• Journal of the Korean Wood Science and Technology
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• v.28 no.1
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• pp.36-41
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• 2000

This study was carried out to introduce functional groups onto wood by reacting with 2-methacryloyloxyethyl isocyanate(MOI). The effects of the catalyst and the reaction conditions(temperature and time) on the treatment were investigated. The evidence of bonding between wood and MOI were examined by infrared(IR) spectroscopy. The change in surface characteristics of MOI treated wood was examined by water contact angle measurement and X-ray photoelectron spectroscopy(XPS). Wood reacted quickly with MOI in the presence of di-n-butiltin dilaurate catalyst. Especially, the increase in weight percent gain(WPG) with increasing in reaction time was remarkable at the reaction temperature of over $50^{\circ}C$. The IR spectrum of wood reacted with MOI showed a strong urethane absorption(1715 $cm^{-1}$) but no isocyanate(2235 $cm^{-1}$) absorption. It also showed a sharp olefinic C=C double bond absorption at 1635 $cm^{-1}$. This means that an introduced methacrylate group becomes the starting point of further graft copolymerization with another vinyl monomers. The wood modified with MOI showed a gradual increase in contact angle with increasing in WPG, which means that the hydrophilic wood surface become quite hydrophobic. Also, it was cleared that most parts of the wood surface were modified with MOI by XPS analysis.

• Polymer(Korea)
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• v.30 no.5
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• pp.373-379
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• 2006

Polymerizable discotic liquid crystals containing diacetylene and acryloyl groups were formed through hydrogen bonding between phloroglucinol core and polymerizable pyridine derivatives, and their photopolymerization behavior was investigated. The discotic complexes exhibited discotic columnar and rectangular columnar mesophases depending on the number of aromatic rings. Photopolymerization of the discotic complexes was carried out by UV irradiation in the liquid crystalline state. IR and UV-Vis spectroscopy affirmed that diacetylene and acryloyl groups were selectively Polymerized, and that crosslinked polymers containing short conjugated diacetylene oligomers were produced by 1,4-addition. X-ray diffraction experiment showed that the columnar order in the discotic complex containing phenyl-pyridine moiety was maintained after photopolymerization, and that the rectangular columnar order in he discotic Complex with biphenyl units was changed to the lamellar order.

• Polymer(Korea)
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• v.28 no.6
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• pp.468-477
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• 2004

The polymer blends of waste poly(vinyl chloride) (RPVC) and waste polyethylene (RPE) were prepared by melt mixing. Various ethylene-vinyl acetate copolymers (EVA) and ethylene-methacrylic acid Na salt copolymer (ionomer) were used as compatibilizer. Their morphologies and mechanical properties were evaluated as a funtion of mixing sequence and time. EVA with high vinyl acetate contents showed a rapid increment of tensile properties when small amount was added. Tensile properties of the blends were gradually increased with the addition of ionomer. Morphologies of RPVC/RPE blends were analyzed by scanning electron microscopy. FT-IR data showed that EVA was a good compatibilizer in RPVC/RPE blend compared to ionomer. Mechanical properties of the blends were highly enhanced when RPVC and compatibilizer were mixed and first RPE was added later.

• Polymer(Korea)
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• v.39 no.2
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• pp.219-224
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• 2015

In this work, the effect of fiber array direction including $0^{\circ}$, $0^{\circ}/90^{\circ}$, $0^{\circ}/45^{\circ}/-45^{\circ}$ was investigated for mechanical properties of basalt fiber-reinforced composites. Mechanical properties of the composites were studied using interlaminar shear strength (ILSS) and critical stress intensity factor ($K_{IC}$) measurements. The cross-section morphologies of basalt fiber-reinforced epoxy composites were observed by scanning electron microscope (SEM). Also, the surface properties of basalt fibers were determined by Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). From the results, it was observed that acid treated basalt fiber-reinforced composites showed significantly higher mechanical interfacial properties than those of untreated basalt fiber-reinforced composites. These results indicated that the hydroxyl functional groups of basalt fibers lead to the improvement of the mechanical interfacial properties of basalt fibers/epoxy composites in the all array direction.

• The Bulletin of The Korean Astronomical Society
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• v.41 no.1
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• pp.60.1-60.1
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• 2016

태양과 같은 별의 형성기작은 질량이 큰 별의 형성기작에 비해 비교적 잘 연구되어 왔다고는 하지만, 이 또한 온전한 이해와는 거리가 먼 상황이며 여전히 논란의 대상이다. IRAS, Spitzer와 같은 적외선우주망원경으로 얻어진 원시성의 광도함수는 일반적으로 받아들여졌던 별탄생 이론으로 설명되지 못한다는 것이 밝혀졌고, 이에 새로운 별탄생 이론이 필요하게 되었다. 새롭게 받아들여지고 있는 별탄생 모델은 Episodic Accretion 모델로서, 원시행성계원반에서 원시성으로 질량 강착이 간헐적이면서 폭발적으로 일어난다는 것이다. 이러한 모델의 관측적 증거의 하나는 FU Orionis와 같은 천체로서, T-Tauri 단계에 있는 원시성이 본래의 밝기보다 약 100배, 즉 가시광에서 5등급 이상 폭발적으로 밝아진 천체이다. 질량강착의 과정은 행성형성의 초기조건을 결정하는 원시행성계원반의 물리적, 화학적 특성을 결정하므로, 그 이해가 중요하다. 따라서 본 연구팀은 Episodic Accretion이 원시행성계원반과 원시항성풍의 형성과 진화에 어떤 역할을 하는지 연구하기 위하여, 보현산 천문대의 고분산 분광기인 BOES를 이용하여, 최근에 폭발을 일으킨 원시성인 HBC 722와 2MASS J06593158-0405277을 모니터링 관측을 해왔으며, 이전에 알려진 6개의 FU Orionis 형 천체들도 관측하였다. 여기서는 그 결과를 발표하고자 한다.

