Tutorial: How to Read and Apply TTT and CCT Diagrams in Steel Heat Treatment

Time-Temperature-Transformation (TTT) and Continuous Cooling Transformation (CCT) diagrams are the working tools of the heat treatment metallurgist. They encode, in a single graphical form, the complete transformation kinetics of austenite for a given steel composition: which microstructural phases form, at what temperatures and times they begin and end forming, and how cooling rate determines the final hardness, strength, and toughness of the treated component. This tutorial walks through how these diagrams are constructed, how to read them step by step, and how to apply them to practical heat treatment design, hardenability assessment, and weld procedure qualification.

Key Takeaways

  • A TTT diagram shows isothermal transformation behaviour; a CCT diagram shows continuous cooling transformation behaviour. The CCT is more directly applicable to most industrial heat treatment and welding operations.
  • The C-curve nose shape arises from competing temperature dependences: low driving force near Ae1, low diffusivity near Ms — fastest transformation at the intermediate nose temperature (~550–600°C for plain carbon steel).
  • Alloying elements (Mn, Cr, Mo, Ni, B) shift C-curves to longer times and lower temperatures, reducing the critical cooling rate required for martensite formation and increasing hardenability.
  • To read a CCT diagram: draw the cooling curve on the same T-log(t) axes; each transformation region it enters adds a phase; the final microstructure is read at room temperature from the accumulated phase fractions.
  • The weld HAZ CCT diagram differs from the base metal diagram due to higher austenitising temperature and coarser prior austenite grain size — always use HAZ-specific diagrams for weld microstructure prediction.
  • The martensite start temperature Ms decreases with alloy content; steels with Ms below room temperature develop retained austenite that must be addressed by cryogenic treatment or temper cycling.
TTT Diagram — 0.77%C Eutectoid Steel (Schematic, Ae₁ = 727°C) 0 100 200 300 400 500 600 700 800 900 Temperature (°C) 0.1 1 10 100 1,000 10,000 100,000 Time (seconds, log scale) Ae₁ 727°C Mₐ 220°C Mₑ 60°C Austenite (stable / metastable) Fine Pearlite 600–700°C Coarse Pearlite 700–727°C Upper Bainite 400–550°C Lower Bainite 250–400°C Martensite Mₐ to Mₑ A 100% M B ~M C B+M D P+F E Coarse P Nose ~550°C, ~1s CCR Cooling Curves A: Water quench (~300°C/s) → 100% M B: Oil quench (~50°C/s) → M C: Fast air cool → Bainite + M D: Still air (~5°C/s) → P + F E: Furnace cool → Coarse Pearlite Schematic TTT diagram after Bhadeshia & Honeycombe (Steels, 4th ed.) & Atlas of Continuous Cooling Diagrams. © metallurgyzone.com
Figure 1. Annotated TTT (Time-Temperature-Transformation) diagram for 0.77%C eutectoid steel. Blue curves: pearlite transformation start (Ps) and finish (Pf). Green curves: bainite start (Bs) and finish (Bf). Red lines: martensite start Ms (220°C) and finish Mf (60°C). Five cooling curves A–E demonstrate how different cooling rates produce martensite (A, B), bainite + martensite (C), ferrite + pearlite (D), and coarse pearlite (E). The nose of the pearlite C-curve at ~550°C / ~1 s defines the critical cooling rate. © metallurgyzone.com

What Is a TTT Diagram and How Is It Constructed?

A TTT diagram maps the transformation behaviour of austenite when it is instantaneously quenched from the austenitising temperature to a series of fixed sub-critical temperatures and held isothermally. At each hold temperature, the start and finish of each transformation product (ferrite, pearlite, bainite, martensite) are detected by dilatometry (volume change on transformation), metallography, hardness measurement, or high-resolution in-situ X-ray diffraction. The times at which 1% and 99% transformation occurs define the C-curve start and finish at each temperature.

