JPS60172344A - Preparation of microcapsule - Google Patents
Preparation of microcapsuleInfo
- Publication number
- JPS60172344A JPS60172344A JP2783484A JP2783484A JPS60172344A JP S60172344 A JPS60172344 A JP S60172344A JP 2783484 A JP2783484 A JP 2783484A JP 2783484 A JP2783484 A JP 2783484A JP S60172344 A JPS60172344 A JP S60172344A
- Authority
- JP
- Japan
- Prior art keywords
- nozzle
- component
- core component
- manufacturing
- item
- 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
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/02—Making microcapsules or microballoons
- B01J13/04—Making microcapsules or microballoons by physical processes, e.g. drying, spraying
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Manufacturing Of Micro-Capsules (AREA)
Abstract
Description
【発明の詳細な説明】 本発明はマイクロカプセルの製造法に関する。[Detailed description of the invention] The present invention relates to a method for manufacturing microcapsules.
マイクロカプセルの製造法としては従来、スプレー法や
コアセルベーション法などが知られている。これらの方
法は核成分を完全にマイクロカプセル化するのが困難で
あり、核成分が液体の場合にはこの液体がカプセル表面
に浸出する傾向があり、かつ多数のカプセルが相互に凝
集し、独立構造のカプセルを作ることは実質上不可能で
ある。Conventionally known methods for producing microcapsules include a spray method and a coacervation method. These methods have difficulty in completely microencapsulating the core component, and when the core component is liquid, this liquid tends to leach onto the capsule surface, and many capsules tend to aggregate with each other and become independent. It is virtually impossible to encapsulate the structure.
一方、核成分を完全に被覆した独立カプセルを製造する
方法としては、核成分用ノズルの外周に皮膜成分用ノス
゛ルを有する多重ノズルから核成分と皮膜成分を同時に
冷却液中に放出し、表面張力の作用によって完全被覆カ
プセルを形成させる方法が知られている。この方法では
ノズル径と表面張力との関係から500μI11以下の
カプセルを工業的に得るのは実質上不可能である。On the other hand, as a method for manufacturing independent capsules that completely cover the core component, the core component and the film component are simultaneously discharged into the coolant from a multiple nozzle having a nozzle for the film component on the outer periphery of the nozzle for the core component, and the surface tension A method of forming a completely covered capsule by the action of With this method, it is virtually impossible to industrially obtain capsules with a diameter of 500 μI11 or less due to the relationship between nozzle diameter and surface tension.
本発明は前記多重ノズルを回i17ヘツドに取すイ・j
け、遠心力の作用によって微細な独立マイクロカプセル
を製造する方法を提供する。The present invention is characterized in that the multiple nozzles are mounted on a rotary head.
The present invention provides a method for producing fine independent microcapsules by the action of centrifugal force.
即ち、本発明は核成分用ノズルおよびその外周に設けた
皮膜成分用ノズルから核成分および皮膜成分を同時に遠
心力によって皮膜成分の硬化条件下に放出することを特
徴とするマイクロカプセルの製造法に関する。That is, the present invention relates to a method for producing microcapsules, characterized in that the core component and the film component are simultaneously released from a core component nozzle and a film component nozzle provided on the outer periphery of the core component by centrifugal force under conditions for curing the film component. .
本発明マイクロカプセルを製造するに適した装置の一例
を第1図および第2図に示す。An example of an apparatus suitable for manufacturing the microcapsules of the present invention is shown in FIGS. 1 and 2.
第1図は本発明方法の実施に適した回転ヘッド(5)の
側断面図であり、第2図は回転ヘッドを下方からみた図
である。核成分用ノズル(1)は核成分タンク(6)、
皮膜成分用ノズル(2)は皮膜成分タンク(7)および
硬化剤用ノズル(3)は硬化剤タンク(8)にそれぞれ
連結し、回転ヘッド(5)に複数個配置されている。FIG. 1 is a side sectional view of a rotary head (5) suitable for carrying out the method of the present invention, and FIG. 2 is a view of the rotary head seen from below. The nuclear component nozzle (1) is a nuclear component tank (6),
The film component nozzle (2) is connected to the film component tank (7), and the curing agent nozzle (3) is connected to the curing agent tank (8), respectively, and a plurality of them are arranged on the rotating head (5).
