Fick1 4 25
Fick1 4 25
Liquids - Fick 's law refers to two miscible liquids when they come into contact
and the diffusion takes place at a macroscopic point. Fabrication of semiconductor-
Diffusion equations Fick's law is used for the manufacture of integrated circuits.
Applications in food industries.
What is Fick's law in relation to respiration?
According to Fick's law, the rate of gas transfer across a tissue plane or membrane
(Vgas) is directly proportional to the difference in partial pressures of the gas on
the two sides of the membrane (P1 – P2) and the membrane's diffusing capacity
(DM).
Factors that affect Fick's law of diffusion are concentration gradient, distance of
diffusion, diffusion coefficient, and medium properties. For concentration gradient,
the higher the difference in concentration between two regions, the greater the rate
of diffusion there is.
Fick's law of diffusion active or passive?
Passive diffusion follows a concentration gradient, which relates to the transport of
molecules from a location of higher concentration to a site of lower concentration
without using chemical energy according to Fick's law of diffusion.
According to Fick’s law of diffusion,
“The molar flux due to diffusion is proportional to the concentration
gradient”.
Fick's first law : Movemenet of particles from high to low concentration
( diffusive flux) is directly proportional to the particles’s concentration
gradient.
J = - D dc/dx = - DC
Fick's second law : Prediction of change in concentration gradienet with the time
due to diffusion. C/ t = x 2C / 2x
circuit. R
I
V = IR
V
Fs = - f.v
Fs = 6 r v , --- Stokes law
f =6r
Fs = 6 r v
Fs = drag force, r = radius of sphers, = fluid viscosity, v = velocity of the sphere
Stoke's Law
The force that retards a sphere moving through a viscous fluid is directly
proportional to the velocity and the radius of the sphere, and the viscosity of the
fluid.
f = 6 π r η v, (f = viscous drag force)
D = k T/ f
f = frictional coefficient
Brownian motion and the mean square displacement (x2) of a particle undergoing
Brownian motion over time (t), where k is Boltzmann constant , T = absolute
temperature (K, kelvin), f = frictional coefficient and D is D = diffusion
coefficient.
2kT/ f = the thermal energy (kT) and the frictional force (f) acting on the particle.
Mdif =!Ddc dx"!Dc2!c1 x2!x1 =!P(c2!c1) Mdif =P(c1!c2) P=D ! Hücre Zarı © Prof. Dr. Ferit P
Basis of bioelectricity:
1) Diffusion
Stoke’s law: The force acting downward is equal to 4/3πr3 (d1 − d2)g, in
which d1 is the density of the sphere, d2 is the density of the liquid, and g is
the acceleration due to gravity. At a constant velocity of fall called the
terminal velocity, the upward and downward forces are in balance.
D = diffusion coefficient
dc / dx = concentration coefficient
(c2-c1 / x2-x1) = approximation of the concentration coefficient
P = permeablility, a measure of how easily flow a substance can pass a membrane
or
a barrier
-P (c2-c1): the flux is ------
Osmosis in membrane
P = h g
Osmotic pressure = v c RT = RT vi ri ci
vi .ci = osomolar ironconcentration , osmolarity
Osmotic pressure is defined as the minimum pressure applied to a solution to
stop the flow of solvent molecules through a semipermeable membrane . The
osmotic pressure of a solution is proportional to molar concentration of the solute
particles in the solution.
Osmolarity: the number of particles of solute per liter of solution, whereas the tem
osmolality refers to the number of particles of solute per kilpgram of solvent.
Osmolarity is an estimation of the osmolar concentration of plasma and is
proportional to the number of particles per litre of solution; it is expressed asa
mmol/ L.This is what is used when a calculated values is derived. It is derived
from the measured Na+ ,K+, urea and glucose concentration.
;
Osomotic pressure for the body fluids
Calculation 775 kPa
Experiment 736 kPa
Men activity coefficient r= 0.93
Free energy difference
The standard free energy change (ΔG°) can be calculated from the equilibrium constant (K)
using the following equation: ΔG° = -RT ln(K) where: - R is the universal gas constant (8.314
J/(mol·K) or 0.008314 kJ/(mol·K)) - T is the temperature in Kelvin - ln is the natural logarithm - K
is the equilibrium constant ...
Common symbols S
Gi = Gi in – Gi out