WO2022112592A1

WO2022112592A1 - New formulations with reduced antioxidant content, their manufacture and use

Info

Publication number: WO2022112592A1
Application number: PCT/EP2021/083524
Authority: WO
Inventors: Jochen Alexander BUTZ; Thomas Lindemann; Christos TSEKOU; Kai Urban; Christian Schaefer
Original assignee: Dsm Ip Assets B.V.
Priority date: 2020-11-30
Filing date: 2021-11-30
Publication date: 2022-06-02
Also published as: CN116583190A; EP4250959A1

Abstract

The present invention is directed to beadlets with a self-heating temperature ≥ 120°C comprising gelatin, lignosulfonate, a low amount of antioxidant, and Vitamin A or a derivative thereof and optionally Vitamin D or a derivative thereof, as well as to a container with a volume ranging from 450 l to 3000 l comprising such beadlets. The present invention is further directed to a process for the manufacture of such beadlets, their use as additive to feed and premixes and feed additives, premixes and feed comprising such beadlets.

Description

New formulations with reduced antioxidant content, their manufacture and use Summary of the invention The present invention is directed to a formulation, especially a solid formulation, with a self-heating temperature ≥ 120°C comprising a high amount of gelatin, a low amount of antioxidant, Vitamin A or a derivative thereof and optionally Vitamin D or a derivative thereof, as well as to a container with a volume of up to 3000 l comprising such formulation. The present invention is further directed to a process for the manufacture of such formulation, its use as additive to feed and premixes and feed additives, premixes and feed comprising such formulation. When the formulation is prepared according to the process as disclosed below, it is also called “beadlets”. It was a surprise that such formulation/beadlets with the advantageous properties as laid down below could be prepared with such low amounts of antioxidants. It was especially surprising that the self-heating temperature of such formula- tions/beadlets is increased though their antioxidant content is decreased compared to the formulations of the prior art. So far it was expected that an amount of at least 10 weight-% of an antioxidant such as e. g. BHT is needed to ensure a self-heating temperature of at least 120°C. Background of the invention Formulations with oxidation sensitive compounds such as fat-soluble vitamins, especially vitamin A, vitamin D and any derivatives and mixtures thereof, have a potential for oxidation processes already at ambient conditions while storing or transporting such formulations. Depending on the reaction velocity of such exothermic degradation processes, the storage or transport temperature and the volume of the stored or transported formulation, heat accumulation can result which may lead to self-heating and even auto-ignition of such formulations. To minimize the degradation processes and thus decreasing also the self-heating effect, the oxidation sensitive compounds have to be protected in a suitable matrix and form. Formulations of vitamin A, vitamin D and any derivatives and mixtures thereof having a self-heating temperature ≥ 100°C, but lower than 120°C have to be stored and transported in flexible intermediate containers with a volume of < 450 l. Furthermore, they have to be classified as “Dangerous goods class 4.2” and special equipment has to be used for their storage and transport which adds to the overall costs of such formulation. Formulations of vitamin A, vitamin D and any derivatives and mixtures thereof having a self-heating temperature ≥ 120°C (as measured as described below) are allowed to be stored and transported in containers, especially in flexible intermediate bulk containers (“FIBCs”), of volumes up to 3000 l (= 3 m³), preferably in containers, especially in FIBCs, of volumes ranging from 450 l to 3000 l. Furthermore, no classification as “dangerous goods” is needed. For reasons of sustainability it is highly desired to use such containers, especially such FIBCs, i.e. such bigger bags of volumes up to 3000 l compared to smaller bags of volumes < 450 l: First, because due to their larger size, less bags are needed to store and transport the same amount of formulation. Second, since the containers, especially the FIBCs, until now are not re-usable, less bags have to be discarded. Thus, there is the need to provide a formulation of vitamin A, vitamin A derivatives and any mixtures thereof and any of their mixtures with vitamin D which has a self- heating temperature ≥ 120°C so that it can be stored and transported in containers, especially in FIBCs, of volumes up to 3000 l, preferably in FIBCs of volumes ranging from 450 to 3000 l, more preferably in FIBCs of volumes ranging from 480 to 2000 l, even more preferably in FIBCs of volumes ranging from 500 to 1500 l and from 500 to 1000 l, most preferably in FIBCs of volumes ranging from 600 to 800 l. Detailed description Thus, this need is fulfilled by the present invention, which is directed to a formulation with a self-heating temperature ≥ 120°C comprising a) a fat-soluble vitamin in an amount of at least 25 weight-%, whereby the fat- soluble vitamin is vitamin A or a derivative thereof and optionally vitamin D or a derivative thereof; b) gelatin in an amount of at least 40 weight-%; c) lignosulfonate in an amount of at least 1 weight-%; d) at least one antioxidant in an amount of ≤ 7 weight-%; e) an anti-caking agent; f) optionally an oil; g) optionally a reducing sugar; h) optionally a polyhydric alcohol; i) optionally residual moisture; whereby all amounts a) to h) sum up to 100 weight-% and are based on the total weight of the amounts of a), b), c), d), e), f), g) and h) together. The amount of residual moisture is preferably at most 6 weight-%, more preferably at most 5 weight-%, even more preferably at most 3.5 weight-%, most preferably at most 2 weight-%, based on the total weight of the formulation, i.e. the total weight of a) to i). The minimum amount of moisture in the formulation is preferably 0.1 weight-%, based on the total weight of the formulation. When step E) of the process according to the present invention is performed the moisture content is lower than without step E) being performed. Though the amount of antioxidant is low in these formulations, they show a self- heating temperature ≥ 120°C. Furthermore, they show a good stability and a good homogeneity in premixes, as well as a high stability under feed pelleting conditions. Since the formulations according to the present invention show a self- heating temperature ≥ 120°C and a ΔT < 60 K, they can be transported in containers, especially in FIBCs (“flexible intermediate bulk container”), of volumes up to 3000 l, preferably in containers, especially in FIBCs, of volumes ranging from 450 l. to 3000 l. Determination of the self-heating temperature The tests are performed according to Norm E-15188 and VDI 2263 Part 1. The samples are placed in a cubic shaped wire basket (either 16 ml or 1000 ml) in the center of an oven. The temperature of the oven is measured at two spots and remains constant during the testing period (24 hours), i.e. so called “isoperibolic test”. The temperature probe for the sample is placed in the center of the sample. Then the sample temperature reaches a temperature being 2 K below the oven temperature the 24 hour testing period starts. When the temperature difference “ ΔT” between sample and oven is < 60 K, the test criteria according to UN Orange book “Manual of Tests and Criteria, 6^th revised edition, chapter 33.3, Division 4.2 is passed, and the sample is considered as being self-heating stable according to the present invention. When the temperature difference “ ΔT” between sample and oven is > 60 K, the sample is considered as undergoing spontaneous ignition or dangerous self- heating. As illustrated by the examples, the formulations of the present invention show a self-heating temperature ≥ 120°C and a ΔT < 60 K. Container Any kind of container with a volume up to 3000 l, preferably with a volume ranging from 450 to 3000 l, more preferably with a volume ranging from 480 to 2000 l, even more preferably with a volume ranging from 500 to 1500 l and from 500 to 1000 l, most preferably with a volume ranging from 600 to 800 l, may be used. A “flexible intermediate bulk container” (“FIBC”), “jumbo”, “bulk bag”, “super sack”, "tote bag", or "big bag", is an industrial container made of flexible fabric that is designed for storing and transporting dry, flowable products, such as sand, fertilizer, and feed additives. FIBCs are most often made of thick woven polyethylene or polypropylene, either coated or uncoated, and normally measure around 45–48 inches (114–122 cm) in diameter and varies in height from 100 to 200 cm (39 to 79 inches). Its capacity is normally around 1,000 kg or 2,200 lb, but the larger units can store even more. A bulk bag designed to transport one metric ton (0.98 long tons; 1.1 short tons) of material will itself only weigh 5–7 lb (2.3–5.0 kg). Transporting and loading is done on either pallets or by lifting it from the loops. Bags are made with either