JPS6047004A - Production of organic substance powder - Google Patents
Production of organic substance powderInfo
- Publication number
- JPS6047004A JPS6047004A JP58154751A JP15475183A JPS6047004A JP S6047004 A JPS6047004 A JP S6047004A JP 58154751 A JP58154751 A JP 58154751A JP 15475183 A JP15475183 A JP 15475183A JP S6047004 A JPS6047004 A JP S6047004A
- Authority
- JP
- Japan
- Prior art keywords
- powder
- organic substance
- gas
- monomer
- carrier gas
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Landscapes
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
- Physical Vapour Deposition (AREA)
- Surface Treatment Of Glass (AREA)
- Carbon And Carbon Compounds (AREA)
- Polymerisation Methods In General (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
Abstract
Description
【発明の詳細な説明】
この発明は有機物粉体の製造方法及び壱臓物粉体の中に
別種の拐料からなる細粒を含むもの、換すすれ1J5粉
体の表面に有機物のコーティングを有する粉体g)製造
方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing an organic powder, a powder containing fine grains made of a different type of grain, and a coating of an organic substance on the surface of the 1J5 powder. Powder g) Regarding the manufacturing method.
従来、有@物V微粉体の製一方法、特に各揮■材料に広
く応用可能な微粉体の製造方法は知られていない口
また、文献によれば、ガスクロマトグラフィー充填剤の
酸素プラズマ処理による分血度の改善や、蒸発ポリエチ
レンの酸素プラズマ処理による接着性の改善等のfit
u不が知られている。しかし、粉体のコーティングの例
はほとんど知られていない。Until now, there has been no known method for producing fine powders, especially those that can be widely applied to various volatile materials.Also, according to the literature, oxygen plasma treatment of gas chromatography fillers has not been known. The fit is improved by improving the degree of blood division and adhesion by oxygen plasma treatment of evaporated polyethylene.
Ufu is known. However, few examples of powder coatings are known.
微粉体の個々の粒体表面に有限物コーティングを行なう
ことが出来れば、下記のような多くの効果が期待され、
素@υ性能の改善、11素材の開発に可能性を開くもの
となる。If it is possible to apply a finite substance coating to the surface of each particle of fine powder, many effects such as those listed below can be expected.
This will open up possibilities for improving the performance of the element @υ and developing 11 materials.
この発明は、プラズマ重合法金利月Jし、プラズマ空I
ll中で生ずる風合反応によシ有臓物の微粉体を得、或
いは粉体粒子六面に有−物のコーディングを竹う新規な
方法を提供しようとするものである。This invention is based on the plasma polymerization process and the plasma polymerization process.
The present invention aims to provide a new method for obtaining fine powder of organoleptics by the texture reaction that occurs in the molten metal, or for coating six sides of the powder particles with organoleptics.
@1図はこの発明を実施する反応装置の1例を示す。高
周波コイル2を有する反応しlの上部に粉体導入口3に
、設り、コーティングナベき粉体はArそV曲のキャリ
アカス導入D 4からのガスと共に反応器1中に導入さ
れる。放電コイル2の下流に1種または複数種のモノマ
ーガスの力・入口5を設ける。6Nコーテイングされた
粉体を集収する粉体トラップであり、7は排気口である
。Figure @1 shows an example of a reactor for carrying out this invention. A powder inlet port 3 is installed in the upper part of the reactor 1 having a high frequency coil 2, and the coated powder is introduced into the reactor 1 together with the gas from the carrier cass introduction D4 of the Arson V track. A power inlet 5 for one or more monomer gases is provided downstream of the discharge coil 2 . This is a powder trap that collects the 6N coated powder, and 7 is an exhaust port.
尋人1」4からのキャリアが中に浮遊した状糾で流下す
る粉体は、尚周波コイル2によるプラズマ中をlIn過
する間に、このグラズマ領域の′F都に導入され、活性
化されたモノマーが、その六面で止6合することによシ
完全にコーティングされる。The powder flowing down with carriers suspended in it from Hirojin 1'4 is introduced into the 'F' region of this glazma region and activated while passing through the plasma caused by the high frequency coil 2. The monomers are completely coated by bonding on their six faces.
