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Idaho National Engineering and Environmental Laboratory Update on IFE Safety Work for ARIES David Petti Fusion Safety Program ARIES e-meeting October 17, 2001

ARIES IFE safety talk 901 -  · Update on IFE Safety Work for ARIES David Petti ... (150 to 550°C), ... LiOH aerosol is also formed if water vapor

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Idaho National Engineering and Environmental Laboratory

Update on IFE SafetyWork for ARIES

David PettiFusion Safety Program

ARIES e-meetingOctober 17, 2001

Idaho National Engineering and Environmental Laboratory

Several safety issues for IFE designsare being studied• Target fabrication safety and reliability issues• Risk assessment accident-initiating events• Coolant hazards (Sn, Pb, Sn-25Li)

– Chemical reactivity– Chemical toxicity– Radiological hazards

• Aerosol considerations for chamber clearing

Idaho National Engineering and Environmental Laboratory

Manufacturing industry input for IFEtarget fabrication• INEEL and GA personnel visited Micron Technology

(Boise, ID) on July 18 to gather information aboutmanufacturing processes for precision, high quality,large scale production.

• Highlights of the Micron facility:– produces on the order of 400,000 chips/day– clean room facilities are large and expensive (i.e.,

$3k/foot2).– 1.5 mile tour to visit the manufacturing stations

• Micron staff members were enthused about potentialcollaboration(s) to support IFE target manufacture.

Idaho National Engineering and Environmental Laboratory

Industry input on manufacturingquality assurance• Quality Assurance data about the Micron facilities:

– an initial production run may have 50% defects,while a mature run has less than 10% defects.

– batches from an initial production run are tested upto 130 hrs while mature runs are tested up to 10 hrs.

– an estimated four to five “end user product” returnsper million units distributed.

– facility support services are tightly controlled tomaintain manufacturing quality.

– electrostatic suppression and discharge are veryimportant for maintaining high-quality production.

Idaho National Engineering and Environmental Laboratory

Accident initiating events are beingcompiled for IFE designs• Current initiator work is focused on the SOMBRERO

design.– SOMBRERO is representative of dry wall, laser driver

IFE design concepts• A master logic diagram (MLD) for SOMBRERO has been

drafted and is under review. The MLD is a plant-levelfault tree of potential hazardous releases.

• An MLD for the HYLIFE II plant design has been initiatedand will be completed later this year.– HYLIFE II is representative of liquid wall, ion beam

driver IFE design concepts

Idaho National Engineering and Environmental Laboratory

Coolant hazards: chemical reactivity• Queries of the HSC chemistry database program show:

– molten Pb, Sn, and Sn-25Li exothermically react withair and potentially result in limited aerosol generation;

– liquid Sn exothermically forms SnO2 in abundant air orSnO in limited air;

– at low temperatures (150 to 550°C), liquid Pb in airexothermically forms gaseous Pb2O3. Above 550°C,the gas dissociates into PbO gas and PbO2. ThePbO2 will potentially form aerosol;

• Li and Sn individually react in air to form chemically toxicspecies, thus the same behavior is anticipated for Sn-25Li in air.

Idaho National Engineering and Environmental Laboratory

Coolant hazards: chemical reactivity(cont)• Li dehydrates concrete: reaction rates are low in the

200°C range and increase in the 400°C range.• In the 400 °C range, other liquid metals will also dehydrate

concrete. Thus safety design provisions are required.• Li reacts in air to form Li2O and generate 3-10%wt respir-

able aerosol. LiOH aerosol is also formed if water vaporis present in the air (HEDL TME 80-79; HEDL TME 85-25)

• Molten Pb-Li and Sn-Li will react with water to releasehydrogen gas (M. H. Anderson, 14th TOFE).

Idaho National Engineering and Environmental Laboratory

Coolant hazards: chemical toxicity• Li, Pb, Sn, and Sn-25Li have un-irradiated chemical

safety concerns.• DOE has established Temporary Emergency Exposure

Levels (TEELs) for aerosol inhalation of chemicalsubstances by the general public.

• The DOE-Idaho Operations Office recommends TEEL-2as a prudent 1-hour maximum exposure level for publicsafety.

• DOE-HQ has not yet released guidance on exposurelevels for chemical releases in energy research.