one, two or four lifting loops. The single loop bag is suitable for one man operation as there is no need for a second man to put the loops on the loader hook. Emptying is made easy by a special opening in the bottom such as a discharge spout, of which there are several options, or by simply cutting it open. In the present invention preferably a big bag with four lifting loops is used. Its volume preferably ranges from 480 to 2000 l, more preferably from 500 to 1500 l, even more preferably from 500 to 1000 l, most preferably from 600 to 800 l. A loading with 200 to 1500 kg of the formulation according to the present invention is preferred. More preferred is a loading with 300 to 1200 kg of the formulation according to the present invention. Most preferred is a loading with 500 to 900 kg of the formulation according to the present invention. Thus, the present invention is also directed to a big bag, especially to a big bag with 3 or more lifting loops such as e. g.4 lifting loops, having a volume ranging from 480 l to 2000 l and comprising a formulation according to the present invention with the preferences as given below. It is especially advantageous if the FIBC has an “inliner”, which protects its content from light, oxygen and water, as well as if it is a Type C FIBC. Openings at the top for loading and at the bottom for unloading are convenient. Therefore, such openings are preferably present. Such openings will be tightly closed during storage and transport. Formulation The formulation is described in more detail below. The essential ingredients and their amounts, as well as the ingredients being absent in the formulations are further disclosed. Essential ingredients Fat-soluble vitamin The term "fat-soluble vitamins" comprises for the purpose of the present invention vitamins A and/or D, the corresponding derivatives such as e.g. esters, especially C₁-C₂₀ alkyl esters, as well as any mixture thereof. “Vitamin D” means either Vitamin D₃ (cholecalciferol) or Vitamin D₂ (ergocalciferol) or both. “Vitamin D derivative” means any derivative of Vitamin D as for example 25- hydroxy vitamin D₃ (so-called “HyD”), 1,25-dihydroxy vitamin D₃ or 24,25-dihydroxy vitamin D₃. Especially preferred examples of fat-soluble vitamins are vitamin A, vitamin A acetate, vitamin A propionate, vitamin A butanoate, vitamin A palmitate, vitamin D₃ and 25-hydroxy-vitamin D, as well as any mixture thereof. More preferred are vitamin A acetate, vitamin D₃ and any mixture thereof. Most preferred the fat- soluble vitamin is vitamin A acetate or a mixture of vitamin A acetate and vitamin D3, preferably in a weight ratio of vitamin A acetate to vitamin D3 ranging from 1:1 to 100:1, more preferably ranging from 10:1 to 85:1. The amount of the vitamin A or its derivative thereof is chosen in such a way so that its final amount in the formulation is preferably in the range of from 25 to 58 weight-%, more preferably its final amount is in the range of from 28 to 55 weight- %, even more preferably its final amount is in the range of from 30 to 50 weight-% and from 32 to 48 weight-%, most preferably its final amount is in the range of from 33 to 46 weight-%, based on the total weight of a) to h). By disclosing these ranges any combination of any lower value with any other value to a range is also disclosed, i.e.28-58 weight-%, 30-48 weight-%, 25-46 weight-% etc. If a mixture of Vitamin A acetate and vitamin D3 is used, the amount of vitamin A acetate is as given above for the vitamin A derivative and the amount of vitamin D3 is chosen in such a way so that its final amount in the formulation is preferably in the range of from 0.01 to 10 weight-%, more preferably its final amount is in the range of from 0.05 to 5 weight-%, even more preferably its final amount is in the range of from 0.1 to 3.5 weight-%, most preferably its final amount is in the range of from 0.3 to 2.5 weight-%, based on the total weight of a) to h). By disclosing these ranges any combination of any lower value with any higher value to a range is also disclosed, i.e.0.01-5 weight-%, 0.05-10 weight-%, 0.1-5 weight-% etc. When vitamin D, preferably vitamin D₃, is present in the formulation of the present invention advantageously also an oil is present. Oil The oils can be from any origin. They can be natural, modified or synthetic. If the oils are natural they can be plant or animal oils. Thus, the term “oil” encompasses any vegetable oil or fat like corn oil, sunflower oil, soybean oil, safflower oil, rapeseed oil, peanut oil, palm oil, palm kernel oil, cotton seed oil, olive oil, coconut oil, canola oil, sesame oil, hazelnut oil, almond oil, cashew oil, macadamia oil, mongongo nut oil, pracaxi oil, pecan oil, pine nut oil, pistachio oil, sacha Inchi (Plukenetia volubilis) oil, walnut oil, as well as middle chain triglycerides (“MCT”) and any mixture thereof. Preferably corn oil, peanut oil, safflower oil or sunflower oil are used. The weight ratio of vitamin D to the oil is preferably ranging from 1:1 to 1:10, more preferably from 1:2 to 1:5. Gelatin Suitable gelatins are poultry gelatin, porcine gelatin, bovine gelatin and any mixture thereof, as well as fish gelatin and any mixture with the other gelatins. The gelatin is generally classified according to its Bloom value. There are two types of gelatins: Type A gelatin is obtained from acid processing of collagen. Type B gelatin is obtained from alkaline processing of colIagen. Bloom is a test to measure the strength of a gel of gelatin. The test determines the weight (in grams) needed by a probe (normally with a diameter of 0.5 inch) to deflect the surface of the gel 4 mm without breaking it. The result is expressed in bloom (grades). In general gelatins with a Bloom ranging from 0 to 300 may be used. Low bloom, medium bloom and high bloom gelatin are gelatins having a strength of less than about 120 Bloom (low Bloom), between about 120 and up to 200 Bloom (medium Bloom) or a strength of more than about 200 Bloom (high Bloom. Low bloom gelatin, preferably gelatin with Bloom ranging from 0 to <120, more preferably gelatin with 60-110 Bloom, even more preferably gelatin with 70-90 Bloom, most preferably gelatin with 80 Bloom, can be used as well as medium bloom gelatin, preferably gelatin with 120-160 Bloom, more preferably gelatin with 140 Bloom, and high Bloom gelatin, preferably gelatin with 200-300 Bloom, more preferably gelatin with 200-270 Bloom, even more preferably gelatin with 200-250 Bloom, most preferably gelatin with 200 Bloom. The amount of gelatin in the formulations of the present invention is chosen in such a way so that its final amount in the formulation is preferably at least 41 weight-%, based on the total weight of a) to h). The maximum amount of gelatin in the formulation may preferably be 70 weight-%, based on the total weight of a) to h). Compound c) : Lignosulfonate (s) The lignosulfonates present in the formulations according to the present invention are especially industrially produced products which contain lignosulfonates having the widest variety of cations. Sodium, calcium, magnesium and ammonium lignosulfonate are especially preferred. A formulation according to the present invention can contain a single lignosulfonate or a mixture of several lignosulfonates as ingredient c). Furthermore, the lignosulfonate present in the formulations according to the present invention can be part of an industrially produced product which contains further components in addition to the lignosulfonates. As is known, the biopolymer lignin occurs together with cellulose in plants, especially in wood. Wood, depending on the type, contains about 16 to 37 weight-% of lignin. Considered chemically, lignin consists of irregular polymers of methoxylated phenylpropane monomers (p-coumaryl alcohol, coniferyl alcohol, sinapyl alcohol etc.) having a molecular weight estimated to be at least 20 kD. In a first step in the production of cellulose the wood is decomposed, which is achieved in most cases by treatment with sulfite lyes at 125°-180°C. Thereby, the cellulose is liberated and the lignin is converted into a water-soluble derivative, lignosulfonate (also known as “sulfite lignin”). On a smaller scale, the decomposition of wood is also achieved by treating the wood with sodium hydroxide and disodium tetrasulfide (the “Kraft process”). The lignin obtained in this process is referred to as “Kraft lignin” or “sulfate lignin” and is not water-soluble at neutral pH. More recent processes for the production of cellulose use organic solvents e.g. alcohol, also mixed with water, for the decomposition of wood, and the thus-produced lignin is referred to as “organosolv lignin”. This form of lignin is likewise not water-soluble. At present, primarily lignosulfonates and Kraft lignins are commercially available. Frequently, after the decomposition of the wood, the cellulose is separated and the resulting lignosulfonate-containing solution is concentrated to about 50% solid content and sold in this form. Most producers also offer pulverous products which have been obtained by spray-drying the solutions, and these solid forms also contain various