JPH0648963B2 - Method for producing foamable oil-in-water emulsion composition - Google Patents

Method for producing foamable oil-in-water emulsion composition

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Publication number
JPH0648963B2
JPH0648963B2 JP60050198A JP5019885A JPH0648963B2 JP H0648963 B2 JPH0648963 B2 JP H0648963B2 JP 60050198 A JP60050198 A JP 60050198A JP 5019885 A JP5019885 A JP 5019885A JP H0648963 B2 JPH0648963 B2 JP H0648963B2
Authority
JP
Japan
Prior art keywords
oil
fatty acid
weight
acid ester
emulsifier
Prior art date
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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JP60050198A
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Japanese (ja)
Other versions
JPS61209562A (en
Inventor
貴志子 岡田
一三 葉山
行植 高
Original Assignee
アサヒフ−ズ株式会社
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Priority to JP60050198A priority Critical patent/JPH0648963B2/en
Publication of JPS61209562A publication Critical patent/JPS61209562A/en
Publication of JPH0648963B2 publication Critical patent/JPH0648963B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】 〔産業上の利用分野〕 この発明は食品分野における起泡性水中油型乳化組成物
の製造方法に関するものである。
TECHNICAL FIELD The present invention relates to a method for producing a foamable oil-in-water emulsion composition in the food field.

〔従来の技術〕[Conventional technology]

従来洋菓子類に広く用いられる生クリームは、風味およ
び口溶け(口当り)が非常に優れているが、価格面およ
び乳化安定性またはホイツプ時の保型性などの物性面で
は満足できるものではない。したがつて、このような生
クリームの欠点を解消するために、乳脂肪以外の動植物
性油脂を原料とした水中油型乳化組成物(以下、これを
合成クリームと略称する)が数多く開発され、大量に市
販されていることは周知のとおりである。
The fresh cream which has been widely used for Western confectionery has excellent flavor and melting in the mouth (mouthfeel), but it is not satisfactory in terms of price and physical properties such as emulsion stability or shape retention at whipping. Therefore, in order to eliminate the drawbacks of such a fresh cream, a large number of oil-in-water emulsion compositions (hereinafter, abbreviated as synthetic cream) made from animal and vegetable fats and oils other than milk fat have been developed, It is well known that a large amount is commercially available.

これら合成クームに必要な性質には、風味、耐熱性
(気温、室温などによる品温の上昇に耐える性質)や耐
振性(輸送、運搬などの際の振動に耐える性質)、ホ
イツプ時の起泡性と組織の緻密性、造花物の保型性お
よびその経時的安定性、造花物を凍結および解凍した
ときの原状の保持性などが挙げられるが、中でもホイツ
プ時に適度の起泡性を発現させようとするときは、合成
クリームに対して使用時までの乳化安定性を高めておく
一方で、ホイツプ時にはクリーム中の脂肪を凝集させ部
分的に乳化状態を破壊させるという本質的に相反する性
質を与えなければならないというむずかしさがある。そ
こで、起泡性の合成クリームを製造する際に最も影響の
大きい乳化剤について各方面で検討され、たとえば特開
昭58−209947号公報、特開昭56−13136
0号公報などにはポリグリセリン脂肪酸エステルを単独
使用した例が、特開昭56−21552号公報、特開昭
58−201956号公報、特開昭58−149649
号公報などにはモノグリセリン脂肪酸エステル、ソルビ
タン脂肪酸エステル、シヨ糖脂肪酸エステル、大豆リン
脂質、プロピレングリコール脂肪酸エステル、ポリグリ
セリン脂肪酸エステルなどを単独使用または併用した例
が、特公昭47−24925号公報にはポリグリセリン
脂肪酸エステルとレシチン、ケフアリン、リポイノシト
ール等を含むリン脂体とを併用した例が、特開昭57−
146551号公報にはHLB値の低いジグリセリン脂肪
酸エステル、トリグリセリン脂肪酸エステル(グリセリ
ンの2分子または3分子の縮合体を主成分としたもの)
は有効であつてもモノグリセリン脂肪酸エステルやオク
タグリセリン脂肪酸エステルのようなポリグリセリン脂
肪酸エステルは実用性がないという例が、さらに特開昭
58−111639号公報にはポリグリセリン脂肪酸エ
ステルと、炭素数12以上からなる一価有機酸(たとえ
ば、ラウリン酸、パルミチン酸、ステアリン酸、リノー
ル酸、リノレン酸等)と炭素数7以下からなる多価有機
酸(たとえば、クエン酸、コハク酸、酒石酸、リンゴ
酸、マレイン酸、アジピン酸等)またはそれのアセチル
誘導体とのデイグリセライド(1分子のグリセリンに1
分子の前記一価有機酸と1分子の前記多価有機酸または
それのアセチル誘導体がそれぞれエステル結合したも
の)を用いた例がそれぞれ記載されている。
Properties required for these synthetic combs include flavor, heat resistance (property to withstand increase in product temperature due to temperature, room temperature, etc.), vibration resistance (property to withstand vibration during transportation, transportation, etc.), whipping during whipping. Properties and tissue compactness, shape retention of artificial flower and its stability over time, retention of original state when frozen and thawed artificial flower, etc., but among them, appropriate foaming property is expressed at whipping. When this is done, the emulsion stability of the synthetic cream is increased until the time of use, while at the time of whipping, the fat in the cream is aggregated to partially destroy the emulsified state. There is a difficulty in giving it. Therefore, the emulsifier which has the greatest influence in the production of the foamable synthetic cream has been studied in various fields, for example, JP-A-58-209947 and JP-A-56-13136.
Examples of single use of polyglycerin fatty acid ester are disclosed in JP-A-56-21552, JP-A-58-201956 and JP-A-58-149649.
Examples of monoglycerin fatty acid ester, sorbitan fatty acid ester, sucrose fatty acid ester, soybean phospholipid, propylene glycol fatty acid ester, polyglycerin fatty acid ester and the like are used alone or in combination in Japanese Patent Publication No. 47-24925. Japanese Patent Application Laid-open No. 57-57-57 is a combination of polyglycerin fatty acid ester and phospholipids containing lecithin, kephalin, lipoinositol and the like.
JP-A-146551 discloses diglycerin fatty acid ester and triglycerin fatty acid ester having a low HLB value (based on a condensate of 2 or 3 molecules of glycerin as a main component).
Is effective, but polyglycerin fatty acid esters such as monoglycerin fatty acid ester and octaglycerin fatty acid ester are not practical. Further, JP-A-58-111639 discloses polyglycerin fatty acid ester and carbon number. Monovalent organic acids consisting of 12 or more (for example, lauric acid, palmitic acid, stearic acid, linoleic acid, linolenic acid, etc.) and polyvalent organic acids consisting of 7 or less carbon atoms (for example, citric acid, succinic acid, tartaric acid, apple) Acid, maleic acid, adipic acid, etc.) or its acetyl derivative with deglyceride (1 for 1 molecule of glycerin)
Examples of the monovalent organic acid and one molecule of the polyvalent organic acid or an acetyl derivative thereof are each ester-bonded.

