Publications by authors named "P Ziemann"

Atmospheric simulation chambers continue to be indispensable tools for research in the atmospheric sciences. Insights from chamber studies are integrated into atmospheric chemical transport models, which are used for science-informed policy decisions. However, a centralized data management and access infrastructure for their scientific products had not been available in the United States and many parts of the world.

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Indoor gas-phase radical sources are poorly understood but expected to be much different from outdoors. Several potential radical sources were measured in a windowless, light-emitting diode (LED)-lit room in a college athletic facility over a 2 week period. Alternating measurements between the room air and the supply air of the heating, ventilation, and air-conditioning system allowed an assessment of sources.

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The oxidation of volatile organic compounds (VOCs), which are emitted to the atmosphere from natural and anthropogenic sources, leads to the formation of ozone and secondary organic aerosol (SOA) particles that impact air quality and climate. In the study reported here, we investigated the products of the reactions of five biogenic monoterpenes with OH radicals (an important daytime oxidant) under conditions that mimic the chemistry that occurs in polluted air, and developed mechanisms to explain their formation. Experiments were conducted in an environmental chamber, and information on the identity of gas-phase molecular products was obtained using online mass spectrometry, while liquid chromatography and two methods of functional group analysis were used to characterize the SOA composition.

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Dark chamber experiments were conducted to study the SOA formed from the oxidation of α-pinene and Δ-carene under different peroxy radical (RO) fate regimes: RO + NO, RO + RO, and RO + HO. SOA mass yields from α-pinene oxidation were <1 to ∼25% and strongly dependent on available OA mass up to ∼100 μg m. The strong yield dependence of α-pinene oxidation is driven by absorptive partitioning to OA and not by available surface area for condensation.

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Atmospheric organic aerosol particles impact climate as well as human and environmental health. Secondary organic aerosol (SOA), which is formed by the gas-to-particle partitioning of products of the oxidation of volatile organic compounds (VOCs) emitted from biogenic or anthropogenic sources, contributes a large fraction of this material. In the particle phase, these products can undergo accretion reactions to form oligomers that impact the formation, composition, and chemical-physical properties of aerosols.

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