WO2001010988A1 - Huile de palme fractionnee et procede de production de celle-ci - Google Patents
Huile de palme fractionnee et procede de production de celle-ci Download PDFInfo
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- WO2001010988A1 WO2001010988A1 PCT/JP2000/004185 JP0004185W WO0110988A1 WO 2001010988 A1 WO2001010988 A1 WO 2001010988A1 JP 0004185 W JP0004185 W JP 0004185W WO 0110988 A1 WO0110988 A1 WO 0110988A1
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Classifications
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G1/00—Cocoa; Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/30—Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/32—Cocoa products, e.g. chocolate; Substitutes therefor characterised by the composition containing organic or inorganic compounds
- A23G1/36—Cocoa products, e.g. chocolate; Substitutes therefor characterised by the composition containing organic or inorganic compounds characterised by the fats used
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23D—EDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS, COOKING OILS
- A23D9/00—Other edible oils or fats, e.g. shortenings, cooking oils
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23D—EDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS, COOKING OILS
- A23D9/00—Other edible oils or fats, e.g. shortenings, cooking oils
- A23D9/02—Other edible oils or fats, e.g. shortenings, cooking oils characterised by the production or working-up
- A23D9/04—Working-up
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G1/00—Cocoa; Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/30—Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/32—Cocoa products, e.g. chocolate; Substitutes therefor characterised by the composition containing organic or inorganic compounds
- A23G1/36—Cocoa products, e.g. chocolate; Substitutes therefor characterised by the composition containing organic or inorganic compounds characterised by the fats used
- A23G1/38—Cocoa butter substitutes
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B7/00—Separation of mixtures of fats or fatty oils into their constituents, e.g. saturated oils from unsaturated oils
- C11B7/0008—Separation of mixtures of fats or fatty oils into their constituents, e.g. saturated oils from unsaturated oils by differences of solubilities, e.g. by extraction, by separation from a solution by means of anti-solvents
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B7/00—Separation of mixtures of fats or fatty oils into their constituents, e.g. saturated oils from unsaturated oils
- C11B7/0008—Separation of mixtures of fats or fatty oils into their constituents, e.g. saturated oils from unsaturated oils by differences of solubilities, e.g. by extraction, by separation from a solution by means of anti-solvents
- C11B7/0025—Separation of mixtures of fats or fatty oils into their constituents, e.g. saturated oils from unsaturated oils by differences of solubilities, e.g. by extraction, by separation from a solution by means of anti-solvents in solvents containing oxygen in their molecule
Definitions
- the present invention relates to a fractionated palm oil having sharp melting properties, and more particularly to a fractionated palm oil that can be used as a hard butter.
- a high melting point portion and a low melting point portion are removed from palm oil or palmolean to obtain a middle melting point portion of palm.
- the middle melting point of palm obtained in this way is used alone or mixed with shea butter, monkey fat, mango fat, etc., and used as a cocoa butter substitute fat for improving the physical properties of chocolate.
- the medium melting point of palm is mainly used for adjusting the hardness of chocolate and improving the sensation of mouth because it is mainly composed of oleoyl dipalmitin (P2 ⁇ ).
- Japanese Patent Application Laid-Open No. 53-80909 discloses a method of first removing palm oil from which high melting point is removed or not removed.
- a method for fractionating palm oil is disclosed in which at least 30% by weight of a low melting point portion is removed from a raw material fat and then the remainder is fractionated by a conventional method.
- Japanese Patent Application Laid-Open No. 60-217680 describes that the solid fat content is 70% or more at 20 ° C, 10% or more at 30 t, and 1% at 33 ° C.
- a cocoa butter primary substitute fat using palm middle oil which is 0 at 35 ° C.
- the fractionated palm oil obtained by this method is combined with mono-saturated di-unsaturated triglyceride (SUU) / tri-unsaturated triglyceride (UUU) / linoleyl di-saturated triglyceride (SLS), especially P 2 triglyceride. It is disclosed that the fat is adjusted by blending with fat having a large amount of fat to make confectionery fat.
