烷氧基衍生BaB2O4的形成与转化

O. Yamaguchi, K. Tominaga, K. Shimizu
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引用次数: 6

摘要

偏硼酸钡是由钡和硼醇氧化物同时水解而成。将所制备的BaB2O4脱水后的化合物称为γ-BaB2O4。γ-BaB2O4的IR模式可以归因于由(-BO2)−单元组成的链阴离子。在590 ~ 650℃和870 ~ 940℃分别观察到γ-转化为β-BaB2O4和β-转化为αBaB2O4。从高温x射线分析和DTA数据的结果来看,这两种转变都是不可逆的。γ-转变为β-BaB2O4的等温线由一阶方程描述,确定了γ-成核和扩展过程的活化能分别为69 kcal/mol和48 kcal/mol。β-转变为α-BaB2O4的动力学最好用收缩立方方程来解释。初始活化能为126 kcal/mol,最终活化能为76 kcal/mol。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formation and transformation of alkoxy-derived BaB2O4

Barium metaborate was formed by the simultaneous hydrolysis of barium and boron alkoxides. The dehydrated compound of the as-prepared BaB2O4 is termed γ-BaB2O4. The IR pattern of γ-BaB2O4 was able to be ascribed to a chain anion made up of (-BO2) units. The transformation of γ- into β-BaB2O4 and of β- into αBaB2O4 was observed at 590–650°C and 870–940°C, respectively. From the results of the high-temperature X-ray analysis as well as the DTA data, both transformations were found to be irreversible. Transformation isotherms of γ- into β-BaB2O4 were described by the first-order equation and activation energies were determined as 69 kcal/mol and 48 kcal/mol for nucleation process and propagation process, respectively. The kinetics of transformation of β- into α-BaB2O4 was best interpreted by the contracting cube equation. Activation energies were 126 kcal/mol and 76 kcal/mol for initial and final stages, respectively.

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