高性能聚合物/碳纳米管复合薄膜的制备与研究
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摘要
本论文采用碳纳米管作为改性剂,对高性能聚合物进行改性,得到了抗静电用高性能聚合物/碳纳米管复合薄膜,期望能在航空航天等领域得到应用。
     第一章介绍了碳纳米管的结构、制备、纯化方法,综述了聚合物/碳纳米管复合薄膜的制备方法,以及聚合物/碳纳米管的力学、电学和其他功能增强的研究。
     第二章通过控制碳纳米管在聚芳醚腈基体中的分布,实现了碳纳米管在聚合物基体中的梯度分布,制备得到了聚芳醚腈/碳纳米管复合梯度薄膜,使复合薄膜一侧保持其电绝缘性,另一侧为半导体,从而得到了一侧抗静电的聚芳醚腈/碳纳米管复合梯度薄膜。
     第三章通过对改性剂碳纳米管进行表面酸化处理,得到了表面含有羧基的碳纳米管,进一步酰氯化,从而得到表面含有酰氯基团的碳纳米管,并且通过与氨基酸接枝,能实现碳纳米管的水分散性。
     第四章通过原位聚合的方法将酰氯化碳纳米管接枝到聚芳醚酮分子链上,制备得到了聚芳醚酮/碳纳米管复合薄膜。碳纳米管的加入使得聚芳醚酮薄膜的力学性能大大提高,从而得到了力学性能增强的聚芳醚酮/碳纳米管复合薄膜,同时其电阻率大大降低,但是并没有达到抗静电的数量级。同样,通过原位聚合的方法将酰氯化碳纳米管接枝到聚酰亚胺分子链上,制备得到了聚酰亚胺/碳纳米管复合薄膜,在保持聚酰亚胺薄膜透明性的同时,使得聚酰亚胺薄膜的电阻率大大降低,达到了抗静电的要求。同时铜离子的加入,使得薄膜的电阻率进一步降低,最低达到了107数量级。这种材料不但具有透明性,而且达到了抗静电的数量级,在航空航天等领域具有广泛的应用前景。
Since the first observation of high performance polymers in USA at the end of 50’s, extensive research in this subject has been aroused. As most important part of polymer materials, high performance polymers have been widely used in the fields such as aerospace, electronics, micro electronics, fine mechanic tools, nuclear industry, as well as separation membranes, liquid crystal display, and Langmuir-blodgett films, owing to their excellent thermal stability. As the development of the technology of synthesis and process, the application of high performance polymers have been enlarged into wider areas, such as automobile, electronic appliance, office products, and or so.
     As the rapid development of aerospace technology all over the world, all kinds of high performance polymer films have been widely used. Several space mission concepts proposed by NASA are based on the use large, deployable, and ultra-lightweight vehicles (e.g. Gossamer spacecraft) consisting of both structural and polymer film components.
     However, future Gossamer spacecraft will require films that are durable to the space environment and compliant. Compliance is needed so that the film can be folded into caompact volumes found on conventional launch vehicles. Once in orbit, the folded film is deployed to create structures, that are many square meters in size. To be space durable, the film must exhibit resistance to many environment factors, such as atomic oxygen (AO) in low earth orbit, UV and vacuum UV radiation, and electron and proton attack. Therefore, high performance films are needed to meet these requirements.
     However, as far as the application of high performance polymers are concerned, the static electricity is becoming a big problem. Generally speaking, high performance polymers are kinds of insulating materials. Therefore, electric charge accumulation can easily take place at the surface of the polymers, as a result, the static electricity can be formed, which may bring many hazards.
     As the electric charge accumulation takes place, the surfaces of high performance polymers can absorb dust easily and will be very dangerous while touching. Meanwhile, the material can then behave like a capacitor and discharge in a single event causing considerable damage to surrounding materials and electronics on the vehicles.
     Therefore, it’s becoming vital to prepare anti-static high performance polymer films, which can be widely used for the following filds: (1)packaging materials; (2)for solar cell usage. It require that the films for both applications exhibit low solar absorptivity (α)and high thermal emissivity (ε), i.e., the film has anti-static properties while maintaining its own transparency.
     The most effective method for charge mitigation is to endow the insulating materials conductive properties. As we know, the charge can mitigate easily on the conductive surface. As far as the anti-static high performance polymers are concerned, it’s necessary to modify the high performance polymers, while maintaining the excellent mechanical and thermal properties of high performance polymers.
     The current state-of-the-art to impart electrical conductivity while maintaining a lowαand high optical transparency has been through the use of conductive coatings such as indium-tin oxide (ITO). While exhibiting high surface conductivity, these coatings are rather brittle and make handling difficult. Once the coating is broken (cracked) by handling or on orbit, the conductive pathway is lost.
     Since the discovery of nano materials, the research focued on the polymer/nano materials nanocomposite have been aroused much attention. Especially carbon nanotubes, since their discovery in 1991, they have captured the attention of researchers worldwide. Understanding their unique properties and exploring their potential application have been a main driving force for this area.
     In terms of mechanical properties, nanotubes are among the strongest and most resilent materials known to exist in nature. A nanotube has Young’s modulus of 1.8 TPa and a tensile strength about a hundred times higher than steel and can tolerate large strains before mechanical failure. Therefore, Nanotubes can be used as an excellent candidate for enhancement application in the fields such as aerospace, automobile, ship, sport products, etc.
     Extensive studies have been shown that a nanotube can behave as a well-defined metallic, semi-conducting or semi-metallic wire depending on its chirality and diameter. Therefore, they can be used as anti-static materials effectively.
     The aim for this thesis is to modify the high performance polymers by carbon nanotubes and to obtain anti-static high performance polymers/carbon nanotubes nanocomposite films, which may have potential applications in aerospace application.
