• Macromolecular Research
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• 제12권1호
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• pp.94-99
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• 2004

We have performed Fourier transform infrared (FTIR) spectroscopy and differential scanning calorimetry (DSC) studies on blends of poly(vinyl phenol) (PVPh) with poly(n-alkylene 2,6-naphthalates) containing alkylene units of different lengths. The results indicate that each poly(ethylene 2,6-naphthalate) (PEN) and poly(trimethylene 2,6-naphthalate) (PTN) blend with PVPh is immiscible or partially miscible, but blends of poly(butylene 2,6-naphthalate) (PBN) with PVPh are miscible over the whole range of compositions in the amorphous state. FTIR spectroscopic analysis confirmed that significant degree of intermolecular hydrogen bonding occurs between the PBN ester carbonyl groups and the PVPh hydroxyl groups. The large difference in the degree of mixing in these blend systems is described in terms of the effect that chain mobility has on the accessibility of the ester carbonyl functional groups toward the hydroxyl groups of PVPh, which in turn impacts the miscibility of these blends.

• Bulletin of the Korean Chemical Society
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• 제19권4호
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• pp.444-449
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• 1998

The kinetics of the formation of triplex $poly(dA){\cdot}[poly(dT)]_2$ from poly(dA)·poly(dT) and poly(dT) is examined by various optical spectroscopic methods, including absorption, circular and linear dichroism (LD) spectroscopy. In the pseudo first order condition, where the poly(dT) concentration is kept lower than that of duplex, the association of the poly(dT) is enhanced by the presence of ethidium; the rate constant is proportional to the amount of ethidium in the mixture. When the concentration of the duplex and the single strand is the same, a spectral change is explained by double exponential curves, indicating that at least two steps are involved, the fast association and slow rearrangement steps. In contrast to the pseudo first order kinetics, the association step in an equimolar condition is not affected by the presence of ethidium. In the rearrangement step, the magnitude of LD decreases with an increase in ethidium concentration, suggesting that the bending of polynucleotide around the intercalation site occurs in the rearrangement step.

• Macromolecular Research
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• 제9권5호
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• pp.277-284
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• 2001

Poly(exo-3,6-epoxy-1,2,3,6-tetrahydrophthalic anhydride)s [poly(ETA)s] and poly($\alpha$-ethoxy-exo-3,6-epoxy-1,2,3,6-tetrahydrophthaloyl-5-fluorouracil)s [poly(EETFU)s ] with various average molecular weights were prepared by photopolymerizations. The number average molecular weights of the fractionated poly(ETA)s and poly(EETFU)s determined by GPC were in the range of 3,600∼21,000 and 3,600-33,400, respectively. The release rate of 5-FU from poly(EETFU) decreased with increasing average molecular weight. The in vitro cytotoxicity of poly(ETA) against a normal cell line was lower than that of 5-fluorouracil(5-FU), The in vivo antitumor activities of the synthesized samples at dosage of 0.8 mg/kg against mice bearing sarcoma 180 tumor cell line decreased in the following order: poly(EETFU) > poly(ETA) > EETFU > ETA > 5-FU. The antiangiogenic activities of the poly(ETA)s were better than those of 5-FU.

• 공업화학
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• 제19권3호
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• pp.316-321
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• 2008

Styrene과 4-vinylpyridine의 공중합체(poly(st-co-4vp)) 입자를 무유화제 유화중합에 의해 합성하고 이 입자 내부에 iron pentacarbonyl을 침투시킨 후 열분해 시켜 입자의 표면과 내부에 산화철 나노입자를 갖는 자성 poly(st-co-4vp) 입자를 제조하였다. 얻어진 자성 poly(st-co-4vp) 입자의 크기와 분포, 열적 특성 및 자성 특성에 대해서 조사하였다. 자성 poly(st-co-4vp) 입자는 크기가 약 250 nm 정도로 매우 균일하였으며 약 14%의 산화철을 가졌다. 산화철은 XRD 시험에 의해 대부분 $Fe_3O_4$임이 확인되었으며 superconducting susceptometer (SQUID) 시험에 의해 자성 poly(st-co-4vp) 입자가 초상자성을 가짐을 확인하였다.

