• Journal of the Korean institute of surface engineering
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• v.51 no.5
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• pp.325-331
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• 2018

Calcium carbonate($CaCO_3$) films were formed by an eco-friendly electro-chemical technique on steel substrates in synthesized distilled water solutions containing $NaHCO_3$, $CaCl_2$ and $MgCl_2$ with different ratio respectively. It was investigated to confirm the effect of $Mg^{2+}$ concentration by Scanning Electron Microscopy(SEM), Energy Dispersive x-ray Spectroscopy(EDS) and X-Ray Diffraction(XRD) respectively. From an experimental result, only calcite crystals were found in solution containing no $Mg^{2+}$. By increasing concentration of $Mg^{2+}$, deposition rate decreased and crystal structure was transformed form calcite to aragonite. In case of including $MgCl_2$ 300mM in synthesized solutions containing $NaHCO_3$, $CaCl_2$ 60mM, it was showed over the 90% of aragonite contents which have quite high deposition rate of aragonite. Also, it was confirmed that $Mg^{2+}$ acted as inhibitor on the films which made transforming from calcite to aragonite.

• Economic and Environmental Geology
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• v.49 no.5
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• pp.335-347
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• 2016

The mineralogical and geochemical characteristics of diverse carbonate rocks can be investigated by using VNIRSWIR(visible near infrared-short wavelength infrared) spectroscopic analysis as a rapid, nondestructive, and inexpensive tool. Comparing whole rock analysis to VNIR-SWIR spectroscopic analysis, the analytical method was investigated to estimate CaO contents, mud impurity, and whiteness of carbonate rocks involved in high-grade limestones in the field. We classify typical carbonate rocks in the upper Pungchon Formation in high-grade limestone mine area such as the Gangweon, Chungmu and Baegun mine in the Jeongseon area. The results show that powdered specimen has much higher reflectance than cutted specimen between the same sample. Whiteness is highly correlated with reflectance(0.99) for powdered specimen. The absorption of mineral mixtures shifts in position as a result of the mass ratio of calcite and dolomite in the Chungmu mine by changing to 75:25, 50:50, and 25:75. The absorption peak position in carbonate mixtures is highly correlated with CaO contents(0.98~0.99). Based on color system, the carbonate rocks are grouped into (milky) white, light grey, light brown, grey, and dark grey. The absorption peak position shifts from 2340 nm to 2320 nm as CaO contents decrease from 55.86 wt.% to 29.71 wt.%. We confirmed that absorption peak position shifts depending on the amount of Ca, which is bonded to $CO{_3}^{-2}$, Mg, and Fe contents replacing Ca. This result suggests that CaO contents in carbonate rocks can be considered to quantitative analysis in the field by spectroscopic analysis.

• Journal of Soil and Groundwater Environment
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• v.7 no.2
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• pp.45-52
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• 2002

Water chemistry in the Munkyeong hot-spring expresses high values of EC(1,857 $mutextrm{s}$/cm), $HCO_3$(1,250 mg/l), $SO_4$(147.60 mg/l), Mg(43.05 mg/l), and Ca(279.43 mg/l). The precipitates of small quantity is formed in lower temperature, but much of in case apply heat by boiler. Although mineral that is settled from original ground water is most calcite, aragonite and calcite at the same time crystallized in boiler. The $CO_3$ is present predominantly as $HCO_3^{-}$ and $H_2$$CO_3$, $SO_4$, Mg and Ca are present as free ion. Ca is saturated with respect to carbonate such as aragonite and calcite but slightly undersaturated with respect to anhydrite and gypsum Al is saturated with diaspore and gibbsite. The precitptates are composed of carbonate such as calcite and aragonite and amorphous Fe-hydroxide.

• Journal of Soil and Groundwater Environment
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• v.18 no.5
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• pp.1-6
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• 2013

This study was performed to develop a method for quantitative analysis obtaining the amount of calcium carbonate minerals formed when Ca salts biomimetically reacted with carbon dioxide. There were two methods compared; 1) volumetric calcimeter method that determining the amount of released carbon dioxide after calcium carbonate minerals were acidified by 4N HCl and 2) Thermogravimetry-Differential Thermal Analysis (TG-DTA) adopting differential decomposition temperature breaking-up the structural link within calcium carbonate minerals. The comparisons were made by batch experiment (i.e., biocalcification process) along with control (i.e., nominal concentration of $CaCO_3$ prepared). For the control, TG-DTA took a minor root mean square deviation (RMSD) of 1.1~5.9 mg, whereas volumetric calcimeter exposed a greater RMSD of 28.3 mg. For the biocalcification, the amount of $CaCO_3$ was more precisely obtained for TG-DTA rather than that of volumetric calcimeter. It was decided that TG-DTA was more successfully used for quantitative analysis to observe the amount of calcium carbonate minerals derived from biocalcification.

