• 한국고분자학회:학술대회논문집
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• 한국고분자학회 2006년도 IUPAC International Symposium on Advanced Polymers for Emerging Technologies
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• pp.302-302
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• 2006

Nanoaggregates of triple hydrophilic block copolymers comprised of poly(ethylene oxide), poly(sodium 2-acrylamido)-2-methylpropanesulfonate), and poly(methacrylic acid) (PEO-PAMPS-PMAA) and the cationic surfactant, dodecyltrimethylammonium chloride (DTAC) have been fabricated. The formation of $^{\circ}^{\circ}$the nanoaggregates is based on electrostatic interaction of sulfonate and carboxylate groups of PAMPS and PMAA blocks with the cationic surfactant, which results in insolubilization of these blocks. The formation of micelle is observed by dynamic light scattering measurements. Binding of DTAC to the anionic blocks of PEO-PAMPS-PMAA is confirmed by electrophoresis measurements.

• Korean Membrane Journal
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• 제9권1호
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• pp.57-63
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• 2007

Amphiphilic graft copolymer from poly(vinylidene fluoride) (PVDF) was synthesized using atom transfer radical polymerization (ATRP) for composite nanofiltration membranes. Direct initiation of the secondary fluorinated site of PVDF facilitates grafting of tert-butyl methacrylate (tBMA). Amphiphilic PVDF-g-PMAA graft copolymer with a 51:49 wt ratio was obtained by hydrolyzing poly(tert-butyl methacrylate) (PtBMA) to poly(methacrylic acid) (PMAA). Wide angle X-ray scattering (WAXS) and differential scanning calorimetry (DSC) confirmed the decrease of crystallinity of PVDF upon graft copolymerization. Composite nanofiltration membranes were prepared from PVDF-g-PMAA as a top layer coated onto PVDF ultrafiltration (UF) support membrane. The morphology and hydrophilicity of membranes were characterized using scanning electron microscopy (SEM) and contact angle measurement. The rejections of composite membranes were 80.2% for $Na_2SO_4$ and 28.4% for NaCl, and the solution flux were 9.5 and $14.5\;L/m^2\;h$ at 1.0 MPa pressure.

• The Korean Journal of Ceramics
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• 제4권4호
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• pp.292-296
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• 1998

In wet powder processing of alumina, a number of organic molecules such as dispersant and binder are used to produce the flow behavior and properties requisite for shape forming. In this study, interparticle forces of alumina particles suspended in aqueous media were controlled by suspension pH, poly (methacrylic acid) (PMAA, used as dispersant) and poly (vinyl alcohol) (PVA, used as binder). The combined adsorption isotherms of the dispersant and binder additives on alumina were determined by total organic carbon analyzer, while the adsorption of dispersant was differentiated from binder in the mixed additive system by ultraviolet spectroscopy. The electrokinetic behavior of alumina suspensions were then correlated with the adsorption characteristics of dispersant and binder onto alumina particles. It was found that the isoelectric ($pH_{iep}$) of alumina shifted from pH 8.9${\pm}$0.1 to acidic pH as PMAA concentration increased, while PVA adsorption did not affect the $pH_{iep}$ but caused a decrease in the near surface potential.

• Bulletin of the Korean Chemical Society
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• 제14권5호
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• pp.574-578
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• 1993

Laser-induced photoacoustic spectroscopy (LIPAS), which utilizes the photothermal effect that results from nonradiative relaxation of excited state molecules, was used in the speciation analysis of the complexes of neodymium(III) and water soluble synthetic polyelectrolyte, poly methacrylic acid (PMAA), in 0.1 M $NaClO_4$ at pH of 6.0. The minimum detection limit of Nd(III) by LIPAS was $5.O{\times}10^{-6}$ M. Experiment was carried out at low concentration ratio of Nd(III) to PMAA to assure that 1 : 1 complexes predominate. The bound and free Nd(III) species were characterized by measuring nonradiative relaxation energy of the excited states $(^2GM{7/2}\;and\;^4G_{5/2})$ to the metastable state $(^4G_{3/2})$. Two species were quantified by deconvolution of the mixed spectrum using their respective reference spectra. The conditional stability constant measured by LIPAS was 5.52 L$mol^{-1}$.

• 한국세라믹학회지
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• 제36권3호
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• pp.266-273
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• 1999

본 연구에서는 겔캐스팅법의 제조공정 확립을 위하여 분산제의 분자구조가 질화규소 슬립의 점성특성 및 성형체의 상대밀도와 기계적 특성에 미치는 영향을 조사하였다. 슬립과 겔캐스팅 성형체의 제조방법은 기보고된 방법과 동일하게 하였다. 그 결과, 겔캐스팅 슬립의 점성은 분산제의 분자구조와 모노머와 분산제의 구성비율에 크게 의존하였다. PMAA 분산제를 사용한 슬립의 점성은 PAA 및 PAAm 분산제 보다 높은 점도를 나타내었다. 성형체의 상대밀도는 슬립의 농도에 크게 의존하였으며, 분산제양과 모노머의 양변화에는 그다지 변화가 없었다. 그리고, 겔캐스팅 성형체의 기계적 특성은 크게 모노머의 농도에 의존하였으며, 분산제양과 슬립의 농도에는 큰 변화가 없었다.