     Generally, the introduction of carbon nanotubes into polyarylene ether nitrile has little effect on the mechanical properties of polymer matrix. Therefore, in our work, carbon nanotubes embedded in a polymer film with a gradient distribution were successfully obtained. For composite films with gradient distributions of carbon nanotubes, the upper surface behaves as an intrinsic insulator, while the lower one behaves as a semiconductor, or even as a conductor. It is also found that with an increase of 1 wt% carbon nanotubes, the resistance of the bottom surface decreases by 2-3 orders of magnitude, as compared with pure polyarylene ether nitrile; furthermore, when the proportion of carbon nanotubes increased up to 5 wt%, the resistance of the bottom surface shows only very little changes. As a result, sufficient matrix conductivity of the bottom surface could be achieved at a lower filler concentration with carbon nanotubes in a gradient distribution. Meanwhile, the thermal stability, glass transition termperature and tensile properties of the matrix are maintained. There is considerable interest in such gradient composite films, which could be applied in the electrical engineering, electronics and aerospace fields, for their excellent mechanical properties, thermal stability and novel electrical properties.
     In order to obtain efficient dispersion of carbon nanotubes in polymer matrix, it’s necessary to modify carbon nanotubes. At first, we purified carbon nanotubes by ultrasoncating them in the strong acids (H2SO4/HNO3, 3:1). There were many carbonyl acid groups attached on the carbon nanotubes after acid treatment, which had been proved by FTIR. At the same time, the content of carbonyl acid groups had be quantitatively determined by the titration. The purified carbon nanotubes could be acylated easily while refluxing in SOCl2. All of carbonyl acid groups on the surface and at the end of carbon nanotubes attended the reaction and changed to acyl chloride groups after refluxing for 24 hours. The acyl chloride groups played important roles in the chemistry of carbon nanotubes, since they could react with hydroxyl groups and amine groups easily. Therefore, we tried to react these acylated carbon nanotubes with lysine, and to obtain water dispersible lysine modified carbon nanotubes.
     As the development of multi-functional materials in the fields such as aerospace, electronic packaging materials, the optical transparent anti-static polymer films are becoming more and more important. Therefore, it’s meaningful to develop anti-static films with optical transparency in our work.
     Therefore, multi-walled carbon nanotubes (MWNTs) modified PAEK nanocomposites were synthesized by in situ polymerization of monomers of interest in the presence of pre-treated MWNTs here. This process enabled uniform dispersion of MWNT bundles in the polymer matrix. The resultant MWNTs-PAEK nanocomposite films were optically transparent with significant mechanical enhancement at a very low loading (0.5 wt %). These MWNT-polymer nanocomposites are potentially useful in a variety of aerospace and terrestrial applications, due to their combination of excellent properties of MWNTs with PAEK. However, the resistance of the nanocomposite films didn’t reach the anti-static orders.
     It’s becoming urgent to develop this kind of materials. We tried another polymer matrix, polyimide. A process to efficiently disperse MWNT bundles in polyimide is carried out in this work. This process involves in situ polymerization of the monomers of interest in the presence of acylated MWNTs during the polymerization process. The acyl groups associated with the MWNTs attended the reaction through forming amide bonds. The goal of our work was to develop a method to completely disperse MWNT bundles into a given high perfomance polymer matrix on nanoscale level to produce a mechanically reinforced and optically transparent nanocomposite film with anti-static property. And the results showed that the obtained MWNTs-polyimide nanocomposite films were optically transparent with significant mechanical enhancement at a very low loading (0.5 wt %). Furthermore, the introduction of carbon nanotubes had decreased the resistance of composite films largely, and the obtained composite films exhibited anti-static property, which can satisfy the requirement of optical transparent anti-static films application. Meanwhile, the resistivity of the composite films can be further lowered by introduction a little amount of Cu ions.
引文
[1] IIJIMA S. Helical microtubules of graphitic carbon [J]. Nature, 1991, 354: 56-58.
    [2] LIU K, SUN YH, CHEN L, et al. Controlled growth of super-aligned carbon nanotube arrays for spinning continuous unidirectional sheets with tunable physical properties [J]. Nano Letters 2008; 8:700-705.
    [3] ONCEL C, YURUM Y. Carbon nanotube synthesis via the catalytic CVD method: A review on the effect of reaction parameters [J]. Fullerenes Nanotubes and Carbon Nanostructures 2006, 14(1):17-37.
    [4] SHIN Y S, YANG J H, PARK C Y, et al. Synthesis of crystalline carbon nanotube arrays on anodic aluminum oxide using catalyst reduction with low pressure thermal chemical vapor deposition [J]. Japanese Journal of Applied Physics Part 1-Regular Papers Brief Communications & Review Papers 2006, 45(3A):1869-1872.
    [5] TURANO S P, READY J. Chemical vapor deposition synthesis of self-aligned carbon nanotube arrays [J]. Journal of Electronic Materials 2006, 35:192-194.
    [6] MALHOTRA S V. Synthesis of carbon nanotube gels with Ionic liquids [J]. Abstracts of Papers of the American Chemical Society 2005, 230: U2208-U09.
    [7] CHUANG C C, LIU W L, CHEN W J, et al. The role of Ti interlayer in carbon nanotube growth [J]. Surface & Coatings Technology 2008, 202: 2121-2125.
    [8] CHEN J, MINETT A I, LIU Y, et al. Direct growth of flexible carbon nanotube electrodes [J]. Advanced Materials 2008, 20 (3):566-570.
    [9] PAL S K, TALAPATRA S, KAR S, et al. Time and temperature dependence of multi-walled carbon nanotube growth on Inconel 600 [J]. Nanotechnology 2008, 19 (4):45610-45615.
    [10] YANG Z, CHEN X H, NIE H G, et al. Direct synthesis of ultralong carbon nanotube bundles by spray pyrolysis and investigation of growth mechanism [J]. Nanotechnology 2008, 19:85606-85614.
