UNIT 3: WASTEWATER TREATMENT & AIR POLLUTION CONTROL
1.0 Fundamentals of Wastewater Treatment
Unit Operations and Processes
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Unit Operations: Physical processes where only physical forces are involved. No chemical or biological change occurs.
- Examples: Screening, Grit removal, Sedimentation, Flotation, Filtration, Adsorption.
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Unit Processes: Chemical or biological processes that bring about a change in the wastewater quality.
- Examples: Chemical coagulation, Disinfection, Biological oxidation (Activated sludge, Trickling filters).
Role of Micro-organisms in Biological Treatment
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Heterotrophic Bacteria: Decompose organic matter (BOD/COD) using organic carbon as energy source. Primary agents in carbonaceous BOD removal.
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Autotrophic Bacteria: Obtain energy from inorganic compounds (e.g., ammonia, nitrite). Crucial for nitrification (ammonia → nitrite → nitrate).
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Protozoa & Metazoa: Consume bacteria and suspended solids, improving effluent clarity and acting as indicators of sludge health.
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Process: Microorganisms form flocs (activated sludge) or biofilms (trickling filters) that can be separated from treated water.
2.0 Preliminary Treatment
Racks and Screens
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Purpose: Remove large floating solids (rags, sticks, plastics) to protect pumps and downstream equipment.
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Types:
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Coarse Screens: Bar spacing 50-150 mm.
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Fine Screens: Bar spacing 6-25 mm.
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Microscreens: Bar spacing < 6 mm.
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Head Loss through Bar Screens: Estimated by Kern's formula:
$$h_f = \frac{1}{2} \frac{b}{a} \frac{v^2}{2g} \left( \frac{\sin \theta}{\cos^2 \theta} \right) \left( \frac{n}{n - \frac{b}{a}} \right)^{4/3}$$
Where:
* `a` = clear spacing between bars (m)
* `b` = bar thickness (m)
* `v` = approach velocity (m/s)
* `θ` = angle of screen with horizontal
* `n` = number of bars
> [!TIP] For exams, remember the simplified form: $$\displaystyle h_f = \beta \frac{v^2}{2g} $$, where $\beta$ is a loss coefficient depending on screen geometry.
Grit Chamber
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Purpose: Remove sand, gravel, cinders, and other inorganic solids (grit) to prevent abrasion and deposition in pipes and tanks.
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Design Principle: Based on horizontal flow velocity ($$\displaystyle V_h $$) and settling velocity ($$\displaystyle v_s $$) of target grit particles.
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$$\displaystyle V_h $$ is kept low enough to allow grit to settle but high enough to prevent organic matter from settling.
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Standard $$\displaystyle V_h $$: 0.15 - 0.3 m/s.
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Settling Velocity ($$\displaystyle v_s $$): For discrete particles, calculated by Stokes' Law (for laminar flow, Re < 1):
$$v_s = \frac{g (s-1) d^2}{18 \nu}$$
Where `s` = specific gravity, `d` = diameter (m), `ν` = kinematic viscosity (m²/s).
For turbulent flow, use Newton's or intermediate regime formulas.
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Rectangular Grit Chamber Design: Key parameters are length (L), width (W), and depth (D).
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Detention time: 60-90 seconds.
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$$\displaystyle L = V_h \times t $$ (where
tis detention time). -
$$\displaystyle W = Q / (D \times V_h) $$.
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$D$ is chosen to keep $$\displaystyle V_h $$ within limits.
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3.0 Primary Treatment
Sedimentation
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Purpose: Remove settleable organic and inorganic solids (primary sludge) and floating matter (scum) by gravity.
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Types of Settling:
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Discrete Settling: Particles settle as isolated entities (e.g., sand in grit chamber). Settling velocity constant.
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Flocculent Settling: Particles flocculate during settling, increasing mass and settling velocity (most common in primary tanks).
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Hindered Settling: High particle concentration creates a "blanket" where settling is hindered by upward flow of displaced water.
