CADMIUM

Cadmium was discovered in 1817 by a physician, Friedrich Stromeyer (1776-1835). The element was first found in the condensation of vapors (mixed with soot and zinc oxides) that rose out of a furnace in which zinc oxide was being roasted. Cadmium’s discovery is also loosely attributed to K.S.L. Hermann and J.C.H. Roloff who may have found cadmium in zinc oxide during the same year. A historical debate still remains as to who actually discovered the pure form of the element first.
The phase of scientific history in which Stromeyer was active was one in which chemical discovery was being accomplished primarily by pharmacists, apothecaries and physicians. The practice of alchemy was dying out, and chemistry was just beginning to emerge as a separate science. Stromeyer, a professor at the University of Göttingen, was testing zinc oxide, a medicine in those days, for purity.

Cadmium is a grey-white, soft, blue-white malleable, lustrous metal. It is insoluble in cold water, hot water, methanol, diethyl ether, and n-octanol. It is stable and incompatible with strong oxidising agents, nitrates, nitric acid, selenium, and zinc, and the powdered metal may be pyrophoric and flammable.

Cadmium is associated with occupations such as industrial processes, metal plating, and production of nickel– cadmium batteries, pigments, plastics, and other synthetics. Cadmium metal is produced as a by-product from the extraction, smelting, and refining of the non-ferrous metals zinc, lead, and copper. In view of the unique properties, cadmium metal and cadmium compounds are used as pigments, stabilisers, coatings, specialty alloys, and electronic compounds.

Elemental cadmium has a hexagonal crystal structure. Cadmium is a silver-white metal, malleable and ductile, but at 80 C becomes brittle. It remains lustrous in dry air and is only slightly tarnished by air or H2O at standard conditions. The element may be sublimed in a vacuum at a temperature of about 300 C, and when heated in air burns to form the oxide. Cadmium dissolves slowly in hot dilute HCl or H2SO4 and more readily in HNO3. Naturally occurring isotopes 106, 108, 110 114, 116. 113Cd is unstable with respect to beta decay (0.3 MeV) into 113In (t1/2 1013 years).
In virtually all of its compounds, cadmium exhibits the +2 oxidation state, although compounds of cadmium(I) containing the ionCd2 2+, have occasionally been reported. Cadmium hydroxide is more basic than zinc hydroxide, and only slightly amphiprotic, requiring very strong alkali to dissolve it, and forming Cd(OH)3 or Cd(OH)4 2 depending upon the pH.

Calmium is an odorless, silver-white lustrous metal with a bluish tinge, which is ductile and highly malleable with a melting point of 321 °C. The metal is soft enough to cut with a knife and will tarnish in air; as a powder, cadmium is flammable. Burning cadmium results in an odorless yellowbrown cadmium fume (cadmium monoxide or cadmium oxide fume) composed of finely divided particles dispersed in air. Both cadmium and cadmium oxide are insoluble in water and have a vapor pressure of approximately 0 mmHg. Cadmium is insoluble in water but can be solubilized in acid. Cadmium salts (e.g., cadmium sulfate and cadmium chloride) are soluble in water.

Cadmium is a soft, blue-white metal that is malleable and ductile although it becomesbrittle at about 80°C. It is also found as a grayish-white powder. It is considered rare and isseldom found by itself as an ore. Its melting point at 320.9°C is considered low. Its boilingpoint is 765°C, and its density is 8.65 g/cm³. Certain alloys of cadmium have extremely lowmelting points at about 70°C.

There are 52 isotopes of cadmium. Forty-four are radioactive and artificiallyproduced, ranging from Cd-96 to Cd-131. Of these 52 isotopes, there are five stableisotopes plus three naturally occurring radioactive isotopes with extremely long half-livesthat are considered as contributing to the element’s natural occurrence in the Earth’scrust. The three naturally radioactive isotopes (Cd-106, Cd-113, and Cd-116) are thelongest known beta emitters. They are two million years older than when the solar systemwas formed about 4.5 billion years ago. The five stable isotopes and their proportionalcontributions to the element’s existence on Earth are as follows: Cd-108 = 0.89%,Cd-110 = 12.49%, Cd-111= 12.80%, Cd-112 = 24.13%, and Cd-114 = 28.73%.

The word cadmium is from the Latin word cadmia or the Greek word kadmeia, meaning the zinc oxide ore “calamine” that contains the element cadmium.

