Supercritical carbon dioxide
Supercritical carbon dioxide (scCO₂) is the supercritical fluid state of carbon dioxide maintained at or above its critical temperature of 31.1 °C (304.1 K) and critical pressure of 73.8 bar (7.38 MPa), where the distinction between liquid and gas phases vanishes, yielding a homogeneous phase with hybrid physical properties.[1][2][3] In this regime, scCO₂ demonstrates gas-like diffusivity and low viscosity alongside liquid-like density, enabling tunable solvency that varies with pressure and temperature, which facilitates precise control in chemical processes without leaving toxic residues upon depressurization to gaseous CO₂.[4][5] These attributes render scCO₂ a non-flammable, low-toxicity alternative to conventional organic solvents, widely adopted in industrial applications such as caffeine extraction from coffee beans, essential oil recovery from plants, precision cleaning in electronics manufacturing, and as a working fluid in advanced power generation cycles for enhanced thermodynamic efficiency.[6][7][8] Emerging uses extend to enhanced oil recovery, pharmaceutical particle engineering, and sterilization processes, capitalizing on its ability to penetrate materials and dissolve compounds selectively under mild conditions.[9][10]Definition and Fundamental Properties
Critical Point and Phase Transition
The critical point of carbon dioxide marks the end of the liquid-vapor coexistence curve in its phase diagram, where the distinction between the liquid and gaseous phases vanishes, resulting in a supercritical fluid state above this threshold. For CO₂, this occurs at a critical temperature of 304.13 K (31.0 °C) and a critical pressure of 7.377 MPa (73.8 bar).[11] At this point, the fluid's density is approximately 468 kg/m³, and properties such as viscosity and diffusivity become continuously tunable without phase separation.[12] Crossing the critical point via isothermal compression or isobaric heating eliminates the meniscus between liquid and vapor phases, transitioning CO₂ into a supercritical state characterized by intermediate properties: gas-like low viscosity and high diffusivity combined with liquid-like density and solvency. This phase transition is particularly accessible for CO₂ compared to other substances like water, whose critical point requires 374 °C and 22.1 MPa, enabling practical laboratory and industrial manipulation near ambient temperatures.[13] Near the critical point, the fluid exhibits high compressibility, where minor changes in temperature or pressure induce significant density fluctuations, enhancing its responsiveness as a tunable medium.[1] In the supercritical regime, CO₂'s phase behavior defies classical liquid-gas categorization, as density gradients persist without a sharp interface, allowing for phenomena like piston-like expansions observed in high-pressure cells. This unique transition underpins applications requiring adjustable solvent strength, as the fluid's solvating power correlates directly with its density, which spans from gas-like (low pressure) to liquid-like (high pressure) values above the critical locus.[14] Empirical measurements confirm that at pressures just above critical, thermal perturbations cause rapid density shifts, underscoring the causal role of intermolecular forces weakening at the critical isochore.[15]Physical Properties and Tunability
Supercritical carbon dioxide (scCO₂) forms when carbon dioxide exceeds its critical temperature of 31.1 °C (304.13 K) and critical pressure of 73.8 bar (7.38 MPa), eliminating the meniscus between liquid and vapor phases and yielding a homogeneous fluid with hybrid properties.[1] In this regime, scCO₂ demonstrates liquid-like densities ranging from approximately 0.3 to 1.0 g/cm³, gas-like low viscosities on the order of 10⁻⁵ to 10⁻⁴ Pa·s, and diffusivities intermediate between gases (∼10⁻⁵ cm²/s) and liquids (∼10⁻⁶ cm²/s), facilitating enhanced mass transfer compared to traditional solvents.[16][2] These thermophysical attributes arise from the absence of phase boundaries, allowing molecular clustering without full liquefaction.[17] The tunability of scCO₂ stems from its sensitivity to variations in temperature and pressure, which directly modulate key properties like density, dielectric constant, and solvating power.[1] For example, at fixed temperature above the critical point, elevating pressure from near-critical levels to hundreds of bar can increase density by factors of 2–3, shifting solvency from nonpolar gas-like behavior to more liquid-like extraction capability.[18] Near the critical pressure, compressibility peaks, amplifying property changes with minor perturbations; density may fluctuate dramatically over small temperature shifts, as quantified in equations of state like Span-Wagner, which model deviations from ideal gas behavior with high fidelity.[1][19] This adjustability—without phase changes—enables precise control, such as lowering viscosity for better flow in reactors or boosting diffusivity for rapid solute penetration.[20]| Property | Typical Range in scCO₂ | Comparison to Phases |
