• 전기화학회지
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• 제13권3호
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• pp.181-185
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• 2010

전도성 고분자로 널리 알려진 폴리아닐린과 액체전해질의 핵심 재료인 이온성 액체와의 복합체를 형성시키고 이들의 물리적, 전기화학적인 특성을 조사되었다. 이미다졸늄 이온성 액체 (1-methyl-3-propylimidazolium iodide, PMI-I)에 비전도성 폴리아닐린 (Emeraldine Base)을 30 wt%이상 첨가하였을 때 준고형화 현상이 나타났고, 이온성 액체의 이미다졸늄 양이온의 방향족 고리와 폴리아닐린의 벤족기와의 ${\pi}-{\pi}$ 자기상호조립에 의한 약한 도핑작용을 통해 섬유상 구조를 나타내었으며, 전도도의 변화율은 80%이상 유지하였다.

• Journal of Electrochemical Science and Technology
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• 제8권3호
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• pp.257-264
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• 2017

A polymeric ionic liquid, poly(1-methyl 3-(2-acryloyloxypropyl) imidazolium iodide) (PMAPII), was synthesized as a single-iodide-ion-conducting polymer and employed in a gel polymer electrolyte. Gel polymer electrolytes prepared from iodine, 4-tert-butylpyridine, ${\gamma}$-butyrolactone, and PMAPII were applied in quasi-solid-state dye-sensitized solar cells (DSSCs). The addition of 16 wt.% PMAPII provided the most favorable environment, striking a compromise between the iodide ion concentration and the ionic mobility, which resulted in the highest conversion efficiency of the resulting DSSCs. The quasi-solid-state DSSC assembled with the optimized gel polymer electrolyte exhibited a relatively high conversion efficiency of 7.67% under AM 1.5 illumination at $100mA\;cm^{-2}$ and better stability than that of the DSSC with a liquid electrolyte.

• Bulletin of the Korean Chemical Society
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• 제34권1호
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• pp.225-230
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• 2013

A new heteropolyanion-based ionic ($[Hmim]_5PMo_{10}V_2O_{40}$) was synthesized by the reaction of molybdovanadophosphoric acid ($H_5PMo_{10}O_{40}$) with N-methylimidazole. [$[Hmim]_5PMo_{10}V_2O_{40}$ showed a high catalytic activity in the oxidative desulfurization of sulfur-containing compounds in 1-methylimidazolium tetrafluoroborate ($[Hmim]BF_4$) ionic liquid using 30% aqueous $H_2O_2$ as the oxidant. The catalytic system was of high activity, simplified workup and flexible recyclability. The catalytic oxidation reactivity of sulfur-containing compounds decreased in the order dibenzothiophene (DBT) > 4,6-dimethyldibenzothiophene (4,6-DMDBT) > benzothiophene (BT). The influences of various parameters including reaction time (t) and temperature (T), catalyst dosage, and oxidant to sulfur molar ratio n(O)/n(S) on the desulfurization of model oil were investigated in details. 99.1% of DBT conversion in the model oil was achieved at atmospheric pressure under the optimal conditions: n(O)/n(S) = 4:1, $60^{\circ}C$, 100 min and molar ratio of catalyst to sulfur of 0.062. The ionic liquid can be recycled six times without significant decrease in activity.

• 전기화학회지
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• 제12권3호
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• pp.271-275
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• 2009

Five novel lithium polyelectrolyte-ionic liquid systems, using poly (lithium 2-acrylamido-2-methyl propanesulfonate; PAMPSLi) were prepared and their electrochemical properties were measured. The ionic conductivity of the PAMPSLi/1-ethyl-3-methylimidazolium tricyano methanide (emImTCM) system was exhibited high conductivity (1.28 $\times$ $10^{-3}$ $S/cm^{-1}$). The high conductivity and low viscosity of PAMPSLi/emImTCM system is due to the high flexibility of imidazolium cation and dissociation of lithium cation from the polymer chains. The PAMPSLi/N,N-dimethyl-N-propyl-Nbutylammonium tricyanomethanide ($N_{1134}TCM$) and PAMPSLi/N, N-dimethyl-N-propyl-N-butylammonium dicyanamide ($N_{1134}DCA$) systems showed fairly high conductivity (6.3 $\times$ $10^{-4}$ $S/cm^{-1}$, 6.0 $\times$ 10.4 S/cm.1). PAMPSLi/Trihexyl (tetradecyl) phosphonium bis (trifluoromethane sulfonyl) amide ($P_{66614}TFSA$) exhibited low conductivity (2.22 $\times$ $10^{-5}$ $Scm^{-1}$) and thermally stable over 400$^{\circ}C$.

• Bulletin of the Korean Chemical Society
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• 제30권5호
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• pp.1009-1011
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• 2009

Nano-structured conducting polypyrroles were synthesized in the ionic liquids (ILs) based on 1-alkyl-3-methylimidazolium family with tetrachloroferrate as an anion ($C_n\;mim\;[FeCl_4]\;with\;n\;=\;4,\;8,\;and\;12$). The polypyrrole nanostructures synthesized in ILs were formed as spherical shapes. For ionic liquids with alkyl side chain length $C_4,\;C_4\;mim\;[FeCl_4]$, the size of particles was ranged around 60-nm with a relatively narrow size distribution. As the length of alkyl chain increases, the particle sizes become larger and their distributions become wider. The self-assembled local structures in the solvent ionic liquids are likely to serve as templates of highly organized nano-structured polymers. The length of the alkyl chain in ionic liquids seems to affect these local structures.

