JPS5865643A - Silicone rubber molded body and manufacture thereof - Google Patents

Silicone rubber molded body and manufacture thereof

Info

Publication number
JPS5865643A
JPS5865643A JP16462581A JP16462581A JPS5865643A JP S5865643 A JPS5865643 A JP S5865643A JP 16462581 A JP16462581 A JP 16462581A JP 16462581 A JP16462581 A JP 16462581A JP S5865643 A JPS5865643 A JP S5865643A
Authority
JP
Japan
Prior art keywords
curing catalyst
composition
component
silicone rubber
curing
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
JP16462581A
Other languages
Japanese (ja)
Other versions
JPH028582B2 (en
Inventor
Ryoichi Sado
佐渡 良一
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.)
Shin Etsu Polymer Co Ltd
Shin Etsu Chemical Co Ltd
Original Assignee
Shin Etsu Polymer Co Ltd
Shin Etsu Chemical Co 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 Shin Etsu Polymer Co Ltd, Shin Etsu Chemical Co Ltd filed Critical Shin Etsu Polymer Co Ltd
Priority to JP16462581A priority Critical patent/JPS5865643A/en
Publication of JPS5865643A publication Critical patent/JPS5865643A/en
Publication of JPH028582B2 publication Critical patent/JPH028582B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Insulating Bodies (AREA)
  • Laminated Bodies (AREA)
  • Heating, Cooling, Or Curing Plastics Or The Like In General (AREA)
  • Lining Or Joining Of Plastics Or The Like (AREA)
  • Organic Insulating Materials (AREA)

Abstract

PURPOSE:To produce efficiently a molded item, by bringing a diorganopolysiloxane composition that will not crosslink into surface contact with an organopolysiloxane composition that contains a curing catalyst which can initiate the crosslinking reaction of the former composition. CONSTITUTION:A fluid organopolysiloxane that contains an electrical conductivity giving agent but does not contain a curing catalyst is cast to a part of a cavity of a mold where a contact it to be formed, and then an insulating organopolysiloxane composition that contains a curing catalyst is cast thereonto. Then the mold is heated to cure the compositions to obtain a pushing button switch cover molded body having an electrically conductive contact.

Description

【発明の詳細な説明】 本発明はりツフーンゴム成形体、特痕二は電子機器部品
として有用なりリコーン成形体およびその製造方法に関
するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a silicone molded product useful as an electronic device component and a method for producing the same.

シリコーンゴム成形体は、一般にジオルガノボ9VOキ
チンを主体ど1丁ゐオルガノポリシaキサシ組成物C二
必要量の硬化触媒1例えば有機過酸化物、金−有機酸塩
あるいにエステル、アミン化合物、$4級アyそニウム
塩、白金tたは白金化合物などを均一に分散混合したの
ち、これらを加温、加熱tたは加圧加熱T1=、あるい
は室温下で架橋反応させ、成形硬化させるという方法で
作られている。しかし仁の硬化触媒を含むオルガノポU
Vaキチン組成物の加硫的1itt−ディスク式レオメ
ータ−でみると、これは七の1硫時間の経過と共(:ト
ルクが上昇するものであ13.事実、圧秘成形、射出成
形など1:おけるオルガノボリシE7+fン組成物は架
橋反応の過渡状態で流動が起り、これC二よって金やキ
ャビティにそれが流入して成形体が得られるのであるか
ら、ここ−二得られるシリコーンゴム成形体4=は上記
過渡状態での加圧、圧縮による歪みや厚さのバラツキが
生じd<、1,7がってこの方法による極薄物や精密部
品の成形は歩留りがよくないという欠点がある。
The silicone rubber molded article is generally made of diorganocarbon 9VO chitin, an organopolymer composition C, and a necessary amount of a curing catalyst, such as an organic peroxide, a gold-organic acid salt or ester, an amine compound, $ After uniformly dispersing and mixing the quaternary asonium salt, platinum or platinum compound, etc., they are heated, heated at T1, pressure heated at T1=, or subjected to a crosslinking reaction at room temperature, and molded and hardened. made by the method. However, the organopolymer containing the curing catalyst
When looking at the vulcanization of Va chitin composition using a 1itt-disc rheometer, this shows that the torque increases with the passage of time (13. In fact, compression molding, injection molding, etc. The organoboric composition E7+f in the composition flows during the transient state of the crosslinking reaction, and it flows into the gold and the cavity to obtain a molded product. = causes distortion and variation in thickness due to pressure and compression in the above-mentioned transient state, d<, 1,7 Therefore, molding of ultra-thin objects and precision parts by this method has the disadvantage that the yield is poor.

tた、この成形法区二よる不利を少なくするため1:、
室温で流11性を示す硬化触媒を含むオルガノポリシロ
キチン組成物を室温付近でを内5:注入し1成形すると
いう方法も知られているが、この組成物−1硬化触媒温
合後のポットライフが短刀為く、デッドスペースでのゲ
ル化が起り易いという欠点があるほか、この場合C:は
硬化触媒の配合時に組成物中1:混式された気Sを予じ
め脱気しておく必要があ・」、これには1またその配合
用の容器、配普など&=ニゲル硬化物が残存しないよう
にそれらtひんばん一:洗浄しなければならないという
不利もある。
In order to reduce the disadvantages caused by this molding method, 1:
A method is also known in which an organopolysilochitin composition containing a curing catalyst exhibiting flowability at room temperature is injected at around room temperature and molded. In addition to shortcomings such as short pot life and easy gelation in dead spaces, in this case, C: is used by degassing air S mixed in 1: in the composition in advance when blending the curing catalyst. This also has the disadvantage that the containers for its formulation, distribution, etc. must be thoroughly washed to ensure that no cured product remains.

