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Scandium ( /ˈskændiəm/ SKAN-dee-əm) is a chemical element with symbol Sc and atomic number 21. A silvery-white metallic transition metal, it has historically been sometimes classified as a rare earth element, together with yttrium and the lanthanoids. In 1879, Lars Fredrik Nilson and his team, found a new element with spectral analysis, in the minerals euxenite and gadolinite from Scandinavia.

Scandium is present in most of the rare earth element and uranium deposits, but it is extracted from these ores in only a few mines worldwide. Due to the low availability and the difficulties in the preparation of metallic scandium, which was first done in 1937, it took until the 1970s before applications for scandium were developed. The positive effects of scandium on aluminium alloys were discovered in the 1970s, and its use in such alloys remains its only major application.

The properties of Sc compounds are intermediate between the properties of Al and Y, and there is a diagonal relationship between the behavior of Mg and Sc, just as there is between Be and Al. There has been controversy as to whether yttrium is in the same group as lanthanum or as lutetium.[3] In the chemical compounds of the elements shown as group 3, above, the predominant oxidation state is +3. The ions M3+ will all have the electronic configuration of a noble gas, so it is reasonable that they should be in the same group of the periodic table. Most modern text-books place Sc, Y, La and Ac in the same periodic group.

 

 

Contents

[hide]

  • 1 Properties
    • 1.1 Chemical characteristics of the element
    • 1.2 Isotopes
    • 1.3 Occurrence
  • 2 Production
  • 3 Compounds
    • 3.1 Oxides and hydroxides
    • 3.2 Halides and pseudohalides
    • 3.3 Organic derivatives
    • 3.4 Compounds where scandium is not Sc3+
  • 4 History
  • 5 Applications
  • 6 Health and safety
  • 7 See also
  • 8 References
  • 9 External links

[edit] Properties

[edit] Chemical characteristics of the element

Scandium metal is hard and has a silvery appearance. It develops a slightly yellowish or pinkish cast when exposed to air. It is not resistant to weathering and dissolves slowly in most dilute acids. It does not react with a 1:1 mixture of nitric acid (HNO3) and hydrofluoric acid, HF, presumably due to the formation of an impermeable passive layer on the surface of the metal.

[edit] Isotopes

Main article: Isotopes of scandium

Scandium exists naturally as a single isotope 45Sc, which has a nuclear spin of 7/2. Thirteen radioisotopes have been characterized with the most stable being 46Sc with a half-life of 83.8 days, 47Sc with a half-life of 3.35 days, and 48Sc with a half-life of 43.7 hours. All of the remaining radioactive isotopes have half lives that are less than 4 hours, and the majority of these have half-lives that are less than 2 minutes. This element also has five meta states with the most stable being 44mSc (t½ = 58.6 h).[4]

The isotopes of scandium range in atomic weight from 40 u (40Sc) to 54 u (54Sc). The primary decay mode at masses lower than the only stable isotope, 45Sc, is electron capture, and the primary mode at masses above it is beta emission. The primary decay products at atomic weights below 45Sc are calcium isotopes and the primary products from higher atomic weights are titanium isotopes.[4]

[edit] Occurrence

Scandium does not have a particularly low abundance in the earth's crust. Estimates vary from 18 to 25 ppm, which is comparable to the abundance of cobalt (20–30 ppm). Scandium is only the 50th most common element on earth (35th most abundant in the crust, but it is the 23rd most common element in the sun).[5] However, scandium is distributed sparsely and occurs in trace amounts in many minerals.[6] Rare minerals from Scandinavia[7] and Madagascar[8] such as thortveitite, euxenite, and gadolinite are the only known concentrated sources of this element. Thortveitite can contain up to 45% of scandium in the form of scandium(III) oxide.[7]

The stable form of scandium is created in supernovas via the r-process.[9]

[edit] Production

World production of scandium is in the order of 2 tonnes per year in the form of scandium oxide. The primary production is 400 kg while the rest is from stockpiles of Russia generated during the Cold War. In 2003, only three mines produced scandium: the uranium and iron mines in Zhovti Vody in Ukraine, the rare earth mines in Bayan Obo, China and the apatite mines in the Kola peninsula, Russia. In each case scandium is a byproduct from the extraction of other elements.[10] and is sold as scandium oxide.

The production of metallic scandium is in the order of 10 kg per year.[10][11] The oxide is converted to scandium fluoride and reduced with metallic calcium.

Madagascar and Iveland-Evje region in Norway have the only deposits of minerals with high scandium content, thortveitite (Sc,Y)2(Si2O7) and kolbeckite ScPO4·2H2O, but these are not being exploited.[11] Other scandium sources include the nickel and cobalt laterite mines in Australia at Greenvale, Queensland, Syerston and Lake Innes, New South Wales, iron, tin, and tungsten deposits in China and uranium deposits in Russia and Kazakhstan. As of 2003, scandium was not being extracted from the tailings at any of these mines, but some scandium extraction may be started if there is sufficient demand.[10] There is currently no primary production of scandium in the Americas, Europe, or Australia.

The absence of reliable, secure, stable and long term production has limited commercial applications of scandium in most countries. This is despite a comprehensive body of research and a large number of patents which identify significant benefits for the use of scandium over other elements. Particularly promising are the properties of stabilizing zirconia and strengthening aluminium alloys (0.5% scandium). Scandia-stabilized zirconia has a growing market demand for use as a high efficiency electrolyte in solid oxide fuel cells. The availability of high-purity scandium oxide production is proposed to commence from the NORNICO project near Greenvale, Queensland in 2013–2014.

[edit] Compounds

The chemistry is almost completely dominated by the trivalent ion. The radii of M3+ ions in the preceding table indicate why the chemistry of scandium is more closely related to that of yttrium than that of aluminium and explains why scandium has been classified as a lanthanide-like element.

 

Ionic radii (pm)

Al Sc Y La Lu

53.5 74.5 90.0 103.2 86.1

[edit] Oxides and hydroxides

The oxide Sc2O3 is weakly acidic and the hydroxide Sc(OH)3 is amphoteric:

 

Sc(OH)3 + 3 OH− → Sc(OH)3−

6Sc(OH)3 + 3 H+ + 3 H2O → [Sc(H2O)6]3+

The α- and γ- forms of scandium oxide hydroxide (ScO(OH)), are isostructural with their aluminium oxide hydroxide counterparts.[12] Solutions of Sc3+ in water are acidic because of hydrolysis.

[edit] Halides and pseudohalides

The halides ScX3 (X = Cl, Br, I) are very soluble in water, but ScF3 is insoluble. In all four halides the scandium is 6-coordinate. The halides are Lewis acids; for example, ScF3 dissolves a solution containing excess fluoride to form [ScF6]3−. The coordination number 6 is typical of Sc(III). In the larger Y3+ and La3+ ions, 8- and 9- coordination are often found. Scandium(III) triflate is sometimes used as a Lewis acid catalyst in organic chemistry.

[edit] Organic derivatives

Main article: Organoscandium compounds

Scandium forms a series of organometallic compounds with C5Me5 ligands (Cp) such as the chlorine-bridged dimer, [ScCp2Cl]2.[13]

[edit] Compounds where scandium is not Sc3+

Compounds that feature Sc in the oxidation state other than 3 are well known. The cluster [Sc6Cl12]3− is a similar structure to that of the Nb6Cl12 cluster wherein chloride centers bridge the 12 edges of an octahedron of metal atoms.[14] The nature of the hydride ScH2 is not yet fully understood.[2] It appears not to be a saline hydride of Sc(II), but may be a compound of Sc(III) with two hydrides and an electron which is delocalized in a kind of metallic structure. ScH can be observed spectroscopically at high temperatures in the gas phase.[1] In the compounds ScB and ScC, boron and carbon are incorporated non-stoichiometrically into the lattice of the scandium.[15]

[edit] History

Dmitri Mendeleev, creator of the periodic table, predicted the existence of an element ekaboron, with an atomic mass between 40 and 48 in 1869. Ten years later Lars Fredrik Nilson found a new element in the minerals euxenite and gadolinite from Scandinavia. He was able to prepare 2 grams of scandium oxide of high purity.[16][17] He named it scandium, from the Latin Scandia meaning "Scandinavia". Nilson was apparently unaware of Mendeleev's prediction, but Per Teodor Cleve recognized the correspondence and notified Mendeleev.[18]

Metallic scandium was produced for the first time in 1937 by electrolysis of a eutectic mixture, at 700–800 °C, of potassium, lithium, and scandium chlorides.[19] The first pound of 99% pure scandium metal was produced in 1960. The use for aluminium alloys began in 1971, following a US patent.[20] Aluminium-scandium alloys were also developed in the USSR.[21]

[edit] Applications

 

 

 

 

Parts of the MiG-29 are made from Al-Sc alloy.[22]

The addition of scandium to aluminium limits the excessive grain growth that occurs in the heat-affected zone of welded aluminium components. This has two beneficial effects: the precipitated Al3Sc forms smaller crystals than are formed in other aluminium alloys[22] and the volume of precipitate-free zones that normally exist at the grain boundaries of age-hardening aluminium alloys is reduced.[22] Both of these effects increase the usefulness of the alloy. However, titanium alloys, which are similar in lightness and strength, are cheaper and much more widely used.[23]

The main application of scandium by weight is in aluminium-scandium alloys for minor aerospace industry components. These alloys contain between 0.1% and 0.5% of scandium. They were used in the Russian military aircraft, specifically the MiG-21 and MiG-29.[22]

Some items of sports equipment, which rely on high performance materials, have been made with scandium-aluminium alloys, including baseball bats[24], lacrosse sticks, as well as bicycle[25] frames and components. Lacrosse sticks are also made with scandium-titanium alloys to take advantage of the strength of titanium. The American gunmaking company Smith & Wesson produces revolvers with frames composed of scandium alloy and cylinders of titanium.[26]

Approximately 20 kg (as Sc2O3) of scandium is used annually in the United States to make high-intensity discharge lamps.[27] Scandium iodide, along with sodium iodide, when added to a modified form of mercury-vapor lamp, produces a form of metal halide lamp, an artificial light source which produce a very white light with high color rendering index that sufficiently resembles sunlight to allow good color-reproduction with TV cameras.[28] About 80 kg of scandium is used in metal halide lamps/light bulbs globally per year. The first scandium-based metal halide lamps were patented by General Electric and initially made in North America, although they are now produced in all major industrialized countries. The radioactive isotope 46Sc is used in oil refineries as a tracing agent.[27] Scandium triflate is a catalytic Lewis acid used in organic chemistry.[29]

[edit] Health and safety

Elemental scandium is not considered to be toxic. Little animal testing of scandium compounds has been done.[30] The median lethal dose (LD50) levels for scandium(III) chloride for rats have been determined and were intraperitoneal 4 mg/kg and oral 755 mg/kg.[31] In the light of these results compounds of scandium should be handled as compounds of moderate toxicity.

引用出處: 

 http://en.wikipedia.org/wiki/Scandium

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镉(gé,音隔),是一种化学元素,它的化学符号是Cd,它的原子序数是48,是一种蓝白色的过渡金属,性质柔软,有毒。镉能在锌矿中找到。镉和锌均会用作电池的材料。

纠错 编辑摘要

目录

  • 1 概述
  • 2 发现
  • 3 性质
  • 4 元素用途
  • 5 危害
  •  

  • 1 概述
  • 2 发现
  • 3 性质
  • 4 元素用途
  • 5 危害
    • 5.1 人体
    • 5.2 环境
    • 5.3 预防
  • 6 污染事件

 

 

镉 - 概述

镉和锌是同族之金属元素,往往与锌、铜、铅等共生,在冶炼铜、锌及镀镉工厂中均有相当量的镉单质和化合物排入大气与废水,废水中的镉排入江河沉积天水底并被生物吸收。

目 前,世界上主要生产镉的国家有美国、独联体、加拿大、日本、澳大利亚等国。美国是世界主要产镉的国家,1940年就已接近3000吨。1977年世界镉的 总产量已近两万吨。美国也是最大的镉进口国,其次是英国、法国和比利时。估计资本主义国家镉的消费量占世界总消费量的三分之二左右。

 

镉 - 发现

镉 与它的同族元素汞和锌相比,被发现的晚的多。它在地壳中含量比汞还多一些,但是汞一经出现就以强烈的金属光泽、较大的比重、特殊的流动性和能够溶解多种金 属的姿态吸引了人们的注意。镉在地壳中的含量比锌少得多,常常以少量包含于锌矿中,很少单独成矿。金属镉比锌更易挥发,因此在用高温炼锌时,它比锌更早逸 出,逃避了人们的觉察。这就注定了镉不可能先于锌而被人们发现。

 

镉 - 性质

镉,原子序数48,原子量112.411,元素名来源于拉丁文,原意是“菱锌矿”。镉是较稀有的元素,在地壳中的含量约为十万分之二。镉在自然界都以化合物形式存在,主要硫镉矿等。镉有8种天然同位素:镉106、108、110、111、112、113、114、116。

 

镉 为银白色有光泽金属,熔点320.9°C,沸点765°C,密度8.642克/厘米³。比锡稍硬,比锌软,有韧性和延展性。镉在干燥空气中很稳定,湿空气 中表面覆盖氧化膜,红热时形成褐色氧化物,燃烧时产生红色火焰;镉与卤素在高温下反应剧烈,形成卤化镉;可与硫直接化合成硫化镉;能溶于酸形成相应的盐, 但不溶于强碱。

 

镉 - 元素用途

用于电底、制造合金等;并可做成原子反应堆中的中子吸收棒。镉氧化电位高,故可用作铁、钢、铜之保护膜,广用于电镀上,并用于充电电池、电视映像管、黄色颜料及作为塑料之安定剂。镉化合物可用于杀虫剂、杀菌剂、颜料、油漆等之制造业。

 

镉 - 危害

人体

镍镉电池

镉不是人体所必需的微量元素。新生婴儿体内几乎无镉,人体中镉全部是出生后通过外界环境(例如饮水、食物、香烟)进入人体的。

研究显示,镉中毒会造成肾小管再吸收障碍,低分子量蛋白质和钙质等由尿中流失,长期下去容易形成骨质软化,关节疼痛、骨折及骨骼变形等。

 

长期摄入过量的镉,会影响体内其他有益元素的效能,造成肝肾损害、肺气肿、支气管炎、内分泌失调、食欲不振、失眠等问题。镉转移至动脉,使血压上升,引致血管脂肪化。高血压病人尿中的镉含量较正常值高出40%。另外,镉也是一种致癌物质,可能诱发前列腺癌症。

加工食物会破坏镉与锌的平衡,饮食中若锌含量不足,身体便会积存镉以取代。

环境

镉 污染土壤,可造成公害病痛痛病。镉对土壤的污染,主要通过两种形式,一是工业废气中的镉随风向四周扩散,经自然沉降,蓄积于工厂周围土壤中,另一 种方式是含镉工业废水灌溉农田,使土壤受到镉的污染。因此为了防止镉对环境的污染,必须做好环境保护工作,严格执行镉的环境卫生标准。

预防

为了预防镉中毒,熔炼、使用镉及其化合物的场所,应具有良好的通风和密闭装置。焊接和电镀工艺除应有必要的排风设备外,操作时应戴个人防毒面具。不应在生产场所进食和吸烟。中国规定的生产场所氧化镉最高容许浓度为0.1mg/m3。

 

镀镉器皿不能存放食品,特别是醋类等酸性食品。高锌食物有助排除镉。此外,高钙和高硒食物亦有排镉效力。

 

镉 - 污染事件

浏阳镉污染

1、2009年8月的湖南浏阳市镇头镇镉污染,事源长沙湘和化工厂生产次氧化锌和硫酸锌但没有完善的排污设施。截止09年8月2日,该工厂被永久关闭。

2、1930-1960件代,日本富山县神通川流域部分镉污染。事源炼锌厂排放的含镉废水污染了周围的耕地和水源。

引用出處: 

 http://www.hudong.com/wiki/%E9%95%89

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Cadmium ( /ˈkædmiəm/ KAD-mee-əm) is a chemical element with the symbol Cd and atomic number 48. The soft, bluish-white metal is chemically similar to the two other metals in group 12, zinc and mercury. Similar to zinc it prefers oxidation state +2 in most of its compounds and similar to mercury it shows a low melting point compared to transition metals. Cadmium and its congeners are not considered transition metals, in that they do not have partly filled d or f electron shells in the elemental or common oxidation states.[2] Average concentration in the earth’s crust is between 0.1 and 0.5 parts per million (ppm). It was discovered simultaneously by Stromeyer and Hermann, both in Germany, as an impurity in zinc carbonate.[3]

Cadmium occurs as a minor component in most zinc ores and therefore is a byproduct of zinc production. Cadmium was used for a long time as a pigment and for corrosion resistant plating on steel. Cadmium compounds were used to stabilize plastic. With the exception of its use in nickel-cadmium batteries and cadmium telluride solar panels, the use of cadmium is generally decreasing in its other applications. These declines have been due to competing technologies, cadmium’s toxicity in certain forms and concentration and resulting regulations.[4] Although cadmium is toxic, one enzyme, a carbonic anhydrase with cadmium as reactive center has been discovered.

