Reduction Of Volatile Organic Compounds Research Articles

Impact of spatial scales of control measures on the effectiveness of ozone pollution mitigation in eastern China

Ozone (O3) pollution is becoming the primary air pollution issue with the large decrease in fine particulate concentrations in eastern China. The development of widely recognized policies for controlling O3 pollution episodes is urgent. This study aims to provide actionable and comprehensive suggestions for O3 control policy development, with an emphasis on the precursor emission reductions.Here, we compared the impacts of different spatial scale reductions on a widespread O3 pollution episode in eastern China by a state-of-the-art regional air quality model. We find that region-scale joint control (in >30 cities) is much more effective than city-scale sporadic reduction in reducing O3 concentration. Sporadic controls only reduce the maximum daily 8-h average (MDA8) O3 by ∼1 μg/m3 in the controlled city, whereas regional controls lead to a MDA8 O3 decrease of ∼8 μg/m3 in the controlled region. In addition, the emission reduction effectiveness increased by 2.6 times from <5 cities to >30 cities. Continuous reductions have a cumulative effect on the decrease of MDA8 O3, showing the strongest effects within 24 h and diminishing after 48 h, which underscores the importance of reducing emissions 24 h prior to an episode. Moreover, the effect of control measures on MDA8 O3 varies spatially depending on the ratio of volatile organic compounds (VOCs) to nitrogen oxides (NOx) (VOCs/NOx). Both the reductions of VOC and NOx emissions have a positive effect on the decrease of MDA8 O3 in summer, but the effects of VOC reductions are 1.2 to 1.7 times higher than those of NOx reductions. The residential sector, due to its high VOCs/NOx emission ratio, exhibits the highest efficiency in the reduction of O3 concentrations. Our results highlight the importance of regional joint control and synergistic reduction of VOCs and NOx in eastern China.

Historical emission and reduction of VOCs from the petroleum refining industry and their potential for secondary pollution formation in Guangdong, China

China became the world leader in crude oil processing capacity in 2021. However, petroleum refining generates significant volatile organic compound (VOC) emissions, and the composite source profile, source-specific emission factors, and emission inventories of VOCs in the petroleum refining industry remain poorly understood. In this study, we focused on Guangdong, China's major province for crude oil processing, and systematically evaluated the historical emissions and reduction of VOCs in the petroleum refining industry from 2001 to 2020. We accomplished this by establishing local source-specific emission factors and composite source profiles. Finally, we quantitatively assessed the potential impact of these emissions on ozone and secondary organic aerosol formation. Our results revealed that VOC emissions from the petroleum refining industry in Guangdong followed an increasing-then-decreasing trend from 2001 to 2020, peaking at 37.3 Gg in 2016 and declining to 18.7 Gg in 2020. Storage tanks and wastewater collection and treatment remained the two largest sources, accounting for 41.9 %–53.4 % and 20.6 %–27.5 % of total emissions, respectively. Initially, Guangzhou and Maoming made the most significant contributions, with Huizhou becoming a notable contributor after 2008. Emission reduction efforts for VOCs in Guangdong's petroleum refining industry began showing results in 2017, with an average annual VOC emission reduction of 21.5 Gg from 2017 to 2020 compared to the unabated scenario. Storage tanks, wastewater collection and treatment, and loading operations were the primary sources of emission reduction, with significant contributions from Maoming, Huizhou, and Guangzhou. Alkanes made the largest contribution to VOC emissions, while alkenes/alkynes and aromatics comprised the most significant portions of ozone formation potential (OFP) and secondary organic aerosol formation potential (SOAP). We also estimated VOC emissions and reduction from petroleum refining for China from 2001 to 2020, and measures such as “one enterprise, one policy” and deep control strategies could reduce emissions by at least 103.9 Gg.

