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Technical Factsheet on: CADMIUM
List of Contaminants
As part of the Drinking Water and Health pages, this fact sheet is part of a larger publication:
National Primary Drinking Water Regulations
Drinking Water Standards
MCLG: 0.005 mg/l
MCL: 0.005 mg/l
HAL(child): 1- to 10-day: 0.04 mg/L; Longer-term: 0.005 mg/L
Health Effects Summary
Acute: EPA has found cadmium to potentially cause a variety of effects from acute exposures,
including: nausea, vomiting, diarrhea, muscle cramps, salivation, sensory disturbances, liver
injury, convulsions, shock and renal failure.
Drinking water levels which are considered "safe" for short-term exposures: For a 10-kg (22 lb.)
child consuming 1 liter of water per day, a one- to ten-day exposure to 0.04 mg/L; a longer-term
(up to 7 years) exposure to 0.005 mg/L.
Chronic: Cadmium has the potential to cause kidney, liver, bone and blood damage from long-
term exposure at levels above the MCL.
Cancer: There is inadequate evidence to state whether or not cadmium has the potential to cause
cancer from lifetime exposures in drinking water.
Usage Patterns
2.9 million lbs of cadmium were produced in the US in 1986, and nearly twice that amount was
imported in the same year.
According to 1986 estimates, cadmium is used primarily for metal plating and coating operations
(35%), including transportation equipment, machinery and baking enamels, photography,
television phosphors. It is also used in nickel-cadmium and solar batteries (25%), in pigments
(20%), as a stabilizer in plastics and synthetic products (15%), alloys and other uses (5%).
Cadmium salts have had a very limited use as fungicide for golf courses and home lawns.
Release Patterns
Cadmium occurs naturally in zinc, lead and copper ores, in coal and other fossil fuels, shales and
is released during volcanic action. These deposits can serve as sources to ground and surface
waters, especially when in contact with soft, acidic waters.
Major industrial releases of cadmium are due to wastestreams and leaching of landfills, and from
a variety of operations that involve cadmium or zinc. These may include: during the smelting and
refining of zinc, lead and copper bearing ores; during recovery of metal by processing scrap;
during melting and pouring of cadmium metal; during casting of various cadmium alloy products
used for coating telephone cables, trolley wires, welding, electrodes, automatic sprinkling
systems, steam boilers, fire alarms, high pressure/temperature bearings, starting switches, aircraft
relays, light duty circuit breakers, low temperature solder, and jewelry; during fabrication of
metal, alloys, or plated steel; during casting and use of solders; during melting of cadmium
ingots for paint and pigment manufacture used for coloring of plastics and ceramic glazes,
electroplating, and in chemical synthesis; during coating of metals by hot dipping or spraying;
during manufacture of nickel-cadmium batteries for use in radio portable telephones,
convenience appliances, and vented cells used in airplanes, helicopters, and stand-by power and
lighting. The remaining cadmium emissions are from fossil fuel combustion, fertilizer
application, and sewage sludge disposal.
Cadmium also occurs as a by-product of corrosion of some galvanized plumbing and distribution
system materials.
From 1987 to 1993, according to EPA's Toxic Chemical Release Inventory, cadmium releases
were primarily from zinc, lead and copper smelting and refining industries, with the largest
releases occurring in Arizona and Utah.
Environmental Fate
The oxide and sulfide are relatively insoluble while the chloride and sulfate salts are soluble. The
adsorption of cadmium onto soils and silicon or aluminum oxides is strongly pH-dependent,
increasing as conditions become more alkaline. When the pH is below 6-7, cadmium is desorbed
from these materials. Cadmium has considerably less affinity for the absorbents tested than do
copper, zinc, and lead and might be expected to be more mobile in the environment than these
materials.
Studies have indicated that cadmium concentrations in bed sediments are generally at least an
order of magnitude higher than in overlying water. A study of Ottawa River sediments found that
sediment composed mainly of well sorted sand may be an efficient sink for heavy metals if there
is a significant amount of organic material added to the sediments by the commercial activities
such as logging. Both sorption and desorption were controlled by the nature of total heavy metal
loading, the sediment type, and the surface water characteristics.
