NZ750901B2 - Method for purification of animal or vegetable fats - Google Patents

Abstract

Present invention relates to a novel process for purification of lipid material for further use as such as e.g. a source of fuel or chemicals.

Description

Title: Method for purification of animal or vegetable fats TECHNICAL FIELD Present invention relates to methods for purification of lipid materials, especially lipid als originating from biological material. The method enables removal of impurities from the lipid material. In particular, the invention relates to methods for purifying lipid materials conventionally seen as containing levels of impurities too high to be commercially profitable to use in a purification process to obtain a purified feedstock of a quality allowing the use thereof as a source of fuel or chemicals. The impurities may be of a character that conventional methods are not able to remove from the feedstock to such a degree that is prescribed as the appropriate quality for further use as a source of fuel or chemicals.

BACKGROUND ART US 3758533 relates to a method for removing polyethylene ties from tallow and like fatty materials. In the , the fatty material is heated to a temperature to about 95 °C or below but above the melting temperature of the fatty material to render the polymeric ties ble in the fatty material and separating the ties. The separation of ties can be conducted by filtration or centrifuging. According to the teachings of US 3758533 separation of hylene impurities by settling is not possible since the density of polyethylene is only a little greater than that of tallow (866 kg/m3).

US 7262311 relates to a method for removing phospholipids and other impurities from crude vegetable oil using physical refining ques. In the method, the crude oil is allowed to settle over a period of time, such as 20 days, such that the oil tes into a gums layer and oil layer which are separated from each other. The purified oil contains from 25 ppm to 110 ppm of phosphorus.

US 2601375 relates to a method for ring of vegetable oils from sludge or settlings, which accumulate in vegetable oil storage tanks. In the method, the sludge is mixed and heated with water and the mixture is allowed to cool and settle into an upper oil phase and lower aqueous phase with solid impurities. The ted lower phase can be treated with alkali followed by acid treatment.

SUMMARY OF THE INVENTION Present invention provides for an efficient method of purification of lipid material. The lipid material is specifically originating from biological origin.

Consequently, present invention relates to a method for purifying lipid al, characterized in that the method comprises the following steps; a) storing the lipid material in a ng tank at elevated temperature, b) allowing the impurities to settle to the bottom of the settling tank to thereby form an oily sludge phase, c) separating the formed oily sludge phase from the rest of the lipid material, d) further processing the lipid material e) optionally purifying said separated oily sludge phase from impurities, and optionally f) returning the purified oil from the purifying step e) to said settling tank.

In present ion the term "lipid material" should be understood as meaning any al having a biological origin. Specifically the term may thus denote tall oil pitch or the residual bottom on from tall oil distillation processes, animal based oils or fats, fish based oils or fats, vegetable based oils or fats such as e.g. sludge palm oil and used cooking oil or oil used in deep frying, microbial or algae oils. Other examples are e.g. plant oils, plant fats, animal fats and animal oils, and mold oils. Specifically, the term may comprise ed oil, canola oil, colza oil, tall oil, sunflower oil, soybean oil, hemp oil, olive oil, linseed oil, cottonseed oil, mustard oil, palm oil, arachis oil, castor oil, coconut oil, animal fats such as suet, tallow, blubber, ed alimentary fats, starting materials produced by genetic engineering, and biological starting materials produced by es such as algae and bacteria. It is to be understood that the term may comprise a mixture of any of the above ned examples.

The lipid material used in the process may also be fossil based, such as e.g. various oils used and produced by the oil industry. Non-limiting examples are various petroleum products such as e.g. fuel oils and gasoline (petrol). The term also encompasses all used products in either the refining process or e.g. used lubrication oils, waste plastic, sis oils and the likes.

The impurities present in the lipid material may be of various character or origin.

Specifically, the impurities are such that they may be harmful in the process or they may render the al useless for its ultimate intended use. The impurities may be of metallic or polymeric origin such as tary metals or for example phosphorous compounds. Specifically, the polymeric impurities that are removed may be e.g. commonly used plastics such a polyethylene (PE).

Notably, it has surprisingly found that the method as described herein is effective with respect to the time used to te the purification process. Consequently, present invention es for a cation method allowing a shorter time to purify the lipid material.

BRIEF DESCRIPTION OF THE DRAWINGS Figure 1 illustrates the set-up of the AF settling test and the settling drum. Fig. 1a illustrates the side view (left hand) of the drum as well as the top-view (right hand). Fig. 1b illustrates a detailed side view of the settling drum and the various location wherein the samples and fractions are collected.

Figure 2 rates the various amounts of impurities present in the s taken from the purification process ing to the invention in relation to purification time. Fig. 2a illustrates the amount of polyethylene (PE), Fig. 2b illustrates the amount of solid material, Fig. 2c illustrates the amount of phosphor (P), Fig. 2d illustrates the amount of calcium (Ca), and Fig. 2e illustrates the amount of nitrogen (N).

