• Title/Summary/Keyword: 카보네이트합성

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Synthesis of Cyclic Carbonates under Supercritical Condition (초임계상에서 고리형 카보네이트의 합성)

  • Yoo, Jin-Yi;Jun, Joon-Ho;Sung, Un-Gyung;Lee, Yoon-Bae
    • Proceedings of the KAIS Fall Conference
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    • 2007.05a
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    • pp.264-266
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    • 2007
  • 지구의 온난화를 가속시키는데 일조하고 있는 이산화탄소($CO_{2}$)와 Epoxy를 Tetrabutylammonium bromide를 촉매로 하여 초임계 상태에서 반응시켜 2차 전지의 전해질 물질로 사용 가능한 4-ethyl-l,3-dioxolan-2-one, 4-methyl-1,3-dioxlan-2-one, 4-phenyl-1,3-dioxolan-2-one, 4-Chloromethyl-1,3-dioxolan-2-one을 합성하여 $^{l}H-NMR$을 이용하여 분석하였다.

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Synthesis of Biodegradable Polymers with Carbon Dioixde (이산화탄소를 이용한 생분해성 고분자의 합성)

  • Shin Sang Chul;Shin Jae Shik;Lee Yoon Rae
    • Journal of the Korea Academia-Industrial cooperation Society
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    • v.5 no.6
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    • pp.521-525
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    • 2004
  • Biodegradation of poly(ethylene carbonate) (PEC) and their terpolymers has been investigated in vitro. PEC has been synthesized with ethylene oxide (EO) and carbon dioxide, which is one of the greenhouse gases using Zinc glutarate has been used as catalyst Carbonate terpolymers have been prepared by the use of EO, cyclohexene oxide(CHO), and carbon dioxide. High biodegradability of PEC and terpolymers with EO. has been observed. Very low biodegradation of poly(propylene carbonate) (PPC) and poly(cyclohexene carbonate) (PCHC) has been shown. The weight loss, FT-IR and SEM have been employed to characterize biodegradability.

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Synthesis of Cyclic Carbonates under Supercritical Carbon Dioxide (초임계 $CO_2$ 상에서의 고리형 카보네이트의 합성)

  • Yoo, Jin-Yi;Jun, Joon-Ho;Sung, Un-Gyung;Lee, Yoon-Bae
    • Proceedings of the KAIS Fall Conference
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    • 2007.11a
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    • pp.347-349
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    • 2007
  • 지구 온난화를 일으키는 온실 가스 중의 하나인 이산화탄소($CO_2$)를 Epoxide와 Tetrabutylammonium bromide를 촉매로 하여 합성하여, 초임계 $CO_2$ 상태($Tc=31.06^{\circ}C$, Pc=7.38MPa)에서 반응하여 그에 따른 수율을 측정한 결과 초임계하에서는 현저한 수율의 증가를 확인하였다.

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Study on GO Dispersion of PC/GO Composites according to In-situ Polymerization Method (In-situ 중합방법에 따른 폴리카보네이트(PC)/그래핀 옥사이드(GO) 복합체의 GO 분산성 연구)

  • Lee, Bom Yi;Park, Ju Young;Kim, Youn Cheol
    • Applied Chemistry for Engineering
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    • v.26 no.3
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    • pp.336-340
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    • 2015
  • Three different types of polycarbonate (PC)/graphene oxide (GO) composites using diphenyl carbonate as a monomer were fabricated by melt polymerization. Those were the PC/GO composite (PC/GO) using a twin extruder, in-situ PC/GO composite (PC/GO-cat.) using a catalyst, and in-situ PC/GO composite (PC/GO-COCl) using a GO-COCl treated by -COCl, Chemical structures of the composites were confirmed by C-H and C=O stretching peak at $3000cm^{-1}$ and $1750cm^{-1}$, respectively. The slope for the storage (G') versus loss (G") modulus plot decreased with an increase in the heterogeneous property of polymer melts. So we can check the GO dispersion of the PC/GO composites using by the slop for G'-G" plot. According to the G'- G" slopes for three different types of PC/GO composites, GO was well dispersed within PC matrix in case of PC/GO and PC/GO-cat.. It was also confirmed by atomic force microscope (AFM) photos. One of the reasons for the poor GO dispersion of PC/GO-COCl is branching and crosslinking processes occurred during polymerization, which was further confirmed by a plot for the complex modulus versus phase difference.

