scholarly journals A comprehensive study of hygroscopic properties of calcium- and magnesium-containing salts: implication for hygroscopicity of mineral dust and sea salt aerosols

2018 ◽  
Author(s):  
Liya Guo ◽  
Wenjun Gu ◽  
Chao Peng ◽  
Weigang Wang ◽  
Yong Jie Li ◽  
...  
Keyword(s):  
Growth Factors ◽  
Physicochemical Properties ◽  
Mineral Dust ◽  
Aerosol Particles ◽  
Sea Salt ◽  
Hygroscopic Growth ◽  
Continuous Growth ◽  
Sea Salt Aerosols ◽  
Hygroscopic Properties ◽  
Calcium And Magnesium

Abstract. Calcium- and magnesium-containing salts are important components for mineral dust and sea salt aerosols, but their physicochemical properties are not well understood yet. In this study, the hygroscopic properties of eight Ca- and Mg-containing salts, including Ca(NO3)2 · 4H2O, Mg(NO3)2 · 6H2O, MgCl2 · 6H2O, CaCl2 · 6H2O, Ca(HCOO)2, Mg(HCOO)2 · 2H2O, Ca(CH3COO)2 · H2O and Mg(CH3COO)2 · 4H2O, were systematically investigated using two complementary techniques. A vapor sorption analyzer was used to measure the change of sample mass with relative humidity (RH) under isotherm conditions, and the deliquescence relative humidities (DRH) for temperature in the range of 5–30 °C as well as water-to-solute ratios as a function of RH at 5 and 25 °C were reported for these eight compounds. DRH values showed a large variation for these compounds; for example, at 25 °C the DRH values were measured to be ~ 28.5 % for CaCl2 · 6H2O and > 95 % for Ca(HCOO)2 and Mg(HCOO)2 · 2H2O. In addition, a humidity-tandem differential analyzer was used to measure the change in mobility diameter with RH (up to 90 %) at room temperature, in order to determine the hygroscopic growth factors of aerosol particles generated by atomizing water solutions of these eight compounds. All the aerosol particles studied in this work, very likely to be amorphous, started to grow at very low RH (as low as 10 %) and showed continuous growth with RH. The hygroscopic growth factors at 90 % RH were found to range from 1.26 ± 0.04 for Ca(HCOO2)2 and 1.79 ± 0.03 for Ca(NO3)2, varying significantly for the eight types of aerosols considered herein. Overall, our work provides a systematical and comprehensive investigation of the hygroscopic properties of these Ca- and Mg-containing salts, largely improving our knowledge in the physicochemical properties of mineral dust and sea salt aerosols.

scholarly journals A comprehensive study of hygroscopic properties of calcium- and magnesium-containing salts: implication for hygroscopicity of mineral dust and sea salt aerosols

2019 ◽  
Vol 19 (4) ◽  
pp. 2115-2133 ◽  
Author(s):  
Liya Guo ◽  
Wenjun Gu ◽  
Chao Peng ◽  
Weigang Wang ◽  
Yong Jie Li ◽  
...  
Keyword(s):  
Growth Factors ◽  
Physicochemical Properties ◽  
Mineral Dust ◽  
Aerosol Particles ◽  
Sea Salt ◽  
Hygroscopic Growth ◽  
Continuous Growth ◽  
Sea Salt Aerosols ◽  
Hygroscopic Properties ◽  
Calcium And Magnesium