Source apportionment of anthropogenic and biogenic organic aerosol over the Tokyo metropolitan area from forward and receptor models

Organic aerosol (OA) is a dominant component of PM2.5, and accurate knowledge of its sources is critical for identification of cost-effective measures to reduce PM2.5. For accurate source apportionment of OA, we conducted field measurements of organic tracers at three sites (one urban, one suburban, and one forest) in the Tokyo Metropolitan Area and numerical simulations of forward and receptor models. We estimated the source contributions of OA by calculating three receptor models (positive matrix factorization, chemical mass balance, and secondary organic aerosol (SOA)-tracer method) using the ambient concentrations, source profiles, and production yields of OA tracers. Sensitivity simulations of the forward model (chemical transport model) for precursor emissions and SOA formation pathways were conducted. Cross-validation between the receptor and forward models demonstrated that biogenic and anthropogenic SOA were better reproduced by the forward model with updated modules for emissions of biogenic volatile organic compounds (VOC) and for SOA formation from biogenic VOC and intermediate-volatility organic compounds than by the default setup. The source contributions estimated by the forward model generally agreed with those of the receptor models for the major OA sources: mobile sources, biomass combustion, biogenic SOA, and anthropogenic SOA. The contributions of anthropogenic SOA, which are the main focus of this study, were estimated by the forward and receptor models to have been between 9 % and 15 % in summer 2019. The observed percent modern carbon data indicate that the amounts of anthropogenic SOA produced during daytime have substantially declined from 2007 to 2019. This trend is consistent with the decreasing trend of anthropogenic VOC, suggesting that reduction of anthropogenic VOC has been effective in reducing anthropogenic SOA in the atmosphere.

Environmental hazard reduction and anti-aging enhancement of steel slag powder-asphalt mastic based on TiO2@UiO-67 composites

Steel slag asphalt pavements (SAPs) will deteriorate during the production and service process, bringing heavy metal ions leaching contamination and irregular release of Volatile Organic Compounds (VOCs), which pose great challenges to maintenance and ecological environment. TiO2@UiO-67 composites were synthesized, their basic physical-chemical properties were investigated, and they were applied to SAPs to prepare an eco-friendly steel slag powder-asphalt mastic (ESAM) with multiple effects of anti-aging, heavy metal ions reduction, and VOCs emission inhibition. The rheological behavior of ESAM was explored, and the anti-aging, heavy metal inhibition, and VOCs reduction mechanism was investigated. The results showed that TiO2@UiO-67 composites with excellent properties such as large surface area, high activity and stability, powerful adsorption ability, controlled structure, and specific functional group/targeted adsorption were prepared. Some terminal hydroxyl groups were reacted with reactive radicals to prevent the growth of asphalt chain segments by reducing the aging of asphalt. The binding energy and adsorption between UiO-67 with heavy metal ions and VOCs were simulated by Materials Studio (MS), and the results showed that the recovery of Cr (VI) was up to 57.7% and the reaction proceeded spontaneously. In addition, the conjugated system, the molecular size and the spatial site resistance synergistically reduced Category 1 carcinogens by up to 85.6%, ultimately reducing the total emission concentration of VOCs by 65.4%. It provides theoretical guidance for the application of TiO2@UiO-67 composites in SAPs, and technical feasibility for anti-aging, and pollutant emission reduction strategies for SAPs.

The role of NOx in Co-occurrence of O3 and PM2.5 pollution driven by wintertime east Asian monsoon in Hainan

Clarifying the driving forces of O3 and fine particulate matter (PM2.5) co-pollution is important to perform their synergistic control. This work investigated the co-pollution of O3 and PM2.5 in Hainan Province using an observation-based model and explainable machine learning. The O3 and PM2.5 pollution that occurs in winter is affected by the wintertime East Asian Monsoon. The O3 formation shifts from a NOx-limited regime with a low O3 production rate (PO3) in the non-pollution season to a transition regime with a high PO3 in the pollution season due to an increase in NOx concentrations. Increased O3 and atmospheric oxidation capacity promote the conversion from gas-phase precursors to aerosols. Meanwhile, the high concentration of particulate nitrate favors HONO formation via photolysis, in turn facilitating O3 production. Machine learning reveals that NOx promotes O3 and PM2.5 co-pollution during the pollution period. The PO3 shows an upward trend at the observation site from 2018 to 2022 due to the inappropriate reduction of volatile organic compounds (VOCs) and NOx in the upwind areas. Our results suggest that a deep reduction of NOx should benefit both O3 and PM2.5 pollution control in Hainan and bring new insights into improving air quality in other regions of China in the future.