 

 

Contents

[hide]

  • 1 Characteristics
    • 1.1 Physical properties
    • 1.2 Chemical properties
    • 1.3 Isotopes
  • 2 History
  • 3 Occurrence
  • 4 Extraction
  • 5 Applications
    • 5.1 Batteries
    • 5.2 Other uses
    • 5.3 Historic uses
  • 6 Biological role
    • 6.1 Neurological role
  • 7 Toxicity
  • 8 Product recalls
    • 8.1 Highbury Seats
    • 8.2 Jewelry
    • 8.3 McDonald's drinking glasses
  • 9 See also
  • 10 References
  • 11 External links

[edit] Characteristics

[edit] Physical properties

Cadmium is a soft, malleable, ductile, bluish-white bivalent metal. It is similar in many respects to zinc but forms complex compounds.[5]

[edit] Chemical properties

 

See also Category: Cadmium compounds

The most common oxidation state of cadmium is +2, though rare examples of +1 can be found. Cadmium burns in air to form brown amorphous cadmium oxide (CdO). The crystalline form of the same compound is dark red and changes color when heated, similar to zinc oxide. Hydrochloric acid, sulfuric acid and nitric acid dissolve cadmium by forming cadmium chloride (CdCl2) cadmium sulfate (CdSO4) or cadmium nitrate (Cd(NO3)2). The oxidation state +1 can be reached by dissolving cadmium in a mixture of cadmium chloride and aluminium chloride, forming the Cd22+ cation, which is similar to the Hg22+ cation in mercury(I) chloride.[5]

 

Cd + CdCl2 + 2 AlCl3 → Cd2[AlCl4]2

[edit] Isotopes

 

 

 

 

The cadmium-113 total cross section clearly showing the cadmium cutoff.

Main article: Isotopes of cadmium

Naturally occurring cadmium is composed of 8 isotopes. For two of them, natural radioactivity was observed, and three others are predicted to be radioactive but their decay is not observed, due to extremely long half-life times. The two natural radioactive isotopes are 113Cd (beta decay, half-life is 7.7 × 1015 years) and 116Cd (two-neutrino double beta decay, half-life is 2.9 × 1019 years). The other three are 106Cd, 108Cd (double electron capture), and 114Cd (double beta decay); only lower limits on their half-life times have been set. At least three isotopes - 110Cd, 111Cd, and 112Cd - are stable. Among the isotopes absent in natural cadmium, the most long-lived are 109Cd with a half-life of 462.6 days, and 115Cd with a half-life of 53.46 hours. All of the remaining radioactive isotopes have half-lives that are less than 2.5 hours, and the majority of these have half-lives that are less than 5 minutes. This element also has 8 known meta states, with the most stable being 113mCd (t½ = 14.1 years), 115mCd (t½ = 44.6 days), and 117mCd (t½ = 3.36 hours).

The known isotopes of cadmium range in atomic mass from 94.950 u (95Cd) to 131.946 u (132Cd). For isotopes lighter than 112 u, the primary decay mode is electron capture and the dominant decay product is element 47 (silver). Heavier isotopes decay mostly through beta emission producing element 49 (indium).

One isotope of cadmium, 113Cd, absorbs neutrons with very high probability if they have an energy below the cadmium cut-off and transmits them readily otherwise. The cadmium cut-off is about 0.5 eV.[6] Neutrons with energy below the cutoff are deemed slow neutrons, distinguishing them from intermediate and fast neutrons.

Cadmium is created via the long S-process in low-medium mass stars (.6 -> 10 solar masses), lasting thousands of years to do. It requires a silver atom to capture a neutron and then undergo beta decay.[citation needed]

[edit] History

 

 

 

 

Friedrich Stromeyer

Cadmium (Latin cadmia, Greek καδμεία meaning "calamine", a cadmium-bearing mixture of minerals, which was named after the Greek mythological character, Κάδμος Cadmus, the founder of Thebes) was discovered simultaneously by Friedrich Stromeyer[7] and Karl Samuel Leberecht Hermann, both in Germany, as an impurity in zinc carbonate.[4] Stromeyer found the new element as an impurity in zinc carbonate (calamine), and, for 100 years, Germany remained the only important producer of the metal. The metal was named after the Latin word for calamine, since the metal was found in this zinc compound. Stromeyer noted that some impure samples of calamine changed color when heated but pure calamine did not. He was persistent in studying these results and eventually isolated cadmium metal by roasting and reduction of the sulfide. Even though cadmium and its compounds may be toxic in certain forms and concentrations, the British Pharmaceutical Codex from 1907 states that cadmium iodide was used as a medication to treat "enlarged joints, scrofulous glands,[8] and chilblains".

In 1927, the International Conference on Weights and Measures redefined the meter in terms of a red cadmium spectral line (1 m = 1,553,164.13 wavelengths).[9] This definition has since been changed (see krypton).

After the industrial scale production of cadmium started in the 1930s and 1940s the major application was the coating of iron and steel to prevent corrosion.[4] In 1944, 62% and in 1956 59% of the cadmium in the United States was used for this purpose.[10] The second application was red, orange and yellow pigments based on sulfides and selenides of cadmium. In 1956, 24% of the cadmium used within the United States was used for this purpose.[10] The stabilizing effect of cadmium-containing chemicals (carboxylates such as the laureate and the stearate) on PVC led to a increased use of those compounds in the 1970s and 1980s. The use of cadmium in applications such as pigments, coatings, stabilizers and alloys declined due to environmental and health regulations in the 1980s and 1990s. In 2006, only 7% of total cadmium consumption was used for plating and coating and only 10% was used for pigments.[4] The decrease in consumption in other applications was made up by a growing demand of cadmium in nickel-cadmium batteries, which accounted for 81% of the cadmium consumption in the United States in 2006.[11]

[edit] Occurrence

 

 

 

 

Cadmium metal

 

See also Category: Cadmium minerals

Cadmium-containing ores are rare and are found to occur in small quantities. However, traces do naturally occur in phosphate, and have been shown to transmit in food through fertilizer application.[12] Greenockite (CdS), the only cadmium mineral of importance, is nearly always associated with sphalerite (ZnS). As a consequence, cadmium is produced mainly as a byproduct from mining, smelting, and refining sulfidic ores of zinc, and, to a lesser degree, lead and copper. Small amounts of cadmium, about 10% of consumption, are produced from secondary sources, mainly from dust generated by recycling iron and steel scrap. Production in the United States began in 1907, but it was not until after World War I that cadmium came into wide use.[13][14]

One place where metallic cadmium can be found is the Vilyuy River basin in Siberia.[15]

[edit] Extraction

 

 

 

 

World production trend

 

 

 

 

Cadmium output in 2005

In 2001, China was the top producer of cadmium with almost one-sixth world share closely followed by South Korea and Japan, reports the British Geological Survey.[16]

Cadmium is a common impurity in zinc ores, and it is most often isolated during the production of zinc. Some zinc ores concentrates from sulfidic zinc ores contain up to 1.4% of cadmium.[17] In 1970s, the output of cadmium was 6.5 pounds per ton of zinc.[17] Zinc sulfide ores are roasted in the presence of oxygen, converting the zinc sulfide to the oxide. Zinc metal is produced either by smelting the oxide with carbon or by electrolysis in sulfuric acid. Cadmium is isolated from the zinc metal by vacuum distillation if the zinc is smelted, or cadmium sulfate is precipitated out of the electrolysis solution.[14][18]

[edit] Applications

[edit] Batteries

 

 

 

 

Ni-Cd batteries

In 2009, 86% of all the cadmium is used in batteries, predominantly in rechargeable nickel-cadmium batteries. Nickel-cadmium cells have a nominal cell potential of 1.2 V. The cell consists of a positive nickel hydroxide electrode and a negative cadmium electrode plate separated by an alkaline electrolyte (potassium hydroxide). The European Union banned the use of cadmium in electronics in 2004 with several exceptions but reduced the allowed content of cadmium in electronics to 0.002%.[19]

[edit] Other uses

 

 

 

 

Violet light from a helium cadmium metal vapor laser. The highly monochromatic color arises from the 441.563 nm transition line of cadmium.

 

 

 

 

Train painted with cadmium orange

 

 

 

 

A photograph and representative spectrum of photoluminescence from colloidal CdSe quantum dots.

Most of cadmium which is not consumed in battery production is used mainly for cadmium pigments, coatings and plating. Examples of some uses include:

  • In electroplating (6% cadmium).[20] Cadmium electroplating is widely used in aircraft industry due to the excellent corrosion resistance of cadmium-plated steel components. The coating is usually passivated by chromate salts.[citation needed]
  • Helium-cadmium lasers are a popular source of blue-ultraviolet laser light. They operate either at 325 or 422 nm and are used in fluorescence microscopes and various laboratory experiment.[21]
  • Cadmium is used as a barrier to control neutrons in nuclear fission.[20]
  • The pressurized water reactor designed by Westinghouse Electric Company uses an alloy consisting of 80% silver, 15% indium, and 5% cadmium.[20]
  • Cadmium oxide in black and white television phosphors and in the blue and green phosphors for color television picture tubes.[22]
  • Cadmium sulfide (CdS) as a photoconductive surface coating for photocopier drums.[23]
  • In paint pigments, cadmium forms various salts, with CdS being the most common. This sulfide is used as a yellow pigment. Cadmium selenide can be used as red pigment, commonly called cadmium red. To painters who work with the pigment, cadmium yellows, oranges, and reds are the most brilliant and long-lasting colors to use. In fact, during production, these colors are significantly toned down before they are ground with oils and binders, or blended into watercolors, gouaches, acrylics, and other paint and pigment formulations. Since these pigments are potentially toxic, it is recommended to use a barrier cream on the hands to prevent absorption through the skin when working with them[24] even though the amount of cadmium absorbed into the body through the skin is usually reported to be less than 1%.[citation needed]
  • Cadmium selenide quantum dots emit bright luminescence under UV excitation (He-Cd laser, for example). The color of this luminescence can be green, yellow or red depending on the particle size. Colloidal solutions of those particles are used for imaging of biological tissues and solutions with a fluorescence microscope.[25]
  • Cadmium is a component of some compound semiconductors, such as cadmium sulfide, cadmium selenide, and cadmium telluride, which can be used for light detection or solar cells. HgCdTe is sensitive to infrared[20] light and therefore may be utilized as an infrared detector or switch for example in remote control devices.
  • In PVC as heat, light, and weathering stabilizers[20][26] although cadmium stabilizers have now been almost completely replaced with barium-zinc, calcium-zinc and organo-tin stabilizers.
  • In molecular biology, cadmium is used to block voltage-dependent calcium channels from fluxing calcium ions, as well as in hypoxia research to stimulate proteasome-dependent degradation of Hif-1α.[27]

[edit] Historic uses

  • In many kinds of solder.[20]
  • In bearing alloys, due to a low coefficient of friction and very good fatigue resistance.[20]
  • In some of the lowest-melting alloys, such as Wood's metal.[28]

[edit] Biological role

Cadmium has no known useful role in higher organisms.[29] A role for cadmium in lower lifeforms has recently been found. A cadmium-dependent carbonic anhydrase has been found in marine diatoms. Cadmium performs the same function as zinc in other anhydrases, but the diatoms live in environments with very low zinc concentrations and thus the biological system has utilized cadmium in place of zinc to perform that function normally carried out by zinc. The discovery was made using X-ray absorption fluorescence spectroscopy (XAFS), and cadmium was characterized by noting the energy of the X-rays that were absorbed.[30]

The highest concentration of cadmium has been found to be absorbed in the kidneys of humans, and up to about 30 mg of cadmium is commonly inhaled throughout childhood and adolescence. [31][32]

[edit] Neurological role

Cadmium can be used to block calcium channels in chicken neurons. (source:"Calcium channel block by cadmium in chicken sensory neurons" -- PNAS March 1, 1989 vol. 86 no. 5 1736-1740)

[edit] Toxicity

Main article: Cadmium poisoning

 

 

 

 

WHO international poison warning symbol

The most dangerous form of occupational exposure to cadmium is inhalation of fine dust and fumes, or ingestion of highly soluble cadmium compounds.[4] Inhalation of cadmium-containing fumes can result initially in metal fume fever but may progress to chemical pneumonitis, pulmonary edema, and death.[33]

Cadmium is also a potential environmental hazard. Human exposures to environmental cadmium are primarily the result of fossil fuel combustion, phosphate fertilizers, natural sources, iron and steel production, cement production and related activities, nonferrous metals production, and municipal solid waste incineration.[4] However, there have been a few instances of general population toxicity as the result of long-term exposure to cadmium in contaminated food and water. In the decades leading up to World War II, Japanese mining operations contaminated the Jinzū River with cadmium and traces of other toxic metals. As a consequence, cadmium accumulated in the rice crops growing along the riverbanks downstream of the mines. Some members of the local agricultural communities consuming the contaminated rice developed itai-itai disease and renal abnormalities, including proteinuria and glucosuria.[34] The victims of this poisoning were almost exclusively post-menopausal women with low iron and other mineral body stores. Similar general population cadmium exposures in other parts of the world have not resulted in the same health problems as long as the populations maintained sufficient iron and other mineral levels. Thus, while cadmium is a major factor in the Itai Itai disease in Japan, most researchers have concluded that it was one of several factors.[4] Cadmium is one of six substances banned by the European Union's Restriction on Hazardous Substances (RoHS) directive, which bans certain hazardous substances in electrical and electronic equipment but allows for certain exemptions and exclusions from the scope of the law.[35]

There has been research linking exposure to cadmium to lung and prostate cancer. However, there is still a substantial controversy about the carcinogenicity of cadmium in the scientific community. More recent studies suggest that arsenic rather than cadmium may lead to the increased lung cancer mortality rates. Furthermore, most data regarding the carcinogenicity of cadmium rely on research confounded by the presence of other carcinogenic substances.[4]

Tobacco smoking is the most important single source of cadmium exposure in the general population. It has been estimated that about 10% of the cadmium content of a cigarette is inhaled through smoking. The absorption of cadmium from the lungs is much more effective than that from the gut, and as much as 50% of the cadmium inhaled via cigarette smoke may be absorbed.[36]

On average, smokers have 4-5 times higher blood cadmium concentrations and 2-3 times higher kidney cadmium concentrations than non-smokers. Despite the high cadmium content in cigarette smoke, there seems to be little exposure to cadmium from passive smoking. No significant effect on blood cadmium concentrations could be detected in children exposed to environmental tobacco smoke.[37]

[edit] Product recalls

[edit] Highbury Seats

In May 2006, a sale of the seats from Arsenal F.C.'s old stadium, Highbury in London, England was cancelled after the seats were discovered to contain trace amounts of cadmium.[38]

[edit] Jewelry

Reports of high levels of cadmium use in children's jewelry in 2010 led to a US Consumer Product Safety Commission investigation. Twelve percent of the 103 items tested from New York, Ohio, Texas and California contained at least 10 percent cadmium, with a single item test claimed to be 91 percent cadmium.[39] The CPSC issued specific recall notices for cadmium content applying to jewelry sold by Claire's[40] and Wal-Mart[41] stores.