Characteristics of Dental Restorative Composite Resins Prepared from 2,2-bis- [4- (2-hydroxy-3-rnethacryloyloxy propoxy) phenyl] propane Derivatives and Spiro Orthocarbonate (2,2-비스[4-(2-하이드록시-3-메타크릴로일옥시프로폭시)페닐] 프로판 유도체와 스파이로 오쏘카보네이트가 포함된 치아 수복재의 특성)

  • Kim Yong;Lee Juyeon;Park Kwangyong;Kim Chang Keun;Kim Ohyoung
    • Polymer(Korea)
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    • v.28 no.5
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    • pp.426-432
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    • 2004
  • To reduce volumetric shrinkage of the commercially available polymeric dental composite during curing reaction, (2,2-bis [4-(2-hydroxy-3-methacryloyloxy propoxy) phenyl] propane) (bis -GMA) derivatives, i.e., (2,2-bis[3-methyl, 4-(2-hydroxy-3-methacryloyloxy propoxy) phenyl] propan) (DMBis-GMA) and (2,2-his [3,5-dimethyl ,4- (2-hydroxy-3-methacryloyloxy propoxy) phenyl] propane) (TMBis-GMA) were synthesized and then new dental composite resin composed of Bis-GMA derivatives, diluent, spiro orthocarbonate (SOC), and inorganic filler was produced. Among the Bis-GMA derivative/Bis-GMA derivative/diluent mixtures, Bis-GMA/ TMBis-GMA/TEGDMA mixture exhibited the lowest volumetric shrinkage. Volumetric shrinkage of this mixture was further reduced by adding SOC. Volumtric shrinkage of dental composite prepared from commercially available resin monomer mixture was $2.5\%$, while that prepared from resin monomer mixture having minimum volumetric shrinkage was reduced to $0.7\%$. Mechanical strength of this dental composite was nearly the same with that of commercial products but the time required for the curing reaction was retarded.

Effect of Strontium Carbonate Inorganic Binder Addition on Ceramic Candle Filter Matrix (세라믹 캔들 필터 지지체의 스트론튬 카보네이트 무기결합재 첨가 영향)

  • Han, Insub;Seo, Doowon;Hong, Kiseog;Kim, Seyoung;Yu, Jihang;Woo, Sangkuk
    • 한국신재생에너지학회:학술대회논문집
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    • 2010.06a
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    • pp.109.2-109.2
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    • 2010
  • 세라믹 필터는 여러 종류의 분진제거 시스템에서 연소 배가스 정제를 위한 가장 적절한 소재로 알려져 있다. 현재까지 다양한 형태의 세라믹 필터가 개발되고 있는데, 캔들 타입(candle type), 튜브 타입(tubular type), 평판 타입(parallel flow type) 등이 그 예이다. 통상적으로 세라믹 캔들 필터는 가압유동층복합발전(PFBC, Pressurize Fluidized-Bed Combustion), 석탄가스화복합발전(IGCC, Integrated coal Gasification Combined Cycle), 석탄가스화연료전지복합발전(IGFC, Integrated coal Gasification Fuel cell Combined cycle)에서 고온 배가스 정제용으로 사용되고 있다. 일반적으로 IGCC나 CTL 합성가스 정제시스템의 경우에는 높은 고압(약 25기압)과 미세분진이 함유되어 있는 분위기에서 운전된다. 그러므로 이때 사용되는 초청정용 세라믹 집진필터는 고온, 고압 및 부식 환경에서 50 MPa 이상을 갖는 높은 강도와 내식성을 갖도록 개발되어야 하기 때문에 SiC(Silicon Carbide)가 가장 적절한 캔들 필터 소재로 적용되고 있다. 이에 따라 집진용 SiC 세라믹 캔들 필터를 개발하기 위해서는 고온에서 내산화성이 우수하고, 부피팽창에 의한 균열이 발생하지 않는 무기결합재의 선정 및 이를 통한 소재의 특성 최적화가 가장 중요한 부분이라 할 수 있다. 본 연구에서는 IGCC나 CTL 공정에 적용하기 위한 SiC 캔들 필터 소재 개발을 위해 래밍성형 공정으로 1m급의 탄화규소 캔들 필터 시작품을 제작하여 SiC 출발입자 크기와 무기계 결합재인 스트론튬 카보네이트의 첨가량 변화에 따른 필터 소재의 특성 평가를 수행하였다.

