• 한국표면공학회:학술대회논문집
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• 한국표면공학회 2015년도 추계학술대회 논문집
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• pp.268-268
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• 2015

The corrosion protection behavior of AZ31 magnesium alloy (Mg alloy) with cathodic electrophoretic coating (E-coating) pretreated by cerium-based conversion coatings at various pH was investigated in this study. Cerium-based conversion coatings (CeCCs) were deposited on AZ31 Mg alloy by immersion treatment in the nitrate-based cerium salt solution. The morphology and composition of the CeCCs were analyzed using scanning electron microscopy and energy dispersive X-ray spectroscopy. The corrosion properties of the AZ31 Mg alloy pretreated with cerium coating and subsequently E-coated were studied during salt-spray testing. The surface morphologies of the E-coated Mg alloy were examined in detail after different testing times using digital photography. It was found that the protective properties of the E-coating on AZ31 Mg alloy generated are heavily dependent upon the CeCC factors such as treatment time, coating thickness and pH of the solution.

• Bulletin of the Korean Chemical Society
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• 제30권12호
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• pp.3057-3060
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• 2009

Ionic palladium(II) complex, [($Me_4en)Pd(L)]_2(ClO_4)_4\;(Me_4$en = N,N,N',N'-tetramethylethylenediamine; L = bis-(4-(4-pyridylcarboxyl)phenyl)methane), allows to form a monodisperse submicrosphere without any template or additive. Surface-perchlorates on the submicrosphere have been exchanged by anionic pH indicators such as thymol blue, bromothymol blue, and bromocresol green. The ionic and amphiphilic properties of the palladium(II) complex appear to be primarily associated with the formation and easy surface-anion exchange of submicrosphere. The surface-anion exchange through the electrostatic interaction is a very good tool for the surface-modification. The color of the pH indicator-exchanged submicrospheres is very sensitive to pH and Hg$^{2+}$ cation, and thus they are promising to submicrospherical indicators.

• 한국세라믹학회지
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• 제37권7호
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• pp.721-725
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• 2000

In this study, the dispersion stability of nano-sized CeO2 particles, synthesized by hydrothermal method in aqueous was evaluated from observing the surface potential behavior of CeO2 particle synthesized by solid state reaction. The isoelectric point(IEP) of nano-sized CeO2 synthesized by hydrothermal synthesis was found to be pH 9 contrary to the isoelectric point of micro-sized CeO2 synthesized by solid state reaction at pH 6.7. IEP was shifted to pH 2.0 as the addition of D-3019 from 0.1 to 1.0 wt%. The surface potential of CeO2 particles synthesized by hydrothermal synthesis was reduced as the addition of B-1001 used as a binder without change of IEP because the absorption of B-1001 polymer on the CeO2 particles shifted the shear plane of CeO2 particles outward away from the surface. This surface potential behavior was well correlated with the dispersion stability of slurry.

• 한국결정성장학회지
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• 제16권3호
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• pp.127-131
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• 2006

세라믹소지에 발생하는 온도별 백화생성기구를 백화를 형성하는 양이온과 음이온을 분석하여 규명하였다. 백화가 발생된 세라믹 소지의 표면을 SEM과 EDS 분석을 하여 백화의 주 성분은 Ca와 S임을 확인하였다. 세라믹소지를 pH 7과 pH 10에서 각기 습식혼합 하였으며, 이때 여과된 액을 ICP와 IC 분석을 하여, 양이온 및 음이온 농도분석을 하였다. pH 7에서 제조된 세라믹 소지의 Ca 이온농도는 pH 10에서 제조된 세라믹소지의 Ca 이온농도의 8배 값을 보였으며, pH 10에서 제조된 세라믹소지는 $1100^{\circ}C$ 이상으로 소결된 소지에서도 백화가 발견되지 않았다.

