Poor air quality is globally the largest environmental health risk. Epidemiological studies have uncovered clear relationships of gaseous pollutants and particulate matter (PM) with adverse health outcomes, including mortality by cardiovascular and respiratory diseases. Studies of health impacts by aerosols are highly multidisciplinary with a broad range of scales in space and time. We assess recent advances and future challenges regarding aerosol effects on health from molecular to global scales through epidemiological studies, field measurements, health-related properties of PM, and multiphase interactions of oxidants and PM upon respiratory deposition. Global modeling combined with epidemiological exposure-response functions indicates that ambient air pollution causes more than four million premature deaths per year. Epidemiological studies usually refer to PM mass concentrations, but some health effects may relate to specific constituents such as bioaerosols, polycyclic aromatic compounds, and transition metals. Various analytical techniques and cellular and molecular assays are applied to assess the redox activity of PM and the formation of reactive oxygen species. Multiphase chemical interactions of lung antioxidants with atmospheric pollutants are crucial to the mechanistic and molecular understanding of oxidative stress upon respiratory deposition. The role of distinct PM components in health impacts and mortality needs to be clarified by integrated research on various spatiotemporal scales for better evaluation and mitigation of aerosol effects on public health in the Anthropocene.
Abstract. Traditional yield curve analysis shows that semi-volatile organic compounds are a major component of secondary organic aerosols (SOAs). We investigated the volatility distribution of SOAs from α-pinene ozonolysis using positive electrospray ionization mass analysis and dilution- and heat-induced evaporation measurements. Laboratory chamber experiments were conducted on α-pinene ozonolysis, in the presence and absence of OH scavengers. Among these, we identified not only semi-volatile products, but also less volatile highly oxygenated molecules (HOMs) and dimers. Ozonolysis products were further exposed to OH radicals to check the effects of photochemical aging. HOMs were also formed during OH-initiated photochemical aging. Most HOMs that formed from ozonolysis and photochemical aging had 10 or fewer carbons. SOA particle evaporation after instantaneous dilution was measured at < 1 and ∼ 40 % relative humidity. The volume fraction remaining of SOAs decreased with time and the equilibration timescale was determined to be 24–46 min for SOA evaporation. The experimental results of the equilibration timescale can be explained when the mass accommodation coefficient is assumed to be 0.1, suggesting that the existence of low-volatility materials in SOAs, kinetic inhibition, or some combined effect may affect the equilibration timescale measured in this study.
Abstract. Studies of the volatility distribution of secondary
organic aerosol (SOA) from aromatic compounds are limited compared with SOA
from biogenic monoterpenes. In this study, the volatility distribution was
investigated by composition, heating, and dilution measurements for SOA
formed from the photooxidation of 1,3,5-trimethylbenzene in the presence of
NOx. Composition studies revealed that highly oxygenated monomers
(C9H14Ox, x = 4–7) and dimers (C18H26Ox, x = 8–12) are the major products in SOA particles. Highly oxygenated
molecules (HOMs) with five or more oxygens were formed during photochemical
aging, whereas dimers degraded during photochemical aging. HOMs with five or
more oxygens may be produced from the photooxidation of phenol-type gaseous
products, whereas dimers in the particle phase may be photolyzed to smaller
molecules during photochemical aging. The results of composition, heating,
and dilution measurements showed that fresh SOA that formed from
1,3,5-trimethylbenzene (TMB) photooxidation includes low-volatility compounds with
<1 µg m−3 saturation concentrations, which are
attributed to dimers. Similar results were reported for α-pinene SOA
in previous studies. Low-volatility compounds with <1 µg m−3 saturation concentrations are not included in the
volatility distributions employed in the standard volatility basis-set (VBS) approach. Improvements
in the organic aerosol model will be necessary for the study of anthropogenic
SOA as well as biogenic SOA.
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