• Journal of Electrochemical Science and Technology
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• 제2권2호
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• pp.63-67
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• 2011

To examine the effects of a two-cation ionic liquid as an electrolyte component of a supercapacitor, 1,4-bis(3-methylimidazolium-1-yl)butane tetrafluoroborate ($MIBBF_4$), dissolved in propylene carbonate (PC) or acetonitrile (ACN), is newly synthesized and tested here for potential use as an electrolyte of capacitor. The $MIBBF_4$ salt exhibits higher ionic conductivity in ACN than in PC. The supercapacitive properties of capacitors containing an activated carbon electrode and various electrolytes are evaluated using cyclic voltammetry and electrochemical impedance spectroscopy. The capacitor adopting the $MIBBF_4$/ACN electrolyte shows the largest specific capacitance at low scan rates, whereas the capacitor adopting the 1-ethyl-3-methylimidazolium tetrafluoroborate $(EMIBF_4)$/ACN electrolyte shows the largest specific capacitance at high scan rates.

• Membrane and Water Treatment
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• 제4권3호
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• pp.203-214
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• 2013

Laboratory tests were performed to determine the efficiency of dye solution desalination by electrodialysis. The study involved anionic dye and mineral salt recovery by obtaining two streams from a salt and dye mixture - dye-rich solution and salt solution. A standard anion-exchange and cation-exchange membranes or monovalent selective anion-exchange membranes were used in the ED stack. It was found that the separation efficiency was strongly dependent on the dye molecular weight. The best results for standard ion-exchange membranes were achieved for the desalination of Direct Black solution. Furthermore, the obtained results implied that the application of monovalent selective anion-exchange membranes improved the recovery of dye and salt solutions - the dye concentration in the diluate remained constant irrespective of the molecular weight of anionic dyes, whereas the salt recovery remained very high (99.5%).

• 전기화학회지
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• 제18권1호
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• pp.24-30
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• 2015

일반적으로 저농도의 염 용액에서 탈염성능이 우수한 축전식 탈염기술에 고농도의 염을 함유한 용액을 처리할 수 있는 가능성을 확인하기 위해 spacer와 spiral 형태의 두 가지 모양의 유로에따라 이온교환수지를 채움으로써 탈염효율을 비교분석하고 기술의 적용가능성을 평가하였다. Spacer와 spiral 형태로 이온교환수지를 채운 축전식 탈염 셀의 탈염효율은 각각 77.21 및 99.94%로, 이는 spiral 형태의 유로에 채워진 이온교환수지가 유입수와 고르게 접촉할 수 있는 유로의 모양을 구성하기 때문에 많은 이온들이 제거될 수 있었다고 판단된다. 또한 pH와 축적 전하량의 변화량에서 탈염성능을 감소시킬 수 있는 페러데이 반응이 현저하게 줄어들었다. 따라서 본 연구를 통해 에너지효율적인 축전식 탈염 기술을 이용하여 고농도의 염 용액의 탈염에 대한 가능성을 제시해주었고, 이온교환수지의 혼합비율의 최적화와 연속식 전기탈이온 기술의 재생공정의 도입에 대한 추가적인 연구를 통해 이상적인 탈염기술을 개발하는 데 큰 기반이 될 것으로 기대된다.

• 한국대기환경학회지
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• 제15권4호
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• pp.385-392
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• 1999

