• 상하수도학회지
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• 제28권1호
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• pp.83-89
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• 2014

The aim of this study is to investigate the sorption/ion exchange of radioactive nuclides such as $Cs^+$ and $Sr^{2+}$ by synthetic Na-micas. In order to prepare Na-micas, two natural micas (phlogopite and biotite) were used as precursor materials. XRD, SEM, and EDS analyses were used to examine material characterization of synthetic Na-micas. Analyses of materials revealed that Na-micas were successfully obtained from natrual micas by K removal treatment. On the other hand, single solute (Cs or Sr) and bi-solute (Cs/Sr) sorption experiments were carried out to determine sorption capacity of Na-micas for Cs and Sr under different pH and ionic strength conditions. Uptake of Cs and Sr by micas in bi-solute system was lower than in single-solute system. Additionally, Langmuir and Langmuir competitive models were applied to describe sorption isotherm of Na-micas. bi-solute system was well described by Langmuir competitive models. For the results obtained in this study, Na-micas could be promising sorbents to treat multi-radioactive species from water and groundwater.

• Membrane and Water Treatment
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• 제6권2호
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• pp.127-139
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• 2015

Rejection of ionic solutes by reverse osmosis (RO) and nanofiltration (NF) membranes is controlled mainly by electrochemical interaction as well as pore size, but it is very difficult to directly evaluate such electrochemical interaction. In this work, we used an inverse HPLC method to investigate the interaction between ionic solutes and poly (m- phenylenediaminetrimesoyl) (PPT), a polymer similar to the skin layer of polyamide RO and NF membranes. Silica gel particles coated with PPT were used as the stationary phase, and aqueous solutions of the ionic solutes were used as the mobile phase. Chromatographs obtained for the ionic solutes showed features typical of exclusion chromatographs: the ionic solutes were eluted faster than water (mobile phase), and the exclusion intensity of the ionic solute decreased with increasing solute concentration, asymptotically approaching a minimum value. The charge density of PPT was estimated to be ca. 0.007 mol/L. On the basis of minimum exclusion intensity, the exclusion distances between a salt and neutralized PPT was examined, and the following average values were obtained: 0.49 nm for 1:1 salts, 0.57 nm for 2:1 salts, 0.60 nm for 1:2 salts, and 0.66 nm for 2:2 salts. However, $NaAsO_2$ and $H_3BO_3$, which are dissolved at neutral pH in their undissociated forms, were not excluded.

• 한국막학회:학술대회논문집
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• 한국막학회 2000년도 추계 총회 및 국제학술발표회
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• pp.71-74
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• 2000

• 멤브레인
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• 제13권1호
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• pp.29-36
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• 2003

A characterization of the permeation and separation using single salt solution was carried out with charged composite membranes. Various charged composite membranes were fabricated by blending an ionic polymer with a nonionic polymer in different ratios. In this study, sodium alginate, chitosan and poly(vinyl alcohol) were employed as anionic, cationic and nonionic polymers, respectively. The permeation and separation behaviors of the aqueous salt solutions have been investigated through the charged composite membranes with various charge densities. As the content of the ionic polymer increased in the membrane, the hydrophilicity of the membrane increased, and pure water flux and the solution flux increased correspondingly, indicating that the permeation performance through the membrane is determined mainly by its hydrophilicity. Electrostatic interaction between the charged membrane and ionic solute molecules, that is, Donnan exclusion, was observed to be attributed to salt rejection to a greater extent, and molecular sieve mechanism was effective for the separation of salts under a similar electrostatic circumstance of solutes.

• Bulletin of the Korean Chemical Society
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• 제24권1호
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• pp.55-59
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• 2003

This work is focused on analyzing ion-pair interactions and showing the effect of solvent induced inter-atomic attractions in various dielectric environments. To estimate the stability of ion-pairs, SCI-PCM ab initio MO calculations were carried out. We show that the solvent-induced attraction or ‘cavitation' energy of the ion-pair interactions in solution that arises mainly from the stabilization of the water molecules by the generation of an electrostatic field. In fact, even the strong electrostatic interaction characteristic of ion-pair interactions in the gas phase cannot overcome the destabilization or reorganization of the water molecules around solute cavities that arise from cancellation of the electrostatic field. The solvent environment, possibly supplemented by some specific solvent molecules, may help place the solute molecule in a cavity whose surroundings are characterized by an infinite polarizable dielectric medium. This behavior suggests that hydrophobic residues at a protein surface could easily contact the side chains of other nearby residues through the solvent environment, instead of by direct intra-molecular interactions.

