scholarly journals Modeling the formation of secondary organic aerosol in coastal areas: Role of the sea-salt aerosol organic layer

2003 ◽  
Vol 108 (D15) ◽  
Author(s):  
Xuyi Cai
Keyword(s):  
Secondary Organic Aerosol ◽  
Organic Aerosol ◽  
Coastal Areas ◽  
Sea Salt ◽  
Organic Layer ◽  
Sea Salt Aerosol

scholarly journals Role of sea salt aerosols in the formation of aromatic secondary organic aerosol: yields and hygroscopic properties

2013 ◽  
Vol 10 (3) ◽  
pp. 167 ◽  
Author(s):  
Ross Beardsley ◽  
Myoseon Jang ◽  
Baber Ori ◽  
Yunseok Im ◽  
Carrie A. Delcomyn ◽  
...  
Keyword(s):  
Phase Transition ◽  
Oil Spills ◽  
Secondary Organic Aerosol ◽  
Organic Aerosols ◽  
Organic Aerosol ◽  
Coastal Environment ◽  
Sea Salt ◽  
Hygroscopic Properties ◽  
Inorganic Species

Environmental context In the coastal and ocean environment, oil spills and ship movement can produce hazardous, organic aerosols. In this study, the role of sea salt in the formation processes of crude-oil-derived organic aerosols derived was explored, and it was found that sea salt can greatly increase the formation and growth of these toxic aerosols. Understanding of this process is crucial for evaluating the effect of oil spills and ship movements on air quality and human health. Abstract Dual, large (52m3), outdoor chambers were used to investigate the effect of aerosol aqueous phase chemistry on the secondary organic aerosol (SOA) yields of the photooxidation products of aromatic hydrocarbons in the coastal environment. Toluene and 1,3,5-trimethylbenzene were photochemically oxidised in the presence and absence of inorganic seeds (sea salt aerosol (SSA) or NaCl) at low NOx conditions. Overall, the presence of SSA, which was shown to contain water even at low relative humidities (RHs), led to higher SOA yields than the presence of NaCl seeds and the seedless condition. The results suggest that SOA yields in the coastal environment will be higher than those produced in terrestrial environment. To study the effect of SOA formation on the chemical composition of SSA, inorganic species were measured using a particle-into-liquid-sampler coupled to an ion chromatograph. The hygroscopic properties of the SSA internally mixed with SOA were analysed using a Fourier-transform infrared spectrometer. The fresh SSA shows a weak phase transition whereas no clear phase transition appeared in the aged SSA. The depletion of Cl– due to the accommodation of nitric acid and carboxylic acids on the surface of SSA coincides with changes in aerosol hygroscopic properties.

scholarly journals Aging of atmospheric aerosols and the role of iron in catalyzing brown carbon formation

2021 ◽  
Author(s):  
Hind A. A. Al-Abadleh
Keyword(s):  
Volatile Organic Compounds ◽  
Organic Compounds ◽  
Atmospheric Aerosols ◽  
Secondary Organic Aerosol ◽  
Organic Aerosol ◽  
Atmospheric Oxidation ◽  
Carbon Formation ◽  
Brown Carbon ◽  
Volatile Organic

Extensive research has been done on the processes that lead to the formation of secondary organic aerosol (SOA) including atmospheric oxidation of volatile organic compounds (VOCs) from biogenic and anthropogenic...

Role of stabilized Criegee Intermediate in secondary organic aerosol formation from the ozonolysis of α-cedrene

2014 ◽  
Vol 94 ◽  
pp. 448-457 ◽  
Author(s):  
Lei Yao ◽  
Yan Ma ◽  
Lin Wang ◽  
Jun Zheng ◽  
Alexei Khalizov ◽  
...  
Keyword(s):  
Secondary Organic Aerosol ◽  
Organic Aerosol ◽  
Aerosol Formation ◽  
Secondary Organic Aerosol Formation

scholarly journals Sea-salt aerosol chemistry in coastal areas: A model study

2001 ◽  
Vol 106 (D1) ◽  
pp. 1271-1296 ◽  
Author(s):  
Jana Moldanová ◽  
Evert Ljungström
Keyword(s):  
Coastal Areas ◽  
Sea Salt ◽  
Aerosol Chemistry ◽  
Sea Salt Aerosol ◽  
Model Study

scholarly journals Examining the effects of anthropogenic emissions on isoprene-derived secondary organic aerosol formation during the 2013 Southern Oxidant and Aerosol Study (SOAS) at the Look Rock, Tennessee ground site

2015 ◽  
Vol 15 (15) ◽  
pp. 8871-8888 ◽  
Author(s):  
S. H. Budisulistiorini ◽  
X. Li ◽  
S. T. Bairai ◽  
J. Renfro ◽  
Y. Liu ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Secondary Organic Aerosol ◽  
Organic Aerosol ◽  
Anthropogenic Emissions ◽  
Strongly Correlated ◽  
Particle Phase ◽  
Aerosol Formation ◽  
Aerosol Acidity ◽  
Southeastern Us

