JPH09308455A - Production of condensed extract of dried fish meat - Google Patents

Production of condensed extract of dried fish meat

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Publication number
JPH09308455A
JPH09308455A JP8127998A JP12799896A JPH09308455A JP H09308455 A JPH09308455 A JP H09308455A JP 8127998 A JP8127998 A JP 8127998A JP 12799896 A JP12799896 A JP 12799896A JP H09308455 A JPH09308455 A JP H09308455A
Authority
JP
Japan
Prior art keywords
liquid
extract
concentrated
mixture
gas
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
JP8127998A
Other languages
Japanese (ja)
Other versions
JP3568688B2 (en
Inventor
Yukihiko Imaizumi
幸彦 今泉
Takeshi Ayukawa
毅 鮎川
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.)
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry Co Ltd
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Filing date
Publication date
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Priority to JP12799896A priority Critical patent/JP3568688B2/en
Publication of JPH09308455A publication Critical patent/JPH09308455A/en
Application granted granted Critical
Publication of JP3568688B2 publication Critical patent/JP3568688B2/en
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Expired - Lifetime legal-status Critical Current

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  • Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain a condensed extract of dried fish meat, improved in flavor, taste, especially fishy smell, foreign taste, etc., by extracting vaporizable components from a mixture of a dried fish meat and water in a separation liquid by a gas-liquid counter current contacting apparatus, condensing the remaining extract and mixing the resultant condensate with the separation liquid. SOLUTION: At first, 50% or more of vaporizable components are extracted from a mixture of a dried fish body and water or an extracted essence of the mixture as a separation liquid by a gas-liquid counter current contacting apparatus. Subsequently, the remaining liquid of the removal of the vaporizable components is condensed after removing solid components of the dried fish meat in the case of using the mixture in the above process, or as it is in the case of using the extracted essence of the mixture. Finally, the obtained condensate is mixed with the separation liquid. Regarding a condensation method, preferably the liquid is condensed under reduced pressure at a condensation rate of two or more times, and the separation liquid is mixed with the condensate after it is held for 5-40min at 65-85 deg.C. As the gas-liquid counter current contact apparatus, a rotary circular-cone tower having an internal structure composed of alternate combinations of a rotary circular cone and a fixed circular cone, in which the liquid to be treated flows down from the upper part in a thin film state and at the same time gas ascends from the bottom, is preferably.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は、節類と水の混合物
またはその抽出エキスから、気液向流接触装置により揮
発性成分を一旦抽出、凝縮して分離液として回収し、一
方、揮発性成分を抽出された後の抽出エキスに対して、
濃縮、あるいは、濃縮および加熱等の処理を実施し、そ
の後に、前記揮発性成分の分離液を混合する、香気、風
味、特に生臭み、雑味、不快臭の改善された節類の濃縮
エキスを製造する方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method in which a volatile component is once extracted and condensed from a mixture of knots and water or an extract thereof by a gas-liquid countercurrent contact device and recovered as a separated liquid. For the extracted extract after the components have been extracted,
Concentrated extract of knots with improved aroma, flavor, especially fishy odor, unpleasant odor, which is subjected to treatment such as concentration or concentration and heating, and then mixing the separated liquid of the volatile components. To a method of manufacturing.

【0002】[0002]

【従来の技術】従来、節類の濃縮エキスの製造は、節類
特有の香気成分の揮発性が高いことにより、香気の低下
を防止するために、節類を高濃度にして抽出し、濃縮倍
率を抑える方法、逆浸透膜を用いて濃縮する方法、ある
いは、減圧濃縮時に発生する凝縮液の極一部をカットバ
ックする方法等で行われている。しかしながら、高濃度
で抽出する方法では、水添加量が少ないため、収率が悪
く、また、抽出成分のバランスが不安定で風味、香気質
が安定せず、雑味、不快臭が強い。逆浸透法では、濃縮
度が低く、生臭みが強い。カットバックする方法では、
香気のバランスが大きく変わる。さらには、各方法と
も、濃縮後の殺菌、除菌処理で風味、香気の劣化が起こ
るという問題を抱えている。
2. Description of the Related Art Conventionally, a concentrated extract of knots has been produced by concentrating the knots in a high concentration in order to prevent a decrease in aroma due to the high volatility of the aroma components peculiar to knots. It is carried out by a method of suppressing the magnification, a method of concentrating using a reverse osmosis membrane, or a method of cutting back a very small part of the condensate generated at the time of concentration under reduced pressure. However, in the method of extracting at a high concentration, since the amount of water added is small, the yield is poor, and the balance of the extracted components is unstable, the flavor and aroma are not stable, and the taste and unpleasant odor are strong. The reverse osmosis method has a low degree of concentration and a strong fishy odor. The way to cut back is
The balance of aroma changes greatly. Furthermore, each method has a problem that flavor and aroma are deteriorated by sterilization and sterilization treatment after concentration.

【0003】[0003]

【発明が解決しようとする課題】前項記載の従来技術の
背景下に、本発明は、香気、風味の改善された節類の濃
縮エキスを提供することを目的とする。
DISCLOSURE OF THE INVENTION Under the background of the prior art described in the preceding paragraph, the present invention aims to provide a concentrated extract of knotweed with improved aroma and flavor.

