탄소나노튜브는 우수한 기계적 특성, 전기적 및 자기적 성질 뿐만 아니라 나노 크기의 직경 및 높은 종횡비를 나타낸다. 이는 고강도 고분자 복합체의 이상적인 보강제로 사용할 수 있다. 기능성이 부과된 탄소나노튜브는 기능성 재료 및 복합재료의 제조와 같은 분야에서 아주 유력한 재료로 믿어진다. 탄소나노튜브-고분자 복합체는 탄소나노튜브의 우수한 기능성과 고분자의 우수한 가공성을 가질 것으로 기대된다. 그러나, 탄소나노튜브는 보통 반 델 바알스 작용에 의한 안정화된 번들을 형성하기 때문에 고분자 기지에 배열이나 분산이 상당히 어렵다. 탄소나노튜브 강화복합체의 제조에서 가장 큰 이슈는 고분자내에 탄소나노튜브의 효과적인 분산이며, 기지내에 탄소나노튜브의 배열과 양의 조절이다. 고분자 기지내에 탄소나노튜브의 분산은 용액혼합, 벌크 혼합, 용융혼합, 즉시 고분자화 반응 및 탄소나노튜브의 화학적 기능화 등과 같은 몇 가지 방법이 있다. 본 논평에서는 이들 방법과 고성능 탄소나노튜브-고분자 복합체의 제조에 대하여 서술하고자 한다.
탄소나노튜브는 우수한 기계적 특성, 전기적 및 자기적 성질 뿐만 아니라 나노 크기의 직경 및 높은 종횡비를 나타낸다. 이는 고강도 고분자 복합체의 이상적인 보강제로 사용할 수 있다. 기능성이 부과된 탄소나노튜브는 기능성 재료 및 복합재료의 제조와 같은 분야에서 아주 유력한 재료로 믿어진다. 탄소나노튜브-고분자 복합체는 탄소나노튜브의 우수한 기능성과 고분자의 우수한 가공성을 가질 것으로 기대된다. 그러나, 탄소나노튜브는 보통 반 델 바알스 작용에 의한 안정화된 번들을 형성하기 때문에 고분자 기지에 배열이나 분산이 상당히 어렵다. 탄소나노튜브 강화복합체의 제조에서 가장 큰 이슈는 고분자내에 탄소나노튜브의 효과적인 분산이며, 기지내에 탄소나노튜브의 배열과 양의 조절이다. 고분자 기지내에 탄소나노튜브의 분산은 용액혼합, 벌크 혼합, 용융혼합, 즉시 고분자화 반응 및 탄소나노튜브의 화학적 기능화 등과 같은 몇 가지 방법이 있다. 본 논평에서는 이들 방법과 고성능 탄소나노튜브-고분자 복합체의 제조에 대하여 서술하고자 한다.
Carbon nanotubes (CNTs) exhibit excellent mechanical, electrical, and magnetic properties as well as nanometer scale diameter and high aspect ratio, which make them an ideal reinforcing agent for high strength polymer composites. The functionalized CNTs are believed to be very promising in the field...
Carbon nanotubes (CNTs) exhibit excellent mechanical, electrical, and magnetic properties as well as nanometer scale diameter and high aspect ratio, which make them an ideal reinforcing agent for high strength polymer composites. The functionalized CNTs are believed to be very promising in the fields such as preparation of functional and composite materials. CNT-Polymer composites are expected to have good processability characteristics of the polymer and excellent functional properties of the CNTs. However, since CNTs usually form stabilized bundles due to Van der Waals interactions, are extremely difficult to disperse and align in a polymer matrix. The biggest issues in the preparation of CNT-reinforced composites reside in efficient dispersion of CNTs into a polymer matrix, and the alignment and control of the CNTs in the matrix. There are several methods for the dispersion of nanotubes in the polymer matrix such as solution mixing, bulk mixing, melt mixing, in-situ polymerization and chemical functionalization of the carbon nanotubes, etc. These methods and preparation of high performance CNT-polymer composites are described in this review.
Carbon nanotubes (CNTs) exhibit excellent mechanical, electrical, and magnetic properties as well as nanometer scale diameter and high aspect ratio, which make them an ideal reinforcing agent for high strength polymer composites. The functionalized CNTs are believed to be very promising in the fields such as preparation of functional and composite materials. CNT-Polymer composites are expected to have good processability characteristics of the polymer and excellent functional properties of the CNTs. However, since CNTs usually form stabilized bundles due to Van der Waals interactions, are extremely difficult to disperse and align in a polymer matrix. The biggest issues in the preparation of CNT-reinforced composites reside in efficient dispersion of CNTs into a polymer matrix, and the alignment and control of the CNTs in the matrix. There are several methods for the dispersion of nanotubes in the polymer matrix such as solution mixing, bulk mixing, melt mixing, in-situ polymerization and chemical functionalization of the carbon nanotubes, etc. These methods and preparation of high performance CNT-polymer composites are described in this review.
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제안 방법
39 synthesized MWNT-reinforced polyimide nanocomposites by in-situ polymerization of monomers in the presence of acylated MWNTs, as shown in Scheme 1. In this work, MWNTs were functionalized with acyl groups, and then reacted with biphenyltetracarboxylic dianhydride to form MWNT-poly(amic acid). The final MWNT-polyimide nanocomposite films were obtained by imidization of MWNT-poly-(amic acid) at 350 ℃ for 1 h under vacuum.
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