Publications by authors named "Nijing Wang"

New particle formation (NPF) in the tropical upper troposphere is a globally important source of atmospheric aerosols. It is known to occur over the Amazon basin, but the nucleation mechanism and chemical precursors have yet to be identified. Here we present comprehensive in situ aircraft measurements showing that extremely low-volatile oxidation products of isoprene, particularly certain organonitrates, drive NPF in the Amazonian upper troposphere.

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Personal care products (PCPs) contain diverse volatile organic compounds (VOCs) and routine use of PCPs indoors has important implications for indoor air quality and human chemical exposures. This chamber study deployed aerosol instrumentation and two online mass spectrometers to quantify VOC emissions from the indoor use of five fragranced PCPs and examined the formation of gas-phase oxidation products and particles upon ozone-initiated oxidation of reactive VOCs. The tested PCPs include a perfume, a roll-on deodorant, a body spray, a hair spray, and a hand lotion.

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Humans are known to be a continuous and potent indoor source of volatile organic compounds (VOCs). However, little is known about how personal hygiene, in terms of showering frequency, can influence these emissions and their impact on indoor air chemistry involving ozone. In this study, we characterized the VOC composition of the air in a controlled climate chamber (22.

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A major component of human skin oil is squalene, a highly unsaturated hydrocarbon that protects the skin from atmospheric oxidants. Skin oil, and thus squalene, is continuously replenished on the skin surface. Squalene is also quickly consumed through reactions with ozone and other oxidants.

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Ozone reaction with human surfaces is an important source of ultrafine particles indoors. However, 1-20 nm particles generated from ozone-human chemistry, which mark the first step of particle formation and growth, remain understudied. Ventilation and indoor air movement could have important implications for these processes.

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Article Synopsis
  • Hydroxyl (OH) radicals, which can oxidize various pollutant gases, were found at high levels when individuals were exposed to ozone in a controlled environment.
  • The study utilized two methods to measure OH concentrations, which aligned with results from a detailed chemical model.
  • A compound called 6-methyl-5-hepten-2-one (6-MHO) plays a crucial role in generating OH when ozone reacts with skin oil, affecting indoor air chemistry and potentially human health.
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Article Synopsis
  • Carbon dioxide (CO) and methane (CH) are significant greenhouse gases affecting Earth's climate, but human metabolic emissions of these gases have not been extensively studied.
  • A research study measured CO and CH emissions from 20 volunteers under controlled conditions, finding individual differences greatly impacted CH emissions, while CO emissions increased with temperature.
  • The study revealed that one-third of participants were significant CH producers and suggests that as global populations grow and human-made emissions decrease, CH emissions from people may become more relevant in the overall carbon budget.
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Human-emitted volatile organic compounds (VOCs) are mainly from breath and the skin. In this study, we continuously measured VOCs in a stainless-steel environmentally controlled climate chamber (22.5 m, air change rate at 3.

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Nanocluster aerosols (NCAs, particles <3 nm) are important players in driving climate feedbacks and processes that impact human health. This study reports, for the first time, NCA formation when gas-phase ozone reacts with human surfaces. In an occupied climate-controlled chamber, we detected NCA only when ozone was present.

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People influence indoor air chemistry through their chemical emissions via breath and skin. Previous studies showed that direct measurement of total OH reactivity of human emissions matched that calculated from parallel measurements of volatile organic compounds (VOCs) from breath, skin, and the whole body. In this study, we determined, with direct measurements from two independent groups of four adult volunteers, the effect of indoor temperature and humidity, clothing coverage (amount of exposed skin), and indoor ozone concentration on the total OH reactivity of gaseous human emissions.

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Humans are a potent, mobile source of various volatile organic compounds (VOCs) in indoor environments. Such direct anthropogenic emissions are gaining importance, as those from furnishings and building materials have become better regulated and energy efficient homes may reduce ventilation. While previous studies have characterized human emissions in indoor environments, the question remains whether VOCs remain unidentified by current measuring techniques.

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Many bird species have the ability to navigate home after being brought to a remote, even unfamiliar location. Environmental odours have been demonstrated to be critical to homeward navigation in over 40 years of experiments, yet the chemical identity of the odours has remained unknown. In this study, we investigate potential chemical navigational cues by measuring volatile organic compounds (VOCs): at the birds' home-loft; in selected regional forest environments; and from an aircraft at 180 m.

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With the gradual reduction of emissions from building products, emissions from human occupants become more dominant indoors. The impact of human emissions on indoor air quality is inadequately understood. The aim of the Indoor Chemical Human Emissions and Reactivity (ICHEAR) project was to examine the impact on indoor air chemistry of whole-body, exhaled, and dermally emitted human bioeffluents under different conditions comprising human factors (t-shirts/shorts vs long-sleeve shirts/pants; age: teenagers, young adults, and seniors) and a variety of environmental factors (moderate vs high air temperature; low vs high relative humidity; presence vs absence of ozone).

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Previous work examining the condensed-phase products of squalene particle ozonolysis found that an increase in water vapor concentration led to lower concentrations of secondary ozonides, increased concentrations of carbonyls, and smaller particle diameter, suggesting that water changes the fate of the Criegee intermediate. To determine if this volume loss corresponds to an increase in gas-phase products, we measured gas-phase volatile organic compound (VOC) concentrations via proton-transfer-reaction time-of-flight mass spectrometry. Studies were conducted in a flow-tube reactor at atmospherically relevant ozone (O) exposure levels (5-30 ppb h) with pure squalene particles.

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We present a sensitive and quick way to determine benzene, toluene and dimethylbenzene (BTEX) in air, applying a cataluminescence (CTL) sensor based on a nano-sized composite material, γ-Al2O3/PtO2. The factors that affect the sensor's performance were studied, including the sensing material, temperature, rate of air carrier and wavelength. It was shown that when Pt accounted for 0.

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