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JPS60133002A - Preparation of pectin - Google Patents

Preparation of pectin

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Publication number
JPS60133002A
JPS60133002A JP58238916A JP23891683A JPS60133002A JP S60133002 A JPS60133002 A JP S60133002A JP 58238916 A JP58238916 A JP 58238916A JP 23891683 A JP23891683 A JP 23891683A JP S60133002 A JPS60133002 A JP S60133002A
Authority
JP
Japan
Prior art keywords
pectin
extract
pressing
concentration
insoluble component
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
JP58238916A
Other languages
Japanese (ja)
Other versions
JPH0643445B2 (en
Inventor
Shiyouji Suzuki
鈴木 晶二
Hirofumi Ninomiya
弘文 二宮
Taku Tabuchi
田渕 卓
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.)
Mitsubishi Acetate Co Ltd
Original Assignee
Mitsubishi Acetate Co Ltd
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Publication date
Application filed by Mitsubishi Acetate Co Ltd filed Critical Mitsubishi Acetate Co Ltd
Priority to JP58238916A priority Critical patent/JPH0643445B2/en
Publication of JPS60133002A publication Critical patent/JPS60133002A/en
Publication of JPH0643445B2 publication Critical patent/JPH0643445B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Jellies, Jams, And Syrups (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)

Abstract

PURPOSE:To obtain pectin useful for jam, etc. efficiently, by blending an extracted solution of pectin with a pressing auxiliary, so that an insoluble component is hardened, pressing is made easy, a channel of pressed solution is kept, and clogging of screen is prevented. CONSTITUTION:An extracted solution obtained from a pectin-containing plant such as lemon, lime, apple, etc. or an insoluble component separated from the extracted solution is blended with >=20pts.wt. pressing auxiliary based on 100 pts.wt. insoluble component, pressed, and the insoluble component is separated to give pectin. Cellulose, sawdust, rice hulls, etc. are used as the pressing auxiliary, and especially effective for hardening the insoluble residue. Diatomaceous earth, perlite, etc. are effective for preventing clogging of screen.

Description

【発明の詳細な説明】 本発明はペクチンの製造方法に関する。[Detailed description of the invention] The present invention relates to a method for producing pectin.

ペクチンは、細胞間の充填並びに組織の支持に役立つ物
質として、植物界一般に広く分布しているコロイド状の
細胞壁多糖類であって、主としてD−ガラクツロン酸の
α−1,4結合より構成され、アラビノース、ガラクト
ース、ラムノース等の中性糖を種々の割合で含有してい
る。
Pectin is a colloidal cell wall polysaccharide that is widely distributed throughout the plant kingdom as a substance that helps fill spaces between cells and support tissues, and is mainly composed of α-1,4 bonds of D-galacturonic acid. It contains various proportions of neutral sugars such as arabinose, galactose, and rhamnose.

特ニレモン、ライム、オレンジ、グレープフルーツ等の
柑橘類の果皮、リンゴ等には良質のペクチンが相当責合
まれ、欧米諸国ではこれらを原料として・ペクチンの製
造がなされている。ペクチン分子中のD−ガラクツロン
酸のカルボキシル基は部分的にメチルエステル化されて
おり、メトキシル化度50%以上のものはハイメトキシ
ル(HM)ペクチン、50%以下のものはロウメトキシ
ル(LM)ペクチシと分類される。これらはそれぞれゲ
ル化の機構やゲル化条件が異なっているが、ペクチンが
低pH系で安定なゲルを形成するという性質、並びに低
pH系で保護コロイド的な働きをするという性質を利用
して、ジャム、ママレード、ゼリー菓子、果汁飲料、ヨ
ーグルト等として食品業界で広く利用されている。
In particular, the peels of citrus fruits such as lemons, limes, oranges, and grapefruits, as well as apples, contain a considerable amount of high-quality pectin, and in Western countries, pectin is manufactured using these as raw materials. The carboxyl group of D-galacturonic acid in pectin molecules is partially methyl esterified, and those with a methoxylation degree of 50% or more are high methoxyl (HM) pectin, and those with a methoxylation degree of less than 50% are low methoxyl (LM) pectin. It is classified as Each of these has different gelation mechanisms and gelation conditions, but pectin forms a stable gel in a low pH system and acts like a protective colloid in a low pH system. It is widely used in the food industry as jam, marmalade, jelly sweets, fruit juice drinks, yogurt, etc.

