• Journal of Korean Society of Environmental Engineers
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• v.27 no.10
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• pp.1058-1064
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• 2005

This research was designed to investigate the removal of anionic species, such as $F^-$, $Cl^-$ and ${NO_3}^-$, by adsorption on the clay minerals. Bentonite, $Ca^{2+}$ or $Na^+$ ion exchanged bentonite and montmorillonite, such as KSF and K10 from Sigma Aldrich, were used as the adsorbent. The component of five inorganic adsorbent was analyzed by XRF and XRD and the concentration of anion was measured by ion chromatography. From the experimental results, it was shown that the adsorption equilibrium was attained after 8-24 hours. For the amount of 6 g of each adsorbent, the adsorption capacities of $F^-$ and ${NO_3}^-$ on KSF was the largest as $825\;{\mu}g/g$ and $707\;{\mu}g/g$ respectively and that of $F^-$ on $Ca^{2+}$ ion exchanged bentonite was $255\;{\mu}g/g$ and that of ${NO_3}^-$ on K10 was $103\;{\mu}g/g$. In general, the efficiency of removal for the anionic species was increased with increasing of the amount of the adsorbent. Especially, for the amount of 6 g of KSF, the efficiency of removal for $F^-$ and ${NO_3}^-$ was 99% and 95% respectively. But, for all adsorbents, the efficiency of removal for $Cl^-$ was less than 9%. Also, a Freundlich equation was used to fit the acquired experimental data. As the result, for the $F^-$ and ${NO_3}^-$ on KSF, Freundlich constants, K, was respectively 1.09 and $0.45\;[mg/g][L/mg]^{1/n}$ and the adsorption intensity(1/n) was determined to be 0.08 and 0.27 respectively.

• Environmental Engineering Research
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• v.21 no.2
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• pp.203-210
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• 2016

Hybrid materials were obtained modifying the bentonite (BC) and local clay (LC) using hexadecyltrimethylammonium bromide (HDTMA) or the clay were pillared with aluminum followed by modification with HDTMA. The materials were characterized by the SEM, FT-IR and XRD analytical tools. The batch reactor data implied that the uptake of $17{\beta}$-estradiol (E2) by the hybrid materials showed very high uptake at the neutral pH region. However, at higher and lower pH conditions, slightly less uptake of E2 was occurred. The uptake of E2 was insignificantly affected changing the sorptive concentration from 1.0 to 10.0 mg/L and the background electrolyte (NaCl) concentrations from 0.0001 to 0.1 mol/L. Moreover, the sorption of E2 by these hybrid materials was fairly efficient since within 30 mins of contact time, an apparent equilibrium between solid and solution was achieved, and the data was best fitted to the PSO (pseudo-second order) and FL-PSO (Fractal-like-pseudo second order) kinetic models compared to the PFO (pseudo-first order) model. The fixed-bed column results showed that relatively high breakthrough volume was obtained for the attenuation of E2 using these hybrid materials, and the loading capacity of E2 was estimated to be 75.984, 63.757, 58.965 and 49.746 mg/g for the solids BCH, BCAH, LCH and LCAH, respectively.

• The Journal of Natural Sciences
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• v.13 no.1
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• pp.35-50
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• 2003

Granular clay minerals for adsorption of the organic dye prepared a Na-Bentonite and optimum condition calcined temperature $700^{\circ}C$ and polyvinyl alcohol quantity was 25%. Granular clay mineral stable range was pH3 to pH9 and specific area was $83m^2/g$. The adsorption of the organic dye on the Granular clay mineral showed result good adsorption with acid medium and then enthalpy was -3.36 ~ -0.84 kcal/mol. It was exhibit typical physical adsorption.

• Journal of the Mineralogical Society of Korea
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• v.7 no.2
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• pp.111-127
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• 1994

양남 지역의 제 3 기층인 하서리 응회암층의 중.상부에 부존되는 벤토나이트들은 원암의 암상과 화학조성에 의존되는 광호 양상과 광물상을 나타낸다. 벤톤나이트들은 대부분 안산암질 원암의 기원을 시사하는 희유 및 희토류 원소들의 함유 양상을 보이고, 현무암질 원암의 벤토나이트는 최상부의 일부 층준에만 그 산출이 국한된다. 이 지역의 벤토나이트는 주로 유리질 내지 라필리 응회암이 속성 변질된 것으로 이 과정에서 SiO2와 알칼리 (Na, K) 성분들이 고갈되는 화학 성분상의 유동 양상이 인지된다. 벤토나이트는 주된 광물 성분인 스멕타이트 이외에 흔히 단백석 및 석영같은 규산 광물과 휼란다이트, 모데나이트 및 클리높틸로라이트간은 불석광물들을 수반한다. 스멕타이트는 대부분 몰노릴로나이트 유형이지만 최상부 층준의 현무암질원 벤토나이트와 비교하여 논트로나이트의 광물 화학, X-선회절 양상, 층간 화학 및 염화학적 특성 등이 논의되었다. 이 지역 벤토나이트의 형성과정은 (1) 화산쇄설물의 급속한 퇴적, (2) 비이상적으로 높은 매몰 온도(<8$0^{\circ}C$) 조건, (3) 규산 광물의침전에 의한 공극수 내외 H4SiO4의 제거, (4) 원암의 낮은 Si/al 함유비와 높은 Fe 함유도 등에 의해서 조장된 것으로 해석된다.

