JPS62149727A - Composite plastic particle and its production - Google Patents

Composite plastic particle and its production

Info

Publication number
JPS62149727A
JPS62149727A JP29661085A JP29661085A JPS62149727A JP S62149727 A JPS62149727 A JP S62149727A JP 29661085 A JP29661085 A JP 29661085A JP 29661085 A JP29661085 A JP 29661085A JP S62149727 A JPS62149727 A JP S62149727A
Authority
JP
Japan
Prior art keywords
particles
plastic
metal
composite
particle size
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
JP29661085A
Other languages
Japanese (ja)
Inventor
Masumi Koishi
真純 小石
Makoto Hiyamizu
冷水 真
Katsunori Iwatani
岩谷 勝能
Yasushi Abe
靖 阿部
Hiroyuki Sasaki
佐々木 弘行
Hideaki Shibuya
渋谷 英昭
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.)
Tokyo Tekko Co Ltd
Nikko Rica Corp
Original Assignee
Tokyo Tekko Co Ltd
Nikko Rica Corp
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 Tokyo Tekko Co Ltd, Nikko Rica Corp filed Critical Tokyo Tekko Co Ltd
Priority to JP29661085A priority Critical patent/JPS62149727A/en
Publication of JPS62149727A publication Critical patent/JPS62149727A/en
Pending legal-status Critical Current

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  • Processes Of Treating Macromolecular Substances (AREA)

Abstract

PURPOSE:To obtain the titled particles excellent in heat resistance, by coating the surfaces of plastic particles with fine particles of a simple substance, alloy or compound of a (semi-)metal. CONSTITUTION:Plastic particles (A) (e.g., ethylene/vinyl acetate copolymer particles) are mixed with 0.1-50wt% ultrafine particles (B) selected from among a simple substance of a metal (e.g., Ni) or of a semi-metal (e.g., silicon), an alloy of a (semi-)metal (e.g., Fe/Ni alloy) or its compound such as an oxide (e.g., TiO), nitride (e.g., Si3N4) and carbide (e.g., WC), each of which has a particle diameter of 1mum or below, preferably, of 0.01-1mum and is 1/10-1/100 of that of component A to form a composite layer of component B uniformly adhered and the fixed to the surface of component A. If desired, this procedure is repeated to form composite particles of an at least bilayer structure.

Description

【発明の詳細な説明】 (産業上の利用分野) この発明は、各種プラスチックの機能を向上し、その用
途の拡大を図るプラスチック複合化粒子、及びその製造
法に係わるものである。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to plastic composite particles that improve the functions of various plastics and expand their uses, and a method for producing the same.

(従来技術とその問題点) 従来のプラスチック粒子においては、これを例えばセラ
ミック粉体との混合物として溶射すると、プラスチック
とセラミックとがその粒子の差によって分離偏在し易く
、そのために均一な塗膜が得られ難いという問題があっ
た。
(Prior art and its problems) When conventional plastic particles are thermally sprayed as a mixture with ceramic powder, for example, the plastic and ceramic tend to be separated and unevenly distributed due to the difference in the particles, which makes it difficult to obtain a uniform coating film. The problem was that it was difficult to obtain.

(問題点を解決するための手段) この発明は、プラスチック粒子の表面をセラミックの超
微粒子で被覆したプラスチックの複合化粒子にすれば上
記の問題点を解決出来るばかりでなく、セラミックに代
えて他の素材の超微粒子を同様にプラスチックの粒子面
に適用すればプラスチックに新たな特性を付加し、その
機能が向上できることを見出したものである。
(Means for Solving the Problems) This invention not only solves the above problems by making plastic composite particles whose surfaces are coated with ultrafine ceramic particles, but also uses other materials instead of ceramics. It was discovered that if ultrafine particles of this material were similarly applied to the particle surface of plastic, new properties could be added to the plastic and its functions could be improved.

従って、この発明の目的は、プラスチック粒子の表面を
改質することにより、これまでのプラスチックの特性を
変化させ、その機能を改善し、従来の利用分野における
各種問題点を解決すると共に、新たな用途の拡大を図る
にある。
Therefore, the purpose of this invention is to change the properties of conventional plastics by modifying the surface of plastic particles, improve their functions, solve various problems in conventional fields of use, and create new The aim is to expand its uses.

(発明の構成) 次に、この発明の詳細について説明する。(Structure of the invention) Next, details of this invention will be explained.

先ず、この発明において出発原料として用いられるプラ
スチック粒子は、例えばポリエチレン。
First, the plastic particles used as a starting material in this invention are, for example, polyethylene.