Abstract. Calcium- and magnesium-containing salts are important components for mineral dust and sea salt aerosols, but their physicochemical properties are not well understood yet. In this study, hygroscopic properties of eight Ca- and Mg-containing salts, including Ca(NO3)2⚫4H2O, Mg(NO3)2⚫6H2O, MgCl2⚫6H2O, CaCl2⚫6H2O, Ca(HCOO)2, Mg(HCOO)2⚫2H2O, Ca(CH3COO)2⚫H2O and Mg(CH3COO)2⚫4H2O, were investigated using two complementary techniques. A vapor sorption analyzer was used to measure the change of sample mass with relative humidity (RH) under isotherm conditions, and the deliquescence relative humidities (DRHs) for temperature in the range of 5–30 ∘C as well as water-to-solute ratios as a function of RH at 5 and 25 ∘C were reported for these eight compounds. DRH values showed large variation for these compounds; for example, at 25 ∘C DRHs were measured to be ∼ 28.5 % for CaCl2⚫6H2O and >95 % for Ca(HCOO)2 and Mg(HCOO)2⚫2H2O. We further found that the dependence of DRH on temperature can be approximated by the Clausius–Clapeyron equation. In addition, a humidity tandem differential mobility analyzer was used to measure the change in mobility diameter with RH (up to 90 %) at room temperature, in order to determine hygroscopic growth factors of aerosol particles generated by atomizing water solutions of these eight compounds. All the aerosol particles studied in this work, very likely to be amorphous under dry conditions, started to grow at very low RH (as low as 10 %) and showed continuous growth with RH. Hygroscopic growth factors at 90 % RH were found to range from 1.26 ± 0.04 for Ca(HCOO)2 to 1.79 ± 0.03 for Ca(NO3)2, and the single hygroscopicity parameter ranged from 0.09–0.13 for Ca(CH3COO)2 to 0.49–0.56 for Ca(NO3)2. Overall, our work provides a comprehensive investigation of hygroscopic properties of these Ca- and Mg-containing salts, largely improving our knowledge of the physicochemical properties of mineral dust and sea salt aerosols.

scholarly journals Hygroscopic properties of ultrafine aerosol particles in the boreal forest: diurnal variation, solubility and the influence of sulfuric acid

2007 ◽  
Vol 7 (1) ◽  
pp. 211-222 ◽  
Author(s):  
M. Ehn ◽  
T. Petäjä ◽  
H. Aufmhoff ◽  
P. Aalto ◽  
K. Hämeri ◽  
...  
Keyword(s):  
Sulfuric Acid ◽  
Boreal Forest ◽  
Diurnal Variation ◽  
Gas Phase ◽  
Aerosol Particles ◽  
Particle Formation ◽  
Time Of Day ◽  
New Particle Formation ◽  
Hygroscopic Growth ◽  
Hygroscopic Properties

Abstract. The hygroscopic growth of aerosol particles present in a boreal forest was measured at a relative humidity of 88%. Simultaneously the gas phase concentration of sulfuric acid, a very hygroscopic compound, was monitored. The focus was mainly on days with new particle formation by nucleation. The measured hygroscopic growth factors (GF) correlated positively with the gaseous phase sulfuric acid concentrations. The smaller the particles, the stronger the correlation, with r=0.20 for 50 nm and r=0.50 for 10 nm particles. The increase in GF due to condensing sulfuric acid is expected to be larger for particles with initially smaller masses. During new particle formation, the changes in solubility of the new particles were calculated during their growth to Aitken mode sizes. As the modal diameter increased, the solubility of the particles decreased. This indicated that the initial particle growth was due to more hygroscopic compounds, whereas the later growth during the evening and night was mainly caused by less hygroscopic or even hydrophobic compounds. For all the measured sizes, a diurnal variation in GF was observed both during days with and without particle formation. The GF was lowest at around midnight, with a mean value of 1.12–1.24 depending on particle size and if new particle formation occurred during the day, and increased to 1.25–1.34 around noon. This can be tentatively explained by day- and nighttime gas-phase chemistry; different vapors will be present depending on the time of day, and through condensation these compounds will alter the hygroscopic properties of the particles in different ways.

scholarly journals Results from the DC-8 Inlet Characterization Experiment (DICE): Airborne Versus Surface Sampling of Mineral Dust and Sea Salt Aerosols

2007 ◽  
Vol 41 (2) ◽  
pp. 136-159 ◽  
Author(s):  
Cameron S. McNaughton ◽  
Antony D. Clarke ◽  
Steven G. Howell ◽  
Mitchell Pinkerton ◽  
Bruce Anderson ◽  
...  
Keyword(s):  
Mineral Dust ◽  
Sea Salt ◽  
Surface Sampling ◽  
Sea Salt Aerosols

scholarly journals Hygroscopicity of Different Types of Aerosol Particles: Case Studies Using Multi-Instrument Data in Megacity Beijing, China

