Yong-Kul Lee

ORCID: 0000-0001-6800-556X
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About
Contact & Profiles
Research Areas
  • Catalysis and Hydrodesulfurization Studies
  • Catalytic Processes in Materials Science
  • Electrocatalysts for Energy Conversion
  • Petroleum Processing and Analysis
  • Nanomaterials for catalytic reactions
  • Catalysis for Biomass Conversion
  • Catalysts for Methane Reforming
  • Catalysis and Oxidation Reactions
  • Enhanced Oil Recovery Techniques
  • Advanced battery technologies research
  • Zeolite Catalysis and Synthesis
  • Electrochemical Analysis and Applications
  • Hydrocarbon exploration and reservoir analysis
  • Fuel Cells and Related Materials
  • Polymer crystallization and properties
  • Corrosion Behavior and Inhibition
  • Subcritical and Supercritical Water Processes
  • Thermochemical Biomass Conversion Processes
  • Advancements in Battery Materials
  • Metal Extraction and Bioleaching
  • Environmental remediation with nanomaterials
  • biodegradable polymer synthesis and properties
  • Carbon dioxide utilization in catalysis
  • Machine Learning in Materials Science
  • Biodiesel Production and Applications

Dankook University
2015-2024

Virginia Tech
2003-2024

Yong In University
2017-2021

Government of the Republic of Korea
2021

Commissariat à l'Énergie Atomique et aux Énergies Alternatives
2017

Seoul National University
1998-2008

Korea Institute of Science and Technology
2008

National Institute of Advanced Industrial Science and Technology
2007

National Pingtung University of Science and Technology
2004

Pennsylvania State University
1999

Silica-supported manganese oxide catalysts with loadings of 3, 10, 15, and 20 wt % (as MnO2) were characterized use X-ray absorption spectroscopy diffraction (XRD). The edge positions in the spectra indicated that oxidation state for decreased increasing metal loading from a value close to Mn2O3 (+3) Mn3O4 (+2(2)/3). XRD was consistent these results as diffractograms supported higher matched those reference. reactivity silica-supported acetone ozone an oxidant studied over temperature range...

10.1021/jp054288w article EN The Journal of Physical Chemistry B 2006-02-08

Effects of nitrogen compounds, aromatics, and aprotic solvents on the oxidative desulfurization (ODS) refractory sulfur compounds light cycle oil over Ti-SBA-15 catalyst were studied in a batch or continuous fixed-bed reactor with tert-butyl hydroperoxide (TBHP) as oxidant. The fresh spent catalysts characterized by BET, TGA, ICP-AES, X-ray absorption spectroscopy. found to inhibit ODS order: indole > quinoline carbazole. addition aromatics solvent feed gradually recovered activity for LCO....

10.1016/j.apcatb.2013.08.017 article EN cc-by-nc-nd Applied Catalysis B Environment and Energy 2013-08-29

Supported manganese oxide catalysts were prepared by the impregnation of alumina foam blocks washcoated with and silica. The content based on weight washcoats was 10 wt % calculated as MnO2. Fourier transform profiles Mn K-edge EXAFS spectra for these samples gave three distinctive peaks at 0.15, 0.25, 0.32 nm close to Mn3O4 β-MnO2. number surface active sites determined through oxygen chemisorption measurements a reduction temperature (Tred = 443 K) obtained from temperature-programmed...

10.1021/jp052930g article EN The Journal of Physical Chemistry B 2005-08-24

The kinetics for the initial stage of hydrodesulfurization (HDS) 4,6-dimethyldibenzothiophene (4,6-DMDBT) and dibenzothiophene (DBT) were comparatively examined over NiMo CoMo sulfide catalysts newly developed nickel phosphide catalysts. HDS can proceed through an indirect hydrogenation (HYD) pathway a direct desulfurization (DDS, or hydrogenolysis) pathway. rate constants HYD DDS pathways (k1 k2, respectively) estimated using method that involved extrapolation to zero conversion selectivity...

10.1021/ef049804g article EN Energy & Fuels 2005-02-04

10.1016/j.apcatb.2019.01.087 article EN Applied Catalysis B Environment and Energy 2019-01-31
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