JPS5852999B2 - Stevioside Noseiseihou - Google Patents

Stevioside Noseiseihou

Info

Publication number
JPS5852999B2
JPS5852999B2 JP50054628A JP5462875A JPS5852999B2 JP S5852999 B2 JPS5852999 B2 JP S5852999B2 JP 50054628 A JP50054628 A JP 50054628A JP 5462875 A JP5462875 A JP 5462875A JP S5852999 B2 JPS5852999 B2 JP S5852999B2
Authority
JP
Japan
Prior art keywords
stevioside
exchange resin
water
extract
synthetic adsorbent
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
JP50054628A
Other languages
Japanese (ja)
Other versions
JPS51149300A (en
Inventor
亮一 伊勢
晃夫 小林
忠昭 葉賀
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.)
Sanyo Kokusaku Pulp Co Ltd
Original Assignee
Sanyo Kokusaku Pulp 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 Sanyo Kokusaku Pulp Co Ltd filed Critical Sanyo Kokusaku Pulp Co Ltd
Priority to JP50054628A priority Critical patent/JPS5852999B2/en
Publication of JPS51149300A publication Critical patent/JPS51149300A/en
Publication of JPS5852999B2 publication Critical patent/JPS5852999B2/en
Expired legal-status Critical Current

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  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)

Description

【発明の詳細な説明】 本発明はステビア原葉から水抽出したステビオサイド含
有水酸液をイオン交換樹脂によらずステビオサイドを選
択的に吸着する合成吸着剤により吸着させ、次いで有機
容媒を使用してステビオサイドを脱着させ、更に該有機
酸媒を弱塩基性陰イオン交換樹脂にて処理するステビオ
サイドの精製法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention involves adsorbing a stevioside-containing hydroxyl solution extracted with water from Stevia raw leaves using a synthetic adsorbent that selectively adsorbs stevioside without using an ion exchange resin, and then using an organic medium. The present invention relates to a method for purifying stevioside, in which stevioside is desorbed using stevioside, and the organic acid medium is further treated with a weakly basic anion exchange resin.

従来、ステビオサイドの精製法としてはステビア原葉を
水抽出したステビオサイド含有水抽出後を強酸性陽イオ
ン交換樹脂および弱塩基性陰イオン交換樹脂の両者を使
用する2段精製処理を行なってステビオサイドの純度を
45〜55%程度にまで高めた後、多量の水を濃縮する
か、あるいは乾固させ、次いでメタノール、ジオキサン
などの有機酵媒液として晶析させ、結晶を得る方法が広
く知られている。
Conventionally, the purification method for stevioside involves extracting Stevia leaves with water, which contains stevioside, and then performing a two-stage purification process using both a strongly acidic cation exchange resin and a weakly basic anion exchange resin to improve the purity of stevioside. A widely known method is to increase the amount of water to about 45-55%, then concentrate or dry up a large amount of water, and then crystallize as an organic enzyme solution such as methanol or dioxane to obtain crystals. .

しかしながら上述のイオン交換樹脂を用いる精製法はス
テプオサイドの損失が少なく、優れた方法であるが工業
化する場合には次に列記するような問題点が未だ解決さ
れていない。
However, although the purification method using the above-mentioned ion exchange resin is an excellent method with little loss of steposide, the following problems have not yet been solved in case of industrialization.

(1) 陽イオン交換樹脂にステビオサイド含有水抽
出液を通液する際に不躊物が生成し、陽イオン交換樹脂
を汚染し、通液性も不良にする。
(1) When a stevioside-containing aqueous extract is passed through a cation exchange resin, sludge is generated, contaminates the cation exchange resin, and impairs liquid permeability.

(2)陽イオン交換樹脂および陰イオン交換樹脂による
2段精製処理が必要であり、特に陰イオン交換樹脂の負
担が大きい。
(2) A two-stage purification process using a cation exchange resin and an anion exchange resin is required, which places a particularly heavy burden on the anion exchange resin.