【0004】[0004]

【課題を解決するための手段】本発明者は、前記課題を
解決するため鋭意検討した結果、気液向流接触装置を用
いて、特定条件範囲であらかじめ揮発性成分を分離して
おき、かつ、分離後の抽出エキスも特定条件範囲で濃縮
等の処理をし、最後に、濃縮液と前記分離した揮発性成
分を混合することにより、香気、風味、特に生臭み、雑
味、不快臭が改善されることを見出し、本発明をなすに
至った。
Means for Solving the Problems As a result of intensive studies for solving the above problems, the present inventor has previously separated volatile components within a specific condition range by using a gas-liquid countercurrent contact device, and The extracted extract after separation is also subjected to treatment such as concentration under a specific condition range, and finally, by mixing the concentrated liquid with the separated volatile component, aroma, flavor, particularly fishy odor, unpleasant taste, and unpleasant odor are generated. The inventors have found that it is improved and have completed the present invention.

【0005】即ち本発明は、節類と水の混合物、または
これの抽出エキスから揮発性成分の50%以上を気液向
流接触装置によって分離液として抽出した後、前記混合
物をそのまま使用した場合は節類の固形分を取り除き、
抽出エキスを使用した場合はそのまま残存した液を濃縮
し、該濃縮液に前記揮発性成分の分離液を混合すること
を特徴とする節類濃縮エキスの製造方法である。
That is, according to the present invention, when 50% or more of volatile components are extracted as a separated liquid from a mixture of knots and water, or an extract thereof by using a gas-liquid countercurrent contact device, the mixture is used as it is. Removes the solid content of knots,
When an extract is used, the method is a method for producing a concentrated extract of node, which comprises concentrating the remaining liquid and mixing the concentrated liquid with the separated liquid of the volatile components.

【0006】次に、本発明について、さらに詳細に説明
する。本発明で使用する節類とは、鰹節、鯖節、煮干
し、宗田節等をいい、その形状としては、抽出に適した
粉末、荒節、薄片状のものが好ましい。揮発性成分の抽
出にあたって、節類と水の混合物を不溶性固形分を分離
しないまま利用する場合は流動性を有する液性の状態が
好ましく、粉末状の節類の使用が好ましい。香気質の点
から言えば、凍結粉砕品が適している。粒の粗い節類を
使用する場合は、水を添加した後、ビーズミル、マスコ
ロイダー、タッピングミル等の摩砕機で、あらかじめ微
粒化またはスラリー化してから気液向流接触装置の処理
に供するとよい。
Next, the present invention will be described in more detail. The knots used in the present invention include bonito knots, mackerel knots, dried sardines, soda knots, etc., and the shape thereof is preferably powder, rough knots or flakes suitable for extraction. When a mixture of knots and water is used without separating insoluble solids in the extraction of volatile components, a liquid state having fluidity is preferable, and powdery knots are preferably used. From the point of view of aroma quality, freeze-ground products are suitable. When using coarse-grained knots, it is advisable to add water and then use a mill such as a bead mill, a mass colloider, or a tapping mill to atomize or slurry them in advance and then subject them to treatment with a gas-liquid countercurrent contact device. .

【0007】節類に加えられる水の量は、風味、香気成
分を充分に抽出しうる範囲でできるだけ少量が好まし
く、節類の重量に対して、3〜20倍量程度が適してい
る。水が加えられた節類の不溶性固形分を分離し、予備
的にエキスの抽出をするとよい。このエキス抽出条件は
特に限定されず、望まれる品質を発現するよう設定すれ
ばよく、通常は100℃以下で実施すればよい。加熱感
を抑え、フレッシュ感を強調したいときは、50℃以下
で処理することが望ましい。抽出溶媒は、通常水でよい
が、場合によっては、一部エタノール等のアルコールを
混和してもよい。
The amount of water added to the knots is preferably as small as possible within the range where the flavor and aroma components can be sufficiently extracted, and about 3 to 20 times the amount of the knots is suitable. It is advisable to separate the insoluble solid content of the knots to which water has been added and extract the extract in advance. The conditions for extracting the extract are not particularly limited and may be set so as to express the desired quality, and it is usually carried out at 100 ° C or lower. In order to suppress the feeling of heating and emphasize the feeling of freshness, it is desirable to perform the treatment at 50 ° C. or lower. The extraction solvent is usually water, but in some cases, alcohol such as ethanol may be partially mixed.

