JPH0318669B2 - - Google Patents
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- Publication number
- JPH0318669B2 JPH0318669B2 JP58086359A JP8635983A JPH0318669B2 JP H0318669 B2 JPH0318669 B2 JP H0318669B2 JP 58086359 A JP58086359 A JP 58086359A JP 8635983 A JP8635983 A JP 8635983A JP H0318669 B2 JPH0318669 B2 JP H0318669B2
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- Prior art keywords
- oil
- fat
- water
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- weight
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- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- Edible Oils And Fats (AREA)
- Colloid Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
本発明は油中水中油型二重乳化油脂組成物およ
びその製造方法に関するものである。ここで云う
油中水中油型二重乳化油脂組成物とは、最内相油
脂を中間水相で包み、さらにこれを最外相油脂で
包んだ可食性の油脂組成物であり、主に代用バタ
ー、マーガリン、フイリング、トツピング等に供
されるものである。
油中水中油型二重乳化油脂組成物についてはこ
れまでいくつかの特許が出ており、例えば英国特
許第614925号、特開昭49−31707号、特公昭54−
15682号などがある。その中で二重乳化油脂組成
物が通常の油中水型油脂組成物に比較し優れてい
る点として、内外相の油脂の種類を適当に変える
ことにより、延展性や保型性などの物理特性およ
び口どけなどが改良される点が挙げられている。
本発明者らは本発明を完成させる過程において、
二重乳化油脂組成物の優れている点としてこれら
の他に特に最内相油脂中に香料等の呈味物質を入
れるとコク味が付与され、呈味性が著しく向上す
ることを知見した。
さて、以上のように二重乳化油脂組成物は、通
常の油中水型油脂組成物に比較して延展性や保型
性などの物理特性、口どけ及び呈味性において優
れているが、これはあくまで得られた最終製品が
目的とする構造になつている場合に得られる効果
であつて、製造過程において仕込んだ最内相油脂
の多くが最外相油脂と合一してしまう場合には、
得られる最終製品の特徴はむしろ油中水型油脂組
成物の特徴に近いものとなつてしまう。この意味
から、仕込んだ最内相油脂のうちどれくらいの量
が最終製品の最内相油脂として存在するかが重要
な問題となるが、本発明者らはこの点を明確にす
るために二重乳化油脂組成物の生成率という概念
を用いる(以下、単に生成率と称する)。
すなわち、二重乳化油脂組成物を製造するにあ
たり、その最内相油脂として仕込んだ油脂の最終
製品中における重量パーセントをa%とし、また
最終製品中における実際の最内相油脂の量を同じ
くb%とした場合、(b/a)×100%を生成率と
称する。従つて、製造過程においてもし最内相油
脂のうち最外相油脂へ移行してしまうものが全く
無ければ、a=bとなり生成率は100%となる。
逆に内外相油脂が合一してしまい最内相油脂が全
て最外相油脂へと移行してしまう場合には、b=
0となり生成率は0%となり、その製品の特徴は
通常の油中水型乳化油脂組成物の特徴と同じにな
つてしまう。従つて、できるだけ生成率を上げる
ことが二重乳化油脂組成物を製造するにあたり、
たいへん重要な課題である。
二重乳化油脂組成物の他の特徴として、内外相
の油脂の種類を変えられるということが挙げられ
る。これは、例えば比較的高温における保型性を
付与させたい場合には最内相油脂に高融点の油脂
を用いるのが望ましく、また口どけを良くしたい
場合には最内相油脂として低融点の油脂を用いる
のが望ましいなど、目的とする最終製品に応じて
内外相油脂を使い分けることができるということ
である。従つて、最内相油脂として低融点油脂を
用いても、あるいは高融点油脂を用いても、油脂
の種類に拘わらず高い生成率が得られるというこ
とが二重乳化油脂組成物を製造するにあたり極め
て重要な課題であると言える。
二重乳化油脂組成物を製造するに当つてもう一
つ重要な課題としては、口中の温度において、乳
化が破壊されやすくあるべきということである。
ここで言う乳化の破壊とは、油中水中油型二重乳
化油脂組成物が内相の水中油型乳化物と最外相油
脂とに分離することを云う。何故に乳化が破壊さ
れやすくあるべきかと言うと、呈味物質の多くは
水相中にあるため、口中に入つたとき呈味性が優
れるためには乳化がすみやかに破壊され、水相物
質が容易に舌の感覚器官に触れる必要があるから
である。
以上述べた様に、二重乳化油脂組成物を製造す
るにあたり重要な課題としては、最内相油脂の種
類に拘わらず高い生成率が得られると共に、口中
の温度において乳化が破壊されやすいということ
である。
本発明はこれらの点について優れた新規な油中
水中油型二重乳化油脂組成物およびその製法を提
供するものであり、以下にその内容を詳述する。
本発明による油中水中油型二重乳化油脂組成物
の製造方法は、まず内相の水中油型乳化物を作成
後、この乳化物を最外相油脂中に混合分散させる
ことによる。
内相の水中油型乳化物の作成法は、まず最内相
油脂をその融点以上の温度に加熱溶解し、必要に
応じてこの中に香料や着色剤を加えるが乳化剤は
全く用いないのが望ましい。使用し得る油脂とし
ては大豆油、コーン油、コメ油、ナタネ油等の液
体油及び動植物油脂の硬化油等の固体油がその種
類、融点、固体脂含有率に拘わらず、各々単独も
しくは混合物として用いることが可能である。
続いて、この最内相油脂を水相中に乳化させる
が、水相成分としては水、カゼインナトリウム、
水溶性レシチン及び必要に応じて糖類、食塩、脱
脂乳、練乳等の呈味物質を用いる。
カゼインナトリウムの使用量としては水中油型
乳化物に対し1.5〜5.0重量%添加することが好ま
しく、更に望ましくは2.0〜4.5重量%添加するこ
とが良い。カゼインナトリウムの使用量が1.5重
量%未満では、できた乳化物の安定性が劣り、生