    [11] ECEIZA A, MARTIN M D, DE LA CABA K, et al. Thermoplastic polyurethane elastomers based on polycarbonate diols with different soft segment molecular weight and chemical structure: Mechanical and thermal properties [J]. Polymer Engineering and Science 2008, 48:297-306.
    [12] WU J, HUANG Q W, MA Y F, et al. Distortion of carbon nanotube array and its influence on carbon nanotube growth and termination [J]. Colloids andSurfaces a-Physicochemical and Engineering Aspects 2008,313:13-17.
    [13]张立德,牟季美.纳米材料和纳米结构[M].北京:科学出版社,2001.
    [14] JIANG Y, WU Y, QIANG Y T, et al. A Catalytic-Assembly Solvothermal Route to Multiwall Carbon Nanotubes at a Moderate Temperature [J]. Journal of the American Chemical Society, 2000,122:12383-12384.
    [15] VANDER WAL R L, TICIH T M. Flame Synthesis of Single-Walled Carbon Nanotubes and Nanofibers [J]. The Journal of Physics Chemistry Part B,2001, 105:10249-10256.
    [16] OLOUGHLIN J L, KIANG C H, WALLACE C H, et al. Rapid Synthesis of Carbon Nanotubes by Solid-State Metathesis Reactions [J]. The Journal of Physics Chemistry Part B, 2001,105:1921-1924.
    [17] MOTIEIM, HACOHENY R, CALDERON MORENO J, et al. Preparing carbon nanotubes and nested fullerenes from supercritical CO2 by a chemical reaction [J]. Journal of the American Chemical Society, 2001,123,8624-8265.
    [18] AGO H, OHSHIMA S, UCHIDA K, et al. Gas-phase synthesis of single-wall carbon nanotubes from colloidal solution of metal nanoparticles [J]. The Journal Physic Chemistry Part B, 2001,105:10453-10456.
    [19] LI W Z, WEN J G, REN Z F. Straight carbon nanotube Y junctions [J]. Applied Physics Letter, 2001,79: 1879-1881.
    [20] AHLSKOG M, SEYNAEVE E, VULLERS R J M, et al. Ring formations from catalytically synthesized carbon nanotubes [J]. Chemical Physics Letters, 1999,300:202-206.
    [21] LIU S, BOESHORE S, FERNANDEZ A, et al. Study of Cobalt-Filled Carbon Nanoflasks [J]. The Journal of Physical Chemistry B, 2001, 105: 7606-7611.
    [22]HIURA H, EBBESEN T W, TANIGAKI K. Opening and purification of Carbon nanotubes in high yields [J]. Advanced Materials, 1995, 7: 275-276.
    [23]RINZLER A G, LIU J, DAI H, et al. Large-scale purification of single-wall carbon nanotubes: process, product, and characterization [J]. Applied Physics A (Material Science & Processing), 1998, 67: 23-27.
    [24]SEKAR C, SUBRAMANIAN C. Purification and characterization of buckminsterfullene, nanotubes and their by-products [J]. Vacuum, 1997, 47: 1289-1292.
    [25]IVANOV V, FONSECA A, NAGY J B, et al. Catalytic production and purification of nanotubes having fullerene-scale diameter [J]. Carbon, 1995, 33: 1727-1738.
    [26] BONARD J M, STORN T, SALVETAT J P, et al. Purification and size-selectionof carbon nanotube [J]. Advanced Materials, 1997, 9: 827-831
    [27]YAMAMOTO K, AKITA S, NAKAYAMA Y. Orientation of carbon Nanotubes using electrophoresis [J]. Japanese Journal of Applied Physics, Part 2 [Letters], 1996, 35 (7B): L917-918.
    [28]BONARD J M, STORN T, SALVETAT J P, et al. Purification and size-selection of carbon nanotubes [J]. Advanced Materials, 1997, 9: 827-831.
    [29]BANDOW S, RAO A M, WILLIAMS K A, et al. Purification of single-wall carbon Nanotubes by microfiltration [J]. Chemical Physics Letters, 1998, 282: 429-434.
    [30]SHELIMOV K B, ESENALIEV R O, RINZLER A G, et al. Purification of single-wall carbon nanotubes by ultrasonically assisted filtration [J]. Chemical Physics Letters, 1998, 282: 429-434.
    [31]DUESBERG B H, XIE S S, ZHOU W Y, et al. Loosely-entangled carbon Nanotubes prepared in modified arc-discharge [J]. Applied Physics A, 1998, 67: 117-119.
    [32]杨占红,李新海,志国等.碳纳米管的纯化[J].化工新型材料,1999, 27: 22-24
    [33]吴崇浩,王世敏,纳米微粒表面修饰的研究进展[J].化工新型材料,2002, 30: 1-5.
    [34]JIN L, BOWER C, ZHOU O, et al. Alignment of carbon Nanotubes in a polymer matrix by mechanical stretching [J]. Applied Physics Letters, 1998, 73: 1197-1199.
    [35]SHAFFER M S P, WINDLE A H. Fabrication and characterization of carbon nanotube/poly (vinyl alcohol) composites [J]. Advanced Materials, 1999, 11: 937-941.
    [36]QIAN D, DICKEY E C, ANDREWS R, et al. Load transfer and deformation mechanisms in carbon nanotube-polystyrene composites [J]. Applied Physics Letters, 2000, 76: 2868-2870.
    [37]DUFRESNE A, PAILLET M, PUTAUX J L, et al. Processing and characterization of carbon nanotube/poly (styrene-co-butyl acrylate) nanocomposites [J]. Journal of Material Science, 2002, 37: 3915-3923.
    [38]PROBST O, MOORE E M, RESASCO D E, et al. Nucleation of polyvinyl alcohol crystallization by single-walled carbon nanotubes [J]. Polymer, 2004, 45: 4437-4443.
