• Proceedings of the Membrane Society of Korea Conference
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• 1995.10a
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• pp.29-30
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• 1995

산업폐수는 종종 희석용액 내에 많은 유독성 물질을 함유하고 있다. 산업폐수를 처리하는 분리공정으로 역삼투막과 한외여과와 같은 막분리 기술은 분리 공정이 간단하고 상변화없이 폐수용량을 크게 감소시킬 수 있고 에너지 소모가 작은 장점을 가지고 있어 그 적용이 확산되고 있다. 계면활성제의 흡착성을 이용한 한외여과 막분리는 높은 막투과속도와 계면활성제의 높은 선택성이 결합된 것인데, Sodium Dodecyl Sulfate(SDS)와 같은 계면활성제를 이용하여 폐수로부터 불용성 중금속 이온과 독성의 유기물질을 분리하는 데에 적용할 수 있다. 임계미셀농도(CMC) 이상에서의 농도에서, 60~200 계면활성제 분자들이 거대분자나 미셀을 형성하면서 서로 응집된다. 그러므로 음으로 하전된 미셀과 결합된 금속 음이온은 2,000에서 10,000 범위의 분자량을 가지는데 역삼투막(RO)보다 작은 압력에서 상당히 큰 막투과속도를 가진 한외여과막에 의해 선택적으로 제거될 수 있다 본 연구의 목적은 중공사 한외여과막의 막투과속도에 미치는 인자들의 영향과, 계면활성제의 흡착성을 이용한 중공사 한외여과 막분리계 성능에 미치는 금속의 형태, S/M 몰비등의 효과를 결정하는데 있다.

• Journal of Korean Society of Environmental Engineers
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• v.35 no.12
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• pp.897-905
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• 2013

In this study, sorption coefficients (${\log}K_{OC}$, n) for the binding of phenanthrene (PHE) to soil humins, insoluble fraction of soil humc substances (HS), were determined and relationship between the sorption coefficients and structural characteristics of the soil humins were investigated. The soil humins used in the present study were isolated from 7 different soils including 5 domestic soils, an IHSS standard and a peat soil, and characterized by elemental analysis and CPMAS $^{13}C$ NMR method. $^{13}C$ NMR spectral features indicate that the soil humins are mainly made up of aliphatic carbons (57.1~72.3% in total carbon) with high alkyl-C moiety, and the alkyl-C contents ($C_{Al-H,C}$, %) was in order of granite soil Hu (26~42%) > volcanic ash soil, HL Hu (23.9%) > Peat Hu (14.0%). The results of correlation study show that a positive relationship ($r^2$ = 0.77, p < 0.05) between organic carbon normalized-sorption coefficients ($K_{OC}$, mL/g) and alkyl-C contents($C_{Al-H,C}$, %), while negative relationship ($r^2$ = (-)0.74, p < 0.05) between Freundlich sorption parameter (n) and H,C-substituted aromatic carbon contents ($C_{Ar-H,C}$, %). The magnitude of $K_{OC}$ values are also negatively well correlated with polarity index (e.g., PI, N + O)/C) ($r^2$ = (-)0.74, p < 0.1). These results suggest that the binding capacity (e.g., $K_{OC}$) for PHE is increased in soil humin molecules having high contents of alkyl-C or lower polarity, and nonlinear sorption for PHE increased as the H,C-substituted aromatic carbon contents ($C_{Ar-H,C}$, %) in the soil humins increased. The PHE sorption characteristics on soil humins are discussed based on the dual reactive mode of sorption model.

• Proceedings of the Korean Vacuum Society Conference
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• 2003.08a
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• pp.42-42
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• 2003

• Clean Technology
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• v.28 no.3
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• pp.249-257
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• 2022

The adsorption equilibria of nitrogen on a region of nanoporous carbonaceous adsorbent with local molecular orientation (LMO) were calculated by grand canonical Monte Carlo simulation at 77.16 K. Regions of LMO of identical size were arranged on a regular lattice with uniform spacing. Microporosity was predominately introduced to the model by removing successive out-of-plane domains from the regions of LMO and tilting pores were generated by tilting the basic structure units. This pore structure is a more realistic model than slit-shaped pores for studying adsorption in nanoporous carbon adsorbents. Their porosities, surface areas, and pore size distributions according to constrained nonlinear optimization were also reported. The adsorption in slit shaped pores was also reported for reference. In the slit shaped pores, a clear hysteresis loop was observed in pores of greater than 5 times the nitrogen molecule size, and in capillary condensation and reverse condensation, evaporation occurred immediately at one pressure. In the LMO pore model, three series of local condensations at the basal slip plane, armchair slip plane and interconnected channel were observed during adsorption at pore sizes greater than about 6 times the nitrogen molecular size. In the hysteresis loop, on the other hand, evaporation occurred at one or two pressures during desorption.

• Clean Technology
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• v.24 no.4
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• pp.348-356
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• 2018

The adsorption equilibria of oxygen, nitrogen and argon on carbonaceous adsorbent with slit-shaped and randomly etched graphite (REG) pores were calculated by molecular simulation method. Reliable models of adsorbents and adsorbates for adsorption equilibria are important for the correct design of industrial adsorptive separation processes. At the smallest physical pore of $5.6{\AA}$, only oxygen molecules were accommodated at the center of the slit-shaped pore, and from $5.9{\AA}$ nitrogen and argon molecules could be accommodated in the pores. Slit pores showed higher adsorption capacity compared with REG pores with same averaged reenterance pore size due to dead volume and inaccessible volume in defected pores. And it was shown the adsorption capacities of oxygen and argon was same in larger pore size. From calculated adsorption isotherms at 298 K it showed that the adsorption capacity ratio of oxygen to nitrogen is increased as pressure is increased.

