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Colorants analytical characteristics

Possible shapes of photometric titration curves are shown in Fig. 15. Curve A is typical of the titration where the titrant alone absorbs and where the absorbance readings are taken at the wavelength of the titrant. Curve B is characteristic of systems where the product of the reaction absorbs, and curve C is typical for reactions where the analyte is converted to a non-absorbing product. When a colored analyte is converted to a colorless product by a colored titrant, curves similar to D are obtained. [Pg.3767]

Analytical Characteristics of All Classes, Sorts, Types, and Sub-groups of Caramel Colors ... [Pg.209]

Valcarcel and co-workers proposed in 2003 an automatic system for the determination of riboflavin in lyophilized food products using a solid-phase extraction process that included columns filled with cotton or silica C18 for the sequential retention of synthetic colorants and natural colorants, respectively (Gonzalez et al. 2003). In this case riboflavin was assessed as an authorized natural colorant for total estimation of this class of compounds. The analytical characteristics of this methodology are summarized in Table 18.3. [Pg.307]

Analytical and Test Methods. An aqueous solution of sodium thiosulfate forms a white precipitate with hydrochloric acid and evolves sulfur dioxide gas which is detected by its characteristic odor. The white precipitate turns yellow, iadicatiug the presence of sulfur. The addition of ferric chloride to sodium thiosulfate solutions produces a dark violet color which quickly disappears. [Pg.30]

All the alkali metals have characteristic flame colorations due to the ready excitation of the outermost electron, and this is the basis of their analytical determination by flame photometry or atomic absorption spectroscopy. The colours and principal emission (or absorption) wavelengths, X, are given below but it should be noted that these lines do not all refer to the same transition for example, the Na D-line doublet at 589.0, 589.6 nm arises from the 3s — 3p transition in Na atoms formed by reduction of Na+ in the flame, whereas the red line for lithium is associated with the short-lived species LiOH. [Pg.75]

A simple, reliable, and fast method of determining the pH of a solution and of monitoring a titration is with a pH meter, which uses a special electrode to measure H 0+ concentration. An automatic titrator monitors the pH of the analyte solution continuously. It detects the stoichiometric point by responding to the characteristic rapid change in pH (Fig. 11.9). Another common technique is to use an indicator to detect the stoichiometric point. An acid-base indicator is a water-soluble organic dye with a color that depends on the pH. The sudden change in pH... [Pg.581]

Tracer materials are defined as any product included in the test substance that can be recovered analytically for determining the drift from the application. This may be the active ingredient in an actual tank mix, or it may be a material added to the tank mix for subsequent detection. The selection of an appropriate tracer for assessing deposition rates in the field is critical to the success of a field study. Tracer materials such as low-level active ingredient products, colored dyes, fluorescent dyes, metallic salts, rare earth elements and radioactive isotopes have been used with varying degrees of success in the field. An appropriate tracer should have the following characteristics ... [Pg.976]

Soils develop by the action of the soil forming factors on soil parent materials including material transported by different agents. The result of these soil forming factors is the formation of soil horizons, different colors, and peds. Each of these factors has a pronounced effect on a soil s chemistry. Knowledge of the soil type and profile description can provide the soil chemist, analyst, or researcher with valuable information about the characteristics of soil relevant to the development of extraction, analytical, and instrumental analytical procedures. It also is the place to start when investigating the failure of a procedure. [Pg.59]

Analytical Methods. The samples were analyzed by standard AACC (21) procedures for moisture (air-oven method), protein (Method 46-13), crude fat (Method 30-25), crude fiber (Method 32-10), insoluble dietary fiber (Method 32-20) and ash (600°C, 3 hr). Starch content was determined by the polarimeter method (Method 76-20) and total sugars by Method 80-60. Color characteristics of the dried products were evaluated with the Hunter Color Difference Meter. [Pg.183]

