• 한국환경농학회지
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• 제20권5호
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• pp.352-357
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• 2001

Cadmium (Cd) has been identified as a potential contaminant in agricultural and environmental soils. Ionic condition in the soils is an important factor to influence Cd availability. In this study, the effect of sulfate or nitrate application on Cd sorption in acidic and calcareous soils was investigated. The Cd, sulfate $(SO_4)$, and nitrate $(NO_3)$ sources were solutions of $CdCl_2$, $K_2SO_4$, and $KNO_3$, respectively. The soil-solution system pH was affected by the application of sulfate or nitrate in both acidic and calcareous soil system, but there was not clear pH difference between pre- and simultaneous applications of sulfate or nitrate (PAS/PAN or SAS/SAN). Solution ionic strength (I) values were similar between the acid and calcareous soil systems after applying the Cd even though it was significantly different in the untreated control soils. However after applying the sulfate or nitrate, the I values increased and were always higher with SAS/SAN treatments. Solution Cd concentration also increased with the application of sulfate or nitrate. However, the Cd concentration in soil solution controlled by Cd sorption in the systems was different between PAS/PAN and SAS/SAN treatments only in the calcareous soil system, but not in the acidic soil system. The difference in Cd concentration between SAS/SAN and PAS/PAN in the calcareous systems may be caused by system pH, ionic strength, complexation, and predominately, competition of the $Cd^{2-}$ with the index $K^+$ ion. Potassium ion-Cd competition in the acidic soil system may be minimized because of the abundance of hydrogen ions.

• 한국세라믹학회지
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• 제34권8호
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• pp.861-869
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• 1997

In order to investigate the reaction in the system of anhydrite II-blast furnace slag, the paste hydration which made up with a liquid/solid ratio of 0.45 for 1, 3, 7, 14, 28days by the addition of accelerators to 10~30wt.% slag with natural gypsum calcined for 1hour at 500/$700^{\circ}C$ was studied by combined water determination, XRD, DTA, DSC and SEM. As a result of this experiment, it was found that hydration rate was faster in the system calcined at 50$0^{\circ}C$. Therefore the anhydrite was converted to calcium sulfate dihydrate in the hydration for 1day but the slag was not almost reacted. For the gypsum calcined at $700^{\circ}C$, the hydraton rate in the system of K2SO4 addition was faster than others in the earier period, but the activated effect of the system of Al2(SO4)3 addition was regarded as the highest over 3days. As the amount of slag was increased, they dydration rate was delayed and ettringite was observed in the case of K2SO4 system. However both Al2(SO4)3 and AlK(SO4)2 systems showed calcium sulfate dhydrate only as hydrated products.

• 한국세라믹학회지
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• 제44권9호
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• pp.465-470
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• 2007

This paper presents an experimental study of the sulfate resistance of mortars and pastes exposed to sodium sulfate solutions up to one year. In order to check deterioration modes due to sulfate attack, the sodium sulfate solution was varied at three concentration steps (3,380, 10,140 and 33,800 ppm of $SO_4^{2-}$ ions), and maintained at ambient temperature. The tests include a visual examination, expansion and compressive strength loss measurements as well as x-ray diffraction tests. The experimental data indicated that the use of cement with a low $C_3A$ content and low silicate ratio has a beneficial effect on the sulfate attack of mortars. In contrast, the mortars with a high $C_3A$ content and high silicate ratio became severely degraded due to the formation of ettringite, gypsum and/or thaumasite in the cement matrix.

• 신재생에너지
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• 제19권1호
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• pp.1-11
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• 2023

A large amount of carbon monoxide (CO) is generated in circulating fluidized bed combustion, the process whereby a hot cyclone separates unburned fuel. However, calcium sulfate (CaSO₄), when combined with a high CO content, can cause fouling on the surface of the steam tube installed inside the integrated recycle heat exchangers (INTREX). In this study, CaSO₄ decomposition was investigated using 0.2-3.2 vol.% CO and 1-3 vol.% oxygen (O₂) at 850℃ for 20 min in a lab-scale fluidized bed reactor. The results show that CaSO₄ decomposes into CaS and CaO when CO gas is supplied, and SO₂ emissions increase from 135 ppm to 1021 ppm with increasing CO concentration. However, the O₂ supply delayed SO₂ emissions because the reaction between CO and O₂ is faster than that of CaSO₄; nevertheless, when supplied with CaCO₃, the intermediate product, SO₂ was significantly released, regardless of the CO and O₂ supply. In addition, agglomerated solids and yellow sulfur power were observed after solid recovery, and the reactor distributor was corroded. Consequently, a sufficient O₂ supply is important and can prevent fouling formation on the INTREX surface by suppressing CaSO₄ degradation.

