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Radiotracer

A development project has been initiated with the aim of providing a radiotracer method that ultimately can be implemented as a routine calibration method for permanently installed multiphase flowmeters. The project is supported by a research grant from the Danish Ministry of Energy. [Pg.1056]

Figure 4. Principle for radiotracer leak detection in pipelines. Figure 4. Principle for radiotracer leak detection in pipelines.
Marcus P, Teissier A and Oudar J 1984 The influence of sulfur on the dissolution and the passivation of a nickel-iron alloy. 1. Electrochemical and radiotracer measurements Corrosion Sc . 24 259... [Pg.954]

Horanyi G and Rizmayer E M 1984 Radiotracer study of anion adsorption at silver electrodes in acidic medium J. Electroanal. Chem. 176 339-48... [Pg.2756]

AH components of the reaction mixture, whatever their source, are subject to the same kind of radical attacks as the starting substrate(s). Any free-radical oxidation is inevitably a cooxidation of substrate(s) and products. The yields of final products are deterrnined by two factors (/) how much is produced in the reaction sequence, and (2) how much product survives the reaction environment. By kinetic correlations and radiotracer techniques, it is... [Pg.335]

Synthetic chemical approaches to the preparation of carbon-14 labeled materials iavolve a number of basic building blocks prepared from barium [ CJ-carbonate (2). These are carbon [ C]-dioxide [ CJ-acetjlene [U— C]-ben2ene, where U = uniformly labeled [1- and 2- C]-sodium acetate, [ C]-methyl iodide, [ C]-methanol, sodium [ C]-cyanide, and [ CJ-urea. Many compHcated radiotracers are synthesized from these materials. Some examples are [l- C]-8,ll,14-eicosatrienoic acid [3435-80-1] inoxn. [ CJ-carbon dioxide, [ting-U— C]-phenyhsothiocyanate [77590-93-3] ftom [ " CJ-acetjlene, [7- " C]-norepinephrine [18155-53-8] from [l- " C]-acetic acid, [4- " C]-cholesterol [1976-77-8] from [ " CJ-methyl iodide, [l- " C]-glucose [4005-41-8] from sodium [ " C]-cyanide, and [2- " C]-uracil [626-07-3] [27017-27-2] from [ " C]-urea. All syntheses of the basic radioactive building blocks have been described (4). [Pg.438]

The nonquantitative detection of radioactive emission often is required for special experimental conditions. Autoradiography, which is the exposure of photographic film to radioactive emissions, is a commonly used technique for locating radiotracers on thin-layer chromatographs, electrophoresis gels, tissue mounted on sHdes, whole-body animal sHces, and specialized membranes (13). After exposure to the radiolabeled emitters, dark or black spots or bands appear as the film develops. This technique is especially useful for tritium detection but is also widely used for P, P, and 1. [Pg.439]

Other methods of sensitive detection of radiotracers have been developed more recently. Eourier transform nmr can be used to detect (nuclear spin 1/2), which has an efficiency of detection - 20% greater than that of H. This technique is useful for ascertaining the position and distribution of tritium in the labeled compound (14). Eield-desorption mass spectrometry (fdms) and other mass spectral techniques can be appHed to detection of nanogram quantities of radiolabeled tracers, and are weU suited for determining the specific activity of these compounds (15). [Pg.439]

Protection of the environment from uncontroHed radioactive release is also a consideration in the use of radiotracers. The quantity and concentration of radionucHdes that may be discharged into sewer systems is limited by regulations of the Nuclear Regulatory Commission (NRC). [Pg.439]

Radiotracers have also been used extensively for the quantitative rnicrodeterrnination of blood semm levels of hormones (qv), proteins, neurotransmitters, and other physiologically important compounds. Radioimmunoassay, which involves the competition of a known quantity of radiolabeled tracer, usually I or H, with the unknown quantity of semm component for binding to a specific antibody that has been raised against the component to be deterrnined, is used in the rnicro deterrnination of physiologically active materials in biological samples (see Immunoassay). [Pg.440]

Isotope Dilution Assay. An isotope dilution assay for biotin, based on the high affinity of avidin for the ureido group of biotin, compares the binding of radioactive biotin and nonradio active biotin with avidin. This method is sensitive to a level of 1—10 ng biotin (82—84), and the radiotracers typically used are p C]biotin (83), [3H]biotin (84,85) or an I-labeled biotin derivative (86). A variation of this approach uses I-labeled avidin (87) for the assay. [Pg.33]

Interdiffusion of bilayered thin films also can be measured with XRD. The diffraction pattern initially consists of two peaks from the pure layers and after annealing, the diffracted intensity between these peaks grows because of interdiffusion of the layers. An analysis of this intensity yields the concentration profile, which enables a calculation of diffusion coefficients, and diffusion coefficients cm /s are readily measured. With the use of multilayered specimens, extremely small diffusion coefficients (-10 cm /s) can be measured with XRD. Alternative methods of measuring concentration profiles and diffusion coefficients include depth profiling (which suffers from artifacts), RBS (which can not resolve adjacent elements in the periodic table), and radiotracer methods (which are difficult). For XRD (except for multilayered specimens), there must be a unique relationship between composition and the d-spacings in the initial films and any solid solutions or compounds that form this permits calculation of the compo-... [Pg.209]

Fowler, J S, Wolf, A P The Synthesis of Carbon-II, Fluorine 18 and Nitrogen 13 Labeled Radiotracers for Biomedical Applications, Mono graph NAS-NS-3601, Technical Information Center, U S Department of Energy... [Pg.167]

Whereas in many metals with relatively simple and isotropic crystal structures the parameter / has values between 0.5 and 1, it can have much more extreme values in materials in which the mobile species move through much less isotropic structures with 1-D or two-dimensional (2-D) channels, as is often the case with insertion reaction electrode materials. As a result, radiotracer experiments can provide misleading information about self-diffusion kinetics in such cases. [Pg.367]

Group 2 Radiotracer pulsed field gradient NMR measurements (PFG NMR) ... [Pg.511]

The effect on the eyes was more noticeable. A single application of the solution mentioned above produced moderate redness and short and minor swelling of conjunctiva. Radiotracer studies with Hostapur SAS [102] revealed that after oral (up to 50 mg/kg) and dermal application on rats, the product and its metabolites were very quickly excreted either in completely oxidized form as carbon dioxide or in the urine and feces. Residues in organs and tissues after 7 days were well below 1 ppm. [Pg.215]

A variety of other techniques have been used to investigate ion transport in conducting polymers. The concentrations of ions in the polymer or the solution phase have been monitored by a variety of in situ and ex situ techniques,8 such as radiotracer studies,188 X-ray photoelectron spectroscopy (XPS),189 potentiometry,154 and Rutherford backscatter-ing.190 The probe-beam deflection method, in which changes in the density of the solution close to the polymer surface are monitored, provides valuable data on transient ion transport.191 Rotating-disk voltammetry, using an electroactive probe ion, provides very direct and reliable data, but its utility is very limited.156,19 193 Scanning electrochemical microscopy has also been used.194... [Pg.580]

A correlation between the amount of adsorbed ions and the electrode potential, in particular E. , has been identified apparently for the first time by Frumkin and Obrutschewa [26Fru]. A minimum of ionic adsorption was found at E, this is equivalent to the absence of specific adsorption at Ep c- The measurement of the amount of adsorbed ions was performed by measuring the ionic concentration in the solution as a function of the electrode potential or by measuring the surface concentration of adsorbed ions by e.g. radiotracer techniques (see also 4.2). (Data obtained with this method are labelled lA). [Pg.186]


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Radiotracers

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