JPH0480665B2 - - Google Patents
Info
- Publication number
- JPH0480665B2 JPH0480665B2 JP59033113A JP3311384A JPH0480665B2 JP H0480665 B2 JPH0480665 B2 JP H0480665B2 JP 59033113 A JP59033113 A JP 59033113A JP 3311384 A JP3311384 A JP 3311384A JP H0480665 B2 JPH0480665 B2 JP H0480665B2
- Authority
- JP
- Japan
- Prior art keywords
- oil
- oil agent
- pigment
- extraction
- raw 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.)
- Expired - Lifetime
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/54—Improvements relating to the production of bulk chemicals using solvents, e.g. supercritical solvents or ionic liquids
Landscapes
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Extraction Or Liquid Replacement (AREA)
Description
【発明の詳細な説明】
この発明は、色素に係るものであり、品質の優
れた食用色素を工業的に有利に収得することを目
的とする。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to pigments and aims to industrially advantageously obtain food pigments of excellent quality.
食用色素は、水溶性のものと、油溶性のものと
に二大別される。この発明は後者即ち親油性の色
素に係るものである。 Food coloring is divided into two types: water-soluble and oil-soluble. This invention relates to the latter, that is, lipophilic dyes.
親油性色素の収得法としては、油剤抽出法、水
蒸気蒸溜法等があるが、いずれの方法も重大な欠
点をもつている。欠点としては例えば、製品の収
得歩留りが低い、夾雑物の除去割合が低い、時と
して対象の色素の変化が起こる、その他である。
これ等は使用する温度が高過ぎたり、処理時間が
長い等を主原因とするとみられる。この発明は、
このような欠点のないものであり、以下にこの発
明を説明する。 Methods for obtaining lipophilic pigments include oil extraction methods and steam distillation methods, but each method has serious drawbacks. Disadvantages include, for example, low product yields, low contaminant removal rates, and sometimes changes in the target pigment, among others.
The main causes of this seem to be that the temperature used is too high or the processing time is long. This invention is
This invention is free from these drawbacks and will be described below.
対象の色素原料は、親油性色素を含むもの一般
である。このような色素としては、例えば、カロ
チノイド系、ジケトン系、ポルフイリン系、その
他のものが挙げられる。このようなのとしては、
植物の種実、葉、莖、根、魚貝類その他がある。
これ等は、単種でまたは2種以上合せて処理され
る。 The target dye raw materials are generally those containing lipophilic dyes. Examples of such pigments include carotenoids, diketones, porphyrins, and others. As such,
Plant seeds, leaves, pods, roots, fish and shellfish, etc.
These can be treated singly or in combination.
つぎに色素の収得の工程を説明する。 Next, the process of obtaining the dye will be explained.
親油性色素を含む原料、例えば、カロチノイド
を含むアナトー、パプリカ等の原料を用意し、こ
れとこれ等の色素を溶解保持する能力のある油
剤、例えばヘキサン、アセトン、または精製ヤシ
油からなる群から選ばれた1種以上を接触させ均
質混合系を作り、原料中の色素を油剤中に移行さ
せる。この工程は抽出タンク内で行われる。これ
に、炭酸ガス、エチレン、プロパン等を圧入し、
これを臨界温度・圧力以上の状態にする。このよ
うにすると、色素を含有する油剤は、抽出相に移
行するから、この抽出相を分離タンクに導き、減
圧または温度変化により抽出成分は炭酸ガス等の
抽出剤より分離する。このようにすると、色素を
溶解保持する油剤が得られる。この際、収得物
中、色素の濃度の高いものを要するときは、当該
油剤の使用量を少なくするか、分離タンクでの条
件を調節して添加油剤の一部を分別除去すれば良
い。更に原料中の異味・異臭成分は、その大部分
が当該油剤の沸点よりも低い沸点の物質であるか
ら、前記色素を溶解保持する油剤には含有され
ず、分離タンクの気相部に存在する。また、蛋白
質、でん粉、繊維質等は抽出されず抽出タンク内
に残留する。分離タンク中に生成するペースト状
ないし液状物がこの発明の目的物である。ここ
に、この発明はその目的を達し終える。 A raw material containing a lipophilic pigment, for example, a raw material such as annatto or paprika containing carotenoids is prepared, and an oil agent capable of dissolving and retaining these pigments, such as hexane, acetone, or refined coconut oil, is prepared. One or more selected species are brought into contact to create a homogeneous mixed system, and the pigments in the raw materials are transferred into the oil agent. This process takes place in an extraction tank. Carbon dioxide, ethylene, propane, etc. are press-fitted into this,
This is brought to a state above the critical temperature and pressure. In this way, since the oil containing the pigment is transferred to the extraction phase, this extraction phase is introduced into a separation tank, and the extracted components are separated from the extractant such as carbon dioxide gas by reducing the pressure or changing the temperature. In this way, an oil agent that dissolves and retains the pigment can be obtained. At this time, if a product with a high pigment concentration is required among the obtained products, the amount of the oil agent used may be reduced or the conditions in the separation tank may be adjusted to separate and remove a portion of the added oil agent. Furthermore, most of the off-taste and odor components in the raw materials are substances with boiling points lower than the boiling point of the oil, so they are not contained in the oil that dissolves and retains the pigment, but are present in the gas phase of the separation tank. . In addition, proteins, starches, fibers, etc. are not extracted and remain in the extraction tank. The paste-like or liquid material produced in the separation tank is the object of this invention. Here, the invention has achieved its purpose.
