Fractionation

Deethanizer Fundamentals

Ethane-propane separation in NGL fractionation per GPSA and industry practice.

Standards

GPSA Ch. 16 / GPA 2140

Industry standards for fractionation design and NGL product specifications.

Application

NGL Processing

Critical for separating ethane from the C3+ NGL product stream.

Priority

Product Spec

Essential for managing NGL vapor pressure and ethane purity.

Use this guide when you need to:

  • Size ethane recovery or rejection columns.
  • Calculate C2/C3 separation efficiency.
  • Manage column pressure and temperature profiles.
  • Troubleshoot reboiler and condenser duties.

1. Purpose and Position in NGL Fractionation

The deethanizer is a distillation column that separates ethane (C2) and lighter components from the propane-plus (C3+) NGL stream. It is a core unit in the NGL fractionation train, positioned after cryogenic recovery (turboexpander or cold box) and before the depropanizer.

Feed to the deethanizer is typically the C2+ bottom product from the demethanizer, or in some plant configurations, the raw NGL liquid directly from the cryogenic recovery section. The light key component is ethane (C2H6) and the heavy key component is propane (C3H8). The overhead product is an ethane-rich stream that may be sold as petrochemical feedstock or rejected to fuel gas, while the bottom product is the C3+ NGL that feeds the depropanizer.

NGL Fractionation Train Sequence

Column Top Product Bottom Product Key Separation
DemethanizerC1 (sales gas)C2+ (NGL)C1/C2
DeethanizerC2 (ethane)C3+ (NGL)C2/C3
DepropanizerC3 (propane)C4+C3/C4
DebutanizerC4 (butanes)C5+ (gasoline)C4/C5

The C2/C3 separation is one of the easier splits in the NGL train due to the relatively large difference in boiling points between ethane (−128°F) and propane (−44°F), resulting in favorable relative volatility. However, the column operates at elevated pressure and cryogenic overhead temperatures, which require refrigeration for the condenser.

2. Shortcut Column Design Method

The Fenske-Underwood-Gilliland (FUG) shortcut method provides a rapid preliminary estimate of minimum stages, minimum reflux, and actual stage count for a deethanizer column. While rigorous tray-by-tray simulation is required for final design, the FUG method is invaluable for screening studies and initial sizing.

Fenske Equation — Minimum Stages

The Fenske equation calculates the minimum number of theoretical stages at total reflux:

Nmin = ln[(xLK,D/xHK,D) × (xHK,B/xLK,B)] / ln(αavg)

Where:

  • Nmin = minimum number of theoretical stages
  • xLK,D, xHK,D = mole fractions of light key and heavy key in distillate
  • xLK,B, xHK,B = mole fractions of light key and heavy key in bottoms
  • αavg = geometric average relative volatility of light key to heavy key

Relative Volatility

Relative volatility is the ratio of equilibrium K-values for the light key and heavy key:

α = KLK / KHK = KC2 / KC3

For the C2/C3 separation, α typically ranges from 2.5 to 4.5 depending on pressure and temperature. The geometric average is taken between the top and bottom of the column: αavg = (αtop × αbottom)0.5. Higher α means easier separation and fewer stages.

Underwood Equation — Minimum Reflux

The Underwood equations determine the minimum reflux ratio (Rmin) at infinite stages. The method involves solving for the root θ from:

∑ [αi × xi,F / (αi − θ)] = 1 − q

Where q is the feed quality (q = 1 for saturated liquid, q = 0 for saturated vapor). Then the minimum reflux is obtained from:

Rmin + 1 = ∑ [αi × xi,D / (αi − θ)]

Gilliland Correlation

The Gilliland correlation relates the actual number of stages (N) to the actual reflux ratio (R) using the dimensionless variables X and Y:

X = (R − Rmin) / (R + 1)     Y = (N − Nmin) / (N + 1)

The Molokanov approximation of the Gilliland correlation gives:

Y = 1 − exp[(1 + 54.4X) / (11 + 117.2X) × (X − 1) / X0.5]

Typical design practice sets the actual reflux ratio at 1.1–1.3 times Rmin. The FUG method provides preliminary estimates; rigorous simulation (e.g., Aspen HYSYS, ProMax) is required for final design, particularly for multicomponent feeds.

3. Operating Pressure Selection

The operating pressure of the deethanizer determines the overhead temperature, which in turn dictates the type and cost of the condenser cooling system. Selecting the optimal pressure involves balancing separation efficiency against capital and operating costs.

Higher pressure raises the overhead temperature, making condensation easier and potentially allowing the use of less expensive cooling. However, higher pressure reduces the relative volatility between ethane and propane, requiring more trays and higher reflux.

