Why does there need to be an isothermal compression in a Carnot cycle?












4












$begingroup$


This is the part that allows the Carnot engine to not violate the 2nd law of thermodynamics, but, hypothetically, why can't we just adiabatically compress the working substance to get it back to State A?



As in, the working substance starts at $A$,




  • Isothermal expansion - work is done on the environment

  • Adiabatic expansion - work is done on the environment, temperature is decreasing though so the internal energy of the working substance most now be increased in order for the process to be a cycle

  • Now use an adiabatic compression to bring the internal energy of the working substance back to that of $A$ so that it can repeat the cycle, without rejecting heat to a cold reservoir.


I know it violates the 2nd law of thermodynamics, but is there explanation for as to why this is impossible other than that?










share|cite|improve this question









$endgroup$

















    4












    $begingroup$


    This is the part that allows the Carnot engine to not violate the 2nd law of thermodynamics, but, hypothetically, why can't we just adiabatically compress the working substance to get it back to State A?



    As in, the working substance starts at $A$,




    • Isothermal expansion - work is done on the environment

    • Adiabatic expansion - work is done on the environment, temperature is decreasing though so the internal energy of the working substance most now be increased in order for the process to be a cycle

    • Now use an adiabatic compression to bring the internal energy of the working substance back to that of $A$ so that it can repeat the cycle, without rejecting heat to a cold reservoir.


    I know it violates the 2nd law of thermodynamics, but is there explanation for as to why this is impossible other than that?










    share|cite|improve this question









    $endgroup$















      4












      4








      4


      1



      $begingroup$


      This is the part that allows the Carnot engine to not violate the 2nd law of thermodynamics, but, hypothetically, why can't we just adiabatically compress the working substance to get it back to State A?



      As in, the working substance starts at $A$,




      • Isothermal expansion - work is done on the environment

      • Adiabatic expansion - work is done on the environment, temperature is decreasing though so the internal energy of the working substance most now be increased in order for the process to be a cycle

      • Now use an adiabatic compression to bring the internal energy of the working substance back to that of $A$ so that it can repeat the cycle, without rejecting heat to a cold reservoir.


      I know it violates the 2nd law of thermodynamics, but is there explanation for as to why this is impossible other than that?










      share|cite|improve this question









      $endgroup$




      This is the part that allows the Carnot engine to not violate the 2nd law of thermodynamics, but, hypothetically, why can't we just adiabatically compress the working substance to get it back to State A?



      As in, the working substance starts at $A$,




      • Isothermal expansion - work is done on the environment

      • Adiabatic expansion - work is done on the environment, temperature is decreasing though so the internal energy of the working substance most now be increased in order for the process to be a cycle

      • Now use an adiabatic compression to bring the internal energy of the working substance back to that of $A$ so that it can repeat the cycle, without rejecting heat to a cold reservoir.


      I know it violates the 2nd law of thermodynamics, but is there explanation for as to why this is impossible other than that?







      thermodynamics heat-engine carnot-cycle






      share|cite|improve this question













      share|cite|improve this question











      share|cite|improve this question




      share|cite|improve this question










      asked 15 hours ago









      sangstarsangstar

      1,1251617




      1,1251617






















          2 Answers
          2






          active

          oldest

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          9












          $begingroup$

          Because what you propose is impossible. You are essentially trying to make a cycle out of only these three steps:



          1) Isothermal expansion (A to B)



          2) Adiabatic expansion (B to C)



          3) Adiabatic compression back to original state (C to A)



          The curve going from C to A cannot be an adiabatic process. Adiabatic processes are characterized by
          $$PV^n=text{const}$$
          where $n$ is a property of the gas being used.



          Therefore, if you want to follow an adiabatic curve during compression, you will just end up going back to state B. You can't go to state A from C using an adiabatic compression.



