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The emergence of low-cost air quality sensors as viable tools for the monitoring of air quality at population and individual levels necessitates the evaluation of these instruments. The Flow air quality tracker, a product of Plume Labs, is one such sensor. To evaluate these sensors, we assessed 34 of them in a controlled laboratory setting by exposing them to PM 10 and PM 2.5 and compared the response with Plantower A003 measurements. The overall coefficient of determination (R 2 ) of measured PM 2.5 was 0.76 and of PM 10 it was 0.73, but the Flows' accuracy improved after each introduction of incense. Overall, these findings suggest that the Flow can be a useful air quality monitoring tool in air pollution areas with higher concentrations, when incorporated into other monitoring frameworks and when used in aggregate. The broader environmental implications of this work are that it is possible for individuals and groups to monitor their individual exposure to particulate matter pollution.

Tens of millions of individuals go to gasoline stations on a daily basis in the United States. One of the constituents of gasoline is benzene, a Group 1 carcinogen that has been strongly linked to both occupational and non-occupational leukemias. While benzene content in gasoline is federally regulated, there is approximately a thirty-year data gap in United States research on benzene exposures from pumping gasoline. Using a novel self-sampling protocol with whole air canisters, we conducted a gasoline pumping exposure assessment for benzene, toluene, ethylbenzene, and xylene (BTEX) on Baltimore, MD consumers. Geometric mean exposures (geometric standard deviations) were 3.2 (2.7) ppb,9.5 (3.5) ppb, 2.0 (2.8) ppb, and 7.3 (3.0) ppb, respectively, on 32 samples. Using the benzene exposures, we conducted consumer and occupational probabilistic risk assessments and contextualized the risk with ambient benzene exposure risk. We found that the consumer scenarios did not approach the 1:1,000,000 excess risk management threshold and that the occupational scenario did not exceed the 1:10,000 excess risk management threshold. Further, in all Monte Carlo trials, the ambient risk from benzene exposure exceeded that of pumping risk for consumers, but that in approximately 30% of occupational trials, the pumping risk exceeded the ambient risk.

Due to the rapid development of low-cost air-quality sensors, a rigorous scientific evaluation has not been conducted for many available sensors. We evaluated three Plantower PMS A003 sensors when exposed to eight particulate matter (PM) sources (i.e., incense, oleic acid, NaCl, talcum powder, cooking emissions, and monodispersed polystyrene latex spheres under controlled laboratory conditions and also residential air and ambient outdoor air in Baltimore, MD). The PM 2.5 sensors exhibited a high degree of precision and R 2 values greater than 0.86 for all sources, but the accuracy ranged from 13 to >90% compared with reference instruments. The sensors were most accurate for PM with diameters below 1 μm, and they poorly measured PM in the 2.5-5 μm range. The accuracy of the sensors was dependent on relative humidity (RH), with decreases in accuracy at RH > 50%. The sensors were able to produce meaningful data at low and high temperatures and when in motion, as it would be if utilized for outdoor or personal monitoring applications. It was most accurate in environments with polydispersed particle sources and may not be useful in specialized environments or experiments with narrow distributions of PM or aerosols with a large proportion of coarse PM.

In this study, we characterized personal exposure to fine particulate matter (PM 2.5 ), black carbon (BC), and nicotine in pregnant women in Hidalgo County, where the hospitalization rates of childhood asthma are the highest in the state of Texas. The measurements were conducted over three non-consecutive sampling days for 17 participants in their third trimester. Measurements were partitioned into four microenvironments, i.e., Residential, Vehicular, Commercial, and Other, on the basis of GPS coordinates and temperature and humidity measurements. The daily average PM 2.5 mass concentration was 24.2 (standard deviation=22.0) μg/m 3 , with the highest daily mass concentration reaching 126.0μg/m 3 . The daily average BC concentration was 1.44 (SD=0.82) μg/m 3 , ranging from 0.5 to 5.4μg/m 3 . Hair nicotine concentrations were all near the detection level (i.e., 49.2pg/mg), indicating that the participants were not routinely exposed to tobacco smoke. The Residential microenvironment contributed dominantly to the mass concentration since the participants chiefly remained at home and cooking activities contributed significantly to the total PM 2.5 . When compared to an ambient monitoring station, the person-specific PM 2.5 was frequently more than double the ambient measurement (10.4μg/m 3 overall), revealing that even in regions where ambient concentrations are below national standards, individuals may be still be exposed to elevated PM 2.5 mass concentrations., (Copyright © 2018 Elsevier B.V. All rights reserved.)

Sulfate aerosols exert profound impacts on human and ecosystem health, weather, and climate, but their formation mechanism remains uncertain. Atmospheric models consistently underpredict sulfate levels under diverse environmental conditions. From atmospheric measurements in two Chinese megacities and complementary laboratory experiments, we show that the aqueous oxidation of SO 2 by NO 2 is key to efficient sulfate formation but is only feasible under two atmospheric conditions: on fine aerosols with high relative humidity and NH 3 neutralization or under cloud conditions. Under polluted environments, this SO 2 oxidation process leads to large sulfate production rates and promotes formation of nitrate and organic matter on aqueous particles, exacerbating severe haze development. Effective haze mitigation is achievable by intervening in the sulfate formation process with enforced NH 3 and NO 2 control measures. In addition to explaining the polluted episodes currently occurring in China and during the 1952 London Fog, this sulfate production mechanism is widespread, and our results suggest a way to tackle this growing problem in China and much of the developing world., Competing Interests: The authors declare no conflict of interest.

Black carbon (BC) exerts profound impacts on air quality and climate because of its high absorption cross-section over a broad range of electromagnetic spectra, but the current results on absorption enhancement of BC particles during atmospheric aging remain conflicting. Here, we quantified the aging and variation in the optical properties of BC particles under ambient conditions in Beijing, China, and Houston, United States, using a novel environmental chamber approach. BC aging exhibits two distinct stages, i.e., initial transformation from a fractal to spherical morphology with little absorption variation and subsequent growth of fully compact particles with a large absorption enhancement. The timescales to achieve complete morphology modification and an absorption amplification factor of 2.4 for BC particles are estimated to be 2.3 h and 4.6 h, respectively, in Beijing, compared with 9 h and 18 h, respectively, in Houston. Our findings indicate that BC under polluted urban environments could play an essential role in pollution development and contribute importantly to large positive radiative forcing. The variation in direct radiative forcing is dependent on the rate and timescale of BC aging, with a clear distinction between urban cities in developed and developing countries, i.e., a higher climatic impact in more polluted environments. We suggest that mediation in BC emissions achieves a cobenefit in simultaneously controlling air pollution and protecting climate, especially for developing countries.