JPS61260860A - Method of providing acidic drink with fragrance, color or turbidity - Google Patents

Method of providing acidic drink with fragrance, color or turbidity

Info

Publication number
JPS61260860A
JPS61260860A JP60101568A JP10156885A JPS61260860A JP S61260860 A JPS61260860 A JP S61260860A JP 60101568 A JP60101568 A JP 60101568A JP 10156885 A JP10156885 A JP 10156885A JP S61260860 A JPS61260860 A JP S61260860A
Authority
JP
Japan
Prior art keywords
oil
fatty acid
drink
acidic
turbidity
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.)
Granted
Application number
JP60101568A
Other languages
Japanese (ja)
Other versions
JPH0527376B2 (en
Inventor
Yoshiaki Chino
知野 善明
Shigeo Hatae
畑江 成郎
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.)
T Hasegawa Co Ltd
Original Assignee
T Hasegawa Co Ltd
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
Application filed by T Hasegawa Co Ltd filed Critical T Hasegawa Co Ltd
Priority to JP60101568A priority Critical patent/JPS61260860A/en
Publication of JPS61260860A publication Critical patent/JPS61260860A/en
Publication of JPH0527376B2 publication Critical patent/JPH0527376B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To provide an acidic drink with fragrance, color tone or turbidity stable for a long period, by blending an acidic drink with an emulsion composition of an oily ingredient prepared by using a polyglycerin fatty acid ester. CONSTITUTION:An acidic drink such a fruit drink, fermented milk drink, foamable refreshing drink, etc. is blended with about 0.02-2wt% emulsion composition obtained by blending at least one edible oily ingredient selected from a group consisting of an oil fragrant matter, an oil-soluble dyestuff, an animal or vegetable fat and oil, a middle chain fatty acid triglyceride, an oil- soluble vitamin and a vegetable natural resin with sucrose diacetate hexaisobutylate, a polyglycerin fatty acid ester having >=8 HLB and a polyhydric alcohol having <=50wt% water content.

Description

【発明の詳細な説明】 本発明は酸性飲料に長期間安定な香気、色調又杜混濁な
どの嗜好性の高い香味及び外観を与える方法に関し、更
に詳しくは、酸性飲料に(1)油性着香料、油溶性色素
類、動植物油脂類、中鎖飽和脂肪酸トリグリセラード類
、油溶性ビタミン類及び植物性天然樹脂よシなる群から
選ばれた少くとも1種の可食性油性材料(2)  シェ
ークロース・ジアセテート・ヘキサイソグチレート (
SAIB) (5)HLE  8以上のポリグリセリン脂肪酸エステ
ル類 (4)含水率50重量−以下の多価アルコール類からな
る組成物を酸性飲料に配合することを特徴とする酸性飲
料の着香、着色及び清濁方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for imparting a highly palatable flavor and appearance such as a long-term stable aroma, color tone, and turbidity to an acidic beverage. At least one edible oily material selected from the group consisting of , oil-soluble pigments, animal and vegetable oils, medium-chain saturated fatty acid triglycerides, oil-soluble vitamins, and vegetable natural resins (2) Diacetate hexaisobutyrate (
SAIB) (5) Polyglycerin fatty acid esters with HLE 8 or more (4) Flavoring and coloring of acidic beverages characterized by blending a composition consisting of polyhydric alcohols with water content of 50 weight or less into acidic beverages. and regarding the clarification method.

従来の技術 酸性飲料に好ましいフレーバー、混濁及び色調を付与す
る目的で、精油類、油浴性色X類、動植物油脂類などの
油性材料を添加しようとする飲料の糖濃度に合せて比重
調整した後、植物性天然ガム質、或いはショ糖脂肪酸エ
ステル、グリセリン脂肪酸エステルなどの食品用界面剤
を用いて乳化物を形成した後飲料に配合することは公知
である。
Conventional technology In order to impart a desirable flavor, turbidity, and color tone to acidic beverages, oil-based materials such as essential oils, oil bath color X, animal and vegetable oils and fats are added, and the specific gravity is adjusted according to the sugar concentration of the beverage. It is known to form an emulsion using a food-grade surfactant such as a vegetable natural gum or a sucrose fatty acid ester or a glycerin fatty acid ester, and then add the emulsion to a beverage.

しかしながら食品用界面活性の中で唯一、親水性で、高
HLBを有するショ糖脂肪酸エステルは酸性条件下にお
いては凝集現象がみられ、著しく安定性が劣υ、数ケ月
にも及ぶ混濁安定性を要求される酸性の飲料などへの利
用することは事実上不可能であり、この分野においては
高価なアラビアガムなどの天然植物がム質が専ら用いら
れている。
However, sucrose fatty acid ester, which is the only hydrophilic surfactant for food use and has a high HLB, shows aggregation phenomenon under acidic conditions and has extremely poor stability, resulting in turbidity lasting for several months. It is virtually impossible to use it for the required acidic beverages, and in this field, expensive natural plants such as gum arabic are used exclusively.

