Titratable acidity, definition

Typical values of pK[nt and pfor a humic acid are 2.67 and 4.46. The introduction of the electrostatic factor into the equilibrium constant is analogous to the coulombic term used in the definition of the intrinsic surface complexation constants. In addition another binding site (WAH) is recognised which is thought to behave as a weak acidic phenolic functional group. Although this site does not contribute to the titratable acidity and, therefore, no pK is needed for proton dissociation, it is involved in metal complexation reactions. The total number of the three monoprotic sites is estimated from titratable acidity and then paired to represent the humic substance as a discrete non-interacting mixture of three dipro-tic acids, which act as the metal complexation sites. The three sites are... 

The alkalinity is determined by titration of the sample with a standard acid (sulfuric or hydrochloric) to a definite pH. If the initial sample pH is >8.3, the titration curve has two inflection points reflecting the conversion of carbonate ion to bicarbonate ion and finally to carbonic acid (H2CO2). A sample with an initial pH <8.3 only exhibits one inflection point corresponding to conversion of bicarbonate to carbonic acid. Since most natural-water alkalinity is governed by the carbonate—bicarbonate ion equiUbria, the alkalinity titration is often used to estimate their concentrations. 

Buffers are solutions that tend to resist changes in their pH as acid or base is added. Typically, a buffer system is composed of a weak acid and its conjugate base. A solution of a weak acid that has a pH nearly equal to its by definition contains an amount of the conjugate base nearly equivalent to the weak acid. Note that in this region, the titration curve is relatively flat (Figure 2.15). Addition of H then has little effect because it is absorbed by the following reaction ... 

The last definition has widespread use in the volumetric analysis of solutions. If a fixed amount of reagent is present in a solution, it can be diluted to any desired normality by application of the general dilution formula V,N, = V N. Here, subscripts 1 and 2 refer to the initial solution and the final (diluted) solution, respectively V denotes the solution volume (in milliliters) and N the solution normality. The product VjN, expresses the amount of the reagent in gram-milliequivalents present in a volume V, ml of a solution of normality N,. Numerically, it represents the volume of a one normal (IN) solution chemically equivalent to the original solution of volume V, and of normality N,. The same equation V N, = V N is also applicable in a different context, in problems involving acid-base neutralization, oxidation-reduction, precipitation, or other types of titration reactions. The justification for this formula relies on the fact that substances always react in titrations, in chemically equivalent amounts. 

Brdnsted-Lowry theory, 194 contrast definitions, 194 indicators, 190 reactions, 188 titrations, 188 Acids, 183 aqueous, 179 carboxylic, 334 derivatives of organic, 337 equilibrium calculations, 192 experimental introduction, 183 names of common, 183 naming of organic, 339 properties of, 183 relative strengths, 192, 451 strength of, 190 summary, 185 weak, 190, 193 Actinides, 414 Actinium... 

A1C13, or S02 in an inert solvent cause colour changes in indicators similar to those produced by hydrochloric acid, and these changes are reversed by bases so that titrations can be carried out. Compounds of the type of BF3 are usually described as Lewis acids or electron acceptors. The Lewis bases (e.g. ammonia, pyridine) are virtually identical with the Bransted-Lowry bases. The great disadvantage of the Lewis definition of acids is that, unlike proton-transfer reactions, it is incapable of general quantitative treatment. 

Discussion. The hydroxides of sodium, potassium, and barium are generally employed for the preparation of solutions of standard alkalis they are water-soluble strong bases. Solutions made from aqueous ammonia are undesirable, because they tend to lose ammonia, especially if the concentration exceeds 0.5M moreover, it is a weak base, and difficulties arise in titrations with weak acids (compare Section 10.15). Sodium hydroxide is most commonly used because of its cheapness. None of these solid hydroxides can be obtained pure, so that a standard solution cannot be prepared by dissolving a known weight in a definite volume of water. Both sodium hydroxide and potassium hydroxide are extremely hygroscopic a certain amount of alkali carbonate and water are always present. Exact results cannot be obtained in the presence of carbonate with some indicators, and it is therefore necessary to discuss methods for the preparation of carbonate-free alkali solutions. For many purposes sodium hydroxide (which contains 1-2 per cent of sodium carbonate) is sufficiently pure. 

The standard solution is prepared by dissolving a weighed amount of pure potassium iodate in a solution containing a slight excess of pure potassium iodide, and diluting to a definite volume. This solution has two important uses. The first is as a source of a known quantity of iodine in titrations [compare Section 10.115(A)] it must be added to a solution containing strong acid it cannot be employed in a medium which is neutral or possesses a low acidity. 

During the course of a polyesterification the volume and the weight of the reaction mixture vary because condensation water is released. In most cases, the progress of the reaction is followed by titration of the acid groups at definite intervals the carboxy group concentration is expressed in equivalents per kilogram. Consequently, several authors tried to find out if the weight decrease due to the elimination of water must be taken into account. 

