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Radioactive chains

Uranium and thorium are the first members of natural radioactive chain which makes their determination in natural materials interesting from geochemical and radioecological aspect. They are quantitatively determined as elements by spectrophotometric method and/or their radioisotopes by alpha spectrometry. It is necessary to develop inexpensive, rapid and sensitive methods for the routine researches because of continuous monitoring of the radioactivity level. [Pg.214]

A chemical method for determining number-average molecular weights involves an analysis of end groups. If the polymer was prepared in such a way that each chain has either one or two labelled ends, then analysis for these ends is equivalent to counting the chains. For example, the ends could be hydroxyl groups or radioactive initiator fragments, and the analysis could involve titration, spectroscopy, or measurements of radioactivity. Chains formed in condensation polymerizations, from A-B monomers... [Pg.10]

Consider a process, such as nuclear flssion, that operates in a way so that P atoms of the first member of the chain are formed per unit time. The production and decay scheme, and assumed initial conditions for the radioactive chain, are... [Pg.38]

Sometimes the daughter of a radioactive nucleus may also be radioactive and decay to a third radioactive nucleus. Thus, a radioactive chain... [Pg.107]

The factor J has been introduced because only half of the radioactive chains have odd masses. The energy of the second disintegration is... [Pg.433]

Again, this equation is most likely to be fulfilled for the light fragment. Even in this case and even under the most optimistic assumption which we used (that all the disintegration energy which produced the A,Z nucleus remain in it) we obtain Zq—Z>2. This shows that if a delayed neutron is emitted by a nucleus near the end of a radioactive chain, the fluctuations around the smooth mass formulae must be quite large to make this possible. ... [Pg.435]

Radioactivity was discovered (1896) from observations of radioactivity occurring in natural radioactive chains. There are other instances of natural radioactivity, such as and... [Pg.668]

The natural radioactive chains are represented in O Figs. 13.1-13.4. The relative intensities of various decay modes given in those figures do not show the full precision of current information. See the appendix Table of Nuclides by R. B. Firestone for current values. [Pg.668]

The fission product which has an important effect on the short-term behavior of the reactor is Xe. The direct fractional yield of this isotope from fission is only some 0.3 %, and most of it is in fact derived from the radioactive chain shown below ... [Pg.118]

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... [Pg.1181]

The analysis of steady-state and transient reactor behavior requires the calculation of reaction rates of neutrons with various materials. If the number density of neutrons at a point is n and their characteristic speed is v, a flux effective area of a nucleus as a cross section O, and a target atom number density N, a macroscopic cross section E = Na can be defined, and the reaction rate per unit volume is R = 0S. This relation may be appHed to the processes of neutron scattering, absorption, and fission in balance equations lea ding to predictions of or to the determination of flux distribution. The consumption of nuclear fuels is governed by time-dependent differential equations analogous to those of Bateman for radioactive decay chains. The rate of change in number of atoms N owing to absorption is as follows ... [Pg.211]

The Natural Reactor. Some two biUion years ago, uranium had a much higher (ca 3%) fraction of U than that of modem times (0.7%). There is a difference in half-hves of the two principal uranium isotopes, U having a half-life of 7.08 x 10 yr and U 4.43 x 10 yr. A natural reactor existed, long before the dinosaurs were extinct and before humans appeared on the earth, in the African state of Gabon, near Oklo. Conditions were favorable for a neutron chain reaction involving only uranium and water. Evidence that this process continued intermittently over thousands of years is provided by concentration measurements of fission products and plutonium isotopes. Usehil information about retention or migration of radioactive wastes can be gleaned from studies of this natural reactor and its products (12). [Pg.222]

A scram causes the control rods to drop into the core, absorb neutrons and stop the chain reaction. Some rods perform both controlling and scram functions. The control rods are raised to increase the neutron flux (and power) or lowered to reduce it by magnetic jacks (W and CE) or a magnetic "clamshell" screw (B W). The chemical volume and control system (CVCS - not siiown) controls the water quality, removes radioactivity, and varies the reactivity by controUing the amount of a boron compound that is dissolved in the water - called a "poison." Thus, a PWR coiiirols reactivity two ways by the amount of poison in the water and by moving the control rods. [Pg.208]

