Korea University · Engineering
Professor Hyun Wook Jung's research lab specializes in the design, synthesis, and characterization of advanced polymeric materials, with a focus on hydrogels, electrospun nanofibers, and functional coatings. The lab investigates crosslinking dynamics, gelation mechanisms, and stimuli-responsive behaviors in poly(ethylene glycol)-based hydrogels, as well as the development of novel crosslinkers for low-temperature curing applications. Key research directions include the control of polymer network structures through UV and thermal polymerization, the engineering of nanofibrous architectures using electrospinning, and the optimization of material properties for biomedical and industrial applications. The lab combines advanced analytical techniques such as rheology, FT-IR spectroscopy, and thermal analysis to understand structure-property relationships in soft materials.
Figures are computed from collected data and may differ slightly.
Abstract Electrospinning experiments for solutions of two polymers with different crystallization rates, polylatic acid (PLA), and nylon 6 solutions have been carried out. Hexafluoroisopropanol (HFIP) was used as a common solvent to dissolve both PLA and nylon 6. Using the fact that nylon 6 has the faster crystallization rate than PLA, the effect of thermal annealing conditions on the crystal structures of two electrospun fibers has mainly been studied via thermal and mechanical analysis. First,
ABSTRACT The gelation and crosslinking features of poly(ethylene glycol) (PEG) hydrogels were scrutinized through the UV polymerization processes of poly(ethylene glycol) methacrylate (PEGMA) and poly(ethylene glycol) dimethacrylate (PEGDMA) mixtures. The real‐time evolutions of the elastic moduli of the prepolymerized mixtures with different crosslinking ratios of PEGMA and PEGDMA and the photoinitiator concentrations were measured during photopolymerization. The rheological properties were com
This study investigates the crosslinking dynamics and swelling properties of pH-responsive poly(ethylene glycol) (PEG)/poly(acrylic acid) (PAA) interpenetrating polymer network (IPN) hydrogels. These hydrogels feature denser crosslinked networks compared to PEG single network (SN) hydrogels. Fabrication involved a two-step UV curing process: First, forming PEG-SN hydrogels using poly(ethylene glycol) diacrylate (PEGDA) through UV-induced free radical polymerization and crosslinking reactions, th
The crosslinking behaviors and gelation features of poly(ethylene glycol) (PEG) hydrogels were scrutinized during the UV and thermal polymerizations of mixtures of poly(ethylene glycol) methacrylate (PEGMA, monomer) and poly(ethylene glycol) dimethacrylates (PEGDMAs, crosslinkers). The real-time crosslinking behavior of the PEG hydrogels was quantified as a function of the UV irradiation time and reaction temperature during the UV and thermal polymerization, respectively, using real-time FT-IR s
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