• 한국분말재료학회지
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• 제27권5호
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• pp.401-405
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• 2020

Magnesium hydroxide sulfate hydrate (MHSH) whiskers were synthesized via a hydrothermal reaction by using MgO as the reactant as well as the acid solution. The effects of the H₂SO₄ amount and reaction time at the same temperature were studied. In general, MHSH whiskers were prepared using MgSO₄ in aqueous ammonia. In this work, to reduce the formation of impurities and increase the purity of MHSH, we employed a synthesis technique that did not require the addition of a basic solution. Furthermore, the pH value, which was controlled by the H₂SO₄ amount, acted as an important factor for the formation of high-purity MHSH. MgO was used as the raw material because it easily reacts in water and forms Mg⁺ and MgOH⁺ ions that bind with SO₄^2- ions to produce MHSH. Their morphologies and structures were determined using X-ray diffraction (XRD) and scanning electron microscopy (SEM).

• 한국결정성장학회지
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• 제27권4호
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• pp.173-177
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• 2017

PNS 감수제와 시멘트 페이스트의 유동성의 관계를 평가하기 위해 물시멘트비 35 %에 PNS의 감수제 첨가하여 세 가지 시멘트에 대해 평가하였다. 세 가지 시멘트의 화학적 성질은 XRD, XRF로 평가하고, 물시멘트비 33 %인 콘크리트에 대한 $Na_2SO_4$의 첨가 효과는 압축강도, 슬럼프, 공기 함량의 측정에 의해 평가하였다. 실험 결과는 시멘트 A 및 C에 황산나트륨 2.6 %를 첨가하면 슬럼프 손실이 개선됨을 보여 주었으며, 시멘트 E의 경우 황산나트륨 1.3 % 첨가가 효과적이었다.

• Journal of Chest Surgery
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• 제11권3호
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• pp.368-372
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• 1978

Ribostamycin sulfate is a new aminoglycoside antibiotic which is effective against organisms resistant to other conventional antibiotics, Particularly E. coli, and Staphylococcus group. Our clinical studies were performed on 20 patients who were admitted to Thoracic Surgical Dept of National Medical Center from May '77 to September '77, and the following results were obtained; 1. Among 20 patients, 13 were excellently improved and 4 responded moderataly, but 3 patients were not improved. So, 85% of the patients were controlled with Ribostamycin sulfate administration. 2. The rate of effectiveness of Ribostamycin sulfate was 85.7% against E. coli, 92.3% against Staphylococcus, and 75% against klebsiella, revealing 83.3% in average. 3. No side effects were observed. 4. From our clinical studies, Ribostamycin sulfate is expected to possess in high therapeutic value in surgical infectins caused by both gram positive and negative microorganisms.

• 한국세라믹학회지
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• 제50권3호
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• pp.201-205
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• 2013

Magnesium hydroxide sulfate hydrate ($5Mg(OH)_2.MgSO_4{\cdot}3H_2O$, abbreviated 513 MHSH) whiskers were synthesized using MgO and $MgSO_4.7H_2O$ as reactants without addition of basic solution. Previously, MHSH whiskers were prepared by hydrothermal method using $MgSO_4$ in aqueous ammonia. In this work, for the first time, we synthesized a high purity MHSH via ambient pressure. In addition, a high molar ratio of $MgSO_4$ : MgO is an important key to the formation of high purity MHSH. Also, it was possible to prepare whiskers with high aspect ratio using an increasing reaction time in the reaction between the remaining $SO_4^{2-}$ ions and the ${Mg(OH)_6}^{4-}$ fragment, finally producing one-dimensional whiskers.

• 수도
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• 통권4호
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• pp.50-56
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• 1975

• 한국표면공학회지
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• 제5권3호
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• pp.77-85
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• 1972

A method of preparation of synthetic ignorgaic coating on copper (patina) has been presented . An Eh--pH diagram was constructed for the present Cu-H2O-SO$_4$ system using the most recently available thermodynamic data. In the path of the patination at room temperature the general behaviour of copper in acidic copper sulfate solutions with potassium chlorate as an oxidizing agent appeared to follow those predictable in this Eh-pH diagram. In the presence 0.05 molar cupric sulfate at a temperature of about 28$^{\circ}C$ a green brochantite (CuSO$_4$$.$3Cu(OH)$_2$) layer was formed on copper sheet in 20 days. In a solution having an initial pH of 3.5 the development of a brochantite coating has been observed to take place in two stages. In the first, a layer of cuprous oxide formed on the copper at a relatively rapid rate. In the ensuing step the outer layer of cuptrite was oxidized at much slower rate to form brochantite. The syntetic coatings appeared to consist of crystal-lites of brochanitite growing perpendicular to the cuprose oxide surface. The outer tips of the -crystallites were reasily broken off and gave to the layer a rather chalky character. Underneath, at the brochantite Cu$_2$O interface, however, the green layers were firmely attached. The effect of reagent concentration , solution agitation , and moderate temperature increase were investigated to improve the quality of coating. So also in a qualitative way were the effect of light.