Compounds radioactive

Narasimhan et al.(39) have confirmed the very limited, if not negligible, capacity of sperm to synthesize SGG by incubating bovine spermatozoa with labelled glycerol and galactose. No radioactivity was detected in the SGG following incubation with these compounds. Radioactivity from these compounds was, however, found to be incorporated into SGG when they were injected into the testes of mature rats. 

Table 3-2 lists important physical properties of radium and selected radium compounds. Radioactive properties of the four naturally-occurring radium isotopes are listed in Table 3-3. In addition to the naturally occurring isotopes, there are 12 other known isotopes of radium. The principal decay schemes of the uranium and thorium decay series that produce the naturally-occurring radium isotopes are presented in Figure 3-1.

Iodine Compound, Radioactive, from Thyroid Gland and Body Fluids, Chromatographic... 

BR fed to rice seedlings was rapidly converted into acidic, water-soluble compounds. Radioactivity was found in both a chloroform-soluble fraction and a water-soluble fraction in the ratio 51 49, after a 5 hr feeding period (7). 

Strontium is widely distributed in the earth s crust and oceans. Strontium is released into the atmosphere primarily as a result of natural sources, such as entrainment of dust particles and resuspension of soil. Radioactive strontium is released into the environment as a direct result of anthropogenic activities. Stable strontium can be neither created nor destroyed. However, strontium compounds may transform into other chemical compounds. Radioactive strontium is formed by nuclear reactions. Radioactive decay is the only mechanism for decreasing the concentration of radiostrontium. The half-life of 90Sr is 29 years. 

Variety of inorganic and organic compounds, radioactive materials and radionuclides... 

Iodine Compounds, Radioactive, from Thyroid Gland and Body Fluids, Chromatographic Atudysis (Roche, Lissitzky, and Michel) Ion Exchange Resins, Measurement of Complex Ion Stability by Use... 

For a radioactive compound, the molar activity (the number of radioactive disintegrations per mole per unit time, or some quantity proportional to this) is directly proportional to the ratio of radioactive to stable isotope in the compound. Radioactivity can be measured with a precision of 1% or better, depending upon how much care one is willing to take. 

Compounds, radioactively labelled in one or more positions, can be synthesised chemically. Procedures for preparation of specifically tagged organic substances are to be found in a very comprehensive monograph [467]. EURATOM [189] publishes short summaries of new work in the realm of the chemistry of labelled compounds. 

Among the most observed chemical contaminants are toxic minerals (metals, metalloids and other inorganic compounds), radioactive isotopes, mycotoxins and other microbial toxins, halo-genated organic compounds, phytotoxins as representatives of natural contaminants and others. For the selection of contaminants to be covered in this chapter, a number of criteria were taken into account, the most important of which include ... 

Used (particularly He, Ar) to provide an inert atmosphere, e.g. for welding, and in electric light bulbs, valves and discharge tubes (particularly Ne). Liquid He is used in cryoscopy. The amounts of He and Ar formed in minerals by radioactive decay can be used to determine the age of the specimen. Xe and to a lesser extent Kr and Rn have a chemistry the other noble gases do not form chemical compounds. 

Other compounds which may be found in crude oil are metals such as vanadium, nickel, copper, zinc and iron, but these are usually of little consequence. Vanadium, if present, is often distilled from the feed stock of catalytic cracking processes, since it may spoil catalysis. The treatment of emulsion sludges by bio-treatment may lead to the concentration of metals and radioactive material, causing subsequent disposal problems. 

The slightly different physical properties of deuterium allow its concentration in ordinary hydrogen (or the concentration of a deuterium-containing compound in a hydrogen compound) to be determined. Exchange of deuterium and hydrogen occurs and can be used to elucidate the mechanism of reactions (i.e. the deuterium is a non-radioactive tracer). Methanol exchanges with deuterium oxide thus ... 

Relatively little is known about the chemistry of the radioactive Group I element francium. Ignoring its radioactivity, what might be predicted about the element and its compounds from its position in the periodic table ... 

