首页> 美国卫生研究院文献>Journal of Functional Biomaterials >Impact of Bi2O3 and ZrO2 Radiopacifiers on the Early Hydration and C–S–H Gel Structure of White Portland Cement
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Impact of Bi2O3 and ZrO2 Radiopacifiers on the Early Hydration and C–S–H Gel Structure of White Portland Cement

机译:Bi2O3和ZrO2辐射乳化剂对白色硅酸盐水泥的早期水化和C–S–H凝胶结构的影响

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摘要

Bismuth oxide (monoclinic α-Bi O ) and zirconium oxide (monoclinic ZrO ) are the most popular radiopacifiers in commercial Portland cement-based endodontic restoratives, yet their effects on the setting and hydration reactions are not fully understood. This study compares the impact of 20 wt.% of Bi O or ZrO on the early hydration reactions and C–S–H gel structure of white Portland cement (WPC). Cement paste samples were hydrated at 37.5 °C prior to analysis by Si and Al magic angle spinning nuclear magnetic resonance spectroscopy at 3 h and 24 h, and transmission electron microscopy at 3 h. Initial and final setting times were determined using a Vicat apparatus and reaction kinetics were monitored by isothermal conduction calorimetry. Bi O was found to prolong initial and final setting times and retard the degree of hydration by 32% at 24 h. Heat evolution during the acceleration and deceleration phases of the hydration process was reduced and the exotherm arising from renewed ettringite formation was delayed and diminished in the presence of Bi O . Conversely, ZrO had no significant impact on either setting time; although, it accelerated hydration by 23% within 24 h. Increases in the mean silicate chain length and the extent of aluminum substitution in the C–S–H gel were observed in the presence of both radiopacifying agents after 24 h relative to those of the unblended WPC. The Bi O and ZrO particles remained intact within the cement matrix and neither bismuth nor zirconium was chemically incorporated in the hydration products.
机译:氧化铋(单斜晶系的α-BiO)和氧化锆(单斜晶系的ZrO)是商用波特兰水泥基牙髓修复剂中最流行的射线不透性物质,但它们对凝结和水合反应的影响尚不完全清楚。这项研究比较了20 wt。%的Bi O或ZrO对白色波特兰水泥(WPC)的早期水合反应和C–S–H凝胶结构的影响。水泥浆样品在37.5°C下水化,然后在3 h和24 h进行Si和Al魔角旋转核磁共振波谱分析,并在3 h进行透射电子显微镜分析。使用Vicat仪器确定初始和最终凝固时间,并通过等温传导量热法监测反应动力学。发现Bi O会延长初始和最终凝固时间,并在24小时内将水合度延迟32%。在Bi O的存在下,水化过程的加速和减速阶段的放热减少了,由重新形成的钙矾石形成引起的放热得以延迟和减少。相反,ZrO对凝结时间均无显着影响。但是,它在24小时内将水合速度提高了23%。相对于未掺混的WPC,在两种辐射不透性剂存在下,在24小时后,在C–S–H凝胶中平均硅酸盐链长和铝取代程度的增加。 Bi O和ZrO颗粒在水泥基质中保持完整,并且铋和锆均未化学掺入水合产物中。

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