21-Mat-A5 Phase Transformations and Thermal Treatment · May 2017
Nivaar worked solution (AI-drafted; not reviewed by a licensed engineer)
Paper format. National Exams, May 2017 — 10-Met-A5, Mechanical Behaviour and Fracture of Materials. Three hours, closed book, any non-communicating calculator permitted. Eight questions of 20 marks each; the rubric states that five questions constitute a complete paper and that only the first five appearing in the answer book are marked. All eight are answered here, because this set is a study resource rather than an exam script. Several questions ask explicitly for essay-format answers, and the marking scheme rewards clarity and organisation, so the discursive answers below are written as structured prose rather than as note form.
The printed exam header reads 10-Met-A5, Mechanical Behaviour and Fracture of Materials. The paper has no phase-transformation or heat-treatment question in the classical (TTT/CCT diagram, hardenability, tempering-curve) sense; the syllabus actually examined is fracture mechanics and fatigue-crack-growth life, strengthening and toughening of engineering materials, creep and fatigue testing, deformation processing, and elastic–plastic forming behaviour.
Reference texts. The answers below are keyed to the works normally recommended for this syllabus code:
Question text not reproduced: the examination questions are © Engineers and Geoscientists BC. Open the official past paper (linked at the top of this page) to read the question, then follow the worked solution below.
The material chosen here is a 2.25Cr–1Mo low-alloy steel, used for elevated-temperature pressure parts, which is subject to both modes in service.
Creep testing (ASTM E139). A round tensile specimen with threaded or shouldered ends is placed in a lever-arm frame and dead-weight loaded, so that the load stays constant while the specimen extends. It sits inside a three-zone split furnace controlled to within about $\pm 2$ °C, with thermocouples in contact with the gauge length, and is soaked at temperature for long enough to stabilise before loading. Extension is measured on the gauge length itself by a high-temperature extensometer with rods passing out of the furnace to a linear transducer, and strain is logged continuously for the duration of the test — hours for a screening test, tens of thousands of hours for design data. Two variants matter: a true creep test records strain against time and is usually stopped at a defined strain, while a stress-rupture test is run to failure and reports only the rupture life and the elongation. Because the load is constant, the true stress rises as the section necks; a servo-controlled constant-stress test removes that artefact where the mechanism is under study.
Fatigue testing (ASTM E466). A polished specimen — surface finish matters enormously, since fatigue starts at the surface — is cycled at constant amplitude either in rotating bending (the classical R. R. Moore machine, giving fully reversed loading at $R=-1$) or, more usefully for design, in axial load control on a servo-hydraulic frame where the mean stress and the ratio $R = \sigma_{\min}/\sigma_{\max}$ can be set independently. The specimen is cycled at 10–100 Hz until it separates, and the number of cycles is recorded. Since a single test yields one data point, a whole population of specimens is tested at a series of stress amplitudes, with run-outs (typically $10^{7}$ cycles) recorded as arrows. Crack-growth data, by contrast, come from a different test — a pre-cracked compact-tension specimen cycled under load control with the crack length followed by compliance or potential drop (ASTM E647) — and yield the Paris-law constants used in Question 3.
How the two representations differ. The contrast is instructive and is the point of the comparison. One creep test produces an entire curve — strain against time on linear axes for one combination of stress and temperature — and a family of such curves is needed to cover the design space; the number pulled out for design use is the minimum (secondary) creep rate $\dot{\varepsilon}_{\min}$ or the time to 1 per cent strain or to rupture, and those are then cross-plotted against stress on log–log axes or collapsed onto a Larson–Miller parameter $P = T(C + \log t_r)$. One fatigue test, in contrast, produces a single point, and the curve emerges only from a population; the axes are stress amplitude against $\log N$, the scatter is wide (a factor of five in life at a given stress is unremarkable), so the curve is drawn as a mean with a survival probability attached. Creep data are deterministic and time-based; fatigue data are statistical and cycle-based.
The word “toughness” is used for three different quantities, with three different units, and the examiner is asking for all three to be separated cleanly. What they share is that each is an energy, not a stress; what distinguishes them is the volume or area over which that energy is reckoned, and how much of the material takes part.
(i) Toughness in elastic deformation — the modulus of resilience. If the deformation is entirely elastic, the only energy the material can absorb is the recoverable strain energy stored in the stretched bonds. Per unit volume this is the area under the elastic part of the stress–strain curve up to yield,
$$U_r \;=\; \int_0^{\varepsilon_y}\sigma\,\mathrm{d}\varepsilon \;=\; \tfrac{1}{2}\sigma_y\varepsilon_y \;=\; \frac{\sigma_y^{2}}{2E}$$with units of joules per cubic metre (equivalently, pascals). It is the property that matters for a spring: the design goal is to store and return as much energy as possible without permanent set, so a spring material wants a high $\sigma_y$ and a low $E$, which is why hard-drawn spring steel, beryllium copper and fibre-reinforced polymers all appear in leaf and coil springs. Note that resilience says nothing about resistance to failure — it measures energy stored, all of which is given back.
(ii) Toughness in plastic deformation — tensile toughness or the work of fracture. Once the material yields, the energy going into it is largely dissipated rather than stored, and the relevant measure is the total area under the nominal stress–strain curve to fracture,
$$U_T \;=\; \int_0^{\varepsilon_f}\sigma\,\mathrm{d}\varepsilon \;\approx\; \left(\frac{\sigma_y+\sigma_{\text{UTS}}}{2}\right)\varepsilon_f$$again in joules per cubic metre. Because $\varepsilon_f$ can be tens of per cent while $\varepsilon_y$ is a fraction of one per cent, plastic toughness is typically two or three orders of magnitude larger than resilience — it is dominated by ductility, not by strength. This is the quantity a Charpy or Izod impact test estimates (reported as an absorbed energy in joules rather than per unit volume, since the deforming volume is fixed by the specimen), and it is what “tough” means in the everyday engineering sense of a material that gives warning, absorbs a crash, and deforms rather than shattering. It also embodies the classic strength–ductility trade-off: every strengthening mechanism in Question 4 raises $\sigma_y$ and lowers $\varepsilon_f$, so the product passes through a maximum.
(iii) Toughness in fast fracture — fracture toughness. Neither of the first two definitions helps once a sharp crack is present, because then almost all of the material is elastic and only a small process zone at the crack tip does any work. The correct measure is the energy dissipated per unit area of new crack surface, the toughness or critical strain-energy release rate $G_c$, in joules per square metre. Its stress-based equivalent is the critical stress-intensity factor,
$$K \;=\; Y\sigma\sqrt{\pi a}, \qquad K = K_c \ \text{at fracture}, \qquad G_c \;=\; \frac{K_c^{2}}{E'}$$with $E'=E$ in plane stress and $E/(1-\nu^{2})$ in plane strain; $K_c$ has the unusual units MPa m${}^{1/2}$. Under plane-strain constraint the value falls to a geometry-independent minimum, $K_{Ic}$, which is the number quoted as a material property (ASTM E399). This is the toughness that governs the fast, unstable fracture of a cracked structure, and — as Question 3(a) of this paper shows — it also fixes the crack length at which a fatigue crack stops growing stably and runs.