Class 11 · Notes

Thermal Properties of Matter— Notes, Formulas & Revision

Complete revision notes and formulas for Thermal Properties of Matter (Class 11). Curated for JEE, NEET, AP Physics, SAT, and CUET. Tap any topic to open the live simulation and full PYQ set.

Linear Expansion

ΔL = L₀αΔT — see metals lengthen with temperature.

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Most solids EXPAND when heated. Linear expansion: ΔL = α·L₀·ΔT, where α is the coefficient of linear expansion (K⁻¹).

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Typical α values: steel ~12×10⁻⁶/K, aluminum ~23×10⁻⁶/K, copper ~17×10⁻⁶/K, glass ~9×10⁻⁶/K, invar ~1×10⁻⁶/K.

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Larger α ⇒ more expansion per unit temperature rise.

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Bimetallic strips: two metals with different α bonded together bend on heating — used in thermostats.

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Railway tracks have gaps between rails to accommodate expansion in summer heat.

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Bridges have expansion joints — accommodate thermal length changes.

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Invar (Fe-Ni alloy) has very low α ⇒ used in precision instruments where dimensional stability matters.

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Thermal expansion arises from anharmonic potential at atomic level — atoms vibrate more on heating and move slightly apart.

Linear expansion

Linear approximation valid for moderate ΔT.

New length

L₀ = original length at reference temperature.

Strain due to expansion

Fractional change in length per unit ΔT.

Thermal stress (constrained)

If body can't expand freely, stress builds up.

α is SMALL (~10⁻⁵ /K) — but at large scales (km bridges) gives meters of expansion.

Heating a metal ring with hole INCREASES the hole size (same fractional expansion as solid).

Bimetallic strips bend toward the metal with LOWER α — used as thermostat switches.

Constrained body cannot expand ⇒ huge thermal stress; can damage bridges, rails.

Linear expansion is FIRST-ORDER in ΔT; valid for moderate ranges. At extreme temperatures, nonlinearity matters.

Invar (α ≈ 1×10⁻⁶/K) is used in pendulum clocks, surveying tapes, anywhere stability matters.

Area Expansion

β ≈ 2α — square sheet expanding in 2D.

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Area expansion: ΔA = β·A₀·ΔT, where β = 2α is the area expansion coefficient.

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Holds for isotropic materials (same α in all directions).

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Twice the linear coefficient because A ∝ L².

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Useful for thin plates, sheet metals, surface areas of objects.

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Hole in a plate: increases in area same as solid plate (β·A·ΔT).

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Differential expansion can warp thin plates if heated asymmetrically.

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Most metals: β ~ 20-50 × 10⁻⁶/K. Glass: ~18 × 10⁻⁶/K.

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Bimetallic plates curl into spherical caps when heated uniformly.

Area expansion

Twice the linear coefficient.

New area

Used for plates and sheets.

Fractional area change

Twice fractional linear change.

β = 2α for ISOTROPIC materials — area expands twice as fast as length (since A = L²).

Hole in a plate behaves like solid plate of same area — both expand at the same rate.

Thin metal plates can warp if heated unevenly (one side expands more).

Bimetallic plate ⇒ spherical curve on uniform heating.

Important for thermometer scales, pressure gauges, scientific instruments.

Differential expansion is a key concern in chip-fabrication and aerospace.

Volume Expansion

γ — liquid level rises in a bulb.

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Volume expansion: ΔV = γ·V₀·ΔT, where γ = 3α is the volume expansion coefficient (for isotropic solids).

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Liquids and gases have their OWN γ — usually much larger than solids.

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γ (water) at 20°C: ~2×10⁻⁴/K. γ (mercury): ~1.8×10⁻⁴/K. γ (air at constant P): 1/273 = 3.66×10⁻³/K.

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Gases follow ideal gas law: V/T = const at constant P ⇒ γ_gas = 1/T ≈ 3.66×10⁻³/K at 273 K.

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Liquid expansion is used in mercury and alcohol thermometers.

