JP5960431B2 - Fat and oil creaming improver and oil and fat composition containing the same - Google Patents
Fat and oil creaming improver and oil and fat composition containing the same Download PDFInfo
- Publication number
- JP5960431B2 JP5960431B2 JP2011287879A JP2011287879A JP5960431B2 JP 5960431 B2 JP5960431 B2 JP 5960431B2 JP 2011287879 A JP2011287879 A JP 2011287879A JP 2011287879 A JP2011287879 A JP 2011287879A JP 5960431 B2 JP5960431 B2 JP 5960431B2
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- Prior art keywords
- oil
- creaming
- fatty acid
- fat
- acid
- Prior art date
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- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 235000020183 skimmed milk Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229940080237 sodium caseinate Drugs 0.000 description 1
- 235000019830 sodium polyphosphate Nutrition 0.000 description 1
- 229950004959 sorbitan oleate Drugs 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 125000005472 straight-chain saturated fatty acid group Chemical group 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 235000020238 sunflower seed Nutrition 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 235000019149 tocopherols Nutrition 0.000 description 1
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- 229940045997 vitamin a Drugs 0.000 description 1
- 235000008939 whole milk Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Edible Oils And Fats (AREA)
- Fats And Perfumes (AREA)
Description
本発明は、油脂のクリーミング性向上剤およびそれを含有する油脂組成物に関する。 TECHNICAL FIELD The present invention relates to an oil / fat creaming improver and an oil / fat composition containing the same.
パン・菓子類の多くは、シュガーバッター法と呼ばれる方法で製造される。この方法は、ショートニングやマーガリンを蔗糖と撹拌して空気を抱き込ませ、次いで、卵、牛乳、糖液等を抱き込ませ、最後に小麦粉を軽く合わせて焼成させるというものである。このため、パン・菓子類の製造に用いるショートニングやマーガリン等の油脂組成物は、空気を抱き込む性質(クリーミング性)および卵、牛乳、糖液等を抱き込む性質(吸水性)が求められる。また、バタークリームやサンドクリーム等の製造においても、予め油脂を撹拌して空気を抱き込ませた後、卵等を抱き込ませるため、油脂にクリーミング性および吸水性を付与することが求められる。 Many of bread and confectionery are manufactured by a method called a sugar batter method. In this method, shortening or margarine is stirred with sucrose to embed air, then eggs, milk, sugar solution, etc. are embraced, and finally the flour is lightly combined and baked. For this reason, oil and fat compositions such as shortening and margarine used for the manufacture of bread and confectionery are required to have a property of embracing air (creaming properties) and a property of embracing eggs, milk, sugar solution and the like (water absorption). Also, in the production of butter cream, sand cream, etc., it is required to impart creaming properties and water absorption to the oil and fat in order to entrap the oil and fat before embedding the air and then the egg and the like.
油脂にクリーミング性や吸水性を付与する方法としては、例えば、1種又は2種以上のジグリセライドを含有する油脂組成物であって、上昇融点が20℃未満のジグリセライドを基準にして10〜99重量%含有することを特徴とする高起泡性油脂組成物(特許文献1)、HLBが3以下であって、構成脂肪酸が、炭素数12〜22の飽和脂肪酸20〜80重量%及び炭素数16〜22の不飽和脂肪酸80〜20重量%からなる多価アルコール脂肪酸エステルを有効成分とする油脂の結晶成長抑制剤(特許文献2)、成分(A)パーム油を50重量%以上と、成分(B)ポリグリセリン脂肪酸エステルを0.05〜5重量%とを含有する油脂組成物であって、該成分(B)のエステル化率が50%以上、該成分(B)の構成脂肪酸の80重量%以上がオレイン酸とパルミチン酸からなり、オレイン酸とパルミチン酸とのモル比が90:10〜10:90であることを特徴とする油脂組成物(特許文献3)、飽和脂肪酸結合型ソルビタン脂肪酸エステルを有効成分とするクリーミング性向上剤(特許文献4)などが提案されている。 As a method of imparting creaming properties and water absorption to fats and oils, for example, an oil or fat composition containing one or more diglycerides and having an ascending melting point of less than 20 ° C. is 10 to 99 wt. % High foaming oil and fat composition (Patent Document 1), HLB is 3 or less, and the constituent fatty acid is 20 to 80% by weight of saturated fatty acid having 12 to 22 carbon atoms and 16 carbon atoms. A crystal growth inhibitor of fats and oils comprising a polyhydric alcohol fatty acid ester consisting of 80 to 20% by weight of an unsaturated fatty acid of ˜22 as an active ingredient (Patent Document 2), 50% by weight or more of component (A) palm oil, B) An oil and fat composition containing 0.05 to 5% by weight of a polyglycerol fatty acid ester, wherein the component (B) has an esterification rate of 50% or more, and 80% by weight of the constituent fatty acid of the component (B) The above is composed of oleic acid and palmitic acid, and the molar ratio of oleic acid to palmitic acid is 90:10 to 10:90, (Patent Document 3), saturated fatty acid-binding sorbitan fatty acid ester A creaming property improver (Patent Document 4) and the like, in which an active ingredient is used as an active ingredient, has been proposed.
上記方法はいずれも、油脂が空気を抱き込む量を示す指標である「クリーミング価」や油脂が水・卵等を抱き込む量を示す指標である「吸水量」を高めるという観点から提案されたものである。しかし、パン・菓子類等をより効率良く生産するためには、クリーミング価や吸水量を高めるだけでなく、クリーミングに要する時間や油脂組成物に卵等を添加して均一化するのに要する時間をより短縮する方法が求められている。 All of the above methods were proposed from the viewpoint of increasing the “creaming value” that is an index indicating the amount of fats and oils that entrap air, and the “water absorption” that is an index that indicates the amount of oils and fats that embrace water, eggs, and the like. Is. However, in order to produce bread, confectionery, etc. more efficiently, not only the creaming value and water absorption are increased, but also the time required for creaming and the time required for homogenization by adding eggs etc. to the fat composition. There is a need for a method for shortening the above.
