JPH01278538A - Thermoplastic resin composition - Google Patents

Thermoplastic resin composition

Info

Publication number
JPH01278538A
JPH01278538A JP10955588A JP10955588A JPH01278538A JP H01278538 A JPH01278538 A JP H01278538A JP 10955588 A JP10955588 A JP 10955588A JP 10955588 A JP10955588 A JP 10955588A JP H01278538 A JPH01278538 A JP H01278538A
Authority
JP
Japan
Prior art keywords
thermoplastic resin
resin composition
alkali metal
metal salt
formula
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
JP10955588A
Other languages
Japanese (ja)
Other versions
JP2546804B2 (en
Inventor
Yasuo Kishida
岸田 靖雄
Hitoshi Tomita
斉 冨田
Tetsuo Nishikawa
哲生 西川
Nobuo Izawa
伊沢 信雄
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.)
Kanebo Ltd
Original Assignee
Kanebo Ltd
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 Kanebo Ltd filed Critical Kanebo Ltd
Priority to JP63109555A priority Critical patent/JP2546804B2/en
Publication of JPH01278538A publication Critical patent/JPH01278538A/en
Application granted granted Critical
Publication of JP2546804B2 publication Critical patent/JP2546804B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Shielding Devices Or Components To Electric Or Magnetic Fields (AREA)
  • Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)

Abstract

PURPOSE:To obtain a thermoplastic resin composition excellent in corrosion resistance by treating the surface of a metallic filler-containing thermoplastic resin composition with a specific 3-(2-benzothiazolylthio)propionic acid (alkali metal salt). CONSTITUTION:A thermoplastic resin composition, obtained by spraying or applying a solution of one or more of 3-(2-benzothiazolylthio)propionic acid or an alkali metal salt thereof (preferably sodium salt) expressed by formula I (R is H or alkali metal) or 2-mercaptobenzothioazole expressed by formula II or an alkali metal salt thereof (preferably sodium salt) in water, an alcohol, etc., onto the surface of a thermoplastic resin composition prepared by blending 100pts.wt. thermoplastic resin (preferably polyamide resin, etc.) with preferably 50-400pts.wt. metallic filler (preferably iron, etc.) and removing the solvent, capable of maintaining good appearance for a long period without rusting and suitable as molding materials for housings, turntables, etc., of electronic and electrical appliances, etc.

Description

【発明の詳細な説明】 (産業上の利用分野) 未発明は電子・電気機器等のハウジングやターンテーブ
ル、プーリー等の成形材料として好適な優れた耐食性を
有する金属フィラー含有の熱可塑性樹脂組成物に関する
[Detailed Description of the Invention] (Industrial Application Field) A thermoplastic resin composition containing a metal filler having excellent corrosion resistance and suitable as a molding material for housings of electronic and electrical equipment, turntables, pulleys, etc. Regarding.

(従来の技術) 熱可塑性樹脂に各種形状の金属フィラーを混入して、導
電性や電磁波シールIS性をイ」与すること或いは高比
重とすることは従来より広く行なわれている。例えば特
開昭55−15274.3号公報「導電性樹脂組成物」
では、銅線やアルミ線等の繊維状導電性物質をポリエス
テル樹脂、フェノール樹脂等に配合した導電性樹脂組成
物が挙げられており、更にここでは金属粉の併用効果も
示されている。又、特開昭58−78499号公報[電
磁波ンールト用樹脂材Jには、金属繊維を熱可塑性樹脂
に均一に配合して成形する電磁波シールド用樹脂材が示
されている。更に、特開昭56−159248号公報「
熱可塑性樹脂組成物」には、ポリテトラメチレンチレフ
タレ−1・樹脂に金属粉を配合した熱可塑性樹脂組成物
が提案されている。
(Prior Art) It has been widely practiced in the past to mix metal fillers of various shapes into thermoplastic resins to impart electrical conductivity and electromagnetic wave sealing properties or to increase specific gravity. For example, JP-A-55-15274.3 ``Conductive resin composition''
cites a conductive resin composition in which a fibrous conductive material such as a copper wire or an aluminum wire is blended with a polyester resin, a phenol resin, etc., and also shows the effect of using metal powder in combination. Furthermore, Japanese Patent Application Laid-Open No. 58-78499 [Resin material for electromagnetic wave shielding J] discloses a resin material for electromagnetic wave shielding which is formed by uniformly blending metal fibers into a thermoplastic resin. Furthermore, Japanese Patent Application Laid-Open No. 56-159248 “
As the "thermoplastic resin composition", a thermoplastic resin composition in which metal powder is blended with polytetramethylene ethylene terephthalate-1 resin has been proposed.

