• Journal of the Mineralogical Society of Korea
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• v.31 no.3
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• pp.173-182
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• 2018

The precipitation and phase transformation processes of iron minerals in acid mine drainage have a great influence on the behavior of trace elements in drainage. However, it is not easy to accurately trace these processes in natural environments, and therefore, most studies have carried out in the laboratory to obtain the information on the precipitation and transformation of those minerals. In this study, the precipitation of minerals and the changes of trace elements in drainage water were investigated at different pH values in actual acid mine drainage collected from the Dalsung mine. The amount of some precipitated minerals was not enough for the mineral identification. However, from the minerals identified, amorphous minerals were formed first, and then goethite was precipitated probably from schwertmannite. When the pH of the sample was high (10), amorphous phases of minerals were still observed at even high pH (pH 10). With increasing time, the pH values decreased by precipitation and transformation of minerals. All the elements showed low concentrations at high pH (8, 10), which might be due to the precipitation of minerals at high pH and the effect of surface charge, and the concentrations of elements gradually increased with time. In the case of sulfur, it also increased in water due to the transformation of schwertmannite to goethite.

• Resources Recycling
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• v.29 no.5
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• pp.48-54
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• 2020

Sulphuric acid (H₂SO₄) leaching and hydrolysis were experimented for the recovery of titanum dioxide (TiO₂) from the water-leached residue followed by soda-roasting spent SCR catalysts. Sulphuric acid leaching of Ti was carried out with leachate concentration (4~8 M) and the others were fixed (temp.: 70 ℃, leaching time: 3 hrs, slurry density: 100 g/L, stirring speed: 500 rpm). For recovering of Ti from the leaching solution, hydrolysis precipitation was conducted at 100 ℃ for 2 hours in various mixing ratio (leached solution:distilled water) of 1:9 to 5:5. The maximum leachability was reached to 95.2 % in 6 M H₂SO₄ leachate. on the other hand, the leachability of Si decreased dramatically 91.7 to 3.0 % with an increase of H₂SO₄ concentration. Hydrolysis precipitation of Ti was proceeded with leaching solution of 8 M H₂SO₄ with the lowest content of Si. The yield of precipitation increased proportionally with a dilution ratio of leaching solution. Moreover, it increased generally by adding 0.2 g TiO₂ as a precipitation seed to the diluted leaching solution. Ultimately, 99.8 % of TiO₂ can be recovered with the purity of 99.46 % from the 1:9 diluted solution.

• Journal of Korean Society for Atmospheric Environment
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• v.22 no.1
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• pp.15-24
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• 2006

Precipitation samples were collected at Anmyeon (1997 - 2004), Uljin, and Gosan (1998 ~ 2004), the background area of the Korean Peninsula. These samples were analyzed for the concentration of 9 major ionic components ($F^{-}$,$Cl^{-}$, $NO_{3}^{-}$, $SO_{4}^{2-}$, $Na^{+}$, $NH_{4}^{+}$, $K^{+}$, $Mg^{2+}$, $Ca^{2+}$) with including a pH and an electric conductivity. Data quality for these samples was verified by ion balance and conductivity balance which are based on GAW manual for precipitation chemistry and the number of valid data at Anmyeon, Uljin, and Gosan is 249, 173, and 188, respectively. During the study period, the precipitation-weighted average pH at Anmyeon, Uljin, and Gosan was found to be 4.81, 4.87 and 4.89, respectively and each annual average pH was showed below pH 5.6 for every site. From the frequency survey on the precipitation acidity, the occurrence rate of acid rain below pH 5.6 is greater than $80\%$ for every site. Particularly, the highest occurrence rate for strong acid rain below pH 4.5 was found at Anmyeon, $32.1\%$, compared with other sites ($10.4\%$ at Uljin, $15.4\%$ at Gosan). That's because acidifying species (nss-$SO_{4}^{2-}$, $NO_{3}^{-}$) are remarkably high concentration at Anmyeon.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2003.09a
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• pp.310-313
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• 2003

The precipitation of heavy metals within the region of pH jump is inevitable in the conventional electrokinetic remediation technology. This study prevents the interest species from precipitating through the injection of flushing solutions in which HCl, acetic acid, citric acid, EDTA and SDS dissolved. The cumulative flow resulted from electroosmosis appear in order of Citric acid