本発明は、クリーミング速度および吸水速度をさらに向上できる油脂のクリーミング性向上剤並びに該クリーミング性向上剤を含有する油脂組成物を提供することを課題とする。 An object of the present invention is to provide an oil and fat creaming property improver capable of further improving the creaming rate and the water absorption rate, and an oil and fat composition containing the creaming property improving agent.
本発明者は、上記課題を解決するため、鋭意検討した結果、特定の乳化剤を添加した油脂組成物は、該油脂組成物を使用してパン・菓子類等を生産する際のクリーミング速度および吸水速度がさらに向上したものであることを見出し、この知見に基づいて本発明をなすに至った。 As a result of intensive studies to solve the above-mentioned problems, the present inventors have found that an oil and fat composition added with a specific emulsifier has a creaming rate and water absorption when producing bread and confectionery using the oil and fat composition. It was found that the speed was further improved, and the present invention was made based on this finding.
すなわち、本発明は、
(1)グリセリン有機酸脂肪酸エステルおよび/またはソルビタン不飽和脂肪酸エステルを有効成分とすることを特徴とする油脂のクリーミング性向上剤、
(2)前記(1)に記載のクリーミング性向上剤を含有することを特徴とする油脂組成物、からなっている。
That is, the present invention
(1) A fat and oil creaming improver characterized by comprising a glycerin organic acid fatty acid ester and / or a sorbitan unsaturated fatty acid ester as an active ingredient,
(2) It comprises an oil or fat composition characterized by containing the creaming improver as described in (1) above.
本発明のクリーミング性向上剤は、油脂組成物のクリーミング速度、吸水速度および吸卵速度を十分に向上することができる。
本発明の油脂組成物は、クリーミング速度、吸水速度および吸卵速度が十分に向上したものであるため、パン・菓子類の生産効率を高めるために用いることができる。
The creaming property improver of the present invention can sufficiently improve the creaming rate, water absorption rate and egg absorption rate of the oil and fat composition.
The oil and fat composition of the present invention has sufficiently improved creaming speed, water absorption speed and egg absorption speed, and can be used to increase the production efficiency of bread and confectionery.
本発明に用いられるグリセリン有機酸脂肪酸エステルとしては、例えば、グリセリン酢酸脂肪酸エステル(食品添加物)、グリセリン乳酸脂肪酸エステル(食品添加物)、グリセリンクエン酸脂肪酸エステル(食品添加物)、グリセリンコハク酸脂肪酸エステル(食品添加物)などが挙げられ、油脂組成物に吸水速度を十分に付与する観点から、グリセリンクエン酸脂肪酸エステルまたはグリセリンコハク酸脂肪酸エステルが好ましく用いられる。なお、グリセリンクエン酸脂肪酸エステルまたはグリセリンコハク酸脂肪酸エステルを用いると油脂組成物の吸水速度が十分に向上するため、これらは油脂の吸水性向上剤として使用することもできる。グリセリン有機酸脂肪酸エステルを構成する脂肪酸としては、食用可能な動植物油脂を起源とする脂肪酸であれば特に制限はなく、例えば炭素数6〜24の直鎖の飽和脂肪酸(例えば、カプロン酸、カプリル酸、カプリン酸、ラウリン酸、ミリスチン酸、パルミチン酸、ステアリン酸、アラキジン酸、ベヘン酸、リグノセリン酸など)および不飽和脂肪酸(例えば、パルミトオレイン酸、オレイン酸、エライジン酸、リノール酸、γ−リノレン酸、α−リノレン酸、アラキドン酸、リシノール酸、縮合リシノール酸など)が挙げられ、好ましくは炭素数16〜18の飽和または不飽和脂肪酸である。 Examples of the glycerin organic acid fatty acid ester used in the present invention include glycerin acetic acid fatty acid ester (food additive), glycerin lactic acid fatty acid ester (food additive), glycerine citrate fatty acid ester (food additive), glycerin succinic acid fatty acid. Examples include esters (food additives), and glycerin citrate fatty acid esters or glycerin succinic acid fatty acid esters are preferably used from the viewpoint of sufficiently imparting a water absorption rate to the oil and fat composition. In addition, since the water absorption rate of fats and oils composition will fully improve when glycerine citrate fatty acid ester or glycerin succinic acid fatty acid ester is used, these can also be used as a water absorption improvement agent of fats and oils. The fatty acid constituting the glycerin organic acid fatty acid ester is not particularly limited as long as it is derived from edible animal and vegetable oils and fats. For example, straight-chain saturated fatty acids having 6 to 24 carbon atoms (for example, caproic acid and caprylic acid). , Capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, arachidic acid, behenic acid, lignoceric acid, etc.) and unsaturated fatty acids (eg palmitooleic acid, oleic acid, elaidic acid, linoleic acid, γ-linolenic acid) Acid, α-linolenic acid, arachidonic acid, ricinoleic acid, condensed ricinoleic acid, etc.), and preferably a saturated or unsaturated fatty acid having 16 to 18 carbon atoms.
なお、グリセリン有機酸脂肪酸エステルとしては、ポエムK−30(商品名;グリセリンクエン酸脂肪酸エステル;理研ビタミン社製)、ポエムK−37V(商品名;グリセリンクエン酸脂肪酸エステル;理研ビタミン社製)、ポエムB−30(商品名;グリセリンコハク酸脂肪酸エステル;理研ビタミン社製)などが商業的に製造および販売されており、本発明のクリーミング性向上剤にはこれらを用いることができる。 In addition, as glycerol organic acid fatty acid ester, Poem K-30 (trade name; glycerine citrate fatty acid ester; manufactured by Riken Vitamin Co., Ltd.), Poem K-37V (trade name; glycerin citrate fatty acid ester; manufactured by Riken Vitamin Co., Ltd.), Poem B-30 (trade name; glycerin succinic acid fatty acid ester; manufactured by Riken Vitamin Co., Ltd.) and the like are commercially produced and sold, and these can be used as the creaming improver of the present invention.