ナオ、各櫓の電子機am品1例えばインターコネクター
などの接点部材としてのシリコーンゴム成形品の成形シ
一ついては、予じめ成形した導電性ゴム部材と絶−性部
材とfWIIHIさせて一体成形品とする仁とが行なわ
れているが、これ(二ついては両部材の境界面で発生す
る気泡の除去か困難でああほか、両龜何がその境界面で
剥離し易いという欠点かある。そのため1本発8月者ら
はさき5ニー゛方のVリコーンゴム成分1:33 Ko
al/ mol a上の活性化エネルギーをもつ有機過
酸化物を配合し、これを他の一次成形品と共C二金染中
5二充填してW圧加熱するという方法全提案した(特開
昭5O−zoso参蕉)が、この場合5二は一次成形品
と二次成形品との間5二熱履歴や圧縮成形特の加圧によ
る歪みが発生し晶<、これ−二よって二次成形品に部分
的な変形が生じるほか、この−次成形品が導電性ゴムで
作られている場合1二はその表面に汚染が生じて導通不
良となったり、−次成形品の曾〜中での移動によって二
次成型品C二導通不良や短絡が発生するという不利があ
った◎ 本発明はこのような不利を解決しにvリフーン成形品お
よびその製造方法I:闘するものであり、これはそれ自
体だけでは架橋反応しないジオルガノボッシロキチン組
成物とこの組成物区二架檜反応を起させる硬化触媒また
はこの硬化触媒を含むオルガノポリシロキチン組成物と
の界面僧触で両者を一体成形品としてなることを特徴と
するものである。
Nao, electronic equipment AM products for each tower 1 For example, the molding process of silicone rubber molded products as contact members such as interconnectors is an integrally molded product made by fWIIHI with a pre-molded conductive rubber member and an insulating member. However, this method has two drawbacks: it is difficult to remove air bubbles that occur at the interface between the two parts, and the two parts tend to separate at the interface. The V silicone rubber component on the 5th knee side is 1:33 Ko.
A complete method was proposed in which an organic peroxide with an activation energy above al/mol a was blended, and this was filled with other primary molded products in a C dikin dyeing medium and heated under W pressure. In this case, distortion occurs between the primary molded product and the secondary molded product due to heat history and pressure applied during compression molding. In addition to partial deformation of the molded product, if the next molded product is made of conductive rubber, contamination may occur on its surface, resulting in poor conductivity, or damage to the middle of the next molded product. There was a disadvantage that secondary molded product C2 conduction defects and short circuits occurred due to movement of the secondary molded product C2.The present invention aims to solve these disadvantages by combating the following problems: This is achieved by interfacial contact between a diorganobossilochitin composition that does not undergo a crosslinking reaction by itself and a curing catalyst that causes a crosslinking reaction in this composition, or an organopolysilochitin composition containing this curing catalyst. It is characterized by being formed as an integrally molded product.

これ管説明すると、本発明看12 V 9コーンゴム製
の各検電子機!!部材の製造方法について種々検討の結
果、硬化触媒を含有せず、したがってそれ自体だけでは
架橋反応しないジオルガノポツリロキサンから作った賦
形体と、硬化触媒を含むジオルガノポUVaキサシ組成
物の賦形体でまだ完全感ニー化していない、したかって
まだ鹸化触媒機能を保有している賦形体と??l触させ
てこれらを加熱したところ、この後看i:含まれている
硬化触媒によって硬化触媒管含有していないシリコーン
ゴム賦形体もその指触界面から徐々I:硬化されるとい
うことを見出し、これ−二ついてさら(:゛実験を進め
た結果、硬化触媒を含まないジオルガノボッシロキチン
組成物の賦形体C:硬化触媒を界面接触させるか、この
硬化触媒を含むオルガノポリシロキチン組成物またはそ
の賦形体を界面接触させれば、この硬化触媒1含まない
ジオルガノボリシaキサン組成@−二架橋反応が進行し
、これは加熱硬化型。
To explain this tube, each inspection machine made of 12 V 9 cone rubber of the present invention! ! As a result of various studies on methods of manufacturing the parts, we found that we could use a molded body made from diorganopotulyloxane, which does not contain a curing catalyst and therefore does not undergo crosslinking reactions by itself, and a molded body of a diorganopolyxane composition that contains a curing catalyst. Is it an excipient that has not yet been fully sensitized, or even still retains saponification catalytic function? ? When they were heated by touching them, they found that the silicone rubber excipients that did not contain a curing catalyst tube were gradually cured from the touch interface by the curing catalyst contained therein. These are two of them (:゛As a result of the experiment, excipient C of a diorganobossilochitin composition that does not contain a curing catalyst: A curing catalyst is brought into interfacial contact, or an organopolysilochitin composition containing this curing catalyst Alternatively, if the excipient is brought into interfacial contact, this diorganoborisilaxane composition @-2 crosslinking reaction that does not contain curing catalyst 1 proceeds, and this is a heat-curing type.

