JPH0753865A - Resin composition and molded product - Google Patents

Resin composition and molded product

Info

Publication number
JPH0753865A
JPH0753865A JP5199808A JP19980893A JPH0753865A JP H0753865 A JPH0753865 A JP H0753865A JP 5199808 A JP5199808 A JP 5199808A JP 19980893 A JP19980893 A JP 19980893A JP H0753865 A JPH0753865 A JP H0753865A
Authority
JP
Japan
Prior art keywords
weight
resin
molded product
resin composition
melt
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
JP5199808A
Other languages
Japanese (ja)
Other versions
JP3528208B2 (en
Inventor
Kazuhiko Kobayashi
和彦 小林
Atsushi Ishio
敦 石王
Kosuke Sakamoto
講輔 坂本
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.)
Toray Industries Inc
Original Assignee
Toray Industries Inc
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 Toray Industries Inc filed Critical Toray Industries Inc
Priority to JP19980893A priority Critical patent/JP3528208B2/en
Publication of JPH0753865A publication Critical patent/JPH0753865A/en
Application granted granted Critical
Publication of JP3528208B2 publication Critical patent/JP3528208B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29LINDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
    • B29L2011/00Optical elements, e.g. lenses, prisms
    • B29L2011/0083Reflectors

Abstract

PURPOSE:To provide the composition comprising a polyphenylene sulfide resin, a polyphenylene oxide, glass fibers having a small diameter and a filler, excellent in heat resistance, strength, rigidity, dimensional stability, moldability and surface smoothness, and useful for automotive lamp reflectors. CONSTITUTION:The composition comprises (A) 20-45wt.% of a polyphenylene sulfide resin, (B) 5-30wt.% of a polyphenylene oxide, (C) 0-15wt.% of glass fibers having a small fiber diameter of <=7mum, and (D) 25-75wt.%n of a non- fibrous inorganic filler, the components having been melt-kneaded. The component A preferably contains e.g. repeating units of formula I, and the component B preferably comprises e.g. constituting units of formula II (R1-R4 are H, halogen, 1-10C aliphatic, alicyclic or aromatic hydrocarbon), concretely poly(2,6- dimethyl-1,4-phenylene oxide), etc. The component D is preferably calcium carbonate, etc.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は耐熱性、剛性、寸法安定
性、成形加工性のすぐれたポリフェニレンスルフィド樹
脂(以下PPS樹脂と略す)組成物および該樹脂組成物
を射出成形して得られる表面平滑性、金属蒸着膜密着性
のすぐれた成形体に関するものであり、更に詳しくはP
PS樹脂とポリフェニレンオキシド樹脂(以下PPO樹
脂と略す)から主としてなる樹脂成分に非繊維状無機充
填材、必要に応じて特定の繊維径のガラス繊維を添加し
て溶融混練して得られる上記特性を有する樹脂組成物お
よび成形体に関するものである。
TECHNICAL FIELD The present invention relates to a polyphenylene sulfide resin (hereinafter abbreviated as PPS resin) composition having excellent heat resistance, rigidity, dimensional stability and molding processability, and a surface obtained by injection molding the resin composition. The present invention relates to a molded product having excellent smoothness and adhesion to a metal vapor deposition film.
The above characteristics obtained by melt-kneading by adding a non-fibrous inorganic filler and, if necessary, a glass fiber having a specific fiber diameter to a resin component mainly composed of a PS resin and a polyphenylene oxide resin (hereinafter abbreviated as PPO resin) The present invention relates to a resin composition and a molded product having the same.

【0002】[0002]

【従来の技術】自動車部品、特にエンジンルーム内の部
品や電装部品、機能部品などが金属からプラスチックに
徐々に代替されてきていることはよく知られていること
である。これはプラスチックが金属にくらべて軽量であ
り、製品のデザインの自由度が大きく、しかも元々複数
の部品を一体成形することにより、生産性の向上が可能
となることがおもな理由である。機能部品の代表的なも
のの一つにランプリフレクターがある。ランプリフレク
ターは従来主に不飽和ポリエステルBMCなどの熱硬化
性樹脂あるいはアルミニウム製のものが使用されてい
る。熱硬化性樹脂製リフレクターはアルミニウム製に比
べれば軽量であるが、現状では比重が2.0を越えるた
め、一層の軽量化が求められており、また熱硬化性樹脂
に特有の成形品後処理作業の煩雑さ、粉塵などによる作
業環境汚染などの問題があり、熱可塑性樹脂材料への転
換が求められている。PPS樹脂は耐熱性、剛性、寸法
安定性にすぐれ、充填材との親和性が良く、成形加工性
も良好であることからランプリフレクター用材料として
ポテンシャルが高く、これまでにも軽量化を目的にPP
Sと特定の中空充填材を組み合わせた組成物を射出成形
して得られるランプリフレクター(例えば特開平3−2
08201号公報)、表面平滑性と強度向上を目的にP
PSと特定径の繊維状強化材を組み合わせた組成物を射
出成形して得られるランプリフレクター(例えば特開平
4−334801号公報)などが提案されている。
2. Description of the Related Art It is well known that automobile parts, particularly parts in an engine room, electrical parts, functional parts, etc. are gradually replaced by metal from plastic. The main reason for this is that plastic is lighter in weight than metal, has a high degree of freedom in designing products, and can originally improve productivity by integrally molding a plurality of parts. One of the representative functional parts is a lamp reflector. As the lamp reflector, a thermosetting resin such as unsaturated polyester BMC or one made of aluminum has been mainly used conventionally. Thermosetting resin reflectors are lighter than aluminum ones, but at present the specific gravity exceeds 2.0, so further weight reduction is required, and the post treatment of molded products peculiar to thermosetting resins is required. Since there are problems such as complexity of work and work environment pollution due to dust and the like, conversion to a thermoplastic resin material is required. PPS resin has excellent heat resistance, rigidity, dimensional stability, good compatibility with fillers, and good moldability, so it has a high potential as a material for lamp reflectors, and it has been aiming for weight reduction until now. PP
A lamp reflector obtained by injection molding a composition in which S and a specific hollow filler are combined (for example, JP-A-3-2).
08201), P for the purpose of improving surface smoothness and strength.
A lamp reflector (for example, Japanese Patent Laid-Open No. 4-334801) obtained by injection molding a composition in which PS and a fibrous reinforcing material having a specific diameter are combined has been proposed.