          This is why we need the isothermal compression step after the adiabatic expansion step. This step is needed so that we can get on the correct adiabatic curve back to state A





          To be a little more specific, let's say the pressure and volume at states $B$ and $C$ are $(P_B,V_B)$ and $(P_C,V_C)$ respectively. Then we know in process 2
          $$P_BV_B^n=P_CV_C^n=alpha$$
          Or, in other words, the entire curve is described by $$P=frac{alpha}{V^n}=frac{P_BV_B^n}{V^n}=frac{P_CV_C^n}{V^n}$$
          Now we want to do adiabatic compression from state C. Well we have to follow the curve defined by $PV^n=beta$, but since we know we start in state $C$ it must be that the constant is the same one as before: $beta=alpha=P_CV_C^n$. Therefore, the curve is given by
          $$P=frac{beta}{V^n}=frac{P_CV_C^n}{V^n}$$
          which is the same curve we followed going from B to C.



          We need the isothermal compression step in order to get to the appropriate state D such that $P_DV_D^n=P_AV_A^n$






          share|cite|improve this answer











          $endgroup$













          • $begingroup$
            This is exactly how I would have tackled the problem for ages and ages. But not only is it a mathematical pain-in-the-neck, it is limited by depending on the choice of equation of state. There is a much simpler way ...
            $endgroup$
            – dmckee
            7 hours ago










          • $begingroup$
            @dmckee I guess this is more specific to an ideal gas, but I don't think simple algebra is a pain in the neck. But yeah, it is simpler in the T-S plane here. It seemed like the OP was just learning about this, so I decided to go with what I had initially learned. The T-S plane was introduced to me while studying for the physics GRE, and is a shame that it isn't emphasized more like you say in your answer.
            $endgroup$
            – Aaron Stevens
            5 hours ago



















          3












          $begingroup$

          Examine the problem in the $T$-$S$ plane



          It is traditional for books to diagram the Carnot cycle in the $P$-$V$ plane (it's also useful because the enclosed area is the net work on a cycle).



          It is much less common to diagram it in the $T$-$S$ plane (even though it's just as useful because that enclosed area is the net heat). I suspect that the main reason that diagram is rarely shown explicitly is that it is a boring diagram: it's an axis-aligned rectangle.



          Think about that for a minute.



          If we do one adiabatic stage (vertical movement in the $T$-$S$ plane) and one isothermal stage (horizontal movement), then there is no adiabatic path back to the starting point because adiabatic paths are vertical.



          And this fact is independent of the equation of state of the working fluid: it only relies on the assumption that you are executing adiabatic and isothermal stages.






          share|cite|improve this answer











          $endgroup$













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            2 Answers
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            2 Answers
            2






            active

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            active

            oldest

            votes






            active

            oldest

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            9












            $begingroup$

            Because what you propose is impossible. You are essentially trying to make a cycle out of only these three steps:



            1) Isothermal expansion (A to B)



            2) Adiabatic expansion (B to C)



            3) Adiabatic compression back to original state (C to A)



            The curve going from C to A cannot be an adiabatic process. Adiabatic processes are characterized by
            $$PV^n=text{const}$$
            where $n$ is a property of the gas being used.



            Therefore, if you want to follow an adiabatic curve during compression, you will just end up going back to state B. You can't go to state A from C using an adiabatic compression.



            This is why we need the isothermal compression step after the adiabatic expansion step. This step is needed so that we can get on the correct adiabatic curve back to state A





            To be a little more specific, let's say the pressure and volume at states $B$ and $C$ are $(P_B,V_B)$ and $(P_C,V_C)$ respectively. Then we know in process 2
            $$P_BV_B^n=P_CV_C^n=alpha$$
            Or, in other words, the entire curve is described by $$P=frac{alpha}{V^n}=frac{P_BV_B^n}{V^n}=frac{P_CV_C^n}{V^n}$$
            Now we want to do adiabatic compression from state C. Well we have to follow the curve defined by $PV^n=beta$, but since we know we start in state $C$ it must be that the constant is the same one as before: $beta=alpha=P_CV_C^n$. Therefore, the curve is given by
            $$P=frac{beta}{V^n}=frac{P_CV_C^n}{V^n}$$
            which is the same curve we followed going from B to C.



