• 한국분말야금학회:학술대회논문집
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• 한국분말야금학회 2006년도 Extended Abstracts of 2006 POWDER METALLURGY World Congress Part 1
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• pp.355-356
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• 2006

WC-TiC-TaC binderless cemented carbide was oxidized under low partial pressure of oxygen (50ppm) at 873K for 1 to 20 h. Surface roughness was measured using atomic force microscope, and effect of TiC amount on oxidation behavior of the carbide was investigated. WC phase was oxidized more easily than WC-TiC-TaC solid solution phase. With an increase in TiC amount, WC-TiC-TaC phase increased and the oxidation resistance of the carbide increased.

• Korean Chemical Engineering Research
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• 제62권4호
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• pp.364-370
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• 2024

In response to the threats of global warming and climate change, the development of highly energy-efficient lean methane oxidation processes has become crucial. One promising technology is ozone-induced lean methane oxidation (O₃-LMO), which utilizes ozone as an oxidant and a transition metal-loaded zeolite as a catalyst. Our previous study demonstrated that the O₃-LMO system, employing a cobalt-exchanged BEA (Co-BEA) catalyst, effectively abates lean methane (500 ppm) at low temperatures below 200℃ under dry conditions. In this study, we investigated the effect of water vapors on the performance of Co-BEA-based O₃-LMO system. The results indicated that CH₄ conversion, CO₂ selectivity, and O₃ utilization efficiency of the system were not significantly affected by water vapors. Additionally, any temporary suppression of activity could be easily reversed through simple vacuum drying of the catalyst. The system maintained robust activity for over 18 hours during prolonged testing under wet conditions.

• 한국환경과학회지
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• 제16권12호
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• pp.1431-1437
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• 2007

Cobalt titanates($CoTiO_x$), such as $CoTiO_3$ and $Co_2TiO_4$, have been synthesized via a solid-state reaction and characterized using X-ray diffraction(XRD) and X-ray photoelectron spectroscopic(XPS) measurement techniques, prior to being used for continuous wet trichloroethylene(TCE) oxidation at $36^{\circ}C$, to support our earlier chemical structure model for Co species in 5 wt% $CoO_x/TiO_2$(fresh) and(spent) catalysts. Each XRD pattern for the synthesized $CoTiO_3$ and $Co_2TiO_4$ was very close to those obtained from the respective standard XRD data files. The two $CoTiO_x$ samples gave Co 2p XPS spectra consisting of very strong main peaks for Co $2p_{3/2}$ and $2p_{1/2}$ with corresponding satellite structures at higher binding energies. The Co $2p_{3/2}$ main structure appeared at 781.3 eV for the $CoTiO_3$, and it was indicated at 781.1 eV with the $Co_2TiO_4$. Not only could these binding energy values be very similar to that exhibited for the 5 wt% $CoO_x/TiO_2$(fresh), but the spin-orbit splitting(${\Delta}E$) had also no noticeable difference between the cobalt titanates and a sample of the fresh catalyst. Neither of all the $CoTiO_x$ samples were active for the wet TCE oxidation, as expected, but a sample of pure $Co_3O_4$ had a good activity for this reaction. The earlier proposed model for the surface $CoO_x$ species existing with the fresh and spent catalysts is very consistent with the XPS characterization and activity measurements for the cobalt titanates.

• 한국재료학회지
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• 제13권12호
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• pp.831-838
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• 2003

Anisotropic mesophase carbon fiber(AMCFs) was exposed to isothermal oxidation in air and $CO_2$atmosphere, and burn-off rates have measured by TGA. The microstructure changes of oxidized carbon fibers, were observed by SEM. It was observed that oxidation rate in the air is over 100 times faster than that in $CO_2$atmosphere. The activation energy obtained in air was about 43.4 Kcal/mole in the temperature range of $600∼800^{\circ}C$, and in $CO_2$was about 55.2 Kcal/mole in the temperature range of $950∼1200^{\circ}C$. Therefore, the oxidation reaction in both atmospheres was under chemical reaction regime in the above temperature ranges. It was shown that the oxidation of the AMCFs is initiated at the end of fibers at high temperature($1100^{\circ}C$) with developing the large pores, and the small pores are developed on the fiber surface at low temperature($900^{\circ}C$). In conclusion, the oxidation of the AMCFs is progressed through the imperfection.

• 공업화학
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• 제23권3호
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• pp.253-258
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• 2012

본 연구는 $Pd/TiO_2$ 촉매를 이용한 $CH_4$, CO 동시 산화반응에서 활성점 및 Pd의 산화 상태에 대한 영향을 조사하였다. Pd 함량이 증가할수록 Pd 종(PdO)의 결정성장을 야기시켜 $CH_4$ 산화반응 활성을 증진시켰다. 열처리를 통해 제조된 촉매표면의 Pd 산화상태에 따라 $CH_4$과 CO의 산화반응 활성이 상이한 결과를 나타내었다. XRD와 $H_2-TPR$ 분석으로 소성촉매는 $Pd^{2+}$종, 환원촉매는 $Pd^0$종이 우점하고 있음을 확인하였다. 또한, BET분석을 통해 촉매 활성인자인 비표면적 및 기공부피보다는 Pd의 산화상태가 촉매 활성에 미치는 중요한 인자임을 알 수 있었다. FT-IR 분석을 이용하여 Pd의 산화상태에 따른 $CH_4$과 CO의 반응 메커니즘을 확인할 수 있었다.

