Position dependency of the scattered intensity in the time-of-flight backscattering spectrometer DNA

Matsuura, Masato*; Yamada, Takeshi*; Tominaga, Taiki*; Kobayashi, Makoto*; Nakagawa, Hiroshi; Kawakita, Yukinobu

JPS Conference Proceedings (Internet), 33, p.011068_1 - 011068_6, 2021/03

https://doi.org/10.7566/JPSCP.33.011068

The position dependence of the scattered intensity in the time-of-flight backscattering spectrometer DNA was investigated. A periodic structure for both vertical (pixel) and horizontal (PSD) directions was observed. The solar slit and over-bending of an analyzer crystal is discussed as a possible origin of the modulation in the intensity. We have developed software program for the systematic correction of the position-dependent intensity and offset energy for the elastic peak. This corrects the deviation from the true scattering intensity and improve the quality of the data, which includes the energy resolution.

Analytical data on contaminated water, rubble and other collected at the Fukushima Daiichi Nuclear Power Station

Asami, Makoto*; Takahatake, Yoko; Myodo, Masato; Tobita, Takeshi; Kobayashi, Kiwami; Hayakawa, Misa; Usui, Yuka; Watahiki, Hiromi; Shibata, Atsuhiro; Nomura, Kazunori; et al.

JAEA-Data/Code 2017-001, 78 Pages, 2017/03

JAEA-Data-Code-2017-001.pdf:4.92MB
JAEA-Data-Code-2017-001-appendix(DVD-ROM).zip:818.06MB

At Fukushima Daiichi Nuclear Power Station owned by Tokyo Electric Power Company Holdings, Incorporated (TEPCO), contaminated water (accumulated, treated) secondary waste from water treatment, rubble and soil were collected and analyzed. The data already opened to public was collected as this report. The analytical data reported by TEPCO, Japan Atomic Energy Agency and International Research Institute for Nuclear Decommissioning until the end of March, 2016, was collected. Information on the samples and values of radioactive nuclide concentration and others were tabulated, besides figures, which show change in radioactive nuclide concentration for major nuclides, are contained. And, English translation and the collected data are provided as electric data.

Ni synchrotron radiation-based Mssbauer spectroscopy of nickel-based nanoparticles with hexagonal structure

Masuda, Ryo*; Kobayashi, Yasuhiro*; Kitao, Shinji*; Kurokuzu, Masayuki*; Saito, Makina*; Yoda, Yoshitaka*; Mitsui, Takaya; Hosoi, Kohei*; Kobayashi, Hirokazu*; Kitagawa, Hiroshi*; et al.

Scientific Reports (Internet), 6, p.20861_1 - 20861_8, 2016/02

https://doi.org/10.1038/srep20861

NHEJ repair rather than HR repair is the primary function to target to enhance radiosensitization at high LET values

Takahashi, Akihisa*; Kubo, Makoto*; Igarashi, Chie*; Yoshida, Yukari*; Funayama, Tomoo; Kobayashi, Yasuhiko; Nakano, Takashi*

JAEA-Review 2014-050, JAEA Takasaki Annual Report 2013, P. 82, 2015/03

https://doi.org/10.11484/jaea-review-2014-050

DNA double-strand breaks (DSBs) induced by ionizing radiation pose a major threat to cell survival. The cell can respond to the presence of DSBs, through two major repair pathways: Homologous recombination (HR) and non-homologous end-joining (NHEJ). Higher levels of cell death are induced by high-LET radiation when compared to low-LET radiation, even at the same doses because of less effective or more inefficient DNA repair. In this study, we examine the effects of radiation with different LET values on DNA DSB repair and radiosensitivity. Wild-type cells and HR deficient (but NHEJ proficient) cells exhibited the high RBE values at LET values of 108 keV/ m. The RBE value for each cell type decreased with increasing LET values over 200 keV/m. Although NHEJ proficient cells had an almost constant SER value, NHEJ deficient cells showed a high SER value when compared to NHEJ proficient cells, even with increasing LET values.

Nonhomologous end-joining repair plays a more important role than homologous recombination repair in defining radiosensitivity after exposure to high-LET radiation

Takahashi, Akihisa*; Kubo, Makoto*; Ma, H.*; Nakagawa, Akiko*; Yoshida, Yukari*; Isono, Mayu*; Kanai, Tatsuaki*; Ono, Tatsuya*; Furusawa, Yoshiya*; Funayama, Tomoo; et al.

Radiation Research, 182(3), p.338 - 344, 2014/09

https://doi.org/10.1667/RR13782.1

To clarify whether high-LET radiation inhibits all repair pathways or specifically one repair pathway, studies were designed to examine the effects of radiation with different LET values on DNA DSB repair and radiosensitivity. Embryonic fibroblasts bearing repair gene KO were exposed to X rays, carbon-, iron-, neon- and argon-ion beams. Cell survival was measured with colony-forming assays. The sensitization enhancement ratio (SER) values were calculated using the 10% survival dose of wild-type cells and repair-deficient cells. Cellular radiosensitivity was listed in descending order: double-KO cells NHEJ-KO cells HR-KO cells wild-type cells. Although HR-KO cells had an almost constant SER value, NHEJ-KO cells showed a high-SER value when compared to HR-KO cells, even with increasing LET values. These results suggest that with carbon-ion therapy, targeting NHEJ repair yields higher radiosensitivity than targeting homologous recombination repair.