【0008】節類と水の混合物、またはこの混合物の抽
出エキスに対して、香気質の主因物質である揮発性成分
を濃縮前にあらかじめ抽出・分離する。抽出・分離に当
たっては、蒸留法、精留法、吸着剤による吸着脱離法等
がよく知られているが、これらは、香気成分のバランス
が大きく変わってしまうこと、および、揮発性成分を高
濃度に濃縮しにくい等の欠点があり、本発明において
は、気液向流接触装置を用いて抽出、凝縮することによ
り、揮発性成分を分離・回収する。特に、回転円錐と固
定円錐が交互に組み合わされ、被処理液が上部から薄膜
状に流下し、下部から抽出媒体の気体が上昇する内部構
造となっている回転円錐塔型の気液向流装置が、効率、
操作性の点で優れている。本装置の実例としては、特公
平7−22646号公報に示されているような装置が挙
げられる。すなわち、節類と水の混合物、または、それ
の抽出物と抽出媒体としての水蒸気を向流接触させ、揮
発性成分を水蒸気で抽出し、その後、冷却器で凝縮させ
てから揮発性成分を回収する。節類原料の香気成分のロ
スを少なくするという観点から見ると、節類と水の混合
物を、固形物を分離せずに気液向流接触装置に供する方
法の方が優れている。揮発性成分の抽出にあたっては、
温度条件は特に限定されず、香気質の劣化のない範囲で
実施すればよい。通常は、品温100℃以下で実施す
る。また、加熱感を抑えフレッシュ感を強調したいとき
は、50℃以下で処理することが望ましい。揮発性成分
の抽出率は、原料中にある揮発性成分の50%以上を抽
出・回収する。50%未満の場合は、詳細な理由は不明
であるが香気質の改善効果がほとんどみられず、本発明
の目的に適さない。好ましくは70%、より好ましくは
80%である。抽出率は、分離・回収された液と原料の
節類と水の混合物、またはこれの抽出エキスを、希釈液
を数段階作製し、官能的に強度を比較すれば、容易に判
定することできる。揮発性成分を抽出・回収するに際し
ては、できるだけ高濃度に回収することが好ましく、回
収した分離液量は原料の30%以下、より好ましくは2
0%以下が本発明に適しており、揮発性成分の抽出の操
作条件の調整、設定により実施する。
A volatile component, which is a main factor of aroma, is extracted and separated from a mixture of knots and water, or an extract of the mixture, before concentration. Distillation, rectification, and adsorption / desorption with an adsorbent are well known for extraction and separation.However, these greatly change the balance of aroma components and increase volatile components. There are drawbacks such as difficulty in concentration, and in the present invention, volatile components are separated and recovered by extraction and condensation using a gas-liquid countercurrent contact device. In particular, a rotating cone tower type gas-liquid countercurrent device having an internal structure in which rotating cones and fixed cones are alternately combined, the liquid to be treated flows down from the upper part in a thin film shape, and the gas of the extraction medium rises from the lower part. But efficiency,
Excellent in operability. An example of this device is a device as disclosed in Japanese Examined Patent Publication No. 7-22646. That is, a mixture of knots and water, or an extract thereof and steam as an extraction medium are brought into countercurrent contact to extract volatile components with steam, and then the volatile components are condensed in a cooler before recovering the volatile components. To do. From the viewpoint of reducing the loss of the aroma component of the knots raw material, the method of supplying the knots and water mixture to the gas-liquid countercurrent contact device without separating the solids is superior. When extracting volatile components,
The temperature condition is not particularly limited, and it may be carried out within a range where the aroma is not deteriorated. Usually, it is carried out at a product temperature of 100 ° C or lower. Further, in order to suppress the feeling of heating and emphasize the feeling of freshness, it is desirable to perform the treatment at 50 ° C. or lower. The extraction rate of volatile components is such that 50% or more of the volatile components in the raw material are extracted and recovered. If it is less than 50%, the detailed reason is not clear, but the effect of improving the aroma quality is hardly seen, and it is not suitable for the purpose of the present invention. It is preferably 70%, more preferably 80%. The extraction rate can be easily determined by preparing a mixture of the separated and recovered liquid, the raw material knots and water, or an extract of this, in several dilution solutions and comparing the strengths organoleptically. . When extracting and recovering volatile components, it is preferable to recover as high a concentration as possible, and the recovered amount of separated liquid is 30% or less of the raw material, more preferably 2%.
0% or less is suitable for the present invention, and is carried out by adjusting and setting operating conditions for extraction of volatile components.

【0009】揮発性成分の抽出・分離後、残存した節類
と水の混合物、あるいはその抽出エキスを濃縮する。節
類と水の混合物の場合は、節類の固形物をあらかじめ分
離してから濃縮工程に供する。本発明における濃縮は、
減圧濃縮法、逆浸透法で実施する。それぞれ条件は、通
常採用されている範囲から設定すればよい。また、濃縮
倍率は、最終的な濃縮エキスの目標濃度を基準に、揮発
性成分の分離液の混合戻し量を勘案して設定すればよ
い。
After the extraction and separation of the volatile components, the remaining mixture of knots and water or the extract thereof is concentrated. In the case of a mixture of knots and water, the knots solids are separated in advance and then subjected to the concentration step. The concentration in the present invention is
It is carried out by a vacuum concentration method or a reverse osmosis method. Each condition may be set within a range that is normally adopted. Further, the concentration ratio may be set in consideration of the mixing back amount of the separated liquid of the volatile components, based on the final target concentration of the concentrated extract.