本発明において用いられるソルビタン不飽和脂肪酸エステルは、酸またはアルカリ触媒存在下、ソルビトールまたはソルビトール分子内縮合物と不飽和脂肪酸との直接エステル化反応により得ることができる。 The sorbitan unsaturated fatty acid ester used in the present invention can be obtained by direct esterification reaction of sorbitol or sorbitol intramolecular condensate with an unsaturated fatty acid in the presence of an acid or an alkali catalyst.
上記エステル化反応で用いられるソルビトールとしては、例えば、D−ソルビトールを約50.0〜70.0質量%含有するD−ソルビトール液或いは白色粉末または粒状のD−ソルビトールが挙げられる。 Examples of the sorbitol used in the esterification reaction include D-sorbitol liquid containing about 50.0 to 70.0% by mass of D-sorbitol, white powder, or granular D-sorbitol.
上記エステル化反応で用いられるソルビトール分子内縮合物は、ソルビトールの分子内脱水で得られる化合物であり、例えば1,5−ソルビタン、1,4−ソルビタン、2,5−ソルビタン、3,6−ソルビタン、1,4,3,6−ソルバイドなどが挙げられる。これらソルビトール分子内縮合物は、1種類でまたは2種類以上を組み合わせて用いることができる。また本発明で用いられるソルビトール分子内縮合物中には、上記化合物以外に、未反応のソルビトールが含まれていても良い。 The sorbitol intramolecular condensate used in the esterification reaction is a compound obtained by intramolecular dehydration of sorbitol. For example, 1,5-sorbitan, 1,4-sorbitan, 2,5-sorbitan, 3,6-sorbitan 1,4,3,6-sorbide and the like. These sorbitol intramolecular condensates can be used alone or in combination of two or more. The sorbitol intramolecular condensate used in the present invention may contain unreacted sorbitol in addition to the above compounds.
ソルビトールの分子内脱水反応は、酸触媒(例えば濃硫酸、p−トルエンスルホン酸など)の存在下に、ソルビトールを約110〜150℃、好ましくは約120℃で加熱し、減圧下、例えば約1.3kPaで、発生する水を除去することにより行われるのが好ましい。反応の終点は脱水縮合物の水酸基価を測定することにより決定される。反応終了後、脱水縮合物に例えば水酸化ナトリウム水溶液を加えて酸触媒を中和し、更に、例えば珪藻土などのろ過助剤を加えてろ過するのが好ましい。 The intramolecular dehydration reaction of sorbitol is carried out by heating sorbitol at about 110 to 150 ° C., preferably about 120 ° C. in the presence of an acid catalyst (for example, concentrated sulfuric acid, p-toluenesulfonic acid, etc.), for example, about 1 It is preferably carried out by removing the generated water at .3 kPa. The end point of the reaction is determined by measuring the hydroxyl value of the dehydrated condensate. After completion of the reaction, it is preferable to add a sodium hydroxide aqueous solution to the dehydrated condensate to neutralize the acid catalyst, and further filter with a filter aid such as diatomaceous earth.
上記エステル化反応で用いられる不飽和脂肪酸としては、食用可能な動植物油脂を起源とし、炭素原子間の結合に二重結合を含む脂肪酸であれば特に制限はなく、例えばパルミトオレイン酸、オレイン酸、エライジン酸、リノール酸、γ−リノレン酸、α−リノレン酸、アラキドン酸、リシノール酸、縮合リシノール酸などが挙げられる。これら脂肪酸は一種類で用いても良いし、二種類以上を任意に組み合わせて用いても良い。油脂組成物にクリーミング速度を十分に付与する観点から、好ましくは、オレイン酸である。 The unsaturated fatty acid used in the esterification reaction is not particularly limited as long as it is derived from edible animal and vegetable fats and oils and contains a double bond between carbon atoms. For example, palmitooleic acid, oleic acid Elaidic acid, linoleic acid, γ-linolenic acid, α-linolenic acid, arachidonic acid, ricinoleic acid, condensed ricinoleic acid and the like. These fatty acids may be used alone or in any combination of two or more. From the viewpoint of sufficiently imparting a creaming speed to the oil and fat composition, oleic acid is preferable.
上記エステル化反応において、ソルビトールまたはソルビトール分子内縮合物に対する脂肪酸の仕込み量は、ソルビトールまたはソルビトール分子内縮合物1モルに対しておおむね1〜2モル程度であるのが好ましい。 In the esterification reaction, the amount of fatty acid charged to sorbitol or sorbitol intramolecular condensate is preferably about 1 to 2 moles per mole of sorbitol or sorbitol intramolecular condensate.
ソルビトールまたはソルビトール分子内縮合物と脂肪酸とのエステル化反応は無触媒で行って良く、または酸触媒あるいはアルカリ触媒を用いて行っても良いが、アルカリ触媒の存在下で行われるのが好ましい。アルカリ触媒としては、例えば水酸化カリウム、水酸化ナトリウム、炭酸カリウム、炭酸ナトリウムなどが挙げられる。アルカリ触媒の使用量は、全仕込み量(乾燥物換算)の約0.01〜1.0質量%、好ましくは約0.05〜0.5質量%である。 The esterification reaction between sorbitol or sorbitol intramolecular condensate and a fatty acid may be carried out without a catalyst, or may be carried out using an acid catalyst or an alkali catalyst, but is preferably carried out in the presence of an alkali catalyst. Examples of the alkali catalyst include potassium hydroxide, sodium hydroxide, potassium carbonate, sodium carbonate and the like. The usage-amount of an alkali catalyst is about 0.01-1.0 mass% of the total preparation amount (dry matter conversion), Preferably it is about 0.05-0.5 mass%.