Figure 3 rates the ing flux of animal fat at week 0 ("nolla") and week 5 ("vko "), samples taken from the middle of the settling vessel.

Figure 4 illustrates the bleaching flux of sludge (acid degummed), sludge (heat treated and filtered) and original AF832 feed.

W0 2018/060324 Figure 5 illustrates the flow scheme of the acid degumming and bleaching process. tions The following abbreviations will be used in the speciation PG atidyl glycerols PE Phosphatidyl lamines Pl Phosphatidyl ols PC Phosphatidyl cholines PA Phosphatidic acids LPA Lysophosphatidic acids LPC Lysophosphatidyl cholines SM Sphingomyeline PHO Phospholidids PGLY Phosphatidyl glycerols AF Animal fat DETAILED DESCRIPTION Present invention relates to a method for purifying a lipid material. In one aspect the invention relates to a method comprising the steps of: a) storing the lipid material in a settling tank at elevated temperature, b) allowing the impurities to settle to the bottom of the settling tank to thereby form an oily sludge phase, c) separating the formed oily sludge phase from the rest of the lipid material, d) further processing the lipid material e) optionally purifying said ted oily sludge phase from impurities, and optionally f) returning the purified oil from the purifying step e) to said settling tank.

Specifically, the invention relates to a method for purifying lipid material, c h a r a c t e r i z e d in that the method comprises the following steps; a) storing the lipid material in a settling tank at elevated temperature, b) allowing the impurities to settle to the bottom of the settling tank to thereby form an oily sludge phase, c) separating the formed oily sludge phase from the rest of the lipid material, d) further processing the lipid material e) ing said separated oily sludge phase from impurities, and optionally f) returning the purified oil from the purifying step e) to said settling tank, wherein the method is c h a r a c t e r i z e d in that step e) comprises a heat treatment step comprising the steps of; i. heating said oily sludge phase to a temperature of from about 150oC to about 300oC, ii. adding polar solvent to said oily sludge phase for removal of impurities from oil phase such as e.g. phosphorus or calcium compounds, and iii. separating and ring ed oil.

In a particular aspect, the t invention provides a method for purifying lipid material, wherein the method comprises the following steps; a) storing the lipid material in a settling tank at elevated temperature, b) allowing the impurities to settle to the bottom of the settling tank to thereby form an oily sludge phase, c) separating the formed oily sludge phase from the rest of the lipid material, d) further processing the lipid material e) purifying said ted oily sludge phase from ties, and ally f) ing the purified oil from the purifying step e) to said settling tank, wherein step e) comprises a heat treatment step comprising the steps of; [FOLLOWED BY PAGE 5a] i. heating said oily sludge phase to a temperature of from about 150oC to about 300oC, ii. adding polar solvent to said oily sludge phase for removal of impurities from oil phase such as e.g. orus or calcium nds, and iii. separating and recovering purified oil and, wherein said elevated temperature in step a) is from about 40°C to about 120°C.

The lipid material to be used in present invention is a lipid material to be purified into a material that may serve as a source for fuel of any kind. The important factor is that the purified lipid material has to be of such a quality that it can serve as a fuel or be used in further processes such as e.g. catalytic cracking without containing levels of impurities that may e.g. jeopardize the full functionality of an engine or poisoning of catalysts or otherwise hampering of any further processes that the ed lipid material may be subjected to. Such further processes may be e.g. catalytic ng, thermo-catalytic cracking, catalytic reatment, fluid catalytic cracking, catalytic ketonization, catalytic esterification, or catalytic dehydration. The purified lipid material may also be further processed into various chemicals, such as bulk chemicals (e.g. polymers, solvents, solvent components and lubricants) or specialty als (e.g. cosmetics and pharmaceuticals).

[FOLLOWED BY PAGE 6] WO 60324 2017/074611 In the art, there are various methods for purification of lipid material for the purposes mentioned herein. However, lipid material that contains high level of impurities may not be able or le to be purified by techniques known in the art such that the purified lipid material contains low levels of impurities allowing it to be used as a source of fuel.

Present invention solves this problem by the method as disclosed herein, thereby allowing use of a lipid material that would normally be seen as uneconomical or unsuitable for cation.

Lipid material according to the invention may be, but is not limited to, any lipids containing phosphorous and/or metals and/or polymers such as e.g. s plastics.