Construction by Dilatometry

The most common experimental technique for TTT diagram construction is high-speed dilatometry. A cylindrical specimen (typically 3–5 mm diameter, 10–15 mm long) is austenitised in a programmed furnace with inert gas atmosphere, quenched by gas jet to the target isothermal temperature in <1 second, and held while the specimen length is continuously measured by a linear variable differential transducer (LVDT). Austenite-to-product transformations involve volume changes (pearlite and ferrite expand, martensite expands more strongly) that appear as slope changes in the dilatation vs time curve.

The Physical Basis of the C-Curve Shape

The characteristic C-shape of the transformation start curve reflects the competing kinetics of two opposing temperature dependencies:

  • Thermodynamic driving force (ΔG): The chemical free energy difference between austenite and the product phase increases with decreasing temperature below the Ae1 equilibrium temperature. Just below Ae1, ΔG is small and transformation is sluggish even though diffusion is fast.
  • Atomic diffusivity (D): Diffusion of carbon and substitutional alloying atoms follows an Arrhenius relationship and decreases exponentially with temperature. Near Ms, diffusion is so slow that transformation is again sluggish even though the driving force is large.

The nose of the C-curve occurs at the intermediate temperature where the product D × ΔG is maximised — approximately 550–600°C for eutectoid steel and lower in temperature for alloy steels. The transformation rate at the nose defines the critical cooling rate: to avoid any diffusional transformation, the steel must be quenched faster than the rate that passes through the nose.

Nucleation and growth rate (simplified Avrami framework):
  Overall transformation rate ∝ N × G
  where:
    N = nucleation rate (nuclei per unit volume per second)
    G = growth rate (m/s)

  Temperature dependence:
    G ∝ D(T) × ΔG(T)    where D(T) = D₀ exp(−Q/RT) [Arrhenius]
    N ∝ exp(−ΔG*/kT)     where ΔG* = critical nucleation barrier

  At high T (near Ae₁):  ΔG(T) small → slow transformation
  At low T (near Ms):     D(T) small  → slow transformation
  At intermediate T:      product N×G maximised → nose of C-curve

Avrami equation for isothermal transformation fraction X:
  X = 1 − exp(−b × t^n)
  where b and n are temperature-dependent constants
  (n ≈ 3–4 for grain boundary nucleation and growth in 3D)

Reading a TTT Diagram: Step-by-Step Guide

1

Identify the axes and their scales

The vertical axis is temperature (°C or K), spanning from below Mf to above the Ae3 austenitising temperature. The horizontal axis is time in seconds on a logarithmic scale — typically from ~0.1 s to 105 s. The log scale compresses the enormous range of transformation times (from milliseconds for martensite to hours for ferrite in low-carbon steel) onto a readable chart. Never read time values off a TTT diagram without checking whether the scale is linear or logarithmic.

2

Locate the key reference temperatures

Identify the labelled horizontal lines: Ae1 (727°C for eutectoid, lower for hypereutectoid, higher for hypoeutectoid — the eutectoid temperature for the specific composition); Ae3 (upper austenite limit, above which ferrite dissolves into austenite on heating); Acm for hypereutectoid steels (cementite dissolution temperature); Ms (martensite start) and Mf (martensite finish). These lines define the temperature ranges of each phase field.

3

Identify the C-curve pairs for each transformation

Each phase region has a transformation start curve (solid line, typically 1% or 5% transformed) and a finish curve (dashed line, typically 95% or 99% transformed). The curves enclose a region: within this region, transformation is in progress. The pearlite C-curves are typically at higher temperature; bainite C-curves are at lower temperature. In many alloy steels (4140, 4340) the pearlite and bainite C-curves are separated by an “untransformed” gap, while in plain carbon steels they are merged into a single continuous C-curve. A separated bainite bay is significant because it means the steel can be austempered to produce 100% bainite without risk of pearlite formation.

4

Locate the nose of the diagram

The nose is the leftmost point of the transformation start curve — the temperature and time at which transformation begins fastest. For a given steel, the critical cooling rate is approximately equal to the nose temperature divided by the nose time: CCR ≈ (Ae1 − Tnose) / tnose. More precisely, it is the slope of the tangent from the austenitising temperature through the nose point on a T vs linear-time plot — but the nose-time approximation is adequate for most practical purposes.

