JP2731397B2 - Method for producing instant thickened gelled product - Google Patents

Method for producing instant thickened gelled product

Info

Publication number
JP2731397B2
JP2731397B2 JP63167528A JP16752888A JP2731397B2 JP 2731397 B2 JP2731397 B2 JP 2731397B2 JP 63167528 A JP63167528 A JP 63167528A JP 16752888 A JP16752888 A JP 16752888A JP 2731397 B2 JP2731397 B2 JP 2731397B2
Authority
JP
Japan
Prior art keywords
gellan gum
acid
water
parts
gelled product
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.)
Expired - Lifetime
Application number
JP63167528A
Other languages
Japanese (ja)
Other versions
JPH0218487A (en
Inventor
二郎 藤尾
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.)
SANEIGEN EFU EFU AI KK
Original Assignee
SANEIGEN EFU EFU AI KK
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 SANEIGEN EFU EFU AI KK filed Critical SANEIGEN EFU EFU AI KK
Priority to JP63167528A priority Critical patent/JP2731397B2/en
Publication of JPH0218487A publication Critical patent/JPH0218487A/en
Application granted granted Critical
Publication of JP2731397B2 publication Critical patent/JP2731397B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、即席で増粘、ゲル化する物の製造法に係る
ものである。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a method for producing an instantly thickened and gelled material.

〔従来の技術〕 ジェランガムを用いて増粘、ゲル化状物をつくるため
にジェランガムの水溶液をつくるには90℃以上の加熱が
必要であった。
[Prior Art] Heating at 90 ° C. or higher was necessary to prepare an aqueous solution of gellan gum in order to form a gelled substance by using gellan gum to increase the viscosity.

そのため、高温に加熱し、かつその温度を保持するた
めの設備が必要であり、又、増粘、ゲル化させるために
は冷却設備が必要であった。
Therefore, equipment for heating to a high temperature and maintaining the temperature is required, and cooling equipment is required for thickening and gelling.

〔課題を解決するための手段〕[Means for solving the problem]

本発明はジェランガムの溶解速度を速める為にジェラ
ンガムを物理的に微粉砕することによりジェランガムを
150μm以下の微粒子にする。好ましくは75μm以下の
粒子径が望ましい。
The present invention provides gellan gum by physically pulverizing gellan gum to increase the dissolution rate of gellan gum.
Fine particles of 150 μm or less. Preferably, the particle diameter is 75 μm or less.

微粒子のジェランガムに金属イオン封鎖剤を混合し、
常水に加え30〜60秒攪拌することにより直ちにこの水溶
液は、増粘、ゲル化する。
Mix the sequestering agent with the fine gellan gum,
This aqueous solution is immediately thickened and gelled by stirring for 30 to 60 seconds in addition to ordinary water.

金属イオン封鎖剤としては、重合リン酸塩類、例え
ば、メタリン酸、ポリリン酸、ピロリン酸等の酸性、中
性、塩基性のナトリウム塩がある。
Examples of sequestering agents include polymerized phosphates, for example, acidic, neutral, and basic sodium salts such as metaphosphoric acid, polyphosphoric acid, and pyrophosphoric acid.

又、クエン酸、酒石酸、フマール酸、エチレンジアミ
ンテトラ酢酸、その他の有機酸等の酸性、中性、塩基性
のナトリウム塩がある。又フィチン酸、タンニン酸、ゲ
ンチジン酸等の有機化合物、その他があげられる。これ
らの金属イオン封鎖剤の添加量は微粒子ジェランガム10
0部に対して1〜200部であるが、この範囲に限定されな
い。
There are also acidic, neutral and basic sodium salts such as citric acid, tartaric acid, fumaric acid, ethylenediaminetetraacetic acid and other organic acids. Organic compounds such as phytic acid, tannic acid and gentisic acid, and others are also included. The amount of addition of these sequestering agents is 10
The amount is 1 to 200 parts with respect to 0 parts, but is not limited to this range.

微粒子にする方法としては、ボールミル粉砕、ハンマ
ーミル粉砕、奈良式粉砕、フェザーミル粉砕等、いずれ
の方法を用いてもジェランガムの粒子径を150μm以下
にすればよく、任意である。
As a method for forming fine particles, any method such as ball mill pulverization, hammer mill pulverization, Nara pulverization, and feather mill pulverization may be used as long as the particle diameter of gellan gum is 150 μm or less, and is arbitrary.

