[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

JPH08157715A - Flame-retardant resin composition - Google Patents

Flame-retardant resin composition

Info

Publication number
JPH08157715A
JPH08157715A JP33102894A JP33102894A JPH08157715A JP H08157715 A JPH08157715 A JP H08157715A JP 33102894 A JP33102894 A JP 33102894A JP 33102894 A JP33102894 A JP 33102894A JP H08157715 A JPH08157715 A JP H08157715A
Authority
JP
Japan
Prior art keywords
weight
resin composition
nylon
thermoplastic resin
acid compound
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
JP33102894A
Other languages
Japanese (ja)
Other versions
JP3261274B2 (en
Inventor
Tetsuo Nishikawa
哲生 西川
Hitoshi Tomita
斉 冨田
Kazuo Haruta
和夫 春田
Katsumi Onishi
克己 大西
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 JP33102894A priority Critical patent/JP3261274B2/en
Publication of JPH08157715A publication Critical patent/JPH08157715A/en
Application granted granted Critical
Publication of JP3261274B2 publication Critical patent/JP3261274B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE: To obtain a high-specific-gravity thermoplastic resin composition having good moldability and capable of giving a molding having excellent mechanical strengths, good surface appearance and an excellent degree of surface blackness. CONSTITUTION: This resin composition is prepared by adding 0.01-0.5 pt.wt. saturated aliphatic carboxylic acid compound represented by the formula: [CH3 (CH2 )mCOO]nR (wherein (m) is an integer of 14-26, (n) is 1 or 2; and R is an alkali metal, an alkaline earth metal, hydrogen or an aliphatic hydrocarbon group) to 100 pts.wt. composition comprising nylon 6 having a relative viscosity of 2.1-3.0, 40-70wt.% stainless steel powder of a mean particle diameter of 3-25μm, 5-15wt.% glass fiber and 0.3-2.0wt.% carbon black.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、機械的強度に優れ、成
形性及び成形品表面外観が良好であり、成形品表面の黒
色度が優れた高比重熱可塑性樹脂組成物に関するもので
ある。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a high specific gravity thermoplastic resin composition having excellent mechanical strength, excellent moldability and surface appearance of a molded product, and excellent blackness of the surface of the molded product.

【0002】[0002]

【従来の技術】6ナイロンを初めとする熱可塑性樹脂
は、金属材料に比べて加工が容易で耐蝕性に優れ、かつ
軽量である上に比較的安価なことから、近年機械部品、
精密部品、一般工業部品、日用雑貨などの素材や、構造
材料など多くの分野において幅広く用いられている。
2. Description of the Related Art Thermoplastic resins such as 6-nylon are easy to process, have excellent corrosion resistance, are lightweight, and are relatively inexpensive as compared with metal materials.
It is widely used in many fields such as materials for precision parts, general industrial parts, daily sundries, and structural materials.

【0003】更に金属材料に比べ、製品の生産性に優れ
ており、特に射出成形法を採用した場合に顕著であり、
複雑形状の成形品が一工程で成形できることが高成長を
遂げた理由の一つである。
Further, it is superior in productivity to products as compared with metallic materials, and particularly when the injection molding method is adopted,
One of the reasons for achieving high growth is that molded products with complicated shapes can be molded in a single process.

【0004】しかしながら、用途によっては金属並みの
重量感を必要とする場合があり、通常の熱可塑性樹脂で
は対応できなかった。
However, depending on the application, there is a case where a weight feeling similar to that of a metal is required, and an ordinary thermoplastic resin cannot handle it.

【0005】そこで近年、熱可塑性樹脂に金属粉を溶融
混練等で混合した材料が開発された(特開昭61−20
0165号公報)。
Therefore, in recent years, a material has been developed in which a metal powder is mixed with a thermoplastic resin by melt-kneading or the like (JP-A-61-20).
No. 0165).

【0006】この材料の場合、熱可塑性樹脂使用時の生
産性を維持し、かつ重量感もあるが、形成品の表面色は
灰色を呈する。
[0006] In the case of this material, productivity is maintained when a thermoplastic resin is used, and there is a feeling of weight, but the surface color of the formed product is gray.