Lower pressure improves relative volatility and separation efficiency (fewer trays, lower reflux), but results in colder overhead temperatures that demand propane refrigeration or other cryogenic cooling for the condenser.

Pressure vs. Overhead Temperature

Pressure (psig) Overhead Temp (°F) Condenser Coolant Relative α
350−30 to −10Propane refrigerationHigher
400−15 to 5Propane refrigerationModerate
4500 to 20Propane refrigerationLower
50010 to 35Mechanical refrigerationLowest

The economic tradeoff is significant: operating at lower pressure requires fewer trays (lower tower cost) but more expensive refrigeration (higher condenser cost and energy consumption). Most deethanizers in NGL plants operate in the 350–450 psig range, with propane refrigeration providing the condenser cooling. The optimal pressure is typically determined through a total-cost optimization study that considers column cost, condenser duty, refrigeration compressor power, and utility costs.

4. Tray Hydraulics and Column Diameter

Column diameter is determined by the vapor handling capacity, which is limited by the flooding velocity. The Souders-Brown correlation is the standard method for estimating the maximum allowable vapor velocity.

Souders-Brown Flooding Velocity

Uflood = CSB × [(ρL − ρV) / ρV]0.5

Where:

  • Uflood = flooding vapor velocity (ft/s)
  • CSB = Souders-Brown coefficient (ft/s), depends on tray spacing
  • ρL = liquid density (lb/ft³)
  • ρV = vapor density (lb/ft³)

CSB Factor by Tray Spacing

Tray Spacing (in) CSB (ft/s)
180.28
240.35
300.40

The design vapor velocity is typically set at 75–85% of the flooding velocity to provide adequate operating margin. The required column cross-sectional area is then:

Acolumn = V̇ / (Udesign)     where   Udesign = 0.80 × Uflood

Where V̇ is the volumetric vapor flow rate (ft³/s) at column conditions. The column inside diameter is then D = (4A/π)0.5, rounded up to the next standard vessel diameter.

Tray Types

  • Valve trays — Most common in deethanizer service; good efficiency over a wide operating range with turndown ratios of 3:1 to 5:1
  • Sieve trays — Lower cost but limited turndown (2:1); susceptible to weeping at low vapor rates
  • Bubble-cap trays — Excellent turndown but highest cost and pressure drop; used where zero liquid leakage is critical

Turndown is an important consideration for deethanizers because feed rates can vary significantly with upstream plant throughput changes. Valve trays are the most common choice for new deethanizer installations, offering the best balance of efficiency, cost, and flexibility.

5. Reboiler and Condenser Design

Condenser

The deethanizer condenser is typically a partial condenser, producing a vapor overhead product (ethane) and a liquid reflux stream. In some configurations, a total condenser is used when liquid ethane product is required (e.g., for pipeline shipment to an ethylene cracker).

The condenser duty is calculated from:

Qcond = V × λavg

Where V is the total overhead vapor rate (lb/hr) and λavg is the average latent heat of condensation (BTU/lb). Because the overhead temperature is typically −30 to +20°F depending on operating pressure, propane refrigeration is the most common cooling medium, with the refrigerant boiling at −40 to −20°F.

Reboiler

The reboiler duty for the deethanizer is approximately equal to the condenser duty plus feed preheat and heat losses (typically 10–15% additional):

Qreb ≈ Qcond + Qfeed + Qloss

The reboiler temperature depends on the bottoms composition and column pressure, typically ranging from 200 to 350°F. This is well within the range of hot oil, steam, or process-to-process heat exchange. The most common reboiler types for deethanizer service are:

  • Kettle reboiler — Most common for deethanizer service; provides good separation of vapor from liquid and handles varying heat loads well
  • Thermosiphon reboiler — Used when lower residence time is desired or when plot space is limited; requires adequate static head for natural circulation

For detailed reboiler sizing methodology, see the Reboiler Sizing Fundamentals guide.

Typical Duties by Feed Rate

Feed Rate (MBPD) Condenser Duty (MMBTU/hr) Reboiler Duty (MMBTU/hr)
108–1210–15
2520–3025–38
5040–6050–75
10080–120100–150

These values are approximate and depend strongly on feed composition, operating pressure, and product purity specifications. Detailed simulation is required for final engineering.

References

  1. GPSA, Chapter 16 — Hydrocarbon Recovery
  2. GPA Standard 2140 — Liquefied Petroleum Gas Specifications
  3. Kister, H.Z. — Distillation Design, McGraw-Hill
  4. ASME Boiler and Pressure Vessel Code, Section VIII, Division 1