Abstract. A suite of offline and real-time gas- and particle-phase measurements was deployed at Look Rock, Tennessee (TN), during the 2013 Southern Oxidant and Aerosol Study (SOAS) to examine the effects of anthropogenic emissions on isoprene-derived secondary organic aerosol (SOA) formation. High- and low-time-resolution PM2.5 samples were collected for analysis of known tracer compounds in isoprene-derived SOA by gas chromatography/electron ionization-mass spectrometry (GC/EI-MS) and ultra performance liquid chromatography/diode array detection-electrospray ionization-high-resolution quadrupole time-of-flight mass spectrometry (UPLC/DAD-ESI-HR-QTOFMS). Source apportionment of the organic aerosol (OA) was determined by positive matrix factorization (PMF) analysis of mass spectrometric data acquired on an Aerodyne Aerosol Chemical Speciation Monitor (ACSM). Campaign average mass concentrations of the sum of quantified isoprene-derived SOA tracers contributed to ~ 9 % (up to 28 %) of the total OA mass, with isoprene-epoxydiol (IEPOX) chemistry accounting for ~ 97 % of the quantified tracers. PMF analysis resolved a factor with a profile similar to the IEPOX-OA factor resolved in an Atlanta study and was therefore designated IEPOX-OA. This factor was strongly correlated (r2 > 0.7) with 2-methyltetrols, C5-alkene triols, IEPOX-derived organosulfates, and dimers of organosulfates, confirming the role of IEPOX chemistry as the source. On average, IEPOX-derived SOA tracer mass was ~ 26 % (up to 49 %) of the IEPOX-OA factor mass, which accounted for 32 % of the total OA. A low-volatility oxygenated organic aerosol (LV-OOA) and an oxidized factor with a profile similar to 91Fac observed in areas where emissions are biogenic-dominated were also resolved by PMF analysis, whereas no primary organic aerosol (POA) sources could be resolved. These findings were consistent with low levels of primary pollutants, such as nitric oxide (NO ~ 0.03 ppb), carbon monoxide (CO ~ 116 ppb), and black carbon (BC ~ 0.2 μg m−3). Particle-phase sulfate is fairly correlated (r2 ~ 0.3) with both methacrylic acid epoxide (MAE)/hydroxymethyl-methyl-α-lactone (HMML)- (henceforth called methacrolein (MACR)-derived SOA tracers) and IEPOX-derived SOA tracers, and more strongly correlated (r2 ~ 0.6) with the IEPOX-OA factor, in sum suggesting an important role of sulfate in isoprene SOA formation. Moderate correlation between the MACR-derived SOA tracer 2-methylglyceric acid with sum of reactive and reservoir nitrogen oxides (NOy; r2 = 0.38) and nitrate (r2 = 0.45) indicates the potential influence of anthropogenic emissions through long-range transport. Despite the lack of a clear association of IEPOX-OA with locally estimated aerosol acidity and liquid water content (LWC), box model calculations of IEPOX uptake using the simpleGAMMA model, accounting for the role of acidity and aerosol water, predicted the abundance of the IEPOX-derived SOA tracers 2-methyltetrols and the corresponding sulfates with good accuracy (r2 ~ 0.5 and ~ 0.7, respectively). The modeling and data combined suggest an anthropogenic influence on isoprene-derived SOA formation through acid-catalyzed heterogeneous chemistry of IEPOX in the southeastern US. However, it appears that this process was not limited by aerosol acidity or LWC at Look Rock during SOAS. Future studies should further explore the extent to which acidity and LWC as well as aerosol viscosity and morphology becomes a limiting factor of IEPOX-derived SOA, and their modulation by anthropogenic emissions.

scholarly journals Secondary organic aerosol production from modern diesel engine emissions

2009 ◽  
Vol 9 (4) ◽  
pp. 17665-17704 ◽  
Author(s):  
S. Samy ◽  
B. Zielinska
Keyword(s):  
Secondary Organic Aerosol ◽  
Dicarboxylic Acids ◽  
Transformation Products ◽  
Organic Aerosol ◽  
Engine Emissions ◽  
No3 Radical ◽  
Group Basis ◽  
Chamber Studies ◽  
The Impact

