• Korean Chemical Engineering Research
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• v.59 no.2
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• pp.260-268
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• 2021

Adsorption is the most promising technology used to adsorb CO2 to reduce its concentration in the atmosphere due to its functional effectiveness. Various porous materials have been extensively synthesized to boost CO2 adsorption efficiency, for example, zeolite. Here, we report the synthesis process of zeolite adsorbent impregnated with amine, combining the benefit of these two substances. We compared conventional heating with microwave-assisted heating by varying concentrations of monoethanolamine in methanol (10% v/v and 40% v/v) as a liquid solution. The results showed that monoethanolamine impregnation helps significantly increase adsorption capacity, where adsorption occurs as a physisorption and not as chemisorption due to the adsorbent's steric hindrance effect. The highest adsorption capacity of 0.3649 mmol CO2 / gram adsorbent was reached by microwave exposure for 10 minutes. This work also reveals that a decrease in CO2 adsorption capacity was observed at a longer exposure period, and it reached a constant 40-minute adsorption rate. Impregnating activated zeolite with 40% monoethanolamine for 10 minutes in addition to microwave exposure (0.8973 mmol CO2 / gram adsorbent) is the maximum adsorption ability achieved.

• Proceedings of the Korean Vacuum Society Conference
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• 2012.02a
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• pp.246-246
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• 2012

Smart catalyst design though novel catalyst preparation methods can improve catalytic activity of transition metals on reducible oxide supports such as titania by enhancement of metal oxide interface effects. In this work, we investigated Pt nanoparticles/titania catalysts under CO oxidation reaction by using novel preparation methods in order to enhance its catalytic activity by optimizing metal oxide interface. Arc plasma deposition (APD) and metal impregnation techniques are employed to achieve Pt metal deposition on titania supports which are prepared by multi-target sputtering and Sol-gel techniques. In order to tailor metal-support interface for catalytic CO oxidation reaction, Pt nanoparticles and thin films are deposited in varying surface coverages on sputtered titania films using APD. To assess the role of oxide support at the interface, APD-Pt is deposited on sputtered and Sol-gel prepared titania films. Lastly, characteristics of APD-Pt process are compared with Pt impregnation technique. Our results show that activity of Pt nanoparticles is improved when supported over Sol-Gel prepared titania than sputtered titania film. It is suggested that this enhanced activity can be partly ascribed to a very rough titania surface with the higher free metal surface area and higher number of sites at the interface between the metal and the support. Also, APD-Pt shows superior catalytic activity under CO oxidation as compared to Pt impregnation on sputtered titania support. XPS results show that bulk oxide is formed on Pt when deposited through impregnation and has higher proportion of oxidized Pt in the form of $Pt^{2+/4+}$ oxidation states than Pt metal. APD-Pt shows, however, mild oxidation with large proportion of active Pt metal. APD-Pt also shows trend of increasing CO oxidation activity with number of shots. The activity continues to increase with surface coverage beyond 100%, thus suggesting a very rough and porous Pt films with higher active surface metal sites due to an increased surface area available for the reactant CO and $O_2$ molecules. The results suggest a novel approach for systematic investigation into metal oxide interface by rational catalysts design which can be extended to other metal-support systems in the future.

• Proceedings of the Korean Powder Metallurgy Institute Conference
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• 2006.09a
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• pp.301-302
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• 2006

Machinability and machining mechanism were examined in the case where resin impregnation treatment was conducted to the Mo-Co hardening particle dispersed iron-based sintered alloy. As a result, the force required for machining decreased significantly compared with the case where resin impregnation treatment was not conducted. This effect is considered to be attributable to the embrittlement of cutting chips produced by the minimization of the cut material deformation.

• Proceedings of the KAIS Fall Conference
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• 2006.05a
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• pp.565-568
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• 2006

Fe, Co, Zn, Cu, Pt 등의 전이금속과 ZSM-5 2종($SiO_2/Al_2O_3$ 몰비: 23, 50)과 ${\gamma}-alumina$를 담체로 사용하여 촉매를 합성하였다. 합성방법은 CVD(화학기상증착법) 과 Dry Impregnation (건식함침법), Incipient Wetness Impregnation방법이 있다. CVD 방법으로 얻은 Fe/ZSM-5과 Dry Impregnation방법으로 얻은 Cu/ZSM-5은 NO저감효율에 있어 거의 비슷하였다. 지지체로 사용된 ZSM-5의 $SiO_2/Al_2O_3$의 몰 비가 작을수록, 즉 산점의 수가 많을수록 우수한 것으로 보인다.

• Bulletin of the Korean Chemical Society
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• v.29 no.12
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• pp.2434-2440
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• 2008

The effect of sodium (Na) promotion was studied in the biphenol (BP) hydrogenation using various Pd/C catalysts. Different amounts of sodium metal were used for promotion with Pd/C and their effects on BP hydrogenation were observed. The promotion order was changed to compare the effect of the position of the promoter in relation to the palladium (Pd) metal on the catalytic activity and yield of the final product, bicyclohexyl-4,4'-diol (BHD). Pd/C catalysts prepared from different methods were also sodium-promoted and the changes of the reaction pathway according to the type of promoted Pd/C catalyst were compared.

