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Journal Articles

Development of multi-purpose MW gyrotrons for fusion devices

Minami, Ryutaro*; Kariya, Tsuyoshi*; Imai, Tsuyoshi*; Numakura, Tomoharu*; Endo, Yoichi*; Nakabayashi, Hidetaka*; Eguchi, Taku*; Shimozuma, Takashi*; Kubo, Shin*; Yoshimura, Yasuo*; et al.

Nuclear Fusion, 53(6), p.063003_1 - 063003_7, 2013/06

Journal Articles

Development of multi-purpose MW gyrotrons for fusion devices

Minami, Ryutaro*; Kariya, Tsuyoshi*; Imai, Tsuyoshi*; Numakura, Tomoharu*; Endo, Yoichi*; Nakabayashi, Hidetaka*; Eguchi, Taku*; Shimozuma, Takashi*; Kubo, Shin*; Yoshimura, Yasuo*; et al.

Nuclear Fusion, 53(6), p.063003_1 - 063003_7, 2013/06

 Times Cited Count:12 Percentile:42.02(Physics, Fluids & Plasmas)

Journal Articles

Adsorption of Nb, Ta and Pa on anion-exchanger in HF and HF/HNO$$_{3}$$ solutions; Model experiments for the chemical study of Db

Kasamatsu, Yoshitaka; Toyoshima, Atsushi; Haba, Hiromitsu*; Tome, Hayato*; Tsukada, Kazuaki; Akiyama, Kazuhiko*; Yoshimura, Takashi*; Nagame, Yuichiro

Journal of Radioanalytical and Nuclear Chemistry, 279(2), p.371 - 376, 2009/02

 Times Cited Count:11 Percentile:35.15(Chemistry, Analytical)

Anion-exchange behavior of the group-5 elements Nb and Ta, and their pseudo homologue Pa in HF and HF/HNO$$_{3}$$ solutions was investigated by a batch method to find suitable conditions for the anion-exchange experiment of element 105 (Dubnium, Db). We determined distribution coefficients of those elements on the anion-exchange resin as a function of the F$$^{-}$$ and NO$$_{3}$$$$^{-}$$ concentrations. Clearly different anion-exchange behavior was observed among these elements. Based on the results, we discuss the fluoro-complex formation of each element and suggest experimental conditions for the study of fluoride complexation of Db.

Journal Articles

Startup of superheavy element chemistry at RIKEN

Haba, Hiromitsu*; Akiyama, Takahiro*; Kaji, Daiya*; Kikunaga, Hidetoshi*; Kuribayashi, Takahiro*; Morimoto, Koji*; Morita, Kosuke*; Oe, Kazuhiro*; Sato, Nozomi*; Shinohara, Atsushi*; et al.

European Physical Journal D, 45(1), p.81 - 86, 2007/10

 Times Cited Count:9 Percentile:53.24(Optics)

A review is given on the startup of the superheavy element (SHE) chemistry at RIKEN. A gas-jet transport system for the SHE chemistry has been coupled to the gas-filled recoil ion separator GARIS at the RIKEN Linear Accelerator. The performance of the system was appraised using $$^{206}$$Fr and $$^{245}$$Fm produced in the $$^{169}$$Tm($$^{40}$$Ar,3${it n}$)$$^{206}$$Fr and $$^{208}$$Pb($$^{40}$$Ar,3${it n}$)$$^{245}$$Fm reactions, respectively. The $$alpha$$ particles of $$^{206}$$Fr and $$^{245}$$Fm separated with GARIS and transported by the gas-jet were identified with a rotating wheel system for $$alpha$$ spectrometry under desired low background condition. The high gas-jet efficiencies over 80% were independent of the beam intensities up to 2 particle $$mu$$A. A gas-jet coupled target system for the production of SHEs was also installed on the beam line of the RIKEN K70 AVF cyclotron. The gas-jet transport of $$^{255}$$No and $$^{261}$$Rf produced in the $$^{238}$$U($$^{22}$$Ne,5${it n}$)$$^{255}$$No and $$^{248}$$Cm($$^{18}$$O,5${it n}$)$$^{261}$$Rf reactions, respectively, was conducted for the future chemical studies of $$^{265}$$Sg via the $$^{248}$$Cm($$^{22}$$Ne, 5${it n}$)$$^{265}$$Sg reaction.

