JPH01242133A - Powdered emulsifier composition and its production - Google Patents

Powdered emulsifier composition and its production

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Publication number
JPH01242133A
JPH01242133A JP63064739A JP6473988A JPH01242133A JP H01242133 A JPH01242133 A JP H01242133A JP 63064739 A JP63064739 A JP 63064739A JP 6473988 A JP6473988 A JP 6473988A JP H01242133 A JPH01242133 A JP H01242133A
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JP
Japan
Prior art keywords
powdered
parts
emulsifier
added
water
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.)
Pending
Application number
JP63064739A
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Japanese (ja)
Inventor
Keiichi Kani
可児 佳一
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Individual
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Individual
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Priority to JP63064739A priority Critical patent/JPH01242133A/en
Publication of JPH01242133A publication Critical patent/JPH01242133A/en
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  • Confectionery (AREA)
  • Bakery Products And Manufacturing Methods Therefor (AREA)
  • General Preparation And Processing Of Foods (AREA)
  • Noodles (AREA)
  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)

Abstract

PURPOSE:To eliminate solidification of powder due to moisture absorption by mixing polyglycerine fatty acid ester, etc., and anhydrous crystalline maltose each in specified amt. without water and by powdering them to prepare an emulsifier compsn. CONSTITUTION:The powdered emulsifier compsn. is prepd. by adding 50-500 pts.wt. anhydrous crystalline maltose to 100 pts.wt. polyglycerine fatty acid ester and(or) polyoxyethylene(20)sorbitan fatty acid ester, by mixing them without water, by solidifying and thereafter by powdering. The compsn. can be compounded with alcohol, animal and vegetable oil having <=30 deg.C melting point, etc. The obtd. powdered emultsifier compsn. can be used for the addition to food and food material such as for increasing cold-water dispersibility of powdered cocoa, preventing the decrease of consistency of chocolate.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、食品ないし食品原料に配合し易い粉末状乳化
剤組成物及びその製造法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a powdery emulsifier composition that can be easily incorporated into foods or food raw materials, and a method for producing the same.

〔従来の技術及び問題点〕[Conventional technology and problems]

ポリグリセリン脂肪酸エステル(以下、ポリグリセリン
エステルと略称する)、ポリオキシエチレン(20)ソ
ルビタン脂肪エステル(以下、ポリソルベートと略称す
る)は、食品に、乳化、分散、浸透、湿潤、起泡、消泡
、でんぷんの改質などの目的で使用される。しかし、食
品への添加量は殆どの場合0.1〜0.5重量%ときわ
めて少量であり、食品に均一に添加するには、多大な技
術を要する。それは、ポリグリセリンエステル、ポリソ
ルベートは、常温で粘稠な液体ないしにかわ状固体であ
るためで特に粉末状食品ないし食品製造工程において粉
末状で添加することが求められる食品においては、これ
らを少量均一に分散混合することがきわめて困難であっ
た。
Polyglycerin fatty acid ester (hereinafter abbreviated as polyglycerin ester) and polyoxyethylene (20) sorbitan fatty ester (hereinafter abbreviated as polysorbate) are used to emulsify, disperse, penetrate, moisturize, foam, and defoam in foods. , used for purposes such as modifying starch. However, the amount added to food is extremely small, 0.1 to 0.5% by weight in most cases, and a great deal of skill is required to uniformly add it to food. This is because polyglycerin esters and polysorbates are viscous liquids or glue-like solids at room temperature, so they must be added uniformly in small amounts to foods that are powdered or require them to be added in powdered form during the food manufacturing process. Dispersion mixing was extremely difficult.

このため、従来は、これら乳化剤を60〜80℃に加熱
溶解し、粘度を低くした液体として加えるか、この液体
品をデキストリン等と混合して粉末化したり、カゼイン
ナトリウム、デキストリン等を用いて乳化後噴霧乾燥し
て粉末した後加える方法が一般的であった。
For this reason, in the past, these emulsifiers were dissolved by heating at 60 to 80°C and added as a liquid with a lower viscosity, or this liquid product was mixed with dextrin and the like to form a powder, or emulsified using sodium caseinate, dextrin, etc. The common method was to spray dry the powder and then add it to the powder.

