• Korean Journal of Soil Science and Fertilizer
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• v.36 no.3
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• pp.105-112
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• 2003

Effects of magnesium sulfate ($MgSO_4$) and magnesium hydroxide $[Mg(OH)_2]$, which have different chemical characteristics, on soil pH, electrical conductivity (EC), and exchangeable cation distributions were investigated. Using plastic columns packed with a loam soil, the two Mg-fertilizers were treated at the rate of $300kg\;MgO\;ha^{-1}$ and water was applied on the soil surface four times at every 7 days. Soil samples were taken at 5, 10, 15, and 20 cm depth after 7 days of each water application. Magnesium hydroxide could increase soil pH, but due to the low solubility of $Mg(OH)_2$, the effect on pH was limited on the surface soil. Soil pH was lowered in the $MgSO_4$ treatment and the effect was found through the 20 cm depth. Since the pH decrease in $MgSO_4$ treated soil was due to the salts from $MgSO_4$, after leaching of most salts from the investigated soil depth pH was not significantly different from that of non-treated soil. Soil EC was increased in $MgSO_4$ treatment through the soil depth, but in $Mg(OH)_2$ treatment EC was slightly increased only at the surface layer. Exchangeable Mg was increased in both of the treatments at surface layer after the first water application. In $Mg(OH)_2$ treatment, the increase of exchangeable Mg was found only at 5 cm depth through the experiment, but leaching down of Mg in the $MgSO_4$ treatment was very apparent. High concentration of Mg in the $MgSO_4$ treated soil could effectively replace exchangeable Ca through the investigated soil depth, but the effect of $Mg(OH)_2$ on exchangeable Ca was not significant.

• Journal of the Korean Society for Advanced Composite Structures
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• v.6 no.2
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• pp.63-69
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• 2015

It has been well known that concrete structures exposed to chloride and sulfate attack environments lead to significant deterioration in their durability due to chloride ion and sulfate ion attack. The purpose of this experimental research is to evaluate the resistance against chloride ion and sulfate attack of the cementless concrete replacing the cement with ground granulated blast furnace slag. For this purpose, the cementless concrete specimens were made for water-binder ratios of 40%, 45%, and 50%, respectively and then this specimens were cured in the water of $20{\pm}3^{\circ}C$ and immersed in fresh water, 10% sodium sulfate solution for 28 and 91 days, respectively. To evaluate the resistance to chloride ion and sulfate attack for the cementless concrete specimens, the diffusion coefficient for chloride ion and compressive strength ratio, mass change ratio, and length change ratio were measured according to the NT BUILD 492 and JSTM C 7401, respectively. It was observed from the test results that the resistance against chloride ion and sulfate attack of the cemetntless concrete were comparatively largely increased than those of OPC concrete with decreasing water-binder ratio.

• KSBB Journal
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• v.21 no.6 s.101
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• pp.428-432
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• 2006

This study investigated the effect of sulfate source on removal efficiency in electrokinetic bioremediation which needs sulfate to degrade contaminants by an applied microorganism. The representative contaminant and the applied microorganism were phenanthrene and Sphingomonas sp. 3Y, respectively. When magnesium sulfate was used, the magnesium ion combined with hydroxyl ion electrically-generated at cathode to cause the decrease of electrolyte pH, and then the microbial activity was inhibited by that. When ammonium sulfate and disodium sulfate were used to solve the pH control problem, the pH values of electrolyte and soil solution were maintained neutrally, and also the high microbial activity was observed. With the former sulfate source, however, ammonium retarded the phenanthrene degradation, and so the removal efficiency decreased to 12.0% rather than 21.8% with magnesium sulfate. On the other hand, the latter improved the removal efficiency to 27.2%. This difference of removal efficiency would be outstanding for an elongated treatment period.