【0010】濃縮後、必要に応じて殺菌、除菌処理を実
施し、濃縮前に取得していた揮発性成分の分離液を混合
する。殺菌、除菌は、プレート式、タンク内バッチ式等
の通常の加熱殺菌、精密濾過膜を使用した膜濾過による
除菌の方法等を適用すればよい。分離液の混合戻し量
は、通常全量戻すが、最終エキスの濃度および香気質の
調整のために、一部分だけにしてもよい。また、逆に、
濃縮液を減じて混合してもよく、その際には、香気質が
より強調された濃縮エキスとなる。
After concentration, sterilization and sterilization treatment are carried out if necessary, and the separated liquid of volatile components obtained before concentration is mixed. For the sterilization and sterilization, it is possible to apply a normal heat sterilization such as a plate type or a batch type in a tank, or a sterilization method by membrane filtration using a microfiltration membrane. The amount of the separated liquid to be mixed back is usually returned to the total amount, but it may be only a part for adjusting the concentration and aroma of the final extract. On the contrary,
The concentrated liquid may be reduced and mixed, in which case a concentrated extract in which the aroma is further emphasized.

【0011】さらに、濃縮を減圧濃縮で実施する際に、
3倍以上濃縮すると、最終の濃縮エキスの生臭み、不快
臭が特に低下する。また、2倍以上濃縮し、その後、6
5〜85℃の範囲で5〜40分間加熱保持すると、最終
の濃縮エキスの生臭み、雑味が特に低下し、また、加熱
感のある好ましい香気が強化される。逆浸透法で濃縮し
た場合、濃縮後の殺菌、除菌処理を精密膜濾過法で実施
すると、最終の濃縮エキスの加熱感、えぐ味が特に低下
し、軽い好ましい香気が強化される。また、抽出工程か
ら50℃以下で処理すると、加熱感が弱く、それにも拘
わらず生臭み、不快臭の低下したタイプの濃縮エキスが
得られる。
Further, when the concentration is carried out under reduced pressure,
If the extract is concentrated 3 times or more, the final concentrated extract has a particularly reduced unpleasant smell and unpleasant odor. Concentrate more than 2 times, then 6
When the mixture is heated and held in the range of 5 to 85 ° C. for 5 to 40 minutes, the final concentrated extract has a particularly reduced fishy odor and miscellaneous taste, and the preferable aroma with a feeling of heating is enhanced. In the case of concentrating by the reverse osmosis method, when the sterilization and sterilization treatment after the concentration are carried out by the fine membrane filtration method, the feeling of heating and the astringent taste of the final concentrated extract are particularly lowered, and the light and preferable aroma is enhanced. Further, if the treatment is carried out at 50 ° C. or lower from the extraction step, a concentrated extract of the type having a weak heating sensation and nevertheless having a reduced fishy odor and unpleasant odor can be obtained.

【0012】[0012]

【発明の実施の形態】以下、実施例および比較例を示し
本発明を具体的に説明するが、本発明はこれらにより何
ら限定されるものではない。
BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be specifically described below by showing Examples and Comparative Examples, but the present invention is not limited to these.

【0013】[0013]

【実施例1および比較例1、2】カツオ節の荒節粉(粒
径約2mm)10重量部に、水90重量部加え、スーパ
ーマスコロイダーにて摩砕し、粒径約100μmのスラ
リーとし、60℃まで昇温し、1時間加熱した。その
後、気液向流接触装置に供し、揮発性成分を抽出した。
気液向流接触装置の運転条件としては、スラリー品温7
0℃、揮発性成分の凝縮液量(分離液量)3%(対スラ
リー比)で、揮発性成分の抽出率は50%であった。次
に、処理後のスラリーを濾布濾過およびセライト濾過に
より、カツオ節粉等の不溶固形物を除去して清澄化し、
50℃にて減圧濃縮を実施した。処理液を2倍濃縮し、
得られた濃縮液に前記の揮発性成分の分離液を全量混合
し、カツオ節濃縮エキスを得た。
[Example 1 and Comparative Examples 1 and 2] 90 parts by weight of water was added to 10 parts by weight of bonito flakes powder (particle size: about 2 mm), and the mixture was ground with a supermass colloider to obtain a slurry having a particle size of about 100 μm. It heated up to 60 degreeC and heated for 1 hour. Then, the mixture was subjected to a gas-liquid countercurrent contact device to extract volatile components.
The operating conditions of the gas-liquid countercurrent contact device are slurry temperature 7
At 0 ° C., the volatile component condensate amount (separated liquid amount) was 3% (vs. the slurry ratio), and the volatile component extraction rate was 50%. Next, the treated slurry is clarified by removing insoluble solid matter such as bonito flakes by filter cloth filtration and Celite filtration,
Concentration under reduced pressure was carried out at 50 ° C. Concentrate the treatment solution twice,
The concentrated liquid thus obtained was mixed with all the separated liquid of the volatile components to obtain a concentrated extract of dried bonito flakes.

