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Consider a narrow pipe filled with fluid, where the concentration of a specific type of molecule varies only along its length (in the x direction). Fick's second law is derived by considering the flux of these particles from both directions into a short segment∆x

∂n∂t=D∂2n∂x2

Short Answer

Expert verified

Consider a narrow pipe filled with fluid, where the concentration of a specific type of molecule varies only along its length (in the x direction). The Fick's second law is∂n∂t=D∂2n∂t2

Step by step solution

01

Step1:Explain type of molecule varies only along the length of the pipe 

The flux describes the rate at which molecules diffuse per unit area and per unit time in diffusion. Jx. Assume we have a narrow pipe filled with fluid or gas, and the molecular concentration varies only along its length. Take two adjacent narrow slices of pipe. each of widthΔx. The first slice is bounded byx1and x2and the second slice byx2and x3.

02

Step2:derive Fick's second law

Jx=−Ddndx(1)

The number of molecules entering sliceN12 from slice in time∆tis equal to the flux multiplied by the slice's cross sectional area and time interval, so:

N1=Jx,1AΔt

substitute fromJx=−Ddndx, so:

N1=−Dn2−n1ΔxAΔt(2)

Similarly, the number of molecules exiting the second slice on the opposite side, N2, is:

N2=−Dn3−n2ΔxAΔt(3)

The difference N1-N2is the net change in the number of molecules in the second slice, so:

ΔN=N1−N2(4)

subtract equation fromN1=−Dn2−n1ΔxAΔtandN2=−Dn3−n2ΔxAΔtsubstitute fromJx=−Ddndx

N1−N2=Dn3−n2ΔxAΔt−Dn2−n1ΔxAΔt

03

Step3:Solution

ΔNΔt=DAn3−n2Δx−n2−n1ΔxΔNΔt=DAn3−n2−n2+n1Δx→ΔNΔt=DAn3−2n2+n1Δx

dividing both sides by the slice's volumeV=AΔx, so:

ΔNVΔt=DAAΔxn3−2n2+n1Δx

utilizing molecular concentrationn=NVon the LHS we get:

ΔnΔt=Dn3−2n2+n1(Δx)2(5)

In the limit of,

Δt,Δx→0

In the following relation:

localid="1650264685606" ∂2y∂x2=y3−2y2+y1(Δx)2

will become

∂n∂t=D∂2n∂t2(6)

The solutions to this equation are the same as the solutions to the heat equation because they are formally equivalent. Starting with any concentration distribution, it will gradually spread out over time until the concentration is the same everywhere.

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Most popular questions from this chapter

Even at low density, real gases don’t quite obey the ideal gas law. A systematic way to account for deviations from ideal behavior is the virial

expansion,

PV−nRT(1+B(T)(V/n)+C(T)(V/n)2+⋯)

where the functions B(T), C(T), and so on are called the virial coefficients. When the density of the gas is fairly low, so that the volume per mole is large, each term in the series is much smaller than the one before. In many situations, it’s sufficient to omit the third term and concentrate on the second, whose coefficient B(T)is called the second virial coefficient (the first coefficient is 1). Here are some measured values of the second virial coefficient for nitrogen (N2):

T(K)
B(cm3/mol)
100–160
200–35
300–4.2
4009.0
50016.9
60021.3
  1. For each temperature in the table, compute the second term in the virial equation, B(T)/(V/n), for nitrogen at atmospheric pressure. Discuss the validity of the ideal gas law under these conditions.
  2. Think about the forces between molecules, and explain why we might expect B(T)to be negative at low temperatures but positive at high temperatures.
  3. Any proposed relation between P, V, andT, like the ideal gas law or the virial equation, is called an equation of state. Another famous equation of state, which is qualitatively accurate even for dense fluids, is the van der Waals equation,
    (P+an2V2)(V−nb)=nRT
    where a and b are constants that depend on the type of gas. Calculate the second and third virial coefficients (Band C) for a gas obeying the van der Waals equation, in terms of aand b. (Hint: The binomial expansion says that (1+x)p≈1+px+12p(p−1)x2, provided that |px|≪1. Apply this approximation to the quantity [1−(nb/V)]−1.)
  4. Plot a graph of the van der Waals prediction for B(T), choosing aand bso as to approximately match the data given above for nitrogen. Discuss the accuracy of the van der Waals equation over this range of conditions. (The van der Waals equation is discussed much further in Section 5.3.)

Calculate the total thermal energy in a gram of lead at room temperature, assuming that none of the degrees of freedom are "frozen out" (this happens to be a good assumption in this case).

Two identical bubbles of gas form at the bottom of a lake, then rise to the surface. Because the pressure is much lower at the surface than at the bottom, both bubbles expand as they rise. However, bubble A rises very quickly, so that no heat is exchanged between it and the water. Meanwhile, bubble B rises slowly (impeded by a tangle of seaweed), so that it always remains in thermal equilibrium with the water (which has the same temperature everywhere). Which of the two bubbles is larger by the time they reach the surface? Explain your reasoning fully.

The Fahrenheit temperature scale is defined so that ice melts at 320 F and water boils at 2120 F.

(a) Derive the formula for converting from Fahrenheit to Celsius and back

(b) What is absolute zero on the Fahrenheit scale?

Calculate the rms speed of a nitrogen molecule at room temperature.

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