【0003】しかしこれら従来技術では射出成形時の樹
脂の流れ方向とその垂直方向の成形収縮率の差に起因す
る成形品そりや後加工工程におけるアルミニウム蒸着膜
との密着性不足などの問題があり、これらの改良が強く
求められているのが現状である。一方寸法安定性の極め
て良好なPPO樹脂の成形加工性(流動性)向上を目的
としてPPS樹脂と配合する技術も開示されている(例
えば特公昭56−34032号公報など)が、この技術
のリフレクター用途への応用については示されていな
い。
However, in these conventional techniques, there are problems such as a warp of a molded product due to a difference in molding shrinkage between a resin flow direction and a vertical direction at the time of injection molding and insufficient adhesion to an aluminum vapor deposition film in a post-processing step. At present, there is a strong demand for these improvements. On the other hand, a technique of blending with a PPS resin for the purpose of improving the molding processability (fluidity) of a PPO resin having extremely good dimensional stability is disclosed (for example, Japanese Patent Publication No. 56-34032), but the reflector of this technique is disclosed. No application to the application is shown.

【0004】[0004]

【発明が解決しようとする課題】そこで本発明は耐熱
性、剛性、寸法安定性、成形加工性のすぐれた熱可塑性
樹脂組成物および該樹脂組成物を射出成形して得られる
表面平滑性、金属蒸着膜密着性のすぐれた成形体を得る
ことを課題とする。
Therefore, the present invention is directed to a thermoplastic resin composition having excellent heat resistance, rigidity, dimensional stability, and moldability, and surface smoothness and metal obtained by injection molding of the resin composition. It is an object to obtain a molded product having excellent adhesion to a deposited film.

【0005】この課題解決のために鋭意検討した結果、
PPS樹脂とPPO樹脂から主としてなる樹脂成分に非
繊維状無機充填材と必要に応じて特定の繊維径のガラス
繊維とを添加して得られる樹脂組成物および成形体が上
記要求特性を十分満足するものであることを見出し、本
発明に到達した。
As a result of earnest studies for solving this problem,
A resin composition and a molded product obtained by adding a non-fibrous inorganic filler and, if necessary, a glass fiber having a specific fiber diameter to a resin component mainly composed of a PPS resin and a PPO resin satisfy the above-mentioned required characteristics. The present invention has been achieved by finding out that it is a thing.

【0006】[0006]

【課題を解決するための手段】すなわち本発明は、
(A)ポリフェニレンスルフィド樹脂20〜45重量
%、(B)ポリフェニレンオキシド5〜30重量%、
(C)繊維径7μm以下の細径ガラス繊維0〜15重量
%および(D)非繊維状無機充填材25〜75重量%か
らなる混合物を溶融混練することにより得ることを特徴
とする樹脂組成物および該樹脂組成物を射出成形するこ
とにより得られる表面平滑性のすぐれた成形体である。
That is, the present invention is as follows.
(A) Polyphenylene sulfide resin 20 to 45% by weight, (B) Polyphenylene oxide 5 to 30% by weight,
A resin composition obtained by melt-kneading a mixture of (C) 0 to 15% by weight of fine glass fibers having a fiber diameter of 7 μm or less and (D) 25 to 75% by weight of a non-fibrous inorganic filler. And a molded article having excellent surface smoothness obtained by injection molding the resin composition.

【0007】本発明で使用する(A)PPS樹脂とは、
構造式(I)で示される繰り返し単位を
The (A) PPS resin used in the present invention is
The repeating unit represented by the structural formula (I)

【化1】 70モル%以上、より好ましくは90モル%以上を含む
重合体であり、上記繰り返し単位が70モル%未満で
は、耐熱性が損なわれるので好ましくない。またPPS
樹脂はその繰り返し単位の30モル%未満を、下記の構
造式を有する繰り返し単位で構成することが可能であ
る。
[Chemical 1] It is a polymer containing 70 mol% or more, more preferably 90 mol% or more, and if the repeating unit is less than 70 mol%, heat resistance is impaired, which is not preferable. Also PPS
The resin can comprise less than 30 mol% of its repeating units with repeating units having the following structural formula.

【0008】[0008]

【化2】 本発明で用いられるPPS樹脂の溶融粘度は、溶融混練
が可能であれば特に制限はないが、通常50〜20,0
00ポアズ(320℃、剪断速度10sec-1)のもの
が使用される。
[Chemical 2] The melt viscosity of the PPS resin used in the present invention is not particularly limited as long as it can be melt-kneaded, but is usually 50 to 20,0.
A 00 poise (320 ° C., shear rate 10 sec −1 ) is used.

【0009】かかるPPS樹脂は通常公知の方法即ち特
公昭45−3368号公報に記載される比較的分子量の
小さな重合体を得る方法あるいは特公昭52−1224
0号公報や特開昭61−7332号公報に記載される比
較的分子量の大きな重合体を得る方法などによって製造
できる。本発明において上記のように得られたPPS樹
脂を空気中加熱による架橋/高分子量化、有機溶媒、熱
水、酸水溶液などによる洗浄、酸無水物基、エポキシ
基、アミノ基、イソシアネート基などの官能基含有化合
物による活性化など種々の処理を施した上で使用するこ
とももちろん可能である。
Such a PPS resin is a known method, that is, a method for obtaining a polymer having a relatively small molecular weight as described in JP-B-45-3368 or JP-B-52-1224.
It can be produced by the method of obtaining a polymer having a relatively large molecular weight described in JP-A-No. In the present invention, the PPS resin obtained as described above is subjected to crosslinking / polymerization by heating in air, washing with an organic solvent, hot water, an aqueous acid solution, an acid anhydride group, an epoxy group, an amino group, an isocyanate group, etc. Of course, it is possible to use it after various treatments such as activation with a functional group-containing compound.

