• 대한화학회지
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• 제21권5호
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• pp.353-361
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• 1977

多分子層 物理吸着에 있어서 第二分子層이나 또는 그 以上의 分子層이 形成될 때에는 分子들은 바로 아래 層의 分子들이 이루는 三角形 또는 四角形 配列의 中心部위에 吸着될 것이라는 前提下에 새로운 物理吸着理論을 提案하고 이 때의 吸着等溫式을 誘導하였다. 誘導된 吸着等溫式에는 monolayer capacity를 나타내는 $v_m$, 第二層 以上의 層에 대한 分子分配函數와 첫째層 分子의 그것間의 比를 나타내는 q/$q_1$ 및 吸着된 分子들의 쌓이는 樣相을 나타내는 n이란 3개의 調節可能한 파라미터가 들어있다. 誘導된 吸着等溫式을 argon이 "Carbolac" carbon 상에 吸着되는 경우와 nitrogen이 Linde silica 상에 吸着되는 경우에 適用시켜 보면 p/$p_0$가 0.8에 이를때까지 理論値와 實驗値가 잘 一致함을 볼 수 있다. 이 두 경우에 있어서 n = 3이라 놓으면 理論値와 實驗値가 가장 잘 一致하므로 이로부터 吸着된 分子들이 아마도 密集方式으로 쌓이게 되는 것이라 結論지울 수 있다.

• 한국산업융합학회 논문집
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• 제6권3호
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• pp.201-205
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• 2003

The effects of adsorption and desorption of alkali-metals on Si(111) surface were investigated by using AES and RHEED-system. The adsorption system is a fundamental interest because of its unique electronic properties such as measurement of work function change, adatom-core level shift. It was found that the growth node of K on Si(111) surface was layer by layer growth and the saturation coverage was 2.0ML at room temperature. Superstructure changes on Si(111) surface according to the alkali-metal thickness and substrate temperatures were accurately defined. By applying the isothermal desorption method, the desorption energies of Li/Si(111) and K/Si(111) surfaces was measured. On Li/Si(111) and K/Si(111) surfaces, the desorption energies were 3.07 eV, 2.19 eV respectively.

• 대한화학회지
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• 제17권2호
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• pp.80-84
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• 1973

고체-액체 경계 면에서의 흡착은 흡착 층을 단일 분자층으로 생각하고 흡착체에 평행한 방향에 대해서는 이차원 액체로 수직한 방향에 대해서는 조화 단진동을 하는 것으로 보고 여기에 천이상태이론을 적용하여 흡착 층에서의 용액의 상태 합을 구성하고, 시클로헥산-벤젠 이성분 용액의 실리카-겔에 대한 흡착에 적용하여, 흡착량과 흡착 층에서의 몰 엔트로피 및 흡착열의 값을 계산하여 얻었다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제44회 동계 정기학술대회 초록집
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• pp.268-268
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• 2013

Water molecules on a Ru(0001) surface are anomalously acidic compared to bulk water. The observation was made by conducting reactive ion scattering, reflection absorption infrared spectroscopy, and temperature-programmed desorption measurements for the adsorption of ammonia onto a water layer formed on Ru(0001). The study shows that the water molecules in the first intact $H_2O$ bilayer spontaneously release a proton to NH3 adsorbates to produce $NH_4{^+}$. However, such proton transfer does not occur for $H_2O$, OH, and H in a mixed adsorption layer or for $H_2O$ in a thick ice film surface.

• 한국정보디스플레이학회:학술대회논문집
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• 한국정보디스플레이학회 2007년도 7th International Meeting on Information Display 제7권1호
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• pp.571-573
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• 2007

It is known that the main source of the area image sticking is the ion charge adsorption on the alignment layer. We found out that the adsorption of the ion charge of the liquid crystal in the cell was physisorption, which takes place between all molecules on any surface providing the adsorption force is small.

• Carbon letters
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• 제10권4호
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• pp.305-313
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• 2009

In this study, the adsorption of toxic pollutants onto cetyltrimethylammonium kaolin (CTAB-Kaolin) is investigated. The organo-kaolin is synthesized by exchanging cetyltrimethylammonium cations (CTAB) with inorganic ions on the surface of kaolin. The chemical analysis, the structural and textural properties of kaolin and CTAB-kaolin were investigated using elemental analysis, FTIR, SEM and adsorption of nitrogen at $-196^{\circ}C$. The kinetic adsorption and adsorption capacity of the organo-kaolin towards o-xylene, phenol and Cu(II) ion from aqueous solution was investigated. The kinetic adsorption data of o-xylene, phenol and Cu(II) are in agreement with a second order model. The equilibrium adsorption data were found to fit Langmuir equation. The uptake of o-xylene and phenol from their aqueous solution by kaolin, CTAB-kaolin and activated carbon proceed via physisorption. The removal of Cu(II) ion from water depends on the surface properties of the adsorbent. Onto kaolin, the Cu(II) ions are adsorbed through cation exchange with $Na^+$. For CTAB-kaolin, Cu(II) ions are mainly adsorbed via electrostatic attraction with the counter ions in the electric double layer ($Br^-$), via ion pairing, Cu(II) ions removal by the activated carbon is probably related to the carbon-oxygen groups particularly those of acid type. The adsorption capacities of CTAB-kaolin for the investigated adsorbates are considerably higher compared with those of unmodified kaolin. However, the adsorption capacities of the activated carbons are by far higher than those determined for CTAB-kaolin.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2000년도 추계학술대회
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• pp.196-201
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• 2000

