• 한국응용과학기술학회지
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• 제27권2호
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• pp.99-106
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• 2010

We have investigated the rheological behaviours of emulsions containing polymers. The polymers used in this study were polyacrylamide and carboxy vinyl polymer. The emulsion with polyacrylamide shows better prior preference than that with carboxy vinyl polymer on the skin texture. In the toxicity test, such as, LLNA cell toxicity, skin organ culture and human patch test, polyacrylamide was the appropriate materials for the cosmetics. The viscosity of polyacrylamide shows maximum value in neutral pH and good stability against temperature. The decreasing effect of viscosity against salt was not good enough but showed a better result than that of carboxy vinyl polymer. Two times the amount of polyacrylamide should be used for the formation of a similar viscosity of carboxy vinyl polymer. Yield value of polyacrylamide was low and the effect for the stabilizing emulsions was also low.

• 대한기계학회논문집
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• 제14권1호
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• pp.241-250
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• 1990

본 연구에서는 낙구식 점도계를 이용하여 낮은 농도의 용액을 실험할 때 종말 속도측정의 어려움을 해결하기 위하여 레이저와 특수 타이머를 설치하였으며 정확한 특성시간을 결정하기 위하여 실린더 내부의 시험유체를 교란시키지 않고, 떨어뜨린 구 를 회수하는 장치를 제작하였다. 또한 주로 rheogoniometer에 의존하던 영 전단률 점성계수를 측정하기 위하여 속이 빈 알루미늄 구(hollow aluminium ball)의 밀도를 시험 유체와 거의 같은 정도까지 변화시켜가며 종말 속도를 측정하였으며 점탄성 유체 로써 Separan AP-273의 낮은 농도인 300에서 2000wppm까지의 저농도 용액에 대한 특성 시간을 여러모델에 의하여 실험적으로 결정하고 저농도 폴리머 용액에서 퇴화로 인한 점탄성유체의 특성 변화를 분석하였다.

• 폴리머
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• 제30권2호
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• pp.118-123
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• 2006

폴리(부틸렌 테레프탈레이트)(PBT)와 폴리(에틸렌 테레프탈레이트)(PET)의 용융 가공시 발생하는 상호에스테르 교환반응이 PBT/PET 블렌드의 유변 물성에 미치는 영향에 대하여 살펴보았다. PBT에 PET를 용융 블렌딩하면 PET의 상대적인 낮은 점도에 의하여 PET의 함량이 증가할수록 PET의 점도가 감소됨을 알 수 있었으며 이와 함께 용융가공시 발생하는 분자량 감소와 PBT와 PET 상호간에 발생하는 상호에스테르 교환반응에 의하여 추가적인 용융점도 감소가 있음을 확인하였다. 또한 PBT와는 달리 윤활제로 사용한 calcium stearate(CaST)는 PBT/PET 블렌드에서 윤활 작용은 미약한 반면 이들 블렌드의 열분해에 따른 분자량 감소와 상호에스테르 교환반응을 촉진하여 추가적인 용융점도 감소를 초래함을 알 수 있었다.

• 한국섬유공학회:학술대회논문집
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• 한국섬유공학회 2003년도 The Korea-Japan Joint Symposium
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• pp.101-101
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• 2003

TLCP/Polyester binary blends were prepared by melt blending. Rheological, morphological, and thermal properties of of TLCP/polyester blends were investigated with viscosity ratio. Diameter of TLCP fibrils decreased with viscosity ratio. More and smaller TLCP fibrils were obtained at higher shear rate. Lower viscosity ratio was necessary for the fibrillation of TLCP in the binary blends.

• Bulletin of the Korean Chemical Society
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• 제16권11호
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• pp.1046-1056
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• 1995

A topological theory has been introduced to evaluate the degree of complexation and the viscosity of polymer complexes by extending the theory of Iliopoulos and Audebert for aqueous polymer solutions. The previous theory of Iliopoulos and Audebert has offered only a semiquantitative theoretical model for polymer complex systems, whereas our present work gives a general theoretical model applicable to all the polymer complex systems. Their theories considered only the physical property term caused by the displacement of complexed points between polymer solute chains, while our theory deals with all the physical effects, caused by the displacement of complexed points entangled points in polymer solute chains. There have been predicted the characteristics of physical properties from the expression. It is exposed that the predictive values show good agreement with the experimental data for polymer complexes.