柑橘類果皮等よりペクチンを製造する一般的な方法は次
のとおりである。果、皮を冷水又は/及び温水で数回洗
浄し、果皮中の糖、有機酸、色素等の水溶性物質を除去
し、次いで塩°酸、硫酸等の無機酸でペクチンを加熱抽
出する。この抽出液を遠心分離、圧搾分離等により不溶
解分を分離し、分離液に珪藻土等の沢過助剤を添加し清
澄f過を行う。得られた沢過液を濃縮してメタノール、
インプロビルアルコール、アセトン等の水混和性有機溶
剤を加えるか、あるいはアルミニウム、銅、鉄等の金属
の塩を添加してペクチンを該金属塩として沈殿させ、脱
水回収する。金属塩法による場合は続いて酸性アルコー
ル等で沈殿を洗浄し、金属分を除去して可溶化させる必
要がある。いずれの場合でも、ペクチンの沈殿を乾燥、
粉砕して粉末ペクチンとする。
A general method for producing pectin from citrus peel etc. is as follows. The fruit and peel are washed several times with cold and/or hot water to remove water-soluble substances such as sugar, organic acids, and pigments in the peel, and then pectin is extracted by heating with an inorganic acid such as hydrochloric acid or sulfuric acid. Undissolved components are separated from this extract by centrifugation, compression, etc., and a filtration aid such as diatomaceous earth is added to the separated solution for clarifying and filtration. The obtained filtrate was concentrated to methanol,
A water-miscible organic solvent such as Improvil alcohol or acetone is added, or a salt of a metal such as aluminum, copper, or iron is added to precipitate pectin as the metal salt, and the pectin is recovered by dehydration. When using the metal salt method, it is necessary to wash the precipitate with acidic alcohol or the like to remove metal components and solubilize them. In either case, dry the pectin precipitate;
Grind into powdered pectin.

このような一般的なペクチンの製造方法における最大の
問題点は、ペクチンの抽出濃度の低さである。乾燥した
ペクチン原料果皮中に含まれるペクチンの割合は原料の
種類、産地、収穫時期等により一定でないが、はぼ10
〜20%程度と言われており、抽出を行った場合、ペク
チン分よりも不溶解の残有部分の方が圧倒的に多い状況
にある。不溶解残有の分離方法として例えば遠心分離を
利用する場合は、分離された残有の固形分濃度が低いた
めに、抽出液の濃度を高くすればするほど分離液の収率
が低下する。
The biggest problem with such general pectin production methods is the low extraction concentration of pectin. The proportion of pectin contained in the dried pectin raw material pericarp varies depending on the type of raw material, production area, harvest time, etc.
It is said to be about ~20%, and when extraction is performed, the undissolved residual portion is overwhelmingly larger than the pectin portion. For example, when centrifugation is used as a method for separating undissolved residuals, the concentration of the separated residual solids is low, so the higher the concentration of the extract, the lower the yield of the separated liquid.

例えば抽出液i度が1%の場合には該分離液の収率が7
5%程度であるのに対し、濃度が1.5%程度になると
分離液の収率は50%程度に低下し、かえって不利な結
果を招く。圧搾法により残有分離を行う場合には、不溶
解分が極めて軟質であるため、ずべりが生じて十分な圧
搾ができず、残有の固形分濃度も上がらず、スクリーン
の目詰まり等を起こしゃすい。
For example, if the degree of extraction liquid is 1%, the yield of the separated liquid is 7.
While it is about 5%, when the concentration is about 1.5%, the yield of the separated liquid decreases to about 50%, which rather brings about disadvantageous results. When separating the residual solids by the squeezing method, the undissolved matter is extremely soft, so it slips and cannot be squeezed sufficiently, and the concentration of the residual solids does not increase, resulting in clogging of the screen, etc. It's easy to wake up.