[edit] McDonald's drinking glasses

In June 2010 McDonald's voluntarily recalled more than 12 million promotional “Shrek Forever After 3D” Collectable Drinking Glasses due to concerns over cadmium levels in paint pigments used on the glassware.[42] The glasses were manufactured by ARC International, of Millville, NJ.[

 

引用出處: 

 http://en.wikipedia.org/wiki/Cadmium

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铟是银白色并 略带淡蓝色的金属 ,熔点156.61℃,沸点2080℃,密度7.3克/厘米3(20℃)。很软,能用指甲刻痕,比铅的硬度还低。铟的可塑性强,有延展性,可压成极薄的金 属片。从常温到熔点之间,铟与空气中的氧作用缓慢,表面形成极薄的氧化膜,温度更高时,与氧、卤素、硫、硒、碲、磷作用。大块金属铟不与沸水和碱反应,但 粉末状的铟可与水作用,生成氢氧化铟。铟与冷的稀酸作用缓慢,易溶于浓热的无机酸和乙酸、草酸。铟能与许多金属形成合金。铟的氧化态为+1和+3,主要化 合物有In2O3、In(OH)3,与卤素化合时,能形成一卤化物和三卤化物。

纠错 编辑摘要

目录

  • 1 汉字铟
  • 2 词典释义
  • 3 金属铟概述
  • 4 综合性质
  • 5 特性
  •  

  • 1 汉字铟
  • 2 词典释义
  • 3 金属铟概述
    • 3.1 简介
    • 3.2 发现及用途
    • 3.3 存在
    • 3.4 资源
  • 4 综合性质
    • 4.1 物理性质
    • 4.2 化学性质
  • 5 特性
  • 6 发现
  • 7 用途
  • 8 产地
  • 9 危险性
  • 10 提取工艺
  • 11 工业生产中提取铟的方法
  • 12 应用领域
  • 13 中国铟价面临“有市无价”
  • 14 投资前景
  • 15 字源字形

 

铟 - 汉字铟

繁体字:銦

拼音:yīn  

注音:ㄧㄣ

简体部首:钅,部外笔画:6,总笔画:11

繁体部首:金

五笔86&98:QLDY

仓颉:OPWK

郑码:PJD

笔顺编号:31115251341

四角号码:86700

UniCode:CJK 统一汉字 U+94DF铟 繁体字:銦 添至备忘录

拼音:yīn   注音:ㄧㄣ

简体部首:钅,部外笔画:6,总笔画:11

繁体部首:金

五笔86&98:QLDY  仓颉:OPWK  郑码:PJD

笔顺编号:31115251341  四角号码:86700  UniCode:CJK 统一汉字 U+94DF[1]

 

铟 - 词典释义

基本字义

● 铟

(銦)

yīn  ㄧㄣˉ

◎ 一种金属元素,质软,能拉成细丝。可作低熔合金、轴承合金、半导体、电光源等的原料。

详细字义

◎ 铟

銦 yīn

〈名〉

一种软的有延展性的易熔银白色金属元素,原子序数49,不易失去光泽,与铝和镓类似,主要是三价,在闪锌矿和其他矿石中有很小量存在,主要作飞机用的涂敷铅的银轴承的镀层 [indium]——元素符号In

 

铟 - 金属铟概述

简介

铟 (英文:indium),元素符号In,原子序数49,原子量114.82,属周期系ⅢA族。铟是一种柔软的银灰色金属,带有光泽。从常温到熔点之间, 铟与空气中的氧作用缓慢,表面形成极薄的氧化膜,温度更高时,与氧、卤素、硫、硒、碲、磷作用。大块金属铟不与沸水和碱反应,但粉末状的铟可与水作用,生 成氢氧化铟。铟与冷的稀酸作用缓慢,易溶于浓热的无机酸和乙酸、草酸。铟能与许多金属形成合金。铟的氧化态为+1和+3,主要化合物有In2O3、 In(OH)3,与卤素化合时,能形成一卤化物和三卤化物。铟-115是最常见的铟同位素,带有微弱的放射性。

发现及用途

 1863 年F.赖希和H.T.里希特为了寻找铊而研究闪锌矿,用处理矿物所得的硫化物进行光谱分析,发现一条靛蓝色光谱,认为是一种新元素,并命名为 铟,意思是“靛蓝色”,同年分离出金属铟。铟主要作为包复层或与其它金属制成合金,以增强耐腐蚀性;铟有优良的反射性,可用来制造反射镜;铟合金可作反应 堆控制棒;在无线电和半导体技术中,铟及铟的化合物也有重要用途。铟可用作低熔点合金、半导体、整流器、热敏电阻等。含24%铟及76%镓的合金,在室温 下是液体。铟是电子、电信、光电产业不可或缺的关键原材料之一,70%的铟用于制造液晶显示产品,在电子、电信、光电、国防、通讯等领域具有广泛用途,极 具战略地位。铟产业被称为“信息时代的朝阳产业”。

存在

铟在地壳中的含量为 1×10-5%,它虽然也有独立矿物 ,硫铟铜矿(CuInS2)、硫铟铁矿(FeInS4)、水铟矿[In(OH)3],但量极少, 绝大部分铟都分散在其他矿物中,主要是含硫的铅、锌矿物,闪锌矿中铟的含量为0.0001%~0.1%,铅锌冶炼厂和锡冶炼厂都能回收铟。

资源

铟 是非常稀少的金属,全世界铟的地质含量仅为1.6万吨,为黄金地质储量的1/6。铟在地壳中的含量约十万分之一,没有独立矿物,广泛分布于闪锌矿中,含 量在0.1%以下。铟矿物多伴生在有色金属硫化矿物中,特别是硫化锌矿,其次是方铅矿、氧化铅矿、锡矿、硫化铜矿和硫化锑矿等。虽然在一些有色金属精矿中 铟得到初步富集,但由于铟品位低,一般不可直接作为提铟原料。而上述有色金属精矿经过冶炼或高炉炼铁后得到的粗锌、粗铅、炉渣、浸出渣、溶液、烟尘、合 金、阳极泥等是提铟的主要原料。中国拥有世界上最大的铟储量,也是全球最大的铟生产国和出口国,产量占世界铟总产量的30%以上。2006年,中国精铟产 量近6吨,原生铟供应量占全球的60%以上。日本是世界上最大的铟消费国,每年铟需求量占世界铟年产量的70%以上,绝大部分从中国进口。

 

铟 - 综合性质

物理性质

颜色和状态:银白色金属

声音在其中的传播速率(m/S):1215

密度:7.31克/厘米3

熔点:156.61℃

沸点:2080℃

莫氏硬度:1.2

电离能 (kJ /mol) : 5.786电子伏特

M - M+ 558.3

M+ - M2+ 1820.6

M2+ - M3+ 2704

M3+ - M4+ 5200

M4+ - M5+ 7400

M5+ - M6+ 9500

M6+ - M7+ 11700

M7+ - M8+ 13900

M8+ - M9+ 17200

M9+ - M10+ 19700

其它:稀散元素之一,有延展性,比铝软。  

化学性质

元素原子量:114.8

元素类型:金属

原子体积(立方厘米/摩尔):15.7

原子序数:49

元素符号:In

相对原子质量:114.8

核内质子数:49

核外电子数:49

核电荷数:49

氧化态:

主要:In+3

其它:In+1, In+2

质子质量:8.1977E-26

质子相对质量:49.343

所属周期:5

所属族数:IIIA

摩尔质量:115g/mol

外围电子排布:5s2 5p1

核外电子排布:2,8,18,18,3

晶体结构:晶胞为四方晶胞。  

    晶胞参数:

a = 325.23 pm

b = 325.23 pm

c = 494.61 pm

α = 90°

β = 90°

γ = 90°

原子半径:2

其它:易溶于酸或碱;不能分解水;在空气中很稳定;燃烧时会发生鲜紫色的火焰。

 

铟 - 特性

其一:铟金属显银白略带淡蓝色,光泽亮丽,在弯曲时会发出鸣音。其与铜银金的合金制作假牙。熔点156.61°C,沸点2080°C,密度7.3克/厘米³;延展性好,比铅还软。

其 二:铟具有熔点低(156.61°C),沸点高 (2080°C),传导性好,延展性好,比铅还软,能用指甲刻痕;可塑性强,可压成极薄的金属片。其氧化物能形成透明的导电膜等特性,近年在铟锡氧化物 (ITO)、半导体、低熔点合金等方面得到广泛应用。特别是由于铟锡氧化物(ITO)具有可见光透过率95%以上、紫外线吸收率≥70%、对微波衰减率 ≥85%、导电和加工性能良好、膜层既耐磨又耐化学腐蚀等优点,作为透明导电膜已获得广泛应用。随着IT产业的迅猛发展,用于笔记本电脑、电视和手机等各 种新型液晶显示器(LCD)以及接触式屏幕、建筑用玻璃等方面,作为透明电极涂层的ITO靶材(约占铟用量的70%)用量的急剧增长,使铟的需求正以年均 30%以上的增长率递增。世界市场上平面显示器的快速增长成为全世界铟的生产的最主要的最终用户,包括平面电视、台式计算机显示器、可上网的笔记本电脑、 手机等主要的平面显示器的快速发展和应用,使得国际市场对铟的需求急剧增长,而且目前还没有新的用于替代ITO的材料研究出来。

其三、从常 温到熔点之间,铟与空气中的氧作用缓慢,表面形成极薄的氧化膜,温度更高时,与氧、卤素、硫、硒、碲、磷作用。铟在空气中的氧化作用很慢;大块金属铟不与 沸水和碱反应,但粉末状的铟可与水作用,生成氢氧化铟。铟与冷的稀酸作用缓慢,易溶于浓热的无机酸和乙酸、草酸。 铟可作为包复层或与其它金属制成合金,以增强发动机轴承耐腐蚀性;铟有优良的反射性,可用来制造反射镜;银铅铟合金可作高速航空发动机的轴承材料。易熔的 伍德合金中每加1%铟,可降低熔点1.45℃。铟化合物半导体有锑化铟(通迅激光光源、太阳能电池),磷化铟和锑化铟(红外检测、光磁器件、太阳能转换器 等)。 

其四:铟合金可作反应堆控制棒,能够敏感地检测中子幅射;可用于登陆舱,着陆时不脆化、不开裂。 

 

铟 - 发现

1863年,德国的赖希和李希特,用光谱法研究闪锌矿,发现有新元素,即铟。

铊 被发现和取得后,德国弗赖贝格(Freiberg)矿业学院物理学教授赖希由于对铊的一些性质感兴趣,希望得到足够的金属进行实验研究。他在 1863年开始在夫赖堡希曼尔斯夫斯特(Himmelsfüst)出产的锌矿中寻找这种金属。这种矿石所含主要成分是含砷的黄铁矿、闪锌矿、辉铅矿、硅 土、锰、铜和少量的锡、镉等。赖希认为其中还可能含有铊。虽然实验花费了很多时间,他却没有获得期望的元素。但是他得到了一种不知成分的草黄色沉淀物。他 认为是一种新元素的硫化物。

只有利用光谱进行分析来证明这一假设。可是赖希是色盲,只得请求他的助手H.T.李希特进行光谱分析实验。李 希特在第一次实验就成功了,他在分光镜中 发现一条靛蓝色的明线,位置和铯的两条蓝色明亮线不相吻合,就从希腊文中“靛蓝”(indikon)一词命名它为indium(铟)(In)。两位科学家 共同署名发现铟的报告。分离出金属铟的还是他们两人共同完成的。他们首先分离出铟的氯化物和氢氧化物,利用吹管在木炭上还原成金属铟,于1867年在法国 科学院展出。

铟在地壳中的分布量比较小,又很分散。它的富矿还没有发现过,只是在锌和其他一些金属矿中作为杂质存在,因此它被列入稀有金属。

 

铟 - 用途

铟锭因其光渗透性和导电性强,主要用于生产ITO 靶材(用于生产液晶显示器和平板屏幕),这一用途是铟锭的主要消费领域,占全球铟消费量的70%。

其次的几个消费领域分别是:电子半导体领域,占全球消费量的12%;焊料和合金领域占12%;研究行业占6%。另,因为其较软的性质在某些需填充金

属的行业上也用于压缝。如:较高温度下的真空缝隙填充材料。

医学:肝、脾、骨髓扫描用铟胶体。脑、肾扫描用铟-DTPA。肺扫描用铟Fe(OH)**3颗粒。 胎盘扫描用铟Fe抗坏血酸。 肝血池扫描用铟输铁蛋白。

 

铟 - 产地

中国是世界上铟锭主要生产地,此外全球还有美国、加拿大及日本等国生产。

我国的铟分布在铅锌矿床和铜多金属矿床中,保有储量为13014t,分布15 个省区,主要集中在云南(占全国铟总储量的40%)、广西(31.4%)、内蒙古(8.2%)、青海(7.8%)、广东(7%)。

尚未发现铟的单独矿床,它以微量伴生在锌、锡等矿物中。当其含量达十万分之几,就有工业生产价值,目前主要是从闪锌矿中提取。另外,从锌、铅和锡生产的废渣、烟尘中也可回收铟。

