Gas Dehydration

Silica Gel Dehydration

Design solid desiccant dehydration systems using silica gel, molecular sieves, or activated alumina with adsorption/regeneration cycles, bed sizing, breakthrough analysis, and comparison to glycol systems.

Silica gel design capacity

6-12 wt%

Dynamic capacity at operating conditions (100°F, 800 psia). Equilibrium capacity is higher (20-40%).

Achievable dew point

-40°F to -60°F

Silica gel typical. Molecular sieves achieve -100°F to -150°F for cryogenic applications.

Cycle time

8-24 hours

Adsorption: 8-24 hr. Regeneration: 2-4 hr heating + 2-3 hr cooling.

Use this guide when you need to:

  • Size silica gel or molecular sieve beds.
  • Design regeneration systems and cycles.
  • Compare solid desiccant vs TEG dehydration.

1. Overview & Applications

Solid desiccant dehydration uses porous materials (silica gel, molecular sieves, activated alumina) to adsorb water vapor from gas streams. Two or more beds operate in alternating adsorption/regeneration cycles to provide continuous dehydration.

Instrument air drying

Low dew point air

Silica gel or alumina dryers achieve -40°F to -100°F dew point for pneumatic controls.

Natural gas drying

Deep dehydration

Molecular sieves achieve < 1 ppmv water for cryogenic plants, LNG, ethylene.

Refrigerant drying

Prevent ice formation

Remove moisture from refrigeration loops to prevent freeze-up in cold heat exchangers.

Compressed air

Plant utility air

Dual-tower regenerative dryers for utility compressed air systems (150-200 psig).

Solid Desiccant vs Liquid Desiccant

Feature Solid Desiccant (Silica Gel, Mol Sieve) Liquid Desiccant (TEG, Glycol)
Outlet dew point -40°F to -150°F (mol sieve) -20°F to -60°F (TEG typical)
Typical applications Cryogenic plants, LNG, instrument air Sales gas, pipeline spec, moderate drying
Regeneration energy High (electric heaters, hot gas @ 400-600°F) Moderate (reboiler @ 350-400°F)
Capital cost Higher (multiple vessels, heaters, switching valves) Lower (single contactor, reboiler, pumps)
Operating cost Moderate (regeneration power, desiccant replacement) Moderate (fuel gas for reboiler, TEG losses)
Gas rate turndown Poor (fixed bed size, cycle time) Good (adjust circulation rate, reboiler duty)
Maintenance Desiccant replacement every 2-5 years, valve maintenance Glycol filters, pump seals, column trays

When to Use Solid Desiccant

  • Ultra-low dew point required: < -60°F (TEG cannot achieve this economically)
  • Upstream of cryogenic equipment: NGL fractionation, LNG liquefaction, ethylene plants
  • Small gas volumes: < 10 MMscfd where TEG system is oversized
  • Intermittent operation: Batch processes, startup/shutdown cycles
  • No liquid handling: Offshore platforms, remote locations where TEG logistics are difficult
Why silica gel vs molecular sieve: Silica gel is cheaper and suitable for moderate drying (-40°F dew point). Molecular sieves (3A, 4A, 5A zeolites) achieve deeper drying (-100°F to -150°F) but cost 3-5× more and require higher regeneration temperature (500-600°F vs 300-400°F for silica gel). Choose based on outlet dew point specification.

2. Adsorption Principles & Isotherms

Adsorption is the adhesion of water molecules to the pore surface of solid desiccant. Capacity depends on partial pressure of water (relative humidity) and temperature.

Adsorption Isotherms

Equilibrium Water Loading: q = f(P_H2O, T) Where: q = Water loading on desiccant (lb H₂O / lb desiccant) P_H2O = Partial pressure of water vapor (psia) T = Temperature (°F or K) Relative Humidity: RH = P_H2O / P_sat(T) × 100% Where P_sat(T) = Saturation vapor pressure of water at temperature T Desiccant capacity increases with relative humidity. Typical Isotherms (at 77°F): Silica gel (grade 01): RH = 10% → q = 0.08 (8 wt%) RH = 50% → q = 0.30 (30 wt%) RH = 90% → q = 0.40 (40 wt%) Molecular sieve 4A: RH = 10% → q = 0.15 (15 wt%) RH = 50% → q = 0.20 (20 wt%) RH = 90% → q = 0.22 (22 wt%) Note: Silica gel has steeper isotherm (capacity increases strongly with RH). Molecular sieve has flatter isotherm (capacity less sensitive to RH).