• Resources Recycling
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• v.31 no.1
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• pp.21-28
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• 2022

The smelting reduction of spent lithium-ion batteries results in metallic alloys of cobalt, nickel, and copper. To develop a process to separate the metallic alloys, leaching of the metallic mixtures of these three metals with H₂SO₄ solution containing 3% H₂O₂ dissolved all the cobalt and nickel, together with 9.6% of the copper. Cyanex 301 selectively extracted Cu(II) from the leaching solution, and copper ions were completely stripped with 30% aqua regia. Selective extraction of Co(II) from a Cu(II)-free raffinate was possible using the ionic liquid ALi-SCN. Three-stage cross-current stripping of the loaded ALi-SCN by a 15% NH₃ solution resulted in the complete stripping of Co(II). A process was proposed to separate the three metal ions from the sulfuric acid leaching solutions of metallic mixtures by employing solvent extraction.

• Korean Journal of Agricultural and Forest Meteorology
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• v.2 no.4
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• pp.190-197
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• 2000

Anions such as C $l^{[-10]}$ , N $O_3$$^{[-10]}$ , S $O_4$$^{2-}$, P $O_4$$^{3-}$, and organic anions, that do not become a part of the clay mineral crystal lattice, are of considerable interest in soils which are a potential sink caused by acid rain. In this paper, elution of native sulfate and breakthrough curves (BTC) were obtained from miscible displacement of non-specifically or specifically adsorbed anions through non-saturated or saturated Bt soil of Chungwon series. The shape and position of the BTC's could be affected by adsoprtion and ion exchange onto the soil particle surfaces. Measured BTC's for oxalic acid under unsaturated and saturated conditions showed that less pore volumes were required to displace the native S $O_4$$^{2-}$S from the soil column, and that maximum detection limit of oxalic acid reached earlier than under unsaturated. The retarded BTC's to the righthand side could be attributed by different adsorption behavior of each anion, although BTC's may be influenced by the smaller order of velocity change. The alternate breakthrough and elution curves show the rapid approach to the maximum detection limit of C/Co = 1, compared to progressive tailing of elution curve to reach to C/Co = 0. The probable explanation for asymmetric elution patterns for both anion is that the anion was selectively adsorbed on the positively charged soil surface from the solution passing in the soil column. On the other hand, the variations of pH in effluent showed that pH was increased to 7 in the first 6 pore volume and then gradually decreased to pH 4.

• Resources Recycling
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• v.25 no.2
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• pp.3-9
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• 2016

Separation of Zr(IV) and Hf(IV) from sulfuric acid solutions was investigated by extraction with several acidic extractants such as Versatic acid, LIX 63, and Cyanex 301. From strong sulfuric acid solutions, the separation of Zr(IV) and Hf(IV) by Versatic acid and LIX 63 was not possible, while selective extraction of Hf(IV) over Zr(IV) was obtained with Cyanex 301. However, the extraction percentage of the two metals was much lower compared to that by D2EHPA. Mixing of TBP with Cyanex 301 and D2EHPA led to negative effect on the extraction and separation of the two metal ions. The difference in the extraction reaction and separation selectivity between HCl, $HNO_3$ and $H_2SO_4$ media with each extractant was discussed.

• Journal of the Korean Geotechnical Society
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• v.17 no.4
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• pp.145-151
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• 2001

본 연구에서는 울산 삼산지역의 도시 개발로 인하여 다량 발생되고 있는 건설잔토의 유효이용을 목적으로 대상토에 생석회와 화학 첨가제를 혼합하여 안정처리를 할 경우 보조기층 및 노상용 재료로써의 사용 가능성을 평가하였다. 1가 이온($Na^{+}$, $K^{+}$)가 2가 이온(Ca$^{2+}$, $Mg^{2+}$), 염화물(Cl)과 황산염(So$_4$)으로 구성된 화학 첨가제의 첨가에 따른 일축압축강도를 비교한 결과, 1가 이온의 첨가시 장기강도 발현이 우수한 것으로 나타났고, 염화물(Cl)은 첨가시 강도 발현이 우수한 것으로 나타났다. 건설잔토에 생석회와 CaCl$_2$를 첨가하면, 생석회로 처리된 시료에 비해 2배~4배의 강도가 증가되어 생석회 안정화에 대한 효과가 좋은 것으로 나타났다. 원시료토에 생석회, 생석회와 화학 첨가제로 안정처리하여 도로의 보조기층재료나 노상용 재료로의 사용여부를 평가한 결과, 생석회와 CaCl$_2$로 안정처리한 경우만이 시방기준 CBR 10%이상, 소성지수 10%이하를 만족시켜 노상용 재료로서의 사용가능성을 확인할 수 있었다.

