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Dynamic project management methodology: Managing schedule compression.

机译:动态项目管理方法:管理进度压缩。

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摘要

Three different types of nanophosphor materials were prepared by flame spray pyrolysis (FSP) from nitrate-based liquid precursor. Rare-earth doped binary oxide nanophosphor particles were obtained from urea-added liquid precursor using FSP without post-heat treatment. Also, rare-earth doped ternary oxide nanophosphors were prepared from urea-added using FSP with less annealing temperature and reduced time. In addition, metal-ion doped ternary oxide nanophosphors could be easily generatred by FSP from nitrate-based liquid precursor. The prepared phosphor particles properties such as crystallinity, luminescence properties, surface morphology and particle size were investigated by many techniques in order to obtain the optimum condition for high quality nanophosphor particles.;Firstly, Y2O3:Eu3+ nanophosphor was synthesized by FSP from nitrate-based liquid precursor. Urea was added to the liquid precursor to enhance the crystallinity of Y2O 3:Eu3+ phosphor particles. The resultant phosphor particles showed Y2O3:Eu3+ cubic phase in the XRD pattern without the need for post-heat treatment. The influence of synthesis conditions such as different molar concentrations of urea, overall molar concentration of liquid precursors, and doping concentration on luminescent properties was investigated. The particle size of product was found to be in the range of 20--30 nm as determined from transmission electron microscopy (TEM) images. Photoluminescence (PL) measurement of the synthesized Y2O 3:Eu3+ nanophosphor show peak in red region of visible spectrum with a maximum peak at wavelength of 609 nm when excited with 398 nm wavelength photons.;Secondly, YAG:Ce3+ nanophosphors were synthesized by FSP from nitrate-liquid precursor. As-prepared nanoparticles were annealed in the temperature range of 800°C to 1100°C for 1 hour. The influence of addition of urea and the molar ratio of yttrium to aluminum in the liquid precursor on crystallinity and luminescence properties of YAG:Ce3+ nanophosphor particles were studied. The heat-treated phosphor particles were spherical in shape with an average size blow 50 nm. The crystallinity of YAG:Ce3+ nanophosphors improved with addition of urea and overloaded aluminum in starting liquid precursor. In addition, high PL intensity with pure YAG:Ce3+ phase was observed for phosphor particles prepared with addition of urea and excess of aluminum in liquid precursor with less annealing temperature and reduced time compared to other methods.;Green emitting Zn2SiO4:Mn2+ phosphor particles were synthesized by FSP from a function of different liquid precursors. Luminescence and crystalline properties were investigated as the different Zn-source materials in aqueous precursor. Also, the influence of post-heat treatment temperatures on the crystal structure and PL intensity of Zn 2SiO4:Mn2+ nanophosphors was investigated. Mn-doped zinc silicate crystalline structures were obtained when annealed at 1000°C for 1hour. The emission peak was found at 525 nm. Furthermore, the effect of the flame temperatures by varying methane flow rate on the crystallinity and luminescence properties of Zn2SiO 4:Mn2+ nanophosphors was investigated. The phosphor particles prepared from high flame temperature showed good crystallinity with pure zinc silicate phase and the maximum PL intensity. We conclude that different experimental conditions such as liquid precursor prepared from different Zn-source and annealing temperature influence both crystallinity and the luminescence properties of Zn2SiO4:Mn2+ nanophosphors.
机译:通过火焰喷涂热解法(FSP)从硝酸盐基液体前驱体中制备了三种不同类型的纳米磷光体材料。稀土掺杂的二元氧化物纳米磷光体颗粒是使用FSP在不经过后热处理的情况下从添加尿素的液态前驱体中获得的。另外,使用FSP从添加尿素的稀土掺杂三元氧化物纳米荧光粉制备中,退火温度更低,时间更短。此外,FSP可以很容易地从硝酸盐基液态前体中生成金属离子掺杂的三元氧化物纳米荧光粉。通过多种技术研究了所制备的荧光粉的结晶度,发光性能,表面形貌和粒径等性能,从而为获得高质量的纳米荧光粉提供了最佳条件。首先,FSP由硝酸盐基合成了Y2O3:Eu3 +纳米荧光粉。液体前体。将尿素添加到液体前体中以增强Y2O 3:Eu3 +荧光粉颗粒的结晶度。所得的磷光体颗粒在X射线衍射图中显示出Y 2 O 3:Eu 3+立方相,而无需进行后热处理。研究了合成条件的影响,例如不同的尿素摩尔浓度,液体前体的总摩尔浓度和掺杂浓度对发光性能的影响。由透射电子显微镜(TEM)图像确定,发现产物的粒度在20--30nm范围内。合成的Y2O 3:Eu3 +纳米磷光体的光致发光(PL)测量显示,在398 nm波长的光子激发下,可见光光谱的红色区域出现一个峰值,最大波长为609 nm;其次,由FSP合成了YAG:Ce3 +纳米磷光体。硝酸盐液体前体。将制备好的纳米颗粒在800°C至1100°C的温度范围内退火1小时。研究了液态前驱物中尿素的添加以及钇与铝的摩尔比对YAG:Ce3 +纳米磷光体颗粒结晶度和发光性能的影响。热处理的荧光体颗粒为球形,平均尺寸为50nm。 YAG:Ce3 +纳米磷光体的结晶度通过在起始液体前体中添加尿素和过量的铝而得到改善。此外,与其他方法相比,在液态前体中添加尿素和过量铝而制备的荧光粉颗粒具有较高的PL强度,具有纯YAG:Ce3 +相,与其他方法相比具有更低的退火温度和更少的时间;绿色发光的Zn2SiO4:Mn2 +荧光粉颗粒为由FSP根据不同液体前体的功能合成。作为水性前体中不同的锌源材料,研究了发光和晶体性质。此外,研究了后热处理温度对Zn 2SiO4:Mn2 +纳米磷光体晶体结构和PL强度的影响。当在1000℃下退火1小时时,获得了掺杂Mn的硅酸锌晶体结构。在525nm处发现发射峰。此外,研究了甲烷温度变化引起的火焰温度对Zn2SiO 4:Mn2 +纳米磷光体结晶度和发光性能的影响。由高火焰温度制备的荧光粉颗粒具有良好的结晶度,具有纯硅酸锌相和最大PL强度。我们得出结论,不同的实验条件,例如由不同的锌源和退火温度制备的液体前体,会影响Zn2SiO4:Mn2 +纳米磷光体的结晶度和发光性能。

著录项

  • 作者

    Lee, Jaesung.;

  • 作者单位

    University of Florida.;

  • 授予单位 University of Florida.;
  • 学科 Engineering Civil.
  • 学位 Ph.D.
  • 年度 2008
  • 页码 141 p.
  • 总页数 141
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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