• Title/Summary/Keyword: Sintered density

Search Result 1,250, Processing Time 0.029 seconds

Low Temperature Sintering Properties of the $0.6TiTe_3O_8-0.4MgTiO_3$ Ceramics with Sintering Adds (소결조제 첨가에 따른 $0.6TiTe_3O_8-0.4MgTiO_3$ 세라믹스의 jdhs 소결 특성)

  • Kim, Jae-Sik;Ryu, Ki-Won;Koh, Jung-Hyuk;Lee, Young-Hie
    • Proceedings of the KIEE Conference
    • /
    • 2007.11a
    • /
    • pp.114-115
    • /
    • 2007
  • In this study, low temperature sintering property of the $0.6TiTe_3O_8-0.4MgTiO_3$ ceramics with sintering adds were investigated for LTCC application which enable to cofiring with Ag electrode. $TiTe_3O_8$ mixed with $MgTiO_3$ to improve the temperature property. In the X-ray diffraction patterns, the columbite structure of $TiTe_3O_3$ phase and ilmenite structure of $MgTiO_3$ phase were coexisted in all specimens. In the case of $H_3BO_3$ addition, the bulk density and dielectric constant were decreased but quality factor was increased with amount of $H_3BO_3$ additions. The TCRF of the $0.6TiTe_3O_8-0.4MgTiO_3+xwt%H_3BO_3$ ceramics were moved to positive direction. In another case, SnO addition, the bulk density and dielectric constant were increased but Quality factor was decreased with amount of SnO additions. The TCRF of the $0.6TiTe_3O_8-0.4MgTiO_3$+ywt%SnO ceramics were shifted to negative direction. The dielectric constant, quality factor and TCRF of the $0.6TiTe_3O_8-0.4MgTiO_3$ ceramics with $2wt%H_3BO_3$ and 2.5wt%SnO sintered at $830^{\circ}C$ for 1h, were 28.5, 39,570GHz, $+9.34ppm/^{\circ}C$ and 29.86, 35,80000z, $-0.58ppm/^{\circ}C$, respectively.

  • PDF

Synthesis and Characterization of BaTiO3 Powder by Solid State Method (고상반응법을 이용한 BaTiO3 합성 및 특성 평가)

  • Kim, Yong Jin;Choi, Moon Hee;Shin, Hyo Soon;Ju, Byeong-Kwon;Chun, Myoung Pyo
    • Journal of the Korean Institute of Electrical and Electronic Material Engineers
    • /
    • v.33 no.6
    • /
    • pp.483-489
    • /
    • 2020
  • BaTiO3 powder was synthesized by a solid-state reaction using BaCO3 and TiO2. Different calcination temperatures (800℃, 850℃, 900℃, and 950℃) were set to investigate their effects on the properties of BaTiO3 powder. The synthesized BaTiO3 phase was confirmed to be a single phase by XRD, and the tetragonality (c/a) and crystallite size were calculated. Thereafter, each calcinated BaTiO3 was sintered at five different sintering temperatures (1,100℃, 1,150℃, 1,200℃, 1,250℃, and 1,300℃), and the tetragonality, density, porosity, dielectric constant, and grain size were measured. As the calcination temperature increased, the tetragonality and crystallite size also increased, to 1.008 and 66 nm, respectively, at 950℃. Moreover, most pellets showed increased density, dielectric constant, and tetragonality as the sintering temperature increased up to 1,250℃; the same parameters slightly decreased at 1,300℃. It is noteworthy that the tetragonality of BaTiO3 at 1,250℃ exhibits a very high c/a value of 1.0084. In addition, the grain size and dielectric constant measured near the Curie temperature increased as the sintering temperature increased.