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Solid container with liquid: APPARENT expansion of liquid = γ_liquid − γ_container (the difference shows up).

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Anomalous behavior of water: density MAX at 4°C; expands when COOLING from 4°C to 0°C.

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Thermal expansion of pavement and concrete is why expansion joints exist in roads and bridges.

Volume expansion (solid)

For isotropic solid: γ ≈ 3α.

New volume

Linear approximation.

Ideal gas (constant P)

Charles's law: V₂/V₁ = T₂/T₁ at constant P.

Apparent vs real (liquid in container)

What you observe vs. true expansion.

γ = 3α for isotropic solids (volume scales as L³).

Liquids have γ much larger than solids; gases even more (γ ≈ 1/T at constant P).

When measuring liquid expansion in a container, must subtract container's expansion.

Hot air rises because heated air expands and becomes less dense.

Anomalous water: γ NEGATIVE between 0°C and 4°C. Density peaks at 4°C ⇒ lakes freeze top-down.

Real-world: bridges, pipes, and railways must accommodate γ·V·ΔT volumetric changes.

Anomalous Water Expansion

Water density peaks at 4°C — unique behavior.

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Water has ANOMALOUS thermal expansion: density INCREASES as it COOLS from 4°C down to 0°C (volume increases).

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Density MAXIMUM at 4°C: ρ = 1000.0 kg/m³.

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Below 4°C: water EXPANDS as it cools further (negative γ).

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When water freezes at 0°C: volume EXPANDS by ~9% (ice less dense than water).

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Why ice FLOATS on water: ice (ρ ≈ 917 kg/m³) < water (ρ = 1000 kg/m³).

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Lakes freeze TOP-DOWN: dense 4°C water sinks; cold (less dense) water and ice float on top.

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Result: aquatic life survives under ice — bottom water stays at 4°C through winter.

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Origin: hydrogen bonding in water creates open hexagonal structure in ice, denser packing in liquid.

Maximum density of water

Critical reference point.

Density of ice (0°C)

About 8% less than water.

Volume of ice vs water

Volume increases ~9% on freezing.

Fraction of iceberg above water

About 9% above water (90% below).

Most substances: density decreases monotonically with T. Water has a unique maximum at 4°C.

Why lakes don't freeze SOLID: dense 4°C water sinks, ice floats. Marine life survives winter.

Pipe bursts in winter: water expands ~9% on freezing — destructive force inside containers.

Iceberg: only ~10% sticks above water (Titanic was struck by submerged portion).

Anomaly is due to hydrogen bonding — at low T, water molecules form an open, less-dense lattice.

Few other substances (Si, Ge, Ga, Bi) also expand on freezing — but water's effect is most dramatic.

Heat ↔ Temperature

Q = mcΔT — same heat ≠ same ΔT (depends on c).

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HEAT (Q) and TEMPERATURE (T) are different physical quantities.

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TEMPERATURE: average kinetic energy of molecules (a measure, like 'velocity').

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HEAT: energy transferred due to temperature difference (a flow, like 'distance').

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Heat flows SPONTANEOUSLY from hot to cold body — equilibrating temperatures.

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Units: Q in joules (J) or calories (1 cal = 4.184 J). T in Kelvin or Celsius.

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Specific heat capacity c: heat needed per kg per K. Q = m·c·ΔT.

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Water has very high c (~4186 J/kg·K) — that's why oceans moderate climate.

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Heat capacity C = m·c — heat needed to raise the WHOLE body by 1 K.

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Body temperature depends on how heat is shared among DEGREES OF FREEDOM (equipartition theorem).

Heat-temperature relation

Heat needed to change temperature by ΔT.

Heat capacity

Total heat to raise whole body by 1 K.

Specific heat of water

Reference value; very high.

Calorie conversion

Useful for nutritional calorie comparisons.

Heat is ENERGY FLOW; temperature is STATE.

When you say 'this body has heat', it's loose language — bodies have INTERNAL ENERGY, transfer HEAT.

Water's high c means it heats and cools slowly — oceans absorb huge heat without much T change.