Cadmium is considered a rare element even though it is widely distributed over the Earth’scrust. Its estimated abundance in the Earth’s crust is 1.10^-1 milligrams per kilogram. It is consideredthe 65th most abundant element, but it does not occur as a free metal in nature. It isusually found in relationship with other metallic ores. Its abundance is only about 1/1000ththat of zinc. It is found in an ore called greenockite, which is cadmium sulfite (CdS). This oredoes not have a high enough concentration of cadmium to be mined profitably. Cadmiumis found along with zinc, lead, and copper ores. Today, most cadmium is obtained as a byproductfrom the processing and refining of zinc ores. In addition, dust and fumes from roastingzinc ores are collected by an electrostatic precipitator and mixed with carbon (coke) andsodium or zinc chloride. This residue is then treated to recover the cadmium. Other refiningprocesses can obtain up to 40% recovery of cadmium from zinc ores.
Greenockite ore, as well as zinc and other ores, which produce cadmium as a by-product,are found in many countries, including Australia, Mexico, Peru, Zaire, Canada, Korea, andBelgium-Luxembourg and in the central and western United States.

Although cadmium is not considered a transition element in some periodic tables, it is thecentral element of the triad with zinc and mercury. Zinc is just above it and mercury is below itin group 12 of the periodic table. Cadmium’s chemical and physical properties are similar to itsgroup 12 mates. Their electronegativity is very similar: Zn = 1.6, Cd = 1.7, and Hg = 1.9.
Cadmium is resistant to alkalis, but is soluble in acids, mainly nitric acid. Although it isused to electroplate steel to prevent corrosion, it will tarnish in moist air.

Cadmium was discovered by Stromeyer in 1817 from an impurity in zinc carbonate. Cadmium most often occurs in small quantities associated with zinc ores, such as sphalerite (ZnS). Greenockite (CdS) is the only mineral of any consequence bearing cadmium. Almost all cadmium is obtained as a by-product in the treatment of zinc, copper, and lead ores. Cadmium is a soft, bluish-white metal which is easily cut with a knife. It is similar in many respects to zinc. It is a component of some of the lowest melting alloys; it is used in bearing alloys with low coefficients of friction and great resistance to fatigue; it is used extensively in electroplating, which accounts for about 60% of its use. Cadmium is also used in many types of solder, for standard E.M.F. cells, for Ni-Cd batteries, and as a barrier to control atomic fission. The market for Ni- Cd batteries is expected to grow significantly. Cadmium compounds are used in black and white television phosphors and in blue and green phosphors for color TV tubes. It forms a number of salts, of which the sulfate is most common; the sulfide is used as a yellow pigment. Cadmium and solutions of its compounds are toxic. Failure to appreciate the toxic properties of cadmium may cause workers to be unwittingly exposed to dangerous fumes. Some silver solders, for example, contain cadmium and should be handled with care. Serious toxicity problems have been found from long-term exposure and work with cadmium plating baths. Cadmium is present in certain phosphate rocks. This has raised concerns that the long-term use of certain phosphate fertilizers might pose a health hazard from levels of cadmium that might enter the food chain. In 1927 the International Conference on Weights and Measures redefined the meter in terms of the wavelength of the red cadmium spectral line (i.e., 1 m = 1,553,164.13 wavelengths). This definition has been changed (see under Krypton). The current price of cadmium is about 50￠/g (99.5%). It is available in high purity form for about $550/kg. Natural cadmium is made of eight isotopes. Thirty-four other isotopes and isomers are now known and recognized.

Batteries, including Ni-Cd storage batteries; coating and electroplating steel and cast iron; pigments; plastic stabilizers; constituent of low melting or easily fusible alloys, e.g., Lichtenberg's, Abel's, Lipowitz', Newton's, and Wood's metal; electronics and optics; soft solder and solder for aluminum; reactor control rods; hardener for copper; catalytsts.

cadmium is highly toxic elements. Cadmium can often be found in batteries.cadmium form the corresponding oxide when heated under oxygen. cadmium follow the general formula MX₂ and are either insoluble (X=F) in water or show a low aqueous solubility.

Cadmium alloyed with silver forms a type of solder with a low melting point. It is used tojoin electrical junctions and other specialized metallic components. Precautions are required since it is a toxic substance. (Note: This is not the same as common solder used to join metals,which is relatively safe.) Other cadmium alloys are used to manufacture long-wearing bearingsand as thin coatings for steel to prevent corrosion.
Cadmium is a neutron absorber, making it useful as control rods in nuclear reactors. Therods are raised to activate the reactor and then lowered into the reactor to absorb neutronsthat halt the fission reaction.Cadmium, along with nickel, forms a nickel-cadmium alloy used to manufacture “nicadbatteries” that are shaped the same as regular small dry-cell batteries.
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Cadmium is used in electroplating, in nickelcadmiumstorage batteries, as a coating forother metals, in bearing and low-meltingalloys, and as control rods in nuclear reactors.Cadmium compounds have numerousapplications, including dyeing and printingtextiles, as TV phosphors, as pigments andenamels, and in semiconductors and solarcells.
Vegetables and cereals are the main sourcesof dietary Cd while meat and fish contain themetal to a lesser extent.
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A soft bluish metal, cadmium is extremely toxic, particularly in the compounds used for photography. It is found in zinc ores and in the mineral greenockite (CdS).

