• Korean Journal of Materials Research
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• v.14 no.11
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• pp.786-789
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• 2004

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.

• Journal of the Korean Ceramic Society
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• v.45 no.10
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• pp.594-599
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• 2008

Hydroxyapatite(HA) was prepared from waste tuna bone, and its sintering property and dissolution behavior were investigated. Tuna bone derived-HA powder consisted of mainly HA and small amount of MgO. Porous HA ceramics with sintered density of 79% was obtained by pressureless sintering at $1200^{\circ}C$. Meanwhile, HA ceramics prepared by hot pressing at $1000^{\circ}C$ showed dense microstructure with sintered density of 95%. Immersion test revealed that both porous and dense HA ceramics were stable in liquid environment without distinct evidence of surface dissolution. It may be assumed that the presence of Mg in tuna bone-derived HA may improve dissolution resistance of HA.

• Journal of the Korean Ceramic Society
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• v.42 no.10 s.281
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• pp.660-664
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• 2005

Hydroxyapatite powder was injected into the tooth after decayed tooth clinic. The microstructure of tooth was observed after a tooth extraction in the body. The hydroxyapatite powder was stiffened and the junction of hydroxyapatite powder and tooth was observed. The Ca/P atomic ratio of hydroxyapatite-tooth boundary was higher than hydroxyapatite matrix. And microhardness of hydroxyapatite matrix was 92.4 Hv. The junction of hydroxyapatite powder and tooth was due to the $Ca^{2+}$ ion shift of hydroxyapatite or the firm waxy body was due to setting of hydroxyapatite powder.

• Proceedings of the Materials Research Society of Korea Conference
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• 2010.05a
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• pp.5.2-5.2
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• 2010

인체 경조직인 뼈와 치아는 콜라겐 단백질과 인산칼슘 무기질 성분으로 구성된 최적의 복합체라 볼 수 있다. 이러한 인산칼슘 무기질 성분은 결정학적, 화학적으로 hydroxyapatite (HA, Ca10(PO4)6(OH)2)와 거의 유사하여 높은 생체활성과 골전도성을 보이는 것으로 알려져 있다. 또한, hydroxyapatite의 고온 분해 산물로 볼 수 있는 tricalcuim phosphate(TCP, Ca3(PO4)2)는 체내에 이식시 체액에 용해되어 신생골을 유도하는 생체흡수성 세라믹스로 알려져있다. 이러한 HA와 TCP는 우수한 생체친화성에도 불구하고 기계적 특성이 낮아, non-load bearing 부위에 적용이 되어 다공질의 골수복재 용도로 활용되거나, load-bearing부위의 적용을 위한 금속 implant 등의 생체친화성 보완을 위한 표면 코팅재로 사용되고 있는 실정이다. 본 발표에서는 생체특성이 매우 우수한 인산칼슘 생체세라믹스의 load-bearing part 적용을 위하여 강도 및 파괴인성의 기계적 특성을 증진시킨 사례를 살펴보고, non-load bearing part에 실제 사용되는 인산칼슘 생체세라믹스의 다공질(porous) 골수복재(bone graft)의 역학 특성 증진을 위한 아이디어와 함께, 역학 특성이 매우 뛰어난 지르코니아 생체세라믹스의 강화-소결법에 대하여 소개하고자 한다.

• Korean Journal of Materials Research
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• v.16 no.4
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• pp.272-275
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• 2006

In order to evaluate the possibility of Polymethyl methacrylate (PMMA) as a binder on hydroxyapatite (HAp) which has good biocompatibility, the properties of HAp compacts with PMMA were examined. When adding 50 wt% of PMMA on HAp and pressed, the compression strength and the hardness of the compacting body were 168MPa and 55 Hv, respectively, and the strength of compacts was higher than that of cortical bone and the hardness was similar to the value of molar. We demonstrated that HAp ceramics can be obtained without additional heat treatment and machining of the ceramic was feasible. Therefore, the HAp compacts have potential to apply to implant or artificial bone after the clinical trials guarantees biocompatibility of it.

• Korean Journal of Materials Research
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• v.12 no.9
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• pp.747-749
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• 2002

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 $1250^{\circ}C$.