しかし、昨今の製菓、製パン等の業界では、前記〜
の具備すべき諸条件のうち、特にホイツプ温度を通常の
4〜5℃または7〜8℃以下から15〜18℃以下と大
幅に上昇してもなお良好な起泡性を示し、長期間安定で
ある無菌クリームが要望されているが、無菌クリームの
製造工程における超高温滅菌(UHT、120〜150
℃、10〜2秒)では、クリーム中のタン白質の変性が
起こり、ホイツプ時間の短縮に伴つてオーバーランが低
く、得られる造花物の組織は粗く、離水しやすいなどの
多くの欠点が生じる。また、生産者、消費者の趣向の多
様化に伴つて、たとえばイチゴ、オレンンジ等の果汁も
しくは果実ソース、さらにはヨーグルトのような乳酸菌
発酵製品などを含む酸味のあるクリームに対しても強い
要望があるが、酸を加えると従来のクリームではタン白
質の凝集のほか、乳化剤の効力低下が促進され、その結
果、超高温滅菌処理したものは起泡性はなく、たとえ起
泡性があつても、造花物の組織は悪く、口当りも悪く、
前記の条件およびも満たされない。
However, in the recent confectionery and bread making industries,
Among the various conditions that must be met, even if the whip temperature is significantly increased from the usual 4 to 5 ° C or 7 to 8 ° C or less to 15 to 18 ° C or less, good whipping property is exhibited and stable for a long period of time. Aseptic cream is required, but ultra high temperature sterilization (UHT, 120-150) in the process of producing aseptic cream.
(° C, 10 to 2 seconds), the protein in the cream is denatured, the overrun is low with the shortening of the whipping time, and the texture of the resulting artificial flower is rough and many defects such as easy water release occur. . In addition, with the diversification of tastes of producers and consumers, there is a strong demand for sour creams containing fruit juices or fruit sauces such as strawberries and oranges, and lactic acid bacteria fermented products such as yogurt. However, addition of acid promotes aggregation of protein in conventional creams and reduction of potency of emulsifiers.As a result, those treated with ultra-high temperature sterilization do not have foaming properties, even if they have foaming properties. , The texture of the artificial flower is bad, the mouth feel is also bad,
The above conditions and also are not met.

〔発明が解決しようとする問題点〕[Problems to be solved by the invention]

したがつて、この発明は、風味、耐熱性、耐振性、起泡
性、組織の緻密性、保型性、経時的安定性、解凍後の原
状保持性が特に超高温滅菌処理またま酸味料添加などに
よつて満たされなくなるという従来の合成クリームの問
題点を解決しようとするものである。
Therefore, the present invention is particularly excellent in flavor, heat resistance, vibration resistance, foaming property, tissue compactness, shape retention, stability over time, original state retention after thawing, and ultrahigh temperature sterilization treatment or acidulant. It is intended to solve the problem of the conventional synthetic cream that it is not satisfied due to addition or the like.

〔問題点を解決するための手段〕[Means for solving problems]

上記の問題点を解決するために、この発明は組成重量百
分率で油脂25〜55%、タン白質0.5〜6.0%および乳
化剤を混合して水中油型(O/W型)乳化組成物を製造す
るに当り、乳化剤としてポリグリセリン脂肪酸エステル
0.05〜1.0%、レシチン0.05〜0.50%およびジアセチル
酒石酸モノグリセリド0.05〜0.50%を使用し、かつレシ
チンの配合量がポリグリセリン脂肪酸エステルとジアセ
チル酒石酸モノグリセリドとの合計量より少なくなるよ
うに配合し、さらにPH4.0以上となるように調整し
て、得られた水中油型乳化脂を超高温加熱滅菌処理する
手段を採用したのである。以下その詳細を述べる。
In order to solve the above problems, the present invention prepares an oil-in-water type (O / W type) emulsion composition by mixing 25 to 55% of oil and fat, 0.5 to 6.0% of protein and an emulsifier in composition weight percentage. Polyglycerin fatty acid ester as an emulsifier
0.05 to 1.0%, lecithin 0.05 to 0.50% and diacetyl tartaric acid monoglyceride 0.05 to 0.50% are used, and the content of lecithin is less than the total amount of polyglycerin fatty acid ester and diacetyl tartaric acid monoglyceride. It was adjusted to be not less than 0.0, and a means for sterilizing the obtained oil-in-water emulsified fat with ultrahigh temperature heat sterilization was adopted. The details will be described below.