(発明が解決しようとする問題点) 熱可塑性樹脂に金属フィラーを配合し、導電性や電磁波
シールド性等の機能性(−1与や高比重とすることば従
来より行なわれているが、金属フィラーのほとんどは耐
食性不十分で酸化され易い。その結果、導電性や電磁波
シールド性等の機能性低下や錆発生による成形品表面の
外観悪化という問題点がある。
(Problem to be solved by the invention) It has been conventional practice to blend metal fillers into thermoplastic resins to provide functionality such as conductivity and electromagnetic shielding properties (-1 or high specific gravity). Most of them have insufficient corrosion resistance and are easily oxidized.As a result, there are problems such as a decrease in functionality such as conductivity and electromagnetic shielding properties, and a deterioration in the appearance of the surface of the molded product due to rust.

この問題点を改良する方法として、ヘンヅトリアヅール
、セバシン酸塩クロム酸塩等の化学薬品による金属フィ
ラーの表面処理が行なわれているが、その防錆効果は十
分ではない。
As a method to improve this problem, surface treatment of metal fillers with chemicals such as hendstriadur, sebacate chromate, etc. has been carried out, but the rust prevention effect is not sufficient.

(問題点を解決するだめの手段) 本発明者らばかがる従来技術の有する問題点を改良すべ
く鋭意研究した結果、金属フィラーを配合した熱可塑性
樹脂組成物の表面を3−(2−ヘンジチアゾリルチオ)
プロピオン酸またはそのアルカリ金属塩で処理すれば優
れた耐食性を示すことを見出し、本発明を完成するに至
った。
(Means for Solving the Problems) As a result of intensive research aimed at improving the problems of the prior art, the present inventors found that the surface of a thermoplastic resin composition containing a metal filler was Hengethiazolylthio)
The present inventors have discovered that excellent corrosion resistance can be achieved by treatment with propionic acid or an alkali metal salt thereof, and have completed the present invention.

即ち本発明の第1は、−形成 (ただし、式中Rは、水素原子またはアルカリ金属を示
す) で表わされる化合物の少なくとも1種によって表面処理
された熱可塑性樹脂組成物であって、該組成物が金属フ
ィラーを含むことを特徴とする熱可塑性樹脂組成物であ
る。
That is, the first aspect of the present invention is a thermoplastic resin composition surface-treated with at least one compound represented by -formation (wherein R represents a hydrogen atom or an alkali metal), wherein the composition A thermoplastic resin composition characterized by containing a metal filler.

また本発明の第2は、−形成 (ただし、式中Rば、水素原子またはアルカリ金属を示
す) で表わされる化合物の少なくとも1種によって表面処理
された熱可塑性樹脂組成物であって、該組成物が金属フ
ィラーを含むことを特徴とする熱可塑性樹脂組成物であ
る。
The second aspect of the present invention is a thermoplastic resin composition surface-treated with at least one compound represented by -formation (wherein R represents a hydrogen atom or an alkali metal), A thermoplastic resin composition characterized by containing a metal filler.

以下、本発明の詳細な説明する。The present invention will be explained in detail below.

本発明に使用する一般式 (ただし、式中Rは水素原子またはアルカリ金属を示す
) で表される化合物は、3−(2−へンゾチアゾリルチオ
)プロピオン酸またはそのアルカリ金属塩であり、金属
種としては時にナトリウムが好ましい。
The compound represented by the general formula (wherein R represents a hydrogen atom or an alkali metal) used in the present invention is 3-(2-henzothiazolylthio)propionic acid or an alkali metal salt thereof. , sodium is sometimes preferred as the metal species.

