• Journal of Korea Soil Environment Society
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• v.1 no.1
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• pp.81-88
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• 1996

To study the Cd adsorption in the presence of competing ions in soil-solution interphase, three soil samples from the Bt horizon were taken and analyzed for their physical and chemical properties. Adsorption of ethylene glycol monoethyl ether(EGME) and N, were determined to establish the specific surface area of the soils. We attempted to establish a qeneralizing competitive sorption isotherms for soils of entirely different composition of the solid phase, resulting in the routine use as a guidelines for the fate of reactive solute in soil profiles. Many physicochemical factors including competitive adsorption bettween solutes will affect the general adsorption phenomena as shown in a single not only on the soil:solution ratio used, but also on the surface areas of its respective soil samples. This phenomenon was attributed to competition Cd for sorption sites with Mg by different soil constituents. These adsorption isotherms are able to use as examples to demonstrate that this phenomenon can complicate the development of a standardized batch adsorption procedure as well as interpreting fate and adsorption of toxic inorganic compounds.

• Journal of Korea Soil Environment Society
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• v.4 no.1
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• pp.3-11
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• 1999

The effects of major cations in soils, soil : extractant ratio, and EDTA : lead stoichiometric ratio on the extraction efficiency of lead using EDTA were studied for 4 different actual lead-contaminated soils and one artificially lead-contaminated soil. Extraction of lead from the lead-contaminated soil was not affected by a soil : extractant ratio as low as 1 : 3 but instead was dependent on the quantity of EDTA present. Results of the experiments showed that the extraction efficiency for each soil was different, but if sufficiently large amount of EDTA was applied, all the lead may be extracted except for a soil from lead mining area. The differences in extraction efficiencies nay be due to the major cations present in soils which may compete with lead for active sites on EDTA. The total molar amount of major cations extracted was as muck as 20 times more than the added molar amount of EDTA. For some of the soils tested, the extraction efficiency of lead may be affected by being occluded in the Fe and Mn oxides present in the soil. While major cations present in the soil may be one of the factors affecting lead extraction efficiency, the type of lead species present may also play a role. When these factors affect severely, the using of EDTA to extract lead from lead-contaminated soil might be non-effective method.

• Journal of Korean Society of Environmental Engineers
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• v.35 no.12
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• pp.861-866
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• 2013

The aim of this study was to investigate the biodegradation of dissolved organic matter derived from animal carcass disposal soil using soil inhabited bacteria and to identify the bacteria involved in the biodegradation. The two soils were obtained from the animal carcass burial sites located in Anseong, Gyeonggi-do, Korea. The results indicated that during the biodegradation experiments (56 days), 48% of dissolved organic carbon (DOC) was mineralized within 13 days in soil-derived solution 1 (initial DOC = 19.88 mgC/L), and the DOC concentration at 56 days was $8.8{\pm}0.4$ mg C/L, indicating 56% mineralization of DOC. In soil-derived solution 2 (initial DOC = 19.80 mgC/L), DOC was mineralized drastically within 13 days, and the DOC concentration was decreased to $6.0{\pm}0.4$ mg C/L at 56 days (76% mineralization of DOC). Unlike DOC value, the specific UV absorbance ($SUVA_{254}$) value, an indicator of proportion of aromatic structures in total organic carbon, tended to increase until 21 days and then decreased thereafter. The $SUVA_{254}$ values in soil-derived solutions 1 and 2 were the highest at 21 days. The microbial analysis demonstrated that Pseudomonas fluorescens, Achromobacter xylosoxidans, Nocardioides simplex, Pseudomonas mandelii, Bosea sp. were detected at 14 days of incubation, whereas Pseudomonas veronii appeared as a dominant species at 56 days.

• Proceedings of the Korean Society of Grassland Science Conference
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• 2002.09a
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• pp.28-28
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• 2002

• Economic and Environmental Geology
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• v.35 no.2
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• pp.149-154
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• 2002

Column tests were carried out to examine the effect of surfactant solution conditions on surfactant-enhanced remediation of contaminated soil. The selected conditions of the surfactant solution were concentration and pH. 1,2,4-trichlo-robenzene (TCB) was chosen as the model hydrophobic organic substances. Sodium diphenyl oxide disulfonate (DOSL) and octylphenoxypoly ethoxyethanol (OPEE) surfactants were selected for this study. Two Iowa soils, Fruitfield sand and Webster clay loam, were leached with surfactant solution. The test results revealed that an optimum condition was achieved for 4 %(v/v) of concentration and 10 of pH, respectively. The maximum recoveries of added TCB (93-98%) were obtained when optimal conditions of each surfactant solution parameter were simultaneously met. The optimum conditions of these parameters may be useful for surfactant-assisted remediation in soil contaminated by TCB.

• Korean Journal of Environmental Agriculture
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• v.24 no.3
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• pp.253-260
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• 2005

