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JPH0342866B2 - - Google Patents
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JPH0342866B2 - - Google Patents

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Publication number
JPH0342866B2
JPH0342866B2 JP58105677A JP10567783A JPH0342866B2 JP H0342866 B2 JPH0342866 B2 JP H0342866B2 JP 58105677 A JP58105677 A JP 58105677A JP 10567783 A JP10567783 A JP 10567783A JP H0342866 B2 JPH0342866 B2 JP H0342866B2
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Japan
Prior art keywords
emulsification
oil
water
product
phase
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JP58105677A
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Japanese (ja)
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JPS59232048A (en
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Priority to JP58105677A priority Critical patent/JPS59232048A/en
Publication of JPS59232048A publication Critical patent/JPS59232048A/en
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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は、食感が良好なマーガリン様の油中水
型乳化組成物の製造法に関するものである。 マーガリンは一般的に、溶融状態にある油相中
に水相を乳化して油中水型乳化(以下W/O乳化
と称する)の予備乳化液とし、さらにこれを急冷
〓和することにより製造される。マーガリンの乳
化状態は予備乳化液と同じくW/O乳化であり、
連続相をなす油相は、急冷〓和によりなめらかな
可塑性を有する固定状となり、液状の水相を分散
相として安定に乳化保持している。 一方バターの製造方法についてみると、一般的
にバターは生クリームの乳化状態を反転させるこ
とにより製造される。生クリームは水中油型乳化
(以下O/W乳化と称する)であり、水相中に固
体状の脂肪球が分散している。バターの製造時に
は生クリームを強く撹拌することによりこの脂肪
球同士を凝集させ粗大な脂肪粒を得る(この操作
をチヤーニングと称する)。この時水相の一部が
脂肪粒内部に取り込まれ、脂肪粒はW/O乳化と
なる。次いでこの脂肪粒を取り出して(余分の水
分は除去して)さらにこれを〓和することにより
W/O乳化のバターを得る。 上記のマーガリンとバターの製造方法の違いは
両者の食感に大きな差異を与えている。すなわち
マーガリンは連続相である油相がなめらかな可塑
性固体状で強固なW/O乳化状態にある為、口中
で油相がなめらかに広がり油脂によるワキシーな
食感を与える。また水相部は容易に舌に触れない
為、その呈味が不良である。これに対してバター
は製品の乳化状態はマーガリンと同じくW/O乳
化であるが、その連続相である油相は脂肪球同士
が凝集して形成されている為不均一な状態にあ
る。この為、マーガリンのように油脂が口中でな
めらかに広がらず、従つてマーガリンに比較して
ワキシーな食感が弱く、水相部も容易に舌に触れ
る為呈味が良好である。 そこで、バターと同じ製造方法をマーガリンに
適用することにより、バターと同等の食感を有す
るマーガリンを製造することが考えられている。 しかし、チヤーニング法は急冷〓和法に比較し
て得られたマーガリンの食感は良好であるが、工
程的にはかなり複雑である。また脂肪粒の取り出
しの段階で過剰の水分とともに水溶性の成分の一
部も失なわれる為原材料のロスも大きい。さらに
製造時の細菌汚染の危険も急冷〓和法より大きく
衛生管理ま難しい。この為、一部の高級マーガリ
ンの他はこの方法は用いられていないのが現状で
ある。 本発明者らは、通常の急冷〓和法と同様の簡単
の工程であつて、しかも食感の良好なマーガリン
が得られる製造方法の開発を目的としてこれまで
種々検討を行なつてきた。その結果、特定の乳化
剤および蛋白質を使用し油相と水相の比率を特定
の割合に保つことにより、予備乳化時安定なO/
W乳化状態となり、ついで急冷〓和装置内で冷却
され〓和(ワーキング)されることにより余剰の
水分が分離することなくW/O乳化に反転してマ
ーガリン様の均一な乳化組成物が得られ、しかも
この組成物が優れた食感を有することを見い出し
本発明を完成させた。 すなわち本発明は、HLB11以上のシヨ糖脂肪
酸エステルを組成物全量に対して0.2〜2.0重量
%、乳蛋白質および/または植物蛋白質を組成物
全量に対して0.2〜3.0重量%含有する水相部と、
完全に溶融状態にある油相部を、両者の容量比が
水相部/油相部=15/85〜45/55になる組成で水
中油型に予備乳化し、その予備乳化液を急冷〓和
することにより乳化状態をW/O乳化に反転させ
て、均質な可塑性を有する製品を得ることを特徴
とする、油中水型乳化組成物の製造法に関するも
のである。 本発明に使用するシヨ糖脂肪酸エステルはモノ
エステル主体でHLBが11以上のものであること
が必要である。その構成脂肪酸の種類としてはス
テアリン酸、パルミチン酸を主成分とするものが
好ましい。蛋白質は乳蛋白質および/または植物
蛋白質を使用する。乳蛋白質は一般には乳、濃縮
乳、粉乳、醗酵乳の形で加えるが、カゼインある
いはカゼインナトリウム等の製剤を使用すること
も可能である。植物蛋白質としては大豆蛋白質、
落花生蛋白質等を使用できる。 HLB11以上のシヨ糖脂肪酸エステルおよび蛋
白質は、予備乳化時に安定なO/W乳化を維持し
急冷〓和後の製品の食感を高める為に不可欠の成
分である。シヨ糖脂肪酸エステルの比率が0.2重
量%未満であるかあるいは蛋白質の比率が0.2重
量%未満の場合は、予備乳化時に安定なO/W乳
化とならず従つて食感の良好な製品は得られな
い。また逆にこれらの成分が過剰になると急冷〓
和時にW/O乳化への反転が良好に行なわれず製
品が分離状態となる。良好なW/O乳化への反転
を行なう為には、シヨ糖脂肪酸エステルの比率の
上限は2.0重量%、蛋白質の比率の上限は3.0重量
%である。さらに、シヨ糖脂肪酸エステルの
HLBもO/W乳化を維持し食感を高める為に重
要である。シヨ糖脂肪酸エステルのHLBが11よ
り低い場合は予備乳化時にO/W乳化が維持でき
ず、製品の食感が悪くなる。 予備乳化時O/W乳化を維持し急冷〓和時に
W/O乳化への反転を良好に行なう為には、油相
と水相の容量比も重量である。本発明において予
備乳化時に良好なO/W乳化状態を保つために
は、水相の容量比が少なくとも水相/油相=15/
85より大きいことが必要である。水相の容量比が
これより低い場合には乳化状態がW/O乳化に反
転するかあるいは不安定な状態になつたり、ある
いは予備乳化液が著しく増粘する。一方、O/W
乳化の予備乳化液を急冷〓和時に完全にW/O乳
化に反転させる為には水相の比率には上限があ
り、水相/油相=45/55を越えて水相の容量比が
高くなると、急冷〓和時に製品がW/O乳化に反
転しない。 本発明に用いる油脂は天然の動植物油脂および
それらの硬化油、分別油、エステル交換油等であ
り、これらを任意に配合して使用することができ
る。油脂の硬さとしては一般のバターあるいはマ
ーガリンと同様に融点40℃以下で、常温で10〜40
%の固体脂を有し可塑性を有するものが好まし
い。 乳化剤としてはシヨ糖脂肪酸エステル以外に必
要に応じてグリセリン脂肪酸エステル、レシチ
ン、ソルビタン脂肪酸エステル、プロピレングリ
コール脂肪酸エステル等を使用することができ
る。またその他の成分としては、甘味を有するス
プレツドあるいはバタークリーム用の製品等にお
いては糖質を添加することができる。また風味の
向上の為、卵等の呈味成分の使用あるいは着香
料、着色料の使用も自由に行なうことができる。 本発明の方法はO/W乳化の予備乳化液を急冷
〓和によりW/O乳化に反転して製品を得る。予
備乳化は水相中に撹拌しながら油相を少しずつ添
加して分散、乳化することにより行なう。油相を
加え終えた後も引き続き撹拌を続け油相の分離を
防ぎ乳化を安定化させる。撹拌機の種類はどのよ
うな形式のものでも可能であるが、高速回転の剪
断力の強い撹拌機の方が良好な乳化が達成され
る。通常の撹拌機により乳化を行なつた終、さら
に高圧均質機等により均質化を行ない粒径を小さ
くそろえることも可能である。予備乳化の際に油
相は完全に溶解した状態で水相に添加し、予備乳
化液は急冷〓和を行なうまで油相が結晶化しない
温度に保持することが必要である。 予備乳化後の急冷〓和は通常のマーガリンと同
様に、連続密閉式の急冷〓和装置を使用するのが
好ましい。マーガリン製造用の連続密閉式急冷〓
和装置は、現在国内外で様々な名称のものが発売
されているが、いずれも基本的な構造は同一であ
り、内面かき取り式熱交換機からなる冷却ユニツ
トとピンマシンによるワーキングユニツトを組み
合わせた構造である。本発明ではこの形式のマー
ガリン製造装置であればいずれも使用可能であ
り、一般のマーガリン製造設備をそのまま利用す
ることができる。 予備乳化液の急冷〓和にあたつては、乳化状態
をO/W乳化からW/O乳化に反転する為にまず
冷却ユニツトにより乳化液を充分冷却する必要が
ある。この時の冷却が弱いと油脂の結晶化が充分
に行なわれずその後の〓和によつても乳化の反転
が不充分となる。乳化を完全に反転させて均一な
W/O乳化の製品を得る為には、冷却ユニツト出
口での品温が、原料油脂のSFIが15である温度よ
り低いことが望ましい。 冷却ユニツトから出た予備乳化液はこの段階で
はまだO/W乳化であり、その後ワーキングユニ
ツトにより〓和されてW/O乳化に反転する。こ
の時の〓和を受ける時間が乳化状態に大きな影響
を与える。すなわち〓和される時間が短いと製品
は乳化の反転が充分に行なわれずに分離気味とな
り、逆に〓和される時間が長過ぎると乳化反転後
もさらに長時間のワーキングを受けることにより
製品が練られすぎて脂肪球が完全に破壊され本発
明の目的とする優れた食感の製品が得られない。
ワーキングユニツトでの〓和時間はその容量と製
品流量により決定される。分離のない均一な状態
であつてしかも良好な食感を有する製品を得る為
にはワーキングユニツトの容量/製品流量(すな
わち平均滞留時間)が60秒から180秒の範囲にな
るように製品流量を設定することが望ましい。 本発明により製造される製品は、通常の急冷〓
和法により製造されるマーガリンに比較して、呈
味が良好であり可塑性油脂特有のワキシーな食感
を感じない。またチヤーニング法により製造した
マーガリンあるいはバターと比較しても、本発明
の方法による製品は、むしろ両者より優れた食感
を有している。また、製造工程について比較して
も、本発明はチヤーニング法のような繁雑な操作
を必要とせず、チヤーニング法におけるO/W乳
化液の結晶化とチヤーニングおよび〓和に相当す
る工程を連続して密閉系で行なつており、余剰の
水分を系外に排除する必要もない。しかも設備的
には、既存のマーガリン製造設備を殆んど改変せ
ずに使用することが可能であり、工業的に有利で
ある。 本発明による製品は優れた食感を有し、パン等
にスプレツドあるいはサンドして使用するのに適
している。また本発明による製品は通常のマーガ
リンと同様にミキサー等でホイツプしてバターク
リームとして使用することも可能である。 本発明では油相部が容量で60%以上であれば良
好な製品が得られるので、一般のマーガリンある
いはバターに比較して低油分の製品を作ることが
可能であり、健康上からも通常のバター、マーガ
リンより有利である。 以下に本発明の実施例を示し、また比較実験例
により本発明の効果を詳述する。 実施例 1 下記配合により油中水型乳化組成物を製造し
た。 (油相部) ナタネ硬化油(融点37℃) 50Kg パーム油 35Kg 大豆油 15Kg モノグリセリド(ステアリン酸主体) 50g 大豆レシチン 100g バターフレーバー 30g (水相部) 水 55Kg 脱脂粉乳 5Kg シヨ糖脂肪酸エステル(HLB16、ステアリン酸
主成分) 1Kg 食 塩 2Kg この配合で水相部/油相部の容量比は35/65で
あつた。また乳化剤を含む油相部のSFIは15℃で
21.7であつた。 製法はまず各油脂を70℃以上に昇温して溶融
し、これらを混合した後モノグリセリド、大豆レ
シチンを添加して70℃以上で完全に溶解させた。
次いでこの油相を60〜65℃に冷却してバターフレ
ーバーを加えてこの温度に引き続き保持した。 一方これと併行して水に脱脂粉乳、シヨ糖脂肪
酸エステル、食塩を加え70℃に昇温して完全に溶
解させることにより水相を調製した。 次に水相を800rpmで回転するタービン状撹拌
羽根の撹拌機で撹拌しながら油相を除々に加え、
その後さらに30分以上60〜65℃に保持しながら撹
拌を続けることにより予備乳化を行なつた。これ
により得られる予備乳化液はO/W乳化であつ
た。 次いでこの予備乳化液を下記のコンビネーター
を用いて急冷〓和して目的とするW/O乳化の製
品を得た。このコンビネーターは2本の冷却ユニ
ツトおよび1本のワーキングユニツトからなる連
続密閉式の急冷〓和機である。このコンビネータ
ーの運転条件は製品流量70Kg/hrで、Aユニツト
出口での製品温度が5℃になるように冷媒温度を
調整した。この時のワーキングユニツトにおける
平均滞留時間は計算値で110秒間であつた。 以上の操作により得られた製品はマーガリンあ
るいはバターと同様の外観を有し、品温15〜25℃
で良好なスプレツド性を有していた。またその食
感は一般のマーガリンのようなワキシーな感じが
なく、塩味および乳の呈味が良好で極めて好まし
い食感であつた。 実施例 2 以下の配合で油中水型乳化組成物を製造した。 (油相部) 魚硬化油(融点32℃) 75Kg 大豆油 25Kg モノグリセリド(ステアリン酸、オレイン酸主
体、IV50のもの) 100g 大豆レシチン 100g バターフレーバー 30g (水相部) 水 60Kg 大豆蛋白質 1Kg シヨ糖脂肪酸エステル(HLB14、ステアリン酸
主体) 1Kg 砂 糖 30Kg ミルクフレーバー 200g この配合での水相/油相の容量比は42/58であ
つた。また油相のSFIは10℃で23.5であつた。 上記配合で、実施例1と全く同様に製造して得
られた製品は、実施例1による製品と同様に良好
