Sum to an integral in deriving equipartition theorem

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I'm reading this derivation of the equipartition theorem for ideal gasses:



http://vallance.chem.ox.ac.uk/pdfs/Equipartition.pdf



On the second page, it is mentioned that the partition function as a simple sum,



$$displaystyle Z=sum _ie^-varepsilon _i/kT$$



is not adequate to describe a classical gas as the distribution of energies is not discrete, but continuous. Instead, an integral is needed where



$$e^-varepsilon/kT$$



is integrated over positions and momenta of which energy is a function of. But why is this conversion from a sum to an integral correct?



I can understand why an integral is needed, as the distribution of energies is continuous. But why is it correct to just integrate the exponential function to get the sum? Doesn't the integral give us the area under the curve of the exponential function, that is (speaking perhaps non-rigorously), the sum of the values of the function at different points, multiplied by the differentials $dx$, rather than the simple sum of the values? I've seen this kind of thing done in other places as well, and it bugs me.










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  • An integral is also the limit of an infinite number of infinitesimal terms
    – Wolphram jonny
    1 hour ago














up vote
3
down vote

favorite












I'm reading this derivation of the equipartition theorem for ideal gasses:



http://vallance.chem.ox.ac.uk/pdfs/Equipartition.pdf



On the second page, it is mentioned that the partition function as a simple sum,



$$displaystyle Z=sum _ie^-varepsilon _i/kT$$



is not adequate to describe a classical gas as the distribution of energies is not discrete, but continuous. Instead, an integral is needed where



$$e^-varepsilon/kT$$



is integrated over positions and momenta of which energy is a function of. But why is this conversion from a sum to an integral correct?



I can understand why an integral is needed, as the distribution of energies is continuous. But why is it correct to just integrate the exponential function to get the sum? Doesn't the integral give us the area under the curve of the exponential function, that is (speaking perhaps non-rigorously), the sum of the values of the function at different points, multiplied by the differentials $dx$, rather than the simple sum of the values? I've seen this kind of thing done in other places as well, and it bugs me.










share|cite|improve this question























  • An integral is also the limit of an infinite number of infinitesimal terms
    – Wolphram jonny
    1 hour ago












up vote
3
down vote

favorite









up vote
3
down vote

favorite











I'm reading this derivation of the equipartition theorem for ideal gasses:



http://vallance.chem.ox.ac.uk/pdfs/Equipartition.pdf



On the second page, it is mentioned that the partition function as a simple sum,



$$displaystyle Z=sum _ie^-varepsilon _i/kT$$



is not adequate to describe a classical gas as the distribution of energies is not discrete, but continuous. Instead, an integral is needed where



$$e^-varepsilon/kT$$



is integrated over positions and momenta of which energy is a function of. But why is this conversion from a sum to an integral correct?



I can understand why an integral is needed, as the distribution of energies is continuous. But why is it correct to just integrate the exponential function to get the sum? Doesn't the integral give us the area under the curve of the exponential function, that is (speaking perhaps non-rigorously), the sum of the values of the function at different points, multiplied by the differentials $dx$, rather than the simple sum of the values? I've seen this kind of thing done in other places as well, and it bugs me.










share|cite|improve this question















I'm reading this derivation of the equipartition theorem for ideal gasses:



http://vallance.chem.ox.ac.uk/pdfs/Equipartition.pdf



On the second page, it is mentioned that the partition function as a simple sum,



$$displaystyle Z=sum _ie^-varepsilon _i/kT$$



is not adequate to describe a classical gas as the distribution of energies is not discrete, but continuous. Instead, an integral is needed where



$$e^-varepsilon/kT$$



is integrated over positions and momenta of which energy is a function of. But why is this conversion from a sum to an integral correct?



