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Journal Articles

Examination of a new quantification method of Zr isotopes in solid samples by LA-ICP-MS for Zr-93 analysis in difficult to dissolve radioactive wastes

Morii, Shiori; Yomogida, Takumi; Asai, Shiho*; Ouchi, Kazuki; Oka, Toshitaka; Kitatsuji, Yoshihiro

KEK Proceedings 2023-2, p.132 - 137, 2023/11

New analytical method of a combination of laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) and isotope dilution mass spectrometry (IDMS) for quantification of Zr isotopes in a solid sample was investigated. Solid Zr-isotope reference was added to a simulated radioactive waste sample as a spike, then Zr isotope ratio was measured by LA-ICP-MS. As a result, we successfully quantify Zr isotopes in the simulated radioactive waste sample by new IDMS. There is a possibility that this new method can be applied for quantification of Zr-93 in difficult to dissolve radioactive wastes.

Journal Articles

Development of a quantification method for Zr isotopes in solid samples by LA-ICP-MS for rapid analysis of Zr-93 in high-level radioactive wastes

Morii, Shiori; Yomogida, Takumi; Asai, Shiho*; Ouchi, Kazuki; Oka, Toshitaka; Kitatsuji, Yoshihiro

Bunseki Kagaku, 72(10.11), p.441 - 448, 2023/10

Rapid analytical method for the determination of Zr-93 in radioactive wastes has been developed. Laser ablation (LA)-ICP-MS was applied to the analysis of Zr isotopes in simulated high-level radioactive waste (HLW). Sample preparation time was dramatically reduced by using a DGA resin as the adsorbent for Zr. Direct quantification of Zr isotopes in this resin sample was carried out by LA-ICP-MS. Laser settings were optimized to obtain a reliable isotope ratio of the sample by LA-ICP-MS. Quantification of Zr isotopes in the simulated HLW solution by isotope dilution mass spectrometry (IDMS) was examined. The amount of Zr-90 in the sample obtained by IDMS corresponded to a value calculated from the given concentration of Zr in the sample within uncertainty. Thus, this method can be applied for the quantification of Zr-93 in radioactive wastes.

Journal Articles

Uranium hydroxide/oxide deposits on uranyl reduction

Ouchi, Kazuki; Matsumura, Daiju; Tsuji, Takuya; Kobayashi, Toru; Otobe, Haruyoshi; Kitatsuji, Yoshihiro

RSC Advances (Internet), 13(24), p.16321 - 16326, 2023/05

 Times Cited Count:0 Percentile:0(Chemistry, Multidisciplinary)

We clarified the chemical state transformation of deposits following the reduction of uranyl ion (U$$^{rm VI}$$O$$_{2}$$$$^{2+}$$) from the results of electrochemical quartz crystal microbalance, impedance spectra and X-ray absorption fine structure measurements. We propose the following deposition mechanism: (1) U$$^{rm IV}$$ is formed by the disproportionation of U$$^{rm V}$$. (2) U$$^{rm IV}$$ forms U$$^{rm IV}$$ hydroxide deposits, and (3) finally, the hydroxide deposits transform into U$$^{rm IV}$$ oxide, generally having a larger electrical resistance than the former.

Journal Articles

New measurement system based on small-angle neutron scattering for structural analysis of light-responsive materials

Iwase, Hiroki*; Akamatsu, Masaaki*; Inamura, Yasuhiro; Sakaguchi, Yoshifumi*; Morikawa, Toshiaki*; Kasai, Satoshi*; Ouchi, Keiichi*; Kobayashi, Kazuki*; Sakai, Hideki*

Journal of Applied Crystallography, 56(1), p.110 - 115, 2023/02

 Times Cited Count:2 Percentile:85.44(Chemistry, Multidisciplinary)

With the increasing importance of light-responsive materials, it is vital to analyze the relationship between function and structural changes induced by light irradiation. Small-angle scattering (SAS) is effective for such structural analysis. However, quantitatively capturing local molecular structure formation and molecular reactions at a scale of less than 1 nm via SAS is difficult. In this study, to analyze the structure of non-equilibrium phenomena in light-responsive materials, a new sample environment has been developed for a time-of-flight small- and wide-angle neutron scattering instrument (TAIKAN), comprising a UV-Vis irradiation system, UV-Vis absorption measurement equipment and photodetector. Simultaneous measurement of small-angle neutron scattering and UV-Vis absorption was achieved. This system was used to demonstrate the in situ observation of UV-Vis irradiation-induced structural change of micelles formed by a light-responsive surfactant sample in an aqueous solution.