3−(2−ヘンジチアゾリルチオ)プロピオン酸または
そのアルカリ金属塩を用いて熱可塑性樹脂組成物を表面
処理する際の使用量は、該組成物の表面を被覆するに十
分な量であれば特に制限されない。表面処理する方法と
しては、3−(2−ヘンジチアゾリルチオ)プロピオン
酸またはそのアルカリ金属塩を水、アルコール、グリコ
ール。
The amount used when surface treating a thermoplastic resin composition using 3-(2-hendithiazolylthio)propionic acid or its alkali metal salt is an amount sufficient to coat the surface of the composition. There are no particular restrictions. As a method for surface treatment, 3-(2-hendithiazolylthio)propionic acid or its alkali metal salt is mixed with water, alcohol, or glycol.

ケトン等の溶剤に溶解した後、熱可塑性樹脂組成物に噴
霧、或いは塗布し、次いで溶剤を除去する方法や、着色
用塗料に配合して塗布する方法等が挙げられるが、特に
制限されるものではない。
Examples include a method of dissolving it in a solvent such as ketone, spraying or coating it on a thermoplastic resin composition, and then removing the solvent, and a method of blending it into a coloring paint and applying it, but there are no particular restrictions. isn't it.

本発明に使用する一般式 (ただし、式中Rは水素原子またはアルカリ金属を示す
) で表される化合物は2−メルカプトヘンジチアゾールま
たはそのアルカリ金属塩であり、金属種としては特にナ
トリウムが好ましい。
The compound represented by the general formula (wherein R represents a hydrogen atom or an alkali metal) used in the present invention is 2-mercaptohendithiazole or an alkali metal salt thereof, and sodium is particularly preferred as the metal species.

2−メルカプトヘンジチアゾールまたはそのアルカリ金
属塩を用いて熱可塑性樹脂組成物を表面処理する際の使
用量は、該組成物の表面を被覆するに十分な量であれば
特に制限されない。表面処理する方法としては、2−メ
ルカプトヘンゾチアヅールまたはそのアルカリ金属塩を
、水、アルコール、グリコール、ゲトン等の溶剤に溶解
した後、熱可塑性樹脂組成物に噴霧、或いは塗布し、次
いで溶剤を除去する方法や、着色用塗料に配合して塗布
する方法等が挙げられるが特に制限されるものではない
The amount of 2-mercaptohendithiazole or its alkali metal salt used when surface treating a thermoplastic resin composition is not particularly limited as long as it is sufficient to coat the surface of the composition. The surface treatment method involves dissolving 2-mercaptohenzothiazur or its alkali metal salt in a solvent such as water, alcohol, glycol, getone, etc., then spraying or coating it on the thermoplastic resin composition, and then applying the solution to the thermoplastic resin composition. Examples include a method of removing it, a method of blending it into a coloring paint and applying it, but are not particularly limited.

本発明に使用する熱可塑性樹脂は、加熱による溶融流動
性を有し、射出成形加工が可能なものであれば特に制限
されないが、本発明の目的を達成する上で特に好ましい
ものとして、ポリアミド。
The thermoplastic resin used in the present invention is not particularly limited as long as it has melt flowability when heated and can be processed by injection molding, but polyamide is particularly preferred in achieving the object of the present invention.

ポリエステル、ポリオレフィン、ポリスチレン。Polyester, polyolefin, polystyrene.

ボリフエニレンオキザイド、ポリカーボネ−1・及びA
 B S樹脂が挙げられる。
Polyphenylene oxide, polycarbonate-1 and A
B S resin is mentioned.

本発明で用いられる金属フィラーとは鉄、銅。The metal fillers used in the present invention are iron and copper.

アルミニウム、亜鉛、錫、鉛等の繊維、粉末、フレーク
であって、特に好ましいものとして、鉄。
Fibers, powders, and flakes of aluminum, zinc, tin, lead, etc., with iron being particularly preferred.

銅、アルミニウムが挙げられ、またこれら鉄、銅。Copper and aluminum are mentioned, as well as these iron and copper.

アルミニウムを主成分とする合金、例えば低炭素鋼、硅
素鋼、コバルト鋼、パーマロイ、クロム鋼。
Alloys based on aluminum, such as low carbon steel, silicon steel, cobalt steel, permalloy, and chrome steel.

ステンレス鋼、マンガン鋼、モリブデン鋼、ハナジウノ
、鋼、チタニウム鋼、ニオブ−バナジウム鋼。
Stainless steel, manganese steel, molybdenum steel, titanium steel, titanium steel, niobium-vanadium steel.