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Compression Settling: Under high load, sludge at the bottom is compressed by weight of overlying sludge.
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Design of Rectangular Sedimentation Tank
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Key Parameters:
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Surface Loading Rate (SLR): $$\displaystyle q_o = Q / A $$ (m³/m².day). Typical: 100-200 m³/m².day for plain sedimentation.
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Detention Time (t): $$\displaystyle t = V / Q $$. Typical: 1.5-2.5 hours.
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Length:Width Ratio: 3:1 to 5:1.
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Depth: 2-4.5 m.
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Design Steps:
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Determine
Q(peak flow). -
Select
q_oandt. -
Calculate Area $$\displaystyle A = Q / q_o $$.
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Choose
L:Wratio → findLandW. -
Calculate Volume $$\displaystyle V = A \times D $$ and check $$\displaystyle t = V/Q $$.
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Provide inlet/outlet devices to distribute flow and prevent short-circuiting.
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Septic Tank vs Imhoff Tank
| Feature | Septic Tank | Imhoff Tank |
|---|---|---|
| Scope | Single unit for primary treatment & digestion. | Two-story unit: upper sedimentation, lower sludge digestion. |
| Function | Raw sewage enters, solids settle & undergo anaerobic digestion in same compartment. Effluent is septic. | Settling occurs in upper chamber; sludge slides to lower chamber for separate anaerobic digestion. |
| Performance | Effluent has high BOD, solids, and pathogens. Requires further treatment. Poor sludge digestion due to mixing. | Better effluent quality than septic tank. More efficient sludge digestion due to separate, quiescent zone. |
| Sludge Handling | Sludge accumulates and must be removed periodically (every 2-5 years). Digestion is incomplete. | Sludge digestion is more complete; supernatant liquor returns to upper tank; sludge removal less frequent. |
| Application | Small communities, isolated buildings. | Larger communities where some treatment is needed but conventional plants are not feasible. |
Chemical Coagulation (Alum Dosing)
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Purpose: Add coagulants (e.g., alum - $$\displaystyle Al_2(SO_4)_3.14H_2O $$) to destabilize colloidal particles and form larger flocs for removal in sedimentation/filtration.
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Alum Dose Calculation:
$$\text{Alum required (kg/day)} = \frac{\text{Dose (mg/L)} \times \text{Flow (ML/day)}}{1000}$$
> [!TIP] Example: Dose = 28.6 mg/L, Flow = 18 ML/day → Alum = $$\displaystyle (28.6 \times 18) / 1000 = 0.5148 $$ tonnes/day.
4.0 Secondary Treatment Processes
Trickling Filters
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Working Principle: Wastewater is sprayed over a packed bed of rocks/plastic media. A biological film (slime) grows on media. As wastewater trickles down, organic matter is oxidized by aerobic microorganisms in the film. Excess film sloughs off and is removed in a settling tank.
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Types:
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Standard Rate: Low organic loading (40-100 g BOD/m².day), deeper (2-3 m), lower efficiency (80-85% BOD removal).
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High Rate: High organic loading (100-400 g BOD/m².day), shallower (1-2 m), requires recirculation, higher efficiency.
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Design Parameters:
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Surface Loading Rate (Organic Loading): $$\displaystyle L_s = \frac{Q \times L_0}{A} $$ (g BOD/m².day), where $$\displaystyle L_0 $$ = influent BOD (mg/L).
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Depth: 0.6-2.4 m (high rate to standard).
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Efficiency Determination (NRC Formula):
$$E = 100 \left[ 1 - \frac{1}{1 + k_d \left( \frac{V}{Q} \right)} \right]$$
Where:
* `E` = % BOD removal
* `k_d` = filter rate constant (day⁻¹), depends on temperature and filter type.
* `V/Q` = hydraulic detention time in filter (days).
Activated Sludge Process
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Description: Wastewater is aerated in an aeration tank with a dense suspension of microorganisms (activated sludge). The mixture flows to a secondary clarifier where sludge is settled. Part of the sludge is recycled (Return Activated Sludge - RAS) to maintain biomass; excess is wasted (Waste Activated Sludge - WAS).
