• 한국자기학회지
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• 제15권2호
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• pp.85-91
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• 2005

Effect of different cations to the formation of iron oxyhydroxide was studied using $M\ddot{o}ssbauer$ spectroscopy, X-ray diffraction (XRD) and BET. Redox Potential and pH were measured for the determination of the internal reaction rate, as well. The phases of iron oxyhydroxide could not be the same with each other, due to the presence of different cations in solution. Although the oxyhydroxide compound was composed of the same phases, the fraction of each phase was different from each other. The internal reaction rate was varied by the substitution of cation. It could be a cause of the different phase and particle size of oxyhydroxide compound.

• Journal of Magnetics
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• 제14권2호
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• pp.93-96
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• 2009

The Mn-substituted M-type Ba-ferrite ($BaFe_{12-x}Mn_xO_{19}$; x = 0, 2, 4, 6) powders were prepared by the HTTD (High Temperature Thermal Decomposition) method. The effect of $Mn^{3+}$ Jahn-Teller ions on the magnetic properties has been studied by x-ray diffraction, vibrating sample magnetometry, and $M{\ddot{o}}ssbauer$ spectroscopy. With increasing Mn substitution, the lattice parameter $a_0$ increases while $c_0$ decreases. The magnetocrystalline anisotropy constants ($K_1$) were determined as 2.9, 2.2, 1.8, and, $1.3{\times}10^6\;erg/cm^3$ for x = 0, 2, 4, and 6, respectively, by the LAS method. We have studied the change of cation distribution by $M{\ddot{o}}ssbauer$ spectroscopy which is closely related to $K_1$.

• 한국재료학회지
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• 제12권10호
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• pp.796-802
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• 2002

Effect of nine different cations to the formation of iron oxyhydroxide was studied using Mossbauer spectroscopy, XRD and BET. The Redox Potential and pH were measured for the determination of the internal reaction rate, as well. The phases of iron oxyhydroxide could not be the same with each other, due to the present of different cations in solution. Although the oxyhydroxide compound were composed of the same phases, the fraction of each phase was different from each other. The internal reaction rate was varied by the substitution of cation. It could be a cause of the different phase and particle size of oxyhydroxide compound.

• 자원환경지질
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• 제21권2호
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• pp.175-184
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• 1988

감포지역(甘浦地域)의 용동리에서 용동리응회암(龍洞里凝灰岩)내에 배태되는 Ca-몬모릴로나이트들은 비록 동일층준(同一層準)에서 산출(産出)되나 제한적(制限的)이지만 화학조성(化學組成)의 차이(差異)가 나타난다. 이들의 열적특성은 "비정상형(型)"으로 나타나며, 탈수와 관계된 흡열반응피크의 온도(溫度)는 사면체내의 Si를 치환한 Al의 양적비에 따라 약간변화된다. 이러한 사실은 제한적인 화학조성의 변화는 열적특성에 큰 영향을 미치지 못함을 지시한다. 시차주사열량 측정결과 2가의 양이온으로 치환 된 시료의 경우 1가의 양이온으로 치환된 시료보다 흡열용량이 증가되는 경향을 보이므로 시료내의 우세한 양이온의 종류를 예상할 수 있으며, 전기음성도가 큰 이온일수록 더 많은 물분자를 취(取)함을 알수있다.

• Nuclear Engineering and Technology
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• 제9권2호
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• pp.75-81
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• 1977

원자력 발전소에서 나오는 방사성 핵종이 clay 속에 고정되는 반응기구를 분석하기 위해서 clay의 양이온 교환능을 Sawhney 방법으로 측정했다. Clinoptilolite, vermiculite 및 sodalite들의 PH dependent CEC를 측정한 결과 총 양이온 교환능의 약 70% 정도가 영구 고정되어진다고 생각되는 neutral salt CEC에 의해 일어나고 나머지는 가역과정인 clay 속의 유기물질과 다른 급속(Al, Mg)의 치환에 의해서 일어난다는 결론을 얻었으며, pH 9 이상에서 clay에 의한 방사성 핵종의 제거는 이온 교환 기구에 의한 고정보다 오히려 중금속 이온의 침전에 의해서 더 많이 일어난다는 것도 밝혀냈다. 그리고 연속 치환에 의해서 처리된 Na-clay는 방사성 핵종제거에 상당히 향상된 제거 효율을 나타내고 있다.