黄銅、青銅等も好ましい。又、これらの金属フィラーを
2種以上併用することも出来る。
Brass, bronze, etc. are also preferred. Moreover, two or more types of these metal fillers can also be used in combination.

本発明に於4Jる金属フィラーの配合量は導電性、電磁
波シールド性、高比重等の目的とする機能や、金属フィ
ラーの種類、形状によって異なるが通常の場合、熱可塑
性樹脂100重量部に対して、金属フィラーが20〜5
00重量部、好ましくは50〜400重量部である。熱
可塑性樹脂への金属フィラーの配合は、最終的に射出成
形加工される迄の任意の段階で熱可塑性樹脂と金属フィ
ラーが均一・に混練、分散されていればよく、例えば所
定量の金属フィラーと熱可塑性樹脂とを車軸混練機或は
多軸混練機を用いて熔融混練してペレ・21・を製造し
た後、射出成形加工しても良く、又溶融混練工程を省い
て、直接混練射出成形してもよい。
The amount of the 4J metal filler in the present invention varies depending on the desired functions such as conductivity, electromagnetic shielding, and high specific gravity, as well as the type and shape of the metal filler, but in general, it is based on 100 parts by weight of the thermoplastic resin. The metal filler is 20-5
00 parts by weight, preferably 50 to 400 parts by weight. The metal filler may be blended into the thermoplastic resin as long as the thermoplastic resin and the metal filler are uniformly kneaded and dispersed at any stage up to the final injection molding process. After melt-kneading and thermoplastic resin using an axle-shaft kneader or multi-shaft kneader to produce Pelle 21, injection molding may be performed, or the melt-kneading process may be omitted and direct kneading and injection may be performed. May be molded.

本発明では他の特性を改良する目的で着色剤。In the present invention, colorants are used for the purpose of improving other properties.

滑剤2発泡剤、難燃剤、安定剤等の添加剤やガラス繊維
、炭素繊維等の補強材を(]用することも出来る。
Additives such as lubricant 2, foaming agents, flame retardants, stabilizers, and reinforcing materials such as glass fiber and carbon fiber can also be used.

以下、本発明の好適な実施態様を記す。Below, preferred embodiments of the present invention will be described.

(イ) 熱可塑性樹脂がポリアミ1−、ポリエステル。(a) Thermoplastic resin is polyamide 1-, polyester.

ポリオレフィン、ポリスチレン、ポリフエニレンオキザ
イド、ポリカーボネート及びABS樹脂であるギf許請
求の範囲第1項又は第2項記載の組成物。
The composition according to claim 1 or 2, which is a polyolefin, polystyrene, polyphenylene oxide, polycarbonate and ABS resin.

(ロ) 金属フィラーが鉄、銅、アルミニウムである特
許請求の範囲第1項又は第2項記載の組成物。
(b) The composition according to claim 1 or 2, wherein the metal filler is iron, copper, or aluminum.

(発明の効果) 本発明にかかる表面処理を施した熱可塑性樹脂組成物は
、優れた耐食性を有し、錆発生の無い良好な成形品外観
を長期に亘って維持する。
(Effects of the Invention) The thermoplastic resin composition subjected to the surface treatment according to the present invention has excellent corrosion resistance and maintains a good appearance of a molded product without occurrence of rust over a long period of time.

(実施例) 以下、実施例を用いて更に詳細な説明を行う。(Example) A more detailed explanation will be given below using examples.

実施例1 ポリブチレンテレフタレート樹脂(鐘紡■製。Example 1 Polybutylene terephthalate resin (manufactured by Kanebo ■).

PBT720)100重量部と200メソシユスクリー
ンをパスした鉄粉(川崎製鉄(株製、KIP30OA)
200重量部とを2軸混練機で溶融混練しペレットを得
た。次いで得られたベレットを使用して通常実施されて
いるポリブチレンテレフタレート樹脂の射出成形条件で
、80x150x2mmのプレー1へサンプルを成形し
た。
PBT720) 100 parts by weight and iron powder that passed a 200 mesoyu screen (Kawasaki Steel Corporation, KIP30OA)
200 parts by weight were melt-kneaded using a twin-screw kneader to obtain pellets. Then, using the obtained pellet, a sample was molded into a play 1 of 80 x 150 x 2 mm under commonly used injection molding conditions for polybutylene terephthalate resin.

