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Salt measurement

The transition took a course independent of concentration, reversible and extraordinarily fast. Transition temperature and kinetics were independent of pH and of the concentration of the salt. Measurements have been made either in acetic acid, (pH 3.0) or in 50 mM phosphate buffer at pH 7.5. [Pg.183]

Matsubayashi et al. revealed donor abilities of the unsymmetrical diimine-dithiolene complexes [11-14]. The unsymmetrical complexes provided cation radical salts with various anions including I3, Br3 and TCNQ by use of chemical oxidation [11-14]. The electrical resistivities of the cation radical salts measured with their compressed pellets at room temperature are summarized in Table 1. The electrical resistivities of the dmit complexes were very high. The cation radical salts of the CgH4Sg-complexes, which have the BEDT-TTF moiety [22, 23], exhibited lower resistivity than those of dmit complexes, except for [(Bu-pia)Pt(CgH4Sg)] salts. However, crystal structures of these salts were not reported, and details of their electrical properties and electronic states were not discussed based on their crystal structures. [Pg.41]

Warburg on the other hand used the theory of the concentration cell to relate the thermodynamic potential fx, of the mercurous salt, measured in ergs per grm. equivalent with V, the excess of the electric potential of the mercury over that of the dilute acid con-. taining the salt, expressed in volts thus ... [Pg.208]

S)-hydroxyacetic-2-d acid lithium salt measurement of Bijvoet 84... [Pg.394]

Salt Measured M—X spacing in vapor", A d 7/subb kcal/mole Crystal lattice energy, UQ, kcal/mole (U-JH), kcal/mole Comp. M+—X-distance in vapor, A... [Pg.66]

High-level waste canister motions in salt have been calculated for the various conditions which could be encountered in salt (5). Using the mechanical properties of salt measured as a function of temperature and assuming ten-year old waste with an initial thermal output of 3.5 kilowatts per canister, the calculated total motion of the canister is less than one meter relative to the surrounding salt. [Pg.31]

Figure 9 Long-range coupling constants (absolute values) and chemical shifts (p.p.m.) for thienothiapyrylium salts (measured in CF3C02D) values of electron densities in parentheses (calculated after the HMO method with h = 0.9, kc-s 0.9)... Figure 9 Long-range coupling constants (absolute values) and chemical shifts (p.p.m.) for thienothiapyrylium salts (measured in CF3C02D) values of electron densities in parentheses (calculated after the HMO method with h = 0.9, kc-s 0.9)...
The specific conductance/conductivity k (S/cm) of salts measured by a conductivity detector is given by... [Pg.433]

The common commercial or laboratory alkanesul-fonamides are listed in Table 6. Of these, methane-sulfonamide, A-methyl methanesulfonamide, A-butyl benzenesulfonamide, and trifluoromethanesulfonimide are in commercial production, the latter in the form of its lithium salt. Measured values are available for a variety of aromatic and akanesulfonamides and sulfonamides along with a discussion on substituent effects. ... [Pg.3105]

Unlike most other salts, measurement of mixing enthalpies of molten alkali metal carbonates, due to their corrosive nature, cannot be performed in fused silica containers and be mixed by the usual break-off technique. Andersen and Kleppa (1976) showed that the Au20Pd alloy was corroded only negligibly by alkali metal carbonate melts kept under a relatively high CO2 pressure. The experimental arrangement included plunger as well as a dipper crucible that could be manipulated from the outer side of the furnace. The mass loss of the most volatile carbonate, Rb2C03, was about 0.3%. However, in spite of the relatively small vaporization losses, the attack of vapors on the fused silica liner was considerable and the lower part of the device had to be discarded after 10-15 experiments. [Pg.248]

The Macinnes convention leads to = Tci = 7 kci, We can now compute individual ion activity coefficients from their mean values measured in solutions of strong electrolytes using y Kci values as our starting point. (In the ideal strong electrolyte, cations and anions are unassociated with each other and thus do not form complexes [see Chap. 3].) It is important to remember that all such calculations must be done with y values for KCl and other salts measured at the same ionic strength, which is not the same molality except for monovalent-monovalent salts. [Pg.126]

Some of the same chemicals used to stiffen fabrics can also be used to increase a fabric s weight, an important sales specification. Silk fabrics can be conveniently weighted by the application of tin salts. Measurement of the degree of weighting can be done by comparing the final weight of the fabric in g m - to the initial weight. [Pg.121]

To represent a given system consisting of atB, yC, and zD in a given amount of water (where B, C, and D represent equivalent molecular amounts of the salts), measure off on OB and OC lengths Or and Oh equal to x and y respectively. From the points b and c lines ha and ca are drawn parallel to OB and OC. The point of intersection a (Fig. 146) then represents a solution containing xB and yC ah x ac y). From a a line dP is drawn parallel to OD and equal to z, P then represents the solution of the above composition. [Pg.282]

