• 한국응용과학기술학회지
• /
• 제17권1호
• /
• pp.23-28
• /
• 2000

The influence of the polarity of the spreading solvent on the properties of the monolayer of poly(styrene-co-acrylonitrile)'s with various acrylonitrile contents was studied. The surface pressure - area isotherm and the apparent dipole moment - area isotherm were obtained and analyzed when the mixtures of methylene chloride and N-N-dimethylformamide used as spreading solvent. The isotherms were strongly influenced by the polarity of the solvent.

• Bulletin of the Korean Chemical Society
• /
• 제29권1호
• /
• pp.181-186
• /
• 2008

2,5-Di-(2'-hydroxyethoxy)-4'-nitrostilbene (3) was prepared and polycondensed with terephthaloyl chloride, adipoyl chloride, and sebacoyl chloride to yield novel T-type polyesters (4-6) containing the NLO-chromophores dioxynitrostilbenyl groups, which constituted parts of the polymer backbones. Polymers 4-6 are soluble in common organic solvents such as acetone and N,N-dimethylformamide. They showed thermal stability up to 260 oC in thermogravimetric analysis with glass-transition temperatures obtained from differential scanning calorimetry in the range 90-95 oC. The second harmonic generation (SHG) coefficients (d33) of poled polymer films at the 1064 nm fundamental wavelength were around 1.42 ´ 10-9 esu. The dipole alignment exhibited high thermal stability up to 5 oC higher than glass-transition temperature (Tg), and there was no SHG decay below 100 oC due to the partial main-chain character of polymer structure, which is acceptable for NLO device applications.

• The International Journal of Costume Culture
• /
• 제5권2호
• /
• pp.53-65
• /
• 2002

Morphology of polyester fiber was physically modified by solvent treatment. PET fiber was treated with N,N-dimethylformamide (DMF) at 100, 120, $140^{circ}C$ for 10 minutes without tension. The structural changes in the morphology of DMF-induced modified PET fiber were FTIR and SEM analysis. Also dyeing behavior of DMF-treated polyester fibers with various disperse dyes was studied to detect changes of amorphous area in fine structure. DMF treatment resulted in increases in total void content, degree of crystallinity, trans isomer content, chain folding, segmental mobility and molecular packing, but it resulted in decreases in amorphous orientation, intermolecular forces and individual void size through longitudinal shrinkage, lateral welling and removal of oligomers. Void-size distribution could be estimated from the dye uptake with various sizes of disperse dyes. In contrast to the large increases in dye uptake with small dye molecules, there is no and little dye uptake with the bulkiest dye, which means that void size is bigger or smaller than the volume of each dye. Diffusion rates of dye molecules showed increases. This dyeing study revealed that the disperse dyeing is very effective method for characterizing the internal morphology of polyester fiber.

• 한국신재생에너지학회:학술대회논문집
• /
• 한국신재생에너지학회 2009년도 추계학술대회 논문집
• /
• pp.305-305
• /
• 2009

The carbon nano-structured materials could be applied to the fields of advanced fillers, templates, electrode materials, sensor, storage, and absorption materials. The polyacrylonitrile (PAN) based carbon nano-particles provide the remarkable properties of high specific surface area, large pore volume, chemical inertness, and good mechanical stability. In this study, well-defined carbon nano-particles were obtained through pyrolysis of polyacrylonitrile based particles. The precursor nano-particles were prepared by modified aqueous dispersion polymerization using hydrophilic poly(vinyl alcohol) in a water/ N,N-dimethylformamide mixture media. Synthesized precursor nanoparticles have relatively monodisperse particles ranging 80 ~ 250nm. Stable spherical particles are obtained without coagulum or secondary particles in our system. The characteristic of the carbon nanoparticles were investigated in terms of surface area, morphology, and size distribution.

• 한국진공학회:학술대회논문집
• /
• 한국진공학회 2012년도 제42회 동계 정기 학술대회 초록집
• /
• pp.532-532
• /
• 2012

탄소 나노튜브(carbon nanotube, CNT)를 사용하여 AC 구동 방식의 organic light emitting devices (OLED)를 만들었다. 이 소자는 ITO가 코팅된 유리 위에 유전체 층, 유기 발광층 그리고 맨 위의 금속 전극 층으로 총 3개의 층으로 구성되어있다. 유전물질로써는 cyanoethyl pullulan (CRS)를 N,N dimethylformamide (DMF) 용매에 녹여 ITO층 위에 코팅하였고, 유기발광 물질로 poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene] (MEH-PPV)를 chloroform (CF)에 녹여 유전체 층 위에 코팅하였다. CNT를 MEH-PPV와 섞어서 유기발광 혼합물을 만들고 난 후, 유전체층 위에 코팅하였다. 마지막으로 알류미늄 전극을 시료 위에 코팅하였다. 소자에서 사용한 MEH-PPV에 의해 나오는 붉은색 발광을 확인 한 결과, CNT를 사용한 OLED 소자가 CNT를 사용하지 않는 소자보다 brightness가 좋았고, 전류도 더 작게 흘렀다. CNT의 농도에 따라 brightness의 변화는 경향을 나타냈다. CNT에 의한 percolation 효과 때문에 이러한 OLED 시료의 성능 향상이 이루어졌음을 입증하는 실험결과를 발표에서 설명할 예정이다.

