JPS5881745A - Preparation of swollen starch slurry having high fluidity - Google Patents

Preparation of swollen starch slurry having high fluidity

Info

Publication number
JPS5881745A
JPS5881745A JP56180574A JP18057481A JPS5881745A JP S5881745 A JPS5881745 A JP S5881745A JP 56180574 A JP56180574 A JP 56180574A JP 18057481 A JP18057481 A JP 18057481A JP S5881745 A JPS5881745 A JP S5881745A
Authority
JP
Japan
Prior art keywords
slurry
starch
viscosity
temperature
cooling
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
JP56180574A
Other languages
Japanese (ja)
Other versions
JPS6230202B2 (en
Inventor
Kimito Miyamoto
宮本 公人
Yuji Hirano
勇二 平野
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 Kasei Corp
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry Co Ltd
Asahi Kasei Kogyo 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 Asahi Chemical Industry Co Ltd, Asahi Kasei Kogyo KK filed Critical Asahi Chemical Industry Co Ltd
Priority to JP56180574A priority Critical patent/JPS5881745A/en
Publication of JPS5881745A publication Critical patent/JPS5881745A/en
Publication of JPS6230202B2 publication Critical patent/JPS6230202B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To prepare swollen starch slurry having high concentration and neverthless high fluidity, by heating an aqueous slurry of starch, and cooling the slurry before the viscosity of the slurry reaches a specific level. CONSTITUTION:A heating tank having the internal space of 150l and furnished with a heating and cooling coil, is charged with 85kg of water and 15kg of corn starch. The content is heated to 68 deg.C under agitation with a stirrer at about 200rpm to effect the swelling of the starch, and maintained at 68 deg.C for about 1min. When the viscosity of the slurry reaches 720cps, the cooling is started and the content is cooled to 62 deg.C in 2min. Thereafter, the content is left at the temperature for 2hr to obtain an aqueous slurry of starch having a moderate fluidity or a viscosity of 1,230cps.

Description

【発明の詳細な説明】 本発明は比較的高濃度であってもゲル化せず、良好な流
動性を保つ澱粉の膨潤粒子スラリーの製造法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a slurry of swollen starch particles that does not gel even at relatively high concentrations and maintains good fluidity.

澱粉を水スラリー中で加熱し膨潤させると、水スラリー
は粘性を増し、特にスラリー濃度が高い場合は容易にゲ
ル化してしまって鴫、もはや流動性を示さなくなる事が
知られている。その為、例えば特願昭!J−7?コロ≦
号明細書に開示されている様な外殻薄膜構造を維持しつ
つ非豪屈折性を示す膨lIi澱粉粒子を製造し乾燥させ
ようとする場合、噴−乾燥させる方法は澱粉粒子を破壊
しないと言う事から非常に有効な手段であるが、先に述
べた如く、膨潤澱粉のスラリーは増粘し品い為、非常に
低濃度でしか取扱いができなかった。従って、乾燥時の
エネルギー効率が極端に悪く、昨今のエネルギー事情か
らしても高濃度でしかも低粘性の膨潤澱粉スラリーの出
現が待たれていた。
It is known that when starch is heated and swollen in a water slurry, the water slurry increases in viscosity and, especially when the slurry concentration is high, it easily gels and no longer exhibits fluidity. For that reason, for example, Tokugansho! J-7? Coro≦
When trying to produce and dry expanded lIi starch particles that exhibit non-refractive properties while maintaining the shell thin film structure as disclosed in the specification of the patent, the spray-drying method must not destroy the starch particles. This is a very effective method, but as mentioned earlier, the slurry of swollen starch thickens and can only be used at very low concentrations. Therefore, the energy efficiency during drying is extremely poor, and considering the current energy situation, the appearance of a swollen starch slurry with high concentration and low viscosity has been awaited.

