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    題名: 聚乳酸薄膜及複合材之機械性質研究
    Mechanical properties of polylactide films and composites
    作者: 黃慧平
    Hwang Huey-Ping
    貢獻者: 口腔復健醫學研究所
    關鍵詞: 可吸收性複合材
    聚乳酸
    變形區
    氫氧磷灰石
    機械性質
    resorbable composite
    polylactide
    deformation zone
    hydroxyapatite
    mechanical properties
    日期: 1997
    上傳時間: 2009-09-10 16:15:41 (UTC+8)
    摘要: 聚乳酸是一種良好的骨接合固定裝置材料,它具有良好的生物相容性及機械性質,且在
    體內可被吸收代謝等優點,因此毋需進行二次移除手術;另一方面,一般合成不易得到超高
    分子量的聚乳酸,導致機械性質亦受影響,而無法適用於體內必須承受較大應力的骨折處,
    此為其臨床應用上的一大缺失.本研究中,先將聚乳酸製成薄膜,浸泡於磷酸緩衝溶液(PBS)
    中0,1,3週,再將各薄膜試樣進行拉伸試驗,觀察,分析拉伸過程所產生的變形區,以瞭解其
    破壞行為與活體外退化情況,作為改良聚乳酸機械性質的知識基礎;再以壓縮模具技術依不
    同加工條件將含0,10wt%,30wt%,50wt%氫氧磷灰石的聚乳酸製成40*4*3mm^3的塊狀試樣,進
    行機械性質,熱性質,分子量,斷面形態觀察等各項物理性質的探討.
    研究結果顯示聚乳酸薄膜的破壞行為屬於脆性破壞;而無論薄膜是否浸泡過PBS,並不
    影響本身的降伏強度,但未浸泡的薄膜具較差的機械穩定性;結晶薄膜與非結晶薄膜的降
    伏強度無明顯差異,但結晶薄膜變形區孕核首先發生在晶界間的非結晶區域.
    在複合材塊狀試樣部份,氫氧磷灰石含量愈高,彎曲強度愈小,彎曲模數愈高,所含聚
    乳酸之結晶度愈小,但複合材的玻璃轉化溫度與熔點則無顯著改變;含氫氧磷灰石比例相
    同時,氫氧磷灰石顆粒愈大者,彎曲模數愈小,所含聚乳酸之結晶度愈大,而複合材的玻璃
    轉化溫度與熔點亦無顯著改變;以掃瞄式電子顯微鏡觀察斷面形態,發現氫氧磷灰石/聚
    乳酸複合材為混合式斷裂,在高含量氫氧磷灰石試樣中,氫氧磷灰石與聚乳酸界面間存在
    有空隙,其結合性不佳,可能為機械性質降低的原因.
    Poly-L-lactide(PLLA)is an excellent osteosynthesis material because it has
    good biocompatibility and it can be metabolized completely in humam body. On
    the other hand, commercial PLLA with a high molecular weight, over 5*10^6, was
    difficult to make, resulting in limited mechanical properties and an
    insufficient application in stress-bearing fracture sites. In this study,
    first, PLLA film samples were made of commercial available PLLA, and immersed
    in phosphate buffer solution(PBS) for 0, 1, and 3 weeks. After stretching, the
    deformation zones of the film samples produced during the stretching process
    were observed and analyzed to investigate the micro-deformation behavior of
    PLLA. Then, PLLA reinforced with 0,10wt%,30wt%,50wt% hydroxyapatite(HA) was
    fabricated into a block(40*3*4 mm^3) using a compression molding technique
    under several processing conditions. The composite samples were tested by
    material testing system, differential scanning calorimetry and gel permeability
    chromatography, and the morphology of the fracture surfaces were observed by a
    scanning electronic microscope to investidate their physical properties.
    The results show that the PLLA film samples were deformed by crazing rather
    than shear. During 3 weeks, no matter whether the film samples immersed in PBS
    or not, the yield strength of the film samples was not affected. There were no
    significant differences between the yield strength of crystal and non-crystal
    film samples, but the nucleation of the deformation zone of the crystal film
    samples happened in the non-crystal areas first.
    The flexural strength and the crystallinity of PLLA composite samples
    decrease as the HA contents increased, while the Young''s modulus was reversed.
    When the HA contents are the same, the Young''s modulus decreased as the HA
    particle size became larger, while the crystallinity of PLLA in the samples
    was reversed. The morphology of the fracture surfaces of the samples shows
    that the fracture of HA/PLLA composites is a mix-type fracture, and the space
    between HA nad PLLA interface becomes larger as the HA contents increase. The
    decreasing bonding strength between HA and PLLA might be the reason for a
    decrease in flexural strength.
    資料類型: thesis
    顯示於類別:[牙醫學系] 博碩士論文

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