Addition of anions, such as humate, tartrate, to dissolved cadmium caused an increase in
adsorption. The mode by which cadmium is sorbed to the sediments is important in determining
its disposition toward remobilization.
Cadmium found in association with carbonate minerals, precipitated as stable solid compounds,
or co-precipitated with hydrous iron oxides would be less likely to be mobilized by resuspension
of sediments or biological activity. Cadmium absorbed to mineral surfaces (eg clay) or organic
materials would be more easily bioaccumulated or released in the dissolved state when sediments
are disturbed, such as during flooding.
Cadmium is not known to form volatile compounds in the aquatic environment.
Bioconcentration of cadmium sulfate, nitrate and chloride has been studied in a wide variety of
aquatic organisms, and can be quite high in some species, low in others. For example, rainbow
trout have a BCF of 33 while a BCF of 2213 was measured in the mosquito fish. Similarly,
different species of clams have BCFs ranging from 160 to 3770.
Chemical/Physical Properties
CAS Number: 7440-43-9 (metal)
Color/ Form/Odor: Cadmium is a lustrous silvery metallic element found only
in combined forms in nature.
Soil sorption coefficient: Koc = N/A; mobility higher than other metals
Bioconcentration Factor: Fish: 33 to 2213; Shell fish: 5 to 2500; Other
invertebrates: 164 to 4190; Plants: 603 to 960.
Common Ores: sulfide- greenockite; carbonate- octavite; others: hawleyite.
Also found in zinc, copper, lead ores.
Solubilities (water):
acetate- very soluble
bromide- 570 g/L at 10 deg C
carbonate- insoluble
chloride- 1400 g/L at 20 deg C
fluoroborate- very soluble
mercury sulfide- N/A
nitrate- 1090 g/L at 0 deg C
oxide- insoluble
sulfate- 755 g/L at 0 deg C
sulfide- insoluble
stearate- N/A
Other Regulatory Information
Monitoring:
-- For Ground Water Sources:
Initial Frequency-1 sample once every 3 years
Repeat Frequency-If no detections for 3 rounds, once every 9 years
-- For Surface Water Sources:
Initial Frequency-1 sample annually
Repeat Frequency-If no detections for 3 rounds, once every 9 years
-- Triggers - If detect at > 0.005 mg/L, sample quarterly.
Analysis
| Reference Source | Method Number |
| EPA 600/4-79-020 | 213.2 |
| NTIS PB 91-231498 | 200.7 |
| Standard Methods | 3113B |
Treatment/Best Available Technologies: Coagulation/Filtration, Ion Exchange, Lime
Softening, Reverse Osmosis
Toxic Release Inventory - Releases to Water and Land, 1987 to 1993 (in pounds):
| | Water | Land |
| TOTALS | 31,487 | 2,059,574 |
| Top Seven States * |
|---|
|
AZ | 503 | 433,035
| |
UT | 1,750 | 372,010
| |
MT | 0 | 315,965
| |
TN | 2,700 | 288,781
| |
ID | 250 | 225,761
| |
MO | 2,361 | 189,914
| |
WI | 0 | 106,000
|
| Major Industries* |
|---|
|
Zinc, lead smelting | 5,061 | 831,948
| |
Copper smelting, refining | 2,253 | 805,045
| |
Indust. inorganic chems | 250 | 225,761
| |
Electroplating, anodizing | 0 | 106,000
| |
Steelworks, blast furnaces | 5 | 13,000
| |
Inorganic pigments | 5,140 | 7,000
|
* State/Industry totals only include facilities with releases greater than a certain amount - usually
1000 to 10,000 lbs.
For Additional Information:
EPA can provide further regulatory and other general information:
EPA Safe Drinking Water Hotline - 800/426-4791
Other sources of toxicological and environmental fate data include:
Toxic Substance Control Act Information Line - 202/554-1404
Toxics Release Inventory, National Library of Medicine - 301/496-6531
Agency for Toxic Substances and Disease Registry - 404/639-6000
List of Contaminants
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