• 한국산학기술학회논문지
• /
• 제4권4호
• /
• pp.341-345
• /
• 2003

ZnWO₄는 높은 품질계수에 의해 주파수 선택성이 뛰어나지만 다층형태의 고주파 무선부품으로의 응용을 위해서는 높은 소결온도(1100℃), 큰 음의 공진주파수 온도계수(-70ppm/℃), 낮은 유전율(15.5) 등에 대한 보정이 필요하다. 본 연구에서는 ZnWO₄에 TiO₂및 LiF를 첨가하여 ZnWO₄의 저손실특성을 유지하면서 주파수 온도안정성 및 저온소결성을 부여하고자 하였다. 큰 양의 공진주파수 온도계수(＋400ppm/℃) 및 유전율(100)을 갖는 TiO₂의 첨가는 공진주파수 온도계수를 음의 값에서 양의 값으로 변화시켰으며 유전율의 증가를 가져왔다. TiO₂를 20 mol％ 첨가한 경우 공진주파수 온도계수가 0에 가깝고 유전율 19.4에 품질계수 50000㎓의 특성을 얻을 수 있었으나 소결온도는 1100℃로 높은 소결온도를 보였다. ZnWO₄에 TiO₂가 첨가된 혼합체에 LiF의 첨가는 액상형성에 의해 소결온도를 1100℃에서 850℃로 크게 저하시킬 수 있었다. LiF는 첨가는 LiF 자체의 큰 공진주파수 온도계수에 의해 온도계수를 음의 값으로 변화시켰다. 따라서 TiO₂및 LiF의 적당량의 첨가는 온도 안정성을 갖는 저손실 ZnWO₄-TiO₂-LiF 계 LTCC(Low Temperature Confined Ceramics) 소재를 제조할 수 있었다.

• 한국세라믹학회지
• /
• 제22권1호
• /
• pp.11-18
• /
• 1985

The effect of stress induced phase transformation on $Al_2 O_3$ matrix dispersed with $ZrO_2-Y_2O_3$ has been studied. In order to determinate the mechanical properties three $Al_2O_3-ZrO_2$ composite series containing 1, 3 and 5 mole% $Y_2O_3$ were prepared. The starting materials were $Al_2O_3$ and $ZrO_2-Y_2O_3$ which was prepared from the aqueous solution of high purity $YCl_3$.$6H_2O$ and $ZrOCl_2$.$8H_2O$. Powder mixtures of $Al_2O_3-ZrO_2$ containing $Y_2O_3$ have been prepared by ball-milling with methanol and the samples were formed by isostatic press and sintered at 150$0^{\circ}C$ for 2hrs. After sintering. the specimens were polished for mechanical determination. The relative density of sintered specimens were also measured. It was found that the addition of 1, 3mole% to {{{{ { ZrO}_{2 } }} allowed full retention of the tetragonal phase in $Al_2O_3-ZrO_2$ but partially stabilized zirconia (PSZ) was produced by additions of 5 mole% $Y_2O_3$.The critical stress-intensity factor KIc of $A_2O_3-ZrO_2$ (containing 1 mole% $Y_2O_3$) composite materials increased with increasing $ZrO_2$ content, The maximum value of KIC=7Mn/$m^3$/2 at 20 mole% $ZrO_2$ exhibited about twice that of the $Al_2 O_3$ The modulus of rupture exhibited a trend similiar to KIC The maximum value of MOR was 580MN/m2. As the amount of Y2O3 increase it was observed that the maximum of KIC and MOR decreased : Additions of 3 mole% $Al_2O_3$ $Y_2O_3$ allowed the maximum of KIC 6MN/$m^3$/2 MOR 540MN/$m^2$ at 15 mole% $ZrO_2$ additions of 5 mole% $Y_2O_3$ allowed the maximum of KIC 5MN/$m^3$/2 MOR 410MN/$m^2$ at 10 mole% $ZrO_2$.

• 한국세라믹학회지
• /
• 제44권6호
• /
• pp.291-296
• /
• 2007

Porous $Al_2O_3-(m-ZrO_2)$ composites were fabricated by pressureless sintering, using different volume percentages (40% - 60%) of poly methyl methacrylate (PMMA) powders as a pore-forming agent. The pore-forming agent was successfully removed, and the pore size and shape were well-controlled during the burn-out and sintering processes. The average pore size in the porous $Al_2O_3-(m-ZrO_2)$ bodies was about $200\;{\mu}m$ in diameter. The values of relative density, bending strength, hardness, and elastic modulus decreased as the PMMA content increased; i.e., in the porous body (sintered at $1500^{\circ}C$) using 55 vol % PMMA, their values were about 50.8%, 29.8 MPa, 266.4 Hv, and 6.4 GPa, respectively. To make the $Al_2O_3-(m-ZrO_2)$/polymer hybrid composites, a bioactive polymer, such as PMMA, was infiltrated into the porous $Al_2O_3-(m-ZrO_2)$ composites. After infiltration, most of the pores in the porous $Al_2O_3-(m-ZrO_2)$ composites, which were made using 60 vol % PMMA additions, were infiltrated with PMMA, and their values of relative density, bending strength, hardness, and elastic modulus remarkably increased.