従来、この様な膨潤澱粉スラリーの増粘現象は当然であ
るとの見方が一般的であって、増粘を押え、スラリー一
度を上げる試みはなされなかった。
Conventionally, it has been generally accepted that such a thickening phenomenon of a swollen starch slurry is a natural phenomenon, and no attempt has been made to suppress the thickening and increase the slurry strength.

特開昭11−1141300号公報には、α化澱粉乾燥
品を作る際の作業性を改曽する方法が開示されている。
JP-A-11-1141300 discloses a method for improving the workability when producing dried pregelatinized starch products.

この中では、l1ll澱粉スラリーの増粘現象による流
動性悪化の間層をニーダ−等の強力な剪断力のかかる攪
拌混練機を用いる事で解決しているが、先に述べた様な
、外殻薄膜構造を保ったままの膨潤澱粉粒子を取、扱う
場合は、強力な剪断力を用いると、薄膜が破壊されてし
まうので使えなl・つた。
In this method, the problem of poor fluidity due to the thickening phenomenon of 111 starch slurry is solved by using a stirring kneader that applies strong shearing force, such as a kneader. When handling swollen starch particles that maintain their shell thin film structure, strong shearing force cannot be used because the thin film will be destroyed.

本発明者らは、かかる膨潤澱粉スラリーの加熱時におけ
る増粘を押え、スラリーの高濃度化を可能にする事を目
的に、澱粉粒の膨潤と、1ilIII澱粉スラリーの粘
度上昇との関係を詳細に検討した結果、水スラリー中の
澱粉粒の膨潤と膨潤澱粉スラリーの粘度増加現象との間
に時間的なズレがある事、又、膨潤澱粉スラリーの゛増
粘を押えるには、比較的短時間の内に澱粉の膨潤開始温
度以下にスラリ一温度を低下させればよい事を見出し、
本発明を完成した・ 本発明は、かかる知見に基づくもので、高濃度でしかも
流動性の良い膨潤澱粉スラリーを得る事を目的としてし
する。
The present inventors investigated in detail the relationship between the swelling of starch granules and the increase in viscosity of 1ilIII starch slurry, with the aim of suppressing the thickening of the swollen starch slurry during heating and making it possible to increase the concentration of the slurry. As a result of the investigation, we found that there is a time lag between the swelling of starch granules in the water slurry and the viscosity increase phenomenon of the swollen starch slurry, and that it takes a relatively short time to suppress the viscosity increase of the swollen starch slurry. They discovered that it is sufficient to lower the slurry temperature to below the starch swelling starting temperature within a certain amount of time.
The present invention has been completed. The present invention is based on this knowledge and aims to obtain a swollen starch slurry with high concentration and good fluidity.

本発明は、澱粉の水スラリーをI−潤温度まで加熱し、
澱粉をll潤させ、該水スラリーが最大限2000cp
IIまで増粘しない間に、膨潤開始温度以下に冷却する
事を特徴とする流動性が良好なjlllIjlF粉スラ
リーの製造法に関する。
The present invention involves heating a water slurry of starch to an I-water temperature;
The starch is moistened and the water slurry has a maximum of 2000 cp.
This invention relates to a method for producing a jlllIjlF powder slurry having good fluidity, which is characterized by cooling to a temperature below the swelling start temperature while the viscosity does not increase to II.

本発明の方法により製造される膨潤澱粉スラリーは、高
濃度でしかも流動性が良い為、噴霧乾燥にかけ易く、乾
燥の際のエネルギー消費も少ない。
The swollen starch slurry produced by the method of the present invention has a high concentration and good fluidity, so it can be easily spray-dried and consumes less energy during drying.

又1この方法で得られる澱粉は外殻薄膜構造を維持した
重まの非複屈折性の澱粉粉末である。
Also, the starch obtained by this method is a heavy, non-birefringent starch powder that maintains the outer thin film structure.

