• Korean Chemical Engineering Research
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• 제48권6호
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• pp.768-775
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• 2010

제올라이트(faujasite) 흡착제가 충진된 흡착탑에서 에탄/에틸렌 혼합가스의 흡착 동특성과 탈착제로 프로판을 이용한 치환탈착 시의 동특성을 실험 및 이론적으로 연구하였다. 물질수지와 에너지수지를 고려하고 다성분 흡착평형으로 이상흡착상 모델을 적용한 전산모사는 흡탈착 파과곡선 실험 결과를 잘 예측하였다. 흡착파과 시 에탄의 롤-엎은 흡착압력이 높고, 온도가 낮을수록 증가하였다. 에탄/에틸렌 혼합가스로 포화된 흡착탑으로 탈착제인 프로판을 주입하여 치환탈착할 때 탈착단계의 일정 시간 동안에 거의 100%에 가까운 에틸렌을 얻을 수 있었다. 탈착제의 흡착세기는 에틸렌의 탈착 및 재흡착 시에 큰 영향을 미치는 것으로 나타났다. 프로판 대신 흡착세기가 강한 이소부탄을 탈착제로 사용한 경우에 탈착단계 후 재흡착에서 에틸렌 흡착용량이 많이 감소하는 현상이 관찰되었다. 전산모사를 통하여 ${(q_s{\times}b)}_{C_2H_4}/{(q_s{\times}b)}_{C_3H_s}$의 비율이 0.83일 때, 즉 탈착제와 에틸렌이 거의 유사한 정도의 흡착세기를 가질 때 치환탈착공정의 성능이 우수하였다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2012년도 제42회 동계 정기 학술대회 초록집
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• pp.268-268
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• 2012

Adsorption and desorption of toluene from bare and $TiO_2$-coated silica with a mean pore size of 15 nm was studied using breakthrough curves and temperature programmed desorption. Thicknesses of $TiO_2$ films prepared by atomic layer deposition on silica were < 2 nm, and ~ 5 nm, respectively. For toluene adsorption, both dry and humid conditions were used. $TiO_2$-thin film significantly improved toluene adsorption capacity of silica under dry condition, whereas desorption of toluene from the surface as a consequence of displacement by water vapor was more pronounced for $TiO_2$-coated samples with respect to the result of bare ones. In the TPD experiments, silica with a thinner $TiO_2$ film (thickness < 2 nm) showed the highest reactivity for toluene oxidation to $CO_2$ in the absence and presence of water. We show that the toluene adsorption and oxidation reactivity of silica can be controlled by varying thickness of $TiO_2$ thin films.

• 대한토목학회논문집
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• 제13권2호
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• pp.279-285
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• 1993

여러 오염물질 사이의 흡착 경쟁, 평형, 물질확산의 상호 연관성을 이해하는 것은 효율적인 활성탄 흡착탑 설계 및 운전을 위하여 중요하다. 흡착탑내에서의 오염물질의 확산 및 흡착 현상을 동역학적 및 수학적으로 예측하기 위하여 "Micro-Diameter-Depth Adsorption System" Technique을 개발하여 평형 및 물질확산 계수들을 측정하였다. 활성탄 입자의 외부 "Film Transfer"와 입자 내부에서의 "Surface Diffusion"을 고려한 오염 물질 사이의 흡착경쟁, 탈착, Chromatographic Displacement Effect 등을 Homogeneous Surface Diffusion Model(HSDM)을 이용하여 예측했다. p-Chlorophenol(PCP)/p-Nitrophenol(PNP)의 Breakthrough Curve에서 PCP는 PNP에 의해 Displace되는 현상을 볼 수 있었으며 HSDM은 이를 잘 예측하였다. Dodecylbenzenesulfonate (DBS)는 흡착된 DBS의 일부분이 비가역적 흡착반응을 보인다는 가정하에서 HSDM에 의해 잘 예측될 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제23권2호
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• pp.205-214
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• 2002

