• Applied Chemistry for Engineering
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• v.9 no.1
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• pp.38-43
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• 1998

It was realized that the nucleation rate in the synthesis of M-ZSM-5 using various alkali cations such as $Li^+$, $Na^+$, $K^+$ and $Cs^+$ at low temperature and atmospheric pressure was decreased in the order of $Na^+>K^+>Li^+>Cs^+$. Unlike conventional synthesis method at high temperature and pressure, the results showed that at low temperature and atmospheric pressure, the higher the nucleation rate is, the larger the crystal size of M-ZSM-5 obtained ; that is, the crystal size in the order of $K^+>Na^+>Cs^+>Li^+$. In addition, it also suggests that regardless of alkali cations to be used, the current synthesis method can produce M-ZSM-5 with BET surface area greater than $300m^2/g$ within 52hrs. of reaction time, in particular greater than $400m^2/g$ within 32hrs, for $Na^+$ cation.

• Journal of the Korean Chemical Society
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• v.27 no.3
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• pp.208-212
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• 1983

The stability constants for the complexes formed between dibenzo-18-crown-6 compound and alkaline earth metal cations in dimethylsulfoxide, dimethylformamide, and acetonitrile have been obtained by conductometry at $25{\circ}C\;and\;35{\circ}C$respectively. The stability constants were increased in order of $Ca^{2+} in any solvent, and the magnitudes were found to be reversely proportional to the solvent donicities. The result could be understood in terms of ion-cavity radius concept, solvent basicity, and solvation of the cations.

• Applied Chemistry for Engineering
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• v.19 no.5
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• pp.533-538
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• 2008

In order to enhance the adsorption capacity of $CO_2$, a commercial zeolite and coal fly ash were chemically modified with alkali cations (Li, K) and alkaline-earth cations (Ca, Mg). Adsorbents containing Ca and Mg showed slightly lower surface areas. The adsorption capacity at the ambient temperature was highest with Ca, then in order of Mg, Li, and K. On the contrary, regeneration efficiency of the adsorbents with Ca and Mg was relatively low, because Ca and Mg cations had stronger affinity of carbon dioxide. The affinity between cations and $CO_2$ molecule also may improve the selectivity in favor of $CO_2$ adsorption.

• Journal of the Korean Electrochemical Society
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• v.9 no.3
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• pp.132-134
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• 2006

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 tetracycline used as neutral carriers for cation selective polymeric membrane electrode was investigated. The cation ion-selective electrode based on tetracycline gave a good Nernstian response of 26.6 mV per decade for calcium ion in the activity range $1x10^{-6}M$ to $1x10^{-2}M$ with and without lipophilic additives. The optimized cation ion-selective membrane electrodes displayed very comparable potentiometric responses to various mono and di-valent cations of alkali and alkaline earth metal ions except $Mg^{2+}$.

• Journal of the Korean Chemical Society
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• v.45 no.1
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• pp.31-39
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• 2001

Newly synthesized 15-Crown-5 derivatives including anthracene were used as neutral carriers for ion selective electrodes to determine potassium ion by potentiometry. Among the five neutral carriers studied in this work, N-(4'-benzo-15-crown-5-ether)-anthracene-9-imine was found to be the best in terms of selectivity and stability. The optimal composition of ion selective membrane was 1.0, 33.0 and 66.0 wt% for neutral carrier, PVC and plasticizer, resperctively. Addition of KTpCIPB used as a lipophilic additive improved the Nernst slope and the selectivity of potassium ion over alkali and alkaline earth metals. Especially, the selectivity of potassium ion over ammonium ion was remarkably good ($logK^{pot}_(K^+,NH_4^+}$=-2.59). The response time was also excellent ($t_{100}$=5sec) and continuous use of this electrode for three weeks has not changed the selectivity and analytical characteristics.

• Journal of the Korea Institute of Building Construction
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• v.16 no.4
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• pp.321-329
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• 2016

The use of ternary blended cement consisting of Portland cement, granulated blast-furnace slag (GGBFS) and fly ash has been on the rise to improve marine concrete structure's resistance to chloride attack. Therefore, this study attempted to investigate changes in chloride attack resistibility of concrete through NT Build 492-based chloride migration experiments and test of concrete's ability to resist chloride ion penetration under ASTM C 1202(KS F 2271) when 1.5-2.0% of alkali-sulfate activator (modified alkali sulfate type) was added to the ternary blended cement mixtures (40% ordinary Portland cement + 40% GGBFS + 20% fly ash). Then, the results found the followings: Even though the slump for the plain concrete slightly declined depending on the use of the alkali-sulfate activator, compressive strength from day 2 to day 7 improved by 17-42%. In addition, the coefficient from non-steady-state migration experiments for the plain concrete measured at day 28 decreased by 36-56% depending on the use of alkali-sulfate. Furthermore, total charge passed according to the test for electrical indication of concrete's ability to resist chloride ion penetration decreased by 33-62% at day 7 and by 31-48% at day 28. As confirmed in previous studies, reactivity in the GGBFS and fly ash improved because of alkali activation. As a result, concrete strength increased due to reduced total porosity.

