JPS6258954A - Pulverization of edible oily material - Google Patents

Pulverization of edible oily material

Info

Publication number
JPS6258954A
JPS6258954A JP60197777A JP19777785A JPS6258954A JP S6258954 A JPS6258954 A JP S6258954A JP 60197777 A JP60197777 A JP 60197777A JP 19777785 A JP19777785 A JP 19777785A JP S6258954 A JPS6258954 A JP S6258954A
Authority
JP
Japan
Prior art keywords
oil
starch
carboxylic acid
acid ester
oily material
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
JP60197777A
Other languages
Japanese (ja)
Inventor
Kinya Sato
佐藤 金弥
Masaharu Yamori
矢守 正治
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 JP60197777A priority Critical patent/JPS6258954A/en
Publication of JPS6258954A publication Critical patent/JPS6258954A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain the pulverized edible oily material having high content of the titled material and excellent durability and storage stability, by using a film-forming agent consisting of a combination of gum arabic and a decom posed starch carboxylic acid ester having a specific viscosity. CONSTITUTION:A starch carboxylic acid ester having a viscosity of 20-1,000cps (as 30wt% aqueous solution at 25 deg.C) is used in combination with gum arabic as a film-forming agent. An edible oily material is pulverized usually by emulsify ing the edible oily material together with the film-forming agent and drying the emulsified liquid.

Description

【発明の詳細な説明】 槍1」二Δ泗JL吏万一 本発明は、可食性油性材料の粉末化方法に関し、更に詳
しくは、精油、動植油脂類、油溶性色素類、油溶性ビタ
ミン類などの可食性油性材料を被膜形成剤を用いて粉末
化する際に、(1)粘度約20〜約1.000cpS(
30重量%水溶液、25℃)を有するデンプンカルボン
酸エステル分解物と(2)アラビアガムを被膜形成剤と
することを特徴とする可食性油性材料の粉末化方法に関
する。この方法によれば、上記(1)及び(2)の組み
合わせを充足する被膜形成剤を用いて該油性材料を乳化
処理した後、得られた乳化液を乾燥して風味、色調−の
・保′持効果及び経時安定性に優れた、可食性油性材料
の粉末化物を提供できる。
[Detailed Description of the Invention] The present invention relates to a method for powderizing edible oil-based materials, more specifically, essential oils, animal and vegetable oils, oil-soluble pigments, and oil-soluble vitamins. When powdering edible oil-based materials such as
The present invention relates to a method for powdering an edible oily material, characterized in that a starch carboxylic acid ester decomposition product having a 30% by weight aqueous solution (25° C.) and (2) gum arabic are used as film forming agents. According to this method, after the oil-based material is emulsified using a film-forming agent that satisfies the combination of (1) and (2) above, the resulting emulsion is dried to preserve flavor, color tone, and It is possible to provide a powdered edible oil-based material that has excellent retention effects and stability over time.

(1へW乱 従来可食性油性材料を粉末化する方法としては、アラビ
アガムなどの植物性〃ム質、ゼラチンやカゼインなどの
ごときたん白質、或いはショ糖脂肪酸エステル、レシチ
ンなどの界面活性剤とデキストリン等を油脂と共に礼化
し、噴霧乾燥などによって粉末化する方法が広く行なわ
れている。
(Go to 1) Conventional methods for powdering edible oil-based materials include vegetable mucilages such as gum arabic, proteins such as gelatin and casein, or surfactants such as sucrose fatty acid esters and lecithin. A widely used method is to make dextrin and the like together with fats and oils and powder it by spray drying or the like.

また上記の如き一般的な方法では油性材料含有量に限界
があるため、例えば微結晶セルロースとり溶性たん白質
を用いた高油III含有粉末を製造する方法も提案され
ている(特公昭41−1415号、特公昭41−154
0号及び特公昭44−6202号公報)。
Furthermore, since there is a limit to the amount of oily material contained in the above-mentioned general methods, a method has also been proposed for producing a high-oil III-containing powder using, for example, microcrystalline cellulose and soluble protein (Japanese Patent Publication No. 41-1415 No., Special Publication Showa 41-154
No. 0 and Japanese Patent Publication No. 44-6202).

更に、澱粉と置換ノカルポン酸とのエステルを特定粘度
となる様に加水分解した澱粉誘導体を用いて、食用脂肪
を乳化した二マルシaンをスプレーなどにより乾燥する
蛋白質不含のコーヒークリーム及びその製造法も提案さ
れている(特開昭58−212743号公報)。
Furthermore, protein-free coffee cream is produced by drying Dimarcian, which is an emulsification of edible fat, by spraying or the like using a starch derivative obtained by hydrolyzing an ester of starch and a substituted nocarboxylic acid to a specific viscosity, and the production thereof. A method has also been proposed (Japanese Unexamined Patent Publication No. 58-212743).

