JPS5910178B2 - Caramel refining method - Google Patents

Caramel refining method

Info

Publication number
JPS5910178B2
JPS5910178B2 JP51065334A JP6533476A JPS5910178B2 JP S5910178 B2 JPS5910178 B2 JP S5910178B2 JP 51065334 A JP51065334 A JP 51065334A JP 6533476 A JP6533476 A JP 6533476A JP S5910178 B2 JPS5910178 B2 JP S5910178B2
Authority
JP
Japan
Prior art keywords
caramel
membrane
molecular weight
weight cutoff
reverse osmosis
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
Application number
JP51065334A
Other languages
Japanese (ja)
Other versions
JPS52148665A (en
Inventor
安弘 坂口
克己 小島
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.)
Daicel Corp
Original Assignee
Daicel Chemical Industries 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 Daicel Chemical Industries Ltd filed Critical Daicel Chemical Industries Ltd
Priority to JP51065334A priority Critical patent/JPS5910178B2/en
Publication of JPS52148665A publication Critical patent/JPS52148665A/en
Publication of JPS5910178B2 publication Critical patent/JPS5910178B2/en
Expired legal-status Critical Current

Links

Landscapes

  • Coloring Foods And Improving Nutritive Qualities (AREA)

Description

【発明の詳細な説明】 本発明は、膜分離法による食用カラメルの精製法に係る
ものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for purifying edible caramel using a membrane separation method.

一般に食用カラメル着色剤は、糖類の溶液に酸、アルカ
リ、塩類などの触媒を加えて加熱焙焼して製造される。
Edible caramel colorants are generally produced by adding a catalyst such as an acid, an alkali, or a salt to a sugar solution and then heating and roasting the mixture.

例えば触媒として亜硫酸塩類(ナトリウム塩、カリウム
塩、アンモニウム塩)を使用する場合、原料糖液に対し
て10〜35%もの亜硫酸塩を添加し110〜140℃
に加熱してカラメルを製造するが、その場合多量の亜硫
酸塩が使用されているので製品中に亜硫酸ガスが多量に
残存する欠点がある。
For example, when using sulfites (sodium salt, potassium salt, ammonium salt) as a catalyst, 10-35% sulfite is added to the raw sugar solution and the temperature is raised to 110-140℃.
However, since a large amount of sulfite is used in this case, there is a drawback that a large amount of sulfur dioxide gas remains in the product.

これらの残存亜硫酸ガスを除去する方法としては、陰イ
オン交換樹脂による方法、酸化剤処理法、加圧加熱放圧
処理法があるが亜硫酸ガスの除去効率は未だ十分ではな
かった。
Methods for removing these residual sulfur dioxide gases include a method using an anion exchange resin, an oxidizing agent treatment method, and a pressure heating and pressure release treatment method, but the removal efficiency of sulfur dioxide gas has not yet been sufficient.

本発明は、この欠点を改良するため逆浸透膜又は限外f
過膜を用いる膜分離法でカラメル中の亜髄酸塩を除去す
るものである。
In order to improve this drawback, the present invention proposes a reverse osmosis membrane or an ultra-f
This method uses a membrane separation method to remove myelite from caramel.

本発明の方法によると、例えば分画分子量1000〜5
000の限外沢過膜を用い効率的にカラメル中の亜硫酸
塩を除去でき、又、同時に着色物質中に含まれる不純物
としての低分子量のりプリン酸などの有機酸、アルコー
ル、エステル類などを除去でき、カラメル品質を向上さ
せることができる。
According to the method of the present invention, for example, a molecular weight cutoff of 1000 to 5
000 ultrafiltration membrane can be used to efficiently remove sulfites in caramel, and at the same time remove organic acids such as low molecular weight glue puric acid, alcohol, esters, etc. as impurities contained in coloring substances. It can improve caramel quality.

更に又、本発明の方法によると膜分離法の特徴である分
両性を利用して、同一原料から得られるカラメル着色剤
を色相の異なる数種の色相グループに分別分離すること
ができる。
Furthermore, according to the method of the present invention, the caramel coloring agent obtained from the same raw material can be separated into several hue groups having different hues by utilizing the amphoteric nature that is a feature of the membrane separation method.

即ち、一般には糖質の種類、pHの調整、アンモニア、
アンモニウム塩、アミノ酸、アルカリ性ナトリウム化合
物の添加、加熱条件(温度:時間)等により色調や性状
が異なるものが作られるが、本発明では、糖質の種類を
変えずに同一原料から色調や性状の異なるものが得られ
た。
That is, in general, the type of carbohydrate, pH adjustment, ammonia,
Products with different colors and properties can be produced depending on the addition of ammonium salts, amino acids, alkaline sodium compounds, heating conditions (temperature: time), etc., but in the present invention, products with different colors and properties can be made from the same raw material without changing the type of carbohydrate. I got something different.

