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Oilseed processing and edible oil refining

Food Technology / Food Engineering (B.Tech) · Processing technologies · free study notes for exams, placements and interviews

In short

Oilseed processing converts seeds such as groundnut, mustard/rapeseed, soybean, sunflower, sesame, cottonseed, coconut and rice bran into crude oil plus a protein-rich cake, and refining then removes gums, free fatty acids, colour, odour, waxes and contaminants to give a bland, stable, food-grade oil. India is the world's largest importer of edible oil (roughly 55-60% of consumption is imported, chiefly palm, soybean and sunflower), so every step of yield and refining loss carries direct commercial weight. The topic is examined in Food Engineering, Fats and Oils Technology and Unit Operations papers, and in GATE (XE/Food Technology) through extraction, mass balance and refining-loss numericals. Employers who test it include Adani Wilmar, Cargill, Ruchi/Patanjali, Marico, Emami Agrotech, Bunge, ITC, Godrej Agrovet, Mother Dairy (Dhara) and the National Dairy Development Board's oil division, plus FSSAI and Agmark inspection roles.

Explained

Oilseeds, oil composition and quality indices

Pre-treatment and mechanical expression

  1. Cleaning: magnetic separator, sieves/destoner and aspirator remove metal, sand, chaff; dirt causes wear and darkens oil.
  2. Drying/conditioning: moisture brought to about 8-10% for decortication, later adjusted for flaking.
  3. Dehulling/decortication: groundnut, sunflower, cottonseed, soybean - removing hull raises oil content of the feed, reduces oil retention in cake and raises cake protein. Hulls are abrasive and hold oil.
  4. Size reduction: cracking rolls then flaking rolls to 0.2-0.4 mm flakes - rupturing cells shortens the diffusion path, the key to solvent extraction efficiency.
  5. Cooking/conditioning (90-110 °C, 20-30 min): coagulates protein, breaks oil cells, reduces oil viscosity, inactivates lipase and myrosinase, and adjusts moisture to about 3% - this is what makes pressing possible.
  6. Expression:
    • Ghani/kolhu (traditional): mortar-and-pestle type, low throughput, "kachi ghani" cold-pressed mustard oil sold for flavour and pungency (allyl isothiocyanate).
    • Hydraulic press (batch): cake wrapped in cloth, pressed at 100-200 bar; low capacity, residual oil 6-10%.
    • Screw press / expeller (continuous): a tapered worm in a barrel cage raises pressure along the length; residual oil 4-8% (single press) or 3-5% (double press). Pre-press is a partial press for high-oil seeds leaving 15-20% oil for extraction.
    • Cold pressing: below about 50-60 °C, retains flavour, tocopherols and colour; lower yield, higher cost - the basis of premium virgin coconut, mustard and sesame oils.
  7. Clarification: screening, settling and filter press/decanter remove press "foots"; the oil is crude oil.

Solvent extraction

Refining: chemical and physical routes

The classic sequence is degumming → neutralisation → bleaching → (winterisation/dewaxing) → deodorisation, abbreviated by the industry as refining-bleaching-deodorising (RBD oil).

  1. Degumming - removes phospholipids that would cause foaming, dark colour and settling.
    • *Water degumming:* 1-3% hot water at 60-70 °C, 30 min, hydratable gums swell and are centrifuged out → lecithin (a saleable soybean co-product).
    • *Acid degumming:* 0.05-0.2% phosphoric or citric acid removes non-hydratable (Ca/Mg salts of phosphatidic acid) gums; also chelates trace metals.
    • *Enzymatic degumming:* phospholipase A1 converts phospholipids to water-soluble lysophospholipids (phospholipase C instead splits off diacylglycerol, which stays in the oil), cutting oil loss in the gum phase.
    • Target: residual phosphorus below about 10 ppm for chemical refining, and below about 5 ppm (ideally under 3 ppm) for physical refining, which is the stricter requirement.
  2. Neutralisation (alkali refining) - caustic soda (NaOH, 10-24 °Bé) reacts with FFA to form soapstock, removed by centrifuge; followed by hot-water washing and vacuum drying. Soapstock is acidulated to acid oil for soap/oleochemicals.
    • Theoretical caustic = stoichiometric NaOH for the FFA; excess (treat) of 0.05-0.3% covers pigments and non-oil acids.
  3. Bleaching (adsorptive, not chemical whitening) - 0.2-2% activated/acid-activated bleaching earth (bentonite/Fuller's earth), sometimes with activated carbon or silica, at 90-110 °C under vacuum for 20-30 min, then filtered on a pressure leaf filter. Removes pigments, soap traces, metals, oxidation products and part of the peroxides. Spent earth retains 20-35% oil and is a fire hazard (spontaneous heating).
  4. Winterisation / dewaxing / fractionation - chilling to 5-10 °C and holding, then filtering to remove waxes (sunflower, rice bran) or high-melting glycerides; dry fractionation of palm oil gives palm stearin and liquid palm olein (the cooking oil sold in India).
  5. Deodorisation - steam stripping (sparge steam 0.5-3%) at 180-260 °C under 2-5 mbar absolute for 20-120 min in a packed or tray column; removes odour, residual FFA, aldehydes, pesticide residues and some carotenoids (heat bleaching). Tocopherols distilled off are recovered from the "deodoriser distillate" (vitamin E source; oryzanol from rice bran oil).
    • Over-heating (> about 240 °C with long hold) generates trans fatty acids and 3-MCPD esters/glycidyl esters, so modern practice uses lower temperature with longer vacuum-steam contact and good chloride control.
  6. Physical (steam) refining - degumming + bleaching followed by combined deacidification-deodorisation in one high-vacuum column; no caustic, so no soapstock and far less effluent. Best for high-FFA, low-gum oils (palm, coconut, rice bran). Chemical refining suits high-gum, low-FFA oils (soybean, mustard).
  7. Polishing/filtration, antioxidant addition and nitrogen blanketing before packing; vitamin A and D fortification (the +F logo) under the Food Safety and Standards (Fortification of Foods) Regulations, 2018.

