Fission Fragment Diffusion Through TRISO

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File:DE-FOA-001515.pdf

Text from Appendix A

RADIOISOTOPE RETENTION IN GRAPHITE AND GRAPHITIC MATERIALS (RC-2) (FEDERAL POC – MADELINE FELTUS & TECHNICAL POC – PAUL DEMKOWICZ) (ELIGIBLE TO LEAD: UNIVERSITIES ONLY) (UP TO 3 YEARS AND $800,000)

Graphite is a primary core material across multiple types of advanced reactors (i.e., HTGR, FHR, and MSR) which have common material issues such as irradiation-induced material property changes, chemical reactivity, and material degradation. Fundamental studies determining the underlying mechanisms driving the material behavior as well as the impact from these effects on the core behavior is required for design and licensing can be completed for these advanced reactor concepts. A major issue of concern for MSR, FHR, and VHTR designs is the retention of activated fission products within graphite and graphitic materials such as the graphitic matrix composite used in TRISO particle fuel forms (pebbles or compacts). Radioactive material of fission product release from the fuel or from neutron reactions with molten coolant and fuel (lithium in FLiBe or FLiNaK in MSR designs) can be retained in carbon matrix, carbon-carbon composites, and graphite components. Research is needed on those graphite properties that are important for retention (and potential release) of these radioisotopes from a material possessing a graphitic crystal structure. Of particular interest is the chemisorption potential for various species, RSA efficiency, diffusion and intercalation efficiency, microstructure effects (grain size, BET, porosity distribution, source material), and at partial pressures of hydrogen (tritium and entrained water) over a range of high temperatures (500-1600C). This will assist in determining total inventory of retained products for accurate source term calculations required for licensing, determining the possibilities of tritium removal from carbon-based materials, and core component performance issues. The sorption/desorption isotherms of key fission products (including silver, cesium, strontium, and europium) in irradiated nuclear grade graphites for the high temperature reactors need to be determined. Research projects may use un-irradiated graphitic material and non-radioactive isotopes of the key fission products as surrogates to determine fission product retention behavior; however, comparison of parameters with the results from irradiated TRISO fuel forms and irradiated graphite experiments is encouraged. The objective of this project is to assess the retention of activated fission products within graphite as a function of the microstructural, fission product, and environmental conditions examined. Overall project results should include a description of all experimental conditions examined, analytical methods employed, and resulting effects on transport and retention of the various species examined.

Irradiate and perform PAA on graphite films

Fission Fragments of Interest That are measurable with PAA

strontium

The Reaction
8838Sr50+γ8738Sr49+10n , 2.8 hr , 388.5 keV

lesser abundant natural isotopes

8638Sr48+γ8538Sr47+10n, 67 minute, 232 keV
8738Sr49+γ8638Sr48+10n
8438Sr46+γ8338Sr45+10n

Proton knockout makes nuclear waste beta emitter (Rb) that decays to Se-87

8838Sr50+γ8737Rb50+11p8738Sr49+01β

silver

The Reaction
10747Ag60+γ10647Ag59+10n, 8.3 day, 451 keV
10947Ag62+γ10847Ag61+10n, 23 minute half life, 511 keV is dominant gamma line

cesium

The Reaction
13355Cs78+γ13255Cs77+10nγ13254Xe76+01β, 6 days, 667 keV

europium

The Reaction
15163Eu88+γ15063Eu87+10n, 37 yrs, 334, 439 , 584 keV
15163Eu88+γ15063Eu87+10n15062Sm88+01β+, 13 hrs, 334, 406 keV
15363Eu90+γ15263Eu89+10n, 96 min, 90 keV

References

File:Carter 2015 Thesis4DiffusionInGraphite.pdf

PAA_Research

Ag Diffusion

File:Gerczak JNM 2015.pdf

File:VanRooyen HTR2014prodceedings.pdf


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