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Journal Articles

Production of $$^{266}$$Bh in the $$^{248}$$Cm($$^{23}$$Na,5$$n$$)$$^{266}$$Bh reaction and its decay properties

Haba, Hiromitsu*; Fan, F.*; Kaji, Daiya*; Kasamatsu, Yoshitaka*; Kikunaga, Hidetoshi*; Komori, Yukiko*; Kondo, Narumi*; Kudo, Hisaaki*; Morimoto, Koji*; Morita, Kosuke*; et al.

Physical Review C, 102(2), p.024625_1 - 024625_12, 2020/08

 Times Cited Count:6 Percentile:59.56(Physics, Nuclear)

Journal Articles

Development of U and Pu co-processing process; Demonstration of U, Pu and Np Co-recovery with centrifugal contactors

Kudo, Atsunari; Kurabayashi, Kazuaki; Yanagibashi, Futoshi; Sasaki, Shunichi; Sato, Takehiko; Fujimoto, Ikuo; Obu, Tomoyuki

Proceedings of 2017 International Congress on Advances in Nuclear Power Plants (ICAPP 2017) (CD-ROM), 6 Pages, 2017/04

The Co-processing process is the extraction process to recover Pu/U mixed product solution with given Pu/U ratio for improving of nuclear proliferation resistance. In addition, Np is also recovered with U and Pu because Np is one of minor actinides and a long-lived radionuclide and Np has the extractability into TBP solvent. Development of its flowsheet achieves to decrease environmental effect of waste materials. The orientation of development about Co-processing process is to demonstrate of reprocessing the future spent fuels from a LWR, a LWR-MOX hybrid, and a FR-MOX with one cycle. We demonstrated by use of miniature reflux-type centrifugal contactors at the partitioning unit. The test conditions of the Pu/U ratio in the loaded solvents were 1%, 3%, and 5% considering the composition of spent fuels. We used the HAN as the reductant of Np (VI) for back extraction. The results of these tests were very good. We got the prospect of U, Pu, and Np Co-processing flowsheet.

Journal Articles

Complex chemistry with complex compounds

Eichler, R.*; Asai, Masato; Brand, H.*; Chiera, N. M.*; Di Nitto, A.*; Dressler, R.*; D$"u$llmann, Ch. E.*; Even, J.*; Fangli, F.*; Goetz, M.*; et al.

EPJ Web of Conferences, 131, p.07005_1 - 07005_7, 2016/12

 Times Cited Count:3 Percentile:72.98(Chemistry, Inorganic & Nuclear)

In recent years gas-phase chemical studies assisted by physical pre-separation allowed for the productions and investigations of fragile single molecular species of superheavy elements. The latest highlight is the formation of very volatile hexacarbonyl compound of element 106, Sg(CO)$$_{6}$$. Following this success, second-generation experiments were performed to measure the first bond dissociation energy between the central metal atom and the surrounding ligand. The method using a tubular decomposition reactor was developed and successfully applied to short-lived Mo(CO)$$_{6}$$, W(CO)$$_{6}$$, and Sg(CO)$$_{6}$$.

Journal Articles

Decomposition studies of group 6 hexacarbonyl complexes, 1; Production and decomposition of Mo(CO)$$_6$$ and W(CO)$$_6$$

Usoltsev, I.*; Eichler, R.*; Wang, Y.*; Even, J.*; Yakushev, A.*; Haba, Hiromitsu*; Asai, Masato; Brand, H.*; Di Nitto, A.*; D$"u$llmann, Ch. E.*; et al.

Radiochimica Acta, 104(3), p.141 - 151, 2016/03

 Times Cited Count:31 Percentile:95.03(Chemistry, Inorganic & Nuclear)

Conditions of the production and decomposition of hexacarbonyl complexes of short-lived Mo and W isotopes were investigated to study thermal stability of the heaviest group 6 hexacarbonyl complex Sg(CO)$$_6$$. A tubular flow reactor was tested to decompose the hexacarbonyl complexes and to extract the first bond dissociation energies. A silver was found to be the most appropriate reaction surface to study the decomposition of the group 6 hexacarbonyl. It was found that the surface temperature at which the decomposition occurred was correlated to the first bond dissociation energy of Mo(CO)$$_6$$ and W(CO)$$_6$$, indicating that the first bond dissociation energy of Sg(CO)$$_6$$ could be determined with this technique.