- SUV mono-saturated di-unsaturated triglyceride
- UUU tri-unsaturated triglyceride
- SLS linoleyl di-saturated triglyceride
- the palm fractionated oil disclosed herein has a low melting point component SUU / UUU / SLS that imparts flexibility to the chocolate, it is blended with a SUU / UUU / S and S-rich fat, Hardness had to be adjusted by increasing the content of SUU / UUU / SLS.
- the middle melting point of the palm is mainly composed of P ⁇ ⁇ P
- the crystal tends to become coarse, and when blended in a large amount in chocolate, the gloss of the chocolate deteriorates with time and the bloom resistance is slightly inferior.
- the addition of an emulsifier that has an effect on the bloom resistance of ordinary hard butter to the conventional medium melting point of palm has no effect, and it has been extremely difficult to improve its bloom resistance.
- An object of the present invention is to provide chocolate with good heat resistance, snapping properties and sharp melting properties in the mouth without blending with other fats and oils, having sharp melting properties, It is an object of the present invention to provide a palm fractionated oil with a reduced increase in viscosity and a method for producing the same.
- Another object of the present invention is to provide a hard butter having good bloom resistance, and to significantly reduce the amount of hard butter in a chocolate box, which was difficult to design with conventional hard butter.
- the purpose is to provide chocolate that can be expanded and have better physical properties. Disclosure of the invention
- the present invention is characterized in that the content of linoleyl dipalmitin (P2) is 2 to 8% by weight, and the content of oleoyl dipalmitin (P20) is 70% by weight or more.
- the above objective has been achieved by providing fractionated palm oil.
- the present invention also relates to a method for producing a linoleyl dipalmitin (P 2 L) / trisaturated triglyceride (SSS) having a content of 0.5% by weight or less.
- Oleoyl dipalmitin (P20) A method for producing a fractionated palm oil, comprising removing a low-melting point fraction from a fractionated palm fraction having a weight ratio of 0.25 or less by solvent fractionation. Things.
- the present invention also provides a palm fractionated oil having a linoleyl dipalmitin (P 2 L) content of 2 to 8% by weight and an oleoyl dipalmitin (P 20) content of 70% by weight or more.
- a hard butter characterized by the following. Further, the present invention provides a hard butter containing an emulsifier in addition to the above hard butter.
- the present invention also provides a chocolate characterized by using the above hard butter.
- the fractionated palm oil of the present invention has a linoleyl dipalmitin (P 2 L) content of 2 to 8% by weight (hereinafter abbreviated as “%”), and a content of oleoyl dipalmitin (P 2 ⁇ ). Is more than 70%.
- the content of P2 is the total amount of PP and PLP, and is 2 to 8%, preferably 2 to 6%, and more preferably 2 to 4%. If the content of P 2 is less than 1%, the chick colate is too hard and lacks flexibility when used in chick collets, and if it is more than 8%, the heat resistance, snap properties, Poor speaking.
- the content of P20 is the total amount of PPO and POP, and is 70% or more, preferably 72% or more, and more preferably 74% or more. If the content of P20 is less than 70%, the snapping property when used in chocolate is poor, and a sharp mouthfeel cannot be obtained.
- 1 (3) -oleoyl dipalmitin (PP ⁇ ) weight% / 2-oleoyl dipalmitin (POP) weight% is 0.07 or less. More preferably, it is 0.055 or less, most preferably 0.04 or less. Chocolate if PPO / POP is greater than 0.07 When used in a batch, the snapping property tends to deteriorate, and it is difficult to obtain a sharp mouth.
- the fractionated palm oil of the present invention has a trisaturated triglyceride (sSS) content of 1.1.
- the content of S S S is more than 5%, it is not preferable because it has poor mouthfeel when used in chocolate and the workability during the tempering process is poor.
- the content of the diglyceride is more than 1%, the viscosity increases at the time of tempering, so that the workability is deteriorated and the mouth is deteriorated, which is not preferable.
- the fractionated palm oil of the present invention as described above has an iodine value of 38 to 50 (preferably 40 to 48) and a trisaturated triglyceride (SSS) content of 0.5% by weight or less. (Preferably 0.3% by weight or less), and linoleyl dipalmitin (P2L) / oleoyl dipalmitin (P20) [weight ratio] is 0.25 or less (preferably 0.20 or less). ) Can be obtained by removing the low melting point portion by solvent fractionation.
