• 한국재료학회지
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• 제19권2호
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• pp.85-89
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• 2009

Nano-crystalline hydroxyapatite (HAp) films were formed at the Ti surface by a single-step microarc oxidation (MAO), and HAp-zirconia composite (HZC) films were obtained by subsequent chemical vapor deposition (CVD) of zirconia onto the HAp. Through the CVD process, zero- and one-dimensional zirconia nanostructures having tetragonal crystallinity (t-ZrO2) were uniformly distributed and well incorporated into the HAp crystal matrix to form nanoscale composites. In particular, (t-$ZrO_2$) was synthesized at a very low temperature. The HZC films did not show secondary phases such as tricalcium phosphate (TCP) and tetracalcium phosphate (TTCP) at relatively high temperatures. The most likely mechanism for the formation of the t-$ZrO_2$ and the pure HAp at the low processing temperature was proposed to be the diffusion of $Ca^{2+}$ ions. The HZC films showed increasing micro-Vickers hardness values with increases in the t-$ZrO_2$ content. The morphological features and phase compositions of the HZC films showed strong dependence on the time and temperature of the CVD process. Furthermore, they showed enhanced cell proliferation compared to the $TiO_2$ and HAp films most likely due to the surface structure change.

• 열처리공학회지
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• 제18권5호
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• pp.312-317
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• 2005

The precipitation process in Cu-0.2 wt.%Cr-0.05 wt.%Zr alloys has been studied by electrical electrical resistivity measurements. The kinetics of precipitation could be well described by Johnson-Mehl-Avrami equation, $f(t)=1-\exp(-kt^n)$. The values of n were found to be in the range of 0.36~0.42 at first stage and 1.3~1.6 at second stage. The activation energy was determined by cross-cut method and was 80~89 kJ/mol. The value is similar to the energy for the migration of either a vacancy or a vacancy-solute complex through the lattice.

• 한국세라믹학회지
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• 제49권1호
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• pp.84-89
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• 2012

Attempts were made to develop a stable gray pigment at reducing atmosphere, substituting Ti in $ZrTiO_4$ with Mn, Fe, Co and Cu The pigment synthesized at $1300~1500^{\circ}C$ by solid state method with the composition of $ZrTi_{1-x-y}A_xB_yO_4$ (x = y = 0.005, 0.015, 0.035, 0.055, 0.075, 0.095, 0.115, 0.135, 0.155, 0.175 and 0.195 mole, A = Mn(III), Fe(III), Co(II, III) and Cu(II) (chromophores), B = Sb (counterion). The pigments were fired at $1400^{\circ}C$ for 3 h with substitute amount changes of Mn, Fe, Co and Cu to $ZrTiO_4$ crystals, and analyzed by Raman spectroscopy to figure out substitute limits. Results indicated 0.035 mole for Mn, 0.115 mole for Fe, 0.015 mole for Co and 0.015 mole for Cu as substitute limits, respectively. Figs. 1, 2, 3, and 4 represent each substitute pigments of Mn, Fe, Co and Cu. Synthesized pigment was applied to a lime and a lime-magnesia glaze at 7 wt% each, and fired at reducing atmosphere of $1240^{\circ}C$, soaking time 1h. Gray color was obtained with CIE-$L^*a^*b^*$ values at 44.55, -0.65, 1.19(Mn), 40.36, -0.90, 0.30(Fe), 42.63, -0.03, -1.49(Cu) and -40.79, -0.28, -0.91(Co), respectively.

• 대한방사성의약품학회지
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• 제1권1호
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• pp.1-8
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• 2015

It is essential use of long term half life radioisotopes for positron emission tomography (PET) imaging study of biopharmaceuticals because most of biopharmaceuticals have long biological half-life. Some representative isotopes are $^{124}I$, $^{64}Cu$, $^{89}Zr$ and so on. These PET radioisotopes and their radiopharmaceuticals have recently received growing interest because of long half life and good imaging properties. Furthermore, $^{64}Cu$ and $^{89}Zr$ can be used in a number of radiopharmaceuticals due to its ease of conjugation to peptides and antibodies using the proper chelator. In recent years, since $^{124}I$ was first developed in 2005, we have been studied to develop an efficient method and procedure for producing these radioisotopes, and we have made considerable progress in production of long term half life radioisotopes. This review introduces the general production system, purification procedure, and several advances on targeting method for $^{124}I$ and $^{64}Cu$ in KIRAMS.