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Flow Diagram Sketch:
[Influent] → [Aeration Tank (Air diffusers)] → [Secondary Clarifier] → [Effluent]&[RAS] → Aeration Tank,[WAS] → Sludge Handling. -
Oxygen Requirements Calculation:
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Theoretical Oxygen Demand: For BOD oxidation: $$\displaystyle CH_2O + O_2 \rightarrow CO_2 + H_2O $$. 1 mg BOD ≈ 1 mg O₂.
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Practical Requirement: $$\displaystyle O_2 $$ required (kg/day) = $$\displaystyle Q \times (L_0 - L_e) \times \text{Factor} $$.
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Factor accounts for endogenous respiration, nitrification (if occurring), and inefficiencies. Typical: 1.3 - 1.5 for carbonaceous BOD removal.
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Air Supply: $$\displaystyle Air (m³/min) = \frac{O_2 \text{ required (kg/day)} \times 1000}{0.21 \times 60 \times 24 \times \rho_{air}} $$, where $$\displaystyle \rho_{air} \approx 1.2 $$ kg/m³.
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Oxidation Ditch
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Working: A modified extended aeration activated sludge system. It's an oval-shaped, continuous-flow channel (ditch) equipped with surface aerators (rotors or brushes) that provide both aeration and circulation. It operates at very long SRT (> 20 days), promoting complete oxidation and nitrification.
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Sketch:
DiagramSEARCH: oxidation ditch configuration with rotor and clarifier -
Configurations:
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Single Ditch: One oval channel with one or more aerators.
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Tandem Ditch: Two or more ditches in series.
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Parallel Ditch: Multiple ditches operating in parallel for redundancy.
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Carrousel System: A branded type with multiple rotor positions.
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5.0 Advanced/Tertiary Treatment
Nitrogen Removal
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Biological Nitrification-Denitrification:
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Nitrification (Aerobic): $$\displaystyle NH_4^+ + 1.5O_2 \rightarrow NO_2^- + 2H^+ + H_2O $$ (by Nitrosomonas); $$\displaystyle NO_2^- + 0.5O_2 \rightarrow NO_3^- $$ (by Nitrobacter).
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Denitrification (Anoxic): $$\displaystyle NO_3^- \rightarrow N_2 $$ (gas) by heterotrophic bacteria using organic carbon as electron donor. Requires anoxic zone (DO ≈ 0 mg/L).
- Process Configurations: Bardenpho, Modified Ludzack-Ettinger (MLE), SBR, Oxidation Ditch with anoxic zones.
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Ammonia Stripping:
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Principle: Raise pH (> 10.5) using lime to convert ammonium ($$\displaystyle NH_4^+ $$) to free ammonia ($$\displaystyle NH_3 $$). Air is blown counter-current through the wastewater in a stripping tower, volatilizing $$\displaystyle NH_3 $$. The air is then absorbed in an acid (e.g., $$\displaystyle H_2SO_4 $$) to recover ammonia as ammonium sulfate.
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Limitation: Scaling/fouling, high chemical cost, sensitivity to temperature.
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Advanced Wastewater Treatment (AWT)
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Definition: Treatment beyond secondary (biological) level to remove nutrients (N, P), non-biodegradable organics, pathogens, and total dissolved solids (TDS) to very high standards for reuse or sensitive discharge.
