2011年1月23日 星期日

铽 Tb www.tool-tool.com

铽,原子序数65,原子量158.92534,元素名来源于它的最初发现地。1843年瑞典化学家莫桑德尔从钇土中发现铽的氧化物,1877年正式命名。铽在地壳中的含量为十万分之九,存在于多种稀土矿物中,天然稳定同位素只有铽159。

纠错 编辑摘要

目录

  • 1 概述
  • 2 特性
  • 3 发现
  • 4 应用领域
  • 5 来源及用途
  • 1 概述
  • 2 特性
  • 3 发现
  • 4 应用领域
  • 5 来源及用途
  • 6 TB
  • 7 参考资料

铽 - 概述

铽为银灰色金属,有延展性,质较软,可用刀切开;熔点1360°C,沸点3123°C,密度8.2294克/厘米³;铽在室温下有很强的顺磁性。铽在空气中不易氧化,在高温时容易氧化;可与硫酸、硝酸、卤素反应。铽的氧化物广泛用于制备发光材料。

铽 - 特性

铽、Tb、65 、镧系元素

地壳中含量:(ppm):1.1

原子体积:(立方厘米/摩尔):19.2

周期, 元素分区 6, f

密度、硬度 8219 kg/m3、无数据

颜色和外表 银白色

元素在太阳中的含量:(ppm):0.0005

元素在海水中的含量:(ppm):太平洋表面 0.00000008

氧化铽

原子量 158.92534(2) 原子量单位

氧化态:Main Tb+3

Other Tb+4

原子半径(计算值) 175(225)pm

价电子排布 [氙]4f96s2

电子在每能级的排布 2,8,18,27,8,2

电离能 (kJ /mol)

M - M+ 564.6

M+ - M2+ 1112

M2+ - M3+ 2114

M3+ - M4+ 3839

晶体结构:晶胞为六方晶胞。

晶胞参数:

a = 360.1 pm

b = 360.1 pm

c = 569.36 pm

α = 90°

β = 90°

γ = 120°

维氏硬度:863MPa

声音在其中的传播速率:(m/S) 2620

氧化价(氧化物) 4(弱碱性)

晶体结构 六角形

物质状态 固态

熔点 1629 K(1356 °C)

沸点 3503 K (3230 °C)

摩尔体积 19.3×10-6m3/mol

汽化热 330.9 kJ/mol

熔化热 10.8 kJ/mol

声速 2620 m/s(293.15K)

电负性 1.2(鲍林标度)

比热 180 J/(kg•K)

电导率 0.889×106/(米欧姆)

热导率 11.1 W/(m•K)

第一电离能 565.8 kJ/mol

第二电离能 1110 kJ/mol

第三电离能 2114 kJ/mol

第四电离能 3839 kJ/mol

相对原子质量:158.925

常见化合价: +3,+4

电负性: 1.2

外围电子排布: 4f9 6s2

核外电子排布: 2,8,18,27,8,2

同位素及放射线: Tb-151[17.61h] Tb-155[5.3d] Tb-156[5.3d] Tb-157[110y] Tb-158[180y] Tb-159 Tb-160[72.3d] Tb-161[6.91d] Tb-162[7.6m]

最稳定的同位素 ,同位素 丰度 半衰期 衰变模式 衰变能量

MeV 衰变产物

157Tb 人造 71年 电子捕获 0.060 157Gd

158Tb 人造 180年 电子捕获

β衰变 1.220 0.937 158Gd 158Dy 159Tb 100 % 稳定

铽 - 发现

1843 年瑞典的莫桑德(Karl G.Mosander)通过对钇土的研究,发现铽元素(Terbium)。铽的应用大多涉及高技术领域,是技术密集、知识密集型的尖端项目,又是具有显著 经济效益的项目,有着诱人的发展前景。1843年由莫桑德尔(C.G.Mosander)发现。当初命名为氧化铒,1877年才正式命名为铽。1905年 第一次由乌贝因(G.Urbain)提纯制出。

在发现镧的同一时期里,莫桑德尔对最初发现的钇进行了分析研究,并于 1842年发表报告, 明确最初发现的钇土不是单一的元素氧化物,而是三种元素的氧化物。他把其中的一种仍称为钇土,其中一种命名为terbia(铽土)。元素符号定为Tb。它 的命名来源和钇一样,出自最初发现钇矿石的产地,瑞典斯德哥尔摩附近的小蛞姨乇龋╕tterby)。铽和另两个元素镧、铒的发现打开了发现稀土元素的第二 道大门,是发现稀土元素的第二阶段。他们的发现是继铈和钇两个元素后又找到稀土元素中的三个。一共是五个了。

铽 - 应用领域

1、荧光粉用于三基色荧光粉中的绿粉的激活剂,如铽激活的磷酸盐基质、铽激活的硅酸盐基质、铽激活的铈镁铝酸盐基质,在激发状态下均发出绿色光。

2、磁光贮存材料,近年来铽系磁光材料已达到大量生产的规

模,用Tb-Fe非晶态薄膜研制的磁光光盘,作计算机存储元件,存储能力提高10~15倍。

3、 磁光玻璃, 含铽的法拉第旋光玻璃是制造在激光技术中广泛应用的旋转器、隔离器和环形器的关键材料。特别是铽镝铁磁致伸缩合金(TerFenol)的开发研制,更是开 辟了铽的新用途,Terfenol是70年代才发现的新型材料,该合金中有一半成份为铽和镝,有时加入钬,其余为铁,该合金由美国依 阿华州阿姆斯实验室首先研制,当Terfenol置于一个磁场中时,其尺寸的变化比一般磁性材料变化大这种变化可以使一些精密机械运动得以实现。铽镝铁开 始主要用于声纳,目前已广泛应用于多种领域,从燃料喷射系统、液体阀门控制、微定位到机械致动器、机构和飞机太空望远镜的调节 机翼调节器等领域。

铽 - 来源及用途

元素描述:银灰色金属。高温下易被空气所腐蚀;室温下腐蚀极慢。溶于酸,盐类无色。氧化物Tb4O7是棕色。

元素来源:少量存在于磷铈钍砂和硅铍钇矿中。与其他稀土元素共存于独居石砂中,其中铽的含量一般为0.03%。其他来源还有磷钇矿和黑稀金矿,两者都是氧化物的混合物,含有高达1%的铽。

元素用途:用于制作高温燃料电池和激光材料。特种激光器和固态元件中用到少量的铽。

名称由来:得名于瑞典村庄Ytterby。

铽 - TB

结核是由结核杆菌引起的慢性肺部感染,咳嗽、胸痛、咯血、潮热、盗汗、消瘦、血沉增速为其主要临床特征。在人体抵抗力降低的情况下,因感染结核杆菌而发病,具传染性。

病原体及流行病学:

结核菌属于分支杆菌属,染色具有抗酸性,所以又叫抗酸杆菌。

氧化铽

能 引起人结核病的有两种,即人型结核菌和牛型结核菌,以人型为主。结核菌从病人或带菌者的呼吸道分泌物排出,并随灰尘飞扬于空中传与他人,尤其是开放型肺结 核患者,其痰液更是主要的传播来源。其次,咳嗽、喷嚏也可污染空气。牛型结核菌株可随其乳汁传播给人类。结核菌在阴湿处可生存6~8个月,但在沸水 中,15分钟即被杀死。

人体对结核菌抵抗力有两种,一为自然免疫力,即先天性非特异性免疫力,另一为对结核菌特有的免疫力,为感染结核后产生的特异性免疫力,也是后天获得性免疫力,多在两次感染后4~8周产生,产生后可使结核菌素试验呈阳性反应。结核杆菌易对抗痨药产生耐药性。

现代医学病理:结核菌侵入人体后,可长期寄生而不发病,当机体抗力薄弱时,或受感染病菌量多,或菌的毒力较强时则可发病。

TB是魔兽地图DOTA中灵魂守卫的英文缩写。

灵 魂守卫介 绍:Terrorblade - 灵魂守,Terrorblade和Magina原是孪生兄弟。虽然同样流着暗夜精灵的血,Terrorblade却受到不死族力量的诱惑而陷入不归的深 渊。背上巨大的石像鬼翅膀代表了他和暗夜世界的彻底决裂。他熟练的掌握了镜像的制造以及对灵魂的操纵。他可以变身为可怕而强大的恶魔,通过投掷能量打击对 手。挥舞着巨大月刃的他无疑是战场上的一大威慑。 初始射程 (Base Range): 100 | 初始攻击间隔 (Base Attack Time): 1.5

初始移动速度 (Base Move Speed): 320 | 初始防御 (Base Armor): 3.0

基本属性 (Primary Attribute): 敏捷 / Agility | 初始攻击力 (Base Damage): 48 - 54

初始力量值 (Base Strength): 15 | 初始敏捷值 (Base Agility): 22 | 初始智力值 (Base Intelligence): 15

力 量增长系数 (Strength Growth): 1.90 | 敏捷增长系数 (Agility Growth): 3.20 | 智力增长系数 (Intelligence Growth): 1.75 ,灵魂汲取 (Soul Steal) [E] ,魔法镜像 (Conjure Image) [C] ,变身 (Metamorphosis) [T] ,灵魂隔断 (Sunder)

引用出處:

http://www.hudong.com/wiki/%E9%93%BD

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Terbium www.tool-tool.com

Terbium ( /ˈtɜrbiəm/ TUR-bee-əm) is a chemical element with the symbol Tb and atomic number 65. It is a silvery-white rare earth metal that is malleable, ductile and soft enough to be cut with a knife. Terbium is never found in nature as a free element, but it is contained in many minerals, including cerite, gadolinite, monazite, xenotime and euxenite.

Terbium is used to dope calcium fluoride, calcium tungstate and strontium molybdate, materials that are used in solid-state devices, and as a crystal stabilizer of fuel cells which operate at elevated temperatures. As a component of Terfenol-D (an alloy that expands and contracts when exposed to magnetic fields more than any other alloy), terbium is of use in actuators, in naval sonar systems and in sensors.

The largest consumer of the world's terbium supply is in "green" phosphors (which are usually yellow). Terbium oxide is in fluorescent lamps and TV tubes. Terbium "green" phosphors (which fluoresce a brilliant lemon-yellow) are combined with divalent europium blue phosphors and trivalent europium red phosphors to provide "trichromatic" lighting technology, a high-efficiency white light used for standard illumination in indoor lighting.

Contents

[hide]

  • 1 Characteristics
    • 1.1 Physical properties
    • 1.2 Chemical properties
    • 1.3 Compounds
    • 1.4 Isotopes
  • 2 History
  • 3 Occurrence
  • 4 Production
  • 5 Applications
  • 6 Precautions
  • 7 References
  • 8 External links

[edit] Characteristics

[edit] Physical properties

Terbium is a silvery-white rare earth metal that is malleable, ductile and soft enough to be cut with a knife. It is relatively stable in air as compared to other lanthanides.[1] Terbium exists in two crystal allotropes with a transformation temperature of 1289 °C between them.[2]

The terbium(III) cation is brilliantly fluorescent, in a bright lemon-yellow color that is the result of a strong green emission line in combination with other lines in the orange and red. The yttrofluorite variety of the mineral fluorite owes its creamy-yellow fluorescence in part to terbium. Terbium easily oxidizes, and is therefore used in its elemental form specifically for research. Single Tb atoms have been isolated by implanting them into fullerene molecules.[3]

Terbium has a simple ferromagnetic ordering at temperatures below 219 K. Above 219 K, it turns into a helical antiferromagnetic state in which all of the atomic moments in a particular basal plane layer are parallel, and oriented at a fixed angle to the moments of adjacent layers. This unusual antiferromagnetism transforms into a disordered paramagnetic state at 230 K.[4]

[edit] Chemical properties

The most common valence state of terbium is +3, as in Tb2O3. The +4 state is known in TbO2 and TbF4.[5][6] Terbium burns readily to form a mixed terbium(III,IV) oxide:

8 Tb + 7 O2 → 2 Tb4O7

In solution, terbium forms only trivalent ions. Terbium is quite electropositive and reacts slowly with cold water and quite quickly with hot water to form terbium hydroxide:

2 Tb (s) + 6 H2O (l) → 2 Tb(OH)3 (aq) + 3H2 (g)

Terbium metal reacts with all the halogens:

2 Tb (s) + 3 F2 (g) → 2 TbF3 (s) [white]2 Tb (s) + 3 Cl2 (g) → 2 TbCl3 (s) [white]2 Tb (s) + 3 Br2 (g) → 2 TbBr3 (s) [white]2 Tb (s) + 3 I2 (g) → 2 TbI3 (s)

Terbium dissolves readily in dilute sulfuric acid to form solutions containing the pale pink Tb(III) ions, which exist as a [Tb(OH2)9]3+ complexes:[7]

2 Tb (s) + 3 H2SO4 (aq) → 2 Tb3+ (aq) + 3 SO2−

4 (aq) + 3 H2 (g)

[edit] Compounds

See also: Category:Terbium compounds

Terbium combines with nitrogen, carbon, sulfur, phosphorus, boron, selenium, silicon and arsenic at elevated temperatures, forming various binary compounds such as TbH2, TbH3, TbB2, Tb2S3, TbSe, TbTe and TbN.[6] In those compounds, Tb mostly exhibit oxidation states +3 and sometimes +2. Terbium(II) halogenides are obtained by annealing Tb(III) halogenides in presence of metallic Tb in tantalum containers. Terbium also forms sesquichloride Tb2Cl3, which can be further reduced to TbCl by annealing at 800 °C. This terbium(I) chloride forms platelets with layered graphite-like structure.[8]

Other compounds include

  • Chlorides: TbCl3
  • Bromides: TbBr3
  • Iodides: TbI3
  • Fluorides: TbF3, TbF4

Terbium(IV) fluoride is a strong fluorinating agent, emitting relatively pure atomic fluorine when heated[9] rather than the mixture of fluoride vapors emitted from CoF3 or CeF4.

