Abstract:Fourier transform infrared (FTIR) spectroscopy was used to study the chemical changes of masson pine (pinus massoniana lamb.) decayed by the brown-rot fungus Wolfiporia cocos (Schwein. ) Ryvarden & Gilbn. for different durations up to 23 weeks. The ratios of height of the lignin/holocellulose and holocellulose/lignin IR peaks were measured, and the klason lignin content and holocellulose content of the sound wood and brown-rotted wood with different level of decay were analyzed by wet chemical methods. The relationship between the two chemical components and the ratios of IR peak height was also established. FTIR spectra showed that, during the first 15 weeks of decay, the intensity of absorption bands at 1 736 and 1 372 cm-1 ascribed to holocellulose decreased gradually, accompanied by a successive increase in the intensity of band at 1 510 and 1 225 cm-1 ascribed to lignin. However, the intensities of holocellulose bands at 1 736 and 1 372 cm-1 had a little increase, and the intensities of lignin bands at 1 510 and 1 225 cm-1 had a very slight decrease after 15 weeks of decay. There was a very good correlation between the ratios of height of the lignin/holocellulose (I1 510/I1 736, I1 510/I1 372, I1 225/I1 736 and I1 225/I1 372)and the klason lignin content or holocellulose content. The coefficients of determination for the klason lignin content and the holocellulose content were 0.97-0.99 and 0.96-0.97, respectively. High coeffieients of determination were also obtained between the holocellulose/lignin peak height ratios and the holocellulose content(R2=0.96). The above results suggest that, in the system studied, the klason lignin content and holocellulose content of wood decayed to differnent levels could be determined with reasonable accuracy by the FTIR technology.
[1] CHI Yu-jie(池玉杰). Wood Decay and Wood Decay Fungi(木材腐朽与木材腐朽菌). Beijing: Science Press(北京: 科学出版社), 2003. 26. [2] Schwanninger M, Hinterstoisser B, Gradinger C, et al. Journal of Near Infrared Spectroscopy, 2004, 12: 397. [3] Yutaka Kataoka, Kondo Tetsuo. Macromolecules, 1998, 31: 760. [4] Faix O, Bremer J, Schmidit O, et al. Journal of Analytical and Applied Pyrolysis, 1991, 21: 147. [5] Korner S, Pecina H, Wienhaus O. Holz als Roh- und Werkstoff, 1990, 48: 413. [6] Popescu C M, Popescu M C, Vasile C. Carbohydrate Polymers, 2010, 79: 362. [7] Pandey K K, Pitman A J. Intemational Biodeterioration Biodegradation, 2003, 52: 151. [8] Pandey K K, Pitman A J. Journal of Polymer Science: Part A: Polymer Chemistry, 2004, 42: 2340. [9] Fackler K, Schwanninger M, Gradinger C, et al. Fems Microbiology Letters, 2007, 271: 162. [10] Ferraz A, Baeza J, Rodriguez J, et al. Bioresource Technology, 2000, 74: 201 [11] CHI Yu-jie(池玉杰). Scientia Silvae Sinicae(林业科学), 2005, 41: 136. [12] WANG Ke-qin, WANG Lan-ying, WANG Yong-bing(王克勤, 王兰英, 汪勇兵). China Paten(中国专利), ZL 03128016. 1, 2006. [13] Faix O. Holzforschung, 1991, 45(Suppl.): 21. [14] LI Jian(李 坚). Wood Spectroscopy(木材波谱学). Beijing: Science Press(北京: 科学出版社), 2003. 109. [15] LI Gai-yun, REN Hai-qing, QIN Te-fu, et al.(李改云, 任海青, 秦特夫, 等). Journal of Forestry Research(林业科学研究), 2009, 22: 592. [16] Faix O. Fourier Transform Infrared Spectroscopy. In: Lin S Y,Dence C W(Eds). Methods in Lignin Chemistry. Berlin: Springer Verlag, 1992. 102.