Adhesion and friction mechanisms of polymer-on-polymer surfaces

被引:277
作者
Maeda, N
Chen, NH
Tirrell, M
Israelachvili, JN [1 ]
机构
[1] Univ Calif Santa Barbara, Coll Engn, Dept Chem Engn, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Coll Engn, Dept Mat, Santa Barbara, CA 93106 USA
[3] Univ Calif Santa Barbara, Coll Engn, Mat Res Lab, Santa Barbara, CA 93106 USA
关键词
D O I
10.1126/science.1072378
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The adhesion and friction of smooth polymer surfaces were studied below the glass transition temperature by use of a surface forces apparatus. The friction force of a crosslinked polymer was orders of magnitude less than that of an uncrosslinked polymer. In contrast, after chain scission of the outermost layers, the adhesion hysteresis and friction forces increase substantially. These results show that polymer-polymer adhesion hysteresis and friction depend on the dynamic rearrangement of the outermost polymer segments at shearing interfaces, and that both increase as a transition is made from crosslinked surfaces to surfaces with long chains to surfaces with quasi-free ends. The results suggest new ways for manipulating the adhesion and friction of polymer surfaces by adjusting the state of the surface chains.
引用
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页码:379 / 382
页数:4
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