明が  しようと る  ヴ しかしながら上記従来方法においては、例えばアラビア
ガム、カゼイン、ゼラチンなどの保護コロイド物質を用
いた場合にはその乳化力に限界があるため高含油粉末は
得られず、加えて比較的高価となる欠点があった。
However, in the conventional method described above, when a protective colloid substance such as gum arabic, casein, or gelatin is used, it is not possible to obtain a powder with high oil content due to its limited emulsifying power. The drawback was that it was expensive.

また、微結晶セルロースやヒエームド・シリカなどの油
性物質を吸着する能力の大きい有機もしくは無機物質微
粉体を添加した場合は、油性材料の含有量及び得られた
粉末の流動性(滑沢性)は改善されるが、かかる水不溶
性物質の添加により用途が制限される不都合があった。
In addition, when adding organic or inorganic fine powder that has a large ability to adsorb oily substances such as microcrystalline cellulose or fused silica, the content of the oily material and the fluidity (smoothness) of the obtained powder may be Although this is an improvement, the addition of such a water-insoluble substance has the disadvantage that its applications are limited.

特開昭58−212743号公報提案によるデンプンカ
ルボン酸エステル分解物は、乳化力が優れており、該分
解物単独で用いても比較的多量の油性物質を含有した粉
末が得られることが知られている。しかしながら該分解
は被膜形成能に関しては必ずしも満足できるものではな
く、例えば、該分解物を用いて粉末化した揮発性香気物
質、油溶性色素類及び脂溶性ビタミン類などの粉末にお
いて、保存安定性が不十分であった。
It is known that the starch carboxylic acid ester decomposition product proposed in JP-A-58-212743 has excellent emulsifying power, and that even if the decomposition product is used alone, a powder containing a relatively large amount of oily substances can be obtained. ing. However, this decomposition is not necessarily satisfactory in terms of film-forming ability, and for example, powders of volatile aroma substances, oil-soluble pigments, and fat-soluble vitamins that are made using the decomposed products have poor storage stability. It was insufficient.

本発明者等は上記デンプンカルボン酸エステル分解物の
優れた乳化力を生かし、且つ被膜形成能の改善方法につ
いて研究した。その結果、粘度が約20−約1 *00
0cps(30重皿%水溶液、25℃、以下同じ)を有
するデンプンカルボン酸エステル分解物にアラビアガム
を添加併用することによって、該デンプンエステル分解
物の乳化特性を変えることなく、その被膜形成能を顕著
に改善でさることを発見した。
The present inventors made use of the excellent emulsifying power of the starch carboxylic acid ester decomposition product and conducted research on a method for improving the film-forming ability. As a result, the viscosity is about 20 - about 1 *00
By adding gum arabic to a starch carboxylic acid ester decomposition product having 0 cps (30% aqueous solution, 25°C, the same applies hereinafter), the film-forming ability of the starch ester decomposition product can be improved without changing the emulsification properties of the starch ester decomposition product. I found that there was a noticeable improvement.

従って本発明の目的は、(1)粘度約20〜約1゜00
0 cpsを有するデンプンカルボン酸エステル分解物
とく2)アラビアガムを被膜形成剤として可食性油性材
料を乳化し、その乳化物を噴n乾燥法などによって粉末
化することによって、上記(1)又は(2)の夫々単独
ではとうてい達成できない効果、即ち油性材料の含量が
高く、潮解性や吸湿性の少ない改!!された被膜により
、粉体内に包含される油性材料の持続性保存安定性が飛
躍的に改善された可食性油性材料の粉末化物を提供する
にある。
Therefore, the object of the present invention is to (1) reduce the viscosity from about 20 to about 1°00;
2) By emulsifying an edible oily material using gum arabic as a film forming agent and powdering the emulsion by a spray drying method, the above (1) or ( Effects that cannot be achieved by each of 2) alone, namely, a high content of oily materials and low deliquescent and hygroscopic properties! ! The object of the present invention is to provide a powdered product of an edible oil-based material in which the sustained storage stability of the oil-based material contained in the powder is dramatically improved due to the coated coating.

本発明の上記目的及び更に多くの他の目的及び利点は以
下の説明から一層明らかになるであろう。
The above objects and many other objects and advantages of the present invention will become more apparent from the following description.