このプレート・す゛ンプルに対し、3−(2−ヘンヅチ
アヅリルチオ)プロピオン酸すトリウム塩の3%アセト
ン溶液を噴霧後、100°Cの熱風乾燥機中で30分間
の加熱処理を実施しアセトンを除去した。
This plate sample was sprayed with a 3% acetone solution of thorium 3-(2-henzuthiadurylthio)propionate, and then heat-treated for 30 minutes in a hot air dryer at 100°C. Acetone was removed.

次いで1%食塩水による168時間の噴霧試験を施した
が、サンプルは優れた耐食性を示し、錆の発生も無く、
良好な外観形状を維持した。
Next, a 168-hour spray test with 1% saline solution was conducted, and the sample showed excellent corrosion resistance and no rust occurred.
Good appearance and shape were maintained.

実施例2 実施例1の3   (2−ヘンゾヂアゾリルチオ)プロ
ピオン酸すI・リウム塩に替え、3−(2−ヘンヅチア
ゾリルチオ)プロピオン酸を用いる以外は全て実施例1
と同一の工程で試験を実施した。
Example 2 Example 1-3 All the same as Example 1 except that 3-(2-henzodiazolylthio)propionic acid was used instead of (2-henzodiazolylthio)propionic acid I.lium salt.
The test was conducted using the same process.

得られたサンプルは実施例1と同等の優れた耐食性を示
し、錆の発生も無く、良好な外観形状を維持した。
The obtained sample exhibited excellent corrosion resistance equivalent to that of Example 1, did not generate rust, and maintained a good external shape.

比較例1 実施例1で得られたプレートザンプルに対し、本発明に
かかる表面処理を施さずに1%食塩水168時間の噴霧
試験を実施したが、サンプル表面全体に錆が発生した。
Comparative Example 1 The plate sample obtained in Example 1 was subjected to a 168-hour spray test with 1% saline without being subjected to the surface treatment according to the present invention, but rust was generated on the entire surface of the sample.

実施例3 6ナイロン樹脂(鐘紡側製、MC−102)100重量
部と200メノンユスクリーンをパスした鉄粉(川崎製
鉄0燭製、KIP300A)400重量部とを2軸混練
機で溶融混練しペレットを得た。次いで得られたペレッ
トを使用して、通常実施されている6ナイロン樹脂の射
出成形条件で、80X]50x2mmのプレートサンプ
ルを成形した。
Example 3 100 parts by weight of 6 nylon resin (manufactured by Kanebo Co., Ltd., MC-102) and 400 parts by weight of iron powder (manufactured by Kawasaki Steel Co., Ltd., KIP300A) that had passed a 200 menonyu screen were melt-kneaded using a twin-screw kneader. Obtained pellets. Then, using the obtained pellets, a plate sample of 80×]50×2 mm was molded under commonly used injection molding conditions for nylon 6 resin.

このプレーI・サンプルに対し、2−メルカプトヘンソ
゛チアソ゛−)レナI−リウム塩の3%アセトンン容容
器噴霧後、100°Cの熱風乾燥機で30分間の加熱処
理を施してアセトンを除去した。
This Play I sample was sprayed with 2-mercaptohenothiaso-)renalium salt in a 3% acetone container, and then heated in a hot air dryer at 100°C for 30 minutes to remove acetone. .

次いで、1%食塩水による168時間の噴霧試験を施し
たが、サンプルは優れた耐食性を示し、錆発生も認めら
れず、良好な外観形状を維持した。
Next, a 168-hour spray test with 1% saline was performed, but the sample showed excellent corrosion resistance, no rust was observed, and maintained a good appearance.

実施例4 ポリブチレンテレフタレート樹脂(鐘紡■製。Example 4 Polybutylene terephthalate resin (manufactured by Kanebo ■).

PBT720)100重量部と繊維径30μm。PBT720) 100 parts by weight and fiber diameter 30 μm.

繊維長2mmの鉄繊維((@神戸鋳鉄所製、515C)
150重量部とを2輔混練機で溶融混練しペレ7+・を
得た。次いで得られたペレットを使用して通常実施され
ているポリゾチレンテレフタレーI・樹脂の射出成形条
件で、80 x l 50 x 2 rn mのプレー
トす゛ンプルを成形した。
Iron fiber with a fiber length of 2 mm ((@Kobe Cast Iron Works, 515C)
150 parts by weight were melt-kneaded using a two-way kneader to obtain pellets 7+. Next, the obtained pellets were used to mold a plate sample of 80 x 1 x 50 x 2 rm under the usual injection molding conditions for polyzotylene terephthalate I resin.

