• 공업화학
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• 제18권5호
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• pp.495-500
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• 2007

석탄가스화기의 내벽은 내화물로 구성되어 있다. 내화물의 침식은 가스화기 내화물의 수명 및 교체시기에 영향을 미치는 중요한 인자이다. 본 논문에서는 슬래그와의 반응에 의한 내화재의 미세구조의 변화를 침식화합물의 형성에 가장 큰 영향을 미치는 산화철 농도의 함수로 조사하였다. 산화철 농도가 낮은 KIDECO 탄 슬래그에 산화철을 첨가하여 정적 침식실험을 수행한 후 $(Fe,Cr)_3O_4$의 형성과 침투 슬래그에서의 Fe의 고갈 깊이를 측정하였다. 그리고 FactSage를 이용한 평형계산을 통하여 chromite 형성조건을 조사하고 실험 결과와 비교하였다. 고정된 온도인 $1550^{\circ}C$에서 약 10%의 산화철을 포함한 KIDECO 슬래그에서는 $(Fe,Cr)_3O_4$의 형성이 관찰되지 않았으나 산화철의 함량이 증가될수록 $(Fe,Cr)_3O_4$ 형성이 관찰되었으며, 경계면의 $(Fe,Cr)_3O_4$ 층의 두께가 증가하였고, 산화철의 고갈 깊이도 증가하였다. 또한 산화철의 양이 많아질수록 화학적 침식이 증가하면서 슬래그와 내화물의 경계가 모호해지는 것을 확인하였다. 슬래그-내화재 계의 평형계산은 슬래그의 산화철 농도가 증가할수록 가스화기 조업온도에서 chromite 형성 가능성이 높아짐을 보여주었다, 또한 내화물이 슬래그에 용해된 경우와 같이 $Cr_2O_3$가 낮은 농도로 존재할 때 chromite 형성이 가장 유리하였고, 산화철의 농도가 20% 이하에서는 슬래그와 내화물이 같은 양으로 존재하는 경우가 chromite 형성에 가장 불리하였다.

• 한국재료학회지
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• 제11권1호
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• pp.34-38
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• 2001

Fe-28%Al($Fe_3Al$)과 Fe-28%Al-4%Cr($Fe_3Al-4Cr$) 금속간화합물을 대기중 1073, 1273, 1473k의 온도에서 최고 17일까지 장시간 산화시켰다. $Fe_3Al-4Cr$의 산화저항은 근본적으로 $Fe_3Al$과 거의 비슷하거나, 약간 우수하였다. $Fe_3Al$ 위에 형성된 산화물은 거의 순수한 ${\alpha}-AL_2O_3$로만 구성되어 있었으며, $Fe_3Al-4Cr$ 위에 형성된 산화물은 약간의 Fe와 Cr 이온이 고용된 ${\alpha}-AL_2O_3$로 구성되어 있었다. 외부산화막을 형성하기 위해 모재원소의 외부확산에 의해 산화물-모재 계면에는 Kirkendall 기공이 존재하였다. $Fe_3Al(-4Cr)$ 표면에 형성된 산화막은 1273k가지는 비교적 얇고 치밀하였으나, 1473k에서 산화막의 박리와 함께 상대적으로 큰 무게증가가 발생하였다.

• Journal of Magnetics
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• 제14권4호
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• pp.147-149
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• 2009

We report the exchange bias in antiferromagnet/ferrimagnet $Cr_2O_3/Fe_3O_4$ core/shell nanoparticles. The magnetic field hysteresis curve for $Cr_2O_3/Fe_3O_4$ nanoparticles after field-cooling (FC) clearly showed both horizontal ($H_{EB}{\sim}$610 Oe) and vertical (${\Delta}M{\sim}$5.6 emu/g) shifts at 5 K. These shifts disappeared as the temperature increased toward the Neel temperature of $Cr_2O_3\;(T_N{\sim}$307 K). The $H_{EB}\;and\;{\Delta}M$ values were sharply decreased between the $1^{st}\;and\;the\;2^{nd}$ magnetic field cycles, and then slowly decreased with further cycling. These results are discussed in terms of the formation of single domains with pinned, uncompensated, antiferromagnetic spin and their evolution into multi-domains with cycling.