Same Q applied to two materials: smaller c ⇒ larger ΔT.

Specific heat depends on the SUBSTANCE; heat capacity depends on AMOUNT plus substance.

Calorie (small c) is energy unit. Calorie (capital C) is 1000 cal — used for food labels.

Calorimetry (Mixing)

T_eq = (m₁T₁ + m₂T₂)/(m₁+m₂) — mix two waters.

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Calorimetry: study of heat transfer between bodies. Used to measure specific heat capacities.

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Principle: when two bodies at different T are placed in thermal contact, heat lost by hot = heat gained by cold (no losses).

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Heat balance: m₁·c₁·(T_hot − T_f) = m₂·c₂·(T_f − T_cold). Solve for T_f or unknown c.

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Calorimeter: container designed to minimize heat losses (insulated double-walled, or vacuum-jacketed).

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Water is commonly used in calorimeters because of its high and well-known c.

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Latent heat: heat required for phase change at constant T (e.g., ice → water).

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Method of mixtures: classic experiment using known reference substance and water.

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Bomb calorimeter measures heat of combustion at constant volume.

Heat lost = heat gained

Energy balance, no losses.

Final temperature

Weighted average by heat capacities.

Heat balance with phase change

Add latent heat term L for melting/vaporization.

Heat lost by hot body = heat gained by cold body (in absence of losses).

Final T is the WEIGHTED average — weighted by m·c (heat capacity).

If amounts of heat are equal, larger m·c side changes T less.

Calorimetry experiments require GOOD INSULATION — otherwise heat leaks to environment.

Phase changes happen at FIXED T — heat goes into the phase transition, not raising T.

Specific heat of an unknown substance can be measured by heat balance with water of known mass and c.

Conduction

dQ/dt = kA·ΔT/L — heat flow in a rod.

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Conduction: heat transfer through a material WITHOUT bulk motion of matter — vibrating molecules and electrons share energy.

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Dominant mechanism in solids, especially metals (free electrons).

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Fourier's law: heat current dQ/dt = −kA·(dT/dx), where k = thermal conductivity (W/m·K).

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Steady-state through a slab: dQ/dt = kA·ΔT/L, where L is thickness.

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Good conductors: metals (Cu: ~400 W/m·K, Ag: ~430, Al: ~240). Poor conductors (insulators): wood, plastic, air.

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Thermal resistance R = L/(kA) — analogous to electrical resistance. Series and parallel rules apply.

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Free electrons in metals carry heat efficiently (Wiedemann-Franz law: k/σ ∝ T).

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Used in: heat sinks, thermos flasks (insulation), thermal grease (improve conduction).

Fourier's law

Heat current proportional to temperature gradient.

Steady-state slab

Across slab of thickness L, area A.

Thermal resistance

Analogous to electrical R = ρL/A.

Slabs in series

Heat passes through each in turn.

Slabs in parallel

Heat splits between paths.

Conduction is dominant in solids (especially metals).

Metals conduct heat well because of free electrons (same reason they conduct electricity).

Wood, glass, air have low k — used as INSULATORS.

Series-parallel rules for thermal resistance — just like electrical circuits.

Wiedemann-Franz law: k/σ ∝ T for metals — direct link between electrical and thermal conduction.

Vacuum has no conduction (or convection) — Thermos flask uses double-walled vacuum to block both.

Thermal Conductivity Compared

Silver vs copper vs wood — see speed of heat flow.

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Thermal conductivity k measures how well a material conducts heat. Units: W/m·K.

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k_metals: Cu ≈ 400, Ag ≈ 430, Al ≈ 240, Fe ≈ 80, Steel ≈ 50.

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k_insulators: glass ≈ 0.8, wood ≈ 0.15, concrete ≈ 1, brick ≈ 0.7.

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k_fluids: water ≈ 0.6, air ≈ 0.025.

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k_air is very small — that's why fluff insulation works (trapped air pockets).