Journal Articles

"Crystal lattice engineering", an approach to engineer protein crystal contacts by creating intermolecular symmetry; Crystallization and structure determination of a mutant human RNase 1 with a hydrophobic interface of leucines

Yamada, Hidenori*; Tamada, Taro; Kosaka, Megumi*; Miyata, Kohei*; Fujiki, Shinya*; Tano, Masaru*; Moriya, Masayuki*; Yamanishi, Mamoru*; Honjo, Eijiro; Tada, Horiko*; et al.

Protein Science, 16(7), p.1389 - 1397, 2007/07

 Times Cited Count:32 Percentile:42.53(Biochemistry & Molecular Biology)

In an attempt to control protein incorporation in a crystal lattice, a leucine zipper-like hydrophobic interface (comprising four leucine residues) was introduced into a helical region (helix 2) of the human pancreatic ribonuclease 1 (RNase 1) that was predicted to form a suitable crystallization interface. Although crystallization of wild type RNase 1 has not yet been reported, the RNase 1 mutant having four leucines (4L-RNase 1) was successfully crystallized under several different conditions. The crystal structures were subsequently determined by X-ray crystallography by molecular replacement using the structure of bovine RNase A. The overall structure of 4L-RNase 1 is quite similar to that of the bovine RNase A, and the introduced leucine residues formed the designed crystal interface. To further characterize the role of the introduced leucine residues in crystallization of RNase 1, the number of leucines was reduced to three or two (3L- and 2L-RNase 1, respectively). Both mutants crystallized and a similar hydrophobic interface as in 4L-RNase 1 was observed. A related approach to engineer crystal contacts at helix 3 of RNase 1 (N4L-RNase 1) was also evaluated. N4L-RNase 1 also successfully crystallized, and formed the expected hydrophobic packing interface. These results suggest that appropriate introduction of a leucine zipper-like hydrophobic interface can promote intra molecular symmetry for more efficient protein crystallization in crystal lattice engineering efforts.

Journal Articles

Studies of fast-ion transport induced by energetic particle modes using fast-particle diagnostics with high time resolution in CHS

Isobe, Mitsutaka*; Toi, Kazuo*; Matsushita, Hiroyuki*; Goto, Kazuyuki*; Suzuki, Chihiro*; Nagaoka, Kenichi*; Nakajima, Noriyoshi*; Yamamoto, Satoshi*; Murakami, Sadayoshi*; Shimizu, Akihiro*; et al.

Nuclear Fusion, 46(10), p.S918 - S925, 2006/10

 Times Cited Count:25 Percentile:31.65(Physics, Fluids & Plasmas)

no abstracts in English

Journal Articles

Beam-palarization asymmetries for the $$p$$($$overrightarrow{gamma}$$,$$K$$$$^{+}$$)$$Lambda$$ and $$p$$($$overrightarrow{gamma}$$,$$K$$$$^{+}$$)$$Sigma$$$$^{0}$$ reactions for $$E$$$$_{gamma}$$=1.5-2.4 GeV

Zegers, R. G. T.*; Sumihama, Mizuki*; Ahn, D. S.*; Ahn, J. K.*; Akimune, Hidetoshi*; Asano, Yoshihiro; Chang, W. C.*; Dat$'e$, S.*; Ejiri, Hiroyasu*; Fujimura, Hisako*; et al.

Physical Review Letters, 91(9), p.092001_1 - 092001_4, 2003/08

 Times Cited Count:125 Percentile:4.58(Physics, Multidisciplinary)

no abstracts in English

Journal Articles

Evidence for a narrow $$S$$ = +1 Baryon resonance in photoproduction from the neutron

Nakano, Takashi*; Ahn, D. S.*; Ahn, J. K.*; Akimune, Hidetoshi*; Asano, Yoshihiro; Chang, W. C.*; Date, S.*; Ejiri, Hiroyasu*; Fujimura, Hisako*; Fujiwara, Mamoru; et al.