• Korean Journal of Mineralogy and Petrology
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• v.36 no.3
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• pp.167-183
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• 2023

The Janggun Pb-Zn deposit consists of Mn orebody, Pb-Zn orebody and Fe orebody. The Mn orebody composed of manganese carbonate orebody and manganese oxide orebody on the basis of their mineralogy and genesis. The geology of this deposit consists of Precambrian Weonnam formation, Yulri group, Paleozoic Jangsan formation, Dueumri formation, Janggum limestone formation, Dongsugok formation, Jaesan formation and Mesozoic Dongwhachi formation and Chungyang granite. This manganese carbonate orebody is hydrothermal replacement orebody formed by reaction of lead and zinc-bearing hydrothermal fluid and Paleozoic Janggum limestone formation. The wallrock alteration that is remarkably recognized with Pb-Zn mineralization at this hydrothermal replacement orebody consists of mainly rhodochrositization with minor of dolomitization, pyritization, sericitization and chloritization. Carbonates formed during wallrock alteration on the basis of paragenetic sequence are as followed : Ca-dolomite (Co type, wallrock) → ankerite and Ferroan ankerite (C1 type, early stage) → ankerite (C2 type) → sideroplesite (C3 type) → sideroplesite and pistomesite (C4 type, late stage). This means that Fe and Mn elements were enriched during evolution of hydrothermal fluid. Therefore, The substitution of elements during wallrock alteration beween dolomitic marble (Mg, Ca) and lead and zinc-bearing hydrothermal fluid (Fe, Mn) with paragenetic sequence is as followed : 1)Fe ↔ Mn and Mn ↔ Mg, Ca, Fe elements substitution (ankerite and Ferroan ankerite, C1 type, early stage), 2)Fe ↔ Mn, Mn ↔ Mg, Ca and Mg ↔ Ca elements substitution (ankerite, C2 type), 3)Fe ↔ Mn, Fe ↔ Ca and Mn ↔ Mg, Ca elements substitution (sideroplesite, C3 type), and 4)Fe ↔ Mg, Fe ↔ Mn and Mn ↔ Mg, Ca elements substitution (sideroplesite and pistomesite, C4 type, late stage)

• Korean Journal of Soil Science and Fertilizer
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• v.38 no.6
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• pp.334-339
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• 2005

Although phosphogypsum can have profound effects on both the physical and chemical properties of certain soils with supplying the essential elements, no widespread use of by-product phosphogypsum will be made unless such uses pose no threat to the public health and soil contaminations. This study was conducted to evaluate the effects of phosphogypsum on the growth of oriental melon and soil properties in plastic film house. Phosphogypsum was treated at the rate of $70kg\;CaO\;10a^{-1}$ and the effects were compared with the treatment of Ca-Mg carbonate. In the treatment of phosphogypsum, early growth of oriental melon was significantly increased comparing to the growth in the Ca-Mg carbonate treatment. Total fruit yield was not different between the treatments of phosphogypsum and Ca-Mg carbonate, but marketable fruit yield was higher in the phosphogypsum treatment. Although Ca and S contents in oriental melon were increased in the phosphogypsum treatment, contents of toxic heavy metals including As, Cd, Cr, Cu, and Pb were not different between the two treatments. Also, soil pH and contents of extractable toxic metals in the soil were not significantly different between the two treatments after the experiment. These results suggest that phosphogypsum can be a valuable substitute for lime materials in high pH soils of plastic film house.

• Journal of the Korean Ceramic Society
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• v.41 no.12 s.271
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• pp.889-892
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• 2004

Acicular type aragonite precipitated calcium carbonate was synthesized by carbonation reaction of $Ca(OH)_2$ slurry and $CO_2$ gas. As increasing the initial concentration of $Mg^{2+}$ ion, calcite crystal phase substantially decreased while that of aragonite crystal phase increased. According to XRD and EDS analysis, it was found that the addition of $MgCl_2$ induced the $Mg^{2+}$ ion to substitute in $Ca^{2+}$ ion site of calcite lattice then the unstabled calcite structure be resolved, consequently the growth of calcite structure is interrupted while the growth of aragonite structure is expedited.