The reaction of gas-phase atomic hydrogen with hydrogen atoms chemisorbed on a silicon surface is studied by use of the classical trajectory approach. Especially, we have focused on the mechanism changes with the hydrogen surface coverage difference. On the sparsely covered surface, the gas atom interacts with the preadsorbed hydrogen atom and adjacent bare surface sites. In this case, it is shown that the chemisorption of H(g) is of major importance. Nearly all of the chemisorption events accompany the desorption of H(ad), i.e., adisplacement reaction. Although much less important than the displacement reaction, the formation of $H_2(g)$ is the second most significant reaction pathway. At gas temperature of 1800 K and surface temperature of 300 K, the probabilities of these two reactions are 0.750 and 0.065, respectively. The adsorption of H(g) without dissociating H(ad) is found to be negligible. In the reaction pathway forming $H_2$, most of the reaction energy is carried by $H_2(g)$. Although the majority of $H_2(g)$ molecules are produced in sub-picosecond, direct-mode collisions, there is a small amount of $H_2(g)$ produced in multiple impact collisions, which is characteristic of complex-mode collisions. On the fully covered surface, it has been shown that the formation of $H_2(g)$ is of major importance. All reactive events occur on a subpicosecond scale, following the Eley-Rideal mechanism. At gas temperature of 1800 K and surface temperature of 300 K, the probability of the $H_2(g)$ formation reaction is 0.082. In this case, neither the gas atom trapping nor the displacement reaction has been found.

• Corrosion Science and Technology
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• 제18권5호
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• pp.155-167
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• 2019

In this study, two novel Schiff base compounds including (3-(4-Chlorophenyl isoxazole-5-yl) methanol and (3-(2,4 dichlorophenol isoxazole-5-yl) methanol as corrosion inhibitors for mild steel in 1 M hydrochloric acid solution were investigated by potentiodynamic polarization, electrochemical impedance spectroscopy (EIS), and density functional theory (DFT) computations. The results showed that the corrosion inhibition efficiency (IE) is remarkably enhanced with the growing concentration of the Schiff base inhibitors. The results from Tafel polarization and EIS methods showed that IE decreases with gradual increments of temperature. This process can be attributed to the displacement of the adsorption/desorption balance and hence to the diminution of the level of a surface coating. Also, the adsorption of two inhibitors over mild steel followed the Langmuir adsorption isotherm. Too, the results of the scanning electron microscope (SEM) images showed that the Schiff base inhibitors form an excellent protective film over mild steel and verified the results by electrochemical techniques. Additionally, the results from the experimental and those from DFT computations are in excellent accordance.

• 한국토양비료학회지
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• 제44권1호
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• pp.15-21
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• 2011

Transport of heavy metals such as Cd is affected by several rate-limiting processes including adsorption and desorption by exchange reactions in soils. In this study, column transport and batch kinetic experiments were performed to assess Cd mobility in a double-layered soil with a reclaimed saline and sodic soil (SSS) as top soil and macroporous granule (MPG) as a bottom layer. For individual soil layer having different physical and chemical properties, Cd was considered to be nonlinear reactivity with the soil matrix in layered soils. The dispersive equation for reactive solutes was solved with three types of boundary conditions for the interface between soil layers. The adsorption of Cd with respect to the saline-sodic sandy loam and the MPG indicated that the nature of the sites or the mechanisms involved in the sorption process of Cd was different and the amounts of Cd for both of samples increases with increasing amounts of equilibrium concentration whereas the amount of Cd adsorbed in saline-sodic sandy loam soil was higher than that in MPG. The results of breakthrough curve indicating relative Cd retardation accompanied by layer material and sequence during leaching showed that the number of pore volumes to reach the maximum relative concentration of 1 increased in the order of MPG, SSS, and double layer of SSS-MPG. Breakthrough curves (BTCs) from column experiments were well predicted with our double-layered model where independently derived solute physical and retention parameters were implemented.