宸温硬化金のいずれ6二ついても同様g二観察されるこ
とviPm認して本発明を完成させた。
The present invention was completed after recognizing that the same observation can be made in any case of warm hardening gold.

本発明i:使用されるオルガノポツシaキ夛ン組酸物は
従来公知のものでよく、これは例えば一般式Rn810
4−n  (c−にRは非麹換菫たは龜換の一価炭化水
素晶、nrx1.9〜2.1の正数)で示されるジオル
ガノボッシミキサνを主材とするもので、このRが主と
し七メチル基であり、これに必要に応じフェニル基、ビ
ニル基、アリル基、フaOプaビル基、Vアノプロピル
基などが尋人されたものであるが、これはまにその分子
細末端が水酸基、ビニル基、アリル−などの官能基で封
鎖されたものでもよい、このオルガノボラミ10キチン
の粘度は特C二これを規定する必要はないが。
Invention i: The organopolysium group acid used may be any conventionally known one, for example, one with the general formula Rn810
4-n (R in c- is non-koji-converted violet or koji-converted monovalent hydrocarbon crystal, nrx is a positive number of 1.9 to 2.1). , this R is mainly a 7-methyl group, and phenyl groups, vinyl groups, allyl groups, ao-p-a-vinyl groups, V-anopropyl groups, etc. are added to this as necessary, but this is not true. The fine end of the molecule may be capped with a functional group such as a hydroxyl group, a vinyl group, or an allyl group.The viscosity of this organoborami-10 chitin is not necessarily specified.

これは一般には28℃区二おける粘度が10〜2、00
 G、 0000pのものから任意に選択することがよ
く、これは通常too、oooop以上のもf)l二V
l力などの充填剤を添加した組成物として使用されるが
、これrstた酸化鉄などの耐熱性向上剤、各種の炭酸
塩、白金などの耐燃化剤、各植会鵬粉、カーボンブラッ
クなどの尋電性付今刑なのオルガノボッyaキ葉シ組成
物は硬化触媒の存在下で架橋反応が進行し、これ−二よ
って硬化物とサレるもので、これ−二ついては加熱硬化
型のものと常温−化型があるが1本発明のりリフーンゴ
ム成形品はこのいずれによっても作ゐことができる・な
お、この硬化触媒としては加熱硬化型、加圧加熱硬化型
のものについてに各種の有機過酸化物あるいは白金t1
eは白金化合物が、tだ常温硬化型のものC二ついては
その架橋反応のタイプC:よって相違するが、一般I:
ハ会−有機^しくはエステル、アミン化合物、184級
アンモニウム塩、白金またべ白金化合物などが例示され
、本発明においては仁のいずれもが使用される。
This generally has a viscosity of 10 to 2,000 at 28℃.
G, 0000p, which is usually too, oooop or more f)l2V
It is used as a composition with the addition of fillers such as iron oxide, heat resistance improvers such as iron oxide, various carbonates, flame retardants such as platinum, various powders, carbon black, etc. The cross-linking reaction of the organoboyaki leaf composition with the electric conductivity proceeds in the presence of a curing catalyst, and therefore it is a cured product, and these two are heat-curable. Although there is a room-temperature curing type, the glue refone rubber molded product of the present invention can be made using any of these methods.As for this curing catalyst, various organic peroxides can be used for the heat-curing type and pressurized heat-curing type. material or platinum t1
e is a platinum compound that cures at room temperature, and t is a type of crosslinking reaction.
Examples include organic compounds or esters, amine compounds, 184-grade ammonium salts, platinum compounds, and any of them can be used in the present invention.