11  σを iするための 本発明における可食性油性材料としては、例えばオレン
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
レオレンジ類;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*)J、t19o
ay4tb″ey>″8″″004”1油・ゞ′2′9
・YP t ′A油・ゞ′2′8・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、ナタネ油、コーン油、オリ      
  1−プ油、ヤシ油、サフラワー油、ヒマワリ油、米
油、牛脂、豚脂、魚油などの動植物油脂類;ロノン、コ
ーパル、ダンマル、エレミ、エステルがなどの植物性樹
脂類;C1〜CI2の中鎖飽和脂肪酸トリグリセライド
、シュークロース・ジアセテート・ヘキサイソプチレー
)(SAIB)などの比重調整剤及びこれらの油性材料
の任意の混合物を例示することができる。
The edible oily materials in the present invention for increasing 11σ include, for example, citrus essential oils such as orange, lemon, lime, and grapefruit; plant essential oils such as flower essential oils; peppermint oil, spearmint oil, and spice oil; cola nut extract; , oily extracts such as coffee extract, wanilla extract, cocoa extract, black tea extract, spice extract, and their oleoranges; synthetic fragrance compounds, oil-based blended fragrance compositions, and any mixtures thereof. oil-based flavoring agents such as; and β-
Carotene, paprika pigment, annatto color *) J, t19o
ay4tb″ey>″8″″004″1 oil・ゞ′2′9
・YP t'A oil・ゞ′2′8・butry:
Fat-soluble vitamins such as acid esters, natural vitamin E mixtures; soybean oil, rapeseed oil, corn oil,
1- Animal and vegetable oils such as oil, coconut oil, safflower oil, sunflower oil, rice oil, beef tallow, pork fat, and fish oil; vegetable resins such as ronone, copal, dammar, elemi, and ester; C1 to CI2 Examples include medium-chain saturated fatty acid triglycerides, specific gravity adjusters such as sucrose diacetate hexisoptyle (SAIB), and arbitrary mixtures of these oil-based materials.

また本発明でいう(1)に属するデンプンカルボン酸エ
ステル分解物とは、デンプンカルボン酸エステルの分解
物及びデンプン分解物のカルボン酸エステルの何れをも
意味する。かかるデンプンカルボン酸エステル分解物の
例としては、例えば米国特許No、2 =661 +3
49号、同No、3.’455.838号等に開示され
ている如く、デンプンをアルカリ性媒質中で置換ノカル
ボン酸環状無水物、例えば置換無水コハク酸、置換無水
グルグル酸、置換無水アノビン酸等と反応させることに
よって得られるデンプンカルボン酸エステルを公知の分
解方法例えば、熱、酸もしくは酵素処理によって分解し
、その30重世%水溶液の粘度が25℃において約20
〜約1,000cpsとなるまで分解して得られる分解
物を例示することができる。
In addition, the starch carboxylic acid ester decomposition product belonging to (1) in the present invention means both a starch carboxylic acid ester decomposition product and a starch decomposition product carboxylic acid ester. Examples of such starch carboxylic acid ester decomposition products include, for example, US Patent No. 2 = 661 + 3
No. 49, same No. 3. '455.838, etc., starch obtained by reacting starch with a substituted nocarboxylic acid cyclic anhydride, such as substituted succinic anhydride, substituted gluguric anhydride, substituted anobic anhydride, etc., in an alkaline medium. The carboxylic acid ester is decomposed by a known decomposition method such as heat, acid or enzyme treatment, and the viscosity of a 30% aqueous solution at 25°C is about 20%.
An example of this is a decomposition product obtained by decomposing it to about 1,000 cps.

かかるデンプンカルボン酸エステル分解物は上記の如く
して調製することができるが、市場でも人手でき、同様
に利用することができる。市販品の例としては、例えば
米国ナシヨナル スターチアンド ケミカル コーポレ
ーション(NationalS tarcb and 
Chemical ’Corporation(Bri
dgwat−er、 NcすJ ersey) )から
発売されている商品名CAPSUL、ビユリティー〃ム
(PURITYGUM)1773、及びビユリティ−〃
ム(PUR1’l’Y  GUM)BEなどを利用する
ことができる。
Such a starch carboxylic acid ester decomposition product can be prepared as described above, but it can also be prepared manually and used in the same manner in the market. Examples of commercially available products include, for example, National Starch and Chemical Corporation (National Starch and Chemical Corporation).
Chemical 'Corporation (Bri
Product names CAPSUL, PURITYGUM 1773, and PURITYGUM 1773, which are sold by dgwat-er,
It is possible to use, for example, GUM(PUR1'l'Y GUM)BE.

曲記した粘度範囲を外れた場合は、例えば30%水溶液
の粘度(25℃)が20cps以下の場合は、乳化性が
劣るためアラビアガムの増量が不可決となり経済性に問
題が生じ、また粘度が1.000cpsを超えた場合は
、例えば噴霧乾燥などの場合は多量の水を必要とし、同
様に乾燥コストが高くなる問題がある。なお、本発明に
おいて粘度は下の如き条件で測定決定する。
If the viscosity falls outside the specified viscosity range, for example, if the viscosity of a 30% aqueous solution (at 25°C) is less than 20 cps, the emulsifying property will be poor, making it impossible to increase the amount of gum arabic, causing problems in economic efficiency, and If it exceeds 1.000 cps, for example, spray drying requires a large amount of water, which similarly raises the problem of high drying costs. In the present invention, the viscosity is measured and determined under the following conditions.

