以溶胶凝胶法制备负热膨胀材料ZrW2O8粉体并与固相法制备的粉体相比较。对其前驱体进行热重-差热分析(TGDSC)、以X射线粉末衍射(XRD)、透射电镜(TEM)、扫描电子显微镜(SEM)分别对粉体进行物相分析和形貌观测。结果表明溶胶凝胶法比固相法合成温度低,于610℃合成单一立方结构ZrW2O8粉体,并且粉体颗粒比固相法小,为100nm;ZrW2O8粉体有很好的负热膨胀特性,以高温X射线衍射分析,在室温约500℃范围内,溶胶凝胶法制备的粉体的热膨胀系数为-5.93×10^-6/K;比固相法(-6.31×10^-6/K)的略低。
Negative thermal expansion material ZrW2O9 powders were synthesized using Sol-Gel chemistry method,and compared with powders which were synthesized using solid state reaction. The precursor of ZrW2O9 was studied by Thermogravimetric and differential scanning calorimetry (TG-DSC). The structure and morphology of the resulting powders were characterized by powder X-ray diffraction (XRD), Transmission electron microscopy(TEM) and scanning electron microscopy (SEM). The results showed that the temperature of the samples synthesized by sol-gel chemistry was lower than the powders prepared by solid state reaction,and the powders were single cubic phase of ZrW2O8 obtained at 610℃. The average dimension was smaller than powders synthesized by solid state reaction. The average size was 100nm. High temperature X-ray diffraction measurement indicated the powders had strong negative thermal expansion. The thermal expansion coefficient of ZrW2O8 synthe- sized by sol-gel chemistry was -5.93 × 10-6/K in the temperature range from room temperature to 500℃ ,and lower than which synthesized by solid state reaction(-6.31× 10^-6/K).