CCE478 - Terminal Effects: Thermodynamics and Chemistry Notes

Units and Conversions

  • Mass, m (g) · Moles, n (mol) · Molar mass, M (g/mol)
    • m = n × M
    • n = m / M
    • M = m / n
  • Converting Between Mass and Moles (summary formulas):
    • m=nMm = n\,M
    • n=mMn = \dfrac{m}{M}
    • M=mnM = \dfrac{m}{n}

SI Units and Prefixes

  • International System of Units (SI) basics
  • SI Base Units:
    • Length: meter, symbol mm
    • Mass: kilogram, symbol kgkg
    • Time: second, symbol ss
    • Temperature: kelvin, symbol KK
    • Amount of substance: mole, symbol molmol
  • Secondary units (examples):
    • Newton, symbol NN
    • Pascal, symbol PaPa
    • Joule, symbol JJ
  • SI prefixes and their factors (examples):
    • tera (T): 101210^{12}
    • giga (G): 10910^{9}
    • mega (M): 10610^{6}
    • kilo (k): 10310^{3}
    • hecto (h): 10210^{2}
    • deka (da): 10110^{1}
    • deci (d): 10110^{-1}
    • centi (c): 10210^{-2}
    • milli (m): 10310^{-3}
    • micro (µ): 10610^{-6}
    • nano (n): 10910^{-9}
    • pico (p): 101210^{-12}
  • SI Derived Units (examples):
    • energy: joule, symbol JJ (also expressed as NmN\cdot m)
    • force: newton, symbol NN
    • pressure: pascal, symbol PaPa
    • power: watt, symbol WW
    • electric charge: coulomb, symbol CC
    • electric potential: volt, symbol VV
    • electric resistance: ohm, symbol Ω\Omega
  • Special note: Unit degree Celsius is equal in magnitude to unit kelvin.

Temperature and Temperature Scales

  • Temperature notions:
    • The centigrade (Celsius) scale was created by Anders Celsius in 1742; widely used.
    • The Kelvin scale is based off Celsius with its 0 point at absolute zero.
  • Temperature scale conversions (from the slide):
    • 373.15K=100C=212F373.15\,\text{K} = 100^{\circ}\text{C} = 212^{\circ}\text{F}
    • 298.15K=25C=77F298.15\,\text{K} = 25^{\circ}\text{C} = 77^{\circ}\text{F}
    • 310.15K=37C=98F310.15\,\text{K} = 37^{\circ}\text{C} = 98^{\circ}\text{F}
    • 273.15K=0C=32F273.15\,\text{K} = 0^{\circ}\text{C} = 32^{\circ}\text{F}
    • 283.15K=10C=50F283.15\,\text{K} = 10^{\circ}\text{C} = 50^{\circ}\text{F}
    • Absolute zero: 273.15C=0K=459.58F-273.15^{\circ}\text{C} = 0\,\text{K} = -459.58^{\circ}\text{F}
    • Room temperature: about 20C68F20^{\circ}\text{C} \approx 68^{\circ}\text{F}
  • On the nano-scale, temperature measures the average speed of molecules; absolute zero corresponds to zero average velocity.

Forms of Energy

  • Forms listed: Heat/Thermal, Potential Energy, Kinetic Energy, Radiant/Light, Electrical, Sound
  • Energy units: Joules (J) as the standard; other common units include ft-lb, BTU, kWh, Calories, electron-volts, etc.
  • The slide notes that energy can be stored in and transferred between these forms; the dimension is that of energy.

Dimensions and Units (SI)

  • Base quantities and symbols:
    • Length: meter, mm
    • Mass: kilogram, kgkg
    • Time: second, ss
    • Temperature: kelvin, KK
    • Amount of substance: mole, molmol
    • Luminous intensity: candela, cdcd
  • SI Derived Units (examples): N(m)N\,(m), PaPa, J(Nm)J\,(N\cdot m), s2s^2, etc. (illustrative from the slide)
  • Prefixes recap (as above).

Chemical Reactions

  • Reactant: a substance that enters into a chemical reaction and is transformed into products (starting material).
  • Product: a substance produced in the course of a chemical reaction (end result).
  • Chemical equations express reactions: reactants → products.

Combustion Reactions

  • Combustion: a reactant (fuel) combines with oxygen to produce simpler products and heat.
  • Example: 2  C<em>4H</em>10+13  O<em>28  CO</em>2+10  H2O+heat2 \;\mathrm{C<em>4H</em>{10}} + 13\; \mathrm{O<em>2} \rightarrow 8\; \mathrm{CO</em>2} + 10\; \mathrm{H_2O} + \text{heat}

Balanced Chemical Equations

  • A chemical equation shows reactants and products; a balanced equation shows the correct stoichiometric ratios.
  • Examples:
    • H<em>2+O</em>2H2O\mathrm{H<em>2} + \mathrm{O</em>2} \rightarrow \mathrm{H_2O}
    • H<em>2+12O</em>2H2O\mathrm{H<em>2} + \tfrac{1}{2}\mathrm{O</em>2} \rightarrow \mathrm{H_2O}
    • 2H<em>2+O</em>22H2O2\mathrm{H<em>2} + \mathrm{O</em>2} \rightarrow 2\mathrm{H_2O}

Balancing Chemical Equations

  • Coefficients are placed in front of reactant/product formulas to balance.
  • Use the smallest possible whole numbers for coefficients (if possible).
  • You cannot change the molecular formulas of the reactants or products to balance.

