• Proceedings of the Korean Fiber Society Conference
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• 1994.10a
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• pp.141-141
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• 1994

• Proceedings of the Korean Fiber Society Conference
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• 2002.04a
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• pp.255-258
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• 2002

폴리에스테르계 고분자를 용융온도 이상에서 가공하면 두 고분자간의 화학적인 상호교환반응이 일어나고, 이러한 상호에스테르 교환반응은 이들의 공중합체를 생성시켜 블렌드계의 상용성을 증대시킬 수 있으며, 구조와 물리적 성질을 상당한 수준까지 변화시킬 수 있기 때문에 용융가공시 중요한 인자가 되고 있다. 일반적으로 상호에스테르 교환반응에 의해 공중합체가 형성될 때 반응초기에는 블록 공중합체가 형성되며, 반응이 진행될수록 랜덤 공중합체가 형성 [1] 되며, 블렌딩 시간, 온도 그리고 조성비에 따라 상호교환방응 정도가 달라지게 된다[2-3]. (중략)

• Applied Chemistry for Engineering
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• v.7 no.3
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• pp.496-503
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• 1996

Aromatic and aliphatic copolyesters for the dispersing agent were synthesized by two stage reaction, esterification and polycondensation. Copolyesters were blended with PET in the melt state and their thermal and rheological properties were investigated. From GPC analysis Mn's and Mw's of copolyesters were about 30000 and 65000g/mol, respectively. From DSC experiment copolyesters had melting range of $90{\sim}150^{\circ}C$. Copolymer composition was in good agreement with comonomer feed ratio from $^1H$-NMR analysis. Copolyesters and SPA (standard sample) were blended with PET in the melt state. From DSC experiment, copolyesters and SPA were miscible with PET. From the dynamic melt viscosity experiment, melt viscosity of blended sample was increased as the content of aromatic copolyester was increased, while it was decreased as the content of aliphatic and SPA were increased. As for volume resistivity of dry color containing carbon black and copolyesters with dispersing time, aromatic copolyester showed highest value. It was conferred from this result that aromatic copolyester was the best dispersing agent for carbon black in PET resin.

• Proceedings of the Korean Society of Dyers and Finishers Conference
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• 2003.04a
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• pp.47-51
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• 2003

배트염료는 일반적으로 일광, 세탁 등에 견뢰하기 때문에 선명한 색조가 얻어지는 목면용 염료로서 사용되어져 왔지만, 합섬섬유에는 염색되어지지 않는다고 일반적으로 생각되어져 왔다. 따라서 합성섬유가 일상생활의 의류에서 다양하게 사용되어지고 있고, 나일론과 폴리에스테르도 정해진 염료로서 염색되고 있다. 나일론의 경우 산성 혹은 금속착염염료, 반응성염료 및 분산염료가 이용되고 있으나, 폴리에스테르는 거의 대부분이 분산염료로 염색되어진다. (중략)

• The Korean Journal of Rheology
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• v.10 no.3
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• pp.143-151
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• 1998

실리콘 오일에 인산처리 셀룰로오스 분말을 분산시킨 비수계 전기유변성(ER) 유체 의 전기유변 거동을 상온에서 최대 2.5KV/mm의 전기장하에서 실험하였다. 넓은 온도 영역 에서 사용이 가증한 비수계 ER 유체를 개발하기 위해 셀룰로오스의 인산 에스테르 반응이 ER 유체의 전기유변효과에 미치는 영향을 조사하였다. 먼저 여러 가지의 인산처리 농도로 처리된 인산처리 셀룰로오스 미립자를 분산시킨 ER 유체를 제조한 후 ER 유체의 유전상수, 전류밀도 및 전기전도도 등과 같은 전기적 특성을 측정하였으며 ER 유체의 전기유변 특성 또한 측정하였다. 인산처리 셀룰로오스가 분산된 비수계 ER 유체의 전류밀도는 셀룰로오스 의 인산 에스테르 반응에서의 인산처리 농도에 의해 조절할수 있음을 알수있었으며 셀룰로 오스의 인산처리 농도가 2.5 M과 3.0 M 사이일 때 인산처리 셀룰로오스가 첨가된 비수계 ER 유체의 전기유변효과 ($\tau$/$\tau$0)가 가장 높게 측정되었다.

