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Journal Articles

Chemical state analysis of trace-level alkali metals sorbed in micaceous oxide by total reflection X-ray photoelectron spectroscopy

Baba, Yuji; Shimoyama, Iwao; Hirao, Norie*

Applied Surface Science, 384, p.511 - 516, 2016/10

AA2016-0127.pdf:0.71MB

 Times Cited Count:5 Percentile:25.9(Chemistry, Physical)

Chemical states of cesium as well as the other alkali metals (sodium and rubidium) sorbed in micaceous oxides have been investigated by total reflection X-ray photoelectron spectroscopy (TR-XPS). For cesium, it was shown that ultra-trace amount of cesium down to about 100 pg/cm$$^{-2}$$ can be detected by TR-XPS. This amount corresponds to about 200 Bq of $$^{137}$$Cs (t$$_{1/2}$$ = 30.2y). It was demonstrated that ultra-trace amount of cesium corresponding to radioactive cesium level can be measured by TR-XPS. As to the chemical states, it was found that core-level binding energy in TR-XPS for trace-level cesium shifted to lower-energy side compared with that for thicker layer. A reverse tendency is observed in sodium. Based on charge transfer within a simple point-charge model, it is concluded that chemical bond between alkali metal and micaceous oxide for ultra-thin layer is more polarized that for thick layer.

Journal Articles

Recovery of alkali salt by supercritical fluid leaching method using carbon dioxide

Watanabe, Takeshi*; Tsushima, Satoru*; Yamamoto, Ichiro*; Tomioka, Osamu; Meguro, Yoshihiro; Nakashima, Mikio; Wada, Ryutaro*; Nagase, Yoshiyuki*; Fukuzato, Ryuichi*

Proceedings of 2nd International Symposium on Supercritical Fluid Technology for Energy and Environment Applications (Super Green 2003), p.363 - 366, 2004/00

Recovery of salts by supercritical fluid leaching (SFL) method using carbon dioxide was experimentally studied. It was confirmed that LiCl was recovered with a mixed fluid of carbon dioxide and methanol, and KCl and SrCl$$_2$$ were recovered with a mixed fluid of carbon dioxide, methanol and crown ether. The influence of crown ether for KCl and SrCl$$_2$$ extraction were found to increase in the order of 15-crown-5 (15C5) $$<$$ 18-crown-6 (18C6) $$<$$ dicychlohexyl-18-crown-6 (DC18C6). It is expected that other salts can be recovered selectively with a mixed fluid of carbon dioxide, methanol and suitable crown ether.

Journal Articles

Development of radioactive waste treatment by Supercritical Fluid Leaching (SFL) method

Nagase, Yoshiyuki*; Masuda, Kaoru*; Wada, Ryutaro*; Yamamoto, Ichiro*; Tomioka, Osamu; Meguro, Yoshihiro; Fukuzato, Ryuichi*

Proceedings of 2nd International Symposium on Supercritical Fluid Technology for Energy and Environment Applications (Super Green 2003), p.254 - 257, 2004/00

no abstracts in English

Journal Articles

Evidence for a difference in the dissociation mechanisms of acetylene (HCCH) and vinylidene (H$$_{2}$$C=C:) from charge inversion mass spectrometry

Hayakawa, Shigeo*; Tomozawa, Koji*; takeuchi, takae*; Arakawa, Kazuo; Morishita, Norio

Physical Chemistry Chemical Physics, 5(11), p.2386 - 2390, 2003/05

 Times Cited Count:15 Percentile:44.45(Chemistry, Physical)

The process of formation of the negative ions in charge inversion mass spectrometry is via near-resonant neutralization followed by spontaneous dissociation, and then endothermic negative ion formation. The intensity of the C$$_{2}$$$$^{-}$$ peak relative to the C$$_{2}$$H$$^{-}$$ peak in these spectra increased with decreasing ionization potential of the targets for both of the isomeric C$$_{2}$$H$$_{2}$$$$^{+}$$ cations. The formation of the C$$_{2}$$$$^{-}$$ anion is proposed to result from the dissociation of excited C$$_{2}$$H$$_{2}$$ neutrals into C$$_{2}$$ and H$$_{2}$$. The dependence on target species of the intensities of C$$_{2}$$$$^{-}$$ peak relative to the C$$_{2}$$H$$^{-}$$ peak for HCCH and H$$_{2}$$C=C: cannot be rationalized by the internal energy of the excited C$$_{2}$$H$$_{2}$$ neutrals. The differences indicate that the isomeric C$$_{2}$$H$$_{2}$$ neutrals dissociate into C$$_{2}$$H and H prior to 1,2-hydrogen atom migration.

Journal Articles

A New technique to study the dissociation of energy-selected neutral intermediates

Hayakawa, Shigeo*; Harada, Kengo*; Watanabe, Nobuaki*; Arakawa, Kazuo; Morishita, Norio

International Journal of Mass Spectrometry, 202(1-3), p.A1 - A7, 2000/10

 Times Cited Count:16 Percentile:60.07(Physics, Atomic, Molecular & Chemical)

no abstracts in English

Journal Articles

Study of dissociation of neutral intermediates using charge inversion mass spectrometry

Hayakawa, Shigeo*; Harada, Kengo*; Arakawa, Kazuo; Morishita, Norio

Journal of Chemical Physics, 112(19), p.8432 - 8435, 2000/05

 Times Cited Count:19 Percentile:50.82(Chemistry, Physical)

no abstracts in English

JAEA Reports

Physico-chemical studies on the disposal of miscellaneous radioactive waste through A single-step process (III)