• Proceedings of the Korean Geotechical Society Conference
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• 2008.03a
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• pp.938-946
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• 2008

This study is on sealing leakage holes where are in landfills to make clay cakes with clay particles, which have a negative surface charge using the method of electrophoresis. Generally, electrophoresis is the motion of charged particles in a colloid under the influence of an electric field; particles with a positive charge go to the cathode and negative to the anode. In this study in order to develop the prevention system of leakages of the leachate in landfills, one-dimensional electrophoresis tests were conducted for determining the properties of the motion of the electrophoresis and cutoff using the method of electrophoresis depending on various the effect factors such as types of clays, concentrations of the clays, and applied electric field. In case of the experiments of determining the optimum clays, Na and Ca-Bentonite, Na and Ca-Montmorillonite, which have greater zeta-potential, cation, exchange capacity as well as ability of cutoff, and Micro-cement inducing cementation were chosen and then the effect of those clays was investigated. Moreover, the properties of the motion and settling of the clays were investigated following electric field varied from 0 to 1V/cm at different concentration of the clays in order to determine both the properties of the motion of the clays and the efficiency of electric field when applying different direct current. Ultimately, the ability of cutoff was examined through measuring the permeability of the clay cakes derived from the one-dimensional electrophoresis tests.

• Journal of the Korean Geotechnical Society
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• v.23 no.2
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• pp.29-34
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• 2007

This study examines the effects of heat treatment under laboratory conditions for mixtures of two types of clay (kaolinite and montmorillonite). Clay samples were burned with different temperatures ranging from $100^{\circ}C\;to\;500^{\circ}C$. The Atterberg limits such as liquid and plastic limits were influenced with heat treatment. According to the experimental results, the liquid limits slightly decreased between $100^{\circ}C\;to\;300^{\circ}C$, whereas rapid decreases were observed after $300^{\circ}C$. The plastic limits did not show noticeable differences in the interval $100^{\circ}C\;to\;400^{\circ}C$. But the clay samples showed non plastic behavior at $500^{\circ}C$. The amount of NaCl was getting decreased with temperature. It also revealed that the pH values were also influenced with heat treatment, and the cation exchange capacity (C.E.C) values decreased with temperature.

• Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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• v.16 no.2
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• pp.261-270
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• 2018

In this study, to replace the 'J-slot joint', a joint device between a disposal canister and an emplacement jig in Deep Borehole Disposal process, a novel joint device was designed and tested. The novel joint device was composed of a wedge on top of a disposal canister and a hook box at the end of a winch system. The designed joint device had merits in that it can recombine an emplaced canister freely without the replacement of the joint component. Moreover, it can be applied to various emplacement jigs such as drill pipes, wire-lines, and coiled tubing. To demonstrate the designed joint device, the joint device (${\Phi}110mm$, H 148 mm), a twin canister string (${\Phi}140mm$, H 1,105 mm), and a water tube (${\Phi}150mm$, H 1,500 mm) as a borehole model were manufactured at 1/3 scale. As deployment muds, Na-type bentonite (MX-80) and Ca-type (GJ II) bentonite muds were prepared at solid contents of 7wt% and 28wt%, respectively. The manufactured joint device showed good performance in pure water and viscous muds, with an operation speed of $10m{\cdot}min^{-1}$. It was concluded that the newly developed joint device can be used for the emplacement and retrieval of a deep disposal canister, below 3~5 km, in the future.

