• Title/Summary/Keyword: 에틸렌 카보네이트

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Synthesis and Physicochemical Properties of Branched Solid Polymer Electrolytes Containing Ethylene Carbonate Group (에틸렌 카보네이트기를 함유하는 가지형 고체 고분자전해질의 합성 및 물리화학적 특성)

  • Kim, Doo-Hwan;Ryu, Sang-Woog
    • Journal of the Korean Electrochemical Society
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    • v.18 no.4
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    • pp.150-155
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    • 2015
  • In this study polymer electrolytes containing ethylene carbonate group which have a high dielectric constant and poly(ethylene glycol) as branches were prepared by the Williamson reaction between poly(ethylene glycol) methyl ether and block copolymers composed of glycerol-1,2-carbonate and 4-chloromethyl styrene. Interestingly, the highest ionic conductivity of $1.75{\times}10^{-5}S\;cm^{-1}$ was observed from the polymer electrolyte having 7 mol% of ethylene carbonate and the [EO]:[Li] ratio of 32:1. Moreover, it was found that the electrochemical stability of polymer electrolyte was achieved up to 5.5 V because of the presence of ethylene carbonate.

Synthesis of Low Molecular-weight Poly (Propylene Carbonate)-Poly (Ethylene Glycol) Block Copolymers through $CO_2$/Propylene Oxide Copolymerization (이산화탄소/프로필렌 옥사이드 공중합을 통한 저분자량 폴리(프로필렌 카보네이트)-폴리(에틸렌 글리콜) 블록 공중합체의 합성)

  • Lee, Sang-Hwan;Cyriac, Anish;Jeon, Jong-Yeob;Lee, Bun-Yeoul
    • Clean Technology
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    • v.17 no.3
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    • pp.244-249
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    • 2011
  • We synthesized low molecular-weight polymers bearing hydrophobic and hydrophilic parts in a chain through $CO_2$/propylene oxide copolymerization. When hydrophilic poly (ethylene glycol) bearing -OH group (s) at the end group (s) was added as a chain transfer agent in the $CO_2$/propylene oxide copolymerization catalyzed by a highly active catalyst, block polymers were formed. If poly (ethylene glycol) (PEG) bearing -OH group only at an end was fed, PEG-block-PPC diblock copolymer was obtained. When PEG bearing -OH group at both ends was fed, PPC-block-PEG-block-PPC triblock copolymer was obtained. We confirmed formation of block copolymers by $^1H$-NMR spectroscopy and GPC studies.

Synthesis of Bishydroxyethyl Ether of Bisphenol A(BHE-BPA) Through the Depolymerization of Polycarbonate (폴리카보네이트 해중합을 이용한 Bisphenol A계 Bishydroxyethyl Ether 화합물 생성 특성)

  • Heo, Miseon;Kim, Beomsik;Park, Youin;Han, Myungwan
    • Korean Chemical Engineering Research
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    • v.48 no.2
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    • pp.164-171
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    • 2010
  • Recently, the waste of Polycarbonate(PC) is increase with the increase in demand of a polycarbonate. It is concerned with producing a new material and diol monomer, bishydroxyethyl ether of bisphenol A(BHE-BPA) through depolymerization of the polycarbonate waste at recycling. BHE-BPA can be used as a good raw material for the synthesis of polycarbonate type polyurethane. PC particles were depolymerized with base-catalyst NaOH, solvent EG, and ethylene carbonate(EC) was formed during the PC depolymerziation. EC was added to promote the conversion from bispenol-A to BHE-BPA. The characteristics of depolymeraion of polycarbonate as well as conversion of bispenol-A to BHE-BPA were investigated. BHE-BPA yield of 92% was obtained at temperature $220^{\circ}C$, 10% catalyst/PC mole ratio, 20 mmol of EC. BHE-BPA purity of better than 99% was achieved by crystallization of BHE-BPA.

