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JAEA Reports

The Dissolving Test of the Uranium Oxide using Amide System Extraction Solvent

Mizuno, Mineo*; Kosaka, Yuji*; Mori, Yukihide*; Shimada, Takashi*

JNC TJ8410 2004-006, 85 Pages, 2004/03

JNC-TJ8410-2004-006.pdf:3.05MB

/The process (the UPRISE method) of dissolving uranium and plutonium selectively and separating from oxide fuel using the amide system extraction solvent have been investigated. By the cold test which used Nd oxide so far, the dissolving of Nd with about 0.2 mol to the solvent of 250mL is confirmed. In this work, the investigations of the dissolving tendency of uranium to the amide system extraction solvent and decontamination factor (DF) of the typical fission product (FP) such as Nd were carried out, and following results are obtained. (1)In the test of the same dissolving conditions, the uranium dissolving rate to extraction solvent DOBA was approximately equivalent to the case of the DOiBA. (2)Three kinds of extraction solvent were examined in the same dissolving condition, the difference of the uranium dissolving rate was observed. The results of the dissolving rates indicated the order of NN'-hexyl-2, ethyl-hexan-amid-1.6 mol/L nitric acid complex $$>$$ NN'-dibutyl-butyl-amid-1.7 mol/L nitric acid complex $$>$$ NN'-di-isobutyl-isobutyl-amid-1.5 mol/L nitric acid complex. (3)In the case of DOBA extraction solvent, the dissolving rate increased by about 2 order with the increase of the nitric acid concentration from 1mol/L up to 3.5mol/L and strong influence of the nitric acid concentration was confirmed to the dissolving rate. (4)In the tests with the NN'-dibutyl-butyl-amid-1.7 mol/L nitrie acid complex and NN'-di-isobutyl-isobutyl-amid-1.5 mol/L nitric acid complex, the DF values of Zr, Ru and Ce increased with the elapse of the test duration and exceeded 100 after 150 hours of test duration. On the other hand, the DF value indicated around 1 for Sr, Mo and Pd, and around 0.1 for Nd. (5)In the test with the NN'-hexyl-2-ehyl-hexan-amid-1.6 mol/L nitric acid complex, significant difference wasn't observed in the tendency of the elapsed change among the DF values of the FP elements. The DF values of all FP elements except Nd and Pd exceeded 100 after 100 ...

Journal Articles

Direct Extraction of Uranium and Plutonium from Oxide Fuel using TBP-HNO$$_{3}$$Complex for Super-DIREX Process

Kamiya, Masayoshi; Miura, Sachiko; Nomura, Kazunori; Koyama, Tomozo; Ogumo, Shinya*; Mori, Yukihide*; Enokida, Yoichi*

CD-ROM, P1-35, 4P., 4 Pages, 2004/00

Super-DIREX is a new reprocessing method which has high economical efficiency. Experimental study of this process was started on the direct extraction of U and Pu from irradiated MOX fuel by the supercritical carbon dioxide (SFCO$$_{2}$$) containing TBP-HNO$$_{3}$$ complex. This report describes direct extraction of U and Pu with TBP-HNO3 complex at atmospheric pressure, as the first test for irradiated fuel, in order to investigate the applicability of SFCO$$_{2}$$ containing TBP-HNO$$_{3}$$ complex. In this test, dependency on dissolution temperature, Pu content, fuel/ TBP-HNO$$_{3}$$ complex ratio and effect of voloxidation were investigated. From these results, TBP-HNO$$_{3}$$ complex was found to be effective in the respect of the recovery of U and Pu. The number of the process step in dissolution and co-extraction is small, and amount of waste can be reduced. It is applicable to the direct extraction in Super-DIREX.