本発明者等は、香料、動植物油脂、油性色素などの油性
材料を水性乳化物として酸性飲料に配合するのに専ら用
いられてきた高価な天然植物がム質に代る界面活性剤を
用いた乳化組成物の利用を検討したところ、従来医薬品
、化粧品などに用いられていた/ リグリセリン脂肪酸
エステルを用いて製造された油性材料の乳化組成物が酸
性条件下でも極めて優れた安定性を長期間保持できるこ
とが分シ本発明を完成した。
The present inventors used a surfactant to replace the expensive natural plant-based mucilage that has been used exclusively to blend oily materials such as fragrances, animal and vegetable oils, and oil-based pigments into acidic beverages as aqueous emulsions. When we investigated the use of emulsified compositions, we found that emulsified compositions of oil-based materials manufactured using liglycerin fatty acid esters, which have been conventionally used in pharmaceuticals and cosmetics, have excellent stability for long periods even under acidic conditions. The present invention has been completed by being able to maintain this property.

ポリグリセリン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する方法は既に提案されている
(特開昭56−57040号公報Xしかしながらこの提
案においては得られた乳化組成物の水に対する分散性に
ついては言及しているが、これを酸性飲料に好ましい混
濁、色調及びフレーバーなどを賦与し、尚かつそれらの
好ましい香味、外観が数ケ月以上にも及ぶ長期間にわた
って安全に保持されることを要求される酸性飲料の技術
課題に関しては全く言及も示唆もしていない。
A method of emulsifying an oily substance in water or a polyhydric alcohol using a polyglycerin fatty acid ester has already been proposed (JP-A-56-57040). Although we are talking about dispersibility, it is important to use this to impart desirable turbidity, color tone, flavor, etc. to acidic beverages, and to maintain these desirable flavors and appearances safely for long periods of time, such as several months or more. There is no mention or suggestion of technical issues related to acidic beverages, which require the following.

本発明者等は、ポリグリセリン脂肪酸エステルを用いて
天然精油、油m性色素、着香料、動植物油脂、中鎖飽和
脂肪酸トリグリセラード、油m性ビタミン及び植物性天
然樹脂などの可食性油性材料を前記公知方法によって多
価アルコール中に乳化して得られた乳化物を水および酸
性飲料(Brig 12’、pH五〇)に0.1%添加
したところ、添加直後は好ましい混濁を呈したが翌日に
は油性成分が大部分表面に浮上し、混濁は著しく減少す
ることを認めた。
The present inventors used polyglycerol fatty acid esters to prepare edible oily materials such as natural essential oils, oily pigments, flavoring agents, animal and vegetable oils, medium-chain saturated fatty acid triglycerides, oily vitamins, and vegetable natural resins. When 0.1% of the emulsion obtained by emulsifying it in polyhydric alcohol by the above-mentioned known method was added to water and an acidic drink (Brig 12', pH 50), a favorable cloudiness was observed immediately after addition, but the result remained the same the next day. It was observed that most of the oily components rose to the surface and the turbidity was significantly reduced.

本発明者等は、従来提案の上記の如き重大欠点即ち、可
食性油性材料のポリグリセリン脂肪酸エステルによる乳
化組成物を、例えばpH約2〜約5の如き酸性領域にあ
り、且つ比重が1.0を超える酸性飲料に例えば約α0
2〜約2重量−の如き量を添加した場合にみられる乳化
粒子の分離浮上を防止すべく研究を行った。
The present inventors have solved the above-mentioned serious drawbacks of conventional proposals, namely, emulsified compositions made of polyglycerin fatty acid esters of edible oily materials, which have a pH in an acidic range of about 2 to about 5, and a specific gravity of 1. For example, about α0 for acidic beverages exceeding 0
Research was conducted to prevent the separation and flotation of emulsified particles that occurs when an amount of 2 to about 2 weight is added.

