JP3934179B2 - Method and granulated product for granulating powder made of substance ingested into animal body - Google Patents

Method and granulated product for granulating powder made of substance ingested into animal body Download PDF

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Publication number
JP3934179B2
JP3934179B2 JP20124496A JP20124496A JP3934179B2 JP 3934179 B2 JP3934179 B2 JP 3934179B2 JP 20124496 A JP20124496 A JP 20124496A JP 20124496 A JP20124496 A JP 20124496A JP 3934179 B2 JP3934179 B2 JP 3934179B2
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powder
granulated product
particle size
hemicellulose
spray liquid
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JPH1025304A (en
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裕一 前田
太郎 高橋
正紀 小川
雄彦 伊藤
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Fuji Oil Co Ltd
Freund Corp
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Fuji Oil Co Ltd
Freund Corp
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Description

【0001】
【発明の属する技術分野】
本発明は、動物の体内へ摂取される物質の粉体を造粒する方法及び造粒物に関するものである。
【0002】
【従来の技術】
粉体の取扱い性の改良や、複数の粉体の複合化のために、粉体を結着剤の存在下で顆粒状に造粒することは広く行われている。
このような粉体の造粒方法において、その粉体が食品や医薬品等のヒトを含む動物体内へ摂取される物質からなるの場合には、その結着剤としては動物に対して高安全性のものであることが要求される。また、この場合の結着剤にとっては、高結着性でかつ低コスト性のものであることも重要な因子となる。
一方、粉体の造粒により得られる造粒物は、その使用特性の観点から、できるだけ粒度分布のシャープなものであることが要求される。
従来、粉体の造粒方法としては、結着剤の種類を含めて多種多様の方法が知られているが、粉体状の食品や医薬品等を造粒する場合には、安全性の観点から、結着剤の選定に大きな制約がある等の理由から、未だ満足し得る方法はなく、粒度分布がシャープな造粒物を効率よく得ることのできる工業的に有利な造粒法の開発が望まれている。
【0003】
【発明が解決しようとする課題】
本発明は、動物体内へ摂取される物質の粉体に対して有利に適用し得る工業的造粒方法を提供することをその課題とする。
【0004】
【課題を解決するための手段】
本発明者らは、前記課題を解決すべく鋭意研究を重ねた結果、本発明を完成するに至った。
即ち、本発明によれば、動物の体内に摂取される物質の粉体を平均粒径が100〜1500μmの粒状物に造粒する方法において、該粉体の少なくとも一部をガス分散板を通した上昇気流により流動化させて形成した粉体流動層に対し、ヘミセルロース水溶液からなるスプレー液をスプレーノズルを介して微細液滴粒子として噴霧し、該スプレー液の微細液滴粒子の存在下で複数の粉体粒子相互を付着結合させて造粒物とする造粒工程を含み、前記スプレー液粘度が3〜100mpa・sの範囲にあり、前記スプレーノズルからの噴霧により形成されたスプレー液の微細液滴粒子径が10〜200μmの範囲にあり、さらに、得られる造粒中の0.7M〜1.3M(但し、Mは造粒物の平均粒径)の粒径範囲にある粒状物の含有量が75重量%以上であることを特徴とする前記の方法が提供される。
【0005】
【発明の実施の形態】
本発明で用いる被処理原料は、動物体内へ摂取される物質の粉体であり、このような粉体には、可食性物質、生理活性物質、それらの物質に対する添加剤等が包含される。可食性物質には、炭水化物系、タンパク質系及び脂肪系のものが包含される。可食性物質の具体例としては、澱粉、ショ糖、マルトース、デキストリン、小麦粉、蛋白質、ペプチド、アミノ酸、寒天、植物繊維、コーヒー、茶、ココア、健康食品、調味料、香辛料、飼料等が挙げられる。生理活性物質としては、医薬品、ビタミン、カルシュウム塩、クロレラ、ビヒズス菌、イチョウ葉抽出物等が挙げられる。また、添加剤としては、着色剤、防腐剤、増量剤等が挙げられる。粉体は、水や有機溶媒によって付着終合する自己結着性粉体と非自己結着性粉体とに大別されるが、本発明の造粒法は、それらのいずれの粉体に対しても適用することができる。
前記粉体の平均粒径は、通常、200μm以下、好ましくは10〜100μmである。
【0006】
本発明で用いる造粒用結着剤は、水溶性ヘミセルロースであり、従来公知の物質である。この水溶性ヘミセルロースは、植物体中にセルロース等と結合して存在する多糖類からなる水不溶性の植物繊維を弱酸性下に加水分解し、水溶性となった生成物を分離することによって得ることができる。
