Published September 17, 2012 | Version v1
Journal article

Single Phase Melt Processed Powellite (Ba,Ca) MoO4 For The Immobilization Of Mo-Rich Nuclear Waste

  • 1. Savannah River Site (SRS), Aiken, SC (United States)
  • 2. Pacific Northwest National Laboratory, Richland, WA (United States)
  • 3. Los Alamos National Laboratory, Los Alamos, NM (United States)

Description

Crystalline and glass composite materials are currently being investigated for the immobilization of combined High Level Waste (HLW) streams resulting from potential commercial fuel reprocessing scenarios. Several of these potential waste streams contain elevated levels of transition metal elements such as molybdenum (Mo). Molybdenum has limited solubility in typical silicate glasses used for nuclear waste immobilization. Under certain chemical and controlled cooling conditions, a powellite (Ba,Ca)MoO4 crystalline structure can be formed by reaction with alkaline earth elements. In this study, single phase BaMoO4 and CaMoO4 were formed from carbonate and oxide precursors demonstrating the viability of Mo incorporation into glass, crystalline or glass composite materials by a melt and crystallization process. X-ray diffraction, photoluminescence, and Raman spectroscopy indicated a long range ordered crystalline structure. In-situ electron irradiation studies indicated that both CaMoO4 and BaMoO4 powellite phases exhibit radiation stability up to 1000 years at anticipated doses with a crystalline to amorphous transition observed after 1 X 1013 Gy. Aqueous durability determined from product consistency tests (PCT) showed low normalized release rates for Ba, Ca, and Mo (>0.05 g/m2)

Availability note (English)

Available from: DOI:10.1016/j.jallcom.2012.09.049

Additional details

Publishing Information

Journal Title
Journal of Alloys and Compounds
Journal Volume
551
Journal Page Range
33 p.
ISSN
0925-8388

Optional Information

Contract/Grant/Project number
DE-AC09-08SR22470
Funding organization
USDOE (United States)
Secondary number(s)
SRNL-STI--2012-00569; OSTI--1053795