4.8 Article

Development and Testing of Diglycolamide Functionalized Mesoporous Silica for Sorption of Trivalent Actinides and Lanthanides

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 7, 期 37, 页码 20591-20599

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.5b04481

关键词

europium; americium; separations; mesoporous silica; diglycolamide; solid-state NMR

资金

  1. National Nuclear Security Administration (NNSA) under Stewardship Science Academic Alliance Program [DE-NA0001978]
  2. Subsurface Biogeochemical Research Program of the U.S. Department of Energy's Office of Biological and Environmental Research
  3. U.S. Department of Energy by Lawrence Livermore National Laboratory [DE-AC52-07NA27344]
  4. DOE NNSA Stewardship Science Graduate Fellowship [DE-NA0002135]
  5. National Science Foundation Graduate Research Fellowship [DGE 1106400]

向作者/读者索取更多资源

Sequestration of trivalent actinides and lanthanides present in used nuclear fuel and legacy wastes is necessary for appropriate long-term stewardship of these metals, particularly to prevent their release into the environment. Organically modified mesoporous silica is an efficient material for recovery and potential subsequent separation of actinides and lanthanides because of its high surface area, tunable ligand selection, and chemically robust substrate. We have synthesized the first novel hybrid material composed of SBA-15 type mesoporous silica functionalized with diglycolamide ligands (DGA-SBA). Because of the high surface area substrate, the DGA-SBA was found to have the highest Eu capacity reported so far in the literature of all DGA solid-phase extractants. The sorption behavior of europium and americium on DGA-SBA in nitric and hydrochloric acid media was tested in batch contact experiments. DGA-SBA was found to have high sorption of Am and Eu in pH 1, 1 M, and 3 M nitric and hydrochloric acid concentrations, which makes it promising for sequestration of these metals from used nuclear fuel or legacy waste. The kinetics of Eu sorption were found to be two times slower than that for Am in 1 M HNO3. Additionally, the short-term susceptibility of DGA-SBA to degradation in the presence of acid was probed using Si-29 and C-13 solid-state NMR spectroscopy. The material was found to be relatively stable under these conditions, with the ligand remaining intact after 24 h of contact with 1 M HNO3, an important consideration in use of the DGA-SBA as an extractant from acidic media.

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