2020 ◽  
Vol 12 (5) ◽  
pp. 785 ◽  
Author(s):  
Tong Wu ◽  
Zhanqing Li ◽  
Jun Chen ◽  
Yuying Wang ◽  
Hao Wu ◽  
...  
Keyword(s):  
Enhancement Factor ◽  
Mineral Dust ◽  
Aerosol Particles ◽  
Dust Aerosol ◽  
Dust Particles ◽  
Chemical Components ◽  
Hygroscopic Growth ◽  
Microphysical Properties ◽  
Fine Mode ◽  
Fine Mode Aerosol

Water uptake by aerosol particles alters its light-scattering characteristics significantly. However, the hygroscopicities of different aerosol particles are not the same due to their different chemical and physical properties. Such differences are explored by making use of extensive measurements concerning aerosol optical and microphysical properties made during a field experiment from December 2018 to March 2019 in Beijing. The aerosol hygroscopic growth was captured by the aerosol optical characteristics obtained from micropulse lidar, aerosol chemical composition, and aerosol particle size distribution information from ground monitoring, together with conventional meteorological measurements. Aerosol hygroscopicity behaves rather distinctly for mineral dust coarse-mode aerosol (Case I) and non-dust fine-mode aerosol (Case II) in terms of the hygroscopic enhancement factor, f β ( R H , λ 532 ) , calculated for the same humidity range. The two types of aerosols were identified by applying the polarization lidar photometer networking method (POLIPHON). The hygroscopicity for non-dust aerosol was much higher than that for dust conditions with the f β ( R H , λ 532 ) being around 1.4 and 3.1, respectively, at the relative humidity of 86% for the two cases identified in this study. To study the effect of dust particles on the hygroscopicity of the overall atmospheric aerosol, the two types of aerosols were identified and separated by applying the polarization lidar photometer networking method in Case I. The hygroscopic enhancement factor of separated non-dust fine-mode particles in Case I had been significantly strengthened, getting closer to that of the total aerosol in Case II. These results were verified by the hygroscopicity parameter, κ (Case I non-dust particles: 0.357 ± 0.024; Case II total: 0.344 ± 0.026), based on the chemical components obtained by an aerosol chemical speciation instrument, both of which showed strong hygroscopicity. It was found that non-dust fine-mode aerosol contributes more during hygroscopic growth and that non-hygroscopic mineral dust aerosol may reduce the total hygroscopicity per unit volume in Beijing.

scholarly journals Tandem configuration of differential mobility and centrifugal particle mass analysers for investigating aerosol hygroscopic properties

2017 ◽  
Vol 10 (3) ◽  
pp. 1269-1280 ◽  
Author(s):  
Sergey S. Vlasenko ◽  
Hang Su ◽  
Ulrich Pöschl ◽  
Meinrat O. Andreae ◽  
Eugene F. Mikhailov
Keyword(s):  
Water Uptake ◽  
Aerosol Particles ◽  
Interaction Model ◽  
Growth Curves ◽  
Particle Mass ◽  
Submicron Particles ◽  
Hygroscopic Growth ◽  
Differential Mobility ◽  
Hygroscopic Properties ◽  
Modal Mass

Abstract. A tandem arrangement of Differential Mobility Analyser and Humidified Centrifugal Particle Mass Analyser (DMA-HCPMA) was developed to measure the deliquescence and efflorescence thresholds and the water uptake of submicron particles over the relative humidity (RH) range from 10 to 95 %. The hygroscopic growth curves obtained for ammonium sulfate and sodium chloride test aerosols are consistent with thermodynamic model predictions and literature data. The DMA-HCPMA system was applied to measure the hygroscopic properties of urban aerosol particles, and the kappa mass interaction model (KIM) was used to characterize and parameterize the concentration-dependent water uptake observed in the 50–95 % RH range. For DMA-selected 160 nm dry particles (modal mass of 3.5 fg), we obtained a volume-based hygroscopicity parameter, κv ≈  0.2, which is consistent with literature data for freshly emitted urban aerosols.Overall, our results show that the DMA-HCPMA system can be used to measure size-resolved mass growth factors of atmospheric aerosol particles upon hydration and dehydration up to 95 % RH. Direct measurements of particle mass avoid the typical complications associated with the commonly used mobility-diameter-based HTDMA technique (mainly due to poorly defined or unknown morphology and density).

scholarly journals Mixing states of Amazon-basin aerosol particles transported over long distances using transmission electron microscopy