しかし、加温して粘度を下げた液状として食品に加えて
も例えば水産練り製品のように製造温度が10℃以下の
低温の場合は、加えた途端固化してしまい、均一には分
散し難たい。
However, even if you add it to food as a liquid that has been heated to lower its viscosity, if the manufacturing temperature is low (10°C or less, such as in seafood paste products), it will solidify as soon as it is added, making it difficult to disperse it uniformly. sea bream.

又、デキストリンで粉末化する方法では、これら乳化剤
に均一な被膜を作るのが難しく、さらに粉末化基剤が水
に不溶性の場合は、乳化剤の効果が充分に発揮しえない
Furthermore, in the method of powdering with dextrin, it is difficult to form a uniform coating on these emulsifiers, and if the powder base is insoluble in water, the effect of the emulsifier cannot be fully exhibited.

カゼインナトウリム、デキストリン等を用いて噴切乾燥
し粉末化する方法は、これらの中で最も好ましい方法で
あるが、乳化用の配合割合に制限があり高温度の粉末に
することが難しい。さらにこの噴霧乾燥品は、水に加え
た場合に乳化白濁して透明に溶けない。又、PHが低い
食品例えば、粉末ジュース、粉末ドレッシング等ではカ
ゼインが等電点で沈澱してしまうので添加できない。
The method of blow-drying and powdering using caseinate sodium, dextrin, etc. is the most preferable method among these methods, but there are restrictions on the blending ratio for emulsification and it is difficult to make powder at high temperature. Furthermore, when this spray-dried product is added to water, the emulsion becomes cloudy and does not dissolve transparently. Furthermore, casein cannot be added to foods with low pH, such as powdered juices and powdered dressings, because casein will precipitate at the isoelectric point.

従って、ポリグリセリンエステル、ポリソルベートを粉
末化するには広いPH領域の水に透明に溶解し、粉末等
では吸温性の少ない粉末化基剤が求められていた。
Therefore, in order to powderize polyglycerol esters and polysorbates, there has been a need for a powdering base that is transparently soluble in water over a wide pH range and has low heat absorbing properties when used as a powder.

〔問題を解決するための手段〕[Means to solve the problem]

そこで、本発明者は、ポリグリセリンエステル、ポリソ
ルベートを粉末化する基剤を鋭意研究した結果、食品と
しても好ましい無水結晶マルトースが最適なことを見い
だし本発明を完成した。
Therefore, as a result of intensive research into the base material for powdering polyglycerin esters and polysorbates, the present inventors found that anhydrous crystalline maltose, which is also preferred as a food product, was optimal and completed the present invention.

無水結晶マルトースを用いて粉末化したポリグリセリン
エステル、ポリソルベートは、幅広いPHの水溶液に透
明に溶け、粉末時では吸温による固結が殆んど見られな
かった。
Polyglycerin ester and polysorbate powdered using anhydrous crystalline maltose were transparently dissolved in aqueous solutions with a wide pH range, and almost no caking due to heat absorption was observed when powdered.

本発明におけるポリグリセリンエステルの構造式は図1
に示すが、炭素数が6〜22の飽和及び不飽和脂肪酸と
グリセリンが3〜10ケ縮合したポリグリセリンとのエ
ステルである。脂肪酸は水酸基を持ったリシノール酸の
縮合したものでも良い。これらの常温における外観は、
脂肪酸がカプロン酸、カプリル酸、カプリン酸、ラウリ
ン酸、オレイン酸、リノール酸、縮合リシノレイン酸、
の場合は、粘稠な液体であり、脂肪酸がミリスチン酸、
バルミチン酸、ステプリン酸、プラキドン酸、ベヘン酸
の場合は、融点40〜70℃のにかわないしフックス状
固体である。エステル化度はモノエステル〜デカエステ
ルまで含まれるが、モノエステル含量の多いものが好ま
しい。
The structural formula of the polyglycerin ester in the present invention is shown in Figure 1.
This is an ester of polyglycerin, which is a condensation of saturated or unsaturated fatty acids having 6 to 22 carbon atoms and 3 to 10 glycerins. The fatty acid may be a condensed product of ricinoleic acid having a hydroxyl group. Their appearance at room temperature is
Fatty acids include caproic acid, caprylic acid, capric acid, lauric acid, oleic acid, linoleic acid, condensed ricinoleic acid,
In the case of , it is a viscous liquid and the fatty acids are myristic acid,
In the case of valmitic acid, stepric acid, plachydonic acid, and behenic acid, they are sticky or fuchsia solids with a melting point of 40 to 70°C. The degree of esterification ranges from monoester to decaester, but those with a high monoester content are preferred.