Journal Articles

Unusually kinetically inert monocationic neptunyl complex with a fluorescein-modified 1,10-phenanthroline-2,9-dicarboxylate ligand; Specific separation and detection in gel electrophoresis

Yamagata, Kazuhito*; Ouchi, Kazuki; Marumo, Kazuki*; Tasaki-Handa, Yuiko*; Haraga, Tomoko; Saito, Shingo*

Inorganic Chemistry, 62(2), p.730 - 738, 2023/01

 Times Cited Count:2 Percentile:78.4(Chemistry, Inorganic & Nuclear)

The inert NpO$$_{2}$$$$^{+}$$ complex with a fluorescein-modified phenanthroline-2,9-dicarboxylic acid was found by kinetic selection using polyacrylamide gel electrophoresis (PAGE) from a small chemical library. The small spontaneous dissociation rate constant of 8$$times$$10$$^{-6}$$ s$$^{-1}$$ (the half-life of 23 hours) was determined. This is the singly-charged NpO$$_{2}$$$$^{+}$$ complex exhibiting unusual kinetic inertness in aqueous solution, one million times slower than widely accepted fast kinetics of neptunyl complexes. Selective fluorescence detection of NpO$$_{2}$$$$^{+}$$ was achieved in PAGE with a detection limit of 68 pmol dm$$^{-3}$$(17 fg). This system was successfully applied to simulated spent nuclear fuel and high-level radioactive waste samples.

Journal Articles

Application of high-energy-resolution X-ray absorption spectroscopy at the U L$$_{3}$$-edge to assess the U(V) electronic structure in FeUO$$_{4}$$

Yomogida, Takumi; Akiyama, Daisuke*; Ouchi, Kazuki; Kumagai, Yuta; Higashi, Kotaro*; Kitatsuji, Yoshihiro; Kirishima, Akira*; Kawamura, Naomi*; Takahashi, Yoshio*

Inorganic Chemistry, 61(50), p.20206 - 20210, 2022/12

 Times Cited Count:2 Percentile:36.89(Chemistry, Inorganic & Nuclear)

FeUO$$_{4}$$ was studied to clarify the electronic structure of U(V) in a metal monouranate compound. We obtained the peak splitting of HERFD-XANES spectra utilizing high-energy-resolution fluorescence detection-X-ray absorption near edge structure (HERFD-XANES) spectroscopy at the U L$$_{3}$$-edge, which is a novel technique in the U(V) compounds. Theoretical calculations revealed that the peak splitting was caused by splitting the 6d orbital of U(V). Such distinctive electronic states are of major interest to researchers and engineers working in various fields, from fundamental physics to the nuclear industry and environmental sciences for actinide elements.

Journal Articles

Magnetic and structure transition of Mn$$_{3-x}$$Fe$$_x$$O$$_4$$ solid solutions under high-pressure and high-temperature conditions

Yamanaka, Takamitsu*; Hirao, Naohisa*; Nakamoto, Yuki*; Mikouchi, Takashi*; Hattori, Takanori; Komatsu, Kazuki*; Mao, H.-K.*

Physics and Chemistry of Minerals, 49(10), p.41_1 - 41_14, 2022/10

 Times Cited Count:0 Percentile:0.02(Materials Science, Multidisciplinary)

Magnetic and crystal structure of Mn$$_{3-x}$$Fe$$_x$$O$$_4$$ solid solutions under high-PT conditions are investigated by neutron diffraction and synchrotron M${"o}$ssbauer spectroscopy. The ferrimagnetic-paramagnetic transition and tetragonal-cubic transition of Mn$$_2$$FeO$$_4$$ spinel occur at 100$$^circ$$C and 180$$^circ$$C, respectively, suggesting both the transitions are not coupled. The structure transition temperature decreases with pressure. M${"o}$ssbauer experiments and neutron diffraction revealed that the Fe$$^{2+}$$ occupancy in tetrahedral site increases increase with pressure, suggesting Mn$$_2$$FeO$$_4$$ phase approaches inverse spinel. Magnetic structure refinement clarified paramagnetic and ferrimagnetic structure of MnFe$$_2$$O$$_4$$ and Mn$$_2$$FeO$$_4$$. These spinels transform into high-pressure orthorhombic phases at 18.4 and 14.0 GPa, respectively, indicating lower transition pressure with increasing Mn content.

