scholarly journals Relative importance of gas uptake on aerosol and ground surfaces characterized by equivalent uptake coefficients

2019 ◽  
Vol 19 (16) ◽  
pp. 10981-11011 ◽  
Author(s):  
Meng Li ◽  
Hang Su ◽  
Guo Li ◽  
Nan Ma ◽  
Ulrich Pöschl ◽  
...  

Abstract. Quantifying the relative importance of gas uptake on the ground and aerosol surfaces helps to determine which processes should be included in atmospheric chemistry models. Gas uptake by aerosols is often characterized by an effective uptake coefficient (γeff), whereas gas uptake on the ground is usually described by a deposition velocity (Vd). For efficient comparison, we introduce an equivalent uptake coefficient (γeqv) at which the uptake flux of aerosols would equal that on the ground surface. If γeff is similar to or larger than γeqv, aerosol uptake is important and should be included in atmospheric models. In this study, we compare uptake fluxes in the planetary boundary layer (PBL) for different reactive trace gases (O3, NO2, SO2, N2O5, HNO3 and H2O2), aerosol types (mineral dust, soot, organic aerosol and sea salt aerosol), environments (urban areas, agricultural land, the Amazon forest and water bodies), seasons and mixing heights. For all investigated gases, γeqv ranges from magnitudes of 10−6–10−4 in polluted urban environments to 10−4–10−1 under pristine forest conditions. In urban areas, aerosol uptake is relevant for all species (γeff≥γeqv) and should be considered in models. On the contrary, contributions of aerosol uptakes in the Amazon forest are minor compared with the dry deposition. The phase state of aerosols could be one of the crucial factors influencing the uptake rates. Current models tend to underestimate the O3 uptake on liquid organic aerosols which can be important, especially over regions with γeff≥γeqv. H2O2 uptakes on a variety of aerosols are yet to be measured under laboratory conditions and evaluated. Given the fact that most models have considered the uptakes of these species on the ground surface, we suggest also considering the following processes in atmospheric models: N2O5 uptake by all types of aerosols, HNO3 and SO2 uptake by mineral dust and sea salt aerosols, H2O2 uptake by mineral dust, NO2 uptakes by sea salt aerosols and O3 uptake by liquid organic aerosols.

2019 ◽  
Author(s):  
Meng Li ◽  
Hang Su ◽  
Guo Li ◽  
Nan Ma ◽  
Ulrich Pöschl ◽  
...  

Abstract. Quantifying the relative importance of gas uptake on the ground and aerosol surfaces helps to determine which processes should be included in atmospheric chemistry models. Gas uptake by aerosols is often characterized by an effective uptake coefficient (γeff), whereas gas uptake on the ground is usually described by a deposition velocity (Vd). For efficient comparison, we introduce an equivalent uptake coefficient (γeqv) at which the uptake flux of aerosols would equal that on the ground surface. If γeff is similar to or larger than γeqv, aerosol uptake is important and should be included in atmospheric models. In this study, we compare uptake fluxes in the planetary boundary layer (PBL) for different reactive trace gases (O3, NO2, SO2, N2O5, HNO3, H2O2), aerosol types (mineral dust, soot, organic aerosol, sea salt aerosol), environments (urban, agricultural land, Amazon forest, water body), seasons, and mixing heights. For all investigated gases, γeqv ranges from 10−6 ~ 10−4 in polluted urban environments to 10−4 ~ 10−1 under pristine forest conditions. In urban areas, aerosol uptake is relevant for all species (γeff ≥ γeqv) and should be considered in models. On the contrary, contributions of aerosol uptakes in Amazon forest are minor compared to the dry deposition. Phase state of aerosols could be one of the crucial factors influencing the uptake rates. Current models tend to underestimate the O3 uptake on liquid organic aerosols which can be important especially over regions with γeff ≥ γeqv. H2O2 uptakes on a variety of aerosols is yet to be measured at laboratory and evaluated. Given the fact that most models have considered their uptakes on the ground surface, we suggest also considering the N2O5 uptake by all types of aerosols, HNO3 and H2O2 uptakes by mineral dust, O3 uptake by liquid organic aerosols and NO2, SO2, HNO3 uptakes by sea salt aerosols in atmospheric models.