本発明のi/1コーシゴム成形体の製造におけるll!
成分は、それ自体だけでは架橋反応しないジオルガノボ
9vaキナシM成物であり、これには加熱硬化薯のジオ
ルガノポ9VOキψy組酸物で有機過酸化物などの硬化
触媒を含有しないもの、またビニル基含有オルガノボリ
シaキtνと一81H晶を含むオルガノへイドaジェシ
ポリシaキ葉ンとを白金糸触媒の存在下で付加反応させ
るもの1=おける、ビニル基含有オルガノボリシロキサ
シ単独tたはこれ6二白金糸触媒を含有させたものなど
が例示されるが%これはまたいわゆる二液性常温硬化性
(R’l’V)組成物として公知のもので、この二液型
のうちの主剤だけのもの、*’lcこの二液型でA液と
B液とを当量配合するものについてはそのA液またはB
液のいずれか単独のものなどが例示される。そして、こ
れらのジオルガノポリシaキナyM酸物は室温で粘性流
動するか、室温で流動しない粘調体、あるい以りィリア
ム可塑度メーターで5oo以下の可塑度を示す粘弾性体
として使用されるが、このものはそれに架橋反応を起さ
せる硬化触媒またはこの硬化触媒を含む予じめ所望の形
状に賦形しておくことがよい、Cの賦形は例えば当該ジ
オルガノボ9vaキチシ組成物t−適宜のキャ響ヤー上
感ニー布、吹き付けまたは注檄するか、あるいは−ツビ
シグ1分出しシーティジグなどの手段で行えばよいか、
この賦形体はその厚みが大きすぎると、硬化触媒11た
は硬化触媒を含むオルガツボダシaキψシ組成物との界
闇播触後のその内部における架橋反応が遍くなり、その
硬化が必ずしも完全にならないので、これはその厚さが
tooo、s■以下、好ましくは5o。
ll in the production of the i/1 Kosi rubber molded article of the present invention!
The components are diorganopo9VAKinashiM compositions that do not undergo crosslinking reaction by themselves, and include diorganopo9VO group ψy group acids of heat-cured potatoes that do not contain curing catalysts such as organic peroxides, and vinyl group In the presence of a platinum thread catalyst, an addition reaction is carried out between the containing organoborisiloxane and the organohede ajesipolysiloxane containing -81H crystals in the presence of a platinum thread catalyst. Examples include those containing diplatinum thread catalysts, but these are also known as so-called two-component room-temperature curable (R'l'V) compositions, in which only the main ingredient of this two-component type is used. *'lcFor this two-component type, which mixes equal amounts of A and B, the A or B
Examples include liquids alone. These diorganopolysia acids are used as viscous bodies that flow viscously at room temperature, do not flow at room temperature, or as viscoelastic bodies that exhibit a plasticity of 5 oo or less on a William plasticity meter. However, it is preferable that this material is shaped in advance into a desired shape containing a curing catalyst that causes a crosslinking reaction or this curing catalyst. It can be done by using a suitable knee cloth, spraying or pouring, or by means such as Tubisig 1-minute sheeting jig.
If the thickness of this excipient is too large, the cross-linking reaction within the excipient after the field dissemination with the curing catalyst 11 or the curing catalyst-containing organizer screw composition will become uneven, and the curing will not necessarily be completed completely. Therefore, the thickness is less than 5 mm, preferably 5 mm.

pwa以下、さら6:好1L<t1200pm以下とす
ることがよい、しかし、この賦形は必ずしも必要″eは
なく、後記するs2成分の賦形体にこのSt成分の流動
体を注型して両者を界面播触させてもよい。
pwa or less, and preferably 6:1L<t1200pm or less. However, this shaping is not necessarily necessary, and the fluid of the St component is cast into the shape of the s2 component described later, and both are may be brought into contact with the interface.

本発明のシダフーシゴム成形品を得るための1=成分は
、@記したIII成分−二架橋反応を起させリシロキサ
ン組成物であり、これは第1成分が加熱硬化型のジメチ
ルボ9vaキ夛ンであれば有機過酸化物、それか付WB
L応型のものであればIIl成分としてのビニル基含有
ボッyaキfyと反応させるべきオルガノへイドロジエ
シボリシaキtン1したはこれC二白金、自費化合物を
添即したものとされるが、それが二液性RTV組成物で
あればこの纂l成分がその主剤のある場合の助痢1例え
ばその硬化触媒など、あるいは纂!成分として使用され
た人1wtたは1液と混合されるB液tだは人波、さら
4:はこれ1:各種の硬化触媒管配合したものとすれば
よい。そして、このlI2成分が1記した纂l成分とし
てのジオルガノボVVaキナン組成物の硬化触媒だけか
らなる場合、本発明の夷NC二当って、この硬化触媒は
その家−あるいはこれt有機溶剤で稀釈して、これをi
st成分から作られた賦形体に散布、塗布あるいは吹き
付ければよいが、この′@2成分が硬化触媒を含むオル
ガノボリシaキ夛ン組成物である場合酸二はこれt予じ
め賦形してから襲!成分と界#接触させればよい。
Component 1 for obtaining the molded Shidafushi rubber product of the present invention is a resiloxane composition which causes a two-crosslinking reaction with component III described at @, and this is a composition in which the first component is a heat-curable dimethyl carbon 9va compound. Organic peroxide if available, or WB
If it is of the L-responsive type, it is said to be an organohydrogen which is to be reacted with a vinyl group-containing compound as a component II, to which is added platinum and a proprietary compound. However, if it is a two-component RTV composition, this component can be used as a main ingredient, such as a curing catalyst, or as a component! The B liquid used as a component may be 1wt or 1wt mixed with the 1st liquid, and the B liquid t may be mixed with the 1wt or 1st liquid, and 4: This 1: Various curing catalyst tubes. When this component consists only of the curing catalyst of the diorganovo VVa quinane composition as the component described in 1, in the case of the NC of the present invention, this curing catalyst can be diluted with an organic solvent. and this is i
It may be applied by spraying, coating or spraying onto the excipient made from the st component, but if this component is an organoboric acid composition containing a curing catalyst, the acid di may be preformed. Then attack! All you have to do is bring it into contact with the component.