上記エステル化反応は、例えば攪拌機、加熱用のジャケット、邪魔板、不活性ガス吹き込み管、温度計および冷却器付き水分分離器などを備えた通常の反応容器に、ソルビトールまたはソルビトール分子内縮合物、脂肪酸、および触媒を供給して攪拌混合し、窒素または二酸化炭素などの任意の不活性ガス雰囲気下で、エステル化反応により生成する水を系外に除去しながら、所定温度で一定時間加熱して行われる。反応温度は通常、約180〜260℃の範囲、好ましくは約200〜250℃の範囲である。また、反応圧力条件は減圧下又は常圧下で、反応時間は約0.5〜15時間、好ましくは約1〜3時間である。反応の終点は、通常反応混合物の酸価を測定し、約10以下を目安に決められる。 The esterification reaction is carried out in a normal reaction vessel equipped with, for example, a stirrer, a heating jacket, a baffle plate, an inert gas blowing tube, a thermometer and a water separator with a condenser, etc., and sorbitol or sorbitol intramolecular condensate, A fatty acid and a catalyst are supplied and mixed with stirring. Under an inert gas atmosphere such as nitrogen or carbon dioxide, water generated by the esterification reaction is removed from the system and heated at a predetermined temperature for a certain period of time. Done. The reaction temperature is usually in the range of about 180 to 260 ° C, preferably in the range of about 200 to 250 ° C. The reaction pressure is under reduced pressure or normal pressure, and the reaction time is about 0.5 to 15 hours, preferably about 1 to 3 hours. The end point of the reaction is usually determined by measuring the acid value of the reaction mixture and about 10 or less.
エステル化反応終了後、必要に応じ、反応混合物中に残存する触媒を中和することができる。その際、エステル化反応の温度が200℃以上の場合は液温を約180〜200℃に冷却してから中和処理を行うのが好ましい。また反応温度が200℃以下の場合は、そのままの温度で中和処理を行って良い。中和後、その温度で好ましくは約0.5時間以上、更に好ましくは約1〜10時間放置する。未反応のソルビトールまたはソルビトール分子内縮合物が下層に分離した場合はそれを除去するのが好ましい。 After completion of the esterification reaction, the catalyst remaining in the reaction mixture can be neutralized as necessary. In that case, when the temperature of esterification reaction is 200 degreeC or more, it is preferable to neutralize after cooling liquid temperature to about 180-200 degreeC. Moreover, when reaction temperature is 200 degrees C or less, you may neutralize at the same temperature. After neutralization, it is allowed to stand at that temperature for about 0.5 hours or more, more preferably for about 1 to 10 hours. When unreacted sorbitol or sorbitol intramolecular condensate is separated into the lower layer, it is preferably removed.
本発明に用いられるソルビタン不飽和脂肪酸エステルは、そのエステル化率が60%未満であることが好ましく、50%未満であることがより好ましい。エステル化率が60%未満であると、特に精製パーム油などのパーム系油脂に対して十分に吸水性を付与することができるため好ましい。そのエステル化率(%)は下式により算出される。ここでエステル価および水酸基価は、「基準油脂分析試験法(I)」(社団法人 日本油化学会編)の[2.3.3-1996 エステル価]および[2.3.6-1996 ヒドロキシル価]に準じて測定される。 The sorbitan unsaturated fatty acid ester used in the present invention preferably has an esterification rate of less than 60%, and more preferably less than 50%. It is preferable for the esterification rate to be less than 60% because water absorption can be sufficiently imparted particularly to palm-based fats and oils such as refined palm oil. The esterification rate (%) is calculated by the following formula. Here, the ester value and the hydroxyl value are determined according to [2.3.3-1996 Ester Value] and [2.3.6-1996 Hydroxyl] of “Standard Oil and Fat Analysis Test Method (I)” (edited by the Japan Oil Chemists' Society). Value].
なお、ソルビタン不飽和脂肪酸エステルとしては、ソルビタンオレイン酸エステル(商品名:ポエムO−80V;エステル化率41.8%;理研ビタミン社製)などが商業的に製造および販売されており、本発明のクリーミング性向上剤にはこれらを用いることができる。 In addition, as sorbitan unsaturated fatty acid ester, sorbitan oleate (trade name: Poem O-80V; esterification rate 41.8%; manufactured by Riken Vitamin Co., Ltd.) and the like are commercially produced and sold. These can be used as the creaming improver.
本発明のクリーミング性向上剤の実施態様としては特に限定されないが、例えば、上記グリセリン有機酸脂肪酸エステルおよび/またはソルビタン不飽和脂肪酸エステルを油脂のクリーミング性向上剤として直接用いても良く、また上記グリセリン有機酸脂肪酸エステルおよび/またはソルビタン不飽和脂肪酸エステルをデキストリンや乳糖などの粉末化剤と共に水溶液とし、該水溶液を常法により乾燥・粉末化し、得られた粉末を油脂のクリーミング性向上剤としても良い。 The embodiment of the creaming property improver of the present invention is not particularly limited. For example, the glycerin organic acid fatty acid ester and / or sorbitan unsaturated fatty acid ester may be used directly as the fat creaming property improver. An organic acid fatty acid ester and / or sorbitan unsaturated fatty acid ester may be used as an aqueous solution together with a powdering agent such as dextrin or lactose, and the aqueous solution may be dried and powdered by a conventional method, and the resulting powder may be used as an oil cream improving agent. .
本発明のクリーミング性向上剤を含有する油脂組成物に使用される食用油脂としては、例えばパーム油、カカオ脂、ヤシ油、パーム核油等の植物性油脂並びに乳脂、牛脂、ラード、魚油、鯨油等の動物性油脂の他、菜種油、大豆油、ヒマワリ種子油、綿実油、落花生油、米糠油、コーン油、サフラワー油、オリーブ油、カポック油、ゴマ油、月見草油、パーム油、シア脂、サル脂、カカオ脂、ヤシ油、パーム核油等の植物性油脂並びに乳脂、牛脂、ラード、魚油、鯨油等の動物性油脂の単独又は混合油あるいはそれらの硬化、分別、エステル交換等を施した加工油脂が挙げられ、中でもパーム系油脂やカカオ脂、エステル交換油脂等が好ましく、パーム系油脂としては、天然パーム油を精製して得られる精製パーム油や天然パーム油を分別して得られるパームオレインあるいはパームステアリンが好ましい。 Examples of edible oils and fats used in the oil and fat composition containing the creaminess improver of the present invention include vegetable oils such as palm oil, cocoa butter, coconut oil, and palm kernel oil, and milk fat, beef tallow, lard, fish oil, and whale oil. Rapeseed oil, soybean oil, sunflower seed oil, cottonseed oil, peanut oil, rice bran oil, corn oil, safflower oil, olive oil, kapok oil, sesame oil, evening primrose oil, palm oil, shea fat, monkey fat , Vegetable oils such as cocoa butter, coconut oil, palm kernel oil and animal oils such as milk fat, beef tallow, lard, fish oil, whale oil, etc., alone or mixed oils, or processed oils and fats that have been cured, fractionated, transesterified, etc. Among them, palm-based fats and oils, cacao butter, transesterified fats and oils are preferable, and as palm-based fats and oils, purified palm oil and natural palm oil obtained by refining natural palm oil are fractionated. Resulting palm olein or palm stearin is preferred.