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Comparison with Conventional Treatment:
| Feature | Conventional (Primary + Secondary) | Advanced (Tertiary) | | :--- | :--- | :--- | | Goal | BOD, SS removal to ~30 mg/L. | N, P, TDS, pathogens to < 5-10 mg/L. | | Processes | Screening, Sedimentation, Biological (AS/TF). | Chemical precipitation, Filtration, Membrane, Disinfection, Adsorption. | | Cost | Moderate. | High (capital & O&M). | | Reuse | Limited (irrigation). | High (industrial, potable, groundwater recharge). |
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Important AWT Processes (Tabulation):
| Process | Purpose | Key Mechanism | | :--- | :--- | :--- | | Chemical Precipitation | Phosphorus removal | Addition of alum/ferric chloride/lime to form insoluble phosphates. | | Sand/Multimedia Filtration | Remove residual SS | Physical straining. | | Activated Carbon Adsorption | Remove organics, taste/odor | Adsorption onto porous carbon. | | Membrane Filtration | Remove TDS, colloids, pathogens | Ultrafiltration (UF), Reverse Osmosis (RO). | | Disinfection | Pathogen kill | Chlorination, Ozonation, UV. | | Ion Exchange | Remove specific ions (e.g., $$\displaystyle Na^+ $$, $$\displaystyle Cl^- $$) | Exchange with resin ions. |
Filtration Methods
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Diatomaceous Earth Filter:
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Medium: Filter aid made from fossilized diatoms (siliceous). Forms a thin precoat on a septum.
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Operation: Body feed of DE slurry added during filtration to maintain precoat thickness. Removes very fine particles (1-3 µm).
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Application: Polishing filter after coagulation/filtration for high-quality effluent.
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Ultrafiltration (UF):
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Mechanism: Membrane filtration with pore size 0.01-0.1 µm. Removes colloids, macromolecules, bacteria, and viruses. Operates on size exclusion.
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Driving Force: Pressure (1-10 bar).
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Advantages: No chemical addition, compact, high removal efficiency.
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Limitations: Membrane fouling, high capital cost, concentrates (retentate) require disposal.
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6.0 Air Pollution Fundamentals
Air Pollutants
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Classification & Characteristics:
| Pollutant | Primary Sources | Key Characteristics & Health Effects | | :--- | :--- | :--- | | Sulphur Dioxide (SO₂) | Fossil fuel combustion (coal/oil), smelting. | Colorless, pungent, soluble in water → acid rain. Irritates respiratory tract, aggravates asthma. | | Hydrogen Sulphide (H₂S) | Anaerobic decomposition (sewage, swamps), petroleum refining. | Colorless, rotten egg smell, toxic (olfactory fatigue). Respiratory paralysis at high conc. | | Particulate Matter (PM) | Combustion, construction, agriculture. RSPM (Respirable, <10µm) vs TSPM (Total Suspended, <100µm). | RSPM penetrates deep lungs (alveoli), causes bronchitis, asthma, lung cancer. TSPM includes larger particles (soot, dust). |
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Primary vs Secondary Pollutants:
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Primary: Emitted directly from source (e.g., $$\displaystyle SO_2 $$, $$\displaystyle NO_x $$, CO, PM).
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Secondary: Formed in atmosphere by chemical reactions of primary pollutants (e.g., $$\displaystyle O_3 $$, $$\displaystyle H_2SO_4 $$, $$\displaystyle HNO_3 $$, $PAN$).
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Aerosols: Solid or liquid particles suspended in gas (air). Types:
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Dust: >1 µm, settles quickly.
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Fume: <1 µm, formed by condensation.
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Fog/Mist: Liquid droplets.
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Smoke: From incomplete combustion.
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Smog: Mixture (e.g., photochemical smog).
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Meteorological Factors
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Temperature Lapse Rate (ELR vs ALR):
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Environmental Lapse Rate (ELR): Actual rate of temperature decrease with height in the atmosphere. Varies with time/place (average ~6.5°C/km).
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Adiabatic Lapse Rate (ALR): Temperature change of a parcel of air rising/falling without heat exchange. Dry ALR = 9.8°C/km. Saturated ALR ≈ 5-6°C/km (due to latent heat release).
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Stability: If ELR < ALR → stable (inversion, poor dispersion). If ELR > ALR → unstable (good dispersion).
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Factors Influencing Dispersion:
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Wind speed & direction.
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Atmospheric stability (lapse rate).
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Mixing height (depth of turbulent layer).
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Topography (valleys trap pollutants).
