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Distillation of water

Bromohydrins can be prepared direcdy from polyhydric alcohols using hydrobromic acid and acetic acid catalyst, followed by distillation of water and acetic acid (21). Reaction conditions must be carehiUy controlled to avoid production of simple acetate esters (22). The raw product is usually a mixture of the mono-, di-and tribromohydrins. [Pg.464]

In nature, oxygen occurs in three stable isotopic species oxygen-16 [14797-70-7] O, 99.76% oxygen-17 [13968-48-4], 0.038% and oxygen-18 [14797-71-8], 0.20% (7). Commercial fractional distillation of water produces concentrations of as high as 99.98% concentrations up to 55% are also produced. The isotope has been used to trace mechanisms of organic reactions. [Pg.475]

British Columbia, and three at the U.S. Army Ordinance Works operated by the DuPont Company at Morgantown, West Virginia Cluldersburg, Alabama and Dana, Indiana. The plant at Trail used chemical exchange between hydrogen gas and steam for the initial isotope separation followed by electrolysis for final concentration. The three plants in the United States used vacuum distillation of water for the initial separation followed by electrolysis. Details of these plants and their operations may be found in the Hterature (10). [Pg.3]

In the heavy-water plants constmcted at Savannah River and at Dana, these considerations led to designs in which the relatively economical GS process was used to concentrate the deuterium content of natural water to about 15 mol %. Vacuum distillation of water was selected (because there is Httle likelihood of product loss) for the additional concentration of the GS product from 15 to 90% D2O, and an electrolytic process was used to produce the final reactor-grade concentrate of 99.75% D2O. [Pg.7]

To a 50-mL three-necked flask (Fig. 3.18b) equipped with a stirrer (comprised of a stainless steel shaft and paddle), a head for the distillation of water, and a nitrogen inlet is added 20 g of purified 11-aminoundecanoic acid. The flask is then purged with nitrogen for 5 min. The flask is warmed in a silicon oil bath to 220° C and maintained at this temperature for 10 h. After raising the stirrer from the molten mass, the reaction is cooled under nitrogen and the resultant polymer removed by breaking the glass. The Tm of the polymer is 185—190° C and the rjmh in m-cresol (0.5% at 35°C) is 0.6—0.7. [Pg.179]

Unfortunately, most of Kitaibel s work was never published, but his manuscripts preserved at the Hungarian National Museum in Budapest show that he was an ingenious designer of chemical apparatus, such as a salt-evaporating pan which utilized the heat of the fuel gas on the countercurrent principle a device for the saturation of mineral water with carbon dioxide apparatuses for vacuum filtration and for the distillation of water and an improved lime kiln and brick kiln (12). [Pg.335]

DOM is derived from autochthonous sources such as phytoplankton and photosynthetic bacteria (16) at Big Soda Lake near Fallon, Nevada. This lake is alkaline (pH 9.7) and chemically stratified. It contains DOC concentrations as high as 60 mg/L and dissolved salt concentrations as high as 88,000 mg/ L (17). The DOM in this lake is colorless. The fulvic acid fraction was isolated by adsorption chromatography (Amberlite XAD-8 resin) (18) and by zeo-trophic distillation of water from N,N-dimethylformamide (19). Average molecular model synthesis was achieved in a manner similar to that used for fulvic acid from the Suwannee River. The characterization data are presented in Table I and the structural model is presented in Structure 2. [Pg.201]

Subsequent researchers introduced substantial improvements on the Ueno and Okawara s protocol of selective oxidations via tin alkoxides and broadened considerably the scope of its application.223 24b,c Thus, it was established that good yields in the selective oxidation of diols—and even triols and tetrols can be achieved in two steps i) pre-formation of a tin alkoxide, by reaction with either (Bu3Sn)20 or Bu2SnO with elimination of water by molecular sieves or azeotropic distillation of water ii) treatment of the tin alkoxide with Br2 or NBS in the presence of a HBr quencher. [Pg.344]