• Journal of Environmental Science International
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• v.12 no.9
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• pp.1011-1016
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• 2003

Adsorption of phosphate, sulfate, and copper ion to goethite was investigated. Goethite was prepared in the alkaline solution. In the single adsorbate systems, the final equilibrium plateau reached within 20 min. The adsorption isotherms of the individual ions could be well described by the Langmuir equation. The maximum adsorption capacities (q$\_$max/) were calculated as 0.483 m㏖/g and 0.239 m㏖/g at pH 3 for phosphate and sulfate ion, and 0.117 m㏖/g at pH 6 for copper ion, respectively, In competitive adsorption system with phosphate and sulfate, phosphate ion was a stronger competitor for adsorption on goethite than sulfate ion, which was consistent with higher affinity of phosphate ion for the surface compared to sulfate ion. The existence of sulfate ion enhanced the adsorption of copper ion but the adsorption of sulfate was inhibited when copper ion was present.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.13 no.3
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• pp.103-108
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• 1980

The contents of inorganic conservative constituents in Nagdong River water were determined at Mulgeum where the intake station for Busan city water is located. Samples were taken at intervals of one hour from 7 a.m. to 7 p.m. at spring and neap tides of every month from January 1979 to April 1980. Annual ranges and means of the chemical constituents were as follows: electrical conductivity $99-912\mu\mho/cm,\;200\mu\mho/cm;$ chlorides 6.0-256 ppm, 17.2 ppm; sulfates 4.1-37.9 ppm, 23.5 ppm; calcium 4.2-28 ppm, 13 ppm; magnesium 2.2-23 ppm, 5.6 ppm; sodium 5,0-126 ppm, 14 ppm; and potassium 1.2-10.8 ppm, 2.6 ppm respectively. At several times in this period, the concentrations of chloride ion exceeded 150 ppm that is the criteria for drinking water. The chloride ion concentration was higher at spring tides than that at neap tides and the contents of inorganic conservative constituents were higher in winter than those in summer. The chloride ion concentration showed the highest value at Mulgeum about 4 hors after the high water in Busan harbour.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2004.11a
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• pp.481-484
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• 2004

다중 채널 전극 위에 세포를 성장시켜 전극면을 통해 검출되는 신경 신호의 손실을 줄이고 주파수의 변형을 줄이기 위해서 전극과 전해질의 사이의 impedance를 줄이는 것이 바람직하다. 전하 이동을 증대시키기 위해서는 낮은 impedance가 요구되며 이를 위한 전극의 개선 방안으로 전극면이 증착될 기판의 표면을 거칠게 하여 결과적으로 전극면의 표면적을 넓히는 방법을 모색하였다. 기판으로 사용되는 glass(Pyrex#7740)의 구성 물질 중에서 4%를 차지하는 $N^+$ 이온을 황산 용액으로 표면 처리하여 제거함으로써 매끈한 표면을 거칠게 하여 표면적을 넓힐 수 있다. 기판으로 사용되는 glass (pyrex#7740) $1cm{\times}1cm{\times}0.05cm$를 50%, 95% 농도의 황산 용액 내에서 각각 30분, 60분 동안 상온에서 표면처리를 진행하였다. AFM을 이용하여 표면을 관찰한 결과 황산 용액 95%에서 30분간 표면 처리를 진행한 시편에서 최대 $4000{\AA}$정도의 조도를 얻었다. 이후 동일 시편에 대해 전극으로 사용될 Ti/Au를 각각 $500{\AA}/2500{\AA}$ 증착 후 사진식각 공정으로 MEA(Multi-channel electrode array)를 제작하여 impedance를 측정한 결과, 표면 처리 후 impedance가 70% 개선되었음을 측정하였다.