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Precipitation (scavenges pollutants).
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Air Pollution Dispersion Models
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Gaussian Plume Model:
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Assumptions: Steady-state, constant emissions, flat terrain, no deposition/chemical reaction, wind speed constant with height.
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Equation for Ground-Level Concentration ($C$) at downwind distance
x:
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$$C(x,y,z=0) = \frac{Q}{2\pi \sigma_y \sigma_z U} \exp\left(-\frac{y^2}{2\sigma_y^2}\right) \left[ \exp\left(-\frac{H^2}{2\sigma_z^2}\right) + \exp\left(-\frac{H^2}{2\sigma_z^2}\right) \right]$$
Where:
* `Q` = emission rate (g/s)
* `U` = wind speed (m/s)
* `H` = effective stack height (m)
* `σ_y`, `σ_z` = dispersion parameters (depend on downwind distance `x` and atmospheric stability).
* `y` = lateral distance from plume centerline.
* `z` = vertical height.
* For **ground-level source (H=0)**, equation simplifies.
- Location of Maximum Concentration: For a ground-level source, maximum occurs directly downwind at
xwhere $$\displaystyle \sigma_z $$ is smallest (initially). For an elevated stack, maximum ground-level concentration occurs at a downwind distance $$\displaystyle x_{max} \approx H / \tan \theta $$, where $\theta$ is the vertical spread angle. The maximum concentration itself is:
$$C_{max} \approx \frac{2Q}{\pi H^2 U} \cdot \frac{\sigma_y}{\sigma_z} \text{ (at } y=0\text{)}$$
Specific Air Pollution Phenomena
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Photochemical Smog:
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Formation: In sunny, stagnant conditions, $$\displaystyle NO_x $$ and VOCs (from vehicles/solvents) react in presence of sunlight to form ozone ($$\displaystyle O_3 $$), PANs, aldehydes, etc.
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Characteristics: Brownish haze, eye irritation, plant damage, rubber cracking. Typical in Los Angeles-type basins.
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Industrial Emission Estimation
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Power Plant Calculations (Flyash, Bottom Ash, SO₂):
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Coal Consumption Rate: $$\displaystyle M_c = \frac{\text{Plant Output (MW)} \times 24 \times 3600 \times 10^6}{\eta \times \text{CV (MJ/kg)} \times 10^6} $$ kg/day.
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η= overall efficiency (decimal). -
CV= calorific value (MJ/kg).
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Ash Content: $$\displaystyle M_{ash} = M_c \times \frac{\text{% Ash}}{100} $$ kg/day.
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Flyash & Bottom Ash: Given % flyash in total ash. $$\displaystyle M_{flyash} = M_{ash} \times \frac{\text{% Flyash}}{100} $$. $$\displaystyle M_{bottom} = M_{ash} - M_{flyash} $$.
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Recoverable Ash: Apply recovery % to flyash and bottom ash separately.
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SO₂ Emission: $$\displaystyle M_{SO2} = 2 \times M_c \times \frac{\text{% S}}{100} \times \frac{32}{32} $$ (since S → SO₂, molecular weight ratio ≈ 2).
- More precisely: $$\displaystyle M_{SO2} = 2 \times \frac{32}{32} \times M_c \times (\%S/100) $$.
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Air Pollution Control Methods
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Adsorption by Activated Carbon:
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Mechanism: Organic vapors/gases adhere to porous surface of activated carbon via van der Waals forces.
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Process: Fixed bed adsorber. Carbon can be regenerated by steam/heat.
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Application: Control of VOCs, odours, $$\displaystyle H_2S $$, $$\displaystyle SO_2 $$ (with impregnation).
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Other Methods:
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Stripping: Mass transfer from liquid to gas phase (e.g., ammonia stripping from wastewater).
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Filtration: Particulate control (baghouse, ESP, cyclone).
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7.0 High-Frequency Short Note Topics
Photochemical Smog
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Definition: A type of smog formed by the reaction of sunlight with nitrogen oxides ($$\displaystyle NO_x $$) and volatile organic compounds (VOCs).
