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Reagent, radioactive

See Immunoassay Medical diagnostic reagents Radioactive elements. [Pg.442]

There are many potential advantages to kinetic methods of analysis, perhaps the most important of which is the ability to use chemical reactions that are slow to reach equilibrium. In this chapter we examine three techniques that rely on measurements made while the analytical system is under kinetic rather than thermodynamic control chemical kinetic techniques, in which the rate of a chemical reaction is measured radiochemical techniques, in which a radioactive element s rate of nuclear decay is measured and flow injection analysis, in which the analyte is injected into a continuously flowing carrier stream, where its mixing and reaction with reagents in the stream are controlled by the kinetic processes of convection and diffusion. [Pg.622]

Historically, the Redox process was used to achieve the same purification as in the Purex process (97,129). The reagents were hexone (methyl isobutyl ketone) as the solvent, dichromate as an oxidant, and A1(N02)3 as the salting agent. The chief disadvantages of hexone are its flammability and its solubihty in water. However, because A1(N03)3 collects in the highly radioactive waste, thereby impeding the latter s further processing, the Redox process was abandoned in favor of the Purex process. [Pg.201]

Radioactive tracers account for about 20% of the worldwide market for consumables and reagents for life science research. In 1994 the value was estimated at about 300 million. The principal fuU line manufacturers are Du Pont—NEN Research Products (Boston, Massachusetts) and Amersham International (Amersham, U.K.). These companies share roughly equaHy about 85% of the radiochemicals worldwide market. In addition to an extensive line of catalog products, these suppHers offer custom labeling and custom synthesis services. The rest of the market is shared by producers of a limited range of products or services, such as ICN Biomedicals (Costa Mesa, California) and American Radiolabeled Chemicals (St. Louis, Missouri). [Pg.439]

Metallacarboranes. These are used in homogeneous catalysis (222), including hydrogenation, hydrosilylation, isomerization, hydrosilanolysis, phase transfer, bum rate modifiers in gun and rocket propellants, neutron capture therapy (254), medical imaging (255), processing of radioactive waste (192), analytical reagents, and as ceramic precursors. [Pg.254]

Nuclear methods which include a variety of radioactive elements as in organic reagents, complexes or salts. [Pg.2]

Many fluorinations by electropositive fluorine reagents produce a-fluoro carbonyl compounds as the final result An extensive review exists on the preparation of a-fiuorocarbonyl compounds [101 Also, electropositive reagents are used widely in the preparation of F-labeled radioactive materials required in positron etmssion tomography for biomedical research Excellent reviews are available on fluonne-18 labeling [//, 72]. [Pg.133]

The chemistry of xenon is much more extensive than that of any other noble gas. Only one binary compound of krypton. KrF2, has been prepared. It is a colorless solid that decomposes at room temperature. The chemistry of radon is difficult to study because all its isotopes are radioactive. Indeed, the radiation given off is so intense that it decomposes any reagent added to radon in an attempt to bring about a reaction. [Pg.190]

After the addition of the non-radioactive material, the labeled material is added to the mixture and the mixture allowed to proceed toward equilibriim. In equilibrium analysis the order of addition of reagents is not critical as long as sufficient time is allowed for establishing equilibrium of the complete mixture (3,4). [Pg.59]

In Chapter 7, approaches for visualization of zones in chromatograms are discussed, including use of nondestructive and destructive dyeing reagents, fluorescence quenching on layers with a fluorescent indicator, and densitometry. In Chapter 8, additional detection methods, such as those used for biologically active and radioactive zones, as well as the recovery of separated, detected zones by scraping and elution techniques are covered. [Pg.9]

Compounds that are radioactive can be located on a preparative layer by contact film autoradiography, electronic autoradiography, and storage phosphor screen imaging [21-23]. These methods differ in terms of factors such as simplicity, speed, sensitivity, and resolution, and the method of choice depends on the available equipment, reagents, and instrumentation. All are nondestructive, and the detected compounds can be recovered without change for later studies. [Pg.180]

For an active ingredient in a radioactive drug product, except for nonradioactive reagent kits, the reserve sample shall be retained for ... [Pg.57]

One curious observation, however, was that pure U actually had a lower radioactivity than natural U compounds. To investigate this. Curie synthesized one of these compounds from pure reagents and found that the synthetic compound had a lower radioactivity than the identical natural example. This led her to believe that there was an impurity in the natural compound which was more radioactive than U (Curie 1898). Since she had already tested all the other elements, this impurity seemed to be a new element. In fact, it turned out to be two new elements—polonium and radium— which the Curies were successfully able to isolate from pitchblende (Curie and Curie 1898 Curie et al. 1898). For radium, the presence of a new element was confirmed by the observation of new spectral lines not attributable to any other element. This caused a considerable stir and the curious new elements, together with their discoverers, achieved rapid public fame. The Curies were duly awarded the 1903 Nobel prize in Physics for studies into radiation phenomena, along with Becquerel for his discovery of spontaneous radioactivity. Marie Curie would, in 1911, also be awarded the Nobel prize in chemistry for her part in the discovery of Ra and Po. [Pg.663]

Many of the reagents developed initially for the recovery of base or radioactive metals have also been investigated as potential PGM extractants, e.g., phosphine oxides,310-313 dialkylsulfoxides,314 dialkyl-and diphemd-thioureas,296,315-317 thiopicolinamides, thiobenzanilide,319 phosphate diesters,320 tetra-... [Pg.790]

Figure 1.11 Tyrosine residues are subject to nucleophilic and electrophilic reactions. The unprotonated phe-nolate ion may be alkylated or acylated using a variety of bioconjugate reagents. Its aromatic ring also may undergo electrophilic addition using diazonium chemistry or Mannich condensation, or be halogenated with radioactive isotopes such as 12iI. Figure 1.11 Tyrosine residues are subject to nucleophilic and electrophilic reactions. The unprotonated phe-nolate ion may be alkylated or acylated using a variety of bioconjugate reagents. Its aromatic ring also may undergo electrophilic addition using diazonium chemistry or Mannich condensation, or be halogenated with radioactive isotopes such as 12iI.

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See also in sourсe #XX -- [ Pg.43 ]




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Experiments with radioactive reagents

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