【0007】一方、金属材料のうち最も幅広く使われて
いる鉄は、自然に黒錆に覆われ独特の黒色を呈するた
め、金属粉を複合した熱可塑性樹脂は鉄代替としては色
調面で不満足である。
On the other hand, iron, which is the most widely used metal material, is naturally covered with black rust and exhibits a unique black color. Therefore, a thermoplastic resin containing metal powder is unsatisfactory in terms of color tone as an alternative to iron. is there.

【0008】このため、塗装を施すことが行われるが、
工程増加の問題がある。
For this reason, painting is performed, but
There is a problem of increased processes.

【0009】[0009]

【発明が解決しようとする課題】本発明の目的とすると
ころは、上記従来技術の問題点を解決し、機械的強度に
優れ、成形性及び成形品表面外観が良好であり、成形品
表面の黒色度に優れた重量感のある熱可塑性樹脂組成物
を提供するにある。
The object of the present invention is to solve the above-mentioned problems of the prior art, to provide excellent mechanical strength, good moldability and good appearance of the surface of a molded product, and Another object of the present invention is to provide a thermoplastic resin composition having an excellent blackness and a heavy feeling.

【0010】[0010]

【課題を解決するための手段】上述の目的は、(A)相
対粘度 2.1〜3.0の6ナイロン,(B)平均粒子
径 3〜25μmのステンレス粉末40〜70重量%,
(C)ガラス繊維5〜15重量%,(D)カーボンブラ
ック 0.3〜2.0重量%,からなる組成物100重
量部に対して、(E)下記一般式(I)で示される飽和
脂肪族カルボン酸化合物0.01〜0.5重量部を配合
してなることを特徴とする熱可塑性樹脂組成物によって
達成される。 〔CH3 (CH2 )m COO〕n R・・・・・(I) (式中mは14〜26の整数、nは1または2、Rはア
ルカリ金属、アルカリ土類金属、水素あるいは脂肪族炭
化水素基を表す。)
The above-mentioned objects are as follows: (A) 6 nylon having a relative viscosity of 2.1 to 3.0, (B) 40 to 70% by weight of stainless powder having an average particle diameter of 3 to 25 μm,
(C) 5 to 15% by weight of glass fiber, (D) 0.3 to 2.0% by weight of carbon black, to 100 parts by weight of a composition, (E) saturation represented by the following general formula (I) This is achieved by a thermoplastic resin composition characterized by containing 0.01 to 0.5 part by weight of an aliphatic carboxylic acid compound. [CH 3 (CH 2) m COO] n R ····· (I) (an integer wherein m is 14 to 26, n is 1 or 2, R is an alkali metal, alkaline earth metal, hydrogen or fats Represents a group hydrocarbon group.)

【0011】以下、本発明を詳細に説明する。本発明に
用いる6ナイロンは、ε−カプロラクタムを重合させる
ことにより得られる線状ポリマーを意味するが、6ナイ
ロンの基本的性質を損なわない範囲において、ε−カプ
ロラクタム以外のモノマーが共重合ないしブレンドされ
ていても構わない。
The present invention will be described in detail below. The 6-nylon used in the present invention means a linear polymer obtained by polymerizing ε-caprolactam, but monomers other than ε-caprolactam are copolymerized or blended within a range not impairing the basic properties of 6-nylon. It doesn't matter.

【0012】本発明に用いる(A)6ナイロンは、JI
S K 6810法で測定した相対粘度が2.1〜3.
0であることが肝要である。
The (A) 6 nylon used in the present invention is JI
The relative viscosity measured by the SK 6810 method is 2.1 to 3.
It is essential that it is 0.

【0013】相対粘度が2.1未満の場合、機械強度が
不良となり、相対粘度が3.0を超える場合、成形性が
不良となる。
If the relative viscosity is less than 2.1, the mechanical strength will be poor, and if the relative viscosity is more than 3.0, the moldability will be poor.

【0014】本発明に用いる(B)ステンレス粉末の平
均粒子径は3〜25μmであることが肝要である。好ま
しくは3〜20μmである。
It is important that the (B) stainless powder used in the present invention has an average particle size of 3 to 25 μm. It is preferably 3 to 20 μm.

【0015】平均粒子径が3μm未満の場合、成形品の
黒色度は不充分であり、25μmを超える場合、成形性
が不良となる。
When the average particle size is less than 3 μm, the blackness of the molded product is insufficient, and when it exceeds 25 μm, the moldability becomes poor.

