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Yttrium

Y • Atomic Number 39

Yttrium

Yttrium is a silvery, relatively soft, and reactive metal that belongs to the transition metals. Although chemically it is not part of the lanthanide group, yttrium is classified as a heavy rare earth element. In the Earth's crust, yttrium is the fourth most abundant element among the rare earth elements.

Chemically, however, it behaves very similarly to the heavy lanthanides (especially dysprosium and holmium). Therefore, yttrium tends to associate with the heavy rare earth elements in mineral deposits.

Yttrium is superconducting, phosphorescent, and very strong.

Its most important application is as a phosphor in display screens.

Yttrium (named after Ytterby, a mine near the Swedish capital Stockholm) was discovered in 1794 by Johan Gadolin in the mineral ytterbite. In 1824, Friedrich Wöhler produced impure yttrium by reducing yttrium chloride with potassium. It was not until 1842 that Carl Gustav Mosander successfully separated yttrium from the accompanying elements erbium and terbium.

It is named after its first discovery site, the Ytterby mine near Stockholm, along with ytterbium, terbium, and erbium.

  • Occurence

    The mineral xenotime is the most important source for yttrium extraction.

    Australia dominates global xenotime production. The country possesses the largest and most economically viable heavy mineral sand deposits in the world.

  • Extraction

    The metal is produced by electrolysis and metallothermic reduction of its halides using alkali or alkaline earth metals. It exists in four allotropes (structural forms). The α-phase is face-centered cubic with a lattice parameter of a = 4,85 Å at 77 K (-196 °C or -321 °F). The β-phase forms just below room temperature and is hexagonal close-packed with a = 3.6810 Å and c = 11.857 Å. The γ-phase is the room temperature form and is face-centered cubic with a = 5.1610 Å at 24 °C (75 °F). The δ-phase is body-centered cubic with a = 4,12 Å at 757 °C (1.395 °F).

    After an elaborate separation of cerium impurities, the oxide is converted to cerium fluoride using hydrofluoric acid. It is then reduced with calcium, forming calcium fluoride in the process. The removal of residual calcium and impurities is achieved through an additional vacuum remelting step.

  • Application

    The most important application of yttrium is as a phosphor in displays. Europium-doped yttrium oxysulfide (Y₂O₂S:Eu³⁺) produces the perfect, intense red color in the cathode ray tubes (CRTs) of old color televisions and computer monitors. In modern white LEDs, a blue LED is often combined with a yttrium-aluminum garnet (YAG) phosphor that emits yellow light. The combination of blue and yellow light appears white to the human eye.

    Yttrium is also used as a crystal in high-performance lasers for medical applications, material processing (welding, engraving), metrology, and defense.

    Yttrium oxide is additionally used in superalloys to improve high-temperature and corrosion resistance.

Yttrium, Y, atomic number 39, transition metal, rare earth metal, heavy rare earth, phosphors, display technology, high-tech applications, superconductors, electronic materials, mineral xenotime, ISE AG metals, ISE AG

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Ytterbium

Yb • Atomic Number 70

Ytterbium

Ytterbium is a soft, silvery-white, malleable metal with unique optical and electronic properties. It belongs to the heavy rare earth elements.

Ytterbium ions have well-defined absorption and emission bands in the near-infrared region (around 980 nm excitation and 1030 nm emission). This property forms the basis for its most important application in ytterbium-doped lasers used in fiber optic networks.

Ytterbium stands out from other elements because it is stable in both the +3 and +2 oxidation states. This “divalency” enables unique chemical reactions.

Another notable property is that ytterbium compounds are often paramagnetic (attracted by magnetic fields). This makes it useful in alloys where magnetic interference is undesirable.

Ytterbium was discovered in 1878 by the Swiss chemist Jean Charles Galissard de Marignac. He studied gadolinite more closely and identified a previously unknown element, which he named ytterbium after the Swedish locality Ytterby, where the gadolinite was found, and due to its similarity to yttrium.

  • Occurence

    The main sources for ytterbium extraction are bastnäsite and monazite deposits. These are primarily mined in China, with smaller-scale mining also occurring in the USA, Australia, and Southeast Asia.

    The demand for ytterbium is growing due to its use in a variety of technologies.

    Ytterbium production is almost exclusively concentrated in China.

  • Extraction

    Ytterbium is obtained through solvent extraction. For this process, the rare earth oxide (REO) mixture is dissolved in hydrochloric acid, and the solution is pumped through a series of mixer-settler units. At each stage, an organic solvent is added that selectively binds a specific rare earth element.

    Due to slight differences in the acidity of the ions, the various elements move through the cascade at different rates.

    Ytterbium accumulates in the later stages of the extraction cascade.

    The result of this step is highly pure ytterbium(III) oxide (Yb₂O₃).

