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copper

 
Dictionary: cop·per1   (kŏp'ər) pronunciation
 
n.
  1. (Symbol Cu) A ductile, malleable, reddish-brown metallic element that is an excellent conductor of heat and electricity and is widely used for electrical wiring, water piping, and corrosion-resistant parts, either pure or in alloys such as brass and bronze. Atomic number 29; atomic weight 63.54; melting point 1,083°C; boiling point 2,595°C; specific gravity 8.96; valence 1, 2.
  2. A coin, usually of small denomination, made of copper or a copper alloy.
  3. Chiefly British. A large cooking pot made of copper or often of iron.
  4. Any of various small butterflies of the subfamily Lycaeninae, having predominantly copper-colored wings.
  5. A reddish brown.
tr.v., -pered, -per·ing, -pers.
  1. To coat or finish with a layer of copper.
  2. Slang. To bet against, as in faro.

[Middle English coper, from Old English, from Late Latin cuprum, from Latin Cyprium (aes), Cyprian (metal), from Cyprius, of Cyprus, from Greek Kuprios, from Kupros, Cyprus.]

coppery cop'per·y adj.
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How Products are Made: How is copper made?
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Background

Copper is one of the basic chemical elements. In its nearly pure state, copper is a reddish-orange metal known for its high thermal and electrical conductivity. It is commonly used to produce a wide variety of products, including electrical wire, cooking pots and pans, pipes and tubes, automobile radiators, and many others. Copper is also used as a pigment and preservative for paper, paint, textiles, and wood. It is combined with zinc to produce brass and with tin to produce bronze.

Copper was first used as early as 10,000 years ago. A copper pendant from about 8700 B.C. was found in what is now northern Iraq. There is evidence that by about 6400 B.C. copper was being melted and cast into objects in the area now known as Turkey. By 4500 B.C., this technology was being practiced in Egypt as well. Most of the copper used before 4000 B.C. came from the random discovery of isolated outcroppings of native copper or from meteorites that had impacted Earth. The first mention of the systematic extraction of copper ore comes from about 3800 B.C. when an Egyptian reference describes mining operations on the Sinai Peninsula.

In about 3000 B.C., large deposits of copper ore were found on the island of Cyprus in the Mediterranean Sea. When the Romans conquered Cyprus, they gave the metal the Latin name aes cyprium, which was often shortened to cyprium. Later this was corrupted to cuprum, from which the English word copper and the chemical symbol Cu are derived.

In South America, copper objects were being produced along the northern coast of Peru as early as 500 B.C., and the development of copper metallurgy was well advanced by the time the Inca empire fell to the conquering Spanish soldiers in the 1500s.

In the United States, the first copper mine was opened in Branby, Connecticut, in 1705, followed by one in Lancaster, Pennsylvania, in 1732. Despite this early production, most copper used in the United States was imported from Chile until 1844, when mining of large deposits of high-grade copper ore around Lake Superior began. The development of more efficient processing techniques in the late-1800s allowed the mining of lower-grade copper ores from huge open-pit mines in the western United States.

Today, the United States and Chile are the world's top two copper producing countries, followed by Russia, Canada, and China.

Raw Materials

Pure copper is rarely found in nature, but is usually combined with other chemicals in the form of copper ores. There are about 15 copper ores mined commercially in 40 countries around the world. The most common are known as sulfide ores in which the copper is chemically bonded with sulfur. Others are known as oxide ores, carbonate ores, or mixed ores depending on the chemicals present. Many copper ores also contain significant quantities of gold, silver, nickel, and other valuable metals, as well as large quantities of commercially useless material. Most of the copper ores mined in the United States contain only about 1.2-1.6% copper by weight.

The most common sulfide ore is chalcopyrite, CuFeS2, also known as copper pyrite or yellow copper ore. Chalcocite, Cu2S, is another sulfide ore.

Cuprite, or red copper ore, Cu2O, is an oxide ore. Malachite, or green copper ore, Cu(OH)2•CuCO3, is an important carbonate ore, as is azurite, or blue copper carbonate, Cu(OH)2•2CuCO3.

Other ores include tennantite, boronite, chrysocolla, and atacamite.

In addition to the ores themselves, several other chemicals are often used to process and refine copper. These include sulfuric acid, oxygen, iron, silica, and various organic compounds, depending on the process used.

The Manufacturing
Process

The process of extracting copper from copper ore varies according to the type of ore and the desired purity of the final product. Each process consists of several steps in which unwanted materials are physically or chemically removed, and the concentration of copper is progressively increased. Some of these steps are conducted at the mine site itself, while others may be conducted at separate facilities.

Here are the steps used to process the sulfide ores commonly found in the western United States.

Mining

  • Most sulfide ores are taken from huge open-pit mines by drilling and blasting with explosives. In this type of mining, the material located above the ore, called the overburden, is first removed to expose the buried ore deposit. This produces an open pit that may grow to be a mile or more across. A road to allow access for equipment spirals down the interior slopes of the pit.
  • The exposed ore is scooped up by large power shovels capable of loading 500-900 cubic feet (15-25 cubic meters) in a single bite. The ore is loaded into giant dump trucks, called haul trucks, and is transported up and out of the pit.

Concentrating

The copper ore usually contains a large amount of dirt, clay, and a variety of non-copper bearing minerals. The first step is to remove some of this waste material. This process is called concentrating and is usually done by the flotation method.

  • The ore is crushed in a series of cone crushers. A cone crusher consists of an interior grinding cone that rotates on an eccentric vertical axis inside a fixed outer cone. As the ore is fed into the top of the crusher, it is squeezed between the two cones and broken into smaller pieces.
  • The crushed ore is then ground even smaller by a series of mills. First, it is mixed with water and placed in a rod mill, which consists of a large cylindrical container filled with numerous short lengths of steel rod. As the cylinder rotates on its horizontal axis, the steel rods tumble and break up the ore into pieces about 0.13 in (3 mm) in diameter. The mixture of ore and water is further broken up in two ball mills, which are like a rod mill except steel balls are used instead of rods. The slurry of finely ground ore that emerges from the final ball mill contains particles about 0.01 in (0.25 mm) in diameter.
  • The slurry is mixed with various chemical reagents, which coat the copper particles. A liquid, called a frother, is also added. Pine oil or long-chain alcohol are often used as frothers. This mixture is pumped into rectangular tanks, called flotation cells, where air is injected into the slurry through the bottom of the tanks. The chemical reagents make the copper particles cling to the bubbles as they rise to the surface. The frother forms a thick layer of bubbles, which overflows the tanks and is collected in troughs. The bubbles are allowed to condense and the water is drained off. The resulting mixture, called a copper concentrate, contains about 25-35% copper along with various sulfides of copper and iron, plus smaller concentrations of gold, silver, and other materials. The remaining materials in the tank are called the gangue or tailings. They are pumped into settling ponds and allowed to dry.

Smelting

Once the waste materials have been physically removed from the ore, the remaining copper concentrate must undergo several chemical reactions to remove the iron and sulfur. This process is called smelting and traditionally involves two furnaces as described below. Some modern plants utilize a single furnace, which combines both operations.

  • The copper concentrate is fed into a furnace along with a silica material, called a flux. Most copper smelters utilize oxygen-enriched flash furnaces in which preheated, oxygen-enriched air is forced into the furnace to combust with fuel oil. The copper concentrate and flux melt, and collect in the bottom of the furnace. Much of the iron in the concentrate chemically combines with the flux to form a slag, which is skimmed off the surface of the molten material. Much of the sulfur in the concentrate combines with the oxygen to form sulfur dioxide, which is exhausted from the furnace as a gas and is further treated in an acid plant to produce sulfuric acid. The remaining molten material in the bottom of the furnace is called the matte. It is a mixture of copper sulfides and iron sulfides and contains about 60% copper by weight.
  • The molten matte is drawn from the furnace and poured into a second furnace called a converter. Additional silica flux is added and oxygen is blown through the molten material. The chemical reactions in the converter are similar to those in the flash furnace. The silica flux reacts with the remaining iron to form a slag, and the oxygen reacts with the remaining sulfur to form sulfur dioxide. The slag may be fed back into the flash furnace to act as a flux, and the sulfur dioxide is processed through the acid plant. After the slag is removed, a final injection of oxygen removes all but a trace of sulfur. The resulting molten material is called the blister and contains about 99% copper by weight.

Refining

Even though copper blister is 99% pure copper, it still contains high enough levels of sulfur, oxygen, and other impurities to hamper further refining. To remove or adjust the levels of these materials, the blister copper is first fire refined before it is sent to the final electrorefining process.

  • The blister copper is heated in a refining furnace, which is similar to a converter described above. Air is blown into the molten blister to oxidize some impurities. A sodium carbonate flux may be added to remove traces of arsenic and antimony. A sample of the molten material is drawn and an experienced operator determines when the impurities have reached an acceptable level. The molten copper, which is about 99.5% pure, is then poured into molds to form large electrical anodes, which act as the positive terminals for the electrorefining process.
  • Each copper anode is placed in an individual tank, or cell, made of polymer-concrete. There may be as many as 1,250 tanks in operation at one time. A sheet of copper is placed on the opposite end of the tank to act as the cathode, or negative terminal. The tanks are filled with an acidic copper sulfate solution, which acts as an electrical conductor between the anode and cathode. When an electrical current is passed through each tank, the copper is stripped off the anode and is deposited on the cathode. Most of the remaining impurities fall out of the copper sulfate solution and form a slime at the bottom of the tank. After about 9-15 days, the current is turned off and the cathodes are removed. The cathodes now weigh about 300 lb (136 kg) and are 99.95-99.99% pure copper.
  • The slime that collects at the bottom of the tank contains gold, silver, selenium, and tellurium. It is collected and processed to recover these precious metals.