【0014】比較例1として、気液向流接触装置による
処理をしない以外は、実施例1と同一の条件で実施して
比較品としてのカツオ節濃縮エキスを得た。また、比較
例2として、揮発性成分の抽出率が45%である以外
は、実施例1と同一の条件で実施して比較品としてのカ
ツオ節濃縮エキスを得た。実施例1、比較例1、2で得
られたカツオ節濃縮エキスを60℃の温湯でBRIX
0.5%になるようにそれぞれ希釈し、希釈液を専門パ
ネラー16名により品質の比較評価を実施した。その結
果を表1に示す。これらの結果により、実施例1が品質
的に優位であることが判明した。
Comparative Example 1 was carried out under the same conditions as in Example 1 except that the treatment with a gas-liquid countercurrent contact device was omitted to obtain a bonito-fruit concentrated extract as a comparative product. Further, as Comparative Example 2, a bonito-fruit-concentrated extract as a comparative product was obtained by performing the same conditions as in Example 1 except that the extraction rate of volatile components was 45%. The bonito flakes concentrated extracts obtained in Example 1 and Comparative Examples 1 and 2 were treated with BRIX in hot water at 60 ° C.
Each was diluted to 0.5% and the diluted solution was subjected to comparative evaluation of quality by 16 professional panelists. Table 1 shows the results. From these results, it was found that Example 1 was superior in quality.

【0015】[0015]

【表1】 [Table 1]

【0016】[0016]

【実施例2、3および比較例3】カツオ節の荒節粉(粒
径約3mm)10重量部に、水50重量部加え、80℃
まで昇温し、30分間加熱し、その後、濾布濾過、セラ
イト濾過により、カツオ節粉等の不溶固形物を除去し
て、清澄化した抽出エキスを得た。引き続き、気液向流
接触装置により揮発性成分を抽出した。気液向流接触装
置の運転条件としては、スラリー品温80℃、揮発性成
分の凝縮液量(分離液量)5%(対抽出エキス液量比)
で、揮発性成分の抽出率は50%であった。次に、気液
向流装置処理後の抽出エキスを40℃にて減圧濃縮を実
施した。3倍まで濃縮し、得られた濃縮液に前記の揮発
性成分の分離液を全量混合し、カツオ節濃縮エキスを得
た。
[Examples 2 and 3 and Comparative Example 3] 50 parts by weight of water was added to 10 parts by weight of coarse bonito powder (particle diameter of about 3 mm) at 80 ° C.
The mixture was heated up to 30 minutes, heated for 30 minutes, and then filtered to remove insoluble solids such as dried skipjack powder and filtered to obtain a clarified extract. Subsequently, volatile components were extracted by a gas-liquid countercurrent contact device. The operating conditions of the gas-liquid countercurrent contact device are: slurry product temperature 80 ° C, volatile component condensate amount (separated liquid amount) 5% (extracted extract liquid amount ratio)
The extraction rate of volatile components was 50%. Next, the extract extracted after the gas-liquid countercurrent treatment was concentrated under reduced pressure at 40 ° C. The concentrate was concentrated up to 3 times, and the obtained concentrated liquid was mixed with all the separated liquid of the volatile components to obtain a bonito-fruit concentrated extract.

【0017】また、比較例3として、揮発性成分の抽出
率が45%である以外は、実施例2と同一の条件で実施
して比較品としてのカツオ節濃縮エキスを得た。さら
に、実施例3として、濃縮の倍率が2.5倍である以外
は、実施例2と同一の条件で実施して、カツオ節濃縮エ
キスを得た。実施例2、3、比較例3で得られたカツオ
節濃縮エキスを60℃の温湯でBRIX 0.5になる
ようにそれぞれ希釈し、希釈液を専門パネラー16名に
より品質の比較評価を実施した。その結果を表2に示
す。これらの結果により、実施例2が品質的に特に優位
であることが判明した。
Further, as Comparative Example 3, a bonito-fruit-concentrated extract as a comparative product was obtained by carrying out the same conditions as in Example 2 except that the extraction rate of volatile components was 45%. Furthermore, Example 3 was carried out under the same conditions as in Example 2 except that the concentration ratio was 2.5, to obtain a bonito-fruit concentrated extract. The bonito flakes concentrated extracts obtained in Examples 2 and 3 and Comparative Example 3 were diluted with hot water at 60 ° C. so as to be BRIX 0.5, and the diluted solution was subjected to comparative evaluation of quality by 16 expert panelists. The results are shown in Table 2. From these results, it was found that Example 2 was particularly superior in terms of quality.

【0018】[0018]

【表2】 [Table 2]

【0019】[0019]

【実施例4〜6】カツオ節の微粉(粒径1mm以下)1
0重量部に、水40重量部加え、60℃まで昇温し、1
時間加熱した。その後、気液向流接触装置により揮発性
成分を抽出した。気液向流接触装置の運転条件として
は、スラリー品温60℃、揮発性成分の凝縮液量(分離
液量)5%(対スラリー比)で、揮発性成分の抽出率は
80%であった。次に、処理後のスラリーを濾布濾過、
およびセライト濾過により、カツオ節粉等の不溶固形物
を除去して清澄化し、50℃にて減圧濃縮を実施した。
処理液を2倍濃縮し、さらに、得られた濃縮液を65℃
で、5分間加熱処理した。その後、濃縮液に前記の揮発
性成分の分離液を全量混合し、カツオ節濃縮エキスを得
た。
[Examples 4 to 6] Fine powder of bonito flakes (particle size 1 mm or less) 1
40 parts by weight of water was added to 0 parts by weight, and the temperature was raised to 60 ° C., and 1
Heated for hours. Then, the volatile components were extracted by a gas-liquid countercurrent contact device. The operating conditions of the gas-liquid countercurrent contactor are: slurry temperature 60 ° C., volatile component condensate amount (separated liquid amount) 5% (ratio to slurry), and volatile component extraction rate 80%. It was Next, the treated slurry is filtered with a filter cloth,
Then, insoluble solid matter such as bonito flakes were removed and clarified by Celite filtration, and concentrated under reduced pressure at 50 ° C.
Concentrate the treatment solution twice, and further concentrate the obtained concentrate at 65 ° C.
Then, heat treatment was performed for 5 minutes. Then, the concentrated liquid was mixed with the volatile component separation liquid to obtain a bonito flakes concentrated extract.