成率が下がつてしまう。逆にカゼインナトリウム
の使用量が5.0重量%を超える場合には、できた
乳化物の粘度が非常に高くなり、取り扱いが難し
くなつてしまう。
さらに、生成率を高く維持するために水溶性レ
シチンをカゼインナトリウム100重量部に対して
3〜15重量部使用するのが好ましく、更に望まし
くは10〜13重量部用いるのが良い。
これらを配合した水相を撹拌、加熱して充分内
容物を溶解せしめ、続いてこの中に撹拌しながら
加熱溶解した最内相油脂を徐々に加えて70〜80℃
に乳化する。
加える最内相油脂量はこの水中油型乳化物に対
し15〜65重量%用いることが好ましく、更に好ま
しくは45〜55重量%用いるのが良い。
得られた乳化物をホモジナイザーに150Kg/cm2
の圧力下で2回通し、油脂粒径を1〜3μmに調整
したのち、放冷もしくは熱交換器を用いて15〜25
℃に冷却する。
一方、最外相油脂をその融点以上の温度にて加
熱溶解せしめ、これに乳化剤及び必要に応じて香
料、着色剤等を添加し、溶解後ボテーター等の急
冷可塑化装置を用いて可塑化する。
用いる最外相油脂は融点が25〜35℃で常温で固
体であることが口どけ面で好ましいが、その種類
は問わない。
使用する乳化剤はソルビタントリ脂肪酸エステ
ル、好ましくはソルビタントリステアレート又は
ソルビタントリオレートを使用し、油中水中油型
二重乳化物全体に対し0.1〜2.0重量%用いるのが
好ましく、特に0.5〜1.5重量%用いるのが望まし
い。使用量が0.1重量%未満の場合には、二重乳
化物を製造するに当たり乳化力が劣り、また2.0
重量%を超えて用いると風味を損なう恐れがあ
る。最外相油脂を急冷可塑化後、温度を15〜25℃
に調整し、これに先に15〜25℃に冷却した水中油
型乳化物を加え、混合・撹拌して油中水中油型二
重乳化油脂組成物を得る。
混合時の温度が比較的高い場合には、水中油型
乳化物が最外相油脂中に分散・乳化されるに必要
な撹拌所要時間は比較的短かくなり、水中油型乳
化物の粒径は比較的大きくなる。一方、混合時の
温度が比較的低い場合にはその逆の現象が起こる
ので、混合時の温度選定にあたつては用いる混合
機の種類や目的に応じて適宜決めるのが良い。
混合時間は、もはや水相の分離が全く認められ
ぬ程度まで充分長くとる必要があり、その所要時
間は先に述べたように混合時の温度に依存する。
一般的に得られる最終製品中に分散している水中
油型乳化物は、混合機にもよるがおよそ5〜
25μmである。
混合方法はバツチ式でも連続式でも良い。連続
式の場合は、最外相油脂の急冷可塑化に連続して
行なうと製造にあたつてムダが少なく好適であ
る。
用いる水中油型乳化物の量は、最終的に得られ
る二重乳化油脂組成物に対して30〜70重量%用い
るが、更に好ましくは40〜60重量%用いるのが良
い。
内相の水中油型乳化物と最外相油脂との混合は
50〜60℃の高温において混合乳化し、しかる後に
ボテーター等の急冷可塑化装置を用いて急冷可塑
化し、二重乳化油脂組成物を得ることも可能であ
るが、50〜60℃における乳化が比較的不安定であ
るため、乳化方法を工夫することが好ましい。
本発明による油中水中油型二重乳化油脂組成物
は、最内相油脂の種類に拘わらず高い生成率が得
られると共に、常温以下の温度では安定な乳化を
保ち、口中の温度においては乳化が破壊されやす
い性質を持つ。このような性質は本発明における
水相中の乳化剤と最外相油中の乳化剤を共に用い
る場合にはじめて得られるものであり、このうち
の一方が欠けても満足のいく結果は得られない。
本発明を更に詳細に説明する為、以下に実施例
を示すが、本発明はこれらに限定されるものでは
ない。
実施例 1
下記配合にて油中水中油型二重乳化油脂組成物
を得た。
The present invention relates to an oil-in-water type double emulsified fat composition and a method for producing the same. The oil-in-water-type double emulsified fat composition referred to here is an edible fat composition in which the innermost phase fat is wrapped in an intermediate aqueous phase, which is further wrapped in the outermost fat phase, and is mainly used as a butter substitute. , margarine, fillings, toppings, etc. Several patents have been issued regarding oil-in-water type double emulsified oil and fat compositions, such as British Patent No. 614925, JP-A-49-31707, and JP-B-Sho 54-
There are issues such as No. 15682. Among them, double emulsified oil compositions are superior to ordinary water-in-oil oil compositions because they can improve physical properties such as spreadability and shape retention by appropriately changing the types of oils and fats in the inner and outer layers. It is said that the properties and melt-in-the-mouth properties are improved.
In the process of completing the present invention, the inventors
