• Bulletin of the Korean Chemical Society
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• 제22권4호
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• pp.405-408
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• 2001

New lipophilic triesters of calix[4]arene and calix[4]quinone are investigated as sodium ion-selective ionophores in poly(vinyl chloride) membrane electrodes. For an ion selective electrode based on calix[4]arene triester I, the linear response is 1 ${\times}$10-3.5 to 1 ${\times}$ 10-1 M of Na+ concentrations. The selectivity coefficients for sodium ion over alkali metal and ammonium ions are determined. The detection limit (logaNa+ = -4.50) and the selectivity coefficient (logKNa+,K+pot = -1.86) are obtained for polymeric membrane electrode containing calix[4]arene triester I.

• Bulletin of the Korean Chemical Society
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• 제22권12호
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• pp.1345-1349
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• 2001

New quadruply-bridged calix[6]arenes (I-V) have been studied as cesium selective ionophores in poly(vinyl chloride) (PVC) membrane electrodes. PVC membranes were prepared with dioctyl sebacate (DOS) or 2-nitrophenyl octyl ether (o-NPOE) as the sol vent mediator and potassium tetrakis(p-chlorophenyl)borate as the lipophilic salt additive. These ionophores produced electrodes with near-Nernstian slope. The selectivity coefficients for cesium ion with respect to alkali, alkaline earth and ammonium ions have been determined. The lowest detection limit (logaCs+ = -6.3) and the higher selectivity coefficient (logkpotCs+,Rb+ = -2.1 by SSM, -2.3 by FIM for calix[6]arene I) for Cs+ have been obtained for membranes containing quadruply-bridged calix[6]arenes (I, Ⅱ, Ⅲ), which have no para t-butyl substituents on the bridging benzene ring.

• 대한약학회:학술대회논문집
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• 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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• pp.401.1-401.1
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• 2002

Potentiometric sensors are important and viable devices for use in pharmaceutical analysis. liquid polymeric membrane electrodes for many basic drugs and a few acidic drug were reported. The acidic drug-metal(Ⅱ)-triethylene tetramine ion pair complexes were prepared and used in poly(vinyl chloride) membrane electrodes to analyze anionic drugs such as mefenamic acid and ibuprofen. Metal ion used were Fe2＋. Co2＋. Ni2＋ and Cu2＋. Plasticizer used was o-nitrophenyl octyl ether.. (omitted)

• 공업화학
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• 제21권4호
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• pp.475-478
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• 2010

불소화 반응을 통하여 PDMS을 질소 분위기 하에서 $50{\sim}2000\;{\mu}mol/mol$ 농도의 불소 가스($F_2$)를 사용하여 직접적인 방법으로 복합막 표면개질을 하였고 이를 OM (Optical Microscope), AFM (Atomic Force Microscope), SEM (Scanning electron microscope), FT-IR (Fourier transform infrared spectroscopy)을 측정하여 막 표면을 연구하였고 GC (Gas chromatography)로 혼합 노블가스의 기체 거동을 조사하였다. 다양한 노블 혼합 가스를 사용하여 표면 개질된 PDMS 멤브레인의 선택도가 50% 향상 되었다.

• 소성∙가공
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• 제14권5호
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• pp.473-476
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• 2005

The demand of on-chip total analyzing system with MEMS (micro electro mechanical system) bio/chemical sensor is rapidly increasing. In on-chip total analyzing system, to detect the bio/chemical products with submicron feature size, a filtration system with nano-filter is required. One of the conventional methods to fabricate nano-filter is to use direct patterning or RIE (reactive ion etching). However, those procedures are very costly and are not suitable fur mass production. In this study, we suggested new fabrication method for a nano-filter based on replication process, which is simple and low cost process. After the Si master was fabricated by laser interference lithography and reactive ion etching process, the polymeric mold was replicated by UV-imprint process. Metallic nano-filter was fabricated after removing the polymeric part of metal deposited polymeric mold. Finally, our fabrication method was applied to metallic nano-filter with $1{\mu}m$ pitch size and $0.4{\mu}m$ hole size for bacteria sensor application.

• Membrane and Water Treatment
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• 제9권3호
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• pp.147-153
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• 2018

This study investigates the role of microbial extracellular polymeric substances (EPSs) as bioflocculants to harvest microalgae (water-microalgae separation). The EPS extracted from waste activated sludge (WAS) by heat extraction were fractionated into soluble EPS (S-EPS), loosely-bound EPS (LB-EPS) and tightly-bound EPS (TB-EPS) forms. All the EPSs facilitated the flocculation of microalgal cells from stable growth medium. Of those EPSs, the TB-EPS showed the highest flocculating activity (FA) resulting in the substantial decrease in the amount of EPS added in terms of total organic carbon (TOC) during flocculation. The FA of microalgae was improved with the increase in TB-EPS dose, however, excessive dose of TB-EPS adversely affected it due to destabilization. Both LB- and TB-EPS could be utilized for flocculating microalgae as a sustainable option to the existing chemical-based flocculants. In addition to the conventional assessments, the effectiveness of the two bioflocculants for floc forming was also confirmed using a novel assessment of lens-free shadow imaging technique (LSIT), which was firstly applied for the rapid and quantitative assessment of microalgal flocculation.

