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Lutetium 2-

There are few applications for lutetium. The supply is Hmited and the price high. If the Lu atom is activated by thermal neutrons its nucleus emits a pure P-radiation. In this form the metal can be used as a catalyst for cracking and polymerization. [Pg.490]

Stability constants for LuOH have been reported in a number of studies and are listed in Table 8.52. The majority of the available data have been measured in a NaClO medium. Two of the studies calculated a value for the stability constant at zero ionic strength and the values obtained are in very good agreement (see Table 8.52). All of the data listed in the table (except for the value from Wheelwright, Spedding and Schwarzenbach (1953)) are retained in the present review. [Pg.303]

25 0 — Data at fixed ionic strength 0 -7.32 -7.32 0.20 Usherenko and Skorik (1972)  [Pg.304]

Fatin-Rouge and Biinzli (1999) is the only study to give stability constant data for the higher monomeric species of lutetium. The conclusion reached with the other lanthanides is also appropriate for lutetium that is, the data are not consistent [Pg.304]

The thermodynamic data for the standard state (elemental solids) and trivalent ions of the lanthanide metals are taken from Bard, Parsons and Jordan (1985). The enthalpy of formation for some of the trivalent ions is taken from Merli, Rorif and Fuger (1998). The data are listed in Table 8.53. They have been utilised in deriving the thermodynamic data Usted in Table 8.17. [Pg.305]


Liu Y, Shigehara K and Yamada A 1989 Purification of lutetium diphthalocyanine and electrochromism of its Langmuir-Blodgett films Thin Soiid Fiims 179 303-8... [Pg.2633]

Reference has been made already to the existence of a set of inner transition elements, following lanthanum, in which the quantum level being filled is neither the outer quantum level nor the penultimate level, but the next inner. These elements, together with yttrium (a transition metal), were called the rare earths , since they occurred in uncommon mixtures of what were believed to be earths or oxides. With the recognition of their special structure, the elements from lanthanum to lutetium were re-named the lanthanons or lanthanides. They resemble one another very closely, so much so that their separation presented a major problem, since all their compounds are very much alike. They exhibit oxidation state -i-3 and show in this state predominantly ionic characteristics—the ions. [Pg.441]

Ytterby, village in Sweden) Marignac in 1878 discovered a new component, which he called ytterbia, in the earth then known as erbia. In 1907, Urbain separated ytterbia into two components, which he called neoytterbia and lutecia. The elements in these earths are now known as ytterbium and lutetium, respectively. These elements are identical with aldebaranium and cassiopeium, discovered independently and at about the same time by von Welsbach. [Pg.196]

Lanthanides is the name given collectively to the fifteen elements, also called the elements, ranging from lanthanum. La, atomic number 57, to lutetium, Lu, atomic number 71. The rare earths comprise lanthanides, yttrium, Y, atomic number 39, and scandium. Sc, atomic number 21. The most abundant member of the rare earths is cerium, Ce, atomic number 58 (see Ceriumand cerium compounds). [Pg.539]

Parameter Gadolinium Terbium Dysprosium Holmium Erbium ThuUmn Ytterbium Lutetium... [Pg.541]

Separation Processes. The product of ore digestion contains the rare earths in the same ratio as that in which they were originally present in the ore, with few exceptions, because of the similarity in chemical properties. The various processes for separating individual rare earth from naturally occurring rare-earth mixtures essentially utilize small differences in acidity resulting from the decrease in ionic radius from lanthanum to lutetium. The acidity differences influence the solubiUties of salts, the hydrolysis of cations, and the formation of complex species so as to allow separation by fractional crystallization, fractional precipitation, ion exchange, and solvent extraction. In addition, the existence of tetravalent and divalent species for cerium and europium, respectively, is useful because the chemical behavior of these ions is markedly different from that of the trivalent species. [Pg.543]

Some nut trees accumulate mineral elements. Hickory nut is notable as an accumulator of aluminum compounds (30) the ash of its leaves contains up to 37.5% of AI2O2, compared with only 0.032% of aluminum oxide in the ash of the Fnglish walnut s autumn leaves. As an accumulator of rare-earth elements, hickory greatly exceeds all other plants their leaves show up to 2296 ppm of rare earths (scandium, yttrium, lanthanum, dysprosium, holmium, erbium, thulium, ytterbium, and lutetium). The amounts of rare-earth elements found in parts of the hickory nut are kernels, at 5 ppm shells, at 7 ppm and shucks, at 17 ppm. The kernel of the Bra2d nut contains large amounts of barium in an insoluble form when the nut is eaten, barium dissolves in the hydrochloric acid of the stomach. [Pg.272]

The same color variety is not typical with inorganic insertion/extraction materials blue is a common transmitted color. However, rare-earth diphthalocyanine complexes have been discussed, and these exhibit a wide variety of colors as a function of potential (73—75). Lutetium diphthalocyanine [12369-74-3] has been studied the most. It is an ion-insertion/extraction material that does not fit into any one of the groups herein but has been classed with the organics in reviews. Films of this complex, and also erbium diphthalocyanine [11060-87-0] have been prepared successfiiUy by vacuum sublimation and even embodied in soHd-state cells (76,77). [Pg.158]

