Aerosol pH and its driving factors in Beijing
2019
Abstract. Aerosol acidity plays a key role in secondary aerosol formation. The
high-temporal-resolution PM 2.5 pH and size-resolved aerosol pH in
Beijing were calculated with ISORROPIA II. In 2016–2017, the mean PM 2.5
pH (at relative humidity (RH) > 30 %) over four seasons was
4.5±0.7 (winter) > 4.4±1.2 (spring) > 4.3±0.8 (autumn) > 3.8±1.2 (summer), showing
moderate acidity. In coarse-mode aerosols, Ca 2+ played an important
role in aerosol pH. Under heavily polluted conditions, more secondary ions
accumulated in the coarse mode, leading to the acidity of the coarse-mode
aerosols shifting from neutral to weakly acidic. Sensitivity tests also
demonstrated the significant contribution of crustal ions to PM 2.5 pH.
In the North China Plain (NCP), the common driving factors affecting
PM 2.5 pH variation in all four seasons were SO 4 2 - , TNH 3
(total ammonium (gas + aerosol)), and temperature, while unique factors
were Ca 2+ in spring and RH in summer. The decreasing SO 4 2 -
and increasing NO 3 - mass fractions in PM 2.5 as well as
excessive NH 3 in the atmosphere in the NCP in recent years are the
reasons why aerosol acidity in China is lower than that in Europe and the
United States. The nonlinear relationship between PM 2.5 pH and
TNH 3 indicated that although NH 3 in the NCP was abundant, the
PM 2.5 pH was still acidic because of the thermodynamic equilibrium
between NH 4 + and NH 3 . To reduce nitrate by controlling
ammonia, the amount of ammonia must be greatly reduced below excessive
quantities.
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