Refine your search:     
Report No.
Search Results: Records 1-20 displayed on this page of 140

Presentation/Publication Type

Initialising ...


Journal/Book Title

Initialising ...

Meeting title

Initialising ...

First Author

Initialising ...


Initialising ...


Initialising ...

Publication Year

Initialising ...

Held year of conference

Initialising ...

Save select records

Journal Articles

Numerical simulation method using a Cartesian grid for oxidation of core materials under steam-starved conditions

Yamashita, Susumu; Sato, Takumi; Nagae, Yuji; Kurata, Masaki; Yoshida, Hiroyuki

Journal of Nuclear Science and Technology, 60(9), p.1029 - 1045, 2023/09

 Times Cited Count:0 Percentile:0.02(Nuclear Science & Technology)

Journal Articles

High-sensitive XANES analysis at Ce L$$_{2}$$-edge for Ce in bauxites using transition-edge sensors; Implications for Ti-rich geological samples

Li, W.*; Yamada, Shinya*; Hashimoto, Tadashi; Okumura, Takuma*; Hayakawa, Ryota*; Nitta, Kiyofumi*; Sekizawa, Oki*; Suga, Hiroki*; Uruga, Tomoya*; Ichinohe, Yuto*; et al.

Analytica Chimica Acta, 1240, p.340755_1 - 340755_9, 2023/02

 Times Cited Count:1 Percentile:42.63(Chemistry, Analytical)

no abstracts in English

Journal Articles

Stable C and N isotope abundances in water-extractable organic matter from air-dried soils as potential indices of microbially utilized organic matter

Nagano, Hirohiko*; Atarashi-Andoh, Mariko; Tanaka, Sota*; Yomogida, Takumi; Kozai, Naofumi; Koarashi, Jun

Frontiers in Forests and Global Change (Internet), 6, p.1228053_1 - 1228053_9, 2023/00

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:1 Percentile:27.23(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

Variation of crystallinity and secondary ion quantity of uranium particles with heating temperature of Sample preparation

Tomita, Ryohei; Tomita, Jumpei; Yomogida, Takumi; Suzuki, Daisuke; Yasuda, Kenichiro; Esaka, Fumitaka; Miyamoto, Yutaka

KEK Proceedings 2022-2, p.108 - 113, 2022/11

Automated Particle Measurement (APM) is the first measurement of environmental sample for safeguard purpose. APM tells us the number of particles in sample, their enrichment and their location. Precision and accuracy of APM is easily affected by particle condition. We have investigated how influential baking temperature in sample preparation are for uranium secondary ion quantity, uranium hydride generation and particle crystallinity. Our experimental results showed that baking temperature of 800$$^{circ}$$C reduced uranium secondary ion quantity to 33% compared with baking at 350$$^{circ}$$C. Uranium hydride generation ratio of the sample baked at 850$$^{circ}$$C was also 4 times higher than the sample baked at 350$$^{circ}$$C. Baking at 850$$^{circ}$$C raised only crystallinity of uranium particles. Baking sample at too high temperature caused less uranium secondary ion generation and much more uranium hydride generation. It made precision and accuracy of APM worse. In our experiment, baking at 350$$^{circ}$$C is suitable for uranium particles in the safeguards sample.

Journal Articles

Chemical state analysis of uranium dioxide particles by micro-Raman mapping

Yomogida, Takumi; Kitatsuji, Yoshihiro; Miyamoto, Yutaka

KEK Proceedings 2022-2, p.148 - 153, 2022/11

The Research Group for Safeguards Analytical Chemistry is currently developing a method to analyze the chemical state of uranium particles in environmental samples collected at nuclear facilities using micro-Raman spectroscopy. The chemical state of uranium particles in environmental samples can be partially oxidized by long-term exposure to air. It is necessary to develop a method to analyze the chemical state of the entire particle. In this study, uranium dioxide stored under atmospheric conditions was analyzed by micro-Raman mapping. The Raman spectra showed that uranium peroxide was locally present in the UO$$_{2}$$ particle. The Raman peaks originating from the structure of UO$$_{2}$$ around 570 cm$$^{-1}$$ and 1150 cm$$^{-1}$$ could not be observed in the point analysis of the particle center. On the other hand, in mapping analysis, Raman peaks originating from the structure of UO$$_{2}$$ can be observed from the same particle, demonstrating that Raman mapping analysis is an effective method for analyzing the chemical state of the entire particle.