水不溶性の植物繊維としては、大豆やパームやしなどの油糧種子の水不溶性の植物繊維及び米、麦、コーン等の穀類の水不溶性の植物繊維が用いられ、特に大豆から油脂及び蛋白質の大部分を除去した後に得られるおからを有利に用いることができる。
水不溶性の植物繊維の加水分解反応は、水不溶性の植物繊維に含まれる蛋白質の等電点近くのpH条件下に行うことが必要である。原料がおからである場合の加水分解反応は、大豆蛋白質の等電点がpH4.5付近にあるので、pH3〜7、好ましくは4〜7で行う。
このように、蛋白質の等電点付近で加水分解を行うのは、蛋白質の等電点よりかなり低いpH条件下、例えば上記のような大豆蛋白を含有するおからをpH2以下の強酸性下で加水分解を行った場合、植物繊維が分解されすぎて、かつ植物繊維と一緒に蛋白質も分解されて溶出し、一方、蛋白質を含有する水不溶性の植物繊維を蛋白質の等電点よりかなり高いpHの中性又はアルカリ性において加水分解を行った場合、蛋白質が可溶化されて植物繊維と一緒に溶出してしまうためである。
この反応の詳細については、特開平4−325058号公報、特開平3−236759号公報などに記載されている。
【0007】
加水分解反応生成物は、これを濾過あるいは遠心分離により水溶性ヘミセルロースを含む水溶液から分解されなかったセルロースなどの固形物を分離除去して、水溶性ヘミセルロース水溶液を得ることができる。
【0008】
このヘミセルロース水溶液は、ガラクトース、アラビノース、ガラクツロン酸、キシロース、フコース、グルコース、ラムノース等よりなる多糖類を含むもので、その中の主な成分はガラクトース、アラビノース及びガラクツロン酸等より成る多糖類である。なお、加水分解で得られる水溶性ヘミセルロースの成分分析結果の詳細は、前記特開平4−325058号公報に記載されている。このヘミセルロース水溶液を濃縮乾燥させることにより、固形状の水溶性ヘミセルロースが得られる。
【0009】
本発明の粉体造粒方法は、粉体の少なくとも一部をガス分散板を通過したガスの上昇気流により流動化させて形成した粉体流動層に対し、ヘミセルロース水溶液を微細液滴粒子として噴霧し、この微細液滴粒子の存在下で複数の粉体粒子相互を付着させて造粒物とする造粒工程を含む。
【0010】
図1に本発明で用いる流動層造粒装置の1例についての模式図を示す。
図1において、1は流動層造粒装置、2はガス分散板、3はガス導入管、4はガス排出管、5はヘミセルロース水溶液からなるスプレー液導入管、6はスプレー液噴霧ノズル、7はフィルター、8は熱交換器、9はバグフィルター、Fは粉体流動層を示す。
図1の装置を用いて本発明の粉体造粒を行うには、装置1内に粉体を充填した後、ガス導入管3を通して流動化用ガスを導入し、フィルター7、熱交換器8を流通させた後、ガス分散板2を介してガスを上昇気流として吹上げ、ガス分散板上の粉体を流動化させ、粉体流動層Fを形成させる。この粉体流動層Fを通過したガスは、バグフィルター9を流通させた後、ガス排出管4を通して排出する。流動化用ガスとしては、通常空気が用いられるが、他のガスであってもよい。粉体流動層Fに供給する流動化用ガスの温度は40〜100℃、好ましくは50〜90℃である。流動化用ガス温度は熱交換器8でコントロールされる。
前記のようにして形成された粉体流動層Fに対しては、スプレーノズル6を介して、配管5を通して供給されたスプレー液を噴霧する。これによって、流動化粉体はしだいに造粒化され、複数の流動化粉体粒子相互がヘミセルロースの結着作用により付着結合した造粒物となる。このような造粒方法においては、時間の経過とともに、その造粒物の粒径はしだいに増加するが、それに応じて、流動化用ガスの流速を増加させて、造粒物全体を流動状態に保持する。所定時間経過後、流動化スプレー液の噴霧を中止し、流動化用ガスの吹込みを継続させて造粒物の乾燥を行う。乾燥後、流動化用ガスの吹込みを中止し、粒状物を外部へ取出し、製品造粒物とする。この場合の造粒物の乾燥は、造粒物を外部へ取出して行うこともできる。
【0011】
前記ガス分散板は、その板面に微細な透孔を多数有するものである。この透孔の孔径(直径)は、10〜300μm、好ましくは20〜200μmである。
前記スプレーノズルにおける液噴出孔の孔径(直径)は、0.5〜3μm、好ましくは1.2〜1.8μmである。
【0012】
本発明で用いる水溶性ヘミセルロースの分子量は、その10重量%水溶液としたときの25℃における粘度を指標としたとき、10〜500mPa・s、好ましくは15〜100mPa・sの粘度を与えるような分子量である。本発明において用いるヘミセルロース水溶液の濃度は3〜15重量%、好ましくは4〜12重量%である。
前記へミセルロース水溶液には、必要に応じ、人体に無害な他の結着剤、例えば、アラビアガム、プルラン、殿粉、ヒドロキシプロピルセルロース、カルボキシメチルセルロース等の水溶性高分子を適量添加することができる。また、前記ヘミセルロース水溶液には、界面活性剤、着色剤、呈味料、香料、防腐剤、糖類等を適量加えることができる。
本発明で用いるヘミセルロース水溶液からなるスプレー液において、そのスプレー液の粘度は、3〜100mpa・s、好ましくは5〜80mpa・sである。この場合のスプレー液の粘度の調節は、温度及びヘミセルロース濃度により行うことができる。スプレー液の粘度が前記範囲を逸脱すると、スプレーノズルからの噴霧性が悪くなり、造粒性の良いスプレー液の微細液滴粒子の形成が困難になる。また、この場合には、得られる造粒物の粒度分布もブロードになる。
【0013】
本発明でガス分散板を介して上方に吹上げるガスの流速は、ガス線速度で、0.3〜3m/秒、好ましくは0.5〜2m/秒である。このガス線速度が大きくなると、粒状物の粒径が小さくなり、目的とする造粒物粒度に応じて適宜選定する。
本発明で用いるスプレー液の使用量は、乾燥ヘミセルロース換算量で、粉体100重量部当り、0.1〜10重量部、好ましくは0.2〜5重量部である。この使用量が多くなると造粒物の粒径が大きくなり、目的とする造粒物粒度に応じて適宜選定する。
