• 폴리머
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• 제29권6호
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• pp.523-535
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• 2005

선형 방향족 폴리에스테르는 열방성 액정중합체의 대표적 예로 지금까지 그 구조-액정성 관계가 많이 연구되었다. 본 논문에서는 지난 4반세기 동안 본 연구진이 행한 연구결과를 중심으로 액정성 전방향족 폴리에스테르의 열적특성 및 액정성을 그 화학구조와 관련지어 논의한다. 특히 미세화학구조의 변경이 어떻게 액정성에 영향을 주는가에 논의의 초점을 두었다. 특히 선형구조에서 크게 벗어나는 복합형 액정성 폴리에스테르 및 액정성 고차가지구조 폴리에스테르도 조감하였다. 고차가지구조 고분자는 덴드리머와 관련하여 많은 관심을 끌고 있다. 이 고분자들의 합성법도 말미에 소개하고 있다.

• 한국염색가공학회지
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• 제16권1호
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• pp.18-25
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• 2004

In this study, the effect of microwave which can increase temperature rapidly on polyester alkaline dyeing was investigated. The final K/S values of polyester fabrics dyed by microwave lower than those of atmospheric dyeing because of the evaporation loss of dyeing solution. If the dyeing time makes longer as much as that in atmospheric dyeing, the K/S values of polyester fabrics dyed under microwave were similar to those of atmospheric dyeing. The K/S values of polyester fabrics dyed in pH 9.5 were higher than those in pH 5.5 in case of aliphatic carriers. The K/S values of organic reagent pretreated polyester fabrics dyed by use of aromatic carriers were not higher than those of non-treated polyester fabrics. But the K/S values of polyester fabrics dyed by use of aliphatic carriers were higher than those of non-treated polyester fabrics. The tensile strength were decreased with increasing of dyebath pH because the polyester fabrics were easily decomposed by high alkali.

• 공업화학
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• 제3권4호
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• pp.694-700
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• 1992

Palladium 촉매에 의한 CO Insertion Heck reaction을 고분자 중합에 응용하여 가공성이 좋은 고강도 엔지니어링 플라스틱으로 응용 가능한 flexible spacer를 가진 aromatic polyamide와 Polyester를 합성할 수 있었다. 촉매로서 dichlorobis(triphenyl phosphine) palladium(II) $(PdCl_2(PPh_3)_2)$와 Palladium chloride($PdCl_2$)를 사용하였고, 이 중합 시스템은 똑같은 조건에서 polyamide와 polyester를 합성 할 수 있는 장점이 있으므로 그 중합체의 열적성질을 DSC, TGA 등으로 조사하였는데 곁사슬이 있지 않은 aromatic polyamide와 Polyester는 amide와 ester 결합의 차이에도 불구하고 전이온도등이 거의 같았다. Hexyl부터 hexadecyl까지 alkyl 곁사슬을 2,5 위치에 이중으로 가진 phenylene dibromide와 Phenylene diamine으로부터 중합체를 합성하였는데 치환기가 없는 경우에 비하여 전이온도가 감소하였고, alkyl side chain이 hexadecyl인 경우는 뚜렷한 융점을 확인할 수 있었다.

• Elastomers and Composites
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• 제46권2호
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• pp.158-163
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• 2011

해수 하에서 경시 변화에 따른 경질 폴리우레탄 폼(PUF)의 물성 변화를 알아보기 위해 방향족 폴리에스테르 폴리올, 지방족 폴리에스테르 폴리올과 지방족 폴리에테르 폴리올 함량에 따라 경질 폴리우레탄 폼을 합성하였다. 해수 하에서 PUF의 물성변화를 고찰하기 위해 만능시험기, 시차 주사 열량계, 경도 측정기, 적외선 분광계를 이용하였다. 방향족 폴리에스테르 폴리올의 함량이 증가함에 따라 해수 하에서 경시 변화에 따라 PUF의 압축강도와 경도의 감소폭은 증가하였다. 해수 하에서 PUF의 유리전이온도는 증가하였는데 적외선 스펙트럼 분석 결과 우레탄과 우레아의 피크는 감소하고, 알로파네이트와 바이우렛의 피크는 증가한 것을 알 수 있었다. 해수 하에서 PUF는 가교도가 증가하여 폼이 brittle하게 형성됨에 따라 유리전이온도가 증가하였지만 가수 분해로 인하여 기계적 물성이 저하된 것으로 사료 된다.

• Macromolecular Research
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• 제8권1호
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• pp.12-18
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• 2000

Six aromatic polyesters with ether-linkages were prepared from 4,4'-oxybis(benzoic acid) and naphthalenediol (ND) isomers which were 1,4-, 1,5-, 1,6-, 2,3-, 2,6- and 2,7-derivatives. The solution viscosity numbers ranged from 0.23 to 0.65 dL/g. The glass transition temperatures ranged from 142 to 179$\^{C}$. The initial decomposition temperatures were all above 400$\^{C}$, and the residue weights at 600$\^{C}$ were in the range of 50-64%. Only the polyesters derived from 1,5- and 2,6-NDs, which have a linear linking mode, were found to be semicrystalline and could form thermotropically nematic phase. Multiple melting phenomena and annealing of the polyester derived from 1,5-ND and related polymers are described. The experimental results show that the polyester derived from 1,4-ND of linear shape was amorphous and non-liquid crystalline. Particularly, the polyester derived from 2,3-ND could form a smectic mesophase as banana-shaped molecules, and this is ascribed to the C/sub_2v/ symmetry where highly kinked molecules are packed in the same direction.

