• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
• /
• 2007.11a
• /
• pp.105-106
• /
• 2007

M-DNAs based on zinc and cobalt ions were formed at the conditions of $26^{\circ}C$, 76% humidity, atmosphere, and pH 8.0. Some process parameters in synthesis of M-DNA such as synthetic temperature, concentration of metal ions, and synthetic time were varied and the electrical properties were investigated by changes of the parameters. The electrical properties of M-DNA showed the dependences on synthetic temperature, concentration of metal ions and synthetic time. The I-V characteristics rapidly increased with each increase of the parameters.

• Bulletin of the Korean Chemical Society
• /
• v.2 no.1
• /
• pp.1-8
• /
• 1981

Electrochemical reduction of nitrobenzene and substituted nitrobenzenes on lead electrode was studied by galvano-static measurements and cyclic voltammetry in basic ethanol-water solvents. Nitroso compounds or hydroxylamines were detected as the main reduction product depending on the potential. Mechanisms of production and further reduction of substituted and unsubstituted nitrosobenzenes are deduced from Tafel slope, pH dependence and reaction order. The reduction of most of the substituted nitrobenzenes to corresponding nitrosobenzene derivatives seemed to follow the reaction mechanism of nitrobenzene reduction with a few exceptions. A Hammett type relationship between the magnitude of the reduction current and the kinds of substituents was found with the ${\rho}$ value of 0.54.

• Bulletin of the Korean Chemical Society
• /
• v.13 no.1
• /
• pp.37-41
• /
• 1992

The reactions of nitrous acid with hydrogen peroxide in acidic aqueous solution in the presence of several added anions have been studied at $0^{\circ}C$ and pH 2-4 to investigate the nucleophilic catalysis of these anions. From the dependence of reaction rates on the anion concentrations, significant catalytic effects were found for $Cl^-,\;Br^-,\;SCN^-$, in order of effect $SCN^-\;{\approx}\;Br^->Cl^-$, while no observable effect was found for ${ClO_4}^-$ and ${NO_3}^-$. These results support O-nitrosation reaction is the rate-determining step and NOX formed in the presence of an anion ($X^-$) also acts as a nitrosating agent and accelerates the overall reaction rate. The order of reactivity was found to be NOCl>NOBr>NOSCN, which is consistent with the results of N-nitrosation and S-nitrosation reactions.

• Bulletin of the Korean Chemical Society
• /
• v.15 no.9
• /
• pp.782-785
• /
• 1994

The dissociation kinetics of linear polyaminopolycarboxylate complexes of lanthanide ions (L$n^{3+}: Ce^{3+},\;Eu^{3+}\;and\;Yb^{3+}$) has been studied in an aqueous solution of 0.10 M (NaCl$O_4$) at 25.0${\pm}0.1^{\circ}C$ using Cu(II) ions as a scavenger. The dissociation rates of acid-catalyzed pathway decrease in the order Ln(EPDTA$)^- > Ln(DPOT)^- > In(TMDTA)^- > Ln(MPDTA)^- > Ln(EDTA)^- > Ln(PDTA)^- > Ln(DCTA)^-$ according to the present and literature data. An increase in the N-Ln-N chelate ring from 5 to 6 and substitution of two methyl groups, one ethyl and hydroxyl group on a chelate ring carbon of these ligands leads to a decrease in kinetic stabilities of the complexes. The substitution of one methyl group and cyclohexyl ring on a ring carbon, however, results in a significant increase in the kinetic stability of the resulting $Ln^{3+}$ complexes. Individual reaction steps taking place for each system, with different copper, acetate buffer concentration and pH dependence, are also discussed.

• Bulletin of the Korean Chemical Society
• /
• v.6 no.4
• /
• pp.230-233
• /
• 1985

Kinetic data of the Zn(Ⅱ) ion-catalyzed hydrolysis of 2-acetylpyridineketoximyl acetate (S) are measured. The reaction proceeds through the accumulation of an intermediate (I). 2-Acetylpyridineketoxime (Ox) is released in the breakdown step of I. Phenol is not formed as a part of the products, and, therefore, diphenyl phosphate and Ox are produced by the breakdown of I. Based on the dependence of the rates for the formation and the breakdown of I on [Zn(Ⅱ)] and pH, and considering the UV spectral properties of I, the structure of I is tentatively assigned as the penta-covalent intermediate formed by the addition of a water molecule to S.