    [39]DALMAS F, CHAZEAU L, GAUTHIER C, et al. Multiwalled carbon nanotube/polymer nanocomposites: processing and properties [J]. Journal of Polymer Science, Part B: Polymer Physics. 2005, 43: 1186-1197.
    [40]COLEMAN J N, CADEK M, BLAKE R, et al. High performance nanotube-reinforced plastics: understanding the mechanism of strength increase [J]. Advanced Functional Materials, 2004, 14: 791-798.
    [41]CADEK M, COLEMAN J N, RYAN K P, et al. Reinforcement of polymers with carbon nanotubes: the role of nanotube surface area [J]. Nano Letters, 2004, 4: 353-356.
    [42]ANDREWS R, JACQUES D, MINOT M, et al.Fabrication of carbon multiwall nanotube/polymer composites by shear mixing [J]. Macromolecular Materials and Engineering, 2002, 287: 395-403.
    [43]BREUER O, SUNDARARAJ U. Big returns from small fibers: a review of polymer/carbon nanotube composites [J]. Polymer Composites, 2004, 25: 630-645.
    [44]POTSCHKE P, BHATTACHARYYA A R, JANKE A, et al. Melt mixing of polycarbonate/multi-wall carbon nanotube composites [J]. Compos Interface, 2003, 10: 389-404.
    [45]JIN Z, PRAMODA K, XU G, et al. Dynamic mechanical behavior of melt-processed multi-walled carbon nanotube/poly (methyl methacrylate) composites [J]. Chemical Physics Letters, 2001, 337: 43-47.
    [46]ANDREWS R, JACQUES D, QIAN D L, et al. Multiwall carbon Nanotubes: synthesis and application [J]. Accoustic Chemical Research, 2002, 35: 1008-1017.
    [47]MEMCKE O, KAEMPFER D, WEICKMANN H, et al. Mechanical properties and electrical conductivity of carbon-nanotube filled polyamide-6 and its blends with acrylonitrile/butadiene/styrene [J]. Polymer, 2004, 45: 739-748.
    [48]THOSTENSON E T, CHOU T W. Aligned multi-walled carbon nanotube reinforced composites: processing and mechanical characterization [J]. Journal of Physics D: Applied Physics, 2002, L77-80.
    [49]HAGGENMUELLER R, GOMMANS H H, RINZLER A G, et al. Aligned single-wall carbon Nanotubes in composites by melt processing methods [J]. Chemical Physics Letters, 2000, 330: 219-225.
    [50]AJAYAN P M, SCHADLER L S, GIANNARIS C, et al. Single-walled carbon nanotube-polymer composites: strength and weakness [J]. Advanced Materials, 2000, 12: 750-753.
    [51]LI Q Q, ZAISER M, KOUTSOS V. Carbon nanotube/epoxy resin composites using a block copolymer as a dispersing agent [J]. Physica Status Solidi A-AppliedResearch, 2004, 201: R89-91.
    [52]LAU K T, LU M, CHUN K L, et al. Thermal and mechanical properties of single-walled carbon nanotube bundle-reinforced epoxy nanocomposites: the role of solvent for nanotube dispersion [J]. Composite Science and Technology, 2005, 65: 719-725.
    [53]XU X, THWE M M, SHEARWOOD C, et al. Mechanical properties and interfacial characteristics of carbon-nanotube-reinforced epoxy thin films [J]. Applied Physics Letters, 2002, 81: 2833-2835.
    [54]JIA Z, WANG Z, XU C, et al. Study on poly (methyl methacrylate)/carbon nanotube composites [J]. Material Science and Engineering: A, 1999, 271, 395-400.
    [55]VELASCO-SANTOS C, MARTMEZ-HERNANDEZ A L, FISHER F T, et al. Improvement of thermal and mechanical properties of carbon nanotube composites through chemical functionalization [J]. Chemistry of Materials, 2003, 15: 4470-4475.
    [56]KUMAR S, DANG T D, ARNOLD F E, et al. Synthesis, structure, and properties of PBO/SWNT composites [J]. Macromolecules, 2002, 35: 9039-3943.
    [57]ZHAO C, HU G, JUSTICE R, et al. Synthesis and characterization of multi-walled carbon Nanotubes reinforced polyamide 6 via in situ polymerization [J]. Polymer, 2005, 46: 5125-5132.
    [58]GAO J, ITKIS M E, YU A, et al. Continuous spinning of a single-walled carbon nanotube-nylon composite fiber [J]. Journal of American Chemical Society, 2005, 127, 3847-3854.
    [59]PARK C, OUNAIES Z, WATSON K A, et al. Dispersion of single wall carbon nanotube by in situ polymerization under sonication [J]. Chemical Physics Letters, 2002, 364: 303-308.
    [60]ZHU J, KIM J, PENG H, et al. Improving the dispersion and integration of single-walled carbon Nanotubes in epoxy composites through functionalization [J]. Nano Letters, 2003, 3: 1107-1113.
    [61]GOJNY F H, SCHULTE K. Functionalization effect on the thermomechanical behavior of multi-wall carbon nanotube/epoxy composites [J]. Composite Science and Technology, 2004, 64: 2303-2308.
    [62]BANERJEE S, HEMRAJ-BENNY T, WONG S S. Covalent surface chemistry of single-walled carbon Nanotubes [J]. Advanced Materials, 2005, 17: 17-29.
    [63]VISWANATHAN G, CHAKRAPANI N, YANG H, et al. Single-step in situ synthesis of polymer-grafted single-wall nanotube composites [J]. Journal of AmericanChemical Society, 2003, 125: 9258-9259.
    [64]QIN S, QIN D, FORD W T, et al. Functionalization of single-walled carbon Nanotubes with polystyrene via grafting to and grafting from methods [J]. Macromolecules, 2004, 37: 752-757.