In addition to these advantages, the double emulsified oil and fat compositions have also been found to be particularly advantageous in that when a flavoring substance such as a flavoring agent is added to the innermost phase of the oil, a rich flavor is imparted and the taste properties are significantly improved. Now, as described above, double emulsified oil and fat compositions are superior to ordinary water-in-oil oil and fat compositions in terms of physical properties such as spreadability and shape retention, as well as melt-in-the-mouth texture and taste. This is only an effect that can be obtained when the final product obtained has the desired structure, and if much of the innermost phase fat mixed in during the manufacturing process is combined with the outermost phase fat. ,
The characteristics of the final product obtained are rather similar to those of a water-in-oil oil composition. In this sense, an important issue is how much of the charged innermost phase fat will be present as the innermost phase fat in the final product. The concept of production rate of the emulsified oil and fat composition is used (hereinafter simply referred to as production rate). That is, when producing a double emulsified fat composition, the weight percent of the fat and oil charged as the innermost phase oil in the final product is a%, and the actual amount of the innermost phase fat and oil in the final product is also b. %, (b/a)×100% is called the production rate. Therefore, in the manufacturing process, if there is no part of the innermost phase fat that migrates to the outermost phase fat and oil, a=b and the production rate will be 100%.
On the other hand, if the inner and outer phase fats and oils coalesce and all the innermost phase fats and oils transfer to the outermost phase fats, b=
0, the production rate becomes 0%, and the characteristics of the product become the same as those of ordinary water-in-oil emulsified fat compositions. Therefore, when producing a double emulsified fat composition, it is important to increase the production rate as much as possible.
This is a very important issue. Another feature of the double emulsified fat composition is that the types of fats and oils in the inner and outer phases can be changed. For example, if you want to impart shape retention at relatively high temperatures, it is desirable to use an oil with a high melting point as the innermost phase, and if you want to improve the melt-in-your-mouth texture, use a low-melting point oil as the innermost phase. This means that it is possible to use different types of fats and oils depending on the desired final product, such as the use of fats and oils. Therefore, whether a low melting point fat or a high melting point fat is used as the innermost phase fat, a high production rate can be obtained regardless of the type of fat when producing a double emulsified fat composition. This can be said to be an extremely important issue. Another important issue in producing double emulsified oil and fat compositions is that the emulsification should be easily broken down at the temperature in the mouth.