Journal Articles

Production of $$^{88}$$Nb and $$^{170}$$Ta for chemical studies of element 105, Db, using the GARIS gas-jet system

Huang, M.*; Haba, Hiromitsu*; Murakami, Masashi*; Asai, Masato; Kaji, Daiya*; Kanaya, Jumpei*; Kasamatsu, Yoshitaka*; Kikunaga, Hidetoshi*; Kikutani, Yuki*; Komori, Yukiko*; et al.

Journal of Radioanalytical and Nuclear Chemistry, 304(2), p.845 - 849, 2015/05

 Times Cited Count:3 Percentile:25.85(Chemistry, Analytical)

A technique to utilize radioisotopes of Nb and Ta was developed for chemical studies of element 105, Db, by coupling a gas-jet transport system to the RIKEN gas-filled recoil ion separator (GARIS). The short-lived $$^{88}$$Nb and $$^{170}$$Ta were produced with nuclear reactions using a $$^{19}$$F beam whose energy was the same as that to produce $$^{262}$$Db. Then, they were separated with GARIS and extracted to a chemistry laboratory with the gas-jet transport system. By changing only magnetic field of GARIS and inserting an energy degrader and a shutter for recoil ions, we could deliver the $$^{88}$$Nb and $$^{170}$$Ta to a chemistry device for $$^{262}$$Db without changing other experimental conditions.

Journal Articles

In situ synthesis of volatile carbonyl complexes with short-lived nuclides

Even, J.*; Ackermann, D.*; Asai, Masato; Block, M.*; Brand, H.*; Di Nitto, A.*; D$"u$llmann, Ch. E.*; Eichler, R.*; Fan, F.*; Haba, Hiromitsu*; et al.

Journal of Radioanalytical and Nuclear Chemistry, 303(3), p.2457 - 2466, 2015/03

 Times Cited Count:15 Percentile:77.56(Chemistry, Analytical)

Rapid In situ synthesis of metal carbonyl complexes has been demonstrated using short-lived isotopes produced in nuclear fission and fusion reactions. The short-lived isotopes with high recoil energy directly react with carbon-monoxides and form carbonyl complexes. Only highly volatile complexes were fast transported in a gas stream to counting and chemistry devices. Short-lived Mo, Tc, Ru, Rh, W, Re, Os, and Ir were found to form volatile carbonyl complexes, while no volataile complex of Hf and Ta were detected. This technique has been applied to a chemical investigation of the superheavy element Sg (atomic number 106), and will be applicable to various fields of nuclear science with short-lived transition metal isotopes.

Journal Articles

Synthesis and detection of a Seaborgium carbonyl complex

Even, J.*; Yakushev, A.*; D$"u$llmann, Ch. E.*; Haba, Hiromitsu*; Asai, Masato; Sato, Tetsuya; Brand, H.*; Di Nitto, A.*; Eichler, R.*; Fan, F. L.*; et al.

Science, 345(6203), p.1491 - 1493, 2014/09

 Times Cited Count:63 Percentile:83.28(Multidisciplinary Sciences)

A new superheavy element complex, a seaborgium carbonyl, has been successfully synthesized, and its adsorption property has been studied using a cryo-thermochromatography and $$alpha$$-detection apparatus COMPACT. Nuclear reaction products of short-lived $$^{265}$$Sg preseparated with a gas-filled recoil ion separator GARIS at RIKEN were directly injected into a gas cell filled with He/CO mixture gas, and chemical reaction products of volatile carbonyl complexes were trasported to COMPACT. The Sg carbonyl complex detected with COMPACT was found to be very volatile with adsorption enthalpy of $$-$$50 kJ/mol, from which we have concluded that this complex should be a Sg hexacarbonyl Sg(CO)$$_{6}$$. This is the first synthesis of organometallic compounds of transactinide elements for which only simple inorganic comounds have been synthesized so far.

