• Korean Chemical Engineering Research
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• 제56권1호
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• pp.14-23
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• 2018

The effect of dodecylbenzene sulfonic acid (DBSA) with different addition amount of DBSA ($M_{DBSA}$), temperatures and solvent-to-oil ratio (SOR, v/v) on asphaltene aggregation in a solvent deasphalting system was investigated. Increasing the $M_{DBSA}$ at SOR 10 and $55^{\circ}C$ caused the asphaltene removal ratio (ARR) to increase first, then maximize at 1 wt% of $M_{DBSA}$ and then decrease continuously. Based on the SARA (saturate, aromatic, resin, asphaltene) composition, the adsorption amount of DBSA on the asphaltene surface and the self-aggregation of the DBSA, the reason for the change in ARR with $M_{DBSA}$ was found due to the adsorption mechanism. In addition, the asphaltene-resin-DBSA colloidal size confirmed the change of adsorption behavior between the asphaltene and DBSA. Based on the results of this study, a hypothetical adsorption mechanism of DBSA on asphaltene aggregation in the solvent deasphalting system was conceived of and proposed.

• Membrane and Water Treatment
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• 제9권2호
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• pp.95-104
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• 2018

Copper pollution around the world has caused serious public health problems recently. The heavy metal adsorption on traditional membranes from wastewater is limited by material properties. Different adsorptive materials are embedded in the membrane matrix and act as the adsorbent for the heavy metal. The carbonized leaf powder has been proven as an effective adsorbent material in removing aqueous Cu(II) because of its relative high specific surface area and inherent beneficial groups such as amine, carboxyl and phosphate after carbonization process. Factors affecting the adsorption of Cu(II) include: adsorbent dosage, initial Cu(II) concentration, solution pH, temperature and duration. The kinetics data fit well with the pseudo-first order kinetics and the pseudo-second order kinetics model. The thermodynamic behavior reveals the endothermic and spontaneous nature of the adsorption. The adsorption isotherm curve fits Sips model well, and the adsorption capacity was determined at 61.77 mg/g. Based on D-R model, the adsorption was predominated by the form of physical adsorption under lower temperatures, while the increased temperature motivated the form of chemical adsorption such as ion-exchange reaction. According to the analysis towards the mechanism, the chemical adsorption process occurs mainly among amine, carbonate, phosphate and copper ions or other surface adsorption. This hypothesis is confirmed by FT-IR test and XRD spectra as well as the predicted parameters calculated based on D-R model.

• Bulletin of the Korean Chemical Society
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• 제18권3호
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• pp.300-305
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• 1997

Effect of a nonionic surfactant, Tween 20 on the adsorption and kinetic mechanism for the hydrolysis of a microcrystalline cellulose, Avicel PH 101, by endoglucanase Ⅰ (Endo Ⅰ) and exoglucanase Ⅱ (Exo Ⅱ) isolated from Trichoderma viride were studied. The Langmuir isotherm parameters, amount of maximum adsorption (Amax) and adsorption equilibrium constant (Kad) for the adsorption, were obtained in the presence and the absence of nonionic surfactant. On the addition of Tween 20, the Kad and Amax values of Exo Ⅱ were decreased, while those of Endo Ⅰ were not affected. These indicate that the adsorption affinity of Exo Ⅱ on the cellulose is weakened by nonionic surfactant, and the surfactant enhanced desorption of Exo Ⅱ from insoluble substrate. The enzymatic hydrolysis of the cellulose can be described by two parallel pseudo-first order reactions using the percentages of easily (Ca) and hardly (Cb) hydrolyzable cellulose in Avicel PH 101 and associated rate constants (ka and kb). The Ca value was increased by adding Tween 20 for all enzyme samples (Exo Ⅱ, Endo Ⅰ and their 1:1 mixture) implying that the low-ordered crystalline fraction in the cellulose may be partly dispersed by surfactant. The ka value was not affect by adding Tween 20 for all enzyme samples (Exo Ⅱ, Endo Ⅰ and their 1:1 mixture). The kb value of Exo Ⅱ was increased by adding Tween 20, while that of Endo Ⅰ was not affected. This suggests that the surfactant helps the Exo Ⅱ desorb from microcrystalline cellulose, and increase the hydrolysis rate. These results were show that the increase of hydrolysis of cellulose by the nonionic surfactant is due to both the activation of Exo Ⅱ and partial defibrillation of the cellulose.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2001년도 총회 및 춘계학술발표회
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• pp.168-171
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• 2001

Organobentonite modified with hexadecyltrimethylammonium (HDTMA) was used to quantify an adsorption of heavy metals. Based on preliminary experiments, optimal soil/solution ratio, a range of pH, and electrolyte were selected. Adsorption experiments of cadmium and lead were conducted to quantify an adsorption selectivity to bentonite and organobentonite. Adsorption of cadmium and lead to bentonite was increased with increasing a soil/solution ratio. Adsorption of cadmium and lead to bentonite was increased with increasing a soil/solution ratio. Adsorptions of heavy metal to organobentonite were slightly reduced relative to bentonite. This study used the principle of hard-soft-acid-base (HBAB) to interpretate an adsorption mechanism. Because of competition between cadmium and lead. adsorption of cadmium and lead was reduced in mixture of heavy metals. Adsorption selectivity.

