JPH02112177A - Connector - Google Patents

Connector

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Publication number
JPH02112177A
JPH02112177A JP26472188A JP26472188A JPH02112177A JP H02112177 A JPH02112177 A JP H02112177A JP 26472188 A JP26472188 A JP 26472188A JP 26472188 A JP26472188 A JP 26472188A JP H02112177 A JPH02112177 A JP H02112177A
Authority
JP
Japan
Prior art keywords
connector
weight
resin
organopolysiloxane
molding
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
JP26472188A
Other languages
Japanese (ja)
Other versions
JPH0350390B2 (en
Inventor
Kazuyoshi Kubo
久保 和善
Takao Nozaki
隆男 野崎
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.)
Sumitomo Wiring Systems Ltd
Original Assignee
Sumitomo Wiring Systems 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 Sumitomo Wiring Systems Ltd filed Critical Sumitomo Wiring Systems Ltd
Priority to JP26472188A priority Critical patent/JPH02112177A/en
Publication of JPH02112177A publication Critical patent/JPH02112177A/en
Publication of JPH0350390B2 publication Critical patent/JPH0350390B2/ja
Granted legal-status Critical Current

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  • Organic Insulating Materials (AREA)
  • Injection Moulding Of Plastics Or The Like (AREA)
  • Connector Housings Or Holding Contact Members (AREA)

Abstract

PURPOSE:To improve productivity of a connector by composing a component material thereof of the component of polybutyleneterephtharate resin of specific maximum viscosity including filler of silica, metallic salt of fatty acid and organopolysiloxane or its compound. CONSTITUTION:A component material of a connector is composed of polybutyleneterephtharate resin of maximum viscosity of 0.60 to 1.50dl/g including filler of silica, metallic salt of fatty acid and organopolysiloxane or its compound. Brending ratio of the filler of silica, metallic salt of fatty acid and the organopolysiloxane or its compound are 0.01 to 3.00wt.%, respectively. These component are molded by injection molding to form a connector. Accordingly, solidification of melted resin in a molding die is accelerated. Further, the resin thus solidified in the molding die is easily picked up therefrom. Thus, molding cycle is shortened, so that productivity is improved.

Description

【発明の詳細な説明】 (産業上の利用分野) この発明は、例えば自動車用の電気・電子機器回路を接
続するためのポリブチレンチレフタレ−1〜(以下rP
BTJと称す)樹脂製のコネクターに関する。
Detailed Description of the Invention (Industrial Field of Application) The present invention relates to polybutylene lenticules 1 to 1 (hereinafter referred to as rP
This invention relates to a resin connector (referred to as BTJ).

(従来の技術とその課題) 射出成形により得られるプラスブックコネクターの中で
PBT樹脂製のものは、耐熱変形性、i4薬品性、1法
安定性に優れるため、今後の使用量は著しく伸長するも
のと考えられている。特に自動車ワイヤハーネス用コネ
クターの場合、その材料どして以前からのポリ)7ミド
等の他材料から、上記高性能なPBT樹脂への置換が著
しく進むものと思われる。一方、自動車用コネクターは
、要求される機能の増加にともなう形状の複雑化、ざら
にコス]・ダウンおにび軽量化を目的とした薄肉化等が
要求されるが、それらの要求にも増して、特に生産性の
向上が強く要求されている。
(Conventional technology and its issues) Among the plus book connectors obtained by injection molding, those made of PBT resin have excellent heat deformation resistance, i4 chemical resistance, and method 1 stability, so their usage will increase significantly in the future. It is considered a thing. Particularly in the case of connectors for automobile wire harnesses, it is thought that the replacement of other materials such as poly)7mide, which have been used in the past, with the above-mentioned high-performance PBT resin will progress significantly. On the other hand, connectors for automobiles are required to have more complex shapes due to the increase in required functions, thinner walls for the purpose of reducing cost and weight. Therefore, there is a strong demand for improved productivity.

