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A homogenous CS/NaCMC-HA polyelectrolyte complex membrane prepared by gradual electrostatic assembling

机译:通过逐步静电组装制备均质的CS / NaCMC / n-HA聚电解质复合膜

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摘要

A homogenous membrane composed of chitosan (CS), sodium carboxymethyl cellulose (NaCMC) and nano hydroxyapatite (n-HA) was prepared by a gradual electrostatic assembling (GEA) method. The physical and chemical properties of the membranes with different n-HA contents and CS/NaCMC ratios were characterized by Scanning electron microscopy, Fourier transform infrared spectros-copy, X-ray diffraction and mechanical test. The schematic formation mechanism of the membrane was discussed. The results show that GEA is an effective method to prepare the polyelectrolyte complex (PEC) membrane, in which oppositely charged CS-NaCMC polysaccharides can assemble mildly and gradually through electrostatic interaction to form the membrane framework, while the filled n-HA crystals can regulate the structure stability of the composite membrane. The optimum preparation condition for the PEC membrane can be fixed to a content of 60 wt% n-HA, an equivalent amount of CS to NaCMC and a drying temperature of 60°C. The PEC membrane may have good prospect for guided bone regeneration.
机译:通过逐步静电组装(GEA)方法制备了由壳聚糖(CS),羧甲基纤维素钠(NaCMC)和纳米羟基磷灰石(n-HA)组成的均质膜。通过扫描电子显微镜,傅里叶变换红外光谱,X射线衍射和力学性能测试,表征了不同n-HA含量和CS / NaCMC比的膜的理化性质。讨论了膜的示意性形成机理。结果表明,GEA是制备聚电解质复合物(PEC)膜的有效方法,其中带相反电荷的CS-NaCMC多糖可以通过静电相互作用缓慢且逐渐地组装以形成膜骨架,而填充的n-HA晶体可以调节复合膜的结构稳定性。 PEC膜的最佳制备条件可以固定为n-HA的含量为60wt%,CS与NaCMC的当量以及干燥温度为60°C。 PEC膜可能具有引导骨再生的良好前景。

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  • 来源
    《Journal of materials science》 |2011年第2期|p.289-297|共9页
  • 作者单位

    Research Center for Nano Biomaterials, Analytical and Testing Center, Sichuan University, Chengdu 610064, People's Republic of China;

    Research Center for Nano Biomaterials, Analytical and Testing Center, Sichuan University, Chengdu 610064, People's Republic of China;

    Research Center for Nano Biomaterials, Analytical and Testing Center, Sichuan University, Chengdu 610064, People's Republic of China;

    Research Center for Nano Biomaterials, Analytical and Testing Center, Sichuan University, Chengdu 610064, People's Republic of China;

    Research Center for Nano Biomaterials, Analytical and Testing Center, Sichuan University, Chengdu 610064, People's Republic of China;

    Research Center for Nano Biomaterials, Analytical and Testing Center, Sichuan University, Chengdu 610064, People's Republic of China;

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