• 제목/요약/키워드: Fe-Cr

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석탄-바이오매스 혼소발전 분위기에서 Fe-Cr-W 강의 고온부식 연구 (Study of High Temperature Corrosion of Fe-Cr-W Steel in Coal-Biomass Co-firing Power Plant Environment)

  • 김민정;샤오샤오;이동복
    • 한국표면공학회지
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    • 제52권5호
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    • pp.251-257
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    • 2019
  • Fe-9Cr-2W steels were corroded at $600-800^{\circ}C$ for up to 100 hr in ($Na_2SO_4-K_2SO_4-Fe_2O_3$)-($CO_2-0.3%SO_2-6%O_2$) mixed gas. The poor condition samples formed thick oxide scales that consisted primarily of $Fe_2O_3$ as the major oxide and $Fe_3O_4$, FeO as the minor one through preferential oxidation of Fe. Fe-9Cr-2W steels corroded fast, forming thick and non-protective scale. The scale divided into the outer and inner layer, which consisted of the outer Fe-O layer and the inner (Fe,Cr)-O layer containing some (Fe,Cr)-S.

LiCl 및 LiCl-${Li_2}O$ 용융염에서 Fe-Ni-Cr 합금의 부식거동 연구 (A Study on the Corrosion Behavior of Fe-Ni-Cr Alloys in Molten Salts of LiCl and LiCl-${Li_2}O$)

  • 조수행;장준선;홍순선;신영준;박현수
    • 한국재료학회지
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    • 제10권7호
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    • pp.471-477
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    • 2000
  • Fe-Ni-Cr 합금의 용융염 부식거동을 $650~850^{\circ}C$ 온도범위에서 조사하였다. 용융염 LiCl에서 Cr을 포함하지 않는 KSA(Kaeri Superalloy)-1 합금은 Fe의 내부산화가 발생하고, Cr을 포함한 KSA-4, Incoloy 800H와 KSA-5는 LiCrO$_2$의 치밀한 보호막이 형성되었다. 혼합용융염 $LiCl-LiO_2$O에서 KSA-1은 Fe의 내부산화, KSA-4는 Cr의 내부산화가 발생하였고, Cr 농도가 높은 Incoloy 800H와 KSA-5는 $LiCrO_2$의 다공성 피 이 형성되었다. 혼합용융염 $LiCl-Li_2$O 에서는 Cr 농도의 증가에 따라 부식속도가 증가하였으며, 부식속도는 시간의존선을 8%Cr 이하의 합금에서는 포물선법칙, 8%Cr 이상의 합금에서는 직선법칙을 나타내었다. 이러한 현상은 Li$_2$O에 의한 보호성 산화물 $Cr_2O_3$의 염기성 용해기구로 설명할 수 있다.

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Cr(VI) removal using Fe2O3-chitosan-cherry kernel shell pyrolytic charcoal composite beads

  • Altun, Turkan;Ecevit, Huseyin
    • Environmental Engineering Research
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    • 제25권3호
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    • pp.426-438
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    • 2020
  • In this study, cherry kernel shell pyrolytic charcoal was synthesized (CKSC) and composite beads were obtained by blending this pyrolytic charcoal with chitosan and Fe2O3 nanoparticles (Fe-C-CKSC). Cr(VI) adsorption from aqueous solutions by Fe-C-CKSC composite beads and CKSC adsorbents was studied comparatively. The effects of Cr(VI) initial concentration, adsorbent dosage, contact time, pH and temperature parameters on Cr(VI) adsorption were investigated. Adsorption reached an equilibrium point within 120 min for CKSC and Fe-C-CKSC adsorbents. The maximum Cr(VI) removal was obtained at the initial pH value of 1.56 for CKSC and 2.00 for Fe-C-CKSC. The optimum adsorbent dosage was found to be 5 g/L for CKSC and 3 g/L for Fe-C-CKSC. Based on the Langmuir model, the maximum adsorption capacities were calculated as 14.455 mg/g and 47.576 mg/g for CKSC and Fe-C-CKSC, respectively. Thermodynamic and kinetic studies were performed. As a result of adsorption kinetics calculations, adsorption was found to be consistent with the pseudo second order kinetic model. Characterization of the synthesized adsorbents was performed by SEM, BET, FTIR and elemental analysis. This study has shown that low cost adsorbents CKSC and Fe-C-CKSC can be used in Cr(VI) removal from aqueous solutions.