【0016】本発明に用いるステンレス粉末の配合量
は、40〜70重量%であることが肝要である。
It is important that the blending amount of the stainless powder used in the present invention is 40 to 70% by weight.

【0017】ステンレス粉末の配合量が40重量%未満
の場合、重量感に乏しく、70重量%を超える場合、成
形加工性及び成形品表面外観が不良となる。
When the content of the stainless steel powder is less than 40% by weight, the weight feeling is poor, and when it exceeds 70% by weight, the moldability and the surface appearance of the molded product become poor.

【0018】本発明に用いる(C)ガラス繊維は、熱可
塑性樹脂の強化用に使用されるものでよく、通常Eガラ
スやAガラスを材質とする。繊維径は通常5〜15μ
m、長さは3〜6mmが好ましい。
The glass fiber (C) used in the present invention may be one used for reinforcing a thermoplastic resin, and is usually made of E glass or A glass. Fiber diameter is usually 5-15μ
m, and the length is preferably 3 to 6 mm.

【0019】本発明に用いるガラス繊維の配合量は、5
〜15重量%であることが肝要である。5重量%未満の
場合、機械的強度が不良であり、15重量%を超える場
合は、成形品外観が不良になる。
The amount of glass fiber used in the present invention is 5
It is important that the content is -15% by weight. If it is less than 5% by weight, the mechanical strength is poor, and if it exceeds 15% by weight, the appearance of the molded product is poor.

【0020】本発明に用いる(D)カーボンブラック
は、通常樹脂の着色に用いられているものでよく、オイ
ルファーネスブラックやチャンネルブラック等が挙げら
れる。
The carbon black (D) used in the present invention may be one that is usually used for coloring resins, and examples thereof include oil furnace black and channel black.

【0021】本発明に用いるカーボンブラックの配合量
は、0.3〜2.0重量%であることが肝要である。
It is important that the amount of carbon black used in the present invention is 0.3 to 2.0% by weight.

【0022】カーボンブラックの配合量が0.3重量%
未満の場合、成形品の黒色度が不充分であり、2.0重
量%を超える場合は、機械的強度が不良となる。
Carbon black content of 0.3% by weight
If it is less than 2.0, the blackness of the molded product is insufficient, and if it exceeds 2.0% by weight, the mechanical strength becomes poor.

【0023】カーボンブラックは、(A)6ナイロンの
一部と共にマスターチップ化して、(A),(B),及
び(C)に混合する。
The carbon black is made into a master chip together with a part of (A) 6 nylon and mixed into (A), (B), and (C).

【0024】本発明では、上記一般式(I)で示される
(E)飽和脂肪族カルボン酸化合物を配合することが肝
要である。飽和脂肪族カルボン酸化合物は、式中のmが
14〜26の飽和脂肪族カルボン酸、またはその金属塩
あるいはそのエステルである。m=14の場合のパルミ
チン酸化合物、m=16の場合のステアリン酸化合物、
m=26の場合のモンタン酸化合物等が挙げられる。
In the present invention, it is essential to blend the (E) saturated aliphatic carboxylic acid compound represented by the above general formula (I). The saturated aliphatic carboxylic acid compound is a saturated aliphatic carboxylic acid in which m in the formula is 14 to 26, or a metal salt or ester thereof. palmitic acid compound when m = 14, stearic acid compound when m = 16,
Examples thereof include montanic acid compounds in the case of m = 26.

【0025】金属塩としては、リチウム、ナトリウム、
カリウム等のアルカリ金属、マグネシウム、カルシウム
等のアルカリ土類金属から成るものが挙げられる。
As the metal salt, lithium, sodium,
Examples thereof include those composed of alkali metals such as potassium and alkaline earth metals such as magnesium and calcium.

【0026】エステルとしては、エチレングリコール、
1,2−または1,3−プロパンジオール、1,3−ま
たは1,4−ブタンジオール等のアルコールでエステル
化したもの等が挙げられる。
As the ester, ethylene glycol,
Examples thereof include those esterified with alcohols such as 1,2- or 1,3-propanediol and 1,3- or 1,4-butanediol.

