Spectrophotometric applications

Beer s law states that absorbance is an additive property of all the absorbing molecules present in a mixture (see Eqn. 7.10). In principle, n absorbance measurements at n different wavelengths are needed to determine the concentrations of n components in a mixture this procedure gives n independent simultaneous equations in n unknowns. The molar absorptivities must be known or determined for each individual absorbing species, 1, 2, etc., at each wavelength. If, in a two-component mixture, the values are ci, 2 at wavelength A, and e[, at a second wavelength, A, and the 

The spectrophotometric method is particularly valuable for studying complexes of low stability. Consider the formation of a complex M Lp, where M is a metal ion and L is a ligand  

The molar ratio of the two components of a complex is important. In a quantitative determination, an excess of ligand should be added in order to force the equilibrium toward completion. 

Molar-Ratio Method. In this method, the concentration of one component is kept fixed and that of the other varied to give a series of [L]/[M] ratios. The absorbances of these solutions, measured at an absorption maximum for the complex M Lp, increase linearly up to the molar ratio of the complex, at which virtually the whole amount of both components is complexed (assuming little dissociation). Further addition of component L cannot increase the absorbance, and the line becomes horizontal, or shows a break if component L absorbs at the same wavelength (Fig. 

In rare cases, an excess component L may cause a decrease in absorbance owing to the stepwise formation of higher-order complexes that have smaller e values at this wavelength. The composition of molybdogermanic acid has been studied by the molar-ratio method [13] showing a ratio of 36 molybdate 1 germanate. 

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Pyrolysis can also be used in flow-based determinations with electrothermal atomic absorption spectrometry, as demonstrated in the determination of nickel in environmental and biological reference materials using a sequential injection system with renewable beads [313]. After analyte sorption, the beads were directed towards the furnace of the spectrometer and stopped there pyrolysis was accomplished as usual in order to release the analyte and destroy the beads. This innovation has often been exploited in the lab-on-valve system, but spectrophotometric applications have not been proposed to date. 

Owing to technical obstacles discussed in the previous paragraphs, the enhancement in sensitivity and selectivity in spectrophotometric applications using on-line columns are not as dramatic as for atomic spectrometric methods. EF values of 10-15, with sampling frequencies of 20 - 30 h are typical for preconcentrations, yielding CE values of... 

Although applications for column separation or preconcentration systems coupled to chemiluminescence determinations are few, published reports show no particular difficulties in such applications, except for the requirement of an adjustment of the chemical conditions of the eluate to suit the chemiluminescence reaction. Interferences due to refractive index effects are not likely to occur, owing to the often used spiral shape of the chemiluminescence flow-cell and to the fact that light emission is measured perpendicular to the direction of the flow. Therefore, column washing is usually not as important as for spectrophotometric applications, so that time-based sample loading manifolds such as those used for flame AAS may be used to advantage for improving the concentration, efficiencies. 

Zrimsek, R Kune, J. Kosec, M. Mrkun, J. Spectrophotometric application of resazurin reduction assay to evaluate boar semen quality. Int. J. Androl. 2004,27, 57-62. 

Davies and Warren have investigated the nitration of naphthalene, ace-naphthene and eight dimethylnaphthalenes in acetic anhydride at o °C. Rates relative to naphthalene were determined by the competition method, and the nitro-isomers formed were separated by chromatographic and identified by spectrophotometric means. The results, which are summarised in the table, were discussed in terms of various steric effects, and the applicability of the additivity rule was examined. For the latter purpose use was made of the data of Alcorn and Wells (table 10.2) relating to the nitration of monomethyl-naphthalenes at 25 °C. The additivity rule was found to have only limited utility, and it was suggested that the discrepancies might be due in part to the... 

