Solution pH Determination

The use of fluorescent dyes as pH indicators has been well documented in the literature. 14, a 2,1 94) Numerous indicators with spectral characteristics in the visible 

Variations in absorption and fluorescence spectra of indicator dyes are usually associated with an alteration in the degree of conjugation on ionization of the 

The protonation of the dye assuming a 1 1 ratio and that no other ions form part in the equation can be represented as 

The optical fiber s response can be determined following the same steps as in the case for the metal ions. Hence we get 

A plot of l//f versus pH produces a straight line and the equilibrium constant, Afop, can be calculated from the slope. 

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Selectivity for carbonate in a competitive anion background (30 mM carbonate, 100 mM NaCl, 0.9 mM phosphate, 2.3 mM lactate, 0.13 mM citrate) simulating an extracellular anionic environment has been assessed [7], The solution pH determines... 

In this experiment the concentrations of Ga + and Mg + in aqueous solutions are determined by titrating with EDTA. The titration is followed spectrophotometrically by measuring the absorbance of a visual indicator. The effect of changing the indicator, the pH at which the titration is carried out, and the relative concentrations of Ga + and Mg + are also investigated. 

Colorimetric Method. A finely powdered sample treated with sulfuric acid, hydrobromic acid [10035-10-6] and bromine [7726-95-6] gives a solution that when adjusted to pH 4 may be treated with dithi one [60-10-6] ia / -hexane [110-54-3] to form mercuric dithi2onate [14783-59-6] (20). The resultant amber-colored solution has a color iatensity that can be compared against that of standard solutions to determine the mercury concentration of the sample. Concentrations below 0.02 ppm have been measured by this method. 

Solubihty data ia water are given ia Figure 5 and ia Table 9, solution pH ia Table 10, and the solubiUty ia organic solvents is given ia Table 7. Heats of solution ia water have been determined (68,73). The pentahydrate, ia contact with its aqueous solution, is metastable with respect to the tetrahydrate (kernite) at temperatures above 58.2°C and metastable to borax decahydrate below 60.6—60.8°C. Kernite can be slowly crystallised from a near saturate... 

Procedure To an aliquot of the sample solution containing 12.5 - 305 p.g of platinum(IV) were added 5 ml of hydrochloric acid - sodium acetate buffer of pH 2.1, 1 ml of O.IM Cu(II) sulphate solution, and 3.0 ml of 0.5% propericiazine solution. The solution was diluted to 25 ml with distilled water, mixed thoroughly, and the absorbance measured at 520 nm against a reagent blank solution after 10 min. The platinum concentration of the sample solution was determined using a standar d calibration curve. 

The glass pH electrode has been the most widely used tool for measurement of pH. Optical pH sensing is one of the most well established methods of pH determinations, which is based on measurements of the absorption spectmm of an indicator, either dissolved in the test solution or immobilized on a substrate. 

Certain alloys frequently used in cooling water environments, notably aluminum and zinc, can be attacked vigorously at high pH. These metals are also significantly corroded at low pH and thus are said to be amphoteric. A plot of the corrosion behavior of aluminum as a function of pH when exposed to various compounds is shown in Fig. 8.1. The influence of various ions is often more important than solution pH in determining corrosion on aluminum. 

As with simple imines, the identity of the rate-limiting step changes with solution pH.. s the pH decreases, the rate of the addition decreases because protonation of the amino compound reduces the concentration of the nucleophilic unprotonated form. Thus, whereas the dehydration step is normalfy rate-determining in neutral and basic solution, addition becomes rate-determining in acidic solutions. 

Titration is the analytical method used to determine the amount of acid in a solution. A measured volume of the acid solution is titrated by slowly adding a solution of base, typically NaOH, of known concentration. As incremental amounts of NaOH are added, the pH of the solution is determined and a plot of the pH of the solution versus the amount of OH added yields a titration curve. The titration curve for acetic acid is shown in Figure 2.12. In considering the progress of this titration, keep in mind two important equilibria ... 

The pH of the reaction mixture is taken both before and after the addition of the last portion of the quinidine-methanol solution. The mixture is gently warmed (30° to 50°C), and the pH determined at 20 minute intervals. At the end of 4 hours, or when the reaction has gone to completion as evidenced by the pH of the mixture (between pH 6.5 and 7.5), the stirring is then stopped and the mixture cooled to 0°C and filtered. The solvent is evaporated to dryness under reduced pressure, utilizing as little heat as is feasible. The dried residue Is powdered and suspended in 10 volumes of methanol and filtered. The insoluble powder is dried, and is quinidine polygalacturonate, melting at 180°C with decomposition. 

