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Journal Articles

Ordered graphane nanoribbons synthesized via high-pressure diels-alder polymerization of 2,2'-bipyrazine

Li, F.*; Tang, X.*; Fei, Y.*; Zhang, J.*; Liu, J.*; Lang, P.*; Che, G.*; Zhao, Z.*; Zheng, Y.*; Fang, Y.*; et al.

Journal of the American Chemical Society, 147(17), p.14054 - 14059, 2025/04

We synthe-sized a crystalline graphane nanoribbon (GANR) via pressure-in-duced polymerization of 2,2'-bipyrazine (BPZ). By performing Rietveld refinement of in situ neutron diffraction data, nuclear magnetic resonance spectroscopy, infrared spectra, and theoretical calculation, we found that BPZ experienced Diels-Alder polymeri-zation between the $$pi$$ $$cdots$$ $$pi$$ stacked aromatic rings, and formed extended boat-GANR structures with exceptional long-range order. The unreacted -C=N- groups bridge the two ends of the boat, and ready for further functionalization. The GANR has a bandgap of 2.25 eV, with booming photoelectric response (I$$_{on}$$/I$$_{off}$$ =18.8). Our work highlights that the high-pressure topochemical polymeriza-tion is a promising method for the precise synthesis of graphane with specific structure and desired properties.

JAEA Reports

Evaluation of exposure doses and reduction factor for sheltering for each nuclear site under each accident scenario (Contract research)

Hirouchi, Jun; Watanabe, Masatoshi*; Hayashi, Naho; Nagakubo, Azusa; Takahara, Shogo

JAEA-Research 2024-015, 114 Pages, 2025/03

JAEA-Research-2024-015.pdf:10.03MB

The public living in areas contaminated by nuclear accidents is exposed to radiation in the early phase and over the long term. Even under the same accident scenario, the exposure doses and the effectiveness of sheltering, which is one of the protective measures, vary depending on the meteorological condition and the surrounding environment. The exposure doses and sheltering effectiveness in the early phase are important information for the public and the national and local governments planning a nuclear emergency preparedness. In this report, we evaluate the exposure doses and sheltering effectiveness at sites with nuclear facilities in Japan using OSCAAR, one of the probabilistic risk assessment codes, for five accident scenarios: three scenarios from past severe accident studies; a scenario defined by the Nuclear Regulatory Authority; and a scenario assuming the Fukushima Daiichi Nuclear Power Station accident. The sheltering effectiveness differed by approximately 20% among the sites. This was due to the differences in wind speed among the sites.

Journal Articles

Quantitative evaluation of carbon dioxide emissions from the subsoils of volcanic and non-volcanic ash soils in temperate forest ecosystems

Abe, Yukiko; Nakayama, Masataka*; Atarashi-Andoh, Mariko; Tange, Takeshi*; Sawada, Haruo*; Liang, N.*; Koarashi, Jun

Geoderma, 455, p.117221_1 - 117221_11, 2025/03

 Times Cited Count:0 Percentile:0.00(Soil Science)

Subsoils (typically below a depth of 30 cm) contain more than half of global soil carbon (C) as soil organic C (SOC). However, the extent to which subsoil SOC contributes to the global C cycle and the factors that control it are unclear because quantitative evaluation of carbon dioxide (CO$$_{2}$$) emission from subsoils through direct observations is limited. This study aimed to quantify CO$$_{2}$$ emission from subsoils and determine factors that control CO$$_{2}$$ emission, focusing on the decomposability of soil organic matter (SOM) and the characteristics of the mineral-SOM association in soils. Therefore, a laboratory incubation experiment was conducted using surface soils (0-10 cm and 10-25 cm depth) and subsoils (30-45 cm and 45-60 cm depth) collected from four Japanese forest sites with two different soil types (volcanic ash and non-volcanic ash soils). The CO$$_{2}$$ emission from the subsoils was found to be responsible for 6%-23% of total CO$$_{2}$$ emission from the upper 60-cm mineral soil across all sites. Radiocarbon signatures of CO$$_{2}$$ released from the subsoils indicated the decomposition of decades-old SOM in the subsoils. The correlations between CO$$_{2}$$ emission rate and soil factors across both soil types suggested that the CO$$_{2}$$ emission from the subsoils is mainly controlled by the amounts of SOC easily available to soil microbes and microbial biomass C, not by the amounts of reactive minerals. Given the potential active participation of subsoils in terrestrial C cycling, most of the current soil C models that ignore subsoil C cycling are likely to underestimate the response of soil C to future climate change. The quantitative and mechanistic understanding of C cycling through a huge subsoil C pool is critical to accurately evaluating the role of soil C in the global C balance.

