JPH07171377A - Manufacture of emulsified composition - Google Patents

Manufacture of emulsified composition

Info

Publication number
JPH07171377A
JPH07171377A JP5346218A JP34621893A JPH07171377A JP H07171377 A JPH07171377 A JP H07171377A JP 5346218 A JP5346218 A JP 5346218A JP 34621893 A JP34621893 A JP 34621893A JP H07171377 A JPH07171377 A JP H07171377A
Authority
JP
Japan
Prior art keywords
decaglycerin
acid ester
oil
emulsion
monooleate
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
JP5346218A
Other languages
Japanese (ja)
Inventor
Norihiko Inada
徳彦 稲田
Masayuki Nishino
雅之 西野
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
SANEI GEN F F I Inc
San Ei Gen FFI Inc
Original Assignee
SANEI GEN F F I Inc
San Ei Gen FFI Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=18381916&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=JPH07171377(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by SANEI GEN F F I Inc, San Ei Gen FFI Inc filed Critical SANEI GEN F F I Inc
Priority to JP5346218A priority Critical patent/JPH07171377A/en
Publication of JPH07171377A publication Critical patent/JPH07171377A/en
Pending legal-status Critical Current

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  • Fats And Perfumes (AREA)
  • General Preparation And Processing Of Foods (AREA)
  • Medicinal Preparation (AREA)
  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
  • Colloid Chemistry (AREA)

Abstract

PURPOSE:To obtain an emulsifier which is stable for a long period of time and gives a flavor etc. by mixing decaglycerine monooleate, monoglyceride organic acid ester and/or enzyme-decomposed lecitin in the emulsification using decaglycerine mono-saturated aliphatic acid ester. CONSTITUTION:In the emulsification of oil in water or alcohol using dacaglycerine mono-saturated aliphatic acid ester, a mixture is used in which one or more kinds of compounds selected from 0.3-1.0 pt.wt. of decaglycerine monooleate, 0.002-0.1 pt.wt. of monoglyceride organic acid ester, and 0.001-0.1 pt.wt. of enzyme-decomposed lecitin are mixed with 1 pt.wt. of dacaglycerine mono-saturated aliphatic acid ester. This emulsifier does not cause a viscosity increase nor turn pasty with the passage of time.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は乳化組成物の製造方法に
関する。本発明の乳化組成物は食品、医薬品、化粧品、
ペットフード、医薬部外品等に長期間安定で望ましい香
気、色調、濁度を付与するのに使用される。
FIELD OF THE INVENTION The present invention relates to a method for producing an emulsion composition. The emulsion composition of the present invention is a food, a drug, a cosmetic,
It is used for pet food, quasi-drugs, etc. to impart a desirable aroma, color tone and turbidity for a long period of time.

【0002】[0002]

【従来の技術】従来の乳化組成物としては精油類、油溶
性色素類、動植物性油脂類のような油性物質をペクチ
ン、アラビアガムなどの植物性天然ガム質および比重調
整剤で乳化したものが用いられていた。しかしながら使
用する天然ガム質は天候、気温などの自然環境によって
その生産量や品質が一定せず、価格の高騰や品質のバラ
ツキなどの問題があった。そこでこの欠点を解消するも
のとして、天然ガム質の代わりにポリグリセリン脂肪酸
エステルを使用して乳化組成物を得る方法が提案されて
いる(特開昭62−215343号、同2−53455
号および特公平5−27376号)。しかしながらこれ
らの提案においては乳化組成物の酸性飲料や食品に対す
る長期乳化安定性については言及しているが、乳化組成
物の経時的な粘度増加やペースト化を防止する技術課題
に関しては全く言及も示唆もしていない。
2. Description of the Related Art Conventional emulsified compositions include those obtained by emulsifying oily substances such as essential oils, oil-soluble pigments, animal and vegetable oils and fats with natural botanical gums such as pectin and gum arabic and a specific gravity adjusting agent. Was used. However, the amount and quality of the natural gums used are not constant depending on the natural environment such as weather and temperature, and there are problems such as soaring prices and variations in quality. Therefore, as a solution to this drawback, there has been proposed a method of obtaining an emulsified composition by using a polyglycerin fatty acid ester instead of a natural gum (Japanese Patent Laid-Open Nos. 62-215343 and 2-53455).
And Japanese Examined Patent Publication No. 5-27376). However, although these proposals refer to the long-term emulsion stability of the emulsified composition for acidic beverages and foods, they also suggest at all the technical problems of preventing the viscosity increase and pasting of the emulsified composition over time. I haven't.

