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首页> 外文期刊>Cellulose >A new bio-based nanocomposite: fibrillated TEMPO-oxidized celluloses in hydroxypropylcellulose matrix
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A new bio-based nanocomposite: fibrillated TEMPO-oxidized celluloses in hydroxypropylcellulose matrix

机译:一种新的生物基纳米复合材料:羟丙基纤维素基质中的原纤化TEMPO氧化纤维素

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摘要

Utilization of TEMPO-oxidized celluloses in bio-based nanocomposites is reported for the first time. TEMPO-oxidized wood pulps (net carboxylate content 1.1 mmol/g cellulose) were fibrillated to varying degrees using a high intensity ultrasonic processor. The degree of fibrillation was controlled by varying sonication time from 1 to 20 min. The sonication products were then characterized independently and as fillers (5 wt% loading) in hydroxypropyl cellulose nanocomposite films. Nanofibril yields ranging from 11 to 98 wt% (on fiber weight basis) were obtained over the range of sonication times used. Suspension viscosities increased initially with sonication time, peaked with gel-like behavior at 10 min of sonication and then decreased with further sonication. The thermal degradation temperature of unfibrillated oxidized pulps was only minimally affected (6 A degrees C decrease) by the fibrillation process. Dynamic mechanical analysis of the nanocomposites revealed strong fibril-matrix interactions as evidenced by remarkable storage modulus retention at high temperatures and a suppression of matrix glass transition at "high" (similar to 5 wt%) nanofibril loadings. Creep properties likewise exhibited significant (order of magnitude) suppression of matrix flow at high temperatures. It was also believed, based on morphologies of freeze-fracture surfaces that the nanocomposites may be characterized by high fracture toughness. Direct fracture testing will however be necessary to verify this suspicion.
机译:TEMPO氧化纤维素在生物基纳米复合材料中的首次报道。使用高强度超声处理器将TEMPO氧化的木浆(净羧酸盐含量为1.1 mmol / g纤维素)原纤化。通过改变超声处理时间1至20分钟来控制原纤化程度。然后将超声处理产物分别表征为羟丙基纤维素纳米复合膜中的填充剂(5重量%)。在使用的超声处理时间范围内,获得的纳米原纤维产率为11至98重量%(基于纤维重量)。悬浮液粘度最初随超声处理时间而增加,在超声处理10分钟时达到凝胶样行为的峰值,然后随着进一步的超声处理而降低。未纤化的氧化纸浆的热降解温度受纤化过程的影响很小(降低了6 A摄氏度)。纳米复合材料的动态力学分析显示了强大的原纤维-基体相互作用,这在高温下具有显着的储能模量保持力,并且在“高”(约5 wt%)纳米原纤维负载下抑制了基质玻璃的转变。蠕变特性同样在高温下表现出显着(数量级)的基体流动抑制作用。还据认为,基于冷冻断裂表面的形态,纳米复合材料可以以高断裂韧性为特征。然而,必须进行直接的断裂测试以证实这种怀疑。

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