Nanotribology on a polymer network film

被引:13
作者
Haugstad, G
Gladfelter, WL
Jones, RR
机构
[1] UNIV MINNESOTA,DEPT CHEM,MINNEAPOLIS,MN 55455
[2] DUPONT CO INC,MED PROD DIV,BREVARD,NC 28712
来源
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A-VACUUM SURFACES AND FILMS | 1996年 / 14卷 / 03期
关键词
D O I
10.1116/1.580351
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Scanning force microscopy (SFM) of topography, frictional force, and stiffness on thin gelatin films reveals an entire spectrum of tribological behavior. Images display two distinct phases of gelatin whose characteristics relate to the degree of crystallinity. Dissimilar regimes of velocity- and load-dependent friction and wear on each phase indicate glassy, rubbery, or melt behavior. Of fundamental importance is the finding that energy transferred to the film in the vicinity of the sliding SFM microasperity modifies film response. Moderate frictional heating melts the highly crystalline phase, but reversibly induces rubbery behavior on the partially amorphous phase. More extreme frictional heating melts the latter and allows the liberated molecules to reassociate irreversibly into the highly crystalline phase. This relatively slow process (minutes) is imaged in real time on the submicron scale. Relaxation from rubbery to glassy behavior upon termination of perturbative scanning is extremely slow (hours) and also is characterized in frictional images. However, in this case the imaging process itself hastens the relaxation, apparently by providing energy to activate some relaxational processes. (C) 1996 American Vacuum Society.
引用
收藏
页码:1864 / 1869
页数:6
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