(3)上記2段精製処理を行なうために処理後の液量が
著しく大量となる。
(3) Since the two-stage purification treatment is performed, the amount of liquid after treatment becomes extremely large.

(4)ステビオサイドを水藩液から晶析させる場合には
晶析率が低いので晶析率を向上させるためには水様を有
機溶媒系に転換させることが有効であり、この操作を行
なうに当り多量の水を濃縮して後に有機溶媒酸液とする
転換操作が必要である。
(4) When stevioside is crystallized from aqueous liquid, the crystallization rate is low, so in order to improve the crystallization rate, it is effective to convert the aqueous to an organic solvent system. It is necessary to condense a large amount of water and then convert it into an organic solvent acid solution.

従ってイオン交換法の利点を維持しながら上記未解決の
問題点を減少させる方法として、ステビア原葉を水抽出
する代わりに有機晦媒あるいは含水有機溶媒を用いて抽
出することが考えられる。
Therefore, as a method for reducing the above-mentioned unresolved problems while maintaining the advantages of the ion exchange method, it is conceivable to extract Stevia raw leaves using an organic eluent or a water-containing organic solvent instead of extracting them with water.

すなわち、溶媒抽出によって得られる抽出液をそのまま
直接にイオン交換処理することにより陽イオン交換樹脂
への通液時に発生する不醇物が抽出段階で除去されてい
るので不醇物を除去する操作を省略することができる。
In other words, by directly ion-exchanging the extract obtained by solvent extraction, the infusible substances generated when the liquid is passed through the cation exchange resin are removed during the extraction stage, so the operation to remove the insoluble substances is not necessary. Can be omitted.

また処理液が有機溶媒であるので蒸発熱が少なくて済む
から水抽出の場合よりも濃縮が容易となるなどの効果が
期待できるが、この場合にはイオン交換樹脂の精製効果
は水系よりも劣ること、および抽出工程で有機溶媒を大
量に用いるのでその有機晦媒回収が必要となり工程が水
抽出の場合よりも複雑となるなどの問題点が生じる。
In addition, since the processing liquid is an organic solvent, it requires less heat of evaporation, making it easier to concentrate than in the case of water extraction.However, in this case, the purification effect of the ion exchange resin is inferior to that of an aqueous system. In addition, since a large amount of organic solvent is used in the extraction process, it is necessary to recover the organic solvent, resulting in problems such as the process being more complicated than in the case of water extraction.

ステビオサイドの精製法としては、この池に活性炭を用
いる精製法も考えられるが、ステビオサイドは活性炭に
極めて強く吸着されるのでその脱着が困難であり、ステ
ビオサイドの回収率は低く、好ましい方法とは称し難い
As a purification method for stevioside, a purification method using activated carbon in this pond can be considered, but since stevioside is extremely strongly adsorbed to activated carbon, it is difficult to desorb it, and the recovery rate of stevioside is low, so this method cannot be called a preferable method. .

以上述べた如くステビオサイドの工業的精製法は未だ検
討を要する余地が犬であり、品質的にも価格的にも有利
な甘味剤としての地位を確立するためには効果的な精製
法を見出すことが強く要望されているのが現状である。
As mentioned above, there is still room for investigation into the industrial purification method of stevioside, and in order to establish its position as a sweetener that is advantageous in terms of quality and price, it is necessary to find an effective purification method. Currently, there is a strong demand for this.

従ってステビオサイドをよく吸着し、且つ脱着が容易で
あるような選択性の優れた池の吸着剤を鋭意研究探索し
た結果、合成吸着剤と称して市販されている製品が、こ
の目的に対して極めて有効であり、しかも後段の陰イオ
ン交換樹脂の負担を小さくすることを見出し本発明に到
達した。
Therefore, as a result of intensive research and search for a highly selective adsorbent that can adsorb stevioside well and desorb it easily, we found a commercially available product called a synthetic adsorbent that is extremely suitable for this purpose. The present invention was achieved by discovering that this method is effective and also reduces the burden on the anion exchange resin in the subsequent stage.

