• Korean Journal of Weed Science
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• v.18 no.4
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• pp.325-332
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• 1998

This study was carried out to investigate the adsorption and the movement of herbicide fenoxaprop-P-ethyl in the silty clay soil(SiC) and the sandy loam soil(SL). Fifteen percent of the added herbicide was adsorbed within 30 min after shaking, and a quasi-equilibrium was reached after 8 to 14 h. The time required for 50% adsorption was 15.8 h in the SiC and 19.3 h in the SL. The equilibrium adsorption isotherm was followed by the Freundlich equation and the Kd was 3.86 in the SiC and 2.32 in the SL. The herbicide in the soil columns flooded with 3 cm water depth and eluted at 0.8 cm/day was leached to 6 cm and 8 cm depth at 7 and 21 days after the treatment, respectively. However, the movement was widened with increased amount of leaching water. The herbicide in the field soils was moved up to 6 cm and 8 cm depth at 14 and 56 days after the treatment, respectively. However, the large amount of the applied herbicide was distributed in 0~2 cm profile in all of the soils examined. Half-life of the chemical in soils was shorter than 7 days and the time to 90% degradation was about 4 weeks. The results indicate that the herbicide has relatively small mobility and short persistence.

• Journal of the Korean Geotechnical Society
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• v.24 no.9
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• pp.13-21
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• 2008

Partitioning tracer method is a useful tool to characterize large domains of the aquifers contaminated with light nonaqueous phase liquids (LNAPLs). Sorption of the partitioning tracers to the organic matter content of soil can potentially influence the efficacy of partitioning tracer method. LNAPL-water partitioning coefficients of tracers ($K_{nw}$), measured by static method, showed linear relationship. Sorption isotherm tests were conducted to evaluate the sorption capacity of the soils packed in the columns and the results were appropriately represented by Freundlich sorption isotherm. The sorption of tracers proportionally increased with the increase of the organic matter content of the soil. Laboratory experiments were conducted in four columns each packed with soils of different organic matter contents to determine the potential interference effects of sorption to soil organic matter content and correction factors for the errors in estimation of LNAPLs by partitioning tracer method. Though there were no contaminants added, breakthrough curves from columns packed with mixture of Jumunjin standard sand and organic matter showed separation of tracers. Columns were then contaminated to residual saturation with kerosene and breakthrough curves were obtained. The results show that sorption of tracers to soil organic matter leads to an increase in the retardation factor (R) and hence, to an overestimation of the saturation of LNAPLs. A relation between the percentage of organic matter content and the corresponding percentage error in the estimation of NAPLs has been developed.

• Korean Journal of Soil Science and Fertilizer
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• v.45 no.2
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• pp.204-208
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• 2012

Water repellency which affects infiltration, evaporation, erosion and other water transfer mechanisms through soil has been observed under several natural conditions. Water repellency is thought to be caused by hydrophobic organic compounds, which are present as coatings on soil particles or as an interstitial matter between soil particles. This study was conducted to evaluate the characteristics of the water repellent soil and transport characteristics of trace elements within this soil. Capillary height of the water repellent soil was measured. Batch and column studies were accompanied to identify sorption and transport mechanism of trace elements such as $Cu^{2+}$, $Mn^{2+}$, $Fe^{2+}$, $Zn^{2+}$ and $Mo^{5+}$. Difference of sorption capacity between common and repellent soils was observed depended on the degree of repellency. In the column study, the desorption of trace elements and the spatial concentration distribution as a function of time were evaluated. The capillary height was in the repellency order of 0% > 15% > 40% > 70% > 100%. No water was absorbed in soil indicating >70% repellency. Using trace elements, $Fe^{2+}$ and $Mo^{5+}$ showed higher sorption capacity in the repellent soil than in non-repellent soil. The sorption performance of $Fe^{2+}$ was found to be in the repellency order of 40% > 15% > 0%. Our results found that transfer of $Mo^{5+}$ had similar sorption tendency in soils having 0%, 15% and 40% repellency at the beginning, however, the higher desorption capacity was observed as time passes in the repellent soil compared to in non-repellent soils.

• Economic and Environmental Geology
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• v.31 no.4
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• pp.291-296
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• 1998

Pedogenic hematite is a well known agent for sink of pollutants and nutrients and for aggregation of particles in soils. Changes in physical and chemical properties of two sandy loam soils (Anahuac and Crowley soils) from the Southern Coastal Plain, the United States of America, were tested after adding finely ground crystalline hematite prepared for drilling fluid weighting material. There was an increase in hydraulic conductivity (HC) of the soils with addition of up to 3% by weight of hematite but a decrease in HC with addition of more hematite. The aggregate stability (AS) of the soils was not affected by adding hematite. Anahuac soil with higher content of organic matter and lower sodium adsorption ratio (SAR) had higher values of HC and AS than Crowley soil. Adding hematite also resulted in a slight increase in zinc (Zn) adsorption by the soils, but had no influence on the adsorption of phosphate.

