• Elastomers and Composites
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• v.52 no.1
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• pp.81-85
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• 2017

In order to improve the water resistance, we synthesized waterborne polyurethane by using polyester polyol, poly(propylene carbonate) (PPC), 4,4'-dicyclohexylmethane diisocyanate ($H_{12}MDI$), and dimethylolpropionic acid (DMPA). The properties of the synthesized waterborne polyurethane using poly(propylene carbonate) (WPUP) were evaluated by FT-IR, $^1H-NMR$, GPC, DSC, TGA, and UTM. The mechanical properties increased while the adhesion properties decreased with the increase in the amount of PPC. The highest water resistance was shown when the ratio of polyester polyol to PPC was 9:1.

• Journal of the Korean earth science society
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• v.35 no.5
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• pp.305-312
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• 2014

A number of coated grains (spherical to elongated ones in shape) were collected from a small stream, Dijon, France. They were characterized by typical concentric lamination surrounding broken twigs, and were thus identified as concentric precipitation on plant twigs. Within carbonate coatings of the plant twigs, two morphological groups including, eukaryotic green algae (Vaucheria sp.) and cyanobacteria (Scytonema sp. and Rivularia sp.) were detected, which form carbonate crystals that are surrounding their filaments. The filaments could have triggered carbonate precipitation by photosynthetic removal of $CO_2$ causing the increase of alkalinity of the water, and by supporting their sheaths as nucleation sites. Such encrusted twigs were found from 70 meters downstream, in which temperature and pH were measured as $11.1^{\circ}C$ and 8.18, respectively. These water chemistries ($11.1^{\circ}C$ and pH 8.18), with the aid of microbial photosynthesis, were likely to provide a suitable condition for carbonate precipitation on the twigs.

• Economic and Environmental Geology
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• v.56 no.3
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• pp.217-227
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• 2023

Crystalline calcium carbonate (CaCO₃) occurs in various geological and aqueous environments as calcite, aragonite, and vaterite. These minerals also have practical applications in engineered settings. Synthetic methods of calcium carbonate have been developed for scientific research and technical applications. For example, these methods have become widely adopted for studying the formation of CaCO₃ minerals and (geo-)chemical processes involving these minerals in natural and engineered systems. Furthermore, these methods have the potential to be applied in various technical and biomedical fields. Water-based synthesis is particularly important for simulating the formation of calcium carbonate minerals in natural aqueous environments. This review paper describes the procedures and experimental conditions for water-based synthetic methods of each calcium carbonate polymorph, compares the morphological and structural features of the resulting crystals, and analyzes the crystallization mechanisms.

• Journal of Korean Society of Water and Wastewater
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• v.11 no.1
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• pp.53-63
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• 1997

The corrosion problems in water distribution system are reduced by decreasing the agressivity of drinking water which is evaluated by marble test and saturation indices(LSI or CCPP etc.). Marble test is a reliable method to determine the actual saturation condition of treated water. This study was done to determined the aggressivity of tap water and the effectiveness of $Ca(OH)_2$ and NaOH dosage for corrosion control. The drinking water in Seoul were evaluated by marble test and Langelier Index(LSI) and Calcium Carbonate Precipitation Potential(CCPP). The results indicated that the drinking water in Seoul were undersaturated as Calcium Carbonate($CaCO_3$). The LSI and CCPP of the water treated with $Ca(OH)_2$ were higher than that of water treated with NaOH. Therefore, to increase the Alkalinity and Calcium Hardness for corrosion control in water distribution system, $Ca(OH)_2$ is more effective than NaOH.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.31 no.1
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• pp.16-23
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• 2021

Lithium carbonate recovered from the waste solution generated during the lithium secondary battery manufacturing process contains heavy metals such as cobalt, nickel, and manganese. In this study, the recrystallization of lithium carbonate was performed to remove heavy metals contained in the powder and to increase the purity of lithium carbonate. First, the leaching efficiency of lithium carbonate according to pH in the aqueous hydrochloric acid solution was examined, and the effect on the recrystallization of lithium carbonate according to the equivalent and concentration of sodium carbonate was confirmed. As the equivalent and concentration of sodium carbonate increased, the recovery rate of lithium carbonate improved. And the SEM image showed that the crystal shape was changed depending on the reaction conditions with sodium carbonate. Finally, the high purity lithium carbonate of 99.9% or more was recovered by washing with water.

