• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2002년도 하계학술대회 논문집
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• pp.424-426
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• 2002

The surface and volume resistivity in the polymers, PE(polyethylene) and PP(polypropylene) mixtures are tested and measured by the ASTM D257(KS M3015) standard. Humidity effects on surface and volume resistivity in two polymers have been studied qualitatively at room temperature. The results of resistivity in these polymers show that the values of surface resistivity (and volume resistivity) at the humidity of 90% are remarkably small compared with those at the humidity of 50%, independing on applied voltage. When we varied the humidity in two polymers, it was found to takes many hours to recover into original surface resistivity (and volume resistivity) of these polymers.

• 한국전기전자재료학회논문지
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• 제14권7호
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• pp.595-599
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• 2001

The mechanisms of pretilt angle generation for a nematic liquid cystal (NLC) using a photodimerization method with obliquely polarized UV exposure on the various new photo-crosslinkable polymer were studied. A good thermal stability of all the photo-crosslinkable polymers was obtained by thermogravimetric analysis (TGA) measurement until 450$\^{C}$. High pretilt angle of the NLC was observed by polarized UV exposure on the three kinds of the photo-crosslinkable polymers containing biphenyl(BP), decyl(de), and cholesteryl(chol) group, respectively. However, the low pretilt angle of the NLC was measured by obliquely polarized UV exposure on the two kinds of the photo-crosslinkable polymers containing fluorine and chalcone group. Consequently, the high NLC angle generated is attributable to the biphenyl and alkyl moieties, and photo-dimerized chalcone group of the photopolymer.

• Macromolecular Research
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• 제10권5호
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• pp.241-245
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• 2002

A new aromatic diamine monomer containing benzoxazole substituents was prepared by a multi-step synthesis starting from 1,4-dibromo-2,5-difluorobenzene. This bulky and disc-shaped monomer was polymerized with commercial dianhydride monomers to give several different poly(amic acid)s with their inherent viscosities in the range of 0.24-0.35 dL/g. The prepared polymers were soluble in typical polar aprotic solvents. Thermal imidization to the corresponding polyimides were investigated by using FT-IR, DSC and TGA.

• KSBB Journal
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• 제14권3호
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• pp.273-278
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• 1999

The molecularly imprinted polymers(MIPs) synthesized at various polymerization conditions were examined as ibuprofen receptors in terms of binding characteristics. The 4-vinylpyridine polymers had 1.2 times higher adsorption capability for (S)-(+)-ibuprofen than the methacrylic acid polymers. The methacrylic acid polymers synthesized by UV radiation had 1.9 times higher selectivity for (S)-(+)-ibuprofen compared to those by thermal initiation. Effects of various solvents for binding were also examined in this research. According to the Scatchard analysis, the (S)-(+)-ibuprofen artificial receptors had two different kinds of binding sites for (S)-(+)-ibuprofen while having only single kind of binding site for ketoprofen. The binding sites of (S)-(+)-ibuprofen, n were calculated as 4.3~4.9 $\mu$mol/g and the dissociation constants, $K_D$ were 0.68 mM for the specific binding.

• 한국광학회:학술대회논문집
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• 한국광학회 1995년도 광학 및 양자전자학 워크샵 논문집
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• pp.161-168
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• 1995

Nonlinear optical absorption in solid films of poly(3-octyl thiophene) (P3OT) sensitized with methanofullerene was inverstigated for wacelengths from 620 to 960nm. The nonlinear absorption is ehnanced over that in either of the component materials by more than two orders orders of magitude at 760nm. The large nonlinearity results from effient photoinduced interm olecular charge transfer from P3OT to methanofullerene, followed by absorption in the charge separated excited state. P3OT/fullerene films are promising as reverse saturable absorbers and the optical limiting performance is demonstrated at 760nm.

• Bulletin of the Korean Chemical Society
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• 제35권2호
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• pp.513-517
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• 2014

Two donor-acceptor-donor monomers such as 3,5-bis(4-bromophenyl)-1,2,4-oxadiazole (BOB) and 3,5-bis(5-bromothiophen-2-yl)-1,2,4-oxadiazole (TOT) incorporating electron transporting and hole blocking 1,2,4-oxadiazloe moiety were copolymerized with light emitting fluorene derivative via Suzuki polycondensation to afford two new polymers, PFBOB and PFTOT, respectively. The optical studies for polymers PFBOB and PFTOT revealed that the band gaps are 3.10 eV and 2.72 eV, respectively, and polymer PFBOB exhibited a deep-blue emission while polymer PFTOT showed blue emission in chloroform and as thin film. The photoluminescence quantum efficiencies (${\Phi}_f$) of polymers PFBOB and PFTOT in chloroform calculated against highly blue emitting 9,10-diphenylanthracene (DPA, ${\Phi}_f=0.90$) were 1.00 and 0.44, respectively.