• Korean Journal of Soil Science and Fertilizer
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• v.35 no.6
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• pp.344-351
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• 2002

Chemical speciation and transport of heavy metals in soil environment could be controlled by humic acid. In order to understand the mechanism on competitive adsorption of Cd and Cu on the surface of humic acid extracted from peat, the charge development of humic acid were investigate through a batch adsorption experiment with a series of different background electrolytes levels. The competitive adsorption of Cd and Cu to the humic acid were estimated according to the model using the proton binding constant obtained from the above batch test. The affinity of Cu to the carboxyl group on the humic acid was higher than that of Cd, but the affinity to the phenolic group was lower than to the carboxyl group. It seems that the amount of adsorbed Cd and Cu could be estimated using the proton binding constant obtained from a solution with single background ion. However, it is difficult to interpret the competitive adsorption of Cd and Cu with the constant for single background ion.

• Korean Journal of Weed Science
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• v.18 no.3
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• pp.257-261
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• 1998

This study was carried out to investigate the adsorption and the degradation of herbicide napropamide in soils tinder laboratory conditions. The adsorption distribution coefficients(Kd) of napropamide in 3 soils varied from 5.38 to 11.39. With higher content of organic matter in soils, the extent of adsorption was high. The rapid degradation of napropamide took place after a lag period. The time to 50% loss of napropamide was approximately 65, 45 and 30 days in soil incubated at 10, 20 and $30^{\circ}C$, respectively. The time to the 90% loss varied from about 90 days at $10^{\circ}C$ to about 45 days at $30^{\circ}C$. In the soil pre-incubated with napropamide, the herbicide degraded without a lag time, and the rate of degradation was also accelerated. This should be a evidence on enhanced biodegradation of napropamide in soil with the repeat-application.

• Korean Journal of Soil Science and Fertilizer
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• v.41 no.6
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• pp.369-373
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• 2008

Special concern has been given to the elevated arsenic content in soils because of its high mobility and toxicity. Layered double hydroxide (LDH) which has a high anionic exchange capacity is another potential anion adsorbent for toxic anions such as arsenic, chromate and selenium etc. The uptake of arsenate from aqueous solutions by the calcined Mg-Al LDH has been investigated. The sorption capacity was about 530 mmol/kg. Sorption isotherm was defined as L-type in which arsenate was removed by LDH through anion uptake reaction. Arsenate sorption by the calcined Mg-Al LDH was occurred by reconstruction of LDH's framework. Competitive adsorption revealed that Mg-Al LDH had higher selectivity for arsenate than for sulfate. These results strongly suggest that calcined Mg-Al LDH has a promising potential for efficient removal of toxic metal oxides like arsenates from aqueous environments.

• Journal of Korea Soil Environment Society
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• v.2 no.2
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• pp.61-72
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• 1997

This research aims to remove the heavy metals, nonbiodegradable COD(NBDCOD), and color using the coal waste. The experimental by heat treatment was performed to advance the adsorption capacity. The results are as follows ; i) The coal waste had the adsorption capacity of heavy metals and the rates were in the range of 20 to 30 percents. ii) The heat treatment was the optimum condition that the reaction time was 6 hours at $500^{\circ}C$, , iii) In the column experimen, non-treated coal waste removed the COD and color in the range of 20 to 60 percents. iv) Heat-treated coal waste showed higher removal rate of the color in biological effluent, and heavy metal and COD removal rates were changed by the filteration rates.

• The Journal of Engineering Geology
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• v.17 no.1 s.50
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• pp.143-150
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• 2007

AMD (Acid mine drainage) from disused mines is one or the most significant pollutant problems to make harmful effect to human health. We demonstrated the mechanism of resolution and adsorption reaction for arsenic, manganese and zink from the soil and mine tailings which were located in the vicinity of a disused mine in Kyoungnam area. The resolution experiments were carried with a column test f3r 45 days continuously. Metal chemical forms in water were changed with the condition of solution pH and ORP (oxidation-reduction potential). Metal chemical forms affected on the reaction of resolution and adsorption of metals in water environments. Even though the sampling was carried in very closed location, there was significant different results of pollution level and ORP changes in terms of column operations. Hence It was important to note the pH and ORP in AMD to evaluate a risk assessment and a soil management using monitoring metals. When we operate AMD management with the mechanism of resolution and adsorption it can be achieved better economic solution.

• Journal of Korea Soil Environment Society
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• v.4 no.2
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• pp.33-43
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• 1999

A strain (designated SK3l) which produces an excellent adsorption substance was isolated from soil samples and identified as Bacillus specied. The major adsorption substance (biosorbent SK3l) produced by Bacillus sp. SK31 was purified by ethanol precipitation and cetylpyridinium (CPC) precipitation. The adsorption charactics of zinc and lead ions on bioadsorbent SK3l were investigated. The equilibrium isotherms showed that bioadsorbent SK3l took up zinc and lead from aqueous solutions to the extent of about 52 mg/g and 112 mg/g. respectively. The culture conditions at the flask level of Bacillus sp. SK3l were investigated for the production of polysaccharide bioadsorbent, SK3l. The optimum pH and temperature for sorbent production were 7.5 and $30^{\circ}C$, respectively. The important carbon and nitrogen sources for sorbent formation were glucose and ammonium nitrate, respectively. In the optimized medium, sorbent production was improved three folds in comparison with the basal medium. In the jar fermenter, the highest sorbent production was obtained at 60 h cu1tivation time and the amount of biosorbent SK3l at that time was 9.2 g/$m\ell$.