To avoid this confusion, and because many of the elements are actually far from rare, the terms lanthanide , lanthanon and lanthanoid have been introduced. Even now, however, there is no general agreement about the position of La, i.e, whether the group is made up of the elements La to Lu or Ce to Lu. Throughout this chapter the term lanthanide and the general symbol, Ln, will be used to refer to the fourteen elements cerium to lutetium inclusive, the Group 3 elements, scandium, yttrium and lanthanum having already been dealt with in Chapter 20. [Pg.1227]

The lanthanides comprise the largest naturally-occurring group in the periodic table. Their properties are so similar that from 1794, when J. Gadolin isolated yttria which he thought was the oxide of a single new element, until 1907, when lutetium was discovered, nearly a hundred claims were made for the discovery of elements... [Pg.1227]

Dysprosium, Dy Lutetium, Lu > L. de Boisbaudran G. Urbain 1886 Greek hvanpoaixog, dysprositos, hard to get... [Pg.1229]


See other pages where Lutetium 2- is mentioned: [Pg.45]    [Pg.235]    [Pg.242]    [Pg.243]    [Pg.9]    [Pg.440]    [Pg.440]    [Pg.440]    [Pg.198]    [Pg.198]    [Pg.198]    [Pg.217]    [Pg.248]    [Pg.273]    [Pg.278]    [Pg.323]    [Pg.349]    [Pg.631]    [Pg.663]    [Pg.720]    [Pg.838]    [Pg.848]    [Pg.912]    [Pg.957]    [Pg.1185]    [Pg.351]    [Pg.580]    [Pg.580]    [Pg.580]    [Pg.245]    [Pg.217]    [Pg.217]    [Pg.539]    [Pg.540]    [Pg.540]    [Pg.540]    [Pg.542]    [Pg.306]    [Pg.51]   
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Catalysts containing lutetium

Catalysts lutetium

Cerium doped lutetium

Cerium metals lutetium neodymium

Cesium lutetium chloride

Cesium lutetium chloride (Cs2LuC

Determination lutetium

Dysprosium metals lutetium neodymium

Erbium metals lutetium neodymium

Europium metals lutetium neodymium

Furan, tetrahydro-, lanthanide complexes lutetium complex

Gadolinium metals lutetium neodymium

High pressure lutetium

Lanthanides lutetium

Lu LUTETIUM

Lutetium 218 Subject

Lutetium abundance

Lutetium adduct

Lutetium alloys

Lutetium alloys with

Lutetium analog

Lutetium atomic radius

Lutetium atomization enthalpy

Lutetium bis

Lutetium carbonates

Lutetium chloride

Lutetium chloride (LuCl

Lutetium chloro

Lutetium complexes

Lutetium complexes 1,3-diketones

Lutetium complexes hydrolysis

Lutetium compounds

Lutetium compounds/complexes, coordination

Lutetium compounds/complexes, coordination numbers

Lutetium coordination number

Lutetium diphthalocyanine

Lutetium discovery

Lutetium earths

Lutetium electrical resistivity

Lutetium electron configuration

Lutetium electronic configuration

Lutetium element

Lutetium europium gadolinium holmium

Lutetium fluoride

Lutetium ground state electronic configuration

Lutetium half-life

Lutetium halides

Lutetium hardness

Lutetium heat capacity

Lutetium history, occurrence, uses

Lutetium hydrates

Lutetium hydration

Lutetium hydride

Lutetium initiators

Lutetium intensities

Lutetium ion

Lutetium ionic complexes

Lutetium ionization

Lutetium ionization energies

Lutetium isopropoxide

Lutetium isotope

Lutetium isotopes and their properties

Lutetium lanthanide metals neodymium

Lutetium metal

Lutetium molten, density

Lutetium nitrates

Lutetium organometallic compounds

Lutetium oxidation states

Lutetium oxide

Lutetium oxyorthosilicate

Lutetium phthalocyanine

Lutetium physical properties

Lutetium porphyrins

Lutetium praseodymium samarium

Lutetium pressure

Lutetium radioisotope

Lutetium radionuclides

Lutetium sandwich complexes

Lutetium selenides

Lutetium selenites

Lutetium spectra

Lutetium structure

Lutetium superconducting

Lutetium susceptibility

Lutetium telluride

Lutetium tetra

Lutetium texaphyrin

Lutetium thermal properties

Lutetium triflate

Lutetium trinitrato

Lutetium vapor pressure

Lutetium vapor pressure, high temperature

Lutetium, phthalocyanine ligands

Lutetium, porphyrin complexes

Lutetium, properties

Lutetium, purification of, from

Lutetium, purification of, from Lu Yb acetate solution

Lutetium, role

Lutetium-isobutyl complex

Lutetium-methyl complexes

Motexafin lutetium

Praseodymium gadolinium holmium lutetium

Rare earth metals Lutetium Neodymium Praseodymium

Samarium lanthanide metals lutetium

Silane tetramethyl-, lutetium complex

Superconductivity lutetium

With lutetium

Ytterbium and Lutetium

Ytterbium lanthanide metals lutetium

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