- SSS trisaturated triglyceride
- the iodine value is 38 to 50
- the content of trisaturated triglyceride (SSS) is 0.5% by weight or less
- linoleyl dipalmitin (P2L) / ole oil dipalmitin (P2 ⁇ ) A palm fraction having a [weight ratio] of 0.25 or less can be obtained by the following methods (1) to (4).
- a solution obtained by completely melting a medium melting point portion of a palm having an iodine value of 40 to 50 is cooled to 24 to 27 ° C, preferably 25 to 26 ° C, and a crystal is deposited. Is removed.
- the obtained fractionated raw material miscella is cooled, but when acetone is used as a solvent, it is 15 to 5 ° (preferably, 2 to 2 ° C, and when hexane is used, it is 15 to 15 °). It is cooled to 0 ° C, preferably to 110 ° C to 15 ° C, to obtain a crystal part. It will be easier.
- the obtained olein fraction is completely dissolved, and cooled to 10 to 20 ° C, preferably 12 to 18 ° C, to precipitate crystals to obtain a crystalline portion.
- a seed serving as a nucleus of the crystal pamstearin, permolein, or another solid fat previously cooled and solidified
- the palm oil is completely melted and cooled to 16 to 24 ° C, preferably 16 to 20 ° C to precipitate crystals, remove the crystal part, and have an iodine value of 56 to 59, Olein fraction with SSS content of 0.3% or less is obtained.
- the obtained fractionated raw material miscella is cooled, but when acetone is used as a solvent, it is 15 to 5 ° (preferably, 12 to 2 t, and when hexane is used, it is 15 to 5 °). It is cooled to 0 ° C, preferably to 110--5 ° C, to obtain a crystal part. It will be easier.
- the iodine value obtained by the above method (1) to (3) is 38 to 50
- the content of trisaturated triglyceride (SSS) is 0.5% by weight or less
- SSS trisaturated triglyceride
- P 2 L linoleic dipalmitin
- P 2 ⁇ Oley oil dipalmitin
- the removal of the low melting point portion by the solvent separation is performed as follows.
- the obtained fractionated raw material miscella is cooled.
- the temperature is 5 to 15 ° C., preferably 7 to 13 ° C.
- hexane when used, 10 to 10 ° C. Cool to -5 ° C, preferably 15 ° C to 0 ° C to precipitate crystals to obtain a crystal part.
- a polar solvent such as acetone for a more efficient removal of diglyceride than a nonpolar solvent such as hexane.
- crystallization is facilitated by adding a seed that becomes a crystal nucleus (a material obtained by preliminarily cooling and crystallizing the fractionated raw material such as miscella).
- the palm of the present invention having a linoleyl dipalmitin (P 2 L) content of 2 to 8% by weight and an oleoyl dipalmitin (P 20) content of 70% by weight or more.
- P 2 L linoleyl dipalmitin
- P 20 oleoyl dipalmitin
- the obtained palm fractionated oil of the present invention can be used as a hard flap.
- the fractionated palm oil of the present invention can be used as hard butter in chocolate.
- fractionated palm oil of the present invention is used for confectionery fats and oils suitable for kneading fats, spray fats, cream fats and the like in addition to chocolate.
- the hard butter of the present invention and chocolate using the same will be described in detail.
- the content of linoleyl dipalmitoyl Chin (P 2 L) is 2 to 8 weight 0/6
- the content of O Les oil dipalmitoyl Chin (P 2 0) is a 7 0 wt% or more It consists of palm fractionated oil.
- the hard butter of the present invention may be composed of only the above-mentioned fractionated palm oil, but may include cocoa butter, monkey fat, shea butter, lipe butter, mango kernel oil, cocoum butter, these fractionated oils, and transesterified oils. May be mixed with fractionated palm oil.
- the amount of the fractionated palm oil, in the hard butter of the present invention preferably 1 by weight 0/6 or more, more preferably 3 wt% or more.
- an emulsifier to the hard butter of the present invention.
- Use of an emulsifier improves bloom resistance.
- the emulsifier at this time is not limited as long as it can be used for food.
- a polyglycerin fatty acid ester or a sucrose fatty acid ester is used.
