Preparation of aligned polyimide-based carbon nanofibers by electrospinning
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摘要: 均苯四甲酸二酐和二氨基二苯醚溶解在N,N-二甲基乙酰胺中,室温下聚合为聚酰胺酸。以聚酰胺酸溶液作为前驱体,在20 kV电压下静电纺丝,然后进行350 ℃热亚胺化处理可得到定向排列的聚酰亚胺纳米纤维,再于900 ℃炭化、3 000 ℃石墨化,得到均匀连续、定向排列的聚酰亚胺基炭纳米纤维,纤维直径约100 nm。结果表明,聚酰胺酸质量分数为20%的溶液电纺性能最佳,3 000 ℃石墨化处理后的炭纳米纤维具有典型的石墨结构。Abstract: Polyimide (PI) is a good carbon precursor owing to its high carbon yield and easy graphitization. PI nanofibers prepared by electrospinning were carbonized and graphitized to prepare aligned carbon nanofibers. Pyromelliticdianhydride and 4,4'-diaminodiphenyl ether were dissolved in N,N-dimethylacetamide at room temperature and stirred for 2 h to obtain a polyamide acid (PAA) solution, which was electrospun into aligned PAA nanofibers at 20 kV and collected by a rolling cylinder 18 cm below the needle with a rolling speed of 2 800 r/min. The PAA nanofibers were first imidized into the PI nanofibers at 350 ℃, then carbonized at 900 ℃ at a heating rate of 5 ℃/min and finally graphitized at 3 000 ℃ to obtain continuous and aligned polyimide-based carbon nanofibers. The PAA solution with a concentration of 20% was the most suitable for electrospinning. SEM characterization shows that the average diameter of the carbon nanofibers is around 100 nm. The carbon nanofibers after graphitization at 3 000 ℃ have a typical graphite structure.
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Key words:
- Carbon nanofiber /
- Electrospinning /
- Alignment
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Wang M X, Guo Z Y, Huang Z H, et al. NH3-activated carbon nanofibers for low-concentration NO removal at room temperature
[J]. Catalysis Communications, 2015, 62: 83-88.
Xu C, Du H, Li B, et al. Asymmetric activated carbon-manganese dioxide capacitors in mild aqueous electrolytes containing alkaline-earth cations
[J]. Journal of the Electrochemical Society, 2009, 156(6): A435-A441.
MAO Zong-qing, XU Cai-lu, YAN Jun, et al. Preliminary study on hydrogen storage in carbon nanofibers
[J]. New Carbon Materials, 2000, 1: 64-67. (毛宗强, 徐才录, 阎 军, 等. 碳纳米纤维储氢性能初步研究
[J]. 新型炭材料, 2000, 1: 64-67.)
Jiang J Z, Zhang R Q, Zhang A J. Status and development of high-temperature filter material
[J]. Light Industry Science and Technology, 2014(08): 37-38. (蒋吉众, 张如全, 张爱军. 高温过滤材料的现状及发展
[J]. 轻工科技, 2014, 8: 37-38.)
Gan L, Du H, Li B, et al. Enhanced oxygen reduction performance of Pt catalysts by nano-loops formed on the surface of carbon nanofiber support
[J]. Carbon, 2008, 46(15): 2140-2143.
Wang J G, Yang Y, Huang Z H, et al. MnO-carbon hybrid nanofiber composites as superior anode materials for lithium-ion batteries
[J]. Electrochimica Acta, 2015, 170: 164-170.
Liu C K. Research progress in electrospinning process
[J]. China Synthetic Fiber Industry, 2012, 2: 53-56. (刘呈坤. 静电纺丝技术的研究进展
[J]. 合成纤维工业, 2012, 2: 53-56.)
Yang Y, Jia Z D, Li Q, et al. Electrospinning and its applications
[J]. High Voltage Engineering, 2006, 11: 2223-2253. (杨 颖, 贾志东, 李 强, 等. 电纺丝技术及其应用
[J]. 高电压技术, 2006, 11: 91-95.)
Chronakis I S. Novel nanocomposites and nanoceramics based on polymer nanofibers using electrospinning process - A review
[J]. J Mater Process Technol, 2005, 167(2-3): 283-293.
Huang Z M, Zhang Y Z, Kotaki M, et al. A review on polymer nanofibers by electrospinning and their applications in nanocomposites
[J]. Compos Sci Technol, 2003, 63(15): 2223-2253.
DAI Yi-le, DAI Jian-feng, SUN Yi-bing, et al. Alignment of carbon nanotubes in ultra-long carbon nanotube polymethylmethacrylate composite nanofibers by electrospinning
[J]. New Carbon Materials, 2013, 2: 101-107. (戴怡乐, 戴剑锋, 孙毅彬, 等. 静电纺丝法实现CNTs在超长复合纳米丝中的定向排列
[J]. 新型炭材料, 2013, 2: 101-107.)
Inagaki M, Ohta N, Hishiyama Y. Aromatic polyimides as carbon precursors
[J]. Carbon, 2013, 61: 1-21.
Yudin V E, Goykhman M Y, Balik K, et al. Carbonization behaviour of some polyimide resins reinforced with carbon fibers
[J]. Carbon, 2000, 38(1): 5-12.
Yang K S, Edie D D, Lim D Y, et al. Preparation of carbon fiber web from electrostatic spinning of PMDA-ODA poly(amic acid) solution
[J]. Carbon, 2003, 41(11): 2039-2046.
Xuyen N T, Ra E J, Geng H Z, et al. Enhancement of conductivity by diameter control of polyimide-based electrospun carbon nanofibers
[J]. J Phys Chem B, 2007, 111(39): 11350-11353.
Inagaki M, Harada S, Sato T, et al. Carbonization of polyimide film "Kapton"
[J]. Carbon, 1989, 27(2): 253-257.
Zhong H L, Zhang Y J. Zhang M Y, et al. The Properties of non-woven membranes of polyimide under different thermal imidization temperature
[J]. Figer Composites, 2008, 3: 41-44. (仲红玲, 张玉军, 张明艳, 等. 不同亚胺化温度对聚酰亚胺无纺布膜性能的影响
[J]. 纤维复合材料, 2008, 3: 41-44.)
Sadezky A, Muckenhuber H, Grothe H, et al. Raman micro spectroscopy of soot and related carbonaceous materials: Spectral analysis and structural information
[J]. Carbon, 2005, 43(8): 1731-1742.
Pei X, Shen B, Zhang L, et al. Accelerating the graphitization process of polyimide by addition of graphene
[J]. Journal of Applied Polymer Science, 2015, 132(2): 41274.
Yan H, Mahanta N, Wang B, et al. Stuctural evolution in graphitization of nanofibers and mats from electospun polyimide-mesophase pitch blends
[J]. Carbon, 2014, 71: 303-318.
Sadezky A, Muckenhuber H, Grothe H, et al. Raman micro spectroscopy of soot and related carbonaceous materials: Spectral analysis and structural information
[J]. Carbon, 2005, 43(8): 1731-1742.
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