JAEA Reports

Research on Plant of Metal Fuel Fabrication using Casting Process

Senda, Yasuhide*; Mori, Yukihide*

JNC TJ9420 2004-004, 192 Pages, 2003/12

JNC-TJ9420-2004-004.pdf:8.79MB

This document presents the plant concept of metal fuel fabrication system (38tHM/y) using casting process in electrolytic recycle,which based on recent studies of its equipment design and quality control system. And we estimate the cost of its construction and operation, including costs of maintenance, consumed hardware and management of waste.

JAEA Reports

Dissolution of uranium oxide TBP-HNO$$_{3}$$ complex

Mori, Yukihide*; Shimada, Takashi*; Kosaka, Yuji*; Mizuno, Mineo*

JNC TJ8400 2003-013, 69 Pages, 2002/12

JNC-TJ8400-2003-013.pdf:3.53MB

As a head end process for the pulverization of the spent fuel, the mechanical method (the shredder method) and the pyro-chemical method (oxidization heat-treatment) have been examined. UO$$_{2}$$ is a main ingredient of Uranium oxide powder by the mechaical method, and U$$_{3}$$O$$_{8}$$ is that by the pyro-chemical method. Moreover, the particle size of the pulverized powder depend on the conditions of the pulverizing process. As it was considered that the difference of dissolution rates of samples was caused by the difference of sample chemical forms and dissolution temperature, parametric surveys on chemical form and particle size of powder and dissolution temperature were carried out, and the following results were obtained. (1)The remarkable difference of dissolution rate between U$$_{3}$$3O$$_{8}$$ powder(average particle size 3.7$$mu$$m) and UO$$_{2}$$ powder (average particle size 2.4$$mu$$m) which have comparatively similar particle size was not observed. (2)It was confirmed that the dissolution rate became lower according to the particle size increase (average particle size 2.4$$mu$$m$$sim$$1mm) And it was considered that dissolution rate had strong dependency on particle size, according to the results that the powder with 1mm particle size did not dissolute completely after 5 hours test. (3)The temperature dependency of the dissolution rate was confirmed by dissolution test with UO$$_{2}$$ powder (average particle size 2.4$$mu$$m $$sim$$ 1mm). The higher dissolution rate was obtained in the higher dissolution temperature, and 11 kcal/mol was obtained as activation energy of dissolution. (4)In the dissolution test of UO$$_{2}$$ powder, the nitric acid concentration started to change earlier than that of U$$_{3}$$O$$_{8}$$ powder and concentration change range became larger compared with that in the dissolution test of U$$_{3}$$O$$_{8}$$ powder. It was considered that those differences were caused by difference in mole ratio of Uranium and nitric acid which are consumed in the ...

Oral presentation

Latest situation and future targets of radiation countermeasures around water and woods environments in a priority investigation area on radioactive materials contamination

Iimoto, Takeshi*; Maedera, Ikuhiko*; Nunokawa, Jun*; Matsuzawa, Hajime*; Kurokawa, Sumihiko*; Yanagawa, Yukihide*; Someya, Seiichi*; Hashimoto, Makoto; Seya, Natsumi; Okawa, Yasuhisa; et al.

no journal, , 

no abstracts in English

Oral presentation

Fuel and NFBC assemblies design for the next generation sodium-cooled fast reactor, 1; The Conceptual design for the upper structure of fuel assembly

Ozawa, Takayuki; Maeda, Seiichiro; Hayakawa, Satoshi*; Mori, Yukihide*

no journal, , 

The upper structure of fuel assembly for the next generation sodium-cooled fast reactor, including the method of dissimilar connection between wrapper tube and handling head and the structure of the upper shield, was conceptually designed to fulfill functional requirements within a tentative limit of temperature to use wrapper tube material, based on the result of computational fluid dynamics (CFD) analysis.

Oral presentation

Report from fast reactor strategic roadmap committee, 2; Long-term perspective: Significance of fast reactor development

Mori, Yukihide*; Ono, Kiyoshi; Ohtaki, Akira

no journal, , 

no abstracts in English

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