• Journal of the Korean Chemical Society
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• v.61 no.6
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• pp.339-345
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• 2017

Carbonaceous adsorbent (CA-WTP) was prepared by heat treatment at $400^{\circ}C$ for 2 h in N2 atmosphere using waste tire powder (WTP). WTP and CA-WTP were first characterized by thermo-gravimetric analysis (TGA), energy dispersive X-ray spectrometer (EDS), scanning electron microscopy (SEM), specific surface area analysis (BET) and FT-IR spectroscopy. Then, they were tested as adsorbents for removal of Cd in water. CA-WTP exhibited much higher specific surface area and total pore volume than WTP itself and showed higher adsorption capacity for Cd. Equilibrium data of adsorption were analyzed using Freundlich and Langmuir isotherm models. It was seen that both Freundlich and Langmuir isotherms have correlation coefficient $R^2$ value larger than 0.95. The results of studies indicate that CA-WTP developed from WTP by heat treatment could be used as efficient adsorbent for the removal Cd from water.

• Journal of the Korean Chemical Society
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• v.39 no.11
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• pp.837-841
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• 1995

Thermodynamic parameters for the hydrogen bonding between thiopropionamide(TPA) and proton donors such as triethylphosphine oxide(TEPO), triphenylphosphine oxide(TPPO), trimethylphosphate(TMP), and tributyl phosphate(TBP) in dilute carbon tetrachloride solution have been measured by near-IR spectroscopy. The νa + amide Ⅱ combination band of TPA has been resolved into two Lorentzian-Gaussian product components which have been identified with monomeric TPA and 1 : 1 hydrogen bonded complex. The equilibrium constants and thermodynamic parameters for the formation of 1 : 1 hydrogen bonded complex have been obtained by the analysis of concentration and temperature dependent spectra. The standard enthalpies for the 1 : 1 hydrogen bonded complex formation of TPA with TEPO, TPPO, TMP, and TBP in CCl4 have been found to be - 21.4, - 16.8, - 12.8, and - 12.9 kJ/mol, respectively. The results are explained by the inductive and steric effects of substituents.

• Polymer(Korea)
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• v.36 no.4
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• pp.461-469
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• 2012

The surface modification and characterization of Ar-plasma treated polypropylene (PP) blend are investigated using x-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and contact angle measurement. An increase in Ar-plasma treatment time leads to an increase in wettability, oxygen containing polar functional groups, the amount of talc, and surface roughness on the PP blend surface. A careful observation using SEM indicates that there exists a skin layer consisting of only PP component. The difference in viscosity between PP and rubber particles facilities the formation of skin layer. However, it is found that an increase in Ar-plasma treatment time helps to decrease the thickness of skin layer. Additional methodologies for the elimination of skin layer during injection molding are also discussed. The surface modification and morphological alteration induced by Ar-plasma treatment provides a hydrophilic state, followed by the improvement in wettability, on the PP blend surface.

• Analytical Science and Technology
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• v.16 no.3
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• pp.218-225
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• 2003

Hydrogen Chloride is among the most problematic gases used in semiconductor process. It raises serious environmental and health problems due to its extreme toxicity. This study is to develop a method to effectively remove hydrogen chloride gas during the process by using various types of inorganic gas adsorption agents, which have not been attempted in the conventional methods. The removal efficiency of the gas was both qualitatively and quantitatively measured by a FT-IR spectrophotometer. The whole device for the measurement has been designed and built in our lab. The removal efficiencies of hydrogen chloride gas were compared between those tested resins; zeolite A, modified AgA zeolite, ZnO, and $AgMnO_3$. The experimental result revealed that ZnO showed the best efficiency that had removed 0.067 g of HCl per 1 g of the resin used.

• Journal of the Korean Applied Science and Technology
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• v.31 no.3
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• pp.337-344
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• 2014

In this paper, we have examined the interaction of low bandgap polymer {poly(2-heptadecyl-4-vinylthieno[3,4-d]thiazole)(PHVTT)} with ionic liquids. Further, we have studied the temperature dependent interactions between the ionic liquids [tri-butyl methyl ammonium methyl sulfate ([TBMA][$MeSO_4$]), methyl imidazolium chloride ([MIM]Cl) and butyl methyl imidazolium chloride ([BMIM]Cl)] and polymer using UV-vis spectroscopy, FT-IR spectroscopy, photoluminescence (PL) spectroscopy, as a function of temperature at 21, 28, 32, $37^{\circ}C$. These experimental results suggest that interactions of polymer with ionic liquids ([MIM]Cl, [TBMA][$MeSO_4$]) showed weak interactions by increasing temperature but [BMIM]Cl has no significant effect with increase in temperature.