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Aqueous solutions of salts

A look at Table 3.1 shows that there are several types of salts. [Pg.108]

These are formed by the neutralisation of a strong acid with a strong base and are simply dealt with. The salt formed by the neutralisation of HCl(aq) with NaOH(aq) exists solely as the ions Na+(aq) and Cl (aq). Neither of these ions is involved in any acid/base behaviour with water since HCl(aq) and NaOH(aq) are a strong acid and strong base respectively, and are fully ionised in solution. The pH of the solution is governed by the self ionisation of water and, at 25°C, is equal to 7.00. [Pg.108]

In contrast, the salt formed by the neutralisation of methanoic acid, HCOOH(aq), with NaOH(aq) gives a basic solution with the pH dependent on the concentration of the salt. Sodium methanoate is the salt of a weak acid and strong base, and in the solid consists of Na and HCOO ions. When dissolved in water, Na (aq) ions show no acid/base behaviour with the water since NaOH(aq) is a strong base consisting of Na (aq) ions and OH (aq) ions only. However, HCOO (aq) is the conjugate base of the weak acid HCOOH(aq), and will thus accept a proton from the solvent water to form the undissociated acid HCOOH(aq) in the [Pg.108]

This is a basic solution since OH (aq) is formed, and this is why salts of a weak acid/strong base always have basic pH values. [Pg.109]

As mentioned in Section 3.10, pATb for the methanoate ion HCOO (aq) sometimes may not be tabulated, but instead may have to be worked out from the acid ionisation constant p Ta for the acid methanoic acid, HCOOH. [Pg.109]


Arrhenius, insofar as his profession could be defined at all, began as a physicist. He worked with a physics professor in Stockholm and presented a thesis on the electrical conductivities of aqueous solutions of salts. A recent biography (Crawford 1996) presents in detail the humiliating treatment of Arrhenius by his sceptical examiners in 1884, which nearly put an end to his scientific career he was not adjudged fit for a university career. He was not the last innovator to have trouble with examiners. Yet, a bare 19 years later, in 1903, he received the Nobel Prize for Chemistry. It shows the unusual attitude of this founder of physical chemistry that he was distinctly surprised not to receive the Physics Prize, because he thought of himself as a physicist. [Pg.26]

Aqueous solutions of salts with non-coordinating anions contain the pale-pink, [Mn(H20)6] +, ion which is one of a variety of high-spin octahedral complexes which have been... [Pg.1060]

In the crystallization of these hydrated salts from aqueous solutions it is essential that a low pH (high level of acidity) is maintained, otherwise hydrolysis occurs and yellow impurities contaminate the products. Similarly, if the salts are redissolved in water, the solutions turn yellow/brown. The hydrolytic processes are complicated, and, in the presence of anions with appreciable coordinating tendencies, are further confused by displacement of water from the coordination sphere of the iron. However, in aqueous solutions of salts such as the perchlorate the following equilibria are important ... [Pg.1089]

Obviously, water, aqueous solutions of salts, and mixtures of highly hydrophilic solvents have also been found to be solubilized in the micellar core [13,44]. The maximum amount of such solubilizates that can be dissolved in reversed micelles varies widely, strongly depending on the nature of the surfactant and the apolar solvent, on the concentrations of surfactant and of additives, and on temperature [24,45-47]. [Pg.478]

Other nylons, such as types 6 and 610, can behave differently, e.g. towards aqueous solutions of salts. [Pg.935]

Although the yields are lower, it is possible to use even aqueous solutions of salts of amino acids in the second step. The first step, however, must be carried out under anhydrous conditions. Usually the reaction is carried out as a one-pot procedure. [Pg.151]

Keeping in mind the above studies of multivalent cations (Fe, Cr and Mn) in aqueous medium, some experiments involving redox or complexometric reactions of these metal ions have been carried out, using ultrasound (20 kHz) and its effect on the precipitation, oxidation, reduction and decomposition of complex have been evaluated. An Ultrasonic Processor model P2 with a titanium tip of diameter 12 mm and 250 watts power was used. In the subsequent sections details of some of the interesting experiments, carried out in aqueous solutions of salts of Fe, Cr and Mn in their different oxidation states, have been discussed. [Pg.277]

Producing sweat is one of the body s natural ways of cooling itself, and it operates as follows. Sweat is an aqueous solution of salt and natural oils, and is secreted by glands just below the surface of the skin. The glands generate this mixture whenever the body feels too hot. Every time air moves over a sweaty limb, from a mechanical fan or natural breeze, the skin feels cooler following evaporation of water from the sweat. [Pg.81]

Temperature, pressure, and concentration can affect phase equilibria in a two-component or binary system, although the effect of pressure is usually negligible and data can be shown on a two-dimensional temperature-concentration plot. Three basic types of binary system — eutectics, solid solutions, and systems with compound formation—are considered and, although the terminology used is specific to melt systems, the types of behaviour described may also be exhibited by aqueous solutions of salts, since, as Mullin 3-1 points out, there is no fundamental difference in behaviour between a melt and a solution. [Pg.830]

The Arrhenius theory also has limitations for explaining certain reactions. For example, aqueous solutions of ammonia are basic. They react with acids in neutralization reactions, even though ammonia does not contain the hydroxide ion. Many aqueous solutions of salts with no hydroxide ions are basic, too. Some reactions take place without any liquid solvent. For example, ammonium chloride can be formed by the reaction between ammonia and hydrogen chloride, which are both gases ... [Pg.379]

