請用此 Handle URI 來引用此文件:
http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/23229完整後設資料紀錄
| DC 欄位 | 值 | 語言 |
|---|---|---|
| dc.contributor.advisor | 李源弘 | |
| dc.contributor.author | Jui-Yi Lin | en |
| dc.contributor.author | 林瑞益 | zh_TW |
| dc.date.accessioned | 2021-06-08T04:48:39Z | - |
| dc.date.copyright | 2009-07-31 | |
| dc.date.issued | 2009 | |
| dc.date.submitted | 2009-07-28 | |
| dc.identifier.citation | [1] L.L Hench, J. Wilson, “An introduction to bioceramics”, World Scientific Publishing Co. Pte. Ltd. (1993).
[2]L.L Hench, E.C Ethridge “Biomaterial”, Academic Press. Inc. (1982) [3]洪敏雄,林峰輝,王盈錦,“生醫陶瓷”,陶瓷技術手冊(下),中華民國產業科技發展協進會(1994)。 [4]G. Daculsi, “Biotechnology for calcium phosphate bioactive ceramics in bone repair” The Chinese Society for Materials, Annual Meeting Workshop (1999). [5] C.S.B. Ben-Nissan, “Bioactive nanocrystalline sol-gel hydroxyapatite coating” Journal of Material Science: Materials in Medicine 10 (1999) 465-469. [6]J.E. Lemons, “Hydroxyapatite coatings” Clinical Orthopaedics and Related Research 235 (1998) 220-223. [7]K.A. Thomas, J.F .Kay, S. D. Cook, M. Jarcho, “The effect of surface macrotexture and hydroxyapatite coating on the mechanical strength and histologic profiles of titanium implant materials” Journal of Biomedical Materials Research 21 (1987) 1395-1414. [8]D. Buser, R.K. Schenk, S.Steinemann, J.P. Fiorellini, C.H. Fox, H. Stich, “Influence of surface characteristics on bone intergration of titanium implants. A histomorphometric study in miniature pigs” Journal of Biomedical Materials Research 25 (1991) 889-902. [9]J.A. Jansen, J.P.C. M. van de Waerden, G.C. Wolke, K.De Groot, “Histologic evaluation of the osseous adaptation to titanium and hydroy-apatite-coated titanium implants“ Journal of Biomedical Materials Research 25 (1991) 973-989. [10]M. Jarcho, C.H. Bolen, M.B. Thomas, J. Bobick, J.F. Kay, R.H. Doremus, “Hydroxyapatite synthesis and characterization in dense polycrystalline form” Journal of Materials Science 11 (1976) 2027-2035. [11]S.F. Hulbert, J.J. Klawitter, L.S. Bowman, “History of ceramic orthopedic implants” Materials Research Bulletin 7 (1972) 1239-1246. [12]M.I. Kay, R.A. Young, A.S. Posner, “Crystal structure of hydroxyapatite” Nature 204 (1964) 1050-1052. [13]K. de Groot, “Bioceramics of calcium phosphate”, CRC Press. Inc., Boca Raton, Florida, (1983) 1-32 79-97. [14]R.Z Legeros, “Calcium phosphates in oral biology and medicine” Monographs in Oral Sciences 15 (1991) 151-201. [15]W. Suchanek, M.Yoshimura, “Processing and properties of hydroxyapatite-based biomaterials for use as hard tissue replacement implants” Journal of Materials Research 13 (1998) 94-117. [16]T. Kijima, M. Tsutsumi, “Preparation and thermal properties of dense polycrystalline oxyhydroxyapatite” Journal of the American Ceramic Society 62 (1979) 455-460. [17]G. Willmann, “Medical grade hydroxyapatite: state of the art” British Ceramic Transactions 95 (1995) 212-216. [18]F.C.M. Driessens, “Bioceramic of Calcium Phosphate” Edited by K. de Groot, CRC Press Inc., Boca Raton, Florida (1983) 1-32. [19]P. Adam, A. Nebelung, M. Vogt, “Verhalten von mit tricalcium phosphate schichteten titanimplantion bei der behandlung mit wasser von 80℃ (Behavior of titantium implants coated with tricalcium phosphate during treatment with water at 80℃)” Sprechsaal (1988) 941-944. [20]H. Newesely, “High temperature behavior of hydroxyl- and fluorapatite” Journal of Oral Rehabilitation 4 (1977) 97-104. [21]W.E. Brown, L.C. Chow, “Thermodynamics of apatite crystal growth and dissolution” Journal of Crystal Growth 53 (1981) 31-41. [22]J.M. Burnell, E.J. Teubner, A.G. Miller, “Normal maturational changes in bone matrix, mineral, and crystal size in the rat” Calcified Tissue International 31 (1980) 13-19. [23]M.E.J. Curzon, F.J. Gil, M.P. Ginebra, “Calcium phosphate bonecements for clinical applications. Part I: solution chemistry” Journal of Material Science, Material in medicine 10 (1999) 167-176. [24]C.C. Berndt, G.N. Haddad, A.J.D. Farmer, K/ A. Gross, “Thermal spraying for bioceramic applications” Material Forum 14 (1990) 161-173. [25]汪建民,陶瓷技術手冊(上)、(下),中華民國粉末冶金學會,(1994)。 [26]張淑真,“水熱法合成氫氧基磷灰石之研究”,中原大學化學所碩士論文,(1993)。 [27]S. Pramanik, A.K. Agarwal, K.N. Rai, A. Garg, “Development of high strength hydroxyapatite by solid-state-sintering process” Ceramics International 33 (2007) 419–426. [28]謝維倫,“氫氧基磷灰石陶瓷厚膜之製備及其相關特性之研究”,義守大學材料工程與科學研究所碩士論文,(2002)。 [29]C. Liu, Y. Huan, W. Shen, J. Cui, “Kinetics of hydroxyapatite precipitation at pH10 to 11” Biomaterials 22 (2001) 301-306. [30]L. Bernard, M. Freche, J.L. Lacout, B. Biscans, “Preparation of hydroxyapatite by neutralization at low temperature-influence of purity of the raw material” Powder Technology 103 (1999) 19-25. [31]E.M. Rivera, M. Araiza, W. Brostow, V.M. Castaoo, J.R. Diaz-Estrada. R. Hernandez, J.R. Rodriguez, “Synthesis of hydroxyapatite from eggshells” Materials Letters 41 (1999) 128-134. [32]G.K. Lim, J. Wang, S.C. Ng, L.M. Gan, “Processing of fine hydroxyapatite powders via an inverse microemulsion route” Materials Letters 28 (1996) 431-436. [33]H.E. Lundager Madsen, F. Christensson, L.E. Polyak, E.I. Suvorova, M.O. Kliya, A.A. Chernov, “Calcium phosphate crystallization under terrestrial and microgravity conditions” Journal of Crystal Growth 152 (1995) 191-202. [34]Y. Fang, D.K. Agrawal, D.M. Roy, P.W. Brown, “Ultrasonically accelerated synthesis of hydroxyapatite” Journal of Materials Research 7 (1992) 2294-2298. [35]X. Sun, C. Ma, Y. Wang, H. Li, “Effects of polarization of calcium phosphate” Materials Letters 47 (2001) 267-270. [36]I. Mobasherpour, M.S. Heshajin, A. Kazemzadeh, M. Zakeri, “Synthesis of nanocrystalline hydroxyapatite by using precipitation method” Journal of Alloys and Compounds 430 (2007) 330-333. [37]W. Eysel, D.M. Roy, “Hydrothermal flux growth of hydroxyapatite by temperature oscillation” Journal of Crystal Growth 20 (1973) 245-250. [38]A. Jillavenkatesa, R. A. Condrate SR, “Sol-gel processing of hydroxyapatite” Journal of material science 33 (1998) 4111-4119. [39]R. Zhu, R. Yu, J. Yao, D. Wang , J. Ke, “Morphology control of hydroxyapatite