    To produce metallic ytterbium, the oxide is usually reduced metallothermically using lanthanum or cerium.

    The metal obtained by reduction is often not pure enough for high-tech applications. The most important purification method is in-situ distillation.

  • Application

    One of the key drivers for ytterbium demand is the expansion of fiber optic networks and 5G. Ytterbium plays a crucial role in high-performance semiconductors and ytterbium-doped fiber amplifiers (YDFAs). Ytterbium-based amplifiers, an essential component in fiber lasers, enable efficient high-speed data transmission in communication technologies.

    Another important application of ytterbium is in medical technologies. Ytterbium isotopes are used in medical imaging, radiation therapy, and surgical lasers.

    Ytterbium demand could further increase in the future due to innovations in emerging fields such as quantum computing and ultra-precise atomic clocks.

    General Information
    Name, Symbol, Atomic Number Ytterbium, Yb, 70
    Series Lanthanoid
    Groupe, Periode, Block La, 6, f
    Appearance silvery-white
    CAS-Number 7440-64-4
    Abundance in Earth's crust 2.5ppm
    Atomic Properties
    Atomic Mass 173.04 u
    Atomic Radius 175 pm
    Covalent Radius 187 pm
    Electron Configuration [Xe] 4f¹⁴ 6s²
    1. Ionization Energy 603.4 kJ/mol
    2. Ionization Energy 1174.8 kJ/mol
    3. Ionization Energy 2417 kJ/mol
    4. Ionization Energy -
    Physical Properties
    State of Matter solid
    Crystal Structure Cubic face-centered
    Density 6.973 g/cm³ (at 25 °C)
    Magnetism

    Paramagnetic (χm = 3.4 * 10⁻⁵)

    Melting Point 1097 K (824 °C)
    Boiling Point 1469 K (1196 °C)
    Molar Volume 24.84 * 10⁻⁶ m³/mol
    Heat of Vaporization 160 kJ/mol
    Heat of Fusion 7.7 kJ/mol
    Electrical Conductivity 4.0 * 10⁶ A/(V·m)
    Thermal Conductivity 39 W/(m*K)

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Thulium

Tm • Atomic Number 69

Thulium

Thulium is a silvery-gray metal that is very soft, ductile, and malleable. It belongs to the heavy rare earth elements.

It is highly reactive and has a high melting point (1545 °C). The naturally occurring isotope thulium-169 is stable, making it suitable for many applications.

The most important commercial use of thulium is in portable X-ray devices.

Thulium is named after Thule, the mythical island at the edge of the world, and was discovered in 1879 by the Swedish chemist Per Teodor Cleve, along with holmium, in erbia (erbium oxide).

  • Occurence

    Thulium is the rarest of the naturally occurring lanthanides and the second rarest among the rare earth metals, making it correspondingly expensive. Its abundance in the Earth's crust is estimated at about 0,5 ppm.

    The main host minerals for thulium are monazite and xenotime.

    Xenotime, which is particularly rich in heavy rare earth elements, contains a somewhat higher concentration of thulium than bastnäsite and monazite.

  • Extraction

    Thulium is obtained through solvent extraction. For this process, the rare earth oxide (REO) mixture is dissolved in hydrochloric acid, and the solution is pumped through a series of mixer-settler units. At each stage, an organic solvent is added that selectively binds a specific rare earth element.

    Due to slight differences in the acidity of the ions, the various elements move through the cascade at different rates.

    Thulium, being one of the heavier lanthanides, accumulates in the later stages of the extraction cascade.

    The result of this step is highly pure thulium(III) oxide (Tm₂O₃), also known as “thulia.”

    To obtain metallic thulium, the oxide is usually reduced metallothermically using lanthanum or cerium.

    The metal produced by reduction is often not pure enough for high-tech applications. The most important purification method is vacuum distillation.

  • Application

    Compared to other rare earth elements, the demand for thulium is limited and its applications are confined to niche areas.

    The most important use of thulium is in portable X-ray devices. When thulium-169 is irradiated, it produces thulium-170. This isotope serves as a highly efficient, portable, and safe source of soft gamma radiation, similar to that used in X-ray equipment. Since these radiation sources require no external power supply or complex cooling, they are ideal for portable X-ray devices used in non-destructive testing (e.g., weld inspection) at hard-to-reach locations such as pipelines or construction sites, as well as for medical applications in remote areas without electricity.

    Another application of thulium is in high-power lasers. Thulium-doped solid-state lasers (e.g., using YAG or YLF crystals), employed in medical surgery and LIDAR (Light Detection and Ranging) systems, are extremely powerful and efficient.

    Thulium is also used as a dopant in specialized phosphors and has niche applications in materials research.