|---|---|---|
| Density (g/cm³) | 0.2–1.1 | Liquid: ∼0.9–1.0; Gas: ∼0.001–0.002 |
| Viscosity (Pa·s) | 2×10⁻⁵ – 10⁻⁴ | Liquid: ∼10⁻³; Gas: ∼10⁻⁵ |
| Diffusivity (cm²/s) | 10⁻⁵ – 10⁻⁴ | Liquid: ∼10⁻⁶; Gas: ∼10⁻¹ |
Chemical Behavior and Solubility Characteristics
Supercritical carbon dioxide (scCO₂) demonstrates chemical inertness under typical operating conditions, exhibiting low reactivity except in the presence of strong bases or water, where it can form carbonic acid (H₂CO₃) with a pH of approximately 2.85.[22] Its non-polar nature, characterized by a low dielectric constant ranging from 1.1 to 1.5, renders it suitable as a solvent for non-polar and low-molecular-weight compounds while limiting interactions with polar or ionic species.[22] Additionally, scCO₂ possesses gas-like diffusivity and low viscosity alongside liquid-like densities (0.1–1.0 g/cm³), facilitating penetration into solid matrices without the mass-transfer limitations of conventional liquids.[22][23] Solubility in scCO₂ is primarily governed by the fluid's density and the solute's polarity, with high solubility observed for non-polar hydrocarbons and weakly polar organics, but poor performance for polar substrates unless modified by co-solvents such as ethanol or surfactants like perfluorinated compounds.[23][24] For instance, fluorinated polymers with molecular weights below 15,000 g/mol exhibit enhanced solubility, while ionic or high-molecular-weight species require additives to form stable microemulsions or reverse micelles.[24] The solvent's solvating power is lower than that of traditional organic solvents, enabling selective extraction based on molecular clustering rather than broad dissolution.[23] Solubility characteristics are highly tunable through adjustments in pressure and temperature, which directly modulate scCO₂ density and thus solvent strength; solubility generally increases with pressure at constant temperature due to rising density, as exemplified by solubility enhancements from 252 g/L to 257 g/L for certain hydrocarbons when pressure rises from 100 to 200 bar at 40°C.[25][24] Temperature effects are more variable, often showing an initial increase followed by a decrease at constant pressure owing to competing influences on vapor pressure and density, with a characteristic crossover point determined empirically via models like Chrastil's equation: C = \rho^k \exp(a/T + b), where C is solute concentration, \rho is density, T is temperature, and a, b, k are solute-specific constants.[25] Near the critical point (31.1°C, 72.8 bar), small perturbations in these parameters yield dramatic changes in solubility, enabling precise control in processes like extraction.[24] Upon depressurization below the critical pressure, solubility plummets, facilitating solute precipitation and solvent recovery without additional separation steps.[25][23]Historical Development
Early Scientific Observations
Thomas Andrews identified the critical point of carbon dioxide in 1869 during investigations into gas liquefaction. Through precise pressure-volume-temperature measurements, he determined that CO₂ transitions to a supercritical state above 31.1°C and 73.8 bar, where the distinction between liquid and gas phases vanishes, preventing liquefaction by pressure alone regardless of magnitude.[26][27] This observation established the foundational concept of critical parameters, revealing that intermolecular forces limit compressibility beyond this threshold.[28] In 1879, J.B. Hannay and J. Hogarth extended these findings by examining solubility of solids in compressed gases, including supercritical CO₂. They reported that substances like iodine and calcium chloride dissolved markedly in fluids above the critical point, with solubility increasing with density, and precipitated as fine particles—"like snow"—upon depressurization.[29][30] These experiments demonstrated the solvent-like behavior of supercritical fluids, tunable via pressure and temperature, though initial interpretations focused on gas-phase dissolution rather than recognizing the phase's hybrid properties.[31] Early 19th-century experiments with CO₂ under high pressure had hinted at anomalous behaviors, such as reduced compressibility near phase boundaries, but lacked systematic analysis until Andrews' work.[32] These observations laid empirical groundwork for understanding supercritical states, emphasizing density-driven properties over traditional phase categorizations.Industrial Pioneering and Key Milestones
