Influence of Fog-Haze on Dew Condensation in Urban Areas

In recent years, fog-haze weather has frequently occurred in urban ecosystem, with accompanied dew condensation in the surface layer. Dew formation plays an important role in air purification, which takes fine aerosols in the atmosphere as the condensation nuclei. However, the influence of fog-haze on dew condensation remains unclear. Thus, this study aims to evaluate the influences of fog-haze days on the frequency, intensity, and duration of dew condensation, to reveal the factors relevant to dew condensation during weather pollution, and to improve the air quality in fog-haze days. The monitor-based direct weighing method was employed in this study to observe the vapour condensation in urban greenbelt under fog-haze and normal weather conditions during the frost-free season (April-October 2017) in Changchun, China. The differences in dew condensation intensity and frequency were discriminated under different weather conditions. Then, the influences of fog-haze days on the vapour condensation were analyzed by monitoring the velocity and duration of dew condensation in polluted weather. Finally, a program for improving air quality was proposed based on the analysis of major meteorological factors that affect the dew condensation during the fog-haze days. Results show that the dew condensation velocity decreases significantly (P 0.05). The particulate matter concentration, wind speed, air pressure, relative humidity, and solar radiation are the main factors that affect the vapour transport during the fog-haze days. Artificial increase of surface layer vapours can promote the particulates to absorb vapours fully and settle to the ground in the form of dew, thereby reducing the particulate matter concentration within the scope of human activities. The present study supplements the eigenvalues for dew condensation in urban areas during special pollution periods and reveals the influence of fog-haze on the night time vapour condensation in urban areas. Findings of this study provide theoretical basis for further developing the programs for controlling fog-haze weather and improving urban air quality

Increased inorganic aerosol fraction contributes to air pollution and haze in China

The detailed formation mechanism of an increased number of haze events in China is still not very clear. Here, we found that reduced surface visibility from 1980 to 2010 and an increase in satellite-derived columnar concentrations of inorganic precursors from 2002 to 2012 are connected with each other. Typically, higher inorganic mass fractions lead to increased aerosol water uptake and light-scattering ability in elevated relative humidity. Satellite observation of aerosol precursors of NO2 and SO2 showed increased concentrations during the study period. Our in situ measurement of aerosol chemical composition in Beijing also confirmed increased contribution of inorganic aerosol fraction as a function of the increased particle pollution level. Our investigations demonstrate that the increased inorganic fraction in the aerosol particles is a key component in the frequently occurring haze days during the study period, and particularly the reduction of nitrate, sulfate and their precursor gases would contribute towards better visibility in China.Peer reviewe

Mitigating NO_x emissions does not help alleviate wintertime particulate pollution in Beijing-Tianjin-Hebei (BTH), China

Stringent mitigation measures have reduced wintertime PM_(2.5) concentrations by 42.2% from 2013 to 2018 in the BTH. The observed nitrate aerosols have not exhibited a significant decreasing trend and constituted a major fraction (about 20%) of the total PM_(2.5), although the surface-measured NO₂ level has decreased by over 20%. It still remains elusive about contributions of nitrogen oxides (NO_x) emissions mitigation to the nitrate and PM_(2.5) level. The WRF-Chem model simulations of a persistent haze episode in January 2019 in the BTH reveal that NO_x emissions mitigation does not help lower wintertime nitrate and PM_(2.5) concentrations under current conditions in the BTH, because the substantial O₃ increase induced by NO_x mitigation offsets the HNO₃ loss and enhances sulfate and secondary organic aerosols formation. Our results are further consolidated by occurrence of the severe PM pollution in the BTH during the COVID-19 outbreak with a significant reduction of NO₂

Mitigating NO_x emissions does not help alleviate wintertime particulate pollution in Beijing-Tianjin-Hebei (BTH), China

Stringent mitigation measures have reduced wintertime PM_(2.5) concentrations by 42.2% from 2013 to 2018 in the BTH. The observed nitrate aerosols have not exhibited a significant decreasing trend and constituted a major fraction (about 20%) of the total PM_(2.5), although the surface-measured NO₂ level has decreased by over 20%. It still remains elusive about contributions of nitrogen oxides (NO_x) emissions mitigation to the nitrate and PM_(2.5) level. The WRF-Chem model simulations of a persistent haze episode in January 2019 in the BTH reveal that NO_x emissions mitigation does not help lower wintertime nitrate and PM_(2.5) concentrations under current conditions in the BTH, because the substantial O₃ increase induced by NO_x mitigation offsets the HNO₃ loss and enhances sulfate and secondary organic aerosols formation. Our results are further consolidated by occurrence of the severe PM pollution in the BTH during the COVID-19 outbreak with a significant reduction of NO₂