ポリプロピレン、エチレン・酢酸ビニル共重合体、ポリ
塩化ビニル、ポリスチレン、ポリエチレンテレフタレー
1−、ポリアミド、メタクリル樹脂等の熱可塑性樹脂、
また、エポキシ、フェノール、ポリウレタン、メラミン
樹脂等の熱硬化性樹脂の単独または2種以上の混合物の
粒子が挙げられる。
Thermoplastic resins such as polypropylene, ethylene/vinyl acetate copolymer, polyvinyl chloride, polystyrene, polyethylene terephthalate, polyamide, methacrylic resin,
Further, examples include particles of thermosetting resins such as epoxy, phenol, polyurethane, and melamine resin alone or in a mixture of two or more thereof.

他方、これらのプラスチック粒子の表面に層状に被覆さ
れる超微粒子は粒径が1μm以下、好ましくは0.01
〜1μmのものであって、プラスチック粒子の粒径の1
/10〜1/100であることが望ましく、その素材と
しては鉄、コバルト、ニッケル、パラジウム、白金、ク
ロム、モリブデン、チタン、ジルコニウム、銅、亜鉛、
アルミニウム、銀、マンガン等の金属およびシリコン、
はう素等の半金属の単体類、また鉄/ニッケル、銀/パ
ラジウム、コバルト/クロム合金等これらの金属・半金
属の合金類、さらに酸化チタン、酸化けい素、酸化アル
ミニウム、酸化ジルコニウム等の酸化物。
On the other hand, the ultrafine particles coated in a layer on the surface of these plastic particles have a particle size of 1 μm or less, preferably 0.01 μm or less.
~1 μm, which is 1 μm of the particle size of plastic particles.
/10 to 1/100 is desirable, and the materials include iron, cobalt, nickel, palladium, platinum, chromium, molybdenum, titanium, zirconium, copper, zinc,
metals such as aluminum, silver, manganese, and silicon;
Single metalloids such as boron, alloys of these metals and semimetals such as iron/nickel, silver/palladium, and cobalt/chromium alloys, as well as titanium oxide, silicon oxide, aluminum oxide, zirconium oxide, etc. oxide.

窒化チタン、窒化けい素、窒化ジルコニウム等の窒化物
、炭化けい素、炭化タングステン、炭化チタン等の炭化
物等が挙げられる。これらは単独または2種以上の混合
物として使用される。
Examples include nitrides such as titanium nitride, silicon nitride, and zirconium nitride, and carbides such as silicon carbide, tungsten carbide, and titanium carbide. These may be used alone or as a mixture of two or more.

この複合化粒子の形状は前述のプラスチック粒子に、こ
れらの超微粒子を、好ましくは0.1〜50%の重量割
合で、単に混合することによって達成される。この際前
述した超微粒子は表面活性が極めて大きいため、混合に
際して発生する摩擦帯電、摩擦熱が引き金となって、プ
ラスチック粒子の表面に均一に、また強固に付着、固定
されて複合層を形成する。
This composite particle shape is achieved by simply mixing these ultrafine particles with the aforementioned plastic particles, preferably in a weight proportion of 0.1 to 50%. At this time, the ultrafine particles mentioned above have extremely high surface activity, so the frictional electrification and frictional heat generated during mixing act as triggers, and they are uniformly and firmly attached and fixed to the surface of the plastic particles, forming a composite layer. .

この表面被覆層の形成は、必要に応じ、この操作を反覆
すれば2層以上の多層構造の複合化粒子にすることがで
きる。
This surface coating layer can be formed into composite particles having a multilayer structure of two or more layers by repeating this operation as necessary.

実施例l 5P−500(東し社製、ナイロン12)の真球状粉末
(平均粒径5μm)100重量部に対し。
Example 1 Based on 100 parts by weight of true spherical powder (average particle size 5 μm) of 5P-500 (manufactured by Toshisha Co., Ltd., nylon 12).

窒化チタンの超微粒子(東京鐵鋼製、平均粒径0.05
μm)20重量部を加えボールミル中で6時間混合調製
した。処理前プラスチック粒子と得られた複合化粒子の
物性を測定した結果を第1表に、また両者の電子顕微鏡
写真を第1図に示す。
Ultrafine particles of titanium nitride (manufactured by Tokyo Steel, average particle size 0.05
20 parts by weight (μm) were added and mixed for 6 hours in a ball mill. The results of measuring the physical properties of the plastic particles before treatment and the composite particles obtained are shown in Table 1, and electron micrographs of both are shown in FIG.