The pioneering of supercritical carbon dioxide (scCO₂) for industrial applications began with extraction processes in the food sector, driven by the need for solvent-free alternatives to chemical methods. In 1967, German chemist Kurt Zosel at the Max Planck Institute observed the selective solubility of caffeine in scCO₂, leading to a patented process for coffee decaffeination by 1970.[33] This marked the foundational shift from laboratory curiosity to viable technology, leveraging scCO₂'s tunable density to dissolve and separate compounds without residues or thermal degradation.[34] The first commercial implementation occurred in Germany during the early 1970s, with scCO₂ decaffeination plants established for green coffee beans, processing them under pressures around 200-300 bar and temperatures near 40-60°C to achieve over 97% caffeine removal while preserving flavor volatiles.[34] By the late 1970s, this expanded to tea and pharmaceuticals, demonstrating scCO₂'s scalability for thermally sensitive materials and prompting investments in high-pressure equipment.[35] These early plants, such as those operated by Studiengesellschaft Kaffee-Chemie, validated the process's economic feasibility, with extraction yields comparable to organic solvents but without solvent recovery costs.[28] A key milestone in diversification came in 1978, when researchers developed scCO₂ extraction for hops, enabling isomerized alpha acid isolation for brewing under subcritical to supercritical conditions (up to 3000 psi and 110°F), which by 1982 saw commercial operation by SKW/Trostberg for producing pure hop extracts free of pesticides and waxes.[36] This application highlighted scCO₂'s precision in fractionating lipophilic compounds, influencing the global hops industry by reducing solvent use and improving product purity.[37] Parallel advancements in the 1970s introduced scCO₂ to enhanced oil recovery (EOR), where the fossil fuel sector deployed it to mobilize crude from reservoir rocks via miscible flooding, achieving displacement efficiencies up to 20-30% higher than waterflooding in pilot tests.[27] By the 1980s, firms like Phasex pioneered botanical extractions beyond food, including essential oils and pharmaceuticals, solidifying scCO₂ as a cornerstone for green chemistry processes.[38] These milestones underscored the technology's transition from niche solvent to industrial standard, predicated on empirical demonstrations of selectivity and recyclability.Core Applications
Solvent Extraction Processes
Supercritical carbon dioxide (sCO₂) extraction exploits the fluid's liquid-like density and gas-like diffusivity to selectively dissolve non-polar to moderately polar solutes from solid matrices, enabling efficient separation without residual solvents. Operating above the critical point (31.1°C, 7.38 MPa), the process involves pumping CO₂ into an extractor vessel containing the feedstock, where it solubilizes target compounds; the laden fluid then flows to a separator, where depressurization precipitates the extract while gaseous CO₂ is recompressed and recycled in a closed loop, achieving recovery rates exceeding 95%.[34] This closed-cycle design minimizes environmental impact and operational costs compared to organic solvent methods, with extraction efficiency tunable via pressure (typically 10-40 MPa) and temperature (35-80°C) to target specific molecular weights and polarities.[39] A primary industrial application is coffee decaffeination, where sCO₂ selectively removes 97-99.9% of caffeine from green beans while retaining aroma volatiles and antioxidants. The process, commercialized in Germany in 1980 by Maximus Coffee Group, preconditions beans by water immersion to enhance caffeine diffusivity, then employs sCO₂ at 15-30 MPa and 50-80°C for 4-10 hours per batch, followed by caffeine adsorption onto activated carbon for CO₂ regeneration.[40] This method preserves bean integrity better than methylene chloride or ethyl acetate alternatives, yielding decaffeinated coffee with flavor profiles closer to regular beans, as evidenced by sensory panel tests showing reduced bitterness loss.[41] In essential oil production, sCO₂ extracts heat-sensitive terpenes, sesquiterpenes, and flavonoids from botanicals like lavender, hops, and citrus peels, producing solvent-free oils suitable for food, cosmetics, and pharmaceuticals. For lavender (Lavandula angustifolia), optimal conditions of 10-20 MPa and 40-50°C yield 4-6% oil by mass, rich in linalool and linalyl acetate, surpassing steam distillation in selectivity and avoiding hydrolysis of esters.[42] Hop extraction for brewing isolates alpha acids (humulones) at 12-15 MPa and 50°C, delivering isomerized bittering agents with 30-50% higher purity than solvent methods, reducing beer oxidation risks.