• Bulletin of the Korean Chemical Society
• /
• v.8 no.5
• /
• pp.366-372
• /
• 1987

Cryptand[2,2] was grafted to low crosslinked styrene-divinylbenzene copolymer by substitution reaction with chloromethylated styrene-divinylbenzene copolymer. This resin was stable in concentrated acid and base, and showed a good resistance to heat. The pH, time, and concentration dependence of the adsorption of metal ions by this resin were studied. Studies on the chromatographic separation of lanthanides, $Cu^{2+}$ and $UO_2^{2+_2}$ were also carried out with various eluents. These studies demonstrate that this resin has the applicability to the preconcentration and separation of metal ions.

• Journal of Korean Vacuum Science & Technology
• /
• v.3 no.2
• /
• pp.116-120
• /
• 1999

Possible role of hydrogen atoms on the formation of microcrystalline silicon films was schematically investigated using a plasma enhanced chemical vapor deposition system. A layer-by-layer technique that can alternate deposition of ${\alpha}$-Si thin film and then exposure of H2 plasma was used for this end. The experimental process was extensively carried out under different hydrogen plasma times (t2) at a fixed number of 20 cycles in the deposition. structural properties, such as crystalline volume fractions and grain shapes were analyzed by using a Raman spectroscopy and a scanning electron microscopy. Electrical transports were characterized by the temperature dependence of the dark conductivity that gives rise to the calculation of activation energy (Ea). Optical absorption was measured using an ultra violet spectrophotometer, resulting in the optical energy gap (Eopt). Our experimental results indicate that both of the hydrogen etching and the structural relaxation effects on the film surface seem to be responsible for the growth mechanism of the crystallites in the ${\mu}$c-si films.

• Journal of Korean Vacuum Science & Technology
• /
• v.5 no.2
• /
• pp.43-46
• /
• 2001

Fe-Au alloys are characterized by the complete solubility, and exhibit an fcc-bcc structural transformation at the Fe-rich side. The magneto-optical(equatorial Ken effect : EKE) and optical properties of Fe$\_$1-x/Aux (0 < x < 1) were investigated in the 0.5 - 5.0 eV energy range. The x-ray diffraction study shows the structural fcc-bcc transformation about 80 at. % of Fe. Noticeable changes in the optical properties caused by the fcc-bcc structural transformation was observed. The shape and intensity of the EKE spectra as well as the field dependence of the magneto-optical response were also significantly changed. It is thought that these changes are mainly comes from the induced magnetic moment in Au(and/or the emhanced magnetic moment of Fe). The nature of the prominent structure observed in the UV range of the magneto-optical Ken effect of Au/Fe multilayered films are disscussed in connection with the above results.

• Journal of Korean Vacuum Science & Technology
• /
• v.7 no.1
• /
• pp.13-17
• /
• 2003

The influence of structural transition on the resistance and impedance behavior of Ni$_2$MnGa alloy was investigated. The temperature-dependent resistance and impedance were measured in a temperature range of 4 - 350 K and 185 - 300 K, respectively. The dependence of temperature coefficient of resistivity on temperature shows a kink at 220 K, which is related to the structural transition. The change in dominant scattering mechanism results in the observed kink. Significant increases were also observed around the transition temperature for both real and imaginary parts of impedance. It is thought that this phenomenon originates from disappearance of the martensite twin boundaries during the structural transformation.

• Journal of the Korean Society of Food Science and Nutrition
• /
• v.18 no.4
• /
• pp.410-422
• /
• 1989

Soybean protein isolates were acylated with succinic anhydride and partially hydrolyzed with trypsin. Chemical modification decreased protein contents of samples and, in amino acid composition, tyrosine was increased comparatively. And lysine was increased remarkably by partial proteolysis. Succinylation and trypsin treatment increased the aqueous solubility and shifted the isoelectric potint that showed high pH-dependence of protein solubility. Protein solubility was influenced by salt concentration such as $NaCl,\;CaCl_2,\;NaNO_3$ and $NaH_2PO_4$. Chemical modification increased the absorption of oil and water, emulsification properties and foam capacity, but decreased foam stability, ultraviolet absorbance and bulk density. Protein-protein Interaction between soybean protein isolates and beef protein increased the emulsifying activity, emulsifying activity index and foaming properties, but it didn't have any influence on emulsion stability.