• Applied Chemistry for Engineering
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• v.16 no.3
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• pp.312-316
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• 2005

Adsorption characteristics of $CO_2$ on activated carbons were evaluated using dynamic adsorption method in a fixed bed with acid treatment, LiOH impregnation and water vapor supply. Physical and chemical properties of the activated carbons were measured using SEM, EDS, nitrogen adsorption, FTIR and XRD. Nitric acid treatment led to the decrease in BET surface area and the increase in oxygen content of virgin activated carbon, and it produced a new functional group that included nitrogen. For the reduction of BET surface area by LiOH impregnation, the nitric acid treated activated carbon (NAC) was less than the virgin activated carbon (AC). Large particles of LiOH were present on the carbon surface when the content of LiOH was over 2 wt%. The adsorbed amount of $CO_2$ on activated carbon in a fixed bed increased with the acid treatment, LiOH impregnation and water vapor supply. The XRD results indicated that LiOH was converted to $Li_2CO_3$ after the adsorption of $CO_2$ on LiOH precursor.

• Journal of the Korean Wood Science and Technology
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• v.38 no.3
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• pp.178-184
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• 2010

This study was carried out to investigate the properties of woodceramics made from woody part of Broussonetia Kazinoki at different impregnation ratios of phenolic resin of 40, 50, 60, 70%. The physical and mechanical properties increased with increasing impregnation ratio. The highest mean values of density, bending strength, Brinell hardness and compressive strength were 0.66 g/$cm^3$, 53 kgf/$cm^2$, 187 kgf/$cm^2$, 126 kgf/$cm^2$, respectively. There were close correlations between density and bending strength, Brinell hardness and compressive strength, and between MOE and MOR.

• Journal of Korean Society for Atmospheric Environment
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• v.25 no.4
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• pp.316-324
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• 2009

Carbon based sorbents for $CO_2$ adsorption were prepared by impregnation with alkali metals ($Li^+$, $K^+$) and alkaline earth metals ($Ca^{2+}$, $Mg^{2+}$). BET surface area of test sorbents was lower than the intrinsic activated carbon. In particular, impregnation of $Ca^{2+}$ or $Mg^{2+}$ resulted in lower surface area of specific adsorption sites than that of $Li^+$ or $K^+$. While the adsorption capacity for $CO_2$ was high in the sorbents containing $Ca^{2+}$ and $Mg^{2+}$, strong interaction with $CO_2$ would cause to drop the capacity after regeneration. The adsorption was found high relatively in the flow with a high concentration of $CO_2$ and in a low flow rate. The adsorption isotherm for the present modified AC sorbents fits well with the Freundlich model.

• Journal of Environmental Science International
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• v.22 no.7
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• pp.847-853
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• 2013

Functionalized adsorbent has been synthesized by piperazine(Pz) on activated carbon. Quantitative estimations of $CO_2$ were undertaken using gas chromatography with GC/TCD and the prepared adsorbents were characterized by BET surface area and FT-IR. It was also studied effect of various parameters such as piperazine loadings and adsorption temperature. The specific surface area decreased from $1212.0m^2/g$ to $969.8m^2/g$ by impregnation and FT-IR revealed a N-H functional group at about $1400cm^{-1}$ to $1700cm^{-1}$. The $CO_2$ adsorption capacity at $20^{\circ}C$ and $50{\sim}100^{\circ}C$ was as follow: AC > Pz(10)-AC> Pz(30)-AC> Pz(50)-AC at $20^{\circ}C$ and Pz(10)-AC > AC > Pz(30)-AC> Pz(50)-AC at $50{\sim}100^{\circ}C$. Therefore, for high temperature flue gas condition, the Pz(10)-AC showed the highest adsorption capacity due to physical adsorption and chemical adsorption by amino-group content. The results suggest that activated carbon impregnated with Pz is an effective adsorbent for $CO_2$ capture from real flue gases above $50^{\circ}C$.

• Korean Chemical Engineering Research
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• v.53 no.3
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• pp.382-390
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• 2015

Poly(methyl methacrylate) (PMMA) supports and amine additives were investigated to adsorb $CO_2$. PMMA supports were fabricated by using different ratio of pore forming agents (porogen) to control the BET specific surface area, pore volume and distribution. Toluene and xylene are used for porogens. Supported amine sorbents were prepared by wet impregnation of tetraethylenepentamine (TEPA) on PMMA supports. So we could identify the effect of the pore structure of supports and the quantity of impregnated TEPA on the adsorption capacity. The increased amount of toluene as pore foaming agent resulted in the decreased average pore diameter and the increased BET surface area. Polymer supports with huge different pore distribution could be fabricated by controlling the ratio of porogen. After impregnation, the support with micropore structure is supposed the pore blocking and filling effect so that it has low $CO_2$ capacity and kinetics due to the difficulty of diffusing. Macropore structure indicates fast adsorption capacity and low influence of amine loading. In case of support with mesopore, it has high performance of adsorption capacity and kinetics. So high surface area and meso-/macro- pore structure is suitable for $CO_2$ capture.