本発明における膨潤温度とは、生澱粉をその外殻薄膜構
造を破壊する事なく膨潤させるに十分な温度−日内の点
を言い、この温度範囲は、使用澱粉の種■、産地、製法
1等により大きく異なる。
In the present invention, the swelling temperature refers to a temperature within a day that is sufficient to swell raw starch without destroying its outer thin film structure. varies greatly depending on

又、澱粉粒子は天然産物であるから同−澱粉であっても
備前の粒子間の性質にバラツキを持っている・従って、
個々の粒子によって1flilN始する温度及び、膨潤
し過ぎて外殻薄膜構造が破袈する温度は各々員なって来
る。本発明における膨満開始温度とは、澱粉粒子中の最
初の粒子が膨潤を開始する点を言う。又、11114温
度が取り得る範囲は、膠l1lN始濃度から最初の粒子
の外殻薄膜構造が破―するまでの温度範囲内の任意の点
であって、目的に応じてこの範囲内で選ばれる。これは
、澱粉粒子/@の1111FM始時期はほぼ温度のみに
依存し加熱時開の影響は非常に少ないからである。従っ
て、1IIIN11!度は澱粉粒子の何割を膨潤させる
かによって決められるべきもので、その温度範囲内にお
いて自由に選択してさしつかえない。澱粉粒子はi1渭
すると、生来の複屈折性を失い非複屈折性となる。従っ
て、澱粉のWl!、非WI111は、複屈折性の有無で
判断すれば明確に解る。膨潤温度範囲は、澱粉水スラリ
ーの加熱速度によっても若干ズレるが、コーンスターチ
の場合、1例を示せば、4J”C付近から70’C付近
までと言った具合に比較的狭い温度範囲である事が多い
In addition, since starch particles are a natural product, even if they are the same starch, there are variations in the properties of Bizen particles.
The temperature at which each particle starts to swell and the temperature at which the outer thin film structure ruptures due to excessive swelling vary depending on each individual particle. The swelling start temperature in the present invention refers to the point at which the first particle in the starch particles starts swelling. Further, the possible range of the 11114 temperature is any point within the temperature range from the initial concentration of glue 111N until the outer thin film structure of the first particle is broken, and is selected within this range depending on the purpose. . This is because the 1111FM start time of starch particles/@ depends almost only on temperature, and the influence of opening during heating is very small. Therefore, 1IIIIN11! The temperature should be determined depending on what percentage of the starch particles are to be swollen, and can be freely selected within that temperature range. When starch particles are exposed to i1, they lose their inherent birefringence and become non-birefringent. Therefore, Wl of starch! , non-WI111 can be clearly determined by the presence or absence of birefringence. The swelling temperature range varies slightly depending on the heating rate of the starch-water slurry, but in the case of cornstarch, it is a relatively narrow temperature range from around 4J"C to around 70'C, to give one example. There are many.

使用澱粉は、穀類澱粉が明確な膨潤開始点を持つので、
本発明の目的に適している。根茎類の澱粉、例えば、バ
レイシ冒澱粉等は、膨潤が非常に速くコントロール困難
で、本発明の実施には適さない。コーンスターチは品質
が安定し製品毎のバラツキが少なく、本発明の効果が最
もよく現われる澱粉である。
The starch used is because grain starch has a distinct swelling starting point.
suitable for the purposes of the present invention. Rhizome starch, such as potato starch, swells very quickly and is difficult to control, and is therefore not suitable for carrying out the present invention. Cornstarch is a starch that is stable in quality and has little variation from product to product, and is the starch that best exhibits the effects of the present invention.

本発明においては、澱粉を水スラリーにして使用するが
、分散媒としての水は、必ずしも純水である必要はなく
、粘度を大幅に゛上昇させない限りにおいて若干の無機
塩、有機物等な含有していてもさしつかえなく、又、水
温も膨潤開始温度未満の温度であって、氷点以上の温度
であれば何度であってもかまわない。
In the present invention, starch is used as a water slurry, but the water used as a dispersion medium does not necessarily have to be pure water, and may contain some inorganic salts, organic substances, etc. as long as it does not significantly increase the viscosity. In addition, the water temperature may be any temperature as long as it is below the swelling starting temperature and above the freezing point.