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Wiedemann-Franz law: for metals, k/σ = (π²/3)(k_B/e)²·T — linear relation to electrical conductivity.

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Materials with low k are used as insulators (foam, fiberglass, wood, plastic).

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Materials with high k are used in heat sinks (copper, aluminum).

Fourier's law (rate)

Direct dependence on k.

Wiedemann-Franz law

Universal Lorenz number for metals.

Thermal resistance

Low k ⇒ high R ⇒ good insulator.

k of metals is 100-1000× larger than of insulators.

Air is a poor conductor (k ≈ 0.025 W/m·K). Trapped air = good insulator (foam, double-paned windows).

Diamond has the highest k of any natural material (~2200 W/m·K) — covalent lattice with high phonon transport.

Vacuum has ZERO conduction (no medium).

Why a metal feels cold to touch: high k pulls heat from your skin quickly. Wood feels warm: low k.

Wiedemann-Franz: same electrons carry both heat and current ⇒ linear k-σ relation in metals.

Convection Currents

Natural convection — heated fluid rises, cools, sinks.

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Convection: heat transfer by bulk motion of a FLUID (liquid or gas).

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Natural convection: driven by density differences (hot fluid rises, cold fluid sinks).

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Forced convection: pump or fan moves the fluid.

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Doesn't occur in solids (no bulk fluid motion) or vacuum.

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Examples: boiling water, atmosphere circulation (winds), ocean currents, room heating with radiator.

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Newton's law of cooling: rate of heat loss ∝ (T_body − T_surroundings) — assumes convective cooling.

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Convection coefficient h depends on fluid speed, geometry, fluid properties. Typical: natural air h ~ 5 W/m²·K; forced air h ~ 50; water h ~ 500.

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Rayleigh number determines whether convection occurs vs pure conduction in a fluid layer.

Convective heat transfer rate

h = convection coefficient (W/m²·K), A = area, T_s = surface T, T_∞ = bulk fluid T.

Newton's law of cooling

Body's T approaches T_∞ exponentially: T(t) = T_∞ + (T₀ − T_∞)·e^(−kt).

Rayleigh number

Dimensionless; Ra > ~1700 ⇒ convection starts.

Convection needs a fluid (liquid or gas) — not in solids or vacuum.

Natural convection: hot fluid rises (less dense), cold sinks. Drives Hadley cells in atmosphere.

Forced convection (fan, pump): faster but needs energy input.

Free convection coefficients are LOW (~few W/m²·K). Forced is much higher.

Hot air rises ⇒ heat radiators are placed near the floor; AC vents near the ceiling.

Convection currents drive global weather patterns and ocean circulation.

Radiation (Stefan–Boltzmann)

P = εσAT⁴ — blackbody vs polished surface.

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Radiation: heat transfer by ELECTROMAGNETIC WAVES (mostly infrared at terrestrial T). Doesn't need a medium.

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Stefan-Boltzmann law: power radiated per unit area P/A = εσT⁴, with σ = 5.67×10⁻⁸ W/m²·K⁴ and ε = emissivity (0 ≤ ε ≤ 1).

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Black body: ε = 1, perfect absorber and emitter. Sun is approximately a black body at ~5800 K.

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Net radiative exchange: P_net = εσA(T_body⁴ − T_surroundings⁴).

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Wien's law: λ_max·T = 2.898 × 10⁻³ m·K. Peak wavelength of emitted radiation.

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Sun's peak: λ_max ≈ 500 nm (visible). Human body (310 K): peak ~ 9.4 μm (infrared).

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Radiation is how Earth gets energy from Sun (no medium between). Also how Earth loses heat to space.

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Greenhouse effect: atmosphere absorbs outgoing IR, traps heat ⇒ Earth's surface stays warmer.

Stefan-Boltzmann law

Power radiated by surface area A at temperature T.

Net exchange

Body at T_b in surroundings at T_s.

Wien's displacement law

Peak wavelength shifts inversely with T.

Solar constant

Solar power per m² at Earth's orbit, before atmosphere.