このようにして得られた微粒子のジェランガムと金属
イオン封鎖剤の混合物は冷水に可溶である。例えば、20
℃の水道水を使用した場合、30〜60秒攪拌することによ
って溶解し、粘ちょうな水溶液が得られる。
The mixture of the finely divided gellan gum and the sequestering agent thus obtained is soluble in cold water. For example, 20
When tap water at ℃ is used, it is dissolved by stirring for 30 to 60 seconds to obtain a viscous aqueous solution.

微粒子のジェランガムと金属イオン封鎖剤に酸性、中
性、塩基性の金属塩類、例えばCa、Mg等のアルカリ土類
金属塩、K、Na等のアルカリ金属塩、アンモニウム塩
類、アルミニウム塩類等を併用してもよい。
Acidic, neutral and basic metal salts such as alkaline earth metal salts such as Ca and Mg, alkali metal salts such as K and Na, ammonium salts, aluminum salts and the like are used in combination with the fine particle gellan gum and the sequestering agent. You may.

これらの塩類は、微粒子のジェランガムと金属イオン
封鎖剤よりも水に対する溶解速度の遅いものが望まし
い。例えばアルカリ土類金属塩の硫酸カルシウム(マグ
ネシウム)、リン酸1、2、3カルシウム(マグネシウ
ム)、クエン酸モノ、ジ、トリカルシウム(マグネシウ
ム)、グルコン酸カルシウム、炭酸又は重炭酸カルシウ
ム(マグネシウム)等の酸性塩、中性塩、又は、塩基性
塩、又はアルカリ金属塩としては、クエン酸モノ、ジ、
ナトリウム(カリウム)、酒石酸、フマール酸、アジピ
ン酸のモノ又はジカリウム(ナトリウム)、酸性メタリ
ン酸カリウム(ナトリウム)、ピロリン酸ナトリウム
(カリウム)、リン酸1カリウム等の無機酸や有機酸の
酸性塩、中性塩、塩基性塩、アンモニウム又はアルミニ
ウム塩としては、リン酸1アンモニウム、脱水乾燥した
アンモニウムミョウバン、ミョウバン類又はグルコノデ
ルタラクトンのように水の中で徐々に加水分解し、酸性
物質となるものを併用してもよい。
It is desirable that these salts have a lower dissolution rate in water than gellan gum of fine particles and a sequestering agent. For example, alkaline earth metal salts calcium sulfate (magnesium), phosphoric acid 1,2,3 calcium (magnesium), mono-, di-, tricalcium (magnesium) citrate, calcium gluconate, calcium carbonate or bicarbonate (magnesium), etc. Acid salts, neutral salts, or basic salts, or alkali metal salts of monocitrate, di,
Sodium (potassium), tartaric acid, fumaric acid, mono- or dipotassium (sodium) of adipic acid, potassium acid metaphosphate (sodium), sodium (potassium) pyrophosphate, acid salts of inorganic acids and organic acids such as potassium monophosphate, As a neutral salt, basic salt, ammonium or aluminum salt, it gradually hydrolyzes in water like monoammonium phosphate, dehydrated and dried ammonium alum, alum or glucono delta lactone to become an acidic substance. You may use together.

添加量は、微粒子のジェランガムと金属イオン封鎖剤
の混合物100部に対して1〜300部が望ましい。もちろ
ん、この範囲に限定されるものではない。
The addition amount is desirably 1 to 300 parts with respect to 100 parts of the mixture of the fine particle gellan gum and the sequestering agent. Of course, it is not limited to this range.

その他、たとえ水に可溶性の金属塩であってもその粒
径を大きくするか、これら金属塩の表面を難溶性の物質
で被覆し、溶解速度をおくらせてもよい。金属塩と微粒
子のジェランガムと金属イオン封鎖剤との混合物に常水
又は、冷水を加えて30〜60秒攪拌することによって瞬時
に増粘、ゲル化するもの(速効型)、徐々にゲル化する
もの(遅効型)が得られる。これらの増粘、ゲル化の速
度は、選択する金属塩類及びその添加割合によって自由
に調整出来る。なお、グルコノデルタラクトンを添加し
た場合は遅効性となる。
In addition, even if the metal salt is soluble in water, the particle size may be increased, or the surface of the metal salt may be coated with a hardly soluble substance to increase the dissolution rate. A mixture of gellan gum, a metal salt, fine particles of gellan and a sequestering agent, added with ordinary water or cold water and stirred for 30 to 60 seconds to instantaneously thicken and gel (rapid-effect type), and gradually gel Stuff (slow effect) is obtained. The rate of these thickening and gelling can be freely adjusted by the selected metal salts and the ratio of addition. In addition, when glucono delta lactone is added, it has a delayed effect.