【0010】本発明で用いられる(B)PPO樹脂とは
下記構造式(II)で示される構成単位から基本的にな
り、
The (B) PPO resin used in the present invention basically comprises a structural unit represented by the following structural formula (II),

【化3】 (ここでR1,R2、R3およびR4はそれぞれ水素原
子、ハロゲン原子、炭素数1〜10の脂肪族、脂環族、
芳香族の炭化水素基を表わし、R1〜R4は互いに同じ
でも異なっていてもよい。)還元粘度(0.5g/dl
クロロホルム溶液、30℃測定)が0.15〜0.70
の範囲にある単独重合体および/または共重合体であ
る。かかるPPOの具体例としては、ポリ(2,6−ジ
メチル−1,4−フェニレンオキシド)、ポリ(2−メ
チル−6−エチル−1,4−フェニレンオキシド)、ポ
リ(2,6−ジフェニル−1,4−フェニレンオキシ
ド)、ポリ(2−メチル−6−フェニル−1,4−フェ
ニレンオキシド)、ポリ(2,6−ジクロロ−1,4−
フェニレンオキシド)などを挙げることができ、さらに
2,6−ジメチルフェノールと他のフェノール類(例え
ば2,3,6−トリメチルフェノール)との共重合体の
ごとき共重合体が挙げられる。なかでも、ポリ(2,6
−ジメチル−1,4−フェニレンオキシド)、2,6−
ジメチルフェノールと2,3,6−トリメチルフェノー
ルとの共重合体が好ましく、特にポリ(2,6−ジメチ
ル−1,4−フェニレンオキシド)が好ましい。
[Chemical 3] (Here, R1, R2, R3, and R4 are each a hydrogen atom, a halogen atom, an aliphatic group having 1 to 10 carbon atoms, an alicyclic group,
It represents an aromatic hydrocarbon group, and R1 to R4 may be the same or different from each other. ) Reduced viscosity (0.5 g / dl
Chloroform solution, measured at 30 ° C) is 0.15 to 0.70
Is a homopolymer and / or a copolymer within the range. Specific examples of such PPO include poly (2,6-dimethyl-1,4-phenylene oxide), poly (2-methyl-6-ethyl-1,4-phenylene oxide), poly (2,6-diphenyl-). 1,4-phenylene oxide), poly (2-methyl-6-phenyl-1,4-phenylene oxide), poly (2,6-dichloro-1,4-)
Phenylene oxide) and the like, and further, a copolymer such as a copolymer of 2,6-dimethylphenol and other phenols (for example, 2,3,6-trimethylphenol). Among them, poly (2,6
-Dimethyl-1,4-phenylene oxide), 2,6-
A copolymer of dimethylphenol and 2,3,6-trimethylphenol is preferable, and poly (2,6-dimethyl-1,4-phenylene oxide) is particularly preferable.

【0011】かかるPPOの製造方法は特に制限される
ものではなく、公知の方法で得られるものを用いること
ができる。例えば、米国特許第3306874号明細書
記載のHayによる第一銅塩とアミンのコンプレックス
を触媒として酸化重合することにより容易に製造でき
る。本発明においては上記のようにして得られたPPO
をさらに酸無水物基、エポキシ基、アミノ基、イソシア
ネート基などの官能基含有化合物によって変性または活
性化など種々の処理を施した上で使用することももちろ
ん可能である。
The method for producing such PPO is not particularly limited, and those obtained by known methods can be used. For example, it can be easily produced by oxidative polymerization using a complex of cuprous salt and amine by Hay described in US Pat. No. 3,306,874 as a catalyst. In the present invention, the PPO obtained as described above
It is, of course, possible to use the above after undergoing various treatments such as modification or activation with a compound containing a functional group such as an acid anhydride group, an epoxy group, an amino group or an isocyanate group.

【0012】本発明において使用される非繊維状充填材
は材料の寸法安定性向上のために必要な成分であり、そ
の具体例としては、ワラステナイト、セリサイト、カオ
リン、マイカ、クレー、ベントナイト、アスベスト、タ
ルク、アルミナシリケートなどの珪酸塩、アルミナ、酸
化珪素、酸化マグネシウム、酸化ジルコニウム、酸化チ
タン、酸化鉄などの金属化合物、炭酸カルシウム、炭酸
マグネシウム、ドロマイトなどの炭酸塩、硫酸カルシウ
ム、硫酸バリウムなどの硫酸塩、ガラス・ビーズ、セラ
ミックビーズ、窒化ホウ素、炭化珪素、燐酸カルシウム
およびシリカなどが挙げられ、これらは中空であっても
よく、さらにはこれら充填材を2種類以上併用すること
も可能である。また、これら非繊維状充填材をシラン系
あるいはチタネート系、アルミニウム系などのカップリ
ング剤で予備処理して使用することは、機械的強度など
の面からより好ましい。
The non-fibrous filler used in the present invention is a component necessary for improving the dimensional stability of the material, and specific examples thereof include wollastonite, sericite, kaolin, mica, clay, bentonite, Silicates such as asbestos, talc, alumina silicate, alumina, silicon oxide, magnesium oxide, zirconium oxide, metal compounds such as titanium oxide and iron oxide, carbonates such as calcium carbonate, magnesium carbonate, dolomite, calcium sulfate, barium sulfate, etc. Examples thereof include sulfates, glass beads, ceramic beads, boron nitride, silicon carbide, calcium phosphate, and silica, which may be hollow, and two or more kinds of these fillers may be used in combination. is there. In addition, it is more preferable to use these non-fibrous fillers after pre-treating them with a coupling agent such as a silane-based, titanate-based, or aluminum-based filler from the viewpoint of mechanical strength and the like.

