• 멤브레인
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• 제14권3호
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• pp.250-257
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• 2004

이산화탄소 분리에 이용하기 위하여 PEG (Poly(ethylene glycol)diacrylate)와 PPG (Poly(propylene glycol) diacrylate)를 광학 중합반응(Photopoly merization)을 이용하여 제조하였다. PEG와 PPG는 분자량이 각각 258과 540이었다. PEG와 PPG의 질량 혼합비(wt%)를 9:1, 8:2, 7:3, 6:4, 5:5로 변화시키면서 막을 제조하였다. $25^{\circ}C$에서 PEG/PPG (9:1)의 이산화탄소 투과도는 28.9 barrel 으로 나타났으며, 선택도($PCO_2$/$PN_2$)는 57.9로 나타났다. 같은 온도에서 PEG/PPG(5:5)로 조성을 변화시켰을 때 이산화탄소 투과도는 40.4 Barrer, 기체선택도($PCO_2$/$PN_2$)는 51.8를 나타냈다 이산화탄소의 투과도는 5:5 > 6:4 > 7:3 > 8:2 > 9:1의 경향을 나타내었다. $35^{\circ}C$로 승온을 하는 경우에 PEG/PPG (9:1)는 45.4 Baller, 선택도($PCO_2$/$PN_2$)는 48.2을 나타냈으며, PEG/PPG (5:5)의 이산화탄소 투과도는 78.9 Barrer을 나타내고 선택도($PCO_2$/$PN_2$)는 33.2로 나타났다. 각각의 온도에서 이산화탄소의 기체선택도($PCO_2$/$PN_2$)는 PPG의 함량이 증가하면서 감소하는 경향을 나타내었다.

• 청정기술
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• 제17권3호
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• pp.244-249
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• 2011

이산화탄소/프로필렌 옥사이드 공중합을 통하여 고분자 사슬 내에 친수성기와 소수성기가 공존하는 저분자량의 블록 공중 합체를 합성하였다. 고활성의 촉매를 사용한 이산화탄소/프로필렌 옥사이드 공중합 반응에 단말기로 -OH기를 갖는 폴리(에틸렌 글리콜)(PEG)을 분자량 조절제로 투입하여 블록 공중합체를 합성하였다. 단말기 한쪽 끝에만 -OH기를 갖는 폴리(에틸렌 글리콜)을 투입하였을 때는 PEG-block-PPC (폴리(프로필렌 카보네이트)) 다이블록 공중합체가 얻어지고, 단말기 양쪽 끝 모두 -OH기를 갖는 폴리(에틸렌 글리콜)을 투입하였을 때는 PPC-block-PEG-block-PPC 트리블록 공중합체가 얻어진다. 제조된 블록 공중합체는 $^1H$-NMR 스펙트럼을 통하여 구조 분석을 하였고 GPC를 통하여 분자량을 측정하였다.

• 폴리머
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• 제39권2호
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• pp.247-255
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• 2015

Poly(1,2-propylene glycol adipate) (PPA) was used as an environmentally friendly plasticizer in flexible poly(vinyl chloride) (PVC). Thermal, mechanical, and rheological properties of the PVC/PPA blends were characterized by differential scanning calorimetry, dynamic mechanical analysis, tensile test, scanning electron microscopy and small amplitude oscillatory shear rheometry. The results showed that PPA lowered the glass transition temperature of PVC. The introduction of PPA could decrease tensile strength and Young's modulus of the PVC/PPA blends; however, elongation-at-break was dramatically increased due to the plastic deformation. The plasticization effect of PPA was also manifested by the decrease of dynamic storage modulus and viscosity in the melt state of the blends. The results indicated that PPA had a good plasticizing effect on PVC.