Journal Articles

Production of $$^{262}$$Db in the $$^{248}$$Cm($$^{19}$$F,5$$n$$)$$^{262}$$Db reaction and decay properties of $$^{262}$$Db and $$^{258}$$Lr

Haba, Hiromitsu*; Huang, M.*; Kaji, Daiya*; Kanaya, Jumpei*; Kudo, Yuki*; Morimoto, Koji*; Morita, Kosuke*; Murakami, Masashi*; Ozeki, Kazutaka*; Sakai, Ryutaro*; et al.

Physical Review C, 89(2), p.024618_1 - 024618_11, 2014/02

 Times Cited Count:25 Percentile:82.3(Physics, Nuclear)

Journal Articles

Graft-type polymer electrolyte membranes for fuel cells prepared through radiation-induced graft polymerization into alicyclic polybenzimidazoles

Park, J.*; Takayama, Toshio*; Asano, Masaharu; Maekawa, Yasunari; Kudo, Kazuaki*; Takayama, Toshio*

Polymer, 54(17), p.4570 - 4577, 2013/08

 Times Cited Count:6 Percentile:19.37(Polymer Science)

Graft-type sulfonated polybenzimidazole was prepared through radiation-induced graft polymerization of styrenes into an alicyclic polybenzimidazole film and subsequent sulfonation. The alicyclic polybenzimidazole, ChPBI, was prepared from $$trans$$-1,4-cyclohexanedicarboxylic acid and 3,3'-diaminobenzidine using typical polycondensation. Anisotropic domains with a size of several tens of micrometers were found in the ChPBI films casted from LiCl-containing $$N$$,$$N$$-dimethylacetamide. Irradiation of the ChPBI membranes with a 220 kGy dose of $$gamma$$-rays created radical species with mean lifetimes of two days. The treatment of this membrane with a 50/50 (v/v) mixture of 1-propanol and styrene produced polystyrene graft chains. Sulfonation of the resulting grafted membrane with ClSOH$$_{3}$$OH occurred selectively on the polystyrene grafts. The sulfonated films showed proton conductivity on the order of 10$$^{-3}$$ to 10$$^{-2}$$ S/cm with an ion exchange capacity between 2.1 and 2.9 mmol/g. SEM-EDX analysis of the membrane indicated the presence of macrophase separated domains up to 1 $$mu$$m in diameter. The proton conductivity of the membrane did not decrease for 600 h at 120$$^{circ}$$C in liquid water.

Journal Articles

Sulfate complexation of element 104, Rf, in H$$_{2}$$SO$$_{4}$$/HNO$$_{3}$$ mixed solution

Li, Z.*; Toyoshima, Atsushi; Asai, Masato; Tsukada, Kazuaki; Sato, Tetsuya; Sato, Nozomi; Kikuchi, Takahiro; Nagame, Yuichiro; Sch$"a$del, M.; Pershina, V.*; et al.

Radiochimica Acta, 100(3), p.157 - 164, 2012/03

 Times Cited Count:13 Percentile:69.01(Chemistry, Inorganic & Nuclear)

Journal Articles

Production of $$^{265}$$Sg in the $$^{248}$$Cm($$^{22}$$Ne,5$$n$$)$$^{265}$$Sg reaction and decay properties of two isomeric states in $$^{265}$$Sg

Haba, Hiromitsu*; Kaji, Daiya*; Kudo, Yuki*; Morimoto, Koji*; Morita, Kosuke*; Ozeki, Kazutaka*; Sakai, Ryutaro*; Sumita, Takayuki*; Yoneda, Akira*; Kasamatsu, Yoshitaka*; et al.

