• 제목/요약/키워드: $Ni^{2+}$

검색결과 6,591건 처리시간 0.038초

Ni-NiAl 확산대에서 $Ni_3Al$ 상의 형성과 반응확산 (Reaction diffusion and formation of$Ni_3Al$ phase at the Ni-NiAl diffusion couple)

  • 정승부
    • Journal of Welding and Joining
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    • 제15권3호
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    • pp.128-135
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    • 1997
  • Reaction diffusion and formation of $Ni_3Al$phase with $L1_2$ structure have been studied in temperature range of 1432K to 1573K using the diffusion couple of (Ni-40, 5at%Al)/(Ni-14, 1at%Al) and (Ni-49, 2at%Al)/ (Nickel). The layer growth of Ni$_{3}$Al pyhase in the annealed diffusion couple was measured by optical microscope and electron probe microanalyzer (EPMA). The layer growth of $Ni_3Al$phase in diffusion zone obeyed the parabolic law without any indication of grain boundary effects. The layer growth of $Ni_3Al$phase in temperature range of 1423K to 1573K was mainly controlled by the volume diffusion mechanism. The rate of layer growth of $Ni_3Al$phase was found to be colsely related to the composition of intermetallic compound NiAl phase. The activation energy for layer growth of $Ni_3Al$phase was calculated to be 127kJ/mol.

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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.

Investigation of Al modification as cationic dopants in Nirich LiNi0.91Co0.06Mn0.03O2 cathode

  • Ye-Wan Yoo;Seung-Hwan Lee
    • Journal of Ceramic Processing Research
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    • 제23권5호
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    • pp.566-569
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    • 2022
  • In this paper, we have successfully prepared Al-doped Ni-rich LiNi0.91Co0.06Mn0.03O2 cathodes. The structural properties andelectrochemical performances are studied according to Al cationic doping. It can be confirmed that the crystallinity and cationdisordering of Ni-rich LiNi0.91Co0.06Mn0.03O2 were improved by Al doping. Based on such excellent structural quality, theelectrochemical performance of Al doping LiNi0.91Co0.06Mn0.03O2 was superior to that of pristine LiNi0.91Co0.06Mn0.03O2. The Aldoping Ni-rich NCM has an initial discharge capacity of 209.2 mAh g-1. In addition, it shows superior rate capability byshowing capacity retention of 58.5% under a high rate of 6.0 C. Therefore, it can be judged that Al doping LiNi0.91Co0.06Mn0.03O2can be applied to next-generation cathode for long-distance and fast-charging electric vehicles.

ZnO-$SnO_2$계 Spinel 채료에 대한 NiO, $TiO_2$의 영향 (Influence of NiO, $TiO_2$ on ZnO-$SnO_2$ System Spinel Pigment)

  • 이응상;황성윤
    • 한국세라믹학회지
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    • 제14권3호
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    • pp.187-192
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    • 1977
  • For the purpose researching to the influence of tetrahedral and octahedral preference of cations of $Ni^{2+}$, $Ti^{4+}$ upon the formation and the color development of the $ZnO-SnO_2$ spinel containing $Ni^{2+}$ and $Ti^{4+}$ ions, the gradual substitution of $Ni^{2+}$ ions for $Zn^{2+}$ ions and of $Ti^{4+}$ ions for $Sn^{4+}$ ions of the spinel in NiO-ZnO-$SnO_2$-$TiO_2$ system was carried out. On samples prepared by calcining the oxide and basic cabonate mixtures at $1300^{\circ}C$ for 2 hours, the X-ray analysis, measurement of reflectance and the test of their stabilaity as a glaze pigment were also carried out. The results are summarized as follows 1) Single spinel was formed completely to x=1 in the $xNiO\cdot(2-x)ZnO\cdot{SnO}_2$system, and gave brilliant lightgreen hue. Moreover, $NiO\cdot{ZnO}\cdot{SnO}_2$ formed easily spinel than $NiO\cdot{MgO}\cdot{SnO}_2$ because Zn^{2+}$ ions had more strong tetrahedral preference than $Mg^{2+}$ ions. 2) As the gradual substitution of $Ti^{4+}$ ions for $Sn^{4+}$ ions in $NiO\cdot{MgO}\cdot{SnO}_2$ system, the spinels formed well and was nearly not changed in the hue. 3) The results of glaze test. (1) As the gradual substitution of $Ni^{2+}$ ions for $Zn^{2+}$ ions, the color changed from dull white to graish broun gradually in calcium-zinc glaze and calcium glaze, and from white to beige in tile glaze. (2) As the gradual substitution of $Ti^{4+}$ ions for $Sn^{4+}$ ions in $NiO-ZnO-SnO_2-TiO_2$ system, the color was become dull generally and was not change in tile glaze.

