scholarly journals Interactive comment on “Investigation of water adsorption and hygroscopicity 1 of atmospheric particles using a commercial vapor sorption analyzer” by W. Gu et al.

2017 ◽  
Author(s):  
Anonymous
2017 ◽  
Vol 10 (10) ◽  
pp. 3821-3832 ◽  
Author(s):  
Wenjun Gu ◽  
Yongjie Li ◽  
Jianxi Zhu ◽  
Xiaohong Jia ◽  
Qinhao Lin ◽  
...  

Abstract. Water adsorption and hygroscopicity are among the most important physicochemical properties of aerosol particles, largely determining their impacts on atmospheric chemistry, radiative forcing, and climate. Measurements of water adsorption and hygroscopicity of nonspherical particles under subsaturated conditions are nontrivial because many widely used techniques require the assumption of particle sphericity. In this work we describe a method to directly quantify water adsorption and mass hygroscopic growth of atmospheric particles for temperature in the range of 5–30 °C, using a commercial vapor sorption analyzer. A detailed description of instrumental configuration and experimental procedures, including relative humidity (RH) calibration, is provided first. It is then demonstrated that for (NH4)2SO4 and NaCl, deliquescence relative humidities and mass hygroscopic growth factors measured using this method show good agreements with experimental and/or theoretical data from literature. To illustrate its ability to measure water uptake by particles with low hygroscopicity, we used this instrument to investigate water adsorption by CaSO4 ⋅ 2H2O as a function of RH at 25 °C. The mass hygroscopic growth factor of CaSO4 ⋅ 2H2O at 95 % RH, relative to that under dry conditions (RH  < 1 %), was determined to be (0.450±0.004) % (1σ). In addition, it is shown that this instrument can reliably measure a relative mass change of 0.025 %. Overall, we have demonstrated that this commercial instrument provides a simple, sensitive, and robust method to investigate water adsorption and hygroscopicity of atmospheric particles.


2017 ◽  
Author(s):  
Wenjun Gu ◽  
Yongjie Li ◽  
Jianxi Zhu ◽  
Xiaohong Jia ◽  
Qinhao Lin ◽  
...  

Abstract. Water adsorption and hygroscopicity are among the most important physicochemical properties of aerosol particles, largely determining their impacts on atmospheric chemistry, radiative forcing, and climate. Measurements of water adsorption and hygroscopicity of nonspherical particles under subsaturation conditions are non-trivial because many widely used techniques require the assumption of particle sphericity. In this work we describe a method to directly quantify water adsorption and mass hygroscopic growth of atmospheric particles for temperature in the range of 5–30 °C, using a commercial vapor sorption analyzer. A detailed description of instrumental configuration and experimental procedures, including relative humidity (RH) calibration, are provided first. It is then demonstrated that for (NH4)2SO4 and NaCl, deliquescence relative humidities (DRHs) and mass hygroscopic growth factors measured using this method show good agreements with experimental and/or theoretical data from literature. To illustrate its ability to measure water uptake by particles with low hygroscopicity, we used this instrument to investigate water adsorption by CaSO4 ∙ 2H2O as a function of RH at 25 °C. The mass hygroscopic growth factor of CaSO4 ∙ 2H2O at 95 % RH, relative to that under dry conditions (RH 


2020 ◽  
Vol 20 (21) ◽  
pp. 13611-13626
Author(s):  
Lanxiadi Chen ◽  
Chao Peng ◽  
Wenjun Gu ◽  
Hanjing Fu ◽  
Xing Jian ◽  
...  

