JP2000042406A - Production of concentrated substance - Google Patents

Production of concentrated substance

Info

Publication number
JP2000042406A
JP2000042406A JP10229518A JP22951898A JP2000042406A JP 2000042406 A JP2000042406 A JP 2000042406A JP 10229518 A JP10229518 A JP 10229518A JP 22951898 A JP22951898 A JP 22951898A JP 2000042406 A JP2000042406 A JP 2000042406A
Authority
JP
Japan
Prior art keywords
concentrated
substance
state
decompression
water
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.)
Pending
Application number
JP10229518A
Other languages
Japanese (ja)
Inventor
Shunichi Yagi
木 俊 一 八
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.)
ERII KK
Original Assignee
ERII KK
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 ERII KK filed Critical ERII KK
Priority to JP10229518A priority Critical patent/JP2000042406A/en
Publication of JP2000042406A publication Critical patent/JP2000042406A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To provide a method for producing a concentrated substance hardly affected by sterilization and scarcely damaged on the taste, the aroma, the nutrients, and the aiming extract components. SOLUTION: This method for producing a concentrated substance keeps an objective substance to be concentrated in the same state, e.g. a liquid-state, a gel state, a paste state, a powder state, a particle state, or a solid state, as it is. Alternatively, the method includes a process of removing the surface and unnecessary parts of the objective substance to be concentrated or cutting the objective substance into a prescribed size with scarce effect of oxidation. Then, the resultant objective substance is set in a pressure-decreased vessel and the pressure of the pressure-decreased vessel is controlled to be a single or a plurality of aiming vacuum degrees and heating treatment is simultaneously carried out by a controlled microwave heating or controlled far infrared heating during a part or all of the concentration process to lower the water content to an aiming level. After that, a stirring or a pulverizing and stirring process is carried out to give a product.

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、液状、ゲル状、ペ
ースト状、粉末状、粒子状又は固形状等の各種の被濃縮
物質を利用する広い産業分野、すなわち食品業界、製薬
業界、化粧品業界、香料業界や染料・顔料業界等といっ
た業界における濃縮技術分野に関する。また、一方では
各産業界において、抽出の前段階工程の技術として利用
される。
The present invention relates to a wide range of industrial fields utilizing various condensed substances such as liquid, gel, paste, powder, particle or solid, that is, the food, pharmaceutical, and cosmetic industries. The technical field relates to concentration technology in industries such as the fragrance industry and the dye / pigment industry. On the other hand, in each industry, it is used as a technology of a pre-stage process of extraction.

【0002】[0002]

【従来の技術】従来の被濃縮物質の濃縮方法としては、
まず被濃縮物質である液体又はゲル状のものを攪拌する
か、あるいはペーストや固形物質を破砕攪拌してから水
分を除去していた。また濃縮工程においても被濃縮物質
の劣化がおこるので、酸化防止剤等の保存料は水分除去
する前の固形物質を破砕攪拌した時点で投入するのが通
常であった。そして、殺菌は濃縮が終了してから行われ
るのが通常であった。
2. Description of the Related Art Conventional methods for concentrating substances to be concentrated include:
First, a liquid or gel-like substance to be concentrated is stirred or a paste or a solid substance is crushed and stirred, and then water is removed. In addition, since the substance to be concentrated deteriorates also in the concentration step, a preservative such as an antioxidant is usually added at the time of crushing and stirring the solid substance before removing water. And sterilization was usually performed after the concentration was completed.

【0003】[0003]

【発明が解決しようとする課題】従来は被濃縮物質をま
ずミキサー等により破砕攪拌し、濃縮してペーストや粒
の濃縮物質を製造していたが、これでは水分の多い時点
で破砕攪拌するので被濃縮物質に酸化が激しく起こり、
被濃縮物質の持つ本来の重要な成分を破壊していた。ま
た濃縮工程においても同様に酸化が起こり被濃縮物質の
成分破壊を起こすことがあった。そのために酸化防止剤
等の保存料を水分除去する前の破砕攪拌時点で投入する
のが通常であったが、濃縮前の多量の水分を含んだ全量
に対しての投入であるので保存料の投入量の設定に困難
があった。
Conventionally, a substance to be concentrated is first crushed and stirred by a mixer or the like, and then concentrated to produce a paste or a particle-concentrated substance. Oxidation of the substance to be concentrated occurs violently,
It had destroyed the essential components of the substance to be concentrated. Also, in the concentration step, oxidation may occur in the same manner, resulting in destruction of components of the substance to be concentrated. For this purpose, preservatives such as antioxidants were usually added at the time of crushing and stirring before removing water, but since they were added to the entire amount containing a large amount of water before concentration, the preservatives were added. There was difficulty in setting the input amount.

【0004】また従来は濃縮ペーストや濃縮粒などの被
濃縮物質の殺菌は濃縮が終了してから行うのが通常であ
ったが、熱処理によって味、香り、栄養素や抽出目的成
分が破壊されてしまうことがあった。
Conventionally, sterilization of a substance to be concentrated, such as a concentrated paste or a concentrated grain, is usually performed after the concentration is completed. However, the heat treatment destroys the taste, aroma, nutrients, and components to be extracted. There was something.