しDAし、この賦形は必ずしも必要でなく、この第2成
分のvK!成分との界面接触flill成分の賦形体を
含む金内感:注入したり、あるいはこの賦形体4二愉布
、ふきつけすることによって行なってもよい。な2、こ
の1B!!成分の賦形はlIl成分の賦形と同様C:適
宜のキャリヤー上−二これ全替布、ふきつけたり、ある
いはこのキャリヤー中への注Φ5二よって行なうことが
でき、これば1また他の流延加工、任縮ll!形、射出
成形で行なってもよいが、これについてはこのlI2成
分を構成するオルガツボqvaキサン組成物が完全≦二
は硬化せず、ここに含まれている硬化触媒がまだ硬化触
媒機能を残存している状態にしておく必要がある。
However, this excipient is not necessarily necessary, and the vK of this second component! Interfacial contact with components: contact with fill components containing excipients may be carried out by injection or by wiping the excipients. 2, this 1B! ! The shaping of the component can be carried out in the same manner as the shaping of the lIl component by wiping or wiping it on a suitable carrier, or by pouring it into the carrier. Rolling and shrinking! This may be done by molding or injection molding, but in this case, the organacuate qvaxane composition constituting the lI2 component is not completely cured and the curing catalyst contained therein still retains its curing catalyst function. You need to keep it in the same state.

この鳴l成分と82成分との界面接触はこの両番の賦形
体の盲ね合わせ、積層−二よって行なうが値家しく、こ
れ5二よれば第2成分中の硬化触媒の作用が容!i!l
にml成分に及ぶけれども、この賦形は第1成分、II
2成分の何れか−1としてこの賦形体1:賦形されてい
ない成分+m布、注1してもよいし、あるいはいずれも
賦形体とせず、向暑は流動状で播触させ、硬化後1:賦
形することとしてもよい。
This interfacial contact between component 82 and component 82 is achieved by blind folding and lamination of the two excipients, but according to this 52, the action of the curing catalyst in the second component is effective! i! l
ml component, but this excipient is suitable for the first component, II.
Either of the two components - 1 may be this shaped body 1: unshaped component + m cloth, Note 1, or neither of the two components may be used as a shaped body, and the heat treatment is spread in a fluid state, and after curing. 1: It may be shaped.

本発明以前配したように加熱硬化型、 1iii硬化型
のいずれにも適用することができるが、加熱硬化型のオ
ルガツボ菅Vaキ夛ン組成物を使用する場合においてこ
のml成分とlI2成分を重ね合わせあるいは積層して
からこれを加熱、または加圧加熱すると、この硬化触媒
を含まないジオルガノボ9VC1キナシ組成物のフa−
が充分−二行なわれるので、これによれば金型設計通り
の残歪のないシリフーyゴム成形体が容易に取得される
という有利性が与えられ、このシリコーシゴム累材とし
て二液性室温硬化型組成物を使用する場合S二はこの二
液を予じめ混合する必要が吻(、シたがってこの混合後
の脱気工程を省略することができるほか、仁れC:Lれ
はポットライフの間−も解決され、さら−:は成−機の
洗鹸も不要になるという優位性が与えられる。
As mentioned before the present invention, it can be applied to both the heat-curing type and the 1III-curing type, but when using a heat-curing type organacupoint Va composition, the ml component and the lI2 component are superimposed. When heated or heated under pressure after being combined or laminated, the hardening catalyst-free Diorganovo 9VC1 Kinashi composition is cured.
Since this process is carried out sufficiently twice, it is advantageous that a silicone rubber molded product with no residual strain as designed by the mold can be easily obtained. When using the composition S2, it is necessary to mix these two liquids in advance (therefore, the degassing step after mixing can be omitted, and the pot life will be reduced. This also provides the advantage of eliminating the need for washing the washing machine.

本発明は各種電子部品の製造直:広く使用することがで
き、これは例えば重電性付与剤を含有するが硬化触媒は
含んでいない流動性オルガツボダシaキナンを金型キャ
ビティの接点部分冨:注型し、ついで硬化触媒を含む絶
縁性のオルガノボリシaキナン組成物をその上直二注入
してから、これらを加熱硬化させれは重電性ゴム得点付
押釦スイッチカバー成形体を容具に、しかも接点部材の
位置づれもなく取得丁為ことができる。11た、この場
合。
The present invention can be widely used in the production of various electronic parts, for example, in the contact area of the mold cavity, using a fluidized organometallic acid quinane containing a heavy charge imparting agent but not a curing catalyst. After molding, an insulating organoboric a-quinane composition containing a curing catalyst is directly injected onto the mold, and these are heated and cured. It is possible to acquire data without shifting the position of the contact member. 11. In this case.