粘度測定法:デンプンカルボン酸エステル分解物の30
重皿%水患濁液を約90〜95℃にて15分間加熱洛詳
解後冷却し、蒸発水分を補正した後、B型粘度計(東京
計器製作所gi)を用いて、ローターNo、3、回転数
60 rpm、温度25℃±0゜5℃における粘度を測
定決定した。
Viscosity measurement method: Starch carboxylic acid ester decomposition product 30
After heating the suspension of % water in a heavy plate for 15 minutes at approximately 90 to 95°C, cooling and correcting the evaporated water, using a B-type viscometer (Tokyo Keiki Seisakusho GI), rotor No. 3, rotating. The viscosity was determined at several 60 rpm and a temperature of 25°C±0°5°C.

また、前記(2)のアラビアガムとしては例えば第10
改正日本薬局方に記載されている如き規格のものを例示
できる。
In addition, as gum arabic in the above (2), for example, the 10th gum arabic
Examples include those of the standards described in the revised Japanese Pharmacopoeia.

本発明においては上記(1)デンプンカルボン酸エステ
ル分解物と共に被膜強化剤として(2)アラビアガムを
併用する。かがる(1)と(2)の混合割合は、適宜に
選択し得るが、好ましい範囲を例示すれば、例えば(1
)の1重量部(以下ことわりのない限りすべて重量で表
わす)に対して(2)を約0.01〜約2部、殊に好ま
しくは約80°〜約0.5部の如き割合を例示すること
ができる。
In the present invention, (1) starch carboxylic acid ester decomposition product and (2) gum arabic are used together as a film strengthening agent. The mixing ratio of Kagaru (1) and (2) can be selected as appropriate, but examples of preferred ranges include (1)
(2) is exemplified in a ratio of about 0.01 to about 2 parts, particularly preferably about 80° to about 0.5 parts, to 1 part by weight of (2) (hereinafter all expressed by weight unless otherwise specified). can do.

本発明において、可食性油性材料二上記(1)のデンプ
ンカルボン酸エステル分解物と(2)アラビアガムから
なる被膜形成剤の割合としては、例えば1:約0.1〜
約500.好ましくは1:約0.2〜約200の如き割
合を例示することができる。
In the present invention, the ratio of the film forming agent consisting of the starch carboxylic acid ester decomposition product of (1) above and (2) gum arabic to the edible oily material is, for example, 1: about 0.1 to
Approximately 500. Preferably, the ratio is 1:about 0.2 to about 200.

更に本発明においては所望により、上記(1)及V(2
)加えて他の保護コロイド物質を添加配合するさことが
でき、かかる保護コロイド物質としては、例えば、接種
もしくはロキシー澱粉から誘導される酵素変性デンプン
、酸化デンプン、酸処理デンプン、及びデキストリンな
どの分解デンプン類:カルボキシメチルデンプン、ヒド
ロキシアルキルデンプン、エピクロルヒドリンデンプン
、アリルテ゛ンプンなどのデンプンエーテルンモノリン
酸エステルナトリウム、架橋型ノスターチホス7エート
、アルキルシスターチホス7二一トなどのデンプンリン
酸エステル類及びこれらデンプン講導体の加水分解物;
又はプルラン、ペクチン、ローカストビン〃ム、ゼラチ
ン、7ルイン酸及びその塩類、カラーギナン、カラヤガ
ム、キサンタンガム、グアー〃ム、スクレロ〃ム、トラ
ガントガム、タマリンド種子多糖類、7アーセレランな
どの天然起源の安定剤からなる群から選ばれた1種もし
くは281以上の混合物を例示することがでさる。
Furthermore, in the present invention, the above (1) and V(2) may be added as desired.
) In addition, other protective colloid substances can be added and formulated, such as enzyme-modified starches derived from inoculation or roxy starch, oxidized starches, acid-treated starches, and decomposed starches such as dextrins. Starches: Starch phosphate esters such as carboxymethyl starch, hydroxyalkyl starch, epichlorohydrin starch, allyl starch, starch ether monophosphate sodium, crosslinked nostarch phosphate 7-ate, alkyl sister starch phosphate 7-2-1, and these starches. Hydrolyzate of conductor;
or from stabilizers of natural origin such as pullulan, pectin, locustvin, gelatin, 7-ruic acid and its salts, carrageenan, karaya gum, xanthan gum, guar, sclerom, gum tragacanth, tamarind seed polysaccharide, 7-arselan, etc. Examples include one type or a mixture of 281 or more selected from the group consisting of:

これらの保護コイド物質の添加量としては、前記(1)
と(2)の合計量に対して例えば約50%以下の如き添
加量を例示することができる。
The amount of these protective coid substances added is as specified in (1) above.
For example, the amount added may be about 50% or less of the total amount of (2) and (2).

