• Resources Recycling
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• v.17 no.6
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• pp.34-42
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• 2008

The properties of sodium silicate solution were surveyed by using the yellow silicomolybdic method, and the formation of silica sol from sodium silicate solution and the growth of silica sol were investigated in this study. The $SiO_2$ content of 2 wt% in sodium silicate solution was proper to oxidize sodium silicate with sulfuric acid. After the removal of sodium ions in sodium silicate solution, the pH of silicate solution had to be controlled above 9 for the stabilization of silicate solution. The condensation between silicic acid species and silica nuclei surfaces has been studied at $20{\sim}80^{\circ}C$ and pH 10 in silicate solutions with silica nuclei. The reaction falls into two kinetics regimes, limited at high silicic acid species concentration by polymerization, but at lower concentration by a process whereby deposited silicic acid species condenses further to silica. The overall condensation is first-order in silicic acid species concentration, proceeded toward to pseudo equilibrium concentration, $C_x$, rather than the solubility of amorphous silica. The heat of solution of amorphous silica was 3.34 kcal/mol and exhibits an Arrhenius temperature dependence with an apparent activation energy of 3.16 kcal/mol in the range of $20{\sim}80^{\circ}C$.

• Journal of the Korean Chemical Society
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• v.39 no.8
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• pp.604-610
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• 1995

The interaction between 3,3'-dipropyl oxacarbocyanine and poly(styrenesulfonate) has been studied by means of absorption and fluorescence spectroscopic methods. The results was interpreted by stacking model. The kinetic studies of the interaction between 3,3'-dipropyl oxacarbocyanine and poly(styrenesulfonate) were carried out by the absorption and fluorescence spectroscopic stopped-flow methods. The observed relaxation effect in DPC-PSS system was described quantitatively by assuming two relaxation processes. The dependence of rate of reaction on the salt concentration of the solution was also studied. The results are consistent with the two-step mechanism.

• Journal of the Korean Chemical Society
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• v.54 no.5
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• pp.603-610
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• 2010

The potential feasibility of Maghnia clay as adsorbent to remove three cationic dyes (methylene blue (MB), neutral red (NR) and malachite green oxalates (MG)) from aqueous solution was investigated at various operating parameters such as contact time, pH, initial dye concentration and adsorbent dose. Optimum pH values for dyes adsorption were 6 for NR and 7 for MB and MG, respectively. Maximum adsorption of dyes, i.e. $\geq$ 90% has been achieved in aqueous solutions in 60 minutes. The adsorption of dyes followed the pseudo-second-order rate equation.

• Journal of the Korean Chemical Society
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• v.36 no.6
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• pp.919-924
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• 1992

The kinetics of the hydrolysis of N-benzylidenebenzenesulfonamide derivatives have been investigated by ultraviolet spectrophotometry in $H_2O$ at $25^{\circ}C$. A rate equation which can be applied over a wide pH range was obtained. The substituent effect on the hydrolysis of N-benzylidenebenzenesulfonamide derivatives were studied and rate of hydrolysis is known to be accelerated by electron withdrowing group. Final product of the hydrolysis was benzenesulfonamide and benzaldehyde. Base on the rate equation, substituent effect, general base effect and final products, hydrolysis of N-benzylidenebenzenesulfonamide derivatives seemed to be initiated by the hydronium ion at the pH 0.2${\sim}$2.5 and proceeded by the neutral $H_2O$ molecule at pH 3.0${\sim}$8.0 but proceeded by the hydroxide ion at above pH 8.5.

• KSBB Journal
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• v.6 no.1
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• pp.99-103
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• 1991

The optimum conditions and rates of absorption of isobutylene in aqueous para-toluene sulfonic acid(PTSA) were studied experimentally in a stirred reactor. The effects of acid concentration(30-70 wt%), acid loading (0.3-5), mixing intensity(400-1000 rpm), and temperature ($20-80^{\circ}C$) on the absorption conditions were examined. The absorption rate of isobutylene was first order in isobutylene and variable order in PTSA concentrations. The apparent energy of activation was found to be 13 Kcal/mole.

• Korean Chemical Engineering Research
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• v.46 no.3
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• pp.535-539
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• 2008

Conversion to oil, yield of styrene and formation of side products such as ${\alpha}-methyl$ styrene, ethyl benzene, benzene, toluene, dimer and trimer were affected by residue formed during thermal degradation. Also, control of reaction temperature had a difficulty at the first stage. Thus, new reaction system using wetted-wall type reactor was proposed and examined on various parameters such as reaction temperature, feeding rate and removal velocity of formed vapor. Optimun condition was obtained from continuous thermal degradation using wetted-wall type reactor and reaction kinetic study was carried out at new type reactor.

• Applied Chemistry for Engineering
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• v.19 no.2
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• pp.191-198
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• 2008

The thermal degradation characteristics of high molecular components obtained from pyrolysis of mixed waste plastics have been studied by thermogravimetric analysis (TGA) and gas chromatography spectrometry (GC-MS). The kinetics of thermal degradation has been studied by a conventional nonisothermal thermogravimetric technique at several heating rates between 10 and $50^{\circ}C/min$. The dynamic thermogravimetric analysis curve and its derivative have been analyzed using a variety of analytical methods reported in the literature to obtain information on the kinetic parameters such as activation energies and reaction orders. The yields of liquid products have been monitored by batch pyrolysis reactor under various reaction temperatures and reaction times. And the characteristic of liquid products with the increase in reaction temperature has been performed by GC-MS.

• Journal of the Korean Chemical Society
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• v.13 no.4
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• pp.263-272
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• 1969

액체의 상태합을 유도하여 여러 가지 액체들의 적용하여 열역학적 성질들과 점성도를 계산하여여 측정치와의 좋은 일치를 보았다. 그리고 이 상태합을 써서 여러 성분으로 된 액체 용액의 상태합을 얻었으며 나아가서 액체 용액에서의 화학 반응 속도를 구할 수 있음을 보았다.

• Korean Chemical Engineering Research
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• v.47 no.3
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• pp.380-385
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• 2009

The absorption rate of carbon dioxide with 2-amino-2-methyl-1-propanol(AMP) was measured in such non-aqueous solvents as methanol, ethanol, n-propanol, n-butanol, ethylene glycol, propylene glycol, and propylene carbonate, and in water at 298 K and 101.3 kPa using a semi-batch stirred tank with a plane gas-liquid interface. The overall reaction rate constant, obtained under the condition of fast reaction regime, from the measured rate of absorption was used to get the elementary reaction rate constants in complicated reactions represented by reaction mechanism of carbamate formation and the order of overall reaction of $CO_2$ with amine. The correlation between the elementary reaction rate constant and the solubility parameter of the solvent was also presented.

• Journal of the Korean Chemical Society
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• v.17 no.2
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• pp.130-135
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• 1973

The rate-constants of hydrolysis of 3, 4-methylenedioxyphenylmethylenemalononitrile are determined by ultraviolet spectrophotometry at various pH and a rate equation which can be applied over wide pH range is obtained. The rate equation reveals that below pH 5.0 and above pH 9.0, the hydrolysis is initiated by the addition of water and hydroxide ion respectively. However, at pH 6.0-8.0 the competitive addition of water and hydroxide ion occurs. The catalytic contribution of hydroxide ion and water can be fully explained by the rate equation obtained.