2013年2月14日木曜日

Internal energy and enthalpy of ideal gas


This is the image which I have.
When I was a freshman at college, and studied entropy.
However, I was not able to understand.
Words did not become a question easily.
I think that there are people with the same question.
And I even forget having had a question.
The next is a clear thing.
I do not understand entropy.

1. Internal Energy of Ideal Gas
The internal energy of n mol ideal gas is expressed as follows.
U=nCvT
Experiment person put n mole ideal gas into the box.
He took care that the size of a box did not change.
He found that energy required to warm 1 was nCv.
This is known as experimental fact.
The theorist explained as follows.
It will be set to nCvT if n mole kinetic energy is all added.

All kinetic energy may be set to 0.
Temperature was set to 0k when kinetic energy was 0.
This is the absolute temperature.
Internal energy is likely to have such a meaning.

Particles in a box collide and rebound upon a stopping wall.
Energy is not given by the wall although particles were perfectly elastic collision.
A box is changed into a piston and compressed.
Particles said.
"Piston’s side is approaching“
Particles get energy from the piston’s side.

The following is an expression of that energy.
nCvdT =-PdV  (1-1)
dV is dV = Sdx.
S is the piston’s area.
dx is the distance.
I think P does not change even if you press only dx.
(1-1) is perhaps the following meanings.
When you press the piston only dx, the temperature was raised only dT.
I think so・・・.

I did the addition of energy in the piston, the kinetic energy of the particles increases our.
I expressed as follows: U internal energy of an ideal gas is increased only dU.
dU = nCvdT =-PdV
I may not know.
What is the necessity to think of P does not change?
Cv is a proportionality constant that does not change the volume.
dV is small, the volume is changed.
I would be using the Cv?
Do not know if I will always think of them.

I cannot be convinced to (1-1).
However, I decided to be convinced that it is right.
(1-1). may be called quasistatic process.
In Japan, it is a freshman at college and learns.
That I learned in first grade college is not always easy.
I was explained as follows.
Quasistatic process takes infinite time.
I thought as follows.
May I be based on such a thing?
Moreover, there are also the following talks.
Quasistatic process does not need time so much.

2Entropy was not changing.

CvT=-PV (1-1)
This is the energy conservation law (1-1).
We have asked the definition of potential temperature equation from this equation.
Japanese meteorologist said.
 "A potential temperature is defined from the law of conservation of energy nCvdT =PdV"
I feel this lacking something.
Consider the ideal gas (T2, P2, V2) and (T1, P1, V1).
Two gases are very similar.
I want the difference between the two gas was like following.
nCv (T1T2) = (P1P2) (V1V2)
If this equation holds, the entropy of (T2, P2, V2) is the same as that (T1, P1, V1).
Someone said I think it reached the definition of entropy.
“On quasistatic process, Entropy does not change.”
(It may be my mistake.)

If nCvdT =PdV, entropy is not changing.
As good as saying that entropy is nCvdT =PdV..
We have described the entropy in entropy.

Entropy is it correct. And Memorize entropy!

I do not know what it is (1-1).
However, nCvdT =-PdV What is the special law of conservation of energy.
Even if it heats the inside of a box with a heater, a principle of conservation of energy is realized (δQ).
It is realized even if it turns a fan in a box (δW).
The principle of conservation of energy is fulfilled also by the following formula.
dU = nCvdT = δQ + δW

nCvdT =PdV is the law of conservation of energy ,and entropy is not changing.
3. Dry Aiabatic lapse rate.
We find the dry adiabatic lapse rate.
Please see the Dry Adiabatic Lapse Rate for more information.
If premised on Hydrostatic equilibrium, there is the following relation.

dP (Z) / P (Z) = (mg / RT (Z)) dz  (3-1)
I do the following with ease.
dP / P = - (mg / RT) dz
Consider the ideal gas of n mole gravitational field.
The state equation is as follows.
P (Z) V (Z) = nRT (Z)
It is as follows if this is differentiated from Z.
dP / P + dV / V = ​​dT / T
The left hand side of (3-1) is now modified as follows.
dP / P = dT / T dV / V
= (dT / T)-PdV / PV
= dT / T-PdV / nRT
Here, We use the (1-1) nCvdT =PdV .

 P/P    =(dT/T)+CvT/RT)  (32)

(3-1) was the following.
 dP/P      -(mg/RT)dz  (31)

It is as follows from (3-1) and (3-2).

(dT/T)+CvT/RT-(mg/RT)dz

We multiplied by RT to both sides.
RTCvT=-mgdZ  (33)
It is Cp = R + Cv from Cp-Cv = R equation of Meyer.
(33) is as follows.
CpT=-mgdZ 

We divide both sides by Cpdz.

T/Z=-mg/Cp (34)

(34) is the dry adiabatic lapse rate.
We will be integral as follows.
CpT+mgZConst (35)

(35) is the law of conservation of energy in something.
Let's define a θ as follows.

CpθCpT+mgZConst  (36)

θ is the value does not change by the Z height.

3Familiar formula of entropy
I asked for the definition of potential temperature equation from the equation of Hydrostatic equilibrium
Hydrostatic equilibrium was that of the following.
dP (Z) / P (Z) = (mg / RT (Z)) dz (3-1)
We integrate both sides.
The integration range of the left side is P (Z) from P0.
P/PlnP(Z)lnP0
From (3-4), the right hand side is the Cp / RdT / T.
The integration range is from T0 to T (Z).
Cp/RT(Z))dz=Cp/R)(lnT(Z)lnT0)

Because it is left-hand side = right side, it looks like this.

lnP(Z)lnP0 Cp/R)(lnT(Z)lnT0)) 
lnP(Z)-(Cp/RlnT(Z)lnP0-(Cp/RlnT0 (42)

Even if Z is any value, lnP(Z)-(Cp/RlnT(Z) is the same value as lnP0-(Cp/RlnT0 which is an initial value.

lnP(Z)-(Cp/RlnT(Z)lnP0-(Cp/RlnT0Const   (43)

An amount that does not change is the entropy of the (43)
.(43) is as follows.
lnP(Z)/P0)=(C/RlnT(Z)/T0) (44)

P0 is set to 1000 and T0 is set to θ.

lnP(Z)/1000)=(C/RlnT(Z)/θ) (45)

(45) defines the potential temperature θ which you know.
This definitional equation has a serious problem.
Please confirm the serious problem by Definition of potential temperature.

5Enthalpy
nCvdT =-PdV (1-1)
I have studied (1-1) in first grade college.
I do not know what that is (1-1) today.
However, it was found that the energy conservation law is entropy does not change (1-1).
The ideal gas, there is a law of conservation of energy that does not change entropy another.
It is the law of conservation of energy using the enthalpy.

It is as follows if the equation of state of ideal gas is differentiated from Z.

VdPPdVnRdT
PVVPnRdT
(31) is as follows.

nCvdT=VPnRdT
nCvdT+nRdT=VdP

Mayer's expression of relations R=Cp-Cv is used.

nCpdT=VdP (51)

(51) was calculated from the following three relations.
They are the Ideal gas law, Mayer's equation, and a principle of conservation of energy (1-1) which does not change entropy.
(51) can be said to be the principle of conservation of energy which does not change entropy.
We can have an image which pushes a piston by (1-1).
However, we cannot have even an image by (5-1).

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