核成分と皮膜成分とはポンプなとの供給手段によってノ
ズル先端から同時に放出され、四軒ヘッドの回転によっ
て遠心力により、ハウシング内に飛散する。その際、核
成分は皮1漠成分によってカプセル化し、かつ皮膜成分
は硬化剤用ノズルから放出される硬化剤によって硬化さ
れる。硬化剤は必ずしも硬化剤用ノズルから放出される
必要はなく、ハウタンク内部を硬化条件下に置いてもよ
い。The core component and the film component are simultaneously discharged from the nozzle tip by a supply means such as a pump, and are scattered into the housing by the centrifugal force caused by the rotation of the Shiken head. In this case, the core component is encapsulated by the skin component, and the skin component is hardened by the hardening agent discharged from the hardening agent nozzle. The curing agent does not necessarily need to be ejected from the curing agent nozzle, and the interior of the Howtank may be placed under curing conditions.
典型的には第1図に示すごとく、硬化剤用ノズルを皮膜
成分用ノズルの外周にそなえたものであり、これによっ
て、皮膜成分はノズルから放出されると同時に硬化剤と
接触しマイクロカプセル化が効率よく行なわれる。回転
ヘッドを硬化剤の液中に浸漬した状態で行なってもよい
が遠心力の作用は液による抵抗だけ小さくなり、独立し
た微少マイクロカプセルは得難くなる。ハウタンクを硬
化剤のガス雰囲気下、あるいは冷却雰囲気下で行なって
もよい。Typically, as shown in Figure 1, a hardening agent nozzle is provided around the outer periphery of a film component nozzle, whereby the film components are released from the nozzle and simultaneously come into contact with the hardening agent and become microencapsulated. is carried out efficiently. Although this may be carried out with the rotating head immersed in the curing agent liquid, the action of centrifugal force will be reduced by the resistance caused by the liquid, making it difficult to obtain independent microcapsules. Howtanking may be carried out under a hardening agent gas atmosphere or under a cooling atmosphere.
核成分としては常温または加熱状態で液状でノズルから
放出し得るものであればいかなるものでもよい。具体的
には、例えば各種医薬品水溶液、薬剤を溶解した油、香
料、化粧品、食品、工業化学薬品等が例示される。これ
らはノズルからの放出時の粘度が500cps以下、好
ましくは1〜30cI+s、 !1.jにI O−20
cI!sとなるように組成またはノズル温度を調整する
。The core component may be any material as long as it can be discharged from the nozzle in liquid form at room temperature or in a heated state. Specifically, for example, various pharmaceutical aqueous solutions, oils containing dissolved medicines, perfumes, cosmetics, foods, industrial chemicals, etc. are exemplified. These have a viscosity of 500 cps or less, preferably 1 to 30 cI+s, when discharged from the nozzle. 1. j to I O-20
cI! The composition or nozzle temperature is adjusted so that s.
皮膜成分は核成分と相溶性がなく、ノズルから放出する
ときは液体であるが、硬化後は常温で皮膜を維持し得る
ものであればよい。核成分が水溶液のときはワックス類
、硬化油、樹脂類等が適当であり、これらは硬化剤とし
て冷媒、例えば液体窒素、液体空気、氷水、161脂硬
化剤などを用いれば良い。好ましくは一20℃以下の冷
媒を用いるのがよく、特に硬化剤用ノズルからこれらの
冷媒を放出させる。核成分が油性のときは疎油性物質、
例えばゼラチン等を皮膜成分として用いてもよい。The film component is not compatible with the core component and is liquid when discharged from the nozzle, but any film component that can maintain the film at room temperature after curing may be used. When the core component is an aqueous solution, waxes, hardened oils, resins, etc. are suitable, and a refrigerant such as liquid nitrogen, liquid air, ice water, 161 fat hardening agent, etc. may be used as a hardening agent. Preferably, a refrigerant having a temperature of -20° C. or lower is used, and in particular, these refrigerants are discharged from a hardening agent nozzle. When the core component is oily, it is an oleophobic substance,
For example, gelatin or the like may be used as a film component.
