• Archives of Pharmacal Research
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• 제8권2호
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• pp.91-98
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• 1985

Dependence of the flow behavior of aqueous suspension of Young-Il bentonite on the concentration and the type of electrolytes was studied. Viscosity measurements were made was Rion Viscotester, using No. 3 rotor at 62.5 R. P. M. at 25.deg.C. As electrolyte concentration increased, the apparent viscosity was observed to increase. Changes in viscosity were in general agreement with predicted results based on the Hofmeister sequence and the Schulze-Hardy rule. The observed electrolyte effect on the apparent viscosity was discussed in terms of the Verwey-Overbeek theory.

• Bulletin of the Korean Chemical Society
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• 제20권7호
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• pp.796-800
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• 1999

Three anthrylazacrown ethers in which the anthracene fluorophore π system is separated from the electron donor atoms by one methylene group were synthesized, and their photophysical study was accomplished. These fluorescent compounds showed a maximum fluorescence intensity at pH=5 in aqueous solutions and a decrease in fluorescence intensity upon binding of paramagnetic metal cations (Mn 2+ (d 5 ), Co 2+ (d 7 ), Cu 2+ (d 9 )). The decrease in fluorescence intensity may be attributed to the paramagnetic effect of metal cations to deactivate the excited state by the nonradiative quenching process. The benzylic nitrogen was found to play an important role in changing fluorescence intensity. From the observed linear Stern-Volmer plot and the fluorescence lifetime independence of the presence of metal ions, it was inferred that the chelation enhanced fluorescence quenching (CHEQ) mechanism in the system is a ground state static quenching process. Enhanced fluorescence was also observed when an excess Na + ion was added to the quenched aqueous solution, and it was attributed to cation displacement of a complexed fluorescence quencher.

• Bulletin of the Korean Chemical Society
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• 제18권2호
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• pp.193-197
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• 1997

Theoretical studies on the base-catalyzed deprotonation of 4-phenacylpyridinium cations, R1-CO-CH2-C5H4N-R2, I (R1=YC6H4 -and R2=CH3), and II (R1=C6H5 and R2=CH2C6H4Y) have been carried out with bases, NH3 and XC6H4NH2 using AM1 MO method. The Brψnsted α values are 0.20 and 0.22 and the βB values are 0.62 and 0.61, respectively for cations I and II. The negative Ⅰ (=α-βB) values obtained are in accord with the experimental results in aqueous solution, although the theoretical gas-phase α values for I are somewhat smaller than the experimental values in water due to neglect of solvation effect. It has been stressed that the Brψnsted α is distorted not only by the lag in the resonance and solvation development in the carbanion, but also by the difference in the distance between the anionic center and substituents in the TS and in the product anion.

• 한국토양비료학회지
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• 제19권2호
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• pp.139-145
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• 1986

담배식물이 흡수한 질산태질소가 조직중(組織中)에서 환원 되므로서 양(陽)이온과 음(陰)이온성분간(成分間)의 평형(平衡)에 미치는 영향을 구명하기 위하여 질소원(窒素源)을 달리한 배양액(培養液)으로 재배(栽培)하면서 무기(無機) 양음(陽陰)이온총량차이(總量差異)를 조사하고 질소환원(窒素還元) 및 유기산함량(有機酸含量)의 변화(變化)와 이온총량차이(總量差異)와의 관계(關係)를 검토(檢討)한 결과(結果) 1. $NO_3-N$ 배양액에서 자란 식물은 $NH_4-N$ 배양액의 것보다 양(陽)이온총량(總量)이 높았다. 무기음(無機陰)이온총량(總量)은 $NO_3+NH_4$혼합배양액(混合培養液)에서 가장 높게 나타났으나 $NO_3-N$ 배양액에서 가장 낮아서 무기 양음(陽陰)이온총량차이(總量差異)가 가장 컸고 $NH_4{^+}$가 함유된 배양액에서는 무기양음이온 총량차이가 비슷하여 무기이온으로서 거의 이온균형(均衡)이 유지(維持)되었다. 2. 식물체중(植物體中) 유기산(有機酸)은 malic acid의 분포가 가장 컸으며 $NO_3-N$ 배양액식물은 유기산(有機酸)이 다량함유(多量含有)되어 있으나 $NH_4-N$ 또는 혼합배양액(混合培養液)의 것은 거의 검출(檢出)되지 않았다. $NO_3-N$ 배양액식물(培養液植物)은 유기산총량(有機酸總量)이 무기음(無機陰)이온 총량(總量)보다 초과(超過)되어 유기산(有機酸)에 의한 이온균형(均衡)비율이 크나 $NH_4-N$ 배양액식물은 이온균형(均衡)에 차지하는 유기산(有機酸)비율이 극히 소량이었다. 3. $NO_3-N$식물(植物)은 질산환원(窒酸還元)이 왕성하게 진행되므로서 유리(遊離)된 양(陽)이온과의 이온균형(均衡)을 위하여 유기산(有機酸)이 다량(多量) 함유(含有)되었다.