まず、この発明における油脂は、たとえば牛脂、ラー
ド、バター、魚油などの動物性油脂、大豆油、ナタネ
油、綿実油、トウモロコシ油、パーム油、パーム核油、
ヤシ油などの植物性油脂、これら動植物性油脂に分別、
水素添加、エステル変換等の物理的、化学的手段を施し
た加工油脂などの単一種類または2種類以上の混合油脂
のいずれでもよく食用に供し得るものであればよい。そ
してこれら油脂類は上昇融点が30〜42℃、固体脂指
数(SFI)値が10℃で20〜50、15℃で15〜4
5、20℃で10〜40、25℃で5〜30、30℃で
0〜20の範囲のものが好ましく、融点、SFI値がこれ
らの値未満のものではホイツプクリームの稠度および保
型性の不充分となり、また逆にこれらの値を越える値の
ものでは、稠度、保型性が良好であつても増粘傾向が生
じ、特に風味および口当りが著しく損われるので好まし
くない。
First, the fats and oils in the present invention include beef tallow, lard, butter, animal fats and oils such as fish oil, soybean oil, rapeseed oil, cottonseed oil, corn oil, palm oil, palm kernel oil,
Vegetable oils and fats such as coconut oil, fractionated into these animal and vegetable oils and fats,
Any of a single type of fats and oils, such as processed fats and oils subjected to physical and chemical means such as hydrogenation and ester conversion, or a mixed fat or oil of two or more types may be used as long as it can be edible. These oils and fats have a rising melting point of 30 to 42 ° C, a solid fat index (SFI) value of 20 to 50 at 10 ° C, and 15 to 4 at 15 ° C.
5, the range of 10 to 40 at 20 ° C, the range of 5 to 30 at 25 ° C, and the range of 0 to 20 at 30 ° C are preferable. If the melting point and the SFI value are less than these values, the consistency and shape retention of the whipped cream are unsatisfactory. On the contrary, when the value exceeds these values, on the other hand, the viscosity and the shape-retaining property are good, but the tendency of thickening occurs, and the flavor and mouthfeel are remarkably impaired, which is not preferable.

つぎにこの発明のタン白質は主に牛乳、生クリーム、脱
脂粉乳、カゼインソーダ、ホエーパウダー、ホエーチー
ズのような無脂乳固形分、卵白タン白質、大豆タン白質
などの単一種類または2種以上を混合したものである。
Next, the protein of the present invention is mainly a single type or two types of milk, fresh cream, skim milk powder, casein soda, whey powder, non-fat milk solids such as whey cheese, egg white protein and soy protein. It is a mixture of the above.

さらに、この発明における乳化剤の一つであるポリグリ
セリン脂肪酸エステルはグリセリンの4〜10分子を縮
合しエーテル結合させた多量体であるポリグリセリンと
炭素数が12〜22個の飽和脂肪酸とのモノエステル体
であり、また、乳化剤のもう一つの成分であるレシチン
はホスフアチジルコリン、ホスフアチジルエタノールア
ミン、ホスフアチジルイノシトールなどを主成分とする
もので、通常油分を30〜40%含むペースト状大豆レ
シチンが用いられるが、卵黄レシチン、もしくは油分を
除去した大豆レシチンであつてもこの発明に支障を来た
すものではない。また、この発明のジアセチル酒石酸モ
ノグリセリドも乳化作用を呈するものであり、モノグリ
セリン脂肪酸エステルにジアセチル酒石酸を結合させて
得られるが、通常広く用いられるクエン酸モノグリセリ
ド、コハク酸モノグリセリド、乳酸モノグリセリドのよ
うなジアセチル酒石酸モノグリセリド以外の有機酸モノ
グリセリドでは造花物の離水や保型性などの点で好まし
くない。
Further, the polyglycerin fatty acid ester which is one of the emulsifiers in the present invention is a monoester of polyglycerin which is a polymer obtained by condensing 4 to 10 molecules of glycerin to form an ether bond and a saturated fatty acid having 12 to 22 carbon atoms. Lecithin, which is the body and another component of the emulsifier, is mainly composed of phosphatidylcholine, phosphatidylethanolamine, phosphatidylinositol, etc., and is usually a paste containing 30 to 40% oil. Soybean lecithin is used, but egg yolk lecithin or soybean lecithin from which oil has been removed does not hinder the present invention. Further, the diacetyl tartaric acid monoglyceride of the present invention also exhibits an emulsifying action, and is obtained by binding diacetyl tartaric acid to a monoglycerin fatty acid ester. Organic acid monoglycerides other than tartaric acid monoglyceride are not preferable in terms of water separation and shape retention of the artificial flower.

