Hyeon Ung Shin
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Hyeon Ung Shin has a total of 4 co-authors. Here are the top co-authors by number of shared publications:
- Dinesh Lolla
Biosciences and Water Filtration Division, Parker-Hannifin Corporation, Oxnard, CA 93030, USA
2 shared publications - George G. Chase
Department of Chemical and Biomolecular Engineering, The University of Akron 1 , 185 E. Mill St., Akron, Ohio 44325, USA
2 shared publications - Ahmed Abutaleb
Department of Chemical Engineering, College of Engineering and Computer Sciences, Jazan University, Jazan 45142, Saudi Arabia
1 shared publication - Jonathan W. Rajala
Department of Chemical and Biomolecular Engineering, The University of Akron, Akron, OH 44325, USA
1 shared publication
Latest Publications
- Open Access
Effect of Calcination Temperature on NO–CO Decomposition by Pd Catalyst Nanoparticles Supported on Alumina Nanofibers
In this work, palladium (Pd) nanoparticles were blended into a solution of a sacrificial polymer and an aluminum sol gel precursor to form alumina fibers containing the palladium particles. The polymer solution was electrospun into template submicron fibers. These fibers were calcined at temperatures between 650 °C and 1150 °C to remove the polymer and oxidize the aluminum. The internal crystalline morphologies of the calcined fibers transformed with change in the calcination temperature. The calcined fibers were formed into fibrous mats and further tested for their catalytic performances. The Pd particles had a size ranging from 5–20 nm and appeared randomly distributed within and near the surfaces of the alumina fibers. The final metal loading of all Pd/Al2O3 samples ranged from 4.7 wt % to 5.1 wt %. As calcination temperature increased the alumina crystal structure changed from amorphous at 650 °C to alpha crystal structure at 1150 °C. With the increase of calcination temperature, the average fiber diameters and specific surface areas decreased. The catalyst supported fiber media had good conversion of NO and CO gases. Higher calcination temperatures led to higher reaction temperatures from 250 to about 450 °C for total conversion, indicating the effective reactivity of the fiber-supported catalysts decreased with increase in calcination temperature. The fibers formed at the 650 °C calcination temperature had the highest reaction activity.
Open AccessEffect of Calcination Temperature on NO–CO Decomposition by Pd Catalyst Nanoparticles Supported on Alumina Nanofibers
In this work, palladium (Pd) nanoparticles were blended into a solution of a sacrificial polymer and an aluminum sol gel precursor to form alumina fibers containing the palladium particles. The polymer solution was electrospun into template submicron fibers. These fibers were calcined at temperatures between 650 °C and 1150 °C to remove the polymer and oxidize the aluminum. The internal crystalline morphologies of the calcined fibers transformed with change in the calcination temperature. The calcined fibers were formed into fibrous mats and further tested for their catalytic performances. The Pd particles had a size ranging from 5–20 nm and appeared randomly distributed within and near the surfaces of the alumina fibers. The final metal loading of all Pd/Al2O3 samples ranged from 4.7 wt % to 5.1 wt %. As calcination temperature increased the alumina crystal structure changed from amorphous at 650 °C to alpha crystal structure at 1150 °C. With the increase of calcination temperature, the average fiber diameters and specific surface areas decreased. The catalyst supported fiber media had good conversion of NO and CO gases. Higher calcination temperatures led to higher reaction temperatures from 250 to about 450 °C for total conversion, indicating the effective reactivity of the fiber-supported catalysts decreased with increase in calcination temperature. The fibers formed at the 650 °C calcination temperature had the highest reaction activity.
- Open Access
Core–Shell Electrospun Hollow Aluminum Oxide Ceramic Fibers
In this work, core–shell electrospinning was employed as a simple method for the fabrication of composite coaxial polymer fibers that became hollow ceramic tubes when calcined at high temperature. The shell polymer solution consisted of polyvinyl pyrollidone (PVP) in ethanol mixed with an aluminum acetate solution to act as a ceramic precursor. The core polymer was recycled polystyrene to act as a sacrificial polymer that burned off during calcination. The resulting fibers were analyzed with X-ray diffraction (XRD) and energy dispersive spectroscopy (EDS) to confirm the presence of gamma-phase aluminum oxide when heated at temperatures above 700 °C. The fiber diameter decreased from 987 ± 19 nm to 382 ± 152 nm after the calcination process due to the polymer material being burned off. The wall thickness of these fibers is estimated to be 100 nm.
Open AccessCore–Shell Electrospun Hollow Aluminum Oxide Ceramic Fibers
In this work, core–shell electrospinning was employed as a simple method for the fabrication of composite coaxial polymer fibers that became hollow ceramic tubes when calcined at high temperature. The shell polymer solution consisted of polyvinyl pyrollidone (PVP) in ethanol mixed with an aluminum acetate solution to act as a ceramic precursor. The core polymer was recycled polystyrene to act as a sacrificial polymer that burned off during calcination. The resulting fibers were analyzed with X-ray diffraction (XRD) and energy dispersive spectroscopy (EDS) to confirm the presence of gamma-phase aluminum oxide when heated at temperatures above 700 °C. The fiber diameter decreased from 987 ± 19 nm to 382 ± 152 nm after the calcination process due to the polymer material being burned off. The wall thickness of these fibers is estimated to be 100 nm.