I can understand why an integral is needed, as the distribution of energies is continuous. But why is it correct to just integrate the exponential function to get the sum? Doesn't the integral give us the area under the curve of the exponential function, that is (speaking perhaps non-rigorously), the sum of the values of the function at different points, multiplied by the differentials $dx$, rather than the simple sum of the values? I've seen this kind of thing done in other places as well, and it bugs me.







statistical-mechanics integration phase-space partition-function






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edited 4 mins ago









Qmechanic♦

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S. Rotos

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  • An integral is also the limit of an infinite number of infinitesimal terms
    – Wolphram jonny
    1 hour ago
















  • An integral is also the limit of an infinite number of infinitesimal terms
    – Wolphram jonny
    1 hour ago















An integral is also the limit of an infinite number of infinitesimal terms
– Wolphram jonny
1 hour ago




An integral is also the limit of an infinite number of infinitesimal terms
– Wolphram jonny
1 hour ago










1 Answer
1






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4
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Whenever a sum goes to an integral in the continuous limit, you need to take account of the issue raised by this question. When in doubt, proceed in two steps, as follows.



  1. First write the sum with an explicit 'delta something' to signify the change in the index being summed over. In the present example:

beginequation
Z = sum_i e^-epsilon_i/kT delta i
endequation



The value of this $delta i$ is 1 in this sum.



  1. Next, replace $delta i$ by the product of a density of something and a change in that something. In the present example, you should ask, "how many states are there per unit range of $x,y,z$ and $p_x, p_y, p_z$? The answer is one state per volume $h^3$ of phase space. The value $delta i = 1$ represents the count in $Z$ increasing by 1 state, so the relationship is

beginequation
delta i = delta x delta y delta z delta p_x delta p_y delta p_z / h^3
endequation



which gives us



beginequation
Z = sum_i e^-epsilon_i/kT delta x delta y delta z delta p_x delta p_y delta p_z / h^3
endequation



Now the continuous limit can be taken:



beginequation
Z = int e^-epsilon_i/kT dx dy dz, dp_x dp_y dp_z / h^3
endequation



where the integral sign is a shorthand for six integrals in this example.



That's it. To repeat: this issue comes up whenever a sum goes to an integral; it is not a special feature of kinetic theory or statistical mechanics. I guess some textbook writers simply assume it as a known aspect of this area of mathematics.






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    1 Answer
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    active

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    1 Answer
    1






    active

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    active

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    up vote
    4
    down vote













    Whenever a sum goes to an integral in the continuous limit, you need to take account of the issue raised by this question. When in doubt, proceed in two steps, as follows.



    1. First write the sum with an explicit 'delta something' to signify the change in the index being summed over. In the present example:

    beginequation
    Z = sum_i e^-epsilon_i/kT delta i
    endequation



    The value of this $delta i$ is 1 in this sum.



    1. Next, replace $delta i$ by the product of a density of something and a change in that something. In the present example, you should ask, "how many states are there per unit range of $x,y,z$ and $p_x, p_y, p_z$? The answer is one state per volume $h^3$ of phase space. The value $delta i = 1$ represents the count in $Z$ increasing by 1 state, so the relationship is

    beginequation
    delta i = delta x delta y delta z delta p_x delta p_y delta p_z / h^3
    endequation



    which gives us



    beginequation
    Z = sum_i e^-epsilon_i/kT delta x delta y delta z delta p_x delta p_y delta p_z / h^3
    endequation



    Now the continuous limit can be taken:



    beginequation
    Z = int e^-epsilon_i/kT dx dy dz, dp_x dp_y dp_z / h^3
    endequation



    where the integral sign is a shorthand for six integrals in this example.



    That's it. To repeat: this issue comes up whenever a sum goes to an integral; it is not a special feature of kinetic theory or statistical mechanics. I guess some textbook writers simply assume it as a known aspect of this area of mathematics.






    share|cite|improve this answer


























      up vote
      4
      down vote













      Whenever a sum goes to an integral in the continuous limit, you need to take account of the issue raised by this question. When in doubt, proceed in two steps, as follows.



      1. First write the sum with an explicit 'delta something' to signify the change in the index being summed over. In the present example:

      beginequation
      Z = sum_i e^-epsilon_i/kT delta i
      endequation



      The value of this $delta i$ is 1 in this sum.