さらに皮膜成分とてはポリアクリル酸水溶液等のポリマ
ー水溶液を用い、硬化剤として塩化カルシウム等の凝集
剤を用いる方法、活性水素を有する化合物を架橋剤で架
橋させる力法等種々の態様がある。皮膜成分と硬化剤の
典型的な組み合わせは皮膜成分が硬化油等冷却により固
化するものであって、硬化剤が液体窒素のごとき冷媒の
場合である。Furthermore, there are various methods such as a method in which an aqueous polymer solution such as a polyacrylic acid aqueous solution is used as a film component, a flocculant such as calcium chloride as a hardening agent, and a force method in which a compound having active hydrogen is crosslinked with a crosslinking agent. A typical combination of a film component and a hardening agent is one in which the film component is hardened by cooling, such as a hardened oil, and the hardening agent is a refrigerant such as liquid nitrogen.
皮膜成分はノズルから放出されるときの粘度が500c
ps以下、好ましくは1〜30cps、特に10〜20
cpsとなるよう皮膜成分組成または温度を調整する。The film component has a viscosity of 500c when released from the nozzle.
ps or less, preferably 1 to 30 cps, especially 10 to 20 cps
Adjust the film component composition or temperature so that cps is achieved.
回転ヘッド(5)は円錐台状とするのが好ましく、その
側面に複数個、通常3〜10個の多重ノズルを設ける。The rotary head (5) is preferably in the shape of a truncated cone and is provided with multiple nozzles, usually from 3 to 10, on its sides.
回転数は1000−40000rpm程度が好ましい。The rotation speed is preferably about 1,000 to 40,000 rpm.
核成分用ノズルは直径100〜2000μmo、特に好
ましくは300〜500μ【1であり、回転へンドの回
転軸から2〜20cI◎の位置にとりつけるのが好まし
い。The nozzle for the core component has a diameter of 100 to 2000 μm, particularly preferably 300 to 500 μm, and is preferably installed at a position of 2 to 20 cI◎ from the rotation axis of the rotating hand.
皮膜成分用ノズルは核成分用ノズルの外周に同心円状に
配置する。スリット外径500〜400()μ11.特
に600〜1000μmnのスリット状開化を有するの
が適当である。The nozzle for the film component is arranged concentrically around the outer periphery of the nozzle for the core component. Slit outer diameter 500-400()μ11. In particular, it is suitable to have a slit-like opening of 600 to 1000 μm.
硬化剤用ノズルはこれを設けるときは皮膜成分用ノズル
の外周にこれと同心円状に設置する。外径1000〜8
01) 0μm1、特に1200〜60()00μmが
適当で゛ある。When provided, the curing agent nozzle is installed concentrically around the outer periphery of the film component nozzle. Outer diameter 1000~8
01) 0 μm1, especially 1200 to 60()00 μm is suitable.
本発明方法を用いると実質上核成分が皮膜成分で被覆さ
れた、2疑果していない粒径100μ川以下のマイクロ
カプセルを容易に得ることができる8By using the method of the present invention, it is possible to easily obtain microcapsules with a particle size of 100μ or less, in which the core component is substantially covered with a film component.
