Published May 2014 | Version v1
Journal article

Performance of the Fluidized Bed Steam Reforming product under hydraulically unsaturated conditions

  • 1. Pacific Northwest National Laboratory, Richland, WA 99352 (United States)
  • 2. Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States)

Description

Several candidates for supplemental low-activity waste (LAW) immobilization at the Hanford site in Washington State, USA are being considered. One waste sequestering technology considered is Fluidized Bed Steam Reforming (FBSR). The granular product resulting from the FBSR process is composed primarily of an insoluble sodium aluminosilicate matrix with the dominant phases being feldspathoid minerals with a 1:1:1 molar ratio of Na, Al and Si. To demonstrate the durability of the product, which can be disposed of at the unsaturated Integrated Disposal Facility (IDF) at Hanford, a series of tests has been performed using the Pressurized Unsaturated Flow (PUF) system, which allows for the accelerated weathering of the solid materials. The system maintains hydraulically unsaturated conditions, thus mimicking the open-flow and transport properties that will be present at the IDF. Two materials were tested using the system: 1) the FBSR granular product and 2) the FBSR granular product encapsulated in a geopolymer to form a monolith. Results of the experiments show a trend of relatively constant effluent concentration of Na, Si, Al, and Cs as a function of time from both materials. The elements I and Re show a steady release throughout the yearlong test from the granular material but their concentrations seem to be increasing at one year from the monolith material. This result suggests that these two elements may be present in the sodalite cage structure rather than in the predominant nepheline phase because their release occurs at a different rate compared to nepheline phase. Also, these elements to not seem to reprecipitate when released from the starting material. Calculated one-year release rates for Si are on the order of 10−6 g/(m2 d) for the granular material and 10−5 g/(m2 d) for the monolith material while Re release is seen to be two orders of magnitude higher than Si release rates. SEM imaging and XRD analysis show how the alteration of the two materials is dependent on their depth in the column. This phenomenom is a result of depth-dependent solution concentrations giving rise chemical environments that may be supersaturated with respect to a number of mineral phases. - Highlights: • Hanford waste vitrification does not adequately address secondary wastes. • Sodium-aluminosilicates have the capacity to incorporate contaminants in a stable minerals. • Fluidized Bed Steam Reforming successfully converts simulated Hanford tank waste to sodium-aluminosilicate minerals

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jenvrad.2013.10.008

Additional details

Identifiers

DOI
10.1016/j.jenvrad.2013.10.008;
PII
S0265-931X(13)00223-3;

Publishing Information

Journal Title
Journal of Environmental Radioactivity
Journal Volume
131
Journal Page Range
p. 119-128
ISSN
0265-931X
CODEN
JERAEE

Conference

Title
12. international conference on the biogeochemistry of trace elements (ICOBTE)
Acronym
ICOBTE 2013
Dates
16-20 Jun 2013
Place
Athens, GA (United States)

Optional Information

Copyright
Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.