17-Phys-B7 Structure of Materials · May 2013
Nivaar worked solution (AI-drafted; not reviewed by a licensed engineer)
Paper format. 98-Phys-B7 Structure of Materials, National Examination May 2013 — a closed-book examination (Casio or Sharp approved calculators only; all necessary equations, constants and diagrams supplied in the paper's own appendix). Candidates attempt any five of the eight questions, each worth 20 marks; every question is nonetheless answered in full below so the paper remains a complete study resource.
Reference texts. W. D. Callister Jr. & D. G. Rethwisch, Materials Science and Engineering: An Introduction, 10th ed. (atomic bonding, crystal structure and packing, point defects, diffusion, dislocations and slip, mechanical properties, phase diagrams and the lever rule, precipitation hardening, X-ray diffraction); D. J. Griffiths, Introduction to Quantum Mechanics, 3rd ed. (de Broglie wavelength, Heisenberg uncertainty).
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.
Part 1(a). Diffusion flux $J$ is the mass (or number) of atoms crossing a unit cross-sectional area per unit time, $J=\dfrac{M}{At}$ (units $\text{kg}/(\text{m}^2\cdot \text{s})$). Under steady-state conditions it is related to the concentration gradient by Fick's first law, $$J=-D\,\frac{dC}{dx},$$ where $D$ is the diffusion coefficient; the negative sign shows flux runs opposite to (i.e. down) the gradient.
Part 1(b). Diffusion proceeds from regions of high concentration to regions of low concentration — net atomic motion acts to eliminate the concentration gradient and drive the system toward a spatially uniform (minimum free-energy) composition, exactly analogous to heat flowing from hot to cold. The negative sign in Fick's first law encodes this directly: $dC/dx$ is positive in the direction of increasing concentration, so $J=-D\,dC/dx$ must point the opposite way.
Part 1(c). Diffusion rate increases with temperature, because $D$ follows an Arrhenius relation, $$D=D_0\exp\!\left(-\frac{Q_d}{RT}\right),$$ where $Q_d$ is the activation energy for the diffusive jump and $D_0$ a temperature-independent pre-exponential. Raising $T$ increases the fraction of atoms with enough thermal energy to surmount the energy barrier $Q_d$ for a jump into a neighbouring vacant site (or interstitial void), so $D$ — and hence the diffusion rate — rises exponentially with $T$.
Part 2 — Given. $C_s=1.00$ wt%, $C_0=0.20$ wt%, target $C_x= 0.60$ wt% at $x=0.75$ mm; error-function table above.
Find. The carburizing time at 900°C and at 1050°C.
Approach. Use the semi-infinite-solid constant-surface-concentration solution to Fick's second law to get a single target value of $Dt$, then divide by $D(T)$ (Arrhenius) at each temperature.
| Quantity | Value |
|---|---|
| $Z$ (erf argument) | 0.4772 |
| $Dt$ (target) | $6.18\times10^{-7}$ m$^2$ |
| $D$ at 900°C | $5.87\times10^{-12}$ m$^2$/s |
| $D$ at 1050°C | $3.28\times10^{-11}$ m$^2$/s |
| Carburizing time at 900°C | 29.2 h |
| Carburizing time at 1050°C | 5.23 h |