【0013】本発明において繊維状強化材として、単糸
径7μm以下の細径ガラス繊維をさらに配合することに
より耐熱性、強度が向上する。ランプリフレクターに要
求される耐熱性、強度、剛性を満たすためには繊維状の
強化材を添加する場合があるが、このとき通常熱可塑性
樹脂用強化材として用いられる単糸径7μmを越えるガ
ラス繊維を用いると成形品の表面平滑性が著しく損なわ
れる。好ましく使用されるガラス繊維の単糸径は6μm
以下、さらに好ましくは3μm以下である。
In the present invention, as a fibrous reinforcing material, heat resistance and strength are improved by further blending fine glass fibers having a single yarn diameter of 7 μm or less. In order to satisfy the heat resistance, strength and rigidity required for the lamp reflector, a fibrous reinforcing material may be added. At this time, a glass fiber having a single yarn diameter of more than 7 μm which is usually used as a reinforcing material for thermoplastic resin. If used, the surface smoothness of the molded product is significantly impaired. Single fiber diameter of glass fiber used preferably is 6 μm
Hereafter, it is more preferably 3 μm or less.

【0014】本発明の樹脂組成物における各成分の配合
割合はPPS樹脂20〜45重量%、PPO樹脂5〜3
0重量%、非繊維状無機充填材25〜75重量%および
単糸径7μm以下の細径ガラス繊維0〜15重量%の範
囲であり、PPS樹脂25〜40重量%、PPO樹脂1
0〜25重量%、非繊維状無機充填材30〜70重量%
および単糸径7μm以下の細径ガラス繊維3〜10重量
%の範囲であることが好ましい。上記配合割合において
のみランプリフレクターに要求される耐熱性、強度、剛
性、寸法安定性、成形加工性および表面平滑性、金属蒸
着膜密着性のすべての特性を満足する樹脂組成物および
その成形体が得られるのである。たとえばPPO樹脂の
配合量が5重量%に満たないと金属蒸着膜の密着性が不
足し、逆に配合量が30重量%を越えると流動性が低下
し、溶融成形加工が困難になる。また非繊維状無機充填
材配合量が25重量%に満たないと耐熱性、寸法安定性
が不足し、逆に配合量が75重量%を越えると流動性が
低下し、溶融成形加工が困難になり、表面平滑性の低下
が著しくなる。さらに細径ガラス繊維の配合量が15重
量%を越えると表面平滑性の低下が著しくなる。
The compounding ratio of each component in the resin composition of the present invention is 20 to 45% by weight of PPS resin and 5 to 3 of PPO resin.
0% by weight, 25 to 75% by weight of non-fibrous inorganic filler, and 0 to 15% by weight of fine glass fibers having a single yarn diameter of 7 μm or less, PPS resin 25 to 40% by weight, PPO resin 1
0-25% by weight, non-fibrous inorganic filler 30-70% by weight
Also, the range of 3 to 10% by weight of fine glass fiber having a single yarn diameter of 7 μm or less is preferable. A resin composition and a molded product thereof satisfying all the properties of heat resistance, strength, rigidity, dimensional stability, molding processability and surface smoothness, and metal vapor deposition film adhesiveness required for a lamp reflector only in the above mixing ratio are provided. You can get it. For example, if the blending amount of the PPO resin is less than 5% by weight, the adhesion of the vapor-deposited metal film will be insufficient, and conversely if the blending amount exceeds 30% by weight, the fluidity will be lowered and the melt molding process will be difficult. If the content of the non-fibrous inorganic filler is less than 25% by weight, heat resistance and dimensional stability will be insufficient, and conversely, if the content of the non-fibrous inorganic filler exceeds 75% by weight, the fluidity will be lowered, making the melt molding process difficult. And the surface smoothness is significantly reduced. Further, when the compounding amount of the fine glass fiber exceeds 15% by weight, the surface smoothness is remarkably deteriorated.

【0015】本発明のPPS樹脂組成物には、本発明の
目的を損なわない範囲で、酸化防止剤および熱安定剤
(たとえばヒンダードフェノール、ヒドロキノン、ホス
ファイト類およびこれらの置換体など)、紫外線吸収剤
(たとえばレゾルシノール、サリシレート、ベンゾトリ
アゾール、ベンゾフェノンなど)、滑剤および離型剤
(モンタン酸およびその塩、そのエステル、そのハーフ
エステル、ステアリルアルコール、ステアラミドおよび
ポリエチレンワックスなど)、染料(たとえばニグロシ
ンなど)および顔料(たとえば硫化カドミウム、フタロ
シアニン、カーボンブラックなど)を含む着色剤、可塑
剤、難燃剤、難燃助剤、帯電防止剤などの通常の添加剤
や他の熱可塑性樹脂(たとえばポリアミド、ポリスルホ
ン、四フッ化ポリエチレン、ポリエーテルイミド、ポリ
アミドイミド、ポリイミド、ポリカーボネート、ポリエ
ーテルスルホン、ポリエーテルケトン、ポリエーテルエ
ーテルケトン、エポキシ樹脂、フェノール樹脂、ポリエ
チレン、ポリスチレン、ポリプロピレン、ABS樹脂、
ポリエステル、ポリアミドエラストマ、ポリエステルエ
ラストマ等の樹脂)を添加して、所定の特性を付与する
ことができる。
The PPS resin composition of the present invention contains an antioxidant and a heat stabilizer (for example, hindered phenol, hydroquinone, phosphites and their substitution products), ultraviolet rays, etc. within a range not impairing the object of the present invention. Absorbents (eg resorcinol, salicylate, benzotriazole, benzophenone etc.), lubricants and mold release agents (montanic acid and its salts, its esters, its half esters, stearyl alcohol, stearamide and polyethylene wax etc.), dyes (eg nigrosine etc.) And conventional additives such as colorants, including pigments (eg, cadmium sulfide, phthalocyanine, carbon black, etc.), plasticizers, flame retardants, flame retardant aids, antistatic agents and other thermoplastic resins (eg polyamide, polysulfone, Polytetrafluoroethylene Emissions, polyetherimide, polyamideimide, polyimide, polycarbonate, polyether sulfone, polyether ketone, polyether ether ketone, epoxy resin, phenol resin, polyethylene, polystyrene, polypropylene, ABS resin,
Resins such as polyester, polyamide elastomer, and polyester elastomer) can be added to impart predetermined characteristics.