かかる事情により従来行われているペクチンで の製造方法によれば、ペクチンの濃度限界はせいぜい1
%であり、これより高い場合には不溶解残有分離の困難
さから、かえって効率が低下する。しかし低濃度の溶液
を扱うことは、例えばアルコール法でペクチンを回収す
る場合のように、莫大な量のアルコールを必要として経
済的でなく、その他の方法によっても製造時の動力費用
や生産性の面から好ましくない。
Due to these circumstances, according to the conventional manufacturing method using pectin, the concentration limit of pectin is at most 1
%, and if it is higher than this, the efficiency will decrease due to the difficulty of separating undissolved residues. However, handling low-concentration solutions is not economical as it requires a huge amount of alcohol, as is the case when recovering pectin using the alcohol method, and other methods also reduce power costs and productivity during production. I don't like it from a certain point of view.

本発明の目的は、ペクチンの抽出濃度を上げることによ
り、効率よくペクチンを製造する方法を提供することで
あった。
An object of the present invention was to provide a method for efficiently producing pectin by increasing the extraction concentration of pectin.

本発明は、ペクチン含有植物よりペクチンを抽出して得
られる抽出液又はこの抽出液から分離された不溶解分に
、圧搾助剤を不溶解分100重量部に対し20重量部以
上添加し、圧搾して不溶解分を分離することを特徴とす
る、ペクチンの製造方法である。
In the present invention, a pressing aid is added to an extract obtained by extracting pectin from a pectin-containing plant or an insoluble component separated from this extract, and a pressing aid is added to the insoluble component in an amount of 20 parts by weight or more based on 100 parts by weight of the insoluble component. This is a method for producing pectin, which is characterized by separating insoluble matter.

本発明によれば、ペクチンの抽出液に圧搾助剤を添加し
混合することにより、不溶解分を硬質化して圧搾を容易
ならしめると共に、圧搾液の流路を確保し、スクリーン
の目詰まりを起こさずに効率よく液を回収することがで
きる。
According to the present invention, by adding and mixing a pressing aid to the pectin extract, insoluble matter is hardened to make pressing easier, and a flow path for the pressing liquid is secured, thereby preventing clogging of the screen. The liquid can be efficiently collected without causing any problems.

圧搾助剤としては珪藻土、パーライト、セルロース等の
r過助剤又はオガ屑、モミ殻、ペクチンの不溶解残有の
水洗物等を使用できるが、不溶解残有を硬質化するとい
う意味ではセルロース、オガ屑、モミ殻等が特に有効で
あり、スクリーンの目詰まり防止の意味からは珪藻土、
パーライト等のf過助剤が特に有効である。したがって
その実際の使用に当っては、その系に適合するようにこ
れらを適宜混合して使用する・ことも有利である。
As a pressing aid, it is possible to use diatomaceous earth, perlite, cellulose, or other additives such as sawdust, rice husks, and washed pectin with undissolved residue, but in the sense of hardening the undissolved residue, cellulose is used. , sawdust, rice husks, etc. are particularly effective, and diatomaceous earth,
F superaids such as perlite are particularly effective. Therefore, in actual use, it is advantageous to mix these as appropriate to suit the system.