Journal Articles

Analysis of particles containing alpha-emitters in stagnant water at torus room of Fukushima Dai-ichi Nuclear Power Station's Unit 2 reactor

Yomogida, Takumi; Ouchi, Kazuki; Oka, Toshitaka; Kitatsuji, Yoshihiro; Koma, Yoshikazu; Konno, Katsuhiro*

Scientific Reports (Internet), 12(1), p.7191_1 - 7191_10, 2022/05

 Times Cited Count:4 Percentile:53.82(Multidisciplinary Sciences)

Particles containing alpha ($$alpha$$) nuclides were identified from sediment in stagnant water at the torus room of the Fukushima Dai-ichi Nuclear Power Station (FDiNPS)'s Unit 2 reactor. Several uranium-bearing particles were identified by SEM observation. These particles contained Zr and other elements which constituted fuel cladding and structural materials. The $$^{235}$$U/$$^{238}$$U isotope ratio in the solid fractions that included U particles was consistent with the nuclear fuel in the Unit 2 reactor, which indicated that the U particles had been derived from nuclear fuel. The particles with alpha-emitters detected by alpha track analysis were several tens to several hundred $$mu$$m in size. The EDX spectra showed that these particles mainly comprised iron, which indicated Pu, Am, and Cm were adsorbed on the Fe-baring particles. This study clarifies that the major morphologies of U and other $$alpha$$-nuclides were differed in the sediment of stagnant water in the torus room of FDiNPS's Unit 2 reactor.

Journal Articles

Design of microchannel suitable for packing with anion exchange resins; Uranium separation from seawater containing a large amount of cesium

Ouchi, Kazuki; Tsukahara, Takehiko*; Brandt, A.*; Muto, Yuki*; Nabatame, Nozomi*; Kitatsuji, Yoshihiro

Analytical Sciences, 37(12), p.1789 - 1794, 2021/12

 Times Cited Count:1 Percentile:6.71(Chemistry, Analytical)

We attempted to scale down a separation process of uranium (U) using the microchip column loaded with anion exchange resin to develop safety and waste-reducing separation technique. The ideal separation performance of U was obtained by the properly design of a microchannel. The concentration of U in seawater as a real-world sample could be quantified with the prepared microchip column. It indicates that the microchip column is sufficiently practical. Compared to separation of U with a general column, the column size was successfully scaled down to $$<$$ 1/5000.

Journal Articles

Electrochemical studies of uranium (IV) in an ionic liquid-DMF mixture to build a redox flow battery using uranium as an electrode active material

Ouchi, Kazuki; Komatsu, Atsushi; Takao, Koichiro*; Kitatsuji, Yoshihiro; Watanabe, Masayuki

Chemistry Letters, 50(6), p.1169 - 1172, 2021/06

 Times Cited Count:1 Percentile:6.77(Chemistry, Multidisciplinary)

The electrochemical behavior of uranium (IV) tetrachloride in ionic liquid-DMF mixture was studied for first time in order to build a redox flow battery (RFB) using U as an electrode active material. We found a quasi-reversible U$$^{III}$$/U$$^{IV}$$ couple that could be applied to the anode reaction of the RFB.

Journal Articles

Safe and rapid development of capillary electrophoresis for ultratrace uranyl ions in radioactive samples by way of fluorescent probe selection for actinide ions from a chemical library

Haraga, Tomoko; Ouchi, Kazuki; Sato, Yoshiyuki; Hoshino, Hitoshi*; Tanana, Rei*; Fujihara, Takashi*; Kurokawa, Hideki*; Shibukawa, Masami*; Ishimori, Kenichiro; Kameo, Yutaka; et al.

Analytica Chimica Acta, 1032, p.188 - 196, 2018/11

 Times Cited Count:12 Percentile:45.99(Chemistry, Analytical)

The development of safe, rapid and highly sensitive analytical methods for radioactive samples, especially actinide (An) ions, represents an important challenge. Here we propose a methodology for selecting appropriate emissive probes for An ions with very low consumption and emission of radioactivity by capillary electrophoresis-laser-induced fluorescence detection (CE-LIF), using a small chemical library of probes with eight different chelating moieties. It was found that the emissive probe, which possesses the tetradentate chelating moiety, was suitable for detecting uranyl ions. The detection limit for the uranyl-probe complex using CE-LIF combined with dynamic ternary complexation and on-capillary concentration techniques was determined to be 0.7 ppt. This method was successfully applied to real radioactive liquid samples collected from nuclear facilities.