しかしながら、従来のPBT樹脂製]ネクタでは、射出
成形時における金型内での溶融樹脂の固化速度が遅いと
ともに、金型からの離型性能にも劣っており、成形サイ
クルが艮くなり上述の生産性向上に対処できないという
問題があった。
However, with conventional PBT resin connectors, the solidification rate of the molten resin in the mold during injection molding is slow, and the mold release performance from the mold is also poor, making the molding cycle difficult and causing the above-mentioned problems. The problem was that it was not possible to improve productivity.

(発明の目的) この発明は、上記従来技術の問題を解消し、生産性に優
れたコネクターを提供することを目的どする。
(Object of the Invention) An object of the present invention is to solve the problems of the prior art described above and provide a connector with excellent productivity.

(目的を達成Jるための手段) 上記目的を達成するため、この発明の−」ネクタは、シ
リカ系フィラーが001〜300161%、脂肪酸の金
属塩が001〜300重量%およびオルガノポリシロキ
サンまたはAルノjノポリシ1111ノン化合物が00
1〜3,00弔吊%含石され/j極限粘度数0.60〜
1.50dj!/!?のボリブyレンチレフタレー1〜
m脂組成物により構成している。
(Means for Achieving the Object) In order to achieve the above object, the nectar of the present invention contains 001 to 300161% by weight of a silica filler, 001 to 300% by weight of a metal salt of a fatty acid, and an organopolysiloxane or A Runo J Nopolicy 1111 Non Compound 00
Contains 1 to 3,00% stone/j Intrinsic viscosity 0.60 to
1.50dj! /! ? Voliv Y Wrench Leftare 1~
It is composed of m-fat composition.

(実流例) この発明の一実施例である」ネクターは、シリカ系フィ
ラーが001〜3.00ヰ吊%、脂肪酸の金属塩が0.
01〜300重量%およびオルガノポリシロキサンまた
はオルガノポリシ[1キリン化合物が0.01〜3.0
0Φ量%含イjされた極限粘頂数0.60〜1.50d
1/gのポリエチレンテレフタレート(以下rPB王」
と称す)樹脂組成物にJ、り構成され、その組成物を割
出成形d、にJ、り成形してコネクターとして製品化す
る。
(Example of Actual Flow) Nectar, which is an embodiment of the present invention, has a silica filler of 0.01 to 3.00% and a fatty acid metal salt of 0.00%.
01 to 300% by weight and organopolysiloxane or organopolysiloxane [1 Kirin compound is 0.01 to 3.0% by weight]
Limiting viscosity peak number 0.60 to 1.50d containing 0Φ amount%
1/g polyethylene terephthalate (rPB king)
The connector is made of a resin composition (referred to as ``J''), and the composition is molded by index molding to produce a connector.

上記組成物は、則111成形時における金型内(−の溶
融樹脂の段階で同化速度が速く、溶融樹脂の冷却時間が
大幅に短縮されるとともに、固化した後金型材質との密
肴性が低く離型性に優れ、成形サイクルが短縮されて=
1ネクターの生産性が向上する。
The above composition has a high assimilation rate at the stage of molten resin in the mold (-) during molding according to Rule 111, significantly shortens the cooling time of the molten resin, and has good adhesion with the mold material after solidification. Low mold releasability, shortened molding cycle =
1 nectar productivity improves.

次に、各構成要素を例示的に説明する。Next, each component will be exemplarily explained.

まず、P[31−樹脂(,1、例えば1./I−ブタン
ジオールとジメチルjレノタレ−1−から製造されるも
のが用いられるが、代りに製造の際に必要に応じて]−
チレングリコール、1.3−プロパンジオール雪のジオ
ールや、−jレノクル酸以外のジカルボン酸などの少量
の第三成分を共縮合させたポリマーを用いてもJ:い。
First, P[31-resin (,1, for example, one produced from 1./I-butanediol and dimethyl j-renotare-1- is used, but instead, if necessary during production]-
A polymer co-condensed with a small amount of a third component such as ethylene glycol, 1,3-propanediol, or dicarboxylic acid other than -jlenocric acid may also be used.

