An uncertainty for clean air: Air quality modeling implications of underestimating VOC emissions in urban inventories

Zhu, Shupeng; Kinnon, Michael Mac; Shaffer, Brendan; Samuelsen, G. S.; Brouwer, Jacob; Dabdub, Donald

doi:10.1016/j.atmosenv.2019.05.019

Cited by 24 publications

(14 citation statements)

References 115 publications

(114 reference statements)

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“…This suggests that there is interannual variability most likely from wildfires but also a significant contribution from primary sources in the winter and secondary sources in the summer. The temporal profiles suggest that the winter primary source is residential wood burning, in agreement with measurements (Betha et al, 2018), and that the summer is strongly influenced by secondary organic aerosols, in agreement with modeling studies (Zhu et al, 2019). Figure 10 shows the annual trends and weekday patterns of ammonium nitrate and ammonium sulfate.…”

Section: Pm 25 Speciation Trendssupporting

confidence: 86%

“…As a result, emissions of volatile organic compounds are thought to be underestimated in the San Joaquin Valley. Modeling studies suggest that updating the emissions would lead to increased reactivity in the winter atmosphere leading to increased formation of ammonium nitrate (Zhu et al, 2019). Measurements and modeling for the Salt Lake Valley suggest that reducing volatile organic compounds may therefore be more effective at reducing ammonium nitrate concentrations than reducing NO x mole fractions (Womack et al, 2019).…”

Section: Research Articlementioning

confidence: 99%

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Changes in speciated PM2.5 concentrations in Fresno, California, due to NOx reductions and variations in diurnal emission profiles by day of week

Foy

Schauer

2019

Elementa: Science of the Anthropocene

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The San Joaquin Valley in California suffers from poor air quality due to a combination of local emissions and weak ventilation. Over the course of decades, there has been a concerted effort to control emissions from vehicles as well as from residential wood burning. A multiple linear regression model was used to evaluate the trends in air pollution over multiple time scales: by year, by season, by day of the week and by time of day. The model was applied to 18 years of measurements in Fresno including hourly mole fractions of NOx and concentrations of PM2.5; and daily measurements of speciated components of PM2.5. The analysis shows that there have been reductions in NOx, elemental carbon and ammonium nitrate of 4 to 6%/year. On weekends, NOx mole fractions are reduced by 15 to 30% due to fewer vehicle miles traveled and a smaller fraction of diesel traffic. These weekend reductions in NOx have not been accompanied by weekend reductions in PM2.5 however. In particular, elemental and organic carbon concentrations are higher on winter weekends. Analysis of diurnal profiles suggests that this is because of increased PM2.5 on Saturday and holiday evenings which are likely due to residential wood combustion. Furthermore, while organic carbon concentrations have decreased in the winter months, they have been variable but without a net decline in the summer, most likely as a result of forest fires offsetting other improvements in air quality. Fog was found to greatly enhance ammonium nitrate formation and was therefore associated with higher PM2.5 in the winter months. Overall the analysis shows that air quality controls have been effective at reducing NOx all year and PM2.5 in the winter, that continued reductions in emissions will further reduce pollutant concentrations, but that winter residential wood combustion and summer forest fires could offset some of the gains obtained.

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Section: Pm 25 Speciation Trendssupporting

confidence: 86%

Section: Research Articlementioning

confidence: 99%

Changes in speciated PM2.5 concentrations in Fresno, California, due to NOx reductions and variations in diurnal emission profiles by day of week

Foy

Schauer

2019

Elementa: Science of the Anthropocene

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“…Third, VCPs feature substantial quantities of intermediate-volatility organic carbon (IVOC) compounds ( CARB, 2019 ), and better representing their source strength could help resolve the high IVOC concentrations observed in urban atmospheres ( Lu et al, 2020 ; Zhao et al, 2014 ). Fourth, if the VCP sector is systematically biased low in the NEI or select urban areas, there could be implications for ozone pollution ( Zhu et al, 2019 ). Finally, reducing organic emissions from VCPs has traditionally been viewed through the lens of minimizing near-field chemical exposure ( Isaacs et al, 2014 ) or mitigating ozone pollution ( Ozone Transport Commission, 2018 ), both of which can be accomplished through product reformulation.…”