本発明におけるポリソルベートの構造式は、図2に示す
が、ソルビトールを加熱して1分子中より1分子の水を
脱水したソルビタン、2分子を脱水したソルバイド、未
脱水のソルビトールの脂肪酸エステルの酸化エチレン付
加物である。脂肪酸は炭素数6〜22の飽和及び不飽和
脂肪酸で、酸化エチレンの付加モル数は、ソルビトール
、ソルビタン、ソルバイドの脂肪酸エステル1モルに付
き、平均20モルである。エステル化度はモノ、ジ、ト
リ、テトラの混合物であるがモノエステル含量が多い方
が好ましい。これらポリソルベートの常温における外観
は、脂肪酸がカプロン酸、カプリル酸、カプリン酸、ラ
ウリン酸、オレイン酸の場合は、粘稠な液体、脂肪酸が
ミリスチン酸、バルミチン酸、ステプリン酸、アラキド
ン酸、ベヘン酸の場合は、粘稠な液体ないしゲル状固体
である。
The structural formula of polysorbate in the present invention is shown in Figure 2. Sorbitan is obtained by heating sorbitol to dehydrate one molecule of water, sorbide is obtained by dehydrating two molecules, and ethylene oxide of fatty acid ester of undehydrated sorbitol. It is an appendage. The fatty acids are saturated and unsaturated fatty acids having 6 to 22 carbon atoms, and the number of moles of ethylene oxide added is on average 20 moles per mole of fatty acid ester of sorbitol, sorbitan, and sorbide. The degree of esterification is a mixture of mono-, di-, tri-, and tetra-esterification, but a higher monoester content is preferred. The appearance of these polysorbates at room temperature is viscous liquid when the fatty acids are caproic acid, caprylic acid, capric acid, lauric acid, and oleic acid; If so, it is a viscous liquid or gel-like solid.

本発明における粉末化基剤である無水結晶マルトースは
、グルコースが2分子α−1、4結合したもので通常の
結昇マルトースは、1分子の結晶水を持つのに対し、結
晶水を持たない。従って無水結晶マルトースは、1モル
当たり1モル(重量%で約5%)の水を吸収して固化す
るので、水分を含む食品例えばバター(水分16%)、
醸造酢(水分60%)、等の粉末化基剤としてすでに知
られている。しかし、水分を含まない食品例えばラー油
を粉末化するには水分を加えないと出来ない。しかしな
がら、本発明者は、ポリグリセリンエステル及び/又は
ポリソルベートに無水結晶マルトースを加えて粉末化す
る際に、水分をくわえなくても固化し、これを粉砕する
ことによって良好な粉末が得られることを見いだした。
Anhydrous crystalline maltose, which is the powder base in the present invention, is composed of two molecules of glucose bonded with α-1,4 bonds, and ordinary crystalline maltose has one molecule of crystal water, but does not have crystal water. . Therefore, anhydrous crystalline maltose absorbs 1 mole of water per mole (approximately 5% by weight) and solidifies, so it can be used in foods containing moisture, such as butter (16% moisture).
It is already known as a powder base for brewed vinegar (60% moisture), etc. However, food that does not contain water, such as chili oil, cannot be turned into powder without adding water. However, the present inventor has found that when adding anhydrous crystalline maltose to polyglycerin ester and/or polysorbate and powdering it, it solidifies without adding water, and that a good powder can be obtained by pulverizing it. I found it.

この理由としては、ポリグリセリン中の水酸基(−OH
)、エーテル状美素(−o−)、ポリソルベート中の酸
化エチレン酸に由来するエーテル状酸素(−o−)は、
いずれも水との強て親和力があるので、無水結晶マルト
ースに対しあたかも水分子の水酸基(−OH)と同じよ
うに反応して結合するものと考えられる。
The reason for this is that the hydroxyl group (-OH
), ethereal oxygen (-o-), ethereal oxygen (-o-) derived from ethylene oxide in polysorbate,
Since both have a strong affinity for water, they are thought to react and bond to anhydrous crystalline maltose in the same way as the hydroxyl group (-OH) of a water molecule.

