pVTn=−pVT=ln(T−An)+C
and
pVTn=−pVT=−T+τo.VAo
where the sign of T− is accounted for.
pVT=12T+τo.rhr+h
More importantly for the x variable axis,
p=TE=TE=Tn.T−Ao1τo=Tn.TEp
p∝Tn and p∝T−, p∝T+
We plot, 50*x/(x+50)*1/2 for r=50. h is a variable. In the same plot graph of -log(x) and 50*x/(x+50)*1/2-log(x).
And we have the practical Gas Law! What about adding T+ particles?
If T+ is added to a system, we start with,
pTVT=pV+ΔW
that results in,
pVTp=pVT=+Aln(Tn)+C=−ln(T−An)+C
and
pVTp=pVT=T+τo.VAo
in both cases they are the same graphs as when temperature is increased by removing T−. By comparing the sum of the two plots for adding T+ and subtracting T− with practical gas law plots
We have a visual match. This means the two variations are not equivalent at any level. The expression,
p=TE=Tn.TEp={ln(T−An)+C}ηT
is WRONG.
Both processes apply at the same time. How is it possible that Tn changes with T held constant? T is not related to Tn, as yet. It could be that, as the volume AND pressure changes the number of T− particles in the system changes to maintain T, because,
pVTn=pηT
where ηT is the volume density of Tn particles. Changing volume changes the interior surface area and redistributes T−. As area changes pressure changes. The total number of Tn particles changes because pressure changes via,
p=TE=Tn.TEp
The setup that maintains the temperature of the system adds or removes temperature particles.
It is possible that temperature T is related to, the pressure component
pd=TE=Tn.TEp
due to the distribution of Tn on the inner surface of the containment. And not the free (gaseous) component,
pg={ln(T−An)+C}TnV={ln(T−An)+C}ηT
from which negative work was derived.
Have a nice day.