Simultaneous Determination

The equilibrium ratios are not fixed in a separation calculation and, even for an isothermal system, they are functions of the phase compositions. Further, the enthalpy balance. Equation (7-3), must be simultaneously satisfied and, unless specified, the flash temperature simultaneously determined. 

Bain A D and Duns G J 1994 Simultaneous determination of spin-lattioe (T1) and spin-spin (T2) relaxation times in NMR a robust and faoile method for measuring T2. Optimization and data analysis of the offset-saturation experiment J. Magn. Reson. A 109 56-64... 

Several melting points can be simultaneously determined the substances must of course be placed in separate minute heaps in the constant temperature area on the surface of the apparatus. 

Blanco and co-workers" reported several examples of the application of multiwavelength linear regression analysis for the simultaneous determination of mixtures containing two components with overlapping spectra. For each of the following, determine the molar concentration of each analyte in the mixture. 

Eerguson, G. K. Quantitative HPLG Analysis of a Psychotherapeutic Medication Simultaneous Determination of Amitriptyline Hydrochloride and Perphenazine, /. Chem. Educ. 1998, 75, 1615-1618. 

Pandey, S. McHale, M. E. R. Horton, A. M. et al. Kinetics-Based Indirect Spectrophotometric Method for the Simultaneous Determination of Mn04 and Gt207 ,... 

Direct multi-element or multi-component simultaneous determination of ultra-trace matter in samples of environmental concern. 

A novel sensitive and seleetive adsorptive stripping proeedure for simultaneous determination of eopper, bismuth and lead is presented. The method is based on the adsorptive aeeumulation of thymolphetalexone (TPN) eomplexes of these elements onto a hanging mereury drop eleetrode, followed by reduetion of adsorbed speeies by voltammetrie sean using differential pulse modulation. The optimum analytieal eonditions were found to be TPN eoneentration of 4.0 p.M, pH of 9.0, and aeeumulation potential at -800 mV vs. Ag/AgCl with an aeeumulation time of 80 seeonds. The peak eurrents ai e proportional to the eoneentration of eopper, bismuth and lead over the 0.4-300, 1-200 and 1-100 ng mL ranges with deteetion limits of 0.4, 0.8 and 0.7 ng mL respeetively. The proeedure was applied to the simultaneous determination of eopper, bismuth and lead in real and synthetie samples with satisfaetory results. 

SIMULTANEOUS DETERMINATION OF ORGANIC COMPOUNDS IN MIXTURE USING THE SUBSEQUENT EXTRACTIONS... 

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. 

The simultaneous determination of Co and Ni is also made at pH 8 in the presence of pyrophosphate. The EDTA is added to the mixture of coloured complexes of these metals to bind the Cu and Zn admixtures into the inactive complexes. The optical density of the solution is measured at 530, 555 and 580 nm. The solution is heated to the boiling point to destmct the complex formed by Ni with PAR, and then is cooled. Again the measurements of optical density ai e performed at the same wavelengths. The Ni concentration is calculated from the variation in the optical density, and the Co concentration is calculated from the final values of optical density. The detection limits for these metals are 4 and 2 p.g/dm, respectively. 

Significant practical objective in analytical chemistry is control on contents of metal ions in various objects including natural. Effective method for practical uses is one of simultaneous determination of content of various metals in object, because it decreases time of analysis, quantity of reagents and probe. 

SIMULTANEOUS DETERMINATION OF LEVONORGESTREL AND ETHINYL ESTRADIOL IN LOW-DOSE ORAL CONTRACEPTIVES BY HPTLC-DENSITOMETRY... 

SIMULTANEOUS DETERMINATION OF ACETYL SALICYLIC ACID AND ACETAMINOPHEN IN A.C.A TABLETS BY FT-IR/ATR SPECTROMETRY... 

Since the 1950s XRF has been used extensively for the analysis of solids, powders, and liquids. The technique was extended to analyze thin-film materials in the 1970s. XRF can be used routinely for the simultaneous determination of elemental composition and thickness of thin films. The technique is nondesuuctive, rapid, precise, and potentially very accurate. The results are in good agreement with other elemental analysis techniques including wet chemical, electron-beam excitation techniques, etc. 

The principle application of XRF thin-film analysis is in the simultaneous determination of composition and thickness. The technique has been used for the routine analysis of single-layer films since 1977 and multiple-layer films since 1986. Two main sources of publications in the fields are the annual volumes of Advances in X-Ray Analysis by Plenum Press, New York, and the Journal of X-Ray Spectrometry by Heyden and Sons, London. Typical examples on the analysis of single-layer films and multiple-layer films are used to illustrate the capabilities of the technique. 

Aoun, M., Plasari, E., Davis, R. and Villenuaux, I., 1999. A simultaneous determination of nucleation and growth rates from batch spontaneous precipitation. Chemical Engineering Science, 54, 1161-1180. 

