• Tribology and Lubricants
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• v.39 no.3
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• pp.111-117
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• 2023

This paper presents an experimental investigation of the tribological characteristics of PTFE composites filled with nano CuO particles under low sliding speed and load. All the specimens were prepared by sintering. Before sintering, the mixture of PTFE powder and CuO particles were mixed by a high-speed mixer using CuO volume fractions of 0.2 vol. % and 5 vol. %. Each mixture was sintered at 350 ℃ for 30 min on the steel disk. We conducted ball-on-disk sliding test an hour using a steel ball against PTFE composites, including pure PTFE. The load and sliding speed used was 2 N and 0.01 m/s, respectively. Adding nano CuO particles increases the friction coefficient because of the abrasiveness of hard nano CuO particles. The highest coefficient of frictions was obtained from 5 vol. % CuO. Conversely, the lowest wear of the composites was obtained from the 5 vol. % CuO nanocomposite. This study reveals that the addition of nano CuO particles can lower the wear of PTFE, despite an increase in the coefficient of friction. However, the coefficient friction is still moderate compared to other engineering polymers. In addition, the amount of CuO nano particles has to be optimized to reduce friction and wear at the same time.

• Journal of Adhesion and Interface
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• v.22 no.3
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• pp.106-110
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• 2021

Recently, research using waste among eco-friendly materials has been attracting attention. In this study, we investigated the physical properties of blends in which high density polyethylene (HDPE) was filled with waste gypsum (CaSO₄) generated during fertilizer manufacturing. Composites were prepared by adding the gypsum content 0~20 wt% using a twin screw extruder. The mechanical, rheological, and thermal properties of the composites were evaluated. It was found that the tensile strength of the composites was less than 4.1% compared to that of unfilled HDPE, so there is no significant deterioration in physical properties. The thermal stability of the composites was improved as the gypsum content increased and the gypsum content had little effect on the viscosities of the composites.

• Composites Research
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• v.30 no.5
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• pp.316-322
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• 2017

Carbon fiber is a material with excellent mechanical, electrical and thermal properties, which is widely used as a composite material made of a polymer matrix. However, this composite material has a weak point of interlaminar delamination due to weak interfacial bond with polymer matrix compared with high strength and elasticity of carbon fiber. In order to solve this problem, it is essential to use reinforcements. Due to excellent mechanical properties, graphene have been expected to have large improvement in physical properties as a reinforcing material. However, the aggregation of graphene and the weak interfacial bonding have resulted in failure to properly implement reinforcement effect. In order to solve this problems, dispersibility will be improved. In this study, functionalization of graphene nanoplatelet was proceeded with melamine and mixed with epoxy polymer matrix. The carbon fiber reinforced polymer composites were fabricated using the prepared graphene nanoplatelet/epoxy and flexural properties and interlaminar shear strength were measured. As a result, it was confirmed that the dispersibility of graphene nanoplatelet was improved and the mechanical properties of the composite material were increased.

• Composites Research
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• v.36 no.2
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• pp.126-131
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• 2023

Growing environmental concerns regarding pollution caused by conventional plastics have increased interest in biodegradable polymers as alternative materials. The purpose of this study is to develop a 100% biodegradable nanocomposite material by introducing organic nucleating agents into the biodegradable and thermoplastic resin, poly(lactic acid), to improve its properties. Accordingly, cellulose nanofibers, an eco-friendly material, were adopted as a substitute for inorganic nucleating agents. To achieve a uniform dispersion of cellulose nanofibers (CNFs) within PLA, the aqueous solution of nanofibers was lyophilized to maintain their fibrous shape. Then, they were subjected to primary mixing using a twin-screw extruder. Test specimens with double mixing were then produced by injection molding. Differential scanning calorimetry was employed to confirm the reinforced physical properties, and it was found that the addition of 1 wt% CNFs acted as a reinforcing material and nucleating agent, reducing the cold crystallization temperature by approximately 14℃ and increasing the degree of crystallization. This study provides an environmentally friendly alternative for developing plastic materials with enhanced properties, which can contribute to a sustainable future without consuming inorganic nucleating agents. It serves as a basis for developing 100% biodegradable green nanocomposites.

