• Journal of Korea Soil Environment Society
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• v.3 no.2
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• pp.71-78
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• 1998

Pyrene is a common petroleum contaminant. This compound is recalcitrant to biological degradation and persists long in contaminated environments. A microcosm experiment was conducted to investigate the degradation rate of pyrene in three different of soil : rhizosphere soil ; non-rhizosphere soil ; and sterilized soil. The degradation rate followed the order of rhizosphere soil)non-rhizosphere soil)sterilized soil. And the rate did not change significantly when organic acids commonly found in the rhizosphere were added to each soil but it seemed to be well related to the increase of the number of microorganisms. Overall, it appears that pyrene is degraded faster in the rhizosphere soil which has the higher microorganism density.

• Journal of Industrial Technology
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• v.32 no.A
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• pp.95-102
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• 2012

To advance luminance efficiency of Titania at visible range, N-doped $TiO_2$ was prepared by using ammonium hydroxide as a source of nitrogen. The photoactivities of the synthesized $TiO_2$ were evaluated on the basis of degradation of humic acid in aqueous solutions with different light sources, UV-C, UV-A and fluorescent lamp. As a result, at UV-C is high efficiency $UV_{254}$ decrease and TOC removal. In this study, the best synthetic conditions of N-doped $TiO_2$ were 5.0 M of ammonium hydroxide concentration and calcination temperature of $550^{\circ}C$. The degradation rate of humic acid as an evaluation of photoactivities of the catalysts were conducted with pH variation, decrease rate of molecular absorption, removal rate of total organic carbon and fluorescece evolution for humic acid solution. XRD and SEM were applied for analysis of surface analysis of the catalysts.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.7 no.6
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• pp.1284-1291
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• 2006

This work examined improving the activity of photocatalyts by novel metal doping for the degradation of volatile organic compounds, such as formaldehyde and acetone. The activity was determined with type of dopant novel metal and volatile organic compounds. The palladium-doped $TiO_2$ was found to be improved the decomposition of acetone. The photocatalytic degradation rate for acetone was increased with decreasing temperature to $45^{\circ}C$. The optmum temperature of photocatalytic degradation rate for formaldehyde was $75^{\circ}C$. The enhancement of reaction rate with novel metal were 1.0 wt.% of palladium for acetone, 1.0 wt.% of plaitnum for formaldehyde.

• Applied Chemistry for Engineering
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• v.32 no.5
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• pp.581-588
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• 2021

In this study, soil slurry bioreactors were used to treat soils containing 16 polycyclic aromatic hydrocarbons (PAHs) for 35 days. Five different soil samples were taken from manufactured gas plant (MGP) and coal tar disposal sites. Soil properties, such as carbon content and particle distribution, were measured. These properties were significantly correlated with percent biodegradation and degradation rate. The cumulative amount of PAH degraded (P), degradation rate (K_m), and lag phase (𝜆) constants of PAHs in different MGP soils for 16 PAHs were successfully obtained from nonlinear regression analysis using the Gompertz equation, but only those of naphthalene, anthracene, acenaphthene, fluoranthene, chrysene, benzo[k]fluoranthene, benzo(a)pyrene, and benzo(g,h,i)perylene are presented in this study. A comparison between total non-carcinogenic and carcinogenic PAHs indicated higher maximum amounts of PAH degraded in the former than that in the latter owing to lower partition coefficients and higher water solubilities (S). The degradation rates of total non-carcinogenic compounds for all soils were more than four times higher than those of total carcinogenic compounds. Carcinogenic PAHs have the highest partitioning coefficients (K_oc), resulting in lower bioavailability as the molecular weight (MW) increases. Good linear relationships of K_m, 𝜆, and P with the octanol-water partitioning coefficient (K_ow), MW, and S were used to estimate PAH remaining, lag time, and biodegradation rate for other PAHs.

• Korean Chemical Engineering Research
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• v.52 no.6
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• pp.695-700
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• 2014

Proton Exchange Membrane Fuel Cells (PEMFC) can generate hydrogen and oxygen from water by electrolysis. But the electrode and polymer electrolyte membrane degrade rapidly during PEM water electrolysis because of high operation voltage over 1.7V. In order to reduce the rate of anode electrode degradation, unsupported $IrO_2$ catalyst was used generally. In this study, Pt/C catalyst for PEMFC was used as a water electrolysis catalyst, and then the degradation of catalyst and membrane were analysed. After water electrolysis reaction in the voltage range from 1.8V to 2.0V, I-V curves, impedance spectra, cyclic voltammograms and linear sweep voltammetry (LSV) were measured at PEMFC operation condition. The degradation rate of electrode and membrane increased as the voltage of water electrolysis increased. The hydrogen yield was 88 % during water electrolysis for 1 min at 2.0V, the performance at 0.6V decreased to 49% due to degradation of membrane and electrode assembly.

