scholarly journals Characterization of flexure hinges for the French watt balance experiment

2014 ◽  
Vol 77 ◽  
pp. 00005 ◽  
Author(s):  
Patrick Pinot ◽  
Gérard Genevès
Keyword(s):  
2004 ◽  
Vol 75 (11) ◽  
pp. 4896-4905 ◽  
Author(s):  
Nicolae Lobontiu ◽  
Ephrahim Garcia ◽  
Mihail Hardau ◽  
Nicolae Bal
Keyword(s):  

Author(s):  
Maximilian Darnieder ◽  
Felix Harfensteller ◽  
Philipp Schorr ◽  
Moritz Scharff ◽  
Sebastian Linß ◽  
...  
Keyword(s):  

Author(s):  
P. Gournay ◽  
F. Villar ◽  
G. Geneves ◽  
C. Hauck ◽  
P. Juncar ◽  
...  

Author(s):  
F. Bielsa ◽  
A. Eichenberger ◽  
O. Gilbert ◽  
P. Juncar ◽  
G. Geneves
Keyword(s):  

2011 ◽  
Vol 221 ◽  
pp. 449-454
Author(s):  
Hua Wei Ji ◽  
Xiao Ping Hu

For its fast response, nanometer resolution, no backlash, no friction and bigger driving force, flexure hinge has been commonly used as a substitute for mechanical joints in the design of micro-displacement mechanisms used in vibration suppression and micro-positioning applications. However, inaccurate modeling of flexure hinges deteriorates the positioning accuracy. In this paper, a planar two-degree-of-freedom (DOF) parallel four-bar manipulator is designed with the intention of accurate flexure hinge modeling. A 1-DOF flexure hinge is considered, a static analysis and a dynamic analytical model of parallel four-bar manipulator is presented. Simulation result based on the finite element method is coincident to the analytic result. Based on the theoretical analysis, the experimental demonstration to study the performance of the manipulator is described, and experimental results are in close agreement with those predicted by the theoretical analysis.


Author(s):  
B. L. Soloff ◽  
T. A. Rado

Mycobacteriophage R1 was originally isolated from a lysogenic culture of M. butyricum. The virus was propagated on a leucine-requiring derivative of M. smegmatis, 607 leu−, isolated by nitrosoguanidine mutagenesis of typestrain ATCC 607. Growth was accomplished in a minimal medium containing glycerol and glucose as carbon source and enriched by the addition of 80 μg/ ml L-leucine. Bacteria in early logarithmic growth phase were infected with virus at a multiplicity of 5, and incubated with aeration for 8 hours. The partially lysed suspension was diluted 1:10 in growth medium and incubated for a further 8 hours. This permitted stationary phase cells to re-enter logarithmic growth and resulted in complete lysis of the culture.


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