Water Treatment — Making Drinking Water Safe
Singapore's water treatment plants use a multi-stage process to produce safe drinking water. Chemicals are added at various stages to remove impurities, kill bacteria, and adjust pH. The table below shows data from one treatment plant.
| Stage | Process | Chemical added | Purpose | pH before | pH after |
|---|---|---|---|---|---|
| 1 | Coagulation | Aluminium sulfate Al₂(SO₄)₃ | Clump fine particles together | 7.2 | 6.8 |
| 2 | pH adjustment | Calcium hydroxide Ca(OH)₂ (slaked lime) | Raise pH for optimal coagulation | 6.8 | 7.5 |
| 3 | Chlorination | Chlorine gas Cl₂ | Kill bacteria and pathogens | 7.5 | 7.2 |
| 4 | Fluoridation | Sodium fluoride NaF | Prevent tooth decay (0.5 mg/L) | 7.2 | 7.2 |
- Al³⁺ ions react with water to produce H⁺ ions (hydrolysis), making the solution acidic — pH falls below 7. [1]
- Ion responsible: H⁺ (hydrogen ion / hydronium ion H₃O⁺). [1]
- Ca(OH)₂(s) → Ca²⁺(aq) + 2OH⁻(aq) [1 for correct dissociation equation]
- Ca(OH)₂ is a base — it releases OH⁻ ions in solution [1]
- OH⁻ ions neutralise H⁺ ions (H⁺ + OH⁻ → H₂O), reducing [H⁺] and raising pH above 7 [1]
- Cl₂ + H₂O ⇌ HCl + HClO (hydrochloric acid and hypochlorous acid) [1]
- Both HCl and HClO are acids — they donate H⁺ ions, lowering pH. HClO (hypochlorous acid) is the main disinfecting agent. [1]
- (i) Chloride ion Cl⁻ is present [1]
- (ii) Ag⁺(aq) + Cl⁻(aq) → AgCl(s) [1]
- (iii) Confirms that chlorine (Cl₂) has been added and reacted with water to produce Cl⁻ ions — chlorination has occurred [1]
- Mass of F⁻ required = 0.5 mg/L × 2 000 000 L = 1 000 000 mg = 1000 g [1]
- NaF contains F (19/42 of its mass is F). Mass NaF = 1000 × (42/19) = 2210 g ≈ 2.21 kg [1]
- Moles NaF = mass/Mr = 2210/42 = 52.6 mol [1]
- Benefit: fluoride at 0.5 mg/L strengthens tooth enamel (fluorapatite formation), reducing dental decay (cavities), especially beneficial for children and populations with poor dental care access. [1]
- Risk: at higher concentrations (>1.5 mg/L), fluoride causes dental fluorosis (mottling/discolouration of teeth) and at very high levels can affect bone density (skeletal fluorosis). Requires precise dosing control. [1]
- Evaluation: at the approved level of 0.5 mg/L, the public health benefit (reduced tooth decay) outweighs the risk, provided concentration is accurately monitored. The level is well below the harmful threshold. [1]
Fertiliser Chemistry — Producing Ammonium Nitrate
Ammonium nitrate (NH₄NO₃) is one of the world's most widely used nitrogen fertilisers. It is produced industrially by reacting ammonia (NH₃) with nitric acid (HNO₃). The percentage of nitrogen by mass is a key measure of fertiliser quality. The data below compares common nitrogen fertilisers.