Effect of Vinyl Ethylene Carbonate on Electrochemical Characteristics for Activated Carbon/Li4Ti5O12 Capacitors (활성탄/리튬티탄산화물 커패시터의 전기화학적 특성에 미치는 비닐에틸렌카보네이트의 영향)

  • Kwon, Yong-Kab;Choi, Ho-Suk;Lee, Joong-Kee
    • Journal of the Korean Electrochemical Society
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    • v.15 no.3
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    • pp.190-197
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    • 2012
  • We employed the vinyl ethylene carbonate (VEC) as an electrolyte additive and investigated the effect of the electrolyte additive on the electrochemical performance in hybrid capacitor. The activated carbon was adopted as cathode material, and the $Li_4Ti_5O_{12}$ oxide was used as anode material. The electrolyte was prepared with the $LiPF_6$ salt in the mixed solvent of ethylene carbonate (EC), dimethyl carbonate (DMC), and ethyl methyl carbonate(EMC). We evaluated the electrochemical performance of the hybrid capacitor with increasing the amount of the VEC electrolyte additive, which is known as the remover of oxygen functional group and the stabilizer of the electrode by reducing the surface of electrode, and obtained the superior performance data especially at the addition of the VEC electrolyte additive of around 0.7 vol%. On the contrary, the addition of the VEC more than 0.7 vol% in the electrolyte leads to the degradation in electrochemical performance of hybrid capacitor, suggesting the increase of the side reaction from the excessive VEC additive. X-ray photoelectron spectroscopy (XPS) revealed that the addition of the VEC suppressed the formation of LiF component, which is known as the insulator, on the surface of electrode. The optimized addition of VEC exhibited the improved capacity retention around 82.7% whereas the bare capacitors without VEC additive showed the 43.2% of capacity retention after 2500 cycling test.

A Study on Recycling Technology of EC for Semiconductor and LCD PR Stripping Process (반도체/LCD PR 제거용 EC의 재이용 기술에 관한 연구)

  • Moon, Se-Ho;Chai, Sang-Hoon
    • Journal of the Institute of Electronics Engineers of Korea SD
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    • v.46 no.10
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    • pp.25-30
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    • 2009
  • We have developed recycling technology of ethylen carbonate to use in photoresist stripping and cleaning process, which will be core processing technology for high performance and low price semiconductor and LCD fabrication. Using this technology, it is possible for semiconductor wafer and LCD planer to process more rapid and chip, and productivity will be improved.

Depolymerization of Polycarbonate Waste by Ethylene Glycol (에틸렌글리콜을 이용한 폐폴리카보네이트 해중합 특성)

  • Kim, Dongpil;Kim, Bo-kyung;Cho, Youngmin;Han, Myungwan;Kim, Beom-Sik
    • Korean Chemical Engineering Research
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    • v.46 no.5
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    • pp.875-879
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    • 2008
  • A method for the depolymerization of polycarbonate waste by glycolysis using ethylene glycol without catalyst was explored in order to get the monomer bisphenol A (BPA). The effect of operation variables such as reaction time, reaction temperature, EG/PC weight ratio and the kinetic of glycolysis were studied. It was found that the polymerization reaction has two different activation energies depending on the reaction temperature. A drop in activation energy with temperature indicates that the reaction mechanism has shifted from one of a succession of elementary steps to another in the series. The maximum yield of BPA of 95.6% was achieved at reaction temperature $220^{\circ}C$ for 85min with EG/PC weight ratio 4.

