scholarly journals Dynamic stiction without static friction: The role of friction vector rotation

2020 ◽  
Vol 102 (6) ◽  
Author(s):  
Ken Nakano ◽  
Valentin L. Popov
2003 ◽  
Vol 3 (4) ◽  
pp. 197-208
Author(s):  
Raoul Grönqvist ◽  
Simon Matz ◽  
Mikko Hirvonen

The variation in utilized and available friction over shoe-floor contact time was determined in the presence of high- and low-viscosity contaminants. The objectives were to improve the validity of slipperiness evaluations and to find better criteria for safe friction during heel strike. The utilized friction coefficients for six shoe types were determined during gait-trials with male participants. The available friction coefficients of these shoes were measured with a test rig simulating heel slipping. The experiments were performed on a stainless steel floor with concentrated glycerol ('oily' condition) and diluted glycerol (1:10 in water) as contaminants. It was hypothesized that any single friction measurement criterion would be an insufficient predictor for safe gait with no slip or with slip recovery, not leading to a fall. The results showed that both transitional friction (time-intervals from zero to about 250 ms of heel contact) and steady state kinetic friction (time-intervals from about 250 ms to 450 ms) properties in the shoe and floor interface play an important role in slipperiness measurement and slip/fall risk assessment. The role of static friction in the risk assessment remained unclear.


1992 ◽  
Vol 13 (4) ◽  
pp. 393-403 ◽  
Author(s):  
Henry R. Mushinsky ◽  
Carl Gans

AbstractThirteen sand skinks, Neoseps reynoldsi, were observed and videotaped traversing variously spaced plexiglass channels and spacings of pins to investigate locomotory patterns of a slender elongate lizard, with reduced limbs. Five individuals were recorded both before and after tail autotomy. Neoseps moves its limbs in locomotion on a flat surface; the hindlimbs participate in propulsion and their position, relative to their body, reflects the curvature of the trunk. Distance between pins, width of the plexiglass channel, and surface texture influence locomotory patterns. Individuals move more rapidly in wide channels, and movement is most irregular in channels with sandpaper floors. Whether on a plexiglass or a sandpaper floor, individuals travel more rapidly down the 2cm wide channel than the 1 cm channel. Fewer bends in the trunk in the wider channels may allow for more rapid movement. Autotomy of the tail slows movement on a plexiglass or sandpaper floor. The anterior portion of the tail contributes to the establishment of a static friction site that is jerked toward the head during locomotion, advancing the center of gravity in that direction. From the new site the trunk can be straightened by pushing against the friction site. The posterior portion of a tailless individual slides backward as the trunk is straightened, slowing their forward movement. The backward slide may reflect the lower mass and reduced static friction of the partial tail. In channels, Neoseps uses limbed concertina rather than simple concertina to generate a propulsive force. Evolutionarily, it appears that elongation of the tail and trunk did not incorporate the capacity for lateral undulation; as the curves of the trunk and tail seem preprogrammed and do not adjust to local points of contact.


2001 ◽  
Vol 64 (4) ◽  
Author(s):  
Henry Bock ◽  
Dennis J. Diestler ◽  
Martin Schoen

1975 ◽  
Vol 229 (5) ◽  
pp. 1400-1402 ◽  
Author(s):  
S Adelman ◽  
CR Taylor ◽  
NC Heglund

Man sweats on his palms and the soles of his feet in response to stress and exercise, but not in response to heat. Several functions have been proposed for this type of sweating: increasing friction between skin and substrate; increasing the toughness of the skin; and increasing tactile sensitivity. This study uses a comparative approach to evaluate the role of footpad sweating on increasing friction, utilizing a variety of mammals which possess sweat glands on their footpads (rat, tenrec, hyrax, and dog). We found that all of these animals sweat on their paws while running. Blocking this sweating with atropine sulfate dramatically decreased the coefficient of static friction between the paw and the tread of an inclined treadmill. A similar dose of atropine sulfate had no effect on the coefficient of static friction in a rabbit, and animal that possesses no sweat glands on its paws. We conclude that an important function of this type of sweating is to help prevent slipping between the paw and sthe substrate during running or climbing, and we postulate that the sweating observed in response to stress may play an important role in preparing an animal for fleeing from stressful situations.


JAMA ◽  
1966 ◽  
Vol 195 (12) ◽  
pp. 1005-1009 ◽  
Author(s):  
D. J. Fernbach
Keyword(s):  

JAMA ◽  
1966 ◽  
Vol 195 (3) ◽  
pp. 167-172 ◽  
Author(s):  
T. E. Van Metre

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