Abstract. Secondary organic aerosol (SOA) production was observed at significant levels in a series of modern diesel exhaust (DE) aging experiments conducted at the European Outdoor Photoreactor/Simulation Chamber (EUPHORE). The greatest production occurred in DE with toluene addition experiments (>40%), followed by DE with HCHO (for OH radical generation) experiments. A small amount of SOA (3%) was observed for DE in dark with N2O5 (for NO3 radical production) experiments. The analysis for a limited number (54) of polar organic compounds (POC) was conducted to assess the composition of modern DE and the formation of photochemical transformation products. Distinct POC formation in light versus dark experiments suggests the role of OH initiated reactions in these chamber atmospheres. A trend of increasing concentrations of dicarboxylic acids in light versus dark experiments was observed when evaluated on a compound group basis. The four toluene addition experiments in this study were performed at different [tol]o/[NOx]o ratios and displayed an average SOA% yield (in relation to toluene) of 5.3±1.6%, which is compared to past chamber studies that evaluated the impact of [tol]o/[NOx]o on SOA production in more simplified mixtures.

scholarly journals Determination of aerosol fraction distribution in Viet Nam based on LIDAR monitoring data and back-trajectory statistical methods

2017 ◽  
Vol 1 (T3) ◽  
pp. 64-67
Author(s):  
Binh Thanh Nguyen ◽  
Hoang Dinh Nguyen ◽  
Tuan Xuan Nguyen ◽  
Trung Van Dinh ◽  
Bich Thi Vu ◽  
...  
Keyword(s):  
Statistical Methods ◽  
Organic Aerosol ◽  
Sea Salt ◽  
Aerosol Concentration ◽  
Monitoring Data ◽  
Back Trajectory ◽  
North West ◽  
Sea Salt Aerosol ◽  
Fraction Distribution ◽  
Aerosol Fraction

The aerosol fraction distribution in Vietnam was determined based on monitoring data LIDAR at Hanoi and GEOS–Chem using back-trajectory statistical methods. The results showed that the aerosol concentration is the highest in northeastern of Vietnam and decreasing in the southern and western directions. Maximum of organic aerosol concentration is on the north-west. The highest sea salt aerosol concentrations are in East sea and Bengal bay. Aerosol consists mainly of sulfate, organic aerosol, and sea salt aerosol: sulfate, nitrate, black carbon, ammonium, mineral dust aerosol… The result shows the complicated aerosol distribution in Vietnam.

scholarly journals Impact of NO<sub>x</sub> on secondary organic aerosol (SOA) formation from <i>α</i>-pinene and <i>β</i>-pinene photo-oxidation: the role of highly oxygenated organic nitrates

2020 ◽  
Author(s):  
Iida Pullinen ◽  
Sebastian Schmitt ◽  
Sungah Kang ◽  
Mehrnaz Sarrafzadeh ◽  
Patrick Schlag ◽  
...  
Keyword(s):  
Gas Phase ◽  
Functional Groups ◽  
Secondary Organic Aerosol ◽  
Organic Aerosol ◽  
Organic Nitrate ◽  
Organic Nitrates ◽  
Peroxy Radicals ◽  
Photo Oxidation ◽  
Mass Formation

Abstract. The formation of organic nitrates (ON) in the gas phase and their impact on mass formation of Secondary Organic Aerosol (SOA) was investigated in a laboratory study for α-pinene and β-pinene photo-oxidation. Focus was the elucidation of those mechanisms that cause the often observed suppression of SOA mass formation by NOx, and therein the role of highly oxygenated multifunctional molecules (HOM). We observed that with increasing NOx (a) the portion of HOM organic nitrates (HOM-ON) increased, (b) the fraction of accretion products (HOM-ACC) decreased and (c) HOM-ACC contained on average smaller carbon numbers. Specifically, we investigated HOM organic nitrates (HOM-ON), arising from the termination reactions of HOM peroxy radicals with NOx, and HOM permutation products (HOM-PP), such as ketones, alcohols or hydroperoxides, formed by other termination reactions. Effective uptake coefficients γeff of HOM on particles were determined. HOM with more than 6 O-atoms efficiently condensed on particles (γeff > 0.5 in average) and for HOM containing more than 8 O-atoms, every collision led to loss. There was no systematic difference in γeff for HOM-ON and HOM-PP arising from the same HOM peroxy radicals. This similarity is attributed to the multifunctional character of the HOM: as functional groups in HOM arising from the same precursor HOM peroxy radical are identical, vapor pressures should not strongly depend on the character the final termination group. As a consequence, the suppressing effect of NOx on SOA formation cannot be simply explained by replacement of terminal functional groups by organic nitrate groups. The fraction of organic bound nitrate (OrgNO3) stored in gas-phase HOM-ON appeared to be substantially higher than the fraction of particulate OrgNO3 observed by aerosol mass spectrometry. This result suggests losses of OrgNO3 for organic nitrates in particles, probably due to hydrolysis of OrgNO3 that releases HNO3 into the gas phase but leaves behind the organic rest in the particulate phase. However, the loss of HNO3 alone, could not explain the observed suppressing effect of NOx on particle mass formation from α-pinene and β-pinene. We therefore attributed most of the reduction in SOA mass yields with increasing NOx to the significant suppression of gas-phase HOM-ACC which have high molecular mass and are potentially important for SOA mass formation at low NOx conditions.

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