Pioneering observation of atmospheric volatile organic compounds in Hangzhou in eastern China and implications for upcoming 2022 Asian Games

Understanding the emission sources of volatile organic compounds(VOCs)is critical for air pollution mitigation.Continuous measurements of atmospheric VOCs were conducted from January to February in Hangzhou in 2021.The average measured concentration of total VOCs(TVOCs)was 38.2±20.9 ppb,>42% lower than that reported by previous studies at the urban center in Hangzhou.The VOC concentrations and proportions were similar between weekdays and weekends.During the long holidays of the Spring Festival in China,the concentrations of TVOCs were∼50% lower than those during the regular days,but their profiles showed no significant difference(p>0.05).Further,we deduced that aromatics and alkenes were the most crucial chemicals promoting the formation of O3 and secondary organic aerosol(SOA)in Hangzhou.According to interspecies correlations,combustion processes and solvent use were inferred as major VOC emission sources.This study provides implications for air quality improvements before and during the upcoming Asian Games that will be hosted in Hangzhou in 2022.

Characteristics of PM_(2.5) and Its Reactive Oxygen Species in Heating Energy Transition and Estimation of Its Impact on the Environment and Health in China——A Case Study in the Fenwei Plain

To reduce the adverse effects of traditional domestic solid fuel,the central government began implementing a clean heating policy in northern China in 2017.Clean coal is an alternative low-cost fuel for rural households at the present stage.In this study,18 households that used lump coal,biomass,and clean coal as the main fuel were selected to evaluate the benefits of clean heating transformation in Tongchuan,an energy city in the Fenwei Plain,China.Both indoor and personal exposure(PE)samples of fine particulate matter(PM_(2.5))were synchronically collected.Compared with the lump coal and biomass groups,the indoor PM_(2.5)concentration in the clean coal group is 43.6%and 20.0%lower,respectively,while the values are 16.8%and 21.3%lower,respectively,in the personal exposure samples.PM_(2.5)-bound elements Cd,Ni,Zn,and Mn strongly correlated with reactive oxygen species(ROS)levels in all fuel groups,indicating that transition metals are the principal components to generate oxidative stress.Using a reliable estimation method,it is predicted that after the substitution of clean coal as a household fuel,the all-cause,cardiovascular,and respiratory disease that causes female deaths per year could be reduced by 16,6,and 3,respectively,in the lump coal group,and 22,8,and 3,respectively,in the biomass group.Even though the promotion of clean coal has led to impressive environmental and health benefits,the efficiencies are still limited.More environmental-friendly energy sources must be promoted in the rural regions of China.

Development and application of photocatalytic coating for roadside NO_(x) mitigation in Hong Kong

A facile chemical method for the development of photocatalytic coating products was proposed based on practical application perspective for the Hong Kong roadside nitrogen oxides(NO_(x))mitigation.TiO_(2)-based photocatalytic coating PC-C film with crystallized size of around 5–6 nm was synthesized with the peptization of H_(2)O_(2).The PC-C coating possesses a super-hydrophilicity surface and is proven to have a NO_(x)degradation rate of 46.8%with an optimum pH level of 7.In addition,the PC-C coating presents a promising photocatalytic NO_(x)degradation compared with other commercially available coating products and P25 when applied on two building materials of poly-methyl methacrylate(PMMA)and concrete surface.A weather resistance simulation and a 180-day on-site field trial were carried out the attenuation effects of photocatalytic coating applied in outdoor exposure.Based on epidemiological estimation and field investigation,hospital admissions for respiratory diseases(HARD)and mortality cases(MC)could be reduced with the application of PC-C coating along the street canyon.This work demonstrates the feasibility of air pollution control measures for the local roadside NO_(x)using photocatalytic technology,offering promising health benefits with environmental remediation.

Elaborations of the influencing factors on the formation of secondary inorganic aerosols in a heavily polluted urban area of China

In this study,online water-soluble inorganic ions were detected to deduce the formation mechanism of secondary inorganic aerosol in Xianyang,China during wintertime.The dominant inorganic ions of sulfate(SO_(4)^(2-)),nitrate(NO_(3)^(-)),and ammonium(NH_(4)^(+))(the sum of those is abbreviated as SNA)accounted for 17%,21%,and 12% of PM_(2.5)mass,respectively.While the air quality deteriorated from excellent to poor grades,the precursor gas sulfur dioxide(SO_(2))of SO_(4)^(2-)increased and then decreased with a fluctuation,while nitrogen dioxide(NO_(2))and ammonia(NH_(3)),precursors of NO_(3)^(-)and NH_(4)^(+),and SNA show increasing trends.Meteorological factors including boundary layer height(BLH),temperature,and wind speed also show decline trends,except relative humidity(RH).Meanwhile,the secondary conversion ratio shows a remarkable increasing trend,indicating that there was a strong secondary transformation.From the perspective of chemical mechanisms,RH is positively correlated with sulfur oxidation ratios(SOR),nitrogen oxidation ratios(NOR),and ammonia conversion ratios,representing that the increase of humidity could promote the generation of SNA.Notably,SOR and NOR were also positively related to the ammonia.On the one hand,the low wind speed and BLH led to the accumulation of pollutants.On the other hand,the increases of RH and ammonia promoted more formations of SNA and PM_(2.5).The results advance our identification of the contributors to the haze episodes and assist to establish more efficient emission controls in Xianyang,in addition to other cities with similar emission and geographical characteristics.