5

Read the hardness annotations

Most published TTT diagrams annotate hardness values (HRC or HV) at representative isothermal hold temperatures. These represent the hardness of the fully transformed product at each temperature: fine pearlite near the nose gives moderate hardness (~40–45 HRC for eutectoid steel); coarse pearlite at high temperature gives low hardness (~25–30 HRC); lower bainite gives near-martensitic hardness (50–55 HRC); upper bainite gives intermediate hardness (35–45 HRC). As-quenched martensite hardness is read from the Ms to Mf range.

6

Check the austenitising conditions stated on the diagram

Every TTT diagram is specific to the austenitising temperature, hold time, and prior austenite grain size used in the experiment. These are stated in the diagram header or caption. A diagram measured at 900°C austenitising temperature for 0.5 h will differ significantly from one measured at 1100°C, because higher austenitising temperature dissolves more carbides, increases carbon in solution, and causes austenite grain growth — all of which shift C-curves to longer times. If you apply a TTT diagram to a heat treatment cycle with different austenitising conditions, the predictions are approximate only.

The CCT Diagram: Continuous Cooling Transformation

The CCT diagram is constructed by measuring transformation start and finish temperatures as a function of continuous cooling rate, not isothermal hold. It is the more practically applicable diagram because all real industrial heat treatment operations — quenching, controlled air cooling, furnace cooling — and all welding thermal cycles involve continuous cooling rather than isothermal holds.

How the CCT Diagram Differs from the TTT Diagram

The key difference is that during continuous cooling, the steel spends progressively less time at each temperature as it cools. Compared with isothermal holding at the same temperature, the steel has had less opportunity to transform by the time it reaches that temperature. The result is that CCT curves are displaced to longer times and lower temperatures compared with the corresponding TTT curves. A rough empirical rule is that the CCT start curve falls approximately 10–50°C below the corresponding TTT start curve at the same time, but this shift is composition- and temperature-dependent.

Relationship between TTT and CCT (Scheil additivity rule):
  For a continuous cooling path T(t), the fraction transformed is estimated
  by the additive rule (Scheil, 1935):

  ∫₀^t dt' / τ(T(t')) = 1    [transformation start condition]

  where τ(T) is the incubation time at temperature T from the TTT diagram.
  This integral is evaluated numerically by dividing the cooling curve
  into small time steps and summing fractional incubation periods.

  Practical implication:
  — Fast cooling segments spend little time at each T → small contribution
  — Slow cooling through the nose contributes most to the integral
  — If ∫ reaches 1.0, transformation starts regardless of cooling path

CCT construction method:
  1. Measure start/finish temperatures by dilatometry at multiple cooling rates
     (typically 0.05, 0.1, 0.5, 1, 5, 10, 50, 100, 500°C/s)
  2. Plot temperature vs log(time) for each cooling rate
  3. Mark start and finish points from dilatation deviations
  4. Connect start points: CCT start curve
  5. Add cooling rate lines and phase fraction annotations
CCT Comparison: 1040 Plain Carbon vs 4140 Alloy Steel (0.40%C) AISI 1040 (0.40C–0.75Mn) Aust. 870°C, GS ASTM 7 100 200 300 400 500 600 700 800 Temperature (°C) 0.1 1 10 100 1,000 10,000 s Ae₃ 780 Ae₁ 725 Mₐ 350 W M O F+M A F+P γ (Austenite) Ferrite Pearlite Bainite Martensite Nose ~640°C,~2s AISI 4140 (0.40C–1.0Cr–0.20Mo) Aust. 870°C, GS ASTM 7 0.1 1 10 100 1,000 10,000 10⁵ s 100 200 300 400 500 600 700 Ae₃ 790 Ae₁ 730 Mₐ 310°C W M O M! ✅ A B+M F F+P γ Austenite Ferrite Pearlite Bainite Nose ~640°C ~80s Effect of Alloying: Cr + Mo shift C-curves right by ~2 decades (100×) 1040: CCR ~60°C/s (water quench required) | 4140: CCR ~5°C/s (oil quench produces martensite) Schematic after Atlas of CCT Diagrams (Verlag Stahleisen) and Bain & Paxton. © metallurgyzone.com
Figure 2. CCT diagram comparison: 1040 plain carbon steel (left) vs 4140 Cr-Mo alloy steel (right), both at 0.40%C. Alloying with 1.0%Cr and 0.20%Mo shifts all C-curves approximately 100× to longer times, reducing the critical cooling rate from ~60°C/s (water quench essential for martensite in 1040) to ~5°C/s (oil quench sufficient for martensite in 4140). In 1040, an oil quench produces a mixed ferrite + martensite microstructure; in 4140, the same oil quench produces a fully martensitic structure with hardness ~56 HRC. © metallurgyzone.com