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:3 Percentile:65.28(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

Dispersive XAFS Study on the Laser-Induced Reduction of a Rh$$^{3+}$$ ion complex; Presence of a Rh$$^{+}$$ Intermediate in Direct Photoreduction

Saeki, Morihisa*; Matsumura, Daiju; Nakanishi, Ryuzo*; Yomogida, Takumi; Tsuji, Takuya; Saito, Hiroyuki*; Oba, Hironori*

Journal of Physical Chemistry C, 126(12), p.5607 - 5616, 2022/03

 Times Cited Count:1 Percentile:21.52(Chemistry, Physical)

The reaction mechanism of the direct photoreduction of a Rh$$^{3+}$$ ion complex to a Rh$$^{0}$$ species induced by pulsed ultraviolet laser irradiation was studied using dispersive X-ray absorption fine structure (DXAFS) spectroscopy. The time-resolved X-ray absorption near edge structure (XANES) showed the absence of isosbestic points and suggested that more than two Rh$$^{n+}$$ species contribute toward the direct photoreduction of Rh$$^{3+}$$. Analysis of the time-resolved XANES data by singular value deposition showed that the direct photoreduction involves three Rh$$^{n+}$$ species. Multivariate curve resolution by alternating least-squares analysis (MCR-ALS) of the time-resolved XANES data gave pure spectra and concentration profiles of the three Rh$$^{n+}$$ species. The Rh$$^{n+}$$ species were assigned to Rh$$^{3+}$$, Rh$$^{+}$$, and Rh$$^{0}$$ species based on the features of the pure XANES spectra. The concentration profiles suggested that the direct photoreduction proceeds in the order of Rh$$^{3+}$$ $$rightarrow$$ Rh$$^{+}$$ $$rightarrow$$ Rh$$^{0}$$. A reaction mechanism, which was proposed involving photoreductions of Rh$$^{3+}$$ and Rh$$^{+}$$, photoinduced autocatalytic reductions of Rh$$^{3+}$$ and Rh$$^{+}$$, and photooxidation of Rh$$^{+}$$, well reproduced the concentration profiles of three Rh$$^{n+}$$ species.

Journal Articles

Selective Pd separation from simulated radioactive liquid waste by precipitation using xenon lamp irradiation for a simplified procedure

Yomogida, Takumi; Saeki, Morihisa*; Morii, Shiori; Oba, Hironori*; Kitatsuji, Yoshihiro

Analytical Sciences, 37(12), p.1843 - 1846, 2021/12

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

In this study, we developed a simple and one-step Pd separation technique based on photoreduction with Xe lamp irradiation for the determination of $$^{107}$$Pd in highly radioactive samples. A simulated high-level radioactive liquid wastes (HLLW) solution, which consists of 14 major elements (Rb, Sr, Zr, Mo, Ru, Rh, Pd, Cs, Ba, La, Ce, Pr, Nd, Sm) in a 3 mol L$$^{-1}$$ HNO$$_{3}$$ solution, was used to evaluate the separation performance. The Pd precipitate were formed by Xe lamp irradiation and recovered by centrifugation. The results showed that the recovery of Pd from a simulated HLLW solution depend on the irradiation time and concentration of ethanol. By optimizing the conditions at photo irradiation, the Pd recovery from the simulated HLLW solution reached up to 50 %, while 99.5 % of the other 13 elements were separated. The Pd precipitate could be separated from the elements that are the main source of radioactivity (Sr, Cs, and Ba) and the source of spectral interference for the determination of $$^{107}$$Pd (Zr, and Ru). These results indicate that selective separation of Pd is achieved with the proposed method, showing the applicability of the proposed separation technique to HLLW samples.