saccharides in considerable amounts in addition to lignin. Some producers manufacture lignin derivatives having a relatively high content of lignosulfonate(s) from the primary (crude) lignosulfonates by enzymatic removal of the saccharides and, if necessary, by purification, for example by ultracentrifugation. The Kraft lignins, which are also offered, can be sulfonated in order to achieve water- solubility and the sulfonation products are suitable as lignosulfonates for use in the preparations in accordance with the invention. Commercial lignosulfonate products typically consist of about 40—90% lignosulfonate and smaller amounts of various saccharides, ash, carbohydrates, acetates, formates, resins etc., with the composition depending very much on the quality of the wood which is used. Such water-soluble lignosulfonate products are also suitable for use in the feed additives in accordance with the invention. In general, not only the crude products having a relatively high content of saccharides and additional byproducts but also the aforementioned purified lignin derivatives can be used in the feed additives in accordance with the invention, provided that such lignin derivatives are water- soluble or at least water-dispersible. Preferred examples of well-suited lignin derivatives are: sodium lignosulfonate, ammonium lignosulfonate, magnesium and calcium lignosulfonate as well as any of their mixtures. Sodium lignosulfonate and calcium lignosulfonate are especially preferred. Most preferred is calcium lignosulfonate. Suppliers of lignosulfonates are: Borregaard Industries Limited, Norway; Burgo Group, Rayonier Advanced Materials, Wuhan Xinyingda Chemicals, Shenyang Xingzhenghe Chemical, Abelin Polymers, GREENAGROCHEM, Harbin Fecino Chemical, Karjala Pulp, Nippon Paper Industries, Pacific Dust Control, Sappi, The Dallas Group of America, Venki Chem and Xinyi Feihuang Chemical. Especially suitable de-sugared calcium lignosulfonate is available from Borregaard Industries Limited, Norway under the tradenames Borrebright CY22P, Borresperse Na220 and Borrement CA120, whereby Borrebright CY22P is especially preferred. This is manufactured by cutting spruce timer into chips and feeding it into a digester together with cooking calcium bisulfite solution. During the cooking at high temperature (130-140°C) the lignin in the wood is depolymerized and sulfonated, which makes water-solublelignosulfates. At the end of the cooking the sulfite liquor contains calcium lignosulfonate and sugars. The sulfite liquor (calcium lignosulfonate and sugars) is separated from the cellulose pulp by filtration. The sulfite lye is concentrated to about 53% in an evaporation plant. The concentrated liquor is fed into a spray dryer to produce lignosulfonate powder (inlet temperature in the range of from 200 to 250°C). The amount of the lignosulfonate(s) is chosen in such a way so that its final amount in the formulation is preferably in the range of from 1 to 10 weight-%, preferably in the range of from 1.5 to 6 weight-%, based on the total weight of a) to h). Reducing sugar Examples of suitable reducing sugars are aldohexoses and ketohexoses with a hydroxy group in α-position. Reducing disaccharides such as e.g. lactose and maltose and reducing oligosaccharides may also be used, as well as aldopentoses and ketopentoses with a hydroxy group in α-position. Preferred examples of reducing sugars are glucose, fructose, galactose and any mixture thereof. A suitable mixture of fructose and glucose is e.g. invert sugar. A further suitable reducing sugar mixture is high-fructose corn syrup (HFCS), also known as glucose-fructose, isoglucose and glucose-fructose syrup, a sweetener made from corn starch. "HFCS 42" and "HFCS 55" refer to 42% and 55% fructose composition respectively, the rest being glucose and water. Hydrolysed starch products with a DE > 20, so called “glucose syrups” or “dried glucose syrups” – depending on their water content, may also be used as reducing sugars. Glucose syrup 4280, i.e. a glucose syrup with a DE ranging from 42-80 is especially suitable. “Dextrose” is a synonym for “glucose”. The term “dextrose equivalent” (DE) denotes the degree of hydrolysis andis a measure of the amount of reducing sugar calculated as D-glucose based on dry weight; the scale is based on native starch having a DE close to 0 and glucose having a DE of 100. “Glucose syrups” or “dried glucose syrups” may be used in form of powders, micro- granulates or granulates. Glucose syrups consist in general of a mixture of glucose, maltose and oligo- and polysaccharides with varying amounts of these ingredients. When glucose syrup is used its amount is calculated on basis of the dried glucose syrup. More preferred examples are glucose, fructose and any mixture thereof. Even more preferred a single reducing sugar is used, especially either fructose or glucose or glucose syrup with a DE ≥ 50. Most preferred is fructose. The amount of the reducing sugar in the formulations of the present invention is chosen in such a way so that its final amount in the formulation is preferably in the range of from 0 to 5.0 weight-%, more preferably its final amount is in the range of from 1.0 to 4.5 weight-%, based on the total weight of a) to h). Polyhydric alcohol Examples of suitable polyhydric alcohols are glycerol, monoesters of glycerol with C_1-5monocarboxylic acids, monoethers of glycerol, diglycerol, triglycerol, polyglycerol, propylene glycol, dipropylene glycol, 1,3-butylene glycol, ethylene glycol, polyethylene glycol, sorbitol, xylitol, maltitol, erythritol, mannitol, etc. These polyhydric alcohols can be used alone or in a combination of two or more. Preferable examples of polyhydric alcohol include glycerol, sorbitol, xylitol, maltitol, erythritol, and mannitol, whereby glycerol is especially preferred. The amount of the polyhydric alcohol in the formulations of the present invention is chosen in such a way so that its final amount in the formulation is preferably in the range of from 0 to 5.0 weight-%, more preferably its final amount is in the range of from 0.1 to 2.5 weight-%, based on the total weight of a) to h). Antioxidant The antioxidant may be a water-soluble antioxidant or a fat-soluble antioxidant or any mixture thereof. Thus, mixtures of water-soluble antioxidants, mixtures of fat- soluble antioxidants and mixtures of one or more water-soluble antioxidants and one or more fat-soluble antioxidants are also included in the term “antioxidant”. Preferred are fat-soluble antioxidants as well as mixtures thereof and mixtures of water- and fat-soluble antioxidants. Inorganic antioxidants may also be present. Examples of inorganic antioxidants are NaBH₄, Na₂SO₃ and/or Na₂S₂O₃. Examples of fat-soluble antioxidants are ascorbyl palmitate, polyphenols, flavones being substituted with one or more hydroxy groups, isoflavones being substituted with one or more hydroxy groups, tocotrienols and analogues thereof, tocopherols and analogues thereof, phenols with bulky alkyl groups such as e.g. butylated hydroxyanisoles (“BHA”), butylated hydroxytoluenes (“BHT”), tert- butylhydroquinone, thymol (= 5-Methyl-2-(propan-2-yl)phenol), eugenol (= 2- Methoxy-4-(prop-2-en-1-yl)phenol) or any mixture thereof. Analogues of tocopherols and tocotrienols are especially compounds with a shorter side chain in position 2 compared to tocopherols and tocotrienols. Examples of flavones substituted with one or more hydroxy groups are: 6- hydroxyflavone, 5,7-dihydroxyflavone (= chrysin), 4',5,7-trihydroxyflavone (= apigenin), 3',4',5,7-tetrahydroxyflavone (luteolin) and 4',5,6,7,8-pentamethoxy- flavone (tangeritin). Examples of isoflavones substituted with one or more hydroxy groups and optionally methoxy groups are daidzein (= 4’,7-dihydroxyisoflavone), genistein (= 4',5,7-trihydroxyisoflavone), prunetin (=4',5-dihydroxy-7-methoxyisoflavone), biochanin A (= 5,7-dihydroxy-4’-methoxy-soflavone), orobol (= 3’,4’,5,7- tetrahydroxyisoflavone), santal (= 3’,4’,5-trihydroxy-7-methoxy-isoflavone) and pratensein (= 3’,5,7-trihydroxy-4’-methoxyisoflavone). The BHA is preferably a mixture of 2-tert-butyl-4-hydroxy-anisole and 3-tert-butyl- 4-hydroxy-anisole. The BHT is preferably 2,6-di-tert-butyl-p-cresol (IUPAC name = 2,6-di-tert-butyl-4-methylphenol). The use of BHA is restricted; it is e.g. not allowed in cat food any more. Thus, it is not a preferred antioxidant in the formulation of the present invention. Examples of water-soluble antioxidants are ascorbic acid and its salts such as e.g. sodium ascorbate, citric acid and its salts such as e.g. sodium citrate, as well as any mixture thereof. Preferred examples of mixtures of water- and fat-soluble antioxidants are tocopherol and sodium ascorbate, tocopherol and ascorbic acid, whereby the tocopherol may be alpha-, beta-, gamma- or delta-tocopherol, preferably whereby the tocopherol is alpha- or delta-tocopherol, more preferably whereby the tocopherol is alpha-tocopherol, most preferably whereby the tocopherol is DL- alpha-tocopherol. Tocopherols, tocotrienols and analogues thereof Examples of suitable tocopherols and analogues thereof are e.g. compounds of formula (II)

