Adiabatic Process Equation (P-V)
PVγ=constant Pressure-volume relationship during an adiabatic process.
applies whenReversible adiabatic process; Ideal gas.
thermodynamicsadiabaticideal_gas
Adiabatic Process Equation (P-T)
P1−γTγ=constant Pressure-temperature relationship during an adiabatic process.
applies whenReversible adiabatic process; Ideal gas.
thermodynamicsadiabaticideal_gasjee-advanced
Adiabatic Process Equation (T-V)
TVγ−1=constant Temperature-volume relationship during an adiabatic process.
applies whenReversible adiabatic process; Ideal gas.
thermodynamicsadiabaticideal_gas
Work Done in Adiabatic Process
W=γ−1P1V1−P2V2=γ−1μR(T1−T2) Work calculated for an ideal gas expanding/compressing adiabatically.
applies whenReversible adiabatic process; Ideal gas.
thermodynamicsadiabaticwork
η=1−T1T2=1−Q1Q2 Maximum possible efficiency for a heat engine operating between two temperatures.
applies whenReversible heat engine.
thermodynamicscarnotefficiencyheat_engine
Carnot Cycle Universal Relation
Q2Q1=T2T1 Ratio of heat exchanges equal to the ratio of absolute temperatures.
applies whenReversible Carnot cycle.
thermodynamicscarnottemperature_scale
Specific Heats in Terms of Degrees of Freedom
Cv=2fR,Cp=(2f+1)R,γ=1+f2 Relating Cv, Cp, and gamma to the degrees of freedom (f) of a gas molecule.
applies whenIdeal gas with f degrees of freedom.
thermodynamicsktgdegrees_of_freedomjee-advanced
Molar specific heat capacity of solids at ordinary temperatures.
applies whenSolid elements at ordinary room temperatures (breaks down at low temperatures).
thermodynamicssolidsspecific_heat
Entropy Change for Ideal Gas
ΔS=μCvln(T1T2)+μRln(V1V2) Formula for the change in entropy between two states of an ideal gas.
applies whenIdeal gas.
thermodynamicsentropyideal_gasjee-advanced
First Law of Thermodynamics
ΔQ=ΔU+ΔW Conservation of energy for a thermodynamic system, relating heat, internal energy, and work.
applies whenApplicable to any thermodynamic process.
thermodynamicsfirst_lawenergy
First Law (Differential Form)
dQ=dU+dW Differential form of the First Law of Thermodynamics.
applies whenApplicable for infinitesimal quasi-static processes.
thermodynamicsfirst_lawdifferentialjee-advanced
γ=CvCp Definition of the adiabatic exponent gamma.
thermodynamicsgammaspecific_heat
S=ΔTΔQ Amount of heat required to raise the temperature of a substance by one unit.
thermodynamicsheat_capacity
Equation of state for an ideal gas.
applies whenIdeal gas limit (low pressure, high temperature).
thermodynamicsideal_gasequation_of_state
Heat Exchange at Constant Pressure
ΔQ=μCpΔT Heat absorbed or released during an isobaric process.
applies whenConstant pressure (Isobaric).
thermodynamicsisobaricheat
Work Done in Isobaric Process
W=P(V2−V1)=μR(T2−T1) Work done by an ideal gas at constant pressure.
applies whenConstant pressure (Isobaric); Ideal Gas.
thermodynamicsisobaricwork
Heat Exchange at Constant Volume
ΔQ=ΔU=μCvΔT Heat absorbed or released during an isochoric process.
applies whenConstant volume (Isochoric).
thermodynamicsisochoricheat
Isothermal Process Equation
PV=constant Pressure-volume relationship during an isothermal process (Boyle's Law).
applies whenConstant temperature (Isothermal); Ideal gas.
thermodynamicsisothermalideal_gas
Work Done in Isothermal Process
W=μRTln(V1V2) Work calculated for an ideal gas expanding/compressing at constant temperature.
applies whenConstant temperature (Isothermal); Ideal gas.
thermodynamicsisothermalwork
Heat required to undergo a phase transition without changing temperature.
applies whenPhase transition at constant temperature.
thermodynamicslatent_heatphase_changejee-advanced
Cp−Cv=R Relationship between molar heat capacity at constant pressure and constant volume.
applies whenIdeal gas.
thermodynamicsideal_gasspecific_heat
γmix=n1Cv1+n2Cv2n1Cp1+n2Cp2 Ratio of specific heats for a non-reacting mixture of ideal gases.
applies whenNon-reacting ideal gas mixture.
thermodynamicsmixturegammajee-advanced
Molar Specific Heat Capacity
C=μΔTΔQ Heat required per mole to raise the temperature by one unit.
thermodynamicsmolar_heatmoles
Work Done During Phase Transition
W=P(Vg−Vl) Expansion work done against atmospheric pressure during boiling/melting.
applies whenConstant pressure phase change.
thermodynamicsphase_changework
Polytropic Process Equation
PVn=constant General process equation governing ideal gases.
applies whenReversible polytropic process (n is constant); Ideal gas.
thermodynamicspolytropicideal_gasjee-advanced
Polytropic Molar Heat Capacity
C=Cv+1−nR Molar heat capacity of a gas undergoing a polytropic process.
applies whenReversible polytropic process; Ideal gas.
thermodynamicspolytropicmolar_heatjee-advanced
Work Done in Polytropic Process
W=n−1P1V1−P2V2=n−1μR(T1−T2) Work done by a gas during a polytropic process.
applies whenReversible polytropic process; Ideal gas.
thermodynamicspolytropicworkjee-advanced
Refrigerator Coefficient of Performance
β=WQ2=T1−T2T2 Efficiency metric for a Carnot refrigerator or heat pump.
applies whenIdeal reversible refrigerator.
thermodynamicsrefrigeratorcopjee-advanced
s=mΔTΔQ Heat required per unit mass to raise the temperature by one unit.
thermodynamicsspecific_heatmass
H=−KAdxdT Fourier's law for the rate of heat conduction.
applies whenSteady state heat flow.
thermodynamicsheat_transferconduction
Volume Expansion Coefficient
αv=3α1 Relation between the coefficient of volume expansion and linear expansion.
applies whenIsotropic solids.
thermodynamicsthermal_expansionsolids
W=∫V1V2PdV Integral formulation for work done during volume expansion/compression.
applies whenReversible (quasi-static) process.
thermodynamicsworkintegration