【0027】また、飽和脂肪族カルボン酸化合物は1種
でも、2種以上組み合わされたものでもよい。
The saturated aliphatic carboxylic acid compound may be one kind or a combination of two or more kinds.

【0028】かかる飽和脂肪族カルボン酸化合物として
は、ステアリン酸カルシウム、ステアリン酸マグネシウ
ム、モンタン酸ナトリウム、エチレングリコールでエス
テル化したモンタン酸エステル等が挙げられる。
Examples of the saturated aliphatic carboxylic acid compound include calcium stearate, magnesium stearate, sodium montanate, and montanic acid ester esterified with ethylene glycol.

【0029】本発明に用いる飽和脂肪族カルボン酸化合
物の配合量は、6ナイロン、SUS粉末及びガラス繊維
より成る組成物100重量部に対して、0.01〜0.
5重量部であることが肝要である。
The amount of the saturated aliphatic carboxylic acid compound used in the present invention is 0.01 to 0. 0 based on 100 parts by weight of the composition consisting of 6 nylon, SUS powder and glass fiber.
It is important that the amount is 5 parts by weight.

【0030】飽和脂肪族カルボン酸化合物の配合量が、
0.01重量部未満の場合、成形加工性不良となり、
0.5重量部を超える場合は、成形品外観が不良にな
る。
The amount of the saturated aliphatic carboxylic acid compound added is
If it is less than 0.01 part by weight, the molding processability becomes poor,
If it exceeds 0.5 parts by weight, the appearance of the molded product becomes poor.

【0031】飽和脂肪族カルボン酸化合物は、(A),
(B),(C),及び(D)の成分と共に混合して用い
ることができる。
The saturated aliphatic carboxylic acid compound is (A),
It can be used by mixing with the components (B), (C), and (D).

【0032】本発明の熱可塑性樹脂組成物には、本発明
の目的を損なわない範囲で必要に応じて通常の添加剤、
例えば、酸化防止剤及び熱安定剤(例えばヒンダードフ
ェノール,ヒドロキノン,チオエーテル,ホスファイト
類及びこれらの置換体及びその組合せを含む)、紫外線
吸収剤(例えば種々のレゾルシノール,サリシレート,
ベンゾトリアゾール,ベンゾフェノン等)、帯電防止剤
(例えばベンゼンスルホン酸ナトリウム,ポリアルキル
グリコール等)、結晶化促進剤(例えばポリエチレング
リコール等)、カップリング剤(例えばシラン系、チタ
ネート系、アルミニウム系等)、添加剤添着液(シリコ
ン系オイル等)を1種以上添加することができる。
The thermoplastic resin composition of the present invention may contain conventional additives, if necessary, within the range not impairing the object of the present invention.
For example, antioxidants and heat stabilizers (including hindered phenols, hydroquinones, thioethers, phosphites and their substitutions and combinations thereof), UV absorbers (eg various resorcinols, salicylates,
Benzotriazole, benzophenone, etc.), antistatic agent (eg sodium benzenesulfonate, polyalkyl glycol etc.), crystallization accelerator (eg polyethylene glycol etc.), coupling agent (eg silane type, titanate type, aluminum type etc.), One or more kinds of additive impregnating liquid (silicone oil, etc.) can be added.

【0033】本発明の熱可塑性樹脂組成物の製造方法
は、特に限定されるものではなく、公知の種々の方法を
とりうる。例えば、単軸或は、2軸混練機で溶融混練す
る方法が挙げられる。
The method for producing the thermoplastic resin composition of the present invention is not particularly limited, and various known methods can be used. For example, a method of melt-kneading with a single-screw or twin-screw kneader can be mentioned.

【0034】特にカーボンブラックは、粉末をそのまま
添加してもよいが一般には予めマスター化した物が用い
られる。
In particular, as carbon black, powder may be added as it is, but generally, a mastered product is used.

【0035】[0035]

【発明の効果】本発明の熱可塑性樹脂組成物は、機械的
強度に優れ、成形性及び成形品表面外観が良好であり、
更に成形品表面の黒色度が優れており、重量感があるた
め機械部品等に好適である。
EFFECT OF THE INVENTION The thermoplastic resin composition of the present invention has excellent mechanical strength, moldability and surface appearance of a molded product,
Further, the blackness of the surface of the molded product is excellent, and it has a heavy weight feeling, which is suitable for machine parts.

