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Journal Articles

An Empirical model for the corrosion of stainless steel in BWR primary coolant

Uchida, Shunsuke*; Hanawa, Satoshi; Naito, Masanori*; Okada, Hidetoshi*; Lister, D. H.*

Corrosion Engineering, Science and Technology, 52(8), p.587 - 595, 2017/10

 Times Cited Count:4 Percentile:21.41(Materials Science, Multidisciplinary)

Based on the relationship among ECP, metal surface conditions, exposure time and other environmental conditions, a model to evaluate the ECP and corrosion rate of steel was developed by coupling a static electrochemical analysis and a dynamic oxide layer growth analysis. Major conclusion obtained on the model are as follows. The effect of H$$_{2}$$O$$_{2}$$ and O$$_{2}$$ concentrations on ECP were successfully explained as the effects of oxide layer growth. Hysteresis of ECP under changes in water chemistry conditions were successfully explained with the model. Decreases in ECP due to neutron exposure were explained well by radiation-induced diffusion in the oxide layers.

Journal Articles

Electrochemical properties of uranium(VI) complexes with multidentate ligands in $$N,N$$-dimethylformamide

Kim, S.-Y.; Asakura, Toshihide; Morita, Yasuji; Ikeda, Yasuhisa*

Journal of Alloys and Compounds, 408-412, p.1291 - 1295, 2006/02

 Times Cited Count:10 Percentile:54.65(Chemistry, Physical)

The electrochemical reactions of UO$$_{2}$$($$beta$$-diketonato)$$_{2}$$DMF, UO$$_{2}$$(trop)$$_{2}$$DMF and UO$$_{2}$$(sap)(DMF)$$_{2}$$, (DMF = N,N-dimethylformamide, $$beta$$-diketonate = thenoyltrifluoroacetonate (ttfa), benzoyltrifluoroacetonate (btfa), and dibenzoylmethanate(dbm), trop = tropolonate, and sap = 2-salicylidenaminophenolate) complexes in DMF solution containing tetrabutyl ammonium perchlorate as a supporting electrolyte have been studied with cyclic voltammetry. These uranyl(VI) complexes were found to be quasi-reversibly reduced to U(V) species. The formal redox potentials (E$$^{o}$$, ${it vs}$. ferrocene/ferrocenium) for U(VI)/U(V) couples were determined to be -1.18 V for UO$$_{2}$$(ttfa)$$_{2}$$DMF, -1.18 V for UO$$_{2}$$(btfa)$$_{2}$$DMF, -1.46 V for UO$$_{2}$$ (dbm)$$_{2}$$DMF, -1.46 V for UO$$_{2}$$(trop)$$_{2}$$DMF, and -1.59 V for UO$$_{2}$$(sap)(DMF)$$_{2}$$.

Journal Articles

Electrochemical and spectroelectrochemical behaviour of Np(VI) ions in nitric acid solutions

Kim, S.-Y.; Asakura, Toshihide; Morita, Yasuji

Radiochimica Acta, 93(12), p.767 - 770, 2005/12

 Times Cited Count:10 Percentile:56.74(Chemistry, Inorganic & Nuclear)

Electrochemical and spectroelectrochemical has been used to investigate the behaviour of Neptunium (VI) in concentration 1-8 M HNO$$_{3}$$ solutions. The electrochemical reactions of Np(VI) ions were found to occur quasi-reversibly. The formal redox potentials (E$$^{circ}$$) for Np(VI)/Np(V) couples were determined to be +0.906, +0.908, +0.909, +0.902, +0.896, +0.895, +0.888, and +0.884 V (vs. Ag/AgCl) for Np(VI) ions in 1, 2, 3, 4, 5, 6, 7, 8 M HNO$$_{3}$$ solutions, respectively. The reduction processes of Np(VI) ions were followed spectroelectrochemically by using an optical transparent thin layer electrode cell. It was found that the absorption spectra measured at the applied potentials from +1.10 to +0.60 V versus Ag/AgCl reference electrode redox couple for Np(VI) in HNO$$_{3}$$ solution have clear isosbestic points. These results indicate that the reduction product of Np(VI) is Np(V), which is considerably stable in HNO$$_{3}$$ solution.

Journal Articles

Electrochemical studies of plutonium(IV) complexes in aqueous nitrate solutions

Kim, S.-Y.; Asakura, Toshihide; Morita, Yasuji

JAERI-Conf 2005-007, p.341 - 344, 2005/08

Electrochemistry has been used to investigate the behavior of plutonium(IV) in 1-7 M HNO$$_{3}$$ solutions. These Pu(IV) complexes were found to be reduced quasi-reversibly to Pu(III) species. The formal redox potentials (E$$^{o}$$) for Pu(IV)/Pu(III) couples were determined to be +0.721, +0.712, +0.706, +0.705, +0.704, 0.694, and +0.696 V (vs. Ag/AgCl(SSE)) for Pu(IV) complexes in 1, 2, 3, 4, 5, 6, 7 M HNO$$_{3}$$ solutions, respectively. These results indicate that the reduction product of Pu(IV) is Pu(III), which is considerably stable in HNO$$_{3}$$ solution.

