• 분석과학
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• 제8권4호
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• pp.793-798
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• 1995

A new chromoionophore sym-(decyl)(2-hydroxy-5-nitrobenzyloxy)-dibenzo-16-crown-5 (1) has been synthesized for $Na^+$ photometry in aqueous media. Apparent $pK_a$ values of 1 in the presence of 0.10 M LiCl, NaCl, and KCl were measured by spectrophotometry in 50% 1,4-dioxane-50% water (v/v) and compared with the $pK_a$ of 8.68 in the presence of 0.10 M TMACl. A significant $pK_a$ shift to a lower pH was only observed for $Na^+$ (${\Delta}pH=1.31$) due to selective binding of 1 with $Na^+$. Based upon this $pK_a$ shift, chromoionophore 1 was found to selectively respond to $Na^+$ with a detection limit of $10^{-3}M$ and no interference from $K^+$ up to 0.05 M for detection of 10.0 mM $Na^+$ in 50% 1,4-dioxane-50% water (v/v).

• Korean Chemical Engineering Research
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• 제55권5호
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• pp.718-722
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• 2017

마이크로파 공정으로 제조된 순수한 $LaCoO_3$와 금속이온이 첨가된 $LaCoO_3$ 페롭스카이트 산화물에서 메틸오렌지의 광촉매 분해반응의 활성을 조사하였다. 순수한 $LaCoO_3$와 세슘 이온이 첨가된 $LaCoO_3$ 산화물들은 제조법과 무관하게 페롭스카이트 구조를 보여주었다. UV-Vis DRS 결과에 의하면 모든 촉매들은 가시광 영역에서 흡수스펙트럼을 나타내었다. 화학흡착된 산소종은 메틸오렌지의 광촉매 분해반응에서 중요한 역할을 하였으며, 화학흡착된 산소의 비율이 높을수록 더 높은 광촉매 활성을 보여주었다.

• Bulletin of the Korean Chemical Society
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• 제23권8호
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• pp.1085-1088
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• 2002

Calix[6]arene having both carboxylic acid (1,3,5-) and carboxamide (2,4,6-) in an alternative way was synthesized. Transport rates of alkali and alkaline-earth metal ions were tested in bulk liquid membrane and polymer inclusion membrane. Ba2+ ion was found to give the highest transport rate among tested metal ions in both BLM and PIM systems. In PIM system, high durability (longer than 30 days) of the membrane was observed.

• 분석과학
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• 제8권2호
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• pp.187-193
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• 1995

N,N,N,N-Tetrabenzylethylenediamine 중성운반체를 이용하여 PVC 수소이온 선택성 막전극을 제조하였다. 가소제 종류(phthalates와 sebacate) 및 친지방성 첨가제(NaTPB)에 따른 막전극의 전기저항과 수소이온 감응범위 및 알칼리금속과 알칼리토금속의 존재하에서 방해효과를 조사하였다. 가소제 종류에 의한 전기저항은 영향을 거의 받지 않았고 NaTPB 0.7%의 경우 수소이온에 대한 Nernstian 기울기는 가장 이론값에 근접하였으며, 또한 알칼리금속 및 알칼리토금속에 의한 방해도 적게 받았다. pH-선택성 고분자 막전극은 pH 2~10 범위내에서 선형적이고, 산과 알칼리용액 중에서 안정성 및 재현성 시험 결과 매우 좋게 나타났다.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2007년도 추계학술대회 논문집
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• pp.292-292
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• 2007

To apply PDP panel, Soda lime glass(SLG) is cheeper than Non-alkali glass and PD-200 glass but has problems such as low strain temperature and ion diffusion by alkali metal oxide. In this paper suggest the methode that prohibits ion diffusion by deposing barrier layer on SLG. Indium thin oxide(ITO) thin films and barrier layers were prepared on SLG substrate by Rf-magnetron sputtering. These films show a high electrical resistivity and rough uniformity as compared with PD-200 glass due to the alkali ion from the SLG on diffuse to the ITO film by the heat treatment. However these properties can be improved by introducing a barrier layer of $SiO_2\;or\;Al_2O_3$ between ITO film and SLG substrate. The characteristics of films were examined by the 4-point probe, SEM, UV-VIS spectrometer, and X-ray diffraction. GDS analysis confirmed that barrier layer inhibited Na and Ka ion diffusion from SLG. Especially ITO films deposited on the $Al_2O_3$ barrier layer had higher properties than those deposited on the $SiO_2$ barrier layer.

• 분석과학
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• 제18권6호
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• pp.491-494
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• 2005

The main component governing selectivity in ion-selective electrodes and optodes is the ionophore. For this reason, a member of natural products that possess selective ion-binding properties have long been sought after. By applying this principle, the performance of cyclosporin used as neutral carriers for calcium selective polymeric membrane electrode was investigated. The calcium ion-selective electrode based on cyclosporin gave a good Nernstian response of 26.6 mV per decade for calcium ion in the activity range $1{\times}10^{-6}M$ to $1{\times}10^{-2}M$. The optimized calcium ion-selective electrode displayed very comparable selectivity for $Ca^{2+}$ ion against alkali and alkaline earth metal ions, $Na^{2+}$, and $Mg^{2+}$ in particular.