• 한국염색가공학회지
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• 제5권1호
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• pp.19-25
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• 1993

Plastic optical fibers(POFs) composed of poly(methylmethacrylate) (PMMA), polystyrene (PS), or polycarbonate(PC) as a core materials, and of fluorinated polymer or PMMA as a cladding were fabricated and their properties were investigated in this study. The attenuation loss of PMAA core POF was about 1,700 dB/Km at 660 nm, the loss of PS core POF was 1,800 dB/Km at 560 nm, and the loss of PC core POF was 2,200 dB/Km at 780 nm. These attenuation losses of POFs prepared ill this study were higher than those of commerically available POFs. Compared to PMMA and PS core POFs, PC core POF has excellent characteristics, including high thermal stability, high flexibility, and high impact strength.

• 센서학회지
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• 제6권1호
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• pp.35-42
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• 1997

전기적 제한 방출 시스템을 이용한 페록사이드 측정용 광바이오센서가 개발되었다. HPA를 포함한 PEOx와 PMAA의 고분자 복합체는 전류를 가하게 되면 붕괴되면서, HPA를 방출한다. 고분자 복합체의 붕괴 속도 및 방출되는 HPA의 양은 가해지는 전류의 세기에 비례했다. 페록사이드는 HPA와 페록시다아제효소에 의해 반응되어 형광 물질인 DBDA가 생성되었다. Xenon램프를 이용하여 DBDA를 여기시키고 발생되는 형광을 광섬유와 광다이오드어레이로 측정하였다. 측정된 DBDA의 형광의 변화는 페록사이드의 농도에 비례하였다. 페록시다아제 효소는 Ca-alginate를 이용하여 반응기내벽에 고정화시켰다. 개발된 광바이오센서는 페록사이드 0.025mM - 1.0mM 농도의 측정 범위를 가지며, 페록사이드의 단계 변화에 대한 반복성 있는 센서신호가 조사되었다. 효소 반응과 물질전달현상을 통하여 센서의 수학적 모델을 구성하였으며, 제안된 모델은 실험 결과와 잘 일치함을 알 수 있었다.

• Korean Chemical Engineering Research
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• 제47권4호
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• pp.453-458
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• 2009

최근 환경문제가 크게 대두됨에 따라 고분자 합성과 가공 공정에서도 유기용매를 사용하지 않는 새로운 친환경적 공정의 개발이 요구되고 있다. 초임계 이산화탄소는 고분자 합성에서 용매로 사용될 경우, 기존의 유기용매와 비교하여 불연성이고 독성이 없으며 생성물과의 분리가 용이하다는 장점을 가지고 있다. 본 연구에서는 초임계 이산화탄소를 이용하여 의약학 및 화장품 분야에서 지능형 약물전달체로 사용할 수 있는 pH 감응형 하이드로젤인 P(MAA-co-EGMA) 하이드로젤을 수 백 nm 수준의 입자 형태로 합성하는 방법을 개발하였다. 그리고 중합과정에서 사용하는 분산안정제인 PtBuMA-PEO와 중합개시제인 AIBN이 하이드로젤 입자의 합성에 미치는 영향을 살펴보았다. 입자의 합성에서 PtBuMA-PEO의 함량이 증가할수록 입자 크기는 감소하였으나 AIBN의 함량에 따른 입자 크기의 변화는 관찰할 수 없었다. 합성된 P(MAA-co-EGMA) 하이드로젤 입자의 pH에 따른 팽윤 실험결과, PMAA의 $pK_a$인 pH 5를 전후하여 급격한 하이드로젤의 평형 질량팽윤비의 변화를 관찰할 수 있었다. 즉, pH 5보다 낮은 pH에서는 낮은 팽윤비를, 반면에 pH 5보다 높은 pH에서는 매우 높은 팽윤비를 나타내었다. 그리고 Rh-B를 이용한 방출실험에서는 높은 pH에서는 다량의 Rh-B가 하이드로젤 입자로부터 방출되었으나 낮은 pH에서는 Rh-B가 거의 방출되지 않는 pH에 따른 선택적 방출 특성을 나타내었다.

• Macromolecular Research
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• 제13권6호
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• pp.483-490
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• 2005

A novel, polysaccharide-based, superabsorbent hydrogel was synthesized through crosslinking graft copolymerization of methacrylic acid (MAA) onto kappa-carrageenan ($_{k}C$), using ammonium persulfate (APS) as a free radical initiator in the presence of methylenebisacrylamide (MBA) as a crosslinker. A proposed mechanism for $_{k}C$­g-polymethacrylic acid ($_{k}C$-g-PMAA) formation was suggested and the hydrogel structure was confirmed using FTIR spectroscopy. The effect of grafting variables, including MBA, MAA, and APS concentration, was systematically optimized to achieve a hydrogel with the maximum possible swelling capacity. The swelling kinetics in distilled water and various salt solutions were preliminarily investigated. Absorbency in aqueous salt solutions of lithium chloride, sodium chloride, potassium chloride, calcium chloride, and aluminum chloride indicated that the swelling capacity decreased with increased ionic strength of the swelling medium. This behavior can be attributed to the charge screening effect for monovalent cations, as well as ionic crosslinking for multivalent cations. The swelling of super absorbing hydrogels was measured in solutions with pH ranging from 1 to 13. In addition, the pH reversibility and on-off switching behavior, at pH levels of 3.0 and 8.0, give the synthesized hydrogels great potential as an excellent candidate for the controlled delivery of bioactive agents.