• Journal of Food Hygiene and Safety
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• v.17 no.4
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• pp.183-187
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• 2002

This study was performed to investigate the utility of egg-shell calcium with calcium soak egg-shell in the vinegar. We compared examination eluted quantity with ionization rate in each condition. The results were as follows. 1 The degree of elution and ionization of calcium was proportional to the amount of vinegar and added acetic acid in the vinegar for elution. And ionization rate was the most high in case of 200 ml vinegar volume. 2. fluted quantity were increased in the rank order to 4$0^{\circ}C$ > 3$0^{\circ}C$ > 2$0^{\circ}C$ by temperature but the rank order of ionization of calcium was 3$0^{\circ}C$ > 2$0^{\circ}C$ > 4$0^{\circ}C$ by temperature. The occurrence of unacceptable flavor resulting from the immersion at 4$0^{\circ}C$ was another obstacle to adopt. 3. Eluted quantity and ionization rate of the egg-shell calcium were appeared excellent in case of the brewage vinegar at ventilation condition. The case of brown rice vinegar did not show a considerable difference, but eluted quantity and ionization rate were appeared the most excellent to the other sample. 4. The optimum condition for elution and ionization of the egg-shell calcium was appeared Immersing egg-shells in the brewed rice-bran vinegar at 3$0^{\circ}C$ for three days.

• Proceedings of the KAIS Fall Conference
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• 2008.11a
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• pp.459-462
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• 2008

본 논문에서는 $10K_2O$-30CaO-$60P_2O_5$ mol%를 기본조성으로 하여 Fe, Cu, Zn의 미량성분을 첨가하여 유리를 제조하고 용출 특성을 평가 하였다. 제조된 유리는 미량성분의 첨가량에 따라 유리의 투명도가 변하는 것이 관찰되었다. 용출특성은 측정 4시간 뒤 pH값 증가되는 것으로 16시간 후 pH가 증가하는 것으로 관찰되었다. 여기서 pH의 증가는 염기성산화물이 용출되는 것으로, 감소는 $P_2O_5$구조인 망목형성구조가 붕괴되어지면서 산성이온이 용출되어지는 것으로 판단되어진다. ICP관찰시에는 함량이 증가하면서 K, Ca, P이온의 용출량이 감소되었고, Zn, Cu, Fe이온의 용출량이 증가하는 경향이 관찰되었다.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.11 no.2
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• pp.604-607
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• 2010

The glass formation and the dissolution property in $P_2O_5-K_2O$-FeO-CuO system were studied. In the batch process, the content of P2O5 was fixed at 60mol% and the other elements were varied from 10~40mol%. The prepared glasses were soaked in the D.I. water up to 13hr and the dissolution properties were investigated with the solutions sampled every 2 hr. The result shows that the $P_2O_5$ was leached out firstly from Phosphate glass system and then Cu and Fe ions were observed according to atmosphere change in solution. ICP shows that the dissolution amount in Phosphate was depended on the glass structure and the highest dissolution amount of CuO and FeO ions was observed when the 10mol% $K_2O$ was added in batch process.

• Economic and Environmental Geology
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• v.43 no.6
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• pp.573-587
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• 2010

Bioleaching experiments were effectively carried out at $42^{\circ}C$, $52^{\circ}C$ and $62^{\circ}C$ to leach the more valuable metal ions from sphalerite using bacteria. The pH values of the bioleaching solution were constantly maintained for 10 days in the range of 2.40 to 2.55. In these bioleaching experiments, rod-shaped bacteria attached to the sphalerite surface were continuously observed in the sample. Along with the increase in the leaching temperatures, the concentration of Zn and Pb increased in the control sample of leachates, whereas the concentration of Fe increased in the sample containing bacteria. At $42^{\circ}C$, $52^{\circ}C$ and $62^{\circ}C$ the biological leaching content of Zn was found to be 9.5, 2.8 and 2.9 times higher than that in the chemical leaching content, respectively. At these temperatures, the content of Pb in the bacterial sample of the leachate was detected to be 14.8, 7.4 and 3.8 times higher than that of the control sample of the leachate, respectively.

• Applied Chemistry for Engineering
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• v.9 no.4
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• pp.574-578
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• 1998

Electrochemical Ion Exchang(EIX) electrode containing Amberlite IRP-64 as a cation ion exchange resin and Stylene-Buthylene-Rubber(SBR) as a binder was fabricated by the compressed diecasting method. The adsorption and elution characteristics in copper sulfate solution were investigated at the various electrode potentials and electrolyte pHs. In the adsorption process, it was found that the maximum adsorption rate of copper was obtained at -1800 mV and the ratio of adsorption was 92% during 90 min. In the elution process, the elution rate of copper was increased in proportion to anodic potential in the present experimental range and the ratio of elution was 88% during 50 mins at 3600 mV. The adsorption and elution processes were significantly affected by the variation of local pH in the vicinity of electrochemical ion exchange electrode. The higher performances of adsorption and elution were elution were obtained at basic and acidic eletrolytes.

