• Advances in environmental research
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• 제3권2호
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• pp.107-116
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• 2014

This study aimed to synthesize dispersed and reactive nanoscale zero-valent iron (nZVI) with poly(1-vinylpyrrolidone-co-vinyl acetate) (PVP/VA), nontoxic and biodegradable stabilizer. The nZVI used for the experiments was prepared by reduction of ferric solution in the presence of PVP/VA with specific weight ratios to iron contents. Colloidal stability was investigated based on the rate of sedimentation, hydrodynamic radius and zeta potential measurement. The characteristic time, which demonstrated dispersivity of particles resisting aggregation, increased from 21.2 min (bare nZVI) to 97.8 min with increasing amount of PVP/VA (the ratios of 2). For the most stable nZVI coated by PVP/VA, its reactivity was examined by nitrate reduction in a closed batch system. The pseudo-first-order kinetic rate constants for the nitrate reduction by the nanoparticles with PVP/VA ratios of 0 and 2 were 0.1633 and $0.1395min^{-1}$ respectively. A nitrogen mass balance, established by quantitative analysis of aqueous nitrogen species, showed that the addition of PVP/VA to nZVI can change the reduction capacity of the nanoparticles.

• 멤브레인
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• 제26권1호
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• pp.32-37
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• 2016

본 연구에서는 Poly(vinyl alcohol) $(PVA)/AgCF_3SO_3/Al(NO_3)_3$ 전해질 분리막을 제조하여 기존의 poly(vinylpyrrolidone) $(PVP)/AgCF_3SO_3/Al(NO_3)_3$ 분리막보다 더 향상된 성능을 보이는 고투과성 올레핀 촉진수송 분리막을 얻고자 하였다. $PVA/AgCF_3SO_3/Al(NO_3)_3$ 막의 특성은 SEM, FT-IR, FT-Raman에 의해서 조사되었다. 다양한 $Al(NO_3)_3$ 농도 중 1:1:0.01 $PVA/AgCF_3SO_3/Al(NO_3)_3$에서 가장 좋은 분리성능을 보였다. 결과적으로 선택도는 12, 혼합 기체 투과도는 3.5 Barrer를 나타내었으며, 선택도와 투과도는 115시간 동안 유지되었다.

• 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.412.2-413
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• 2002

Purpose. To prepare polymer based physical mixtures or solid dispersions containing solubilizing compositions using a spray-dryer. Methods. Lovastatin.simvastatin.aceclofenac and cisapride were selected as poorly water-soluble drugs. Dextrin. poly(vinylalcohol). poly(vinylpyrrolidone)and polyethylene glycol were chosen as solubilizing carriers for solid dispersions. The solid dispersions containing solubilizing compositions without drug were prepared without using organic solvents or tedious changes of formulation compositions. (omitted)

• 폴리머
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• 제29권3호
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• pp.266-270
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• 2005

Fe(CO)$_5$(철-펜타카보닐)의 열분해법을 이용하여 산화철 나노 입자를 제조하였다. 표면 조절 시약으로서 생체적 합성 고분자인 폴리(비닐피롤리돈)(PVP)을 사용하여 산화철 나노 입자의 크기를 제어하였다. 산화철 나노 입자의 형성 여부는 XRD를 통해 분석하였으며, PVP 코팅된 산화철 나노 입자의 크기는 TEM, ELS를 통하여 분석하였다. PVP 코팅 된 산화철 나노 입자의 입자 크기는 PVP/Fe(CO)$_5$의 몰비와 용매, PVP 분자량에 의해 조절되었다. PVP 함량이 증가함에 따라 입자 크기가 증가하였으며 디메틸포름아마이드를 용매로 하였을 때 $50\~100$ nm의 산화철 나노 클러스터가 형성되었고, Carbitol을 용매로 하였을 때 균일하게 분산된 10 nm 이하의 작은 PVP 코팅된 산화철 나노 입자가 형성되었다. 본 연구에서 제조된 PVP코팅된 산화철 나노 입자는 물에 잘 분산될 뿐 아니라 생체적합적인 PVP로 코팅이 되었기 때문에 in vivo에 응용할 수 있으며, 입자의 크기가 $50\~100$nm및 10 nm로 조절됨으로써 MRI 조영제로서 가능성을 가지고 있음을 확인하였다.