Lippi et. al (87) and Dirstine (88) circumvented titration by converting the liberated fatty acids into copper salts, which after extraction in chloroform are reacted with diethyldithio-carbamate to form a colored complex which is measured photometrically. While the end point appears to be more sensitive than the pH end point determination, the advantages are outweighed by the additional steps of solvent extraction, centrifugation and incomplete extraction when low concentrations of copper salts are present. Other substrates used for the measurement of lipase activity have been tributyrin ( ), phenyl laurate (90), p-nit ro-pheny1-stearate and 3-naphthyl laurate (91). It has been shown that these substrates are hydrolyzed by esterases and thus lack specificity for lipase. Studies on patients with pancreatitis indicate olive oil emulsion is definitely superior to water soluble esters as substrates for measuring serum lipase activity. 

Definitions. Titrimetric Reactions. Acid-base Titrations. Applications of Acid-base Titrations. Redox Titrations. Applications of Redox Titrations. Complexometric Titrations. Ethylenediaminetetraacetic Acid (EDTA). Applications of EDTA Titrations. Titrations with Complexing Agents Other Than EDTA. Precipitation Titrations. ... 

The problem the analyst has is to choose indicators that change color close enough to an equivalence point so that the accuracy of the experiment is not diminished, which really means at any point during the inflection point. (Refer to Section 4.2 for the definitions of equivalence point and end point.) It almost seems like an impossible task, since there must be an indicator for each possible acid or base to be titrated. Fortunately, there are a large number of indicators available, and there is at least one available for all acids and bases, with the exception of only the extremely weak acids and bases. Figure 5.5 lists some of these indicators and shows the pH ranges over which they change color. 

Volumetric Estimation.—Tellurium may be determined by oxidation from the tellurous to the telluric condition, using an excess of potassium dichromatc or permanganate and subsequently titrating the excess of oxidising agent with a standard solution of a suitable reducing agent.2 In order to obtain accurate results with the potassium dichromate titration, certain very definite steps in the procedure are essential, and it is necessary to control the course of the reaction, since hydrochloric and telluric acids interact with production of chlorine. 

In a definitive series of experimental investigations H. N. Wilson showed that the quinolinium salt, (C isNJ fPCV I2M0O3]3- was anhydrous, contained exactly 12 moles of molybdenum trioxide per mole of phosphate, that the precipitate had a negligible solubility and could be dried to constant weight in two hours at 105 °C. This precipitate also lent itself to a precise alkalimetric titration. In the presence of citric acid interference by silica was inhibited so that the method was admirably suitable for the analysis of basic slags or fertilizers.34... 

In presence of appreciable amounts of volatile adds, a separate weighed portion of the substance is mixed with cold water to a definite volume and an ab quot part of the liquid decanted or, if necessary, filtered through glass wool, and titrated as above (total acidity). The fixed acidity is determined by evaporating almost to dryness on a water-bath a known volume of the solution obtained as in 2 (above), the residue being taken up in water and titrated as before volatile acidity = total acidity minus fixed aridity. 

The above methods cannot be used if the spirit contains chlorides, as may happen if it has been broken down with water containing these salts. In this case the total hydrocyanic acid may be determined by distilling 100 c.c. of the spirit and collecting at least three-quarters (which will contain all the hydrocyanic acid present) in a dilute solution of silver nitrate of known titre. The liquid is then made up to a definite volume and filtered, the excess of silver in an aliquot part of the filtrate being titrated with thiocyanate as already described. The free hydrocyanic acid, in presence of chlorides, should be determined colorimetrically as follows a solution of about 0-05 gram of potassium cyanide per litre is prepared and its exact content of HCN determined by titration with silver nitrate and ammonium thiocyanate. In a series of test-tubes are placed such quantities of this... 

Ferric Oxide.—The filtrate from the preceding determination is made up, together with the wash water, to a definite volume (e.g., 250 c.c.) and an aliquot part of it (50 or 100 c.c.) precipitated with ammonia in presence of ammonium chloride the predpitate is collected on a filter and washed. If alumina is present only in negligible quantity, the weight of the caldned predpitate gives the ferric oxide. In the contrary case, the washed and still wet predpitate is dissolved in dilute sulphuric acid and the solution made up to 100 c.c. with water 10 c.c. of this solution are reduced with zinc and the ferrous iron titrated with permanganate (see Vol. I, Limestones and Marls, p. 142). 

The solubility is thus very great, and in the interval between 0° and 40°, there is no sign of the formation of a definite hydrate. H. Rose observed no development of hydrogen when the phosphites are boiled with alkali hydroxides. A. Italiener studied the titration of phosphorous acid with alkali-lye. 

Bernasconi, Koch, and Zollinger measured the IEs on acidity due to ring deuteration in some anilinium ions.49 The results are listed in Table 4. Deuterium definitely decreases acidity, but it was not possible to distinguish whether the IE decreases with increasing distance of the isotope or whether meta deuterium is ineffective compared to ortho (and perhaps para). A tentative answer to this question comes from phenols (Table 3),32 where the IEs are large enough and the NMR titration method accurate enough to show that there is no decrease as the site of deuteration moves from ortho to meta to para. 

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