| Fertiliser | Formula | Mr | % N by mass | State at room temp | Solubility in water |
|---|---|---|---|---|---|
| Ammonium nitrate | NH₄NO₃ | 80 | 35.0 | Solid | High |
| Ammonium sulfate | (NH₄)₂SO₄ | 132 | 21.2 | Solid | High |
| Urea | CO(NH₂)₂ | 60 | 46.7 | Solid | High |
| Ammonia solution | NH₃(aq) | 17 | 82.4 | Liquid | Fully miscible |
- NH₄NO₃ contains 2 N atoms: mass of N = 2 × 14 = 28 g per mole [1]
- % N = (28/80) × 100 = 35.0% ✓ [1]
- Mass NH₄NO₃ = required N / (% N / 100) = 60 / 0.350 [1]
- = 171 kg [1]
- Moles NH₃ = 34/17 = 2.0 mol. Mole ratio 1:1 → moles NH₄NO₃ = 2.0 mol [1]
- Mass NH₄NO₃ = 2.0 × 80 = 160 g [1]
- Moles HNO₃ needed = 2.0 mol. Volume = moles/c = 2.0/2.0 = 1.0 dm³ = 1000 cm³ [1]
- Ammonium nitrate releases nitrogen in two forms: NH₄⁺ (ammonium, slow release, held in soil) and NO₃⁻ (nitrate, immediately available to plants) — providing both immediate and sustained nutrition. Urea must first be hydrolysed to ammonium by soil bacteria, which takes time. [1]
- Ammonium nitrate is more acidic and can be used to adjust soil pH for acid-loving crops. Urea is neutral/slightly alkaline after hydrolysis. [1]
- Urea releases ammonia gas on warm, moist soils (volatilisation loss) — nitrogen is lost to the atmosphere. Ammonium nitrate has lower volatilisation losses. [1]
- Excess nitrates and phosphates in the river act as nutrients, causing rapid growth of algae on the water surface (algal bloom). [1]
- The algae block sunlight, killing aquatic plants below. When the algae die, aerobic decomposing bacteria multiply and consume large amounts of dissolved oxygen (BOD increases). [1]
- The dissolved oxygen level in the water falls severely. Fish and other aquatic organisms cannot get enough oxygen and suffocate/die. [1]
- Ionic equation: H⁺(aq) + OH⁻(aq) → H₂O(l) [1] (Ca²⁺ is spectator ion)
- At pH 5.2, many essential minerals (such as phosphate and molybdenum) are insoluble or unavailable to plant roots. Raising pH increases availability of nutrients [1]
- Very acidic soils also allow toxic ions (e.g. Al³⁺, Mn²⁺) to dissolve, which damage plant root cells. Neutralisation removes these toxic ions by precipitating them as hydroxides. [1]
Food Chemistry — Fats, Oils and Energy
Fats and oils are esters formed from glycerol and three fatty acid chains. They are an important energy source. The table compares three common fatty acids found in food.
| Fatty acid | Formula | Number of C=C double bonds | Melting point (°C) | Source |
|---|---|---|---|---|
| Stearic acid (saturated) | C₁₇H₃₅COOH | 0 | 69 | Animal fat (beef, lamb) |
| Oleic acid (monounsaturated) | C₁₇H₃₃COOH | 1 | 13 | Olive oil, avocado |
| Linolenic acid (polyunsaturated) | C₁₇H₂₉COOH | 3 | -11 | Flaxseed, walnuts |
- As the number of C=C double bonds increases, the melting point decreases: 0 bonds → 69°C; 1 bond → 13°C; 3 bonds → −11°C. [1]
- C=C double bonds cause kinks (bends) in the carbon chain. More double bonds = more bends, preventing molecules from packing closely together. [1]
- Molecules that are further apart have weaker intermolecular (van der Waals) forces between them → less energy needed to overcome these forces → lower melting point. [1]
- Oleic acid: bromine water is decolourised (orange to colourless) — Br₂ adds across the C=C double bond by addition reaction. [1]
- Stearic acid: bromine water remains orange/brown — no C=C double bonds present, so no addition reaction occurs. [1]
- C₁₇H₂₉COOH + 2H₂ → C₁₇H₃₃COOH [1] (2 moles H₂ added to convert 2 of the 3 double bonds)
- Conditions: hydrogen gas (H₂), nickel catalyst, temperature ~180°C [1]
- (i) Q = mcΔT = 500 × 4.2 × (37.4 − 20.0) = 500 × 4.2 × 17.4 = 36 540 J = 36.5 kJ per gram [1]
- (ii) Energy per mole = 36.5 kJ/g × 284 g/mol = 10 366 kJ/mol ≈ 10 400 kJ/mol [1 calculation, 1 answer with unit]
