• The Korean Journal of Ceramics
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• v.6 no.1
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• pp.47-52
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• 2000

Lanthanides such as La, Gd and Ce have recognized as elements of high level radioactive wastes immobilized by forming solid solution with $CaTiO_3$. For easy forming solid solution between $CaTiO_3$and lanthanides, the combustion synthesis process was applied and the powder characteristics and sinterability were investigated. The proper selection of the type and the composition of fuels are important to get the crystalline solid solution of $CaTiO_3$and lanthanides. When glycine or the mixtures of urea and citric acid with stoichiometric composition was used as a fuel, the solid solution of $CaTiO_3$with $La_2O_3$or $Gd_2O_3$or $CeO_2$was produced very well by the combustion process. The combustion synthesized powder seemed to have a good sinterability with the linear shrinkage of more than 25% up to $1500^{\circ}C$, while that of the solid state reacted powder was less than 10% at the same condition.

• Journal of Radiopharmaceuticals and Molecular Probes
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• v.7 no.2
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• pp.69-77
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• 2021

No-carrier-added holmium-166 (n.c.a ¹⁶⁶Ho) separation is performed based on the results of separation conditions using stable isotopes dysprosium (Dy) and holmium (Ho) to minimize radioactive waste from separation optimization procedures. Successful separation of two adjacent lanthanides was achieved by cation-exchange chromatography using a sulfonated resin in the H+ form (BP-800) and α-hydroxyisobutyric acid (α-HIBA) as eluent. For the identification process after separation of stable isotopes, the use of chromogenic reagents alternatively enables on-line detection because the lanthanides are hardly absorb light in the UV-vis region or exhibit radioactivity. Four different chromogenic reagents were pre-tested to evaluate suitable coloring reagents, of which 4-(2-Pyridylazo)resorcinol is the most recommendable considering the sensitivity and specificity for lanthanides. Lanthanide radioisotopes (RI) were monitored for separation with an RI detector using a lab-made separation LC system. Under the proper separation conditions, the n.c.a ¹⁶⁶Ho was effectively obtained from a large amount of 100 mg dysprosium target within 2 hrs.

• Journal of the Korean Ceramic Society
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• v.43 no.11 s.294
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• pp.688-692
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• 2006

Ferroelectric lanthanides-substituted $Bi_4Ti_3O_{12}$ $(Bi_{4-x}Ln_xTi_3O_{12}, BLnT)$ thin films approximately 200 nm in thickness were deposited by metal organic chemical vapor deposition onto Pt(111)/Ti/SiO$_2$/Si(100) substrates. Many researchers reported that the lanthanides substitution for Bi in the pseudo-perovskite layer caused the distortion of TiO$_6$ octahedron in the a-b plane accompanied with a shift of the octahedron along the a-axis. In this study, the effect of lanthanides (Ln=Pr, Eu, Gd, Dy)-substitution and crystallization temperature on their ferroelectric properties of bismuth titanate $(Bi_4Ti_3O_{12}, BIT)$ thin films were investigated. As BLnT thin films were substituted to lanthanide elements (Pr, Eu, Gd, Dy) with a smaller ionic radius, the remnant polarization (2P$_r$) values had a tendency to increase and made an exception of the Eu-substituted case because $Bi_{4-x}Eu_xTi_3O_{12}$ (BET) thin films had the smaller grain sizes than the others. In this study, we confirmed that better ferroelectric properties can be expected for films composed of larger grains in bismuth layered peroskite materials. The crystallinity of the thin films was improved and the average grain size increased as the crystallization temperature,increased from 600 to 720$^{\circ}C$. Moreover, the BLnT thin film capacitor is characterized by well-saturated polarization-electric field (P-E) curves with an increase in annealing temperature. The BLnT thin films exhibited no significant degradation of switching charge for at least up to $1.0\times10^{11}$ switching cycles at a frequency of 1 MHz. From these results, we can suggest that the BLnT thin films are the suitable dielectric materials for ferroelectric random access memory applications.

• Bulletin of the Korean Chemical Society
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• v.33 no.11
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• pp.3871-3874
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• 2012

• Journal of the Korean Chemical Society
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• v.35 no.5
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• pp.520-526
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• 1991

Retention behavior of lanthanides was studied on the dynamic system using dinonylnaphthalene sulfonic acid cation exchanger and tartaric acid as a complexing agent. The relations between logk' and log$[NH^{4+}]$/log[tartarate], and between logk' and logR showed good linearity in isocratic and gradient elution, respectively. In gradient elution of tartaric acid the slopes were increased as the initial concentrations were decreased. Column efficiencies and resolution of lanthanides on dinonylnaphthalene sulfonic acid equilibrated cation exchanger were found to be better in ${\alpha}$-hydroxyisobutyric acid eluent than in tartaric acid.

• Proceedings of the Korean Nuclear Society Conference
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• 1999.10a
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• pp.304.2-304
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• 1999

• Bulletin of the Korean Chemical Society
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• v.14 no.2
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• pp.165-166
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• 1993

• Journal of the Korean Chemical Society
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• v.7 no.4
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• pp.245-250
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• 1963

Synergistic effect was observed in the extraction of trivalent lanthanides by the mixed solvent of TBPO (tri-n-butyl phosphine oxide) and TOPO (tri-n-octyl phosphine oxide) in toluene diluent. The reason of the enhancement was verified as mainly due to the formation of new extractable species $M(NO_3)_3(TBPO)_2\;(TOPO)$ besides of the formation of $M(NO_3)_3(TBPO)_3$and $M(NO_3)_3(TOPO)_3$.

• Journal of the Korean Chemical Society
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• v.34 no.3
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• pp.280-287
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• 1990

The electrochemical behavir of trivalent lanthanides [Sm(Ⅲ), Tb(Ⅲ), and Yb(Ⅲ)) complexes were investigated by the use of direct current, differential pulse polarography and cyclic voltammetry in aprotic media. These reduction peak were irreversible one-electron processes at $E_{pc}$ = -0.16 V, -0.35 V, -0.14 V, and -0.03 V of trivalent lanthanide complexes vs. Ag/AgCl electrode and the behavior of heavier lanthanides were decreased Sm > Tb > Ho > Yb order of the stability constant with decreasing atomic number.

• Proceedings of the Korean Nuclear Society Conference
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• 2001.10a
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• pp.297.1-297
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• 2001