through hydrothermal process” Journal of Alloys and Compounds 457 (2008) 555-559. [40]S. Ogo, A. Onda, K. Yanagisawa, “Hydrothermal synthesis of vanadate- substituted hydroxyapatites, and catalytic properties for conversion of 2-propanol” Applied Catalysis A: General 348 (2008) 129-134. [41]H. Anmin, L. Ming, C.C. Kang, M. Dali, “Preparation and characterization of titanium-substituted hydroxyapatite photocatalyst” Journal of Molecular Catalysis A: chemical 267 (2007) 79-85. [42]F. Zhang, Z.H. Zhou, S.P. Yang, L.H. Mao, H.M. Chen , X.B Yu, “Hydrothermal synthesis of hydroxyapatite nanorods in the presence of anionic starburst debdrimer” Materials Letters 59 (2005) 1422-1425. [43]J.D. Chen, Y.J. Wang, K. Wei, S.H. Zhang, X.T. Shi, “Self-organization of hydroxyapatite nanorods through oriented attachment” Biomaterials 28 (2007) 2275-2280. [44]M. Yoshimura, H. Suda, K. Okamoto, K. Ioku, “Hydrothermal synthesis of biocompatible whiskers” Journal of Materials Science 29 (1994) 3399-3402. [45]J. Liu, X. Ye, H. Wang, M. Zhu, B. Wang, H. Yan, “The influence of pH and temperature on the morphology of hydroxyapatite synthesized by hydrothermal method” Ceramics International 29 (2003) 629–633. [46]H.S. Liu, T.S .Chin, L.S. Lai, S.Y. Chiu, K.H. Chung, C.S. Chang , M.T. Lui, “Hydroxyapatite synthesized by a sinplified hydrothermal method” Ceramics International 23 (1997) 19-25. [47]J. Hu, J.J. Russeel, B. Ben-Nissan, “Production and analysis of hydroxyapatite from Australian corals via hydrothermal process” Journal of Materials Science Letters 20 (2001) 85– 87. [48]Y. Xu, D. Wang, L. Yang, H. Tang, “Hydrothermal conversion of coral into hydroxyapatite” Materials Characterization 47 (2001) 83– 87. [49]M. Yoshimura, P. Sujaridworakun, F.K.T. Fujiwara, D. Pongkao, A. Ahniyaz, “Hydrothermal conversion of calcite crystals to hydroxyapatite” Materials Science and Engineering C 24 (2004) 521-525. [50]X. Zhang , K.S. Vecchio, “Hydrothermal synthesis of hydroxyapatite rods” Journal of Crystal Growth 308 (2007) 133-140. [51]P. Sujaridworakun, F. Koh, T. Fujiwara, D. Pongkao, A. Ahniyaz, M. Yoshimura, “Preparation of anatase nanocrystals deposited on hydroxyapatite by hydrothermal treatment” Materials Science and Engineering C 25 (2005) 87-91. [52]L.C. Bonar, A. H. Roufosse, W. K. Sabine, M. D. Grynpas, M. J. Glimcher, “X-ray diffraction studies of the crystallinity of bone mineral in newly synthesized and density fractionated bone” Cacified Tissue International 35 (1983) 202-209. [53]A. Bartsiokas, A. P. Middleton, “Characterization and dating of recent and fossil bone by X-ray diffraction” Journal of Archaeological Science 19 (1992) 63-72. [54]A. Person, “Early diagenetic evolution of bone phosphate: an X-ray” Journal of Archaeological Science 22 (1995) 211-221. | |
| dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/23229 | - |
