• Polymer Science and Technology
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• v.5 no.4
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• pp.353-366
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• 1994

• Polymer Science and Technology
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• v.5 no.3
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• pp.254-264
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• 1994

• The Korean Journal of Rheology
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• v.4 no.2
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• pp.99-106
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• 1992

전방향족 폴리에스테르계 열방성 액정중합체(Vectra A-950)를 대상으로 유로가 확 장되는 다이로의 압출을 통하여 액정 섬유상의 배향 특성을 조사하고 이들이 기계적 특성에 미치는 영향을 살펴보았다, 다이의 확장 효과에 의하여 중심에서는 유동방향과 수직방향으 로 섬유상이 이중 배향되었으며 가장자리에서는 주로 유동방향으로만 배향이 일어났다. 그 리고 배향 특성은 두께방향으로 상하 대칭성을 갖는 바깥 영역과 중간영역으로 구별되었으 며 겉층은 유동방향으로 배향되고 속층은 중심에서 멀어지면서 배향각이 점진적으로 달라졌 다. 이런한 시편의 기계적 강도는 압출다이의 확장각이 증가하거나 스크류 속도가 증가함으 로 따라 유동방향이나 그 수직방향 모두 현저한 증가를 보였으나 파단신도는 유동방향은 감 소하고 수직방향은 증가하여 증가하여 결과적으로 거의 비슷하였으며 파단신도가 배향상태 를 가장 잘 반영하는 기계적 특성임을 알 수 있었다.

• Applied Chemistry for Engineering
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• v.3 no.2
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• pp.280-287
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• 1992

Aromatic liquid crystalline polyesters were synthesized from terephthalic acid(TPA), biphenyl dicarboxylic acid(BPA) and hydroquinone(HQ) by solution polymerization. Effects of TPA/BPA ratio(by mole %) on the thermal properties, thermal stability and textures of mesophases were investigated with DSC, TGA, cross-polarized microscopy and X-ray diffractometer. The synthesized polymers in this study were thermotropic and showed nematic textures. Melting temperature($T_m$) and isotropization temperature($T_i$) of polymer increased and thermal stabilities of polymer were improved with the content of BPA. Most of the polymers in this study had crystallinity more than 30%.

• Journal of the Korean Chemical Society
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• v.50 no.3
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• pp.263-268
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• 2006

• Polymer(Korea)
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• v.33 no.4
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• pp.297-306
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• 2009

A homologous series of side chain liquid crystalline polymers, poly [1-{4-(4'-cyanophenylazo)phenoxyalkyloxy}ethylene]s(CAPETn, where n, the number of methylene units in the spacer, is $2{\sim}10$) were synthesized from poly(vinyl alcohol) and 1-{4-(4'-cyanophenylazo)phenoxy}alkylbromides(CAPBn, n=$2{\sim}10$), and their thermotropic liquid crystalline phase behaviors were investigated. The CAPBn with n of $2{\sim}5$ did not show any liquid crystalline behavior, while those with n of 6 and $7{\sim}10$ showed enantiotropic and monotropic nematic phases, respectively. In contrast, among the CAPETn polymers, only CAPET5 exhibited an enantiotropic nematic phase, while other polymers showed monotropic nematic phases. The isotropic-nematic transition temperatures of CAPETns and their entropy variation at the phase transition that were higher values than those of CAPBns, demonstrated a typical odd-even effect as a function of n. These phase transition behaviors were disscussed in terms of the 'virtual trimer model' by Imrie. The mesophase properties of CAPETns were largely different from those reported for the polymers in which the (cyanophenylazo) phenoxy groups are attached to polyacrylate, polymethacrylate, and polystyrene backbones through polymethylene spacers. The results indicate that the mode of chemical linkage of the side group with the main chain plays an important role in the formation, stabilization, and type of mesophase.

