Estimation of Tritium Recovery from a Molten Salt Blanket of FFHR Dept. Applied Quantum Physics and Nuclear Engineering, Kyushu University Satoshi FUKADA.

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Estimation of Tritium Recovery from a Molten Salt Blanket of FFHR Dept. Applied Quantum Physics and Nuclear Engineering, Kyushu University Satoshi FUKADA US/Japan Workshop on Power Plant Studies and Related Advanced Technologies with EU Participation, April 6-7, 2002 (San Diego, CA)

1. Background study : Characteristics of Flibe as a self-cooled blanket Advantages (1) liquid blanket, low reactivity with air or water (2) low MHD effect (3) TBR >1 with addition of Be and low tritium solubility FFHR or HYLIFE-II Disadvantages (1) less Flibe-facing structural materials under neutron irradiation (2) unknown tritium behavior or recovery in Flibe is not studied. (3) possibly high tritium leak to the environment (4) issues of Be safety JUPITER-II Relating to this study

Design activities in NIFS Collaboration Now, on going cf. NIFS annual repo.

1. Background study : Tritium recovery from Flibe relating to the things (1) Physical Properties (Underlined properties are not available or not reliable) Tritium solubility (TF or T 2 ) Tritium diffusivity, permeation coefficient or mass-transfer coefficient Viscosity, thermal diffusivity or heat-transfer coefficient Phase diagram, vapor pressure, free energy change of fluoride formation Estimated from H 2, D 2 or other data (2) Affecting factors Chemical forms of tritium in Flibe, T 2, TF or T 2 O, or Flibe purification REDOX control condition, change from TF to T 2 Corrosive HF or TF in Flibe Isotopic effect and coexistent components to use purified Flibe and REDOX control by Be

1. Background study : Necessary conditions imposed on apparatus of tritium recovery from Flibe All tritium generated in a blanket is recovered Very low tritium leak to the environment Simple apparatus and easy to operate Operation over melting temperature High operation safety and material compatible with HF M+nHF ⇨ MF n +(n/2)H 2 Operated under low water vapor condition BeF 2 +2H 2 O≠Be(OH) 2 +2HF, LiF+H 2 O≠LiOH+HF Permeation window, He-Flibe counter-current column, Vacuum disengager

2. Design study : Design of tritium-recovery apparatus for FFHR Assumptions Based on FFHR design Steady-state operation Tritium generated in a blanket is transferred by Flibe and is recovered by a tritium recovery apparatus. No isotope effect in properties No decomposition of Flibe by VxB We focused on whether or not tritium can be recovered by a realistic scale of apparatus. Table 1 FFHR parameters on tritium recovery What is the rate-determining step of tritium recovery

Tritium generation rate (1 GW t ) 190 g -T /day = 1.8 MCi/day Tritium recovery system Heat exchanger x in ( = K H p in or = K S p in 0.5 ) x out ( = K H p out or = K S p out 0.5 ) Tritium leak rate to the environment 〜 10 Ci/day K p A in p in K p A out p out others Tritium leak rate 〜 K p A in p in C 470C Flibe flow rate 2.3m 3 /s Tritium storage Tritium leak rate 〜 K p A out p out 0.5 Be pebbles 2. Design study : Flow of Flibe and tritium Tritium recovery system Bypass ratio  Flibe blanket Tritium permeation barrier pump

2. Design study : Evaluation of tritium leak no barrier for tritium leakIf there is no barrier for tritium leak, Q leak = 2x10 -3 mol -T /s = 5 MCi/day huge tritium leak (A=10 2 m 2, p T2 =10 3 Pa, K p =3.15x mol/msPa 0.5 (ferrite), t=5mm) impossible to lower the tritium leak rate, < Pa surrounded by a stagnant Flibe (or Flinak) layer (barrier)If the heat exchanger or the tritium recovery system is surrounded by a stagnant Flibe (or Flinak) layer (barrier), Q leak = 6x mol -T /s = 1.6Ci/day allowable tritium leak ( A=10 2 m 2, p T2 =10 3 Pa, D T =5x10 -9 m 2 /s, K H =3.2x10 -7 mol/m 3 Pa, t=50cm ) Other reliable tritium barrier with a factor of 10 6 is OK, if available (e.g. alumina)

2. Design study : Material balance of tritium in Flibe Necessary conditions Q T =1.8MCi/day Q leak <10Ci/day Design of economic apparatus Fig. 2 Relation between c in and c out  =0.1 is possible if 50cm shield is present allowable