膨満温度付近で加熱を続けると、膨潤澱粉のスラリー粘
度は上昇を続け、系の粘度が2000cpmを越えると
非常にゲル化し易くなり、冷却により増粘が押えられる
よりむしろ、ゲル化して流動性を失う事になり易い。し
かしながら、粘度の上昇初期に1lII4開始温度以下
に冷却した膨潤澱粉スラリーは、冷却終了後、粘度上昇
が押えられる。
As heating continues near the swelling temperature, the viscosity of the slurry of swollen starch continues to rise, and when the viscosity of the system exceeds 2000 cpm, it becomes extremely easy to gel, and rather than being suppressed by cooling, it gels and improves fluidity. It's easy to lose it. However, in the case of a swollen starch slurry that is cooled to below the 1lII4 starting temperature at the beginning of the increase in viscosity, the increase in viscosity is suppressed after cooling is completed.

第1wIは%/3%、/!%の各々のスラリ一温度のコ
ーンスターチを44”Cの11#lIs度で処理した時
のスラリー粘度上昇の様子と、そのスラリーを加熱温度
が64℃になると同時に冷却を開始し、2分以内に60
℃まで冷却した場合のスラリー粘度上昇率の炭化を示す
。この場合のWIIII開始温度は62℃であって、冷
却処理をすると極端に粘度上昇が押えられる事がこの図
からも判る。
The first wI is %/3%, /! % of each slurry - The increase in slurry viscosity when the cornstarch at one temperature was treated at 44"C 11#lIs degree, and the slurry was cooled as soon as the heating temperature reached 64℃, and within 2 minutes. 60
It shows carbonization of slurry viscosity increase rate when cooled to ℃. The WIII starting temperature in this case is 62° C., and it can be seen from this figure that the viscosity increase can be extremely suppressed by cooling treatment.

冷却方法に関しては、できるだけ速やかに行なう事が望
ましく、加熱スラリー中に冷水を注入して冷却する方法
、又、冷却コイルにより冷却する方法等、他のいかなる
方法による冷却手段を採ってもよいが、最低限度Q3°
C/’ykの冷却速度で冷却する事、が必要である。こ
れ以下の冷却速度の場合、冷却中にもスラリー粘度の増
加が起こり好ましくない。
Regarding the cooling method, it is desirable to do it as quickly as possible, and any other cooling method may be used, such as cooling by injecting cold water into the heated slurry or cooling with a cooling coil. Minimum Q3°
It is necessary to cool at a cooling rate of C/'yk. If the cooling rate is lower than this, the viscosity of the slurry will increase even during cooling, which is undesirable.

冷却の終点は、膨潤開始温度以下で氷点以上の点ならば
いかなる温度を採っても増粘は押えられるが、増粘を押
える効果を十分期待する場合は、膨潤開始温度より更に
j″C低い温度にするのがよい。又、あまり過度の冷却
操作は不必要なので、下限を室温付近までとするのが適
当である。氷点以下では凍結するので、当然の事ながら
実施できない。
As long as the end point of cooling is below the swelling start temperature and above the freezing point, viscosity increase can be suppressed at any temperature, but if you want to have a sufficient effect of suppressing viscosity increase, the temperature should be lower than the swelling start temperature by J″C. In addition, since excessive cooling operation is unnecessary, it is appropriate to set the lower limit to around room temperature.Of course, it cannot be carried out below the freezing point because it will freeze.

又、本発明は高濃度スラリー化を目的としている為、あ
まり低濃度のスラリーでも実際上の意味を持たない。本
発明によるスラリー粘度上昇防止効果は、最低j襲スラ
リーより現われるが、特に大きく影響するのは70%以
上のスラリー濃度においてである。又、本発明における
スラリー濃度の上限は、用いる澱粉の種類等により若干
異なり、最高コj%程度であるが、通常使用できる範囲
は約20%が上限である。これは、これ以上の濃度にお
いて粘度増加が着しく、実質上冷却処理をや゛ってもそ
の効果がないからである。
Further, since the present invention aims at producing a highly concentrated slurry, even a slurry having a very low concentration has no practical meaning. The effect of preventing an increase in slurry viscosity according to the present invention appears from the lowest slurry concentration, but the effect is particularly large at a slurry concentration of 70% or more. Further, the upper limit of the slurry concentration in the present invention varies slightly depending on the type of starch used, etc., and is at most about coj%, but the upper limit of the normally usable range is about 20%. This is because at concentrations higher than this, the viscosity increases rapidly, and even if the cooling treatment is carried out too long, it will not be effective.