【0020】実施例5として、濃縮後に速やかに冷却す
る以外は、実施例4と同一の条件で実施してカツオ節濃
縮エキスを得た。さらに、実施例6として濃縮の倍率が
1.8倍である以外は、実施例4と同一の条件で実施し
て、カツオ節濃縮エキスを得た。実施例4〜6で得られ
たカツオ節濃縮エキスを60℃の温湯でBRIX 0.
5になるようにそれぞれ希釈し、希釈液を専門パネラー
16名により品質の比較評価を実施した。その結果を表
3に示す。これらの結果により、実施例4が特に品質的
に優位であることが判明した。
As Example 5, a bonito-fruit-concentrated extract was obtained by carrying out under the same conditions as in Example 4, except that cooling was carried out immediately after concentration. Further, as a sixth example, a bonito-fruit concentrated extract was obtained by carrying out the same conditions as in the fourth example except that the concentration ratio was 1.8 times. The bonito flakes concentrated extracts obtained in Examples 4 to 6 were added to BRIX 0.
Each was diluted to 5 and the diluted solution was subjected to comparative evaluation of quality by 16 expert panelists. Table 3 shows the results. From these results, it was found that Example 4 was particularly superior in quality.

【0021】[0021]

【表3】 [Table 3]

【0022】[0022]

【実施例7、8】カツオ節の凍結粉砕粉10重量部に、
水30重量部加え、60℃まで昇温し、30分間加熱
し、その後、濾布濾過、セライト濾過により、カツオ節
粉等の不溶固形物を除去して、清澄化した抽出エキスを
得た。引き続き、気液向流接触装置により揮発性成分を
抽出した。気液向流接触装置の運転条件としては、抽出
エキスの品温60℃、揮発性成分の凝縮液量(分離液
量)1%(対抽出エキスの液量比)で、揮発性成分の抽
出率は70%であった。次に、気液向流装置処理後の抽
出エキスを逆浸透膜により濃縮を実施した。3倍まで濃
縮し、得られた濃縮液をペンシル型モジュールPMP−
013(旭化成工業(株)製)を用いて精密濾過処理を
行い、濾過液に前記の揮発性成分の分離液を全量混合
し、カツオ節濃縮エキスを得た。
[Examples 7 and 8] 10 parts by weight of frozen crushed bonito powder were added,
30 parts by weight of water was added, the temperature was raised to 60 ° C., and the mixture was heated for 30 minutes, after which insoluble solid matter such as skipjack kneaded powder was removed by filter cloth filtration and Celite filtration to obtain a clarified extract. Subsequently, volatile components were extracted by a gas-liquid countercurrent contact device. The operating conditions of the gas-liquid countercurrent contactor are as follows: the temperature of the extracted extract is 60 ° C., the amount of volatile component condensate (the amount of separated liquid) is 1% (the ratio of the amount of the extract to the amount of the extract) The rate was 70%. Next, the extract extracted after the gas-liquid countercurrent treatment was concentrated by a reverse osmosis membrane. Concentrate up to 3 times, and concentrate the resulting concentrate into a pencil-type module PMP-
013 (manufactured by Asahi Kasei Kogyo Co., Ltd.) was used for microfiltration, and the filtrate was mixed with the volatile component separation liquid to obtain a bonito-fruit concentrated extract.

【0023】実施例8として、濃縮を減圧濃縮で実施す
る以外は、実施例7と同一の条件で実施して比較品とし
てのカツオ節濃縮エキスを得た。実施例7、8で得られ
たカツオ節濃縮エキスを60℃の温湯でBRIX 0.
5になるようにそれぞれ希釈し、希釈液を専門パネラー
16名により品質の比較評価を実施した。その結果を表
4に示す。これらの結果により、実施例4が品質的に優
位であることが判明した。
Example 8 was carried out under the same conditions as in Example 7 except that the concentration was carried out under reduced pressure to obtain a bonito-fruit concentrated extract as a comparative product. The bonito flakes concentrated extracts obtained in Examples 7 and 8 were treated with BRIX 0.
Each was diluted to 5 and the diluted solution was subjected to comparative evaluation of quality by 16 expert panelists. The results are shown in Table 4. From these results, it was found that Example 4 was superior in quality.