Permeation window Flibe in Flibe out He in He out Permeation material Tritium permeation Tritium permeation barrier (stagnant Flibe) Fig. 3 Permeation window system Tritium getter

2. Design study : Tritium transfer process in Flibe-facing material Processes include (1) (1) Tritium (TF or T 2 ) generation rate in Flibe (2) (2) Tritium (TF or T 2 ) diffusion in Flibe (3) (3) Tritium (TF or T 2 ) solution in Flibe (4) (4) Tritium migration from Flibe surface to metal surface (impurity layer) (5) Tritium (T) permeation through metal (6) (6) Desorption or absorption of tritium (TF or T 2 ) from Flibe (7) Tritium (TF or T 2 ) diffusion in gas (8) Tritium recombination on metal surface ( ) unique to Flibe Fig. 4 Mass transfer processes from Flibe to gas phase

Fig. 5 Rate-determining step of the overall tritium permeation Fluid Flibe film Impurity migration Permeation 2. Design study : Rate-determining step of permeation window dirty clean

2. Design study : Design equations of permeation window Permeation material : Ni, or ferritic steel Upstream side : (purified) Flibe Downstream side : He purge Overall resistance of mass-transfer of tritium permeation Tritium generated in blanket, Q T, is all recovered by permeation window. Fig. 5 Permeation window tritium recovery system Diffusion in FlibePermeation through wall 2.3m 3 /s

2. Design study : Estimation of permeation window area Tritium recovery is easy at high tritium pressure (concentration) ⇨ high tritium leak Tritium recovery is difficult at low tritium pressure (concentration) ⇨ large apparatus Operation at around x T =0.2 ppm satisfies 10Ci/day limit and 190g/day recovery Resistances of Flibe-film diffusion is controlling and permeation gives a small effect Fig. 6 Permeation window area (  =1, t=1mm) Tritium leak Large apparatus

Flibe in Flibe out He out He in Downward Flibe flow Upward He flow Counter-current extraction tower Tritium permeation barrier (stagnant Flibe) Raschig ring packing Fig. 8 Flibe-He counter-current extraction tower Perforated plate Tritium getter

Material balance equation Gas-phase height transfer unit Flibe-phase height transfer unit Concentration profile (Solution) 2. Design study : Design equations for He extraction tower Fig. 9 Concentration change in extraction tower Rate-determining step is liquid phase diffusion.

Tritium concentration in He almost increases logarithmically. Tritium concentration in Flibe almost decreases logarithmically of DF for Flibe-tritium system is possible by 5 m extraction tower. 190 g/day tritium can be recovered by one extraction tower. Values of H L are unsure because they are not determined by Flibe experiment but by water-hydrogen system. (HTU) L >> (HTU) G 2. Design study : Tritium concentration in He extraction tower Fig. 10 Tritium concentration in He extraction tower  =0.1)

2. Design study : Analysis of vacuum disengager Assumptions Flibe drops free fall from the top and dissolved tritium is desorbed by a vacuum pump. d p =2mm, h=10m,  =0.1 Surface recombination resistance is ignored. Drop formation energy 〜 1.4kW Pumping power for perforation 〜 160kW Fig.11 Concentration profile in disengager

2. Design study : Conclusions from design study Need a tritium barrierNeed a tritium barrier to control tritium leak below 10Ci/day stagnant FlibeAs long as the tritium leak rate is lower than the permissible level (e.g. by stagnant Flibe), arranging the tritium recovery system in a by-pass line is effective. permeation window, extraction column and vacuum disengager are a realistic- scale apparatusIn that case, the recovery systems of the permeation window, extraction column and vacuum disengager are a realistic- scale apparatus. Diffusion in fluid Flibe is the rate-determining stepDiffusion in fluid Flibe is the rate-determining step in the permeation window and He-Flibe counter-current column. In order to raise the accuracy of the design, the mass-transfer coefficient from Flibe to extraction gas should be clearly determined.

Flinabe 2. Design study : On Flinabe as a blanket material (LiF-NaF-BeF 2 ) advantages Low melting point (=240C?), low operation temperature TBR>1 may be possible with addition of Be. Other physical properties may be similar to Flibe disadvantages Activation of Na (formation of 22 Na or 24 Na) There are no data available on tritium mass-transport More data are necessary for the design of the tritium recovery system