The majority of FI A applications are modifications of conventional titrimetric, spectrophotometric, and electrochemical methods of analysis. For this reason it is appropriate to evaluate FIA in relation to these conventional methods. The scale of operations for FIA allows for the routine analysis of minor and trace analytes and for macro-, meso-, and microsamples. The ability to work with microliter injection volumes is useful when the sample is scarce. Conventional methods of analysis, however, may allow the determination of smaller concentrations of analyte. 

The procedure of simultaneous extracting-spectrophotometric determination of nitrophenols in wastewater is proposed on the example of the analysis of mixtures of mono-, di-, and trinitrophenols. The procedure consists of extraction concentrating in an acid medium, and sequential back-extractions under various pH. Such procedures give possibility for isolation o-, m-, p-nitrophenols, a-, P-, y-dinitrophenols and trinitrophenol in separate groups. Simultaneous determination is carried out by summary light-absorption of nitrophenol-ions. The error of determination concentrations on maximum contaminant level in natural waters doesn t exceed 10%. The peculiarities of application of the sequential extractions under fixed pH were studied on the example of mixture of simplest phenols (phenol, o-, m-, />-cresols). The procedure of their determination is based on the extraction to carbon tetrachloride, subsequent back-extraction and spectrophotometric measurement of interaction products with diazo-p-nitroaniline. 

Concentration limits of the diphosphate-ion, admissible to determination of magnesium and cobalt, manganese and cobalt, zinc and cobalt by spectrophotometric method with application of the l-(2-pyridylazo)-resorcinol (PAR) are presented. Exceeding maintenance of the diphosphate-ion higher admissible supposes a preliminary its separation on the anionite in the H+-form. The optimum conditions of cobalt determination and amount of the PAR, necessary for its full fastening are established on foundation of dependence of optical density of the cobalt complex with PAR from concentration Co + and pH (buffer solutions citrate-ammoniac and acetate-ammoniac). 

Application of IP and NCS in conjunction with specification tolerance limits enables to substantiate acceptance criteria for linear regression metrological characteristics (residual standard deviation, correlation coefficient, y-intercept), accuracy and repeatability. Acceptance criteria for impurity influence (in spectrophotometric assay), solution stability and intermediate precision are substantiated as well. 

Clearly the accurate measurement of the final (infinity time) instrument reading is necessary for the application of the preceding methods, as exemplified by Eq. (2-52) for the spectrophotometric determination of a first-order rate constant. It sometimes happens, however, that this final value cannot be accurately measured. Among the reasons for this inability to determine are the occurrence of a slow secondary reaction, the precipitation of a product, an unsteady instrumental baseline, or simply a reaction so slow that it is inconvenient to wait for its completion. Methods have been devised to allow the rate constant to be evaluated without a known value of in the process, of course, an estimate of A is also obtainable. 

O Connor and Cox and Yates have reviewed the many acidity function scales. A major use of acidity functions is for the measurement of the strengths of very weak bases. The procedure utilizes spectrophotometric measurements of the concentration ratio Cb/cbh+ in solutions of known acidity function and application of Eq. (8-89). One problem is the estimation of the spectra of the pure forms (protonated and unprotonated) of the base, for the spectra are subject to the medium effect, and corrections must be applied. Another problem is that the base... 

In cases where it proves impossible to find a suitable indicator (and this will occur when dealing with strongly coloured solutions) then titration may be possible by an electrometric method such as conductimetric, potentiometric or amperometric titration see Chapters 13-16. In some instances, spectrophotometric titration (Chapter 17) may be feasible. It should also be noted that ifit is possible to work in a non-aqueous solution rather than in water, then acidic and basic properties may be altered according to the solvent chosen, and titrations which are difficult in aqueous solution may then become easy to perform. This procedure is widely used for the analysis of organic materials but is of very limited application with inorganic substances and is discussed in Sections 10.19-10.21. 

In any colorimetric determination the exact procedure will be governed partly by the particular instrument to be employed and partly by the nature of the substance which is being determined. There are nevertheless certain general principles which are universally applicable and these are also relevant to spectrophotometric determinations in general. 