また、スプレー液の供給速度は、1分間当り、粉体100重量部当りの乾燥ヘミセルロースの供給速度で、0.03〜1重量部、好ましくは0.05〜0.5重量部である。スプレー液の供給速度が前記範囲を超えるようになると、得られる造粒物の粒度分布がフロードなものになり、一方、前記範囲により小さくなると、粉体の造粒に時間がかかるようになる。
【0014】
図1に示した装置において、スプレーノズルは、複数用いるのが好ましく、また、スプレーノズルの配設位置も、粉体流動層における上部、中間部及び下部等の複数の個所であることができる。スプレーノズルとしては、慣用の液スプレーノズルが用いられるが、本発明では二流体ノズル構造のスプレーノズルの使用が好ましい。
スプレノズルから噴出させるスプレー液の微細液滴粒子の平均粒径(直径)は、5〜200μm、好ましくは10〜100μmである。その平均粒径が前記範囲を超えると、得られる造粒物の粒度分布はブロードなものになり、一方、前記範囲より小さくなると、粉体流動層から流動化用ガスとともに上方に飛散する割合が多くなり、造粒効率が低下する。
【0015】
また、図1の装置において、ガス分散板2は、回転可能なもの、例えば、ロータリーディスクであってもよい。このような回転可能なガス分散板を用いる場合、造粒物の一部が分散板上に存在するようにその流動化用ガスの流速を調節するとともに、これを回転させることにより、その板面上の造粒物を転動させ、球形状又は球形に近い形状の造粒物を得ることができる。この場合の回転速度は、30〜500m/分、好ましくは50〜300m/分が得られるような速度である。
【0016】
本発明により得られる造粒物において、その平均粒径は100〜1500μm、好ましくは150〜600μm程度であり、その粒度分布もシャープなもので、取扱い性、計量性等においてすぐれたものである。本発明の造粒物は、その平均粒径をMとすると、0.7M〜1.3Mの粒径範囲を有する粒状物の含有量は、75重量%以上、好ましくは80重量%以上である。
【0017】
本発明の方法は、造粒用結着剤として天然物由来の水溶性ヘミセルロースを用いたことから、得られる造粒物は高安全性のもので、ヒトの体内へ摂取しても害を与えることはない。
また、本発明においては、粉体を流動化させて形成させた粉体流動層に対してヘミセルロース水溶液からなるスプレー液を噴霧して粉体を造粒するとともに、そのスプレー液の粘度を3〜100mpa・sに規定し、そのスプレー液をスプレーノズルから円滑にかつ粒径均一性及び付着性の良い微細液滴粒子状に噴霧させることから、粒度分布がシャープな粒径均一性の良い造粒物を得ることができる。しかも、本発明の造粒物は機械的強度においてもすぐれている。
【0018】
【実施例】
次に本発明実施例によりさらに詳細に説明する。
なお、以下に示すスプレー液の粘度は、B型粘土計によって測定されたものである。
【0019】
実施例1
乳糖7:コーンスターチ3(重量比)の混合粉体3kgを流動層造粒装置(フローコーターFLO−5型、フロイント産業社製)に仕込み、給気温度30℃の空気を送入して粉体流動層を形成し、この粉体流動層に対し、水溶性ヘミセルロース(不二製油(株)製、ヘミロース)(10wt%水溶液の、20℃の粘度が134mPa・sのもの)の7wt%水溶液(30℃における粘度:40.5mpa・s)をスプレー液として用い、これを30℃の温度条件で80ml/分の速度で噴霧し、37分間かけて造粒した。ヘミセルロースの添加量は混合粉体に対して3.0wt%とした。得られた造粒物の平均粒子径(直径)は約150μmであり、100μm未満の微粉は17.1wt%、500μm以上の粗粒は0.5wt%であり、機械的強度(圧縮強度)及び流動性も良好であった。また、この造粒物において、その0.7M(Mは平均粒径)〜1.3M(105〜195μm)の範囲の粒状物の含有量は90wt%以上であった。
【0020】
比較例1
実施例1と同じ混合粉体5kgに、同一のヘミセルロース粉体を3.0wt%添加したものをハイスピードミキサFS・GS・25J型(深江工業株式会社製、撹拌造粒装置)に仕込み、水850gを少しづつ滴下し、15分間撹拌造粒した。得られた造粒物の平均粒子径は約130μmであり、100μm以下の微粉は25.0wt%、500μm以上の粗粒は6.3wt%であり、流動層造粒に比して粒度分布が広く、粗粒、微粉とも多かった。
【0021】
実施例2
ヘミセルロース(不二製油(株)製、ソヤファイブ・S)(10wt%水溶液の20℃での粘度が48.2mPa・sのもの)の7wt%水溶液(30℃における粘度:17.2mPa・sを使用した以外は、実施例1と同様に実験した。得られた造粒物の平均粒子径は約150μmであり、100μm以下の微粉は15.3wt%、500μm以上の粗粒は0.2wt%であった。また、この造粒物において、その0.7M〜1.3Mの範囲の粒径を有する造粒物の含有量は、90wt%以上であった。
【0022】
比較例2
実施例2で示したヘミセルロースを使用した以外は比較例1と同様にして実験した。得られた造粒物の平均粒子径は約150μmで、実施例2と同程度であったが、100μm以下の微粉は39.2wt%、500μm以上の粗粒は12.2wt%と多いものであった。
【0023】
実施例3
乳糖3kgを用いた以外は実施例1と同様に実験を行った。得られた造粒物の平均粒子径は約250μmで、100μm以下の微粉は3.2wt%、500μm以上の粗粒は3.8wt%であった。また、この造粒物において、その0.7M〜1.3Mの粒径範囲を持つ粒状物の含有量は90wt%以上であった。
【0024】
比較例3
乳糖5kgを使用した以外は比較例1と同様に実験した。得られた造粒物の平均粒子径は約250μmで、実施例3と略同じであったが、100μm以下の微粉は9.3wt%、500μmの粗粒は12.7wt%と多いものであった。
【0025】
実施例4
乳糖3kgを用いた以外は実施例2と同様にして実験を行った。得られた造粒物の平均粒子径は約360μmで、100μm以下の微粉は2.0wt%、500μm以上の粗粒は2.3wt%であった。また、この造粒物において、その0.7M〜1.3Mの範囲の粒径を有する粒状物の含有量は90wt%以上であった。
