Title of article :
Night-time radical chemistry during the TORCH campaign
Author/Authors :
Emmerson، نويسنده , , K.M. and Carslaw، نويسنده , , N.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2009
Pages :
7
From page :
3220
To page :
3226
Abstract :
We present one of the most comprehensive studies of night-time radical chemistry to date, from the Tropospheric ORganic CHemistry experiment (TORCH) in the summer of 2003. TORCH provided a wealth of measurements with which to study the oxidizing capacity of the atmosphere. The measurements provided input to a zero-dimensional box model which has been used to study night-time radical chemistry during the campaign. Average night-time predicted concentrations of OH (2.6 × 105 molecule cm−3), HO2 (2.9 × 107 molecule cm−3) and [HO2+ΣRO2] radicals (2.2 × 108 molecule cm−3) were an order of magnitude smaller than those predicted during the daytime. The model under-predicted the night-time measurements of OH, HO2 and [HO2+ΣRO2] radicals, on average by 41%, 16% and 8% respectively. Whilst the model captured the broad features of night-time radical behaviour, some of the specific features that were observed are hard to explain. A rate of radical production assessment was carried out for the whole campaign between the hours of 00:00 and 04:00. Whilst radical production was limited owing to the absence of photolytic reactions, production routes via the reactions of alkenes with O3 provided an effective night-time radical source. Nitrate radical concentrations were predicted to be 0.6 ppt on average with a peak of 18 ppt on August 9th during a polluted heat wave period. Overall, the nitrate radical contributes about a third of the total initiation via RO2, mostly through reaction with alkenes.
Keywords :
Hydroxyl radical , Tropospheric modelling , Night-time chemistry , nitrate radical
Journal title :
Atmospheric Environment
Serial Year :
2009
Journal title :
Atmospheric Environment
Record number :
2235073
Link To Document :
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