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Water values

This table gives values of pKw on a molal scale, where Kw is the ionic activity product constant of water. Values are from W. L. Marshall and E. U. Franck, 7. Phys. Chem. Ref. Data, 10 295 (1981). [Pg.833]

Karl Fischer titration. This titration procedure determines the concentration of water present in AOS samples containing 40-70 wt % water. In Karl Fischer titrations, each equivalent of base interferes as 18 g of water. Since AOS samples are basic, water values obtained must be corrected for side reactions of reagent with alkaline material. Alkalinity must be determined to correct for this error. [Pg.452]

There are, however, at least four aspects of 5 0 variation in the biosphere which can affect this correlation and, as such, could account for the variation in the data. The two predictive models differ in the emphasis placed on each of these aspects. First, animal 8 0 values are not expected to vaiy predictably with rainfall and surface water in cases where animals obtain the majority of their body water from plants and where plant values vary independently of surface water values. For example, within Australia there is little continental variation in rainfall 5 0 values and little surface water for... [Pg.121]

SD and S O. 8D and of the ore fluids responsible for epithermal Au-Ag and base-metal vein-type deposits in Japan have been estimated from analyses of fluid inclusions (Hattori and Sakai, 1979) and minerals (Watanabe et al., 1976). These data are shown in Fig. 1.103. 8D values of ore fluids for epithermal Au-Ag vein-type deposits are similar to those of present-day meteoric water values. 8D values of epithermal ore fluids for base-metal vein-type deposits are slightly higher than those of epithermal Au-Ag vein-type deposits. This may be due to the boiling of epithermal base-metal ore fluids and involvement of seawater. [Pg.143]

SD and 8 0 values for epithermal deposits from other countries are summarized in Fig. 1.105 (Field and Fifarek, 1985). The oxygen shift away from the meteoric water line is always observed, but 8D is similar to meteoric water value, suggesting meteoric water source of epithermal ore fluids. Magmatic contribution to ore fluids has not been found except in some ore fluids responsible for the deposits in the other countries Tui... [Pg.144]

Oxygen isotopic fractionation factors used for the calculation were taken from Taylor (1997). Initial 8 0 value of hydrothermal solution (0%o) was estimated from 8 0 values of K-feldspar and quartz in the veins and homogenization temperatures (Shikazono and Nagayama, 1993), and that of groundwater (—7%c) was estimated from meteoric water value of the south Kyushu district (—7%c) (Matsubaya et al., 1975). [Pg.190]

The diffusion constant of water is consistent with the bulk water value for milk, however, it is slightly reduced in the cream sample and significantly reduced in the... [Pg.177]

As BH dissociates into H+ and the uncharged base B, the dielectric constant can exert only a minor effect on the mutual coulombic attraction, so that even in water (e = 78.5) the pKa values of aliphatic amines do not differ much from the above picture of the influence of solvent basicity. That piiTa(water) lies between ptfa(m.cresoi) and p a(acetlc acid) instead of between the latter and p.Ka(pyridine) may be ascribed to effects of solvation however, the p a(Water) values of the aromatic amines are low owing to effects of mesomerism. [Pg.291]

Transfer rate constants are postulated as shown in Table II, following the approach described by Mackay and Paterson (4). The air-water value selected was lower than is generally used since it appears that a low value is necessary to reconcile observed air and water concentration, and mass balances as discussed in a recent review of PCB behavior in the Great Lakes (Mackay et al. U3)). [Pg.185]

The two solvents most commonly used in microwave heating are ethanol and water. Values for water are given by Kaatze [13] and those for ethanol by Chahine et al. [14]. Water is dose to case 1 because both values decrease with temperature. In contrast, for ethanol the real part increases and the dielectric loss reaches a maximum at 45 °C (case 2). For ethanol, in fact, the working frequency is higher than relaxation frequency at room temperature. Ethanol has a single relaxation frequency, close to 1 GHz at 25 °C, and, furthermore, its relaxation frequency increases fairly rapidly with temperature (3 GHz at 65 °C). For water the working frequency is smaller than the relaxation frequency at all temperature (17 GHz at 20 °C and 53 GHz at 80 °C). [Pg.14]