Abstract. Despite its importance, hygroscopicity of mineral dust aerosol remains highly uncertain. In this work, we investigated water adsorption and hygroscopicity of different mineral dust samples at 25 ∘C, via measurement of sample mass at different relative humidity (RH, up to 90 %) using a vapor sorption analyzer. Mineral dust samples examined (21 in total) included seven authentic mineral dust samples from different regions in the world and 14 major minerals contained in mineral dust aerosol. At 90 % RH, the mass ratios of adsorbed water to the dry mineral ranged from 0.0011 to 0.3080, largely depending on the BET surface areas of mineral dust samples. The fractional surface coverages of adsorbed water were determined to vary between 1.26 and 8.63 at 90 % RH, and it was found that the Frenkel–Halsey–Hill (FHH) adsorption isotherm could describe surface coverages of adsorbed water as a function of RH well, with AFHH and BFHH parameters in the range of 0.15–4.39 and 1.10–1.91, respectively. The comprehensive and robust data obtained would largely improve our knowledge of hygroscopicity of mineral dust aerosol.


2021 ◽  
Author(s):  
Mingjin Tang ◽  
Lanxiadi Chen ◽  
Chao Peng ◽  
Wenjun Gu

&lt;p&gt;Despite its importance, hygroscopicity of mineral dust aerosol remains highly uncertain. In this work, we investigated water adsorption and hygroscopicity of different mineral dust samples at 25&amp;#8201;&amp;#8728;C, via measurement of sample mass at different relative humidity (RH, up to 90&amp;#8201;%) using a vapor sorption analyzer. Mineral dust samples examined (21 in total) included seven authentic mineral dust samples from different regions in the world and 14 major minerals contained in mineral dust aerosol. At 90&amp;#8201;%&amp;#8201;RH, the mass ratios of adsorbed water to the dry mineral ranged from 0.0011 to 0.3080, largely depending on the BET surface areas of mineral dust samples. The fractional surface coverages of adsorbed water were determined to vary between 1.26 and 8.63 at 90&amp;#8201;%&amp;#8201;RH, and it was found that the Frenkel&amp;#8211;Halsey&amp;#8211;Hill (FHH) adsorption isotherm could describe surface coverages of adsorbed water as a function of RH well, with AFHH and BFHH parameters in the range of 0.15&amp;#8211;4.39 and 1.10&amp;#8211;1.91, respectively. The comprehensive and robust data obtained would largely improve our knowledge of hygroscopicity of mineral dust aerosol.&lt;/p&gt;


2019 ◽  
Author(s):  
Jose Julio Gutierrez Moreno ◽  
Marco Fronzi ◽  
Pierre Lovera ◽  
alan O'Riordan ◽  
Mike J Ford ◽  
...  

<p></p><p>Interfacial metal-oxide systems with ultrathin oxide layers are of high interest for their use in catalysis. In this study, we present a density functional theory (DFT) investigation of the structure of ultrathin rutile layers (one and two TiO<sub>2</sub> layers) supported on TiN and the stability of water on these interfacial structures. The rutile layers are stabilized on the TiN surface through the formation of interfacial Ti–O bonds. Charge transfer from the TiN substrate leads to the formation of reduced Ti<sup>3+</sup> cations in TiO<sub>2.</sub> The structure of the one-layer oxide slab is strongly distorted at the interface, while the thicker TiO<sub>2</sub> layer preserves the rutile structure. The energy cost for the formation of a single O vacancy in the one-layer oxide slab is only 0.5 eV with respect to the ideal interface. For the two-layer oxide slab, the introduction of several vacancies in an already non-stoichiometric system becomes progressively more favourable, which indicates the stability of the highly non-stoichiometric interfaces. Isolated water molecules dissociate when adsorbed at the TiO<sub>2</sub> layers. At higher coverages the preference is for molecular water adsorption. Our ab initio thermodynamics calculations show the fully water covered stoichiometric models as the most stable structure at typical ambient conditions. Interfacial models with multiple vacancies are most stable at low (reducing) oxygen chemical potential values. A water monolayer adsorbs dissociatively on the highly distorted 2-layer TiO<sub>1.75</sub>-TiN interface, where the Ti<sup>3+</sup> states lying above the top of the valence band contribute to a significant reduction of the energy gap compared to the stoichiometric TiO<sub>2</sub>-TiN model. Our results provide a guide for the design of novel interfacial systems containing ultrathin TiO<sub>2</sub> with potential application as photocatalytic water splitting devices.</p><p></p>


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