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ChemWiki: The Dynamic Chemistry Hypertext > Core > Physical Chemistry > Kinetics > Rate Laws > Reaction Mechanisms > Rate of Diffusion through a Solution

Rate of Diffusion through a Solution

**Diffusion** in a gas is the random motion of particles involved in the net movement of a substance from an area of high concentration to an area of low concentration. Each particle in a given gas continues to collide with other particles. In regions of the gas where the particle density is the highest, the particles bounce off each other and the boundary of their container at a greater rate than particles in less-dense regions.

For a gas, the rate at which diffusion occurs is proportional to the square root of the density of the gas. The density of a gas is equal to the mass of the gas divided by the volume of the gas. If the volume is held constant one gas is compared with another with another,

\(\dfrac{R_2}{R_1} = \sqrt{\dfrac{M_1}{M_2}}\)

where R is the rate of diffusion in mol/s and M is the molar mass in g/mol. This is known as **Graham's law of diffusion.**

For a volume of solution that does not change:

\[J = -D\dfrac{dc}{dx}\]

- J is the flux, or movement, of the molecules in a given time interval denoted by units of moles/(time×area)
- D is the diffusivity constant, which describes the speed at which at object diffuses and has units of area/time
- Δc refers to the change in concentration from a point in time where no diffusion occurs to a point in time where the diffusion is complete, denoted by units of (moles/volume)
- Δx refers to the change in distance that a given particle undergoes during diffusion and has units of length.

Consider a cylinder with a region of high concentration and a region of low concentration. The volume of the region with no molecules can be designated as Area(of a circle) × L(length of the gap).

- The high concentration point on the left may be treated as \(C(X-1/2L)\)
- The low concentration point on the right may be treated as \(C(X+1/2L)\)

If the time interval is designated as ΔT, then:

- Average concentration coming from the left \(\propto C(X-1/2L) \times L \times Area \times \Delta{T}\)
- Average concentration coming from the right \(\propto C(X+1/2L) \times L \times Area \times; \Delta{T}\)

The total flux may be represented as:

\[J \propto \dfrac{[C(X-1/2L) \times L \times Area \times \Delta{T}] [C(X+1/2L) \times L \times Area \times \Delta{T}]}{(Area)(\Delta{T})}\]

Using the following relationship:

\(C(X+1/2L) = C(X)+1/2L \times \dfrac{dc}{dx}C(X-1/2L) = C(X)-1/2L \times \dfrac{dc}{dx}\)

Then:

\[J \propto -L^2\dfrac{dc}{dx}\]

L_{2} may be incorporated into the diffusivity constant D, and the equation for the flux may be rewritten as:

\[J = -D\dfrac{dc}{dx}\]

An incremental volume may have diffusion at both the rear and front surfaces of the volume. The rate at which the concentration changes with respect to the second derivative of the concentration gradient is given by the following formula:

\(\dfrac{\partial{C}}{\partial{T}} = x\dfrac{\partial ^2C}{\partial x^2}\)

If the front gradient allows (and thus drives) an uptake of solution into the incremental volume more quickly than the rear gradient allows for its dissipation, then the second derivative is positive. If the rear gradient allows for (and thus drives) the concentration out of the incremental volume more quickly than the front gradient allows for its uptake, then the second derivative is negative.

When two different particles end up near each other in solution, they may be trapped as a result of the particles surrounding them, which is known as the **cage effect** or **solvent cage**.

Two different particles colliding may be represented as a 2nd order reaction: \(A + B \rightarrow AB\)

\[AB = K_d[A][B]\]

Notice the use of K_{d} to denote the **diffusion rate constant**.

If circumstances change and either of the particles is able to diffuse out of the s**olvent cage**, then the following 1st order reaction \(AB \rightarrow A + B\) is possible, then:

\[AB = K_d'[AB]\]

There now exists a reaction for the formation of the AB complex as well as the breakdown of the AB complex into products.

\[k = \dfrac{K_aK_d}{K_a + K_d'}\]

\(V = K[A][B]\)

\[A + B \rightarrow AB \rightarrow Products\]

The net rate of formation for AB can now be determined:

\(\dfrac{d[AB]}{dt} = (A+B \rightarrow AB) - (AB \rightarrow A + B) - (AB \rightarrow Products)\)

\[\dfrac{d[AB]}{dt} = K_d[A][B] - K_d'[AB] - K_a[AB]\]

Assuming steady state conditions:

\[\dfrac{d[AB]}{dt} = K_d[A][B] - K_d'[AB] - K_a[AB] = 0\]

\([AB] = \dfrac{K_d[A][B]}{K_a + K_d'}\)

The final rate of product formation taking into account both **diffusion **and **activation**:

\(V = \dfrac{K_d[A][B]}{K_a + K_d'}\)

If the rate at which particle A encounters particle B is much slower than the rate at which AB dissociates, then Kd' is essentially zero.

