A look into flare gas: 50–70% methane, nearly half convertible into solid carbon instead of emissions.
Average Associated/Flare Gas Composition
The gas that ends up in a flare stack is usually associated gas (from oil wells) or waste gas from processing units. It’s highly variable by basin, but industry data shows typical ranges:
- Methane (CH₄): 40–70%
- Ethane (C₂H₆): 5–15%
- Propane (C₃H₈): 2–8%
- Butanes & heavier (C₄+): 1–8%
- Carbon dioxide (CO₂): 1–10%
- Nitrogen (N₂): 0.5–5%
- Hydrogen sulfide (H₂S): trace to 5% (sour gas fields)
- Other inerts (argon, water vapor, etc.): <1%
👉 In practice: A “lean” gas is ~80–90% methane. A “rich” gas can be closer to 50–60% methane with heavier hydrocarbons mixed in.
What the Gas Leaving a Flare Looks Like
When gas is flared:
- Ideally, it burns completely → mainly CO₂ + H₂O.
- In reality, combustion is often incomplete → you’ll see:
- CO₂ (70–90% of exhaust)
- H₂O vapor (5–15%)
- Unburnt CH₄ (0.5–5%)
- CO (1–5%)
- NOₓ, SOₓ, soot (traces)
So the flare plume is mostly hot CO₂ and steam with small but critical amounts of unburnt methane (high GWP greenhouse gas).
How Much of Flared Gas Is Methane (Unburned)?
Studies show flare combustion efficiency ranges 92–98%. That means:
- If your incoming gas is ~60% methane, then only ~1–5% of that methane slips unburnt through the flame.
- Example: Gas stream = 60% CH₄, 100 MSCFD. After flare: 92% burned → ~55 MSCFD methane destroyed, ~5 MSCFD slips through.
How Much Carbon Can Be Captured (via Pyrolysis)
Methane pyrolysis reaction:
CH4→C(solid)+2H2CH₄ → C (solid) + 2 H₂CH4→C(solid)+2H2
- 1 mole CH₄ (16 g) → 1 mole carbon (12 g) + 2 moles H₂ (4 g).
- So 75% of methane’s mass can become solid carbon, and 25% becomes hydrogen.
👉 In percentage terms:
- From the methane fraction only: up to 75% of its weight becomes usable solid carbon.
- If flare gas is ~60% methane, then roughly 45% of the entire gas stream’s mass could be carbonized (the rest being hydrogen, CO₂, inerts, heavier hydrocarbons).
Is composition predictable?
- Within one asset: Somewhat. A single separator or plant train tends to swing inside a band (e.g., “lean” vs “rich” days), but turnarounds, well changes, and upset routing cause step-changes.
- Across sites & flare events: Not very. Different fields, liquids loading, and emergency flares = bigger swings (heavies, CO₂, H₂S, N₂, water).
Why it matters for pyrolysis (and any H₂/C recovery)
- Heating value & Wobbe swings: change reactor duty, residence time, and carbon morphology.
- Heavies (C₂+): raise coke/soot rates; can plug or foul.
- CO₂/N₂/H₂O (diluents): lower partial pressure of CH₄ → lower throughput per kW.
- H₂S/mercaptans: poisoning/corrosion; sulfur-contaminated carbon product.
- Water & aerosols: quench hot zones, cause thermal shock.
- Oxygen ingress (rare but during upsets): safety hazard in hot reactors.
Practical approach (pre-process)
- Inline gas analysis: micro-GC + TDL/IR for CO₂/H₂S + dew-point meter. Aim for 30–120s refresh.
- Feed conditioning:
- Knockout + coalescer + heat tracing (remove liquids/water).
- Desulfurization (ZnO bed or amine slipstream) if H₂S > product spec.
- Optional CO₂ trim only if it crushes capacity; not always required.
- Buffering & blending: small surge vessel to smooth short spikes; blend rich + lean sources when possible.
Reactor control (real-time)
- Closed-loop duty control: adjust wall temperature/power to hit target CH₄ conversion at measured CH₄%.
- Residence-time control: modulate flow to keep Damköhler number in spec.
- Anti-foul strategy: periodic thermal pulses or nitrogen sweeps; staged reactors for isolation/cleaning.
- Set “operating envelopes”: define safe/efficient windows for CH₄%, H₂S ppm, dew point; auto-derate or bypass outside limits.
Post-process “tackle plan”
- Hydrogen train: membranes → PSA; adjust cut based on measured diluents to keep purity ≥ spec.
- Carbon handling: cyclone + filter; de-ashing/desulfurization if needed; granulate/briquette to stable SKUs; QC for sulfur, surface area, and color.