ここで、この発明において、油脂25〜55%、タン白
質0.5〜6.0%、ポリグリセリン脂肪酸エステル0.05〜1.
0%、レシチン0.05〜0.50%およびジアセチル酒石酸モ
ノグリセリド0.05〜0.50%とする理由はつぎのとおりで
ある。すなわち、油脂が25%未満のときは乳化安定性
は良好であつても起泡した造花物の保型性が劣り、逆に
55%を越える多量ではクリームの粘度が高くなり、可
塑化しやすく、オーバーランが低く口当りの悪いものに
なりやすい。タン白質はクリームの風味および起泡性を
付与する役割を果たすうえからは少なくとも0.5%が望
ましいが、6.0%を越える多量にすることはクリームの
粘度を上昇させ可塑化の原因ともなりかえつて不利とな
る。ポリグリセリン脂肪酸エステルは0.05%未満のとき
起泡の際のオーバーランが低くなり、逆に1.0%を越え
ると得られた造花物はいわゆる戻り(軟化)現象を起こ
したり、ホイツプ性を失つたりして好ましいクリームに
はならない。レシチンはポリグリセリン脂肪酸エステル
とつぎに述べるジアセチル酒石酸モノグリセリドの合計
量よりも少ないことが肝要であり、もし合計量よりも多
量になるとホイツプ時のオーバーランが低くなり、風味
や口当りの点でよくない。ジアセチル酒石酸モノグリセ
リドはポリグリセリン脂肪酸エステル1重量部に対して
0.15〜1.0重量部とすることが都合よく、0.05%未満で
は保型性、造花物の離水の点で問題があり、0.50%を越
える多量ではホイツプ性を失つたり、造花物が戻り(軟
化)現象を起こして好ましくない。
Here, in the present invention, fats and oils 25 to 55%, proteins 0.5 to 6.0%, polyglycerin fatty acid ester 0.05 to 1.
The reasons for setting 0%, lecithin 0.05 to 0.50% and diacetyl tartaric acid monoglyceride 0.05 to 0.50% are as follows. That is, when the oil and fat content is less than 25%, the emulsion stability is good, but the shape retention of the foamed artificial flower is poor, and conversely, when the oil content is more than 55%, the viscosity of the cream becomes high and it tends to be plasticized. It has a low overrun and tends to have a bad mouthfeel. At least 0.5% is desirable for the protein to play a role of imparting the flavor and foaming property of the cream, but a large amount exceeding 6.0% may increase the viscosity of the cream and cause plasticization, which is disadvantageous. Becomes When the polyglycerin fatty acid ester is less than 0.05%, the overrun at the time of foaming becomes low. On the contrary, when it exceeds 1.0%, the artificial flower obtained has a so-called reversion (softening) phenomenon or loses the whipping property. Does not give a desirable cream. It is essential that lecithin be less than the total amount of polyglycerin fatty acid ester and diacetyl tartaric acid monoglyceride described below. If it is more than the total amount, overrun during whipping will be low, which is not good in flavor and mouthfeel. . Diacetyl tartaric acid monoglyceride is based on 1 part by weight of polyglycerin fatty acid ester.
Conveniently 0.15 to 1.0 parts by weight, if less than 0.05% there is a problem in shape retention and water release of artificial flowers, and if it exceeds 0.50%, whip properties are lost or artificial flowers return (soften). ) Undesirably causing a phenomenon.

このようなこの発明における必須成分のほかに、この発
明の効果を損わない範囲でほかの乳化剤を併用してもよ
い。また、水溶液のpH緩衝、クリームの粘度低下、エマ
ルジヨンの安定化等の目的でよく使用される各種リン酸
塩が0.05〜0.50%の範囲内で添加される。さらに、各種
加工デンプン、ローカストビーンガム、グアーガム、カ
ラギーナン等の天然多糖類または酸性状態でタン白の凝
集を防止するためによく使用されるペクチン、カルボキ
シメチルセルロース(CMC)、メチルセルロース等の耐
酸性安定剤が0.01〜1.0%の範囲内で加えられる。また
シヨ糖、ブドウ糖、果糖、水あめ等の甘味料を適宜加え
て甘味の調整を行なつてもよい。
In addition to the essential components in this invention, other emulsifiers may be used in combination as long as the effects of the invention are not impaired. Further, various phosphates often used for the purpose of pH buffering of aqueous solution, reduction of viscosity of cream, stabilization of emulsion and the like are added within the range of 0.05 to 0.50%. In addition, natural polysaccharides such as modified starch, locust bean gum, guar gum, and carrageenan, or pectin, carboxymethylcellulose (CMC), methylcellulose, and other acid-resistant stabilizers that are often used to prevent protein aggregation under acidic conditions. Is added within the range of 0.01-1.0%. In addition, sweetness may be adjusted by appropriately adding sweeteners such as sucrose, glucose, fructose and starch syrup.

