• 한국염색가공학회지
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• 제19권3호
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• pp.26-36
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• 2007

This study was carried out to treat the aqueous solutions containing reactive dyes(RB19, RR120 and RY179) by the Ozone demand flask method and adsorption process using activated carbon fiber(ACF) which are one of the main pollutants in dye wastewater. Ozone oxidation of three kinds of the reactive dyes was examined to investigate the reactivity of dyes with ozone, competition reaction and ozone utilization on various conditions for single- and multi-solute dye solution. Concentration of dyes was decreased continuously with increasing ozone dosage in the single-solute dye solutions. Competition quotient values were calculated to investigate the preferential oxidation of individual dyes in multi-solute dye solutions. Competition quotients(CQi) and values of the overall utilization efficiency, ${\eta}O_3$, were increased at 40mg/l of ozone dosage in multi-solute dye solutions. ACF(A-15) has much larger specific surface area$(1,584m^2/g-ACF)$ in comparison with granular activated carbon adsorbent (F400, $1,125m^2/g-GAC$), which is commonly used, and most of pores were found to be micropores with pore radius of 2nm and below. It was found that RB19 was most easily adsorbed among the dyes in this study. In the case of PCP (p-chlorophenol) and sucrose, which are single component adsorbate, adsorption capacities of ACF(A-15) were in good agreement with the batch adsorption measurement, and saturation time predicted of ACF columns for these components was also well agreed with practically measured time. But in the case of reactive dyes, which have relatively high molecular weight and aggregated with multi-components, adsorption capacities or saturation time predicted were not agreed with practically measured values.

• 대한환경공학회지
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• 제22권12호
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• pp.2215-2226
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• 2000

수중에서 친수성을 나타내는 부유물질의 안정성에 대한 계면활성제의 영향을 고찰하기 위해 quartz에 대한 잔세이트 homologs의 흡착양상을 FT-IR spectroscopy를 통해 조사함으로써 흡착반응 메카니즘을 규명하고자 하였다. 그리고, 이의 결과를 동일 조건에서의 접촉각의 측정 결과와 비교고찰함으로써 반응 메카니즘 해석에 대한 신뢰성을 부여하였다. 에틸 잔세이트의 경우 흡착시간에 따라 quartz 표면에 monolayer를 형성한 후에 계속하여 reverse orientation을 통한 흡착이 진행되어 double layer가 형성됨이 관찰되었다. 프로필과 부틸 잔세이트의 경우에도 유사한 경향이 나타났는데, alkyl group의 C분자수가 증가함에 따라 흡착시간은 감소됨이 파악되었다. Young's equation을 통한 흡착반응의 열역학적 관점에 대해 논하였으며, 동일한 잔세이트의 경우 농도 변화에 따른 흡착속도의 변화에 대해서도 관찰하였다. 본 연구를 통해 수계에서 계면활성제가 부유성 물질에 작용하는 양상은 계면활성제의 농도와 분자구조, 그리고 수중에서 이 물질이 잔류하는 시간에 따라 크게 영향을 받음을 알 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제30권8호
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• pp.1755-1759
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• 2009

Surface structure and molecular orientation of self-assembled monolayers (SAMs) formed by the spontaneous adsorption of tetrahydrothiophene (THT) and thiophene (TP) on Au(111) were investigated by means of scanning tunneling microscopy (STM) and carbon K-edge near edge X-ray absorption fine structure (NEXAFS) spectroscopy. STM imaging revealed that THT SAMs have a commensurate (3 ${\times}\;2\sqrt[]{3}$) structure containing structural defects in ordered domains, whereas TP SAMs are composed of randomly adsorbed domains and paired molecular row domains that can be described as an incommensurate packing structure. The NEXAFS spectroscopy study showed that the average tilt angle of the aliphatic THT ring and $\pi$-conjugated TP ring in the SAMs were calculated to be about $30^o\;and\;40^o$, respectively, from the surface normal. It was also observed that the $\pi$* transition peak in the NEXAFS spectrum of the TP SAMs is very weak, suggesting that a strong interaction between $\pi$-electrons and the Au surface arises during the self-assembly of TP molecules. In this study, we have clearly demonstrated that the surface structure and adsorption orientation of organic SAMs on Au(111) are strongly influenced by whether the cyclic ring is saturated or unsaturated.