次に本発明の好ましい一実施態様を例示すれば、例えば
先ず水1部に対して(1)及び(2)からなる被膜形成
剤約0.1〜約1部を加えて混合分散後、約80°〜約
100℃にて約5〜約20分加熱溶解と共に殺菌を行う
。約40℃以下に冷却し、得られた溶液に可食性油性材
料の所要量を添加し、例えば1’ K−ホモミキサー(
特殊磯化工業製)等を用いて約5,000−約10e0
00rpa+の回転数で、約5〜約20分闇乳化処理す
る。所望により、更に高圧ホモジナイザーもしくはコロ
イドミルなどを用いて乳化処理しても良い。
Next, to illustrate a preferred embodiment of the present invention, for example, first, about 0.1 to about 1 part of the film forming agent consisting of (1) and (2) is added to 1 part of water, mixed and dispersed, and then about Dissolution and sterilization are performed by heating at 80° to about 100°C for about 5 to about 20 minutes. Cool to below about 40°C and add the required amount of edible oily material to the resulting solution, for example in a 1' K-Homo mixer (
Approximately 5,000 - approximately 10e0 using special Isoka Kogyo) etc.
Emulsify in the dark for about 5 to 20 minutes at a rotation speed of 00 rpm. If desired, emulsification treatment may be further carried out using a high-pressure homogenizer or a colloid mill.

上記乳化処理の際に所望により、水溶性色素類、動植物
の水抽出エキス、アミノ酸、核酸類、有機酸塩類などの
呈味剤を添加配合することもできる。
During the emulsification process, flavoring agents such as water-soluble pigments, water-extracted animal and plant extracts, amino acids, nucleic acids, and organic acid salts may be added, if desired.

乳化処理によって得られたエマルシaンは公知の常用の
乾燥手段例えば、噴霧乾燥、真空乾燥、ドラム乾燥、泡
沫乾燥、凍結乾燥、好ましくは噴霧乾燥によって粉末化
することができる。
The emulsion obtained by the emulsification process can be pulverized by known conventional drying means such as spray drying, vacuum drying, drum drying, foam drying, freeze drying, preferably spray drying.

艷−1 本発明方法は、(1)デンプンカルボン酸エステル分解
物と(2)7ラビ71JPムを組み合せたことにより、
従来油性材料の被膜材として不充分であったデンプンカ
ルボン酸エステル分解物の被a能を顕著に改善し、上記
両者の相剰作用による高含油、高安定性を有する油性材
料の粉末化が達成された。
艷-1 The method of the present invention combines (1) a starch carboxylic acid ester decomposition product and (2) 7Rabi 71JP Mu,
The a-covering ability of starch carboxylic acid ester decomposition products, which were conventionally insufficient as coating materials for oil-based materials, has been significantly improved, and due to the mutual action of the above, it has been possible to powderize oil-based materials with high oil content and high stability. It was done.

以下実施例により本発明の敗態様を更に詳しく説明する
Hereinafter, the failure aspects of the present invention will be explained in more detail with reference to Examples.

に−1L」1 実施例 1 30重量%水溶液の粘度(25℃)が約50epsであ
ろデンプンカルボン酸エステル分解物(カプルス:ナシ
鱈ナルスターチ社製)700g及び7ラビ7、fム20
0gの混合物を水1500gに加えて溶解後、95℃に
て15分間殺菌を行った。約40″Cまで冷却後、ペパ
ーミント油100gを加え均一に分散し、次いで高圧ホ
モジナイザーを用いて100 kg/cm”にて乳化し
た。得られた乳化液をエロ・アトマイザ−にて、熱風温
度180℃で噴霧乾燥し、乾燥粉末950ビを得た(本
発明品No、1)。
Example 1 The viscosity (25° C.) of a 30% aqueous solution is about 50 eps. 700 g of a starch carboxylic acid ester decomposition product (Kapulus: manufactured by Nashidara Narstarch Co., Ltd.) and 7 Rabi 7, fm 20
After dissolving 0 g of the mixture in 1500 g of water, sterilization was performed at 95° C. for 15 minutes. After cooling to about 40''C, 100g of peppermint oil was added and uniformly dispersed, and then emulsified at 100 kg/cm'' using a high-pressure homogenizer. The obtained emulsion was spray-dried using an erotic atomizer at a hot air temperature of 180°C to obtain a dry powder of 950 mm (invention product No. 1).

比較例 1 実施例1において、アラビアガム200gをデンプンカ
ルボン酸エステル分解物(カブスル、同上)200.で
置き換え、デンプンカルボン酸エステル分解物を単独で
900gとしたほかは、全て実施例1と同一条件によっ
て行ない、乾燥粉末930、を得た(比較品No、1)
Comparative Example 1 In Example 1, 200 g of gum arabic was mixed with 200 g of starch carboxylic acid ester decomposition product (Cabusul, same as above). The procedure was carried out under the same conditions as in Example 1, except that 900 g of starch carboxylic acid ester decomposition product was used alone, and dry powder 930 was obtained (comparative product No. 1).
.

