• 연구논문집
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• 통권34호
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• pp.139-146
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• 2004

In this study, effect of temperature and time on melt-out of 25wt% Al-alloyed ductile iron has been investigated. The oxidation tests were carried out in a tube furnace at $800^\circC$, $930^\circC$, and $1000^\circC$ for lh, 5h, 10h, 50h. The microstructure, microhardness, and $Al_2O_3$ layer of oxidation-treated 25wt% Al-alloyed ductile iron samples (10 x 10 x 10 mm) were investigated. Phase identification was performed by X-ray diffraction(XRD) and EDS. The oxidation-treated 25wt% Al-alloyed ductile iron samples at $930^\circC$ for lh, 5h, 10h and KS GCD 500 were used for melt-out test in an Al alloy melt. The melt-out test results showed that oxidation tested sample at $930^\circC$ for 5h which on the whole forms $2-3\mum$ $Al_2O_3$ layer showed lowest melt-out depth. It was observed showed that appropriate Al203 layer can affect melt-out behaviors.

• The Korean Journal of Ceramics
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• 제5권3호
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• pp.211-216
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• 1999

Four different $\beta-Si_3N_4$ ceramics with silicon oxynitrides $[Y_10(SiO_4)_6N_2, Yb_4Si_2N_2O_7, Er_2Si_3N_4O_3, \;and La_{10}(SiO_4)_6N_2$, respectivley] as secondary phases have been fabricated by hot-pressing the $Si_3N_4-Re_4Si_2N_2O_7$ (Re=Y, Yb, Er, and La) compositions at $1820^{\circ}C$ for 2h under a pressure of 25 MPa. The high temperature strength and oxidation behavior of the hot-pressed ceramics were characterized and compared with those of the ceramics fabricated from $Si_3N_4-Si_2O_7$ compositions. The $Si_3N_4-Re_4Si_2N_2O_7$composition investigated herein showed comparable high temperature strength to those from $Si_3N_4-Re_2Si_2O_7$ compositions. Si3N4 ceramics from a $Si_3N_4-Y_4Si_2N_2O_7$ composition showed the highest strength of 877 MPa at $1200^{\circ}C$ among the compositions. All $Si_3N_4$ ceramics investigated herein showed a parabolic weight gain with oxidation time at $1400^{\circ}C$ and the oxidation products of the ceramics were $SiO_2$ and $Re_2Si_2O_7$. The $Si_3N_4-Re_4Si_2N_2O_7$ compositions showed inferior oxidation resistance to those from $Si_3n_4-Re_2Si_2O_7$ compositions, owing to the incompatibility of the secondary crystalline phases of those ceramics with $SiO_2$, the oxidation product of Si3N4.Si3N4 ceramics from a $Si_3N_4-Er_4Si_2N_2O_7$ composition showed the best oxidation resistance of 0.375mg/$\textrm{cm}^2$ after oxidation at $1400^{\circ}C$ for 102 h in air among the compositions.

• Korean Chemical Engineering Research
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• 제48권6호
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• pp.776-783
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• 2010

수소생산을 위한 메탄의 부분산화용 촉매로 알루미나에 담지된 코발트와 니켈 촉매를 함침법으로 제조하였다. 메탄의 부분산화반응을 위한 이들 촉매의 반응활성은1기압, $CH_4/O_2=2.0$과 $450{\sim}650^{\circ}C$의 온도영역에서 조사하였다. 담지량이 다른 코발트촉매와 니켈촉매의 반응활성을 비교하고 코발트촉매에 니켈을 첨가한 이성분금속 촉매의 반응활성을 조사하였다. 그리고 코발트촉매와 니켈촉매에 첨가된 Ce와 La의 첨가효과를 조사하였다. 이들 촉매의 특성은 XRD와 SEM/EDX로 분석하였다. 코발트와 니켈은 10 wt%의 담지량이 적절한 것으로 나타났다. 이들 10 wt% 담지 코발트와 니켈촉매는 열역학적 평형값에 가까운 메탄의 전환율과 CO의 선택성을 나타내었으나 $H_2$의 선택성은 평형값보다 다소 낮게 나타났다. 코발트촉매에 니켈을 첨가한 이성분금속 촉매에서 $H_2$의 선택성은 증가하였으나 전환율을 고려하면 니켈을 첨가한 이점은 나타나지 않았다. 코발트촉매에서는 Ce의 첨가와 니켈촉매에서는La의 첨가로 메탄의 전환율과 수소의 선택성을 높일 수 있었다.

• Korean Chemical Engineering Research
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• 제51권3호
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• pp.319-324
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• 2013

합성가스를 생산하기 위한 메탄의 부분산화반응 특성을 $Ni/CeO_2-ZrO_2$, $Ni-Ru/CeO_2-ZrO_2$와 $Ni-Pd/CeO_2-ZrO_2$ 촉매체를 이용하여 조사하였다. 메탄의 부분 산화 개질 반응에서 촉매의 높은 활성과 안정성을 위하여 허니컴 구조의 금속모노리스 촉매 체를 적용하였다. 촉매분석은 XRD와 FE-SEM을 사용하였으며, 제조된 촉매들의 합성가스 제조 특성은 반응물 비(O/C), GHSV와 온도를 변화시키면서 연구하였다. 개질 실험에서 사용된 촉매 중에서 $Ni-Pd/CeO_2-ZrO_2$ 촉매 체가 가장 높은 활성을 보여 주었으며, $900^{\circ}C$, GHSV=10,000 $h^{-1}$과 O/C=0.55에서 99%의 메탄 전환율을 얻었다. O/C 비가 증가함에 따라 수소 yield는 증가되고, 반면에 CO yield는 거의 일정하게 유지됨을 확인할 수 있었다. 또한 GHSV가 증가할수록 메탄의 전환율은 감소하였으며, 높은 메탄의 전환율을 얻을 수 있는 GHSV의 범위는 10,000 $h^{-1}$ 이하임을 알 수 있었다.