This study was carried out to investigate the constituents of inorganic ions of precipitation in Mokpo and Yeochon area from Jan. 1996 to Dec. 1997. The volume-weighted mean pH of precipitation was 5.7(4.8~7.8) at Mokpo, and 5.6(5.1~7.4) at Yeochon area, respectively. The non-seasalt(nss) anion concentrations were found in order of $nss-SO^{2-}_4>NO^-_3>nss-Cl^-$ at two areas. The portion of $nss-SO^{2-}_4;and;NO^-_3$ was 71~84% out of anions. The the non-seasalt cation concentrations were found in order of $NH^+_4>nss-Ca^{2-}>nss-Mg^{2+}>nss-K^-$ at two areas. The portion of $NH^+_4;and; nss-Ca^{2+}$ was 85~92% out cations. Compared regionally the year concentraton of $nss-SO^{2-}_4$, the result of Yeochon was 3 times higher than that of Mokpo in 1996, while the results of two regions were almost similar in 1997. The reason was that Yeochon was restricted area of the use of 0.5% sulfur B-C oil, controlled air pollution emission area, controlled semitotal amounts of air pollution emission area and partial operating of factories in 1997. There were no ions having high correlation with $H^+,;but;nss-SO^{2-}_4,;NO^-_3,;NH^+_4;and;nss-Ca^{2+}$ showed high correlation coefficient each other. It seems that these ions have little correlation with $H^+$ because they are washed out on binding state. Factor analysis showed that the first factor was complicated factor containing anthropogenic and soil resource, the second factor was sea-salt resource and the third factor was independent behavior of hydrogen at Mokpo. While, the first factor was complicated factor containing anthropogenic and sea-salt resource, the second factor was $Ca(NO_3)_2$ salt and the third factor was $NH^+_4;and;SO^{2-}_4$ synergied by resource and combination at Yeochon.

• 공업화학
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• 제21권1호
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• pp.87-92
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• 2010

탄소전극으로만 구성된 단위 셀(CDI)과 음극 표면에 양이온교환막을 결합한 단위 셀(MCDI)을 제작하여 탈염실험을 수행하였다. 실험결과 탈염속도와 탈염량은 셀 전위가 증가할수록 선형적으로 증가하였다. 그러나 동일한 탄소전극을 사용했음에도 불구하고 MCDI 셀이 CDI 셀보다 높은 탈염효율을 보였다. 셀 전위를 0.8~1.2 V로 변화시키면서 실험한 결과 흡착량은 셀 전위에 따라 MCDI 셀이 CDI 셀보다 33.1~135% 정도 증가하는 것으로 나타났다. 또한 전류효율에서도 MCDI 셀은 80% 정도를 나타낸 반면 CDI 셀은 40% 이하의 전류효율을 나타내었다. MCDI 셀에서 탈염효율이 높은 원인은 흡착 및 탈착전위가 인가되었을 때 전극 표면의 전기이중층과 bulk 용액 사이에서 이온들이 선택적으로 이동하기 때문인 것으로 사료된다.

• Bulletin of the Korean Chemical Society
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• 제25권11호
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• pp.1635-1640
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• 2004

The cyclophanes 1a-d containing two benzo[b]furan rings connected by various bridges have been prepared and their binding behaviors with N-benzylphenethylammonium cation 2 were examined by NMR titration method. The successive alkylation reactions of 4-hydroxyl groups and then 2-hydroxyl groups of 2,4-dihydroxybenzophenonse gave macrocycles 5a-c. Photoirradiation of the macrocycles 5a-c with 350 nm mercury lamp followed by dehydration afforded the cyclophanes 1a-c. Hydrolysis of two ester groups pendant on a bridge of 1b produced the carboxyl group-containing cyclophane 1d. The cyclophane 1a having a p-xylene bridge showed 1 : 1 binding with 2 with the binding constant of $36{\pm}6M^{-1}$ in 3 : 1 $CDCl_3$/methanol-$d_4$ solvent, while 1b and 1c which have neutral flexible bridges exhibited no appreciable binding with 2. The disodium salt of 1d showed much higher binding affinity for 2 forming 1 : 1 and 1 : 2 complexes.

• Nuclear Engineering and Technology
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• 제12권2호
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• pp.99-105
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• 1980

과망간산염, 염소산염및 과염소산염의 중성자 포획에 수반하는 망간-56 및 염소-38 반조화학종의 분배를 이온교환크로마토구라휘법으로 검토하였다. 과망산염의 망간-56 방사능은 2종의 원자가상태로 나타나며 염소산염의 염소-38은 2종의 원자가상태 그리고 과염소산염의 염소-38은 3종의 원자가상태로 나타난다. 반조에너지는 계산하였다. $^{38m}$Cl의 핵이성체 전이에 수반하는 내부전환은 잔류율에 영향을 미친다. 양이온반경이 클수록 2차 케이지를 돌파하는 반조원자의 확율이 높다. 암모늄염중 암모늄이온은 환원제 작용을 한다. 결정구조에서 자유공간이 크면 잔류율은 낮아진다.다.