[edit] Isotopes

Main article: isotopes of terbium

Naturally occurring terbium is composed of 1 stable isotope, 159Tb. 33 radioisotopes have been characterized, with the most stable being 158Tb with a half-life of 180 years, 157Tb with a half-life of 71 years, and 160Tb with a half-life of 72.3 days. All of the remaining radioactive isotopes have half-lives that are less than 6.907 days, and the majority of these have half-lives that are less than 24 seconds. This element also has 18 meta states, with the most stable being 156m1Tb (t½ 24.4 hours), 154m2Tb (t½ 22.7 hours) and 154m1Tb (t½ 9.4 hours).

The primary decay mode before the most abundant stable isotope, 159Tb, is electron capture, and the primary mode after is beta minus decay. The primary decay products before 159Tb are element Gd (gadolinium) isotopes, and the primary products after are element Dy (dysprosium) isotopes.

[edit] History

Terbium was discovered in 1843 by Swedish chemist Carl Gustaf Mosander, who detected it as an impurity in Yttrium oxide, Y2O3, and named after the village Ytterby in Sweden. It was not isolated in pure form until the recent advent of ion exchange techniques.[10]

When Mosander first partitioned "yttria" into three fractions, "terbia" was the fraction that contained the pink color (due to what is now known as erbium), and "erbia" was the fraction that was essentially colorless in solution, but gave a brown-tinged oxide. Later workers had difficulty in observing the latter, but the pink fraction was impossible to miss. Arguments went back and forth as to whether "erbia" even existed. In the confusion, the original names got reversed, and the exchange of names stuck. It is now thought that those workers who used the double sodium or potassium sulfates to remove "ceria" from "yttria" inadvertently lost the terbium content of the system into the ceria-containing precipitate. In any case, what is now known as terbium was only about 1% of the original yttria, but that was sufficient to impart a yellowish color to the oxide. Thus, terbium was a minor component in the original terbium fraction, dominated by its immediate neighbors, gadolinium and dysprosium. Thereafter, whenever other rare earths were teased apart from this mixture, whichever fraction gave the brown oxide retained the terbium name, until at last it was pure. The 19th century investigators did not have the benefit of fluorescence technology, wherewith to observe the brilliant fluorescence that would have made this element much easier to track in mixtures.[10]

[edit] Occurrence

Xenotime

Terbium is never found in nature as a free element, but it is contained in many minerals, including cerite, gadolinite, monazite ((Ce,La,Th,Nd,Y)PO4, which contains up to 0.03% of terbium), xenotime (YPO4) and euxenite ((Y,Ca,Er,La,Ce,U,Th)(Nb,Ta,Ti)2O6, which contains 1% or more of terbium). The crust abundance of terbium is estimated as 1.2 mg/kg.[6]

The richest current commercial sources of terbium are the ion-adsorption clays of southern China. The high-yttrium concentrate versions of these are about two-thirds yttrium oxide by weight, and about 1% terbia. However, small amounts occur in bastnäsite and monazite, and when these are processed by solvent-extraction to recover the valuable heavy lanthanides in the form of "samarium-europium-gadolinium concentrate" (SEG concentrate), the terbium content of the ore ends up therein. Due to the large volumes of bastnäsite processed, relative to the richer ion-adsorption clays, a significant proportion of the world's terbium supply comes from bastnäsite.[2]

[edit] Production

Crushed terbium-containing minerals are treated with hot concentrated sulfuric acid to produce water-soluble sulfates of rare earths. The acidic filtrates are partially neutralized with caustic soda to pH 3-4. Thorium precipitates out of solution as hydroxide and is removed. After that the solution is treated with ammonium oxalate to convert rare earths into their insoluble oxalates. The oxalates are converted to oxides by annealing. The oxides are dissolved in nitric acid that excludes one of the main components, cerium, whose oxide is insoluble in HNO3. Terbium is separated as a double salt with ammonium nitrate by crystallization.[6]

The most efficient separation routine for terbium salt from the rare-earth salt solution is ion exchange. In this process, rare-earth ions are sorbed onto suitable ion-exchange resin by exchange with hydrogen, ammonium or cupric ions present in the resin. The rare earth ions are then selectively washed out by suitable complexing agent. As with other rare earths, terbium metal is produced by reducing the anhydrous chloride or fluoride with calcium metal. Calcium and tantalum impurities can be removed by vacuum remelting, distillation, amalgam formation or zone melting.[6]

[edit] Applications

Terbium is used as a Dopant in calcium fluoride, calcium tungstate and strontium molybdate, materials that are used in solid-state devices, and as a crystal stabilizer of fuel cells which operate at elevated temperatures, together with ZrO2.[2]

Terbium is also used in alloys and in the production of electronic devices. As a component of Terfenol-D, terbium is of use in actuators, in naval sonar systems, sensors, in the SoundBug device (its first commercial application), and other magnetomechanical devices. Terfenol-D is an alloy that expands or contracts in the presence of a magnetic field. It has the highest magnetostriction of any alloy.[11]

Terbium oxide is used in green phosphors in fluorescent lamps and color TV tubes. Sodium terbium borate is used in solid state devices. The brilliant fluorescence allows terbium to be used as a probe in biochemistry, where it somewhat resembles calcium in its behavior. Terbium "green" phosphors (which fluoresce a brilliant lemon-yellow) are combined with divalent europium blue phosphors and trivalent europium red phosphors to provide the "trichromatic" lighting technology which is by far the largest consumer of the world's terbium supply. Trichromatic lighting provides much higher light output for a given amount of electrical energy than does incandescent lighting.[2]

[edit] Precautions

As with the other lanthanides, terbium compounds are of low to moderate toxicity, although their toxicity has not been investigated in detail. Terbium has no known biological role.[2]

引用出處:

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

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Terbium www.tool-tool.com

Terbium ( /ˈtɜrbiəm/ TUR-bee-əm) is a chemical element with the symbol Tb and atomic number 65. It is a silvery-white rare earth metal that is malleable, ductile and soft enough to be cut with a knife. Terbium is never found in nature as a free element, but it is contained in many minerals, including cerite, gadolinite, monazite, xenotime and euxenite.

