• 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.

• Journal of Advanced Marine Engineering and Technology
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• 제28권2호
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• pp.300-308
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• 2004

The formation mechanism of anodic oxide films on Mg alloys when anodized in NaOH solution. was investigated by focusing on the effects of anodizing potential. Al content. and anodizing time. Pure Mg and Mg-Al alloys were anodized for 10 min at various potentials in NaOH solutions. $Mg(OH)_2$ was generated by an active dissolution reaction at the surface. and the product was affected by temperature. The intensity ratio of $Mg(OH)_2$ in the XRD analysis decreased with increasing applied potential. while that of MgO increased. The anti-corrosion properties of anodized specimens at each constant potential were better than those of non-anodized specimens. The specimen anodized at an applied potential of 3 V had the best anti-corrosion property. And the intensity ratio of $Mg_{17}Al_{12}$/Mg increased with aluminum content in Mg-Al alloys. During anodizing. the active dissolution reaction occurred preferentially in ${\beta}\;phase(Mg_{17}Al_{12})$ until about 4 mins. and then the current density increased radually until 7 mins. The dissolution reaction progressed in a phase(Mg) which not formed the intermetallic compound. which had a lower Al content. In the anodic polarization test of $0.017\;mol{\cdot}dm^-3$ NaCl and $0.1\;mol{\cdot}dm^-3\;Na_2SO_4$ at 298 K. the current density of Mg-15 mass% Al alloy anodized for 10 mins increased. since the anodic film that forms on the a phase is a non-compacted film. The anodic film on the phase for 30 mins was a compact film as compared with that for 10 mins.

• Journal of Electrochemical Science and Technology
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• 제14권1호
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• pp.59-65
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• 2023

Sodium hydroxide solutions are often employed as sterilization agents in the pharmaceutical industry. Here, the chloride content is considered as a critical impurity. In this study, an electrochemical method was developed to remove chloride ions (Cl^-) through the oxidative deposition of AgCl on a Ag anode. The Cl^- content in the commercially available 50% w/w NaOH solution employed was approximately 100 mg Cl^-/kg NaOH. As the OH^- content is approximately 18,000 times higher than the Cl^- content, the formation of AgCl may be expected to be thermodynamically less favorable than the formation of Ag₂O. However, activation energies for AgCl and Ag₂O formation have been reported to be approximately 3.8 and 31.2 kJ/mol, respectively, and indicate that AgCl formation is favored. AgCl can be selectively produced by controlling the anode potential. Here, the Cl^- concentration was reduced to less than 50 mg Cl^-/kg NaOH when an anode potential of 0.18 or 0.19 V vs. Hg/HgO (reference electrode) was applied for one hour at 50℃. XRD analysis and visual monitoring of the Ag anode confirmed the oxidative deposition of AgCl on the anode surface as well as the electrochemical desalination of the concentrated NaOH solution.

• Corrosion Science and Technology
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• 제22권5호
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• pp.387-392
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• 2023

The objective of this study was to evaluate corrosion resistance of Zn-Al-Mg alloy coated steel in residential water with trace quantities of Cl^-. Comparative evaluations were performed using two commercial coated steel products, GI and Galvalume, as reference samples. Examination of corrosion morphology and measurement of weight loss revealed that the Zn-Al-Mg alloy coated steel exhibited higher corrosion resistance than reference samples. This finding suggests that the alloy coated steel possesses long-term corrosion resistance not only in highly Cl^- concentrated environments such as seawater, but also in environments with extremely low levels of Cl^- found in residential water. The primary factor contributing to the superior corrosion resistance of the Zn-Al-Mg alloy coated steel in residential water is the formation of an inhibiting corrosion product composed primarily of two phases: Zn₅(OH)₆(CO₃)₂ and Zn₅(OH)₈Cl₂·H₂O. The preferential dissolution of Mg from the corroded coating layer can increase alkalinity, which might enhance the thermodynamical stability of Zn₅(OH)₆(CO₃)₂.

