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Lanthanum oxide chlorides

Another method involves heating lanthanum oxide with excess ammonium chloride at 300°C ... [Pg.447]

The first metallofullerenes, La C2 , were discovered by Smalley et al.18,23 after laser vaporization of composite targets made of graphite and lanthanum oxide or chloride. Because of their low-yield synthesis, laborious purification, and often air sensitivity and kinetic instability, studying the physical properties and chemical reactivity of these fascinating compounds was a serious challenge. Fortunately, the high sensitivity of the electrochemical methods was well adapted to study the microgram quantities in which these materials were usually available. The series of M C82... [Pg.205]

Chemicae Eormulas Common compounds o Cerium oxide CeiOs o Gadolinium oxide Gd203 o Lanthanum oxide LaiOs o Yttrium oxide Y2O3 o Cerium nitrate Ce(N03)3 o Cerium chloride CeCls... [Pg.1502]

The lanthanum(III) oxide chlorides might all be expected to react similarly with phosgene ... [Pg.363]

The reaction of lanthanum(III) oxide fluoride, a-LaOF, with phosgene has been investigated as a function of time and temperature (430, 500 and 680 C) by t.g.a., followed by product analysis and characterization by powder X-ray diffraction [113]. This is a much more thorough study than those described above for the lanthanide oxide chlorides, and the results are summarized in Fig. 9.9. All the fluoride ends up as LaF (thus no significant quantities of COCIF or COFj can be formed), and the major product at each temperature is LaOCl. The product analysis is consistent with the following sequential reactions occurring [113] ... [Pg.364]

According to Ten et al. [15] the most used nucleating agents for PHBV polymers are boron nitride, talc, lanthanum oxide, saccharin, phthalimide, thymine and melamine, ammonium chloride, and NCC. [Pg.264]

The determination of magnesium in potable water is very straightforward very few interferences are encountered when using an acetylene-air flame. The determination of calcium is however more complicated many chemical interferences are encountered in the acetylene-air flame and the use of releasing agents such as strontium chloride, lanthanum chloride, or EDTA is necessary. Using the hotter acetylene-nitrous oxide flame the only significant interference arises from the ionisation of calcium, and under these conditions an ionisation buffer such as potassium chloride is added to the test solutions. [Pg.804]

The superconducting oxides include both perovskites and Ruddlesden-Popper compounds which have an orthorhombic arrangement of cubic cells, alternatively of the perovskite and sodium chloride structures. The common feature of all of these is the presence of copper as a major component. The first ceramic superconductor was a lanthanum-strontium substituted cuprate (Lai Sr Cu04 z), which is a perovskite, but subsequently the inter-oxide compound Y203 2BaO 3CuO, commonly referred to as a 123 compound, was shown to have superior performance. The speculation concerning the conduction mechanism is that this involves either Cu3+-Cu2+ positive hole... [Pg.247]

The metallothermic reduction of the oxides by La produces the metals Sm, Eu, Tm, Yb, all having high vapour pressures. The reaction goes to completion due to the removal of the rare earths by volatilization from the reaction chamber (lanthanum has a low vapour pressure). The remaining rare earth metals (Sc, La, Ce, Pr, Nd, Y, Gd, Tb, Dy, Ho, Er, Lu) can be obtained by quantitative conversion of the oxides in fluorides, followed by reduction with Ca. The metallothermic reduction of the anhydrous rare earth chlorides could be also used to obtain La, Ce, Pr and Nd. The molten electrolysis can be applied to obtain only the first four lanthanide metals, La, Ce, Pr and Nd, because of the high reactivity of the materials that limits the operating temperatures to 1100°C or lower. [Pg.362]

Lanthanum in purified metallic state may be obtained from its purified oxide or other salts. One such process involves heating the oxide with ammonium chloride or ammonium fluoride and hydrofluoric acid at 300° to 400° C in a tantalum or tungsten crucible. This is followed by reduction with alkali or alkaline earth metals at 1,000°C under argon or in vacuum. [Pg.446]

When lanthanum is produced from the mineral bastnasite, all processes except ore extraction discussed above are the same. The mineral is crushed and concentrated by flotation process. This is followed by treatment with dilute HCl, which converts lanthanum and the rare-earths contained in the mineral into their chlorides. Calcination in air results in rare-earth oxides. [Pg.446]

Heating the oxide with an excess of ammonium chloride yields lanthanum chloride ... [Pg.452]

Many metal chlorides when heated with an excess of nitric acid are converted into the nitrates. Thus, J. L. Smith found that the transformation occurs with potassium or sodium chloride in the presence of 7 to 8 parts of nitric acid J. S. Stas said that at 40°-50°, potassium, sodium, or lithium chloride require respectively 3, 4, and 5-5 parts of nitric acid. J. L. Smith said that ammonium chloride and nitric acid yield nitrous oxide. H. Wurtz found that auric, cadmium, cerium, lanthanum, didymium, ferric, and platinic chlorides are decomposed by nitric acid incompletely and with difficulty. S. Schlesinger said that the two copper chlorides, mercurous, zinc, and lead chlorides, are decomposed, but, added H. Wurtz, with difficulty and incompletely while mercuric ajid silver chlorides are not attacked. F. Rose found cobalt amminochlorides are readily converted into the nitrate. [Pg.595]

Lanthanum nitrate, analysis of anhydrous, 5 41 Lead (IV) acetate, 1 47 Lead(II) 0,0 -diethyl dithiophos-phate, 6 142 Lead (IV) oxide, 1 45 Lead(II) thiocyanate, 1 85 Lithium amide, 2 135 Lithium carbonate, formation of, from lithium hydroperoxide 1-hydrate, 5 3 purification of, 1 1 Lithium chloride, anhydrous, 6 154 Lithium hydroperoxide 1-hydrate, 5 1... [Pg.239]

Praseodymium, separation of mixtures with lanthanum from monazite, as magnesium nitrate double salt, 2 56, 67 Praseodymium (III) nitrate, analysis of anhydrous, 5 41 Praseodymium (III) oxide, for synthesis of nitrate, 5 39w. Precipitates, apparatus for removing liquid from, 8 16 Purpureochromic chloride, 2 196 6 138... [Pg.245]


See other pages where Lanthanum oxide chlorides is mentioned: [Pg.121]    [Pg.133]    [Pg.419]    [Pg.219]    [Pg.133]    [Pg.135]    [Pg.1503]    [Pg.1910]    [Pg.50]    [Pg.42]    [Pg.137]    [Pg.163]    [Pg.112]    [Pg.56]    [Pg.366]    [Pg.53]    [Pg.247]    [Pg.944]    [Pg.295]    [Pg.98]    [Pg.105]    [Pg.215]    [Pg.200]    [Pg.137]    [Pg.115]    [Pg.201]    [Pg.157]    [Pg.199]    [Pg.397]    [Pg.419]    [Pg.186]   
See also in sourсe #XX -- [ Pg.363 ]




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Oxidation chloride

Oxide chlorides

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