• 상하수도학회지
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• 제23권1호
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• pp.113-119
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• 2009

The feasibility of using cork oak bark for phosphorus removal from wastewater was evaluated in this study. Recently, development of more cost-effective media while maintaining high efficiency in pollutants removal has received concern. Barks have a negative surface charge and, hence, tend to show a high affinity to bind cations, and they need to undergo chemical modification to increase their adsorption capacity of anions. Bark was hydrolyzed by HCl solution and it received modification using an aqueous solution of high molecular weight polyethylenimine(PEI). Surface modification with HCl and PEI resulted in a decrease of specific surface area of the bark from $1.932 m^2/g$ to $1.094 m^2/g$. The adsorption experiments were carried out in batch tests and the data were fitted to the Langmuir isotherm and Freundlich isotherm equations. Phosphate removal rate was higher at the lower solution pH possibly due to the form of phosphate ion in solution. For the initial phosphate concentration of 10 mg/L, maximum adsorption was 20.88 mg P/g at pH 3 and 12.02 mg P/g at pH 5. Mechanism of phosphorus sorption onto the HCl-PEI bark was examined through FT-IR spectrometer. Ion exchange between $NH^+$ and $H_2PO_4{^-}$ appeared to be a key mechanism of phosphate adsorption onto the HCl-PEI bark surface.

• 한국토양비료학회지
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• 제29권2호
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• pp.107-112
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• 1996

토양의 규산 흡착기작을 밝히고자 continuous stirred-flow(연속진탕흘림) 법을 이용하여 시간 경과에 따른 규산 흡착량 변화에 대한 실험을 $25^{\circ}C$, pH 3수준(5, 6.5, 8)에서 실시하였다. 규산 흡착량은 실험기간내 최대 흡착량을 보이지 않고 계속 증가 하였다. 시간에 따른 규산의 흡착과정을 2단계로 구분 하였고, 1단계 반응과정은 아래의 지수함수식에서 고도의 유의성있는 상관관계를 보였다 $$R_{ad}=K_a*(Q_{OH}^S)^n$$ 여기서 $R_{ad}$는 규산흡착속도($Si\;{\mu}mal/min$), $Q_{OH}^S$는 알칼리 투여를 통하여 생성된 토양표면 음전하량, $K_a$와 n 은 상수이다. 1단계 반응과정의 n값은 1.1로 한자리 결합(monolantate ligand bonding)에 의한 흡착과정인 것으로 나타났다. 2단계 과정은 아래 식에서 고도의 유의성있는 상관관계를 보였다. $$R_{ad}=K_b*(pH)$$ 이때 $K_b$ 는 비례상수로, pH 증가에 따른 규산 흡착 속도의 증가 추세가 지수 함수적으로 감소하는 경향을 보였다.

• 한국토양비료학회지
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• 제28권2호
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• pp.105-113
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• 1995