Casting

  • After refining, the copper cathodes are melted and cast into ingots, cakes, billets, or rods depending on the final application. Ingots are rectangular or trapezoidal bricks, which are remelted along with other metals to make brass and bronze products. Cakes are rectangular slabs about 8 in (20 cm) thick and up to 28 ft (8.5 m) long. They are rolled to make copper plate, strip, sheet, and foil products. Billets are cylindrical logs about 8 in (20 cm) in diameter and several feet (meters) long. They are extruded or drawn to make copper tubing and pipe. Rods have a round cross-section about 0.5 in (1.3 cm) in diameter. They are usually cast into very long lengths, which are coiled. This coiled material is then drawn down further to make copper wire.

Quality Control

Because electrical applications require a very low level of impurities, copper is one of the few common metals that are refined to almost 100% purity. The process described above has been proven to produce copper of very high purity. To ensure this purity, samples are analyzed at various steps to determine whether any adjustment to the process is required.

Byproducts/Waste

The recovery of sulfuric acid from the copper smelting process not only provides a profitable byproduct, but also significantly reduces the air pollution caused by the furnace exhaust. Gold, silver, and other precious metals are also important byproducts.

Waste products include the overburden from the mining operation, the tailings from the concentrating operation, and the slag from the smelting operation. This waste may contain significant concentrations of arsenic, lead, and other chemicals, which pose a potential health hazard to the surrounding area. In the United States, the Environmental Protection Agency (EPA) regulates the storage of such wastes and the remediation of the area once mining and processing operations have ceased. The sheer volume of the material involved—in some cases, billions of tons of waste—makes this a formidable task, but it also presents some potentially profitable opportunities to recover the useable materials contained in this waste.

The Future

Demand for copper is expected to remain high, especially in the electrical and electronics industries. The current trends in copper processing are towards methods and equipment that use less energy and produce less air pollution and solid waste. In the United States, this is a difficult assignment because of the stringent environmental controls and the very low-concentration copper ores that are available. In some cases, the production costs may increase significantly.

One encouraging trend is the increased use of recycled copper. Currently over half the copper being produced in the United States comes from recycled copper. Fifty-five percent of the recycled copper comes from copper machining operations, such as screw forming, and 45% comes from the recovery of used copper products, such as electrical wire and automobile radiators. The percentage of recycled copper is expected to grow as the costs of new copper processing increase.

Where to Learn More

Books

Brady, George S., Henry R. Clauser, and John A. Vaccari. Materials Handbook. McGraw-Hill, 1997.

Heiserman, David L. Exploring Chemical Elements and Their Compounds. TAB Books, 1992.

Hombostel, Caleb. Construction Materials. John Wiley and Sons, Inc., 1991.

Kroschwitz, Jacqueline I. and Mary Howe-Grant, ed. Encyclopedia of Chemical Technology. John Wiley and Sons, Inc., 1993.

Stwertka, Albert. A Guide to the Elements. Oxford University Press, 1996.

Periodicals

Baum, Dan and Margaret L. Knox. "We want people who have a problem with mine wastes to think of Butte." Smithsonian (November 1992): 46-52, 54-57.

Shimada, Izumi and John F. Merkel. "Copper-Alloy Metallurgy in Ancient Peru." Scientific American (July 1991): 80-86.

Other

http://www.copper.org.

http://www.intercorr.com/periodic/29.htm.

http://innovations.copper.org/innovations.html.

[Article by: Chris Cavette]


 

A chemical element, Cu, atomic number 29, atomic weight 63.546. Copper, a nonferrous metal, is the twentieth most abundant element present in the Earth's crust, at an average level of 68 parts per million (0.22 lb/ton or 0.11 kg/metric ton). Copper metal and copper alloys have considerable technological importance due to their combined electrical, mechanical, and physical properties. The discoveries that mixed-valence Cu(II)/Cu(III) oxides exhibit superconductivity (zero electrical resistance) at temperatures as high as 125 K (−234°F; liquid nitrogen, a cheap coolant, boils at 90 K or −297°F) have generated intense international competition to understand these new materials and to develop technological applications. Although some pure copper metal is present in nature, commercial copper is obtained by reduction of the copper compounds in ores followed by electrolytic refining. The rich chemistry of copper is restricted mostly to the valence states Cu(I) and Cu(II); compounds containing Cu(0), Cu(III), and Cu(IV) are uncommon. Soluble copper salts are potent bacteriocides and algicides at low levels and toxic to humans in large doses. Yet copper is an essential trace element that is present in various metalloproteins required for the survival of plants and animals.

Copper is located in the periodic table between nickel and zinc in the first row of transition elements and in the same subgroup as the other so-called coinage metals, silver and gold. The electronic configuration of elemental copper is [1s22s22p63s2] 3d104s1 or [argon]3d104s1. At first glance, the sole 4s electron might suggest chemical similarity to potassium, which has the [argon]4s1 configuration. However, metallic copper, in sharp contrast to metallic potassium, is relatively unreactive. The higher nuclear charge of copper relative to that of potassium is not fully shielded by the 10 additional d electrons, with the result that the copper 4s electron has a higher ionization potential than that of potassium (745.5 versus 418.9 kilojoules/mole, respectively). Moreover, the second and third ionization potentials of copper (1958.1 and 3554 J/mole, respectively) are considerably lower than those of potassium, and account for the higher valence-state accessibility associated with transition-metal chemistry as opposed to alkali-metal chemistry. See also Electron configuration; Periodic table; Transition elements; Valence.

Copper is a comparatively heavy metal. The density of the pure solid is 8.96 g/cm3 (5.18 oz/in.3) at 20°C (68°F). The density of commercial copper varies with method of manufacture, averaging 8.90–8.92 g/cm3 (5.14–5.16 oz/in.3) in cast refinery shapes, 8.93 g/cm3 (5.16 oz/in.3) for annealed tough-pitch copper, and 8.94 g/cm3 (517 oz/in.3) for oxygen-free copper. The density of liquid copper is 8.22 g/cm3 (4.75 oz/in.3) near the freezing point.

The melting point of copper is 1083.0 ∓ 0.1°C (1981.4 ∓ 0.2°F). Its normal boiling point is 2595°C (4703°F).

The coefficient of linear expansion of copper is 1.65 × 10−5/°C at 20°C.

The specific heat of the solid is 0.092 cal/g at 20°C (68°F). The specific heat of liquid copper is 0.112 cal/g, and of copper in the vapor state about 0.08 cal/g.

The electrical resistivity of copper in the usual volumetric unit, that of a cube measuring 1 cm in each direction, is 1.6730 × 10−6 ohm · cm at 20°C (68°F). Only silver has a greater volumetric conductivity than copper. On a relative basis in which silver is rated 100, copper is 94, aluminum 57, and iron 16.

The mass resistivity of pure copper for a length of 1 m weighing 1 g at 20°C (68°F) is 0.14983 ohm. The conductivity of copper on the mass basis is surpassed by several light metals, notably aluminum. The relative values are 100 for aluminum, 50 for copper, and 44 for silver.

By far the largest use of copper is in the electrical industry, and therefore high electrical conductivity is its most important single property, although for industrial use this property must be accompanied by suitable characteristics in other respects. See also Conductor (electricity).

Copper-containing proteins provide diverse biochemical functions, including copper uptake and transport (ceruloplasmin), copper storage (metallothionen), protective roles (superoxide dismutase), catalysis of substrate oxygenation (dopamine β-monooxygenase), biosynthesis of connective tissue (lysyl oxidase), terminal oxidases for oxygen metabolism (cytochrome c oxidase), oxygen transport (hemocyanin), and electron transfer in photosynthetic pathways (plastocyanin). See also Enzyme.


 
Food and Nutrition: copper
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A dietary essential trace metal, which forms the prosthetic group of a number of enzymes. The Reference Nutrient Intake is 1.2 mg/day. Toxic in excess, and it is recommended that not more than 2-10 mg/day should be consumed habitually. Rich sources include: meat, poultry, game, fish and shellfish, avocado, nuts, pulses, bread, chocolate, beer, cider, coconut, mushrooms.

 
Food and Fitness: copper
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An essential element involved in many processes including red blood cell formation, respiration, and bone formation. Copper deficiencies are rare, mainly because most domestic water supplies are contaminated with copper from pipes, but low intakes can lead to anaemia. Oysters and liver are good sources of dietary copper. In the UK, the adult Reference Nutrient Intake for copper is 1.2 mg each day. In the USA, the estimated safe and adequate daily intake of copper is 1.5-3.0 mg. Blood levels of copper often decrease after exercise indicating that athletes may need higher than normal intakes. Copper and zinc appear to be antagonistic; high intakes of one tend to reduce the absorption of the other. Copper toxicity is rare, but intakes greater than 20 mg cause vomiting and nausea.

 
Hacker Slang: copper
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Conventional electron-carrying network cable with a core conductor of copper — or aluminum! Opposed to light pipe or, say, a short-range microwave link.


 

Description

Copper is an essential mineral that plays an important role in iron absorption and transport. It is considered a trace mineral because it is needed in very small amounts. Only 70–80 mg of copper are found in the body of a normal healthy person. Even though the body needs very little, copper is an important nutrient that holds many vital functions in the body.

