• Journal of the Korean Chemical Society
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• v.27 no.3
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• pp.178-182
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• 1983

The conductances of sodium, potassium, ammonium, tetramethylammonium, and tetraethylammonium iodides, picrates(Pic) of sodium and potassium, and tetrabutylammonium tetraphenyl-boride have been measured in ethylene carbonate-acetone mixtures at $25{\circ}C$. The limiting equivalent conductances of the electolytes were computed by Fuoss-Kraus equation and the order was $(C_4H_9)_4NB(ph)_4 at any composition of the mixtures. The dissociation constants of the salts showed that the mixtures are good ionizing solvents for the salts. The order of limiting ionic equivalent conductance, $Na^+, is consistent with exactly the reverse order found for solvation number. Effective solvated radii calibrated by the Nightingale method showed that picrate ion seems to be unsolvated and that iodide ion seems to be solvated to some extent in the mixtures.

• Journal of Korean Society of Environmental Engineers
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• v.37 no.4
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• pp.197-203
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• 2015

Particulate matter (PM) has emitted in many regions of the world and is causing many health-related problems. Thus reasonable politics and solutions are needed to reduce PM in Seoul. Further it is required to clearly explain the major portions of chemical components contained in $PM_{10}$ to figure out the characteristics of $PM_{10}$, and to develop effective reduction measures in order to decrease the adverse effects of $PM_{10}$. $PM_{10}$ samples were collected in Seoul and analyzed their ions to examine the physical and chemical characteristics of ionic species. Since hydrogen ion ($H^+$) and carbonate ion (${CO_3}^{2-}$)) cannot be analyzed by Ion chromatography (IC), concentrations of $H^+$ and ${CO_3}^{2-}$ were initially estimated by pH and equivalent differences between anions and cations in this study. Starting from the study findings, good combination results for compositional patterns between anions and cations were obtained by applying a mathematical modelling technique that was based on the mass balance principle. The ions in $PM_{10}$ were combined with $H^+$, ${CO_3}^{2-}$, and supplement for $NO_3{^-}$, $Cl^-$ formed such compounds $NH_4Cl$, $NH_4NO_3$, $CaSO_4$, $(NH_4)_2SO_4$, $NaNO_3$, NaCl, $Na_2CO_3$, and $(NH_4)_2CO_3$ in the study area.

• Proceedings of the Korean Radioactive Waste Society Conference
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• 2010.05a
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• pp.143-144
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• 2010

• Applied Chemistry for Engineering
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• v.34 no.2
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• pp.111-120
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• 2023

The nucleation mechanism was studied using a calcium ion selective electrode (Ca ISE) to observe the formation of CaCO₃, a representative mineral in the CO2 cycle, and to analyze the effect of the Mg/Ca-ratio and temperature on the formation of pre-nucleation cluster (PNC) and CaCO₃. As a result of the experiment, a small amount of crystal was formed. Energy dispersive X-ray spectroscopy (EDS) was used for surface element analysis, and a field emission scanning-electron microscope (FE-SEM) was used for the morphology analysis of synthesized carbonates. These results showed that various shapes of crystalline CaCO₃ (calcite, aragonite, etc.) were observed for each Mg/Ca ratio and temperature. In addition, the calibration plot obtained from Ca ISE showed information on the formation process of CaCO₃. Our results showed that as magnesium ions interfered with the binding of calcium and carbonate ions and delayed the aggregation between PNCs, the nucleation and formation of CaCO₃ were delayed. On the other hand, the temperature showed an opposite trend as compared to the effect of magnesium under our experimental conditions, indicating that temperature accelerated the formation of CaCO₃. Furthermore, the morphology of CaCO₃ clearly changed according to the Mg/Ca ratio and temperature, and it was confirmed that the two factors are very important for CaCO₃ formation in that they could affect the overall process.

• Resources Recycling
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• v.31 no.4
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• pp.26-33
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• 2022

Owing to the demand for lithium-ion batteries, the recovery of valuable metals from waste lithium-ion batteries is required in future. A pyrometallurgical treatment is appropriate for recycling a large number of waste lithium-ion batteries, but Li loss to slag and dust present a significant challenge. This research investigated carbonation roasting and water leaching behaviors in Li-ion batteries by graphite addition to recover Li from the NCM-based cathode materials of waste Li-ion batteries. When 10 wt% of graphite was added, CO and CO₂ gases were emitted with a rapid weight reduction at apporoximately 850 K, when heated in Ar and CO₂ atmosphere. After the rapid weight reduction, NCM was decomposed and reduced to metal oxides and pure metals. In the carbonation roasting of black powder (NCM+graphite), O₂ is generated via the decomposition of NCM, and an oxides, such as Li₂O and NiO were were also generated. Subsequently, Li₂O reacts with CO₂ to generate Li₂CO₃, and a part of NiO was reduced by graphite to produce metal Ni. In addition, up to 94.5 % Li₂CO₃ with ~99.95 % purity was recovered via water leaching after carbonation roasting.