Examples of lipid materials are tall oil pitch or the al bottom fraction from tall oil distillation processes, animal based oils or fats, vegetable based oils or fats such as e.g. sludge palm oil and used cooking oil or oil used in deep frying, microbial or algae oils, free fatty acids, used or spent lubrication oils or other types of waxes. Other examples of lipid material are plant oils, plant fats, animal fats and animal oils, algae, yeast and mould oils. It is to be understood that lipid material may be a mixture of any of the above mentioned examples of lipid materials. Suitable biological raw als include rapeseed oil, canola oil, colza oil, tall oil, sunflower oil, soybean oil, hemp oil, olive oil, linseed oil, seed oil, mustard oil, palm oil, arachis oil, castor oil, coconut oil, animal fats such as suet, , blubber, recycled alimentary fats, starting materials produced by genetic engineering, and biological starting materials produced by microbes such as algae and bacteria.

Exemplified lipid material include, but is not limited to: 0 Tall oil pitch (TOP), residual bottom on from tall oil distillation process, 0 Low quality animal fat (AF), not accepted for product y (very high N, PE, metals, phosphorus contents etc.), o Sludge palm oil (SPO) with very high iron t. SPOs are waste oils collected from water ponds located near palm oil mills, . Used cooking oil (UCO), may contain high level of oligomers and chlorides The lipid material used in the process may also be fossil based, such as e.g. various oils used and produced by the oil industry. Non-limiting examples are various petroleum products such as e.g. fuel oils and gasoline (petrol). The term also encompasses all used products in either the refining process or e.g. used lubrication oils, waste plastic, pyrolysis oils and the likes.

These lipid materials need to be purified in order to lower the level of elements known to render the material useless for its ultimate intended use.

The impurities present in the lipid material may originate from the lipid material itself or the impurities may originate elsewhere, e.g. from the earlier sing of the lipid material. The present ion may be used for l of any impurity that can be separated from the lipid material by settling.

The lipid material to be purified may contain impurities containing metals and phosphorus in the form of phospholipids, soaps or salts. Moreover, the lipid material may contain polymers and specifically polymers in the context of plastics. Notably such cs may be e.g. polyethylene (PE). r, any plastic polymer may be removed according to the ion. ary plastics may Bakelite, polystyrene, polyvinyl chloride, poly(methyl methacrylate), rubber or synthetic , polyester, polyethylene terephthalate, polyvinylidene chloride, polypropylene, high impact polystyrene, polyamides, acrylonitrile butadiene styrene, polyethylene/acrylonitrile butadiene styrene, polycarbonate, rbonate/acrylonitrile butadiene styrene, polyurethanes. It is also to be understood that the term polymer may comprise a blend of different plastics and/or rubbers.

Metal impurities that may be present in the lipid material may be e.g. alkali metals or alkali earth metals, such as sodium or potassium salts or magnesium or calcium salts or any nds of said metals. The ties may also be in form of phosphates or sulphates, iron salts or organic salts, soaps or e.g. phospholipids. ional techniques to remove impurities from lipids or fats consist of degumming and bleaching. ln degumming impurities are removed by addition of acid and water and the separation of impurities is performed by gravitational separation by e.g. centrifugation. However, as noted in prior art, settling as part of a purification method is not considered feasible since this requires a large amount of time, typically in the range of several weeks such as e.g. more than 5 weeks.

Present invention has the benefit of using a simple method comprising ng of the lipid material. Moreover, in the method according to the invention the lipid material may be purified as such without addition of any other al during the heat treatment.

Thus t method provides for a simplified yet effective procedure which reduces the need for addition of other constituents or chemicals which may ionally be needed when purifying similar material. Notably, the purification method can be completed within days.

The present invention provides improvements to the purification of lipid material by reducing the loss of material during purification and by improving the purity of the lipid material in the tank. The purified and separated oily sludge of the present invention may be returned to the setting tank y improving the overall purity of the lipid material in the tank. If the oily sludge is not purified and remains in the tank as such, the impurities remain in the settling tank increasing the total amount of impurities in the tank.

According to the ion, the process of purification takes place under heating.

Specifically, according to the invention, the elevated temperature and settling in step a) and b) is such that the temperature is sufficiently high to allow the lipid material to be purified to become liquid. Thus the lipid material is to about 40°C to about 120°C, such as e.g. about 50°C to about 110°C, such as e.g. about 60°C, about 100°C, or about 40°C, about 50°C, about 60°C, about 70°C, about 80°C, about 90°C, about 100°C, about 110°C or about 120°C.

The time during which the lipid material is heated and held at the desired temperature is about 5 hours to about 14 days, such as e.g. about 2 days to about 10 days, such as e.g. about 3 days to about 7 days, or about 10 hours, about 15 hours, about 1 day, about 2 days, about 3 days, about 4 days, about 5 days, about 6 days, or about 7 days.

