Magnesium oxide formation

Formation of a gelatinous precipitate that is difficult to filter can be avoided by addition of magnesium oxide to the acid solution. In order to increase particle size it is often necessary to keep the solution hot for several hours however, this problem is avoided by heating an intimate mixture of ammonium bifluoride with magnesium carbonate to 150—400°C (11). Particles of Mgp2 similar in size to those of the magnesium carbonate are obtained. 

For binder preparation, dilute hydrochloric or acetic acids are preferred, because these faciUtate formation of stable silanol condensation products. When more complete condensation or gelation is preferred, a wider range of catalysts, including moderately basic ones, is employed. These materials, which are often called hardeners or accelerators, include aqueous ammonia, ammonium carbonate, triethanolamine, calcium hydroxide, magnesium oxide, dicyclohexylamine, alcohoHc ammonium acetate, and tributyltin oxide (11,12). 

Ethjl Silicate-Bonded Investments. These investments are mixtures of powder and Uquid. The powder consists of refractory particles of sUica glass, crystobahte, and other metal oxides plus magnesium oxide. The Uquid is a hydrated sUica, tetrasUicic acid [10193-36-9] Si [OH], that is suppUed in a stabUized form it can be developed by mixing ethyl sUicate [78-10 ] denatured ethyl alcohol [64-17-5] and hydrochloric acid [7647-01 -OJ. The binding of the powder is accompUshed by the formation of a sUica gel according to the reaction ... 

The high heat resistance produced by adding phenolic resins to solvent-borne CR adhesives is due to the formation of the infusible resinate, which reduces the thermoplasticity of the adhesive and provides good bond strength up to 80°C (Table 11). The resinate also increases the adhesive bond strength development by accelerating solvent release. 4 phr of magnesium oxide for 40 phr of phenolic resin are sufficient to produce a room temperature reaction. A small amount of water (1-2 phr) is necessary as a catalyst for the reaction. Furthermore, the solvent... 

For all three halates (in the absence of disproportionation) the preferred mode of decomposition depends, again, on both thermodynamic and kinetic considerations. Oxide formation tends to be favoured by the presence of a strongly polarizing cation (e.g. magnesium, transition-metal and lanthanide halates), whereas halide formation is observed for alkali-metal, alkaline- earth and silver halates. 

A detailed study of the dehydrogenation of 10.1 l-dihydro-5//-benz[6,/]azcpinc (47) over metal oxides at 550 C revealed that cobalt(II) oxide, iron(III) oxide and manganese(III) oxide are effective catalysts (yields 30-40%), but formation of 5//-dibenz[7),/]azepinc (48) is accompanied by ring contraction of the dihydro compound to 9-methylacridine and acridine in 3-20 % yield.111 In contrast, tin(IV) oxide, zinc(II) oxide. chromium(III) oxide, cerium(IV) oxide and magnesium oxide arc less-effective catalysts (7-14% yield) but provide pure 5H-dibenz[b,/]azepine. On the basis of these results, optimum conditions (83 88% selectivity 94-98 % yield) for the formation of the dibenzazepine are proposed which employ a K2CO,/ Mn203/Sn02/Mg0 catalyst (1 7 3 10) at 550 C. 

As we have already shown, the presence of cations in orthophosphoric acid solution can have a decisive effect on cement formation. As noted above, Kingery (1950b) found it necessary to modify orthophosphoric add, by the addition of calcium, to obtain cement formation with calcium oxide. Also, Finch and Sharp (1989) had to modify orthophosphoric add, with either ammonium or aluminium, to achieve cement formation with magnesium oxide. 

Figure 5.5.1 Formation of a white magnesium oxide coating as magnesium ribbon reacts with oxygen. From Masterton and Hurley, Chemistry Principles and Reactions, 4th edition. Orlando Harcourt, 2001. Photo courtesy of Charles D. Winters. 

In this paper we will focus on two materials magnesium oxide and molybdenum highly dispersed on silica. The formation of oxygen anions requires electrons at a high potential. On magnesium oxide these electrons are present as Fs centers, which are formed by irradiation ( X = 254 nm) of a degassed sample in the presence of H2 (5). On Mo/Si02 the electrons are derived by the oxidation of Mo(V) to Mo(VI) (6,7). 

Garrone, E. Zecchina, A. Stone, F.S. Anionic intermediates in surface processing leading to ()2 formation on magnesium oxide. J. Catal. 1980, 62, 396 100. 

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