以上述べたこの発明の組成物の製造工程は特に限定され
るものではなく、通常広く実施されている工程と同じで
よい。すなわち、ポリグリセリン脂肪酸エステルなどの
親水性乳化剤は、通常水相に加えられるが、油脂中に分
散させてもよく、そのためにはたとえば70〜75℃の
加温した油脂中にポリグリセリン脂肪酸エステル、レシ
チン、ジアセチル酒石酸モノグリセリドの所定量を溶解
分散させ、別途70〜75℃に加温したタン白質源、リ
ン酸塩、安定剤等の水溶液を加えて撹拌し、一次乳化液
を調製する。ついでこの液を通常の場合20〜200kg
/cm2の圧力で均質機に通して均質化し、これに超高温滅
菌処理をを施せばこの発明の期待する起泡性水中油型乳
化組成物が得られる。ここで超高温滅菌処理は言うまで
もなく間接加熱、直接加熱のいずれの方式によるもので
あつてもよく、通常の場合、品温120〜150℃、処
理時間10〜2秒を一つの目安として行なえばよい。な
お、このような超高温滅菌処理後、さらに0〜200kg
/cm2にて再度均質化し、5℃前後に冷却し、一夜程度放
置して無菌包装機等を用いて包装し最終製品とすれば望
ましい起泡性水中油型乳化組成物が得られる。
The manufacturing process of the composition of the present invention described above is not particularly limited, and may be the same as the widely practiced process. That is, a hydrophilic emulsifier such as polyglycerin fatty acid ester is usually added to the aqueous phase, but it may be dispersed in oil or fat. For that purpose, for example, polyglycerin fatty acid ester in oil or fat heated at 70 to 75 ° C., A predetermined amount of lecithin and diacetyl tartaric acid monoglyceride is dissolved and dispersed, and an aqueous solution of protein source, phosphate, stabilizer and the like separately heated at 70 to 75 ° C. is added and stirred to prepare a primary emulsion. Then this solution is usually 20-200kg
The mixture is homogenized at a pressure of / cm 2 through a homogenizer and subjected to ultra-high temperature sterilization treatment to obtain the foamable oil-in-water emulsion composition expected of the present invention. Needless to say, the ultra-high temperature sterilization treatment may be performed by either indirect heating or direct heating. Normally, if the temperature of the product is 120 to 150 ° C. and the treatment time is 10 to 2 seconds, it may be used as a guideline. Good. In addition, after such ultra-high temperature sterilization, 0-200kg
The desired foamable oil-in-water emulsion composition can be obtained by homogenizing again at / cm 2 and cooling to about 5 ° C., leaving it to stand overnight, and packaging using an aseptic packaging machine to obtain the final product.

〔実施例〕〔Example〕

実施例および比較例における各試験項目およびその測定
方法はつぎのとおりである。すなわち、 (1)粘度:B型粘度計による5℃の粘度(センチポイズc
p) (2)最適起泡時間:電動ホイツパー(愛工舎製作所製Ken
mix)で500mlのクリーム状組成物を起泡させたとき
の最適起泡状態に達するまでの時間 (3)オーバーラン:次式によつて求めた最適起泡状態に
達したときの増加体積割合(%) (4)保型性:良好A、やや良好B、悪い(実用的でな
い)Cの3段階評価 (5)経時的保型性:25℃で24時間放置後の保型性 (6)組織:造花物の組織(きめ)について良好◎、やや
良〇、悪い(実用的でない)×の3段階評価 (7)離水:25℃で24時間放置後の造花物からの水の
分離の程度について、なし−、ほとんどなし±、ややあ
り+、多い++の4段階評価 (8)凍結解凍後の起泡クリームの物性:最適起泡状態の
クリーム−20℃で凍結し、そのまま1週間保存した後
5℃の冷蔵庫内で解凍して得られた起泡クリームに対す
る前記同様の保型性、組織および離水の評価 である。
The test items and their measuring methods in Examples and Comparative Examples are as follows. That is, (1) Viscosity: Viscosity at 5 ° C measured by a B-type viscometer (centipoise c
p) (2) Optimum foaming time: Electric whipper (Ken manufactured by Aikosha Seisakusho)
Mixing time until the optimum foaming state is reached when 500 ml of the creamy composition is foamed (3) Overrun: Increased volume ratio when the optimum foaming state is obtained by the following formula (%) (4) Shape retention: Three-level evaluation of good A, slightly good B, and bad (not practical) C (5) Temporal shape retention: Shape retention after standing at 25 ° C. for 24 hours (6) Structure: Three-level evaluation of good ◎, somewhat good ◯, poor (not practical) × for the texture of the artificial flower (7) Water separation: About the degree of separation of water from the artificial flower after leaving at 25 ° C for 24 hours, No-, Almost no ±, Somewhat +, Many ++ 4-level evaluation (8) Physical properties of foaming cream after freeze-thawing: cream in optimum foaming state-Frozen at -20 ° C and stored as it is for 1 week 5 It is the same shape retention, texture, and water separation evaluation for the foaming cream obtained by thawing in a refrigerator at ℃.