• 한국환경보건학회지
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• 제29권3호
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• pp.50-58
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• 2003

Removal of heavy metal ions (Cd$^{2+}$, Cr$^{3+}$, Cu$^{2+}$, Pb$^{2+}$) by several chitosans was studied and the molecular weight of chitosan was investigated in order to examine the effect of autoclaving. Chitosan were divided into 3 groups (A type, controlled chitosan; B type, autoclaved for 15 min; C type, autoclaved for 60 min). The heavy metal removal capacity and rate of B type chitosan were higher than those of A type and B type chitosan. The molecular weight of chitosan was decreased by the increase of autoclaving time. Therefore, the heavy metal capacity was not well correlated to the molecular weight. Freundlich and Langmuir isotherm was determined from the experimental results of equilibrium adsorption for individual heavy metal ions on chitosan. Langmuir isotherm was well fitted to this experimental data. The heavy metal removal capacity of B type chitosan was in the order of Pb$^{2+}$ > Cu$^{2+}$ > Cd$^{2+}$> Cr$^{3+}$.3+/.$.3+/.

• 대한화학회지
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• 제22권6호
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• pp.380-385
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• 1978

진공미량저울을 사용하여 Spheron 6 위에서 o-크실렌의 여러 온도에서의 흡착등온곡선을 얻고 이들로 부터 BET 방법을 써서 흡착분자 단면적을 구하였다. 이 단면적의 값은 $-15^{\circ}C$까지에서는 변화가 없었고 -15와 $-14^{\circ}C$ 사이에서 갑자기 변하여 $-14^{\circ}C$ 이상의 온도에서는 다시 일정한 값을 유지하였다. 이 결과는 $-15^{\circ}C$ 보다 낮은 온도에서는 촘촘히 쌓인 편재흡착이 일어나고 $-14^{\circ}C$ 이상의 온도에서는 벤젠고리를 중심으로한 하나의 회전자유도를 얻는 것으로 생각된다.

• Macromolecular Research
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• 제12권4호
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• pp.342-351
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• 2004

Poly(ethylene glycol) (PEG1K) and sulfonated PEG (PEG1K-SO$_3$) methacrylate (MA) copolymers have been prepared and characterized. The structures of the synthesized copolymers were confirmed by $^1$H and $^{13}$ C NMR spectroscopy and elemental analysis. The bulk characteristics of the copolymers were evaluated by viscosity and thermal analysis. The surface properties of the copolymers were investigated using dynamic contact angle measurements and electron spectroscopy for chemical analysis. The hydrophilicity of the surfaces modified with PEG1KMA or PEG1K-SO$_3$MA increased, possibly as a result of the orientation of the hydrophilic PEG1KMA/PEG1K-SO$_3$MA chains into the water phase. Platelets adhered less to the surfaces of the copolymers than they did to a polyurethane control. In addition, adhesion of platelets to the copolymer surfaces decreased upon increasing the chain density of PEG1KMA and sulfonated PEG1KMA in the copolymers. Both bacterial adhesion and protein adsorption were significantly reduced on the copolymer surfaces and their levels differ depending on the kind of surface or media.

• 한국미생물·생명공학회지
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• 제13권3호
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• pp.185-189
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• 1985

L. sporogenes의 배양여액으로부터 균체외 $\beta$-galactosidase를 ammonium sulfate fractionation, Sephadex G-200 gel filtration, DEAE-Sephadex A-50 ion exchange chromatography와 hydroxyapatite adsorption chromatography등의 4단계 정제공정을 거쳐 순수하게 정제하였다. 정제효소는 347배 정제되어 비활성이 1,585 units/mg 이었으며 수율은 39.5%였다. Sephadex G-200 gel filtration에 의한 native enzyme의 분자량은 140,000이고 SDS-PAGE 에 의해서는 분자량이 72,000 한가지로 나타났으므로 L. sporogenes의 $\beta$-galactosidase는 동일한 subunit 2개로 구성된 dimer 효소이다.

