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Rapid growth of new atmospheric particles by nitric acid and ammonia condensation

AbstractA list of authors and their affiliations appears at the end of the paper New-particle formation is a major contributor to urban smog1,2, but how it occurs in cities is often puzzling3. If the growth rates of urban particles are similar to those found in cleaner environments (1–10 nanometres per hour), then existing understanding suggests that new urban particles should be rapidly scavenged by the high concentration of pre-existing particles. Here we show, through experiments performed under atmospheric conditions in the CLOUD chamber at CERN, that below about +5 degrees Celsius, nitric acid and ammonia vapours can condense onto freshly nucleated particles as small as a few nanometres in diameter. Moreover, when it is cold enough (below −15 degrees Celsius), nitric acid and ammonia can nucleate directly through an acid–base stabilization mechanism to form ammonium nitrate particles. Given that these vapours are often one thousand times more abundant than sulfuric acid, the resulting particle growth rates can be extremely high, reaching well above 100 nanometres per hour. However, these high growth rates require the gas-particle ammonium nitrate system to be out of equilibrium in order to sustain gas-phase supersaturations. In view of the strong temperature dependence that we measure for the gas-phase supersaturations, we expect such transient conditions to occur in inhomogeneous urban settings, especially in wintertime, driven by vertical mixing and by strong local sources such as traffic. Even though rapid growth from nitric acid and ammonia condensation may last for only a few minutes, it is nonetheless fast enough to shepherd freshly nucleated particles through the smallest size range where they are most vulnerable to scavenging loss, thus greatly increasing their survival probability. We also expect nitric acid and ammonia nucleation and rapid growth to be important in the relatively clean and cold upper free troposphere, where ammonia can be convected from the continental boundary layer and nitric acid is abundant from electrical storms4,5.
- Johann Wolfgang Goethe-Universitaet Germany
- Tampere University Finland
- Goethe University Frankfurt Germany
- Helsinki Institute of Physics Finland
- University of Colorado Boulder United States
570, 550, FORMATION EVENTS, DICARBOXYLIC-ACIDS, 103008 Experimentalphysik, 103039 Aerosol physics, 114 Physical sciences, GAS-PHASE, Article, 114, SULFURIC-ACID, AQUEOUS-SOLUTIONS, Atmospheric science, Climate change, 103039 Aerosolphysik, THERMODYNAMIC MODELS, ORGANIC-COMPOUNDS, NUMBER SIZE DISTRIBUTION, info:eu-repo/classification/ddc/550, 103008 Experimental physics, ddc:550, INORGANIC ELECTROLYTES, Physical sciences, Earth sciences, 669, 306, 103037 Environmental physics, AEROSOL FORMATION, 103037 Umweltphysik, ddc: ddc:550
570, 550, FORMATION EVENTS, DICARBOXYLIC-ACIDS, 103008 Experimentalphysik, 103039 Aerosol physics, 114 Physical sciences, GAS-PHASE, Article, 114, SULFURIC-ACID, AQUEOUS-SOLUTIONS, Atmospheric science, Climate change, 103039 Aerosolphysik, THERMODYNAMIC MODELS, ORGANIC-COMPOUNDS, NUMBER SIZE DISTRIBUTION, info:eu-repo/classification/ddc/550, 103008 Experimental physics, ddc:550, INORGANIC ELECTROLYTES, Physical sciences, Earth sciences, 669, 306, 103037 Environmental physics, AEROSOL FORMATION, 103037 Umweltphysik, ddc: ddc:550
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