金型キャビティのシップ@S:着色剤としての会鵜粉末
tS入したシブフーシゴム組成物を注型しておけば、金
属光沢s感−着色されたキイ管tつ押釦スイッチカバー
成形体1得ることができ、硬化触媒を含有する絶縁性の
オルガツボ!lvaキ夛ン組酸物で上下−二貫通する細
孔1または平行間l!i[tもつ賦形体を作り、との細
孔または平行間I[J二重電性付与陶管含有するが硬化
触II&を含まないジオルガノボリシaキ葉ン組酸物管
注入し、これらt加熱硬化させれば導電都と絶msが交
互5:成形されたエラスチツクコネクターを容易に製造
する仁とができる。
Ship@S in the mold cavity: By casting the Shibufushi rubber composition containing the Aiko powder tS as a coloring agent, it is possible to obtain a colored key tube switch cover molded body 1 with metallic luster. An insulating orgapot containing a curing catalyst! 1 or parallel pores 1 or 2 penetrating from above and below in lva combination acid compound! Prepare an excipient with i[t, inject diorganoborisiac acid tubes containing porcelain tubes with double electrification but not containing hardening catalysts II&, and heat them. When cured, alternating conductive metals and solid metals are formed, which facilitates the production of molded elastic connectors.

これt−委するに、X発明6二よるシリツーy成形品は
硬化触媒を含まず、それ故にポットライフやゲル化につ
いて全く必配のないtルガノボ9t/Clキサン組成物
で一次賦形体を作り、これを硬化触媒との接触C二よっ
て硬化させるものであるし、この硬化触媒との接触はこ
の触媒管含有するオルガノボリシロキナシ組成物あるい
はその成形体との接触によって行なうこともでき、この
場合g二はその両1iを完全−二一体成形品とすること
ができるので、これ−二よれば従来品におけゐ種々の不
利を解決したシリフーシゴム成形品管容易i:、かつ効
率れゐ。
In conclusion, the molded product according to Invention X does not contain a curing catalyst, and therefore has no pot life or gelation at all. This is cured by contact C2 with a curing catalyst, and the contact with the curing catalyst can also be carried out by contacting with the organoborisiloxane composition containing the catalyst tube or a molded article thereof. In case g2, both 1i can be made into a complete two-piece molded product, so according to this case, it is possible to create a silicone rubber molded pipe that solves various disadvantages of conventional products.It is easy and efficient. .

つぎ1:本発明の実施例をあげる。Next 1: Examples of the present invention will be given.

夷に例 L 一般成形用加島硬化金透明シツフーンゴムKE6s〇−
υC信越化学工業製・部品名3100部に、その硬化触
媒C−2(信越化学工業社製・商品名)を3.5111
を添加し、ミキVングa−ルでよく混練してからカレン
ダーミールで厚さ100声鳳のフィルム状に分出した。
Example L Kashima hardened gold transparent rubber for general molding KE6s〇-
3,100 parts of υC manufactured by Shin-Etsu Chemical Co., Ltd., and 3.5111 parts of the curing catalyst C-2 (manufactured by Shin-Etsu Chemical Co., Ltd., trade name).
was added to the mixture, thoroughly kneaded in a mixing bowl, and then separated into a film with a thickness of 100 mm using a calendar meal.

つぎ1:同じく一般成1用加熱硬化染の串11性黒色v
ttフーンゴム[1131701−U (信越化学工業
社製・商品名)管tキシングロールでよく再練りし、カ
レンダーミールで厚さ100声mのフィルムとして分出
し、これと上記のフィルムを交互に多重に積層して厚さ
20G−の積層体管作り、これtrso℃で約110m
1二まで圧縮してからMail温度lsO℃1周囲温度
160Cの条件で厚さ50m!家で熱圧成形したと仁ろ
、 1lIisか完全に一体成形されたシラコーンゴム
板状体が得られた。
Next 1: Same heat-cured dyed skewer 11 black v for general production 1
tt Foon rubber [1131701-U (manufactured by Shin-Etsu Chemical Co., Ltd., trade name)] Thoroughly kneaded with a tube t kissing roll, divided into a film with a thickness of 100 mm using a calendar meal, and layered this and the above film alternately. Laminate them to make a 20G-thick laminate tube, which is about 110m at trso℃.
After compressing to 12, the thickness is 50m under the conditions of mail temperature lsO ℃ 1 ambient temperature 160C! After hot-press molding at home, a completely integrally molded silicone rubber plate was obtained.