【0003】ポリグリセリン脂肪酸エステルの中でもデ
カグリセリンモノ飽和脂肪酸エステルは香味の面で脂肪
酸臭が少なく、酸性下での長期乳化安定性の優れたもの
として知られており、利用価値の非常に高い界面活性剤
である。しかしながらデカグリセリンモノ飽和脂肪酸エ
ステルを用いて油性物質を水や多価アルコール中に乳化
させた組成物は、長期間乳化安定性に対して効果的とな
る2%(重量以下同じ)以上を添加すると、経時的に粘
度増加又はペースト化を生じ、使用の際のハンドリング
を著しく損なうものであった。また、ペースト化を生じ
ると最終飲食品に添加した場合、乳化組成物の分散性が
著しく低下し、商品価値を失う恐れがある。特に乳化組
成物中に占める油性物質の割合が20%を越える場合
は、この傾向が顕著に発現し、問題となっていた。
Among polyglycerin fatty acid esters, decaglycerin monosaturated fatty acid ester is known to have little fatty acid odor in terms of flavor and excellent in long-term emulsion stability under acidic conditions, and thus has a very high utility value. It is an activator. However, a composition obtained by emulsifying an oily substance in water or a polyhydric alcohol using decaglycerin monosaturated fatty acid ester is effective for long-term emulsification stability when 2% (same as below by weight) or more is added. However, the viscosity increased or formed into a paste with the passage of time, and the handling during use was significantly impaired. Further, when the paste is formed, when added to the final food or drink, the dispersibility of the emulsified composition is significantly reduced, and the commercial value may be lost. In particular, when the proportion of the oily substance in the emulsified composition exceeds 20%, this tendency is remarkably exhibited, which is a problem.

【0004】[0004]

【発明が解決しようとする課題】上述の様に、デカグリ
セリンモノ飽和脂肪酸エステルを乳化剤として使用した
乳化組成物に於いては、乳化性や各種食品に対する乳化
安定性はもとより、それらの経時的な粘度増加又はペー
スト化を防止することが求められているが、現状では満
足できる状態ではなく、更に改善された乳化組成物の創
出は当業界の課題であった。
As described above, in an emulsified composition using a decaglycerin monosaturated fatty acid ester as an emulsifier, not only the emulsification property and the emulsion stability for various foods but Although it is required to prevent viscosity increase or paste formation, the present situation is not satisfactory, and the creation of a further improved emulsified composition has been a problem in the art.

【0005】[0005]

【課題を解決するための手段】本発明は、デカグリセリ
ンモノ飽和脂肪酸エステルを用いて油性物質を水や多価
アルコール中に乳化させる時、デカグリセリンモノオレ
ート、モノグリセリド有機酸エステル及び酵素分解レシ
チンの内から選ばれた1種または2種以上の混合物を配
合することにより、従来のデカグリセリンモノ飽和脂肪
酸エステルの優れた効果を損なうことなく、経時的な粘
度増加もしくはペースト化を生じえない乳化組成物を得
ることによる。これらのペースト化防止に有効な配合割
合は、デカグリセリンモノ飽和脂肪酸エステルが1部
(重量以下同じ)に対し、デカグリセリンモノオレート
0.3〜1.0部、モノグリセリド有機酸エステル0.
002〜0.1部、酵素分解レシチン0.001〜0.
1部の割合が最も望ましい。このような乳化剤混合物を
乳化組成物に対して3〜10%、好ましくは4〜7%含
有させる。
Means for Solving the Problems The present invention provides a method of emulsifying an oily substance in water or a polyhydric alcohol using a decaglycerin monosaturated fatty acid ester, which comprises decaglycerin monooleate, a monoglyceride organic acid ester and an enzymatically decomposed lecithin An emulsified composition that does not cause an increase in viscosity or a paste formation with time without impairing the excellent effect of the conventional decaglycerin monosaturated fatty acid ester by blending one kind or a mixture of two or more kinds selected from the above. By getting things. The compounding ratio effective for preventing the formation of paste is 0.3 to 1.0 part of decaglycerin monooleate to 0.1 part of decaglycerin monosaturated fatty acid ester and 1 part of decaglycerin monosaturated fatty acid ester and monoglyceride organic acid ester.
002-0.1 parts, enzymatically decomposed lecithin 0.001-0.
A ratio of 1 part is most desirable. Such an emulsifier mixture is contained in the emulsified composition in an amount of 3 to 10%, preferably 4 to 7%.

