• Journal of the Korean Chemical Society
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• v.36 no.3
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• pp.351-359
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• 1992

Interaction of xenon with alkaline-earth cations in Y zeolite supercage was studied by xenon adsorption and $^{129}Xe$ NMR experiments. The CaY and the BaY samples were prepared by exchanging $Ca^{2+}$ and $Ba^{2+}$ into a high-purity NaY zeolite. Xenon adsorption isotherms of these samples were obtained by using a conventional volummetric gas adsorption apparatus in the range of 260 to 320 K and the chemical shift in the $^{129}Xe$ NMR spectrum of the adsorbed xenon was measured at 296 K. The chemical shift against pressure was quantitatively explained assuming that the xenon gas exchanged very rapidly between various adsorption sites consisting of zeolite-framework surface and alkaline-earth ion. From this analysis, it was found that the alkaline-earth ion adsorbed xenon more strongly than $Na^+$ ion and zeolite-framework surface. Baring on the difference of the adsorption strength, the number of the alkaline-earth cations present in the zeolite supercage could be estimated by analyzing the adsorption isotherm.

• Proceeding of EDISON Challenge
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• 2017.03a
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• pp.484-486
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• 2017

포스포린에 대한 관심이 높아지면서 그 기계적 성질을 아는 것이 중요해졌다. 포스포린의 표면에 알칼리 금속 원자를 흡착시켰을 때, 그렇지 않았을 때보다 강성이 감소하는 것이 계산되었다. 또한 흡착된 원자의 절대적인 크기가 클수록 강성을 더욱 감소시킬 수 있음을 암시하는 결과가 발견되었다.

• Analytical Science and Technology
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• v.11 no.4
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• pp.248-253
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• 1998

The adsorption and separation behaviors of alkali, alkaline earth and transition metal ions using a poly-dibenzo-18-crown-6 were investigated in aqueous solution. The adsorption degree(E) and distribution ratio(D) of alkali, alkaline earth metal ions were Li(I)$t_R$) of metal ions were affected by the adsorption degree(E) and distribution ratio(D). This results showed good separation efficiency of K(I), Sr(II), Ag(I) and Pb(II) from the mixed metal solution.

• Applied Chemistry for Engineering
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• v.9 no.2
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• pp.286-293
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• 1998

Two methods were used to enhance the adsorption capacity of activated carbons. One is to impregnate activated carbons with chemical compounds which have a good affinity for $CO_2$. The other is to activate by heat-treating after impregnation with KOH on activated carbons(AC). The chemical compounds impregnated on AC were alkali metal, alkaline earth metal, and transition metal chlorides. The adsorption capacity of $CO_2$ on AC impregnated with these metals was less than that of pure AC. These compounds have not the chemical affinity for $CO_2$ and obstruct the micropore of AC. The experiment of breakthrough for $CO_2$ on AC impregnated with KOH showed the increase of the adsorbed amount of $CO_2$ in influent gases containing water vapor. This means that KOH adsorbes $CO_2$ gas. However, the adsorbents impregnated with KOH had not the reproducibility because of the production of $K_2CO_3$ by the reaction of KOH with $CO_2$. The amount of $CO_2$ adsorbed on the heat-treated AC at $800^{\circ}C$ increased with the amount of impregnation. The adsorption capacity of $CO_2$ was the largest when the ratio of weight of KOH to AC equal to 4. The isosteric heat of adsorption was calculated by the equation of Clausius-Clapeyron form adsorption capacity data of $CO_2$ for the temperature change. In addition, the characteristics of $CO_2$ breakthrough curve were surveyed for the change of flow rate and concentration.

• Journal of Energy Engineering
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• v.11 no.2
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• pp.114-121
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• 2002

Alkali metal compounds existed in original coal or sorbents are exhausted as vapor or small particle at the outlet of combustor when operating PFBC power plant. These compounds can be removed with dust removal equipment, but total generation efficiency will be decreased because of lower operating temperature of dust removal equipment. Alkali metal contained in vapor phase is initially deposited onto turbine blade results in serious corrosion. The concentration of alkali vapor in the PFBC flue gas is 20∼40 ppm which is dependent on mineral characteristics and composition as well as operating condition of PFBC. However, the allowance limit of alkali metal vapor is assigned as less than 50 ppb for gas turbine when coal or oil is used as fuel. Therefore, alkali metal vapor in PFBC or IGCC process should be removed by solid sorbents to prevent corrosion of turbine blade and improve plant efficiency. In the present investigation, powder of Bauxite, Kaolinite and Limestone is used in the preparation of cylinder-type pellet which is inserted into the pressurized alkali removal reactor for the alkali absorption experiment. Experimental results showed that the alkali removal efficiency in the order of Bauxite, Kaolinite and Limestone. Alkali vapor removal efficiency is related with reaction temperature, porosity of pellet and alkali vapor concentration of flue gas.