ついで、この板状体をその積層方向J:l[角−=切断
したところ、絶−性龜と椰亀性都が!l0p11のピッ
チで積層された縞模様状のコネクターか得られ、このも
のは絶繍牲部と411牲部が完全に一体化され、その導
電性間の絶縁も完全であった。
Then, when this plate-like body was cut in the stacking direction J:l [corner-==, there was an absolute kettle and a palm cutlet! A striped connector was obtained in which layers were stacked at a pitch of 10p11, in which the embroidered part and the 411st part were completely integrated, and the insulation between the conductive parts was also perfect.

実施例1 押出し成形用加熱硬化型シリコーンゴムK1151−U
(信越化学工業社製・商品名)1:その触媒としての0
−2(II出)α8mと0−s(信越化学工業社製・商
品名)41B?添加してミキVングa−ルでよく混練り
し、カレンダーロールで厚″5tooμmのフィルムと
して分出し、ついで130℃の熱間ロールで加熱して厚
さ7 G pmのフィルムとした。
Example 1 Heat-curable silicone rubber for extrusion molding K1151-U
(manufactured by Shin-Etsu Chemical Co., Ltd., product name) 1: 0 as the catalyst
-2 (II output) α8m and 0-s (manufactured by Shin-Etsu Chemical Co., Ltd., trade name) 41B? The mixture was added and thoroughly kneaded in a mixer bowl, separated into a film with a thickness of 50 μm using a calendar roll, and then heated with a hot roll at 130° C. to form a film with a thickness of 7 G pm.

つぎ6二このフィルムに##11牲二液を液状射出成@
用シリコーンゴムlB1941 (信越化学工業社製・
部品名)のA液管厚さ50μmにドーピングし−これら
を220μm lニー81層し、160℃の黒数間で圧
縮成形して厚さ200 pmの成形体を得た。
Next, ##11 sacrificial liquid was injected onto this film in liquid form.
Silicone rubber 1B1941 (manufactured by Shin-Etsu Chemical Co., Ltd.)
A liquid tube (part name) was doped to a thickness of 50 μm, and these were layered in 81 layers of 220 μm l, and compression molded at 160° C. to obtain a molded product with a thickness of 200 pm.

なお、このブロック状成形txt!−その梼鳩方向直二
11:1111:切断したところ、ieIm層が70.
am 、aJ電11が30μmの交互積層体が得られ、
この積層体tさらにその積層万@こ1−×2−〇蛤影I
!lT面形状をもつ棒状体としたものはその積層方回直
二1.5倍の伸張をしても切断することがなかつに0実
施例3゜ 導電性の二tvntti状射出成Φ用シリコーンゴムK
R1941(前出)の人波を加熱されている押釦スイッ
チの金型キャビティの接点相当部6二滴下して厚さ0.
2−の重電牲播点i:賦形し、ついでこれに成形用加熱
硬化型の絶縁性V9コーンゴムKE951−U(ffl
越化学工業社製・商品名)100!itiにその硬化触
媒0−3(10出)3!alt−添加し、iキシングミ
−ルでよく混練しにオルガノポリシロキチン組成物を押
釦トップ部として厚さ5−に成形し、加圧即熱したとこ
ろ、これらは一体成形品として硬化され、これは押釦ス
イッチとして良好1:作動した。
In addition, this block-shaped molding txt! - The ieIm layer was 70.
An alternating laminate with am and aJ electrodes 11 of 30 μm was obtained,
This laminate t and ten thousand of its laminates
! A rod-shaped body with a T surface shape does not break even when stretched 1.5 times in the direction of its lamination. K
Two drops of R1941 (mentioned above) were applied to the contact area 6 of the heated push button switch mold cavity to a thickness of 0.
2-Heavy electrical dissemination point i: Shape, then heat-curable insulating V9 cone rubber KE951-U (ffl
Manufactured by Etsu Kagaku Kogyo Co., Ltd. (Product name) 100! The curing catalyst 0-3 (out of 10) 3! The organopolysilochitin composition was added to the top part of the push button and kneaded well in an i-xing mill, and then molded to a thickness of 5 cm as a push button top part. Good as a push button switch 1: Operated.