• Corrosion Science and Technology
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• 제12권3호
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• pp.119-124
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• 2013

Nano-multilayered, crystalline AlTiSiN thin films were deposited on WC-TiC-Co substrates by the cathodic arc plasma deposition. The deposited film consisted of wurtzite-type AlN, NaCl-type TiN, and tetragonal $Ti_2N$ phases. Their oxidation characteristics were studied at 800 and $900^{\circ}C$ for up to 20 h in air. The WC-TiC-Co oxidized fast with large weight gains. By contrast, the AlTiSiN film displayed superior oxidation resistance, due mainly to formation of the ${\alpha}-Al_2O_3$-rich surface oxide layer, below which an ($Al_2O_3$, $TiO_2$, $SiO_2$)-intermixed scale existed. Their oxidation progressed primarily by the outward diffusion of nitrogen, combined with the inward transport of oxygen that gradually reacted with Al, Ti, and Si in the film.

• 한국표면공학회:학술대회논문집
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• 한국표면공학회 2014년도 추계학술대회 논문집
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• pp.117-117
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• 2014

Thin $ZrO_2/Al_2O_3$ films were deposited on a tool steel substrate using Zr and Al cathodes in a cathodic arc plasma deposition system (CAPD), and then oxidized at $600-900^{\circ}C$ in air for up to 50 h. They effectively suppressed the oxidation of the substrate up to $800^{\circ}C$ by acting as a barrier layer against the outward diffusion of the substrate elements and inward diffusion of oxygen. However, rapid oxidation occurred at $900^{\circ}C$ due mainly to the increased diffusion and subsequent oxidation of steel as well as the crystallization of amorphous $Al_2O__3$.

• Bulletin of the Korean Chemical Society
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• 제23권6호
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• pp.799-803
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• 2002

Partial oxidation of methane has been conducted over $CeO_2$and it has been found that $CeO_2$has an extraordinary catalytic activity in the reaction. Its activity was strongly dependent on the $CH_4/CO_2$ ratio. Total combustion was dominant with stoichiometric feed ratio$(CH_4/O_2=$ 2.0) but partial oxidation was achieved between the $CH_4/O_2$ ration of 3.8 4.3 and the period depended upon the feed composition. The proposed raaction mechanism it that oxygen vacancies in raduced deria are supplied with oxygen molecules from the reactant, and then activate adsorbed oxygen, followed by releasing activated axygen species reacting with methane to produce $H_2$ and CO.

• 공업화학
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• 제22권6호
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• pp.617-622
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• 2011

축산폐수 혐기소화 유출수 중의 생물학적 난분해성 유기물의 분해를 위하여 오존 기반의 고도산화 기술을 적용하였다. 배출수의 COD 및 색도는 각각 9200~9500 mg/L 및 0.384 (400 nm)이고 1/10 희석하여 실험에 사용하였다. 공급 오존은 버블의 크기가 $13{\mu}m$인 마이크로버블 오존과 $105{\mu}m$인 일반 오존버블과의 차이를 고찰하였다. 마이크로버블 오존을 사용함으로써 오존의 용해도와 라디칼 생성량이 증가되었고 일반 오존버블에 비하여 COD 및 색도의 제거효율이 각각 85% 및 26% 향상되었다. 마이크로버블을 포함한 $O_3/UV$, $O_3/H_2O_2$, $O_3/UV/H_2O_2$의 조합을 비교한 결과 오존 단독 처리에 비하여 색도 제거율이 5~10% 정도 증가되었으며, 오존에 비하여 UV나 $H_2O_2$의 색도제거에 대한 기여가 크지 않음을 알 수 있었다. 반면 COD에 대해서는 $O_3/UV/H_2O_2$ 적용시 오존 단독에 비하여 2배 이상 제거율이 증가하였으며 UV보다는 $H_2O_2$의 기여도가 더 컸다. 한편 마이크로 오존의 사용시 증가된 용존오존 및 라디칼 활성으로 인하여 오존 공급을 중단한 후에도 UV 또는 $H_2O_2$를 적용함으로써 추가적인 COD 분해 효과를 지속적으로 유지할 수 있었다.

• 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.

• Corrosion Science and Technology
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• 제2권3호
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• pp.148-154
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• 2003

The addition of Ni leads to the formation of protective rust layer on steel and subsequently high corrosion resistance of steel in $Cl^-$-containing environment. $\alpha$-FeOOH, $\beta$-FeOOH, $\gamma$-FeOOH and $Fe_3O_4$ are formed mainly on steels exposed to $Cl^-$-containing environment. As the first work of this kind, this study reports the influence of Ni on the oxidation behavior of $Ni_xFe_{1-x}(OH)_2$ in $Cl^-$-containing solution at two different pH regions(condition I under which the solution pH is allowed to decrease and condition I under which solution pH is maintained at 8) where $\gamma$-FeOOH and $Fe_3O_4$ are predominantly formed, respectively, upon oxidation of $Fe(OH)_2$, In the presence of Ni(II) in the starting solution, the formation of $\beta$-FeOOH was facilitated and the formation of $\gamma$-FeOOH was suppressed with increasing Ni(II) content and with increasing oxidation rate of Fe(II). Ni(II) was found to have $Fe_3O_4$-suppressing effect under condition II.