【0005】本発明は上記の点に鑑みてなされたもの
で、その目的とするところは、被濃縮物質を攪拌又は破
砕攪拌の前に本発明者が開発した水分除去技術により酸
化による成分破壊のごく少ない水分除去を大量に迅速に
行い、水分のごく少なくなった状態で攪拌又は破砕攪拌
を行い、酸化が極めて少ない水分除去が可能となり、殺
菌による濃縮物質の影響が少なく、濃縮物質の味、香
り、栄養素や抽出目的成分が破壊されてしまうことがな
い濃縮物質の製造方法を提供することにある。
[0005] The present invention has been made in view of the above-mentioned points, and an object of the present invention is to prevent the destruction of components due to oxidation by a water removal technique developed by the present inventors before stirring or crushing the substance to be concentrated. Perform very little water removal quickly in large quantities, stir or crush and stir in the state of very low water content, water removal with very little oxidation is possible, the effect of concentrated substances by sterilization is small, the taste of concentrated substances, An object of the present invention is to provide a method for producing a concentrated substance that does not destroy fragrances, nutrients, or components to be extracted.

【0006】[0006]

【課題を解決するための手段】本発明に係る濃縮物質の
製造方法は、液状、ゲル状、ペースト状、粉末状、粒子
状又は固形状等である被濃縮物質をそのままの状態とす
るか、又は該被濃縮物質が固形状である場合に表皮や不
要部分を除去した形とするか、あるいは酸化による影響
が少ないレベルの所定のサイズにカッティングした形に
し、次いで該被濃縮物質を減圧槽にセットし、該減圧槽
を単数または複数の目標減圧度に向けて圧力制御し、か
つ減圧槽内の被濃縮物質に、コントロールされたマイク
ロ波加熱とコントロールされた遠赤外線加熱を全濃縮工
程の一部または全部で同時に行う加熱処理を行ない、所
定の目標含水率まで下げ、その後に攪拌又は破砕攪拌し
て製造したものである。
The process for producing a concentrated substance according to the present invention is characterized in that the substance to be concentrated, which is in the form of a liquid, gel, paste, powder, particles or solid, is left as it is, Alternatively, when the substance to be concentrated is in a solid form, the form is such that the epidermis and unnecessary parts are removed, or the form is cut to a predetermined size at a level that is less affected by oxidation, and then the substance to be concentrated is placed in a vacuum tank. The decompression tank is pressure-controlled to one or a plurality of target decompression degrees, and controlled microwave heating and controlled far-infrared heating are applied to the substance to be concentrated in the decompression tank in one of the total concentration steps. It is manufactured by performing a heat treatment that is performed simultaneously in all or some parts, lowering the water content to a predetermined target moisture content, and then stirring or crushing and stirring.

【0007】また、本発明に係る濃縮物質の製造方法
は、固形状の被濃縮物質の場合は上記減圧槽にセットす
る前に、被濃縮物質をそのままの形か、もしくは表皮や
不要部分を除去した形か、又は酸化の発生が少ないレベ
ルの所定のサイズにカッティングした形において殺菌し
たものである。
In the method for producing a concentrated substance according to the present invention, in the case of a solid substance to be concentrated, the substance to be concentrated is removed as it is, or the epidermis and unnecessary portions are removed before setting the substance in the above-mentioned vacuum tank. Or sterilized in a form that has been cut to a predetermined size with a low level of oxidation.

【0008】[0008]

【作用】まず、野菜や果物や魚介類等の被濃縮物質が固
形の場合、そのままの形か、表皮や不要部分を除去した
形か、または酸化による影響を少なくするために、2分
割とか4分割等の大きなサイズにカッティングした形の
ままでエタノール等の殺菌液に浸けるかスプレーするか
等の方法で殺菌を行う。菌は被濃縮物質である固形物質
の表皮およびその近辺に存在すると考えられるので、こ
の段階で殺菌を行えば固形物質の品質劣化を殆ど起こさ
ないで殺菌ができる。
First, when the substance to be concentrated, such as vegetables, fruits, and seafood, is solid, it can be used as it is, with the skin or unnecessary parts removed, or divided into two parts to reduce the effects of oxidation. Sterilization is carried out by immersing or spraying in a sterilizing solution such as ethanol while keeping the cut into a large size such as divided. Bacteria are considered to be present in the epidermis of the solid substance to be concentrated and in the vicinity thereof. Therefore, if sterilization is performed at this stage, the solid substance can be sterilized with almost no quality deterioration.