• Journal of the Microelectronics and Packaging Society
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• v.25 no.4
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• pp.35-40
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• 2018

Simple and useful synthetic process to control the morphology of block copolymers (BCPs) is required for implementation in various device applications. However, the conventional method to use colloidal templates is not enough to realize the production of pure and massive core-shell nanoparticles due to the cost-intensive complex process. Here, we introduce a novel and facile synthesis method to realize the formation of core-shell $SiO_x$ nanoparticle power by employing an immersion annealing of a sphere-forming poly(styrene-b-dimethylsiloxane) (PS-b-PDMS) BCP. We successfully obtained a PS-encapsulated $SiO_x$ nanoparticle with a diameter of ~20 nm. In addition, we analyzed how the mixing ratio of heptane/ethanol affects the BCP morphology of self-assembled PS-b-PDMS nanoparticles, showing a worm-like structure under the optimum immersion conditions. This useful approach is expected to be extendable to other solvent-based BCP synthesis, providing a new guideline for unique BCP production.

• Membrane Journal
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• v.27 no.2
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• pp.154-166
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• 2017

Polymeric films for gas barrier applications such as food packaging and electronic devices have attracted great interest due to their cheap, light and easy processability among gas barrier materials. Especially in electronic devices, extremely low gas permeance is necessary for maintaining the device performance. However, current polymeric barrier films still suffer from relatively high gas permeance than other materials. Therefore, there have been strong needs to enhance the gas barrier performance of polymeric barrier films while keep their own advantages. Recently, graphene is highlighted as a 2D-layered material for gas barrier applications. However, owing to the poor workability and difficulty to produce in engineering scale, graphene oxide (GO) is on the rise. GO consists of oxygen-containing functional groups on surface with intrinsic 2D-layered structure and high aspect ratio, and it can be well-dispersed in aqueous polar solvents like water, resulting in scalable mass production. Here, we prepared GO incorporated polyimide (PI) nanocomposites. PI is widely used barrier polymer with high mechanical strength and thermal and chemical stability. We demonstrated that PI/GO nanocomposites could perform as a gas barrier. Furthermore, surfactants (Triton X-100 (TX) and Sodium deoxycholate (SDC)) are introduced to enhance the gas barrier performance by improving the degree of dispersion of GO in PI matrix. As a result, TX enhanced the gas barrier performance of PI/GO nanocomposites which is similar to predicted value. This finding will provide new insight to polymer nanocomposites for gas barrier applications.

• Proceedings of the Korean Fiber Society Conference
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• 2002.04a
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• pp.321-324
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• 2002

Recently, organic-inorganic nanocomposites have attracted great interest from researchers since they frequently exhibit unexpected hybrid properties synergistically derived from two components[1]. The addition of highly dispersed inorganic nano-sized fillers permits improvement of certain properties of polymers as compared with conventional particulate composites; increase of modulus and strength, improved barrier properties, increase in solvent and heat resistance, and good optical properties[2]. (omitted)

• Proceedings of the Korean Vacuum Society Conference
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• 2010.08a
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• pp.217-217
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• 2010