Journal Articles

Optimization of SIMS-APM for high enrichment uranium particles including higher uranium hydride

Tomita, Ryohei; Tomita, Jumpei; Yomogida, Takumi; Suzuki, Daisuke; Yasuda, Kenichiro; Esaka, Fumitaka; Miyamoto, Yutaka

KEK Proceedings 2021-2, p.146 - 150, 2021/12

no abstracts in English

Journal Articles

Distribution of studtite and metastudtite generated on the surface of U$$_{3}$$O$$_{8}$$; Application of Raman imaging technique to uranium compound

Kusaka, Ryoji; Kumagai, Yuta; Yomogida, Takumi; Takano, Masahide; Watanabe, Masayuki; Sasaki, Takayuki*; Akiyama, Daisuke*; Sato, Nobuaki*; Kirishima, Akira*

Journal of Nuclear Science and Technology, 58(6), p.629 - 634, 2021/06

 Times Cited Count:7 Percentile:70.19(Nuclear Science & Technology)

Journal Articles

Characteristics of fault fracture zones of the activated Shionohira Fault and the non-activated Kuruma Fault of the 2011 Fukushima-ken Hamadori Earthquake, Northeast Japan

Aoki, Kazuhiro; Tanaka, Yukumo; Yoshida, Takumi; Shimada, Koji; Sakai, Toru*; Kametaka, Masao*; Seshimo, Kazuyoshi

Oyo Chishitsu, 62(2), p.64 - 81, 2021/06

Co-seismic surface ruptures in the Fukushima-ken Hamadori Earthquake of Mw 6.7 on April 11, 2011 exposed approximately 14 km trending NNW-SSE from Nameishi to northwest of Ishizumi Tsunaki of Tabito Town, Iwaki City and were newly named the Shionohira Fault. However, no surface ruptures appeared along an N-S trending active Kuruma fault extending 5 km south of the Shionohira Fault. Because of the proximity and similar strike, two locations in Shionohira Fault and one location in Kuruma fault were selected as the study area for the fault activity evaluation. The present study reports the results of a series of geological and drilling surveys, core observation, XRD, isotope, and fluid inclusion analyses, and water permeability test. The results obtained from the three locations offer a fundamental data base that can be utilized for fault activity evaluation by summarizing the geological, mineralogical, and fluid property characteristics of fault fracture zone.

Journal Articles

Radioactivity and radionuclides in deciduous teeth formed before the Fukushima-Daiichi Nuclear Power Plant accident

Takahashi, Atsushi*; Chiba, Mirei*; Tanahara, Akira*; Aida, Jun*; Shimizu, Yoshinaka*; Suzuki, Toshihiko*; Murakami, Shinobu*; Koarai, Kazuma; Ono, Takumi*; Oka, Toshitaka; et al.

Scientific Reports (Internet), 11(1), p.10355_1 - 10355_11, 2021/05

 Times Cited Count:5 Percentile:40.82(Multidisciplinary Sciences)

Journal Articles

Observation of dihydrogen bonds in high-pressure phases of ammonia borane by X-ray and neutron diffraction measurements

Nakano, Satoshi*; Sano, Asami; Hattori, Takanori; Machida, Shinichi*; Komatsu, Kazuki*; Fujihisa, Hiroshi*; Yamawaki, Hiroshi*; Goto, Yoshito*; Kikegawa, Takumi*

Inorganic Chemistry, 60(5), p.3065 - 3073, 2021/03

 Times Cited Count:8 Percentile:74.88(Chemistry, Inorganic & Nuclear)