How to Overlay a Cooling Curve on a CCT Diagram

The most important practical application of a CCT diagram is predicting the microstructure of a steel component after a specific heat treatment quench. The procedure is to draw the actual cooling curve — temperature versus time — on the same axes as the CCT diagram and read the phase regions it passes through.

Calculating a Continuous Cooling Curve

The cooling rate of a steel component depends on its geometry (thickness, diameter), the thermal properties of the steel, and the heat transfer coefficient of the quench medium. Three simplified models are widely used:

1. Newtonian cooling (thin sections, Bi < 0.1):
   T(t) = T_ambient + (T_initial − T_ambient) × exp(−h×A/(ρ×V×c_p) × t)
   Where: h = heat transfer coefficient (W/m²·K)
          A = surface area (m²), V = volume (m³)
          ρ = density (kg/m³), c_p = specific heat (J/kg·K)
   Valid for: thin sheet, wire, small particles where thermal gradient ≈ 0

2. Approximate cooling rate at surface (thick section):
   T_surface(t) ≈ T_quench + (T_austenitise − T_quench) × erf(x / (2√(α×t)))
   Where: α = thermal diffusivity = λ/(ρ×c_p) ≈ 5×10⁻⁶ m²/s for steel
          x = depth from surface
   Valid for: very thick section, short times

3. Rykalin t8/5 for weld HAZ (most used in practice):
   For 3D cooling (thick plate):
   t8/5 ≈ (6700 − 5×T₀) × Q × [1/(500−T₀)² − 1/(800−T₀)²] / (2π×λ)
   Where: Q = heat input (kJ/mm), T₀ = preheat (°C), λ ≈ 0.04 kJ/mm·s·K

   Typical t8/5 values (Q=1.5 kJ/mm, T₀=25°C):
   ~ 7 seconds → maps to CCR of (800−500)/7 ≈ 43°C/s
   On CCT diagram: draw a cooling line from Ae₃ reaching 500°C at t=7s
   → microstructure read from phase regions traversed

Step-by-Step: Reading the Resulting Microstructure

1

Draw the cooling curve on the CCT axes

Plot T vs t (log scale) on the CCT diagram. For a linear cooling rate CR (°C/s), T = Taustenitise − CR × t. On a log time axis this appears as a curve (not a straight line). For many practical purposes, a straight line on the log-time axes is an adequate approximation if the cooling rate does not change dramatically with temperature.

2

Identify each transformation region the cooling curve enters

Reading from high to low temperature, note each transformation region boundary the cooling curve crosses. Entering a region means that phase begins forming. When the cooling curve exits a region by crossing the finish curve, that transformation is complete. If the cooling curve exits by cooling below Ms before transformation finishes, the remainder transforms to martensite.

3

Read the phase fractions from the diagram annotations

Published CCT diagrams annotate phase fractions at the end of each transformation region, typically as percentages: “F 20% / B 30% / M 50%”. If your cooling curve falls between two annotated curves, interpolate. The sum of all phase fractions must total 100%. The hardness of the resulting mixed microstructure is estimated by linear rule of mixtures: HRCmix ≈ Σ(fi × HRCi).