本発明の油脂組成物としては、例えば油中水型乳化物であるマーガリン、ファットスプレッド、および水分をほとんど含まないショートニングのような製品形態のものが挙げられる。ここでマーガリンは、油脂組成物中に占める油脂含有率が80重量%以上のものをいい、ファットスプレッドは80重量%未満のものをいう。 Examples of the oil and fat composition of the present invention include those in the form of products such as margarine, fat spread, and a shortening that hardly contains moisture, which are water-in-oil emulsions. Here, margarine means that the fat content in the fat composition is 80% by weight or more, and fat spread means less than 80% by weight.
本発明の油脂組成物の製造方法は特に限定されず、自体公知の方法を用いることができる。以下に、ショートニングの製造方法を例示する。例えば、食用油脂並びに上記グリセリン有機酸脂肪酸エステルおよび/またはソルビタン不飽和脂肪酸エステルを混合し、約50〜80℃、好ましくは約60〜70℃に加熱して溶解し、所望により酸化防止剤(例えば抽出トコフェロールなど)、着色料(例えばβ−カロテンなど)、香料(例えばミルクフレーバーなど)、上記グリセリン有機酸脂肪酸エステルおよびソルビタン不飽和脂肪酸エステル以外の乳化剤(例えばレシチンなど)などを添加する。得られた溶液を、組成物100g中約10〜15mlとなるよう窒素ガスまたは空気を吹き込みながら、送液ポンプで予冷器を通して急冷捏和装置に送液し、油脂の結晶化と練捏を連続的に行いショートニングを得る。得られたショートニングは、更に、約25〜30℃で24〜72時間テンパリングされるのが好ましい。 The manufacturing method of the oil-fat composition of the present invention is not particularly limited, and a method known per se can be used. Below, the manufacturing method of shortening is illustrated. For example, the edible fat and oil and the above glycerin organic acid fatty acid ester and / or sorbitan unsaturated fatty acid ester are mixed and dissolved by heating to about 50 to 80 ° C., preferably about 60 to 70 ° C., and optionally an antioxidant (for example, Extracted tocopherols, etc.), coloring agents (eg, β-carotene, etc.), flavors (eg, milk flavor, etc.), emulsifiers (eg, lecithin, etc.) other than the glycerin organic acid fatty acid ester and sorbitan unsaturated fatty acid ester, and the like are added. While blowing nitrogen gas or air so that the obtained solution becomes about 10 to 15 ml in 100 g of the composition, the solution is sent to a quenching kneader through a precooler with a liquid feed pump, and crystallization of fats and oils is continuously performed. To get shortening. The resulting shortening is preferably further tempered at about 25-30 ° C. for 24-72 hours.
マーガリンもまた上記急冷捏和装置を用いて製造される。即ち、食用油脂並びに上記グリセリン有機酸脂肪酸エステルおよび/またはソルビタン不飽和脂肪酸エステルを混合し、約50〜80℃、好ましくは約60〜70℃に加熱して溶解し、所望により酸化防止剤(例えば抽出トコフェロールなど)、着色料(例えばβ−カロテンなど)、香料(例えばミルクフレーバーなど)、上記グリセリン有機酸脂肪酸エステルおよびソルビタン不飽和脂肪酸エステル以外の乳化剤(例えばレシチンなど)などを添加して油相とする。一方、精製水に、所望により乳または乳製品(例えば全粉乳、脱脂粉乳など)、食塩、砂糖類、酸味料(例えばクエン酸など)などを加え、約50〜60℃に加熱して溶解し水相とする。次に、油相と水相を通常の攪拌・混合槽を用いて混合し、得られた混合液を送液ポンプで急冷捏和装置に送液し、油脂の結晶化と練捏を連続的に行いマーガリンを得る。また乳化工程をとらず、油相と水相をそれぞれ定量ポンプで急冷捏和装置に送液し、以下同様に処理しマーガリンを得ることもできる。得られたマーガリンは、更に、約25〜30℃で24〜72時間テンパリングされるのが好ましい。 Margarine is also produced using the above quench kneader. That is, the edible fat and oil and the above glycerin organic acid fatty acid ester and / or sorbitan unsaturated fatty acid ester are mixed and dissolved by heating to about 50 to 80 ° C., preferably about 60 to 70 ° C., and optionally an antioxidant (for example, Extracted tocopherol etc.), coloring agent (eg β-carotene etc.), flavoring (eg milk flavor etc.), emulsifier (eg lecithin etc.) other than the above glycerin organic acid fatty acid ester and sorbitan unsaturated fatty acid ester etc. And On the other hand, milk or dairy products (eg, whole milk powder, skim milk powder, etc.), salt, sugars, acidulants (eg, citric acid, etc.), etc. are added to purified water as desired, and heated to about 50-60 ° C. to dissolve. Let it be an aqueous phase. Next, the oil phase and the aqueous phase are mixed using a normal stirring / mixing tank, and the resulting mixture is fed to a quenching kneader with a feed pump to continuously crystallization and kneading of fats and oils. Go to and get margarine. Further, without taking the emulsification step, the oil phase and the water phase can be sent to a quenching kneader with a metering pump, respectively, and then treated in the same manner to obtain margarine. The obtained margarine is further preferably tempered at about 25-30 ° C. for 24-72 hours.