その結果、 (1)油性着香料、油溶性色素類、動植物油脂類、中鎖
飽和脂肪酸トリグリセラード類、油溶性ビタミン類及び
植物性天然樹脂よりなる群から選ばれた少くとも1種の
可食性油性材料(2)SAIE (5)HLE  8以上のポリグリセリン脂肪酸エステ
ル類 (4)含水率50重量−以下の多価アルコール類からな
る組成物を酸性飲料に配合することによって、前記従来
公知の乳化物の欠点を一挙に解決し、極めて好ましい香
味、混濁及び色調などが長期間にわたって保持される安
価な酸性飲料が得られることを見出した。
As a result, (1) at least one edible substance selected from the group consisting of oil-based flavorings, oil-soluble pigments, animal and vegetable oils, medium-chain saturated fatty acid triglycerides, oil-soluble vitamins, and vegetable natural resins; By blending a composition consisting of an oily material (2) SAIE (5) a polyglycerin fatty acid ester with an HLE of 8 or more (4) a polyhydric alcohol with a water content of 50 weight or less into an acidic beverage, the conventionally known emulsification can be achieved. It has been found that an inexpensive acidic beverage can be obtained which solves all the drawbacks of the product at once and retains extremely favorable flavor, turbidity, color tone, etc. for a long period of time.

本発明で用いる油性着香料の例としては、例えハ、オレ
ンジ、レモン、ライム、グレープフルーツなどの柑橘類
精油、花精油、ペパーミント油、スペアミント油、スパ
イス油などの植物精油;コーラナツツエキストラクト、
コーヒーエキストラクト、ワニラエキストラクト、ココ
アエキストラクト、紅茶エキストラクト、スパイス類エ
キストラクトなどの油性のエキストラクト及びこれらの
オレオレジン類;合成香料化合物、油性調合香料組成物
及びこれらの任意の混合物の如き油性の着香料;及びβ
−カロチン、パプリカ色素、アナトー色素及びクロロフ
ィルなどの油溶性天然色素類;肝油、ビタミンA1ビタ
ミンA油、ビタミンB。
Examples of oil-based flavoring agents used in the present invention include citrus essential oils such as orange, lemon, lime, and grapefruit; flower essential oils; plant essential oils such as peppermint oil, spearmint oil, and spice oil; cola nut extract;
Oil-based extracts such as coffee extract, wanilla extract, cocoa extract, black tea extract, spice extract and their oleoresins; synthetic fragrance compounds, oil-based blended fragrance compositions and any mixtures thereof. oil-based flavoring agents such as; and β
- Oil-soluble natural pigments such as carotene, paprika pigment, annatto pigment and chlorophyll; cod liver oil, vitamin A1 vitamin A oil, vitamin B.

酪酸エステル、天然ビタミンE混合物などの脂m性ビタ
ミン類;大豆油、ナタネ油、コーン油、オリーブ油、ヤ
シ油、サフラワー油、ヒマワリ油、米油、牛脂、豚油、
魚油などの動植物油脂類;ロジン、コーパル、ダンマル
、エレミ、エステルガムなどの植物性樹脂類;C・〜C
8!の中鎖飽和脂肪酸トリグリセラードなどの加工食用
油脂及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。
Fatty vitamins such as butyrate ester, natural vitamin E mixture; soybean oil, rapeseed oil, corn oil, olive oil, coconut oil, safflower oil, sunflower oil, rice oil, beef tallow, pork oil,
Animal and vegetable fats and oils such as fish oil; Vegetable resins such as rosin, copal, dammar, elemi, and ester gum; C・~C
8! Examples include processed edible fats and oils such as medium-chain saturated fatty acid triglycerides, and any mixtures of these edible oily materials.

また本発明で利用することのできるポリグリセリン脂肪
酸エステル類としては、例えば平均重合度3以上のポリ
グリセリンと炭素数8以上の脂肪酸とのエステルでかつ
、HLBが8以上、好ましくはHLBが10以上のもの
を例示することができる。
Further, the polyglycerin fatty acid esters that can be used in the present invention include, for example, an ester of polyglycerin with an average degree of polymerization of 3 or more and a fatty acid having 8 or more carbon atoms, and an HLB of 8 or more, preferably an HLB of 10 or more. The following can be exemplified.

更に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、ンル
ビトール、マルチトール、a粉分j% R元’all 
、グルコース、ショ糖、マルトースナトの糖類及びこれ
らの二種以上の混合物を例示することができる。
Furthermore, examples of polyhydric alcohols that can be used in the present invention include glycerin, propylene glycol, nlubitol, maltitol, powder content j%
, glucose, sucrose, maltose, and mixtures of two or more thereof.

次に本発明の好ましい一実施態様を例示すれば、先ず前
記した如き可食性油性材料と5AIBを混合し、例えば
室温乃至約180℃に加熱爵解して均一混合油とする。
Next, to illustrate a preferred embodiment of the present invention, first, the above-described edible oily material and 5AIB are mixed and heated to, for example, room temperature to about 180° C. to form a uniformly mixed oil.

かかる可食性油性材料と5AIHの混合割合は、乳化後
の組成物を添加しようとする酸性飲料の比重に合致する
ように配合すれば良い。
The mixing ratio of the edible oily material and 5AIH may be adjusted to match the specific gravity of the acidic beverage to which the emulsified composition is added.