Journal Articles

Effects of different accident scenarios and sites on the reduction factor used for expressing sheltering effectiveness

Hirouchi, Jun; Watanabe, Masatoshi*; Hayashi, Naho; Nagakubo, Azusa; Takahara, Shogo

Journal of Radiological Protection, 45(1), p.011506_1 - 011506_11, 2025/03

 Times Cited Count:0 Percentile:0.00(Environmental Sciences)

Public living in areas contaminated by nuclear accidents is exposed to radiation in the early phase and over the long term. Even under similar accident scenarios, radiation doses and sheltering effectiveness, which is one of the protective measures, depend on meteorological conditions and the surrounding environment. Radiation doses and sheltering effectiveness in the early phase of nuclear accidents are crucial information for the public as well as national and local governments planning a nuclear emergency preparedness. In this study, we assessed radiation doses and sheltering effectiveness at sites with nuclear facilities in Japan using the Off-Site Consequence Analysis code for Atmospheric Release accidents, which is one of the level-3 probabilistic risk assessment codes, for five accident scenarios: three scenarios from past severe accident studies, a scenario defined by the Nuclear Regulation Authority in Japan, and a scenario corresponding to the Fukushima-Daiichi Nuclear Power Station accident. The sheltering effectiveness differed by up to approximately 50% among the accident scenarios at the same sites and by approximately 20%$$sim$$50% among sites under the same accident scenario. Differences in the radionuclide composition among the accident scenarios and the differences in wind speeds among the sites primarily caused these differences in sheltering effectiveness.

Journal Articles

Spontaneous magnetic field and disorder effects in BaPtAs$$_{1-x}$$Sb$$_x$$ with a honeycomb network

Adachi, Tadashi*; Ogawa, Taiki*; Komiyama, Yota*; Sumura, Takuya*; Saito-Tsuboi, Yuki*; Takeuchi, Takaaki*; Mano, Kohei*; Manabe, Kaoru*; Kawabata, Koki*; Imazu, Tsuyoshi*; et al.

Physical Review B, 111(10), p.L100508_1 - L100508_6, 2025/03

 Times Cited Count:0

Journal Articles

Achievements and status of the STRAD project for radioactive liquid waste management

Arai, Yoichi; Watanabe, So; Nakahara, Masaumi; Funakoshi, Tomomasa; Hoshino, Takanori; Takahatake, Yoko; Sakamoto, Atsushi; Aihara, Haruka; Hasegawa, Kenta; Yoshida, Toshiki; et al.

Progress in Nuclear Science and Technology (Internet), 7, p.168 - 174, 2025/03

The Japan Atomic Energy Agency (JAEA) has been conducting a project named "Systematic Treatment of RAdioactive liquid waste for Decommissioning (STRAD)" project since 2018 for fundamental and practical studies for treating radioactive liquid wastes with complicated compositions. Fundamental studies have been conducted using genuine liquid wastes accumulated in a hot laboratory of the JAEA called the Chemical Processing Facility (CPF), and treatment procedures for all liquid wastes in CPF were successfully designed on the results obtained. As the next phase of the project, new fundamental and practical studies on primarily organic liquid wastes accumulated in different facilities of JAEA are in progress. This paper reviews the representative achievements of the STRAD project and introduces an overview of ongoing studies.

JAEA Reports

Decommissioning report for Wastewater Treatment Facility (Part 2); Chapter on contamination inspection section

Yamamoto, Keisuke; Nakagawa, Takuya; Shimojo, Hiroto; Kijima, Jun; Miura, Daiya; Onose, Yoshihiko*; Namba, Koji*; Uchida, Hiroaki*; Sakamoto, Kazuhiko*; Ono, Chika*; et al.

