• Title/Summary/Keyword: groundwater arsenic

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Operating parameters in electrodialysis membrane processes for removal of arsenic in groundwater (지하수내 비소제거를 위한 전기투석 막여과 운전인자 연구)

  • Choi, Su Young;Park, Keun Young;Lee, Seung Ju;Choi, Dan Bi;Park, Ki Young;Kim, Hee Jun;Kweon, Ji Hyang
    • Journal of Korean Society of Water and Wastewater
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    • v.30 no.4
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    • pp.449-457
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    • 2016
  • In this study, the effectiveness of electrodialysis in removing inorganic arsenic from groundwater was investigated. To evaluate the feasibility of the electrodialysis, operating parameters such as treatment time, feed concentration, applied voltage and superficial velocity were experimentally investigated on arsenic removal. The higher conductivity removal and arsenic removal efficiency were obtained by increasing applied voltages and operation time. An increase of salinity concentrations in arsenic polluted groundwater exerted no effects on the arsenic separation ratios. Arsenic polluted waters were successfully treated with stack voltages of 1.8 ~ 2.4 V/cell-pair to approximately 93.4% of arsenic removal. Increase flow rate in diluate cell gave positive effect to removal rate. However, increase of superficial velocity in the concentrated cell exerted no effects on either the conductivity reduction or on the separation efficiency. Hopefully, this paper will provide direction in selecting appropriate operating conditions of electrodialysis for arsenic removal.

Arsenic Removal Using Iron-impregnated Ganular Activated Carbon (Fe-GAC) of Groundwater (철침착 입상활성탄(Fe-GAC)을 이용한 지하수 내 비소 제거기술)

  • Yoon, Ji-Young;Ko, Kyung-Seok;Yu, Yong-Jae;Chon, Chul-Min;Kim, Gyoo-Bum
    • Economic and Environmental Geology
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    • v.43 no.6
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    • pp.589-601
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    • 2010
  • Recently it has been frequently reported arsenic contamination of geologic origin in groundwater. The iron-impregnated ranular activated carbon (Fe-GAC) was developed for effective removal of arsenic from groundwater n the study. Fe-GACs were prepared by impregnating iron compounds into a supporting medium (GAC) with 0.05 M iron nitrate solution. The materials were used in arsenic adsorption isotherm tests to know the effect of iron impregnation time, batch kinetic tests to understand the influence of pH, and column tests to evaluate for the preliminary operation of water treatment system. The results showed that the minimum twelve hours of impregnation time were required for making the Fe-GAC with sufficient iron content for arsenic removal, confirmed by a high arsenic adsorption capacity evaluated in the isotherm tests. Most of the impregnated iron compounds were iron hydroxynitrate $Fe_4(OH)_{11}NO_3{\cdot}2H_2O$ but a mall quantity of hematite was also identified in X-ray diffraction(XRD) analysis. The batch isotherms of Fe-GAC for arsenic adsorption were well explained by Langmuir than Freundlich model and the iron contents of Fe-GAC have positive linear correlations on logarithmic plots with Freundlich distribution coefficients ($K_F$ and Langmuir maximum adsorption capacities ($Q_m$. The results of kinetic experiments suggested hat Fe-GAC had he excellent arsenic adsorption capacities regardless of all pH conditions except for pH 11 and could be used a promising adsorbents for groundwater arsenic removal considering the general groundwater pH range of 6-8. The pseudo-second order model, based on the assumption that the ate-limiting step might be chemisorption, provided the best correlation of the kinetic experimental data and explained the arsenic adsorption system f Fe-GAC. The column test was conducted to valuate the feasibility of Fe-GAC use and the operation parameters in arsenic groundwater treatment system. The parameters obtained from the column test were the retardation actor of 482.4 and the distribution coefficient of 581.1 L/mg which were similar values of 511.5-592.5 L/mg acquired from Freundlich batch isotherm model. The results of this study suggested that Fe-GAC could be used as promising adsorbent of arsenic removal in a small groundwater supply system with water treatment facility.

Analysis of arsenic in contaminated soil SRM by two extraction methods: Ultrasonic extraction method and Microwave extraction method

  • Kim, Youn-Tae;Yoon, Hyeon;Shin, Mi-Young;Yoon, Cheol-Ho;Woo, Nam-Chil
    • Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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    • 2004.09a
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    • pp.227-230
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    • 2004
  • Two extraction techniques, Ultrasonic and Microwave extraction method, were tested for the determination of arsenic in contaminated soil SRM (Montana Soil). The extraction mixture was prepared by mixing 1 M ortho-phosphoric acid and 0.1 M ascorbic acid. This extractant was known to preserve arsenic species. The appropriate extraction time was 10 min to 20 min and the recovery rate was about 80%. A coupled system, SPE-HG-ICP-AES, was used for the determination of inorganic arsenic species. The detection limit was around 2 $\mu\textrm{g}$/1 and the linearity of calibration curve was better than $R^2$=0.99.