Dielectric and Piezoelectric Properties of 0.95(K0.5Na0.5)NbO3-0.05Li(Sb0.8Nb0.2)O3 Ceramics according to the Amount of CuO Addition (CuO첨가에 따른 0.95(K0.5Na0.5)NbO3-0.05Li(Sb0.8Nb0.2)O3 세라믹스의 유전 및 압전특성)

  • Lee, Yu-Hyung;Kim, Do-Hyung;Yoo, Ju-Hyun;Kim, In-Sung;Song, Jae-Sung;Hong, Jae-Il
    • Journal of the Korean Institute of Electrical and Electronic Material Engineers
    • /
    • v.22 no.6
    • /
    • pp.489-494
    • /
    • 2009
  • In this study, In order to improve dielectric and piezoelectric properties of Lead-free piezoelectric ceramics, $0.95(K_{0.5}Na_{0.5})NbO_3-0.05Li(Sb_{0.8}Nb_{0.2})O_3+0.2\;wt%Ag_2O+0.4\;wt%MnO_2+Xwt%CuO$ were investigated as a function of the amount of CuO addition. With increasing the amount of CuO addition, density was increased up to 0.4 wt.% CuO and then decreased above. And also, electro mechanical coupling factor ($k_p$) was decreased. At the 0.4 wt% CuO added specimen sintered at $1020^{\circ}C$, $k_p$, Qm, density, dielectric constant (${\varepsilon}_r$) and $d_{33}$[pC/N] showed the optimal value of $4.37\;g/cm^3$, 0.354, 305, 645, and 144 pC/N respectively.

Effects of HA and TiN Coating on the Electrochemical Characteristics of Ti-6Al-4 V Alloys for Bone Plates

  • Oh, Jae-Wook;Choe, Han-Cheol;Ko, Yeong-Mu
    • Journal of Surface Science and Engineering
    • /
    • v.37 no.5
    • /
    • pp.249-252
    • /
    • 2004
  • Effects of HA and TiN coating on the electrochemical characteristics of Ti-6AI-4V alloys for bone plates were investigated using various test methods. Ti-6AI-4V alloys were fabricated by using a vacuum induction furnace and bone plates were made by laser cutting and polishing. HA was made of extracted tooth sintered and then tooth ash was used as HA coating target. The TiN and HA film coating on the surface were carried on using electron-beam physical vapor deposition (EB-PVD) method. The corrosion behaviors of the samples were examined through potentiodynamic method in 0.9% NaCI solutions at $36.5\pm$$1^{\circ}C$ and corrosion surface was observed using SEM and XPS. The surface roughness of TiN coated bone plates was lower than that of tooth ash coated plates. The structure of TiN coated layer showed the columnar structure and tooth ash coated layer showed equiaxed and anisotrophic structure. The corrosion potential of the TiN coated specimen is comparatively high. The active current density of TiN and tooth ash coated alloy showed the range of about $1.0xl0^{-5}$ $A\textrm{cm}^2$, whereas that of the non-coated alloy was$ 1.0xl0^{-4}$ $A\textrm{cm}^2$. The active current densities of HA and TiN coated bone plates were smaller than that of non-coated bone plates in 0.9% NaCl solution. The pitting potential of TiN and HA coated alloy is more drastically increased than that of the non-coated alloy. The pit number and pit size of TiN and HA coated alloy decreased in compared with those of non-coated alloy. For the coated samples, corrosion resistance increased in the order of TiN coated, tooth ash coated, and non-coated alloy.

Room-temperature tensile strength and thermal shock behavior of spark plasma sintered W-K-TiC alloys