Terbium is used to dope calcium fluoride, calcium tungstate and strontium molybdate, materials that are used in solid-state devices, and as a crystal stabilizer of fuel cells which operate at elevated temperatures. As a component of Terfenol-D (an alloy that expands and contracts when exposed to magnetic fields more than any other alloy), terbium is of use in actuators, in naval sonar systems and in sensors.

The largest consumer of the world's terbium supply is in "green" phosphors (which are usually yellow). Terbium oxide is in fluorescent lamps and TV tubes. Terbium "green" phosphors (which fluoresce a brilliant lemon-yellow) are combined with divalent europium blue phosphors and trivalent europium red phosphors to provide "trichromatic" lighting technology, a high-efficiency white light used for standard illumination in indoor lighting.

Contents

[hide]

  • 1 Characteristics
    • 1.1 Physical properties
    • 1.2 Chemical properties
    • 1.3 Compounds
    • 1.4 Isotopes
  • 2 History
  • 3 Occurrence
  • 4 Production
  • 5 Applications
  • 6 Precautions
  • 7 References
  • 8 External links

[edit] Characteristics

[edit] Physical properties

Terbium is a silvery-white rare earth metal that is malleable, ductile and soft enough to be cut with a knife. It is relatively stable in air as compared to other lanthanides.[1] Terbium exists in two crystal allotropes with a transformation temperature of 1289 °C between them.[2]

The terbium(III) cation is brilliantly fluorescent, in a bright lemon-yellow color that is the result of a strong green emission line in combination with other lines in the orange and red. The yttrofluorite variety of the mineral fluorite owes its creamy-yellow fluorescence in part to terbium. Terbium easily oxidizes, and is therefore used in its elemental form specifically for research. Single Tb atoms have been isolated by implanting them into fullerene molecules.[3]

Terbium has a simple ferromagnetic ordering at temperatures below 219 K. Above 219 K, it turns into a helical antiferromagnetic state in which all of the atomic moments in a particular basal plane layer are parallel, and oriented at a fixed angle to the moments of adjacent layers. This unusual antiferromagnetism transforms into a disordered paramagnetic state at 230 K.[4]

[edit] Chemical properties

The most common valence state of terbium is +3, as in Tb2O3. The +4 state is known in TbO2 and TbF4.[5][6] Terbium burns readily to form a mixed terbium(III,IV) oxide:

8 Tb + 7 O2 → 2 Tb4O7

In solution, terbium forms only trivalent ions. Terbium is quite electropositive and reacts slowly with cold water and quite quickly with hot water to form terbium hydroxide:

2 Tb (s) + 6 H2O (l) → 2 Tb(OH)3 (aq) + 3H2 (g)

Terbium metal reacts with all the halogens:

2 Tb (s) + 3 F2 (g) → 2 TbF3 (s) [white]2 Tb (s) + 3 Cl2 (g) → 2 TbCl3 (s) [white]2 Tb (s) + 3 Br2 (g) → 2 TbBr3 (s) [white]2 Tb (s) + 3 I2 (g) → 2 TbI3 (s)

Terbium dissolves readily in dilute sulfuric acid to form solutions containing the pale pink Tb(III) ions, which exist as a [Tb(OH2)9]3+ complexes:[7]

2 Tb (s) + 3 H2SO4 (aq) → 2 Tb3+ (aq) + 3 SO2−

4 (aq) + 3 H2 (g)

[edit] Compounds

See also: Category:Terbium compounds

Terbium combines with nitrogen, carbon, sulfur, phosphorus, boron, selenium, silicon and arsenic at elevated temperatures, forming various binary compounds such as TbH2, TbH3, TbB2, Tb2S3, TbSe, TbTe and TbN.[6] In those compounds, Tb mostly exhibit oxidation states +3 and sometimes +2. Terbium(II) halogenides are obtained by annealing Tb(III) halogenides in presence of metallic Tb in tantalum containers. Terbium also forms sesquichloride Tb2Cl3, which can be further reduced to TbCl by annealing at 800 °C. This terbium(I) chloride forms platelets with layered graphite-like structure.[8]

Other compounds include

  • Chlorides: TbCl3
  • Bromides: TbBr3
  • Iodides: TbI3
  • Fluorides: TbF3, TbF4

Terbium(IV) fluoride is a strong fluorinating agent, emitting relatively pure atomic fluorine when heated[9] rather than the mixture of fluoride vapors emitted from CoF3 or CeF4.

[edit] Isotopes

Main article: isotopes of terbium

Naturally occurring terbium is composed of 1 stable isotope, 159Tb. 33 radioisotopes have been characterized, with the most stable being 158Tb with a half-life of 180 years, 157Tb with a half-life of 71 years, and 160Tb with a half-life of 72.3 days. All of the remaining radioactive isotopes have half-lives that are less than 6.907 days, and the majority of these have half-lives that are less than 24 seconds. This element also has 18 meta states, with the most stable being 156m1Tb (t½ 24.4 hours), 154m2Tb (t½ 22.7 hours) and 154m1Tb (t½ 9.4 hours).

The primary decay mode before the most abundant stable isotope, 159Tb, is electron capture, and the primary mode after is beta minus decay. The primary decay products before 159Tb are element Gd (gadolinium) isotopes, and the primary products after are element Dy (dysprosium) isotopes.

[edit] History

Terbium was discovered in 1843 by Swedish chemist Carl Gustaf Mosander, who detected it as an impurity in Yttrium oxide, Y2O3, and named after the village Ytterby in Sweden. It was not isolated in pure form until the recent advent of ion exchange techniques.[10]

When Mosander first partitioned "yttria" into three fractions, "terbia" was the fraction that contained the pink color (due to what is now known as erbium), and "erbia" was the fraction that was essentially colorless in solution, but gave a brown-tinged oxide. Later workers had difficulty in observing the latter, but the pink fraction was impossible to miss. Arguments went back and forth as to whether "erbia" even existed. In the confusion, the original names got reversed, and the exchange of names stuck. It is now thought that those workers who used the double sodium or potassium sulfates to remove "ceria" from "yttria" inadvertently lost the terbium content of the system into the ceria-containing precipitate. In any case, what is now known as terbium was only about 1% of the original yttria, but that was sufficient to impart a yellowish color to the oxide. Thus, terbium was a minor component in the original terbium fraction, dominated by its immediate neighbors, gadolinium and dysprosium. Thereafter, whenever other rare earths were teased apart from this mixture, whichever fraction gave the brown oxide retained the terbium name, until at last it was pure. The 19th century investigators did not have the benefit of fluorescence technology, wherewith to observe the brilliant fluorescence that would have made this element much easier to track in mixtures.[10]

