A Technical Primer on Hydrocarbon Extraction

Every figure here comes from N.B. Oler design data, system specifications and in-house testing. No industry averages.

DocumentTechnical Brief 10
Issued byN.B. Oler, LLC
Revision2026.1
Issued17 September 2026
Light hydrocarbons are non-polar. Cannabinoids and terpenes are non-polar. Chlorophyll, sugars, salts and most of the water in your biomass are polar. That single fact is the whole argument for hydrocarbon extraction: the solvent picks up what you want and leaves a large share of what you do not, before you have filtered anything.

01. Why butane and propane

Solvent Boiling point at 1 atm What it buys you
n-Butane -1°C (30.2°F) Higher cannabinoid pull, slower recovery, lower system pressure. The workhorse for shatter, budder and badder
Propane -42°C (-43.6°F) Lighter, more selective for terpenes, faster recovery, much higher system pressure. Used blended, rarely alone

Most production runs a blend. Adding propane raises the vapor pressure of the mix, which speeds recovery and lifts terpene retention, and it raises the pressure your vessels see. That is why the blend ratio is an operating decision, not a recipe detail. Pressures by temperature and blend are in REF-VP-01 Vapor Pressure.

Grade matters more than blend. Use research or analytical grade solvent. Instrument grade carries mercaptans and heavier residuals that survive into your concentrate and that no amount of purging removes. If instrument grade is all you can source, distill it several times before it touches biomass.

02. The envelope you are working inside

Limit Value
Vessel MAWP 250 psi at 200°F (93°C)
Vessel MDMT -155°F (-104°C)
Vessel hydrostatic test 325 psi at 70°F (21°C)
Chilling jacket MAWP 100 psi at 200°F (93°C)
Jacket hydrostatic test 130 psi at 70°F (21°C)
System operating range -65°C to 50°C (-85°F to 122°F)
Extraction pressure, typical 0 to 30 psi
LCO2 injection line relief 22 psi
Target vacuum before a run -29.5 inHg

Vessel figures per 3P Certz design calculation report DCR-200101-R1, 2019 ASME BPVC Section VIII Division 1. Operating range per N.B. Oler system specifications.

Extraction happens at low pressure. Typical soak and transfer pressures run 0 to 30 psi. The 250 psi MAWP is not a working pressure, it is headroom. If your process is sitting near 250 psi you have a problem, not a technique.

The operating range is narrower than the vessel rating. The vessel is designed to 200°F (93°C). The system is specified to 50°C (122°F). The lower number governs, because the limit is set by the softest component in the assembly, not by the shell.

03. What a run actually is

The number that decides your day

Recovery rate, not extraction rate, sets your cycle time. N.B. Oler runs 3/4 inch jacketed, chilled recovery lines that move 4 lb or more of solvent per minute.

  1. Chill the solvent. LCO2 or chiller fluid into the solvent tank jacket. Cold solvent means lower vapor pressure, so you can move it without fighting it.
  2. Load and chill the material columns. Cold biomass gives up less chlorophyll and less plant wax. Most of your product quality is decided here, before any solvent moves.
  3. Vacuum down to -29.5 inHg. Air is oxygen against your terpenes and a false pressure reading against your process. Hold ten minutes. Any decay is a leak, and a leak is a solvent release waiting to happen.
  4. Pressure test. Nitrogen in 10 psi steps, one step per minute, to 100 psi. Hold ten minutes. Soapy water on anything that drops.
  5. Bring the hot side up. The recovery vessel jacket drives solvent back out of solution. It cannot do that cold.
  6. Inject and soak. Soak time is a product decision. Short soaks pull terpenes and leave pigment. Long soaks pull more total mass, and more of what you will have to remediate later.
  7. Transfer. Straight to recovery, or through the de-wax vessel first if running in-line. In-line de-waxing at -30°C (-22°F) or colder adds 30 to 90 minutes and removes a separate winterization step downstream.
  8. Recover. Passive recovery through the molecular sieve back into the chilled solvent tank. No pump in the solvent path means nothing in the solvent path to rebuild.