- Emulsifying Qi is in Hadobata aspect of the present invention, preferably 0. 0 5 to 1 5% by weight, preferably in further 0. 1 ⁇ i 2%, most preferably from 0.2 to 8 weight 0 6 is contained. If the amount of emulsifier is less than 0.05% by weight, the bloom suppressing effect is weak, and the amount exceeds 15% by weight. The taste tends to be impaired and the mouthfeel becomes worse.
- polyglycerol fatty acid ester those having a degree of polymerization of glycerin of 4 to 10, preferably 6 to 8, and esterified with an average of 4 mol or more, preferably 6 mol or more of fatty acids are desirable.
- Fatty acids constituting the polyglycerol fatty acid ester include fatty acids having up to 24 carbon atoms, preferably saturated fatty acids having 16 to 22 carbon atoms.
- sucrose fatty acid ester examples include those having a saturated fatty acid having an HLB of 1 or less and having up to 24 carbon atoms in the constituent fatty acids, and preferably having 16 to 22 carbon atoms.
- sorbitan fatty acid ester examples include those in which the HLB is 3 or less and the constituent fatty acid is a fatty acid having up to 2 carbon atoms, preferably a saturated fatty acid having 16 to 22 carbon atoms.
- the hard butter of the present invention may contain an emulsifier other than the above-mentioned emulsifiers, cacao content, sugar, protein, dairy products, carbohydrates, vitamins, seasonings, spices, moisture, etc., which are usually contained in chocolate. You may.
- the hard butter of the present invention comprising the above-mentioned palm fractionated oil is used for chocolate.
- the mixing amount of the hard butter is preferably 1 to 60 parts by weight, more preferably! ⁇ 50 parts by weight.
- the chocolate of the present invention is obtained by using this hard butter, and has good heat resistance, snapping properties, and melting characteristics that are sharp in the mouth.
- the present invention will be described in more detail with reference to examples, but the present invention is not limited to these examples.
- the palmollen (cloud point 10 ° C, iodine value 56.3) was heated at 60 ° C for 1 hour to completely melt. This was cooled to 20 ° C in 4 hours with gentle stirring, and the palm oil crystals obtained by cooling to 30 ° C were used as seeds, and Was added to the mixture, and the mixture was further kept at 20 ° C. for 2 hours. Then, the filtrate was separated into 95% by weight of the filtrate portion and 5% by weight of the crystal portion to obtain a filtrate portion having an iodine value of 56.7 and an SSS content of 0.1% by weight.
- the second separation was performed in the following manner. 300 parts by weight of acetone was added to 100 parts by weight of the filtrate to the filtrate obtained in the first fractionation, to give a fractionated raw material mixer. This was heated at 45 ° C for 30 minutes to completely dissolve it. And. The mixture was cooled to 10 ° C. over 2 hours with gentle stirring, and 1% by weight of a seed was added to the separated raw material miscella. As a seed, a crystal obtained by cooling the fractionated raw material Misera to 120 ° C was used. Further, the mixture was cooled to 0 ° C over 2 hours with gentle stirring, kept at 0 ° C for 1 hour, filtered, and separated into 60% by weight of olein fraction and 40% by weight of stearin fraction. The obtained stealine fraction (palm fraction) has an iodine value of 42.1, an SSS content of 0.1% by weight, and a P 2 / P 2 [weight ratio] of 0.1. It was nine.
- the third separation was performed in the following manner. To 100 parts by weight of the stealine fraction obtained in the second fractionation, 300 parts by weight of acetone was added to obtain a fractionating raw material miscella. This was heated at 50 ° C for 30 minutes to completely dissolve, then cooled to 18 ° C in 2 hours with gentle stirring, and used for the second separation. The same seed was added at 1% by weight to the miscellaneous material Misera. Then, the mixture was cooled to 10 ° C. in 2 hours with gentle stirring, kept for 1 hour, filtered, and separated into an olein fraction of 40% by weight and a stearin fraction of 60% by weight.
- Table 1 shows the triglyceride composition and solid fat content (SFC) of the obtained stearin fraction (palm fractionated oil).
- the palm oil was heated at 60 ° C for 1 hour to completely dissolve it. This was cooled to 18 ° C. in 3 hours with gentle stirring and maintained for 6 hours. Then, it was separated into a filtrate portion of 75% by weight and a crystal portion of 25% by weight. The obtained filtrate portion had an iodine value of 57.0 and SSS of 0.1% by weight.
