GB1580181A

GB1580181A - Fat separation process

Info

Publication number: GB1580181A
Application number: GB651/76A
Authority: GB
Original assignee: Unilever PLC
Current assignee: Unilever PLC
Priority date: 1976-01-08
Filing date: 1976-01-08
Publication date: 1980-11-26
Also published as: JPS604868B2; FI63055C; IE44210B1; NL7700106A; IE44210L; FI63055B; FR2337759A1; NO148557B; BE850088A; FR2337759B1; DE2700302A1; ZA7762B; LU76532A1; AU2102377A; DK144735C; DK144735B; SE7700134L; MY8400098A; NO770012L; FI770002A

Description

(54) FAT SEPARATION PROCESS (71) We, UNILEVER LIMITED, a company organised under the laws of Great Britain, of Unilever House, Blackfriars, London E.C.4, England, do hereby declare the invention for which we pray that a patent may be granted to us and the method by which it is to be performed, to be particularly described in and by the following statement:- This invention relates to separating solid particulate matter from fatty material, particularly fatty acids and their esters, especially fats. More particularly the invention relates to fractionation processes applied to such substances.

The separation of solid particulate matter from liquid fatty material in which it is dispersed is effected in the course of refining and fractionation operations. In the latter, selected fatty acids or glycerides in fats or glyceride oils may be precipitated as solid particles, usually by cooling and separated for example by filtration from others remaining in liquid phase, sometimes dissolved in solvents.

In these operations, the separation of the solid and liquid phases is often slow; the precipitate on the form of particles may retain a high proportion of the liquid component of the fatty material by adsorption and drainage of liquid phase components from it may be poor, even with centrifugation, especially in recrystallisation operations. Repeatedly washing the solid matter to remove the liquid clinging to it may be necessary but takes up more time and is extravagant of solvent.

Although, therefore, more complete separation may be highly desirable, whether to improve the quality of the solid phase of the yield of the liquid, it is in any case time-consuming and expensive and may even be impractical.

In the process of the present invention the particulate matter is converted to an aggregate form more readily separated from the liquid phase by draining, the process comprising subjecting fatty material in liquid form containing the particulate matter dispersed therein, to homogeneous agitation as hereinafter defined until aggregation of the particles takes place, and separating the liquid fatty material therefrom.

Homogeneous agitation is defined as agitation providing a velocity gradient which is the same between any two particles in the mixture adjacent radially to one another. Under the influence of the homogeneous agitation particles coalesce into agglomerates which are much more easily drained of adherent liquid phase in the subsequent separation operations.

Ideal conditions of homogeneous agitation are possibly only for ideal Newtonian liquids in lam-inar flow. In practice some departure from these ideal conditions is to be expected where solid particles are present and Taylor conditions of turbulence are promoted with the accompanying formation of vortices in the system.

Homogeneous agitation is preferably effected by a stirrer with a smooth profile. Turbulence in the fatty material undergoing homogeneous agitation should be minimised. Homogeneous agitation, giving streamline flow is provided by a stirrer with a smooth and regular profile, as by a cylindrical stirrer concentric with and rotating in a chamber containing the fatty material, on a vertical, inclined or horizontal axis.

The radial dimensions of the stirrer are not critical, but small stirrers may be slower to affect aggregation, other things being equal. Preferably the diameter of the stirrer is from one-third to two-thirds the diameter of the agitation chamber, particularly about half its diameter, but it preferably extends substantially the full depth of the fatty material in the chamber, to ensure complete stirring. The depth is itself not critical in relation to the radial dimensions, at least in batch operations, but it is at any rate preferably at least as great as the radial width of the annulus of fatty material enclosed between the walls of the chamber and the stirrer, more particularly twice as deep or more. A particular feature of the invention is that no auxiliary fluid is required to promote aggregation of the particles.

The speed of the stirrer should preferably be as slow as is consistent with achieving the desired effect, preferably from 1 to 200, especially 10 to 100 r.pm., preferably corresponding to a velocity gradient of from 1 to 250 m/min/m, especially 10 to 100 m/min/m. radially. Where the observed aggregation is unduly slow to develop with a small stirrer, it is best to replace it with a bigger stirrer operated at the same or slower speeds, to obtain quicker aggregation.