A Comparison of the Evaporative Emissions Performance of Light-Duty Vehicles under US Tier 3 and China 6 Test Conditions

To further improve air quality in China, especially ozone and fine particulate matter (PM2.5), additional reductions of volatile organic compounds (VOCs) are needed. Evaporative emissions from internal combustion engines (ICE) and hybrid vehicles are known to be an important source of VOCs in urban cities, which can be efficiently reduced through the introduction of more stringent regulatory standards. The most stringent global standards for evaporative emissions are the U.S. Tier 3 light-duty vehicle standards. This study compares the evaporative emissions of light-duty ICE vehicles designed to China 6 and U.S. Tier 3 regulations for both China and U.S. test conditions. Data are analyzed from manufacturer testing of full vehicle evaporative emissions conducted in the laboratory following U.S. Tier 3 and China 6 certification test methods utilizing Sealed Housing for Evaporative Determination (SHED) chambers equipped with Flame Ionization Detection (FID) analyzers. Vehicles designed to U.S. Tier 3 standards are observed to have 64% lower diurnal and hot soak evaporative emissions and 98% lower canister bleed emissions relative to vehicles designed to China 6 standards. U.S. Tier 3, U.S. Tier 2, and China 6 light-duty evaporative emission certification values submitted by manufacturers are also compared. The average of all current U.S. Tier 3 certifications is, on average, 52.4% lower than the average of all China 6 certifications. The results from the testing and data analysis of five vehicles, with comparison to the certification data, suggest that the introduction of standards equivalent in stringency to U.S. Tier 3 in China can significantly reduce evaporative emissions relative to China 6.

VOC Emission from Lightweight Wood Fiber Insulation Board

The aim of the presented research work was to determine and analyze emissions of volatile organic compounds (VOCs) from experimental lightweight wood fiber insulation board produced in dry technology. Until now, there have been no rigid insulation materials made of wood fibers produced in such low density and made in dry technology. Among the typical parameters such as thermal conductivity and the mechanical performance of the lightweight board, attention was also paid to their influence on indoor air quality. Therefore, an attempt was made to determine the kind of substances emitting from wood fiber insulation boards produced at defined production parameters as well as the dynamics of emission reduction over time. Additionally, the influence of fire retardants used for protection against lightweight wood fiberboard fires on the emission of VOCs was analyzed. Tests on VOC emissions were carried out using the chamber method according to the applicable ISO 16000 standards. The main components emitting from lightweight insulation fiberboards were acetic acid and aldehydes such as pentanal, hexanal, heptanal, octanal, nonanal, decanal, furfural, and benzaldehyde. The percentage of acetic acid in total volatile organic compounds (TVOCs) was within the limits of 17% to 65%. From the aldehydes group, the most concerning substance was furfural due to a very strict limit value. In the presented research, depending on the variant, the emission of furfural was from 0 up to 10 µg/m3 after 28 days of measurement. Other substances such as terpenes or aromatic hydrocarbons were at a very low level. The reduction in VOCs over a period of 28 days was significant in most cases from 22% up to 61%. The tests carried out also showed a substantial impact of fire retardant, used in the production of lightweight insulation fiberboard, on the emission of VOCs from fiberboards, and thus on their quality.

A WRF-CMAQ modeling of atmospheric peroxyacetyl nitrate and source apportionment in Central China

Atmospheric peroxyacetyl nitrate (PAN), as an essential constituent in the photochemical smog, is formed from photochemical reactions between volatile organic compounds (VOCs) and NOx. However, limited regional studies on distribution, formation and sources of PAN restrict the further understanding of the atmospheric behavior and environmental significance of PAN. In this study, the variation characteristics of PAN and the influencing factors to PAN concentrations were investigated using the WRF-CMAQ model simulation in the central China during July 2019. The results showed that the monthly mean concentration of PAN in the near-surface layer was 0.4 ppbv and increased with the height rising, accompanied by strong intra-day variation. The process analysis suggested that the removal was mainly controlled by dry deposition (57 %), followed by the gas-phase chemistry (43 %) which was mainly attributed to the thermal decomposition. Based on the sensitivity simulation, PAN concentrations decreased effectively in most of the simulated regions when precursors of VOCs and NOx emissions were reduced, and PAN concentrations were more sensitive to VOCs emissions than NOx emissions. The reduction of NOx and VOCs could lead to enhanced atmospheric oxidation in east-central region, which in turn hindered the decrease of PAN concentrations. During the simulation period, we found that emissions from industry and transportation sectors had the greatest impact on PAN concentrations in the central China, with contributions of 39 %–49 % and 33 %–41 %, respectively.