- the second separation was performed in the following manner. Filter obtained from the first separation To the liquid portion, 300 parts by weight of acetone was added with respect to 100 parts by weight of the filtrate to obtain a miscellaneous raw material misera. This was heated at 45 ° C for 30 minutes to completely dissolve it. Then, the mixture was cooled to 10 ° C. in 1 hour with gentle stirring, and a 1% by weight seed was added to the separated raw material miscella. As a seed, a crystal obtained by cooling the fractionated raw material Misera to 120 ° C was used. Furthermore, the mixture was cooled to 0 ° C in 2 hours while continuing to stir slowly, and kept at 0 ° C for 1 hour. did. The obtained stearin fraction (palm fraction) has an iodine value of 42.0, an SSS content of 0.1% by weight, and a P 2 L / P 20 [weight ratio] of 0.2. It was 0.
- the third separation was performed in the following manner. To 100 parts by weight of the stearin fraction obtained in the second fractionation, 300 parts by weight of acetone was added to obtain a fractionating raw material miscella. This was heated at 50 ° C for 30 minutes to completely dissolve, then cooled to ⁇ 8 ° C in 2 hours with gentle stirring, and used for the second separation. The same shade as in Example 1 was added at 1% by weight to the miscellaneous raw material misera. Then, the mixture was cooled to 10 ° C. over 1 hour while stirring slowly, and after holding for 1 hour, filtered, and separated into an olein fraction of 40% by weight and a stearin fraction of 60% by weight.
- Table shows the tridaliceride composition and SFC of the obtained stearin fraction (palm fractionated oil).
- the palm middle melting point (iodine value 47.1) was heated at 60 ° C. for 1 hour to completely dissolve it. This was cooled to 25 ° C. in 3 hours with gentle stirring and maintained for 13 hours. Then, the filtrate was separated into 93% by weight of the filtrate portion and 7% by weight of the crystal portion.
- the obtained filtrate portion (palm fraction) has an iodine value of 48.2, a content of 5.55 of 0.1 weight 0/6 , and a P 2 L / P 20 [weight ratio] of 0. 22
- the second separation was performed in the following manner. 400 parts by weight of acetone was added to 100 parts by weight of the filtrate obtained in the first fractionation to obtain a miscellaneous raw material, miscella. Heat this at 45 ° C for 30 minutes to completely dissolve it, and then The mixture was cooled to 15 ° C. in one hour, and 0.2% by weight of a shield was added to the fractionated raw material misera. As a seed, a crystal obtained by cooling the fractionated raw material Misera at 120 ° C. was used. Then, the mixture was cooled down to 8 ° C in 1 hour with gentle stirring, filtered for 1 hour, and separated into 55% by weight of olein fraction and 45% by weight of stealine fraction. Table 1 shows the triglyceride composition and SFC of the stearin fraction (palm fractionated oil).
- the first and second separations were performed in the same manner as in Example 1.
- fractionation was carried out in the same manner as in Example 1 except that the final cooling temperature was changed from 10 ° C in Example 1 to 0 ° C. The fraction was separated into 80% by weight.
- Table 1 shows the triglyceride composition and SFC of the obtained stearin fraction (palm fractionated oil).
- Example 1 the first separation was performed as follows. 300 parts by weight of acetone was added to 100 parts by weight of palm olein (cloud point: 10 °, iodine value: 56.3) to obtain a miscellaneous raw material miscella. This was heated at 45 ° C for 30 minutes to completely dissolve, then cooled to 15 ° C in 2 hours with gentle stirring, and 1% by weight of seed was added to the separated miscella. Was added. As a seed, a crystal obtained by cooling the fractionated raw material Misera to 120 ° C was used. Then, the mixture was cooled to 0 in 2 hours while continuing to stir slowly, filtered at 1 ° C.
- the obtained stearin fraction (palm fraction) has an iodine value of 44.7, an SSS content of 1.1% by weight, and a P 2 L / P 20 [weight ratio] of 0.2.
- the obtained stearin fraction has an iodine value of 44.7, an SSS content of 1.1% by weight, and a P 2 L / P 20 [weight ratio] of 0.2.