 

铟 - 危险性

重金属,有轻微毒性。

健康危害:

铟 比铅还毒。美国和英国已公布了铟的职业接触限值均为0.1 mg/m3[11]。而这两个国家铅的标准为0.15 mg/m3。说明铟的毒性不可轻 视。液晶显示器含有铟,据新华社消息,28岁的黄力(化名)就职于江苏一家生产手机液晶显示屏的企业,主要工作是将一些金属粉喷在液晶屏幕模板上.工作两 年后,他经常呼吸困难、 喘不过气来,检查发现肺部布满雪花状的白色颗粒物.经过半年多时间的医学循征,呼吸科专家认为,黄力是罕见的铟中毒,他血液里的 铟是常规的300倍。黄力肺里的粉尘颗粒无法抽出,所以肺部功能很难恢复,而且还在不断地自我排出蛋白质。所以每隔一个月就要到医院进行一次全肺灌洗,否 则就可能旧病复发,有生命危险。

环境危害: 对环境有危害,对水体可造成污染。

燃爆危险: 可燃,具刺激性。

 

铟 - 提取工艺

 铟的提取工艺以萃取-电解法为主,这也是现今世界上铟生产的主流工艺技术。其原则工艺流程是:含铟原料→富集→化学溶解→净化→萃取→反萃取→锌(铝)置换→海绵铟→电解精炼→精铟。

铟 多数与其性质类似的锌、 铅、铜和锡等共生,现已发现有自然铟、硫铟铁矿(FeIn2S4)、硫铟铜矿(CuInS2)、硫铜锌铟矿[(Cu,Zn,Fe)3(In,Sn)S4] 和羟铟矿[In(OH)3]等5种含铟矿物。铟在硫化矿中的含量最高,闪锌矿是主要工业来源,铜矿、方铅矿、黄锡矿与锡石也含有较高的铟,但由于产量极 少,非常分散,不能作为直接生产铟的原料,一般是从锌、铅、锡等重金属冶炼的副产物中回收生产。由于稀散金属离子在化学性质上有许多相似之处,造成分离、 富集、回收上的困难,近年来,随着铟需求量不断增加,对于铟的富集、回收进行了很多的研究。

世界上铟产量的90% 来自铅锌冶炼厂的副产 物。铟的冶炼回收方法主要是从铜、 铅、锌的冶炼浮渣、熔渣及阳极泥中通过富集加以回收。根据回收原料的来源及含铟量的差别,应用不同的提取工艺,达到最佳配置和最大收益。常用的工艺技术有 氧化造渣、金属置换、电解富集、酸浸萃取、萃取电解、离子交换、电解精炼等。当前较为广泛应用的是溶剂萃取法,它是一种高效分离提取工艺。离子交换法用于 铟的回收,还未见工业化的报导。在从较难挥发的锡和铜内分离铟的过程中,铟多数集中在烟道灰和浮渣内。在挥发性的锌和镉中分离时,铟则富集于炉渣及滤渣 内。

 

在ISP炼铅锌工艺中,精矿中的铟较大部分富集于粗锌精馏工序产出的粗铅中,回收富铟粗铅的铟,一直采用碱煮提铟工艺,存在生产能力小、生产成本高、金属回收率低等缺点。

为 了简化铟的提取流程,降低生产成本,提高金属回收率,针对原有的提铟生产工艺,本项目通过条件试验、循环实验及综合试验,研究开发了“富铟粗铅电 解-铅电解液萃铟”提取工艺,确定了新工艺的最佳工艺参数。工艺流程为:粗铅熔化铸成极板,装入电解槽通电进行电解,阳极中的铟溶解进入电解液,当铟富集 到一定浓度后,抽出电解液进行萃取、反萃,富铟反萃液经pH调节、置换、压团熔铸后得到粗铟。[2]

 

铟 - 工业生产中提取铟的方法

 

1、从炼锌副产品中回收铟

日 本同和矿业公司以炼锌中产生的净液残渣作为原料,先分离和浸出,脱铜、脱铝,除去原料中与镓铟性质相似的重金 属,然后在富集镓铟的溶液中加入盐酸,混合搅拌,调整酸度之后,再用醚萃取铟,使它和镓及其它金属分离。最后用水反萃出铟,再经置换,熔融和电解。 在每 次电解中需调整电流密度和电解液的酸度,以除去微量的镉、 锡和铝等,生产出4 N 以上的金属铟。此外,铟的选择性分离法是把铅、锌冶炼过程中产生的含有微量的铟烟尘、阳极泥等各种残渣以及电解排出液作为原料, 采用含萃取剂膦酸二(2-乙基己基)酯的有机溶剂,于pH小于1.0的条件下,对含铟及其它金属的硫酸溶液萃取,然后用盐酸在30-700C 进行反萃, 从而选择性分离铟。其萃取铟的效率可高达98%以上。

 

2、硬锌真空蒸馏提锌和富集锗铟银

“硬锌真空蒸馏提 锌和富集锗铟银”项目属于材料学科,冶金技术领域科研项目。硬锌是粗锌火法精馏过程中 产出的一种中间产物,是由粗锌中的高沸点物质组成,其主要是以锌铅铁砷为主体并含有锗铟银等元素的多元合金。硬锌的产出率约占粗锌处理量的4%。由昆明理 工大学中国工程院院士戴永年等人主持研究的“硬锌真空蒸馏提锌和富集锗铟银”项目获得了2003年度国家技术发明奖二等奖。

该技术用“真 空蒸馏法提锌和富集锗铟银”的新流程及新工艺,并成功地研制了与该工艺流程配套的生产设备,突破了常规的在现有生产技术上进行技术改造 的传统做法,取得了成功。有关专家评价道,该发明工艺属国内首创,且安全可靠,操作方便,无“三废”污染,属“绿色冶金”新技术,符合国家所倡导的资源综 合利用的可持续发展战略,具有新颖性、创造性和实用性。

 

3、从矿渣中回收金属铟

从锑、锌矿渣中回收金属铟 一般采用酸化浸出-萃取法。在其他矿渣中如铁矾渣、铜渣等也含有稀散金属铟。冰铜冶炼转炉吹炼得到的铜渣中铟含量达0.6%~0.95%,具有较大的回收 价值。从铁矾渣中富集、回收铟可采用还原挥发处理和萃取提铟新工艺,将铁矾渣在高温下用炭还原,并加入某助剂使铟从渣中挥发出来,形成富铟物料,再进行浸 出-萃取-电积,可得到纯度为99.99%的高纯铟,铟回收率大于80% ,同时解决了铁矾渣的污染问题。

 

4、从烟灰中回收金属铟

冶 炼烟灰中主要含有锌、铅、铜和铁等金属,同时含有少量铟。铟在冶炼烟灰中主要以In2O3,In2S3和 In2(SO4)3等物相存在。从冶炼烟灰中回收铟主要采用酸浸—溶剂萃取法。株洲冶炼集团采用硫酸直接浸出—萃取法从铅浮渣反射炉烟尘中提取铟,在 200g?L-1硫酸溶液中浸出,铟的浸出率为90%,用P204作萃取剂,适当条件下溶液中铟的萃取率可达85%,用HCl作反萃剂,反萃率在95%以 上。在酸浸过程中加入NaCl有利于进一步提高铟的浸出率。对铅烟灰进行酸化焙烧—水浸,铟浸出率提高到88%以上。在萃取过程中采用P204水平箱萃取 法,铟的萃取率从90%提高到95%。

 

5、从废水中回收金属铟

1)萃取法

在铟的富集与回收中,萃取是重要的方法,萃取剂包括二(2一乙基己基)膦酸(HDEHP、P204),P5708、P507D、P350、PV?HQPF、Cyanex923、TR-PO、TBP和石油亚砜等。

 

2)离子交换法

萃淋树脂具有萃取剂流量少,柱负载量高,传质性能好等优点,广泛应用于分离工程。

 

3)液膜法

液膜分离法是一种高效、快速、节能的高新分离技术。以P291为流动载体,L113A为表面活性剂,液体石腊为膜增强剂,煤油为膜溶剂,硫酸和硫酸肼水溶液为内相试剂,用该乳状液膜体系对铟进行分离富集。

 

6、从合金中回收金属铟

以 铅、锡等为主体的多元合金及金属化合物,含有铟、锗等有价金属,可采用碱熔、酸浸的方法回收铟、锗等有价金属。 如电炉底铅是以铅、锡等为主体的多元合金及金属化合物,往电炉底铅中加入NaOH,进行碱熔和碱煮,将细浸出渣酸浸,两段酸浸的铟总浸出率达99%,铟直 收率达84.3%。

中国铟的提取工艺在上世纪90年代初获得突破,在有色金属工业快速发展的大背景下,铟的提取工艺普及非常快,特别是铟 价高涨之后,铟的综合回收受到 企业的普遍重视,国内科研单位和生产企业针对各种含铟物料的提铟工艺又取得长足进展,因此中国铟产量增长迅速。主要生产厂家工艺特点在于针对不同的含铟原 料采取不同的初步富集方法和溶解技术,再根据介质情况选择适合的萃取剂。如华锡集团和柳州铟泰科技有限责任公司提铟原料为含铟量大约0.2%的炼锌铁钒 渣;葫芦岛锌厂、韶关华力公司、韶关冶炼厂则是从含铟2%~3%的硬锌块中提铟;株洲冶炼厂用置换渣(铟2%~3%)作为提铟原料;柳州锌品公司从生产立 德粉的浸出渣(含铟0.2%)中提炼。[3]

 

铟 - 应用领域

铟 称得上“合金的维生素”,铟合金可用作钎焊料,铟是无铅焊料新的重要添加元素,世界无铅焊料的发展趋势有利于铟钎焊料的应用。利用铟合金熔点低的 特点还可制成特殊合金,用于消防系统的断路保护装置及自动控制系统的热控装置;添加少量铟制造的轴承合金是一般轴承合金使用寿命的4-5倍;铟合金还可用 于牙科医疗、钢铁和有色金属的防腐装饰件、塑料金属化等方面。

由于铟具有较强的抗腐蚀性及对光的反射能力,可制成军舰或客轮上的反射镜。铟对中子辐射敏感,可用作原子能工业的监控剂量材料,目前用在原子能工业的铟,大约与电子工业上的用量相近。

铟 可在蓄电池中作添加剂,在无汞碱性电池中作为缓蚀剂,可使电池成为绿色环保产品。铟在防止雾化层方面的用量不断增加,铟涂层最初是在汽车制造业中 采用,有可能普及到工业及高档民用建筑业中去。日本索尼公司发明了以铟代替钪的新阴极,这样每根电子枪的成本就降到了掺钪电子枪的十分之一左右。因此,在 电视机大功率输出、长寿命方面,铟的应用发展前景引人注目。

在光电子领域,铟及其化合物半导体具有广泛的用途。在铟基III-V族化合物 半导体如锑化铟(INSB)、磷化铟(INP)、砷化铟(INAS)等 中,研究和应用最早的是锑化铟(INSB),而最受重视并具有潜在应用前景的是磷化铟(INP),它在微波通讯向毫米波通讯方面,作为光纤通讯的激光光源 和异质结太阳能电池材料方面,都有突破性进展,展现了铟应用的可喜前景。锑化铟和砷化铟在红外探测和光磁器件方面也有重要用途。在太阳能电池中,含铟化合 物薄膜材料正异军突起,以其高转换率、低成本、便于携带等优势受到瞩目。

铜铟硒(CIS)等I-II-VI三元化合物薄膜半导体材料,由于 有价格低廉、性能良好和工艺简单的优点,将成为今后大力发展太阳电池工业的一个重 要方向,促使铟在该领域的应用不断增大。以信息技术为中心的新产业已经兴起,铟锡氧化物(ITO)是各类平板显示器不可缺少的关键材料,目前全世界的铟有 75%左右消耗在这方面,未来仍然大有作为。不仅如此,随着铟的提取、加工技术不断进步,生产成本的降低,铟的应用还在继续拓展。 [4]

 

铟 - 中国铟价面临“有市无价”

 

中国铟资源丧失定价权 日本加工后10倍价钱买回 

在经历了年初短暂的行业回暖后,目前的铟价正面临“有市无价”的尴尬。“近期铟价显现出疲弱迹象,需求也不旺,预计报价还将有小幅下滑。”天津稀有金属交易中心信息中心工作人员王先生对 《每日经济新闻》表示。

目 前铟价为现货商询价2778元~3000元/千克 (不含税),市场价格则为3100元/千克。而在今年8月份,铟价还维持在3600元/千克,短短几个 月间整整下降了500元。事实上,产量仅为银的1%的铟一直被外界看好。按照产业分析人士的估值,铟的合理价值应在2000~3000美元/千克,也就是 目前铟价的大约6倍。稀缺战略资源因何遭遇价格“尴尬”?《每日经济新闻》对此进行了调查。

19家企业联合争夺定价权

相 关资料显示,中国是全球第一大原生铟供应国,然而,这一垄断性资源优势却没有体现出 “中国价值”,铟资源价格长期遭受外国厂家的压制。19家中国具有 铟出口资质和配额的企业就MB(MetalBul-letin,英国《金属导报》周刊)的精铟报价问题发表联合声明:认为MB报道的精铟价格不能代表当前 中国市场的主流价格;2010年6月中旬以来,中国厂商未曾以MB所报道的低价出货,上述企业要求MB公正地发布即时市场价格,否则将联合业内人士拒绝参 照MB的报价,并拒绝向其提供任何有关信息。

 

19家企业“激烈”行动背后正是中国在国际铟市场缺少话语权的具体体现。据 《每日经济新闻》了解,自6月9日以来。MB对铟金属的最低报价就一直维持在 520美元/千克,中国企业对此明确提出异议,认为MB报价低于市场主流价格;MB声称其报道的低价确为中国出口的不含税价格。在几次与MB沟通未果的情 况下,中国企业通过公开申明的方式表明自己的立场。而中国有色金属工业协会铟业分会(以下简称铟业分会)也表态称,中国是铟最主要的原产地,理应在铟的价 格问题上更有话语权。“从6~7月份,铟业分会就MB低报中国铟价格与对方进行了一个半月的艰难磋商,最后迫使MB正视中国企业的要求,提高了报价。”铟 业分会会长赵立奎表示。 

 

约九成小铟厂退出市场 

铟矿多伴生在有色 金属硫化矿物中,特别是硫化锌矿,其次是方铅矿、氧化铅矿、锡矿等,需通过相关工艺才能提炼出铟,目前包括株冶集团、中金岭南、ST锌 业、ST珠峰、罗平锌电等企业都有铟业务。方正证券铟业分析师邓新荣表示,对于株冶集团等企业来说,铟并不是主营业务,而是副产品,生产成本低,因此价格 也往往不高,这也造成了铟价格一直被市场低估。

 

作为中国最重要的有色金属冶炼基地之一,云南省已探明的铟储量占到了全国的40%左右。以个旧地区为例,当地铟资源富集于铅、锡、锌、铜等矿中,原先精加工铟厂有乘风有色金属、云锡集团、自立矿冶厂等企业,另有十余家粗加工铟厂。

 

由于国内在产业链延伸方面的科技投入不够,致使铟的深加工产品不能生产,国内下游行业直接消费少,精铟必须依赖出口。但是来自欧美及铟主要消费国日本的厂家需求持续低迷,加上走私现象猖獗,出口市场只能不断以低价进行竞争。

 

与铟价的低迷相比,各种提取铟的原材料价格却在不断上涨,另外,环保等方面的要求日益严格,许多小铟厂被迫关闭。“整体关闭了90%,现在只剩下2家了.