JAEA-Technology 2024-019, 211 Pages, 2025/02

JAEA-Technology-2024-019.pdf:35.35MB

The uranium enrichment facilities at the Nuclear Fuel Cycle Engineering Laboratories of Japan Atomic Energy Agency (JAEA) were constructed sequentially to develop uranium enrichment technology with centrifugal separation method. The developed technologies were transferred to Japan Nuclear Fuel Limited until 2001. And the original purpose has been achieved. Wastewater Treatment Facility, one of the uranium enrichment facilities, was constructed in 1976 to treat radioactive liquid waste generated at the facilities, and it finished the role in 2008. In accordance with the Medium/Long-Term Management Plan of JAEA Facilities, interior equipment installed in this facility had been dismantled and removed since November 2021 to August 2023. This report summarizes the findings obtained through the work related to the contamination inspection methods cancellation the controlled area of Wastewater Treatment Facility from September 2023 to March 2024.

Journal Articles

Gyro-spintronic material science using vorticity gradient in solids

Nozaki, Yukio*; Sukegawa, Hiroaki*; Watanabe, Shinichi*; Yunoki, Seiji*; Horaguchi, Taisuke*; Nakayama, Hayato*; Yamanoi, Kazuto*; Wen, Z.*; He, C.*; Song, J.*; et al.

Science and Technology of Advanced Materials, 26(1), p.2428153_1 - 2428153_39, 2025/02

 Times Cited Count:0 Percentile:0.00(Materials Science, Multidisciplinary)

Journal Articles

High-pressure polymerization of phenol toward degree-4 carbon nanothread

Yang, X.*; Che, G.*; Wang, Y.*; Zhang, P.*; Tang, X.*; Lang, P.*; Gao, D.*; Wang, X.*; Wang, Y.*; Hattori, Takanori; et al.

Nano Letters, 25(3), p.1028 - 1035, 2025/01

 Times Cited Count:0 Percentile:0.00(Chemistry, Multidisciplinary)

Saturated sp$$^3$$-carbon nanothreads (CNTh) have garnered significant interest due to their predicted high Young's modulus and thermal conductivity. While the incorporation of heteroatoms into the central ring has been shown to influence the formation of CNTh and yield chemically homogeneous products, the impact of pendant groups on the polymerization process remains underexplored. In this study, we investigate the pressure-induced polymerization of phenol, revealing two phase transitions occurring below 0.5 and 4 GPa. Above 20 GPa, phenol polymerizes into degree-4 CNThs featuring hydroxyl and carbonyl groups. Hydrogen transfer of hydroxyl groups was found to hinder the formation of degree-6 nanothreads. Our findings highlight the crucial role of the hydroxyl group in halting further intracolumn polymerization and offer valuable insights for future mechanism research and nanomaterial synthesis.

Journal Articles

Pressure-induced polymerization of 1,4-difluorobenzene towards fluorinated diamond nanothreads

Che, G.*; Fei, Y.*; Tang, X.*; Zhao, Z.*; Hattori, Takanori; Abe, Jun*; Wang, X.*; Ju, J.*; Dong, X.*; Wang, Y.*; et al.

Physical Chemistry Chemical Physics, 27(2), p.1112 - 1118, 2025/01

 Times Cited Count:2 Percentile:47.21(Chemistry, Physical)

Pressure-induced polymerization (PIP) of aromatic molecules has emerged as an effective method for synthesizing various carbon-based materials. In this work, PIP of 1,4-difluorobenzene (1,4-DFB) was investigated. ${it In situ}$ high-pressure investigations of 1,4-DFB reveal a phase transition at approximately 12.0 GPa and an irreversible chemical reaction at 18.7 GPa. Structural analysis of the product and the kinetics of the reaction uncovered the formation of pseudohexagonal stacked fluoro-diamond nanothreads with linear growth. Compared to the crystal structures of benzene under high pressure, 1,4-DFB exhibits higher compression along the [001] axis. The anisotropic compression is attributed to the stronger H$$cdot cdot cdot pi$$ interaction along the [01$$overline{1}$$] axis and the potential compression-inhibiting H$$cdot cdot cdot$$F interactions along the [100] and [010] axes, and it facilitates a possible reaction pathway along the [01$$overline{1}$$] axis. This work emphasizes the crucial role of functionalization in modulating molecular stacking and influencing the reaction pathway.