• 한국표면공학회지
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• 제52권5호
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• pp.246-250
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• 2019

Nano-multilayered $Cr_{25.2}Al_{19.5}Si_{4.7}N_{50.5}$ films were deposited on the steel substrate by cathodic arc plasma deposition. They were corroded at $900^{\circ}C$ in $Ar/1%SO_2$ gas in order to study their corrosion behavior in sulfidizing/oxidizing environments. Despite the presence of sulfur in the gaseous environment, the corrosion was governed by oxidation, leading to formation of protective oxides such as $Cr_2O_3$ and ${\alpha}-Al_2O_3$, where Si was dissolved. Iron diffused outward from the substrate to the film surface, and oxidized to $Fe_2O_3$ and $Fe_3O_4$. The films were corrosion-resistant up to 150 h owing to the formation of thin ($Cr_2O_3$ and/or ${\alpha}-Al_2O_3$)-rich oxide layers. However, they failed when corroded at $900^{\circ}C$ for 300 h, resulting in the formation of layered oxide scales due to not only outward diffusion of Cr, Al, Si, Fe and N, but also inward movement of sulfur and oxygen.

• 연구논문집
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• 통권29호
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• pp.141-149
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• 1999

Brazing of Fe-Cr-Al alloy was carried out at $1200^{\circ}C$ in vacuum furnace using nickel-based filler metals : BNi-5 powder(Ni-Cr-Si-Fe base alloy} and MBF-50 foil (Ni-Cr-Si-B). The effect of boron content on the stability of oxide scale on the brazed joint was investigated by means of cyclic oxidation test performed at $1050^{\circ}C$ and $1200^{\circ}C$. Apparently, the joints brazed with MBF-50 containing boron showed relatively stable oxidation rates compared to boron-free BNi-5 at both temperatures. However, it was considered that the slower weight loss of MBF-50 brazed specimen wasn’t resulted from the low oxidation rate but from the spallation of oxide layer. The oxide layer consisted of thick spinel oxide on the surface and $Al_2 O_3$ internal oxide layer along the interface between mother alloy and braze, the mother alloy was also eroded seriously by the formation of spinel oxides such as $FeCr_2 O_4$ and $NiCr_2 O_4$ on the surface, likely to be induced by the change of oxide forming mechanism due to diffusion of boron from the braze. On the contrary, the joint brazed with BNi-5 showed the good oxidation resistance during the cyclic oxidation test. It seems that the oxidation can be retarded by the formation of stable $Al_2 O_3$ layer at the surface.

• 자원리싸이클링
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• 제16권6호
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• pp.3-9
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• 2007

생활 폐기물은 대부분 유리류와 자기류뿐만 아니라 많은 양의 iron을 함유하고 있으며 약 $3{\sim}11%$에 달한다. 대부분의 iron은 Ni-Fe와 Ni-Cr-Fe 같은 합금으로 존재하거나, 부식방지와 광택을 위해 Ni와 Cr로 도금된 iron으로 존재하고 있기 때문에 소각로에서 소각될 경우 철 재품 표면에 심하게 파손된 $Fe_3O_4$층과 함께 $NiFe_2O_4$와 FeCr_2O_4$을 형성하게 되어 바닥재에 존재하게 되어 중금속산화물 층을 형성시킬 수 있다. iron은 자력이 매우 강해 자력선별에 의해 쉽게 선별되며 이러한 효과로 인해 중금속 산화물의 선별까지 얻을 수 있다. 또한 바닥재는 다양한 Ni와 Cr 산화물들을 함유하고 있으며, Ni와 Cr은 강자성을 띈 물질이기 때문에 자력선별에 의해 큰 영향을 받을 수 있다. 따라서 자력선별에 따른 Ni와 Cr의 거동에 대해 조사하였으며 그 밖의 다른 중금속(Cu, Pb, Cd, As)들의 거동 또한 확인해 보았다. 그 결과 Ni와 Cr은 약 $45{\sim}50%$의 선별율을 보였으며, Cu와 Pb는 $15{\sim}20%$을 나타냈다. 또한 자력선별 전과 후의 바닥재에 대해 Ni와 Cr의 용출량을 확인해본 결과 자력선별 후 바닥재의 용출량이 더 낮음을 확인할 수 있었다.

