• 멤브레인
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• 제12권4호
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• pp.207-215
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• 2002

한정된 미세공간에서의 제한확산(hindered diffusion)은 멤브레인 기공(pore)에서 입자들의 운동에 의해 결정되는 여과 메카니즘을 매우 미세한 수준에서 이해하는데 중요한 현상이다. 구형(spherical) 콜로이드 입자에 비해 보다 복잡한 형태(conformation)인 고분자사슬 구조를 갖는 다가전해질(polyelectrolyte)의 제한확산 거동에는 다양한 인자들이 관련되어 있기 때문에, 이론 접근은 물론 실험적 접근도 한층 어려운 것이 사실이다. 본 연구에서는, 슬릿형 미세기공에 한정되어 있는 단일한 다가전해질(single polyelectrolyte)에 coarse-grained bead spring model과 먼거리(long-range) 정전상호작용(electrostatic interaction)인 Debye-Huckel potential을 적용하여 분자시뮬레이션 기법인 브라운 동력학 모사를 수행하였다. 기공과 다가전해질 사슬(Polyelectrolyte chain)의 주어진 크기에서, 용액의 전해질 이온농도가 감소함에 따른 사슬의 신장(extension)효과는 제한확산계수를 감소시켰고, 기공 벽면의 하전성은 제한확산계수를 더욱 감소시켰다. 이는, 다가전해질 사슬(polyelectrolyte chain)의 입체적 장애(steric hindrance)와 함께 정전반발력이 미세기공에서의 확산이동을 억제함을 의미한다.

• 멤브레인
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• 제4권2호
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• pp.85-95
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• 1994

이 논문은 막을 통한 전기적 여과시 동적이동현상을 연구하는데 있다. 액상에서의 전기적 대류는 막내에서의 전하고분자 물질의 속도를 증진시키는데, 이 문제의 해법은 액상과 교상의 직접적인 접촉을 통해 연구되었다. 연산자이론이 이 문제를 풀기 위해 적용되었고, 막에서의 물리적 변수들을 분석하는데 이용되었다. 이논문의 이론적 고찰은 분리조작 설계하는데 이용된다.

• Korean Membrane Journal
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• 제10권1호
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• pp.39-45
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• 2008

Polyelectrolyte complex based on two anionic polysaccharides, composed of sodium alginate and carrageenan, were prepared by interacting with divalent calcium ions in solution. The effects of annealing on the structural deformation of polyelectrolyte complex and on their characteristics at removing water from a methanol mixture from the point of molecular sieve were investigated and discussed. The result showed that the structural deformation of the annealed polyelectrolyte complex has an effect on the free volume between these polymer chains and the chelate segments such a shrinking of the overall morphology, which act as a molecular sieve in the separation of methanol and water mixtures.

• Macromolecular Research
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• 제16권4호
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• pp.308-313
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• 2008

A simple strategy was developed based on polyelectrolyte/silver nanocomposite to obtain humidity-sensitive membranes. The major component of a humid membrane is the polyTEAMPS/silver nanocomposite obtained by thermal heating the mixture of a polyelectrolyte and silver isopropylcarbamate complex. Humidity sensors prepared from polyTEAMPS/silver (w/w=100/0 and 100/6) nanocomposites had an average impedance of 292, 8.83 and $0.86\;k{\Omega}$, and 5,327, 140 and $0.93\;k{\Omega}$ at 30,60 and 95% relative humidity (RH), respectively. Hysteresis, temperature dependence and response time were also measured. Activation energies and complex impedance spectroscopy of the various components of the polyelectrolyte/silver nanocomposite films were examined for the humidity-sensing membrane.

• 한국막학회:학술대회논문집
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• 한국막학회 2004년도 Proceedings of the second conference of aseanian membrane society
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• pp.207-210
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• 2004

The pore-filled anion-exchange membranes were prepared in this study with an asymmetric poly(vinylidene fluoride)(PVDF) membrane as a nascent membrane and poly(vinylbenzyl chloride)(PVBCl) as a polyelectrolyte. The solution of PVBCI having the chloromethylate aryl ring of 80 percents and 1,4-diaminobicyclo [2,2,2]octane(DABCO) was made with the solvent of tetrahydrofuran(THF) and N,N-Dimethylformamide(DMF), which is in the rotio of 8:2. A new preparation method in this study, i.e. in-situ crosslinking, enabled us to produce the pore-filled membranes without change of size, and to control the properties of final membrane with various degree of cross-linking. From the result of surface morphologies of SEM and AFM the polyelectrolyte exists in the pores of nascent membrane as a certain configuration. From the investigation of the solvent affecting much to the permeability and rejection, it was found. that the membranes using DMF and THF showed better performances than the membranes produced by THF only. The water permeability of the final membrane at low pressure(100㎪) showed a typical ultrafiltation membrane's permeability (8-10kg/㎡hr) and good values of rejection(55∼60 percent).

