• Journal of the Korean Wood Science and Technology
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• 제15권4호
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• pp.26-31
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• 1987

맹종죽, 왕대, 솜대 Dioxane Lignin의 UV, IR spectrum의 특징(特徵)을 조사(調査)하여 본 바, 그 결과(給果)를 요약하면 다음과 같다. 1. UV spectrum에 있어서는 일반적(一般的)인 Lignin spectrum과 같이 Maximum peak, Shallow minium peak, Minimum peak의 3개소(個所)를 보였는데 Max. peak는 210nm 부근(附近), Shallow peak는 260-270nm에, Minimum peak는 280nm부근(附近)에 있었다. 2. 280nm부근(附近)의 Minimum peak는 Lignin이 갖는 특징적(特徵的)인 peak로서 일반(一般) 침엽수재(針棄樹材) Lignin이나 활엽수(闊葉樹) Lignin과는 달리 282-285nm에서 흡광도(吸光度)가 꼭 같아 아주 완만한 peak 를 보여 주었다. 3. IR spectrum에 있어서는 방향핵(芳香核) 흡수대(吸收帶)는 $1550cm^{-1}$ 부근(附近)에 있고 1040-$1130cm^{-1}$부근(附近)과 1230-$1275cm^{-1}$에서의 Spectrum 형태(形態)는 활엽수(闊葉樹)에 가깝고 침엽수재(針葉樹材) Lignin의 spectrum과는 상반되는 모습을 보여 주었다.

• 한국응용과학기술학회지
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• 제16권4호
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• pp.273-279
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• 1999

In order to study a reversible photoisomerization of disperse red l(DR 1) attached on natural polymers, cellulose acetate containing DR l(DR 1/CA adduct) was prepared, and the changes of UV/VIS spectra of its solution(benzene, DMAc). thick film, and LB film were investigated by alternate irradiation with two different wave length lights. DR 1/CA adduct was prepared through tosylation of partially hydrolyzed cellulose acetate followed by reaction with DR 1 at $100^{\circ}C$ in pyridine. From the UV/VIS spectra of DR 1/CA adduct dissolved in DMAc solvent including phosphoglyceride before and after irradiation at 360nm and 45Onm, we found out the changes of UV/VIS spectra were reversible. In addition, the change of UV/VIS spectra of this adduct solution was strongly depended on the sorts of solvents and temperature. As the temperature was increased, UV/VIS spectra of this adduct solution in DMF showed blue shift. These results provided this solution could be applied to a temperature sensor. In the thick film case, we also obtained similar results with solution case. LB monolayer and trilayer from DR 1/CA adduct was obtained by scattering the solution including phosphoglyceride on water surface at the surface pressure of 8mN/m. After irradiation on that LB monolayer and trilayer, the reversible photoisomerization was also detected. From these results we concluded DR 1/CA adduct was suitable for the application to data storage and optical switch, etc.

• 한국환경과학회지
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• 제18권6호
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• pp.667-674
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• 2009

This study has carried out to evaluate the effect of NaCI as electrolyte of single (electrolysis and UV process) and complex (electrolysis/UV) processes for the purpose of removal and mineralization of Rhodamine B (RhB) dye in water. It also evaluated the synergetic effect on the combination of electrolysis and UV process. The experimental results showed that RhB removal of UV process was decreased with increase of NaCl, while RhB removal of electrolysis and electrolysis/UV process was increased with increase of NaCI. The decolorization rate of the RhB solution in every process was more rapid than the mineralization rate identified by COD removal. The latter took longer time for further oxidation. Absorption spectra of an aqueous solution containing RhB showed a continued diminution of the RhB concentration in the bulk solution: concomitantly, no new absorption peaks appeared. This confirmed the decolorization of RhB, i.e., the breakup of the chromophores. It was observed that RhB removal in electrolysis/UV process is similar to the sum of the UV and electrolysis. However, it was found that the COD of RhB could be degraded more efficiently by the electrolysis/UV process than the sum of the two individual process. A synergetic effect was demonstrated in electrolysis/UV process.

• Bulletin of the Korean Chemical Society
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• 제35권2호
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• pp.531-538
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• 2014

The quantum mechanical properties of a series of oligo-para-phenylenes (2-11) were characterized using DFT B3LYP/6-311G(d,p) calculations. The global minimum among the various torsional conformers of an oligo-p-phenylene is calculated to be a twist conformation. A less stable planar conformation, in which all the dihedral angles in oligo-p-phenylene are restricted to be planar, has also been calculated. The total electronic energies, normal vibrational modes, Gibbs free energies, and HOMOs and LUMOs of the two different conformations (twisted and planar) of the oligo-p-phenylenes were analyzed. The energy differences between the HOMOs and LUMOs of the substrates are in accord with the maximum absorption peaks of the experimental UV spectra of 2-6. The calculated normal vibrational modes of 2-6 were comparable with their experimental IR spectra.

