四川农业大学学报 ›› 2016, Vol. 34 ›› Issue (02): 178-184.doi: 10.16036/j.issn.1000-2650.2016.02.009

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樟和楠木的木材解剖结构特征和红外光谱比较研究

薛晓明1, 谢春平1, 孙小苗2, 南程慧1   

  1. 1. 南京森林警察学院, 国家林业局森林公安司法鉴定中心, 南京 210023;
    2. 国家林业局华东木材及木制品质量监督检验中心, 上海 200051
  • 收稿日期:2015-12-11 出版日期:2016-06-30 发布日期:2017-02-15
  • 作者简介:薛晓明,博士,副教授,从事珍稀植物保护、识别与鉴定工作,E-mail:jdmm24@me.com。
  • 基金资助:
    中央高校基本科研业务费专项资金项目(LGZD201405);江苏省高等教育教改研究课题(No.2013JSJG200);2014年度江苏省教育厅高校"青蓝工程"(苏教师[2014]23号)

Comparason on Anatomical Structure and FTIR Spectra between Cinnamomum camphora and Phoebe zhennan Woods

XUE Xiao-ming1, XIE Chun-ping1, SUN Xiao-miao2, NAN Cheng-hui1   

  1. 1. Nanjing Forest Police College/Forest Police Forensic Identification Center, The National Forestry Bureau, Nanjing 210023, China;
    2. East China Wood and Wood Products Quality Supervision and Testing Center of State Forestry Administration, Shanghai 200051, China
  • Received:2015-12-11 Online:2016-06-30 Published:2017-02-15

摘要: [目的] 以樟科的珍贵木材的樟木和楠木作为研究对象,探讨2种结构相近木材的有效识别方法。[方法] 通过光学显微镜和傅立叶红外光谱对二者的解剖结构、红外光谱特征分别进行了比较研究。[结果] 2种木材样本的显微结构特征较为相似,差异主要体现在樟木半散孔至散孔材,楠木为散孔材;樟木与楠木管孔平均弦径为(114.5293±31.5645)μm、(106.3788±19.6872)μm,樟木作为半散孔材平均弦径变化范围比楠木广。通过对6个木材样本的红外光谱比较,产地对樟木和楠木2种木材的红外光谱区域的指纹图谱有一定影响;2种木材的一维红外图谱峰形和出峰位置差异较小,仅在表征纤维素和半纤维素中C-O伸缩振动区域有所区别,樟木在波数1055 cm-1和1039 cm-1处形成了峰强度不等的双峰,楠木该位置只形成了波数1054 cm-1的一个不对称单峰;以1510 cm-1峰作为内标峰,与1595 cm-1(樟木)、1599 cm-1(楠木)的比值分别为1.1612和0.9969,说明樟木的木素中愈疮木基比例较高;樟和楠木的木材在波数800~1800 cm-1范围内的二阶导数谱差异明显,主要体现在吸收峰的数量和形状上,樟木的吸收峰可以分为17组峰簇,而楠木为17个独立吸收峰,全图谱的匹配度只有37.5。[结论] 分析产地因素,波数900~3400 cm-1区域为木材图谱特征稳定的区域,可用于2种木材的图谱区分;在1055 cm-1和1039 cm-1范围内吸收峰的形状、1595 cm-1(樟木)和1599 cm-1(楠木)和1510 cm-1峰的相对强度比,可以作为2种木材一维图谱的种间识别特征;2种木材的二阶导数图谱差别较大,可用于2种木材的区分。

关键词: 樟树, 楠木, 傅立叶红外光谱, 木素, 纤维素, 半纤维素, 二阶导数谱

Abstract: [Objective] The aim of the this paper was to establish an identification method for 2 woods(Cinnamomum camphora and Phoebe zhennan) with similar structure. [Method] Optical microscope and fourier transform infrared spectrometer(FTIR) were used in this study and anatomical structure and infrared spectroscopy characteristics were compared between the two woods. [Results] C. camphora and P. zhennan showed similar microstructure. C. camphora belonged to semi-diffuse-porous wood or diffuse-porous wood while P. zhennan belonged to diffuse-porous wood. The variation of C. camphora tangential diameter of pores was greater than that P. zhennan with average tangential diameter of(114.529 3±31.564 5) μm and(106.378 8±19.687 2) μm, respectively. According to FTIR comparison of 6 wood samples, the origin of woods have certain effects on finger-print FTIR. The infrared spectrum of two woods had a little difference in the peak shapes and peak positions, with distinction of C-O stretching vibration in cellulose and hemicellulose. The twin peaks of different peak intensity of C. camphora existed at 1 055 and 1 039 cm-1 while the asymmetric unimodal peak of P. zhennan existed at 1 054 cm-1. Taking the 1 510 peak as an internal standard peak, the rate of 1 595 cm-1(C. camphora) and 1 599 cm-1(P. zhennan) was 1.161 2 and 0.996 9, respectively, indicating that the C. camphora had a high ratio of guaiacyl group. The obvious differences in the second-derivative spectroscopy between C. camphora and P. zhennan was observed in the range of 800 cm-1 and 1 800 cm-1, which mainly existed in the number and shape of absorption peaks. The absorption peaks of C. camphora could be divided into 17 groups of peak cluster while P. zhennan with 17 independent absorption peaks, which only had 37.5 of matched-degree in the whole spectrum. [Conclusion] Based on the origin place, the stable FTIR between 900 and 3 400 cm-1 was used to characterize these two woods. The absorption shape of 1 055~1 039 cm-1 and relative intensity ratio of absorption peak of 1 595 cm-1(C. camphora), 1 599 cm-1(P. zhennan) and 1 510 cm-1 may be used to characterize these two woods. The second-derivative spectroscopy could be used to identify the two woods with obvious difference.

Key words: Cinnamomum camphora, Phoebe zhennan, fourier transform infrared spectroscopy, lignin, cellulose, hemicellulose, second derivative spectra

中图分类号: 

  • S572