Journal Articles

Solid-state Alder-ene reaction of 1-hexene under high pressure

Xu, J.*; Lang, P.*; Liang, S.*; Zhang, J.*; Fei, Y.*; Wang, Y.*; Gao, D.*; Hattori, Takanori; Abe, Jun*; Dong, X.*; et al.

Journal of Physical Chemistry Letters (Internet), p.2445 - 2451, 2025/00

 Times Cited Count:0 Percentile:0.00(Chemistry, Physical)

The Alder-ene reaction is a chemical reaction between an alkene with an allylic hydrogen, and it provides an efficient method to construct the C-C bond. Traditionally, this reaction requires catalysts, high temperatures, or photocatalysis. In this study, we reported a high-pressure-induced solid-state Alder-ene reaction of 1-hexene at room temperature without a catalyst. 1-Hexene crystallizes at 4.3 GPa and polymerizes at 18 GPa, forming olefins. By exploring gas chromatography-mass spectrometry, we discovered that 1-hexene generates dimeric products through the Alder-ene reaction under high pressures. The in situ neutron diffraction shows that the reaction process did not obey the topochemical rule. A six-membered ring transition state including one C-H $$sigma$$ bond and two alkene $$pi$$ bonds was evidenced by the theoretical calculation, whose energy obviously decreased when compressed to 20 GPa. Our work offers a novel and promising method to realize the Alder-ene reaction at room temperature without a catalyst, expanding the application of this important reaction.

Journal Articles

Performance study of a new LiCAF:Ce detector developed for high-efficient neutron detection in intense $$gamma$$-ray fields

Kaburagi, Masaaki; Kamada, Kei*; Ishii, Junya*; Matsumoto, Tetsuro*; Manabe, Seiya*; Masuda, Akihiko*; Harano, Hideki*; Kato, Masahiro*; Shimazoe, Kenji*

Journal of Instrumentation (Internet), 19(11), p.P11019_1 - P11019_16, 2024/11

 Times Cited Count:0 Percentile:0.00(Instruments & Instrumentation)

Journal Articles

Quantitative importance of subsoil nitrogen cycling processes in Andosols and Cambisols under temperate forests

Nakayama, Masataka; Abe, Yukiko; Atarashi-Andoh, Mariko; Tange, Takeshi*; Sawada, Haruo*; Liang, N.*; Koarashi, Jun

Applied Soil Ecology, 201, p.105485_1 - 105485_12, 2024/09

 Times Cited Count:2 Percentile:69.21(Soil Science)

Nitrogen often limits plant growth in forest ecosystems. Plants, including trees, change vertical root distribution when nutrient competition is strong within surface soil layer and take up nitrogen even from subsurface soil layers in addition to the surface soil. However, there is still limited knowledge about nitrogen cycles within deeper soil layers. In this study, we investigated the vertical profiles (0-60 cm) of the net nitrogen mineralization and nitrification rates at four Japanese forest sites with two different soil types (Andosols and Cambisols). The partial least square path modeling (PLS-PM) was used to determine factors affecting nitrogen-cycling processes. The net nitrogen mineralization and nitrification rates per unit soil weight were considerably higher in surface soil layer than in deeper soil layers in Andosols but not in Cambisols. PLS-PM analysis showed that microbial biomass and soil organic matter quantities were the main factors influencing the net nitrogen mineralization and nitrification rates, indicating that a similar mechanism creating the spatial variations of nitrogen-cycling processes in surface soil layer predominantly regulates the processes in subsoil layers. Moreover, it was estimated that the net nitrogen mineralization rate could be comparable at all soil types and depths when the rate was expressed per unit soil volume. Therefore, our results suggest that subsoil layers are a quantitatively important nitrogen source for plant nutrients in Andosols and Cambisols, supporting high forest productivity.