• 통합자연과학논문집
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• 제10권3호
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• pp.131-136
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• 2017

The chemical shifts in the $^{13}C$ NMR spectra of 2,3,4,5-tetraphenyl-1-silacyclopentdienide dianion $[SiC_4Ph_4]^{2-}{\cdot}2[K^+]$ (3) and 2,3,4,5-tetraphenyl-1-germacyclopentdienide dianion $[GeC_4Ph_4]^{2-}{\cdot}2[K^+]$ (4) were compared to those of $[SiC_4Ph_4]^{2-}{\cdot}2[Li^+]$ (5), $[SiC_4Ph_4]^{2-}{\cdot}2[Na^+]$ (6), and $[GeC_4Ph_4]^{2-}{\cdot}2[Li^+]$ (7). The average polarizations in two phenyl groups of two potassium salts are decreased over 15% to 20% comparing to those of the lithium salts and sodium salt {$[EC_4Ph_4]^{2-}{\cdot}2[M^+]$ (E=Si, Ge, M=Li, Na) due to the effect of the counter potassium cation.

• 대한핵의학회지
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• 제28권3호
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• pp.331-337
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• 1994

In order to develop a $^{18}F$-labelled myocardial perfusion agent(flow tracer) for PET, $^{18}F$-labelled organic ammonium cations were synthesized and evaluated in relation to their biodistribution. Five quaternary organic ammonium compounds were labelled with $^{18}F$ in a side chain with moderate to good yields by direct introduction of $^{18}F$-fluoride. Radiochemical yields have been achieved in 30-40min by the precursors (tosylates) in dimethylsulfoxide 15-60% (decay corrected). The reaction was found to be autocatalyzed. A remote controlled procedure was developed in these synthesis. $^{18}F$-Labelling and HPLC-purification of com-pounds needed about 60 min(Yield; 7-20%). Up to now the two compounds N-4-[$^{18}F$]fluorobutyl-pyridinium cation(1) and N, N dibenzyl-4(2-[$^{18}F$]fluoroethyl)piperidinium cation(2) were investigated in relation to their biodistribution in mice. Compound 1 showed at 1 min post injection the high uptake of 19.22% ID/g organ in the myocardium but a following fast decline to 1.12% ID/g organ after 40min. Uptake of compound 2 was after 1min in the heart 5.90% ID/g organ but after 40min at the relative high value of 4.33% ID/g organ. Heart:blood ratio for compound(1) at 1 min was 8.3, at 40 min 2.6 for compound II 2.0(1min) and 15.0(40 min). As data of compound 2 showed greater heart uptake, slower myocardial release, and higher heart: blood ratios, compound 2 is a good candidate for further evaluation.

• 대한화학회지
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• 제42권6호
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• pp.696-702
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• 1998

황피독에 저항성을 가지는 수성가스 전환반응용 CoMo 계열 촉매에 알칼리금속염 첨가가 반응활성에 미치는 영향에 대하여 연구하였다. 알칼리금속염의 음이온과 양이온의 각각에 대한 영향을 알아보기 위하여 크게 두 경우로 나누어 촉매를 제조하였다. 그 하나는, 양이온을 K로 고정시키고 음이온을 변형시킨 경우로서, 반응활성의 변화는 BET 표면적의 변화로 설명되었다. 다른 한 경우는, 음이온을 $NO_3^-$로 고정시키고 알칼리금속 이온을 변형시킨 경우로서, Li가 첨가된 촉매의 활성이 가장 뛰어났으며 다른 양이온의 경우에는 서로 비슷한 낮은 활성을 보였다. 알칼리금속의 첨가량의 변화에 따른 BET 표면적의 변화와 반응활성의 변화가 같은 경향을 보였다. 알칼리금속염의 양이온을 변화시킨 경우에는 BET 표면적과 정8면체 배위구조 속의 $Mo^{6+}$에 대한 정4면체 배위구조 속의 $Mo^{6+}$의 비, 즉 $Mo^6+[T]/Mo^{6+}[O]$ 값의 복합적인 관계를 통해 반응활성의 변화를 설명할 수 있었다.