【0006】本発明に利用することのできるデカグリセ
リンモノ飽和脂肪酸エステルとしてはHLBが10以上
のデカグリセリンモノステアレート、デカグリセリンモ
ノパルミテートおよびそれらの混合物を例示することが
できる。本発明に利用することのできるデカグリセリン
モノオレートはHLB10以上、好ましくは12以上の
ものを用いる。また、本発明に利用することのできるモ
ノグリセリド有機酸エステルとしては、例えば、コハク
酸モノグリセリド、クエン酸モノグリセリド、酢酸モノ
グリセリド、乳酸モノグリセリド、ジアセチル酒石酸モ
ノグリセリド等を例示することができる。更に、本発明
に利用することのできる酵素分解レシチンとしては、大
豆より抽出した高純度の分画レシチンを、フォスホリパ
ーゼA2を用いて部分加水分解したリゾレシチンなどが
挙げられる。
Examples of the decaglycerin monosaturated fatty acid ester that can be used in the present invention include decaglycerin monostearate having a HLB of 10 or more, decaglycerin monopalmitate, and mixtures thereof. The decaglycerin monooleate that can be used in the present invention has a HLB of 10 or more, preferably 12 or more. Examples of the monoglyceride organic acid ester that can be used in the present invention include succinic acid monoglyceride, citric acid monoglyceride, acetic acid monoglyceride, lactic acid monoglyceride, diacetyltartaric acid monoglyceride and the like. Further, examples of the enzyme-decomposed lecithin that can be used in the present invention include lysolecithin obtained by partially hydrolyzing a highly pure fractionated lecithin extracted from soybean with phospholipase A 2 .

【0007】本発明で用いる油性物質としては、例えば
オレンジ、ライム、レモン、グレープフルーツなどの柑
橘類精油、ペパーミントオイル、シソオイル、などのス
パイス類の精油、ペパー、シンナモン、ジンジャーなど
のオレオレジン、ジャスミン、ローズなどのアブソリュ
ート、および合成香料化合物、油性調合香料組成物およ
びこれらの任意の混合物の如き油性の着香料、パーム油
カロチン、ドナリエラカロチン、ニンジンカロチン等の
天然カロチン、および合成のβ−カロチン、パプリカ色
素、アナトー色素、リコペンおよびクロロフィルなどの
油溶性天然色素類、更に肝油、ビタミンA、ビタミン
D、ビタミンB2酪酸エステル、天然ビタミンE混合物
などの脂溶性ビタミン類、大豆油、菜種油、コーン油、
オリーブ油、椰子油、サフラワー油、ひまわり油、米
油、牛脂、豚脂、魚油などの動植物油脂、ドコサヘキサ
エン酸、エイコサペンタエン酸、γ−リノレン酸などの
天然高度不飽和脂肪酸類、シュークロースジアセテート
ヘキサイソブチレート(以下SAIBという)、C6
12の中鎖飽和脂肪酸トリグリセライドなどの加工食用
油脂およびこれら可食性油性材料の任意の混合物を例示
することができる。
Examples of the oily substance used in the present invention include essential oils of citrus fruits such as orange, lime, lemon and grapefruit, essential oils of spices such as peppermint oil and perilla oil, oleoresin such as pepper, cinnamon and ginger, jasmine and rose. Absolute and synthetic perfume compounds, oil-based flavoring agents such as oil-based fragrance compositions and any mixtures thereof, natural carotene such as palm oil carotene, donaliera carotene, carrot carotene, and synthetic β-carotene, paprika pigment. , Oil-soluble natural pigments such as annatto pigment, lycopene and chlorophyll, and fat-soluble vitamins such as liver oil, vitamin A, vitamin D, vitamin B 2 butyrate, natural vitamin E mixture, soybean oil, rapeseed oil, corn oil,
Olive oil, coconut oil, safflower oil, sunflower oil, rice oil, beef tallow, lard, fish oil and other animal and vegetable oils, docosahexaenoic acid, eicosapentaenoic acid, γ-linolenic acid and other highly unsaturated fatty acids, sucrose diacetate Hexaisobutyrate (hereinafter referred to as SAIB), C 6 ~
Processed edible oils and fats such as C 12 medium chain saturated fatty acid triglycerides and any mixture of these edible oily materials may be mentioned.

【0008】本発明で利用することのできる多価アルコ
ール類としては例えばグリセリン、プロピレングリコー
ル、ソルビトール、マルチトール、澱粉分解還元物、グ
ルコース、蔗糖、マルトースなどおよびこれらの2種以
上の混合物を例示することができる。これらの多価アル
コールの含水率は5〜40%であることが望ましく、こ
のような多価アルコール類を乳化組成物に対して50〜
87%使用する。以下実施例を示して本発明を更に具体
的に説明する。
Examples of the polyhydric alcohols that can be used in the present invention include glycerin, propylene glycol, sorbitol, maltitol, starch degradation products, glucose, sucrose, maltose and the like, and mixtures of two or more thereof. be able to. The water content of these polyhydric alcohols is preferably 5 to 40%, and such polyhydric alcohols are added to the emulsified composition in an amount of 50 to 50%.
Use 87%. Hereinafter, the present invention will be described more specifically with reference to Examples.