• Korean Journal of Mineralogy and Petrology
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• v.36 no.1
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• pp.33-40
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• 2023

Todorokite is a manganese oxide mineral containing Mg²⁺ in a tunnel structure in which MnO₆ octahedra share corners. In order to investigate the suitability and efficiency of high temperature-treated todorokite as a material for adsorption and fixation of Cs, Cs was ion exchanged and the amount of leached Cs from todorokite was measured. The todorokite used in this study was synthesized by transforming Na-birnessite to Mg-buserite and used as a precursor. After high temperature treatment, Cs exchanged todorokite changed to birnessite and hausmannite as the temperature increased. The amount of leached Cs was investigated for Cs exchanged todorokite which was reacted with distilled water and 1 M NaCl solution at different reaction times. In general, for the samples reacted with 1 M NaCl solution, the fixation of Cs was quite effective, although the amount of leached Cs was greater due to the ion exchange reaction with Na. As the treatment temperature increased, the amount of leached Cs increased and then decreased again, which was related to the mineral phases formed at each temperature. As birnessite was formed, the amount of leached Cs increased, but as birnessite decreased, that decreased again. As the mineral phase changed to hausemanite, the amount of Cs decreased rapidly. The results of our study show that Cs exchanged todorokite can be used as a material that effectively fixes Cs and prevents its diffusion by high temperature treatment.

• Journal of the Mineralogical Society of Korea
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• v.23 no.3
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• pp.251-265
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• 2010

A column bioleaching experiment at room temperature with no addition of sulfuric acid was effectively carried out to leach the valuable elements from pyrite, which is common mine waste. The Fe concentration of pyrite leachate from bioleaching column was 14 times higher than that of the control leachate, and secondary minerals were not formed. The $SO_4^{2-}$ concentration of the pyrite leachate was 2.99 times higher. The XRD intensity of the (111), (200), (220), (311), (222), (230) and (321) planes of pyrite decreased, whereas the intensity of (210) and (211) increased after column bioleaching.

• Resources Recycling
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• v.21 no.5
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• pp.88-92
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• 2012

We tried to measure the fixed quantity of $Ni^{2+}$ion among the metals which were eluted by distilled water from the Fly Ash Leach Liquor(FALL) with a spectrophotometric method. In addition, we researched absorbance values which had different contained quantity of $V^{3+}$ion in contrast with $Ni^{2+}$ion ppm to find out the influence of the $V^{3+}$ion existed in the FALL on the spectrophotometric fixed quantity of $Ni^{2+}$ion. As a result, when $V^{3+}$ ion has below 50% of amount of $Ni^{2+}$ion, the fixed quantity of $Ni^{2+}$ion among the FALL was able to be confirmed by spectrophotometry.

• Journal of the Korea Concrete Institute
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• v.23 no.5
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• pp.647-656
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• 2011

In radioactive waste repositories constructed in underground, concrete member could be in contact with groundwater for a long time. However, this pure water creates concentration gradients which lead to the diffusion of Ca ions from the pore water and the degradation of underground concrete. Therefore, this study is aimed at investigating the alteration of pore structure and loss of compressive strength associated with dissolution. The results showed that as the leaching period became longer, the pore volume within 50 nm to 500 nm in diameter is greatly increased. Also, the volume of pores larger than 200 nm rapidly increased during initial leaching time and those below 200 nm gradually increased. Furthermore, the compressive strength gradually decreased with increase of degraded thickness. The residual strength of the degraded concrete with OPC was in the range of 33% to 58%.

• Korean Journal of Mineralogy and Petrology
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• v.36 no.4
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• pp.313-321
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• 2023

Numerous studies have investigated the adsorptive sequestration of radioactive cesium in the natural environment. Among these studies, adsorption onto minerals and high-temperature treatment stand out as highly effective, as demonstrated by the use of zeolite. In this study, cesium was ion-exchanged with birnessite and subsequently underwent high-temperature treatment up to 1100℃ to investigate both mineral phase transformation and the leaching characteristics of cesium. Birnessite has a layered structure consisting of MnO₆ octahedrons that share edges, demonstrating excellent cation adsorption capacity. The high-temperature treatment of cesium-ion-exchanged birnessite resulted in changes in the mineral phase, progressing from cryptomelane, bixbyite, birnessite to hausmannite as the temperature increased. This differs from the phase transformation observed in the tunneled manganese oxide mineral todorokite ion-exchanged with cesium, which shows phase transformation only to birnessite and hausmannite. The leaching of cesium from cesium-ion-exchanged birnessite was estimated by varying the reaction time using both distilled water and a 1 M NaCl solution. The leaching quantity changed according to the treatment temperature, reaction time, and type of reaction solution. Specifically, the cesium leaching was higher in the sample reacted with 1 M NaCl compared to the sample with distilled water and also increased with longer reaction time. For the samples reacted with distilled water, the cesium leaching initially increased and then decreased, while in the NaCl solution, the leaching decreased, increased again, and finally nearly stopped like the sample in the distilled water for the sample treated at 1100℃. These changes in leaching are closely associated with the mineral phases formed at different temperatures. The phase transformation to cryptomelane and birnessite enhanced cesium leaching, whereas bixbyite and hausmannite hindered leaching. Notably, hausmannite, the most stable phase occurring at the highest temperature, demonstrated the greatest ability to inhibit cesium leaching. This results strongly suggest that high-temperature treatment of cesium-ion-exchanged birnessite effectively immobilizes and sequesters cesium.