The process is suitable for batchwise or continuous operation but in the latter event preferably the chamber is deep relative to the annulus width to provide several mixing stages in the annular zone containing the fatty material and combine good mixing with maximum contact between the liquid and solid material.

The invention is of particular importance for fractional crystallisation of fatty acids and their esters, especially fats. These include glyceride oils which are normally liquid. Fractional crystallisation may be applied to remove impurities or to separate particular fractions of the fatty material having desired melting characteristics and may be carried out in the presence or absence of solvent for the fatty material, although the process is particularly valuable in so-called dry fractionation processes in the absence of a solvent, when substantially longer filtration times are incurred due to the high viscosity of the liquid oleine fraction.

This may be separated by washing the crystals with an aqueous dispersion of a suitable surfactant as in the so-called Lanza process. Suitable solvents for fat fractionation include acetone, hexane or nitropropane and methanol for fatty acids, preferably containing a little water. The amount of solvent may vary from 5:1 to 1:2 by weight relative to the fatty material. Other solvents known in the art may also be used.

Preferably the fractional crystallisation is effected in situ during homogeneous agitation, the fatty material being cooled from a wholly liquid or dissolved condition until crystallisation of the fraction to bE separated is complete, at the same time subjecting the material to homogeneous agitation. Apparatus for the purpose preferably comprises a stirring chamber fitted with a coaxial stirrer, both of smooth cylindrical shape and size as described, and cooling means for cooling for contents of the chamber, preferably through the walls of the chamber and of the stirrer. A lower limit may be necessary to the speed of rotation of the stirrer, in order to ensure adequate heat transfer and avoid excessive deposition of crystal growth on the cooling surfaces, which hampers heat transfer.In contrast to many forms of crystallisation apparatus, the stirrer should not scrape the walls of the cooling chamber. Such means do not provide homogeneous agitation.

The cooling rate is also affected by the temperature differential between the cooling surface and the fatty material. Large temperature differentials promote rapid cooling but with the formation of micro-crystalline growth. Small temperature differentials, on the other hand, produce larger crystals but much more slowly.

Temperature differentials specified in this specification are measured to the centre of the liquid and are preferably below 10"C measured radially. A temperature differential of from 5 to 20 centigrade degrees, preferably 5 to 10 centrigrade degrees, is preferably maintained between the coolant and the body of the liquid undergoing cooling, at least until crystals appear. Thereafter a higher differential can be provided, but preferably not exceeding 25 centigrade degrees, especially 10 to 20 centigrade degrees.

The invention may be applied to both edible and non-edible vegetable, animal and marine fats, their fractions and hydrogenated and interesterified derivatives and their constituent fatty acids, for example tallow, palm, sunflower, safflower, groundnut, soyabean and lauric oils.

The invention is useful for carrying out winterisation. This is a form of fractional crystallisation commonly applied to edible oils, for example palm or cottonseed oil, or soyabean oil which is slightly hydrogenated to improve its resistance to deterioration in storage, which are intended for use as salad oils or frying oils, to prevent the onset of turbidity on standing at ambient temperatures, due to the fractional crystallisation of a higher-melting stearine fraction in the oil.

In winterisation processes the stearine is removed by filtration after cooling the oil but substantial losses can be incurred in conventional winterisation processes for the reasons above stated, in the separation of the oleine and stearine fractions and in any case a small amount of the stearine often stubbornly remains in the oil, to crystallise out later in storage, unless the oil is cooled to much lower temperatures, with the loss of even more oil. The present invention provides an economic and efficient winterisation process, incurring minimum oil losses and providing maximum effectiveness.