• 한국표면공학회지
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• 제27권1호
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• pp.3-11
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• 1994

Cyclic hot corrosion studies have been carried out on(82~94) wt. % Fe-(5, 10, 15) wt. % Cr alloys con-taining either (1, 3)wt. % of Si or Pt as minor alloying elements in molten salts of($Na_2SO_4$+NaCl) between 820 and $920^{\circ}C$. Si or Pt decreased corrosion rate with the most pronounced effect being observed for alloys having 15wt. %Cr. Especially, as Si or Pt contents are increased from 1 to 3 wt. %, improved corrosion resistance was obtained. The beneficial effect of Si addition is due to the presence of the Si-rich second phase along the grain boundaries as well as the formation of the protective $SiO_2$layer between substrates and oxide scale. The Pt addition also increased the corrosion resistance by enhancing the formation ($Cr_2O_3$+layers and by increasing the adherence of the oxide scale.

• 한국재료학회지
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• 제13권1호
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• pp.36-42
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• 2003

The oxidation behaviors of Y-Cr bilayer deposited on ferritic steel by magnetron-sputtering for application of the Fe-Cr alloys as interconnectors of planar-type solid oxide fuel cells (SOFCs) were studied. After oxidation at $800^{\circ}C$ for 40 hours, the major phase of $Y_2$$O_3$and the minor phase of $YCrO_3$, $Mn_{1.5}$ $Cr_{1.5}$ $O_4$and Cr$_2$SiO$_4$were formed in the Y/Cr bilayered samples, while the major phase of Cr$_2$O$_3$and the minor phase of $Y_2$$O_3$were formed as the major phase in the Cr/Y bilayered samples. The Log(ASR/T) that expresses electric resistance of the Y/Cr coated specimen with nonconducting $_Y2$$O_3$oxide showed high value of -2.80 Ω$\textrm{cm}^2$$K^{-1}$ / and that of the Cr/Y coated specimen with conducting $Cr_2$$O_3$oxide appeared to be -4.11 Ω$\textrm{cm}^2$$^{K}$ . The electric resistance of the Y/Cr coated specimen was largely increased due to the formation of high resistance oxide scales. However, the Cr/Y coated specimen did not show any increase in the electric resistance and had the long-term stability of oxidation because there was no formation of the secondary phases with low conductivity.

• 대한금속재료학회지
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• 제50권5호
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• pp.361-368
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• 2012

Fe-(10, 20, 30, 40) wt%Cr alloys were corroded in $Na_2SO_4$ salts ($m.p.=884^{\circ}C$) at $800{\sim}900^{\circ}C$ for 3-300 hrs. Their corrosion resistance increased with an increase in Cr content owing to the formation of slowly growing $Cr_2O_3$. During corrosion, $Na_2SO_4$ dissociated and reacted with the alloys to form $Cr_2O_3$ and $Fe_2O_3$. Since $Fe_2O_3$ dissolved fast into the salts, most of the scales consisted primarily of $Cr_2O_3$. Inside the scale, a small amount of sulfides also existed. The oxidation, dissolution and detachment of the formed scales occurred significantly.

• Applied Microscopy
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• 제45권3호
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• pp.177-182
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• 2015

The boiler tubes of X20CrMoV12.1 used in fossil-fired power plants were obtained and analyzed for the effect of water treatment on the steam corrosion-induced oxide scale in an effort to better understand the oxide formation mechanism, as well as pertinent method of maintenance and lifetime extension. The specimens were analyzed using various microscopy and microanalysis techniques, with focuses on the effect of water treatment on the characters of scale. X-ray diffraction analysis showed that the scales of specimens were composed of hematite ($Fe_2O_3$), magnetite ($Fe_3O_4$), and chromite ($FeCr_2O_4$). Electron backscatter diffraction analysis showed that the oxides were present in the following order on the matrix: outer $Fe_2O_3$, intermediate $Fe_3O_4$, and inner $FeCr_2O_4$. After all volatile treatment or oxygenated treatment, a dense protective $Fe_2O_3$ layer was formed on the $Fe_3O_4$ layer of the specimen, retarding further progression of corrosion.