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Pulse radiolysis, ionic liquids

The kinetics data of the geminate ion recombination in irradiated liquid hydrocarbons obtained by the subpicosecond pulse radiolysis was analyzed by Monte Carlo simulation based on the diffusion in an electric field [77,81,82], The simulation data were convoluted by the response function and fitted to the experimental data. By transforming the time-dependent behavior of cation radicals to the distribution function of cation radical-electron distance, the time-dependent distribution was obtained. Subsequently, the relationship between the space resolution and the space distribution of ionic species was discussed. The space distribution of reactive intermediates produced by radiation is very important for advanced science and technology using ionizing radiation such as nanolithography and nanotechnology [77,82]. [Pg.288]

It seems to the present authors that the above-mentioned scheme of the initiation process in the glass matrices can be extended, at least, to the radiation-induced ionic polymerizations in liquid solutions at higher temperatures. This will be verified by rapid techniques of measurement, such as the pulse radiolysis method. [Pg.418]

Behar D, Neta P, Schultheisz C. (2002) Reaction kinetics in ionic liquids as studied by pulse radiolysis Redox reactions in the solvents methyltributylammo-nimn bis(trifluoromethylsulfonyl)imide and N-butylpyridiiun tetrafluoroborate. JPhys Chem A 106 3139-3147. [Pg.59]

Fig. 15. Benzophenone anion solvation observed at 800 nm in two ionic liquids by OFSS pulse radiolysis spectroscopy. The traces consist of three 1.5-ns OFSS segments. Fig. 15. Benzophenone anion solvation observed at 800 nm in two ionic liquids by OFSS pulse radiolysis spectroscopy. The traces consist of three 1.5-ns OFSS segments.
Yang J, Kondoh T, Norizawa K, Nagaishi R, Tagushi M, Takahashi K, Rat oh R, Anishchik SV, Yoshida Y, Tagawa S. (2008) Picosecond pulse radiolysis Dynamics of solvated electrons in ionic liquid and geminate ion recombination in liquid alkanes. Radiat Phys Chem 77 1233-1238. [Pg.156]

James R Wishart received a B.S. in Chemistry from the Massachusetts Institute of Technology in 1979 and a Ph.D. in Inorganic Chemistry from Stanford University in 1985 under the direction of Prof Henry Taube. After a postdoctoral appointment at Rutgers University, in 1987 he joined the Brookhaven National Laboratory Chemistry Department as a Staff Scientist in the Radiation Chemistry Group. He founded and presently supervises the BNL Laser-Electron Accelerator Facility for picosecond electron pulse radiolysis. His research interests include ionic liquids, radiation chemistry, electron transfer, and new technology and techniques for pulse radiolysis. He has authored over 90 papers and chapters, and is the co-editor of Advances in Chemistry Series o. 254, Photoehemistry and Radiation Chemistry. [Pg.625]

A recent study using a pulse-radiolysis technique on liquid benzene solutions has shown that there is an abundant yield of excited singlet ( B2 ) and triplet ( B) states of benzene. The effect of ionic scavengers in this study shows that ions are precursors of both singlet and triplet states. It is concluded that the excited states arise from ion-electron recombination. This recombination is particularly facile in benzene solution owing to the numerous excited states of low energy in benzene, which rapidly thermalize the electrons. The formation of excited species which are relatively unreactive, as implied by the observation of fluorescence from these states, may account for the low (7-value of benzene decomposition in the liquid phase. [Pg.131]

Grodkowski, J. and Neta, R, Reaction kinetics in the ionic liquid methyltributyl ammonium bis(trifluoromethylsulfonyl)imide. Pulse radiolysis study of CF3 radical reactions, J. Phys. Chem. A106, 5468-5473 (2002). [Pg.305]

Both investigations also reported the pulse radiolysis of solutes dissolved in ionic liquids. Behar et al. studied the effect of the presence of Oj and CCI4 in [bmim][PF6] their results suggested that the latter was a more effective radical scavenger. They also looked at the formation of the radical cations of chlorpromazine (ClPz-+) andN,N,7 r, N -tetramethyl-p-phenylenediamine (TPMD- ) in the same solvent. Finally, the kinetics of oxidation of ClPz in [bmim][PF( ] were studied. The experimentally determined bimolecular rate constant values were corrected for the high viscosity of the ionic liquid by estimation of the values of the diffusion-controlled rate constant, using Equation (5.3),... [Pg.123]

Behar, D., Gonzalez, C. Neta, P. (2001). Reaction Kinetics in Ionic Liquids Pulse Radiolysis Studies of l-Butyl-3-methylimidazolium Salts,. Phys. Ghent. A105 7607-7614. [Pg.562]


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See also in sourсe #XX -- [ Pg.5 , Pg.6 , Pg.10 ]




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