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Micro PIV

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Micro PIV An optical diagnostic technique for microfluidics (e.g. MEMS, biological tissues, inkjet printer head) Requirements: Measure instantaneously 103 - 104 vectors – PowerPoint PPT presentation

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Title: Micro PIV


1
Micro PIV
  • An optical diagnostic technique for microfluidics
  • (e.g. MEMS, biological tissues, inkjet printer
    head)
  • Requirements
  • Measure instantaneously 103 - 104 vectors
  • Spatial resolution of 1 - 10 mm
  • Wide velocity range 50 mm/s - 400 m/s
  • Accurate to within 3 full scale
  • References
  • Meinhart, Wereley and Santiago (1999)
  • Santiago et al. (1998)
  • Private communication

2
Video Microscopy
  • Mature technology in bio-medical fields
  • The smallest resolvable size
  • dp l/NA , NA (Numerical Aperture) n sinq
  • For comparison, recall diffraction limit for
    camera
  • ddiff 2.44l/(D/f)2.44l(f)
  • Microscopy PIV
  • Resolve particles of sub-microns Measurement of
    particle displacement
  • Image field 30300mm

n
q
dp
3
Micro PIV vs. PIV
  • 30 300 mm
  • 1 10 mm
  • 2 20 mm
  • Laser sheet thickness 1 mm
  • Field of View 30 300 mm
  • Vector Spacing 1 10 mm
  • Interrogation Cell 2 20 mm
  • (50 overlap)
  • min. 10 pairs of particles for correlation
  • Plane Thickness dz
  • Depth of Field of microscope 1mm

Shrink 1000 times
4
Tracer Particles
  • Regular PIV
  • Small enough to track flow, need to be
    detectable by the camera
  • Dp 3 30 mm
  • Micro PIV
  • Small--
  • Follow flow
  • Do not clog the device
  • Do not alter fluid property
  • But not too small--
  • Suppress Brownian motion
  • Generate enough light signal
  • Dp 0.3 0.7 mm

5
Challenges by Sub-micron Particles
  • 1. Optical Resolution need Dp 300 700 nm
  • (NdYAG l 500 nm)
  • Visible light 400 nm ----- 750 nm
  • If NA lt1, cannot resolve dp less than l
  • sin q lt1
  • n index of refraction between specimen
    objective
  • 2. Low Light Signal

6
Solutions
  • Oil immersion lens (n ? 1.5) to get NA gt1
  • NA 1.4 for 60x - 100x objectives
  • Fluorescence (epi-illumination, reflection)
  • dp lt l stronger signal
  • Differential Interference Contrast (DIC)
    microscopy
  • Shearing interference to highlight refraction
    change

7
Light Source and Camera
  • Mercury arc lamp
  • Exposure t 2 ms
  • Pulse delay Dt 100 ms
  • (Also depend on camera transfer)
  • Velocity up to 50 mm/s
  • Pulsed laser
  • (Dual NdYAG laser)
  • t 5 ns
  • Dt 500 ns
  • up to 1 m/s

Digital CCD Camera (1030 x 1300 x 12 bit cooled
interlined transfer can record back-to-back
images within 500 ns)
8
Data Processing
  • Correlation
  • Significant Noise
  • Out-of-plane motion
  • Brownian motion
  • Ensemble-averaging correlation technique
  • (average 20 instantaneous correlations)
  • Limited to steady or periodic flows

9
Example 1
  • Santiago et al. (1998)

10
Result
  • Santiago et al. (1998)

11
Example 2
  • Meinhart, Wereley and Santiago (1999)

12
Result
  • Meinhart, Wereley and Santiago (1999)

Ensemble-averaged velocity-vector field measured
in a 30 mm deep, 300 mm wide, 25 mm channel. The
spatial resolution is 13.6 mm x 4.4 mm away from
the wall, and 13.6 mm x 0.9 mm near the wall. A
50 overlap between interrogation spots yields a
velocity vector spacing of 450 nm in the
wall- normal direction near the wall
13
Inkjet Printer Head
  • Field of view 50 500 mm
  • Need objective lens working distance gt1mm (Cover
    Glass)
  • Smaller NA Larger particle size
  • ( 0.6) ( 0.7 mm)
  • Unsteady flow in the cycle of droplet ejection
  • need instantaneous or phase-averaged
    measurement

14
Basic Limitation of Micro PIV
  • DOF ( 1mm) limits to strictly 2D flow
  • Not only 2D vector map,
  • Out-of-plane motion can cause measurement to fail
  • Hence must select a plane with only 2D motion

PIV Plane
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