第1図は本発明方法を実施するための回転ヘッドの側面
図を示す。第2図は第1図回転ヘッドを下方からみた図
を示す。
(1)核成分用ノズル (2)皮膜成分用ノズル(3)
硬化剤用ノズル (4)多重ノズル(5)回転へッ)’
(6)核成分タンク(7)皮膜成分タンク (8)硬
化剤タンク(9)ハウジング(天井一部)FIG. 1 shows a side view of a rotary head for carrying out the method of the invention. FIG. 2 shows a view of the rotary head of FIG. 1 viewed from below. (1) Nozzle for core component (2) Nozzle for film component (3)
Hardening agent nozzle (4) Multiple nozzle (5) Rotating)'
(6) Core component tank (7) Film component tank (8) Hardening agent tank (9) Housing (part of ceiling)
Claims (1)
用ノズルから核成分および皮膜成分を同時に遠心力によ
って皮膜成分の硬化条件下に放出することを特徴とする
マイクロカプセルの製造法。 2、皮膜成分が加熱下に液体であり、常温で固体であり
、硬化を低温で行なう第1項記載の製造法。 3、硬化を液体窒素または液体空気で行なう第2項記載
の製造法。 4、核成分が薬液水溶液である第1項記載の製造法。 5、核成分がノズル放出時の粘度が1〜30el)sで
ある第1項記載の製造法。 6、皮+1!W T&、分のノズル放出時の粘J変が1
〜3()Cl)Sである第1項記載の製造法。 7、遠心力が1xio5−2X108dyneである第
1項記載の製造法。 8、核成分用ノズル(1)、その外周に少なくとも1ケ
のスリットを有する皮膜成分用ノズル(2)およびさら
にその外周にスリット状硬化剤用ノズル(3)からなる
多重ノズル(4)を複数個備えた回転ヘッド(5)をハ
ウクング内に備えたマイクロカプセル製造装置。 9、核成分用ノズル(1)の径が100〜2000μI
IIである第8項記載の装置。 10、皮膜成分用ノズル(2)がスリットを一個有し、
その外径が500〜2500μ輸である第8項記載の装
置。 11、硬化剤用ノズルの外征が1000〜8000μ「
nである第8項記載の装置。 12、核成分がノズルが回転ヘッドの中心から2〜20
cI11の位置に配設されている第8項記載の装置。 13、回転へ一7ドが1000−40000 rpmで
回転する第8項記載の装置。[Scope of Claims] 1. A microorganism characterized in that a core component and a film component are simultaneously discharged from a core component nozzle and a skin provided on the outer periphery of the core component nozzle under conditions for curing the film component by centrifugal force. Capsule manufacturing method. 2. The manufacturing method according to item 1, wherein the film component is liquid under heating and solid at room temperature, and curing is performed at low temperature. 3. The manufacturing method according to item 2, wherein curing is performed with liquid nitrogen or liquid air. 4. The production method according to item 1, wherein the core component is an aqueous chemical solution. 5. The manufacturing method according to item 1, wherein the core component has a viscosity of 1 to 30 el)s when discharged from a nozzle. 6. Skin +1! W T&, viscosity J change during nozzle discharge is 1
~3()Cl)S The manufacturing method according to item 1. 7. The manufacturing method according to item 1, wherein the centrifugal force is 1xio5-2X108dyne. 8. A plurality of multiple nozzles (4) consisting of a core component nozzle (1), a film component nozzle (2) having at least one slit on its outer periphery, and a slit-shaped curing agent nozzle (3) on its outer periphery. A microcapsule manufacturing device equipped with a rotary head (5) inside the houkung. 9. The diameter of the nuclear component nozzle (1) is 100 to 2000μI
9. The apparatus according to claim 8, which is II. 10. The film component nozzle (2) has one slit,
9. The device according to claim 8, wherein the outside diameter is between 500 and 2500 μm. 11. The outer diameter of the hardening agent nozzle is 1000 to 8000μ.
9. The device according to claim 8, wherein n. 12. The core component is the nozzle 2-20 mm from the center of the rotating head.
9. The device of claim 8, wherein the device is located at cI11. 13. Apparatus according to clause 8, wherein the rotating shaft rotates at 1000-40000 rpm.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2783484A JPS60172344A (en) | 1984-02-15 | 1984-02-15 | Preparation of microcapsule |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2783484A JPS60172344A (en) | 1984-02-15 | 1984-02-15 | Preparation of microcapsule |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS60172344A true JPS60172344A (en) | 1985-09-05 |
Family
ID=12231961
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2783484A Pending JPS60172344A (en) | 1984-02-15 | 1984-02-15 | Preparation of microcapsule |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60172344A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005118619A (en) * | 2003-10-14 | 2005-05-12 | Kao Corp | Manufacturing method of monodisperse solid fine particles |
-
1984
- 1984-02-15 JP JP2783484A patent/JPS60172344A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005118619A (en) * | 2003-10-14 | 2005-05-12 | Kao Corp | Manufacturing method of monodisperse solid fine particles |
JP4704672B2 (en) * | 2003-10-14 | 2011-06-15 | 花王株式会社 | Production method of monodispersed solid particles |
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