  • Shi, Ke;Huang, Bo;He, Bo;Xiao, Ye;Yang, Xiaoliang;Lian, Youyun;Liu, Xiang;Tang, Jun
    • Nuclear Engineering and Technology
    • /
    • v.51 no.1
    • /
    • pp.190-197
    • /
    • 2019
  • W-K-TiC alloys with different titanium carbide concentrations (0.05, 0.1, 0.25, 0.5, 1, 2) wt.% were fabricated through Mechanical Alloying and Spark Plasma Sintering. The effects of the addition of nano-scaled TiC particles on the relative density, Vickers micro-hardness, microstructure, crystal information, thermal shock resistance, and tensile strength were investigated. It is revealed that the doped TiC nano-particles located at the grain boundaries. The relative density and Vickers micro-hardness of W-K-TiC alloys was enhanced with TiC addition and the highest Vickers micro-hardness is 731.55. As the TiC addition increased from 0.05 to 2 wt%, the room-temperature tensile strength raised from 141 to 353 MPa. The grain size of the W-K-TiC alloys decreased sharply from $2.56{\mu}m$ to 330 nm with the enhanced TiC doping. The resistance to thermal shock damage of W-K-TiC alloys was improved slightly with the increased TiC addition.

Effect of Calcination Temperature on Ionic Conductivity of All-solid State Battery Electrolytes (하소 온도가 전고체 전지 전해질의 이온전도도에 미치는 영향)

  • Yu Taek Hong;Ji Min Im;Ki Sang Baek;Chan Gyu Kim;Seung Wook Baek;Jung Hyun Kim
    • New & Renewable Energy
    • /
    • v.20 no.2
    • /
    • pp.71-81
    • /
    • 2024
  • In this study, the electrochemical properties of garnet-structured all-solid-state battery electrolytes (Li6.4La3Zr1.4Ta0.6O12, hereafter LLZTO) were assessed by altering the calcination temperature, while maintaining a consistent sintering duration. Among the various heat treatment conditions employed for sample fabrication, the '700_1100' condition, denoting a calcination temperature of 700℃ and a sintering temperature of 1100℃, resulted in the most exceptional ionic conductivity of 4.89 × 10-4 S/cm and a relative density of 88.72% for the LLZTO material. This is attributed to the low calcination temperature of 700℃, leading to reduced grain size and enhanced cohesiveness, thus resulting in a higher sintered density. In addition, a microstructure similar to the typical sintering characteristics observed in Spark Plasma Sintering (SPS) methods was identified in the SEM analysis results under the '700_1100' condition. Consequently, the '700_1100' heat treatment condition was deemed to optimal choice for enhancing ionic conductivity.

Fabrication of high-entropy alloy superconducting thin films via pulsed laser deposition technique

  • Soon-Gil Jung;Jeongwon Noh;Yoonseok Han;Woo Seok Choi;Won Nam Kang;Tuson Park
    • Progress in Superconductivity and Cryogenics
    • /
    • v.26 no.3
    • /
    • pp.27-31
    • /
    • 2024
  • We fabricate high-entropy alloy (HEA) Ta1/6Nb2/6Hf1/6Zr1/6Ti1/6 superconducting (SC) thin films via a pulsed laser deposition method. Two targets are prepared using arc melting, each followed by sintering at different temperatures: 550℃ and 700℃ for 12 hours. The films, HEA550 and HEA700, are deposited on c-cut Al2O3 substrates at a substrate temperature of 520℃, using the targets sintered at 550℃ and 700℃, respectively. The SC transition temperature (Tc) of HEA700 is 6.88 K, slightly higher than that of HEA550 (= 6.27 K). Both films exhibit similar upper critical field (Hc2) at 0 K, with 11.34 T for HEA550 and 11.40 T for HEA700. Notably, HEA700 exhibits a large critical current density (Jc) of approximately 4.4 MA/cm2 and 3.5 MA/cm2 at 2.0 K and 4.2 K, respectively, accompanying by a predominance of normal point pinning. These results indicate that the targets prepared by arc melting are beneficial for achieving a large Jc in HEA SC thin films, thus providing new avenues for improving SC critical properties of HEA thin films for their practical applications.