Idaho National Engineering and Environmental Laboratory

TEELs for candidate IFE coolantsM a terial T E E L -0

(mg/m 3)T E E L -1(mg/m 3)

T E E L -2(mg/m 3)

T E E L -3(mg/m 3)

T in(S n )

2 6 10 100

T in oxide(S n O )

2 6 10 100

L ith ium(L i)

10 30 50 500

L ith iumox ide(L i2O )

-- -- A IHA c i tes1 m g /m 3 forw o rkers =

T E E L -2

--

L ith iumhydrox ide

(L i O H )

0 .05 0 .15 1 100

Lead(P b )

0 .05 0 .15 0 .25 100

Lead ox ides(P b O a n d

P b O 2)

0 .05 0 .05 0 .05 100

T E E L L e v e lH e a lthE ffec ts

n ohea ltheffects

m ild ,trans ient

effects

ser ious,trans ient

effects

life can bethreatenedpast 1 h o u r

exposuren o te: T E E L s a re fro m rep o rt W S M S -SAE-00-0266, rev is ion 17m , January2001 . See a lso W S R C -TR-98-00080, “M e thodo logy for Der iv ing T E E L s ,”A p ril 1998 .

Idaho National Engineering and Environmental Laboratory

Coolant hazards: radiological concerns• A radiological-based analysis of the coolants focused on

five factors:– Decay heat generation: influences accident response– Contact dose (gamma): influences worker safety and

maintenance– Vapor pressure: volatility under air in steam ingress

condition– Radiotoxicity: identifies the isotopes whose activity

levels produce radiation concerns– Class C waste: identifies materials that can meet the

low level waste criteria

Idaho National Engineering and Environmental Laboratory

Decay heat comparison

From: C.B.A. Forty et. al., Handbook of Fusion Activation Data, Part 1, AEA FUS 180, May 1992 and Part 2, AEA FUS 232,May 1993, AEA Technology Fusion, Culham Laboratory, Abingdon, Oxon.

10-14 10-12 10-10 10-8 10-6 10-4 10-2 100

Sn

Sn-25Li

V

Pb

Li (w/o H3)

100 years10 years1 hour

Decay Heat at the First Wall (W/g)

Idaho National Engineering and Environmental Laboratory

Contact dose (gamma) comparison

From: C.B.A. Forty et. al., Handbook of Fusion Activation Data, Part 1, AEA FUS 180, May 1992 and Part 2, AEA FUS 232,May 1993, AEA Technology Fusion, Culham Laboratory, Abingdon, Oxon. R. Haange et al., “Remote Handling Maintenanceof ITER,” Fusion Energy 1998, Proceedings of the 17th IAEA Fusion Energy Conference, Yokohama, Japan, 18-24 October1998, 3, pgs 965-972

10-14 10-12 10-10 10-8 10-6 10-4 10-2 100 102 104

Sn

Sn-25Li

Pb

Li (w/o H3 )

100 years10 years

Contact Dose at the Shield (Sv/hr)

10CFR835upper limithands-on

1 Sv = 100 Rem

DOE1098-99upper limithands-on

Snowmass-99remote handling

(2628 Sv/lifetime)

R. HaangeRemote Handling

(8 x 109 Sv/lifetime)

Idaho National Engineering and Environmental Laboratory

Vapor pressure comparison

From: The Characterization of High-Temperature Vapors, edited by J.L. Margrave, John Wiley & Sons, Inc. 1967. Sn-25Lidata from R.A. Anderl et al., “Vaporization Properties of Sn-25at%Li Alloy,” Proceedings of the 10th International Conferenceon Fusion Reactor Materials, October 14-19, 2001, Baden-Baden, Germany.

10-9

10-7

10-5

10-3

10-1

400 600 800 1000 1200 1400

SnPbLi25Li-75Sn

Vap

or

Pre

ssu

re (

kPa)

Temperature (C)

Sn-25LiPbLi Sn

Idaho National Engineering and Environmental Laboratory

Radiotoxicity of Liquid Metals

From: C.B.A. Forty et. al., Handbook of Fusion Activation Data, Part 1, AEA FUS 180, May 1992 and Part 2, AEA FUS 232,May 1993, AEA Technology Fusion, Culham Laboratory, Abingdon, Oxon.

