Hyun Wook Jung
고려대학교 화공생명공학과 · 공학
Hyun Wook Jung 교수의 연구실은 주로 고분자 수지 및 수성 젤의 형성 거동, 특히 광중합 및 열중합을 통한 교차결합 메커니즘과 거품 구조 제어를 중심으로 연구를 진행하고 있습니다. 전기스핀닝 기반 나노섬유 제작, PEG 기반 상전이성 수지 및 pH 민감성 인터페닝 네트워크 수지의 설계 및 물성 제어에 초점을 맞추고 있으며, 자동차 코ating 등 실용적 응용 분야와도 연계된 저온 경화 기술 개발도 진행 중입니다. 특히 실시간 분석 기법(FT-IR, 레오메트리)을 활용한 반응 동역학 분석이 강점입니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
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