• Journal of the Korea Academia-Industrial cooperation Society
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• v.15 no.11
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• pp.6952-6957
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• 2014

In photocatalysis, the addition of metal matter to $TiO_2$ can alter the surface properties. As such, the metal can increase the rate of the photodegradation reaction. In this study, a range of modified $TiO_2$ photocatalysts were prepared and tested to improve the activity of photodegradation at a batch-typed photoreactor. To obtain a good sol solution of the $TiO_2$ photocatalyst, several types of dispersion agents and stabilizers were investigated. The photocatalyst solutions were modified with isoproply alcohol as the dispersion agent and sodium silicate as the stabilizer. The effects of various metallic elements on enhancing the photocatalytic activity of $TiO_2$ on the degradation of toluene were examined. Palladium-added $TiO_2$ was found to be the best, whereas copper or tungsten-added also showed good results. In the case of palladium addition, the increase in removal efficiency was 25%. On the other hand, Fe-added $TiO_2$ showed a notable decrease in photocatalytic degradation. Additional doping of copper or tungsten on the $Pd/TiO_2$ had no positive effect on the photodegradation activity.

• Journal of Electrochemical Science and Technology
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• v.11 no.3
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• pp.273-281
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• 2020

Constructing and making highly active and stable nanostructured Pt-based catalysts with ultralow Pt loading are still electrifying for electrochemical applications such as water electrolysis and fuel cells. In this study, MoO₃ ribbons (RBs) of few micrometer in length is successfully synthesized via hydrothermal synthesis. Subsequently, 3-dimentional (3D)-silicate layer for about 10 to 15 nm is introduced via chemical deposition onto the pre-formed MoO₃ RBs; to setup the platform for Pt metaldots (MDs) deposition. In comparison with the bare MoO₃ RBs, the MoO₃-Si has served as a efficient solid-support for stabilizing and accommodating the uniform deposition of sub-2 nm Pt MDs. Such a structural design would effectively assist in improving the electronic conductivity of a fabricated MoO₃-Si-Pt catalyst towards MOR; the interfaced, porous and 3D silicate layer has assisted in an efficient mass transport and quenching the poisonous CO_ads species leading to a significant electrocatalytic performance for MOR in alkaline medium. Uniformly decorated, sub-2 nm sized Pt MDs has synergistically oxidized the MeOH in association with the MoO₃-Si solid-support hence, synergistic catalytic activity has been achieved. Present facile approach can be extended for fabricating variety of highly efficient Metal Oxide-Metal Nanocomposite for energy harvesting applications.

• Clean Technology
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• v.12 no.3
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• pp.171-174
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• 2006

The adsorbent for removal of heavy metal ions is prepared reutilizing the leached sludge generated in process of making the red mud coagulant we have develope. The pellet-type adsorbent is made by heat-treating a mixture of 10g of the leached sludge, 1g of kaolin, and 2 g of sodium silicate solution at $600^{\circ}C$ for 2 hours. In experiments of batch adsorption, the adsorbent shows good performance in adsorption of $Pb^{2+}$ ion.

• Transactions on Electrical and Electronic Materials
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• v.12 no.3
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• pp.127-130
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• 2011

We investigated the effects of $O_2$ annealing (i.e., temperature and time) on the characteristics of hafnium silicate ($HfSi_xO_y$) films deposited on a Si substrate by atomic layer deposition process (ALD). We found that the post deposition annealing under oxidizing ambient causes the oxidation of residual Hf metal components, resulting in the improvement of electrical characteristics (e.g., hysteresis window and leakage current are decreased). In addition, we observed the annealing temperature is more important than the annealing time for post deposition annealing. Based on these observations, we suggest that post deposition annealing under oxidizing ambient is necessary to improve the electrical characteristics of $HfSi_xO_y$ films deposited by ALD. However, the annealing temperature has to be carefully controlled to minimize the regrowth of interfacial oxide, which degrades the value of equivalent oxide thickness.

• Journal of the Korean Institute of Electrical and Electronic Material Engineers
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• v.14 no.10
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• pp.779-784
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• 2001

In this work, we studied the characteristics of nitride films for the optimization of PMD(pro-metal dielectric) linear process, which can be applied to the recent semiconductor manufacturing process. We split the deposit condition of nitride films into four parts such as PO(protect overcoat) nitride, baseline, low hydrogen and high stress and low hydrogen, respectively. We tried to find out correlation between BPSG deposition and densification. In order to analyze the changes of Si-H and Si-NH-Si bonding density, we used FTIR area method. We also investigated the crack generation on wafer edge after BPSG densification, and the changes of nitride film stress as a function of RF power variation to judge whether the deposited films.