• 한국표면공학회지
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• 제37권5호
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• pp.253-262
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• 2004

Calcareous deposits are the consequence of pH increase of the electrolyte adjacent to metal surface affected by cathodic current in seawater. It obviously has several advantages over conventional coatings, since the calcareous deposit coating is formed from coating (Mg$^{2+}$, $Ca^{2+}$) naturally existing in seawater. In consideration of this respect, environment friendly calcareous deposit films were formed by an electro deposition technique on steel substrates submerged in 48$^{\circ}C$ natural seawater. And the influence of current density, coating time and attachment of steel mesh on composition ratio, structure and morphology of the electrodeposited films were investigated by Scanning Electron Microscopy(SEM), Energy Dispersive Spectroscopy(EDS) and X-Ray Diffractor(XRD), respectively. Accordingly, this study provides a better understanding of the composition between the growth of $Mg(OH)_2$ and $CaCO_3$ during the formation of electro deposit films on steel substrate under cathodically electrodeposition in $48^{\circ}C$ natural seawater. The Mg compositions, in general, are getting decreased regardless of current density but Ca compositions are getting increased as electrodeposition time runs. That is, $Mg(OH)_2$ compounds of brucite structure shaped as flat type is formed at the initial stage of electrodeposition, but CaCO$_3$ compounds of aragonite structure shaped as flower type is formed in large scale. Besides, $Mg(OH)_2$ compounds were much formed at 5 A/$\m^2$ environment condition compared to the 3 A/$\m^2$ and 4 A/$\m^2$ environment conditions. This is because that OH- which was comparatively largely generated at the metal surface is preferably combined with $Mg^{2+}$TEX>.

• Corrosion Science and Technology
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• 제22권2호
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• pp.123-130
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• 2023

This study aimed to evaluate corrosion resistance of steel coated with GI and Zn-Al-Mg alloy using cyclic corrosion test (CCT) with electrochemical polarization and impedance measurements. Results showed that the Zn-Al-Mg alloy coated steel had a much higher corrosion rate than GI coated steel in early stages of corrosion. With prolonged immersion, however, the corrosion rate of the Zn-Al-Mg alloy coated steel greatly decreased, mainly owing to a significant decrease in the cathodic reduction reaction and an increase in polarization resistance at the surface. This was closely associated with the formation of protective corrosion products including Zn₅(OH)₈Cl₂·H₂O and Zn₆Al₂(OH)₁₆CO₃. Moreover, when the steel substrate was locally exposed due to mechanical damage, the kinetics of anodic dissolution from the coating layer and the formation of protective corrosion products on the surface of the Zn-Al-Mg alloy coated steel became much faster compared to the case of GI coated steel. This could provide a longer-lasting corrosion inhibition function for Zn-Al-Mg alloy coated steel used in plant farms.

• Korean Chemical Engineering Research
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• 제57권5호
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• pp.714-722
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• 2019

산 염기성질이 다양하게 존재하는 담체($SiO_2-Y_2O_3$, $Al_2O_3$, $SiO_2-ZrO_2$, $SiO_2$, $TiO_2$, MgO) 상에 17 wt% Ni을 고정한 상태에서 함침법을 사용하여 촉매를 제조하여 수소 존재 하에 에탄올과 암모니아의 환원성 아민화 반응에 대한 촉매활성을 비교 평가하였다. 반응 전후에 있어 사용된 촉매는 X-선 회절, 질소 흡착, 에탄올-승온탈착(EtOH-TPD), 이소프로판올-승온탈착(IPA-TPD), 수소 화학흡착을 사용하여 특성분석을 수행하였다. pH 9.5 이상에서 침전법을 사용하여 $ZrO_2$와 $Y_2O_3$ 담체 제조 시 파이렉스 반응기에서 미량의 Si 용융으로 인해 $SiO_2-ZrO_2$와 $SiO_2-Y_2O_3$ 복합 산화물이 각각 생성되었다. 사용된 촉매 중에서 $Ni/SiO_2-Y_2O_3$ 촉매가 가장 좋은 활성을 보였으며 이는 높은 니켈 분산도와 EtOH-TPD와 IPA-TPD에서의 낮은 탈착온도 등과 밀접한 관련이 있었다. Ni/MgO 촉매상에서의 낮은 촉매 활성은 NiO-MgO 고형물 형성에 기인한 것으로 보이며, $Ni/TiO_2$ 경우에서는 담체-금속 간의 강한 상호 작용으로 인해 낮은 니켈 금속 상 존재로 인해 반응성이 낮게 나왔다. $TiO_2$와 MgO 이외의 담체를 사용한 경우에 있어서 유사한 에탄올 전환율에서의 에틸아민류와 아세토니트릴 선택도는 큰 차이를 보이지 않았다.