• Proceedings of the Mineralogical Society of Korea Conference
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• 2005.05a
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• pp.7-10
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• 2005

• Proceedings of the Korean Institute of Surface Engineering Conference
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• 2017.05a
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• pp.121-121
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• 2017

본 연구는 비전도성 폴리머 표면을 개질하여 감광성 금속을 유전체 표면에 흡착시키고, 감광성 금속의 광화학 반응을 이용하여 귀금속 촉매를 비전도성 폴리머 표면에 선택적으로 흡착시켜 무전해 Cu 도금을 수행하여 금속패턴을 형성하였다. 기능성 유연 필름은 일반적으로 투명한 플라스틱 고분자 기판을 기반으로 전기 전자, 에너지, 자동차, 포장, 의료 등 다양한 분야에서 폭넓게 활용 되고 있으며, 본 연구에서는 습식 도금 공정을 이용하여 폴리이미드 필름상에 $10{\mu}m$ 이하의 미세패턴을 형성하기 위한 공정을 개발하고자 하였다. 비전도성 폴리머 표면에 무전해 도금을 위해서 우선 폴리머 필름의 표면을 개질하는 공정이 필요하다. 이에 KOH 또는 NaOH 알카리 용액을 이용하여 표면을 개질하였으며 개질된 표면에 감광성 금속이온의 흡착시키기 위한 감광성 금속이온은 주석을 사용하였으며, 주석 용액의 안정성 및 퍼짐성 향상을 위해 감광성 금속 용액의 제조 및 특성을 관찰하였으며, 감광성 금속화합물이 흡착된 비전도성 유전체 표면을 포토마스크를 이용하여 특정 부위, 즉 표면에 금속패턴 층을 형성하고자 하는 곳은 포토마스크를 이용하여 광원을 차단하고 그 외 부분은 주 파장이 365nm와 405nm 광원을 조사하여 선택적으로 감광성 금속화합물의 산화반응을 유도하는 광조사 공정을 수행하였다. 광원이 조사되지 않은 부분에 귀금속 등의 촉매 입자를 치환 흡착시켜 금속 패턴이 형성될 수 있는 표면을 형성하였다. 위의 활성화 공정이후에 활성화 처리된 표면을 세척하는 수세 공정을 거친 후 무전해 도금공정에 바로 적용할 경우 미세한 귀금속 입자가 패턴이 아닌 부분 즉 자외선(UV) 조사된 부분에도 남아있어 도금시 번짐 현상이 발생한다. 이에 본 연구에서는 활성화 처리 후 약 알칼리 용액에 카르복실산을 혼합하여 잔존하는 귀금속 입자를 제거한 후 무전해 Cu 도금액을 이용하여 $10{\mu}m$ 이하의 Cu 금속 패턴을 형성하였다.

• Journal of the Korea Organic Resources Recycling Association
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• v.15 no.4
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• pp.107-114
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• 2007

A study on the removal of heavy metals using alginic acid, a kind of polysaccharides, was performed. Alginic acid adsorbed 480 mg Pb/g dry mass at pH 4, which was about twice as high as uptake capacity of other biosorbents. Isothermal adsorption curve for lead ions was described by the Langmuir model equation and the experimental data well fitted to model equation. The adsorption of lead ions was an endothermic process since binding strength increased with temperature. The effect of alkali metal ions ($Ca^{2+}$ and $Mg^{2+}$) on lead sorption capacity was negligible and most adsorption process was completed in 30min. The uptake capacity of other metals such as, copper, mercury, strontium, and cesium ions using alginic acid was also investigated.

• Applied Chemistry for Engineering
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• v.5 no.6
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• pp.1024-1029
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• 1994

The characteristics of the nitrogen adsorption with natural zeolite produced in Kampo area according to the chemical treatment by HCl and/or NaOH or the exchanging metal ion were investigated in the pressure range of 100~760torr at $25^{\circ}C$. The amount of nitrogen adsorption was followed at increment in the order of NaOH treatment>nontreatment>HCl treatment. Adsorption amount on natural zeolite treated with 0.5N-HCl/NaOH was improved about 200%, whereas that on natural zeolite treated with 0.5N-NaOH/HCl was decreased. When metal ion of natural zeolite was exchanged with $Na^+$, $K^+$ and $Cs^+$, adsorption amount of nitrogen was decreased as the size of cation was increased. But metal ion of natural zeolite was exchanged with $Mg^{2+}$, $Ca^{2+}$ and $Ba^{2+}$, the amount of nitrogen adsorption was increased.

• Journal of the Korean Vacuum Society
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• v.6 no.2
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• pp.159-164
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• 1997

We have studied initial oxidation of the alkali metal(AM)/Si(111) surface using X-ray photoelectron spectroscopy(XPS) and reflection high energy electron diffraction(RHEED) at room temperature(RT) and high temperature(HT)(300~50$0^{\circ}C$). The oxidation of the Si(111)7$\times$7 surface was promoted by the adsorption of 1 momolayer(ML) AM, whereas no promotion occurred for submonolayer(<0.5 ML) adsorbed Si(111)7$\times$7 surface at RT. O Is core level spectra were measured with increasing oxygen exposure. It was found that the oxygen adsorbed on the Si(111)7$\times$7-AM surface have two different bond configuration, Si-O and Am-O, respectively. From these results, we discussed the role of AM-O bonding in the promoted oxidation. At HT(300~50$0^{\circ}C$), the AM-adsorbed surface became very inactive with the structural transformation to the 3$\times$1-AM. We present the results of the oxidation of the Si(111)3$\times$1-AM(Na, K, Cs) surface.