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Formation: $$\displaystyle NO_2 \xrightarrow{h\nu} NO + O $$; $$\displaystyle O + O_2 \rightarrow O_3 $$; $$\displaystyle O_3 + VOC \rightarrow PANs $$, aldehydes, etc.
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Characteristics: Brownish haze, high oxidant content ($$\displaystyle O_3 $$, PAN), occurs in sunny, warm afternoons, causes eye/respiratory irritation, plant damage. Typical of Los Angeles.
Temperature Lapse Rate (ELR vs ALR)
| Parameter | Environmental Lapse Rate (ELR) | Adiabatic Lapse Rate (ALR) |
|---|---|---|
| Definition | Actual rate of temperature decrease with altitude in the atmosphere. | Temperature change of a parcel of air rising/falling adiabatically (no heat exchange). |
| Value | Variable (avg ~6.5°C/km). | Dry: 9.8°C/km. Saturated: ~5-6°C/km. |
| Dependence | On time, location, weather. | Constant for dry/saturated air (thermodynamic property). |
| Role in Dispersion | Determines atmospheric stability. If ELR < ALR → stable/ inversion (poor dispersion). If ELR > ALR → unstable (good dispersion). |
Gaussian Plume Model
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Purpose: Predict pollutant concentration downwind of a continuous point source (stack).
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Core Equation (for elevated stack, ground-level receptor):
$$C(x,y,z=0) = \frac{Q}{2\pi \sigma_y \sigma_z U} \exp\left(-\frac{y^2}{2\sigma_y^2}\right) \left[ \exp\left(-\frac{(H)^2}{2\sigma_z^2}\right) + \exp\left(-\frac{(H)^2}{2\sigma_z^2}\right) \right]$$
* `Q`: emission rate (g/s)
* `U`: wind speed (m/s)
* `H`: effective stack height (physical height + plume rise)
* `σ_y`, `σ_z`: lateral & vertical dispersion coefficients (from Pasquill-Gifford curves, depend on `x` and stability class).
- Location of Max Concentration: For a given
x, max occurs aty=0(plume centerline). The downwind distance of peak ground-level concentration for an elevated stack is approximately $$\displaystyle x_{max} \approx H / \tan \theta $$, where $\theta$ relates to $$\displaystyle \sigma_y/\sigma_z $$ ratio.
Diatomaceous Earth Filter
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Medium: Filter aid composed of fossilized diatom skeletons (silica).
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Operation: A precoat is formed on a filter septum (cloth/mesh). During filtration, a slurry of DE (body feed) is added continuously to replenish the precoat and prevent clogging.
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Pore Size: Very fine (1-3 µm). Removes particles much smaller than sand filters.
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Application: Polishing filter for high-purity water/wastewater effluent, often after coagulation/sedimentation. Common in swimming pools and pharmaceutical industries.
Ultrafiltration (UF)
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Mechanism: Pressure-driven membrane separation with pore size 0.01-0.1 µm.
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Removes: Colloids, macromolecules, bacteria, viruses, some endotoxins. Does not remove dissolved ions/salts (unlike RO).
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Driving Force: Hydraulic pressure (1-10 bar).
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Configuration: Spiral wound, hollow fiber, tubular.
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Advantages: No chemical addition, compact, high and consistent quality.
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Limitations: Membrane fouling/scaling, high energy cost, concentrate disposal.
Ammonia Stripping Method
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Principle: Convert soluble ammonium ion ($$\displaystyle NH_4^+ $$) to volatile ammonia gas ($$\displaystyle NH_3 $$) by raising pH > 10.5 (using lime), then strip with air.
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Process: Air is blown counter-current through a packed tower (stripper) containing high-pH wastewater. $$\displaystyle NH_3 $$ is transferred to air stream. The air is then passed through an acid (e.g., $$\displaystyle H_2SO_4 $$) absorber to recover ammonia as ammonium sulfate fertilizer.