IMAGE: Adsorption Isotherms Comparison
Graph showing water loading (wt%) vs. relative humidity (%) for silica gel, molecular sieve 4A, and activated alumina at 77°F. Silica gel shows steep S-curve, molecular sieve shows flat plateau.

Breakthrough Curve

As gas flows through desiccant bed, water adsorbs near inlet forming a "mass transfer zone" (MTZ). This zone moves through bed over time until breakthrough occurs at outlet.

Breakthrough Time: t_break = (W_bed × q_eq × η_util) / (Q × y_in) Where: t_break = Time until outlet water concentration rises (hr) W_bed = Weight of desiccant in bed (lb) q_eq = Equilibrium loading capacity (lb H₂O / lb desiccant) η_util = Bed utilization factor (0.60-0.85 typical) Q = Gas flow rate (lb/hr) y_in = Inlet water concentration (lb H₂O / lb gas) Bed Utilization: η_util accounts for: - Mass transfer zone (MTZ) occupies portion of bed at breakthrough - Incomplete regeneration (heel water remains) - Non-uniform flow distribution Typical values: Silica gel: η = 0.70-0.80 Molecular sieve: η = 0.60-0.75 Activated alumina: η = 0.65-0.75 Lower utilization for: - High gas velocity (short residence time, wide MTZ) - Low temperature (slow kinetics) - Poor regeneration (high heel water)

IMAGE: Breakthrough Curve and Mass Transfer Zone
Two-part diagram: (1) Outlet water concentration vs. time showing S-curve breakthrough, (2) Cross-section of desiccant bed showing saturated zone, MTZ, and fresh desiccant zones with concentration profile.

Mass Transfer Zone (MTZ)

The MTZ is the region where water concentration transitions from inlet to outlet value:

  • Sharp MTZ: Fast kinetics, high mass transfer rate → thin zone → high bed utilization
  • Wide MTZ: Slow kinetics, low temperature, high velocity → thick zone → low utilization → larger bed required
  • MTZ length: Typically 1-3 ft for gas dehydration at normal conditions (100°F, 800 psia)

Adsorption Kinetics

Linear Driving Force (LDF) Model: dq/dt = k_s × (q_eq - q) Where: dq/dt = Rate of water adsorption (lb H₂O / lb desiccant / hr) k_s = Mass transfer coefficient (1/hr) q_eq = Equilibrium loading (from isotherm) q = Current loading Integration: q(t) = q_eq × (1 - exp(-k_s × t)) At equilibrium (t → ∞): q = q_eq Mass Transfer Coefficient: k_s = f(particle size, velocity, temperature, diffusivity) Smaller particles → larger k_s → faster kinetics → sharper MTZ Higher temperature → larger k_s → faster adsorption Higher velocity → thinner boundary layer → larger k_s Typical k_s values: 0.5-5.0 hr⁻¹ for natural gas dehydration

Effect of Temperature on Capacity

Higher temperature reduces adsorption capacity (exothermic process). Cool inlet gas improves performance:

Desiccant Capacity @ 77°F Capacity @ 150°F Capacity @ 250°F
Silica gel (RH=50%) 30 wt% 20 wt% 10 wt%
Molecular sieve 4A (RH=50%) 20 wt% 16 wt% 12 wt%
Activated alumina (RH=50%) 18 wt% 12 wt% 6 wt%
Inlet cooling benefit: Cooling gas from 120°F to 80°F before dehydration can increase desiccant capacity by 30-50%, reducing bed size or extending cycle time. Use inlet gas/gas heat exchanger or water-cooled trim cooler. Avoid cooling below hydrocarbon dew point to prevent liquid condensation in bed (fouls desiccant).

