• 폴리머
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• 제37권1호
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• pp.80-85
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• 2013

Hexafluoropropylene(HFP) dimer와 trimer로 구성된 올리고머의 조성비, 반응온도 그리고 hexafluoropropylene oxide(HFPO) 투입속도가 HFPO 음이온 중합반응에 미치는 영향 등을 알아보았다. HFP 올리고머는 불화금속 CsF와 TG를 사용한 음이온 반응을 통해 합성하였고, CsF 5 g, TG 10 g 그리고 반응온도 $0^{\circ}C$에서 합성된 HFP 올리고머의 dimer 함량은 상대적으로 높은 35.1%를 나타내었다. HFPO 음이온 중합의 경우, 반응온도 $0^{\circ}C$, HFP dimer 35.1%를 포함하고 있는 올리고머와 HFPO 투입속도 1.85 g/min에서 Cs(HFPO)n 알콕사이드는 상대적으로 원활한 사슬성장을 하면서 중량평균 분자량 3600을 나타내었다. 반면, 반응온도 $10^{\circ}C$ 및 증가된 HFPO 투입속도에서는 알콕사이드의 $F^{{\delta}-}$의 이탈현상을 촉진시켜 중평균 분자량은 감소되었다. 결론적으로, HFP 올리고머를 용매로 사용한 HFPO 음이온 중합반응의 사슬성장 및 사슬전이는 용매의 조성, 반응온도 및 단량체의 투입속도에 영향을 받고 있음을 알 수 있었다.

• 공업화학
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• 제35권4호
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• pp.296-302
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• 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.

• 한국세라믹학회지
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• 제36권2호
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• pp.220-224
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• 1999

질화규소 겔케스팅 공정제어를 위하여, MeOH의 첨가가 겔화유도시간과 성형체의 건조속도 및 기계적 특성에 미치는 영향에 대하여 조사하였다. 그 결과, 10~20 vol%의 MeOH 첨가에서 겉보기 겔화유도시간은 가장 크게 나타났으며, 이때의 건조속도는 약 25~40%의 증진효과를 나타내었다. 분산매에 대하여 40% MeOH 첨가 범위에서 성형체의 기계적 가공은 가능하였으나, 겔캐스팅 성형체의 상대밀도 및 강도는 다소 낮아졌다.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 1993년도 춘계학술대회 논문집
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• pp.28-32
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• 1993

A deposition rate of styrene thin films is linearly increased, but one of benzene thin films is nonlinearly increased with increasing discharge power under maintaining a polymerization time, pressure and monomer flow rate. And, the reduction of transmittance at shortwave is larger than that of transmittance at longwave. The refractive index with wavelength is various from 1.55 to 1.65. The refractive index of their thin films is decreased with increasing discharge power. Also, it is known that measured results are valid because the calculation of the extinction coefficient is about $10^3$ within variation of refractive index.

• Fibers and Polymers
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• 제2권2호
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• pp.75-80
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• 2001

The thermal degradation of poly(ethylene terephthalate-co-isophthalate)s (PETIs) is investigated by using isothermal thermogravimetric analysis at the temperature range of 280-31$0^{\circ}C$. The degradation rate of PETIs is increased as the mole ratio of ethylene isophthaloyl (EI) units in PETIs increases. The activation energies for the thermal degradation of poly(ethylene terephthalate), PETI(5/5), and poly(ethylene isophthalate) are 33.4, 16.6, and 8.9 kcal/mole, respectively. The degradation rate of PETIs is influenced by their volatile cyclic oligomer components formed during the polymerization and the thermal degradation. It is simulated by the rotational isomeric state model that the content of cyclic dimer in PETIs, which is the most volatile cyclic oligomer component, increases with the EI units in PETIs.

• Elastomers and Composites
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• 제51권2호
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• pp.99-105
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• 2016

Alkoxy modified silicone (PAMS) was synthesized from hydroxyl-terminated polydimethylsiloxane (OH-PDMS) and vinyltrimethoxysilane (VTMO) under alkali catalyst (NaOH and KOH) at room temperature ($25^{\circ}C$) via condensation polymerization. Then, the structural verification of the synthesized PAMS was confirmed using $^1H$-NMR and FT-IR spectroscopy. The reaction rate of PAMSs was studied in terms of the concentration variation of alkali catalyst. The reaction rate increased with the concentration of alkali catalyst, but no correlation between conversion and concentration of alkali catalyst was observed.

• Macromolecular Research
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• 제13권1호
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• pp.68-72
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• 2005

A low-molecular-weight poly(lactic acid) was synthesized through the condensation reaction of L-lactic acid. The effects that the catalyst and temperature have on the reaction rate were studied to determine the optimum reaction conditions. The reaction kinetics increased with temperature up to $210^{\circ}C$, but no further increase was observed above this temperature. Among a few selective catalysts, sulfuric acid was the most effective because it maximized the polymerization reaction rate. Reduction of the pressure was another important factor that enhanced this reactions kinetics.