このプレーI・サンプルに対し、2−メルヵプトヘンゾ
チアゾールの3%アセ)〜ン熔液を噴霧後、70°Cの
熱風乾燥機で30分間の加熱処理を施してアセトンを除
去した。
This Play I sample was sprayed with a 3% acetate solution of 2-mercaptohenzothiazole and then heated in a hot air dryer at 70°C for 30 minutes to remove acetone.

次いで、70 ’c、相対湿度90%の雰囲気中1.0
00時間の耐食試験を施したが、サンプルは優れた耐食
性を示し、錆発生の無い良好な外観形状を維持した。
1.0 in an atmosphere of 70'C and 90% relative humidity.
Although a 00-hour corrosion resistance test was conducted, the sample showed excellent corrosion resistance and maintained a good appearance and shape with no rust formation.

比較例2 実施例3及び4で得られたプレートリーンプルに対し、
本発明にかかる表面処理を施さずに、各々のり一ンプル
に対し、1%食塩水168時間の噴霧試験、及び70 
’C1相対湿度90%の雰囲気中1.00On、J間の
耐食試験を実施したが、−リーンプル表面全体に錆発生
が認められた。
Comparative Example 2 For the plate lean pull obtained in Examples 3 and 4,
One sample of each glue was subjected to a 168-hour spray test with 1% saline and a 70-hour spray test without surface treatment according to the present invention.
A corrosion resistance test was conducted for 1.00 On and J in an atmosphere with a relative humidity of 90%, and rust was observed on the entire -lean pull surface.

実施例、比較例より明らかなように、本発明にかかる表
面処理を施した熱可塑性樹脂組成物は優れた耐食性を示
し、電子・電気機器部品等の成形材料として好適である
As is clear from the Examples and Comparative Examples, the thermoplastic resin composition subjected to the surface treatment according to the present invention exhibits excellent corrosion resistance and is suitable as a molding material for electronic and electrical equipment parts.

Claims (2)

【特許請求の範囲】[Claims] (1)一般式 ▲数式、化学式、表等があります▼ (ただし、式中Rは、水素原子またはアル カリ金属を示す) で表わされる化合物の少なくとも1種によ って表面処理された熱可塑性樹脂組成物であって、該組
成物が金属フィラーを含むことを特徴とする熱可塑性樹
脂組成物。
(1) A thermoplastic resin composition surface-treated with at least one compound represented by the general formula ▲ Numerical formula, chemical formula, table, etc. ▼ (wherein R represents a hydrogen atom or an alkali metal) A thermoplastic resin composition, the composition comprising a metal filler.
(2)一般式 ▲数式、化学式、表等があります▼ (ただし、式中Rは水素原子またはアルカ リ金属を示す) で表わされる化合物の少なくとも1種によ って表面処理された熱可塑性樹脂組成物であって、該組
成物が金属フィラーを含むことを特徴とする熱可塑性樹
脂組成物。
(2) A thermoplastic resin composition surface-treated with at least one compound represented by the general formula ▲ Numerical formula, chemical formula, table, etc. ▼ (wherein R represents a hydrogen atom or an alkali metal) A thermoplastic resin composition characterized in that the composition contains a metal filler.
JP63109555A 1988-05-02 1988-05-02 Thermoplastic resin composition Expired - Fee Related JP2546804B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63109555A JP2546804B2 (en) 1988-05-02 1988-05-02 Thermoplastic resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63109555A JP2546804B2 (en) 1988-05-02 1988-05-02 Thermoplastic resin composition

Publications (2)

Publication Number Publication Date
JPH01278538A true JPH01278538A (en) 1989-11-08
JP2546804B2 JP2546804B2 (en) 1996-10-23

Family

ID=14513204

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63109555A Expired - Fee Related JP2546804B2 (en) 1988-05-02 1988-05-02 Thermoplastic resin composition

Country Status (1)

Country Link
JP (1) JP2546804B2 (en)

Also Published As

Publication number Publication date
JP2546804B2 (en) 1996-10-23

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