• Journal of the Korean Society of Combustion
• /
• v.8 no.2
• /
• pp.27-33
• /
• 2003

Synthesis of carbon nanomaterials on a metal substrate by an ethylene fueled inverse diffusion flame was illustrated. Stainless steel plates were used for the catalytic metal substrate. The effects of catalyst metal particles were investigated through $Fe(NO_3){_3}$ (ferric nitrate, nonahydrate) and $Ni(NO_3){_2}$ (nickel nitrate, hexahydrate). Carbon nanotubes and nanofibers with diameters of $30{\sim}70nm$ were found on the substrate for the case of using SUS304 substrates only and using them with metal nitrates. In case of using metal nitrates, due to the easy activation of the metal particles, the formation and growth of carbon nanomaterials were occurred in the lower temperature region than that of using SUS304 substrates only.

• Carbon letters
• /
• v.9 no.2
• /
• pp.121-126
• /
• 2008

High modulus pitch based carbon fibers (HM) were exposed to isothermal oxidation using tube furnace in carbon dioxide gas to study the oxidation kinetics under the temperature of $800-1100^{\circ}C$. The kinetic equation $f=1-{\exp}(-at^b)$ was introduced and the constant b was obtained in the range of 1.02~1.42. The oxidation kinetics were evaluated by the reaction-controlling regime (RCR) depending upon the apparent activation energies with the conversion increasing from 0.2 to 0.8. The activation energies decrease from 24.7 to 21.0 kcal/mole with the conversion increasing from 0.2 to 0.8, respectively. According to the RCR, the reaction was limited by more diffusion controlling regime for the HM fibers with the conversion increasing. Therefore, it seems that the oxidation which is under the diffusion controlling regime takes place continuously from the skin to the core of the fiber.

• Journal of the Korean Institute of Electrical and Electronic Material Engineers
• /
• v.15 no.2
• /
• pp.147-152
• /
• 2002

Carbon nitride thin films were deposited by reactive sputtering for the hard coating materials on Si wafer and tool steels. When the nitrogen content of carbon nitride film on tool steel is 33.4%, the mean hardness and elastic modulus are 49.34 GPa and 307.2 GPa respectively. The nitrided or carburised surface acts as the diffusion barrier which shows better adhesion of carbon nitride thin film on the steel surface. To prevent nitrogen diffusion from the film, steel substrate can be saturated by nitrogen forming a Fe$_3$N layer. The desirable structure at the surface after carburising is martensite, but sometimes, due to high carbon content an proeutectoid Fe$_3$C structure may form at the grain boundaries, leaving the overall surface brittle and may cause defects.

• Carbon letters
• /
• v.1 no.1
• /
• pp.27-30
• /
• 2000

Performance of direct methanol fuel cell using high porous active carbon as an uncatalysed diffusion layer in anode (composite electrode) has been evaluated. Effects of porous active carbon in anode were investigated by galvanostatic method and Fourier Transform Infrared spectroscopy. The single cell was operated with 2.5 M methanol at temperature of $80-120^{\circ}C$ and showed performance of $210-510\;mA/cm^2$ at 0.4V. By replacing conventional electrode with composite electrode, the increment of $290\;mA/cm^2$ in current density was obtained at $90^{\circ}C$and 0.4V. The potential decay of the single cell was about 14.5% for 20 days operation.

• Proceedings of the KSME Conference
• /
• 2004.04a
• /
• pp.1304-1309
• /
• 2004

Synthesis of carbon nanotubes and nanofibers on a catalytic metal substrate, using an ethylene fueled inverse diffusion flame, was investigated. Multi-walled carbon nanotubes, with diameters of 20 - 60nm, were formed on the substrate coated with nickel-nitrate in the region of 5 - 6mm from the flame center along the radial direction. The gas temperature for this region was ranging from about 1400 to 900K. Nickel particles originated from the coated nickel-nitrate on the substrate were the major catalyst for the formation of the nanomaterials. HR-TEM and Raman spectrum revealed that synthesized carbon nanotubes had multi-walled structures with some defective graphite layers at walls.

• Journal of the Korea Concrete Institute
• /
• v.15 no.3
• /
• pp.443-453
• /
• 2003

The diffusivity of carbon dioxide in concrete is very important in that it directly affects the degree of carbonation in concrete structures. The purpose of the present study is to explore the diffusivity of carbon dioxide and to derive a realistic equation to estimate the diffusion coefficient of carbon dioxide in concrete. For this purpose, several series of concrete specimens have been tested. Major test variables were the water-cement ratios. The total porosities and the diffusion coefficients of carbon dioxide were measured for the specimens. The present study indicates that the measured porosities agree well with the calculated ones. The effects of porosity and relative humidity on the diffusion coefficient of carbon dioxide were examined. A prediction equation to estimate the diffusion coefficient of carbon dioxide was derived and proposed in this study. The proposed equation shows reasonably good correlation with test data on the $CO_2$ diffusion coefficient of concrete