Also present in the first test tube is a synthetic analog of ATP in which both the 2 and 3 hydroxyl groups have been replaced by hydrogens This compound is called 2 3 dideoxyadenosme triphosphate (ddATP) Similarly ddTTP is added to the second tube ddGTP to the third and ddCTP to the fourth Each tube also contains a primer The primer is a short section of the complementary DNA strand which has been labeled with a radioactive isotope of phosphorus ( P) When the electrophoresis gel is examined at the end of the experiment the positions of the DNAs formed by chain extension of the primer are located by a technique called autoradiography which detects the particles emitted by the P isotope... 

Naturally occurring isotopes of any element are present in unequal amounts. For example, chlorine exists in two isotopic forms, one with 17 protons and 18 neutrons ( Cl) and the other with 17 protons and 20 neutrons ( Cl). The isotopes are not radioactive, and they occur, respectively, in a ratio of nearly 3 1. In a mass spectrum, any compound containing one chlorine atom will have two different molecular masses (m/z values). For example, methyl chloride (CH3CI) has masses of 15 (for the CH3) plus 35 (total = 50) for one isotope of chlorine and 15 plus 37 (total = 52) for the other isotope. Since the isotopes occur in the ratio of 3 1, molecular ions of methyl chloride will show two molecular-mass peaks at m/z values of 50 and 52, with the heights of the peaks in the ratio of 3 1 (Figure 46.4). 

Special techniques for experimentation with the actinide elements other than Th and U have been devised because of the potential health ha2ard to the experimenter and the small amounts available (15). In addition, iavestigations are frequently carried out with the substance present ia very low coaceatratioa as a radioactive tracer. Such procedures coatiaue to be used to some exteat with the heaviest actinide elements, where only a few score atoms may be available they were used ia the earHest work for all the transuranium elements. Tracer studies offer a method for obtaining knowledge of oxidation states, formation of complex ions, and the solubiHty of various compounds. These techniques are not appHcable to crystallography, metallurgy, and spectroscopic studies. 

OtherApphca.tlons. Many appHcations of adsorption involving radioactive compounds simply parallel similar appHcations involving the same compounds in nonradio active forms, eg, radioactive carbon-14, or deuterium- or tritium-containing versions of CO2, H2O, hydrocarbons. For example, molecular sieve 2eohtes are commonly employed for these separations, just as for the corresponding nonradio active uses. 

Fluorine, which does not occur freely in nature except for trace amounts in radioactive materials, is widely found in combination with other elements, accounting for ca 0.065 wt % of the earth s cmst (4). The most important natural source of fluorine for industrial purposes is the mineral fluorspar [14542-23-5] CaF2, which contains about 49% fluorine. Detailed annual reports regarding the worldwide production and reserves of this mineral are available (5). A more complete discussion of the various sources of fluorine-containing minerals is given elsewhere (see Fluorine compounds, inorganic). 

ImmunO lSS iy. Chemiluminescence compounds (eg, acridinium esters and sulfonamides, isoluminol), luciferases (eg, firefly, marine bacterial, Benilla and Varela luciferase), photoproteins (eg, aequorin, Benilld), and components of bioluminescence reactions have been tested as replacements for radioactive labels in both competitive and sandwich-type immunoassays. Acridinium ester labels are used extensively in routine clinical immunoassay analysis designed to detect a wide range of hormones, cancer markers, specific antibodies, specific proteins, and therapeutic dmgs. An acridinium ester label produces a flash of light when it reacts with an alkaline solution of hydrogen peroxide. The detection limit for the label is 0.5 amol. 

Performance assessments are predictions of radioactivity releases, the rate of transfer of contaminants through various media, and the potential for hazard to the pubHc. These are based on a combination of experimental data obtained in the process called site characterization and detaded computations about radionuchdes and their effects. The progressive attack on the metal or ceramic waste container, the diffusion of water into the waste form, the leaching of the radioactive compounds, diffusion out, and washing away of radionuchdes are all considered. 

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