• 공업화학
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• 제10권1호
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• pp.58-66
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• 1999

알루미나에 담지한 $CrO_x$ 촉매를 이용하여 $200{\sim}400^{\circ}C$의 온도 구간에서 공기 중 vinyl chloride의 산화반응을 조사하였다. 탄소를 포함하는 주생성물은 CO 및 $CO_2$로, 온도의 증가에 따라 $CO_2$의 선택도는 증가하고 CO는 감소하였다. 이로부터 $CrO_x$ 촉매상에서 vinyl chloride는 먼저 CO로 일차산화 후 다시 $CO_2$로 완전산화됨을 알 수 있었다. 반응물에 HCl을 첨가하였을 때 vinyl chloride의 전환율은 변화가 없었으나 $CO_2$의 선택도는 감소하였는데 이는 주반응생성물인 HCl이 vinyl chloride의 $CO_2$로 완전산화를 방해함을 의미한다. 반응물에 물이 없는 조건하에서 vinyl chloride를 산화시킬 때 상당량의 $Cl_2$가 생성되었으나 물을 첨가 시 $Cl_2$는 검출되지 않았다. Vinyl chloride의 촉매산화반응에 대한 $CrO_x$ 담지촉매와 몇가지 귀금속 및 다른 전이 금속 산화물의 활성을 비교하였는데 $CrO_x$ 담지촉매의 vinyl chloride 분해활성은 1% Pt 담지촉매를 제외한 다른 촉매에 비해 높았으며, $275^{\circ}C$에서 12% $CrO_x/Al_2O_3$의 반응속도를 기준으로 각 촉매의 활성을 비교시 1% $Pt/Al_2O_3$ 보다 1.2배정도 활성이 떨어지나 다른 촉매에 비하여 각각 3배에서 8배 가량 높은 활성을 나타내었다.

• Corrosion Science and Technology
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• 제19권1호
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• pp.43-50
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• 2020

In this study, the effects of KCl(s) and K₂SO₄(s) on the oxidation characteristics of 2.25Cr-1Mo steel were investigated for 500 h in 10O₂ + 10CO₂ (vol%) gas environmen at 650 ℃. Oxidation kinetics were characterized by weight gain, oxide layer thickness, and fitted models for the experiment data were proposed. The fitted models presented considerable agreement with the experimental data. The oxide layer was analyzed using the scanning electron microscope, optical microscope, and energy dispersive X-ray spectroscopy. The oxidation kinetics of 2.25Cr-1Mo steel with KCl and K₂SO₄ coatings showed significantly different oxidation kinetics. KCl accelerated the oxidation rate very much and had linear oxidation behavior. In contrast, K₂SO₄ had no significant effect, which had parabolic kinetics. The oxide layer was commonly composed of Fe₂O₃, Fe₃O₄, and FeCr₂O₄ spinel. KCl strongly accelerated the oxidation rates of 2.25Cr-1Mo steel in the high-temperature oxidation environment. Conversely, K₂SO₄ had little effect on the oxidation rates.

• 공업화학
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• 제29권6호
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• pp.657-662
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• 2018

본 연구에서는, $Pt/TiO_2$ 촉매의 물리화학적 특성이 CO 상온산화 반응에 미치는 영향을 조사하기 위하여 각기 다른 물리적 특성을 가지는 다양한 $TiO_2$ 지지체를 이용하여 $Pt/TiO_2$ 촉매를 제조한 후 평가하였다. 촉매의 물리화학적 특성을 조사하기 위하여 XPS, CO-chemisorption, BET, CO-TPD 분석을 수행하였다. 그 결과, active particle diameter가 작을수록, metal dispersion, surface area가 클수록 우수한 CO 상온산화 반응을 나타내었다. 이러한 물리적 특성은 active site의 수를 증진시켜 대상물질은 CO의 흡착량의 증가를 야기시켰다. 또한, $O_2$-consumption이 클수록 우수한 산소 전달 능력을 통해 보다 높은 CO 상온산화 반응활성을 나타내었다.

• 한국표면공학회지
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• 제53권1호
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• pp.22-28
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• 2020

In this study, manganese dioxide (MnO₂) nanoparticles were synthesized from KMnO₄ and MnCl₂·4H₂O without any dispersing agents and oxidant via ultra-high pressure homogenization process. We investigated various physicochemical properties and CO oxidation reactions of the MnO₂ nanoparticles as a function of the number of passes at 1,500 bar in a high pressure homogenizer nozzle. The observed X-ray diffraction patterns and scanning electron microscopy images revealed that the synthesized MnO₂ nanoparticles had a hexagonal structure and a uniform spherical shape. It was found from the Brunauer-Emmett-Teller measurements that the pore size of the MnO₂ nanoparticles ranged from 23.6 to 7.2 nm and their specific surface area ranged from 24 to 208 m²g^-1. In particular, it was confirmed from the measurements of CO conversion into CO₂ that CO oxidation reaction over the MnO₂ nanoparticles exhibited excellent catalytic activity at low temperatures below 100℃.

• 한국재료학회지
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• 제7권2호
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• pp.121-128
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• 1997

이방성과 등방성을 갖는 두 종류의 피치계 탄소섬유를 TGA장치를 이용하여 $CO_{2}$gas와 공기중에서 등온산화반응을 실시하였다. $CO_{2}$ gas보다 공기중에서의 산화가 훨씬 빠르게 일어났으며, $600^{\circ}C$공기중에서 등방성 T-10IS섬유는 이방성 HM-60섬유보다 23.9배나 빠른 산화속도를 보였다. 실험적으로 구한 활성화에너지를 저온에서 36-56Kcal/mole의 값을 가지며, 고온에서는 6-13Kcal/mole의 값을 나타내었다. 반응기구(zone 1,2,3)의 천이도는 T-10IS섬유보다 HM-60 섬유가 높았으며, 공기중에서보다 $CO_{2}$ gas분위기에서 더 높게 나타났다. SEM으로 관찰된 표면상변화로부터 탄소섬유의 산화반응은 섬유의 결함을 따라 진행된다는 것을 알 수 있었다.