更に、微粒子のジェランガムと金属イオン封鎖剤の混
合物に水を加えて溶解し、得られた水溶液にアルカリ金
属塩、アルカリ土類金属塩、アンモニウム、アルミニウ
ム塩の無機塩、有機酸又は酸性塩、中性塩、塩基性塩を
加えてもよく、あるいはこれを含む物質、例えば炭酸飲
料、コーヒー、紅茶、牛乳、果汁、ワイン、日本酒、ブ
ランデー、ヨーグルト、アセロラ果汁、その他を添加、
混合することによっても同様に即席増粘ゲル化物が得ら
れる。
Further, water is added to and dissolved in a mixture of the particulate gellan gum and the sequestering agent, and the resulting aqueous solution is treated with an alkali metal salt, an alkaline earth metal salt, ammonium, an inorganic salt of an aluminum salt, an organic acid or an acid salt, Basic salts, basic salts may be added, or substances containing the same, such as carbonated beverages, coffee, tea, milk, juice, wine, sake, brandy, yogurt, acerola juice, etc.
By mixing, an instantly thickened gelled substance can be obtained.

〔発明の効果〕〔The invention's effect〕

以下にこの発明の効果を実験例をもって証明する。 Hereinafter, the effects of the present invention will be proved by experimental examples.

実験例1 常水を攪拌しながら下記の安定剤を添加、30〜60秒間
攪拌溶解後、冷蔵庫内(5℃)にて1時間冷却した。
Experimental Example 1 The following stabilizer was added while stirring normal water, and dissolved by stirring for 30 to 60 seconds, followed by cooling in a refrigerator (5 ° C.) for 1 hour.

粘度:B型回転粘度計使用 ローター#2 回転数60rpm ゲル強度:飯尾電気(株)モデル301型にて測定した。Viscosity: using a B-type rotational viscometer Rotor # 2 Rotational speed 60 rpm Gel strength: Measured with a model 301 of Iio Electric Co., Ltd.

実施例1 ジェランガムをボールミルにて粉砕し、粒子径を75μ
mにした微粒子のジェランガム0.4部とメタリン酸ナト
リウム0.1部を水(10℃)100部に加え、30秒間攪拌した
ところ透明な粘稠のある溶液となった。この時の粘度は
240cpsであった。
Example 1 Gellan gum was pulverized with a ball mill to a particle size of 75 μm.
0.4 parts of gellan gum and 0.1 part of sodium metaphosphate were added to 100 parts of water (10 ° C.) and stirred for 30 seconds to form a transparent viscous solution. The viscosity at this time is
240 cps.

対照品としてジェランガム0.4部、メタリン酸ナトリ
ウム0.1部を水(10℃)100部に加え、30秒間攪拌したと
ころ、ジェランガムの不溶解粒子が懸濁し白濁した液と
なった。この水溶液の粘度は15cpsであった。以上の結
果、本発明の微粒子のジェランガムは容易に水(10℃)
に溶解することがわかった。
As a control, 0.4 part of gellan gum and 0.1 part of sodium metaphosphate were added to 100 parts of water (10 ° C.), and the mixture was stirred for 30 seconds. As a result, insoluble particles of gellan gum were suspended to form a cloudy liquid. The viscosity of this aqueous solution was 15 cps. As a result, the fine gellan gum of the present invention can be easily dissolved in water (10 ° C).
It was found to dissolve in.

又、メタリン酸ナトリウムの代りにフィチン酸、クエ
ン酸ナトリウムを使用しても同様の結果が得られた。
Similar results were obtained when phytic acid and sodium citrate were used instead of sodium metaphosphate.

実施例2 微粒子のジェランガム0.4部、メタリン酸ナトリウム
0.1部に硫酸カルシウム0.05部を混合ししたものを水(1
0℃)100部に加え30秒間攪拌し、25℃で5分間放置した
ところゲル化した。このときのゲル強度は、ブルームゲ
ロメーターで測定したとき200ブルームであった。一
方、実施例1の対照品と硫酸カルシウム0.05部を水(10
℃)100部に加え攪拌したがゲル化しなかった。
Example 2 Fine Particulate Gellan Gum 0.4 Part, Sodium Metaphosphate
A mixture of 0.1 part of 0.05 part of calcium sulfate mixed with water (1
(0 ° C.) and stirred for 30 seconds. The mixture was left at 25 ° C. for 5 minutes to gel. The gel strength at this time was 200 bloom when measured by a bloom gelometer. On the other hand, 0.05 part of calcium sulfate and water (10
° C) and stirred, but did not gel.