実施例1: 大豆硬化油(融点39℃)15重量部、パーム油(融点
39℃)8重量部、ヤシ硬化油(融点36℃)8重量
部、バター9重量部を70〜75℃に加温し、ヘキサグ
リセリンモノステアレート(阪本薬品工業社製:MS-50
0)0.16重量部、大豆レシチン0.12重量部、ジアセチル
酒石酸モノグリセリド(理研ビタミン社製:W−10)
0.1重量部を加え撹拌して均一に溶解分散させた。ま
た、脱脂粉乳4重量部、第二リン酸カリ0.03重量部、ヘ
キサメタリン酸ソーダ0.08重量部、シヨ糖12重量部、
コーンスターチ0.7重量部を水42.81重量部に溶解し、7
0〜75℃に加温した後、前記油相と混合し、70〜7
5℃に保持しながら30分間撹拌して一次乳化液とし
た。この液を40kg/cm2の均質化圧力で均質機に送り、
ついで超高温滅菌装置(岩井機械工業社製)によつて1
45℃、4秒間の直接加熱方式による滅菌処理を行なつ
た後10kg/cm2の均質化圧力で再度均質化して、直ちに
約5℃に冷却した。一夜放置した後無菌の起泡性水中油
型乳化組成物を得た。このものは風味がよく、表に示す
ように優れた物性を有し、起泡時の温度を通常の5〜7
℃以下から15〜18℃以下に大幅に拡張しても表に示
した物性とほぼ同等のものであり、この乳化組成物を5
℃前後で無菌の条件下に3カ月保存した後も、 油分離、凝集現象等は起こらず、風味および表に示した
各物性値も変化は認められなかつた。
Example 1: 15 parts by weight of hydrogenated soybean oil (melting point 39 ° C.), 8 parts by weight of palm oil (melting point 39 ° C.), 8 parts by weight of hardened coconut oil (melting point 36 ° C.), and 9 parts by weight of butter were added to 70 to 75 ° C. Heat and heat hexaglycerin monostearate (MS-50 manufactured by Sakamoto Yakuhin Kogyo Co., Ltd.)
0) 0.16 parts by weight, soybean lecithin 0.12 parts by weight, diacetyltartaric acid monoglyceride (manufactured by Riken Vitamin Co .: W-10)
0.1 part by weight was added and stirred to uniformly dissolve and disperse. Further, 4 parts by weight of skim milk powder, 0.03 parts by weight of potassium diphosphate, 0.08 parts by weight of sodium hexametaphosphate, 12 parts by weight of sucrose,
Dissolve 0.7 parts by weight of corn starch in 42.81 parts by weight of water,
After heating to 0 to 75 ° C., mixing with the oil phase, 70 to 7
While maintaining the temperature at 5 ° C, the mixture was stirred for 30 minutes to obtain a primary emulsion. This liquid is sent to a homogenizer at a homogenizing pressure of 40 kg / cm 2 ,
Then, using an ultra-high temperature sterilizer (made by Iwai Machinery Co., Ltd.) 1
After sterilization by direct heating at 45 ° C. for 4 seconds, the mixture was homogenized again at a homogenizing pressure of 10 kg / cm 2 and immediately cooled to about 5 ° C. After standing overnight, a sterile foamable oil-in-water emulsion composition was obtained. This product has a good taste and has excellent physical properties as shown in the table, and the temperature at the time of foaming is usually 5 to 7
The physical properties shown in the table are almost the same even if the temperature is greatly expanded from below 15 ° C to below 15-18 ° C.
Even after storing under aseptic conditions at around ℃ for 3 months, No oil separation, aggregation phenomenon, etc. occurred, and neither the flavor nor the physical properties shown in the table were observed.

実施例2: ヘキサグリセリンモノステアレートの代わりに、オクタ
グリセリンモノステアレート(ダルキ−・インダストリ
アル・フーズ社製:Santone 8-1-S)0.16重量部を用い
た以外は実施例1と全く同じ配合および方法によつて乳
化組成物を得た。このものは風味も優れ、表に示したと
おりの良好な物性をもつたものであつた。
Example 2: The same composition as in Example 1 except that 0.16 parts by weight of octaglycerin monostearate (Dalky Industrial Foods: Santone 8-1-S) was used in place of hexaglycerin monostearate. And an emulsified composition was obtained by the method. This product had an excellent flavor and had good physical properties as shown in the table.

比較例1 乳化剤の組成を大豆レシチン0.3重量部、ヘキサグリセ
リンモノステアレート(実施例1と同一品)0.15重量
部、ジアセチル酒石酸モノグリセリド(実施例1と同一
品)0.1重量部とし、大豆レシチンの使用量をポリグ
リセリン脂肪酸エステルとジアセチル酒石酸モノグリセ
リドの合計量より多くしたこと以外は実施例1と全く同
様の配合および方法で乳化組成物を得た。このものは表
に示したとおり起泡時間が長く、オーバーランも低く実
用的なものではなかつた。
Comparative Example 1 The composition of the emulsifier was 0.3 part by weight of soybean lecithin, 0.15 part by weight of hexaglycerin monostearate (the same product as in Example 1), and 0.1 part by weight of diacetyltartaric acid monoglyceride (the same product as in Example 1). An emulsified composition was obtained by the completely same formulation and method as in Example 1, except that the amount of was used was larger than the total amount of polyglycerin fatty acid ester and diacetyl tartaric acid monoglyceride. As shown in the table, this product had a long foaming time, had a low overrun, and was not practical.

比較例2 ジアセチル酒石酸モノグリドの代わりに、コハク酸モノ
グリセリド(イーストマン・ケミカル・プロダクツ社
製:Myverol SMG-V)0.1重量部を使用した以外は実施例
1と全く同じ配合および方法で乳化組成物を得た。この
ものは起泡時間が長く、離水も激しいため実用的なもの
ではなく、また、クエン酸モノグリセリド、乳酸モノグ
リセリドをジアセチル酒石酸の代わりに用いたときは、
起泡時間は幾分短縮されたが、離水および保型性の点で
は劣つていて、実用できるものではなかつた。
Comparative Example 2 An emulsified composition was prepared in exactly the same manner as in Example 1 except that 0.1 part by weight of succinic acid monoglyceride (Myverol SMG-V manufactured by Eastman Chemical Products Co., Ltd.) was used instead of diacetyl tartaric acid monoglide. Obtained. This product is not practical because it has a long foaming time and severe water separation, and when citric acid monoglyceride or lactic acid monoglyceride is used instead of diacetyl tartaric acid,
Although the foaming time was somewhat shortened, it was not practical because it was inferior in terms of water separation and shape retention.

