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Total analytical concentration

Partition ratios, K the ratio of total analytical concentration of a solute in the stationary phase, CS, to its concentration in the mobile phase, CM. [Pg.335]

Distribution ratio is the total analytical concentration of a substance in the organic phase to its total analytical concentration in the aqueous phase, usually measured at equilibrium. Symbol D. D shall be defined and, preferably, specified by an index if the distribution of mercury is measured, the distribution ratio is written D(Hg) or The term partition ratio is not used for the distribution ratio. [Pg.717]

The set of partial differential equations developed for the simultaneous transfer of moisture, hear, and reactive chemicals under saturated/unsaturated soil conditions has been solved by the Galerkin finite element method. The chemical transport equations are formulated in terms of the total analytical concentration of each component species, and can be solved sequentially (Wu and Chieng, 1995). [Pg.219]

The use of antibodies has allowed the development of a technique known as immunodiagnostics, especially attractive for the direct analysis of intrinsically complex samples such as blood, serum, urine, food, etc. An immunoassay is a test that uses antibody-antigen complexes as a means of generating a measurable result. The specific interaction between epitopes and paratopes lies at the heart of every immunoassay. The role of antibodies in immunoassays is based on the observation that, in a system containing the determinant and a specific antibody, the distribution of the former between its antibody-bound and antibody-free forms is quantitatively related to the total analyte concentration. [Pg.112]

There are several ways to represent the dose-response curves in MIP ILAs. Plots of l/B vs 7. Bq/B s /. /T /Sq vs /. and F /B vs / , where Tis the (total) analyte concentration, etc., can be represented and fitted to two different models, namely the mechanistic (or theoretical, based on assay theory) or the empirical based on the mathematical fitting of the measured responses [41]. [Pg.131]

IUPAC recommendations for defining D are [7] distribution coefficient, D the ratio of the total (analytical) amount of a solute per gram of dry ion exchanger to its analytical concentration (total amount per cm ) in the solution concentration distribution ratio, D the ratio of the total (analytical) concentration of a solute in the ion exchanger to its concentration in the external solution (dimensionless) the concentrations are calculated per cm of the swollen ion exchanger and cm of the external solution volume distribution coefficient, D, the ratio of the total (analytical) concentration of a solute in the ion exchanger calculated per cm of the column or bed volume to its concentration (total amount per cm ) in the external solution. [Pg.383]

The solute may be present in solution in several dififerent chemical forms. Of more practical interest is the distribution of the total analytical concentration of a substance in the two phases. A distribution ratio D of a solute A is defined by D = where Ca , is th analytical concentration in the organic phase and... [Pg.428]

In Beer s law, c is the total analytical concentration of the absorbing species in a particular molecular... [Pg.3461]

At pH values around 6 yn 7.5, the inorganic phosphate (pXa = 6.82) exists as a mixture of HO-POsH and HO-PO forms. Similarly, the terminal phosphates of ATP (pKa = 6.95) and ADP (pS — 6.68) exist as mixtures of the mononegative and dinegative ions. It would be much simpler to define in terms of total [ATP], [ADP], and [P ]- bet us return to our esterase reaction in order to see how total analytical concentrations are incorporated into the Xiq and AG expressions. We would like to determine the value for KL, where ... [Pg.157]

Notice that the two curves cross at the point where pH = pKhqac 4.74. At this point, the concentrations of acetic acid and acetate ion are equal, and the fractions of the total analytical concentration of acid both equal one half. [Pg.257]

We can draw a logarithmic concentration diagram easily by noting the relationships just given. An easier method is to modify the distribution diagram so that it produces the logarithmic concentration diagram. This is the method illustrated in Applications of Microsoft Excel in Analytical Chemistry , Chapter 8. Note that the plot is specific for a total analytical concentration of 0.10 M and for maleic acid, since the acid dis.sociation constants are included. [Pg.423]

In many experimental situations, one controls the total analytical concentration, C, i.e., the sum of the concentrations of the various possible forms present. For example, we may weigh a certain amount of acetic acid and/or sodium acetate, and dissolve it in a given amount of water, in which case we know the total analytical concentration C = [HAc] + [Ac ]. In situations like that it is often useful to define the concentration fraction of a particular species in the mixture. For the simple monoprotic acid defined in (4.1-3) we have... [Pg.122]

Imagine being asked to calculate the pH of a 0.1 M solution of acetic acid in water. What principles would you use to find the answer to such a question, and how would you go about it Obviously, the pH will depend on how much acid is used (0.1 M), and on the strength of the particular acid, i.e., on the total analytical concentration C and the dissociation constant Ka. Here is how these numbers can be used to arrive at the answer. [Pg.127]

The buffer strength of a triprotic acid, as a function of its total analytical concentration and of pff, is given by... [Pg.153]

A more practical parameter is the distribution coefficient D, which gives the corresponding ratio of the total analytical concentrations,... [Pg.183]

Finally, the solubility SHg of mercury is defined as the total analytical concentration of all mercury species in the saturated solution. Assuming that the concentration of dissolved HgS is negligible, we have... [Pg.187]

How do we represent the solution when a precipitate can form or dissolve We need one piece of additional information, namely the total analytical concentration of silver when all precipitate is dissolved. (This depends both on the amount of precipitate and on the volume of solution, but we only need the resulting analytical concentration in the absence of precipitate.)... [Pg.191]

Consider, for example, the redox equilibrium Fe3++ e = I e2. When we define the total analytical concentration of iron in solution (regardless of its oxidation state) as C, it follows from the Nernst equation that the fractional concentrations of Fe3+and Fe2+are... [Pg.205]

All redox titration curves we have discussed here are independent of the total analytical concentration C of the redox couple. (This is not always the case in the Cr2072 / Cr 3+couple the reduction of one Cr2072- generates two Cr3+ions, which leads to a concentration-dependent redox titration curve.) Therefore, the above expressions precisely give Cs/ln (10) times the first derivative of the progress curve of the corresponding redox titration. You can convince yourself that this is so in exercise 5.10-1. [Pg.218]

Table 6.1-1 The total analytical concentration Cof 2,4-dinitrophenol in water, and the resulting concentration [A-] of2,4-dinitrophenolateas measured by differential spectrometry. Table 6.1-1 The total analytical concentration Cof 2,4-dinitrophenol in water, and the resulting concentration [A-] of2,4-dinitrophenolateas measured by differential spectrometry.
Solution chemistry. Note that C, in the surface complexation model formulation is the free ion concentration, while in the Langmuir isotherm it is the total analytical concentration. In reality, the formation of aqueous complexes will change the surface adsorption (affecting the term C,). The speciation of i may also change with time. [Pg.204]

The initial conditions for the transport model were the total analytical concentrations of components estimated from the complete digestions of tailings samples. Four tailings piles exist at the site and will be filled in the repository Carbonate, Vanadium, Acid and East Piles. The Vanadium Pile contains pore fluids with pH values from 7 to 13 and... [Pg.226]


See other pages where Total analytical concentration is mentioned: [Pg.121]    [Pg.12]    [Pg.87]    [Pg.154]    [Pg.435]    [Pg.26]    [Pg.361]    [Pg.31]    [Pg.65]    [Pg.850]    [Pg.121]    [Pg.199]    [Pg.502]    [Pg.354]    [Pg.156]    [Pg.157]    [Pg.159]    [Pg.150]    [Pg.503]    [Pg.124]    [Pg.146]    [Pg.180]    [Pg.193]    [Pg.217]    [Pg.231]    [Pg.233]    [Pg.233]   
See also in sourсe #XX -- [ Pg.122 ]




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