WRF-Chem model predictions of the regional impacts of N2O5 heterogeneous processes on night-time chemistry over north-western Europe

D Lowe, S Archer-Nicholls, W Morgan, J Allan, S Utembe, B Ouyang, E Aruffo, M Le Breton, R A Zaveri, P Di Carlo, C Percival, H Coe, R Jones, Gordon Mcfiggans

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Chemical modelling studies have been conducted over north-western Europe in summer conditions, showing that night-time dinitrogen pentoxide (N2O5) heterogeneous reactive uptake is important regionally in modulating particulate nitrate and has a modest influence on oxidative chemistry. Results from Weather Research and Forecasting model with Chemistry (WRF-Chem) model simulations, run with a detailed volatile organic compound (VOC) gas-phase chemistry scheme and the Model for Simulating Aerosol Interactions and Chemistry (MOSAIC) sectional aerosol scheme, were compared with a series of airborne gas and particulate measurements made over the UK in July 2010. Modelled mixing ratios of key gas-phase species were reasonably accurate (correlations with measurements of 0.7-0.9 for NO2 and O-3). However modelled loadings of particulate species were less accurate (correlation with measurements for particulate sulfate and ammonium were between 0.0 and 0.6). Sulfate mass loadings were particularly low (modelled means of 0.5-0.7 mu gkg(air)(-1), compared with measurements of 1.0-1.5 mu gkg(air)(-1)). Two flights from the campaign were used as test cases - one with low relative humidity (RH) (60-70 \%), the other with high RH (80-90 \%). N2O5 heterogeneous chemistry was found to not be important in the low-RH test case; but in the high-RH test case it had a strong effect and significantly improved the agreement between modelled and measured NO3 and N2O5. When the model failed to capture atmospheric RH correctly, the modelled NO3 and N2O5 mixing ratios for these flights differed significantly from the measurements. This demonstrates that, for regional modelling which involves heterogeneous processes, it is essential to capture the ambient temperature and water vapour profiles. The night-time NO3 oxidation of VOCs across the whole region was found to be 100-300 times slower than the day-time OH oxidation of these compounds. The difference in contribution was less for alkenes (x80) and comparable for dimethylsulfide (DMS). However the suppression of NO3 mixing ratios across the domain by N2O5 heterogeneous chemistry has only a very slight, negative, influence on this oxidative capacity. The influence on regional particulate nitrate mass loadings is stronger. Night-time N2O5 heterogeneous chemistry maintains the production of particulate nitrate within polluted regions: when this process is taken into consideration, the daytime peak (for the 95th percentile) of PM10 nitrate mass loadings remains around 5.6 mu gkg(air)(-1), but the night-time minimum increases from 3.5 to 4.6 mu gkg(air)(-1). The sustaining of higher particulate mass loadings through the night by this process improves model skill at matching measured aerosol nitrate diurnal cycles and will negatively impact on regional air quality, requiring this process to be included in regional models.
    Original languageEnglish
    Pages (from-to)1385-1409
    Number of pages25
    JournalAtmospheric Chemistry and Physics
    Volume15
    Issue number3
    DOIs
    Publication statusPublished - 2015

    Keywords

    • intermediates cri mechanism
    • secondary organic aerosol
    • size distributions
    • atmospheric chemistry
    • mass-spectrometer
    • o-x
    • nitrate
    • parameterization
    • no3
    • reanalysis

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