• Bulletin of the Korean Chemical Society
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• v.3 no.4
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• pp.144-148
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• 1982

The kinetic study on the bromine-exchange reaction of antimony tribromide with t-butyl bromide in nitrobenzene or 1,2,4-trichlorobenzene has been carried out, using Br-82 labelled antimony tribromide. The results show that the exchange reaction is first order with respect to t-butyl bromide and 1.5th order with respect to antimony tribromide. It is assumed that the 1.5th order indicates the coexistance of first- and second-order kinetics. Reaction mechanisms for the exchange reaction are proposed.

• Journal of the Korean Chemical Society
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• v.60 no.6
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• pp.399-401
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• 2016

• Bulletin of the Korean Chemical Society
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• v.28 no.10
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• pp.1643-1644
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• 2007

• Bulletin of the Korean Chemical Society
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• v.23 no.12
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• pp.1819-1822
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• 2002

• Bulletin of the Korean Chemical Society
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• v.28 no.5
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• pp.721-722
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• 2007

• Bulletin of the Korean Chemical Society
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• v.13 no.2
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• pp.184-187
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• 1992

Regeneration methods of oximes, hydrazones, and N,N-dimethylhydrazones to the related carbonyl compounds were effected using various dicarbonyl compounds which are activated with electron withdrawing substituents such as trifluoromethylated $\beta-diketones$, $\beta-acylpyruvates$, and $\alpha-diketones$ via an equilibrium exchange reaction. The chemical transformations of the dicarbonyl compounds in the exchange reaction were investigated by various spectroscopic methods.

• Membrane Journal
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• v.28 no.5
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• pp.326-331
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• 2018

Crosslinking of poly(2,6-dimethyl-1,4-phenylene oxide) (PPO) anion exchange membranes, which can be used for capacitive deionization (CDI), was investigated. PPO Anion exchange polymer was prepared through bromination and amination reaction steps and crosslinked with bisphenol A diglycidylether (BADGE), m-phenylenediamine (m-PDA), and hexamethylenediamine (HMDA). The gelation time by crosslinking was short in the order of HMDA > m-PDA > BADGE. The anion exchange membranes crosslinked at room temperature over a certain amount of crosslinking agent did not dissolve in an aprotic solvent such as 1-methylpyrrolidone (NMP) and the chemical durability of their membranes to organic solvent increased. The ion exchange capacity and water uptake of anion exchange membranes crosslinked with different crosslinker (BADGE) contents were measured and compared. The CDI performance of the crosslinked PPO anion exchange membrane immersed in the HMDA solution was almost the same as that of the non - crosslinked membrane except for the initial stage of the adsorption step.

• Bulletin of the Korean Chemical Society
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• v.25 no.5
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• pp.609-616
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• 2004

Complexation of cesium ion by p-tert-butylcalix[6]arene ethyl ester was studied by NMR spectroscopy in nonpolar $CDCl_3$ and polar acetone-$d_6$ and the results were compared with each other. Analysis of temperature dependent $^1H$ spectra and titration curves reveals that both solvents result in a 1 : 1 cone-form complex with nonpolar $CDCl_3$yielding a more tightly bound one than acetone-$d_6$. Unexpectedly, at very low temperature, we have found that two phenyl ring proton peaks of equal intensity appear both in $CDCl_3$and in acetone-$d_6$ solution which gradually collapse and eventually coalesce into a single line as temperature is raised. This observation could be interpreted in terms of the chemical exchange through direct and/or indirect interconversion between two equivalent conformations possible the complex in both solvents over the temperature range observed. And broadening of $^{133}Cs$ (I = 7/2) nmr line with increasing temperature has also been observed, indicating the exchange of $^{133}Cs$ ion between the complex and the solvent. From numerical fitting of lineshape changes for one-dimensional $^1H$ and $^{133}Cs$ spectra, the exchange rate constants and other relevant parameters for this conformational interconversion and the complex-solvent exchange were deduced.

• KSBB Journal
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• v.24 no.5
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• pp.415-419
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• 2009

In this study, the detoxification methods were evaluated for the removal of fermentation inhibitors from synthetic solution containing the composition similar to the lignocellulosic hydrolysate. The enzyme peroxidase and laccase were used as a biological treatment method. The physico-chemical methods such as adsorption and ion exchange were applied by using activated charcoal and ion exchange resins. The enzyme peroxidase showed a excellent removal of phenolic compounds. The 5-HMF and furfural were completely removed by activated charcoal. The anion exchange resin showed a good result for detoxification of acetic acid. The activated charcoal and ion exchange resins lead to a loss of sugars more or less. The choice of detoxification method must be made after considering the composition and inhibitors in hydrolysates.

• Journal of the Korean Ceramic Society
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• v.33 no.2
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• pp.242-250
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• 1996

Glasses of Na2O-Al2O3-SiO2 system were prepared and ion-exchange characteristics change of properties and bactericidal effects by Na+↔Ag+ ion exchange were studied. Parent glasses with three compositions of varying Na2O in the 20~30 wt% were ion-exchanged in the molten salt of 2 mol% AgNO3+98 mol% NaNO3 at 320~36$0^{\circ}C$ for 15~16min. Amount of ion exchange and penetration depth of Ag+ ion increased with Na2O content in the parent glass ion exchange temperature and time. After ion exchange densities and Vickers hardness of the glasses increased and the glasses showed yellow-brown color and as amount of ion exchange increased the color turned deep because partial reduction and agglomeration of Ag+ into Ag0 results in absorption of visible light. After ion exchange chemical durability of the glass to wter was enhanced compara-bly that weight loss and change of surface of the glass were not found for the leaching test in 5$0^{\circ}C$ K.I water for 240hrs. Bactericidal effect of ion exchanged glass on Staphylococcus aureus and E. coli was determined by microorganism test and bactericidal effect increased with amount of ion exchange and incubation time.