• Journal of the Korean Chemical Society
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• v.23 no.5
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• pp.329-337
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• 1979

The water-vapour transmission ratios (WVTR) of the various commercial polymer films have been investigated at the constant pressure and relative humidity (RH). Water proofnesses, the reciprocals of WVTR for the various samples, were determined using a cup device and maintaining the sample films at a constant temperature ($40{\pm}1^{\circ}C$) and a constant R. H ($90{\pm}2%$) for 24 hours. The following order of the relative proofness was observed; oriented polypropyrene (O.PP) > high density polyethylene (HDPE, Inflation) > high density polyethylene (HDPE. T-die) > casted polypropylene (C. PP) > nonoriented polyester (N. PET) > low density polyethylene (LDPE) > oriented polyester (O. PET) > rigid polyvinyl chloride (Rigid PVC) > semirigid polyvinyl chloride (Semirigid PVC) > nonrigid polyvinyl chloride (Nonrigid PVC) > oriented nylon (O. Nylon) > nonoriented nylon (N. Nylon). And water proofness order was also observed to decrease with the temperature rising; HDPE (T-die) > C. PP > O. PET > LDPE > O. Nylon. The activation energies of LDPE, HDPE (T-die), C. PP, O. PET and O.Nylon films were 12.0, 11.1, 11.4, 11.7, 14.1 kcal/mole, respectively. The WVTR's of the films were increased with the polarity of polymer and the addition of plasticizer in PVC, decreased with the increase of the film thickness and mechanical orientation. The WVTR's of the laminated films O. PP/LDPE, N.Nylon/LDPE, C.PP/LDPE were also more dependent on the film thickness than the WVTR's of the single films.

• Proceedings of the Korean Society of Dyers and Finishers Conference
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• 2012.03a
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• pp.34-34
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• 2012

Polypropylene 섬유는 세계적으로 큰 관심을 모으고 있는 섬유 소재로 환경친화성, 경량성, 신축성 등 다양한 기능성을 보유하여 미국, 일본 등의 선진국에서 의류 및 인테리어용으로 채택하여 널리 사용되고 있다. 그러나, polypropylene 섬유는 다른 섬유에 비해 융점이 매우 낮아 내열성이 약하여 가공 공정시 고온을 피해야 하고, 곁가지가 거의 없고 섬유 분자 구조가 매우 조밀하며 탄소와 수소로만 이루어진 분자구조에 의한 극소수성 성질 때문에 다른 종류의 물질들과 접착력이 없어 사용에 제약을 주어 다양한 용도로의 활용이 제한되고 있는 실정이다. 본 연구에서는 Polypropylene 섬유의 제품화에 필요한 요소 기술의 기초를 마련하고자 대기압 플라즈마를 적용하여 소수성 표면을 지니는 표면을 친수화 함으로써 polypropylene 섬유에 후가공이 가능하도록 한다. 따라서 Plasma 표면 처리에 의해 polypropylene 섬유에 미치는 영향에 대하여 조사하고, 표면을 친수화 함으로써 습윤성, 접착성 등 다양한 가공 기술을 적용하여 PP 섬유의 기능성을 향상시키고자 한다. 플라즈마 처리에 의한 폴리프로필렌 섬유의 모폴로지 변화는 주사전자현미경 (FE-SEM)으로 확인하였으며 표면개질 효과는 Wicking Test로 평가하였다.

• Journal of the Korean Electrochemical Society
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• v.20 no.2
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• pp.41-48
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• 2017

Herein, we have fabricated an ultrathin aluminum oxide ($Al_2O_3$) coated PP separator by using a RF sputter deposition process. Approximately 20 nm thickness coating layer on the bare PP separator was formed at the power of 55 W for 2 minutes without thermal damage. Whereas only permeability of the coated separator was degraded slightly, other properties such as thermal stability, uptake amount of liquid electrolyte, and ionic conductivity were improved comparing to the bare PP separator. As a result, an only 20-nm-thick $Al_2O_3$ coating layer could improve the rate capability compared with a bare PP separator under a high current density.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.16 no.1
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• pp.8-14
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• 2015

