were part of the EU-project QUEST and took place at two different measurement sites in Northern and Central Europe (Hyytiälä, Finland, March-April 2003 and Heidelberg, Germany, March-April 2004). From a comprehensive data set including sulphuric acid, particle number size distributions and meteorological data, particle growth rates, particle formation rates and source rates of condensable vapors were inferred. Growth rates were determined in two different ways, from particle size distributions as well as from a so-called timeshift analysis. Moreover, correlations between sulphuric acid and particle number concentration between 3 and 6 nm were examined and the influence of air masses of different origin was investigated. Measured maximum concentrations of sulphuric acid were in the range from 1x106 to 16x106cm-3. The gaseous sulphuric acid lifetime with respect to condensation on aerosol particles ranged from 2 to 33min in Hyytiälä and from 0.5 to 8 min in Heidelberg. Most calculated values (growth rates, formation rates, vapor source rates) were considerably higher in Central Europe (Heidelberg), due to the more polluted air and higher preexistent aerosol concentrations. Close correlations between H2SO4 and nucleation mode particles (size range: 3-6 nm) were found on most days at both sites. The percentage contribution of sulphuric acid to particle growth was below 10% at both places and to initial growth below 20%. An air mass analysis indicated that at Heidelberg new particles were formed predominantly in air advected from southwesterly directions.


2005 ◽  
Vol 5 (6) ◽  
pp. 11929-11963 ◽  
Author(s):  
M. Komppula ◽  
S.-L. Sihto ◽  
H. Korhonen ◽  
H. Lihavainen ◽  
V.-M. Kerminen ◽  
...  

Abstract. This study covers four years of aerosol number size distribution data from Pallas and Värriö sites 250 km apart from each other in Northern Finland and compares new particle formation events between these sites. In eastern air masses almost all events were observed to start earlier at the eastern station Värriö, whereas in western air masses most of the events were observed to start earlier at the western station Pallas. This demonstrates that particle formation in a certain air mass type depends not only on the diurnal variation of the parameters causing the phenomenon (such as photochemistry) but also on some properties carried by the air mass itself. The correlation in growth rates between the two sites was relatively good, which suggests that the amount of condensable vapour causing the growth must have been at about the same level in both sites. The value of condensation sink was frequently much higher at the downwind station. It seems that secondary particle formation related to biogenic sources dominate in many cases over the particle sinks during the air mass transport between the sites. Two cases of transport from Pallas to Värriö were further analysed with an aerosol dynamics model. The model was able to reproduce the observed nucleation events 250 km down-wind at Värriö but revealed some differences between the two cases. The simulated nucleation rates were in both cases similar but the organic concentration profiles that best reproduced the observations were different in the two cases indicating that divergent formation reactions may dominate under different conditions. The simulations also suggested that organic compounds were the main contributor to new particle growth, which offers a tentative hypothesis to the distinct features of new particles at the two sites: Air masses arriving from Atlantic Ocean typically spent approximately only ten hours over land before arriving at Pallas, and thus the time for the organic vapours to accumulate in the air and to interact with the particles is relatively short. This can lead to low nucleation mode growth rates and even to suppression of detectable particle formation event due to efficient scavenging of newly formed clusters, as was observed in the case studies.


2008 ◽  
Vol 8 (2) ◽  
pp. 6313-6353 ◽  
Author(s):  
L. Laakso ◽  
H. Laakso ◽  
P. P. Aalto ◽  
P. Keronen ◽  
T. Petäjä ◽  
...  

Abstract. We have analyzed one year (July 2006–July 2007) of measurement data from a relatively clean background site located in dry savannah in South Africa. The annual-median trace gas concentrations were equal to 0.7 ppb for SO2, 1.4 ppb for NOx, 36 ppb for O3 and 105 ppb for CO. The corresponding PM1, PM2.5 and PM10 concentrations were 9.0, 10.5 and 18.8 μg m−3, and the annual median total particle number concentration in the size range 10–840 nm was 2340 cm−3. Gases and particles had a clear seasonal and diurnal variation, which was associated with field fires and biological activity together with local meteorology. Atmospheric new-particle formation was observed to take place in more than 90% of the analyzed days. The days with no new particle formation were cloudy or rainy days. The formation rate of 10 nm particles varied in the range of 0.1–28 cm−3 s−1 (median 1.9 cm−3 s−1) and nucleation mode particle growth rates were in the range 3–21 nm h−1 (median 8.5 nm h−1). Due to high formation and growth rates, observed new particle formation gives a significant contribute to the number of cloud condensation nuclei budget, having a potential to affect the regional climate forcing patterns.