• Economic and Environmental Geology
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• v.41 no.1
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• pp.47-56
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• 2008

pH and Eh were measured at 25 points in the abandoned Dalcheon mine. And, major ion components $(Na^+,\;K^+,\;Ca^{2+},\;Mg^{2+},\;Cl^-,\;SO_4^{2-},\;CO_3^{2-},\;HCO_3^-)$ were analyzed through groundwater sampling at 41 points. pH and Eh were measured the highest concentration in serpentinite area. And, pH was between weak alkaline and intermediate values in study area. Groundwater in study area was dominated oxidation-reduction environment caused by reaction with carbonate rock. Because sulfur components contained in carbonate, serpentinite, arsenopyrite and pyrite was dissolved by groundwater, $SO_4^{2-}$ component was high in study area. And $Ca^{2+},\;Mg^{2+}$ of cations were high. Correlation coefficients of ion components in tailing dumps were 0.95 between $Ca^{2+}\;and\;SO_4^{2-}$, 0.86 between $Ca^{2+}\;and\;Mg^{2+}$, 0.85 between $Mg^{2+}\;and\;SO_4^{2-}$. Correlation coefficients of ion components in bedrock were 0.86 between $Mg^{2+}\;and\;SO_4^{2-}$, 0.68 between $Ca^{2+}\;and\;SO_4^{2-}$. Concentration range of $Ca^{2+}$ in tailing dumps was $6.85{\sim}323.58mg/L,\;and\;3.18{\sim}207.20mg/L$ in bedrock. Concentration range of $SO_4^{2-}$ in tailing dumps was $21.54{\sim}1673.17mg/L,\;and\;2.04{\sim}1024.64mg/L$ in bedrock. By the result of Piper diagram analysis with aquifer material, groundwater in tailing dumps was $Ca-SO_4$ type. Groundwater quality types with bedrock material were Mg-$SO_4$ and Mg-$HCO_3$ types in serpentinite area, Ca-$HCO_3$ type in carbonate area, Na-K and $CO_3+HCO_3$ types in hornfels, respectively. As a result of this study, groundwater in tailing dumps were dissolved $Ca^{2+},\;Mg^{2+}\;and\;SO_4^{2-}$ components with high concentration. Also, these ion components were transported into bedrock aquifer.

• Korean Journal of Soil Science and Fertilizer
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• v.24 no.1
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• pp.35-40
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• 1991

A laboratory column experiment was conducted to learn the desalinization effect of rice straw, fresh or predecayed in limed marine soil, compared with gypsum. One third of Ca equivalent to indigenous Na plus Mg of the soil was applied to the top 10g out of 80g of total column soil, mixing one half of it to the top soil and the rest spreading on the surface. 1. Pre-decaying of rice straw in limed marine soil promoted the permeability of column soil. but showed a less effectiveness in desalinization of sodium than lime alone or lime plus fresh rice straw treatemenents. 2. Gypsum and calcium carbonate treatments without rice straw fixed Mg in the limed top soil and washed it down disolving more from the layer immediatly be low the treated top soil But the treatment of calcium carbonate and rice straw both together washed out Mg more from lower layers than the upper's, showing only physical desalinization. 3. The desalinization of Na was also severe in the layer immediately below the $CaSO_4$ treated top soil, leauing more Na ilo the top soil, which seemed to be attributed to the peptisation of the top soil and retard peptisation of desalinization when washed the soil applying not enough amount or non of gypsum.

• Journal of Soil and Groundwater Environment
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• v.19 no.2
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• pp.7-15
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• 2014

This study was conducted to understand the chemical characteristics of groundwater in carbonate areas of Korea. In this study, data on pH, electric conductivity (EC), $Ca^{2+}$, $Mg^{2+}$, $Na^+$, $K^+$, $Cl^-$, $SO_4{^{2-}}$, and $HCO_3{^-}$ were collected from 97 wells which were installed in various carbonate rock regions of Korea. The pH values ranged from 5.7 to 9.9, and the average value was 7.3. The concentration range showed differences between the maximum value of $HCO_3{^-}$ and the medium to minimum values of $Ca^{2+}$, $Mg^{2+}$, $Na^+$, $Cl^-$, $SO_4{^{2-}}$, and $K^+$ in the study area. The average value of EC was $374{\mu}S/cm$, higher than in granite and gneiss areas, where the value is $176{\mu}S/cm$. Most of the groundwater was type $Ca-HCO_3$, and some was type $Mg-HCO_3$. The relationship between $Ca^{2+}$, $Cl^-$, and $HCO_3{^-}$, respectively, and EC showed relatively significant positive correlations compared to the other dissolved components. However, the determination coefficients for $Mg^{2+}$, $Na^+$, $SO_4{^{2-}}$, and $K^+$ were very low less than 0.2. These results indicate that the source of $Ca^{2+}$ and $Mg^{2+}$ is relatively simple (carbonate dissolution) compared to other sources. The sources of $Na^+$, $K^+$, $Cl^-$, $SO_4{^{2-}}$, and $HCO_3{^-}$ might be not only water-rock interactions, but also irrigation return flow, because many groundwater wells had been developed for irrigation purposes. Subsequently, the influence of agriculture on groundwater chemistry was evaluated using a cumulative plot of $SO_4{^{2-}}$. The threshold value of $SO_4{^{2-}}$ calculated from the cumulative frequency curve was 29.2 mg/L. Therefore, 12.4% of all the groundwater wells were affected by agricultural activity.