The influence of adsorption on cadmium toxicity to soil microorganisms in smectite-rich soils and sediments was quantified as a function of solution and sorbent characteristics. Adsorption and surface complexation experiments were conducted to infer Cd sorption mechanisms to a reference smectite and three fractions of a Veritsol soil, and to elucidate the effects of the surface complexation on Cd bioavailability and toxicity in soils and sediments. Cadmium adsorption isotherms conformed to the Langmuir adsorption model, with adsorptive capacities of the different samples dependent on their characteristics. Equilibrium geochemical modeling (MINTEQA2) was used to predict the speciation of Cd in the soil suspensions using Langmuir and Triple Layer surface complexation models. The influence of adsorption and surface complexation on cadmium toxicity to soil microorganisms was assessed indirectly through the relative change in microbial hydrolysis of fluorescein diacetate (FDA) as a function of total Cd concentration and sorbent characteristics. Adsorption decreased the toxicity of Cd to soil microorganisms. Inner-sphere complexation is more effective than outer-sphere complexation in reducing the bioavailability and toxicity of heavy metals in soils and sediments.

• Bulletin of the Korean Chemical Society
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• 제3권2호
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• pp.37-44
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• 1982

In this work we have studied the multilayer stepwise adsorption of gases on solid adsorbents based on the previously developed theory. It is shown that stepwise adsorption isotherms emerge from our theory if an ad hoc adsorption regarding the degree of occupation for each successive layer is abolished and the effect of lateral intermolecular interactions among adsorbate molecules is included. In addition to these the effect of vertical interactions has also been taken into consideration. It seems that the vertical interaction plays a role in deciding the shape and the position of steps in resulting isotherms. It is evident from this research that it is the lateral interaction that is responsible for stepwise adsorption as long as the adsorbent surface is uniform and temperature is sufficiently low.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2011년도 제41회 하계 정기 학술대회 초록집
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• pp.197-197
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• 2011

In this study, in contrast with cases in which Scanning Tunneling Microscopy (STM) tip-induced reactions were instigated by the tunneling electrons, the local electric field, or the mechanical force between a tip and a surface, we found that the tungsten oxide (WO3) covered tungsten (W) tip of a STM acted as a chemical catalyst for the S-H dissociative adsorption of phenylthiol and 1-octanethiol onto a Ge(100) surface. By varying the distance between the tip and the surface, the degree of the tip-catalyzed adsorption could be controlled. We have found that the thiol head-group is the critical functional group for this catalysis and the catalytic material is the WO3 layer of the tip. After removing the WO3 layer by field emission treatment, the catalytic activity of the tip has been lost. 3-mercapto isobutyric acid is a chiral bi-functional molecule which has two functional groups, carboxylic acid group and thiol group, at each end. 3-Mercapto Isobutyric Acid adsorbs at Ge(100) surface only through carboxylic acid group at room temperature and this adsorption was enhanced by the tunneling electrons between a STM tip and the surface. Using this enhancement, it is possible to make thiol group-terminated surface where we desire. On the other hand, surprisingly, the WO3 covered W tip of STM was found to act as a chemical catalyst to catalyze the adsorption of 3-mercapto isobutyric acid through thiol group at Ge(100) surface. Using this catalysis, it is possible to make carboxylic acid group-terminated surface where we want. This functional group-selective adsorption of bi-functional molecule using the catalysis may be used in positive lithographic methods to produce semiconductor substrate which is terminated by desired functional groups.

• 공업화학
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• 제24권1호
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• pp.24-30
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• 2013

Quartz crystal microbalance with dissipation monitoring (QCM-D)을 활용하여 양이온성으로 치환된 전분 및 올리고당의 흡착특성을 연구하였다. 전 합성계열의 흡착량은 양이온 계면활성제($C_{12{\sim}16}$ trimethylammonium bromide) 대비 높은 흡착량을 보였으며, 치환비율 및 분자량에 따른 특별한 흡착량의 경향성은 관찰되지 않았다. 반면에, 점탄성(viscoelasticity) 측면에서는 분자량이 증가될수록 흡착층의 강도가 증가되는 경향이 관찰되었다. 흡착 및 탈착실험에서 단분자인 양이온성 계면활성제의 흡착량의 차이는 약 4~9배에 수준의 큰 차이가 발생되었으나 양성치환된 전분계열에서는 0~50% 수준의 작은 차이를 나타내었다. 또한, 탈착단계 이후 흡착단계에 비해 양이온 계면활성제에서는 흡착층의 강도 (rigidity)가 감소된 반면 양성치환된 전분계열에서는 강도가 증가되는 상반된 경향이 관찰되었다.