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Exchange Coupling in NiFe/Ni Bilayer Fabricated By Electrodeposition

  • Kim, D.Y.;Jeon, S.J.;Kim, K.W.;Yoon, S.S.
    • Journal of Magnetics
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    • 제16권2호
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    • pp.97-100
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    • 2011
  • Bilayers of soft NiFe (150 nm-420 nm) on hard Ni (150 nm) were prepared by electrodeposition. The process of magnetization reversal in the NiFe/Ni bilayers was then investigated. The hysteresis loop generated by a magnetization reversal of soft NiFe under a positive saturation state of a hard Ni layer shows a shift along the negative field axis, which is clear evidence for the exchange spring effect in the NiFe/Ni bilayers. The dependence of the coercive field $H_c$ and exchange bias field Hex on the thickness of the NiFe layer was also investigated. As the NiFe thickness increases from 150 nm to 420 nm, both $H_c$ and $H_{ex}$ decrease rapidly from $H_c$= 51.7 Oe and $H_{ex}$ = 12.2 Oe, and saturate to $H_c$ = 5.8 Oe and $H_{ex}$ = 3.5 Oe.

제조 공정 Parameter에 따른 NiCuZn Ferrite의 투자율과 $Q_{max}$ 주파수 변화 (The Variation of Permeability and$Q_{max}$ Frequency with Processing Parameters in NiCuZn Ferrites)

  • 신재영;박지호;박진채;한종수;송병무
    • 한국자기학회지
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    • 제7권1호
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    • pp.19-24
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    • 1997
  • 적층형 chip inductor 소재인 NiCuZn ferrite의 제조 공정 조건 및 조성을 선정하였다. NiCuZn ferrite의 NiO 함량이 증가할 수록 저온 소결에 필요한 Fe$_{2}$O$_{3}$ 결핍량은 점차 증가하였고, NiO 함량과 Co$_{3}$O$_{4}$ 첨가량을 변화하여 투자율을 12 ~ 562 범위에서 제어할 수 있었다. NiCuZn ferrite의 투자율이 562에서 60으로 변화함에 따라서 Q$_{max}$ 주파수는 3 MHz에서 50 MHz 범위로 제어할 수 있었다. 이때 Q$_{max}$ 주파수(Y)와 투자율(X)은 log Y = 4.2-1.4 log X의 상관관계를 나타내었다.

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기계적인 합금에 의한 Mg-10wt.%Ni 수소저장합금의 개발 (Development of Mg-10wt.%Ni Hydrogen-Storage Alloy by Mechanical Alloying)

  • 송명엽
    • 한국수소및신에너지학회논문집
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    • 제9권4호
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    • pp.143-150
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    • 1998
  • 순수한 Mg의 수소와의 반응속도를 증가시키기 위하여 기계적으로 합금처리한 Mg-10wt.%Ni 혼합물의 수소화물 형성 분해 성질을 조사하였다. 수소화물 형성 분해 cycling을 시킴에 따라 $Mg_2Ni$상이 형성되고 그 양이 증가한다. 기계적인 합금 처리와 수소화물 형성 분해 cycling의 주요 효과는 결함의 수를 증가시키고, 비표면적을 크게하는 것으로 생각된다. 기계적으로 합금처리한 Mg-10wt.%Ni 혼합물은 활성화가 용이하게 이루어지고, 순수한 Mg, Mg-10wt.%Ni합금, Mg-25wt.%Ni합금, 그리고 $Mg_2Ni$합금과 비교하여, 수소화물 형성 속도와 수소 저장 용량이 아주 크고, 수소화물 분해 속도가 비교적 높다.

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일방향 응고한 Ni기 초내열 공정복합재료의 열적 안정성에 관한 연구 (A Study on the Thermal Stability of Unidirectionally Solidified Eutectic Composites of Ni-Base Superalloys)

  • 이현규;공창덕
    • 한국추진공학회지
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    • 제2권1호
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    • pp.67-77
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    • 1998
  • Ni/$Ni_3$Al-$Ni_3$Nb(${\gamma}$/${\gamma}$'-${\delta}$), Ni-$Ni_3$Nb(${\gamma}$-${\delta}$) 공정복합재료를 일방향 응고하였으며, 성장속도에 따른 경도변화, 고온에서 미세조직의 안정성을 층상간격의 영향에 대해 연구하였다. 초내열합금 공정복합재료의 층상간격은 ${\lambda}^2$R=상수라는 관계식에 의하여 성장속도(R)와 함께 변화하였다. 초내열합금 공정복합 재료를 위한 항온열처리의 결과는 이 연구에 이용되었다. 공정복합재료는 고온에서 미세구조의 안정성이 층상간격의 증가 때문에, 경도는 성장속도의 증가 때문에 향상되었다.

