CO levels showed the most significant reductions during the partial lockdown.• NO 2 decreased in a lower extent, due to industrial and diesel input. • PM 10 levels were only reduced during the first partial lockout week. • Ozone increased due to the decrease in nitrogen oxides level in a VOCcontrolled scenario.

Abstract. Social distancing to combat the COVID-19 pandemic has led to widespread reductions in air pollutant emissions. Quantifying these changes requires a business-as-usual counterfactual that accounts for the synoptic and seasonal variability of air pollutants. We use a machine learning algorithm driven by information from the NASA GEOS-CF model to assess changes in nitrogen dioxide (NO2) and ozone (O3) at 5756 observation sites in 46 countries from January through June 2020. Reductions in NO2 coincide with the timing and intensity of COVID-19 restrictions, ranging from 60 % in severely affected cities (e.g., Wuhan, Milan) to little change (e.g., Rio de Janeiro, Taipei). On average, NO2 concentrations were 18 (13–23) % lower than business as usual from February 2020 onward. China experienced the earliest and steepest decline, but concentrations since April have mostly recovered and remained within 5 % of the business-as-usual estimate. NO2 reductions in Europe and the US have been more gradual, with a halting recovery starting in late March. We estimate that the global NOx (NO + NO2) emission reduction during the first 6 months of 2020 amounted to 3.1 (2.6–3.6) TgN, equivalent to 5.5 (4.7–6.4) % of the annual anthropogenic total. The response of surface O3 is complicated by competing influences of nonlinear atmospheric chemistry. While surface O3 increased by up to 50 % in some locations, we find the overall net impact on daily average O3 between February–June 2020 to be small. However, our analysis indicates a flattening of the O3 diurnal cycle with an increase in nighttime ozone due to reduced titration and a decrease in daytime ozone, reflecting a reduction in photochemical production. The O3 response is dependent on season, timescale, and environment, with declines in surface O3 forecasted if NOx emission reductions continue.

Abstract. Social-distancing to combat the COVID-19 pandemic has led to widespread reductions in air pollutant emissions. Quantifying these changes requires a business as usual counterfactual that accounts for the synoptic and seasonal variability of air pollutants. We use a machine learning algorithm driven by information from the NASA GEOS-CF model to assess changes in nitrogen dioxide (NO2) and ozone (O3) at 5756 observation sites in 46 countries from January through June 2020. Reductions in NO2 correlate with timing and intensity of COVID-19 restrictions, ranging from 60 % in severely affected cities (e.g., Wuhan, Milan) to little change (e.g., Rio de Janeiro, Taipei). On average, NO2 concentrations were 18 % lower than business as usual from February 2020 onward. China experienced the earliest and steepest decline, but concentrations since April have mostly recovered and remained within 5 % to the business as usual estimate. NO2 reductions in Europe and the US have been more gradual with a halting recovery starting in late March. We estimate that the global NOx (NO + NO2) emission reduction during the first 6 months of 2020 amounted to 2.9 TgN, equivalent to 5.1 % of the annual anthropogenic total. The response of surface O3 is complicated by competing influences of non-linear atmospheric chemistry. While surface O3 increased by up to 50 % in some locations, we find the overall net impact on daily average O3 between February–June 2020 to be small. However, our analysis indicates a flattening of the O3 diurnal cycle with an increase in night time ozone due to reduced titration and a decrease in daytime ozone, reflecting a reduction in photochemical production. The O3 response is dependent on season, time scale, and environment, with declines in surface O3 forecasted if NOx emission reductions continue.

Phase equilibrium behavior of the system castor oil biodiesel + glycerol + methanol was studied to provide experimental data for the optimization of the separation downstream processes. Measurements of solubility were carried out for the ternary systems containing biodiesel derived from castor + glycerol + methanol at 298.15 K and + ethanol at (298.15 and 333.15) K. An increase of the system mutual solubility was observed with temperature. Binodal curves were determined by the cloud point using the titration method under isothermal conditions. The tie-lines for biodiesel + glycerol + methanol at 298.15 K were indirectly measured by analyzing the mixture density. The Othmer-Tobias correlation was used to ascertain the consistency of tie-line data. The results were correlated with the UNIQUAC model satisfactorily.

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