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Glycerol using

Table 3. Selective oxidation of glycerol using l%Au/C catalyst prepared via sol immobilisation. Table 3. Selective oxidation of glycerol using l%Au/C catalyst prepared via sol immobilisation.
In a number of experiments, the glycerol used contained an appreciable amount of water. Under these conditions, the yield of product is much lower. Dynamite glycerol containing less than half a per cent of water is best employed U. S. P. glycerol contains 5 per cent of water and usually gives lower yields. [Pg.42]

Glycerol, used for the production of alkyds, is produced by the catalytic hydroxylation or the hypochlorination of allyl alcohol. Allyl alcohol is produced by the reduction of acrolein, which is in turn obtained by the oxidation of propylene. [Pg.533]

Table 8.3 Production of dihydrogen from glycerol using strain K4 under anaerobic conditions". Table 8.3 Production of dihydrogen from glycerol using strain K4 under anaerobic conditions".
In the final reaction stage, epichlorohydrin is hydrolyzed to glycerol using a sodium hydroxide or sodium carbonate base ... [Pg.139]

A 100.0 g sample of glycerol is put into the calorimeter calibrated in Problem 6, and its temperature is observed to be 20.5°C. Then 45.7 g of iron at 165.0°C are added to the glycerol, giving a resultant temperature of 37.4°C. Calculate the specific heat of the glycerol. (Use the approximate specific heat of iron.)... [Pg.223]

Table 7.3 Carboxylation of glycerol using di (n-butyl)tindimethoxide as catalyst."... Table 7.3 Carboxylation of glycerol using di (n-butyl)tindimethoxide as catalyst."...
Sulfonic acids and sulfonate salts contain the -S03H and -SO) groups, respectively, attached to a hydrocarbon moiety. The structural formulas of benzene sulfonic acids and of sodium 1 -(p-sulfophenyl)decane, a biodegradable detergent surfactant, are shown in Figure 1.19. The common sulfonic acids are water-soluble strong acids that lose virtually all ionizable H+ in aqueous solution. They are used commercially to hydrolyze fat and oil esters to produce fatty acids and glycerol used in chemical synthesis. [Pg.52]

Palkovits R, Nieddu I, Kruithof CA, Klein-Gebbink RJM, Weckhuysen BM (2008) Palladium-based telomerization of 1,3-butadiene with glycerol using methoxy-functionalized triphenylphosphine ligands. Chem Eur J 14 8995-9005... [Pg.96]

The loss in weight is dependent upon the quality of the arsenic oxide and glycerol used. If these are dry, the weight loss should be as indicated. The lower figure is equivalent to 1 mole of water for each mole of glycerol. [Pg.51]


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