• 한국재료학회지
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• 제22권8호
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• pp.397-402
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• 2012

Morphological control on hydroxyapatite crystals has attractive prospects in research to clarify the effects of crystal planes on biological performance. Hydrothermal processing is known as a typical type of processing for fabricating well-grown crystals with unique morphology. The purpose of the present study is to examine the feasibility of well-crystallized crystals with oriented structures through hydrothermal treatment of calcite. A single crystal of calcite was applied to hydrothermal treatment in a phosphate solution at $160^{\circ}C$. Rod-shaped hydroxyapatite crystals with micrometer-size were formed on the {100} face of calcite after treatment, while nanometer-sized hydroxyapatite crystals were formed on the (111). The hydroxyapatite crystals formed on each plane were not morphologically changed with increasing treatment periods. An oriented structure of rod-shaped hydroxyapatite was constructed after hydrothermal treatment of {100} planes on the calcite single, while such orientation was not observed on the (111) plane after the treatment. The layer of hydroxyapatite formed on the {100} plane was thicker than that of the (111) plane. The {100} plane of calcite shows a higher reactivity than that of the (111) plane, which results in rapid crystal growth of hydroxyapatite. The difference in the morphology of the formed hydroxyapatite was governed by the reactivity of each crystal plane exposed to the surrounding solution.

• 한국결정성장학회지
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• 제12권3호
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• pp.144-148
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• 2002

수산화아파타이트/티타늄 복합체를 스파크 플라즈마 소결(SPS) 장치를 이용하여 4층 경사 기능 재료 (FGM)로 제조하였다. 수산화아파타이트/티타늄 복합체의 최대 밀도와 이축 강도는 $1200^{\circ}C$에서 8분 동안의 SPS 조건에서 얻었다. 그러나, 수산화아파타이트는 $1100^{\circ}C$에서 사칼슘인산염(TetCP)으로 분해되었고, 티탄산칼숨 화합물 ($CaTiO_3$)이 형성되었다. 수산화아파타이트에 티타늄을 첨가하면 수산화아파타이트가 저온에서 쉽게 분해되었다.

• 한국세라믹학회지
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• 제36권12호
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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.

• 공업화학
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• 제8권6호
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• pp.1000-1005
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• 1997

참치 뼈로부터 추출한 hydroxyapatite[$Ca_{10}(PO_4)_6(OH)_2$]를 습식법으로 분쇄한 후 여러 온도로 고상반응시킨 세라믹 소결체의 특성을 고찰하였다. Hydroxyapatite소결체의 밀도는 $1350^{\circ}C$에서 약 $2.93g/cm^3$으로서 이론치의 $3.21g/cm^3$과 유사하였다. $1300^{\circ}C$ 이하의 소결온도에서는 hydroxyapatite가 결정상으로 나타났으며, 온도가 증가할수록 hydroxyapatite의 분해에 따른 whitlockite[$Ca_3(PO_4)_2$]의 결정상이 관찰되었다. 소결채의 미세구조는 발달된 입계들 사이에 폐기공들이 분포하였다. $1350^{\circ}C$의 소결시편 평균강도는 58MPa로 나타나 관절연골(articular cartilage)의 최대강도인 40MPa보다 우수한 것으로 나타났다.

• 공업화학
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• 제9권3호
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• pp.322-329
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• 1998

참치 뼈에서 추출한 hydroxyapatite를 출발물질로 여러 가지 세라믹 복합체를 제조하여 인공체액에서의 hydroxyapatite 복합체간의 화학결합을 조사하였다. Hydroxyapatite 복합체들은 인공체액에서 4주 후부터 화학 결합성질을 나타내었다. 결합강도는 bioglass가 가장 강하게 나타났으며, 조성에 따른 의존성은 관찰할 수 없었다. 인공체액에서 복합체들은 이들의 경계면에서 불균일 핵생성 및 성장에 의해 화학적 결합으로 이루어졌다.