Journal Articles

Cavity ionization chamber responses in the JAEA and the NMIJ high-energy photon reference fields for radiation protection

Ishii, Junya*; Shimizu, Morihito*; Kato, Masahiro*; Kurosawa, Tadahiro*; Tsuji, Tomoya; Yoshitomi, Hiroshi; Tanimura, Yoshihiko; Watabe, Hiroshi*

Journal of Radiological Protection, 44(3), p.031516_1 - 031516_8, 2024/09

 Times Cited Count:0 Percentile:0.00(Environmental Sciences)

Journal Articles

Development of a diamond anvil cell for high-pressure neutron diffraction experiments

Machida, Shinichi*; Hattori, Takanori; Nakano, Satoshi*; Sano, Asami; Funakoshi, Kenichi*; Abe, Jun*

Koatsuryoku No Kagaku To Gijutsu, 34(3), p.134 - 142, 2024/09

A diamond anvil cell (DAC) for high-pressure neutron diffraction experiments has been developed at the PLANET beamline, Materials and Life Science Experimental Facility, in J-PARC. The conically supported diamond anvils were used for high-pressure generation. We succeeded in obtaining the neutron data for D$$_2$$O ice up to 69.4 GPa. In addition, the gasket materials suitable for the neutron diffraction measurements were investigated. 11 kinds of alloys were tested and SUS304, Inconel718 and M2052 (73Mn-20Cu-5Ni-2Fe, at%) alloys showed excellent performance. Especially, M2052 null-matrix alloy has proven to be useful for neutron diffraction experiments where the beam inevitably hits the gasket. We then obtained refinable neutron diffraction profiles in Rietveld analysis from D$$_2$$O ice at least up to 43.3 GPa.

Journal Articles

Hydroxyl group/fluorine disorder in deuterated magnesium hydroxyfluoride and behaviors of hydrogen bonds under high pressure

He, X.*; Kagi, Hiroyuki*; Komatsu, Kazuki*; Iizuka, Riko*; Okajima, Hajime*; Hattori, Takanori; Sano, Asami; Machida, Shinichi*; Abe, Jun*; Goto, Hirotada*; et al.

Journal of Molecular Structure, 1310, p.138271_1 - 138271_8, 2024/08

 Times Cited Count:0 Percentile:0.00(Chemistry, Physical)

High-pressure responses of the O-D$$cdotcdotcdot$$F hydrogen bonds in deuterated magnesium hydroxyfluoride were investigated using neutron powder diffraction and Raman spectroscopy. The Rietveld analysis at ambient conditions revealed a chemical formula of Mg(OD)$$_{0.920(12)}$$F$$_{1.080(12)}$$ and hydroxyl group/fluorine disorder (OD/F disorder) in the crystal structure, which gave rise to two hydrogen-bonding configurations. The Rietveld analysis showed the hydrogen-bonding geometries remains up to 9.8 GPa, indicating no pressure-induced strengthening of hydrogen bonds. The Raman spectra at ambient conditions showed three hydroxyl stretching bands at 2613, 2694, and 2718 cm$$^{-1}$$. The high frequencies of the O-D stretching modes indicated that the hydroxyls should be involved in weak or none hydrogen-bonding interactions. Up to 20.2 GPa, the mode initially centered at 2694 cm$$^{-1}$$ displayed a pressure-induced blue shift, revealing no strengthening of hydrogen bonds under compression. We discuss the existence of hydrogen bonds and the causes of the blue-shifting hydroxyls at ambient and at high pressures.

Journal Articles

Present and new operational quantities evaluated from photon spectrum measurements at workplaces in the research reactor and accelerator facility at the JAEA

Tanimura, Yoshihiko; Yoshitomi, Hiroshi; Nishino, Sho; Tsuji, Tomoya; Fukami, Tomoyo; Shinozuka, Tomoki; Oishi, Kohei; Ishii, Masato; Takamiya, Kei; Onuki, Takaya; et al.

Radiation Measurements, 176, p.107196_1 - 107196_6, 2024/08

 Times Cited Count:1 Percentile:0.00(Nuclear Science & Technology)

The ICRU has proposed to change the definitions of the operational quantities used for the area and individual monitoring for external exposure in the ICRU Report 95. As introducing the new operational quantities into the radiation monitoring may affect the dose assessment results using the present personal dosimeters, it is necessary to characterize the energy spectrum in the workplace and the energy dependency of the dosimeters to be used. In this work the photon spectra were measured using a NaI(Tl) scintillation detector or a LaBr$$_3$$(Ce) scintillation detector at the workplaces in the Japanese Research Reactor No.3 (JRR-3) and the Japan Proton Accelerator Research Complex (J-PARC) at Japan Atomic Energy Agency (JAEA). Then the present and new operational quantities were evaluated using the above mention spectra at the workplaces and compared each other.