【0009】一方、酸化による影響を少なくするために
2分割とか4分割等の大きなサイズにカッティングした
被濃縮物質の場合はこれらをそのままエタノール等の殺
菌液に浸けるかスプレーするか等の方法で殺菌してもよ
い。しかしながら、カッティングした表面への殺菌液の
影響を考慮すると、まず被濃縮物質をそのままの形か、
または表皮や不要部分を除去した形で殺菌を行い、次に
衛生的にカッティングした方がベターである。殺菌の
際、エタノールの他にもオゾン水等の各種の殺菌液に浸
したり、またはスプレーしたりするほかにも各種の殺菌
方法が考えられるので、特定の殺菌液および殺菌方法に
は限定されない。殺菌後に被濃縮物質を減圧槽内にセッ
トする。減圧槽内においては、被濃縮物質内部への加熱
温度を減圧度制御により比較的低温度、例えば40℃以
下に調整でき、大量の水分除去に要する時間も短時間で
あるので酸化をごく低いレベルに抑えることができる。
On the other hand, in the case of a substance to be concentrated cut into a large size such as two or four in order to reduce the influence of oxidation, these are sterilized by directly immersing or spraying in a sterilizing solution such as ethanol or the like. May be. However, considering the effect of the sterilizing solution on the cut surface, first, the substance to be concentrated is in its original form,
Alternatively, sterilization is performed in a form in which the skin and unnecessary parts are removed, and then sanitary cutting is better. At the time of sterilization, in addition to ethanol, various sterilization methods are conceivable besides immersion or spraying in various sterilization solutions such as ozone water, so that it is not limited to a specific sterilization solution and a specific sterilization method. After sterilization, the substance to be concentrated is set in a vacuum tank. In the decompression tank, the heating temperature to the inside of the substance to be concentrated can be adjusted to a relatively low temperature, for example, 40 ° C. or less, by controlling the degree of decompression, and the time required for removing a large amount of moisture is also short, so oxidation is at a very low level. Can be suppressed.

【0010】減圧槽内においては、被濃縮物質が液状、
ゲル状、ペースト状、粉末状、粒子状又は固形状である
各々の場合において、被濃縮物質内部への加熱温度を減
圧度制御により比較的低温度、例えば40℃以下に調整
でき、大量の水分に要する時間も短時間であるので酸化
をごく低いレベルに抑えることができる。この水分除去
の減圧槽内における作用を説明すると、まず、減圧によ
り被濃縮物質の水分の沸点低下をはかり水分が蒸気化し
易い状況をつくる。同時に出力コントロールされたマイ
クロ波加熱と出力コントロールされた遠赤外線加熱を被
濃縮物質に行う。この場合、減圧により水分の沸点が低
下しているので、マイクロ波加熱により被濃縮物質の内
部水分を被濃縮物質の外部にごく速やかに押し出し、そ
の水分にマイクロ波加熱と遠赤外線加熱とを同時に行い
ごく速やかに蒸気化することができる。この際重要なこ
とは、減圧下であるので被濃縮物質の内部水分をごく速
やかに押し出すことができること、内部水分の移動によ
る酸化を極力抑えることができること、減圧下であるの
で酸素が極めて希薄であり被濃縮物質の表面において酸
化を発生させないですむこと、かつ被濃縮物質の表面に
出てきた水分をマイクロ波加熱と遠赤外線加熱の共同作
業でごく速やかに除去しこの水分によって被濃縮物質表
面に酸化を発生させないようにすることができること、
かつ、蒸発熱のクーリング作用によって被濃縮物質の温
度を高めないで水分除去ができることである。
In the decompression tank, the substance to be concentrated is in a liquid state,
In each case of gel, paste, powder, particle, or solid, the heating temperature to the inside of the substance to be concentrated can be adjusted to a relatively low temperature, for example, 40 ° C. or less by controlling the degree of vacuum, and a large amount of water Oxidization can be suppressed to a very low level. The operation of the water removal in the decompression tank will be described. First, the boiling point of the water of the substance to be concentrated is reduced by decompression to create a state in which the water is easily vaporized. At the same time, microwave heating with output control and far-infrared heating with output control are applied to the substance to be concentrated. In this case, since the boiling point of the water is reduced by the reduced pressure, the internal water of the substance to be concentrated is extruded very quickly to the outside of the substance to be concentrated by the microwave heating, and the microwave heating and the far-infrared heating are simultaneously performed on the water. It can be vaporized very quickly. In this case, it is important that the internal moisture of the substance to be concentrated can be extruded very quickly because of the reduced pressure, the oxidation due to the transfer of the internal moisture can be suppressed as much as possible, and the oxygen is extremely diluted because of the reduced pressure. Oxidation does not occur on the surface of the substance to be concentrated, and moisture that has come out of the surface of the substance to be concentrated is removed very quickly by the joint work of microwave heating and far-infrared heating. That oxidation can not occur in the
In addition, water can be removed without increasing the temperature of the substance to be concentrated by the cooling action of the heat of evaporation.

【0011】また、減圧度による水の沸点がマイクロ波
と遠赤外線による被濃縮物質への加熱温度とほぼ均衡す
ることを、ファイバー温度計による実験観察によって確
認している。たとえば、減圧度40torrにて濃縮を
行えば、被濃縮物質への加温温度はほぼ34℃を維持で
きることとなる。なぜならば、濃縮においては基本的に
水分が十分存在し蒸発熱による被濃縮物質へのクーリン
グ作用が連続的に働くので、各々の減圧度における水沸
点と被濃縮物質への加熱温度はほぼ均衡するのである。
このことはさらに、減圧度制御により被濃縮物質への加
熱温度を制御できるということを意味する。かくして酸
化が極めて少ない良質の濃縮物質を得ることができる。
Further, it has been confirmed by experimental observation with a fiber thermometer that the boiling point of water due to the degree of reduced pressure is substantially balanced with the heating temperature of the substance to be concentrated by microwaves and far infrared rays. For example, if concentration is performed at a reduced pressure of 40 torr, the heating temperature of the substance to be concentrated can be maintained at approximately 34 ° C. Because, in concentration, there is basically sufficient water and cooling action on the substance to be concentrated by the heat of evaporation works continuously, so that the water boiling point and the heating temperature to the substance to be concentrated at each degree of reduced pressure are almost balanced. It is.
This further means that the heating temperature to the substance to be concentrated can be controlled by controlling the degree of pressure reduction. Thus, a high-quality concentrated substance with very little oxidation can be obtained.

