• 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.

• 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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• 제24권3호
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• pp.358-365
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• 2000

Miscibility itnd thermal behavior of blends of synthetic biodegradable aliphatic polyester (Bionolle) with poly(epichlorohydrin) (PECH) were investigated by a differential scanning calorimetry (DSC), a dynamic mechanical thermal analyzer (DMTA) and a rotational rheometer. Observed both single glass transition temperatures from the DSC in agreement with the Fox equation and single T$_{g}$ changes as a function of composition from the DMTA indicate that these blend mixtures are miscible. In addition, the miscibility of this blend system was also observed from the single curve of the Cole-Cole Plot of log G′($\omega$) vs. log C"($\omega$) from the dynamic test using a rotational rheometer. This was further verified from the cryogenically fractured surface of BDP/PECH blends by scanning electron microscopy.

• 폴리머
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• 제34권5호
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• pp.424-429
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• 2010

졸-젤법을 이용한 실리카를 지방족 폴리에스테르 주사슬에 가교구조로 도입한 하이브리드 복합재료를 합성하여 열전소자의 버퍼코트층으로의 적용가능성을 검토하였다. 고분자 기지로 사용된 폴리에스테르는 $240^{\circ}C$의 고온에서 열처리 시간에 따라 $30{\sim}90^{\circ}C$ 정도 열분해개시 온도가 증가하였고, 폴리에스테르-실리카 복합재료는 실리카의 첨가 비율에 따라 $30{\sim}50^{\circ}C$ 정도 열분해 개시온도가 증가하였다. 폴리에스테르-실리카 복합재료는 실리카가 Knoevenagel 축합반응을 방해하는 요소로 작용하여 폴리에스테르에 비해 열처리후에도 변색이 일어나지 않았고, 광학특성 변화가 작았다. 이들 복합재료의 열전도도는 실리카의 첨가량에 따라 선형적으로 증대되었다.

• 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.

• 한국섬유공학회:학술대회논문집
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• 한국섬유공학회 1992년도 제1차 학술발표초록집
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• pp.47-47
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• 1992

• 한국고분자학회지:고분자과학과기술
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• 제5권1호
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• pp.13-18
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• 1994

• Macromolecular Research
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• 제14권2호
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• pp.179-186
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• 2006

In the present work, low density polyethylene (LDPE)/aliphatic polyester (APES)/organoclay ternary nanocomposites were prepared. In particular, the effect of a compatibilizer, polyethylene-graft-maleic anhydride (PE-g-MAH), on the morphology and properties of the ternary nanocomposites was investigated. LDPE/APES/organoclay nanocomposites were prepared through melt intercalation method using two different kinds of organoclay. The dispersibility of silicate clays in the nanocomposites was investigated by X-ray diffraction and atomic force microscopy. The ternary nanocomposites showed higher tensile properties than the LDPE/APES blend did. The dispersibility and properties of nanocomposites containing Cloisite 30B were better than those of the nanocomposites containing Cloisite 20A. Unlike Cloisite 20A, hydroxyl groups in the intercalants in Cloisite 30B interlayer underwent a certain polar interaction with the carboxyl group of APES, favoring the intercalation of APES chains and the formation of LDPE/APES/Closite 30B nanocomposites. However, the introduction of the polar hydroxyl groups also enhanced the interaction with the silicate surface at the same time, thereby rendering somewhat difficult the replacement of the surface contacts by LDPE chains, and impeding the extensive intercalation and further exfoliation of Cloisite 30B in the LDPE/APES matrix. The compatibilizer enhanced the intercalation of the polymer chain inside the clay gallery and thus improved the mechanical properties of the ternary nanocomposites. Rheological measurements of the nanocomposites via frequency sweep experiment indicated a certain interaction between the clay platelet and the polymer molecules in the melted state.

• 폴리머
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• 제24권2호
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• pp.281-286
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• 2000

분자량이 각각 500, 1000, 2500인 비정형 polyether와 sebacoyl chloride로부터 분자량이 약 8000~15000정도인 지방족 폴리에스테르 공중합체를 합성하였으며, $^1$H-NMR과 FT-IR을 이용하여 구조와 조성을 분석, 확인하였다. 합성된 폴리에스테르의 경우, 3가지 시료 모두 결정은 관찰되지 않았으며 사용된 polyether의 분자량에 관계없이 유리전이온도가 약 -77$^{\circ}C$인 완전한 비정형 물질을 얻을 수 있었다. 반면에 poly(ethylene glyool) (PEG)을 이용한 경우는 사용한 PEG의 분자량이 증가함에 따라 공중합체의 융점과 결정화도가 증가함을 알 수 있었다. 분자량이 200과 400인 PEG를 이용한 경우에는 약 -71$^{\circ}C$ 정도의 유리전이온도를 보였으며, 융점은 -42.4$^{\circ}C$와 -22.4$^{\circ}C$에서 관찰되었다. 그러나 분자량이 1000인 PEG를 이용한 경우에는 융점이 23.$0^{\circ}C$로 나타났다. 또한 사용된 PEG의 분자량이 증가할수록 공중합체의 결정화도는 8.8%, 16.2%와 46.7%로 증가하였다.

• Bulletin of the Korean Chemical Society
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• 제33권8호
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• pp.2560-2566
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• 2012

The present study investigates how the thermal stability of retinol (vitamin A) encapsulated in polyester nanoparticles is influenced by the types of polyester used for the nanoparticles. A variety of polyester-retinol nanoparticles were prepared with various polyesters like: poly(ethylene adipate), PEA; poly(butylene adipate), PBA; poly(hexamethylene adipate), PHMA; and three polycaprolactones, PCL, of different molecular weights ($M_n$ ~10, 40, and 80K). The chemical stability of retinol in these nanoparticles, monitored in an aqueous solution at $25^{\circ}C$ and $40^{\circ}C$ for 4 weeks, was high in the following order of the nanoparticles prepared with PHMA > PCL 40K > PCL 10K > PCL 80K > PBA~PEA at $25^{\circ}C$ and PCL 10K > PCL 40K > PHMA > PCL 80K > PEA > PBA at $40^{\circ}C$. More importantly, this study has also found that the thermal stability of the retinol in the nanoparticles was closely connected with the melting temperatures of polyesters and polyester nanoparticles. The results were further discussed with possible factors - such as sample preparation condition (or history) and miscibility between the polyesters and retinol - affecting $T_m$ of the polyesters and the nanoparticles.