2019 ◽  
Vol 19 (8) ◽  
pp. 5679-5694 ◽  
Author(s):  
Dimitrios Bousiotis ◽  
Manuel Dall'Osto ◽  
David C. S. Beddows ◽  
Francis D. Pope ◽  
Roy M. Harrison

Abstract. New particle formation (NPF) events have different patterns of development depending on the conditions of the area in which they occur. In this study, particle size distributions in the range of 16.6–604 nm (7 years of data) were analysed and NPF events occurring at three sites of differing characteristics – rural Harwell (HAR), urban background North Kensington (NK), urban roadside Marylebone Road (MR), London, UK – were extracted and studied. The different atmospheric conditions in each study area not only have an effect on the frequency of the events, but also affect their development. The frequency of NPF events is similar at the rural and urban background locations (about 7 % of days), with a high proportion of events occurring at both sites on the same day (45 %). The frequency of NPF events at the urban roadside site is slightly less (6 % of days), and higher particle growth rates (average 5.5 nm h−1 at MR compared to 3.4 and 4.2 nm h−1 at HAR and NK respectively) must result from rapid gas-to-particle conversion of traffic-generated pollutants. A general pattern is found in which the condensation sink increases with the degree of pollution of the site, but this is counteracted by increased particle growth rates at the more polluted location. A key finding of this study is that the role of the urban environment leads to an increment of 20 % in N16–20 nm in the urban background compared to that of the rural area in NPF events occurring at both sites. The relationship of the origin of incoming air masses is also considered and an association of regional events with cleaner air masses is found. Due to lower availability of condensable species, NPF events that are associated with cleaner atmospheric conditions have lower growth rates of the newly formed particles. The decisive effect of the condensation sink in the development of NPF events and the survivability of the newly formed particles is underlined, and influences the overall contribution of NPF events to the number of ultrafine particles in an area. The other key factor identified by this study is the important role that pollution, both from traffic and other sources in the urban environment (such as heating or cooking), plays in new particle formation events.


2010 ◽  
Vol 10 (17) ◽  
pp. 8469-8480 ◽  
Author(s):  
C. Kuang ◽  
I. Riipinen ◽  
S.-L. Sihto ◽  
M. Kulmala ◽  
A. V. McCormick ◽  
...  

Abstract. A dimensionless theory for new particle formation (NPF) was developed, using an aerosol population balance model incorporating recent developments in nucleation rates and measured particle growth rates. Based on this theoretical analysis, it was shown that a dimensionless parameter LΓ, characterizing the ratio of the particle scavenging loss rate to the particle growth rate, exclusively determined whether or not NPF would occur on a particular day. This parameter determines the probability that a nucleated particle will grow to a detectable size before being lost by coagulation with the pre-existing aerosol. Cluster-cluster coagulation was shown to contribute negligibly to this survival probability under conditions pertinent to the atmosphere. Data acquired during intensive measurement campaigns in Tecamac (MILAGRO), Atlanta (ANARChE), Boulder, and Hyytiälä (QUEST II, QUEST IV, and EUCAARI) were used to test the validity of LΓ as an NPF criterion. Measurements included aerosol size distributions down to 3 nm and gas-phase sulfuric acid concentrations. The model was applied to seventy-seven NPF events and nineteen non-events (characterized by growth of pre-existing aerosol without NPF) measured in diverse environments with broad ranges in sulfuric acid concentrations, ultrafine number concentrations, aerosol surface areas, and particle growth rates (nearly two orders of magnitude). Across this diverse data set, a nominal value of LΓ=0.7 was found to determine the boundary for the occurrence of NPF, with NPF occurring when LΓ<0.7 and being suppressed when LΓ>0.7. Moreover, nearly 45% of measured LΓ values associated with NPF fell in the relatively narrow range of 0.1


2021 ◽  
Vol 753 ◽  
pp. 142207
Author(s):  
Biwu Chu ◽  
Lubna Dada ◽  
Yongchun Liu ◽  
Lei Yao ◽  
Yonghong Wang ◽  
...  