04. Throughput, worked from real system capacity

20 LB system 40 LB system
Material columns 2 x 6" x 48" 4 x 6" x 48"
Dry material per run 9,000 g (19.8 lb) 18,000 g (39.6 lb)
Live resin per run 16,329 g (36 lb) Upgradeable to 72 lb (32.7 kg)
Run time About 1 hour About 1 hour
Rated throughput 20 lb/hr 40 lb/hr
Solvent MAQ design 100 lb (45 kg) 200 lb (91 kg)
LCO2 per run About 75 L 200 to 300 L
Heating 208V/80A or 480V/40A 24 to 48 kW at 100°F (38°C), 6 GPM

One shift on a 20 LB system

5Runs per 8 hour shift, conservative
45 kgDry biomass, about 99 lb
About 375 LLCO2 consumed

Concentrate produced depends entirely on your input material. That is deliberate. Yield is a property of your biomass, not of the machine, and two operators on identical systems will report numbers far enough apart that any single published yield figure is misleading. Run your own material, record it, and use your own number.

Where the real ceiling is. Almost nobody is limited by extraction. At five 20 LB runs a shift you are producing faster than a typical vacuum oven bank can purge and faster than a hand packaging line can keep up. Count your oven capacity and packaging labor before you buy a bigger extractor.

05. Post-processing, in one page

Output What changes
Shatter Stable, undisturbed vacuum purge. Long, low and left alone
Wax, badder, budder Agitation during or after purge. Whipping nucleates the mass
Diamonds Slow pressure decay in a sealed vessel over days to weeks, riding the saturation curve down with an adjustable relief. See Diamond Formation
Live resin Fresh frozen input, cold throughout, minimum handling. The terpene fraction is the product
Crude No selectivity applied. Feedstock for distillation or remediation

Decarboxylation, for reference

Temperature What happens
Below 100°C (212°F) Minimal, very slow
100 to 120°C (212 to 248°F) THCA conversion begins
120 to 140°C (248 to 284°F) Peak THCA to THC conversion
140 to 160°C (284 to 320°F) THC peak, highest yield
Above 160°C (320°F) THC begins to degrade

Well above the 50°C (122°F) system limit. Decarboxylation happens in dedicated equipment downstream, never in the extraction system.

06. The costs nobody quotes you

  • C1D1 booth or room build-out. Up to 12 weeks lead time, and a significant capital line of its own.
  • Bulk LCO2 storage tank. 16 or more weeks lead time. At 75 L per run on a 20 LB system, a dewar will not carry a production schedule.
  • Low temperature chiller. 20 or more weeks lead time. It needs to reach -40°C (-40°F) at minimum for standard cold extraction. For live resin, plan on -60°C (-76°F) minimum and -70°C (-94°F) recommended. It draws 480VAC / 60Hz / 3Ph / 55A or more, and should live outside because its heat load will overwhelm your HVAC.
  • Vacuum, heating and nitrogen. C1D1 rated vacuum pump at 2.8 CFM or greater, hot water recirculation at 208V/80A or 480V/40A, K-type nitrogen bottle regulated 15 to 100 psi.
  • Post-processing. Vacuum ovens, cold storage, packaging.

Order the long lead items the day you order the system, not the day it ships. The extractor arriving before the booth is finished is the most common and most expensive scheduling mistake in this industry. Current lead times: Lead Times, Published. Full utility list: Site Requirements and Utilities.

Sources. N.B. Oler system specifications; N.B. Oler Hydrocarbon Operators Manual; N.B. Oler in-house testing; 3P Certz design calculation report DCR-200101-R1. No third party industry data is used.

Questions about your system? Call the shop at 541-330-6409, Monday to Thursday, 8 to 4 Pacific, or email info@nboler.com.
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