Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Neutralization titrations buffer solution

Now consider the overall shape of the pH curve. The slow change in pH about halfway to the stoichiometric point indicates that the solution acts as a buffer in that region (see Fig. 11.3). At the halfwayr point of the titration, [HA] = [A ] and pH = pfCa. In fact, one way to prepare a buffer is to neutralize half the amount of weak acid present with strong base. The flatness of the curve near pH = pKa illustrates very clearly the ability of a buffer solution to stabilize the pH of the solution. Moreover, we can now see how to determine pKa plot the pH curve during a titration, identify the pH halfway to the stoichiometric point, and set pKa equal to that pH (Fig. 11.8). To obtain the pfCh of a weak base, we find pK3 in the same way but go on to use pKa -1- pfq, = pKw. The values recorded in Tables 10.1 and 10.2 were obtained in this way. [Pg.578]

In the process of a weak acid or weak base neutralization titration, a mixture of a conjugate acid-base pair exists in the reaction flask in the time period of the experiment leading up to the inflection point. For example, during the titration of acetic acid with sodium hydroxide, a mixture of acetic acid and acetate ion exists in the reaction flask prior to the inflection point. In that portion of the titration curve, the pH of the solution does not change appreciably, even upon the addition of more sodium hydroxide. Thus this solution is a buffer solution, as we defined it at the beginning of this section. [Pg.113]

An acid-base titration is a method that allows quantitative analysis of the concentration of an unknown acid or base solution. In an acid-base titration, the base will react with the weak acid and form a solution that contains the weak acid and its conjugate base until the acid is completely neutralized. The following equation is used frequently when trying to find the pH of buffer solutions. [Pg.14]

The base should be a strong buffer. A comparison of the titration of 0.2 N KOH and 0.2 N K2C03 adjusted to pH 12 shows that it is easier to exceed the acid-neutralizing capacity of the KOH compared with the buffered solution of K2C03 (see Figure 4). [Pg.334]

PThe values of pK for a particular molecule are determined by titration. A typical pH dependence curve for the titration of a weak acid by a strong base is shown in figure 3.2. The concentration of the anion equals the concentration of the acid when the acid is exactly half neutralized. Note that at this point on the curve, the pH is least sensitive to the quantity of added base (or acid). Under these conditions, the solution is said to be buffered. Biochemical reactions are typically highly dependent on the pH of the solution. Therefore, it is frequently advantageous to study reactions in buffered solutions. The ideal buffer is one that has a pK numerically equivalent to the working pH. [Pg.53]

The neutralization reaction goes to completion, but the amount of H30 + added before the equivalence point is not sufficient to convert all the NH3 to NH4+. We therefore have an NH4+-NH3 buffer solution, which accounts for the leveling of the titration curve in the buffer region between the start of the... [Pg.684]

Unfortunately, the dependence of the rates on pH cannot be measured by our method since acidimetric titrations are not possible in buffered solutions. However, in weakly acidic and neutral solutions, there cannot be much influence because otherwise no rate constants could have been obtained. In alkaline solution, on the other hand, a base induced fragmentation occurs, which is faster by some powers of 10 than the solvent fragmentation. Thus, in 0.025N methanolic NaOH at 0°C, the half lifetime of stilbene ozonide is only 2 minutes. [Pg.33]

Isophane insulin is produced by titration of an acidic solution of insulin with a buffered solution of protamine at neutral pH until so-called isophane precipitation occurs that is, no insulin or protamine is present in the supernatant. Under these conditions the precipitate consists of rod-shaped crystals. [Pg.353]

Substantial efforts have been devoted to the development of molecular sensors for dopamine. Raymo et al.70 reported a two-step procedure to coat silica particles with fluorescent 2,7-diazapyrenium dications sensing toward dopamine. The analysis of the fluorescence decay with multiple-equilibria binding model revealed that the electron deficient dications and the electron-rich analytes form 1 1 and 1 2 complexes at the particle/water interface. The interfacial dissociation constants of the 1 1 complexes were 5.6mM and 3.6mM for dopamine and catechol, respectively. Dopamine was dominated by the interaction of its electron-rich dioxyarene fragment with the electron-deficient fluorophore in neutral aqueous environments. Ahn et al.71 reported tripodal oxazoline-based artificial receptors, capable of providing a preorganized hydrophobic environment by rational design, which mimics a hydrophobic pocket predicted for a human D2 receptor. A moderate binding affinity, a dissociation constant of 8.2 mM was obtained by NMR titrations of tripodal oxazoline-based artificial receptor with dopamine in a phosphate buffer solution (pH 7.0). Structurally related ammonium ions, norepinephrine, 2-phenylethylamine,... [Pg.264]

