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Water and aqueous solutions

Film coefficients for turbulent flow that exist on the outside or shell side of the conventional baffled shell and tube exchanger are correlated for hydrocarbons, organic compounds, water, aqueous solutions, and gases by... [Pg.101]

Membrane polymeric materials for separation applications are made of polyamide, polypropylene, polyvinylidene fluoride, polysulfone, polyethersulfone, cellulose acetate, cellulose diacetate, polystyrene resins cross-linked with divinylbenzene, and others (see Section 2.9) [59-61], The use of polyamide membrane filters is suggested for particle-removing filtration of water, aqueous solutions and solvents, as well as for the sterile filtration of liquids. The polysulfone and polyethersulfone membranes are widely applied in the biotechnological and pharmaceutical industries for the purification of enzymes and peptides. Cellulose acetate membrane filters are hydrophilic, and consequently, are suitable as a filtering membrane for aqueous and alcoholic media. [Pg.73]

The nonpolar nature of EPDM/PP TEOs make them highly resistant to water, aqueous solutions, and other polar fluids such as alcohols and glycols, but they swell excessively with toss of properties when exposed to halocarbons and hydrocarbons such as oils and fuels. Blends with NBR and PVC are more resistant to aggressive fluids with the exception of the halocarbons. [Pg.519]

Water, aqueous solutions and many other strongly hydrophilic substances can be solubilized within the micellar core [19,20], Water solubilization involves hydration of the surfactant headgroup accompanied by an increase in the head-group area, a micellar swelling, a marked increase in the surfactant aggregation number, and, at constant surfactant concentration, a decrease in the number density of reversed micelles [21], A representation of a spherical reverse micelle entrapping a polar solubilizate in the core is shown in Fig. 3. [Pg.4]

This article is based on the second and third of four lectures that I presented at the International Summer School of Biophysics. The first lecture, entitled Recent developments in the theory of water, aqueous solutions and protein hydration, has already been summarized in several review articles (Scheraga, 1979 Paterson et al., 1981 Nemethy et al., 1981), and the fourth lecture, entitled Enzyme - substrate interactions, has likewise been summarized in two recent reviews (Pincus and Scheraga, 1981 ... [Pg.45]

Fig. 11.37 Free energy profile for the nucleophilic attack of water on CO2 (a) in aqueous solution and (b) in the enzyme carbonic anhydrase. (Graphs redrawn from Aqvist J, M Fothergill and A Warshel 1993. Computer Simulai of the COj/HCOf Interconversion Step in Human Carbonic Anhydrase I. Journal of the American Chemical Society 115 631-635.)... Fig. 11.37 Free energy profile for the nucleophilic attack of water on CO2 (a) in aqueous solution and (b) in the enzyme carbonic anhydrase. (Graphs redrawn from Aqvist J, M Fothergill and A Warshel 1993. Computer Simulai of the COj/HCOf Interconversion Step in Human Carbonic Anhydrase I. Journal of the American Chemical Society 115 631-635.)...
Both chloramine-T and dichloramine-T have marked antiseptic properties, chloramine-T being most frequently used because of its solubility in water. Aqueous solutions of chloramine-T can be used either for external application, or for internal application to the mouth, throat, etc, as chloramine-T in moderate quantities is non-toxic its aqueous solution can also be effectively used when the skin has come in contact with many of the vesicant liquid poison-gases, as the latter are frequently organic sulphur or arsenic derivatives which combine with or are oxidised by chloramine-T and are thus rendered harmless. [Pg.253]

Sulphur. THE LASSAIGNE SODIUM TEST. The sodium fusion will have converted any sulphur present in the original compounds to sodium sulphide. Dissolve a few crystals of sodium nitroprusside, Na8[Fe(CN)5NO],zH20, in water, and add the solution to the third portion of the filtrate obtained from the sodium fusion. A brilliant purple coloration (resembling permanganate) indicates sulphur the coloration slowly fades on standing. Note, (i) Sodium nitroprusside is unstable in aqueous solution and therefore the solution should be freshly prepared on each occasion, (ii) This is a very delicate test for sulphides, and it is essential therefore that all apparatus, particularly test-tubes, should be quite clean. [Pg.325]