な製品状態、食感を有し、甘味のあるスプレツド
として極めて好ましいものであつた。またこの製
品をホイツプして得られたバタークリームハ状態
が良好で、食感も通常のバタークリームに比較し
て非常に良好であつた。 実施例 3 以下の配合で油中水型乳化組成物を製造した。 (油相部) ナタネ硬化油(融点37℃) 40Kg バターオイル 40Kg コーン油 20Kg モノグリセリド(実施例1と同じ) 100g 大豆レシチン 100g バターフレーバー 20g (水相部) 水 70Kg 脱脂粉乳 3Kg カゼインナトリウム 1Kg シヨ糖脂肪酸エステル(HLB16、ステアリン酸
主体) 0.8Kg 食 塩 2Kg この配合で水相部/油相部の容量比は40/60で
あつた。また乳化剤を含む油相部のSFIは15℃で
24.5であつた。 製法はまず実施例1と同様に油相部および水相
部を調製し予備乳化を行なつた。次にこの予備乳
化液を高圧均質機を用いてM型均質バルブで圧力
50Kg/cm2で均質化した。次いでこの均質化液を実
施例1と同様にコンビネーターに通すことにより
油中水型乳化組成物を得た。 これにより得られた製品はバターに非常に良く
似た風味を有し、食感はバターより良好であつ
た。またスプレツド性もバターより良好であり、
スプレツド用の製品として極めて好ましいもので
あつた。 比較実験例 1 シヨ糖脂肪酸エステルの添加量を変えて実験番
号1〜5の乳化物を調製し一連の実験を行なつ
た。シヨ糖脂肪酸エステル以外の成分の配合はす
べて実施例1と同じである。またシヨ糖脂肪酸エ
ステルは実施例1と同じ種類のものを使用した。
製法も実施例1と同様に行なつた。表−1に各実
験におけるシヨ糖脂肪酸エステルの添加量および
実験結果を示す。これらのうち実験番号3は実施
例1に記載したものに相当する。 実験番号1は、シヨ糖脂肪酸エステルの比率が
本発明で必要とする量の下限値以下である。この
場合は表−1に示す様に予備乳化時O/W乳化が
維持できず従つて食感が不良である。逆にシヨ糖
脂肪酸エステルの比率が本発明の上限値を越える
実験番号5では急冷〓和によりW/O乳化の製品
が得られない。これに対し実験番号2、3、4は
シヨ糖脂肪酸エステルの比率が本発明の範囲内に
ある。比率が下限値に近い実験番号2ではやや予
備乳化状態が不安定であるが、食感には本発明の
効果が認められる。またこの比率が上限値に近い
実験番号4ではやや製品状態が不良であるが実用
可能な範囲にある。 以後、W/Oは油中水型乳化をO/Wは水中油
型乳化を示す。
The present invention relates to a method for producing a margarine-like water-in-oil emulsion composition with good texture. Margarine is generally manufactured by emulsifying an aqueous phase into a molten oil phase to create a pre-emulsification liquid for water-in-oil emulsification (hereinafter referred to as W/O emulsification), and then rapidly cooling and homogenizing this. be done. The emulsified state of margarine is a W/O emulsion, same as the pre-emulsified liquid,
The oil phase, which is a continuous phase, becomes a fixed state with smooth plasticity by rapid cooling and quenching, and the liquid water phase is stably emulsified and maintained as a dispersed phase. On the other hand, regarding the method for producing butter, butter is generally produced by reversing the emulsification state of fresh cream. Fresh cream is an oil-in-water emulsion (hereinafter referred to as O/W emulsion), and solid fat globules are dispersed in an aqueous phase. When making butter, fresh cream is strongly stirred to cause these fat globules to coagulate and form coarse fat particles (this operation is called churning). At this time, part of the aqueous phase is taken into the fat granules, and the fat granules become a W/O emulsion. Next, the fat granules are taken out (excess water is removed) and further summed to obtain W/O emulsified butter. The above-mentioned difference in the manufacturing method of margarine and butter gives a big difference in the texture of the two. In other words, the continuous oil phase of margarine is a smooth plastic solid and is in a strong W/O emulsion state, so the oil phase spreads smoothly in the mouth and gives the product a waxy texture due to the fats and oils. Furthermore, since the aqueous phase does not easily touch the tongue, the taste is poor. On the other hand, the emulsification state of butter is a W/O emulsion like margarine, but its continuous phase, the oil phase, is in a non-uniform state because it is formed by agglomeration of fat globules. For this reason, unlike margarine, fats and oils do not spread smoothly in the mouth, and therefore the texture is less waxy than margarine, and the aqueous phase easily touches the tongue, resulting in a good taste. Therefore, it has been considered to produce margarine having the same texture as butter by applying the same production method as butter to margarine. However, although the chewing method produces margarine with a better texture than the rapid cooling and softening method, the process is quite complicated. In addition, during the extraction of fat granules, excess water and some of the water-soluble components are also lost, resulting in a large loss of raw materials. Furthermore, the risk of bacterial contamination during production is greater than with the quenching method and sanitary control is difficult. For this reason, at present, this method is not used except for some high-grade margarines. The present inventors have so far conducted various studies with the aim of developing a manufacturing method that is a simple process similar to the usual rapid cooling and quenching method and that can produce margarine with good texture. As a result, by using a specific emulsifier and protein and keeping the ratio of oil phase to water phase at a specific ratio, stable O/
It becomes a W/O emulsification state, and then is cooled and worked in a rapid cooling/warming device, whereby the excess water is reversed to a W/O emulsion without separation, and a homogeneous margarine-like emulsion composition is obtained. Moreover, they discovered that this composition has an excellent texture and completed the present invention. That is, the present invention provides an aqueous phase containing 0.2 to 2.0% by weight of sucrose fatty acid ester with HLB of 11 or more based on the total amount of the composition, and 0.2 to 3.0% by weight of milk protein and/or vegetable protein based on the total amount of the composition. ,
The completely molten oil phase is pre-emulsified into an oil-in-water type with a volume ratio of 15/85 to 45/55, and the pre-emulsified liquid is rapidly cooled. The present invention relates to a method for producing a water-in-oil emulsion composition, which is characterized in that the emulsification state is reversed to W/O emulsion by mixing to obtain a product having homogeneous plasticity. The sucrose fatty acid ester used in the present invention must be mainly a monoester and have an HLB of 11 or more. As for the types of constituent fatty acids, those whose main components are stearic acid and palmitic acid are preferred. Milk protein and/or vegetable protein are used as the protein. Milk protein is generally added in the form of milk, concentrated milk, powdered milk, or fermented milk, but preparations such as casein or sodium caseinate can also be used. Soybean protein is a plant protein.
Peanut protein etc. can be used. Sucrose fatty acid esters and proteins with HLB of 11 or higher are essential components to maintain stable O/W emulsification during pre-emulsification and to enhance the texture of the product after rapid cooling and quenching. If the ratio of sucrose fatty acid ester is less than 0.2% by weight or the ratio of protein is less than 0.2% by weight, a stable O/W emulsion will not be obtained during pre-emulsification, and therefore a product with good texture will not be obtained. do not have. On the other hand, if these components are in excess, rapid cooling will occur.