Salt accumulation in the plastic film house soils under continuous cultivation condition causes problems such as salt damages to plants, nitrate accumulation in vegetables, groundwater contamination, etc. due to excess application of fertilizers. Objective of this research was to find an optimum adsorbent to reduce salt concentration in the soil solution of plastic film house soils, where crop injuries have been observed due to the salt accumulation. The soils were significantly high in available P $(1,431{\sim}6,516mg\;kg^{-1}),\;NO_3-N\;(117.60{\sim}395.73mg\;kg^{-1})$, exchangeable Ca $(4.06{\sim}11.07\;cmol_c\;kg^{-1})$ and Mg $(2.59{\sim}18.76\;cmol_c\;kg^{-1})$, as compared to those of the average upland soils in Korea. Soils were treated with each of adsorbent such as ion-exchange resin, zeolite, rice bran, etc. at 2% level and prepared into saturated-paste samples. After equilibrium, soil solution was vacuum-extracted from the soil and measured for changes of the pH, EC, and concentrations of $Ca^{2+},\;Mg^{2+},\;K^+,\;Na^+,\;{NH_4}^+,\;{PO_4}^{3-}\;and\;{NO_3}^-$. Rice bran effectively removed ${PO_4}^{3-}\;and\;{NO_3}^-$ in the soil solution up to 100%. Efficiency was decreased in the orders of rice bran > ion-exchange resin > zeolite. Removal efficiencies of zeolite and ion-exchange resin for $Ca^{2+}$ were ranged from 1 to 65% and from 7 to 61%, respectively. Ion-exchange resin was also effective for removing $Mg^{2+},\;K^+,\;Na^+,\;and\;{NH_4}^+$. Overall results demonstrated that rice bran and ion-exchange resin could be applicable for salt accumulated soil to remove the respective anion and cation.

• Journal of Soil and Groundwater Environment
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• v.8 no.1
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• pp.17-26
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• 2003

The sorption experiment of cobalt was performed after the TRIGA soil was intentionally contaminated with cobalt was found that the sorption equilibrium coeficiency of soil decontamination was high when the ratio of soil mass to the volume of citric acid becomes 1:5 The TRIGA soil contaminated with 0.01 M, 0.001 M, and 0.0001 M of cobalt solution were decontaiminated with 0.01 M citric acid. The cobalt concentrtion in the wastewater were measured to be correspondingly 36.0, 14.0, 1.5 ppm. The results of wastewater recycling experiment by chemical precipitation method revealed that corresponding cobalt removal efficiency were 97% 88%. It was shown that the removal efficiency decreases as the cobalt concentration in the wastewater decreases. During the decontamination experiment, a lot of NaOH had to be added, and the volume of final solid waste reached almost 10% of that of the contaminated soil. The result of wastewater recyling experiment by ion exchange resin meted rethod revealed that to more the strong acid resins are used, the higher the cobalt removal efficiency becomes and the cobalt removal efficiency becomes and the lower the pH of recycling wastewater become. In order to obtain more than 95% removal efficiency, more than 0.625 g of strong acid resin was necessary in each of 3 experiments. There was an unexpected problem that a lot of strong acid resin waste was produced which amounts to 9.2% (volume) of the contaminated soil.

• Korean Journal of Soil Science and Fertilizer
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• v.10 no.2
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• pp.75-78
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• 1977

Corn (Zea may, L.) was grown alternatively in nutrient solution and hydroxy Al or Al-citrate solution to identify the form of Al which induces Al toxicity on Corn seedlings. Corn seedlings exposed to hydroxy Al solution was very toxic but Al-citrate solution did not show any toxic symptoms. At pH 7 with Al-citrate solution, severe Fe, deficiency was induced probably by the decrease of stability constant of Al-and Fe-oganic complexes and subsequent precipitation of Al-and Fe-as a hydroxide form. Addition of humic acid ameliorated the Al toxicity somewhat at pH 4.7 with hydroxy-Al solution but at pH 7 it induced more severe Fe deficiency.

• Analytical Science and Technology
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• v.29 no.6
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• pp.261-268
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• 2016

TXRF is a powerful technique for the soil sample analysis due to its ability to conduct quantitative analysis of powder sample without complicated pre-treatment processes. The conventional internal standard method used for this technique suffers from relatively low accuracy because of varying matrix effects of soil. In order to improve the accuracy, external standard method was applied to analyze two types of soil samples; acid-dissolutionized soil solution and detergent-suspended soil powder. Individual ICP-AES/MS grade standards were mixed, diluted and measured to create standard curves, but applying these curves for analyzing the soil solution sample did not make any improvement in comparison with the internal standard method. On the other hand, standard curves were created with using standard soil powders for the analysis of soil powder samples, and we found that this method increased the accuracy significantly relative to the internal standard method. Especially, Al, Fe, K, Ca, Ti, Ba, Mn, Sr, Rb, Cu was measured with relatively high accuracy (relative error = ${\pm}20%$).

• Korean Journal of Soil Science and Fertilizer
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• v.24 no.2
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• pp.116-123
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• 1991

Two solution to soil ratios, 2 : 1 and 5 : 1 were tested to determine the appropriate ratio in the sorption measurement off. sulfoxide for Wahiawa soil samples, 0-20 cm, 40-60 cm and 100-120 cm. and Salinas soil samples, 0-15cm and 115-130cm. One ${\mu}$ mol/L f.sulfoxide was used as an initial equilibration concentration. Sorption of f.sulfoxide at 5 : 1 ratio showed appropriate mixing, while sorption at 2 : 1 ratio indicated insufficient mixing during the various batch equilibration times (4, 12, 24 and 48 hours). For most samples the degree of sorption was about 20-50%, which falls in the desired range (20-80%) at the 5 : 1 ratio. An exception was with the low-sorptive Wahiawa subsoil in which the ranges were below 20%. Thus the 5 : 1 ratio can be used for f.sulfoxide sorption measurement. Four equilibration times (4, 12, 24 and 48 hours) and four concentrations(0.1, 1.0, 5.0 and $10{\mu}mol/L$) were used to determine the appropriate equilibration time for Wahiawa and Salinas soils. Sorption increased over all equilibration times, indicating no complete equilibrium within 48 hours. Apparent equilibrium was reached in 4 hours, and sorption increased slowly until 24 hours and faster thereafter, except for the Wahiawa soil, 100-120 cm. The recommended equilibration time is 24 hours, since it may eliminate the insufficient sorption and yet avoid undesirable transformation.