Ideally the time during which the desired temperature is held is about 5 hours, about hours, about 15 hours, about 1 day, about 2 days, about 3 days, about 4 days, about 5 days.

It should be noted that the ng process may be executed without any ion or stirring. However, a slow agitation or stirring which does not hinder the ng may be executed. 2017/074611 After completion of the settling step b), the lipid al is separated from the formed oily sludge. This process may comprise ation of the lipid material from the oily sludge which may form a separate phase with the lipid material.

The lipid material is then further sed in any process depending on the intended use of the lipid material. The lipid material may be further processed as such or after r purifications. Such processes are e.g. hydrotreatment or co-processing. The separated oily sludge may be further purified from any impurities. Thus, the further purification of the oily sludge may comprise any suitable method such as hydrolysis or e.g. filtration, centrifugation and/or other mechanical removal of particulate impurities from the oily sludge. This purification step as outlined in step d) of present invention may comprise heating as part of the purification step.

Overall, the purification of the oily sludge may entail a process comprising the steps of i. g said oily sludge phase, ii. adding solvent to said oily sludge phase for removal of impurities from oil phase such as e.g. phosphorus or calcium compounds, and iii. separating and recovering purified oil.

The g in step i) may be in the interval of from about 100°C to about 350°C, such as e.g. about 150°C to about 300°C, or about 170°C to about 240°C, or about 200°C to about 250°C, or about 180°C to about 200°C. Preferably, the heating is in the interval of about 180°C to about 200°C.

The solvent used in step ii) may be a polar or non-polar solvent. For example, polar solvent may be water or any other suitable polar solvent such as e.g. an alcohol such as e.g. methanol, iso-propanol or any ation thereof. Moreover, the polar solvent may be a combination of water with a suitable alcohol or mix of alcohols.

The purified oil may be further subjected to a filtration step as needed in order to remove any solid residues such as e.g. metal impurities formed in step ii). However any suitable separation method may be employed such as e.g. centrifugation and/or mechanical removal. It is also to be understood that a combination of the mentioned techniques for removal of impurities may be employed.

The purified and separated oil may also be subjected to a bleaching step.

Optionally, the ed and separated recovered oil, may be recycled back to the settling tank in step a) of the invention.

The impurities that may be removed by the method of the invention are as mentioned . Notably, the impurities are one or more of polyethylene, calcium salts, sodium or phosphorous salts of any kind.

With respect to polyethylene, the method of the invention s at least about 90 %, such as e.g. at least about 95%, such as e.g. at least about 97%, such as e.g. at least about 98 %, such as e.g. at least about 99 % of the original content of polyethylene in the lipid material. Consequently, the lipid material purified by the method of present invention has a polyethylene content of below about 50 ppm, such as e.g. below about ppm, such as e.g. below about 20 ppm, such as e.g. below about 15 ppm, such as e.g. below about 10 ppm, such as e.g. below about 5 ppm. The same holds true for any of the herein mentioned plastics.

Thus the method ing to the invention provides for a purified lipid material that is suitable for further use such as e.g. a source of fuel or als, such as bulk chemicals or specialty als.

In one aspect, the invention relates to the following items: 1. A method for purifying lipid material, characterized in that the method comprises the ing steps; a) storing the lipid material in a settling tank at elevated temperature, b) allowing the impurities to settle to the bottom of the settling tank to thereby form an oily sludge phase, c) separating the formed oily sludge phase from the rest of the lipid material, d) further sing the lipid material e) optionally purifying said separated oily sludge phase from impurities, and optionally f) returning the purified oil from the ing step d) to said settling tank.

. The method according to item 1, characterized in the said elevated temperature in step a) is from about 40°C to about 120°C.

. The method according to any of the preceding items, wherein settling in the settling tank takes place without any form of stirring.

. The method according to any of the preceding items, wherein the time during which the impurities in the lipid material is allowed to settle to the bottom of the settling tank is from e.g. about 5 hours, about 10 hours, about 15 hours, about 1 day, about 2 days, about 3 days, about 4 days, about 5 days.

. The method according to any of the preceding items, wherein the lipid material is originating from biological material.

. The method according to item 5, n the lipid material is selected from e.g. used cooking oil, ble oils or any kind or animal fats of any kind or mixtures thereof.

. The method according to any of the preceding items, n the lipid material is selected from any fossil based oil or product, such as e.g. various oils used and ed by the oil industry, such as e.g. fuel oils and gasoline l), ing all used products in either the refining process, or e.g. used lubrication oils, waste plastic pyrolysis oils and the likes.

. The method according to item 1 or 2, characterized in that said separation step in step c) comprises phase separation such as e.g. by decantation, whereby the lipid material is separated from the oily sludge.

. The method according to item 1 or 2, characterized in that said purifying step d) comprises filtration, centrifugation and/or other mechanical removal of particulate impurities from the oily sludge.

