• Korean Chemical Engineering Research
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• 제51권3호
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• pp.342-346
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• 2013

온실가스인 $CO_2$를 저감하기 위한 기술로 본 연구에서는 이온성 액체를 이용하여 epoxide계 화합물인 glycidyl methacrylate (GMA)와 $CO_2$의 고리화 첨가 반응(cycloaddition)을 통해 cyclic carbonate를 합성하였다. 합성된 cyclic carbonate인 [2-oxo-1,3-dioxolan-4-yl]methacrylate (DOMA)는 FT-IR과 $^1H$ NMR을 이용하여 그 구조를 확인하였다. 또한 $^1H$ NMR을 통하여 계산된 조성비를 이용하여 전환율과 시간의 관계를 관찰하였다. DOMA로 전환이 모두 이루어진 이후에는 DOMA의 이중결합이 잔존하는 이온성 액체로 음이온 중합, cyclic carbonate ring의 가교반응에 의한 고분자가 형성되었다.

• 한국재료학회지
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• 제34권3호
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• pp.175-183
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• 2024

Geopolymer, also known as alkali aluminum silicate, is used as a substitute for Portland cement, and it is also used as a binder because of its good adhesive properties and heat resistance. Since Davidovits developed Geopolymer matrix composites (GMCs) based on the binder properties of geopolymer, they have been utilized as flame exhaust ducts and aircraft fire protection materials. Geopolymer structures are formed through hydrolysis and dehydration reactions, and their physical properties can be influenced by reaction conditions such as concentration, reaction time, and temperature. The aim of this study is to examine the effects of silica size and aging time on the mechanical properties of composites. Commercial water glass and kaolin were used to synthesize geopolymers, and two types of silica powder were added to increase the silicon content. Using carbon fiber mats, a fiber-reinforced composite material was fabricated using the hand lay-up method. Spectroscopy was used to confirm polymerization, aging effects, and heat treatment, and composite materials were used to measure flexural strength. As a result, it was confirmed that the longer time aging and use of nano-sized silica particles were helpful in improving the mechanical properties of the geopolymer matrix composite.

• Macromolecular Research
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• 제17권10호
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• pp.770-775
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• 2009

$\omega$-Anhydride-functionalized poly(ethylene oxide) (PEO) obtained from chain-end functionalization and anionic ring-opening polymerization of ethylene oxide using n-butyllithium with potassium t-butoxide in the presence of dimethylsulfoxide (DMSO) was found to be an efficient material for the preparation of water-soluble, polymeric pro-drugs. The reaction of $\omega$-anhydride-functionalized PEO with sulfonamide or with vancomycin provided an efficient method to produce corresponding, water-soluble, PEO-conjugated sulfonamide or PEO-conjugated, vancomycin pro-drugs. These were used successfully to prepare water-dispersible, silver nanoparticles. In this study, the particle sizes were in the range of $5{\sim}40$ nm. The resulting products were characterized by $^1H$ NMR spectroscopy, transmission electron microscopy, electron and X-ray diffraction, size exclusion chromatography, and UV/Visible spectroscopy.

• Korean Chemical Engineering Research
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• 제54권1호
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• pp.36-43
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• 2016

Hydrosilylation reactions of 2.4.6.8-tetrahydro-2.4.6.8-tetramethylcyclotetrasiloxane with allyl butyrate catalyzed by Karstedt's, $H_2PtCl_6$ and Pt/C catalyst were studied and 2.4.6.8-tetra (propyl butyrate)-2.4.6.8-tetramethylcyclotetrasiloxane was obtained. The reaction order, activation energies and rate constants were determined. Ringopening polymerization of 2.4.6.8-tetra (propyl butyrate)-2.4.6.8-tetramethylcyclotetrasiloxane in the presence of $CaF_2$, LiF, KF and anhydrous potassium hydroxide in $60-70^{\circ}C$ temperature range was carried out and methylsiloxane oligomers with regular arrangement of propyl butyrate pendant groups were obtained. The synthesized products were studied by FTIR and NMR spectroscopy. The polysiloxanes were characterized by wide-angle X-ray, gel-permeation chromatography and DSC analyses. Via sol-gel processes of oligomers doped with lithium trifluoromethylsulfonate or lithium bis (trifluoromethylsulfonyl)imide, solid polymer electrolyte membranes were obtained. The dependences of ionic conductivity of obtained polyelectrolytes on temperature and salt concentration were investigated, and it was shown that electric conductivity of the polymer electrolyte membranes at room temperature changed in the range $3.5{\times}10^{-4}{\sim}6.4{\times}10^{-7}S/cm$.

• 공업화학
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• 제31권1호
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• pp.30-35
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• 2020

본 연구에서는 폴리우레탄-실리카 복합 발포체를 합성하여 복합 발포체의 단열 특성 및 기계적 물성을 분석하였다. 폴리우레탄-실리카 복합 발포체를 합성하기 위해 폴리에스테르-실리카 복합 폴리올을 합성하였다. 폴리에스테르-실리카 복합 폴리올은 실리카 졸과 모노머 상태의 다이카복실산(dicarboxylic acid), 글리콜(glycol)과의 중합 반응을 통해 합성하였다. 합성된 복합 폴리올을 이용하여 폴리우레탄-실리카 복합 발포체를 합성하여 물성을 분석하였다. 폴리우레탄-실리카 복합 발포체의 열전도도는 HPUF0, HPUF1, HPUF3, HPUF5 모두 큰 차이가 없는 것을 확인하였다. 압축강도는 실리카 함량이 증가함에 따라 HPUF0보다 증가하였으며 HPUF0보다 HPUF5가 약 25% 정도 기계적 물성이 향상되는 것을 확인하였다.

