• 접착 및 계면
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• 제2권2호
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• pp.11-19
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• 2001

트리카프릴메틸 암모니움 클로라이드를 상이동촉매로 사용하여 $Na_2S_2O_8$의 수용액과 톨루엔의 이상계에서 질소분위기하에 $60^{\circ}C$에서 스티렌의 라디칼중합을 행하였다. 중합시의 초기 중합속도는 촉매와 $Na_2S_2O_8$의 초기공급 농도보다는 수용액 상에서의 4급 암모늄양이온과 퍼록시디슬페이트 음이온의 농도로 나타낼 수 있었다. 관찰된 초기중합속도를 사용하여 분균일 액-액계에서의 순환 상이동에 의한 개시과정을 포함한 중함메카니즘을 밝힐 수 있었다. 폴리스티렌의 점도평균분자량은 $Na_2S_2O_8$의 농도에 역비례하였는데, 라디칼 중합메카니즘에 의하여 $[Q^+]([S_2O{_8}^{2-}]{\alpha}_2)^{1/2}$로 나타내어졌다.

• Carbon letters
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• 제13권3호
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• pp.133-138
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• 2012

According to kinetic mechanisms, liquid phase polymerization and solid phase polymerization are different in acrylonitrile (AN) polymerization, and so the relationship between the contribution ratio and molecular weight distribution (MWD) was obtained through theoretic analysis. The precipitation homopolymerization of AN was carried out in a mixture solution of dimethyl sulfoxide (DMSO) and water at $50{\sim}65^{\circ}C$ using ${\alpha}$,${\alpha}^{\prime}$-azobisisobutyronitrile as an initiator. The contribution ratio decreased and approached 0; the MWD also decreased and approached 2 with the increase of the $H_2O$/DMSO ratio from 10/90 to 90/10. The experimental data were found to coincide well with the theoretical equation derived from the mechanisms.

• 한국인쇄학회지
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• 제18권1호
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• pp.13-24
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• 2000

UV-curable resin has the properties of quick-drying, high productivity at low temperature, energy, space saving, solventless, non-polluting and low-stinking, and thus, UV-curing system has been widely used in the fields of printing inks, adhesives, paints and coating agents. This study has been executed to develop a new functionnal material by the polymerization induced phase separation. The results obtained were as follows. As for the curing properties of the monomer/prepolymer/alkyd resin blends, it was found out that there was a peak by the polymerization induced phase separation when measuring the changes of viscosity and elasticity. It was also found out that such polymerization phase separation occurred in case that the alkyd resin contents were 20wt% and 30wt% and not found at the contents of 40wt%. Therefore, it would be desirable to maintain the contents of alkyd resin at less than 30wt% in order to use the polymerization induced phase separation.

• 한국염색가공학회지
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• 제15권3호
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• pp.127-131
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• 2003

Acrylonitrile(AN) was solution-polymerized in dimethyl sulfoxide(DMSO) and tertiary butyl alcohol(TBA) at 30, 40, $50^\circ{C}$ using a low temperature initiator, 2,2'-azobis(2,4-dimethylvaleronitrile) (ADMVN). The low temperature polymerization using ADMVN, DMSO, and TBA is to be successful in obtaining high molecular weight polyacrylonitrile(PAN) with less branches by solution polymerization. Throug a polymerization of AN in DMSO at $30^\circ{C}$, PAN having viscosity-average molecular weight$(M_v)$ of 931,000 was obtained. And then, during AN solution polymerization in DMSO and TBA using a cosolvent system the in-situ formation of microfibrillar structure has been discovered at the cosolvent composition of 24/1$(V_{DMSO}/V_{TBA})$. The simultaneous process of gelation and phase separation of long chain molecules may explain the in-situ formation of PAN fibers during polymerization.

• Structural Engineering and Mechanics
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• 제2권4호
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• pp.383-393
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• 1994

The residual stress distribution in a unidirectional graphite/epoxy laminate induced during the fabrication process is investigated at the microstress level within the scope of linear viscoelasticity. To estimate the residual stresses, the fabrication process is divided into polymerization phase and cool-down phase, and strength of materials approach is employed. Large residual stresses are not generated during polymerization phase because the relaxation modulus is relatively small due to the relaxation ability at this temperature level. The residual stresses increase remarkably during cool-down process. The magnitude of final residual stress is about 80% of the ultimate strength of the matrix material at room temperature. This suggests that the residual stress can have a significant effect on the performance of composite structure.