토양(土壤)의 구성성분(構成成分) 중 많은 부분(部分)을 차지하고 있는 철(鐵) 및 알루미늄의 수산화물(水酸化物)에 의한 중금속(重金屬)ion들의 흡착(吸着) mechanism을 구명(究明)하기 위하여, 무정형(無晶型) Fe 및 Al 수산화물(水酸化物), Goethite 및 Gibbsite에 의한 중금속(重金屬)ion들의 흡착(吸着) mechanism을 조사(調査)하였다. 1. 철(鐵) 및 알루미늄의 수산화물(水酸化物)에 의한 중금속(重金屬)ion들의 흡착등온선(吸着等溫線)은 Langmuir식(式)에 잘 부합되었으며, 이들의 최대흡착량(最大吸着量) 및 흡착(吸着)에너지는 무정형(無晶型) 수산화물(水酸化物)이 결정형(結晶型) 수산화물(水酸化物)보다 또 알루미늄 수산화물(水酸化物)이 철수산화물(鐵水酸化物)보다 많았다. 2. 중금속(重金屬)ion별(別) 최대흡착량(最大吸着量) 및 흡착(吸着)에너지는 Cu>Zn>Cd의 순(順)으로 CEC, 비표면적(比表面積) 및 하전밀도(荷電密度)와 정(正)의 상관(相關)이 인정(認定)되었다. 3. Goethite 및 Gibbsite에 의한 중금속(重金屬)ion들의 첫번째 흡착(吸着) mechanism은 $Cl^-$를 수반하는 nonspecific adsorption으로 1 Mole의 중금속(重金屬)ion이 흡착(吸着)되는데 대하여 표면(表面) aquo group이나 hydroxo group으로 부터 1 Mole의 H가 탈착(脫着)되었으며, 회응비율(灰應比率)은 pH가 증가(增加)할수록 감소(減少)되고 흡착(吸着)된 중금속(重金屬)ion들은 치환성양(置煥性陽)ion에 의하여 재치환(再置換)될 수 있었다. 4. Goethite 및 Gibbsite에 의한 중금속(重金屬)ion들의 두번째 흡착(吸着) mechanism은 $Cl^-$을 수반하지 않는 specific adsorption으로 1 Mole의 중금속(重金屬)ion이 흡착(吸着)되는데 대하여 표면(表面) aquo group이나 hydroxo group으로부터 2 Mole의 $H^+$가 탈착(脫着)되었으며. 흡착반응(吸着反應)의 비율(比率)은 pH가 증가(增加)할수록 증가(增加)되었으며 흡착(吸着)된 중금속(重金屬)들은 置換性 陽ion에 의하여 再置煥되지 않았다.

• 상하수도학회지
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• 제11권4호
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• pp.110-117
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• 1997

Performances of combined adsorption and coagulation were evaluated as one of the options for pre-treatment or post-treatment of MSW landfills leachate and industrial landfill leachate. The COD and color removals of leachate from an old MSW landfill were 35% and 33% at an alum dose of 300mg/L with preceding PAC(powdered activated carbon) dose of 200mg/L, respectively. The COD and color removals of leachate from an young MSW landfill were 58% and 25% at an alum dose of 700mg/L and PAC dose of 500mg/L, respectively. The COD and color of biologically treated leachate from an industrial waste landfill were removed up to 32% and 68%, respectively, with pH control at addition of 500mgAlum/L and 1,000mgPAC/L. Adsorption and coagulation process with pH control showed better COD and color removals than the process without pH control for biologically treated leachate from an industrial waste landfill. The color removal was influenced greatly by pH control, while COD removal was not significant. No difference in removal efficiency was observed between adsorption-coagulation and coagulation-adsorption process. The COD removal was accomplished mainly by adsorption, while coagulation was a key mechanism of color removal. However, the mechanism of COD removal was obscure, when BOD/COD ratio was high. Maximum net increases in COD and color removals by the adsorption-coagulation process were respectively 45% and 46% compared with the unit process of adsorption or coagulation, although those removals depended on leachate characteristics. Thus, adsorption-coagulation process was considered to be effective for pre- and post-treatment of landfill leachate, and has distinct features of simple, flexible, stable and reliable operation against fluctuation leachate quality and flowrate.

• Nuclear Engineering and Technology
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• 제52권10호
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• pp.2394-2401
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• 2020

Octadecylamine is an effective film-forming amine that protects carbon steel from corrosion. In the present study, the effect of octadecylamine concentration on adsorption on a carbon steel surface was investigated in anaerobic alkaline solution by using SEM/EDS, TEM and the Materials Studio simulation techniques. TEM morphology observation and EDS elemental detection determine the thicknesses of octadecylamine film on a carbon steel surface, which are confirmed by the in-situ electrochemical impedance spectroscopy measurement and resistance calculation. The Materials Studio simulation reveals the number of octadecylamine film layers at different concentrations. Results obtained in this study indicate that adsorption of octadecylamine film on carbon steel proceeds with the multi-layer adsorption mechanism.

• 한국진공학회지
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• 제17권6호
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• pp.549-554
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• 2008

수소 플라즈마 처리된 유리 기판에 스핀 코팅 시스템을 이용하여 nickel chloride를 코팅하여 단백질칩 플레이트를 제조하였다. 다양한 플라즈마 처리 시간대에서 histidine tagged 단백질의 부착 능력 특성을 연구하였다. 유리 기판 표면에서 nickel chloride와 단백질 특성을 particle size analysis를 이용하여 관찰하였고, 단백질의 부착 능력 정도를 bio imaging analyzer system으로 측정하였다. 실험 결과에 따르면, 플라즈마 처리 시간이 증가할수록 단백질 부착 능력은 감소하는 것으로 나타났다. 기판 표면에서의 단백질 부착능력 특성에 관한 mechanism은 본문의 결과 및 토의에서 논의되었다. 플라즈마 처리된 단백질칩 기판에 대한 표면 안정화는 바이오센서 시장에서 큰 관심을 끌 것으로 기대된다.