 

个旧市双龙贵金属实业有限公司高经理在接受记者采访时表示,目前提炼铟的各种辅助材料价格一直上涨,挤压了粗铟的利润空间。由于没有成熟的处理铟生产废水的方法,这些企业承受着巨大的环保压力。“国家实行节能减排之后,光环保一项就让铟厂的成本增加了20%。”

 

压 力不止于此,2007年6月18日开始,中国对铟出口实行许可证和配额管理,并征收15%的关税。而在此前,出口铟可以享受退税13%。一进一退之间利 润的巨大下滑也让林炼焕下定决心关闭了小铟厂,转行做铜业生意了。在个旧颇有实力的乘风有色金属也停止了铟业生产,据公司段总经理介绍,由于没有利润,厂 里虽然拥有铟出口配额,但也不得不停止生产。

 

根据铟业分会的统计,从2007年开始,中国精铟产量连续3年逐年下降。为此,国家在政策上又进行了一番调整,从2009年7月1日起,对“未锻轧铟、废碎料”的出口暂定关税由原先的15%下调为5%,“铟粉末”出口暂定关税由10%下调为5%。 

 

日本控制铟加工核心技术 

虽然中小铟厂退出市场、关税提高等因素让铟出口下降,但这丝毫没有阻止外资染指中国铟资源的热情。在《每日经济新闻》的调查中发现,这些外资正以更为隐蔽的方式来获取中国的铟资源,其中以日本最为典型。 

 

日本是铟需求大国,中国70%的铟出口日本。但是日本将这些原产铟加工成高端产品后,又高价卖给中国企业。

 

中国国内铟产业的发展存在“群龙无首”、中小企业当道的现象,目前拥有100多家铟厂,铟资源呈分散状态,约95%的生产厂家年生产量仅在1~5吨,且多数只能加工初级原料产品。 

 

作 为最大的铟采购商,日本企业主要采取的是分散采购的方式。日本企业最常用的做法是到铟厂比较集中的区域挨个打听铟厂的产能,然后“狮子大开口”,要求采 购。比如你的产能只有1吨,那么他就会开口说要3吨,因为产能达不到,再加上是国际贸易,所以小铟厂往往不敢贸然接单。实际上,各家铟厂的情况基本已被日 本买家摸透,然后这些日本买家就开始动用国内招聘的中间采购商几百斤几百斤地从这些小铟厂购买,以达到压价的目的。

 

日商从大量公开采购转为小量分散采购,一方面是在采购战略性极强的物资上避开国际市场的关注,另一方面巧妙利用采购时间差,扭曲正常的供求关系,并配合以舆论宣传、恶意打压来操纵市场价格,坐收渔利。 

 

中小铟厂规模小,许多企业因资金缺乏,迫于生存的压力只能竞相压价出货,从而造成了长期以来极具战略储备意义的铟资源大量低价流失。

 

更为严重的是,在铟产业链中,中国通过消耗大量的铟资源赚取微薄的利润,而日本等国却将每年从中国大量进口的低价铟加工成高端产品,再以高价卖给中国。铟靶材(ITO粉)就是其中之一。

 

铟 是ITO靶材生产的主要原料,自1994年以来,中国国内有不少企业联合高校对相关技术进行研发,但至今无法掌握高品质ITO靶材制作所需之技术,这些 技术目前主要被日本的几大公司掌握,日本矿业公司、三井产业等4家企业控制着全世界95%左右的ITO靶材市场份额。此前有媒体报道称,株冶集团等国内公 司曾与日本企业进行过谈判,但一直无法引进相关技术。

 

以目前的市场价格为例,中国出口精铟价格仅为每吨300万元左右,但从日本进口的铟靶材(ITO粉)高达每吨两三千万元,价格接近精铟的10倍,利润可见一般。[6]

 

铟 - 投资前景

铟在世界属于稀缺资源。全球预估铟储量仅5万吨,其中可开采的占50%。由于目前未发现独立铟矿,工业通过提纯废锌、废锡的方法生产金属铟,回收率约为50-60%,这样,真正能得到的铟只有1.5-1.6万吨。

基于铟的稀缺和不可替代性,美国从1985年开始金属铟的储备。2007年,日本也将铟列入战略储备金属名单。中国拥有世界上80%的铟储量,却没有铟的定价权,走私情况猖獗,走私量甚至大于正常出口量。中国对铟资源的保护还有待加强。

上世纪二三十年代,铟首先应用于合金材料的生产。八十年代,铟被大量用于电子工业。至06年,铟的用量逾千吨,广泛用于发光材料、半导体轴承制造。铟作为一种优良的改性剂,有“金属维他命”之称。良好的商品属性支撑了铟的金融属性的开发。

铟具有很好的保值性能。当前,一些金融部门、南方的投行已经接受铟作为融资工具进行抵押贷款。

铟 还可以作为投机工具活跃于资本市场。一般金属行情波动周期为5-7年,而铟则相对的具有很好的价格波动性。每年铟价会有两轮涨势。由于日本是目前 最大的铟消费国,每年4月份日本的通关优惠政策会导致日本采购大增,铟价暴涨。而11月底前日韩企业则会为第二年生产提前2-3月大量采购,价格也会小 涨。从2001年1月至今,铟价涨跌可为跌宕起伏,最低时只有50美元/千克,最高达到1050美元/千克。如此波动的行情有利于投机者利用金融杠杆进行 有效操作,获取大量利益。

未来,铟还可能与股票债券等硬性资产相提并论,用作风险规避。铟与银价值非常相近,而相比之下铟更加稀缺。铟优 于黄金投 资的理由还在于,金价已经到达一个高位,绝无翻倍可能(全球黄金储量以16万吨计,接盘需要79万亿美元,这显然是不可能的),而铟的储量则只有1.5万 吨,用量却以每年20-30%的比率上升,未来价格有翻倍可能,甚至会回到1000美元的高位。尽管短期内市场暂时疲软,但长期来看,如果没有强力的替代 材料出现,铟的价格总会有所突破。

 

引用出處: 

 http://www.hudong.com/wiki/%E9%93%9F

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Indium ( /ˈɪndiəm/ IN-dee-əm) is a chemical element with chemical symbol In and atomic number 49. This rare, very soft, malleable and easily fusible post-transition metal is chemically similar to aluminium. Indium was discovered in 1863 and named for the indigo blue line in its spectrum that was the first indication of its existence in zinc ores, as a new and unknown element. The metal was first isolated in the following year. Zinc ores continue to be the primary source of indium, where it is found in compound form. Very rarely the element can be found as grains of native (free) metal, but these are not of commercial importance.

Indium's current primary application is to form transparent electrodes from indium tin oxide in liquid crystal displays and touchscreens, and this use largely determines its global mining production. It is widely used in thin-films to form lubricated layers (during World War II it was widely used to coat bearings in high-performance aircraft). It is also used for making particularly low melting point alloys, and is a component in some lead-free solders.

Indium is not known to be used by any organism. In a similar way to aluminum salts, indium (III) ions can be toxic to the kidney when given by injection, but oral indium compounds do not have the chronic toxicity of salts of heavy metals, probably due to poor absorption in basic conditions. Radioactive indium-111 (in very small amounts on a chemical basis) is used in nuclear medicine tests, as a radiotracer to follow the movement of labeled proteins and white blood cells in the body.

 

 

Contents

[hide]

  • 1 Characteristics
  • 2 Isotopes
  • 3 Creation
  • 4 History
  • 5 Occurrence and consumption
    • 5.1 Resources
    • 5.2 Production
  • 6 Applications
    • 6.1 Electronics
    • 6.2 Metal and alloys
    • 6.3 Other uses
  • 7 Precautions
  • 8 See also
  • 9 References
  • 10 External links

[edit] Characteristics

 

 

 

 

Indium wetting the glass surface of a test tube

Indium is a very soft, silvery-white, relatively rare true metal with a bright luster. As a pure metal, indium emits a high-pitched "cry", when it is bent.[2] Both gallium and indium are able to wet glass. A number of standard electrode potentials, depending on the reaction under study,[3] is reported for indium:

- 0.40 In2+ + e− ↔ In+

 

 

- 0.49 In3+ + e− ↔ In2+

 

 

- 0.40 In2+ + 3 e− ↔ In+

 

 

- 0.338 In3+ + 3 e− ↔ Ino

Unlike its period 5 neighbor cadmium, indium is not a cumulative poison.

Indium demonstrates the inert pair effect to a limited extent, forming some In (I) compounds such as Indium(I) bromide. The most stable oxidation state for indium, however, is still (III). Unlike the corresponding thallium compounds, indium (I) compounds are not stable in water.

[edit] Isotopes

Main article: Isotopes of indium

Indium in nature consists of two primordial nuclides. One unusual property of indium (shared only with rhenium) is that although it possesses a stable isotope, its most common (abundant) isotope (95.7%) is slightly and measurably radioactive. This isotope, indium-115 very slowly decays by beta emission to tin. This decay has a half-life of 4.41×1014 years, four orders of magnitude larger than the age of the universe and nearly 50,000 times longer than that of natural thorium.[4]

[edit] Creation

Indium is created via the long S-process in low-medium mass stars (.6 -> 10 solar masses). This takes thousands of years to do. It requires a cadmium atom to capture sufficient neutrons and then undergo Beta decay.

[edit] History

In 1863 the German chemists Ferdinand Reich and Hieronymous Theodor Richter were testing ores from the mines around Freiberg, Saxony. They dissolved the minerals pyrite, arsenopyrite, galena and sphalerite in hydrochloric acid and distilled the raw zinc chloride. As it was known that ores from that region sometimes contain thallium they searched for the green emission lines with spectroscopic methods. The green lines were absent but a blue line was present in the spectrum. As no element was known with a bright blue emission they concluded that a new element was present in the minerals. They named the element with the blue spectral line indium, from the indigo color seen in its spectrum.[5][6] Richter went on to isolate the metal in 1864.[7] At the World Fair 1867 an ingot of 0.5 kg (1.1 lb) was presented.[8]

[edit] Occurrence and consumption

Indium ranks 61st in abundance in the Earth's crust at approximately 0.25 ppm,[9] which means it is more than three times as abundant as silver, which occurs at 0.075 ppm.[10] Fewer than 10 indium minerals are known, none occurring in significant deposits. Examples are the dzhalindite (In(OH)3) and indite (FeIn2S4).[11]

[edit] Resources

Based on content of indium in zinc ore stocks, there is a worldwide reserve base of approximately 6,000 tonnes of economically viable indium.[12] This figure has led to estimates suggesting that, at current consumption rates, there is only 13 years' supply of indium left.[13] However, the Indium Corporation, the largest processor of indium, claims that, on the basis of increasing recovery yields during extraction, recovery from a wider range of base metals (including tin, copper and other polymetallic deposits) and new mining investments, the long-term supply of indium is sustainable, reliable and sufficient to meet increasing future demands.[14]

This conclusion also seems reasonable in light of the fact that silver, three times less abundant than indium in the earths crust,[15] is currently mined at approximately 18,300 tonnes per annum,[16] which is 40 times greater than current indium mining rates.

[edit] Production

The lack of indium mineral deposits and the fact that indium is enriched in sulfidic lead, tin, copper, iron and predominately in zinc deposits, makes zinc production the main source for indium. The indium is leached from slag and dust of zinc production. Further purification is done by electrolysis.[8]

Indium is produced mainly from residues generated during zinc ore processing but is also found in iron, lead, and copper ores.[2] Canada is a leading producer of indium. The Teck Cominco refinery in Trail, British Columbia, is the largest single source indium producer, with production of 32,500 kg in 2005, 41,800 kg in 2004 and 36,100 kg in 2003. South American Silver's Malku Khota property in Bolivia is the largest resource of indium with an indicated resource of 845,000 kg and inferred resource of 968,000 kg.Adex Mining Inc.’s Mount Pleasant Mine in New Brunswick, Canada, holds about 15 to 20% of the world’s total known indium resources.[17]

The amount of indium consumed is largely a function of worldwide LCD production. Worldwide production is currently 476 tonnes per year from mining and a further 650 tonnes per year from recycling.[14] Demand has risen rapidly in recent years with the popularity of LCD computer monitors and television sets, which now account for 50% of indium consumption.[18] Increased manufacturing efficiency and recycling (especially in Japan) maintain a balance between demand and supply. Demand increased as the metal is used in LCDs and televisions, and supply decreased when a number of Chinese mining concerns stopped extracting indium from their zinc tailings. In 2002, the price was US$94 per kilogram. The recent changes in demand and supply have resulted in high and fluctuating prices of indium, which from 2005 to 2007 ranged from US$700/kg to US$1,000/kg.[12] Demand for indium may increase with large-scale manufacture of CIGS-based thin film solar technology starting by several companies in 2008, including Nanosolar and Miasole.

[edit] Applications

 

 

 

 

A magnified image of an LCD screen showing RGB pixels. Individual transistors are seen as white dots in the bottom part.

The first large-scale application for indium was as a coating for bearings in high-performance aircraft engines during World War II. Afterward, production gradually increased as new uses were found in fusible alloys, solders, and electronics. In the 1950s, tiny beads of it were used for the emitters and collectors of PNP alloy junction transistors. In the middle and late 1980s, the development of indium phosphide semiconductors and indium tin oxide thin films for liquid crystal displays (LCD) aroused much interest. By 1992, the thin-film application had become the largest end use.[19][20]

[edit] Electronics

  • Indium oxide (In2O3) and indium tin oxide (ITO) are used as a transparent conductive coating applied to glass substrates in the making of electroluminescent panels.
  • Some indium compounds such as indium antimonide, indium phosphide,[21] and indium nitride[22] are semiconductors with useful properties.
  • Indium is used in the synthesis of the semiconductor copper indium gallium selenide (CIGS), which is used for the manufacture of thin film solar cells.[23]
  • Used in light-emitting diodes (LEDs) and laser diodes based on compound semiconductors such as InGaN, InGaP that are fabricated by Metalorganic Vapor Phase Epitaxy (MOVPE) technology.
  • The ultrapure metalorganics of indium, specifically high purity trimethylindium (TMI) is used as a precursor in III-V compound semiconductors, while it is also used as the semiconductor dopant in II-VI compound semiconductors.[24]
  • As one of many substitutes for mercury in alkaline batteries to prevent the zinc from corroding and releasing hydrogen gas (e.g., US Pat US5188869)

[edit] Metal and alloys

 

 

 

 

Ductile indium wire

  • Very small amounts used in aluminium alloy sacrificial anodes (for salt water applications) to prevent passivation of the aluminium.
  • To bond gold electrical test leads to superconductors, indium is used as a conducting glue and applied under a microscope with precision tweezers.
  • In the form of a wire it is used as a vacuum seal and a thermal conductor in cryogenics and ultra-high vacuum applications. For example, in manufacturing gaskets which deform to fill gaps.[25]
  • Used as a calibration material for Differential scanning calorimetry.
  • It is an ingredient in the alloy Galinstan, which is liquid at room temperature while not being toxic like mercury.