- Saturated fats have no C=C double bonds — straight chain molecules pack closely together and are solid at room temperature. In blood vessels, they can contribute to solid deposits (atherosclerotic plaques) that narrow arteries. [1]
- Unsaturated fats have C=C double bonds causing kinks — molecules cannot pack as closely, remain liquid at body temperature and are more easily metabolised. They do not form solid deposits as readily. [1]
- The chemistry supports the health claim — structure difference (saturated vs unsaturated) leads to different physical behaviour (solid vs liquid at body temperature) which correlates with different metabolic effects. [1]
- Limitation: chemistry alone does not prove causation for heart disease — other factors (genetics, total calorie intake, exercise, trans fats) also contribute. The claim is supported by chemistry but not conclusively proven by chemistry data alone. [1]
The Chlor-Alkali Industry — Electrolysis of Brine
The electrolysis of concentrated sodium chloride solution (brine) is one of the most important industrial chemical processes. It produces three useful products: chlorine gas (Cl₂), hydrogen gas (H₂), and sodium hydroxide solution (NaOH). A plant electrolyses brine using a current of 50 000 A continuously.
| Product | Electrode | Electrode equation | Annual production (tonnes) | Main uses |
|---|---|---|---|---|
| Chlorine (Cl₂) | Anode (+) | 2Cl⁻ → Cl₂ + 2e⁻ | 45 000 | PVC plastic, disinfectants, bleach |
| Hydrogen (H₂) | Cathode (−) | 2H₂O + 2e⁻ → H₂ + 2OH⁻ | 1 300 | Fuel cells, margarine production, ammonia synthesis |
| Sodium hydroxide (NaOH) | Cathode region | Na⁺ + OH⁻ (from cathode reaction) | 50 000 | Soap making, paper, cleaning products |
- Anode: Cl⁻ is oxidised (loses electrons) → Cl₂. Cathode: H₂O is reduced (gains electrons) → H₂ + OH⁻. [1]
- In concentrated brine, Cl⁻ ions greatly outnumber OH⁻ ions near the anode → Cl⁻ ions are more likely to be discharged. In dilute solution, OH⁻ would be preferentially discharged (O₂ produced). The high concentration of Cl⁻ is essential — this is why concentrated brine is used. [1]
- (i) Q = It = 50 000 × 3600 = 1.8 × 10⁸ C [1]
- (ii) Moles e⁻ = Q/F = 1.8×10⁸ / 96 500 = 1865 mol [1]
- (iii) From equation: 2e⁻ → 1 Cl₂. Moles Cl₂ = 1865/2 = 932.5 mol [1]
- (iv) Mass Cl₂ = 932.5 × (2×35.5) = 932.5 × 71 = 66 208 g ≈ 66.2 kg per hour [1]
- Moles Cl₂ = 71/71 = 1 mol [1]
- Mole ratio Cl₂ : NaOH = 1 : 2. Moles NaOH needed = 2 mol [1]
- Volume = moles/c = 2/2.0 = 1.0 dm³ = 1000 cm³ [1]
- (i) Environmental benefit: chlorine is used to disinfect drinking water and swimming pools — prevents waterborne diseases, saving millions of lives. NaOH is used in paper recycling. [1]
- (ii) Environmental concern: large electricity consumption → if powered by fossil fuels, significant CO₂ emissions. Chlorine gas is extremely toxic — leaks pose serious environmental and health hazards. Disposal of brine and mercury (from older mercury cell processes) can contaminate water. [1]
- (iii) Economic importance: all three products are high-volume industrial chemicals. Cl₂ → PVC, pharmaceuticals, solvents (global market >$50 bn). NaOH → soap, paper, aluminium processing. H₂ → emerging hydrogen economy, fuel cells. The process is economically vital to the chemical industry. [1]
- (iv) Sustainability improvement: power the electrolysis with renewable energy (solar/wind) to eliminate CO₂ emissions from electricity generation. Or: use membrane cell technology (instead of older mercury or diaphragm cells) which produces purer NaOH with no mercury pollution. [1]
- [1 for coherent overall evaluation connecting all four points]
The Haber Process — Industrial Ammonia Synthesis
Ammonia (NH₃) is produced industrially by the Haber process: N₂(g) + 3H₂(g) ⇌ 2NH₃(g). The reaction is reversible and exothermic (ΔH = −92 kJ/mol). Industrial conditions are chosen to balance rate and yield. The table below shows how yield and rate vary with temperature and pressure.