The destruction of emulsification here refers to the separation of an oil-in-water type double emulsified oil/fat composition into an oil-in-water type emulsion in the inner phase and an outermost phase oil/fat. The reason why emulsions should be easily destroyed is that most of the taste substances are in the aqueous phase, so in order for the taste to be excellent when it enters the mouth, the emulsification must be destroyed quickly and the water phase substances must be destroyed. This is because it is necessary to easily touch the sensory organs of the tongue. As mentioned above, the important issues in producing double emulsified oil and fat compositions are that a high production rate can be obtained regardless of the type of innermost phase oil, and that the emulsification is easily destroyed at the temperature in the mouth. It is. The present invention provides a novel oil-in-water type double emulsified fat composition that is excellent in these respects and a method for producing the same, the details of which are detailed below. The method for producing an oil-in-water-type double emulsified fat composition according to the present invention involves first preparing an oil-in-water emulsion of the inner phase, and then mixing and dispersing this emulsion in the outermost phase fat and oil. The method for creating an oil-in-water emulsion for the inner phase is to first heat and dissolve the innermost phase oil to a temperature above its melting point, and add fragrances and coloring agents to this as necessary, but it is best not to use an emulsifier at all. desirable. Examples of oils and fats that can be used include liquid oils such as soybean oil, corn oil, rice oil, and rapeseed oil, and solid oils such as hydrogenated animal and vegetable oils, each alone or as a mixture, regardless of their type, melting point, and solid fat content. It is possible to use Next, this innermost phase oil and fat is emulsified into an aqueous phase, and the aqueous phase components include water, sodium caseinate,
Water-soluble lecithin and, if necessary, sugars, salt, skim milk, condensed milk, and other flavoring substances are used. The amount of sodium caseinate used is preferably 1.5 to 5.0% by weight, more preferably 2.0 to 4.5% by weight, based on the oil-in-water emulsion. If the amount of sodium caseinate used is less than 1.5% by weight, the stability of the resulting emulsion will be poor and the production rate will decrease. On the other hand, if the amount of sodium caseinate used exceeds 5.0% by weight, the viscosity of the resulting emulsion becomes extremely high, making it difficult to handle. Furthermore, in order to maintain a high production rate, it is preferable to use 3 to 15 parts by weight of water-soluble lecithin per 100 parts by weight of sodium caseinate, and more preferably 10 to 13 parts by weight. The aqueous phase containing these ingredients is stirred and heated to sufficiently dissolve the contents, and then the innermost phase oil and fat, which has been heated and dissolved while stirring, is gradually added to the mixture at 70 to 80°C.
to emulsify. The amount of innermost phase oil and fat to be added is preferably 15 to 65% by weight, more preferably 45 to 55% by weight, based on the oil-in-water emulsion. 150Kg/cm 2 of the obtained emulsion in a homogenizer
After adjusting the oil particle size to 1-3μm by passing it twice under the pressure of
Cool to ℃. On the other hand, the outermost phase fat is heated and melted at a temperature above its melting point, an emulsifier and, if necessary, a fragrance, a coloring agent, etc. are added thereto, and after melting, it is plasticized using a rapid cooling plasticizing device such as a votator. It is preferable that the outermost phase oil or fat used has a melting point of 25 to 35°C and is solid at room temperature in terms of melting in the mouth, but the type thereof is not limited. The emulsifier to be used is sorbitan trifatty acid ester, preferably sorbitan tristearate or sorbitan triolate, and it is preferably used in an amount of 0.1 to 2.0% by weight, particularly 0.5 to 1.5% by weight, based on the entire oil-in-water-in-oil double emulsion. It is preferable to use %. If the amount used is less than 0.1% by weight, the emulsifying power will be poor when producing a double emulsion;
If used in excess of % by weight, the flavor may be impaired. After rapidly cooling and plasticizing the outermost phase oil, the temperature is increased to 15 to 25℃.
