• 한국세라믹학회지
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• 제52권6호
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• pp.417-422
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• 2015

In this study, we investigate the effect of porous $Al_2O_3$ substrate on the strengths of asymmetric structures after we prepare such a structure consisting of a dense $Li_2ZrO_3$ top layer and porous $Al_2O_3$ substrate layer. The porosity and elastic modulus of the substrate layer are controlled by sintering temperature, which has three values of 1150, 1250 and $1350^{\circ}C$. The porosity is controlled in the range of ~ 30-50 vol%, elastic modulus is ~80-120 GPa and elastic mismatch $E_s/E_c$ is ~ 0.6-1.0. Indentation stress-strain curves are obtained and analyzed to evaluate the yield stress of the asymmetric structure by concentrated local loading of WC balls. Conventional flexural strengths are also obtained to evaluate the strength of the asymmetric structure. The results indicate that the local yield strength of the asymmetric structure has mid-values between the top and the substrate layer; however, the flexural strength of the asymmetric structure are mainly influenced by elastic modulus and strength of the substrate.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2007년도 하계학술대회 논문집 Vol.8
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• pp.253-253
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• 2007

압전 액츄에이터 및 초음파진동자의 응용범위가 넒어짐에 따라 변위량, 응력 등을 개선시키기 위해 전기기계결합계수 kp 및 압전 d상수가 종전보다 큰 재료가 요구되고 있으며, 초음파진동자나 압전 모터와 같이 마찰에 의한 열손실이 많이 발생하는 액츄에이터에 적용할 큰 기계적품질계수롤 가지는 저손실 압전 액츄에이터 및 초음파진동자용 재료가 필요한 실정이다. PZT계 세라믹스는 높은 유전상수와 압전특성으로 전자세라믹스분야에서 가장 널리 사용되어지고 있지만, $1200^{\circ}C$이상의 높은 소결온도 때문에 $1000^{\circ}C$ 부근에서 급격히 휘발되는 PbO로 인한 환경오염과 기본조성의 변화로 인한 압전특성의 저하가 문제시 되고 있다. $Pb(Ni_{1/3}Nb_{2/3})O_3$는 약 $-120^{\circ}C$정도의 큐리온도룰 가지는 강유전체로 Pb(Zr, Ti)$O_3$계 세라믹스에 치환 시 유전상수와 전기기계결합계수를 개선시키는 대표적인 성분이다. 따라서 본 연구에서는 저온소결 저손실의 적층형 압전 액츄에이터를 개발하기 위해 PMS-PMN-PZT계 세라믹스에 $Pb(Ni_{1/3}Nb_{2/3})O_3$ 세라믹스를 치환하고 $Li_2CO_3$와 $Na_2CO_3$ ZnO를 소결조재로 사용하여 저온소결 하였으며 PNN 치환량에 따른 결과를 관찰 하였다.

• 분석과학
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• 제13권3호
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• pp.309-314
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• 2000

리튬 용융염($LiC+Li_2O$) 내에 미량으로 존재하는 핵분열생성물을 유도결합 플라스마 원자방출분광기(ICP-AES)를 이용하여 분석하였다. 분석대상 원소 중 감도가 가장 좋은 파장을 선택해 이들 파장에서 리튬 500, 1,000, 2,000 mg/L에 따른 분광학적 간섭 여부를 확인한 결과, 분석원소중 0.1 mg/L 이하의 Y, Nd, Sr, La, Eu의 방출세기는 리튬의 농도가 2,000 mg/L까지 증가시켜도 분광학적 간섭을 받지 않은 반면, Mo, Ba, Ru, Pd, Rh, Zr, Ce는 10% 에서 50% 이상 분광학적 간섭과 매트릭스에 의한 스펙트럼 방해가 나타났다. 리튬 매질로부터 미량 금속원소들을 군분리하기 위하여 모의 용융염 용액을 조제해 암모니아수를 가한 후 분리하고 다시 산처리하여 얻은 용액을 ICP-AES로 회수율을 측정하였다. 분석원소 중 Ru, Y, Rh, Zr, Nd, Ce, La, Eu의 회수율은 90% 이상인 반면 Mo, Ba, Pd, Sr는 낮은 회수율을 보여주었으며, 가해준 암모니아수 양이 증가할수록 회수율이 증가하는 경향을 보였다.