During heating, the reversal to W/O emulsification is not performed well and the product becomes separated. In order to achieve good conversion to W/O emulsification, the upper limit of the sucrose fatty acid ester ratio is 2.0% by weight, and the upper limit of the protein ratio is 3.0% by weight. Furthermore, sucrose fatty acid ester
HLB is also important for maintaining O/W emulsification and enhancing texture. If the HLB of the sucrose fatty acid ester is lower than 11, O/W emulsification cannot be maintained during preliminary emulsification, resulting in poor texture of the product. In order to maintain O/W emulsification during pre-emulsification and to successfully convert to W/O emulsification during rapid cooling and quenching, the volume ratio of the oil phase to the water phase is also determined by weight. In the present invention, in order to maintain a good O/W emulsification state during preliminary emulsification, the volume ratio of the aqueous phase must be at least 15/15/
Must be greater than 85. If the volume ratio of the aqueous phase is lower than this, the emulsification state may reverse to a W/O emulsion or become unstable, or the pre-emulsion may significantly thicken. On the other hand, O/W
There is an upper limit to the ratio of the aqueous phase in order to completely invert the emulsion into a W/O emulsion during rapid cooling and quenching of the pre-emulsified liquid. If the temperature is too high, the product will not turn into a W/O emulsion during rapid cooling/warming. The oils and fats used in the present invention include natural animal and vegetable oils, their hydrogenated oils, fractionated oils, transesterified oils, etc., and these can be used in any combination. The hardness of fats and oils is the same as regular butter or margarine, with a melting point of 40℃ or less, and a hardness of 10 to 40℃ at room temperature.
% of solid fat and have plasticity are preferred. As the emulsifier, in addition to sucrose fatty acid ester, glycerin fatty acid ester, lecithin, sorbitan fatty acid ester, propylene glycol fatty acid ester, etc. can be used as necessary. As other ingredients, carbohydrates can be added in sweet spreads or butter cream products. Further, in order to improve the flavor, flavoring ingredients such as eggs, flavoring agents, and coloring agents can be freely used. In the method of the present invention, a pre-emulsified O/W emulsion is reversed to a W/O emulsion by rapid cooling and summing to obtain a product. Pre-emulsification is carried out by adding the oil phase little by little into the water phase while stirring to disperse and emulsify. After adding the oil phase, continue stirring to prevent separation of the oil phase and stabilize the emulsification. Although any type of stirrer can be used, a stirrer that rotates at high speed and has a strong shearing force achieves better emulsification. After emulsifying with a conventional stirrer, it is also possible to homogenize using a high-pressure homogenizer or the like to make the particle size uniform. During pre-emulsification, it is necessary to add the oil phase in a completely dissolved state to the aqueous phase, and to maintain the pre-emulsified liquid at a temperature at which the oil phase does not crystallize until it is rapidly cooled and homogenized. For rapid cooling and quenching after preliminary emulsification, it is preferable to use a continuous closed type quenching and quenching apparatus, as in the case of ordinary margarine. Continuous sealed quenching for margarine production
Japanese equipment is currently sold under various names both domestically and internationally, but all have the same basic structure, which is a combination of a cooling unit consisting of an internally scraped heat exchanger and a working unit using a pin machine. It is. In the present invention, any margarine manufacturing apparatus of this type can be used, and general margarine manufacturing equipment can be used as is. In rapidly cooling and summing the pre-emulsified liquid, it is first necessary to sufficiently cool the emulsified liquid using a cooling unit in order to reverse the emulsification state from O/W emulsification to W/O emulsification. If the cooling at this time is weak, the crystallization of the fat and oil will not be sufficient, and the reversal of the emulsification will be insufficient even in the subsequent sintering. In order to completely reverse the emulsification and obtain a uniform W/O emulsified product, it is desirable that the product temperature at the outlet of the cooling unit be lower than the temperature at which the SFI of the raw material fat is 15. The pre-emulsified liquid coming out of the cooling unit is still an O/W emulsion at this stage, and is then summed by the working unit and reversed to a W/O emulsion. At this time, the time during which the emulsification is applied has a great influence on the emulsified state. In other words, if the mixing time is too short, the emulsification will not be reversed sufficiently and the product will tend to separate. Conversely, if the mixing time is too long, the product will be subjected to even longer working hours even after the emulsification is reversed. If the product is kneaded too much, the fat globules will be completely destroyed, making it impossible to obtain a product with the excellent texture that is the object of the present invention.
The integration time in the working unit is determined by its capacity and product flow rate. In order to obtain a product that is uniform without separation and has a good texture, the product flow rate should be adjusted so that the working unit volume/product flow rate (i.e. average residence time) is in the range of 60 seconds to 180 seconds. It is desirable to set this. The products manufactured according to the present invention can be manufactured by ordinary quenching.