• 전기학회논문지
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• 제57권11호
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• pp.2015-2022
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• 2008

The effect of content of $Al_2O_3+Y_2O_3$ sintering additives on the densification behavior, mechanical and electrical properties of the pressureless-sintered $SiC-ZrB_2$ electroconductive ceramic composites was investigated. The $SiC-ZrB_2$ electroconductive ceramic composites were pressurless-sintered for 2 hours at 1,700[$^{\circ}C$] temperatures with an addition of $Al_2O_3+Y_2O_3$(6 : 4 mixture of $Al_2O_3$ and $Y_2O_3$) as a sintering aid in the range of $8\;{\sim}\;20$[wt%]. Phase analysis of $SiC-ZrB_2$ composites by XRD revealed mostly of $\alpha$-SiC(6H), $ZrB_2$ and In Situ YAG($Al_5Y_3O_{12}$). The relative density, flexural strength, Young's modulus and vicker's hardness showed the highest value of 89.02[%], 81.58[MPa], 31.44[GPa] and 1.34[GPa] for $SiC-ZrB_2$ composites added with 16[wt%] $Al_2O_3+Y_2O_3$ additives at room temperature respectively. Abnormal grain growth takes place during phase transformation from $\beta$-SiC into $\alpha$-SiC was correlated with In Situ YAG phase by reaction between $Al_2O_3$ and $Y_2O_3$ additive during sintering. The electrical resistivity showed the lowest value of $3.l4{\times}10^{-2}{\Omega}{\cdot}cm$ for $SiC-ZrB_2$ composite added with 16[wt%] $Al_2O_3+Y_2O_3$ additives at 700[$^{\circ}C$]. The electrical resistivity of the $SiC-TiB_2$ and $SiC-ZrB_2$ composite was all negative temperature coefficient resistance (NTCR) in the temperature ranges from room temperature to 700[$^{\circ}C$]. Compositional design and optimization of processing parameters are key factors for controlling and improving the properties of SiC-based electroconductive ceramic composites.

• The Journal of Advanced Prosthodontics
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• 제14권6호
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• pp.346-359
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• 2022

PURPOSE. Four and six implant-supported fixed full-arch prostheses with various framework materials were assessed under different loading conditions. MATERIALS AND METHODS. In the edentulous maxilla, the implants were positioned in a configuration of four to six implant modalities. CoCr, Ti, ZrO₂, and PEEK materials were used to produce the prosthetic structure. Using finite element stress analysis, the first molar was subjected to a 200 N axial and 45° oblique force. Stresses were measured on the bone, implants, abutment screw, abutment, and prosthetic screw. The Von Mises, maximum, and minimum principal stress values were calculated and compared. RESULTS. The maximum and minimum principal stresses in bone were determined as CoCr < ZrO₂ < Ti < PEEK. The Von Mises stresses on the implant, implant screw, abutment, and prosthetic screws were determined as CoCr < ZrO₂ < Ti < PEEK. The highest Von Mises stress was 9584.4 Mpa in PEEK material on the prosthetic screw under 4 implant-oblique loading. The highest maximum principal stress value in bone was found to be 120.89 Mpa, for PEEK in 4 implant-oblique loading. CONCLUSION. For four and six implant-supported structures, and depending on the loading condition, the system accumulated different stresses. The distribution of stress was reduced in materials with a high elastic modulus. When choosing materials for implant-supported fixed prostheses, it is essential to consider both the number of implants and the mechanical and physical attributes of the framework material.