澱粉水スラリーを膨潤温度付近に保った場合、鋏水スラ
リー粘度がコ000ep*まで増粘するに要す時間は、
澱粉のlll1lIIにより大きく異なるが、1例を挙
げると、コーンスターチの場合、膨潤粒子の割合を9m
1i度とする膨II潅度において、加熱時間全1C分)
トシタ時0<t≦10←0450+7°63)タタLC
はスラリーのI#l形分論0度(重量%)で表わす事が
できる。
When the starch water slurry is kept near the swelling temperature, the time required for the viscosity of the starch water slurry to increase to 000ep* is:
Although it varies greatly depending on the type of starch, for example, in the case of cornstarch, the ratio of swollen particles is 9m
Total heating time is 1C min at 1i degrees of swelling II)
Toshita time 0<t≦10←0450+7°63) Tata LC
can be expressed as I#l type fraction of slurry 0 degrees (wt%).

以下、実施例にて更に詳細に説明する。This will be explained in more detail in Examples below.

実施例1 内容積1solの加熱・冷却コイル付加熱槽中に水12
#t9、コーンスターチ/!に9を入れ、佐武式小型攪
拌機を用いて約、200rprnの回転数で攪拌しつつ
正確に41”C會で加熱し澱粉を膨潤させた。約7分間
6rCに保ち、スラリー粘度が10 epaになった時
点から冷却を開始し、2分後に4.fCまで冷却し、以
後その温度を保持したところ、1時間経過後のスラリー
粘度は9j□cps 、一時間経過後の粘度はlコ30
epHであって、適度の流動性を保っていた。このスラ
リー中の澱粉粒の約9j%は複屈折性を失い膨潤してい
たが、残り約S%は複屈折性を示していた。ちなみに、
この加熱槽でこのコーンスターチを加熱した場合の膨潤
開始点は63℃であった。
Example 1 Water 12 in a heating/cooling coil additional heat tank with an internal volume of 1 sol
#t9, cornstarch/! 9 and heated to exactly 41"C using a small Satake type stirrer at a rotation speed of about 200 rpm to swell the starch. It was kept at 6rC for about 7 minutes until the slurry viscosity reached 10 ep. After 2 minutes, the slurry was cooled to 4.fC, and the temperature was maintained thereafter.The viscosity of the slurry after 1 hour was 9j□cps, and the viscosity after 1 hour was 30.
epH, and maintained appropriate fluidity. Approximately 9J% of the starch granules in this slurry lost their birefringence and were swollen, while the remaining approximately S% exhibited birefringence. By the way,
When this cornstarch was heated in this heating tank, the swelling starting point was 63°C.

実施例コ 内容積コlのビーカー中に水tro q、コーンスター
チ /209を入れ、実験室用攪拌機を用いて3001
9mの回転数で攪拌しつつ、温水バスを使って正確に6
j℃まで加熱後60分その温度に保ったところ、スラリ
ー粘度が/11IOcpsになった。このスラリーを5
分かけて60℃まで冷却し、その温度を保ち続けたとこ
ろ、1時間後の粘度は/9tOcpt1.2時間後の粘
度は2010 cpsであって、良好な流動性を示した
。この加熱装置を使った場合の、このコーンスターチの
膨潤開始温度は62℃であった。
Example: Put water troq and cornstarch /209 into a beaker with an internal volume of 1 liter, and use a laboratory stirrer to stir the mixture to 3001.
While stirring at a rotation speed of 9m, use a hot water bath to accurately
When the slurry was heated to a temperature of J°C and kept at that temperature for 60 minutes, the viscosity of the slurry became /11IOcps. This slurry
When the mixture was cooled to 60° C. over a period of minutes and maintained at that temperature, the viscosity after 1 hour was /9 tOcpt and the viscosity after 1.2 hours was 2010 cps, indicating good fluidity. When this heating device was used, the swelling starting temperature of this cornstarch was 62°C.

