• 한국재료학회:학술대회논문집
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• 한국재료학회 2010년도 춘계학술발표대회
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• pp.43.2-43.2
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• 2010

Most of previous methods for the dispersions of carbon nanotube were achieved by various chemical functionalizations. In this study, however, we generated highly water dispersed carbon nanofibers by altering intrinsic materials property only, such as crystallinity of outer layers of carbons, without chemical treatment. Although most of chemical functionalization requires acidic treatment and may degrade their chemical functions by interacting with other molecules, suggested strategy demonstrated a simple but chemically non-degradable carbon nanotube for the application of various medical applications, such as drug delivery system and implant coatings.Furthermore, protein adsorption was increased by the reducing surface crystalinity since outer activated surface induced more adsorption of oxygen and eventually greater protein adsorption than pristine carbon nanofibers.

• 분석과학
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• 제17권1호
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• pp.82-84
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• 2004

The quantitative trace analysis of ions could be deteriorated by filter papers because of the effect of adsorption. Generally the adsorption of anions on filter paper did not occurred. Instead, $Cl^-$ and $NO{_3}^-$ ions were extracted from the filter papers. However, most metal ions were adsorbed on the filter papers by the formation of hydroxide in neutral solution. The adsorption of metal ions except $Ag^+$ ion could be avoided depend on the acid concentrations.

• Carbon letters
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• 제7권2호
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• pp.97-104
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• 2006

The influence of carbon surface area, carbon-oxygen groups associated with the carbon surface and the solution pH on the adsorption of Pb(II) ions from aqueous solutions has been studied using three activated carbons. The adsorption isotherms are Type I of BET classification and the data obeys Langmuir adsorption equation. The BET surface area has little effect on the adsorption while it is strongly influenced by the presence of acidic carbon oxygen surface groups. The amount of these surface groups was enhanced by oxidation of the carbons with different oxidizing agents and reduced by eliminating these groups on degassing at different temperatures. The adsorption of Pb(II) ions increases on each oxidation and decreases on degassing the oxidized carbons. The increase in adsorption on oxidation has been attributed to the formation of acidic carbon-oxygen surface groups and the decrease to the elimination of these acidic surface groups on degassing. The adsorption is also influenced by the pH of the aqueous solution. The adsorption is only small at pH values lower than 3 but is considerably larger at higher pH values. Suitable mechanisms consistent with the adsorption data have been suggested.

• 한국환경과학회지
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• 제22권12호
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• pp.1651-1660
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• 2013

The adsorption of lithium ion onto zeolite was investigated depending on contact time, initial concentration, cation forms, pH, and adsorption isotherms by employing batch adsorption experiment. The zeolite was converted into different forms such $K^+$, $Na^+$, $Mg^{2+}$, $Ca^{2+}$, and $Al^{3+}$. The zeolite had the higher adsorption capacity of lithium ion in $K^+$ form followed by $Na^+$, $Ca^{2+}$, $Mg^{2+}$, and $Al^{3+}$ forms, which was in accordance with their elctronegativities. The lithium ion adsorption was explained using the Langmuir, Freundlich, and Dubinin-Radushkevich adsorption isotherms and kinetic models. Adsorption rate of lithium ion by zeolite modified in $K^+$ form was controlled by pseudo-second-order and particle diffusion kinetic models. The maximum adsorption capacity obtained from Langmuir isotherm was 17.0 mg/g for zeolite modified in $K^+$ form. The solution pH influenced significantly the lithium ions adsorption capacity and best results were obtained at pH 5-10.

• Bulletin of the Korean Chemical Society
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• 제35권8호
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• pp.2471-2476
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• 2014

The aim of the present study is to explore the possibility of utilizing loess for the adsorption of total phosphorous (T-P) and total nitrogen (T-N) in water. Batch adsorption studies were performed to evaluate the influences of various factors like initial concentration, contact time and temperature on the adsorption of T-P and T-N. The adsorption data showed that loess is not effective for the adsorption of T-N. However, loess exhibited much higher adsorption capacity for T-P. At concentration of $1.0mgL^{-1}$, approximately 97% of T-P adsorption was achieved by loess. The equilibrium data were fitted well to the Langmuir isotherm model. The pseudo-second-order kinetic model appeared to be the better-fitting model because it has higher $R^2$ compared with the pseudo-first-order and intra-particle kinetic model. The theoretical adsorption equilibrium $q_{e,cal}$ from pseudo-second-order kinetic model was relatively similar to the experimental adsorption equilibrium $q_{e,exp}$. The thermodynamic parameters such as free energy ${\Delta}G$, the enthalpy ${\Delta}H$ and the entropy ${\Delta}S$ were also calculated.

• 공업화학
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• 제28권5호
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• pp.539-546
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• 2017

본 연구는 산성유해가스 제거를 위한 고효율 음이온교환 복합 폼 화학필터를 제조하기 위하여 폴리우레탄(PU) foam에 다른 종류의 PSA를 사용하여 상용이온교환수지를 부착하여 제조, 이의 내수성, 내화학성, 접착신율, 농도와 유속에 따른 HCl과 HF의 흡착특성에 관하여 연구하였다. 그 결과 접착신율은 ATE-701은 900%, AT-4000C는 1,500%, HCA-1000는 2,400%이며, 내수성 및 내화학성평가에서 HCA-1000의 탈리율이 6% 미만으로 우수한 내구성을 가짐을 확인하였다. HCl, HF의 농도와 유속이 증가함에 따라 흡착이 빠르게 일어났으며 유속과 농도에 관계없이 110 min 이후 100% 흡착파과평형이 일어남을 확인할 수 있었다. 또한 SEM Morphology 관찰 결과 점착제가 고르게 분산되어 있고 이온교환수지의 다공구조가 유지되었으며, 흡-탈착 공정에서 성능저하가 없는 것으로 보아 내구성이 있음을 확인하였다.