かくして得られた油性材料混合物1重量部を、例えば水
分含有量約0〜約50重量%の多価アルコールに約1]
、5〜約10重量%のポリグリセリン脂肪酸エステルを
混合爵解した多価アルコール啓液約2〜約50重量部と
混合し、ホモミキサー、コロイドミル高圧ホモジナイザ
ー等を用いて乳化処理することによシ、粒子径約0.2
〜約1ミクロンの極めて微細で安定性の優れた乳化液を
得ることができる。所望によシ多価アルコール溶液にポ
リグリセリンに加えて例えばショ糖脂肪酸エステル、ソ
ルビタン脂肪酸エステルなどの親水性界面活性剤、アラ
ビアがA、)ラガントガム、キサンタンガム、CMCな
どの天然及び合成糊料或いはゼラチン、カゼインなどの
蛋白質、更には、保存性を向上させる目的で乳酸、リン
ゴ酸、クエン酸、酒石酸などの有機酸を添加することも
できる。また一方、前記油性材料混合物には所望によシ
、グリセリン脂肪酸エステル及びレシチンの如き親油性
の乳化剤を添加配合することもできる。
One part by weight of the oily material mixture thus obtained is mixed with, for example, a polyhydric alcohol having a water content of about 0 to about 50% by weight.
, 5 to about 10% by weight of polyglycerol fatty acid ester is mixed with about 2 to about 50 parts by weight of a mixed polyhydric alcohol solution, and the mixture is emulsified using a homomixer, a colloid mill high-pressure homogenizer, etc. Particle size: approx. 0.2
An extremely fine emulsion of ~1 micron and excellent stability can be obtained. If desired, in addition to polyglycerin in a polyhydric alcohol solution, hydrophilic surfactants such as sucrose fatty acid ester and sorbitan fatty acid ester, a) natural and synthetic thickeners such as arabic gum, xanthan gum, and CMC, or gelatin. , proteins such as casein, and organic acids such as lactic acid, malic acid, citric acid, and tartaric acid may also be added for the purpose of improving storage stability. On the other hand, if desired, a lipophilic emulsifier such as glycerin fatty acid ester and lecithin may be added to the oily material mixture.

本発明は上記の如くして得られた組成物を酸性飲料例え
ば果汁飲料、醗酵乳飲料、発泡性清涼飲料などに例えば
約102〜約2重量%配合するととKよって該飲料に長
期間安定で好ましい香味、色調及び混濁を賦与ないし増
強することができる。
According to the present invention, when the composition obtained as described above is blended into an acidic drink such as a fruit juice drink, a fermented milk drink, a sparkling soft drink, etc. in an amount of, for example, about 102 to about 2% by weight, the composition is stable for a long period of time in the drink. Desirable flavor, color and turbidity can be imparted or enhanced.

以下実施例によって本発明の数態様を更に詳しく説明す
る。
Hereinafter, several aspects of the present invention will be explained in more detail with reference to Examples.

参考例1 β−カロチン8g、ロジン10g、リモネン1(1,5
AIBS6.7ys天然ビタミンE CL5グ及び精製
ヤシ油14.8gの混合物を窒素気流中で約160℃に
加温して、均一な油性材料混合物Cfo 1.048)
を得た。この混合物を70%ソルビトール890gにデ
カグリセリンモノステアレート10gを溶解した溶液に
加えて予備攪拌して分散させた後、TK−ホモミキサー
にて5000デpmにて10分間乳化し、油脂の粒子約
1ミクロンの均一な酸性飲料用の着色剤乳化組成物を得
た(本発明品I&1)。
Reference example 1 β-carotene 8g, rosin 10g, limonene 1 (1,5
A mixture of AIBS6.7ys natural vitamin E CL5 and 14.8 g of refined coconut oil was heated to about 160°C in a nitrogen stream to form a homogeneous oily material mixture Cfo 1.048).
I got it. This mixture was added to a solution of 10 g of decaglycerol monostearate dissolved in 890 g of 70% sorbitol, preliminarily stirred and dispersed, and then emulsified for 10 minutes at 5,000 depm using a TK-Homo mixer. A colorant emulsion composition for acidic beverages with a uniform size of 1 micron was obtained (inventive product I & 1).

参考例2 オレンジオイル20g1精製ダンマルガム20g、 S
AI B 47.4 Qz ’a〜C1!ミルC1!飽
和脂肪酸トリグリセラード、617を混合爵解して、d
tol、04131C比重調整したオレンジ油混合物を
得た。
Reference example 2 20 g of orange oil 1 20 g of purified dammar gum, S
AI B 47.4 Qz 'a~C1! Mil C1! Mixed oxidation of saturated fatty acid triglyceride, 617, d
An orange oil mixture with adjusted specific gravity of tol and 04131C was obtained.

