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Auto ignition processing and hot isostatic pressing of nanocrystalline zirconia.

机译:纳米晶氧化锆的自动点火处理和热等静压。

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摘要

Two zirconia systems, CeO2-ZrO2 and CaO-ZrO2, are investigated in the current dissertation.; In the current study, Auto Ignition Process was successfully utilized in synthesizing nanocrystalline ZrO2 containing 2, 4, 6, 8, and 10mol% CaO and ZrO2 containing 4, 8, 12, 16, and 20mol% CeO 2. XRD, TEM, and Raman spectroscopy are used to characterize the as-synthesized powders. For both systems, the as-produced powders are tetragonal and the crystal sizes are less than 50nm. The crystalline size obtained decrease with increasing of CaO/CeO2 content. For CaO-ZrO2 system, the dominant defect in the produced ZrO2 is Cazr ″ and Vo··. The oxygen vacancy sits in the nearest-neighbor sites to Ca2+. The coordination number of Ca2+ is 7. For CeO2-ZrO2 system, neither Ce2O3, nor significant oxygen vacancy existed in the powders produced. The coordination number of Ce4+ in ZrO2 is 8. Vegard's law is obeyed in the current investigation of CeO2-ZrO2 system.; In the current study, as-synthesized ZrO2-6, 8, and 10mol% CaO and ZrO2-12, 16, and 20mol% CeO2 powders are successfully densified with retained nanocrystalline size and tetragonal structure using Hot Isostatic Pressing (HIPing). The mechanical properties testing found that hardness increases and fracture toughness decreases with CaO/CeO2 content in the above compositions. The hardness and fracture toughness of nanocrystalline zirconia are lower than those values of coarse grain zirconia. For ZrO2-6mol% CaO, the hardness obtained is 3.8GPa and the fracture toughness obtained is 4.10MPa.m1/2. For ZrO2-12mol% CeO2, the hardness obtained is 2.9GPa and the fracture toughness obtained is 5.18MPa.m1/2. These properties obtained can be explained by grain boundary sliding and absence of transformation toughening. A HIPing model developed in the current study indicates that diffusions is favored over power-law creep in the initial stage of HIPing and grain boundary diffusion is favored over lattice diffusion in the final stage of HIPing of nanocrystalline zirconia.
机译:本文研究了两种氧化锆体系,CeO2-ZrO2和CaO-ZrO2。在当前的研究中,自动点火过程已成功用于合成包含2、4、6、8和10mol%CaO的纳米晶体ZrO2和包含4,8、12、16和20mol%CeO 2的ZrO2。XRD,TEM和拉曼光谱法用于表征合成后的粉末。对于这两种系统,所产生的粉末均为四方晶,且晶体尺寸小于50nm。所获得的晶体尺寸随着CaO / CeO2含量的增加而减小。对于CaO-ZrO2系统,产生的ZrO2的主要缺陷是Cazr''和Vo··。氧空位位于与Ca2 +最接近的位置。 Ca2 +的配位数为7。对于CeO2-ZrO2系统,制得的粉末既不存在Ce2O3,也不存在明显的氧空位。在ZrO2中Ce4 +的配位数为8。目前对CeO2-ZrO2系统的研究遵循了维加德定律。在当前的研究中,使用热等静压(HIPing)成功地将合成后的ZrO2-6、8和10mol%CaO和ZrO2-12、16和20mol%CeO2粉末致密化,保留了纳米晶尺寸和四方结构。力学性能测试发现,随着上述组合物中CaO / CeO2含量的增加,硬度增加而断裂韧性降低。纳米晶氧化锆的硬度和断裂韧性低于粗晶氧化锆。对于ZrO2-6mol%CaO,获得的硬度为3.8GPa,断裂韧性为4.10MPa.m1 / 2。对于ZrO2-12mol%CeO2,获得的硬度为2.9GPa,断裂韧性为5.18MPa.m1 / 2。获得的这些特性可以通过晶界滑动和不存在相变增韧来解释。在当前研究中开发的HIPing模型表明,在HIPing的初始阶段,扩散优先于幂律蠕变,而在纳米晶氧化锆的HIPing的最后阶段,晶界扩散优先于晶格扩散。

著录项

  • 作者

    Zhou, Enhong.;

  • 作者单位

    University of Idaho.;

  • 授予单位 University of Idaho.;
  • 学科 Engineering Materials Science.; Engineering Metallurgy.
  • 学位 Ph.D.
  • 年度 2000
  • 页码 164 p.
  • 总页数 164
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 工程材料学;冶金工业;
  • 关键词

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