【0009】[0009]

【実施例】【Example】

実施例1 β−カロチン5g、SAIB14g、天然ビタミンE
0.5g、精製椰子油7g、大豆レシチン0.5gの混
合物を約150℃に加熱して、均一な油性材料混合物を
得た。別にグリセリン55g、水12gの混合物にデカ
グリセリンモノステアレート(HLB13)4gとデカ
グリセリンモノオレート(HLB12)2gを溶解した
溶液を得、前述の油性材料混合物の全量を加えて予備撹
拌させ、分散させた後、ホモジナイザーにて乳化し、油
脂の粒子約0.4μmの均一な着色剤乳化物(本発明品
No.1)を得た。
Example 1 β-carotene 5 g, SAIB 14 g, natural vitamin E
A mixture of 0.5 g, refined coconut oil 7 g and soybean lecithin 0.5 g was heated to about 150 ° C. to obtain a uniform oily material mixture. Separately, a solution of 4 g of decaglycerin monostearate (HLB13) and 2 g of decaglycerin monooleate (HLB12) dissolved in a mixture of 55 g of glycerin and 12 g of water was obtained, and the whole amount of the oily material mixture was added and pre-stirred to disperse. After that, the mixture was emulsified with a homogenizer to obtain a uniform colorant emulsion (invention product No. 1) having oil and fat particles of about 0.4 μm.

【0010】実施例2 実施例1においてデカグリセリンモノステアレートの添
加量を5.97gとし、デカグリセリンモノオレート2
gの代わりにコハク酸モノグリセリド0.03gを添加
した他は実施例1と同様の条件によって油脂の粒子約
0.4μmの均一な着色剤乳化物(本発明品No.2)
を得た。
Example 2 The amount of decaglycerin monostearate added in Example 1 was 5.97 g, and decaglycerin monooleate 2 was added.
A uniform colorant emulsion of particles of oil and fat of about 0.4 μm (invention product No. 2) under the same conditions as in Example 1 except that 0.03 g of succinic acid monoglyceride was added instead of g.
Got

【0011】実施例3 実施例1においてデカグリセリンモノステアレートの添
加量を5.5gとし、デカグリセリンモノオレート2g
の代わりに酵素分解レシチン0.5gを添加した他は実
施例1と同様の条件によって油脂の粒子約0.4μmの
均一な着色剤乳化物(本発明品No.3)を得た。
Example 3 The amount of decaglycerin monostearate added in Example 1 was set to 5.5 g, and 2 g of decaglycerin monooleate was added.
In the same manner as in Example 1 except that 0.5 g of enzymatically decomposed lecithin was added, a uniform colorant emulsion (particles of the present invention No. 3) having oil and fat particles of about 0.4 μm was obtained.

【0012】実施例4 レモンオイル3g、SAIB8.9g、天然ビタミンE
0.1g、中鎖飽和脂肪酸トリグリセライド8.5gを
溶解して、均一な油性材料混合物を得た。別にグリセリ
ン52g、水25gの混合物にデカグリセリンモノパル
ミテート(HLB13)4.5gとデカグリセリンモノ
オレート(HLB12)1.5gの混合物4gを溶解し
た溶液を得、前述の油性材料混合物の全量を加えて予備
撹拌させ、分散させた後、ホモジナイザーにて乳化し、
油脂の粒子約0.25μmの均一なレモン油乳化物(本
発明品No.4)を得た。
Example 4 Lemon oil 3 g, SAIB 8.9 g, natural vitamin E
0.1 g and 8.5 g of medium-chain saturated fatty acid triglyceride were dissolved to obtain a uniform oily material mixture. Separately, a solution in which 4 g of a mixture of 4.5 g of decaglycerin monopalmitate (HLB13) and 1.5 g of decaglycerin monooleate (HLB12) was dissolved in a mixture of 52 g of glycerin and 25 g of water was added, and the whole amount of the oily material mixture was added. After pre-stirring and dispersing, emulsify with a homogenizer,
A uniform lemon oil emulsion (invention product No. 4) having fat and oil particles of about 0.25 μm was obtained.

【0013】実施例5 実施例1においてデカグリセリンモノパルミテートの添
加量を5.99gとし、デカグリセリンモノオレート2
gの代わりにクエン酸モノグリセリド0.01gを添加
した他は実施例1と同様の条件によって油脂の粒子約
0.25μmの均一な均一なレモン油乳化物(本発明品
No.5)を得た。
Example 5 The amount of decaglycerin monopalmitate added in Example 1 was 5.99 g, and decaglycerin monooleate 2 was added.
In the same manner as in Example 1 except that 0.01 g of citric acid monoglyceride was added instead of g, a uniform and uniform lemon oil emulsion having oil and fat particles of about 0.25 μm (invention product No. 5) was obtained. .

