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Carbon glycerol

H. Chen, A. S. Ko wall, S. Majumdar, K. K. Sirkar, Selective CO2 separation from CO2-N2 mixtures by immobilised carbonate-glycerol membranes, Ind. Eng. Chem. Res. 38 (1999) 3489-3498. [Pg.355]

NO, NO2, and 0 were monitored continuously with a Monitor Labs dual channel chemiluminescence NO analyzer and an AID portable ozone analyzer. SO2 was determined with the carbonate-glycerol impregnated filter technique. HNO was determined by the denuder difference method (J[2). HCl was determined with the Na2C0o impregnated filter technique (j[3). The oxalic acid impregnated filter method (j[4) was used to determine NH. Total particulate was collected on 1-ym pore size Ghia Tefweb filters. Aqueous extracts of the filters were analyzed to determine particulate NO, S0 J, Cl , NHjJ, Ca, Mg", Na , and K" " concentrations. [Pg.94]

TGs are composed of a 3 carbon glycerol to which 3 fatty acids are esterified, and the glycerol carbons are stereo-specifically numbered as snl, sn2, and sn3 (Iimis 2011). The mammary gland actively uptakes FAs from plasma for the de novo synthesis of TGs (Neville and Picciano 1997), where, there is a preferential acylation of fatty acids to specific positions in TGs, making it seem as there is a biological purpose for investing in the enzymes needed to achieve the nonrandom positioning of TG fatty acids (Innis 2011). [Pg.146]

The majority of practical micellar systems of Tionnal micelles use water as tire main solvent. Reverse micelles use water immiscible organic solvents, altlrough tire cores of reverse micelles are usually hydrated and may contain considerable quantities of water. Polar solvents such as glycerol, etlrylene glycol, fonnamide and hydrazine are now being used instead of water to support regular micelles [10]. Critical fluids such as critical carbon dioxide are... [Pg.2575]

Required Glycerol, 70 ml. oxalic acid, 40 g. lead carbonate. [Pg.113]

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 ... [Pg.444]

Esters of glycerol called glycerol tnesters tnacylglycerols or triglycerides are abundant natural products The most important group of glycerol tnesters includes those m which each acyl group is unbranched and has 14 or more carbon atoms... [Pg.846]

Esters can participate m hydrogen bonds with substances that contain hydroxyl groups (water alcohols carboxylic acids) This confers some measure of water solubil ity on low molecular weight esters methyl acetate for example dissolves m water to the extent of 33 g/100 mL Water solubility decreases as the carbon content of the ester increases Fats and oils the glycerol esters of long chain carboxylic acids are practically insoluble m water... [Pg.846]

Acetyl coenzyme A is the biosynthetic precursor to the fatty acids, which most often occur naturally as esters Fats and oils are glycerol esters of long chain carboxylic acids Typically these chains are unbranched and contain even numbers of carbon atoms... [Pg.1101]

Fats and oils (Section 26 2) Tnesters of glycerol Fats are solids at room temperature oils are liquids Fatty acid (Section 26 2) Carboxylic acids obtained by hydro lysis of fats and oils Fatty acids typically have unbranched chains and contain an even number of carbon atoms in the range of 12-20 carbons They may include one or more double bonds... [Pg.1283]

Chlorine Ammonia, acetylene, alcohols, alkanes, benzene, butadiene, carbon disulflde, dibutyl phthalate, ethers, fluorine, glycerol, hydrocarbons, hydrogen, sodium carbide, flnely divided metals, metal acetylides and carbides, nitrogen compounds, nonmetals, nonmetal hydrides, phosphorus compounds, polychlorobi-phenyl, silicones, steel, sulfldes, synthetic rubber, turpentine... [Pg.1207]

Hypochlorites, salts of Urea, amines, anthracene, carbon, carbon tetrachloride, ethanol, glycerol, mercaptans, organic sulfides, sulfur, thiols... [Pg.1209]

Sodium peroxide Glacial acetic acid, acetic anhydride, aniline, benzene, benzaldehyde, carbon di-sulflde, diethyl ether, ethanol or methanol, ethylene glycol, ethyl acetate, furfural, glycerol, metals, methyl acetate, organic matter... [Pg.1212]

The alcoholysis reaction may be carried out either batchwise or continuously by treating the triglyceride with an excess of methanol for 30—60 min in a well-agitated reactor. The reactants are then allowed to settle and the glycerol [56-81-5] is recovered in methanol solution in the lower layer. The sodium methoxide and excess methanol are removed from the methyl ester, which then maybe fed directiy to the hydrogenolysis process. Alternatively, the ester may be distilled to remove unreacted material and other impurities, or fractionated into different cuts. Practionation of either the methyl ester or of the product following hydrogenolysis provides alcohols that have narrow carbon-chain distributions. [Pg.446]

Fatty acids derived from animal and vegetable sources generally contain an even number of carbon atoms siace they are biochemically derived by condensation of two carbon units through acetyl or malonyl coenzyme A. However, odd-numbered and branched fatty acid chains are observed ia small concentrations ia natural triglycerides, particularly mminant animal fats through propionyl and methylmalonyl coenzyme respectively. The glycerol backbone is derived by biospeciftc reduction of dihydroxyacetone. [Pg.122]


See other pages where Carbon glycerol is mentioned: [Pg.171]    [Pg.349]    [Pg.118]    [Pg.42]    [Pg.42]    [Pg.1817]    [Pg.50]    [Pg.617]    [Pg.349]    [Pg.350]    [Pg.125]    [Pg.140]    [Pg.471]    [Pg.524]    [Pg.38]    [Pg.39]    [Pg.30]    [Pg.62]    [Pg.171]    [Pg.349]    [Pg.118]    [Pg.42]    [Pg.42]    [Pg.1817]    [Pg.50]    [Pg.617]    [Pg.349]    [Pg.350]    [Pg.125]    [Pg.140]    [Pg.471]    [Pg.524]    [Pg.38]    [Pg.39]    [Pg.30]    [Pg.62]    [Pg.18]    [Pg.510]    [Pg.113]    [Pg.446]    [Pg.459]    [Pg.830]    [Pg.992]    [Pg.252]    [Pg.1072]    [Pg.1072]    [Pg.1008]    [Pg.447]    [Pg.12]    [Pg.117]    [Pg.132]    [Pg.134]    [Pg.382]    [Pg.21]   
See also in sourсe #XX -- [ Pg.195 ]




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Biomass glycerol carbonate synthesis

Glycerol as a carbon source

Glycerol as carbon source

Glycerol carbon dioxide

Glycerol carbonate

Glycerol carbonate

Glycerol carbonate butyrate

Glycerol carbonate propionate

Glycerol carbonate synthesis

Reaction of Carbon Dioxide or Urea with Glycerol

Synthesis of Glycerol Carbonate

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