実施例3 実施例コと全く同様の加熱装置及びコーンスターチを用
いて、乙O℃に加温した水900 g中に、コーンスタ
ーチioo gを入れ、69℃まで加熱後10分間その
濃度に保ったところ、スラリー粘度が約JJOep■に
なった。このスラリーを10分間がけて39℃まで冷却
した後1時間経過後のスラリー粘度を測定するとJIO
ep−であった。
Example 3 Using the same heating device and cornstarch as in Example 3, 10 g of cornstarch was added to 900 g of water heated to 69°C, and after heating to 69°C, the concentration was kept at that concentration for 10 minutes. , the slurry viscosity was approximately JJOep■. This slurry was cooled to 39℃ over 10 minutes, and the slurry viscosity was measured after 1 hour.
It was ep-.

実施例ゲ 実施例コと全く同じ装置とコーンスターチを用いて一〇
重量囁のスラリー1kgを作成し、441”Cまで加熱
しコ分間経過後のスラリー粘度は/JjOcpaであっ
た。このスラリーを30分間かけて55℃まで冷却した
。この時のスラリー粘度は/3λOcpsであった・こ
のスラ9−を2j℃の室温に1時間放置したところ、ス
ラリ一温度はJj’Cで、粘度は/!10 cpaであ
って、良好な流動性を示した。
EXAMPLE 1 Using exactly the same equipment and corn starch as in Example 3, 1 kg of slurry weighing 10 weight was prepared, heated to 441"C, and the slurry viscosity after 3 minutes was /JjOcpa. The slurry was cooled to 55°C over a period of minutes.The viscosity of the slurry at this time was /3λOcps. When this slurry 9- was left at room temperature of 2j°C for 1 hour, the slurry temperature was Jj'C and the viscosity was /! 10 cpa, indicating good fluidity.

実施例j /ノのビーカー中で加温した水11239中に小麦澱粉
7jすを入れ、ラボスターラーで30(Hplの回転1
袢しつつ10℃まで加温した。加温直後のスリー粘度は
17≦Ocpsであった。このスラリーを直ちに75分
間かけて#’Cまで冷却したところ、スラリー粘度は/
l10cp−であった。このスラリーをコrCで1時間
更に放置した後スラリー粘度を測ると/?jOcpsで
あって、良好な流動性を示した。
Example J: Add 7j of wheat starch to water 11239 warmed in a beaker of 30 (Hpl) with a laboratory stirrer.
It was heated to 10°C while covered. The three viscosity immediately after heating was 17≦Ocps. When this slurry was immediately cooled to #'C over 75 minutes, the slurry viscosity was /
It was l10cp-. After leaving this slurry in CorrC for 1 hour, the slurry viscosity was measured: /? jOcps and showed good fluidity.

比較例1 実mN/の加熱槽にコーンスターチtsq、水zs〜を
入れ、実施例1と全く同様の操作をして正確に61”C
まで加温した。61℃に到達後加熱を中止し。
Comparative Example 1 Put corn starch tsq and water zs~ into a heating tank of actual mN/, perform exactly the same operation as in Example 1, and heat to exactly 61"C.
It was heated to. Heating was stopped after reaching 61°C.

