• 제목/요약/키워드: Tetrahydrofuran(THF)

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역상 액체크로마토그래피에 있어서 이성분과 삼성분 이동상에 대한 페놀류의 머무름 거동 (Retention Behavior of the Phenols on the Binary and Ternary Mobile Phases in Reversed-Phase Liquid Chromatography)

  • 오대섭;이선행;김수한;김상태
    • 대한화학회지
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    • 제30권4호
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    • pp.352-358
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    • 1986
  • 페놀류의 머무름 거동에 대한 실험적 관찰을 이성분용매인 MeOH-Water, ACN-Water, THF-Water와 삼성분용매인 MeOH-Water, ACN-Water, THF-Water계에서 수행했다. 이 머무름 거동의 데이타들로써 용매의 성분비에 따른 크기인자를 예측할 수 있는 선형방정식을 얻었다. 또 페놀류의 최적 분리에 적합한 MeOH-Water이성분 용매를 기준하여 이론적으로 용매세기가 같은 이성분과 삼성분용매를 사용했고 이 등용매세기하에서 시료에 대한 머무름 거동의 특이성 효과는 이성분용매계가 삼성분용매계보다 더 크게 나타났다.

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Tetrahydrofuran-Containing Crown Ethers as Ionophores for NH+4-Selective Electrodes

  • Jin, Hua-Yan;Kim, Tae-Ho;Kim, Jin-Eun;Lee, Shim-Sung;Kim, Jae-Sang
    • Bulletin of the Korean Chemical Society
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    • 제25권1호
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    • pp.59-62
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    • 2004
  • The ammonium ion-selective electrodes ($NH^+_4$-ISEs) based on the tetrahydrofuran(THF)-containing-16-crown-4 derivatives,1,4,6,9,11,14,16,19-tetraoxocycloeicosane ($L^1$) and 5,10,15,20,-tetramethyl-1,4,6,9,11,14,16,19-tetraoxocycloeicosane ($L^2$), were prepared and the electrode characteristics were tested. The conditioned $NH_4^+$-ISEs (E1) based on $L^1$ with TEHP as a plasticising solvent mediator gave best results with near-Nernstian slope of 53.9 mV/decade of activity, detection limit of $10^{-4.9}$ M, and enhanced selectivity coefficients for the $NH^+_4$ ion with respect to an interfering $K^+$ ion (log $K^{pot}_{NH_4^+,K^+}$ = -1.84). This result was compared to other ammonium ionophores reported previously, for example, that of nonactin (log $K^{pot}_{NH_4^+,K^+}$ = -0.92). The proposed electrode showed no significant potential changes in the range of 3.0 < pH < 9.0.

Solution Mixing법에 의한 PS/MWCNT 복합재료의 열 및 전기전도 특성: MWCNT 표면 개질의 영향 (Thermal and Electrical Properties of PS/MWCNT Composite Prepared by Solution Mixing: Effect of Surface Modification of MWCNT)

  • 박은주;이정우;정동수;심상은
    • Elastomers and Composites
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    • 제45권1호
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    • pp.17-24
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    • 2010
  • 본 논문에서는 MWCNT/PS 복합재료 제조 시, MWCNT의 표면 개질에 의한 분산도에 따른 열 및 전기전도도에 관하여 연구하였다. 다양한 종류의 MWCNT를 PS/THF 용액에서 분산시킨 후 침전을 통하여 복합재료를 제조하였다. 사용된 MWCNT는 pristine MWCNT의 상이동 촉매 존재 하에서 상온에서 $KMnO_4$를 이용하여 하이드록실기로 개질된 MWCNT, BYK-9077 분산제를 이용한 MWCNT를 사용하였다. 분석 결과 MWCNT의 PS/THF 용액 내에서의 분산 안정성은 최종 제조되어진 복합재료의 열 및 전기전도도 특성 향상에 중요하게 기여하였다. PS/3 wt% pristine MWCNT에 비하여, 특히 분산제 BYK-9077을 사용한 경우에는 열전도도가 9.7% 및 전기전도도가 30~50% 향상되는 결과를 얻었다.