A Kinetic Study on the Synthesis of Dimethylcarbonate by Using Immobilized Ionic Liquid Catalyst (고정화된 이온성 액체 촉매를 이용한 디메틸카보네이트 합성 반응에 대한 속도론적 고찰)

  • Kim, Dong-Woo;Kim, Dong-Kyu;Kim, Cheol-Woong;Koh, Jae-Cheon;Park, DaeWon
    • Korean Chemical Engineering Research
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    • v.48 no.3
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    • pp.332-336
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    • 2010
  • Ionic liquid immobilized on mesoporous amorphous silica was prepared from the coupling of 1-(triethoxysilylpropyl)-3-n-alkyl-imidzolium halides with tetraethyl orthosilicate(TEOS) through template-free condensation under strong acidic conditions. The immobilized 1-n-butyl-3-methyl imidazolium bromide ionic liquid on amorphous silica(BMImBr-AS) was proved to be an effective heterogeneous catalyst for the synthesis of dimethyl carbonate(DMC) from transesterification of ethylene carbonate(EC) with methanol. High temperature, high carbon dioxide pressure and long reaction time were favorable for the reactivity of BMImBr-AS. Kinetic studies based on two step reactions revealed that the proposed reaction model fitted well the experimental data. The apparent activation energy was estimated to be 67.4 kJ/mol.

Depolymerization of Polycarbonate Using Glycolysis/Methanolysis Hybrid Process (폴리카보네이트의 글리콜첨가분해/메탄올첨가분해 복합 해중합)

  • Kim, D.P.;Kim, B.K.;Cho, Y.M.;Kim, B.S.;Han, M.
    • Clean Technology
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    • v.13 no.4
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    • pp.251-256
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    • 2007
  • Several studies regarding depolymerization of polycarbonate waste to get the essential monomer, bisphenol A, have been reported in recent years. However, those methods have some environmental safety problems of using highly toxic organic solvents as well as product separation problem due to the use of alkali catalyst. In this study, we proposed the combination of glycolysis and methanolysis to depolymerize the polycarbonate waste. Glycolysis reaction reached at the reaction equilibrium after about 180 minat 473.15K and dissolution of the polycarbonate was found to be a rate controlling step of the reaction. The yield of BPA was improved with the aid of combination of glycolysis and methanolysis. The methanolysis was carried out at a temperature range of $303.15K{\sim}363.15K$ and MeOH/PC molar ratio $0.5{\sim}3$. The yield of BPA had a maximum at 1.0 MeOH/PC molar ratio and increased with the reaction temperature.

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Effect of ZnCl2 Co-catalyst in the Synthesis of Dimethyl Carbonate from Ethylene Carbonate and Methanol by Using Base Catalysts (염기 촉매를 이용한 디메틸카보네이트 합성에서 ZnCl2 조촉매의 영향)

  • Kim, Dong-Woo;Park, Moon-Seok;Kim, Moon-Il;Park, Dae-Won
    • Korean Chemical Engineering Research
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    • v.50 no.2
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    • pp.217-222
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    • 2012
  • The synthesis of dimethyl carbonate(DMC) is a promising reaction for the use of naturally abundant carbon dioxide. DMC has gained considerable interest owing to its versatile chemical reactivity and unique properties such as high oxygen content, low toxicity, and excellent biodegradability. In this study, the synthesis of DMC through the transesterification of ethylene carbonate(EC) with methanol was investigated by using ionic liquid and metal oxide catalysts. The screening test of different catalysts revealed that choline hydroxide ([Choline][OH]) and 1-n-butyl-3-methyl imidazolium hydroxide([BMIm][OH]) had better catalytic performance than metal salts catalysts such as MgO, ZnO and CaO. The effects of reaction parameters such as reaction temperature, MeOH/EC mole ratio, and carbon dioxide pressure on the reactivity of [Choline][OH] catalyst were discussed. High temperature and high MeOH/EC mole ratio were favorable for high conversion of EC. However, the yield of DMC showed a maximum when carbon dioxide pressure was 1.34 MPa, and then it decreased for higher carbon dioxide pressure. Zinc chloride($ZnCl_2$) was used as co-catalyst with the ionic liquid catalyst. The mixed catalyst showed a synergy effect on the EC conversion and DMC yield probably due to the acid-base properties of the catalysts.