Consolidation of Segment Powder for Diamond Tool by Magnetic Pulsed Compaction (자기펄스 압축성형법에 의한 다이아몬드 공구용 세그먼트 분말 성형)

  • Yun, J.S.;Lee, J.G.;Lee, M.K.;Rhee, C.K.;Park, M.S.;Hong, S.J.
    • Journal of Powder Materials
    • /
    • v.15 no.5
    • /
    • pp.378-385
    • /
    • 2008
  • This article presents the successful consolidation of the mixed Co and Diamond powders for a drilling segment by the combined application of magnetic pulsed compaction (MPC) and subsequent sintering, and their properties were analyzed. Homogeneous hardness (Hv 220) and density (97%) of sintered bulks fabricated by MPC were obtained by the new technique, where higher pressure has been employed for short period of time than that of general process. A fine microstructure and homogeneous hardness in the consolidated bulk were observed without cracks. Relatively higher drilling speed of 9.61 cm/min and life time of 6.55 m were found to the MPCed specimens, whereas the value of the specimens fabricated by general process was 11.71 cm/min and 7.96 m, respectively. A substantial improvement of mechanical properties of segment was achieved through this study.

Recycling Method of Used Indium Tin Oxide Targets (폐 인듐주석산화물 타겟의 재활용 기술)

  • Lee, Young-In;Choa, Yong-Ho
    • Korean Journal of Materials Research
    • /
    • v.22 no.4
    • /
    • pp.174-179
    • /
    • 2012
  • In this study, we demonstrated a simple and eco-friendly method, including mechanical polishing and attrition milling processes, to recycle sputtered indium tin oxide targets to indium tin oxide nanopowders and targets for sputtered transparent conductive films. The utilized indium tin oxide target was first pulverized to a powder of sub- to a few- micrometer size by polishing using a diamond particle coated polishing wheel. The calcination of the crushed indium tin oxide powder was carried out at $1000^{\circ}C$ for 1 h, based on the thermal behavior of the indium tin oxide powder; then, the powders were downsized to nanometer size by attrition milling. The average particle size of the indium tin oxide nanopowder was decreased by increasing attrition milling time and was approximately 30 nm after attrition milling for 15 h. The morphology, chemical composition, and microstructure of the recycled indium tin oxide nanopowder were investigated by FE-SEM, EDX, and TEM. A fully dense indium tin oxide sintered specimen with 97.4% of relative density was fabricated using the recycled indium tin oxide nanopowders under atmospheric pressure at $1500^{\circ}C$ for 4 h. The microstructure, phase, and purity of the indium tin oxide target were examined by FE-SEM, XRD, and ICP-MS.

Mullite Formation and Effect in Porcelain Body by Replacing Kaolinite with Pyrophyllite (납석으로 카올린을 대체한 도자기 소지의 뮬라이트 형성과 특성)

  • Kwak, An-Na;Kim, Geun-Hee;Pee, Jae-Hwan;Kim, Jong-Young;Cho, Woo-Seok;Kim, Kyeong-Ja;Lee, Jong-Keun
    • Journal of the Korean Ceramic Society
    • /
    • v.49 no.3
    • /
    • pp.216-220
    • /
    • 2012
  • Mullite formation in a porcelain body was promoted extensively by replacing kaolinite with pyrophyllite. Effects of mullite formation and vitrification by substitution of kaolinite with pyrophyllite on the mechanical and thermal properties were investigated. Addition of 45-55% pyrophyllite (pyrophyllite (45-55%)-feldspar (30%)-Gairome clay (20%)) could vitrify the sintered samples (water absorption : 0.05%, bulk density : 2.66g/cc) and improve the flexural strength (122MPa) when fired at $1280^{\circ}C$. Mullite formation was found to be decreased with increasing content of pyrophyllite. On the contrary, beyond 50% of pyrophyllite quartz and cristobalite phases was found to be increased. Thermal expansion coefficient of the samples decreased with increase of mullite phase. In triaxial system of pyrophyllite-feldspar-clay, the mullite formation of the samples with 50% pyrophyllite reaches about 78.7% and thermal expansion coefficient was found to be $5.4{\times}10^{-6}/K$.