.The method according to any of the previous items, characterized in that said purifying step d) comprises a heat treatment step. 11.The method according to item 10, characterized in that said heat treatment step in step d) comprises the steps of i. heating said oily sludge phase to a temperature of from about 150°C to about 300°C, ii. adding polar solvent to said oily sludge phase for removal of impurities from oil phase such as e.g. phosphorus or calcium compounds, and iii. separating and recovering purified oil. 12.The method according to item 11, wherein the g in step i) is performed during a period of about 5 to about 60 s, such as e.g. about 10 minutes to about 50 minutes, such as e.g. about 15 minutes to about 40 minutes, such as e.g. about 20 minutes to about 30 minutes. 13.The method according to item 11 or 12 wherein the g in step , i) is about 170 °C to about 240°C, preferably about 180°C to about 200°C. 14.The method ing to item 11, 12 or 13, wherein the polar solvent is water, methanol or ethanol or any combination thereof.

.The method according to item 11, wherein the recovered purified oil in step ii) is subjected to a tion and/or centrifugation and/or mechanical removal to remove impurities present in the sludge. 16.The method according to any of the preceding items, wherein the separated and recovered purified oil is further ted to a bleaching step. 17.The method according to any of the ing items, wherein impurities are one or more of polyethylene, calcium salts, sodium salts or phosphorous salts. 18.The method according to any of the preceding items wherein at least about 90 %, such as e.g. at least about 95%, such as e.g. at least about 97%, such as e.g. at least about 98 %, such as e.g. at least about 99 % of the original content of polyethylene in the lipid material is removed. 19.A purified lipid al obtainable by the method according to any of items 1- , characterized in that the purified lipid material has a polyethylene content of below about 50 ppm, such as e.g. below about 30 ppm, such as e.g. below about 20 ppm, such as e.g. below about 15 ppm, such as e.g. below about 10 ppm, such as e.g. below about 5 ppm. 20. Use of a purified lipid material obtainable by the method according to any of the preceding items, as a source of fuel or chemicals, such as e.g. bulk chemicals or specialty chemicals.

EXAMPLES Example 1 Settling test procedure The target of the settling test was to get understanding and follow settling of polyethylene and other impurities in the liquid animal fat (AF).

The test set up ed 200 l drum with homogenized animal fat. The drum was equipped with 6 sampling points, 2 in the upper part (1), 2 in the middle part (2) and 2 in the bottom (3). Samples were taken from each level from the middle (S) and from the side (U) of the drum (cf. Figure 1).

The AF was settled about 5 weeks at 60 °C without ng. Samples were taken weekly and e.g. PE, P, N, metals, PE, solid al and particle counting were analyzed. 4 ons were obtained while emptying the drum: - F1 Main product fat from the taps - F2 Remaining fat fat recovered with hand pump (after fat level went below lowest tap) - F3 Sludge mixture of fat/solid al poured from the drum - F4 Sediment solid material scraped from the bottom of the drum The results showed excellent removal of PE and good removal of solid material, Ca and Si. Fair good removal of P and Mg was also ed (table 1).

Table 1. Reduction of the impurities in animal fat after 5 weeks settling.

Solid materialm Example 2 Settling test 2 The test set up included a 200 l acid ant drum with about 140 kg homogenized animal fat. Before the test animal fat was melted and homogenized at 60 °C. Samples (1000 ml) were taken from seven sampling points: two in the upper part (1), two in the middle part (2) and two in the bottom (3). Samples from each of these levels were taken from the middle (S) and from the side (U) of the drum. One sample was taken from the bottom of the drum. The animal fat was settled at 60 °C in heating chamber without stirring for about 1 week. The samples were taken at zero point, after 5 h and after 1, 2, 3, 6 and 8 days.

WO 60324 2017/074611 P, N, metals, PE, H20 and solid material were analyzed from the samples. 1000 ml s were taken from each sampling point. On day 8 the oil level dropped below S1 and U1 taps and sample U1 was only recovered. (cf. Fig. 1b) 3 fractions were obtained while emptying the drum: F1 42 kg fat from below sampling tap 2 F2 47 kg fat recovered from sampling tap 3 F3 50 kg fat recovered from the bottom ng tap (P) F4 No sediment obtained Results of settling test 2 The results after settling for 8 days were compared to the average results of 0 days.

The bottom samples were not taken into account. Excellent removal of PE, good removal of solid material, Ca, Si and Fe and fairly good removal of P and Mg was observed (Table 2).