Copper is essential for normal development of the body because it:

  • Participates in a wide variety of important enzymatic reactions in the body.
  • Is a component of or a cofactor for approximately 50 different enzymes. These enzymes need copper to function properly.
  • Is essential for iron absorption and transport. Iron is needed to make hemoglobin, a main component of red blood cells. Therefore, copper deficiency is often linked to iron-deficiency anemia.
  • Is required to build elastin and collagen, which are an important components of bones and connective tissues. Therefore, copper is believed to protect the bones and joints against degeneration and osteoporosis.
  • Is required for melanin production. People with copper deficiency may have pale skin and hair.
  • Is a key mineral for the immune system. Copper promotes wound healing. Studies show that premature infants or children with genetic copper defects are at high risk of getting infections and would significantly improve with copper supplementation.
  • Attacks free radicals. Copper is a strong antioxidant. It works by attaching itself to the enzyme Superoxide dismutase (SOD). Copper also binds to a protein to form ceruloplasmin, which is an antioxidant.
  • Helps the body produce energy. Copper participates in many oxidative reactions that break down fats in fat tissue to produce much needed energy. Copper deficiency has been associated with high cholesterol levels.
  • Is necessary for normal functioning of insulin. Copper deficiency is also associated with poor blood glucose control.
  • Is needed for normal functioning of the cardiovascular system.
  • Protects the structure and function of the nervous system, including the brain. Copper protects nerve fiber by maintaining myelin, the insulating sheath that surrounds nerve cells. It also aids the transmission of nerve signals in the brains.

General Use

Copper supplements may be beneficial in treating or preventing copper deficiency. Copper deficiency used to be relatively rare because the body requires so little of it, only about 2 mg per day. In addition, it is available naturally in a variety of foods such as whole grains, shellfish, nuts, beans, and leafy vegetables. Additional sources of copper are the copper water pipes that run through homes or the copper cookware in the kitchen. These sources leach copper into the water we drink and the food we eat. The level of copper in drinking water is sometimes so high that it becomes a public concern. However, scientists now realize that copper deficiency, especially borderline cases, is more common than once thought. Copper deficiency is currently on the rise due to a decrease of whole foods in the diet and high consumption of fatty and processed foods.

It was discovered in 2001 that vegetarian diets generally contain more copper, but that the absorption efficiency was lower for lactoovo vegetarians than for nonvegetarians. The study also showed that the increased amounts of copper in the vegetarian diets allow for greater copper content.

Besides dietary causes, certain diseases or conditions may reduce copper absorption, transport or increase its requirements, resulting in abnormally low copper blood levels. Increased copper intake through diet or supplementation may be necessary in the following conditions:

  • premature infants fed only cow's milk
  • pregnant women
  • malnutrition
  • celiac disease, sprue, cystic fibrosis, or short-bowel syndrome (these diseases cause poor absorption of dietary copper)
  • kidney disease
  • high consumption of zinc or iron (these minerals interfere with copper absorption)
  • highly processed foods (copper is stripped away during food processing)
  • Menkes syndrome (copper deficiency is caused by genetic defects of copper transport; Menkes syndrome patients cannot use copper supplied by the diet efficiently)

Symptoms of copper deficiency include:

  • anemia
  • malnourished infants
  • prominently dilated veins
  • pale hair or skin
  • poorly formed bones
  • nervous system disorders
  • high cholesterol levels
  • heart disease
  • loss of taste
  • increased susceptibility to infections
  • infertility
  • birth defects

Exceeding the daily requirement is dangerous, however, because copper toxicity commonly occurs. Copper toxicity is a very serious medical problem. Acute toxicity due to ingestion of too much supplement, for example, may cause nausea, vomiting, abdominal pain, diarrhea, dizziness, headache, and a metallic taste in the mouth. Chronic toxicity is often caused by genetic defects of copper metabolism, such as Wilson's disease. In this disease, copper is not eliminated properly and is allowed to accumulate to toxic levels. Copper is therefore present at high concentration where it should not be, such as in the liver, the lens of the eye, kidneys, or brain.

Disease Prevention

Copper is a good antioxidant. It works together with an antioxidant enzyme, superoxide dismutase (SOD), to protect cell membranes from being destroyed by free radicals. Free radicals are any molecules that are missing one electron. Because this is an unbalanced and unstable state, a radical is desperately finding ways to complete its pair. Therefore, it reacts to any nearby molecules to either steal an electron or give away the unpaired one. In the process, free radicals initiate chain reactions that destroy cell structures. Like other antioxidants, copper scavenges or cleans up these highly reactive radicals and changes them into inactive, less harmful compounds. Therefore, it can help prevent cancer. In 2001, a study reported that concentrations of copper sulfate and ascorbate may inhibit breast cancer growth. With further study, the combination may even prove useful as a chemotherapy agent for certain breast cancer patients.

Copper may also help prevent degenerative diseases or conditions such as premature aging, heart disease, autoimmune diseases, arthritis, cataracts, Alzheimer's disease, or diabetes.

Osteoporosis

Copper may play a role in preventing osteoporosis. Calcium and vitamin D have long been considered the mainstay of osteoporosis treatment and prevention. However, a recent study has shown that they can be even more effective in increasing bone density and preventing osteoporosis if they are used in combination with copper and two other trace minerals, zinc and manganese.

Rheumatoid Arthritis

Copper has been a folklore remedy for rheumatoid arthritis since 1500 B.C. in ancient Egypt. Some people believe that wearing jewelry made of copper may relieve arthritic symptoms. To evaluate the effect of copper for the treatment of rheumatoid arthritis, Dr. Walker and his colleagues conducted a study of 77 arthritic patients. Patients were divided into two groups: treatment group wearing copper jewelry and placebo group wearing nothing or aluminum jewelry. In this study, patients who wore copper bracelets felt significantly better than those in the placebo group. In addition, patients in the treatment group reported recurrences of symptoms after the bracelets were removed. To explain the effects of the copper bracelets, these researchers suggested that copper contained in the bracelets was dissolved in sweat and then absorbed through the skin. They suspected that copper's effectiveness may be related to its role as an antioxidant. They also believe that copper may function as both an anti-inflammatory agent and as an antioxidant. Thus, it is possibly effective in reducing inflammatory response to such conditions as rheumatoid arthritis.

Preparations

Copper is contained in many multivitamin/mineral preparations. It is also available as a single ingredient in the form of tablets. These tablets should be swallowed whole with a cup of water, preferably with meals, to avoid stomach upset. A person may choose any of the following preparations: copper gluconate, copper sulfate, or copper citrate. However, copper gluconate may be the least irritating to the stomach.

Zinc and copper compete with each other for absorption in the gastrointestinal tract. As a result, excessive copper intake may cause zinc deficiency, and vice versa. Therefore, a person should take zinc and copper supplements together in ratios of 10:1 or 15:1.

Precautions

Those adding copper supplements to their diets should consider:

  • Informing their doctors for proper instruction and monitoring of side effects. Copper toxicity due to excessive doses of copper supplements has been reported.
  • Although there currently is no recommended daily allowance (RDA) established for copper, 2 mg of copper per day is considered sufficient and safe. Nausea and vomiting may occur in persons taking more than 20 mg of copper daily.
  • It is not known if copper supplementation may harm a growing fetus. However, as with any drugs, pregnant or nursing women should not take copper or any other supplements or drugs without first consulting their doctors.
  • In certain areas, drinking water may contain high levels of copper. Periodic checks of copper levels in drinking water may be necessary.
  • Because individual antioxidants often work together as a team to defend the body against free radicals, the balance between copper, zinc, and iron must be maintained. Excessive intake of one nutrient might result in a deficiency of other minerals and decreased resistance to infections and increased risk of heart disease, diabetes, arthritis, and other diseases.

Side Effects

A person should stop taking copper supplements and seek medical help immediately if having the following signs or symptoms:

  • anemia
  • nausea
  • vomiting
  • abdominal pain

Interactions

Factors That Increase Copper Concentrations

Certain disorders have been known to increase copper levels. Persons with these conditions should not take copper supplements as they may cause copper toxicity.

  • recent heart attacks
  • lupus erythematosus
  • cirrhosis of the liver
  • schizophrenia
  • leukemia and some other forms of cancer
  • viral infections
  • ulcerative colitis (This inflammatory bowel disease may cause accumulation of copper in the body. Excessive amount of copper may worsen many symptoms of this disease by increasing susceptibility to infections and inhibiting wound healing.)
  • Wilson's disease (This disease causes accumulation of copper in the tissues. As a result, patients have liver disease, mental retardation, tremor and poor muscle coordination. They also have copper deposits in the cornea of the eye. To manage this disease, patients are put on a low-copper diet and given penicillamine, a drug that attaches itself to copper and increases its excretion.)

Resources

Books

Lieberman,, Shari and Nancy Bruning. "Copper." In The Real Vitamin & Mineral Book: Using Supplements for Optimum Health Garden City Park, NY: Avery Publishing Group, 1997.

Passwater, Richard A. All About Antioxidants. Garden City Park, NY: Avery Publishing Group, 1998.

Periodicals

Gonzalez, M. J, et al. "Inhibition of Human Breast Carcinoma Cell Proliferation by Ascorbate and Copper."The Journal of Nutrition 131, no. 11 (November 2001): 3142S.

Hunt, Janet R., and Richard A. Vanderpool. "Apparent Copper Absorption from a Vegetarian Diet."American Journal of Clinical Nutrition 74, no. 6 (December 2001): 803–805.