We start by looking up the enthalpies of formation A//f for ethene, ethanol and water. Values are readily found in books of data Table 3.1 contains a suitable selection. [Pg.118]

Thus, errors in all the heats, apart from the precisely known water value, are decreased ra-fold in the required heat. The hydrolysis heat A//2 is always much less than At and can be measured less precisely. The reactions involved in reactions 2, 3, and 6 of Table II have been used in the CODATA evaluation of Aif,(F q)), although in theorv reactions 7 and 8 should lead to more accurate values. In practice this may not be true. Thus the fluorination of iodine produces some IF7, together with the bulk of IF5, and errors in estimating the mixture can cause uncertainty in the final value of AZf/IF ). The hydrolysis heat for the reaction... [Pg.16]

Enthalpies of solution of anhydrous rare-earth chlorides in nonhy-droxylic solvents are also scant. What values exist are collected together in Table XII (178, 183, 218, 220-222), which includes alcohol and water values for ease of comparison. The values in this table are direct calorimetric measurements, performed on anhydrous trichlorides. The value for gadolinium trichloride in dimethylformamide is... [Pg.90]

It is also possible to measure surface area from the water adsorption isotherm, and this is arguably more relevant to aqueous pulp suspensions as it measures the surface area which is accessible to water. Values of up to 140 m2g-1 have been obtained from the... [Pg.73]

Chemical composition for different synthetic marine waters. Values are expressed as g L 1... [Pg.865]

Experiments on the hydrolysis of 4-(p-chlorophenoxy) butyl bromide, (PCBB) which proceeds via an Sj 2 substitution mechanism (11) were similar in design and data analysis procedures to the chlorpyrifos experiments detailed above. Results from a study at 35°C using EPA-12 sediment with 80% of the compound in the sorbed state are illustrated in Figure 5. Calculated and observed values from this study, using the distilled water value for of (7.9 0.5xl0 ) min a... [Pg.234]

The recent work of Wang and Lien (29) illustrates that ion-pair partitioning occurs to a greater extent than previously realized. Partition coefficients calculated from measurements made on partially ionized compounds depend not only on the pH, but on the buffer used. They may vary by more than one log unit. The authors derived equations to correct log P to octanol/water values, but these can still be off by several tenths of a log unit. A preferable solution would be to know the log Pj and account for ion-pair partitioning. [Pg.242]

Fig. 3.41 Predicted (bars) and measured (crosses) oxygen isotope composition of separated minerals from Haitian weathering profiles. The ranges of predicted values were calculated assuming a temperature of 25°C and a meteoric water value of —3. %o (after Bird et al. 1992)... Fig. 3.41 Predicted (bars) and measured (crosses) oxygen isotope composition of separated minerals from Haitian weathering profiles. The ranges of predicted values were calculated assuming a temperature of 25°C and a meteoric water value of —3. %o (after Bird et al. 1992)...
Experimental and Estimated log P0ct/water Values for a Set of 49 Acetylated Amino Acids and Dipeptides... [Pg.229]


See other pages where Water values is mentioned: [Pg.486]    [Pg.353]    [Pg.205]    [Pg.15]    [Pg.61]    [Pg.493]    [Pg.194]    [Pg.194]    [Pg.76]    [Pg.177]    [Pg.122]    [Pg.132]    [Pg.134]    [Pg.143]    [Pg.559]    [Pg.598]    [Pg.24]    [Pg.30]    [Pg.154]    [Pg.161]    [Pg.169]    [Pg.176]    [Pg.108]    [Pg.117]    [Pg.1121]    [Pg.57]    [Pg.323]    [Pg.80]    [Pg.234]    [Pg.485]    [Pg.161]   
See also in sourсe #XX -- [ Pg.309 ]

See also in sourсe #XX -- [ Pg.14 , Pg.82 , Pg.147 ]

See also in sourсe #XX -- [ Pg.224 , Pg.228 ]




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