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The Electrochemical Behavior of Ni-base Metallic Glasses Containing Cr in H2SO4 Solutions

  • Arab, Sanaa.T.;Emran, Khadijah.M.;Al-Turaif, Hamad A.
    • 대한화학회지
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    • 제56권4호
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    • pp.448-458
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    • 2012
  • In order to develop alloy resistance in aggressive sulphat ion, the corrosion behavior of metallic glasses $Ni_{92{\cdot}3}Si_{4.5}B_{32}$, $Ni_{82,3}Cr_7Fe_3Si_{4.5}B_{3.2}$ and $Ni_{75.5}Cr_{13}Fe_{4.2}Si_{4.5}B_{2.8}$ (at %) at different concentrations of $H_2SO_4$ solutions was examined by electrochemical methods and Scanning Electron Microscope (SEM) and X-ray Photoelectron Microscopy (XPS) analyses. The corrosion kinetics and passivation behavior was studied. A direct proportion was observed between the corrosion rate and acid concentration in the case of $Ni_{92{\cdot}3}Si_{4.5}B_{32}$ and $Ni_{75.5}Cr_{13}Fe_{4.2}Si_{4.5}B_{2.8}$ alloys. Critical concentration was observed in the case of $Ni_{82,3}Cr_7Fe_3Si_{4.5}B_{3.2}$ alloy. The influence of the alloying element is reflected in the increasing resistance of the protective film. XPS analysis confirms that the protection film on the $Ni_{92{\cdot}3}Si_{4.5}B_{32}$ alloy was NiS which is less protective than that formed on Cr containing alloys. The corrosion rate of $Ni_{82,3}Cr_7Fe_3Si_{4.5}B_{3.2}$ and $Ni_{75.5}Cr_{13}Fe_{4.2}Si_{4.5}B_{2.8}$. alloys containing 7% and 13% Cr are $7.90-26.1{\times}10^{-3}$ mm/y which is lower about 43-54 times of the alloy $Ni_{92{\cdot}3}Si_{4.5}B_{32}$ (free of Cr). The high resistance of $Ni_{75.5}Cr_{13}Fe_{4.2}Si_{4.5}B_{2.8}$ alloy at the very aggressive media may due to thicker passive film of $Cr_2O_3$ which hydrated to hydrated chromium oxyhydroxide.

고온용융염계 산화분위기에서 초합금의 부식거동 (Corrosion Behavior of Superalloys in Hot Molten Salt under Oxidation Atmosphere)

  • 조수행;임종호;정준호;이원경;오승철;박성원
    • 한국방사성폐기물학회:학술대회논문집
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    • 한국방사성폐기물학회 2004년도 학술논문집
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    • pp.285-291
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    • 2004
  • LiCl-$Li_2O-O_2$ 용융염계에서 용융염 취급장치의 구조재료를 위한 평가의 일환으로 Inconel 718, X-750, Haynes 75, 263 합금의 부식거동을 분위기온도; $650^{\circ}C$, 부식시간: 24~168h, $Li_2O$농도; 3wt%, 혼합가스농도; Ar-10%$O_2$에서 조사하였다. LiCl-$Li_2O-O_2$ 용융염계에서 부식속도는 Haynes 263 < Haynes 75 < Inconel X-750 < Inconel 718 순서로 나타났으며, Haynes 263 합금이 가장 우수한 내부식성을 나타내었다. Haynes 75의 부식생성물은 $Cr_2O_4$, $NiFe_2O_4$, $LiNiO_2$, $Li_2NiFe_2O_4$, Inconel 718의 부식생성물은 $Cr_2O_4$$NiFe_2O_4$ 이며 Haynes 263은 $Li(Ni,Co)O_2$, $NiCr_2O_4$$LiTiO_2$, Inconel X-750은 $Cr_2O_3$, $NiFe_2O_4$,$FeNi_3$, (Al,Nb,Ti)$O_2$의 부식생성물을 나타내었다. Haynes 263은 국부부식의 거동을 보이는 반면, Haynes 75, Inconel 718 및 Inconel X-750은 전면 부식 거동을 나타내었다.

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