• Resources Recycling
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• v.27 no.5
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• pp.23-29
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• 2018

Generally $NiSO_4$ and $NiCl_2$ were used as raw materials for producing nickel carbonate. In the case of the produced nickel carbonate, $Na_2SO_4$ and NaCl are generated on the surface and inside of the nickel carbonate to decrease the purity of the nickel carbonate. High purity nickel carbonate can be produced according to the degree of removal of such impurities. In this study, $NiCl_2$ produced by nickel MHP solvent extraction process was used to study the production of nickel carbonate. High purity nickel carbonate was prepared by the conditions according to the nickel salt and carbonate equivalence ratio, the reduction of Na and Cl in nickel carbonate according to the washing of nickel carbonate, and the reduction of Na and Cl according to the washing water temperature.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2005.04a
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• pp.405-407
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• 2005

To evaluate the main hydrogeochemical characteristics, river waters are investigated using element리 and isotopic compositions in South Korea. In this area, the chemical compositions are mostly classified into three groups; $Ca^{2+}-{HCO_3}^-$ type, $Ca^{2+}-Cl^{-}-{NO_3}^-$ type and $Ca^{2+}-{HCO_3}^{-}-Cl^{-}-{NO_3}^-$ type. These types are affected by two major factors: water-rock interaction and anthropogenic inputs such as sewage and fertilizers. Based on the values of ${\delta}^{18}O$ and ${\delta}D$, most of waters are originated from precipitation except two samples contaminated. The lithology and geography of basins mainly control the water chemistry. Elemental and isotopic compositions show that water chemistry are mainly controlled by three end members, especially by carbonate dissolution, and suggest that anthropogenic input affect the water chemistry. Also, three weathering sources are identified: silicates, dolomite and limestone.

• Journal of Environmental Science International
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• v.1 no.2
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• pp.71-79
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• 1992

Selective extraction procedure has been used to quantify copper and cadmium In association with the various phases of aquatic sediment such as exchangeable/adsorbed, carbonate, manganese oxides, organic matter and iron oxides. Changes of pH influenced on the partitioning of copper in carbonate and exchangeable/ad- sorbed phases and of cadmium in carbonate phase of aquatic sediment. Addition of NTA and EDTA, copper and cadmium associated with carbonate phase were released from sediment to water. Total partitioning coefficient was 8.361 for copper and 0.497 for cadmium. The relative binding strengths of copper and cadmium to each solid phase can be ranked by using the partitioning coefficints. For copper it was observed that carbonate > organic matter > exchangeable/adsorbed > manganese oxides > iron oxides and for cadmiunm it was observed that exchangeable/adsorbed > carbonate > manganese oxides > organic matter > iron oxides.

• Journal of the Korean Society for Marine Environment & Energy
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• v.19 no.1
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• pp.18-24
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• 2016

Mineral carbonation is a technology for permanently storing carbon dioxide by reacting with metal oxides containing calcium and magnesium. In this study, we used sea water and alkaline industrial by-product such as paper sludge ash (PSA) for the storage of carbon dioxide through direct carbonation. We found the optimum conditions of both sea water content (mixing ratio of sea water and PSA) and reaction time required in the direct carbonation through various experiments using sea water and PSA. In addition, we compared the amounts of carbon dioxide storage with the cases when sea water and ultra-pure water were separately used as solvents in the direct carbonation with PSA. The amount of carbon dioxide storage was calculated by using both solid weight increase through the carbonation reaction and the contents of carbonate salts from thermal gravimetric analysis. PSA particle used in this study contained 67.2% of calcium. The optimum sea water content and reaction time in the carbonation reaction using sea water and PSA were 5 mL/g and 2 hours, respectively, under the conditions of 0.05 L/min flow rate of carbon dioxide injected at $25^{\circ}C$ and 1 atm. The amounts of carbon dioxide stored when sea water and ultra-pure water were separately used as solvents in the direct carbonation with PSA were 113 and $101kg\;CO_2/(ton\;PSA)$, respectively. The solid obtained through the carbonation reaction using sea water and PSA was composed of mainly calcium carbonate in the form of calcite and a small amount of magnesium carbonate. The solid obtained by using ultra-pure water, also, was found to be carbonate salt in the form of calcite.

• The Journal of Natural Sciences
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• v.4
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• pp.95-102
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• 1991

The influences of various concentrations of thallium carbonate on the hydration of tricalcium silicate which is widely used to the inorganic materials have been studied using an isothermal microcalorime-ter. The experimental results indicate that the hydration of tricalcium silicate is accelerated in the presence of thallium carbonate, namely the concentration of thallium carbonate is increased, the rate of hydration is also increased. The x-ray diffraction analysis shows that the concentration of tricalcium silicate decreases rapidly in the presence of thallium carbonate. Differential thermal analysis of tricalcium silicate hydrated in the persence of thallium carbonate indicates the presence of calcium carbonate. The nonevaporable water content and the degree of hydration of tricalcium silicate show that the accelerating action of thallium carbonate is more pronounced only during the early period of hydration. Analytical results of the liquid phase in contact with the tricalcium silicate paste indicate that the concentrations of calcium and hydroxyl ions are changed considerably in the presence of thallium carbonate.