• 멤브레인
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• 제11권1호
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• pp.22-28
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• 2001

이온성 고분자에 비이온성 고분자를 섞어 이온 함량을 조절함으로써 다양한 전하량을 갖는 이온성 막을 제조하였다. 비이온성 고분자로는 폴리비닐알콜, 음이온성 고분자로는 알긴산 나트륨, 양이온성 고분자로는 키토산을 사용하였으며, 이들 이온성 고분자막을 사용하여 여러 전해질 수용액에 대한 투과 및 분리특성을 관찰하였다. 막 내부에 이온성 고분자 함량이 많을수록 친수성 특성을 보였으며, 순수투과 및 용액투과 속도가 증가함을 관찰할 수 있었고, 또한 투과속도는 막의 팽윤 거동에 의해 결정됨을 확인할 수 있었다. 용질 배제율의 경우는 막과 투과용질간의 정전기적 인력, 즉 Donnan exclusion에 의해 결정이 되며, 정전기적 인력이 비슷한 경우는 분자체 효과에 의해 분리됨이 관찰되었다.

• 자원환경지질
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• 제45권5호
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• pp.525-533
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• 2012

겨울철동안 쌓여 봄에 놓은 눈 녹은 물(snowmelt), 즉 융설의 유출은 북반구 및 산간지역에서 매우 중요한 것으로 여겨지고 있다. 이러한 지역에서 융설로 인한 유동 및 이온의 이동에 대한 이해는 매우 중요하며 전세계적으로 꾸준하게 연구되고 있다. Lee et al. (2008a)와 Lee et al. (2008b)연구에서는 대기로부터 수송된 이온 및 오염원이 융설에 의해 눈속을 이동하는 것을 모사하기 위한 Mobile-Immobile water Model (MIM)을 개발하였다. 이 연구에 사용된 모델을 검증하기 위해서 물질수지계산(mass balance calculation) 및 해석해(analytical solution)를 이용한 모델결과와의 비교를 수행하였다. 일정시간동안 눈 속에서의 물질의 질량변화는 눈 표면에서 들어온 물질과 눈 기저부에서 빠져나간 물질의 질량 차이와 같아야한다는 사실을 이용하여 물질수지를 계산하였다. 파면(wave front)의 이동속도 및 기존문헌에서 알려진 해석 해를 이용하여 모델결과와의 비교도 시도하였다. 모델의 물질수지계산결과 질량 차이가 거의 발생하지 않았으며 모델결과와 해석해와의 비교 역시 두 결과가 거의 일치하였다.

• Membrane and Water Treatment
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• 제13권2호
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• pp.63-72
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• 2022

Choline chloride-glycerol (1:2 mol), a natural deep eutectic solvent (NADES) is examined as a draw solution in forward osmosis (FO) for dewatering application. The NADES is easy to prepare, low in toxicity and environmentally benign. A polyamide thin film composite membrane was used. Characterization of the membrane confirmed porous membrane structure with good hydrophilicity and a low structural parameter (722 ㎛) suitable for FO application. A dilute solution of 20% (v/v) NADES was enough to generate moderate water flux (14.98 L m^-2h^-1) with relatively low reverse solute flux (0.125 g m^-2h^-1) with deionized water feed. Application in dewatering industrial wastewater feed showed reasonably good water flux (11.9 L m^-2h^-1) which could be maintained by controlling the external concentration polarization and fouling/scaling mitigation via simple periodic deionized water wash. In another application, clarified sugarcane juice could be successfully concentrated. Recovery of the draw solute was accomplished easily by chilling utilizing thermo responsive phase transition property of NADES. This study established that low concentration NADES can be a viable alternative as a draw solute for dewatering of wastewater and other heat sensitive applications along with a simple recovery process.

• 약학회지
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• 제30권6호
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• pp.306-310
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• 1986

The release of heparin from monolithic devices composed of different ratios of polyethylene oxide(PEO MW 20,000) and polydimethylsiloxane was investigated. Water soluble PEO plended into the polydimethylsiloxane proved a controlled release of heparin. The release rate of heparin could be controlled by varying the content of PEO and loading dose of heparin. The release rate of heparin from the devices increased as the content of PEO and heparin in the devices increased. The release rate of heparin from devices were related to nature of solute(ionic strength) and temperature. The release mechanism may be associated with the creation of pore or domine through the devices the water-uptake and the change in the physical structure of the polydimethysiloxane network.

• Korean Membrane Journal
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• 제5권1호
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• pp.54-60
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• 2003

The rejection properties and flux rates of silica nanoparticles in ultrafiltration membranes has been investigated. Cross-flow permeation experiments were conducted using polycarbonate track-etch flat membranes with pore sizes of 30 and 50 nm, and a silica nanoparticle solute with particle sizes of 5 and 18 nm with narrow size distributions. The fluxes and rejection factors were investigated at various particle concentrations, cross-flow velocities, pH, and ionic strengths of solution. Even though the size of the silica nanoparticles was much smaller than that of the membrane pores, the observed rejection rates were very high compared with those for a similar-sized polymer (dextran). The observed rejection rate decreased with increasing ionic strength, which implies that the transport mechanism of the silica nanoparticles is significantly influenced by electrostatic repulsion between particles and membranes.