• Journal of the Korean institute of surface engineering
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• v.21 no.2
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• pp.53-67
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• 1988

The high temperature corrosion of Fe-C alloys were studied at I atm SO gas in the temperature range 500~80$0^{\circ}C$ by means of a thermogravimetric analysis. The Na2SO4 induced high tempwrature corrosion rate was also measured at atm O2 gas under above the temperature renge. The reaction products were identified with the aid of X-ray diffraction technique, and micostruction of the alloy/scale interface was observed with a optical microscope and SEM. The experimental results were disussed by the themodeynamic calcutions. Under above the experimental condition. the reaction rates decrbon with increasing carbon content. The transfer of Fe ion was limited by a residue of carbon precipitated at alloy scale interface due to the oxidation of Fe-C alloys at alloy surface. The effect of cold working on reaction rate was different between the Fe containing low carbon and Fe-C Alloy containing carbon above 0,73 wt%. In a cold worked iron containing low carbon content, the crystallization of metal surface leads to the poor adherence between the alloy and the cavity formed between the alloy and scale. The outward diffusion of ion through the scale is estimated to be hindered by the cavity formed between the scale, consequently decreasing reaction rate. In the case Fe-C containing carbon above 0.73 Wt% alloy, the reaction rate was little affected by cold working, because the effect of content on reaction rats is greater than the effect of cold working.

• Carbon letters
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• v.7 no.1
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• pp.1-8
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• 2006

The activated carbon "C" was obtained by carbonization followed by activation with steam at 40% of burn-off. Oxidized carbons C-N, C-P and C-H were obtained by oxidizing the activated carbon C with concentrated nitric acid, ammonium peroxysulfate and hydrogen peroxide, respectively. The textural properties of the carbons were determined from nitrogen adsorption at 77 K. The acidic surface functional groups were determined by pH titration, base neutralization capacity and electrophoretic mobility measurements. The cation exchange capacities of un-oxidized and oxidized carbons were determined by the removal of Cu(II) and Ni(II) from their aqueous solutions. The surface area and the total pore volume decreased but the pore radius increased by the treatment of activated carbon with oxidizing agents. These changes were more pronounced in case of oxidation with $HNO_3$. The surface pH of un-oxidized carbon was basic whereas those of the oxidized derivative were acidic. The removal of Cu(II) and Ni(II) was pH dependent and the maximum removal of the both ions was obtained at pH of 5-6. Cu(II) was more adsorbed, a phenomenon which was ascribed to its particular electronic configuration.

• Journal of Radiation Industry
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• v.3 no.1
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• pp.1-5
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• 2009

The variation of MgO surfaces, in which fluorine was contained (F-MgO), by high energy electron-beam (EB) was studied using X-ray photoelectron spectroscopy (XPS). Fluorine on the MgO surface was eliminated by EB treatment with the consequence that the electronic structures of Mg, O and C were varied. Moreover, as a result of oxidation of carbon species on the surface by high dose EB treatment (90 kGy), the concentration of carbonate and carboxyl species on the surface was increased. In this experiment, it was confirmed that the structure of oxidized metal surface can be adjusted by varying conditions of EB treatment (energy and dose). This result implies that EB can be applied for developing new catalysts.

• Carbon letters
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• v.9 no.1
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• pp.8-16
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• 2008

Oxidized activated carbons were prepared by reacting steam-activated carbon developed from pecan shells with nitric acid of varying strength (15, 30, 45 and 60%). The textural properties and the chemistry of the surface of the non-oxidized and of the oxidized carbons were determined from nitrogen adsorption and base neutralization capacities. The uptake of Pb(II) and Cd(II) from aqueous solution by these carbons was determined by kinetic and equilibrium experiments as well as by the column method. Treatment with nitric acid brought about drastic decrease in surface area and remarkable increase in the pore size of the carbon with these changes depending on the strength of nitric acid. Nitric acid increased the surface acidity by developing new surface oxygen functional groups of acidic nature. $HNO_3$-oxidized carbons exhibited high adsorption capacities for Pb(II) and Cd(II). The adsorption of these ions increased with the decrease of the surface pH of the carbon and with the increase of the solution pH from 2.5 to 6 and 7. The amount adsorbed from lead and cadmium was also related to the amount of surface acidity, the pH of the point of zero charge and on some metal ion parameters. Cadmium and lead uptake by the investigated carbons followed pseudo-second order model and the equilibrium sorption data fitted Langmuir adsorption model.

• Proceedings of the Korean Institute of Surface Engineering Conference
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• 2013.05a
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• pp.105-105
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• 2013

탄소 탄소 복합재료(C/C Composites)는 초고온 구조재료로서 모재의 성분이 탄소로 구성되어 있어 약 $500^{\circ}C$이상의 산화분위기에서는 쉽게 산화된다. 본 연구에서는 내산화성을 향상시키기 위한 방법으로서 SiC코팅층으로 내산화성코팅 층을 형성시킨 후 $1600^{\circ}C$에서 6시간동안 산화시험을 하였다.