ここで言う合成吸着剤とは例えば三菱化成工業株式会社
より販売されているHP樹脂であり、スチレンとジビニ
ルベンゼンとを特殊な方法で重合させて製造した巨大網
状構造を有する硬くて不溶性である多孔性の非極性ポリ
マーであって、このものによる吸着は疎水結合、双極子
同志の相互作用および水素結合などによるVan de
r Waals力が重要な役割を果たすものであり、吸
着力も一般に小さいので、吸着物質を容易且つ定量的に
脱着することができる特徴を有している。
The synthetic adsorbent referred to here is, for example, HP resin sold by Mitsubishi Chemical Industries, Ltd., which is a hard, insoluble, porous resin with a giant network structure produced by polymerizing styrene and divinylbenzene using a special method. This is a non-polar polymer with a characteristic Van de adsorption due to hydrophobic bonds, interactions between dipoles, hydrogen bonds, etc.
The r Waals force plays an important role, and since the adsorption force is generally small, it has the characteristic that adsorbed substances can be easily and quantitatively desorbed.

本発明を以下に説明する。The invention will now be described.

すなわち、ステビア原葉の水抽出液と合成吸着剤とを水
懸濁液として気泡が入らないように充填したカラムに通
液することにより、水抽出液中のステビオサイドが、一
部の不純物と共に合成吸着剤に吸着される。
That is, by passing an aqueous extract of Stevia leaves and a synthetic adsorbent as an aqueous suspension through a column packed to prevent air bubbles from entering, stevioside in the aqueous extract is synthesized along with some impurities. Adsorbed by adsorbent.

この場合、合成吸着による抽出液の処理条件としては、
抽出液固形分1g当りの合成吸着剤使用量が5〜20r
IL11通液速度5V=1〜6の範囲が好ましい。
In this case, the conditions for processing the extract by synthetic adsorption are as follows:
The amount of synthetic adsorbent used per 1 g of extract solid content is 5 to 20 r.
IL11 liquid passing rate 5V is preferably in the range of 1 to 6.

通液時の水抽出液のpHは微酸性ないしは中性付近(p
H5から8)であることが必要である。
The pH of the aqueous extract during passage is slightly acidic or around neutral (p
H5 to H8) is required.

この時に合成吸着剤に吸着されなかった成分は水流出液
中に排出されるが、水流出液中にはステビオサイドの甘
味はほとんど感じられず、薄層クロマトグラフィー、高
速液体クロマトグラフィーなどの方法による分析結果か
らもステビオサイドの存在は認められなかったから水抽
出液中のステビオサイドは大略その全量が合成吸着剤に
吸着されて了っていることが判る。
At this time, the components that are not adsorbed by the synthetic adsorbent are discharged into the water effluent, but the sweetness of stevioside is hardly felt in the water effluent. Since the presence of stevioside was not recognized from the analysis results, it can be seen that almost all of the stevioside in the aqueous extract was adsorbed by the synthetic adsorbent.

ステビア原葉からステビオサイドを水で抽出するときは
、不純物の抽出をできるだけ押えるために中性付近で抽
出することが必要である。
When extracting stevioside from stevia leaves with water, it is necessary to extract at around neutrality in order to suppress the extraction of impurities as much as possible.

次いでこの抽出液を合成吸着剤のカラムに通じるときの
pHもステビオサイド吸着後の流出液の処理を含めて考
慮すると中性付近であることが好ましい。
Next, when this extract is passed through a synthetic adsorbent column, the pH is preferably around neutral considering the treatment of the effluent after stevioside adsorption.

すなわち、この流出液はいわば排水として不要のもので
あるが、腐敗しやすい有機物質を含むために環境保全上
、無処理で放流棄却することはできす、例えば生物処理
による分解、濃縮後、固形化または燃焼など何らかの処
理を行なうことが必要となる。
In other words, this effluent is unnecessary as wastewater, but since it contains perishable organic substances, it cannot be discharged and discarded without treatment for environmental conservation reasons.For example, after decomposition and concentration through biological treatment, solid It is necessary to carry out some kind of treatment such as oxidation or combustion.

