| 1. |
- Crljenica, Ivica, et al.
(författare)
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Determining the saturation vapour pressures of keto-dicarboxylic acids in aqueous solutions
- 2013
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Ingår i: NUCLEATION AND ATMOSPHERIC AEROSOLS. - : American Institute of Physics (AIP). - 9780735411524 ; , s. 468-471
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Konferensbidrag (refereegranskat)abstract
- A two-compartment binary mass transport model with group contribution methods parametrizations for the physical properties of the organic acids (UNIFAC Dortmund method for activity coefficients, GCVOL-OL-60 method for the pure liquid acid density, GC-MG method for the pure acid surface tension at room temperature, Fuller et al. method for the diffusion coefficients) was used to interpret the evaporation experiments of 100 nm sized keto-dicarboxylic acid aqueous solutions droplets at ambient temperature. The determined values for the saturation vapour pressure of liquid 2-keto-glutaric acid are in the order of 10(-5) Pa.
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| 2. |
- D'Andrea, S. D., et al.
(författare)
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Effect of Secondary Organic Aerosol Amount and Condensational Behavior on Global Aerosol Size Distributions
- 2013
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Ingår i: NUCLEATION AND ATMOSPHERIC AEROSOLS. - : American Institute of Physics (AIP). - 9780735411524 ; , s. 667-670
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Konferensbidrag (refereegranskat)abstract
- Recent research has shown that secondary organic aerosols (SOA) are major contributors to ultrafine particle growth to climatically relevant sizes, increasing global cloud condensation nuclei (CCN) concentrations within the continental boundary layer. Many models treat SOA solely as semivolatile, which leads to condensation of SOA proportional to the aerosol mass distribution; however, recent closure studies with field measurements show that a significant fraction of SOA condenses proportional to the aerosol surface area, which suggests a very low volatility. Additionally, while many global models contain only biogenic sources of SOA (with emissions generally 10-30 Tg yr(-1)), recent studies have shown a need for an additional source of SOA around 100 Tg yr(-1) correlated with anthropogenic carbon monoxide (CO) emissions is required to match measurements. Here, we explore the significance of these two findings using the GEOS-Chem-TOMAS global aerosol microphysics model. The percent change in the number of particles of size D-p > 40 nm (N40) within the continental boundary layer between the surface-area-and mass-distribution condensation schemes, both with the base biogenic SOA only, yielded a global increase of 8% but exceeds 100% in biogenically active regions. The percent change in N40 within the continental boundary layer between the base simulation (19 Tg yr(-1)) and the additional SOA (100 Tg yr(-1)) both using the surface area condensation scheme (very low volatility) yielded a global increase of 14%, and a global decrease in the number of particles of size D-p > 10 nm (N10) of 32%. These model simulations were compared to measured data from Hyytiala, Finland and other global locations and confirmed a decrease in the model-measurement bias. Thus, treating SOA as very low volatile as well as including additional SOA correlated with anthropogenic CO emissions causes a significant global increase in the number of climatically relevant sized particles, and therefore we must continue to refine our SOA treatments in aerosol microphysics models.
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| 3. |
- Julin, Jan, et al.
(författare)
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Molecular Dynamics Simulations of Mass Accommodation and Evaporation on Surfaces of Atmospheric Interest
- 2013
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Ingår i: NUCLEATION AND ATMOSPHERIC AEROSOLS. - : American Institute of Physics (AIP). - 9780735411524 ; , s. 437-440
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Konferensbidrag (refereegranskat)abstract
- The mass accommodation of condensable gaseous species on to the surfaces of atmospheric aerosols controls the growth of submicron-sized particles to atmospherically relevant sizes. In this work we present results from molecular dynamics simulations of mass accommodation of water and organic molecules on surfaces consisting of the same molecular species.
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| 4. |
- Keskinen, H., et al.
(författare)
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Evolution of Nanoparticle Composition in CLOUD in Presence of Sulphuric Acid, Ammonia and Organics
- 2013
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Ingår i: NUCLEATION AND ATMOSPHERIC AEROSOLS. - : American Institute of Physics (AIP). - 9780735411524 ; , s. 291-294
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Konferensbidrag (refereegranskat)abstract
- In this study, we investigate the composition of nucleated nanoparticles formed from sulphuric acid, ammonia, amines, and oxidised organics in the CLOUD chamber experiments at CERN. The investigation is carried out via analysis of the particle hygroscopicity (size range of 15-63 nm), ethanol affinity (15-50nm), oxidation state (<50 nm), and ion composition (few nanometers). The organic volume fraction of particles increased with an increase in particle diameter in presence of the sulphuric acid, ammonia and organics. Vice versa, the sulphuric acid volume fraction decreased when the particle diameter increased. The results provide information on the size-dependent composition of nucleated aerosol particles.
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| 5. |
- Kyro, Ella-Maria, et al.
(författare)
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Long-term Aerosol and Trace Gas Measurements in Eastern Lapland, Finland : The Impact of Kola Air Pollution to New Particle Formation
- 2013
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Ingår i: NUCLEATION AND ATMOSPHERIC AEROSOLS. - : American Institute of Physics (AIP). - 9780735411524 ; , s. 409-412
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Konferensbidrag (refereegranskat)abstract
- Sulfur emissions from the Kola Peninsula smelter industry have been decreasing over the past two decades. We investigated the effect of this to new particle formation at SMEAR I station in Eastern Lapland, Finland, using long-term measurements of trace gases and aerosol size distributions. We show that the number of events per year has decreased and can be linked with the decreasing sulfur emissions from Kola.