【0014】実施例6 実施例1においてデカグリセリンモノパルミテートの添
加量を5.7gとし、デカグリセリンモノオレート2g
の代わりに酵素分解レシチン0.3gを添加した他は実
施例1と同様の条件によって油脂の粒子約0.25μm
の均一なレモン油乳化物(本発明品No.6)を得た。
Example 6 The amount of decaglycerin monopalmitate added in Example 1 was 5.7 g, and 2 g of decaglycerin monooleate was used.
In the same manner as in Example 1 except that 0.3 g of enzyme-decomposed lecithin was added in place of the above, oil particles were about 0.25 μm.
To obtain a uniform emulsion of lemon oil (invention product No. 6).

【0015】対照例1 実施例1においてデカグリセリンモノオレートを使用せ
ず、その重量不足分をデカグリセリンモノステアレート
で補った他は実施例1と同じ条件によって着色剤乳化物
(対照品No.1)を得た。
Control Example 1 A colorant emulsion (control product No. 1) was prepared under the same conditions as in Example 1 except that decaglycerin monooleate was not used in Example 1 and the weight shortage was supplemented with decaglycerin monostearate. 1) was obtained.

【0016】対照例2 実施例1においてデカグリセリンモノオレートを使用せ
ず、その重量不足分をショ糖脂肪酸エステルで補った他
は実施例1と同じ条件によって着色剤乳化物(対照品N
o.2)を得た。
Control Example 2 A colorant emulsion (control product N) was prepared under the same conditions as in Example 1 except that decaglycerin monooleate was not used in Example 1 and the weight shortage was supplemented with sucrose fatty acid ester.
o. 2) was obtained.

【0017】対照例3 実施例1においてデカグリセリンモノオレートを使用せ
ず、その重量不足分をグリセリンで補った他は実施例1
と同じ条件によって着色剤乳化物(対照品No.3)を
得た。
Control Example 3 Example 1 was repeated except that decaglycerin monooleate was not used in Example 1 but the weight shortage was supplemented with glycerin.
A colorant emulsion (control product No. 3) was obtained under the same conditions as described above.

【0018】対照例4 実施例2においてコハク酸モノグリセリドを使用せず、
その重量不足分をクエン酸で補った他は実施例2と同じ
条件によって着色剤乳化物(対照品No.4)を得た。
Control Example 4 No succinic acid monoglyceride was used in Example 2,
A colorant emulsion (control product No. 4) was obtained under the same conditions as in Example 2 except that the insufficient weight was supplemented with citric acid.

【0019】対照例5 実施例3において酵素分解レシチンを使用せず、その重
量不足分をカゼインナトリウムで補った他は実施例3と
同じ条件によって着色剤乳化物(対照品No.5)を得
た。
Control Example 5 An emulsified colorant (control product No. 5) was obtained under the same conditions as in Example 3 except that the enzyme-decomposed lecithin was not used in Example 3 and the weight deficiency was supplemented with sodium caseinate. It was

【0020】対照例6 実施例3においてデカグリセリンモノステアレートの代
わりにヘキサグリセリンモノラウレート(HLB14)
を使用した他は実施例3と同じ条件によって着色剤乳化
物(対照品No.6)を得た。
Control Example 6 In Example 3, hexaglycerin monolaurate (HLB14) was used instead of decaglycerin monostearate.
A colorant emulsion (control product No. 6) was obtained under the same conditions as in Example 3 except that the above was used.

【0021】対照品7 実施例4においてデカグリセリンモノオレートを使用せ
ず、その重量不足分をデカグリセリンモノパルミテート
で補った他は実施例4と同じ条件によってレモン油乳化
物(対照品No.7)を得た。
Control product 7 Lemon oil emulsion (control product No. 4) was used under the same conditions as in Example 4 except that decaglycerin monooleate was not used in Example 4 and the weight shortage was supplemented with decaglycerin monopalmitate. 7) was obtained.

【0022】対照例8 実施例4においてデカグリセリンモノパルミテートを使
用せず、その重量不足分をデカグリセリンモノオレート
で補った他は実施例4と同じ条件によってレモン油乳化
物(対照品No.8)を得た。
Control Example 8 Lemon oil emulsion (control product No. 4) was used under the same conditions as in Example 4 except that decaglycerin monopalmitate was not used in Example 4 and the weight shortage was supplemented with decaglycerin monooleate. 8) was obtained.