Journal Articles

Electrochemical behavior and some thermodynamic properties of UCl$$_4$$ and UCl$$_3$$ dissolved in a LiCl-KCl eutectic melt

Kuznetsov, S. A.*; Hayashi, Hirokazu; Minato, Kazuo; Gaune-Escard, M.*

Journal of the Electrochemical Society, 152(4), p.C203 - C212, 2005/04

 Times Cited Count:108 Percentile:94.63(Electrochemistry)

The electrochemical behavior of UCl$$_4$$ and UCl$$_3$$ dissolved in LiCl-KCl eutectic melt was studied at 723-823 K. Electroreduction of U(IV) in LiCl-KCl melt occurs via two successive steps involving transfer of one and three electrons. The diffusion coefficients of U(IV) and U(III) ions were determined by linear sweep voltammetry, chronopotentiometry, and chronoamperometry. The formal standard potential of E$$^*$$U(IV)/U(III), E$$^*$$U(IV)/U, and E$$^*$$U(III)/U were determined and some thermodynamic properties of UCl$$_4$$ and UCl$$_3$$ dissolved in LiCl-KCl eutectic melt were calculated. Influence of oxide ions on electrochemical behavior was also studied.

Journal Articles

Electrochemical redox reactions of uranium(VI) complexes with multidentate ligands in dimethyl sulfoxide

Kim, S.-Y.; Asakura, Toshihide; Morita, Yasuji; Uchiyama, Gunzo*; Ikeda, Yasuhisa*

Radiochimica Acta, 93(2), p.75 - 81, 2005/02

 Times Cited Count:9 Percentile:53.19(Chemistry, Inorganic & Nuclear)

no abstracts in English

Journal Articles

Electrochemical and spectroelectrochemical properties of neptunium(VI) ions in nitric acid solution

Kim, S.-Y.; Asakura, Toshihide; Morita, Yasuji; Uchiyama, Gunzo*; Ikeda, Yasuhisa*

Journal of Radioanalytical and Nuclear Chemistry, 262(2), p.311 - 315, 2004/11

 Times Cited Count:11 Percentile:58.51(Chemistry, Analytical)

no abstracts in English

Journal Articles

Recovery of U by electrolysis of UN in LiCl-KCl eutectic melts

Shirai, Osamu; Uozumi, Koichi*; Iwai, Takashi; Arai, Yasuo

Journal of Nuclear Science and Technology, 39(Suppl.3), p.745 - 748, 2002/11

no abstracts in English

JAEA Reports

Proceedings of the Workshop on Molten Salts Technology and Computer Simulation

Hayashi, Hirokazu; Minato, Kazuo

JAERI-Conf 2001-016, 181 Pages, 2001/12

JAERI-Conf-2001-016.pdf:11.72MB

Applications of molten salts technology to separations and syntheses of materials have been studied eagerly, which would develop new fields of materials science. Research Group for Actinides Science, Department of Materials Science, Japan Atomic Energy Research Institute (JAERI), together with Reprocessing and Recycle Technology Division, Atomic Energy Society of Japan, organized the Workshop on Molten Salts Technology and Computer Simulation at Tokai Research Establishment, JAERI on September 18, 2001. In the workshop eleven lectures were made and lively discussions were there on the bases and applications of the molten salts technology that covered the structure and basic properties of molten salts, the pyrochemical reprocessing technology and the relevant computer simulation.

Journal Articles

Dissolution and formation of nuclear materials in molten media

Ogawa, Toru; Minato, Kazuo

Pure and Applied Chemistry, 73(5), p.799 - 806, 2001/05

 Times Cited Count:15 Percentile:54.07(Chemistry, Multidisciplinary)

no abstracts in English

Oral presentation

Electrochemical behavior of neptunium in NaCl-2CsCl melt

Hayashi, Hirokazu; Minato, Kazuo*

no journal, , 

For a basis of the future nuclear fuel cycle, understanding the behavior of transuranium elements (TRU: Np, Pu, Am, Cm) is important. Experimental study on pyrochemical reprocessing of the fuels containing TRU is one of the important topics. But limited data are available on the behavior of TRU in some molten salts including NaCl-2CsCl melt which is considered to be used for pyrochemical reprocessing of MOX fuels in RIAR process. Only the electrochemical behavior of Np$$^{4+/}$$Np$$^{3+}$$ redox couple has been reported for Np ions in NaCl-2CsCl melt. In the present study, behavior of Np ions including the reduction of Np$$^{3+}$$ in NaCl-2CsCl melt was investigated. A typical cyclic voltammogram shows 2 groups of the signals corresponding to Np species. They were assigned to the redox reactions of Np$$^{3+}$$/Np and Np$$^{4+/}$$Np$$^{3+}$$, respectively by comparing with those observed in LiCl-KCl melt. The redox potentials and the diffusion coefficients obtained by various transient electrochemical techniques will be presented.

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