L
L. King
Researcher at Georgia Institute of Technology
Publications - 14
Citations - 1294
L. King is an academic researcher from Georgia Institute of Technology. The author has contributed to research in topics: Aerosol & Particle. The author has an hindex of 11, co-authored 13 publications receiving 964 citations.
Papers
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Journal ArticleDOI
Contribution of Water-Soluble and Insoluble Components and Their Hydrophobic/Hydrophilic Subfractions to the Reactive Oxygen Species-Generating Potential of Fine Ambient Aerosols
Vishal Verma,Roberto Rico-Martínez,Neel Kotra,L. King,Jiumeng Liu,Terry W. Snell,Rodney J. Weber +6 more
TL;DR: It is suggested that the hydrophobic components of both water-soluble and insoluble organic aerosols substantially contribute to the oxidative properties of ambient PM.
Journal ArticleDOI
Size-resolved measurements of brown carbon in water and methanol extracts and estimates of their contribution to ambient fine-particle light absorption
Jiumeng Liu,Michael H. Bergin,Hongyu Guo,L. King,Neel Kotra,Eric S. Edgerton,Rodney J. Weber +6 more
TL;DR: In this paper, size-resolved direct measurements of brown carbon were made at both urban (Atlanta), and rural (Yorkville) sites in Georgia, and brown carbon absorption was estimated based on Mie calculations using direct size-resolution measurements of chromophores in solvents.
Journal ArticleDOI
Reactive oxygen species associated with water-soluble PM 2.5 in the southeastern United States: spatiotemporal trends and source apportionment
Vishal Verma,Ting Fang,Hongyu Guo,L. King,Josephine T. Bates,Richard E. Peltier,Eric S. Edgerton,Armistead G. Russell,Rodney J. Weber +8 more
TL;DR: In this paper, the potential of the water-soluble fraction of atmospheric fine aerosols in the southeastern United States to generate reactive oxygen species (ROS) and identify major ROS-associated emission sources was quantified by the dithiothreitol (DTT) assay and involved analysis of fine particulate matter (PM) extracted from high-volume quartz filters (23 h integrated samples) collected at various sites in different environmental settings in the southeast, including three urban-Atlanta sites, in addition to a rural site.
Journal ArticleDOI
Airborne measurements of western U.S. wildfire emissions: Comparison with prescribed burning and air quality implications
Xiaoxi Liu,Xiaoxi Liu,Xiaoxi Liu,L. Gregory Huey,Robert J. Yokelson,Vanessa Selimovic,Isobel J. Simpson,Markus Müller,Markus Müller,Jose L. Jimenez,Jose L. Jimenez,Pedro Campuzano-Jost,Pedro Campuzano-Jost,Andreas J. Beyersdorf,Andreas J. Beyersdorf,Donald R. Blake,Zachary Butterfield,Zachary Butterfield,Yonghoon Choi,John D. Crounse,Douglas A. Day,Douglas A. Day,Glenn S. Diskin,Manvendra K. Dubey,Edward C. Fortner,Thomas F. Hanisco,Weiwei Hu,Weiwei Hu,L. King,Lawrence I. Kleinman,Simone Meinardi,Tomas Mikoviny,Timothy B. Onasch,Brett B. Palm,Brett B. Palm,Jeff Peischl,Jeff Peischl,Ilana B. Pollack,Ilana B. Pollack,Ilana B. Pollack,Thomas B. Ryerson,Glen W. Sachse,Arthur J. Sedlacek,John E. Shilling,Stephen R. Springston,Jason M. St. Clair,Jason M. St. Clair,Jason M. St. Clair,David J. Tanner,Alex P. Teng,Paul O. Wennberg,Armin Wisthaler,Armin Wisthaler,Glenn M. Wolfe,Glenn M. Wolfe +54 more
TL;DR: In this paper, an extensive set of emission factors (EFs) for over 80 gases and 5 components of submicron particulate matter (PM_1) from three wildfires in the western U.S. were measured from aircraft during the Studies of Emissions and Atmospheric Composition, Clouds and Climate Coupling by Regional Surveys (SEAC^4RS) and the Biomass Burning Observation Project (BBOP).
Journal ArticleDOI
A semi-automated system for quantifying the oxidative potential of ambient particles in aqueous extracts using the dithiothreitol (DTT) assay: Results from the Southeastern Center for Air Pollution and Epidemiology (SCAPE)
TL;DR: In this article, a semi-automated system for quantifying the oxidative potential of aerosol liquid extracts using the DTT assay was developed, capable of unattended analysis at one sample per hour, and reasonably low limit of detection (0.31 nmol min−1).