Reginster, Jean-Yves, Anne Noel Taquet, and Christiane Gosset. "Therapy for Osteoporosis: Miscellaneous and Experimental Agents."Endocrinology and Metabolism Clinics (June 1998): 453–463.

Uauy, Ricardo, Manuel Olivarez, and Mauricio Gonzales. "Essentiality of Copper in Humans."American Journal of Clinical Nutrition 67 suppl (1998): 952S–959S.

Other

"Copper" The Merck Manual of Diagnosis and Therapy. [cited October 2002]. . Rosenstein, Elliot D., and Jacques R. Caldwell. "Therapies: Trace Elements in the Treatment of Rheumatic Conditions." In Rheumatic Diseases Clinics of North America. Part II. [cited May 2000]. .

[Article by: Mai Tran; Teresa G. Odle]

 

Crystalline copper from Michigan
(click to enlarge)
Crystalline copper from Michigan (credit: Courtesy of Ted Boente Collection; photograph, John H. Gerard)
Metallic chemical element, one of the transition elements, chemical symbol Cu, atomic number 29. Sometimes found in the free state in nature, it is a reddish metal, very ductile and an unusually good conductor of electricity and heat. Most of the world's copper production is used by the electrical industries; the remainder is combined with other metals (e.g., zinc, tin, nickel) to form alloys such as brass, bronze, nickel silver, and Monel. Copper is part of nearly all coinage metals. In compounds copper usually has valence 1 (cuprous) or 2 (cupric). Cuprous compounds include cuprous oxide, a red pigment and a fungicide; cuprous chloride, a catalyst for certain organic reactions; and cuprous sulfide, with a variety of uses. Cupric compounds include cupric oxide, a pigment, decolorizing agent, and catalyst; cupric chloride, a catalyst, wood preservative, mordant, disinfectant, feed additive, and pigment; and cupric sulfate, a pesticide, germicide, feed additive, and soil additive. Copper is a necessary trace element in the human diet and essential to plant growth; in blue-blooded mollusks and crustaceans it plays the same role in hemocyanin as iron does in hemoglobin.

For more information on copper, visit Britannica.com.

 
Architecture: copper
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A lustrous reddish metal, highly ductile and malleable; has high tensile strength, is an excellent electrical and thermal conductor, is available in a wide variety of shapes; widely used for downspouts, electrical conductors, flashing, gutters, roofing, etc.


 

[Ma]

One of the first metals (Cu) to be exploited by human communities. In its native form it can be worked without prior treatment. It was later extracted from a range of ores: carbonates (including malachite and azurite); oxides (including cuprite and melaconite); and sulphides (including chalcanthite). Shaping could be done by hammering, casting, or a combination of the two. Copper provides the main constituent for a number of alloys, the most widely used being bronze. The development of copper metallurgy happened independently in several parts of the world: in western Asia around 6000 bc; in Europe around 4000 bc; in the Longshan Culture of China around 2500 bc; in South America around 1500 bc in Peru, Bolivia, and Ecuador; ad 100 in central America; and in North America amongst the Old Copper Cultures of the Great Lakes region around 3000 bc.

 

An essential element involved in many processes including red blood cell formation, blood-sugar regulation, and bone formation. Deficiency may cause anaemia and feelings of lassitude.

 
copper, metallic chemical element; symbol Cu [Lat. cuprum=copper]; at. no. 29; at. wt. 63.546; m.p. 1,083.4°C; b.p. 2,567°C; sp. gr. 8.96 at 20°C; valence +1 or +2. Copper and some of its alloys have been used by humanity since the Bronze Age. One of the first metals known to humans, free copper was probably mined in the Tigris-Euphrates valley as long ago as the 5th cent. B.C. Cyprus, from which the metal's name originally comes, was the primary source of copper in the ancient world.

Properties

Copper is a reddish metal with a face-centered cubic crystalline structure. It is malleable, ductile, and an extremely good conductor of both heat and electricity. It is softer than iron but harder than zinc and can be polished to a bright finish. It is found in Group 11 of the periodic table, together with silver and gold. Copper has low chemical reactivity. In moist air it slowly forms a greenish surface film (usually a mixture of carbonate, sulfate, hydroxide, and oxide) called patina; this coating protects the metal from further attack. Copper dissolves in hot concentrated hydrochloric or sulfuric acid but is little affected by cold solutions of these acids; it also dissolves in nitric acid. Salt water corrodes copper, forming a chloride.

Compounds

The most important chemical compound of copper is copper sulfate pentahydrate, also called bluestone or blue vitriol. Other compounds include Paris green, Bordeaux mixture, a cyanide, a chloride, oxides, and a basic carbonate. Verdigris is basic copper acetate.

Sources and Ores

Small amounts of copper are found uncombined, particularly near Lake Superior in Michigan. Copper ores are found in various parts of the world. In the United States (the chief producer of copper) ores are mined in Arizona, Utah, Montana, New Mexico, Nevada, and Michigan. Copper ores are also found in Canada, South America (in Chile and Peru), S central Africa, Russia (in the Ural Mts.), and to a limited extent in Europe and the British Isles.

The principal ore of copper is chalcopyrite, a sulfide of copper and iron, also called copper pyrite. Other important ores are chalcocite, or copper glance, a shiny lead-gray copper sulfide; bornite, a lustrous reddish-brown sulfide of copper and iron; cuprite, a red cuprous oxide ore; and malachite, a bright green carbonate ore. Azurite is a blue crystalline basic carbonate of copper found with other copper ores. Chrysocolla is a bluish-green copper silicate ore. Another important source of copper is secondary (scrap) copper, which is produced from discarded copper and copper alloys.

Commercial Preparation

Copper metal is prepared commercially in various ways. Copper sulfide ores, usually containing only 1% to 2% copper, are concentrated to 20% to 40% copper by the flotation process. They are then usually roasted to remove some of the sulfur and other impurities, and then smelted with iron oxide in either a blast furnace or a reverberatory furnace to produce copper matte, a molten solution of copper sulfide mixed with small amounts of iron sulfide. The matte is transferred to a converter, where it is treated by blowing air through it to remove the sulfur (as sulfur dioxide, a gas) and the iron (as a slag of ferrous oxide). The resulting copper is 98% to 99% pure; it is called blister copper because its surface is blistered by escaping gases when it solidifies during casting.

Most copper is further purified by electrolysis. The blister copper is refined in a furnace and cast into anodes. Thin sheets of pure copper are used as cathodes. A solution of copper sulfate and sulfuric acid is used as the electrolyte. When the anode and cathode are immersed in the electrolyte and an electric current is passed, the anode is dissolved in the electrolyte and pure copper metal is deposited on the cathode. Soluble impurities, usually nickel and arsenic, remain dissolved in the electrolyte. Insoluble impurities, often including silver, gold, and other valuable metals, settle out of the electrolyte; they may be collected and purified.

Copper oxide ores are usually treated by a different process, called leaching, in which the copper in the ore is dissolved in a leaching solution (usually dilute sulfuric acid); pure copper is recovered by electrolysis. Alternatively, the solution is treated with iron to precipitate the so-called cement copper, which is impure.

Importance and Uses

Copper is present in minute amounts in the animal body and is essential to normal metabolism. It is a component of hemocyanin, the blue, oxygen-carrying blood pigment of lobsters and other large crustaceans. It is needed in the synthesis of hemoglobin, the red, oxygen-carrying pigment found in the blood of humans, although it is not a component of hemoglobin.

The chief commercial use of copper is based on its electrical conductivity (second only to that of silver); about half the total annual output of copper is employed in the manufacture of electrical apparatus and wire. Copper is also used extensively as roofing, in making copper utensils, and for coins and metalwork. Copper tubing is used in plumbing, and, because of its high heat conductivity, in heat-exchanging devices such as refrigerator and air-conditioner coils. Powdered copper is sometimes used as a pigment in paints. An important use of copper is in alloys such as brass, bronze, gunmetal, Monel metal, and German silver. Compounds of copper are widely used as insecticides and fungicides; as pigments in paints; as mordants (fixatives) in dyeing; and in electroplating.


 

Cu
Cubic -- hexoctahedral

Environment

In the upper levels of copper sulfide veins and in some types of volcanic rock.

Crystal description

Usually in distorted, often rounded, complex crystals, with cubes, dodecahedrons, and octahedrons predominant. Often in hackly masses (Michigan) and in sheets without recognizable crystal forms.

Physical properties

Copper color. Luster metallic; hardness 2Ɖ-3; specific gravity 8.9. Malleable and ductile.

Composition

Fairly pure as a rule, often alloyed with small amounts of silver, arsenic, iron, etc.

Tests

Small bits fuse on charcoal to black-coated copper button; malleable, soluble in acids, giving greenish solutions. Colors flame blue-green.

Distinguishing characteristics

Almost inescapable green and blue stains on rock outcrops, known as "copper blooms," are a guide to deposits of copper and its associated minerals. The malleability and the color are distinguishing characteristics.

