Shimojo, Kojiro; Fujiwara, Iori*; Oshima, Tatsuya*; Yokoyama, Keiichi; Yaita, Tsuyoshi
Analytical Sciences, 38(7), p.1003 - 1006, 2022/07
Liquid-liquid extraction of lanthanide (Ln) ions was investigated using -dioctylthiodiglycolamic acid (DOTDGAA), which is a sulfur donor ligand with an amide group and a carboxyl group connected by a thioether chain. The extraction performance and selectivity of DOTDGAA for Ln ions were compared with those of -dioctyldiglycolamic acid (DODGAA), which is also an oxygen donor ligand with a similar chemical structure, to assess the effect of the soft/hard donor atom on Ln separation. DOTDGAA quantitatively extracted all Ln ions while being selective toward light and middle Ln ions, in contrast to the selectivity of DODGAA for heavier Ln ions. Slope analysis demonstrated that the Ln transfer using DOTDGAA proceeded through a proton-exchange reaction, forming a 1:3 complex, Ln(DOTDGAA). The back-extraction of Ln ions from the extracting phase was successfully achieved under acidic conditions.
Matsuda, Shohei; Yokoyama, Keiichi; Yaita, Tsuyoshi; Kobayashi, Toru; Kaneta, Yui; Simonnet, M.; Sekiguchi, Tetsuhiro; Honda, Mitsunori; Shimojo, Kojiro; Doi, Reisuke; et al.
Science Advances (Internet), 8(20), p.eabn1991_1 - eabn1991_11, 2022/05
no abstracts in English
Yamaguchi, Akiko; Nagata, Kojiro*; Tanaka, Kazuya; Kobayashi, Keita; Kobayashi, Toru; Shimojo, Kojiro; Tanida, Hajime; Sekiguchi, Tetsuhiro; Kaneta, Yui; Matsuda, Shohei; et al.
Hosha Kagaku, (45), p.28 - 30, 2022/03
no abstracts in English
Simonnet, M.; Kobayashi, Toru; Shimojo, Kojiro; Yokoyama, Keiichi; Yaita, Tsuyoshi
Inorganic Chemistry, 60(17), p.13409 - 13418, 2021/09
Go, Shintaro*; Ideguchi, Eiji*; Yokoyama, Rin*; Aoi, Nori*; Azaiez, F.*; Furutaka, Kazuyoshi; Hatsukawa, Yuichi; Kimura, Atsushi; Kisamori, Keiichi*; Kobayashi, Motoki*; et al.
Physical Review C, 103(3), p.034327_1 - 034327_8, 2021/03
Shimojo, Kojiro; Suzuki, Hideya; Yokoyama, Keiichi; Yaita, Tsuyoshi; Ikeda, Atsushi
Analytical Sciences, 36(12), p.1435 - 1437, 2020/12
Liquid-liquid extraction for the removal of pertechnetate (TcO) and perrhenate (ReO) is reported using tripodal extractant -hexa--octylnitrilotriacetamide (HONTA) composed of three amide groups and a tertiary amine. The extraction behavior was compared with those using alkyldiamideamines (ADAAM(Oct) and ADAAM(EH)), and the commercial amine-type extractant, trioctylamine (TOA). HONTA quantitatively extracted TcO and ReO in the pH range from 1.0 to 2.5 by co-extraction of protons. Extraction performance of extractants was improved in the order of HONTA ADAAM(Oct) ADAAM(EH) TOA. TcO and ReO in the extracting phase were successfully stripped using neutral aqueous solutions as the receiving phase, and the extraction ability of HONTA was maintained after five repeated uses.
Tang, T. L.*; Uesaka, Tomohiro*; Kawase, Shoichiro; Beaumel, D.*; Dozono, Masanori*; Fujii, Toshihiko*; Fukuda, Naoki*; Fukunaga, Taku*; Galindo-Uribarri, A.*; Hwang, S. H.*; et al.
Physical Review Letters, 124(21), p.212502_1 - 212502_6, 2020/05
The structure of a neutron-rich F nucleus is investigated by a quasifree () knockout reaction. The sum of spectroscopic factors of orbital is found to be 1.0 0.3. The result shows that the O core of F nucleus significantly differs from a free O nucleus, and the core consists of 35% O, and 65% excited O. The result shows that the O core of F nucleus significantly differs from a free O nucleus. The result may infer that the addition of the proton considerably changes the neutron structure in F from that in O, which could be a possible mechanism responsible for the oxygen dripline anomaly.