第   1   表 処理前後の試料各1gを水10cc中に加え攪拌後静置
したところ、処理前の試料では水と分離して浮上したが
、処理後の試料では水に一様に分散した。
Table 1: When 1 g each of the samples before and after treatment was added to 10 cc of water, stirred, and left to stand, the samples before treatment separated from the water and floated to the surface, but the samples after treatment were uniformly dispersed in the water.

実施例2 エチレン・酢ビ共重合体(バイエル社製)の粉末(平均
粒径150μm)100重量部に対し。
Example 2 Based on 100 parts by weight of powder (average particle size 150 μm) of ethylene/vinyl acetate copolymer (manufactured by Bayer AG).

炭化けい素の超微粒子(東京鐵鋼製、平均粒径0.08
μm)2.5重量部を加えボールミル中で2時間混合調
製した。
Ultrafine silicon carbide particles (manufactured by Tokyo Steel, average particle size 0.08
2.5 parts by weight (μm) was added and mixed for 2 hours in a ball mill.

粒径100〜200μmのエチレン酢ビ共重合体(EV
A)の粉体と炭化けい素の粉末の混合物を、プラスチッ
ク粉体用ガス炎溶射装置を用いて鉄板上に溶射したとこ
ろ、溶射ノズルの詰りか発生して作業性が悪く、またE
VAの粉末と、炭化けい素の粉末とが分離偏在して均一
な塗膜が得られなかった。しかし、上記の方法によって
得られたエチレン酢ビ共重合体の炭化けい素による複合
粒子を用いて溶射したところ、溶射時の作業性に何等の
支障が無く、また均一で平滑な複合塗膜が得られた。
Ethylene vinyl acetate copolymer (EV
When a mixture of powder A) and silicon carbide powder was sprayed onto a steel plate using a gas flame spraying device for plastic powder, the spray nozzle was clogged, resulting in poor workability.
VA powder and silicon carbide powder were separated and unevenly distributed, making it impossible to obtain a uniform coating film. However, when thermal spraying was performed using silicon carbide composite particles of ethylene vinyl acetate copolymer obtained by the above method, there was no problem with workability during thermal spraying, and a uniform and smooth composite coating was obtained. Obtained.

実施例3 ポリエチレンの粉末(平均粒径100μm)100重量
部にニッケル金属の超微粒子(平均粒径0.07μm)
10重量部を加えて実施例1と同様の方法で混合調製し
た。
Example 3 Ultrafine nickel metal particles (average particle size 0.07 μm) were added to 100 parts by weight of polyethylene powder (average particle size 100 μm).
A mixture was prepared in the same manner as in Example 1 by adding 10 parts by weight.

処理後の試料は処理前のものに比べ分散性、親水性が向
上した。
The sample after treatment had improved dispersibility and hydrophilicity compared to the sample before treatment.

実施例4 ポリエチレンテレフタレートの粉末(平均粒径1八、、
、jiハ八へ−1;1.蔗を一四i>キカζ)の情漁f
atヱ(平均粒径0.05μm)10重量部を加え、実
施例1と同様の方法で混合調製した。
Example 4 Polyethylene terephthalate powder (average particle size 18,
, jihahaha-1;1. 14 i > kika ζ)
10 parts by weight of ate (average particle size 0.05 μm) were added and mixed and prepared in the same manner as in Example 1.

処理後の試料は処理前のものに比べ分散性、親水性が向
上していることが判った。
It was found that the sample after treatment had improved dispersibility and hydrophilicity compared to the sample before treatment.

実施例5 ナイロンの粉末(平均粒径5μm)100重量部に、融
点232°Cの低融点金属(金属名錫)の超微粒子(平
均粒径0.1μm) 5重量部を加えて実施例1と同様
の方法で混合調製して複合化粒子を得た。これに更にセ
ラミックス超微粒子(化合物名炭化けい素、平均粒径0
.05μm)を5重量%加えて同様に混合調製し複合化
された金属質マイクロカプセルを得た、このものは、分
散性が優れてていることが判った。
Example 5 Example 1 was prepared by adding 5 parts by weight of ultrafine particles (average particle size 0.1 μm) of a low melting point metal (metal name: tin) with a melting point of 232°C to 100 parts by weight of nylon powder (average particle size 5 μm). Composite particles were obtained by mixing and preparing in the same manner as above. In addition, ceramic ultrafine particles (compound name: silicon carbide, average particle size 0)
.. 05 μm) was added and mixed in the same manner to obtain composite metallic microcapsules, which were found to have excellent dispersibility.

