期刊
APPLIED SURFACE SCIENCE
卷 455, 期 -, 页码 115-122出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.apsusc.2018.05.169
关键词
Superhydrophobic wood; Mechanical durability; Alkali-driven method; Chemical durability
类别
资金
- Key Laboratory of Bio-based Material Science AMP
- Technology, Ministry of Education [SWZCL2016-02]
- National Natural Science Foundation of China [31270602]
- Young Elite Scientists Sponsorship Program by CAST [2016QNRC001]
- Outstanding Innovative Youth Training Program of Changsha [KQ1707019]
- Hunan Provincial Technical Innovation Platform
- Talent Program in Science and Technology [2016RS2010, 2016TP1013]
Practical application of superhydrophobic wood remain a great challenge because of their poor durability and complicated production procedures. In this work, high-wear-resistance superhydrophobic wood was prepared by a facile, alkali-driven method using SiO2 nanoparticles (NPs) and vinyltriethoxysilane (VMS). The obtained wood had a contact angle (CA) of 156.6 degrees and a sliding angle (SA) of 1.8 degrees. It also exhibited a high tolerance to harsh mechanical damages such as sandpaper abrasion. The mechanical durability of material was intelligently controlled by tuning the amount of alkali. The results showed that the wood prepared using 24 mL of sodium hydroxide solution (0.1 mol/L) retained its original superhydrophobicity over an abrasion length of 270 cm, whereas that treated with the solution containing 6 mL of sodium hydroxide solution could only resist an abrasion length of 60 cm. Further examinations showed that the alkali treatment provides more hydroxyl groups on the wood surface. These hydroxyl groups readily catch hydrophobic SiO2 NPs, forming a rough hierarchical structure that supported by SiO2 NPs and micropores. The presence of the alkali ensures abundant SiO2 NPs anchoring on the wood substrate via chemical bonding, which contributes to the formation of a superhydrophobic coating with sufficient thickness and high bonding strength in support of mechanical stability.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据