Introduction to Chemical Engineering
Chemical engineering is the branch of engineering that applies physical sciences (physics and chemistry), life sciences (microbiology and biochemistry), together with mathematics and economics to produce, transform, transport, and properly use chemicals, materials and energy. It combines the knowledge of chemistry, physics, biology, and mathematics to solve problems related to the production or use of chemicals on an industrial scale.
Fundamental Concepts & Units
SI Units and Conversions
| Physical Quantity | SI Unit | Common Conversions |
|---|---|---|
| Mass | kg | 1 kg = 2.205 lb |
| Length | m | 1 m = 3.281 ft |
| Time | s | 1 hr = 3600 s |
| Temperature | K | K = °C + 273.15, °F = (9/5)°C + 32 |
| Pressure | Pa | 1 atm = 101,325 Pa = 14.696 psi |
| Energy | J | 1 cal = 4.184 J, 1 BTU = 1055 J |
| Power | W | 1 hp = 745.7 W |
| Volume | m³ | 1 m³ = 1000 L = 264.2 gal (US) |
| Viscosity (dynamic) | Pa·s | 1 Pa·s = 10 Poise |
| Viscosity (kinematic) | m²/s | 1 m²/s = 10⁴ centistokes |
Dimensional Analysis
Step-by-step process:
- Identify known quantities and target units
- Write conversion factors as fractions
- Multiply by conversion factors so units cancel
- Calculate final value
Example: Convert 55 mph to m/s 55 (miles/hour) × (1609 m/mile) × (1 hour/3600 s) = 24.7 m/s
Thermodynamics
Laws of Thermodynamics
First Law (Conservation of Energy): Energy can neither be created nor destroyed, only transferred or converted
- ΔU = Q – W
- ΔU = change in internal energy
- Q = heat added to system
- W = work done by system
Second Law: The entropy of an isolated system always increases
- ΔS ≥ 0 (for isolated systems)
- ΔS = Q/T (for reversible processes)
Third Law: As temperature approaches absolute zero, entropy approaches a minimum value
Thermodynamic Properties
Enthalpy (H)
- H = U + PV
- ΔH = ΔU + Δ(PV)
- For constant pressure: ΔH = Q_p
Entropy (S)
- dS = δQ_rev/T
- ΔS = ∫(δQ_rev/T)
- For ideal gas: ΔS = C_p·ln(T₂/T₁) – R·ln(P₂/P₁)
Gibbs Free Energy (G)
- G = H – TS
- ΔG = ΔH – TΔS
- At equilibrium: ΔG = 0
- For spontaneous reaction: ΔG < 0
Equations of State
Ideal Gas Law
- PV = nRT
- P = pressure (Pa)
- V = volume (m³)
- n = moles
- R = gas constant (8.314 J/mol·K)
- T = temperature (K)
Van der Waals Equation
- (P + a(n/V)²)(V-nb) = nRT
- a = attractive parameter
- b = volume parameter
Virial Equation
- PV/nRT = 1 + B/V + C/V² + …
- B, C = virial coefficients
Compressibility Factor
- Z = PV/nRT
- For ideal gas: Z = 1
Fluid Mechanics
Fluid Statics
Pressure Variation with Height
- ΔP = ρgΔh
- ρ = fluid density
- g = gravitational acceleration
- Δh = height difference
Hydrostatic Force on a Submerged Surface
- F = ρgh_c A
- h_c = depth to centroid
- A = surface area
Fluid Dynamics
Bernoulli’s Equation
- P₁ + ½ρv₁² + ρgh₁ = P₂ + ½ρv₂² + ρgh₂
- P = pressure
- v = velocity
- h = height
Continuity Equation
- ṁ = ρ₁A₁v₁ = ρ₂A₂v₂
- ṁ = mass flow rate
- A = cross-sectional area
Reynolds Number
- Re = ρvD/μ = vD/ν
- D = characteristic length
- μ = dynamic viscosity
- ν = kinematic viscosity
Flow Regimes:
- Re < 2300: Laminar flow
- 2300 < Re < 4000: Transitional
- Re > 4000: Turbulent flow
Pumps and Pipelines
Energy Balance in Pipe Systems