Table 2 Reduction (%) N -1 PE 93 P 23 Al 0 Fe 38 Na -4 Si 41 Ca 45 Mg 28 Mn 0 Solid material 63 Excellent removal of PE (93 wt-%), good removal of solid material (63 wt-%) and metals like Ca (45 wt-%), Si and Fe, fairly good removal of P (23 wt-%) and Mg was observed. PE concentration was higher on the surface part of the drum than inside the drum. PE, as well as solid material, P and metals are concentrated to the bottom right after 2nd day, dramatically on 3rd day and reduces after that. Nearly all PE was removed on day 8. See figures 2a-2e for the respective results in a graphical representation.

Example 3 Settling test no 3 Target was to settle animal fat (AF) with continuous ff from bottom valve. The test was med in about 200 l acid resistant feed tank with two sampling , one in the bottom and one from the center of the tank. The tank was equipped with circulating heating cable and other outer parts were sealed. 6 x 30 l canisters of animal fat were melted in heating chamber at 60 °C and removed to the feed tank by transfer (feed) pump. The fat was then homogenized by recycling it from the bottom to the top with transfer pump for 1,5 h and with bubbling nitrogen from the bottom. After this the fat settled for 6 days t stirring at 60 °C. Used settling temperature was measured from the side and from the inside of the vessel. The melted fat was continuously drained from the bottom valve and the prominent pump was used to keep the flow constant (~0,8 ml/min) during the settling. Sampling times were: zero point, after 5 h, 1, 2, 3 and 6 days.

P, N, metals, PE and solid material were analyzed. Results present the average of each sampling time. Additionally olipids and H20 from the simulation samples.

Table 3 Analysis s from samples taken from the center of the vessel Opoint, 0-5 h, 5-24 h, 24-48 h, 48-72 h, 72-144 h, bottom bottom bottom bottom bottom bottom Time Min 0 300 1157 1445 1525 Flow g/min 0 0,91 0,62 0,74 0,75 Sample g 1826 272,1 720,9 1071 1140 ISO PE mg/kg 141 109 781 2155 712 90 6656 Nofalab ISO PE wt-ppm nd nd nd nd 949 861 6656 Neste oil ASTMD N mg/kg 470 470 500 550 490 460 4629 ENISO H20 mg/kg 850 nd nd nd nd 390 12937 lSO663 Solid wt-% 0,09 0,1 0,42 0,67 0,26 0,08 material ASTMD Al mg/kg <0,3 <0,3 <0,3 <0,3 0,3 0,3 5185 ASTMD Fe mg/kg 1,3 1,7 3,4 8,5 3,2 1,3 5185 ASTMD Na mg/kg 60 58,1 64 60,2 60,8 54,8 5185 ASTMD Si mg/kg 0,9 6,4 3,7 5,5 2,7 0,9 5185 ASTMD Ca mg/kg 40,2 40,1 116 297 109 36,7 5185 ASTMD Mg mg/kg 4,3 4,3 9,4 19 8,2 4 5185 ASTMD P mg/kg 65,9 64,9 104 239 114 64,3 5185 ASTMD Mn mg/kg <0,3 <0,3 <0,3 0,4 <0,3 <0,3 5185 Table 4 Analysis results from samples taken from the centre of the . 0 point, 0-5 h, 5-24 h, 24-48 h, 48-72 h, 72-144 bottom bottom bottom bottom bottom h, bottom Time Min 0 300 1157 1445 1525 Flow g/min 0 0,91 0,62 0,74 0,75 Sample 9 1872 1818 1172 1728 1735 ISO PE mg/kg 132 121 101 6 <1 3 6656 Nofalab ISO PE wt-ppm 176 nd nd nd nd 16 6656 Neste oil ASTMD N mg/kg 470 460 470 470 460 460 4629 ENISO H2O mg/kg 880 nd nd nd nd 380 12937 ISO663 Solid wt-% 0,12 0,1 0,11 0,08 0,07 0,06 material ASTMD Al mg/kg <0,3 <0,3 <0,3 <0,3 0,3 0,3 5185 ASTMD Fe mg/kg 1,3 1,3 1,3 1,1 1 1 5185 ASTMD Na mg/kg 56,7 57,3 57,3 53,4 52,9 53,7 5185 ASTMD Si mg/kg 0,9 0,9 1 0,8 0,7 0,7 5185 ASTMD Ca mg/kg 40,1 40 39,1 30,4 27,6 26,2 5185 ASTMD Mg mg/kg 4,3 4,2 4,1 3,7 3,5 3,5 5185 ASTMD P mg/kg 67,5 64,5 64,5 61,8 57,5 57,4 5185 ASTMD Mn mg/kg <0,3 <0,3 <0,3 <0,3 <0,3 <0,3 5185 Excellent removal for PE and good removal of solid material by settling was observed.