4

Verify whether Ms is reached and estimate retained austenite

If the cooling curve reaches and passes below Ms, martensite forms athermatically. The fraction of martensite at any temperature T < Ms is given by the Koistinen–Marburger equation: fM = 1 − exp(−0.011 × (Ms − T)). For a room-temperature quench (T = 20°C): fM = 1 − exp(−0.011 × (Ms − 20)). Retained austenite = 1 − fM of the fraction that reached Ms.

Ms Temperature Calculation and Retained Austenite

The martensite start temperature is one of the most critical parameters read from a TTT or CCT diagram. It determines how much of the austenite transforms to martensite during quenching to room temperature, and whether retained austenite is a concern. Several empirical equations have been published; the most widely used are:

Andrews (1965) — most widely used for low-to-medium alloy steels:
  Ms (°C) = 539 − 423×%C − 30.4×%Mn − 17.7×%Ni − 12.1×%Cr − 7.5×%Mo

Barbier (1998) — better for high-alloy steels:
  Ms (°C) = 565 − 600×(1−exp(−0.96×%C)) − 31×%Mn − 13×%Si
             − 10×%Cr − 18×%Ni − 12×%Mo − 8×%W + 30×%Al

Koistinen–Marburger martensite fraction at temperature T:
  f_M(T) = 1 − exp(−0.011 × (Ms − T))     [T < Ms]
  f_M(20°C) = 1 − exp(−0.011 × (Ms − 20))  [room temperature quench]

Retained austenite fraction after quench to room temperature:
  γ_R = 1 − f_M(20°C) = exp(−0.011 × (Ms − 20))

Examples:
  1040 steel (Ms ≈ 350°C): f_M(20°C) = 1−exp(−0.011×330) = 1−0.027 = 97.3%
    → Retained austenite ≈ 2.7% (negligible)

  4340 steel (Ms ≈ 300°C): f_M(20°C) = 1−exp(−0.011×280) = 1−0.046 = 95.4%
    → Retained austenite ≈ 4.6% (small but may affect dimensional stability)

  M2 high-speed steel (Ms ≈ −30°C): f_M(20°C) = 1−exp(−0.011×(−50)) = 1−1.73 → 0%
    → Room temperature quench does NOT transform to martensite
    → Sub-zero treatment (−78°C dry ice, or −196°C LN₂) required
Retained Austenite and Dimensional Instability: Retained austenite in carburised gears, bearing races, and precision tool steels can transform to martensite during service (stress-induced transformation or thermally induced during tempering), causing dimensional change, residual stress reversal, and fatigue crack initiation. For bearing steels (52100) and carburised gears, retained austenite above 10–15% by volume is normally considered excessive and requires sub-zero treatment to convert it to martensite before final tempering.

Effect of Alloying Elements on TTT/CCT Position

Element Typical addition Effect on pearlite C-curve Effect on bainite C-curve Effect on Ms Primary mechanism
Carbon (C) 0.20–0.60% Shifts right; raises nose T slightly Shifts right; lowers bainite range Strongly decreases Increases driving force; slows diffusion; stabilises austenite
Manganese (Mn) 0.5–1.8% Strong rightward shift Moderate rightward shift Decreases (~30°C/%) Slows ferrite nucleation; solid solution hardening of austenite
Chromium (Cr) 0.5–2.0% Strong rightward shift (both pearlite and bainite) Strong rightward shift Decreases (~12°C/%) Stabilises carbides; slows diffusion; forms substitutional alloy carbides
Molybdenum (Mo) 0.15–0.50% Strong rightward shift, especially bainite bay Very strong rightward shift (creates bainite bay) Decreases (~7.5°C/%) Most effective at suppressing bainite; segregates to grain boundaries
Nickel (Ni) 0.5–3.5% Moderate rightward shift Moderate rightward shift Decreases (~18°C/%) Stabilises austenite; reduces stacking fault energy; improves toughness
Silicon (Si) 0.15–0.40% Slight rightward shift Strong effect on bainite: retards cementite formation, enables TRIP/bainite Slight decrease Does not partition to carbides; retards cementite precipitation in bainite
Vanadium (V) 0.05–0.20% Modest rightward shift if in solution Modest effect Slight decrease Strong carbide former; primarily refines grain size; most dissolved at high T
Boron (B) 5–30 ppm Very strong rightward shift of ferrite/pearlite only Little effect on bainite Negligible Segregates to grain boundaries; blocks ferrite nucleation at boundaries; must be in solution (not BN)