比較例3: 乳化剤の組成をヘキサグリセリンモノステアレート(実
施例1と同一品)0.25重量部単独にした以外は実施例と
全く同様の配合および方法で乳化組成物を得た。このも
のは表に示したとおり、保型性が悪く、離水も激しいた
め実用的なものではなかつた。また、乳化剤の組成をヘ
キサグリセリンモノステアレート(実施例1と同一品)
0.15重量部とジアセチル酒石酸モノグリセリド(実施例
1と同一品)0.1重量部とし、レシチンを除いた乳化剤
を用いたときは、保型性、離水の点でレシチンを加えた
乳化剤のものに比べ劣つていた。
Comparative Example 3: An emulsified composition was obtained in exactly the same formulation and method as in Example except that the emulsifier composition was 0.25 parts by weight of hexaglycerin monostearate (the same product as in Example 1) alone. As shown in the table, this product was not practical because it had poor shape retention and severe water separation. In addition, the composition of the emulsifier was hexaglycerin monostearate (the same product as in Example 1).
When 0.15 parts by weight and 0.1 part by weight of diacetyl tartaric acid monoglyceride (the same product as in Example 1) were used and the emulsifier without lecithin was used, it was inferior to the one with lecithin added in terms of shape retention and water separation. Was there.

実施例3〜6: 実施例1と同じ原料の大豆硬化油15重量部、パーム油
5重量部、ヤシ硬化油10重量部を70〜75℃に加温
し、ヘキサグリセリンモノステアレート0.18重量部、大
豆レシチン0.14重量部、ジアセチル酒石酸モノグリセリ
ド0.12重量部を加えて撹拌し、溶解分散させた。一方、
脱脂粉乳4重量部、ストロベリーソース20重量部、シ
ヨ糖10重量部、第二リン酸カリ0.03重量部、ヘキサメ
タリン酸ソーダ0.08重量部、カルボキシメチルセルロー
ス(第一工業製薬製:セロゲンF−AG)0.08重量部を水
35.37重量部に溶解させた水相を70〜75℃に加温し
た後、前記の油相と混合し、70〜75℃に保持して3
0分間撹拌し、一次乳化液とした。この液を実施例1と
同じ条件で均質機および超高温滅菌装置に送り、さらに
再度均質化した後直ちに5℃前後に冷却した。一夜放置
した後pH5.69の無菌の起泡性水中油型乳化組成物(実施
例3)を得た。この乳化組成物は風味もよく、表に示し
たとおり良好な物性を有し、無菌条件下5℃で3カ月経
過後も油分離、凝集の現象は全く認められず、風味およ
び各物性にも変化はなかつた。なお、実施例3の乳化組
成物の調製過程において、クエン酸とリンゴ酸とを等量
混合した溶液を作り、この液を実施例3の一次乳化液の
調製時に添加し、pHを5.00(実施例4)、4.80(実施例
5)、4.50(実施例6)と順次低下させ、それぞれに実
施例3と同様の処理を施して乳化組成物を得た。表に示
したとおりpH4.50(実施例6)まで酸性になつた組成物
も起泡性クリームとして望ましい各物性を充分に保持し
ていた。
Examples 3 to 6: 15 parts by weight of soybean hydrogenated oil, 5 parts by weight of palm oil, and 10 parts by weight of hydrogenated coconut oil, which are the same raw materials as in Example 1, were heated to 70 to 75 ° C. and 0.18 parts by weight of hexaglycerin monostearate. Then, 0.14 parts by weight of soybean lecithin and 0.12 parts by weight of diacetyl tartaric acid monoglyceride were added and stirred to dissolve and disperse. on the other hand,
Non-fat dry milk 4 parts by weight, strawberry sauce 20 parts by weight, sucrose 10 parts by weight, potassium diphosphate 0.03 parts by weight, sodium hexametaphosphate 0.08 parts by weight, carboxymethyl cellulose (Daiichi Kogyo Seiyaku Co., Ltd .: serogen F-AG) 0.08 parts by weight Part of water
The aqueous phase dissolved in 35.37 parts by weight was heated to 70 to 75 ° C, then mixed with the above oil phase, and kept at 70 to 75 ° C for 3 times.
The mixture was stirred for 0 minutes to give a primary emulsion. This solution was sent to a homogenizer and an ultra-high temperature sterilizer under the same conditions as in Example 1, further homogenized again, and immediately thereafter cooled to around 5 ° C. After standing overnight, a sterile foamable oil-in-water emulsion composition (Example 3) having a pH of 5.69 was obtained. This emulsified composition had a good taste and had good physical properties as shown in the table, and even after 3 months at 5 ° C. under aseptic conditions, no oil separation or agglomeration phenomenon was observed, and the emulsified composition had neither taste nor physical properties. No change. In the process of preparing the emulsified composition of Example 3, a solution was prepared by mixing equal amounts of citric acid and malic acid, and this solution was added at the time of preparing the primary emulsion of Example 3 to adjust the pH to 5.00 (implementation). Example 4), 4.80 (Example 5), and 4.50 (Example 6) were sequentially decreased, and the same treatment as in Example 3 was applied to each to obtain an emulsified composition. As shown in the table, the composition that had been acidified to pH 4.50 (Example 6) also sufficiently retained each physical property desired as a foaming cream.

比較例4および5: 実施例6よりもクエン酸とンゴ酸との等量混合液をさら
に加えて、pHが3.8(比較例4)および3.0(比較例5)
の乳化組成物を実施例3〜6と同様の操作で滅菌処理お
よび再度均質化した後急冷し、5℃前後で一夜放置した
ところ、放置中に乳化組成物は分離現象を起こし、物性
は測定不能であつた。
Comparative Examples 4 and 5: A pH of 3.8 (Comparative Example 4) and 3.0 (Comparative Example 5) was obtained by further adding an equal volume mixture of citric acid and ngoic acid as compared with Example 6.
The emulsified composition of Example 1 was sterilized and homogenized again in the same manner as in Examples 3 to 6 and then rapidly cooled and allowed to stand overnight at about 5 ° C., and the emulsified composition caused a separation phenomenon during standing and the physical properties were measured. It was impossible.