2012 ◽  
Vol 12 (5) ◽  
pp. 11351-11389 ◽  
Author(s):  
F. Riccobono ◽  
L. Rondo ◽  
M. Sipilä ◽  
P. Barmet ◽  
J. Curtius ◽  
...  

Abstract. Lack of knowledge about the mechanisms underlying new particle formation and their subsequent growth is one of the main causes for the large uncertainty in estimating the radiative forcing of atmospheric aerosols in global models. We performed chamber experiments designed to study the contributions of sulfuric acid and organic vapors to formation and to the early growth of nucleated particles, respectively. Distinct experiments in the presence of two different organic precursors (1,3,5-trimethylbenzene and α-pinene) showed the ability of these compounds to reproduce the formation rates observed in the low troposphere. These results were obtained measuring the sulfuric acid concentrations with two Chemical Ionization Mass Spectrometers confirming the results of a previous study which modeled the sulfuric acid concentrations in presence of 1,3,5-trimethylbenzene. New analysis methods were applied to the data collected with a Condensation Particle Counter battery and a Scanning Mobility Particle Sizer, allowing the assessment of the size resolved growth rates of freshly nucleated particles. The effect of organic vapors on particle growth was investigated by means of the growth rate enhancement factor (Γ), defined as the ratio between the measured growth rate in the presence of α-pinene and the kinetically limited growth rate of the sulfuric acid and water system. The observed Γ values indicate that the growth is dominated by organic compounds already at particle diameters of 2 nm. Both the absolute growth rates and Γ showed a strong dependence on particle size supporting the nano-Köhler theory. Moreover, the separation of the contributions from sulfuric acid and organic compounds to particles growth reveals that the organic contribution seems to be enhanced by the sulfuric acid concentration. The size resolved growth analysis finally indicates that both condensation of oxidized organic compounds and reactive uptake contribute to particle growth.


2010 ◽  
Vol 10 (1) ◽  
pp. 491-521 ◽  
Author(s):  
C. Kuang ◽  
I. Riipinen ◽  
S.-L. Sihto ◽  
M. Kulmala ◽  
A. V. McCormick ◽  
...  

Abstract. A dimensionless theory for new particle formation (NPF) was developed, using an aerosol population balance model incorporating recent developments in nucleation rates and measured particle growth rates. Based on this theoretical analysis, it was shown that a dimensionless parameter LΓ, characterizing the ratio of the particle scavenging loss rate to the particle growth rate, exclusively determined whether or not NPF would occur on a particular day. This parameter determines the probability that a nucleated particle will grow to a detectable size before being lost by coagulation with the pre-existing aerosol. Cluster-cluster coagulation was shown to contribute negligibly to this survival probability under conditions pertinent to the atmosphere. Data acquired during intensive measurement campaigns in Tecamac (MILAGRO), Atlanta (ANARChE), Boulder, and Hyytiälä (QUEST II, QUEST IV, and EUCAARI) were used to test the validity of LΓ as an NPF criterion. Measurements included aerosol size distributions down to 3 nm and gas-phase sulfuric acid concentrations. The model was applied to seventy-seven NPF events and nineteen non-events (characterized by growth of pre-existing aerosol without NPF) measured in diverse environments with broad ranges in sulfuric acid concentrations, ultrafine number concentrations, aerosol surface areas, and particle growth rates (nearly two orders of magnitude). Across this diverse data set, a nominal value of LΓ=0.7 was found to determine the boundary for the occurrence of NPF, with NPF occurring when LΓ<0.7 and being suppressed when LΓ> 0.7. Moreover, nearly 45% of measured LΓ values associated with NPF fell in the relatively narrow range of 0.1<LΓ<0.3.


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