6.021/Notes/2006-10-04: Difference between revisions
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===Combined transport=== | ===Combined transport=== | ||
Combining diffusion and drift to get Nernst-Planck Equation: | Combining diffusion and drift to get '''Nernst-Planck Equation''': | ||
<math>J_n = -z_nFD_n\frac{\partial c_n}{\partial x}-u_nz_n^2F^2c_n\frac{\partial\psi}{\partial x}</math> | <math>J_n = -z_nFD_n\frac{\partial c_n}{\partial x}-u_nz_n^2F^2c_n\frac{\partial\psi}{\partial x}</math> |
Latest revision as of 08:17, 11 October 2006
Ion Transport
- Major constituents of cells
- important functions
- charge is substrate for neural communication
- every charged particle (in principle) affects every other ion
- more complicated than other mechanisms
Mechanisms
2 distinct mechanisms of diffusion and drift
Diffusion
Given by Fick's law [math]\displaystyle{ \phi_n = -D_n\frac{\partial c_n}{\partial x} }[/math]
Drift
- Effect of electrical forces on montion of charged particles.
- Electric Field (vector field) [math]\displaystyle{ E(x,t) }[/math]
- force on particle [math]\displaystyle{ f_p = QE(x,t) = z_neE(x,t) }[/math] where [math]\displaystyle{ z_n }[/math] is valence and [math]\displaystyle{ e\approx 1.6\cdot 10^{-19} }[/math] C.
- Motions of small particles in water are viscosity dominated (Stokes 1855)
Forces | Size scale | Time scale |
inertial (F=ma) | [math]\displaystyle{ radius^3 }[/math] | acceleration |
viscosity | [math]\displaystyle{ radius }[/math] | velocity |
[math]\displaystyle{ v\propto f_p = u_p f_p = u_n f }[/math] where [math]\displaystyle{ u_p }[/math] is mechanical mobility in units of velocity/force, [math]\displaystyle{ u_n }[/math] is the molar mechanical mobility and [math]\displaystyle{ f }[/math] becomes the force on a mole of particle.
For charged particles: [math]\displaystyle{ v=u_nz_neN_AE(x,t)=u_nz_nFE(x,t) }[/math] ([math]\displaystyle{ F=eN_A }[/math] which is Faradya's number) = charge/mole about 96500 C/mol.
[math]\displaystyle{ D_n=u_nRT }[/math]: Einstein's relation
Flux due to drift: [math]\displaystyle{ \phi_n = \lim_{A\rightarrow 0 ; \Delta t\rightarrow 0}\frac{c_n(x,t)A\Delta x}{A\Delta t} = vc_n(x,t) }[/math]
[math]\displaystyle{ \phi_n = c_n(x,t)u_nz_nFE(x,t) = -c_nu_nz_nF\frac{\partial\psi}{\partial x} }[/math] where [math]\displaystyle{ E=-\frac{\partial\psi}{\partial x} }[/math] (electric field depends on the potential gradient)
The flux of ions is the current density given by [math]\displaystyle{ J_n = z_nF\phi_n }[/math] This is in units of current/area and is easier to measure than flux.
Combined transport
Combining diffusion and drift to get Nernst-Planck Equation:
[math]\displaystyle{ J_n = -z_nFD_n\frac{\partial c_n}{\partial x}-u_nz_n^2F^2c_n\frac{\partial\psi}{\partial x} }[/math]
Note that this is really just a combination of Fick's and Ohm's Laws.
Continuity: (needed to solve equations just like in other transport mechanisms)
[math]\displaystyle{ \frac{\partial\phi_n}{\partial x} = -\frac{\partial c_n}{\partial t} }[/math] or equivalently
[math]\displaystyle{ \frac{\partial J_n}{\partial x} = -z_nF\frac{\partial c_n}{\partial t} }[/math]
Unlike diffusion, also need one more equation for [math]\displaystyle{ \psi }[/math] but this electric potential depends on all particles.
From Gauss' law: [math]\displaystyle{ \frac{\partial E}{\partial x} = \frac{1}{\epsilon}\rho(x,t) = \frac{1}{\epsilon}\sum_n z_nFc_n(x,t) }[/math] where [math]\displaystyle{ \epsilon }[/math] is the permitivity and [math]\displaystyle{ \rho }[/math] is the charge density.
This leads to Poisson's Equation [math]\displaystyle{ \frac{\partial^2 \psi}{\partial x^2} = -\frac{1}{\epsilon}\sum_n z_nFc_n(x,t) }[/math]
Electroneutrality
- In a solution with some charge, after some time, all charges go to the edges away from each other.
- [math]\displaystyle{ \tau_r }[/math] is the relaxation time and is on the order of nanoseconds for physiological salines
- Similarly, in space, a region around the charge is formed that negates the charge. This is known as the Debye layer and has a thickness of around a nanometer.
- Thus for times much greater than the relaxation time and distances much greater than the Debye distance, we can assume electroneutrality of the solution.