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Internal Energy: First Law, Work, and Heat

Internal energy (U) is a state function representing the total energy of a system. The first law of thermodynamics states ΔU = q + w: energy change equals heat transferred plus work done. For ideal gases, U depends only on temperature: ΔU = nCvΔT.

Concept Fundamentals
ΔU = q + w
First Law
w = -PΔV
Work
ΔU = nCvΔT
Ideal gas
Path independent
State fn
Internal Energy CalculatorCompute ΔU from heat, work, or ideal gas parameters

Why This Chemistry Calculation Matters

Why: Internal energy is fundamental to thermodynamics. The first law governs energy conservation. State functions like U are path-independent; heat and work are not. Understanding ΔU is essential for process analysis and calorimetry.

How: Use ΔU = q + w when heat and work are known. For ideal gases, ΔU = nCvΔT (Cv = 3R/2 monatomic, 5R/2 diatomic). Work at constant pressure: w = -PΔV. Sign convention: q > 0 heat in; w > 0 work on system.

  • Internal energy is a state function—depends only on current state, not path.
  • For ideal gases, isothermal processes have ΔU = 0 (U depends only on T).
  • Adiabatic: q = 0, so ΔU = w; isochoric: w = 0, so ΔU = q.

Sample Examples

Calculation Mode

Process Type

Units

Heat added to system (positive) or removed (negative)
Work done on system (positive) or by system (negative)
Number of significant figures for results

For educational and informational purposes only. Verify with a qualified professional.

🔬 Chemistry Facts

📐

First law: ΔU = q + w (energy conservation).

— IUPAC

⚖️

Work by system at constant P: w = -PΔV.

— NIST

💨

Ideal gas: ΔU = nCvΔT; U independent of P and V.

— Kinetic theory

🌡️

Isothermal ideal gas: ΔU = 0, so q = -w.

— Thermodynamics

📋 Key Takeaways

  • ΔU = q + w | First law: internal energy change from heat and work
  • ΔU = nCvΔT | Ideal gas: U depends only on temperature
  • w = -PΔV | Work at constant pressure
  • Isothermal: ΔU = 0 (ideal gas), q = -w

Did You Know?

⚛️

Internal energy is a state function—path independent.

Source: Thermodynamics

🌡️

For ideal gases, ΔU = 0 in isothermal processes.

Source: Kinetic theory

🔥

Adiabatic: q = 0, so ΔU = w (work only).

Source: First law

📊

Isochoric: w = 0, so ΔU = q (heat only).

Source: Constant volume

⚖️

Cv = (3/2)R monatomic, (5/2)R diatomic.

Source: Equipartition

💨

Joule expansion: free expansion has ΔU = 0 for ideal gas.

Source: Joule experiment

How the Internal Energy Calculator Works

Enter heat (q) and work (w) for first law; or moles, Cv, and ΔT for ideal gas; or P, V₁, V₂ for work calculation.

First Law

ΔU = q + w — heat + work

Ideal Gas

ΔU = nCvΔT — U depends only on T

Expert Tips

Sign Conventions

q > 0: heat in; w > 0: work on system.

Cv Values

Monatomic: 12.5; diatomic: 20.8 J/(mol·K).

Process Type

Select isothermal, adiabatic, isochoric, or isobaric.

Units

Use J or kJ consistently; convert P to Pa.

Process Comparison

ProcessConstraintΔU
IsothermalT constant0 (ideal gas)
Adiabaticq = 0w
IsochoricV constantq
IsobaricP constantq + w

Frequently Asked Questions

What is internal energy?

Total energy in a system: kinetic + potential of molecules. State function.

What is the first law?

ΔU = q + w. Energy change equals heat plus work.

Why ΔU = 0 for isothermal ideal gas?

U depends only on T for ideal gases; T constant ⇒ ΔU = 0.

What is w = -PΔV?

Work done BY system at constant P. Expansion (ΔV > 0) ⇒ w < 0.

When is heat capacity Cv used?

For constant-volume processes. ΔU = nCvΔT for ideal gas.

What is adiabatic?

No heat exchange (q = 0). All energy change from work.

How to find work from P-V?

w = -∫P dV. For constant P: w = -PΔV.

Key Numbers

8.314
R (J/(mol·K))
12.5
Cv monatomic (J/(mol·K))
20.8
Cv diatomic (J/(mol·K))
101325
1 atm (Pa)

📚 Official Sources

⚠️ Disclaimer: This calculator uses thermodynamic equations. For precise work, consult NIST Chemistry WebBook and IUPAC Gold Book.

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