• 제목/요약/키워드: $CrO_3$

검색결과 1,384건 처리시간 0.026초

$H_2/O_2$ 비에 따른 Hybrid HVOF 용사된 $Cr_3C_2$-7wt%(NiCr) 용사층의 특성 및 산화거동 (Characteristics and oxidation behavior of the hybrid-HVOF sprayed $Cr_3C_2$-7wt%(NiCr) coatings depending on $H_2/O_2$ ratio)

  • 김병희;서동수
    • Journal of Welding and Joining
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    • 제15권4호
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    • pp.126-135
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    • 1997
  • $H_2/O_2$ 비에 따른 Hybrid HVOF 용사된 $Cr_3C_2$-7wt%(NiCr) 용사층의 특성 및 산화거동 This study was performed to investigate the influence of fuel/oxygen ratio (F/O=3.2, 3.0, 2.8) on the characteristics and the oxidation behavior of the hybrid-HVOF sprayed $Cr_3C_2$-7wt%NiCr coatings. Decomposition and the oxidation of the $Cr_3C_2$was occured during spraying. The degree of transformation from $Cr_3C_2$to $Cr_7C_3$ was increased with decreasing the F/O ratio. The microstructural differences of the as sprayed coating with F/O ratio can not be distinguished, However, large pores were diminished and then the coatings became dense by heat treatment. Microhardness of the as-sprayed specimen which sprayed with F/O=3.0 condition was hightest ($Hv_{300}$=1140) and the hardness was increased to 1500 after heat treatment at $600^{\circ}C$ for 50hrs in air. It was supposed that hardness was increased due to the formation of $Cr_2O_3$ within $Cr_3C_2$/$Cr_7C_3$matrix and the densification of coating layer during heat treatment. Apparent activation energy for oxidation was varied from 21.2 kcal$mol^{-1}K^{-1}$ to 23.8 kcal$mol^{-1}K^{-1}$ with respect to the F/O ratio. The surface morphology was changed to porous and oxide chusters were grown after oxidation $1000^{\circ}C$ for 50 hours by the aggressive evolution of gas phase ($CrO_3$ and$CO_2$). The oxide cluster was composed of Ni and Cr.

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수소크롬산 이온에 의한 옥살라토아쿠아몰리브덴(IV) 삼합체의 산화반응 (Kinetic Studies on the Oxidation of Oxalatoaquamolybdenum(IV) Trimer by Hydrogen Chromate Ion)

  • 김창수;권창룡
    • 대한화학회지
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    • 제30권1호
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    • pp.57-62
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    • 1986
  • HCr$O_4^-$에 의한 $[Mo_3O_4(C_2O_4)_3(H_2O)_3]^{2-}$의 산화는 몰리브덴(IV)화합물, $[Mo_2O_5(C_2O_4)_2(H_2O)_2]^{2-}$를 생성한다. HCr$O_4^-$$[Mo_3O_4(C_2O_4)_3(H_2O)_3]^{2-}$의 반응에 대한 화학양론은 $2Mo_3^{IV} + 4Cr^{VI} {\to} 3Mo_2^{VI} + 4Cr^{III}$와 같다. 관찰된 속도상수는 수소이온농도에 의존한다.$Cr^{VI}$$Cr^V$$Cr^{IV}$를 거쳐서 $Cr^{III}$로 일전자씩 연속적으로 변화한다. 상세한 메카니즘이 논의된다.

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Sphene-Pink 안료에 미치는 CrCl3의 영향 (Influence of CrCl3 in Sphene-Pink Pigments)

  • 이현수;이병하
    • 한국세라믹학회지
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    • 제45권5호
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    • pp.268-275
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    • 2008
  • In high temperature ceramic glazes, a stable range of pink-red colors producing $Cr_2O_3-SnO_2-CaO-SiO_2$ pigments are factored by Cassiterite and Malayaite relationship with $Cr_2O_3$. The experiment described the effect of $CrCl_3$ by adding $H_3BO_3$ as a mineralizer to increase the formation of Malayaite crystal, substituting $CrCl_3$ instead of $Cr_2O_3$ in pigment as a chromophore. Synthesized pigments were analyzed by XRD, FT-IR, Raman Spectroscop, UV and UV-vis. The result shows the differences in amount of crystal phases and oxidation state of Cr ion, which causes the color change. The melting point of $CrCl_3$ is lower than $Cr_2O_3$ which act as a mineralizer and makes the pigment synthesized in lower temperature at $1200^{\circ}C$. Holding 3 h firing at $900^{\circ}C$ where the synthesize forms shows better effect of Malayaite crystal phases and increasing engaged effect of $CrCl_3$ where the color pigmentation is more defined then in $Cr_2O_3$.