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Catalytic Performance of Ionic Liquids in the Synthesis of Glycerol Carbonate from Glycerol and Urea (글리세롤과 요소로부터 글리세롤카보네이트 합성에서 이온성액체의 촉매 특성)

  • Kim, Dong-Woo;Park, Kyung-Ah;Kim, Min-Ji;Park, Dae-Won
    • Korean Chemical Engineering Research
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    • v.51 no.3
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    • pp.347-351
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    • 2013
  • The preparation of glycerol carbonate (GC) from urea through carbonylation with renewable glycerol was investigated by using ionic liquid catalysts. It was found that quaternary ammonium salt and imidazolium salt ionic liquids with a shorter alkyl chain length and higher nucleophilic anion showed better catalytic performance. The effects of reaction temperature, reaction time and degree of vacuum on the reactivity of TBAC catalyst ware discussed. Zinc chloride ($ZnCl_2$) was used as co-catalyst with the ionic liquid catalyst. The mixed catalyst showed a synergy effect on the glycerol conversion and GC yield probably due to the acid-base properties of the catalysts.

Effect of the Additives on Direct Dimethyl Carbonate Synthesis using Methanol and Carbon Dioxide over Ce0.8Zr0.2O2 Catalyst (Ce0.8Zr0.2O2 촉매 상에서 메탄올과 이산화탄소를 이용한 디메틸카보네이트 직접 합성에 대한 첨가제의 영향)

  • Han, Gi Bo;Park, No-Kuk;Yoon, Suk Hoon;Lee, Tae Jin
    • Korean Chemical Engineering Research
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    • v.45 no.6
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    • pp.554-559
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    • 2007
  • In order to improve the reactivity for the direct synthesis of dimethyl carbonate (DMC) using methanol and carbon dioxide, the various additives were used in the DMC synthesis using $Ce_{0.8}Zr_{0.2}O_2$ catalyst, and then effect of the additives was investigated. The various additives were molecular sieves 3A and the compounds having the various functional groups such as sulfate, carbonate, nitrate and phosphate. As a result, the compound such as $K_2SO_4$ and $Na_2SO_4$ having sulfate group were the most effective additive among the various additives. When $K_2SO_4$ was used as an additive in the direct synthesis of DMC, the amount of DMC was about 0.91 mmol, which was the highest mount of DMC among using only-$Ce_{0.8}Zr_{0.2}O_2$ catalyst and the various additives.

Synthesis of Dimethyl Carbonate from Methanol and Supercritical Carbon Dioxide over K2CO3/ZrO2 Catalysts (메탄올과 초임계 이산화탄소로부터 K2CO3/ZrO2 촉매를 이용한 디메틸카보네이트 (Dimethyl Carbonate) 합성)

  • Hong, Seung Tae;Park, Hyung Sang;Lim, Jong Sung;Yoo, Ki-Pung
    • Korean Chemical Engineering Research
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    • v.46 no.3
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    • pp.550-554
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    • 2008
  • The synthesis of dimethyl carbonate (DMC) from methanol and supercritical carbon dioxide over $K_2CO_3/ZrO_2$ catalysts have been studied. The catalysts were prepared by impregnating $ZrO_2$ with an aqueous $K_2CO_3$ solution. The optimum calcination temperature to disperse K species on the $ZrO_2$ surface was found to be 673 K. Monoclinic $ZrO_2$ was not active, as itself, for the DMC production. However, when the $K_2CO_3$ was impregnated on the $ZrO_2$, the catalytic performance was improved. Besides the catalyst, $CH_3I$ was used as a promoter. The $CH_3I$ promoter as well as the $K_2CO_3/ZrO_2$ catalyst was found to take an important role to improve the production of DMC. The optimum quantities for the catalyst and the promoter were estimated. The effect of the catalyst and the promoter for the DMC synthesis from methanol and supercritical carbon dioxide was investigated and the reaction mechanism was proposed.

Synthesis of the BaTiO$_3$ Powders by the Glyscine-Nitrate Process and Its Properties (Part I) (Glycine-Nitrate 법에 의한 BaTiO$_3$ 분말의 합성 및 그 특성(Part I))

  • 박지애;김구대;이홍림;이동아
    • Journal of the Korean Ceramic Society
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    • v.35 no.8
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    • pp.857-863
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    • 1998
  • The BaTiO3 powders extensively used as MLCC (Multilayer ceramic capacitor) in electronic ceramic in-dustry were synthesized by GNP (Glycine-Nitrate process) The powders were prepared using carbonate and alkoxide as starting materials and nitric acid was used as a solvent for starting materials as well as an oxidant for combustion. The BaTiO3 powders were synthesized using different amounts of glycine as a fuel for combustion. The characteristics of synthesized powders were examined with helium pycnometer X-ray diffraction(XRD) Brunauer-Emmett-Teller with N2 adsorption and scanning electron microscopy(SEM). It was found that single phase BaTiO3 could be formed when the as-synthesized powders were heat-treated at 100$0^{\circ}C$ When the glycine/cation molar ratio was 1,2 specific surface area was 24m2/g

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