攪拌のみ続けたところ、約70分後に粘度が急上昇して
攪拌困難となった。この時のスラリ一温度は4 ? !
 ”C1粘度は110000cH以上であった。しかし
ながら、スラリー中の澱粉粒を顕微鏡で見ると、懐屈折
性粒子が約3%で、非複屈折性粒子が約9751Lあり
、しかも外殻薄膜構造を破壊された粒子は見当らなかっ
た。
When only stirring was continued, the viscosity increased rapidly after about 70 minutes, making stirring difficult. The temperature of the slurry at this time is 4? !
"The viscosity of C1 was over 110,000 cH. However, when looking at the starch particles in the slurry under a microscope, there were approximately 3% birefringent particles and approximately 9,751L non-birefringent particles, and the outer thin film structure was destroyed. No particles were found.

応用例1 取扱い物質のスラリー粘度上限が約/!00 cpsで
ある噴霧乾燥装置を用いて実施例1で得たスラリーを噴
−乾燥したところ、スラリーの流動性が良くトラブルも
なくて良好な乾燥製品が得られた。
Application example 1 The upper limit of the slurry viscosity of the handled material is approx./! When the slurry obtained in Example 1 was spray-dried using a spray drying device with a speed of 0.00 cps, a good dried product was obtained as the slurry had good fluidity and no troubles.

通常この装置で噴霧乾燥できる加熱澱粉スラリーは/1
1−が上限とされていた為、約33%の生産性上昇が可
能となった。
Normally, the heated starch slurry that can be spray dried with this equipment is /1
Since the upper limit was 1-, it became possible to increase productivity by about 33%.

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

第11iIは73重量s、is重量襲におけるコーンス
ターチスフリーの膨潤温度におけるスラリー粘度増加の
割合と、冷却処理をした場合の粘度増加の割合の違いを
示す。 特許出願人 旭化成工業株式会社
No. 11iI shows the difference between the rate of increase in slurry viscosity at the swelling temperature of cornstarch-free and the rate of increase in viscosity when subjected to cooling treatment at 73 weight s and is weight. Patent applicant: Asahi Kasei Industries, Ltd.

Claims (2)

【特許請求の範囲】[Claims] (1)、澱粉の水スラリーを膨潤温度まで加熱し、澱粉
を膨潤させ、該水スラリーが最大限コ0OOcpIまで
増粘しない間に、膨潤開始温度以下に冷却する事を特徴
とする流動性が良好な膨潤澱粉スラリーの製造法。
(1) Fluidity characterized by heating a water slurry of starch to a swelling temperature to cause the starch to swell, and cooling the water slurry to a temperature below the swelling start temperature while the water slurry does not thicken to a maximum of 0OOcpI. A method for producing a good swollen starch slurry.
(2)、冷却を03℃/分以上の冷却速度で行なう事を
特徴とする特許請求の範囲第1項記載の製造法。
(2) The manufacturing method according to claim 1, characterized in that cooling is performed at a cooling rate of 0.3° C./min or more.
JP56180574A 1981-11-11 1981-11-11 Preparation of swollen starch slurry having high fluidity Granted JPS5881745A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56180574A JPS5881745A (en) 1981-11-11 1981-11-11 Preparation of swollen starch slurry having high fluidity

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56180574A JPS5881745A (en) 1981-11-11 1981-11-11 Preparation of swollen starch slurry having high fluidity

Publications (2)

Publication Number Publication Date
JPS5881745A true JPS5881745A (en) 1983-05-17
JPS6230202B2 JPS6230202B2 (en) 1987-07-01

Family

ID=16085650

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56180574A Granted JPS5881745A (en) 1981-11-11 1981-11-11 Preparation of swollen starch slurry having high fluidity

Country Status (1)

Country Link
JP (1) JPS5881745A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPWO2005005484A1 (en) * 2003-07-11 2006-10-26 旭化成ケミカルズ株式会社 Functional starch powder

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPWO2005005484A1 (en) * 2003-07-11 2006-10-26 旭化成ケミカルズ株式会社 Functional starch powder
JP4959191B2 (en) * 2003-07-11 2012-06-20 旭化成ケミカルズ株式会社 Functional starch powder

Also Published As

Publication number Publication date
JPS6230202B2 (en) 1987-07-01

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