• 한국세라믹학회지
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• 제38권12호
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• pp.1132-1136
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• 2001

생체친화성이 증진된 생체재료를 얻기 위하여 실리콘 원료로 tetraethyl orthosilicate를 사용하여 실리콘이 치환된 hydroxyapatite를 합성하였다. XRD 분석결과 규산이나 다른 인산칼슘염을 포함하지 않는 순수한 hydroxyapatite상 만이 존재하는 것을 확인할 수 있었다. 성분분석 결과 3.32wt% 까지의 실리콘을 함유하였다. $^{29}$ Si MAS NMR 데이터 분석결과 실리콘은 수산화아파타이트의 결정 내에서 규산염 사면체구조를 가지는 것으로 확인할 수 있었다. FT-IR 분석결과 Si 치환 수산화아파타이트에서 수산기가 감소되는 것은 silicate group의 음전하를 보상하기위한 것으로 사료되었다.

• The Korean Journal of Ceramics
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• 제5권2호
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• pp.162-164
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• 1999

Microsotructure designed porous ceramics of calcium hydroxyapatite $(Ca_{10}(PO_4)_6(OH)_2)$ were prepared by hydrothermal method. The particle size, shape, and the micro-pore size of the porous hydroxyapatite ceramics could becontrolled. The hydroxyapatite was non-stoichiometric apatite with calcium deficient compositions (Ca/P ratio < 1.67). The composition of non-stoichiometric hydroxyapatite ceramics could be controlled from 1.50 to 1.63 in Ca/P ratio. The hydroxyapatite ceramics preparedc at $105^{\circ}C$ under the saturated vapor pressure for 20h were composed of rod-shaped crystals with about 10$\mu\textrm{m}$ in length with the mean aspect ratio of 40. The porous ceramics of calcium deficient hydroxyapatite had about 45% porosity with the inter-connecting pore structure. Porous hydroxyapatite ceramics prepared hydrothermally had the compressive strength of about 10 to 30 MPa. In addition, porous ceramics of $\beta$-tricalcium phosphate ($\beta-Ca_3(PO_4)_2$) were prepared from the calcium deficient hydroxyapatite.

• 치위생과학회지
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• 제2권2호
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• pp.121-124
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• 2002

본 연구에서는 구강미생물에서 발견되는 FTF 효소의 hydroxyapatite에 대한 친화도와 상호간의 결합에 영향을 주는 요소들을 비교하였으며, hydroxyapatite에 결합된 FTF 효소의 효소활성은 매우 안정적으로 높은 효소활성을 보였다. 결과를 요약하면 다음과 같다. 1. FTF는 치아를 대신하여 사용한 hydroxyapatite의 표면상태와 표면적에 영향을 받는 것으로 나타났다. 2. Hydroxyapatite에 결합된 FTF는 높은 플락탄 생성능을 보여, 비결합 FTF와 비교시, 약 70%의 효소활성을 나타내었다. 3. 결합된 FTF는 비결합 FTF와 비교시, 단백질분해효소의 분해작용에 대한 높은 저항성을 보여, hydroxyapatite에 결합된 효소에서는 3차원적인 구조적 변화가 나타나는 것으로 판단된다.

• 한국결정성장학회지
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• 제24권5호
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• pp.219-223
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• 2014

Pulsed laser ablation in liquid medium was successfully employed to synthesize hydroxyapatite colloidal nanoparticles. The crystalline phase, particle morphology, size distribution and microstructure of the hydroxyapatite nanoparticles were investigated in detail. The obtained hydroxyapatite nanoparticles had spherical shape with sizes ranging from 5 to 20 nm. The laser ablation and the nanoparticle forming process were discussed with explosive ejection mechanism by investigating change of surface morphology on target. The analytical results of XPS, FT-IR and Raman spectroscopy confirms that the stoichiometry and bonding properties of the hydroxyapatite nanoparticles are in good agreement with reported bulk hydroxyapatite materials.

• 한국재료학회지
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• 제14권11호
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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.