Occurrence

Since weathering processes free copper from its primary ore, chalcopyrite (CuFeS 2 ), it is likely to be found in the cap rock (the gossan) of copper-bearing sulfide veins, particularly in arid climates. Native copper is also found in ancient lava flows, where iron and oxygen have robbed the magma of sulfur. It is abundant in this form in Michigan's Upper Peninsula, where copper has been deposited in a thick series of flows, and this is the only economic source where all the copper is in the native state. Great masses found in these deposits were hard to remove because of their size and the difficulty of breaking them up. Nuggets from this deposit carried south by the glacier were scattered across the north-central states and were manufactured by the Indians into copper artifacts. Native copper was once found in Chessy, France, and Cornwall, England. Today it is abundant in some of the Arizona mines still working in the upper levels, like Morenci and Ajo. Surprisingly, it is not a major mineral in Chile, though that country contains rich sources of the metal.



 
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pronunciation

IN BRIEF: A reddish metal.

pronunciation They discovered the plumbing was made of copper pipes.

 
Wikipedia: Copper
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29 nickelcopperzinc
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Cu

Ag
Copper in the periodic table of the elements
General
Name, symbol, number copper, Cu, 29
Element category transition metal
Group, period, block 114, d
Appearance metallic copper
Standard atomic weight 63.546(3)g·mol−1
Electron configuration [Ar] 3d10 4s1
Electrons per shell 2, 8, 18, 1 (Image)
Physical properties
Phase solid
Density (near r.t.) 8.94 g·cm−3
Liquid density at m.p. 8.02 g·cm−3
Melting point 1357.77 K
(1084.62 °C, 1984.32 °F)
Boiling point 2835 K
(2562 °C, 4643 °F)
Heat of fusion 13.26 kJ·mol−1
Heat of vaporization 300.4 kJ·mol−1
Specific heat capacity (25 °C) 24.440 J·mol−1·K−1
Vapor pressure
P/Pa 1 10 100 1 k 10 k 100 k
at T/K 1509 1661 1850 2089 2404 2834
Atomic properties
Crystal structure face centered cubic
0.3610 nm
Oxidation states +1, +2, +3, +4
(mildly basic oxide)
Electronegativity 1.90 (Pauling scale)
Ionization energies
(more)
1st: 745.5 kJ·mol−1
2nd: 1957.9 kJ·mol−1
3rd: 3555 kJ·mol−1
Atomic radius 128 pm
Covalent radius 132±4 pm
Van der Waals radius 140 pm
Miscellaneous
Magnetic ordering diamagnetic
Electrical resistivity (20 °C) 16.78 nΩ·m
Thermal conductivity (300 K) 401 W·m−1·K−1
Thermal expansion (25 °C) 16.5 µm·m−1·K−1
Speed of sound (thin rod) (r.t.) (annealed)
3810 m·s−1
Young's modulus 110–128 GPa
Shear modulus 48 GPa
Bulk modulus 140 GPa
Poisson ratio 0.34
Mohs hardness 3.0
Vickers hardness 369 MPa
Brinell hardness 874 MPa
CAS registry number 7440-50-8
Most stable isotopes
Main article: Isotopes of copper
iso NA half-life DM DE (MeV) DP
63Cu 69.15% 63Cu is stable with 34 neutrons
65Cu 30.85% 65Cu is stable with 36 neutrons
References
copper disc made by continuous casting, etched

Copper (pronounced /ˈkɒpər/) is a chemical element with the symbol Cu (Latin: cuprum) and atomic number 29. It is a ductile metal with very high thermal and electrical conductivity. Pure copper is rather soft and malleable and a freshly-exposed surface has a pinkish or peachy color. It is used as a thermal conductor, an electrical conductor, a building material, and a constituent of various metal alloys.

Copper metal and alloys have been used for thousands of years. In the Roman era, copper was principally mined on Cyprus, hence the origin of the name of the metal as Cyprium, "metal of Cyprus", later shortened to Cuprum. There may be insufficient reserves to sustain current high rates of copper consumption.[1] Some countries, such as Chile and the United States, still have sizable reserves of the metal which are extracted through large open pit mines.

Copper compounds are known in several oxidation states, usually 2+, where they often impart blue or green colors to natural minerals such as turquoise and have been used historically widely as pigments. Copper as both metal and pigmented salt, has a significant presence in decorative art. Copper 2+ ions are soluble in water, where they function at low concentration as bacteriostatic substances and fungicides. For this reason, copper metal can be used as an anti-germ surface that can add to the anti-bacterial and antimicrobial features of buildings such as hospitals.[2] In sufficient amounts, copper salts can be poisonous to higher organisms as well. However, despite universal toxicity at high concentrations, the 2+ copper ion at lower concentrations is an essential trace nutrient to all higher plant and animal life. In animals, including humans, it is found widely in tissues, with concentration in liver, muscle, and bone. It functions as a co-factor in various enzymes and in copper-based pigments.

Contents

History

Copper Age

Copper, as native copper, is one of the few metals to occur naturally as an un-compounded mineral. Copper was known to some of the oldest civilizations on record, and has a history of use that is at least 10,000 years old. Some estimates of copper's discovery place this event around 9000 BC in the Middle East.[3] A copper pendant was found in what is now northern Iraq that dates to 8700 BC.[4] It is probable that gold and meteoritic iron were the only metals used by humans before copper.[5] By 5000 BC, there are signs of copper smelting: the refining of copper from simple copper compounds such as malachite or azurite. Among archaeological sites in Anatolia, Çatal Höyük (~6000 BC) features native copper artifacts and smelted lead beads, but no smelted copper. Can Hasan (~5000 BC) had access to smelted copper but the oldest smelted copper artifact found (a copper chisel from the chalcolithic site of Prokuplje in Serbia) has pre-dated Can Hasan by 500 years. The smelting facilities in the Balkans appear to be more advanced than the Turkish forges found at a later date, so it is quite probable that copper smelting originated in the Balkans. Investment casting was realized in 4500-4000 BCE in Southeast Asia.[3]

Ancient Copper ingot from Zakros, Crete is shaped in the form of an animal skin typical for that era.

Copper smelting appears to have been developed independently in several parts of the world. In addition to its development in the Balkans by 5500 BC, it was developed in China before 2800 BC, in the Andes around 2000 BC, in Central America around 600 AD, and in West Africa around 900 AD.[6] Copper is found extensively in the Indus Valley Civilization by the 3rd millennium BC. In Europe, Ötzi the Iceman, a well-preserved male dated to 3300-3200 BC, was found with an axe with a copper head 99.7% pure. High levels of arsenic in his hair suggest he was involved in copper smelting. Over the course of centuries, experience with copper has assisted the development of other metals; for example, knowledge of copper smelting led to the discovery of iron smelting.

In the Americas production in the Old Copper Complex, located in present day Michigan and Wisconsin, was dated back to between 6000 to 3000 BC.[7]

Bronze Age

Alloying of copper with zinc or tin to make brass or bronze was practiced soon after the discovery of copper itself. There exist copper and bronze artifacts from Sumerian cities that date to 3000 BC,[8] and Egyptian artifacts of copper and copper-tin alloys nearly as old. In one pyramid, a copper plumbing system was found that is 5000 years old.[9] The Egyptians found that adding a small amount of tin made the metal easier to cast, so copper-tin (bronze) alloys were found in Egypt almost as soon as copper was found. Very important sources of copper in the Levant were located in Timna valley (Negev, now in southern Israel) and Faynan (biblical Punon, Jordan).[10]

By 2000 BC, Europe was using bronze.[8] The use of bronze became so widespread in Europe approximately from 2500 BC to 600 BC that it has been named the Bronze Age. The transitional period in certain regions between the preceding Neolithic period and the Bronze Age is termed the Chalcolithic ("copper-stone"), with some high-purity copper tools being used alongside stone tools. Brass (copper-zinc alloy) was known to the Greeks, but only became a significant supplement to bronze during the Roman empire.

During the Bronze Age, one copper mine at Great Orme in North Wales, extended for a depth of 70 meters.[11] At Alderley Edge in Cheshire, carbon dates have established mining at around 2280 to 1890 BC (at 95% probability).[12]

Antiquity and Middle Ages

In alchemy the symbol for copper, perhaps a stylized mirror, was also the symbol for the goddess and planet Venus.
Chalcolithic copper mine in Timna Valley, Negev Desert, Israel.

In Greek the metal was known by the name chalkos (χαλκός). Copper was a very important resource for the Romans, Greeks and other ancient peoples. In Roman times, it became known as aes Cyprium (aes being the generic Latin term for copper alloys such as bronze and other metals, and Cyprium because so much of it was mined in Cyprus). From this, the phrase was simplified to cuprum, hence the English copper. Copper was associated with the goddess Aphrodite/Venus in mythology and alchemy, owing to its lustrous beauty, its ancient use in producing mirrors, and its association with Cyprus, which was sacred to the goddess. In astrology, alchemy the seven heavenly bodies known to the ancients were associated with seven metals also known in antiquity, and Venus was assigned to copper.[13]

Britain's first use of brass occurred around the 3rd - 2nd century B.C. In North America, copper mining began with marginal workings by Native Americans. Native copper is known to have been extracted from sites on Isle Royale with primitive stone tools between 800 and 1600.[14]

Copper metallurgy was flourishing in South America, particularly in Peru around the beginning of the first millennium AD. Copper technology proceeded at a much slower rate on other continents. Africa's major location for copper reserves is Zambia. Copper burial ornamentals dated from the 15th century have been uncovered, but the metal's commercial production did not start until the early 1900s. Australian copper artifacts exist, but they appear only after the arrival of the Europeans; the aboriginal culture apparently did not develop their own metallurgical abilities.

