Published June 14, 2000 | Version v1
Report

Physical, chemical, and structural evolution of zeolite-containing waste forms produced from metakaolinite and calcined HLW

Description

Natural and synthetic zeolites are extremely versatile materials. They can adsorb a variety of liquids and gases, and also take part in cation exchange reactions. Zeolites have the ability to sequester ions in lattice positions or within their networks of channels and voids. The zeolites can host alkali, alkaline earth and a variety of higher valence cations. As such they may be a viable alternative for immobilization of low activity waste (LAW) salts and calcines. The process for synthesizing zeolites is well documented for pure starting materials. A reactive aluminosilicate is reacted with an alkaline hydroxide at low temperature to form a zeolite. Processing time and temperature and specific reactants determine the type of zeolite formed. Zeolites are easy to make, and can be synthesized from a wide variety of natural and man made materials. However, relatively little is known about the process if one of the starting materials is a poorly characterized complex mixture of oxides (waste) containing nearly every element in the periodic table. The purpose of this work is to develop a clearer understanding of the advantages and limitations of producing a zeolite waste form from radioactive waste. Dr. M. W. Grutzeck at the Pennsylvania State University is investigating the production of a zeolite waste form using non-radioactive simulants. Dr. C. M. Jantzen and J. M. Pareizs at the Savannah River Technology Center will use the results from simulant work as a starting point for producing a zeolite waste form from an actual Savannah River Site radioactive waste stream

Availability note (English)

Available from PURL: https://www.osti.gov/servlets/purl/756743-fM5J5L/webviewable/

Additional details

Publishing Information

Imprint Pagination
[vp.]
Report number
WSRC-TR--2000-00198

Optional Information

Contract/Grant/Project number
AC09-96SR18500
Notes
This record replaces 31033243
Funding organization
US Department of Energy (United States)