环氧树脂
胶粘剂
固化(化学)
韧性
材料科学
单体
复合材料
脆性
流变学
剪切减薄
聚合物
图层(电子)
作者
Ammar Patel,Shekar Mekala,Oleksandr G. Kravchenko,Talha Yilmaz,Dian Yuan,Liang Yue,Richard A. Gross,Ica Manas‐Zloczower
出处
期刊:ACS Sustainable Chemistry & Engineering
[American Chemical Society]
日期:2019-09-18
卷期号:7 (19): 16382-16391
被引量:38
标识
DOI:10.1021/acssuschemeng.9b03489
摘要
We have successfully engineered a fast-curing, completely biobased epoxy adhesive that can exhibit lap shear strengths of above 20 MPa. The rigid, fast-curing, biobased epoxy monomer was co-polymerized with a flexible long-chain biobased monomer to increase toughness. The 60:40 weight ratio blend was identified for a nanoscale mixed morphology and an anomalous increase in mechanical properties and adhesive strength. The rheological behavior of the adhesive was further tuned by dispersing a biobased filler, cellulose nanocrystals (CNCs), into the optimized blend. The addition of CNC increased the curing rate, induced shear-thinning behavior, as well as further increased the adhesive strength. For 1 wt % and higher CNC fractions, filler network prevented the adhesive flow after application resulting in stable joints. Finally, the petroleum-derived curing agent was replaced with a biobased one (bis-(furfurylamine)) to cure the optimized resin formulation, resulting in stable crack growth and, thus, a dramatic change in fracture behavior. This brittle to ductile transition in fracture behavior corresponded to a significant increase in adhesive strength.
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