2007 ◽  
Vol 41 (2) ◽  
pp. 136-159 ◽  
Author(s):  
Cameron S. McNaughton ◽  
Antony D. Clarke ◽  
Steven G. Howell ◽  
Mitchell Pinkerton ◽  
Bruce Anderson ◽  
...  

2019 ◽  
Vol 19 (4) ◽  
pp. 2115-2133 ◽  
Author(s):  
Liya Guo ◽  
Wenjun Gu ◽  
Chao Peng ◽  
Weigang Wang ◽  
Yong Jie Li ◽  
...  

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.


2018 ◽  
Author(s):  
Liya Guo ◽  
Wenjun Gu ◽  
Chao Peng ◽  
Weigang Wang ◽  
Yong Jie Li ◽  
...  

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.


Author(s):  
Yeny A. Tobon ◽  
Danielle El Hajj ◽  
Samantha Seng ◽  
Ferdaous Bengrad ◽  
Myriam Moreau ◽  
...  

Sodium chloride (NaCl) is the main constituent of sea-salt aerosols. During atmospheric transport, sea-salt aerosols can interact with gases and other particles including secondary aerosols containing ammonium sulfate ((NH4)2SO4). This...


2010 ◽  
Vol 10 (6) ◽  
pp. 2965-2974 ◽  
Author(s):  
M. J. Tang ◽  
J. Thieser ◽  
G. Schuster ◽  
J. N. Crowley

Abstract. The uptake of NO3 and N2O5 to Saharan dust, ambient aerosols and soot was investigated using a novel and simple relative rate method with simultaneous detection of both NO3 and N2O5. The use of cavity ring down spectroscopy to detect both trace gases enabled the measurements to be carried out at low mixing ratios (<500 pptv or 1×1010 molecule cm−3). The uptake coefficient ratio, γ(NO3)/γ(N2O5), was determined to be 0.9±0.4 for Saharan dust, independent of relative humidity, NO3 or N2O5 mixing ratio and exposure time. Ambient (urban) aerosols showed a very limited capacity to take up N2O5 but were reactive towards NO3 with γ(NO3)/γ(N2O5)>15. A value of γ(NO3)/γ(N2O5)~1.5–3 was obtained when using candle generated soot. The relative rate obtained for Saharan dust can be placed on an absolute basis using our recently determined value of γ(N2O5)=1×10−2 to give γ(NO3)=9×10−3, which is significantly smaller than the single previous value. With the present uptake coefficient, reaction of NO3 with mineral dust will generally not contribute significantly to its NO3 loss in the boundary atmosphere or to the nitration of mineral dust.


2021 ◽  
Vol 87 (4) ◽  
pp. 237-248
Author(s):  
Nahed Osama ◽  
Bisheng Yang ◽  
Yue Ma ◽  
Mohamed Freeshah

The ICE, Cloud and land Elevation Satellite-2 (ICES at-2) can provide new measurements of the Earth's elevations through photon-counting technology. Most research has focused on extracting the ground and the canopy photons in vegetated areas. Yet the extraction of the ground photons from urban areas, where the vegetation is mixed with artificial constructions, has not been fully investigated. This article proposes a new method to estimate the ground surface elevations in urban areas. The ICES at-2 signal photons were detected by the improved Density-Based Spatial Clustering of Applications with Noise algorithm and the Advanced Topographic Laser Altimeter System algorithm. The Advanced Land Observing Satellite-1 PALSAR –derived digital surface model has been utilized to separate the terrain surface from the ICES at-2 data. A set of ground-truth data was used to evaluate the accuracy of these two methods, and the achieved accuracy was up to 2.7 cm, which makes our method effective and accurate in determining the ground elevation in urban scenes.


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