Physical Review C, 85(2), p.024611_1 - 024611_11, 2012/02

 Times Cited Count:52 Percentile:91.35(Physics, Nuclear)

Two isomeric states in $$^{265}$$Sg, i.e, $$^{265}$$Sg$$^{a}$$ and $$^{265}$$Sg$$^{b}$$ were produced in the $$^{248}$$Cm($$^{22}$$Ne,5$$n$$) reaction. Decay properties of $$^{265}$$Sg$$^{a,b}$$ were investigated with a rotating-wheel apparatus for $$alpha$$ and spontaneous fission (SF) spectrometry under low background condition attained by a gas-jet transport system coupled to the RIKEN gas-filled recoil ion separator. Based on genetically correlated $$alpha$$-$$alpha$$ (-$$alpha$$) and $$alpha$$-SF decay chains, 18 and 24 events were assigned to $$^{265}$$Sg$$^{a}$$ and $$^{265}$$Sg$$^{b}$$, respectively. The half-life and $$alpha$$-particle energy of $$^{265}$$Sg$$^{a}$$ were measured to be $$8.5^{+2.6}_{-1.6}$$ s and $$8.84 pm 0.05$$ MeV, respectively, and those of $$^{265}$$Sg$$^{b}$$ were $$14.4^{+3.7}_{-2.5}$$ s and $$8.69 pm 0.05$$ MeV.

Journal Articles

Fluorido complex formation of element 104, rutherfordium (Rf)

Ishii, Yasuo; Toyoshima, Atsushi; Tsukada, Kazuaki; Asai, Masato; Li, Z.*; Nagame, Yuichiro; Miyashita, Sunao*; Mori, Tomotaka*; Suganuma, Hideo*; Haba, Hiromitsu*; et al.

Bulletin of the Chemical Society of Japan, 84(9), p.903 - 911, 2011/09

 Times Cited Count:17 Percentile:49.33(Chemistry, Multidisciplinary)

The cation-exchange behavior of element 104, rutherfordium (Rf), was investigated together with its lighter group-4 homologues Zr and Hf, and the tetravalent pseudo-homologue Th in HF/HNO$$_{3}$$ mixed solution. The results demonstrate that distribution coefficients ($$K_{d}$$) of Rf in HF/0.10 M HNO$$_{3}$$ decrease with increasing concentration of the fluoride ion [F$$^{-}$$], indicating the consecutive formation of fluorido complexes of Rf. We also measured the $$K_{d}$$ values of Rf and the homologues as a function of the hydrogen ion concentration [H$$^{+}$$]. The log $$K_{d}$$ values decrease linearly with an increase of log [H$$^{+}$$] with slopes between -2.1 and -2.5. This indicates that these elements are likely to form the same chemical compounds: mixture of [MF]$$^{3+}$$ and [MF$$_{2}$$]$$^{2+}$$ (M = Rf, Zr, Hf and Th) in the studied solution. It is also ascertained that sequence in the fluoride complex formation is Zr $$sim$$ Hf $$>$$ Rf $$>$$ Th.

Journal Articles

Extraction of chromatographic behavior of Rf, Zr, and Hf in HCl solution with styrenedivinylbenzene copolymer resin modified by TOPO (trioctylphosphine oxide)

Toyoshima, Atsushi; Kasamatsu, Yoshitaka*; Tsukada, Kazuaki; Asai, Masato; Ishii, Yasuo; Tome, Hayato*; Nishinaka, Ichiro; Sato, Tetsuya; Nagame, Yuichiro; Sch$"a$del, M.; et al.

Journal of Nuclear and Radiochemical Sciences, 11(1), p.7 - 11, 2010/06

The extraction behavior of rutherfordium (Rf) into trioctylphosphine oxide (TOPO) from 2.0 - 7.0 M HCl solution was studied together with that of the homologues Zr and Hf. The extracted yields of Rf, Zr, and Hf increased with an increase of HCl concentration, and the sequence of their extraction was Zr $$>$$ Hf $$geq$$ Rf. It is suggested that the stability of the RfCl$$_{4}$$$$cdot$$2(TOPO) complex is lower than that of the corresponding species of the homologues.

