• Economic and Environmental Geology
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• v.33 no.1
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• pp.31-40
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• 2000

Sorption characteristics of Pb, Cu, Cd, and Zn onto Ca- and Na-bentonites were investigated by the batch experiments in the condition of various pHs and concentrations of groundwater major anions (${So_4}^{2-}$ and ($HCO_3$), which can form a complex with heavy metals. The sorption removal of heavy metals steadily increases as pH increases. The sorption capability about heavy metals of both Ca-bentonite and Na-bentonite is in the order of Pb>Cu>Zn>Cd. The effect of pH and selectivity of heavy metals of bentonites were explained by the change of surface charge of bentonite and the speciation of heavy metals. Na-bentonite has a little higher sorption ability about heavy metals than that of Ca-bentonite. A high sorption removal of Pb in 0.1M sulfate solution may be attributed to the precipitation of $PbSo_4$(anglesite). However, sulfate has a slight effect on the sorption of CU, Cd and Zn. More than 99% of heavy metals were removed from the 0.1 M bicarbonate solution. However, the efficiency of sorption removal of heavy metals highly decreases in the bicarbonate solution of $10^{-2}$M to $10^{-4}$M. The speciation and saturation index calculated by the WATEQ4F program indicate that the sorption of anionic complexes such as ${Pb(CO_3)_2}^{2-}$, ${Cd(CO_3)_2}^{2-}$, ${Zn(CO_3)_2}^{2-}$, ${Cu(CO_3)_2}^{2-}$ and the precipitation of the solid phases such as $PbCO_3$(cerrusite), $ZnCO_3$(smithsonite), $CdCO_3$(obtavite) are involved in sorption removal of heavy metals in bicarbonate solution. The sorption capability about heavy metals of bentonites in the presence of anions shows the following order: Pb>Cu Cd>Zn.

• Korean Chemical Engineering Research
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• v.50 no.6
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• pp.994-1001
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• 2012

The Effects of operating variables on reactivity of two $CO_2$ absorbents (PKM1-SU and P4-600) for SEWGS process were investigated in a pressurized fluidized bed reactor. For both $CO_2$ absorbents, $CO_2$ sorption capacity decreased as the number of absorption-regeneration cycles increased. PKM1-SU absorbent represented higher $CO_2$ sorption capacity than that of P4-600 absorbent. However, P4-600 absorbent represented better performance than PKM1-SU absorbent from the view points of regeneration temperature and regeneration rate. For PKM1-SU absorbent, $CO_2$ sorption capacity increased as the steam concentration increased. However, $CO_2$ sorption capacity increased initially as the steam concentration increased from 5% to 10%, but maintained thereafter for P4-600 absorbent. For both $CO_2$ absorbents, $CO_2$ sorption capacity increased as the final regeneration temperature increased. For PKM1-SU absorbent, $CO_2$ sorption capacity increased as the pressure increased and the increment tendency was drastic at higher pressure than 15 bar.

• Nuclear Engineering and Technology
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• v.32 no.4
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• pp.342-349
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• 2000

A soil whose texture is silt loam was collected for the study from an area around a nuclear facility in Korea. The equilibrium sorption coefficient between Co$^{2+}$in water and the soil was 1.51/kg, on the other hand, that between Co$^{2+}$ in EDTA and the soil was 0.21/kg. The values calculated by the developed nonequilibrium sorption code corresponded to the experimental values better than those calculated by the existing equilibrium sorption code. When an EDTA solution was used as a solvent to decontaminate Co$^{2+}$ in the soil column, the relative Co$^{2+}$ concentrations of the effluent were higher at 2~10 pore volumes than those of the case using water. The soil in the column was decontaminated by 95.5% of the total amount of Co$^{2+}$ after being flushed with EDTA solution of 20 pore volumes.e volumes.

• KEPCO Journal on Electric Power and Energy
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• v.5 no.4
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• pp.337-341
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• 2019

In this study, the effects of two materials, active alumina and CaO based inorganic binder, which cause the side reaction on the K₂CO₃-based solid CO₂ sorbents was investigated. K₂CO₃-based solid sorbents called KAM series was prepared by spray drying method and then measured its physical properties and CO₂ sorption capacity. Among the KAM series sorbents, KAM(0.5) maintained high CO₂ sorption capacity of 7.6 wt% after 3 cycle of sorption/regeneration reaction and showed very low attrition loss as low as 3.1 % which was measured by ASTM D5757-95.

• Transactions of the Korean hydrogen and new energy society
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• v.14 no.4
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• pp.321-326
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• 2003

We tried to improve the $H_2$-sorption properties of Mg by mechanical grinding under $H_2$ (reactive grinding) with CoO. The sample Mg+10wt.%CoO as prepared absorbs 1.25wt.% hydrogen and the activated sample absorbs 2.39wt.% hydrogen for 60min at 598K, $11.2barH_2$. The reactive grinding of Mg with CoO increases the $H_2$-sorption rates by facilitating nueleation(by creating defects on the surface of the Mg particles and by the additive), by making cracks on the surface of Mg particles and reducing the particle size of Mg and thus by shortening the diffusion distances of hydrogen atoms. Hydriding-dehydriding cycling increases the $H_2$-sorption rates by making cracks on the surface of Mg particles and reducing the particle size of Mg.

