A Framework for Implementing Cooperative Motion on Industrial Controllers

2004 ◽  
Vol 20 (3) ◽  
pp. 583-589 ◽  
Author(s):  
B.M. Braun ◽  
G.P. Starr ◽  
J.E. Wood ◽  
R. Lumia
Keyword(s):  
Author(s):  
Fumikazu MINAMIYAMA ◽  
Hidetsugu KOGA ◽  
Kentaro KOBAYASHI ◽  
Masaaki KATAYAMA

1994 ◽  
Vol 172-174 ◽  
pp. 256-264 ◽  
Author(s):  
F.R. Blackburn ◽  
Marcus T. Cicerone ◽  
G. Hietpas ◽  
Paul A. Wagner ◽  
M.D. Ediger

Soft Matter ◽  
2021 ◽  
Author(s):  
Piotr Polanowski ◽  
Andrzej Sikorski

Monodisperse polymer brushes were studied by means of Monte Carlo simulations. A coarse-grained model of a polymer brush was designed in order and the Cooperative Motion Algorithm was employed to...


2018 ◽  
Vol 51 (29) ◽  
pp. 378-383 ◽  
Author(s):  
Marco Bibuli ◽  
Yogang Singh ◽  
Sanjay Sharma ◽  
Robert Sutton ◽  
Daniel Hatton ◽  
...  

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Masaki Hada ◽  
Daisuke Yamaguchi ◽  
Tadahiko Ishikawa ◽  
Takayoshi Sawa ◽  
Kenji Tsuruta ◽  
...  

Abstract The photoisomerization of molecules is widely used to control the structure of soft matter in both natural and synthetic systems. However, the structural dynamics of the molecules during isomerization and their subsequent response are difficult to elucidate due to their complex and ultrafast nature. Herein, we describe the ultrafast formation of higher-orientation of liquid-crystalline (LC) azobenzene molecules via linearly polarized ultraviolet light (UV) using ultrafast time-resolved electron diffraction. The ultrafast orientation is caused by the trans-to-cis isomerization of the azobenzene molecules. Our observations are consistent with simplified molecular dynamics calculations that revealed that the molecules are aligned with the laser polarization axis by their cooperative motion after photoisomerization. This insight advances the fundamental chemistry of photoresponsive molecules in soft matter as well as their ultrafast photomechanical applications.


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