• 한국유변학회:학술대회논문집
• /
• 한국유변학회 2006년도 춘계 학술발표회 논문집
• /
• pp.187-190
• /
• 2006

• 공업화학
• /
• 제35권4호
• /
• pp.296-302
• /
• 2024

염화 철(III)을 이용한 2-에티닐피리딘의 in-situ 4차염화 중합을 통하여 이온성 폴리아세틸렌-염화 철(III) 복합체를 용이하게 합성하였다. 합성한 폴리아세틸렌-염화 철(III) 복합체의 구조를 여러 가지 분석장비를 통해 확인한 결과 설계한 염화 철(III)-피리디늄 치환기를 갖는 공액구조 고분자가 생성되었음을 확인할 수 있었다. 본 중합의 메커니즘은 첫 번째 단계에서 형성된 에티닐피리디늄 염의 중합반응이 개시되고 전파되는 것으로 분석되었다. P2EP-FeCl₃ 복합체의 전기 광학 및 전기화학적 특성을 연구하였다. P2EP-FeCl₃ 복합체의 UV-visible 스펙트럼에서 흡수 최대값은 480 nm 및 533 nm이었고 PL 최대값은 598 nm로 나타났다. P2EP-FeCl₃ 복합체의 순환 전압전류 특성 측정결과 산화 피크와 환원 피크가 비가역적인 전기화학적 거동을 보였으며, 복합체의 산화 환원 과정의 동역학은 스캔 속도 대비 산화 전류 값의 도표부터 확산 제어 프로세스에 가까운 것으로 확인되었다.

• 공업화학
• /
• 제27권1호
• /
• pp.45-49
• /
• 2016

과량의 GO 및 poly(4-styrene sulfonate) (PSS)의 존재 하에서 산화제 없이 3,4-ethylenedioxythiophene (EDOT)의 in-situ 중합 반응을 시도하였다. 반응물(GO-P)의 XPS, FT-IR 등의 분석을 통하여 산화제 없이도 모노머인 EDOT의 산화중합이 원활하게 진행되어 PEDOT/PSS가 합성되고 GO와 복합화된 것을 확인할 수 있었다. GO-P는 수분산성은 우수하였으나, 전기적 절연체인 GO가 42% 포함되어 있으므로 전기전도도는 $15S{\cdot}m^{-1}$로 매우 낮았다. 그러나 GO-P 필름을 $200^{\circ}C$에서 8 h 열처리하면 GO의 일부분이 환원되면서 전도도가 $212S{\cdot}m^{-1}$까지 향상되었다.

• Composites Research
• /
• 제32권6호
• /
• pp.375-381
• /
• 2019

Multiwalled carbon nanotubes (MWCNTs) are covalently functionalized with isocyanates by directly reacting commercial hydroxyl functionalized MWCNTs with excess 4,4'-methylenebis (phenyl isocyanate) (MDI) and hexamethylene diiosocyanate (HDI). HDI-modified MWCNTs results in a higher surface isocyanate density than MDI-modified MWCNTs. Anionic ring-opening polymerization of ε-caprolactam is conducted using a sodium caprolactam initiator in combination with a di-functional hexamethylene-1,6-dicarbamoylcaprolactam activator in the presence of isocyanate functionalized MWCNTs. This polymerization proceeds in a highly efficient manner at relatively low reaction temperature (150℃) and short reaction times (10 min). During the polymerization, the isocyanate functionalized MWCNTs act not only as reinforcing fillers but also as second activators. Nanocomposites with HDI modified MWCNTs exhibit higher reinforcement and faster isothermal crystallization than MDI modified MWCNTs. The results show that PA6 chains grow more effectively from HDI modified MWCNT surface than from MDI modified MWCNT surface, resulting in stronger interaction between PA6 and MWCNTs.

• Bulletin of the Korean Chemical Society
• /
• 제33권7호
• /
• pp.2345-2351
• /
• 2012

Conductive honeycomb-patterned polystyrene (PS) thin films were prepared by the formation of a polyaniline (PANI) thin layer on the surface of the patterned PS thin films using simple one-step chemical oxidative polymerization of aniline. The in situ chemical oxidation polymerization of aniline hydrochloride solution on the patterned structure of the PS films was conducted in the presence of multiwalled carbon nanotubes (MWCNT) to prepare the PANI-MWCNT/PS composite film. The concentration (wt %) of MWCNT was varied in the range of 1%-3% by weight. The dependence of surface morphology of the PANI/PS and PANI-MWCNT/PS composite film to the polymerization time was observed by scanning electron microscopy. The room temperature DC conductivity was obtained by the four-probe technique. The conductivity of the PANI-MWCNT/PS composite film was affected both by the MWCNT concentration and polymerization time. In addition, DC electrical field was loaded during the oxidative polymerization to affect the distribution of the MWCNT included in the composite film, varying the loading voltage in the range of 0.1-3.0 V. The conductivity of the PANI-MWCNT/PS composite film was increased as loading voltage rose. However, this increase stops at a voltage higher than the critical value.