    [65]HWANG G L, SHIEH Y T, HWANG K C. Efficient load transfer to polymer-grafted multiwalled carbon nanotubes in polymer composites [J]. Advanced Functional Materials, 2004, 14: 487-491.
    [66]XIA H, WANG Q, QIU G. Polymer-encapsulated carbon nanotubes prepared through ultrasonically initiated in situ emulsion polymerization [J]. Chemistry of Materials, 2003, 15: 3879-3886.
    [67]TONG X, LIU C, CHENG H M, et al. Surface modification of single-walled carbon Nanotubes with polyethylene via in situ Ziegler-Natta polymerization [J]. Journal of Applied Polymer Science, 2004, 92: 3697-3700.
    [68]FU K, HUANG W, LIN Y, et al. Defunctionalization of functionalized carbon Nanotubes [J]. Nano Letters, 2001, 1: 439-441.
    [69]BLAKE R, GUN’KO Y K, Coleman J, et al. A generic organometallic approach toward ultra-strong carbon nanotube polymer composites [J]. Journal of American Chemical Society, 2004, 126: 10226-10227.
    [70]COLEMAN J N, BLAU W J, DALTON A B, et al. Improving the mechanical properties of single-walled carbon nanotube sheets by intercalation of polymeric adhesives [J]. Applied Physics Letters, 2003, 82: 1682-1684.
    [71]LAHIFF E, RYU C Y, CURRAN S, et al. Selective positioning and density control of Nanotubes within a polymer thin film [J]. Nano Letters, 2003, 3: 1333-1337.
    [72]MAMEDOV A A, KOTOV N A, PRATO M, et al. Molecular design of strong single-wall carbon nanotube/polyelectrolyte multilayer composites [J]. Natrue Materials, 2002, 1: 190-194.
    [73]OLEK M, OSTRANDER J, JURGA S, et al. Layer-by-layer assembled composites from multiwall carbon Nanotubes with different morphologies [J]. Nano Letters, 2004, 4: 1889-1895.
    [74]QIN S, QIN D, FORD W T, et al. Covalent crosslinked polymer/single-walled carbon nanotube multilayer films [J]. Chemistry of Materials, 2005, 17: 2131-2135.
    [75]VIGOLO B, PENICAUD A, COULON C, et al. Macroscopic fibers and ribbons of oriented carbon Nanotubes [J]. Science, 2000, 290: 1331-1334.
    [76]FORMHALS A. Inventor electrical spinning of fibers from solutions: US, 2123992 [P].1934
    [77]KO F, GOGOTSI Y, ALI A, et al. Electrospinning of continuous carbon nanotube-filled nanofiber yarns [J]. Advanced Materials, 2003, 15: 1161-1165.
    [78]SEN R, ZHAO B, PEREA D, et al. Preparation of single-walled carbon nanotube reinforced polystyrene and polyurethane nanofibers and membranes by electrospinning [J]. Nano Letters, 2004, 4: 459-464.
    [79]AJAYAN P M, STEPHAN O, COLLIEX C, et al. Aligned carbon nanotubes formed by cutting a polymer resin-nanotube composite [J]. Science, 1994, 265: 1212-1214.
    [80]TREACY M M, EBBESEN T W, GIBSON J M. Exceptionally high Yong's modulus observed for individual carbon nano-tubes[J ]. Nature, 1996, 381: 678-680.
    [81] WALTERS D A, ERCSON L M, CASAVANT M J, et al. Elastic strain of freely suspended single-wall carbon nanotube ropes [J]. Applied Physics Letters, 1999, 74, 3803-3805.
    [82]IIJIMA S, BRABEC C, MAITI A, et al. Structural flexibility of carbon nanotubes [J]. Journal of Chemical Physics, 1996, 104: 2089-2092.
    [83]王彪,王贤保,胡平安等.碳纳米管/聚合物纳米复合材料研究进展[J].高分子通报, 2002,12: 8-13.
    [84]QIAN D, DICKEY E C , ANDREWS R, et al. Load transfer and deformation mechanisms in carbon nanotube-polystyrene composites [J]. Applied Physics Letters, 2000, 76: 2868-2870.
    [85]ANDREWS R, JACQUES D, RAO A M, et al. Alignment of carbon nanotubes in a polymer matrix by mechanical stretching [J]. Applied Physics Letters, 1998, 73: 1197-1199.
    [86]AJAY G, SUSAN B SINNOTT. Effect of chemical functionalization on the mechanical properties of carbon Nanotubes [J]. Chemical Physics Letters, 1998, 295: 273-278.
    [87]SALVETAT J P, BRIGGS G A D, BONARD J M, et al. Elastic and shear moduli of single-walled carbon nanotube ropes [J]. Physical Review Letters, 1999, 82: 944-947.
    [88]GONG X, LIU J, BASKARAN S, et al. Surfactant-assisted processing of carbon nanotube/polymer composites[J]. Chemistry of Materials, 2000, 12: 1049-1052.
    [89]SHAFFER M S P, WINDLE A H. Fabrication and Characterization of CarbonNanotube/Poly(vinyl alcohol) Composites [J]. Advanced Materials, 1999, 11: 937-941.
    [90]JIN L, BOWER C, ZHOU O. Alignment of carbon nanotubes in a polymer matrix by mechanical stretching [J]. Applied Physics Letters, 1998, 73: 1197-1199.
    [91]HAGGENMULLER R, GOMMANS H, RINZLER A, et al. Aligned Single-Wall Carbon Nanotubes in Composites by Melt Processing Methods [J]. Chemical Physics Letters, 2000, 330: 219-225.
    [92]AJAYAN P, SCHADLER L, GIANNARES C, et al. Single-walled carbon nanotube-polymer composites: strength and weakness [J]. Advanced Materials, 2000, 12: 750-753.
    [93]COOPER C A, YOUNG E J, HALSALL M. Investigation into the deformation of carbon nanotubes and their composites through the use of raman spectroscopy [J]. Composites Part A: Applied Science and Manufacturing, 2001, 32: 401-411.