Both chloramine-T and dichloramine-T slowly liberate hypochlorous aeid in eontaet with water and are therefore employed as antiseptics the former is employed in the form of a dilute (e.g., 0-2 per eent.) aqueous solution, and the latter (which is insoluble in water) as a solution in an organic solvent, such as a chlorinated paraffin. [Pg.821]

To hydrolyse an ester of a phenol (e.g., phenyl acetate), proceed as above but cool the alkaline reaction mixture and treat it with carbon dioxide until saturated (sohd carbon dioxide may also be used). Whether a solid phenol separates or not, remove it by extraction with ether. Acidify the aqueous bicarbonate solution with dilute sulphuric acid and isolate the acid as detailed for the ester of an alcohol. An alternative method, which is not so time-consuming, may be employed. Cool the alkaline reaction mixture in ice water, and add dilute sulphuric acid with stirring until the solution is acidic to Congo red paper and the acid, if aromatic or otherwise insoluble in the medium, commences to separate as a faint but permanent precipitate. Now add 5 per cent, sodium carbonate solution with vigorous stirring until the solution is alkaline to litmus paper and the precipitate redissolves completely. Remove the phenol by extraction with ether. Acidify the residual aqueous solution and investigate the organic acid as above. [Pg.1064]

Perchlorates. Iron(II) perchlorate hexahydrate [13922-23-8], Fe(C10 2 6H20, is prepared by dissolving iron in cold, dilute perchloric acid or by dissolving FeS in perchloric acid. It crystallizes in hygroscopic, light green hexagonal prisms which are stable in dry air and extremely soluble (0.978 g/mL H2O at 0°C) in water and alcohol. It is susceptible to air oxidation in aqueous solution and decomposes above 100°C. Yellow iron(III) perchlorate... [Pg.437]

Amino-2-hydroxybenZOiC acid. This derivative (18) more commonly known as 4-aminosa1icy1ic acid, forms white crystals from ethanol, melts with effervescence and darkens on exposure to light and air. A reddish-brown crystalline powder is obtained on recrystallization from ethanol —diethyl ether. The compound is soluble ia dilute solutioas of nitric acid and sodium hydroxide, ethanol, and acetone slightly soluble in water and diethyl ether and virtually insoluble in benzene, chloroform or carbon tetrachloride. It is unstable in aqueous solution and decarboxylates to form 3-amiaophenol. Because of the instabihty of the free acid, it is usually prepared as the hydrochloride salt, mp 224 °C (dec), dissociation constant p 3.25. [Pg.315]

The amino group is readily dia2oti2ed in aqueous solution, and this reaction forms a basis for the assay of sulfas. Aldehydes also react to form anils, and the yellow product formed with 4-(dimethylamino)hen2a1dehyde can be used for detection in thiu-layer and paper chromatography. Chromatographic retention values have been deterrnined in a number of thiu layer systems, and have been used as an expression of the lipophilic character of sulfonamides (23). These values have corresponded well with Hansch lipophilic parameters determined in an isobutyl alcohol—water system. [Pg.466]

The mixture of diastereomers has been separated into its two principal components by Izatt, Haymore, Bradshaw and Christensen who had previously identified the two principal diastereomers as the cis-syn-cis and cis-anti-cis isomers. Their previous separation technique involved a protracted chromatography on alumina but the new method relied upon the difference in water solubility between the lead perchlorate and hydroniur perchlorate complexes. The lead perchlorate complex is essentially insoluble in aqueous solution and precipitates from it. Using this method, one may obtain 39% of the high-melting polymorph (mp 83—84°) and 44% of the low-melting compound (mp 62—63°). Note that the former also exists in a second crystalline form, mp 69—70°. [Pg.24]

The interactions between water and aqueous solutions and another phase have been modeled in various ways. The most simple models consist of an aqueous system in contact with a hard or soft wall described by... [Pg.353]


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