Compared to margarine produced by the Japanese method, it has a better taste and does not have the waxy texture characteristic of plastic fats and oils. Furthermore, even when compared with margarine or butter produced by the churning method, the product produced by the method of the present invention has a texture that is actually superior to both. Furthermore, when comparing the manufacturing processes, the present invention does not require complicated operations such as the turning method, and the steps corresponding to the crystallization of the O/W emulsion, the turning, and the sintering in the turning method are successively performed. Since the process is carried out in a closed system, there is no need to remove excess water from the system. Moreover, in terms of equipment, it is possible to use existing margarine production equipment with almost no modification, which is industrially advantageous. The product according to the invention has an excellent texture and is suitable for use as a spread on bread or as a sandwich. Further, the product according to the present invention can be whipped with a mixer or the like and used as butter cream in the same way as ordinary margarine. In the present invention, a good product can be obtained if the oil phase part is 60% or more by volume, so it is possible to make a product with a lower oil content than ordinary margarine or butter, and from a health standpoint, it is possible to produce a good product. It is more advantageous than butter and margarine. Examples of the present invention will be shown below, and the effects of the present invention will be explained in detail using comparative experimental examples. Example 1 A water-in-oil emulsion composition was manufactured using the following formulation. (Oil phase) Hydrogenated rapeseed oil (melting point 37℃) 50Kg Palm oil 35Kg Soybean oil 15Kg Monoglyceride (mainly stearic acid) 50g Soy lecithin 100g Butter flavor 30g (Aqueous phase) Water 55Kg Skim milk powder 5Kg Sucrose fatty acid ester (HLB16, Stearic acid (main component) 1Kg Salt 2Kg With this formulation, the volume ratio of the water phase/oil phase was 35/65. In addition, the SFI of the oil phase containing the emulsifier is at 15℃.
It was 21.7. The manufacturing method involved first raising the temperature of each oil and fat to 70°C or higher to melt them, mixing them, then adding monoglyceride and soybean lecithin and completely dissolving them at 70°C or higher.
The oil phase was then cooled to 60-65°C and butter flavor was added and subsequently maintained at this temperature. Meanwhile, an aqueous phase was prepared by adding skim milk powder, sucrose fatty acid ester, and salt to water and raising the temperature to 70°C to completely dissolve them. Next, the oil phase is gradually added while stirring the water phase with a stirrer with turbine-like stirring blades rotating at 800 rpm.
Thereafter, preliminary emulsification was performed by continuing stirring while maintaining the temperature at 60 to 65°C for an additional 30 minutes or more. The preliminary emulsion thus obtained was an O/W emulsion. Next, this preliminary emulsion was rapidly cooled and combined using the combinator described below to obtain the desired W/O emulsion product. This combinator is a continuous closed type rapid cooling and softening machine consisting of two cooling units and one working unit. The operating conditions for this combinator were a product flow rate of 70 kg/hr, and the refrigerant temperature was adjusted so that the product temperature at the outlet of A unit was 5°C. The calculated average residence time in the working unit at this time was 110 seconds. The product obtained by the above procedure has an appearance similar to margarine or butter, and has a temperature of 15 to 25℃.
It had good spreadability. Moreover, the texture was not waxy like that of general margarine, and had a good salty and milky taste, and an extremely preferable texture. Example 2 A water-in-oil emulsion composition was manufactured using the following formulation. (Oil phase) Hydrogenated fish oil (melting point 32℃) 75Kg Soybean oil 25Kg Monoglyceride (mainly stearic acid, oleic acid, IV50) 100g Soy lecithin 100g Butter flavor 30g (Aqueous phase) Water 60Kg Soy protein 1Kg Sucrose fatty acid Ester (HLB14, mainly stearic acid) 1Kg Sugar 30Kg Milk flavor 200g The volume ratio of the aqueous phase/oil phase in this formulation was 42/58. The SFI of the oil phase was 23.5 at 10°C. The product produced using the above formulation in exactly the same manner as in Example 1 had the same good product condition and texture as the product in Example 1, and was extremely desirable as a sweet spread. . Furthermore, the buttercream obtained by whipping this product was in good condition and had a very good texture compared to ordinary buttercream. Example 3 A water-in-oil emulsion composition was manufactured using the following formulation. (Oil phase) Hydrogenated rapeseed oil (melting point 37℃) 40Kg Butter oil 40Kg Corn oil 20Kg Monoglyceride (same as Example 1) 100g Soybean lecithin 100g Butter flavor 20g (Aqueous phase) Water 70Kg Skimmed milk powder 3Kg Sodium caseinate 1Kg Sugar Fatty acid ester (HLB16, mainly stearic acid) 0.8Kg Salt 2Kg With this composition, the volume ratio of water phase/oil phase was 40/60. In addition, the SFI of the oil phase containing the emulsifier is at 15℃.
It was 24.5. In the manufacturing method, an oil phase and an aqueous phase were first prepared and pre-emulsified in the same manner as in Example 1. Next, this pre-emulsified liquid is pressurized with an M-type homogenizing valve using a high-pressure homogenizing machine.
It was homogenized at 50Kg/cm 2 . Next, this homogenized liquid was passed through a combinator in the same manner as in Example 1 to obtain a water-in-oil emulsion composition. The resulting product had a flavor very similar to butter and had a better texture than butter. It also spreads better than butter,
It was extremely desirable as a product for spreading. Comparative Experimental Example 1 A series of experiments were conducted by preparing emulsions of experiment numbers 1 to 5 by changing the amount of sucrose fatty acid ester added. The formulation of all components other than sucrose fatty acid ester is the same as in Example 1. Furthermore, the same type of sucrose fatty acid ester as in Example 1 was used.
The manufacturing method was also the same as in Example 1. Table 1 shows the amount of sucrose fatty acid ester added and the experimental results in each experiment. Among these, experiment number 3 corresponds to that described in Example 1. In Experiment No. 1, the ratio of sucrose fatty acid ester was below the lower limit of the amount required by the present invention. In this case, as shown in Table 1, O/W emulsification cannot be maintained during preliminary emulsification, resulting in poor texture. Conversely, in Experiment No. 5 in which the ratio of sucrose fatty acid ester exceeds the upper limit of the present invention, a W/O emulsified product cannot be obtained by rapid cooling and summing. On the other hand, in Experiment Nos. 2, 3, and 4, the ratio of sucrose fatty acid ester was within the range of the present invention. In Experiment No. 2, where the ratio was close to the lower limit, the pre-emulsified state was somewhat unstable, but the effect of the present invention was recognized on the texture. Further, in Experiment No. 4, where this ratio is close to the upper limit, the product condition is somewhat poor, but it is within a practical range. Hereinafter, W/O indicates water-in-oil emulsification, and O/W indicates oil-in-water emulsification.