【0012】[0012]

【発明実施の形態】本発明で、被濃縮物質の水分除去を
行うのには、図2に示す加熱処理装置により行う。図1
は本発明に係る濃縮工程を示す概略説明図である。減圧
槽1でのマイクロ波加熱装置及び遠赤外線加熱装置の各
仕様は次の通りである。マイクロ波5kw、遠赤外線ヒ
ーター650w×6本=3.9kw、ポンプ5.5kw
を使用した。1は減圧槽である。2は減圧槽1内にセッ
トした遠赤外線ヒーターで、通常、減圧槽1の天井面、
床面、両側面の4箇所にセットされる。減圧度の設定は
減圧槽1の外に設置した真空ポンプ3に配管した途中の
減圧弁4および減圧調整弁5を用い、減圧槽1内に通じ
る減圧口6を通して行われる。マイクロ波の減圧槽1へ
の投入は減圧槽1の外に設置したマイクロ波パワーユニ
ット7、アイソレータ8および二股に分岐した導波管9
を介して減圧槽1内のマイクロ波投入口10の2箇所よ
り行う。11は均一加熱を行うためのスターラである。
12は減圧槽1内に設置した収納棚で、プレートまたは
トレー13を多段的に収納し得るようにしている。
DESCRIPTION OF THE PREFERRED EMBODIMENTS In the present invention, the removal of water from a substance to be concentrated is performed by a heat treatment apparatus shown in FIG. FIG.
FIG. 2 is a schematic explanatory view showing a concentration step according to the present invention. The specifications of the microwave heating device and the far-infrared heating device in the decompression tank 1 are as follows. Microwave 5kw, far infrared heater 650w x 6 = 3.9kw, pump 5.5kw
It was used. 1 is a decompression tank. Reference numeral 2 denotes a far-infrared heater set in the decompression tank 1, which is usually a ceiling surface of the decompression tank 1,
It is set at four places on the floor and both sides. The degree of decompression is set through a decompression port 6 communicating with the decompression tank 1 by using a decompression valve 4 and a decompression adjustment valve 5 in the middle of a vacuum pump 3 installed outside the decompression tank 1. The microwaves are introduced into the decompression tank 1 by a microwave power unit 7, an isolator 8, and a bifurcated waveguide 9 installed outside the decompression tank 1.
Through two locations of the microwave inlet 10 in the decompression tank 1. Reference numeral 11 denotes a stirrer for performing uniform heating.
Reference numeral 12 denotes a storage shelf installed in the decompression tank 1 so that the plate or the tray 13 can be stored in multiple stages.

【0013】[0013]

【実施例】実施例1 液状の乳酸菌酵素液の濃縮を行った。これは栄養食品に
用いられる材料であり、まず濃縮ペーストを製作した後
に加工を施される原材料である。乳酸菌酵素液の含水率
は約60%であり、濃縮過程での突沸を防止するため、
マイクロ波の出力を1kwとし、遠赤外線の出力も2k
wとした。乳酸菌酵素液3kgを上下、七つのプレート
13に分割搭載し、減圧槽にセットした。減圧を開始す
ると同時にマイクロ波加熱と遠赤外線加熱を開始した。
減圧度調整の中心域をこれも乳酸菌酵素液の突沸を防止
するために50torr前後とし、濃縮を進めた。50
分後に運転を停止し、乳酸菌酵素液の濃縮後の重量を測
定したところ、1460gであった。濃縮前の乳酸菌酵
素液は、水分量約1800gであり、固体量約1200
gであったので、約1540gの水分を除去したことと
なる。濃縮完了後の乳酸菌酵素液の含水率は、260÷
1460により、約17.8%であった。加熱中心温度
域は、減圧度約50torrにより、約38℃であった
と言える。後の検査により乳酸菌はほとんど破壊されて
おらず、濃縮乳酸菌酵素液として従来になく良質である
ことが判明した。
Example 1 A liquid lactic acid bacterium enzyme solution was concentrated. This is a material used for nutritional foods, and is a raw material that is processed after first producing a concentrated paste. The water content of the lactic acid bacteria enzyme solution is about 60%, and to prevent bumping during the concentration process,
Output of microwave is 1kw, output of far infrared ray is 2k
w. 3 kg of the lactic acid bacterium enzyme solution was separately mounted on the upper and lower seven plates 13 and set in a vacuum tank. Microwave heating and far-infrared heating were started simultaneously with the start of depressurization.
The central area of the pressure reduction was adjusted to about 50 torr in order to prevent bumping of the lactic acid bacterium enzyme solution, and the concentration was advanced. 50
After one minute, the operation was stopped, and the weight of the lactic acid bacteria enzyme solution after concentration was measured to be 1460 g. The lactic acid bacteria enzyme solution before concentration has a water content of about 1800 g and a solid content of about 1200 g.
g, so that about 1540 g of water was removed. The water content of the lactic acid bacteria enzyme solution after the concentration was completed was 260 ÷
By 1460, it was about 17.8%. It can be said that the heating center temperature range was about 38 ° C. due to the degree of pressure reduction of about 50 torr. Subsequent examination showed that the lactic acid bacteria were hardly destroyed, indicating that the concentrated lactic acid bacteria enzyme solution was of higher quality than ever before.