• Journal of Pharmaceutical Investigation
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• 제21권2호
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• pp.111-116
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• 1991

Dextromethorphan HBr (DMP HBr) ion exchange albumin microcapsules were prepared by the interfacial polymerization method. The incorporation of drugs in empty albumin microcapsules was more increased in case of glutaraldehyde (GA) and formaldehyde (FA) than terephthaloyl chloride (TC) as a cross linking agent. The amount of DMP HBr incorporated into empty albumin micorcapsules was augemented with increasing DMP HBr concentration and the amount of empty microcapsules in the incorporation medium. Increasing the salt concentration in the release medium, the release rate and the DMP HBr amount released from microcapsules were increased. The release rates of DMP HBr from microcapsules retarded considerably compared with DMP HBr powder.

• 대한전기학회:학술대회논문집
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• 대한전기학회 1993년도 하계학술대회 논문집 B
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• pp.1189-1192
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• 1993

Organic thin films were fabricated an using interelectrode capacitively coupled type plasma polymerizaion apparatus, and their optical properties were investigated. A deposition rate of styrene thin films is linearly increased, but one or vinyl-pyridine thin films is nonlinearly increased with increasing of polymerization time, pressure and monomer flow rate. The transmittance of single layer thin films is constant, but that of multi-layer appeared irregular peak with increasing of the number of layers. And then the refractive index of organic thin films is various from 1.55 to 1.65 with wavelength, the extinction coefficient indicated $10^{-3}$.

• Journal of the Korean Wood Science and Technology
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• 제2권3호
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• pp.3-16
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• 1974

One of the disadvantages of. wood and wood products is their hydroscopicity or dimensional instability. This is responsible for the loss of green volume of lumber as seasoning degrade. Dimensional stabilization is needed to substantially reduce seasoning defects and degrades and for increasing the serviceability of wood products. Recently, considerable world-wide attention has been drawn to the so-called Wood-Plastic Composites by irradiation-and heat-catalyst-polymerization methods and many research and developmental works have been reported. Wood-Plastic Composites are the new products having the superior mechanical and physical properties and the combinated characteristics of wood and plastic. The purpose of this experiment was to obtain the basic data for the improvement of wooden materials by manufacturing WPC. The species examined were Mulpurae-Namoo (Fraxinus, rhynchophylla), Sea-Namoo (Carpinus laxiflora), Cheungcheung-Namoo (Cornus controversa), Gorosae-Namoo (Acermono), Karae-Namoo(Juglans mandshurica) and Sanbud-Namoo (Prunus sargentii), used as blocks of type A ($3{\times}3{\times}40cm$) and type B ($5{\times}5{\times}60cm$), and were conditioned to about 10~11% moisture content before impregnation in materials humidity control room. Methyl methacrylate (MMA) as monomer and benzoyl peroxide (BPO) as initiator are used. The monomer containing BPO was impregnated into wood pieces in the vacuum system. After impregnation, the treated samples were polymerized with heat-catalyst methods. The immersed weights of monomer in woods are directly proportionated to the impregnation times. Monomer impregnation properties of Cheungcheung-Namoo, Mulpurae-Namoo and Seo-Namoo are relatively good, but in Karae-Namoo, it is very difficult to impregnate the monomer MMA. Fig. 3 shows the linear relation between polymer retentions in wood and polymerization times; that is, the polymer loadings are increasing with polymerization times. Furthermore species, moisture content, specific gravity and anatomical or conductible structure of wood, bulking solvents and monomers etc have effects on both of impregnation of monomer and polymer retention. Physical properties of treated materials are shown in table 3. Increasing rates of specific gravity are ranged 3 to 24% and volume swelling 3 to 10%. ASE is 20 to 46%, AE 14 to 50% and RWA 18 to 40%. Especially, the ASE in relation to absorption of liquid water increases approximately with increase of polymer content, although the bulking effect of the polymerization of monomer may also be influential. WPCs from Mulpurae-Namoo and Cheungcheung-Namoo have high dimensional stability, while its of Karae-Namoo and Seo-Namoo are-very low. Table 4 shows the mechanical properties of WPCs from 6 species. With its specific gravity and polymer loading increase, all mechanical properties are on the increase. Increasing rate of bending strength is 10 to 40%, compression strength 25 to 70%, ;impact bending absorbed energy 4 to 74% and tensile strength 18 to 56%. Mulpurae-Namoo and Cheungcheung-Namoo with high polymer content have considerable high increasing rate of strengths. But incase of Karae-Namoo with inferior monomer impregnation it is very low. Polymer retention in cell wall is 0.32 to 0.70%. Most of the polymer is accumulated in cell lumen. Effective. of polymer retention is 58.59% for Mulpurae-Namoo, 26.27% for Seo-Namoo, 47.98% for Cheungcheung-Namoo, 25.64% for Korosae-Namoo, 9.96% for Karae-Namoo and 25.84% for Sanbud-Namoo.