• 한국결정성장학회지
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• 제26권3호
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• pp.126-130
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• 2016

Ti-합금은 낮은 밀도, 낮은 탄성계수, 우수한 고온강도, 내산화성 및 인체적합성으로 자동차와 항공산업 및 바이오 산업에서 구조용 재료로 널리 연구되고 있다. 본 연구에서는 Ti-합금 중 대표적인 조성인 Ti-64(6 wt% Al, 4 wt% V) 합금에 대한 결정학적 특성과 미세조직에 대해서 알아보고자 하였다. XRD 분석을 통하여 Ti-64 샘플의 주요 결정상을 분석하였고, FE-SEM 및 EDX 분석을 통하여 Ti-64 합금 샘플의 미세구조를 화학조성의 차이에 의해 고찰하였다.

• 대한치과기공학회지
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• 제23권1호
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• pp.31-43
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• 2001

This study was performed to observe the micro-structure change of surface, behavior of oxide change of element, the component transformation of the alloy and the bonding strength between the porcelain interface in order to investigate effects of indium, tin on interfacial properties of porcelain fused to low gold alloy. Hardness of castings was measured with a micro-Vicker's hardness tester. The compositional change of the surface of heat-treated specimen was analyzed with an EDS and an EPMA. The interfacial shear bonding strength between alloy specimen and fused porcelain was measured with a mechanical testing system(MTS 858.20). The results were as follows: 1) The hardness value of alloy increased as increasing amount of indium addition. 2) The formation of oxidation increased as increasing indium and tin contents after heat treatment. 3) Diffusion of indium and tin elements increased as increasing indium and tin contents in metal-porcelain surface after porcelain fused to metal firing. 4) The most interfacial shear bonding strength was increased as increasing a composition of adding elements, and a heat-treatment time, and an oxygen partial pressure. From the results of this study it was found that the addition of alloying elements such as indium and tin increase hardness of as-cast alloy, produce surface oxide layer of adding elements by heat-treatment which may improve interfacial bonding strength between alloy and porcelain.

• 한국전기전자재료학회논문지
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• 제24권8호
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• pp.622-626
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• 2011

Lead-free piezoelectric ceramics with the composition of $(Na_{0.54}K_{0.46})_{0.96}Li_{0.04}(Nb_{1-0.10-x}Ta_{0.10}Sb_x)O_{3}$ (x= 0~8 mol%) were fabricated by nomal sintering at $1,090^{\circ}C$ for 5 h. the phase structure, microstructure and electrical properties were investigated with a emphasis on the influence of the Sb content. All samples exhibit a single perovskite phase over the whole compositional range. For the ceramics with x= 4 [mol%], two phase transitions are observed at $75^{\circ}C$ and $366^{\circ}C$, corresponding to the phase transitions of orthorhombic to tetragonal (To-t) and tetragonal to cubic (Tc), respectively. high electrical properties of $d_{33}$= 210.83 pC/N, kp= 40%, ${\varepsilon}_r$= 1,091.35, $\rho$= 4.54 g/$cm^2$ were obtained from the specimen with x= 4 [mol%], which suggests that the composition ceramics is a promising lead-free piezoelectric material.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2006년도 하계학술대회 논문집 Vol.7
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• pp.271-271
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• 2006

The structural, dielectric and piezoelectric properties of $[Bi_{1-x}(Na_{0.7-x}K_{0.2}Li_{0.1})]_{0.5}BaxTiO_3$ (BNKLBxT) ceramics were studied for the compositional range, x = 0-0.08. The samples were prepared by conventional sintering technique. The result of X-ray diffraction (XRD) suggest that $Ba^{2+}$ diffuse into the $[Bi(Na_{0.7}K_{0.2}Li_{0.1})]_{0.5}TiO_3$ (BNKLT) lattices to form a solid solution with a single phase perovskite structure. The ceramic show excellent piezoelectric and ferroelectric properties, and optimum properties measured are as follows: piezoelectric constant $d_{33}=230pC/N$, planar electromechanical coupling factor $k_p\;=\;40.3%$, remanent polarization $P_r\;=\;30\;{\mu}C/cm^2$, and coercive field $E_c\; =\;2.5\;kV/mm$, respectively.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2009년도 제38회 동계학술대회 초록집
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• pp.277-277
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• 2010