この実流例Cは、テ1〜ラク[1ル]−タン/フェノー
ルの/10/60(重量%)混合溶媒中、30°Cての
極限粘度数[η]が060・〜1.50d、f!/Jの
P F3 T樹脂が用いられる。
This actual flow example C has an intrinsic viscosity [η] of 060 to 1.50 d at 30°C in a /10/60 (wt%) mixed solvent of Te1~lac[1ru]-tane/phenol. , f! /J P F3 T resin is used.

極限粘度数「η1は1記範囲内であればよいが、特に 
07()−・140(jj!/!7の範囲内であればよ
り好ましくなる。なa′3、極限粘度数[η]が060
d1/!?以下の揚台には組成物の機械的強度が著しく
低下して」ネクターの強度が低1;づ−るー・方、1.
50 (l i /シ以トの場合には流動性が低小して
溶融樹脂が金型内へスムースに充填されず不完全充填等
が発生し、割出成形が困難となる。
The intrinsic viscosity number "η1" may be within the range listed in 1, but in particular
It is more preferable if it is within the range of 07()-・140(jj!/!7.A′3, the intrinsic viscosity number [η] is 060
d1/! ? On the following platforms, the mechanical strength of the composition is significantly reduced and the strength of the nectar is low.
In the case of less than 50 (l i /sheet), the fluidity is so low that the molten resin cannot be smoothly filled into the mold, resulting in incomplete filling and the like, making index molding difficult.

シリカ系フィラーとしては、シリカ、シリカ・アルミナ
、ガラス粉またはガラスピーズ、タルク。
Silica-based fillers include silica, silica/alumina, glass powder or glass peas, and talc.

ケイソウ士、クレー、マイカ、シラス等が例示される。Examples include diatom, clay, mica, and whitebait.

その添加量は、0.01〜3.00重量%の範囲内であ
ればよく、特に002・〜1,00重川%の範囲内であ
ればより好ましくなる。なお、001重量%以下では、
成形サイクルの短縮が図れず1−産性に劣る一方、3.
00重量%以上では得られるコネクターの1Jvji撃
牲が低下して好ましくない1゜脂肪酸の金属塩としては
、飽和または不飽和脂肪酸のナトリウム、カリウム、ベ
リリウム、マグネシウム、カルシウム、リヂウム、アル
ミニーシム。
The amount added may be within the range of 0.01 to 3.00% by weight, and more preferably within the range of 0.02 to 1,00% by weight. In addition, at 001% by weight or less,
The molding cycle cannot be shortened, resulting in poor productivity; 3.
Examples of metal salts of 1° fatty acids, which are undesirable since the 1JvJI impact strength of the resulting connector is lowered by 00% by weight or more, include saturated or unsaturated fatty acids such as sodium, potassium, beryllium, magnesium, calcium, lithium, and aluminum shim.

鉛、亜鉛等の塩が例示され、その中でも特にステアリン
酸の塩が好ましく、例えば、ステアリン酸カルシウム、
ステアリン酸カルシウム、ステアリン酸亜鉛等を挙げる
ことができる。脂肪酸の金属塩の配合量としては、00
1・〜3.00重量%の範囲内であればよく、特に0.
02−、1.00小量%の範囲内であればより好ましい
。なお0.01重量%以下では生産性に劣る一方、30
0重量%以上では−」ネクターの機械的強度が低下した
り、]ネクター表面に脂肪酸の金属塩が移行くブリード
現象)したりして好ましくない。
Salts of lead, zinc, etc. are exemplified, and among these, salts of stearic acid are particularly preferred, such as calcium stearate,
Examples include calcium stearate and zinc stearate. The blending amount of fatty acid metal salt is 00
It may be within the range of 1. to 3.00% by weight, especially 0.00% by weight.
It is more preferable if it is within the range of 0.02-, 1.00%. Note that below 0.01% by weight, productivity is poor;
If it is more than 0% by weight, it is not preferable because the mechanical strength of the nectar decreases or a bleeding phenomenon occurs in which metal salts of fatty acids migrate to the surface of the nectar.

