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Rheological Properties of Chemically Modified Wood-Synthetic Polymer Blends

机译:化学改性木材合成聚合物共混物的流变性能

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The rheological properties in the melt state were investigated for several blends composed of butyrylated, caproylated or lauroylated wood and synthetic polymers, methyl methacrylate (MMA)-ethyl methacrylate (EA) copolymer and poly (methyl methacrylate) (PMMA). The results of viscoelastic measurements gave excellent time-temperature superposition for most of the blends. However, the superposition was not possible for blends with more than 90 % of the wood esters of higher aliphatic acids. Similar behavior is known for corresponding cellulose derivatives which are partially crystalline. The successful time-temperature superposition for the blends suggests the mutual plasticization among the derivatized wood components and also with the synthetic polymers in the blends. Also, it has been found that the better the compatibility of the chemically modified wood with synthetic polymer, the easier the occurrence of thermal flow, and the smaller the broadening of the second plateau, which is caused from the formation of higher ordered structures with longer relaxation times. In fact, the blend of butyrylated wood with MMA-EA copolymer, which shows the highest compatibility among samples used in this study, reveals the flow phenomenon within the range of the measurements, showing typical viscoelastic behavior starting from rubbery plateau to the flow. In the case of the blend of lauroylated wood with PMMA, which was confirmed to be a blend composed of two distinct phases, the viscoelastic properties of the blend sample became less temperature sensitive as the amount of lauroylated wood in the blend was increased. This trend can be understood by the reflection of the low temperature-dependent viscoelastic properties inherent in lauroylated wood. The compatibility of the chemically modified woods with synthetic polymer was measured on the corresponding films by the torsional-pendulum method, and evaluated in regard with the appearance of Tg, peaks in the logarithmic decrement-temperature curve. Furthermore, it was confirmed by the observation with a scanning electron microscope that the second plateau, which appears from the end parts of the rubbery plateau, broadens, when some fibrous residues of the chemically modified wood remain in the blend sample.
机译:研究了熔融状态的流变性质,用于几种共混物组成的丁酰基化,甲苯磺酸或月桂酸酯木和合成聚合物,甲基丙烯酸甲酯(MMA) - 甲基丙烯酸甲酯(EA)共聚物和聚(甲基丙烯酸甲酯)(PMMA)。粘弹性测量结果为大多数共混物提供了良好的时温度叠加。然而,具有超过90%的脂族酸的木材酯的混合物不可能进行叠加。相应的纤维素衍生物已知类似的行为,其是部分结晶的。共混物的成功时间 - 温度叠加表明衍生木组分的相互增塑以及共混物中的合成聚合物。此外,已经发现,较好地具有合成聚合物的化学改性木材的兼容性,热流量的发生越容易,第二平台的扩大越小,这是由较高有序结构的形成引起的放松时间。事实上,与MMA-EA共聚物的丁酰胺化木材的混合物显示出本研究中使用的样品中的最高相容性,揭示了测量范围内的流动现象,显示从橡胶状平坦到流动的典型粘弹性行为。在具有PMMA的月桂酸酯化木材的情况下,确认由两个不同相组成的共混物,混合样品的粘弹性变得较小,随着共混物中的月桂酸化合物的量而变得较小。通过桂茂木材固有的低温依赖性粘弹性特性的反射可以理解这种趋势。通过扭转摆方法在相应的膜上测量化学改性木材与合成聚合物的相容性,并在对数减量温度曲线中的Tg的外观进行评估。此外,通过用扫描电子显微镜观察,即第二平台,从橡胶状平坦的末端部分出现的第二平台,当化学改性木材的一些纤维残留物保留在混合物样品中时。

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