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Table 2 Overview of important extraction methods and their efficiency for lipid recovery

From: Lipids detection and quantification in oleaginous microorganisms: an overview of the current state of the art

Method

Efficiency

Cost

Energy demands

Industrial perspective

References

Conventional solvents such as chloroform/methanol, hexane, or ether

Depends on the species of microorganism, pretreatment of biomass, moisture content, type of solvent, solvent: biomass ratio, treatment time, etc.

Mainly the cost of solvents and reactors, possible reuse of solvents, energy-intensive process

Drying of cellular biomass, heating of solvent, distillation of solvent

There are reports at a larger scale

[46]

Super critical CO2

Varies with flow rate of CO2, pressure, and exposure time

Mainly the cost of equipment and its maintenance

Distillation/heating of solvents if paired with co-solvent, maintaining high-pressure conditions

No report at an industrial scale

[47,48,49,50,51]

Liquid CO2

Requires cell disruption to achieve better yield, usually lipid yield is low

Maintenance of high-pressure conditions (15 MPa), cell disruption

Distillation/heating of solvents if paired with co-solvent

No reports at a larger scale

[52, 53]

Microwave-assisted lipid extraction

Simple, rapid process, effective for robust species, easy to scale up; does not require dewatering of microorganisms; highly efficient at lab scale

Low operating costs but high maintenance costs of equipment

High energy consumption, recovery of thermolabile compounds may require cooling

No reports at a larger scale

[10, 46, 48, 54,55,56]

Ultrasonication-assisted lipid extraction

Short extraction time, simple to operate, highly reproducible results, energy-effective in small volume, cell wall hinders lipid recovery

Mainly cost of equipment

Large volume of sample, requires high energy

Not suitable for large-scale

[46, 56,57,58,59,60,61,62,63]