【0026】
比較例4
乳糖5kgを用いた以外は比較例2と同様に実験した。得られた造粒物の平均粒子径は約350μmで、100μm以下の微粉は10.3wt%、500μm以上の粗粒は11.1wt%と多いものであった。
【0027】
実施例5
乳糖70wt%と微結晶セルロース(アビセルFD−101)30wt%からなる混合粉体3kgを用い、ヘミセルロースの添加量を3.5wt%、噴霧速度を120ml/分、造粒時間を15分としたほか実施例1と同様に実験した。得られた造粒物の平均粒径は約250μmであり、100μm以下の微粉は1.0wt%、500μm以上の粗粒は5.9wt%であった。またこの造粒物において、その0.7M〜1.3Mの範囲の粒径を有する造粒物の含有量は90wt%以上であった。
【0028】
比較例5
実施例5において、ヘミセルロース水溶液の代りにアラビアガムの7wt%水溶液を用いた以外は同様にして実験を行った。但し、この場合の噴霧速度は80ml/分で、造粒時間は30分とした。得られた造粒物の平均粒径は約120μmであり、100μm未満の微粉は27.2wt%、500μm以上の粗粒は3.7wt%であった。即ち、この場合には、造粒効果に乏しく、粉立ちするなど取扱い上好ましいものではなかった。
【0029】
【発明の効果】
本発明によれば、造粒用結着剤と造粒方法の特定の組合せを用いるとともに、特定の造粒条件を採用したことから、ヒトを含む動物の体内に取込まれる粉体を、効率よく、かつ高い安全性をもって造粒することができる。しかも、本発明で得られる造粒物は、その粒度分布がシャープなもので、かつ機械的強度も良好で、取扱い性及び計量性においてすぐれたものである。
【図面の簡単な説明】
【図1】本発明の方法の実施に用いる造粒装置の模式図を示す。
【符号の説明】
1 流動層造粒装置
2 ガス分散板
3 ガス導入管
4 ガス排出管
5 スプレー液導入管
6 スプレー液噴霧ノズル
7 フィルター
8 熱交換器
9 バグフィルター
F 粉体流動層
[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a method for granulating a powder of a substance ingested into the body of an animal and a granulated product.
[0002]
[Prior art]
In order to improve the handleability of powder and to combine a plurality of powders, it is widely practiced to granulate the powder in the presence of a binder.
In such a granulation method of powder, when the powder is made of a substance that is ingested into the animal body including humans such as foods and pharmaceuticals, the binding agent is highly safe for animals. Is required. In addition, for the binder in this case, the high binding property and low cost are also important factors.
On the other hand, a granulated product obtained by granulation of powder is required to have a sharp particle size distribution as much as possible from the viewpoint of its use characteristics.
Conventionally, a wide variety of methods for granulating powder, including the type of binder, are known, but when granulating powdered foods, pharmaceuticals, etc., from the viewpoint of safety Therefore, there is no method that can be satisfied because there are major restrictions in the selection of the binder, and development of an industrially advantageous granulation method that can efficiently obtain a granulated product with a sharp particle size distribution. Is desired.
[0003]
[Problems to be solved by the invention]
An object of the present invention is to provide an industrial granulation method that can be advantageously applied to a powder of a substance ingested into an animal body.
[0004]
[Means for Solving the Problems]
As a result of intensive studies to solve the above problems, the present inventors have completed the present invention.
