• Title/Summary/Keyword: Polarizing microscope

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Orientational deformation of ferroelectric liquid crystal molecules by bending performance of plastic substrate

  • Son, Ock-Soo;Lee, Ji-Hoon;Jang, Chi-Woong;Lim, Tong-Kun
    • 한국정보디스플레이학회:학술대회논문집
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    • 2005.07a
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    • pp.338-341
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    • 2005
  • We have examined the aspects of the orientational ordering deformation of ferroelectric liquid crystal during bending performance of plastic substrate by analyzing the polarizing optical microscope texture and the birefringence of the cell. Striped texture becomes more prominent as the radius of curvature of substrate gets smaller. The optic axis of the adjacent stripes domain was not same and the relative angle between them becomes larger as the radius of curvature gets smaller. Especially, the optic axis rotation angle of one domain was lager than the other and the liquid crystal molecules in each domain became more coherent. In addition, the birefringence data with obliquely incident light shows the polar direction shift of liquid crystal molecule by bending performance.

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Synthesis and Physical Properties of Cholesteryl Biphenyl Ester Derivatives (Cholesteryl biphenyl erter계 액정의 합성 및 물성에 관한 연구)

  • Jeon, Yeong-Jae
    • Korean Journal of Materials Research
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    • v.3 no.3
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    • pp.223-229
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    • 1993
  • A homologous series of cholesteryl biphenyl ester derivatives was prepared. The thermal behaviors of compounds were studied by differential scanning calorimetry and by polarizing microscope equipped with a hot-stage. The cholesteric phase is present in all the compounds, whereas the smectic one is absent in the compounds with R = 1 and 2. The compounds possessed higher phase transitiof' temperature and wider temperature range of meso phase in comparison with known cholesteric liquid crystal phases.

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Synthesis and Properties of Thermotropic Compounds with Two Terminal Mesogenic Units and a Central Spacer (Ⅵ). Homologous Series of $\alpha,\;\omega$-Bis[4-(p-substituted benzoyloxy)benzoyloxy]alkanes$^*$

  • Jin, Jung-Il;Seong, Churl-Min;Jo Byung-Wook
    • Bulletin of the Korean Chemical Society
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    • v.6 no.1
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    • pp.40-45
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    • 1985
  • The thermal and optical properties of two new series of thermotropic, liquid crystalline compounds were studied by differential scanning calorimetry and on the hot-stage of a polarizing microscope. The first series contained two identical mesogenic units, 4-(p-phenylbenzoyloxy) benzoate moieties, at both ends of the polymethylene spacer of varying lengths and the second series, mesogenic units with different substituents and the hexamethylene group as the central spacer. A thermodynamic analysis of the phase transitions of the compounds was made and the results were discussed in relation to their chemical structures.

Synthesis and Properties of Thermotropic Compounds with Two Terminal Mesogenic Units and a Central Spacer (Ⅱ). Homologous Series of $\alpha,\;\omega$-Bis (4-p-substituted phenoxycarbonyl)phenoxyalkanes

  • Jin, Jung-Il;Chung, Yong-Seog;Lenz, R.W.;Ober, C.
    • Bulletin of the Korean Chemical Society
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    • v.4 no.3
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    • pp.143-148
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    • 1983
  • Two series of thermotropic compounds were prepared and their thermal and liquid crystal properties were examined by differential scanning calorimetry and on the hot-stage of a cross-polarizing microscope. The first series of the compounds has two terminal mesogenic units based on unsubstituted and substituted p-(phenoxycarbonyl) phenyl ethers bracketing a central decamethylene spacer, and the second has 4-(p-phenylphenoxycarbonyl) phenyl ether moiety as the two terminal mesogenic units and central polymethylene spacers of varying lengths. A thermodynamic analysis of the phase transitions was made and explained in relation to structures and thermotropic behavior of the compounds.

Dimesogenic Compounds Consisting of Two Identical Terminal N-(4-Oxybenzylidene)-4-n-butylaniline Units and a Central Polymethylene Spacer

  • Jung-Il Jin;Bong Young Chung;Joo-Hoon Park
    • Bulletin of the Korean Chemical Society
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    • v.12 no.5
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    • pp.583-588
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    • 1991
  • A series of dimesogenic compounds having two identical, terminal Schiff base type mesogens and a central polymethylene spacer were prepared and their properties were compared with those of the corresponding monomesogenic compounds. The mesomorphic properties of the compounds were studied by differential scanning calorimetry and on a hot-stage of a polarizing microscope. All of the dimesogenic compounds formed mesophases enantiotropically with the exception of pentamethylene-1,5-bis(4-oxybenzylidene 4-n-butylaniline). This compound was monotropic and formed only a nematic phase on heating the solid, whereas it formed nematic as well as smectic A phases on cooling the isotropic liquid. Those compounds containing longer (octamethylene and decamethylene) spacers favored the formation of nematic phase whereas those having shorter (dimethylene and tetramethylene) spacers formed smectic phases. In general, the variety of mesophase forms exhibited by the dimesogenic compounds was significantly less than that shown by the corresponding monomesogenic compounds.

