Matrix effect on surface-catalyzed photolysis of nitric acid
Photolysis rate constant of HNO 3 on the surface (HNO 3(s) ) has been found to be enhanced by 1–4 orders of magnitude from that of gaseous HNO 3 , with HONO and NO 2 as the main products. Such Re-NOx-ification pathway extends the apparent lifetime of reactive nitrogen species and modifies the atmosp...
Saved in:
Published in | Scientific reports Vol. 9; no. 1; p. 4351 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
13.03.2019
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Photolysis rate constant of HNO
3
on the surface (HNO
3(s)
) has been found to be enhanced by 1–4 orders of magnitude from that of gaseous HNO
3
, with HONO and NO
2
as the main products. Such Re-NOx-ification pathway extends the apparent lifetime of reactive nitrogen species and modifies the atmospheric oxidative capacity along its long-rang transport. Despite of its importance, the detailed kinetics and mechanisms of HNO
3(s)
photolysis are still not clear. Surface film of HNO
3
and organic compounds is ubiquitous in the environment and imposes matrix effect on HNO
3(s)
photolysis. Here we studied photolysis of HNO
3
on Pyrex glass in a photochemical flow reactor over a wide range of HNO
3
surface density (
D
HNO3
) with or without the presence of model organic compounds. The photolysis rate constant of HNO
3(s)
varied with
D
HNO3
and surface-catalysis mechanism was proposed. Organic compounds further enhance the photolysis rate constant by up to one order of magnitude via both photosensitization and H-donating reaction. The H-donating reaction enhances as well the secondary HONO yield from reaction between the primary product NO
2
and adjacent H-donor, and thus increases the HONO/NO
2
production ratio. Finally, detailed mechanisms involving surface-catalyisis, photosensitization and H-donating reactions was integrated. |
---|---|
ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-018-37973-x |