That is, according to the present invention, in a method of granulating a powder of a substance ingested into an animal body into a granular material having an average particle diameter of 100 to 1500 μm, at least a part of the powder is passed through a gas dispersion plate. A spray liquid composed of a hemicellulose aqueous solution is sprayed as fine droplet particles through a spray nozzle on a powder fluidized bed formed by fluidizing with a rising airflow, and a plurality of liquid droplets in the presence of the fine droplet particles of the spray liquid are sprayed. Including a granulation step of adhering and bonding powder particles to each other to form a granulated product, wherein the spray liquid viscosity is in the range of 3 to 100 mpa · s, and the fineness of the spray liquid formed by spraying from the spray nozzle The particle size of the droplets is in the range of 10 to 200 μm, and further in the range of 0.7M to 1.3M (where M is the average particle size of the granulated product) in the resulting granulated product. Content is 75% by weight There is provided the above method characterized by the above.
[0005]
DETAILED DESCRIPTION OF THE INVENTION
The material to be treated used in the present invention is a powder of a substance ingested into the animal body, and such powder includes edible substances, physiologically active substances, additives to these substances, and the like. Edible substances include those based on carbohydrates, proteins and fats. Specific examples of edible substances include starch, sucrose, maltose, dextrin, wheat flour, protein, peptide, amino acid, agar, plant fiber, coffee, tea, cocoa, health food, seasoning, spice, feed, etc. . Examples of the physiologically active substance include pharmaceuticals, vitamins, calcium salts, chlorella, bihizu bacteria, and ginkgo biloba extract. Examples of additives include colorants, preservatives, extenders and the like. Powders are roughly classified into self-binding powders and non-self-binding powders that adhere and terminate with water or organic solvents. The granulation method of the present invention can be applied to any of these powders. It can also be applied to.
The average particle diameter of the powder is usually 200 μm or less, preferably 10 to 100 μm.
[0006]
The granulating binder used in the present invention is water-soluble hemicellulose, which is a conventionally known substance. This water-soluble hemicellulose is obtained by hydrolyzing water-insoluble plant fibers consisting of polysaccharides that are bound to cellulose in the plant body under weak acidity and separating the water-soluble product. Can do.
Examples of water-insoluble plant fibers include water-insoluble plant fibers of oil seeds such as soybeans and palm palms, and water-insoluble plant fibers of cereals such as rice, wheat and corn. Okara obtained after removing most can be used advantageously.
The hydrolysis reaction of the water-insoluble plant fiber needs to be performed under pH conditions near the isoelectric point of the protein contained in the water-insoluble plant fiber. The hydrolysis reaction when the raw material is okara is performed at pH 3-7, preferably 4-7, because the isoelectric point of soybean protein is around pH 4.5.
As described above, the hydrolysis is performed near the isoelectric point of the protein under a pH condition that is considerably lower than the isoelectric point of the protein, for example, okara containing soybean protein as described above under strong acidity of pH 2 or less. When hydrolyzed, the plant fiber is decomposed too much and the protein is also decomposed and eluted together with the plant fiber, while the water-insoluble plant fiber containing the protein has a pH considerably higher than the isoelectric point of the protein. This is because the protein is solubilized and eluted together with the plant fiber when hydrolysis is carried out in neutral or alkaline.
Details of this reaction are described in JP-A-4-325058 and JP-A-3-236759.
[0007]
The hydrolysis reaction product is filtered or centrifuged to separate and remove solids such as cellulose that have not been decomposed from the aqueous solution containing the water-soluble hemicellulose, thereby obtaining a water-soluble hemicellulose aqueous solution.
[0008]
This hemicellulose aqueous solution contains a polysaccharide composed of galactose, arabinose, galacturonic acid, xylose, fucose, glucose, rhamnose, etc., and the main components therein are polysaccharides composed of galactose, arabinose, galacturonic acid and the like. The details of the component analysis results of the water-soluble hemicellulose obtained by hydrolysis are described in JP-A-4-325058. A solid water-soluble hemicellulose can be obtained by concentrating and drying the aqueous hemicellulose solution.
[0009]
In the powder granulation method of the present invention, an aqueous solution of hemicellulose is sprayed as fine droplet particles onto a powder fluidized bed formed by fluidizing at least a part of the powder by an ascending gas flow passing through a gas dispersion plate. And a granulation step in which a plurality of powder particles are adhered to each other in the presence of the fine droplet particles to form a granulated product.
[0010]
FIG. 1 shows a schematic diagram of an example of a fluidized bed granulator used in the present invention.
In FIG. 1, 1 is a fluidized bed granulator, 2 is a gas dispersion plate, 3 is a gas introduction tube, 4 is a gas discharge tube, 5 is a spray solution introduction tube made of a hemicellulose aqueous solution, 6 is a spray solution spray nozzle, and 7 is a spray solution spray nozzle. Filter, 8 is a heat exchanger, 9 is a bag filter, and F is a powder fluidized bed.
In order to perform the powder granulation according to the present invention using the apparatus shown in FIG. 1, after the powder is filled in the apparatus 1, a fluidizing gas is introduced through the gas introduction pipe 3, and the filter 7 and the heat exchanger 8 are introduced. After the gas is circulated, the gas is blown up as an updraft through the gas dispersion plate 2, the powder on the gas dispersion plate is fluidized, and the powder fluidized bed F is formed. The gas passing through the powder fluidized bed F is circulated through the bag filter 9 and then discharged through the gas discharge pipe 4. As the fluidizing gas, air is usually used, but other gases may be used. The temperature of the fluidizing gas supplied to the powder fluidized bed F is 40 to 100 ° C, preferably 50 to 90 ° C. The fluidizing gas temperature is controlled by the heat exchanger 8.
