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Integrated analysis of modified Japanese cypress using solid-state NMR spectra and nuclear magnetic relaxation times

机译:用固态NMR光谱和核磁松弛时间对改进日本赛柏的综合分析

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摘要

Acetylation and resin impregnation of Japanese cypress and subsequent heating of these modified cypresses were examined using an integrated analysis of solid-state NMR spectra and relaxation times. The H-1 magic angle spinning NMR showed altered moisture balance after chemical and thermal modifications because of changed hydrophobicity. The C-13 cross-polarization/magic angle spinning (CP-MAS) NMR spectra showed that acetylation predominately occurred for carbohydrates while phenol formaldehyde (PF) and melamine formaldehyde (MF) resins permeated all biomass constituents in cypress samples. Spin-lattice relaxation times in the laboratory frame, T1H and T1C, increased with chemical modifications although T1C decreased with the curing of both resins. In contrast, H-1 spin-lattice relaxation in the rotation frame, T1 rho H, increased with the curing as well as acetylation. The tendencies of relaxation times with curing suggested that faster molecular motions were suppressed in the MHz frequency range, and slower molecular motions were enhanced in the kHz frequency range, which generally matched with the signal changes in the C-13 pulse saturation transfer/magic angle spinning NMR spectra. Scanning electron microscope observation showed different adhesion distribution between PF and MF resins, affecting the cellulose signals of C-13 CP-MAS NMR and T1H change due to the curing.
机译:使用固态NMR光谱和松弛时间的综合分析检查日本曲尿曲面的乙酰化和树脂浸渍以及随后的这些改性曲囊的加热。 H-1魔法角旋转NMR由于改变了疏水性而在化学和热改性后显示出改变的水分平衡。 C-13交叉偏振/魔角旋转(CP-MAS)NMR光谱表明,碳水化合物主要发生的乙酰化,而苯酚甲醛(PF)和三聚氰胺甲醛(MF)树脂渗透到冠状样品中的所有生物质成分。在实验室框架中,T1H和T1C的旋转晶格弛豫时间随化学修饰而增加,尽管T1C随着两种树脂的固化而降低。相反,旋转框架中的H-1旋转晶格弛豫T1 rhO H,随着固化和乙酰化而增加。具有固化的休闲时间的趋势表明,在MHz频率范围内抑制了更快的分子动作,并且在KHz频率范围内增强了较慢的分子动作,这与C-13脉冲饱和转移/魔法角度的信号变化匹配旋转NMR光谱。扫描电子显微镜观察显示PF和MF树脂之间的不同粘附性分布,影响C-13 CP-MAS NMR和T1H由于固化而变化的纤维素信号。

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