Oxides rare earth

Another sol—gel abrasive, produced by seeding with a-ferric oxide or its precursors, has been patented (30). A magnesium-modified version of this abrasive, also called Cubitron, is being produced as a replacement for the earlier type. Yttria [1314-36-91-vnc>A V eA sol—gel abrasives have also been patented (31), as well as rare earth oxide modified materials (32). These abrasives are all produced by 3M Corporation they have performed very well ia various applications such as ia coated abrasives for grinding stainless steel and exotic alloys. 

The lanthanides, distributed widely in low concentrations throughout the earth s cmst (2), are found as mixtures in many massive rock formations, eg, basalts, granites, gneisses, shales, and siUcate rocks, where they are present in quantities of 10—300 ppm. Lanthanides also occur in some 160 discrete minerals, most of them rare, but in which the rare-earth (RE) content, expressed as oxide, can be as high as 60% rare-earth oxide (REO). Lanthanides do not occur in nature in the elemental state and do not occur in minerals as individual elements, but as mixtures. 

Table 6. Rare-Earth Oxide Distribution in Mineral and Clay Sources, wt ...

A large deposit of loparite occurs ia the Kola Peninsula, Russia. The production of REO reaches 6500 t/yr. Loparite contains over 30% of rare-earth oxides from the cerium group. In addition, loparite contains up to 40% titanium oxide and up to 12% niobium and tantalum oxides. 

Another characteristic of the solvent extraction system is the high solute concentration in both aqueous and organic phases, which influences greatly the size of the required installation. Concentrations of rare-earth oxides (REO) higher than 100 g/L are often reached in both phases. The process therefore requires only relatively small equipment. 

Re OPe . The final step in the chemical processing of rare earths depends on the intended use of the product. Rare-earth chlorides, usually electrolytically reduced to the metallic form for use in metallurgy, are obtained by crystallisation of aqueous chloride solutions. Rare-earth fluorides, used for electrolytic or metaHothermic reduction, are obtained by precipitation with hydrofluoric acid. Rare-earth oxides are obtained by firing hydroxides, carbonates or oxalates, first precipitated from the aqueous solution, at 900°C. 

SoHd lubricants ate added to help control high friction characteristics in high speed or heavy-duty appHcations where high temperatures are generated. Molybdenum disulfide [1317-33-5] M0S2, may be used alone or in a complex compound formed by grinding with fine natural graphite, and zinc sulfide [1314-98-3] ZnS. Other compounds include calcium fluoride, cryoHte [15096-52-3] Na AlF, rare-earth oxides, and metal sulfides, eg, iron, antimony, or zinc (see LUBRICATION AND LUBRICANTS). 

Other Rea.ctlons, The anhydride of neopentanoic acid, neopentanoyl anhydride [1538-75-6] can be made by the reaction of neopentanoic acid with acetic anhydride (25). The reaction of neopentanoic acid with acetone using various catalysts, such as titanium dioxide (26) or 2irconium oxide (27), gives 3,3-dimethyl-2-butanone [75-97-8] commonly referred to as pinacolone. Other routes to pinacolone include the reaction of pivaloyl chloride [3282-30-2] with Grignard reagents (28) and the condensation of neopentanoic acid with acetic acid using a rare-earth oxide catalyst (29). Amides of neopentanoic acid can be prepared direcdy from the acid, from the acid chloride, or from esters, using primary or secondary amines. 

Rare earth oxides and phosphors Ceramics (AI2O3) and glasses Mining ores and rocks Superconductors and precursor materials Thin films... 

Rare Earth. Increasing the amount of rare earth oxide (REO) on the zeolite decreases the octane (Figure 6-5). 

The examination and analysis of minerals have provided x-ray emission spectrography with a challenge and an opportunity. This situation has arisen because of a great growth of interest in uranium and thorium minerals in the rare-earth oxides and in metals such as tantalum and niobium, or hafnium and zirconium. On the whole, x-ray emission spectrography has met the challenge successfully, and the investigations that prove this also demonstrate the versatility and the value of the method.70"72... 

The relatively high cost and lack of domestic supply of noble metals has spurred considerable efforts toward the development of nonnoble metal catalysts for automobile exhaust control. A very large number of base metal oxides and mixtures of oxides have been considered, especially the transition metals, such as copper, chromium, nickel, manganese, cobalt vanadium, and iron. Particularly prominent are the copper chromites, which are mixtures of the oxides of copper and chromium, with various promoters added. These materials are active in the oxidation of CO and hydrocarbons, as well as in the reduction of NO in the presence of CO (55-59). Rare earth oxides, such as lanthanum cobaltate and lanthanum lead manganite with Perovskite structure, have been investigated for CO oxidation, but have not been tested and shown to be sufficiently active under realistic and demanding conditions (60-63). Hopcalities are out-... 

Storage are the fresh and 75 h aged Pd ly TWCs (Cl and C2), and it is likely that rare earth oxides do contribute to oxygen up es in those catalysts. Interestingly, the C1 and C2 catalysts are the only pair which show a correlation between oxygen uptake and noble metal dispersion (i-e. the oxygen titrated by the first CO pulse drops from 35.5 to 27.2 /i-mol O/g-cat. as the dispersion drops from 10.8% (Cl) to 3.5% (C2)). 

Dynamometer-aged (120 h) catalysts showed no evidence for oxygen storage via rare earth oxides. 

We have explored rare earth oxide-modified amorphous silica-aluminas as "permanent" intermediate strength acids used as supports for bifunctional catalysts. The addition of well dispersed weakly basic rare earth oxides "titrates" the stronger acid sites of amorphous silica-alumina and lowers the acid strength to the level shown by halided aluminas. Physical and chemical probes, as well as model olefin and paraffin isomerization reactions show that acid strength can be adjusted close to that of chlorided and fluorided aluminas. Metal activity is inhibited relative to halided alumina catalysts, which limits the direct metal-catalyzed dehydrocyclization reactions during paraffin reforming but does not interfere with hydroisomerization reactions. 

In both cases, we observe an amorphous pattern no crystallites of rare earth oxide appear even at 25% wt. loading. This indicates that oxide particles remain less than 30A in diameter. The surface area, pore volume and pore size distribution of the starting Si-Al support also change on impregnation. Table 1 lists the values for yttria-modified samples of... 

Fig. 5. Equimolar Rare Earth Oxide Concentration Display Similar Acid Strengths...

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