【0036】[0036]

【実施例】以下実施例によって本発明を具体的に発明す
る。尚、物性評価は以下の方法に従って行った。
The present invention will be concretely invented by the following examples. The physical properties were evaluated according to the following methods.

【0037】相対粘度:JIS K 6810 引張強度:ASTM D 638 成形品外観:目視による評価を行い、曇りの全くないも
のを◎、ほとんどないものを○、著しいものを×とし
た。 成形品黒色度:目視による評価を行い、黒色を◎、ほぼ
黒色を○、灰色を×とした。
Relative viscosity: JIS K 6810 Tensile strength: ASTM D 638 Appearance: The appearance of the molded product was evaluated by visual observation. A sample with no fog was marked with ⊚, a sample with almost no haze was marked with ◯, and a marked sample was marked with x. Molded product blackness: Visual evaluation was performed, and black was ⊚, almost black was ∘, and gray was x.

【0038】6ナイロンの製造例 ε−カプロラクタム100重量部、水1重量部を反応容
器に仕込み、密封して260℃まで加熱した。2〜3時
間そのままの圧力で反応させた後、500Torrの減
圧下で重合を進行させ、所定の粘度で重合を止め、押出
してペレット化し、更に熱水によりモノマーオリゴマー
を0.1%以下迄抽出し、6ナイロンを得た。
Production Example of 6 Nylon 100 parts by weight of ε-caprolactam and 1 part by weight of water were charged into a reaction vessel, sealed and heated to 260 ° C. After reacting under the same pressure for 2 to 3 hours, the polymerization is allowed to proceed under reduced pressure of 500 Torr, the polymerization is stopped at a predetermined viscosity, the mixture is extruded into pellets, and the monomer oligomer is extracted to 0.1% or less with hot water. Then, 6 nylon was obtained.

【0039】実施例1〜5,比較例1〜12 上記方法で得られた種々の粘度の6−ナイロン(表1に
記載)、SUS粉末(粒径50μmは大同特殊鋼株式会
社製、その他は大平洋金属株式会社製)、ガラス繊維
(T−289,日本電気硝子株式会社製)、飽和脂肪族
カルボン酸化合物,及び予め相対粘度2.3の6ナイロ
ンにカーボンブラック(チャンネルブラック)を20重
量%配合して練り込んで作ったカーボンブラックマスタ
ーを表1に示す組成で配合し、30mmスクリュウ径の
異方向回転2軸押出機で溶融混合してペレットを得た。
Examples 1-5, Comparative Examples 1-12 6-nylons of various viscosities (described in Table 1) obtained by the above method, SUS powder (particle size 50 μm manufactured by Daido Steel Co., Ltd., others) 20 weight of carbon black (channel black) to glass fiber (T-289, manufactured by Nippon Electric Glass Co., Ltd.), saturated aliphatic carboxylic acid compound, and 6 nylon having a relative viscosity of 2.3 in advance. % Carbon black master prepared by kneading and kneading was kneaded and kneaded, and melted and mixed by a counter-rotating twin-screw extruder having a screw diameter of 30 mm to obtain pellets.

【0040】得られたペレットを減圧下で加熱(120
℃)乾燥し、成形工程に共し、成形品を得て評価した。
結果を表2に示した。
The pellets obtained were heated under reduced pressure (120
(° C.), dried, and subjected to a molding step to obtain a molded product and evaluate it.
The results are shown in Table 2.

【0041】[0041]

【表1】 [Table 1]

【0042】[0042]

【表2】 [Table 2]