Crucial in the metallurgical and technological worlds, copper has also played an important cultural role, particularly in currency. Romans in the 6th through 3rd centuries B.C. used copper lumps as money. At first, just the copper itself was valued, but gradually the shape and look of the copper became more important. Julius Caesar had his own coins, made from a copper-zinc alloy, while Octavianus Augustus Caesar's) coins were made from Cu-Pb-Sn alloys.

The gates of the Temple of Jerusalem used Corinthian bronze made by depletion gilding. Corinthian bronze was most prevalent in Alexandria, where alchemy is thought to have begun.[15] In ancient India (before 1000 B.C.), copper was used in the holistic medical science Ayurveda for surgical instruments and other medical equipment. Ancient Egyptians (~2400 B.C.) used copper for sterilizing wounds and drinking water, and as time passed, (~1500 B.C.) for headaches, burns, and itching. Hippocrates (~400 B.C.) used copper to treat leg ulcers associated with varicose veins. Ancient Aztecs fought sore throats by gargling with copper mixtures.

Copper is also the part of many rich stories and legends, such as that of Iraq's Baghdad Battery. Copper cylinders soldered to lead, which date back to 248 B.C. to 226 A.D, resemble a galvanic cell, leading people to believe this may have been the first battery. This claim has so far not been substantiated.

The Bible also refers to the importance of copper: "Men know how to mine silver and refine gold, to dig iron from the earth and melt copper from stone" (Job. 28:1-2).

Modern period

Miners at the Tamarack Mine in Copper Country, Michigan, USA in 1905

Throughout history, copper's use in art has extended far beyond currency. Vannoccio Biringuccio, Giorgio Vasari and Benvenuto Cellini are three Renaissance sculptors from the mid 1500s, notable for their work with bronze. From about 1560 to about 1775, thin sheets of copper were commonly used as a canvas for paintings. Silver plated copper was used in the pre-photograph known as the daguerreotype. The Statue of Liberty, dedicated on October 28, 1886, was constructed of copper thought to have come from French-owned mines in Norway.

Plating was a technology that began started in the mid 1600s in some areas. One common use for copper plating, widespread in the 1700s, was the sheathing of ships' hulls. Copper sheathing could be used to protect wooden hulled ships from algae, and from the shipworm "toredo", a saltwater clam. The ships of Christopher Columbus were among the earliest to have this protection.[16]

In 1801 Paul Revere established America's first copper rolling mill in Canton, Massachusetts. In the early 1800s, it was discovered that copper wire could be used as a conductor, but it wasn't until 1990 that copper, in oxide form, was discovered for use as a superconducting material. The German scientist Gottfried Osann invented powder metallurgy of copper in 1830 while determining the metal's atomic weight. Around then it was also discovered that the amount and type of alloying element (e.g. tin) would affect the tones of bells, allowing for a variety of rich sounds, leading to bell casting, another common use for copper and its alloys.

The Norddeutsche Affinerie in Hamburg was the first modern electroplating plant starting its production in 1876.[17]

Flash smelting, was developed by Outokumpu in Finland and first applied at the Harjavalta plant in 1949. The process makes smelting more energy efficient and is today used for 50% of the world’s primary copper production.[18]

Copper has been pivotal in the economic and sociological worlds, notably disputes involving copper mines. The 1906 Cananea Strike in Mexico dealt with issues of work organization. The Teniente copper mine (1904-1951) raised political issues about capitalism and class structure. Japan's largest copper mine, the Ashio mine, was the site of a riot in 1907. The Arizona miners' strike of 1938 dealt with American labor issues including the "right to strike".

Characteristics

Color

Copper just above its melting point keeps its pink luster color when enough light outshines the orange incandescence color.

Copper has a reddish, orangish, or brownish color because a thin layer of tarnish (including oxides) gradually forms on its surface when gases (especially oxygen) in the air react with it. But pure copper, when fresh, is actually a pinkish or peachy metal. Copper, caesium and gold are the only three elemental metals with a natural color other than gray or silver.[19] The usual gray color of metals depends on their "electron sea" that is capable of absorbing and re-emitting photons over a wide range of frequencies. Copper has its characteristic color because of its unique band structure. By Madelung's rule the 4s subshell should be filled before electrons are placed in the 3d subshell but copper is an exception to the rule with only one electron in the 4s subshell instead of two. The energy of a photon of blue or violet light is sufficient for a d band electron to absorb it and transition to the half-full s band. Thus the light reflected by copper is missing some blue/violet components and appears red. This phenomenon is shared with gold which has a corresponding 5s/4d structure.[20] In its liquefied state, a pure copper surface without ambient light appears somewhat greenish, a characteristic shared with gold. When liquid copper is in bright ambient light, it retains some of its pinkish luster. When copper is burnt in oxygen it gives off a black oxide.

Group 11 of the periodic table

Copper occupies the same family of the periodic table as silver and gold, since they each have one s-orbital electron on top of a filled electron shell which forms metallic bonds. This similarity in electron structure makes them similar in many characteristics. All have very high thermal and electrical conductivity, and all are malleable metals. Among pure metals at room temperature, copper has the second highest electrical and thermal conductivity, after silver.[21]

Occurrence

Native copper (~ 4 cm in size)

Copper can be found as native copper in mineral form (for example, in Michigan's Keewenaw Peninsula). It is a polycrystal, with the largest single crystals measuring 4.4x3.2x3.2 cm3.[22] Minerals such as the sulfides: chalcopyrite (CuFeS2), bornite (Cu5FeS4), covellite (CuS), chalcocite (Cu2S) are sources of copper, as are the carbonates: azurite (Cu3(CO3)2(OH)2) and malachite (Cu2CO3(OH)2) and the oxide: cuprite (Cu2O).[21]

Mechanical properties

Copper is easily worked, being both ductile and malleable. The ease with which it can be drawn into wire makes it useful for electrical work in addition to its excellent electrical properties. Copper can be machined, although it is usually necessary to use an alloy for intricate parts, such as threaded components, to get really good machinability characteristics. Good thermal conduction makes it useful for heatsinks and in heat exchangers. Copper has good corrosion resistance, but not as good as gold. It has excellent brazing and soldering properties and can also be welded, although best results are obtained with gas metal arc welding.[23]

Copper is normally supplied, as with nearly all metals for industrial and commercial use, in a fine grained polycrystalline form. Polycrystalline metals have greater strength than monocrystalline forms, and the difference is greater for smaller grain (crystal) sizes. The reason is due to the inability of stress dislocations in the crystal structure to cross the grain boundaries.[24]

Electrical properties

Copper electrical busbars distributing power to a large building.

At 59.6 × 106 S/m copper has the second highest electrical conductivity of any element, just after silver. This high value is due to virtually all the valence electrons (one per atom) taking part in conduction. The resulting free electrons in the copper amount to a huge charge density of 13.6x109 C/m3. This high charge density is responsible for the rather slow drift velocity of currents in copper cable (drift velocity may be calculated as the ratio of current density to charge density). For instance, at a current density of 5x106 A/m2 (typically, the maximum current density present in household wiring and grid distribution) the drift velocity is just a little over ⅓ mm/s.[25]

Corrosion

Pure water and air/oxygen

The Pourbaix diagram for copper in pure water, or acidic or alkali conditions. It can be seen that copper in neutral water is more noble than hydrogen.

Copper is a metal that does not react with water (H2O), but the oxygen of the air will react slowly at room temperature to form a layer of brown-black copper oxide on copper metal. Therefore Copper is denoted as semi-noble metal.

It is important to note that in contrast to the oxidation of iron by wet air that the layer formed by the reaction of air with copper has a protective effect against further corrosion. On old copper roofs a green layer of copper carbonate, called verdigris, can often be seen. A notable example of this is on the Statue of Liberty.

In contact with other metals

Copper should not be in direct mechanical contact with metals of different electropotential (for example, a copper pipe joined to an iron pipe), especially in the presence of moisture, as the completion of an electrical circuit (for instance through the common ground) will cause the juncture to act as an electrochemical cell (like a single cell of a battery). The weak electrical currents themselves are harmless but the electrochemical reaction will cause the conversion of the iron to other compounds, eventually destroying the functionality of the union. This problem is usually solved in plumbing by separating copper pipe from iron pipe with some non-conducting segment (usually plastic or rubber).

Sulfide media

The Pourbaix diagram for copper in water containing sulfide

Copper metal reacts with hydrogen sulfide- and sulfide-containing solutions, forming a series of different copper sulfides on its surface.

The Pourbaix diagram is very complex due to the existence of many different sulfides. In sulfide-containing solutions copper is less noble than hydrogen and will corrode. This can be observed in everyday life when copper metal surfaces tarnish after exposure to air containing sulfur compounds.

Ammonia media

The Pourbaix diagram for copper in 10 M ammonia solution

Copper is slowly dissolved in oxygen-containing ammonia solutions because the ammonia forms water-soluble copper complexes. The formation of these complexes causes the corrosion to become more thermodynamically favored than the corrosion of copper in an identical solution that does not contain the ammonia.

Chloride media

The Pourbaix diagram for copper in a chloride solution

Copper reacts with a combination of oxygen and hydrochloric acid to form a series of copper chlorides. Copper(II) chloride (green/blue) when boiled with copper metal undergoes a symproportionation reaction to form white copper(I) chloride.

Germicidal effect

Copper is germicidal, via the oligodynamic effect. For example, brass doorknobs disinfect themselves of many bacteria within a period of eight hours.[26] Antimicrobial properties of copper are effective against MRSA,[27] Escherichia coli[28] and other pathogens.[29][30][31] In colder temperature, longer time is required to kill bacteria.