コーティングの膜厚制両は粉体の落下速度を制御して行
なうのが便イ・口であり、ガス導入Ll 4からのキャ
リアカスの冑1人情及び排気厳υ制陣によって7丁なう
ことが出来る。ξのf出、キャリアガスQ流れの方向の
変更やレーザーによる粉体のr′f−揚等によっても落
下速度の制菌は可能である。It is convenient to control the thickness of the coating by controlling the falling speed of the powder, and it is possible to control the thickness of the carrier sludge from the gas introduction Ll 4 and strictly control the exhaust. I can do it. It is also possible to control the falling velocity by changing the flow direction of the carrier gas Q, r'f-lifting the powder by a laser, etc.
有1〃物コーティングによって、粉体り、相互にまたは
反【己器壁に付着し易くなるが、これケ防ぐには、反応
器を昇温してコーテイング膜の架橋の増加、低分子量分
子の除去、器壁からの再放出t ’i’iなわぜ゛るの
がよい。Chemical coatings tend to cause particles to stick to each other or to the walls of the reactor, but to prevent this, the temperature of the reactor can be increased to increase cross-linking of the coating film and reduce the amount of low-molecular-weight molecules. It is best to remove it and re-release it from the vessel wall.
1k、モノマーのプラズマ重合を、粉体吹口で行なわせ
るだけでなく、粉体を導入しないノ。1k, not only the plasma polymerization of monomer is carried out through a powder blowing hole, but also no powder is introduced.
ラズマ空…」で行々わぜることによシ、有1女1勿・有
機シリコ゛ン々I■微粉体を得ることが出来る。By performing the process using a lasma, it is possible to obtain a fine powder of organic silicon.
このように17で得られた微粉体tJS架橋りまた粉体
であるたヤ)、mil !?’l性粉体として利用出来
る。In this way, the fine powder obtained in step 17 is a cross-linked powder (tJS), mil! ? It can be used as a lactic powder.
兵空中熱分額によって超微粉秋活性脚の生成が可能であ
る等の利用ができる。It can be used to generate ultra-fine powder fall active legs using the amount of heat in the air.
す、下実施例を示す。An example is shown below.
l)スチレン粉状物の合成と炭化物粉体1tu度v 5
1′−行千板電極を有する゛円筒反応容トな用い、0.
3tOrr υ圧力のアルゴンースグーレン晶自′カス
に、13.5 MB2.50Wυ高周波を印加l/てプ
ラズマを生じさせることにより、粉体が合成された。l) Synthesis of styrene powder and carbide powder 1tu degree v 5
1' - Use of a cylindrical reaction vessel with rows of electrodes, 0.
A powder was synthesized by generating plasma by applying a 13.5 MB 2.50 W υ radio frequency to the argon-sgoolene crystal autoscum at a pressure of 3 tOrr υ.
この粉体は約50?+g/c−の密度を有し、大気IE
!7)Arガス中で500℃に加熱することによシ、溶
解することなく炭化し、炭化物粉体を得た。This powder is about 50? +g/c- density, atmospheric IE
! 7) By heating to 500° C. in Ar gas, the mixture was carbonized without dissolving to obtain carbide powder.
2)カラスベレントのコーチインク
集施向1と(1りじ反応、器を用い直径200〜300
μmのガラスペレントにコーティング葡1]い、一様な
膜厚のコーティングを得た。2) Coat ink collection of crow berent 1 and
A coating of uniform thickness was obtained by coating a glass pellet with a diameter of 1 µm.
モノマーとしてり、スチレン、エタン、テトラメチル錫
、テトラメチルシラン等が叱用可能であったC
3)金&16コーテイング1−シたガラスベレントのコ
ーチインク
笑施向2と同様の装板方法により、At、AU。As a monomer, styrene, ethane, tetramethyltin, tetramethylsilane, etc. can be used. , A.U.
AL ’75で缶軸うコープインクし71cガラスペレ
ツトを一様な膜厚で自に1bコーテイングした。I coated 71c glass pellets with a uniform thickness of 1b using AL'75 coat ink.