【0016】本発明のPPS樹脂組成物には本発明の効
果を損なわない範囲で、機械的強度およびバリ等の成形
性などの改良を目的として、γ−グリシドキシプロピル
トリメトキシシラン、γーグリシドキシプロピルトリエ
トキシシラン、β−(3,4−エポキシシクロヘキシ
ル)エチルトリメトキシシラン、γーメルカプトプロピ
ルトリメトキシシラン、γ−メルカプトプロピルトリエ
トキシシラン、γーウレイドプロピルトリエトキシシラ
ン、γーウレイドプロピルトリメトキシシランおよびγ
ー(2−ウレイドエチル)アミノプロピルトリメトキシ
シラン、γーイソシアナトプロピルトリエトキシシラ
ン、γーイソシアナトプロピルトリメトキシシラン、γ
ーイソシアナトプロピルメチルジメトキシシラン、γー
イソシアナトプロピルメチルジエトキシシラン、γーイ
ソシアナトプロピルエチルジメトキシシラン、γーイソ
シアナトプロピルエチルジエトキシシラン、γーイソシ
アナトプロピルトリクロロシラン、γーアミノプロピル
トリメトキシシラン、γーアミノプロピルトリエトキシ
シランなどの有機シラン化合物を添加することができ
る。
The PPS resin composition of the present invention contains γ-glycidoxypropyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, and γ-, for the purpose of improving mechanical strength and moldability such as burr, etc. within a range not impairing the effects of the present invention. Glycidoxypropyltriethoxysilane, β- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, γ-mercaptopropyltrimethoxysilane, γ-mercaptopropyltriethoxysilane, γ-ureidopropyltriethoxysilane, γ-ureido Propyltrimethoxysilane and γ
-(2-ureidoethyl) aminopropyltrimethoxysilane, γ-isocyanatopropyltriethoxysilane, γ-isocyanatopropyltrimethoxysilane, γ
-Isocyanatopropylmethyldimethoxysilane, γ-isocyanatopropylmethyldiethoxysilane, γ-isocyanatopropylethyldimethoxysilane, γ-isocyanatopropylethyldiethoxysilane, γ-isocyanatopropyltrichlorosilane, γ-aminopropyltrisilane Organosilane compounds such as methoxysilane and γ-aminopropyltriethoxysilane can be added.

【0017】本発明のPPS樹脂組成物は十分な混練力
を有する溶融混練機を用いて溶融混練により製造するこ
とが簡便、かつ所期の特性を発現し得る点から適してい
る。溶融混練には公知の方法を用いることができ、たと
えばバンバリーミキサー、ゴムロール機、ニーダー、単
軸もしくは二軸押出機などを用い、270〜380℃の
温度で溶融混練して組成物とすることができる。原料の
混合順序には特に制限はなく、PPS樹脂、PPO樹脂
および繊維状および/または非繊維状充填材の3者をド
ライブレンドした後、上述の方法などで溶融混練する方
法、あるいはPPS樹脂、繊維状および/または非繊維
状充填材およびPPO樹脂のうちの2者をドライブレン
ドして溶融混練した後、これと残る1者を溶融混練する
方法を用いることも可能である。
The PPS resin composition of the present invention is suitable for production by melt-kneading using a melt-kneading machine having a sufficient kneading force, since the desired characteristics can be exhibited. A known method can be used for the melt kneading, and for example, a Banbury mixer, a rubber roll machine, a kneader, a single-screw or twin-screw extruder can be used to melt-knead at a temperature of 270 to 380 ° C. to obtain a composition. it can. The order of mixing the raw materials is not particularly limited, and a method of dry-blending PPS resin, PPO resin and fibrous and / or non-fibrous filler, and then melt-kneading by the above-mentioned method, or PPS resin, It is also possible to use a method in which two of the fibrous and / or non-fibrous filler and the PPO resin are dry-blended, melt-kneaded, and then the remaining one is melt-kneaded.

【0018】かくして得られる本発明のPPS樹脂組成
物を射出成形することにより、表面平滑性のすぐれた成
形体を得ることができる。この成形体は表面平滑性、金
属蒸着膜密着性、寸法安定性、耐熱性、強度、成形加工
性にすぐれるのでこれらの特性を活かして種々の電気、
電装、自動車などの部品とすることができ、特にランプ
リフレクター基体として有用であり、アルミニウム等の
金属蒸着をすることにより、極めて実用的なランプリフ
レクターを得ることができる。
By molding the PPS resin composition of the present invention thus obtained by injection molding, a molded article having excellent surface smoothness can be obtained. This molded product has excellent surface smoothness, adhesion to metal vapor deposition film, dimensional stability, heat resistance, strength, and molding processability.
It can be used as a component of electric equipment, automobiles, etc., and is particularly useful as a lamp reflector base, and a very practical lamp reflector can be obtained by vapor deposition of a metal such as aluminum.

【0019】[0019]

【実施例】以下、実施例により本発明をさらに詳述す
る。なお実施例および比較例に記された特性は次の方法
で測定した。
EXAMPLES The present invention will be described in more detail below with reference to examples. The properties described in Examples and Comparative Examples were measured by the following methods.

【0020】(1)成形品の比重:水中置換法 (2)成形収縮率:80×80×3mmの角板を射出成
形し、その流れ方向と垂直方向の成形収縮率を金型原寸
に対して測定した。
(1) Specific gravity of molded product: underwater substitution method (2) Molding shrinkage ratio: 80 × 80 × 3 mm square plate is injection molded, and the molding shrinkage ratio in the direction perpendicular to the flow direction is the original size of the mold. Measured.

