• 폴리머
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• 제26권4호
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• pp.535-542
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• 2002

투석법을 이ctide-co-glycolide) (PLGA) 나노입자를 제조하고 다양한 용매에 따른 입자 크기, 약물 함유량, 생분해도 등과 같은 물리ㆍ화학적 특성을 조사하였다. Dimethylacetamide (DMAc), dimethylformamide (DMF), dimethylsulfoxide (DMSO)로 제조된 PLGA 나노입자의 크기는 acetone으로 제조한 입자보다 적었다. 또한, 약물 함유량은 DMAc>DMF>DMSO=acetone 순서였다. PLGA 나노입자는 scanning electron microscopy (SEM)과 transmission electron microscopy (TEM)의 측정으로 구형임을 알 수 있었다. 계면활성제를 사용하지 않는 나노입자에 봉입된 norfloxacin (NFx)은 X-ray diffraction 분석을 통하여 입자 표면에 약물을 가지지 않는 좋은 약물 봉입 효율을 가짐을 알 수 있었다. 모델약물로 사용된 NFx의 방출속도는 약물 함유량뿐만 아니라 입사크기에 의해 좌우된다. 또한 PLGA 나노입자의 분해속도는 아세톤보다는 DMF를 사용하였을 때 더 빠르며 이는 PLGA 나노입자의 생분해성도 입자크기에 좌우된다는 것을 알 수 있었다.

• Membrane and Water Treatment
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• 제11권4호
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• pp.237-245
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• 2020

The effects of the mixed two solvents, Dimethylacetamide (DMAc) and Dimethylformamide (DMF), and Polyethylene glycol (PEG) and Polyvinylpyrrolidone (PVP) as additives on performance of Polyvinylidene fluoride (PVDF) membranes were studied. Initially, PEG200 was used as a primary additive at fixed percentage of 5% wt. PVP was then blended with PEG200 in different concentrations. PVDF and DMAc were used as polymer and solvent in the casting solutions, respectively. To control the diffusion rate of PVP in the presence of PEG200 and PVP blend, mixtures of DMAc and DMF were used as the mixed solvent in the casting solutions. Asymmetric PVDF membranes were prepared via phase inversion process in a water bath and the effects of two additives and two solvents on the membrane morphology, pure water flux (PWF), hydrophilicity and rejection (R) were investigated. Attenuated Total Reflection Fourier Transform Infrared Spectra (ATR-FTIR) analysis was used to show the residual PVP on the surface of the membranes. Atomic Force Microscopy (AFM) was utilized to determine roughness of membrane surface. The use of mixed solvents in the casting solution resulted in reduction of PVP diffusion rate and increment of PEG diffusion rate. Eventually, PWF and R values reduced, while porosity and hydrophilicity increased.

• 한국염색가공학회지
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• 제15권2호
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• pp.68-75
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• 2003

In this work, ultrafiltration(UF) membranes were prepared using polyethersulfone(PES). The polymer was dissolved in various solvent, such as N, N-dimethyl formamide(DMF), N,-dimethyl acetamide (DMAc), N,N-dimethyl sulfoxide(DMSO) and N-methyl-2- pynolidone(NMP). Each polymer solution was casted on the glass plate, and immersed into non-solvent bath. In this way finely porous UF membranes were prepared by phase inversion method. The cross sectional structure of PES membrane was asymmetric which was consist of sponge-like sublayer, finger-like toplayer, and active skin layer. From the solute rejection experiments, the molecular weight cut off of the prepared membrane in various solvent was evaluated 10,000 for DMF, 30,000 for DMAc, 50,000 for DMSO, and 10,000 for NMP respectively.

