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以含钴介孔分子筛为催化剂、乙醇为碳源,采用CVD法制备碳纳米管(CNTs)。通过原位合成法制备一系列不同碳纳米管含量的碳纳米管/羟基磷灰石(CNTs/HA)复合材料。分别采用XRD、FTIR、TEM、N2吸附一脱附和Raman光谱等分析手段,对所合成cNTs/HA复合材料的晶相、结构、形貌和比表面积等进行了表征。同时研究了碳纳米管的添加量对所合成cNTs/HA复合材料形貌的影响。XRD与Raman结果表明,所得CNTs/HA复合粉体中仅有CNTs与HA两种物相,纯度较高,结晶度较好;TEM结果显示,CNTs/HA复合材料中CNTs表面均匀包裹着一层纳米级的针状HA晶粒,两者形成了较强的界面结合,且当CNTs与HA的质量比为3:17时,CNTs与HA形成最佳结合状态;N2吸附一脱附表征结果表明,与HA的比表面积相比,CNTs/HA复合材料具有较高比表面积。

Carbon nanotuhes (CNTs) were prepared by chemical vapor deposition (CVD) method using Co- containing mesoporous molecular sieve as catalyst and ethanol as carbon source. A series of carbon nanotubes/ hydroxyapatite (CNTs/HA) composites with different amounts of CNTs were synthesized by using an in- situ method. The structure, morphology, crystal phase and the surface area of the as-synthesized CNTs/HA composites were characterized by XRD, FTIR, TEM, N2 physical adsorption - desorption and Raman spectroscopy. At the same time, the effect of CNTs on the morphology of the CNTs/HA composites was also investigated. XRD and Raman results show that CNTs/HA composites exhibit two kinds of crystal phases including CNTs and HA with good quality and crystallinity. TEM results reveal that the surface of CNTs was uniformly wrapped by nano-sized and needle-liked HA particles, and the good interfacial bonding exists between CNTs and HA. The optimal combination can be achieved between HA and CNTs when the mass ratio of CNTs to HA is 3 :17. N2 adsorption- desorption results indicate that CNTs/HA composites have high specific surface area as compared with HA.

参考文献

[1] Iijima S. Helical microtubules of graphitic carbon[J]. Nature, 1991, 354(6314): 56-58.
[2] Frackowiak E, Jurewicz K, Szostak K, et al. Nanotubular materials as electrodes for supercapacitors [J]. Fuel Proc Techn, 2002, 77/78: 213-219.
[3] 李维学,张胡军,戴剑锋,等.碳纳米管增强镁基复合材料热残余应力的有限元分析[J].复合材料学报,20i1,28(1):166-171
[4] Jiang Q, Qu Z M, Zhou G M, et al. A study of activated carbon nanotubes as electrochemical super capacitors electrode materials[J]. MaterLett, 2002, 57(4): 988-991.
[5] Bernier P, Maser W, Journet C, et al. Carbon single wall nanotubes elaboration and properties [J]. Carbon, 1998, 36 (5/6) : 675-680.
[6] Sheba R R J. Sorption behavior of Zn( Ⅱ ) ions on synthesized hydroxyapatites [J]. Colloid and Interface Science, 2007, 310(1) : 18-26.
[7] Jinwook K, Yunho S, Yongsug T. Growth of etchpits formed during sonoelectrochemical etching of aluminum [J]. Electrochimea Aeta, 2005, 51(5) : 1012-1016.
[8] Shepard S R, Jeffrey L, Koch G, et al. Diseoloration of ceramic hydroxyapatite used for protein chromatography [J]. Chromagraphy A, 2000, 891(1): 93-98.
[9] 卢志华,孙康宁,孙晓宁,等.碳纳米管的表面改性与羟基磷灰石的包覆[J].无机材料学报,2007,22(6):1127-1130.
[10] Zhao H Y, Zhou H M, Zhang J X, et al. Carbon nanotube- hydroxyapatite nanocomposite: A novel platform forglucose/ O2 biofuel cell [J]. Biosens and Bioelectronics, 2009, 25(2) : 463-468.
[11] 于志云,孙康宁,孙晓宁,等.纳米碳管/羟基磷灰石复合材料的凝胶注模[J].复合材料学报,2006,23(4):41-46.
[12] Jiang T S, Shen W, Zhao Q, et al. Characterization of CoMCM- 41 mesoporous molecular sieves obtained by microwave irradiation method [ J]. Journal of Solid State Chemstry, 2008, 181(9): 2298-2305.
[13] Zhao Q, Li Y H, Zhou X P, et al. Synthesis of multi- wall carbon nanotubes by the pyrolysis of ethanol on Fe/MCM - 41 mesoporous molecular sieves [ J ]. Superlattices and Mierostruetures, 2009, 47(3): 432-441.
[14] UematsuK, Takagi M, Honda T, et al. Transparent hydroxyapatite prepared by hot isostatic processing of filter cake[J]. J AmCeramSoc, 1989, 72(8): 1476-1478.
[15] Christa R. Calcium phosphate biomaterials and bone mineral [J]. Biomaterials, 1990, 11: 13-15.
[16] Boolchand P, Jin M I, Novita D I, et al. Raman scattering as a probe of intermediate phases in glassy networks [J]. Journal of Raman Spectroscopy, 2007, 38(3): 660-672.
[17] Popovie L, Waalde D, Boeyens J C A. Correlation between raman wavenumbers and P--O bond lengths in crystalline inorganic phosphates [J]. Journal of Raman Spectroscopy, 2005, 36(1): 2-11.
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