High-Temperature Oxidation of Ti Containing Stainless Steel in O2-N2 Atmosphere

  • Onishi, Hidenori;Saeki, Isao;Furuichi, Ryusaburo;Okayama, Toru;Hanamatsu, Kenko;Shibayama, Tamaki;Takahashi, Heishichiro;Kikkawa, Shinichi
    • Corrosion Science and Technology
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    • 제3권4호
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    • pp.140-147
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    • 2004
  • High temperature oxidation of Fe-19Cr and Fe-19Cr-0.2Ti alloys is studied at 1173-1373 K in 16.5 kPa $O_2$ - balances $N_2$ atmosphere aimed at clarifying the effect of titanium addition. Oxidation rate of Fe-19Cr alloy was accelerated with titanium. For both alloys chromium rich $(Fe,\;Cr)_2O_3$ was formed as a major oxidation product. On Fe-19Cr-0.2Ti alloy, a thin layer composed of spinel type oxide and titanium oxide was also formed and an internal oxidation of titanium was observed. Titanium was concentrated at the oxide surface and internal oxidation zone but a small amount of titanium was also found in the intermediate corundum type $(Fe,\;Cr)_2O_3$ layer. Crystals of corundum type $(Fe,\;Cr)_2O_3$ formed on Fe-19Cr alloy are coarse but that formed on Fe-19Cr -0.2Ti alloys were fine and columnar. Reason for the difference in oxidation kinetics and crystal structure will be discussed relating to the distribution of aliovalent titanium in corundum type $(Fe,\;Cr)_2O_3$ oxide layer.

수소제조를 위한 다공성 FeCrAl 금속 합금 Foam의 NiO 촉매 담지 및 미세구조 분석 (Synthesis and Microstructure Analysis of NiO Catalysts Coated on the FeCrAl Metal Alloy Foam for Hydrogen Production)

  • 이유진;안건형;박만호;이창우;최상현;정주용;조성종;이근재;안효진
    • 한국재료학회지
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    • 제24권8호
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    • pp.393-400
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    • 2014
  • NiO catalysts were successfully coated onto FeCrAl metal alloy foam as a catalyst support via a dip-coating method. To demonstrate the optimum amount of NiO catalyst on the FeCrAl metal alloy foam, the molar concentration of the Ni precursor in a coating solution was controlled, with five different amounts of 0.4 M, 0.6 M, 0.8 M, 1.0 M, and 1.2 M for a dip-coating process. The structural, morphological, and chemical bonding properties of the NiO-catalyst-coated FeCrAl metal alloy foam samples were assessed by means of field-emission scanning electron microscopy(FESEM), scanning electron microscopy-energy dispersive spectroscopy(SEM-EDS), X-ray diffraction(XRD), and X-ray photoelectron spectroscopy(XPS). In particular, when the FeCrAl metal alloy foam samples were coated using a coating solution with a 0.8 M Ni precursor, well-dispersed NiO catalysts on the FeCrAl metal alloy foam compared to the other samples were confirmed. Also, the XPS results exhibited the chemical bonding states of the NiO phases and the FeCrAl metal alloy foam. The results showed that a dip-coating method is one of best ways to coat well-dispersed NiO catalysts onto FeCrAl metal alloy foam.

연 X선 방사광 분광법을 이용한 TCr2O4(T = Fe, Co, Ni) 스피넬 산화물의 전자구조 연구 (Investigation of Electronic Structures of TCr2O4 (T = Fe, Co, Ni) Spinel Oxides by Employing Soft X ray Synchrotron Radiation Spectroscopy)

  • 김현우;황지훈;김대현;이은숙;강정수
    • 한국자기학회지
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    • 제23권5호
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    • pp.149-153
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    • 2013
  • 이 연구에서는 방사광 연 X선 광흡수 분광법(soft x-ray absorption spectroscopy: XAS)을 이용하여 $TCr_2O_4$(T = Fe, Co, Ni) 스피넬 산화물들의 전자 구조를 연구하였다. 전이금속 이온들의 2p 준위의 흡수에 의한 XAS 측정으로부터 T(T = Fe, Co, Ni) 이온들의 원자가는 공통적으로 2가($T^{2+}$)이며, Cr 이온의 원자가는 3가 ($Cr^{3+}$) 임을 발견하였다. 그리고 T 이온들은 정사면체 대칭성을 가진 A 사이트에 주로 위치하고, Cr 이온은 정팔면체 대칭성을 가진 B 사이트에 주로 위치함을 알 수 있었는데, 이러한 발견을 통하여 $TCr_2O_4$는 정상 스피넬에 가까운 구조를 가지고 있다고 결론지을 수 있다. 또한 $FeCr_2O_4$$NiCr_2O_4$에서는 얀-텔러 변형이 중요한 역할을 하지만, $CoCr_2O_4$는 얀-텔러 변형이 없는 입방체 구조를 유지하는 원인을 알 수 있었다. 그러므로 $TCr_2O_4$에서 $Cr^{3+}$ 상태의 이온들과 $T^{2+}$ 상태의 이온들 간의 반강자성 결합이 이 산화물들의 자성 특성을 결정하는데 중요한 역할을 한다고 생각된다.