Cadmium often produces together with Zinc (Zn). The first output part is gathered at the distillation, using the lower boiling point of Cd than that of Zn. Redistillation purifies the material. The Czochralski and horizontal Stockbarger methods are used to grow a single crystal, after melting has taken place.
Thin films are deposited by vacuum evaporation using direct heating in a conical, basket-type heater made of chromel, Nb, Ta, W, Ni, or Fe, or in a Mo or Ta boat. External heating of an alumina crucible with a W heater is also possible. It is also possible to heat an iron crucible externally using a nichrome heater. The evaporation rate at 264 ℃ (sublimation) is 2.67×10^-4 g/cm² s.

Two major processes are used for producing cadmium: (1) pyro-hydro-metallurgical and (2) electrolytic. Zinc blende is roasted to eliminate sulfur and to produce a zinc oxide calcine. The latter is the starting material for both processes. In the pyro-hydro-metallurgical process, the zinc oxide calcine is mixed with coal, pelletized, and sintered. This procedure removes volatile elements such as lead, arsenic, and the desired cadmium. From 92 94% of the cadmium is removed in this manner, the vapors being condensed and collected in an electrostatic precipitator. The fumes are leached in H2SO4 to which iron sulfate is added to control the arsenic content. The slurry then is oxidized, normally with sodium chlorate, after which it is neutralized with zinc oxide and filtered. The cake goes to a lead smelter, while the filtrate is charged with highpurity zinc dust to form zinc sulfate or zinc carbonate and cadmium sponge. The latter is briquetted to remove excess H2O and melted under caustic to remove any zinc. The molten metal then is treated with zinc ammonium chloride to remove thallium, after which it is cast into various cadmium metal shapes. The process just described is known as the melting under caustic process. In a distillation process, regular rather than high-purity zinc is used to make the sponge. Then, after washing and centrifuging to remove excess H2O, the sponge is charged to a retort. The heating and distillation process is under a reducing atmosphere. Lead and zinc present in the vapors contaminate about the last 15% of the distillate. Thus, a redistillation is required. The cadmium vapors produced are collected and handled as previously described.

cadmium: Symbol Cd. A soft bluishmetal belonging to group 12 (formerlyIIB) of the periodic table; a.n.48; r.a.m. 112.41; r.d. 8.65; m.p.320.9°C; b.p. 765°C. The element’sname is derived from the ancientname for calamine, zinc carbonateZnCO₃, and it is usually found associatedwith zinc ores, such as sphalerite(ZnS), but does occur as themineral greenockite (CdS). Cadmiumis usually produced as an associateproduct when zinc, copper, and leadores are reduced. Cadmium is used inlow-melting-point alloys to make solders,in Ni–Cd batteries, in bearingalloys, and in electroplating (over50%). Cadmium compounds are usedas phosphorescent coatings in TVtubes. Cadmium and its compoundsare extremely toxic at low concentrations;great care is essential wheresolders are used or where fumes areemitted. It has similar chemical propertiesto zinc but shows a greater tendencytowards complex formation.The element was discovered in 1817by F. Stromeyer.

Silver-white blue tinged lustrous metallic solid.

The finely divided metal is pyrophoric. Slowly oxidized by moist air to form CADMIUM oxide. Insoluble in water.

A violent explosion occurred 30 minutes after placement of a CADMIUM rod into hydrazoic acid [Mellor 8 Supp. 2:50 1967]. Fused ammonium nitrate with powdered metal often produces a violent explosive reaction. Reactivity similar to zinc. May be incompatible with oxidants.

Cadmium powder, dust, and fumes are all flammable and toxic if inhaled or ingested.Cadmium and many of its compounds are carcinogenic.
Severe illness and death can occur from exposure to many cadmium compounds. It isabsorbed in the gastrointestinal tract. However, it can be eliminated in the urine and fecesin young, healthy people.