3. Desiccant Bed Design & Sizing

Bed Sizing Methodology

Step 1: Calculate Water Load to be Removed W_water = Q_gas × (y_in - y_out) × t_cycle Where: W_water = Total water adsorbed per cycle (lb) Q_gas = Gas flow rate (lb/hr) y_in = Inlet water content (lb H₂O / lb gas) y_out = Outlet water content (lb H₂O / lb gas) t_cycle = Adsorption time (hr) Convert to dew point using water vapor pressure charts: At 800 psia: 7 lb H₂O / MMscf → -20°F dew point 1 lb H₂O / MMscf → -60°F dew point 0.1 lb H₂O / MMscf → -100°F dew point Step 2: Calculate Required Desiccant Weight W_des = W_water / (q_eq × η_util) Where: q_eq = Equilibrium loading capacity (lb H₂O / lb desiccant) from isotherm η_util = Bed utilization factor (0.60-0.80) Step 3: Calculate Bed Volume V_bed = W_des / ρ_bulk Where: ρ_bulk = Bulk density of desiccant (lb/ft³) Silica gel: 45-50 lb/ft³ Molecular sieve 4A: 42-45 lb/ft³ Activated alumina: 52-58 lb/ft³ Step 4: Size Vessel Diameter (Limit Velocity) D = √(4 × Q_vol / (π × v_max)) Where: Q_vol = Volumetric flow rate at bed conditions (ft³/s) v_max = Maximum superficial velocity (ft/s) Horizontal flow: 20-40 ft/min (0.33-0.67 ft/s) Vertical upflow: 30-50 ft/min (avoid fluidization) Vertical downflow: 40-60 ft/min Step 5: Calculate Bed Height H = V_bed / A_cross Where A_cross = π D² / 4 Typical bed height: 6-15 ft (avoid excessive pressure drop or MTZ)

Pressure Drop Through Bed

Ergun Equation: ΔP/L = 150 × μ × v × (1-ε)² / (D_p² × ε³) + 1.75 × ρ × v² × (1-ε) / (D_p × ε³) Where: ΔP/L = Pressure drop per unit length (psi/ft) μ = Gas viscosity (lb/ft·s) v = Superficial velocity (ft/s) ε = Bed voidage (0.35-0.45 for spherical beads) D_p = Particle diameter (ft) ρ = Gas density (lb/ft³) First term = viscous (laminar) losses Second term = inertial (turbulent) losses Simplified for clean bed with 4-8 mesh beads (D_p = 0.01-0.02 ft): ΔP ≈ 0.2-0.5 psi per ft of bed height at v = 30 ft/min Design Limit: Total pressure drop < 10 psi (typical) If ΔP exceeds limit, increase vessel diameter to reduce velocity. Pressure drop increases with water loading (pores fill, ε decreases). Monitor ΔP during operation as indicator of bed saturation.

Example: Silica Gel Bed Sizing

Given: Gas flow rate: 10 MMscfd at 100°F, 800 psia Inlet dew point: +40°F @ 800 psia (y_in = 35 lb H₂O/MMscf) Outlet dew point: -40°F @ 800 psia (y_out = 3 lb H₂O/MMscf) Cycle time: 12 hours adsorption, 12 hours regeneration/cooling Desiccant: Silica gel, q_eq = 0.12 (12 wt%), η_util = 0.75 Solution: Gas mass flow (MW = 19, Z = 0.90): Q_gas = (10 MMscfd × 19 lb/lbmol) / (379 scf/lbmol) / 24 hr/day Q_gas = 20,850 lb/hr Water removal rate: W_water,rate = 20,850 lb/hr × (35 - 3) lb H₂O/MMscf / 10⁶ lb gas W_water,rate = 0.067 lb H₂O/hr Total water per cycle: W_water,cycle = 0.067 lb/hr × 12 hr = 0.80 lb H₂O Required desiccant weight: W_des = 0.80 / (0.12 × 0.75) = 8.9 lb This seems too small! Check calculation... Actually, convert MMscf to gas mass: 10 MMscfd = 10 × 10⁶ scf/day / 24 hr = 417,000 scf/hr Mass = 417,000 scf/hr × 19 lb/379 scf = 20,900 lb/hr ✓ Water content: 35 lb/MMscf = 35 lb H₂O per 10⁶ scf = 35 × 19 lb gas / 379 scf / 10⁶ scf = 1,750 ppmw (parts per million weight) Revised: y_in = 1750 ppmw = 0.00175 lb H₂O/lb gas y_out = 175 ppmw = 0.000175 lb H₂O/lb gas W_water,rate = 20,900 × (0.00175 - 0.000175) = 32.9 lb H₂O/hr W_water,cycle = 32.9 × 12 = 395 lb H₂O per cycle W_des = 395 / (0.12 × 0.75) = 4,390 lb silica gel Bed volume: V_bed = 4,390 lb / 48 lb/ft³ = 91 ft³ Vessel sizing (limit v < 40 ft/min): Gas volume at bed conditions (100°F, 800 psia): Q_vol = 417,000 scf/hr × (14.7/800) × ((100+460)/(60+520)) = 12,600 acfh = 3.5 acfs A_cross = 3.5 ft³/s / (40 ft/min / 60 s/min) = 5.25 ft² D = √(4 × 5.25 / π) = 2.6 ft → Use 3 ft ID vessel Bed height: H = 91 ft³ / (π × 1.5² ft²) = 12.9 ft → Use 13 ft bed height Pressure drop (estimate): ΔP ≈ 0.3 psi/ft × 13 ft = 3.9 psi (acceptable) Final Design: Two vessels: 3 ft ID × 20 ft T-T (13 ft bed, 7 ft freeboard/inlet diffuser) Desiccant charge: 4,400 lb silica gel per vessel Cycle: 12 hr online, 12 hr offline (regeneration + cooling)