【表】 比較実験例 2 予備乳化液の乳化状態をO/Wにした場合と
W/Oにした場合の比較テストを行なつた。 実験番号3は実施例1と同じものである。 実験番号6は実験番号3の配合で、予備乳化方
法のみを変え、油相中に撹拌しながら水相を添加
することにより予備乳化を行なつたものである。
実験番号3と6の結果を表−2に示す。 実験番号6では予備乳化状態は不安定なW/O
になる。これを急冷〓和すると実験番号3と同じ
冷却条件であるのに冷却ユニツトの出口での品温
が高い。このことは冷却ユニツトの撹拌によつて
すでに製品が〓和され、潜熱放出が起きているこ
とを示す。得られた製品の食感は実験番号3と異
なりワキシーで呈味が弱く、通常のマーガリンと
大差がなかつた。
[Table] Comparative Experimental Example 2 A comparative test was conducted when the emulsification state of the pre-emulsified liquid was changed to O/W and W/O. Experiment number 3 is the same as Example 1. Experiment No. 6 was the formulation of Experiment No. 3, except that only the preliminary emulsification method was changed, and preliminary emulsification was carried out by adding the aqueous phase to the oil phase while stirring.
The results of experiment numbers 3 and 6 are shown in Table-2. In experiment number 6, the pre-emulsified state was unstable W/O
become. When this is combined with rapid cooling, the product temperature at the outlet of the cooling unit is high even though the cooling conditions are the same as in Experiment No. 3. This indicates that the product has already been homogenized by the agitation of the cooling unit and latent heat release has occurred. Unlike Experiment No. 3, the texture of the obtained product was waxy and had a weak taste, and was not much different from normal margarine.