• 폴리머
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• 제30권2호
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• pp.152-157
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• 2006

수산기말단 폴리부타디엔(hydroxy-terminated polybutadiene: HTPB) 폴리올을 이용한 수분산 폴리우레탄(water-home polyurethane: WPU)의 제조에서 HTPB와 poly(propylene glycol)(PPG)을 혼합 사용한 음이온계 WPU와 쯔비터이온계 WPU를 제조하고 이들의 특성을 조사하였다. WPU 제조 시 HTPB 함량이 증가하면 입자 크기는 커지는 경향을 보이고, 폴리우레탄의 연질부와 경질부의 상분리는 증가하였다. 음이온계 WPU에 비하여 쯔비터이온계 WPU는 건조 필름의 분자간 수소 결합이 강해지는 경향을 나타내었다. 음이온계 및 쯔비터이온계 WPU는 공통적으로 건조 필름이 HTPB 함량이 폴리올 중 25 wt%일때 실험 범위에서는 신율과 인장 강도가 최대값을 보였으며, 이러한 특성은 폴리우레탄의 연질부와 경질부 사이의 미세 상분리를 반영한 것으로 판단되었다.

• Elastomers and Composites
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• 제27권3호
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• pp.161-173
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• 1992

A series of polyurethane block copolymers based on hydroxyterminated poly(dimethyl siloxane), poly(propylene glycol) and poly(tetramethylene glycol) soft segments of molecular weights 1,809, 2,000 and 2,000, respectively, were synthesized. The hard segments consisted of 4,4'-diphenylmethane diisocyanate and 1,4-butanediol as the chain extender. Samples with different molar ratios were prepared. We tried to synthesize poly(dimethyl siloxane)-based polyurethane(PDMS-PU) containing a hard block as major fraction and a soft block as minor fraction for preparing toughened rigid systems. After a study of the pure PDMS-PU, poly(propylene glycol)-based polyurethane(PPG-PU) and poly(tetramethylene glycol)-based polyurethane(PTMG-PU), (mixed polyol)-based block copolymers and blends between PDMS-PU, PPG-PU and PTMG-PU were prepared, and characterized by means of differential scanning calorimetry, tensile testing and scanning electron microscopy. In (mixed polyol)-based PU and in lower hard segment content blends, macro-phase separation was shown, but blends with higher hard segment contents showed significant reduction in amounts of phase separation.

• Macromolecular Research
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• 제17권8호
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• pp.591-596
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• 2009

To trace the plasticizing effects of propylene glycol (PG) on poly(vinyl alcohol) (PVA), the rheological properties of PVA solutions in dimethyl sulfoxide (DMSO) and the physical properties of PVA films were discussed in terms of PG content. Both properties were closely related to the hydrogen bond breaking effects of PG The 6 and 12 wt% PVA solutions containing PG exhibited Bingham behavior, which was more noticeable at lower plasticizer content and higher polymer concentration. The 6 wt% PVA solutions containing more than 30 wt% PG showed a sudden decrease of viscosity over the frequency range of 0.08 and 0.2 rad/s. However, the 12 wt% PYA solutions showed no viscosity reduction even at a PG content up to 40 wt%. The glass transition temperature of the PVA/PG films was almost linearly decreased with increasing PG content but an abrupt reduction was observed at a plasticizer content 30 wt%, suggesting that the hydrogen bond breaking effects of PG on PVA became dominant between 20 and 30 wt%. This effect was further supported by the similar tendency of the tensile properties.

• 폴리머
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• 제39권3호
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• pp.461-467
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• 2015

본 논문은 ferric p-toluenesulfonate를 산화제에 약 염기인 이미다졸과 poly(ethylene glycol)-poly(propylene glycol)-poly(ethylene glycol) (PEG-PPG-PEG) 계면활성제를 동시 첨가하여 기상중합법으로 제조된 poly(3,4-ethylenedioxythiophene) (PEDOT) 박막의 광-전기적 특성 향상에 대한 것이다. 여러 가지 조건에서 제조된 PEDOT 박막 특성과 산화제의 첨가제로 사용된 약 염기와 계면활성제의 조합 효과의 상관관계를 규명하고자 하였다. 이미다졸과 PEG-PPG-PEG로 구성된 첨가제를 사용하여 제조된 PEDOT 박막은 $1300S{\cdot}cm^{-1}$ 이상의 전도성을 가졌다. PEG-PPG-PEG계 계면활성제의 분자량이 기상 중합을 이용한 PEDOT 박막의 특성에 미치는 영향도 조사하였다.

