• Title/Summary/Keyword: Ceramic products

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The Solid State Bonding or ZrO2/NiTi: (I) Optimizating of Bonding Condition and its Strength (ZrO$_2$와 NiTi 합금의 고상접합 : (I)접합의 최적조건 및 접합강도)

  • Kim, Young-Jung;Kim, Hwan
    • Journal of the Korean Ceramic Society
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    • v.28 no.8
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    • pp.654-660
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    • 1991
  • Stabilized Zirconia (3 mol % Yttria, 3Y-TZP) was joined with intermetallic compound NiTi which has similar thermal expansion coefficient. The optimum bonding condition was determined by the Taguchi Method. Under the optimum bonding condition, the 4-point bending strength was as high as 400 MPa. bonding interfaces were examined by optical microscope, SEM, and TEM; reaction products were identified by XRD and TEM, The relationship between products and strength was examined.

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Characterization of LaCrO$_3$ Powders Synthesized by Combustion Process with Different Heating Methods (가열방법에 따른 LaCrO$_3$ 연소합성분말의 특성)

  • 정층환;박홍규;오석진;박지연
    • Journal of the Korean Ceramic Society
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    • v.35 no.10
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    • pp.1078-1084
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    • 1998
  • lanthanum chromite(LaCrO3) powder was synthesized by the combustion of a solution of metal nitrates La(NO3).6H2O and Cr(NO3)3.9H2O and urea. The pH of solution affected a yield of the combustion products but did not influence the morphology of the products. When the pH of the solution was in the range of 0.7-4, the yield of the combustion products was more than 90% The morphology of the combustion products was af-fected by heating methods for the solution. The hot-plate induced heating of the solution yielded powders hav-ing two-dimensionally interconnected agglomerates whereas microwave-induced heating produced a fine and non-agglomerated powders. The specific surface area(BET) of the combustion products using microwave-in-non-agglomerated powders. The specific surface area(BET) of the combustion products using microwave-in-duced heating method were larger(25~32m2/g) than that of hot plate heating method(10-14m2/g)

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Synthesis of Analcime from Domestic Bentonite (국산 Bentonite로부터 Analcime합성)

  • 노훤주;주충열;김면섭
    • Journal of the Korean Ceramic Society
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    • v.16 no.4
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    • pp.201-205
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    • 1979
  • Domestic Yungil bentonite (montmorillonite) was treated with 1N sodium hydroxide solution in an autoclave at several temperatures, between 100 to 200℃, for 1 to 24 hrs. The products were examined by X-ray diffraction analysis. The following concecutive reaction was valid. montmorillonite→amorphous aluminosilicate→analcime The reaction rate constants k and k' at 200℃ were 0.35hr-1 and 0.22hr-1, respectively. The activation energies for the conversion from montmorillonite to amorphous aluminosilicate and from amorphous aluminosilicate to analcime were 10 kcal/mol and 12kcal/mol, respectively.

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Nitridation of Silicon Powder Compacts in Air (Air 분위기에서 규소성형체의 질화반응)

  • 최석홍;안영필
    • Journal of the Korean Ceramic Society
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    • v.25 no.4
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    • pp.380-384
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    • 1988
  • This investigation includes nitridation phenomena of silicon powder compacts in air. Nitridation reaction condition has been provided with using silicon nitride bed and active carbon additive. Reaction products are Oxynitride, $\alpha$-Si3N4, and $\beta$-Si3N4, Oxynitride(Si2N2O) phase in formed at outer surface layer ofsilicon powder compacts. $\alpha$-Si3N4, and $\beta$-Si3N4 are formed at inner region of powder compacts. Microstructural observation indicates that nitridation mechanism in this work is the same as conventional nitridation mechanism nitrogen gas.

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Mechanical Properties of Sintered and HIPed Silicon Nitride (상압소결과 열간정수압소결 질화규소의 기계적 성질)

  • 김창삼;하정수;이준근
    • Journal of the Korean Ceramic Society
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    • v.24 no.3
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    • pp.223-226
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    • 1987
  • Among many densification routes for silicon nitride, HIP(hot isostatic pressing) is becomming more popular these days, mainly due to the fact that it can produce highly reliable products with superior mechanical properties. This study involves in sintering of silicon nitride followed by HIP which requires no canning. Various property changes curing sintering and HIP are observed and analyzed in terms of microstructural changes. Porosity decrease and enhanced interlocking of grains by HIP are considered to be the major causes for improved mechanical properties of silicon nitride.

