Core principle: apply an external electric field so particles pick up a charge and migrate toward oppositely charged collector plates.
Negatively charged discharge wires (corona wires) ionise the passing gas stream → particles attain a negative charge.
Charged particles drift to the grounded, positively charged plates and accumulate as a dust layer.
Periodic “rapping” dislodges the layer; dust falls into a hopper for removal.
Types:
• Dry ESP (most common)
• Wet ESP (collector surfaces continually or intermittently washed).
Performance: removal efficiency for fine particles typically ≈ 99\%; actual results vary with particle resistivity, gas flow, moisture, power input, and plate spacing.
Operating envelope: flue-gas temperatures up to \approx 700\,^{\circ}!\text{C} (coal plants) with specialised alloys; best with moderate humidity to reduce electrical resistivity.
Typical industrial uses:
• Utility boilers (fly-ash)
• Cement kilns (raw-meal dust)
• Pulp & paper recovery furnaces (salt-cake and lime dust)
• Petrochemical plants (\ce{H2SO4} mist)
• Steel & foundry shops (metal fumes).
Advantages: very low pressure drop, heat recovery possible, capable of continuous operation.
Limitations: high capital cost, performance sensitive to dust resistivity, ozone generation in high-voltage zone, bulky footprint.
Mechanism: dirty gas passes through porous fabric → dust accumulates on the filter cake; filtration is dominated by cake resistance rather than fabric pores once a layer forms.
Filtration mechanisms: interception, inertial impaction, diffusion, electrostatic attraction, and sieving.
Removal efficiency: generally >99\% even for sub-micron particles.
Key design variables: cloth area/air-flow ratio (air-to-cloth ratio), fabric type (cotton, polyester, aramid, PTFE, glass, etc.), cleaning method (pulse-jet, reverse-air, shaker), maximum service temperature, chemical compatibility.
Temperature constraint: gases often cooled to <260\,^{\circ}!\text{C} to protect fabrics → may require dilution air or heat exchangers.
Pros: high efficiency, modular, collects dry dust (easy reuse/disposal).
Cons: sensitive to moisture (clogging), flammable dust hazards, higher pressure drop than ESPs.
Geometry: converging-throat-diverging nozzle accelerates gas to high velocity (typically 60{-}120\,\text{m s}^{-1}) while liquid is injected axially or tangentially.
At throat, atomisation produces fine droplets; collisions/coalescence capture particles.
Exit diffuser slows gas, allowing droplet–particle agglomerates to disengage and fall into separator.
Typical particulate removal: \le 1\,\mu\text{m} particles captured with efficiencies up to 99\% when pressure drop >25\,\text{cm H}_2\text{O}.
Trade-offs: very effective for PM and simultaneous gas absorption, but generates wastewater, imposes high pressure drop (⇒ high fan energy), and requires corrosion-resistant materials.
Utilise centrifugal force: swirling gas creates radial acceleration ar=\tfrac{v{\theta}^2}{r} → particles migrate to wall, lose momentum, and fall to hopper.
Gas path: descending outer vortex + ascending inner vortex; cleaned gas exits through central outlet tube.
Typical efficiency curve:
• >90\% for particles >10\,\mu\text{m}
• Drops sharply below 5\,\mu\text{m}.
Often deployed as a pre-cleaner upstream of ESP or baghouse to reduce dust loading.
Advantages: simple, no moving parts, operates at high temperatures/pressures, low capital cost.
Disadvantages: poor fine-particle capture, erosion at high inlet velocities.
Large, low-velocity boxes allowing residence time so particles settle by gravity: terminal settling velocity vt = \tfrac{(\rhop-\rhog) g dp^2}{18\mu} (Stokes’ law for small Re).
Effective only for coarse particles (>75\,\mu\text{m}); removal efficiencies modest (10–50 %).
Widely used as the first stage to protect downstream equipment.
Objective: convert combustible pollutants (\ce{CO}, \ce{VOC}, \ce{HAP}) to \ce{CO2} and \ce{H2O}.
Governed by the “3 T’s”:
• Temperature – typically 760\text{–}1200\,^{\circ}!\text{C}
• Time (residence) – 0.5\text{–}2\,\text{s}
• Turbulence – ensures thorough mixing.
Sub-categories:
• Recuperative (heat exchanger recovers outlet heat)
• Regenerative (RTO – ceramic beds store/release heat; >95\% heat recovery)
• Direct-flame (enclosed flare).
Regulatory aspects: continuous emission monitors (CEMs) for \ce{CO}, \ce{O2}, hydrocarbons; safety interlocks; auxiliary fuel consumption tracked.
Pros: very high destruction efficiency (>99\% for VOCs).
Cons: high fuel cost, NOx formation, possible dioxin/furan generation if chlorine present.
Purpose: reduce \text{NO}_x (\ce{NO} + \ce{NO2}) to \ce{N2} and \ce{H2O} using a reducing agent (commonly ammonia or urea-derived \ce{NH3}).
Global application: power plants, gas turbines, refinery heaters.
Stoichiometric reactions:
4\,\ce{NO} + 4\,\ce{NH3} + \ce{O2} \;\to\; 4\,\ce{N2} + 6\,\ce{H2O}
6\,\ce{NO2} + 8\,\ce{NH3} \;\to\; 7\,\ce{N2} + 12\,\ce{H2O}
Catalyst: vanadia–titania, zeolite, or precious-metal formulations; optimal 275\text{–}425\,^{\circ}!\text{C}.
