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Chemical analytical determinations

The results showed that while none of the books stored in the clean Welsh environment had deteriorated to any significant extent, nearly all the volumes subjected to London s acidic pollution exhibited evidence of decay, some within less than 10 years. In addition, the superior ageing properties of leathers prepared with hydrolysable tannins were confirmed. Of the various chemical analytical determinations undertaken, the only results to show any correlation with the degree of deterioration observed were those for the number of -terminal amino acid groups on the protein. This figure reflects the amount by which the collagen polypeptide chain had been broken and was considered to be evidence for hydrolytic deterioration. [Pg.113]

Another important area of analytical chemistry, which receives some attention in this text, is the development of new methods for characterizing physical and chemical properties. Determinations of chemical structure, equilibrium constants, particle size, and surface structure are examples of a characterization analysis. [Pg.9]

In the recent years intensive studies related to modification of silica with organic compounds of various chemical nature have being conducted in order to concentrate selectively metal ions from solutions and then to perform their analytical determination directly in the sorbent phase, or after that, to elute with appropriate reagents in solution. [Pg.277]

In the present work, the technique of XO and MTB immobilization onto silica gel in the form of its complexes with Fe(III) and Bi(III) respectively were found. The acid - base and chemical-analytical characteristics of solid-phase reagents were examined. The optimal conditions of quantitative recovery of Pb(II) and Zn(II) from diluted solutions, such as acidity of aqueous phase, the mass of the sorbents, the volume of solutions and the time of equilibrium reaching, were found. The methods of and F" detenuination were based on a competitive reactions of Zr(IV) with immobilized MTB and or F". Optimal conditions of 0,0 and F" determination in solution using SG, modified ion associates QAS-MTB (pH = 1,5, = 5-10 mol/1). [Pg.334]

In the case of coupled heterogeneous catalytic reactions the form of the concentration curves of analytically determined gaseous or liquid components in the course of the reaction strongly depends on the relation between the rates of adsorption-desorption steps and the rates of surface chemical reactions. This is associated with the fact that even in the case of the simplest consecutive or parallel catalytic reaction the elementary steps (adsorption, surface reaction, and desorption) always constitute a system of both consecutive and parallel processes. If the slowest, i.e. ratedetermining steps, are surface reactions of adsorbed compounds, the concentration curves of the compounds in bulk phase will be qualitatively of the same form as the curves typical for noncatalytic consecutive (cf. Fig. 3b) or parallel reactions. However, anomalies in the course of bulk concentration curves may occur if the rate of one or more steps of adsorption-desorption character becomes comparable or even significantly lower then the rates of surface reactions, i.e. when surface and bulk concentration are not in equilibrium. [Pg.13]

The chemical properties of the alkylarylsulfonates are used in its analytical determination. As anions, LAS and other anionic surfactants react with large cations to salts, which are soluble in organic solvents (e.g., CHC13). By analysis it can be seen that cations such as Hyamine 1622 (25) and methylene blue, which rearrange with LAS to complex (26), are widely spread. These reactions are the basis for the so-called two-phase titration, an extensively used method... [Pg.86]

In recent years micellar solutions of sodium dodecyl sulfate are being used increasingly in analytical determinations, chemical reactions, and catalysis. [Pg.274]

As AOS is a mixture of different chemical species, determination of its composition by modern analytical techniques is perhaps even more important than for most other surfactants this chapter therefore also describes the state of the art of the analysis of AOS. The chapter also contains a brief review of the biodegradability and the toxicity of AOS. [Pg.365]

Often, the chemist tends to report Here is the process. These are the starting materials and reaction conditions. The product is obtained (analytically determined) with a good yield. Let the engineers deal with the rest of it from now on . This attitude may cause serious damages and losses. Until the chemist himself is confident that all the chemical, technological and economic aspects of the developed process meet the required criteria, his work is not finished. ... [Pg.197]

In order to define this variety of food matrices, chemical composition differences that primarily influence chemical analytical measurements have to be considered. Major food components determining basic chemical make-up are the proximate composition of fat, protein, carbohydrate, ash, and moisture. Variations in ash content in general have a minor influence on analytical methods for other constituents and impact of moisture content can be controlled. Thus the major components influencing analytical performance are the relative levels of fat, protein, and carbohydrate. [Pg.211]

Method validation is needed to demonstrate the acceptability of the analytical method. A recovery test on a chemical being determined should be performed in order to verify the reliability of the series of analyses. Recovery studies are usually conducted by spiking untreated sediment with the target chemical at the deteetion limit, quantitation limit and in the range of 10-50 times the detection limit. The method is considered acceptable when the recoveries typically are greater than 70%. When the recovery is less than 70%, an improvement in the analytical methods is needed. Where this is not possible for technical reasons, then lower recovery levels may be acceptable provided that method validation has demonstrated that reproducible recoveries are obtained at a lower level of recovery. Analysis is usually done in duplicate or more, and the coefficient of variation (CV) should be less than 10% to ensure that recoveries will be consistently within the range 70-110%. [Pg.904]

The Henry s law constant is essentially an air-water partition coefficient which can be determined by measurement of solute concentrations in both phases. This raises the difficulty of accurate analytical determination in two very different media which usually requires different techniques. Accordingly, effort has been devoted to devising techniques in which concentrations are measured in only one phase and the other concentration is deduced from a mass balance. These methods are generally more accurate. The principal difficulty arises with hydrophobic, low-volatility chemicals which can establish only very small concentrations in both phases. [Pg.13]