유기물/무기물 나노 복합재료는 고온과 저전력에서 동작해야하는 차세대 전자 소자와 광소자 제작에 대단히 유용한 소재이다. 간단하고 저렴한 제조 방법과 휘어짐이 가능한 특성을 이용하여 유기물/무기물 나노 복합재료를 사용한 비휘발성 메모리 소자의 제작과 메모리 특성에 대한 연구가 수행되었으나, SnO2 나노 입자가 삽입된 고분자 박막을 기반으로 제작한 저항 구조의 비휘발성 메모리 소자인 유기 쌍안정성 소자에 대한 연구는 상대적으로 미흡하다. 본 연구에서는 poly(methyl methacrylate) (PMMA) 박막 안에 분산된 SnO2 나노 입자를 사용하여 제작한 유기 쌍안정성 소자의 메모리 특성을 관찰하였다. 소자를 제작하기 위해 나노 입자의 전구체인 Tin 2-ethylhexanoate을 dibutyl ether에 용해시킨 후, 화학적 방법을 사용하여 용매 안에서 SnO2 나노 입자를 합성하였다. 합성한 SnO2 나노 입자와 PMMA를 클로로벤젠에 용해하여 고분자 용액을 제작하였다. 전극인 indium-tin-oxide가 증착된 유리 기판 위에 제작한 고분자 용액을 스핀 코팅하고, 열을 가해 용매를 제거하여 SnO2 나노 입자가 분산되어 있는 PMMA 나노복합체를 형성하였다. 그 위에 Al 전극을 증착하여 유기 쌍안정성 소자를 완성하였다. 제작된 소자에 전압을 인가하여 전류를 측정한 결과 유기 쌍안정성 소자에서는 동일 전압에서 높은 전류 (ON 상태)와 낮은 전류 (OFF 상태)가 흐르는 쌍안정성 특성을 나타냈다. 그러나 SnO2 나노 입자가 없는 PMMA 박막으로 형성된 소자에서는 전류-전압 측정에서 쌍안정성 특성이 나타나지 않았다. 따라서 PMMA 박막 안에 삽입된 SnO2 나노 입자가 유기 쌍안정성 소자의 메모리 효과를 나타내는 원인임을 알 수 있었다. 전류-시간 측정 결과는 소자의 ON 상태 및 OFF 상태 전류가 시간에 따른 큰 변화 없이 1000 사이클 이상 지속적으로 유지 하고 있음을 보여 줌으로써 유기 쌍안정성 소자를 장시간 사용할 수 있음을 확인시켜 주었다.

• Prospectives of Industrial Chemistry
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• v.24 no.6
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• pp.3-18
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• 2021

가역적인 표면 젖음성의 제어가 가능한 스마트 표면은 첨단 센서, 기능성 멤브레인 등 여러 산업분야에 적용될 수 있는 계면제어 기술로써 많은 관심을 받을 것으로 기대된다. 표면의 젖음성은 표면의 화학적 구조와 기하학적 입체 구조에 의해 영향을 받는 데, 특히 외부자극에 의해 소재 물성을 가변시킬 수 있는 스마트 고분자 소재를 나노구조가 제어된 표면에 도입함으로써 표면의 젖음성을 초발수에서 초친수로 가역적으로 전환시킬 수 있는 스마트 표면을 효과적으로 구현할 수 있다. 자극 응답성 스마트 소재는 인가하는 외부자극에 따라 물리적 자극(빛, 온도, 전기, 자기)과 화학적 자극(pH, 용매, 이온)으로 구분할 수 있으며, 이를 복합적으로 적용한 이중/다중 유발 자극에 반응하는 소재가 있다. 본 기고문에서는 외부자극에 응답하는 자극응답성 고분자를 나노 구조 표면에 도입하여 초발수에서 초친수로의 가역적인 젖음성 변화가 가능한 고기능성 스마트 표면의 최근 연구 동향과 미래 전망에 대해 소개하고자 한다. 이런 다양한 외부자극을 이용한 표면 특성의 가역적 제어 기술을 통해 물-오일의 분리, 바이오센서, 약물 전달, 소프트로보틱스와 같은 스마트 소재의 잠재적 발전 가능성 또한 엿볼 수 있을 것으로 기대된다.

• Applied Chemistry for Engineering
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• v.24 no.6
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• pp.621-627
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• 2013

In order to apply eco-friendly poly(propylene carbonate) (PPC) into barrier packaging materials, six different PPC/exfoliated graphite (EFG) nanocomposite films with different EFG were successfully prepared by a solution blending method. Their water sorption behavior was gravimetrically investigated as a function of the EFG content and interpreted with respect to their chemical structure and morphology. The water sorption isotherms were reasonably well fitted by Fickian diffusion model, regardless of morphological heterogeneities. With increasing the EFG content, the diffusion coefficient and water uptake decreased from $12.5{\times}10^{-10}cm^2sec^{-1}$ to $7.2{\times}10^{-10}cm^2sec^{-1}$ and from 8.9 wt% to 4.2 wt%, respectively, which indicates that the moisture resistance capacity of PPC was greatly enhanced by incorporating EFG into PPC. The enhanced water barrier property of the PPC/EFG nanocomposite films with the high aspect ratio EFG makes them potential candidates for versatile packaging applications. However, to maximize the performance of the nanocomposite films, further researches are required to increase the compatibility of EFG in the PPC matrix.