• Journal of the Korean Wood Science and Technology
• /
• 제22권4호
• /
• pp.51-60
• /
• 1994

Chlorodeoxycellulose derivatives have recently assumed importance since the halogen atoms can be changed with other functional groups to afford new derivatives of cellulose. Also, chlorinated cellulose has been employed as an intermediate in the preparation of various functional cellulose derivatives. In this study chlorodeoxycellulose was prepared by reaction of methylcellulose with mathanesulfonylchloride in N,N-dimethylformamide. Subsequently, conversion of the above chlorinated cellulose to unsaturated celluloseen was carried out by potassium tertiary butoxide in dimethyl sulfoxide. An anhydrocellulose as an intermediate for the reactive functional derivatives was made by simple alkali treatment. Preparation condition of allylated methylcellulose by using allylchloride and its thermal behavior were also described.

• Fibers and Polymers
• /
• 제1권2호
• /
• pp.71-75
• /
• 2000

Intermolecular cyclization of 2-alkylamino-3-chloro-5,6-dicyanopyrazine 2 in the presence of tributylamine in N,N-dimethylformamide (DMF) gave 5,10-disubstituted-2,3,7,8-tetracyano -5,10-dihydrodipyrazino〔2,3-b:2',3'-e]pyrazines 3, which showed strong mesomorphic property and were anticipated as new chromophoric system for functional dye materials. Absorption spectra, fluorescent properties and other physical properties were correlated with their chemical structures. Vanadyl oligomeric porphyrazine with long alkyl groups synthesized from 3 had satisfactory solubility in tetrahydrofuran (THF), diethyl ether and dimethylsulfoxide (DMSO). The syntheses and characterization of vanadyl polymeric porphyrazines derived from 3 with long alkyl groups are reported.

• Bulletin of the Korean Chemical Society
• /
• 제30권12호
• /
• pp.2921-2926
• /
• 2009

Cu-BTC[$Cu_3(BTC)_2(H_2O)_3$, BTC = 1,3,5-benzenetricarboxylate], one of the most well-known metal-organic framework materials (MOF), has been synthesized under atmospheric pressure and room temperature by using ultrasound. The Cu-BTC can be obtained in 1 min in the presence of DMF (N,N-dimethylformamide), suggesting the possibility of continuous production of Cu-BTC. Moreover, the surface area and pore volume show that the concentration of DMF is important for the synthesis of Cu-BTC having high porosity. The morphology and phase also depend on the concentration of DMF : Cu-BTC cannot be obtained at room temperature in the absence of DMF and aggregated Cu-BTC (with low surface area) is produced in the presence of high concentration of DMF. It seems that the deprotonation of benzenetricarboxylic acid by base (such as DMF) is inevitable for the room temperature syntheses.

• Bulletin of the Korean Chemical Society
• /
• 제16권1호
• /
• pp.17-21
• /
• 1995

A new series of polyarylate copolyesters were prepared by melt polycondensation of 1,4-diacetoxy-2,5-(α-phenylisopropyl)benzene with mixture of terephthalic acid and isophthalic acid in varying ratio. And their general properties such as the glass transition temperature, crystalline melting temperature, crystallinity and solubility were studied. The intrinsic viscosity values of the present polymers measured in a mixed solvent of phenol/p-chlorophenol/1,1,2,2-tetrachloroethane ranged from 0.45 to 0.66 depending on the composition and molecular weight. The copolyesters containing greater than 20 mole % of isophthalic acid were found to be amorphous, whereas the homopolymer derived from terephthalic acid was semicrystalline with a melting point of 414℃. The glass transition temperatures of the polymers ranged from 165 to 180℃ depending on the composition. The copolyesters containing 50 mole % and greater of isophthalic acid moiety were soluble at room temperature in such common solvents as tetrahydrofuran, chloroform and N,N-dimethylformamide.

• Bulletin of the Korean Chemical Society
• /
• 제19권11호
• /
• pp.1165-1168
• /
• 1998

2-Tetrahydropyranyl methacrylate with a self-crosslinkable moiety was copolymerized with methyl methacrylate and 4-[(2-methacryloxyethyl)methylamino]-4'-nitrostilbene or 4-[(2-methacryloxyethyl)ethylamino]-4'nitroazobenzene to provide second-order nonlinear optical property. Glass transition temperatures (Tg of the copolymers are around 140 ℃. The copolymers were soluble in common organic solvents such as tetrahydrofuran (THF), cyclohexanone, and N,N-dimethylformamide (DMF). Poling was carried out at 140 ℃ for 20 min and identified with UV-Vis spectroscopy. Electro-optic coefficient (r33) of copolymer was 62 pm/V for polymer 2 at 633 nm, and relaxation did not remarkably occur due to the formation of a crosslinked network at 200 ℃ for 15 min.