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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 °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” (~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,然后随着进一步超声处理而降低。原纤化过程对未原纤化氧化纸浆的热降解温度影响很小(降低6°C)。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,并在“高”(〜5 wt%)纳米原纤维负载下抑制了基质玻璃化转变。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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  • 来源
    《Cellulose》 |2009年第2期|227-238|共12页
  • 作者单位

    Macromolecular Science and Engineering Virginia Polytechnic Institute and State University 230 Cheatham Hall Blacksburg VA 24061-0323 USA;

    Department of Wood Science and Forest Products Virginia Polytechnic Institute and State University 230 Cheatham Hall Blacksburg VA 24061-0323 USA;

    Department of Wood Science and Forest Products Virginia Polytechnic Institute and State University 230 Cheatham Hall Blacksburg VA 24061-0323 USA;

    Department of Wood Science and Forest Products Virginia Polytechnic Institute and State University 230 Cheatham Hall Blacksburg VA 24061-0323 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    TEMPO; Sonication; Nanocomposites; Nanofibrils; Fibrillated; Cellulose;

    机译:速度;超声处理;纳米复合材料;纳米纤维;纤维化;纤维素;

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