The invention is also effective for fractionating fatty material for the recovery of a substantial proportion of higher-melting solid fraction in a single fractionation, as much as a quarter of the total weight of the fatty material. In conventional practice the solid fraction commonly absorbs at least twice its own weight of the lower melting, liquid fraction. Solid fractions of above about a quarter of the total weight treated therefore form slurries, the separation of which into their constituent liquid and solid fractions is extremely difficult, whether by filtration of centrifugation. In accordance with the present invention the crystals are aggregated together and retain a substantially lower portion of the liquid fraction.

The process of the invention may be carried out at temperatures for example from -20 C to 500 C, temperatures being limited only by the physical limits of solvents, where these are used, and the amount of solids to be removed, not more than 35 and at least 5% being preferred. Separation of the agglomerated solid matter may be, for example, by decantation or by gravitation or pressure filtration or by centrifugation.

The invention is of particular importance for the recovery of fat fractions having desired attributes for use in the food industry. In the formulation of margarine fats for example blends are often prepared of fats obtained by fractionation procedures to meet desired physical or chemical characteristics. The fats may for example be required to meet specified melting characteristics, or a high poly-unsaturated fatty acid content may be required for dietary purposes.

Careful fractionation in accordance with the invention enables fats to be obtained to meet such requirements. In the confectionary industry also hard butters are obtainable with the critical melting performance required of fats used for this purpose by fractionation in accordance with the invention, particularly from palm oil but also from other vegetable fats which may be hardened before or after fractionation.

EXAMPLE 1 A cylindrical crystalliser chamber fitted with a dished base and a cover plate was also provided with a cylindrical rotor, fixed to a vertical rotor shaft extending into the chamber, which was rotatable by motor means mounted above the plate and was supported in bearings located in the centre of the cover plate and the dished base of the chamber.

The chamber was approximately half as deep again as it was wide and the rotor, extending substantially the full depth of the chamber, half as wide as the chamber, The chamber itself was fitted with an external cooling jacket in which aqueous ethylene glycol solution, cooled to a predetermined temperature, could be circulated.

Soyabean oil was lightly hydrogenated to an Iodine Value of 110 to 112 using a fresh, supported nickel catalyst. This improves the stability of the oil against oxidative deterioration but leads to cloudiness in the oil on standing, due to the crystallisation of a stearine fraction. This was removed from the oil in accordance with the invention using the apparatus described.

After removing the catalyst the oil was cooled to 360C and charged to the crystalliser chamber. The agitator was rotated to give a velocity gradient of about 15 metres/minute/metre (n the liquid in the annulus. Aqueous ethylene glycol circulated in the cooling jacket was maintained to provide a temperature gradient of 200metre measured radially through the oil, to a measuring point midway between the walls of the vessel and the rotor. When the temperature reached 21"C crystals appeared and the temperature differential increased to 350C/metre until a final temperature of 3"C was reached. The oil was then filtered through a standard vacuum filtration unit, yielding 74% of an oleine in 3 hours, by weight of the hydrogenated oil.The oleine remained clear at OOC for at least 5 hours. On the other hand the hydrogenated whole oil deposited stearine crystals even on standing at 20"C.

In a comparative trial using conventional fractionation methods incorporating an agitator in the vessel instead of the rotor stirrer and scraping attachments for removing crystalline material forming on the walls of the vessel, conditions were adjusted to give a similar filtration time, but a yield of only 60 /n was obtained. The oleine product in both instances was suitable for use as a frying oil, remaining clear in storage at ambient conditions.

EXAMPLE 2 A series of experiments was carried out by fractionating similar hardened soyabean oil, charged at 300C in similar equipment, comprising a chamber 60 cm diameter and 1 metre high, fitted with a rotor stirrer 30 cm diameter. The effect was observed on filtration speed and oleine yield of fractionation temperature and temperature differential which, however, remained constant in each experiment, in all of which the rotational speed was 42 r.p.m. corresponding to a velocity gradient of 264 m/hour/m. The effect was also observed of "stabilisation" by maintaining the cooled fat for 2 hours at the fractionation temperature.

From all the experiments an oleine was obtained which remained clear at 0 C after 5 hours. Further particulars appear in the Table below.

TABLE Cooling Conditions

Stabili- Time Yield Filtration Diffl. sation Final (hours) Oleine rate experiment "C time (hours) "C from 30"C /n M3/m2/h.

