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유기용매의 사용없이 알콕사이드로부터 코디어라이트 분말제조
류수착,김호룡,김겸,박희찬,Ryu, S.C.,Kim, H.R.,Kim, K.,Park, H.C. 한국세라믹학회 1994 한국세라믹학회지 Vol.31 No.3
Cordierite powders were prepared by controlled hydrolysis of metal alkoxides with catalysts in water medium without using organic solvents. Water was adjusted to a certain pH by HC1 and NH4OH. $\alpha$-Cordierite powder was prepared from aluminum isopropoxide, tetraethyl orthosilicate and magnesium ethoxide mixed with water adjusted to pH of 3. At water pH of 11, $\alpha$-cordierite, mullite and $\beta$-quartz phases were coexisted. The powders were freeze dried, calcined and then fired at different temperatures. The characteristics of powders were examined by means of DTA, X-ray diffraction, FT-IR, and electron microscopy. It was found that $\alpha$-cordierite could be synthesized at temperature of 120$0^{\circ}C$ from the powders prepared by alkoxides with water medium without organic solvents.
코오디어라이트 세라믹의 유전상수에 미치는 기공율의 영향
류수착,박희찬,Ryu, Su-Chak,Park, Hui-Chan 한국재료학회 1996 한국재료학회지 Vol.6 No.2
물과 에탄올의 혼합용액에 HCI을 촉매로하여 금속알콕사이드의 가수분해로부터 코오디어라이트 분말을 제조하였다. 이때 HCI/precursor 몰비로써 촉매의 양을 조절하였다. 건조분말 중의 용매를 제거하기위해 80$0^{\circ}C$에서 3시간 하소처리하였다. 이들 하소된 분말에 대하여 시차열분석과 X-선회절분석을 행한 결과-92$0^{\circ}C$에서 $\mu$-cordierite, -103$0^{\circ}C$에서 $\alpha$-cordierite 결정상의 생성을 확인하였다. 또한, 하소분말을 가압성형한 후 130$0^{\circ}C$에서 4시간 열처리한 결과 HCI양에 따라 기공율 19.45-25.45%, 부피비중 2.06-1.70g/㎤, 유전상수 1.38-3.38 범위의 소결체를 얻었다. HCI양이 증가할수록 기공율은 증가한 반면에 비유전상수와 부피비중은 감소하였다.
굴패각으로부터 제조된 $\textrm{Al}_2\textrm{O}_3$-CaO내화물의 특성
류수착,박홍채,Ryu, Su-Chak,Park, Hong-Chae 한국재료학회 1998 한국재료학회지 Vol.8 No.1
알루미나와 하소된 귤껍질의 소결반응에 의해 A $I_{2}$ $O_{3}$-CaO내화물이 제조되었다. 치밀화과정에서의 CaO의 영향과 A $I_{2}$ $O_{3}$-CaO 소결체의 특성을 고찰하였다. 소결체의 미세구조와 EDS 결과로 A $I_{2}$ $O_{3}$-CaO화합물을 확인하였다. 145$0^{\circ}C$에서 열처리한 소결체는 2.87/㎤의 부피비중과 12.03%의 겉보기 기공율을 가지며 압축강도는 312kg/$\textrm{cm}^2$이였다. 140$0^{\circ}C$에서 서결체의 열팽창 계수는 6.55Kx10$_{-6}$ $K_{-1}$이였다.
$\textrm{TiO}_2$ 첨가량에 대한 알루미나 세라믹스의 특성에 관한 연구
류수착,Ryu, Su-Chak 한국재료학회 1999 한국재료학회지 Vol.9 No.9
TiO$_2$분말을 $Al_2$O$_3$분말에 대하여 무게비로 1,3,5,7,9와 11wt%로 혼합하여 알루미나 세라믹스의 미세조직 및 기계적 물성변화를 관찰하였다. TiO$_2$분말의 첨가량이 증가할수록 부피비중은 3.26에서 2.90g/㎤으로 감소하였으며 기공율은 TiO$_2$분말의 첨가량이 7wt%까지는 감소하였으나 9wt%이상 첨가할 경우 증가하였다. 압축강도 측정 결과 파괴강도는 TiO$_2$분말의 첨가량이 7wt%까지는 증가하였으나 9wt%이상 첨가할 경우 감소하였다. 3점 곡강도를 측정한 결과 최대 파괴 응력 값은 TiO$_2$분말의 첨가량이 증가할수록 감소하였다. The effects of Tio$_2$addition on the microstructural evolution and mechanical properties of alumina ceramics were studied. Bulk density decreased with an increase of the amount of TiO$_2$. Apparent porosity decreased with an increase of the amount of TiO$_2$ up to 7wt%. But beyond 9wt% of TiO$_2$powders, apparent porosity increased. In the compression test, the modulus increased with an increase of the amount of TiO$_2$addition. In the three point bending test, the stress at yield decreased with an increase of the amount of TiO$_2$ addition. The addition. The addition of TiO$_2$ promoted the grain growth of alumina ceramics.