[edit] Occurrence

Xenotime

Terbium is never found in nature as a free element, but it is contained in many minerals, including cerite, gadolinite, monazite ((Ce,La,Th,Nd,Y)PO4, which contains up to 0.03% of terbium), xenotime (YPO4) and euxenite ((Y,Ca,Er,La,Ce,U,Th)(Nb,Ta,Ti)2O6, which contains 1% or more of terbium). The crust abundance of terbium is estimated as 1.2 mg/kg.[6]

The richest current commercial sources of terbium are the ion-adsorption clays of southern China. The high-yttrium concentrate versions of these are about two-thirds yttrium oxide by weight, and about 1% terbia. However, small amounts occur in bastnäsite and monazite, and when these are processed by solvent-extraction to recover the valuable heavy lanthanides in the form of "samarium-europium-gadolinium concentrate" (SEG concentrate), the terbium content of the ore ends up therein. Due to the large volumes of bastnäsite processed, relative to the richer ion-adsorption clays, a significant proportion of the world's terbium supply comes from bastnäsite.[2]

[edit] Production

Crushed terbium-containing minerals are treated with hot concentrated sulfuric acid to produce water-soluble sulfates of rare earths. The acidic filtrates are partially neutralized with caustic soda to pH 3-4. Thorium precipitates out of solution as hydroxide and is removed. After that the solution is treated with ammonium oxalate to convert rare earths into their insoluble oxalates. The oxalates are converted to oxides by annealing. The oxides are dissolved in nitric acid that excludes one of the main components, cerium, whose oxide is insoluble in HNO3. Terbium is separated as a double salt with ammonium nitrate by crystallization.[6]

The most efficient separation routine for terbium salt from the rare-earth salt solution is ion exchange. In this process, rare-earth ions are sorbed onto suitable ion-exchange resin by exchange with hydrogen, ammonium or cupric ions present in the resin. The rare earth ions are then selectively washed out by suitable complexing agent. As with other rare earths, terbium metal is produced by reducing the anhydrous chloride or fluoride with calcium metal. Calcium and tantalum impurities can be removed by vacuum remelting, distillation, amalgam formation or zone melting.[6]

[edit] Applications

Terbium is used as a Dopant in calcium fluoride, calcium tungstate and strontium molybdate, materials that are used in solid-state devices, and as a crystal stabilizer of fuel cells which operate at elevated temperatures, together with ZrO2.[2]

Terbium is also used in alloys and in the production of electronic devices. As a component of Terfenol-D, terbium is of use in actuators, in naval sonar systems, sensors, in the SoundBug device (its first commercial application), and other magnetomechanical devices. Terfenol-D is an alloy that expands or contracts in the presence of a magnetic field. It has the highest magnetostriction of any alloy.[11]

Terbium oxide is used in green phosphors in fluorescent lamps and color TV tubes. Sodium terbium borate is used in solid state devices. The brilliant fluorescence allows terbium to be used as a probe in biochemistry, where it somewhat resembles calcium in its behavior. Terbium "green" phosphors (which fluoresce a brilliant lemon-yellow) are combined with divalent europium blue phosphors and trivalent europium red phosphors to provide the "trichromatic" lighting technology which is by far the largest consumer of the world's terbium supply. Trichromatic lighting provides much higher light output for a given amount of electrical energy than does incandescent lighting.[2]

[edit] Precautions

As with the other lanthanides, terbium compounds are of low to moderate toxicity, although their toxicity has not been investigated in detail. Terbium has no known biological role.[2]

引用出處:

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

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!!

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鑽石冶煉術www.tool-tool.com

摘要】提到「鑽石」──這人見人愛,燦爛奪目的寶石,每個人莫不怦然心動。但是您知這嗎?在它背後所蘊含的科學,更值得我們來探討。

1955 年冬天的某個下午,在美國紐約州史奈他地(Schenectady)鎮,從奇異公司研究發展中心大門,駛出一輛汽 車,車子主人溫特夫(R.Wentorf Jr.),神色興奮地在附近的雜貨鋪買了一瓶花生醬回來,然後當晚在該中心高壓實驗中,成功地利用花生醬製造出「鑽石粒」。從此展開了鑽石新的生命。

溫 特夫等人製造鑽石的程序,是運用高壓(4~6萬大氣壓)、高溫(1700K)和長時間的反應,類似天然鑽石在地球內部形成 的條件。而不同的條件和觸媒劑可以合成出性質和大小不同的鑽石,所以奇異公司位於俄亥俄州渥興頓市(Wothington)的超級研磨中心,至今仍是世界 上製造人造鑽石和其他研磨材料的領導者。

為什麼學科學的我們要談「合成鑽石」呢?我們不是企求價昂的寶石賣錢,而是希望能開發出鑽石在科 學中的應用。我們知道鑽石是 地球上已知最硬和傳熱最快的物質,所以它可以用來切割或研磨其他任何物體,至於傳熱的性質則一直未曾應用,一直要到1970年代末期人們才開始用到(請參 閱本刊十八卷九期〈從石刀石斧到太空梭〉一文)。

話說CVD

1960年,一個以德雅金(B.Deryaguin)為首的蘇 俄研究群,成功地利用「化學氣態蒸鍍法」(chemical vapor deposition, CVD)合成出「鑽石薄膜」,但是因為薄膜成長速率極低(0.01微米/每小時),沒有引起人注意。到了1976年德雅金等人又說,他們可以每小時一個微 米的成長厚度來合成鑽石薄膜,但是對詳細的程序條件卻守口如瓶。此舉引不起全世界有關研究者的注意力,其實這其中還牽涉到旁人對於德雅金小組的研究態度的 持疑。因為在1970年代初期,德雅金宣稱他們發現了一種聚合態的水,而令人害怕的是海洋的水很可能某一時候會轉變成此種聚合態水,引起當時人們憂心忡 忡,真是世界末日來到。可是不久之後大家證明德雅金的發現純屬無稽之談,就因為這樣,數年之後,當德雅金宣稱成長速率可以達到每小時1微米時,沒有人願意 相信和接受。

但是終究有人把德雅金的話當真,日本的研究團體很認真地重複德雅金的實驗;1982年開始,日本國立無機材科研究所的科學 家,陸續發表了數篇有關CVD鑽石技術的文章,文中很明確地指出:在何種狀態之下可以達到德雅金的速率。接著全世界其他地方的科學家,都重複出日本的實驗 結果;到了此時,所謂「鑽石熱」就在全世界各地燃燒起來了,人們也開始利用到鑽石的傳熱性質。

什麼是CVD呢?

