Shaped phase-plane control for flexible structures with friction

Author(s):  
C. La-orpacharapan ◽  
L.Y. Pao
1985 ◽  
Vol 8 (1) ◽  
pp. 50-55 ◽  
Author(s):  
Alexander N. Penchuk ◽  
Philip D. Hattis ◽  
Edward T. Kubiak

2004 ◽  
Vol 126 (1) ◽  
pp. 173-186 ◽  
Author(s):  
Lucy Y. Pao ◽  
Chanat La-orpacharapan

This paper describes the design of closed-loop control laws for servomechanisms with one dominant flexible mode. An input shaping technique is employed to alter the rigid body phase-plane trajectory that is used in time-optimal servomechanisms. The resulting controllers lead to near time-optimal performance without unwanted residual vibrations. After the basic technique is outlined for a system with one undamped flexible mode, extensions are given considering different acceleration and deceleration capabilities, damping, and slew rate limits.


2013 ◽  
Vol 19 (6) ◽  
pp. 1641-1645
Author(s):  
Ping Sun ◽  
Hongtao Zhao

2021 ◽  
Author(s):  
Zhihua Chen ◽  
Yongchun Xie ◽  
Yong Guo ◽  
Kai Zhang ◽  
Jinhua Guo ◽  
...  

Author(s):  
Ya Chen ◽  
Geoffrey Letchworth ◽  
John White

Low-temperature high-resolution scanning electron microscopy (cryo-HRSEM) has been successfully utilized to image biological macromolecular complexes at nanometer resolution. Recently, imaging of individual viral particles such as reovirus using cryo-HRSEM or simian virus (SIV) using HRSEM, HV-STEM and AFM have been reported. Although conventional electron microscopy (e.g., negative staining, replica, embedding and section), or cryo-TEM technique are widely used in studying of the architectures of viral particles, scanning electron microscopy presents two major advantages. First, secondary electron signal of SEM represents mostly surface topographic features. The topographic details of a biological assembly can be viewed directly and will not be obscured by signals from the opposite surface or from internal structures. Second, SEM may produce high contrast and signal-to-noise ratio images. As a result of this important feature, it is capable of visualizing not only individual virus particles, but also asymmetric or flexible structures. The 2-3 nm resolution obtained using high resolution cryo-SEM made it possible to provide useful surface structural information of macromolecule complexes within cells and tissues. In this study, cryo-HRSEM is utilized to visualize the distribution of glycoproteins of a herpesvirus.


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