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Solubilities of substances

Adequate precaution and care must be exercised in determining partition coefficients based on the solubility data as S, is not the solubility of substance A in pure Solvent a , but rather the solubility in Solvent a saturated with Solvent cb ... [Pg.394]

The solubility of substances in SCFs has been described by many different approaches [41-43]. Based on experimental data, theoretical treatment allows for modeling the solubility in SCCO2 [44,45]. Other approaches are based on equations of state (EOS) or on statistic models [46,47]. [Pg.116]

Find the mass of potassium dichromate that saturates 100 g of water, 100 g of solution, and 1000 ml of solution at the noted temperature. How can the solubility of substance be expressed ... [Pg.77]

This limitation causes the temperature-limits for the solubility of the initial and end products of the reaction. Normally, at higher pressure levels an increase in temperature also results in higher solubilities of substances in supercritical fluids because the increase in the vapour-pressure of the compounds to be dissolved overcomes the reduction in density. [Pg.488]

They mainly dissolve in water. This is because water molecules are able to bond with both the positive and the negative ions, which breaks up the lattice and keeps the ions apart. Figure 3.17 shows the interaction between water molecules (the solvent) and sodium and chloride ions from sodium chloride (the solute). For a further discussion of the solubility of substances see Chapter 8 (p. 129). [Pg.53]

Generally, they do not dissolve in water. However, water is an excellent solvent and can interact with and dissolve some covalent molecules better than others. Covalent substances are generally soluble in organic solvents. For a further discussion of solubility of substances in organic solvents see Chapters 14 and 15. [Pg.61]

The solubility of substances such as carboxylic acids, which dissociate or form ions in solution, is also a function of pH, a common environmental example being pentachlo-rophenol. Data must thus be at a specified pH. Alternatively, the solubility of the parent (non-ionic) form may be given, and pKa or pKb given, to permit the ratio of ionic to nonionic forms to be calculated as... [Pg.148]

The general rules of solubility help us to predict whether or not a substance is soluble in water. If 1 g of a substance can dissolve in water to make 100 g of solution, we say that the substance is soluble. If less than 1 g but more than 0.1 g can dissolve, the substance is slightly soluble. If a substance can only dissolve in water if less than 0.1 g is present, we say that the substance is insoluble. These criteria for solubility of substances are determined at 25°C. The following rules summarize the solubility of a large number of substances ... [Pg.309]

The solubility of substances in different solvents is determined by the relation between the attraction forces among the molecules of that substance and the attraction forces that occur between the molecules of the solvent. If the two are similar in strength and in kind, solubility... [Pg.236]

Many interrelated factors affect the solubility of substances in water. This makes it challenging to predict which ionic substances will dissolve in water. By performing experiments, chemists have developed guidelines to help them make predictions about solubility. In Investigation 9-A, you will perform your own experiments to develop quidelines about the solubility of ionic compounds in water. [Pg.331]

For ideal solutions Van 5t Hoff s law holds for the solubility of substance B ... [Pg.365]

Liquid Xenon is a low-temperature solvent for the temperature range between -112 °C mp, p bar) and 17 °C scp,p 60 bar). The greatest advantage of this unusual solvent is its complete transparency over the IR spectral range. The limited solubility of substances in liquid xenon is often compensated by a longer optical pathway of the cell [1]. Because of the inertness of LXe and the weak interactions between LXe and the dissolved species the method allows a kind of "low temperature gas phase spectroscopy". [Pg.838]

Of Indirect interest are books on solubilities because the solubility of substances contributes to determining their tendencies to adsorb. [Pg.242]

The basis for the relationship between bioconcentration and log Kow is the analogy for the partition process between the lipid phase of fish and water and the partition process between n-octanol and water. The reason for using K w arises from the ability of octanol to act as a satisfactory surrogate for lipids in fish tissue. Highly significant relationships between log Kow and the solubility of substances in cod liver oil and triolin exist (Niimi, 1991). Triolin is one of the most abundant triacylglycerols found in freshwater fish lipids (Henderson and Tocher, 1987). [Pg.504]

Liquid-like densities of supercritical gases result in liquid-like solvent powers this property and faster diffusion characteristics due to low-gas viscosity make supercritical fluids attractive extraction agents. Solubility of substances in supercritical gases derives from van der Waals molecular attractive forces and increases with increasing pressure at a constant temperature. The temperature influences the solution equilibria in a more complicated way than does the pressure. Compounds can be selectively dissolved by changing the density of the gas, i.e., pressure and temperature conditions. [Pg.663]

The solubilities of ionic salts have wide range. For instance, in contrast to silver perchlorate (AgC104), which has a solubility of 55.7 g per 100 g of water, only 0.00018 g of silver chloride (AgCl) can dissolve in 100 g of water. If the maximum amount of solute dissolved in 100 g of water is less than 0.1 g, this solute is said to be insoluble. The solute that has a solubility range from 0.1 g to 1 g is called slightly soluble. If the amount of solute is more than 1 g, then it is soluble. Silver perchlorate is a soluble compound but silver chloride is an insoluble compound in water. It is not necessary to memorize the solubilities of substances. Solubility tables (e.g.,Table 2) help you determine whether a substance is soluble, insoluble, or slightly soluble in water. [Pg.21]