• 한국정보전자통신기술학회논문지
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• 제16권6호
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• pp.509-518
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• 2023

본 논문에서는 아날로그 회로 트리밍과 Calibration 등에 필요한 4Kb Poly-Fuse OTP IP를 설계하였다. NMOS Select 트랜지스터와 Poly-Fuse 링크로 구성된 Poly-Fuse OTP 셀의 BL 저항을 줄이기 위해 BL은 Metal 2와 Metal 3를 stack하였다. 그리고 BL 라우팅 저항을 줄이기 위해 4Kb 셀은 64행 × 32열 Sub-block 셀 어레이 2개로 나뉘었으며, BL 구동회로는 Top과 Bottom으로 나누어진 2Kb Sub-block 셀 어레이의 가운데에 위치하고 있다. 한편 본 논문에서는 1 Select 트랜지스터에 1 Poly-Fuse 링크를 사용하는 OTP 셀에 맞게 코어회로를 제안하였다. 그리고 OTP IP 개발 초기 단계에서 프로그램되지 않은 Poly-Fuse의 저항이 5kΩ까지 나올수 있는 경우까지를 고려한 데이터 센싱 회로를 제안하였다. 또한 Read 모드에서 프로그램되지 않은 Poly-Fuse 링크를 통해 흐르는 전류를 138㎂ 이하로 제한하였다. DB HiTek 90nm CMOS 공정으로 설계된 Poly-Fuse OTP 셀 사이즈는 11.43㎛ × 2.88㎛ (=32.9184㎛2)이고, 4Kb Poly-Fuse OTP IP 사이즈는 432.442㎛ × 524.6㎛ (=0.227mm²)이다.

• 대한수학회보
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• 제36권1호
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• pp.47-61
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• 1999

In this paper we difine poly-Euler numbers which generalize ordinary Euler numbers. We construct a p-adic poly-Euler measure by the poly-Euler polynomials and derive an integral formula.

• Membrane and Water Treatment
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• 제11권2호
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• pp.97-109
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• 2020

Membrane fouling is the main drawback of membrane technology. Frequent membrane cleaning and membrane replacement are, therefore, required to reduce membrane fouling that causes permeate flux reduction, lower rejection, or higher operating pressure. Studies have proved that the alteration of membrane properties is the key controlling factor in lessening membrane fouling. Among stimuli-responsive membranes, thermo-responsive membrane is the most popular, with a drastic phase transition and swelling-shrinking behavior caused by the temperature change. In this study, the thermo-responsive ability of two commercial membranes, PolyCera® Titan membrane and PolyCera® Hydro membrane, at different temperatures was studied on the antifouling function of the membrane in palm oil mill effluent (POME) treatment. The evaluation of the membrane's thermo-responsive ability was done through three cycles of adsorption (fouling) and desorption (defouling) processes in a membrane filtration process. The experimental result depicted that PolyCera® Hydro membrane had a higher membrane permeability of 67.869 L/㎡.h.bar than PolyCera® Titan membrane at 46.011 L/㎡.h.bar. However, the high membrane permeability of PolyCera® Hydro membrane was compensated with low removal efficiency. PolyCera® Titan membrane with a smaller mean pore size had better rejection performance than PolyCera® Hydro membrane for all tested parameters. On the other hand, PolyCera® Titan membrane had a better hydrodynamic cleaning efficiency than PolyCera® Hydro membrane regardless of the hydrodynamic cleaning temperature. The best hydrodynamic cleaning performed by PolyCera® Titan membrane was at 35℃ with the flux recovery ratio (FRR) of 99.17 ± 1.43%. The excellent thermo-responsive properties of the PolyCera® Titan membrane could eventually reduce the frequency of membrane replacement and lessen the use of chemicals for membrane cleaning. This outstanding exploration helps to provide a solution to the chemical industry and membrane technology bottleneck, which is the membrane fouling, thus reducing the operating cost incurred by the membrane fouling.

