Wallenberg Wood Science Center, KTH Royal Institute of Technology, Stockholm,
Biomacromolecules. 2012 Oct 8;13(10):3046-53. doi: 10.1021/bm300762e. Epub 2012 Sep 5.
For the first time the dry adhesion was measured for an all-wood biopolymer system using Johnson-Kendall-Roberts (JKR) contact mechanics. The polydimethylsiloxane hemisphere was successfully surface-modified with a Cellulose I model surface using layer-by-layer assembly of nanofibrillated cellulose and polyethyleneimine. Flat surfaces of cellulose were equally prepared on silicon dioxide substrates, and model surfaces of glucomannan and lignin were prepared on silicon dioxide using spin-coating. The measured work of adhesion on loading and the adhesion hysteresis was found to be very similar between cellulose and all three wood polymers, suggesting that the interaction between these biopolymers do not differ greatly. Surface energy calculations from contact angle measurements indicated similar dispersive surface energy components for the model surfaces. The dispersive component was dominating the surface energy for all surfaces. The JKR work of adhesion was lower than that calculated from contact angle measurements, which partially can be ascribed to surface roughness of the model surfaces and overestimation of the surface energies from contact angle determinations.
首次使用 Johnson-Kendall-Roberts (JKR) 接触力学测量了全木质生物聚合物系统的干附着。通过层层组装纳米原纤纤维素和聚乙烯亚胺,成功地对聚二甲基硅氧烷半球进行了纤维素 I 模型表面的表面改性。在二氧化硅衬底上同样制备了纤维素的平坦表面,并通过旋涂在二氧化硅上制备了葡甘露聚糖和木质素的模型表面。在加载过程中测量的粘附功和粘附滞后发现,纤维素与所有三种木质聚合物之间非常相似,这表明这些生物聚合物之间的相互作用没有很大差异。从接触角测量得出的表面能计算表明,模型表面的色散表面能成分相似。对于所有表面,色散分量均占主导地位。JKR 粘附功低于接触角测量计算的值,这部分可以归因于模型表面的表面粗糙度和接触角测定中表面能的高估。