There are several reports of cadmium poisoningand human death. Cadmium can enterthe body by inhalation of its dusts or fumes,or by ingestion. In humans the acute toxicsymptoms are nausea, vomiting, diarrhea,headache, abdominal pain, muscular ache,salivation, and shock. In addition, inhalationof its fumes or dusts can cause cough,tightness of chest, respiratory distress, congestionin lungs, and bronchopneumonia. A30-minute exposure to about 50 mg/m³ of itsfumes or dusts can be fatal to humans. Theoral LD₅₀ value in rats is within the range of250 mg/kg.
Cadmium is a poison that is accumulatedin the liver and kidneys. Thus, chronicpoisoning leads to liver and kidney damage.It is very slowly excreted. Its biologicalhalf-life in humans is estimated atabout 20–30 years (Manahan 1989). Cadmiumlevel in the kidney at 200 μg/g,can damage proximal tubules, resulting intheir inability to reabsorb small-moleculeproteins, such as β₂-microglobulin (Luand Kacey 2003). Cigarette smoking andcalcium-deficient diet enhance its toxicity.Renal toxicity may occur in human subjectsas a result of chronic ingestion of low-leveldietary Cd. The absorption of this metal,however, through the GI tract is low. Cadmiumis also known to produce the so-calleditai-itai disease, which is a chronic renaldisease, producing bone deformity and kidneymalfunction. Cadmium, similar to otherheavy meals, binds to the sulfhydryl (-SH)groups in enzymes, thus inhibiting enzymaticacitivity. Intramuscular administrationof cadmium produced tumors in the lungs and blood in rats. There is sufficient evidenceof its carcinogenicity in animals.
Data on accumulation of Cd in human kidneyand liver have been reviewed by Sataruget al. (2000). Epidemiological and autopsystudies have shown a relationship betweenthe tubular dysfunction and kidney Cd burden.A maximum tolerable level of kidneyCd has been suggested as 50 μg/g (wetweight) corresponding to a urinary excretionof 2 μg Cd per day. Safe daily levels of Cdintake in humans have been recommended tobe kept below 30 μg per day.

Flammable in powder form. Combustible.

core: cadmium
reagent type: catalyst

Cadmium (symbol Cd) is a silvery-white crystallinemetal that has a specific gravity of 8.6,is very ductile, and can be rolled or beaten intothin sheets. It resembles tin and gives the samecharacteristic cry when bent, but is harder thantin. A small addition of zinc makes it very brittle.It melts at 320°C and boils at 765°C. Cadmiumis employed as an alloying element insoft solders and in fusible alloys, for hardeningcopper, as a white corrosion-resistant platingmetal, and in its compounds for pigments andchemicals. It is also used for Ni–Cd batteriesand to shield against neutrons in atomic equipment;but gamma rays are emitted when theneutrons are absorbed, and these rays requirean additional shielding of lead.
Most of the consumption of cadmium is forelectroplating. For a corrosion-resistant coatingfor iron or steel a cadmium plate of 0.008 mmis equal in effect to a zinc coat of 0.025 mm.The plated metal has a silvery-white color witha bluish tinge, is denser than zinc, and harderthan tin, but electroplated coatings are subjectto H2 embrittlement, and aircraft parts are usuallycoated by the vacuum process. Cadmiumplating is not normally used on copper or brasssince copper is electronegative to it, but whenthese metals are employed next to cadmium-plated steel a plate of cadmium may beused on the copper to lessen deterioration.

Confirmed human carcinogen with experimental carcinogenic, tumorigenic, and neoplastigenic data. A human poison by inhalation and possibly other routes. Poison experimentally by ingestion, inhalation, intraperitoneal,

Cadmium is a highly corrosion resistant and is used as a protective coating for iron, steel, and copper; it is generally applied by electroplating, but hot dipping and spraying are possible. Cadmium may be alloyed with copper, nickel, gold, silver, bismuth, and aluminum to form easily fusible compounds. These alloys may be used as coatings for other materials; welding electrodes, solders, etc. It is also utilized in electrodes of alkaline storage batteries, as a neutron absorber in nuclear reactors, a stabilizer for polyvinyl chloride plastics, a deoxidizer in nickel plating; an amalgam in dentistry; in the manufacture of fluorescent lamps, semiconductors,photocells, and jewelry, in process engraving, in the automobile and aircraft industries; and to charge Jones reductors. Various cadmium compounds find use as fungicides, insecticides, nematocides, polymerization catalysts, pigments, paints, and glass; they are used in the photographic industry and in glazes. Cadmium is also a contaminant of superphosphate fertilizers. Human exposure to cadmium and certain cadmium compounds occurs through inhalation and ingestion. The entire population is exposed to low levels of cadmium in the diet because of the entry of cadmium into the food chain as a result of its natural occurrence. Tobacco smokers are exposed to an estimated 17 μg/cigarette. Cadmium is present in relatively low amounts in the earth’s crust; as a component of zinc ores, cadmium may be released into the environment around smelters

