• 한국전기전자재료학회논문지
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• 제22권11호
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• pp.974-979
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• 2009

We studied solution-processed single-layered phosphorescent organic light-emitting diodes (PHOLEDs), doped with ionic salt and treated with simultaneous electrical and thermal annealing. Because the simultaneous annealing causes the accumulation of salt ions at the electrode surfaces, the energy levels of the organic molecules are bent by the electric fields due to the adsorbed ions, i.e., the simultaneous annealing can induce the proper formation of an ionic p-i-n structure. As a result, an ionic p-i-n PHOLED with a peak luminescence of over ${\sim}35,000\;cd/m^2$ and efficiency of 27 cd/A was achieved through increased and balanced carrier-injections.

• Carbon letters
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• 제28권
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• pp.47-54
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• 2018

High surface carbon aerogels with hierarchical and tunable pore structure were prepared using ionic liquid as carbon precursor via a simple salt templating method. The as-prepared carbon aerogels were characterized by nitrogen sorption measurement and scanning electron microscopy. Through instant visual observation experiments, it was found that salt eutectics not only serve as solvents, porogens, and templates, but also play an important role of foaming agents in the preparation of carbon aerogels. When the pyrolyzing temperature rises from 800 to $1000^{\circ}C$, the higher temperature deepens the carbonization reaction further to form a nanoporous interconnected fractal structure and increase the contribution of super-micropores and small mesopores and improve the specific surface area and pore volume, while having few effects on the macropores. As the mass ratio of ionic liquid to salt eutectics drops from 55% to 15%, that is, the content of salt eutectics increases, the salt eutectics gradually aggregate from ion pairs, to clusters with minimal free energy, and finally to a continuous salt phase, leading to the formation of micropores, uniform mesopores, and macropores, respectively; these processes cause BET specific surface area initially to increase but subsequently to decrease. With the mass ratio of ionic liquids to salts at 35% and carbonization temperature at $900^{\circ}C$, the specific surface area of the resultant carbon aerogels reached $2309m^2g^{-1}$. By controlling the carbonization temperature and mass ratio of the raw materials, the hierarchically porous architecture of carbon aerogels can be tuned; this advantage will promote their use in the fields of electrodes and adsorption.

• 생물환경조절학회지
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• 제12권2호
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• pp.68-71
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• 2003

풋고추의 육묘관리시에 최적 시비농도를 구명하기 위하여 무기이온을 농도별로 처리한 다음 식물체의 생육과 광합성에 미치는 효과를 조사하였다. 초장은 무기이온의 농도가 증가할수록 길었으며, 표준농도인 1.0배를 시비한 것보다 2.0배의 고농도로 시비하였을 때에 ‘녹광’은 72%, ‘꽈리’는 18% 신장생장이 촉진되었다. 건물중은 ‘꽈리’의 경우에 무기이온의 농도가 높을수록 증가하였으나, ‘녹광’의 경우에는 고농도인 2.0배 처리시에는 오히려 감소하였다. 엽록소의 함량은 무기이온의 농도가 2.0배까지 높을수록 증가하였다 광합성속도, 기공전도도 및 증산속도는 두 품종 모두 1.5배의 농도로 관주하였을 때에 가장 높았는데, 이때의 광합성속도를 비교하면 ‘녹광’은 8.74$\mu$mol$.$m$^{-2}$ s$^{-1}$, ‘꽈리’는 5.10$\mu$mol$.$m$^{-2}$ s$^{-1}$로서 생육이 왕성하였던 ‘녹광’의 광합성속도가 더 높았다.

• 멤브레인
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• 제13권1호
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• pp.29-36
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• 2003

A characterization of the permeation and separation using single salt solution was carried out with charged composite membranes. Various charged composite membranes were fabricated by blending an ionic polymer with a nonionic polymer in different ratios. In this study, sodium alginate, chitosan and poly(vinyl alcohol) were employed as anionic, cationic and nonionic polymers, respectively. The permeation and separation behaviors of the aqueous salt solutions have been investigated through the charged composite membranes with various charge densities. As the content of the ionic polymer increased in the membrane, the hydrophilicity of the membrane increased, and pure water flux and the solution flux increased correspondingly, indicating that the permeation performance through the membrane is determined mainly by its hydrophilicity. Electrostatic interaction between the charged membrane and ionic solute molecules, that is, Donnan exclusion, was observed to be attributed to salt rejection to a greater extent, and molecular sieve mechanism was effective for the separation of salts under a similar electrostatic circumstance of solutes.

• 공업화학
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• 제31권3호
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• pp.305-309
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• 2020

본 연구에서는 에테르가 기능화된 이온성 액체인 [DMIm][MPEGP] (1,3-dimethylimidazolium (2-methoxy(2-ethoxy(2-ethoxy)))-ethylphosphite)와 리튬염인 LiTf₂N (lithium bis(trifluoromethanesulfonyl)imide)을 혼합하였고, 리튬염의 함량을 조절하여 전해질을 특성을 조사하였다. 제조된 전해질은 리튬염 혼합에 따라 불투명해지고 흐름성이 제한된 열방성 액정을 형성하였으며, 이때 리튬염의 함량에 따라 형성되는 이온성 액정의 자기조립구조와 이온 전도 현상을 다양한 분광학적 분석을 통해 조사하였다. 그 결과 이온성 액정의 향상된 이온전도도는 정렬된 구조를 통한 이온 전도 특성과 관계가 있음을 확인하였으며, 리튬이온전지 특성 평가에서 우수한 전기화학적 특성을 나타냄을 확인하였다.