Systems in Thermodynamics

  • Define a system: the portion of the universe under study.
  • Surroundings: everything outside the system.
  • System types:
    • Isolated: no heat or matter exchange with surroundings
    • Closed: exchange of heat allowed, but no matter exchange
    • Open: exchange of heat and matter allowed
  • The First Law applies to the system and its surroundings, not just the system alone.
  • The transcript shows a condensed energy balance relation for a process, illustrating the partition between system and surroundings.

First Law of Thermodynamics

  • Core idea: energy exists in multiple forms, but total energy of a system and its surroundings is conserved.
  • Axioms described in the transcript:
    • Axiom 1: Internal energy, UU, is an intrinsic property of a system, related to measurable coordinates.
    • Axiom 2: The total energy of the system plus surroundings is conserved.
  • General form (standard thermodynamics): ΔU=QW\Delta U = Q - W where QQ is heat added to the system and WW is work done by the system.
  • Emphasis in the notes is on the role of internal energy and energy exchange with surroundings.

Internal Energy

  • Internal energy arises from molecular motion and interactions:
    • Translational, rotational, and vibrational kinetic energy
    • Potential energy from intermolecular bonds
    • Electronic-nuclear interactions and bond energies that hold atoms/molecules together
  • Internal energy is called internal to distinguish it from kinetic and potential energies with a particular frame of reference.
  • There is no concise standalone thermodynamic definition of internal energy; only changes in U are used in thermodynamics.
  • A linked reference is provided to Crash Course Chemistry for further explanation.

Enthalpy

  • Definition: HU+PVH \equiv U + P V
  • Work for a mechanically reversible, closed-system process: W=PdVW = -\int P\,dV
  • Combining with the energy balance leads to the use of enthalpy as a convenient property, H=U+PVH = U + P V.
  • Constant-volume processes: ΔU=Q\Delta U = Q (since W=0W = 0).
  • Constant-pressure processes: V=ddt(U+PV)=dQdt-V = \dfrac{d}{d t}(U + P V) = \dfrac{dQ}{d t}; equivalently, at constant pressure, ΔH=Q\Delta H = Q.
  • Implication: Enthalpy plays a role at constant pressure analogous to internal energy at constant volume.

Enthalpy and Constant-Pressure Processes (Key Insight)

  • For constant pressure: ΔH=Q\Delta H = Q (heat added at constant pressure).
  • This forms the basis for calorimetry measurements at atmospheric pressure and similar constant-pressure analyses.

Work (Pressure-Volume) and Its Significance

  • Categories of work include:
    • Mechanical work
    • Pressure-Volume (PV) work
    • Rotational work
    • Spring work
    • Non-mechanical work: electric field, electrical polarization, magnetic work, gravitational work
  • PV work formula (classic): W=PdVW = -\int P\,dV
  • PV work describes the work associated with the displacement of a piston in a cylinder, i.e., compression or expansion of a gas.
  • Conditions for PV work to be valid:
    • The system is infinitesimally displaced from a state of internal equilibrium
    • The system is infinitesimally displaced from a state of mechanical equilibrium with its surroundings

Closed Systems (Recap)

  • In a closed system, mass is constant (no transfer of matter across the boundary).
  • All energy exchange with surroundings occurs as heat or work.
  • The total energy change of the surroundings equals the net energy transferred to or from it as heat and work.

Summary: Energy Interconversions and Boundaries

  • The First Law emphasizes energy conservation across system + surroundings.
  • The distinction between constant-volume and constant-pressure processes links Q, W, U, and H in practical ways:
    • Constant volume: ΔU=Q\Delta U = Q (no PV work)
    • Constant pressure: ΔH=Q\Delta H = Q (heat at constant pressure equals enthalpy change)

Real-World Relevance and Connections

  • These concepts underpin energy release in combustion, safety analyses, and lethality assessments where heat transfer, work, and energy storage determine outcomes.
  • The material connects foundational thermodynamics to practical calculations in chemical reactions, engineering systems, and safety assessments.

References in the Transcript

  • Crash Course Chemistry – Enthalpy (video references provided in the transcript):
    • https://www.youtube.com/watch?v=SV7U4yAXL5I&list=PL8dPuuaLjX tPHzzYuWy6fYEaX9mQQ8oGr&index=19
  • Additional practice problems and examples are indicated in the transcript.

Questions?