• Journal of Korea Technical Association of The Pulp and Paper Industry
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• v.36 no.5 s.108
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• pp.78-84
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• 2004

Lignin precipitated from black liquor of soda pulping of bagasse was used to prepare cation-exchange resin. The effect of sulfuric acid treatment, concentration of phenol and formaldehyde on the properties of the prepared cation-exchange resin was investigated. It was found that sulfonated resinified phenolated lignin gave a resin with an ion-exchange capacity higher than that of resin, which resulted from sulfonation of resinified lignin at zero phenol concentration. Infrared spectroscopy of the prepared ion-exchange resin shows anew bands at 1060, 1160, 1280 and $1330\;cm^{-1}$ which indicated to the presence of $SO_{3}$.

• Korean Journal of Microbiology
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• v.9 no.4
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• pp.145-148
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• 1971

Mitochondria were isolated from Chlorella cells effects of cation on solute permeability of mitochondrial membrane were investigated using P$^{32}$ as a tracer. It was strikingly increased uptake of phosphate for NaCl, KCl, while evidently decreased phosphate uptake of mitochondrial membrane for $MgCl_2$, $CaCl_2$. This consider that uptake of monovalent cation were increased, but uptake of divalentcation were decreased for permeability of mitochondrial membrane as if the permeability of protoplasmic membrane.

• Applied Chemistry for Engineering
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• v.5 no.3
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• pp.438-442
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• 1994

A very useful cation radical, triphenylaminium hexachloroantimonate, was quantitatively incorporated into insoluble polymer framework. The polymer cation radical was found to be effective as a catalyst in the Diels-Alder type dimerization and then shown to be reusable through several cycles of use.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.19 no.5
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• pp.237-241
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• 2009

Dislocation dipoles were formed in the early stage of deformation of Y-CSZ single crystal at high temperatures. And the dipoles were pinched off to break into dipoles loops by dislocation climb. Dislocation loop annealing was peformed in Y-CSZ single crystal to evaluate the diffusivity of cation which was the rate-controlling ion.

• Bulletin of the Korean Chemical Society
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• v.34 no.11
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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.

• Journal of the Korean institute of surface engineering
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• v.21 no.3
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• pp.95-102
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• 1988

The anodic oxidation of aniline in aqueous sulfuric acid solution on a platinum was studied. To examine of mechanism of this reaction, the date were obtained during controlled potential electrolysis, aided by computer system. The reaction mechanism was assumed the electrochemical-chemical-electrochemical(ECE) mechanism. We obtained the result that the intial charge transfer step proceeds through a radical cation, and this radical cation were bound cation led to may type of dimer in which p-aminodiphenylamine was de-electronated again to give the polymer.

• Bulletin of the Korean Chemical Society
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• v.5 no.6
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• pp.211-215
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• 1984

Reaction of thianthrene cation radical perchlorate (1) with tert-butyl peroxide (TBP) in acetonitrile gave thianthrene (2), thianthrene 5-oxide (3), cis-thianthrene-5,10-dioxide (4), 5-acetonylthianthrenium perchlorate (9), along with small amount of thianthrene-5,5-dioxide (7) in some cases. Isolation of N-tert-butylacetamide indicated the formation of tert-butyl cation from TBP. The formation mechanisms of these products were proposed.

• Proceedings of the Korean Vacuum Society Conference
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• 2012.08a
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• pp.71-71
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• 2012

Chemically modified graphene has been great interest for the application of printed electronics using solution prossesable technique. Here, we demonstrate a large area graphene exfoliation method with fewer defects on the basal plane by application of shear stress in solution to obtain high quality reduced graphene oxide (RGO). Moreover, we introduce a novel route to preparing highly concentrated and conductive RGO in various solvents by monovalent cation-${\pi}$ interaction. Noncovalent binding forces can be induced between a monopole (cation) and a quadrupole (aromatic ${\pi}$ system). The stability of this RGO dispersion was more sensitive to the strength of the cation-${\pi}$ interactions than to the cation-oxygen functional group interactions. The RGO film prepared without a post-annealing process displayed superior electrical conductivity of 97,500 S/m. Our strategy can facilitate the development of large scalable production methods for preparing printed electronics made from high-quality RGO nanosheets.

• Journal of the Korean Ceramic Society
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• v.41 no.6
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• pp.425-429
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• 2004

[DEACOOH]-Montmorillonite intercalations complex obtained from Na-Montmorillonite and 10-Carboxy-n-decyldimethylethylammonium bromide (organic cation) was reacted with the monomer ($\varepsilon$-caprolactone) to achieve the [DEACOOH]-$\varepsilon$-caprolactone-Montmorillonite intercalations complex. From this intercalations complex Montmorillonite/Polycaprolactone nanocomposites in which montmorillonite (inorganic polymer) is chemically linked with the polycaprolactone (organic polymer) were formed at 240$^{\circ}C$ by three different methods such as in stoichiometric amounts between monomer and organic cation, in excess of only the monomer and in excess of both organic cation and monomer. The products obtained after polymerization were analyzed with X-ray diffractometer and TEM.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2002.04a
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• pp.38-43
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• 2002

A series of tests were performed to investigate the effects of pH and contamination level on cation exchange capacity and zeta potential in kaolinite loaded with lead. Test results show that cation exchange capacity of kaolinite is found to be in the range from 4 to 20meq/100g and it increased with increasing pH up to the converged number about 20meq/100g over pH 8. And then CEC has a tendency to reduce and converge to zero with increasing the concentration of Pb in the kaolinite surface. Moreover, zeta potential of kaolinite contaminated with lead is found to be in the range from -10 to 5mV, and zero point of charge is measured at about pH 3.5. Zeta potential of kaolinite contaminated with lead decreases with increasing pH values and decreasing Pb concentration of kaolinite.