• Elastomers and Composites
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• 제40권1호
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• pp.37-44
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• 2005

새로운 형태의 액정성 폴리우레탄을 2,6-bis(${\omega}$-hydroxyalkoxy)naphthalene (BHNm; m= 5, 6, 8, 11)과 2,5-tolylene diisocyanate 또는 1,4-phenylene diisocyanate의 중부가 반응에 의해 합성하였다. 폴리우레탄의 고유 점성도는 0.28-0.43 dL/g 였다. 열적 성질은 DSC 및 편광현미경에 의해 측정되었다. 단량체 BHNm과 메틸치환기를 가진 2,5-tolylene diisocyanate에 의해 합성된 폴리우레탄은 모두 단방성 액정성을 나타내었다. 그러나 BHNm와 1,4-phenylene diisocyanate를 합성한 폴리우레탄에서는 DSC와 편광현미경으로 조사 결과 전혀 액정성을 나타내지 않았다.

• 한국염색가공학회지
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• 제8권2호
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• pp.1-7
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• 1996

Thermotropic liquid-crystalline polyurethanes were synthesized by the polyaddition reaction of such para-substiuted diisocyanate monomer as 1,4-phenylene diisocyanate(1,4-PDI) and 2,5-tolylene diisocyanate(2,5-TDI), with 4,4'-bis($\omega$-hydroxyalkoxy)biphenyls(BPm: $HOC_{m}OC_{6}H_{4}C_{6}H_{4}OC_{m}H_{2m}OH$; m is the carbon number of the hydroxyalkoxy group). These polyurethanes have mesogenic biphenyl units in the main chain. Properties of polymers were studied by differential scanning calorimetry, wide-angle X-ray scattering, thermogravimetic analysis, polarizing microscopy, and infraed spectroscopy. DSC thermograms for these polymers exhibited two endothermic peaks corresponding to phase transitions of melting and isotropization. Mesomorphic behavior of the polyurethanes were also observed under the polarizing microscope. For example, polyurethane 2,5-YDI/BP5 with [$\theta$]=0.44 prepared from 2,5-TDI and BP5 exhibited a liquid crystalline phase from 194 to 205$^{\circ}C$. Infrared spectrum study indicated that the hydrogen bonding between urethane linkages affected the mesomorphism. The thermostabilities of polyurethanes 2,5-TDI/BP5 and 1,4-PDI/BP5 were measured at a heating rate of 1$0^{\circ}C$/min in air. The temperatures of 5% weight loss for 2,5-TDI/BP5 and 1,4-PDI/BP5 were 297 and 334$^{\circ}C$, respectively.

• 공업화학
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• 제8권2호
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• pp.339-346
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• 1997

액정 polyurethane은 DMF 용매중 1,4-bis(6-hydroxyhexoxy)benzene (BHB6)과 2,5-tolylene diisocyanate (2,5-TDI)를 중부가 반응에 의해서 합성하였다. 고유점도는 0.26, $0.42d{\ell}/g$였다. 생성된 polyurethane의 열적성질 및 구조확인은 DSC, 편광현미경, X-ray회절 그리고 $^1H$-NMR 및 FT-IR에 의해 확인하였다 특히 분자량이 서로 다른 polyurethane 2,5-TDI/BHB6의 열적성질 및 물성에 대해서 비교 검토하였다. 고유점도가 [${\eta}$]=0.26인 polyurethane 2,5-TDI/BHB6는 monotropic 액정성을 나타내었다. 이러한 것은 구조적으로는 mesogen을 포함하고 있지 않다. 예를 들면 LCPU-L(저분자량)은 $T_{I-LC}$(등방성액체상전이점-액정) 및 $T_{LC-K}$(액정-결정)은 $122^{\circ}C$부터 $89^{\circ}C$까지 관찰되었다.

• 한국막학회:학술대회논문집
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• 한국막학회 1996년도 춘계 총회 및 학술발표회
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• pp.30-32
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• 1996

Although the transport of small molecules through polymer membranes has been extensively studied for a long time, understanding of the transport mechanism is still far from satisfactory. This in turn makes difflcult the search for new membrane materials with the desired transport characteristics. Therefore it is of the utmost interest to study the correlations between a polymer's structure and morphology and its transport properties. Generally, polyurethanes serve as excellent polymer materials for such studies since their physical and chemical properties can be widely and systematically modified by varying the length, composition and chemical structure of the hard and soft segments. In this paper liquid crystalline polyurethanes are presented as new membrane materials for liquld separation and their transport properties with respect to molecular and supermolecular-structure are discussed.