[43] Co-solvents like 5-10% ethanol enhance polar compound recovery in hybrid processes, as demonstrated in citrus peel extractions achieving 2-4% naringin alongside oils.[44] Beyond food, sCO₂ facilitates pharmaceutical extractions, such as polyisoprenoids from plant tissues or cannabinoids from hemp, under 20-30 MPa to isolate bioactive fractions with minimal degradation.[45] Industrial scalability is supported by techno-economic analyses showing internal rates of return up to 40% for biomass processing plants, with payback periods of 2-3 years, driven by low CO₂ costs (under $0.50/kg) and energy inputs of 5-10 kWh/kg extract.[46] Limitations include poor solubility of highly polar compounds without modifiers and high capital costs for pressure vessels, though these are offset by regulatory approvals for "natural" labeling in the EU and FDA.[34]Energy Systems and Working Fluid Uses
Supercritical carbon dioxide (sCO₂) serves as a working fluid in advanced power cycles, particularly the Brayton cycle, where it operates above its critical point of 31.1 °C and 7.38 MPa, enabling high-density fluid behavior akin to a liquid while retaining gas-like expansion properties.[47] This configuration allows for reduced compression work compared to traditional steam or air cycles, as the fluid's incompressibility near the critical point minimizes energy input during the compression stage, potentially achieving thermal efficiencies exceeding 45% with access to low-temperature heat sinks.[48] The U.S. Department of Energy has identified sCO₂ cycles as promising for higher efficiency and lower capital costs in electricity generation, with applications spanning temperatures from 450 °C to over 700 °C.[49] In the recompression Brayton cycle, a common sCO₂ configuration, the working fluid undergoes compression in two stages, with partial heating and recuperation to maximize efficiency; this setup has demonstrated potential efficiencies above 50% through optimizations like shunting or intercooling.[50] The cycle's compactness arises from sCO₂'s high turbine inlet densities—up to 100 times that of steam—allowing smaller turbomachinery footprints, which reduces material costs and enables modular deployment.[51] For concentrated solar power (CSP), sCO₂ integrates with particle receivers or molten salts, as tested at Sandia National Laboratories' Solar Thermal Test Facility in 2020, where particle-to-sCO₂ heat exchangers achieved initial heat transfer demonstrations at scales up to 1 MWth.[52] Nuclear applications leverage sCO₂ for advanced reactors, including fluoride-salt-cooled high-temperature reactors, where the cycle supports decay heat removal and power conversion with efficiencies 5-10% higher than steam Rankine cycles at equivalent temperatures.[53] The Supercritical Transformational Electric Power (STEP) program, initiated by the DOE in the 2010s, has advanced sCO₂ turbomachinery for nuclear and fossil systems, culminating in a 10 MWe pilot plant demonstration by the Gas Technology Institute targeting operational validation by 2021.[54] In fossil fuel contexts, sCO₂ enables oxy-fuel combustion integration, as pursued by NETL's R&D program since 2010, with a turbine technology pilot successfully demonstrated in December 2024, confirming scalability for supercritical pressures up to 30 MPa.[55] [56] Geothermal and waste heat recovery systems also employ sCO₂ for closed-loop operations, as in a 2020 California Energy Commission demonstration circulating sCO₂ in subsurface loops to simulate power generation from low-grade heat sources below 200 °C.[57] Combined cycle optimizations, analyzed in 2025 studies, show exergy efficiencies improved by 10-15% over baseline systems when sCO₂ operates at 800 °C and 25-30 MPa, though real-world deployment remains limited by challenges in high-temperature recuperator durability.[58] These uses underscore sCO₂'s role in enhancing overall plant efficiency by 5-8% relative to steam cycles in mid-temperature ranges (500-700 °C), driven by favorable thermodynamic properties rather than reliance on exotic materials.[59]Enhanced Oil Recovery and Geological Applications