別にグリセリン500g、水370gの混合物にヘキサ
グリセリンモノオレエー)10gを廖解し、更に50%
乳酸2017を加えて均一な溶液を得、先に調製したオ
レンジ油混合物の全量を加えて、予備乳化した後、TK
−ホモミキサーにて5゜00Orpm、10分間乳化処
理を行い、酸性飲料用オレンジ油乳化物を得た(本発明
品遥2)。
Separately, 10g of hexaglycerin monooleate was dissolved in a mixture of 500g of glycerin and 370g of water, and further 50%
Add lactic acid 2017 to obtain a homogeneous solution, add the entire amount of the orange oil mixture prepared earlier to pre-emulsify, and then add TK.
- Emulsification was carried out using a homomixer at 5°00 rpm for 10 minutes to obtain an orange oil emulsion for acidic beverages (product of the present invention Haruka 2).

参考例3 ビタミンE30Q、5AIB6’2.7Q、中鎖飽和脂
肪酸トリグリセラード混合物(カプリル酸75s1カプ
リン酸25チ)7.5 yを混合爵解してd!o1.0
61の比重調整されたビタミンE油混合物100gを得
喪。別にグリセリン500g。
Reference Example 3 Vitamin E30Q, 5AIB6'2.7Q, medium chain saturated fatty acid triglyceride mixture (caprylic acid 75s1 capric acid 25t) 7.5y were mixed and d! o1.0
Obtain 100 g of vitamin E oil mixture with adjusted specific gravity of 61. Separately 500g of glycerin.

水570yの混合物にヘキサグリセリンモノオレエート
10g及び50%乳酸20yを加えて均一な溶液とした
ところへ、前記ビタミンE油混合物の全量を加え、予備
乳化した後、TK−ホモミキサーニて500Orpmに
て10分間乳化処理し、酸性健康飲料用ビタミンE油乳
化物を得たC本発明品A3)。
To a mixture of 570 y of water, 10 g of hexaglycerin monooleate and 20 y of 50% lactic acid were added to make a homogeneous solution, then the entire amount of the vitamin E oil mixture was added and pre-emulsified, and then a TK-Homo mixer was heated at 500 rpm for 10 min. Inventive product A3) obtained by emulsifying for a minute to obtain a vitamin E oil emulsion for acidic health drinks.

比較例1 参考例1においてデカグリセリンモノステアレートにか
えてショ糖脂肪酸エステル(HLB15)10gを使用
したほかは、参考例1と同じ条件によって、着色剤乳化
物を得た(比較品ム1)。
Comparative Example 1 A colorant emulsion was obtained under the same conditions as in Reference Example 1, except that 10 g of sucrose fatty acid ester (HLB15) was used in place of decaglycerol monostearate in Reference Example 1 (Comparative Product M1). .

比較例2 参考例2において、5AIBに代えてW製ヤシ油47.
40を混合したほかは参考例2と同一条件によってオレ
ンジ油乳化物を得た(比較品ム2)。
Comparative Example 2 In Reference Example 2, W coconut oil 47.
An orange oil emulsion was obtained under the same conditions as in Reference Example 2 except that No. 40 was mixed (Comparative Product M 2).

比較例3 参考例6において、ヘキサグリセリンモノオレエー)1
0gK代えて、ショ糖脂肪酸エステルCHLB13)1
0 Qとし九ほかは同一条件によって、ビタミンE油の
乳化物を得た(比較品45′)。
Comparative Example 3 In Reference Example 6, hexaglycerin monooleate) 1
In place of 0gK, sucrose fatty acid ester CHLB13)1
0 An emulsion of vitamin E oil was obtained under the same conditions as Q Toshiku and others (comparative product 45').

実施例1 グラニユー糖240 ysクエン酸8g及びビタミンC
05gを適量の水に溶解し、クエン酸ナトリウムを用い
てpH5,OI/C’U4整した後、全体を26として
酸性飲料用シロップを調整した。このシロップ各200
−に参考例1及び比較例1で得られた乳化物をそれぞれ
α2−を添加し、ビンに充填後打栓し、85℃にて15
分殺菌後冷却し、好ましい黄色に着色された飲料を得た
。これを室温で保存し、経時変化を観察した。結果を第
1表に示す。
Example 1 Granulated sugar 240ys 8g of citric acid and vitamin C
After dissolving 05g in an appropriate amount of water and adjusting the pH to 5 and OI/C'U4 using sodium citrate, the total amount was adjusted to 26 to prepare a syrup for acidic beverages. This syrup 200 each
α2- was added to the emulsions obtained in Reference Example 1 and Comparative Example 1, respectively, and the bottles were filled and capped, and heated to 85°C for 15 minutes.
After sterilization for several minutes, the mixture was cooled to obtain a desirable yellow colored beverage. This was stored at room temperature and changes over time were observed. The results are shown in Table 1.