【表】 *1 乳化状態が粗く、攪拌を止めるとすみ
やかに分離する。
比較実験例 3 実験番号3をもとにして、乳蛋白質の量を変え
て実験番号7〜10までの一連の実験を行なつた。
配合は脱脂粉乳、カゼインナトリウムの添加量を
除きすべて実験番号3と同じである。また製法も
実験番号3と同様に行なつた。各実験の乳蛋白質
の比率および実験結果を表−3に示す。 実験番号7は乳蛋白質の比率が本発明の下限値
より少ない。この場合は予備乳化時安定なO/W
が維持できず、食感が不良である。また乳蛋白質
の比率が上限値以上である実験番号10では製品の
離水が多く実用に耐えない。これに対して実験番
号8、3、9では乳蛋白質の比率が本発明の範囲
内にあり、いずれも満足し得る結果を得た。
[Table] *1 The emulsification is rough and separates quickly when stirring is stopped.
Comparative Experimental Example 3 Based on Experiment No. 3, a series of experiments No. 7 to No. 10 were conducted by changing the amount of milk protein.
The formulation was all the same as Experiment No. 3 except for the amounts of skim milk powder and sodium caseinate added. The manufacturing method was also the same as in Experiment No. 3. Table 3 shows the milk protein ratio and experimental results for each experiment. In Experiment No. 7, the ratio of milk protein was lower than the lower limit of the present invention. In this case, stable O/W during pre-emulsification
cannot be maintained and the texture is poor. In addition, in experiment number 10 where the ratio of milk protein was above the upper limit, the product had too much syneresis and was not suitable for practical use. On the other hand, in Experiment Nos. 8, 3, and 9, the ratio of milk protein was within the range of the present invention, and satisfactory results were obtained in all cases.

