• Transactions on Electrical and Electronic Materials
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• v.18 no.6
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• pp.323-329
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• 2017

This reports the electrical behavior, bonding structure and Schottky contact of gallium-zinc-oxide (GZO) thin film annealed at $100{\sim}400^{\circ}C$. The mobility of GZO with high density of PL spectra and crystal structure was also increased because of the structural matching between GZO and Si substrate of a crystal structure. However, the GZO annealed at $200^{\circ}C$ with an amorphous structure had the highest mobility as a result of a band to band tunneling effect. The mobility of GZO treated at low annealing temperatures under $200^{\circ}C$ increased at the GZO with an amorphous structure, but that at high temperatures over $200^{\circ}C$ also increased when it was the GZO of a crystal structure. The mobility of GZO with a Schottky barrier (SB) was mostly increased because of the effect of surface currents as well as the additional internal potential difference.

• Journal of Advanced Marine Engineering and Technology
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• v.23 no.4
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• pp.514-522
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• 1999

The laser-induced plasma affects greatly on the results of welding process. moreover selective evaporation loss of alloying elements leads to change in chemical composition of weld metal as well as the mechanical properties of welded joint. this study was undertaken to obtain a fundamental knowledge of pulsed laser welding phenomena especially evaporation mechanism of different aluminum alloys. The intensities of molecular spectra of AlO and MgO were different each other depeding on the power density of a laser beam Under the low power density condition the MgO band spectrum was predominant in intensity while the AlO spectra became much stronger with an increase in the power density. These behaviors have been attributed to the difference in evaporation phenomena of Al and Mg metals with different boiling points and latent heats of vaporization. The time-averaged plasma temperature and electron number density were determined by spectroscopic methods and consequently the obtained temperature was $3,280{\pm}150K$ and the electron number density was $1.85{\times}10^{19}\;l/m^3$.

• Bulletin of the Korean Chemical Society
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• v.22 no.8
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• pp.833-836
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• 2001

Infrared absorption spectra of $\alpha\omega-diphenylpolyenyl$, anions Ph(CH)nPh- (DPn-, n=7, 9, and 13) in the tetrahydrofuran-d6 solutions was measured in the range of 1700 and 1200 cm-1 . The infrared spectra obtained from anions (DPn) showed considerable difference from their neutral species (DPn); their intensities were enhanced at least two orders of magnitude stronger than their neutral species. The in-plane CH bending modes at 1464 and 1375 cm-1 are correspondingly strengthened with the chain length increased, but the C=C stretching at 1541 cm-1 is weakened and frequencies are not changed. We provide an IR evidence for the first time that the bond order or bond alternations of the anions (soliton) are different from those of radical anions (polaron) as well as neutral species.

• Bulletin of the Korean Chemical Society
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• v.13 no.5
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• pp.520-526
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• 1992

The intramolecular fundamental vibrations of $CH_3CN$ trapped in solid argon matrix have been reinvestigated by means of FT-IR spectroscopy in the spectral range of 4000-500 $cm^{-1}$. By employing a quantum detector, infrared spectra could be obtained at matrix to solute ratio of 10000, allowing the clarification of the peaks due to monomeric species more clearly. Temperature controlled diffusion was initiated to identify the dimeric and polymeric species in terms of difference spectra. The assignments of monomeric and dimeric species are found, in general, to agree with the earlier work performed at higher concentration (Ar/$CH_3CN$ = 1500) using a dispersive spectrometer. Nonetheless the difficulty of minute differences between the earlier infrared and Raman spectroscopic results could be resolved. Moreover, the previously unnotified peaks due to polymeric species have been identified.

• Proceedings of the Korean Nuclear Society Conference
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• 1997.05b
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• pp.477-482
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• 1997

Safe shutdown earthquakes (SSE) of four existing nuclear power plant sites were evaluated by using a probabilistic method. It turned out that the SSE's of the two sites are smaller than those of the rest. Site-specific response spectra were developed for two sites of which SSE's show a comparatively large difference. The result shows that the site-specific response spectrum of one site is higher by a factor of 1.5 than that of the other. The comparison of uniform hazard spectrum and site-specific response spectrum at one of the two sites shows that the both spectra are consistent with each other.

• Journal of Photoscience
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• v.9 no.2
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• pp.126-129
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• 2002

The chromophore/protein interactions in the photocycle intermediates of photoactive yel- low protein (PYP) were probed by site-directed mutagenesis. The absorption spectra of L- intermediates produced from E46Q, T50V, and R52Q mutants were calculated using the absorption spectra of dark states and difference absorption spectra between L-intermediates and dark states, and compared with that of PYP$\_$L/. The absorption spectrum of R52Q$\_$L/ agreed with that of PYP$\_$L/, but those of E46Q$\_$L/ and T50V$\_$L/ were red-shifted. The effect of these mutations on the absorption spectrum for L-intermediate was comparable to that for the dark state, suggesting that the interaction around the phe-nolic oxygen of the chromophore is conserved in PYP$\_$L/ unlike the crystal structure. On the other hand, we have reported that the absorption spectra of Y 42F$\_$M/, T50V $\_$M/, and R52Q$\_$M/ agreed with that of PYP$\_$M/, but that of E46Q$\_$M/ was red-shifted, suggesting that the hydrogen bond of the chromophore with Glu46 is conserved but that with Tyr42 is broken in PYP$\_$M/. These results suggest that the chromophore inter-acts with Glu46 throughout the photocycle, but never directly interacts with Arg52. This model con- flicts with some of the structural model of PYP intermediates proposed based on the high-resolution X -ray crystallography.