Physical Review Letters, 91(1), p.012002_1 - 012002_4, 2003/07

 Times Cited Count:984 Percentile:0.11(Physics, Multidisciplinary)

no abstracts in English

Oral presentation

Alpha radioactivity measurement technology with ionized air type measurement apparatus, 2; Measurement test for decontaminated components

Mita, Yutaka; Matsumura, Toshihiro; Sugitsue, Noritake; Yamaguchi, Hiromi; Sano, Akira*; Naito, Susumu*; Maekawa, Tatsuyuki*; Yoshimura, Yukio*; Matsumoto, Takashi*

no journal, , 

By using Ionized Air Type Measurement Apparatus which was designed to measure clearance level of dismantled large-scale things which generate from nuclear plants, after chemical decontaminating machinery and materials which are used in plants, we experimented on a real-scale measurement of clearance level of them. We evaluated performance of detection and confirm applicability as a system of measurement of clearance level.

Oral presentation

Inspection and repair techniques in reactor vessel of sodium cooled fast reactor, 5; Visual inspection and obstacle removal method in reactor vessel of the experimental fast reactor Joyo

Ito, Hideaki; Nagai, Akinori; Tobita, Shigeharu; Ashida, Takashi; Kaito, Yasuaki; Katagiri, Genichi*; Kodama, Takemitsu*; Yoshimura, Tetsuji*

no journal, , 

no abstracts in English

Oral presentation

Influence of ground motion to the linac tunnel, 3; Long-period strong ground motion

Yoshimura, Aya*; Ichimura, Takahito; Kitami, Takayuki; Horiguchi, Takashi; Kawama, Itsuo*; Ouchi, Hajime*; Tsunokake, Hisao*

no journal, , 

no abstracts in English

Oral presentation

Quest for microorganisms existing at high atmosphere and space

Yokobori, Shinichi*; Yang, Y.*; Sugino, Tomohiro*; Kawaguchi, Yuko*; Itahashi, Shiho*; Fujisaki, Kenta*; Fushimi, Hidehiko*; Hasegawa, Sunao*; Hashimoto, Hirofumi*; Hayashi, Nobuhiro*; et al.

no journal, , 

Oral presentation

Solvent extraction of heavy actinides (III) with HDEHP

Takayama, Reona*; Oe, Kazuhiro*; Komori, Yukiko*; Fujisawa, Hiroyuki*; Kuriyama, Ai*; Kikutani, Yuki*; Kikunaga, Hidetoshi*; Kasamatsu, Yoshitaka*; Yoshimura, Takashi*; Takahashi, Naruto*; et al.

no journal, , 

The extraction behavior of trivalent actinides (Am, Cm, Cf, Es, and Fm) into di(2-ethylhexyl)phosphoric acid, HDEHP, in benzene from HNO$$_{3}$$ was studied together with lanthanides. The extraction constants, $$it K$$$$_{ex}$$ values, of lanthanides, Am, Cm, Cf, and Es were determined by a batch method using stable lanthanide isotopes and radiotracers of $$^{241}$$Am, $$^{243}$$Cm, $$^{249}$$Cf, and $$^{253}$$Es, respectively, while that of Fm was measured with $$^{250}$$Fm which was produced in the $$^{238}$$U($$^{16}$$O,4n) reaction and was on-line supplied by a gas-jet method at the AVF cyclotron of RCNP, Osaka University. The $$it K$$$$_{ex}$$ values were determined by the slope analysis for the variation of the distribution ratio as a function of the concentration of HDEHP. We found that the $$it K$$$$_{ex}$$of Fm is smaller than that of Dy in spite of the similar ionic radii while those of other actinides are almost the same as those of each lanthanide with a similar ionic radius.

Oral presentation

Microbes capture and expose experiments on ISS proposed in Tanpopo mission

Kawaguchi, Yuko*; Sugino, Tomohiro*; Yang, Y.*; Takahashi, Yuta*; Yoshimura, Yoshitaka*; Tsuji, Takashi*; Kobayashi, Kensei*; Tabata, Makoto*; Hashimoto, Hirofumi*; Narumi, Issei; et al.

no journal, , 

no abstracts in English

Oral presentation

Extraction of molybdenum and tungsten in oxidation state +5 and +6 from hydrochloric acid with Aliquat 336

Yokokita, Takuya*; Komori, Yukiko*; Kikutani, Yuki*; Kino, Aiko*; Shiohara, Naoya*; Kasamatsu, Yoshitaka*; Yoshimura, Takashi*; Takahashi, Naruto*; Oe, Kazuhiro; Shinohara, Atsushi*

no journal, , 

We are planning to study a redox behavior of element 106, seaborgium (Sg) based on the comparison of the behaviors with those of molybdenum (Mo) and tungsten (W). In this work, we studied solvent extraction behaviors of Mo(VI), Mo(V), W(VI), and W(V) with Aliquat 336 from hydrochloric acid (HCl). Mo(V) is extracted with higher distribution ratios than those of Mo(VI) in 4 to 11 M HCl. Distribution ratios of Mo(V) obtained by reducing Mo(VI) electrochemically are in good agreement with those of [MoCl$$_5$$].