• Proceedings of the Korean Environmental Sciences Society Conference
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• 2008.11a
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• pp.423-427
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• 2008

지하수 중에 함유된 불소이온을 제거하기 위한 흡착제로 상용의 음이온교환수지(PA), 란탄산화물(La) 및 수산화아파타이트(HAp)를 선정하고 각각의 흡착특성을 회분식 실험을 통해 검토하였다. 그 결과를 요약하면 다음과 같다. 1) PA, La 및 HAp의 불소흡착은 Fruendlich isodtherm model 및 Pseudo-second-order kinetics model과 일치하는 거동을 보였다. 2) D-R model로부터 구한 흡착에너지는 9.66$\sim$12.90 kJ/mol로 이온교환메커니즘을 나타내는 흡착에너지 6$\sim$16 kJ/mol의 범위에 속하였다. 3) Van't Hoff 식에 이용하여 구한 ${\Delta}H^{\circ}$ 및 ${\Delta}G^{\circ}$값은 각각 3.40$\sim$89.28 kJ/mol과 -12.26$\sim$-13.76 kJ/mol의 범위를 보여 모두 흡착과정이 발열반응이며 자발적으로 일어나는 조건임을 알 수 있었다. 4) PA는 pH 6$\sim$8인 중성영역에서 가장 높은 불소 제거율을 보였으며, La과 HAp는 산성영역으로 갈수록 불소 제거율이 증가하는 특성을 나타내었다. 5) 불소에 대한 흡착선택성은 La$\geq$HAp>PA 순으로 높았으며, La의 경우 불소를 제외한 모든 음이온에 대한 흡착능이 없을 정도로 불소에 대한 흡착 특이성을 보였다.

• Journal of the Korean Ceramic Society
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• v.36 no.10
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• pp.1087-1093
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• 1999

Bioglass which is one of the surface active bionmaterials has a good biocompatibility but a poor mechanical strength, In the present work therefore two types of fluoride-containing bioglasses were coated on an alumina to improve mechanical strength. Crystallization of the coating layer and the hydroxyapatite formation on the bioactive glass coatings in tris-buffer solution were studied. When bioactive glass coated alumina was heat-treated Na2CaSi3O8 crystal was formed on the layer at lower temperature while wollastonite(CaSIO3) was obtained at higher temperature. Hydroxyapatite forming rate on the coating layer with Na2CaSi3O8 crystal was delayed with SiO2 contents in glass composition. However the hydroxyapatite was developed in 20minutes regardless SiO2 contents when the coating layer crystallized into wollastonite. More amount of P3+ ions were leached out of the coating layer with wollastonite than that with Na2CaSi3O8 crystal while Na+ and Ca2+ ions were leached out more easily from the Na2CaSi3O8 crystal containing coating layer.

• Journal of the Korean Ceramic Society
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• v.36 no.12
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• pp.1342-1349
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• 1999

In order to improve the density and the mechanical strength without change in chemical composition the hardened pastes of hydroxyapatite cement were reinforced with powders and/or whiskers of hydroxyapatite. The powders behaved as a seed of hydroxyapatite formation rather than a filler while the whiskers were mrerly dispersed in matrix and capillary pores of the hardened bodies leading to increase in mechanical strength. But the increase in strength But the increase in strength was nnt enough owing to the lack of homogeneous dispersion of the fibers. The highest diametral tensile strength of 18.5 MPa was measured at the hardened hydroxyapatite body in which well-dispersed whisker phase formed uniformly during hydro-thermal curing of power-added and dry-formed hydroxyapatite cement.

• Journal of the Korean Ceramic Society
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• v.42 no.11 s.282
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• pp.770-776
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• 2005

Hardening and hydroxyapatite(HAp) formation behavior of the bioactive cements in the system of $CaO-SiO_{2}-P_{2}O_{5}$ glasses and the corresponding glass-ceramics were studied. DCPD (Dicalcium Phosphate Dihydrate: $CaHPO_4{\cdot}2H_2O$) and DCPA (Dicalcium Phosphate Anhydrous: $CaHPO_4$) were developed when the prepared glass and glass-ceramic powders were mixed with three different solutions. The DCPD and DCPA transformed to HAp when the cement was soaked in Simulated Body Fluid (SBF), and this HAp formation strongly depended on the releasing capacity of $Ca^{2+}$ ions from the cements. The glass-ceramic containing apatite showed fast setting, but no HAp formation was observed because no $Ca^{2+}$ ions were released from this glass-ceramics. The compressive strength of the cements increased with reaction time in SBF until all DCPD and DCPA transformed to HAp.