Ozone Pollution Characteristics and Sensitivity During the Ozone Pollution Days in Summer 2021 of Xinxiang City

This study was based on the observation of volatile organic compounds (VOCs), conventional gaseous air pollutants, and meteorological parameters observed at the Xinxiang Municipal Party School site from June to August 2021. The ozone (O3) characteristics and sensitivity of O3 pollution days and the control strategy of its precursors were studied using an observation-based model (OBM). It was found that the meteorological conditions were characterized by high temperature, low humidity, and low pressure in O3-pollution days. The concentrations of O3 and its precursors all increased in the O3 pollution days. Oxygenated volatile organic compounds (OVOCs) and alkanes were the highest-concentration components of VOCs on O3 pollution days in Xinxiang, and OVOCs had the highest ozone formation potential (OFP) and hydroxyl (·OH) reactivity. According to the relative incremental reactivity (RIR) analysis, during the O3 pollution days in Xinxiang, O3sensitivity was in the VOCs-limited regime in June and in the transitional regime in July and August. Ozone production was more sensitive to alkenes and OVOCs. The RIR values of the precursors in June changed throughout the day, but O3 sensitivity remained the VOCs-limited regime. In July and August, O3 sensitivity was the VOCs-limited regime in the morning, transitional regime at noon, transitional and NOx-limited regime, respectively in the afternoon. By simulating different precursor-reduction scenarios, the results showed that the reduction of VOCs was always beneficial to the control of O3, whereas the reduction of NOx had little effect on the control of O3 and a risk of increasing O3.

The Effects of an Advanced Air Purification Technology on Environmental and Clinical Outcomes in a Long-Term Care Facility.

Long-term care facilities (LTCFs) are constantly working to reduce sources of infectious pathogens to improve resident care. LTCF residents are particularly susceptible to health care-associated infections (HAIs), many of which originate from the air. An advanced air purification technology (AAPT) was designed to comprehensively remediate volatile organic compounds (VOCs) and all airborne pathogens including all airborne bacteria, fungi, and viruses. The AAPT contains a unique combination of proprietary filter media, high-dose ultraviolet germicidal irradiation, and high-efficiency particulate air (HEPA) filtration. The AAPT was installed in an LTCF's heating, ventilation, and air-conditioning ductwork and 2 floors were studied: the study floor with comprehensive AAPT remediation and HEPA filtration and the control floor with only HEPA filtration. VOC loading and airborne and surface pathogen loading were measured in 5 locations on both floors. Clinical metrics such as HAI rates were also studied. There was a statistically significant 98.83% reduction in airborne pathogens, which are responsible for illness and infection, an 89.88% reduction in VOCs, and a 39.6% reduction in HAIs. Surface pathogen loading was reduced in all locations except 1 resident room where the detected pathogens were linked to direct touch. The removal of airborne and surface pathogens by the AAPT led to a dramatic reduction in HAIs. The comprehensive removal of airborne contaminants has a direct positive impact on resident wellness and quality of life. It is critical that LTCFs incorporate aggressive airborne purification methods with their current infection control protocols.

Investigation of Summertime Ozone Formation and Sources of Volatile Organic Compounds in the Suburb Area of Hefei: A Case Study of 2020

Ground surface ozone (O3) is an emerging concern in China due to its complex formation process. In August 2020, field measurements of O3, NOx, and volatile organic compounds (VOCs) were carried out in Hefei’s western suburbs. The pollution features of VOCs and O3 formation were thoroughly analyzed. The total VOC concentration was 42.26 ppb, with the dominant contributor being oxygenated VOCs (OVOCs). Seven emission sources were recognized using the positive matrix factorization (PMF) model, including aged air masses, combustion sources, fuel evaporation, industrial emissions, vehicular emission, solvent utilization, and biogenic emission. Ozone generation mainly occurred under an NOx-limited regime based on the zero-dimensional box model analysis. According to the scenario analysis, the 13% cut in O3 might be achieved by the 10% and 30% reduction in NOx and VOCs, respectively. The O3 budget analysis demonstrates its high ozone production rate during the pollution period. The influence of regional transport cannot be ignored for high O3 pollution. This paper provides scientific evidence for O3 production and the strategies of reducing O3 by controlling its precursors.

