• Transactions of the Korean hydrogen and new energy society
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• v.22 no.5
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• pp.714-720
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• 2011

Ethanol was used as reducing agent to remove $NO_x$ exhaust from the stationary source. Pre-treatment with sulfuric acid over $Ag/Al_2O_3$ catalyst was dedicated to overcome the $SO_2$ poisoning effect. The $NO_x$ reduction experiment was performed under the simulated condition of power plant The increased surface area with higher CPSI devoted to increase de-$NO_x$ yield. De-$NO_x$ yield of the $NO_x$ exhaust containing 20 ppm of $SO_2$ increased after acid treatment with 0.7% $H_2SO_4$ over 4.0% $Ag/Al_2O_3$, where the increased dispersion of Ag found from the results of XRD and XPS was the dominant factor for the increased de-$NO_x$ yield. However, the reason for the decreased de-$NO_x$ yield with the acid treatment of higher concentration (1.0% and 2.0%) of $H_2SO_4$ was found to be due to the formation of $Ag_2SO_4$ crystallites found from XRD result. Acid-treated $Ag/Al_2O_3$ catalyst showed maximum de-$NO_x$ yield at higher temperature than non-treated $Ag/Al_2O_3$ catalyst did.

• Journal of Power System Engineering
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• v.20 no.3
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• pp.17-21
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• 2016

The corrosion behavior of aluminum alloys in the $H_2SO_4$ solution was investigated based on potentiodynamic techniques. Electrochemical properties, such as corrosion potential($E_c$), passive potential($E_p$), corrosion current density($I_c$), corrosion rate(mpy), of Al-Mg-Si, Al-Cu-Si and Al-Si alloys were characterized at room temperature. Passive aluminum oxide film, which including $Al_2(SO_4)_3$ and $3Al_2O_34SO_38H_2O$, were uniformly formed on the surface via the reaction of Al with $SO{_3}^{2-}$ or $SO{_4}^{2-}$ ions in the $H_2SO_4$ solution and the dependence of the corrosion behavior on the alloying element was discussed. The selective leaching of alloy element increased with increasing Cu content in the aluminum alloys.

• Journal of the Korean Recycled Construction Resources Institute
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• v.12 no.2
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• pp.121-127
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• 2024

In this study, the applicability of replacing DG(Desulfurized Gypsum) from oil refinery with CCCMs(Carbon dioxide Conversion Capture Materials) as an ALC(Auto-claved LIghtweight Concrete) raw material was examined, and basic properties of ALC was measured. The main chemical components of DG and CCCMs were CaO and SO₃, and an increase in LOI(Loss of ignition) due to mineral carbonation reaction was verified. The crystalline phases of CCCMs were CaCO₃, CaSO₄, Ca(OH)₂, and CaSO₄·2H₂O. When DG, a raw material for ALC production, was replaced with CCCMs, foaming height, pore shape, absolute dry gravity, and compressive strength results measured similar for all binders. In addition, the formation of tobermorite which is main crystalline phase of ALC was shown for all specimens in microstructural analysis.

• Carbon letters
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• v.18
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• pp.43-48
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• 2016

Sulphonated polysulphone (SPS) has been synthesized and subsequently applied as binder for graphene oxide (GO)-based electrodes for development of electrochemical supercapacitors. Electrochemical performance of the electrode was investigated using cyclic voltammetry in 1M Na₂SO₄ and 1M KOH solution. The fabricated supercapacitors gave a specific capacitance of 161.6 and 216.8 F/g with 215.4 W/kg and 450 W/kg of power density, in 1M Na₂SO₄ and 1M KOH solutions, respectively. This suggests that KOH is a better electrolyte than Na₂SO₄ for studying the electrochemical behavior of electroactive material, and also suggests SPS is a good binder for fabrication of a GO based electrode.

• Kyungpook Mathematical Journal
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• v.63 no.2
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• pp.287-311
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• 2023

In this paper, we introduce the notion of cyclic structure Jacobi semi-symmetric real hypersurfaces in the complex hyperbolic quadric Q^m* = SO⁰_2,m/SO₂SO_m. We give a classifiction of when real hypersurfaces in the complex hyperbolic quadric Q^m* having 𝔄-principal or 𝔄-isotropic unit normal vector fields have cyclic structure Jacobi semi-symmetric tensor.

• Applied Chemistry for Engineering
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• v.16 no.6
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• pp.848-852
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• 2005

The two important problems to solve before the industrialization of the iodine-sulfur (IS) process are (i) methods to separate $H_2SO_4$ and HI and (ii) to maintain constant components. However undesired reaction was occurred and $H_2S$ and S were formed during the Bunsen reaction. It is necessary to forbid the undesired reaction between $H_2SO_4$ and HI by separating the two acids into two different layers. The experimental conditions for the present study was chosen in such a way that to achieve the separation between the two acids and minimize the side reaction. $H_2S$ formation was reduced and the separations of the two liquids were occurred at $H_2O$ molar fraction from 0.86 to 0.909. But the separations between the two liquids were not occurred at $H_2O$ molar fraction more than 0.92.