[edit] Other uses

  • Indium tin oxide is used as a light filter in low pressure sodium vapor lamps. The infrared radiation is reflected back into the lamp, which increases the temperature within the tube and therefore improves the performance of the lamp.[20]
  • Indium's melting point of 429.7485 K (156.5985 °C) is a defining fixed point on the international temperature scale ITS-90.
  • Indium's high neutron capture cross section for thermal neutrons makes it suitable for use in control rods for nuclear reactors, typically in an alloy containing 80% silver, 15% indium, and 5% cadmium.
  • In nuclear engineering, the (n,n') reactions of 113In and 115In are used to determine magnitudes of neutron fluxes.
  • Indium is also used as a thermal interface material by personal computer enthusiasts in the form of pre-shaped foil sheets fitted between the heat-transfer surface of a microprocessor and its heat sink. The application of heat partially melts the foil and allows the indium metal to fill in any microscopic gaps and pits between the two surfaces, removing any insulating air pockets that would otherwise compromise heat transfer efficiency.
  • 111In emits gamma radiation and is used in indium leukocyte imaging, or indium scintigraphy, a technique of medical imaging. Indium leukocyte scintigraphy has many applications, including early phase drug development, and the monitoring of activity of white blood cells. For the test, blood is taken from the patient, white cells removed, labeled with the radioactive 111In, then re-injected back into the patient. Gamma imaging will then reveal any areas of on-going white cell localization such as new and developing areas of infection.

[edit] Precautions

Pure indium in metal form is considered non-toxic by most sources. In the welding and semiconductor industries, where indium exposure is relatively high, there have been no reports of any toxic side-effects.

Indium compounds, like aluminum compounds, complex with hydroxyls to form insoluble salts in basic conditions, and are thus not well-absorbed from food, giving them fairly low oral toxicty. Soluble indium (III) is toxic when delivered parenterally, however, causing damage primarily to the kidney (both inner and outer parts). Other indium compounds are toxic when administered outside the GI tract: for example, anhydrous indium trichloride (InCl3) and indium phosphide (InP) are quite toxic when delivered into the lungs (the latter is a suspected carcinogen).[

 

引用出處: 

 http://en.wikipedia.org/wiki/Indium

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镓是银白色金 属。密度5.904克/厘米3。熔点29.78℃。沸点2403℃。化合价2和3。第一电离能5.999电子伏特。凝固点很低。由于稳定固体的复杂结构, 纯液体有显著的过冷的趋势,可以放在冰浴内几天不结晶。质软、性脆,在空气中表现稳定。加热可溶于酸和碱;与沸水反应剧烈,但在室温时仅与水略有反应。高 温时能与大多数金属作用。由液态转化为固态时,膨胀率为3.1%,宜存放于塑料容器中。

纠错 编辑摘要

目录

  • 1 概述
  • 2 理化性质
  • 3 综合性质
  • 4 发现
  • 5 来源及用途
  •  

  • 1 概述
  • 2 理化性质
  • 3 综合性质
  • 4 发现
  • 5 来源及用途
  • 6 高纯镓
  • 7 硝酸镓
  • 8 磷酸镓
  • 9 氧化镓
  • 10 提炼
  • 11 参考资料

 

高纯镓

 

 

镓 - 概述

镓 是元素周期表第四周期ⅢA族元素,元素符号Ga,原子序数31,原子量69.723。1875年法国化学家布瓦博德朗在闪锌矿中离析出几克性质与门捷列夫 预言的“类铝”相同的元素,并命名。元素名来源于他的祖国,愿意为“法国的”。镓是化学史上第一个先从理论预言,后在自然界中被发现验证的化学元素。镓在 地壳中的含量约0.001%,含量最富的锗石中也只含0.5%左右。固体镓为蓝灰色,液体镓为银白色;熔点29.78°C,沸点2403°C,固体密度 5.907克/厘米³。镓与钒、铌、锆形成的合金具有超导性。

 

镓 - 理化性质

 

金 属镓固态为淡蓝色,液态呈银白色,熔点29.93`C,沸点2403`C,密度5.9g电阻率27x10-8fI•m,液态镓的蒸气压很 低,1350℃时仅为133.3Pa,在所有元素中,镓的液态温度范围最宽(从29.93-2403'C),由于固态镓的结构复杂,液态镓易出现过冷现 象,在快速冷却时,液体镓可以在一40℃的过冷状态下仍保持液态。液态镓转为固态时,镓体积膨胀,膨胀率达3.2%,液态镓几乎能润湿所有物质的表面,具 有优良的浇注性能,镓能迅速扩散到某些金属的晶格内,在高温下能和许多金属生成合金。

镓的外电子层构型为「Ar]3d104s2p1, 有+1--+3三种价态,其中以+3价化合物最稳定。镓在常温空气中稳定,260℃时才开始和氧作 用,100℃时钵不和水作用,但200℃时高压水蒸气会氧化镓生成氢氧化镓。镓的化学性质和锌、铝相似,属于两性元素。和铝相似,既能溶于酸,又能溶于 碱。镓的化学活性和锌相近,但不如铝活泼。镓缓慢溶于硫酸和盐酸中,室温下不溶于硝酸,但溶于热的硝酸、高氯酸、氢氟酸和王水中。随纯度提高,镓在酸和碱 中溶解速度变慢,镓能和卤素作用生成各种卤化物,和硫、硒、磷、砷、锑生成半导体性质的化合物,金属镓腐蚀很强,镓对人体无害,是一种安全金属。

 

镓 - 综合性质

 

元素名称:镓

元素原子量:69.72

元素类型:金属

原子体积:(立方厘米/摩尔):11.8

高纯三甲基镓

 

地壳中含量:(ppm):18

元素在太阳中的含量:(ppm):0.04

元素在海水中的含量:(ppm):  0.00001

 

发现人:布瓦博德朗    发现年代:1875年

原子序数:31

元素符号:Ga

元素英文名称:Gallium

相对原子质量:69.72

核内质子数:31

核外电子数:31

核电核数:31

质子质量:5.1863E-26

质子相对质量:31.217

所属周期:4

所属族数:IIIA

摩尔质量:70

氢化物:GaH3

氧化物:Ga2O3

最高价氧化物化学式:Ga2O3

密度:5.907

熔点:29.78

沸点:2403.0

以下为增加内容:

氧化态:Main  Ga+3

Other  Ga+1, Ga+2

声音在其中的传播速率:(m/S):2740

 

晶胞参数:

a = 451.97 pm

b = 766.33 pm

c = 452.6 pm

α = 90°

β = 90°

γ = 90°

 

电离能 (kJ/ mol) 

M - M+ 578.8

M+ - M2+ 1979

M2+ - M3+ 2963

M3+ - M4+ 6200

M4+ - M5+ 8700

M5+ - M6+ 11400

M6+ - M7+ 14400

M7+ - M8+ 17700

M8+ - M9+ 22300

M9+ - M10+ 26100

 

外围电子排布:4s2 4p1

晶体结构:晶胞为正交晶胞。

莫氏硬度:1.5 

核外电子排布:2,8,18,3

颜色和状态:蓝白色金属

原子半径:1.81

常见化合价:+3

 

镓 - 发现

在化学元素周期系建立的过程中,性质相似的元素成为一族已为化学家们接受。当时法国化学家布瓦邦德朗利用光谱分析发觉到,在铝族中,在铝和铟之间缺少一个元

金属镓,镓锭

素。 从1865年开始,他用分光镜寻找这个元素, 分析了许多矿物,但是都没有成功。直到1875年9月,布瓦邦德朗在法国化学家们面前表演了一组实验,证明新元素的存在。当时布瓦邦德朗测定的新元素比重 是4.7,而门捷列夫根据元素周期系推算出的比重应该是5.9~6。布瓦邦德朗又重新测定了这种新元素,证实了比重应该是5.96。他将此物质命名为 gallium,元素符号定为Ga。

镓的发现不仅是一个化学元素的发现,它的发现引起了科学家们对门捷列夫制定的元素周期系的重视,使化学元素周期系得到赞扬和承认。发现人:布瓦博德朗,发现时间和地点:1875在法国的布瓦博德朗在用光谱分析从闪锌矿得到的提取物时,发现了镓。。

 

镓 - 来源及用途

 

元素来源:它凝固时膨胀,,常是作为从铝土矿中提取铝或从锌矿石中提取锌时的副产物得到的。

元 素用途:用于半导体工业,发光二极管和 砷化镓激光二极管。其他化合物:GaCl3-氯化锌,一种稀有蓝白色三价金属元素,在低温时硬而脆,而一超过室温就熔融。镓的化学活性低于铝,在常温下几 乎不受氧和水的侵蚀,只在高温下才被氧化;它与稀酸作用缓慢,可溶于热的强酸及强碱中,分别形成镓盐或镓酸盐;卤素与镓反应生成三卤化镓或一卤化镓;镓在 高温下能与硫、硒、碲、磷、砷、锑反应,生成的化合物都有半导体性质;镓的氧化和氢氧化物都是两性的,可溶于酸和碱中。镓可用作高温温度计和真空装置中的 密封液;镓的最重要的应用是在制造半导体器件方面;镓还用来制造阴极蒸汽灯等。

 

镓 - 高纯镓

高纯镓:high purity gallium,一般杂质总含量在10

高纯镓

-5 以下的金属镓。按镓含量分为5N,6N,7N和8N共四种级别。质软,淡蓝色光泽。熔点29.78℃。沸点2403℃。斜方晶型,各向异性显著。0℃的电 阻率沿a,b,c三个轴分别为1.75×10-6Ω•m,8.20×10-6Ω•m和55.30×10-6Ω•m。超纯镓剩余电阻率比值 ρ300K/ρ4.2K为55 000。采用化学处理、电解精炼、真空蒸馏、区域熔炼、拉单晶等多种工艺方法制备。主要用于电子工业和通讯领域,是制取各种镓化合物半导体的原料,硅、锗 半导体的掺杂剂,核反应堆的热交换介质。

 

镓 - 硝酸镓

分子 式:Ga(NO3)3•9H2O,用途:为制取镓化合物原料。性质:无色透明结晶体,易吸潮,空气中易分解。易溶于水,20℃时每100g水可溶解 295g,可溶于乙醇,但不溶于乙醚。102℃开始脱水,170℃完全分解,生成二氧化镓。由浓硝酸和氢氧化镓或金属镓作用制取。

 

镓 - 磷酸镓

 

磷酸镓:gallium phosphate

分子式:GaPO4•2H2O 

性质:白色无定形粉末,难溶于水(溶度积1.0×10-21)。140℃脱水。540℃转化为晶体。密度3.26g/cm3。熔点1670℃。和磷酸作用生成磷酸氢镓化合物。

制法:由镓盐溶液和碱金属磷酸盐在pH=5时反应制取。

 

镓 - 氧化镓

氧化镓别名三氧化二镓,氧化镓(Ga2O3)是一种宽禁带半导体,Eg=4

高纯试剂 氧化镓

.9eV,其导电性能和发光特性长期以来一直引起人们的注意。-Ga2O3是一种透明的氧化物半导体材料,在光电子器件方面有广阔的应用前景 ,被用作于Ga基半导体材料的绝缘层,以及紫外线滤光片。它还可以用作O2化学探测器。

 

 

镓 - 提炼

镓 在常温下,看上去象一块锡,如果你想把它放在手心里,它马上就熔化了,成为银亮的小珠。原来镓的熔点很低,只有29.8℃。镓的熔点虽然很低,可是沸点却 非常高,竟高达2070℃!人们就利用镓的这个特性来制造测量高温的温度计。把这种温度计伸进炉火熊熊的炼钢炉中,玻璃外壳都快熔化了,里边的镓还没有沸 腾,如果用耐高温的石英玻璃来制造镓温度计的外壳,它能够一直测到1500℃的高温。所以,人们常用这种温度计来测量反应炉、原子反应堆的温度。

 

镓具有较好的铸造特性,由于它“热缩冷胀”,被用来制造

金属镓

铅 字合金,使字体清晰。在原子能工业中,用镓作为热传导介质,把反应堆中的热量传导出来。 镓与许多金属,如铋、铅、锡、镉,铟、铊等,生成熔点低于60℃的易熔合金。其中如含铟25%的镓铟合金(熔点16℃),含锡8%的镓锡合金(熔点 20℃),可以用在电路熔断器和各种保险装置上,温度一高,它们就会自动熔化断开,起到安全保险的作用。

 

镓同玻璃合作,有增强玻璃折射率的效能,可以用来制造特种光学玻璃。因为镓对光的反射能力特别强,同时又能很好地附着在玻璃上,承受较高的温度,所以用它做反光镜最适宜,镓镜能把70%以上射来的光反射出去。

镓 的一些化合物,如今与尖端科学技术结下了不解之缘。砷化镓是近年来新发现的一种半导体材料,性能优良,用它作为电子元件,可以使电子设备的体积大为缩小, 实现微型化。人们还用砷化镓做元件制成了激光器,这是一种效率高、体积小的新型激光器。镓和磷的化合物——磷化镓是一种半导体发光元件,能够射出红光或绿 光,人们把它做成了各种阿拉伯数字形状,在电子计算机中,就利用它来显示计算结果。

 

引用出處: 

 http://www.hudong.com/wiki/%E9%95%93

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Gallium ( /ˈɡæliəm/ GAL-ee-əm) is a chemical element that has the symbol Ga and atomic number 31. Elemental gallium does not occur in nature, but as the gallium(III) salt in trace amounts in bauxite and zinc ores. A soft silvery metallic poor metal, elemental gallium is a brittle solid at low temperatures. As it liquefies slightly above room temperature, it will melt in the hand. Its melting point is used as a temperature reference point, and from its discovery in 1875 to the semiconductor era, its primary uses were in high-temperature thermometric applications and in preparation of metal alloys with unusual properties of stability, or ease of melting; some being liquid at room temperature or below. The alloy Galinstan (68.5% Ga, 21.5% In, 10% Sn) has a melting point of about −19 °C (−2 °F).

In semiconductors, the major-use compound is gallium arsenide used in microwave circuitry and infrared applications. Gallium nitride and indium gallium nitride, minority semiconductor uses, produce blue and violet light-emitting diodes (LEDs) and diode lasers. Semiconductor use is now almost the entire (> 95%) world market for gallium, but new uses in alloys and fuel cells continue to be discovered.

Gallium is not known to be essential in biology, but because of the biological handling of gallium's primary ionic salt gallium(III) as though it were iron(III), the gallium ion localizes to and interacts with many processes in the body in which iron(III) is manipulated. As these processes include inflammation, which is a marker for many disease states, several gallium salts are used, or are in development, as both pharmaceuticals and radiopharmaceuticals in medicine.

