Solvent:water ratios

Table 18.1.2 shows how the application of the various formulae affects the result of calculation. The VOC contents, calculated after ISO/DIS 11 890, are credible for Examples 2,3,4. Values calculated according to ASTM, using ratio solvent - water in Examples 2 and 4, are almost the same as VOC contents calculated according to ISO/DIS. 

The mole fraction x is the ratio of the niimher of moles of H9 in solution to the total moles of all constituents contained. To calculate the weights of H9 per 100 weights of H2O, one can use the following formula, where the siihscripts A and w correspond to the solute (hydrogen) and solvent (water) ... 

In the past few years, a range of solvation dynamics experiments have been demonstrated for reverse micellar systems. Reverse micelles form when a polar solvent is sequestered by surfactant molecules in a continuous nonpolar solvent. The interaction of the surfactant polar headgroups with the polar solvent can result in the formation of a well-defined solvent pool. Many different kinds of surfactants have been used to form reverse micelles. However, the structure and dynamics of reverse micelles created with Aerosol-OT (AOT) have been most frequently studied. AOT reverse micelles are monodisperse, spherical water droplets [32]. The micellar size is directly related to the water volume-to-surfactant surface area ratio defined as the molar ratio of water to AOT,... 

The reaction mass consists of two liquid phases and one solid phase no solvent is required. The major liquid phase is the crude amine product itself. The solid phase is promoted sponge nickel catalyst. Surrounding the catalyst is a second liquid phase consisting of concentrated caustic and water. Water and caustic are added continuously to make up for losses leaving in the crude product. The ratios of water, caustic, and catalyst in the reaction mass are controlled to produce high yields of product amine and very low catalyst usages. High catalyst concentrations are employed in the reaction mass to keep the concentration of unreacted nitriles very low the upper limit on the catalyst concentration is the point where the circulation rate is inhibited. 

In this equation, e is the actual potential and f° is the standard potential, n is the number of electrons involved, and Q is a ratio of concentration terms. Q is equal to the ratio of concentrations of products to concentrations of reactants, each raised to the power corresponding to the coefficient in the balanced chemical equation. Pure solids and liquids and the solvent water are not included in Q their effective concentrations are assumed to be 1. Gas pressures in atmospheres are used instead of concentrations. For a general reaction... 

The semi-empirical Yasuda-Shedlovsky technique of extrapolating a series of apparent pKa values obtained in several ratios of water/solvent to obtain an aqueous value is well established [32, 33], but three or more experiments are required and this adds significantly to assay times. A method of calculating aqueous pKas for various classes of organic acids and bases from single apparent pKa values obtained in water/solvent mixtures has been reported [34], and shows promise as a means of further speeding pKa measurement. 

Procedure If the fixed sample is studied, the cells are treated with tested allelochemical 10-5 - 10 4 M dissolved in organic solution (ethanol, chloroform, dimethylsulfoxide). But if the vital sample is needed, the solution is first diluted with water up to the ratio of organic solvent water, was more than 100. 

Kd = the solute s organic solvent water distribution coefficient. k = chromatographic capacity ratio (k — tr — t0/t0, tr and t0 being solute retention time and mobile phase holdup time, respectively), a and b = coefficients whose magnitudes depend on the LL distribution and RPLC systems. 

The isotopic abundance of deuterium in the L30+ ion will differ from that in the water with which it is equilibrated. This is expressed in terms of the fractionation factor / which is the ratio of D/H ratios in the lyonium ion and the mixed solvent (water)... 

Study of the effect of small amounts of water in the liquid, organic phase on the polymerization of bisphenol-A and HFB in several solvents.[14] Solvents were rigorously dried and assayed for water content by potentiometric Karl Fischer titration. A series of polymerizations catalyzed and uncatalyzed in each solvent were carried out in which the water content was increased incrementally. Polymer yields and inherent viscosities were determined as a function of water content in each solvent. The optimal water content expressed as the mole ratio of water to catalyst shows that the necessary water level varies substantially with solvent (see Table V and Figure 1-3). 

Specific acid-catalysed solvolysis of l-methoxy-l,4-dihydronaphthalene or 2-methoxy-l,2-dihydronaphthalene in 25% acetonitrile in water has been found to yield mainly the elimination product, naphthalene, along with a small amount of 2-hydroxy-1,2-dihydronaphthalene, there being no trace of either the 1-hydroxy-1,4-dihydronaphthalene or the rearranged ether. The nucleophilic selectivity, ns/ hoh = 2.1 X 10", between added azide ion and solvent water has been estimated for the relatively stable = 1 x 10 s ) intermediate benzallylic carbocation for which the barrier to dehydronation is unusually low k = 1.6 x 10 ° s ), as evidenced by the large elimination-to-substitution ratio with solvent water as base/nucleophile. The kinetics of acid-catalysed solvolysis of 1-hydroxy-1,4-dihydronaphthalene and 2-hydroxy-1,2-dihydronaphthalene have also been studied. 

The amount of water solubilized in a reverse micelle solution is commonly referred to as W, the molar ratio of water to surfactant, and this is also a good qualitative indicator of micelle size. This is an extremely important parameter since it will determine the number of surfactant molecules per micelle and is the main factor affecting micelle size. For an (AOT)/iso-octane/H20 system, the maximum Wq is around 60 [16], and above this value the transparent reverse micelle solution becomes a turbid emulsion, and phase separation may occur. The effect of salt type and concentration on water solubilization is important. Cations with a smaller hydration size, but the same ionic charge, result in less solubilization than cations with a large hydration size [17,18]. Micelle size depends on the salt type and concentration, solvent, surfactant type and concentration, and also temperature. 

Table 6.2 presents data showing the effect of various CMOS on the activity coefficient or mole fraction solubility of naphthalene, for two different solvent/water ratios. To examine the cosolvent effect, Schwarzenbach et al. (2003) compare the Hildebrand solubility parameter (defined as the square root of the ratio of the enthalpy of vaporization and the molar volume of the liquid), which is a measure of the cohesive forces of the molecule in pure solvent. 

The distribution ratios obtained were compared to the corresponding distribution ratios between water and Toctanol. The authors also calculated solvent parameters of [C4Cilm][PFg] (Section 9.3). It was shown that phenolate-ion associates with [C4CiIm][PFg] more strongly than other ions. The authors also mention the possibility of extraction of amino acids into [C4CiIm][PPg] in the presence of crown ether dibenzo-18-crown-6, though at rather moderate efficiency. 

In the case of the solvent (water, concentration = 55.5 mol dm-3), its standard activity is usually taken to be 1. For solvents, the definition of activity is the ratio of its vapour pressure when acting as a solvent, p, divided by the vapour pressure of the pure solvent, p°, taken as the standard state ... 

The intrinsic viscosity of poly(L-proline) is studied as a function of molecular weight and temperature In five commonly used solvents water, trifluoroethanol, acetic acid, propionic acid, and benzyl alcohol. The characteristic ratio is 14 in water and 18-20 in the organic solvents at 303 K, and d (in 0) / d T is negative. The theoretical rotational potential function obtained by Hopfinger and Walton for u-prolyl-L-prolyl-t-prolyl-t-proline J. Macromol. Scl. Phys. 1969, 3, 171 correctly predicts the characteristic ratio at 303 K but predicts the wrong sign for tfiln < >0) IdT. 

For mixtures of organic solvents with water, the available information (2) is derived only from reactions involving dissociation of hydrogen ion, leading to acidity function H. Measurements for solutions containing a constant concentration of a base and a varying ratio of water and the organic solvent were... 

---