Potentiometric studies on the composition of cobalt ferrocyanide complex

Summary The formation and precipitation of cobaltferrocyanide has been studied by potentiometric titrations between cobalt nitrate and potassium ferrocyanide using ferricyanide-ferrocyanide electrode both by the direct and the inverse methods. The end point obtained from the maximum value of E/C corresponds to the formation of a compound having the composition 4Co₂Fe(CN)₂ · 3K₄Fe(CN)₆ with either of the substance used as the reagent. The titration curves have a regular shape, a sharp break in potential occurs at the end point and the results are accurate and reproducible. The effects of electrolytes and alcohol in varying concentrations on the end point as well as on the nature of the curves has been studied. In presence of 30% alcohol, the observed titre values closely approach the calculated points of equivalence required for the formation of the above compound.     

Potentiometric determination of cephalothin

The composition of a pseudo-liquid potential-determining phase for the cephalothin-selective electrode has been determined and the following basic electrode parameters were examined: measurement range, slope, limit of detection, selectivity and lifetime. This paper discusses the effect of side-chain substituents on the electrode properties, the electrode having been used for cephalothin determination in the range 43-436.5 mg l-1 (standard deviation, 0.64-4.5 mg l-1).     

Extractive separation and spectrophotometric determination of tungsten as ferrocyanide

Tungsten, in amounts ranging from micrograms to milligrams, can be extracted into isoamyl alcohol, as the tungsten(V) ferrocyanide complex obtained by reduction of tungsten(VI) with tin(II) in 4M hydrochloric acid containing ferrocyanide. It can thus be separated from iron, cobalt, chromium, manganese, arsenic, antimony, bismuth, silicon, calcium and copper, their precipitation being prevented by addition of glycerol and, in the case of iron, sulphosalicyclic acid. Molybdenum, vanadium and nickel are not separated from tungsten, however. Tungsten can also be determined spectrophotometrically as tungsten(V) ferrocyanide. The absorbance of the brown complex is measured in aqueous solution or preferably after extraction into isoamyl alcohol. As many alloying elements interfere, they should be separated by the ferrocyanide extraction or other suitable method. Both the separation and the determination methods give satisfactory results with an overall error of not more than 0.5% in the analysis of practical samples containing low or high percentages of tungsten.     

Potentiometric and thermometric determination of mercaptopyrimidines

Summary Potentiometric and Thermometric Determination of Mercaptopyrimidines Potentiometric and thermometric methods for the determination of several 2- and 6-mercaptopyrimidines are described. Mercapto groups can be titrated as acids in water or in dimethylformamide media. The use of acetic acid as solvent allows titration of the basic pyrimidine nucleus. Thermometric titrimetry is also a valuable procedure for the titration of mercapto groups, either directly with sodium hydroxide or by back-titration with hydrochloric acid after addition of excess of alkali. About 10–25 mg of sample can be determined with an error better than 1%.     

Potentiometric studies on sodium dehydrocholate micelles

The scarcely studied sodium dehydrocholate-water system was investigated at low concentration by using H⁺-, Na⁺- and dehydrocholate-ion-selective electrodes. The findings at concentrations below the critical micelle concentration are consistent with those of previous work. A dimeric chelate structure entrapping Na⁺ ions at very low concentration is proposed. The composition of the micelles and the degree of ionisation were studied and explained as the result of the possibility of a back-to-face mechanism of aggregation of this steroid salt. This mechanism also explains the possibility of formation of acid soaplike aggregates at intermediate concentrations.     

Potentiometric determination of 8-chlorotheophylline

Two methods are described for the potentiometric determination of 8-chlorotheophylline in aqueous solution. Both methods are based on the reaction of 8-chlorotheophylline with silver ions. In the first, the nitric acid produced in the reaction is titrated with sodium hydroxide. In the second, the 8-chlorotheophylline is titrated directly with silver nitrate in sodium carbonate medium. Both methods give reasonably accurate and reproducible results, and are suitable for the assay of 8-chlorotheophylline in pharmaceutical preparations.     