本発明においてポリグリセリンエステル及び/又はポリ
ソルベート100重量部に対し無水結晶マルトースを5
0〜500重量部使用するのが好ましい。無水結晶マル
トースが50重量部より少ないと、粉末のサラサラした
状態を保ちにくく、500重量部より多いと、ポリグリ
セリンエステル、ポリソルベートの割合が少なくなるの
で好ましくない。更に必要であれば、エクルール、プロ
ピレングリコール、グリセリンのようなアルコール、融
点30℃以下の動植物油脂例えば魚油、ヤシ油、バター
オイル、フレーバーオイル、大豆油、ナタネ油、サフラ
ワー油、ゴマ油、月見草油、中鎮脂肪酸トリグリセライ
ドなど、更にレシチン、グリセリン脂肪酸エステル、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、ショ糖脂肪酸エステル、有機酸モノグリセラ
イドなどの乳化剤を加えることも出来る。
In the present invention, 5 parts by weight of anhydrous crystalline maltose is added to 100 parts by weight of polyglycerol ester and/or polysorbate.
Preferably, 0 to 500 parts by weight are used. If the amount of anhydrous crystalline maltose is less than 50 parts by weight, it will be difficult to maintain the smooth state of the powder, and if it is more than 500 parts by weight, the proportion of polyglycerin ester and polysorbate will decrease, which is not preferable. In addition, if necessary, alcohols such as eclur, propylene glycol, and glycerin, animal and vegetable oils and fats with a melting point below 30°C, such as fish oil, coconut oil, butter oil, flavor oil, soybean oil, rapeseed oil, safflower oil, sesame oil, and evening primrose oil. , neutral fatty acid triglyceride, etc. Furthermore, emulsifiers such as lecithin, glycerin fatty acid ester, sorbitan fatty acid ester, propylene glycol fatty acid ester, sucrose fatty acid ester, organic acid monoglyceride, etc. can also be added.

本発明組成物の用途としては、ポリグリセリンエステル
及び/又はポリソルベートの効果を期待して用いる食品
及び食品原料であり、例えば粉末ココアの冷水分散性の
向上、チョコレートの粘度低下、粉末ジュースの香料の
可溶化、粉末ドレッシングの乳化性の向上、パン、パン
ミックス、ケーキ、ケーキミックス、ドーナッツ、ドー
ナッツミックス、麺等のでんぷんを主成分とする食品の
品質改良、アイスクリーム用乳化安定剤、粉末コーヒー
クリームの乳化、分散性の向上、粉末ホイップクリーム
の起泡性の向上、水産練り製品の白度向上、冷凍スリ身
の変性防止、ソーセージのケーシングの剥離性の向上、
豆腐の製造時の消泡等が挙げられるが、本発明組成物は
、ここに記載した食品にその用途が限定されるものでは
ない。
Applications of the composition of the present invention include foods and food raw materials that are expected to have the effects of polyglycerin esters and/or polysorbates, such as improving the cold water dispersibility of powdered cocoa, reducing the viscosity of chocolate, and adding flavor to powdered juices. Solubilization, improvement of emulsifying properties of powdered dressings, quality improvement of starch-based foods such as bread, bread mixes, cakes, cake mixes, donuts, donut mixes, noodles, emulsion stabilizers for ice cream, powdered coffee cream Improving the emulsification and dispersibility of powdered whipped cream, improving the whiteness of seafood paste products, preventing denaturation of frozen surimi, improving the peelability of sausage casings,
Examples include defoaming during the production of tofu, but the use of the composition of the present invention is not limited to the foods described herein.

以下に本発明の実施例及び比較例をしめす。Examples and comparative examples of the present invention are shown below.

〔実施例〕〔Example〕

実施例1〜4 ポリグリセリンエステル、ポリソルベート、無水結晶マ
ルトースを表1の割合で、水を加えず配合し、固化後粉
砕して粉末を得た。
Examples 1 to 4 Polyglycerol ester, polysorbate, and anhydrous crystalline maltose were blended in the proportions shown in Table 1 without adding water, solidified, and then ground to obtain powder.

