• Bulletin of the Korean Chemical Society
• /
• 제34권6호
• /
• pp.1637-1642
• /
• 2013

We carried out the melt copolymerization reactions of 1,2-bis(diethylamino)tetramethyldisilane with several aryldiols such as, 4,4'-biphenol, 4,4'-isopropylidenediphenol, 9H-fluoren-9,9-dimethanol, and 4,4'-(9-fluorenylidene) bis(2-phenoxyethanol) to afford poly[oxy(arylene)oxy(tetramethyldisilylene)]s containing fluorescent aromatic chromophore groups in the polymer main chain: poly[oxy(4,4'-biphenylene)oxy(tetramethyldisilylene)], poly[oxy{(4,4'-isopropylidene) diphenylene}oxy(tetramethyldisilylene)], poly[oxy(9H-fluorene-9,9-dimethylene) oxy(tetramethyldisilylene)], and poly[oxy{4,4'-(9-fluorenylidene)bis(2-phenoxyethylene)}oxy(tetramethyldisilnylene)]. These prepared materials are soluble in common organic solvents such as $CHCl_3$ and THF. The obtained polymers were characterized by several spectroscopic methods such as $^1H$, $^{13}C$, and $^{29}Si$ NMR. Further, FTIR spectra of all the polymers exhibited characteristic Si-O stretching frequencies at 1014-1087 $cm^{-1}$. These polymeric materials in THF showed strong maximum absorption peaks at 268-281 nm, strong maximum excitation peaks at 263-291 nm, and strong maximum fluorescence emission bands at 314-362 nm due to the presence of tetramethyldisilylene and several arylene chromophores in the polymer main chain. TGA thermograms indicated that most of the polymers were stable up to $200^{\circ}C$ with a weight loss of 3-16% in nitrogen.

• Bulletin of the Korean Chemical Society
• /
• 제33권6호
• /
• pp.2031-2036
• /
• 2012

Melt copolymerization reactions of several bis(diethylamino)silane derivatives, bis(diethylamino)methylphenylsilane, bis(diethylamino)methyloctylsilane, 1,2-bis(diethylamino)tetramethyldisilane, and 1,3-bis(diethylamino) tetramethyldisiloxane, with 2,7-dihydroxyfluoren-9-one were carried out to yield poly[oxy(2,7-fluoren- 9-onenylene)oxy(diorganosilylene)]s bearing the fluoren-9-one fluorescent aromatic group in the polymer main chain: poly[oxy(2,7-fluoren-9-onenylene)oxy(methylphenylsilylene)], poly[oxy(2,7-fluoren-9-onenylene) oxy(methyloctylsilylene)], poly[oxy(2,7-fluoren-9-onenylene)oxy(tetramethyldisilylene)], and poly[oxy- (2,7-fluoren-9-onenylene)oxy(tetramethyldisiloxanylene)]. These polymeric materials are soluble in common organic solvents such as $CHCl_3$ and THF. FTIR spectra of all the materials reveal characteristic Si-O-C stretching frequencies at 1012-1018 $cm^{-1}$. In the THF solution, the prepared materials show strong maximum absorption peaks at 258-270 nm, strong maximum excitation peaks at 260-280 nm, and strong maximum fluorescence emission bands at 310-420 nm. TGA thermograms suggest that most of the polymers are essentially stable to $200^{\circ}C$ without any weight loss and up to $300^{\circ}C$ with only a weight loss of less than 5% in nitrogen.

• 대한기계학회논문집B
• /
• 제32권10호
• /
• pp.729-753
• /
• 2008

Oxy-fuel combustion is a reliable way for the reduction of pollutants, the higher combustion efficiency and the separation of carbon dioxide. The review of recent research trends and the prospects of oxy-fuel combustion were presented. The difference in characteristics among oxy-fuel combustion, conventional air combustion, oxy-fuel combustion with flue gas recirculation (FGR) technique was investigated. Recent experiments of oxy-fuel combustion with/without FGR were surveyed in various ways which are optimized burner design, flame characteristics, the soot emission, the radiation effect, the NOx reduction and the corrosion of combustor. Numerical simulation is more important in oxy-fuel combustion because flame temperature is so high that conventional measurement devices have a restricted application. Equilibrium and non-equilibrium chemical reaction mechanisms for oxy-fuel combustion were investigated. Combustion models suitable for the numerical simulation of non-premixed oxy-fuel flame were surveyed.