• 한국에너지공학회:학술대회논문집
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• 한국에너지공학회 2010년도 춘계학술 발표회
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• pp.199-199
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• 2010

Polymeric membranes have been widely used to separate gas mixtures, such as $O_2/N_2,\;CO_2/CH_4,\;CO_2/N_2$, and olefin/paraffin. The permeation selectivity is the ratio between composition ratio at the permeate side and composition ratio at the feed side. In addition, the permeation selectivity is a product of solubility selectivity and diffusivity selectivity. We present a novel idea and describe its experimental result, which was achieved by preparing polymer gel films that included a room temperature ionic liquid (RTIL) in a polymer matrix. It is known that $CO_2$ can dissolve easily in imidazolium-based RTILs. We prepared polymer-ionic liquid gel films using an ionic liquid, 1-ethyl-3-methylimidazolium acetate ([emim] acetate, C-tri) and a host polymer, poly (vinyl acetate) (PVAc, Aldrich).

• Bulletin of the Korean Chemical Society
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• 제26권4호
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• pp.599-602
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• 2005

The aromatic fluorination method involving the acid-catalyzed decomposition of a triazene in an ionic liquid is a very convenient and efficient way to prepare a variety of aromatic fluorides in a lab-scale. It should be particularly useful for the preparation aryl fluorides substituted with electron withdrawing substituents. Fluorination of triazene 1 (1.0 mmol) and p-toluenesulfonic acid (1.2 mmol) in an ionic liquid, 1-butyl-3-methylimidazolium tetrafluoroborate ([bmim][$BF_4$], 2.5 mL) proceeds very smoothly at 80 ${^{\circ}C}$ with or without an external source of fluoride, providing 73% yield in 30 min. Unlike diazonium salts, triazene precursors are stable enough to be stored for a long period of time without a noticeable decomposition.

• 청정기술
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• 제12권3호
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• pp.128-137
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• 2006

초임계이산화탄소 내에서 이온성액체의 부피 변화와 상온 이온성액체와 유기화합물의 혼합물이 두 상으로 분리되는 현상을 고압 view cell을 이용하여 측정하였다. 이온성액체(ionic liquid, IL)로는 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim][$PF_6$])와 1-butyl-3-methylimidazolium tetrafluoroborate ([bmim][$BF_4$])를 사용하였으며, 유기화합물로는 methanol과 dimethyl carbonate를 사용하였다. 일정한 양의 [bmim][$PF_6$]에 대하여 유기화합물의 양을 증가시킴에 따라 상이 나누어지는 지점인 lower critical end point (LCEP) 압력이 감소하였다. 이온성액체의 수분함량이 증가함에 따라 LCEP가 높게 나타났으며, 일정량 이상의 수분이 함유되어 있으면 LCEP가 나타나지 않았다. LCEP는 같은 부피의 [bmim][$PF_6$]에서보다 [bmim][$BF_4$]에서 약 1.0 MPa 정도 높게 나타났으며, K-point는 이온성액체의 종류와 유기화합물의 양에 따라 거의 변화하지 않았다. 초기시료 중 이온성액체([bmim][$PF_6$])의 농도 (IL/(IL+MeOH))가 7.23 mol% 보다 크면 혼합물의 LECP에서 $L_1$의 부피가 $L_2$의 부피보다 크게 나타났으며, 반대로 작으면 작게 나타났다. 이산화탄소의 존재 하에서 이온성액체의 부피변화는 온도가 증가함에 따라 감소하였으며, 313.15 와 343.15 K 사이에서는 압력이 증가함에 따라 증가하여 300 bar에서는 원래 부피의 123~126 %가 되었다.

• Korean Chemical Engineering Research
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• 제44권5호
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• pp.453-459
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• 2006

두 개의 D-아미노산 물질을 분리함에 있어서 이온성 액체의 영향을 고찰하였다. 아미노산 물질로서 D-tryptophan과 N-CBZ-D-phenylalanine을 사용하였으며, 이온성 액체로서 1-butyl-3-methylimidazolium tetrafluoroborate(${[BMIm]}^+{[BF_4]}^-$)을 사용하였고, 역상 액체 크로마토그래피로 분석하였다. 이동상은 각각 65％, 70％, 80％ 메탄올을 주성분으로 0.5, 1.0, 1.5, 2.0, 4.0, 6.0, 8.0, 10.0, 12.0과 15.0 mmol/L의 농도의 이온성 액체를 첨가하였고, 칼럼($3.9{\times}300mm$)에 $15{\mu}m$의 입자 크기를 가진 $C_{18}$ 실리카 겔을 충진하여 사용하였다. 이온성 액체를 첨가함으로써 D-tryptophan의 체류인자는 거의 변화가 없었지만, N-CBZ- D-phenylalanine의 체류인자는 감소하였다. 두 물질의 분리도는 메탄올의 함량과 이온성 액체의 농도에 따라 변화하였다. 메탄올의 함량이 낮을수록, 이온성 액체의 농도의 증가에 따라서 분리도는 증가하는 경향을 나타내었다

• 융복합기술연구소 논문집
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• 제4권1호
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• pp.5-8
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• 2014

Recently ionic liquids received much attention as novel materials capable of replacing traditional solvents. The applicability of the ionic liquids should be determined based on their physico-chemical properties. Heat capacity is one of the most important properties to be considered when a process is developed using the ionic liquids and currently DSC has been proved as an effective technique to measure the heat capacity. Micro DSCII can measure heat capacities of various liquids by both an isothermal step method and a scanning method. DSC Q100 and MDSC are able to measure heat capacities of several ionic liquids. For each ionic liquid linear regression of the heat capacity as a function of temperature has been performed to increase accuracy. To investigate the feasibility of ionic liquids as PCMs, their heat capacities have been measured by using Pysis I DSC. This paper briefly summarizes the present techniques of measuring heat capacities of ionic liquids by DSC.