Radiation does NOT need a medium — works through vacuum (unlike conduction & convection).

Power radiated ∝ T⁴ — doubles for only ~19% T increase. Hot objects radiate vastly more.

Wien's law: hotter ⇒ shorter peak wavelength (blue/UV); cooler ⇒ infrared.

Emissivity ε depends on surface: black 1, polished metal 0.05.

Earth would be ~33°C colder without greenhouse effect — water vapor and CO₂ trap IR.

All bodies at T > 0 K emit radiation continuously. We see colors because surfaces absorb/emit selectively.

Newton's Law of Cooling

Exponential decay to ambient temperature.

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Newton's law of cooling: rate of cooling of a hot body in air is proportional to its excess temperature over surroundings.

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dT/dt = −k·(T − T_s), where T_s = surroundings, k = cooling constant.

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Solution: T(t) = T_s + (T₀ − T_s)·e^(−kt) — exponential approach to T_s.

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Valid for SMALL temperature differences (in linear regime).

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For large ΔT, convective/radiative cooling is more strongly nonlinear (radiation ∝ T⁴).

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Cooling constant k depends on size, shape, and surface — larger surfaces cool faster.

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Used in: cooling curves of liquids, forensic temperature analysis (post-mortem time of death).

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Hot soup cools faster in a wide bowl (more surface area) than in a tall cup.

Newton's law of cooling

Cooling rate proportional to excess T.

Solution

Exponential approach to ambient.

Half-cooling time

Time for excess T to drop by half.

Average rate over small ΔT

Approximation when computing finite-time cooling.

Cooling is EXPONENTIAL — never reaches T_s exactly, but asymptotically approaches.

Half the cooling happens in t = ln 2 / k.

Larger surface area ⇒ larger k ⇒ faster cooling. Why coffee in a wide cup cools faster.

Higher initial T ⇒ initial cooling rate larger (proportional to excess T).

Newton's law breaks down for large ΔT (radiation ∝ T⁴ dominates).

Forensic application: estimating time of death by body cooling rate (body's k from anatomy, mass, environment).

Phase Change & Latent Heat

Ice → water → steam: T plateaus during phase change.

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Phase change (transition) occurs at a FIXED temperature for a pure substance (e.g., water melts at 0°C, boils at 100°C at 1 atm).

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Latent heat L: energy absorbed/released per kg during phase change. Q = m·L.

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Two main types: LATENT HEAT OF FUSION (L_f) for melting/freezing; LATENT HEAT OF VAPORIZATION (L_v) for boiling/condensing.

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Water: L_f = 334 kJ/kg, L_v = 2260 kJ/kg.

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During phase change, temperature stays CONSTANT even as heat is added — all energy goes into breaking molecular bonds.

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Sublimation: solid → gas (skipping liquid), e.g., dry ice. Deposition: gas → solid.

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Pressure changes phase-transition temperatures (P-T phase diagram).

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Sweating cools you because evaporation of sweat absorbs L_v from your skin.

Heat for phase change

L in J/kg. No T change during phase transition.

Latent heat of fusion (water)

Energy to melt 1 kg of ice at 0°C.

Latent heat of vaporization (water)

Energy to vaporize 1 kg of water at 100°C.

Total heat (with phase change)

Heat ice → water → steam combines specific and latent heats.

During phase change, T stays CONSTANT — all heat goes to phase transition.

L_v >> L_f for water: vaporization requires ~7× more energy than melting (per kg).

Why does sweating cool you? Sweat evaporation absorbs L_v from your body.

Steam at 100°C burns worse than boiling water at 100°C because of the EXTRA L_v released as it condenses on skin.

Pressure cookers raise boiling T (higher P shifts phase boundary).

Phase diagrams plot P vs T; triple point and critical point are key features.

Thermal Properties of Matter on sciphylab (also known as SciPhy, SciPhy Lab, SciPhy Labs). Free physics revision for Class 11, JEE Mains, JEE Advanced, NEET UG, AP Physics 1/2/C, SAT Subject Physics, and CUET-UG.