One mole of an ideal gas does 3000 J of work on its surroundings as it expands isothermally to a final pressure of 1.00 atm and volume of 250 L. What is the initial volume and the temperature of the gas?
First, let's note a few important conditions:
- Isothermal means the temperature is held constant, so
#color(green)(DeltaT = 0)# .In these conditions, there is no change in enthalpy
#DeltaH# nor any change in internal energy#DeltaU# . Not sure if we need it, but we should know that#color(blue)(DeltaH = DeltaU = 0)# for an ideal gas if#DeltaT = 0# .- We are given final pressure but not initial pressure, and final volume but not initial volume. So, we would probably have to manipulate the Ideal Gas Law
#PV = nRT# for#T# , and maybe something to do with the work function for#V_1# .REVERSIBLE WORK VS VOLUME
Now, we should know that reversible (efficient) work is defined as:
#\mathbf(w_"rev" = -intPdV)# For this problem, the depiction in a PV-diagram goes like this:
However, since we do not know
#DeltaP# and the equation had assumed that#DeltaP = 0# (note that we are integrating with respect to volume, not pressure), we have use the Ideal Gas Law to rewrite the above equation as:#w_"rev" = -int_(V_1)^(V_2)(nRT)/VdV# Since
#DeltaT = 0# ,#nRT# is a constant. Let's pull it out of the integral.#w_"rev" = -nRTint_(V_1)^(V_2)1/VdV# #= -nRTln|V_2/V_1|# At this point, the shape of the PV-diagram curve looks sensible; it resembles the shape of a
#-lnx# curve.THE INITIAL VOLUME FOR THE EXPANSION
We are given the work, so we should be able to solve for the initial volume,
#V_1# , using this equation. Since expansion work has been done by the gas, meaning that#V_2 > V_1# , we know that#color(green)(w_"rev" < 0)# , numerically.That makes sense because
#ln|V_2/V_1|# when#V_2/V_1 > 1# is positive. Now let's get an expression for#V_1# .#-w_"rev"/(nRT) = ln|V_2/V_1|# #e^(-w_"rev""/"nRT) = V_2/V_1# #e^(w_"rev""/"nRT) = V_1/V_2# #color(green)(V_1 = V_2e^(w_"rev""/"nRT))# However, we do not know the temperature yet, so we'll have to put off calculating the initial volume for a bit longer.
THE TEMPERATURE FOR THE EXPANSION
Something we do know is that the temperature remained constant, so
#T_2 = T_1# . Thus, we have these two relationships that cover the initial and final states:#P_1V_1 = color(blue)(nR)T#
#color(blue)(P_2V_2) = color(blue)(nR)T# We know the values of what is in blue, which is enough.
#color(blue)(T) = (P_2V_2)/(nR) = (("1 atm")("250 L"))/(("1 mol")("0.082057 L"cdot"atm/mol"cdot"K"))# #=# #color(blue)("3046.66 K")# Now we can find the initial volume:
#color(blue)(V_1) = ("250 L")e^((-"3000 J")"/"[("1 mol")("8.314472 J/mol"cdot"K")("3046.66 K")]# #=# #color(blue)("222.08 L")# (As an aside, if you were curious, the initial pressure was about
#"1.126 atm"# , from the Ideal Gas Law.)
- We are given final pressure but not initial pressure, and final volume but not initial volume. So, we would probably have to manipulate the Ideal Gas Law
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The initial volume (( V_i )) and the temperature (( T )) of the gas can be calculated using the ideal gas law and the work done equation for an isothermal process.
Given:
- Work done (( W )) = 3000 J
- Final pressure (( P_f )) = 1.00 atm
- Final volume (( V_f )) = 250 L
Using the ideal gas law ( PV = nRT ), where ( n ) is the number of moles, we can rearrange it to find ( n ): [ n = \frac{PV}{RT} ]
Since the process is isothermal, the temperature (( T )) remains constant. Thus, ( T ) is the same at both initial and final states.
Then, we can find the initial volume (( V_i )) using the work done equation for an isothermal process: [ W = nRT\ln\left(\frac{V_f}{V_i}\right) ]
Rearranging this equation to solve for ( V_i ), we get: [ V_i = V_f \exp\left(-\frac{W}{nRT}\right) ]
Substituting the values and solving for ( V_i ): [ V_i = 250 \times \exp\left(-\frac{3000}{nRT}\right) ]
Once ( V_i ) is found, you can use the ideal gas law to find the temperature ( T ) at either the initial or final state.
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