If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Seek medical attention immediately. Ifthis chemical has been inhaled, remove from exposure,begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medical attention. Give large quantities of water and inducevomiting. Do not make an unconscious person vomit.Medical observation is recommended for 24-48 h afterbreathing overexposure, as pulmonary edema may bedelayed. As first aid for pulmonary edema, a doctor orauthorized paramedic may consider administering a corticosteroid spray.Note to physician: For severe poisoning do not use BAL[British Anti-Lewisite, dimercaprol, dithiopropanol(C3H8OS2)] as it is contraindicated or ineffective inpoisoning from cadmium.

Cadmium and cadmium compounds are known to be human carcinogens based on sufficient evidence of carcinogenicity from studies in humans, including epidemiological and mechanistic studies. Cadmium and cadmium compounds were first listed as reasonably anticipated to be human carcinogens in the First Annual Report on Carcinogens in 1980, based on sufficient evidence of carcinogenicity from studies in experimental animals. The listing was revised to known to be human carcinogens in the Ninth Report on Carcinogens in 2000.

Cadmium inhibits plasma membrane calcium channels and Ca2t-ATPases. It also inhibits repair of DNA damaged by various chemicals, an effect which is believed to be associated with the induction of tumors. Although cadmium forms a metallothionein, the preformed cadmium metallothionein is nephrotoxic (toxic to the kidneys); it is suggested that effects occur when, at some stage in the kidney, the cadmium is dissociated from the metallothionein. In Itai-Itai disease (see Human under Chronic Toxicity section), patients were found to have chromosome abnormalities.
Cadmium has an affinity for sulfhydryl groups, and hence can inhibit enzymes; however, cells treated with cadmium showed proliferation of peroxisomes, which contain catalase, an enzyme. It appears that cadmium at first inhibits catalase activity and then, after a time, enhances that activity. In addition, cadmium inhibits enzymes involved in gluconeogenesis (the generation of glycogen for energy production from noncarbohydrate precursors). It also inhibits oxidative phosphorylation (energy production) and depresses trypsin inhibitor capacity.

Cadmium should be kept stored in a tightly closed container in a cool place. It should be kept stored in a separate locked safety storage cabinet

UN2570 Cadmium compounds, Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required.

Any oxide contaminant is removed by filtering the molten metal, under vacuum, through quartz wool. Its solubility in Hg is 5.2% (18o), and it is soluble in mineral acids. [Wagenknecht & Juza in Handbook of Preparative Inorganic Chemistry (Ed. Brauer) Academic Press Vol II p 1092 1965.]

The space lattice of Cadmium belongs to the hexagonal system, and its closely-packed hexagonal lattice has lattice constants of a=0.2973 nm and c=0.5607 nm.

As indicated in the Exposure and Exposure Monitoring section, cadmium is widely distributed in the environment from a variety of natural and anthropogenic sources. Cadmium emitted into the air is often found bound to small particulates and can travel with these particulates over long distances. As a result, cadmium can remain in the atmosphere for long periods of time until it is deposited by gravitational settling or in rain and snow. Cadmium tends to be more mobile in water than other heavy metals although it will complex with humic substances and can precipitate out under certain conditions. Cadmium can bioaccumulate in aquatic organisms; the degree of accumulation is associated with the pH and humic content of the water. It can also bioaccumulate in plants and in the animals that feed on these plants; for example, cattle and wildlife. However, terrestrial bioaccumulation is much lower than that in water and cadmium concentrations at the top of the terrestrial food chain are not much higher than those at the lower end of the chain.

Air exposure with cadmium powder may cause self-ignition. Moist air slowly oxidizes cadmium forming cadmium oxide. Cadmium dust is incompatible with strong oxidizers, ammonium nitrate; elemental sulfur; hydrazoic acid; selenium, zinc, tellurium. Contact with acids cause a violent reaction, forming flammable hydrogen gas.

The initial risk screening level (IRSL) for cadmium is 0.0006 μg/m3 (annual averaging time) based on the Environmental Protection Agency’s (EPA’s) inhalation unit risk, 0.0018 per μg/m3 (EPA 1992, MDNR 1992).

With cadmium compounds in general, precipitation from solution as sulfides, drying and return of the material to suppliers for recovery is recommended. Cadmium may be recovered from battery scrap as an alternative to disposal. In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers. Must be disposed properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office.

On exposures to cadmium, wash the skin immediately with plenty of water and a nonabrasive soap. Workers should cover the exposed skin with an emollient.