• 한국수소및신에너지학회논문집
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• 제21권2호
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• pp.89-97
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• 2010

$Al_2O_3$, $TiO_2$, $ZrO_2$, $Al_2O_3-TiO_2$, $Al_2O_3-ZrO_2$, 및 $TiO_2-ZrO_2$ 혼합 산화물을 지지체로 한 Ni 기반 혼합 산화물을 졸-겔법으로 제조하였다. 제조된 혼합 산화물은 1173K에서 열처리 한 후 구조적 특성 변화를 전자현미경 및 X-선 회절 분석을 이용하여 관찰하였으며, 수소를 이용한 승온 환원(TPR; temperature-programmed reduction) 실험을 통하여 1173K 까지 각 시료들의 환원 피크를 비교 고찰하였다. $Al_2O_3$ 또는 $TiO_2$ 가 혼합된 시료의 경우 1173K 에서의 열처리 후 니켈 알루미네이트 또는 니켈 티타네이트와 같은 새로운 결정상의 생성이 관찰되었으나 $ZrO_2$가 혼합된 경우에는 새로운 결정상의 생성이 관찰되지 않았다. TPR 결과에 의하면, $Al_2O_3$ 또는 $TiO_2$를 혼합된 시료의 경우 벌크 NiO의 TPR 결과와는 달리 생성된 새로운 결정상에 기인한 여러 개의 환원 피크가 나타났으나 $ZrO_2$를 혼합한 경우 벌크 NiO와 비슷한 환원 피크를 보였다. TPR 결과를 기초로 Arrhenius plot 으로부터 각 혼합 산화물들의 수소 환원 활성화 에너지를 도출하였다. $ZrO_2$를 지지체로 사용하는 경우 다른 혼합 산화물들보다 지지체로서 안정한 혼합 산화물상을 형성한다는 것을 지시하듯이 상대적으로 가장 낮은 활성화 에너지를 나타냈다.

• 한국산학기술학회논문지
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• 제21권7호
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• pp.82-89
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• 2020

탄약내의 화약류 특히, 지연제의 지연시간에 대한 온도의 영향은 우리나라와 같이 연평균 최고최저 온도차가 뚜렷한 환경에서 충분히 존재할 수 있음에도 불구하고 이와 관련한 연구는 아직까지 국내에 보고된 바가 없다. 이에 본 연구는 우리나라 탄약류에 주로 사용되는 Zr/Ni계 지연제에 대해 주변 온도에 따른 연소속도 변화를 실험적으로 확인하였다. 이를 위해, K413 수류탄용 K414 신관에 Zr/Ni계 지연제를 충전하고 우리나라 기상환경을 고려한 주변 온도구간(-40 ℃ ~ 50 ℃)에서 온도변화에 따른 K414 신관의 지연시간 변화를 확인 및 분석하였다. K414 신관의 지연시간은 상기 시험 온도구간 내에서 시험온도를 10 ℃ 씩 변화시켜가며 측정하였고, 측정된 지연시간은 Zr/Ni계 지연제 충전 시에 기록한 지연제의 높이를 이용하여 연소속도로 환산되었다. 시험결과, Zr/Ni계 지연제의 지연시간은 주변 온도가 증가함에 따라 선형적으로 감소하는 경향이 있으며, Zr/Ni계 지연제 온도가 1 ℃ 상승할 때 마다 지연시간이 4.18 ms 감소하고, 연소속도는 2.73 mm/ms 로 빨라진 것으로 분석되었다. 즉, 연평균 최고최저 온도차이가 20 ℃ 이상인 주변 온도 환경에서는 약 80 ms 의 지연시간 차이가 발생하므로, Zr/Ni계 지연제의 시험평가 기준수립 시, 지연제가 노출된 주변 온도 조건을 반영한 지연시간이 고려되어야 할 것으로 사료된다.