• Journal of The Korean Society of Grassland and Forage Science
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• v.36 no.3
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• pp.191-198
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• 2016

This study evaluated the effects of TMC (trace mineral-fortified microbial culture) supplementation on growth performance, carcass characteristics, and meat quality parameters of Hanwoo steers during the last 4 months of finishing period. The TMC was a combination of 0.4% trace minerals, 20.0% Na-bentonite, and 79.6% feedstuffs, which was inoculated with a mixed microbial culture (Enterobacter ludwigii, Bacillus cereus, B. subtilis, Lactobacillus plantarum, and Saccharomyces cerevisiae). Twenty-four steers were blocked by initial BW ($634{\pm}16kg$) and randomly allocated to one of two treatments (control vs. 3.3% TMC). The effect of TMC supplementation on the growth performance was not significant. There was no incidence of urolithiasis in TMC-fed steers. However 3 out 12 steers (25%) fed the control diet were observed to have urinary calculi. The carcass yield and meat quality parameters were not affected by TMC supplementation, however marbling score was increased in TMC-fed steers (P = 0.08). There was no effect of TMC treatment on the chemical composition of longissimus dorsi muscle (LM). The TMC supplementation increased concentrations of manganese (P < 0.01), cobalt (P = 0.02), iron, and copper (P = 0.06) in LM. In conclusion, TMC treatment did not negatively affect growth performance and meat quality parameters, and positively affected the trace minerals profile of LM.

• Proceedings of the IEEK Conference
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• 2001.10a
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• pp.586-591
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• 2001

This research investigated the feasibility of the accelerated carbonation of cement waste forms with carbon dioxide in a supercritical state. Hydraulic cement has been used as a main solidification matrix for the immobilization of radioactive and/or hazardous wastes. As a result of the hydration reaction for major compounds of portland cement, portlandite (Ca(OH)$_2$) is present in the hydrated cement waste form. The chemical durability of a cement form is expected to increase by converting portlandite to the less soluble calcite (CaCO$_3$). For a faster reaction of portlandite with carbon dioxide, SCCD (supercritical carbon dioxide) rather than gaseous $CO_2$, in ambient pressure is used. The cement forms fabricated with an addition of slated lime or Na-bentonite were cured under ambient conditions for 28days and then treated with SCCD in an autoclave maintained at 34$^{\circ}C$ and 80atm. After SCCD treatment, the physicochemical properties of cement matrices were analyzed to evaluate the effectiveness of accelerated carbonation reaction. Conversion of parts of portlandite to calcite by the carbonation reaction with SCCD was verified by XRD (X-ray diffraction) analysis and the composition of portlandite and calcite was estimated using thermogravimetric (TG) data. After SCCD treatment, tile cement density slightly increased by about 1.5% regardless of the SCCD treatment time. The leaching behavior of cement, tested in accordance with an ISO leach test method at 7$0^{\circ}C$ for over 300 days, showed a proportional relationship to the square root of the leaching time, so the major leaching mechanism of cement matrix was diffusion controlled. The cumulative fraction leached (CFL) of calcium decreased by more than 50% after SCCD treatment. It might be concluded that the enhancement of the characteristics of a cement matrix by an accelerated carbonation reaction with SCCD is possible to some extent.

• Journal of the Mineralogical Society of Korea
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• v.15 no.4
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• pp.329-344
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• 2002

Mineralogical and chemical characterization of some domestic bentonites, such as quantitative XRD analysis, chemical leaching experiments, pH and CEC determinations, were done without any separation procedures to understand their relationships among mineral composition, characteristics, and cation exchange properties. XRD quantification results based on Rietveld method reveal that the bentonites contain totally more than 25 wt% of impurities, such as zeolites, opal-CT, and feldspars, in addition to montmorillonite ranging 30～75 wt%. Cation exchange properties of the zeolitic bentonites are deeply affected by the content of zeolites identified as clinoptilolite-heulandite series. Clinoptilolite is common in the silicic bentonites with lighter color. and occurs closely in association with opal-CT. Ca is mostly the dominant exchangeable cation, but some zeolitic bentonites have K as a major exchangeable cation, The values of cation exchange capacity (CEC) determined by Methylene Blue method are comparatively low and have roughly a linear relationship with the montmorillonite content of the bentonite, though the correlated data tend to be rather dispersed. Compared to this, the CEC determined by Ammonium Acetate method, i.e.‘Total CEC’, has much higher values (50～115 meq/100 g). The differences between those CEC values are much greater in zeolitic bentonites, which obviously indicates the CEC increase affected by zeolite. Other impurities such as opal-CT and feldspars seem to affect insignificantly on the CEC of bentonites. When dispersed in distilled water, the pH of bentonites roughly tends to increase up to 9.3 with increasing the alkali abundance, especially Na, in exchangeable cation composition. However, some bentonites exhibit lower pH (5～6) so as to regard as ‘acid clay’. This may be due to the presence of $H^{＋}$ in part as an exchangeable cation in the layer site of montmorillonite. All the works of this study ultimately suggest that an assesment of domestic bentonites in grade and quality should be accomplished through the quantitative XRD analysis and the ‘Total CEC’measurement.