Iwase, Masanori*

JNC TJ8400 2000-063, 78 Pages, 2000/03

JNC-TJ8400-2000-063.pdf:1.93MB

This study is aimed at controlling oxidation reaction of molten metal by ash in incineration systems, and at positively utilizing the oxidation reaction for decontamination of slag. In this year, in order to investigate physico-chemical properties of mixed fused salt containing alkali sulfates, with special focus on the behaviour of oxygen anion in the melts, Cu$$^{2+}$$ / Cu$$^{+}$$ redox equilibrium experiments were carried out. Among the effect of various parameters on Cu$$^{2+}$$ / Cu$$^{+}$$ ratio in binary and ternary alkali sulfate melts, the effect of partial pressures of oxygen and SO$$_{2}$$ was mainly investigated in the study. Variation in Cu$$^{2+}$$ / Cu$$^{+}$$ ratio were presented as the function of partial pressures of oxygen and SO$$_{2}$$, respectively. Possible thermodynamic interpretation were made on the experimental results. In addition, the dissolution of Cr$$_{2}$$O$$_{3}$$ in mixed alkali sulfates were also investigated as a first step to elucidate the mechanism of hot corrosion. With this investigation, an important finding was obtained that the solubility of Cr$$_{2}$$O$$_{3}$$ for melts with same average ionic radius, in other words, oxygen ion activity, were essentially identical under constant temperature and atmosphere.

JAEA Reports

None

*

JNC TJ7440 99-008, 58 Pages, 1999/02

JNC-TJ7440-99-008.pdf:0.13MB

no abstracts in English

JAEA Reports

None

PNC TJ1601 98-004, 16 Pages, 1998/03

PNC-TJ1601-98-004.pdf:3.05MB

no abstracts in English

JAEA Reports

None

Wada, Yukio; Funasaka, Hideyuki; Myochin, Munetaka; Yamamoto, Kazunori; Harada, Hideo; ;

PNC TN8100 96-005, 16 Pages, 1996/01

PNC-TN8100-96-005.pdf:1.6MB

no abstracts in English

Journal Articles

Discrimination of C$$_{3}$$H$$_{4+}$$ isomeric ions by charge inversion mass spectrometry using an alkali metal target

*; *; Arakawa, Kazuo; Morishita, Norio; *

Int. J. Mass Spectrom. Ion Process, 151, p.89 - 95, 1995/00

no abstracts in English

Journal Articles

Magnetic studies on alkali metal uranates(V)MUO$$_{3}$$ with the perovskite structure

Hinatsu, Yukio

Journal of Alloys and Compounds, 203, p.251 - 257, 1994/00

 Times Cited Count:23 Percentile:81.05(Chemistry, Physical)

no abstracts in English

Journal Articles

Uranates of alkali and alkaline earth metals

Fujino, Takeo

Nihon Genshiryoku Gakkai-Shi, 20(4), p.241 - 254, 1978/04

 Times Cited Count:5

no abstracts in English

JAEA Reports

Diffusion of Alkali and Alkali Earth Metals in Various Graphites

; Iwamoto, K.

JAERI-M 5927, 22 Pages, 1974/12

JAERI-M-5927.pdf:2.33MB

no abstracts in English

Oral presentation

Elucidation for thermal decomposition behaviour of the high-level radioactive liquid waste; Effect on the thermal decomposition reaction of lanthanoid/alkali metal nitrates caused by ruthenium

Kawai, Kota*; Nakano, Yoshio*; Takeshita, Kenji*; Nagai, Takayuki; Kobayashi, Hidekazu; Amamoto, Ippei; Ayame, Yasuo

no journal, , 

no abstracts in English

Oral presentation

Chemical-state analysis of trace-level alkali metals and alkaline-earth metals sorbed in layered oxides by total-reflection X-ray photoelectron spectroscopy

Baba, Yuji; Shimoyama, Iwao; Hirao, Norie*

no journal, , 

Chemical states of trace-level alkali metals (Na, Rb, Cs) and alkaline-earth metals (Sr) adsorbed on oxides and sorbed in micaceous oxides have been investigated by X-ray photoelectron spectroscopy under X-ray total-reflection (TR) condition. Owing to the background reduction in TR-XPS spectra, we could observe down to 100 pg/cm$$^{-2}$$ for cesium and 150 pg/cm$$^{-2}$$ for strontium, respectively, sorbed in micaceous oxides. These amounts correspond to about 200 Bq of $$^{137}$$Cs (t1/2=30.2y), and 300 Bq of 90Sr (t1/2=28.8y), so it was demonstrated that trace-level cesium and strontium corresponding to radionuclide level can be measured by TR-XPS. As to the chemical states, it is concluded that the chemical bond between alkali metals and micaceous oxide for ultra-thin layer is more polarized that for thick layer on the basis of a charge transfer within a simple point-charge model.

Oral presentation

Development of analytical methods for metal elements in reprocessing solution by optical emission spectrometry based on liquid electrode plasma, 5; Determination of alkaline and alkaline earth metals in reprocessing process solution

Yamamoto, Masahiko; Do, V. K.; Taguchi, Shigeo; Takamura, Yuzuru*; Kuno, Takehiko

no journal, , 

The measurement conditions of Na, K, Ca, Sr, Ba by liquid electrode plasma optical emission spectrometry (LEP-OES) have been optimized. The samples from reprocessing process plant such as highly active liquid waste has been also measured by LEP-OES.

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