Title: Depleted Uranium DU: More than you want to know . . . But what every health physicist ought to know
1Depleted Uranium (DU)More than you want to
know . . . But what every health physicist
ought to know
Ronald L. Kathren, CHP Professor
Emeritus Washington State University at
Tri-Cities Presented at a breakfast meeting
of the Columbia Chapter of the Health Physics
Society Richland, WA November 15, 2007 (at the
ungodly hour of 7 AM!)
2Historical and General Introduction
- Human experience with uranium goes back two
millennia the Romans used uranium oxide to
impart a yellow color to ceramic glazes - At least as early as the 1400s, pitchblende,
extracted from the Joachimsthal mines, was used
to color glass - Uranium was discovered by German chemist Martin
Klaproth in 1789 named after planet Uranus
3Natural Uranium
- A dense (? 18.68 g cm-3), silvery white weakly
radioactive and chemically toxic heavy metal - Ubiquitous in the environment (heaviest natural
element) - NatU contains Three isotopes
- U-238 99.27 wt 50 of activity
- U-235 0.72 wt
- U-234 0.0057 wt 50 of
activity - Several valence states (4, 5, 6) compounds
range from soluble (UF6, UCl4) to insoluble
(typically oxides UO2, UO3, UO4, U3O8 - Pyrophoric particulates oxidize quickly in air
4More History
- Uranium metal isolated in 1841 by French chemist
Eugene-Melchior Peligot - Radioactivity of uranium was discovered in March
1896 by French physicist Henri Becquerel - Fission of U discovered in 1939 by German
chemists Otto Hahn and Fritz Strassmann process
explained by physicists in exile Lise Meitner and
Otto Frisch
5Toxicological Studies
- First toxicological studies by chemist Christian
Gmelin (1824) concluded that uranium was a
feeble poison - Gmelins work confirmed by other researchers over
the next several decades - Since about 1860 until discovery of insulin in
1920s used therapeutically to treat diabetes
mellitus
6Toxicological Studies II
- Extensive studies of U toxicity in Manhattan
District confirmed low level of toxicity - Low order of toxicity further butressed by
studies of accidental exposures and epidemiologic
studies of U workers - Use of DU in Gulf Wars and Kosovo generated new
interest and intensive study but many questions
still remain
7Production of Depleted Uranium
- A byproduct of the enrichment process
- Two basic methods
- Gaseous diffusion
- Gas centrifugation
- U-235 content reduced to 0.2 wt
- Specific activity about 60 of NatU
- 88.8 of activity from 238U, 9.9 from 234U
- and only 1.1 from 235U
8Radiological Characteristics of DU
9Uses of Depleted Uranium
- Pigments
- Industrial catalyst
- Counterweight for aircraft control surfaces
- Ballast for ships
- Radiation shielding
- Munitions
- Armor
10Munitions Usage
- High density and self sharpening characteristics
provide excellent armor piercing capability - High density and strength also make it excellent
for tank armor - DU penetrators produce airborne particulates of
typically high fired and hence insoluble DU which
fall out close to the point of impact and produce
localized ground contamination
11Toxicokinetics
- Oral absorption poor few per cent
- Percutaneous absorption has not been observed in
humans - Absorption following inhalation a function of
solubility, particle size ICRP lung model
applies - Approximately 70 of absorbed U is excreted in
first 24 hours, largely via urine
12Biokinetic Models for Uranium
- Several biokinetic models for U have been
proposed over last 50 years - ICRP Publication 69 (1995) likely most generally
used and accepted model - Other models have been proposed in general are
similar to and basically refinements of ICRP
model - Models may not fit well solubility, route of
intake are important factors
13Inhaled Uranium
- Rely on ICRP lung model
- Type F Compounds UF6, UO2F, UO2(NO3)2 100
absorption of fraction not excreted via GI tract
with half time of 10 min - Type M Compounds (UO3, UF4, UCl4, U3O8) 10
absorption of fraction not excreted via GI tract
with half time of 10 min remaining 90 of
nonexcreted fraction has half time of 140 days - Type S Compounds (UO2, U3O8) low and slow
absorption of the fraction not cleared via GI
tract, 99.9 absorbed via respiratory tract with
half life of 7000 days ( 19 years) - Note Some compounds such as U3O8 may behave as
Class M or Class S under specific circumstances
14Ingested Uranium
- Gut absorption poor f1 1-2 for soluble U,
order of magnitude less for insoluble forms - ICRP uses 0.02 for soluble forms and 0.002 for
highly insoluble forms, the latter specified as
UO2 and U3O8. - Gut absorption may be affected by food
15Percutaneous Absorption
- Not likely no evidence to support transfer
through unbroken human skin - May enter blood through cuts and abrasions
- Depositions in wounds may remain for years,
slowly releasing U and progeny into systemic
circulation kidney concentration - builds up with time
16Absorption and Distribution
- Once absorbed into systemic circulation, most U
is quickly excreted via the kidneys - Small fractions are deposited in skeleton, liver