X-ray and neutron diffraction analyses of ammonia borane were conducted at ambient and high pressures. The H-H distance in dihydrogen bonds was shorter than twice the van der Waals radius (2.4 ${AA}$). The half of the dihydrogen bonds were broken on phase transition from AP to the first high pressure phase (HP1) at approximately 1.2 GPa as revealed by an increase in the H-H distances. On further pressure increase, all of the H-H distances became shorter than 2.4 ${AA}$ again, implying the pressure-induced reformation of the dihydrogen bonds. Furthermore, the HP1 transformed to the second one with the structure of $$P2_1$$ (Z = 2) at about 11 GPa. In this phase transition, the inclination of the molecule axis became larger and the number of types of dihydrogen bonds increased from 6 to 11. Just before the third transition at 18.9 GPa, the shortest dihydrogen bond decreased to 1.65 ${AA}$. The present study experimentally first confirmed the breakage and reformation of the dihydrogen bonds by the structural change under pressure.

Journal Articles

Morphological reproductive characteristics of testes and fertilization capacity of cryopreserved sperm after the Fukushima accident in raccoon (${it Procyon lotor}$)

Komatsu, Kazuki*; Iwasaki, Tsugumi*; Murata, Kosuke*; Yamashiro, Hideaki*; Goh, V. S. T.*; Nakayama, Ryo*; Fujishima, Yohei*; Ono, Takumi*; Kino, Yasushi*; Shimizu, Yoshinaka*; et al.

Reproduction in Domestic Animals, 56(3), p.484 - 497, 2021/03

 Times Cited Count:9 Percentile:90.55(Agriculture, Dairy & Animal Science)

We have established an archive system of livestock and wild animals from the surrounding ex-evacuation zone. Wildlife within the alert zone have been exposed to low-dose-rate (LDR) radiation for a long and continuous time. In this study, we analysed the morphological characteristics of the testes and in vitro fertilization (IVF) capacity of cryopreserved sperm of raccoons from the ex-evacuation zone of the FDNPP accident. This study revealed that the chronic and LDR radiation exposure associated with the FDNPP accident had no adverse effect on the reproductive characteristics and functions of male raccoons.

Journal Articles

Application of an augmentation method to MCR-ALS analysis for XAFS and Raman data matrices in the structural change of isopolymolybdates

Saeki, Morihisa*; Yomogida, Takumi; Matsumura, Daiju; Saito, Takumi*; Nakanishi, Ryuzo*; Tsuji, Takuya; Oba, Hironori*

Analytical Sciences, 36(11), p.1371 - 1378, 2020/11

 Times Cited Count:2 Percentile:11.27(Chemistry, Analytical)

We measured X-ray absorption fine structure (XAFS) and Raman spectra of isopolymolybdates(VI) in HNO$$_{3}$$ solution (0.15- 4.0 M), which change their geometries depending on acid concentration, and performed simultaneous resolution of the XAFS and Raman data using a multivariate curve resolution by alternating least-squares (MCR-ALS) analysis. In iterative ALS optimization, initial data matrices were prepared by two different methods. The MCR-ALS result of single XAFS data matrix shows large dependence on the preparation method of the initial data matrices. The MCR-ALS result of an augmented matrix of Raman and XAFS data has little dependence on the initial data matrices. It indicates that the augmentation method effectively improves the rotation ambiguities in the MCR-ALS analysis of the XAFS data. Based on the model fitting of the pure EXAFS oscillations, we revealed the change of [Mo$$_{36}$$O$$_{112}$$(H$$_{2}$$O)$$_{16}$$]$$^{2+}$$ $$rightarrow $$ [Mo$$_{2}$$O$$_{5}$$(H$$_{2}$$O)$$_{6}$$]$$^{2+}$$ $$rightarrow $$ [HMoO$$_{3}$$(H$$_{2}$$O)$$_{3}$$]$$^{+}$$ in the highly concentrated HNO$$_{3}$$ solution.