急冷捏和装置としては、例えばボテーター(ケメトロン社製)、パーフェクター(ゲルステンベルグ社製)、コンビネーター(シュローダー社製)、オンレーター(櫻製作所社製)、マーガリンプロセッサー(POWER POINT INTERNATIONAL社製)などが挙げられる。該装置は一般にAユニットとBユニットから構成され、Aユニットは管型の掻き取り式熱交換機からなっている。Bユニットは製品の種類、目的により構造の異なる管が用いられ、マーガリン、ファットスプレッドでは例えば中空管または内部に金網を設けた管などが、またショートニングでは管の内壁およびシャフトにピンを設けた混練機(ピンチューブ)などが用いられる。 Examples of the quenching and kneading device include a botator (manufactured by Chemetron), a perfector (manufactured by Gelstenberg), a combinator (manufactured by Schroeder), an onrator (manufactured by Sakai Seisakusho), and a margarine processor (manufactured by POWER POINT INTERNATIONAL). ) And the like. The apparatus is generally composed of an A unit and a B unit, and the A unit is composed of a tube-type scraping heat exchanger. The B unit uses tubes with different structures depending on the type and purpose of the product. For margarine and fat spread, for example, a hollow tube or a tube with a wire mesh inside, and for shortening, a pin is provided on the inner wall and shaft of the tube. A kneader (pin tube) or the like is used.
本発明の油脂組成物100質量%中のグリセリン有機酸脂肪酸エステルおよび/またはソルビタン不飽和脂肪酸エステルの含有量の合計は、0.05質量%〜10.0質量%であることが好ましく、0.1質量%〜5.0質量%であることがより好ましい。グリセリン有機酸脂肪酸エステルおよび/またはソルビタン不飽和脂肪酸エステルの含有量の合計の合計が0.05質量%未満であると、油脂組成物のクリーミング速度および吸水速度の向上が不十分であり、また、10.0質量%を越えると、油脂組成物の風味に悪影響を与える他、経済的にも好ましくない。 The total content of glycerin organic acid fatty acid ester and / or sorbitan unsaturated fatty acid ester in 100% by mass of the oil and fat composition of the present invention is preferably 0.05% by mass to 10.0% by mass, and It is more preferable that it is 1 mass%-5.0 mass%. When the total content of the glycerin organic acid fatty acid ester and / or sorbitan unsaturated fatty acid ester is less than 0.05% by mass, the improvement of the creaming rate and the water absorption rate of the fat composition is insufficient. If it exceeds 10.0% by mass, the flavor of the oil and fat composition is adversely affected, and it is not preferable economically.
本発明の油脂組成物(ショートニング)には、食品添加物として、上記の酸化防止剤、着色料、香料、乳化剤の他に、酸化防止助剤(例えばクエン酸など)、消泡剤(例えばシリコーン樹脂など)などを含有させることができる。 In the oil and fat composition (shortening) of the present invention, as a food additive, in addition to the above-mentioned antioxidants, colorants, fragrances, and emulsifiers, antioxidant assistants (for example, citric acid), antifoaming agents (for example, silicone) Resin) and the like.
また、本発明の油脂組成物(マーガリン)には、食品添加物として、上記の酸化防止剤、着色料、香料、乳化剤、酸味料の他に、乳化安定剤(例えばカゼインナトリウム、ポリリン酸ナトリウムなど)、調味料(例えばL−グルタミン酸ナトリウムなど)、糊料(例えばカラギナン、キサンタンガムなど)、保存料(例えばソルビン酸カリウムなど)、強化剤(例えばビタミンA脂肪酸エステルなど)などを含有させることができる。 In addition, in the oil and fat composition (margarine) of the present invention, as a food additive, in addition to the above-mentioned antioxidant, colorant, fragrance, emulsifier, acidulant, an emulsion stabilizer (for example, sodium caseinate, sodium polyphosphate, etc.) ), Seasonings (such as sodium L-glutamate), pastes (such as carrageenan, xanthan gum), preservatives (such as potassium sorbate), reinforcing agents (such as vitamin A fatty acid esters), and the like. .
本発明のクリーミング性向上剤を含有する油脂組成物は、クリーミング速度および吸水速度に優れるため、パン・菓子類(例えば、パン、ケーキ、クッキー、ビスケット等)を効率良く生産するために好適に使用される。ここで、本発明の目的とするクリーミング速度に優れた油脂組成物とは、下記クリーミング速度評価方法により油脂組成物を攪拌泡気させたとき、クリーミング価が200に達するまでの時間が8分未満であり、且つクリーミング価が250に達するまでの時間が12分未満のものをいう。 The oil and fat composition containing the creaming property improver of the present invention is excellent in creaming speed and water absorption speed, and is therefore preferably used for efficiently producing bread and confectionery (for example, bread, cakes, cookies, biscuits, etc.). Is done. Here, the oil / fat composition excellent in creaming speed as an object of the present invention is less than 8 minutes until the creaming number reaches 200 when the oil / fat composition is stirred and bubbled by the following creaming speed evaluation method. And the time until the creaming value reaches 250 is less than 12 minutes.
<クリーミング速度評価方法>
ホイッパーを装着した卓上ミキサー(製品名:キッチンエイド・ミキサー;Kitchen Aid社製)を用いて、予め20℃に温調した油脂組成物400gを撹拌して起泡させる(速度数「6」;ミキサーのボールは20℃循環水冷却;室温25℃)。次いで、攪拌しながら、経時的にクリーム状のサンプルのクリーミング価を次式により求め、攪拌を開始してからクリーミング価が200および250に達するまでの時間を測定する。
<Creaming speed evaluation method>
Using a tabletop mixer (product name: Kitchen Aid Mixer; manufactured by Kitchen Aid) equipped with a whipper, 400 g of an oil / fat composition preliminarily adjusted to 20 ° C. is agitated to foam (speed number “6”; mixer) The balls are cooled at 20 ° C with circulating water; room temperature 25 ° C). Next, the creaming value of the cream-like sample is obtained with the following formula while stirring, and the time from the start of stirring until the creaming value reaches 200 and 250 is measured.