【0023】対照例9 実施例4においてデカグリセリンモノパルミテートの代
わりにデカグリセリンモノカプレート(HLB16)を
使用した他は実施例4と同じ条件によってレモン油乳化
物(対照品No.9)を得た。
Control Example 9 A lemon oil emulsion (control product No. 9) was obtained under the same conditions as in Example 4 except that decaglycerin monocaprate (HLB16) was used instead of decaglycerin monopalmitate in Example 4. It was

【0024】対照例10 実施例4においてデカグリセリンモノパルミテートを使
用せず、その重量不足分をグリセリンで補った他は実施
例4と同じ条件によってレモン油乳化物(対照品No.
10)を得た。
Control Example 10 Lemon oil emulsion (control product No. 4) was used under the same conditions as in Example 4 except that decaglycerin monopalmitate was not used in Example 4 and the insufficient weight was supplemented with glycerin.
10) was obtained.

【0025】比較実験1 実施例1〜3および対照例1〜6の着色剤乳化物(本発
明品No.1〜3および対照品1〜6)を同一日に調製
し、これらをサンプル瓶に充填して乳化物の粘度につい
て経時的に状態観察を行った。また、同時にグラニュー
糖130g、クエン酸4g、ビタミンC0.25gを適
量の水に溶解し、クエン酸ナトリウムを用いてpH3.
0に調製した後、全体を1lとして酸性飲料用シロップ
を調製した。このシロップ各200mlに実施例1〜3
および対照例1〜6で得られた乳化物の10%水溶液を
2ml添加し、瓶に充填後打栓し、85℃にて30分殺
菌後冷却して、着色飲料を得た。これを室温で静置し、
経時変化を観察した。結果を表1に示す。
Comparative Experiment 1 Colorant emulsions of Examples 1 to 3 and Control Examples 1 to 6 (invention products Nos. 1 to 3 and control products 1 to 6) were prepared on the same day, and these were placed in sample bottles. The state of the viscosity of the emulsion after filling was observed over time. At the same time, 130 g of granulated sugar, 4 g of citric acid, and 0.25 g of vitamin C were dissolved in an appropriate amount of water, and sodium citrate was used to adjust the pH to 3.
After adjusting to 0, the whole was made into 1 l and the syrup for acidic drinks was prepared. Examples 1-3 for each 200 ml of this syrup
Then, 2 ml of a 10% aqueous solution of the emulsion obtained in each of Control Examples 1 to 6 was added, the bottle was filled and capped, sterilized at 85 ° C. for 30 minutes and then cooled to obtain a colored beverage. Let it stand at room temperature,
The change with time was observed. The results are shown in Table 1.

【0026】[0026]

【表1】 [Table 1]

【0027】表中の各記号は下記の意味を表す。 粘度 ◎:流動性が高く、ペースト化の兆候は全く認められな
い。 ○:僅かに粘度は高いが、ペースト化は認められない。 △:流動性が低く、ペースト化の兆候が認められる。 ×:流動性が無く、ペースト化を生じている。 ネックリング −:ネックリングの発生は認められない。 ±:ネックリングを僅かに認める。 +:明瞭なネックリングを認める。 ++:著しいネックリングを認める。
Each symbol in the table has the following meaning. Viscosity ⊚: High fluidity, no sign of paste formation is observed. ◯: Viscosity is slightly high, but paste formation is not recognized. Δ: The fluidity is low and signs of paste formation are observed. X: There is no fluidity and a paste is formed. Neck ring-: No neck ring is observed. ±: A slight neck ring is recognized. +: A clear neck ring is recognized. ++: Remarkable neck ring is recognized.

【0028】表1の結果から明らかな通り、本発明品N
o.1〜3は3カ月後においても粘度増加もしくはペー
スト化を生じず、着色飲料におけるネックリングの発生
も認められなかったのに対し、対照品No.1、2、
4、5では経時的に粘度増加を起こし、2週間〜1カ月
後にはペースト化を生じた。また、対照品No.3、6
では粘度増加は認められなかったが、着色飲料におい
て、静置後1週間でネックリングの発生が認められ、約
3月後には著しいネックリングが生じ、商品価値を失っ
た。
As is clear from the results shown in Table 1, the product N of the present invention
o. Nos. 1 to 3 did not cause an increase in viscosity or formation of paste even after 3 months, and generation of neck ring in the colored beverage was not observed, whereas the control product No. 1, 2,
In Nos. 4 and 5, the viscosity increased with time, and after 2 weeks to 1 month, a paste was formed. The reference product No. 3, 6
Although no increase in viscosity was observed in the colored beverage, necking was observed in the colored beverage one week after standing, and marked necking occurred after about 3 months, resulting in loss of commercial value.