• 한국환경복원기술학회지
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• 제21권4호
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• pp.1-10
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• 2018

Use of de-icing salts results in accumulation of high concentrations of ions on roadside soils and tree. The purpose of this study isto determine translocation of seasonal impact of exchangeable cations originating from de-icing salt on roadside surface soil-plant influenced by the intensity of foliar damage (NY = 0-25%, SY = 26-50%, CY = 51-75%) of trees. This paper investigated the concentration of four exchangeable cations ($K^+$, $Ca^{2+}$, $Na^+$, and $Mg^{2+}$) on the roadside surface soil. The tree (Ginko biloba) samples were collected from the Konkuk and Judeok intersections in Chung-ju city. The sequential extraction procedure was applied to 120 soil samples of the soilsurface and 30 tree samples. Four cation exchange ions were determined by ICP-OES. The content of four exchangeable cations present on roadside soil was found to be the lowest in NY but highest in CY from tree pits in the order of NY < SY < CY. Especially, the results were apparent during spring time compared to other seasons. Soil collected from tree pits had the highest concentration of $Ca^{2+}$ possibly due to a higher volume of traffic on those streetsresulting in splashing of more calcium chloride ($CaCl_2$). The analysis of three exchangeable cations ($K^+$, $Mg^{2+}$, and $Na^+$) in the tree leaves revealed higher levels than roadside surface soil when foliar damage ratio increased in the order of NY < SY < CY in summer. In addition, a strong positive linear relationship was observed between the concentration of exchangeable cations in soil and trees. It is hypothesized that the results of this study can be a valuable baseline for managing de-icing salt on roadside soil and trees, in order to mitigate the salt stress that can damage the roadside soil and trees.

• Journal of Photoscience
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• 제11권2호
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• pp.83-87
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• 2004

A porphyrin compound containing a crown ether moiety (Por-Crown) and its zinc complex (ZnPor-Crown) have been prepared and the effect of the addition of alkali metal on their fluorescence has been investigated. As alkali metal cations were added, the absorption and fluorescence maxima did not change. However, the absorbance and intensity of fluorescence increased dramatically. Among the alkali metal cations tested, addition of K$^{+}$ and Cs$^{+}$ showed strongest enhancement of absorbance and fluorescence intensity of Por-Crown and ZnPor-Crown.own.

• Bulletin of the Korean Chemical Society
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• 제29권3호
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• pp.539-540
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• 2008

• Bulletin of the Korean Chemical Society
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• 제34권11호
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• pp.3249-3252
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• 2013

We have explored the potential energy surface for the isomerization of the aniline (AN) radical cation to the 2-, 3-, and 4-methylpyridine (picoline, MP) radical cations using G3 model calculations. The isomerization may occur through the 1H-azepine (7-aza-cycloheptatriene) radical cation. A quantitative kinetic analysis has been performed using the Rice-Ramsperger-Kassel-Marcus theory, based on the potential energy surface. The result shows that isomerization between $AN^{+\bullet}$ and each $MP^{+\bullet}$ hardly occurs before their dissociations.

• 대한화학회지
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• 제41권8호
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• pp.437-441
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• 1997

The acid strngth of cations, determined with ICP (Ionic Covalent Parameter): ICP=log(P)-1.38x+2.07 where P is the polarizing power and X its electronegativity expresses the competition between the covalent and ionic forces. This concept, together with electronegativity, is used to describe the properties of oxides with various electronic properties (insulators, metals, degenerate semiconductors, superconductors).

• 대한약학회:학술대회논문집
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• 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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• pp.415.1-415.1
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• 2002

Apical to basal transport of organic cations (OCs) such as tributylmethylammonium (TBuMA), triethyimethylammonium (TEMA). 1-methyl-4-phenylpyridinium (MPP), and berberine across Caco-2 cell monolayers was measured to elucidate the intestinal absorption of OCs. Basal to apical transport of MPP and berberine was larger than apical to basal transport and showed temperature dependency and concentration dependency. indicating that MPP and berberine are secreted into the inteslinal lumen. (omitted)