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Interpretation of Containment Chemistry Results from Phebus Test FPT2

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55% of initial iodine inventory released to containment ... 30% of deposited iodine re-released in late aerosol and chemistry phases ... – PowerPoint PPT presentation

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Title: Interpretation of Containment Chemistry Results from Phebus Test FPT2


1
  • Interpretation of Containment Chemistry Results
    from Phebus Test FPT2

Shirley Dickinson
Nathalie Girault
Luis Herranz
Philippe Raison
2
Introduction
  • Phebus-FP tests are an important source of data
    on fission product release and transport under
    severe accident conditions
  • New insights into iodine transport in primary
    circuit and chemistry in containment
  • Focus for model development / validation /
    comparison
  • FPT2 iodine chemistry in containment
  • Summary of main results
  • Interpretation and understanding
  • Modelling studies

3
Phebus-FP facility
4
Phebus-FP facility
FPT2 containment 10 m3 steel vessel 100 dm3
aqueous sump, pH 9 Tatmosphere 90C Tsump
90C (aerosol phase), 120C (chemistry
phase) Sump evaporation atmosphere painted
condensers sump
5
Experimental observations
  • 55 of initial iodine inventory released to
    containment
  • Mainly detected in containment as aerosol
  • Small gaseous fraction during fuel degradation /
    release transient
  • No evidence for gaseous iodine in circuit
  • Iodine concentration evolution

6
Iodine evolution during degradation / aerosol
phase
7
Iodine evolution during chemistry phase
8
Experimental observations (2)
  • Final gaseous iodine concentration is lt 0.01 of
    containment inventory
  • Predominantly inorganic
  • Iodine in sump is mainly soluble
  • Contrast FPT0/1 where mainly insoluble (AgI)
  • Solubility decreased at end of test sump
    cooling
  • Decrease in iodine activity on vertical
    containment walls in late aerosol chemistry
    phase
  • Slight increase in condenser activity in late
    aerosol phase

9
Modelling studies
  • ASTEC-IODE, IMPAIR-JRC, INSPECT, MELCOR iodine
    module, IODAIR
  • Dissolution of iodide aerosol in sump I- ions
  • Radiolytic oxidation of I- I2 (volatile I)
  • Reactions of I- and/or I2 with silver AgI
    (insoluble I)
  • Partition of I2 containment atmosphere (gaseous
    I)
  • Reaction of I2 with surfaces deposited I
  • Reaction with organic impurities organic I
  • Radiolytic oxidation of gaseous I2 or RI
    involatile I
  • Input data experimental measurements, boundary
    conditions, geometry, estimated values

10
Results overall iodine distribution
  • Gross iodine behaviour is generally well
    reproduced by the models
  • Low final gaseous concentration
  • Mainly in sump or on surfaces during chemistry
    phase
  • Surface deposition not reproduced as aerosol
    mechanisms are dominant
  • Example

11
IODEv5.2 and MELCOR results iodine distribution
12
Iodine in the containment atmosphere
  • Assumption of 1 gaseous source essential to
    reproduce early behaviour
  • Origin? Circuit? Reactions on condenser surface?
  • Early peak iodine rapidly removed
  • Surface deposition transport to condensers
  • Gaseous radiolysis
  • Surfaces are not a strong sink for iodine
  • Persistent gaseous concentration throughout
    aerosol phase
  • Condensation is an efficient removal mechanism
  • Transfer of iodine to sump

13
IODEv5.2 calculation of gaseous iodine evolution
14
Iodine in the containment atmosphere (2)
  • Models suggest that organic iodide formation is
    the main source of gaseous iodine at longer times
  • I2 volatilisation from sump is insignificant
  • Decomposition of surface aerosols not modelled
  • Gas-phase radiolysis has a significant impact on
    iodine behaviour
  • Products are solid iodine oxides
  • Uncertainties in reaction mechanism airborne
    speciation
  • Aerosol formation and deposition modelling

15
INSPECT / IODAIR calculations of airborne iodine
speciation
16
Iodine in the sump
  • Measurement show mainly soluble iodine
  • Solubility decrease during washing cool-down
  • Model predictions of solubility depend on Ag
    aerosol characteristics
  • AgI formation rate depends on surface area,
    degree of oxidation both very uncertain
  • Solubility changes suggest decomposition of AgI
    not generally modelled
  • Iodine volatility from sump remains low as high
    pH and temperature suppress I2 formation

17
IODEv5.2 calculations of iodine speciation in the
sump
Deposited
Dissolved
18
Iodine release from surfaces
  • Results appear to show loss of iodine from
    containment wall deposits
  • 30 of deposited iodine re-released in late
    aerosol and chemistry phases
  • Large wall deposition in FPT2 significant
    additional gaseous iodine source
  • Possible contributor to concentration increase
  • Not included in models
  • Mechanism unknown, possible decomposition of
    iodide aerosol in containment atmosphere
  • Potential impact in reactor calculations?

19
Conclusions
  • Modelling of iodine behaviour in FPT2 containment
  • Detailed mechanistic models integral code
    modules
  • Reasonable success in reproducing the main
    aspects
  • Relative importance of phenomena varies between
    codes
  • Consensus reached in many areas
  • Potentially important uncertainties remain
  • Radiolytic oxidation of gaseous species identity
    and behaviour of products

20
Conclusions (2)
  • Early gaseous iodine peak cannot be accounted for
    by reactions in sump
  • Radiolysis of gaseous species involatile
    species
  • Important influence on airborne iodine behaviour
  • Iodine chemistry in sump not dominated by AgI
  • Volatility suppressed by high pH, T
  • Details of solubility behaviour not understood
  • Evaporating/condensing conditions low
    steady-state I concentration in the containment
    atmosphere
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