• Journal of the Korean Chemical Society
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• v.41 no.11
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• pp.581-585
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• 1997

The luminescence spectra of Tb(Ⅲ) complexes have been investigated as a function of molar metal-to-ligand ratio and pH. The ligands used in this study are iminodiacetate (IDA) and methyliminodiacetate (MIDA). The 549 nm emission band, most sensitive to the coordination environment among the observed bands, is monitored to reveal the optimum condition for $TbL^{3-}_3$ complex formation in aqueous state.

• Bulletin of the Korean Chemical Society
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• v.6 no.1
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• pp.33-36
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• 1985

The luminescence intensity of $Tb^{3+}$ bound to picolinic acid, squaric acid, and 2,3-pyrazinedicarboxylic acid has been studied in water and water-ethanol mixtures. It has been found that the emission intensity of $Tb^{3+}$ in the complexes is enhanced with the increase of ethanol content in water-ethanol mixtures. Several factors affecting on the emission intensity of $Tb^{3+}$ in waterethanol mixtures are discussed.

• Journal of the Korean Chemical Society
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• v.27 no.1
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• pp.18-23
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• 1983

To understand the abnormal absorption behavior of rare earths in cation exchange resins, the absorption for Ce(III), Tb(III) and $Cl^-$ ions in Dowex 50W-X2 have been investigated by spectrophotometry in the concentration range of $1{\sim}12$ M HCI and $HCl-HClO_4$ mixed solutions. The amount of $Cl^-$ ion absorbed shows that the ratio of amount of $Cl^-$ ions to that of rare earths does not exceed 10% in the concentration range of $6{\sim}8M$ HCl and decreased gradually to 3% at 2M HCl and 6% at 12M HCl. The ratio is further decreased with the fraction of $HClO_4$ in $HCl-HClO_4$ mixed solutions and the decrease is presumably due to the weak tendency to form a complex between rare earths and $Cl^-$ ions in a cation exchange resin. The effect of $ClO_4^-$ is expected to play a more important role than that of $Cl^-$ ions in the large absorption of rare earths.

• Proceedings of the Korea Crystallographic Association Conference
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• 2001.05a
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• pp.17-17
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• 2001

• Proceedings of the Korean Radioactive Waste Society Conference
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• 2011.10a
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• pp.219-220
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• 2011

• Analytical Science and Technology
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• v.10 no.4
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• pp.274-281
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• 1997

Methods to determine terbium(III) ion in aqueous solution by measuring the enhanced fluorescence intensity of terbium(III)-terephthalic acid(TPA) complex ion have been studied. The optimum analytical conditions for pH, excitation wavelength and concentration of TPA were found to be 6.0, 260nm and $4.0{\times}10^{-4}M$, respectively. The fluorescence intensity of the terbium(III) complex ion was further increased with addition of trioctylphosphine oxide (TOPO). In this case Triton X-100 was used to dissolve TOPO in aqueous solution. When TOPO was used, the optimum analytical conditions for pH, excitation wavelength, and concentrations of TPA, TOPO and Triton X-100 were found to be 4.5, 285nm. $4.0{\times}10^{-4}M$, $5.0{\times}10^{-5}M$, and 0.05%, respectively. Under the optimum experimental conditions, calibration curve for Tb(III) was linear over the range from $4.0{\times}10^{-8}M$ to $4.0{\times}10^{-5}M$ and the detection limit was $4.0{\times}10^{-8}M$. When TOPO was used, the concentration range of linear response, and the detection limit were $4.0{\times}10^{-9}M$ to $2.0{\times}10^{-6}M$, and $4.0{\times}10^{-9}M$, respectively. Effects of interferences from various cations for the determination of terbium(III) ion were also investigated.

• The Bulletin of The Korean Astronomical Society
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• v.39 no.1
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• pp.32.2-32.2
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• 2014

We present a prediction for 21cm differential brightness temperature (dTb) from a set of strongly clustered sources of Population III and II objects at high redshift, from a suite of numerical simulations of their formation and radiative processes. These objects are located inside a highly biased density environment ("Rarepeak"), which is a rare, high-density peak which extends to ~7 comoving Mpcs. We study the impact on the resulting 21 cm signal from their ultraviolet and X-ray properties. The boost of emission (dTb>0) by high-density environment, moderate leakage of X-ray photons, and strong absorption due to Lyman-alpha pumping contrive to make Rarepeak a discernible, spatially-extended (sky angle~10') object around z~15, which is found to be detectable as a single object by Square Kilometre Array (SKA) with integration time of ~[600-2000] hours. We also examine detectability of many such peaks through SKA precursors.

• Proceedings of the Korean Radioactive Waste Society Conference
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• 2010.05a
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• pp.217-218
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• 2010

• Journal of the Korean Chemical Society
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• v.55 no.4
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• pp.594-602
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• 2011

The effect of ${\alpha}$-, ${\beta}$- and ${\gamma}$-picolines on the stereochemistry of the coordination compounds of lanthanide(III) nitrates derived from 4[N-(furfural)amino]antipyrine semicarbazone (FFAAPS) has been studied. The general composition of the present coordination compounds is [Ln(FFAAPS)$(NO_3)_3$Pic] (Ln=La, Pr, Nd, Sm, Gd, Tb, Dy or Ho and Pic=${\alpha}$-, ${\beta}$- or ${\gamma}$-picolines). All these coordination compounds have been characterized by elemental analyses, molecular weight, molar conductance, magnetic susceptibility, infrared and electronic spectra. The infrared studies suggest that the FFAAPS behaves as a neutral tridentate ligand with N, N, O donor while ${\alpha}$-, ${\beta}$- or ${\gamma}$-picoline is coordinated to the lanthanide(III) ions via heterocyclic N-atom. Nitrates are bicovalently bonded in these compounds. From the electronic spectral data, nephelauxetic effect (${\beta}$), covalence factor ($b^{1/2}$), Sinha parameter (${\delta}%$) and the covalence angular overlap parameter (${\eta}$) have been calculated. Thermal stabilities of these complexes have been studied by thermogravimetric analysis. The coordination number of lanthanide(III) ions in the present compound is found to be ten. The antibacterial studies screening of the primary ligand FFAAPS and the complexes showed that the present complexes have moderate antibacterial activities.

• Microbiology and Biotechnology Letters
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• v.22 no.6
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• pp.593-598
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• 1994

A bacterium KL-57 which exhibited biosurfactant activity was isolated. This bacterium was identified as Bacillus subtilis. The biosurfactant-producing gene of B. subtilis KL-57 was cloned into R subtilis MI113 by using plasmid pTB523. The plasmid DNA from the clone was found to carry a 18 kb PstI insert. The biosurfactant-producing gene was cleaved into 4 fragments by SmaI, 3 fragments by PvulI or EcoRl, 4 fragments by PvulI and EcoRI double digestion, 5 fragments by AccI, and 2 fragments by KpnI, HindIII or BamHI. By subcloning the 18 kb Pstl insert, a 2.3 kb EcoRl fragment conferred the biosurfactant producing activity on B. subtilis cells. The 2.3 kb had one HindIII cleave site. But Two fragments, which corresponds HindIII/EcoRl termini, exhibited no biosurfactant activity.