【0021】(3)曲げ強度:ASTM D790 (4)熱変形温度:ASTM D648 (5)表面平滑性:80×80×3mmの角板の表面の
光沢度を携帯用鮮明度光沢度計PGD−IV(日本色彩研
究所、東京光電(株)製)を用いて測定した。この数値
が高いほど表面が平滑で反射像が鮮明である。
(3) Bending strength: ASTM D790 (4) Heat distortion temperature: ASTM D648 (5) Surface smoothness: 80 × 80 × 3 mm square plate surface gloss was measured with a portable sharpness gloss meter PGD- It was measured using IV (Japan Color Research Laboratory, Tokyo Koden Co., Ltd.). The higher this value, the smoother the surface and the clearer the reflected image.

【0022】(6)蒸着膜密着性:射出成形で得た成形
基体表面に真空蒸着法でアルミニウムを蒸着せしめ、そ
の鏡面にカミソリで5mm間隔で格子状に切り込みを入
れ、100個のマス目を作った。次に表面にセロテープ
を貼った後一気に引き剥がす操作を行った。上記操作の
後に成形体表面に残った金属塗膜のマス目の数を数えて
密着性の目安とした。
(6) Adhesion of deposited film: Aluminum is deposited on the surface of a molded substrate obtained by injection molding by a vacuum deposition method, and the mirror surface is cut with a razor at intervals of 5 mm in a grid pattern to form 100 squares. Had made. Next, an operation of sticking cellophane on the surface and then peeling it off at once was performed. After the above operation, the number of squares of the metal coating film remaining on the surface of the molded body was counted and used as a measure of adhesion.

【0023】参考例1(ポリフェニレンスルフィドの合
成法) PPS−1:オートクレーブに硫化ナトリウム3.26
Kg(25モル、結晶水40%を含む)、水酸化ナトリ
ウム4g、酢酸ナトリウム三水和物0.41Kg(約3
モル)およびNMP7.9Kgを仕込み、撹拌しながら
徐々に205℃まで昇温し、水1.36Kgを含む留出
水約1.5リットルを除去した。残留混合物に1,4−
ジクロロベンゼン3.75Kg(25.5モル)および
NMP2Kgを加え、265℃で3.7時間加熱した。
反応生成物を70℃の温水で5回洗浄し、80℃で24
時間減圧乾燥して、溶融粘度約400ポアズ(310
℃、剪断速度1000秒−1)の粉末状ポリフェニレン
スルフィド(PPS−1)約2Kgを得た。
Reference Example 1 (Synthesis Method of Polyphenylene Sulfide) PPS-1: Sodium Sulfide 3.26 in Autoclave
Kg (25 mol, containing 40% of water of crystallization), sodium hydroxide 4 g, sodium acetate trihydrate 0.41 Kg (about 3
Mol) and NMP 7.9 Kg were charged, the temperature was gradually raised to 205 ° C. with stirring, and about 1.5 liters of distilled water containing 1.36 Kg of water was removed. 1,4-to the residual mixture
3.75 kg (25.5 mol) of dichlorobenzene and 2 kg of NMP were added, and the mixture was heated at 265 ° C for 3.7 hours.
The reaction product was washed 5 times with hot water at 70 ° C and then washed at 80 ° C for 24 hours.
After being dried under reduced pressure for about an hour, the melt viscosity is about 400 poise (310
Approximately 2 kg of powdery polyphenylene sulfide (PPS-1) at a temperature of 1000 ° C. and a shear rate of 1000 sec −1 was obtained.

【0024】PPS−2:オートクレーブに硫化ナトリ
ウム3.26Kg(25モル、結晶水40%を含む)、
水酸化ナトリウム4g、酢酸ナトリウム三水和物1.1
9Kg(約8.8モル)およびNMP7.9Kgを仕込
み、撹拌しながら徐々に205℃まで昇温し、水1.3
6Kgを含む留出水約1.5リットルを除去した。残留
混合物に1,4−ジクロロベンゼン3.75Kg(2
5.5モル)およびNMP2Kgを加え、265℃で3
時間加熱した。反応生成物を70℃の温水で5回洗浄
し、80℃で24時間減圧乾燥して、溶融粘度約600
ポアズ(310℃、剪断速度1000秒−1)の粉末状
ポリフェニレンスルフィド(PPS−2)約2Kgを得
た。
PPS-2: 3.26 kg of sodium sulfide (25 mol, containing 40% of water of crystallization) in an autoclave,
Sodium hydroxide 4g, sodium acetate trihydrate 1.1
9 Kg (about 8.8 mol) and NMP 7.9 Kg were charged, the temperature was gradually raised to 205 ° C. with stirring, and water 1.3
About 1.5 liters of distilled water containing 6 kg was removed. To the residual mixture, 3.75 Kg of 1,4-dichlorobenzene (2
5.5 mol) and 2 Kg of NMP are added and the mixture is mixed at 265 ° C. for 3
Heated for hours. The reaction product was washed 5 times with hot water at 70 ° C and dried under reduced pressure at 80 ° C for 24 hours to obtain a melt viscosity of about 600.
About 2 kg of powdery polyphenylene sulfide (PPS-2) having a poise (310 ° C, shear rate 1000 sec -1 ) was obtained.

【0025】また、PPS−3としては東レ(株)製、
M2900を使用した。
The PPS-3 is manufactured by Toray Industries, Inc.
M2900 was used.

