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Contents

1. Introduction

9. Liquid Handling

2. Fluids

10.Microarrays

3. Physics of Microfluidic
Systems

11.Microreactors
12.Analytical Chips

4. Microfabrication Technologies
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13.Particle-Laden Fluids

5. Flow Control

a. Measurement Techniques

6. Micropumps
7. Sensors

b. Fundamentals of
Biotechnology

8. Ink-Jet Technology

c. High-Throughput Screening

Microfluidics - Jens Ducre

Fluids: Transport Phenomena

2. Fluids
2.1. General Characteristics
2.2. Dispersions
2.3. Thermodynamics
2.4. Transport Phenomena
2.5. Solutions
2.6. Surface Tension
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2.7. Electrical Properties


2.8. Optical Properties
2.9. Biological Fluids

Microfluidics - Jens Ducre

Fluids: Transport Phenomena

2.4. Transport Phenomena


2.4.1. Diffusion
2.4.2. Viscosity
2.4.3. Transport of Heat
2.4.4. Characteristic Numbers

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Fluids: Transport Phenomena

2.4 Summary of Phenomenological Laws


Transport processes
Arbitrary thermal motion on molecular level
Driven by gradients (inhomogeneities)
Mostly linear relationship
Flow = coefficient force

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2.4.1. Diffusion

Diffusion
Counteracts nonuniform particle densities
Thermal Brownian motion
Process underlying all other transport phenomena in fluids

Ficks first law

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Current density jN antiparallel to gradient


Systems seeks homogeneity
Diffusion coefficient D [m s-1]

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Fluids: Transport Phenomena

2.4.1. Diffusion
Ficks second law
Time domain
Fixed location

Combining Ficks first law and equation of continuity

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Laplace equation

Stationary conditions

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Fluids: Transport Phenomena

2.4.1 Molecular Picture


Derivation of diffusion constant D
Flow through surface z1
Between two planes with diverging
particle densities
Distance = mean free path lmfp
Particles reach plane without collisions
(statistically)
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Linear term of Taylor expansion


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Fluids: Transport Phenomena

2.4.1 Diffusion coefficient


Calculation of diffusion coefficient
Assumption: uniformly distributed directions of all vectors v

average over
Ensemble

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Fluids: Transport Phenomena

2.4.1 Examples for Diffusional Processes


Example
Bilateral diffusion from 2-D layer
Within pure solvent
Initial conditions

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Solution by educated guess

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Fluids: Transport Phenomena

2.4.1 Examples for Diffusive Processes

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2.4.1 Examples for Diffusive Processes

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2.4.1 Examples for Diffusive Processes

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2.4.1 Examples for Diffusive Processes

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2.4.1 Examples for Diffusive Processes

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2.4.1 Examples for Diffusive Processes


Example
Diffusion through permeable diaphragm
Initial conditions

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2.4.1. Laminar Mixing

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2.4.1 Time and Length Scales


Distance

2
(rules of thumb)

Time

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2
~l2/D

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2.4.1 Brownian Motion


Discovered by Scottish
Botanist Robert Brown
in 1827
Random thermal
motion of pollen under
microscope

Closely related to
thermal velocity

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Mesoscopic particle

Width of distribution
of particle locations

r0 = 1 m
m = 10-15 kg
T = 293 K
vT 3 mm s-1

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2.4.1 Brownian Motion

Fluorescent particles
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4 seconds of data
2 m in diameter
Left picture
Particles moving in pure water

Right picture shows


Particles moving in concentrated solution of DNA
I.e., in viscoelastic solution in other words
From http://www.deas.harvard.edu/projects/weitzlab/research/brownian.html

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2.4.1 Brownian Motion

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Erratic motion of single milk droplets in water


Droplets size of about 1 micrometer
Continuously kicked by fast-moving water molecules
Size 5000 times smaller

Magnification factor of about 10,000


http://www.microscopy-uk.org.uk/

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2.4.1 Boltzmann Distribution


System at T in thermal
equilibrium
Each particle with certain
kinetic energy
Potential gradient
Particles accumulate in
potential minimum

Counteracting diffusive current

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Boltzmann distribution
Ratio of particle densities Ni
at two locations separated by
potential difference E
Boltzmann function at T = 273 K
calibrated to N0 = 1

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2.4.1 Maxwell Distribution


Maxwell distribution
Fraction of molecules in
velocity interval [v, v + dv]
f(v)dv is probability of finding a vector v
in [v, v + dv]
Normalization of integrand function f(v) to
unity
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Leads to Maxwell distribution

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2.4.1 Maxwell Distribution


Transformation into energy
space
Replacing v with kinetic energy
E = 1/2 mv2

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Helps determining which fraction


of particles is capable of
jumping over a certain potential
energy barrier E0
Analytical expression for this
fraction

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2.4.1 Reaction Kinetics


Chemical Reactions
Binary collisions
Collision rate scales linearly with vT and thus with T1/2
Concentration of reaction partners c also influences speed of reaction
For single step reaction

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Reaction rate

- Governed by stoichiometry (x, y, ...)