• 한국산학기술학회논문지
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• 제11권3호
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• pp.1023-1026
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• 2010

이 논문에서는 미세한 통로를 흐르는 고분자 블렌드의 유변학적 특성에 관하여 연구하였다. 우선 두께가 각각 0.1, 0.2 0.5 mm 인 세 종류의 슬릿 다이를 제작하였고 특수 제작한 피스톤을 부착한 모세관 점도계로 고분자 블렌드의 점도 거동을 관찰하였다. 관찰 결과 상구조가 해도 구조를 가지는 경우 고분자 블렌드의 점도는 다이의 크기에 의존하지 않음을 알 수 있었다. 그러나 상구조가 co-continuous 구조를 가지는 경우에는 점도가 다이의 크기에 의존함을 관찰하였는데, 몇몇 부가 실험 결과 이는 각 상 간의 미끄러짐이 원인임을 알 수 있었다.

• Macromolecular Research
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• 제16권3호
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• pp.218-223
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• 2008

In order to obtain crosslinked poly(butylene succinate) (PBS) foams with a closed-cell structure, a commercial-grade PBS was first modified in the melt using two different branching agents to increase the melt viscosity. The rheological properties of the branched and crosslinked PBS were examined by varying the amount of the branching agents. The complex viscosity of the crosslinked PBS increased with increasing amount of the branching agent. However, it decreased with increasing frequency. When 2 phr of the branching agent was added to PBS, the storage modulus (G') was higher than the loss modulus (G") throughout the entire frequency range, showing that the addition of a branching agent increases the melt viscosity and elasticity of PBS effectively. Closed-cell PBS foams were prepared by mixing the chemical blowing agent with the crosslinked PBS. The effect of the foaming conditions such as temperature and time, and the amount of the crosslinking agent on the structure of the expanded PBS foams were also investigated.

• Korea-Australia Rheology Journal
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• 제14권4호
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• pp.189-201
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• 2002

The interaction between hydrophobically modified hydroxyethyl cellulose (hmHEC), containing approximately 1 wt% side-alkyl chains of $C_{16}$, and an anionic sodium dodecyl sulphate (SDS) surfactant was investigated. For a semi-dilute solution of 0.5 wt% hmHEC, the previously observed behaviour of a maximum in solution viscosity at intermediate SDS concentrations, followed by a drop at higher SDS concentrations, until above the cmc of surfactant when the solution resembles that of the unsubstituted polymer, was confirmed. Additionally, a two-phase region containing a hydrogel phase and a water-like supernatant was found at low SDS concentrations up to 0.2 wt%, a concentration which is akin to the critical association concentration, cac, of SDS in the presence of hmHEC. Above this concentration, SDS molecules bind strongly to form mixed micellar aggregates with the polymer alkyl side-chains, thus strengthening the network junctions, resulting in the observed increase in viscosity and elastic modulus of the solution. The shear behaviour of this polymer-surfactant complex during steady and step stress experiments was examined In great detail. Between SDS concentrations of 0.2 and 0.25 wt%, the shear viscosity of the hmHEC-polymer complex network undergoes shear-induced thickening, followed by a two-stage shear-induced fracture or break-up of the network. The thickening is thought to be due to structural rearrangement, causing the network of flexible polymers to expand, enabling some polymer hydrophobic groups to be converted from intra- to inter-chain associations. At higher applied stress, a partial local break-up of the network occurs, while at even higher stress, above the critical or network yield stress, a complete fracture of the network into small microgel-like units, Is believed to occur. This second network rupture is progressive with time of shear and no steady state in viscosity was observed even after 300 s. The structure which was reformed after the cessation of shear is found to be significantly different from the original state.

• 대한기계학회:학술대회논문집
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• 대한기계학회 2004년도 춘계학술대회
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• pp.1114-1119
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• 2004

In a foaming process of microcellular plastics (MCPs) with a injection molding, research on the viscosity change that occurs when the gas is injected to the polymer has received little attention despite its importance. The purpose of this paper is to provide the basic data required to determine the processing condition by measuring viscosity changes against the gas injection rates of the blowing agent, and to verify the influence of the viscosity change on the flow condition of polymer inside the mold at the injection process.

• Bulletin of the Korean Chemical Society
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• 제21권9호
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• pp.875-881
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• 2000

We study the rheological properties of concentrated polymer solution and the melt under simple shear and elon-gational flow using Brownian dynamicssimulation. In order to describe the anisotropic molecular motion, we modifiedthe Giesekus' mobility tensor by incorporating the finitely extensible non-linear elastic (FENE) spring force into dumbbell model. To elucidate the nature of this model, our simulation results are compared with the data of FENE-P ("P"standsfor the Perterin) dumbbell model and experiments. While in steady state both original FENE and FENE-P models exhibit a similar viscosity response,the growthof viscosity becomes dissimilar as the anisotropy decreases and the flowrate increases. The steady state viscosity obtained from the simulation well describes the experiments including the shear-thinning behavior in shear flow and viscosity-thinning behavior in elongational flow. But the growth of viscosity oforiginal FENE dumbbell model cannot describe the experimental results in both flow fields.