• 통합자연과학논문집
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• 제8권4호
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• pp.235-243
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• 2015

Rhodium(I)-complex of $[Rh(CO)_2I_2{^-}]$ catalyzed carbonylation of anhydrous-trimethylamine in the presence of methyl iodide to give DMAC (N,N-dimethylacetamide) in no solvent. The catalyst had been reused 20 times, the analyses and distillation of collected products showed that the yields of DMAC, MAA (N-methylacetamide), and DMF (N,N-dimethylformamide) were 82.3%, 12.6%, and 4.4%. The conversion rate of trimethylamine was 99 % and the selectivity of DMAC was 82.3% with TON (Turnover Number) of 700. Stepwise procedure of inner-sphere reductive elimination for the formation of DMAC was suggested instead of acyl iodide intermediate.

• 멤브레인
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• 제23권1호
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• pp.80-91
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• 2013

$Fe(SO_4)_2$, cyclohexanedione dioxime, phenylboronic acid을 이용하여 금속 템플레이트 중합을 실시한 후 메탄올로 세척하여 Fe(II) clathrochelate 화합물을 합성하였다. Fe(II) clathrochelate와 polyethersulfone을 이용한 유무기 복합 멤브레인을 제조하였다. 멤브레인 제조를 위하여 Fe(II) clathrochelate는 DMF, NMP, DMAC와 같은 멤브레인 제조에 이용되는 극성 아프로틱 용매에 잘 녹는 물질로 고안되었다. Fe(II) clathrochelate는 trifluorosactic acid와 같은 강산 존재하에서도 금속이 분리되지 않고 안정성이 유지되었다. UV-vis 분광법으로 용액 가용성을 확인하였으며 (i) 강산 및 (ii) 경쟁 킬레이트제를 이용하여 용액상의 안정성을 확인하였다. 유무기 복합막은 PES, PVP, TSA, Fe(II) clathrochelate를 DMF에 녹여 NIPS (비용매 유도 상전이) 방법으로 제조하였다. Fe(II) clathrochelate의 첨가는 표면의 기공 밀도의 향상, 평균기공 크기의 증가 및 유량 증가에 영향을 주었으며 상대적으로 비대칭 구조를 가지는 성능이 향상된 멤브레인을 얻을 수 있었다.

• Elastomers and Composites
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• 제50권2호
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• pp.138-145
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• 2015

A series of wholly aromatic poly(hydroxyamide)s(PHAs), containing varying amounts of 2,6-dimethylphenoxy group and quinoxaline ring in the main chain, were synthesized by a direct polycondensation method. The inherent viscosities of the PHAs in either DMAc or DMAc/LiCl solution at $35^{\circ}C$ were found to be in the range of 1.02~1.90 dL/g. In the solubility study, we observed that PHA 1, PHA 2, and PHA 3 were dissolved in aprotic solvents such as DMAc, NMP, DMF, and DMSO with LiCl on heating; however, PHA 4, PHA 5, and PHA 6 could be dissolved in aprotic solvents on heating without LiCl. For poly(benzoxazole)s(PBOs), the 10% and maximum weight loss temperatures were in the range of $582{\sim}622^{\circ}C$ and $630{\sim}659^{\circ}C$, respectively. Residues of PBOs at $900^{\circ}C$ were found to be relatively high, which were in the range of 65.3~70.8%.

• Elastomers and Composites
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• 제50권3호
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• pp.175-183
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• 2015

A series of fluorinated aromatic poly(hydroxyamide)s (PHAs) were synthesized by direct polycondensation of diacides containing 2,6-dimethylphenoxy group and quinoxaline ring in the main chain with 2,2-bis-(3-amino-4-hydroxyphenyl) hexafluoropropane. The PHAs had relatively low inherent viscosities in the range of 0.35~0.43 dL/g at $35^{\circ}C$ in DMAc solution. All PHAs exhibited excellent solubility in aprotic solvents such as NMP, DMAc, DMF and DMSO as well as in common organic solvents such as pyridine, THF, and m-cresol at room temperature. However, the poly(benzoxazole)s (PBOs) were quite insoluble in all organic solvents except partially soluble in concentrated sulfuric acid. The PBOs showed glass transition temperatures between 233 and $284^{\circ}C$ by DSC and maximum weight loss temperatures in the range of $536-546^{\circ}C$ by TGA.