オルガノポリシ[11−リーンとしては、一般に撥水剤
、消泡剤、離を剤、潤滑剤、シール剤などの各種の応用
に使用されているΔルガノボリシロキサンオイルであり
、最も一般的なジメブルシリコーン、あるいはこのりか
にメヂル基の一部を水素、)]ニル基イの他の反応性の
ない有機基あるいは、]7ポー1シ基 ノ′ミノ基、ビ
ニル基、(メタ)アクリル基などの官能性の石m基をも
つΔルガノポリシロキ1ノンし含まれる。
Organopolysiloxane oil is generally used in various applications such as water repellents, antifoaming agents, release agents, lubricants, and sealants, and is the most common Hydrogen or other non-reactive organic groups such as hydrogen, )]nyl group, or ]7-polysilicone, or amino group, vinyl group, (meth)acrylic group It includes Δluganopolysiloquinone with functional stone groups such as.

その化合物、つまりオルガノポリシロ4−ザン化合物ど
じでは、ジメヂルポリシ1l−1−(JンジA−ル。
The compound, ie, the organopolysilyl 4-zan compound, is dimethylpolysil.

メヂルフエニルポリシロニIIナンジオール、ジフェニ
ルポリシロキザンジオールのように末端に水酸基を右J
るAルカノボリシロキリン類:メヂルハイドロジ丁ンポ
リシロ1ニリン、ジメチルボリシロキサンメチルハイド
ロジエンポリシロキサン共縮合物のようにケイ素原子に
直結する水素を有するオルガノポリシロキサン類;ジフ
ェニルポリシロキサン、ジメヂルシロキザン、メブルフ
ェニルポリシロキサン、エポキシ変性ジメチルシロキサ
ン。
Right J
A-kanoborisiloxanes: organopolysiloxanes having hydrogen directly bonded to silicon atoms such as methylhydrodidine polysiloxane, dimethylborisiloxane methylhydrodiene polysiloxane cocondensates; diphenylpolysiloxane, dimylsiloxane, Mebruphenylpolysiloxane, epoxy-modified dimethylsiloxane.

アミノ変性シロキサン等を挙げることができる。Examples include amino-modified siloxane.

オルガノポリシロ1サンまたはでの化合物の配合量とし
ては、0.01〜3.00重量%の範囲内であればよく
、特に0.02〜1,00重量%の範囲内であればより
好ましい。なお、001重量%以下では生産性に劣る一
方、3.00重量%以上ではコネクターの機械的強電、
特につ1ルド強度が低下して好ましくない。
The compounding amount of the compound in organopolysilone 1 may be within the range of 0.01 to 3.00% by weight, and more preferably within the range of 0.02 to 1,00% by weight. . In addition, if it is less than 0.001% by weight, the productivity will be poor, while if it is more than 3.00% by weight, the mechanical power of the connector will be reduced.
In particular, it is undesirable because the twist strength decreases.

また、上記材料により構成される組成物においては、必
要に応じて、ガラス繊維、炭素繊維等の繊維状強化剤を
使用することによって剛t’1.Wの向上を図ることが
できる。他に、核剤、l1llt型剤、カップリング剤
9着色剤、滑剤、耐熱安定剤、耐候安定剤、難燃剤、難
燃助剤、可塑剤等を添加してもよい。
In addition, in the composition made of the above-mentioned materials, the stiffness t'1. W can be improved. In addition, a nucleating agent, a l1llt type agent, a coupling agent, a coloring agent, a lubricant, a heat stabilizer, a weather stabilizer, a flame retardant, a flame retardant aid, a plasticizer, etc. may be added.