圧搾助剤の添加量は、不溶解物の量すなわちペクチンの
濃度に比例して定めることが好ましく、該添加物の種類
やペクチン製造原料にもよるが、絶乾の不溶解分100
重量部に′対し一般に60〜200重量部が適当である
。添加量が多すぎる場合には液の回収率が低下して好ま
しくないし、逆に少なすぎる場合には十分な圧搾ができ
ない。該添加物の添加方法としては、普通は抽出に際し
て添加するが、抽出液に添加してもよバ、抽出液を遠心
分離等により分離した分離不溶分に該添加物を混合して
圧搾してもよい。圧搾装置としてはイ、ジブレス、ロー
ラーミル等の普通の装置が用いられる。
The amount of the pressing aid added is preferably determined in proportion to the amount of insoluble matter, that is, the concentration of pectin, and it depends on the type of the additive and the raw material for pectin production, but the amount of insoluble matter on bone dry 100
Generally, 60 to 200 parts by weight are suitable. If the amount added is too large, the recovery rate of the liquid will decrease, which is undesirable, while if it is too small, sufficient squeezing will not be possible. The additive is usually added during extraction, but it may also be added to the extract, or the additive may be mixed with the insoluble matter separated from the extract by centrifugation, etc., and then squeezed. Good too. As a pressing device, a common device such as a jig press, a roller mill, etc. is used.

実施例1 夏みかん搾汁果皮の乾燥物1.5 kgを水洗したのち
水中に添加し、全体量を20kgとしたのち塩酸でpH
を20とし、90℃で60分間攪拌して抽出を行った。
Example 1 1.5 kg of dried squeezed summer mandarin peel was washed with water, added to water to make a total amount of 20 kg, and then adjusted to pH with hydrochloric acid.
was set to 20, and the mixture was stirred at 90° C. for 60 minutes to perform extraction.

絶乾の不溶留分は約900gである。次いで抽出液に珪
藻土濾過助剤70g及びセルロース濾過助剤400gを
混合して圧搾し、不溶解残有3.3 kgと搾汁液17
.1kgを得た。搾汁液に珪藻土濾過助剤を0.5%添
加して清澄濾過を行い、得られたP液に60%濃度とな
るよフイソプロビルアルコールを加工、析出したペクチ
ンの沈殿を分離し、この沈殿を乾燥、粉砕して粉末ペク
チン220gを得た。製品ペクチンの原料果皮に対する
収率は147%であり、抽出液のペクチン濃度は140
%であった。
The absolute dry insoluble fraction is approximately 900 g. Next, 70 g of diatomaceous earth filter aid and 400 g of cellulose filter aid were mixed with the extract and squeezed to obtain 3.3 kg of undissolved residue and 17 g of squeezed liquid.
.. 1 kg was obtained. Add 0.5% diatomaceous earth filter aid to the squeezed juice and perform clarification filtration, process the resulting P liquid with fisoprobil alcohol to a concentration of 60%, separate the precipitated pectin, and remove the precipitate. was dried and ground to obtain 220 g of powdered pectin. The yield of product pectin based on the raw material peel is 147%, and the pectin concentration of the extract is 140%.
%Met.

実施例2 レモンの搾汁果皮の乾燥物1.5kl?を実施例1と同
様にして水洗、抽出し、絶乾の不溶留分850gの抽出
液にセルロース系濾過助剤500gを添加し、圧搾し、
て不溶残有2.61\9と搾汁液17、9 kgを得た
。以下実施例1と同様にして清澄濾過し、脱水、乾燥、
粉砕を行って粉末ペクチン275Iを得た。製品ペクチ
ンの原料果皮に対する収率は183%であり、抽出液の
ペクチン濃度は1.75%であった。
Example 2 1.5kl of dried lemon juice and peel? was washed with water and extracted in the same manner as in Example 1, and 500 g of cellulose filter aid was added to the bone-dry extract of 850 g of the insoluble fraction, and the mixture was squeezed.
2.61 kg of undissolved residue and 17.9 kg of squeezed liquid were obtained. Thereafter, clarifying filtration was carried out in the same manner as in Example 1, dehydration, drying,
Pulverization was performed to obtain powdered pectin 275I. The yield of product pectin based on the raw material pericarp was 183%, and the pectin concentration of the extract was 1.75%.