また、本発明の目的とする吸水速度に優れた油脂組成物とは、下記測定方法により油脂組成物に水を抱き込ませるのに要する時間が3分未満のものをいう。 Moreover, the oil and fat composition excellent in the water absorption speed which is the object of the present invention refers to an oil and fat composition which takes less than 3 minutes to incorporate water into the oil and fat composition by the following measurement method.
<吸水速度評価方法>
ホイッパーを装着した卓上ミキサー(製品名:キッチンエイド・ミキサー;Kitchen Aid社製)を用いて、予め20℃に調温した油脂組成物400gを12分間撹拌して起泡させる(速度数「6」;ミキサーのボールは20℃循環水冷却;室温25℃)。次いで、攪拌を継続しながら、水300mLを一度に加え、水を加えてから水が完全に混和するまでに要する時間を測定する。
<Water absorption rate evaluation method>
Using a tabletop mixer (product name: Kitchen Aid Mixer; manufactured by Kitchen Aid) equipped with a whipper, 400 g of an oil / fat composition preliminarily adjusted to 20 ° C. is stirred for 12 minutes to foam (speed number “6”) The bowl of the mixer is 20 ° C circulating water cooled; room temperature 25 ° C). Next, while continuing stirring, 300 mL of water is added all at once, and the time required from the addition of water to the complete mixing of the water is measured.
なお、吸水性のうち、油脂組成物が卵を抱き込む性質に着目したものを特に吸卵性という。本発明の目的とする油脂組成物は、下記吸卵速度評価方法により油脂組成物に卵を抱き込ませるのに要する時間が3分未満のものをいう。 In addition, among water absorption, what paid attention to the property in which an oil-and-fat composition embraces an egg is called egg-absorbing property especially. The oil / fat composition as an object of the present invention refers to an oil / fat composition that takes less than 3 minutes to embed an egg in the oil / fat composition by the following method for evaluating the egg-absorption rate.
<吸卵速度評価方法>
ホイッパーを装着した卓上ミキサー(製品名:キッチンエイド・ミキサー;Kitchen Aid社製)を用いて、予め20℃に調温した油脂組成物400gを12分間撹拌して起泡させる(速度数「6」;ミキサーのボールは20℃循環水冷却;室温25℃)。次いで、攪拌を継続しながら、全卵液300gを一度に加え、全卵液を加えてから全卵液が完全に混和するまでに要する時間を測定する。
<Egg sucking speed evaluation method>
Using a tabletop mixer (product name: Kitchen Aid Mixer; manufactured by Kitchen Aid) equipped with a whipper, 400 g of an oil / fat composition preliminarily adjusted to 20 ° C. is stirred for 12 minutes to foam (speed number “6”) The bowl of the mixer is 20 ° C circulating water cooled; room temperature 25 ° C). Then, while continuing stirring, 300 g of whole egg liquid is added at once, and the time required from the addition of the whole egg liquid to the complete mixing of the whole egg liquid is measured.
以下に本発明を実施例に基づいてより具体的に説明するが、本発明はこれらに限定されるものではない。 Hereinafter, the present invention will be described more specifically based on examples, but the present invention is not limited thereto.
[ショートニングの製造および評価]
(1)ショートニングの製造
精製パーム油(商品名:RPO;植田製油社製)4000gに表1に示す乳化剤計20gをクリーミング性改良剤としてそれぞれ加えて溶解し、約70℃に加温した。得られた混合物をマーガリンプロセッサー(POWER POINT INTERNATIONAL社製)に供給して急冷捏和した。次いで、この混合物を25℃で24時間テンパリング処理した後、10℃で18時間保存し、ショートニング2000g(試料No.1〜8)をそれぞれ得た。この内、試料No.1〜4は本発明に係る実施例であり、試料No.5〜8はそれらに対する比較例である。
[Manufacturing and evaluation of shortening]
(1) Production of shortening 20 g of emulsifiers shown in Table 1 were added to 4000 g of purified palm oil (trade name: RPO; manufactured by Ueda Oil Co., Ltd.) as a creaming improver, respectively, and heated to about 70 ° C. The obtained mixture was supplied to a margarine processor (manufactured by POWER POINT INTERNATIONAL) and rapidly cooled and kneaded. Subsequently, this mixture was tempered at 25 ° C. for 24 hours and then stored at 10 ° C. for 18 hours to obtain 2000 g of shortening (sample Nos. 1 to 8). Among these, sample no. 1 to 4 are examples according to the present invention. 5-8 are comparative examples for them.
なお、表1に示す乳化剤のうち、ポリグリセリン脂肪酸エステル(試作品)は、下記製造例に従い製造した。 In addition, among the emulsifiers shown in Table 1, polyglycerin fatty acid ester (prototype) was produced according to the following production example.
