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Investigation of the wood/phenol-formaldehyde adhesive interphase morphology.

机译:木材/苯酚-甲醛粘合剂相间形态的研究。

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摘要

This work addresses the morphology of the wood/Phenol-Formaldehyde (PF) adhesive interphase or scale of PF penetration in wood. The objective is to develop methods for revealing ever smaller levels of wood/resin morphology. Dynamic techniques that are commonly utilized in polymer blend studies are implemented on wood/PF composites. These are Dynamic Mechanical Analysis (DMA) and solid state NMR using CP/MAS. PF resin molecular weight is manipulated to promote or inhibit resin penetration in wood, using a very low (PF-Low) or a very high (PF-High) molecular weight PF resin.; With DMA, the influence of PF resin on wood softening is investigated. It is first demonstrated that the cooperativity analysis according to the Ngai coupling model applies for wood softening. PF-Low does not influence wood softening temperature. However, intermolecular coupling is enhanced in the PF-Low composite, suggesting that PF-Low constrains wood relaxation. Surprisingly, PF-High significantly lowers the sample softening temperature. With CP/MAS NMR, none of the resins significantly affects the cross-polarization time (TCH), suggesting that angstrom scale penetration does not significantly occur. However, PF-Low alters wood polymer spin lattice relaxation time in the rotating frame, HT1rho, indicating nanometer scale interactions at the interphase. PF-High has no significant effect on wood HT1rho. Interestingly, PF-Low disrupts the spin coupling typical of wood components, while PF-High has no effect on spin coupling of wood components. Finally, the PF-Low resin T1rho lies within the range of wood relaxations suggesting spin coupling, while the PF-High resin T1rho appears outside the range of wood relaxations and is therefore not spin coupled with wood.; The CP/MAS NMR and DMA studies converge to identify nanometer scale penetration and in-situ cure of PF-Low in wood. On the other hand, PF-High forms overall separate domains from wood, although the low molecular weight tail of PF-High may penetrate wood on a nanoscale. The lower softening temperature in the PF-High composite may stem from this low molecular weight fraction penetrating wood intimately but remaining uncured or unconnected to the bulk PF-high resin phases.
机译:这项工作解决了木材/苯酚-甲醛(PF)胶粘剂相的形态或PF在木材中渗透的规模。目的是开发出揭示出越来越少的木材/树脂形态的方法。在木材/ PF复合材料中实施了聚合物共混研究中常用的动态技术。这些是使用CP / MAS的动态力学分析(DMA)和固态NMR。使用非常低(PF-低)或非常高(PF-高)分子量的PF树脂来控制PF树脂的分子量,以促进或抑制树脂在木材中的渗透。使用DMA,研究了PF树脂对木材软化的影响。首先证明,根据Ngai耦合模型进行的合作性分析适用于木材软化。 PF-Low不影响木材软化温度。但是,PF-Low复合材料的分子间偶联作用增强,表明PF-Low限制了木材的松弛。令人惊讶的是,PF-High显着降低了样品的软化温度。使用CP / MAS NMR,没有一种树脂会显着影响交叉极化时间(TCH),这表明不会显着发生埃级渗透。但是,PF-Low改变了旋转框架HT1rho中木材聚合物的自旋晶格弛豫时间,表明在相间存在纳米级相互作用。 PF-High对木材HT1rho没有明显影响。有趣的是,PF-Low破坏了木质部件的典型自旋耦合,而PF-High对木质部件的自旋耦合没有影响。最终,PF-低树脂T1rho处于木材弛豫范围内,表明发生了旋转耦合,而PF-高树脂T1rho出现在木材弛豫范围之外,因此未与木材发生旋转耦合。 CP / MAS NMR和DMA研究相结合,以鉴定纳米级渗透和木材中PF-Low的原位固化。另一方面,尽管PF-High的低分子量尾巴可能会以纳米级穿透木材,但PF-High与木材形成了整体上独立的区域。 PF-高复合材料的较低软化温度可能是由于这种低分子量组分紧密渗透木材,但仍未固化或未与本体PF-高树脂相连接。

著录项

  • 作者

    Laborie, Marie-Pierre G.;

  • 作者单位

    Virginia Polytechnic Institute and State University.;

  • 授予单位 Virginia Polytechnic Institute and State University.;
  • 学科 Chemistry Polymer.; Agriculture Wood Technology.
  • 学位 Ph.D.
  • 年度 2002
  • 页码 232 p.
  • 总页数 232
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 高分子化学(高聚物);森林采运与利用;
  • 关键词

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