Part—I has three chapters that exclusively deal with General Aspects of pharmaceutical analysis. Chapter 1 focuses on the pharmaceutical chemicals and their respective purity and management. Critical information with regard to description of the finished product, sampling procedures, bioavailability, identification tests, physical constants and miscellaneous characteristics, such as ash values, loss on drying, clarity and color of solution, specific tests, limit tests of metallic and non-metallic impurities, limits of moisture content, volatile and non-volatile matter and lastly residue on ignition have also been dealt with. Each section provides adequate procedural details supported by ample typical examples from the Official Compendia. Chapter 2 embraces the theory and technique of quantitative analysis with specific emphasis on volumetric analysis, volumetric apparatus, their specifications, standardization and utility. It also includes biomedical analytical chemistry, colorimetric assays, theory and assay of biochemicals, such as urea, bilirubin, cholesterol and enzymatic assays, such as alkaline phosphatase, lactate dehydrogenase, salient features of radioimmunoassay and automated methods of chemical analysis. Chapter 3 provides special emphasis on errors in pharmaceutical analysis and their statistical validation. The first aspect is related to errors in pharmaceutical analysis and embodies classification of errors, accuracy, precision and makes... [Pg.539]

Color reactions are chemical reactions that produce colored products. Identification of a compound, or more commonly a group of compounds, by color reactions is one of the oldest and simplest methods in analytical chemistry. It is based on the fact that a specific compound or a group of compounds, when treated by an appropriate reagent (often called color reagent ), produce a color that is characteristic of this compound or group of compounds. [Pg.41]

Solutions of isolated dioxiranes, characteristically dimethyldioxirane (DMD) in acetone, possess a pale yellow color, which serves as a convenient analytical index for monitoring the dioxirane consumption in oxidation reactions and kinetic studies. For DMD, the absorption maximum (n-jt transition ) centers at ca 325 nm, with a molar extinction coefficient (e) of 12.5 0.5 M cm in acetone. The alternative and more rigorous analytical method for dioxirane quantification utilizes iodometry (Kl/starch). [Pg.1134]

In most metallic solutions the two prussiates occasion precipitates of a characteristic color, which renders them of great importance in analytical chemistry, especially in qualitetlve analyses, In these reactions, the metal in solution takes the place of the potassium, and the resulting products are a soluble salt of potassa, and a double cyanide of iron and of the metal in solution, which, being usually Insoluble, is precipitated. [Pg.451]

Correlation of Structure with Source. Allochthonous-derived DOM (8) was isolated from the Suwannee River at its origin in the Okefe-nokee Swamp in southern Georgia. The fiilvic acid fraction, which is responsible for the black coloration of the water, was extensively characterized (9). Several average molecular models based on quantitative analytical data were presented in that report (10) to denote the mixture characteristics of fiilvic acid. One model, modified to depict biochemical sources and based on quantitative analytical data (10), is presented in Structure 1. Other models of Suwannee River fulvic acid (based on lignins, terpenoids, tannins, and flavonoid sources) were previously proposed (II). [Pg.200]

TNT forms charge-transfer, or 7r, complexes with polycyclic aromatic hydrocarbons, aromatic amines, and aromatic nitro compds a number of these are listed below in Table 2. The complexes with three amines (diphenylamine, diethyl-aniline, p-anisidine) have characteristic colors this forms the basis for a rapid and convenient thin-layer chromatographic analytical procedure (Ref 34) for the identification of very small amounts of TNT. (For a discussion of the many color reactions of TNT, and of composite expls containing it, see Vol 3, C405-L ff)... [Pg.750]

In chemically based selectivity, the sensing information is usually obtained from the color reaction between the analyte X and the indicator molecule I forming a colored complex X I, in which either the indicator and/or the conjugate have characteristic absorption... [Pg.291]


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See also in sourсe #XX -- [ Pg.47 , Pg.206 , Pg.209 , Pg.210 , Pg.211 , Pg.212 ]




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