wherein R^1a and R^2a are independently from each other H or C_1-11-alkyl or (CH₂)_n─OH with n being an integer from 1 to 4, or R^1a and R^2a represent together a keto group, A is CHR^3a or C(=O), and wherein R^3a, R^4a and R^6a are independently from each other H or C_1-4-alkyl, and wherein R^5a is H or OH or C_1-4-alkyl or C_1-4-alkoxy, as disclosed in WO 2019/185894. Further suitable tocopherols are compounds of formula (II), wherein one of the two substituents R^1a and R^2a is C_12-21-alkyl and the other of the two substituents R^1a and R^2a is either hydrogen or C_1-5-alkyl or (CH₂)_n-OH with n being an integer from 1 to 5, and wherein A is CH(R^3a), and wherein R^3a, R^4a and R^6a are independently from each other H or C_1-4-alkyl, and wherein R^5a is H or OH or C_1-4-alkyl or C_1-4-alkoxy, as disclosed in WO 2019/185938. Compounds of formula (II), wherein A is CH₂, R^1a is C_1-5-alkyl, R^2a is either H or C_1-2- alkyl, R^5a is either H or C_1-4-alkoxy or C_1-4-alkyl, and R^4a and R^6a are independently from each other either H or C_1-4-alkyl, with the preferences as disclosed in WO 2019/185900 are also suitable antioxidants in the formulations of the present invention. Preferred examples of the antioxidants of formula (II) as disclosed in WO 2019/185894 are the following compounds of formula (1)-(11) with “Me” being methyl:

Further examples of suitable antioxidants that can be used in the formulations of the present invention are compounds of formula (III) and (IV),

wherein R^1b and R^2b are independently from each other H or C_1-11-alkyl or (CH₂)_n─OH with n being an integer from 1 to 6 or R^1b and R^2b together represent a keto group, and wherein R^3b, R^4b, R^5b, and R^6b are independently from each other H or C_1-6-alkyl or C_1-6-alkoxy, and R^7b is H or C_1-6-alkyl, as disclosed in WO 2019/185898. “alkyl” and “alkoxy” hereby encompass linear alkyl and branched alkyl, and linear alkoxy and branched alkoxy, respectively. Preferred examples of compounds of formula (III) and (IV) are the following compounds (12)-(19):

Further suitable antioxidants are compounds of formula (V), whereby R¹, R² and R³ are independently from each other H or linear C_1-6-alkyl or branched C_3-8-alkyl, whereby preferably R¹ is H or methyl or ethyl or n-propyl or iso-propyl or tert-butyl and R² and R³ are independently from each other H or methyl or ethyl, with the further preferences as disclosed in WO 2019/185940.

Also, the compounds of formula (VI) with n being 1 or 2, R^1b and R^3b being independently from each other H or C_1-5-alkyl, and R^2b being either H or C_1-5-alkyl or C_1-5-alkyloxy, preferably with the proviso at least one of R^1b, R^2b and R^3b being H, as disclosed in WO 2019/185904 can be used as antioxidants in the formulations of the present invention.

