• 한국응용과학기술학회지
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• 제21권1호
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• pp.31-36
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• 2004

Liquid crystalline phases were formed from acylglutamate; polyglyceryl-10 myristate and glycerine mixture and they were used as a base material for preparing an O/W emulsion. When an oil phase is added into the liquid crystalline phases, it was inserted into the dispersed liquid crystal droplets rather than stayed outside the liquid crystals, which can be known by the fact that the size of liquid crystal droplets increases with the increasing oil phase content. Along with the increase in the droplet size, the complex modulus increases from 100 to 350 pascals and the loss angle decreases from 60 to 24 degrees, from which it can be known that the increase in the internal phase volume results in the increase in the elastic property of oil in liquid crystalline-phases (O/LC). When the water phase was lastly added into the O/LC phase, the emulsification occurred to form a O/W emulsion and the averaged particle size of the O/W emulsion changes from 22.5nm to 538nm with the addition of water phase. The results from the droplet size measurements and stability tests under accelerated conditions such as high temperature show that the obtained O/W emulsion is very consistent with time.

• Bulletin of the Korean Chemical Society
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• 제28권2호
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• pp.193-199
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• 2007

Raman and fluorescence spectroscopies were employed to study the coil effects on the intermolecular structure of a rod-coil liquid crystalline (LC) oligomer, the esterification products of ethyl 4-[4'-oxy-4-biphenylcarbonyloxy]- 4'-biphenylcarboxylate with poly(propylene)oxides (PPO) (DP=12) and poly(ethylene oxide)s (PEO) (DP=12). Three different vibrational modes (carbonyl, aromatic C-H, and aromatic C=C) obtained from the Raman experiment at variable temperature indicate that PPO and PEO coils induce the hydrogen bonding in a different manner. Further information about the micro-environment around the mesogenic unit obtained by fluorescence excitation spectra of P12-4 (LC with PPO coil) and 12-4 (LC with PEO coil) suggests that the mesogenic unit of P12-4 is quite different from that of 12-4 in intermolecular structure. This study supports the results obtained only from Raman spectroscopy, providing more accurate information about the intermolecular structural changes of liquid crystalline polymers at a molecular level during the phase transitions.

• Elastomers and Composites
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• 제44권3호
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• pp.329-335
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• 2009

4종류의 새로운 형태의 열방성 액정폴리우레탄을 4,4'-Bis(5-hydroxypentoxy)biphenyl (BP5)와 2,6-tolylene diisocyanate (2,6-TDI), 2,5-tolylene diisocyanate (2,5-TDI), 및 2,4-tolylene diisocyanate (2,4-TDI), 1,4-phenylene diisocyanate (1,4-PDI) 의 중부가 반응에 의해 합성하였다. 단량체 BP5은 스멕틱상을 형성하였으며 1,4-PDI/BP5을 제외한 나머지 폴리우레탄에서는 모두 액정성을 나타내었다. 생성된 폴리우레탄의 구조는 FT-IR과 ^1H$ NMR 스펙트럼으로 확인하였고 열적 성질은 DSC와 편광현미경으로 관찰하였다.

• Bulletin of the Korean Chemical Society
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• 제21권1호
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• pp.110-117
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• 2000

A series of new liquid crystalline dimesogenic compounds with chiral tails was synthesized, and their thermal and liquid crystalline properties were studied. The chain length of the central polymethylene spacers (x) was varied from dimethylene (2) to decamethylene (12). These compounds were characterized by elemental analysis, IR and NMR spectroscopy, differential scanning calorimetry (DSC), and cross-polarizing microscopy. All compounds were found to be enantiotropically liquid crystalline, and the values of melting ($T_m$) and isotropization temperature ($T_i$) as well as enthalpy change (Δ$H_i$) and entropy change for isotropization (Δ$S_i$) decreased in a zig-zag fashion revealing the so-called odd-even effect as x increases. Their mesomorphic properties fall into three categories depending upon x; (a) compounds with x=2 and 4 formed two different mesophases, smectic and cholesteric phases in that order on heating, and vice versa on cooling, (b) compounds with x=3, 7, 8, 10 and 11 reversibly formed only the cholesteric phase, and (c) compounds with x=5, 6, 9 and 12 exhibited only a cholesteric phase on heating, whereas on cooling they formed two different mesophases, cholesteric and smectic phases, sequentially.

