Papers by Author: Chang Seop Lee

Abstract: This research was conducted to synthesize carbon nanofibers on C-fiber textiles by thermal CVD using Fe catalyst. The substrate which was a carbon textile consisting of non woven carbon fibers and attached graphite particles, was oxidized by nitric acid before the deposition process. Hydroxyl groups were created on the C-fiber textile due to the oxidization step. Fe (III) hydroxide was subsequently deposited on the oxidized surface of the C-fiber textile. To deposit ferric particles two different methods were tested: i) deposition-precipitation, ii) dip-coating. For the experiments using both type of catalyst deposition the weight ratio of Fe to C-fiber textile was also varied. Ferric particles were reduced to iron after deposition by using H₂/N₂ gas and CNFs were grown by flowing ethylene gas. Properties of carbon nanofibers created like this were analyzed through Scanning Electron Microscopy (SEM), Energy Dispersive Spectroscopy (EDS), N₂-sorption (BET), X-Ray Diffraction (XRD), and X-ray Photoelectron Spectoscopy (XPS). In the case of deposition-precipitation method the result shows that the diameter of carbon nanofibers grew up to 40~60nm and 30~55nm at which the weight ratios of Fe catalyst to C-fiber textiles are 1:30 and 1:70 respectively. If Fe particles were deposited by dip-coating method, the diameter of carbon nanofibers grew up to 40~60nm and 25~30nm for the ratios of Fe catalyst to C-fiber textiles 1:10 and 1:30.

Abstract: In this study, carbon nanofibers were synthesized on iron and copper catalysts by Chemical Vapor Deposition (CVD). Investigation was made with respect to variation on thickness and surface of fibers based on concentration of iron and copper. In order to prepare metal catalysts of respective synthesis, iron nitrate and copper nitrate were calculated in proportion to weight ratio and then dissolved into distilled water. Obtained catalyst precipitates were filtered and then dried for more than 24 hours at 110°C. Carbon nanofibers were composed by using ethylene gas of carbon source through CVD after pulverization of fully dried catalyst precipitates. Analysis through SEM was made in order to investigate structural characteristics of composed carbon nanofibers, and qualitative and quantitative analyses were conducted on elements through EDS. In addition, crystalline analysis was made on carbon nanofibers through XRD and Raman, and specific surface area measurement was carried on carbon nanofibers composed through BET.

Abstract: A series of cation exchanged Y-zeolites were prepared by exchanging cations with various alkali (M+, M= Li, Na, K, Cs) metals. The structural and catalytic properties of the alkali metal exchanged Y-zeolites have been investigated by a number of analytical techniques. Comparative elemental analyses were determined by an Energy Dispersive Spectroscopy X-ray (EDS), X-ray Photoelectron Spectroscopy (XPS), Inductively Coupled Plasma-Atomic Emission Spectroscopy (ICP-AES) and X-ray Fluorescence (XRF) before and after cation substitution. The framework and non-framework Al coordination and the Si/Al ratios of the Y-zeolites were investigated by MAS Solid-State Nuclear Magnetic Resonance (NMR) spectroscopy. The Al NMR spectra were characterized by two 27Al resonance signals at 12 and 59 ppm, indicating the presence of the non-framework and framework Al respectively. The intensities of these resonances were used to monitor the amount of the framework and non-framework Al species in the series of exchanged zeolites. The 29Si NMR spectra were characterized by four resonance signals at -79, -84, -90, and -95 ppm. Changing the alkali metal cations in the exchanged Y-zeolites significantly altered the extent of the octahedral/tetrahedral coordination and the Si/Al ratio. The Fourier Transform Infrared spectra of the CO2 adsorbed on to the exchanged Y-zeolites showed a low frequency shift, as the atomic number of the exchanged alkali metal increased. In addition, the catalytic activity of these samples for NOx reduction were tested in combination with a non-thermal plasma technique and interpreted based on the above structural and spectroscopic information.