The powder fluidized bed F formed as described above is sprayed with the spray liquid supplied through the pipe 5 via the spray nozzle 6. As a result, the fluidized powder is gradually granulated, and a plurality of fluidized powder particles are formed into a granulated product adhered and bonded together by the binding action of hemicellulose. In such a granulation method, the particle size of the granulated product gradually increases with the passage of time, but the flow rate of the fluidizing gas is increased accordingly, and the entire granulated product is fluidized. Hold on. After a predetermined time has elapsed, the spraying of the fluidized spray liquid is stopped, and the granulated product is dried by continuing the blowing of the fluidizing gas. After drying, the blowing of the fluidizing gas is stopped, and the granular material is taken out to make a product granulated product. In this case, the granulated product can be dried by taking out the granulated product to the outside.
[0011]
The gas dispersion plate has many fine through holes on the plate surface. The hole diameter (diameter) of the through hole is 10 to 300 μm, preferably 20 to 200 μm.
The diameter (diameter) of the liquid ejection hole in the spray nozzle is 0.5 to 3 μm, preferably 1.2 to 1.8 μm.
[0012]
The molecular weight of the water-soluble hemicellulose used in the present invention is a molecular weight that gives a viscosity of 10 to 500 mPa · s, preferably 15 to 100 mPa · s, using the viscosity at 25 ° C. as a 10% by weight aqueous solution as an index. It is. The concentration of the aqueous hemicellulose solution used in the present invention is 3 to 15% by weight, preferably 4 to 12% by weight.
If necessary, the hemicellulose aqueous solution may be added with an appropriate amount of other binders that are harmless to the human body, for example, water-soluble polymers such as gum arabic, pullulan, starch, hydroxypropylcellulose, carboxymethylcellulose and the like. it can. Moreover, surfactant, a coloring agent, a flavoring agent, a fragrance | flavor, an antiseptic | preservative, saccharides, etc. can be added to the said hemicellulose aqueous solution suitably.
In the spray liquid composed of the hemicellulose aqueous solution used in the present invention, the viscosity of the spray liquid is 3 to 100 mpa · s, preferably 5 to 80 mpa · s. In this case, the viscosity of the spray liquid can be adjusted by temperature and hemicellulose concentration. When the viscosity of the spray liquid deviates from the above range, the sprayability from the spray nozzle deteriorates, and it becomes difficult to form fine droplet particles of the spray liquid with good granulation properties. In this case, the particle size distribution of the resulting granulated product is also broad.
[0013]
In the present invention, the flow rate of the gas blown upward through the gas dispersion plate is 0.3 to 3 m / second, preferably 0.5 to 2 m / second, in terms of gas linear velocity. When the gas linear velocity increases, the particle size of the granular material decreases, and is appropriately selected according to the intended granulated particle size.
The usage-amount of the spray liquid used by this invention is 0.1-10 weight part per 100 weight part of powders in dry hemicellulose conversion amount, Preferably it is 0.2-5 weight part. When the amount used is increased, the particle size of the granulated product becomes large, and it is appropriately selected according to the intended granule particle size.
Further, the supply rate of the spray liquid is 0.03 to 1 part by weight, preferably 0.05 to 0.5 part by weight, as the supply rate of dry hemicellulose per 100 parts by weight of the powder per minute. When the supply rate of the spray liquid exceeds the above range, the particle size distribution of the resulting granulated product becomes a floating one. On the other hand, when the spray rate decreases, the granulation of the powder takes time.
[0014]
In the apparatus shown in FIG. 1, it is preferable to use a plurality of spray nozzles, and the spray nozzles can be disposed at a plurality of locations such as an upper portion, an intermediate portion, and a lower portion in the powder fluidized bed. As the spray nozzle, a conventional liquid spray nozzle is used. In the present invention, it is preferable to use a spray nozzle having a two-fluid nozzle structure.
The average particle diameter (diameter) of the fine droplet particles of the spray liquid ejected from the spray nozzle is 5 to 200 μm, preferably 10 to 100 μm. When the average particle size exceeds the above range, the resulting granule has a broad particle size distribution. On the other hand, when the average particle size is smaller than the above range, the ratio of scattering upward from the powder fluidized bed with the fluidizing gas is high. Increases and granulation efficiency decreases.
[0015]
Further, in the apparatus of FIG. 1, the gas dispersion plate 2 may be a rotatable one, for example, a rotary disk. When such a rotatable gas dispersion plate is used, the flow rate of the fluidizing gas is adjusted so that a part of the granulated material exists on the dispersion plate, and the plate surface is rotated by rotating it. The above granulated product can be rolled to obtain a granulated product having a spherical shape or a shape close to a spherical shape. The rotation speed in this case is such that 30 to 500 m / min, preferably 50 to 300 m / min is obtained.
[0016]
In the granulated product obtained by the present invention, its average particle size is 100 to 1500 μm, preferably about 150 to 600 μm, its particle size distribution is sharp, and it is excellent in handleability, meterability and the like. In the granulated product of the present invention, when the average particle size is M, the content of the granular material having a particle size range of 0.7M to 1.3M is 75% by weight or more, preferably 80% by weight or more. .