さらに、必要に応じて、ポリエチレンテレフタシー1〜
.ポリアミド、ウレタン化PBT、ポリエチレン、ポリ
プロピレン、ポリスチレン、ポリアクリレート、ABS
、AS、ポリ塩化ビニル、ポリアセタール、ポリカーボ
ネート、ポリサルホンポリエーテルサルホン、ポリフェ
ニレンオキシド。
Furthermore, if necessary, polyethylene terephthalate 1 to
.. Polyamide, urethanized PBT, polyethylene, polypropylene, polystyrene, polyacrylate, ABS
, AS, polyvinyl chloride, polyacetal, polycarbonate, polysulfone polyether sulfone, polyphenylene oxide.

ポリフェニレンサルファイド等のプラスチック類やポリ
エステル系、ポリアミド系、ポリウレタン系、アクリル
系、オレフィン系、塩化ビニル系。
Plastics such as polyphenylene sulfide, polyester, polyamide, polyurethane, acrylic, olefin, and vinyl chloride.

スヂレン系、ABS系等の熱可塑性■ラストマー類を添
加することも可能ぐある。
It is also possible to add thermoplastic lastomers such as styrene and ABS.

なお1、組成物の調製は種々の公知の方法で可能である
。例えば、原石を予めタンブラ−又はヘンシエルミキザ
ーのような混合機で均一に混合した後、−軸又は二軸の
押出機等に供給して溶融混練した後、ペレット状の組成
物として調製する方法等がある。
Note that the composition can be prepared by various known methods. For example, raw stones are mixed uniformly in advance using a mixer such as a tumbler or Henschel mixer, and then fed into a -screw or twin-screw extruder, where they are melted and kneaded, and then prepared as a pellet-like composition. There are methods etc.

また、組成物の成形方法は、通常の射出成形機により行
なえ、好ましくは射出成形機の設定温度として、シリン
ダー230〜290℃、金型10〜80℃の範囲内がよ
い。
Further, the composition can be molded using a common injection molding machine, and preferably the set temperature of the injection molding machine is within the range of 230 to 290°C for the cylinder and 10 to 80°C for the mold.

次に、この発明を実験例により具体的に説明する。ここ
では、この発明に基づく実験例1〜/Iと、この発明の
構成要素を満足しない比較例1〜4とを行ない、両者を
比較することによりこの発明の詳細な説明する。言うま
でもないが、この発明は、以下に示す実験例1〜4に限
定されるものではない。
Next, this invention will be specifically explained using experimental examples. Here, Experimental Examples 1 to /I based on the present invention and Comparative Examples 1 to 4 that do not satisfy the constituent elements of the present invention will be conducted, and the present invention will be explained in detail by comparing the two. Needless to say, the present invention is not limited to Experimental Examples 1 to 4 shown below.

なお、例中の部は重量部を意味する。Note that parts in the examples mean parts by weight.

