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Radiation chemistry solution

Detailed studies on radiation chemistry of PEO have been performed [74-77]. Upon y-irradiation, the gel-dose drops abruptly along with an increase in the concentration and molecular weight of the polymer, thus reaching values of 0.15-0.25 Mrad in the range of practical interest [75]. Oxygen is a strong inhibitor and when it is carefully removed from the solution, crosslinking of PEO occurs at doses as low as 0.01 Mrad [76]. [Pg.108]

This definition of electrochemistry disregards systems in which nonequilibrium charged species are produced by external action in insulators for example, by electric discharge in the gas phase (electrochemistry of gases) or upon irradiation of liquid and sohd dielectrics (radiation chemistry). At the same time, electrochemistry deals with certain problems often associated with other fields of science, such as the structure and properties of sohd electrolytes and the kinetics of ioific reactions in solutions. [Pg.739]

Phillips, G.O. and Moody, G.J. (1960a). Radiation chemistry of carbohydrates. Part IV. The effect of gamma-radiation on aqueous solutions of sucrose. J. Chem. Soc. 155, 762-768. [Pg.21]

Allen, A. O. (1961), The Radiation Chemistry oj Water and Aqueous Solutions, Van Nostrand, Princeton, N.J. [Pg.192]

G. Czapski, Radiation chemistry of oxygenated aqueous solutions. Ann. Rev. Phys. Chem. 22, 171—208 (1971). [Pg.201]

When radiolysing a solution, the radiation interacts mainly with solvent molecules, since the solution consists mainly of the latter and the radiation interacts with the molecules unselectively. Consequently, the radiation chemistry of a solution is the combination of the production of initial intermediates from the solvent, which will be the same as in pure solvents, and the reaction of those intermediates with the solute. [Pg.327]

Allen, A.O. In The Radiation Chemistry of Water and Aqueous Solutions, D. Van Nostrand Princeton, 1961. [Pg.8]

While many of the important reactions in radiation and photochemistry are fast, not all are diffusion-limited. The random flight simulation methodology has been extended to include systems where reaction is only partially diffusion-controlled or is spin-controlled [54,55]. The technique for calculating the positions of the particles following a reflecting encounter has been described in detail, but (thus far) this improvement has not been incorporated in realistic diffusion kinetic simulations. Random flight techniques have been successfully used to model the radiation chemistry of aqueous solutions [50] and to investigate ion kinetics in hydrocarbons [48,50,56-58]. [Pg.91]

The irradiation of water is immediately followed by a period of fast chemistry, whose short-time kinetics reflects the competition between the relaxation of the nonhomogeneous spatial distributions of the radiation-induced reactants and their reactions. A variety of gamma and energetic electron experiments are available in the literature. Stochastic simulation methods have been used to model the observed short-time radiation chemical kinetics of water and the radiation chemistry of aqueous solutions of scavengers for the hydrated electron and the hydroxyl radical to provide fundamental information for use in the elucidation of more complex, complicated chemical, and biological systems found in real-world scenarios. [Pg.92]

Radiation chemistry highlights the importance of the role of the solvent in chemical reactions. When one radiolyzes water in the gas phase, the primary products are H atoms and OH radicals, whereas in solution, the primary species are eaq , OH, and H" [1]. One can vary the temperature and pressure of water so that it is possible to go continuously from the liquid to the gas phase (with supercritical water as a bridge). In such experiments, it was found that the ratio of the yield of the H atom to the hydrated electron (H/eaq ) does indeed go from that in the liquid phase to the gas phase [2]. Similarly, when one photoionizes water, the threshold energy for the ejection of an electron is much lower in the liquid phase than it is in the gas phase. One might suspect that a major difference is that the electron can be transferred to a trap in the solution so that the full ionization energy is not required to transfer the electron from the molecule to the solvent. [Pg.159]

There has been continued interest in the radiation chemistry of the purines since early reports on oriented DNA by Graslund et al. [35] which suggest that the main trapping site of one-electron oxidation in DNA is the guanine base. It is remarkable that in aqueous solution, the electron adducts of the purine nucleosides and nucleotides undergo irreversible protonation at carbon with a rate constant 2 orders of magnitude higher than that for carbon protonation of the electron adduct in thymidine [36]. It is therefore important to know the properties of the various purine reduction products and to ask why they have not been observed in irradiated DNA. [Pg.442]

The previous section outlined the typical e loss and e gain products observed in the nucleic acid bases in the solid state. These studies can be applied to the study of the radiation chemistry of DNA. The relevance of the study of model systems is shown by considering the following remarkable observations. Years ago, Ehrenberg et al. showed the EPR spectra of the 5,6-dihydrothymine-5-yl radical observed in thymine, thymidine, and DNA. The spectra are nearly identical [46]. The reduction product observed in cytosine monohydrate is the N3 protonated anion. In solution, this reduction product gives rise to a 1.4-mT EPR doublet. The same feature is present in irradiated DNA at 77 K. Likewise, the result of e loss in guanine bases is characterized by a broad EPR singlet. The same feature is also evident in the EPR spectrum of DNA irradiated and observed at 77 K. [Pg.443]

Because of the multivalent nature of the actinide ions, understanding the radiation-induced change of the valence-state of the actinide in solutions under self-irradiation or external irradiation is a challenge in radiation chemistry. Some of the ions are strong a-emitters. It is also important from a practical viewpoint that the solution chemistry of actinide ions is closely related to the storage and the repository of the wastes. Much work combined with experiment and simulation has been conducted and reviews were summarized [136,140-144]. [Pg.715]

Although the radiation-induced oxidation of ethanol has been fully in-- vestigated (2, 22, 23), little work has been published on the oxidation of other alcohols. In connection with a project concerned with the relative rates of hydroxyl radical reactions using 2-propanol as reference solute, it was thought desirable first to investigate the radiation chemistry of 2-propanol-oxygen solutions both in aqueous solution and pure 2-propa-nol. The results of this investigation are presented here. [Pg.114]

Finally, the National Institute of Standards and Technology (NIST) in the United States has several chemical kinetics databases that are available for purchase from the Office of Standard Reference Data at NIST. The NIST Standard Reference Data Base 17 gives gas-phase rate constants through 1993 and Data Base 40 gives solution-phase data through 1992. In addition, aqueous-phase data are available through the Radiation Chemistry Data Center of the Notre Dame Radiation Laboratory (http //www.rcdc.nd.edu/). [Pg.173]


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See also in sourсe #XX -- [ Pg.603 ]




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Solution chemistry

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