Copper has the intrinsic ability to kill a variety of potentially harmful pathogens. On February 29, 2008, the United States EPA registered 275 alloys, containing greater than 65% nominal copper content, as antimicrobial materials[32]. Registered alloys include pure copper, an assortment of brasses and bronzes, and additional alloys. EPA-sanctioned tests using Good Laboratory Practices were conducted in order to obtain several antimicrobial claims valid against: methicillin-resistant Staphylococcus aureus (MRSA), Enterobacter aerogenes, Escherichia coli O157: H7 and Pseudomonas aeruginosa. The EPA registration allows the manufacturers of these copper alloys to legally make public health claims as to the health effects of these materials. Several of the aforementioned bacteria are responsible for a large portion of the nearly two million hospital-acquired infections contracted each year in the United States[33]. Frequently touched surfaces in hospitals and public facilities harbor bacteria and increase the risk for contracting infections. Covering touch surfaces with copper alloys can help reduce microbial contamination associated with hospital-acquired-infections on these surfaces.

Isotopes

Copper has 29 distinct isotopes ranging in atomic mass from 52 to 80. Two of these, 63Cu and 65Cu, are stable and occur naturally, with 63Cu comprising approximately 69% of naturally occurring copper.[34]

The other 27 isotopes are radioactive and do not occur naturally. The most stable of these is 67Cu with a half-life of 61.83 hours. The least stable is 54Cu with a half-life of approximately 75 ns. Unstable copper isotopes with atomic masses below 63 tend to undergo β+ decay, while isotopes with atomic masses above 65 tend to undergo β decay. 64Cu decays by both β+ and β.[34]

68Cu, 69Cu, 71Cu, 72Cu, and 76Cu each have one metastable isomer. 70Cu has two isomers, making a total of 7 distinct isomers. The most stable of these is 68mCu with a half-life of 3.75 minutes. The least stable is 69mCu with a half-life of 360 ns.[34]

Production

Chuquicamata (Chile). The largest open pit copper mines in the world.
Copper output in 2005

Output

Most copper ore is mined or extracted as copper sulfides from large open pit mines in porphyry copper deposits that contain 0.4 to 1.0 percent copper. Examples include: Chuquicamata in Chile and El Chino Mine in New Mexico. The average abundance of copper found within crustal rocks is approximately 68 ppm by mass, and 22 ppm by atoms. In 2005, Chile was the top mine producer of copper with at least one-third world share followed by the USA, Indonesia and Peru, reports the British Geological Survey.[21]

Reserves

World production trend
Copper Prices 2003 - 2008 in USD

Copper has been in use at least 10,000 years, but more than 95 percent of all copper ever mined and smelted has been extracted since 1900. Like fossil fuels, copper is a finite resource. The Earth has an estimated 61 years of copper reserves remaining. Environmental analyst, Lester Brown, however, has suggested copper might run out within 25 years based on a reasonable extrapolation of 2% growth per year.[35]

As consumption in India and China increases, copper supplies are becoming scarcer.[36] The copper price has quintupled from the 60-year low in 1999, rising from US$0.60 per pound (US$1.32/kg) in June 1999 to US$3.75 per pound (US$8.27/kg) in May 2006, where it dropped to US$2.40 per pound (US$5.29/kg) in February 2007 then rebounded to US$3.50 per pound (US$7.71/kg = £3.89 = 5.00) in April 2007.[37] By early February 2009, however, weakening global demand and a steep fall in commodity prices since the previous year's highs had left copper prices at US$1.51 per pound.[38] Production is expected to reach a peak at some point in the future and decline thereafter, according to the Hubbert peak theory.

The Intergovernmental Council of Copper Exporting Countries (CIPEC), defunct since 1992, once tried to play a similar role for copper as OPEC does for oil, but never achieved the same influence, not least because the second-largest producer, the United States, was never a member. Formed in 1967, its principal members were Chile, Peru, Zaire, and Zambia.

Methods

Applications

Copper is malleable and ductile and is a good conductor of both heat and electricity.

The purity of copper is expressed as 4N for 99.99% pure or 7N for 99.99999% pure. The numeral gives the number of nines after the decimal point when expressed as a decimal (e.g. 4N means 0.9999, or 99.99%). Copper is often too soft for its applications, so it is incorporated in numerous alloys. For example, brass is a copper-zinc alloy, and bronze is a copper-tin alloy.[39]

It is used extensively, in products such as:

Piping

  • including water supply.
Assorted copper fittings.

Electrical applications

Copper roof on the Minneapolis City Hall, coated with Patina

Architecture / Industry

Old copper utensils in a Jerusalem restaurant
  • Copper is used to prevent a building being directly struck by lightning. High above the roof, copper spikes (lightning rods) are connected to a very thick copper cable which leads to a large metal plate underneath the ground. The voltage is dispersed throughout the ground harmlessly, instead of destroying the main structure.[41]

Household products

Coinage

Biomedical applications

Chemical applications

Other

Alloys

Numerous copper alloys exist, many with important historical and contemporary uses. Speculum metal and bronze are alloys of copper and tin. Brass is an alloy of copper and zinc. Monel metal, also called cupronickel, is an alloy of copper and nickel. While the metal "bronze" usually refers to copper-tin alloys, it also is a generic term for any alloy of copper, such as aluminium bronze, silicon bronze, and manganese bronze. Copper is one of the most important constituents of carat silver and gold alloys and carat solders used in the jewelry industry, modifying the color, hardness and melting point of the resulting alloys.[48]

Compounds

Copper (I) Oxide powder

Common oxidation states of copper include the less stable copper(I) state, Cu+; and the more stable copper(II) state, Cu2+, which forms blue or blue-green salts and solutions. Under unusual conditions, a 3+ state and even an extremely rare 4+ state can be obtained. Using old nomenclature for the naming of salts, copper(I) is called cuprous, and copper(II) is cupric. In oxidation copper is mildly basic.

Copper(II) carbonate is green from which arises the unique appearance of copper-clad roofs or domes on some buildings. Copper(II) sulfate forms a blue crystalline pentahydrate which is perhaps the most familiar copper compound in the laboratory. It is used as a fungicide, known as Bordeaux mixture.

There are two stable copper oxides, copper(II) oxide (CuO) and copper(I) oxide (Cu2O). Copper oxides are used to make yttrium barium copper oxide (YBa2Cu3O7-δ) or YBCO which forms the basis of many unconventional superconductors.

  • Copper(III) compounds, rare: potassium hexafluorocuprate (K3CuF6)
  • Copper(IV) compounds, extremely rare: caesium hexafluorocuprate (Cs2CuF6)

Tests for copper(II) ion

Adding an aqueous solution of sodium hydroxide will form a blue precipitate of copper(II) hydroxide. The ionic equation is:

Cu2+ (aq) + 2 OH (aq) → Cu(OH)2 (s)

The full equation shows that the reaction is due to hydroxide ions deprotonating the hexaaquacopper(II) complex:

[Cu(H2O)6]2+ (aq) + 2 OH(aq) → Cu(H2O)4(OH)2 (s) + 2 H2O (l)

Adding ammonium hydroxide (aqueous ammonia) causes the same precipitate to form. Upon adding excess ammonia, the precipitate dissolves, forming a deep blue ammonia complex, tetraamminecopper(II):

Cu(H2O)4(OH)2 (s) + 4 NH3 (aq) → [Cu(H2O)2(NH3)4]2+ (aq) + 2 H2O (l) + 2 OH (aq)

A more delicate test than ammonia is potassium ferrocyanide, which gives a brown precipitate with copper salts.

Biological role

Rich sources of Copper include oysters, beef or lamb liver, Brazil nuts, blackstrap molasses, cocoa, and black pepper. Good sources include lobster, nuts and sunflower seeds, green olives, avocados and wheat bran.

Copper is essential in all plants and animals. The human body normally contains copper at a level of about 1.4 to 2.1 mg for each kg of body weight.[49] Copper is distributed widely in the body and occurs in liver, muscle and bone. Copper is transported in the bloodstream on a plasma protein called ceruloplasmin. When copper is first absorbed in the gut it is transported to the liver bound to albumin. Copper metabolism and excretion is controlled delivery of copper to the liver by ceruloplasmin, where it is excreted in bile.

Copper is found in a variety of enzymes, including the copper centers of cytochrome c oxidase and the enzyme superoxide dismutase (containing copper and zinc). In addition to its enzymatic roles, copper is used for biological electron transport. The blue copper proteins that participate in electron transport include azurin and plastocyanin. The name "blue copper" comes from their intense blue color arising from a ligand-to-metal charge transfer (LMCT) absorption band around 600 nm.

Most molluscs and some arthropods such as the horseshoe crab use the copper-containing pigment hemocyanin rather than iron-containing hemoglobin for oxygen transport, so their blood is blue when oxygenated rather than red.[50]

It is believed that zinc and copper compete for absorption in the digestive tract so that a diet that is excessive in one of these minerals may result in a deficiency in the other. The RDA for copper in normal healthy adults is 0.9 mg/day. On the other hand, professional research on the subject recommends 3.0 mg/day.[51] Because of its role in facilitating iron uptake, copper deficiency can often produce anemia-like symptoms. In humans, the symptoms of Wilson's disease are caused by an accumulation of copper in body tissues.

Reference ranges for blood tests, comparing blood content of copper (shown in light blue in middle) with other constituents.