【0014】実施例2 ゲル状の茜色素(madder pigment)の濃縮を行った。こ
れは主に食品の発色剤として用いられる色素であり、含
水率は約75%でゲル状を呈している。茜色素5kgを
上下、七つのプレート13に分割搭載し、減圧槽にセッ
トした。減圧を開始すると同時にマイクロ波を出力3k
wにて発振し、遠赤外線を出力3.9kwにて同時発振
した。40分後にマイクロ波加熱を停止し、減圧を遠赤
外線のみで減圧を高め、さらに水分除去した後に運転を
停止した。濃縮後の茜色素を計量したところ、1750
gであった。初期の水分量は約3750g、茜色素の固
体量は約1250gであり、濃縮後の水分量は約500
gであるので、約3250gの水分を除去したこととな
る。したがって、濃縮後の茜色素の含水率は、500÷
1750により、約28.6%である。この濃縮工程に
おける減圧度中心域は、30torrであったので約2
9℃程度の加熱温度域で濃縮が行われたことになる。後
の色素のスペクトル検査において、ほとんど破壊された
色域がないことが判明した。
Example 2 A gel-like madder pigment was concentrated. This is a pigment mainly used as a coloring agent for foods, and has a water content of about 75% and is in a gel state. 5 kg of the Akane dye was divided and mounted on seven plates 13 vertically and vertically, and set in a decompression tank. Microwave output 3k at the same time as decompression starts
w, and far infrared rays were simultaneously oscillated at an output of 3.9 kw. After 40 minutes, the microwave heating was stopped, the pressure was reduced only by far infrared rays, and the operation was stopped after further removing water. When the Akane pigment after concentration was measured, it was 1750
g. The initial water content is about 3750 g, the solid content of the Akane pigment is about 1250 g, and the water content after concentration is about 500 g.
g, which means that about 3250 g of water has been removed. Therefore, the water content of the Akane pigment after concentration is 500 kg.
According to 1750, it is about 28.6%. The central area of the degree of reduced pressure in this concentration step was 30 torr, so
This means that concentration was performed in a heating temperature range of about 9 ° C. Subsequent spectral inspection of the dye showed that there was almost no destroyed color gamut.

【0015】実施例3 ペースト状の生ウニ(raw gonads)の濃縮を行った。こ
れはピツァやスパゲッティー、またはシーフード系の料
理に高級スパイスとして用いられる材料で、その微妙な
味や香りは人工では製作が困難であるとされている。生
ウニの含水率は約72%であり、5kgのペースト状の
生ウニを上下、七つのプレート13に分割搭載し、減圧
槽にセットした。減圧開始と同時にマイクロ波5kw、
遠赤外線3.9kwにて運転を開始した。30分後に運
転を停止し、濃縮された生ウニペーストの重量を測定し
たところ、2100gであった。濃縮前の生ウニは、水
分量は約3600g、固体量約1400gにより構成さ
れていたので、濃縮により、約2900gの水分量を除
去したこととなる。したがって、濃縮後の含水率は、7
00÷2100により、約33%であった。この濃縮工
程における減圧度中心域は、45torrであったので
約36℃程度の加熱温度域にて濃縮が行われたことにな
る。香り、味、色ともに極めて良好な濃縮生ウニペース
トを得ることができた。
EXAMPLE 3 Raw sea urchins (raw gonads) were concentrated. It is used as a fine spice in pizza, spaghetti or seafood dishes, and its subtle taste and aroma are said to be difficult to make artificially. The water content of the raw sea urchin was about 72%, and 5 kg of paste-like raw sea urchin was separately mounted on the upper and lower seven plates 13 and set in a vacuum tank. Microwave 5kw at the same time as the decompression start,
The operation was started with 3.9 kw far infrared rays. After 30 minutes, the operation was stopped, and the weight of the concentrated raw sea urchin paste was measured to be 2,100 g. Since the raw sea urchin before concentration had a water content of about 3600 g and a solids content of about 1400 g, about 2900 g of water was removed by concentration. Therefore, the water content after concentration is 7
According to 00 ÷ 2100, it was about 33%. Since the central area of the degree of pressure reduction in this concentration step was 45 torr, it means that concentration was performed in a heating temperature range of about 36 ° C. It was possible to obtain a concentrated raw sea urchin paste having extremely good aroma, taste and color.

