Toward dynamic force calibration

Measurement ◽  
2009 ◽  
Vol 42 (7) ◽  
pp. 1039-1044 ◽  
Author(s):  
Yusaku Fujii
ACTA IMEKO ◽  
2020 ◽  
Vol 9 (5) ◽  
pp. 124
Author(s):  
Feng Tian ◽  
Xiao Yin ◽  
Bo Li

The accuracy between a dynamic force and a static force applied on a specimen by a fatigue machine is usually not the same. By establishing physical vibration models of fatigue machines, it is concluded that the error of a cyclic force is mainly caused by the inertial force of the vibration mass between the machine sensor and the specimen. After the inertial force is exactly corrected, the force displayed on the machine would be consistent with the real force on the specimen. A standard dynamic force calibration sensor (DFCS) with an inertial force correction method has been used to do calibration of fatigue testing machines in this paper. Compared with the replica test-piece method, the two calibration results are close to each other.


ACTA IMEKO ◽  
2016 ◽  
Vol 5 (1) ◽  
pp. 51 ◽  
Author(s):  
Nieves Medina ◽  
Jesús De Vicente ◽  
Jorge Robles

This paper describes the magnetic effects studied at CEM in their realization of a primary standard for dynamic force calibration using sinusoidal excitations of force transducers, although they can also affect any sensor with an electrical output mounted on an electrodynamic shaker. In this study the electromagnetic behaviour for the interaction between sensor and shaker or a similar source of magnetic fields is explained and a solution to minimise this interaction is also included.


2011 ◽  
Author(s):  
Feng Meng ◽  
Zhi min Zhang ◽  
Yue Zhang ◽  
Wei Zhang

2020 ◽  
Vol 17 (162) ◽  
pp. 20190580
Author(s):  
Thomas J. Böddeker ◽  
Stefan Karpitschka ◽  
Christian T. Kreis ◽  
Quentin Magdelaine ◽  
Oliver Bäumchen

Flagella and cilia are cellular appendages that inherit essential functions of microbial life including sensing and navigating the environment. In order to propel a swimming microorganism they displace the surrounding fluid by means of periodic motions, while precisely timed modulations of their beating patterns enable the cell to steer towards or away from specific locations. Characterizing the dynamic forces, however, is challenging and typically relies on indirect experimental approaches. Here, we present direct in vivo measurements of the dynamic forces of motile Chlamydomonas reinhardtii cells in controlled environments. The experiments are based on partially aspirating a living microorganism at the tip of a micropipette force sensor and optically recording the micropipette’s position fluctuations with high temporal and sub-pixel spatial resolution. Spectral signal analysis allows for isolating the cell-generated dynamic forces caused by the periodic motion of the flagella from background noise. We provide an analytic, elasto-hydrodynamic model for the micropipette force sensor and describe how to obtain the micropipette’s full frequency response function from a dynamic force calibration. Using this approach, we measure the amplitude of the oscillatory forces during the swimming activity of individual Chlamydomonas reinhardtii cells of 26 ± 5 pN, resulting from the coordinated flagellar beating with a frequency of 49 ± 5 Hz. This dynamic micropipette force sensor technique generalizes the applicability of micropipettes as force sensors from static to dynamic force measurements, yielding a force sensitivity in the piconewton range. In addition to measurements in bulk liquid environment, we study the dynamic forces of the biflagellated microswimmer in the vicinity of a solid/liquid interface. As we gradually decrease the distance of the swimming microbe to the interface, we measure a significantly enhanced force transduction at distances larger than the maximum extent of the beating flagella, highlighting the importance of hydrodynamic interactions for scenarios in which flagellated microorganisms encounter surfaces.


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