• 자원환경지질
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• 제30권6호
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• pp.603-612
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• 1997

경상누층군이라 불리는 백악기 육성퇴적암-화산쇄설물들은 백악기 말-제3기초의 화강암류에 의해 관입 되어 있다. 의성-신령지역의 화강암류는 다양한 암상과 화학조성을 갖는다 : 반려암; 46.9, 섬록암; 58.3, 흑운모 화강암; 66.3~69.3, 장석 반암; 71.0 wt.% $SiO_2$. 화산암류는 화학적으로 금성산 칼데라에서는 안산암질 성분이 결여 된 현무암-유문암의 bimodal 유형과 선암산-화산 칼데라에서는 안산암-유문암의 felsic 유형으로 나뉜다. 대부분의 화성암류는 비알칼리 계열에 속하고, 칼크-알칼리 마그마의 분화 경로를 따른다. 화강암류는 높은 Zr/Y비에 의해 화산암류와 잘 구별된다. 화산암류에서 Zr/Y와 K/Y비의 차이는 맨틀기원 및 분별작용에서 불균질로 설명될 수 있다. 콘드라이트로 균질화된 희토류 원소량은 화강암류에서 Th와 K이 결핍되어 있고, 금성산 칼데라의 유문암에서 Sr와 Ti의 결핍되어 있다. 선암산-화산 칼데라의 유문암은 Rb, La 및 Ce이 부화되어 있다. $Rb-SiO_2$와 Rb-Y+Nb의 관계도는 화강암류와 화산암류가 화산호 환경이었음을 암시한다. K-Ar 연대는 4회의 심성활동 (섬록암; 89 Ma, 화강암; 64~62 Ma, 화강암/반암류; 55~52 Ma, 반려암; 52~45 Ma)으로 나뉘고, 금성산 칼데라의 bimodal 유형 (71~66 Ma)과 선암산-화산 칼데라의 felsic 유형 (61~54 Ma)으로 특징지워지는 화산활동이 수반되었다. 지화학 및 연대측정 자료들은 화성암류가 백악기말-제3기초 동안 다양한 지질학적 에피소드의 결과로 형성되었슴을 암시한다.

• 대한방사성의약품학회지
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• 제8권2호
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• pp.53-61
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• 2022

This study aimed to increase the targeting ability against PSMA in cell therapy using metabolic glycoengineering and biorthogonal chemistry and to visualize cell trafficking using PET imaging. Cellular membranes of THP-1 cells were decorated with azide(-N₃) using Ac₄ManNAz by metabolic glycoengineering. Engineered THP-1 cells were conjugated with DBCO-bearing fluorophore (ADIBO-Cy5.5) for 1 h at different concentrations and analyzed by confocal fluorescence microscopy and flow cytometry. For PSAM ligand conjugation to THP-1 cells, Ac₄ManNAz treated THP-1 cells were incubated with DBCO-PSMA ligand (ADIBO-GUL) at a final concentration with 100 µM for 1 h. To evaluate the effect on cell recognition, PSMA ligand conjugated THP-1 cells(as effectors) were co-cultured with PSMA positive 22RV1 (as target cells) at 3 : 1 a effector-to-target cell (E/T) ratio. The interaction between THP-1 and 22RV1 was monitored by confocal fluorescence microscopy. For preparing the radiolabeled THP-1, the cells were treated at the activity of ~ 740 kBq of [⁸⁹Zr]Zr(oxinate)₄/5 × 10⁶ cells. Radiolabeled cells were analyzed for determination of cell-associated radioactivity by gamma counting and viability using MTS assay. In the cytotoxicity assay, THP-1 cells did not have any cytotoxicity even when the Ac₄ManNAz concentration was 100 µM. In confocal microscopy and flow cytometry, THP-1 cells were efficiently labeled ADIBO-Cy5.5 in a dose-dependent manner, and the dose of 100 µM was the optimal concentration for the following experiments. The clusters of PSMA ligand-conjugated THP-1 cells and 22RV1 cells were identified, indicating cell-cell recognition over the cell surface between two types of cells. Cell radiolabeling efficiency was 54.5 ± 17.8%. THP-1 labeled with 0.09 ± 0.03 Bq/cell showed no significant cytotoxicity compared to unlabeled THP-1 up to 7 days. We successfully demonstrated that Ac₄ManNAz treated cells were efficiently conjugated with ADIBO-GUL for preparing the PSMA-targeting cells, and [⁸⁹Zr]Zr(oxinate)₄ could be used to label cells without toxicity. It suggested that PSMA-ligand conjugated cell therapy could be improved cell targeting and be monitored by PET imaging.