特に濃縮を行なうときは濃縮操作および経費を軽減する
ために流出液量を可及的少量にすることが望ましい。
Particularly when concentrating, it is desirable to reduce the amount of effluent as much as possible in order to reduce concentration operations and costs.

そのために流出液を次回のステビア原葉の抽出に再度使
用することを行なうが、この場合抽出液のpHが5以下
のときはステビオサイドの抽出率が著しく低下するばか
りか、合成吸着剤カラムの通液性も不良となる。
For this purpose, the effluent is reused for the next extraction of Stevia leaves, but in this case, if the pH of the extract is below 5, not only will the extraction rate of stevioside drop significantly, but the synthetic adsorbent column will pass through. The liquid properties are also poor.

一般に流出液のpHは経済的にpHが降下しやすいので
、次回の抽出に用いるときは、pH7〜8に中和してか
ら使用することが望ましい。
Generally, the pH of the effluent tends to drop economically, so when it is used for the next extraction, it is desirable to neutralize it to pH 7-8 before use.

一方、流出液のpHが8以上のときは次回の抽出をアル
カリ性で行なうこととなり、不必要の不純物の抽出を徒
らに多くするので好ましくない。
On the other hand, if the pH of the effluent is 8 or higher, the next extraction will be carried out in an alkaline state, which is undesirable because unnecessary impurities will be unnecessarily extracted.

また、流出液を無処理で棄却することが許される場合で
も、少なくとも排水基準に定められたpHに中和しなけ
ればならない。
Furthermore, even if it is permissible to discard the effluent without treatment, it must be neutralized to at least the pH specified in the wastewater standards.

以上のような理由からステビア原葉の抽出および抽出液
の合成吸着剤への通液はpH5から8の範囲で行なうこ
とが必要である。
For the reasons mentioned above, it is necessary to perform the extraction of Stevia raw leaves and the passage of the extract through the synthetic adsorbent at a pH within the range of 5 to 8.

なお、抽出液をカラムへの通液性が良くないときは、抽
出液に適当量のp過助剤を混合分散して流過してから通
液すれば簡単に解決される。
Incidentally, if the permeability of the extract to the column is not good, this can be easily solved by mixing and dispersing an appropriate amount of p-superior into the extract and passing the liquid through the column.

水抽出液の通液を終えたら水洗することによってカラム
中に残存している非吸着成分を除去する。
After passing the aqueous extract, the column is washed with water to remove non-adsorbed components remaining in the column.

次いでメタノールあるいはジオキサンなどのステビオサ
イドを酵解することのできる有機溶媒を脱着溶媒に用い
てカラムに通液すると合成吸着剤に吸着されていた成分
はその大部分が容易に脱着し回収される。
Next, when an organic solvent capable of fermenting stevioside such as methanol or dioxane is used as a desorption solvent and the liquid is passed through the column, most of the components adsorbed on the synthetic adsorbent are easily desorbed and recovered.

ステビオサイドはこの吸着および脱着の過程を通じてほ
ぼ定量的に回収することができる。
Stevioside can be recovered almost quantitatively through this adsorption and desorption process.

有機溶媒により脱着回収処理を行なった合成吸着剤は若
干の吸着成分が残存しているが、希アルカリ水溶液によ
って再生が可能であり、反復使用することができる。
Although some adsorbed components remain in the synthetic adsorbent that has been subjected to desorption and recovery treatment using an organic solvent, it can be regenerated with a dilute aqueous alkaline solution and can be used repeatedly.