Preparation of suitable indicator solutions. The prepar on of indicator solutions for use in the colorimetric pH determination has already been described in detail in Chapter Five ( 3). These solutions, however, were suited only for measurements of buffered solutions. Isohydric indicator solutions have to e prepared in another manner. H. T. Stern titrates the indicator with sodium hydroxide and measures the pH during neutralization with the quinhydrone electrode. A similar procedure has been described by Pierre and Fxjdge. Fawcett and Acree keep in stock a large series of neutralized indicator solutions and determine their pH approximately by colorimetric means. [Pg.328]

It frequently happens that hydrogen ions are removed from solution by impurities in the indicator or in the paper, or as a result of adsorption by the paper. In other words, the solution apparently is neutralized. The use of a buffer mixture, however, counteracts the influence of traces of impurities. The sensitivity of indicator papers is found to be the same as that of the corresponding indicator solutions when measured in the presence of buffer solutions. For strong electrolytes, the indicator papers measure the titration acidity rather than the hydrogen ion concentration. [Pg.367]

These stages are characterized by the equilibrium constant values (pK) equal to -6.5 0.2 and -5.23 0.3, respectively. The buffer solutions, whose formation corresponds to the section of the titration curves with h 1 and the neutralization stage (1.2.86), are characterized by the buffer number of -0.03, whereas for the section conforming to the equation (1.2.87) this value is markedly higher (up to — 0.05). [Pg.86]

If the soil is leached with buffer solution until the soil pH equals that of the buffer, titrating the remaining buffer capacity of the solution measures the soil acidity that must be neutralized to produce a soil pH equal to that of the buffer. A more rapid method is add buffer solution to soil without attempting to bring the final pH of the... [Pg.270]

The buffer value of a solution can be evaluated from the course of the neutralization titration curve. It is a reciprocal value of the tangent to the titration curve expressing the dependence pH = for the given points. The buffer value is given in mmol 1 and is always positive. [Pg.106]

This is a half-neutralized phosphoric acid solution its principal ionic constituents and their concentrations are Na+, 0.3 M HPO4, 0.1 M H2P04, 0.1 M H", about 10 M. From the titration curve of Figure 12-4 we see that this solution is a good buffer to change its pH from 7 to 6.5 or 7.5 (tripling the hydrogen ion or hydroxide ion concentration) about... [Pg.400]

To 100 ml of a neutral solution containing about 20 mg of manganese add a small amount of hydroxylamine hydrochloride to prevent oxidation of the manganese. Then add 10 ml of ammonia buffer solution followed by 3 to 5 drops of catechol violet indicator and titrate immediately with 0 01 M EDTA until the colour changes from greenish-blue to reddish-purple. 1 ml O OIM EDTA = 0 0005493 g manganese. [Pg.425]

Buffer Solutions 17-3 Acid-Base Indicators 17-4 Neutralization Reactions and Titration Curves... [Pg.789]

The slope of the tangent to the curve at the inflection point where oc = is thus inversely proportional to the number of electrons n. The E-oc curves are similar to the titration curves of weak acids or bases (pH-or). For neutralization curves, the slope dpH/doc characterizes the buffering capacity of the solution for redox potential curves, the differential dE/da characterizes the redox capacity of the system. If oc — for a buffer, then changes in pH produced by changes in a are the smallest possible. If a = in a redox system, then the potential changes produced by changes in oc are also minimal (the system is well poised ). [Pg.190]

Procedure Weigh accurately about 0.8 g of granulated zinc, dissolve by gentle warming in 12 ml of dilute hydrochloric acid and 5 drops of bromine water. Boil to remove excess bromine, cool and add sufficient DW to produce 200 ml in a volumetric flask. Pipette 20 ml of the resulting solution into a flask and neutralize carefully with 2 N sodium hydroxide. Dilute to about 150 ml with DW, add to it sufficient ammonia buffer (pH 10.0) to dissolve the precipitate and add a further 5 ml quantity in excess. Finally add 50 mg of Mordant Black II mixture and titrate with the disodium edetate solution until the solution turns green. Each 0.003269 g of granulated zinc is equivalent to 1 ml of 0.05 M disodium ethylenediaminetetracetate. [Pg.166]


See other pages where Neutralization titrations buffer solution is mentioned: [Pg.1163]    [Pg.827]    [Pg.1432]    [Pg.113]    [Pg.113]    [Pg.178]    [Pg.349]    [Pg.61]    [Pg.90]    [Pg.215]    [Pg.23]    [Pg.199]    [Pg.1514]    [Pg.187]    [Pg.33]    [Pg.29]    [Pg.267]    [Pg.295]    [Pg.1141]    [Pg.267]    [Pg.690]    [Pg.392]    [Pg.163]    [Pg.1420]    [Pg.260]    [Pg.344]    [Pg.220]    [Pg.279]    [Pg.137]   
See also in sourсe #XX -- [ Pg.3755 ]




SEARCH



Buffer neutralization titration

Buffer solution Titration

Buffer solutions

Buffered solution

Neutral buffers

Neutral solutes

Neutral, solutions neutralization

Neutralization titrations

© 2024 chempedia.info