For aqueous solutions of salts, lt, (P, 7) represents the chemical potential of pure ions. This chemical potential cannot be measnred experimentally. Instead of nsing this hypothetical standard state, the activity coefficients of ions often are normalized by introducing the asymmetrical activity coefficient, y,, defined as... [Pg.32]

Schultz IG, Shepard AO, Blackmon PD, Starkey HC (1971) Mixed layer kaoUnite-montmoriUon-ite from the Yucatan Peninsula, Mexico Clays Clay Miner 19 137-150 Shternina EB (1960) Solubility of gypsum in aqueous solutions of salts. Intern Geol Rev 1 pp 605-616... [Pg.375]

Elemental composition (for anhydrous NiCb) Ni 45.30%, Cl 54.70% Percent composition of NiCl2 6H20 Ni 24.69%, Cl 29.83%, H2O 45.48%. Nickel may be analyzed in an aqueous solution of salt by various instrumental techniques (See Nickel). Chloride ion in the aqueous solution may be determined by titration with silver nitrate using potassium chromate indicator or preferably by ion-chromatography. The solutions must be appropriately diluted for all analyses. [Pg.614]

Hydroxides Precipitation of hydroxides may be done through addition of a base to an aqueous solution of salts. Yttrium and copper hydroxides have a similar precipitation range but for the less polarizing Ba cation, very high pH is necessary to start the precipitation. However, two processes have been described that increase the pH of a solution of nitrates in water by addition of either NaOH (52) or tetramethyl ammonium hydroxide (53). It appears that at 60°C and... [Pg.304]

Skim milk can be considered as a two-phase system consisting of casein-colloidal calcium phosphate micelles in quasi-equilibrium with an aqueous solution of salts and proteins the phase boundary is ill-defined because of the intimate association between the calcium phosphate and the caseins (phosphoproteins). [Pg.161]

Thus, another difference between aqueous solutions of salts and organic solution is the fact, that, whereas in aqueous solution one may do well enough with the approximation that the cation is a charged sphere, and let its interaction with water be calculated on the basis of a simple charge field, in the organic phase it is essential to recognize a definite coordination... [Pg.58]

By treatment with sufficiently strong oxidising agents, such as chromic acid or potassium permanganate with hydrochloric or sulphuric acid, aqueous solutions of salts of basic tellurium are converted into solutions of telluric acid.17... [Pg.381]

Other matrices containing sufficient amounts of water (aqueous solutions of salts and alcohols) can also be expected to have trap structures of the types presented in Fig. 2. [Pg.163]

The salt monomer method was successfully applied to the preparation of the electrically-conducting polyimide-carbon black composites [62]. The composites are prepared as follows An aqueous solution of salt monomer 9PMA was mixed with carbon black, giving a suspension. This was evaporated to dryness under reduced pressure to afford a homogeneously-mixed powder composed of the salt monomer and carbon black. The powder was subjected to solid-state thermal polycondensation in the form of a pellet at 240 °C for 1 h under atmospheric pressure. The semiconducting aliphatic polyimides (P-9PM, Tm=315 °C) having electric conductivity of about 10"6 S/cm was readily obtained by mixing only 1 wt% of carbon black based on the polyimide. [Pg.18]

An aqueous solution of salt monomer 9PME was mixed with tetramethoxysi-lane, yielding a gel, which was then vacuum-dried forming a precursor powder composed of silica gel and the salt monomer. This was subjected to high-pressure polycondensation under 235 MPa at 230 °C for 5 h, producing polyimide-silica hybrid molding. By varying the ratio of tetramethoxysilane to the salt... [Pg.18]

The bifunctional zeolite catalysts are composed of both acid sites and metal clusters. The preparation methods of these catalysts encompasses three steps ion exchange, calcination, and reduction. The ion-exchange process is carried out with aqueous solutions of salts or, more commonly, of complexes of the metals that will be incorporated into the zeolite cavities and channels. [Pg.107]

The deposition of a thin layer of metal on an object by passing an electric current through an aqueous solution of salt containing ions of the element being deposited. [Pg.52]

The oxide Th02 is formed on heating the nitrate or the hydroxide. Addition of H2O2 to aqueous solutions of salts gives an insoluble peroxide of variable composition. [Pg.1142]


See other pages where Aqueous solutions of salts is mentioned: [Pg.164]    [Pg.249]    [Pg.366]    [Pg.738]    [Pg.199]    [Pg.495]    [Pg.659]    [Pg.323]    [Pg.224]    [Pg.273]    [Pg.512]    [Pg.524]    [Pg.524]    [Pg.525]    [Pg.103]    [Pg.249]    [Pg.652]    [Pg.233]    [Pg.519]    [Pg.27]    [Pg.425]    [Pg.489]    [Pg.74]    [Pg.193]    [Pg.692]    [Pg.254]    [Pg.286]    [Pg.945]   
See also in sourсe #XX -- [ Pg.254 , Pg.255 , Pg.256 , Pg.257 , Pg.258 , Pg.259 , Pg.260 ]

See also in sourсe #XX -- [ Pg.603 , Pg.604 , Pg.605 ]




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