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Inorganic salts solubility

The cobalt catalyst can be introduced into the reactor in any convenient form, such as the hydrocarbon-soluble cobalt naphthenate [61789-51 -3] as it is converted in the reaction to dicobalt octacarbonyl [15226-74-17, Co2(CO)g, the precursor to cobalt hydrocarbonyl [16842-03-8] HCo(CO)4, the active catalyst species. Some of the methods used to recover cobalt values for reuse are (11) conversion to an inorganic salt soluble ia water conversion to an organic salt soluble ia water or an organic solvent treatment with aqueous acid or alkah to recover part or all of the HCo(CO)4 ia the aqueous phase and conversion to metallic cobalt by thermal or chemical means. [Pg.458]

Solubility of low molecular weight gas goes down with temperature, but inorganic salt solubility goes up with temperature ... [Pg.208]

Note Colorless, odorless (when pure), hygroscopic liquid, powerful aprotic solvent dissolves many inorganic salts, soluble in water combustible readily penetrates the skin incompatible with strong oxidizers and many halogenated compounds (e.g., alkyl halides, aryl halides), oxygen, peroxides, diborane, perchlorates. Synonyms DMSO, methyl sulfoxide, sulfinylbismethane. [Pg.343]

In certain compounds, especially inorganic salts, solubility may not be affected or may actually decrease at higher temperatures. A good example is calcium carbonate water (hardwater), which has lower solubility at higher temperatures. This reverse solubihty behavior causes troublesome scale deposits issue in hot water boilers because water is maintained at a higher temperature in the water boiler. Therefore, calcium carbonate becomes supersaturated and precipitates in the boiler. In the authors experience, however, reverse solubihty is very rare in fine organics or pharmaceuticals. [Pg.16]

Substances are generally soluble in like solvents. Organic molecules in molecular solvents such as CCI4, C2H5OH, ether, propanone. Inorganic salts are often soluble in water and less soluble in organic solvents. [Pg.366]

In the isolation of organic compounds from aqueous solutions, use is frequently made of the fact that the solubility of many organic substances in water is considerably decreased by the presence of dissolved inorganic salts (sodium chloride, calcium chloride, ammonium sulphate, etc.). This is the so-called salting-out effect. A further advantage is that the solubility of partially miscible organic solvents, such as ether, is considerably less in the salt solution, thus reducing the loss of solvent in extractions. [Pg.151]

The high sodium ion concentration results in facile crystallisation of the sodium salt. This process of salting out with common salt may be used for recrystallisation, but sodium benzenesulphonate (and salts of other acids of comparable molecular weight) is so very soluble in water that the solution must be almost saturated with sodium chloride and consequently the product is likely to be contaminated with it. In such a case a pure product may be obtained by crystallisation from, or Soxhlet extraction with, absolute alcohol the sul-phonate is slightly soluble but the inorganic salts are almost insoluble. Very small amounts of sulphones are formed as by-products, but since these are insoluble in water, they separate when the reaction mixture is poured into water ... [Pg.548]

The essential basis of the scheme for the separation of water-soluble compounds is, therefore, distillation of (a) an aqueous solution of the mixture, (b) an alkaline (with sodium hydroxide) solution of the mixture, and (c) an acidic (with sulphuric oj phosphoric acid) solution of the mixture. The residue will contain the non-volatile components, which must be separated from inorganic salts and from each other by any suitable process. [Pg.1092]

To ensure that reaction occurs m homogeneous solution solvents are chosen that dis solve both the alkyl halide and the ionic salt The alkyl halide substrates are soluble m organic solvents but the salts often are not Inorganic salts are soluble m water but alkyl... [Pg.327]

Two inorganic water-soluble polymers, both polyelectrolytes in their sodium salt forms, have been known for some time poly(phosphoric acid) (12) and poly(siHcic acid) (13). A more exciting inorganic water-soluble polymer with nonionic... [Pg.318]

Hitec Heat-Transfer Salt. Hitec heat-transfer salt, manufactured by Coastal Chemical Co., is an eutectic mixture of water-soluble inorganic salts potassium nitrate (53%), sodium nitrite (40%), and sodium nitrate (7%). It is suitable for Hquid-phase heat transfer at temperatures of 150—540°C. [Pg.504]

Physical and ionic adsorption may be either monolayer or multilayer (12). Capillary stmctures in which the diameters of the capillaries are small, ie, one to two molecular diameters, exhibit a marked hysteresis effect on desorption. Sorbed surfactant solutes do not necessarily cover ah. of a sohd iaterface and their presence does not preclude adsorption of solvent molecules. The strength of surfactant sorption generally foUows the order cationic > anionic > nonionic. Surfaces to which this rule apphes include metals, glass, plastics, textiles (13), paper, and many minerals. The pH is an important modifying factor in the adsorption of all ionic surfactants but especially for amphoteric surfactants which are least soluble at their isoelectric point. The speed and degree of adsorption are increased by the presence of dissolved inorganic salts in surfactant solutions (14). [Pg.236]