• 전기화학회지
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• 제21권4호
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• pp.80-87
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• 2018

웨어러블 디바이스, 전기자동차와 에너지저장시스템에 대한 전력 수요가 증가함에 따라 리튬이온 전지에 있어서 안전성은 가장 중요한 요소가 되었다. 이러한 문제를 해결하기 위해 가연성의 유기 액체전해질이 불연성의 고체전해질로 대체된 전고체 전지를 제조하려는 연구들이 진행되고 있다. 그러나 고체전해질은 자체 이온전도도가 상대적으로 낮고 전극/전해질 계면에서 높은 저항이 발생하므로 실질적인 활용에 제약이 있었다. 이에 유무기 소재로 구성된 복합전해질은 고체전해질의 단점을 극복할 수 있는 대안으로 떠오르고 있다. 본 연구에서는 PEO 전해질과 LLZO 고체전해질을 복합화하여 전해질을 제조하였고, LLZO 고체전해질 함량에 따라 결정성, 형상 및 전기화학 성능 분석을 진행하였다. 결과로부터 PEO 전해질 내에 LLZO 고체전해질의 최적 함량 및 균일한 분포가 전체 복합전해질의 이온전도도 향상에 중요한 요소임을 확인하였다.

• 전기화학회지
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• 제25권3호
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• pp.105-112
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• 2022

전고체전지의 상용화를 위해서는 상온에서 작동이 가능한 고체전해질 개발이 필수적이며 이온전도도가 높은 물질을 채택하여 전고체전지를 제조해야 한다. 따라서, 기존의 옥사이드 계열의 고체의 이온전도도를 높이기 위하여 이종원소가 도핑된 Li₇La₃Zr₂O₁₂ (LLZO)를 필러소재(Al, Nb-LLZO)로 사용하였으며, 상온에서 작동이 가능하도록 Poly(ethylene oxide)/Poly(propylene carbonate) (PEO/PPC) 기반의 가넷형 무기계 고체고분자 전해질을 제조하였다. 이원금속 원소를 도핑한 가넷형 무기계 필러와 PEO/PPC (1:1 비율로 섞인) 고분자를 1:2.4의 비율로 균일하게 교반하여 전해질을 합성해 상온과 60 ℃에서 전고체 전지의 전기학적 성능을 분석하였다. 제조한 복합 전해질은 이원금속의 도핑으로 인하여 이온전도도가 향상되었으며, PEO 단독으로 사용하는 전해질보다 PPC를 1:1로 첨가하였을 때 이온전도도 향상을 도와 60 ℃ 뿐만 아니라 상온에서 전고체 전지의 용량과 용량 유지율이 개선되었음을 확인하였다.

• 한국재료학회지
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• 제24권12호
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• pp.677-681
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• 2014

To increase the mechanical property of zirconia, we have investigated the phase change and the resulting hardness of zirconia ceramics by hydroxyapatite (HA) powder bed sintering. It was observed using X-ray diffraction that the cubic zirconia phase, which has a higher hardness value than that of the tetragonal phase, was obtained at the surface of 3 mol% $Y_2O_3$ doped tetragonal zirconia polycrystal (3Y-TZP) ceramics during the sintering process; in our experimental conditions, the phase change at the surface increased as the sintering time increased. We believe that the observed crystalline phase change originated from the decomposition of HA and the diffusion of CaO, as follows. CaO, which was derived from the decomposition of HA at high temperature ($1400^{\circ}C$), diffused into the surface of 3Y-TZP and acted as a stabilizer. As a result, the Vickers hardness value of the treated specimens was higher than that of the non-treated specimen due to the formation of the cubic phase on the surface of 3Y-TZP.

• 대한방사성의약품학회지
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• 제3권2호
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• pp.103-112
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• 2017

The combination of nanoparticle with radioisotope could give the in vivo information with high sensitivity and specificity. However, radioisotope labeling of nanoparticle is very difficult and radioisotopes have different physicochemical properties, so the radioisotope selection of nanoparticle should be carefully considered. $^{18}F$ was first option to be considered for labeling of nanoparticle. For the labeling of $^{18}F$ with nanoparticle, Prosthetic group is widely used. Iodine, another radioactive halogen, is often used. Since radioiodine isotopes are various, they can be used for different imaging technique or therapy in the same labeling procedures. $^{99m}Tc$ can easily be obtained as pertechnatate ($^{99m}{TcO_4}^-$) by commercial generator. Ionic $^{68}Ga$ (III) in dilute HCl solution is also obtained by generator system, but $^{68}Ga$ can be substituted for $^{67}Ga$ because of the short half-life (67.8 min). $^{64}Cu$ emits not only positron but also ${\beta}-particle$. Therefore $^{64}Cu$ can be used for imaging and therapy at the same time. These radioactive metals can be labeled with nanoparticle using the bifunctional chelator. $^{89}Zr$ has longer half-life (78.4 h) and is used for the longer imaging time. Unlike different metals, $^{89}Zr$ should use the other chelate such as DFO, 3,4,3-(LI-1,2-HOPO) or DFOB.