以上の処理を行なった場合の合成吸着剤へのステビオサ
イド水抽出物の吸着量、脱着溶媒によって脱着回収され
る固形分量および、この時のステビオサイド純度などは
水抽出物中のステビオサイド純度、処理した水抽出物と
合成吸着剤との割合、脱着に用いる有機溶媒の種類およ
び量などによって変動するが、一例を挙げると次の通り
である。
When the above treatment is performed, the amount of stevioside water extract adsorbed onto the synthetic adsorbent, the amount of solid content desorbed and recovered by the desorption solvent, and the stevioside purity at this time are determined by the stevioside purity in the water extract and the treated water. Although it varies depending on the ratio of extract and synthetic adsorbent, the type and amount of organic solvent used for desorption, etc., an example is as follows.

三菱化成工業株式会社製、合成吸着剤HP−i。Synthetic adsorbent HP-i manufactured by Mitsubishi Chemical Industries, Ltd.

の充填容積11に対して水抽出液固形分(ステビオサイ
ド純度16%)を150gおよび200g処理し、メタ
ノールで脱着回収した処、次の結果が得られた。
150 g and 200 g of water extract solid content (stevioside purity 16%) were treated with respect to a filling volume of 11, and desorbed and recovered with methanol, and the following results were obtained.

上表から明らかなようにステビオサイド純度16%の水
抽出物を合成吸着剤に吸着させた後、メタノールを脱着
溶媒とするとステビオサイドは90%以上の回収率で純
度40〜50%程度にまで精製することができることが
判る。
As is clear from the table above, when a water extract with a stevioside purity of 16% is adsorbed onto a synthetic adsorbent and methanol is used as the desorption solvent, stevioside is purified to a purity of about 40-50% with a recovery rate of 90% or more. It turns out that it is possible.

なお、ここではカラム法について説明したが、必ずしも
カラム法に限定するものではなく、バッチ法により本発
明法を実施することももちろん可能である。
Although the column method has been described here, it is not necessarily limited to the column method, and it is of course possible to carry out the method of the present invention by a batch method.

ステビオサイド含有水啼液を合成吸着剤処理したのみで
はステビオサイドの純度はまだ低くこのまま甘味料とし
て共する場合はもちろんのこと、晶析等の方法により精
製度の高いステビオサイドを得る場合においても製品収
率あるいは甘味料品質においても十分とはいえないので
更に陰イオン交換樹脂処理を行なう必要がある。
If the stevioside-containing water solution is only treated with a synthetic adsorbent, the purity of the stevioside is still low, not only when it is used as a sweetener, but also when obtaining highly purified stevioside by methods such as crystallization, the product yield is low. Also, since the quality of the sweetener is not sufficient, it is necessary to further treat it with an anion exchange resin.

この場合有機醇媒たとえばメタノールによって合成吸着
剤から脱着回収された溶液を濃縮乾固することなくその
まま弱塩基性陰イオン交換樹脂中に通液することができ
工程が簡略化され、しかもステビオサイドの損失はほと
んどない利点を有している。
In this case, the solution desorbed and recovered from the synthetic adsorbent using an organic adsorbent such as methanol can be directly passed through the weakly basic anion exchange resin without being concentrated to dryness, which simplifies the process and reduces the loss of stevioside. has few advantages.

このような処理を施すことによってステビオサイドの晶
析を更に容易ならしめ得ると共に、溶媒濃縮の熱量を軽
減させることができる。
By performing such a treatment, the crystallization of stevioside can be made easier, and the amount of heat required for concentrating the solvent can be reduced.

先にメタノールのような有機溶媒で陽イオン交換樹脂と
陰イオン交換樹脂との両者に通液する場合には水溶液通
液の場合と比較して精製効果が劣ると述べたが、本発明
法のように合成吸着剤処理を行ない、次いで陰イオン交
換樹脂処理を行なう時にはメタノール溶液でも陽、陰イ
オン交換樹脂法(水溶液通液)と同程度にまで精製する
ことが容易である。
It was previously stated that when an organic solvent such as methanol is passed through both a cation exchange resin and an anion exchange resin, the purification effect is inferior to that when an aqueous solution is passed, but the method of the present invention When a synthetic adsorbent treatment is performed and then an anion exchange resin treatment is performed, it is easy to purify even a methanol solution to the same level as the positive and anion exchange resin method (aqueous solution passage).

