Journal
ENVIRONMENTAL SCIENCE-ATMOSPHERES
Volume 2, Issue 3, Pages 441-448Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ea00104c
Keywords
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Funding
- Carl Tryggers Foundation
- EU [847693]
- FAPESP (the Sao Paulo Research Foundation) [2017/11986-5]
- Shell
- ANP (Brazil's National Oil, Natural Gas and Biofuels Agency) through the R&D levy regulation
- National Council for Scientific and Technological Development [CNPq 401581/2016-0]
- Swedish-Brazilian collaboration STINT-CAPES [9805/2014-01]
- Swedish Research Council [2018-00740, 2017-04162]
- Helmholtz Association through the Center for Free-Electron Laser Science at DESY
- Swedish Research Council [2017-04162, 2018-00740] Funding Source: Swedish Research Council
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In this study, we used photoelectron spectroscopy to investigate the change in surface composition of aqueous solutions at different pH values. We found that the relative distribution of inorganic ions at the liquid water surface changed by a factor of 4-5, which was attributed to ion pairing and the formation of charged layers.
In atmospheric aerosol particles, the chemical surface composition governs both heterogenous chemical reactions with gas-phase species and the ability to act as nuclei for cloud droplets. The pH in aerosol particles is expected to affect these properties, but it is very challenging to measure the pH in individual droplets, precluding the investigation of its influence on the particle's surface composition. In this work, we use photoelectron spectroscopy to explore how the surface composition of aqueous solutions containing inorganic salt and amino acids changes as a function of pH. We observe a change by a factor of 4-5 of the relative distribution of inorganic ions at the surface of a liquid water jet, as a function of solution pH and type of amino acid in the solution. The driving forces for the surface enhancement or depletion are ion pairing and the formation of charged layers close to the aqueous surface.
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