• Molecules and Cells
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• 제26권4호
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• pp.356-361
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• 2008

In this work, we have studied the structural and functional linkage between lamin A/C, nuclear actin, and organization of chromosome territories (CTs) in mammary carcinoma MCF-7 cells. Selective down-regulation of lamin A/C expression led to disruption of the lamin A/C perinuclear layer and disorganization of lamin-bound emerin complexes at the inner nuclear membrane. The silencing of lamin A/C expression resulted in a decrease in the volume and surface area of chromosome territories, especially in chromosomes with high heterochromatin content. Inhibition of actin polymerization led to relaxation of the structure of chromosome territories, and an increase in the volumes and surface areas of the chromosome territories of human chromosomes 1, 2 and 13. The results show an important role of polymeric actin in the organization of the nuclei and the chromosome territories.

• 전기화학회지
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• 제10권4호
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• pp.295-300
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• 2007

A new characterization method using a porous plug model was proposed to determine the degree of sulfonation (DS) of ionomer binder with respect to the membrane used in membrane-electrode assemblies (MEAs) and to analyze the fraction of proton pathways through ionomer-catalyst combined electrodes in MEAs for polymer electrolyte fuel cells (PEFCs). Sulfonated poly(ether ether ketone) was prepared to use a polymeric electrolyte and laboratory-made SPEEK solution (5wt.%, DMAc based) was added to catalyst slurry to form catalyst layers. In case of the SPEEK-based MEAs in this study, DS of ionomer binder for catalyst layers should be the same or higher than that of the SPEEK membrane used in the MEAs. The porous plug model suggested that most of protons were via the ionomer binder (${\sim}92.5%$) bridging the catalyst surface to the polymeric electrolyte, compared with the pathways through the alternative between the interstitial water on the surface of ionomer binder or catalyst and the ionomer binder (${\sim}7.3%$) and through only the interstitial water on the surface of ionomer or catalyst (${\sim}0.2%$) in the electrode of the MEA comprising of the sulfonated poly(ether ether ketone) membrane and the 5wt.% SPEEK ionomer binder. As a result, it was believed that the majority of proton at both electrodeds moves through ionomer binder until reaching to electrolyte membrane. The porous plug model of the electrodes of MEAs reemphasized the importance of well-optimized structure of ionomer binder and catalyst for fuel cells.

• 멤브레인
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• 제29권4호
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• pp.223-230
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• 2019

본 논문에서는 이산화탄소 친화적인 PBEM-POEM (PBE) 공중합체를 기반으로 고분자 블렌드 분리막을 제조하는 방법을 제시한다. PBE 공중합체는 자유 라디칼 중합 반응을 통해 손쉽게 합성이 가능하며, 이를 상용 고분자인 PEG와 다양한 비율로 혼합하여 이산화탄소/질소 분리막을 제조하였다. 이산화탄소/질소 분리 성능을 테스트한 결과, PEG의 함량이 높을수록 이산화탄소 투과도는 감소하는 반면 이산화탄소/질소 선택도는 크게 증가하는 상충(trade-off) 관계가 나타났다. 그러나 PBE/PEG (9 : 1)과 PBE/PEG (7 : 3)을 비교하면 이산화탄소 투과도는 단지 8.3% 감소한 반면에 질소 투과도는 69.1%나 감소하였다. 따라서 이산화탄소/질소 선택도가 33.8에서 100.3으로 크게 증가하였다. 이것은 PBE 공중합체의 80%를 차지하는 POEM 사슬이 PEG와 상호작용하여 더욱 조밀한 구조가 되었기 때문이며, 이를 FT-IR, XRD, SEM 분석으로 확인하였다. PBE/PEG (7 : 3) 블렌드 막이 가장 최적의 기체 분리 성능을 가졌고, 이산화탄소투과도는 170.5 GPU, 이산화탄소/질소 선택도는 100.3이었다.

• 센서학회지
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• 제5권4호
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• pp.35-40
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• 1996

수소이온운반체로 HDBA(hexyldibenzylamine)나 HDPA(hexyldiphenylamine)을 이용하여 고분자막 pH 센서를 제작하였고, 온도 및 막의 두께 변화에 대한 전기화학적 특성을 연구하였다. HDPA를 이용한 센서는 수소이온에 대하여 선택적으로 감응하지 않았으며, HDBA를 이용한 센서는 pH 2 - pH 10 범위에서 수소이온에 대하여 선형적이고, 응답시간도 30 - 50초로 매우 빠르며, Nernstian 기울기는 53.6mV/pH을 나타내었다. pH 센서는 유리전극과 비교하여 알칼리금속과 알칼리토 금속이온에 대하여 방해를 적게 받았고, 재현성 및 안정성에 대한 편차는 2 - 4mV(${\pm}0.1mV$)로 우수하게 나타내었다.