表1における成分名 A:デカグリセロールモノオレート B:ヘキサグリセロールモノステアレートC:ポリオキ
シエチレン(20)ソルビタンモノラウレート D:ポリオキシエチレン(20)ソルビタンモノステア
レート E:無水結晶マルトース 実施例1〜4の粉末をポリエチレン製の袋に入れ室温に
保存し、粉末の固結程度を調べた。さらに、この粉末を
1gをPH4の水溶液100mlに加えて、溶解性を調
べた。その結果表2の結果を得た。表2の結果からも明
らかなように、本発明による実施例1〜4は、粉末の外
観も良好で、保存による固結もなくPH4の水溶液に透
明に溶解した。
Component names in Table 1 A: Decaglycerol monooleate B: Hexaglycerol monostearate C: Polyoxyethylene (20) Sorbitan monolaurate D: Polyoxyethylene (20) Sorbitan monostearate E: Anhydrous crystalline maltose Example 1 The powders from No. 4 to 4 were placed in a polyethylene bag and stored at room temperature, and the degree of caking of the powders was examined. Further, 1 g of this powder was added to 100 ml of an aqueous solution of PH4 to examine solubility. As a result, the results shown in Table 2 were obtained. As is clear from the results in Table 2, the powders of Examples 1 to 4 according to the present invention had good appearance and were dissolved transparently in the PH4 aqueous solution without caking during storage.

〔比較例1〜4〕 比較例1として、表1の配合成分Aを100部デキスト
リン300部と混合して粉末とした。
[Comparative Examples 1 to 4] As Comparative Example 1, 100 parts of compounding component A in Table 1 were mixed with 300 parts of dextrin to form a powder.

比較例2として、表1の配合成分Bを50部、配合成分
Cを50部、でんぷん100部と混合した。
As Comparative Example 2, 50 parts of component B in Table 1, 50 parts of component C, and 100 parts of starch were mixed.

比較例3として、表1の配合成分Dを100部カゼイン
ナトリウム10部、デキストリン40部を図形分40%
になるよう60での温水に溶解し特殊機化工業製TKホ
モミキサーにて100V.3分乳化後、噴霧乾燥した。
As Comparative Example 3, 100 parts of compounding component D in Table 1, 10 parts of sodium caseinate, and 40 parts of dextrin were added to the graphic content of 40 parts.
Dissolve in warm water at 60V and mix at 100V using a TK homo mixer made by Tokushu Kika Kogyo. After emulsifying for 3 minutes, it was spray dried.

比較例4として、表1の配合成分Aを30分、配合成分
Dを70部、ガゼインナトリウム100部、デキストリ
ン400部を比較例3と同様の方法にて粉末とした。こ
れらの結果を表3に示す。
As Comparative Example 4, Component A in Table 1 was powdered for 30 minutes, 70 parts of Compound D, 100 parts of sodium caseinate, and 400 parts of dextrin were prepared in the same manner as in Comparative Example 3. These results are shown in Table 3.

表3の結果から、比較例では、粉末が良く出来ないか、
保存中に固結したり、PH4の水溶液に添加すると沈澱
が発生して実用性に劣った。
From the results in Table 3, it can be seen that the powder was not produced well in the comparative example.
It solidified during storage or precipitated when added to an aqueous PH4 solution, making it impractical.

〔実施例5〜8〕 必須成分として、ポリグリンエステル、ポリソルベート
、無水結晶マルトース、任意成分としてエタノール、大
豆油、レシチン、オレンジオイルを表4のような割合で
、水を加えずに混合して固化後粉砕して粉末を得た。
[Examples 5 to 8] Polyglycline ester, polysorbate, anhydrous crystalline maltose as essential components, and ethanol, soybean oil, lecithin, and orange oil as optional components were mixed in the proportions shown in Table 4 without adding water. After solidification, it was crushed to obtain a powder.

表4における成分名 F:ヘキサグリセロールベンタオレートG:テトラグリ
セロールモノステアレートH:ポリオキシエチレン(2
0)ソルビタンモノオレート I:ポリオキシエチレン(20)ソルビタンモノステア
レート J:無水結晶マルトース K:オレンジオイル 〔比較例5〜8〕 比較例5として、表4における配合成分F100部、デ
キストリン400部、エタノール50部レシチン50部
を混合して粉末化を試みたがペースト状となり粉末に成
らなかった。
Component names in Table 4 F: Hexaglycerol bentaorate G: Tetraglycerol monostearate H: Polyoxyethylene (2
0) Sorbitan monooleate I: Polyoxyethylene (20) Sorbitan monostearate J: Anhydrous crystalline maltose K: Orange oil [Comparative Examples 5 to 8] As Comparative Example 5, 100 parts of compounding component F in Table 4, 400 parts of dextrin, An attempt was made to make the mixture into a powder by mixing 50 parts of ethanol and 50 parts of lecithin, but the mixture became a paste and could not be made into a powder.