実施例6 夏みかん搾汁果皮の乾燥物21(gを実施例1と同様に
して水洗、抽出し、抽出液にセルロース濾過助剤200
I及びモミ殻800gを添加し、圧搾して不溶解残有3
.5 kgと搾汁液17.5kgを得た。以下実施例1
と同様にして清澄濾過し、脱水、乾燥、粉砕を行って粉
末ペクチン256gを得た。製品ペクチンの原料果皮に
対する収率は12.8%であり、ペクチン濃度は1.8
3%であった。
Example 6 21 (g) of dried fruit of squeezed summer mandarin peel was washed with water and extracted in the same manner as in Example 1, and 200 g of cellulose filter aid was added to the extract.
Add I and 800g of rice husks and press to remove undissolved residue 3
.. 5 kg and 17.5 kg of squeezed liquid were obtained. Example 1 below
Clarification filtration was carried out in the same manner as above, followed by dehydration, drying and pulverization to obtain 256 g of powdered pectin. The yield of product pectin based on the raw material peel is 12.8%, and the pectin concentration is 1.8
It was 3%.

比較例1 夏みたん搾汁果皮の乾燥物1 kgを実施例1と同様に
して水洗、抽出し、抽出液を圧搾助剤を加えずに遠心分
離して、残有4.6 kgと分離液154kgを得た。
Comparative Example 1 1 kg of dried fruit squeezed summer mitan fruit peel was washed with water and extracted in the same manner as in Example 1, and the extract was centrifuged without adding a pressing aid to separate the remaining 4.6 kg. 154 kg of liquid was obtained.

以下実施例1と同様にして清澄濾過し、脱水、乾燥、粉
砕を行って粉末ペクチン140gを得た。製品ペクチン
の原料果皮に対する収率は14.0%であり、抽出液の
濃度は0.96%であった。この場合は収率は良好であ
るが、抽出液が低濃度でペクチンの製造コストの点で好
ましくない。
Thereafter, clarification filtration, dehydration, drying, and pulverization were performed in the same manner as in Example 1 to obtain 140 g of powdered pectin. The yield of product pectin based on the raw material pericarp was 14.0%, and the concentration of the extract was 0.96%. In this case, the yield is good, but the concentration of the extract is low, which is unfavorable in terms of the production cost of pectin.

比較例2 レモンの搾汁果皮の乾燥物1.5 klilを実施例1
と同様にして水洗、抽出し、抽出液を圧搾助剤を加えず
に圧搾して、不溶解残有1.4 kgと搾汁液18.6
kgを得た。搾汁液中に不溶留分が多く、清nL濾過が
困難なため、さらに遠心分離を行って残有7.4 k1
7と分離液11.2 kgを得た。以下実施例1と同様
にして清澄濾過し、脱水、乾燥、粉砕を行って粉末ペク
チン201gを得た。製品ペクチンの原料果皮に対する
収率は13.4%であり、ペクチン濃度は実施例2のそ
れと同じである。実施例2と比°較して収率が著しく低
下する。
Comparative Example 2 1.5 kli of dried lemon juice and peel was added to Example 1.
Washed with water and extracted in the same manner as above, and the extract was pressed without adding any pressing aids to obtain 1.4 kg of undissolved residue and 18.6 kg of squeezed liquid.
I got kg. Since there was a large amount of insoluble fraction in the squeezed juice and it was difficult to filter the pure nL, further centrifugation was performed to reduce the remaining amount to 7.4 k1.
7 and 11.2 kg of separated liquid were obtained. Thereafter, clarification filtration, dehydration, drying, and pulverization were performed in the same manner as in Example 1 to obtain 201 g of powdered pectin. The yield of product pectin based on the raw material pericarp was 13.4%, and the pectin concentration was the same as that in Example 2. The yield is significantly lower than in Example 2.

比較例6 夏みかん搾汁果皮の乾燥物21(gを実施例1と同様に
して水洗、抽出し、絶乾の不溶留分1200Iの抽出液
にセルロース濾過助剤200g分が多く清澄濾過が困難
なため、さらに遠心分離を行って残有8.8 k!9と
分離液9.3 kgを得た。
Comparative Example 6 21 (g) of dried summer mandarin orange juice peel was washed with water and extracted in the same manner as in Example 1, and the bone-dried extract of insoluble distillate 1200I contained a large amount of cellulose filter aid 200g, making clarifying filtration difficult. Therefore, further centrifugation was performed to obtain 8.8 k!9 remaining and 9.3 kg of separated liquid.