この発明の作用及び効果の若干を以下に説明す
ると、収得色素は、収得率が高く、かつ変色が
ほとんどない。色素の変色温度以下の温度におい
て処理することができるからである。油剤およ
び抽剤は反覆使用することができるから、損耗率
が極めて小さい。製造工程が簡易である。 Some of the functions and effects of this invention will be explained below. The obtained dye has a high yield and has almost no discoloration. This is because the treatment can be performed at a temperature below the discoloration temperature of the dye. Since the oil and extractant can be used repeatedly, the rate of wear and tear is extremely low. The manufacturing process is simple.
この発明を、以下に実施例により説明する。 This invention will be explained below by way of examples.
実施例 1
キヤロツトオレオレンジン500gを用意し、こ
れと精製ヤシ油とを抽出タンクに仕込み均質混合
系を作り原料中の色素を精製ヤシ油に溶出させ
た。ついで炭酸ガスを圧入して外部加熱し、抽出
タンク内部を超臨界状態にした。抽出タンクか
ら、原料中の揮発分、油脂分、油剤が抽出相とし
て分離タンクに移行し、抽出タンク内部に繊維
質、でん紛質、蛋白質が残つた。分離タンクを減
圧したところ着色した液状油剤層が生成した。液
状油剤層をタンクから外部に取出して、キヤロツ
トーのヤシ油溶液2.50gを得た。この色素液を室
内に3カ月間放置したが、異味・異臭がなく、変
色も起らなかつた。Example 1 500 g of carrot oleorangein was prepared, and this and refined coconut oil were charged into an extraction tank to create a homogeneous mixing system, and the pigment in the raw material was eluted into the refined coconut oil. Next, carbon dioxide gas was injected and external heating was performed to bring the inside of the extraction tank into a supercritical state. From the extraction tank, the volatile components, fats and oils in the raw materials were transferred to the separation tank as the extraction phase, and fibers, starch, and proteins remained inside the extraction tank. When the separation tank was depressurized, a colored liquid oil layer was produced. The liquid oil layer was taken out from the tank to obtain 2.50 g of coconut oil solution. This dye solution was left indoors for three months, but there was no strange taste or odor, and no discoloration occurred.
実施例 2
粗トマトパウダー1Kg(リコピン180mg%含有)
とヘキサン2とを抽出タンクに仕込み均質混合
系を作り原料中の色素をヘキサンに溶出させる。
ついで、超臨界炭酸ガスを接触させた。この時の
条件は、35〜50℃/300Kg/cm2で行ない、色素の
回収は減圧法で行なつた。分離タンクには、約
200gの精製リコピン色素(リコピン1370mg%含
有)が得られた。Example 2 Crude tomato powder 1Kg (contains 180mg% lycopene)
and hexane 2 are charged into an extraction tank to create a homogeneous mixed system, and the pigment in the raw material is eluted into hexane.
Then, supercritical carbon dioxide gas was brought into contact. The conditions at this time were 35-50° C./300 Kg/cm 2 , and the dye was recovered by a reduced pressure method. The separation tank contains approx.
200 g of purified lycopene pigment (containing 1370 mg% lycopene) was obtained.
収得したリコピンは臭気がほとんどなく、油に
着色した際非常に鮮明な橙色を呈した。また、こ
のリコピンは、15℃1カ月放置して異味・異臭の
発生がなく変色もなかつた。 The obtained lycopene had almost no odor and exhibited a very vivid orange color when colored into oil. Furthermore, this lycopene did not develop any strange taste or odor and did not change color after being left at 15°C for one month.