    [94]JIA Z, WANG Z, XU C, et al. Study on poly(methyl methacrylate)/carbon nanotube composites [J]. Materials Science & Engineering A, 1999, 271: 395-400.
    [95]LOURIE O, WAGNER H D. Transmission electron microscopy observations of fracture of single-wall carbon nanotubes under axial tension [J]. Applied Physics Letters, 1998, 73: 3527-3529.
    [96]WAGNER H D, LOURIE O, Feldman Y. Stress-induced fragmentation of multiwall carbon nanotubes in a polymer matrix [J]. Applied Physics Letters, 1998, 72:188-190.
    [97]LOURIE O, WAGNER H D. Bulkling and collapse of embedded carbon nanotubes [J]. Physical Review Letters, 1998, 81: 1638-1641.
    [98]LOURIE O, WAGNER H D. Evidence of stress transfer and formation of fracture clusters in carbon nanotube-based composites [J]. Composites Science and Technology, 1999, 59: 975-977.
    [99]BOWER C, ROSEB R, JIN L, et al. Deformation of carbon nanotubes in nanotube-polymer composites [J]. Applied Physics Letters, 1999, 74: 3317-3319.
    [100]LORDI V, YAO N. Molecular mechanics of binding in carbonnanotube-polymer composites [J]. Journal of Materials Reseach, 2000, 15: 2770-2779.
    [101]WISE K, HINKLEY J. American Physical Society Spring Meeting, April 12~16, 2001 [C]. Seattle, WA: c2001.
    [102]HAMADA N, SAWADA S I, OSHIYAMA A. New one-dimensional conductors:Graphite microtubules [J]. Physical Review Letters, 1992, 68:1579-1581.
    [103]MINTMIRE J W, DUNLAP B I, WHITE C T. Are fullerene tubules metallic [J]. Physical Review Letters, 1992, 68: 631.
    [104]SAITO R, FUJITA M, DRESSELHAUS G, et al. Electronic structure of chiral graphene tububles [J]. Applied Physics Letters. 1992, 60: 2204-2206.
    [105]FRANK S, PONCHARAL P, WANG Z L, et al. Carbon nanotube quantum resistors[J]. Science, 1998, 280: 1744-1746.
    [106]LIANG W J, BOCKRATH M, BOZOVIC D, et al. Fabry-Perot interference in a nanotube electron waveguide [J]. Nature. 2001, 411: 665-669.
    [107]THESS A, LEE R, NIKOLAEV P, et al. Crystalline Ropes of Metallic Carbon Nanotubes [J]. Science, 1996, 273: 483-488.
    [108]BAUGHMAN R H, ZAKHIDOV A A, DE HEER W A. Carbon Nanotubes--the Route Toward Applications [J]. Science, 2002, 297: 787-792.
    [109]SANDLER J K W, KIRK J E, SHAFFER M S P, et al. Ultra-low electrical percolation threshold in carbon-nanotube-epoxy composites [J]. Polymer, 2003, 44: 5893-5899.
    [110]SANDLER J, SHAFFER M S P, PRASSE T, et al. Development of a dispersion process for carbon nanotubes in an epoxy matrix and the resulting electrical properties [J]. Polymer, 1999, 40: 5967-5971.
    [111]DU F, FISCHER J E, WINEY K I. Coagulation method for preparing single-walled carbon nanotube/poly(methyl methacrylate) composites and their modulus, electrical conductivity, and thermal stability [J]. Journal of Polymer Science, Part B, 2003, 41: 3333-3338.
    [112]MICKELSON E T, HUFFMAN C B, RINZLER A G, et al. Fluorination of single-wall carbon Nanotubes [J]. Chemical Physics Letters, 1998, 296: 188-194.
    [113]STEVENS J K, HUANG A Y, PENG H, et al. Sidewall Amino-Functionalization of Single-Walled Carbon Nanotubes through Fluorination and Subsequent Reactions with Terminal Diamines [J]. Nano Letters, 2003, 3: 331-336.
    [114]SUNG J H, KIM H S, JIN H J, et al. Nanofibrous Membranes Prepared by Multiwalled Carbon Nanotube/Poly(methyl methacrylate) Composites [J]. Macromolecules, 2004, 37: 9899-9902.
    [115]PARK S J, CHO M S, LIM S T, et al. Synthesis and dispersion characteristics of multi-walled carbon nanotube composites with poly(methyl methacrylate) prepared by in-situ bulk polymerization [J]. Macromolecular Rapid Communication, 2003, 24: 1070-1073.
    [116]SHAFFER M S P, KOZIOL K. Polystyrene grafted multi-walled carbon nanotubes [J]. Chemical Communications, 2002, 2074-2075.
    [117]RAMASUBRAMANIAM R, CHEN J, LIU H. Homogeneous carbon nanotube/polymer composites for electrical applications [J]. Applied Physics Letters, 2003, 83: 2928-2930.
    [118]STRANO M S, MOORE C M, MILLER M K, et al. The role of surfactant adsorption during ultrasonication in the dispersion of single-walled carbon Nanotubes [J].Journal of Nanoscience and Nanotechnology, 2003, 3: 81-86.
    [119]ISLAM M F, ROJAS E, BERGEY D M, et al. High Weight Fraction Surfactant Solubilization of Single-Wall Carbon Nanotubes in Water[J]. Nano Letters, 2003, 3: 269-273.
    [120]BANDHYOPADHYAYA R, NATIV-ROTH E, REGEV O, et al. Stabilization of Individual Carbon Nanotubes in Aqueous Solutions [J]. Nano Letters, 2002, 2: 25-28.
    [121]SHVARTZMAN-COHEN R, LEVI-KALISMAN Y, NATIV-ROTH E, et al. Approach for dispersing SWNTs: the strength of a weak interaction [J]. Langmuir, 2004, 20: 6085-6088.