• 한국수소및신에너지학회논문집
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• 제15권2호
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• pp.108-118
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• 2004

To find out rational design and synthetic strategies toward efficient hydrogen storage materials, molecular modeling and quantum mechanical studies have been carried out on the MOFs(Metal-Organic Frameworks) having various organic linkers and nanocube frameworks. The calculation results about the free volume ratio, surface area, and electron density variation of the frameworks indicated that the capacity of the hydrogen storage of MOFs was largely dependent on the specific surface area and electron localization around benzene ring rather than the free volume of MOFs. The prediction of the modeling study could be supported by the hydrogen adsorption experiments using IRMOF-1 and -3, which showed more enhanced hydrogen storage capacities of IRMOF-3 compared with the IRMOF-1's at both experimental conditions, 77K, ∠ $H_2$ 1 atm and ambient temperature, ∠ $H_2$ 35 atm.

• 한국물환경학회지
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• 제21권2호
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• pp.205-210
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• 2005

There has been a growing interest in NF membrane for drinking water treatment, because it can remove simultaneously both hardness and hazardous micro pollutants such as pesticides and THM precursors. In this work, a hollow fiber NF membrane known as a composite membrane was employed for the rejection properties of both hydrophilic solutes and micro organic pollutants, where the former was used to evaluate the molecular sieving effect of this membrane and the latter was employed for the investigation of solute-membrane interaction as hydrophobic materials. This membrane effectively rejected the hydrophilic solutes and the permeation of them was mainly controlled by the molecular sieving effects such as molecular weight and molecular width. In the case of all micro organic pollutants, the rejections were varied from 42.2% for Simazine to 91.6% for Malathion, and the parameters related to the steric hindrance could significantly play an important role in the rejection. In the batch type adsorption experiments, all micro organic pollutants were entrapped mildly on the membrane in spite of lower degree compared with that of aromatic compounds, and they were correlated with log K.

• 대한환경공학회지
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• 제31권9호
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• pp.793-802
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• 2009

매립가스의 자원화를 저해하는 전처리 대상물질 중 하나인 유기규소화합물(실록산)에 대한 흡착제의 제거특성을 확인하기 위하여 실제 매립가스를 대상으로 야자계 활성탄, 석탄계 활성탄, 실리카겔, 탈황제, 슬러지탄화물, molecular sieve 13X의 여섯 가지 상용 흡착제 등을 사용한 흡착실험을 수행하였다. 흡착제별 실록산 제거특성을 확인한 결과, 야자계 활성탄은 흡착된 L2성분의 급격한 유출이 확인되었으나 전체적인 실록산 제거효율과 흡착특성을 고려할 때 가장 우수한 흡착제로 나타났다. 그러나 실록산의 제거효과가 있는 것으로 알려져 있는 실리카겔의 경우에는 매립가스 중 D4와 D5 성분을 효과적으로 제거하였으나 L2성분은 흡착되지 않는 것으로 나타나 일부 실록산 성분의 제거효과만이 확인되었다. 한편, 야자계 활성탄을 직렬배열하였을 때, 처리된 매립가스의 실록산 함유정도와 농도변동의 주요인자인 L2성분을 비롯한 실록산 성분의 안정적인 제거가 가능한 것으로 나타났다. 또한, 실제 매립가스를 구성하고 있는 매우 다양한 성분들의 특성과 상호작용으로 흡착제의 실록산 제거특성에 영향을 미치는 것으로 나타나 효율적인 매립가스 자원화를 위해서는 흡착제와 대상물질 사이의 흡착특성과 함께 매립가스에 포함된 처리대상물질의 배출특성에 따른 전처리가 이루어져야 함을 확인할 수 있었다.