- the second separation was performed in the following manner. 300 parts by weight of acetone was added to 100 parts by weight of the crystals obtained in the first fractionation, to give a miscellaneous raw material miscella. This After heating at 50 ° C for 30 minutes to completely dissolve, the mixture was cooled to 15 ° C in 2 hours with gentle stirring, and 1% by weight of seed was added to the separated raw material miscella. . As a seed, a crystal obtained by cooling the fractionated raw material misera to 120 ° C. was used. Then, cooled to 0 ° C 2 hours with continued slowly retriever stirring, filtered after 1 hour hold was fractionated into Orein fraction 1 0 weight 0 6 and stearin fraction 8 0 wt%.
- Table 1 shows the triglyceride composition and SFC of the obtained stearin fraction (palm fractionated oil).
- the first separation was performed in the same manner as in Comparative Example 2.
- the second separation was performed in the same manner as in Comparative Example 2 except that the final cooling temperature was changed from 0 ° C to 10 ° C in Comparative Example 2.
- perform fractionation in the same manner Table 1 Bok Riguriseri de composition and SFC of Orein fraction 2 5 wt% and stearin fraction 7 5 wt 0/6 and stearin fraction obtained was fractionated into (fractionated palm oil) Shown in
- SFC solid content
- the PPO / PO P ratio was determined by measuring the fat ⁇ ffiJ ⁇ at the 2-position of the P20 fraction after obtaining the P20 fraction by preparative HPLC, and 10% of the ⁇ prepared HPLC C fla3 ⁇ 4 ⁇
- chocolate was produced with the composition shown in Table 2.
- Table 3 shows the chocolate production test and the evaluation of the obtained chocolate pellets.
- Example fractionated palm oil 9 9 weight obtained in 2 0/0 and sorbitan fatty acid esters (Seo Rubitan Bok tristearate, H and B 2. 5) use the hard butter consisting of 1% by weight, shown in Table 2 A chocolate was produced with the formula. Table 3 shows the chocolate production test and the evaluation of the obtained thiocholate.
- Chocolate was produced with the composition shown in Table 2 using a hard butter consisting of 99% by weight of the palm fractionated oil obtained in Comparative Example 2 and 1% by weight of a sucrose fatty acid ester (sucrose stearate, HLB 1 or less). .
- Table 3 shows the chocolate production test and the evaluation of the obtained chocolate.
- the chocolate thus obtained was aged at 20 ° C. for one week, and each evaluation shown in Table 3 was performed. Table 3 shows the results. Note that 'snap property' is an evaluation of the hardness of the protruding piece (whether it makes a sharp sound and breaks), and 'sharp melt property' is an evaluation that includes the sharpness of the chocolate in the latter half of the chocolate. However, these evaluations are based on the evaluation when 10 people tasted. In the bloom resistance test, chocolate was placed at 20 ° C for 12 hours and then placed at 28 ° C for 12 hours. Below, the change over time of the chocolate surface was observed, and the number of cycles required until bloom was observed on the surface was indicated by ⁇ .
- the balm fractionated oil of the present invention has a linoleyl dipalmitin (P 2) content of 2 to 2.