【0029】比較実験2 実施例4〜6および対照例7〜10のレモン油乳化物
(本発明品No.4〜6及び対照品No.7〜10)を
同一日に調製し、これらをサンプル瓶に充填して経時的
に状態観察を行った。また、同時にグラニュー糖120
g、クエン酸4g、を125gの水に溶解し、この溶液
に実施例4〜6および対照例7〜10で得られた乳化物
の10%水溶液を10ml添加し、炭酸水にて全体を1
lとした。瓶に充填後打栓し、炭酸飲料を得た。これを
室温で静置し、経時変化を観察した。結果を表2に示
す。
Comparative Experiment 2 Lemon oil emulsions of Examples 4 to 6 and Control Examples 7 to 10 (invention products Nos. 4 to 6 and control products No. 7 to 10) were prepared on the same day, and sampled. The bottle was filled and the condition was observed with time. At the same time, granulated sugar 120
g, 4 g of citric acid, was dissolved in 125 g of water, and 10 ml of a 10% aqueous solution of the emulsion obtained in Examples 4 to 6 and Comparative Examples 7 to 10 was added to this solution, and the whole was diluted with carbonated water to 1 g.
It was set to l. After filling the bottle, the bottle was stoppered to obtain a carbonated drink. This was left to stand at room temperature and the change with time was observed. The results are shown in Table 2.

【0030】[0030]

【表2】 [Table 2]

【0031】但し表中の各記号は表1と同じ。表2の結
果から明らかな通り、本発明品No.4〜6は3カ月後
においても粘度増加もしくはペースト化を生じず、炭酸
飲料でのネックリングの発生も認められなかったのに対
し、対照品No.7では経時的に粘度増加を起こし、1
カ月後にはペースト化を生じた。また、対照品No.8
〜10ではペースト化は生じなかったが、炭酸飲料にお
いて静置後1週間でネックリングの発生が認められ、3
月後には著しいネックリングを生じ、商品価値を失っ
た。
However, each symbol in the table is the same as in Table 1. As is clear from the results of Table 2, the product No. of the present invention. Nos. 4 to 6 did not cause an increase in viscosity or formation of paste even after 3 months, and generation of neck ring in carbonated beverages was not observed, whereas the control product No. In No. 7, viscosity increased with time, and
After a month, pasting occurred. The reference product No. 8
No paste formation occurred in Nos. 10 to 10, but necking was observed in a carbonated beverage one week after standing still.
After a month, it caused a remarkable neck ring and lost its commercial value.

【0032】比較実験3 実施例4〜6および対照例7〜10で得た乳化組成物そ
れぞれ約20gを容量50mlのサンプル瓶に入れ、6
0℃の恒温器内に4日間保存した後、レーザー回折式粒
度分布計SALD−1100((株)島津製作所)を用
いて粒子を測定した。その結果を表3に示す。
Comparative Experiment 3 Approximately 20 g of each of the emulsified compositions obtained in Examples 4 to 6 and Comparative Examples 7 to 10 was placed in a sample bottle having a volume of 50 ml, and 6
After storing in a thermostat at 0 ° C. for 4 days, particles were measured using a laser diffraction particle size distribution analyzer SALD-1100 (Shimadzu Corporation). The results are shown in Table 3.

【0033】[0033]

【表3】 [Table 3]

【0034】以上の結果から明らかな通り、対照品N
o.7〜10は60℃4日間の保存において粒子成長ま
たは粒子の凝集を起こすのに対して、本発明品No.4
〜6では粒子径に変化がなく安定であった。
As is clear from the above results, the control product N
o. Nos. 7 to 10 cause particle growth or particle aggregation during storage at 60 ° C. for 4 days, whereas the product No. 7 of the present invention. Four
In the case of ~ 6, there was no change in the particle size and it was stable.

【0035】[0035]

【発明の効果】本発明によって得られた乳化組成物は、
実施例の結果から明らかなように、粘度増加もしくはペ
ースト化を生じることなく、ハンドリングが極めて容易
であった。また、最終飲食品においても長期間にわたっ
て安定に分散し、好ましい濁度、色調、香味を保持し、
従来の天然ガム質を使用した乳化組成物に較べ、価格的
にも安価で、品質の面でも一定した製品が供給できるた
め、工業的意義は極めて大である。
The emulsified composition obtained by the present invention is
As is clear from the results of the examples, the handling was extremely easy without increasing the viscosity or forming a paste. Further, even in the final food or drink, it is stably dispersed over a long period of time, and retains a preferable turbidity, color tone and flavor,
Compared with conventional emulsified compositions using natural gums, it is industrially significant because it is cheaper in price and can provide products with consistent quality.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 B01F 17/44 // C11B 9/00 Z 2115−4H ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Office reference number FI technical display location B01F 17/44 // C11B 9/00 Z 2115-4H