• 한국응용과학기술학회지
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• 제25권4호
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• pp.469-476
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• 2008

The synthesis of cyclic carbonate from butyl glycidyl ether (BGE) and carbon dioxide was performed in the presence of three different types of ionic liquid : quarternary ammonium salt, alkyl pyridinium salt, and alkylimidazolium salt. Ionic liquids of different alkyl groups ($C_3$, $C_4$, $C_6$ and $C_8$) and anions ($Cl^-$, $Br^-$ and $I^-$) were used for the reaction which was carried out in a batch autoclave reactor at $60{\sim}120^{\circ}C$. The catalytic activity was increased with increasing alkyl chain length in the order of $C_3$ < $C_4$ < $C_6$. But the ionic liquid with longer alkyl chain length ($C_8$) decreased the conversion of BGE because it is too bulky to form an intermediate with BGE. For the counter anion of the ionic liquid catalysts, the BGE conversion decreased in the order $Cl^-$ > $Br^-$ > $I^-$.

• 멤브레인
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• 제11권1호
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• pp.22-28
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• 2001

이온성 고분자에 비이온성 고분자를 섞어 이온 함량을 조절함으로써 다양한 전하량을 갖는 이온성 막을 제조하였다. 비이온성 고분자로는 폴리비닐알콜, 음이온성 고분자로는 알긴산 나트륨, 양이온성 고분자로는 키토산을 사용하였으며, 이들 이온성 고분자막을 사용하여 여러 전해질 수용액에 대한 투과 및 분리특성을 관찰하였다. 막 내부에 이온성 고분자 함량이 많을수록 친수성 특성을 보였으며, 순수투과 및 용액투과 속도가 증가함을 관찰할 수 있었고, 또한 투과속도는 막의 팽윤 거동에 의해 결정됨을 확인할 수 있었다. 용질 배제율의 경우는 막과 투과용질간의 정전기적 인력, 즉 Donnan exclusion에 의해 결정이 되며, 정전기적 인력이 비슷한 경우는 분자체 효과에 의해 분리됨이 관찰되었다.

• Bulletin of the Korean Chemical Society
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• 제32권8호
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• pp.2633-2636
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• 2011

A new type of ionic liquid based on N-(3-aminepropyl)imidazolium iodide, called IIQAI, which consists of imidazolium and quaternary ammonium salt, and APII-(hydroxyethyl, propyl, hexyl) were synthesized and used as ionic liquid in dye-sensitized solar cells. APII-hexyl is solid, whereas IIQAI, APII-(hydroxyethyl, propyl) are viscous liquids. The synthesized ionic liquid showed relative thermal stability compared to the commercial ionic liquid of DMII. Among them, IIQAI was more stable than the other ionic liquid because of the two salt groups. APII-hydroxyethyl, which contains two hydroxyl groups, showed low viscosity with good flow. New types of ionic liquids were examined by $^1H$-NMR spectroscopy, thermo gravimetric analysis (TGA). IIQAI enabled a solar energy conversion efficiency of 6.3%, which is slightly higher than that of the referenced (DMII, 6.2%).

• 폴리머
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• 제32권5호
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• pp.409-414
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• 2008

전기방사법으로 이온염을 함유하는 TFE/증류수 혼합용매를 이용하여 젤라틴 나노섬유를 제조하였으며, 얻어진 나노섬유의 평균직경은 $110{\sim}125\;nm$였다. 이온염의 농도가 증가할수록 비드의 발생이 줄어들고 균일한 나노섬유 제조가 가능하였다. 이는 이온염의 첨가에 의한 젤라틴 용액의 점도 및 전도도가 증가함에 기인하는 것으로 확인되었다. 특히 일가이온보다 이가이온을 사용할 경우 점도 및 전도도의 증가에 더 효과적이었으며 이들 이온염은 분자간 소수성 상호작용뿐만 아니라 젤라틴 분자의 입체구조 정렬에도 영향을 주었다. 그러나 이온염 농도에 따른 나노섬유의 직경변화는 관찰되지 않았다. 제조된 나노섬유를 이용한 XRD분석 결과 이온염의 농도가 증가할수록 젤라틴 분자의 재결정화에 의해 나노섬유의 결정화도가 높아졌다.

• Biotechnology and Bioprocess Engineering:BBE
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• 제6권1호
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• pp.37-41
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• 2001

HPLC separation of ionic samples tends to be more complicated and difficult to understand than that of non-ionic compounds. On the other hand, band spacing is much more easily manipulated for ionic than for neutral samples. Ion-suppression RP-HPLC method was used with organic modifier and aqueous buffer solution. In this work, five mononucleotides of cytidine-5-monophosphate (5-CMP) disodium salt, uridine-5-monophosphate disodium salt (5-UMP), guanosine-5-monophosphate disodium salt (5-GMP), inosine-5-monophosphate disodium salt (5-IMP), and adenosine-5-monophosphate disodium salt (5-AMP) were examined. Acetic acid and sodium phosphate were used as buffers, and methanol as an organic modifier. A new relationship between the retention factor and the buffer concentration at a fixed modifier content (5% of methanol) could be expressed by following: K = (k(sub)-1 + k(sub)0 (k(sub)B/k(sub)S)/(1 + (k(sub)B/k(sub)S) C(sub)B(sup)a), where C(sub)B was the concentration of buffer. Using this relationship, the calculated values closely matched the experimental data. The derived relationship showed that as the buffer concentration increased, the retention factor approached a certain value, and this was buffer dependent.