• Journal of Pharmaceutical Investigation
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• 제33권1호
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• pp.45-49
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• 2003

The solubility and stability of ondansetron hydrochloride (OS) in various vehicles were determined. The effect of cyclodextrins (CD) on the solubility of OS in water was determined by equilibrium solubility method. The solubility of OS at $32^{\circ}C$ increased in the rank order of isopropyl myristate (IPM) < propylene glycol laurate (PGL) ${\ll}$ propylene glycol monolaurate < propylene glycol monocaprylate (PGMC) < poly(ethylene glycol) 400 < diethylene glycol mono ethyl ether (DGME) < ethanol < poly(ethylene glycol) 300 < water (36.1 mg/ml) ${\ll}$ propylene glycol (PG) (283 mg/ml). The addition of PG or DGME to non-aqueous vehicles such as IPM, PGL and PGMC markedly increased the solubility of OS. The addition of CDs in water increased the solubility. Apparent stability constant for the CD complexation with OS was calculated to be $25.5\;M^{-1}$ for $2-hydroxypropyl-{\beta}-CD\;(2HP{\beta}CD)$. Twenty mM ${\beta}-CD$, 69.4 mM sulfobutyl ether ${\beta}-CD$ and 115.4 mM $2HP{\beta}CD$ increased the aqueous solubilty of OS 1.27, 2.18 and 1.85 times, respectively. OS was stable in buffered aqueous solution (pH 5.0). However, OS was relatively unstable in non-aqueous vehicles in the order of PG

• Macromolecular Research
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• 제9권6호
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• pp.332-338
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• 2001

Waterborne polyurethane as a new polymer electrolyte was synthesized by using relatively hydrophilic polyols. The morphology of polyurethane was changed as it was dispersed in water. In contrast to polyurethane ionomer, waterborne polyurethane did not form an ionic cluster but produced a binary system composed of hydrophilic and hydrophobic groups. In the colloidal system, the former and the latter existed at outward and inward, respectively. Waterborne polyurethane was prepared from poly(ethylene glycol) (PEG) /poly(propylene glycol) (PPG) copolymer, 4,4'-diphenylmethane diisocyanate(MDI), ethylene diamine as a chain extender, and three ionization agents, 1,3-propane sultone, sodium hydride and lithium hydroxide. PEG/PPG copolymer was used for suppressing the crystallinity of PEG and N-H bond was ionized for increasing the electrochemical stability of polyurethane. Low molecular weight poly(ethylene glycol) and poly(ethylene glycol dimethyl ether) (PEGDME) were used as plasticizers. DSC, FT-IR and $^1$H-NMR of the waterborne polyurethane were measured. Also, the ionic conductivity of solid polymer electrolytes based on waterborne polyurethane and various concentrations of low molecular weight poly(ethylene glycol) or PEGDME were measured by AC impedance.

• 폴리머
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• 제29권2호
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• pp.140-145
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• 2005

열가소성 폴리우레탄(thermoplastic polyurethane: TPU)의 제조에 사용한 폴리올 종류와 경질부 함량에 따른 TPU의 결정화 거동을 고찰하였다. TPU의 제조에 사용한 폴리올은 분자량이 2000인 poly(tetamethylene ether glycol) (PTMEG), poly(propylene glycol)(PPG) diol, polycaprolactone(PCL) diol, poly(butylene adipate)(PBA) diol을 사용하였으며, 경질부 함량은 $35\~44\;wt\%$였다. TPU의 경질부 냉각 결정화는 경질부 함량이 많을수록 고온에서 관찰되었다. TPU의 등온 결정화 속도는 경질부 함량이 많을수록 빠르고, TPU 제조에 사용한 폴리올 종류별로는 $PTMEG>PPG>PCI{\geqq}PBA$ 경향이 나타나, 연질부와 경질부의 상용성이 낮을수록 용융상태에서 경질부의 수소결합이 용이하고 결정화 속도가 빠르며, 냉각 결정화가 고온에서 나타나는 것으로 해석하였다.