参考例 1 実施例1(本発明品No、1)及び比較例1(比較品N
o、1)で得られたペパーミント油の乾燥粉末を、チュ
ーイン〃ム基材にそれぞれ2.0重皿%添加し、常法に
よる板ガムを調整した。このチューインガムを良く訓練
された15名の検査員を用いて、官能評価を行った。そ
の結果を第1表に示した。
Reference Example 1 Example 1 (Invention Product No. 1) and Comparative Example 1 (Comparative Product No.
2.0% of the dry powder of peppermint oil obtained in step 1) was added to the chewing gum base material, and chewing gum was prepared by a conventional method. A sensory evaluation of this chewing gum was conducted using 15 well-trained examiners. The results are shown in Table 1.

第1表 第1表の結果から明らかな如く、本発明品は被膜強化さ
れ、香味の持続性におそい者しく優れていた。
As is clear from the results shown in Table 1, the product of the present invention had a strengthened coating and was excellent in flavor persistence.

実施例 2 30重量%水溶液の粘度(25℃)が約420cpSを
有するデンプンカルボン酸エステル分解物(ピユリティ
−〃ム1773、商品名ナシaナルスターチ製)300
g、7うとア〃ムsog及1デキスト’7ン(DElo
)600gを水1200gL:加えて溶解し、加熱殺菌
して冷却後、レモン油50gを加えて実施例1と同様に
乳化処理後噴霧乾燥して、レモン油粉末960gを得た
(本発明品No、2)。
Example 2 Starch carboxylic acid ester decomposition product having a 30% by weight aqueous solution having a viscosity (25°C) of approximately 420 cpS (Purity 1773, trade name manufactured by Nasional Starch) 300
g, 7 and am sog and 1 dext'7 (DElo
) 600g was added to 1200gL of water, dissolved, heat sterilized, cooled, 50g of lemon oil was added, emulsified in the same manner as in Example 1, and spray-dried to obtain 960g of lemon oil powder (inventive product No. , 2).

比較例 2 実施例2においてアラビアガム50gに代えてピユリテ
ィ−〃ム1773を50g増量して350gとしたほか
は、全て実施例1と同じ条件によってレモン油粉末95
5gを得た(比較品No、2)。
Comparative Example 2 Lemon oil powder 95 g was prepared under the same conditions as in Example 1 except that 50 g of Gum Arabic was replaced with 50 g of Piuritim 1773 to 350 g.
5 g was obtained (comparative product No. 2).

参考例 2 実施例2(本発明品No、2)及ゾ比較例2(比較品N
o、2)で得られたレモン油粉末を、それぞれ下記の割
合で配合して、粉末飲料を調製し、ポリエチレン−アル
ミ箔−ポリエチレンのラミネート袋に各20g宛小分け
しで充填しヒートシールした。
Reference Example 2 Example 2 (Invention Product No. 2) and Comparative Example 2 (Comparative Product No.
A powdered beverage was prepared by blending the lemon oil powders obtained in steps (o) and 2) in the following proportions, and the mixture was filled into polyethylene-aluminum foil-polyethylene laminate bags in portions of 20 g each and heat-sealed.

この小袋詰粉末飲料を37℃、Rl−180%の条件と
、4℃の冷蔵庫にそれぞれ2週間保存後各1袋<20g
)を150nfの水に溶解し、冷蔵庫保存品を標準とし
て、実施例1と同様の方法で官能評価を行った。その結
果を第2表に示す。
After storing this sacheted powdered beverage at 37℃, Rl-180% and in a refrigerator at 4℃ for 2 weeks, each bag <20g.
) was dissolved in 150 nf water, and sensory evaluation was performed in the same manner as in Example 1 using the refrigerator-stored product as a standard. The results are shown in Table 2.

粉末飲料配合処方 グラニユー糖        100g無水クエンI’
ll             2,5gリンゴ酸  
           0.7gクエン酸ナトリウム 
       0.2gレモン油粉末        
  1.5g第  2  表 第2表の結果から明らかな如く、本発明品は、レモン油
の劣化程度が僅少で、保存性が者しく改@されていた。
Powdered Beverage Formula Granulated Sugar 100g Anhydrous Citric I'
ll 2.5g malic acid
0.7g sodium citrate
0.2g lemon oil powder
1.5g Table 2 As is clear from the results in Table 2, the product of the present invention had a slight degree of deterioration in lemon oil, and its preservability was clearly improved.

実施例 3 実施例2で使用したと同じビユリティ−〃ム1773を
250g及びアラビアガム50gを水1200gに加え
て溶解し、殺菌冷却後、ゴマ油700gを加元てTK−
ホモミキサー(特殊機化工業)を用いて8,000rp
mにて10分間乳化した。次いでこの乳化液を実施例1
と同様の条件にで噴n乾燥し、ゴマ油粉末940gを得
た(本発明No、2)。
Example 3 250g of the same Biulitim 1773 used in Example 2 and 50g of gum arabic were dissolved in 1200g of water, and after sterilization and cooling, 700g of sesame oil was added to make TK-
8,000 rpm using a homomixer (Tokushu Kika Kogyo)
The mixture was emulsified at m for 10 minutes. Next, this emulsion was prepared in Example 1.
It was spray-dried under the same conditions as above to obtain 940 g of sesame oil powder (Invention No. 2).