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 (A)相対粘度 2.1〜3.0の6
ナイロン,(B)平均粒子径 3〜25μmのステンレ
ス粉末40〜70重量%,(C)ガラス繊維5〜15重
量%,(D)カーボンブラック 0.3〜2.0重量
%,からなる組成物100重量部に対して、(E)下記
一般式(I)で示される飽和脂肪族カルボン酸化合物
0.01〜0.5重量部を配合してなることを特徴とす
る熱可塑性樹脂組成物。 〔CH3 (CH2 )m COO〕n R・・・・・(I) (式中mは14〜26の整数、nは1または2、Rはア
ルカリ金属、アルカリ土類金属、水素あるいは脂肪族炭
化水素基を表す。)
1. (A) Relative viscosity 2.1 to 3.0, 6
Composition comprising nylon, (B) 40 to 70% by weight of stainless powder having an average particle size of 3 to 25 μm, (C) 5 to 15% by weight of glass fiber, and (D) 0.3 to 2.0% by weight of carbon black. A thermoplastic resin composition comprising 100 parts by weight of 0.01 to 0.5 parts by weight of (E) a saturated aliphatic carboxylic acid compound represented by the following general formula (I). [CH 3 (CH 2) m COO] n R ····· (I) (an integer wherein m is 14 to 26, n is 1 or 2, R is an alkali metal, alkaline earth metal, hydrogen or fats Represents a group hydrocarbon group.)
JP33102894A 1994-12-07 1994-12-07 Thermoplastic resin composition Expired - Lifetime JP3261274B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP33102894A JP3261274B2 (en) 1994-12-07 1994-12-07 Thermoplastic resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP33102894A JP3261274B2 (en) 1994-12-07 1994-12-07 Thermoplastic resin composition

Publications (2)

Publication Number Publication Date
JPH08157715A true JPH08157715A (en) 1996-06-18
JP3261274B2 JP3261274B2 (en) 2002-02-25

Family

ID=18239021

Family Applications (1)

Application Number Title Priority Date Filing Date
JP33102894A Expired - Lifetime JP3261274B2 (en) 1994-12-07 1994-12-07 Thermoplastic resin composition

Country Status (1)

Country Link
JP (1) JP3261274B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1661954A1 (en) * 2004-11-27 2006-05-31 Degussa AG Thermoplastic powder formulation for coatings having metallic, particularly stainless steel colour imprint

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1661954A1 (en) * 2004-11-27 2006-05-31 Degussa AG Thermoplastic powder formulation for coatings having metallic, particularly stainless steel colour imprint

Also Published As

Publication number Publication date
JP3261274B2 (en) 2002-02-25

Similar Documents

Publication Publication Date Title
EP0204400A1 (en) Polypropylene-base resin composition
EP0096264A1 (en) Impact resistant polyamide mouldings
JPS58204043A (en) Reinforced polyolefin resin composition
GB1597478A (en) Polyamide blends
JPH02382B2 (en)
US4080349A (en) Glass-fiber-reinforced thermoplastic molding compositions showing improved flowability and toughness
US4423192A (en) Lubricated thermoplastic compositions of polyvinylidene fluoride
JPH01170641A (en) Polyacetal resin composition
JPH1053679A (en) Styrene polymer composition
JPS5936656B2 (en) Polypropylene Distillate Seibutsu
JPH08157715A (en) Flame-retardant resin composition
JPH0841318A (en) Thermoplastic resin composition
JPH0352953A (en) Polyamide resin composition
JPH10158461A (en) Thermoplastic resin composition and coated material made therefrom
JP2988860B2 (en) Thermoplastic resin composition
JPS6086162A (en) Polyamide resin composition
JP3388855B2 (en) Flame retardant resin composition
JPH0428748A (en) Acrylic resin composition
JPH048751A (en) Acrylic resin composition
JPH03152148A (en) Rigid chlorinated vinyl chloride-based resin composition for extrusion molding
JPS6136788B2 (en)
JPH08300389A (en) Production of resin molded product composed of styrene polymer composition
JPH03149246A (en) Production of vinyl chloride resin composition
JPH02292364A (en) Thermoplastic resin composition and its manufacture
JPS6357665A (en) Polyester resin composition

Legal Events

Date Code Title Description
S111 Request for change of ownership or part of ownership

Free format text: JAPANESE INTERMEDIATE CODE: R313113

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20081214

Year of fee payment: 7

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20091214

Year of fee payment: 8

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20091214

Year of fee payment: 8

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20101214

Year of fee payment: 9

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20101214

Year of fee payment: 9

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

S111 Request for change of ownership or part of ownership

Free format text: JAPANESE INTERMEDIATE CODE: R313113

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20101214

Year of fee payment: 9

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20101214

Year of fee payment: 9

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20111214

Year of fee payment: 10

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20111214

Year of fee payment: 10

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20121214

Year of fee payment: 11

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20121214

Year of fee payment: 11

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20131214

Year of fee payment: 12

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

EXPY Cancellation because of completion of term