[0017]
Since the method of the present invention uses water-soluble hemicellulose derived from natural products as a binder for granulation, the resulting granulated product is highly safe and can be harmful even if ingested into the human body. There is nothing.
In the present invention, the powder fluidized bed formed by fluidizing the powder is sprayed with a spray liquid composed of an aqueous hemicellulose solution to granulate the powder, and the viscosity of the spray liquid is adjusted to 3 to 3. Granulation with good particle size uniformity with a sharp particle size distribution because the spray liquid is smoothly sprayed from the spray nozzle into fine droplet particles with good particle size uniformity and adhesion. You can get things. Moreover, the granulated product of the present invention is excellent in mechanical strength.
[0018]
【Example】
Next, the embodiment of the present invention will be described in more detail.
In addition, the viscosity of the spray liquid shown below is measured with a B-type clay meter.
[0019]
Example 1
Lactose 7: 3 kg of mixed powder of corn starch 3 (weight ratio) is charged into a fluidized bed granulator (flow coater FLO-5, manufactured by Freund Sangyo Co., Ltd.), and air is supplied at an air supply temperature of 30 ° C. A fluidized bed was formed, and a 7 wt% aqueous solution of water-soluble hemicellulose (Fuji Oil Co., Ltd., hemirose) (10 wt% aqueous solution having a viscosity of 134 mPa · s at 20 ° C) was formed on the powder fluidized bed. Viscosity at 30 ° C .: 40.5 mpa · s) was used as a spray liquid, and this was sprayed at a rate of 80 ml / min under a temperature condition of 30 ° C. and granulated for 37 minutes. The amount of hemicellulose added was 3.0 wt% with respect to the mixed powder. The obtained granulated product has an average particle size (diameter) of about 150 μm, fine powder of less than 100 μm is 17.1 wt%, coarse particles of 500 μm or more is 0.5 wt%, mechanical strength (compressive strength) and The fluidity was also good. In this granulated product, the content of the granular material in the range of 0.7 M (M is an average particle size) to 1.3 M (105 to 195 μm) was 90 wt% or more.
[0020]
Comparative Example 1
A mixture obtained by adding 3.0 wt% of the same hemicellulose powder to 5 kg of the same mixed powder as in Example 1 was charged into a high-speed mixer FS / GS / 25J type (manufactured by Fukae Kogyo Co., Ltd., stirring granulator), water 850 g was added dropwise little by little, and granulated with stirring for 15 minutes. The average particle size of the obtained granulated product is about 130 μm, the fine powder of 100 μm or less is 25.0 wt%, the coarse particle of 500 μm or more is 6.3 wt%, and the particle size distribution is larger than that of fluidized bed granulation. Wide, coarse and fine.
[0021]
Example 2
7 wt% aqueous solution (viscosity at 30 ° C: 17.2 mPa · s) of hemicellulose (Fuji Oil Co., Ltd., Soya Five · S) (10 wt% aqueous solution with a viscosity at 20 ° C of 48.2 mPa · s) The average particle size of the obtained granulated product was about 150 μm, the fine powder of 100 μm or less was 15.3 wt%, and the coarse particle of 500 μm or more was 0.2 wt%. In this granulated product, the content of the granulated product having a particle size in the range of 0.7 M to 1.3 M was 90 wt% or more.
[0022]
Comparative Example 2
The experiment was performed in the same manner as in Comparative Example 1 except that the hemicellulose shown in Example 2 was used. The average particle diameter of the obtained granulated product was about 150 μm, which was about the same as Example 2. However, fine particles of 100 μm or less were 39.2 wt%, and coarse particles of 500 μm or more were 12.2 wt%. there were.
[0023]
Example 3
The experiment was performed in the same manner as in Example 1 except that 3 kg of lactose was used. The average particle size of the obtained granulated product was about 250 μm, fine powder of 100 μm or less was 3.2 wt%, and coarse particles of 500 μm or more was 3.8 wt%. In this granulated product, the content of the granular material having a particle size range of 0.7 M to 1.3 M was 90 wt% or more.
[0024]
Comparative Example 3
The experiment was performed in the same manner as in Comparative Example 1 except that 5 kg of lactose was used. The obtained granulated product had an average particle diameter of about 250 μm, which was almost the same as Example 3. However, the fine powder of 100 μm or less was 9.3 wt%, and the coarse particle of 500 μm was 12.7 wt%. It was.
[0025]
Example 4
The experiment was performed in the same manner as in Example 2 except that 3 kg of lactose was used. The average particle diameter of the obtained granulated product was about 360 μm, the fine powder of 100 μm or less was 2.0 wt%, and the coarse particle of 500 μm or more was 2.3 wt%. Moreover, in this granulated material, the content of the granular material having a particle size in the range of 0.7M to 1.3M was 90 wt% or more.
[0026]
Comparative Example 4
An experiment was conducted in the same manner as in Comparative Example 2 except that 5 kg of lactose was used. The obtained granulated product had an average particle diameter of about 350 μm, fine powders of 100 μm or less were 10.3 wt%, and coarse grains of 500 μm or more were 11.1 wt%.