• Proceedings of the Korean Institute of Surface Engineering Conference
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• 2012.05a
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• pp.201-201
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• 2012

탄소 탄소 복합재료(C/C composite)는 고온도 영역에서 강도저하가 없으며 화학적으로 더욱 안정되어 지기 때문에 고온 구조재료로서 널리 사용되어지고 있다. 모재의 성분이 모두 탄소로 구성되어 있어 약 $500^{\circ}C$의 산화분위기에서 부터는 산화되는 결점을 가지고 있다. 본 연구에서는 이러한 결점을 보완하기 위해 Pack Cementation과 Dipping 방법을 통해 내산화 코팅층을 형성 하여 $1300^{\circ}C$에서의 내산화성을 향상 시킬 수 있었다.

• Journal of the Korean Graphic Arts Communication Society
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• v.18 no.1
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• pp.71-81
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• 2000

The water-based ink has lately attracted considerable attention because of problems of energy and population. Carbon blacks have been widely utilized in water-based systems to provide pigmentation. One of the most important factors in the successful formulation of an aqueous system containing carbon black is the dispersion and the selection and proper utilization of the dispersing agent. This is similar to water-based ink. This paper discusses dispersion of carbon black with the factors affecting the dispersing agent requirement (DAR) and describes a laboratory method for determining it. Variables that affect the dispersion, such as structure, surface area, and oxidation level of the carbon black are examined through test data. Anionic and nonionic dispersing agents are evaluated using the DAR method. From this study, the increased surface area, the increased DAR is indicated. DAR is indicated to depend on HLB(Hydrophilic Lipophilic Balance) of dispersing agent and pH of dispersing system.

• Bulletin of the Korean Chemical Society
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• v.18 no.8
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• pp.814-818
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• 1997

The chemical waste treatment, APEG (alkali/polyethylene glycol) process has been shown to be effective for the dechlorination of PCBs in transformer oil. Considerable amount of PCBs, however, still remains in the waste exceeding the 25-50 ppm limit set by regulatory agency. A new thermal regeneration technology has been developed in our laboratory for disposal of hazardous organic wastes. Due to the limited oxidation of carbon surface through the reverse movement of flame front to oxidant flow, this technology was termed counterflow oxidative system (COS). Specially, the oxidant flow in the COS process is a principal parameter which determines the optimum conditions regarding acceptable removal and destruction efficiency of adsorbed organic wastes at minimal carbon loss. The COS process, under optimum conditions, was found to be very effective and the removal and destruction efficiency of 99.99% or better was obtained for residual PCBs in the waste while bulk (≥90%) of carbon was recovered. Any toxic formation of polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzo furans (PCDFs) were not detected in the regenerated carbon and impinger traps. The results of surface area measurement showed that the adsorptive property of regenerated carbon is mostly reclaimed during the COS process.

• Environmental Engineering Research
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• v.14 no.1
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• pp.32-40
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• 2009

In this study, we have prepared three kinds of carbon nanometer tube $CNT/TiO_{2}$ electrodes through impregnation with different concentration titanium n-butoxide (TNB) solution. The prepared electrodes were characterized with surface properties, structural crystallinity, elemental identification and photoelectrocatalytic activity. The $N_2$ adsorption data showed that the composites had decreased surface area compared with the pristine CNT. This indicated the blocking of micropores on the surface of CNT, which was further supported by observation via SEM. XRD results showed patterns for the composites and a typical single and clear anatase crystal structure. The main elements such as C, O and Ti were existed for all samples from the EDX data. The catalytic efficiency of the developed electrode was evaluated by the photoelectrodegradation of methylene blue (MB). The positive potential applied in photoelectrocatalytic (PEC) oxidation was studied. It was found that photoelectrocatalytic (PEC) decomposition of MB solution could be attributed to combination effects between $TiO_2$ photocatalytic and CNT electro-assisted. Through the comparison between photocatalytic (PC) oxidation and photoelectrocatalytic (PEC) oxidation, it was found that the PEC oxidation efficiency for MB is higher than that of PC oxidation.

• Journal of the Korean Society for Heat Treatment
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• v.14 no.2
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• pp.103-109
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• 2001

Plasma nitrocarburising and post oxidation were performed on SM45C steel using a plasma nitriding unit. Nitrocarburising was carried out with various methane gas compositions with 4 torr gas pressure at $570^{\circ}C$ for 3 hours and post oxidation was carried out with 100% oxygen gas atmosphere with 4 torr at different temperatures for various times. It was found that the compound layer produced by plasma nitrocarburising consisted of predominantly ${\varepsilon}-Fe_{2-3}(N,C)$ and a small proportion of ${\gamma}-Fe_4(N,C)$. With increasing methane content in the gas mixture, ${\varepsilon}$ phase compound layer was favoured. In addition, when the methane content was further increased, cementite was observed in the compound layer. The very thin oxide layer on top of the compound layer was obtained by post oxidation. The formation of Oxide phase was initially started from the magnetite($Fe_3O_4$) and with increasing oxidation time, the oxide phase was increased. With increasing oxidation temperature, oxide phase was increased. However the oxide layer was split from the compound layer at high temperature. Corrosion resistance was slightly influenced by oxidation times and temperatures.