- oleoyl dipalmitin P20
- P20 oleoyl dipalmitin
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Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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EP00939166A EP1120455A4 (en) | 1999-08-09 | 2000-06-26 | FRACTIONATED PALMOEL AND METHOD FOR PRODUCING THE SAME |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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JP11/225281 | 1999-08-09 | ||
JP11225281A JP2000336389A (ja) | 1998-09-22 | 1999-08-09 | パーム分別油及びその製造方法 |
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WO2001010988A1 true WO2001010988A1 (fr) | 2001-02-15 |
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PCT/JP2000/004185 WO2001010988A1 (fr) | 1999-08-09 | 2000-06-26 | Huile de palme fractionnee et procede de production de celle-ci |
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ID (1) | ID27808A (ja) |
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KR101486303B1 (ko) * | 2007-12-21 | 2015-01-26 | 로더스 크로클란 비.브이. | 팜 오일 생성물을 제조하는 방법 |
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BRPI1009677B8 (pt) | 2009-06-12 | 2018-11-21 | Mars Inc | gelificação de polímero de óleos |
CN101912034B (zh) * | 2010-08-28 | 2012-07-11 | 青岛农业大学 | 一种过瘤胃物质的保护脂肪 |
GB2485421B (en) | 2010-11-15 | 2016-05-25 | Mars Inc | Dough products exhibiting reduced oil migration |
WO2014052312A1 (en) | 2012-09-28 | 2014-04-03 | Mars, Incorporated | Heat resistant chocolate |
CA2906803C (en) * | 2013-03-15 | 2018-05-01 | The Hershey Company | Method of making a heat stable chocolate confectionery product |
JP2018130071A (ja) * | 2017-02-16 | 2018-08-23 | 不二製油株式会社 | チョコレート類及びその製造方法 |
WO2024178287A2 (en) * | 2023-02-23 | 2024-08-29 | Cargill, Incorporated | Process for producing a palm oil fraction |
WO2024178286A1 (en) * | 2023-02-23 | 2024-08-29 | Cargill, Incorporated | Process for producing a palm oil fraction using seeds |
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US3492130A (en) * | 1966-11-21 | 1970-01-27 | Scm Corp | Hard butter compositions and method of production |
GB1510082A (en) * | 1975-04-14 | 1978-05-10 | Asahi Denka Kogyo Kk | Process for the fractionation of glyceride oils or fats and producing a hard butter |
JPS55114261A (en) * | 1979-02-24 | 1980-09-03 | Fuji Oil Co Ltd | Chocolate for flozen food |
EP0130487A2 (en) * | 1983-06-29 | 1985-01-09 | Asahi Denka Kogyo Kabushiki Kaisha | Cacao butter substitutes and chocolates containing the same |
EP0426155A2 (en) * | 1989-10-31 | 1991-05-08 | Kao Corporation | Hard butter composition |
JPH06116582A (ja) * | 1992-10-06 | 1994-04-26 | Kanegafuchi Chem Ind Co Ltd | 油脂の洗浄方法 |
JPH07303448A (ja) * | 1994-05-11 | 1995-11-21 | Kao Corp | ハードバター組成物及びチョコレート様食品 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03292856A (ja) * | 1990-04-11 | 1991-12-24 | Asahi Denka Kogyo Kk | 油脂組成物 |
EP0545463B1 (en) * | 1991-11-26 | 1995-04-26 | Unilever N.V. | Non-tempering confectionery fat |
-
2000
- 2000-06-26 ID IDW20010684A patent/ID27808A/id unknown
- 2000-06-26 EP EP00939166A patent/EP1120455A4/en not_active Withdrawn
- 2000-06-26 WO PCT/JP2000/004185 patent/WO2001010988A1/ja not_active Application Discontinuation
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3492130A (en) * | 1966-11-21 | 1970-01-27 | Scm Corp | Hard butter compositions and method of production |
GB1510082A (en) * | 1975-04-14 | 1978-05-10 | Asahi Denka Kogyo Kk | Process for the fractionation of glyceride oils or fats and producing a hard butter |
JPS55114261A (en) * | 1979-02-24 | 1980-09-03 | Fuji Oil Co Ltd | Chocolate for flozen food |
EP0130487A2 (en) * | 1983-06-29 | 1985-01-09 | Asahi Denka Kogyo Kabushiki Kaisha | Cacao butter substitutes and chocolates containing the same |
EP0426155A2 (en) * | 1989-10-31 | 1991-05-08 | Kao Corporation | Hard butter composition |
JPH06116582A (ja) * | 1992-10-06 | 1994-04-26 | Kanegafuchi Chem Ind Co Ltd | 油脂の洗浄方法 |
JPH07303448A (ja) * | 1994-05-11 | 1995-11-21 | Kao Corp | ハードバター組成物及びチョコレート様食品 |
Non-Patent Citations (1)
Title |
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See also references of EP1120455A4 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101486303B1 (ko) * | 2007-12-21 | 2015-01-26 | 로더스 크로클란 비.브이. | 팜 오일 생성물을 제조하는 방법 |
Also Published As
Publication number | Publication date |
---|---|
ID27808A (id) | 2001-04-26 |
EP1120455A1 (en) | 2001-08-01 |
EP1120455A4 (en) | 2003-04-16 |
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