JPS5889351A - Manufacture of independent cellular silicone rubber utilizing silk screen printing method - Google Patents
Manufacture of independent cellular silicone rubber utilizing silk screen printing methodInfo
- Publication number
- JPS5889351A JPS5889351A JP56186841A JP18684181A JPS5889351A JP S5889351 A JPS5889351 A JP S5889351A JP 56186841 A JP56186841 A JP 56186841A JP 18684181 A JP18684181 A JP 18684181A JP S5889351 A JPS5889351 A JP S5889351A
- Authority
- JP
- Japan
- Prior art keywords
- silicone rubber
- silk screen
- capsule
- screen printing
- printed
- 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.)
- Pending
Links
- 239000004945 silicone rubber Substances 0.000 title claims abstract description 58
- 229920002379 silicone rubber Polymers 0.000 title claims abstract description 54
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- 238000000034 method Methods 0.000 title abstract description 7
- 238000007650 screen-printing Methods 0.000 title abstract description 7
- 230000001413 cellular effect Effects 0.000 title abstract 2
- 239000002775 capsule Substances 0.000 claims abstract description 14
- 239000000203 mixture Substances 0.000 claims abstract description 13
- 239000004088 foaming agent Substances 0.000 claims abstract description 8
- 238000009835 boiling Methods 0.000 claims abstract description 5
- 229920001577 copolymer Polymers 0.000 claims abstract description 5
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 5
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 5
- 229920001971 elastomer Polymers 0.000 claims description 7
- 238000005187 foaming Methods 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 5
- 239000000806 elastomer Substances 0.000 claims description 3
- 239000002245 particle Substances 0.000 claims description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 2
- 239000004215 Carbon black (E152) Substances 0.000 abstract description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- -1 methyl phenyl vinyl Chemical group 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- 238000009833 condensation Methods 0.000 description 5
- 230000005494 condensation Effects 0.000 description 5
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 239000006260 foam Substances 0.000 description 5
- 229920002631 room-temperature vulcanizate silicone Polymers 0.000 description 5
- 239000004604 Blowing Agent Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 229920001296 polysiloxane Polymers 0.000 description 4
- 238000007639 printing Methods 0.000 description 4
- 239000005060 rubber Substances 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000003431 cross linking reagent Substances 0.000 description 3
- 239000013013 elastic material Substances 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 150000002978 peroxides Chemical class 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229920005645 diorganopolysiloxane polymer Polymers 0.000 description 2
- HIHIPCDUFKZOSL-UHFFFAOYSA-N ethenyl(methyl)silicon Chemical compound C[Si]C=C HIHIPCDUFKZOSL-UHFFFAOYSA-N 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 150000001451 organic peroxides Chemical class 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 238000004073 vulcanization Methods 0.000 description 2
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 102100032392 Circadian-associated transcriptional repressor Human genes 0.000 description 1
- 101710130150 Circadian-associated transcriptional repressor Proteins 0.000 description 1
- VTDQEFPUJUZPCC-UHFFFAOYSA-N N-butan-2-ylidenehydroxylamine silane Chemical compound [SiH4].CCC(C)=NO VTDQEFPUJUZPCC-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 235000016496 Panda oleosa Nutrition 0.000 description 1
- 240000000220 Panda oleosa Species 0.000 description 1
- 229910000805 Pig iron Inorganic materials 0.000 description 1
- 241000282806 Rhinoceros Species 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- IDCBOTIENDVCBQ-UHFFFAOYSA-N TEPP Chemical compound CCOP(=O)(OCC)OP(=O)(OCC)OCC IDCBOTIENDVCBQ-UHFFFAOYSA-N 0.000 description 1