류수착,Ryu, Su-Chak 한국세라믹학회 2002 한국세라믹학회지 Vol.39 No.2
습식법에 의하여 제조된 $Al_2O_3$-1∼11 wt% $TiO_2$계 복합체를 1350$^{\circ}C$, 1450$^{\circ}C$ 에서 2시간 열처리 한 후 이에 대한 기계적 물성변화 및 미세구조를 조사하였다. 그 결과, $TiO_2$ 첨가량이 3 wt%였을 때의 복합체가 bulk density도 높고 기공율도 낮은 치밀한 미세구조를 이루었으며 이 때 young's modulus는 35.5 GPa, 곡강도값은 68.7 MPa로서 다른 $TiO_2$ 첨가량에 비하여 우수한 물성을 나타내었다. $TiO_2$ 첨가량이 증가할 수록 많은 양의 aluminium titanate의 합성으로 인해 열팽창 계수는 낮은 값을 나타내었다. $Al_2O_3$ composites powders with 1∼11 wt% $TiO_2$ were prepared by wet method and sintered at 1350$^{\circ}C$, 1450$^{\circ}C$ for 2h. Mechanical properties and microstructural evolution were investigated in this study. $Al_2O_3$-3 wt% $TiO_2$ composite were high bulk density of 2.37 g/$cm^3$ and low apparent porosity of 6.3%. The composites containing of 3 wt% $TiO_2$ showed moderately high bending strength of 68.9 MPa and the young's modulus of 35.5 MPa. The composites with increasing $TiO_2$ contents exhibit reduced thermal expansion coefficient due to the formation of $Al_2TiO_5$ phase.
치아 내 수산화아파타이트(HAp) 삽입 후 미세구조에 관한 연구
류수착,Ryu Su Chak 한국재료학회 2004 한국재료학회지 Vol.14 No.11
Hydroxyapatite powder was injected into thehole of teeth. The microstructure of teeth and HAp were observed after immersed in $9\%$ salin solution at $37^{\circ}C$ from 1month to 6 months. The junction morphology of hydroxyapatite and tooth was enhanced and particle size of hydroapatite was decreased with increasing time. The firm waxy body was found due to the hardening of hydroxyapatite fine powder resulting from the destruction of initial powder with swelling. It is suggested that the junction morphology of hydroxyapatite and tooth was observed due to the $Ca^{2+}$ ion shift of hydroxyapatite.
굴패각과 인산으로부터 수산화아파타이트 분말 합성에 관한 연구
류수착,엄지영,Ryu, Su-Chark,Eom, Ji-Young 한국재료학회 2002 한국재료학회지 Vol.12 No.9
Hydroxyapatite powders were prepared after heating at $1250^{\circ}C$ by the direct reaction using oyster shells and $H_3$$PO_4$. Properties of hydroxyapatite powders were investigated as XRF, XRD, DTA, FT-IR, SEM. Only hydroxyapatite was observed in XRD powders which was heated at $1250^{\circ}C$ for 2 hours and there was no remained CaO in that sample. And the results of FT-IR of sample was confirmed hydroxyapatite. Sample was agglomerated together, but needle shape morphology was observed in powders heated at $1250^{\circ}C$.
굴 껍질로부터 제조된 calcium phosphate 결정상에 관한 연구
류수착,Ryu, Su Chak 한국재료학회 2003 한국재료학회지 Vol.13 No.4
Calcium phosphate was prepared by chemical reaction formula using Oyster shells and $H_3$$PO_4$solutions. After added to 0.1 M∼0.9$ M H_3$$PO_4$ solution for oyster shell, prepared powders were investigated for heating properties and formation phase with heat treatment temperatures. As the results of XRD analysis of heated powders at $500^{\circ}C$∼$1200^{\circ}C$,$ CaCO_3$ phases were observed at the temperature of below 900 $^{\circ}C$ and in the condition of 0.1 M∼0.9 M $H_3$$PO_4$ solutions. However, $CaCO_3$, $CaPO_3$(OH) and $Ca_3$($PO_4$)$_2$ phases were appeared at the temperature range between $500∼900^{\circ}C$ and in the solution of 0.7 M to 0.9 M $H_3$$PO_4$. $Ca_{ 5}$($PO_4$)$_3$(OH) and CaO phases due to the decarbonation of oyster shells($CaCO_3$) were appeared at above $1000^{\circ}C$ and in the solution of below 0.5 M $H_3$X$PO_4$. However in the case of above 0.7 M $H_3$$H_4$ solutions, $Ca_{5}$ ($PO_4$)$_3$(OH) was decomposed into $Ca_3$($PO_4$)$_2$ at more higher 100$0^{\circ}C$. Thus $Ca_3$(X$Ca_4$)$_2$ phases were appeared at higher than 100$0^{\circ}C$.
굴 패각으로부터 제조된 수산화아파타이트 분말 특성에 관한 연구
류수착,김혜성,Ryu, Su-Chak,Kim, Hye-Sung 한국재료학회 2003 한국재료학회지 Vol.13 No.11
Hydroxyapatite powders were prepared by oyster shells and phosphoric acid. They were heat treated at the $1300^{\circ}C$ for 2 hrs. Only hydroxyapatite phases were observed by the XRD analysis. XRF confirmed that the prepared hydroxyapatite composed with 63.2wt% CaO and 35.7wt% $P_2$$O_{5}$ . In the ICP test, small amount of heavy metals were detected as low as 0.009 ppm Ti and 0.002 ppm Ba. The test of bone density was done in human body during three months. As the periods of medication progressed, the bone density was increased.