• Polymer(Korea)
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• v.36 no.3
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• pp.380-392
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• 2012

Four kinds of N,O-hydroxypropyl chitosans (HPCTOs) with degree of substitution(DS) and molar substitution (MS) ranging from 2.47 to 2.52 and 4.9 to 7.8, respectively were synthesized, and their molecular chracteristics and thermotropic and lyotropic liquid crystalline properties were investigated. MS was exceedingly larger than DS, showing that in the later stages of reaction, propylene oxide was preferentially added to the side chains rather than the main chain. All the derivatives formed thermotropic cholesteric phases. The glass and clearing temperatures were decreased with increasing MS. The optical pitches (${\lambda}_m$'s) of the thermotropic cholesteric phases increased with temperature. However, the ${\lambda}_m$'s of the derivatives at the same temperature increased with increasing MS. Solutions of HPCTOs in water, methanol, ethanol, acetic acid, and formic acid containing more than 30 wt% polymer also formed cholesteic phases whose ${\lambda}_m$'s decreased exponentially with increasing polymer concentration. The concentration dependence of ${\lambda}_m$ of HPCTO solutions, however, highly depended on the nature of the solvent and MS. The thermotropic and lyotropic mesophase properties of HPCTOs were significantly different from those reported for hydroxypropyl celluloses. The results indicate that the secondary amino group in the C-2 position plays an important role on the formation, stabilization, and temperature and concentration dependencies of ${\lambda}_m$ of the cholesteric mesophase.

• Korean Journal of Materials Research
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• v.10 no.5
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• pp.350-353
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• 2000

Thermotropic liquid crystalline polymer(LCP) has been used for the alignment of ferroelectric liquid crystal (FLC) molecules and the surface morphology of the resulting polymeric thin film has been observed by atomic forced microscope. The uniform alignment of FLC molecules on the surface of thermotropic LCP thin film was obtained even though microgroove structures were not formed. The contrast ratio of sample cell was about 23:1 including two polarizers and a good memory capability due to the bistability of FLC was obtained. After AC field stabilization at 20V, the typical stripe-shaped patterns appeared.

• Polymer(Korea)
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• v.24 no.3
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• pp.418-430
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• 2000

A new hydroxylpropyl chitosan (HPCTO) capable of forming both thermotropic and lyotropic liquid crystalline phases was synthesized by reaction of alkali chitosan with propylene oxide and its solid films cross-linked with glyoxal were prepared by casting the liquid crystalline solution in methanol. The thermal and swelling properties of the cross-linked films were investigated. The films displayed fingerprint patterns characteristic of cholesteric liquid-crystalline phase, and their pitches increased with increasing temperature and cross-linker concentration. The cross-linked samples exhibited an anisotropic swelling in both water and methanol, suggesting that the two-dimensional cross-linking preferentially performs between HPCTO molecules. The degree of anisotropy highly depended on the solvent, but hardly on the cross-linker concentration investigated.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.11 no.12
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• pp.5216-5220
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• 2010

Rheological measurement of a thermotropic liquid crystalline poymer (TLCP) is not an easy task since their rheological responses are strongly influenced by a thermal history during a processing and thus the reproducibility of the measurement is poor. In order to find out a cause for the strong influence of the thermal history, rheological measurements and DSC observations of the TLCP having various thermal histories were carried out. It was observed that the TLCP used in this study shows liquid-like behavior at a temperature above a crystal-nematic transition temperature ($280^{\circ}C$), but at the same time crystallization can occur at this temperature range and as a consequence the viscosity of the polymer continuously increases. When the samples are heated beyond the $320^{\circ}C$, all crystals thus formed and the thermal histories were observed to disappear. Crystallization rate of the samples annealed above $320^{\circ}C$ was very low at even the lowed temperature ($280^{\circ}C\;{\sim}\;320^{\circ}C$). Therefore, it is concluded that rheological measurements of TLCP used in this study must be performed after annealed above the nematic-isotropic transition temperature for better reproducibility.