Characterizing sources and ozone formations of summertime volatile organic compounds observed in a medium-sized city in Yangtze River Delta region

Volatile organic compounds (VOCs) emitted from various sources into atmosphere could cause serious O3 pollution in urban areas. Although characterizations of ambient VOCs have been extensively studied in megacities, they are scarcely investigated in medium/small-sized cities, which could present different pollution characterizations due to the factors like emission sources and populations. Herein, field campaigns were conducted concurrently at six sites in a medium-sized city of Yangtze River Delta region to determine ambient levels, O3 formations and source contributions of summertime VOCs. During the observation period, the total VOC (TVOCs) mixing ratios ranged from 27.10 ± 3.35 to 39.09 ± 10.84 ppb at six sites. The ozone formation potential (OFP) results showed that alkenes, aromatics and oxygenated VOCs (OVOCs) were dominant contributors, together sharing 81.4% of total calculated OFPs. Ethene ranked the largest OFP contributor at all six sites. A high VOC site, KC, was selected as a case to detailed analyze diurnal variations of VOCs and its relationship with O3. Consequently, diurnal patterns varied with VOC groups, and TVOC concentrations were lowest during strong photochemical period (15:00–18:00 p.m.), opposite to the O3 peak. VOCs/NOx ratios and observation-based model (OBM) analysis revealed that O3 formation sensitivity was primarily in transition regime in summertime and that the reduction of VOCs rather than NOX would be more efficient to suppress O3 peak at KC during pollution episode. Additionally, source apportionment conducted with positive matrix factorization (PMF) indicated that industrial emission (29.2%–51.7%) and gasoline exhaust (22.4%–41.1%) were major sources for VOCs at all six sites, and that VOCs from industrial emissions and gasoline exhaust were the key precursors for ozone formation. Our results shed light on the importance of alkenes, aromatics and OVOCs in forming O3 and propose that preferentially reducing VOCs especially those from industrial emission and gasoline exhaust would benefit alleviating O3 pollution.

Tracing the origin of VOCs in post-consumer plastic film bales

Volatile organic compounds (VOCs), including odors, are still a key issue in plastic recycling, especially in case of flexible packaging. Therefore, this study presents a detailed qualitative and quantitative VOC analysis by applying gas chromatography on 17 categories of flexible plastic packaging that are manually sorted from bales of post-consumer flexible packaging (e.g., beverage shrink wrap, packaging for frozen food, packaging for dairy products, etc.). A total of 203 VOCs are identified on packaging used for food products, while only 142 VOCs are identified on packaging used for non-food products. Especially, more oxygenated compounds (e.g., fatty acids, esters, aldehydes) are identified on food packaging. With more than 65 VOCs, the highest number of VOCs is identified on packaging used for chilled convenience food and ready meals. The total concentration of 21 selected VOCs was also higher on packaging used for food products (totally 9187 μg/kg plastic) compared to packaging used for non-food packaging (totally 3741 μg/kg plastic). Hence, advanced sorting of household plastic packaging waste, e.g., via tracer-based sorting or watermarking, could open the door towards sorting on other properties than polymer type, such as mono- versus multi-material packaging, food versus non-food packaging or even their VOC profile, which might allow for tailoring washing procedures. Potential scenarios showed that sorting the categories with the lowest VOC load, which corresponds to half of the total mass of flexible packaging, could result in a VOC reduction of 56%. By producing less contaminated plastic film fractions and by tailoring washing processes recycled plastics can ultimately be used in a broader market segment.