CCT Diagrams for Weld HAZ: Why They Differ from Base Metal

The heat-affected zone (HAZ) of a weld undergoes a rapid, non-equilibrium thermal cycle quite unlike a conventional furnace heat treatment. The peak temperature varies with distance from the fusion boundary: from near the melting point at the fusion line to barely above Ac1 at the outer edge of the HAZ. The CCT diagram used to predict HAZ microstructure must therefore reflect the specific austenitising conditions of the HAZ sub-zone being analysed.

CGHAZ vs FGHAZ: Different CCT Diagrams

In the coarse-grained HAZ (CGHAZ), peak temperatures of 1200–1400°C dissolve all carbides and nitrides, eliminate grain boundary pinning particles, and allow rapid austenite grain growth to 100–300 μm. This has two effects on the CCT diagram:

  1. More carbon and alloy in solution: dissolved carbides increase the effective carbon equivalent, shifting C-curves further right and increasing hardenability.
  2. Coarser grain size: fewer grain boundary nucleation sites per unit volume shift C-curves to longer times, further increasing hardenability.

The result is that the CGHAZ is significantly more hardenable than the base metal, meaning a lower cooling rate (longer t8/5) is required before the ferrite/pearlite transformation dominates. At normal heat input levels (0.5–2.0 kJ/mm), the CGHAZ often transforms partially or fully to martensite or lower bainite, explaining why the CGHAZ is typically the hardest and most crack-susceptible region in a weld. The HAZ microstructure article provides detailed treatment of the sub-zone structures, while the hydrogen-induced cracking guide addresses the consequences of hard CGHAZ microstructures in the presence of diffusible hydrogen.

Weld HAZ CCT application — worked example:
  Steel: API 5L X65 pipeline, CE(IIW) = 0.43
  Process: SMAW (η = 0.8), preheat T₀ = 50°C
  Heat input Q = 1.4 kJ/mm

  t8/5 (Rykalin 3D, thick plate):
  t8/5 = (6700 − 5×50) × 1.4 × [1/(500−50)² − 1/(800−50)²] / (2π×0.04)
       = (6700−250) × 1.4 × [1/202500 − 1/562500] / 0.2513
       = 6450 × 1.4 × [4.938×10⁻⁶ − 1.778×10⁻⁶] / 0.2513
       = 9030 × 3.16×10⁻⁶ / 0.2513
       ≈ 9030 × 1.258×10⁻⁵
       ≈ 11.4 seconds

  Average cooling rate from 800→500°C: 300°C / 11.4s = 26°C/s

  On the X65 CGHAZ CCT diagram, CR = 26°C/s:
  → Intersects bainite start at ~500°C
  → Produces predominantly lower bainite + some martensite
  → Expected hardness: ~290–320 HV10 (below 248 HV NACE limit: PASS ✓)

  If preheat reduced to 0°C (T₀ = 0°C), same Q = 1.4 kJ/mm:
  t8/5 recalculates to ~8.5s → CR = 35°C/s
  → More martensite in CGHAZ, hardness ~340–360 HV (EXCEEDS NACE limit ✗)
  → Minimum preheat is justified and required

Practical Applications of TTT and CCT Diagrams

Heat Treatment Process Design

When designing a quench-and-temper heat treatment for a steel component, the CCT diagram tells you the minimum quench severity (cooling rate at the centre of the thickest section) required to achieve the target microstructure. For a target of >90% martensite in the centre of a 50 mm diameter bar, you read from the CCT diagram the minimum cooling rate for martensite formation, calculate the Jominy position that corresponds to that cooling rate, and verify from the Jominy curve that the bar centre reaches adequate hardness. For the Jominy calculation from composition, use the Jominy hardenability calculator.

