16-Civ-B5 Water Supply and Wastewater Treatment · May 2014
Nivaar worked solution (AI-drafted; not reviewed by a licensed engineer)
Paper format. 98-Civ-B5 Water Supply and Wastewater Engineering, National Examination, May 2014. Three hours; closed book with one aid sheet written on both sides; approved calculator permitted. Question 1 is compulsory and the candidate then attempts any three of Questions 2–5. Every question carries 25 marks, so the paper is marked out of 100. All five questions are solved below — the set is a study resource, not a three-hour sitting.
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.
Given.
| Parameter | Raw water value | Interpretation | Process required |
|---|---|---|---|
| Turbidity | 150–200 NTU | High; a silt-laden surface water, probably a river | Coagulation, flocculation, sedimentation, filtration |
| Total hardness | 300 mg/L as CaCO3 | Very hard | Lime–soda ash softening with recarbonation |
| Iron | 1.0 mg/L | Above the 0.3 mg/L GCDWQ aesthetic objective | Oxidation to Fe(III), then settling and filtration |
| Taste and odour | Seasonal | Algal metabolites (geosmin, MIB) during bloom season | Pre-oxidation plus powdered or granular activated carbon |
| Pathogens | Assumed present (surface source) | Bacteria, viruses, protozoan cysts and oocysts | Filtration credit plus chemical disinfection to a $CT$ target |
Find. A process schematic showing every liquid and solid stream and every chemical injection point, together with the water quality expected after treatment for hardness, turbidity, iron and pathogens.
Approach. The raw water presents four independent problems, and the flowsheet is built by ordering the unit processes so that each one is placed where it does the most work and does not undo another. Oxidation must come first, so that iron is precipitated before the settling step rather than after it. Softening and coagulation are then combined in a single high-pH solids-contact stage, because the same lime that precipitates hardness also assists iron and turbidity removal and produces a heavy, fast-settling floc. Recarbonation follows to bring the pH back down and stabilise the water before filtration, because a supersaturated water would otherwise cement the filter media. Filtration then removes the residual floc, activated carbon polishes taste and odour, and disinfection is placed last, on the clearest water, where the chlorine demand is lowest and the $CT$ credit is cheapest to earn.
| Point | Chemical | Purpose | Typical dose |
|---|---|---|---|
| 1 | Potassium permanganate or chlorine | Pre-oxidation of Fe(II) to insoluble Fe(III); partial destruction of taste-and-odour compounds; algae control | 0.64 mg/L Cl2 or 0.94 mg/L KMnO4 per mg/L Fe |
| 2 | Hydrated lime, Ca(OH)2 | Raises pH to 10.3–11.0 and precipitates carbonate hardness as CaCO3 and magnesium as Mg(OH)2 | 150–250 mg/L, set by a jar test |
| 3 | Soda ash, Na2CO3 | Supplies carbonate to precipitate the non-carbonate fraction of the hardness | as required by the carbonate/non-carbonate split |
| 4 | Ferric sulphate or alum coagulant | Destabilises the 150–200 NTU clay and silt turbidity so it can be flocculated | 20–40 mg/L |
| 5 | Powdered activated carbon (seasonal) and anionic polymer | PAC adsorbs geosmin and MIB during bloom season; polymer strengthens the floc | PAC 5–20 mg/L seasonally; polymer 0.1–0.5 mg/L |
| 6 | Carbon dioxide | Recarbonation: lowers pH from about 10.5 to 8.5–9.0 and converts residual carbonate to bicarbonate so the water does not deposit scale on the filters and mains | to the stabilisation target |
| 7 | Chlorine (primary disinfection) | Inactivation credit earned in the baffled contact tank against the $CT$ target | 1.5–3.0 mg/L to hold the design residual |
| 8 | Ammonia | Converts the free residual to monochloramine for a stable distribution residual and lower THM formation | Cl2:N of 4:1 to 5:1 |