- (P₁/ρg + v₁²/2g + z₁) + hₚ = (P₂/ρg + v₂²/2g + z₂) + hᴌ
- hₚ = pump head
- hᴌ = head loss
Friction Factor and Head Loss
- For laminar flow: f = 64/Re
- For turbulent flow: 1/√f = -2log(ε/3.7D + 2.51/Re·√f) (Colebrook equation)
- Head loss: hᴌ = f(L/D)(v²/2g)
- ε = pipe roughness
- L = pipe length
Pump Power
- P = ρgQH/η
- Q = volumetric flow rate
- H = pump head
- η = pump efficiency
Heat Transfer
Modes of Heat Transfer
Conduction
- q = -kA(dT/dx)
- q = heat transfer rate (W)
- k = thermal conductivity (W/m·K)
- A = cross-sectional area (m²)
- dT/dx = temperature gradient (K/m)
Convection
- q = hA(Ts – T∞)
- h = convective heat transfer coefficient (W/m²·K)
- Ts = surface temperature
- T∞ = fluid temperature
Radiation
- q = εσA(Ts⁴ – Tsurr⁴)
- ε = emissivity
- σ = Stefan-Boltzmann constant (5.67 × 10⁻⁸ W/m²·K⁴)
- Tsurr = surrounding temperature
Heat Exchangers
Logarithmic Mean Temperature Difference (LMTD)
- LMTD = (ΔT₁ – ΔT₂)/ln(ΔT₁/ΔT₂)
- For counter-flow: ΔT₁ = Th,in – Tc,out, ΔT₂ = Th,out – Tc,in
- For parallel flow: ΔT₁ = Th,in – Tc,in, ΔT₂ = Th,out – Tc,out
Heat Transfer Rate
- Q = UA·LMTD
- U = overall heat transfer coefficient
- A = heat transfer area
Effectiveness-NTU Method
- ε = actual heat transfer / maximum possible heat transfer
- NTU = UA/Cmin
- Cmin = (ṁcp)min
Mass Transfer
Fick’s Laws of Diffusion
First Law (Steady State)
- J = -D(dC/dx)
- J = diffusion flux (mol/m²·s)
- D = diffusion coefficient (m²/s)
- dC/dx = concentration gradient (mol/m⁴)
Second Law (Unsteady State)
- dC/dt = D(d²C/dx²)
Mass Transfer Coefficients
- NA = kc(CA,s – CA,∞)
- NA = mass transfer rate of A
- kc = mass transfer coefficient
- CA,s = concentration at surface
- CA,∞ = concentration in bulk fluid
Dimensionless Numbers
- Schmidt Number: Sc = μ/ρD
- Sherwood Number: Sh = kcL/D
- Peclet Number: Pe = vL/D
Reaction Engineering
Reaction Rate
- rA = -dCA/dt = k·f(CA, CB, …)
- k = rate constant
- f() = function of concentrations
Arrhenius Equation
- k = A·e^(-Ea/RT)
- A = pre-exponential factor
- Ea = activation energy
- R = gas constant
- T = absolute temperature
Reactor Design Equations
Batch Reactor
- dCA/dt = rA
- t = ∫(dCA/rA) from CA0 to CA
Continuous Stirred Tank Reactor (CSTR)
- V = FA0(XA)/(-rA)
- V = reactor volume
- FA0 = molar flow rate of A
- XA = conversion of A
Plug Flow Reactor (PFR)
- V = FA0∫(dXA/(-rA)) from 0 to XA
- dV/dXA = FA0/(-rA)
Catalysis
- Rate = k·[catalyst]·f(reactants)
- Catalyst lowers activation energy without being consumed
Separation Processes
Distillation
Relative Volatility
- α = (yA/xA)/(yB/xB)
- yA, yB = vapor phase compositions
- xA, xB = liquid phase compositions
McCabe-Thiele Method
- Operating lines: y = (L/V)x + (F/V)
- L = liquid flow rate
- V = vapor flow rate
- F = feed flow rate
Minimum Reflux Ratio
- (L/D)min = xD(1-xF)/(xF(1-xD))
- xD = distillate composition
- xF = feed composition
Extraction
Distribution Coefficient
- KD = concentration in extract / concentration in raffinate
Number of Stages
- For countercurrent extraction with constant KD:
- N = ln[(Rout – mSin)/(Rin – mSin)]/ln[(L + mV)/L]
- R = raffinate concentration
- S = solvent concentration
- m = distribution coefficient
- L, V = flow rates