• Korean Journal of Remote Sensing
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• v.38 no.2
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• pp.189-198
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• 2022

In this present study, we investigated the effect of the offset correction factor calculation method on the sulfur dioxide (SO₂) column density in the SO₂ retrieval algorithm of the Geostationary Environment Monitoring Spectrometer (GEMS) launched in February 2020. The GEMS operational SO₂ retrieval algorithm is the Differential Optical Absorption Spectroscopy (DOAS) - Principal Component Analysis (PCA) Hybrid algorithm. In the GEMS Hybrid algorithm, the offset correction process is essential to correct the absorption effect of ozone appearing in the SO₂ slant column density (SCD) obtained after spectral fitting using DOAS. Since the SO₂ column density may depend on the conditions for calculating the offset correction factor, it is necessary to apply an appropriate offset correction value. In this present study, the offset correction values were calculated for days with many cloud pixels and few cloud pixels, respectively. And a comparison of the SO₂ column density retrieved by applying each offset correction factor to the GEMS operational SO₂ retrieval algorithm was performed. When the offset correction value was calculated using radiance data of GEMS on a day with many cloud pixels was used, the standard deviation of the SO₂ column density around India and the Korean Peninsula, which are the edges of the GEMS observation area, was 1.27 DU, and 0.58 DU, respectively. And around Hong Kong, where there were many cloud pixels, the SO₂ standard deviation was 0.77 DU. On the other hand, when the offset correction value calculated using the GEMS data on the day with few cloud pixels was used, the standard deviation of the SO₂ column density slightly decreased around India (0.72 DU), Korean Peninsula (0.38 DU), and Hong Kong (0.44 DU). We found that the SO₂ retrieval was relatively stable compared to the SO₂ retrieval case using the offset correction value on the day with many cloud pixels. Accordingly, to minimize the uncertainty of the GEMS SO₂ retrieval algorithm and to obtain a stable retrieval, it is necessary to calculate the offset correction factor under appropriate conditions.

• Corrosion Science and Technology
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• v.20 no.2
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• pp.77-84
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• 2021

This study aims to optimize the DL-EPR test solution for duplex stainless steel S31083 using the Taguchi design. The test solution parameters applied to the Taguchi design are H₂SO₄, NaCl, KSCN concentration, and temperature. In the experimental design, an orthogonal array of 4 levels 4 factor L₁₆(4⁴) was used. Output values for the orthogonal array were used for resolution (degree of sensitization) and selective etch (I_a) values. The optimal test solution conditions were selected by comparing the normalized S/N ratio for the two reaction properties. As a result, the H₂SO₄ and NaCl were identified as the main factors influencing the sensitivity measurement, but the delta statistics showed that the KSCN concentration and temperature had relatively low influence. The optimal condition was identified as 1.5 M H₂SO₄+0.03 M KSCN+1.5M NaCl at 30 ℃. The degree of sensitization presented a tendency to depend on the heat treatment temperature and time in the optimal test solution. This investigation confirmed the possibility of optimizing the experiment solution for the DL-EPR test of stainless steel using the Taguchi technique.

• Ocean and Polar Research
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• v.44 no.4
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• pp.297-310
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• 2022

To understand the chemical composition of aerosols in the Cheju-Korea Straits and their contribution to the ocean by deposition, aerosol samples were collected on board R/V Eardo from November 1997 to May 1999. The average concentrations of Al, NO₃^-, non-sea-salt (nss)-SO₄^2-, and NH₄⁺ in aerosols were 2.19, 5.59, 6.16 and 2.08 ㎍ m^-3, respectively. The Al concentration in the high yellow dust period was about 100 times higher than that in the non-yellow dust period. The concentration ratio of NO₃^-/nss-SO₄^2- ranged between 0.47 and 1.5, indicating that the aerosols in the Cheju-Korea Straits are under the effects of NO_x and SO_x emitted from China, Korea and Japan. The equivalent concentration ratio of [NH₄⁺]/[nss-SO₄^2-+ NO₃^-] with the average of 0.58±0.29 indicates that nss-SO₄^2- and NO₃^- are not neutralized by NH₄⁺. A high activity concentration of ²¹⁰Pb with 1.13-1.23 mBq m^-3 was observed during the high yellow dust period, indicating that ²¹⁰Pb is easily adsorbed in the yellow dust originating from the continent of Asia. The distribution of ⁷Be and NH₄⁺ concentrations showed a strong negative linear correlation during the low yellow dust period, April 1998. The total mineral dust flux in the Cheju-Korea Straits was estimated to be 1.21×10⁶ tons yr^-1, accounting for about 12% of the annual sediment discharge via the Nakdong River. The combined annual deposition of NH₄⁺ and NO₃^- was 0.103 mole N m^-2 yr^-1 was estimated to support 4% of the annual primary productivity in the East China Sea.

• Journal of Environmental Science International
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• v.29 no.10
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• pp.943-949
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• 2020

In this work, we prepared a heterojunction anode with a surface layer of SnO₂-Sb-Ni (SSN) on a Ti/IrO₂ electrode by thermal decomposition to improve the electrochemical activity of the Ti/IrO₂ electrode. The Ti/IrO₂-SSN electrode showed significantly improved electrochemical activity compared with Ti/IrO₂. For the 0.1 M NaCl and 0.1 M Na₂SO₄ electrolytes, the onset potential of the Ti/IrO₂-SSN electrode shifted in the positive direction by 0.1 V_SCE and 0.4 V_SCE, respectively. In 2.0-2.5 V voltages, the concentration in Ti/IrO₂-SSN was 2.59-214.6 mg/L Cl₂, and Ti/IrO₂ was 0.55-49.21 mg/L Cl₂. Moreover, the generation of the reactive chlorine species and degradation of Eosin-Y increased by 3.79-7.60 times and 1.06-2.15 times compared with that of Ti/IrO₂. Among these voltages, the generation of the reactive chlorine species and degradation of Eosin-Y were the most improved at 2.25 V. Accordingly, in the Ti/IrO₂-SSN electrode, it can be assumed that the competitive reaction between chlorine ion oxidation and water oxidation is minimized at an applied voltage of 2.25V.