以下実施例1と同様にして清澄濾過し、脱水、乾燥、粉
砕を行って粉末ペクチン165gを得た。製品ペクチン
の原料果fに対する収率は8゜3%であり、ペクチン濃
度は実施例6のそれと同じである。実施例6と比較して
収率が著しく低下する。
Thereafter, clarification filtration, dehydration, drying, and pulverization were performed in the same manner as in Example 1 to obtain 165 g of powdered pectin. The yield of product pectin based on raw fruit f was 8.3%, and the pectin concentration was the same as that in Example 6. The yield is significantly lower than in Example 6.

以上の実施例及び比較例から圧搾助剤の添加効果が明ら
かであり、好収率を維持しながらペクチン濃度を高める
ことが可能であることが知られる。
From the above Examples and Comparative Examples, the effect of adding the pressing aid is clear, and it is known that it is possible to increase the pectin concentration while maintaining a good yield.

なおこれらの実験で圧搾に用いた装置は、ハンスフエツ
ター社製スクリュープレス、P−スベンヤル型で、スク
リューの圧縮比1:8のものである。
The device used for compression in these experiments was a P-Svenjar type screw press manufactured by Hansfetter, with a screw compression ratio of 1:8.

出願人 三菱アセテート株式会社 代理人 弁理士 小 林 正 雄Applicant: Mitsubishi Acetate Co., Ltd. Agent: Patent Attorney Masao Kobayashi

Claims (1)

【特許請求の範囲】 1 ペクチン含有植物よりペクチンを抽出して得られる
抽出液又はこの抽出液から分離された不溶解分に、圧搾
助剤を不溶解分100重量部に対し20重量部以上添加
し、圧搾して不溶解分を分離することを特徴とする、ペ
クチンの製造方法。 2、圧搾助剤の添加量が不溶解分100重量部に対し3
0〜200重量部であることを特徴とする特許請求の範
囲第1項に記載の方法。
[Claims] 1. To the extract obtained by extracting pectin from a pectin-containing plant or to the insoluble matter separated from this extract, 20 parts by weight or more of a pressing aid is added per 100 parts by weight of the insoluble matter. A method for producing pectin, characterized by separating the insoluble matter by squeezing the pectin. 2. The amount of pressing aid added is 3 parts per 100 parts by weight of insoluble matter.
The method according to claim 1, characterized in that the amount is 0 to 200 parts by weight.
JP58238916A 1983-12-20 1983-12-20 Pectin manufacturing method Expired - Lifetime JPH0643445B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58238916A JPH0643445B2 (en) 1983-12-20 1983-12-20 Pectin manufacturing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58238916A JPH0643445B2 (en) 1983-12-20 1983-12-20 Pectin manufacturing method

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JPS60133002A true JPS60133002A (en) 1985-07-16
JPH0643445B2 JPH0643445B2 (en) 1994-06-08

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000043424A1 (en) * 1999-01-19 2000-07-27 Fuji Oil Co., Ltd. Pectin, process for producing the same, acidic protein foods with the use of the same and process for the production thereof
KR100370962B1 (en) * 2000-07-10 2003-02-06 지성규 Manufacturing meth od of Acetylated pectin for eliminating Endocrine Disrupter from the system

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000043424A1 (en) * 1999-01-19 2000-07-27 Fuji Oil Co., Ltd. Pectin, process for producing the same, acidic protein foods with the use of the same and process for the production thereof
US6632469B1 (en) 1999-01-19 2003-10-14 Fuji Oil Co., Ltd. Pectin, method for its production, acidic protein foods incorporating it and method for their production
KR100370962B1 (en) * 2000-07-10 2003-02-06 지성규 Manufacturing meth od of Acetylated pectin for eliminating Endocrine Disrupter from the system

Also Published As

Publication number Publication date
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