• 청정기술
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• 제17권3호
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• pp.244-249
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• 2011

이산화탄소/프로필렌 옥사이드 공중합을 통하여 고분자 사슬 내에 친수성기와 소수성기가 공존하는 저분자량의 블록 공중 합체를 합성하였다. 고활성의 촉매를 사용한 이산화탄소/프로필렌 옥사이드 공중합 반응에 단말기로 -OH기를 갖는 폴리(에틸렌 글리콜)(PEG)을 분자량 조절제로 투입하여 블록 공중합체를 합성하였다. 단말기 한쪽 끝에만 -OH기를 갖는 폴리(에틸렌 글리콜)을 투입하였을 때는 PEG-block-PPC (폴리(프로필렌 카보네이트)) 다이블록 공중합체가 얻어지고, 단말기 양쪽 끝 모두 -OH기를 갖는 폴리(에틸렌 글리콜)을 투입하였을 때는 PPC-block-PEG-block-PPC 트리블록 공중합체가 얻어진다. 제조된 블록 공중합체는 $^1H$-NMR 스펙트럼을 통하여 구조 분석을 하였고 GPC를 통하여 분자량을 측정하였다.

• Korean Chemical Engineering Research
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• 제57권1호
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• pp.73-77
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• 2019

Isothermal (vapor + liquid) equilibrium data measurements were undertaken for the binary mixtures of (propylene oxide + 1-pentanol) system at three different temperatures (303.15, 318.15, and 333.15) K. The Peng-Robinson-Stryjek-Vera equation of state (PRSV EOS) was used to correlate the experimental data. The van der Waals one-fluid mixing rule was used for the vapor phase and the Wong-Sandler mixing rule, which incorporates the non-random two liquid (NRTL) model, the universal quasi-chemical (UNIQUAC) model and the Wilson model, was used for the liquid phase. The experimental data were in good agreement with the correlation results.

• Korean Chemical Engineering Research
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• 제44권2호
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• pp.121-128
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• 2006

티타늄 함유 제올라이트 촉매 TS-1과 Ti-MCM-22를 이용하여 과산화수소를 산화제로 한 프로필렌 에폭시화반응을 수행하였으며, 반응에 미치는 촉매량, 한계 반응물인 과산화수소의 양, 교반 속도, 반응 온도, 압력, 용매 및 생성물 억제 효과를 조사하였다. TS-1은 우수한 부분 산화반응 촉매로 표준 반응조건($45^{\circ}C$, 7 atm, 0.5 g catalyst, 2.5 wt％ $H_2O_2$, 메탄올 용매, 1,000 rpm 교반)에서 95％ 이상의 $H_2O_2$ 전화율과 94％ 이상의 산화프로필렌(propylene oxide, PO) 선택도를 얻을 수 있었다. 한편 아세토나이트릴(acetonitrile) 용매 하에서 반응 실험을 한 결과 Ti-MCM-22는 99％의 $H_2O_2$ 전화율과 100％에 근접하는 산화프로필렌 선택도를 보이며, 양론비에 가까운 수율을 보였다.

• Elastomers and Composites
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• 제4권1호
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• pp.22-33
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• 1969

• 공업화학
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• 제8권5호
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• pp.866-871
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• 1997

전분의 친수성 및 반응성을 조절하기 위하여 propylene oxide, 1,2-epoxybutane, glycidyl methacrylate, maleic anhydride, caprolactone 등을 반응시켰으며 건조되지 않은 전분을 사용할 경우 propylene oxide, maleic anhydride 외에는 반응 수율이 아주 낮아지는 것이 관찰되었다. 이렇게 개질된 전분을 스티렌과 반응시켜 그라프트 공중합물로 전환하였으며 여러가지 중합방법에 대한 그라프트 수율이 비교되었다. 그라프트 중합반응의 경우 용액중합 및 cerium(IV)이온에 의한 중합은 각각 낮은 효율과 수율을 보였다. 현탁중합 방법으로는 전분 입자의 친수성 때문에 폴리스티렌으로 전분을 encapsulation 하기가 어려웠으며, 유화중합이 스티렌을 그라프트 시키기에 제일 적당한 방법임을 알 수 있었다.