생활폐기물(生活廢棄物) 소각(燒却) 바닥재의 자력선별(磁力選別)에 따른 크롬과 니켈의 거동(擧動) (Effect of magnetic separation in removal of Cr and Ni from municipal solid waste incineration (MSWI) bottom ash)

  • 안지환;엄남일;조계홍;오명환;유광석;한기천;조희찬;한춘;김병곤
    • 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 $NiFe_2O_4$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.

Fe-30at.%A1 합금의 압연성에 미치는 Cr, B, Ti 및 Si 첨가효과 (Effects of Cr, B, Ti and Si on Rolling Characteristics in Fe-30at.%A1 Alloy)

  • 최답천;이지성
    • 한국주조공학회지
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    • 제23권2호
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    • pp.77-85
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    • 2003
  • Some alloying elements such as Cr, B, Ti and Si were added individually or as a mixture to Fe-30 at.%Al alloys. The alloys were melted using an arc furnace and then heat-treated for homogenization at 1000$^{\circ}C$ for 7 days and followed by rolling at 1000$^{\circ}C$. The alloying elements on rolling characteristics were investigated by the microstructures and fracture mode before and after rolling. The microstructures before rolling showed that all of the alloys had equiaxed grains. On the other hand, the microstructures of rolling plane as well as its perpendicular plane became elongated after rolling. The alloys such as Fe-30Al, Fe-30Al-3Ti, Fe-30Al-0.5B, Fe-30Al-5Cr and Fe-30Al-3Ti-0.5B revealed better rolling behaviour from the point that intergranular and cleavage fractures were not fundamentally occurred. But the addition of 5Ti or 3Si to Fe-Al alloys had detrimental effects. The Ti-added alloy system such as Fe-30Al-5Ti, Fe-30Al-5Ti-5Cr, Fe-30Al-3Ti-5Cr and Fe-30Al-5Ti-0.5B were cracked through grain and showed cleavage fracture. The Si-added alloy system such as Fe-30Al-5Si, Fe-27Al-3Si and Fe-27Al-5Cr-3Si were cracked along the grain boundary and showed intergranular fracture. $DO_3{\leftrightarrow}B_2$ transition temperature of Fe-30at.%Al alloy was 520$^{\circ}C$, whereas the addition of 3Ti and 3Ti+0.5B comparably increased the temperature to 797 and 773$^{\circ}C$, respectively.

FeSiCr에 Fe50Ni가 첨가된 폴리머 복합 시트의 전자파 흡수 특성 (Electromagnetic Wave Absorbing Properties of FeSiCr and Fe50Ni Flaky Powder-Polymer Composite Sheet)

  • 이석문;김상문
    • 한국전기전자재료학회논문지
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    • 제27권7호
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    • pp.462-467
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    • 2014
  • In this paper, we studied the magnetic composite sheets for electromagnetic wave noise absorber of quasi-microwave band by using soft magnetic FeSiCr and Fe50Ni flakes with the thickness of about $1{\mu}m$ and polymer. The magnetic hysteresis curve including saturation magnetization and residual magnetization and the complex permeability characteristics of the composite sheets were investigated to clarify the mixing effect on electromagnetic wave absorption properties. The saturation magnetization was decreased about 10% while the residual magnetization was increased about 15% and the real parts of complex permeability at below 500 MHz were increased 0.6~4 while those values at above 500 MHz were decreased 0.4~2.5 according to the change of contents of FeSiCr and Fe50Ni powders. As a result, the reflection loss can be moved to the lower frequency from 2~3 GHz to 1~1.5 GHz as the contents of Fe50Ni flaky powder into FeSiCr flaky powder was increased up to 50%.

Effect of Al on Structural and Magnetic Characteristics of CoCrFeNiMnAlx High Entropy Alloys

  • Majid Tavoosi;Ali Ghasemi;Gholam Reza Gordani;Mohammad Reza Loghman Estarki
    • 한국재료학회지
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    • 제33권3호
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    • pp.95-100
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    • 2023
  • This research examines the effect of adding aluminum on the structural, phasic, and magnetic properties of CoCrFe NiMnAlx high-entropy alloys. To this aim, the arc-melt process was used under an argon atmosphere for preparing cast samples. The phasic, structural, and magnetic properties of the samples were characterized by x-ray diffraction (XRD), scanning electron microscopy (SEM), and vibrational magnetometry (VSM) analyses. Based on the results, the addition of aluminum to the compound caused changes in the crystalline structure, from FCC solid solution in the CoCrFeNiMn sample to CoCrFeNiMnAl BBC solid solution. It was associated with changes in the magnetic property of CoCrFeNiMnAlx high-entropy alloys, from paramagnetic to ferromagnetic. The maximum saturation magnetization for the CoCrFeNiMnAl casting sample was estimated to be around 79 emu/g. Despite the phase stability of the FCC solid solution with temperature, the solid solution phase formed in the CrCrFeNiMnAl high-entropy compound was not stable, and changed into FCC solid solution with temperature elevation, causing a reduction in saturation magnetization to about 7 emu/g.