本発明の第一段の合成吸着剤によるステビオサイドの吸
着、脱着によって抽出溶媒たる水から晶析酵媒たる有機
溶媒への転換が容易に行ない得られ、その際水醇液の濃
縮が不要となる。
By adsorption and desorption of stevioside by the first stage synthetic adsorbent of the present invention, water, which is an extraction solvent, can be easily converted to an organic solvent, which is a crystallization fermentation medium, and there is no need to concentrate the aqueous solution. .

従ってステビア凍菜からステビオサイドの抽出を完全に
行なうために充分な量の水を使用することができる。
Therefore, a sufficient amount of water can be used to completely extract stevioside from stevia frozen vegetables.

その結果、メタノールを脱着溶媒とすればステビオサイ
ドを90%以上の回収率で純度40〜50%程度にまで
精製できることから今まで知られている公知の精製法と
比較して工程を著しく簡略化することが可能である。
As a result, if methanol is used as a desorption solvent, stevioside can be purified to a purity of about 40-50% with a recovery rate of 90% or more, which significantly simplifies the process compared to conventional purification methods. Is possible.

この後直ちに第二段の陰イオン交換樹脂処理を行なうこ
とにより第一段処理では除去しえなかった不純物をイオ
ン交換樹脂に吸着させ、一方ステビオサイドは全く吸着
させずに有機溶媒とともに流出させることにより不純物
を分離することができ収率および純度を高めることがで
きる。
Immediately after this, the second stage anion exchange resin treatment is carried out to adsorb impurities that could not be removed in the first stage treatment to the ion exchange resin, while stevioside is not adsorbed at all and flows out together with the organic solvent. Impurities can be separated to increase yield and purity.

この場合、処理すべき溶液中の固形分1g当りの陰イオ
ン交換樹脂の使用量は5〜20rfL11通液速度はs
v −i〜6の夫々の範囲が好ましい。
In this case, the amount of anion exchange resin used per 1 g of solid content in the solution to be treated is 5 to 20 rfL11 The flow rate is s
Each of the ranges from v-i to 6 is preferred.

なお、本発明法において合成吸着剤からの脱着晦媒およ
び陰イオン交換樹脂処理の廖媒にはメタノール、ジオキ
サンに限定するものではない。
In addition, in the method of the present invention, the desorption medium from the synthetic adsorbent and the transport medium for the anion exchange resin treatment are not limited to methanol and dioxane.

この方法の有利な点は有機躊媒の回収等はイオン交換樹
脂処理液のみに行なえばよく、一方不純物を含む水流出
液は一段目の合成吸着剤処理時のもののみでありイオン
交換樹脂の再生処理から生じる排水を含めても排水の液
量は大巾に軽減されることである。
The advantage of this method is that recovery of the organic solvent only needs to be carried out on the ion-exchange resin treated solution, while the water effluent containing impurities is only from the first-stage synthetic adsorbent treatment; Even including the wastewater generated from the recycling process, the amount of liquid wastewater is significantly reduced.

以上の結果から本発明法の有用性が明らかであるが、更
に比較例及び実施例を示して説明する。
Although the usefulness of the method of the present invention is clear from the above results, it will be further explained by showing comparative examples and examples.