Sn

Sn-25Li

Pb

Li (w/o H3) 100 years

1 years

10-6 10-4 10-2 100 102 104 106 108 1010 1012

Specific Activity at the Shield (Bq/kg)

Sn-119m (t1/2

= 0.8 yr)

Ti-204 (t1/2

= 3.8 yr)

Pb-205 (t1/2

= 1.4E7 yr); Bi-207 (t1/2

= 38.0 yr)

Sn-121m (t1/2

= 50.1 yr)

Sn-119m (t1/2

= 0.8 yr)

Sn-121m (t1/2

= 50.1 yr)

Idaho National Engineering and Environmental Laboratory

1

H

3

Li4

Be

11

Na

12

Mg

19

K

20

Ca

21

Sc

22

Ti

23

V

37

Rb

39

Y

40

Zr

41

Nb

55

Cs

56

Ba

57

La

73

Ta

24

Cr

42

Mo

74

W

25

Mn

26

Fe

28

Ni

46

Pd

47

Ag

30

Zn

48

Cd

5

B

31

Ga

49

In

6

C

14

Si

32

Ge

50

Sn

15

P

33

As

8

O

52

Te

9

F

53

I

69

Tm

68

Er

66

Dy

65

Tb

63

Eu

60

Nd

59

Pr

no stable

isotopes

83

Bi

82

Pb

81

Tl

79

Au

77

Ir

no stable

isotopes

70

Yb

72

Hf

27

Co

45

Rh

44

Ru

13

Al

7

N

17

Cl

16

S

29

Cu

34

Se

38

Sr

51

Sb

75

Re

76

Os

78

Pt

80

Hg

58

Ce

6 2

Sm

35

Br

64

Gd

67

Ho

71

Lu

unlimited 10% 1% .1% .01% .001% .0001%

Top half of box: hard spectrum Bottom half of box: soft spectrum

.00001%

Limits on Elements for Class C WasteQualification

From: S.J. Piet, et al., “Initial Integration of Accident Safety, Waste Management, Recycling, Effluent, and MaintenanceConsiderations for Low-Activation Materials”, Fusion Technology, Vol. 19, Jan. 1991, pp. 146-161. Assumes 5 MW/m2 for 4years; and E. T. Cheng, “Concentration Limits of Natural Elements in Low Activation Materials”, presented at ICFRM-8,Sendai, Japan,October 1997

Idaho National Engineering and Environmental Laboratory

Inventory-based radiotoxicity

Metric(Sv) =Σ [Inventory (Ci)*Radiotoxicity(Sv/Ci)]

1.00E-01

1.00E+00

1.00E+01

1.00E+02

1.00E+03

1.00E+04

Gold Tungsten Lead Platinum Palladium Silver

TargetChamber FW

Inventory based Dose Metric (Sv) for Laser IFE

1.00E-01

1.00E+00

1.00E+01

1.00E+02

1.00E+03

1.00E+04

1.00E+05

Gold/Gd Hg Ta Hg/W/Cs Pb/Hf Pb/Ta/Cs

TargetChamber FW

Inventory based Dose Metric (Sv) for Heavy Ion Fusion

Idaho National Engineering and Environmental Laboratory

Aerosol considerations for chamberclearing

• Issues of aerosol generation and transport– Aerosol conservation model– Representative nucleation and growth rates– Particle transport– Particle deposition

• Future work

Idaho National Engineering and Environmental Laboratory

Aerosol conservation model• Evolution of the aerosol size distribution is governed

by the aerosol General Dynamic Equation (GDE):

• This equation demonstrates aerosol particleconservation, where n is the number of particles perunit particle volume per unit gas volume.

( ) ( )∂∂

ν∂∂

∂∂

∂∂

nt

n D n cnnt

nt

ntgrowth growth

+ ∇⋅ − ∇⋅ ∇ + ∇⋅ =

+

+

r r

1 2444444 3444444 1 2444444 3444444Convective Diffusionand Transport

homo hetro coag

Particle Growth andCoagulation

, ,

Idaho National Engineering and Environmental Laboratory

Homogeneous nucleation rate of Pb:

Nucleation rate and critical radius of Pbat various saturation temperatures

Time required to form 1015 Pbparticles/m3

(where coagulation becomes increasinglyimportant)

(these saturation ratios are comparable to thoseachievable in cloud chambers)

10 14

10 16

10 18

10 20

10 22

10 24

10 26

10 28

10 30

10 32

10 34

10 36

10 38

0.01

0.1

1

10

1 10 100

Critical R

adius (nm)

(dashed curves)

HM

G N

ucle

atio

n R

ate

(#/m

3 /s)

(sol

id c

urve

s)

Saturation Ratio

1500 K

2000 K

2500 K

3000 K

1000 K

1500 K

2000 K2500 K

3000 K

3500 K

3500 K

10 -4

10 -2

10 0

10 2

10 4

10 6

0 2 4 6 8 10

Nuc

leat

ion

Tim

e (µ

s)

Saturation Ratio

1500 K

1750 K

2000 K

2500 K

3000 K

Clearing Time (0.1 sec.)