The capacity of the carbonaceous materials reached ca. $350\;mAhg^{-1}$ which is close to theorestical value of the carbon intercalation composition $LiC_6$, resulting in a relatively low volumetric Li capacity. Notwithstanding the capacities of carbon, it will not adjust well to the need so future devices. Silicon shows the highest gravimetric capacities (up to $4000\;mAhg^{-1}$ for $Li_{21}Si_5$). Although Si is the most promising of the next generation anodes, it undergoes a large volume change during lithium insertion and extraction. It results in pulverization of the Si and loss of electrical contact between the Si and the current collector during the lithiation and delithiation. Thus, its capacity fades rapidly during cycling. We focused on electrode materials in the multiphase form which were composed of two metal compounds to reduce the volume change in material design. A combination of electrochemically amorphous active material in an inert matrix (Si-M) has been investigated for use as negative electrode materials in lithium ion batteries. The matrix composited of Si-M alloys system that; active material (Si)-inactive material (M) with Li; M is a transition metal that does not alloy with Li with Li such as Ti, V or Mo. We fabricated and tested a broad range of Si-M compositions. The electrodes were sputter-deposited on rough Cu foil. Electrochemical, structural, and compositional characterization was performed using various techniques. The structure of Si-M alloys was investigated using X-ray Diffractometer (XRD) and transmission electron microscopy (TEM). Surface morphologies of the electrodes are observed using a field emission scanning electron microscopy (FESEM). The electrochemical properties of the electrodes are studied using the cycling test and electrochemical impedance spectroscopy (EIS). It is found that the capacity is strongly dependent on Si content and cycle retention is also changed according to M contents. It may be beneficial to find materials with high capacity, low irreversible capacity and that do not pulverize, and that combine Si-M to improve capacity retention.

• 한국응용과학기술학회지
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• 제25권2호
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• pp.211-218
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• 2008

The performance of positive plates depends on the structure of the lead dioxide active mass. The positive active materials (PAM) consists of a skeleton, built up of agglomerates and macropores. Agglomerates, in their turn, comprise particles and micropores. This paper described a study conducted to determine the effects of different soaking times between the acid fill and formation stages of the tubular plate production. For the positive plates a lead oxide were filled into tubular bag with a red lead. After filling the positive plates were soaked in $H_2SO_4$ solution. X-ray diffraction(XRD), scanning electron microscopy(SEM) and electrical testing had been used to study the compositional and morphological aspects of the positive active material(PAM) just prior and after formation. Results indicate that PAM compositions were effected by the soaking time and acid density of $H_2SO_4$ solution. It can be seen that as the soaking time duration increases, $\alpha$-PbO, $Pb_3O_4$, and Pb were all gradually sulphating. Composition of 3BS reached a maximum at around 3 h duration and $H_2SO_4$ of sp. gr. 1.10 on soaking. This results would suggest that the most beneficial conditions for soaking were the $H_2SO_4$ of sp. gr. 1.10 and 2 to 6 h of soaking.

• 한국광학회지
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• 제14권6호
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• pp.594-599
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• 2003

1.6 $\mu\textrm{m}$ 파장대의 U밴드 광증폭기용 광섬유 소재인 Pr첨가 Ge-Sb-Se 계열 셀레나이드 유리의 굴절률을 분광타원법을 이용하여 결정하였다. 시료의 광물성을 조사하기 위해 투과 파장 영역에서의 타원 스펙트럼을 Sellmeier 분산관계식에 기반한 공기/미시 거칠기층/표면층/기층으로 구성된 4상계의 모델에 적용하여 굴절률과 분산계수 및 박막구조상수를 동시에 얻을 수 있었다. 디스크 형태로 가공된 각 시료의 양면을 대상으로 위치에 따라 수회 반복 측정을 통하여 시료의 표면 거칠기의 영향을 파악함으로써 조성 변화에 대한 굴절률 변화 양상을 보다 정확히 파악하였다. 시료의 표면 거칠기가 굴절률 측정치의 편차에 주된 영향을 미쳤으나 1 몰%에 해당하는 소량의 조성변화에 따른 굴절률 변화를 신뢰할 수 있는 수준으로 결정할 수 있었다. 실험적으로 결정된 조성변화와 굴절률과의 관계식은 단일모드의 셀레나이드 광섬유 제작에 있어 코어와 클래드의 조성을 결정하는데 직접적으로 활용될 수 있다.