CVD技術 其實十分簡單(見圖一),首先把氫氣和含碳氫氣體(通常是甲烷)通過氣體調節器之後,輸入到已抽至低壓(10-3torr) 的反應室內(兩種氣體的比例可以經由調節器控制),然後用電熱絲或微波源,或者無線電波源(RF)來加熱混合氣體至2000℃;在這個溫度下,氫氣和甲烷 會分解成氫原子和碳原子形成電漿流,然後碳原子會在已熱至600~1000℃的基質上,結核長膜。而剩下的廢氣,用真空抽氣機抽至室外,以避危險(氫氣會 自燃)。

很奇怪的是氫原子在這過程中的角色。既然鑽石是純碳結構,為何還需要氫氣呢?大部分的研究者認為,氫原子扮演了舉足輕重的角色。 我們從化學課本中可知道,在鑽石中每一個碳原子和其他四個鄰近碳原子,各以共價鍵相連(sp3立體結構);如果在CVD成核階段時,沒有足夠的碳原子來結 成sp3立體結構,那很可能會以sp2平面結構的石墨出現(見圖二),而氫原子的功用是能把未被結合成sp3立體結構的多餘碳原子聯起來,不讓它跑掉,直 到另外的碳原子來取代它的地位,然後讓氫原子跑走。

照以上的描述,也許你會推論:大量增加碳原子的數目(甲烷的分量),應該會加快碳原子結 核速率。但是實際上,目前已知最好成 長速率的實驗狀態是:甲烷占總氣體體積(甲烷加氫氣)的0.5~1.5%。鑽石的形成似乎存在一個自然法則,而我們絲毫不知。雖然我們對於鑽石形成的詳細 機制無法確知,但是大家並不氣餒,反而更積極地嘗試錯誤,不斷改進;仔細想起來是有點好笑,就像一位廚房新手在做菜一樣,不知道要加多少調味料才會好吃; 於是一時之間,科學家儼然變成現代的「煉金師」了。

高明的「試金石」

在基質上合成的物質如何知道就是鑽石呢?這是很重要的 一步,通常我們用下列數種方法來驗證:硬度試驗、掃描式電子顯微儀 (SEM)、X射線繞射法、拉曼頻譜(Raman spectroscopy)和反射式高能電子繞射法(RHEED)。在此筆者並不解釋幾種方法原理,而僅提出有關試驗鑽石的結果。

硬度試驗 是利用微維克(micro-Vicker)方法,來測定合成物的硬度是否達到天然鑽石的硬度值 ──7,000~10,000公斤/平方毫米。因為這個方法簡單易測,所以通常是第一個採取的檢測方法,如果檢測出硬度值在標準範圍內,則從事進一步較精 確的檢測方法;如果不在期望值之內,那就把它丟在一旁吧。

要測定鑽石,在1960年代時還是一項費時而困難的工作,即使在今日我們還是必 須非常小心的;1986年日本大阪大學的研究 群(K.Kitahama為首)發表文章說:他們在40~800℃之間用雷射光當做熱源,成功地合成了鑽石,他們用了電子繞射法來驗證結果。如果這是真的 話,那確是一項鑽石技術上的一個突破(尤其是在接近室溫)。但是直到1988年末,其他的研究者才用了拉曼頻譜術,證明大阪大學的結果是錯誤的。因為鑽石 和石墨的電子繞射譜是挺相似的,所以單是電子(或X光)繞射法不足以完完全全證明鑽石。

我們在此為鑽石下一個操作型定義:真正的鑽石鍍膜必須用掃描式或穿隧式電子顯微儀檢明結晶結構,並用X射線或電子繞射法檢查單相晶體結構,再用拉曼頻譜術檢查出強而窄的1332cm-1譜線。

圖 三是鑽石在掃描式電子顯微鏡下的樣子,圖四是立方鑽石的X射線繞射圖樣,我們可以從圖樣中計算出結晶平面的間距,然後拿此 數據與美國物質測試學會(ASTM)的基本鑽石資料比對,即可得知大概。而RHEED方法得出之數據與此相同,亦可拿來比對;圖五是鑽石RHEED的繞射 條紋和數據對照。拉曼頻譜術對於任何類似鑽石而非鑽石的結構特別有用,所以用它來測量鑽石薄膜的完美性是很理想的。圖六是天然鑽石,高品質合成鑽石薄膜和 含石墨的鑽石薄膜的拉曼頻譜比較。

鑽石極品,無與倫比

雖然大部分的研究者都還在研究鑽石CVD鍍膜技術,但是已經有商業化的CVD產品問世了,在此略舉數件,讀者便知道它的好處了。

第 一件商業CVD產品是日本JVC出產的高頻揚聲器,他們把類鑽石鍍在揚聲器中的振動膜上,因鑽石具高傳聲速度、高頑抗性和 低重量之性質,使它更容易振動出更高頻的聲音,於是高頻失真性大為減低,只是它的價格昂貴,只供專業人士使用。美國加州Crystallume公司出產一 種X射線(或紅外線)光窗,因為鑽石對於X射線(及可見光)的高透明性,所以使得分析物質中例如碳、氮和氧之工作更為便利(見圖七)。另外,日本精工公司 計畫推出表殼玻璃上鍍著鑽石的表,你可以想像得出那種表耐磨又防老化。

同時我們可以猜想得出其他尚未問世的產品,例如把鑽石鍍在眼鏡片 上,既防磨損又摔不破;我們也可以製造出非常大而薄的玻璃 窗,只要把鑽石鍍在表面,那我們便不怕它易碎了。因為鑽石的折射率(n=2.42)很高,我們可以用它來當做過濾片或者防止反射的薄膜,以致我們可以把它 應用在光通訊、光計算和積體光學等方面。

當然鑽石薄膜在半導體工業方面的應用是較受人注意的,高密度的積體電路是希望能把電子行走路線縮 短以增快訊號傳輸速率。但是 這有幾點困難:電磁波干涉(暫且不論)和散熱率不好;我們在使用學校大電腦時,經常會遇到莫名其妙的當機,大部分是因為機器散熱不佳以致當機;如果我們把 鑽石鍍膜技術用到積體電路上,增加每個晶片的散熱性,將會大大增加現有電腦的可靠性,並會改變未來積體電路的設計原則。

鑽石技術是新而有 潛力的研究領域,往往靠著個人的靈機一動即可帶來新的突破;1990年七月奇異公司宣布,它利用本身已有的 製造鑽石粒之高壓技術和現今的CVD合成鑽石技術,成功地合成出比天然鑽石傳熱性更快,且不受雷射光損傷的鑽石,因而轟動一時。1988年,日本幾位研究 者更是厲害,他們在大氣壓力之下使用氧乙炔(銲接用),在950℃時成功合成出單晶或複晶狀鑽石,令人叫絕(見圖八)。

圖九是一棵「鑽石 樹」,說明鑽石合成技術是以化學、物理工程學和材料科學為根基,而它的應用分支十分的多。依照筆者接觸所 及,認為涉及之實驗設備並不昂貴,所占空間也不大,適合小的研究組來研究,如果假以時日,持續不斷地做,必會覺得這是一個投資報酬率高且一本萬利的事業。

參考資料:

1.Boggs R., 1989, "Diamond thin film", Design News,70~75, April 10.