 

 

Contents

[hide]

  • 1 Notable characteristics
  • 2 History
  • 3 Occurrence
  • 4 Production
  • 5 Applications
    • 5.1 Semiconductors
    • 5.2 Wetting and alloy improvement
    • 5.3 Galinstan and other liquid alloys
    • 5.4 Energy storage
    • 5.5 Biomedical applications
      • 5.5.1 As gallium(III) salts
      • 5.5.2 As radiogallium salts
    • 5.6 Other uses
  • 6 Chemistry
    • 6.1 Chalcogen compounds
    • 6.2 Aqueous chemistry
    • 6.3 Pnictogen compounds
    • 6.4 Halides
    • 6.5 Hydrogen compounds
  • 7 Precautions
  • 8 See also
  • 9 References
  • 10 External links

[edit] Notable characteristics

Elemental gallium is not found in nature, but it is easily obtained by smelting. Very pure gallium metal has a brilliant silvery color and its solid metal fractures conchoidally like glass. Gallium metal expands by 3.1 percent when it solidifies, and therefore storage in either glass or metal containers is avoided, due to the possibility of container rupture with freezing. Gallium shares the higher-density liquid state with only a few materials like silicon, germanium, bismuth, antimony and water.

Gallium attacks most other metals by diffusing into their metal lattice. Gallium for example diffuses into the grain boundaries of Al/Zn alloys[1] or steel,[2] making them very brittle. Also, gallium metal easily alloys with many metals, and was used in small quantities as a plutonium-gallium alloy in the plutonium cores of the first and third nuclear bombs, to help stabilize the plutonium crystal structure.[3]

The melting point of 302.9146 K (29.7646°C, 85.5763°F) is near room temperature. Gallium's melting point (mp) is one of the formal temperature reference points in the International Temperature Scale of 1990 (ITS-90) established by BIPM.[4][5][6] The triple point of gallium of 302.9166 K (29.7666°C, 85.5799°F), is being used by NIST in preference to gallium's melting point.[7]

Gallium is a metal that will melt in one's hand. This metal has a strong tendency to supercool below its melting point/freezing point. Seeding with a crystal helps to initiate freezing. Gallium is one of the metals (with caesium, rubidium, francium and mercury) which are liquid at or near normal room temperature, and can therefore be used in metal-in-glass high-temperature thermometers. It is also notable for having one of the largest liquid ranges for a metal, and (unlike mercury) for having a low vapor pressure at high temperatures. Unlike mercury, liquid gallium metal wets glass and skin, making it mechanically more difficult to handle (even though it is substantially less toxic and requires far fewer precautions). For this reason as well as the metal contamination problem and freezing-expansion problems noted above, samples of gallium metal are usually supplied in polyethylene packets within other containers.

 

 

 

 

Crystallization of gallium from the melt

Gallium does not crystallize in any of the simple crystal structures. The stable phase under normal conditions is orthorhombic with 8 atoms in the conventional unit cell. Each atom has only one nearest neighbor (at a distance of 244 pm) and six other neighbors within additional 39 pm. Many stable and metastable phases are found as function of temperature and pressure.

The bonding between the nearest neighbors is found to be of covalent character, hence Ga2 dimers are seen as the fundamental building blocks of the crystal. This explains the drop of the melting point compared to its neighbour elements aluminium and indium. The compound with arsenic, gallium arsenide is a semiconductor commonly used in light-emitting diodes.

High-purity gallium is dissolved slowly by mineral acids.

Gallium has no known biological role, although it has been observed to stimulate metabolism.[8]

[edit] History

Gallium (the Latin Gallia means "Gaul", essentially modern France) was discovered spectroscopically by Paul Emile Lecoq de Boisbaudran in 1875 by its characteristic spectrum (two violet lines) in an examination of a zinc blende from the Pyrenees.[9] Before its discovery, most of its properties had been predicted and described by Dmitri Mendeleev (who had called the hypothetical element "eka-aluminium" on the basis of its position in his periodic table). Later, in 1875, Lecoq obtained the free metal by electrolysis of its hydroxide in potassium hydroxide solution. He named the element "gallia" after his native land of France. It was later claimed that, in one of those multilingual puns so beloved of men of science in the early 19th century, he had also named gallium after himself, as his name, "Le coq", is the French for "the rooster", and the Latin for "rooster" is "gallus"; however, in an 1877 article Lecoq denied this supposition.[10] (The supposition was also noted in Building Blocks of the Universe, a book on the elements by Isaac Asimov; cf. the naming of the J/ψ meson.)

[edit] Occurrence

Gallium does not exist in free form in nature, and the few high-gallium minerals such as gallite (CuGaS2) are too rare to serve as a primary source of the element or its compounds. Its abundance in the Earth's crust is approximately 16.9 ppm.[11] Gallium is found and extracted as a trace component in bauxite and to a small extent from sphalerite. The amount extracted from coal, diaspore and germanite in which gallium is also present is negligible. The United States Geological Survey (USGS) estimates gallium reserves to exceed 1 million tonnes, based on 50 ppm by weight concentration in known reserves of bauxite and zinc ores.[12][13] Some flue dusts from burning coal have been shown to contain small quantities of gallium, typically less than 1% by weight.[14][15][16][17]

[edit] Production

The only two economic sources for gallium are as byproduct of aluminium and zinc production, while the sphalerite for zinc production is the minor source. Most gallium is extracted from the crude aluminium hydroxide solution of the Bayer process for producing alumina and aluminium. A mercury cell electrolysis and hydrolysis of the amalgam with sodium hydroxide leads to sodium gallate. Electrolysis then gives gallium metal. For semiconductor use, further purification is carried out using zone melting, or else single crystal extraction from a melt (Czochralski process). Purities of 99.9999% are routinely achieved and commercially widely available.[18] An exact number for the world wide production is not available, but it is estimated that in 2007 the production of gallium was 184 tonnes with less than 100 tonnes from mining and the rest from scrap recycling.[12]

[edit] Applications

[edit] Semiconductors

 

 

 

 

Gallium based blue LEDs

 

 

 

 

Gallium phosphate crystal

The semiconductor applications are the main reason for the low-cost commercial availability of the extremely high-purity (99.9999+%) metal.

Gallium arsenide (GaAs) and gallium nitride (GaN) used in electronic components represented about 98% of the gallium consumption in the United States in 2007. About 66% of semiconductor gallium is used in the U.S. in integrated circuits (mostly gallium arsenide), such as the manufacture of ultra-high speed logic chips and MESFETs for low-noise microwave preamplifiers in cell phones. About 20% is used in optoelectronics.[12] World wide gallium arsenide makes up 95% of the annual global gallium consumption.[18]

Gallium arsenide is used in optoelectronics in a variety of infrared applications. Aluminium gallium arsenide (AlGaAs) is used in high-powered infrared laser diodes. As a component of the semiconductors indium gallium nitride and gallium nitride, gallium is used to produce blue and violet optoelectronic devices, mostly laser diodes and light-emitting diodes. For example, gallium nitride 405 nm diode lasers are used as a violet light source for higher-density compact disc data storage, in the Blu-ray Disc standard.[19]

Gallium is used as a dopant for the production of solid-state devices such as transistors. However, worldwide the actual quantity used for this purpose is minute, since dopant levels are usually of the order of a few parts per million.

Multijunction photovoltaic cells, developed for satellite power applications, are made by molecular beam epitaxy or metalorganic vapour phase epitaxy of thin films of gallium arsenide, indium gallium phosphide or indium gallium arsenide.The Mars Exploration Rovers and several satellites use triple junction gallium arsenide on germanium cells.[20] Gallium is the rarest component of new photovoltaic compounds (such as copper indium gallium selenium sulfide or Cu(In,Ga)(Se,S)2) for use in solar panels as a more efficient alternative to crystalline silicon.[21]

[edit] Wetting and alloy improvement

  • Because gallium wets glass or porcelain, gallium can be used to create brilliant mirrors. When the wetting action of gallium-alloys is not desired (as in Galinstan glass thermometers), the glass must be protected with a transparent layer of gallium(III) oxide.[22]
  • Gallium readily alloys with most metals, and has been used as a component in low-melting alloys. The plutonium used in nuclear weapon pits is machined by alloying with gallium to stabilize its δ phase.[23]
  • Gallium added in quantities up to 2% in common solders can aid wetting and flow characteristics.

[edit] Galinstan and other liquid alloys

A nearly eutectic alloy of gallium, indium, and tin is a room temperature liquid which is widely available in medical thermometers, replacing problematic mercury. This alloy, with the trade-name Galinstan (with the "-stan" referring to the tin), has a low freezing point of −19 °C (−2.2°F).[24] It has been suggested that this family of alloys could also be used to cool computer chips in place of water.[25] Much research is being devoted to gallium alloys as substitutes for mercury dental amalgams, but these compounds have yet to see wide acceptance.

[edit] Energy storage

Aluminium is reactive enough to reduce water to hydrogen, being oxidized to aluminium oxide. However, the aluminium oxide forms a protective coat which prevents further reaction. Galinstan has been applied to activate aluminium (removing the oxide coat), so that aluminium can react with water, generating hydrogen and steam in a reaction being considered as a helpful step in a hydrogen economy.[26][dubious – discuss] A number of other gallium-aluminium alloys are also usable for the purpose of essentially acting as chemical energy store to generate hydrogen from water, on-site.

After reaction with water the resultant aluminium oxide and gallium mixture must be reformed back into electrodes with energy input.[26][27] The thermodynamic efficiency of the aluminium smelting process is estimated as 50%.[28] Therefore, at most only half the energy that goes into smelting the aluminium could be recovered by a hydrogen fuel cell.

[edit] Biomedical applications

[edit] As gallium(III) salts

  • Gallium nitrate (brand name Ganite) has been used as an intravenous pharmaceutical to treat hypercalcemia associated with tumor metastasis to bones. Gallium is thought to interfere with osteoclast function. It may be effective when other treatments for maligancy-associated hypercalcemia are not.[29]
  • Gallium maltolate, an orally-aborbable form of gallium(III) ion, is in clinical and preclinical trials as a potential treatment for a number of types of cancer, infectious disease, and inflammatory disease.[30]
  • Research is being conducted to determine whether gallium ion can be used to fight bacterial infections in people with cystic fibrosis. Gallium is similar in size to iron, an essential nutrient for respiration. When gallium ions are mistakenly picked up by bacteria such as Pseudomonas, the bacteria's ability to respire is interfered with and the bacteria die. The mechanism behind this is that iron is redox active, which allows for the transfer of electrons during respiration, but gallium is redox inactive.[31][32]

[edit] As radiogallium salts

Gallium-67 salts such as gallium citrate and gallium nitrate are used as radiopharmaceutical agents in a nuclear medicine imaging procedure commonly referred to as a gallium scan. The form or salt of gallium is not important, since it is the free dissolved gallium ion Ga3+ which is the active radiotracer. For these applications, the radioactive isotope 67Ga is used. The body handles Ga3+ in many ways as though it were iron, and thus it is bound (and concentrates) in areas of inflammation, such as infection, and also areas of rapid cell division. This allows such sites to be imaged by nuclear scan techniques. This use has largely been replaced by fluorodeoxyglucose (FDG) for positron emission tomography, "PET" scan and indium-111 labelled leukocyte scans. However, the localization of gallium in the body has some properties which make it unique in some circumstances from competing modalities using other radioisotopes.

Gallium-68, a positron emitter with a half life of 68 min., is now used as a diagnostic radionuclide in CT-PET when linked to pharmaceutical preparations such as DOTATOC, a somatostatin analogue used for neuroendocrine tumors investigation, and DOTATATE, a newer one, used for neuroendocrine metastasis and lung neuroendocrine cancer, such as certain types of microcytoma. Galium-68's preparation as a pharmaceutical is chemical and the radionuclide is extracted by elution from germanium-68, a synthetic radioisotope of germanium, in gallium-68 generators.

[edit] Other uses

  • Magnesium gallate containing impurities (such as Mn2+), is beginning to be used in ultraviolet-activated phosphor powder.
  • Neutrino detection. Possibly the largest amount of pure gallium ever collected in a single spot is the Gallium-Germanium Neutrino Telescope used by the SAGE experiment at the Baksan Neutrino Observatory in Russia. This detector contains 55-57 tonnes of liquid gallium.[33] Another experiment was the GALLEX neutrino detector operated in the early 1990s in an Italian mountain tunnel. The detector contained 12.2 tons of watered gallium-71. Solar neutrinos caused a few atoms of Ga-71 to become radioactive Ge-71, which were detected. The solar neutrino flux deduced was found to have a deficit of 40% from theory. This was not explained until better solar neutrino detectors and theories were constructed (see SNO).[34]
  • As a liquid metal ion source for a focused ion beam.
  • As alloying element in the magnetic shape memory alloy Ni-Mn-Ga.
  • In a classic prank by scientists, who fashion gallium spoons and serve tea to unsuspecting guests. The spoons melt in the hot tea.[35]

[edit] Chemistry

Gallium is found primarily in the +3 oxidation state. The +1 oxidation is also attested in some compounds, although they tend to disproportionate into elemental gallium and gallium(III) compounds. What are sometimes referred to as gallium(II) compounds are actually mixed-oxidation state compounds containing both gallium(I) and gallium(III).[36]

[edit] Chalcogen compounds

At room temperature, gallium metal is unreactive towards air and water due to the formation of a passive, protective oxide layer. At higher temperatures, however, it reacts with oxygen in the air to form gallium(III) oxide, Ga2O3.[36] Reducing Ga2O3 with elemental gallium in vacuum at 500 °C to 700 °C yields the dark brown gallium(I) oxide, Ga2O.[37]:285 Ga2O is a very strong reducing agent, capable of reducing H2SO4 to H2S.[37]:207 It disproportionates at 800 °C back to gallium and Ga2O3.[38]

Gallium(III) sulfide, Ga2S3, has 3 possible crystal modifications.[38]:104 It can be made by the reaction of gallium with hydrogen sulfide (H2S) at 950 °C.[37]:162 Alternatively, Ga(OH)3 can also be used at 747 °C:[39]

 

2 Ga(OH)3 + 3 H2S → Ga2S3 + 6 H2O

Reacting a mixture of alkali metal carbonates and Ga2O3 with H2S leads to the formation of thiogallates containing the [Ga2S4]2− anion. Strong acids decompose these salts, releasing H2S in the process.[38]:104-105 The mercury salt, HgGa2S4, can be used as a phosphor.[40]

Gallium also forms sulfides in lower oxidation states, such as gallium(II) sulfide and the green gallium(I) sulfide, the latter of which is produced from the former by heating to 1000 °C under a stream of nitrogen.[38]:94

The other binary chalcogenides, Ga2Se3 and Ga2Te3, have zincblende structure. They are all semiconductors, but are easily hydrolysed, limiting their usefulness.[38]:104

[edit] Aqueous chemistry

Strong acids dissolve gallium, forming gallium(III) salts such as Ga2(SO4)3 and Ga(NO3)3. Aqueous solutions of gallium(III) salts contain the hydrated gallium ion, [Ga(H2O)6]3+.[41]:1033 Gallium(III) hydroxide, Ga(OH)3, may be precipitated from gallium(III) solutions by adding ammonia. Dehydrating Ga(OH)3 at 100 °C produces gallium oxide hydroxide, GaO(OH).[37]:140-141