            We need the isothermal compression step in order to get to the appropriate state D such that $P_DV_D^n=P_AV_A^n$






            share|cite|improve this answer











            $endgroup$













            • $begingroup$
              This is exactly how I would have tackled the problem for ages and ages. But not only is it a mathematical pain-in-the-neck, it is limited by depending on the choice of equation of state. There is a much simpler way ...
              $endgroup$
              – dmckee
              7 hours ago










            • $begingroup$
              @dmckee I guess this is more specific to an ideal gas, but I don't think simple algebra is a pain in the neck. But yeah, it is simpler in the T-S plane here. It seemed like the OP was just learning about this, so I decided to go with what I had initially learned. The T-S plane was introduced to me while studying for the physics GRE, and is a shame that it isn't emphasized more like you say in your answer.
              $endgroup$
              – Aaron Stevens
              5 hours ago
















            9












            $begingroup$

            Because what you propose is impossible. You are essentially trying to make a cycle out of only these three steps:



            1) Isothermal expansion (A to B)



            2) Adiabatic expansion (B to C)



            3) Adiabatic compression back to original state (C to A)



            The curve going from C to A cannot be an adiabatic process. Adiabatic processes are characterized by
            $$PV^n=text{const}$$
            where $n$ is a property of the gas being used.



            Therefore, if you want to follow an adiabatic curve during compression, you will just end up going back to state B. You can't go to state A from C using an adiabatic compression.



            This is why we need the isothermal compression step after the adiabatic expansion step. This step is needed so that we can get on the correct adiabatic curve back to state A





            To be a little more specific, let's say the pressure and volume at states $B$ and $C$ are $(P_B,V_B)$ and $(P_C,V_C)$ respectively. Then we know in process 2
            $$P_BV_B^n=P_CV_C^n=alpha$$
            Or, in other words, the entire curve is described by $$P=frac{alpha}{V^n}=frac{P_BV_B^n}{V^n}=frac{P_CV_C^n}{V^n}$$
            Now we want to do adiabatic compression from state C. Well we have to follow the curve defined by $PV^n=beta$, but since we know we start in state $C$ it must be that the constant is the same one as before: $beta=alpha=P_CV_C^n$. Therefore, the curve is given by
            $$P=frac{beta}{V^n}=frac{P_CV_C^n}{V^n}$$
            which is the same curve we followed going from B to C.



            We need the isothermal compression step in order to get to the appropriate state D such that $P_DV_D^n=P_AV_A^n$






            share|cite|improve this answer











            $endgroup$













            • $begingroup$
              This is exactly how I would have tackled the problem for ages and ages. But not only is it a mathematical pain-in-the-neck, it is limited by depending on the choice of equation of state. There is a much simpler way ...
              $endgroup$
              – dmckee
              7 hours ago










            • $begingroup$
              @dmckee I guess this is more specific to an ideal gas, but I don't think simple algebra is a pain in the neck. But yeah, it is simpler in the T-S plane here. It seemed like the OP was just learning about this, so I decided to go with what I had initially learned. The T-S plane was introduced to me while studying for the physics GRE, and is a shame that it isn't emphasized more like you say in your answer.
              $endgroup$
              – Aaron Stevens
              5 hours ago














            9












            9








            9





            $begingroup$

            Because what you propose is impossible. You are essentially trying to make a cycle out of only these three steps:



            1) Isothermal expansion (A to B)



            2) Adiabatic expansion (B to C)



            3) Adiabatic compression back to original state (C to A)



            The curve going from C to A cannot be an adiabatic process. Adiabatic processes are characterized by
            $$PV^n=text{const}$$
            where $n$ is a property of the gas being used.



            Therefore, if you want to follow an adiabatic curve during compression, you will just end up going back to state B. You can't go to state A from C using an adiabatic compression.



            This is why we need the isothermal compression step after the adiabatic expansion step. This step is needed so that we can get on the correct adiabatic curve back to state A





            To be a little more specific, let's say the pressure and volume at states $B$ and $C$ are $(P_B,V_B)$ and $(P_C,V_C)$ respectively. Then we know in process 2
            $$P_BV_B^n=P_CV_C^n=alpha$$
            Or, in other words, the entire curve is described by $$P=frac{alpha}{V^n}=frac{P_BV_B^n}{V^n}=frac{P_CV_C^n}{V^n}$$
            Now we want to do adiabatic compression from state C. Well we have to follow the curve defined by $PV^n=beta$, but since we know we start in state $C$ it must be that the constant is the same one as before: $beta=alpha=P_CV_C^n$. Therefore, the curve is given by
            $$P=frac{beta}{V^n}=frac{P_CV_C^n}{V^n}$$
            which is the same curve we followed going from B to C.