• Bulletin of the Korean Chemical Society
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• 제35권6호
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• pp.1789-1793
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• 2014

Pseudo-first-order rate constants ($k_{obsd}$) have been measured spectrophotometrically for the reactions of 5-nitro-8-quinolyl nicotinate (4) and 5-nitro-8-quinolyl isonicotinate (5) with alkali metal ethoxides (EtOM; M = K, Na and Li) in anhydrous ethanol at $25.0{\pm}0.1^{\circ}C$. The plots of $k_{obsd}$ vs. [EtOM] curve slightly upward for the reactions with EtOK and EtONa but are linear for the reactions with EtOLi and for those with EtOK in the presence of 18-crown-6-ether. Dissection of $k_{obsd}$ into $k_{EtO^-}$ and $k_{EtOM}$ (i.e., the second-order rate constants for the reactions with the dissociated $EtO^-$ and ion-paired EtOM, respectively) has revealed that the reactivity increases in the order $EtO^-{\approx}EtOLi$ < EtOK < EtONa for the reactions of 4 and EtOLi < $EtO^-$ < EtOK < EtONa for the reactions of 5. Comparison of the kinetic results for the reactions of 4 and 5 with those reported previously for the corresponding reactions of 5-nitro-8-quinolyl benzoate (2) and picolinate (3) has revealed that the esters possessing a pyridine ring (i.e., 3-5) are significantly more reactive than the benzoate ester 2 due to the presence of the electronegative N atom (e.g., 2 << 3 < 4 < 5). It has been concluded that $M^+$ ion catalyzes the reactions of 3-5 by increasing the electrophilicity of the reaction center through a five-membered cyclic transition state (TS) for the reaction of 3 and via a four-membered cyclic TS for the reactions of 4 and 5.

• Bulletin of the Korean Chemical Society
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• 제31권10호
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• pp.2929-2933
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• 2010

Pseudo-first-order rate constants ($k_{obsd}$) have been measured for nucleophilic substitution reactions of 2-pyridyl benzoate 5 with alkali metal ethoxides (EtOM, M = Li, Na, K) in anhydrous ethanol. The plots of $k_{obsd}$ vs. $[EtOM]_o$ are curved upwardly but linear in the excess presence of 18-crown-6-ether (18C6) with significant decreased $k_{obsd}$ values in the reaction with EtOK. The $k_{obsd}$ value for the reaction of 5 with a given EtONa concentration decreases steeply upon addition of 15-crown-5-ether (15C5) to the reaction medium up to ca. [15C5]/$[EtONa]_o$ = 1, and remains nearly constant thereafter, indicating that $M^+$ ions catalyze the reaction in the absence of the complexing agents. Dissection $k_{obsd}$ into $k_{EtO^-}$- and $k_{EtOM}$, i.e., the second-order rate constants for the reaction with the dissociated $EtO^-$ and the ion-paired EtOM, respectively has revealed that ion-paired EtOM is 3.2 - 4.6 times more reactive than dissociated $EtO^-$. It has been concluded that $M^+$ ions increase the electrophilicity of the reaction center through a 6-membered cyclic transition state. This idea has been examined from the corresponding reactions of 4-pyridyl benzoate 6, which cannot form such a 6-membered cyclic transition state.

• 대한기계학회논문집A
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• 제41권7호
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• pp.665-671
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• 2017

알칼리금속을 이용한 열전기변환장치(Alkali-Metal Thermal-to-electric Converter)는 열을 전기로 직접 변환하는 기술이다. AMTEC 기술은 기존 에너지기술 대비 고효율성과 고밀도성을 지니는 정적 에너지 변환 장치로서 이론 발전효율이 40%로 높고 단위발전량이 500 W/kg, $2.01W/cm^2$로 우수하다. AMTEC의 작동원리는 작동유체인 소듐이 분압차이에 의해서 고체전해질인 베타알루미나(BASE)의 내부에서 외부로 이온화를 거쳐며 통과하는데, 이때 전자를 주고 받으며 전기를 생성한다. BASE내외부의 분압차 형성을 위해서는 고온내구성과 기밀성이 높은 접합기술이 요구된다. 개발된 접합기술을 이용하여BASE/절연부/금속부 시스템의 안정적인 전기적/구조적 시스템을 구성하고 멀티-셀 모듈들을 제작하여 개방회로 전압과 전류-전압특성을 측정하는 방법으로 AMTEC 모듈전지들의 출력성능과 수명을 평가하였다.

• 멤브레인
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• 제33권3호
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• pp.87-93
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• 2023

전기투석(ED)은 이온교환막을 통한 이온의 분리에서 중요한 과정이다. 해수담수화로 발생하는 염수 처리는 환경적으로 큰 문제이며 막분리 기술을 통한 재활용 효율이 높다. 마찬가지로 알칼리는 가죽, 전기도금, 염색, 제련 등과 같은 여러 화학 산업에서 생산된다. 폐기물의 고농도 알칼리는 부식성이 높고 화학적 산소 요구량(COD) 값이 높기 때문에 환경에 방출하기 전에 처리해야 합니다. 칼슘과 마그네슘의 농도는 염수의 거의 두 배이며 주요 환경 오염 물질인 이산화탄소의 흡착에 완벽한 후보입니다. 수산화나트륨은 양극성 막 전기투석 공정으로 쉽게 생산되는 금속 탄산화 공정에 필수적입니다. 역삼투압(RO), 나노여과(NF), 초여과(UF), ED 등 다양한 공정을 통해 회수가 가능하다. 본 검토에서는 알칼리 회수를 위한 이온교환막에 의한 ED 공정에 대해 논의한다.