• YAKHAK HOEJI
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• v.55 no.3
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• pp.260-266
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• 2011

Two types of water soluble lysine salts of ibuprofen were prepared and evaluated. Physicochemical properties for ibuprofen-l-lysinate (IBL-l), ibuprofen-dl-lysinate (IBL-dl) and ibuprofen (IB) were studied on melting point, specific ratation, UV spectra and $^1H$-NMR spectra. There were not differences between IBL-dl and IBL-l in UV spectra and $^1H$-NMR spectra. The pharmacokinetic parameters of IB were compared to those of its lysine salts (IBL-l and IBL-dl) after i.v. or oral administration at the dose of 50 mg/kg (calculated as IB). Total body clearance ($CL_t$) and area under the plasma concentration-time curve (AUC) were not different between IB group and IBL groups after i.v. administration. On the other hand, IBL-l and IBL-dl produced peak plasma concentrations ($C_{max}$) significantly ealier and higher than IB. Time to reach peak concentration ($T_{max}$) after IBL administration was lower than that after IB administration. There was no difference in AUC across all different groups (IB, IBL-l and IBL-dl) after oral administration. However, absorption rate constant ($k_a$) of IBL-l and IBL-dl were significantly increased than that of IB. These results indicated that the administration of IBL-l and IBL-dl may be advantageous if rapid and reliable onset of pain relief is required.

• Bulletin of the Korean Chemical Society
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• v.19 no.9
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• pp.934-942
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• 1998

$^13CO$ chemisorbed on platinum particles in L-zeolite has been investigated by static and magic angle spinning NMR spectroscopy. The representative spectra are composed of a broad asymmetric peak with a center of gravity at 230±30 ppm and a sharp symmetric peak at 124±2 ppm which is tentatively assigned to physisorbed $CO_2$, on inner walls of L-zeolite. Overall, the broad resonance component is similar to our previous results of highly dispersed (80-96%) CO/Pt/silica or CO/Pt/alumina samples, still showing metallic characters. The principal difference is in the first moment value. The broad peak in the spectra is assigned to CO linearly bound to Pt particles in the L-zeolites, and indicates a distribution of isotropic shifts from bonding site to bonding site. The NMR results reported here manifest that the Pt particles inside of the L-zeolites channels are not collectively the same with the ones supported on silica or alumina with similar dispersion in terms of Pt particle shape and/or ordering of Pt atoms in a particle. As a result, Pt particles of CO/Pt/L-zeolite were agglomerated accompanying CO desorption upon annealing. There were no definite changes in the NMR spectra due to differences of exchanged cations. Comparison of our observation on CO/Pt/L-zeolite with Sharma et al.'s reveals that even when the first moment, the linewidtb, and the relaxation times of the static spectra and the dispersion measured by chemisorption are similar, the properties of Pt particles can be dramatically different. Therefore, it is essential to take advantage of the strengths of several techniques together in order to interpret data reliably, especially for the highly dispersed samples.

• Journal of Radiation Industry
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• v.11 no.3
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• pp.157-165
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• 2017

In this paper, we calculate the light photons collection efficiency of large-volume plastic scintillation detector mainly used for radiation portal monitor (RPM). A Monte Carlo light photon transport code, DETECT2000, were used to quantitatively evaluate light collection efficiency of plastic scintillation detector. DETECT2000 calculated the placement of light collection efficiency based on the energy spectrum. We calculated the light collection efficiency relative to the position of the energy spectrum that proportional to the placement of the source. The $850{\times}285{\times}65mm^3$ size of polyvinyl toluene (PVT) scintillator was used for measurements. Through DETECT2000 simulation, the light collection efficiency of $5{\times}5$ arrays were calculated and verification was performed by comparing with experimentally measured. And then, the corrected MCNP simulation by applying the light collection efficiency in $21{\times}13$ arrays was compared and analyzed. Comparing the Monte Carlo simulation with measured results, it shows an average difference of 10.1% in $5{\times}5$ arrays. Particularly, about twice of the difference was found in the edge of first column, which coupled with PMT. In whole $5{\times}5$ array, the overall ratio was the same except for the first column. And then comparing the energy spectra of the $21{\times}13$ array with and without the light collection efficiency, it shows a difference of 6.69% in Compton edge area. The DETECT2000 based light collection efficiency simulation showed well agreement with the point source experiment. And comparing with measured energy spectra, we could compare the differences according to whether or not the light collection efficiency was applied. As a results, it is possible to increase the accuracy and reliability of Monte Carlo simulation results by pre-calculating the light collection efficiency according to the PVT geometry by using the DETECT2000.

• The Transactions of the Korean Institute of Electrical Engineers D
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• v.50 no.12
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• pp.590-596
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• 2001

The pre-emphasis is an essential process for speech signal processing. Widely used two methods are the typical method using a fixed value near unity and te optimal method using the autocorrelation ratio of the signal. This study proposes a new pre-emphasis method using the short-term energy difference of speech signal, which can effectively compensate the glottal source characteristics and lip radiation characteristics. Using the proposed pre-emphasis, speech analysis, such as spectrum estimation, formant detection, is performed and the results are compared with those of the conventional two pre-emphasis methods. The speech analysis with 5 single vowels showed that the proposed method enhanced the spectral shapes and gave nearly constant formant frequencies and could escape the overlapping of adjacent two formants. comparison with FFT spectra had verified the above results and showed the accuracy of the proposed method. The computational complexity of the proposed method reduced to about 50% of the optimal method.