【0026】実施例1 PPS樹脂(PPS−1)28重量%,PPO樹脂とし
てポリ(2,6−ジメチル−1,4−フェニレンオキシ
ド)(還元粘度0.45)12重量%、単糸径6μmの
ガラス繊維3重量%および炭酸カルシウム57重量%を
ヘンシェルミキサーでドライブレンドした後、320℃
のシリンダー温度に設定したスクリュー式2軸押出機に
より溶融混練後ペレタイズした。得られたペレットを乾
燥後射出成形機を用いて、シリンダー温度320℃、金
型温度150℃の条件で射出成形することにより、所定
の特性評価用試験片および乗用車ヘッドライト用ランプ
リフレクター基体成形品を得た。得られた試験片につい
て行った測定結果を表1にまとめて示す。ここで得られ
た樹脂組成物は強度、耐熱性にすぐれ、しかも極めてす
ぐれた表面平滑性を有し、自動車用ランプリフレクター
用として好適なものであった。また、ランプリフレクタ
ー基体成形品については脱脂後直接真空蒸着法によって
アルミニウム蒸着を行ない、その密着性を評価した。結
果は表1に示す通り、ここで得られたランプリフレクタ
ーは良好な表面性と密着性を有する実用価値の高いもの
であった。
Example 1 28% by weight of PPS resin (PPS-1), 12% by weight of poly (2,6-dimethyl-1,4-phenylene oxide) (reduced viscosity 0.45) as PPO resin, single yarn diameter of 6 μm After dry blending 3% by weight of glass fiber and 57% by weight of calcium carbonate with a Henschel mixer,
After melt-kneading and pelletizing with a screw type twin-screw extruder set to the cylinder temperature of. The obtained pellets are dried and then injection-molded using an injection molding machine under the conditions of a cylinder temperature of 320 ° C. and a mold temperature of 150 ° C. to obtain a predetermined test piece for characteristic evaluation and a lamp reflector base molded article for a passenger car headlight. Got The measurement results of the obtained test pieces are summarized in Table 1. The resin composition obtained here had excellent strength and heat resistance, and also had extremely excellent surface smoothness, and was suitable for use as a lamp reflector for automobiles. Further, the molded product of the lamp reflector substrate was subjected to direct vapor deposition of aluminum after degreasing, and its adhesion was evaluated. The results are shown in Table 1, and the lamp reflector obtained here had good surface properties and adhesion, and was of high practical value.

【0027】[0027]

【表1】 比較例1 PPO樹脂を配合せず、PPS樹脂の配合量を40重量
%とした以外は実施例1と全く同様に溶融混練、射出成
形および特性評価を実施した。ここで得られた樹脂組成
物は成形収縮が大きく寸法安定性が劣っており、さらに
このものを射出成形して得られたランプリフレクター基
体成形品についても実施例1と同様に真空蒸着法によっ
てアルミニウム蒸着を行ない、その密着性を評価したが
結果は表1に示す通り、密着性不足であった。
[Table 1] Comparative Example 1 Melt kneading, injection molding and property evaluation were performed in exactly the same manner as in Example 1 except that the PPO resin was not compounded and the PPS resin compounded amount was 40% by weight. The resin composition obtained here had a large molding shrinkage and poor dimensional stability, and a lamp reflector substrate molded product obtained by injection molding this resin was also subjected to the same vacuum evaporation method as in Example 1 by the aluminum vapor deposition method. Vapor deposition was performed and the adhesiveness was evaluated, but the result was insufficient adhesiveness as shown in Table 1.

【0028】比較例2 ガラス繊維および炭酸カルシウムの配合量を各々20、
40重量%とした以外は実施例1と全く同様に溶融混
練、射出成形および特性評価を実施した。ここで得られ
た樹脂組成物は射出成形品の表面平滑性が著しく劣って
おり、ランプリフレクター用としては使用不可であっ
た。
Comparative Example 2 Glass fiber and calcium carbonate were mixed in amounts of 20 and 20, respectively.
Melt kneading, injection molding and property evaluation were carried out in exactly the same manner as in Example 1 except that the amount was 40% by weight. The resin composition obtained here was extremely inferior in the surface smoothness of the injection-molded product, and could not be used for a lamp reflector.

【0029】実施例2〜8 PPS樹脂、PPO樹脂、ガラス繊維および無機充填材
の種類および配合比を表2に示すように種々変えて実施
例1と同様に溶融混練、射出成形および所定の特性評価
を実施した。結果を表1にあわせて示した。ここで得ら
れた樹脂組成物およびその射出成形品はいずれも耐熱
性、強度、剛性、寸法安定性、成形加工性および表面平
滑性、金属蒸着膜密着性などの特性を満足するものであ
った。
Examples 2 to 8 As in Example 1, melt kneading, injection molding and predetermined characteristics were carried out by changing the types and compounding ratios of PPS resin, PPO resin, glass fiber and inorganic filler as shown in Table 2. An evaluation was carried out. The results are also shown in Table 1. The resin composition and its injection-molded article obtained here all satisfied the characteristics such as heat resistance, strength, rigidity, dimensional stability, moldability and surface smoothness, and metal vapor deposition film adhesion. .

【0030】[0030]

【表2】 [Table 2]

【0031】[0031]

【発明の効果】本発明のPPS樹脂組成物およびその成
形体は耐熱性、強度、剛性、寸法安定性、成形加工性お
よび表面平滑性、金属蒸着膜密着性などの特性を満足す
るものであり、これによりすぐれた自動車ランプリフレ
クター用材料を提供することが可能になった。
EFFECTS OF THE INVENTION The PPS resin composition of the present invention and the molded product thereof satisfy characteristics such as heat resistance, strength, rigidity, dimensional stability, moldability and surface smoothness, and adhesion of metal vapor deposition film. , Which makes it possible to provide excellent materials for automobile lamp reflectors.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 // B29K 71:00 81:00 ─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. 6 Identification number Office reference number FI technical display location // B29K 71:00 81:00

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】(A)ポリフェニレンスルフィド樹脂20
〜45重量%、(B)ポリフェニレンオキシド5〜30
重量%、(C)繊維径7μm以下の細径ガラス繊維0〜
15重量%および(D)非繊維状無機充填材25〜75
重量%からなる混合物を溶融混練することにより得るこ
とを特徴とする樹脂組成物。
1. A polyphenylene sulfide resin 20 (A).
~ 45% by weight, (B) polyphenylene oxide 5-30
% By weight, (C) small diameter glass fiber having a fiber diameter of 7 μm or less 0 to
15% by weight and (D) non-fibrous inorganic filler 25-75
A resin composition, which is obtained by melt-kneading a mixture consisting of wt%.
【請求項2】(A)ポリフェニレンスルフィド樹脂20
〜45重量%、(B)ポリフェニレンオキシド5〜30
重量%、(C)繊維径7μm以下の細径ガラス繊維0〜
15重量%および(D)非繊維状無機充填材25〜75
重量%からなる混合物を溶融混練して得られる樹脂組成
物を射出成形することにより得られる表面平滑性のすぐ
れた成形体。
2. A polyphenylene sulfide resin (A) 20.
~ 45% by weight, (B) polyphenylene oxide 5-30
% By weight, (C) small diameter glass fiber having a fiber diameter of 7 μm or less 0 to
15% by weight and (D) non-fibrous inorganic filler 25-75
A molded product having excellent surface smoothness, which is obtained by injection molding a resin composition obtained by melt-kneading a mixture of 1% by weight.
【請求項3】請求項2記載の成形体において、成形体が
ランプリフレクター用である請求項2記載の成形体。
3. The molded product according to claim 2, wherein the molded product is for a lamp reflector.
JP19980893A 1993-08-11 1993-08-11 Resin composition and molded article Expired - Fee Related JP3528208B2 (en)