When a solution is boiled, the water vapour escapes leaving behind the solid impurities. The vapour sent through a condenser is converted back to water. This process is called distillation of water. Distilled water has no odour, flavour or colour. [Pg.154]

Oxygen occurs in Nature in three isotopic species 160 (99.759%), nO (0.0374%), and 180 (0.2039%). The rare isotopes, particularly lsO, can be concentrated by fractional distillation of water, and concentrates containing up to 99 at. % lsO or up to 90 at. % nO as well as other labeled compounds are commercially available. Oxygen-18 has been widely used as a tracer in studying reaction mechanisms of oxygen compounds. Oxygen-17 has a nuclear spin 5/2, but because of the low abundance of this isotope and appreciable quadrupole moment, enriched materials and Fourier transform nmr techniques are required. [Pg.449]

The yields of desired products have been improved by the azeotropic distillation of water from the reaction mixture and the resultant H ion neutralization. [Pg.14]

The solution, on heating at 40 mm pressure, hydrolyses and a distillate of water and H2O2 is obtained ... [Pg.383]

Triethylenetetramine was purchased from Aldrich Chemical Company, Inc., as a hydrate. Anhydrous triethylenetetramine must be used in this procedure. The anhydrous tetraamine was obtained by azeotropic distillation of water (Dean-Stark trap, 3 days) from a solution of 125 g of the commercial hydrate in 150 mL of toluene. Analysis by 1H NMR verified the removal of water, and no further purification was necessary. [Pg.183]

Homopolymers of branching multifunctional monomers have also been reported. Aliphatic polyesters were prepared by condensing a polyhydroxy monocarboxylic acid of formula (HO)n-R-COOH, for example, 2,2-di(hydroxymethyl)propionic acid, in either DMF or xylene in the presence of an acid catalyst with azeotropic distillation of water. Since these polymers have a large number of functional groups, they are... [Pg.141]

Ballestra S.P.A., Italy has suggested that the process of making sodium toluene sulfonate can be improved by removing water formed from the sulfonation reactors by azeotropic distillation of water-toluene mixture along with excess of toluene required (necessary to form the proper mole ratio of water/toluene). Toluene along with water is condensed as an azeotrope from the distillation column and then recovered toluene is recycled back to the sulfonators. By using this process, less of toluene and H2SO4 will be required for the process of sulfonation. [Pg.27]

Pinacol (anhydrous) [76-09-5] M 118.1, m 41.1 , b 172. The hydrate is rendered anhydrous by azeotropic distillation of water with benzene. Recrystallise it from benzene or toluene/pet ether, absolute EtOH or dry diethyl ether. It recrystaUises from water to give the hexahydrate. [Beilstein 1IV 2575.]... [Pg.174]

Preparation of Oxygen — Breaking Glass Tubing — Catalytic Agents—Experiments with Oxygen—Production of Chlorine —Experiments with Chlorine—Neutralization—Distillation of Water — Practical Distillation — Thermit —A Small Electric... [Pg.2]

The apparatus necessary for the distillation of water is shown in Fig. 31. The condenser is a simple device, and is in need of very little description. It consists of a large glass tube with a rubber cork in each end. Two holes are in each of the rubber corks to permit... [Pg.22]


See other pages where Distillation of water is mentioned: [Pg.198]    [Pg.6]    [Pg.8]    [Pg.41]    [Pg.604]    [Pg.66]    [Pg.9]    [Pg.415]    [Pg.247]    [Pg.300]    [Pg.59]    [Pg.246]    [Pg.274]    [Pg.10]    [Pg.87]    [Pg.284]    [Pg.289]    [Pg.67]    [Pg.789]    [Pg.146]    [Pg.421]    [Pg.448]    [Pg.430]    [Pg.140]    [Pg.3]    [Pg.705]    [Pg.32]    [Pg.6]    [Pg.20]    [Pg.22]   
See also in sourсe #XX -- [ Pg.4 , Pg.114 , Pg.268 ]

See also in sourсe #XX -- [ Pg.4 , Pg.114 , Pg.268 ]




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