A thin-layer chromatography assay was developed for ffie simultaneous determination of the three major hydroxylated metabolites of antipyrine 409,410, and 411 in urine of humans and other animals (82JPP168) (Scheme 95). 

Figure 5.3 Analysis of 100 ml of (a) surface water and (b) drinking water sample spiked with 0.1 pig/ml of microcystins, using column-switching HPLC 1, microcystin-RR 2, microcystin-YR 3, microcystin-LR. Reprinted from Journal of Chromatography A, 848, H. S. Lee et al, On-line trace enrichment for the simultaneous determination of microcystins in aqueous samples using high performance liquid chromatography with diode-array detection , pp 179-184, copyright 1999, with permission from Elsevier Science.

H. S. Eee, C. K. Jeong, H. M. Eee, S. J. Choi, K. S. Do, K. Kim and Y. H. Kim, On-line trace emicliment foi the simultaneous determination of microcystins in aqueous samples using high peifoi mance liquid cliromatography with diode-aixay detection , /. Chromatogr. 848 179-184 (1999). 

T. Seki, K. Yamaji, Y. Orita, S. Moriguchi and A. Sliinoda, Simultaneous determination of uric acid and creatinine in biological fluids by column-switching liquid cliromatogra-phy with ulti aviolet detection , 7. Chromatogr. A 730 139-145 (1996). 

H. Zehender, J. Denouel, M. Roy, E. Ee Saux and P. Schaub, Simultaneous determination of terbinafine (Eamisil) and five metabolites in human plasma and urine by liigh-peifoimance liquid cliromatogi aphy using on-line solid-phase exti action , 7. Chromatogr. B 664 347-355 (1995). 

Simultaneous Determination of Tafei Slopes and Corrosion Rates from Rp Determinations... 

To obtain reliable, accurate, and reproducible methods for quantitative estimation of deoxy sugars, certain conditions must be fulfilled. Thus, it is necessary that the chromogen be formed quantitatively from the sugar. The chromogen must then react quantitatively with the compound used for color formation, and lastly, the dye, once formed, should be stable and have a well defined molar extinction coefficient. In methods in which all of these conditions are not or cannot be fulfilled, recourse must be had to simultaneous determinations with suitable standard substances, a requirement not always easy to fulfil. 

The shift of the half-wave potentials of metal ions by complexation is of value in polarographic analysis to eliminate the interfering effect of one metal upon another, and to promote sufficient separation of the waves of metals in mixtures to make possible their simultaneous determination. Thus, in the analysis of copper-base alloys for nickel, lead, etc., the reduction wave of copper(II) ions in most supporting electrolytes precedes that of the other metals and swamps those of the other metals present by using a cyanide supporting electrolyte, the copper is converted into the difficultly reducible cyanocuprate(I) ion and, in such a medium, nickel, lead, etc., can be determined. 

The above considerations will be illustrated by the simultaneous determination of manganese and chromium in steel and other ferro-alloys. The absorption spectra of 0.001 M permanganate and dichromate ions in 1M sulphuric acid, determined with a spectrophotometer and against 1M sulphuric acid in the reference cell, are shown in Fig. 17.20. For permanganate, the absorption maximum is at 545 nm, and a small correction must be applied for dichromate absorption. Similarly the peak dichromate absorption is at 440 nm, at which permanganate only absorbs weakly. Absorbances for these two ions, individually and in mixtures, obey Beer s Law provided the concentration of sulphuric acid is at least 0.5M. Iron(III), nickel, cobalt, and vanadium absorb at 425 nm and 545 nm, and should be absent or corrections must be made. 

HJ. Kisner, C.W. Brown, GJ. Kavamos, "Simultaneous Determination of Triglycerides, Phospholipids, and Cholesteryl Esters by Infrared Spectrometry", Anal. Chem. 1982 (54) 1479-1485. 

Sulfur, and tetraethyllead, simultaneous determination by modified differential absorptiometry, 144, 145 determination by x-ray emission spectrography, 66, 67, 329 in biological samples, determination by monochromatic x-ray absorption-edge method, 299-301 in hydrocarbons, determination by monochromatic absorptiometry, 130-135... 

The simultaneous determination of a great number of constants is a serious disadvantage of this procedure, since it considerably reduces the reliability of the solution. Experimental results can in some, not too complex cases be described well by means of several different sets of equations or of constants. An example would be the study of Wajc et al. (14) who worked up the data of Germain and Blanchard (15) on the isomerization of cyclohexene to methylcyclopentenes under the assumption of a very simple mechanism, or the simulation of the course of the simplest consecutive catalytic reaction A — B —> C, performed by Thomas et al. (16) (Fig. 1). If one studies the kinetics of the coupled system as a whole, one cannot, as a rule, follow and express quantitatively mutually influencing single reactions. Furthermore, a reaction path which at first sight is less probable and has not been therefore considered in the original reaction network can be easily overlooked. 

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