Potentiometric determination of potassium ferricyanide

A rapid and accurate electrometric method for the determination of potassium ferricyanide solutions has been investigated. It consists in titrating ferricyanide solutions potentiometrically against standard AgNO₃, using a silver indicator electrode in conjunction with a saturated calomel electrode connected by a KNO₃ bridge. Either of the reagents may be used as the titrant. A marked change in e.m.f is observed at thc end-point corresponding to the formation and precipitation of Ag³[Fe(CN)₆]. The curves have a regular form, a pronounced maximum in dE/dV occurs at the end-point and the results are very accurate and reproducible. The reaction, though simple, affords a quantitative method for the determination of ferricyanide or silver. The effect of neutral salts and ethanol on the accuracy of the end-point has been studied.     

The catalytic determination of mercury with potassium ferrocyanide and nitrosobenzene

Mercury can be determined in quantities of about 1 μg by catalytic effects on the decomposition of K₄[Fe(CN)₆]. The reaction product formed in a given period is measured colorimetrically at 5280 À after addition of nitrosobenzene. There appears to be a linear relation between the extinction and the logarithm of the mercury concentration. As compared with the original method by Asperger and Murati the standard deviation can be reduced from 9.5 to 5.0 % by buffering the reaction mixture at an optimum pH, i.e. 3.9–4.1.     

Potassium ferrocyanide as a spectrophotometric reagent for the determination of uranium

Potassium ferrocyanide gives a colour reaction with U(VI), which is suitable for its determination. The complex absorbs in the wavelength range of 390–397 nm. The optimum pH range for colour development was 1.5–3.5. The molar absorptivity was found to be 4.65·10³ 1·mol^–1·cm^–1. Most of the anions up to 1000 g did not interfere. The method was made selective by extracting U(VI) first with DOSO from the mixture of interfering cations from 1–2M HNO₃ medium and then determining uranium in the back-extracted solution by developing the colour with ferrocyanide. 20 g/10 ml of U(VI) in the final solution could be satisfactorily determined within an RSD of ±2%.     

Potentiometric flow-injection determination of iodide and iodine

A potentiometric flow-injection system is described, in which iodide in the concentration range 10(-6)-10(-1)M may be determined at rates of up to 360 samples/hr at a flow-rate of 17.8 ml/min. Iodine, after on-line reduction to iodide with 0.1M sodium metabisulphite, can also be determined, with a throughput of 60 samples/hr for 10(-5)-10(-3)M iodine. Analyses of two pharmaceutical preparations for iodide and iodine are reported, and the results are in reasonable agreement with titrimetric values.     

Potentiometric and volumetric determination of 6-mercaptopurine

Three methods for the determination of 6-mercaptopurine in the pure state and in tablets are described. One method is based on the reaction of this compound with silver ions, whereby an equivalent amount of nitric acid is liberated, the latter being determined potentiometrically with sodium hydroxide. The other two methods involve titration with chloramine-T, with potentiometric and visual end-point-detection. All methods afford accurate and reproducible results and can be used for routine assay of 6-mercaptopurine in tablets.     

Potentiometric stripping analysis for bismuth(III) in seawater

Total bismuth(III) in seawater can be determined either directly after acidification with 0.1 M hydrochloric acid or after co-precipitation with magnesium hydroxide by means of pre-electrolysis for 8 min at —0.90 V vs. SCE at a rotated glassy carbon/mercury film electrode prior to potentiometric stripping analysis. The limits of detection (2σ) are 0.6 and 0.003 nM, respectively. Three Kattegatt surface seawater samples were found to contain bismuth(III) concentrations of 5–12 pM (l–2.5 ng l^-1).     

Potentiometric determination of aminal stability constants

Potentiometric titration was used to determine the logarithms of the stepwise equilibrium constants for the species formed between morpholine and formaldehyde in aqueous solution, ionic strength 0.5 and 2.5M (KCl) at 25 degrees C. The instrumental and computational techniques developed for metal-ligand stability constant determination were applied. Formaldehyde is equivalent to the metal-ion and is represented by M while neutral morpholine is equivalent to the ligand and is represented by L. The stability constants of the following equilibria were determined by non-linear regression (figures in parentheses are at ionic strength 2.5 M KCl): M + L left arrow over right arrow ML (hemi-aminal) logK(1) = 2.90 +/- 0.02 (2.980 +/- 0.004); ML + L left arrow over right arrow ML(2) (bis-aminal); log K(2) = 1.3 +/- 0.2 (1.41 +/- 0.07); MLH left arrow over right arrow ML + H(+) (protonated hemi-aminal) pK(a) = 5.87 +/- 0.01 (6.411 +/- 0.005); ML(2)H left arrow over right arrow ML(2) + H(+) (protonated bis-aminal) pK(a) = (7.6 +/- 0.2). the pK(a) of the protonated bis-aminal could only be determined at the higher ionic strength. The results are in good agreement with reported values determined using the classic formol titration. The automated titration system acquired the full time course of the pH change upon each titrant addition allowing a kinetic analysis to be performed as well as an equilibrium analysis. The forward and reverse rate constants for M + L left arrow over right arrow ML were 0.77M(-1) sec(-1) and 8.1 x 10(-4) sec(-1). respectively.     