• Korean Chemical Engineering Research
• /
• v.57 no.3
• /
• pp.358-367
• /
• 2019

Adsorption equilibrium and intraparticle diffusion characteristics of benzene, toluene, and xylene vapors on activated carbon and zeolite 13X were investigated. Static adsorption experiments were carried out under the pressure range of 0.01~0.07 bar while changing the adsorption temperature to 293.15 K, 303.15 K, and 313.15 K, respectively. Adsorption equilibrium was analyzed by Langmuir, Freundlich and Toth models. The adsorption energy was 5.26~31.0 kJ/mol representing physical adsorption characteristics. The maximum adsorption capacity on activated carbon was the largest for benzene, and the smallest for xylene. Toluene was in between. In the case of zeolite 13X, the maximum adsorption capacity was the largest for xylene, and the smallest for benzene as opposed to activated carbon. The effective diffusion coefficients of gas adsorbate were measured to be about $10^{-5}{\sim}10^{-4}cm^2/s$, and increased with temperature. As the pressure increased, the effective diffusion coefficients were decreased. The dependence of effective diffusion coefficients on temperature and pressure was greater in zeolite 13X particles than in activated carbon. Therefore, it is necessary to express the diffusion coefficients as a function of pressure in order to predict the precise dynamic behavior of the adsorption process using zeolite 13X where the pressure fluctuation occurs abruptly.

• Composites Research
• /
• v.12 no.6
• /
• pp.15-21
• /
• 1999

Carbon fibers were coated with carboxy modified poly(hydroxy ether)(C-PHE, water dispersed), water soluble polymers poly(hydroxy ether ethanol amine)(PHEA) or water insoluble poly(hydroxy ether)(PHE). Interfacial shear strength of polymer coated carbon fibers was measured by micro-droplet tests with vinyl ester resin, and approximately 30 samples were tested. The interfacial adhesion of poly-mers to carbon fibers was also evaluated, and diffusion behavior of polymer films in vinyl ester resin was investigated. The carbon fibers after testing and diffusion samples were analysed by SEM in order to understand adhesion mechanism. Interfacial shear strength of carbon fibers was enhanced by the coating of PHE and C-PHE which have good or marginal solubility in vinyl ester resin, respectively, but not by the coating of PHEA possibly due to the poor solubility in vinyl ester resin.

• Journal of the Korean Professional Engineers Association
• /
• v.20 no.4
• /
• pp.5-11
• /
• 1987

The experiment was carried out for the purpose of studying the carburization of pure iron ingot and sintered iron powder by solid carbon in the atmosphere of $N_2$ gas. The velocity of carburization was estimated by the diffusion coefficient D calculated by carburization equation. The results obtained were as follows ; 1. The briqueted sample of iron fine powder which made by higher pressure, carburization depth and carbon concentration were increased as much, and pure iron shelved the maximum value. 2, The higher the carburization temperature, carburization depth and carbon concentration were increased, and the melting zone which had 3.0~3.3%C at the interface of carburization was formed at 130$0^{\circ}C$. As the pure iron ingot was carburized, the diffusion coefficient D of carbon were 0.211$\times$$10^{-6}$$\textrm{cm}^2$ㆍsec$^{-1}$ at 120$0^{\circ}C$ and 0.391$\times$$10^{-6}$$\textrm{cm}^2$ㆍsec$^{-1}$ at 130$0^{\circ}C$, respectively. 4. As the sintered iron powder was carburized at the pressure of 4 ton/$\textrm{cm}^2$, the diffusion coefficient of carbon were 0.157$\times$$10^{-6}$$\textrm{cm}^2$ㆍsec$^{-1}$ at 120$0^{\circ}C$ and 0.103$\times$$10^{-5}$$\textrm{cm}^2$ㆍsec$^{-1}$ at 130$0^{\circ}C$, respectively.

• Bulletin of the Korean Chemical Society
• /
• v.32 no.3
• /
• pp.836-840
• /
• 2011

This study examines the effects of a carbon coating on the electrochemical performances of $LiFePO_4$. The results show that the capacity of bare $LiFePO_4$ decreased sharply, whereas the $LiFePO_4$/C shows a well maintained initial capacity. The Li ion diffusivity of the bare and carbon coated $LiFePO_4$ is calculated using cyclic voltammetry (CV) to determine the correlation between the electrochemical performance of $LiFePO_4$ and Li diffusion. The diffusion constants for $LiFePO_4$ and $LiFePO_4$/C measured from CV are $6.56{\times}10^{-16}$ and $2.48{\times}10^{-15}\;cm^2\;s^{-1}$, respectively, indicating considerable increases in diffusivity after modifications. The Li ion diffusivity (DLi) values as a function of the lithium content in the cathode are estimated by electrochemical impedance spectroscopy (EIS). The effects of the carbon coating as well as the mechanisms for the improved electrochemical performances after modification are discussed based on the diffusivity data.