• 자원환경지질
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• 제30권4호
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• pp.327-340
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• 1997

Geochemical characteristics of groundwater, based on chemical analyses of 54 water samples, differ among main rocks of Haman formation, Panyawoel formation, andesite and granite in Daegu area in relation to mineralogical and chemical compositions of the rocks. Concentrations of most solutes are higher in groundwaters of Haman and Panyawoel formations than in those of andesite and granite. High concentrations of $Ca^{2+}$ and $Mg^{2+}$ in groundwaters of the sedimentary rocks result mainly from reaction of $CO_2$-charged water with calcite and weathered feldspars. Average groundwaters in the sedimentary rocks are oversaturated with respect to calcite. Major types of groundwaters are hard $Ca(HCO_3)_2$ and $CaSO_2-CaCl_2$ with hardness of 442 mg/l for Haman formation and 275 mg/l for Panyawoel formation whereas they are soft $Ca(HCO_3)_2$ with hardness 35 mg/I for andesite and 39 mg/I for granite. $Ca(HCO_3)_2$ type results mainly from calcite-dissolution and $CaSO_4-CaCl_2$ from pyrite and partly from domestic pollutants. $CaSO_4-CaCl_2$ type may indicate that groundwaters in the sedimentary rocks are more evolved geochemically than those in the igneous rocks, but it is not obvious because the type might be affected by pyrie dissolution and domestic pollutions. Acid rain is buffered by active calcite in the sedimentary rocks. In the igneous rocks acid rain might react with gibbsite and other forms of $Al(OH)_3$ that might have accumulated as weathering products of primary silicates, and is buffered.

• 한국세라믹학회지
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• 제40권3호
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• pp.234-240
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• 2003

보통 포틀랜드 시멘트에 CSA계 팽창재를 l0 wt% 혼합한 시멘트 경화체를 MgS $O_4$. 7$H_2O$ l0 wt%로 제조된 용액에 침지시켜 물성을 측정하였다. 재령의 경과에 따라서 압축강도, 수화생성물 및 미세구조변화를 관찰한 결과 천연원료로 제조된 CSA계 팽창재［No. 6(C/(equation omitted) : 2.29, A/(equation omitted) : 0.16)]는 초기에 미세한 에트링자이트 생성 및 후기에는 $\beta$-C$_2$S의 수화 반응으로 경화체가 치밀화되어 OPC 보다 $Mg^{2＋}$, S $O_4$$^{2－}$ 이온의 확산에 대한 저항성이 증가되었다.

• 공업화학
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• 제20권2호
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• pp.234-240
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• 2009

마그네슘염과 알칼리를 출발물질로 하는 수산화마그네슘 제조에서 공정 변수가 생성되는 입자의 크기, 형상 및 응집도에 미치는 영향에 대해 완전 요인배치(full factorial) 실험계획법(Design of experiment)으로 연구하였다. 수열합성에서는 알칼리/$MgCl_2$ 몰 비가 낮을수록, $MgCl_2$ 농도와 수열처리 온도가 높을수록 평균입경은 커지고 1차 입자 크기와 2차 입자 크기가 유사하지만, 침전법으로 제조한 수산화마그네슘은 1차 입자의 응집현상으로 2차 입경은 커지며, 응집성은 알칼리원의 종류와 $MgCl_2$의 농도에 따라 달라졌다. 알칼리원의 종류에 따른 차이는 $NH_4OH$를 사용한 경우 NaOH를 사용한 것보다 입자의 크기가 커지고 분산성이 우수하였다. 크기 및 표면 상태가 다른 샘플을 선정하여 LDPE와 EVA 혼합수지에 혼합하여 난연 특성을 비교하였을 때, 50, 55% 함량에서는 일반적으로 2차 입경 크기가 감소함에 따라 LOI값은 상승하지만, UL-94에서는 1차 입자가 작은 경우에 더 우수한 등급을 받는 경우가 있었다. 60%의 높은 함량에서 입자의 제조경로와 무관하게 UL-94는 V0 등급이지만, 미립이더라도 응집성있는 경우 한계산소지수가 상대적으로 낮다는 것을 알 수 있었다.