$LaCrO_3$가 분산된 Cr 합금의 구조 및 산화거동 (Structure and Oxidation Behavior of the $LaCrO_3$-dispersed Cr alloys)

  • 전광선;송락현;신동열;조중열
    • 대한전기학회:학술대회논문집
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    • 대한전기학회 1998년도 하계학술대회 논문집 D
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    • pp.1303-1305
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    • 1998
  • In order to reduce or avoid oxidation problem at operation the interconnects in SOFCs have so far mostly been made of ceramic material. It has high chemical stability both under cathode and anode condition, relatively thermal expansion coefficient that matchs that of electrolyte material YSZ. But this material shown rather weak in the low oxygen atmosphere and thermal shock, and it has lower mechanical strength than alloys. To avoid these problems one may consider to use metals or alloys as materials for interconnects. Metallic interconnects are advantageous because of their high thermal and electronic conductivities. But it has some problems, Those are high thermal expansion and oxidation at high temperature in air. To solve these problems in the interconnection material in this study, $LaCrO_3$-dispersed Cr alloys for metallic interconnector of SOFC have been investigated as a fuction of $LaCrO_3$ content in the range of 5 to 25 vol.%. The Cr alloy were prepared by mixing Cr and $LaCrO_3$ powders in high-energy ball mill for 48h and by sintering under Ar atmosphere with 5vol.% $H_2$ for 10h at $1500^{\circ}C$. The alloys had a relative density of 95% and above. The Cr alloys in composed of two kind of small $LaCrO_3$ and large Cr particles. As the $LaCrO_3$ content increased, the Cr particle size decreased but the $LaCrO_3$ particle size remained contant. Also the oxidation tests show that the $LaCrO_3$-dispersed Cr is very resistant to oxidation in air. These results means that $LaCrO_3$-dispersed Cr is a useful material for metallic interconnect of planar SOFC.

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비오옴 ZnO 세라믹스의 형성과정에서 스피넬의 영향 (Effects of Spinel on the Formation Process of Nonohmic ZnO Ceramics)

  • 김경남;한상목
    • 한국세라믹학회지
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    • 제29권2호
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    • pp.101-106
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    • 1992
  • Sintering behavior, distribution of dopant oxides and electrical properties in the ZnO-Bi2O3-CoO-Sb2O3 and ZnO-Bi2O3-CoO-Sb2O3-Cr2O3 systems were studied. The linear shrinkage of ZnO varistors from 850 to 950$^{\circ}C$ was related to the decomposition reaction (py\longrightarrowsp+Bi2O3) of the pyrochlore phase. In the distribution of the dopant oxides (CoO, Sb2O3, Cr2O3), Co distribute uniformly throughout the sample, the distribution of Sb coincided with small particles (spinel phase, Zn7Sb2O12), and Cr distributed very consistently with Sb. The increase in breakdown voltage, due to the addition of Cr2O3, was not only attributed to the decrease in the ZnO grain size but also to the solution of Cr2O3 in the spinel phase. The leakage current (80% V60 ${\mu}\textrm{A}$) was increased by the addition of Cr2O3.

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NiCrAlY/ZrO$_2$-Y$_2$O$_3$ 복합코팅의 산화에 따른 조직관찰 (Microstructural Changes of NiCrAlY/ZrO$_2$-Y$_2$O$_3$ Composite Coatings By Oxidation)

  • 박기범;박진오;이동복
    • 한국표면공학회지
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    • 제35권2호
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    • pp.101-106
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    • 2002
  • The microstructural changes of $NiCrAlY/ZrO_2$-$Y_2$$O_3$ composite coatings that were manufactured by air-plasma-spraying were investigated using XRD and SEM/EDS. The as-sprayed microstructure consisted of (Ni,Cr)-rich regions, ($ZrO_2$-$Y_2$$O_3$)-rich regions, and $Al_2$$O_3$-rich layers that were formed during spraying owing to the oxidation of Al in NiCrAlY. During oxidation between 900 and $1100^{\circ}C$ in air, Cr in the (Ni,Cr)-rich regions diffused toward the $Al_2$$O_3$-rich layers, and oxidized to be dissolved in $A1_2$$O_3$-rich layers. The oxidation of Ni in the (Ni,Cr)-rich regions was less distinct, except at the outer surface of the coating.