比較例 ステビア凍菜を熱水抽出した抽出液1500cc(pH
5,7、固形分78g1純度15.4%、ステビオサイ
ド12.0g)を強酸性陽イオン交換樹脂(商品名、ア
ンバーライトIR−120H型)11を充填したカラム
および弱塩基性陰イオン交換樹脂(オルガノ服装アンバ
ーライトIRA−930H型)11を充填したカラムに
Sv約3で順次通液した処、IR−12Q力ラム通液時
に析出不溶物を生じ、通液性が不良となる現象が認めら
れた〇 二段処理後の総液量は2500cc(水酸液)に増大し
、固形分22.8g(純度50.0%、ステビオサイド
11.4g)を得た。
Comparative Example 1500 cc of hot water extract of Stevia frozen vegetables (pH
5,7, solid content 78g 1 purity 15.4%, stevioside 12.0g) was packed in a column filled with a strongly acidic cation exchange resin (trade name, Amberlite IR-120H type) 11 and a weakly basic anion exchange resin ( When the liquid was sequentially passed through a column filled with Organo Clothing Amberlite IRA-930H type 11 at Sv of approximately 3, a phenomenon was observed in which insoluble matter was precipitated when the liquid was passed through the IR-12Q column, resulting in poor liquid permeability. After the two-stage treatment, the total liquid volume increased to 2500 cc (hydroxide solution), and a solid content of 22.8 g (purity 50.0%, stevioside 11.4 g) was obtained.

この段階でのステビオサイドの回収率は95.0%であ
った。
The recovery rate of stevioside at this stage was 95.0%.

2500CCの水酸液を濃縮乾固した後、メタノール1
00CCに再酵解し、不晦物を除去して5℃で48時間
晶析させた。
After concentrating 2500 CC of hydroxyl solution to dryness, methanol 1
The mixture was fermented again to 00CC, impurities were removed, and crystallized at 5°C for 48 hours.

その結果は結晶8.0g(純度85.5%、ステビオサ
イド6.84g)および晶析残渣13.6g(純度29
.8%、ステビオサイド4.06g)を得た。
The results were 8.0 g of crystals (purity 85.5%, 6.84 g stevioside) and 13.6 g crystallization residue (purity 29%).
.. 8% stevioside (4.06 g) was obtained.

実施例 比較例と同一の抽出液1500cc(固形分78g1純
度15.4%、ステビオサイド12.0g)を三菱化成
■製合成吸着剤)JP−101#を充填したカラムにS
■約5で通液し、非吸着成分を水洗により除去した。
S
(2) The solution was passed through the solution at a temperature of about 5, and non-adsorbed components were removed by washing with water.

この通液時に不溶物の析出は認められず、通液性は良好
であった。
During this liquid passage, no precipitation of insoluble matter was observed, and the liquid permeability was good.

続いて吸着成分を回収するためメタノール11で脱着し
たが、始めに流出する液はメタノール含有量が少な、く
、水含有量が多いのでこの部分を除去し、メタノール含
有量が高くなってから液を回収した。
Next, in order to recover the adsorbed components, desorption was performed using methanol 11, but since the first liquid that flows out has a low methanol content and a high water content, this part was removed, and the liquid was removed after the methanol content became high. was recovered.

このメタノール溶液をメタノールで飽和させた弱塩基性
陰イオン交換樹脂(商品名、アンバーライト■RA−9
30H型)17を充填したカラムにSVVS2通液した
This methanol solution is saturated with methanol to create a weakly basic anion exchange resin (trade name: Amberlite RA-9).
SVVS2 was passed through a column packed with 30H type) 17.

二段処理後の総液量は1500cc(メタノール酸液)
であり、固形分21.og(純度53.3%、ステビオ
サイド11.2g)を得た。
Total liquid volume after two-stage treatment is 1500cc (methanol acid liquid)
and the solid content is 21. og (purity 53.3%, stevioside 11.2 g) was obtained.

この段階でのステビオサイドの回収率は93.2%であ
った。
The recovery rate of stevioside at this stage was 93.2%.

1500ccのメタノール溶液を100ccにまで濃縮
した後、不溶物を除去し、5℃で48時間晶析させた。
After concentrating 1500 cc of methanol solution to 100 cc, insoluble materials were removed and crystallization was performed at 5° C. for 48 hours.

その結果、結晶8.0g(純度87.9%、ステビオサ
イド7.03g)および晶析残渣12.5g(純度29
.6%、ステビオサイド3.7g)を得た。
As a result, 8.0 g of crystals (purity 87.9%, 7.03 g of stevioside) and 12.5 g of crystallization residue (purity 29%) were obtained.
.. 6% stevioside (3.7 g) was obtained.