【表】 *2 わずかに水滴の分離がある。
*3 多量の水滴が分離している。
比較実験例 4 実験番号3をもとにして、水の添加量を変えて
実験番号11〜14までの一連の実験を行なつた。水
以外の成分の配合および製造方法は実験番号3と
同じである。各実験における水相/油相の容量比
および実験の結果を表−4に示す。 実験番号11は水相の容量比が本発明の下限値よ
り低くなつている。この場合は予備乳化時の乳化
状態はO/Wであるが予備乳化液の粘度が非常に
高く乳化状態が不良で急冷〓和が行ないにくい。
また得られた製品の食感も不満足なものである。 実験番号13では逆に水相の比率が本発明の上限
値より高い。この場合は予備乳化液は良好なO/
Wであるが、急冷〓和によつてもW/Oの製品が
得られない。 これに対して、実験番号3および12、13は水相
の容量比が本発明の範囲内にあり、満足し得る実
験報告を得ている。
[Table] *2 There is slight separation of water droplets.
*3 A large amount of water droplets are separated.
Comparative Experimental Example 4 Based on Experiment No. 3, a series of experiments No. 11 to No. 14 were conducted by changing the amount of water added. The blending of components other than water and the manufacturing method were the same as in Experiment No. 3. Table 4 shows the volume ratio of water phase/oil phase in each experiment and the results of the experiment. In Experiment No. 11, the volume ratio of the aqueous phase was lower than the lower limit of the present invention. In this case, the emulsification state during pre-emulsification is O/W, but the viscosity of the pre-emulsified liquid is very high and the emulsification state is poor, making it difficult to perform rapid cooling/warming.
Moreover, the texture of the obtained product is also unsatisfactory. In Experiment No. 13, on the contrary, the ratio of the aqueous phase was higher than the upper limit of the present invention. In this case, the pre-emulsified liquid has good O/
Although it is W/O, a W/O product cannot be obtained even by rapid cooling and merging. On the other hand, in Experiment Nos. 3, 12, and 13, the volume ratio of the aqueous phase was within the range of the present invention, and satisfactory experimental reports were obtained.