• E2M - 전기 전자와 첨단 소재
• /
• 제5권2호
• /
• pp.244-251
• /
• 1992

무독성 혼합안정제 Zn/Ca-stearate의 방사선 안정화 효과를 증진시키기 위해서 oxy-methylene, oxy-ethylene 및 oxy-porpylene 구조의 직쇄형 및 고리형 에테르 화합물을 PVC에 배합하여 방사선조사 하였을 때 PVC의 색차변화를 측정하여 이들 에테르 화합물의 방사선 안정화 효과를 비교 검토하였다. 에테르 화합물에서 oxy-ethylene 구조단위수 4이상인 직쇄형 에테르 또는 고리형 에테르와 oxy-propylene 구조단위수 7인 직쇄형 에테르는 매우 우수한 방사선 안정화 효과를 나타내고 있다. oxy-ethylene 또는 oxy-propylene 구조의 에테르의 방사선 안정화는 Zn/Ca-stearate에서 생성되는 ZnCl$_{2}$와 에테르의 주쇄구조 oxy-ethylene 또는 oxy-propylene의 착체반응에 의한 것으로 추정된다.

• 폴리머
• /
• 제26권4호
• /
• pp.468-476
• /
• 2002

순수한 PAN 섬유의 예비산화와 가수분해의 과정을 통하여 제조된 oxy-PAN은 염기와 산용액에 담그었을 때 신장과 수축 거동을 보임이 알려져 있다. 본 연구에서는, 염기 (NaOH) 용매에서 약 30%의 신장과 산 (HCl) 용매에서 30∼50%의 수축 거동을 관찰하였다. 기계적 특성에 대한 실험에서, oxy-PAN 섬유가 수축되었을 때 향상된 기계적 특성을 나타내었다. 이러한 거동과 기계적 특성은 인체의 근육과 선형 구동체의 그것들과 유사하였다. NaOH와 HCl 용액에서 oxy-PAN 섬유의 길이가 변화하는 중요한 요인으로는 친수화 또는 소수화 구조의 전환에 의한 영향이다. 다른 요인으로는 oxy-PAN 섬유와 용액간의 이온과 물의 교환, 이온의 농도차에 의한 삼투압 등이 영향을 준다. Oxy-PAN 섬유의 신장 및 수축과 기계적 특성에 영향을 미치는 여러 가지 요인들을 규명하기 위한 보다 많은 연구가 필요하지만, 본 연구실에서 제조된 oxy-PAN 섬유가 인공 근육 및 선형 구동체로 적용될 수 있는 충분한 가능성이 있음을 제시한다.

• 한국연소학회지
• /
• 제13권1호
• /
• pp.31-43
• /
• 2008

Oxy-fuel flame has a significantly different structure from that of air-fuel flame because of its high temperature. This study is aimed to find out the difference of the oxy-fuel flame structure in order to understand reaction mechanism closely, which is crucial to design real-scale oxy-fuel combustion system. By examining pictures of counterflow flame and LIF images, we found that oxy-fuel flame had two-zone structure: fuel decomposition region and distributed CO oxidation region. In the oxy-fuel flame, OH radical was distributed intensely through the whole flame due to its higher flame temperature than crossover temperature. For showing those features of the oxy-fuel flame, 1 MW scale IFRF oxy-natural gas burner was simulated by conditional moment closure(CMC) model. Calculation results were compared with experimental data, and showed agreements in trend. In the simulated distributions of fuel decomposition/CO oxidation rates, CO oxidation region was also separated from fuel decomposition zone considerably, which showed the two-zone structure in the oxy-fuel flame.

• BMB Reports
• /
• 제35권4호
• /
• pp.353-357
• /
• 2002

Singlet oxygen ($^1O_2$) is highly reactive form of molecular oxygen that may harm living systems by oxidizing critical cellular macromolecules. The oxyR gene product regulates the expression of the enzymes and proteins that are needed for cellular protection against oxidative stress. In this study, the role of oxyR in cellular defense against a singlet oxygen was investigated using Escherichia coli oxyR mutant strains. Upon exposure to methylene blue and visible light, which generates singlet oxygen, the oxyR overexpression mutant was much more resistant to singlet oxygen-mediated cellular damage when compared to the oxyR deletion mutant in regard to growth kinetics, viability and protein oxidation. Induction and inactivation of major antioxidant enzymes, such as superoxide desmutase and catalase, were observed after their exposure to a singlet oxygen generating system in both oxyR strains. However, the oxyR overexpression mutant maintained significantly higher activities of anticxidant enzymes than did the oxyR deletion mutant. These results suggest that the oxyR regulon plays an important protective role in singlet oxygen-mediated cellular damage, presumably through the protection of antioxidant enzymes.