Journal Articles

SRPES and XPS analysis of activation and deterioration processes for Ti-Zr-V NEG coating

Kamiya, Junichiro; Abe, Kazuhide; Fujimori, Shinichi; Fukuda, Tatsuo; Kobata, Masaaki; Morohashi, Yuko; Tsuda, Yasutaka; Yamada, Ippei; Yoshigoe, Akitaka

e-Journal of Surface Science and Nanotechnology (Internet), 22(4), p.316 - 326, 2024/08

The activation and deterioration mechanisms of the Ti-Zr-V non-evaporable getter (NEG) coating have been investigated. Operando analysis of the surface chemical composition change of the Ti-Zr-V coating was performed by the synchrotron radiation photoelectron spectroscopy (SRPES) during the process of raising the sample temperature to 250$$^{circ}$$C, corresponding to the activation process of NEG coating. The surface oxidation process was also characterized by the SRPES during the injection of O_2 gas into the chamber while keeping the sample temperature at 250$$^{circ}$$C, corresponding to the deterioration process of NEG coating, i.e. surface oxidation and oxygen diffusion to the coating interior. The depth profile of the oxidized sample was measured with X-ray photoelectron spectroscopy. The results shows, in the activation process, the surface Zr gets the oxygen from the oxides of Ti and V at the first stage, resulting in the metallic Ti and V on the surface, and the oxygen of the Zr-oxide and/or Zr sub-oxides diffuse to the interior of the coating in the continuous temperature rise, resulting in the metallic Zr on the surface. It is further suggested that the deterioration of the Ti-Zr-V NEG coating means the Zr and secondary Ti are oxidized deep into the coating, resulting in the restriction of the oxygen migration from the NEG compositions on the surface and consequently the lack of surface metallization.

Journal Articles

Flexible waste management system for the future application of MA P&T technology to the current high-level liquid waste

Fukasawa, Tetsuo*; Suzuki, Akihiro*; Endo, Yoichi*; Inagaki, Yaohiro*; Arima, Tatsumi*; Muroya, Yusa*; Endo, Keita*; Watanabe, Daisuke*; Matsumura, Tatsuro; Ishii, Katsunori; et al.

Journal of Nuclear Science and Technology, 61(3), p.307 - 317, 2024/03

 Times Cited Count:2 Percentile:27.70(Nuclear Science & Technology)

A flexible waste management system (FWM) is being developed to apply future MA partitioning and transmutation (P&T) technology to current HLLW. This FWM system will store high-level waste (HLLW) in granular form until MA partitioning and transmutation technology is realized. The feasibility of the main process was essentially confirmed by basic experiments and preliminary thermal analysis for granule production by rotary kiln from simulated HLLW and for temporary storage (50 years) of HLW granules at the HLW storage facility, respectively. The granule production experiments revealed that relatively large particles can be produced by the rotary kiln. The results of the thermal analysis showed that the small diameter canisters could be used to safely store the granules at a higher storage density than vitrified HLW. The effectiveness of the FWM system in terms of potential radiotoxicity and repository area was also evaluated, and it was shown that FWM can reduce these factors and has significant advantages in the disposal of HLW generated in current reprocessing plants. Since LWR fuel is stored for a long period of time in Japan and the operation of a reprocessing plant is expected to start soon, the FWM system is considered to be an effective system for reducing the environmental burden of HLW disposal.

Journal Articles

Decontamination and solidification treatment on spent liquid scintillation cocktail

Watanabe, So; Takahatake, Yoko; Ogi, Hiromichi*; Osugi, Takeshi; Taniguchi, Takumi; Sato, Junya; Arai, Tsuyoshi*; Kajinami, Akihiko*

Journal of Nuclear Materials, 585, p.154610_1 - 154610_6, 2023/11

 Times Cited Count:0 Percentile:0.00(Materials Science, Multidisciplinary)

642 (Records 1-20 displayed on this page)