| dc.description.abstract | 本研究是利用水熱法來製備氫氧基磷灰石(Ca10(PO4)6(OH)2,HAp),將含有鈣離子(奈米碳酸鈣)及磷離子(磷酸二氫銨)之水溶液,與醋酸或氨水調整pH值後混合於密封壓力釜中,在不同水熱處理下控制長晶條件,形成高結晶性氫氧基磷灰石粉末。實驗結果發現,藉由XRD結果及計算其結晶性質,在pH=6、250℃、96小時之水熱條件下反應後,可達到結晶性最佳的HAp,以及一些殘留的β-磷酸三鈣(β-Ca3(PO4)2,β-TCP),所以HAp比較容易在水熱法酸性環境中形成。藉由FT-IR可判斷合成HAp的官能基,在pH=6、250℃、96小時所合成的HAp,其OH-和PO43-的吸收峰強度比pH=8和pH=10來的高。由EDX的結果得知於pH=6的條件下最接近HAp之Ca/P化學計量比1.67。由SEM及TEM結果得知HAp為柱狀,長度大約在18μm左右,其結構是屬於六方晶結構。由反應機制推斷,本研究中的HAp是藉由鈣離子溶解到水溶液中成核成長,以及藉由碳酸鈣先形成β-TCP,然後在β-TCP表面反應生成HAp,當pH=6、反應溫度250℃、反應時間為96小時,大部分的β-TCP都會形成HAp,只有少量的β-TCP殘留。 | zh_TW |
| dc.description.abstract | Hydroxyapatite (Ca10(PO4)6(OH)2, HAp) was synthesized by hydrothermal treatment. Nano calcium carbonate (CaCO3) was used as calcium source and diammonium hydrogen phosphate ((NH4)2HPO4) as phosphorous source. The pH value of solution was adjusted by CH3COOH or NH4OH, and then put solution in autoclave under different situation. After hydrothermal reaction finished, the well-crystallized HAp and a small amount of β-TCP were obtained. From FT-IR spectra, we can found that under pH=6, 250℃, 96hr, the functional group of OH- and PO43-, are stronger than pH=8 and pH=10, which suggests that at pH=6, the synthesized powder has more HAp phase than pH=8 and pH=10. From SEM and TEM pictures, HAp shows rod-like shape with length about 18μm and width about 1μm. The structure of HAp is HCP structure. From the reaction growth mechanism, the nucleation and growth of β-tricalcium phosphate (β-TCP) on the surface of calcite particle was observed at the beginning of the reaction of calcite. Some HAp rods were grown by β-TCP convert into HAp. Some HAp rods were grown by heterogeneous nucleation in the solution. After the hydrothermal reaction under pH=6, 250℃ for 96hr, most products are HAp with a small amount of β-TCP synthesized as a byproduct. | en |
| dc.description.provenance | Made available in DSpace on 2021-06-08T04:48:39Z (GMT). No. of bitstreams: 1 ntu-98-R94527003-1.pdf: 25886305 bytes, checksum: fe92df3a5753845b0901200dd69cdd8f (MD5) Previous issue date: 2009 | en |
| dc.description.tableofcontents | 口試委員會審定書.......................................... i
誌謝..................................................... ii 中文摘要................................................ iii 英文摘要................................................. iv 目錄.......................................................v 圖目錄..................................................viii 表目錄................................................. xiii 第一章緒論.................................................1 1-1 前言.................................................. 1 1-2 研究目的.............................................. 2 第二章理論基礎與文獻回顧.................................. 4 2-1生醫材料............................................... 4 2-1-1 生醫材料簡介........................................ 4 2-1-2 生醫陶瓷的應用...................................... 4 2-2 氫氧基磷灰石 ......................................... 7 2-3 氫氧基磷灰石的結構 ................................... 7 2-4 氫氧基磷灰石性質...................................... 9 2-4-1 氫氧基磷灰石物理與化學性質.......................... 9 2-4-2 氫氧基磷灰石室溫溶解度 ............................ 12 2-5 氫氧基磷灰石的合成 .................................. 15 2-5-1 固相反應法......................................... 16 2-5-2 化學共沉法...................................... 