• 폴리머
• /
• 제26권4호
• /
• pp.492-500
• /
• 2002

일반 PAN 섬유를 $240^{\circ}C$에서 산화시킨 후 1 N NaOH 수용액에서 가수분해시켜 oxidized-PAN 섬유 (oxy-PAN)를 제조하였다. 산과 염기용액에서의 oxy-PAN 섬유의 구조를 $^{13}C-NMR$ 분광분석법을 이용하여 분석하였다. 가수분해에 의하여 -COOH 기를 포함하는 oxy-PAN 섬유는 산과 염기 수용액에서 수축 및 팽창 거동을 하였는데, 염기성 수용액에서는 반대전하로 작용하는 $Na^+$이온이 물 분자와 함께 섬유 내부로 침투하면서 팽창하였으며, 산성 수용액에서는 $Na^+$이온이 물 분자와 함께 섬유 기부로 축출되면서 수축하였다. 친수성의 섬유내부로 산/염기 작용기가 자유롭게 침투하여 oxy-PA기 섬유의 화학적인 구조는 쉽게 변화된다는 것을 확인하였으며, 모폴로지도 pH에 의하여 영향을 받는다는 것을 관찰하였다.

• 한국식품과학회지
• /
• 제44권2호
• /
• pp.251-256
• /
• 2012

상백피 추출물의 연구결과로는 항산화효과, 미백, 주름개선 등의 효과가 있는 것으로 확인되었으나 화장품원료로 사용하기 위한 피부자극, 감작연구는 이루어지지 않은 상태이다. 본 연구에서는 guinea pig를 이용하여 피부 자극시험을 평가한 결과 OXY 및 OXY-3 처리군 모두에서 P.I.I 수치 0.5 이하에 해당하는 비자극성으로 판정되었다. 또한 GPMT법을 이용한 피부감작 시험 평가 결과 OXY 및 OXY-3 처리군 모두에서 발적, 홍반, 부종 등이 전혀 관찰되지 않았고, 반응의 빈도도 0%로 나타나 알러지 유발능이 없는 것으로 판명되었다. 결론적으로, 본 시험조건하에서 guinea pig에 대한 상백피 유래 미백성분들은 1% 이하의 농도에서 사용시 무자극성이며 면역반응에 의한 감작성 부작용을 유발하지 않는 것으로 판단되므로 1% 이하의 시료 물질을 화장품 원료 등에 적용시 약물에 의한 피부 자극성 및 면역반응에 의한 피부 감작성 부작용이 나타날 가능성은 비교적 낮을 것으로 판단된다.

• Bulletin of the Korean Chemical Society
• /
• 제32권4호
• /
• pp.1303-1309
• /
• 2011

Melt copolymerization reactions of bis(diethylamino)tetramethyldisiloxane with several aryldiols were carried out to afford poly(carbotetramethyldisiloxane)s containing fluorescent aromatic chromophore groups in the polymer main chain: poly{oxy(4,4'-biphenylene)oxytetramethyldisiloxane}, poly{oxy(1,4-phenylene)oxytetramethyldisiloxane}, poly[oxy{(4,4'-isopropylidene)diphenylene}oxytetramethyldisiloxane], poly[oxy{(4,4'-hexafluoroisopropylidene)diphenylene}oxytetramethyldisiloxane], poly{oxy(2,6-naphthalene)oxytetramethyldisiloxane}, poly[oxy{4,4'-(9-fluorenylidene)diphenylene}oxytetramethyldisiloxane], poly{oxy(fluorene-9,9-dimethylene)oxytetramethyldisiloxane}, and poly[oxy{4,4'-(9-fluorenylidene)bis(2-phenoxyethylene)}oxytetramethyldisiloxane]. These materials are soluble in common organic solvents such as $CHCl_3$ and THF. The FTIR spectra of all the polymers exhibit the characteristic Si-O-C stretching frequencies at 1021-1082 $cm^{-1}$. In the THF solution, the polymeric materials show strong maximum absorption peaks at 215-311 nm, with strong maximum excitation peaks at 250-310 nm, and strong maximum fluorescence emission bands at 310-360 nm. TGA thermograms indicate that most of the polymers are stable up to $200^{\circ}C$ with a weight loss of less than 10% in nitrogen.