중성운반체를 이용한 리튬이온 선택 전극 (Lithium Ion Selective Electrode Based on a Synthetic Neutural Carrier)

  • 김재상
    • 분석과학
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    • 제5권1호
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    • pp.33-39
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    • 1992
  • 리튬이온의 새로운 중성운반체로서 tetrahydrofuran 단위의 16고리형 crown-4를 퓨란과 아세톤으로부터 산 촉매하에서 합성하여 수소화시킨 후 리튬-이온과의 착물형성반응을 Li-7 NMR과 전기전도도법으로 조사했다. 합성한 리간드를 PVC-액체막 전극에 사용하여 분리용액법에 의한 리튬이온의 선택성을 결정하였다. 막용매, tris(2-ethylhexyl) phosphate에서 리튬이온의 선택계수는 알칼리금속이온 및 알칼리토금속이온에 대해 $2.4{\times}10^{-1}$에서 $2.3{\times}10^{-4}$ 범위의 값을 가졌으며, 산성용액(pH=2 이하, 0.1M LiCl)에서 액체막은 $H^+$ 이온의 방해로 불안정하였다.

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수소화붕소리튬, 보란 및 보란-염화리튬 (1 : 0.1)에 의한 카르보닐화합물의 선택환원 (Selective Reduction of Carbonyl Compounds with Lithium Borohydride, Borane, and Borane-Lithium Chloride (1 : 0.1) in Tetrahydrofuran)

  • 윤능민;차진순
    • 대한화학회지
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    • 제22권4호
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    • pp.259-267
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    • 1978
  • 수소화붕소리튬, 보란 그리고 보란-염화리튬(1:0.1)의 카르보닐화합물 환원에 있어서의 선택성을 5쌍의 대표적인 카르보닐화합물 쌍(벤즈알데히드-아세토페논, 벤즈알데히드-2-헵탄온, 2-헵탄온-벤조페논, 아세토페논-벤조페논, 2-헵탄온-아세토페논)에 대해서 이들 수소화물의 제한된 양을 반응시켜 알아보았다. 이들 수소화물중 보란-염화리튬(1:0.1)이 제일 선택성이 좋았고, 수소화붕소 리튬과 보란도 2-헵탄온-아세토페논 쌍을 제외하고는 좋은 선택성을 보였다.

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가스 하이드레이트 형성 원리를 이용한 연소전 탈탄소화 연구 (Pre-Combustion Capture of Carbon Dioxide Using Principles of Gas Hydrate Formation)

  • 이현주;이주동;김양도
    • 한국재료학회지
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    • 제18권12호
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    • pp.650-654
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    • 2008
  • The emission of carbon dioxide from the burning of fossil fuels has been identified as a major contributor to green house emissions and subsequent global warming and climate changes. For these reasons, it is necessary to separate and recover $CO_2$ gas. A new process based on gas hydrate crystallization is proposed for the $CO_2$ separation/recovery of the gas mixture. In this study, gas hydrate from $CO_2/H_2$ gas mixtures was formed in a semi-batch stirred vessel at a constant pressure and temperature. This mixture is of interest to $CO_2$ separation and recovery in Integrated Coal Gasification (IGCC) plants. The impact of tetrahydrofuran (THF) on hydrate formation from the $CO_2/H_2$ was observed. The addition of THF not only reduced the equilibrium formation conditions significantly but also helped ease the formation of hydrates. This study illustrates the concept and provides the basic operations of the separation/recovery of $CO_2$ (pre-combustion capture) from a fuel gas ($CO_2/H_2$) mixture.

EPDM 고무에 Acrylonitrile과 4-Chlorostyrene의 그라프트 공중합 (Graft Copolymerization of Acrylonitrile and 4-Chlorostyrene onto EPDM Rubber.)

  • 박덕제;하창식;이진국;조원제
    • Elastomers and Composites
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    • 제24권2호
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    • pp.110-121
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    • 1989
  • The radical initiated graft copolymerization of acrylonitrile(AN) and 4-chlorostyrene(4-Clst) onto ethylene-propylene-diene terpolymer(EPDM) rubber was investigated under various conditions. Graft copolymer(AU-EPDM-4-Clst) was isolated b: selective solvent extraction and identified by using IR spectroscopy. The percent grafting is determined as a function of solvent, reaction time, and monomer mole ratio. Percent grafting decreased in the order of tetrahydrofuran(THF)>THF/ethyl acetate(EA)(1 : 1)>cyclohexane/EA(1 : 1)>n-hexane/EA(1 : 1). Grafting increased continuously with increasing the reaction time up to 40 hr, beyond which the grafting levelled off. It was observed that percent grafting increased as increasing [4-Clst]/[AN] mole ratio, but decreased when [4-Clst]/[AN] mole ratio was higher than 1.60. The light resistance of graft copolymer(AN-EPDM-4-Clst) was better than that of ABS.