比較例6として、表4における配合成分G50部、配合
成分1を50部、大豆油を50部、カゼイン20部、デ
キストリン80部を比較例3の方法にて粉末化を試みた
が、良好な粉末が得らなかった。
As Comparative Example 6, an attempt was made to powderize 50 parts of Ingredient G in Table 4, 50 parts of Ingredient 1, 50 parts of soybean oil, 20 parts of casein, and 80 parts of dextrin by the method of Comparative Example 3, but no good results were obtained. No powder was obtained.

比較例7として、表4における配合成分H20部、配合
成分Iを80部、レシテンを25部、でんぷん300部
を混合して粉末を得た。
As Comparative Example 7, a powder was obtained by mixing 20 parts of component H in Table 4, 80 parts of component I, 25 parts of lecithene, and 300 parts of starch.

比較例8として、表4における配合成分H100部、エ
タノール30部、表4における配合成分K20部、カゼ
インナトリウム100部、デキストリン400部を比較
例3と同様の方法にて粉末とした。
As Comparative Example 8, 100 parts of component H in Table 4, 30 parts of ethanol, 20 parts of component K in Table 4, 100 parts of sodium caseinate, and 400 parts of dextrin were powdered in the same manner as in Comparative Example 3.

〔応用例1〜4〕 本発明による実施例5〜8、比較例7〜8を用いて、以
下の応用例1〜4を行った。
[Application Examples 1 to 4] The following Application Examples 1 to 4 were conducted using Examples 5 to 8 according to the present invention and Comparative Examples 7 to 8.

応用例1.粉末ココアの冷水分散性。Application example 1. Cold water dispersibility of powdered cocoa.

市販ココア(明治製菓(株)製)100gに本発明によ
る実施例5の粉末状乳化剤1gを粉末どうし良く混合し
た。コントロール1として、乳化剤無添加品、コントロ
ール2として、表4における配合成分F0.2g、エタ
ノール0.1g、レシチン0.1gを混合して、100
gの粉末ココアに加えた このようにして調製した粉末ココア10gを5〜10℃
の冷水100mlに加え、ココアが冷水中に分散、沈澱
する迄の時間を比較した。
1 g of the powdered emulsifier of Example 5 according to the present invention was thoroughly mixed with 100 g of commercially available cocoa (manufactured by Meiji Seika Co., Ltd.). Control 1 is a product with no emulsifier added, and Control 2 is a product containing 0.2 g of the ingredients F in Table 4, 0.1 g of ethanol, and 0.1 g of lecithin.
10 g of powdered cocoa thus prepared added to 10 g of powdered cocoa at 5-10°C.
was added to 100 ml of cold water, and the time taken for cocoa to disperse and precipitate in the cold water was compared.

表から明らかなように本発明による実施例5の粉末状乳
化剤組成物を粉末ココアに加えると、ココアの冷水への
分散、沈澱をはやめ乳化剤の効果が充分に発揮されてい
ることが分かる。乳化剤のみでは、粉末ココアに均一に
混合出来ず、したがって乳化剤の効果が発揮されていな
い。
As is clear from the table, when the powdered emulsifier composition of Example 5 according to the present invention is added to powdered cocoa, dispersion of cocoa in cold water and precipitation are stopped, and the effect of the emulsifier is fully exhibited. An emulsifier alone cannot be mixed uniformly into powdered cocoa, and therefore the effect of the emulsifier is not exhibited.

応用例2.パン 市販パンミックス(日清製粉(株)製)285gに本発
明による実施例6の粉末状乳化剤3gを粉末混合し、ナ
ショナル製自動パン焼き器によりマニュアルに従って、
山型パンを焼成した。コントロール1として、乳化剤無
添加、コントロール2として、表4における配合成分G
1g、表4における配合成分1を1g、大豆油1gを混
合しパンミックスに加え、以下同様にしてパンを焼成し
た。
Application example 2. 3 g of the powdered emulsifier of Example 6 according to the present invention was mixed with 285 g of a commercially available bread mix (manufactured by Nisshin Seifun Co., Ltd.), and the mixture was prepared using a National automatic bread maker according to the manual.
I baked mountain-shaped bread. Control 1: No emulsifier added; Control 2: Compounding component G in Table 4.
1 g of compounded component 1 in Table 4 and 1 g of soybean oil were mixed and added to the bread mix, and bread was baked in the same manner.