VOC Emission Characteristics of the Glass Deep-Processing Industry in China

To understand the pollution characteristics of volatile organic compounds (VOCs) in the glass deep-processing industry, samples were collected using polyvinyl fluoride bags and quickly transferred to summa tanks for GC/MS/FID analysis. The emission characteristics of VOCs, the ozone formation potential and the secondary aerosol formation potential were studied. The results showed that the VOCs emitted by the six enterprises were mainly aromatics and OVOCs, accounting for 35% to 97% of the emissions, with high emission loads of alkanes and halocarbons from individual enterprises. The stack emissions from Enterprise 2 were as high as 38 mg/m3, while the emissions from the remaining five enterprises were all in the range of 1.7~4.1 mg/m3, probably because the terminal treatment facilities were not updated in a timely manner, resulting in excessive stack emissions from Enterprise 2. The characteristic pollutants, including OVOCs, aromatics and alkanes, which are mainly derived from spray painting and gluing, were screened in the six enterprises. Aromatics and OVOCs contributed the most to the ozone formation potential in the six enterprises, with some enterprises having a high contribution from alkanes and alkenes. On the basis of the secondary aerosol formation potential, toluene, benzene, ethylbenzene, o-xylene and m/p-xylene account for 98% of the six enterprises’ emissions. Glass enterprises should prioritise the control of benzene and OVOCs emissions. The glass processing industry mainly emits aromatics, OVOCs and alkanes. Through a preliminary study on the emission characteristics of VOCs in the glass deep-processing industry, we provided basic data for the reduction and control of VOCs in the glass deep-processing industry in China.

Controlled air exchange rate method to evaluate reduction of volatile organic compounds by indoor air cleaners

Air cleaning technologies are needed to reduce indoor concentrations and exposure to volatile organic compounds (VOCs). Currently, air cleaning technologies lack an accepted test standard to evaluate their VOC removal performance. A protocol to evaluate the VOC removal performance of air cleaning devices was developed and piloted with two devices. This method injects a VOC mixture and carbon dioxide into a test chamber, supplies outdoor air at a standard building ventilation rate, periodically measures the VOC concentrations in the chamber using solid phase microextraction-gas chromatography-mass spectrometry over a 3-h decay period, and compares the decay rate of VOCs to carbon dioxide to measure the VOC removal air cleaning performance. The method was demonstrated with both a hydroxyl radical generator and an activated carbon air cleaner. It was shown that the activated carbon air cleaner device tested had a clean air delivery rate an order of magnitude greater than the hydroxyl radical generator device (72.10 vs 6.32 m3/h).

A Peripherally Located Air Recirculation Device Containing an Activated Carbon Filter Reduces VOC Levels in a Simulated Operating Room.

Electrosurgery procedures produce airborne contaminants including volatile organic compounds (VOCs). The effectiveness of commercial grade activated carbon at removing toluene, a typical VOC, from the air in an enclosed simulated operating room (OR) when interfaced with an air recirculation device was tested. The concentration of toluene in the air was measured using gas sensitive semiconductor VOC sensors. When the air recirculation device containing activated carbon was turned on, the concentration of toluene in the air decayed exponentially. When the device was off, the toluene concentration reduced much more slowly. After 130 min, a VOC sensor placed near the air recirculation device showed VOC reductions of approximately 30% when the device is on and less than 1% when the device is off. Changing the activated carbon filter after 22 h of constant use showed an abrupt increase in the rate of toluene removal.

Investigation into the differences and relationships between gasSOA and aqSOA in winter haze pollution on Chongming Island, Shanghai, based on VOCs observation

To investigate the formation of secondary organic aerosol (SOA) under current atmospheric conditions, we conducted a field observation of SOA precursors in the downwind region of the Yangtze River Delta (YRD) in winter 2019 using a variety of offline and online instruments. During the entire observation period, the averaged fine particulate SOA was 7.9 ± 2.3 μg m−3, with precursor concentrations of 31 ± 11 ppbv for the measured volatile organic compounds (VOCs) and 16 ± 12 ppbv for NOx. Compared to those on the clean days, SOA on the haze days increased by a factor of 1.6, while the VOC and NOx increased by a factor of 1.3 and 2.0, respectively. Aerosol liquid water content (ALWC) and oxygenated VOCs (OVOCs, including acetaldehyde, formic acid, acetone, acetic acid, methyl ethyl ketone, and methylglyoxal) relationships suggested that the gasSOA and aqSOA occurred simultaneously on Chongming Island in winter. The gasSOA was primarily formed by the oxidation of aromatics and NOx at low RH (RH < 80%) conditions. In contrast, the aqSOA was formed under higher RH (RH > 80%) conditions via a combination of daytime photochemical aqueous phase processes of water-soluble OVOCs and nocturnal dark aqueous phase processes of primary emissions from biomass. The inversed higher mass ratio of NACs to (benzene + toluene) and nitrogen oxidation ratio (NOR) in the daytime during the gasSOA-dominated haze periods indicated that gasSOA could be transformed to aqSOA at high NOx levels. Our results also suggested the importance of NOx and VOC reduction measures in directly mitigating gasSOA and indirectly mitigating aqSOA during winter haze pollution.