例えば、カラメル着色剤を分画分子量40000以上(
ダイセル製アクリロニトリルコポリマー系限外p過膜D
UY−40)、20000以上(DUY−20)、10
000以上(DUY−10)、5000以上(DUY−
05 )、1000以上(酢酸セルロース系限外沢過膜
、DUC−01)、500以上(酢酸セルロース系逆浸
透膜、DBS−0)の順に分画することにより同一糖質
から成分組成の均一な着色度の黒褐色から淡黄色に至る
色相が異なる6種のグループに分別され醤油用からコー
ラ、レモンに至る各種着色剤に使用することができる。
For example, use a caramel colorant with a molecular weight cut-off of 40,000 or more (
Acrylonitrile copolymer ultrap membrane D manufactured by Daicel
UY-40), 20000 or more (DUY-20), 10
000 or more (DUY-10), 5000 or more (DUY-
05), 1,000 or more (cellulose acetate ultrafiltration membrane, DUC-01), and 500 or more (cellulose acetate reverse osmosis membrane, DBS-0) to obtain homogeneous composition from the same carbohydrate. It is classified into six groups with different hues ranging from dark brown to pale yellow, and can be used in various coloring agents from soy sauce to cola and lemon.

以下実施例により説明する。This will be explained below using examples.

実施例 1 精製葡萄糖5kgを1 5 0 0dの純水に溶解し、
720tの亜硫酸ナトリウムを加えオートクレープ中で
120℃で3時間加熱し液状カラメル7220yを得た
Example 1 5 kg of purified glucose was dissolved in 1500 d of pure water,
720t of sodium sulfite was added and heated in an autoclave at 120°C for 3 hours to obtain liquid caramel 7220y.

この液を2倍に稀釈し、ダイセル製内圧式管状型限外沢
過装置(管径14.5φ、長さ75crrL、使用膜酢
酸セルロース系限外沢過膜DUC −0 1 、圧力7
kg/cd、温度45℃、流速2m/sec、膜面積
0.277j)を用い、減容比率を1/2まで限外沢過
処理を行い表1の性状のカラメルを得た。
This solution was diluted twice and diluted with an internal pressure tubular type ultrafiltration device manufactured by Daicel (tube diameter 14.5φ, length 75 crrL, membrane used: cellulose acetate ultrafiltration membrane DUC-0 1, pressure 7).
kg/cd, temperature 45° C., flow rate 2 m/sec, membrane area 0.277 j), ultrafiltration treatment was performed to reduce the volume reduction ratio to 1/2, and caramel having the properties shown in Table 1 was obtained.

尚、参考までに逆浸透法処理の行わない原液、性状を対
比した。
For reference, the properties of the stock solution without reverse osmosis treatment were compared.

表1に示した様に本方法によると残存亜硫酸ガ・スは、
1 0 ppm以下となり食品許容範囲30ppm以内
でかつ少量残存する有機酸やアルコールなど不純物を含
有しない良質の精製カラメルを得ることができた。
As shown in Table 1, according to this method, residual sulfite gas is
It was possible to obtain a high-quality purified caramel which had a concentration of 10 ppm or less, which was within the food tolerance range of 30 ppm, and which did not contain a small amount of impurities such as residual organic acid or alcohol.

実施例 2 水飴2kgを6000rIllの純水に溶解し1.4モ
ル炭酸カリウム、0.6モルの炭酸水素カリウム、4規
定の水酸化ナトリウムの混合液による緩衝液を用いpH
10に調製し125℃、60分加熱反応させカラメル
を製造した。
Example 2 2 kg of starch syrup was dissolved in 6000 ml of pure water, and the pH was adjusted using a buffer solution containing a mixture of 1.4 mol potassium carbonate, 0.6 mol potassium bicarbonate, and 4N sodium hydroxide.
10 and heated and reacted at 125° C. for 60 minutes to produce caramel.

得られたカラメルを実施例1と同一の限外F過装置を用
い、最初に原液を2倍に稀釈し分画分子量40000の
DUY−40膜を用い減容比1/2まで限外F過し、そ
の透過処理液を分画分子量iooooのDUY−10膜
を用い減容比1/2まで限外沢過し、その処理液を分画
分子量500の逆浸透膜DBS−0を用い逆浸透法処理
し、4kgのカラメル液を得た。
Using the same ultra-F filtration apparatus as in Example 1, the obtained caramel was first diluted to 2 times the stock solution and ultra-F filtrated to a volume reduction ratio of 1/2 using a DUY-40 membrane with a molecular weight cutoff of 40,000. Then, the permeation treatment liquid was subjected to ultrafiltration to a volume reduction ratio of 1/2 using a DUY-10 membrane with a molecular weight cutoff of iooooo, and the treated liquid was subjected to reverse osmosis using a reverse osmosis membrane DBS-0 with a molecular weight cutoff of 500. Processing was performed to obtain 4 kg of caramel liquid.