Simonnet, M.; Suzuki, Shinichi; Miyazaki, Yuji*; Kobayashi, Toru; Yokoyama, Keiichi; Yaita, Tsuyoshi
Solvent Extraction and Ion Exchange, 38(4), p.430 - 440, 2020/00
Kurosaki, Yuzuru*; Yokoyama, Keiichi
Universe (Internet), 5(5), p.109_1 - 109_15, 2019/05
Regarding rovibrational transitions of diatomic alkali haride molecules, optimal waveform of laser electric field was calculated on the basis of the optimal control theory. In this study, we implemented the polarizability term into the Hamiltonian, which defines the field-molecule interaction. As a result, we obtained waveforms causing both one- and two-photon processes in a relatively high electric field regime, while waveforms causing only one-photon process was observed in a weak filed regime as well as the previous study. These results imply that the effect of two-photon process is successfully taken into account in the optimal control theory calculation. Now we can expect more reliable calculation even for strong laser field.
Kobayashi, Takanori*; Matsuoka, Leo*; Yokoyama, Keiichi
Computational and Theoretical Chemistry, 1150, p.40 - 48, 2019/02
One of important research targets in the development of cesium isotope separation system is design of recovery process of cesium atom. Relevant to this research target, the reaction cross section and reaction rate constant of a cesium exchange reaction through collision of the cesium iodide molecules with cesium atoms are calculated by a quasi-classical trajectory calculation based on a potential energy surface obtained by quantum chemistry calculations. Consequently, the rate constant is calculated to be 3.6 10 cmmolecules, as large as collision rate in the present condition. In addition, slightly positive temperature dependence is observed in the rate constant. This behavior is explained with the long-range attractive force and effect of subsequent dissociation process.
Sekiguchi, Tetsuhiro; Yokoyama, Keiichi; Uozumi, Yuki*; Yano, Masahiro; Asaoka, Hidehito; Suzuki, Shinichi; Yaita, Tsuyoshi
Progress in Nuclear Science and Technology (Internet), 5, p.161 - 164, 2018/11
For nuclear transmutation of cesium-135 (Cs), which is long-lived fission product, we are developing selective absorbent which takes only Cs atom in, but does not CsI. In this study, absorbing property of Cs atom onto the surface of fullerene (C) film has been investigated using synchrotron-based angle-dependent X-ray photoelectron spectroscopy (XPS). The results were compared with those of CsI. It was found that Cs penetrates into C deep bulk. In contrast, CsI deposits on shallow surface. Furthermore, XPS spectra were measured as a function of Ar-sputtering time in order to know Cs concentration profiles in deep region. Results showed that Cs penetrates into deep region of several hundreds .
Kobayashi, Takanori*; Matsuoka, Leo*; Yokoyama, Keiichi
Nihon Enerugi Gakkai-Shi, 96(10), p.441 - 444, 2017/10
To investigate the reaction cross section of the cesium exchange reaction of CsI (v = 0, j = 0) + Cs Cs + ICs, we performed quasi-classical trajectory calculations on the potential energy surface calculated by the ab initio molecular orbital theory. The potential energy surface shows that intermediate CsI is formed without entrance barrier and has two equivalent Cs-I bonds. The reaction cross sections decrease monotonically with increasing collision energy. The rate constant k (v = 0, j = 0) was estimated to be about 310cm molecules at temperatures ranging from 500 to 1200K and a slight negative temperature dependence was observed.
Yokoyama, Sumi*; Hamada, Nobuyuki*; Hayashida, Toshiyuki*; Tsujimura, Norio; Tatsuzaki, Hideo*; Kurosawa, Tadahiro*; Nabatame, Kuniaki*; Oguchi, Hiroyuki*; Ono, Kazuko*; Kawaura, Chiyo*; et al.
Journal of Radiological Protection, 37(3), p.659 - 683, 2017/09
Since the International Commission on Radiological Protection recommended reducing the occupational equivalent dose limit for the lens of the eye in 2011, there have been extensive discussions in various countries. This paper reviews the current situations in radiation protection of the ocular lens and the discussions on the potential impact of the new lens dose limit in Japan. Topics include historical changes to the lens dose limit, the current situations in occupational lens exposures (e.g., in medical workers, nuclear workers, and Fukushima nuclear power plant workers) and measurements, and the current status of biological studies and epidemiological studies on radiation cataracts. Our focus is on the situations in Japan, but we believe such information sharing will be useful in many other countries.