10 67.6 5.2 la 2 # 12 65.7 4.0 O 2 10 0 | 6 63.6 0.99 10 2a # 2 # 8 60.8 0.68 3 6 -1.5 7 61.3 0.63 Experiments 1 and 2 demonstrate the marked decrease in filtration speed and considerable increase in oleine yield that follows when At is reduced, for the same final temperature.Comparison of Experiments 1 and la and again 2 and 2a surprisingly shows that a "stabilisation" period at the fractionation temperature is deleterious, contrary to conventional fractionation practice. Finally, Experiment 3 also shows that a good oleine yield can be obtained, comparable with Experiment 2a, even at the lower temperature of -1.5"C, by maintaining a lower At and avoiding a prolonged stabilisation temperature.

EXAMPLE 3 Palm oil (I.V. 53) was stirred at 100 r.p.m. in a cylindrical vessel twice as deep as wide, fitted with a cooling jacket and a coaxial cylindrical rotor extending substantially the full depth of the oil, the diameter of the rotor being half that of the vessel. From 50"C the oil was cooled at 120C per hour to 280C, at which temperature it was maintained with continued stirring for 5+ hours, when NMR analysis of a sample showed 8% solids, formed. The oil was filtered at the same temperature, with a flow rate of above 10 m3/m2 per hour at a filtration pressure of 0.5 atmospheres.

The filtrate was 80 /n of original palm oil, leaving a residue of 20% retained by the filter.

The Example was repeated in continuously operating equipment of the same proportions, using a stirrer speed of 40 r.p.m., 9% solids being reported and the filtrate again amounting to 80 /n of the original oil, with an Iodine Value of 57 and a filtration rate of 6.5 m3/m2 per hour. Residence time was 2 hours.

At a crystallisation temperature of 13"C and a stirrer speed of 80 r.p.m., a yield of 45% liquid fraction was recovered from the continuous equipment, with an I.V.

of 63.2 to filtration rate of 0.5 m3/m2 per hour. This is an excellent recovery considering the heavy residue to be removed. Residence time was 5 hours.

EXAMPLE 4 Malayan palm oil fraction (I.V. 58.4), obtained by dry fractionation of palm oil, was mixed with four times its weight of acetone and fractionated at 30C by cooling in the batch apparatus described in Example 3, from 50"C to 30C at the rate of 12"C per hour with stirring at 300 r.p.m. After stirring for 3 hours at this temperature filtration was rapid and the filtration residue was washed four times, each time with 1+ times the weight of starting oil, of acetone. After evaporating off solvent a residue of 36% (I.V. 41.3) was obtained with a filtrate oil yield of 64% (I.V.

68.5), based on the starting oil.

EXAMPLE 5 Example 4 was repeated at -6"C, cooling from 30"C with 5 hours' stabilisation, using as solvent an equal amount by weight of hexane. After washing the filtration residue twice, each time using an equal amount by weight of the starting oil of hexane, and evaporating off the solvent, a filtrate oil of 64.1 by weight of the starting oil was recovered of I.V. 67.8 and a residue of 35.90/, of I.V.

43.2.

EXAMPLE 6 Tallow fatty acids of I.V. 56 were dissolved in 1+ times their weight of a mixture of 92 /n methanol with 8% water and fractionated in the apparatus described in Example 3, by cooling from 30"C to -70C at a cooling rate of 18"C per hour with stirring at 200 r.p.m. and immediately thereafter filtered off as before and washed twice with the same solvent, each time with 88% of the original weight of acid.

After evaporating of the solvent a filtrate of I.V. 95.2 in 56.10/, yield was recovered together with 43.9 filtration residue I.V. 5.8, obtained as a free-flowing granular material 920/, of the particles of which had a diameter about 0.5 mm.

WHAT WE CLAIM IS: 1. Process for separating solid particulate matter from liquid fatty material in which it is dispersed, the process comprising subjecting the fatty material in liquid form containing the particulate matter, to conditions of homogeneous agitation as hereinbefore defined until aggregation of the particles takes place and separating the liquid fatty material from the aggregated particles.