Journal Articles

Observation of a $$bar{K}NN$$ bound state in the $$^{3}$$He $$(K^-, Lambda p)n$$ reaction

Yamaga, Takumi*; Hashimoto, Tadashi; Tanida, Kiyoshi; 66 of others*

Physical Review C, 102(4), p.044002_1 - 044002_14, 2020/10

 Times Cited Count:13 Percentile:86.16(Physics, Nuclear)

Journal Articles

Direct quantitation of $$^{135}$$Cs in spent Cs adsorbent used for the decontamination of radiocesium-containing water by laser ablation inductively coupled plasma mass spectrometry

Asai, Shiho*; Ohata, Masaki*; Hanzawa, Yukiko; Horita, Takuma; Yomogida, Takumi; Kitatsuji, Yoshihiro

Analytical Chemistry, 92(4), p.3276 - 3284, 2020/02

 Times Cited Count:4 Percentile:25.1(Chemistry, Analytical)

The long-term safety assessment of spent Cs adsorbents produced during the decontamination of radiocesium-containing water at the Fukushima Daiichi Nuclear Power Plant requires one to estimate their $$^{135}$$Cs content prior to final disposal. $$^{135}$$Cs is usually quantified by inductively coupled plasma mass spectrometry (ICP-MS), which necessitates the elution of Cs from Cs adsorbents. However, this approach suffers from the high radiation dose from $$^{137}$$Cs. To address this challenge, we herein employed laser ablation ICP-MS for direct quantitation of $$^{135}$$Cs in Cs adsorbents and used a model Cs adsorbent prepared by immersion of a commercially available Cs adsorbent into radiocesium-containing liquid waste to verify the developed technique. The use of the $$^{135}$$Cs/$$^{137}$$Cs ratio and $$^{137}$$Cs radioactivity obtained by gamma spectrometry achieved simple and precise quantitation of $$^{135}$$Cs and the resulting $$^{135}$$Cs activity of 0.36 Bq agreed well with that in the original radiocesium-containing liquid waste.

Journal Articles

Results of $$bar{K}NN$$ search via the $$(K^-, n)$$ reaction at J-PARC

Yamaga, Takumi*; Hashimoto, Tadashi; Tanida, Kiyoshi; 66 of others*

JPS Conference Proceedings (Internet), 26, p.023008_1 - 023008_6, 2019/11

Journal Articles

Determination of $$^{107}$$Pd in Pd purified by selective precipitation from spent nuclear fuel by laser ablation ICP-MS

Asai, Shiho; Ohata, Masaki*; Yomogida, Takumi; Saeki, Morihisa*; Oba, Hironori*; Hanzawa, Yukiko; Horita, Takuma; Kitatsuji, Yoshihiro

Analytical and Bioanalytical Chemistry, 411(5), p.973 - 983, 2019/02

 Times Cited Count:10 Percentile:59.18(Biochemical Research Methods)

Determination of radiopalladium $$^{107}$$Pd is required for ensuring the radiation safety of Pd extracted from spent nuclear fuel for recycling or disposal. We employed laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) to simplify an analytical procedure of $$^{107}$$Pd. Pd was separated through selective Pd precipitation reaction from spent nuclear fuel. Laser ablation allows direct measurement of the Pd precipitates, skipping the dissolution and dilution procedure. In this study, $$^{102}$$Pd in natural Pd standard solution was used as an internal standard, taking advantage of its absence in spent nuclear fuel. The Pd precipitate was uniformly embedded on the surface of the centrifugal filter, forming a microscopically thin flat surface of Pd. The resulting homogeneous Pd layer is suitable for obtaining a stable signal ratio of $$^{107}$$Pd/$$^{102}$$Pd. The amount of $$^{107}$$Pd obtained by LA-ICP-MS corresponds to the values obtained by conventional solution nebulization measurement.

140 (Records 1-20 displayed on this page)