首页 | 本学科首页   官方微博 | 高级检索  
     

炭纤维层间化合物的制备及其膨化(英文)
引用本文:M.Toyoda M.Inagaki 等. 炭纤维层间化合物的制备及其膨化(英文)[J]. 新型炭材料, 2002, 17(1): 1-3
作者姓名:M.Toyoda M.Inagaki 等
作者单位:[1]FukuiNationalCollegeofTechnology,Geshi,Sabae,Fuki916-8507,Japan [2]AichiInstituteofTechnology,Yakusa,Toyota470-0392,Japan
摘    要:在浓硝酸溶液(13mol/dm^3)中,通过恒电流电解,成功地进行了中间相沥青和聚丙烯腈基两种炭纤维(MPCF,PANCF)的硝酸插层。虽经水洗和干燥后有部分被分解成残余化合物,但从其层间距增至0.78nm左右这一现象证实已形成了层间化合物。经急剧加热至100℃后,观察到了显著的形貌变化,单根纤维沿着纤轴被劈裂开,转变成一束微纤维。低结晶度PAN-CF经急热处理后,被观察到了这种膨化现象。对经2000℃左右处理的MPCF,在两个阶段,电解时CF的电势明显增加:1500℃处理的MPCF电解电势逐渐增加,而1150℃处理的MPCF,此值几无上升。

关 键 词:层间化合物 电解 膨化炭纤维 中间相沥青基炭纤维 聚丙烯腈基炭纤维

PREPARATION OF INTERCALATION COMPOUNDS OF CARBON FIBERS AND THEIR EXFOLIATION
M.Toyoda,H.Katoh,A.Shimizu,M.Inagaki. PREPARATION OF INTERCALATION COMPOUNDS OF CARBON FIBERS AND THEIR EXFOLIATION[J]. New Carbon Materials, 2002, 17(1): 1-3
Authors:M.Toyoda  H.Katoh  A.Shimizu  M.Inagaki
Abstract:Intercalation of nitric acid into mesophase-pitch-based and PAN-based carbon fibers was successfully carried out by electrolysis of the fibers using a constant current in a concentrated nitric acid solution of 13mol/dm3. Formation of intercalation compounds was confirmed from the fact that the interlayer spacing increased to about 0.78nm, though a fraction decomposed to the residual compounds after rinsing and drying. After rapid heating to 1000℃, a marked morphological change was observed, a single fiber being converted to a bundle of thin filaments split along the original fiber axis. For PAN-based carbon fibers with low crystallinity, the exfoliation was observed after rapid heating. Potential change of carbon fibers during their electrolysis markedly increased in two steps for mesophase-pitch-based carbon fibers heat-treated above 2000℃. For carbon fibers treated at 1500℃, however, potential increased gradually, with almost no increase for those treated at 1150℃.
Keywords:Intercalation compounds  Electrolysis  Exfoliated carbon fibers  Mesophase pitch based carbon fibers  PAN based carbon fibers
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号