Objective Evaluation of Color. In recent years a method has been devised and internationally adopted (International Commission on Illumination, I.C.I.) that makes possible objective specification of color in terms of equivalent stimuli. It provides a common language for description of the color of an object illuminated by a standard illuminant and viewed by a standard observer (H). Reflectance spectro-photometric curves, such as those described above, provide the necessary data. The results are expressed in one of two systems the tristimulus system in which the equivalent stimulus is a mixture of three standard primaries, or the heterogeneous-homogeneous system in which the equivalent stimulus is a mixture of light from a standard heterogeneous illuminant and a pure spectrum color (dominant wave-length-purity system). These systems provide a means of expressing the objective time-constant spectrophotometric results in numerical form, more suitable for tabulation and correlation studies. In the application to food work, the necessary experimental data have been obtained with spectrophotometers or certain photoelectric colorimeters. 

The study of carbonate complexes of Pu is complicated by various experimental difficulties. The low solubility of many carbonates (7), leaving a very dilute Pu concentration in solution, results in difficulties to the experiments with electrochemical or spectrophotometric methods. However, the radiometric method with solvent extraction or solubility measurement is easily applicable for the purpose. Unlike the solution with anions, like Cl, N03 etc., the concentration of which can be varied at a constant pH, the preparation of solutions with varying carbonate concentration accompanies indispensably the change of pH of the solution. As a result, the formation of carbonate complexes involves accordingly the hydrolysis reactions of Pu ions in solutions under investigation. It is therefore prerequisite to know the stability constants of Pu(IV) hydroxides prior to the study of its carbonate complexation. 

Schwing-Weill, M.J. and Wechsler, S., Spectrophotometric study of carminic acid in solution application to its determination, Analysis, 14, 290, 1986. 

The probe molecules of greatest historical interest in catalysis are the Hammett indicators [13]. The difficulty of making reliable visual or spectrophotometric observations of the state of protonation of these species on solids is well known. We have recently carried out the first NMR studies of Hanunett indicators on solid acids [ 14]. This was also the occasion of the first detailed collaboration between the authors of this article, and theoretical methods proved to strongly compliment the NMR experiments. The Hanunett story is told after first reviewing the application of theoretical chemistry to such problems. Central to the application of any physical method in chemistry is the process of modeling the relationship between the observables and molecular structure. However often one does this, it is rarely an exact process. One can rationalize almost any trend in isotropic chemical shift as a function of some variation in molecular structure - after the fact, but the quantitative prediction of such trends in advance defies intuition in most nontrivial cases. Even though the NMR spectrum is a function... 

A fully automated instrumental procedure has been developed for analyzing residual corrosion inhibitors in production waters in the field. The method uses ultraviolet (UV) and fluorescence spectrophotometric techniques to characterize different types of corrosion inhibitors. Laboratory evaluations showed that fluorescence is more suitable for field application because errors from high salinity, contamination, and matrix effect are minimized in fluorescence analysis. Comparison of the automated fluorescence technique with the classic extraction-dye transfer technique showed definite advantages of the former with respect to ease, speed, accuracy, and precision [1658],... 

Identification of dyes on dyed textiles is traditionally carried out by destructive techniques [493], TLC is an outstanding technique for identification of extracted dyestuffs and examination of inks. Figure 4.9 shows HPTLC/SERRS analysis of acridine orange [492], Wright et al. [494] have described a simple and rapid TLC-videodensitometric method for in situ quantification of lower halogenated subsidiary colours (LHSC) in multiple dye samples. The results obtained by this method were compared with those obtained by an indirect TLC-spectrophotometric method and those from HPLC. The total time for the TLC-videodensitometric assay of five standards and four samples applied to each plate was less than 45 min. The method is applicable for use in routine batch-certification analysis. Loger et al. [495,496] have chromatographed 19 basic dyes for PAN fibres on alumina on thin-layer with ethanol-water (5 2) and another 11 dyes on silica gel G with pyridine-water... 

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