• Journal of Korean Dental Science
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• 제6권2호
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• pp.41-49
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• 2013

Purpose: This study sought to compare the elemental constitution, morphological characteristics, particle size distribution, biocompatibility, and mineralization potential of Ortho MTA (OMTA) and ProRoot MTA (PMTA). Materials and Methods: OMTA and PMTA were compared using energy-dispersive spectrometry, particle size analysis, and scanning electron microscopy. The biocompatibility and mineralization-related gene expression (osteonectin and osteopontin) of both MTAs were also compared using methylthiazol tetrazolium assay and reverse transcription-polymerization chain reaction analysis, respectively. The results were analyzed by Kruskal-Wallis test with Bonferroni correction. P-value of <0.05 was considered significant. Result: The morphology of OMTA powders was similar to that of PMTA. The constituent elements of both MTAs were calcium, silicon, and aluminum. The mean particle sizes of OMTA and PMTA were 4.60 and 3.34 mm, respectively. Both MTAs had equally favorable in vitro biocompatibility and affected the messenger RNA expression of osteonectin and osteopontin. Conclusion: Within the limitations of this study, OMTA could be a promising biomaterial in clinical endodontics.

• Bulletin of the Korean Chemical Society
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• 제32권5호
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• pp.1613-1619
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• 2011

A hybrid thermosetting maleimido epoxy compound 4-(N-maleimidophenyl) glycidylether (N-MPGE) containing Co(II), Ni(II) and Cu(II) ions was prepared by curing N-MPGE and tetradentate Schiff base Co(II), Ni(II) and Cu(II) complexes. The curing polymerization reaction of N-MPGE with metal complexes as curing agents was studied. The cured samples were studied for thermal stability, chemical (acid/alkali/solvent) and water absorption resistance and homogeneity of the cured systems. The tetradentate Schiff base, 3-[(Z)-2-piperazin-1-yl-ethylimino]-1,3-dihydro indol-2-one was synthesized by the condensation of Isatin (Indole-2, 3-dione) with 1-(2-aminoethyl)piperazine (AEP). Its complexes with Co(II), Ni(II) and Cu(II) have been synthesized and characterized by microanalysis, conductivity, Uv-Visible, FT-IR, TGA and magnetic susceptibility measurements. The spectral data revealed that the ligand acts as a neutral tetradentate Schiff base and coordinating through the azomethine nitrogen, two piperazine nitrogen atoms and carbonyl oxygen.

• Bulletin of the Korean Chemical Society
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• 제25권7호
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• pp.983-985
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• 2004

PMMA-coated CdS nanorod was prepared by encapsulation of CdS nanorod through the polymerization process of PMMA on the surface of CdS nanorod. PMMA organic nanotube was then obtained from the elimination of the CdS nanorod by the photocorrosion. For the photocorrosion reaction of the CdS nanorod, monochromatic light was irradiated to the oxygen-saturated aqueous methyl viologen solution with PMMAcoated CdS nanorod. Photocorrosion reactions of PMMA-coated CdS nanorod were investigated and characterized by utilizing UV-Vis absorption, X-ray diffraction (XRD) and scanning electron microscopic (SEM) and transmission electron microscopic (TEM) images.

• 한국세라믹학회지
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• 제40권4호
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• pp.385-392
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• 2003

Sol-gel preparation technique using a chemical reaction of metal alkoxides has been widely used for the fabrication of various materials including ceramics. However, its mechanism has been studied till now because a number of chemical ways are possible from various alkoxides and additives. In this study, the mechanism of hydrolysis, condensation, and polymerization of alkoxides were investigated from the fabrication of lead-zirconate-titanate (PbZr$\_$x/Ti$\_$l-x/O$_3$; PZT) thin film that is used as various micro-actuator, transducer, and sensor because of its high electro-mechanical coupling factors and thermal stability. Furthermore, the fabrication process and characteristics of self-patternable PZT film using photosensitive stabilizer were studied in order to resolve the problem of physical damage and properties degradation during dry etching for device fabrication. Using an optimum condition to prepare the self-patternable PZT film, more than 5000 ${\AA}$ thick self-patternable PZT film could be fabricated by three times coating. The PZT film showed 28.4 ${\mu}$c/cm$^2$ of remnant polarization (Pr) and 37.0 kV/cm of coercive field (E$\_$c/).

• 공업화학
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• 제17권4호
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• pp.426-431
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• 2006

Poly(methyl methacrylate) (PMMA)의 착색을 위하여 아크릴 그리고 비닐설폰기를 가지는 청색 및 오렌지 아조 염료들을 6-bromo-2-cyano-4-nitroaniline과 2,5-dimethoxy-4-(vinylsulfonyl)benzenamine을 3-acrylamido-(N,N-diethylamino) benzene과 3-methyl-(N,N-diethylamino)benzene의 아조 짝지음 반응을 이용하여 각각 합성하였다. 또한 알릴기를 가지는 염료는 비닐설폰과 allylamine과의 반응에 의하여 제조하였다. PMMA의 착색은 아크릴, 비닐설폰 그리고 알릴 작용기를 가지는 염료를 직접 methyl methacrylate (MMA)와 공중합하거나, MMA와 공중합한 고분자염료 및 반응성기가 없는 염료 2를 직접 MMA에 용해하여 중합과 동시에 착색하였다. 3가지로 착색한 PMMA의 염색 견뢰도를 여러 환경 조건에서 염료의 용해도를 비교하여 평가하였다.