Time-dependent uptake of NO3 by sea salt
Using a coated-insert flow tube reactor coupled to a low-energy electron-impact mass spectrometer with molecular beam sampling, we studied uptake of NO 3 by sea salt at room temperature and [NO 3 ] = 8⋅10 11 − 4⋅10 13 molecule cm −3 . The radical uptake coefficient γ ( t ) is time dependent: its in...
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Veröffentlicht in: | Journal of atmospheric chemistry 2014-03, Vol.71 (1), p.33-53 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Using a coated-insert flow tube reactor coupled to a low-energy electron-impact mass spectrometer with molecular beam sampling, we studied uptake of NO
3
by sea salt at room temperature and [NO
3
] = 8⋅10
11
− 4⋅10
13
molecule cm
−3
. The radical uptake coefficient
γ
(
t
) is time dependent: its initial value (
γ
ini
) decreases exponentially with the characteristic time (
τ
) to its steady-state value (
γ
ss
) at given [NO
3
]. The parameters
γ
ini
,
γ
ss
and
τ
depend on [NO
3
], whereas
γ
ss
is water vapor independent at [H
2
O] = 8⋅10
12
− 1.6⋅10
15
molecule cm
−3
and RH ≤ 0.5 %. HCl and NO
2
are uptake products detected in the gas phase. We used these findings to estimate
γ
values under tropospheric conditions for urban coastal and remote marine environments: at high NO
3
(~90 ppt), the time dependence becomes important, and the
γ
value averaged over the aerosol lifetime is 4⋅10
−3
; at low NO
3
(~1 ppt), the radical uptake is time independent and proceeds faster with
γ
ini
= 8⋅10
−3 |
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ISSN: | 0167-7764 1573-0662 |
DOI: | 10.1007/s10874-014-9279-8 |