Potentiometric sensors for the determination of water-soluble polyelectrolytes

Potentiometric sensors for the analysis of water-soluble polyelectrolytes with different molecular masses were proposed. The surface morphology of polyvinyl chloride sensor membranes and chemical analytical characteristics of ready devices were studied. Selectivity coefficients of the sensors were calculated.     

Potentiometric determination of silver with dithiooxamide

Potentiometric titration with dithiooxamide solution can be used to determine silver in the 0.0100–50.0 p.p.m range with an average accuracy of ca. 0.5% and a relative standard deviation ranging from 1.26% to 0.03% The metals commonly associated with silver can be masked with fluoride and EDTA The advantages of the method over other potentiometric and common spectrophotometric methods are outlined.     

Potentiometric determination of dialysate urea nitrogen

An enzymatically modified ammonium ion-selective electrode has been applied for the determination of urea in spent dialysate. The biosensor has been used in a simple flow-injection analysis (FIA) system. The system enables one to perform over 25 dialysate urea nitrogen (DUN) determinations per hour. The interferences from other components of posthemodialysis fluid were eliminated by simultaneous measurements with non-modified enzymatically ion-selective electrode. It is possible to use both the sensors in a simplified differential potentiometric system. The results of DUN determination using the biosensor/FIA system and a conventional method of urea determination were comparable. The presented analytical system can potentially find wider biomedical application in the monitoring of hemodialysis progress.     

Potentiometric and spectrophotometric determination of the protonation constant of hexamethylenetetramine

The protonation constant of hexamethylenetetramine (urotropine) was determined by a potentiometric and a spectrophotometric method. The calculations gave log K_HL (concentration constants): 4·89 at μ = 0·1 and 5·05 at μ = 0·5. The temperature was 25° and potassium chloride was used to adjust the ionic strength.     

Potentiometric and spectrophotometric determination of the dissociation constants of cefetamet

Summary The dissociation constants of cefetamet-Na have been determined using potentiometric titrations and spectrophotometry. The investigations were carried on in water solutions at constant temperature and ionic strength, and at differentH ₀ andpH values. Potentiometric investigations were performed at three different temperatures and ionic strengths. The concentration dissociation constants and the corresponding thermodynamic dissociation constants were calculated by a computer program. The mixed dissociation constants (pK) of cefetamet-Na have been determined spectrophotometrically in theH ₀ range from -5.80 to 0.00 and atpH values from 0.00 to 12.70 and are in good agreement with values achieved by graphical methods as well as with those obtained by potentiometric methods. Based on the determined values, the thermodynamic parameters (G, H, S) were calculated atI=0.1M.

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Potentiometrische und spektrophotometrische Bestimmung der Dissoziationskonstanten von Cefetamet

Zusammenfassung Die Dissoziationskonstanten von Cefetamet-Na wurden mittels potentiometrischer Titrationen und auf spektrophotometrischem Weg bestimmt. Die Untersuchungen wurden in wäßriger Lösung bei konstanter Temperatur und Ionenstärke und verschiedenenH ₀- undpH-Werten durchgeführt. Potentiometrische Messungen wurden bei drei verschiedenen Temperaturen und Ionenstärken vorgenommen. Die stöchiometrische Dissozation und die entsprechenden thermodynamischen Dissoziationskonstanten wurden mit Hilfe eines Computerprogramms berechnet. Die gemischten Dissoziationskonstanten (pK) wurden spektrophotometrisch imH ₀-Bereich von -5.80 bis 0.00 und impH-Bereich von 0.00 bis 12.70 bestimmt und stimmen sowohl mit Werten, die mit Hilfe der graphischen Methode erhalten wurden, als auch mit potentiometrisch bestimmten gut überein. Aus den ermittelten Werten der Dissoziationskonstanten wurden die thermodynamischen Parameter (G, H, S) fürI=0.1M berechnet.