Supercritical carbon dioxide (scCO2) is injected into oil reservoirs for enhanced oil recovery (EOR) primarily via miscible flooding, where it achieves miscibility with crude oil above the minimum miscibility pressure of approximately 1200 psi, thereby reducing interfacial tension to near zero, swelling the oil volume by up to 30-50%, and decreasing its viscosity by factors of 10 or more to mobilize residual oil toward production wells.[60] These effects stem from scCO2's liquid-like density and gas-like diffusivity at reservoir conditions (typically >1073 psi and >31.1°C), enabling efficient extraction of hydrocarbons, particularly lighter crudes (27-48° API gravity).[60] [61] In water-alternating-gas (WAG) variants, alternating slugs of water and scCO2 (ratios 0.5-4.0, slug sizes 0.1-2% pore volume) improve volumetric sweep efficiency by mitigating CO2 channeling in high-permeability zones, yielding incremental recoveries of 4-15% of original oil in place (OOIP) beyond primary and secondary methods, with pilots reaching up to 22%.[60] The first commercial scCO2 EOR project commenced in 1972 at the SACROC Unit in the Permian Basin, Texas, marking the onset of widespread adoption; by 2008, U.S. CO2 EOR produced 240,000 barrels per day, consuming over 11 trillion cubic feet (560 million metric tons) of CO2, predominantly sourced from natural reservoirs.[60] Notable case studies include the Wasson Field's Denver Unit, Texas, which recovered over 120 million incremental barrels by 2008 (current incremental production ~26,850 barrels/day), and the Weyburn Field, Canada, achieving 130 million incremental barrels while sequestering 585 billion cubic feet (30 million metric tons) of CO2 via 95 million cubic feet/day injection.[60] In tight shale reservoirs, scCO2 huff-and-puff cycles exploit molecular extraction and diffusion, enhancing recovery by 4-5% over non-supercritical CO2 under reservoir conditions, though challenges like early breakthrough limit field-scale efficiency without additives.[62] [8] In geological applications, scCO2 facilitates permanent sequestration in deep sedimentary formations such as depleted hydrocarbon reservoirs, saline aquifers, and coal seams, where it is injected at depths exceeding 800 meters to remain supercritical, leveraging structural trapping under low-permeability caprocks (e.g., shales) as the primary retention mechanism, supplemented by solubility in brines (up to 50-100 kg/m³), residual saturation via capillary forces, and mineral trapping through reactions forming carbonates over millennia.[63] U.S. storage capacity estimates range from 2,600 to 22,000 Gt CO2, with global potential at 2,000 Gt; operational sites like Sleipner, Norway (1 Mt/year since 1996), demonstrate injectivity requiring formation permeabilities >10-100 mD for Mt-scale rates, though risks include induced seismicity (e.g., <M1 events at In Salah) and leakage via faults if caprock integrity fails.[63] Beyond storage, scCO2 enables hydraulic fracturing in low-permeability geological formations like shale and basalt, where its near-zero surface tension and low viscosity (0.02-0.08 cP) generate complex fracture networks at pressures 20-50% lower than water-based fluids, increasing permeability by 10-100 times post-treatment via proppant-free propagation and geochemical alteration, as observed in lab tests on shale samples exposed to 8-12 MPa scCO2. [64] This application suits water-scarce regions for stimulating tight reservoirs or enhanced geothermal systems, though permeability reductions of 26-52% can occur from adsorption and swelling in fractures saturated with scCO2.[65] EOR-integrated sequestration, as in Weyburn, couples recovery with net CO2 retention (e.g., 0.2-0.3 barrels oil per ton stored), but long-term monitoring is essential to verify trapping efficacy against buoyancy-driven migration.[60]Materials Processing and Manufacturing
Supercritical carbon dioxide (scCO₂) is employed as a non-toxic, recyclable solvent in polymer processing, facilitating impregnation of additives into polymers, blending of immiscible polymers, and formation of polymer composites without relying on volatile organic compounds.[66] This approach leverages the tunable solvating power of scCO₂, achieved by varying pressure and temperature above its critical point (31.1°C, 7.38 MPa), to penetrate polymer matrices and deposit functional materials upon depressurization.[67] Applications include enhancing mechanical properties or adding antimicrobials to thermoplastics, with processing conditions typically at 10-40 MPa and 40-100°C to ensure compatibility with heat-sensitive polymers.[68] In microcellular foaming, scCO₂ functions as a physical blowing agent, saturating molten or solid polymers under high pressure to dissolve up to 10-20 wt% CO₂, followed by controlled depressurization to nucleate gas bubbles and form foams with uniform cell sizes of 10-100 μm and densities as low as 0.05 g/cm³.[69] This batch or continuous extrusion process, often at 10-25 MPa and 100-200°C, produces lightweight foams from materials like polypropylene or polyurethane, offering advantages over chemical blowing agents by avoiding residue and enabling precise control over expansion ratios up to 50-fold.[70] Industrial adoption includes automotive parts and insulation, where scCO₂ foaming yields structures with improved energy absorption compared to conventional methods.