Growth of nitrate contribution to aerosol pollution during wintertime in Xi'an,northwest China:Formation mechanism and effects of NH_(3)

With the strengthened controls on SO2 emissions and extensive increases in motor vehicles'exhaust,aerosol pollution shifts from sulfate-rich to nitrate-rich in recent years in Xi'an,China.To further gain insights into the factors on nitrate formation and efficiently mitigate air pollution,highly time-resolved observations of water-soluble inorganic ions(WSIIs)in PM_(2.5) were measured in a suburban area of Xi'an,China during wintertime.Hourly concentration of total WSIIs is 39.8μg m-3 on average,accounting for 50.3%of PM_(2.5) mass.In contrast to a slight decrease in the mass fraction of SO42-,NO_(3)-shows a sig-nificant increase of the PM_(2.5) contribution with the aggravation of aerosol pollution.This suggests the importance of NO_(3)-formation to haze evolution.Furthermore,homogeneous reactions govern the formation of NO_(3)-,while alkali metals such as calcium and sodium play an additional role in retaining NO_(3)-in PM_(2.5) during clean periods.However,the heterogeneous hydrolysis reaction contributed more to NO_(3)-formation during the pollution periods under high relative humidity.Our investigation reveals that temperature,relative humidity,oxidant,and ammonia emissions facilitate rapid NO_(3)-formation.Using the random forest(RF)model,NO_(3)-concentrations were successfully simulated with measured variables for the training and testing datasets(R2>0.95).Among these variables,CO,NH_(3),and N02 were found to be the main factors affecting the NO_(3)-concentrations.Compared with the period without vehicle re-striction,the contributions of NO_(3)-and NH4+to PM_(2.5) mass decreased by 5.3%and 3.4%in traffic re-striction periods,respectively.The vehicle restriction leads to the decreases of precursor gases of NO2,SO2,and NH_(3) by 12.8%,5.9%,and 27.6%,respectively.The results demonstrate collaborative emission reduction of NOx and NH_(3) by vehicle restrictions,and using new energy vehicles(or electric vehicles)can effectively alleviate particulate matter pollution in northwest China.

Surrogate atmospheric dust particles generated from dune soils in laboratory: Comparison with field measurement

Desert dust strongly influences the climate and the environment by altering the radiation budget, participating in atmospheric chemical reactions, and engaging the biogeochemical cycle. Studying its impacts requires knowledge of the physical and chemical properties of the original particles from the source origin. Unfortunately, the field collection of atmospheric samples in the desert is impractical. Fine surface soil is thus considered an alternative material from which to obtain the information applicable to dust particles from the desert soil. In this study, a laboratory system was set up to generate dust particles with simulated natural wind erosion processes from surface soils or directly from desert surfaces. Surface soils and field dust were simultaneously collected during a local blowing dust event. The comparison between the laboratory-generated dust and the field dust showed a consistent trend in particle size distribution and chemical composition. The chemical compositions were found to have explainable differences with the Certified Reference Materials for Asian dust (CJ-2). The laboratory-generated dust particles with the system could be applied as surrogates for soil-emitted dust in desert areas.

PM_(2.5)-bound polycyclic aromatic hydrocarbons(PAHs) in Beijing:Seasonal variations,sources,and risk assessment

Polycyclic aromatic hydrocarbons(PAHs) have been of health concern due to its carcinogenesis and mutagenesis. In this study, we aimed to assess the variations, sources, and lifetime excessive cancer risk(ECR) attributable to PAHs bound to ambient particulate matters with aerodynamic diameter less than 2.5 μm(PM_(2.5)) in metropolitan Beijing, China. We collected24-hour integrated PM_(2.5) samples on daily basis between November 2014 and June 2015 across both central heating(cold months) and non-heating(warm months) seasons, and further analyzed the PAH components in these daily PM_(2.5) samples. Our results showed that total concentrations of PM_(2.5)-bound PAHs varied between(88.6 ± 75.4) ng/m^3 in the cold months and(11.0 ± 5.9) ng/m^3 in the warm months. Benzo[a]pyrene(Ba P), the carcinogenic marker of PAHs,averaged at 5.7 and 0.4 ng/m^3 in the cold and warm months, respectively. Source apportionment analyses illustrated that gasoline, biomass burning, diesel, coal combustion and cooking were the major contributors, accounting for 12.9%, 17.8%, 24.7%, 24.3% and 6.4% of PM_(2.5)-bound PAHs, respectively. The BaP equivalent lifetime ECR from inhalation of PM_(2.5)-bound PAHs was 16.2 cases per million habitants. Our results suggested that ambient particulate reduction from energy reconstruction and adaption of clean fuels would result in reductions PM_(2.5)-bound PAHs and its associated cancer risks. However, as only particulate phased PAHs was analyzed in the present study, the concentration of ambient PAHs could be underestimated.