• Elastomers and Composites
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• 제54권4호
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• pp.321-329
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• 2019

A series of poly(hyroxyamide)s (PHAs) was prepared by direct polycondensation reaction of 4,4'-(2,3-pyridinedioxy)dibenzoic acid and/or isophthalic acid with 3,3'-dihydroxybenzidine. The yield percentages of the products were high, and the inherent viscosities of the polymer in DMAc solution at 35℃ were 0.31-0.59 dL/g. All PHA polymers were found to be soluble in polar aprotic solvents such as DMAc, DMSO, NMP, and DMF. On the other hand, LiCl was required to dissolve IPHA-1 in aprotic solvents. Poly(benzoxazole)s (PBOs) were partially soluble in conc-H₂SO₄; IPBO-4, -5, and -6 were partially soluble in NMP only when LiCl was added to the solution, and the solution was heated. The PBO polymers showed a maximum weight loss in the temperature range of 654-680℃, and the char yields at 900℃ under nitrogen atmosphere exceeded 63%.

• Elastomers and Composites
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• 제46권4호
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• pp.295-303
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• 2011

3,3'-dihydroxybenzidine 과 2,2-bis (3-amino-4-hydroxyphenyl)hexafluoro-propane을 포함하는 두가지 타입의 bis(o-aminophenol)s 과 imide-diacids 를 직접 축 중합하여 imide 고리를 포함한 새로운 방향족 polyhydroxyamides(PHAs)을 합성하였다. 모든 중합체들은 FT-IR, FT-NMR, DSC 및 TGA를 이용하여 조사하였다. 중합체들의 고유점도는 $35^{\circ}C$의 DMAc 용액에서 측정하였으며, 0.49-1.13 dL/g 을 보였다. PHA 1을 제외한 PHA 2 와 3은 DMF, DMAc, NMP 등 극성 용매에 잘 용해되었으며, 6F 그룹이 포함된 PHA 4, 5, 및 6은 극성이 낮은 용매에 대해서도 좋은 용해도를 보였다. 반면에 polybenzoxazoles(PBOs)은 황산에 일부 용해되는 것 외에 다양한 용매에도 용해되지 않았다. 질소분위기 하에서 PBO 1, 2, 3의 최대 열분해온도는 $650-656^{\circ}C$ 범위의 값들을 보였고, char 수득율도 57.4-61.9 %로 비교적 높은 값을 보였다. 이로부터 고분자 주 사슬에 imide 혹은 diimide 고리의 도입은 PHA 혹은 PBO의 열안정성을 높이는데 효과적임을 알 수 있었다.

• Elastomers and Composites
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• 제42권4호
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• pp.238-248
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• 2007

일련의 방향족 polyhydroxyamides(PHA)를 저온 용액 중축합으로 합성하였다. 이들 중합체들은 FT-IR, $^1H-NMR$, DSC, TGA 그리고 PCFC를 이용하여 특성들을 조사하였다. PHA 중합체들의 고유점성도는 DMAc 용매 하에 $35^{\circ}C$에서 $0.5{\sim}1.1dL/g$의 값을 나타내었다. PHA 3을 제외한 중합체들은 N,N-dimethylacetamide(DMAc), N-methyl-2-pyrrolidone(NMP), N,N-dimethylformamide(DMF) 등과 같은 극성 유기 용매에 용해되었지만, 열적 고리화 반응에 의해 전환된 polybenzoxazoles(PBOs)는 용해되지 않았다. PBO 3을 제외한 PBO 중합체들에서는 DSC에서 $200{\sim}246^{\circ}C$의 유리전이온도($T_g$)를 보였고, TGA에서의 최대분해온도는 질소 분위기 하에서 $597{\sim}697^{\circ}C$의 범위를 보였다. PBO 중합체들은 $51{\sim}64%$의 높은 차 수득률을 보였다. PCFC에서 PBOs의 heat release(HR) capacity는 $8{\sim}65J/gK$의 값을 보였고, total heat release(total HR)의 값은 $2.4{\sim}4.7kJ/g$을 보였다.