• The Sea:JOURNAL OF THE KOREAN SOCIETY OF OCEANOGRAPHY
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• v.24 no.3
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• pp.389-399
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• 2019

The calcium carbonate saturation state in the Ulleung Basin of East Sea was calculated using bottle data set of pH, dissolved inorganic carbon and total alkalinity obtained from the year 1999, 2014, 2017, and 2018 cruise. In the 2010s calcium carbonate saturation state was significantly lowered at all depth compared to the 1999 reference state. Accordingly calcite saturation horizon and aragonite saturation horizon shoaled to 500 m and 200 m, respectively. A key chemical species for the calcium carbonate saturation state, carbonate ion showed distinctive profile between upper and deep waters: it is moderately high (${\sim}175{\mu}mol\;kg^{-1}$) in upper waters and very low (< ${\sim}50{\mu}mol\;kg^{-1}$) in the deep waters. However the decreasing trend of carbonate ion concentration was pronounced in the upper water than deep waters, suggesting atmospheric $CO_2$ penetration is largely confined to the upper waters in the 2000s.

• Journal of the Korea Institute of Building Construction
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• v.23 no.4
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• pp.349-358
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• 2023

This research aimed to enhance the initial strength of concrete that is mixed with ground granulated blast furnace slag, as well as to fortify its resistance to carbonation and chloride ion permeation. To achieve this, alkaline aqueous, produced through the electrolysis of potassium carbonate, was employed as the mixing water in the preparation of concrete. To substantiate the increment in initial strength, compressive strength measurements of the concrete were executed. Additionally, an accelerated carbonation test and a chloride ion permeation resistance test were undertaken. The results confirmed that the initial strength of the concrete, which utilized electrolysis alkaline aqueous as mixing water, exhibited an improvement in comparison to concrete mixed with conventional water. It was also verified that both carbonation resistance and chloride ion permeation resistance showed enhancements.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.6 no.4
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• pp.509-520
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• 1996

Ultrafine calcim carbonate powders with the size of $0.05~0.1\;{\mu}m$ and the calcite phase were synthesized by the nozzle spouting method, which could be only obtained when high calcium ion concentration within slurry was maintained at the beginning of the reaction. But, in the regions of low ${Ca(OH)}_2$ concentration (0.5~1.0 wt%) or high ${Ca(OH)}_2$ concentration (<3.0 wt%), synthesized calcium carbonate powder was shown the large particle size with agglomeration. To obtain ultrafine calcium carbonate powder in this region, the methods of slurry circuation and $CO_{2}$ gas supply were changed during reaction. Resultly, it was possible to synthesize ultrafine particles (${\approx}0.05{\mu}\textrm{m}$)in the regions of low ${Ca(OH)}_2$ concentration (${\approx}0.5wt%$) and high ${Ca(OH)}_2$ concentration (${\approx}0.5wt%$), which can not be obtained the fine calcium carbonate powder still now.

• Proceedings of the Korea Society for Energy Engineering kosee Conference
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• 1995.11a
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• pp.71-74
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• 1995

티타니아계의 흡착제로 최근 주목을 끄는 것은 티탄산칼륨 신소재를 들을 수 있다. 모서리의 chains sharing들과 b축을 따라서 TiO$_{6}$, 즉 8면체의 coner 결합으로 특징 지워지는 티탄산칼륨은 $K_2$O.nTiO$_2$로 표시되는 화합물로 플라스틱의 보강재나 단열재료 용도로 사용되었다. 공업재료로서 중요한 것은 n의 값이 2, 4, 6으로 각각 2티탄산칼륨(K$_2$Ti$_2$O$_{5}$), 4티탄산칼륨(K$_2$Ti$_4$O$_{9}$), 6티탄산칼륨(K$_2$Ti$_{6}$O$_{13}$)으로 불린다. 티탄산칼륨은 기계적 강도가 고강도재료 지르코이나에 해당하고 선팽창계수는 알루미나보다 작아 우수한 내열 및 단열 고강도재료이며 융막재, 이온교환재등으로 쓰인다. 층상구조의 티탄산칼륨을 산처리하여 칼륨을 추출하고 수소이온으로 치환한 결정질 티탄산칼륨 섬유(H$_2$Ti$_4$O$_{9}$.1.2~1.3$H_2O$)는 (H$^{-}$. H$_3$O$^{+}$)Ti$_4$O$_{9}$의 형태를 지니게 된다.

• Journal of the Korean Geotechnical Society
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• v.37 no.4
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• pp.39-47
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• 2021

Recently, the enzyme-induced carbonate precipitation (EICP) technique has been considered as one of the alternatives to the cement-based soil reinforcing method. However, the problem with the emission of ammonium ion has not been solved. In this study, an experimental study on the EICP without releasing an environmental contaminant (Ze-EICP) is performed using calcium-exchanged zeolite. The results show that the Ze-EICP using calcium-exchanged zeolite reduced the amount of ammonium ions by 96.96% and precipitated almost the same amount of calcium carbonate, compared to the EICP using calcium chloride. In addition, the Ze-EICP shows higher strength improvement rate than the EICP due to densification of zeolite and cementation of calcium carbonate.