Vessel Internals

  • Inlet diffuser: Distribute gas uniformly across bed cross-section (perforated pipe, bubble cap tray)
  • Support grid: Hold desiccant while allowing gas flow (wedge wire screen, Johnson screen, ceramic balls)
  • Hold-down grid: Prevent fluidization during high-velocity regeneration (top of bed)
  • Outlet collector: Collect dried gas without entraining fines (internal piping, nozzle screens)
  • Thermowells: Monitor bed temperature during adsorption/regeneration (top, middle, bottom locations)

IMAGE: Desiccant Vessel Cross-Section
Cutaway diagram showing vessel internals: inlet distributor at top, hold-down screen, desiccant bed with thermowell locations (top/mid/bottom), support screen, ceramic ball layer, and outlet collector piping.

Design margins: Add 20-30% desiccant capacity margin for degradation over time, seasonal variations in inlet humidity, and process upsets. Use minimum 2 beds (one online, one regenerating) or 3 beds for continuous operation with staggered cycles. Size vessels for pressure/temperature during regeneration (typically 250-600°F, full operating pressure).

4. Regeneration Cycles & Heating Methods

Regeneration removes adsorbed water by heating desiccant to reverse adsorption equilibrium. Hot gas (or electric heaters) desorbs water, which is vented or condensed.

Regeneration Methods

Method Heating Source Temperature Applications
Hot gas regeneration Heated process gas or dry regeneration gas 300-600°F Large natural gas dehydration, continuous operation
Electric heater Immersion heaters or external heater + blower 350-450°F Instrument air dryers, small skid packages
Steam heating Steam coils in bed or jacketed vessel 250-350°F Where steam available (refineries, plants with boilers)
Depressurization (PSA) Pressure swing adsorption, no external heat Ambient Low-pressure applications, hydrogen purification

IMAGE: Two-Bed Solid Desiccant Dehydration System P&ID
Process flow diagram showing two parallel vessels with switching valves, heater, cooler/condenser, and regeneration gas loop. One bed on adsorption (wet gas in, dry gas out), other on regeneration (hot gas flow).

Hot Gas Regeneration Design

Regeneration Heat Requirement: Q_regen = Q_sensible + Q_desorption + Q_vaporization + Q_loss Where: Q_sensible = Heat desiccant from T_ads to T_regen = W_des × Cp_des × (T_regen - T_ads) Cp_des ≈ 0.20 Btu/lb·°F for silica gel and molecular sieves Q_desorption = Heat of desorption (release adsorbed water) = W_water × ΔH_ads ΔH_ads ≈ 1800 Btu/lb H₂O for silica gel ΔH_ads ≈ 1900 Btu/lb H₂O for molecular sieve Q_vaporization = Vaporize liquid water = W_water × λ λ = 1050 Btu/lb (latent heat of water at ~250°F) Q_loss = Heat loss through vessel walls = U × A_vessel × (T_regen - T_amb) × t_regen Typically Q_loss = 5-15% of total regeneration duty Example (from previous silica gel bed): W_des = 4,390 lb W_water = 395 lb H₂O per cycle T_ads = 100°F (adsorption) T_regen = 400°F (regeneration) t_regen = 4 hours Q_sensible = 4,390 × 0.20 × (400-100) = 263,000 Btu Q_desorption = 395 × 1800 = 711,000 Btu Q_vaporization = 395 × 1050 = 415,000 Btu Q_loss = 10% of sum ≈ 139,000 Btu Q_total = 1,528,000 Btu over 4 hours Heat rate = 1,528,000 / 4 = 382,000 Btu/hr = 112 kW If using electric heaters: 112 kW × 4 hr × $0.08/kWh = $36 per cycle