• 한국진공학회지
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• 제9권4호
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• pp.346-352
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• 2000

15%와 42%의 Ge함량을 갖는 poly $Si_{1-x}Ge_x$ 박막을 $700^{\circ}C$의 습식 산화 분위기에서 산화 공정을 진행하고, 박막의 산화 거동을 RBS, XPS, cross-sectional TEM으로 분석하였다. Poly $Si_{0.8}Ge_{0.15}$박막의 경우, $GeO_2$에 비해 열적으로 안정한 $SiO_2$가 우선 생성되고, 반응에 참여하지 못한 Ge은 산화막과 poly $Si_{1-x}Ge_{x}$박막의 계면에 축적되어 산화막 하부의 Ge농도가 증가함을 확인하였다. Poly $Si_{0.8}Ge_{0.42}$ 박막의 경우, 산화막내에 많은 양의 Ge이 $GeO_2$와 Ge 형태로 존재하였고, 이러한 $GeO_2$의 형성으로 인해 산화속도의 증가를 확인하였다. 이러한 분석 결과를 바탕으로 Ge 함량 증가에 따른 poly $Si_{1-x}Ge_x$ 박막의 산화 모델을 제시하였다.

• Macromolecular Research
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• 제8권1호
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• pp.26-33
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• 2000

A series of pH/temperature sensitive polymers were synthesized by copolymerizing N-isopro-pyl acrylamide(NIPAAm) and acrylic acid(AAc) . The influence of polyelectrolyte between poly(allyl amine) (PAA) and poly(L-lysine)(PLL) on the lower critical solution temperature(LCST) of pH/temperature sensitive polymer was compared in the range of pH 2∼12. The LCST of PNIPAAm/water in aqueous poly(NIPAAm-co-AAc) solution was determined by cloud point measurements. A polyelectrolyte complex was prepared by mixing poly(NIPAAm-co-AAc) with poly(allyl amine) (PAA) or poly(L-lysine) (PLL) solutions as anionic and cationic polyelectrolytes, respectively. The effect of polyelectrolyte complex formation on the conformation of PLL was studied as a function of temperature by means of circular dichroism(CD). The cloud points of PNIPAAm in the aqueous copolymers solutions were stongly affected by pH, the presence of polyelectrolyte solute, AAc content, and charge density. The polyelectrolyte complex was formed at neutral condition. The influence of more hydrophobic PLL as a polyelectrolyte on the cloud point of PNIPAAm in the aqueous copolymer solution was stronger than that of poly(allyl amine)(PAA). Although polymer-polymer complex was formed between poly(NIPAAm-co-AAc) and PLL, the conformational change of PLL did not occur due to steric hinderance of bulky N-isopropyl groups of PNIPAAm.

• 폴리머
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• 제24권4호
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• pp.477-487
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• 2000

Poly(L-lactic acid) (PLLA)/poly($\beta$-hydroxynonanoate) (PHN) 블렌드의 흔화도와 결정화거동을 연구하기 위해 여러 중량 흔합비의 시료를 제조하였다. DSC, XRD 및 편광현미경을 이용하여 PLLA/PHN 블렌드의 열적 성질 및 특성을 연구하였다. PLLA와 PHN은 무정형 영역에서 부분적인 상용성을 가졌으며 PLLA의 결정화도는 PHN이 첨가됨으로 인하여 증가되었다. 그리고 PHN이 첨가됨으로써 PLLA의 T$_{g}$, T$_{c}$, T$_{m}$ 의 이동이 있었다. 편광현미경 분석을 통하여 PLLA 구정의 수는 PHN이 증가할수록 증가하는 것을 알 수 있었다. 이로부터 PHN은 PLLA에 대하여 기핵제의 역할이 있음이 관찰되었다.