2020 ◽  
Author(s):  
Kouji Adachi ◽  
Naga Oshima ◽  
Zhaoheng Gong ◽  
Suzane de Sá ◽  
Adam P. Bateman ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Amazon Basin ◽  
Mineral Dust ◽  
Aerosol Particles ◽  
Sea Salt ◽  
Anthropogenic Sources ◽  
Natural Sources ◽  
Transmission Electron ◽  
Mixing States

Abstract. The Amazon basin is important for understanding the global climate both because of its carbon cycle and as a laboratory for obtaining basic knowledge of the continental background atmosphere. Aerosol particles play an important role in the climate and weather, and knowledge of their compositions and mixing states is necessary to understand their influence on the climate. For this study, we collected aerosol particles from the Amazon basin during the Green Ocean Amazon (GoAmazon2014/5) campaign (February to March 2014) at the T3 site, which locates about 70 km from Manaus, and analyzed using transmission electron microscopy (TEM). TEM has better spatial resolution than other instruments, which enables us to analyse the occurrences of components that attach to or are embedded within other particles. Based on the TEM results of more than 10,000 particles from several transport events, this study shows the occurrences of individual particles including compositions, size distributions, number fractions, and possible sources of materials that mix with other particles. Aerosol particles during the wet season were from both natural sources such as the Amazon forest, Saharan desert, Atlantic Ocean, and African biomass burning and anthropogenic sources such as Manaus and local emissions. These particles mix together at an individual particle scale. The number fractions of mineral dust and sea-salt particles increased almost three-fold when long-range transport (LRT) from the African continent occurred. Nearly 20 % of mineral dust and primary biological aerosol particles attached sea salts on their surfaces. Sulfates were also internally mixed with sea-salt and mineral dust particles. The TEM element mapping images showed that several components with sizes of hundreds of nanometres from different sources commonly occur within individual LRT aerosol particles. We conclude that many aerosol particles from natural sources change their compositions by mixing during transport. The compositions and mixing states of these particles after emission result in changes in their hygroscopic and optical properties and should be considered when assessing their effects on climate.

scholarly journals Characterisation of individual aerosol particles collected during a haze episode in Incheon, Korea using the quantitative ED-EPMA technique

2011 ◽  
Vol 11 (3) ◽  
pp. 1327-1337 ◽  
Author(s):  
H. Geng ◽  
J. Y. Ryu ◽  
S. Maskey ◽  
H.-J. Jung ◽  
C.-U. Ro
Keyword(s):  
Mineral Dust ◽  
Aerosol Particles ◽  
Relative Number ◽  
Sea Salt ◽  
Motor Vehicles ◽  
Dust Particles ◽  
Formation Mechanisms ◽  
X Ray ◽  
Haze Episode ◽  
Haze Days

Abstract. A quantitative energy-dispersive electron probe X-ray microanalysis (ED-EPMA), called low-Z particle EPMA, was used to analyse individual aerosol particles collected in Incheon, Korea on 13–18 October 2008 (a typical haze episode occurred from 15 to 18 October). Overall 3600 individual particles in PM2.5-10 and PM1.0-2.5 fractions from 12 aerosol samples collected on haze and non-haze days were analysed. The analysed particles were classified, based on their X-ray spectral data together with their secondary electron images. The major particle types included organic carbon (OC), elemental carbon (EC), sea-salt, mineral dust (such as aluminosilicate, SiO2, CaCO3/CaMgCO3, etc.), (NH4)2SO4/NH4HSO4-containing, K-containing, Fe-rich and fly ash particles. Their relative number abundance results showed that OC particles were significantly increased while sea-salts and mineral dust particles were significantly decreased (especially in PM1.0-2.5 fraction) when haze occurred. For the other particle types (except Fe-rich particles in PM2.5-10 fraction), there were no significant differences in their relative abundances between haze and non-haze samples. On non-haze days, the nitrate-containing reacted sea-salt and mineral dust particles in PM1.0-2.5 fraction significantly outnumbered the sulfate-containing ones, whereas it was the reverse on haze days, implying that on haze days there were special sources or formation mechanisms for fine aerosol particles (≤2.5 μm in aerodynamic diameter). The emission of air pollutants from motor vehicles and stagnant meteorological conditions, such as low wind speed and high relative humidity, might be responsible for the elevated level of OC particles on haze days.