Austempering and Martempering

TTT diagrams are directly applicable to austempering (isothermal transformation in the bainite region to produce a tough, wear-resistant bainitic structure without distortion) and martempering (interrupted quench to just above Ms, hold for temperature equalisation, then cool to martensite — reducing thermal gradients and distortion). For austempering, the TTT diagram shows the temperature and time window within which the desired bainite forms completely before martensite can form: the window between the bainite start and finish curves at the target temperature.

Weld Preheat and Interpass Temperature Selection

As shown in the worked example above, the CCT diagram combined with the Rykalin t8/5 equation provides the quantitative basis for selecting minimum preheat temperatures. By choosing a preheat that produces a t8/5 placing the cooling curve to the right of the martensite region of the HAZ CCT diagram, the risk of hard martensitic HAZ (and hydrogen-induced cracking) is minimised. The preheat temperature calculator implements this methodology per EN 1011-2.

Normalising and Annealing Temperature Selection

For annealing operations, the CCT diagram confirms what microstructure will form at a specific furnace cooling rate. Full annealing (furnace cooling through the pearlite field) produces coarse lamellar pearlite — maximum softness and machinability. Normalising (still-air cooling) produces a finer pearlite and some ferrite — higher strength than annealed, suitable for most structural applications. The annealing and normalising guide covers the practical heat treatment cycle design for each condition.