【0016】実施例4 イチゴのへた取り処理を行い、10kgの処理後のイチ
ゴを減圧槽1内にセットした。初期段階の水分量は10
kg×90.1%により約9.01kgと想定される。
また固体重量は約0.99kgと想定される。減圧槽1
内の減圧度は45torr前後にコントロールした。マ
イクロ波の出力を5kw、遠赤外線の出力を3.9kw
とした。イチゴへの内部加熱温度は減圧度を45tor
r前後の下で36℃前後を中心温度域とした。50分後
に減圧槽1から取り出し重量を測定したところ3.35
kgであった。したがってこの段階での成分内容は、イ
チゴ固体0・99kg、水分2.36kgであり、除去
した水分量は6.65kgであった。これをミキサーに
て破砕攪拌したところ、極めて美味で芳香なイチゴペー
ストができあがった。また、分析により100gあたり
70mgのビタミンCが検出されており、栄養素の保存
率が極めて高度であることが判明した。
Example 4 Strawberries were scraped, and 10 kg of the treated strawberries were set in the vacuum tank 1. The initial water content is 10
It is assumed to be about 9.01 kg by kg × 90.1%.
Also, the solid weight is assumed to be about 0.99 kg. Decompression tank 1
The degree of decompression inside was controlled around 45 torr. Microwave output is 5kw, far infrared output is 3.9kw
And Internal heating temperature for strawberries is 45 torr
The center temperature range was around 36 ° C. below around r. After 50 minutes, it was taken out of the vacuum tank 1 and its weight was measured.
kg. Therefore, the contents of the components at this stage were 0.99 kg of strawberry solids, 2.36 kg of water, and the amount of water removed was 6.65 kg. When this was crushed and stirred by a mixer, an extremely delicious and aromatic strawberry paste was completed. In addition, 70 mg of vitamin C was detected per 100 g by analysis, and it was found that the preservation rate of nutrients was extremely high.

【0017】実施例5 葉部分を除去したニンジン10kgを表面に数本のスリ
ットを入れ減圧槽1内にセットした。初期段階の水分量
は10kg×90.4%により約9.04kgと想定さ
れる。また固体重量は約0.96kgと想定される。減
圧槽1内の減圧度は45torr前後にコントロールし
た。マイクロ波の出力は5kw、遠赤外線の出力を3.
9kwとした。ニンジンへの内部加熱温度は減圧度を4
5torr前後の下で36℃前後を中心温度域とした。
50分後に減圧槽1から取り出し重量を測定したところ
3.55kgであった。したがってこの段階での成分内
容は、ニンジン固体0.96kg、水分2.59kgで
あり、除去した水分量は6.45kgであった。これを
ミキサーで粉砕攪拌したところ、きわめて色鮮やかで美
味な濃縮粒ができあがった。ニンジン単体の場合はペー
ストにはならずに濃縮粒となったのであるが、これをイ
チゴ等の他種のペーストと合わせ粉砕攪拌すれば、ブレ
ンドされた濃縮ペーストが生成される。
Example 5 10 kg of carrots from which leaves were removed were set in the vacuum tank 1 with several slits formed on the surface. The water content in the initial stage is assumed to be about 9.04 kg by 10 kg × 90.4%. Also, the solid weight is assumed to be about 0.96 kg. The degree of decompression in the decompression tank 1 was controlled at around 45 torr. The microwave output is 5 kW, and the far infrared output is 3.
9 kW. Internal heating temperature for carrots is 4
The center temperature range was about 36 ° C. under about 5 torr.
After 50 minutes, it was taken out of the vacuum tank 1 and its weight was measured to be 3.55 kg. Therefore, the content of the components at this stage was 0.96 kg of solid carrots and 2.59 kg of water, and the amount of water removed was 6.45 kg. When this was pulverized and stirred by a mixer, extremely colorful and delicious concentrated granules were obtained. In the case of a carrot alone, it was not a paste but a concentrated granule. If this was combined with another kind of paste such as strawberry and crushed and stirred, a blended concentrated paste was produced.

【0018】実施例6 へたを除去したトマト10kgをエタノールに1 分間浸
し、殺菌を行った。これを殺菌したトレイに搭載し減圧
槽1内にセットした。初期段階の水分量は10kg×9
5%により約9.5kgと想定される。また固体重量は
約0.5kgと想定される。減圧槽1内の減圧度は45
torr前後にコントロールした。マイクロ波の出力を
5kw、遠赤外線の出力を3.9kwとした。トマトへ
の内部加熱温度は減圧度を45torr前後の下で36
℃前後を中心域とした。55分後に減圧槽1から取り出
し重量を測定したところ2.65kgであった。したが
ってこの段階での成分内容は、トマト固体約0.5k
g、水分約2.15kgであり、除去した水分量は7.
35kgであった。これに保存料として重量比0.5%
のアスコルビン酸を添加し、殺菌したミキサーで破砕攪
拌したところ、極めて美味で芳香なトマトペーストがで
きあがった。また、分析により細菌数(生菌数)を1.
5×102 のレベルにすることができた。4℃の冷蔵保
存を行い1ヶ月後に菌分析を行ったところ菌の増殖は認
められなかった。また、美味芳香をそのまま維持してい
た。
Example 6 10 kg of tomatoes from which debris had been removed were immersed in ethanol for 1 minute and sterilized. This was mounted on a sterilized tray and set in the vacuum tank 1. Initial stage water content is 10kg x 9
5% is assumed to be about 9.5kg. Also, the solid weight is assumed to be about 0.5 kg. The degree of decompression in the decompression tank 1 is 45
Control was performed before and after torr. The microwave output was set to 5 kw, and the far infrared output was set to 3.9 kw. The internal heating temperature of the tomato was 36 degrees under a reduced pressure of around 45 torr.
The center area was around ° C. 55 minutes later, it was taken out of the vacuum tank 1 and its weight was measured to be 2.65 kg. Therefore, the ingredient content at this stage is tomato solid about 0.5k
g and water content are about 2.15 kg, and the amount of water removed is 7.
It was 35 kg. 0.5% by weight as a preservative
Was added, and the mixture was crushed and stirred with a sterilized mixer. As a result, an extremely delicious and aromatic tomato paste was produced. In addition, the number of bacteria (the number of viable bacteria) was determined to be 1.
The level was 5 × 10 2 . After refrigerated storage at 4 ° C. and analysis of the bacteria one month later, no bacterial growth was observed. Moreover, the delicious aroma was maintained as it was.