この粉末は極めて流動性が良く、また乾燥機内で部の壁
面への付着もみられず、又保存安定性も優れていた。
This powder had extremely good fluidity, did not adhere to the walls in the dryer, and had excellent storage stability.

実施例 4 30重量%水溶液の粘度(25℃)が約700cpSで
あるデンプンカルボン酸エステル分解物(ビユリティ−
〃ムBE、ナショナルスターチ社製)100g1アラビ
ア〃ム50g及びデキストリン(DE8)750.を水
1000g%こ溶解し、90℃、15分間殺菌後冷却し
た。得られた水溶液にバニラオレオレノン(艮谷用香料
1)i o ogを添加し、均一に混合後、TK−ホモ
ミキサーを用いて乳化処理後、噴霧乾燥し、バニラ7レ
ーバー粉末960gを得たく本発明品No、3)。
Example 4 A starch carboxylic acid ester decomposition product (biility-
100 g of Lamb BE (manufactured by National Starch) 50 g of Arabic Lamb and 750 g of dextrin (DE8). was dissolved in 1000g% of water, sterilized at 90°C for 15 minutes, and then cooled. Add vanilla oleolenon (Fragrance 1 for Asutani) io og to the obtained aqueous solution, mix uniformly, emulsify using a TK-Homo mixer, and spray dry to obtain 960 g of Vanilla 7 Raver powder. Invention product No. 3).

実施例 5 実施例1で用いたビユリティ−〃ム1773を300g
、アラビアガム100g、ゼラチン10g及びパインデ
ックスNo、100(デキストリン、松谷化学)550
.を水1700E+に溶解し、殺菌、冷却後、ワサビフ
レーバー(艮谷111香料製品)1508及びグリーン
カラーTH(クチナシ色素、艮谷用香料製品)10gを
加えてT K−ホモミキサーに一1+川lし傾 Ij/
欣秘6ルロ耗消息社−−n古ケ抛1ワサビフレーバーパ
ウダー1kgを得た(本発明品No、5)。このワサビ
フレーバーは室温で6+月保存後も製造時と同等の強い
辛味性を保持していた。
Example 5 300g of Bulitym 1773 used in Example 1
, 100 g of gum arabic, 10 g of gelatin and Pine Index No. 100 (dextrin, Matsutani Chemical) 550
.. Dissolved in water 1700E+, sterilized and cooled, added 1508 wasabi flavor (Hasutani 111 flavor products) and 10 g of green color TH (gardenia pigment, fragrance products for Hasutani), and mixed it in a TK-Homo mixer. Tilt Ij/
1 kg of wasabi flavor powder was obtained (product No. 5 of the present invention). This wasabi flavor retained the same strong spiciness as at the time of manufacture even after storage for 6+ months at room temperature.

実施例 6 実施例4で用いたビユリティ−〃ムBE500g、アラ
ビアガム20g及びデキストリン(D E 8 )30
0gを水1700gに溶解し、殺菌冷却後、パプリカ色
素(カラーバリユー10万)200gを添加し、均一に
分散後、実施例1と同様に乳化処理後噴霧乾燥し、パプ
リカ色素粉末935gを得た(本発明品No、6)。得
られた粉末パプリカ色素は3ケ月保存後も退色がなく、
安定であった。
Example 6 500 g of the building blocks used in Example 4, 20 g of gum arabic, and 30 g of dextrin (D E 8 )
0g was dissolved in 1700g of water, and after sterilization and cooling, 200g of paprika pigment (Color Value 100,000) was added and dispersed uniformly. After emulsification treatment in the same manner as in Example 1, spray drying was performed to obtain 935g of paprika pigment powder. (Product No. 6 of the present invention). The obtained powdered paprika pigment did not fade even after being stored for 3 months.
It was stable.

魚濃じL沈迷一 本発明方法によれば、従来、油性材料を粉末化する際の
被膜材として利用する場合に、乾燥時の繰作性、被Nf
f1力が劣る等の理由で、不適当とされた、例えば30
%水溶液の粘度(25℃)が30epSの如き低粘度の
デンプンカルボン酸エステル分解物をも利用可能となっ
た。かかる低粘度の該分解物を利用することによる、乾
燥前の油性材料111シ 乳化後に占める水分含量を着しく減少することができ、
工業的に極めて有利である。
According to the method of the present invention, when conventionally used as a coating material when powdering oil-based materials, repeatability during drying, Nf
For example, 30
It has also become possible to use starch carboxylic acid ester decomposition products with low viscosity, such as a viscosity of 30 epS in an aqueous solution (25° C.). By using such a low-viscosity decomposition product, the water content of the oil-based material 111 before drying and after emulsification can be significantly reduced,
It is extremely advantageous industrially.