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Arsenic Occurrence in Groundwater of Korea (국내 지하수의 비소 산출양상)

  • Ahn, Joo-Sung;Ko, Kyung-Seok;Chon, Chul-Min
    • Journal of Soil and Groundwater Environment
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    • v.12 no.5
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    • pp.64-72
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    • 2007
  • Nationwide occurrence of arsenic in groundwater of Korea was investigated with the data from the groundwater quality monitoring stations. During 2001-2006, As has been quantitatively detected in 3.0 % of the total wells $(5.0{\sim}188{\mu}g/L)$, and its geographical distribution suggests 3 groups: an urbanized and industrialized area (Seoul and its neighbouring province), and two naturally occurring areas (Chungbuk and Gyeongnam provinces). Natural occurrence of As appears to be geologically related with Ogcheon metasedimentary rocks and Cretaceous volcanic rocks. Based on the results of the previous studies in the high As sites, the oxidation of sulfides can be a major control on As concentrations in groundwater in the mineralized and altered zone within the area of Cretaceous volcanic rocks. Desorption process under slightly high pH conditions may also be responsible for high As in groundwater in areas of Ogcheon metasedimentary rocks.

유기오염물의 분해에 의한 오염토양내 비소종 변화 영향

  • 천찬란;이상훈
    • Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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    • 2002.04a
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    • pp.347-350
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    • 2002
  • Arsenic speciation changes between As(V) and As(III) are subject to changes in accordance with redox conditions in the environment. It is common to find contaminated sites associated with mixed wastes including both organic pollutants and heavy metals. We conducted microcosm experiment under hypothesis that the co-disposed organic pollutants would influence on the arsenic forms and concentrations, via degradation of the organic pollutants and the consequent impact on the redox conditions in soil. Artificially contaminated soil samples were run for 40 days with control samples without artificial contamination. We noticed arsenic in the contaminated soil showed different behaviour compared with the arsenic in the control soil. The findings indicate degradation of organic pollutants in the contaminated soil influenced on the arsenic speciation and concentrations. A further work is needed to understand the process quantitatively. However, we could confirm that degradation of organic pollutants can influence on the abiotic processes associated with geochemical reactions in contaminated soil. Degradation of organic pollutants can increase the mobility and toxicity of arsenic in soil and sediment by changing redox conditions in the geological media and subsequently from As(V) to As(III).

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Modeling As(III) and As(V) adsorption and transport from water by a sand coated with iron-oxide colloids

  • Ko, Il-Won;Lee, Cheol-Hyo;Kim, Kyoung-Woong
    • Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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    • 2004.04a
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    • pp.243-247
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    • 2004
  • Tile development of a porous iron-oxide coated sand filter system can be modelled with the analytical solution of tile transport equation in order to obtain the operating parameters and investigate the mechanism of arsenic removal. The adsorbed amount from the model simulation showed the limitation of adsorption removal during arsenic transport. A loss reaction term in the transport equation plays a role in the mass loss in column conditions, and then resulted into the better model fitting, particularly, for arsenate. Further, the competitive oxyanions delayed the breakthrough near MCL (10 $\mu$g/L) due to the competitive adsorption. This is the reason why arsenate can be strongly attracted in tile interface of an iron-oxide coated sand, and competing oxyanions can occupy the adsorption sites. Therefore, arsenic retention was regulated by non-equilibrium of arsenic adsorption in a porous iron-oxide coated sand media. The transport-limited process seemed to be affect the arsenic adsorption by coated sand.

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Characteristics of arsenic sorption on furnace slag in groundwater

  • S. R. Kanel;Saurabh Sharma;Park, Hechul
    • Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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    • 2002.09a
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    • pp.96-98
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    • 2002
  • Furnace slag, a steel industry waste, has been converted into an inexpensive and efficient adsorbent. The product obtained has been utilized for the removal of arsenic from ground water. Kinetic studies have bepn described with the mechanism of adsorption The results from batch studies showed that the As(III) can be removed from the ground water within the pH range 3-7 However the maximum removal was experienced at pH 7.0. Equilibrium was attained within 24 hours. Adsorption data of arsenic correlate well with the Freundlich and Langmuir adsorption models. The maximum sorption capacity as calculated using Freundlich adsorption isotherm was found to be of 0.004 mg g-1 at pH 7 and $25^{\circ}C$.

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