- MRZRNRPDICXPOU-UHFFFAOYSA-N [SiH4].CC(C)=NO Chemical compound [SiH4].CC(C)=NO MRZRNRPDICXPOU-UHFFFAOYSA-N 0.000 description 1
- KXJLGCBCRCSXQF-UHFFFAOYSA-N [diacetyloxy(ethyl)silyl] acetate Chemical compound CC(=O)O[Si](CC)(OC(C)=O)OC(C)=O KXJLGCBCRCSXQF-UHFFFAOYSA-N 0.000 description 1
- TVJPBVNWVPUZBM-UHFFFAOYSA-N [diacetyloxy(methyl)silyl] acetate Chemical compound CC(=O)O[Si](C)(OC(C)=O)OC(C)=O TVJPBVNWVPUZBM-UHFFFAOYSA-N 0.000 description 1
- 238000012644 addition polymerization Methods 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- CHIHQLCVLOXUJW-UHFFFAOYSA-N benzoic anhydride Chemical compound C=1C=CC=CC=1C(=O)OC(=O)C1=CC=CC=C1 CHIHQLCVLOXUJW-UHFFFAOYSA-N 0.000 description 1
- PJSDPKGKXZOTCP-UHFFFAOYSA-N butane pentane Chemical compound CCCC.CCCCC.CCCCC PJSDPKGKXZOTCP-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000006356 dehydrogenation reaction Methods 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 125000005816 fluoropropyl group Chemical group [H]C([H])(F)C([H])([H])C([H])([H])* 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 150000002505 iron Chemical class 0.000 description 1
- UCSUOYMTZRJAIH-UHFFFAOYSA-N iron(2+) oxygen(2-) titanium(4+) Chemical compound [O-2].[O-2].[Ti+4].[Fe+2] UCSUOYMTZRJAIH-UHFFFAOYSA-N 0.000 description 1
- KEHCHOCBAJSEKS-UHFFFAOYSA-N iron(2+);oxygen(2-);titanium(4+) Chemical compound [O-2].[O-2].[O-2].[Ti+4].[Fe+2] KEHCHOCBAJSEKS-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LAQFLZHBVPULPL-UHFFFAOYSA-N methyl(phenyl)silicon Chemical compound C[Si]C1=CC=CC=C1 LAQFLZHBVPULPL-UHFFFAOYSA-N 0.000 description 1
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 150000004714 phosphonium salts Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 125000005372 silanol group Chemical class 0.000 description 1
- 150000004819 silanols Chemical class 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/14—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
- C08J9/141—Hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2383/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon only; Derivatives of such polymers
- C08J2383/04—Polysiloxanes
Abstract
Description
【発明の詳細な説明】
本発明はシルクスクリーン印刷法を利用して独立気泡性
のシリコーンゴム弾性体を製造する。方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention uses a silk screen printing method to produce a closed-cell silicone rubber elastomer. Regarding the method.
一般にシリコーンゴム弾性体は他のゴム弾性体に比較し
て、耐熱性、耐薬品性、耐候性などに優れているため、
バッキング、ガスケットなどにも広く利用されている。In general, silicone rubber elastic bodies have superior heat resistance, chemical resistance, weather resistance, etc. compared to other rubber elastic bodies.
It is also widely used for backings, gaskets, etc.
しかしながら、シリコーンゴム弾性体でノ臂ツキングや
ガスケットを製造する場合、従来は所定の厚さを有する
シート状シリコーンゴム弾性体を用意し、このシートを
所望の形状に打抜く方法が採用されているため、シート
にかなシの無駄が出る欠点があった。However, when manufacturing armrests or gaskets using silicone rubber elastic material, the conventional method has been to prepare a sheet-like silicone rubber elastic material with a predetermined thickness and punch this sheet into the desired shape. Therefore, there was a drawback that there was a waste of kana on the sheet.
本発明者は未加硫もしくは未硬化のシリコーンゴムがシ
ルクスクリーン印刷に使用可能な粘at有していること
に着目し、シルクスクリーン印刷法で所望の形状に印刷
されたシリコーンゴムは。The present inventors have focused on the fact that unvulcanized or uncured silicone rubber has a tack that can be used for silk screen printing, and the silicone rubber that has been printed into a desired shape using the silk screen printing method.
これを単に加硫もしくは硬化させただけでは、ノ々ツキ
ング乃至ガスケットとしての厚さが不足するけれども、
これt連続気泡ではなく独立気泡構造に発泡させれば、
バッキング乃至ガスケットとして必要な厚さが得られる
ので、シリコーンゴムを徒費することなく、79ツキン
グ乃至ガスケットに使用可能な独立気泡性シリコーンゴ
ム弾性体が得られることを見い出した。If this is simply vulcanized or hardened, it will not be thick enough to be used as a notching or gasket.
If the foam is made to have a closed cell structure instead of an open cell structure,
It has been found that a closed-cell silicone rubber elastic body that can be used for backings or gaskets can be obtained without wasting silicone rubber because the thickness required for backings or gaskets can be obtained.
