Glycerol aqueous

Experimental determination of velocity profiles in films flowing on vertical tube by stereoscopic chronophoto-graphic method. Films included glycerol, aqueous glycerol solutions, liquid paraffin, glycerol + surfactant. In smooth flow, profiles agreed with theoretical semi-... 

Fig.6 Changes in concentration of thermolysin during crystallization carried out in 20 w% glycerol aqueous solution. Crystallization conditions 15 mg/mL thermolysin, pH 7.0 and 5 C. ( ) filtrate A, (O) filtrate B.

Fig.9 DSC curves for suspensions of thermolysin crystal. Initial concentration of thermolysin 7 (above) and 12 m mL (below). Solvent 20 w% glycerol aqueous solution (pH 7.0, 5 °C). Crystallization time 0.5 h. Temperature scanning rate 10°C/h.

Ruiz, C.C., L. Diaz-Lopez, and J. Aguiar. 2008. Micellization of sodium dodecyl sulfate in glycerol aqueous mixtures. Journal of Dispersion Science and Technology 29(2) 266-273. Santos, A., J.A. Toledo-Femandez, R. Mendoza-Sema, L. Gago-Duport, N. de la Rosa-Fox, M. Pinero, and L. Esquivias. 2006. Chemically active silica aerogel— wollastonite composites for CO2 fixation by carbonation reactions. Industrial and Engineering Chemistry Research 46(1) 103-107. 

Dissolve 0 5 ml. of glycerol in 20 ml. of w ater, and add 20 ml. of the above 5% aqueous sodium periodate solution. After 15-20 minutes add 12 ml. of the above 10% ethanolic dimedone solution, and stir well at intervals for another 15 minutes. The addition of the dimedone solution may cause a rapid precipitation of some of the dimedone itself, which is only slightly soluble in water, whereas the formaldehyde-dimedone compound separates more slowly from the solution. 

Polyhydric alcohols are compounds containing two or more hydroxyl groups in the molecule. The two most important are ethylene glycol HOCHjCHjOH (a dihydric alcohol) and glycerol HOCHjCH(OH)CH. OH (a trihydric alcohol). Ethylene glycol may be obtained by the hydrolysis of ethylene dibromide or ethylene dichloride with dilute aqueous sodium hydroxide or sodium carbonate solution ... 

Pyrolysis of the methylamine salt (produced by neutralising mucic acid with aqueous methylamlne) in the presence of glycerol yields JV-methylpyrrole ... 

Tnmynstm is obtained from coconut oil and has the molecular formula C45H86O6 On being heated with aqueous sodium hydroxide followed by acidification trimyristin was converted to glycerol and tetradecanoic acid as the only products What is the structure of trimyristin ... 

Animal fats and vegetable oils are triacylglycerols, or triesters, formed from the reaction of glycerol (1,2, 3-propanetriol) with three long-chain fatty acids. One of the methods used to characterize a fat or an oil is a determination of its saponification number. When treated with boiling aqueous KOH, an ester is saponified into the parent alcohol and fatty acids (as carboxylate ions). The saponification number is the number of milligrams of KOH required to saponify 1.000 g of the fat or oil. In a typical analysis, a 2.085-g sample of butter is added to 25.00 ml of 0.5131 M KOH. After saponification is complete, the excess KOH is back titrated with 10.26 ml of0.5000 M HCl. What is the saponification number for this sample of butter ... 

MetaUic ions are precipitated as their hydroxides from aqueous caustic solutions. The reactions of importance in chlor—alkali operations are removal of magnesium as Mg(OH)2 during primary purification and of other impurities for pollution control. Organic acids react with NaOH to form soluble salts. Saponification of esters to form the organic acid salt and an alcohol and internal coupling reactions involve NaOH, as exemplified by reaction with triglycerides to form soap and glycerol,... 

Water-Based Writing Inks. These consist of very fine pigment dispersions in aqueous media containing small amounts of glycol or glycerol and a dispersing aid. They dry mainly by evaporation and quick wetting of ceUulosic fibers in paper substrates. 

In the reaction of aEyl alcohol with an aqueous chlorine solution, addition of hypochlorous acid to the double bond of aEyl alcohol yields glycerol monochlorohydrin and as a by-product, glycerol dichlorohydrin. Thus, a poor yield of glycerol monochlorohydrin is obtained (8). To improve the yield of glycerol monochlorohydrin, addition of sodium carbonate in an amount equivalent to that of the hydrogen chloride in the aqueous chlorine solution, has been proposed (9). 

Methyl formate and propylene oxide have close boiling poiats, making separation by distillation difficult. Methyl formate is removed from propylene oxide by hydrolysis with an aqueous base and glycerol, followed by phase separation and distillation (152,153). Methyl formate may be hydrolyzed to methanol and formic acid by contacting the propylene oxide stream with a basic ion-exchange resia. Methanol and formic acid are removed by extractive distillation (154). 

Rosin ester resins are used extensively in pressure-sensitive adhesives as tackifiers. The adhesive is formulated by blending the resin with a polymer in solution or as aqueous emulsions. Typical compositions may contain about 50% resin. The glycerol or pentaerythritol esters of stabilized rosins are often used because they are stable on aging. 

Carboxylate soaps are most commonly formed through either direct or indirect reaction of aqueous caustic soda, ie, alkaH earth metal hydroxides such as NaOH, with fats and oils from natural sources, ie, triglycerides. Fats and oils are typically composed of both saturated and unsaturated fatty acid molecules containing between 8 and 20 carbons randomly linked through ester bonds to a glycerol [56-81-5] backbone. Overall, the reaction of caustic with triglyceride yields glycerol (qv) and soap in a reaction known as saponification. The reaction is shown in equation 1. 

The acid occurs both as colorless triclinic prisms (a-form) and as monoclinic prisms ( 3-form) (8). The P-form is triboluminescent and is stable up to 137°C the a-form is stable above this temperature. Both forms dissolve in water, alcohol, diethyl ether, glacial acetic acid, anhydrous glycerol, acetone, and various aqueous mixtures of the last two solvents. Succinic acid sublimes with partial dehydration to the anhydride when heated near its melting point. 

The structure of these products is uncertain and probably depends on pH and concentrations in solution. The hydroxyl or carboxyl or both are bonded to the titanium. It is likely that most, if not all, of these products are oligomeric in nature, containing Ti—O—Ti titanoxane bonds (81). Thek aqueous solutions are stable at acidic or neutral pH. However, at pH ranges above 9.0, the solutions readily hydroly2e to form insoluble hydrated oxides of titanium. The alkaline stabiUty of these complexes can be improved by the addition of a polyol such as glycerol or sorbitol (83). These solutions are useful in the textile, leather (qv), and cosmetics (qv) industries (see Textiles). 

Sodium hen ate [532-32-1], C H COONa, is highly soluble in water (61.2 g dissolve in 100 g of water at 25°C) and somewhat soluble in ethyl alcohol, glycerol, and methanol. A 25% aqueous solution of sodium benzoate exhibits a pH of 7.5—8. 

---