Chemistry of new particle formation and growth events during wintertime in suburban area of Beijing : Insights from highly polluted atmosphere

The high frequency of new particle formation (NPF) events observed under polluted atmospheric conditions is still poorly understood. To improve our understanding of NPF and its effects, the particle number size distribution (3-1000 nm) and submicron particle chemical composition were measured from 4 November 2017 to 17 January 2018 in suburban Beijing. During this intense campaign, 22 NPF events were identified with a frequency of 29%, including 11 cases that occurred under "clean" conditions (C-NPF) and 11 cases that occurred under "polluted" conditions (P-NPF). The observed formation rate (J(3)) and condensation sink were 4.6-148.9 cm(-3).s(-1) and 0.01-0.07 s(-1), and the majority of NPF events occurred when the condensation sink (CS) values below 0.03 s(-1), indicating that condensation vapor likely constitutes the critical limiting factor for NPF events. The correlations between log J(3) and [H2SO4] that close to previous CLOUD experimental results in the majority of NPF events (68%) suggest the high nucleation rates (up to 100 cm(-3).s(-1)) would be attributed by the amines that enhancing sulfuric acid nucleation, while the reminding cases (32%) possibly attributed to the H2SO4-NH3 clustering mechanism, which is supported by the theoretical expectations for H2SO4 nucleation with NH3 simulated by the MALTE_BOX model. The observed growth rate varied from 4.9 to 37.0 mm.h(-1), with the dominant contribution (>60%) from sulfuric acid during the early phases of growth (similar to 4 nm), which was also sufficient to explain the observed Q(GR) for 50 nm)Peer reviewe

Rapid formation of intense haze episodes via aerosol-boundary layer feedback in Beijing

Although much effort has been put into studying air pollution, our knowledge of the mechanisms of frequently occurring intense haze episodes in China is still limited. In this study, using 3 years of measurements of air pollutants at three different height levels on a 325m Beijing meteorology tower, we found that a positive aerosol-boundary layer feedback mechanism existed at three vertical observation heights during intense haze polluted periods within the mixing layer. This feedback was characterized by a higher loading of PM2.5 with a shallower mixing layer. Modelling results indicated that the presence of PM2.5 within the boundary layer led to reduced surface temperature, relative humidity and mixing layer height during an intensive haze episode. Measurements showed that the aerosol-boundary layer feedback was related to the decrease in solar radiation, turbulent kinetic energy and thereby suppression of the mixing layer. The feedback mechanism can explain the rapid formation of intense haze episodes to some extent, and we suggest that the detailed feedback mechanism warrants further investigation from both model simulations and field observations.Peer reviewe

An unexpected catalyst dominates formation and radiative forcing of regional haze

Although regional haze adversely affects human health and possibly counteracts global warming from increasing levels of greenhouse gases, the formation and radiative forcing of regional haze on climate remain uncertain. By combining field measurements, laboratory experiments, and model simulations, we show a remarkable role of black carbon (BC) particles in driving the formation and trend of regional haze. Our analysis of long-term measurements in China indicates declined frequency of heavy haze events along with significantly reduced SO₂, but negligibly alleviated haze severity. Also, no improving trend exists for moderate haze events. Our complementary laboratory experiments demonstrate that SO₂ oxidation is efficiently catalyzed on BC particles in the presence of NO₂ and NH₃, even at low SO₂ and intermediate relative humidity levels. Inclusion of the BC reaction accounts for about 90–100% and 30–50% of the sulfate production during moderate and heavy haze events, respectively. Calculations using a radiative transfer model and accounting for the sulfate formation on BC yield an invariant radiative forcing of nearly zero W m⁻² on the top of the atmosphere throughout haze development, indicating small net climatic cooling/warming but large surface cooling, atmospheric heating, and air stagnation. This BC catalytic chemistry facilitates haze development and explains the observed trends of regional haze in China. Our results imply that reduction of SO₂ alone is insufficient in mitigating haze occurrence and highlight the necessity of accurate representation of the BC chemical and radiative properties in predicting the formation and assessing the impacts of regional haze