• 한국수소및신에너지학회논문집
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• 제6권2호
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• pp.91-100
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• 1995

To investigate the surface state of $Mg_2Ni$ which was exposed to the air, a chemical treatment was undertaken with $H_2SO_4$ solution. During chemical treatment, the change of pH was measured continuously and the chemically treated specimen was hydrided to study the effect of chemical treatment on the hydrogenation. The pH changing behavior with the various $H_2SO_4$ concentration appeared very diffemrently. Especially in the solution including 3CC $H_2SO_4$, the behavior of pH change can be divided 3 steps. It is also shown that the $Mg_2Ni$ chemically treated with $H_2SO_4$ can be hydrided even under room temperature. By the SEM observation the was reasion that after chemical treatment the surface of a particle was covered with Ni layer.

• 대한화학회지
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• 제64권2호
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• pp.74-78
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• 2020

산성 영역에서 작동하는 고감도 형광 pH 센서막을 제조하기 위하여 실란화된 유리 표면 상에 push-pull 공액 염료(DCMP)를 공유결합에 의해 고정화하였다. DCMP 유도체(DCMA), 2-hydroxyethyl methacrylate (HEMA)및 triethylene glycol dimethacrylate의 혼합물을 광개시 공중합하여 pH 감응성 형광센서막을 제조하였다. 분광학적 측정 결과, pH 2.0-5.0 사이에서 pH가 증가함에 따라 센서막의 흡광도가 증가하였으며, 같은 pH 범위에서 pH 증가에 따라 센서막의 형광 세기도 약 50배 정도 증가하였다. 산성 조건에서 pH 변화에 대한 센서막의 감응은 가역적이고 재현성이 우수하였다. 또한 센서막은 20-50초 사이의 비교적 짧은 감응 시간과 여러 금속이온 존재에서 수소 이온에 대해 높은 선택성을 나타내었다.

• Carbon letters
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• 제7권1호
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• pp.1-8
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• 2006

The activated carbon "C" was obtained by carbonization followed by activation with steam at 40% of burn-off. Oxidized carbons C-N, C-P and C-H were obtained by oxidizing the activated carbon C with concentrated nitric acid, ammonium peroxysulfate and hydrogen peroxide, respectively. The textural properties of the carbons were determined from nitrogen adsorption at 77 K. The acidic surface functional groups were determined by pH titration, base neutralization capacity and electrophoretic mobility measurements. The cation exchange capacities of un-oxidized and oxidized carbons were determined by the removal of Cu(II) and Ni(II) from their aqueous solutions. The surface area and the total pore volume decreased but the pore radius increased by the treatment of activated carbon with oxidizing agents. These changes were more pronounced in case of oxidation with $HNO_3$. The surface pH of un-oxidized carbon was basic whereas those of the oxidized derivative were acidic. The removal of Cu(II) and Ni(II) was pH dependent and the maximum removal of the both ions was obtained at pH of 5-6. Cu(II) was more adsorbed, a phenomenon which was ascribed to its particular electronic configuration.

• 상하수도학회지
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• 제29권3호
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• pp.407-414
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• 2015

The effect of activated carbon particle diameter (i.e. US sieve No. $8{\times}10$ ($d_p{\approx}2.19mm$), $18{\times}20$ ($d_p{\approx}0.92mm$), $50{\times}60$ ($d_p{\approx}0.27mm$) and $170{\times}200$ ($d_p{\approx}0.081mm$) on caffeine adsorption is investigated. BET surface area was increased with decreasing particle diameter ($d_p$), and caffeine adsorption rates increased with decreasing $d_p$. Moreover, pseudo-second order model is predicted the experimental data more accurately than pseudo-first order model, and the fastest rate constant ($k_2$) was $1.7g\;mg^{-1}min^{-1}$ when $d_p$ was 0.081 mm. Surface diffusion coefficient (Ds) was decreased with decreasing $d_p$ based on the minimum sum of square error (SSE). Practically, certain ranges of Ds are acceptable with high reliability ($R^2$) and it is determined that the effect of $d_p$ on Ds is unclear. The effect of pH on caffeine adsorption indicated the dependency of m/L ratio (mass liquid ratio) and $pH_{pzc}$. The $pH_{pzc}$ (i.e. $7.9{\pm}0.2$) was not affected by $d_p$. The higher caffeine adsorption at pH 4 and pH 7 than at pH 10 is due to $pH_{pzc}$, not $pk_a$ of caffeine.