Hereby the following compounds of formulae (VI-1) and (VI-2) are especially preferred:

The asterisks * mark each a chiral/stereogenic center, i.e. all possible isomers having any configuration at said centers are encompassed by the term “compound of formula (VI-1)” and “compound of formula (VI-2)”, respectively. Also, suitable antioxidants are compounds of the following formulae (VII) and (VIII) with R^1c, R^2c and R^3c being independently from each other H or C_1-4-alkyl as published in WO 2019/185942 and WO 2019/185888, respectively. Preferred examples thereof are tocotrienols and tocopherols of the formulae (20) to (27) as shown below

The asterisks * mark each a chiral/stereogenic center. The term “compound of formula (VII)/(VIII)” encompasses all possible isomers having any configuration at said centers. Especially preferred examples of the compound of formula (VII) are the following compounds of formulae (20) (= alpha-tocotrienol), (21) (= beta-tocotrienol), (22) (= gamma-tocotrienol) and (23) (= delta-tocotrienol), whereby all possible diastereomers and enantiomers are included.

Especially preferred examples of the compound of formula (VIII) are the following compounds of formulae (20) (= alpha-tocopherol), (21) (= beta-tocopherol), (22) (= gamma-tocopherol) and (23) (= delta-tocopherol), whereby all possible diastereomers and enantiomers are included.

The asterisks * mark each a chiral/stereogenic center. The term “compound of formula (20)/(21)/(22)/(23)/(24)/(25)/(26)/(27)” encompasses all possible isomers having any configuration at said centers. Polyphenols Examples of suitable polyphenols are 2,4,5-trihydroxybutyrophenone, epigallo- catechin gallate (“EGCG”), epigallo-catechin, gallo-catechin, hydroxytyrosol, resveratrol, carnosol, 2-(3,4-dihydroxyphenyl)acetic acid and C_1-6 alkyl esters thereof, and any mixture thereof. Further suitable polyphenols are derivatives, preferably esters and (earth) alkali metal salts, of hydroxybenzoic acids such as e.g. gallic acid (= 3,4,5-trihydroxybenzoic acid) and syringic acid (= 4-hydroxy-3,5-dimethoxy-benzoic acid). Examples of preferred esters are C1-20 alkyl esters of gallic acid such as e.g. propyl gallate, octyl gallate or dodecyl gallate, and C_1-20 alkyl esters of syringic acid. Also, derivatives, preferably esters and (earth) alkali metal salts, of cinnamic acid and hydroxycinnamic acids such as e.g. ferulic acid (= 3-(4-hydroxy-3- methoxyphenol)prop-2-enoic acid), caffeic acid (= 3,4-Dihydroxycinnamic acid), dihydrocaffeic acid (= 3-(3,4-dihydroxyphenyl) propanoic acid), chlorogenic acid (= the ester of caffeic acid and (−)-quinic acid), o-, m-, p-coumaric acid (= 2-/3-/4- hydroxycinnamic acid), rosmarinic acid (= a caffeic acid ester of 3-(3,4- dihydroxyphenyl)lactic acid), or sinap(in)ic acid (= 3,5-dimethoxy-4-hydroxycinnamic acid) may be used as antioxidants in the present invention. Examples of derivatives of cinnamic acid are Z-ethoxyethyl p-methoxycinnamate, ethylhexyl p-methoxycinnamate, 2-ethylhexyl 4-methoxycinnamate, methyl diiso- propylcinnamate, isoamyl 4—methoxycinnamate, and diethanolamin 4-methoxy- cinnamate. The most preferred antioxidants used in the formulation of the present invention are a butylated hydroxytoluene (= “BHT”) such as 2,6-di-tert-butyl-p-cresol (IUPAC name = 2,6-di-tert-butyl-4-methylphenol) as well as a mixture of DL-alpha- tocopherol and sodium ascorbate, a mixture of DL-alpha-tocopherol and ascorbic acid and a mixture of DL-alpha-tocopherol and ascorbyl palmitate. The weight ratio of DL-alpha-tocopherol to sodium ascorbate and of DL-alpha- tocopherol to ascorbic acid is preferably ranging from 5:1 to 1:5, more preferably from 3:1 to 1:3, even more preferably from 2:1 to 1:2, most preferably from 1.1:1 to 1:1.1. Surprisingly the total amount of the antioxidant(s) in the formulations of the present invention is lower than in gelatin-based formulations already being on the market. Preferably the total amount of the antioxidant(s) is chosen in such a way so that its/their final amount in the formulation is preferably ≤ 4.0 weight-%, more preferably its/their final amount is in the range of from 0.1 to 3.0 weight-% and from 0.2 to 2.5 weight-%, based on the total weight of a) to h). Anti-caking agent Suitable organic anti-caking agents are corn starch, as well as starches from other botanical sources such as e.g. as waxy corn, wheat, tapioca, pea and potato, as well as derivatives thereof such as pre-gelatinised starch, starch ethers (e.g. carboxymethyl starch), starch esters (e.g. starch monophosphate, alkenyl- succinated starch, especially octenyl-succinated starch), cross-linked starch and oxidized starch and any mixture thereof. Other suitable organic anti-caking agents are talc, cellulose, microcrystalline cellulose, cellulose derivatives or fibres, ferric ammonium citrate, sodium salts of fatty acids such as e.g. sodium stearate, potassium salts of fatty acids such as e.g. potassium stearate, calcium salts of fatty acids such as e.g. calcium stearate, magnesium salts of fatty acids such as e.g. magnesium stearate, aluminum salts of fatty acids such as e.g. aluminum stearate, ammonium salts of fatty acids such as e.g. ammonium stearate, and any mixture of any of them. Other suitable anti-caking agents are inorganic anti-caking agents such as e.g. silicic acid H_2n+2Si_nO_3n+1 and alkaline/earth alkali metal salts thereof, precipitated silicic acid, silica (= silicon dioxide), modified silica, hydrophobically modified silica, precipitated silica, magnesium oxide, dicalcium diphosphate, tricalcium phosphate, magnesium phosphate, sodium carbonate, potassium carbonate, calcium carbonate, magnesium carbonate, calcium oxide, magnesium oxide, potassium silicate, calcium silicate, magnesium silicate, magnesium trisilicate, aluminum silicate, sodium aluminum silicate, potassium aluminum silicate, calcium aluminum silicate, zeolithe (aluminosilicates), disodium sulfate or mixtures thereof. Further suitable inorganic anti-caking agents are bentonite and kaolin. Also, mixtures of organic and inorganic anti-caking agents may be used. The preferred anti-caking agents used in the formulations of the present invention are anti-caking agents with a particle size D(v,50%) from 100 nm to 10 μm, preferably from 100 nm to 9 μm, more preferably from 150 nm to 5 μm, measured as dry dispersion with a Malvern MasterSizer 3000 (laser diffraction). The particle size of the anti-caking agent can be determined with a laser diffraction system e.g. Malvern MasterSizer 3000, either as dry dispersion or as wet dispersion in oil or Volasil (a mixture of volatile and cyclic silicones such as octamethylcyclo- tetrasiloxane and decamethylcyclopentasiloxane). The particle size can also be determined with electron microscopy. The more preferred anti-caking agents are silicic acid H_2n+2Si_nO_3n+1, silica, microcrystalline cellulose, as well as any mixture thereof. The most preferred anti-caking agents are hydrophilic precipitated silicic acid H_2n+2Si_nO_3n+1, hydrophilic precipitated silica and any mixture thereof. The amount of the anti-caking agent is chosen in such a way so that its final amount in the formulation is preferably ranging from 1-10 weight-%, more preferably ranging from 3 to 9 weight-%, most preferably ranging from 4.5 to 7.5 weight-%, based on the total weight of a) to g). By disclosing these ranges any combination of any lower value with any higher value to a range is also disclosed, i.e.1-7.5 weight-%, 4.5-10 weight-% etc. Not present ingredients In contrast to the formulations disclosed in EP 494417 A2 the matrix of the formulations of the present invention does not comprise any of the following salts: water-soluble salts of carboxylic acids, sodium carbonate, potassium carbonate, calcium sulfate, and calcium phosphate. Examples of such water-soluble salts of carboxylic acids not being present in the matrix of the formulations of the present invention are: aluminum subacetate, sodium tartrate, sodium glutarate, sodium acetate, calcium acetate, sodium propionate, calcium propionate and sodium benzoate. Some of these salts may, however, be used as anti-caking agents during drying of the formulation, especially during the powder-catch process step. Preferably none of these salts is used in the manufacture of the formulations of the present invention; thus, the formulations of the present invention do not comprise any of these salts; i.e. no water-soluble salts of carboxylic acids, no sodium carbonate, no potassium carbonate, no calcium sulfate, and no calcium phosphate. In EP-A 494417 these salts are used for the cross-linking of the gelatin with a reducing sugar at temperatures ranging from 55°C to 85°C for 2-24 hours which was believed to be necessary for stable formulations. The process of the present invention has the advantage that no organic solvent except water is used, so that the formulation according to the present invention is substantially free of organic solvents. “substantially free” means that the amount thereof is ≤ 5 weight-%, preferably ≤ 3 weight-%, more preferably ≤ 1 weight-%, even more preferably ≤ 0.5 weight-%, most preferably ≤ 0.1 weight-%. The formulation of the present invention does preferably not comprise any non- reducing sugars such as e.g. sucrose instead of the reducing sugars. Mixtures of non-reducing and reducing sugars may, however, be used. Furthermore, no cross-linking agents such as e.g. acetaldehyde, glutaraldehyde or glyoxal are present in the formulations of the present invention. Ethoxyquin, also known as “EMQ” (IUPAC name: 6-Ethoxy-2,2,4-trimethyl-1,2- dihydroquinoline), is also not present in the formulations of the present invention; whereas according to EP-A 494417 the presence of ethoxyquin is necessary to obtain stable formulations. In a preferred embodiment of the present invention the formulation does not comprise ethoxyquin and it does not comprise a water-soluble salt of carboxylic acids and it does not comprise sodium carbonate and it does not comprise potassium carbonate and it does not comprise calcium sulfate and it does not comprise calcium phosphate. In a further preferred embodiment of the present invention the formulation does not comprise any of the compounds mentioned in this chapter “not present ingredients”. Characteristics of the formulations of the present invention The formulations of the present invention show preferably a bulk density ranging from 0.55-0.67 g/cm³, more preferably a bulk density ranging from 0.6-0.7 g/cm³. Furthermore, the formulations of the present invention show preferably a tap density ranging from 0.6-0.7 g/cm³. The bulk density and the tap density are measured as follows: A 250 ml glass cylinder is filled with the sample. The volume and the weight are measured. Bulk density is the weight divided by the volume. For measuring the tap density the sample is tapped with a 2000 Taps with a Stampfvolumeter JEL STAV II (J. Engelsmann AG). The tapped volume is measured. Tap density is the weight divided by the tapped volume. Preferably the formulations of the present invention show besides the bulk density and/or tap density above, also the particle sizes and/or particle size distribution as cited below, which results in a very good homogeneity when mixed into feed. Preferred embodiments of the formulations of the present invention Especially preferred formulations of the present invention are the following formulations A to C, whereby the amounts of the single ingredients are given in weight-%. The formulations preferably only contain the ingredients cited in the corresponding tables and no further ingredients. Thus, the formulations preferably consist only of the ingredients as cited in the corresponding tables. Instead of Vitamin A acetate another Vitamin A C_1-20 alkyl ester, preferably another Vitamin A C_2-16 alkyl ester, may also be used. Formulation A: All amounts are given in weight-% and are based on the total weight of the formulation