2. Process according to Claim 1 in which homogeneous agitation is provided in a chamber containing the fatty material by a cylindrical stirrer concentric therewith.

3. Process according to Claim 2 in which the chamber is cylindrical and its diameter is one-and-a-half to three times the diameter of the stirrer.

4. Process according to Claim 2 or 3 in which the chamber is at least as deep as the radial width of the annulus of fatty material enclosed in the chamber between the walls thereof and the stirrer.

5. Process according to any of the preceding claims in which the stirrer is rotated at a speed providing a velocity gradient from 1 to 250 m/minute/m radially.

6. Process according to Claim 5 in which the velocity gradient is from 10 to 100 m/minute/m radially.

7. Process according to any of the preceding claims in which the stirrer is rotated at a speed from 10 to 100 r.p.m.

8. Process according to any of the preceding claims in which the particles comprise components of the fatty material which are selectively precipitated while the fatty material is subjected to homogeneous agitation.

9. Process according to Claim 8 comprising cooling the fatty material to effect precipitation.

10. Process according to any of the preceding claims in which a temperature differential below 10 C measured radially is applied to cool the fatty material.

11. Process according to Claim 9 or 10 in which the fatty material is maintained at constant temperature after cooling to stabilise the precipitate.

12. Process according to any of the preceding Claims 8 to 11 in which from 5 to 35 /n of the fatty material is precipitated.

13. Process according to any of the preceding claims in which the fatty material comprises fat.

14. Process according to Claim 13 in which the fat comprises palm oil or a fraction thereof.

15. Process according to Claim 13 in which the fat comprises soyabean oil.

16. Process according to any of the preceding claims in which a solvent for the fatty material is present.

17. Process according to any of the preceding claims in which the solvent comprises hexane, acetone or nitropropane.

18. Process according to Claim 16 in which the amount of solvent present is from 5:1 to 1:2 parts by weight of the fatty material.

**WARNING** end of DESC field may overlap start of CLMS **.

Claims

**WARNING** start of CLMS field may overlap end of DESC **. temperature filtration was rapid and the filtration residue was washed four times, each time with 1+ times the weight of starting oil, of acetone. After evaporating off solvent a residue of 36% (I.V. 41.3) was obtained with a filtrate oil yield of 64% (I.V. 68.5), based on the starting oil. EXAMPLE 5 Example 4 was repeated at -6"C, cooling from 30"C with 5 hours' stabilisation, using as solvent an equal amount by weight of hexane. After washing the filtration residue twice, each time using an equal amount by weight of the starting oil of hexane, and evaporating off the solvent, a filtrate oil of 64.1 by weight of the starting oil was recovered of I.V. 67.8 and a residue of 35.90/, of I.V. 43.2. EXAMPLE 6 Tallow fatty acids of I.V. 56 were dissolved in 1+ times their weight of a mixture of 92 /n methanol with 8% water and fractionated in the apparatus described in Example 3, by cooling from 30"C to -70C at a cooling rate of 18"C per hour with stirring at 200 r.p.m. and immediately thereafter filtered off as before and washed twice with the same solvent, each time with 88% of the original weight of acid. After evaporating of the solvent a filtrate of I.V. 95.2 in 56.10/, yield was recovered together with 43.9 filtration residue I.V. 5.8, obtained as a free-flowing granular material 920/, of the particles of which had a diameter about 0.5 mm. WHAT WE CLAIM IS:

1. Process for separating solid particulate matter from liquid fatty material in which it is dispersed, the process comprising subjecting the fatty material in liquid form containing the particulate matter, to conditions of homogeneous agitation as hereinbefore defined until aggregation of the particles takes place and separating the liquid fatty material from the aggregated particles.

15. Process according to Claim 13 in which the fat comprises soyabean oil.

19. Process for the preparation of fractionated fatty material substantially as

described with reference to the accompanying Examples.

20. Fats and fatty acids whenever fractionated by a process substantially as hereinbefore described.