焼成後、室温まで冷却したパンの重さと体積(サランラ
ップで完全に密封包装し、水との置換法により測定)を
測定し比容積(cc/g)を求めた。次いで、室温に2
0時間放置後、厚さ2cmにスライスして、パンの内相
の柔らかさを比較した。
After baking, the bread was cooled to room temperature, and its weight and volume (completely sealed with Saran wrap and measured by the water displacement method) were measured to determine the specific volume (cc/g). Then at room temperature 2
After standing for 0 hours, the bread was sliced into 2 cm thick slices and the internal softness of the bread was compared.

表からも明らかなように、実施例6による乳化剤組成物
を添加したパンミックスを用いて焼成したパンは、乳化
剤無添加区のパンより約10%もパンの比容積が大きく
、またパンの内相も20時間後でも柔らかかった。一方
、乳化剤を大豆油と混合してパンミックスに加えた区は
、加えた乳化剤量は、実施例6より多いにもかかわらず
乳化剤の効果が充分に発揮されていない。これは、少量
の粘稠な液体が粉末のパンミックスに均一に混和してい
ないためと考えられる。
As is clear from the table, the bread baked using the bread mix to which the emulsifier composition of Example 6 was added had a specific volume that was about 10% larger than the bread without emulsifier. The phase was also soft even after 20 hours. On the other hand, in the case where the emulsifier was mixed with soybean oil and added to the bread mix, the effect of the emulsifier was not fully exhibited even though the amount of the emulsifier added was larger than that of Example 6. This is thought to be due to the small amount of viscous liquid not being uniformly mixed into the powdered bread mix.

応用例3.ホイップクリーム 市販粉末ホイップクリーム(雪印乳業(株)製)65g
に本発明による実施例7の粉末状乳化剤1.5gを混合
し、牛乳90mlを加え、ホイッパーで2分ホイップし
、オーバーランを測定する。
Application example 3. Whipped cream Commercially available powdered whipped cream (manufactured by Snow Brand Milk Products Co., Ltd.) 65g
1.5 g of the powdered emulsifier of Example 7 according to the present invention was mixed with the mixture, 90 ml of milk was added thereto, the mixture was whipped for 2 minutes with a whipper, and the overrun was measured.

コントロール1として、市販品そのまま、コントロール
2として、比較例7による粉末乳化剤1.5gを混合し
、同様の方法にてオーバーランを測定した。
As Control 1, the commercially available product was mixed as is, and as Control 2, 1.5 g of the powdered emulsifier according to Comparative Example 7 was mixed, and the overrun was measured in the same manner.

オーバーラン=A−B/B×100(%)A:100m
l容カップのホイップ前の重さB:100ml容カップ
のホイップ後の重さ表からも明らかなように、本発明に
より実施例7の粉末状乳化剤組成物を添加した区は、オ
ーバーランがコントロール1に比較して約2倍ときわめ
て良く起泡したが、比較例7の粉末状乳化剤組成物添加
区は、乳化剤の効果が全く発揮されていない。これは、
粉末化する基材であるでんぷんが水に溶けないためであ
る。
Overrun = A-B/B x 100 (%) A: 100m
Weight B of 1-volume cup before whipping: Weight after whipping of 100-ml cup As is clear from the table, overrun was controlled in the group to which the powdered emulsifier composition of Example 7 according to the present invention was added. Although foaming was extremely good, about twice as much as in Comparative Example 7, the effect of the emulsifier was not exhibited at all in the case of Comparative Example 7, in which the powdered emulsifier composition was added. this is,
This is because starch, which is the base material to be powdered, is not soluble in water.

応用例4.粉末ジュース 次の配合により粉末ジュースを製造した。Application example 4. powder juice A powdered juice was produced using the following formulation.