Any combination of the amount of one ingredient with the preferred amount of another ingredient and/or the more or most preferred amount of a further ingredient is also encompassed within the scope of this preferred Formulation A. If Vitamin D3 is additionally present in the Formulation A, its amount is in the range of 2-3 weight-%, based on the total weight of the ingredients cited in the corresponding table above. Furthermore, preferably also an oil is then present with the preferences as given above. In this case the amount of gelatin is reduced accordingly. Formulation B: All amounts are given in weight-% and are based on the total weight of all ingredients cited in the following table. Additionally, moisture in the amount as given above may be present.

Any combination of the amount of one ingredient with the preferred amount of another ingredient and/or the more or most preferred amount of a further ingredient is also encompassed within the scope of this preferred Formulation B. If Vitamin D3 is additionally present in the Formulation B, its amount is in the range of 2-3 weight-%, based on the total weight of the ingredients cited in the corresponding table above. Furthermore, preferably also an oil is then present with the preferences as given above. In this case the amount of gelatin is reduced accordingly. Formulation C: All amounts are given in weight-% and are based on the total weight of all ingredients cited in the following table. Additionally, moisture in the amount as given above may be present.

Any combination of the amount of one ingredient with the preferred amount of another ingredient and/or the more or most preferred amount of a further ingredient is also encompassed within the scope of this preferred Formulation C. If Vitamin D3 is additionally present in the Formulation C, its amount is in the range of 2-3 weight-%, based on the total weight of the ingredients cited in the corresponding table above. Furthermore, preferably also an oil is then present with the preferences as given above. In this case the amount of gelatin is reduced accordingly. Particle size and measurement To determine the particle size of the solid formulation of the present invention a sieve test can be performed with filters of 850 μm pores (mesh 20), 425 μm pores (mesh 40) and 150 μm pores (mesh 100). Furthermore, the particle size of the solid formulation may also be determined by laser diffraction analytic whereby the dry dispersion of the sample is measured with a Malvern Mastersizer 2000 or 3000 and Fraunhofer calculation. The particle sizes of the formulation, when determined with laser diffraction with a Malvern Mastersizer 3000 and Fraunhofer calculation, are as follows: D(v,10%) = 130-210 μm; D(v, 50%) = 220-300 μm; D(v, 90%) = 340-430 μm. Synonyms of “D(v,10%)” are “d(v,10%)”, “d(v,10)”, “d(v,0.1)”, “D(v,10)” and “D(v,0.1)”. This applies in an analogous manner for “D(v,50%)” and “D(v,90%)”. Process for the manufacture of the formulation The present invention is also directed to a process for the manufacture of a formulation with the preferences as cited above comprising the following steps: A) Dissolving gelatin b), the lignosulfonate c), and, if present, a water-soluble antioxidant d) in water to obtain a matrix; B) Heating the fat-soluble vitamin a), the fat-soluble antioxidant d) and, if present, an oil f) to obtain an active phase; C) Emulsifying the active phase obtained in step B) into the matrix obtained in step A) to obtain a dispersion; D) Spray-drying the dispersion obtained in step C) in presence of an anti-caking agent to obtain the formulation; whereby a reducing sugar g) and/or a polyhydric alcohol h) may optionally be added, preferably either to the matrix in step A) or in step C). Preferably the process for the manufacture of the formulation according to the present invention does neither comprise a crosslinking step performed by exposure to radiation nor does it comprise a crosslinking step performed by using an enzyme. The formulation of the present invention is preferably manufactured according to a process comprising the following steps: A) Dissolving gelatin b), the lignosulfonate c), the reducing sugar g), the polyhydric alcohol h) and, if present, a water-soluble antioxidant d) in water to obtain a matrix; B) Heating the fat-soluble vitamin a), the fat-soluble antioxidant d) and, if present, an oil f) to obtain an active phase; C) Emulsifying the active phase obtained in step B) into the matrix obtained in step A) to obtain a dispersion; D) Spray-drying the dispersion obtained in step C) in presence of an anti- caking agent e) to obtain the formulation. Alternatively, one or two of the two ingredients, the reducing sugar g) and the polyhydric alcohol h), may not be added to the water or matrix formed by the gelatin and the lignosulfonate in water in step A), but to the mixture in step C) before or during emulsification. The single steps are disclosed in more detail below. Further details, that may also be generalized, are given in the examples. Step A) The amounts of the gelatin b), the lignosulfonate c), the reducing sugar g), the polyhydric alcohol h) and if present, the water-soluble antioxidant d) are chosen so that the final amounts of these compounds in the solid formulation after having performed steps A) to D) and A) to E), respectively, is as described above. Step A) is preferably performed at a temperature ranging from 40 to 80°C, more preferably ranging from 50 to 75°C, most preferably ranging from 55 to 70°C. Step B) The amounts of the fat-soluble vitamin a), the fat-soluble antioxidant d) and, if present, the oil f) are chosen so that the final amounts of these compounds in the solid formulation after having performed steps A) to D) and A) to E), respectively, is as described above. Step B) is preferably performed at a temperature to bring the components a) and c) into a liquid state. When vitamin D, preferably vitamin D₃, is present in the formulation of the present invention, the vitamin D is preferably added to the other fat-soluble vitamin and the fat-soluble antioxidant as oily suspension, whereby the weight ratio of vitamin D to the oil is preferably ranging from 1:1 to 1:10, more preferably from 1:2 to 1:5. If only vitamin D, preferably vitamin D₃, is present in the formulation of the present invention, the vitamin D is preferably added to the fat-soluble antioxidant as oily suspension, whereby the weight ratio of vitamin D to the oil is preferably ranging from 1:1 to 1:10, more preferably from 1:2 to 1:5 Step C) Preferably this step is performed at a mixing temperature in the range of from 40 to 75°C, more preferably at a mixing temperature in the range of 50 to 70°C, even more preferably at a mixing temperature in the range of 55°C to 65°C to obtain a dispersion. The homogenization can be achieved by using a rotor-stator device or a high- pressure homogenizer or both. Other devices known to the person skilled in the art may also be used. Step D) The dividing and drying of the mixture of the oil-in-water preparation to produce the solid formulation according to the present invention can be done in any conventional way, such as spray cooling, modified spray cooling, spray drying, spray-drying in combination with fluidized bed granulation, modified spray drying or sheet drying and crushing, see e.g. WO 91/06292 A1. Preferably the conversion to the solid formulation is achieved by a powder-catch technique, whereby the sprayed dispersion droplets are caught by the anti-caking agent (so-called “catch media”), and dried. Step E) It is advantageous to treat the powder obtained after having performed step D) thermally. Hereby preferably temperatures of up to 125°C are applied, more preferably the thermal treating is carried out at a temperature ranging from 80- 120°C, even more preferably the thermal treating is carried out at a temperature ranging from 100 to 120°C, most preferably the thermal treating is carried out at a temperature ranging from 110 to 120°C. Hereby the amount of moisture in the formulation is decreased. Further embodiments of the present invention Use The present invention is also directed to the use of the formulation according to the present invention with the preferences as given above as additive to feed or premixes. Feed additive, premix and feed according to the present invention The present invention is also directed to a feed additive, a premix and a feed comprising the formulation according to the present invention with the preferences as given above. Feed (or ‘feedingstuff’) means any substance or product, including additives, whether processed, partially processed or unprocessed, intended to be used for oral feeding to animals. Feed in the context of the present invention is especially feed for broilers including starter, grower, finisher; broiler breeders including starter, grower (pullets), layers and male breeders, for layers and other poultry such as e.g. hens and duck layers, layers breeders, ducks and geese, partridges, quails and pheasants, ostrich and emu, for turkeys including starter, grower, finisher; for turkey breeders including starter, grower, layers and male breeders, for ruminants including calves, milk replacer, heifers, beef cattle, breeding bulls, sheep and goats; for horses, especially foals, leisure horses, race horses, mares and stallions, for rabbits, for mick and foxes, for swine including fattening pigs: pre-starter, starter, grower, finisher; breeders: replacement gilts, sows, boars, and feed for companion animals, especially for dogs and cats. The amount of the formulation and the fat-soluble vitamin respectively follows the regulatory guidelines in the regions depending on the specific animal species and its age. In the Supplementation Guidelines the amount of the vitamins A and D₃ is given in International Units (“I.U.”). To ensure that the active content in the feed is communicated in a systematic way, “I.U.” is used as a universal unit for fat soluble vitamins because there are different forms of the vitamins with varying amounts of fat-soluble vitamins. The formulation according to the present invention is usually added to feed in form of a premix, i.e. a mixture with other micro-nutrients such as other vitamins or their formulations and minerals. The premix inclusion in feed is < 1 weight-% for many species. The amount of the formulation according to the present invention needed to be included into the feed is calculated based on the active content of the feed and the targeted dosage of the fat-soluble vitamin in the final feed considering said inclusion level. The conversion factors of the fat-soluble vitamins are as follows: 1 I.U. Vitamin A corresponds to 0.344 μg of Vitamin A acetate; 1 I.U. Vitamin D₃ corresponds to 0.025 μg of Vitamin D₃. The following Table IV shows the amounts of the fat-soluble vitamins added per kg of air-dry feed. The exact amount is depending on several factors such as phase/age of the animal, animal species and legal local limits. Table IV

Below are given non-limiting examples of feed to which the formulations of the present invention may be added. Feed for poultry The feed for poultry differs from region to region. In the following Tables V and VI typical examples for diets in Europe and Latin America are given. These diets include cereals such as wheat, rye, maize/corn, minerals such as NaCl, vegetable oils such as soya oil, amino acids and proteins. Thus, the present invention is also directed to feed for poultry comprising the formulation according to the present invention; preferably to feed for poultry comprising the formulation according to the present invention and cereals, minerals, vegetable oils, amino acids and proteins. Table V: European diet

Table VI: Latin American diet

Pet food Pet foods are formulated to meet nutrient specifications using combinations of multiple ingredients to meet the targeted nutrient specification. The nutrient specifications for a complete and balanced dog or cat food will meet or exceed the guidelines provided by AAFCO (American Association of Feed Control Officials). The ingredient composition of pet-food can include any legal feed ingredient so number of combinations are not quite infinite but close. Some examples of ingredient used in dog and cat foods can be found in Table VII below: Table VII:

Thus, the present invention is also directed to pet food comprising the formulation according to the present invention; preferably to pet food comprising the formulation according to the present invention and animal meals and/or fresh meats, vegetable proteins, grains, fiber sources, fats and/or oils, micronutrients, palatants and optionally other non-basic ingredients. Feed for Swine Reference is made here to the NATIONAL SWINE NUTRITION GUIDE, 2010, whereby two non-limiting examples are given below. Table VIII: Corn and Soybean Meal Diet

Table IX: High fiber ingredient diet

Thus, the present invention is also directed to feed for swine comprising the formulation according to the present invention; preferably to feed for swine comprising the formulation according to the present invention and corn, soybean meal, minerals, vegetable oils, amino acids, further vitamins and trace mineral premixes. The invention is now further illustrated in the following non-limiting examples. Examples The following examples 1-5 illustrate the manufacture of the formulations of the present invention. Examples 1-5 General procedure I The matrix components, i.e. reducing sugar (if present), glycerol (if present), gelatin, lignosulfonate and optionally the water-soluble antioxidant are dissolved in water at approximately 65°C to obtain the “matrix”. Vitamin A acetate, Vitamin D3 (if present), oil (if present) and the fat-soluble antioxidant are heated at approximately 65°C under stirring until complete melting of vitamin A acetate (“active phase”). They are then emulsified into the matrix. Hereby, the amounts of the ingredients are chosen in such a way that their concentrations in the final formulation are as disclosed in Table 1, Table 2 and Table 3. After thorough mixing, the resulting dispersion is sprayed into a spray tower in the presence of an anti-caking agent to form droplets of the desired size. The solidified droplets are then dried by an drying air of various temperatures (5-75°C). The dried powder is separated from the majority of the anti-caking agent and sieved through 150 μm and 600 μm filters. The powder is further treated at a temperature of up to 120°C in a mixer or in a fluid bed, whereby it is made partially water-insoluble. The particle size of the dried and thermically-treated powder is determined with laser diffraction analytic with a Malvern Mastersizer 3000. The sample is hereby dry dispersed. By applying the Fraunhofer theory the particle size distribution of the sample is calculated. Furthermore, the bulk and the tap density are measured as described above. The self-heating temperature is determined according to the procedure as described above.

Table 1: Example 1 In the table all amounts are given in weight-% and are based on the total weight of the formulation. The amounts of all ingredients sum up to 100 weight-%.

Table 2: Example 2 In the table all amounts are given in weight-% and are based on the total weight of the formulation excluding the residual moisture. The amounts of all ingredients except the residual moisture sum up to 100 weight-%. The amount of residual moisture is based on the total weight of the formulation.

Table 3: Examples 3-5 In the table all amounts are given in weight-% and are based on the total weight of the formulation excluding the residual moisture. The amounts of all ingredients except the residual moisture sum up to 100 weight-%. The amount of residual moisture is based on the total weight of the formulation.

WDO = water-dispersible oil

Claims

Claims 1. A formulation with a self-heating temperature ≥ 120°C, whereby said formulation comprises a) a fat-soluble vitamin in an amount of at least 25 weight-%, whereby the fat- soluble vitamin is vitamin A or a derivative thereof and optionally vitamin D or a derivative thereof; b) gelatin in an amount of at least 40 weight-%; c) lignosulfonate in an amount of at least 1 weight-%; d) at least one antioxidant in an amount of ≤ 7 weight-%; e) an anti-caking agent; f) optionally an oil; g) optionally a reducing sugar; h) optionally a polyhydric alcohol; i) optionally residual moisture; whereby all amounts a) to h) sum up to 100 weight-% and are based on the total weight of the a), b), c), d), e), f), g) and h) together, and whereby preferably ethoxyquin is not present in the formulation.

2. The formulation according to claim 1, whereby the formulation does not comprise the following salts: water-soluble salts of carboxylic acids, sodium carbonate, potassium carbonate, calcium sulfate, and calcium phosphate, whereby the water-soluble salts of carboxylic acids not being present in the formulation are preferably: aluminum subacetate, sodium tartrate, sodium glutarate, sodium acetate, calcium acetate, sodium propionate, calcium propionate and sodium benzoate.

3. The formulation according to claim 1 and/or 2, whereby the amount of gelatin is at least 41 weight-%, based on the total weight of a) to h).

4. The formulation according to any one or more of the preceding claims, whereby said formulation has a bulk density ranging from 0.6 to 0.7 g/cm³.

5. The formulation according to any one or more of the preceding claims, wherein the formulation has a particle size D(v,50%) ranging from 200 to 300 μm, measured as dry dispersion with a Malvern MasterSizer 3000 (laser diffraction).

6. The formulation according to any one or more of the preceding claims, wherein said anti-caking agent d) has a particle size D(v,50%) ranging from 100 nm to 10 μm, measured as dry dispersion with a Malvern MasterSizer 3000 (laser diffraction).

7. The formulation according to any one or more of the preceding claims, wherein the fat-soluble vitamin a) is vitamin A acetate or a mixture of vitamin A acetate and vitamin D3, preferably in a weight ratio of 1:1 to 100:1, more preferably from 10:1 to 85:1

8. The formulation according to any one or more of the preceding claims, whereby said antioxidant c) is a tocopherol or a mixture of a tocopherol with a water-soluble antioxidant.

9. The formulation according to any one or more of the preceding claims, whereby the formulation comprises a reducing sugar, preferably in an amount from 1.0 to 5.0 weight-%, and a polyhydric alcohol, preferably in an amount from 0.1 to 5.0 weight-%, all amounts based on the total weight of a) to h).

10. The formulation according to claim 9, whereby the reducing sugar is glucose, fructose, galactose, high-fructose corn syrup, glucose syrup, dried glucose syrup, and any mixture thereof, and/or whereby the polyhydric alcohol is glycerol, sorbitol, xylitol, maltitol, erythritol, mannitol and any mixture thereof.

11. A container with a volume ranging from 450 l to 3000 l comprising a formulation according to any one or more of the preceding claims

12. The container according to claim 11, whereby the container has a volume ranging from 480 to 2000 l, preferably ranging from 500 to 1500 l, more preferably ranging from 500 to 1000 l, most preferably ranging from 600 to 800 l.

13. The container according to claim 11 and/or 12, whereby the container is a flexible intermediate bulk container.

14. A process for the manufacture of a formulation according to any one or more of the claims 1-10 comprising the following steps: A) Dissolving gelatin b), lignosulfonate c) and, if present, a water-soluble antioxidant c) in water to obtain a matrix; B) Heating the fat-soluble vitamin a), the fat-soluble antioxidant c) and, if present, the oil to obtain an active phase; C) Emulsifying the active phase obtained in step B) into the matrix obtained in step A) to obtain a dispersion; D) Spray-drying the dispersion obtained in step C) in presence of an anti-caking agent to obtain the formulation; whereby a reducing sugar and/or a polyhydric alcohol may optionally be added.

15. The process according to claim 14 further comprising an additional step: E) Thermal treating the formulation obtained in step D).

16. Use of the formulation according to any one or more of claims 1-10 as additive to feed or premixes.

17. Feed additive, premix or feed comprising the formulation according to any one or more of claims 1-10.