• Journal of Nuclear Fuel Cycle and Waste Technology
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• v.1 no.1
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• pp.57-63
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• 2013

Natural green rust (GR) can retard the migration of anions through geological media because it has a Layer Double Hydroxyl (LDH) structure with a positive charge. In this study, the sorption behaviors of anions such as selenite ($Se(IV)O{_3}^{2-}$), selenate ($Se(VI)O{_4}^{2-}$), and iodide ($I^-$) onto green rusts with different structures, i.e., GR($Cl^-$) and GR($CO{_3}^{2-}$), were investigated by conducting batch sorption experiments in an anoxic condition. Experimental results showed that selenite was mostly sorbed onto GR($CO{_3}^{2-}$) and then partly reduced to metal selenium, Se(0). However, little selenate and iodide was sorbed onto GR($CO{_3}^{2-}$) while some iodide was sorbed onto GR($Cl^-$). It is presumed from the experimental results that the major sorption mechanism of $SeO{_3}^{2-}$ and $I^-$ onto green rusts is the anion exchange reaction with the anions existing in the interlayer of the rusts. Green rust, therefore, can play an important role in the retardation of anions migrating through deep geological environments owing to its LDH structure with a high anion exchange capacity.

• 한국신재생에너지학회:학술대회논문집
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• 2009.06a
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• pp.745-748
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• 2009

수소는 지구상에 풍부하게 존재하는 원소로 최근 수소경제시대에 대한 기대와 함께 청정 에너지 carrier로 주목받고 있다. 본 연구에서는 고순도 수소 생산을 위해 water gas shift (WGS) 반응과 $CO_2$의 분리를 하나의 unit operation의 형태로 수행하는 신개념의 thermal swing sorption enhanced reaction (TSSER) 공정의 타당성을 테스트하는데 목적을 두고 있다. Le Chatelier 원리를 기본으로 하는 흡착분리 동시 반응 (sorption enhanced reaction, SER)에서는 수소생산 반응의 열역학적 한계를 극복할 수 있고 정반응의 속도를 증대시킬 수 있다. 본 연구에서는 $K_2CO_3$가 첨가된 hydrotalcite에 대한 고온에서의 $CO_2$ 화학흡착 평형 및 거동 데이터를 실험을 통하여 측정하였다. 또한 WGS 상용촉매와 화학 흡착제를 이용하여 흡착분리 동시 반응을 실험과 수치해석 시뮬레이션으로 수행하였고, 연구결과로부터 연료전지에 사용할 수 있는 고순도의 수소 (~10 ppm CO)를 직접 생산할 수 있으며, 동시에 고압상태의 $CO_2$를 고순도로 포집할 수 있음을 확인할 수 있었다. 고압, 고순도의 $CO_2$ 포집은 이후 $CO_2$ 저장에 용이하게 이용되어 온실가스 저감에 기여할 수 있을 것으로 기대된다.

• Proceedings of the Korean Radioactive Waste Society Conference
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• 2005.06a
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• pp.485-495
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• 2005

This study was conducted to investigate sorption and desorption behaviors of radionuclides (Cobalt and Strontium) in natural soil. Sorption kinetics and isotherms were analyzed to predict sorption behaviors of radionuclides in natural soil and the experimental data were fitted to several sorption models. Desorption experiments were also performed with or without CMCD at constant pH and ion strength conditions. The results showed that $Sr^{2+}$ was more strongly sorbed than $Co^{2+}$ in natural soil. Both $Co^{2+}$ and $Sr^{2+}$ followed a pseudo-second order kinetics and Sips model. The desorption-resistance of $Co^{2+}$ and $Sr^{2+}$ was estimated using a natural surfactant Carboxymethyl-${\beta}$-cyclodextrin(CMCD) or non-desorbing fraction. Desorption of radionuclides was partially irreversible and $Sr^{2+}$ was more resistant than $Co^{2+}$ Addition of CMCD facilitated desorption of $Co^{2+}$ and $Sr^{2+}$ from soil.

• Membrane Journal
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• v.3 no.2
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• pp.79-82
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• 1993

The sorption equilibria and permeabilities for $CO_2$ in a homogeneous membrane of polystyrene with the glass transition temperature of $95^{\circ}C$ were measured at a temperature of $60^{\circ}C$ and gas pressures up to 1.6 MPa and 2.5 MPa, respectively. The sorption isotherm had the form af dual-mode sorption model at low gas pressures, but became linear at pressures above 1.3 MPa. The linear portion of the isotherm extrapolated to the origin. The pressure dependence of the rnean permeability coefficient deviated upward from the dualsrhode mobility model prediction. It was found that the glass transition was brought out by the plasticization action of sotbed $CO_2$ at a gas pressure of 1.3 MPa from the sorption isotherm. And this result was consistent with an increase in the mean permeability coefficient with applied gas pressure.

• Journal of the Korean Institute of Gas
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• v.17 no.2
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• pp.36-43
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• 2013

In order to asses gas production behavior for $CO_2$ ECBM, the sorption charcteristics on coal are considered to be a key factor. In this study, we have investigated the change of the sorption rate of adsorbed gas as a function of pressure and temperature below the appropriate depth for $CO_2$-ECBM. The experiment were carried out under four different temperatures varying from $15^{\circ}C$ to $45^{\circ}C$, while the coal pressure was varied from atmosphere to 1,400 psi for every temperature. From this results, the sorption rate both $CO_2$ and $CH_4$ increased with increasing the coal pressure. Otherwise, the sorption rate both $CH_4$ and $CO_2$ decreased linearly as the coal temperature increased. From the sensitivity studies on pressure and temperature change, it was experimentally identified that $CO_2$ sequestration rate and $CH_4$ production rate are better at deeper depths below a depth of 800 m in coal seams. However, the results showed continued decline in the increasing ratio of ECBM with formation depth.