The oil-in-water emulsion previously cooled to 15 to 25°C is added thereto, and mixed and stirred to obtain an oil-in-water oil-in-water double emulsified fat composition. When the temperature during mixing is relatively high, the stirring time required for the oil-in-water emulsion to be dispersed and emulsified in the outermost phase of fat is relatively short, and the particle size of the oil-in-water emulsion is Becomes relatively large. On the other hand, when the temperature during mixing is relatively low, the opposite phenomenon occurs, so when selecting the temperature during mixing, it is best to select the temperature appropriately depending on the type of mixer used and the purpose. The mixing time must be long enough to such an extent that no separation of the aqueous phase can be observed, and the required time depends on the temperature at the time of mixing, as mentioned above.
Generally, the oil-in-water emulsion dispersed in the final product is approximately 5 to
It is 25μm. The mixing method may be either batch or continuous. In the case of a continuous type, it is preferable to carry out the rapid cooling plasticization of the outermost phase oil and fat continuously, since there is less waste during production. The amount of oil-in-water emulsion used is 30 to 70% by weight, more preferably 40 to 60% by weight, based on the double emulsified fat composition finally obtained. Mixing of the inner phase oil-in-water emulsion and the outermost phase oil and fat is
It is also possible to obtain a double emulsified oil and fat composition by mixing and emulsifying at a high temperature of 50 to 60°C and then rapidly cooling and plasticizing using a rapid cooling and plasticizing device such as a votator, but emulsification at 50 to 60°C is comparatively Because of the physical instability, it is preferable to devise an emulsification method. The oil-in-water type double emulsified fat composition according to the present invention can obtain a high production rate regardless of the type of innermost phase fat, maintain stable emulsification at temperatures below room temperature, and emulsify at temperatures in the mouth. has the property of being easily destroyed. Such properties can only be obtained in the present invention when the emulsifier in the aqueous phase and the emulsifier in the outermost oil phase are used together, and even if one of them is missing, satisfactory results cannot be obtained. Examples are shown below to explain the present invention in more detail, but the present invention is not limited thereto. Example 1 An oil-in-water-type double emulsified fat composition was obtained with the following formulation.
【表】【table】
【表】
まず、中間水相を加熱溶解せしめ、これに撹拌
を続けながら加熱溶解した最内相油脂を徐々に加
え、70〜80℃にて約10分間乳化した。
続いて、この乳化物を圧力150Kg/cm2下でホモ
ジナイザーに2回通し、粒径1〜3μmの微細な水
中油型乳化物とした。この乳化物を容器ごと20℃
まで放冷した。
一方、最外相を約70℃にて溶解し、これを40℃
まで冷却したのち、ボテーターで約20℃まで急冷
可塑化した。
得られた最外相中に前記水中油型乳化物を4対
6の割合で20℃にて撹拌しながら添加し、離水が
全く認められなくなるまで撹拌した。得られた油
中水中油型の二重乳化油脂組成物の生成率は69%
であつた。
また、口中の温度における乳化の破壊されやす
さを見るため、得られた油脂を37℃に昇温し、
300c.c.目盛付遠沈管にすばやく取り、1000rpmで
10分間遠心分離を行ない分離の様子を観察したと
ころ、全体の76%に当たる部分が最外相油脂と内
相水中油型乳化物とに分離した。
尚、この油中水中油型乳化油脂組成物を試食し
たところ、乳製品を全く使用していないにも拘わ
らず、ミルク的な呈味性があつた。
実施例 2
下記配合にて、実施例1と全く同様の操作に
て、油中水中油型二重乳化油脂組成物を得た。[Table] First, the intermediate aqueous phase was heated and dissolved, and the heated and dissolved innermost phase fat and oil was gradually added to this while continuing to stir, and emulsified at 70 to 80°C for about 10 minutes. Subsequently, this emulsion was passed through a homogenizer twice under a pressure of 150 kg/cm 2 to form a fine oil-in-water emulsion with a particle size of 1 to 3 μm. Store this emulsion in a container at 20℃.
It was left to cool until On the other hand, the outermost phase was dissolved at about 70℃, and this was dissolved at 40℃.
After being cooled to a temperature of approximately 20°C, it was rapidly cooled and plasticized using a votator. The oil-in-water emulsion was added to the obtained outermost phase at a ratio of 4:6 at 20° C. with stirring, and the mixture was stirred until no syneresis was observed. The production rate of the resulting oil-in-water type double emulsified fat composition was 69%.
It was hot. In addition, in order to see how easily the emulsification breaks down at the temperature in the mouth, the obtained fat and oil was heated to 37°C.
Quickly transfer to a centrifuge tube with a 300 c.c. scale and spin at 1000 rpm.