• Transactions of the Korean Society of Mechanical Engineers
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• v.16 no.10
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• pp.1908-1914
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• 1992

A significant drag reduction in the turbulent flow of CWM(coal Water Mixture) adding minute amounts of high molecular weight polymer additives has been obtained and it was compared with pure CWM.However, the rate of drag reduction could come down with flow time, which is caused by polymer degradation, The rate of drag reduction and polymer degradation is affected by polymer type, concentration, molecular weight, and flow velocity. In the present investigation, these important parameters were evaluated for their influences on polymer degradation in order to find out stable conditions for CWM transportation with time. It was necessary to determine the more effective type of polymer additives to guarantee the optimum conditions for CWM transport. Experiments were undertaken with a test section of pipe diameter 9.8mm and pipe length 3500mm(L/D=357) in a closed loop, and polyacrylamide and polyetylene oxide were utilized as polymer additives. The tests were carried out under the conditions of 200, 400, 700ppm of polymer concentrations. CWM concentrations utilized were 5% and 10% with flow velocities of 4.9m/s and 6.1m/s. Experimental data show that polyehylene oxide degraded faster than polyacrylamide in CWM transport, and polyacryamide is considered to be a more effective candidate as additive for long time-CWM transport. Polymer degradation is also found to be more likely at lower polymer concentrations, at higher flow velocities, and higher CWM concentrations.

• Korean Journal of Environmental Agriculture
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• v.9 no.1
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• pp.1-8
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• 1990

The effects of soil environmental conditions on the degradation rates of fenitrothion(O-O-dimethyl O-4-nitro-m-tolyl phosphorothioate) in soils under flooded conditions were examined in the laboratory. Fenitrothion was degraded rapidly and the half life period was within 4 days. Furthermore the degradation was mere rapid under flooded conditions than under upland conditions. The decomposition rate was varied with soils and soil temperatures. Fenitrothion degraded more slowly at 30ppm than at l0ppm. Repeated applications of fenitrothion in soils accelerated the degradation rates. The degradation remarkably increased with amendment of rice straw. However, degradation rates ,were virtually unaffected by the addition of the mixed-fertilizer, the fungicide IBP and the herbicide butachlor. The population of fenitrothion-degrading microbes, which were counted by MPN method, always corresponded with the degradation rates in the soils.

• Environmental Engineering Research
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• v.25 no.4
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• pp.571-578
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• 2020

In this work, a detailed study on the electrochemical degradation of an azo dye, Orange G is performed using a platinum electrode. Indeed, the influence of the dye concentration (50-150 mg/L), the pH of the medium and the density of the electric current is studied on the rate of discoloration, the rate of mineralization, the efficiency of the electric current and the energy consumption. The UV-visible spectra of OG plotted against the degradation time show the decrease of the intensity of the characteristic dye peaks. In an environment rich in chlorides, all peaks disappear after 15 min of degradation. However, the peaks at wavelengths of 200 and 290 nm appeared after one hour of treatment. In K₂SO₄, the eliminated percentages are respectively 46, 54 and 61% for wavelengths of 245, 330 and 480 nm. This suggests that the degradation mechanisms in K₂SO₄ and KCl environments are not the same. In the middle rich in chlorides, the eliminated percentage of OG did not seem to be affected by the concentrations increase. These results confirm the hypothesis that electrochemical oxidation process is very favorable for concentrated pollutants discharge.

• The Korean Journal of Food And Nutrition
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• v.20 no.2
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• pp.120-124
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• 2007

The thermal degradation kinetics of alpha-, gamma- and delta-tocopherols was studied during heating at 100, 150 200 and 250$^{\circ}C$ for 5, 15, 30 and 60 min in the absence of oxygen. The tocopherols were separated by HPLC using a reversed phase ${\mu}$-Bondapak C$_{18}$-column with two kinds of elution solvent system in a gradient mode. The kinetics for degradation of ${\alpha}$-, ${\gamma}$- and ${\delta}$-tocopherols was analyzed as a function of temperatures and times. The degradation of tocopherols was described by the first-order kinetics in the absence of oxygen. The rate of tocopherols degradation was dependent on heating temperatures. The degradation rate constants for ${\alpha}$-, ${\gamma}$ and ${\delta}$-tocopherols showed an increasing trend as the heating temperature increased. The magnitude order of the experimental activation energy was ${\delta}$->${\gamma}$->${\alpha}$-tocopherol.

• Journal of Pharmaceutical Investigation
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• v.28 no.2
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• pp.121-126
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• 1998

The solubility and physicochemical stability of caroverine hydrochloride (CRV), an antispasmodic, in buffered aqueous solutions were studied using a reverse phase high performance liquid chromatography. The solubilty of the drug at pH 2.76-5.40 was similar at the range 31.9-36.2 mg/ml $(34^{circ}C)$, but, at the pH higher than 6.0, markedly decreased. The use of polyethylene glycol 400 as a cosolvent did not increase the solubility at any compositions examined. Moreover. increasing molar concentration of aqueous phosphate buffer from 0 to 0.5 M remarkably decreased the solubility. The degradation of CRY followed the apparent first-order kinetics. The degradation was accelerated with decreasing pH and increasing storage temperature. The half-lives for the degradation of CRY (1.0 mg/ml) at pH 1.28. 4.01 and 5.93 $(45^{\circ}C)$ were 2.8, 31.4 and 124 hr. respectively. The pHs of incubated solutions were to some extent lowered perhaps due to the formation of acidic degradation products. The addition of disodium edetate (0.01%) to the CRY solution (pH 4.95) retarded 2.5 times the degradation rate at $45^{\circ}C$, but the use of sodium bisulfite (0.1%) accelerated 2.9 times the rate. The activation energy for the CRY solution (20 mg/ml. pH 5.4) containing 0.01% EDTA was calculated to be 5.98 kcal/mole. When the solution was stored under nitrogen displacement in ampoule, there was no significant degradation even after 3 months at $40^{\circ}C$, indicating that protection from oxidation by air (oxygen) is essential for the complete stabilization of CRY solution.