• 전기학회논문지
• /
• 제60권12호
• /
• pp.2270-2275
• /
• 2011

The sintering behavior and microwave properties of ferrite ($Ba_3Co_{2-2x}Zn_{2x}Fe_{24}O_{41}$ ceramics) were investigated for microwave applications. Also PIFA type antenna with ferrite was simulated. All samples were prepared by the solid state reaction method and sintered at $1350^{\circ}C$. All ceramics had relatively density above of 92% compare with theoretical density of $Ba_3Co_2Fe_{24}O_{41}$ ceramics. From the XRD pattens, the Z-type phase was existed as main phase in $Ba_3Co_{2-2x}Zn_{2x}Fe_{24}O_{41}$ ceramics. The permittivity and permeability of $Ba_3Co_{2-2x}Zn_{2x}Fe_{24}O_{41}$ ceramics were increased with Zn additions and decreased rapidly over frequency of 200~600 MHz. Several PIFA type antennas with ferrite and FR4 were simulated. All antenna structure had return loss of less than -10 dB at each resonant frequency. Simulated antenna using both ferrite and FR4 showed size reduction of 25% without a significant decrement of efficiency.

• 한국재료학회:학술대회논문집
• /
• 한국재료학회 2003년도 추계학술발표강연 및 논문개요집
• /
• pp.113-113
• /
• 2003

고체전해질체로 사용되는 산소이온전도체로는 $Y_2$O$_3$ 안정화 ZrO$_2$가 널리 연구되어 왔고, 실질적으로 많이 사용되고 있다. 그러나 특히 대전력을 얻고자 하는 고체전해질 연료전지 분야에 있어서는 다른 재료를 찾고자 하는 많은 노력이 이루어지고 있다. 이에 CeO$_2$계 세라믹스는 ZrO$_2$계보다 낮은 온도에서 더 높은 이온전도도를 가지고 있어 많은 주목을 받고 있다. 그러나 이 CeO$_2$계를 소결시키는 데는 1$600^{\circ}C$이상의 고온을 필요로 한다. 이 런 고온의 소결온도를 낮추기 위한 방안으로는 균일하고 미세한 출발원료를 사용하거나 소결조제를 첨가하는 것 등이 있다. 균일하고 미세한 출발원료를 제조하는 연구는 국내외에서 많이 이루어지고 있으나 소결조제 첨가에 대한 연구는 별로 이루어진게 없다. 다만 국외에서 Co$_3$O$_4$, Fe$_2$O$_3$, CoO 첨가에 의한 연구가 최근에 이루어지고 있으며, 본 연구실을 중심으로 Ga$_2$O$_3$, $Al_2$O$_3$ 첨가에 대한 연구가 이루어지고 있다. 본 연구실에서는 그간 공침법으로 제조되는 소결조제 첨가 Gd$_2$O$_3$-doped CeO$_2$ 분말을 사용하여 소결조제 첨가효과를 살펴보았다.

• 한국세라믹학회지
• /
• 제32권10호
• /
• pp.1194-1202
• /
• 1995

The influences of TiC additions to the α-SiC on microstructural, mechanical, and electrical properties were investigated. Electrical discharge machinability of SiC-TiC composites was also studied. Samples were prepared by adding 30, 45, 60 wt.% TiC particles as a second phase to a SiC matrix. Sintering of SiC-TiC composites was done by hot pressing under a vacuum atmospehre from 1000 to 2000℃ with a pressure of 32 MPa and held for 90 minutes at 2000℃. Samples obtained by hot pressing were fully dense with the relative densities over 99% except 60wt.% TiC samples. Flexural strength and fracture toughness of the samples were increased with the TiC content. In case of SiC samples containing 45 wt.% TiC, the fracture toughness showed 90% increase compared to that of monolithic SiC sample. The crack propagation and crack deflection were observed with a SEM for etched samples after Vicker's indentation. The electrical resistivities of SiC-TiC composites were measured utilizing the four-point probe. The electrical dischage machining of composites was also conducted to evaluate the machinability.

