23-Chem-A5 Chemical Plant Design and Economics · May 2018
Nivaar worked solution (AI-drafted; not reviewed by a licensed engineer)
Closed-book exam, 3 hours; one aid sheet (both sides) permitted; approved calculator. Six questions of equal value (20 marks each); five constitute a complete paper — full solutions to all six are given here. Question 1 is process synthesis (draw a flowsheet), Question 2 is quantitative (separation-train economics), and Questions 3–6 are design-practice list/essay questions.
Reference texts: M.S. Peters, K.D. Timmerhaus & R.E. West, Plant Design and Economics for Chemical Engineers (5th ed., McGraw-Hill) — the exam's named primary text (process synthesis & flowsheet development Ch. 2–4, general design considerations incl. materials of construction Ch. 3–4, cost & depreciation Ch. 6–9); R. Turton et al., Analysis, Synthesis, and Design of Chemical Processes (4th ed., Prentice Hall) — separation sequencing heuristics and pollution-prevention hierarchy; R.K. Sinnott & G. Towler, Chemical Engineering Design (Coulson & Richardson Vol. 6) — distillation column design and column-internals selection; D.A. Crowl & J.F. Louvar, Chemical Process Safety (4th ed.) — batch-reactor procedures and inherently safer design. Canadian practice framed by CCOHS/WHMIS 2015 and provincial OH&S process-safety expectations.
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.
A complete process design and development package moves from a verified flow scheme to a fully specified, costed and reviewed plant. Ten major items are:
(Two further items often listed — a start-up/operating manual and a waste-treatment/pollution-control design — round out the package.)
Start-up. Confirm the vessel and services are ready: verify the reactor is clean, leak-tight and pressure-tested, that agitator, jacket/coil, relief valve, rupture disc and instrumentation are functional, and that the emergency-cooling and quench systems are armed. Purge with inert gas to remove air where a flammable or oxygen-sensitive charge is involved. Charge the reactants in the specified order and quantity (often the limiting reagent last, added slowly), start the agitator before heating to avoid a local hot-spot, then bring the batch to reaction temperature under controlled heating.
Normal operation. Hold temperature and pressure at set point using the jacket/coil, watching that the cooling capacity always exceeds the reaction's heat-release rate. Control the addition rate of any semi-batch feed so the accumulation of unreacted material — and therefore the potential adiabatic temperature rise — stays bounded. Monitor temperature, pressure, agitation and conversion (sampling or in-line analysis) until the reaction reaches its endpoint.
Shutdown. Stop any feed, cool the batch in a controlled manner, and relieve pressure to a safe location. Transfer the product to downstream hold or work-up, then drain, vent and (if required) wash/purge the reactor. Isolate energy and material sources and return the vessel to a safe, de-energized standby state.
Safety requirements. The governing hazard of a batch reactor is thermal runaway, so the controlling principles are: keep cooling capacity above the maximum heat-release rate; never heat without agitation; limit reagent accumulation (semi-batch dosing interlocked to temperature); provide independent high-temperature/high-pressure trips, emergency cooling or quench (dump/kill), and adequately sized relief to a scrubber or flare; inert flammable atmospheres; and follow permit-to-work, lock-out/tag-out and operator training under the plant's process-safety-management system.