    [122]SZLEIFER I, YERUSHALMI-ROZEN R. Polymers and carbon nanotubes--dimensionality, interactions and nanotechnology [J]. Polymer, 2005, 46: 7803-7818.
    [123]REGEV O, EI KATI P N B, LOOS J, et al. Preparation of Conductive Nanotube–Polymer Composites Using Latex Technology [J]. Advanced Materials, 2004, 16: 248-251.
    [124]GRUNLAN J C, MEHRABI A R, BANNON M V, et al. Water-Based Single-Walled-Nanotube-Filled Polymer Composite with an Exceptionally Low Percolation Threshold [J]. Advanced Materials, 2004, 16: 150-153.
    [125]BARRAZA H J, POMPEO F, O’REAR E A, et al. SWNTs-filled thermoplastic and elastomeric composites prepared by miniemusion polymerization [J]. Nano Letters, 2002, 2:, 797-802.
    [126]Grossiord N, Loos J, Koning C E. Strategies for dispersing carbon nanotubes in highly viscous polymers [J]. Journal of Material Chemistry, 2005, 15: 2349-2352.
    [127]MAC DIARMID A G. Polyaniline and polypyrrole: where are we headee?[J]. Synthetic Metals, 1997, 84: 27-34.
    [128]LI Y F, OUYANG J, YANG J. 2 doping structures and structrral anisotropyrevealed by the mass-loss and shrinkage of polypyrrole films on alkali treatment[J]. Synthetic Metals, 1995, 74: 49-53.
    [129]ION A, ION I, POPESCU A, et al. A gerrocene crown ether functionalized polypyrrole film electrode for the electrochemical recognition of barium and calcium cations [J]. Adv Mater, 1997, 9: 711-713
    [130]BAKHSHI A K. Electrically conducting polymers-from fundamental to applied-research [J]. Bull Mater Sci, 1995, 18: 469-495.
    [131]何天白,胡汉杰.功能高分子与新技术(第二版)[M].北京:花学工业出版社,2001. 77-84.
    [132]FAN J, WAN M, ZHU D, et al. Synthesis, characterizations, and physical properties of carbon nanotubes coated by conducting polypyrrole [J]. Journal of Applied Polymer Science, 1999, 74: 2605-2610.
    [133]GAO M, HUANG S, DAI L, et al. Aligned coaxial nanoweres of carbon nanotubes sheathed with conducting polymers [J]. Angewandte Chemie International Edition, 2000, 39: 3664-3667.
    [134]JUREWICZ K, DELPEUX S, BERTAGNA V, et al. Supercapacitors from nanotubes/polypyrrole composites [J]. Chemical Physics Letters, 2001, 347: 36-40
    [135]FRACKOWIAK E, JUREWICZ K, SZOSTAK K, et al. Nanotubular materials as electrodes for supercapacitors[J]. Fuel Processing Technology, 2002, 77-78: 213-219.
    [136]FRACKOWIAK E, JUREWICZ K, DELPEUX S, et al. Nanotular materials for supercapacitors [J]. Journal of Power Sources, 2001, 97-98: 822-825.
    [137]HUNGES M, SHAFFER M S P, RENOUF A C, et al. Electrochemical capacitance of nanotubes with polypyrrole [J]. Advanced Materials, 2002, 14: 382-385.
    [138]CHEN J H, HUANG Z P, WANG D Z, et al. Electrochemical synthesis of polypyrrole/carbon nanotubes composites using well-aligned carbon nanotubes arrays[J]. Applied Physics A, 2001, 73: 129-131.
    [139]CHEN J H, HUANG Z P, WANG D Z, et al. Electrochemical synthesis of polypyrrole films over each of well-aligned carbon Nanotubes [J]. Synthetic Metals, 2002, 125: 289-294.
    [140]MUSA I, BAXENDALE M, AMARATUNGA G A, et al. Properties of regioregular poly(3-octylthiophene)/multi-wall carbon nanotube composites [J]. Synthetic Metals, 1999, 102: 1250-1254.
    [141]KYMAKIS E, AMARATUNGA G A J. Single-wall carbon nanotube/conjugatedpolymer photovoltaic devices [J]. Applied Physics Letters, 2002, 80: 112-114.
    [142]FAN J H, WAN M X, ZHU D B, et al. Synthesis, characterizations, and physical properties of carbon nanotubes coated by conducting polypyrrole [J]. Journal of Applied Polymer Science, 1999, 74: 2605-2610.
    [143]FAN J H, WAN M X, ZHU D B, et al. Synthesis and properties of carbon nanotube-polypyrrole composites [J]. Synthetic Metals, 1999, 102: 1266-1267.
    [144]KRYSZEWSKI M. Heterogeneous conducting polymeric systems: dispersions, blends, crystalline conducting networks - an introductory presentation [J]. Synthetic Metals, 1991, 45: 289-296.
    [145]黄大庆,丁鹤雁,刘俊能.碳纳米管/导电聚苯胺纳米复合纤维的合成与表征[J]. 2003, 2: 164-169.
    [146]WESSLING B. Scientific and Commercial Breakthrough for Organic Metals [J] Synthetic Metals, 1997, 85: 1313-1318.
    [147]CURRAN S A, AJAYAN P M, BLAU W J, et al. A composite from poly(m-pyenylenevinylene-co-2,5-dioctoxy-p-phenylenevinylene) and carbon nanotubes: a novel material for molecular optoelectronics [J]. Advanced Materials, 1998, 10: 1091-1093.
    [148]COLEMAN J N, DALTON A B, CURRAN S, et al. Phase separation of carbon nanotubes and turbostratic graphite using a functional organic polymer [J]. Advanced Materials, 2000, 12L: 213-216.
    [149]MC CARTHY B, DALTON A B, COLEMAN J N, et al. Spectroscopic investigation of conjugated polymer/single-walled carbon nanotubes interactions [J]. Chemical Physics Letters, 2001, 350: 27-32.