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| 6. |
- Lehtipalo, Katrianne, et al.
(författare)
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How Do Amines Affect the Growth of Recently Formed Aerosol Particles
- 2013
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Ingår i: NUCLEATION AND ATMOSPHERIC AEROSOLS. - : American Institute of Physics (AIP). - 9780735411524 ; , s. 295-297
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Konferensbidrag (refereegranskat)abstract
- Growth rates of recently born nanometer-scale particles were measured during the CLOUD experiments at CERN. Combining the data from several recently developed measurement techniques allowed us to follow the growth of the particles starting from molecules to molecular clusters and finally to climatically relevant particles. We studied the binary system with sulphuric acid and water, and the ternary systems with ammonia or dimethylamine added to the chamber, both in purely neutral situation, and with ionization from cosmic rays or the CERN particle beam.
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| 7. |
- Matisans, Modris, et al.
(författare)
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New Aerosol Particle Formation in Amazonia
- 2013
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Ingår i: NUCLEATION AND ATMOSPHERIC AEROSOLS. - : American Institute of Physics (AIP). - 9780735411524 ; , s. 571-574
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Konferensbidrag (refereegranskat)abstract
- Particle nucleation in Amazonia has been an enigma throughout decades of active scrutiny of natural nucleation processes; however, measurements have so far been thought to fail capturing an actual new particle formation (NPF) event. In this study we have analyzed latest measurements of ultra-fine particle size distributions alongside with air ion spectra and revealed a diurnal pattern of ultra-fine particle apparent growth. The revealed growth pattern is preceded by diurnal precipitation probability maxima, and simultaneous abundant ion production as detected by Neutral cluster and Air Ion Spectrometer (NAIS) data. Thus, we claim that by implementing statistical analysis of scanning mobility particle sizer (SMPS) data and combining with independent observations from Neutral cluster and Air Ion Spectrometer (NAIS) we can observe a consistent signal of NPF events in Amazonia.
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| 8. |
- Rastak, Narges, et al.
(författare)
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Modeling Aerosol Water Uptake in The Arctic Based on The kappa-Kohler Theory
- 2013
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Ingår i: Nucleation and Atmospheric Aerosols. - : American Institute of Physics (AIP). - 9780735411524 ; , s. 702-705
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Konferensbidrag (refereegranskat)abstract
- Water uptake or hygroscopicity is one of the most fundamental properties of atmospheric aerosols. Aerosol particles containing soluble materials can grow in size by absorbing water in ambient atmosphere. This property is measured by a parameter known as growth factor (GF), which is defined as the ratio of the wet diameter to the dry diameter. Hygroscopicity controls the size of an aerosol particle and therefore its optical properties in the atmosphere. Hygroscopic growth depends on the dry size of the particle, its chemical composition and the relative humidity in the ambient air (Fitzgerald, 1975; Pilinis et al., 1995). One of the typical problems in aerosol studies is the lack of measurements of aerosol size distributions and optical properties in ambient conditions. The gap between dry measurements and the real humid atmosphere is filled in this study by utilizing a hygroscopic model which calculates the hygroscopic growth of aerosol particles at Mt Zeppelin station, Ny Alesund, Svalbard during 2008.
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| 9. |
- Väänänen, Riikka, et al.
(författare)
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Analysis of particle size distribution changes between three measurement sites in Northern Scandinavia
- 2013
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Ingår i: Nucleation and Atmospheric Aerosols - 19th International Conference. - : AIP. - 1551-7616 .- 0094-243X. - 9780735411524 ; 1527, s. 531-534
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Konferensbidrag (refereegranskat)abstract
- Measured aerosol size distributions from three measurement stations and modeled air mass trajectory data were combined to study aerosol dynamics in the boreal forest zone in Northern Scandinavia. Three approaches were used: investigation of new particle formation events, analysis of air masses arriving from ocean to continent, and study of changes in the aerosol size distributions when air masses travel from one measurement site to another. The statistical analysis of air masses travelling either from the Atlantic Ocean to measurement sites or from one site to another showed that on average the condensational growth was present during the summer season, and it was not restricted only to the days when evident new particle formation was observed. The rate of this average apparent growth of particle diameter was 3-7 times smaller than the growth rate of nucleation mode particles during the new particle formation events.
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| 10. |
- Yli-Juuti, Taina, et al.
(författare)
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Effect Of Salt Formation On Condensation Of Organic Compounds On Atmospheric Nanoparticles
- 2013
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Ingår i: NUCLEATION AND ATMOSPHERIC AEROSOLS. - : AIP. - 9780735411524 ; , s. 445-448
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Konferensbidrag (refereegranskat)abstract
- Freshly formed atmospheric nanoparticles have been observed to contain also such organic compounds which have too high saturation vapor pressure to condense on nanoparticles reversibly. The condensation of these compounds on the particles may be facilitated by particle phase processes that transform the compounds into less-volatile form. Here we use particle growth model MABNAG to study the effect of particle phase acid-base chemistry on the condensation of organic acids and bases.
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