【表】【table】

Claims (1)

【特許請求の範囲】[Claims] 1 HLB11以上のシヨ糖脂肪酸エステルを組成
物全量に対して0.2〜2.0重量%、乳蛋白質およ
び/または植物蛋白質を組成物全量に対して0.2
〜3.0重量%含有する水相部と、完全に溶融した
状態にある油相部を、両者の容量比が水相部/油
相部=15/85〜45/55になる組成で水中油型に予
備乳化し、その予備乳化液を急冷〓和することに
より乳化状態を油中水型乳化に反転させて、均質
な可塑性を有する製品を得ることを特徴とする、
油中水型乳化組成物の製造法。
1 0.2 to 2.0% by weight of sucrose fatty acid ester with HLB11 or higher based on the total amount of the composition, and 0.2% of milk protein and/or vegetable protein based on the total amount of the composition.
An oil-in-water type with a composition in which a water phase containing ~3.0% by weight and an oil phase in a completely molten state have a volume ratio of water phase/oil phase = 15/85 to 45/55. The method is characterized by pre-emulsifying the pre-emulsified liquid and rapidly cooling and mulching the pre-emulsified liquid to reverse the emulsified state to a water-in-oil emulsion to obtain a product having homogeneous plasticity.
A method for producing a water-in-oil emulsion composition.
JP58105677A 1983-06-15 1983-06-15 Preparation of water-in-oil type emulsified composition Granted JPS59232048A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58105677A JPS59232048A (en) 1983-06-15 1983-06-15 Preparation of water-in-oil type emulsified composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58105677A JPS59232048A (en) 1983-06-15 1983-06-15 Preparation of water-in-oil type emulsified composition

Publications (2)

Publication Number Publication Date
JPS59232048A JPS59232048A (en) 1984-12-26
JPH0342866B2 true JPH0342866B2 (en) 1991-06-28

Family

ID=14414058

Family Applications (1)

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

Country Link
JP (1) JPS59232048A (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH069462B2 (en) * 1985-05-27 1994-02-09 日本油脂株式会社 Liquid margarine
JPS62215342A (en) * 1986-03-14 1987-09-22 Nippon Oil & Fats Co Ltd Baking fat or oil composition
GB8620897D0 (en) * 1986-08-29 1986-10-08 Unilever Plc Emulsions with reduced fat content
GB8713266D0 (en) * 1987-06-05 1987-07-08 Unilever Plc Edible dispersion
JP5075085B2 (en) * 2008-10-21 2012-11-14 キユーピー株式会社 Water-in-oil aerated food
JP2010104946A (en) * 2008-10-31 2010-05-13 Riso Kagaku Corp Water-in-oil (w/o) emulsion formed using reverse vesicle

Also Published As

Publication number Publication date
JPS59232048A (en) 1984-12-26

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