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浸渍银纳米悬浮液的热改性山毛榉木材的物理和力学性能及其与纤维素结晶度的关系

Physical and Mechanical Properties of Thermally-Modified Beech Wood Impregnated with Silver Nano-Suspension and Their Relationship with the Crystallinity of Cellulose.

作者信息

Bayani Siavash, Taghiyari Hamid R, Papadopoulos Antonios N

机构信息

Department of Wood and Paper Science and Technology, College of Agriculture and Natural Resources, Science and Research Branch, Islamic Azad University, Tehran, Iran.

Wood Science and Technology Department, Faculty of Materials Engineering & New Technologies, Shahid Rajaee Teacher Training University, Tehran, Iran.

出版信息

Polymers (Basel). 2019 Sep 20;11(10):1538. doi: 10.3390/polym11101538.

Abstract

The aim of this study was to investigate the physical and mechanical properties of thermally modified beech wood impregnated with silver nano-suspension and to examine their relationship with the crystallinity of cellulose. Specimens were impregnated with a 400 ppm nanosilver suspension (NS); at least, 90% of silver nano-particles ranged between 20 and 100 nano-meters. Heat treatment took place in a laboratory oven at three temperatures, namely 145, 165, and 185 °C. Physical properties and mechanical properties of treated wood demonstrated statistically insignificant fluctuations at low temperatures compared to control specimens. On the other hand, an increase of temperature to 185 °C had a significant effect on all properties. Physical properties (volumetric swelling and water absorption) and mechanical properties (MOR and MOE) of treated wood demonstrated statistically insignificant fluctuations at low temperatures compared to control specimens. This degradation ultimately resulted in significant decrease in MOR, impact strength, and physical properties. However, thermal modification at 185 °C did not seem to cause significant fluctuations in MOE and compression strength parallel to grain. As a consequence of the thermal modification, part of amorphous cellulose was changed to crystalline cellulose. At low temperatures an increased crystallinity caused some of the properties to be improved. Crystallinity also demonstrated a decrease in NS-HT185 in comparison to HT185 treatment. TCr indices in specimens thermally treated at 145 °C revealed a significant increase as a result of impregnation with nanosilver suspension. This improvement in TCr index resulted in a noticeable increase in MOR and MOE values. Other properties did not show significant fluctuations, suggesting that the effect of the increased crystallinity and cross-linking in lignin was more than the negative effect of the low cell-wall polymer degradation caused by thermal modification. Change of amorphous cellulose to crystalline cellulose, as well as cross-linking in lignin, partially ameliorated the negative effects of thermal degradation at higher temperatures and therefore, compression parallel to grain and modulus of elasticity did not decrease significantly. Overall, it can be concluded that increased crystallinity and cross-linking in lignin can compensate for some decreased properties caused by thermal modification, but it would be significantly dependent on the temperature under which modification is carried out. Impregnating specimens with silver nano-suspension prior to thermal modification enhanced the effects of thermal modification as a result of improved thermal conductivity.

摘要

本研究的目的是调查浸渍了纳米银悬浮液的热改性山毛榉木材的物理和力学性能,并研究它们与纤维素结晶度之间的关系。试样用400 ppm的纳米银悬浮液(NS)进行浸渍;至少90%的纳米银颗粒粒径在20至100纳米之间。热处理在实验室烘箱中于三个温度下进行,即145、165和185°C。与对照试样相比,经处理木材的物理性能和力学性能在低温下显示出统计学上不显著的波动。另一方面,温度升高到185°C对所有性能都有显著影响。与对照试样相比,经处理木材的物理性能(体积膨胀和吸水性)和力学性能(抗弯强度和弹性模量)在低温下显示出统计学上不显著的波动。这种降解最终导致抗弯强度、冲击强度和物理性能显著下降。然而,185°C的热改性似乎并未使弹性模量和横纹抗压强度产生显著波动。热改性的结果是,部分无定形纤维素转变为结晶纤维素。在低温下,结晶度的提高使某些性能得到改善。与HT185处理相比,NS-HT185中的结晶度也有所降低。在145°C下进行热处理的试样中的TCr指数显示,由于浸渍纳米银悬浮液而显著增加。TCr指数的这种提高导致抗弯强度和弹性模量值显著增加。其他性能未显示出显著波动,这表明结晶度增加和木质素交联的影响超过了热改性导致的细胞壁聚合物降解的负面影响。无定形纤维素向结晶纤维素的转变以及木质素中的交联,在一定程度上减轻了高温下热降解的负面影响,因此,横纹抗压强度和弹性模量并未显著降低。总体而言,可以得出结论,木质素中结晶度的增加和交联可以弥补热改性导致的一些性能下降,但这将很大程度上取决于进行改性的温度。在热改性之前用纳米银悬浮液浸渍试样,由于热导率的提高而增强了热改性的效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77b9/6835842/766a0d9bc3b7/polymers-11-01538-g001.jpg

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