• Korean Journal of Soil Science and Fertilizer
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• v.44 no.1
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• pp.48-52
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• 2011

The effect of soil water content on the transformation potential of N compounds derived from hydrolysis of urea applied in a reclaimed tidal soils which was saline-sodic was observed to evaluate nitrification rates of urea. Soil samples were collected from Moonpo series at the newly reclaimed area in Saemanguem. For the transformation potential of N compounds from urea (46% N), newly reclaimed tidal soils (RS) were amended with urea at the rates of 0, 10, and 20 kg $10a^{-1}$. With leachate obtained from the incubated RS in a leaching tube at $25^{\circ}C$, urea hydrolysis and nitrification were measured for a total of 30days. The cumulative amounts of $NO_3{^-}$-N in each of the four soils treated with urea was linear with time of incubation. Results showed that increase in pH occurred with increasing application rate of urea and volumetric water content due to hydrolysis of urea. The total N in the RS was decreased with incubation time, indicating that rates of urea hydrolysis was influenced by soil moisture conditions. Also, the cumulative amount of nitrate in RS gradually increased with increase in time of incubation.

• Journal of Applied Biological Chemistry
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• v.43 no.2
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• pp.86-93
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• 2000

An experiment was conducted to obtain the quantitative data on the transformation and loss of applied urea-N in waterlogged soil columns. The soil columns were pre-incubated for 35 days to develop oxidized and reduced soil conditions prior to urea application. After urea application at the rate of $150kg\;N\;ha^{-1}$(29.5 mg N), the amounts of nitrogen which were volatilized, leached, and remained in soil column were measured during 38 days of incubation period. On 2 and 4 days of incubation, 54.1%(15.9 mg N) and 98.4%(29.0mg N) of the applied urea was hydrolyzed, respectively. Most of the applied urea was completely hydrolyzed within 6 days. After urea application, the rates of ammonia volatilization were increased with the floodwater pH when the floodwater pH were higher than 7.0. The maximum rate of ammonia volatilization was $0.3mg\;d^{-1}$ when pH of the floodwater showed maximum value of 7.6. The total amount of volatilized nitrogen was 6.1% (1.8mg N) of the applied urea-N. A 63.2 % (18.6mg N) of the applied urea was remained in soil as $NH_4{^+}-N$ and 28.0% (8.2mg N) of the applied urea was leached as $NH_4{^+}-N$ at the end of the incubation. Amount of $NO_3{^-}-N$ in soil was smaller than 2.0 mg throughout the incubation period. The total amount of $NO_3{^-}-N$ leached was very small, which value was 1.8 mg. It suggested that nitrification process was not significant in waterlogged soil column of this study due to high infiltration rate of urea solution applied to the soil column. Therefore only small amount of $NO_3{^-}-N$ was lost by denitrification and leaching process.

• Korean Journal of Soil Science and Fertilizer
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• v.44 no.1
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• pp.84-90
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• 2011

It is imperative to study the hydrolysis of urea in high saline-sodic condition of a newly reclaimed tidal land in order to overcome the problems associated with use of urea fertilizer. The methodology adopted in this study tried to get a convenient way of estimating rate for N transformation needed in N fate and transport studies by reviewing pH and salt contents which can affect the microbial activity which is closely related to the rate of urea hydrolysis. The hydrolysis of urea over time follows first-order kinetics and soil urease activity in reclaimed soils will be represented by Michaelis-Menten-type kinetics. However, high pH and less microorganisms may delay the hydrolysis of urea due to decrease in urease activity with increasing pH. Therefore, the rate of urea hydrolysis should adopt $V_{max}$ referring enzyme activity ($E_0$) accounting for urease concentration which is indicative for urea hydrolysis, especially in a high saline and sodic soils.