Figure 7. Small-angle neutron scattering curve of the quenched and unquenched Na salt. Measurements done at room temperature. Figure 7. Small-angle neutron scattering curve of the quenched and unquenched Na salt. Measurements done at room temperature.
The salt analysis consisted of soaking the reference sample in deionised water for 8h, to redissolve all the salt, then determining the salt concentration in the deionised water by titration with silver nitrate (0-0.5 molar) using an Orion EA940 expandable ion analyser link to a single junction reference electrode. Reproducibility of the salt measurement using this equipment was 0.001 mg/cm2. [Pg.330]

Directions (a) Grind in a mortar to a fine powder about 11 grams of potassium nitrate. (1) Weigh on a piece of paper on the platform scales 10.1 grams of the powdered salt. Measure into a 500 c.c. beaker 250 c.c. of water at room temperature and (2) read the temperature of the water to 0.1 degree. Pour the potassium nitrate into the water and stir with the thermometer. The salt should dissolve in less than 30 seconds. (3) Read the temperature when the salt has dissolved. [Pg.227]

Figure 8.11. Real and imaginary parts of the dielectric function, Ei and 2 of 4x-stretched emeraldine salt measured in the elongation direction. Reprinted from Mac Call et at., Phys. Rev. B, SO, 8, 5094 (1994). Copyright 1994 American Physical Society. Figure 8.11. Real and imaginary parts of the dielectric function, Ei and 2 of 4x-stretched emeraldine salt measured in the elongation direction. Reprinted from Mac Call et at., Phys. Rev. B, SO, 8, 5094 (1994). Copyright 1994 American Physical Society.
These observations differ from those of Frosh, who has reported that serum bile salt concentrations remain elevated after bilirubin concentrations and enzyme activities return to normal and who thus regards serum bile salt measurements as superior to other tests in revealing abnormalities in hepatitis (51). [Pg.69]

Fig. 16. Electrophoretic velocity of Na agar in dependence on the concentration of added salts (measurements on suspended Si02 particles). Fig. 16. Electrophoretic velocity of Na agar in dependence on the concentration of added salts (measurements on suspended Si02 particles).
This is enough to meet the world s demand for salt for seven or eight weeks. Since the seas contain about 1.35 billion cubic kilometers, the present rate of use would consume their chloride in about 180 million years. Solid deposits of salt, measured only in the billions of tons, add very little to this. Since over the course of 180 million years, a very high percentage of the chloride used will have found its way back to the seas, this situation is less alarming than it might appear. [Pg.466]

The conductivity values of the PAM salts measured as pellets are given in Table 4.12. The conductivity of the PAM salts are in the range of 0.3-0.9 S/cm. The higher conductivity of PAM obtained by the inverted emulsion method could be due to a more homogenous protonation of the imine nitrogen and a more ordered chain conformation of the polymer. The conductivity of the PAM-camphor sulfonic acid was found to be higher than the other salts (see Table 4.12). [Pg.112]

Note Gas matrix measurements are indicated by gm, aqueous measurements by aq, gas phase measurements by g, solid phase measurement by s and molten salt measurements by ms-References Kashiwabara et al. 1973 Akesson et al 1994 Strombeig et al. 1991 Loewenschuss et al. 1969 Sandstrom 1978 Biscarini et al. 1977 Bentham et al. 1985 Janz and James 1%3... [Pg.289]

Salt measurements on the samples showed that the samples had a salt content between 0.3 and 0.4%. When salt was added by salt injection the salt content of the wild post rigor group increased to 0.6% NaCl, but no significant change was found in the salt content for salt injected farmed or wild pre rigor samples. This indicated that only the wild post rigor muscle had an effective salt uptake in the study. [Pg.234]

Another technique, the isopiestic method, is appheable to systems eontaining only one volatile eomponent e.g. such as systems with salt). Measurement is easy but it needs a rather long time for achieving equihbrium. For more details we refer to the basic surveys given in Chap. 1.8. [Pg.19]

Table 6.42. chemical shifts of iminium, amidinium and guanidinium salts measured at 9.118 MHz, 301 K and originally referenced to NaNO, 2 (conversion factor = -1.5 ppm) 0.08m Cr(acac) was added to the solutions. (R13)... [Pg.159]


See other pages where Salt measurement is mentioned: [Pg.205]    [Pg.42]    [Pg.86]    [Pg.183]    [Pg.2]    [Pg.251]    [Pg.701]    [Pg.61]    [Pg.182]    [Pg.920]    [Pg.66]    [Pg.701]    [Pg.38]    [Pg.387]    [Pg.42]    [Pg.220]    [Pg.145]    [Pg.112]    [Pg.362]    [Pg.262]    [Pg.81]   
See also in sourсe #XX -- [ Pg.166 ]




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