| Temperature (°C) | Equilibrium yield of NH₃ (%) | Rate of reaction |
|---|---|---|
| 200 | 60 | Very slow |
| 350 | 40 | Slow |
| 450 | 17 | Moderate (industrial choice) |
| 550 | 8 | Fast |
- 200°C gives a high yield (60%) but the rate is very slow — ammonia would be produced too slowly to be economically viable, and the energy cost of maintaining the reactor would be disproportionate to the output. [1]
- 550°C gives a fast rate but only 8% yield — most of the N₂ and H₂ would be wasted. 450°C is a compromise: a moderate rate (economically practical) with a reasonable yield (17%) — unreacted gases are recycled to improve overall efficiency. [1]
- (i) Temperature — The forward reaction is exothermic. Increasing temperature favours the ENDOTHERMIC (reverse) reaction by Le Chatelier's principle → equilibrium shifts left → less NH₃ (lower yield). However, higher temperature gives particles more kinetic energy → more frequent collisions AND more particles exceed activation energy → faster rate. Rate and yield act in opposite directions with temperature. [1]
- (ii) Pressure — Left side has 4 mol gas (1 N₂ + 3 H₂); right side has 2 mol gas (2 NH₃). Increasing pressure favours the side with fewer gas molecules (right) → equilibrium shifts right → more NH₃ (higher yield). Higher pressure also increases particle concentration → more frequent collisions → faster rate. Both rate and yield improve with pressure. [2]
- Heterogeneous: the catalyst (solid iron) is in a different physical state from the reactants (gases). The reaction occurs on the surface of the solid catalyst. [1]
- The catalyst provides an alternative reaction pathway with lower activation energy — more molecules have sufficient energy to react → faster rate. Since the catalyst lowers Ea equally for both forward and reverse reactions, the equilibrium position (and therefore yield) is unchanged — equilibrium is reached faster but the same yield results. [1]
- (i) Volume NH₃ = 17% × 1200 = 204 dm³ [1]
- (ii) Moles NH₃ = 204/24 = 8.5 mol [1]
- (iii) Mass NH₃ = 8.5 × 17 = 144.5 g [1] (Mr of NH₃ = 14+3 = 17)
- (i) Oxidation — NH₃ is oxidised (gains oxygen / loses hydrogen). The oxidation state of N increases from −3 in NH₃ to +2 in NO. Catalytic oxidation using platinum/rhodium catalyst at 900°C. [1]
- (ii) The Haber process fixes atmospheric nitrogen into ammonia, which can be converted to fertilisers that dramatically increase crop yields. Without artificial fertilisers, global food production could not sustain the current world population of 8 billion+. The process is essential to modern food security. [1]
- (iii) Any one of: nitrate run-off from fields causes eutrophication of waterways (algal blooms, fish death) / release of N₂O (a potent greenhouse gas) from soil bacteria acting on nitrogen fertilisers / over-application acidifies soil / groundwater contamination with nitrates (linked to health risks at high concentrations). [1]
- [1 for coherent and well-developed answer connecting all three parts]