    Furthermore, thulium’s excellent performance in high-temperature superconductors makes it indispensable for the development of advanced electronic devices. It contributes to the production of highly efficient lasers, especially those operating in the infrared spectrum, which are crucial for precision surgical instruments and industrial applications.

    General Information

    Name, Symbol, Atomic Number Thulium, Tm, 69
    Series Lanthanoid
    Group, Period, Block La, 6, f
    Appearance Silvery gray
    CAS-Number 7440-30-4
    Abundance in Earth's crust 0.19 ppm
    Atomic Properties
    Atomic Mass 168.93421 u
    Atomic Radius 175 pm
    Covalent Radius 190 pm
    Electron configuration [Xe] 4f¹³ 6s²
    1. Ionization Energy 596.7 kJ/mol
    2. Ionization Energy 1160 kJ/mol
    3. Ionization Energy 2285 kJ/mol
    4. Ionization Energy -
    Physical Properties
    State of Matter solid
    Crystal Structure Hexagonal
    Density 9.318 g/cm³ (at 25 °C)
    Magnetism

    Paramagnetic (χm = 0.017)

    Melting Point 1818 K (1545 °C)
    Boiling Point 2223 K (1950 °C)
    Molar Volume 19.1 * 10⁻⁶ m³/mol
    Heat of Vaporization 250 kJ/mol
    Heat of Fusion 16.8 kJ/mol
    Electrical Conductivity 1.477 * 10⁶ A/(V·m)
    Thermal Conductivity 16.8 W/(m*K)

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Terbium

Tb • Atomic Number 65

Terbium

Terbium is a silvery, soft metal that belongs to the heavy rare earth elements.

Its special properties are its uniquely efficient green luminescence and extremely strong magnetostriction. These characteristics make terbium a critical and irreplaceable raw material for high-tech applications.

The discovery of terbium is as complex and unclear as that of other rare earth elements.

Carl Gustav Mosander is generally credited as the discoverer. In the early 1840s, he studied the “yttria” discovered by Johan Gadolin. However, the supposedly pure terbium compound was actually a mixture of several lanthanides. Pure terbium was only produced after 1945 with the advent of ion-exchange techniques. Mosander derived the element’s name from the Swedish mine Ytterby.

  • Occurence

    Xenotime is one of the most important sources of heavy rare earth elements. It contains significant amounts of terbium, dysprosium, and erbium.

    Ion-adsorption clays are another economically important source.

    China controls the mining and production of terbium and other heavy rare earth elements.

  • Extraction

    After a complex separation of other terbium-associated elements, the oxide is converted to terbium fluoride using hydrofluoric acid. It is then reduced to metallic terbium with calcium, producing calcium fluoride as a by-product. Any remaining calcium residues and impurities are removed in an additional vacuum remelting process.

     

  • Application

    Die wichtigste Anwendung von Terbium ist seine Verwendung als Aktivator für grüne Lumineszenz in Leuchtstoffen. Diese eine Anwendung ist für den Großteil der Nachfrage verantwortlich. Terbium-basierte Leuchtstoffe sind aufgrund ihrer extrem effizienten und hellen grünen Lichtemission in vielen Schlüsseltechnologien unersetzlich.

    Terbium wird daher in einer Vielzahl von Beleuchtungs- und Displaytechnologien genutzt. Dazu zählen weiße LEDs, Flachbildschirme (OLEDs & Plasmadisplays), Leuchtstofflampen (Energiesparlampen).

    Die zweite äußerst wichtige Anwendung ist in der Legierung Terfenol-D (eine Legierung aus Terbium, Eisen und Dysprosium). Diese Legierung zeigt den stärksten bekannten magnetostriktiven Effekt: Dieser Effekt wird in Präzisions-Aktuatoren, Schallwandlern für Sonarsysteme (Marine), Schwingungskontrollsystemen und Sensoren genutzt.

    The most important application of terbium is its use as an activator for green luminescence in phosphors. This single application accounts for the majority of demand. Terbium-based phosphors are indispensable in many key technologies due to their extremely efficient and bright green light emission.

    Terbium is therefore used in a wide range of lighting and display technologies, including white LEDs, flat-panel displays (OLEDs and plasma displays), and fluorescent lamps (energy-saving lamps).

    The second highly important application is in the alloy Terfenol-D (an alloy of terbium, iron, and dysprosium). This alloy exhibits the strongest known magnetostrictive effect, which is utilized in precision actuators, sonar transducers (marine applications), vibration control systems, and sensors.

  • Unique Properties

    The silvery-gray rare earth metal terbium is ductile and malleable. Above 1315 °C, α-terbium (with an hcp crystal structure) transforms into β-terbium. Terbium is relatively stable in air, where it forms a protective oxide layer. When burned in a flame, it produces brown terbium(III,IV) oxide (Tb₄O₇). It reacts with water to form the hydroxide, releasing hydrogen gas.

     

     

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