而して本発明の方法は加熱加硫型シリコーンゴム又は常
温加硫型シリコーンゴムに1粒径が10〜30μmの範
Hにあり、塩化ビニリゾy共重合物で形成された皮殻内
に低沸点炭化水素を内包させたカプセル発泡剤を、シリ
コーンゴム100重量部当り1.0〜20重量部の割合
で混合し、この混合物にて支持体上に所望の形状をシル
クスクIJ−ン印刷の手法で印刷し9次いで支持体上に
印刷されたものを50〜150℃の温度範囲で1〜20
分間熱処理して発泡させることからなる。Therefore, the method of the present invention has a heat-vulcanized silicone rubber or a room-temperature vulcanizable silicone rubber with a grain size in the range H of 10 to 30 μm, and a low-temperature vulcanized silicone rubber in a shell formed of a vinyl chloride y copolymer. A capsule blowing agent containing a boiling point hydrocarbon is mixed at a ratio of 1.0 to 20 parts by weight per 100 parts by weight of silicone rubber, and a desired shape is printed on a support using this mixture using a silk screen IJ-printing method. 9 Then, the printed material on the support was heated at a temperature range of 50 to 150°C for 1 to 20°C.
It consists of a heat treatment for a minute and foaming.
本発明に於て、シリコーンゴムとしては加熱加硫型と常
温加硫型のいずれもが使用可能である。In the present invention, both heat vulcanization type and room temperature vulcanization type silicone rubber can be used.
加熱加硫型のシリコーンゴムには、ジメチルシリコーン
ゴム、メチルフェニルシリコーンゴム、メチルビニルシ
リコーンゴム、メチルフェニルビニルシリコーンゴム、
メチルフルオルゾロビルシリコーンゴムナトがある。ジ
メチルシリコーンゴムは最4/fニラ−であるが、メチ
ル基の一部をビニル基で置き換えたメチルビニルシリコ
ーンゴムけ、常圧熱気加硫が可能であシ、圧縮永久歪な
どの物性の点でジメチルシリコーンゴムより優れている
。またフェニル基を有するシリコーンゴムは低温特性に
優れ、フルオルプロピル基含有するシリコーンゴムは耐
溶剤性が良好である。従って。Heat-curable silicone rubbers include dimethyl silicone rubber, methylphenyl silicone rubber, methyl vinyl silicone rubber, methyl phenyl vinyl silicone rubber,
There is methylfluorozolobyl silicone rubber. Dimethyl silicone rubber is a 4/f dimethyl silicone rubber, but methyl vinyl silicone rubber has some of the methyl groups replaced with vinyl groups, can be vulcanized in hot air at normal pressure, and has poor physical properties such as compression set. superior to dimethyl silicone rubber. Furthermore, silicone rubber containing phenyl groups has excellent low-temperature properties, and silicone rubber containing fluoropropyl groups has good solvent resistance. Therefore.
最終的に得られる独立気泡性ゴム弾性体の使用目的に応
じて、原料に用いるシリコーンゴムの種類を選択するこ
とが好ましい。It is preferable to select the type of silicone rubber used as a raw material depending on the purpose of use of the closed-cell rubber elastic body finally obtained.
加熱加硫型シリコーンゴムは有機過酸化物、脂肪酸アゾ
化合物、硫黄、放射線などによシ加硫できるが、最も一
般的な加硫剤は有機過酸化物であって、その具体例とし
ては過酸化ベンゾイル、過酸化♂スー2’、4−ジクロ
〃ベンゾイル、過酸化ジクミル、過酸化ジターシャリ−
ブチルなどを例1示することかできる。これら加硫剤、
のシリコーンゴムに対する配合量Fil〜lO重量−の
範囲で調整することを可とする。Heat-curable silicone rubber can be vulcanized using organic peroxides, fatty acid azo compounds, sulfur, radiation, etc. The most common vulcanizing agents are organic peroxides, and specific examples include Benzoyl oxide, male peroxide 2', 4-dichlorobenzoyl, dicumyl peroxide, ditertiary peroxide
Butyl and the like can be given as an example. These vulcanizing agents,
It is possible to adjust the blending amount to the silicone rubber within the range of Fil to lO weight.