\(V = \dfrac{K_d[A][B]}{K_a}\)

The rate at which particle A encounters and reacts with particle B may exceed the rate at which the AB complex breaks apart into a product by a significant quantity. If the rate of at which AB decomposes is slow enough that K_{a} in the denominator may be ignored, the following results:

\(V = \dfrac{K_d[A][B]}{K_d'}\)

Viscosity and rate of diffusion may be related by the following formula:

\(K_d = \dfrac{8RT}{3n}\)

where n is the viscosity of the solution.

- Compare the rate of diffusion between fluorine and chlorine gases. Fluorine gas, F
_{2}, has a molecular mass of 32 grams. Chlorine gas, Cl_{2}, has a molecular mass of 70.90 grams. - Gas A is 0.75 times as fast as Gas B. The mass of Gas B is 32 grams. What is the mass of Gas A?
- Determine the rate of diffusion (flux) for aspirin dissolving through the stomach lining. C
_{1}= 50 mg/L and C_{2}= 290 mg/L. The diffusivity constant of aspirin is 0.29×10^{-9}cm^{2}/s and the thickness of the stomach lining is approximately 0.5 cm. - How long will it take oxygen to diffuse 0.5 cm below the surface of a still lake if D = 1×10
^{-5}cm^{2}/s? - If it takes 5 seconds for oxygen to diffuse to the center of a bacterial cell that is 0.02 cm in diameter, determine the diffusivity constant.

1. Using Graham's law of diffusion:

(Rate_{1}/Rate_{2}) = (Mass_{2}/Mass_{1})^{1/2}

(RateF_{2}/RateCl_{2}) = (70.9g/32g)^{1/2} = **1.49**

**Fluorine gas is 1.49 times as fast as chlorine gas.**

2. Using Graham's law of diffusion:

(Rate_{1}/Rate_{2}) = (Mass_{2}/Mass_{1})^{1/2}

(Rate_{A}/Rate_{B}) = (Mass_{B}/Mass_{A})^{1/2}

0.75 = (32g/Mass_{A})^{1/2}

0.75^{2}=(32g/Mass_{A})

Mass_{A} = (32g/0.5625)

**Mass _{A} = 56.8888g**

3. Using Fick's first law:

J = -D(dc/dx)

Where:

J = unknown flux

D = 0.29×10^{-9} cm^{2}/s

dc = (C_{1} - C_{2}) = 50mg/L - 290mg/L = -240mg/L, which is equivalent to -240mg/1000cm^{3} =-0.24mg/cm^{3}

dx = 0.5cm

J = (0.29×10^{-9}cm^{2}/s)[(-0.24mg/cm^{3})/(0.5cm)] = 1.39×10^{-10}mg/s×cm^{2}

**J = 1.39×10 ^{-10}mg/s×cm^{2}**

4. Using Fick's second law:

T = x^{2}/2D

Where:

T = our unknown (time)

x = 0.5 cm

D = 1×10^{-5}cm^{2}/s

T = (0.5cm)^{2}/[2(1×10^{-5}cm^{2}/s)]

**T = 1.25×10 ^{4} seconds**

5. Using Fick's second law:

First, rearrange the equation T = x^{2}/2D to solve for D --> D = x^{2}/2T

Where:

D = our unknown (diffusivity constant)

x = 0.01 cm (distance from the outside to the center of the cell)

T = 5s

D = (0.01cm)^{2}/[2(5s)]

**D = 1×10 ^{-5}cm^{2}/s **

- Chang, Raymond. Physical Chemistry for the Biosciences. University Science Books, California 2005
- Atkins, Peter and de Paula, Julio. Physical Chemistry for the Life Sciences. W.H. Freeman and Company, New York 2005

- Eric Stouffer (UCD), Anne Slisz (UCD)

Last modified

03:27, 10 Jul 2015

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