Journal Articles

Anionic fluoro complex of element 105, Db

Kasamatsu, Yoshitaka*; Toyoshima, Atsushi; Asai, Masato; Tsukada, Kazuaki; Li, Z.; Ishii, Yasuo; Tome, Hayato*; Sato, Tetsuya; Kikuchi, Takahiro; Nishinaka, Ichiro; et al.

Chemistry Letters, 38(11), p.1084 - 1085, 2009/10

 Times Cited Count:15 Percentile:48.93(Chemistry, Multidisciplinary)

We report on the characteristic anion-exchange behavior of the superheavy element dubnium (Db) with atomic number Z = 105 in HF/HNO$$_{3}$$ solution at the fluoride ion concentration [F$$^{-}$$] = 0.003 M. The result clearly demonstrates that the fluoro complex formation of Db is significantly different from that of the group-5 homologue Ta in the 6th period of the periodic table while the behavior of Db is similar to that of the lighter homologue Nb in the 5th period.

Journal Articles

Decay properties of $$^{266}$$Bh and $$^{262}$$Db produced in the $$^{248}$$Cm + $$^{23}$$Na reaction

Morita, Kosuke*; Morimoto, Koji*; Kaji, Daiya*; Haba, Hiromitsu*; Ozeki, Kazutaka*; Kudo, Yuki*; Sato, Nozomi*; Sumita, Takayuki*; Yoneda, Akira*; Ichikawa, Takatoshi*; et al.

Journal of the Physical Society of Japan, 78(6), p.064201_1 - 064201_6, 2009/06

 Times Cited Count:30 Percentile:78.34(Physics, Multidisciplinary)

Decay properties of an isotope $$^{266}$$Bh and its daughter nucleus $$^{262}$$Db produced by the $$^{248}$$Cm($$^{23}$$Na,5$$n$$) reaction were studied by using a gas-filled recoil separator coupled with a position-sensitive semiconductor detector. $$^{266}$$Bh was clearly identified from the correlation of the known nuclide, $$^{262}$$Db. The obtained decay properties of $$^{266}$$Bh and $$^{262}$$Db are consistent with those observed in the $$^{278}$$113 chain, which provided further confirmation of the discovery of $$^{278}$$113.

Journal Articles

Adsorption of Db and its homologues Nb and Ta, and the pseudo-homologue Pa on anion-exchange resin in HF solution

Tsukada, Kazuaki; Haba, Hiromitsu*; Asai, Masato; Toyoshima, Atsushi; Akiyama, Kazuhiko*; Kasamatsu, Yoshitaka; Nishinaka, Ichiro; Ichikawa, Shinichi; Yasuda, Kenichiro; Miyamoto, Yutaka; et al.

Radiochimica Acta, 97(2), p.83 - 89, 2009/02

 Times Cited Count:20 Percentile:77.78(Chemistry, Inorganic & Nuclear)

Anion-exchange chromatography of element 105, dubnium (Db), produced in the $$^{248}$$Cm($$^{19}$$F, 5n)$$^{262}$$Db reaction is investigated together with the homologues Nb and Ta, and the pseudo-homologue Pa in 13.9 M hydrofluoric acid (HF) solution. The distribution coefficient (K$$_{d}$$) of Db on an anion-exchange resin is successfully determined by running cycles of the 1702 chromatographic column separations. The result clearly indicates that the adsorption of Db on the resin is significantly different from that of the homologues and that the adsorption of anionic fluoro complexes of these elements decreases in the sequence of Ta $$approx$$ Nb $$>$$ Db $$geq$$ Pa.

Journal Articles

Fluoride complexation of element 104, rutherfordium (Rf), investigated by cation-exchange chromatography

Ishii, Yasuo; Toyoshima, Atsushi; Tsukada, Kazuaki; Asai, Masato; Tome, Hayato; Nishinaka, Ichiro; Nagame, Yuichiro; Miyashita, Sunao*; Mori, Tomotaka*; Suganuma, Hideo*; et al.

