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首页> 外文期刊>Journal of Materials Science >Selective localization of nanohydroxyapatite in poly(3-hydroxybutyrate)/polycaprolactone blends composites and its effects on crystallization and molecular dynamics
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Selective localization of nanohydroxyapatite in poly(3-hydroxybutyrate)/polycaprolactone blends composites and its effects on crystallization and molecular dynamics

机译:聚(3-羟基丁酯)/聚己内酯共混复合材料中纳米羟基磷灰石的选择性定位及其对结晶和分子动力学的影响

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摘要

This work deals with the thermodynamic selective localization of hydroxyapatite nanoparticles (Hap) and its effects on crystallization and molecular dynamics in immiscible polyester blend films based on poly(3-hydroxybutyrate) (PHB, 90 wt%) and polycaprolactone (PCL, 10 wt%). Polymer blend composite films were obtained through solution casting method and characterized by contact angle (surface energy measurements), ultraviolet-visible spectroscopy (UV-Vis), elemental mapping, X-ray diffraction (WAXD), differential scanning calorimetry (DSC), polarized optical microscopy (POM) and time domain nuclear magnetic resonance (TD-NMR) techniques. It was found that hydroxyapatite (Hap) is selectively localized in the PHB phase and consequently, nanoparticles strongly influenced the PHB crystallization behavior. DSC and POM results indicated that hydroxyapatite nanoparticles acted as a nucleating agent. However, no significant changes in crystallinity degree were observed by WAXD. Fractionated crystallization behavior was observed for PCL droplets and the increase in the Hap concentration promoted heterogeneous nucleation on the droplets surface due to the nanoparticles close to the interface. Molecular dynamics studies by TD-NMR suggested a disordered Hap nanoparticles distribution inside the polymer matrix, leading to slower dynamics in the semirigid fraction of the sample ' s magnetization, typically attributed to restricted polymeric chains close to the particle's surface.
机译:本文研究了羟基磷灰石纳米颗粒(Hap)的热力学选择性定位及其对基于聚3-羟基丁酸酯(PHB,90 wt%)和聚己内酯(PCL,10 wt%)的不互溶聚酯共混膜结晶和分子动力学的影响。采用溶液浇铸法制备了聚合物共混复合薄膜,并通过接触角(表面能测量)、紫外可见光谱(UV-Vis)、元素映射、X射线衍射(WAXD)、差示扫描量热法(DSC)、偏光显微镜(POM)和时域核磁共振(TD-NMR)技术对其进行了表征。研究发现,羟基磷灰石(Hap)选择性地定位于PHB相,因此,纳米粒子强烈影响PHB结晶行为。DSC和POM结果表明,羟基磷灰石纳米粒子起到了成核剂的作用。然而,WAXD没有观察到结晶度的显著变化。观察到PCL液滴的分馏结晶行为,由于纳米颗粒靠近界面,Hap浓度的增加促进了液滴表面的异相成核。通过TD-NMR进行的分子动力学研究表明,Hap纳米颗粒在聚合物基质中的无序分布,导致样品磁化的半刚性部分的动力学变慢,这通常归因于靠近颗粒表面的受限聚合物链。

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  • 来源
    《Journal of Materials Science》 |2021年第5期|共21页
  • 作者单位

    Univ Fed Rio de Janeiro Ctr Tecnol Inst Macromol Prof Eloisa Mano Av Horacio Macedo 2030 Bloco J BR-21941598 Rio De Janeiro RJ Brazil;

    Univ Fed Rio de Janeiro Ctr Tecnol Inst Macromol Prof Eloisa Mano Av Horacio Macedo 2030 Bloco J BR-21941598 Rio De Janeiro RJ Brazil;

    Univ Fed Rio de Janeiro Ctr Tecnol Inst Macromol Prof Eloisa Mano Av Horacio Macedo 2030 Bloco J BR-21941598 Rio De Janeiro RJ Brazil;

    Univ Fed Rio de Janeiro Ctr Tecnol Inst Macromol Prof Eloisa Mano Av Horacio Macedo 2030 Bloco J BR-21941598 Rio De Janeiro RJ Brazil;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 工程材料学;
  • 关键词

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