Domain formation characteristics during thermomagnetic recording for amorphous TbFe and TbFeCo alloy thin films

  • Kim, Soon-Gwang
    • Proceedings of the Optical Society of Korea Conference
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    • 1989.02a
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    • pp.235-241
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    • 1989
  • Static according tests were carried out on a series of amorphous TbFe thin films of various composition under a constant laser irradiation condition. Examination of recorded domain configurations by using polarizing microscope led to the categorization of domain characteristics into 3 distinctly different types; i.c., type A: circular domains with smooth boundaries, the size not sensitive to variation of bias field, type B: domains of irregular shape at low bias, the size increasing and the boundaries getting smoother and more circular with increasing bias field and type C: not recordable. Critical factor which distinguishes among each types was fond to be the relative magnitude of H and H of the film near T, regardless of constituent atomic species. Micromagnetical process of thermomagnetic recording cycle was analyzed scheniatically for each type.

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The Formulation of Semi-Transparent Gel Emulsion by the Liquid Crystal Emulsification Method

  • Kim, Jungil;Lee, Youngkeun;Kim, Yongmin;Yun, Seiyoung
    • Journal of the Korean Applied Science and Technology
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    • v.35 no.4
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    • pp.1478-1486
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    • 2018
  • Liquid crystals offer plenty of useful activities as improving the stability of emulsion, increasing moisturizing power, drug release, improving skin feeling and visual effect for cosmetics fields. In order to prepare stable semi-transparent gel emulsion, liquid crystal emulsification method was used. The emulsion stabilities of systems containing glycerin, fatty alcohols, surfactants, water and oil were investigated at various temperatures as time passed. The stabilities of all emulsions were evaluated by means of a polarizing microscope, SEM, rheometer, colorimeter and DSC. Even though the samples stored at $50^{\circ}C$ thermostatic chamber were occurred the reduction of hardness, turbidity and ${\Delta}H$ and the peak shift, the semi-transparent gel emulsion was very stable without separation between water and oils phase in emulsion.

Synthesis and Liquid Crystalline Properties of Dimesogenic Compounds Containing Trifluoromethyl Substituents at Terminal Phenylene Rings and Central Decamethylene Spacer

  • Jo, Byung-Wook;Choi, Jae-Kon;Jin, Jung-Il;Chung, Bong-Yong
    • Bulletin of the Korean Chemical Society
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    • v.11 no.4
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    • pp.333-339
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    • 1990
  • A series of new dimesogenic compounds whose mesogens are of aromatic ester or amide type having a trifluoromethyl $(CF_3)$ substituent at the para-position of each terminal phenolic rings were prepared and their liquid crystalline properties were studied by differential scanning calorimetry (DSC) and on a cross-polarizing microscope. The compounds have two identical mesogenic units bracketing a central decamethylene spacer. Trifluoromethyl group appears to favor the formation of smectic phases when it is attached to a phenoxy or anilide terminal. Its group efficiency for mesophase formation seems to be inferior to other common substituents. A thermodynamic analysis of the phase transitions was made and the results were explained in relation to the structures of the compounds.

Thermotropic Compounds with Two Terminal Mesogenic Units and a Central Spacer, 8. Mutual Miscibility between the Dimesogenic, Nematic Compounds

  • Jin, Jung-Il;Choi, E-Joon;Park, Joo-Hoon
    • Bulletin of the Korean Chemical Society
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    • v.7 no.5
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    • pp.353-357
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    • 1986
  • Mutual miscibility between thermotropic, nematic compounds with two terminal mesogenic units and a central spacer was studied by differential scanning calorimetry (DSC) and on a polarizing microscope. It was found that the isomorphous, nematic dimesogenic compounds with wide variety of structures are miscible in mesophases with each other over the whole range of composition and that Schroder-van Laar equation almost correctly predicts the melting temperature and composition of eutectic mixtures. There was a pair of compounds which were exceptional and did not form a eutectic mixture and, instead, revealed a monotonous change in melting (T$_{m}$) and isotropic transition temperatures (T$_{i}$) as the composition of the mixture was varied. The compounds were of almost same structure in shape and seemed to undergo formation of solid solution.

A Study on the Synthesis and Functional Properties of the Thermotropic Polyurethanes (Thermotropic Polyurethanes의 合成과 機能性에 관한 硏究)

  • Lee, Jong Back;Song, Jin Cherl;Choi, Dae Woong
    • Textile Coloration and Finishing
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    • v.8 no.2
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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.

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