〔効果〕〔effect〕

以上述べたように、この発明の乳化組成物は風味が良好
で長期にわたつて安定な無菌の合成クリームであり、ホ
イツプ温度が16〜19℃であつても起泡性は良好で作
業性が優れ、造花物の保型性、組織さらに凍結解凍に対
する耐性も良好であると同時に酸味料を加えて超高温滅
菌処理のような過酷な処理を施してもpH4.0まではクリ
ームの物性に何ら悪影響が現われないなどは、従来の合
成クリームには見られないことであり、この発明の意義
はきわめて大きいということができる。
As described above, the emulsified composition of the present invention is an aseptic synthetic cream having a good flavor and stable over a long period of time. Even when the whip temperature is 16 to 19 ° C, the foamability is good and the workability is high. It has excellent shape retention of the artificial flower, good texture and resistance to freezing and thawing. At the same time, even if it is subjected to severe treatment such as ultra-high temperature sterilization treatment with an acidulant, the physical properties of the cream are up to pH 4.0. The fact that no adverse effects appear is not found in conventional synthetic creams, and it can be said that the significance of the present invention is extremely great.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】組成重量百分率で油脂25〜55%、タン
白質0.5〜6.0%および乳化剤を混合乳化して起泡
性水中油型乳化組成物を製造するに当り、乳化剤として
ポリグリセリン脂肪酸エステル0.05〜1.0%、レ
シチン0.05〜0.50%およびジアセチル酒石酸モ
ノグリセリド0.05〜0.50%を使用し、かつレシ
チンの配合量がポリグリセリン脂肪酸エステルとジアセ
チル酒石酸モノグリセリドとの合計量より少なくなるよ
うに配合し、さらにPH4.0以上となるように調整し
て、得られた水中油型乳化脂を超高温加熱滅菌処理する
ことを特徴とする起泡性水中油型乳化組成物の製造方
法。
1. When a foamable oil-in-water emulsified composition is produced by mixing and emulsifying 25 to 55% of oils and fats, 0.5 to 6.0% of protein and an emulsifier in composition weight percentage, a poly emulsifier is used as an emulsifier. Glycerin fatty acid ester 0.05 to 1.0%, lecithin 0.05 to 0.50% and diacetyl tartaric acid monoglyceride 0.05 to 0.50% are used, and the amount of lecithin compounded is polyglycerin fatty acid ester and diacetyl tartaric acid. It is blended so as to be less than the total amount with monoglyceride, further adjusted to have a pH of 4.0 or more, and the obtained oil-in-water emulsified fat is subjected to ultra-high temperature heat sterilization treatment. A method for producing an oil-based emulsion composition.
【請求項2】ポリグリセリン脂肪酸エステルがグリセリ
ンの4〜10分子を縮合しエーテル結合させた多量体で
あるポリグリセリンと炭素数が12〜22個の飽和脂肪
酸とのモノエステル体である特許請求の範囲第(1)項記
載の起泡性水中油型乳化組成物の製造方法。
2. A polyglycerin fatty acid ester is a monoester of polyglycerin, which is a multimer of 4 to 10 molecules of glycerin condensed and ether-bonded, and a saturated fatty acid having 12 to 22 carbon atoms. A method for producing the foamable oil-in-water emulsion composition according to item (1).
JP60050198A 1985-03-11 1985-03-11 Method for producing foamable oil-in-water emulsion composition Expired - Lifetime JPH0648963B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60050198A JPH0648963B2 (en) 1985-03-11 1985-03-11 Method for producing foamable oil-in-water emulsion composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60050198A JPH0648963B2 (en) 1985-03-11 1985-03-11 Method for producing foamable oil-in-water emulsion composition

Publications (2)

Publication Number Publication Date
JPS61209562A JPS61209562A (en) 1986-09-17
JPH0648963B2 true JPH0648963B2 (en) 1994-06-29

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ID=12852436

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JPH0648963B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8712818D0 (en) * 1987-06-01 1987-07-08 Unilever Plc Artificial cream
JP2753730B2 (en) * 1989-05-23 1998-05-20 雪印乳業株式会社 Process for producing oil-in-water creamy composition having foaming properties
ATE198121T1 (en) * 1994-09-24 2001-01-15 Nestle Sa HEAT-Stable OIL-IN-WATER EMULSION AND METHOD FOR PRODUCING THE SAME
JP3118155B2 (en) * 1994-12-01 2000-12-18 アサヒフーズ株式会社 Whipping cream composition having low fat content, acid resistance and freezing resistance and method for producing the same
PT716811E (en) * 1994-12-13 2001-07-31 Produits Nestle S A Societe De HEAT-IN-WATER EMULSES CONTAINING HEAT CONTAINING EGG GEM AND PROCESS FOR THEIR PREPARATION
PT768042E (en) * 1995-10-13 2002-01-30 Nestle Sa PRODUCT TYPE MAIONE
JP4674961B2 (en) * 2000-12-08 2011-04-20 三菱化学株式会社 Oil-in-water emulsion
KR100913121B1 (en) 2007-08-14 2009-08-19 주식회사농심 The Food Emulsifier, the Preparation method of the Food Emulsifier, The Functional oil product with emulsifier and the preparation of the Functional oil product
JP2019195293A (en) * 2018-05-09 2019-11-14 ミヨシ油脂株式会社 Oil-in-water type emulsified material and whipped cream using same

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