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On Crystallization of Hadong Kaolin Granulated Cylindrically Treated with Aqueous Sodium Hydroxide Solution (원주형으로 성형된 하동고령토의 수산화나트륨 수용액 처리에 의한 결정의 변화)

  • 김면섭
    • Journal of the Korean Ceramic Society
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    • v.15 no.1
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    • pp.21-27
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    • 1978
  • Hadong Kaolin (Halloysite) was granulated cylindrically and treated with 1N aqueous sodium hydroxide solution for 6-48 hrs at 60-10$0^{\circ}C$. The crystalling structure of surface of the products was studied by X-ray powder diffraction method. The reaction rate of halloysite to sodium A zeolite showed a gradual decrease from surface to inner layer. At the surface layer, the reaction mechanism was observed as first order consecutive reaction as follows: halloysitelongrightarrowamorphous aluminosilicatelongrightarrowsodium A zeolitelongrightarrowhydroxysodalite By applying the above reaction mechanism, the rate constants and activation energies was measured.

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A Study on Reaction Products between Cokes and Kaolinites (국산 cokes를 이용한 고급복합내화재료개발에 관한 연구)

  • 이희수;박정현;오영제
    • Journal of the Korean Ceramic Society
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    • v.15 no.1
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    • pp.28-34
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    • 1978
  • In order to develop the high refractory composite materials consisting of mullite and carborundum, Hadong kaolin and coal coke were selected as the starting materials. Silicone carbide crystals formed during the high-temperature reaction between kaolin and coke were detected by X-ray diffraction method and identified by electron diffraction. The temperature at which the amorphous silicone carbide begins to crystallize could be assumed to be about 155$0^{\circ}C$, which is the lower temperature claimed by others.

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Synthesis of Analcime by Treating of Domestic Feldspar (국산 장석으로부터의 Analcime합성)

  • 김면섭
    • Journal of the Korean Ceramic Society
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    • v.14 no.1
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    • pp.7-11
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    • 1977
  • Domestic Anyang feldspar was treated in autoclave with 1N sodium hydroxide solution for 1-6 hrs at 100-20$0^{\circ}C$ By X-ray diffraction patterns and cation exchange capacity, the products were examined. The following concecutive reaction was valid. AlbitelongrightarrowAmorphous aluminosilicatelongrightarrowAnalcime The reaction rate constants, k1 and k2, were 0.20 and 0.15(1/hr) at 20$0^{\circ}C$ respectively. The activiation energy from albite to amorphous aluminosilicate was 10 kcal/mol, and from amorphous aluminosilicate to analcine 13 kcal/mol. The analcime obtained was excellent in cation exchange capacity, amounting to 210meq./100g.

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A Study on the Influence of ZinC Chloride In Portland Cement Hydration Reaction (포틀랜드 시멘트 수화반응에 있어 Znic Chloride의 영향에 관한 연구)

  • 정현구;이경희;조재우;이재원
    • Journal of the Korean Ceramic Society
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    • v.37 no.7
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    • pp.681-685
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    • 2000
  • The influence of ZnCl2 in portland cement hydration was studied. The hydration reaction was progressed with ZnCl2 solution to observe the adiabatic hydration exothermic and hydration products. To compare with cement hydration, Ca(OH)2 solution reacted with ZnCl2 was carried out. The addition of ZnCl2 solution to the portland cement was retarded hydration quantitatively. Because ZnO which was produced in certain pH adsorbed with unhydrated cement made retarded the hydration reaction.

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Oxidation Behavior of $\beta$-Sialon ($\beta$-Sialon 소결체의 산화 거동)

  • 박용갑;장병국
    • Journal of the Korean Ceramic Society
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    • v.26 no.3
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    • pp.341-346
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    • 1989
  • In order to evaluate the oxidation behavior of $\beta$-Sialon, $\beta$-Sialon ceramics was prepared from Si3N4, Al2O3, AlN and Y2O3 system. The specimens were oxidized in an oxygen atmosphere at 1, 20$0^{\circ}C$ for 9days. Oxidation behavior was evaluated by weight gain oxidation process, surface roughness. Microscopy, EDX and X-ray diffraction analysis were also used for the evaluation. The weight and surface roughness ofoxidized specimens were increased with increasing the oxidation time. Oxidized products were mullite, $\alpha$-cristobalite, yttrium aluminum oxide and yttrium silicate oxide.

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