Regeneration Gas Flow Rate

Minimum Gas Flow (Heat Transfer Limited): m_gas = Q_regen / (Cp_gas × ΔT) Where: Q_regen = Heat duty (Btu/hr) Cp_gas = Gas heat capacity (Btu/lb·°F) ≈ 0.5 for natural gas ΔT = Gas cooling across bed (°F) Example: Q_regen = 382,000 Btu/hr ΔT = 100°F (gas enters at 450°F, exits at 350°F) m_gas = 382,000 / (0.5 × 100) = 7,640 lb/hr Convert to volumetric flow (at 400°F avg, 800 psia): Q_vol = 7,640 lb/hr × 379 scf / (19 lb/lbmol) × (460+400)/520 × 14.7/800 Q_vol = 6,100 scfh = 0.15 MMscfd Minimum Gas Flow (Mass Transfer Limited): Must also remove water vapor from bed Maximum water content in regeneration gas ≈ 1000-5000 ppmv (avoid condensation in cooler) m_gas,min = W_water / (t_regen × y_max) Where y_max = max allowable water loading in regen gas If y_max = 0.02 lb H₂O/lb gas (2 wt%): m_gas,min = 395 lb / (4 hr × 0.02) = 4,940 lb/hr Use larger of heat-limited or mass-limited flow rate. Typical regen gas rate = 3-10% of process gas rate.

Regeneration Cycle Steps

  1. Depressurization (0.5-1 hr): Close inlet valve, slowly vent vessel to regeneration pressure (atmospheric or 50-100 psig for closed-loop). Slow vent prevents bed cooling (adiabatic expansion) and fines carryover.
  2. Heating (2-4 hr): Circulate hot gas (counter-current to adsorption flow) to heat bed and desorb water. Monitor outlet temperature – when T_out approaches T_in, bed is heated.
  3. Cooling (2-4 hr): Circulate ambient or cooled gas to reduce bed temperature to < 120°F before repressurization. High temperature + rapid pressurization can damage desiccant.
  4. Repressurization (0.5-1 hr): Slowly pressurize with dry process gas to operating pressure. Too-fast pressurization can fluidize bed, break beads, generate fines.
  5. Online (adsorption): Resume normal flow, monitor outlet dew point for breakthrough.

Regeneration Gas Sources

Option 1: Slip Stream of Process Gas

Take 5-10% of dry outlet gas, heat with fired heater or electric heater, use for regeneration:

  • Pros: Simple, dry gas already available
  • Cons: Loss of product gas (vented or flared with water vapor)

Option 2: Closed-Loop Regeneration Gas

Use dedicated blower to circulate regeneration gas through heater → bed → cooler/condenser → blower:

  • Pros: No loss of process gas, better heat efficiency
  • Cons: More complex, requires blower, condenser to remove water

Option 3: External Heating (Steam, Hot Oil)

Jacket vessel or install internal coils with steam or hot oil:

  • Pros: No regeneration gas required
  • Cons: Slower heat transfer, risk of local overheating, requires steam/hot oil system
Regeneration best practices: Use counter-current heating (opposite direction to adsorption flow) to push desorbed water out inlet end where it's already saturated. Limit heating rate to < 50°F/hr to prevent thermal shock and desiccant cracking. Cool bed to < 120°F before repressurization. Monitor bed temperature with thermocouples at top/middle/bottom to verify complete heating and cooling.

