光谱学与光谱分析
光譜學與光譜分析
광보학여광보분석
SPECTROSCOPY AND SPECTRAL ANALYSIS
2010年
1期
105-108
,共4页
张敏%朱波%王成国%魏晗兴
張敏%硃波%王成國%魏晗興
장민%주파%왕성국%위함흥
拉曼光谱%碳纤维%微结构%电化学改性
拉曼光譜%碳纖維%微結構%電化學改性
랍만광보%탄섬유%미결구%전화학개성
Raman spectra%Carbon fiber%Microstructure%Electrochemical treatment
采用激光拉曼光谱研究了电化学改性处理过程中聚丙烯腈基碳纤维的表面微结构变化,分析了不同处理时间下碳纤维的一级拉曼光谱特性.结果表明:碳纤维的一级拉曼光谱可以拟合为4个峰,即D(D_1),G,D_2和D_3,表征碳纤维表面微结构变化的拉曼参数主要有D线和G线的积分面积比R(I_D/I_G),D_2线与G线的积分面积比I_(D_3)/I_G,D_3线与G线比I_(D_3)/I_G以及所有无序结构积分面积总和与G线积分面积的比值I_(D_S)/I_G.电化学处理后,碳纤维表面无序度增大,D线和G线交叠度减小,R增大,I_(D_3)/I_G增大,I_(D_2)/I_G减小.随着处理时间的增加,I_(D_S)/I_G不断增大,它与R值的变化趋势基本一致,并且可以更伞面表征碳纤维表面结构有序性的变化.因此,利用激光拉曼光谱可以研究电化学改性处理过程中碳纤维表面的微结构变化规律.
採用激光拉曼光譜研究瞭電化學改性處理過程中聚丙烯腈基碳纖維的錶麵微結構變化,分析瞭不同處理時間下碳纖維的一級拉曼光譜特性.結果錶明:碳纖維的一級拉曼光譜可以擬閤為4箇峰,即D(D_1),G,D_2和D_3,錶徵碳纖維錶麵微結構變化的拉曼參數主要有D線和G線的積分麵積比R(I_D/I_G),D_2線與G線的積分麵積比I_(D_3)/I_G,D_3線與G線比I_(D_3)/I_G以及所有無序結構積分麵積總和與G線積分麵積的比值I_(D_S)/I_G.電化學處理後,碳纖維錶麵無序度增大,D線和G線交疊度減小,R增大,I_(D_3)/I_G增大,I_(D_2)/I_G減小.隨著處理時間的增加,I_(D_S)/I_G不斷增大,它與R值的變化趨勢基本一緻,併且可以更傘麵錶徵碳纖維錶麵結構有序性的變化.因此,利用激光拉曼光譜可以研究電化學改性處理過程中碳纖維錶麵的微結構變化規律.
채용격광랍만광보연구료전화학개성처리과정중취병희정기탄섬유적표면미결구변화,분석료불동처리시간하탄섬유적일급랍만광보특성.결과표명:탄섬유적일급랍만광보가이의합위4개봉,즉D(D_1),G,D_2화D_3,표정탄섬유표면미결구변화적랍만삼수주요유D선화G선적적분면적비R(I_D/I_G),D_2선여G선적적분면적비I_(D_3)/I_G,D_3선여G선비I_(D_3)/I_G이급소유무서결구적분면적총화여G선적분면적적비치I_(D_S)/I_G.전화학처리후,탄섬유표면무서도증대,D선화G선교첩도감소,R증대,I_(D_3)/I_G증대,I_(D_2)/I_G감소.수착처리시간적증가,I_(D_S)/I_G불단증대,타여R치적변화추세기본일치,병차가이경산면표정탄섬유표면결구유서성적변화.인차,이용격광랍만광보가이연구전화학개성처리과정중탄섬유표면적미결구변화규률.
Laser Raman spectroscopy was employed to characterize the microstructure variations of polyacrylonitrile-based carbon fibers during electrochemical treatment, and the characteristics of first-order Raman spectra of carbon fibers with different treatment time were investigated in the present paper. The results indicate that the Raman spectra of the carbon fibers can be fitted into four bands, named as D (or D_1 ) band, G band, D_2 band and D_3 band, respectively. The Raman parameters to characterize surface microstructure variations of carbon fibers mainly include R(I_D/I_G, area ratio of D band and G band), I_(D_2) /I_G(area ratio of D_2 band and G band),I_(D_3) /I_G(area ratio of D_3 band and G band), and I_(D_S) /I_G(area ratio of all the disordered structure and G band). The peak separation between D band and G band becomes large after electrochemical treatment R increases, which indicates that the surface disordered degree of carbon fibers increases. I_(D_S) /I_G increases, which is caused by organic molecules, fragments or functional groups; decreases which is caused by the break of the aliphatic structures. With increasing treatment time, I_(D_S)/I_G increases continuously, and the change trend of I_(D_S)/I_G is consistent with that of R value, which can be used to comprehensively explain the variation of the surface structure of carbon fibers. So, the variety rules of the structure of carbon fibers can be investigated by laser Raman spectroscopy during electrochemical treatment.