• Macromolecular Research
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• 제16권4호
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• pp.360-366
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• 2008

Poly(dialkoxyphenylene 1,3,4-oxadiazole)s were conveniently synthesized to compare their material properties of solvent solubility, thermal stability and molecular alignment with respect to alkyl chain length and meta/para-phenylene structure. All prepared polymers exhibited good solubility in co-solvents containing various volume levels of chloroform to trifluoroacetic acid. Meta-polymers showed slightly better solubility than para-polymers. All polymers produced were thermally stable up to $320^{\circ}C$. Photoluminescence of polymer films was observed with blue light emission at around 450 nm. X-ray diffraction patterns of all polymers indicated that they were composed of stacked molecular sheets with the same layer-to-layer distance of $3.4\;{\AA}$. However, side chain-to-side chain and main chain-to-main distances within the layers increased with increasing alkyl chain lengths. The meta-polymer chains were separated more than the para-polymer chains.

• Journal of the Korean Wood Science and Technology
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• 제21권2호
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• pp.31-37
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• 1993

Composites of styrene polymers with woody fibers were prepared, and the effect of compatibilizers on their mechanical properties was evaluated. To improve the compatibility of wood fibers and the matrix polymers, styrene-maleic anhydride copolymer(SMA) and maleic anhydride-modified polymers were used as compatibilizers. As results, maleic anhydride-modified polystyrene and SMA were proved to improve the tensile strength of the molded composites, and also were evaluated as good compatibilizers for the wood fiber polystyrene composite. Cellulosic fiber (dissolving pulp) provided better reinforcement than lignocellulosic fiber(thermomechanical pulp). On the contrary in the case of the composite of wood fiber and acrylonitrile-butadiene styrene copolymer(ABS), SMA and maleic anhydride-modified acrylonitrile-butadiene-styrene copolymer(MABS) did not act as compatibilizers. However, MABS was evaluated as a good polymer matrix to make wood fiber reinforced composite. The tensile properties of the composites of wood fiber and MABS were superior than those of wood fiber-ABS composites.

• Bulletin of the Korean Chemical Society
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• 제16권9호
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• pp.845-850
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• 1995

A systematic method is presented to analyze the bandgaps of conjugated polymers in terms of geometrical relaxations and electronic effect of moieties using the equation of Eg=ΔEδr + ΔE1-4 + ΔEel. The relationship between ΔEδr and δr is derived from trans-PA and is transferred to other conjugated polymeric systems. By applying this method to heterocyclic polymers, very useful information is obtained to understand the evolution of bandgaps of PT, PPy and PF in connection with the chemical structures and electronic effect of the heteroatoms. We believe that this method is very helpful to understand the evolution of bandgaps of various conjugated polymers in connection with the chemical structures and electronic effect of moieties. Also, the method is expected to provide valuable information to design a small bandgap polymers.

• Bulletin of the Korean Chemical Society
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• 제16권5호
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• pp.443-449
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• 1995

N-(Isopropyloxycarbonyloxy)maleimide (iPOCMI) has been synthesized and polymerized to give both the homopolymer and copolymers with substituted styrenes. These polymers were readily deprotected by thermolysis of the isopropyloxycarbonyl (iPOC) groups to provide the corresponding N-hydroxymaleimide (HOMI) polymers. The homopolymer and styrenic copolymers of iPOCMI were radically obtained in higher conversion and higher molecular weight than those obtained by direct polymerizations of N-hydroxymaleimide. The homopolymer of iPOCMI was transformed into poly(N-hydroxymaleimide)P(HOMI) by thermolysis of iPOC groups at 205 $^{\circ}C$ with concurrent release of propene and carbon dioxide. The copolymer of iPOCMI and styrene was thermally deprotected to the copolymer of HOMI and styrene at 235 $^{\circ}C.$ The mass loss was 28% and the Tg of the resulting copolymer was 250 $^{\circ}C.$ The thermal deprotection readily provided the desired, polar HOMI polymers which have Tgs above 240 $^{\circ}C.$ The deprotection was accompanied by large changes in aqueous base solubility.