2.Amato I., 1990, "Diamond fever", Science News, 138:72~74, August 4.

3.Bachmann P. and Messier R., 1989, " Enering technology diamond thinfilms", C & EN, 24~39, May 15.

4.Matsumoto S. et. al., 1982, "Vapor deposition of diamond particles from methane", JJAP, 21: 183~185, April.

楊天行就讀於美國麻州羅威爾大學物理系研究所

引用出處:

http://campus2.chgsh.chc.edu.tw/science/content/1991/00010253/0007.htm

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Gadolinium www.tool-tool.com

Gadolinium ( /ˌɡædɵˈlɪniəm/ GAD-o-LIN-ee-əm) is a chemical element with the symbol Gd and atomic number 64. It is a silvery-white, malleable and ductile rare-earth metal. Gadolinium has exceptionally high absorption of neutrons and therefore is used for shielding in neutron radiography and in nuclear reactors. Because of its paramagnetic properties, solutions of organic gadolinium complexes and gadolinium compounds are the most popular intravenous MRI contrast agents in medical magnetic resonance imaging.

Contents

[hide]

  • 1 Characteristics
    • 1.1 Physical properties
    • 1.2 Chemical properties
    • 1.3 Lower oxidation state derivatives
    • 1.4 Compounds
    • 1.5 Isotopes
  • 2 History
  • 3 Occurrence
  • 4 Production
  • 5 Applications
  • 6 Biological role
  • 7 Safety
  • 8 References
  • 9 External links

[edit] Characteristics

A sample of gadolinium

[edit] Physical properties

Gadolinium is a silvery-white malleable and ductile rare-earth metal. It crystallizes in hexagonal, close-packed α- form at room temperature, but, when heated to temperatures above 1235 °C, it transforms into its β- form, which has a body-centered cubic structure.[2]

Gadolinium-157 has the highest thermal neutron capture cross-section among any stable nuclides: 259,000 barns. Only xenon-135 has a higher cross section, 2 million barns, but that isotope is unstable.[3]

Gadolinium is a ferromagnetic at temperatures below 19 °C and is strongly paramagnetic above this temperature. Whereas it is normally a metal, it becomes a ferromagnetic superconductor at temperatures below 1.083 K.[4] Gadolinium demonstrates a magnetocaloric effect whereby its temperature increases when it enters a magnetic field and decreases when it leaves the magnetic field. The effect is considerably stronger for the gadolinium alloy Gd5(Si2Ge2).[5]

Individual gadolinium atoms have been isolated by encapsulating them into fullerene molecules and visualized with transmission electron microscope.[6] Individual Gd atoms and small Gd clusters have also been incorporated into carbon nanotubes.[7]

[edit] Chemical properties

Unlike other rare earth elements, metallic gadolinium is relatively stable in dry air. However, it tarnishes quickly in moist air, forming a loosely adhering oxide which spalls off, exposing more surface to oxidation.

4 Gd + 3 O2 → 2 Gd2O3

Gadolinium is a strong reducing agent, which reduces oxides of several metals, such as Fe, Cr, Sn, Pb, Mn and Zr, into their elements.[2] Gadolinium is quite electropositive and reacts slowly with cold water and quite quickly with hot water to form gadolinium hydroxide:

2 Gd + 6 H2O → 2 Gd(OH)3 + 3 H2

Gadolinium dissolves readily in dilute sulfuric acid to form solutions containing the colorless Gd(III) ions, which exist as a [Gd(OH2)9]3+ complexes:[8]

2 Gd (s) + 3 H2SO4 (aq) → 2 Gd3+ (aq) + 3 SO2−

4 (aq) + 3 H2 (g)

Gadolinium metal reacts with all of the halogens at temperature about 200 °C:

2 Gd (s) + 3 F2 (g) → 2 GdF3 (s) [white]2 Gd (s) + 3 Cl2 (g) → 2 GdCl3 (s) [white]2 Gd (s) + 3 Br2 (g) → 2 GdBr3 (s) [white]2 Gd (s) + 3 I2 (g) → 2 GdI3 (s) [yellow]

Gadolinium combines with nitrogen, carbon, sulfur, phosphorus, boron, selenium, silicon and arsenic at elevated temperatures, forming binary compounds.[2]

[edit] Lower oxidation state derivatives

In the great majority of its compounds, Gd has oxidation state +3, but other oxidation states are known especially in the solid state. Gadolinium(II) halides are obtained by heating Gd(III) halides in presence of metallic Gd in tantalum containers. Gadolinium also form sesquichloride Gd2Cl3, which can be further reduced to GdCl by annealing at 800 °C. This gadolinium(I) chloride forms platelets with layered graphite-like structure.[9]

[edit] Compounds

See also: Category:Gadolinium compounds

Compounds of gadolinium include

  • Fluorides: GdF3
  • Chlorides: GdCl3
  • Bromides: GdBr3
  • Nitrates: Gd(NO3)3
  • Iodides: GdI3
  • Oxides: Gd2O3
  • Sulfides: Gd2S3
  • Nitrides: GdN
  • Organics: gadodiamide

[edit] Isotopes

Main article: Isotopes of gadolinium

Naturally occurring gadolinium is composed of 6 stable isotopes, 154Gd, 155Gd, 156Gd, 157Gd, 158Gd and 160Gd, and 1 radioisotope, 152Gd, with 158Gd being the most abundant (24.84% natural abundance). The predicted double beta decay of 160Gd has never been observed (the only lower limit on its half-life of more than 1.3×1021 years has been set experimentally [10]).

Twenty-nine radioisotopes have been characterized, with the most stable being alpha-decaying 152Gd (naturally occurring) with a half-life of 1.08×1014 years, and 150Gd with a half-life of 1.79×106 years. All of the remaining radioactive isotopes have half-lives of less than 74.7 years. The majority of these have half-lives of less than 24.6 seconds. Gadolinium isotopes have 4 metastable isomers, with the most stable being 143mGd (T½=110 seconds), 145mGd (T½=85 seconds) and 141mGd (T½=24.5 seconds).

Isotopes with atomic masses lower than the most abundant stable isotope, 158Gd, primarily decay via electron capture to Eu (europium) isotopes. At higher atomic masses, the primary decay mode is beta decay, and the primary products are Tb (terbium) isotopes.