実施例4゜ ボッティング成形用二液性常温硬化@IVツコーンゴム
KK102RTV(信越化学社製−商品名)の硬化触媒
管含有しない液t1その表面に離型刑を塗布したポリエ
チレンテレフタレートフィルム上i二50μmの厚さi
ニキャスティングし、ついでその表面にその硬化触媒0
−RH(信越化学工業社製・商品名)を吹きつけたのち
、25℃で8Wj間放随したところ、ilu化した厚さ
50μmのり9コーンゴムフイルムが得られ、これ4二
は気泡の存在が認められなかった・ 夷ml551゜ ボッティング市二液性低ll1th#I!化金シリコー
ンゴムKKi06LTV(信越化学工業社11φ曲品名
)の硬化触媒を含有しない液を、2g!−X25@lX
3−のフェノール樹脂製容器区二深さ2m!で注入し、
ついでこの液面5二その硬化触媒でアル0−RG(信越
化学工業社製・商品名)をこの液面がさら6二1−上昇
するまで注入し、こ五を容器ごと100℃のオーブン鑑
二人れにところ、l特開に表面はゴム状を呈していたか
、容器低aは未だ充分硬化していないので、ついでこれ
?150Cのオーブンg二30分間入れてから取出した
ところ、底部はtだ粘性流動体で中間層はゲル状となっ
てい、だが、上表面0.8−は完全硬化したゴム状物と
なっていた。
Example 4 Two-component room-temperature curing for botting molding @IV Tsukone Rubber KK102RTV (manufactured by Shin-Etsu Chemical Co., Ltd. - trade name) Curing catalyst tube-free liquid t1 On a polyethylene terephthalate film whose surface was coated with a mold release agent I2 50 μm thickness i
and then apply the curing catalyst on the surface.
-RH (manufactured by Shin-Etsu Chemical Co., Ltd., trade name) was sprayed and left to stand for 8Wj at 25°C, resulting in an ilu-cone rubber film with a thickness of 50μm, which is due to the presence of air bubbles. was not recognized・夷ml551゜Botting City Two-Part Lowll1th#I! 2g of Kakin silicone rubber KKi06LTV (Shin-Etsu Chemical Co., Ltd. 11φ product name) liquid that does not contain a curing catalyst! -X25@lX
3- Phenolic resin container section 2 depth 2m! Inject with
Next, Al0-RG (manufactured by Shin-Etsu Chemical Co., Ltd., trade name) was injected into the liquid level using the curing catalyst until the liquid level rose further 621 degrees, and the container was placed in an oven at 100°C. The two of us noticed that the surface of the container had a rubber-like appearance, and that the surface of the container had not yet sufficiently hardened. When I put it in the oven at 150C for 230 minutes and took it out, I found that the bottom part was a viscous fluid and the middle layer was gel-like, but the top surface was a completely cured rubbery substance. .

実施例6゜Example 6゜

Claims (1)

【特許請求の範囲】 l)それ自体だけでは架橋反応しないジオルガノ 3゜
ポツシaキ夛ン組成物と、この組成物g二架橋反応を起
させる硬化触媒まにはこの硬化軸at含むオルガノポリ
シロキチン組成物との界面偕触(=よって両者を一体成
形品としてなるシリコーンゴム成形体。 2)それ自体だけでは架橋しないジオルガノポリシロキ
チン組成物の賦形体に、この組成物−二架橋反応を起さ
せる硬化触媒またはこの硬化触媒を含むオルガノシロキ
ナシ組成物tた以その賦形体を界面接触させ、両者を一
体成脅品とすることを特徴とするシリコーンゴム成形体
の製造方法。 3)硬化触媒を含有するオルガノポリシロキチン組成物
の賦形体の空IFjitli(:、それ自体だけでに条
横反応しないジオルガノボ9(/ロキをン組成物を注型
し、内tを一体成形品とすることを特徴とするりリコー
ンゴム成形体の製造方法。
[Scope of Claims] l) A diorganopolysiloxane composition that does not undergo a crosslinking reaction by itself, and a curing catalyst that causes the crosslinking reaction, or an organopolysilyl resin containing the curing axis at. Interfacial contact with the chitin composition (=therefore, a silicone rubber molded article in which both are integrally molded. 2) This composition-di-crosslinking reaction is applied to the excipient of the diorganopolysilochitin composition that does not crosslink by itself. 1. A method for producing a silicone rubber molded article, which comprises bringing into interfacial contact a curing catalyst that causes curing catalyst or an organosilokinashi composition containing this curing catalyst, and a molded object thereof to form an integral product. 3) Casting a diorganopolysilochitin composition containing a curing catalyst, which does not react on its own, and integrally molding the inner part. 1. A method for producing a silicone rubber molded article.
JP16462581A 1981-10-15 1981-10-15 Silicone rubber molded body and manufacture thereof Granted JPS5865643A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16462581A JPS5865643A (en) 1981-10-15 1981-10-15 Silicone rubber molded body and manufacture thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16462581A JPS5865643A (en) 1981-10-15 1981-10-15 Silicone rubber molded body and manufacture thereof

Publications (2)

Publication Number Publication Date
JPS5865643A true JPS5865643A (en) 1983-04-19
JPH028582B2 JPH028582B2 (en) 1990-02-26

Family

ID=15796747

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16462581A Granted JPS5865643A (en) 1981-10-15 1981-10-15 Silicone rubber molded body and manufacture thereof

Country Status (1)

Country Link
JP (1) JPS5865643A (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5490375A (en) * 1977-12-28 1979-07-18 Toyoda Gosei Kk Method of treating surface of rubber
JPS5515873A (en) * 1978-07-21 1980-02-04 Toyota Motor Corp Wiper blade rubber and manufacturing method

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5490375A (en) * 1977-12-28 1979-07-18 Toyoda Gosei Kk Method of treating surface of rubber
JPS5515873A (en) * 1978-07-21 1980-02-04 Toyota Motor Corp Wiper blade rubber and manufacturing method

Also Published As

Publication number Publication date
JPH028582B2 (en) 1990-02-26

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