            We need the isothermal compression step in order to get to the appropriate state D such that $P_DV_D^n=P_AV_A^n$






            share|cite|improve this answer











            $endgroup$



            Because what you propose is impossible. You are essentially trying to make a cycle out of only these three steps:



            1) Isothermal expansion (A to B)



            2) Adiabatic expansion (B to C)



            3) Adiabatic compression back to original state (C to A)



            The curve going from C to A cannot be an adiabatic process. Adiabatic processes are characterized by
            $$PV^n=text{const}$$
            where $n$ is a property of the gas being used.



            Therefore, if you want to follow an adiabatic curve during compression, you will just end up going back to state B. You can't go to state A from C using an adiabatic compression.



            This is why we need the isothermal compression step after the adiabatic expansion step. This step is needed so that we can get on the correct adiabatic curve back to state A





            To be a little more specific, let's say the pressure and volume at states $B$ and $C$ are $(P_B,V_B)$ and $(P_C,V_C)$ respectively. Then we know in process 2
            $$P_BV_B^n=P_CV_C^n=alpha$$
            Or, in other words, the entire curve is described by $$P=frac{alpha}{V^n}=frac{P_BV_B^n}{V^n}=frac{P_CV_C^n}{V^n}$$
            Now we want to do adiabatic compression from state C. Well we have to follow the curve defined by $PV^n=beta$, but since we know we start in state $C$ it must be that the constant is the same one as before: $beta=alpha=P_CV_C^n$. Therefore, the curve is given by
            $$P=frac{beta}{V^n}=frac{P_CV_C^n}{V^n}$$
            which is the same curve we followed going from B to C.



            We need the isothermal compression step in order to get to the appropriate state D such that $P_DV_D^n=P_AV_A^n$







            share|cite|improve this answer














            share|cite|improve this answer



            share|cite|improve this answer








            edited 15 hours ago

























            answered 15 hours ago









            Aaron StevensAaron Stevens

            10.6k31742




            10.6k31742












            • $begingroup$
              This is exactly how I would have tackled the problem for ages and ages. But not only is it a mathematical pain-in-the-neck, it is limited by depending on the choice of equation of state. There is a much simpler way ...
              $endgroup$
              – dmckee
              7 hours ago










            • $begingroup$
              @dmckee I guess this is more specific to an ideal gas, but I don't think simple algebra is a pain in the neck. But yeah, it is simpler in the T-S plane here. It seemed like the OP was just learning about this, so I decided to go with what I had initially learned. The T-S plane was introduced to me while studying for the physics GRE, and is a shame that it isn't emphasized more like you say in your answer.
              $endgroup$
              – Aaron Stevens
              5 hours ago


















            • $begingroup$
              This is exactly how I would have tackled the problem for ages and ages. But not only is it a mathematical pain-in-the-neck, it is limited by depending on the choice of equation of state. There is a much simpler way ...
              $endgroup$
              – dmckee
              7 hours ago










            • $begingroup$
              @dmckee I guess this is more specific to an ideal gas, but I don't think simple algebra is a pain in the neck. But yeah, it is simpler in the T-S plane here. It seemed like the OP was just learning about this, so I decided to go with what I had initially learned. The T-S plane was introduced to me while studying for the physics GRE, and is a shame that it isn't emphasized more like you say in your answer.
              $endgroup$
              – Aaron Stevens
              5 hours ago
















            $begingroup$
            This is exactly how I would have tackled the problem for ages and ages. But not only is it a mathematical pain-in-the-neck, it is limited by depending on the choice of equation of state. There is a much simpler way ...
            $endgroup$
            – dmckee
            7 hours ago




            $begingroup$
            This is exactly how I would have tackled the problem for ages and ages. But not only is it a mathematical pain-in-the-neck, it is limited by depending on the choice of equation of state. There is a much simpler way ...
            $endgroup$
            – dmckee
            7 hours ago












            $begingroup$
            @dmckee I guess this is more specific to an ideal gas, but I don't think simple algebra is a pain in the neck. But yeah, it is simpler in the T-S plane here. It seemed like the OP was just learning about this, so I decided to go with what I had initially learned. The T-S plane was introduced to me while studying for the physics GRE, and is a shame that it isn't emphasized more like you say in your answer.
            $endgroup$
            – Aaron Stevens
            5 hours ago