得られたカラメルの性状は表2の通りであった。The properties of the obtained caramel were as shown in Table 2.

表2の結果から、カラメルを膜分離処理することにより
カラメルの実用的性状を余り変えることな《色調を顕著
に変え、コーラ用、醤油用、ミート用、レモン用などの
特殊用途に使用することができた。
From the results in Table 2, membrane separation treatment of caramel does not significantly change the practical properties of caramel (it significantly changes the color tone and can be used for special purposes such as cola, soy sauce, meat, and lemon). was completed.

Claims (1)

【特許請求の範囲】 1 カラメル着色剤中の不純物を除去精製するに当り逆
浸透膜又は限外沢過膜を用いて処理することを特徴とす
るカラメルの精製法。 2 分画分子量1000〜5000の限外f過膜を用い
る特許請求の範囲第1項記載の精製法。 3 分画分子量40000乃至500の逆浸透膜又は限
外沢過膜を、分画分子量の大きい膜から小さい膜へ逐次
段階的に用いて分別する特許請求の範囲第1項記載の精
製法。
[Scope of Claims] 1. A method for purifying caramel, which comprises using a reverse osmosis membrane or an ultrafiltration membrane to purify and remove impurities from a caramel colorant. 2. The purification method according to claim 1, which uses an ultraf membrane having a molecular weight cutoff of 1000 to 5000. 3. The purification method according to claim 1, wherein a reverse osmosis membrane or an ultrafiltration membrane having a molecular weight cutoff of 40,000 to 500 is used for fractionation in a stepwise manner from a membrane with a higher molecular weight cutoff to a membrane with a lower molecular weight cutoff.
JP51065334A 1976-06-04 1976-06-04 Caramel refining method Expired JPS5910178B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP51065334A JPS5910178B2 (en) 1976-06-04 1976-06-04 Caramel refining method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP51065334A JPS5910178B2 (en) 1976-06-04 1976-06-04 Caramel refining method

Publications (2)

Publication Number Publication Date
JPS52148665A JPS52148665A (en) 1977-12-10
JPS5910178B2 true JPS5910178B2 (en) 1984-03-07

Family

ID=13283910

Family Applications (1)

Application Number Title Priority Date Filing Date
JP51065334A Expired JPS5910178B2 (en) 1976-06-04 1976-06-04 Caramel refining method

Country Status (1)

Country Link
JP (1) JPS5910178B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62113473U (en) * 1985-12-30 1987-07-18

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110244102A1 (en) * 2010-03-30 2011-10-06 Pepsico, Inc. Removal Of Reaction Byproducts And Impurities From Caramel Color And A Shelf Stable Caramel Color Concentrate
US20110250338A1 (en) * 2010-04-08 2011-10-13 Pepsico., Inc. Adsorption Purification Of Caramel
MY177579A (en) * 2014-06-18 2020-09-21 Coca Cola Co Method for reducing low molecular weight species in caramel
KR102566245B1 (en) * 2016-09-20 2023-08-11 더 코카콜라 컴파니 edible caramel color composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62113473U (en) * 1985-12-30 1987-07-18

Also Published As

Publication number Publication date
JPS52148665A (en) 1977-12-10

Similar Documents

Publication Publication Date Title
JP2749120B2 (en) Purification of polydextrose by reverse osmosis
JPS5828246A (en) Preparation of stevioside
JPS5828247A (en) Purifying method of stevioside solution
JP2630857B2 (en) Cigarette paper colorant
JP2013523127A (en) Removal of reaction by-products and impurities from caramel color and caramel color concentrate that can be stored at room temperature for a long time
AU2011238746A1 (en) Adsorption purification of caramel
JPS5910178B2 (en) Caramel refining method
JP4768142B2 (en) Simple manufacturing method of fucoidan
JP3617091B2 (en) Purification method of basic amino acids
JPS6332427B2 (en)
JPS6240261A (en) Decoloration of liquid food
JP2739704B2 (en) Liquid papain composition for adding food and drink
JPS58164601A (en) Production of water-soluble chitosan salt
JP2762087B2 (en) Decolorization method for liquid food
JPH02113859A (en) Production of protein hydrolyzate
JPH01215293A (en) Separation and recovery of erythritol
CN111171139A (en) Elastin and synthetic method thereof
SU1565878A1 (en) Method of production of "stolichnaya krystall" vodka
SU1684330A1 (en) Method of producing "privet" vodka
RU1838398C (en) Method for producing vodka
RU2139294C1 (en) Method of preparing hydroxyethylated starch
JPH07222570A (en) Production of thick soup stock
SU589956A1 (en) Method of purifying agar solutions from admixtures
AU3823195A (en) Process for recovering citric acid
JPH03200765A (en) Method for purifying l-tryptophan