      1. Next, replace $delta i$ by the product of a density of something and a change in that something. In the present example, you should ask, "how many states are there per unit range of $x,y,z$ and $p_x, p_y, p_z$? The answer is one state per volume $h^3$ of phase space. The value $delta i = 1$ represents the count in $Z$ increasing by 1 state, so the relationship is

      beginequation
      delta i = delta x delta y delta z delta p_x delta p_y delta p_z / h^3
      endequation



      which gives us



      beginequation
      Z = sum_i e^-epsilon_i/kT delta x delta y delta z delta p_x delta p_y delta p_z / h^3
      endequation



      Now the continuous limit can be taken:



      beginequation
      Z = int e^-epsilon_i/kT dx dy dz, dp_x dp_y dp_z / h^3
      endequation



      where the integral sign is a shorthand for six integrals in this example.



      That's it. To repeat: this issue comes up whenever a sum goes to an integral; it is not a special feature of kinetic theory or statistical mechanics. I guess some textbook writers simply assume it as a known aspect of this area of mathematics.






      share|cite|improve this answer
























        up vote
        4
        down vote










        up vote
        4
        down vote









        Whenever a sum goes to an integral in the continuous limit, you need to take account of the issue raised by this question. When in doubt, proceed in two steps, as follows.



        1. First write the sum with an explicit 'delta something' to signify the change in the index being summed over. In the present example:

        beginequation
        Z = sum_i e^-epsilon_i/kT delta i
        endequation



        The value of this $delta i$ is 1 in this sum.



        1. Next, replace $delta i$ by the product of a density of something and a change in that something. In the present example, you should ask, "how many states are there per unit range of $x,y,z$ and $p_x, p_y, p_z$? The answer is one state per volume $h^3$ of phase space. The value $delta i = 1$ represents the count in $Z$ increasing by 1 state, so the relationship is

        beginequation
        delta i = delta x delta y delta z delta p_x delta p_y delta p_z / h^3
        endequation



        which gives us



        beginequation
        Z = sum_i e^-epsilon_i/kT delta x delta y delta z delta p_x delta p_y delta p_z / h^3
        endequation



        Now the continuous limit can be taken:



        beginequation
        Z = int e^-epsilon_i/kT dx dy dz, dp_x dp_y dp_z / h^3
        endequation



        where the integral sign is a shorthand for six integrals in this example.



        That's it. To repeat: this issue comes up whenever a sum goes to an integral; it is not a special feature of kinetic theory or statistical mechanics. I guess some textbook writers simply assume it as a known aspect of this area of mathematics.






        share|cite|improve this answer














        Whenever a sum goes to an integral in the continuous limit, you need to take account of the issue raised by this question. When in doubt, proceed in two steps, as follows.



        1. First write the sum with an explicit 'delta something' to signify the change in the index being summed over. In the present example:

        beginequation
        Z = sum_i e^-epsilon_i/kT delta i
        endequation



        The value of this $delta i$ is 1 in this sum.



        1. Next, replace $delta i$ by the product of a density of something and a change in that something. In the present example, you should ask, "how many states are there per unit range of $x,y,z$ and $p_x, p_y, p_z$? The answer is one state per volume $h^3$ of phase space. The value $delta i = 1$ represents the count in $Z$ increasing by 1 state, so the relationship is

        beginequation
        delta i = delta x delta y delta z delta p_x delta p_y delta p_z / h^3
        endequation



        which gives us



        beginequation
        Z = sum_i e^-epsilon_i/kT delta x delta y delta z delta p_x delta p_y delta p_z / h^3
        endequation



        Now the continuous limit can be taken:



        beginequation
        Z = int e^-epsilon_i/kT dx dy dz, dp_x dp_y dp_z / h^3
        endequation



        where the integral sign is a shorthand for six integrals in this example.



        That's it. To repeat: this issue comes up whenever a sum goes to an integral; it is not a special feature of kinetic theory or statistical mechanics. I guess some textbook writers simply assume it as a known aspect of this area of mathematics.







        share|cite|improve this answer














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        edited 26 mins ago

























        answered 38 mins ago









        Andrew Steane

        3396




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