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Program - Brookhaven National Laboratory

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Deuteron breakup reactions have recently caught considerable attention in association with not only the<br />

development of neutron sources, such as those used in the International Fusion Materials Irradiation Facility<br />

(IFMIF) and Accelerator Driven Systems (ADS), but also the study of projectile breakup of exotic and halo<br />

nuclei. Although neutron production from inclusive (d,xn) reaction is essentially important in the design<br />

of neutron sources, inclusive (d,xp) reactions are also helpful to understand the mechanism of deuteron<br />

breakup reactions and have an advantage that the experimental data are more available than (d,xn)<br />

data. Deuteron induced reactions on many nuclei are studied by using the modified Glauber model with<br />

trajectory modifications on Coulomb and nuclear interactions. The total deuteron and proton reaction<br />

cross sections are calculated down to the threshold energy and compared with experimental data and<br />

optical model calculations. Then, the modified Glauber model is incorporated into a model calculation for<br />

analyses of nucleon production from deuteron breakup reactions, in which the elastic breakup process and<br />

the inelastic breakup process are described by the continuum discretized coupled-channels method and the<br />

Glauber model, respectively. In addition to these two direct processes, the evaporation and pre-equilibrium<br />

processes are described by the Hauser-Feshbach theory and the Exiton model. Target mass number and<br />

incident energy dependences on deuteron breakup reactions are investigated systematically through the<br />

present analyses.<br />

PR 90<br />

Extraction Behavior of Polonium-210 from HCl and HNO3 Solution Using Tributyl<br />

Phosphate<br />

Ali Younes, Marcel Mokili, Julie Champion, Gilles Montavon, SUBATECH laboratory (UMR 6457),<br />

IN2P3-CNRS/EMN, Nantes/Universite des Nantes, Nantes 44307, France. Cyrille Alliot, CRCNA,<br />

INSERM U892, Nantes 44007, France.<br />

A new route for the production of purified Po-210 (Polonium) was accomplished by irradiating Bi-209<br />

(Bismuth) foil for two hours by a 38 MeV alpha external beam delivered by the ARRONAX cyclotron in<br />

Nantes with an average beam current of 0.1 µA. The separation of the radiotracer of Po-210 (2.10−13 mol)<br />

from the macroscopic quantity of Bi-209 (3.10−2 mol) were performed by extraction of Po-210 to an organic<br />

phase (10% TBP in para-Xylene) from a 7M HCl solution and back-extracted to a 9M HNO3 phase after<br />

studying different parameters (TBP dilution degree, solvent , acid nature). The current investigation aimed<br />

in explaining the mechanism of extraction and back-extraction of Po-210 from hydrochloric and nitric acid<br />

respectively. In the present study, we determine the distribution ratios in solvent extraction (in tributyl<br />

phosphate-hydrochloric acid and tributyl phosphate-nitric acid systems) and the distribution coefficients<br />

in ion exchange (anionic resin AG1 X8 and cationic resin AG50 X8) at different acidic range. From these<br />

results, we discussed the polonium - chloride / nitrate complexation and the chemical species extracted<br />

and back-extracted at different acid concentration, and determined the best experimental conditions for<br />

polonium extraction. Based on our results and by comparing with previous data, we confirm the formation<br />

of a strong neutral polonium chloride complexes (HaPoCl4+a; a=0, 2) that can be extracted in tributyl<br />

phosphate, and a complete non-extraction of bismuth nuclides which have a high tendency to form anionic<br />

complexes (BiCl −2<br />

5 , or [Bi(H2O)Cl5] 2− , and BiCl6 3− ) that have high affinity toward aqueous phase. For<br />

back-extraction, our results allow us to confirm the presence of weak polonium-nitrate complexes; upon<br />

using a high concentration of nitric acid, a degradation mechanism of TBP occurred, thus releasing Po-210<br />

into the 9M HNO3 phase from the previously extracted organic phase.<br />

PR 91<br />

309

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