Fairly good removal of Ca, Si, Fe, Mg and P was observed. PE, as well as solid material, P and metals were concentrated to the bottom between 1st and 3rd day.

Example 4 Bleaching of settled AF The bleaching flux of settled animal fat from Example 1 (sample from the middle of the ng vessel after 5 weeks) was improved compared to the original feed. The fat purification result was similar in both cases, r, the settled fat had <10 ppm PE (02995810) compared to 17 ppm in bleached original feed (02932479), cf. Fig. 3 Example 5 ent of sludge The sludge fraction of Example 1 was analyzed to contain an increased amount of phosphorus, metals and polyethylene (Table 5). However, this fraction contains also a large amount of oil, which could be taken back to the process after some treatment.

Table 5. Impurities in feed animal fat (0 weeks settling), sample from the middle of the settling vessel and sludge (5 weeks settling) from settling test.

SampIe ) Feed 82 Sludge (5 weeks) weeks) Oili 11 02949755 02965160 Fe 1,1 1,3 13,5 Na 53,4 57,5 123 Ca 42 22,9 535 Mg 4,4 3,7 30,2 P 67 52,4 412 Zn 1 - - N 480 500 500 PE 166 <10 5409 PHO 595 554 987 The sludge was treated in the following ways: The sludge was treated by acid ing which was able to remove large s of impurities (sample 02965166), however, not all polyethylene, which resulted in problems in the following bleaching test. Only ca. 50 g could be filtered in the Dahlman device before the filter was clogged (sample 02965844). The rest of the fat was therefore centrifuged after adsorption treatment instead of Dahlman filtration (sample 02967121) but PE is not removed fully in fugation. Results are presented in Table Table 6. Sludge treated with acid degumming followed by bleaching.

Feed sludge AT-W-C AT-W-C + AT- AT-W-C + AT- W-A—F W-A—C 1000 ppm ca + 3% 800 ppm ca + 800 ppm ca + 02% water /70 C (PEB) 02% water + water + 0,7% Tonsil 0,7% Tonsil (PEB) (PEB) Oili 02965160 02965166 02965844 02967121 Fe 13,5 0,7 <0,1 Na 123 2,4 <1 Ca 535 17,6 0,8 Mg 30,2 1,4 <0,3 P 412 30,6 3,8 N 500 380 350 - | PE | 5409 | 1100 NA. | 469 Filtration tion has been effective for PE removal of the feed animal fat (<1-2 ppm PE in samples), therefore this could be a possible ent for the sludge in order not to clog the bleaching unit.

Filtration of the sludge was possible through a 2 pm and 0.45 pm filter paper. A large amount of brown precipitate was collecting on the 2 pm paper. The large amount of precipitate made the filtration quite slow.

Heat treating (in a pressure reactor 240 °C/30 min) the sludge resulted in somewhat faster filtration. The precipitate was here also collecting on the 2 pm paper.

The amount of precipitate was in both cases around 3.5% of the original sludge, hence 96.5% of the sludge could be further taken back to e.g. bleaching.

It seems like settling removes phosphates from the al feed, however, not as effectively olipids. Also protein and polyethylene is found in the precipitate collected on the filter. The precipitate of the heat treated sludge did not contain protein and r any phospholipid, which have been ed by heating.

Table 7. Analysis results of precipitates collected on filter paper.

Precipitate from filtration of original Precipitate from filtration of Heat sludge treated sludge Oi" 02996372 02996373 Precipitate on filter (% of original sludge) 3-2 3-7 IR Alot of calcium phosphate. A lot of calcium phosphate orIg. sludge Quite a lot of protein and (hgwiegtréfss than mp p polyethylene (however, masked by ' long chains of glycerides). No n.

Quite a lot of polyethylene (however, masked by long chains of glycerides).

EDS C 55-82%, 0 21-31%, Ca 3%, P C 56-84%, 0 , Ca 3%, P 2%, Na <1%, Mg <1%, K <1% and 2%, Na<1%, Mg <1%jaK<1%. Zn <1%.

PGLY (mg/kg) <05 <05 PE (mg/k9) <05 <05 PI (mg/k9) 1040 <0,5 PC (mg/k9) 500 <0,5 PA (mg/kg) 200 <0,5 LPA ) 1600 <0,5 LPC (mg/kg) 1200 <0,5 SM ) 1000 <0,5 PHO (mg/kg) 5520 <0,5 other PHO (mg/kg) 480 <0,5 phospholipids of total P 1’2* <05 (PHO/P) % Total fatty acids (GC) 57 75 *Calculated based on 4.3% P in PHO, P in sample based on EDS-analysis. (EDS: energy dispers'V9 ometry).

Results for the filtered oil samples are presented in Table 8. tion could remove more sodium, phosphorus and zinc from the heat treated sludge than from the al.

