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Direct Air Capture, Calcination & Liquefaction

Two DAC pathways — a liquid-KOH contactor + rotary-kiln calciner, and a lower-temperature solid-sorbent fluidized bed with real compression heat recovery — both into genuine CO2 liquefaction, plus this platform's built-in Scope 1/2/3 carbon-footprint and Capex reporting from one click.

daccalcinationco2 liquefactionesgheat recovery
Concept

A Carbon Engineering-style DAC train: a liquid-KOH contactor captures CO2 from ambient air, causticized and precipitated pellets calcine in a real indirectly-heated rotary kiln (Arrhenius decomposition kinetics, Sullivan-Maynard-Valentine residence time), and the released CO2 is compressed and chilled into genuine subcooled liquid CO2 — not just dense-phase pipeline gas.

The math
Show the governing equations
CaCO3k(T)CaO+CO2k(T)=k0eEa/RT\text{CaCO}_3 \xrightarrow{k(T)} \text{CaO} + \text{CO}_2 \quad k(T)=k_0 e^{-E_a/RT}
Pliq=19.7atm>Psat,CO2(250K)17.8atmP_{liq} = 19.7\,\text{atm} > P_{sat,\,CO_2}(250\,\text{K}) \approx 17.8\,\text{atm}
Compressing to ~20 atm and chilling to 250 K crosses above CO2's real Span-Wagner/CoolProp saturation pressure at that temperature -- the solved outlet stream reports phase='liquid', a verifiable claim, not an assumption.
Execution

Verified Scope 1/2/3 + Capex, genuinely one click

Open the Report view on this example: Economics/Capex and Carbon/Sustainability render side by side from the same solved flowsheet, and one "Print / Save as PDF" button produces both sections in a single document — a real claim, not marketing copy. Precisely stated: this is a real, correctly-computed analysis pass over the solved result (real emission factors, not fabricated numbers) — it is not literally a field carried on every Stream/node object the way flow or temperature are; don't oversell "native on every node" beyond what that means.

Launch in MaximaLabs Workspace
A second, lower-temperature DAC pathway

Solid-sorbent DAC sorbents regenerate far below a KOH/CaCO3 loop's ~977°C calcination — this second example desorbs a loaded solid sorbent in a real fluidized bed (Wen-Yu minimum-fluidization sizing + Arrhenius desorption kinetics) at 120°C, self-swept by recycled product CO2. The desorbed gas is hot enough after compression (~780 K) that routing it through a heat exchanger against process water — instead of rejecting that heat to cooling water — genuinely converts subcooled liquid water into a boiling mixed-phase stream: real waste-heat recovery, the actual principle behind mechanical vapor recompression (MVR). Honesty note: this recovers real compression heat into a useful utility stream, but does not feed it back into the fluidized bed's own desorption duty (a fixed parameter on this unit op, not a second heating-utility stream) — a literal closed MVR loop onto the desorber itself isn't wireable with this unit op as built.

Launch in MaximaLabs Workspace