Idaho National Engineering and Environmental Laboratory

Heterogeneous growth and coagulationrate of Pb:Time needed for particles in saturated

vapor to increase volume by 10%Time required for 1 µm dust particles

to change total number by 10%

• Dust particle concentrations generated from homogeneousnucleation are sufficiently large so that particle growth andcoagulation occur faster than chamber clearing times

10 0

10 1

10 2

10 3

10 4

10 5

10 6

0 20 40 60 80 100

Con

dens

atio

n T

ime

(µs)

Saturation Ratio

1500 K

Clearing Time- 0.1 sec.

3500 K

3000 K

2500 K

2000 K

10 -6

10 -5

10 -4

10 -3

10 -2

10 -1

10 0

10 1

10 13 10 14 10 15 10 16 10 17 10 18 10 19 10 20

Tim

e fo

r 10

% C

hang

e (s

ec.)

Initial Number Density (#/m 3)

Clearing Time (0.1 sec.)

Est

imat

ed p

artic

le c

once

ntra

tion

for

hom

ogen

eous

nuc

leat

ion 1000 K

3500 K

Idaho National Engineering and Environmental Laboratory

Homogeneous nucleation rate of W:

Nucleation rate and critical radius of Wat various saturation temperatures

Time required to form 1015 Wparticles/m3

(where coagulation becomes increasinglyimportant)

(these saturation ratios are comparable to thoseachievable in cloud chambers)

10 18

10 20

10 22

10 24

10 26

10 28

10 30

10 32

10 34

10 36

10 38

0.01

0.1

1

10

1 10 100

HM

G N

ucle

atio

n R

ate

(#/s

/m3 )

Critical R

adius (nm)

Saturation Ratio

4000 K

6000 K

7000 K

4500 K

5000 K

3500 K

3500 K

7000 K

(dashed curves)

10 -4

10 -2

10 0

10 2

10 4

10 6

0 2 4 6 8 10

Nuc

leat

ion

Tim

e (µ

s)

Saturation Ratio

4000 K

6000 K

7000 K

4500 K5000 K

3500 K

Clearing Time (0.1 sec)

Idaho National Engineering and Environmental Laboratory

Heterogeneous growth and coagulationrate of W:Time needed for particles in saturated

vapor to increase volume by 10%Time required for 1 µm dust particles

to change total number by 10%

10 0

10 1

10 2

10 3

10 4

10 5

10 6

0 20 40 60 80 100

Con

dens

atio

n T

ime

(µs)

Saturation Ratio

Clearing Time- 0.1 sec.

6000 K

5000 K

4500 K

4000 K

7500 K

10 -6

10 -5

10 -4

10 -3

10 -2

10 -1

10 0

10 1

10 13 10 14 10 15 10 16 10 17 10 18 10 19 10 20

Tim

e fo

r 10

% C

hang

e (s

ec.)

Initial Number Density (#/m 3)

Clearing Time (0.1 sec.)

Est

imat

ed p

artic

le c

once

ntra

tion

for

hom

ogen

eous

nuc

leat

ion 3500 K

7500 K

• Dust particle concentrations generated from homogeneousnucleation are sufficiently large so that particle growth andcoagulation occur faster than chamber clearing times

Idaho National Engineering and Environmental Laboratory

Convective diffusion and transport

• The diffusive transport time constant is• for a characteristic gradient length L = 1 cm and D ~ 10-5

m2/s, τdiff = 10 s. This value decreases when particle slipis considered.

• Migration velocities for gravitational settling, electrostaticmobility, and thermophoretic forces yield time constantsτmigration ~ L/Ci ~ 1 - 10 s.

• These mechanisms are of less importance for inter-shotaerosol transport than for long-term transport associatedwith accident analysis

τdiffLD=

2

∂n

∂t + ∇ • nv v ( ) − ∇ • D∇n( ) + ∇ •v c n

Idaho National Engineering and Environmental Laboratory

Particle deposition

• Deposition via diffusive and/or migratory transport ofparticles are secondary effects for inter-shot aerosoltransport

• inertial deposition and turbulent deposition are importantfor inter-shot aerosol transport because they areresponsible for placing particles at undesired locations,such as on final optics or in ducts.

r J

wall= −D∇n +

r c migration +

r c inertial +

r c turbulent( )n

Idaho National Engineering and Environmental Laboratory

Future work for aerosol formation• Aerosol model requires local state properties (T,P) for

determining nucleation and growth rates. Flow fieldis also needed for particle convection and deposition

• Solve within Hydrodynamic Chamber Model• Modify existing INEEL fluids/aerosol model to

simulate a dry-wall IFE chamber for the purpose ofscoping studies

• Experimental benchmarking