산소가 첨가된 Cr 박막의 NH3 분위기에서의 질화 처리에 의한 구조적 특성 (Structural Characteristics by Nitridation of Oxygen Added Cr Thin Films in NH3 Atmosphere)

  • 김단비;김선태
    • 한국재료학회지
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    • 제31권11호
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    • pp.635-641
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    • 2021
  • Cr thin films with O added are deposited on sapphire substrate by DC sputtering and are nitrided in NH3 atmosphere between 300 and 900 ℃ for various times. X-ray diffraction results show that nitridation begins at 500 ℃, forming CrN and Cr2N. Cr oxides of Cr2O3 are formed at 600 ℃. And, at temperatures higher than 900 ℃, the intermediate materials of Cr2N and Cr2O3 disappear and CrN is dominant. The atomic concentration ratios of Cr and O are 77% and 23%, respectively, over the entire thickness of as-deposited Cr thin film. In the sample nitrided at 600 ℃, a CrN layer in which O is substituted with N is formed from the surface to 90 nm, and the concentrations of Cr and N in the layer are 60% and 40%, respectively. For this reason, CrN and Cr2N are distributed in the CrN region, where O is substituted with N by nitridation, and Cr oxynitrides are formed in the region below this. The nitridation process is controlled by inter-diffusion of O and N and the parabolic growth law, with activation energy of 0.69 eV.

Zn-Pr-Co-Er-M(M=Ni, Mg, Cr)산화물계 바리스터의 전기적, 유전적 특성 (Electrical and Dielectric Characteristics of Zn-Pr-Co-Er-M(M=Ni, Mg, Cr) Oxides-Based Varistors)

  • 남춘우;김명준
    • 한국세라믹학회지
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    • 제41권8호
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    • pp.605-609
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    • 2004
  • 다양한 금속산화물(NiO, MgO, Cr$_2$O$_3$) 첨가에 따른 ZnO 바리스터의 미세구조, 전기적, 유전적 특성을 조사하였다. 평균 결정립 크기는 NiO 첨가로 증가한 반면 Cr$_2$O$_3$ 첨가로 감소하였다 이로 인해 바리스터 전압은Cr$_2$O$_3$ 첨가시 더 높게 나타났다. 바리스터 가운데서 Cr$_2$O$_3$가 첨가된 바리스터가 비직선 지수가 40.5, 누설전류가 2.7 $\mu$A로 가장 우수한 비직선성을 나타내었으며, 유전손실도 0.0589로 비교적 낮게 나타났다.

석탄 가스화기에서의 크로미아 내화물 분석을 통한 화학적 침식 기구 규명 (Investigation of Corrosion Mechanism by Analyses of Spent Chromia Refractory fvom a Coal Gasifier)

  • 김한봄;오명숙
    • 에너지공학
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    • 제13권4호
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    • pp.281-290
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    • 2004
  • 석탄 가스화기에서 1000시간 이상 사용된 Cr$_2$O$_3$-Al$_2$O$_3$-ZrO$_2$ 내화물의 결정구조, 화학성분, 미세구조를 분석하여 석탄 슬래그에 의한 화학적 침식 메카니즘을 규명하였다 크로미아 내화물의 침식은 슬래그의 FeO와 $Al_2$O$_3$이 Cr$_2$O$_3$과 반응하며 일어나는 것으로 추정된다. 1차적으로 내화물의 슬래그 접촉면에서 슬래그의 FeO와 Cr$_2$O$_3$가 반응하여 FeCr$_2$O$_4$를 형성한다. 슬래그의 FeO가 모두 소모된 후 슬래그의 $Al_2$O$_3$이 Cr$_2$O$_3$ 입자와 반응하여 (Al, Cr)$_2$O$_3$를 형성하고, (Al, Cr)$_2$O$_3$상은 가장자리로부터 깨어져 미세한 입자를 형성한다. Cr$_2$O$_3$의 침식정도는 입자 크기와 치밀도에 따라 달라지며, 입자가 클수록, 치밀도가 높을수록 내침성이 증가하였다. ZrO$_2$는 화학적 성분의 변화 없었으나 슬래그 접촉면 부근에서 상 경계의 굴곡이 심해지거나 입자가 절단되는 물리적 침식의 영향을 받는다. 슬래그의 침투도는 일반적으로 석탄 주입구에서 아래로 내려갈수록 증가하나 슬래그 tap에서는 감소하였다.

M\ulcorner를 첨가한 Cr2O3의 전기전도도 (Electrical Conductivity of MgO-doped Cr2O3)

  • 박진성;김호기
    • 한국세라믹학회지
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    • 제24권2호
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    • pp.179-185
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    • 1987
  • The microstructure and the electrical conductivity of MgO-doped Cr2O3 were investigated as a function of oxygen partial presure, temperature, and MgO content. The grain size was estimated about 1.0$\mu\textrm{m}$. The solubility limit is increased with oxygen partial pressure. Above the solubility limit of MgO in Cr2O3, the spinel phase(MgCr2O4) is formed by the reaction of MgO and Cr2O3. The electrical conductivity of MgO-doped Cr2O3 within the solubility limit is increased with MgO content. Above the solubility limit, however, it is decreased with increasing MgO content because of the formation of the spinel phase.

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