In 1962, Parker and Hatchard described a photoelectric spectrometer for phosphorescence measurements with which they were capable of obtaining phosphorescence spectra, and of determining lifetimes and quantum efficiencies of a large number of organic compounds. This work stimulated intensely the interest in the phosphorimetry of diverse chemical analytes [5], and one year later, Wine-... [Pg.10]

A copolymer is a macromolecule comprising two chemically distinct types of monometer unit, A and B, whilst a terpolymer is composed of units A, B and C. The analytically determined composition of a copolymer is expressed as the weight fractions WA and WB of its constituents. For LS studies on a copolymer solution it is necessary to know the value of the specific refractive index increment v, which can be either measured or calculated from ... [Pg.212]

In Analytical Chemistry. one of the oldest and most objective scientific disciplines, the current impetus for research comes from the needs of other disciplines and from society s need to protect itself and the environment from noxious chemicals. Analytical chemistry uses a large number of physical, chemical and biochemical principles to determine whether a particular, potentially noxious substance, the analyte, is part of specific, commercially useful and societally important matrices of substances (e.g.. [Pg.242]

Uses Intermediate in the manufacture of azo dyes and pigments for printing inks, textiles, paints, plastics, and crayons curing agent for isocyanate-terminated polymers and resins rubber compounding ingredient analytical determination of gold formerly used as chemical intermediate for direct red 61 dye. [Pg.405]

Principally the same, but chemically simpler, sequence was used to prepare arylnitro anion-radicals from arylamines, in high yields. For instance, aqueous sodium nitrite solution was added to a mixture of ascorbic acid and sodium 3,5-dibromo-4-aminobenzenesulfonate in water. After addition of aqueous sodium hydroxide solution, the cation-radical of sodium 3,5-dibromo-4-nitro-benzenesulfonate was formed in the solution. The latter was completely characterized by its ESR spectrum. Double functions of the nitrite and ascorbic acid in the reaction should be underlined. Nitrite takes part in diazotization of the starting amine and trapping of the phenyl a-radical formed after one-electron reduction of the intermediary diazo compound. Ascorbic acid produces acidity to the reaction solution (needed for diazotization) and plays the role of a reductant when the medium becomes alkaline. The method described was proposed for ESR analytical determination of nitrite ions in water solutions (Lagercrantz 1998). [Pg.211]

Electrochemistry can be broadly defined as the study of charge-transfer phenomena. As such, the field of electrochemistry includes a wide range of different chemical and physical phenomena. These areas include (but are not limited to) battery chemistry, photosynthesis, ion-selective electrodes, coulometry, and many biochemical processes. Although wide ranging, electrochemistry has found many practical applications in analytical measurements. The field of electroanalytical chemistry is the field of electrochemistry that utilizes the relationship between chemical phenomena which involve charge transfer (e.g. redox reactions, ion separation, etc.) and the electrical properties that accompany these phenomena for some analytical determination. This new book presents the latest research in this field. [Pg.141]

While the use of soft surfaces would seem to be mandated by the foregoing discussion of bounce-off problems, there are a number of disadvantages to coating the impactor surfaces with a substance such as grease. For example, it makes accurate mass determinations difficult and can introduce such a large background of certain chemicals that the chemical analysis of these elements in the particles becomes difficult. In addition, with such surfaces one cannot use chemical analytical techniques that only probe the upper surface layer because the coating surrounds some of the collected particles. [Pg.611]

Chemical analytical methods used in veterinary drug residue depletion studies in target animals constitute a potential source of suitable methods for determining compliance of tissue residues with established MRLs. In some situations. [Pg.419]

The chemical analytical data on which Table I and Figures 2-5 are based were determined by the Analytical Chemistry Section of the Illinois State Geological Survey. The Survey research reported is sponsored, in part, by Grant No. R-800059 and Contract No. 68-02-0246 from the U. S. Environmental Protection Agency, Demonstration Projects Branch, Control Systems Laboratory, Research Triangle Park, N. C. [Pg.26]

The accuracy of any of the above-mentioned methods of analytically determining the rate of propagation of a deflagration wave depends finally on the validity of the rate laws used, and on the values of the physical constants of the gases under consideration. In particular, the activation energy, and steric factor for any combustible are very important parameters. Much work is being done on the kinetics of chemical reactions, so that more accurate data on reaction rates will be available. It is hoped that this work will lead to better agreement between theoretical and experimental results. [Pg.78]


See other pages where Chemical analytical determinations is mentioned: [Pg.444]    [Pg.132]    [Pg.75]    [Pg.132]    [Pg.312]    [Pg.93]    [Pg.60]    [Pg.112]    [Pg.128]    [Pg.912]    [Pg.152]    [Pg.6]    [Pg.36]    [Pg.11]    [Pg.47]    [Pg.212]    [Pg.228]    [Pg.236]    [Pg.415]    [Pg.168]    [Pg.231]    [Pg.259]    [Pg.272]    [Pg.88]    [Pg.12]    [Pg.333]    [Pg.263]    [Pg.397]    [Pg.14]   
See also in sourсe #XX -- [ Pg.113 ]




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Analytical determinations

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