• 한국산학기술학회논문지
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• 제5권6호
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• pp.521-525
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• 2004

Poly(ethylene carbonate)(PEC)와 유사한 카보네이트 삼원공중합체의 생분해성이 시험관(in vitro)에서 연구 되었다. PEC는 온실가스 가운데 하나인 이산화 탄소와 ethylene oxide(EO)를 zinc glutarate 촉매로 이용하여 합성되었고, 삼원공중합체는 EO, cyclohexene oxide(CHO)와 이산화 탄소로 만들었다. PEC와 EO를 포함하는 삼원공중합체는 생분해성을 보였으나 poly(propylene carbonate)(PPC)와 poly(cyclohexene carbonate)(PCHC)는 거의 분해되지 않았다. 생분해성은 무게 감소, FT-IR, SEM 등으로 확인하였다.

• Journal of the Korean Wood Science and Technology
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• 제10권4호
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• pp.38-52
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• 1982

The effect of propylene oxide, butylene oxide, furan resin, and vinylpyrrolidinone in controlling wood dimensional stability have been examined. Wood in the green or ovendry condition was treated with various chemical treatments using a vacuum-pressure procedure, and treated specimens were tested for tangential sweelling, moisture gain, and changes in sorption hysteresis. Results' indicate that propylene oxide, and butylene oxide enhanced with the crosslin king agent trimethylol propane trimethacrylate and applied to ovendry wood were the most efficient chemical treatments in controlling tangential sweeling caused by liquid water or water vapor, and in reducing water vapor adsorption. The sorption behavior of treated wood as depicted by the ratios of sorption was "very favorable" in most instances. In the particular case of furan resin treatments, ratios of sorption were improved from 25 to 100 percent as compared to those of untreated wood.

• Bulletin of the Korean Chemical Society
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• 제23권4호
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• pp.633-636
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• 2002

• Bulletin of the Korean Chemical Society
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• 제28권11호
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• pp.2025-2028
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• 2007

Homogeneous zinc tetrahalide complexes, highly active catalysts for the coupling reactions of alkylene oxide and CO2 produce alkylene carbonates, were heterogenized due to their tendency to decompose produced alkylene carbonates during the distillation process. Heterogenization of homogeneous zinc tetrahalide complexes was achieved by polymerizing 1-alkyl-3-vinylimidazolium zinc tetrahalides. These polymerized zinc tetrahalide catalysts displayed similar activities to their corresponding monomeric analogues for the coupling reactions of carbon dioxide with ethylene oxide (EO) or propylene oxide (PO) to produce ethylene carbonate (EC) or propylene carbonate (PC). TGA studies showed that the polymer-supported zinc tetrahalide catalysts are thermally stable up to 320 oC. The catalyst recycle test showed that the supported catalysts could be reused over six times. After removal of the polymer-supported catalyst through a simple filtration, EC was able to be isolated without decomposition.

• 한국대기환경학회지
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• 제27권4호
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• pp.387-394
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• 2011

A study on the removal of sulfur dioxide and nitrogen oxide was carried out using a non-thermal nano-pulse corona discharger at different gas temperatures. Pulse voltage with a high voltage of 50 kV, a pulse rising time of about 100 ns, a full width at half maximum of about 500 ns and a frequency of 1 kHz was applied to a wire-cylinder corona reactor. Ammonia and propylene gases were added into the corona reactor as additives with a static mixer. Ammonia addition had less effect on $SO_2$ reduction at the higher temperature because of the retardation of ammonium sulfate formation. However, propylene addition enhanced NO reduction at higher temperature due to increased gas mixture. $SO_2$ was further removed at the mixed $SO_2$ and NO gas due to increased $NO_2$ by the conversion of NO. The addition of ammonia and propylene gases was more highly dominant for the removal of sulfur dioxide compared to the sole pulse corona without the additives. However, the specific energy density per unit concentration of pulse corona as well as propylene additive was an important factor to remove NO gas. Therefore, the specific energy density per unit concentration of 0.04 Wh/($m^3{\cdot}ppm$) was necessary for the NO removal of more than 80% with the concentration ratio of 2.0 for propylene and NO. Hydrogen peroxide was another alternative additive to remove both $SO_2$ and NO in the nano-pulse corona discharger.