• Macromolecular Research
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• 제17권5호
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• pp.289-295
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• 2009

Low viscosity aromatic hyperbranched polyester epoxy resin (HTBE) was synthesized by the reaction between epichlorohydrin (ECH) and carboxyl-end hyperbranched polyester (HTB) which was prepared from inexpensive materials $A_2$ (1,4-butanediol glycol, BEG) and $B_3$ (trimellitic anhydride, TMA) by pseudo one-step method. The molar mass of the HTB was calculated from its acid value by "Recursive Probability Approach". The degree of branching (DB) of the HTB was characterized by model compounds and $^1H$ NMR-minus spectrum technology, and the DB of the HTB was about $0.47{\sim}0.63$. The viscosity and epoxy equivalent weight of the HTBE were $3,600{\sim}5,000\;cp$ and lower than 540 g/mol respectively. The reaction mechanism and structure of the $AB_2$ monomer, HTB and HTBE were investigated by MS, $^1H$ NMR and FTIR spectra technology. The molecular size of HTBE is under 8.65 nm and its shape is ellipsoid-like as determined by molecular simulation.

• 한국섬유공학회:학술대회논문집
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• 한국섬유공학회 1997년도 춘계학술발표회 논문집
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• pp.328-332
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• 1997

Hot stretching focused on the improvement of properties of poly(L-lactic acid) fiber. Some aliphatic polyesters are biodegradable under microbial attack and the new unique applications are expected. Generally, these materials have a somewhat low melting temperature and low mechanical properties compared with the aromatic polyesters. In this study, melt-spinning of poly(L-lactic acid) was conducted. We investigated effects of the stretching and the molecular orientation of aliphatic polyester fibers on the change of fine-structure. Glass transition temperature, molecular orientation and crystallinity increased according to the increase of stretching ratio.

• 폴리머
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• 제31권5호
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• pp.442-446
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• 2007

알칼리 가용성, 광경화형 폴리에스터를 합성하기 위해 플루오렌형 에폭시 아크릴레이트에 다양한 산 2 무 수물을 반응시켰다. LCD (liquid crystal display) 컬러 필터용 블랙매트릭스를 제조하기 위해서 합성된 폴리에스터와 카본블랙 등을 혼합하여 포토레지스트 용액을 조제한 후 리소그래피 공정을 통해 유리 기판 위에 블랙매트릭스패턴을 형성하였다. 합성된 다양한 폴리에스터의 특성과 리소그래피 패턴을 비교 조사하였다.

• 한국응용과학기술학회지
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• 제19권1호
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• pp.25-32
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• 2002

Two PU flame-retardant coatings, 2,3-DBPO/N-l00 (DBPON) and 2,3-DBPO/IL (DBPOI), were prepared by curing 2,3-dibromo modified polyester (2,3-DBPO) with isocyanate curing agent Desmodur N-l00 (or Desmodur IL) at room temperature. The physical properties and flame-retardancy of the two coatings were tested and compared. As a result, the pot-life, yellowness index, lightness index difference, $60^{\circ}$ specular gloss, cross-hatch adhesion, viscosity, and accelerated weathering resistance of DBPON were better than those of DBPOI; the fineness of grind of the two coatings were the same; and the drying time, hardness, and abrasion resistance of DBPOI were better than those of DBPON. The flame retardancy of the flame-retardant coatings increased with the content of the flame retarding component, 2,3-dibromopropanoic acid (2,3-DBP); and the LOI values of the two coatings were in a range of $27{\sim}29%$ when the content of 2,3-DBP was 30wt%.

• Macromolecular Research
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• 제12권2호
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• pp.195-205
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• 2004

We have synthesized new aromatic polyesters (DiPEG-HQ and DiPEG-BP) by condensation polymerization of a terephthalic acid derivative bearing a pendant oligo(oxyethylene) (DP = 7, MW = 350), which has a methoxy terminal group, and two different aromatic diols, hydroquinone and 4,4'-biphenoI. The synthesized polymers were characterized by differential scanning calorimetry (DSC), polarizing microscopy, and X-ray diffractometry for their liquid crystallinity (LC), thermal transitions, and structural morphologies in mesophases. The morphology of the LC phases depends strongly on the length of the rigid backbone repeating unit. The DiPEG-BP polymer having a longer repeating unit exhibits both layered and nematic structures before isotropization, whereas the DiPEG-HQ polymer having a shorter repeating unit shows only the layered structure in the mesophase. We found that the layer spacing for DiPEG-HQ is larger than that for DiPEG-BP. Both polymers easily form complexes with LiCF$_3$SO$_3$; we studied this complex formation by FT-IR spectroscopy. The layer spacing of the polymer-electrolyte composites increases upon increasing the amount of the lithium salt. The polymer/salt electrolyte mixtures we investigated at molar ratios of EO:salt in the range of 5-20 exhibit electrical conductivity values at 40$^{\circ}C$ of 2.4${\times}$10$\^$5/ and 1.1${\times}$10$\^$－5/ S/cm for DiPEG-HQ/LiCF$_3$SO$_3$ and DiPEG-BP/LiCF$_3$SO$_3$, respectively. At 80 $^{\circ}C$, these values are higher: 4.6${\times}$10$\^$－3/ and 1.1${\times}$10$\^$－4/ S/cm, respectively. The activation energy of conductivity depends strongly on the salt concentration.