• Journal of the Korean Chemical Society
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• v.25 no.4
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• pp.283-290
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• 1981

The reaction rates for the transesterification reaction were measured on the excess sucrose with the five fatty acid methyl ester systems such as methyl laurate, methyl myristate, methyl palmitate, methyl stearate and methyl oleate at temperature range of $50^{\circ}C$ to $90^{\circ}C$ in N,N-dimethylformamide solvent and potassium carbonate as a catalyst. Their activation parameters as well as rate constants were calculated from these measurements. And these reactions were found to be pseudo-first order and depended mainly on the structural changes in fatty acid residue of methyl esters. Also their reactions were found to be of enthalpy-controlled, which were disfavored in the order of methyl laurate, methyl myristate, methyl palmitate, methyl oleate and methyl stearate. Correspondingly their activation energies were 9.3, 9.9, 10.3, 10.9 and 11.1 kcal/mole, respectively.

• Polymer(Korea)
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• v.35 no.2
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• pp.176-182
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• 2011

Liquid crystalline aromatic polyesters (LCPs) are representative examples of thermotropic liquid crystalline polymers, whose structure-property relationships have been the subject of many researches. In this study, we synthesized organo-soluble liquid crystalline aromatic polyesters, and their composites with acetylene-terminated thermoset resins were prepared and characterized. Soluble LCPs were synthesized by employing 6-hydroxy-2-naphthoic acid, terephthalic acid, isophthalic acid, and 4-aminophenol as monomers via condensation polymerization based on transesterfication and transamidation. Acetylene-terminated thermoset resins were synthesized by the reaction of 4-ethynylaniline with terephthaloyl dichloride, isophthaloyl dichloride or 4,4'-biphenyldicarbonyl dichloride. We prepared the soluble LCP/thermoset composites by solution blending followed by thermal treatment. The thermal stability, thermal expansion coefficient, and dielectric properties of the composite were studied.

• Korean Chemical Engineering Research
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• v.51 no.1
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• pp.144-150
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• 2013

The kinetics of the transesterification of dimethyl terephthalate (DMT) with ethylene glycol (EG) was studied in a batch reactor. Bishydroxyethyl terephthalate (BHET), which is poly(ethylene terephthalate) (PET) monomer, can be produced by the transesterification reaction. Zinc acetate was used as a catalyst. Previous kinetic studies was carried out in a semi-batch reactor where generated methanol was removed so that reverse reactions were not considered in the kinetic expressions, resulting in inaccuracy of the kinetic model. Mathematical models of a batch reactor for the tranesterification reaction were developed and used to characterize the reaction kinetics and the composition distribution of the reaction products. More accurate models than previous ones were obtained and found to have a good agreement between model predictions and experimental data. Effect of process variables on the esterification reaction was investigated based on the experimental and simulation results.

• Journal of the Korean Chemical Society
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• v.25 no.6
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• pp.361-366
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• 1981

For the urethane formation reaction of isocyanate with alcohol, orientation of approach of alcohol toward isocyanate was investigated theoretically by means of MO method. As a result of EHT and CNDO/2 calculations, it was found that the reaction proceeding via 4-centered mechanism, in which ROH is coplanar with isocyanate plane was energetically favored. It was also shown that the oxygen of ROH attacks the isocyanate carbon prior to the formation of 4-center complex. The reaction was found to be a charge controlled one.

• Polymer(Korea)
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• v.29 no.3
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• pp.314-319
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• 2005

Four kinds of new aliphatic diols were synthesized by the ring opening reaction of glycolide with 1,4-butanediol, 1,6-hexanediol, 1,4-cyclohexanediol, or 1,4-cyclohexanedimethanol, a difunctional initiator, in the presence of stannous octoate catalyst. The resulting diols were melt-polymerized with succinic acid, adipic acid, or suberic acid at 170, 190, or $220^{circ}C$ to produce new sequentially ordered aliphatic polyesters and their corresponding polyesters with random structure. Their glass transition temperatures ($T_g$) ranged from -40 to $30^{circ}C$, The sequentially ordered polyesters prepared at $170^{cir}C$ had higher $T_g$ of 5 to $10^{circ}$ than the polyesters with rand()m structure produced at higher temperature. From in-vitro degradation test the sequentially ordered polyesters was shower in the rate of hydrolysis in a buffer solution than the polymers with random molecular structure.