【0019】[0019]

【発明の効果】本発明に係る濃縮物質の製造方法は、ま
ず、細かなカッティング等の処理を行わずに、被濃縮物
質をそのままの形、またはそれに近い形で水分を急速に
大量に除去していくことで酸化を防止することができ
る。減圧槽内で被濃縮物質に対してマイクロ波加熱と遠
赤外線加熱の同時加熱処理を行うことにより被濃縮物質
の水分を除去していく際に、被濃縮物質への内部加熱温
度を減圧度制御により比較的低温度、例えば40℃以下に
コントロールできるので酸化の発生レベルを低くおさえ
ることができる。被濃縮物質を所定の水分量を除去した
後に減圧槽から取り出し攪拌又は破砕攪拌する際には、
被濃縮物質の初期水分の相当量をすでに除去しているの
で酸化が起こる率はごく低い。その結果、被濃縮物質の
有効成分のほとんどを残した優秀な濃縮物質ができあが
る。また、得られた濃縮物質は味、香りが損なわれるこ
となく、かつ栄養素や抽出目的成分もほとんど破壊され
ない。
According to the method for producing a concentrated substance according to the present invention, first, the substance to be concentrated is rapidly removed in a large amount in the form as it is or close to it without performing fine treatment such as cutting. By doing so, oxidation can be prevented. Controlling the internal heating temperature of the substance to be concentrated when removing moisture from the substance to be concentrated by simultaneously heating the substance to be concentrated in the vacuum tank with microwave heating and far-infrared heating As a result, the temperature can be controlled to a relatively low temperature, for example, 40 ° C. or lower, so that the generation level of oxidation can be kept low. When removing the substance to be concentrated from the vacuum tank after removing a predetermined amount of water and stirring or crushing and stirring,
Oxidation occurs at a very low rate because a significant amount of the initial moisture of the substance to be concentrated has already been removed. As a result, an excellent concentrated substance that leaves most of the active ingredients of the substance to be concentrated is produced. In addition, the obtained concentrated substance does not impair the taste and aroma, and almost no nutrients and extraction target components are destroyed.

【0020】本発明に係る濃縮物質の製造方法は、極め
て簡単であり低コストでの大量生産が可能である。ま
た、被濃縮物質が固形状の場合はそのままの状態、もし
くはそれに近い状態で=水分除去を行うことができるの
で、初期に殺菌を行い、被濃縮物質を減圧槽に投入中に
はさらにマイクロ波による殺菌を行い、かつ衛生的に攪
拌又は破砕攪拌およびパッケージを行えば極めて衛生的
な濃縮物質が容易に製造できる。
The method for producing a concentrated substance according to the present invention is extremely simple and enables mass production at low cost. In addition, when the substance to be concentrated is in a solid state or in a state close to it, water can be removed. Therefore, sterilization is performed at an initial stage, and the microwave is further added while the substance to be concentrated is put into the decompression tank. If sterilization is carried out and agitated or crushed and agitated and packaged hygienically, an extremely hygienic concentrated substance can be easily produced.

【0021】また本発明は、特に製薬業界や化粧品業界
においては成分抽出の前段階工程としての濃縮技術が非
常に重要であり、当該技術における精度の高い濃縮技術
により、成分抽出技術にも多大の貢献をすることとな
る。
In the present invention, especially in the pharmaceutical industry and the cosmetics industry, a concentration technique as a pre-step of component extraction is very important. Will make a contribution.

【図面の簡単な説明】[Brief description of the drawings]

【図1】本発明の一実施例を示す被濃縮物質の濃縮工程
を示すブロック図である。
FIG. 1 is a block diagram showing a step of concentrating a substance to be concentrated, showing one embodiment of the present invention.

【図2】被濃縮物質を濃縮する装置の概略説明図であ
る。
FIG. 2 is a schematic explanatory view of an apparatus for concentrating a substance to be concentrated.

【符号の説明】[Explanation of symbols]

1 減圧槽 2 遠赤外線ヒー
ター 3 真空ポンプ 4 減圧弁 5 減圧調整弁 6 減圧口 7 マイクロ波パワーユニット 8 アイソレータ 9 導波管 10 マイクロ波
投入口 11 スターラ 12 収納棚 13 プレートまたはトレー
DESCRIPTION OF SYMBOLS 1 Decompression tank 2 Far infrared heater 3 Vacuum pump 4 Decompression valve 5 Decompression regulating valve 6 Decompression port 7 Microwave power unit 8 Isolator 9 Waveguide 10 Microwave inlet 11 Stirrer 12 Storage shelf 13 Plate or tray

