18-Env-A5 Air Quality and Pollution Control Engineering · December 2016
Nivaar worked solution (AI-drafted; not reviewed by a licensed engineer)
04-Env-A5 / 18-Env-A5, Air Quality and Pollution Control Engineering — National Exam, December 2016. 3 hours, open book. Question 1 is compulsory; any other four (4) of Questions 2–7 complete the 100-mark paper (only the first five (5) answers in the work book are marked). All seven Problems are answered below.
Reference texts
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 (i) — baghouse sizing.
Given.
| Quantity | Value |
|---|---|
| Gas flow, $Q$ | 50,000 SCFM = 23.61 m³/s |
| Gas-to-cloth ratio, $u_0$ | 0.7 m/min (= 0.01167 m/s) |
| Inlet dust conc., $c_0$ | 10 g/m³ (= 0.010 kg/m³) |
| Cleaning cycle | reverse-flow, once per hour $\Rightarrow t=1$ h = 3,600 s at max loading |
| Bag size | 10 in dia. × 15 ft, 39.09 ft²/bag = 3.632 m²/bag |
| Dust-cake constants | $K_1=350$ (paired with $u_0$ in m/min), $K_2=9\times10^4$ s⁻¹ (paired with $u_0$ in m/s, $c_0$ in kg/m³, $t$ in s) |
Find. The number of bags required and the overall (maximum) pressure drop across the bags.
Approach. Size the total cloth area from $Q$ and the gas-to-cloth ratio, divide by one bag's area to get the bag count; then evaluate the given two-term pressure-drop model at the end of the 1-hour filtration cycle (worst case, just before cleaning).
| Quantity | Result |
|---|---|
| Total cloth area required | 2,024 m² |
| Number of bags | 558 |
| Pressure drop, clean-cloth term | 245 Pa |
| Pressure drop, dust-cake term | 441 Pa |
| Overall pressure drop | 686 Pa ≈ 2.79 in. H₂O |
[Figure not reproduced: Baghouse process schematic. See the official exam paper or the cited reference text.]
Part (ii) — stack-emission monitoring techniques. Particulate: an in-stack opacity monitor / transmissometer continuously measures light attenuation across the duct as a real-time surrogate for particulate loading, used for continuous compliance demonstration. CO: a non-dispersive infrared (NDIR) analyser extracts a sample and measures infrared absorption at CO's characteristic wavelength — fast, selective and the standard reference method. SOₓ: a pulsed-fluorescence analyser excites SO₂ with UV light and measures the resulting fluorescence intensity, which is proportional to SO₂ concentration — highly sensitive and specific, and is EPA/CCME's reference method for continuous SO₂ monitoring.
Part (iii) — atmospheric behaviour of CO and SO₂. CO is chemically fairly stable in the lower troposphere; it is slowly oxidised to CO₂ primarily by reaction with the hydroxyl radical (OH), giving it an atmospheric residence time on the order of one to a few months, long enough to be transported regionally/hemispherically before removal — it does not readily form secondary particulate or acid deposition. SO₂, by contrast, is reactive: it oxidises in the atmosphere (both gas-phase, via OH, and in cloud droplets) to sulphate ($\text{SO}_4^{2-}$) aerosol and sulphuric acid over a period of hours to a few days, so its residence time is much shorter, but that same reactivity makes it the principal precursor of acid rain and fine secondary sulphate particulate, giving it a more regional (rather than global) impact than CO.