【0024】[0024]

【表4】 [Table 4]

【0025】[0025]

【実施例9】煮干しの粗砕粒10重量部に、水50重量
部加え、マイコロイダーにて摩砕して、粒径約100μ
mのスラリーとし、50℃まで昇温し、20分間加熱し
た。その後、気液向流接触装置により揮発性成分を抽出
した。気液向流接触装置の運転条件としては、スラリー
品温50℃、揮発性成分の凝縮液量(分離液量)3%
(対スラリー比)で、揮発性成分の抽出率は80%であ
った。次に、濾布濾過、セライト濾過により、煮干し粉
等の不溶固形物を除去して、清澄化し、逆浸透膜により
濃縮を実施した。3倍まで濃縮し、得られた濃縮液をペ
ンシル型モジュールPMP−013(旭化成工業(株)
製)を用いて精密濾過処理を行い、濾過液に前記の揮発
性成分の分離液の80%を混合し、煮干し濃縮エキスを
得た。
[Example 9] 50 parts by weight of water was added to 10 parts by weight of coarsely crushed dried sardines, and the mixture was ground with a Mycoloider to give a particle size of about 100 μm.
m slurry, heated to 50 ° C., and heated for 20 minutes. Then, the volatile components were extracted by a gas-liquid countercurrent contact device. The operating conditions of the gas-liquid countercurrent contact device are: slurry product temperature 50 ° C, volatile component condensate amount (separated liquid amount) 3%
The extraction ratio of volatile components was 80% (ratio to slurry). Next, insoluble solids such as dried sardines were removed by filtration with a cloth filter and Celite, and the mixture was clarified and concentrated with a reverse osmosis membrane. The concentrate was concentrated up to 3 times, and the obtained concentrate was used as a pencil type module PMP-013 (Asahi Kasei Corporation).
(Manufactured by Mitsui Chemicals Co., Ltd.), and 80% of the separated liquid of the above-mentioned volatile components was mixed with the filtered liquid to obtain a concentrated extract.

【0026】実施例10として、煮干しの粗砕粒10重
量部に、水50重量部加え、マイコロイダーにて摩砕し
て、粒径約100μmのスラリーとし、60℃まで昇温
し、20分間加熱した。その後の処理を実施例9と同一
の条件で実施し、比較品としての煮干し濃縮エキスを得
た。また、比較例4として、煮干しの粗砕粒10重量部
に、水50重量部加え、マイコロイダーにて摩砕して粒
径約100μmのスラリーとし、50℃で20分間加熱
した。次に、濾布濾過、セライト濾過により、煮干し粉
等の不溶固形物を除去して、清澄化し、逆浸透膜により
濃縮を実施した。3倍まで濃縮し、得られた濃縮液をペ
ンシル型モジュールPMP−013(旭化成工業(株)
製)を用いて精密濾過処理を行い、比較品としての煮干
し濃縮エキスを得た。
As Example 10, 50 parts by weight of water was added to 10 parts by weight of coarsely crushed dried sardines, and the mixture was ground with a Mycoloider to obtain a slurry having a particle size of about 100 μm, which was heated to 60 ° C. for 20 minutes. Heated. The subsequent treatment was carried out under the same conditions as in Example 9 to obtain a dried sardine concentrated extract as a comparative product. In addition, as Comparative Example 4, 50 parts by weight of water was added to 10 parts by weight of coarsely crushed dried sardines, and the mixture was ground with a Mycoloider to obtain a slurry having a particle size of about 100 μm, and heated at 50 ° C. for 20 minutes. Next, insoluble solids such as dried sardines were removed by filtration with a cloth filter and Celite, and the mixture was clarified and concentrated with a reverse osmosis membrane. The concentrate was concentrated up to 3 times, and the obtained concentrate was used as a pencil type module PMP-013 (Asahi Kasei Corporation).
(Manufactured by Mitsui Chemical Co., Ltd.) was used for microfiltration to obtain a concentrated dried sardine extract as a comparative product.

【0027】実施例9、10、及び比較例4で得られた
煮干し濃縮エキスを60℃の温湯でBRIX 0.5に
なるようにそれぞれ希釈し、希釈液を専門パネラー16
名により品質の比較評価を実施した。その結果を表5に
示す。これらの結果により、実施例9が特に品質的に優
位であることが判明した。
The concentrated dried sardines obtained in Examples 9 and 10 and Comparative Example 4 were each diluted with hot water at 60 ° C. to BRIX 0.5, and the diluted solution was used as a specialized panel 16
Comparative evaluation of quality was carried out by name. The results are shown in Table 5. From these results, it was found that Example 9 was particularly superior in quality.

【0028】[0028]

【表5】 [Table 5]

【0029】[0029]

【発明の効果】本発明の製造方法は、節類特有の好まし
香気の保持がよく、かつ、香気、風味、特に、生臭み、
不快臭、雑味の改善された節類の濃縮エキスを容易に提
供することを可能とする。本発明で得られる濃縮エキス
は、そのまま、あるいは、一旦他の調味料、例えば、グ
ルタミン酸ナトリウム、リボヌクレオチド、蛋白加水分
解物、食塩等と混合された後、一般食品の調味料として
利用され、あるいは、噴霧乾燥、凍結乾燥すれば、節類
の好ましい香気を強く有する粉末の調味料が得られる。
INDUSTRIAL APPLICABILITY According to the production method of the present invention, the preferred aroma unique to knots is well retained, and the aroma, flavor, and particularly fishy smell,
It is possible to easily provide a concentrated extract of knotweed having an unpleasant odor and an improved taste. The concentrated extract obtained in the present invention is used as it is, or once mixed with other seasonings such as sodium glutamate, ribonucleotides, protein hydrolysates and salt, and then used as a seasoning for general food, or By spray-drying or freeze-drying, a powdery seasoning having a preferable aroma of knots can be obtained.