Development of extraction chromatographic adsorbent using alkylpyridinedicarboxyamides as extractant for separation of trivalent minor actinides from lanthanides; Stability and separation ability against nitric acid exposure and -ray irradiation

Arisaka, Makoto; Watanabe, Masayuki; Sugo, Yumi; Kobayashi, Kumiko*; Kanao, Osamu*; Kimura, Takaumi

Journal of Nuclear Science and Technology, 51(4), p.457 - 464, 2014/04

https://doi.org/10.1080/00223131.2014.874301

Toward the development of a practical separation method for trivalent actinides and lanthanides, we used extraction chromatography with alkyl-pyridinedicarboxyamides as the extractant. The results confirmed that the performance degradation of the adsorbent caused by contact with HNO and/or irradiation with rays would be very small during the operation of column chromatography. The optimal conditions for the column separation were also determined: eluent, 5M HNO; flow rate, 0.1 mL/min.

Monitoring of airborne C discharge at RI facilities; A Comparison of collection and oxidation methods

Ueno, Yumi; Koarashi, Jun; Iwai, Yasunori; Sato, Junya; Takahashi, Teruhiko; Sawahata, Katsunori; Sekita, Tsutomu; Kobayashi, Makoto; Tsunoda, Masahiko; Kikuchi, Masamitsu

Hoken Butsuri, 49(1), p.39 - 44, 2014/03

http://doi.org/10.5453/jhps.49.39

http://doi.org/10.5453/jhps.49.2

The Japan Atomic Energy Agency has conducted a monthly monitoring of airborne C discharge at the forth research building (RI facility) of the Tokai Research and Development Center. In the current monitoring, C, which exists in various chemical forms in airborne effluent, is converted into CO with CuO catalyst and then collected using monoethanolamine (MEA) as CO absorbent. However, this collection method has some issues on safety management because the CuO catalyst requires a high heating temperature (600C) to ensure a high oxidation efficiency and the MEA is specified as a poisonous and deleterious substance. To establish a safer, manageable and reliable method for monitoring airborne C discharge, we examined collection methods that use different CO absorbents (MEA and Carbo-Sorb E) and oxidation catalysts (CuO, Pt/Alumina and Pd/ZrO). The results showed 100% CO collection efficiency of MEA during a 30-day sampling period under the condition tested. In contrast, Carbo-Sorb E was found to be unsuitable for the monthly-long CO collection because of its high volatile nature. Among the oxidation catalysts, the Pd/ZrO showed the highest oxidation efficiency for CH at a lower temperature.

Investigation of advanced divertor magnetic configuration for DEMO tokamak reactor

Asakura, Nobuyuki; Shinya, Kichiro*; Tobita, Kenji; Hoshino, Kazuo; Shimizu, Katsuhiro; Uto, Hiroyasu; Someya, Yoji; Nakamura, Makoto; Ono, Noriyasu*; Kobayashi, Masahiro*; et al.

Fusion Science and Technology, 63(1T), p.70 - 75, 2013/05

https://doi.org/10.13182/FST13-A16876

no abstracts in English

Probing carbon edge exposure of iron phthalocyanine-based oxygen reduction catalysts by soft X-ray absorption spectroscopy

Niwa, Hideharu*; Saito, Makoto*; Kobayashi, Masaki*; Harada, Yoshihisa*; Oshima, Masaharu*; Moriya, Shogo*; Matsubayashi, Katsuyuki*; Nabae, Yuta*; Kuroki, Shigeki*; Ikeda, Takashi; et al.

Journal of Power Sources, 223, p.30 - 35, 2013/02

https://doi.org/10.1016/j.jpowsour.2012.09.031

To design non-platinum, inexpensive, but high performance carbon-based cathode catalysts for polymer electrolyte fuel cells, it is important to elucidate the active site for oxygen reduction reaction (ORR). However, it is difficult to directly identify the active site by applying conventional structural or electronic probes to such complex systems. Here, we used C 1 X-ray absorption spectroscopy (XAS) to observe electronic structure of carbon in iron phthalocyanine-based catalysts, and found a signature of edge exposure below the edge, whose intensity is well correlated with the ORR activity. These results demonstrate that C 1 XAS can be used to characterize the ORR activity of carbon-based cathode catalysts in terms of the edge exposure.

Indirect contribution of transition metal towards oxygen reduction reaction activity in iron phthalocyanine-based carbon catalysts for polymer electrolyte fuel cells

Kobayashi, Masaki*; Niwa, Hideharu*; Saito, Makoto*; Harada, Yoshihisa*; Oshima, Masaharu*; Ofuchi, Hironori*; Terakura, Kiyoyuki*; Ikeda, Takashi; Koshigoe, Yuka*; Ozaki, Junichi*; et al.

Electrochimica Acta, 74, p.254 - 259, 2012/07

https://doi.org/10.1016/j.electacta.2012.04.075

The electronic structure of the residual metal atoms in FePc-based carbon catalysts, prepared by pyrolyzing a mixture of FePc and phenolic resin polymer at 800C, before and after acid washing have been investigated using XAFS spectroscopy to clarify the role of Fe in the ORR activity. The decomposition analyses for the XAFS spectra reveal that the composition ratio of each Fe component is unaltered by the acid washing, indicating that the residual Fe components were removed by the acid washing irrespective of their chemical states. Because the oxygen reduction potential was approximately unchanged by the acid washing, the residual Fe itself does not seem to contribute directly to the ORR activity. The residual Fe can act as a catalyst to accelerate the growth of the sp carbon network during pyrolysis. The results imply that light elements are components of the ORR active sites in the FePc-based carbon catalysts.