首页> 外文期刊>Cearmics >STRUCTURE AND CHARACTERIZATION OF SOME HIGH CHEMICALLY RESISTANCE SILICATE GLASSES
【24h】

STRUCTURE AND CHARACTERIZATION OF SOME HIGH CHEMICALLY RESISTANCE SILICATE GLASSES

机译:某些高耐化学硅酸盐玻璃的结构和表征

获取原文
获取外文期刊封面目录资料

摘要

A multi component silicate glasses based on Li?O-MgO-P?O?-SiO? system were synthesized and modified by Na?O /Li?O, SrO /MgO and CaO /SrO replacements. The prepared glasses have been characterized by X-ray Diffraction (XRD) and Fourier Transform Infrared Spectroscopy (FTIR). Additionally, bulk density, microhardness, chemical durability and in vitro bioactivity were evaluated as a function of introducing different alkali and alkaline element substitutions. For comprehension the in vitro bioactivity, the glass samples were soaking in simulated body fluid (SBF) solution at 37°C for 14 days. Scanning electron microscopy coupled with energy-dispersive X-ray (SEM-EDX) and (FTIR) were used to characterize forming hydroxyapatite layer produced on glass specimen surfaces. The results show that Na?O/Li?O and CaO/SrO replacements led to enhance the bioactivity behavior of the glasses. The results are harmonious with a weaker network glass structure consequence of Na?O/Li?O and SrO/MgO replacement in the glasses. However, the glass network connectivity increased with addition of the higher charge to size ratio of Ca~(2+) instead of Sr~(2+). The prepared glass samples had microhardness in the range, 4920-6017 MPa; density values in the range, 2.46-2.78 g/cm3 and the weight loss percent was ranged between 0.72 and 1.67 %.
机译:基于Li 2 O-MgO-P 2 O 3 -SiO 2的多组分硅酸盐玻璃。用Na2O / Li2O,SrO / MgO和CaO / SrO替代物合成和修饰了该系统。所制备的玻璃已经通过X射线衍射(XRD)和傅立叶变换红外光谱(FTIR)表征。另外,根据引入不同的碱和碱元素替代物来评估堆积密度,显微硬度,化学耐久性和体外生物活性。为了了解其体外生物活性,将玻璃样品在37°C的模拟体液(SBF)溶液中浸泡14天。扫描电子显微镜与能量色散X射线(SEM-EDX)和(FTIR)耦合用于表征在玻璃样品表面上形成的羟基磷灰石层。结果表明,Na 2 O / Li 2 O和CaO / SrO的替代导致增强了玻璃的生物活性。结果与玻璃中Na2O / Li2O和SrO / MgO替代的较弱网络玻璃结构的结果相协调。然而,玻璃网络的连通性随着Ca〜(2+)而不是Sr〜(2+)的更高的体积比而增加。制备的玻璃样品的显微硬度在4920-6017 MPa的范围内。密度值在2.46-2.78 g / cm3的范围内,重量损失百分比在0.72至1.67%的范围内。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号