• 공업화학
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• 제9권6호
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• pp.920-923
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• 1998

본 연구에서는 활성탄소를 산성 및 염기성 용액으로 처리하여 pH변화에 따른 흡착 특성을 비교 분석하였다. 처리하지 않은 일반 활성 탄소와 30 wt. % HCl 및 30 wt. % NaOH 용액으로 처리된 활성탄소의 표면 산도 및 표면 염기도를 Boehm의 선택 중화법을 이용하여 측정하였으며, 그 흡착표면적과 기공도 등은 BET 법을 이용한 $N_2$ 기체 흡착을 통해 알아보았다. 또한 산, 염기 처리된 활성탄소의 흡착 특성을 비교하기 위해 $CO_2$ 및 $NH_3$ 기체의 흡착 실험을 수행하였다. 그 결과 일반 활성탄소와 산성 또는 염기성 용액으로 각각 처리된 활성탄소의 물리적인 표면구조는 큰 변화를 나타내지 않았으나, $CO_2$ 및 $NH_3$에서의 흡착에 있어서 화학적 처리에 따른 서로 다른 표면 관능기에 의하여 상대적으로 향상된 흡착 거동을 나타내었다.

• 대한화학회지
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• 제9권4호
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• pp.185-189
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• 1965

韓國産 酸性白土類 및 silica gel을 aniline yellow, o-nitro aniline, oil orange 色素 benzene 溶液과 작용시켜 非水溶液에서의 色素吸着率을 측정하였다. 그 吸着率은 silica gel이 酸性白土類보다 컸으며 酸性度에는 무관하였다. 또 上記 色素溶液에 각 10%의 添加溶劑 amine, alcohol, halogen類 化合物등을 加하여 高體酸의 色素吸着率의 변화(吸着阻害率)에 대하여 조사한 결과 위에 적은 順으로 그 영향이 적어지고, 同族體에서는 分子量이 적을 수록 그 영향이 커짐을 알았다. 따라서 非水溶液에서의 吸着은 amine基, 水酸基등과 같은 陰性基를 갖는 化合物은 選擇吸着하고 界面張力에 무관계하여 Traulbe系列의 逆轉現象을 나타내었다. 그 逆轉現象(吸着潮害現象)은 그 順位가 添加溶制의 雙極子能率과 대체적으로 일치하는 것으로 보아 固體酸模體인 活性硅酸과 被吸着體사이의 極盛的化學吸着에 의한 것이라 推定된다. 本實驗結果로부터 固體酸의 非水溶液에서의 吸着메카니즘, Traube 系列의 逆轉現象에 관하여 考察하게 되었다.

• 대한화학회지
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• 제36권3호
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• pp.351-359
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• 1992

알칼리 토금속 양이온을 함유하고 있는 Y 제올라이트와 Xe 간의 상호 작용을 이해하기 위하여 Xe의 흡착과 $^{129}Xe$ 핵자기 공명(NMR) 분광법을 이용하였다. 고순도의 NaY 제올라이트 시료를 합성하여 여기에 $Ca^{2+}$와 $Ba^{2+}$를 각각 이온 교환시켜서 CaY와 BaY 제올라이트 시료들을 얻었다. 부피 흡착 실험방법에 따라서 260∼320 K 사이에서 이 시료들의 Xe 흡착 등온선을 측정하였으며 296 K에서 $^{129}Xe$ NMR의 화학적 이동을 측정하였다. 이 시료들에 흡착된 Xe 기체가 제올라이트 표면과 알칼리 토금속 이온들로 구성된 흡착자리들 사이를 매우 빠르게 움직인다고 가정하였을 때 Xe의 화학적 이동을 정량적으로 설명할 수 있었다. 이 결과 알칼리 토금속 이온들이 $Na^+$ 이온이나 제올라이트 골격 표면보다도 Xe을 훨씬 더 강하게 흡착한다는 것을 의미한다. 이 연구에서는 이와 같은 흡착 세기의 차이를 이용하여 Xe 흡착 등온선을 분석하면 Y 제올라이트 수퍼케이지 속에 존재하는 알칼리 토금속 이온의 갯수를 구할 수 있다는 사실을 밝혀내었다.

• 한국환경과학회지
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• 제14권1호
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• pp.61-69
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• 2005

Adsorption characteristics of toluene vapor, which is one of important source of volatile organic compounds (VOCs), by activated carbon were investigated using a fixed bed adsorption column. The operating parameters such as breakthrough curve, adsorption capacity, mass transfer zone (MTZ), and length of unused bed (LUB) were studied. The experimental results showed that the breakthrough time decreased with increasing inlet toluene concentration and gas flow rate. MTZ and LUB increased with the increase of inlet concentration, gas flow rate, and particle size of activated carbon. The adsorption capacity increased with the increase of inlet toluene concentration, while it decreased with increasing particle size. However, it was kept at constant value regardless of the increase of gas flow rate. Adsorption isotherm of toluene vapor could be represented by the Freundlich adsorption equation fairly well. From the adsorption experiments using some VOC gases such as toluene, xylene, butyl acetate. butanol and acetone, it was also found that the adsorption capacity was higher in the case of gas with higher boiling point and lower vapor pressure.