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2003년도 총회 및 춘계학술발표회
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• pp.128-131
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• 2003

It is well known that the membrane separation process combined with surfactant micelle (micellar-enhanced ultrafiltration) or polyelectrolyte (polyelectrolyte-enhanced ultrafiltration) can remove heavy metals effectively. However, the environmental hazard of surfactant or polyelectrolyte remained in effluent is a serious disadvantage of these methods. In this study, humic substances (HS) were used as complexing agents for metal removal instead of synthetic chemicals. The HS are a sort of natural organic matters which are biodegradable and abundant in natural environment. And the functional groups such as carboxyl groups and phenols in HS can bind with the cationic radionuclides and form complexes. Therefore separation process using them will be more environmental-friendly. The effects of concentration of HS and pH on the removal of cobalt were investigated. The ultrafiltration process was applied to the separation of the cobalt - HS complexes from the aqueous stream. At the concentration of > 3 g/L of HS and pH of 6, over 95 % of cobalt was removed by regenerated cellulose membrane of molecular weight cut-off (MWCO) 3,000. As the concentration of HS increased, the removal of cobalt also was improved because of increase in biding sites (functional groups). The cobalt removal increased from 72.5 % to 97.5 % when pH increased from 4 to 8 at the concentration of 3 g/L HS because of increase in HS solubility and cobalt hydroxide precipitation. In the presence of NaCl, the removal efficiency of cobalt decreased.

• 한국막학회:학술대회논문집
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• 한국막학회 1996년도 춘계 총회 및 학술발표회
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• pp.60-61
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• 1996

Polyanion-polycation complexes had been known for a long time on an empirical basis fromthe mutual precipitation of proteins, before Kossel at the end of the previous century recognized the electrostatic nature of the interaction between oppositely charged polyions. The formation of polyelectmlyte complexes is essentially a result of the electrostatic nature of the interaction between oppositely charged polyions. This interaction in the macroscopic homogeneous system the phase transition by polysalt precipitation as well as the chemical and physical structure of polyelectrolyte complex membranes have been intensively investigated from the themodynamical and kinetical point of view.

• 공업화학
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• 제4권1호
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• pp.188-195
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• 1993

생체의료용 재료로서 응용 가능한 고분자 전해질복합체와 그라프트 공중합체를 수용성 고분자 유도체로부터 제조하였다. 고분자 전해질 복합체들은 카르복시메틸 셀룰로오즈(CMC)와 젤라틴으로부터 제조하였다. 그라프트 공중합체는 메틸셀룰로오즈(MC)에 아크릴산을 그라프트반응시켜 합성하였고, 이 그라프트 공중합체와 젤라틴의 고분자 전해질 복합체도 제조하였다. 그라프트 공중합체와 고분자 전해질 복합체들을 화학가교법과 열처리법으로 제조시 최적조건들을 조사하였다. 예비실험 결과 이들 재료들이 생체의료용 재료로서의 응용 가능성이 있는 것을 알았다.

• 멤브레인
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• 제23권4호
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• pp.304-311
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• 2013

발효공정으로부터 생산된 유기산의 회수를 위하여 나노여과 분리막 공정을 이용하는 경우 유기산을 제외한 발효액 내 존재하는 당, 단백질 등의 부산물을 배제하면서 유기산을 선택적으로 투과시킬 수 있는 나노여과막이 요구된다. 본 연구에서는 발효액으로부터 분자량이 상대적으로 작고 카르복실산기를 갖는 유기산의 효과적인 회수를 위하여 분리막 표면에 양전하를 도입하여 전기적 인력에 의해 젖산의 투과도를 향상시킬 수 있는 신규 나노여과 분리막을 제조하였다. 분리막 표면에 고분자 전해질 PEI (Polyethyleneimine)를 그라프팅시켜 제조된 분리막의 제타전위 측정 결과 표면 층이 양전하를 나타내는 것을 확인하였다. 실제 젖산 용액 배제율 확인 결과 고분자 전해질 그라프팅 층이 형성된 막에서 배제율이 크게 감소하는 것으로 보아 그라프팅 층에 의한 젖산 배제율 저감에 효과를 나타내었다.

• 분석과학
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• 제8권4호
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• pp.561-568
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• 1995

Two methods, precipitation and ultrafiltration, were applied in order to recover platinum group metals(PGM) by complexing them with water-soluble polyelectrolytes, e.g., polyethyleneimine [PEl], poly(2-vinylpyridine) [2-PVP], poly (4-vinylpyridine) [4-PVP], and poly (styrene sulfonic acid) [PSSA]. In the precipitation method, the PGM-polyelectrolyte complex that was formed by mixing first with polybase, e.g.,4-PVP at pH 1 was precipitated by further mixing with polyacid, e.g., PSSA. However, the recovery of PGM obtained by this method was not quantitative(less than 70%). The "sandwiching" binding between the metal anions and two polyelectrolytes was examined by X-ray photoelectron spectroscopy(XPS). The XPS studies indicated that the PGM atom was bound with the acdic and basic polyelectrolyte via its oxygen and nitrogen atom, respectively. The recovery of PGM using polyelectrolyte was further studied by ultrafiltration methods as follows : The PGM ions, eomplexed at pH 1 with polyelectrolyte, allowed the applicntion of membrane filtration by virtue of the great differences in molecular weights between PGM and other low molecular weight species. By applying this method, Pd and Pt (ca. $10^{-4}M$) were selectively separated almost quantitatively from coexisting metal ions, e.g., $Cu^{2+}$ and $Ni^{2+}$. The EPR spectra and viscosity measurements indicated that these polyelectrlytes were not bound to $Cu^{2+}$ and $Ni^{2+}$ ions at this pH, which provided the basis for selective separation of PGM(Pd, Pt and Rh) from these coexisting ions.