5. Desiccant Types & Selection

Comprehensive Comparison

Property Silica Gel Molecular Sieve 3A/4A Activated Alumina
Chemical formula SiO₂·nH₂O (amorphous) Zeolite (crystalline aluminosilicate) Al₂O₃ (gamma-alumina)
Typical particle size 4-8 mesh (2-5 mm) 4-8 mesh, 8-12 mesh 4-8 mesh
Bulk density 45-50 lb/ft³ 42-45 lb/ft³ 52-58 lb/ft³
BET surface area 600-800 m²/g 700-900 m²/g 200-300 m²/g
Pore size 20-50 Å (mesoporous) 3-4 Å (microporous, uniform) 20-100 Å (mesoporous)
Equilibrium capacity (@ 50% RH, 77°F) 28-35 wt% 18-22 wt% 16-20 wt%
Typical outlet dew point -40°F to -60°F -100°F to -150°F -40°F to -80°F
Regeneration temperature 300-400°F 450-600°F 350-450°F
Cost (relative) 1.0× (baseline) 3-5× (expensive) 1.5-2.5×
Typical service life 2-4 years 3-5 years 3-5 years
Attrition resistance Good (hard beads) Fair (can generate fines) Excellent (very hard)
Liquid water tolerance Poor (can crack) Very poor (can disintegrate) Fair

Molecular Sieve Types

Zeolite molecular sieves are categorized by pore diameter:

  • Type 3A (3 Ångstrom pore): Adsorbs water (2.6 Å) but excludes ethane (3.8 Å) and larger. Used when must not adsorb hydrocarbons (ethylene drying, natural gas with no HC adsorption).
  • Type 4A (4 Ångstrom pore): Adsorbs water, methane, ethane. Most common for natural gas dehydration. Higher capacity than 3A for water.
  • Type 5A (5 Ångstrom pore): Adsorbs water, C1-C4 hydrocarbons. Used for sweetening (H₂S/CO₂ removal) and drying in one step.
  • Type 13X (10 Ångstrom pore): Large pore, adsorbs aromatics, mercaptans. Used for liquid treating, not gas drying.

When to Use Each Desiccant

Use Silica Gel When:

  • Outlet dew point -40°F to -60°F is acceptable
  • Moderate gas flow rates (not ultra-low dew point requirement)
  • Cost is primary concern (lowest initial cost)
  • Applications: Instrument air drying, natural gas to -40°F, refrigerant drying

Use Molecular Sieve When:

  • Deep dehydration required (< -80°F dew point, < 1 ppmv water)
  • Upstream of cryogenic equipment (LNG, ethylene, NGL fractionation)
  • High reliability and long service life justify higher cost
  • Applications: LNG feed gas, gas plant feed, ethylene cracker feed, fuel gas to gas turbines

Use Activated Alumina When:

  • Moderate dew point (-60°F to -80°F)
  • High mechanical strength needed (high-velocity applications)
  • Liquid water slugs possible (more forgiving than silica gel or mol sieve)
  • Applications: Compressed air dryers, natural gas moderate drying, acid gas drying

Desiccant Degradation & Replacement

Desiccants degrade over time due to:

  • Liquid water slugs: Rapid adsorption releases heat → thermal shock → cracking/disintegration
  • Liquid hydrocarbon contamination: Coats pore surface, blocks adsorption sites, difficult to regenerate
  • Compressor oil carryover: Fouls bed, reduces capacity (install coalescing filters upstream)
  • Fines generation: Attrition from thermal cycling, high velocity, vibration → plugs downstream screens
  • Irreversible adsorption: Heavy hydrocarbons, glycol, amines adsorb and don't desorb → permanent capacity loss

Signs Desiccant Replacement is Needed

  1. Breakthrough occurs earlier than design (shorter cycle time)
  2. Outlet dew point rises above specification
  3. Pressure drop increases significantly (fines accumulation, bed compaction)
  4. Visual inspection shows color change (contamination), cracking, or dust (fines)
  5. Typical replacement interval: 2-5 years depending on service severity
Selection summary: For -40°F dew point, use silica gel (lowest cost). For -80°F to -100°F, use molecular sieve 4A (industry standard for cryogenic gas plants). For liquid water exposure risk, use activated alumina (most robust). Always install inlet separator to remove free liquids, inlet filter to remove particulates, and monitor outlet dew point continuously to detect early breakthrough.