• Korean Journal of Soil Science and Fertilizer
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• v.21 no.1
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• pp.73-78
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• 1988

A laboratory experiments were carried out to study the urea transformation and kinetics of soil urease in paddy soils with different properties. Urea transformation in paddy soils followed first-order kinetics, the rate of urea hydrolysis and the first-order constant was higher in the soil with high total urease activity (TUA) and accumulated urease activity (AUA) than those with low TUA and AUA. The values of Km and Vmax indicated that the Km values of accumulated urease in the soils were different in each soils and lower than that of microbial urease. However, the Km values of microbial urease were nearly same each other.

• Korean Journal of Soil Science and Fertilizer
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• v.44 no.5
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• pp.745-751
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• 2011

In most agricultural soils, ammonium ($NH_4^+$) from fertilizer is quickly converted to nitrate ($NO_3^-$) by the process of nitrification which is crucial to the efficiency of N fertilizers and their impact on the environment. However, nitrification studies have been studied extensively in agricultural soils, not in a newly reclaimed tidal soil which show saline-sodic and high pH. Therefore, understanding the fate of nitrogen species transformed from urea introduced into reclaimed tidal soil is important for nutrient management and environmental quality. This paper reviewed studies regarding to transformation and fate of nitrogen sources such as urea under the circumstances of a reclaimed tidal soils located in a western coastal area.

• Journal of Photoscience
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• v.6 no.4
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• pp.177-181
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• 1999

The photochemical transformation of carbon monoxide in aqueous ammonia solution has been investigated at 25${\pm}$0.1$^{\circ}C$ using 184.9 nm UV light. Amination and carbonylation processes were carried out by irradiating the aqueous ammonia solution saturated with carbon monoxide, and the formation of formamide, urea, hexamethylenetetramine, formaldehyde, glyoxal and hydrazine was observed. The formation of hydrazine was affected by the presence of ammonia, and the formation of carbonyl compounds such as formaldehyde and glyoxal was influenced by the presence of carbon monoxide. The formation of formamide, urea and hexamethylenetetramine was affected by both ammonia and carbon monoxide. The initial quantum yields of the products were determined and probable mechanisms for the photochemical reaction were presented on the basis of product analysis.

• Applied Biological Chemistry
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• v.20 no.1
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• pp.58-65
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• 1977

A laboratory experiment was carried out with loamy paddy soily under Hooded condition to study the effects of some pesticides on the decomposition rate of urea and the transformation of nitrogen. The pesticides used in this study are ten kinds, which are usually applicable for rice cropping. The soil was treated with 200ppm of fertilizer urea-N and different levels of pesticides and then incubated at $28{\pm}1^{\circ}C$ for two weeks. The kinds of pesticides used in this study were three kinds of herbicides (2,4-D, Machete and TOK), three kinds of fungicides (Rabcide, Neo-asozine and Phenazine) at the levels of 20,100 and 200ppm and four kinds of insecticides (Birlane, Diazinon, Sumithion and Bux) at the levels of 50,250 and 500ppm. respectively. The results obtained may be summarized as follows. 1. The treatments of herbicides and fungicides show little effect on the decomposition rate of urea at the levels of 20 and 100ppm, but by the treatment of 200ppm it was retarded markedly after one day incubation aside from Rabcide and Neo-asozine. The decomposing rate of urea was inhibited weakly by the treatment with 250ppm of Sumithion and Bux, however, 500ppm of all kinds of insecticides treated in this study brought about strong inhibitory effect (over 50%) after only one day incubation. The applied urea was disappeared nearly completely in three days in all cases with and without pesticides. 2. The production of ammonium-N was increased with the increase of pesticide concentrations gradually through two weeks and otherwise in the control sample a loss of inorganic-N resulted in about 20% extent. 3. The inhibitory effect of the all applied pesticides on_the_ nitrification under flooded condition was observed markedly and may be ordered as insecticides, herbicides and fungicides according to its inhibiting action.

