• 공업화학
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• 제5권5호
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• pp.878-888
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• 1994

ABS 수지의 파단 거동을 살펴 보기 위해 rubber content, molecular weight, lubricant의 종류 및 양과 파단 speed, 주위 환경온도를 변수로 측정한 후 전자현미경 사진으로 그 파단면을 살펴 보았다. Tension하에서 rubber content와 lubricant content는 감소할수록, molecular weight와 tension speed는 증가할수록 strength는 증가하였으며, 파단면은 rubber content, speed, molecular weight는 감소할수록, liquid lubricant를 사용할수록 파단부위 주변의 변형이 일어나지 않았으며, 파단면도 수지가 서로 미끄러져 파단되는 상태가 아닌 상분리와 같은 형상으로 분리파단되었다. Impact하에서 rubber content, molecular weight, 주위 환경온도, lubricant content가 증가할수록 strength도 증가하였으며, 파단면은 사진상의 파단표면적이 작은 것이 높은 strength를 나타내고 있다.

• Elastomers and Composites
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• 제24권1호
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• pp.11-18
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• 1989

The thermal degradation of Poly(methyl methacrylate) (PMMA) and poly(acrylonitrile butadiene styrene)(ABS) terpolymer as well as their mixtures were carried out using the thermogravimetry and differential scanning calorimetry(DSC) in the stream of nitrogen and air with 50 ml/min at the various heating rate from 4 to $20^{\circ}C/min$ and temperature from 200 to $300^{\circ}C$ The values of activation energies of thermal degradation determined by TG and DSC in the various PMMA/ABS mixtures were $34{\sim}58Kcal/mol,\;35{\sim}54Kcal/mol$ in the stream of nitrogen. The values of activation energy of ABS20% mixture was appeared high in camparison with addition rule. According to increasing the composition of ABS, the temperatures of glass transition and initial decomposition temperature were increased. PMMA/ABS mixtures by the analysis of infrared spectrophotometer were decomposed by main chain scission in the stream of nitrogen.

• Macromolecular Research
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• 제9권1호
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• pp.30-36
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• 2001

Polybutadiene latex grafted (g-PB) in g-PB/SAN blends, i.e., acrylonitrile-butadiene-styrene terpolymer (ABS) were partially replaced by acrylonitrile-butadiene copolymer (NBR) with various acrylonitrile (AN) contents. Changes in morphology, physical and rheological properties were examined. The dispersed size of NBR was decreased as the miscibility with matrix SAM, was increased by increasing AN content in NBR upto 50 wt%. Impact strength was enhanced about two-fold due to the NBR dispersed with a slight larger size than the original g-PB. Gloss was effectively reduced as the particle size of NBR was increased. Tensile yield strength was decreased, and elongation at break or yield behavior at low shear rate were increased as g-PB was partially replaced by NBR having AN content less that 40 wt%.

• 폴리머
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• 제28권3호
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• pp.263-272
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• 2004

자동차 계기판을 제조하는 기체 사출 성형의 공정에 있어서 전산 모사를 통한 공정성 및 제조된 제품의 물성 향상에 관한 연구를 수행하였다. ABS 삼원공중합체의 P-V-T 자료를 이용하여 기체 사출 공정을 적용하였으며 시간에 따른 금형 충전 효과를 예측하였다. 또한 기체 사출 성형에 있어서 압력, 충전 시간, 기체의 주입 통로 및 런너의 위치 등 다양한 가공 인자들을 변화시킴으로서 공정의 최적 조건을 찾을 수 있었다. 이러한 전산 모사를 통하여 확립된 공정을 통해 제조된 계기판은 일반적인 사출 성형법에 의해 제조되어진 제품에 비해서 우수한 치수 및 변형 안정성이 개선되었다.

• Elastomers and Composites
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• 제24권2호
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• pp.110-121
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• 1989

The radical initiated graft copolymerization of acrylonitrile(AN) and 4-chlorostyrene(4-Clst) onto ethylene-propylene-diene terpolymer(EPDM) rubber was investigated under various conditions. Graft copolymer(AU-EPDM-4-Clst) was isolated b: selective solvent extraction and identified by using IR spectroscopy. The percent grafting is determined as a function of solvent, reaction time, and monomer mole ratio. Percent grafting decreased in the order of tetrahydrofuran(THF)>THF/ethyl acetate(EA)(1 : 1)>cyclohexane/EA(1 : 1)>n-hexane/EA(1 : 1). Grafting increased continuously with increasing the reaction time up to 40 hr, beyond which the grafting levelled off. It was observed that percent grafting increased as increasing [4-Clst]/[AN] mole ratio, but decreased when [4-Clst]/[AN] mole ratio was higher than 1.60. The light resistance of graft copolymer(AN-EPDM-4-Clst) was better than that of ABS.