Plastics have brought a significant progress in reducing the weight of automotive parts and improving gas emissions by replacing steel parts. The front end module (FEM) carrier, which was made from long glass fiber reinforced polypropylene (PP-LFT), is one of the most successful examples. On the other hand, more research on the fatigue behavior and vibration durability of automotive plastic parts will be needed to improve the long-term reliability. This paper analyzed the durability of the PP-LFT, which is fundamental to fatigue design and analysis of FEM carrier. Various fatigue tests were conducted at different stress ratios to evaluate the relationship between the fatigue life and stress amplitude or mean stress level. In the case of a fixed stress amplitude, the change in fatigue life with the stress ratio was 2~6% larger than the case of fixed maximum stress. Furthermore, this study observed the mechanism of initiation and propagation of the fatigue cracks in PP-LFT by scanning electron microscopy.

• 한국신재생에너지학회:학술대회논문집
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• 2011.11a
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• pp.176.1-176.1
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• 2011

세계적으로 석유 기반 자원의 고갈에 따른 부족, 기후변화협약 및 환경규제 강화에 의해 세계적으로 바이오소재를 이용하고자 하는 연구와 더불어 유리강화복합재료의 대체물질로 적합한 천연섬유를 보강재로 사용하는 바이오복합재료의 연구 또한 활발하게 진행되고 있다. 최근 새로운 신재생에너지원으로 각광 받고 있는 바이오에너지 중 해조류는 가장 자연친화적이고 생산력이 뛰어난 바이오매스로 알려져 있다. 해조류는 바닷물 속에 녹아 있는 탄소를 흡수할 뿐만 아니라 광합성을 통해서도 탄소를 흡수하면서 성장하기 때문에 탄소흡수원의 역할을 하게 되며, 해조류 바이오에너지를 생산할 경우 화석연료를 대체하여 지구온난화의 주범인 온실가스를 감축하는 기능을 한다. 본 연구에서는 해조류를 이용한 바이오에너지 생산 공정에서 2차적으로 발생하는 부산물을 보강재로 사용한 바이오복합재료의 제조와 제조된 바이오복합재료의 열적 특성 및 동역학적 특성을 분석하였다. 해조류 부산물의 화학적 전처리에 따른 Thermogravimetric analysis(TGA) 분석 결과로 cellulose 함량이 가장 높고 불순물이 적은 황산 처리한 파래를 이용해 파래/Polypropylene(PP) 바이오복합재료를 다양한 보강비율 (20-50wt%)로 압축성형 하였다. 파래/PP 바이오복합재료의 저장탄성률은 파래 함량이 40wt%일 때 4.0 Gpa으로 최대값을 보였으며 이는 PP 매트릭스와 비교했을 때 약 8.1% 향상된 결과이다. 파래/PP 바이오보합재료의 열팽창 특성은 파래 함량이 증가함에 따라 열팽창계수가 낮아지는 경향으로 50wt%일 때 가장 낮은 값을 나타내었으며 이는 PP 매트릭스와 비교했을 때 약 56% 향상된 결과이다. 따라서 비생분해성 고분자에 새로운 신재생 바이오매스인 해조류를 보강재로 사용하여 열적 특성 및 동역학적 특성이 향상된 친환경적인 바이오복합재료의 제조 가능성을 확인하였다.

• Journal of Adhesion and Interface
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• v.8 no.3
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• pp.9-15
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• 2007

The interfacial evaluation of surface modified Jute fiber/polypropylene (PP) composites before and after hydration was investigated using micromechanical test and dynamic contact angle measurement. The IFSS of alkaline and silane-treated Jute fiber/PP composites increased, whereas after hydration, the IFSS of the untreated, alkaline- and silane-treated Jute fibers/PP composites decreased due to swelled fibrils by water infiltration. The interfacial adhesion of silane treated fiber/PP composites was higher than alkaline-treated or the untreated cases. The surface energies of Jute fiber treated under various conditions were obtained using dynamic contact angle measurement. Especially after hydration, the thermodynamic work of adhesion was calculated by considering water interlayer, which indicated the stability of IFSS between silane treated Jute fiber and PP matrix showing better than others.