Frequently Asked Questions

What is the difference between a TTT diagram and a CCT diagram?
A TTT (Time-Temperature-Transformation) diagram describes the transformation behaviour of austenite held at a fixed (isothermal) temperature after quenching. A CCT (Continuous Cooling Transformation) diagram describes transformation during continuous cooling at various cooling rates, which is how industrial heat treatment and welding thermal cycles actually occur. CCT curves are displaced to longer times and lower temperatures compared with TTT curves because continuous cooling gives less time at each temperature. The CCT diagram is more directly applicable to most industrial applications; the TTT is most useful for austempering, martempering, and understanding transformation kinetics.
Why do the C-curves have their characteristic nose shape?
The C-curve nose arises from competing temperature dependences: just below Ae1, the thermodynamic driving force for transformation is small, so transformation is slow despite adequate diffusion; near Ms, the driving force is large but atomic diffusion is too slow for diffusional products to form quickly. At an intermediate nose temperature (~550–600°C for plain carbon steel), the product of driving force and diffusivity is maximised, giving the fastest transformation rate and the shortest incubation time. The nose temperature and nose time define the critical cooling rate for martensite formation.
How do alloying elements shift the TTT/CCT curves?
Most alloying elements (Mn, Cr, Mo, Ni, Si, V, B) retard the diffusional transformation of austenite to ferrite, pearlite, and bainite, shifting C-curves to longer times and lower temperatures. This widens the window for martensite formation and reduces the critical cooling rate. Carbon increases the driving force but also slows diffusion. Molybdenum and chromium are particularly effective at suppressing bainite. Boron in solid solution at 5–30 ppm selectively poisons grain boundaries against ferrite nucleation, dramatically increasing hardenability at trace additions.
What is the critical cooling rate and how do you read it from a CCT diagram?
The critical cooling rate (CCR) is the minimum cooling rate that produces a fully martensitic microstructure by passing to the left of all transformation start curves. On the CCT diagram, it is the tangential cooling curve that just misses the nose of the transformation start boundary. Faster cooling produces 100% martensite; slower cooling intersects one or more C-curves and produces mixed or fully diffusional microstructures. For plain carbon eutectoid steel (~140°C/s in seawater), and for 4340 alloy steel (~3–5°C/s, enabling martensite in oil quench).
What is the martensite start temperature Ms and how is it calculated?
Ms is the temperature at which the martensitic (diffusionless, shear) transformation begins during rapid cooling. Martensite forms athermatically — a fixed fraction at each temperature below Ms, independent of time. The Andrews (1965) equation gives Ms (°C) = 539 − 423×%C − 30.4×%Mn − 17.7×%Ni − 12.1×%Cr − 7.5×%Mo. Ms decreases with alloy content; steels with Ms below room temperature develop retained austenite after quenching, requiring sub-zero treatment to complete the martensitic transformation.
How do you overlay a cooling curve onto a CCT diagram?
Plot the cooling curve (T vs time, on log time axes) on the CCT diagram. Read each transformation region the cooling curve enters: each intersection with a transformation start curve means that phase begins forming; when the curve exits through the finish curve, that transformation is complete. Phase fractions are read from annotations on the diagram. If the cooling curve reaches Ms before all transformation is complete, the remaining austenite transforms to martensite athermatically. The final hardness is estimated by rule of mixtures from the phase fractions and their hardness values.
Why is the CCT diagram for a weld HAZ different from the base metal?
The CGHAZ is austenitised at 1300–1400°C, dissolving carbides and nitrides that would otherwise pin grain boundaries, and allowing coarsening to 100–300 μm prior austenite grain size. Coarser grains have fewer nucleation sites per unit volume for ferrite and pearlite, shifting C-curves to longer times and increasing hardenability above the base metal level. More alloy is also in solid solution at these high peak temperatures, further shifting the curves. This is why CGHAZ HAZ-specific CCT diagrams (measured at 1350°C austenitising temperature) must be used for weld microstructure prediction rather than the standard base metal diagram.
What are the main practical limitations of TTT and CCT diagrams?
Key limitations: (1) Diagrams are specific to the exact composition and austenitising conditions tested; (2) They represent uniformly austenitised material — real components with segregation or composition gradients behave differently; (3) CCT diagrams are measured on small dilatometry specimens with uniform cooling — actual components have thermal gradients; (4) Carbide dissolution, grain size, and retained phases at the austenitising temperature all affect curves in ways not always stated in published diagrams; (5) Phase fraction and hardness annotations are approximate and may not match actual component measurements due to prior history, macro-segregation, and cooling rate variation through the section thickness.
How are TTT and CCT diagrams used in weld procedure qualification?
In weld procedure qualification, the HAZ CCT diagram is used to predict microstructure as a function of weld heat input and preheat temperature. The cooling rate at the HAZ is calculated from the Rykalin equations as a t8/5 time. This t8/5 is overlaid on the CCT diagram to predict whether the HAZ will contain excessive martensite. If so, preheat temperature is increased (slowing cooling) or heat input raised, until the predicted microstructure falls within acceptable hardness limits (e.g., ≤248 HV10 per NACE MR0175 for sour service). Production weld hardness testing per ISO 9015-1 then verifies the prediction.

Recommended References

Steels: Microstructure and Properties — Bhadeshia & Honeycombe (4th Ed.)
The definitive graduate-level text on steel transformations: rigorous treatment of TTT/CCT diagrams, bainite theory, martensite crystallography, and the effect of alloying on transformation kinetics.
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ASM Handbook Vol. 4A — Steel Heat Treating Fundamentals and Processes
Comprehensive practical reference covering CCT diagram construction and application, austenitising practice, quenching media selection, and residual stress in heat-treated steel components.
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Atlas of CCT Diagrams — Verlag Stahleisen (German Steel Institute)
The most comprehensive collection of experimentally determined CCT diagrams for several hundred steel grades, including weld HAZ diagrams at elevated austenitising temperatures.
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Phase Transformations in Metals and Alloys — Porter, Easterling & Sherif
Rigorous treatment of nucleation theory, Avrami kinetics, TTT construction from first principles, and the thermodynamic and kinetic basis for C-curve shape and alloying effects.
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Further Reading

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