The beauty of thermodynamics lies in its ability to connect macroscopic, observable quantities—like pressure, volume, and temperature—through elegant mathematical relationships. In this problem, we are presented with a monoatomic gas undergoing a specific thermodynamic process where its volume V is directly proportional to the temperature T raised to the power of 2/3. Our mission is to calculate the work done by the gas when its temperature increases by 90 K.
Let's embark on this mathematical journey and see how calculus helps us unravel the physical reality of the gas.
Analyzing the Setup
We are given the relation:
V=kT2/3
where
k is a constant of proportionality. We are also given the change in temperature,
ΔT=90 K. The work done is expressed as
W=xR, and we need to find the numerical value of
x.
Since the problem mentions "a given mass" without specifying the exact amount, it is a standard convention in such competitive exam problems to assume the number of moles n=1 for the sake of determining the coefficient x.
The Master Equation
In thermodynamics, the work done
W by a gas during expansion or compression is given by the integral of pressure with respect to volume:
W=∫pdV
However, we have a slight roadblock. Our given relation is between volume
V and temperature
T, but our integral involves pressure
p and volume
V. To proceed, we must express pressure in terms of variables we know. Enter the ideal gas law:
pV=nRT
Rearranging this for pressure, we get:
p=VnRT
Substituting this into our work integral gives us:
W=∫VnRTdV
The Calculus Bridge
Our integral now contains three variables: T, V, and dV. To evaluate it, we must transform it into an integral with respect to a single variable. Since we are given the change in temperature ΔT, it makes perfect sense to convert everything into terms of T.
We need to find an expression for
dV in terms of
dT. We do this by differentiating our given volume-temperature relation with respect to
T:
V=kT2/3
Using the power rule of differentiation, we get:
dTdV=k⋅32T32−1
dTdV=32kT−1/3
Multiplying both sides by
dT, we isolate
dV:
dV=32kT−1/3dT
The Elegant Simplification
Now, we substitute our expressions for
V and
dV back into the work integral. This is where the magic happens:
W=∫kT2/3nRT(32kT−1/3)dT
At first glance, this looks like a messy algebraic soup. But let's carefully simplify it. Notice how the constant
k appears in both the numerator and the denominator. It perfectly cancels out! We can also pull the constants
32,
n, and
R outside the integral:
W=32nR∫T2/3T⋅T−1/3dT
Let's combine the powers of T in the numerator. T1⋅T−1/3=T1−1/3=T2/3.
So, the integral becomes:
W=32nR∫T2/3T2/3dT
The
T2/3 terms cancel out completely! We are left with the simplest integral possible:
W=32nR∫1dT
Evaluating this integral from an initial temperature
T1 to a final temperature
T2 yields:
W=32nR[T]T1T2
W=32nR(T2−T1)
Since
T2−T1 is simply the change in temperature
ΔT, we arrive at a beautifully concise formula for the work done in this specific process:
W=32nRΔT
Final Calculation
We have successfully distilled the complex calculus into a simple algebraic formula. Now, we just plug in the given values. Assuming
n=1 mole and using the given
ΔT=90 K:
W=32(1)R(90)
W=2⋅R⋅30
W=60R
The problem states that the work done is
xR. By comparing our result, we can clearly see that:
x=60
The Generalized Insight
This problem reveals a powerful generalized pattern. If a gas undergoes a process where V=kTm, following the exact same calculus steps will show that the work done is always W=m⋅nRΔT. In our case, m=2/3, which immediately gives W=32nRΔT. Recognizing these patterns can save you immense time in competitive exams!