 

Alkaline hydroxide solutions dissolve gallium, forming gallate salts containing the Ga(OH)−

4 anion.[36][41]:1033[42] Gallium hydroxide, which is amphoteric, also dissolves in alkali to form gallate salts.[37]:141 Although earlier work suggested Ga(OH)3−

6 as another possible gallate anion,[43] this species was not found in later work.[42]

[edit] Pnictogen compounds

Gallium reacts with ammonia at 1050 °C to form gallium nitride, GaN. Gallium also forms binary compounds with phosphorus, arsenic, and antimony: gallium phosphide (GaP), gallium arsenide (GaAs), and gallium antimonide (GaSb). These compounds have the same structure as ZnS, and have important semiconducting properties.[41]:1034 GaP, GaAs, and GaSb can be synthesized by the direct reaction of gallium with elemental phosphorus, arsenic, or antimony.[38]:99 They exhibit higher electrical conductivity than GaN.[38]:101 GaP can also be synthesized by the reaction of Ga2O with phosphorus at low temperatures.[44]

Gallium also forms ternary nitrides; for example:[38]:99

 

Li3Ga + N2 → Li3GaN2

Similar compounds with phosphorus and antimony also exist: Li3GaP2 and Li3GaAs2. These compounds are easily hydrolyzed by dilute acids and water.[38]:101

[edit] Halides

Gallium(III) oxide reacts with fluorinating agents such as HF or F2 to form gallium(III) fluoride, GaF3. It is an ionic compound strongly insoluble in water. However, it does dissolve in hydrofluoric acid, in which it forms an adduct with water, GaF3·3H2O. Attempting to dehydrate this adduct instead forms GaF2OH·nH2O. The adduct reacts with ammonia to form GaF3·3NH3, which can then be heated to form anhydrous GaF3.[37]:128-129

Gallium(III) chloride is formed by the reaction of gallium metal with chlorine gas.[36] Unlike the trifluoride, gallium(III) chloride exists as dimeric molecules, Ga2Cl6, with a melting point of 78 °C. This is also the case for the bromide and iodide, Ga2Br6 and Ga2I6.[37]:133

 

Like the other group 13 trihalides, gallium(III) halides are Lewis acids, reacting as halide acceptors with alkali metal halides to form salts containing GaX−

4 anions, where X is a halogen. They also react with alkyl halides to form carbocations and GaX−

4.[37]:136-137

When heated to a high temperature, gallium(III) halides react with elemental gallium to form the respective gallium(I) halides. For example, GaCl3 reacts with Ga to form GaCl:

 

2 Ga + GaCl3 3 GaCl (g)

At lower temperatures, the equilibrium shifts toward the left and GaCl disproportionates back to elemental gallium and GaCl3. GaCl can also be made by the reaction of Ga with HCl at 950 °C; it can then be condensed as red solid.[41]:1036

Gallium(I) compounds can be stabilized by forming adducts with Lewis acids. For example:

 

GaCl + AlCl3 → Ga+[AlCl4]−

The so-called "gallium(II) halides", GaX2, are actually adducts of gallium(I) halides with the respective gallium(III) halides, having the structure Ga+[GaX4]−. For example:[36][41]:1036[45]

 

GaCl + GaCl3 → Ga+[GaCl4]−

[edit] Hydrogen compounds

Like aluminium, gallium also forms a hydride, GaH3, known as gallane, which may be obtained by the reaction of lithium gallanate (LiGaH4) with gallium(III) chloride at −30 °C:[41]:1031

 

3 LiGaH4 + GaCl3 → 3 LiCl + 4 GaH3

In the presence of dimethyl ether as solvent, GaH3 polymerizes to (GaH3)n. If no solvent is used, the dimer Ga2H6 (digallane) is formed as a gas. Its structure is similar to diborane, having two hydrogen atoms bridging the two gallium centers,[41]:1031 unlike α-AlH3 in which aluminium has a coordination number of 6.[41]:1008

Gallane is unstable above −10 °C, decomposing to elemental gallium and hydrogen.[46]

[edit] Precautions

While not considered toxic, the data about gallium are inconclusive. Some sources suggest that it may cause dermatitis from prolonged exposure; other tests have not caused a positive reaction. Like most metals, finely divided gallium loses its luster and powdered gallium appears gray. Thus, when gallium is handled with bare hands, the extremely fine dispersion of liquid gallium droplets, which results from wetting skin with the metal, may appear as a gray skin stain.

 

引用出處: 

 http://en.wikipedia.org/wiki/Gallium

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BW Bewise Inc. Willy Chen willy@tool-tool.com  bw@tool-tool.com  www.tool-tool.com skype:willy_chen_bw mobile:0937-618-190 Head &Administration Office No.13,Shiang Shang 2nd St., West Chiu Taichung,Taiwan 40356 http://www.tool-tool.com/ / FAX:+886 4 2471 4839 N.Branch 5F,No.460,Fu Shin North Rd.,Taipei,Taiwan S.Branch No.24,Sec.1,Chia Pu East Rd.,Taipao City,Chiayi Hsien,Taiwan

Welcome to BW tool world! We are an experienced tool maker specialized in cutting tools. We focus on what you need and endeavor to research the best cutter to satisfy users demand. Our customers involve wide range of industries, like mold & die, aerospace, electronic, machinery, etc. We are professional expert in cutting field. We would like to solve every problem from you. Please feel free to contact us, its our pleasure to serve for you. BW product including: cutting toolaerospace tool .HSS  DIN Cutting toolCarbide end millsCarbide cutting toolNAS Cutting toolNAS986 NAS965 NAS897 NAS937orNAS907 Cutting Tools,Carbide end milldisc milling cutter,Aerospace cutting toolhss drillФрезерыCarbide drillHigh speed steelCompound SharpenerMilling cutterINDUCTORS FOR PCD’CVDD(Chemical Vapor Deposition Diamond )’PCBN (Polycrystalline Cubic Boron Nitride) Core drillTapered end millsCVD Diamond Tools Inserts’PCD Edge-Beveling Cutter(Golden FingerPCD V-CutterPCD Wood toolsPCD Cutting toolsPCD Circular Saw BladePVDD End Millsdiamond tool. INDUCTORS FOR PCD . POWDER FORMING MACHINE Single Crystal Diamond Metric end millsMiniature end millsСпециальные режущие инструменты Пустотелое сверло Pilot reamerFraisesFresas con mango PCD (Polycrystalline diamond) ‘FresePOWDER FORMING MACHINEElectronics cutterStep drillMetal cutting sawDouble margin drillGun barrelAngle milling cutterCarbide burrsCarbide tipped cutterChamfering toolIC card engraving cutterSide cutterStaple CutterPCD diamond cutter specialized in grooving floorsV-Cut PCD Circular Diamond Tipped Saw Blade with Indexable Insert PCD Diamond Tool Saw Blade with Indexable InsertNAS toolDIN or JIS toolSpecial toolMetal slitting sawsShell end millsSide and face milling cuttersSide chip clearance sawsLong end millsend mill grinderdrill grindersharpenerStub roughing end millsDovetail milling cuttersCarbide slot drillsCarbide torus cuttersAngel carbide end millsCarbide torus cuttersCarbide ball-nosed slot drillsMould cutterTool manufacturer. 

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BW специализируется в научных исследованиях и разработках, и снабжаем самым высокотехнологичным карбидовым материалом для поставки режущих / фрезеровочных инструментов для почвы, воздушного пространства и электронной индустрии. В нашу основную продукцию входит твердый карбид / быстрорежущая сталь, а также двигатели, микроэлектрические дрели, IC картонорезальные машины, фрезы для гравирования, режущие пилы, фрезеры-расширители, фрезеры-расширители с резцом, дрели, резаки форм для шлицевого вала / звездочки роликовой цепи, и специальные нано инструменты. Пожалуйста, посетите сайт  www.tool-tool.com  для получения большей информации.

BW is specialized in R&D and sourcing the most advanced carbide material with high-tech coating to supply cutting / milling tool for mould & die, aero space and electronic industry. Our main products include solid carbide / HSS end mills, micro electronic drill, IC card cutter, engraving cutter, shell end mills, cutting saw, reamer, thread reamer, leading drill, involute gear cutter for spur wheel, rack and worm milling cutter, thread milling cutter, form cutters for spline shaft/roller chain sprocket, and special tool, with nano grade. Please visit our web  www.tool-tool.com  for more info.

歡迎來到Bewise Inc.的世界,首先恭喜您來到這接受新的資訊讓產業更有競爭力,我們是提供專業刀具製造商,應對客戶高品質的刀具需求,我們可以協助客戶滿足您對產業的不同要求,我們有能力達到非常卓越的客戶需求品質,這是現有相關技術無法比擬的,我們成功的滿足了各行各業的要求,包括:精密HSS DIN切削刀具協助客戶設計刀具流程DIN or JIS 鎢鋼切削刀具設計NAS986 NAS965 NAS897 NAS937orNAS907 航太切削刀具,NAS航太刀具設計超高硬度的切削刀具醫療配件刀具設計複合式再研磨機PCD地板專用企口鑽石組合刀具粉末造粒成型機主機版專用頂級電桿PCBN刀具PCD刀具單晶刀具PCD V-Cut捨棄式圓鋸片組粉末成型機航空機械鉸刀主機版專用頂級電汽車業刀具設計電子產業鑽石刀具木工產業鑽石刀具銑刀與切斷複合再研磨機銑刀與鑽頭複合再研磨機銑刀與螺絲攻複合再研磨機等等。我們的產品涵蓋了從民生刀具到工業級的刀具設計;從微細刀具到大型刀具;從小型生產到大型量產;全自動整合;我們的技術可提供您連續生產的效能,我們整體的服務及卓越的技術,恭迎您親自體驗!!

BW Bewise Inc. Willy Chen willy@tool-tool.com  bw@tool-tool.com  www.tool-tool.com skype:willy_chen_bw mobile:0937-618-190 Head &Administration Office No.13,Shiang Shang 2nd St., West Chiu Taichung,Taiwan 40356 http://www.tool-tool.com/ / FAX:+886 4 2471 4839 N.Branch 5F,No.460,Fu Shin North Rd.,Taipei,Taiwan S.Branch No.24,Sec.1,Chia Pu East Rd.,Taipao City,Chiayi Hsien,Taiwan

Welcome to BW tool world! We are an experienced tool maker specialized in cutting tools. We focus on what you need and endeavor to research the best cutter to satisfy users demand. Our customers involve wide range of industries, like mold & die, aerospace, electronic, machinery, etc. We are professional expert in cutting field. We would like to solve every problem from you. Please feel free to contact us, its our pleasure to serve for you. BW product including: cutting toolaerospace tool .HSS  DIN Cutting toolCarbide end millsCarbide cutting toolNAS Cutting toolNAS986 NAS965 NAS897 NAS937orNAS907 Cutting Tools,Carbide end milldisc milling cutter,Aerospace cutting toolhss drillФрезерыCarbide drillHigh speed steelCompound SharpenerMilling cutterINDUCTORS FOR PCD’CVDD(Chemical Vapor Deposition Diamond )’PCBN (Polycrystalline Cubic Boron Nitride) Core drillTapered end millsCVD Diamond Tools Inserts’PCD Edge-Beveling Cutter(Golden FingerPCD V-CutterPCD Wood toolsPCD Cutting toolsPCD Circular Saw BladePVDD End Millsdiamond tool. INDUCTORS FOR PCD . POWDER FORMING MACHINE Single Crystal Diamond Metric end millsMiniature end millsСпециальные режущие инструменты Пустотелое сверло Pilot reamerFraisesFresas con mango PCD (Polycrystalline diamond) ‘FresePOWDER FORMING MACHINEElectronics cutterStep drillMetal cutting sawDouble margin drillGun barrelAngle milling cutterCarbide burrsCarbide tipped cutterChamfering toolIC card engraving cutterSide cutterStaple CutterPCD diamond cutter specialized in grooving floorsV-Cut PCD Circular Diamond Tipped Saw Blade with Indexable Insert PCD Diamond Tool Saw Blade with Indexable InsertNAS toolDIN or JIS toolSpecial toolMetal slitting sawsShell end millsSide and face milling cuttersSide chip clearance sawsLong end millsend mill grinderdrill grindersharpenerStub roughing end millsDovetail milling cuttersCarbide slot drillsCarbide torus cuttersAngel carbide end millsCarbide torus cuttersCarbide ball-nosed slot drillsMould cutterTool manufacturer.

Bewise Inc.  www.tool-tool.com

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情報を受け取って頂き、もっと各産業に競争力プラス展開。

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弊社は各領域に供給できる内容は:

(1)精密HSSエンドミルのR&D

(2)Carbide Cutting tools設計

(3)鎢鋼エンドミル設計

(4)航空エンドミル設計

(5)超高硬度エンドミル

(6)ダイヤモンドエンドミル

(7)医療用品エンドミル設計

(8)自動車部品&材料加工向けエンドミル設計

弊社の製品の供給調達機能は:

(1)生活産業~ハイテク工業までのエンドミル設計

(2)ミクロエンドミル~大型エンドミル供給

(3)小Lot生産~大量発注対応供給

(4)オートメーション整備調達

(5)スポット対応~流れ生産対応

弊社の全般供給体制及び技術自慢の総合専門製造メーカーに貴方のご体験を御待ちしております。   

Bewise Inc. talaşlı imalat sanayinde en fazla kullanılan ve üç eksende (x,y,z) talaş kaldırabilen freze takımlarından olan Parmak Freze imalatçısıdır. Çok geniş ürün yelpazesine sahip olan firmanın başlıca ürünlerini Karbür Parmak Frezeler, Kalıpçı Frezeleri, Kaba Talaş Frezeleri, Konik Alın Frezeler, Köşe Radyüs Frezeler, İki Ağızlı Kısa ve Uzun Küresel Frezeler, İç Bükey Frezeler vb. şeklinde sıralayabiliriz.

BW специализируется в научных исследованиях и разработках, и снабжаем самым высокотехнологичным карбидовым материалом для поставки режущих / фрезеровочных инструментов для почвы, воздушного пространства и электронной индустрии. В нашу основную продукцию входит твердый карбид / быстрорежущая сталь, а также двигатели, микроэлектрические дрели, IC картонорезальные машины, фрезы для гравирования, режущие пилы, фрезеры-расширители, фрезеры-расширители с резцом, дрели, резаки форм для шлицевого вала / звездочки роликовой цепи, и специальные нано инструменты. Пожалуйста, посетите сайт  www.tool-tool.com  для получения большей информации.

BW is specialized in R&D and sourcing the most advanced carbide material with high-tech coating to supply cutting / milling tool for mould & die, aero space and electronic industry. Our main products include solid carbide / HSS end mills, micro electronic drill, IC card cutter, engraving cutter, shell end mills, cutting saw, reamer, thread reamer, leading drill, involute gear cutter for spur wheel, rack and worm milling cutter, thread milling cutter, form cutters for spline shaft/roller chain sprocket, and special tool, with nano grade. Please visit our web  www.tool-tool.com  for more info.

 

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