第1表 但し表中の各記号は下記の意味を表わす。Table 1 However, each symbol in the table represents the following meaning.

−ネックリングの発生は認められない。- No occurrence of neck ring is observed.

±  ネックリングを僅かに認める。± Neck ring is slightly visible.

+  明瞭なネックリングを認める。+ Clear neck ring is recognized.

+十  著しいネックリングを認める。+10 Noticeable neck ring.

+++ ネックリングが層状となる程激しくなる。+++ The more the neck ring becomes layered, the more intense it becomes.

第1表の結果から明らかな通り、本発明品ム1は、3t
月後においても全く安定であったのに対し、従来品は1
週間で著しいネックリングを発生した。
As is clear from the results in Table 1, the product M1 of the present invention has 3t
The conventional product remained completely stable even after 1 month, whereas the conventional product
Significant neck ring developed within a week.

実施例2 グラニュー!l11jOy、クエン酸2g及び温州みか
ん/、濃縮果汁20Qを水に溶解し、全量を1tとして
果汁10%の酸性飲料用シロップを調製した。このシロ
ップ各200mに参考例2 (本発明品ム2)及び比較
例2 (比較品ム2)で得られた乳化物をそれぞれCl
3−添加し、ピンに充填後打栓し、85℃にて15分間
殺菌後冷却してオレンジ果汁飲料を得た。これt−室温
に′f#置してネックリングの状態を観察した。結果を
第2表に示す。
Example 2 Granulated! 111jOy, 2 g of citric acid, Satsuma mandarin orange/20Q of concentrated fruit juice were dissolved in water, and the total amount was 1 t to prepare an acidic beverage syrup containing 10% fruit juice. The emulsions obtained in Reference Example 2 (Inventive Product M2) and Comparative Example 2 (Comparative Product M2) were added to each 200 m of this syrup using Cl.
3- was added, filled into a pin, capped, sterilized at 85° C. for 15 minutes, and then cooled to obtain an orange juice beverage. This was placed at room temperature and the condition of the neck ring was observed. The results are shown in Table 2.

第2表 但し、表中の記号は第1表と同じ意味を表わす。Table 2 However, the symbols in the table have the same meanings as in Table 1.

第2表の結果から明らかな通り、本発明品A2は3t月
後においても全く安定であったが、比較品A2は約1週
間でリングの発生が見られ、2週間後には著しいリング
となり、商品価値を失った。
As is clear from the results in Table 2, the product A2 of the present invention was completely stable even after 3 tons of months, but the comparative product A2 developed rings in about one week, and after two weeks, it became a noticeable ring. The product has lost its value.

実施例3 グラニュー糖145g、精製ハチミツ20g、ビタミン
C17にI、クエン酸1.5g、ニコチン酸アミド0.
5Q、  ビタミンBe  (塩酸ピリドキシン)α1
gs  ビタミンEx  (リボフラビンリン酸塩)a
、□sg、ビタミンP0.05g1天然カフェイン0.
29及びクエン酸ナトリウムQ、1gを水に溶解して全
量を1tとする。このシロップ各20011tに参考例
3(本発明品A3)及び比較例3 (比較品ム3)で得
られた乳化物をそれぞれcL211を添加し、がラスピ
ンに充填後、打栓し、85℃、15分殺菌後冷却し好ま
しい混濁のある栄養ドリンクを調製した。これを室温に
静置してネックリングの発生状況を観察した。結果を第
3表に示した。
Example 3 Granulated sugar 145g, refined honey 20g, vitamin C17 and I, citric acid 1.5g, nicotinamide 0.
5Q, Vitamin Be (pyridoxine hydrochloride) α1
gs Vitamin Ex (riboflavin phosphate) a
, □sg, vitamin P0.05g1 natural caffeine 0.
29 and sodium citrate Q, 1 g were dissolved in water to make a total amount of 1 t. To each 20,011 tons of this syrup, cL211 was added to each of the emulsions obtained in Reference Example 3 (Product A3 of the Invention) and Comparative Example 3 (Comparative Product M3), filled in a lath pin, capped, and heated at 85°C. After sterilization for 15 minutes and cooling, an nutritional drink with a desirable cloudiness was prepared. This was left at room temperature and the occurrence of neck ring was observed. The results are shown in Table 3.

第3表 但し表中の記号の意味は第1表と同じ。Table 3 However, the meanings of the symbols in the table are the same as in Table 1.

第3表の結果から明らかな通り、本発明品は3ケ月後に
おいても外観的変化は見られず全く安定であったのに対
し、比較品は、粒子が凝集して全体に濁りがなくなり、
表面に多量の浮遊物を生じた。
As is clear from the results in Table 3, the product of the present invention showed no change in appearance even after 3 months and was completely stable, whereas the comparative product had particles agglomerated and became completely cloudy.
A large amount of floating matter was formed on the surface.