Journal Articles

Deposition of uranium oxide following the reduction in weak acid solution using Electrochemical Quartz Crystal Microbalance (EQCM)

Ouchi, Kazuki; Otobe, Haruyoshi; Kitatsuji, Yoshihiro; Yamamoto, Masahiro

ECS Transactions, 75(27), p.51 - 57, 2017/01

 Times Cited Count:1 Percentile:38.46(Electrochemistry)

We investigated the deposition of U(IV) following a valence change of U as electrodeposition using an electrochemical quartz crystal microbalance (EQCM). When measurements of the reduction of U(VI) in a weak acid solution were performed, deposits of U(IV) were observed on the electrode surface. From deposition rates, pH dependence of them, and oxidation potentials of deposits, we proposed the following deposition mechanism. The deposition is divided into the three phases; First, in the induction phase, U(IV) produced by the disproportionation forms U(IV) hydroxide nucleus. Next, in the growth phase, U(IV) deposits begin to grow. In this phase, the deposits catalyze the reduction of U(V) to U(IV), resulting an increase of the reduction current. Finally, in the transformation phase, U(IV) hydroxide species transform into U dioxide having more stable state.

Journal Articles

XUV-FEL spectroscopy; He two-photon ionization cross-sections

Sato, Takahiro*; Iwasaki, Atsushi*; Ishibashi, Kazuki*; Okino, Tomoya*; Yamanouchi, Kaoru*; Adachi, Junichi*; Yagishita, Akira*; Yazawa, Hiroki*; Kannari, Fumihiko*; Aoyama, Makoto; et al.

Europhysics News, 42(5), P. 10, 2011/09

The resonant and non-resonant two-photon single ionization processes of He were investigated using intense free electron laser light in the extreme ultraviolet (XUV) region (53.4-61.4 nm) covering the 1s-2p and 1s-3p resonant transitions of He. On the basis of the dependences of the yield of He$$^{+}$$ on the XUV light-field intensity at 53.4, 58.4, 56.0 and 61.4 nm, the absolute values of the two-photon ionization cross sections of He at the four different wavelengths and their dependence on the light-field intensity were determined for the first time.

Journal Articles

Determination of the absolute two-photon ionization cross section of He by an XUV free electron laser

Sato, Takahiro*; Iwasaki, Atsushi*; Ishibashi, Kazuki*; Okino, Tomoya*; Yamanouchi, Kaoru*; Adachi, Junichi*; Yagishita, Akira*; Yazawa, Hiroki*; Kannari, Fumihiko*; Aoyama, Makoto; et al.

Journal of Physics B; Atomic, Molecular and Optical Physics, 44(16), p.161001_1 - 161001_5, 2011/08

 Times Cited Count:36 Percentile:82.78(Optics)

The resonant and non-resonant two-photon single ionization processes of He were investigated using intense free electron laser light in the extreme ultraviolet (XUV) region (53.4-61.4 nm) covering the 1s-2p and 1s-3p resonant transitions of He. On the basis of the dependences of the yield of He$$^{+}$$ on the XUV light-field intensity at 53.4, 58.4, 56.0 and 61.4 nm, the absolute values of the two-photon ionization cross sections of He at the four different wavelengths and their dependence on the light-field intensity were determined for the first time.

Oral presentation

Diffusion behavior of humic acid in compacted bentonite, 3; Diffusion mechanism of humic acid and neodymium

Iijima, Kazuki; Kurosawa, Seiichi*; Tobita, Minoru*; Kibe, Satoshi*; Ouchi, Yuji*

no journal, , 

Diffusion behavior of humic acid in compacted bentonite was investigated by through-diffusion method. Concentration profile and molecular weight distribution of humic acid in the compacted bentonite indicate that only low molecular weight fraction of humic acid is likely to diffuses. Difference of diffusion behavior arising from difference of molecular weight is considered to be taken into account in evaluation of diffusion parameters.

Oral presentation

Modelling of diffusion behaviour of humic acid and Nd in the presence of humic acid in compacted bentonite

Iijima, Kazuki; Kurosawa, Seiichi*; Kibe, Satoshi*; Tobita, Minoru*; Ouchi, Yuji*

no journal, , 

Diffusion behavior of humic acid and Nd in the presence of humic acid was investigated and modeled. Breakthrough of humic acid is observed in 0.1 and 1M NaCl with 1.2-1.6 Mg/m$$^{3}$$ dry density of compacted bentonite. The presence of humic acid facilitates the migration of Nd. Diffusion Parameters were evaluated from experimental results using the one dimensional diffusion model in which migration of several Nd species with different diffusion behaviors keeping equilibrium in parallel was taken into account. Obtained diffusion parameters for humic acid and Nd will be used for prediction of diffusion behavior of radionuclides in the presence of humic acid under various conditions.

