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Preparation and Characterization of Ultra-Fine ZrB_2 Powders from Inorganic-Organic Hybrid Precursors via Carbothermal Reduction

机译:通过Carbothotmal降低制备来自无机 - 有机杂交前体的超细ZrB_2粉末的制备和表征

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Ultra-fme zirconium diboride powders were synthesized by using inorganic-organic hybrid precursors of zirconium (IV) nitrate pentahydrate, boric acid and citric acid as sources of zirconia, boron oxide and carbon, respectively. The effect of molar ratio of reactants and reaction temperatures on the as-synthesized precursors were investigated. The thermodynamic change in the ZrO_2-B_2O_3-C system was studied by thermogravimetric and differential scanning calorimetry. The phase compositions and crystalline state of the products after heat treatment was determined by XRD and the crystallite size and morphology of the synthesized powders were characterized by SEM. It was found that the as-synthesized precursor with B/Zr molar ratio of 3.5 can transform into ZrB_2 and ZrC by heating in an argon atmosphere with temperatures as low as 1400°C and the synthesized powders exhibited near-spherical morphology with a samll average crystallite size of about 200 mn and dispersed relatively uniformly. Moreover, with the reaction temperature increased, the purity of the zirconium diboride powders are higher. The mixture was finally transformed into pure zirconium diboride at 1600°C. However,the grain sizes increased significantly and tended to be aggregated with the reaction temperature increased to 1600°C. The synthesized ZrB_2 powders showed a porous structure and the grain sizes on the exterior is larger than the interior because of the higher heat treatment temperature.The finally single ultra-fme ZrB_2 grain sizes weredistributed from 190nm to 690nm in two-dimensions and have a larger specific surface area of88.14m~2/g.
机译:通过使用锆(IV)硝酸盐五水合物,硼酸和柠檬酸作为氧化锆,氧化硼和碳的根源,合成超FME锆二硼胺粉末。研究了反应物和反应温度对粘合剂的摩尔比的影响。通过热重分析和差示扫描量热法研究了ZrO_2-B_2O_3-C系统的热力学变化。通过XRD测定热处理后产物的相组合物和结晶状态,通过SEM表征合成粉末的微晶尺寸和形态。发现具有3.5的B / ZR摩尔比的AS合成的前体可以通过在氩气氛中加热至低至1400℃的温度,并且合成的粉末具有近球形形态,具有SAMLL平均值的近似球形形态转化为ZRB_2和Zrc。微晶尺寸约为200mN并相对均匀地分散。此外,随着反应温度的增加,锆二硼化锆粉末的纯度较高。最终将混合物在1600℃下转化为纯锆二硼化物。然而,晶粒尺寸显着增加并且倾向于与反应温度增加到1600℃的聚集。合成的ZrB_2粉末显示出多孔结构,外部上的晶粒尺寸大于内部,因为较高的热处理温度。最后单个超FME Zrb_2粒度从190nm到690nm中的两个维度呈现,并且具有更大的比表面积为88.14m〜2 / g。

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