We find that atmospherically relevant ammonia mixing ratios of 100 parts per trillion by volume, or less, increase
the nucleation rate of sulphuric acid particles more than 100 — 1,000-fold.
They find that atmospherically relevant ammonia mixing ratios of 100 parts per trillion by volume increase
the nucleation rate of sulphuric acid particles by more than a factor of 100 to 1,000.
the homogeneous
nucleation rate of drops nucleation in supersaturated vapor (Eqn.
► Ions enhance
the nucleation rate of stable clusters and the initial growth rate.
«Ground - level GCR ionization substantially increases
the nucleation rate of sulphuric acid and sulphuric acid — ammonia particles, by between twofold and tenfold or more, provided that the nucleation rate lies below the limiting ion - pair production rate.»
Not exact matches
«If there is too little
of either component then
nucleation will not occur at an appreciable
rate in the low atmosphere,» says Kirkby.
By performing experiments in the precisely controlled environment
of the CLOUD chamber, the project's scientists can change the concentrations
of chemicals involved in
nucleation and then measure the
rate at which new particles are created with extreme precision.
Although scientists have observed that the
nucleation process nearly always involves sulfuric acid, sulfuric acid concentrations aren't high enough to explain the
rate of new particle formation that occurs in the atmosphere.
A paper discussing the difficulty
of getting from nm sized
nucleation mode to a size that can generate cloud particles is: Erupe, M. E., et al. (2010), Correlation
of aerosol
nucleation rate with sulfuric acid and ammonia in Kent, Ohio: An atmospheric observation, J. Geophys.
The suggestion from the text is that
nucleation rates obey Boltzmann statistics generally but in certain conditions
of high surfactant loads and low tempertures the governing
rates have Bose - Einstein statistics.
«In addition we demonstrate that the binary H2SO4 — H2O
nucleation scheme, as it is usually considered in modeling studies, underestimates by 7 to 8 orders
of magnitude the observed particle formation
rate and, therefore, should not be applied in tropospheric conditions.»
The variability
of atmospheric ionization
rates due to GCR changes can be considered relatively well quantified (Bazilevskaya et al., 2008), whereas resulting changes in aerosol
nucleation rates are very poorly known (Enghoff and Svensmark, 2008; Kazil et al., 2008).
A high - voltage clearing field could also be used to remove all ions from the CLOUD chamber, meaning that the neutral
nucleation rate could be measured and compared with
nucleation enhanced by the presence
of ions.
100 ppt
of ammonia led to a 100 — 1000-fold increase in the
nucleation rate, while ground - level cosmic ray intensities were found to increase the
nucleation rate by up to a factor
of 10 (Kirkby et al. 2011).
This lowers the probability that the particles will survive to CCN sizes, and as a result it reduces the sensitivity
of CCN concentrations to changes in the
nucleation rate (Pierce & Adams 2009).
In the article «Global atmospheric particle formation from CERN CLOUD measurements,» sciencemag.org, 49 authors concluded «Atmospheric aerosol
nucleation has been studied for over 20 years, but the difficulty
of performing laboratory
nucleation -
rate measurements close to atmospheric conditions means that global model simulations have not been directly based on experimental data.....
The CERN CLOUD measurements are the most comprehensive laboratory measurements
of aerosol
nucleation rates so far achieved, and the only measurements under conditions equivalent to the free and upper troposphere.»
Ions increase the
nucleation rate by an additional factor
of between two and more than ten at ground - level galactic - cosmic - ray intensities, provided that the
nucleation rate lies below the limiting ion - pair production
rate.
Model calculations suggest that almost half
of the global cloud condensation nuclei in the atmospheric boundary layer may originate from the
nucleation of aerosols from trace condensable vapours4, although the sensitivity
of the number
of cloud condensation nuclei to changes
of nucleation rate may be small5, 6.
However, even with the large enhancements in
rate due to ammonia and ions, atmospheric concentrations
of ammonia and sulphuric acid are insufficient to account for observed boundary - layer
nucleation.
Even with the large enhancements in
rate caused by ammonia and ions, they conclude that atmospheric concentrations
of ammonia and sulphuric acid are insufficient to account for observed boundary layer
nucleation.
He ignores the possibility that decadal variability may be caused by external forcing such as cosmic rays which are known to cause increased
rates of aerosol
nucleation.