scholarly journals Chemical composition, microstructure, and hygroscopic properties of aerosol particles at the Zotino Tall Tower Observatory (ZOTTO), Siberia, during a summer campaign

2015 ◽  
Vol 15 (15) ◽  
pp. 8847-8869 ◽  
Author(s):  
E. F. Mikhailov ◽  
G. N. Mironov ◽  
C. Pöhlker ◽  
X. Chi ◽  
M. L. Krüger ◽  
...  
Keyword(s):  
Organic Carbon ◽  
Water Uptake ◽  
Aerosol Particles ◽  
Organic Coating ◽  
Water Soluble ◽  
Submicron Particles ◽  
Hygroscopic Growth ◽  
Accumulation Mode ◽  
Hygroscopic Properties ◽  
Coarse Mode

Abstract. In this study we describe the hygroscopic properties of accumulation- and coarse-mode aerosol particles sampled at the Zotino Tall Tower Observatory (ZOTTO) in central Siberia (61° N, 89° E) from 16 to 21 June 2013. The hygroscopic growth measurements were supplemented with chemical analyses of the samples, including inorganic ions and organic/elemental carbon. In addition, the microstructure and chemical compositions of aerosol particles were analyzed by x-ray micro-spectroscopy (STXM-NEXAFS) and transmission electron microscopy (TEM). A mass closure analysis indicates that organic carbon accounted for 61 and 38 % of particulate matter (PM) in the accumulation mode and coarse mode, respectively. The water-soluble fraction of organic matter was estimated to be 52 and 8 % of PM in these modes. Sulfate, predominantly in the form of ammoniated sulfate, was the dominant inorganic component in both size modes: ~ 34 % in the accumulation mode vs. ~ 47 % in the coarse mode. The hygroscopic growth measurements were conducted with a filter-based differential hygroscopicity analyzer (FDHA) over the range of 5–99.4 % RH in the hydration and dehydration operation modes. The FDHA study indicates that both accumulation and coarse modes exhibit pronounced water uptake approximately at the same relative humidity (RH), starting at ~ 70 %, while efflorescence occurred at different humidities, i.e., at ~ 35 % RH for submicron particles vs. ~ 50 % RH for supermicron particles. This ~ 15 % RH difference was attributed to higher content of organic material in the submicron particles, which suppresses water release in the dehydration experiments. The kappa mass interaction model (KIM) was applied to characterize and parameterize non-ideal solution behavior and concentration-dependent water uptake by atmospheric aerosol samples in the 5–99.4 % RH range. Based on KIM, the volume-based hygroscopicity parameter, κv, was calculated. The κv,ws value related to the water-soluble (ws) fraction was estimated to be ~ 0.15 for the accumulation mode and ~ 0.36 for the coarse mode, respectively. The obtained κv,ws for the accumulation mode is in good agreement with earlier data reported for remote sites in the Amazon rain forest (κv ≈ 0.15) and a Colorado mountain forest (κv ≈ 0.16 ). We used the Zdanovskii–Stokes–Robinson (ZSR) mixing rule to predict the chemical composition dependent hygroscopicity, κv,p. The obtained κv,p values overestimate the experimental FDHA-KIM-derived κv,ws by factors of 1.8 and 1.5 for the accumulation and coarse modes, respectively. This divergence can be explained by incomplete dissolution of the hygroscopic inorganic compounds resulting from kinetic limitations due to a sparingly soluble organic coating. The TEM and STXM-NEXAFS results indicate that aged submicron (> 300 nm) and supermicron aerosol particles possess core–shell structures with an inorganic core, and are enriched in organic carbon at the mixed particle surface. The direct FDHA kinetic studies provide a bulk diffusion coefficient of water of ~ 10−12 cm2 s−1 indicating a semi-solid state of the organic-rich phase leading to kinetic limitations of water uptake and release during hydration and dehydration cycles. Overall, the present ZOTTO data set, obtained in the growing season, has revealed a strong influence of organic carbon on the hygroscopic properties of the ambient aerosols. The sparingly soluble organic coating controls hygroscopic growth, phase transitions, and microstructural rearrangement processes. The observed kinetic limitations can strongly influence the outcome of experiments performed on multi-second timescales, such as the commonly applied HTDMA (Hygroscopicity Tandem Differential Mobility Analyzer) and CCNC (Cloud Condensation Nuclei Counter) measurements.