• Proceedings of the Membrane Society of Korea Conference
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• 1994.03a
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• pp.53-77
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• 1994

기체 분리 방법의 종류 일반적으로 기체를 분리하는 방법에는 다음과 같이 3가지 종류가 있다. Cryogenic Separation (심냉분리법) : 기체를 압축, 냉각, 액화 시킨후 boiling point 차이를 이용한 증류볍으로 분리하는 방법을 말하며 기체 분리 기술중 가장 오래된 기술이다. Adsorption (흡착법) - PSA : 분리 하고자 하는 기체를 흡착제에 흡착 시키고 흡착되지 않는 잔류 기체는 다른 용리에 이송한 후 흡착된 기체를 온도차, 압력차 등을 이용하여 탈착 시키면서 기체를 분리하는 방법이다. Membrane Separation (막분리법) : 특수하게 제작된 막의 한쪽면으로기체 (여러 종류의 기체분자로 구성된 혼합기체)가 접촉되어 막 반대면의 압력이 저압 상태로 될때 혼합기체증의 특정기체가 막을 투과하는 현상을 이용하여 분리하는 방법을 말하며 이때에 투과현상은 막과 친화성이 좋은 특정기체분자가 압력차를 Driving Force로 하여 막의 표면에 용해 되고 이어서 막 내부에서 농도구배에 의한 확산이 일어나고 다른면에서 탈착 되어지는 원리이다.

• Journal of the Korean Chemical Society
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• v.18 no.2
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• pp.79-84
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• 1974

Adsorption isotherms of benzene and its derivatives on Spheron 6, a graphitized carbon black, are obtained using a sensitive quartz beam microbalance. From the isotherms the molecular area of each adsorbate on Spheron 6 is calculated on the basis of nitrogen area of 16.2 $A^2$. the results show that the molecules of each species are adsorbed on Spheron 6 with the planes of benzene rings lying flat on the surfaces and doing hindered rotation.

• The Korean Journal of Food And Nutrition
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• v.13 no.3
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• pp.242-248
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• 2000

수산물 가공시 흘러나오는 폐수 중에 함유되어 있는 수용성 단백질을 chitosan에 흡착시키기 위하여 albumin과 hemoglobin, albumin-myoglobin 혼합단백질을 이용하여 chitosan과의 흡착 및 chitosan 제조조건에 따른 흡착효과와 chitosan의 수용성 단백질 흡착에 미치는 인자를 살펴본 결과는 다음과 같다. Chitosan위 탈아세틸화 조건을 60, 70, 80%로 달리하여, albumin, hemoglobin, albumin-myoglobin 혼합용액에 적용했을때 chitosan의 탈아세틸화도가 높을수록 chitosan과 단백질 사이의 흡착률은 높게 나타났다. 초음파 처리에 의하여 chitosan의 분자량이 작을수록 chitosan과 단백질 사이의 흡착률은 높게 나타났다. pH변화에 따른 chitosan과 수용성 단백질의 흡착률은 albumin 및 albumin-myoglobin 혼합용액에서는 pH 4.0에서, hemoglobin용액에서는 pH 7.0에서 흡착률이 높게 나타났다 chitosan과 수용성단백질과의 흡착에서 반응시간은 albumin및 albumin-myoglobin 혼합용액에서는 4시간, hemoglobin용액에서는 3시간까지 흡착률이 증가하였고, 그 이후의 시간이 경화하여도 흡착률의 증가는 거의 보이지 않았다. 수용성 단백질 용액에 NaCl 농도를 0.1M에서 1.0M로 증가시켜 첨가했을때 염의 농도가 높을수록 chitosan과 단백질 사이의 흡착이 잘 일어나지 않았다.

• Korean Journal of Materials Research
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• v.2 no.4
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• pp.279-284
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• 1992

Oxygen adsorption on the single crystal NbC(111) surface was studied by high-resolution electron energy loss and ultraviolet photoelectron spectroscopy. On the NbC(111) surface, oxygen molecules as well as oxygen atoms were adsorbed. Oxygen atoms were located at the 3-fold hollow site of the NbC(111) surface with the frequency of 548c$m^{-1}$. It was found that oxygen molecules had vibrational frequency of 968c$m^{-1}$which was much lower than that of the free oxygen molecule. Also the work function of the NbC(111) surface has increased by adsorption of oxygen molecule. These suggest electron tranfer from the NbC(111) substrate to the 2p${pi}_g$ substrate of the oxygen molecule.

• Journal of the Korean Society of Food Science and Nutrition
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• v.37 no.10
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• pp.1271-1277
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• 2008

Competitive displacement of methylcellulose (MC) absorbed at the oil-water interface was investigated by interfacial composition, surface shear viscosity, or surface tension measurements. It was found that all emulsifiers could competitively displace the interfacial MC from the oil-water interface but their behaviors were different from each other. With Tween 20 added to MC emulsion (1 wt% MC, 10 wt% n-tetradecane, 20 mM bis-tris, pH 7), MC load was steadily decreased with increasing concentrations of the emulsifier, as confirmed by surface shear viscosity measurements; moreover, there was complete MC displacement from the emulsion droplet surface at high concentration (0.1 wt%). The oil-soluble Span 80 was found to show a synergism with MC at the interface, which resulted in higher MC load at relatively low emulsifier concentrations ($\leq$0.05 wt%). At a higher emulsifier concentration (0.1 wt%) limited MC displacement was observed. These results were well supported by surface shear viscosity measurements. With water-soluble SDS, MC load was decreased with increasing concentrations of the emulsifier. Unlike Tween 20, however, it was found that at high concentrations (> 0.1 wt%), there was still some MC remaining at the droplet surface. Surface tension measurements are suggestive of an interfacial complex between MC and SDS.