• Elastomers and Composites
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• v.50 no.2
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• pp.92-97
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• 2015

A study on reaction kinetics for a PTMG/TDI prepolymer with 2,2'-dichloro-4,4'-methylenedianiline (MOCA), of which formulations may be generally used for fabricating high performance polyurethane elastomers, was peformed using non-isothermal differential scanning calorimetry (DSC). A number of thermograms were obtained at several constant heating rates, and analysed using Flynn-Wall-Ozawa (FWO) isoconversional method for activation energy, $E_a$ and extended-Avrami equation for reaction order, n. Urea formation reaction of the present system was observed to occur through the simple exothermic reaction process in the temperature range of $100{\sim}130^{\circ}C$ for the heating rate of $3{\sim}7^{\circ}C/min$. and could be well-fitted with generalized sigmoid function. Though activation energy was nearly constant as $53.0{\pm}0.5kJ/mol$, it tended to increase a little at initial stage, but it decreases at later stage by the transformation into diffusion-controlled reaction due to the increased viscosity. Reaction order was evaluated as about 2.8, which was somewhat higher than the generally well-known $2^{nd}$ order values for the various urea reactions. Both the reaction order and reaction rate explicitly increased with temperature, which was considered as the indication of occurring the side reactions such as allophanate or biuret formation.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.14 no.6
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• pp.267-271
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• 2004

Lithium cobalt oxide $(LiCoO_2)$ cathode powders for rechargeable battery have been successfully prepared using urea hydrolysis method. The obtained hydrolysis-derived precursors with different Li/Co molar ratio were calcined at various temperatures. Low temperature phase $(LT-LiCoO_2)$ and high temperature phase $(HT-LiCoO_2)$ were obtained after calcination at $500^{\circ}C$ for 2 hr, and phase transformation from $LT-LiCoO_2{\;}to{\;}HT-LiCoO_2$ was completely occurred over $700^{\circ}C$. The layered structure of $LiCoO_2$ was well developed with a rise in the calcination temperature. Charge-discharge test show that the lithium cobalt oxide with 1.2 molar ratio prepared at $800^{\circ}C$ has an initial discharge capacity as high as 152 mAh/g, and the relatively stable cycling characteristic with 9.2 % of capacity fading was obtained after 40th charge-discharge test.

• The Korean Journal of Pesticide Science
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• v.8 no.1
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• pp.38-45
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• 2004

To elucidate the photolysis characteristics of the insecticide imidacloprid in the environment, $[^{14}C]$imidacloprid was treated into water and paddy soil-water system. In water system, the amount of $^{14}C$-radioactivity distributed in aqueous phase was rapidly increased up to 80% of total $^{14}C$ in water during 7 days of exposure to sunlight. Also, the amounts of imidacloprid in water at day 0 and 3 days after treatment were 1.2461 and 0.8594 mg/kg, respectively, not being detected 7 days after treatment, indicating rapid degradation of imidacloprid in water by sunlight. One photodegradation product, imidacloprid urea, in which the $N-NO_2$ moiety of imidacloprid was replaced by oxygen, was detected from water in water and water-paddy systems. The amount of the metabolite detected from water in water system was 0.0112 mg/kg 1 day after treatment and reached the top concentration of 0.0391 mg/kg 7 days after treatment. In case of water-paddy system, its amount was 0.0117 mg/kg 1 day after treatment and reached the highest concentration of 0.0259 mg/kg 3 days after treatment. Rapid transformation of imidacloprid into polar compounds continued until 7 days after treatment, considering that 80% of $^{14}C$ in water distributed in aqueous phase 7 days after treatment, amount of imidacloprid was 1.6538 mg/kg at day 0 and 0.8785 mg/kg 1 day after treatment, not being detected after 15 days, indicating rapid degradation of imidacloprid in water-paddy soil system by sunlight. The direct degradation of imidacloprid to imidacloprid urea would be a major photodegradation pathway in water and water-paddy soil systems.