Oral presentation

Extraction behavior of Mo(VI), Mo(V), W(VI), and W(V) from HCl solutions by Aliquat 336

Yokokita, Takuya*; Oe, Kazuhiro; Komori, Yukiko*; Kikutani, Yuki*; Kino, Aiko*; Nakamura, Kohei*; Kasamatsu, Yoshitaka*; Takahashi, Naruto*; Yoshimura, Takashi*; Takamiya, Koichi*; et al.

no journal, , 

We carried out solvent extraction of Mo(VI), Mo(V), W(VI) and W(V) in 0.01-0.36 M Aliquat 336 / 0.1-11 M HCl system as model experiments for element 106, seaborgium (Sg). The HCl solutions of Mo(VI), Mo(V), W(VI) and W(V) were prepared using macro amounts of Mo and W. Extraction behaviors of mononuclear Mo and W were also investigated using carrier-free radiotracers $$^{99}$$Mo and $$^{181}$$W, which were produced as $$^{235}$$U(n, f) and $$^{181}$$Ta (p, n) reaction, respectively. The distribution ratios (D) of Mo(V) and W(V) were higher than those of Mo(VI) and W(VI), respectively. These results suggest that reduction behavior of the group-6 elements can be observed by solvent extraction. The D values of carrier-free Mo(VI) and W(VI) are almost the same as those with macro amounts in 6-11 M HCl. This condition would be suitable for the Sg experiments.

Oral presentation

Mechanistic study on radiation-induced graft polymerization into a fluorinated polymer film

Ko, B.-S.*; Hasegawa, Shin; Hamada, Takashi; Yoshimura, Kimio; Maekawa, Yasunari

no journal, , 

Oral presentation

Decomposition behavior of radiation graft-type anion exchange membranes in an aqueous alkali solution

Takeuchi, Kota*; Hamada, Takashi; Yoshimura, Kimio; Hiroki, Akihiro; Maekawa, Yasunari

no journal, , 

no abstracts in English

Oral presentation

Mapping project in Fukushima and related researches, 1; Summary on temporal change of air dose rates and radionuclide deposition densities in the 80 km zone

Saito, Kimiaki; Mikami, Satoshi; Ando, Masaki; Matsuda, Norihiro; Tsuda, Shuichi; Yoshida, Tadayoshi; Yoshimura, Kazuya; Sato, Tetsuro*; Kanno, Takashi; Yamamoto, Hideaki

no journal, , 

no abstracts in English

Oral presentation

Redox and solvent extraction behavior of astatine

Toyoshima, Atsushi; Kanda, Akimitsu*; Ikeda, Takumi*; Yoshimura, Takashi*; Shinohara, Atsushi*; Yano, Shinya*; Komori, Yukiko*; Haba, Hiromitsu*

no journal, , 

Astatine (At) is reported to be bound in a few oxidation states in aqueous solutions. However, their valencies and chemical species are experimentally not identified. In this study, we studied redox behavior of At using redox agents and using a flow electrolytic column. $$^{211}$$At was produced in the $$^{209}$$Bi($$alpha$$, 2${it n}$)$$^{211}$$At reaction and was then separated from the target by a distillation method. Then, redox of At was carried out in 1.0 M HClO$${_4}$$ using redox agents or by an electrolysis. After the redox, solvent extraction with HDEHP was performed to identify the redox reactions. Using the redox agents, extraction yields of At were different between the conditions with oxidizing or reducing agents and without redox agents. This means that redox reactions of At can be identified under the present extraction conditions. On the other hand, by the electrolysis, extraction yields of At were almost constant against the variation of applied potential. This is possibly due to the restoration to the original oxidation state after the electrolysis. In the future, we will perform flow electrolytic column chromatography available for simultaneous electrolysis and separation.

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