• Journal of the Korean Chemical Society
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• v.30 no.4
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• pp.359-368
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• 1986

Solvent extraction equilibria of alkali metal cation with crown ether (DC18C6, DC24C8) and HDEHP have been studied. The extraction equilibrium constants increase in the order of, in the DC18C6 system, $Na^+, and in the DC24C8 system, $Rb^+. The species extracted to organic phase are $M_1(crown ether)_1\;(HDEHP)_1$. The magnitude of extraction equilibrium constant is determined by the distribution ratio of crown ether between organic and aqueous phase, and stability constant of crown ether-alkali metal complex.

• Journal of the Korean Wood Science and Technology
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• v.10 no.4
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• pp.67-75
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• 1982

모텔리그닌의 펄프화(化) 처리(處理) 및 폐액(廢液)리그닌의 반응생성물(反應生成物)로부터 알칼리 및 설페이트 펄프화중(化中)에 일어나는 반응양식(反應樣式)을 조사(調査)한 것이다. 알칼리의 처리결과(處理結果)는 친핵시약(親核試藥)에 의해 페놀레이트 이온이 생성(生成), 퀴논메타이드 중간체(中間體)를 걸쳐 $C_6-C_3$ 단위(單位)의 ${\alpha}$위(位) aryl은 탈리(脫離)하여, 리그닌은 저분자화(低分子化)가 시작되고, 저분자생성물(低分子生成物)은 축합반응(縮合反應)에 의해 극(極)히 일부(一部)는 고분자화(高分子化)된다. 저분자화(低分子化)된 리그닌은 산화(酸化)에 의해 퀴노이드 착색구조(着色構造)를 형성(形成)한다. 페놀성의 일부(一部) 및 비(非)페놀성리그닌은 oxirane와 thiirane의 중간체(中間體)를 거쳐 $C_6-C_3$ 단위(單位)의 ${\beta}$위(位)의 arylether가 탈리(脫離)된다. 그러나, hydrosulfide 이온은 hydroxide 이용 보다 강(强한)한 친핵종(親核種)이므로 thiirane의 중간체(中間體) 생성(生成)이 용량(容量)하여 개열(開裂)이 더욱 촉진(促進)된다. 저분자(低分子)리그닌의 고분자축합(高分子縮合)은 벤젠핵(核)의 2.6 위(位)보다 5위(位)에 축합(縮合)이 많이 일어 난다.

• Journal of the Korean Chemical Society
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• v.44 no.2
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• pp.115-119
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• 2000

A PVC membrane electrode based on upper-rim calix[4] crown as ionophore was prepared using dioctyl sebacate (DOS) as a plasticizer. The potential response of this membrane electrode to alkali, alka-line earth and transitionmetal metal cations were examined. This membrane electrode exhibited a Nernstian response to $10^{-6}{\sim}10^{-2}M\;Pb(NO_3)_2$ with a slope ot 27.0 mV/decade. Its response time ($t_{90}$) was 10s and it could be used for at least 2 months. Also, the potential was maintained constantly in the rage of ph $2.0{\sim}12$.

• Journal of the Korean Chemical Society
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• v.42 no.5
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• pp.531-538
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• 1998

The ion selective membrane electrode made of calix[4]arene-based host 1 as ionophore, poly (vinyl chloride) (PVC) as matrix and dioctylsebacate (DOS) as a plasticizer was studied. The potential responses of this membrane electrode to alkali, alkaline earth and transition metal cations were investigated. Especially this membrane electrode was turned out to be affinitive for $Pb^{2+}$ in the deionized water. It was observed that the response was linear in the concentration range from $1.0 \times 10^{-1} M to 1.0 \times 10^{-6} M of Pb^{2+}$ and its slope (26.5 mV/decade) was near to the sub-Nernstian response in deionized water. Also, the potential was maintained constantly in the range of pH $4.00 \sim 12.00$, which supports the potential usage as $Pb^{2+}$ affinitive electrode in the deionized water.