• 한국광물학회지
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• 제13권3호
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• pp.147-163
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• 2000

The mineralogy and chemical composition of reddish to brownish yellow residual soils, so called "Hwangto" have been examined according to representative host rocks. The result of the study indicates that Hwangto consists of 40-80% clay minerals and various minerals such as quartz, feldspar, hornblende, goethite, and gibbsite. Clay minerals include kaolinite, halloysite, illite, hydroxy interlayered vermiculite (HIV), mica/vermiculite interstratifield mineral and chlorite. The mineralogical constituents and contents of Hwangto were different depending on the types of host rocks. Moreover, the Jurassic granitic rocks contain relatively more kaolin minerals, whereas the Cretaceous granitic rocks contain more HIV and illite. In addition, reddish Hwangto contains relatively more kaolinite and HIV, and yellowish Hwangto contains more illite and halloysite. It is suggested that feldspars and micas of host rocks were chemically weathered into illite, halloysite, illite/vermiculite interstratified minerals, and HIV, and finally into kaolinite. Compared with their host rocks, the major chemical compositions of Hwangto tend to contain more $Al_2O_3,\;Fe_2O_3,\;H_2O$ in amount and less Ca, Mg, and Na. Hwangto contains relatively high amount of trace elements, P, S, Zr, Sr, Ba, Rb, and Ce including considerable amount of Li, V, Cr, Zn, Co, Ni, Cu, Y, Nb, La, Nd, Pb, Th in excess of 10 ppm. Relatively high amount of most trace elements were detected in the Hwangto. The major and minor chemical compositions of the Hwangto were different depending on the types of host rocks. However, their difference was in the similar range compared with the compositions of host rocks.

• Journal of Mechanical Science and Technology
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• 제20권1호
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• pp.1-12
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• 2006

This work reviews the effects of catalyst formulation and exhaust gas composition on soot oxidation in CDPF (Catalytic Diesel Particulate Filter). DOC's (Diesel Oxidation Catalysts) have been loaded with Pt catalyst (Pt/$Al_{2}O_3$) for reduction of HC and CO. Recent CDPF's are coated with the Pt catalyst as well as additives like Mo, V, Ce, Co, Fe, La, Au, or Zr for the promotion of soot oxidation. Alkali (K, Na, Cs, Li) doping of metal catalyst tends to increase the activity of the catalysts in soot combustion. Effects of coexistence components are very important in the catalytic reaction of the soot. The soot oxidation rate of a few catalysts are improved by water vapor and NOx in the ambient. There are only a few reports available on the mechanism of the PM (particulate matter) oxidation on the catalysts. The mechanism of PM oxidation in the catalytic systems that meet new emission regulations of diesel engines has yet to be investigated. Future research will focus on catalysts that can not only oxidize PM at low temperature, but also reduce NOx, continuously self-cleaning diesel particulate filters, and selective catalysts for NOx reduction.

• 한국방사성폐기물학회:학술대회논문집
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• 한국방사성폐기물학회 2004년도 Proceedings of the 4th Korea-China Joint Workshop on Nuclear Waste Management
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• pp.73-82
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• 2004

This paper studies the leaching behaviors of pyrochlore-rich synroc incorporated 46.8wt% simulated actinides waste under the five simulated geological disposal media, which included the bentonite, granite, granite ＋ ferroferric oxide, granite ＋ cement, bentonite ＋ ferroferric oxide, respectively. The mass loss rates reached to equilibrium after 182 day and was 10-7 g/$\textrm{mm}^2{\cdot}d$. That suggests the mass loss rate of pyrochlore-rich synroc, loaded 46.8wt% actinides waste, was very low. The surfaces of the leached specimens were analyzed by XRD, SEM/EDS. The experimental results show that the pyrochlore-rich synroc samples in the systems, which contained bentonite and cement, have two new phases formed on the leached specimens surface at $90^{\circ}C$ for 728d; The bentonite and cement can retard the elements leaching; $Fe_3O_4$ can speed the elements leaching; Expect for Ti ion depleted on the sample surface, other ion, such as U, Zr, AI, Ca, were in equable states and Ba ion was enriched during test time, which indicated the simulated disposal media have good ability to retard the leaching behavior of the pyrochlore-rich synroc.