As may be expected of an amorphous polymer in the middle range of the solubility parameter table, poly(methyl methacrylate) is soluble in a number of solvents with similar solubility parameters. Some examples were given in the previous section. The polymer is attacked by mineral acids but is resistant to alkalis, water and most aqueous inorganic salt solutions. A number of organic materials although not solvents may cause crazing and cracking, e.g. aliphatic alcohols. [Pg.409]

The alcoholic ethereal filtrate is then dried over calcined potassium carbonate and the solution evaporated, whereby 0.9 to 1 part of a mixture of d-lysergic acid-d-l-hydroxybutyl-amide-2 and of d-isolysergic acid-d-l-hvdroxvbutylamide-2 is obtained. In order to separate the isomers, the residue is dissolved in 15 parts of hot chloroform and filtered from the small quantity of inorganic salt, whereby on cooling down, the difficultly soluble chloroform compound of d-lysergic acid-d-l hvdroxvbutylamide-2 crystallizes out. Yield 0.4 part. This compound can be recrystallized from hot benzene, whereby crystals melting... [Pg.994]

In most cases diazonium salts are not isolated, but are converted into products by reactions that can be carried out in situ. Moreover, it is actually recommended not to isolate these salts, not even for purification purposes, as many of them have a tendency to explode. In addition, the high solubility of most diazonium salts in water makes precipitation from this medium difficult. Therefore, to obtain solid diazonium salts the recommended method for many decades was to carry out diazotizations in ethanol followed by precipitation with ether. As inorganic salts of nitrous acid are scarely soluble in ethanol, Knoevenagel recommended alkyl nitrites (ethyl or isopentyl nitrite) as diazotization reagents as long ago as 1890. Various other solvents have subsequently been used for diazotizations with alkyl nitrites (see Saunders and Allen, 1985, p. 23 ff.), but as a method for obtaining solid diazonium salts this has been superseded by the isolation of diazonium tetrafluoroborates and, to a lesser degree, of hexafluorophosphates. [Pg.25]

The facile solubility of inorganic salts in DMSO is considered to be due to the strong solvation of the cations resulting in the formation of naked anions . [Pg.545]

This chapter describes several Important applications of aqueous equilibria. We begin with a discussion of buffer chemistry, followed by a description of acid and base titration reactions. Then we change our focus to examine the solubility equilibria of inorganic salts. The chapter concludes with a discussion of the equilibria of complex Ions. [Pg.1273]

Transfer of the hydride from the Cu to the electrophilic carbon and cleavage of the copper alkoxide by the silane regenerates 69. Recent reports point to the influence of the type of the counter ion X" of the homoleptic 66-67 on the activity, the BF being superior to the PF analogue this effect has been attributed to differences in the rate of active catalyst generation from the homoleptic [Cu(NHC)2] X and NaO Bu due to solubility differences of the inorganic salts formed during the displacement of the NHC by BuO" [54] (Scheme 2.10). [Pg.37]

The concentration of a compound in water is controlled by its equilibrium solubility or solubility constant (the maximum amount of a compound that will dissolve in a solution at a specified temperature and pressure). Equilibrium solubility will change with environmental parameters such as temperature, pressure, and pH for example, the solubility of most organic compounds triples when temperature rises from 0°C to 30°C. Each type of waste has a specific equilibrium solubility at a given temperature and pressure. The solubility of toxic organic compounds is generally much lower than that of inorganic salts. This characteristic is particularly true of nonpolar compounds because of their hydrophobic character. [Pg.796]

Chemicals of various types are used in every stage of drilling, completing, and producing oil and gas wells. This review describes these chemicals, why they are used, and recent developments. These chemicals include common inorganic salts, transition metal compounds, common organic chemicals and solvents, water-soluble and oil-soluble polymers, and surfactants. As existing fields become depleted, use of chemistry to maintain production via well stimulation, more efficient secondary recovery operations, and enhanced oil recovery become ever more important. [Pg.9]

Chitosan features far more than chitin in research into applications. This is largely due to their difference in solubility characteristics, chitosan being more amenable to practical manipulation. Chitin is in fact rather more intractable than cellulose, since it is insoluble in those solvents, such as cuprammonium hydroxide, that are commonly used to dissolve cellulose. Chitin is soluble in hot concentrated solutions of certain inorganic salts capable of... [Pg.73]


See other pages where Inorganic salts solubility is mentioned: [Pg.43]    [Pg.37]    [Pg.43]    [Pg.37]    [Pg.164]    [Pg.435]    [Pg.224]    [Pg.167]    [Pg.74]    [Pg.166]    [Pg.386]    [Pg.386]    [Pg.466]    [Pg.292]    [Pg.1655]    [Pg.154]    [Pg.5]    [Pg.93]    [Pg.227]    [Pg.163]    [Pg.435]    [Pg.565]    [Pg.625]    [Pg.467]   
See also in sourсe #XX -- [ Pg.25 ]




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