[edit] History

In 1880, Swiss chemist Jean Charles Galissard de Marignac observed spectroscopic lines due to gadolinium in samples of didymium and gadolinite; French chemist Paul Émile Lecoq de Boisbaudran separated gadolinia, the oxide of gadolinium, from Mosander's yttria in 1886. The element itself was isolated only recently. Gadolinium, like the mineral gadolinite, is named after Finnish chemist and geologist Johan Gadolin.[2]

[edit] Occurrence

Gadolinite

Gadolinium is a constituent in many minerals such as monazite and bastnäsite, which are oxides. The metal is too reactive to exist naturally. Ironically, the mineral gadolinite contains only traces of Gd. The abundance in the earth crust is about 6.2 mg/kg.[2] The main mining areas are China, USA, Brazil, Sri Lanka, India and Australia with reserves expected to exceed one million tonnes. World production of pure gadolinium is about 400 tonnes per year.

[edit] Production

Gadolinium is produced both from monazite and bastnäsite.

  1. Crushed minerals are extracted with hydrochloric or sulfuric acids, which converts the insoluble oxides into soluble chlorides or sulfates.
  2. The acidic filtrates are partially neutralized with caustic soda to pH 3–4. Thorium precipitates as its hydroxide and is removed.
  3. The remaining solution is treated with ammonium oxalate to convert rare earths in to their insoluble oxalates. The oxalates are converted to oxides by heating.
  4. The oxides are dissolved in nitric acid that excludes one of the main components, cerium, whose oxide is insoluble in HNO3.
  5. The solution is treated with magnesium nitrate to produce a crystallized mixture of double salts of gadolinium, samarium and europium.
  6. The salts are separated by ion exchange chromatography.
  7. The rare earth ions are then selectively washed out by suitable complexing agent.[2]

Gadolinium metal is obtained from its oxide or salts by heating with calcium at 1450 °C under argon atmosphere. Sponge gadolinium can be produced by reducing molten GdCl3 with an appropriate metal at temperatures below 1312 °C (melting point of Gd) in a reduced pressure.[2]

[edit] Applications

Gadolinium has no large-scale applications but has a variety of specialized uses.

With the highest neutron cross-section among any stable nuclides, 61,000 barns for 155Gd and 259,000 barns for 157Gd. 157Gd has been used to target tumors in neutron therapy. This element is very effective for use with neutron radiography and in shielding of nuclear reactors. It is used as a secondary, emergency shut-down measure in some nuclear reactors, particularly of the CANDU type.[2] Gadolinium is also used in nuclear marine propulsion systems as a burnable poison.

Gadolinium also possesses unusual metallurgic properties, with as little as 1% of gadolinium improving the workability and resistance of iron, chromium, and related alloys to high temperatures and oxidation.

Gadolinium is paramagnetic at room temperature, with a ferromagnetic Curie point of 17 °C.[11] Paramagnetic ions, such as gadolinium, move differently within a magnetic field. This trait makes gadolinium useful for magnetic resonance imaging (MRI). Solutions of organic gadolinium complexes and gadolinium compounds are used as intravenous MRI contrast agent to enhance images in medical magnetic resonance imaging and magnetic resonance angiography (MRA) procedures. Magnevist is the most widespread example.[12][13] Nanotubes packed with gadolinium, dubbed "gadonanotubes," are 40 times more effective than this traditional gadolinium contrast agent.[14] Once injected, gadolinium-based contrast agents accumulate in abnormal tissues of the brain and body. This accumulation provides a greater contrast between normal and abnormal tissues, allowing doctors to better locate uncommon cell growths and tumors.

Gadolinium-153 helps calibrate positron emission tomography (PET) systems that are used in nuclear medicine for functional imaging. This PET image of the human brain shows the difference between a normal brain and the clinically depressed patient. The blue color indicates less glucose metabolism in a normal brain. The green, yellow, and red colors indicate areas of higher glucose metabolism characteristic of a depressed patient.[15]

Gadolinium is also used in other imaging besides MRIs. In X-ray systems, gadolinium is contained in the phosphor layer, suspended in a polymer matrix at the detector. Terbium-doped gadolinium oxysulfide (Gd2O2S: Tb) at the phosphor layer converts the X-rays released from the source into light. This material emits green light at 540 nm due to the presence of Tb3+, which is very useful for enhancing the imaging quality. The energy conversion of Gd is up to 20%, which means that one-fifth of the X-rays striking the phosphor layer can be converted into light photons. Gadolinium oxyorthosilicate (Gd2SiO5, GSO; usually doped by 0.1–1% of Ce) is a single crystal that is used as a scintillator in medical imaging such as positron emission tomography or for detecting neutrons.[16]

Gadolinium-153 is produced in a nuclear reactor from elemental europium or enriched gadolinium targets. It has a half-life of 240±10 days and emits gamma radiation with strong peaks at 41 keV and 102 keV. It is used in many quality assurance applications, such as line sources and calibration phantoms, to ensure that nuclear medicine imaging systems operate correctly and produce useful images of radioisotope distribution inside the patient.[15] It is also used as a gamma ray source in X-ray absorption measurements or in bone density gauges for osteoporosis screening, as well as in the Lixiscope portable X-ray imaging system.[17]

Gadolinium is used for making gadolinium yttrium garnet (Gd:Y3Al5O12); it has microwave applications and is used in fabrication of various optical components and as substrate material for magneto–optical films.

Gadolinium compounds are also used for making green phosphors for colour TV tubes and compact discs.

Gadolinium Gallium Garnet (GGG, Gd3Ga5O12) was used for imitation diamonds and for computer bubble memory.[18]

[edit] Biological role

Gadolinium has no known native biological role, but its compounds are used as research tools in biomedicine. Gd3+ compounds are components of MRI contrast agents. It is used in various ion channel electrophysiology experiments to block sodium leak channels, as well as to stretch activated ion channels.[19]

[edit] Safety

As a free ion, gadolinium is highly toxic, but MRI contrast agents are chelated compounds and are considered safe. The toxicity depends on the strength of the chelating agent.[20] US Food and Drug Administration approved Gd chelated contrast agents include: Omniscan, Multihance, Magnevist, ProHance, Vasovist, Eovist and OptiMARK.[21]

Gadolinium MRI contrast agents have proved safer than the iodinated contrast agents used in X-ray radiography or computed tomography. Anaphylactoid reactions are rare, occurring in approx. 0.03–0.1%.[22]

Although gadolinium agents have proved useful for patients with renal impairment, in patients with severe renal failure requiring dialysis there is a risk of a rare but serious illnesses, such as nephrogenic systemic fibrosis[23] and nephrogenic fibrosing dermopathy,[24] that may be linked to the use of certain gadolinium-containing agents. Current guidelines in the United States are that dialysis patients should only receive gadolinium agents where essential, and that dialysis should be performed as soon as possible after the scan is complete, in order to remove the agent from the body promptly.[25] However, after several years of controversy during which up to 100 Danish patients have been gadolinium poisoned (and some died) after Omniscan use, it has been admitted by the Norwegian medical company Nycomed that they were aware of the dangers of using gadolinium based agents for their product.

引用出處:

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

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 инструментыПустотелое 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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(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.