Absorption/Stripping
Height of a Transfer Unit (HTU)
- HTU = L/KLa or V/KGa
- KLa, KGa = volumetric mass transfer coefficients
Number of Transfer Units (NTU)
- NTU = ∫(dx/(y* – y)) from bottom to top
- y* = equilibrium vapor composition
Process Control
Transfer Functions
First-order System
- G(s) = K/(τs + 1)
- K = gain
- τ = time constant
Second-order System
- G(s) = K/(τ²s² + 2ζτs + 1)
- ζ = damping coefficient
PID Controllers
Controller Equation
- u(t) = Kp·e(t) + Ki∫e(t)dt + Kd·de(t)/dt
- u(t) = controller output
- e(t) = error = setpoint – measured value
- Kp = proportional gain
- Ki = integral gain
- Kd = derivative gain
Tuning Methods
Ziegler-Nichols Method:
| Controller | Kp | Ti | Td |
|---|---|---|---|
| P | 0.5Ku | – | – |
| PI | 0.45Ku | Pu/1.2 | – |
| PID | 0.6Ku | Pu/2 | Pu/8 |
- Ku = ultimate gain
- Pu = ultimate period
Process Design & Economics
Capital Cost Estimation
Six-Tenths Rule
- Cost₂ = Cost₁(Size₂/Size₁)^0.6
Lang Factor
- Fixed capital investment = Σ(equipment costs) × Lang factor
- For solid processing plants: Lang factor ≈ 3.1
- For fluid processing plants: Lang factor ≈ 4.7
- For mixed processing plants: Lang factor ≈ 3.6
Operating Cost Estimation
Manufacturing Costs
- Direct production costs
- Fixed charges
- Plant overhead costs
- General expenses
Profitability Analysis
- Payback period = Total capital investment / Annual cash flow
- Return on investment (ROI) = (Annual profit / Total capital investment) × 100%
- Net present value (NPV) = Σ[CFt/(1+r)^t] – Initial investment
- Internal rate of return (IRR): r when NPV = 0
Safety & Environmental
Hazard Analysis
HAZOP (Hazard and Operability Study)
- Systematic examination of process deviations
- Guide words: No, More, Less, As Well As, Part Of, Reverse, Other Than
Risk Assessment Matrix
- Likelihood × Consequence = Risk level
Emission Control
Air Pollution Control Efficiency
- Efficiency = (inlet concentration – outlet concentration) / inlet concentration × 100%
Wastewater Treatment Parameters
- BOD (Biochemical Oxygen Demand)
- COD (Chemical Oxygen Demand)
- TOC (Total Organic Carbon)
- TSS (Total Suspended Solids)
Common Chemical Processes
Petrochemicals
- Crude oil distillation
- Catalytic cracking
- Reforming
- Alkylation
Polymers
- Addition polymerization
- Condensation polymerization
- Injection molding
- Extrusion
Biochemical
- Fermentation
- Enzymatic reactions
- Bioreactors
- Downstream processing (filtration, chromatography)
Resources for Further Learning
Professional Organizations
- American Institute of Chemical Engineers (AIChE)
- Institution of Chemical Engineers (IChemE)
- Society of Chemical Industry (SCI)
Key Reference Books
- Perry’s Chemical Engineers’ Handbook
- Coulson and Richardson’s Chemical Engineering
- Unit Operations of Chemical Engineering (McCabe)
- Chemical Process Safety (Crowl and Louvar)
Online Resources
- National Institute of Standards and Technology (NIST)
- Chemical Engineering World
- MIT OpenCourseWare – Chemical Engineering
- Process Engineering Associates Technical Resources
This cheatsheet provides a comprehensive reference for chemical engineering fundamentals. Always verify calculations and consult detailed references for specific applications.