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】 節類と水の混合物、またはこの混合物の
抽出エキスから揮発性成分の50%以上を気液向流接触
装置によって分離液として抽出した後、前記混合物をそ
のまま使用した場合は節類の固形分を取り除き、抽出エ
キスを使用した場合はそのまま残存した液を濃縮し、該
濃縮液に前記揮発性成分の分離液を混合することを特徴
とする節類濃縮エキスの製造方法。
1. A mixture of knots and water, or 50% or more of volatile components from an extract of the mixture is extracted as a separated liquid by a gas-liquid countercurrent contactor, and the mixture is used as it is. A method for producing a concentrated extract of node-wise extract, which comprises removing the solid content of a group of compounds, concentrating the liquid remaining as it is when an extracted extract is used, and mixing the separated liquid of the volatile components with the concentrated liquid.
【請求項2】 減圧濃縮法により濃縮し、かつ濃縮倍率
が3倍以上である請求項1に記載の節類濃縮エキスの製
造方法。
2. The method for producing a concentrated extract of node-related extract according to claim 1, which is concentrated by a vacuum concentration method and has a concentration ratio of 3 times or more.
【請求項3】 減圧濃縮法により、濃縮倍率が2倍以上
になるまで濃縮し、該濃縮液を65〜85℃で5〜40
分間保持した後、揮発性成分の分離液を混合する請求項
1に記載の節類濃縮エキスの製造方法。
3. Concentration by a vacuum concentration method until the concentration ratio becomes 2 times or more, and the concentrated liquid is 5 to 40 at 65 to 85 ° C.
The method for producing a concentrated extract of node according to claim 1, wherein the separated liquid of volatile components is mixed after holding for a minute.
【請求項4】 逆浸透法により濃縮を行い、精密濾過膜
により除菌した後、揮発性成分の分離液を混合する請求
項1に記載の節類濃縮エキスの製造方法。
4. The method for producing a concentrated extract of node-related extract according to claim 1, wherein concentration is carried out by a reverse osmosis method, bacteria are sterilized by a microfiltration membrane, and then a separated liquid of volatile components is mixed.
【請求項5】 節類と水の混合物のエキス抽出から分離
液混合までの工程を50℃以下にて行う請求項5記載の
節類濃縮エキスの製造方法。
5. The method for producing a concentrated knot extract according to claim 5, wherein the steps from the extraction of the knot and water mixture to the mixing of the separated liquid are performed at 50 ° C. or lower.
【請求項6】 気液向流接触装置が、回転円錐と固定円
錐が交互に組み合わされ、被処理液が上部から薄膜状に
流下し、下部から気体が上昇する内部構造となっている
回転円錐塔である請求項1に記載の節類濃縮エキスの製
造方法。
6. A gas-liquid countercurrent contact device has an internal structure in which rotating cones and fixed cones are alternately combined, and the liquid to be treated flows down in a thin film form from the upper part and gas rises from the lower part. The method for producing a concentrated extract of node according to claim 1, which is a tower.
JP12799896A 1996-05-23 1996-05-23 Method of producing knot concentrate extract Expired - Lifetime JP3568688B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12799896A JP3568688B2 (en) 1996-05-23 1996-05-23 Method of producing knot concentrate extract

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12799896A JP3568688B2 (en) 1996-05-23 1996-05-23 Method of producing knot concentrate extract

Publications (2)

Publication Number Publication Date
JPH09308455A true JPH09308455A (en) 1997-12-02
JP3568688B2 JP3568688B2 (en) 2004-09-22

Family

ID=14973935

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006313037A (en) * 2005-05-09 2006-11-16 Yaizu Suisankagaku Industry Co Ltd Removal method of moisture and moisture removal device
JPWO2006064756A1 (en) * 2004-12-13 2008-06-12 サントリー株式会社 Method for producing coffee beverage using extracted liquid after filtration
JP2013039101A (en) * 2011-08-19 2013-02-28 Shoda Shoyu Kk Concentrated liquid seasoning

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPWO2006064756A1 (en) * 2004-12-13 2008-06-12 サントリー株式会社 Method for producing coffee beverage using extracted liquid after filtration
JP2006313037A (en) * 2005-05-09 2006-11-16 Yaizu Suisankagaku Industry Co Ltd Removal method of moisture and moisture removal device
JP4694884B2 (en) * 2005-05-09 2011-06-08 焼津水産化学工業株式会社 Moisture removal method and moisture removal device
JP2013039101A (en) * 2011-08-19 2013-02-28 Shoda Shoyu Kk Concentrated liquid seasoning

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