• 상하수도학회지
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• 제37권4호
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• pp.177-186
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• 2023

Perfluorooctanoic acid(PFOA) was one of widely used per- and poly substances(PFAS) in the industrial field and its concentration in the surface and groundwater was found with relatively high concentration compared to other PFAS. Since various processes have been introduced to remove the PFOA, adsorption using GAC is well known as a useful and effective process in water and wastewater treatment. Surface modification for GAC was carried out using Cu and Fe to enhance the adsorption capacity and four different adsorbents, such as GAC-Cu, GAC-Fe, GAC-Cu(OH)₂, GAC-Fe(OH)₃ were prepared and compared with GAC. According to SEM-EDS, the increase of Cu or Fe was confirmed after surface modification and higher weight was observed for Cu and Fe hydroxide(GAC-Cu(OH)₂ and GAC-Fe(OH)₃, respectively). BET analysis showed that the surface modification reduced specific surface area and total pore volumes. The highest removal efficiency(71.4%) was obtained in GAC-Cu which is improved by 17.9% whereas the use of Fe showed lower removal efficiency compared to GAC. PFOA removal was decreased with increase of solution pH indicating electrostatic interaction governs at low pH and its effect was decreased when the point of zero charges(pzc) was negatively increased with an increase of pH. The enhanced removal of PFOA was clearly observed in solution pH 7, confirming the Cu in the surface of GAC plays a role on the PFOA adsorption. The maximum uptake was calculated as 257 and 345 ㎍/g for GAC and GAC-Cu using Langmuir isotherm. 40% and 80% of removal were accomplished within 1 h and 48 h. According to R², only the linear pseudo-second-order(pso) kinetic model showed 0.98 whereas the others obtained less than 0.870.

• 한국산학기술학회논문지
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• 제18권4호
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• pp.584-591
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• 2017

수중에서 중금속은 흡착제에 의한 표면흡착과 금속수산화물로의 침전/제거반응이 동시에 일어나기 때문에 이들 각각에 의한 중금속 제거기작은 명확하게 구분되어 설명되지 못한다. 본 연구에서는 중금속 제거기작을 보다 명확하게 이해하기 위해 $850^{\circ}C$로 소성된 황토를 이용하여 다양한 pH 조건에서 Cu, Pb, Zn, Cd, 그리고 Cr 수용액 각각을 대상으로 회분식실험을 수행하였다. 실험결과 Cr을 제외한 중금속 농도는 반응초기에(<5분) 급격하게 감소되어 초기농도 대비 약 90%가 제거되었다. 한편, pH는 대상 금속 수용액에 따라 정도의 차이를 보이긴 하나 전체적으로 반응시간에 따라 지속적으로 증가되어 7.0-9.0까지 증가되었다. 반응시간에 따라 증가되는 pH 값과 높은 pH 조건에서 상대적으로 높은 중금속 제거율은 금속수산화물의 침전과 관련 있어 보인다. 흡착제(상용활성탄, 비소성황토, 소성황토)별 반응시간에 따른 pH 변화에 대한 비교실험결과, pH 증가현상은 소성황토에서만 두드러지게 나타나 소성과정에서 황토의 물성특성이 변화되었던 것으로 생각된다. 따라서 소성황토에 의한 중금속 제거는 흡착제에 의한 단순흡착뿐 아니라, 높은 pH 조건에서 금속수산화물을 형성함으로써 흡착질 표면에 침전 제어 될 수 있음을 보여준다.