Typical overall \text{NO}_x reduction: 70\text{–}90\%; higher possible with fresh catalyst and optimised ammonia mixing.
Side reactions/concerns:
• \ce{SO2 + \tfrac{1}{2} O2 \to SO3} (acid mist formation).
• Ammonia slip leading to \ce{NH4HSO4} deposition (sticky fouling).
• Catalyst deactivation by arsenic, alkalis, dust.
Fundamental distinction:
• Adsorption – molecules adhere to solid surface.
• Absorption – molecules dissolve into bulk liquid.
Commercial adsorbents: activated carbon (surface area 800\text{–}1200\,\text{m}^2\,\text{g}^{-1}), silica gel, activated alumina, molecular sieve zeolites.
Configurations:
• Regenerative – twin-or-multiple beds; whilst one adsorbs, another undergoes thermal or steam desorption.
• Non-regenerative (throw-away) – thin beds; saturated media sent for re-activation or disposal.
Use cases: VOC solvent recovery, odour control, mercury capture, solvent loading docks.
Governing isotherms: Freundlich q = K P^{1/n}, Langmuir q = \tfrac{q_\text{max} bP}{1 + bP} (design for breakthrough time).
Gas species are transferred into a liquid phase; overall rate governed by two-film theory: NA = KL a (C{Ai} - C{Al}).
Liquid of choice: water (cheap, non-toxic) or specialised solutions (alkaline, oxidising, chelating).
Equipment families:
• Spray tower (co-current or counter-current)
• Packed column (random or structured packing)
• Plate column
• Venturi scrubber (dual PM & gas removal).
Typical pollutant targets: \ce{SO2}, \ce{HCl}, \ce{NH3}, water-soluble VOCs.
Removal efficiency: >95\% achievable with adequate liquid-to-gas ratio.
Caveat: creates contaminated liquid effluent → must be treated (chemical neutralisation, biological treatment, crystallisation) to avoid cross-media pollution.
Engineered soil-based or synthetic media beds (compost, wood chips, lava rock, plastic saddles) harbouring mixed microbial consortia.
Polluted air (generally warm & humid, low VOC load, odours) flows upward; compounds diffuse into biofilm and are metabolised mainly to \ce{CO2}, \ce{H2O}, biomass.
Operating conditions:
• Temperature 10\text{–}40\,^{\circ}!\text{C}
• Moisture >40\% wet basis
• pH controlled via nutrient irrigation.
Advantages: low energy and O&M cost, minimal secondary waste.
Limitations: large footprint, sensitive to toxic shocks and drying, limited to water-soluble/biodegradable pollutants.
Physics: condense vapour when T < T{\text{dew}} or P > P{\text{dew}} (Clausius–Clapeyron relation \tfrac{dP}{dT}=\tfrac{L}{T \Delta v}).
Devices:
• Contact condensers – intimate gas/liquid contact (spray, quench).
• Surface condensers – shell-and-tube or plate heat exchangers (no mixing).
Typical removal: 50\% to >95\% depending on coolant temperature and vapour partial pressure.
Often installed as front-end pre-treatment to lower VOC load or recover valuable solvents (e.g.
cryogenic condensation for \ce{CFC} recovery).
Complete oxidation: fuel/air ratio at or above stoichiometric; products ideally \ce{CO2} + \ce{H2O} (plus \ce{N2}).
Classifications:
Direct combustion / Flaring
• No residence chamber; flame open to atmosphere (elevated or ground flare).
• EPA studies → destruction removal efficiency (DRE) \approx 98\% for hydrocarbons if flame stability and mixing maintained.
Thermal incinerator
• Burner + insulated residence chamber (0.5–1.5 s).
• DRE >99\%; supplementary fuel needed if waste gas heating value <930\,\text{kJ m}^{-3}.
Catalytic incinerator
• Downstream catalyst bed (Pt–Pd, Mn–Cu oxides).
• Allows 150\text{–}300\,^{\circ}!\text{C} lower temperature than thermal firing for same DRE (>95\%).
• Susceptible to catalyst poisoning (\ce{Si}, \ce{P}, heavy metals).
Important design metrics:
• Lower heating value (LHV) of waste gas
• Minimum ignition temperature
• Oxygen availability
• Exit \ce{CO} / unburned hydrocarbon levels to satisfy 40 CFR 60.
Pre-cleaners (settling chamber, cyclone) often precede high-efficiency collectors (baghouse, ESP) to minimise wear/fouling and lower pressure drop.
Wet scrubbers simultaneously address PM and soluble gas pollutants (e.g.
\ce{SO2}) but create liquid effluent → remember the “pollution shifting” concept.
The 3 T’s (Temperature, Time, Turbulence) principle re-appears in incineration design – link related calculation problems.
SCR relies on stoichiometric excess ammonia (NH₃/NOₓ ratio 0.9–1.1); know how to compute urea consumption: \ce{(NH2)2CO} + \tfrac{3}{2}\ce{O2} \to 2\ce{CO2} + 2\ce{NH3}.
Condensation vs. Adsorption – both recover solvents; for high concentrations (> several g m⁻³) condensation first, adsorption polishes residual VOC (<100 mg m⁻³).
Efficiency hierarchy for PM (coarse→fine): Settling < Cyclone < Venturi Scrubber ≈ Fabric Filter ≈ ESP.
Always quote efficiency values and governing limitations in design/essay questions.