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(K_xNa_(1-x))_(0.94)Li_(0.06)NbO_3陶瓷的相变特性和压电性能
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作者 钮效鹍 郑增艳 《石家庄学院学报》 2009年第3期13-15,共3页
利用传统陶瓷烧结工艺制备了(KxNa1-x)0.94Li0.06NbO3无铅压电陶瓷,研究了该系列陶瓷的微观晶体结构和压电性能.结果表明,随着组分的变化室温下该系列陶瓷呈现出2个正交-四方相界,分别位于x=0.40和x=0.60附近;组分x的变化对陶瓷的压电... 利用传统陶瓷烧结工艺制备了(KxNa1-x)0.94Li0.06NbO3无铅压电陶瓷,研究了该系列陶瓷的微观晶体结构和压电性能.结果表明,随着组分的变化室温下该系列陶瓷呈现出2个正交-四方相界,分别位于x=0.40和x=0.60附近;组分x的变化对陶瓷的压电性能影响显著,其中x=0.45的(K0.45Na0.55)0.94Li0.06NbO3陶瓷表现出最优异的压电性能(d33=205 pC/N,kp=48.5%). 展开更多
关键词 无铅陶瓷 晶体结构相变 压电性能
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高压下的同步辐射能量色散粉末衍射 被引量:18
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作者 刘景 赵菁 +1 位作者 车荣钲 杨洋 《高压物理学报》 EI CAS CSCD 北大核心 2000年第4期247-252,共6页
同步辐射已经成为高压研究的一个非常理想的光源。在北京同步辐射装置 (BSRF)上、结合金刚石对顶砧超高压实验技术建立起来的能量色散X射线粉末衍射系统 ,已用于物质状态方程和结构相变的研究。介绍了能量色散衍射方法 ,以及同步辐射原... 同步辐射已经成为高压研究的一个非常理想的光源。在北京同步辐射装置 (BSRF)上、结合金刚石对顶砧超高压实验技术建立起来的能量色散X射线粉末衍射系统 ,已用于物质状态方程和结构相变的研究。介绍了能量色散衍射方法 ,以及同步辐射原位测试过程。 展开更多
关键词 高压 同步辐射 能量色散 X射线衍射 晶体结构相变 状态方程 角度标定 能量标定 压力测量
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Antiphase boundary-like structure in α′′ martensite of TC21 titanium alloy 被引量:2
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作者 许艳飞 刘会群 +2 位作者 易丹青 朱知寿 郑峰 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2012年第6期1366-1371,共6页
The morphology and formation mechanism of the substructure of martensite in TC21 alloy was investigated by XRD and TEM. The results showed that the martensitic transformation from β to α" occurs upon quenching afte... The morphology and formation mechanism of the substructure of martensite in TC21 alloy was investigated by XRD and TEM. The results showed that the martensitic transformation from β to α" occurs upon quenching after solution treatment between 960-1000 ℃. The antiphase boundary (APB)-like structure was observed clearly in the α" martensite plates. The APB-like contrasts exist along the (001) and (020) planes of α" martensite. This APB-like structure of α" martensite was identified as a kind of stacking fault with an APB-like morphology induced by martensitic transformation and not by order/disorder transition. During martensitic transformation, martensitic domains nucleate and grow, eventually encounter each other, resulting in the formation of the APBdike contrast. 展开更多
关键词 titanium alloy martensitic transformation antiphase boundary (APB) crystal structure
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Reversible phase transition of the 1:1 complex between 18-crown-6 and n-propylammonium triiodide
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作者 GE JiaZhen 《Science China Chemistry》 SCIE EI CAS 2012年第2期208-213,共6页
Solid-state structure of the crystalline 1:1 complex [C3H10N(18-crown-6)]+[I3] (1) between 18-crown-6 and n-propylammonium triiodide has been determined at 293 and 93 K, respectively, showing a change from monoc... Solid-state structure of the crystalline 1:1 complex [C3H10N(18-crown-6)]+[I3] (1) between 18-crown-6 and n-propylammonium triiodide has been determined at 293 and 93 K, respectively, showing a change from monoclinic P21/m to monoclinic P21/a. Crystal structural analysis shows that in addition to van der Waals' forces, conventional N-H..-O hydrogen bonds are the key interactions. Measurements of unit cell parameters versus temperature show that the values of one of the three axes and the crystal volume change abruptly and remarkably at 220 K, indicating a first-order phase transition. The lack of the mirror plane in the low temperature structure is the most important differences between the two structural forms. Dif- ferential scanning calorimetry (DSC) measurement confirms that I undergoes a reversible phase transition at about 220 K with a thermal hysteresis of 3.5 K. The relatively large latent heat makes 1 a good candidate for phase change materials. The phase transition is accompanied by an anomaly of dielectric constant during heating and cooling process near the phase transition temperature. 展开更多
关键词 phase transition dielectric constant phase change material crown ether crystal structure
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