The Nernst equation shows that the glass electrode potential for a given pH value will be dependent upon the temperature of the solution. A pH meter, therefore, includes a biasing control so that the scale of the meter can be adjusted to correspond to the temperature of the solution under test. This may take the form of a manual control, calibrated in 0 C, and which is set to the temperature of the solution as determined with an ordinary mercury thermometer. In some instruments, arrangements are made for automatic temperature compensation by inserting a temperature probe (a resistance thermometer) into the solution, and the output from this is fed into the pH meter circuit. 

The complexation of Pu(IV) with carbonate ions is investigated by solubility measurements of 238Pu02 in neutral to alkaline solutions containing sodium carbonate and bicarbonate. The total concentration of carbonate ions and pH are varied at the constant ionic strength (I = 1.0), in which the initial pH values are adjusted by altering the ratio of carbonate to bicarbonate ions. The oxidation state of dissolved species in equilibrium solutions are determined by absorption spectrophotometry and differential pulse polarography. The most stable oxidation state of Pu in carbonate solutions is found to be Pu(IV), which is present as hydroxocarbonate or carbonate species. The formation constants of these complexes are calculated on the basis of solubility data which are determined to be a function of two variable parameters the carbonate concentration and pH. The hydrolysis reactions of Pu(IV) in the present experimental system assessed by using the literature data are taken into account for calculation of the carbonate complexation. 

The electrical double layer at pc-Zn/fyO interfaces has been studied in many works,154 190 613-629 but the situation is somewhat ambiguous and complex. The polycrystalline Zn electrode was found to be ideally polarizable for sufficiently wide negative polarizations.622"627 With pc-Zn/H20, the value of Eg was found at -1.15 V (SCE)615 628 (Table 14). The values of nun are in reasonable agreement with the data of Caswell et al.623,624 Practically the same value of Eff was obtained by the scrape method in NaC104 + HjO solution (pH = 7.0).190 Later it was shown154,259,625,628 that the determination of Eo=0 by direct observation of Emin on C,E curves in dilute surface-inactive electrolyte solutions is not possible in the case of Zn because Zn belongs to the group of metals for which E -o is close to the reversible standard potential in aqueous solution. 

The potentiometric titration was carried out in order to determine the functional groups present in the biomass surface. During the titration experiments, the C02-free condition was always maintained to avoid the influence of inorganic carbon on the solution pH. Detailed potentiometric titration procedure and estimation method of functional groups are available in the previous reports [4,6]. 

Figure 17-3 shows the range of pH and hydronium ion concentrations. The measurement of pH is a routine operation in most laboratories. Litmus paper, which turns red when dipped in acidic solution and blue when dipped in basic solution, gives a quick, qualitative indication of acidity. As Figure 17-4 shows, approximate measures of pH can be done using pH paper. Universal pH paper displays a range of colors in response to different pH values and is accurate to about 0.5 pH unit. For quantitative pH determinations, scientists use pH meters. 

As an example, consider the titration of 0.150 L of 0.500 M acetic acid solution with 2.50 M potassium hydroxide. Very early in the titration, the major species are water and acetic acid, and the equilibrium that determines solution pH is proton transfer between these major species ... 

Four anthocyanin species exist in equilibrium under acidic conditions at 25°C/ according to the scheme in Figure 4.3.3. The equilibrium constant values determine the major species and therefore the color of the solution. If the deprotonation equilibrium constant, K, is higher than the hydration constant, Kj, the equilibrium is displaced toward the colored quinonoidal base (A), and if Kj, > the equilibrium shifts toward the hemiacetalic or pseudobase form (B) that is in equilibrium with the chalcone species (C), both colorless." - Therefore, the structure of an anthocyanin is strongly dependent on the solution pH, and as a consequence so is its color stability, which is highly related to the deprotonation and hydration equilibrium reaction constant values (K and Kj,). 

V0x/Zr02 catalysts were designated as ZVx(y)pHz, where x gives the analytical vanadium content (weight percent), y specifies the preparation method (a, adsorption, i, impregnation or acac, acetylacetonate) and z the AV solution pH. The V-content was determined by atomic absorption (Varian Spectra AA-30) after the sample had been dissolved in a concentrated (40%) HF solution. 

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