(発明の効果) 以上の如く、この発明の複合化粒子は、出発原料のプラ
スチック粒子の種類と被覆用の超微粒子の素材の種類と
を適宜選択することにより、出発原料であるプラスチッ
ク粒子の耐熱性、耐摩耗性、または耐候性を向上させる
(Effects of the Invention) As described above, the composite particles of the present invention can be produced by appropriately selecting the type of plastic particles as the starting raw material and the type of material for the coating ultrafine particles. improve durability, abrasion resistance, or weather resistance.

プラスチック粒子に接着性、親水性または特殊機能を付
与する、超微粒子のハンドリング性を向上させる等の効
果を奏するので、溶射材料、顔料、塗料、各種プラスチ
ック成形材料、医薬用結合剤、触媒担体、磁性材料等の
用途分野において広く利用することができる。
It has the effect of imparting adhesiveness, hydrophilicity, or special functions to plastic particles, and improving the handling of ultrafine particles, so it is useful for thermal spraying materials, pigments, paints, various plastic molding materials, pharmaceutical binders, catalyst carriers, It can be widely used in fields of application such as magnetic materials.

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

第1図(a、b)はナイロン12の粉末に窒化チタンの
超微粒子を処理し複合化した際の、処理前後の粒子の状
態を示す電子顕微鏡写真である。
FIGS. 1(a, b) are electron micrographs showing the state of particles before and after treatment when nylon 12 powder is treated with ultrafine particles of titanium nitride to form a composite.

Claims (1)

【特許請求の範囲】 1)プラスチック粒子の表面を、粒子径1μm以下の1
種または2種以上の金属または半金属の単体、合金もし
くは化合物の超微粒子で、1層または2層以上被覆して
成るプラスチック複合化粒子。 2)プラスチック粒子に、粒子径1μm以下の1種また
は2種以上の金属または半金属の単体、合金もしくは化
合物の超微粒子を混合することにより、プラスチック粒
子の表面に超微粒子をその表面活性により層状に付着固
定させ、更に必要に応じこれを反覆することを特徴とす
るプラスチック複合化粒子の製造方法。
[Claims] 1) The surface of the plastic particles is coated with 1 μm or less in particle size.
Plastic composite particles coated with one or more layers of ultrafine particles of a single metal, alloy, or compound of two or more metals or semimetals. 2) By mixing ultrafine particles of one or more metals or semimetals, alloys, or compounds with a particle size of 1 μm or less into plastic particles, the ultrafine particles can be layered on the surface of the plastic particles by their surface activity. 1. A method for producing composite plastic particles, which comprises adhering and fixing the particles to a plastic composite particle, and repeating this process as necessary.
JP29661085A 1985-12-24 1985-12-24 Composite plastic particle and its production Pending JPS62149727A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP29661085A JPS62149727A (en) 1985-12-24 1985-12-24 Composite plastic particle and its production

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP29661085A JPS62149727A (en) 1985-12-24 1985-12-24 Composite plastic particle and its production

Publications (1)

Publication Number Publication Date
JPS62149727A true JPS62149727A (en) 1987-07-03

Family

ID=17835783

Family Applications (1)

Application Number Title Priority Date Filing Date
JP29661085A Pending JPS62149727A (en) 1985-12-24 1985-12-24 Composite plastic particle and its production

Country Status (1)

Country Link
JP (1) JPS62149727A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008013266A1 (en) * 2006-07-28 2008-01-31 Kyodo Printing Co., Ltd. Resin particle with powder united thereto and method of forming the same, particle-containing molded object, particle-containing sheet material, and method of forming these, and functional sheet and process for producing functional sheet
JP2008050592A (en) * 2006-07-28 2008-03-06 Kyodo Printing Co Ltd Resin particle with powder united thereto and method for granulating the same, particle-containing molded article, particle-containing sheet material, and method of forming these

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008013266A1 (en) * 2006-07-28 2008-01-31 Kyodo Printing Co., Ltd. Resin particle with powder united thereto and method of forming the same, particle-containing molded object, particle-containing sheet material, and method of forming these, and functional sheet and process for producing functional sheet
JP2008050592A (en) * 2006-07-28 2008-03-06 Kyodo Printing Co Ltd Resin particle with powder united thereto and method for granulating the same, particle-containing molded article, particle-containing sheet material, and method of forming these

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