• The Korean Journal of Ceramics
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• 제5권1호
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• pp.40-43
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• 1999

In order to investigate Sn substitution sites and interstitial O atoms in tin-doped indium oxide, molecular dynamics (MD) simulations were carried out. There are two kinds of cation sites in $In_2O_3$, namely b-site and d-site. NTP-MD simulations under the condition of 300 K and 0 GPa were performed with two kinds of cells substituted by Sn atoms at each site. The excess oxygen atom accompanied with Sn doping was also taken into consideration. According to the calculations of Sn potential energies in each site, it was revealed that Sn atoms were substituted for b-sites rather than for d-sites. It was also revealed that the interstitial excess oxygen atoms tend to be connected with the Sn atoms substituted for the d-sites Sn rather than for the b-site. There MD simulation results well agreed with the experimental results.

• 한국결정성장학회지
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• 제9권2호
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• pp.245-250
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• 1999

본 연구에서는$(Li_{0.5}La_{0.5})_{1-y}Sr_yTi_{1-x}Mn_xO_3$와 같은 조성계를 택하여 고용범위 내에서 Sr과 Mn을 변화시켜가며 이온전도도를 고찰하였다. 결과 Sr 치환의 경우 y=0.05 이상에서는 전도도가 급격히 감소하였으며 이는 이온전도에 기여하는 리튬의 절대량이 감소하였기 때문인 것으로 판단된다. Mn의 경우 치환에 의한 격자상수의 변화 외에 Jahn-Teller distortion에 의하여 전도도가 영향을 받는다는 것을 알 수 있었다. A-site와 B-site의 이온이 독립적으로 이온전도에 기여한다는 것을 알 수 있었으며 x=0.0006, y=0.05에서 이온전도도는$2.8{\times}10^{-2}$ S/cm였다.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 1995년도 추계학술대회 논문집
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• pp.217-220
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• 1995

By substituting Cd$\^$2+/ into both A-site and B-site in PNN-PZ-PT ternary perovskite material, it is possible to determine the effects of the substitution site of Cd$\^$2+/ on sintering behavior. Sintering was performed in the temperature range from 1000$^{\circ}C$ to 1300$^{\circ}C$. The substitution site of Cd$\^$2+/ is identified by XPS spectra. Although Cd$\^$2+/ is substituted into both A-site and B-site in PNN-PZ-PT, Cd$\^$2+/ prefers A-site to B-site. The density is influenced by substitution site of Cd$\^$2+/. If Cd$\^$2+/ replaces Pv$\^$2+/, weight gain is observed during sinterig process. On the contrary, if Cd$\^$2+/ replaces Ni$\^$2+/, weight loss is promoted during sintering. From these weight changes, it is believed that Cd$\^$2+/ changes the bonding strength between B-site cation and oxygen of octahedron in perovskite structure. The changes of lattice parameters as a function of Cd$\^$2+/ content were consistent with those of the bonding strength. The densities of A-site-doped compositions were higher than those of B-site-doped composition.

• Journal of Magnetics
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• 제15권1호
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• pp.25-28
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• 2010

This study examined the crystallographic and magnetic properties of vanadium-substituted lithium cobalt titanium ferrite, $Li_{0.7}Co_{0.2}Ti_{0.2}V_{0.2}Fe_{1.7}O_4$. Ferrite was synthesized using a conventional ceramic method. The samples annealed below $1040^{\circ}C$ showed X-ray diffraction peaks for spinel and other phases. However, the sample annealed above $1040^{\circ}C$ showed a single spinel phase. The lattice constant of the sample was $8.351\;{\AA}$, which was relatively unaffected by vanadium-substitution. The average grain size after vanadium-substitution was $13.90\;{\mu}m$, as determined by scanning electron microscopy. The M$\ddot{o}$ssbauer spectrum could be fitted to two Zeeman sextets, which is the typical spinel ferrite spectra of $Fe^{3+}$ with A and B sites, and one doublet. From the absorption area ratio of the M$\ddot{o}$ssbauer spectrum, the cation distribution was found to be ($Co_{0.2}V_{0.2}Fe_{0.6})[Li_{0.7}Ti_{0.2}Fe_{1.1}]O_4$. Vibrating sample magnetometry revealed a saturation magnetization and coercivity of 36.9 emu/g and 88.6 Oe, respectively, which were decreased by vanadium-substitution.

• 한국자기학회:학술대회 개요집
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• 한국자기학회 2012년도 자성 및 자성재료 국제학술대회
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• pp.170-171
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• 2012