Ground reaction force analysis of biped locomotion

2005 ◽  
Author(s):  
B. Yuksel ◽  
Changjiu Zhou ◽  
K. Leblebicioglu
Keyword(s):  
Ground Reaction Force ◽  
Reaction Force ◽  
Biped Locomotion ◽  
Force Analysis

Identification of subclinical tendon injury from ground reaction force analysis

1991 ◽  
Vol 23 (4) ◽  
pp. 266-272 ◽  
Author(s):  
S. M. DOW ◽  
J. A. LEENDERTZ ◽  
I. A. SILVER ◽  
A. E. GOODSHIP
Keyword(s):  
Ground Reaction Force ◽  
Reaction Force ◽  
Tendon Injury ◽  
Force Analysis

Ground reaction force analysis of large breed dogs when walking after the amputation of a limb

2000 ◽  
Vol 146 (6) ◽  
pp. 155-159 ◽  
Author(s):  
J. Kirpensteijn ◽  
R. van den Bos ◽  
W. E. van den Brom ◽  
H. A. W. Hazewinkel
Keyword(s):  
Ground Reaction Force ◽  
Reaction Force ◽  
Force Analysis

A ground reaction force analysis for designing a sustainable energy-harvesting stairway

2016 ◽  
Author(s):  
Debrina Puspitarini ◽  
Amalia Suzianti ◽  
Harun Al Rasyid ◽  
Nabila Priscandy
Keyword(s):  
Energy Harvesting ◽  
Ground Reaction Force ◽  
Sustainable Energy ◽  
Reaction Force ◽  
Force Analysis

Ground reaction force analysis as an aid to diagnosis of equine digital flexor tendon strain

1991 ◽  
Vol 24 (6) ◽  
pp. 450
Author(s):  
S.M. Dow ◽  
J.A. Leendertz ◽  
I.A. Silver ◽  
A.E. Goodship
Keyword(s):  
Ground Reaction Force ◽  
Flexor Tendon ◽  
Reaction Force ◽  
Force Analysis ◽  
Tendon Strain

Intramolecular Proton Transfer in the Isomerization of Hydroxyacetone: A Detailed Characterization Based on Reaction Force Analysis and the Bond Fragility Spectrum

2020 ◽  
Author(s):  
Wallace Derricotte ◽  
Huiet Joseph
Keyword(s):  
Chemical Potential ◽  
Reaction Force ◽  
Intramolecular Proton Transfer ◽  
Intermediate Energy ◽  
Force Analysis ◽  
Activation Energy Barrier ◽  
Detailed Characterization ◽  
Proton Transfers ◽  
Reaction Force Constant

The mechanism of isomerization of hydroxyacetone to 2-hydroxypropanal is studied within the framework of reaction force analysis at the M06-2X/6-311++G(d,p) level of theory. Three unique pathways are considered: (i) a step-wise mechanism that proceeds through formation of the Z-isomer of their shared enediol intermediate, (ii) a step-wise mechanism that forms the E-isomer of the enediol, and (iii) a concerted pathway that bypasses the enediol intermediate. Energy calculations show that the concerted pathway has the lowest activation energy barrier at 45.7 kcal mol<sup>-1</sup>. The reaction force, chemical potential, and reaction electronic flux are calculated for each reaction to characterize electronic changes throughout the mechanism. The reaction force constant is calculated in order to investigate the synchronous/asynchronous nature of the concerted intramolecular proton transfers involved. Additional characterization of synchronicity is provided by calculating the bond fragility spectrum for each mechanism.

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