Investigation of O3-precursor relationship nearby oil fields of Shandong, China

Oil exploitation can release a large amount of volatile organic compounds (VOCs), which play an important role in tropospheric chemistry and contribute to ozone (O3) and secondary organic aerosols (SOA) formation in its surrounding environment. To evaluate the impact of oil exploitation on tropospheric O3 formation, a comprehensive field campaign on O3 and its precursors (VOC, NOx, etc) was conducted during May–September 2019 in a site nearby oil fields of Shandong province, China. The average mixing ratio of the total VOC (TVOC) was 59.2 ± 30.2 ppbv, and alkanes contributed 78% of TVOC (with C2–C5 alkanes as the main contributors). A 0-D box model incorporating the latest Master Chemical Mechanism (MCMv3.3.1) was applied using observations as constraints, and we found that the O3 formation was mainly under transitional and VOC-limited regime for high-O3 and low-O3 periods, respectively. The relative incremental reactivity (RIR) values from individual AVOC species were basically consistent with those calculated from OH reactivity, and both metrics suggested that C3–C5 alkanes, C2–C5 alkenes, and C7–C9 aromatics were the most sensitive VOC species to O3 formation. The results from empirical kinetic modeling approach (EKMA) indicated large day-to-day variations of photochemical regimes, which covered VOC-limited, transitional, and NOx-limited regimes on a daily basis during the five-month campaign. The emission reduction modeling with a large number of scenarios further suggested that the reduction of anthropogenic VOC and NOx at a ratio of 1:3 would be a more practical strategy for mitigation of the local O3 pollution. These results could provide a basis for understanding the O3-precursor relationship nearby the oil field area, and the derived policy-relevant emission control strategy could provide guidance for other oil field in Shandong and other regions to take effective O3 control measures.

Fast near-surface ClNO2 production and its impact on O3 formation during a heavy pollution event in South China

Atmospheric nitryl chloride (ClNO2) acts as a reservoir of both NOx and reactive chlorine radicals and therefore affects atmospheric oxidation chemistry and the production of secondary pollutants such as ozone (O3). However, the factors contributing to ClNO2 production and its impact on O3 formation in the polluted atmosphere are not fully understood. Here, we investigated the causes and impacts of extremely high ClNO2 levels (up to 8.3 ppbv, 1 min average) in a winter pollution episode at a semi-rural surface site in South China. Anthropogenic activities (mainly coal burning) produced an abundant amount of chloride, and high NO3 production rates and efficient N2O5 uptake by aerosols facilitated ClNO2 production at night. We used a chemical box model to assess the ClNO2 impact on next-day O3 production both at the site and in downwind areas. The model results showed that ClNO2 chemistry led to 6.6 % enhancement of net Ox (=NO2 + O3) production at the site, while the enhancement was increased to 11.2 % in the air mass transporting downwind, which resulted in 20 ppbv (38.5 % max) increment of peak O3 concentration. ClNO2 also changed the response of O3 to reduction in the concentration of O3 precursors (NOx and anthropogenic volatile organic compounds (VOCs)), thereby affecting the design of NOx and VOC reduction strategies for O3 pollution mitigation. Reducing chloride emissions can help alleviate the emission reduction burden for NOx and anthropogenic VOCs.

A Study of Ventilation Effects Expected to Reduce Harmful Substances Generated during Manicure Procedures

This study attempted to improve working environments for nail salon employees and expand their awareness of hazardous materials. Specifically, it measured and analyzed volatile organic compounds (VOCs) produced during manicure procedures using a direct-reading instrument and devised a plan to minimize exposure to such hazardous substances. For this, the emissions of 3 VOCs (formaldehyde, toluene, and acetone) were tested on one foreign and two domestic manicure products, using GASTEC GV-100. In terms of the reduction of VOCs emissions, they were measured and comparatively analyzed through 2 different methods, spontaneous disappearing over time and natural ventilation by opening a chamber, and the results found the following: The product manufactured by ‘C’ revealed high VOCs emissions. In particular, ‘acetone’ was the highest. However, the spontaneous reduction of VOCs over time was minor. In other words, direct reduction, such as ventilation instead of spontaneous disappearing, is necessary. The above results confirm that ventilation is crucial in nail salons.