• Fibers and Polymers
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• 제6권2호
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• pp.127-130
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• 2005

Intrinsic UV reflection and fluorescence behaviors of polycarbonate, polyurethane and poly(ethylene terephthalate) films were investigated in order to characterize the interaction of water in these films. During water sorption process, UV reflection spectra of polycarbonate and polyurethane films showed little peak position changes. Fluorescence emission spectra of polycarbonate films showed red spectral shifts from 332 nm with water immersion time. This red-shifted peak could be due to phenyl-2-phenoxybenzoate, which is one of the major thermal degradation products in polycarbonate. Fluorescence peaks of polyurethane films appeared at two different positions and the ratio of these peak intensities increased with increasing immersion time. In the case of PET films, the UV reflection spectrum showed the peak intensity around 340 nm to change in response to water sorption. The fluorescence near 388 nm probably due to ground state dimer exhibited sensitivity with water sorption, when excited at 340 nm.

• Macromolecular Research
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• 제12권1호
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• pp.22-25
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• 2004

We have synthesized aniline oligomer composites by using heteropoly acid (H$_4$SiW$_{12}$O$_{40}$ ) as a dopant. The doping and dedoping processes of the aniline oligomer composites were investigated with the aid of UV- Vis spectra. The bands of the aniline oligomer at 572 nm weakened or disappeared, and the bands at 268, 412, and 771 nm appeared, after the aniline oligomer was doped. When the solution of the aniline oligomer doped with H$_4$SiW$_{12}$O$_{40}$ was kept at lower values of pH, the aniline oligomer could not be dedoped by dilution. The turning point of doping and dedoping occurred at pH 5.5. The band at 771 nm shifted towards longer wavelengths when the aniline oligomer composites were synthesized using acetone as the solvent. This observation indicates that the molecular chain became stretched. In addition, we also investigated the change of the electronic absorption spectra of the composites with respect to the time laid up.id up.

• 약학회지
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• 제35권1호
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• pp.1-6
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• 1991

Fast Hartley transform(FHT) was used for the identification of derivative UV spectra of pharmaceuticals, with the advantages of relatively shorter computing time of FHT and more precise results. The arccosine value of dot product of two vectors of normalized FHT coefficients calculated from two compared derivative spectra was a reasonable parameter for the spectral identification. Using this parameter, the similar patterns of derivative spectra of 13 penicillins can be differenciated from each other. The concentration difference and the minor contamination did not interfere the results of identification procedures. All these procedures of identification were accomplished successfully by the computer program, [SPECMAN PLUS] version 1.30, which was developed for this article.

• 대한화학회지
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• 제13권1호
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• pp.25-28
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• 1969

몇가지 monoazo 一金屬錯鹽들의 UV吸收 spectra를 測定하여 이것을 基礎로 하여 그 金屬錯鹽들의 構造를 論하였다. 옆으로 찌그러진 八面體모양의 幾何學的構造를 提案하였다.

• Bulletin of the Korean Chemical Society
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• 제23권9호
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• pp.1315-1327
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• 2002

The model compounds, 8-methoxypsoralen-CH2O(CH2)n-adenine (MOPCH2OCnAd, n=2, 3, 5, 6, 8, and 10) in which 5 position of 8-methoxypsoralen (8-MOP) is linked by various lengths of polymethylene bridge to N9 of adenine. UV absorption spectra are identical with the sum of MOPCH2OC3 and adenine absorption spectra. Solvent effects on the UV absorption and fluorescence emission spectra indicate that the lowest excited singlet state is the $(\pi${\rightarrow}$\pi*)$ state. The spectral characteristics of the fluorescence of MOPCH2OCnAd are strongly dependent upon the nature of the solvents. The fluorescence emission spectra in aprotic solvents are broad and structureless due to the excimer formation through the folded conformation accelerated by hydrophobic ${\pi}-{\pi}$ stacking interaction. Increasing polarity of the protic solvents leads to higher population of unfolded conformation stabilized through favorable solvation and H-bonding, and consequently to an increase in the fluorescence intensity, fluorescence lifetime, and a shift of fluorescence maximum to longer wavelengths. The decay characteristics of the fluorescence in polar protic solvents shows two exponential decays with the lifetimes of 0.6-0.8 and 1.6-1.9 ns in 5% ethanol/water, while MOPCH2OC3 shows 0.5 and 1.7 ns fluorescence lifetimes. The long-lived component of fluorescence can be attributed to the relaxed species (i.e., the species for which the solvent reorientation (or relaxation) has occurred), while the short-lived components can be associated with the unrelaxed, or only partially relaxed, species.

• Journal of the Korean Wood Science and Technology
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• 제12권3호
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• pp.35-40
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• 1984

지리산산(智異山産) 침엽수재(針葉樹材) 10개(個) 수종(樹種)에 대(對)한 AcBr lignin의 UV spectrum을 조사(調査)하여 본 바 각(各) 수종(樹種) 모두 spectrum curve의 정점(頂點)은 249nm(Max. peak), 267-268nm(Shallow min. peak), 280nm(Lower max. peak)에 있었으며 Bjorkman lignin이나 lignin sulfonic acid 등(等)의 UV spectrum 상(上)에서 볼 수 있는 견(肩)은 AcBr lignin의 spectrum curve 상(上)에서는 볼 수 없었으며 각(各) 정점(頂點)의 10개(個) 수종(樹種) 평균(平均) 흡광도(吸光度)와 흡광계수(吸光係數)는 249nm에 각각(各各) $0.367{\pm}0.0015$, $24.56{\pm}0.0535$, 267-268nm에서 $0.278{\pm}0.0016$, $18.50{\pm}0.0569$ 였고 280nm에서는 $0.306{\pm}0.0016$, $20.42{\pm}0.0627$ 이었다.