この発明は、上記のようにモノマーガスをフラスマ領域
甲に尋人し、空間に浮遊したままの状紗で框Bさぜるの
で、番んに微粉体が得られる上、金帆、無除物、有除物
等υ各抽拐科の粉体を、上記服822間を超過させるこ
とによシ、膜#−v均一な、有−物のコーティング層を
極めてI′Fr111iに形成しうるものである。In this invention, as described above, monomer gas is introduced into the flask area A and mixed with the gauze while suspended in the space, so that fine powder can be obtained in no time. By passing the powder of each extractive species, such as substances and foreign matter υ, over the space between the layers 822, a uniform coating layer of substances can be formed on the film #-v, which is extremely I'Fr111i. It is something.
図面Uこの発明の方法に用いられる反応装置の1例を示
す如、急回である。
に反応器 2:高周波コイル 3:粉体導入口 4:キ
ャリアガス導入口 5:モノマー導入口 6:粉体トラ
ップ 7:排気口特詐出願人 新技術開発事柴団Drawing U shows an example of a reaction apparatus used in the method of this invention, and is a rapid turnaround. Reactor 2: High frequency coil 3: Powder inlet 4: Carrier gas inlet 5: Monomer inlet 6: Powder trap 7: Exhaust port
Claims (1)
領域にモノマーガスを導入し、該領域近傍空間でプラズ
マ重合を行なわせることを%微とする有機物粉体の製造
方法 2)′に空槽中に一事・いて、キャリアカスの高周波プ
ラズマ領域にモノマーガスを導入すると共に、粉体粒子
を該領域を曲過させ、該粉体粒子の表面にプラズマ重合
によシ均一なコーテイング膜を形成させることを特黴左
する有機物によシコーティングされた粉体の製造方法[Claims] 1) Method 2 for producing organic powder, which comprises introducing a monomer gas into a colasian plasma region of a carrier cassette in a vacuum chamber, and causing plasma polymerization to occur in a space near the region. )', a monomer gas is introduced into the high-frequency plasma region of the carrier scum, the powder particles are bent through this region, and the surface of the powder particles is uniformly coated by plasma polymerization. Method for producing powder coated with an organic substance that has a special feature of forming a coating film
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58154751A JPS6047004A (en) | 1983-08-26 | 1983-08-26 | Production of organic substance powder |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58154751A JPS6047004A (en) | 1983-08-26 | 1983-08-26 | Production of organic substance powder |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6047004A true JPS6047004A (en) | 1985-03-14 |
JPH0460123B2 JPH0460123B2 (en) | 1992-09-25 |
Family
ID=15591110
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58154751A Granted JPS6047004A (en) | 1983-08-26 | 1983-08-26 | Production of organic substance powder |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6047004A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2252559A (en) * | 1991-02-09 | 1992-08-12 | Tioxide Group Services Ltd | Method of coating inorganic particles |
US5281696A (en) * | 1992-12-07 | 1994-01-25 | Shell Oil Company | Removal of hydrogenation catalyst from polymer solutions by trialkyl aluminum precipitation |
WO2007028798A1 (en) * | 2005-09-05 | 2007-03-15 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Method for producing a metal powder and an electrically insulating polymer composite material, polymer composite material and electronic device |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58100601A (en) * | 1981-12-09 | 1983-06-15 | Japan Synthetic Rubber Co Ltd | Coated ultrafine particle or its film and method and device for forming said particle or film |
-
1983
- 1983-08-26 JP JP58154751A patent/JPS6047004A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58100601A (en) * | 1981-12-09 | 1983-06-15 | Japan Synthetic Rubber Co Ltd | Coated ultrafine particle or its film and method and device for forming said particle or film |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2252559A (en) * | 1991-02-09 | 1992-08-12 | Tioxide Group Services Ltd | Method of coating inorganic particles |
GB2252559B (en) * | 1991-02-09 | 1994-10-12 | Tioxide Group Services Ltd | Coating process |
US5281696A (en) * | 1992-12-07 | 1994-01-25 | Shell Oil Company | Removal of hydrogenation catalyst from polymer solutions by trialkyl aluminum precipitation |
WO2007028798A1 (en) * | 2005-09-05 | 2007-03-15 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Method for producing a metal powder and an electrically insulating polymer composite material, polymer composite material and electronic device |
Also Published As
Publication number | Publication date |
---|---|
JPH0460123B2 (en) | 1992-09-25 |
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