• Polymer(Korea)
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• v.36 no.4
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• pp.461-469
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• 2012

The surface modification and characterization of Ar-plasma treated polypropylene (PP) blend are investigated using x-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and contact angle measurement. An increase in Ar-plasma treatment time leads to an increase in wettability, oxygen containing polar functional groups, the amount of talc, and surface roughness on the PP blend surface. A careful observation using SEM indicates that there exists a skin layer consisting of only PP component. The difference in viscosity between PP and rubber particles facilities the formation of skin layer. However, it is found that an increase in Ar-plasma treatment time helps to decrease the thickness of skin layer. Additional methodologies for the elimination of skin layer during injection molding are also discussed. The surface modification and morphological alteration induced by Ar-plasma treatment provides a hydrophilic state, followed by the improvement in wettability, on the PP blend surface.

• Membrane Journal
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• v.11 no.3
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• pp.109-115
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• 2001

Pore-filled ion-exchange membranes in which polypropylene(PP) microporous membrane was used as a nascent membrane were prepared by an in-situ cross-linking technique. Poly(vinylbenzyl chloride)(PVBCI) reacted with piperazine(PIP) or 1,4-diaminobicyclo[2,2,2]octane(DABCO) in a di-methylforamide(DMF) solution was filled in the pores of the microporous base membrane. After gellation the remaining chloromethyl groups were, then reacted with an amine such as trimethylamine to form positively charged, ammonium site. This will produce the pore-filled anion-exchange membrane. It was shown that this simple 2 step procedure gave dimensionally stable, pore-filled membranes in which the MG of polymer gel and degree of cross-linking could be easily controlled by the concentration of PVBCI and cross-linker in the starting DMF solution. Specially, high water permeability (7.8 kg/$m^2$hr, host membrane: PP3, MG: 73%, degree of cross-linking: 10%, crosslinker: PIP) at ultra low pressure(100 kPa) indicates the produced pore-filled membranes is usable as a water softening membrane.

• Elastomers and Composites
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• v.41 no.4
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• pp.245-251
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• 2006

Thermoplastic elastomer was prepared from dynamical vulcanization of isotactic polypropylene(iPP)/nitrile rubber blend (NBR/iPP=70/30 wt/wt) in an internal mixer using dicumyl peroxide (DCP) as a curing agent and zinc dimethacrylate (ZDMA) as a coagent. There was a great improvement in tensile and tear strength, elongation-at-break and lower tension set when ZDMA was incorporated into the blend, which is supposed to be due to the increase in crosslink density or the rubber phase and the reduction in size of the rubber particles. It was revealed that the dynamically vulcanized blend exhibited good reprocessibility, indicating its thermoplastic nature.

• Journal of Korean Society of Environmental Engineers
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• v.28 no.5
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• pp.527-534
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• 2006

The purpose of this study is the development of more effective filter-type polymer adsorbent for removal of anionic pollutants from wastewater. In order to synthesize the polymer adsorbent that possesses anionic exchangeable function, carboxyl(-COOH) group of PP-g-AA nonwoven fabric was converted into amine($-NH_2$) group by the chemical modification using diethylene triamine(DETA). FT-IR data indicate that amine group was introduced into PP-g-AA through amidation of grafted acrylic acid by reaction with DETA. The degree of amination increased with increase in the reaction time and temperature of the chemical modification process, and was significantly improved by the pre-swelling treatment of PP-g-AA with solvent and addition of metal chlorides as a catalyst in following order as $NH_4OH>MeOH{\geq}HCl{\geq}H_2O\;and\;AlCl_3>FeCl_3{\geq}SnCl_2{\gg}ZnCl_2{\geq}FeCl_2$, respectively. However, the addition of catalyst limited the reusability of DETA, hence was less useful from the viewpoint of cost effectiveness and waste management. The anion exchange capacity of the aminated PP-g-AA(PP-g-AA-Am) increased with increase in the degree of amination, but it reached maximum value at the degree of amination as about $50{\sim}60%$. The anion exchange capacity of PP-g-AA-Am was higher than those of commercial anion resins.