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The Observation of Nucleation & Growth during Water Vapor Induced Phase Inversion of Chlorinated Poly(vinyl chloride) Solution using SALS

  • Jang, Jae Young;Lee, Young Moo;Kang, Jong Seok
    • Korean Membrane Journal
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    • 제6권1호
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    • pp.61-69
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    • 2004
  • Small angle light scattering (SALS) and field emission scanning electron microscope (FE-SEM) have been used to investigate the effects of alcohol on phase separation of chlorinated poly(vinyl chloride) (CPVC)/tetrahydrofuran (THF)/alcohol (9/61/30 wt%) solution during water vapor induced phase separation. A typical scattering pattern of nucleation & growth (NG) was observed for all casting solutions of CPVC/THF/alcohol. In the case of the phase separation of CPVC dope solution containing 30 wt% ethanol or n-propanol, the demixing with NG was observed to be heterogeneous. Meanwhile, the phase separation of CPVC dope solution with 30 wt% n-butanol was found to be predominantly homogeneous NG. Although the different phase separation behavior of NG was observed with types of alcohol additives, the resultant surface morphology had no remarkable differences. That is, even though the NG process by water vapor is either homogeneous or heterogeneous, this difference does not play a main role on the final surface morphology. However, it was estimated from the result of hydraulic flux that the phase separation by homogeneous NG provided the membrane geometry with lower resistance in comparison with that by heterogeneous one.

Solvent-Induced Photoemissions of High-Energy Chromophores of Conjugated Polymer MEH-PPV: Role of Conformational Disorder

  • Traiphol, Rakchart;Charoenthai, Nipaphat
    • Macromolecular Research
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    • 제16권3호
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    • pp.224-230
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    • 2008
  • This study examined the photoemission behaviors of isolated chains of poly[2-methoxy, 5-(2'-ethylhexyloxy)-1,4-phenylenevinylene](MEH-PPV) dispersed in various solvents including dichloromethane, chloroform and tetrahydrofuran(THF). A change in polymer-solvent interactions in these solutions caused the MEH-PPV chains to adopt different local conformations, which in turn affected their radiative de-excitation pathways. For the polymer in dichloromethane and chloroform, in which the conjugated chains are relatively extended, photoemission occurs mostly at the long chromophores with lowest HOMO-LUMO energy gap. Their emission spectra showed a main peak at ${\sim}560\;nm$. Dual photoemission of high- and low-energy chromophores was observed when the conjugated chains were forced to partially collapse in a poor solvent THF. Novel high-energy peaks and a typical low-energy peak were detected at ${\sim}414\;nm$ and ${\sim}554\;nm$, respectively. The observation of the high-energy peaks indicates significant suppression of the intrachain energy transfer process, which was attributed to the increase in conformational disorder in the partially collapsed coils. An analysis of the excitation spectra suggests that the high-energy peaks belong to short chromophores constituting of one or two repeat units. This study systematically investigated the effects of polymer concentration, temperature and single bond defects along the backbone on the photoemission of the high-energy chromophores.

이중벽 탄소나노튜브의 염산처리 시간에 따른 전계방출 특성 평가 (Field Emission Characteristics of Double-walled Carbon Nanotubes Related with Hydrochloric Acid Treatment)

  • 정다미;석중현
    • 한국진공학회지
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    • 제20권1호
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    • pp.70-76
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    • 2011
  • 전자 방출원 및 디스플레이 응용분야에서 우수한 가능성을 보이고 있는 이중벽 탄소나노튜브를 Tetrahydrofuran (THF) 열분해 방법으로 대량 합성하였다. 합성된 이중벽 탄소나노튜브는 불순물로 비정질 탄소와 금속촉매를 포함하고 있어, 이를 제거하기 위해 열처리와 과산화수소, 질산, 염산을 이용한 산 처리를 하였다. 정제된 이중벽 탄소나노튜브를 계면 활성제인 Sodium dodecylbenzenesulfonate (SDBS)를 사용하여 잉크를 제작하였고, 잉크를 스프레이 방법으로 Indium Tin Oxide (ITO)기판에 분무하여 전계방출을 위한 에미터를 제작하였다. 본 연구에서는 염산 처리 시간에 따른 이중벽 탄소나노튜브의 특성을 X-ray diffraction, Thermal Gravity Analysis (TGA) 측정을 통해 평가하였고, 염산 처리 시간이 증가할수록 전계방출 특성이 향상되는 것을 FE-current 측정으로 확인하였다.