• Proceedings of the Korea Water Resources Association Conference
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• 1992.07a
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• pp.325-328
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• 1992

The purpose of this research is to develop the technique of heavy metal removal from wastewater. The research is divided into two parts, one part uses complex precipitation and the other uses adsorption. In the first part of the study, humic acid is used as the complex agent, humic acid is a polyelectrolyte with a high complexation affinity. Lead, copper, zinc and cadmium were studied for their complex precipitation efficiencies. In the batch studies, humic acid was effective in removing 100% of the lead and 48.2% of the copper respectively from wastewater without anytreatment. The efficiency of cadmium and zinc, however, was very low. In the second part of the study, wastewater is introduced at the top of a silicagel adsorption column and then bottom effluent concentration is analyzed. The results of the analysis are used to draw a breakthrough curve.

• Preventive Nutrition and Food Science
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• v.7 no.1
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• pp.43-47
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• 2002

Crude caseinomacropeptide (CMP) was prepared from Na-caseinate using a commercial renneting enzyme. Most of the crude CMP was released from the Na-caseinate by hydrolyzing with the enzyme for 40 min. The hydrolysis of the k-casein with carbohydrate was slower than that of the k-casein without carbohydrate, as shown by the analyses of the sialic acid content and the tricine-SDS-polyacrylamide gel electrophoresis. The yield of crude CMP from Na-caseinate was 3.7%. Cation exchange chromatography showed that the crude CMP consisted of 40.5% CMP and 59.5% caseinogylcomacropetide (CGP). The effect of the TCA concentration on the solubility of CMP and CGP was determined by using crude CMP. The amounts of crude CMP and sialic acid decreased in the proportion to the increase of trichloroacetic acid (TCA) concentration from 2 to 12%, suggesting that the CGP containing carbohydrate, as well as the CMP having no carbohydrate, was precipitated in a range of 4 to 12%, depending on the TCA concentration. This result supports the hypothesis that the different non-glycosylated and glycosylated forms of CMP have different sensitivities to TCA precipitation.

• Proceedings of the Korea Air Pollution Research Association Conference
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• 1995.10a
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• pp.99-102
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• 1995

• Spatial Information Research
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• v.3 no.1
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• pp.29-38
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• 1995

• Journal of the Korean Ceramic Society
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• v.29 no.12
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• pp.963-969
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• 1992

This paper describes the feasibility for a direct production of zinc oxalate powders from zinc-loaded D2EHPA solutions combining the purification and the precipitation in one operation unit. This process has the potential as an alternative to conventional method for the synthesis of zinc oxide precursor particles from the hydrometal-lurgical processes. Zinc was extracted into D2EHPA in kerosene and then zinc-loaded D2EHPA solution was emulsified with oxalic acid-HCl solution to precipitate zinc oxalate powder, which was readily calcined to zinc oxide. The precipitation kinetics and yield were sensitive to experimental conditions. The morphology, size and size distribution of the zinc oxalate powders varied with zinc/oxalate ion riatio, temperature, and the presence of SPAN 60, which affected nucleation, growth, and the emulsion characteristics.

• Korean Journal of Environmental Biology
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• v.23 no.4
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• pp.374-378
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• 2005

A diffusion - precipitation method was developed to determine acid volatile sulfide (AVS) concentrations in freshwater sediments. This method uses silver nitrate as a sulfide trap solution and the concentration of trapped sulfide is determined gravimetrically. The proposed diffusion - precipitation method is more rapid and less expensive than previously developed purge- and - trap methods. Spiked sodium sulfide recoveries using this method $(97\~120\%)$ were similar with a previously developed diffusion - absorption method $(93.8\~115\%)$ and about $20\%$ greater than a previously developed purge-and-trap method $(74.6\~105\%)$. Detection limit of this method $(0.1\;{\mu}mole\;S\;g^{-l})$ was comparable with that of diffusion-absorption method $(0.06\;{\mu}mole\;S\;g^{-l})$ and purge-and-trap method $(0.05\~0.5\;{\mu}mole\;S\;g^{-l})$.