• Journal of the Korean institute of surface engineering
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• v.47 no.4
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• pp.147-154
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• 2014

Formation behavior of PEO (Plasma Electrolytic Oxidation) films on AZ31 Mg alloy was studied in aqueous solutions containing various concentrations of hydroxide ion ($OH^-$) and silicate ion ($SiO_3{^{2-}}$) by voltage-time curves, and corrosion resistance of the PEO film-covered specimen was investigated by immersion test in 0.5 M NaCl solution. From the analyses of the voltage-time curves, it is suggested that two different types of anions are essentially needed for the formation of PEO films on AZ31 Mg alloy: film formation agent and local film breakdown agent. $SiO_3{^{2-}}$ ion acts only as a film formation agent but $OH^-$ ion acts not only as a film formation agent but also film breakdown agent. The PEO films prepared on AZ31 Mg alloy in alkaline silicate solution showed very good corrosion resistance without any pitting or filiform corrosions up to 480 h of immersion in 0.5 M NaCl.

• Proceedings of the Korean Vacuum Society Conference
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• 2013.02a
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• pp.546-546
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• 2013

Zinc silicate ($Zn_2SiO_4$) has been identified as a suitable host material for a wide variety of luminescent activators, such as transition metal and rare earth elements. In particular, manganese-activated $Zn_2SiO_4$ exhibits highly efficient photoluminescenceand cathodoluminescence, which allows this material to be used in fluorescent lamps and display applications. In this study, we investigated the green and yellow luminescence from Mn-doped $Zn_2SiO_4$ thin films that were synthesized using radio frequency magnetron sputtering followed by annealing at $600{\sim}1,200^{\circ}C$ The refractive index of the $Zn_2SiO_4$: Mn films showed normal dispersion behavior. It was found that the $Zn_2SiO_4$: Mn films annealed at $800^{\circ}C$ ossessed a mixture of alpha and beta phases. The obtained photoluminescence spectrum consisted of two emission bands centered at 525 nm in the green range and 574 nm in the yellow range. The green luminescence originates from the divalent Mn ions in alpha phase of $Zn_2SiO_4$, while the yellow luminescence comes from the divalent Mn ions in beta phase. The films annealed at and above $900^{\circ}C$ xhibited only the alpha phase. The broad PL excitation band was observed ranging from 220 to 300 nm with a maximum at around 243 nm.

• Journal of the Korean Chemical Society
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• v.46 no.6
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• pp.515-522
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• 2002

Solid beta-dicalcium silicate hydrate $(\beta-C_2SH)$ synthesized under hydrothermal conditions at $240^{\circ}C$ and Ca/Si=2 molar ratio shows cation exchange properties towards divalent metal cations such as Fe, Cu, Zn, Cd, or Pb. The ability of metal cation uptake by the solid was found to be in the order: $Fe^{2+}$〉$Cu^{2+}$〉$Zn^{2+}$〉$Cd^{2+}$ = $Pb^{2+}$. Cesium selectivity of the solid was demonstrated in the presence of univalent cation such as $Li^+$, $Na^+$ and $K^+$ and divalent cations such as $Ca^{2+}$, $Mg^{2+}$ and $Ba^{2+}$, which are one hundred times more concentrated than the $Cs^+$. The uptake of $Cs^+$ is maximum in the presence of $Mg^{2+}$ whereas it is minimum in the presence of $K^+$. The different affinities of ${\beta}-C_2SH$ towards divalent metal cations can be used for the separation of those ions. Due to its selectivity for cesium it can be used in partitioning of radioactive Cs+ from nuclear wastes containing numerous cations. The mechanism of the metal cation exchange and cesium selectivity reactions by the solid is studied.

• Economic and Environmental Geology
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• v.31 no.5
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• pp.365-374
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• 1998

Economic U- and Th-bearing pegmatite deposits occur in the Kyemyeongsan Formation, and are spatially closely associated with the Carboniferous alkali granite. The pegmatite is lithochemically alkaline and peralumious, and consists mainly of potassic feldspar and quartz with allanite and U- and Th-bearing minerals. Paragenetic stages of mineralization in the pegmatite are divided as follows: early silicate mineralization, main rare metal mineralization, and late silicate mineralization. Thorite, euxenite, fergusonite and uranpyrochlore are the predominant U- and Th-bearing minerals. Both the enrichments of Nb, Y, Th, U, and Ta and the depletions of Hf, Ba, and Rb in the pegmatite were resulted from magmatic differentiation. The increases of Na and Ca in uranpyrochlore, of Th and U in fergusonite, of Si, Th, U and Pb in thorite, and of Nb and Y in euxenite were possibly resulted from both later internal fractionation and hydrothermal alteration. The variation of chemical composition in a mineral species reflects the different pysico-chemical conditions during the crystallization.

• Journal of Korean Society for Atmospheric Environment
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• v.15 no.E
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• pp.9-16
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• 1999

This study has been focused on NO conversion for metal-incorporated silicates(Fe-silicate, Mn-silicate, and Fe-Mn-bimetallosilicate) with a similar MFI type. Used metallosilicates were prepared by the rapid crystallization method. Their catalytic performance for the conversion of NO under excess O2(10%) condition with the addition of hydrocarbon of low concentration(1,100ppm n-C8H18) were investigated. As a result, the NO conversion on the Fe-Mn-bimetallosilicate was enhanced compared with on the Fe- or Mn-silicates. Furthermore, the performances for NO concentration on Fe-Mn-bimetallosilicate more increased with an increased in n-C8H18 concentration, a decrease in NO concentration, and an increase in O2 concentration.