Modification of fats and oils

Standards, regulators and by-product utilisation

Key points

Formulas and examples

Oil yield (%) = (mass of oil recovered / mass of seed processed) × 100
Extraction efficiency (%) = [(oil in feed − oil in residue) / oil in feed] × 100
Residual oil (% on meal) = (oil in meal / mass of meal) × 100
Acid value AV = (56.1 × N × V) / W — mg KOH per g oil; N = normality of KOH, V = mL titrant, W = sample mass (g)
FFA (% as oleic acid) = (28.2 × N × V) / W = AV / 1.99 (28.2 = molar mass of oleic acid 282 ÷ 10)
Peroxide value PV = (N × V × 1000) / W — meq O₂ per kg oil (N, V from Na₂S₂O₃ titration)
Saponification value SV = 56.1 × (Vblank − Vsample) × N / W — mg KOH per g oil
Iodine value IV = 12.69 × N × (Vblank − Vsample) / W — g I₂ per 100 g oil (Wijs method)
Theoretical NaOH for neutralisation = FFA(%) × (40 / 282) × mass of oil (for FFA as oleic acid; 40 = M of NaOH)
Refining loss (%) ≈ 1.5 to 3 × FFA(%) (Wesson loss factor, oil- and plant-specific)
Mean molecular mass of triglyceride ≈ 3 × 56100 / SV (g/mol)
Theoretical hydrogen for hydrogenation: 1 mol H₂ per mol of double bond saturated; ΔIV of 1 unit ≈ 0.0794 g H₂ per kg oil (2.016 / 253.8 × 10)

Example 1 - Overall mass balance on a pre-press/solvent plant. 1,000 kg of groundnut kernel with 48% oil is pre-pressed, leaving a cake with 18% oil; the cake is then extracted to 1% residual oil in the meal.

Example 2 - FFA, acid value and caustic requirement. A 5.0 g sample of crude soybean oil needs 4.5 mL of 0.1 N KOH.

Example 3 - Peroxide value and shelf-life judgement. A 10.0 g sunflower oil sample consumes 1.6 mL of 0.01 N sodium thiosulphate.

Example 4 - Hydrogenation: hydrogen demand and trans check. A soybean oil of IV 130 is hydrogenated to IV 70 to make a vanaspati base; batch size 5,000 kg.

Example 5 - Rice bran stabilisation economics. Fresh rice bran (20% oil) has 4% FFA; unstabilised bran gains 1.5% FFA per day and is extracted after 5 days.

FeatureExpeller/pressingSolvent extraction
Suited toOil content > 25%Any, essential below 25%
Residual oil in cake/meal4-8%0.5-1.5%
Capital and complexityLowHigh (solvent, safety, recovery)
Oil qualityCleaner, lower phosphatidesMore gums, colour; must be refined
Cake useEdible-grade cake, feedDeoiled cake, feed and export
HazardMechanicalHexane fire/explosion
StepRemovesTypical conditionsLoss / by-product
DegummingPhospholipids, metals60-70 °C, water or 0.05-0.2% acidGums → lecithin
NeutralisationFFA, some pigment60-90 °C, NaOH lyeSoapstock, 1.5-3 × FFA
BleachingPigments, soap, peroxides90-110 °C, vacuum, 0.2-2% earthSpent earth (20-35% oil)
WinterisationWaxes, hard glycerides5-10 °C, hold, filterWax/stearin
DeodorisationOdorants, residual FFA180-260 °C, 2-5 mbar, steamDeodoriser distillate (tocopherols)

Where it is used

Interview questions

Common mistakes

Related topics

Fats and oils chemistry: rancidity and antioxidants · Unit operations: leaching, distillation and evaporation · Frying and bakery fats · Food analysis and quality control of fats · Food safety law: FSSAI standards and labelling · Food plant safety and effluent treatment

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