Chemistry Letters, 37(3), p.288 - 289, 2008/03

 Times Cited Count:20 Percentile:55.03(Chemistry, Multidisciplinary)

We have investigated cation-exchange behavior of Rf together with the lighter homologues of the group-4 elements Zr and Hf, and the tetravalent pseudo-homologue Th, in HF/HNO$$_{3}$$ solution using Automated Ion exchange separation apparatus coupled with the Detection system for Alpha spectroscopy (AIDA). The ${it K}$ $$_{d}$$ values of Zr, Hf, Th and Rf in HF/0.1 M HNO$$_{3}$$ were decreased with increasing the concentration of the fluoride ion [F$$^{-}$$], indicating the formation of the fluoride complexes. The sequence of the fluoride complexation strength is Zr $$sim$$ Hf $$>$$ Rf $$>$$ Th.

Journal Articles

Hexafluoro complex of rutherfordium in mixed HF/HNO$$_{3}$$ solutions

Toyoshima, Atsushi; Haba, Hiromitsu*; Tsukada, Kazuaki; Asai, Masato; Akiyama, Kazuhiko*; Goto, Shinichi*; Ishii, Yasuo; Nishinaka, Ichiro; Sato, Tetsuya; Nagame, Yuichiro; et al.

Radiochimica Acta, 96(3), p.125 - 134, 2008/03

 Times Cited Count:28 Percentile:85.1(Chemistry, Inorganic & Nuclear)

Formation of an anionic fluoride-complex of element 104, rutherfordium (Rf) produced in the $$^{248}$$Cm($$^{18}$$O,5n)$$^{261}$$Rf reaction was studied by an anion-exchange method based on an atom-at-a-time scale. It was found that the hexafluoro complex of Rf, [RfF$$_{6}$$]$$^{2-}$$, was formed in the studied fluoride ion concentrations of 0.0005 - 0.013 M. Formation of [RfF$$_{6}$$]$$^{2-}$$ was significantly different from that of the homologues Zr and Hf, [ZrF$$_{6}$$]$$^{2-}$$ and [HfF$$_{6}$$]$$^{2-}$$; the evaluated formation constant of [RfF$$_{6}$$]$$^{2-}$$ is at least one-order of magnitude smaller than those of [ZrF$$_{6}$$]$$^{2-}$$ and [HfF$$_{6}$$]$$^{2-}$$.

Journal Articles

Excitation energy dependence of fragment mass and total kinetic energy distributions in proton-induced fission of uranium isotopes

Nishinaka, Ichiro; Tanikawa, Masashi*; Goto, Shinichi*; Nishio, Katsuhisa; Asai, Masato; Tsukada, Kazuaki; Nagame, Yuichiro; Kudo, Hisaaki*

Nuclear Physics A, 805, p.434 - 436, 2008/00

The aim of this work is to study how shell effects of fissioning nuclei and fission fragments are responsible for deformation and mass division during descent from the saddle point to scission. We studied in detail excitation energy dependence of mass and total kinetic energy distributions in the fission of $$p$$ + $$^{233,238}$$U at incident beam energies of 10.0, 11.5 and 13.0 MeV. For the asymmetric mass division in the fission for both uranium isotopes, the obtained yield at $$A$$ $$simeq$$ 132 with the spherical shell of $$N$$ = 82 increases more largely with increasing excitation energy than that at $$A$$ $$simeq$$ 143 with deformed shell of $$N$$ = 86-88. The present excitation energy dependence shows the opposite trend observed in the thermal neutron induced fission and cold fission of actinides. We will discuss the shell effects on excitation energy dependence of fragment mass and total kinetic energy distributions in fission.

Journal Articles

Extraction behavior of rutherfordium into tributylphosphate from hydrochloric acid

Haba, Hiromitsu*; Tsukada, Kazuaki; Asai, Masato; Toyoshima, Atsushi; Ishii, Yasuo; Tome, Hayato; Sato, Tetsuya; Nishinaka, Ichiro; Ichikawa, Takatoshi; Ichikawa, Shinichi; et al.

Radiochimica Acta, 95(1), p.1 - 6, 2007/01

 Times Cited Count:15 Percentile:70.27(Chemistry, Inorganic & Nuclear)

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69 (Records 1-20 displayed on this page)