18-Env-A5 Air Quality and Pollution Control Engineering · May 2016
Nivaar worked solution (AI-drafted; not reviewed by a licensed engineer)
National Exams — May 2016 — 04-Env-A5 / Air Quality and Pollution Control Engineering. 3 hours duration, closed book; Casio or Sharp approved calculator only. Any five (5) questions constitute a complete paper (only the first five answered, as they appear in the workbook, are marked) — all seven Problems are answered in full below as a complete study resource.
Reference texts. Cooper & Alley, Air Pollution Control: A Design Approach (4th ed.); Wark, Warner & Davis, Air Pollution: Its Origin and Control (3rd ed.); Davis & Cornwell, Introduction to Environmental Engineering (6th ed.); Canadian Environmental Protection Act, 1999 (CEPA) and the Canadian Ambient Air Quality Standards (CAAQS) administered by Environment and Climate Change Canada.
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.
Adsorption (e.g. activated-carbon bed). (1) Select an adsorbent with a pore-size distribution and surface area matched to the target VOC molecule, maximizing equilibrium capacity for that species; (2) provide sufficient empty-bed contact time and manage bed regeneration (steam or thermal-swing) so the bed is taken off-line and regenerated before the mass-transfer (adsorption) zone reaches the outlet face and breakthrough occurs, since adsorptive capacity is finite and the bed saturates progressively from the inlet.
Absorption (e.g. packed scrubber tower). (1) Maximize gas–liquid interfacial contact area (packed-bed or spray-tower internals) to enhance the rate of mass transfer of the soluble/reactive pollutant into the liquid phase; (2) select and maintain a scrubbing liquid matched to the pollutant's solubility/reactivity (e.g. water for HCl, a caustic or limestone slurry for SO2) with an adequate liquid-to-gas ratio and countercurrent flow, sustaining the concentration driving force along the full height of the column.
Given. A large-diameter cyclone removing grain dust:
| Quantity | Symbol | Value |
|---|---|---|
| Particle diameters | $d_p$ | 20, 40, 60, 80 µm |
| Inlet width | $B_c$ | 0.5 m |
| Inlet gas velocity | $v_i$ | 30 m/s |
| Particle density | $\rho_p$ | 1300 kg/m³ |
| Gas viscosity | $\mu_g$ | $1.9\times10^{-5}$ kg/(m·s) |
Find. The theoretical cut diameter $[d_p]_{cut}$, and the fractional collection efficiency at each of the four particle sizes from the printed "50% η" curve.
Approach. Compute $[d_p]_{cut}$ directly from the supplied formula, then read the collection efficiency at each of the four given particle sizes off the specified "50% η" curve (the chart's x-axis is the actual particle size, log scale 10–100 µm, not a normalized ratio).
[Figure not reproduced: Cyclone collection efficiency chart, 50% eta curve. See the official exam paper or the cited reference text.]
| Quantity | Value |
|---|---|
| Theoretical cut diameter, $[d_p]_{cut}$ | 18.7 µm |
| Efficiency at $d_p=20\ \mu\text{m}$ | ≈ 4% |
| Efficiency at $d_p=40\ \mu\text{m}$ | ≈ 8% |
| Efficiency at $d_p=60\ \mu\text{m}$ | ≈ 24% |
| Efficiency at $d_p=80\ \mu\text{m}$ | ≈ 70% |
A representative example is a thermal (direct-flame) oxidizer treating solvent-laden exhaust from a printing or coating line: because the VOC-laden air stream is too dilute to support its own flame and too toxic/regulated to vent untreated, raising it to a controlled combustion temperature destroys the organics directly rather than trying to recover them, and applies well where the pollutant is a mix of many different VOCs unsuited to a single adsorbent.
Two key design principles/operating conditions, the first two of the classical "three T's": (1) sufficient temperature (typically 760–870°C for most VOCs) to drive the oxidation reaction to completion; (2) sufficient residence time (typically ≥0.5–1 s) combined with adequate turbulence (mixing) so that every parcel of waste gas actually reaches that temperature for the required dwell time — a chamber whose bulk average temperature is high enough can still under-perform if cold or poorly mixed pockets bypass destruction.
Incineration of waste materials results in: (1) conversion of the organic pollutant primarily to CO2 and H2O, with recoverable thermal energy (often reclaimed via a heat exchanger to preheat the incoming waste stream); (2) any halogenated content converted to acid gases (e.g. HCl from chlorinated solvents), requiring downstream acid-gas scrubbing; (3) a small residual ash/particulate fraction needing further PM control; and, if combustion is incomplete or the flue gas is quenched too quickly through the 200–450°C window, products of incomplete combustion (CO, soot, and in the presence of chlorine, trace dioxins/furans).