Because dideoxynucleotides lack 3 -OH groups, these nucleotides cannot serve as acceptors for 5 -nucleotide addition in the polymerization reaction, and thus the chain is terminated where they become incorporated. The concentrations of the four deoxynucleotides and the single dideoxynucleotide in each reaction mixture are adjusted so that the dideoxynucleotide is incorporated infrequently. Therefore, base-specific premature chain termination is only a random, occasional event, and a population of new strands of varying length is synthesized. Four reactions are run, one for each dideoxynucleotide, so that termination, although random, can occur everywhere in the sequence. In each mixture, each newly synthesized strand has a dideoxynucleotide at its 3 -end, and its presence at that position demonstrates that a base of that particular kind was specified by the template. A radioactively labeled dNTP is included in each reaction mixture to provide a tracer for the products of the polymerization process. [Pg.358]

The extensive industrial and commercial utilization of water-soluble polymers (polyelectrolytes) in water treatment has been developed based on the charge along the polymer chains and the resultant water solubility. The use of water-soluble polymers in water treatment has been investigated by several authors [5-26] in the recovery of metals radioactive isotopes, heavy metals, and harmful inorganic residues. This allows recycling water in the industrial processes and so greatly saves... [Pg.119]

In studying two-component polymerization catalysts, beginning with Feldman and Perry (161), a radioactive label was introduced into the growing polymer chain by quenching the polymerization with tritiated alcohols. The use of these quenching agents is based on the concept of the anionic coordination mechanism of olefin polymerization occurring... [Pg.195]

The heart of the nuclear reactor boiler plant system is the reactor core, in which the nuclear fission process takes place. Nuclear fission is the splitting of a nucleus into two or more separate nuclei. Fission is usually by neutron particle bombardment and is accompanied by the release of a very large amount of energy, plus additional neutrons, other particles, and radioactive material. The generation of new neutrons during fission makes possible a chain reaction process and the subsequent... [Pg.61]

Thus, for the investigation of buried polymer interfaces, several techniques with molecular resolution are also available. Recently NMR spin diffusion experiments [92] have also been applied to the analysis of a transition zone in polymer blends or crystals and even the diffusion and mobility of chains within this layer may be analyzed. There are still several other techniques used, such as radioactive tracer detection, forced Rayleigh scattering or fluorescence quenching, which also yield valuable information on specific aspects of buried interfaces. They all depend very critically on sample preparation and quality, and we will discuss this important aspect in the next section. [Pg.378]

Stanley G. Thompson joined my group on October 1, 1942 and it fell to his lot to discover the process that was chosen for use at Clinton Laboratories (in Tennessee) and the Hanford Engineer Works (in the state of Washington) for the separation of plutonium from uranium and the immense intensity of radioactive fission products with which it was produced in the nuclear chain reactors. Again I turn to my journal to tell the story ... [Pg.25]


See other pages where Radioactive chains is mentioned: [Pg.6]    [Pg.35]    [Pg.29]    [Pg.335]    [Pg.74]    [Pg.109]    [Pg.6]    [Pg.35]    [Pg.29]    [Pg.335]    [Pg.74]    [Pg.109]    [Pg.487]    [Pg.155]    [Pg.129]    [Pg.236]    [Pg.236]    [Pg.443]    [Pg.451]    [Pg.313]    [Pg.315]    [Pg.37]    [Pg.170]    [Pg.93]    [Pg.357]    [Pg.478]    [Pg.1256]    [Pg.865]    [Pg.878]    [Pg.880]    [Pg.41]    [Pg.267]    [Pg.963]    [Pg.289]    [Pg.290]    [Pg.392]    [Pg.160]   
See also in sourсe #XX -- [ Pg.173 , Pg.192 , Pg.237 ]




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