    [150] MC CARTHY B, COLEMAN J N, CREW R, et al. A microscopic and spectroscopic study of interactions between carbon nanotubes and a conjugated polymer [J]. The Journal of Physics Chemistry B, 2002, 106: 2210-2216.
    [151]TANG B Z, XU H. Preparation, alignment, and optical properties of soluble poly(phenylacetylene)-wrapped carbon Nanotubes [J]. Macromolecules, 1999, 32: 2569-2576.
    [152]STAR A ,STODDART J F ,STEUERMAN D, et al . Preparation and Properties of Polymer-Wrapped Single-Walled Carbon Nanotubes [J]. Angewandte Chemie International Edition, 2001, 40: 1721-1725.
    [153]AGO H, PETRITSCH K, SHAFFER M S P, et al. Composites of Carbon Nanotubes and Conjugated Polymers for Photovoltaic Devices [J]. Advanced Materials, 1999, 11: 1281-1285.
    [154]JIN Z X, SUN X, XU G Q, et al. Nonlinear optical Properties of some polymer/muti walled carbon nanotube composites [J]. Chemical Physics Letters, 2000, 318: 505-510.
    [155]HUANG S M, MAU A W H, DAI L M, et al. Patterned growth of well-aligned carbon nanotubes: A soft-lithographic approach [J]. Journal of Physics Chemistry B, 2000, 104: 2193-2196.
    [156]HUANG S M, MAU A W H, DAI L M, et al. Patterned growth and contact transfer of well-aligned carbon nanotube films [J]. Journal of Physics Chemistry B, 1999, 103: 4223-4227.
    [157]RIGGS J E, GUO Z X, CARROLL D L, et al. Strong luminescence of solubilized carbon Nanotubes [J]. Journal of the American Chemical Society, 2000, 122: 5879-5880.
    [158]LIN Y, RAO A M, SADANADAN B, et al. Functionalizing multiplewalled carbon nanotubes with aminopolymers [J]. Journal of Physics Chemistry B, 2002, 106: 1294-1298.
    [159]CADEK M, COLEMAN J N, RYAN K P, et al. Reinforcement of polymers with Carbon Nanotubes: The Role of Nanotube Surface Area [J]. Nano Letters, 2004, 4: 353-356.
    [160]SHAFFER M S P, WINDLE A H. Fabrication and Characterization of Carbon Nanotube/Poly (vinyl alcohol) Composites [J]. Advanced Materials, 1999, 11: 937-941.
    [161]GEORGE T, ADI E. Dynamic Mechanical Study of the Factors Affecting the Two Glass Transition Behavior of Filled Polymers: Similarities and Different with Random Ionomers [J]. Macromolecules, 1996, 28: 6067-6077.
    [162]塑料检验方法标准汇编_1973: GB 1044-70.出版日期:1974年6月第1版页数:123
    [163]SANDLER J, SHAFFER M S P, PRASSE T, et al. Development of a dispersion process for carbon nanotubes in an epoxy matrix and the resulting electrical properties [J]. Polymer, 1999, 40:5967-5971.
    [164]KILBRIDE B E, COLEMAN J N, FRAYSSE J, et al. Experimental observation of scaling laws for alternating current and direct current conductivity in polymer carbon nanotube composite thin films [J]. Journal of Applied Physics, 2002, 92: 4024-4030.
    [165]HUMBLOT V, METHIVIER C, PRADIER C M. Adsorption of l-Lysine on Cu(110): A RAIRS Study from UHV to the Liquid Phase [J]. Langmuir, 2006, 22: 3089-3096.
    [166]CATHIE VG, COUZI M, DENTZER J, et al. Surface Characterizations of Carbon Multiwall Nanotubes: Comparison between Surface Active Sites and Raman Spectroscopy [J]. Journal of Physics Chemistry B, 2004, 108: 19361-19367.
    [167]DYKE C A, TOUR J M. Covalent Functionalization of Single-Walled Carbon Nanotubes for Materials Applications [J]. Journal of Physics Chemistry A, 2004, 108: 11151-11159.
    [168]TSANG S C, CHEN Y K, GREEN M L H. A simple chemical method of opening and filling carbon Nanotubes [J]. Nature, 1994, 372: 159-162.
    [169]SCHAEFGEN J R, FLORY P J. Synthesis of Multichain Polymers and Investigation of their Viscosities [J]. Journal of American Chemical Society, 1948, 70: 2709-2718.
    [170]贾志杰,徐才录,梁吉等.关于尼龙-6/碳纳米管复合材料的研究[J].新型碳材料, 1999, 14: 32-36.
    [171] ZHAO C G, HU G J, JUSTICE R, et al. Synthesie and Characterization of Multi-Walled Carbon Nanotubes Reinforced Polyamide 6 via In Situ Polymerization [J]. Polymer, 2005, 46: 5125-5132.
    [172]JR J G S, DELOZIER D M, CONNELL J W, et al. Carbon nanotube-conductive additive-space durable polymer nanocomposite films for electrostatic charge dissipation [J]. Polymer, 2004, 45: 6133-6142.
    [173]QU L, LIN Y, HILL DE, et al. Polyimide-functionalized carbon nanotubes: synthesis and dispersion in nanocomposite films [J]. Macromolecules, 2004, 37: 6055-6060.
    [174]BIN Y Z, KITANAKA M, ZHU D, et al. Development of highly oriented polyethylene filled with aligned carbon nanotubes by gelation/crystallization from solutions [J]. Macromolecules, 2003, 36: 6213-6219.
    [175]SCHUELER R,PETERMANN J, SCHULTE K, et al. Agglomeration and electrical percolation behavior of carbon black dispersed in epoxy resin [J]. Journal Applied Polymer Science 1997; 63: 1741-1746

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