• Bulletin of the Korean Chemical Society
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• 제31권7호
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• pp.1869-1874
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• 2010

By reducing PVP with $H_2NOH$.HCl and NaOH 2:2:1 mass ratios in aqueous ethanol, poly-N-vinyl pyrrolidone oxime [PVPO] was prepared with 92% yield. Applying the sol-gel concept, orthosilicic acid [OSA] was made by hydrolyzing TEOS with ethanol in 1:0.5 molar ratios using 1 N KOH aqueous solution as a catalyst. The OSA + PVPO + $_L$-Valine ($\alpha$-amino acid) were mixed with pure ethanolic medium in 1:2:2 mass ratios and refluxed at $78^{\circ}C$ and 6 pH for 6.5 h. A white residue of poly-N-vinyl pyrrolidone oximo-L-valyl-siliconate [POVS] appeared after 5 h. The heating of reaction mixture was stopped and the contents were brought to NTP. The residue formation of POVS was intensified with lowering a temperature and completely solidified within 5 h, was filtered using a vacuum pump with Whatmann filter paper no. 42. The residue of POVS was washed several times with 20% aqueous cold ethanolic solution and dried in vacuum chamber at $25^{\circ}C$ for 24 h. The MP was noted above $350^{\circ}C$. Structural and internal morphology were analyzed with IR and $^1H$-NMR, and SEM respectively. A drug loading and transporting ability of the POVS in water and at pH = 5 and 8 was determined chromatographically.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2012년도 제43회 하계 정기 학술대회 초록집
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• pp.221-221
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• 2012

Small-molecule organic photovoltaic cells have recently attracted growing attention due to their potential for the low-cost fabrication of flexible and lightweight solar modules. The PVP/Ag nanoparticles were synthesized by the reaction of poly vinylpyrrolidone (PVP) and silver nitrate at $150^{\circ}C$. In the reaction, the size of the nanoparticles was controlled by relative mole fractions between PVP and Ag. The PVP/Ag nanoparticles with various sizes were then spin coated on the patterned ITO glass prior to the deposition of the PEDOT:PSS hole transport layer. The scattering of the incident light caused by these incorporated nanoparticles resulted in an increase in the path length of the light through the active layer and hence the enhancement of the light absorption. This scattering effect increased as the size of the nanoparticles increased, but it was offset by the decrease in total transmittance caused by the non-transparent nanoparticles. As a result, the maximum power conversion efficiency, 0.96% which was the value enhanced by 14% compared to the cell without incorporation of nanoparticles, was obtained when the mole fraction of PVP:Ag was 24:1 and the size of the nanoparticles was 20~40 nm.

• Macromolecular Research
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• 제10권2호
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• pp.115-121
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• 2002

Synthesis of polymers with controlled thermosensitive properties was carried out by conventional radical copolymerization of N-isopropylacrylamide (NIPAAm) with N-vinylpyrrolidone (NVP) taken as a hydrophilic comonomer. Lower activity of NVP rather than NIPAAm was revealed by gravimetric and $^1$H NMR analysis. Thermosensitive properties of the copolymers were investigated. It was found that aqueous solutions of the copolymers undergo thermo-induced phase transition and become opaque, precipitate or gel with heating. After formation of the gels their significant contraction was observed at storage. Swelling degree and amount of expelled water were measured in dependence on the copolymer composition, temperature and ionic strength of environment medium and concentration of the solution. It was determined that in collapsed state gels exhibit quite high water content. According to physico-chemical properties of the copolymers observed they could be suitable for biomedical application as an injectable implant material.

