ADIABATIC PROCESS
Adiabatic reversible work, heat and energy
We know that PVr = constant = K
we know,
Because process is reversible than integration will possible from V1 to V2
PVr = K
P1V1r = K
P2V2r = K
P1 = KV1–r
P2 = KV2–r
P1V1 = RT1
and P2V2 = RT2
Another way to find the work done in adiabatic process.
We know that d∵ = dU – ω
d∵ = 0 because process is adiabatic
dU = ω
⇒ ω = dV = CVdT
and
(B) Adiabatic reversible heat:
d∵ = dU – w
d∵ = 0 for adiabat ic process
(C) Adiabatic reversible energy:
From first law
dq = dU – ω
∵ dq = 0
⇒ 0 = dU– ω
⇒
and
Problem. A gas expands isothermally against a constant external pressure of 1 atm from a volume of 10 dm3 to a volume of 20 dm3. In this process it absorbs 800 J of thermal energy from its surrounding calculate DU for the process in joules (because process is irreversible)
Sol.
W = –P(V2 – V1)
= –1 atm (20 dm3 – 10 dm3) = –10 dm3 atm
∵ R = 8.314 JK–1 mol–1 = 8.02 × 10–2 dm3 atm K–1 mol–1
∴ 1 dm3 atm =
1 dm3 atm = 1.013 × 102 J
Put this value in equation we get
W = – 10 dm3 atm
= – 10 × 1.013 × 102 J = –1013 J
i.e. W = –1013 J
Problem. (a) 2.0 mole of an ideal diatomic gas at 300 K and 0.507 MPa are expanded adiabatically to a final pressure of 0.203 MPa against a constant pressure of 0.101 MPa. Calculate the final temperature, q, w, ΔU & ΔH.
Sol. (a) For an adiabat ic process q = 0
i.e.
CV for a diatomic molecule =
(assuming no contribution for vibration)
Substituting the values, we get
Solving for T2, we get
T2 = 270 K
thus
(270 K -300 K)
= –1247.1 J
= –1247.1 J + 2 mol × 8.314 JK–1 mol–1 (–30 K)
= –1745.9 J
or CP – CV = R
⇒
and
= –1745.9 J
Note
Degree of freedom: There are three types of degree of freedom
(1) Translat ional (2) Rotational (3) Vibrational
⇒ If total no. of atoms are N then no. of degree of freedo m is 3 N.
⇒ For any atom or molecule the degree of freedom for translat ional is three (3).
⇒ For any atom or linear mo lecule the degree o f freedom for is 2 (two) and for non linear it is three (3).
⇒ For any atom or linear mo lecule the degree of freedom for vibrat ional is (3N – 5) and for non linear it is (3N – 6).
⇒ The energy contribution for each degree of freedom is 1/2 KT/molecule or 1/2 RT/mole.
⇒ The vibrational degree of freedo m is affected by temperature and it is 0.2 RT at room temperature and RT at high temperature.
Problem. Calculate CV for Na, Cl2 & SO2?
Sol. Total internal energy (U) for linear mo lecule is:
(at high temperature)
(at room temperature)
Total energy (U) for non linear molecular is:
(at high temperature)
(at room temperature)
We know that
⇒
CV for Na:
CV for Cl2:
(for linear molecule)
= 2.7 RT
CV = 2R
CV for SO2:
for non linear molecule)
= 3.3 RT
CV = 3.3 R
Problem. 20 gm of N2 at 300 K is compressed reversible and adiabatically from 20 dm3 to 10 dm3. Calculate the final temperature, q, w, ΔH & ΔU.
Sol. Amount of
i.e., n = 0.714 mol
T1 = 300 K
V1 = 20 dm3
V2 = 10 dm3
T2 = ?
For adiabatic reversible process:
T1(V1)r-1 = T2 (V2)r -1
⇒
Thus
and for linear molecule
Thus
T1 = 300 K × 1.32 = 396 K
Hence,
= 1424.69 J
ΔH = nCP(T2 - T1)
= 0.714 mol 96 K
= 1994.56 J
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1. What is an adiabatic process? |
2. How does an adiabatic process differ from an isothermal process? |
3. What are degrees of freedom in thermodynamics? |
4. How are degrees of freedom related to the number of particles in a system? |
5. Can an adiabatic process have a change in temperature? |
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