When centrifugation was performed for 10 minutes and the state of separation was observed, 76% of the total was separated into the outermost phase fat and oil and the inner phase oil-in-water emulsion. When I sampled this oil-in-water emulsified fat composition, it had a milky taste even though it did not contain any dairy products. Example 2 An oil-in-water-type double emulsified fat composition was obtained using the following formulation and the same operation as in Example 1.
二重乳化油脂組成物を作る際に、最内相油脂に
一定量のアンナツトカラーを加え、最外相油脂に
は着色剤を加えないでおく。出来た二重乳化油脂
組成物を100〜200g取り出し、約1.5cmの大きさ
に切り刻み、これを45℃に調整された水10の入
つた容器に投入し、撹拌機を用いて5分間ゆつく
りと撹拌する。尚、乳化の強さによつては5分間
では分離しないものも考えられるがその場合はさ
らに撹拌を続ければ良い。
一定時間撹拌後、撹拌機を止めると液面には最
外相油脂が浮き、他の大部分は白濁した水相部
(水中油型乳化物)とに分かれる。液面に浮いた
油脂を水相部が混入しない様注意深くピペツトで
すい取る。採取する量としては5〜10gで十分で
ある。さらに採取した油脂をろ紙でろ過し吸光度
測定の試料とする。
吸光度測定の条件としては光路長10mmのセルを
使用し波長420mμにて吸光度を測定する。また試
料温度は50℃で行なう。零合わせ及び100T合わ
せは二重乳化油脂組成物作成時に用いた最外相油
脂で行なう必要がある。
一方、二重乳化油脂組成物作成時に使用した最
外相及び最内相の油脂を種々の割合で混合し吸光
度を測定しこれを生成率の検量線として使用す
る。
さらに45℃の水中で撹拌中に最内相油脂が分離
し、最外相油脂とが合一してしまうことも考えら
れる為、測定精度を確認する意味で、最外相油脂
と中間及び最内相の水中油型乳化物を別々に45℃
の水中に投じ、5分間撹拌し、以下同様の操作を
ほどこし、測定操作中に低下した生成率を求めた
ところ実施例1及び2においてそれぞれ1.0%、
0.7%であつた。
When making a double emulsified fat composition, a certain amount of an uncut color is added to the innermost phase fat, and no coloring agent is added to the outermost phase fat. Take out 100 to 200 g of the double emulsified fat composition, cut it into pieces of about 1.5 cm, put it into a container containing 10 g of water adjusted to 45°C, and stir it slowly for 5 minutes using a stirrer. and stir. Depending on the strength of the emulsification, it is possible that the mixture may not separate within 5 minutes, but in that case, stirring may be continued. After stirring for a certain period of time, when the stirrer is stopped, the outermost phase of fat and oil floats on the liquid surface, and most of the other phase is separated into a cloudy aqueous phase (oil-in-water emulsion). Carefully pipette the fat floating on the liquid surface to avoid mixing it with the aqueous phase. It is sufficient to collect 5 to 10 g. Furthermore, the collected fats and oils are filtered through filter paper and used as a sample for absorbance measurement. The conditions for absorbance measurement are to use a cell with an optical path length of 10 mm and to measure absorbance at a wavelength of 420 mμ. Also, the sample temperature is 50°C. Zero adjustment and 100T adjustment must be performed using the outermost phase oil used when creating the double emulsified oil and fat composition. On the other hand, the outermost and innermost phase fats and oils used in preparing the double emulsified fat composition are mixed in various proportions, the absorbance is measured, and this is used as a calibration curve for the production rate. Furthermore, it is possible that the innermost phase oil and fat may separate during stirring in water at 45°C, and the outermost phase oil and fat may coalesce. Separate oil-in-water emulsions at 45°C.
of water and stirred for 5 minutes, and the same operation was performed thereafter to determine the production rate that decreased during the measurement operation. In Examples 1 and 2, it was 1.0%, respectively.
It was 0.7%.