[71] Particle formation via rapid expansion of supercritical solutions (RESS) utilizes scCO₂ to dissolve solutes such as pharmaceuticals or polymers, followed by supersonic expansion through a nozzle at rates exceeding 100 m/s, precipitating nanoparticles with sizes typically 10-500 nm and narrow size distributions (polydispersity <0.2).[72] This solvent-free technique, operating at 10-40 MPa and 40-80°C, avoids milling or grinding, reducing contamination and enabling scalable production for drug delivery or pigments, though particle agglomeration can occur without stabilizers.[73] Variants like RESS-SC (with solid cosolvents) enhance yields for poorly soluble compounds, achieving up to 90% precipitation efficiency.[74] In semiconductor manufacturing, scCO₂ enables precision cleaning and drying of wafers by removing photoresists, residues, and watermarks through surfactant-assisted dissolution and evaporation, operating at 10-30 MPa and 40-60°C to minimize defects below 1% compared to aqueous rinses.[75] This dry process integrates with lithography steps, stripping ion-implanted resists without silicon etching, as demonstrated in 200 nm node fabrication where supercritical conditions reduced chemical usage by over 90%.[76] Additional uses include low-k dielectric deposition and silylation, supporting feature sizes down to 45 nm by exploiting CO₂'s low surface tension (<1 mN/m).[75]Advantages, Limitations, and Criticisms
Empirical Benefits and Efficiency Gains
Supercritical carbon dioxide (sCO₂) power cycles demonstrate notable efficiency improvements over traditional steam Rankine cycles, particularly in high-temperature applications such as concentrated solar power and nuclear reactors. Empirical analyses indicate that replacing steam cycles with sCO₂ Brayton cycles can yield net plant efficiency gains of 6.2% to 7.4% in coal-fired plants, attributed to the fluid's favorable thermodynamic properties including high density and low compressibility, which enable compact turbomachinery and reduced compression work.[77] In recompression configurations, cycle efficiencies have reached up to 51.82%, surpassing comparable Rankine cycles by enabling higher turbine inlet temperatures and better heat recovery through recuperators.[78] These gains stem from sCO₂'s ability to maintain supercritical states across a wide temperature range (above 31.1°C and 7.38 MPa), minimizing exergy losses during heat addition and rejection.[79] In solvent extraction processes, sCO₂ enhances yield and selectivity for bioactive compounds from biomass, often outperforming conventional organic solvents by leveraging its tunable density and diffusivity. Studies on natural product extraction report yield improvements of up to 20-30% for thermolabile antioxidants and essential oils, due to the fluid's gas-like penetration and liquid-like solvency, which facilitate rapid mass transfer without thermal degradation.[26] For instance, in fruit seed oil recovery, sCO₂ extraction achieves higher purity extracts at lower temperatures (typically 40-60°C), reducing energy input by avoiding distillation steps required for solvent removal in hexane-based methods.[80] The process's recyclability—CO₂ is depressurized and reused—further boosts operational efficiency, with overall energy consumption reported 10-20% lower than subcritical alternatives in scaled industrial setups.[34] For enhanced oil recovery (EOR), sCO₂ injection in tight reservoirs and carbonates has empirically increased recovery factors by 4-10% over gaseous CO₂ flooding, primarily through reduced interfacial tension and improved sweep efficiency via the fluid's miscibility with hydrocarbons under reservoir conditions (e.g., 100-200°C, 10-30 MPa).[62] Core-flood experiments in heterogeneous carbonates show ultimate oil recovery rates up to 60-70% of original oil in place with sCO₂ huff-and-puff cycles, compared to 50-60% for waterflooding, as the supercritical phase extracts asphaltene fractions and expands oil volume for better displacement.[81] In materials processing, such as particle micronization and polymer foaming, sCO₂ enables rapid depressurization processes that achieve uniform microstructures with 15-25% higher throughput than melt-based methods, minimizing energy use through solvent-free operation and avoiding post-processing residues.[82]| Application | Key Efficiency Metric | Improvement Over Baseline | Source |
|---|---|---|---|
| Power Cycles | Net Plant Efficiency | +6.2-7.4% vs. Steam Rankine | [77] |
| Extraction | Yield for Bioactives | +20-30% vs. Organic Solvents | [26] |
| EOR | Recovery Factor | +4-10% vs. Gaseous CO₂ | [62] |
| Materials Processing | Throughput | +15-25% vs. Melt Methods | [82] |