T
Tim C. Keener
Researcher at University of Cincinnati
Publications - 127
Citations - 2605
Tim C. Keener is an academic researcher from University of Cincinnati. The author has contributed to research in topics: Flue gas & Sorbent. The author has an hindex of 29, co-authored 127 publications receiving 2339 citations. Previous affiliations of Tim C. Keener include United States Environmental Protection Agency & United States Department of Health and Human Services.
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Potential flue gas impurities in carbon dioxide streams separated from coal-fired power plants.
TL;DR: The formation rates of heat-stable salts in MEA solution are critical to estimating the levels and compositions of flue gas impurities in sequestered CO2 streams and warrant necessary considerations in overall sequestration planning, engineering, and management.
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The organic composition of diesel particulate matter, diesel fuel and engine oil of a non-road diesel generator
TL;DR: The composition of DPM suggests that they may be originated from unburned diesel fuel, engine oil evaporation and combustion generated products, with the shift toward higher molecular weight ones.
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Development of cost-effective noncarbon sorbents for Hg(0) removal from coal-fired power plants.
TL;DR: Several functionalized silica materials reported in previous studies to effectively control heavy metals in the aqueous phase showed insignificant adsorption capacities for Hg(0) control in the gas phase, suggesting that mercury removal mechanisms in both phases are different.
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Ammonia-treated porous carbon derived from ZIF-8 for enhanced CO2 adsorption
TL;DR: In this article, a porous carbon (ZC) was prepared at 900°C using zeolitic imidazolate framework-8 (ZIF-8) as a solid template for CO 2 adsorption.
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Bench-scale studies of in-duct mercury capture using cupric chloride-impregnated carbons.
TL;DR: The bench-scale entrained-flow system was able to demonstrate the important Hg adsorption and oxidation characteristics of the tested sorbents and sorbent deposition on walls was significantly reduced so that additional mercury capture by the deposited sorbent was minimized.