17-Phys-B7 Structure of Materials · December 2016
Nivaar worked solution (AI-drafted; not reviewed by a licensed engineer)
Paper format. 98-Phys-B7 Structure of Materials, National Examination December 2016 — a closed-book examination (Casio or Sharp approved calculators only; all necessary equations, constants, the error-function table and the Cu–Ag phase diagram are supplied in the paper's own appendix). Candidates attempt any five of the seven questions, each worth 20 marks; every question is nonetheless answered in full below so the paper remains a complete study resource. This sitting numbers its questions with Roman numerals (Question I–VII) while sub-items inside each question use Arabic numerals (1., 2., 3.).
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, X-ray diffraction); D. J. Griffiths, Introduction to Quantum Mechanics, 3rd ed. (Bohr model, 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 — Given. $E(r)=-\dfrac{A}{r^m}+\dfrac{B}{r^n}$, with $n>m>0$ (the $1/r^m$ term is the long-range attraction, $1/r^n$ the short-range repulsion).
Find. $F(r)$, the equilibrium spacing $r_0$, the maximum binding energy $E(r_0)$, and qualitative $E$–$r$/$F$–$r$ sketches.
Approach. Force is the negative gradient of potential energy, $F=-dE/dr$; equilibrium is where $F=0$; the binding energy is $E$ evaluated at that equilibrium spacing.
Part 2. Dominant bonding type by material:
| Material | Dominant bond type |
|---|---|
| (a) Si | Covalent (diamond-cubic network, $sp^3$ hybrid bonds) |
| (b) Graphite | Covalent in-plane ($sp^2$ hexagonal sheets); weak van der Waals bonding between sheets |
| (c) NaCl | Ionic ($\text{Na}^+/\text{Cl}^-$ electrostatic attraction) |
| (d) SiO$_2$ | Covalent network (Si–O bonds have partial ionic character from the electronegativity difference, but the tetrahedral network is predominantly covalent) |
| (e) Zr | Metallic (delocalized valence electrons, HCP metal) |
Part 3 — Given. $\text{Br}^{-1}$, $Z=35$ (neutral Br), so the anion has $35+1=36$ electrons—the same electron count as krypton.
Find. The four quantum numbers, and one valid set for the valence electron of $\text{Br}^{-1}$.
The four quantum numbers that uniquely specify an electron's state are the principal quantum number $n=1,2,3,\dots$ (principal energy level), the orbital (azimuthal) quantum number $\ell=0,1,\dots,n-1$ (orbital-type shape), the magnetic quantum number $m_\ell=-\ell,\dots,+\ell$ (orbital orientation), and the spin quantum number $m_s=\pm1/2$.
Br ($Z=35$) is $[\text{Ar}]\,3d^{10}\,4s^2\,4p^5$; gaining one electron to form $\text{Br}^{-1}$ fills the $4p$ sub-level completely: $[\text{Ar}]\,3d^{10}\,4s^2\,4p^6$ (isoelectronic with Kr). Every valence electron therefore sits in the full $4p^6$ sub-level, $n=4,\ \ell=1$; one valid combination for a specific electron in that sub-level is $$\boxed{n=4,\ \ell=1,\ m_\ell=0,\ m_s=+\tfrac12}$$ (any of the six $(m_\ell,m_s)$ pairs $m_\ell\in\{-1,0,+1\}$, $m_s=\pm1/2$ is an equally valid answer, since all six $4p$ states are occupied).
| Quantity | Value |
|---|---|
| $F(r)$ | $nB/r^{n+1}-mA/r^{m+1}$ |
| $r_0$ | $(nB/mA)^{1/(n-m)}$ |
| $E(r_0)$ | $-\dfrac{A}{r_0^m}\cdot\dfrac{n-m}{n}$ |
| Si / Graphite / NaCl / SiO$_2$ / Zr bonding | Covalent / covalent+vdW / ionic / covalent(-ionic) / metallic |
| $\text{Br}^{-1}$ valence electron | $n=4,\ell=1,m_\ell=0,m_s=+1/2$ |