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Key Issues: Scaling/fouling from carbonate precipitation, high lime cost, temperature sensitivity (stripping efficiency drops in winter), odour control needed.
RSPM vs TSPM
| Feature | RSPM (PM₁₀) | TSPM |
|---|---|---|
| Definition | Respirable Suspended Particulate Matter. Particles with aerodynamic diameter ≤ 10 µm. | Total Suspended Particulate Matter. All particles with aerodynamic diameter ≤ 100 µm suspended in air. |
| Health Impact | Penetrates deep into alveolar region of lungs. Causes bronchitis, asthma, lung cancer, cardiovascular diseases. | Larger particles trapped in upper respiratory tract (nose, throat). Less severe health impact but causes soiling, nuisance. |
| Sources | Combustion (vehicles, power plants), industrial processes, secondary aerosol formation. | Includes RSPM + larger dust from construction, roads, agriculture, natural sources. |
| Regulatory Focus | Primary air quality standard (e.g., NAAQS in India) due to severe health effects. | Less stringent standards; often monitored for general air quality. |
Factors Affecting Air Pollution Dispersion
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Wind Speed & Direction: Higher speed → faster dilution. Direction determines impact zone.
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Atmospheric Stability: Determined by lapse rate. Stable (inversion) → poor vertical mixing, high concentrations. Unstable → good mixing.
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Mixing Height: Height of the turbulent boundary layer. Low mixing height (night, winter) traps pollutants near ground.
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Topography: Valleys, basins trap pollutants (e.g., Los Angeles, Delhi). Hills cause downwash.
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Precipitation: Rain/snow efficiently scavenges particles and soluble gases ("wet deposition").
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Surface Roughness: Urban areas (buildings) increase turbulence, enhance dispersion but create recirculation zones.
Primary vs Secondary Air Pollutants
| Primary Pollutants | Secondary Pollutants | |
|---|---|---|
| Definition | Emitted directly from identifiable sources. | Formed in the atmosphere by chemical/photochemical reactions of primary pollutants. |
| Examples | $$\displaystyle SO_2 $$, $$\displaystyle NO_x $$, CO, $PM$, $VOCs$, $$\displaystyle H_2S $$. | $$\displaystyle O_3 $$ (ground-level), $$\displaystyle H_2SO_4 $$, $$\displaystyle HNO_3 $$, $PAN$ (Peroxyacetyl nitrate), sulfate/nitrate aerosols. |
| Control Strategy | Control at source (end-of-pipe, fuel switching). | Control precursor emissions (e.g., control $$\displaystyle NO_x $$ & VOCs to reduce $$\displaystyle O_3 $$). |
Effect of Air Pollution on Materials
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Corrosion: $$\displaystyle SO_2 $$, $$\displaystyle NO_x $$, acid rain accelerate corrosion of metals (steel, copper), limestone, marble (e.g., historical monuments).
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Soiling & Discoloration: Deposition of soot, dust, and aerosols on buildings, fabrics, paintings.
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Degradation: Ozone and other oxidants cause cracking of rubber, fading of dyes, deterioration of paints and plastics.
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Erosion: Acidic deposition leaches protective layers from stone and concrete.
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Economic Impact: Increased maintenance cost, loss of cultural heritage, reduced lifespan of materials.
Adsorption by Activated Carbon
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Mechanism: Physical adsorption via van der Waals forces on highly porous carbon (surface area 500-1500 m²/g).
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Factors Affecting Capacity:
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Nature of adsorbate (polarity, molecular size).
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Temperature (decreases with increase).
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Carbon properties (surface area, pore size distribution).
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Process: Fixed-bed column. Breakthrough curve indicates when carbon needs regeneration.
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Regeneration: Thermal (steam/heat), chemical, or vacuum. Not 100% effective; carbon loses mass each cycle.
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Applications: Removal of VOCs, odours, taste/odor compounds, $$\displaystyle H_2S $$, residual chlorine, pesticides from air and water. Used in water treatment, air scrubbers, respirators.