- Sulfur management: regenerate ZnO/amine; consider sulfur recovery if volumes justify.
- Analytics & QA: batch-tag carbon lots with feed gas assays; sell high-spec lots premium, down-spec to industrial uses.
- Fallback modes: when composition goes out of envelope, divert to flare or thermal oxidizer and resume when stable—protects equipment and product brand.
Data/controls layer
- Soft sensors / “virtual analyzer”: ML model maps analyzer + process signals → predicted CH₄% and foul rate; pre-emptive setpoint moves.
- Run rules: site-specific recipes (e.g., “Basin A rich gas: +20°C wall temp, –10% flow”).
- SLA language with operators: define minimum CH₄%, max H₂S, dew point, and notification timelines; price in a variability fee.
Bottom line
Composition will vary more than you think during real-world flaring. Design for it: measure fast, precondition smart, control tightly, and grade product after.
Future option
There is active research on plasma and photochemical H₂S splitting (aimed at producing green H₂ from sour gas fields). If you’re building modular flare-gas units, you could someday bolt on an H₂S-to-H₂ + S₂ module. But today it’s still lab/early pilot scale—not bankable like amine + Claus.
Design basis (assumptions)
- Flow: 0.25 MMSCFD (~10,400 scfh ≈ 295 Nm³/h)
- Pressure available to contactor: 80–150 psig
- Temp: 20–40 °C (heated/traced to avoid condensation)
- Composition envelope: CH₄-rich gas with H₂S 0.5–2.0 mol%, CO₂ variable; target <4 ppmv H₂S to protect pyrolysis & carbon quality
- Solvent: 40 wt% MDEA (selective for H₂S; let most CO₂ slip)
What that sizes to (practical, not lab-perfect)
Amine circulation (lean → rich Δloading ≈ 0.33 mol/mol):
- Theoretical need at 0.5–2.0% H₂S: ~0.3–1.0 gpm
- Reality: hydraulics, control stability, and swings demand a minimum.
- Specify: 3–5 gpm design circulation (gives you ~3–10× headroom for spikes and easy turndown).
Contactor (absorber):
- 8–10 in. diameter, 10–15 ft packed height (structured packing), ANSI 150/300
- Mist eliminator + coalescer upstream
Regenerator (stripper) + reboiler:
- 6–8 in. diameter, 10–14 ft packed trays/packing
- Reboiler duty: ~75–150 kW (0.25–0.5 MMBtu/h) at 3–5 gpm circulation
- Lean/rich exchanger (plate & frame), air cooler or small water cooler
Tanks & ancillaries:
- Lean/rich surge: 0.5–1.0 m³ each
- Solvent inventory: ~1–2 m³ total
- Knockout + coalescer + electric heat tracing on inlet
- Optional: slipstream ZnO guard if sour spikes exceed spec
Controls:
- PID on circulation, reboiler duty, and regenerator overhead temp
- H₂S analyzer (inlet/outlet), dew point, and differential pressure (packing health)
Turndown & swings:
- Stable 3:1–4:1 turndown at spec with this sizing
- Add a 2–5 min gas surge vessel (ASME) before the contactor to smooth flare slugs
Skid & footprint options (how small can we go?)
Single-skid “micro” package (tight sites):
- Target footprint: 10–12 ft L × 4–6 ft W × 9–10 ft H
- What’s on it: contactor, pumps, exchangers, small reboiler (electric or NG-fired), controls, cable tray
- Trade-offs: tighter maintenance access; regenerator column height may require a fold-down or removable stack
Standard 20-ft ISO modular (most practical):
- Two short skids that bolt together or a single 20-ft frame
- Full access, better noise/heat management, easy trucking & craning
- Easiest path to adding a ZnO guard or bigger reboiler later
Ultra-compact 10-ft skid?
- Possible if you outboard the reboiler (separate cube) and accept tighter service clearances
- Works for steady, cleaner gas; less forgiving for big upset swings
Indicative CAPEX & utilities (budgetary)
- New, small modular (3–5 gpm): US$650k–$1.1M all-in (mechanical + controls; install & utilities excluded)
- Refurb/used packages: US$300k–$700k depending on condition & metallurgy
- Power/heat: 75–150 kW reboiler duty (electric or NG), 3–7 kW pumps & controls
- Chemicals: initial 1–2 m³ MDEA solution; small annual makeup
Why this works for your pyrolysis train
- Keeps H₂S → <4 ppm (protects carbon value & downstream metallurgy)
- Lets CO₂ slip, preserving energy efficiency and simplicity
- Sized for control stability (not just stoichiometry), so you can ride flare-event variability without tripping the unit
- Modular path: start with the micro-train, bolt on a larger reboiler or ZnO guard if your basin turns out spikier than expected