• 대한금속재료학회지
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• 제47권1호
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• pp.13-20
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• 2009

This work presents functionally graded coatings (FGC) of hydroxyapatite (HA) and metallic powders on Ti-6Al-4V implants using plasma spray coating method. HA has been the most frequently used coating material due to its excellent compatibility with human bones. However, because of the abrupt changes in thermomechanical properties between HA and the metallic implant across an interface, and residual stress induced on cooling from coating temperture to room temperature, debonding at the interface occurs in use sometimes. In this work, FGC of HA and Ti or Ti-alloy powders is made to mitigate the abrupt property changes at the interface and the effect of FGC on residual stress release is investigated by evaluating the mechanical bond strength between the implant and the HA coating layers. Thermal annealing is done after coating in order to crystallize the HA coating layer which tends to have amorphous structure during thermal spray coating. The effects of types and compositional ratio of metallic powders in FGC and annealing conditions on the bond strength are also evaluated by strength tests and the microstructure analysis of coating layers and interfaces. Finally, biocompatibility of the coating layers are tested under ISO 10993-5.

• 한국표면공학회지
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• 제34권5호
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• pp.435-444
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• 2001

WC-( $Ti_{1-x}$ A $l_{x}$) N coatings of constant changing Al concentration were deposited on S45C substrates by high-ionization sputtered PVD method. The Al concentration could be controlled by using evaporation source for Al and fixing the evaporation rate of the metals (i.e, WC- $Ti_{0.86}$A $l_{0.14}$N, WC- $Ti_{0.72}$A $l_{0.28}$N, and WC- $Ti_{0.58}$A $l_{0.42}$N). The corrosion behavior of WC-( $Ti_{1-x}$ A $l_{x}$)N coatings in a deaerated 3.5% NaCl solution was investigated by electrochemical corrosion tests and surface analyses. The measured galvanic corrosion currents between coating and substrate indicated that WC- $Ti_{0.72}$A $l_{0.28}$N coating showed the best resistance of the coating tested. The results of potentiodynamic polarization tests showed that the WC- $Ti_{0.72}$A $l_{0.28}$N coating deposited with 32W/c $m^2$ of Al target revealed higher corrosion resistance. This indicated that the WC- $Ti_{0.72}$A $l_{0.28}$N coating is effective in improving corrosion resistance. In EIS, the WC- $Ti_{0.72}$A $l_{0.28}$N coating showed one time constant loop and increased a polarization resistance of coating ( $R_{coat}$) relative to other samples. Compositional variations of WC-( $Ti_{1-x}$ A $l_{x}$)N coatings were analyzed by EDS and XRD analysis was performed to evaluate the crystal structure and compounds formation behavior. Surface morphologies of the films were observed using SEM and AFM. Scratch test was performed to measure film adhesion strength.strength. adhesion strength.strength.

• 한국결정성장학회지
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• 제17권2호
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• pp.82-89
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• 2007

붕규산염계 유리에 EAF Dust를 $40{\sim}80wt%$ 첨가하고 후 용융하여 유리를 제조한 후 $700^{\circ}C$/10hr으로 열처리하여 결정화유리 시편을 합성하였다. FT-IR, SEM, 그리고 EDS 분석을 통하여 조성 및 열처리 조건에 따른 시편내 결정상 및 결합상태 변화를 관찰하고, 이를 TCLP(Toxic Characterization Leaching Procedure) 실험에서 얻은 결과와 연계시켜 시편의 화학적 내구성을 연구하였다. 유리에 더스트 첨가량이 증가함에 따라 FT-IR 스펙트럼 상의 가교산소 진동피크($1050{\sim}1060cm^{-1}$)와 비가교산소 진동피크($960cm^{-1}$)가 합쳐진 넓은 피크($1000cm^{-1}$ 부근)가 저파수쪽으로 이동하였다. 동시에 boroxol ring의 $B_2O_3$ 구조가 tetrhedral-, trigonal- 그리고 di-borate로 변화되는 것을 확인하였다. 결정화유리 시편에서 Fe-O 피크가 확인되었으며 이는 spinel이 생성되었다는 XRD 결과와 일치하였다. TCLP를 행한 유리시편의 표면은 균열이 심하였으나 결정화유리는 큰 변화가 없어, 결정상 생성이 화학적 내구성을 향상시킴을 확인하였다. Fe의 용출량은 더스트가 80wt% 첨가된 결정화유리의 경우, 유리시편에 비하여 1/15로 감소하였다. Zn은 더스트 첨가량이 70wt% 이하인 결정화유리에서 용출량이 유리에 비해 높았으나 80wt% 이상 시편에서는 유리보다 감소하였고 이는 willemite 생성과 연관이 있는 것으로 사료된다.