The solubilities of substances do not depend only on the amount of solute or solvent. Temperature and pressure are also factors that affect solubility. As for stirring, even if it seems to increase solubility, it actually has no effect. Stirring only speeds up dissolution. [Pg.22]

Subsequently the use of entrainers is restricted to rare and specific applications mainly to enhance the solubility of substances on the lower edge of extractability. [Pg.54]

When the relative hydrophobicity of solutes is estimated by the partitioning in the solvent system, one is faced with the aforementioned problem arising when measuring the comparative solubility of substances in water and in an organic solvent, that is which solvent should be used to simulate a nonpolar medium. [Pg.181]

Solubility of Substances in Various Solid-State Forms... [Pg.17]

We start this stage of our exploration of the nature of solutions by looking at some of the reasons why certain substances mix to form solutions and why others do not. When you are finished reading this section, you will have the necessary tools for predicting the solubility of substances in liquids. [Pg.574]

A substance in solution has a chemical potential, which is the partial molar free energy of the substance, which determines its reactivity. At constant pressure and temperature, reactivity is given by the thermodynamic activity of the substance for a so-called ideal system, this equals the mole fraction. Most food systems are nonideal, and then activity equals mole fraction times an activity coefficient, which may markedly deviate from unity. In many dilute solutions, the solute behaves as if the system were ideal. For such ideally dilute systems, simple relations exist for the solubility of substances, partitioning over phases, and the so-called colligative properties (lowering of vapor pressure, boiling point elevation, freezing point depression, osmotic pressure). [Pg.63]

The Le Chatelier-Shreder equation presents the thermal dependence of the liquidus in the pre-eutectic region of the phase diagram with the simple eutectic. The same equation expresses the thermal dependence of the solubility of substance B in the solvent A . This equation allows us to draw some conclusions concerned with the interactions in eutectic systems, and the behaviour of the substance s solubility during variation of the solution temperature. The most general of these conclusions are as follows ... [Pg.296]

Figure 7,6 shows the solubilities of quartz and amorphous silica in relation to the minerals of Fig. 7.5. The solubilities of substances having the empirical formula SiC>2 or SiC>2 /1H2O have been studied for decades. These studies are much more complicated than they appear, because of the reluctance of soluble silica to reach equilibrium or even metastable equilibrium with its solid phases. Soluble silica tends to polymerize slowly in supersaturated solutions rather than to precipitate cleanly. In addition, the solid phase that precipitates is often amorphous silica instead of the most stable phase, quartz or its close relative chert. Amorphous silica is metastable and much more soluble than quartz. The solubilities of amorphous silica and quartz are often assumed to be the upper and lower limits of silica solubility in soils. Viewed from the range of soil solution compositions shown in Fig. 7.6, silica concentrations caii be less than the equilibrium solubility of quartz even though quartz is almost always present in the sand fraction of soils. The slow kinetics of silica reactions and the slow release of Si(OH)4 during weathering create wide deviations from equilibrium. Figure 7,6 shows the solubilities of quartz and amorphous silica in relation to the minerals of Fig. 7.5. The solubilities of substances having the empirical formula SiC>2 or SiC>2 /1H2O have been studied for decades. These studies are much more complicated than they appear, because of the reluctance of soluble silica to reach equilibrium or even metastable equilibrium with its solid phases. Soluble silica tends to polymerize slowly in supersaturated solutions rather than to precipitate cleanly. In addition, the solid phase that precipitates is often amorphous silica instead of the most stable phase, quartz or its close relative chert. Amorphous silica is metastable and much more soluble than quartz. The solubilities of amorphous silica and quartz are often assumed to be the upper and lower limits of silica solubility in soils. Viewed from the range of soil solution compositions shown in Fig. 7.6, silica concentrations caii be less than the equilibrium solubility of quartz even though quartz is almost always present in the sand fraction of soils. The slow kinetics of silica reactions and the slow release of Si(OH)4 during weathering create wide deviations from equilibrium.
The nature of (he solvent and substance to be dissolved,—No rule con be given which will apply in a general way to the solvent power of liquids or Uie solubility of substances. Water is of all liquids the best solvent of most substances iu it some substances are so readily soluble that they absorb a sufficiency from the atmosphere to form a solution as calcium chloride. Such substances are said to be detiouescenl. Other substances... [Pg.103]

SAMPLE PROBLEM 13.1 Predicting Relative Solubilities of Substances Problem Predict which solvent will dissolve more of the given solute ... [Pg.394]

The solubility of substances in water is given in different terms, usually as g or mg of substance per 100 g or 1 litre of water. The dependence of the solubility of substances on temperature is expressed graphically by so-called solubility curves. Some of characteristic solubility curves are shown... [Pg.29]


See other pages where Solubilities of substances is mentioned: [Pg.447]    [Pg.25]    [Pg.106]    [Pg.394]    [Pg.42]    [Pg.488]    [Pg.519]    [Pg.120]    [Pg.285]    [Pg.674]    [Pg.55]    [Pg.189]    [Pg.2035]    [Pg.294]    [Pg.789]    [Pg.103]    [Pg.134]    [Pg.376]    [Pg.302]    [Pg.278]    [Pg.576]    [Pg.1437]    [Pg.29]   
See also in sourсe #XX -- [ Pg.83 , Pg.85 ]




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