発明の効果 本発明によって得られた酸性飲料用乳化組成物は、それ
自体極めて優れた保存安定性を有しており、更に該組成
物を例えば果汁飲料、乳酸菌飲料、発泡性飲料、栄養ド
リンクなどの酸性飲料に配合した場合には非常に好まし
い混濁性、色調及び香味を長期間にわたって保持し、該
飲料の嗜好性改善に極めて有用である。
Effects of the Invention The emulsified composition for acidic beverages obtained by the present invention itself has extremely excellent storage stability, and furthermore, the composition can be used for example in fruit juice drinks, lactic acid bacteria drinks, sparkling drinks, nutritional drinks, etc. When blended into acidic beverages, it retains very favorable turbidity, color tone, and flavor for a long period of time, and is extremely useful for improving the palatability of the beverage.

Claims (4)

【特許請求の範囲】[Claims] (1)油性着香料、油溶性色素類、動植物油脂類、中鎖
飽和脂肪酸トリグリセラード類、油溶性ビタミン類及び
植物性天然樹脂よりなる群から選ばれた少くとも、種の
可食性油性材料
(1) Edible oily material of at least seeds selected from the group consisting of oily flavorings, oil-soluble pigments, animal and vegetable oils, medium-chain saturated fatty acid triglycerides, oil-soluble vitamins, and vegetable natural resins.
(2)シュークローズ・ジアセテート・ヘキサイソブチ
レート(SAIB)
(2) Sucrose diacetate hexisobutyrate (SAIB)
(3)HLB8以上のポリグリセリン脂肪酸エステル類(3) Polyglycerin fatty acid esters with HLB 8 or higher (4)含水率50重量%以下の多価アルコール類からな
る組成物を酸性飲料に配合することを特徴とする酸性飲
料の着香、着色又は着濁方法。
(4) A method for flavoring, coloring, or clouding an acidic beverage, which comprises blending into the acidic beverage a composition comprising a polyhydric alcohol having a water content of 50% by weight or less.
JP60101568A 1985-05-15 1985-05-15 Method of providing acidic drink with fragrance, color or turbidity Granted JPS61260860A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60101568A JPS61260860A (en) 1985-05-15 1985-05-15 Method of providing acidic drink with fragrance, color or turbidity

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60101568A JPS61260860A (en) 1985-05-15 1985-05-15 Method of providing acidic drink with fragrance, color or turbidity

Publications (2)

Publication Number Publication Date
JPS61260860A true JPS61260860A (en) 1986-11-19
JPH0527376B2 JPH0527376B2 (en) 1993-04-21

Family

ID=14304009

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60101568A Granted JPS61260860A (en) 1985-05-15 1985-05-15 Method of providing acidic drink with fragrance, color or turbidity

Country Status (1)

Country Link
JP (1) JPS61260860A (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03277260A (en) * 1990-03-26 1991-12-09 Kanebo Ltd Drink filled in sealed container
JP2003003191A (en) * 2001-06-19 2003-01-08 T Hasegawa Co Ltd Flavor preparation with improved heat resistance and retention
EP1679063A1 (en) * 2003-10-10 2006-07-12 Eisai Co., Ltd. Novel liquid preparation composition
JP2007116931A (en) * 2005-10-26 2007-05-17 T Hasegawa Co Ltd Emulsified composition to be added to acidic beverage and method for producing the same
JP2009502930A (en) * 2005-07-26 2009-01-29 デュレクト コーポレーション Removal of peroxide from drug delivery vehicles
JP2009518027A (en) * 2005-12-09 2009-05-07 ダニスコ シュガー エイ/エス Stabilized emulsion
JP2009207383A (en) * 2008-03-03 2009-09-17 T Hasegawa Co Ltd Emulsion composition for coenzyme q10-containing beverage, and method for producing the same
US8168618B2 (en) 2006-01-19 2012-05-01 Kaneka Corporation Emulsifying agent
US8669287B2 (en) 2009-06-05 2014-03-11 Ajinomoto Co., Inc. Emulsifying preparation
US9119973B2 (en) 2008-12-30 2015-09-01 Takasago International Corporation Fragrance composition for core shell microcapsules
JP2021061866A (en) * 2021-01-26 2021-04-22 ハウスウェルネスフーズ株式会社 Folic acid-containing acidic composition having excellent stability of folic acid

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009095277A (en) * 2007-10-17 2009-05-07 Mitsubishi Chemicals Corp Method for producing beverage
JP6671094B2 (en) * 2014-07-07 2020-03-25 キリンビバレッジ株式会社 A clouded citrus juice-containing packaged beverage in which the precipitation of cloudy citrus juice is masked.