• Bulletin of the Korean Chemical Society
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• 제27권9호
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• pp.1346-1352
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• 2006

We describe an effective method of microchip electrophoresis (ME) based on single strand conformation poly-morphism (SSCP) analysis to rapidly detect the point mutation, Leu72Met, in a human obesity gene. The 207-bp dsDNA in the Leu72Met region, an estimate of the child obesity DNA mutant, was amplified by polymerase chain reaction (PCR) and submitted to a conventional glass microchip analysis with a sieving matrix of 1.75% poly(vinylpyrrolidone) (Mr 1 300 000), 1.0% poly(ethyleneoxide) (Mr 600 000) and 5.0% w/w glycerol. When combined with base stacking (BS) with hydroxide ions, the SSCP-ME provided rapid analysis as well as sensitive detection. The detection sensitivity was effectively enhanced in the OH- concentration range of 0.01-0.025 M NaOH. The sensitivity and speed of this ME-based SSCP methodology for the rapid detection of Leu72Met point mutations makes this an attractive method for diagnosing childhood obesity in a clinical diagnostic laboratory.

• 폴리머
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• 제25권5호
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• pp.728-735
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• 2001

본 연구에서는, $^{60}cO$ 방사선 (${\gamma}$-rays) 가교를 이용하여 PVA/키토산과 PVP/키토산의 혼합물로부터 하이드로겔을 제조하였다. 하이드로겔이 상처 치료용 드레싱으로 사용될 수 있는지 예측하기 위해 겔화율, 팽윤도, 겔강도같은 기계적 성질을 측정하였다. PVA와 키토산 및 PVP와 키토산의 비는 97 : 3 ~ 90 : 10이고, PVA/키토산 및 PVP/키토산 용액의 고형분의 농도는 15wt% 이었다. 하이드로겔의 기계적 성질에 조사선량이 미치는 영향을 예측하기 위해 PVA/키토산 및 PVP/키토산 혼합물에 25~70kGy의 감마선을 조사하였다. 겔화율과 겔강도는 키토산 조성비가 작을수록, 조사선량이 커질수록 증가하였다 팽윤도는 키토산 조성비가 클수록, 조사선량이 작을수록 증가하였다.

• 대한화학회지
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• 제48권5호
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• pp.483-490
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• 2004

시판 중인 poly(vinylpyrrolidone) (PVP)와 hydroxy ethyl cellulose (HEC) 혼합물을 충진젤 기질로 이용하여 한국 재래산양에 감염된 orf virus (ORFV)를 빠른 시간에 검출하여 진단할 수 있는 새로운 효소중합연쇄반응 (polymerase chain reaction, PCR)-마이크칩젤 전기영동법 (microchip gel electrophoresis, MGE)을 개발하였다. Orf 바이러스 B2L 유전자에서 지표-DNA인 594-bp DNA를 PCR로 증폭시킨 뒤, MGE법을 이용하여 증폭된 DNA를 분석하였다. MGE법은 64 mm 총길이(유효길이 36 mm) ${\times}$90 ${\mu}$m 폭 ${\times}$20 ${\mu}$m 깊이의 유리로 제작된 마이크로칩을 사용하였다. 1.0% PVP ($M_r$ 360,000)와 1.0% HEC ($M_r$ 250,000)의 혼합 충진젤과 277.8 V/cm의 전기장에서 4분 안에 증폭된 594-bp DNA를 분석하였다. PVP와 HEC의 혼합된 충진젤을 사용시 DNA 단편의 길이에 영향이 없이 하나의 DNA 피크를 나타내며 향상된 분리도와 이동시간의 재현성을 보여주었다. 본 PCR-MGE법은 고전적인 슬랩젤 전기영동법에 비해 약 20배 이상의 빠른 검출시간과 정량분석이 가능한 효과적인 ORFV 유전자단편 검출법이었다.