• Fibers and Polymers
• /
• 제5권4호
• /
• pp.253-258
• /
• 2004

Living nature of photoinduced cationic polymerization of isobutyl vinyl ether (IBVE) in the presence of various combinations of diphenyliodonium halide (DPIX), a photocationic initiator and zinc halide $(ZnX_2)$ in methylene chloride has been investigated. Attainment of $100\%$ conversion and a linear relationship between $\%$conversion and number average molar mass of the resulting polymer, strongly suggests the living nature of this system. Livingness of the polymerization system was observed irrespective to the type of halide anion of the initiator and zinc salts unless the reaction temperature is not higher than $-30^{\circ}C$. The rate of polymerization decreases in the order of iodide > bromide > chloride when halide salt of DPIX and $ZnX_2$ are used. It is postulated that the cationic initiation is started by the insertion of weakly basic monomer in to the activated C-X terminal of the monomer adduct which is a reaction product of monomer and HX, a photolytic product of DPIX, formed in situ during the photo-irradiation process. It was concluded that polymerization is initiated by the insertion of weakly basic monomer into activated C- X terminal of monomer adduct due to the pulling action of$ZnX_2$, which successively producing a new polarized C-X terminal for the propagation in cationic nature. This led us to a conclusion that the living nature of this cationic polymerization is ascribable to the polarized C-X growing terminal, which is stable enough to depress the processes of chain transfer or termination process.

• Bulletin of the Korean Chemical Society
• /
• 제35권1호
• /
• pp.236-242
• /
• 2014

Isospecific propylene polymerization behavior of meta- and para-Lewis base (E) functionalized unbridged zirconocenes ($[1-(E_n-Ph)-3,4-Me_2C_5H_2]_2ZrCl_2$, E = $NMe_2$, OMe; n = 1 or 2) was investigated under bulk conditions. Catalytic activity of the zirconocenes, and molecular weight and isotacticity of polypropylenes are found to be dependent on the position and number of the Lewis base functional groups in the zirconocenes. All the crude polypropylenes possess a broad molecular weight distribution and multi-melting transitions, indicating an involvement of multi-catalytic active species in the polymerization. The highest [mmmm] value of an isotactic portion of the polypropylenes reached 89%, which is higher than that (85%) from the well-known $C_2$-symmetric EBIZr (rac-$Et(Ind)_2ZrCl_2$) catalyst. These results support that the in situ generated, rigid rac-like cation-anion pair through the Lewis acid-base interactions between the functional groups of zirconocenes and methylaluminoxane anion is effective in the formation of isotactic polypropylene under bulk propylene polymerization conditions.

• Macromolecular Research
• /
• 제13권2호
• /
• pp.102-106
• /
• 2005

Poly(methyl methacrylate) (PMMA)/sodium montmorillonite (Na-MMT) nanocomposites were prepared with a novel method utilizing a macroazoinitiator (MAI). To induce the intergallery polymerization of methyl methacrylate (MMA), the MAI containing a po1y(ethylene glycol) (PEG) segment was intercalated between the lamellae of Na-MMT and swelled with water to enhance the diffusion of MMA into the gallery. The structure of the nanocomposite was examined using X-ray diffraction and transmission electron microscopy, and the thermal properties were examined using differential scanning calorimetry and thermogravimetry. The PMMA/Na-MMT nanocomposite prepared by intergallery polymerization showed a distinct enhancement of its thermal properties; an approximately $30^{\circ}C$ increase in its glass transition temperature and an $80\sim100^{\circ}C$ increase in its thermal decomposition temperature for a $10\%$ weight loss.

• Bulletin of the Korean Chemical Society
• /
• 제31권5호
• /
• pp.1252-1256
• /
• 2010

A polyvinylpyrrolidone (PVP)/Ag nanocomposites was prepared by the simultaneous thermal reduction and radical polymerization route. The in situ synthesis of the Ag/PVP nanocomposites is based on the finding that the silver n-propylcarbamate (Ag-PCB) complex can be directly dissolved in the NVP monomer, and decomposed by only heat treatment in the range of 110 to $130^{\circ}C$ to form silver metal. Silver nanoparticles with a narrow size distribution (5 - 40 nm) were obtained, which were well dispersed in the PVP matrix. A successful synthesis of Ag/PVP nanocomposites then proceeded upon heat treatment as low as $110^{\circ}C$. Moreover, important advantages of the in situ synthesis of Ag/PVP composites include that no additives (e.g. solvent, surface-active agent, or reductant of metallic ions) are used, and that the stable silver nanocolloid solution can be directly prepared in high concentration simply by dissolving the Ag/PVP nanocomposites in water or organic solvent.

• Carbon letters
• /
• 제14권4호
• /
• pp.251-254
• /
• 2013

In this study, poly(amic acid) was prepared via a polycondensation reaction of 3,3'-dihydroxybenzidine and pyromellitic dianhydride in an N-methyl-2-pyrrolidone solution; reduced graphene oxide/polybenzoxazole (r-GO/PBO) composite films, which significantly increased the electrical conductivity, were successfully fabricated. GO was prepared from graphite using Brodie's method. The GO was used as nanofillers for the preparation of r-GO/PBO composites through an in situ polymerization. The addition of 50 wt% GO led to a significant increase in the electrical conductivity of the composite films by more than sixteen orders of magnitude compared with that of pure PBO films as a result of the electrical percolation networks in the r-GO during the thermal treatment at various temperatures within the films.