Claims (1)
インナトリウム及び水溶性レシチンを含有し、且
つ外相油脂中にソルビタントリ脂肪酸エステルを
含有してなる油中水中油型二重乳化油脂組成物。 2 カゼインナトリウムの含有量が水中油型乳化
物に対して1.5〜5.0重量%である特許請求の範囲
第1項記載の組成物。 3 水溶性レシチンの含有量がカゼインナトリウ
ム100重量部に対して3〜15重量部である特許請
求の範囲第1項記載の組成物。 4 ソルビタントリ脂肪酸エステルの含有量が二
重乳化油脂組成物に対して0.1〜2.0重量%である
特許請求の範囲第1項記載の組成物。 5 内相としての水中油型乳化物と外相としての
油脂とからなる油中水中油型二重乳化油脂組成物
を製造するに際し、水相中にカゼインナトリウム
及び水溶性レシチンを添加して得られた水中油型
乳化物と、ソルビタントリ脂肪酸エステルを添加
した油脂とを混合乳化することを特徴とする油中
水中油型二重乳化油脂組成物の製造方法。 6 水中油型乳化物と油脂とを15〜25℃の範囲で
混合する特許請求の範囲第5項記載の製造方法。 7 カゼインナトリウムを水中油型乳化物に対し
て1.5〜5.0重量%添加する特許請求の範囲第5項
記載の製造方法。 8 水溶性レシチンをカゼインナトリウム100重
量部に対して3〜15重量部添加する特許請求の範
囲第5項記載の製造方法。 9 ソルビタントリ脂肪酸エステルを二重乳化油
脂組成物に対して0.1〜2.0重量%添加する特許請
求の範囲第5項記載の製造方法。[Claims] 1. An oil-in-water emulsion containing sodium caseinate and water-soluble lecithin in the aqueous phase of an oil-in-water emulsion as the internal phase, and a sorbitan trifatty acid ester in the external fat/oil phase. Double emulsified oil and fat composition. 2. The composition according to claim 1, wherein the content of sodium caseinate is 1.5 to 5.0% by weight based on the oil-in-water emulsion. 3. The composition according to claim 1, wherein the content of water-soluble lecithin is 3 to 15 parts by weight per 100 parts by weight of sodium caseinate. 4. The composition according to claim 1, wherein the content of sorbitan trifatty acid ester is 0.1 to 2.0% by weight based on the double emulsified oil and fat composition. 5. When producing an oil-in-water type double emulsified fat composition consisting of an oil-in-water emulsion as an internal phase and an oil or fat as an external phase, sodium caseinate and water-soluble lecithin are added to the aqueous phase. A method for producing an oil-in-oil-in-water double emulsified fat composition, which comprises mixing and emulsifying an oil-in-water emulsion containing a sorbitan trifatty acid ester and an oil-in-water emulsion containing a sorbitan trifatty acid ester. 6. The manufacturing method according to claim 5, wherein the oil-in-water emulsion and the oil or fat are mixed at a temperature of 15 to 25°C. 7. The manufacturing method according to claim 5, wherein 1.5 to 5.0% by weight of sodium caseinate is added to the oil-in-water emulsion. 8. The manufacturing method according to claim 5, wherein 3 to 15 parts by weight of water-soluble lecithin is added to 100 parts by weight of sodium caseinate. 9. The manufacturing method according to claim 5, wherein 0.1 to 2.0% by weight of sorbitan trifatty acid ester is added to the double emulsified oil/fat composition.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58086359A JPS59210971A (en) | 1983-05-16 | 1983-05-16 | Double-emulsified fatty oil composition and its preparation |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58086359A JPS59210971A (en) | 1983-05-16 | 1983-05-16 | Double-emulsified fatty oil composition and its preparation |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59210971A JPS59210971A (en) | 1984-11-29 |
| JPH0318669B2 true JPH0318669B2 (en) | 1991-03-13 |
Family
ID=13884689
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58086359A Granted JPS59210971A (en) | 1983-05-16 | 1983-05-16 | Double-emulsified fatty oil composition and its preparation |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59210971A (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59216628A (en) * | 1983-05-23 | 1984-12-06 | Kao Corp | Double emulsified oil and fat composition |
| JPS61185332A (en) * | 1985-02-12 | 1986-08-19 | Morinaga Milk Ind Co Ltd | Stable water in oil type emulsion and its preparation |
| JP3186189B2 (en) * | 1992-04-03 | 2001-07-11 | 日本ペイント株式会社 | Surface treatment agent for metal cans, method of using the same, and concentrated liquid for metal can surface treatment |
| JPH06220472A (en) * | 1993-01-29 | 1994-08-09 | Nippon Paint Co Ltd | Surface treatment for metallic can |
-
1983
- 1983-05-16 JP JP58086359A patent/JPS59210971A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59210971A (en) | 1984-11-29 |
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