Kurosaki, Yuzuru*; Yokoyama, Keiichi
Chemical Physics, 493, p.183 - 193, 2017/08
Electric field of laser pulses which gives maximum selectivity in the isotope-selective rovibrational excitation of lithium chloride molecules is calculated. Applying the optimal control theory, we calculate optimal electric field to produce mixture of LiCl-35 (=0, =0) and LiCl-37 (=1, =1) from molecular ensemble of LiCl-35 (=0, =0) and LiCl-37 (=0, =0). As a result, it is found that electric field which permit rotational excitations only gives high yield in the selective excitation compared to the electric field which permit both rotational and vibrational excitations.
Kobayashi, Takanori; Yokoyama, Keiichi
Journal of Nuclear Science and Technology, 53(10), p.1489 - 1493, 2016/10
Theoretical investigation for the adsorption of the cesium atom (Cs), the cesium iodide molecule (CsI), the iodine atom (I), the cesium cation (Cs), and the iodide anion (I) onto the surface of a single fullerene molecule (C) are reported. A hybrid exchange-correlation functional using the Coulomb-attenuating method (CAM-B3LYP) is employed. The adsorption energies, i.e., the opposite of enthalpy change through adsorption, are calculated to be 34, 3, 2, 11, and 12 kcal mol for Cs, CsI, I, Cs, and I, respectively. The equilibrium constant for Cs is calculated to be 710 atm at the temperature of 1000 K and is seven orders of magnitude higher than that for CsI, indicating that the C molecule adsorb the Cs atom highly selectively against the CsI molecule.
Kobayashi, Takanori; Hashimoto, Masashi; Yokoyama, Keiichi
JAEA-Research 2015-014, 7 Pages, 2015/12
To discuss the exchange reaction of Cs isotope by CsI + Cs' Cs + ICs', the structure and chemical properties of CsI intermediate and potential energy surface are calculated using M06/def2-TZVPPD density functional calculation. The calculation shows that the reaction to the intermediate has no barrier and the two Cs-I bonds of CsI are chemically equivalent. Thus, the collision of CsI + Cs' results in Cs exchange with the high probability.
Akahane, Keiichi*; Iimoto, Takeshi*; Ichiji, Takeshi*; Iwai, Satoshi*; Oguchi, Hiroyuki*; Ono, Kazuko*; Kawaura, Chiyo*; Kurosawa, Tadahiro*; Tatsuzaki, Hideo*; Tsujimura, Norio; et al.
Hoken Butsuri, 50(4), p.257 - 261, 2015/12
In a mixed field of photon and beta radiations, the same dose assigned to skin is normally assigned to the dose to the lens of the eye as a conservative estimate of H(3). In exceptional cases that a very high beta dose might be imparted of the same order with the dose limit, however, the conservatively biased dose must be too limiting, and thereby an accurate estimate of beta (3) is desirable. This article presents a practical proposal of when and how the dosimetry of beta (3) should be made.
Go, Shintaro*; Ideguchi, Eiji*; Yokoyama, Rin*; Kobayashi, Motoki*; Kisamori, Keiichi*; Takaki, Motonobu*; Miya, Hiroyuki*; Ota, Shinsuke*; Michimasa, Shinichiro*; Shimoura, Susumu*; et al.
JPS Conference Proceedings (Internet), 6, p.030005_1 - 030005_4, 2015/06
Ichihara, Akira; Matsuoka, Leo*; Segawa, Etsuo*; Yokoyama, Keiichi
Physical Review A, 91(4), p.043404_1 - 043404_7, 2015/04
We propose a new method for isotope-selective dissociation of diatomic molecules in the gas phase by using two kinds of terahertz-pulse fields. The first field consists of a train of pulses, which composes a frequency comb, excites the selected isotope into highly-rotationally excited state. The second intense pulse field dissociates the excited molecule by further rotational excitations. We performed wave-packet computations using the lithium chlorides LiCL and LiCl to demonstrate the applicability of our method. Nearly 20% of LiCl in the lowest rovibrational state is dissociated in the designed pulse fields, while the dissociation probability is negligible in LiCl. This method is expected to be applicable to other diatomic molecules, and to molecular ensembles whose rotational states spread in energy.
Ichihara, Akira; Matsuoka, Leo*; Kurosaki, Yuzuru; Yokoyama, Keiichi
Optical Review, 22(1), p.153 - 156, 2015/02
We propose a method to excite the rovibrational states of diatomic molecules in the gas-phase isotope-selectively by optical pulses. In this method, the rotational state of the selected isotope molecule is excited by the terahertz frequency comb, and the vibrational state of high J molecule is excited via the fundamental transitions in the P-branch by using the second pulse. The applicability of the proposed method is demonstrated by computer simulations using the LiCl molecules in the thermal distribution at 70 K.