[製造例]
撹拌機、温度計、ガス吹込管および水分離器を取り付けた1Lの四つ口フラスコに、ポリグリセリン(商品名:ポリグリセリン#750;平均重合度10;阪本薬品工業社製)162.4g、パルミチン酸とステアリン酸の混合脂肪酸(商品名:ステアリン酸65;ステアリン酸含量65%、パルミチン酸含量35%;ミヨシ油脂社製)308.0g、オレイン酸とリノール酸が主体の混合脂肪酸(商品名:ルナックO−V;オレイン酸含有量約79%;リノール酸含有量約11%;パルミチン酸含有量約6%;ステアリン酸含有量約2%;花王社製)249.6gおよびラウリン酸(商品名:ルナックL−50;花王社製)を仕込み、窒素ガス気流中、反応液の酸価が20以下になるまで240℃で約8時間エステル化反応を行い、さらに過剰な脂肪酸の除去を目的として窒素ガスを吹き込む処理を約2時間行った。得られた反応液を約180℃まで冷却し、その温度で約1時間放置した後、分離した未反応のポリグリセリンを含むポリオールを除去し、ポリグリセリン脂肪酸エステル(試作品)約740gを得た。
[Production example]
In a 1 L four-necked flask equipped with a stirrer, thermometer, gas blowing tube and water separator, polyglycerin (trade name: polyglycerin # 750; average polymerization degree 10; manufactured by Sakamoto Yakuhin Kogyo Co., Ltd.), 162.4 g, Mixed fatty acid of palmitic acid and stearic acid (trade name: stearic acid 65; stearic acid content 65%, palmitic acid content 35%; manufactured by Miyoshi Oil & Fats Co., Ltd.) 308.0 g, mixed fatty acid mainly composed of oleic acid and linoleic acid (trade name) Lunac O-V; oleic acid content of about 79%; linoleic acid content of about 11%; palmitic acid content of about 6%; stearic acid content of about 2%; manufactured by Kao Corporation) and lauric acid (commercial product) Name: LUNAC L-50; manufactured by Kao Corporation), and in an nitrogen gas stream, an esterification reaction is performed at 240 ° C. for about 8 hours until the acid value of the reaction solution becomes 20 or less. The process of blowing nitrogen gas for the purpose of removal of over - fatty acids was carried out for about 2 hours. The obtained reaction liquid was cooled to about 180 ° C. and left at that temperature for about 1 hour, and then the separated polyol containing unreacted polyglycerin was removed to obtain about 740 g of a polyglycerin fatty acid ester (prototype). .
(2)クリーミング速度の評価
ホイッパーを装着した卓上ミキサー(製品名:キッチンエイド・ミキサー;Kitchen Aid社製)でショートニング(試料No.1〜8)各400gを撹拌して起泡させた(速度数「6」;ミキサーのボールは20℃循環水冷却;室温25℃)。次いで、攪拌を開始してから3分、6分、9分および12分の時点でのショートニングのクリーミング価を次式により求めた。これらクリーミング価に基づき、攪拌を開始してからクリーミング価(CV)が200および250に達するまでの時間(ホイップ時間)を算出した。
(2) Evaluation of creaming speed 400 g of each shortening (sample No. 1-8) was stirred and foamed with a tabletop mixer (product name: kitchen aid mixer; manufactured by Kitchen Aid) equipped with a whipper (speed number) “6”; the mixer bowl was cooled at 20 ° C. with circulating water; room temperature 25 ° C.). Next, the shortening creaming number at the time of 3 minutes, 6 minutes, 9 minutes, and 12 minutes from the start of stirring was determined by the following equation. Based on these creaming numbers, the time (whipping time) from the start of stirring until the creaming number (CV) reached 200 and 250 was calculated.
(3)吸水速度の評価
ホイッパーを装着した卓上ミキサー(製品名:キッチンエイド・ミキサー;Kitchen Aid社製)を用いて、予め20℃に調温した油脂組成物400gを12分間撹拌して起泡させた(速度数「6」;ミキサーのボールは20℃循環水冷却;室温25℃)。次いで、攪拌を継続しながら、水300mLを一度に加え、水を加えてから水が完全に混和するまでに要した時間(吸水時間)を測定した。なお、水を加えてから3分が経過しても完全に混和しない場合は測定を中止した。
(3) Evaluation of water absorption rate Using a tabletop mixer (product name: Kitchen Aid Mixer; manufactured by Kitchen Aid) equipped with a whipper, 400 g of an oil / fat composition preliminarily adjusted to 20 ° C. was stirred for 12 minutes to foam (Speed number "6"; mixer balls cooled at 20 ° C circulating water; room temperature 25 ° C). Next, while continuing stirring, 300 mL of water was added at once, and the time (water absorption time) required from the addition of water to the complete mixing of water was measured. In addition, the measurement was stopped when it was not completely mixed even if 3 minutes passed after adding water.
(4)吸卵速度の評価
ホイッパーを装着した卓上ミキサー(製品名:キッチンエイド・ミキサー;Kitchen Aid社製)を用いて、予め20℃に調温した油脂組成物400gを12分間撹拌して起泡させた(速度数「6」;ミキサーのボールは20℃循環水冷却;室温25℃)。次いで、攪拌を継続しながら、全卵液300gを一度に加え、全卵液を加えてから全卵液が完全に混和するまでに要した時間(吸卵時間)を測定した。なお、全卵液を加えてから3分が経過しても完全に混和しない場合は測定を中止した。
(4) Evaluation of egg sucking speed Using a tabletop mixer (product name: Kitchen Aid Mixer; manufactured by Kitchen Aid) equipped with a whipper, 400 g of an oil / fat composition adjusted to 20 ° C. in advance was stirred for 12 minutes. It was bubbled (speed number “6”; the bowl of the mixer was 20 ° C. circulating water cooling; room temperature 25 ° C.). Next, while stirring was continued, 300 g of the whole egg solution was added at once, and the time required from the addition of the whole egg solution until the whole egg solution was completely mixed (the egg sucking time) was measured. In addition, the measurement was stopped when it did not mix completely even if 3 minutes passed after adding the whole egg liquid.
(5)結果
上記(2)〜(4)の評価について結果を表2に示す。
(5) Results Table 2 shows the results of the evaluations (2) to (4) above.
表2から明らかなように、実施例のショートニング(試料No.1〜4)は、クリーミング価が200に達するまでのホイップ時間が8分未満であり、クリーミング価が250に達するまでのホイップ時間が12分未満であり、吸水時間が3分未満であり、且つ吸卵時間が3分未満であった。即ち、実施例のショートニングは、いずれの評価項目においても優れたものであった。これに対し、比較例のショートニング(試料No.5〜8)は、少なくとも1以上の評価項目において実施例のものに比べて劣っていた。 As is apparent from Table 2, the shortening of the examples (Sample Nos. 1 to 4) has a whipping time of less than 8 minutes until the creaming value reaches 200, and a whipping time until the creaming value reaches 250. It was less than 12 minutes, the water absorption time was less than 3 minutes, and the egg sucking time was less than 3 minutes. That is, the shortening of the example was excellent in all evaluation items. On the other hand, the shortening of the comparative example (sample Nos. 5 to 8) was inferior to that of the example in at least one evaluation item.
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