• Bulletin of the Korean Chemical Society
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• 제31권10호
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• pp.2943-2948
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• 2010

Silica monolith powders were prepared by a new procedure where ground powders of proper size distribution were obtained without sieving. An initiator was attached to this ground monolith and polystyrene was bound by reversible addition-fragmentation chain transfer polymerization to give a new stationary phase. The separation efficiency of this phase was found better than that of the polystyrene bound phase based on conventional silica particles and that of the C18 bound silica monolith powders.

• 공업화학
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• 제4권2호
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• pp.300-307
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• 1993

$Na_2S_2O_4$ 수용액과 $CCl_4$-toluene 용액의 2상에서 유기상에 용해하는 tricaprylmethylammonium chloride 상이동 촉매를 사용하여 methyl methacrylate의 라디칼 중합속도를 측정하여, 액-액 불균일계 접촉계면을 통한 라디칼 중합반응기구를 해석하였다. MMA의 중합속도는 수용액상에 존재하는 $Q^+$ 이온의 농도와 ${S_2O_4}^{-2}$ 이온의 농도의 제곱근에 정비례하고 $CCl_4$와 MMA의 농도에 각각 정비례하였다.

• Macromolecular Research
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• 제9권1호
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• pp.51-65
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• 2001

Two-stage emulsion polymerizations of hydrophobic monomers on hydrophilic seed polymer particles were carried out to make core-shell composite particles. It was found that the loci of polymerization in the second stage were the surface layer of the hydrophilic seed latex particles, and that it has resulted in the formation of either eccentric core-shell particles with the core exposed to the aqueous phase or aggregated nonspherical composite particles with the shell attached on the seed surface as many small separated particles. The driving force of these phenomena is related to the gain in free energy of the system in going from the hydrophobic polymer-water interface to hydrophilic polymer-water interface. Thermodynamic analysis of the present polymerization system, which was based on spreading coefficients, supported the likely occurrence of such nonspherical particles due to the combined effects of interfacial free energies and phase separation between the two polymer phases. A hypothetical pathway was proposed to prepare hydrophilic core-hydrophobic shell composite latex particles, which is based on the concept of opposing driving and resistance forces for the phase migration. It was found that the viscosity of the monomer-swollen polymer phase played important role in the formation of particle morphology.

• 폴리머
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• 제34권5호
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• pp.450-453
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• 2010

Iron(III) p-toluenesulfonate(FTS)를 개시제로 한 pyrrole의 중합에서 용액 중합법(LPP)과 기상 중합법(VPP)으로 제조된 PPy 박막의 전기/광학적 특성 및 표면구조를 비교하였다. LPP에 비해서 VPP 방법으로 제조된 PPy 박막은 우수한 전기적 특성을 보여주었다. 표면 특성분석을 이용하여 제조된 PPy 필름의 표면 모폴로지와 표면저항과의 상관관계를 검토하였다. VPP 방법으로 제조된 PPy 박막의 표면이 LPP로 제조된 것보다 평탄하였다. VPP를 응용한 잉크젯 프린팅과 소프트 리소그래피를 사용하여 미세 패턴된 PPy 박막을 효과적으로 제조할 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제27권10호
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• pp.1633-1637
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• 2006

We demonstrate a selective vapor-phase deposition of conductive poly(3,4-ethylenedioxythiophene) (PEDOT) thin films on patterned $FeCl_3$. The PEDOT thin films were grown on various substrates by using the vapor-phase polymerization of ethylenedioxythiophene (EDOT) with $FeCl_3$ catalytic layers at 325 K. The selective deposition of the PEDOT thin films using vapor-phase polymerization was accomplished with patterned $FeCl_3$ layers as templates. Microcontact printing was done to prepare patterned $FeCl_3$ on polyethyleneterephthalate (PET) substrates. The selective vapor-phase deposition is based on the fact that the PEDOT thin films are selectively deposited only on the regions exposing $FeCl_3$ of the PET substrates, because the EDOT monomer can be polymerized only in the presence of oxidants, such as $FeCl_3$, Fe($CIO_4$), and iron(II) salts of organic acids/inorganic acids containing organic radicals.