17 2-5-3 助熔劑法........................................... 19 2-5-4 溶膠凝膠法......................................... 20 2-5-5 水熱法 ............................................ 21 2-6 氫氧基磷灰石結晶性質的計算............................39 第三章實驗方法與步驟.................................... 41 3-1 實驗儀器與設備 ...................................... 41 3-2 實驗藥品 ............................................ 42 3-3 實驗方法 ............................................ 42 3-3-1 水熱法合成HAp之製備 ............................... 42 3-3-2 氫氧基磷灰石粉末分析方法 ......................... 44 3-3-2-1 X-ray繞射分析.................................... 44 3-3-2-2 掃瞄式電子顯微鏡分析............................. 44 3-3-2-3 穿透式電子顯微鏡分析............................. 44 3-3-2-4 傅利葉紅外線光譜儀分析........................... 44 第四章結果與討論 ........................................ 46 4-1 反應物分析........................................... 46 4-2 XRD繞射分析 ......................................... 50 4-2-1 pH=6 系統 ......................................... 50 4-2-2 pH=8 系統 ......................................... 54 4-2-3 pH=10 系統......................................... 56 4-2-4 XRD結論 ........................................... 58 4-3 掃描式電子顯微鏡分析 ................................ 59 4-3-1 pH=6 系統 ........................................ 59 4-3-2 pH=8 系統 ........................................ 68 4-3-3 pH=10 系統........................................ 77 4-3-4 SEM結論 .......................................... 86 4-4 穿透式電子顯微鏡分析................................. 87 4-5 HAp成份分析 ........................................ 93 4-5-1 傅利葉紅外線光譜儀分析(FT-IR)..................... 93 4-5-2 EDS分析.......................................... 94 4-6 結晶性質計算 ........................................ 95 4-7 反應機制探討......................................... 99 第五章 結論 .............................................100 參考文獻................................................ 101 | |
| dc.language.iso | zh-TW | |
| dc.subject | 氫氧基磷灰石(HAp) | zh_TW |
| dc.subject | β-TCP | zh_TW |
| dc.subject | 水熱法 | zh_TW |
| dc.subject | 奈米碳酸鈣 | zh_TW |
| dc.subject | Hydroxyapatite (HAp) | en |
| dc.subject | Hydrothermal | en |
| dc.subject | β-TCP | en |
| dc.subject | Nano calcium carbonate (CaCO3) | en |
| dc.title | 水熱法奈米碳酸鈣合成氫氧基磷灰石研究 | zh_TW |
| dc.title | Study on the Hydroxyapatite from Nanosized Calcium
Carbonate through Hydrothermal Method | en |
| dc.type | Thesis | |
| dc.date.schoolyear | 97-2 | |
| dc.description.degree | 碩士 | |
| dc.contributor.coadvisor | 吳玉祥 | |
| dc.contributor.oralexamcommittee | 張文固,陳軍華,劉典謨 | |
| dc.subject.keyword | 水熱法,氫氧基磷灰石(HAp),奈米碳酸鈣,β-TCP, | zh_TW |
| dc.subject.keyword | Hydrothermal,Hydroxyapatite (HAp),Nano calcium carbonate (CaCO3),β-TCP, | en |
| dc.relation.page | 106 | |
| dc.rights.note | 未授權 | |
| dc.date.accepted | 2009-07-29 | |
| dc.contributor.author-college | 工學院 | zh_TW |
| dc.contributor.author-dept | 材料科學與工程學研究所 | zh_TW |
| 顯示於系所單位: | 材料科學與工程學系 | |
文件中的檔案:
| 檔案 | 大小 | 格式 | |
|---|---|---|---|
| ntu-98-1.pdf 未授權公開取用 | 25.28 MB | Adobe PDF |
系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。