• 한국재료학회지
• /
• 제8권11호
• /
• pp.1043-1047
• /
• 1998

CuO 및 C얘의 첨가가 $BiNbO_4$ 세라믹스의 고주파 유전특성에 미치는 영향을 조사하였다. CdO 첨가량이 증가함에 따라 소결밀도 및 품질계수는 감소하였고 소결온도가 증가하면 유전상수 및 품질계수는 증가하였다. $BiNbO_4$에 CuO 및 CdO를 각각 0.03wt% 첨가한 시편을 $960^{\circ}C$에서 소결시 유전율 41.2, 품질계수($Q{\times}f_0$) 6,500(at 5.6GHz), 공진주파수 온도계수 $3ppm^{\circ}C$의 우수한 고주파 유전특성을 얻을 수 있었다.

• 한국표면공학회:학술대회논문집
• /
• 한국표면공학회 2012년도 추계총회 및 학술대회 논문집
• /
• pp.7-11
• /
• 2012

Plasma electrolytic oxidation of magnesium alloys is a well known technique to produce corrosion and wear resistant coatings. The addition of particles to the electrolyte provides a possibility to produce coatings with an increasing range of composition by in-situ incorporation of those particles into the coating. An extensive literature review has revealed that the mode of incorporation depends mainly on the melting point of the used particles and the energy provided by the discharges of the PEO process. The spectrum ranges from inert to partly reactive incorporation, but a complete reactive incorporation and a formation of a new single phase coating was not observed so far. Thus a new approach in PEO processing is introduced using specific particles as a kind of sintering additive, changing not only the composition but lowering the melting temperature and increase the liquid phase fraction during the discharges, resulting in a new amorphous coating.

• 한국세라믹학회지
• /
• 제27권6호
• /
• pp.799-807
• /
• 1990

In this study, effects of oxide additives on mechanical properties and microstructure of A1N and A1N polytype ceramics were investigated. Fine A1N powder was synthesized by nitriding alumiuim hydroxide prepared from Al-isopropoxide, at 1350$^{\circ}C$ for 10h in N2 atmosphere. By adding 3w/o Y2O3, 0.56w/o CaO, and 10w/o SiO2 to AlN powder, AlN and AlN polytype ceramics were prepared by hot-pressing under the pressure of 30 MPa at 1800$^{\circ}C$ for 1h. AlN ceramics with no additives formed considerable amount of AlON phase, while AlN ceramics doped with Y2O3 or CaO decreased AlON phase and formed Y-Al or Ca-Al oxide compound. AlN＋10w/o SiO2(＋3w/o Y2O3) composition produced AlON and AlN polytype compound having 21R as a major phase. Room temperature flexural strength of AlN ceramics with no additive was 246MPa, and room temperature flexural strength and critical temperature difference by thermal shock(ΔTc) of AlN ceramics dooped with Y2O3 or CaO were 532MPa/340$^{\circ}C$ and 423MPa/300$^{\circ}C$, respectively. Y2O3 and CaO used as sintering agent played roles of densification and oxygen removal of AlN ceramics, and affected grain growth/grain morphologies of AlN ceramics.

• 한국세라믹학회지
• /
• 제28권10호
• /
• pp.767-776
• /
• 1991

Effects of the additions of SiB4 as burnable poison to UO2 on the green density, densification, interdependence between density-grain growth and microstructure of sintered UO2 were studied. UO2 pellets were sintered in flowing hydrogen, at temperature 1200, 1350, 1500, and 168$0^{\circ}C$ for 3 hours and at 168$0^{\circ}C$ for 0, 1, 3, and 10 hours, respectively. Green densities were in the range of about 4.5~5.4 g/㎤, and decreased as the amount of SiB4 increased when green pellets were made by with use of a double action press at 1000 kg/$\textrm{cm}^2$. The density of sintered UO2 pellets was around 92~94% of the theoretical density and did not change significantly as the amount of SiB2 addition increased. However, the density of sintered pellets decreased with the increase in SiB4. The grain growth could be characterized in terms of two stages: Grain growth occurred with the increasing density in the first stage, whereas the second stage was characterized by the grain growth without increasing of density. A liquid phase was observed at grain boundaries and grain edges in the microstructure of sintered UO2 pellets with 5000 ppm and 10,000 ppm SiB4. This liquid, possible formed at about 168$0^{\circ}C$, did not enhance the shrinkage, but appeared to accelarate the grain growth. It seems that the second stage grain growth was due to the presence of pressurized insoluble trapped gas in isolated pores.