• Bulletin of the Korean Chemical Society
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• 제22권7호
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• pp.753-757
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• 2001

1-(2'2'3'-Tricyano-3-carbomethoxycyclopropyl)-34-di-(2'-hydroxyethoxy)benzene, (4) was prepared by the reaction of bromomalononitrile with methyl 3,4-di-(2'-hydroxyethoxy)benzylidenecyanoacetate (3). Diol 4 was condensed with tolylene-2,4-diisocyanate, 3,3'-dimethoxy-4,4'-biphenylenediisocyanate, and 1,6-hexamethylenediisocyanate to yield polyurethanes 5, 6, and 7 containing tricyanocyclopropane functionalities in the pendant group. The resulting polymers 5-7 were soluble in common organic solvents and the inherent viscosities were in the range of 0.25-0.30 dL/g. Polyurethanes 5-7 showed a thermal stability up to 300 $^{\circ}C$ in TGA thermograms. Solution-cast films showed Tg values in the range of 100-125 $^{\circ}C$ and piezoelectric coeffcients (d31) of the poled polymer films were 1.3-2.0 pC/N, which are acceptable for piezoelectric device applications.

• 한국염색가공학회지
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• 제5권3호
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• pp.188-193
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• 1993

Aqueous polyurethanes(APU) were prepared from polypropylene glycol(PPG), dimethylol propionic acid(DMPA), and isophoron diisocyanate(IPDI) following a prepolymer mixing process. APUs were applied as binder for nonwoven fabrics processing. APU treated nonwoven fabrics generally showed better tear and tensile strength as compared with the untreated ones. In addition, depending on the soft segment length and crosslinking density of the PU, tear strength of APU treated fabrics was favorably compared with solvent type treated one. Similar results were obtained with microfiber nonwoven fabrics, however, the effect was less significant.

• 한국고분자학회:학술대회논문집
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• 한국고분자학회 2006년도 IUPAC International Symposium on Advanced Polymers for Emerging Technologies
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• pp.212-212
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• 2006

Polyurethane wastes can be depolymerized with glycols and/or amines. The depolymerization products may be recycled for the preparation of various polyurethanes. Caprolactam was employed to depolymerize Spandex fibers and the depolymerization products were evaluated as raw materials for the preparation of polyurethane elastomers. The depolymerization products were homogeneous and could be used to prepare polyurethane elastomers acceptable for various applications as binders.

• 한국섬유공학회:학술대회논문집
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• 한국섬유공학회 1998년도 가을 학술발표회논문집
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• pp.66-69
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• 1998

Most segmented polyurethanes are prepared from a two-step method where the polyol is end-capped with an excess of diisocyanate, followed by chain extension with stoichiometric amount of chain extender, In the final polymer the hard and soft segments tend to segregate, due to thermodynamic immiscibility and the differences in chemical structure between hard and soft segments, and produce a phase separated morphology of hard segment-rich and soft segment-rich phase. (omitted)

• 고무기술
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• 제8권2호
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• pp.116-128
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• 2007

• 대한화학회지
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• 제50권3호
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• pp.196-202
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• 2006

점탄성 용융 폴리우레탄의 자체확산분포가 완화스펙트럼과 자체확산분포 관계식으로부터 얻어졌다. ester, PCL PCL dyed 형의 용융 폴리우레탄의 완화스펙트럼은 실험적인 응력완화 곡선을 Ree-Eyring and Maxwell non-Newtonian model(REM 모델)이론식에 적용시켜서 얻는다. 용융폴리우레탄의 응력완화 실험은 온도조절 장치가 있는 physica 레오메타를 이용하여 여러 온도에서 수행되었다. 이론적인 완화스펙트럼은 REM model로부터 유도한 이론적인 완화스펙트럼식을 프로그램화한 컴퓨터 계산에서 구하였다. 폴리우레탄 시료의 자체확산과 비결정 영역의 홀거리가 응력완화 실험에 의해서 연구 조사되었다. 비결정 영역에서의 유동단위의 확산을 연구하기 위해서 확산계수와 홀부피가 유변학적인 파라메타와 결정크기로부터 계산되었다. 폴리우레탄 시료의 완화스펙트럼과 자체확산은 유동 단위의 분자량분포, 점도, 홀부피, 활성화에너지와 밀접한 관계가 있는 것을 알 수 있다.