Chronic copper depletion leads to abnormalities in metabolism of fats, high triglycerides, non-alcoholic steatohepatitis (NASH), fatty liver disease and poor melanin and dopamine synthesis causing depression and sunburn. Food rich in copper should be eaten away from any milk or egg proteins as they block absorption.

Toxicity

Toxicity can occur from eating acidic food that has been cooked with copper cookware. Cirrhosis of the liver in children (Indian Childhood Cirrhosis) has been linked to boiling milk in copper cookware. The Merck Manual states that recent studies suggest that a genetic defect is associated with this cirrhosis.[52] Since copper is actively excreted by the normal body, chronic copper toxicosis in humans without a genetic defect in copper handling has not been demonstrated.[53] However, large amounts (gram quantities) of copper salts taken in suicide attempts have produced acute copper toxicity in normal humans. Equivalent amounts of copper salts (30 mg/kg) are toxic in animals[54]

Miscellaneous hazards

The metal, when powdered, is a fire hazard. At concentrations higher than 1 mg/L, copper can stain clothes and items washed in water.

See also

References

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  10. ^ J.M. Tebes (2007). "A Land whose Stones are Iron, and out of whose Hills You can Dig Copper: The Exploitation and Circulation of Copper in the Iron Age Negev and Edom". DavarLogos 6 (1). http://dialnet.unirioja.es/servlet/articulo?codigo=2314512. 
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  18. ^ "Outokumpu Flash Smelting". Outokumpu. 2. http://www.outokumpu.com/files/Technology/Documents/Newlogobrochures/FlashSmelting.pdf. 
  19. ^ *Chambers, William; Chambers, Robert (1884). Chambers's Information for the People. L (5th ed.). W. & R. Chambers. p. 312. http://books.google.com/books?id=eGIMAAAAYAAJ. .
  20. ^ M. Razeghi (2006). Fundamentals of Solid State Engineering. Birkhäuser. pp. 154-156. ISBN 0387281525. 
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  22. ^ P. C. Rickwood (1981). "The largest crystals". American Mineralogist 66: 885-907. http://www.minsocam.org/ammin/AM66/AM66_885.pdf. 
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  24. ^ William F. Smith, Javad Hashemi (2003). Foundations of Materials Science and Engineering. McGraw-Hill Professional. p. 223. ISBN 0072921943. 
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  26. ^ P. J. Kuhn (1983). "Doorknobs: A Source of Nosocomial Infection?". http://members.vol.at/schmiede/MsgverSSt.html. Retrieved on 2007-08-15. 
  27. ^ Noyce JO, Michels H, Keevil CW (2006). "Potential use of copper surfaces to reduce survival of epidemic meticillin-resistant Staphylococcus aureus in the healthcare environment". J. Hosp. Infect. 63 (3): 289–97. doi:10.1016/j.jhin.2005.12.008. PMID 16650507. 
  28. ^ Noyce JO, Michels H, Keevil CW (2006). "Use of copper cast alloys to control Escherichia coli O157 cross-contamination during food processing". Appl. Environ. Microbiol. 72 (6): 4239–44. doi:10.1128/AEM.02532-05. PMID 16751537. 
  29. ^ Mehtar S, Wiid I, Todorov SD (2008). "The antimicrobial activity of copper and copper alloys against nosocomial pathogens and Mycobacterium tuberculosis isolated from healthcare facilities in the Western Cape: an in-vitro study". J. Hosp. Infect. 68 (1): 45–51. doi:10.1016/j.jhin.2007.10.009. PMID 18069086. 
  30. ^ Gant VA, Wren MW, Rollins MS, Jeanes A, Hickok SS, Hall TJ (2007). "Three novel highly charged copper-based biocides: safety and efficacy against healthcare-associated organisms". J. Antimicrob. Chemother. 60 (2): 294–9. doi:10.1093/jac/dkm201. PMID 17567632. 
  31. ^ Noyce JO, Michels H, Keevil CW (2007). "Inactivation of influenza A virus on copper versus stainless steel surfaces". Appl. Environ. Microbiol. 73 (8): 2748–50. doi:10.1128/AEM.01139-06. PMID 17259354. 
  32. ^ "EPA registers copper-containing alloy products". US Environmental Protection Agency. http://www.epa.gov/pesticides/factsheets/copper-alloy-products.htm. Retrieved on 2009-06-06. 
  33. ^ "Center for Decease Control and Prevention". http://www.cdc.gov/ncidod/eid/vol7no2/pdfs/peterson.pdf. Retrieved on 2009-06-06. 
  34. ^ a b c Audi, G (2003). "Nubase2003 Evaluation of Nuclear and Decay Properties". Nuclear Physics A (Atomic Mass Data Center) 729: 3–128. doi:10.1016/j.nuclphysa.2003.11.001. 
  35. ^ Brown, Lester (2006). Plan B 2.0: Rescuing a Planet Under Stress and a Civilization in Trouble. New York: W.W. Norton. p. 109. ISBN 0393328317. 
  36. ^ Andrew Leonard (2006-03-02). "Peak copper?". Salon - How the World Works. http://www.salon.com/tech/htww/2006/03/02/peak_copper/index.html. Retrieved on 2008-03-23. 
  37. ^ "Copper Trends: Live Metal Spot Prices". http://metalspotprice.com/copper-trends/. 
  38. ^ R. Ackerman (02-04-2009). "A Bottom In Sight For Copper". Forbes. http://www.forbes.com/2009/02/04/copper-frontera-southern-markets-equity-0205_china_51.html. 
  39. ^ "Copper". American Elements. 2008. http://www.americanelements.com/cu.html. Retrieved on 2008-07-12. 
  40. ^ Berg, Jan. "Why did we paint the library's roof?". http://www.deforest.lib.wi.us/FAQS.htm. Retrieved on 2007-09-20. 
  41. ^ Physics 1, Jacaranda Science. 3rd Ed.. 2009. 
  42. ^ "The Euro - Born out of Copper". Copper Development Association. http://www.cda.org.uk/news/euro.htm. Retrieved on 2008-07-12. 
  43. ^ a b "Coin Specifications". United States Mint. 2008. http://www.usmint.gov/about_the_mint/index.cfm?flash=yes&action=coin_specifications. Retrieved on 2008-07-12. 
  44. ^ "Demonetisation". The Royal Mint. 2008-07-01. http://www.royalmint.com/Corporate/BritishCoinage/Demonetisation.aspx. Retrieved on 2008-07-13. 
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Further reading

External links


 
Translations: Copper
Top

Dansk (Danish)
1.
n. - kobber, kobbermønt, gruekedel, plettet ildfugl
v. tr. - forkobre

idioms:

  • copper beech    blodbøg

2.
n. - [sl] politibetjent, strisser

Nederlands (Dutch)
(rood)koper, (mv) kopergeld, koperkleurig, ketel, koperen, politieagent, vuurvlinder, verkoperen

Français (French)
1.
n. - (Chim) cuivre, couleur cuivre, (GB) petite monnaie, (GB, Hist) lessiveuse
v. tr. - enduire, couvrir, ou protéger de cuivre

idioms:

  • copper beech    hêtre pourpre

2.
n. - agent de police, flic (fam)

Deutsch (German)
1.
n. - Kupfer, Kupfermünze, Kupferkessel
v. - verkupfern, mit Kupfer beschlagen

idioms:

  • copper beech    Blutbuche, Rotbuche

2.
n. - Polizist

Ελληνική (Greek)
n. - χαλκός (κν. μπακίρι), (καθομ.) αστυνομικός, μπάτσος
adj. - χάλκινος

idioms:

  • copper beech    κόκκινη οξιά

Italiano (Italian)
rame, poliziotto, di rame

idioms:

  • copper beech    faggio rosso

Português (Portuguese)
n. - cobre (m), moeda (f)
adj. - de cobre

idioms:

  • copper beech    tipo de árvore (f) de faia com folhas cor de cobre

Русский (Russian)
медь, полицейский, медный, бурый

idioms:

  • copper beech    красный бук

Español (Spanish)
1.
n. - cobre, de cobre
v. tr. - cubrir con cobre

idioms:

  • copper beech    haya roja

2.
n. - agente de policía, policía

Svenska (Swedish)
n. - koppar, kopparmynt, stor kopparkittel, kopparrött, snut (sl.)
adj. - koppar-, kopparröd

中文(简体)(Chinese (Simplified))
1. 铜, 铜币, 铜制品, 红铜色, 镀铜于, 覆以铜皮

idioms:

  • copper beech    紫叶欧洲山毛榉

2. 警察

中文(繁體)(Chinese (Traditional))
1.
n. - 警察

2.
n. - 銅, 銅幣, 銅製品, 紅銅色
v. tr. - 鍍銅於, 覆以銅皮

idioms:

  • copper beech    紫葉歐洲山毛櫸

한국어 (Korean)
1.
n. - 구리, 동전, 취사용 보일러
v. tr. - 구리로 싸다, ~에 반대하여 돈을 걸다

2.
n. - 순경, 밀고자, 감형

日本語 (Japanese)
n. - 銅, 銅貨, 銅製品
adj. - 銅製の, 赤銅色の, 銅の

idioms:

  • copper beech    ヨーロッパブナ

العربيه (Arabic)
‏(الاسم) نحاس, , شرطي (صفه) نحاسي اللون, نحاسي‏

עברית (Hebrew)
n. - ‮נחושת, מטבע, פרפר שכנפיו כצבע הנחושת‬
v. tr. - ‮ציפה בנחושת‬
n. - ‮דוד-הרתחה, שוטר‬


 
 

 

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