Oral presentation

Development of the novel fluorescent probe for analysis of actinide by capillary electrophoresis-laser-induced fluorescence detection

Sato, Yoshiyuki; Haraga, Tomoko; Nakano, Yuta*; Ouchi, Kazuki; Ito, Yuki*; Ishimori, Kenichiro; Takahashi, Kuniaki; Saito, Shingo*

no journal, , 

For the development of a simple and rapid analytical method for actinides (Thorium, Uranium, Neptunium, Plutonium, Americium and Curium) in radioactive wastes, capillary electrophoresis-laser -induced fluorescence detecting method (CE-LIF) was studied. In this research, newly synthesized eight probes whose chelating group were acyclic or macrocyclic were applied to the detection of actinides using CE-LIF. As a result, Thorium and Uranium were successfully detected and separated from other actinide ions applied to octadenate acyclic probe and tetradenate planer probe, respectively. Neptunium was detected using hexadenate or heptadenate probes whose chelating groups were acyclic or macrocyclic. Plutonium was detected applied to hexadenate or octadenate acyclic probes. Americium and Curium were detected applied to seven probes except for tetradenate planer probe.

Oral presentation

Capillary electrophoresis with laser-induced fluorescence detection for ultratrace uranyl ion using a highly emissive phenanthroline-dicarboxylate derivative probe

Haraga, Tomoko; Sato, Yoshiyuki; Ouchi, Kazuki*; Shibukawa, Masami*; Ishimori, Kenichiro; Kameo, Yutaka; Saito, Shingo*

no journal, , 

Uranium is an important nuclide for the analysis of radioactive wastes from nuclear fuel cycle facilities. In order to achieve simple and rapid analysis of uranium, capillary electrophoresis-laser-induced fluorescent detection method (CE-LIF) is one of the potential candidates. In this study, a highly emissive probe of uranyl ion suitable for CE-LIF was developed. The detection and separation of uranyl ion were examined using several new emissive complexing probes, each of which possessed a fluorophore and a different chelating moiety. Using a tetradentate probe, phenanthroline dicarboxylic acid chelating moiety, the highly sensitive fluorescent detection of uranium was successfully achieved. The detection limit of mid-ppt levels was determined, and coexisting matrix metal ions, such as Ca$$^{2+}$$, Co$$^{2+}$$, Cs$$^{+}$$, Sr$$^{2+}$$, lanthanide ions and others, do not disturb the detection of uranium. This method has a great potential to be applied to analysis of radioactive waste samples.

Oral presentation

Safe and rapid analytical methods for actinide ions and radioactive Sr-90 in high-dose radiation samples using fluorescent probes in capillary electrophoresis

Haraga, Tomoko; Nakano, Yuta*; Sato, Yoshiyuki; Ouchi, Kazuki*; Hirose, Kazuki*; Shibukawa, Masami*; Ishimori, Kenichiro; Kameo, Yutaka; Saito, Shingo*

no journal, , 

no abstracts in English

Oral presentation

Electrode reaction of Np in a weakly acidic solution

Kitatsuji, Yoshihiro; Ouchi, Kazuki; Otobe, Haruyoshi

no journal, , 

Electrolytic reactions of Neptunium ions in a weakly acid solution were investigated by using gold electrode. It was reported previously that electrolytic reduction of Neptunium (V) ion based on mediator reaction with Np(III)/Np(IV) couple was observed in the acidic solution when bulk electrolysis was carried out at the potential around -0.2 V versus Ag/AgCl reference electrode. The reduction of Np(V), however, was not observed at the pH higher than 2. This is attributable to low reaction rate of electron exchange reaction between Np(V) and Np(III). Electrode reaction of Np(V) at more negative potential was investigated by cyclic voltammetry. The current peak due to reduction of Np(V) was observed at ca. -0.75 V, and oxidation current was appeared at +0.5 V. The reactions was determined to be reduction of Np(V) and oxidation of deposited species of reduction product of Np on the electrode. It was found that stripping current due to oxidation of deposit was saturated in spite of longer preelectrolysis time. This phenomenon is different from uranium.

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