• 대한화장품학회지
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• 제45권1호
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• pp.1-7
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• 2019

본 연구는 세테아릴 알코올, 세틸 팔미테이트, 소르비탄 팔미테이트, 소르비탄 올리베이트, 세라마이드 등을 이용하여 제조한 액정에멀젼의 다층구조에 따른 강화된 계면막에 의해 제형의 안정성이 확보됨을 확인하였다. 편광 현미경을 통해 제형 내 몰타 크로스(maltese cross) 무늬를 확인하고, cryo-SEM을 이용하여 다층구조가 형성되었음을 확인하였다. 소각 X선 산란법(SAXS)을 이용하여 라멜라 구조 생성여부를 확인하였으며, 점도계를 이용하여 점도변화를 확인하고 정적 광 산란법(SLS)을 이용하여 입도 분포를 확인하여 액정에멀젼의 제형 안정성을 입증하였다.

• 공업화학
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• 제28권6호
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• pp.679-684
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• 2017

베시클 막을 유연하게 만드는 edge activator를 혼합하여 수화 액정형 베시클을 제조하고 niacinamide를 베시클 안에 포집시켰다. 제조 과정 중 액정 상 형성 및 액정의 열적 상전이 현상을 편광현미경과 시차주사 열량계(DSC)를 통해 살펴보았다. Sodium deoxycholate, lysolecithin, polysorbate 80 등의 edge activator를 첨가하면 수화 액정형 베시클 입자가 수십 나노 사이즈로 줄어들었다. 수화 액정형 베시클을 활용하여 niacinamide를 피부 침투시키면 수용액 상태로 도포했을 때보다 피부 침투된 niacinamide의 양이 크게 증가하는데, 10% sodium deoxycholate를 혼합한 베시클에서는 niacinamide 침투량이 4배 가까이 증가하였다. 이러한 결과로부터 edge activator를 베시클에 혼합하면 베시클의 피부 침투력이 향상됨을 알 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제19권8호
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• pp.885-888
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• 1998

• 폴리머
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• 제36권1호
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• pp.9-15
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• 2012

용융법을 이용해서 말단에 가교 반응이 가능한 메틸 말레이미드(methyl maleimide)기를 가진 전방향족 에스터 결합의 액정(liquid crystal, LC)을 합성하였고, 합성된 LC를 이용해서 적당한 열처리 과정을 통해 열경화성 액정(liquid crystalline thermoset, LCT) 필름을 제조하였다. 합성된 LC 및 LCT 필름은 FTIR(Fourier transform infrared) 분광기, WAXD(wide angle X-ray diffraction), DSC(differential scanning calorimetry), TGA(thermogravimetric analysis), TMA(thermomechanical analysis), 그리고 가열판이 장착된 편광 현미경으로 특성 분석을 하였다. 유리전이온도($T_g$)와 열팽창 계수는 주사슬 구조의 메소겐에 의해 강한 영향을 받는 것으로 확인되었고, $para$-로 치환된 비페닐구조를 가진 LCT 필름이 가장 좋은 열적 성질을 보여 주었다.

• 대한화학회지
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• 제48권6호
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• pp.599-608
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• 2004

유연격자와 메타크릴로일 기 사이에 도입된 벤젠 고리와 메소겐 구조의 말단에 연결된 키랄 중심을 갖는 새로운 두 계열의 메타크릴레이트 단량체를 합성하였다. 이 두 계열에서 유연격자와 메소겐 기의 길이 변화에 따른 액정형성에 대한 효과를 조사하였다. 첫 번째 계열의 화합물들은 합성과정에서 얻어진 중간물질이나 최종물질에서 액정성을 보이지 않았다. 그러나 두 번째 계열에서는 중간물질 뿐만아니라 최종물질에서도 액정성을 보였다.

• Korea-Australia Rheology Journal
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• 제15권3호
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• pp.109-115
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• 2003

Rheometry testing and the DSC measurement of five thermotropic liquid crystalline polymers (TLCP) have been carried out. The dynamic viscosities of the five TLCPs show a typical shear-thinning behaviour obeying the power-law with the power indices from 0.2 to 0.3. When these TLCPs are heated above the melting temperatures determined by the DSC measurements, the dynamic viscosities first rapidly decrease by 2～3 orders of magnitude then level off, finally increase gradually with the further increasing of temperature. The steady shearing exhibited the same behaviour as the dynamic shearing, but serious edge fracture of material slippage out of the plates occurred. The abnormal temperature dependence of the viscosities can be explained by the nematic-isotropic transition. By using the concept of activation energy, we propose a simple model which can fit the shear-thinning behaviour quite well and predict qualitatively correct temperature effects.