実験例1 テトラクロルJタン/フ1゛ノールΦ40/60(重量
%)の混合溶媒中で測定した極限粘度数[η1が0.9
2 d 1 / g、のPBT樹脂99,3部、脂肪酸
の金属塩としてモンタンワックスエステルカルシウム塩
0.3部(0,30重量%)、シリカ系フィラーとして
タルク0.2部(0,20重間%)、オルガノポリシロ
キサンとしてPS−043(チッソ株式会社製オルガノ
ポリシロキサン 粘度1,000c t s k ) 
 0.2部(0,20重量%)を均一混合した後、40
mφ−軸押出機を用いて240’Cのシリンダー温度で
溶融混練し、ペレット状の組成物に調製しICoその後
、得られたペレット状の組成物を使用して、10オンス
のスクリュー型射出成形機によりシリンダー温度260
℃、金型温度45℃9割出圧1,400〜5QOK9/
af+、射出速度中速の成形条件で、図面に示されるよ
うな自動車ワイヤハーネス用コネクター1を、そのコネ
クター1が一度に8個型取りできるいわゆる8個取り金
型にて成形した。そして、外観良好なコネクター1が連
続的に得られる場合の最短の成形サイクル(秒)を測定
した。
Experimental Example 1 Intrinsic viscosity [η1 is 0.9] measured in a mixed solvent of tetrachlor J tan/phenol Φ40/60 (wt%)
2 d 1 / g, PBT resin 99.3 parts, montan wax ester calcium salt 0.3 part (0.30% by weight) as a fatty acid metal salt, talc 0.2 part (0.20% by weight) as a silica filler. PS-043 (Organopolysiloxane manufactured by Chisso Corporation, viscosity 1,000ctsk), as organopolysiloxane
After uniformly mixing 0.2 parts (0.20% by weight), 40
The pelletized composition was prepared by melt-kneading using an mφ-screw extruder at a cylinder temperature of 240'C, and the resulting pelletized composition was then molded into a 10-ounce screw type injection molding. Cylinder temperature 260 depending on the machine
℃, mold temperature 45℃ 9 indexing pressure 1,400~5QOK9/
Under molding conditions of af+ and medium injection speed, a connector 1 for an automobile wire harness as shown in the drawing was molded using a so-called 8-cavity mold capable of molding 8 connectors 1 at a time. Then, the shortest molding cycle (seconds) in which connectors 1 with good appearance could be continuously obtained was measured.

実験例2 実験例1のモンタンワックスエステルカルシウム塩0.
3部に代えてステアリン酸マグネシウム03部を用いた
ことを除ぎ、実験例1と全く同様に成形し、同様の評価
を行なった。
Experimental Example 2 Montan wax ester calcium salt of Experimental Example 1 0.
It was molded in exactly the same manner as in Experimental Example 1, except that 0.3 parts of magnesium stearate was used instead of 3 parts, and the same evaluation was performed.

実験例3 実験例1のタルク02部に代えてマイカ02部(020
重量%)を用いたことを除き、実験例1と全く同様に成
形し、同様の評価を行なった。
Experimental Example 3 In place of 02 parts of talc in Experimental Example 1, 02 parts of mica (020
The molding was performed in exactly the same manner as in Experimental Example 1, except that % by weight) was used, and the same evaluation was performed.

実験例4 実験例1のPS−0430,2部に代えでPS045(
チッソ株式会社製オルガノポリシ[11ニリ−ン 粘度
10,0OOc t s k )を用いたことを除き、
実験例1と全く同様に成形し、同様の評価を行イγつだ
Experimental Example 4 PS045 (
Except for using Chisso Corporation's organopolis [11 nirene, viscosity 10.0OOc tsk)]
It was molded in exactly the same manner as in Experimental Example 1 and evaluated in the same manner.

比較例1 実験例1のモンタンワックス]ニスチルカルシウム塩を
用いなかったことを除き、実験例1と全く同様に成形し
、同様の評価を行なった。
Comparative Example 1 Montan wax of Experimental Example 1] It was molded in exactly the same manner as in Experimental Example 1, except that the Nistil calcium salt was not used, and the same evaluation was performed.

比較例2 実験例1のタルクを用いなかったことを除さ、実験例1
と全く同様に成形し、同様の評価を11なった。
Comparative Example 2 Experimental Example 1 except that talc of Experimental Example 1 was not used.
It was molded in exactly the same manner as above and received a similar evaluation of 11.

比較例3 実験例1のl” S−043を用いなかったことを除き
、実験例1と全く同様に成形し、同様の評価を行なった
Comparative Example 3 The molding was performed in exactly the same manner as in Experimental Example 1, except that the l'' S-043 of Experimental Example 1 was not used, and the same evaluation was performed.