Claims (1)
油剤を接触させ、原料中の色素を油剤中に移行さ
せ、均質系とし、これに炭酸ガス、エチレンまた
はプロパンから選ばれた少なくとも1種を添加
し、これを超臨界状態にして抽出を行い、抽出相
から色素成分を分離することを特徴とする親油性
食用色素の製造法。 2 食用色素が、カロチノイド系、ジケトン系、
ポルフイリン系からなる群から選ばれた少なくと
も1種である請求項1記載の製造法。 3 油剤がヘキサン、アセトン、または精製ヤシ
油からなる群から選ばれた少なくとも1種である
請求項1記載の製造法。[Claims] 1. A raw material containing lipophilic and non-hydrophilic food coloring,
Bringing into contact with an oil agent, the pigment in the raw material is transferred into the oil agent to form a homogeneous system, and at least one selected from carbon dioxide gas, ethylene, or propane is added to this, and the mixture is brought into a supercritical state for extraction. A method for producing lipophilic food coloring, which is characterized by separating a coloring component from an extraction phase. 2 The food coloring is carotenoid-based, diketone-based,
2. The method according to claim 1, wherein the porphyrin is at least one selected from the group consisting of porphyrins. 3. The production method according to claim 1, wherein the oil agent is at least one selected from the group consisting of hexane, acetone, and refined coconut oil.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59033113A JPS60176563A (en) | 1984-02-22 | 1984-02-22 | Production of oleophilic food dye |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59033113A JPS60176563A (en) | 1984-02-22 | 1984-02-22 | Production of oleophilic food dye |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60176563A JPS60176563A (en) | 1985-09-10 |
| JPH0480665B2 true JPH0480665B2 (en) | 1992-12-21 |
Family
ID=12377591
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59033113A Granted JPS60176563A (en) | 1984-02-22 | 1984-02-22 | Production of oleophilic food dye |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60176563A (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6336803A (en) * | 1986-07-31 | 1988-02-17 | Seitetsu Kagaku Co Ltd | Treatment of expandable material |
| JPH01123864A (en) * | 1987-11-09 | 1989-05-16 | Mori Seiyu Kk | Separation of dye oleoresin and spice oleoresin by extraction |
| JPH04144664A (en) * | 1990-10-05 | 1992-05-19 | Mori Seiyu Kk | Extractive production of pungent component and red dyestuff component of red pepper |
| DE4429506B4 (en) * | 1994-08-19 | 2007-09-13 | Degussa Gmbh | Process for the extraction of natural carotenoid dyes |
| ITBA20060049A1 (en) * | 2006-08-02 | 2008-02-03 | Pierre S R L | FOOD SUPPLEMENT BASED ON BIOLOGICAL LYCOPENE AND PROCEDURE FOR OBTAINING BIOLOGICAL LICOPENE. |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE7410542L (en) * | 1974-01-29 | 1976-01-12 | Givaudan & Cie Sa | CONDENSATION PRODUCTS. |
| DE3114593C1 (en) * | 1981-04-10 | 1982-12-09 | Fried. Krupp Gmbh, 4300 Essen | Process for the extraction of flavorings and colors from paprika |
| JPS58173163A (en) * | 1982-04-05 | 1983-10-12 | San Ei Chem Ind Ltd | Production of carotenoid coloring matter |
-
1984
- 1984-02-22 JP JP59033113A patent/JPS60176563A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60176563A (en) | 1985-09-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE4429506B4 (en) | Process for the extraction of natural carotenoid dyes | |
| EP1857441B1 (en) | Method of separating and purifying xanthophyll fatty acid esters from marigold oleoresin | |
| KR920005369B1 (en) | Process for making antioxidant composition having herb flavoring | |
| US8425948B2 (en) | Process for isolation of lutein and zeaxanthin crystals from plant sources | |
| JP2003201497A (en) | Method for producing lutein fatty acid ester concentrate | |
| DE60313096T2 (en) | Process for the purification of Marigold oleoresin | |
| DE19531254A1 (en) | Process for the extraction of carotene dyes from solid natural substances | |
| JP2005532048A (en) | Novel trans-lutein rich xanthophyll ester concentrate and process for its preparation | |
| JPH0480665B2 (en) | ||
| KR20180097505A (en) | A novel organic solubilization and / or extraction solvent, an extraction method using the solvent, and an extract obtained by the method | |
| EP0062893A1 (en) | Process for producing plant extracts with sensory properties | |
| JP2000063827A (en) | Method for producing antioxidant | |
| JPH06113872A (en) | New manufacturing method of chlorophyll composition | |
| EP1270710A1 (en) | A method of processing lipid materials | |
| DE2000689A1 (en) | Process for extraction treatment of hops | |
| AU2001294049B2 (en) | Extraction method | |
| JPH0119826B2 (en) | ||
| JPS5934736B2 (en) | Manufacturing method of paprika pigment | |
| JPH09157537A (en) | Deodorizing purification method of pigment | |
| JP5864042B2 (en) | Process for producing a food material comprising an extract containing β-cryptoxanthin | |
| US2615813A (en) | Process for decolorizing and sterilizing spices | |
| CN108218821B (en) | Method for extracting and purifying anthocyanin from acorn shells | |
| JPH0448420B2 (en) | ||
| JPH0258576A (en) | Edible natural pigment | |
| JP2004131496A (en) | Purification method of marigold oleoresin |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EXPY | Cancellation because of completion of term |