Concentrations c(X), c(Y),
Reaction velocity constant kc
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2.4.1 Reaction Kinetics


Chemical reactions
Activation energy (Gibbs energy)
Simple model reaction

For simplicity: G = U = Eact


Typically Eact = 60 to 250 kJ mol-1
G = Gact Gact
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G < 0 exothermic
G > 0 endothermic

Velocity constant of reaction


Strongly dependent on T
Reaction-specific
Arrhenius equation

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2.4. Transport Phenomena


2.4.1. Diffusion
2.4.2. Viscosity
2.4.3. Transport of Heat
2.4.4. Characteristic Numbers

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2.4.2. Viscosity
Viscosity
Transfer of momentum from one plane sliding parallel to another
Mediated by fluid sandwiched between them
Internal friction of fluid

Newtons law of viscosity


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Relates flow of axial momentum pz = m vZ along lateral x-direction


from one plane sliding parallel to another one by viscosity
Unit of : Pa s = kg m-1 s-1 or old Poise with 1 Ps = 0.1 Pa s

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2.4.2 Viscosity of Gases


Assumptions for picture:
- Flow in z-direction
- Uniform particle density

Net flux in x-direction of longitudinal momentum pz

Newton
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Viscosity of gases

Kinematic viscosity
- Momentum diffusivity

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2.4.2 Viscosity of Gases

Order: 10-5 Pa s
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2.4.2 Viscosity of Liquids


Liquid
Very dense gas
lmfp average distance
between molecules
Macroscopic behavior governed
by intermolecular potentials

Picture
Moving A to A
Activation energy E0
External shear stress xz

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- Force f on each particle on wall


- f counteracts motion in
negative z-direction
- Momentum loss transferred to B
- Activation energy E = f a / 2

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2.4.2 Viscosity of Liquids


Transfer of momentum pZ = m vZ
Lateral velocity gradient

net difference between number of jumps +Z and -Z in


positive and negative z-direction, respectively
Evaluation of gradient (using Boltzmann Ansatz)
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0 fundamental oscillation frequency


of molecule between neighbors
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2.4.2 Viscosity of Liquids


First order Taylor expansion for E / kBT

Viscosity of liquids
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2.4.2 Viscosity of Liquids

Order: 10-3 Pa s
(gases: 10-5 Pa s)

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2.4.2 Newtonian Fluids


Newtonian fluids
Classical idealized fluids
Linear stress-strain relationship
I.e. linear relationship between tension tensor
and tensor of rate of deformation (strain rate)
- Viscosity : constant of proportionality

Approximated by gases and


simple liquids like water

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Non-Newtonian fluids
Dispersions containing large
structured macromolecules
E.g. polymers and proteins

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2.4. Transport Phenomena


2.4.1. Diffusion
2.4.2. Viscosity
2.4.3. Transport of Heat
2.4.4. Characteristic Numbers

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2.4.3. Transport of Heat


Equilibrium thermodynamics
System seeks uniform temperature distribution

Inhomogeneous T-distribution
Transport of heat

Two basic modes


Diffusion
- Statistical phenomenon (related to entropy)
- Summarized in macroscopic thermal conductivity
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Convection
- Far more complicated
- Macroscopic ramifications
- Minor importance in microworld

Another frequently encountered issue


Transfer of thermal energy at interface between two media/phases
No inter-phase diffusion / exchange of particles
Transmission and transition of heat
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2.4.3 Thermal Conductivity


Fouriers law
Basic equation quantifying diffusive transport of heat

Net flow of energy jQ


Thermal conductivity

Power

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Cross-section of flow A

Relaxation time for temperature gradient


Distance d
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2.4.3 Thermal Conductivity


Molecular picture
Net energy flow in positive z-direction
Using linear terms of Taylor-expansion

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2.4.3 Thermal Conductivity


Thermal conductivity

Approximating on lmfp

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Independent of particle density N for ideal gas

Heat diffusion coefficient


kinematic viscosity

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2.4.3 Thermal Conductivity


Typical values

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2.4.3 Convection

Macroscopic transport of particles


Characteristic for macro-devices
Important for heat transport in liquids and gases

Forced convection
Transport of heat by macroscopic particle flow
E.g., by an external mechanical source
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Free convection
For instance driven by buoyancy

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2.4.3 Convection

Convective currents
Stationary or non-stationary flow patterns

Simulation of convection
Often fail to coincide with experimental observations
E.g., atmospheric weather and climate
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Free Convection of minor importance in microdevices


Laminar conditions
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2.4. Transport Phenomena


2.4.1. Diffusion
2.4.2. Viscosity
2.4.3. Transport of Heat
2.4.4. Characteristic Numbers

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2.4.4. Characteristic Numbers


Fourier mass number
Characterizes diffusion

Time t, e.g. residence in chemical reaction chamber


Typical diffusive time scale tD = l2 / D
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Schmidt number
Relates viscosity and diffusion

Roughly 0.8 for gases

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2.4.4. Characteristic Numbers


Fourier number
Diffusion of heat
Stored thermal energy

Prandtl number

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Ratio between momentum diffusivity (via dynamic viscosity )


and heat diffusivity (via thermal conductivity )

Specific heat capacity Cm


Typically 3 to 300 for liquids and 0.7 to1.0 for gases
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