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) F26B 23/04 F26B 23/04 B Fターム(参考) 3L113 AA01 AB06 AC10 AC13 AC24 AC45 AC46 AC58 AC59 AC67 AC85 AC90 BA03 BA36 CA08 CA16 DA04 DA06 DA11 DA21 DA24 DA25 4B022 LA05 LA06 LB06 LF01 LQ06 LQ07 LQ09 LT04 LT05 4D076 AA02 AA07 AA24 BA50 DA24 DA27 EA01Y EA14Y HA11 HA20 JA03 4G075 AA22 AA61 BB01 BB10 CA26 CA35 CA65 EA01 EA05 EB01──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) F26B 23/04 F26B 23/04 B F-term (Reference) 3L113 AA01 AB06 AC10 AC13 AC24 AC45 AC46 AC58 AC59 AC67 AC85 AC90 BA03 BA36 CA08 CA16 DA04 DA06 DA11 DA21 DA24 DA25 4B022 LA05 LA06 LB06 LF01 LQ06 LQ07 LQ09 LT04 LT05 4D076 AA02 AA07 AA24 BA50 DA24 DA27 EA01Y EA14Y HA11 HA20 JA03 4G075 AA22 AA61 BB01 BB10 CA01 CA35

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 液状、ゲル状、ペースト状、粉末状、粒
子状又は固形状等である被濃縮物質をそのままの状態と
するか、又は該被濃縮物質が固形状である場合に表皮や
不要部分を除去した形とするかあるいは酸化による影響
が少ないレベルの所定のサイズにカッティングした形に
し、次いで該被濃縮物質を減圧槽にセットし、該減圧槽
を単数または複数の目標減圧度に向けて圧力制御し、か
つ減圧槽内の被濃縮物質に、コントロールされたマイク
ロ波加熱とコントロールされた遠赤外線加熱を全濃縮工
程の一部または全部で同時に行う加熱処理を行ない、所
定の目標含水率まで下げ、その後に攪拌又は破砕攪拌し
て製造したことを特徴とする濃縮物質の製造方法。
1. A liquid, a gel, a paste, a powder, a particle, a solid or the like to be condensed as it is, or when the substance to be condensed is in a solid form, the skin or unnecessary A part is removed or cut into a predetermined size at a level that is less affected by oxidation. Then, the substance to be concentrated is set in a decompression tank, and the decompression tank is set to one or more target decompression degrees. Pressure control, and subjecting the substance to be concentrated in the decompression tank to a heating treatment in which a controlled microwave heating and a controlled far-infrared heating are simultaneously performed in part or all of the entire concentration step, and a predetermined target moisture content is obtained. A method for producing a concentrated substance, wherein the concentrated substance is produced by stirring or crushing and stirring.
【請求項2】 固形状の被濃縮物質を上記減圧槽にセッ
トする前に、被濃縮物質をそのままの形か、もしくは表
皮や不要部分を除去した形か、又は酸化の発生が少ない
レベルの所定のサイズにカッティングした形において殺
菌したことを特徴とする請求項1の濃縮物質の製造方
法。
2. Prior to setting a solid substance to be concentrated in the above-mentioned decompression tank, the substance to be concentrated is in a form as it is, in a form in which skin or unnecessary portions are removed, or in a predetermined level of a level at which generation of oxidation is small. 2. The method for producing a concentrated substance according to claim 1, wherein the paste is sterilized in a form cut to a size.
JP10229518A 1998-07-31 1998-07-31 Production of concentrated substance Pending JP2000042406A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10229518A JP2000042406A (en) 1998-07-31 1998-07-31 Production of concentrated substance

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Application Number Priority Date Filing Date Title
JP10229518A JP2000042406A (en) 1998-07-31 1998-07-31 Production of concentrated substance

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Publication Number Publication Date
JP2000042406A true JP2000042406A (en) 2000-02-15

Family

ID=16893436

Family Applications (1)

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

Country Link
JP (1) JP2000042406A (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005112962A1 (en) * 2004-05-21 2005-12-01 Shunichi Yagi Aloe powder, aloe juice, and method for producing the same
JP2008500023A (en) * 2004-05-21 2008-01-10 俊一 八木 Aloe powder, aloe juice and method for producing the same
US20110038906A1 (en) * 2004-05-21 2011-02-17 Shunichi Yagi Aloe powder, aloe juice, and method for producing the same
JP4871735B2 (en) * 2004-05-21 2012-02-08 俊一 八木 Aloe powder manufacturing method
US8507016B2 (en) * 2004-05-21 2013-08-13 Shunichi Yagi Aloe powder, aloe juice, and method for producing the same
WO2007029340A1 (en) * 2005-09-06 2007-03-15 Yagi, Akira Method of using aloe powder in sexual intercourse as lubricant having lubricity
JP2007195513A (en) * 2006-01-30 2007-08-09 Mayekawa Mfg Co Ltd Method and apparatus for heating/drying of thin food sheet
CN111174534A (en) * 2018-11-12 2020-05-19 齐迹科技有限责任公司 Dynamic vacuum microwave drying method for berries with shells and product
CN111578648A (en) * 2019-02-19 2020-08-25 江苏食品药品职业技术学院 Microwave heating type vacuum freeze dryer with multiple oscillation modes
CN111578648B (en) * 2019-02-19 2022-12-23 江苏食品药品职业技术学院 Microwave heating type vacuum freeze dryer with multiple oscillation modes

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