First Law of Thermodynamics

Physics
NEET UG
Version 1Updated 23 Mar 2026

The First Law of Thermodynamics is a fundamental principle in physics, essentially a restatement of the law of conservation of energy applied to thermodynamic systems. It posits that energy cannot be created or destroyed in an isolated system, only transformed from one form to another. Specifically, for a thermodynamic system, the change in its internal energy (DeltaUDelta U) is equal to the heat (QQ

Quick Summary

The First Law of Thermodynamics is a direct application of the principle of conservation of energy to thermodynamic systems. It states that the change in a system's internal energy (DeltaUDelta U) is equal to the heat (QQ) added to the system minus the work (WW) done *by* the system on its surroundings, expressed as DeltaU=QWDelta U = Q - W.

Internal energy (UU) is a state function, depending only on the system's current state (primarily temperature for ideal gases). Heat (QQ) and work (WW) are path functions, representing energy transfer mechanisms.

Crucial sign conventions dictate that QQ is positive for heat absorbed and negative for heat released, while WW is positive for work done by the system (expansion) and negative for work done on the system (compression).

This law helps analyze various thermodynamic processes: isochoric (DeltaU=QVDelta U = Q_V, W=0W=0), isobaric (QP=DeltaU+PDeltaVQ_P = Delta U + PDelta V), isothermal (DeltaU=0Delta U = 0, Q=WQ=W for ideal gases), and adiabatic (DeltaU=WDelta U = -W, Q=0Q=0).

Mayer's relation, CPCV=RC_P - C_V = R, links specific heats for ideal gases. The First Law is fundamental to understanding energy conversion in engines, refrigerators, and all physical and biological systems.

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Key Concepts

Internal Energy (DeltaUDelta U) and Temperature

For an ideal gas, internal energy is directly proportional to its absolute temperature. This is because the…

Work Done in P-V Processes

Work done by a gas during expansion or compression is given by W=PdVW = \int P dV. On a P-V diagram, this…

Mayer's Relation and Ratio of Specific Heats

Mayer's relation, CPCV=RC_P - C_V = R, is a crucial link between the molar specific heat capacities at constant…

  • First LawΔU=QW\Delta U = Q - W (where WW is work done *by* system).
  • Sign ConventionsQ>0Q > 0 (absorbed), Q<0Q < 0 (released); W>0W > 0 (by system), W<0W < 0 (on system).
  • Internal Energy (Ideal Gas)UTU \propto T, so ΔU=0\Delta U = 0 for isothermal processes. ΔU=nCVΔT\Delta U = nC_V\Delta T for any process.
  • Work DoneArea under P-V curve. Wisobaric=PΔVW_{isobaric} = P\Delta V. Wisothermal=nRTln(Vf/Vi)W_{isothermal} = nRT \ln(V_f/V_i).
  • IsochoricW=0    ΔU=QVW=0 \implies \Delta U = Q_V.
  • IsobaricW=PΔV    QP=ΔU+PΔVW=P\Delta V \implies Q_P = \Delta U + P\Delta V.
  • Isothermal (Ideal Gas)ΔU=0    Q=W\Delta U=0 \implies Q=W.
  • AdiabaticQ=0    ΔU=WQ=0 \implies \Delta U = -W. Also PVγ=constantPV^\gamma = \text{constant}, TVγ1=constantTV^{\gamma-1} = \text{constant}.
  • Cyclic ProcessΔU=0    Q=Wnet\Delta U=0 \implies Q=W_{net}.
  • Mayer's RelationCPCV=RC_P - C_V = R.
  • Ratio of Specific Heatsγ=CP/CV\gamma = C_P/C_V. Monatomic: γ=5/3\gamma = 5/3. Diatomic: γ=7/5\gamma = 7/5.

Quickly Understand Work: Q is for Quantity of heat, U is for Unique internal energy, W is for Work done. Remember the equation ΔU=QW\Delta U = Q - W. Think of it as: 'Energy Update equals Quick heat in, minus Work out.' For signs: 'Heat IN is INcrease (positive Q), Work OUT is OUTput (positive W).'

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