実施例3 微粒子のジェランガム0.4部、メタリン酸ナトリウム
0.1部にグルコノデルタラクトン0.2部を混合したものを
水(10℃)100部に加え、30秒間攪拌し、25℃で30分間
放置したところ、透明なゲルが出来た。このときのゲル
強度は175ブルームであった。
Example 3 Fine Particulate Gellan Gum 0.4 Part, Sodium Metaphosphate
A mixture of 0.1 part of glucono delta lactone and 0.2 part of glucono delta lactone was added to 100 parts of water (10 ° C.), stirred for 30 seconds, and left at 25 ° C. for 30 minutes to form a transparent gel. The gel strength at this time was 175 bloom.

実施例4 微粒子のジェランガム0.4部、メタリン酸ナトリウム
0.1部を水(10℃)100部に加え30秒間攪拌、溶解した液
に果汁10部、牛乳30部、日本酒20部、ワイン20部、ブラ
ンデー20部、クエン酸0.1部を加え10秒間混和したとこ
ろゲル化した。
Example 4 0.4 parts of fine gellan gum, sodium metaphosphate
0.1 part was added to 100 parts of water (10 ° C.) and stirred for 30 seconds. To the dissolved liquid, 10 parts of fruit juice, 30 parts of milk, 20 parts of sake, 20 parts of wine, 20 parts of brandy, and 0.1 part of citric acid were added and mixed for 10 seconds. However, it gelled.

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】微粒子のジェランガムに金属イオン封鎖剤
を含むことを特徴とする即席増粘ゲル化物の製造方法。
1. A method for producing an instantly thickened gelled substance, comprising a fine particle gellan gum containing a sequestering agent.
【請求項2】特許請求の範囲第1項に記載の即席増粘ゲ
ル化物に金属塩及び又は、グルコノデルタラクトンを併
用することを特徴とする即席増粘ゲル化物の製造方法。
2. A method for producing an instantly thickened gelled product, which comprises using a metal salt and / or glucono-delta-lactone in combination with the instantly thickened gelled product according to claim 1.
【請求項3】特許請求の範囲第1項に記載の水溶液に金
属塩及び又は、有機酸、無機酸あるいは金属塩及び又
は、有機酸、無機酸を含む物質を加えることを特徴とす
る即席増粘ゲル化物の製造方法。
3. An aqueous solution according to claim 1, wherein a metal salt and / or an organic acid, an inorganic acid or a substance containing a metal salt and / or an organic acid or an inorganic acid is added to the aqueous solution. A method for producing a viscous gel.
JP63167528A 1988-07-05 1988-07-05 Method for producing instant thickened gelled product Expired - Lifetime JP2731397B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63167528A JP2731397B2 (en) 1988-07-05 1988-07-05 Method for producing instant thickened gelled product

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63167528A JP2731397B2 (en) 1988-07-05 1988-07-05 Method for producing instant thickened gelled product

Publications (2)

Publication Number Publication Date
JPH0218487A JPH0218487A (en) 1990-01-22
JP2731397B2 true JP2731397B2 (en) 1998-03-25

Family

ID=15851366

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63167528A Expired - Lifetime JP2731397B2 (en) 1988-07-05 1988-07-05 Method for producing instant thickened gelled product

Country Status (1)

Country Link
JP (1) JP2731397B2 (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2191350A1 (en) * 1994-06-24 1996-01-04 William Fritsche Chalupa Gellan gum beverage
AU5955496A (en) * 1995-06-06 1996-12-24 Nutrasweet Company, The Dry mix texture modified beverage using gellan gum
US5641532A (en) * 1995-12-15 1997-06-24 The Procter & Gamble Company Beverages having stable flavor/cloud emulsions in the presence of polyphosphate-containing preservative systems by including gellan gum
JP2000245362A (en) * 1999-03-03 2000-09-12 House Foods Corp Jelly food and its production
KR20010102550A (en) * 2000-01-11 2001-11-15 겜마 아키라 Microgels and external preparations containing the same
JP2007222041A (en) * 2006-02-22 2007-09-06 Sunnyhealth Co Ltd Method for producing meat or fish processed food
JP2011000051A (en) * 2009-06-18 2011-01-06 Sanei Gen Ffi Inc Liquid base for preparing instant dessert

Also Published As

Publication number Publication date
JPH0218487A (en) 1990-01-22

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