しかも従来、被覆性に問題のあったデンプンカルボン酸
エステル分解物の欠点をカバーし、例えば含油量約70
〜約90%にも及ぶ油性材料の粉末を得ることを可能に
した。更に得られた粉末は被膜の強度が大きく、殊に揮
散もしくは変質し易い香気成分の保存安定性を顕著に改
善し、加えて賦香した際の香気持続性も着しく改善され
た。
In addition, it covers the drawbacks of starch carboxylic acid ester decomposition products that conventionally had problems with coating properties, and has an oil content of about 70%.
It was possible to obtain powder of oil-based materials up to about 90%. Furthermore, the obtained powder had a high coating strength, and the storage stability of the aroma components, which are easily volatilized or deteriorated, was significantly improved, and in addition, the persistence of the aroma when perfumed was significantly improved.

本発明によって得られた可食性油性材料の粉末は、キャ
ンディ−、チューインガム、錠菓、和洋生菓子などの菓
子類、果汁飲料、豆乳飲料、乳飲料、コーラ飲料などの
飲料類、ハム、カマボコなどの水醒産加工品、バター、
チーズなどの乳製品、調味量、栄養ドリンク、歯磨、日
中剤、医薬品など、多方面の用途に効果的に利用するこ
とができる。
The powder of the edible oily material obtained by the present invention can be used for confectionery such as candy, chewing gum, tablet confectionery, Japanese and Western fresh sweets, beverages such as fruit juice drinks, soy milk drinks, milk drinks and cola drinks, ham and kamaboko. Processed products from Suisei, butter,
It can be effectively used in a wide range of applications, including dairy products such as cheese, seasonings, energy drinks, toothpaste, daytime remedies, and pharmaceuticals.

Claims (1)

【特許請求の範囲】 1、可食性油性材料を被膜形成剤を用いて粉末化する際
に、 (1)粘度約20〜1,000cps(30重量%水溶
液、25℃)を有するデンプンカルボン酸エステル分解
物及び (2)アラビアガム を被膜形成剤とすることを特徴とする可食性油性材料の
粉末化方法。
[Claims] 1. When an edible oily material is powdered using a film forming agent, (1) a starch carboxylic acid ester having a viscosity of about 20 to 1,000 cps (30% aqueous solution, 25°C); A method for powdering an edible oily material, comprising using a decomposition product and (2) gum arabic as a film forming agent.
JP60197777A 1985-09-09 1985-09-09 Pulverization of edible oily material Pending JPS6258954A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60197777A JPS6258954A (en) 1985-09-09 1985-09-09 Pulverization of edible oily material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60197777A JPS6258954A (en) 1985-09-09 1985-09-09 Pulverization of edible oily material

Publications (1)

Publication Number Publication Date
JPS6258954A true JPS6258954A (en) 1987-03-14

Family

ID=16380173

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60197777A Pending JPS6258954A (en) 1985-09-09 1985-09-09 Pulverization of edible oily material

Country Status (1)

Country Link
JP (1) JPS6258954A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001128638A (en) * 1999-11-08 2001-05-15 Takasago Internatl Corp Powdered flavor preparation controlled in manifesting flavor
JP2001271089A (en) * 2000-03-24 2001-10-02 Snow Brand Milk Prod Co Ltd Spice formulated with amino acid
JP2002188095A (en) * 2000-12-21 2002-07-05 Fancl Corp Vegetable oil and fat powder and food composition containing the powder
JP2003073691A (en) * 2001-08-30 2003-03-12 Nof Corp Protein-free powdered fat composition and its use
JP2013051964A (en) * 2005-02-03 2013-03-21 Firmenich Sa Spray-dried compositions and their uses
US9376648B2 (en) 2008-04-07 2016-06-28 The Procter & Gamble Company Foam manipulation compositions containing fine particles
JP2018522537A (en) * 2015-05-27 2018-08-16 ジボダン エス エー Spray dry

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001128638A (en) * 1999-11-08 2001-05-15 Takasago Internatl Corp Powdered flavor preparation controlled in manifesting flavor
JP2001271089A (en) * 2000-03-24 2001-10-02 Snow Brand Milk Prod Co Ltd Spice formulated with amino acid
JP2002188095A (en) * 2000-12-21 2002-07-05 Fancl Corp Vegetable oil and fat powder and food composition containing the powder
JP2003073691A (en) * 2001-08-30 2003-03-12 Nof Corp Protein-free powdered fat composition and its use
JP2013051964A (en) * 2005-02-03 2013-03-21 Firmenich Sa Spray-dried compositions and their uses
US9376648B2 (en) 2008-04-07 2016-06-28 The Procter & Gamble Company Foam manipulation compositions containing fine particles
JP2018522537A (en) * 2015-05-27 2018-08-16 ジボダン エス エー Spray dry

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