            $begingroup$
            @dmckee I guess this is more specific to an ideal gas, but I don't think simple algebra is a pain in the neck. But yeah, it is simpler in the T-S plane here. It seemed like the OP was just learning about this, so I decided to go with what I had initially learned. The T-S plane was introduced to me while studying for the physics GRE, and is a shame that it isn't emphasized more like you say in your answer.
            $endgroup$
            – Aaron Stevens
            5 hours ago











            3












            $begingroup$

            Examine the problem in the $T$-$S$ plane



            It is traditional for books to diagram the Carnot cycle in the $P$-$V$ plane (it's also useful because the enclosed area is the net work on a cycle).



            It is much less common to diagram it in the $T$-$S$ plane (even though it's just as useful because that enclosed area is the net heat). I suspect that the main reason that diagram is rarely shown explicitly is that it is a boring diagram: it's an axis-aligned rectangle.



            Think about that for a minute.



            If we do one adiabatic stage (vertical movement in the $T$-$S$ plane) and one isothermal stage (horizontal movement), then there is no adiabatic path back to the starting point because adiabatic paths are vertical.



            And this fact is independent of the equation of state of the working fluid: it only relies on the assumption that you are executing adiabatic and isothermal stages.






            share|cite|improve this answer











            $endgroup$


















              3












              $begingroup$

              Examine the problem in the $T$-$S$ plane



              It is traditional for books to diagram the Carnot cycle in the $P$-$V$ plane (it's also useful because the enclosed area is the net work on a cycle).



              It is much less common to diagram it in the $T$-$S$ plane (even though it's just as useful because that enclosed area is the net heat). I suspect that the main reason that diagram is rarely shown explicitly is that it is a boring diagram: it's an axis-aligned rectangle.



              Think about that for a minute.



              If we do one adiabatic stage (vertical movement in the $T$-$S$ plane) and one isothermal stage (horizontal movement), then there is no adiabatic path back to the starting point because adiabatic paths are vertical.



              And this fact is independent of the equation of state of the working fluid: it only relies on the assumption that you are executing adiabatic and isothermal stages.






              share|cite|improve this answer











              $endgroup$
















                3












                3








                3





                $begingroup$

                Examine the problem in the $T$-$S$ plane



                It is traditional for books to diagram the Carnot cycle in the $P$-$V$ plane (it's also useful because the enclosed area is the net work on a cycle).



                It is much less common to diagram it in the $T$-$S$ plane (even though it's just as useful because that enclosed area is the net heat). I suspect that the main reason that diagram is rarely shown explicitly is that it is a boring diagram: it's an axis-aligned rectangle.



                Think about that for a minute.



                If we do one adiabatic stage (vertical movement in the $T$-$S$ plane) and one isothermal stage (horizontal movement), then there is no adiabatic path back to the starting point because adiabatic paths are vertical.



                And this fact is independent of the equation of state of the working fluid: it only relies on the assumption that you are executing adiabatic and isothermal stages.






                share|cite|improve this answer











                $endgroup$



                Examine the problem in the $T$-$S$ plane



                It is traditional for books to diagram the Carnot cycle in the $P$-$V$ plane (it's also useful because the enclosed area is the net work on a cycle).



                It is much less common to diagram it in the $T$-$S$ plane (even though it's just as useful because that enclosed area is the net heat). I suspect that the main reason that diagram is rarely shown explicitly is that it is a boring diagram: it's an axis-aligned rectangle.



                Think about that for a minute.



                If we do one adiabatic stage (vertical movement in the $T$-$S$ plane) and one isothermal stage (horizontal movement), then there is no adiabatic path back to the starting point because adiabatic paths are vertical.



                And this fact is independent of the equation of state of the working fluid: it only relies on the assumption that you are executing adiabatic and isothermal stages.







                share|cite|improve this answer














                share|cite|improve this answer



                share|cite|improve this answer








                edited 7 hours ago

























                answered 7 hours ago









                dmckeedmckee

                74.4k6134269




                74.4k6134269






























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