配合 ブドウ糖(無水) 100g クエン酸(無水) 1g 食用黄色4号 0.2g 実施例8、又は比較例8の粉末乳化剤 0.65g この粉末ジュース20gを5〜10℃の冷水100ml
に溶解した。
Blend Glucose (anhydrous) 100g Citric acid (anhydrous) 1g Food Yellow No. 4 0.2g Powdered emulsifier of Example 8 or Comparative Example 8 0.65g Add 20g of this powdered juice to 100ml of cold water at 5-10°C
dissolved in

表からあきらかなように、本発明による実施例8の粉末
状乳化剤組成物を配合した粉末ジュースは、オレンジオ
イルが乳化剤により可溶化して透明に溶けたが、比較例
8の乳化剤組成物を配合した粉末ジュースは、沈澱を生
じた。これは、クエン酸によるPHの低下により、比較
例8の粉末化基材であるカゼインナトリウムがカゼイン
になったためである。
As is clear from the table, in the powdered juice containing the powdered emulsifier composition of Example 8 according to the present invention, orange oil was solubilized by the emulsifier and dissolved transparently, but when the powdered juice was blended with the emulsifier composition of Comparative Example 8. The powdered juice produced precipitate. This is because sodium caseinate, which is the powdered base material of Comparative Example 8, turned into casein due to the decrease in pH due to citric acid.

〔発明の効果〕〔Effect of the invention〕

本発明による粉末状乳化剤組成物は、次のような効果が
見られる。
The powdered emulsifier composition according to the present invention has the following effects.

1.ポリグリセリンエステル、ポリソルベートの取扱い
がきわめて容易になり、特に粉末状食品ないし食品原料
に少量を均一に配合でき、ポリグリセリンエステル、ポ
リソルベートの食品品質改良効果が最大限に発揮出来る
1. Handling of polyglycerin esters and polysorbates becomes extremely easy, and in particular, small amounts can be uniformly blended into powdered foods or food raw materials, and the food quality improvement effects of polyglycerin esters and polysorbates can be maximized.

2.製造工程おいて、粉末で添加するのが望ましい食品
ないし食品原料へのポリグリセリンエステル、ポリソル
ベートの添加が容易になり、作業性が向上する。
2. In the manufacturing process, polyglycerin esters and polysorbates can be easily added to foods or food raw materials, which are preferably added in the form of powder, and workability is improved.

3.ポリグリセリンエステル、ポリソルベートが粉末ジ
ュースや粉末ドレッシングなど酸性粉末食品に添加しや
すくなる。
3. Polyglycerin esters and polysorbates can be easily added to acidic powdered foods such as powdered juices and powdered dressings.

Claims (2)

【特許請求の範囲】[Claims] (1)ポリグリセリン脂肪酸エステル及び/又はポリオ
キシエチレン(20)ソルビタン脂肪エステル100重
量部に対し、無水結晶マルトースを50〜500重量部
を加えて粉末化することを特徴とする粉末状乳化剤組成
物。
(1) A powdery emulsifier composition characterized by adding 50 to 500 parts by weight of anhydrous crystalline maltose to 100 parts by weight of polyglycerin fatty acid ester and/or polyoxyethylene (20) sorbitan fatty ester and pulverizing the mixture. .
(2)ポリグリセリン脂肪酸エステル及び/又はポリオ
キシエチレン(20)ソルビタン脂肪エステル100重
量部に対し、無水結晶マルトースを50〜500重量部
を加えて粉末化するに際し、水分を添加しないことを特
徴とする粉末状乳化剤組成物の製造法。
(2) When 50 to 500 parts by weight of anhydrous crystalline maltose is added to 100 parts by weight of polyglycerol fatty acid ester and/or polyoxyethylene (20) sorbitan fatty ester and powdered, no water is added. A method for producing a powdered emulsifier composition.
JP63064739A 1988-03-19 1988-03-19 Powdered emulsifier composition and its production Pending JPH01242133A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63064739A JPH01242133A (en) 1988-03-19 1988-03-19 Powdered emulsifier composition and its production

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63064739A JPH01242133A (en) 1988-03-19 1988-03-19 Powdered emulsifier composition and its production

Publications (1)

Publication Number Publication Date
JPH01242133A true JPH01242133A (en) 1989-09-27

Family

ID=13266821

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63064739A Pending JPH01242133A (en) 1988-03-19 1988-03-19 Powdered emulsifier composition and its production

Country Status (1)

Country Link
JP (1) JPH01242133A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004298848A (en) * 2003-04-01 2004-10-28 Mitsubishi Chemicals Corp Powdered emulsion stabilizer composition and producing method therefor
JP2009136282A (en) * 2007-11-16 2009-06-25 Kao Corp Powder composition for food

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004298848A (en) * 2003-04-01 2004-10-28 Mitsubishi Chemicals Corp Powdered emulsion stabilizer composition and producing method therefor
JP2009136282A (en) * 2007-11-16 2009-06-25 Kao Corp Powder composition for food

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