and kidney - Depots may have both long and short term
residence compartments
17Bioassay for DU
- Fecal analysis useful for inhaled material,
especially after acute accidental intake - In vivo counting useful reasonable LLD (few mg)
for lung counts - Urinalysis (KPA, ICPMS) most practical and has
excellent sensitivity - Hair analysis not established technique and
subject to interferences and error - Blood concentration insufficiently sensitive and
may not be practical
18Chemical Toxicity
- U is a heavy metal and exhibits heavy metal
toxicity - Low enrichment U ( 15 U-235) is primarily
chemically toxic - Toxic effects (including death) have been clearly
demonstrated in animals but not in humans
sensitivity variable among species
19LD50
- Variable depending on animal species humans seem
to have lower sensitivity to U toxicity than
animals - No data for humans, but limited human data and
extrapolation from animals suggests that the
acute LD50 for ingested or inhaled U is at least
several grams
20Hard to Believe but True
- There has never been a documented death
attributable to U ingestion or inhalation in
humans - BUT . . . This does not mean that DU is
without toxic effects . . . - More study of DU and its possible effects in man
is clearly indicated
21Chemotoxic Effects Kidney
- Kidney is the most sensitive organ for chemotoxic
effect of DU - Histopathology and apparent mild functional
changes may occur days after large acute intakes
(tens to hundreds of mg) and manifest as injury
to renal tubular epithelial cells - Biomarkers of tubular effects include glucosuria,
enzymuria, albuminuria, and elevated blood
creatinine or NPN/BUN.
22Chemotoxic Effects Kidney
- Threshold for renal effects from acute exposure
likely 2 µg U/g kidney but 3 µg U/g generally
accpted as of now - Effects are typically transient but are more
serious and longer lasting with higher exposures - Studies of chronic occupational exposure in
workers and Gulf War veterans suggests
concentrations 1µg/g kidney may produce mild
tubular dysfunction (Thun et al. 1985 Squibb et
al. 2005).
23Chemotoxic Effects
- Effects on other systems -- CNS, cardiovascular,
ocular, liver, immune system -- typically not
observed in animal studies or in humans, but any
such effects may have been overshadowed and
masked by far more severe renal effects - No evidence of reproductive system dysfunction or
sperm abnormalities in male Gulf War veterans,
nor any evidence of excess fetal abnormalities or
mortality. Placental transfer equivocal
24Chemical Genotoxicity
- Has not been seen (or even looked for) in animal
studies - A 10 y followup study of Gulf War veterans
classified as high exposure based on urine
biomarkers was equivocal (McDiarmid et al. 2004) - Recent in vitro studies with Chinese hamster
cells suggests chromosome breakage and
mutagenicity associated with heavy metals
including U (Stearns et al 2005) but such studies
have not been confirmed nor are they necessarily
applicable to human exposures
25Radiation from DU
- All three U isotopes in DU are alpha emitters
(plus associated photons) - Specific activity of DU 14.9 kBq g-1
- (4.1 x 10-7 Ci g-1 )
- Decay chain products emit betas, photons
- Surface dose rate from infinite slab of DU is
2.55 mGy h-1, 90 from beta and 10 from photons
26External Exposure Considerations
- Potential for significant external exposure is
small to zero - Dose rate 10 cm from an infinite slab of DU is
only 0.1 mGy h-1 - Unless DU is in contact with the skin (or very
nearly so) it is virtually impossible to get a
dose sufficient to produce any deterministic
effect
27Internal Exposure Considerations
- Risk of deterministic effects from radiation
virtually zero as chemotoxicity effects would be
overwhelming and possibly fatal irrespective of
route of entry - Ditto for carcinogenic risks from ingestion of
soluble DU ingestion of 1 g of soluble DU
produces a total stochastic risk of 3.3 x 10-5
including both carcinogenesis and genetic
effects.
28Risk from Inhaled DU
- Inhalation of soluble DU compounds dose not pose
significant stochastic or deterministic risk from
radiation the chemical effects are overwhelming - Inhalation of insoluble aerosols may pose
significant stochastic risk e.g. inhalation of
1 mg of a 1 µm AMAD Class S aerosol produces a
lifetime stochastic risk of 5.6 x 10-6 primarily
from lung cancer - Lung cancer risk may be potentiated or increased
by other insults such as smoking
29Epidemiology
- Numerous radioepidemiologic studies have been
done over the past three decades of uranium
miners, millers, and workers and of populations
exposed to high background levels of U - DU studies are under way in military and civilian
populations in areas where DU munitions were used
30Epidemiologic Findings
- Results are at most equivocal and certainly
comforting no study has shown a statistically
significant excess for total cancer (so if there
are in fact effects they will be minimal) - No study has shown long term kidney or other
somatic effects associated with acute or chronic
exposure to uranium