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Development of pillared M(IV) phosphate phosphonate inorganic organic hybrid ion exchange materials for applications in separations found in the nuclear fuel cycle.

机译:开发用于核燃料循环中分离的柱状磷酸M(IV)膦酸酯无机有机杂化离子交换材料。

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摘要

This dissertation focuses on key intergroup and intragroup separations found in the back end of the nuclear fuel cycle, specifically americium from lanthanides and americium from other actinides, most importantly americium from curium. Our goal is to implement a liquid-solid separation process to reduce waste and risk of contamination by the development of metal(IV) phosphate phosphonate inorganic organic hybrid ion exchange materials with the ideal formula of M(O6P2C6H4)0.5 (O3POA) ·nH2O, where M = Zr or Sn, A = H or Na. These materials have previously shown to have high affinity for Ln, this work will expand on the previous studies and provide methods for the above target separation, exploiting oxidation state and ion charge to drive the separation process.;The optimum hydrothermal reaction conditions were determined by adjusting parameters such as reaction temperature and time, as well as the phosphonate to phosphate (pillar-to-spacer) ligands ratio. Following these results four bulk syntheses were performed and their ion exchange properties were thoroughly examined. Techniques such as inductively coupled mass spectrometry and liquid scintillation counting were used to determine the affinity of the materials towards Na+, Cs+, Ca2+, Sr 2+, Ni2+, Nd3+, Sm3+, Ho3+, Yb3+, NpO2+, Pu4+, PuO22+, Am3+, AmO2+, and Cm3+.;Separation factors in the thousands have been observed for intergroup separations of the Ln from the alkali, alkaline earth, and low valent transition metals. A new method for Am oxidation was developed, which employed Na 2S2O8 as the oxidizing agent and Ca(OCl) 2 as the stabilizing agent for AmO2+ synthesis. Separation factors of 30-60 for Nd3+ and Eu3+ from AmO2+, as well as 20 for Cm3+ from AmO2+ were observed at pH 2. The work herein shows that a liquid-solid separation can be carried out for these difficult separations by means of oxidation and ion exchange.
机译:本文主要研究核燃料循环后端的关键族间和族内分离,特别是镧系元素from和其他a系元素,,最重要的是cur元素。我们的目标是通过开发具有理想分子式M(O6P2C6H4)0.5(O3POA)·nH2O的磷酸金属膦(IV)无机有机杂化离子交换材料,来实现液固分离工艺,以减少浪费和污染风险。其中M = Zr或Sn,A = H或Na。这些材料先前已显示出对Ln的高亲和力,这项工作将在先前的研究基础上进行扩展,并提供用于上述目标分离的方法,利用氧化态和离子电荷来驱动分离过程。调整参数,例如反应温度和时间,以及膦酸酯与磷酸酯(柱对垫片)的配体比例。根据这些结果,进行了四次本体合成,并对其离子交换性能进行了彻底的检查。使用电感耦合质谱法和液体闪烁计数等技术确定材料对Na +,Cs +,Ca2 +,Sr 2 +,Ni2 +,Nd3 +,Sm3 +,Ho3 +,Yb3 +,NpO2 +,Pu4 +,PuO22 +,Am3 +,AmO2 +的亲和力Ln与碱金属,碱土金属和低价过渡金属的族间分离已观察到数千种分离因子。开发了一种新的Am氧化方法,该方法以Na 2S2O8为氧化剂,Ca(OCl)2为AmO2 +合成的稳定剂。在pH 2下,Nd3 +和Eu3 +与AmO2 +的分离系数为30-60,Cm3 +与AmO2 +的分离系数为20。本文的工作表明,对于这些困难的分离,可以通过氧化和液相进行液-固分离。离子交换。

著录项

  • 作者

    Burns, Jonathan David.;

  • 作者单位

    Texas A&M University.;

  • 授予单位 Texas A&M University.;
  • 学科 Chemistry General.;Chemistry Organic.;Engineering Materials Science.;Chemistry Inorganic.
  • 学位 Ph.D.
  • 年度 2012
  • 页码 168 p.
  • 总页数 168
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:43:36

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