The effect upon the photostationary state relationship when clean air and photochemical smog mix

1980 ◽  
Vol 14 (12) ◽  
pp. 1445-1448 ◽  
Author(s):  
D.J. Kewley
2015 ◽  
Vol 15 (16) ◽  
pp. 22097-22139 ◽  
Author(s):  
J. D. Lee ◽  
L. K. Whalley ◽  
D. E. Heard ◽  
D. Stone ◽  
R. E. Dunmore ◽  
...  

Abstract. Measurements of HONO were carried out at an urban background site near central London as part of the Clean air for London (ClearfLo) project in summer 2012. Data was collected from 22 July–18 August 2014, with peak values of up to 1.8 ppbV at night and non-zero values of between 0.2 and 0.6 ppbV seen during the day. A wide range of other gas phase, aerosol, radiation and meteorological measurements were made concurrently at the same site, allowing a detailed analysis of the chemistry to be carried out. The peak HONO/NOx ratio of 0.04 is seen at ~ 02:00 UTC, with the presence of a second, daytime peak in HONO/NOx of similar magnitude to the night-time peak suggesting a significant secondary daytime HONO source. A photostationary state calculation of HONO involving formation from the reaction of OH and NO and loss from photolysis, reaction with OH and dry deposition shows a significant underestimation during the day, with calculated values being close to zero, compared to the measurement average of 0.4 ppbV at midday. The addition of further HONO sources, including postulated formation from the reaction of HO2 with NO2 and photolysis of HNO3, increases the daytime modelled HONO to 0.1 ppbV, still leaving a significant extra daytime source. The missing HONO is plotted against a series of parameters including NO2 and OH reactivity, with little correlation seen. Much better correlation is observed with the product of these species with j(NO2), in particular NO2 and the product of NO2 with OH reactivity. This suggests the missing HONO source is in some way related to NO2 and also requires sunlight. The effect of the missing HONO to OH radical production is also investigated and it is shown that the model needs to be constrained to measured HONO in order to accurately reproduce the OH radical measurements.


2016 ◽  
Vol 16 (5) ◽  
pp. 2747-2764 ◽  
Author(s):  
J. D. Lee ◽  
L. K. Whalley ◽  
D. E. Heard ◽  
D. Stone ◽  
R. E. Dunmore ◽  
...  

Abstract. Measurements of HONO were carried out at an urban background site near central London as part of the Clean air for London (ClearfLo) project in summer 2012. Data were collected from 22 July to 18 August 2014, with peak values of up to 1.8 ppbV at night and non-zero values of between 0.2 and 0.6 ppbV seen during the day. A wide range of other gas phase, aerosol, radiation, and meteorological measurements were made concurrently at the same site, allowing a detailed analysis of the chemistry to be carried out. The peak HONO/NOx ratio of 0.04 is seen at  ∼  02:00 UTC, with the presence of a second, daytime, peak in HONO/NOx of similar magnitude to the night-time peak, suggesting a significant secondary daytime HONO source. A photostationary state calculation of HONO involving formation from the reaction of OH and NO and loss from photolysis, reaction with OH, and dry deposition shows a significant underestimation during the day, with calculated values being close to 0, compared to the measurement average of 0.4 ppbV at midday. The addition of further HONO sources from the literature, including dark conversion of NO2 on surfaces, direct emission, photolysis of ortho-substituted nitrophenols, the postulated formation from the reaction of HO2 ×  H2O with NO2, photolysis of adsorbed HNO3 on ground and aerosols, and HONO produced by photosensitized conversion of NO2 on the surface increases the daytime modelled HONO to 0.1 ppbV, still leaving a significant missing daytime source. The missing HONO is plotted against a series of parameters including NO2 and OH reactivity (used as a proxy for organic material), with little correlation seen. Much better correlation is observed with the product of these species with j(NO2), in particular NO2 and the product of NO2 with OH reactivity. This suggests the missing HONO source is in some way related to NO2 and also requires sunlight. Increasing the photosensitized surface conversion rate of NO2 by a factor of 10 to a mean daytime first-order loss of  ∼ 6 × 10−5 s−1 (but which varies as a function of j(NO2)) closes the daytime HONO budget at all times (apart from the late afternoon), suggesting that urban surfaces may enhance this photosensitized source. The effect of the missing HONO to OH radical production is also investigated and it is shown that the model needs to be constrained to measured HONO in order to accurately reproduce the OH radical measurements.


1989 ◽  
Vol 67 (7) ◽  
pp. 2175-2181 ◽  
Author(s):  
Andrzej Bytnerowicz ◽  
David M. Olszyk ◽  
Satu Huttunen ◽  
Brent Takemoto

One-year-old seedlings of Pinus coulteri, P. pondersosa, P. jeffreyi, and P. sylvestris were exposed for 5 months to ambient photochemical smog (average 24-h monthly concentrations of ozone 0.067 to 0.108 ppm) in the San Gabriel Mountains of the Los Angeles Basin. Plants were grown in open-top chambers ("ambient-air" and "clean-air" treatments) and in outside plots. Rinsing of needles as well as scanning electron microscope observations revealed the highest deposition of particles to plants in the outside plots. No significant changes in growth in any of the studied species were observed. Exposure to photochemical smog had no significant effect on net photosynthesis and dark respiration in P. coulteri and P. ponderosa. Visual observation of injury showed that, by the end of the exposures, the P. ponderosa foliage in the ambient-air treatments was more damaged than in the clean-air treatment, but no negative effects on P. coulteri and P. jeffreyi foliage were seen. A tendency towards greater injury of P. sylvestris foliage in the ambient-air chambers and in the outside plots was also determined. Scanning electron microscope observations showed some subtle changes in the surface of P. coulteri and P. sylvestris in the ambient air treatment. Longer, multiseasonal exposures seem to be needed to study the effects of ambient concentrations of photochemical pollutants on forest trees.


1992 ◽  
Vol 02 (04) ◽  
pp. 665-678 ◽  
Author(s):  
M. Kasahara ◽  
K-.C. Choi ◽  
K. Takahashi

More than 3,000 aerosol samples have been collected since 1986 in Kyoto under various meteorological and environmental conditions, including episodic air pollution events such as heavy air pollution, Kosa dust, very clean air, etc. The elemental concentrations of these aerosol samples were determined by PIXE techniques, and elemental concetration data were used to estimate a source contribution of aerosols by applying a receptor model. The concentrations of Si, K, Ca, Ti and Fe in both coarse and fine fractions increased tremendously at Kosa event. The maximum source contribution of soil dust amounted to 140 μg/m3 for a six hour average during a Kosa event. On the other hand, the concentrations of S, Zn, Pb and Cu in the fine fraction increased remarkably during heavy air pollution and photochemical smog events.


Author(s):  
Hongrong Shi ◽  
Jinqiang Zhang ◽  
Bin Zhao ◽  
Xiangao Xia ◽  
Bo Hu ◽  
...  
Keyword(s):  

1970 ◽  
Author(s):  
ALAN ESCI-LENFLOEDER ◽  
JOSE MARTINEZ
Keyword(s):  

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