scholarly journals Tandem configuration of differential mobility and centrifugal particle mass analyzers for investigating aerosol hygroscopic properties

2016 ◽  
Author(s):  
Sergey S. Vlasenko ◽  
Hang Su ◽  
Ulrich Pöschl ◽  
Meinrat O. Andreae ◽  
Eugene F. Mikhailov
Keyword(s):  
Water Uptake ◽  
Aerosol Particles ◽  
Interaction Model ◽  
Particle Morphology ◽  
Particle Mass ◽  
Submicron Particles ◽  
Mass Analyzer ◽  
Hygroscopic Growth ◽  
Differential Mobility ◽  
Hygroscopic Properties

Abstract. A tandem arrangement of Differential Mobility Analyzer and Humidified Centrifugal Particle Mass Analyzer (DMA-HCPMA) was developed to measure the deliquescence and efflorescence thresholds and the water uptake of submicron particles over the relative humidity (RH) range from 10 % to 95 %. The hygroscopic growth curves obtained for Ammonium sulfate and sodium chloride test aerosols are consistent with thermodynamic model predictions and literature data. The DMA-HCPMA system was applied to measure the hygroscopic properties of urban aerosol particles, and the kappa mass interaction model (KIM) was used to characterize and parameterize the concentration-dependent water uptake observed in the 50–95 % RH range. For DMA-selected 160 nm dry particles (mass of 3.5 fg), we obtained a volume-based hygroscopicity parameter κv ≈ 0.2, which is consistent with literature data for freshly emitted urban aerosols. Overall, our results show that the DMA-HCPMA system can be used to measure size-resolved mass growth factors of atmospheric aerosol particles upon hydration and dehydration up to 95 % RH. The direct measurements of humidified particle mass allow avoiding complications that occur in the commonly used mobility-diameter-based HTDMA technique due to poorly defined particle morphology and density.

scholarly journals Chemical composition and hygroscopic properties of aerosol particles over the Aegean Sea

2013 ◽  
Vol 13 (3) ◽  
pp. 5805-5841 ◽  
Author(s):  
S. Bezantakos ◽  
K. Barmpounis ◽  
M. Giamarelou ◽  
E. Bossioli ◽  
M. Tombrou ◽  
...  
Keyword(s):  
Growth Factors ◽  
Chemical Composition ◽  
Volume Fraction ◽  
Aegean Sea ◽  
Average Density ◽  
Back Trajectory ◽  
High Time Resolution ◽  
Hygroscopic Growth ◽  
Organic Species ◽  
Hygroscopic Properties

Abstract. The chemical composition and water uptake characteristics of sub-micrometer atmospheric particles in the region of the Aegean Sea were measured between 25 August and 11 September 2011 in the framework of the Aegean-Game campaign. High time-resolution measurements of the chemical composition of the particles were conducted using an airborne compact Time-Of-Flight Aerosol Mass Spectrometer (cTOF-AMS). These measurements involved two flights from the island of Crete to the island of Lemnos and back. A Hygroscopic Tandem Differential Mobility Analyzer (HTDMA) located on the island of Lemnos was used to measure the ability of the particles to take up water. The HTDMA measurements showed that the particles were internally mixed, having hygroscopic growth factors that ranged from 1.00 to 1.59 when exposed to 85% relative humidity. When the aircraft flew near the ground station on Lemnos, the cTOF-AMS measurements showed that the organic volume fraction of the particles ranged from 43 to 56%. These measurements corroborate the range of hygroscopic growth factors measured by the HTDMA during that time. Good closure between HTDMA and cTOF-AMS measurements was achieved when assuming that the organic species were hydrophobic and had an average density that corresponds to aged organic species. Using the results from the closure study, the cTOF-AMS measurements were employed to determine a representative aerosol hygroscopic parameter κmix for the whole path of the two flights. Calculated κmix values ranged from 0.17 to 1.03 during the first flight and from 0.15 to 0.93 during the second flight. Air masses of different origin as determined by back trajectory calculations can explain the spatial variation in the chemical composition and κmix values of the particles observed in the region.

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