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4858169A (en) * 1971-11-22 1973-08-15
JPS5837040A (en) * 1981-08-28 1983-03-04 Ishikawajima Harima Heavy Ind Co Ltd Fire-retardant resin in concentrated oxygen
JPS58103325A (en) * 1981-12-10 1983-06-20 Sumitomo Chem Co Ltd Preparation of colored pharmaceutical dispersible easily in acidic solution

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4858169A (en) * 1971-11-22 1973-08-15
JPS5837040A (en) * 1981-08-28 1983-03-04 Ishikawajima Harima Heavy Ind Co Ltd Fire-retardant resin in concentrated oxygen
JPS58103325A (en) * 1981-12-10 1983-06-20 Sumitomo Chem Co Ltd Preparation of colored pharmaceutical dispersible easily in acidic solution

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03277260A (en) * 1990-03-26 1991-12-09 Kanebo Ltd Drink filled in sealed container
JP2003003191A (en) * 2001-06-19 2003-01-08 T Hasegawa Co Ltd Flavor preparation with improved heat resistance and retention
AU2004279225B2 (en) * 2003-10-10 2009-10-29 Mitsubishi-Chemical Foods Corporation Novel liquid preparation composition
EP1679063A1 (en) * 2003-10-10 2006-07-12 Eisai Co., Ltd. Novel liquid preparation composition
EP1679063A4 (en) * 2003-10-10 2007-02-28 Eisai R&D Man Co Ltd Novel liquid preparation composition
US8557259B2 (en) 2003-10-10 2013-10-15 Eisai R&D Management Co., Ltd. Liquid preparation
JP2009502930A (en) * 2005-07-26 2009-01-29 デュレクト コーポレーション Removal of peroxide from drug delivery vehicles
JP4512022B2 (en) * 2005-10-26 2010-07-28 長谷川香料株式会社 Method for producing emulsion composition for blending acidic beverage
JP2007116931A (en) * 2005-10-26 2007-05-17 T Hasegawa Co Ltd Emulsified composition to be added to acidic beverage and method for producing the same
JP2009518027A (en) * 2005-12-09 2009-05-07 ダニスコ シュガー エイ/エス Stabilized emulsion
US8168618B2 (en) 2006-01-19 2012-05-01 Kaneka Corporation Emulsifying agent
JP2009207383A (en) * 2008-03-03 2009-09-17 T Hasegawa Co Ltd Emulsion composition for coenzyme q10-containing beverage, and method for producing the same
US9119973B2 (en) 2008-12-30 2015-09-01 Takasago International Corporation Fragrance composition for core shell microcapsules
US8669287B2 (en) 2009-06-05 2014-03-11 Ajinomoto Co., Inc. Emulsifying preparation
JP2021061866A (en) * 2021-01-26 2021-04-22 ハウスウェルネスフーズ株式会社 Folic acid-containing acidic composition having excellent stability of folic acid

Also Published As

Publication number Publication date
JPH0527376B2 (en) 1993-04-21

Similar Documents

Publication Publication Date Title
DE60026611T2 (en) DRINKING OMEGA-3 PREPARATION
AU2006304046B2 (en) Microemulsions for use in food and beverage products
IE60088B1 (en) Microemulsions of oil in water and alcohol
JPH11514221A (en) New process
JP2741093B2 (en) Production method of emulsion composition for food and drink
JPS61260860A (en) Method of providing acidic drink with fragrance, color or turbidity
JP5192356B2 (en) Emulsified composition for beverage
JP4381665B2 (en) Tea drink containing oil-soluble components of tea
JPH07107927A (en) Emulsified composition
JP3516968B2 (en) Emulsion composition for acidic protein drinks
JP3342550B2 (en) Formulations containing water-soluble hemicellulose
EP0146618B1 (en) Beverage clouding agent based on carnauba wax
CN100456958C (en) Method of preventing flavor component from degradation
JPH09107911A (en) Production of powdery perfume
JP3057133B2 (en) Water soluble powder flavor
JPH07171377A (en) Manufacture of emulsified composition
JPH01284333A (en) Emulsified liquid composition
JP3693394B2 (en) Method for producing emulsified fragrance
JP4448632B2 (en) New powder material that dissolves transparently
JP3266842B2 (en) Emulsions for citrus beverages
JPH0779712A (en) Preparation containing water-soluble hemicellulose
JPS623748A (en) Emulsion composition
JP3504373B2 (en) Emulsion composition
JPH03127970A (en) Coloring of drink
JPS6374457A (en) Stable emulsion composition for food and drink

Legal Events

Date Code Title Description
LAPS Cancellation because of no payment of annual fees