Priority Applications (1)

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Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19980893A JP3528208B2 (en) 1993-08-11 1993-08-11 Resin composition and molded article

Publications (2)

Publication Number Publication Date
JPH0753865A true JPH0753865A (en) 1995-02-28
JP3528208B2 JP3528208B2 (en) 2004-05-17

Family

ID=16413983

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Link
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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999042758A1 (en) * 1998-02-20 1999-08-26 Nippon Zeon Co., Ltd. Lighting equipment
KR20000029411A (en) * 1998-10-29 2000-05-25 엔다 나오토 Polypenylene sulfide resin composite material
JP2011126973A (en) * 2009-12-16 2011-06-30 Tosoh Corp Polyarylene sulfide composition
WO2013099234A1 (en) 2011-12-28 2013-07-04 東レ株式会社 Polyphenylene sulfide resin composition, molded article of polyphenylene sulfide resin composition, and method for producing polyphenylene sulfide resin composition
US8492467B2 (en) 2009-05-22 2013-07-23 Asahi Kasei Chemicals Corporation Automotive lamp peripheral parts
US8895655B2 (en) 2010-11-24 2014-11-25 Asahi Kasei Chemicals Corporation Automotive lamp extension molding
WO2016084635A1 (en) * 2014-11-25 2016-06-02 アイシン精機株式会社 Damper apparatus
CN112679956A (en) * 2020-12-21 2021-04-20 东莞市华盈新材料有限公司 High-precision low-overflow low-warpage low-dielectric PPS modified material and preparation method thereof

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50156561A (en) * 1974-06-11 1975-12-17
JPH02222452A (en) * 1989-02-23 1990-09-05 Dainippon Ink & Chem Inc Resin composition
JPH02281788A (en) * 1989-04-24 1990-11-19 Mitsubishi Gas Chem Co Inc Laminated board for high frequency printed wiring board
JPH04202364A (en) * 1990-11-30 1992-07-23 Tosoh Corp Polyphenylene sulfide resin composition
JPH0559280A (en) * 1991-08-29 1993-03-09 Dainippon Ink & Chem Inc Resin composition
JPH05171043A (en) * 1991-12-25 1993-07-09 Tosoh Corp Polyphenylene sulfide resin composition
JPH05179133A (en) * 1991-12-27 1993-07-20 Nippon G Ii Plast Kk Resin composition
JPH05320506A (en) * 1992-05-26 1993-12-03 Dainippon Ink & Chem Inc Lamp reflector

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50156561A (en) * 1974-06-11 1975-12-17
JPH02222452A (en) * 1989-02-23 1990-09-05 Dainippon Ink & Chem Inc Resin composition
JPH02281788A (en) * 1989-04-24 1990-11-19 Mitsubishi Gas Chem Co Inc Laminated board for high frequency printed wiring board
JPH04202364A (en) * 1990-11-30 1992-07-23 Tosoh Corp Polyphenylene sulfide resin composition
JPH0559280A (en) * 1991-08-29 1993-03-09 Dainippon Ink & Chem Inc Resin composition
JPH05171043A (en) * 1991-12-25 1993-07-09 Tosoh Corp Polyphenylene sulfide resin composition
JPH05179133A (en) * 1991-12-27 1993-07-20 Nippon G Ii Plast Kk Resin composition
JPH05320506A (en) * 1992-05-26 1993-12-03 Dainippon Ink & Chem Inc Lamp reflector

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999042758A1 (en) * 1998-02-20 1999-08-26 Nippon Zeon Co., Ltd. Lighting equipment
US6883938B1 (en) 1998-02-20 2005-04-26 Nippon Zeon Co., Ltd. Lighting equipment
KR20000029411A (en) * 1998-10-29 2000-05-25 엔다 나오토 Polypenylene sulfide resin composite material
US8492467B2 (en) 2009-05-22 2013-07-23 Asahi Kasei Chemicals Corporation Automotive lamp peripheral parts
JP2011126973A (en) * 2009-12-16 2011-06-30 Tosoh Corp Polyarylene sulfide composition
US8895655B2 (en) 2010-11-24 2014-11-25 Asahi Kasei Chemicals Corporation Automotive lamp extension molding
WO2013099234A1 (en) 2011-12-28 2013-07-04 東レ株式会社 Polyphenylene sulfide resin composition, molded article of polyphenylene sulfide resin composition, and method for producing polyphenylene sulfide resin composition
US9187641B2 (en) 2011-12-28 2015-11-17 Toray Industries, Inc. Polyphenylene sulfide resin composition, molded product of polyphenylene sulfide resin composition and production method of polyphenylene sulfide resin composition
US9416272B2 (en) 2011-12-28 2016-08-16 Toray Industries, Inc. Polyphenylene sulfide resin composition, molded product of polyphenylene sulfide resin composition and production method of polyphenylene sulfide resin composition
WO2016084635A1 (en) * 2014-11-25 2016-06-02 アイシン精機株式会社 Damper apparatus
CN112679956A (en) * 2020-12-21 2021-04-20 东莞市华盈新材料有限公司 High-precision low-overflow low-warpage low-dielectric PPS modified material and preparation method thereof

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