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Title: Formation of hydroxyapatite in soils using calcium citrate and sodium phosphate for control of strontium migration.

Conference ·
OSTI ID:1004366

{sup 90}Sr contamination is a major problem at several U.S. sites. At some sites, {sup 90}Sr has migrated deep underground making site remediation difficult. In this paper, we describe a novel method for precipitation of hydroxyapatite, a strong sorbent for {sup 90}Sr, in soil. The method is based on mixing a solution of calcium citrate and sodium phosphate in soil. As the indigenous soil microorganisms mineralize the citrate, the calcium is released and forms hydroxyapatite. Soil, taken from the Albuquerque desert, was treated with a sodium phosphate solution or a sodium phosphate/calcium citrate solution. TEM and EDS were used to identify hydroxyapatite with CO{sub 3}{sup 2-} substitutions, with a formula of (Ca{sub 4.8}Na{sub 0.2})[(PO{sub 4}){sub 2.8}(CO{sub 3}){sub 0.2}](OH), in the soil treated with the sodium phosphate/calcium citrate solution. Untreated and treated soils were used in batch sorption experiments for Sr uptake. Average Sr uptake was 19.5, 77.0 and 94.7% for the untreated soil, soil treated with sodium phosphate, and soil with apatite, respectively. In desorption experiments, the untreated soil, phosphate treated soil and apatite treated soil released an average of 34.2, 28.8 and 4.8% respectively. The results indicate the potential of forming apatite in soil using soluble reagents for retardation of radionuclide migration.

Research Organization:
Sandia National Laboratories (SNL), Albuquerque, NM, and Livermore, CA (United States)
Sponsoring Organization:
USDOE
DOE Contract Number:
AC04-94AL85000
OSTI ID:
1004366
Report Number(s):
SAND2003-3112C; TRN: US201103%%519
Resource Relation:
Conference: Proposed for presentation at Chemistry and Migration Behavior of Actinides and Fission Products in the Geosphere held September 21-26, 2003 in Kyongju, Korea.
Country of Publication:
United States
Language:
English