Presentation is loading. Please wait.

Presentation is loading. Please wait.

Center for Environmental Research and Technology University of California, Riverside Bourns College of Engineering Evaluation and Intercomparison of N.

Similar presentations


Presentation on theme: "Center for Environmental Research and Technology University of California, Riverside Bourns College of Engineering Evaluation and Intercomparison of N."— Presentation transcript:

1 Center for Environmental Research and Technology University of California, Riverside Bourns College of Engineering Evaluation and Intercomparison of N 2 O 5 Chemistry in Two Versions of CMAQ Chao-Jung Chien, Gail S. Tonnesen, Bo Wang, Zion S. Wang and Mohammad Omary OVERVIEW The impact of tropospheric dinitrogen pentoxide (N 2 O 5 ) on the global distribution of nitrogen oxides (NOx), ozone (O 3 ) and hydroxyl radical (OH) has been well recognized (Dentener et al. JGR, v101, p.22869, 1996). Gaseous N 2 O 5 reacts with water to form nitric acid (HNO 3 ) both in the gas phase and on surfaces (reactions and ). While the reaction of N 2 O 5 in the gas phase is relatively slow, with rate constant of ~10 -21 cm 3 molecule -1 s -1, it has been shown the heterogeneously hydrolyzed N 2 O 5 could release up to 70% of HNO3 into the gas phase (Wahner et al., JGR., v.103, p.31103, 1998). N 2 O 5 + H 2 O  2 HNO 3 N 2 O 5 + H 2 O (aerosol)  2 HNO 3 US EPA has recently released its latest version of the Community Multiscale Air Quality (CMAQ) modeling system in June, 2002. Unlike the previous version (released in March, 2001, v.0301) which treats hydrolysis of N 2 O 5 exclusively in the gas phase, the new release (v.0602) includes heterogeneous conversion of N 2 O 5 to HNO 3 on aerosol surfaces. In this study, we evaluate CMAQ performance against available ambient measurements, and compare the contributing chemical processes using process analysis for both versions of CMAQ. Other major reactions ( and ) that convert NOx to HNO 3, the major sink for reactive NOx, are also examined. OH + NO 2  HNO 3 VOC + NO 3  RO 2 + HNO 3 CONCLUSIONS New CMAQ shows more overproduction of nitrate than previous version in both January and July. Time-series plots for each reaction indicate diurnal changes for each processes: dominant nighttime production of HNO 3 from heterogeneous conversion of N 2 O 5. Nocturnal heterogeneous conversion of N 2 O 5 to HNO 3 on aerosols accounts for up to 70% and 30% of the diurnal HNO 3 formation for New CMAQ in January and July, respectively (generally consistent with Dentener et al.). New CMAQ model performance is worse. It is uncertain whether the new N 2 O 5 chemistry is wrong or if errors in other model inputs or ambient data are responsible for the poor model performance. Method 1.Model description and comparisons: Modified rate constant for reaction in new CMAQ. Implementation of heterogeneous conversion of N 2 O 5 to nitric acid in new CMAQ (reaction ):  Based on studies by Dentener and Crutzen (JGR, v.98, p.7149, 1993): N 2 O 5 + H 2 O  2HNO 3 where k is the pseudo-first order reaction coefficient (s -1 ); r is the aerosol radius (cm); D g (cm 2 s -1 ) is the gas phase diffusion coefficient, calculated according to Fuller et al. (J. Phys. Chem., v.75, p.3679, 1969);  is the reaction probability on surface particles ( r =0.1 for N2O5); v is the mean molecular speed (cm s -1 ); and A is the aerosol surface, (cm 2 aerosol)/(cm3 air). RESULTS 3.Integrated reaction rate (IRR) analysis of two CMAQs: Comparing process analysis outputs from CMAQs in mass based units (moles) on cumulative results (each day or 14 days total) Codes modified in new CMAQ (aero_subs.f) to extract information of HNO3 production from heterogeneous conversion of N 2 O 5. 2.CMAQ Simulations: WRAP domain: 85 columns, 95 rows, 18 layers, 36km grid cells horizontally; 68 variables Meteorology: MM5 1996 simulation, processed with MCIP v.2 Modeling period: January: 14-31 July: 18-31 (Julian dates 200-213) Spin-up periods Jan 1-13 & July 1-17 k aerosol 2.Model Evaluation with Ambient Database Database:  IMPROVE: 49 stations in January and July, 1996  CASTNET: 25 stations in July, 1996 (limited data in January) CMAQ species:  ANO 3 (IMPROVE, CASTNET), HNO 3 (CASTNET), Total nitrates (CASTNET) Scatter plots  AllSites_AllDays (Figures)  Statistical analysis: Regression (r-squared), Mean normalized bias (MNB%) and error (MNE%) Model predictions vs. IMPROVE for Aerosol NO3 in JanuaryModel predictions vs. IMPROVE for Aerosol NO3 in July Model predictions vs. CASTNET for Gaseous HNO3 in JulyModel predictions vs. CASTNET for total nitrate (ANO3+HNO3) in July Time series plots for major chemical pathways contributing to HNO 3 production. Summary of total HNO 3 production for full domain on each day and for both versions of CMAQ IRR total HNO 3 production summed for full domain and all days for both versions of CMAQ. Difference in HNO 3 production between conversion of N 2 O 5 from New CMAQ (gas + aerosol phases) and Old CMAQ (gas phase only). Plots are cumulative for one day in January and July. Jan.July Jan.July Emissions processing: SMOKE: Mobil: version D; Area, Point, Biogenic: version E CCTM modules: QSSA with Process Analysis (Procan) Chem: CB-IV with aqueous and aerosol extensions: CB4_AE2_AQ (old CMAQ) vs. CB4_AE3_AQ (new CMAQ) 1.Difference plots in mixing ratio (ppbv) between new and old CMAQs for model species: O 3, HNO 3, and aerosol nitrate (ANO 3 ) in both January and July. Old New Old New


Download ppt "Center for Environmental Research and Technology University of California, Riverside Bourns College of Engineering Evaluation and Intercomparison of N."

Similar presentations


Ads by Google