Polyethylene was unfortunately not analyzed because of too small sample size.

Bleaching of the heat treated and filtered sludge could remove all metals and only 1.2 ppm P remained after Dahlman filtration (no polishing) (Table 8). The bleaching flux is presented in Figure 4.

Table 8. Filtration of original and heat treated sludge.

Feed Heat Filtration Filtration 0.45 sludge treatment um + AT—W-A—F 0.45 um/ 850 800 ppm ca + 02% water + 0,7% Tonsil (filtr. 100 C) Oili 2965160 N0 heat 02981183 Fe 135 treatment 22 Na 123 (origina' 59,7 SIUdge) Ca 535 21,7 Mg 30,2 3,6 P 412 52,4 Zn - 59,1 N 500 390 PE 5409 NA. ' Oili 2965160 Heat 2981181 2996346 Fe 135 treatment in 1 <0,1 Na 123 2713:; ""340 23,1 <1 Ca 535 26 <0,3 Mg 30,2 3,1 <0,3 P 412 24,4 1,2 Zn - 7 <0,5 N 500 410 430 PE 5409 NA. <1 Settling of AF containing PE can be used to remove >97% PE and additionally some metals, especially calcium, and orus. The ing flux of the fat improved with settling of PE and part of the impurities.

The settled sludge can thereafter be treated by filtration (or heat treatment and filtration) to remove large amounts of calcium phosphate and polyethylene which it contains. Ca. 96 % fat can be separated from the sludge which can be taken back to the s and purified by e.g. bleaching. Thus, sludge heat treatment followed by filtration and bleaching results in pure fat, containing only 1.2 ppm P and no PE.

Claims (15)

1. A method for purifying lipid material, wherein the method comprises the following steps; a) storing the lipid material in a settling tank at elevated temperature, 5 b) allowing the impurities to settle to the bottom of the settling tank to thereby form an oily sludge phase, c) separating the formed oily sludge phase from the rest of the lipid material, d) r processing the lipid material e) purifying said separated oily sludge phase from impurities, and optionally 10 f) returning the purified oil from the purifying step e) to said settling tank, wherein step e) comprises a heat ent step comprising the steps of; i. heating said oily sludge phase to a temperature of from about 150oC to about 300oC, ii. adding polar solvent to said oily sludge phase for l of 15 impurities from oil phase such as e.g. phosphorus or calcium compounds, and iii. separating and recovering purified oil and, wherein said elevated temperature in step a) is from about 40oC to about 120 oC.

2. The method according to claim 1, wherein settling in the settling tank takes place without any form of stirring.

3. The method according to claim 1 or 2, wherein the time during which the impurities 25 in the lipid material is allowed to settle to the bottom of the settling tank is from about 5 hours, about 10 hours, about 15 hours, about 1 day, about 2 days, about 3 days, about 4 days, about 5 days.

4. The method according to any one of the ing claims, wherein the lipid 30 material is ating from ical material.

5. The method according to any one of the preceding claims, wherein the lipid material is selected from used cooking oil, vegetable oils or any kind or animal fats of any kind or mixtures thereof. 5

6. The method according to any one of claims 1 to 3 or 5, n the lipid material is selected from any fossil based oil or product, various oils used and ed by the oil ry, fuel oils and gasoline (petrol), including all used products in either the refining s, or used lubrication oils, waste plastic pyrolysis oils and the likes.

7. The method according to any one of the preceding claims, wherein said separation step in step c) comprises phase separation by decantation, whereby the lipid material is separated from the oily sludge. 15

8. The method according to any one of the preceding claims, wherein the heating in step i) is med during a period of about 5 to about 60 minutes, or about 10 minutes to about 50 s, about 15 minutes to about 40 s, about 20 minutes to about 30 minutes. 20

9. The method according to any one of the preceding claims, wherein the heating in step i) is about 170oC to about 240oC, preferably about 180oC to about 200oC.

10. The method according to any one of the preceding claims, wherein the polar solvent is water, methanol or ethanol or any combination thereof.

11. The method according to any one of the preceding claims, wherein the recovered purified oil in step iii) is subjected to a tion and/or centrifugation and/or mechanical removal to remove impurities t in the sludge. 30

12. The method according to any one of the preceding claims, wherein the separated and recovered purified oil is further subjected to a bleaching step.

13. The method according to any one of the preceding claims, wherein impurities are one or more of polyethylene, calcium salts, sodium salts or phosphorous salts.

14. The method according to any one of the preceding claims wherein at least about 90 %, or at least about 95%, at least about 97%, at least about 98 %, at least about 99 % of the original content of polyethylene in the lipid material is removed. 5

15. The method according to claim 1, ntially as herein described with reference to any one of the Examples and/or