| 9 | Fluoride (where the community fluoridates) | Dental-caries prevention to the Health Canada optimum | to 0.7 mg/L |
| 10 | Orthophosphate or polyphosphate corrosion inhibitor | Forms a passivating film in the distribution system; important after softening, which leaves a less-buffered water | 0.5–1.0 mg/L as PO4 |
The liquid train runs intake and bar screens, rapid mix with pre-oxidation and chemical addition, tapered three-stage flocculation, the solids-contact softener-clarifier, recarbonation, dual-media filtration, granular activated carbon adsorbers, the baffled chlorine contact tank, the clearwell and high-lift pumps, and finally the distribution system. The solids train collects two waste streams: the softening and coagulation sludge drawn continuously from the clarifier floor, which is by far the larger, and the spent backwash water from the filters, which is intermittent and dilute and is therefore equalised before it joins the thickener. Thickened sludge is dewatered mechanically and the cake goes to agricultural land application, where its calcium carbonate content has liming value, or to landfill. The recycle stream returns thickener supernatant, centrifuge centrate and equalised backwash water to the head of the plant; it must be returned at a controlled, steady rate rather than in slugs, because it carries concentrated pathogens and it is the one place in a plant where a Cryptosporidium breakthrough can be recirculated.
A note on sludge quantity, because it governs the site layout: softening produces roughly two kilograms of dry calcium carbonate for every kilogram of hardness precipitated. For a 20 000 m³/d plant removing 215 mg/L of hardness, that is of the order of $20\,000 \times 2 \times 0.215 = 8\,600$ kg/d of dry solids, an order of magnitude more than the coagulation sludge alone would generate. This is the principal reason a utility weighs central softening against point-of-entry alternatives.
| Parameter | Raw water | After treatment | Removal | Governing unit processes | Canadian benchmark |
|---|---|---|---|---|---|
| Turbidity | 150–200 NTU | under 0.1 NTU | 99.9 per cent | Coagulation, flocculation, clarification, dual-media filtration | GCDWQ: 0.3 NTU in 95 per cent of measurements and never above 1.0 NTU for chemically assisted filtration |
| Total hardness | 300 mg/L as CaCO3 | 80–100 mg/L as CaCO3 (design target 85) | about 72 per cent | Lime–soda softening, split treatment, recarbonation | No health-based guideline; 80–100 mg/L is the accepted service target |
| Iron | 1.0 mg/L | under 0.05 mg/L | 95 per cent or better | Pre-oxidation, co-precipitation at high pH, filtration | GCDWQ aesthetic objective 0.3 mg/L |
| Taste and odour | Seasonal geosmin and MIB | Below the odour threshold, about 5 ng/L | — | Pre-oxidation, seasonal PAC, GAC adsorbers | GCDWQ: inoffensive to consumers |
| Pathogens | Present (surface source) | 3-log Giardia, 4-log virus, 3-log Cryptosporidium; total coliforms absent per 100 mL | 99.9 to 99.99 per cent | 2.5-log filtration credit plus chlorine $CT$ credit | GCDWQ minimum treatment goals: 3-log protozoa, 4-log virus; free residual of at least 0.2 mg/L maintained in distribution |
Two design points deserve emphasis. Hardness is deliberately not driven to the practical chemical limit of about 50 mg/L as CaCO3: a fraction of the raw water — about 14 per cent to land on 85 mg/L — is bypassed around the softener and blended back downstream. This split-treatment arrangement saves lime, cuts the sludge volume, and leaves the finished water with enough calcium carbonate saturation to form a protective film rather than attacking the mains. Second, the softening step is a substantial pathogen barrier in its own right: the excess-lime pH of 11 is lethal to bacteria and viruses within minutes, and the calcium carbonate floc enmeshes protozoan cysts, so a lime-softening plant typically earns log credits that a purely coagulation-based plant of the same size would not.