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O
O 2
CH 3 CCH 2 ONO 2
+ HO 2
α -(nitrooxy)acetone
OO
O
RO 2
NO 3
O 2
CH 3 CHCH 2 ONO 2
CH 3 CCHCH 2 ONO 2
M
NO 3
NO 2
PDDN
CH 3 CHO + HCHO
+ NO 2
M
NO 3
ONO 2
ONO 2
RO 2
NO 3
CH 3 CHCH 2 O 2
O 2
CH 3 CHCH 2 O
NO 2
NPPN
Figure 15 A schematic representation of the chain propagation reactions in the NO 3
radical initiated oxidation of propene 28
Aerosol surface
reactions
Organic nitrates
N 2 O 5
NO 2
Alkenes
O 3
O 3
NO 3
H 2 O
NO 2
Aerosol
losses
RH,
DMS
NO, RO 2
Surface losses
HNO 3
Figure 16 A simplified reaction scheme for night-time chemistry involving the nitrate
radical 27
significant regeneration of NO x and production of unsubstituted car-
bonyl products while comparatively they are a minor source of HO x . 28
For the less alkyl substituted alkenes, there is a greater yield of HO x and
bifunctional organic nitrate products but a lesser regeneration of NO x .
Therefore, depending on the mix of hydrocarbons, NO 3 chemistry can
act to either recycle NO x , therefore inhibiting the formation of nitrate
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