Claims (1)

【特許請求の範囲】[Claims] 1 ステビア・レバウディアナ・ベルトニーの乾燥葉を
pH5,O〜8.0で水若しくは熱水と接触させて得ら
れる抽出液を、p)15.0〜8.0で非極性合成吸着
剤と接触させてステビオサイドを選択的に該吸着剤に吸
着させた後、該吸着剤を有機醇媒と接触させてステビオ
サイドを脱着させ、更に該ステビオサイド含水有機溶媒
を弱塩基性陰イオン交換樹脂と接触させる一連の工程結
合を特徴とするステビオサイドの精製法。
1. The extract obtained by contacting the dried leaves of Stevia rebaudiana Bertoni with water or hot water at pH 5,0 to 8.0 is brought into contact with a non-polar synthetic adsorbent at p) 15.0 to 8.0. After selectively adsorbing stevioside onto the adsorbent, the adsorbent is contacted with an organic solvent to desorb stevioside, and the stevioside-containing organic solvent is further contacted with a weakly basic anion exchange resin. Stevioside purification method characterized by process coupling.
JP50054628A 1975-05-12 1975-05-12 Stevioside Noseiseihou Expired JPS5852999B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP50054628A JPS5852999B2 (en) 1975-05-12 1975-05-12 Stevioside Noseiseihou

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP50054628A JPS5852999B2 (en) 1975-05-12 1975-05-12 Stevioside Noseiseihou

Publications (2)

Publication Number Publication Date
JPS51149300A JPS51149300A (en) 1976-12-22
JPS5852999B2 true JPS5852999B2 (en) 1983-11-26

Family

ID=12976007

Family Applications (1)

Application Number Title Priority Date Filing Date
JP50054628A Expired JPS5852999B2 (en) 1975-05-12 1975-05-12 Stevioside Noseiseihou

Country Status (1)

Country Link
JP (1) JPS5852999B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2020536124A (en) * 2017-09-28 2020-12-10 ピュアサークル ユーエスエー インコーポレイテッド How to prepare steviol glycosides and their use
US11773125B2 (en) 2010-03-12 2023-10-03 Purecircle Usa Inc. Methods of preparing steviol glycosides and uses of the same

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5951258B2 (en) * 1976-04-07 1984-12-13 守田化学工業株式会社 sweetener
JPS5430199A (en) * 1977-08-08 1979-03-06 Sanyo Kokusaku Pulp Co Ltd Purification of stevia sweetening agnet
JPS5441898A (en) * 1977-09-06 1979-04-03 Mitsubishi Chem Ind Ltd Purification of stevioside
JPS5441899A (en) * 1977-09-06 1979-04-03 Mitsubishi Chem Ind Ltd Purification of stevioside
JPS5478388A (en) * 1977-12-05 1979-06-22 Mitsubishi Chem Ind Ltd Regenerating method for synthetic adsorbing resin
JPS54132218A (en) * 1978-04-01 1979-10-15 Toyo Soda Mfg Co Ltd Separation of saponin constituents
JPS54132599A (en) * 1978-04-04 1979-10-15 Sanyo Kokusaku Pulp Co Ltd Separation and purification of stevioside sweetening
EP0302948B1 (en) * 1987-07-21 1993-12-01 Roger H. Giovanetto Process for obtaining steviosides from plants

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5191300A (en) * 1975-02-10 1976-08-10 Sutebiosaido no seiseihoho

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5191300A (en) * 1975-02-10 1976-08-10 Sutebiosaido no seiseihoho

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11773125B2 (en) 2010-03-12 2023-10-03 Purecircle Usa Inc. Methods of preparing steviol glycosides and uses of the same
JP2020536124A (en) * 2017-09-28 2020-12-10 ピュアサークル ユーエスエー インコーポレイテッド How to prepare steviol glycosides and their use

Also Published As

Publication number Publication date
JPS51149300A (en) 1976-12-22

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