Section: Introductionmentioning

confidence: 99%

Reactive organic carbon emissions from volatile chemical products

et al. 2021

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Abstract. Volatile chemical products (VCPs) are an increasingly important source of anthropogenic reactive organic carbon (ROC) emissions. Among these sources are everyday items, such as personal care products, general cleaners, architectural coatings, pesticides, adhesives, and printing inks. Here, we develop VCPy, a new framework to model organic emissions from VCPs throughout the United States, including spatial allocation to regional and local scales. Evaporation of a species from a VCP mixture in the VCPy framework is a function of the compound-specific physiochemical properties that govern volatilization and the timescale relevant for product evaporation. We introduce two terms to describe these processes: evaporation timescale and use timescale. Using this framework, predicted national per capita organic emissions from VCPs are 9.5 kg per person per year (6.4 kg C per person per year) for 2016, which translates to 3.05 Tg (2.06 Tg C), making VCPs a dominant source of anthropogenic organic emissions in the United States. Uncertainty associated with this framework and sensitivity to select parameters were characterized through Monte Carlo analysis, resulting in a 95 % confidence interval of national VCP emissions for 2016 of 2.61–3.53 Tg (1.76–2.38 Tg C). This nationwide total is broadly consistent with the U.S. EPA's 2017 National Emission Inventory (NEI); however, county-level and categorical estimates can differ substantially from NEI values. VCPy predicts higher VCP emissions than the NEI for approximately half of all counties, with 5 % of all counties having greater than 55 % higher emissions. Categorically, application of the VCPy framework yields higher emissions for personal care products (150 %) and paints and coatings (25 %) when compared to the NEI, whereas pesticides (−54 %) and printing inks (−13 %) feature lower emissions. An observational evaluation indicates emissions of key species from VCPs are reproduced with high fidelity using the VCPy framework (normalized mean bias of −13 % with r = 0.95). Sector-wide, the effective secondary organic aerosol yield and maximum incremental reactivity of VCPs are 5.3 % by mass and 1.58 g O3 g−1, respectively, indicating VCPs are an important, and likely to date underrepresented, source of secondary pollution in urban environments.

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“…Biogenic emissions of VOCs are most commonly estimated using models such as the Model of Emissions of Gases and Aerosols from Nature (MEGAN) [16], whilst AVOC emissions are most commonly estimated using regional or global emissions inventories such as the Emission Database for Global Atmospheric Research (EDGAR) [26]. Despite the refinement of these techniques over recent years, large uncertainties remain in estimated emissions of BVOCs and AVOCs in many parts of the world [27][28][29][30][31][32], with Australia a particularly poorly characterised region [33,34].…”

Section: Introductionmentioning

confidence: 99%

Seasonal Variation of Biogenic and Anthropogenic VOCs in a Semi-Urban Area Near Sydney, Australia

et al. 2020

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Volatile organic compounds (VOCs) play a key role in the formation of ozone and secondary organic aerosol, the two most important air pollutants in Sydney, Australia. Despite their importance, there are few available VOC measurements in the area. In this paper, we discuss continuous GC-MS measurements of 10 selected VOCs between February (summer in the southern hemisphere) and June (winter in the southern hemisphere) of 2019 in a semi-urban area between natural eucalypt forest and the Sydney metropolitan fringe. Combined, isoprene, methacrolein, methyl-vinyl-ketone, α-pinene, p-cymene, eucalyptol, benzene, toluene xylene and tri-methylbenzene provide a reasonable representation of variability in the total biogenic VOC (BVOC) and anthropogenic VOC (AVOC) loading in the area. Seasonal changes in environmental conditions were reflected in observed BVOC concentrations, with a summer peak of 8 ppb, dropping to approximately 0.1 ppb in winter. Isoprene, and its immediate oxidation products methacrolein (MACR) and methyl-vinyl-ketone (MVK), dominated BVOC concentrations during summer and early autumn, while monoterpenes comprised the larger fraction during winter. Temperature and solar radiation drive most of the seasonal variation observed in BVOCs. Observed levels of isoprene, MACR and MVK in the atmosphere are closely related with variations in temperature and photosynthetically active radiation (PAR), but chemistry and meteorology may play a more important role for the monoterpenes. Using a nonlinear model, temperature explains 51% and PAR 38% of the isoprene, MACR and MVK variation. Eucalyptol dominated the observed monoterpene fraction (contributing ~75%), with p-cymene (20%) and α-pinene (5%) also present. AVOCs maintain an average concentration of ~0.4 ppb, with a slight decrease during autumn–winter. The low AVOC concentrations observed indicate a relatively small anthropogenic influence, generally occurring when (rare) northerly winds transport Sydney emissions to the measurement site. The site is influenced by domestic, commercial and vehicle AVOC emissions. Our observed AVOC concentrations can be explained by the seasonal changes in meteorology and the emissions in the area as listed in the NSW emissions inventory and thereby act as an independent validation of this inventory. We conclude that the variations in atmospheric composition observed during the seasons are an important variable to consider when formulating air pollution control policies over Sydney given the influence of biogenic sources during summer, autumn and winter.

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An uncertainty for clean air: Air quality modeling implications of underestimating VOC emissions in urban inventories

Cited by 24 publications

References 115 publications

Changes in speciated PM2.5 concentrations in Fresno, California, due to NOx reductions and variations in diurnal emission profiles by day of week

Changes in speciated PM2.5 concentrations in Fresno, California, due to NOx reductions and variations in diurnal emission profiles by day of week

Reactive organic carbon emissions from volatile chemical products

Seasonal Variation of Biogenic and Anthropogenic VOCs in a Semi-Urban Area Near Sydney, Australia

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