比較例4 実験例1のモンタンワックスTステルカルシウム塩、タ
ルク及びP S 、−、043を用いイヱかったことを
除いて実験例1と全く同様に成形し、同様の評価を行な
った。
Comparative Example 4 Molding was performed in exactly the same manner as in Experimental Example 1, except that Montanwax T Stell calcium salt, talc, and P S ,-,043 of Experimental Example 1 were used, and the same evaluation was performed.

それぞれの結果を表1に示J。The results are shown in Table 1.

表  1 表1に示されるように、実験例1へ・4ではその成形4
ノイクルが25〜30秒と短面間であるのに対し、比較
例1・〜4で4.L 40−60秒と長時間であり、実
験例1〜・4は生産性に優れることが判明し lこ 。
Table 1 As shown in Table 1, in Experimental Examples 1 and 4, the molding 4
While Noikle was short between 25 and 30 seconds, Comparative Examples 1 to 4 were 4. It took a long time, 40-60 seconds, and it was found that Experimental Examples 1 to 4 had excellent productivity.

(発明の効果) 以上のように、この発明のコネクターによれば、射出成
形時における溶融樹脂の金型内での固化速度が速くなる
とともに、固化した後金型との離型性が良好となるので
、成形ザイクルが短くなり1産性に優れるという効果が
1qられる、1
(Effects of the Invention) As described above, according to the connector of the present invention, the solidification speed of the molten resin in the mold during injection molding is increased, and the mold releasability from the mold after solidification is improved. Therefore, the effect of shortening the molding cycle and improving productivity is increased by 1q, 1

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

図面はこの発明に基づく実験例により1qられた自動型
ワイヤハーネス用」ネクターを示す斜視図である。 1・・・]コネク タ理人 弁理士 吉田茂明
The drawing is a perspective view showing a 1Q connector for an automatic wire harness according to an experimental example based on the present invention. 1...] Connector Attorney Patent Attorney Shigeaki Yoshida

Claims (1)

【特許請求の範囲】[Claims] (1)シリカ系フィラーが0.01〜3.00重量%、
脂肪酸の金属塩が0.01〜3.00重量%およびオル
ガノポリシロキサンまたはオルガノポリシロキサン化合
物が0.01〜3.00重量%含有された極限粘度数0
.60〜1.50dl/gのポリブチレンテレフタレー
ト樹脂組成物により構成したことを特徴とするコネクタ
ー。
(1) Silica filler is 0.01 to 3.00% by weight,
Intrinsic viscosity number 0 containing 0.01 to 3.00% by weight of a metal salt of a fatty acid and 0.01 to 3.00% by weight of an organopolysiloxane or an organopolysiloxane compound.
.. A connector comprising a polybutylene terephthalate resin composition of 60 to 1.50 dl/g.
JP26472188A 1988-10-20 1988-10-20 Connector Granted JPH02112177A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP26472188A JPH02112177A (en) 1988-10-20 1988-10-20 Connector

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP26472188A JPH02112177A (en) 1988-10-20 1988-10-20 Connector

Publications (2)

Publication Number Publication Date
JPH02112177A true JPH02112177A (en) 1990-04-24
JPH0350390B2 JPH0350390B2 (en) 1991-08-01

Family

ID=17407260

Family Applications (1)

Application Number Title Priority Date Filing Date
JP26472188A Granted JPH02112177A (en) 1988-10-20 1988-10-20 Connector

Country Status (1)

Country Link
JP (1) JPH02112177A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5502119A (en) * 1992-12-03 1996-03-26 General Electric Company Stabilized polyester-polycarbonate compositions

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5502119A (en) * 1992-12-03 1996-03-26 General Electric Company Stabilized polyester-polycarbonate compositions

Also Published As

Publication number Publication date
JPH0350390B2 (en) 1991-08-01

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