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 デカグリセリンモノ飽和脂肪酸エステル
1重量部と以下に記載の〜の内から選ばれる1種ま
たは2種以上の混合物よりなる乳化剤を用いて乳化する
ことを特徴とする乳化組成物の製造方法。 0.3〜1.0重量部のデカグリセリンモノオレー
ト。 0.002〜0.1重量部のモノグリセリド有機酸エ
ステル。 0.001〜0.1重量部の酵素分解レシチン。
1. An emulsified composition characterized by emulsifying with 1 part by weight of decaglycerin monosaturated fatty acid ester and an emulsifier consisting of one or a mixture of two or more selected from the following: Production method. 0.3-1.0 parts by weight of decaglycerin monooleate. 0.002-0.1 parts by weight of monoglyceride organic acid ester. 0.001-0.1 parts by weight of enzymatically decomposed lecithin.
【請求項2】 デカグリセリンモノ飽和脂肪酸エステル
が、デカグリセリンモノステアレート及び又はデカグリ
セリンモノパルミテートであることを特徴とする請求項
1記載の乳化組成物の製造方法。
2. The method for producing an emulsion composition according to claim 1, wherein the decaglycerin monosaturated fatty acid ester is decaglycerin monostearate and / or decaglycerin monopalmitate.
JP5346218A 1993-12-20 1993-12-20 Manufacture of emulsified composition Pending JPH07171377A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5346218A JPH07171377A (en) 1993-12-20 1993-12-20 Manufacture of emulsified composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5346218A JPH07171377A (en) 1993-12-20 1993-12-20 Manufacture of emulsified composition

Publications (1)

Publication Number Publication Date
JPH07171377A true JPH07171377A (en) 1995-07-11

Family

ID=18381916

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5346218A Pending JPH07171377A (en) 1993-12-20 1993-12-20 Manufacture of emulsified composition

Country Status (1)

Country Link
JP (1) JPH07171377A (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005036206A (en) * 2003-06-26 2005-02-10 Mitsubishi Chemicals Corp Polyglycerol fatty acid ester and emulsified or solubilized composition containing the same
WO2005048742A1 (en) * 2003-11-14 2005-06-02 Eastman Chemical Company Sucrose acetate isobutyrate formulation
WO2006030850A1 (en) * 2004-09-15 2006-03-23 San-Ei Gen F.F.I., Inc. Method of preparing solution of lipid-soluble ingredient
JP2007267683A (en) * 2006-03-31 2007-10-18 Taiyo Kagaku Co Ltd Crowdy composition
JP2007267611A (en) * 2006-03-30 2007-10-18 Shiono Koryo Kk Spice composition, and food formulated with the same
CN100364498C (en) * 2003-04-03 2008-01-30 陈依军 Oral aerosol for reducing or eliminating snore and its preparation method
EP1927287A1 (en) 2006-12-01 2008-06-04 FUJIFILM Corporation Emulsion composition, and foods and cosmetics containing the emulsion composition
JP2008184385A (en) * 2007-01-26 2008-08-14 Ezaki Glico Co Ltd Dispersed hesperetin
JP2010030967A (en) * 2008-07-30 2010-02-12 Ezaki Glico Co Ltd Dispersed hesperetin
WO2023232392A1 (en) * 2022-05-30 2023-12-07 Firmenich Sa Flavor nanoemulsions for beverage and personal care applications

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100364498C (en) * 2003-04-03 2008-01-30 陈依军 Oral aerosol for reducing or eliminating snore and its preparation method
JP2005036206A (en) * 2003-06-26 2005-02-10 Mitsubishi Chemicals Corp Polyglycerol fatty acid ester and emulsified or solubilized composition containing the same
WO2005048742A1 (en) * 2003-11-14 2005-06-02 Eastman Chemical Company Sucrose acetate isobutyrate formulation
WO2006030850A1 (en) * 2004-09-15 2006-03-23 San-Ei Gen F.F.I., Inc. Method of preparing solution of lipid-soluble ingredient
JP2007267611A (en) * 2006-03-30 2007-10-18 Shiono Koryo Kk Spice composition, and food formulated with the same
JP4654356B2 (en) * 2006-03-30 2011-03-16 塩野香料株式会社 Fragrance composition and food containing the same
JP2007267683A (en) * 2006-03-31 2007-10-18 Taiyo Kagaku Co Ltd Crowdy composition
JP4660413B2 (en) * 2006-03-31 2011-03-30 太陽化学株式会社 Cloudy composition
EP1927287A1 (en) 2006-12-01 2008-06-04 FUJIFILM Corporation Emulsion composition, and foods and cosmetics containing the emulsion composition
JP2008184385A (en) * 2007-01-26 2008-08-14 Ezaki Glico Co Ltd Dispersed hesperetin
JP2010030967A (en) * 2008-07-30 2010-02-12 Ezaki Glico Co Ltd Dispersed hesperetin
WO2023232392A1 (en) * 2022-05-30 2023-12-07 Firmenich Sa Flavor nanoemulsions for beverage and personal care applications

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