[0027]
Example 5
In addition to 3 kg of mixed powder consisting of 70 wt% lactose and 30 wt% microcrystalline cellulose (Avicel FD-101), the amount of hemicellulose added was 3.5 wt%, the spray rate was 120 ml / min, and the granulation time was 15 min. The experiment was performed in the same manner as in Example 1. The average particle size of the obtained granulated product was about 250 μm, fine powder of 100 μm or less was 1.0 wt%, and coarse particle of 500 μm or more was 5.9 wt%. Further, in this granulated product, the content of the granulated product having a particle size in the range of 0.7M to 1.3M was 90 wt% or more.
[0028]
Comparative Example 5
In Example 5, an experiment was conducted in the same manner except that a 7 wt% aqueous solution of gum arabic was used instead of the aqueous solution of hemicellulose. However, the spray rate in this case was 80 ml / min, and the granulation time was 30 minutes. The obtained granulated product had an average particle size of about 120 μm, fine powders of less than 100 μm were 27.2 wt%, and coarse particles of 500 μm or more were 3.7 wt%. That is, in this case, the granulation effect is poor and it is not preferable in handling such as powdering.
[0029]
【The invention's effect】
According to the present invention, since a specific combination of a granulating binder and a granulating method is used and a specific granulating condition is adopted, a powder taken into the body of an animal including a human is efficiently used. Granulates well and with high safety. In addition, the granulated product obtained by the present invention has a sharp particle size distribution, good mechanical strength, and excellent handleability and meterability.
[Brief description of the drawings]
FIG. 1 shows a schematic view of a granulating apparatus used for carrying out the method of the present invention.
[Explanation of symbols]
DESCRIPTION OF SYMBOLS 1 Fluidized bed granulator 2 Gas dispersion plate 3 Gas introduction pipe 4 Gas discharge pipe 5 Spray liquid introduction pipe 6 Spray liquid spray nozzle 7 Filter 8 Heat exchanger 9 Bag filter F Powder fluidized bed

Claims (4)

動物の体内に摂取される物質の粉体を平均粒径が100〜1500μmの粒状物に造粒する方法において、該粉体の少なくとも一部をガス分散板を通した上昇気流により流動化させて形成した粉体流動層に対し、ヘミセルロース水溶液からなるスプレー液をスプレーノズルを介して微細液滴粒子として噴霧し、該スプレー液の微細液滴粒子の存在下で複数の粉体粒子相互を付着結合させて造粒物とする造粒工程を含み、前記スプレー液粘度が3〜100mpa・sの範囲にあり、前記スプレーノズルからの噴霧により形成されたスプレー液の微細液滴粒子径が10〜200μmの範囲にあり、さらに、得られる造粒中の0.7M〜1.3M(但し、Mは造粒物の平均粒径)の粒径範囲にある粒状物の含有量が75重量%以上であることを特徴とする前記の方法。In a method of granulating a powder of a substance ingested into an animal body into a granular material having an average particle diameter of 100 to 1500 μm, at least a part of the powder is fluidized by an ascending current through a gas dispersion plate. A spray liquid consisting of an aqueous solution of hemicellulose is sprayed as fine droplet particles through the spray nozzle to the formed powder fluidized bed, and a plurality of powder particles are adhered and bonded in the presence of the fine droplet particles of the spray liquid. Including a granulation step to form a granulated product, the spray liquid viscosity is in the range of 3 to 100 mpa · s, and the fine droplet particle diameter of the spray liquid formed by spraying from the spray nozzle is 10 to 200 μm. Furthermore, the content of the granular material in the particle size range of 0.7M to 1.3M (where M is the average particle size of the granulated product) in the obtained granulated material is 75% by weight or more. It is characterized by being Said method. 該分散板として回転可能なものを用いるとともに、これを30〜500m/分の周速が得られるように回転させ、その分散板上の造粒物を転動させる請求項1の方法。2. The method according to claim 1, wherein a rotating plate is used as the dispersing plate, and the dispersing plate is rotated so as to obtain a peripheral speed of 30 to 500 m / min, and the granulated material on the dispersing plate is rolled. 該ヘミセルロースが大豆由来のヘミセルロースである請求項1又は2の方法。The method according to claim 1 or 2, wherein the hemicellulose is soybean-derived hemicellulose. 請求項1〜3のいずれかの方法で得られた造粒物。A granulated product obtained by the method according to claim 1.
JP20124496A 1996-07-11 1996-07-11 Method and granulated product for granulating powder made of substance ingested into animal body Expired - Lifetime JP3934179B2 (en)

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JP4147622B2 (en) * 1998-05-08 2008-09-10 日油株式会社 Granulated / Coated food and production method thereof
DE60036205T2 (en) * 2000-07-27 2008-05-21 Roquette Frères Granules consisting of starch and lactose
KR100910382B1 (en) * 2007-08-16 2009-08-04 세메스 주식회사 Production device of carbon nano-tube using fluidized bed of dispersing catalysts
KR100985725B1 (en) * 2007-09-27 2010-10-07 세메스 주식회사 Apparatus and method of producting carbon nano tube
ES2546541T3 (en) 2008-03-07 2015-09-24 San-Ei Gen F.F.I., Inc. Procedure for modifying starch and procedure for producing a preparation mixed with starch
JP2015218322A (en) * 2014-05-21 2015-12-07 旭化成ケミカルズ株式会社 Fine starch particle and production method thereof
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