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Characterization of Chemically Modified Wood Fibers Using FTIR Spectroscopy for Biocomposites

机译:使用FTIR光谱对生物复合材料进行化学改性的木纤维的表征

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摘要

Chemical modifications of wood fibers (Lignocel (R) C120) were performed for biocomposite applications, and chemically modified wood fibers were analyzed by FTIR spectroscopy. NaOH treatment showed band shifts from Cell-I to Cell-II in FTIR spectra from 2902 cm(-1), 1425 cm-1, 1163 cm(-1), 983 cm(-1), and 897 cm(-1) to 2894 cm(-1), 1420 cm(-1), 1161 cm(-1), 993 cm(-1), and 895 cm(-1) and the change in peak height at 1111 cm(-1) and 1059 cm(-1) assigned for Cell-I structure. Si lane treatment showed peak changes at 1200 cm(-1) assigned as Si-O- C band, at 765 cm(-1) assigned as Si-C symmetric stretching bond, at 700 cm(-1) assigned as Si-O-Si symmetric stretching, and at 465 cm(-1) assigned as Si-O-C asymmetric bending. Benzoyl treatment resulted in an increase in the carbonyl stretching absorption at 1723 cm(-1) and in band characteristics of aromatic rings (1604 cm(-1) and 710 cm(-1)) and a strong absorption at 1272 cm(-1) for C-O band in aromatic ring.
机译:进行了木纤维的化学改性(Lignocel C120)以用于生物复合材料,并通过FTIR光谱分析了化学改性的木纤维。 NaOH处理在FTIR光谱中从2902 cm(-1),1425 cm-1、1163 cm(-1),983 cm(-1)和897 cm(-1)显示了从Cell-I到Cell-II的带移至2894 cm(-1),1420 cm(-1),1161 cm(-1),993 cm(-1)和895 cm(-1)以及1111 cm(-1)处的峰高变化和分配给Cell-I结构的1059 cm(-1)。 Si通道处理显示在分配为Si-O-C波段的1200 cm(-1),分配为Si-C对称拉伸键的765 cm(-1),分配为Si-O的700 cm(-1)处的峰变化-Si对称拉伸,并在465 cm(-1)处分配为Si-OC不对称弯曲。苯甲酰处理导致羰基拉伸吸收在1723 cm(-1)和芳环(1604 cm(-1)和710 cm(-1))的带特征增加以及在1272 cm(-1)有很强的吸收)表示芳环中的CO带。

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