常温加硫型(RTV )シリコーンゴムとしてはl液型
と2液型のいずれもが使用可能である。l液型RTVシ
リコーンゴムは末端に水酸基を有するジオルガノポリシ
ロキサンと架橋剤とからなり。As the room temperature vulcanizable (RTV) silicone rubber, both one-component type and two-component type can be used. One-liquid type RTV silicone rubber consists of diorganopolysiloxane having a hydroxyl group at the end and a crosslinking agent.
主として空気中の水分によって縮合反応により硬化する
ものであって、この場合の架橋剤としてはメチルトリア
セトキシシラy、エチルトリアセトキシシラン(以上脱
酢酸縮合タイプ)、アセトンオキシムシラン、ブタノン
オキシムシラン(以上脱オキシム縮合タイプ〕、メチル
トリメトキシシラン、ビニルトリメトキシシラ/(以上
脱アルコール縮合タイプ)、シラザン(脱酢酸縮合タイ
プ)などが知られている。一方、2液型RTVシリコー
ンゴムは末端に官能基を持ったジオルガノポリシロキサ
ンと、架橋剤と、硬化触媒の3成分を二つに分けて2液
としたものであって、硬化機構の上から2液型RTVシ
リコーンゴムは、2種類に分類することができる。その
一つは金属有機酸塩、有機アミン、第四級アンモニウム
あるいはホスホニウム化合物などt−硬化触媒として、
シラノールとアルコキシシロキサン(、アルキルオルソ
シリケート)との脱アルコール縮合、シラノール同志の
脱水縮合、シリリジル(−1!IIH)とシラノ−ルと
の脱水素縮合によって硬化するタイプであり、他の1つ
はノぐラジウム、白金、過酸化物などを硬化触媒として
、ビニル基などと一8iHとの付加重合によって硬化す
るタイプであって、この−のけ60〜150℃に加熱す
ると急速に果橋反応が進行して硬化し、その架橋温度が
後述するカプセル発泡剤の発泡温度と合致するので、好
ましい2液型RTVシリコーンゴムである。It is mainly cured by a condensation reaction with moisture in the air, and the crosslinking agents in this case include methyltriacetoxysilane, ethyltriacetoxysilane (acetic acid removal condensation type), acetone oxime silane, butanone oxime silane (above). Oxime decondensation type], methyltrimethoxysilane, vinyltrimethoxysilane (dealcoholization condensation type), silazane (acetic acid decondensation type), etc.On the other hand, two-component RTV silicone rubber has functional terminals. The three components of diorganopolysiloxane having a group, a crosslinking agent, and a curing catalyst are divided into two parts, and two-part RTV silicone rubber is divided into two types based on the curing mechanism. One of them is metal organic acid salts, organic amines, quaternary ammonium or phosphonium compounds as t-curing catalysts.
This type is cured by dealcoholization condensation between silanol and alkoxysiloxane (alkyl orthosilicate), dehydration condensation between silanols, and dehydrogenation condensation between silylidyl (-1! IIH) and silanol. This type cures by addition polymerization of vinyl groups and 18iH using a curing catalyst such as nogradium, platinum, or peroxide, and when this mixture is heated to 60 to 150°C, the fruit bridge reaction occurs rapidly. It is a preferred two-component type RTV silicone rubber because it cures as it progresses and its crosslinking temperature matches the foaming temperature of the capsule foaming agent described later.
本発明で使用されるカプセル発泡剤は、塩化ビ二リゾ/
共重合物で形成された皮殻内に、ブタンペンタンなどの
低沸点炭化水素を内包させたものであって、その粒径は
10〜30μmの範囲にあることを可とする。この種の
カプセル発泡剤は上述したシリコーンゴムと均一に混合
!きるばかりでなく、300メツシュ以上のシルクスク
リーンを通過することができ、しかも発泡に際して皮殻
が破れることがないので独立気泡を形成することができ
る。本発明で使用可能なカプセル発泡剤の一具体例は商
品多電クロ、e−ルF−30(松本油脂製薬株式会社製
)で市販されているマイクロカプセルであって、このも
のの物性は粒径10〜30μm。The capsule blowing agent used in the present invention is vinylisochloride/
A low-boiling hydrocarbon such as butanepentane is encapsulated in a shell formed of a copolymer, and the particle size can be in the range of 10 to 30 μm. This type of capsule foaming agent mixes uniformly with the silicone rubber mentioned above! Not only can it pass through a silk screen with a mesh size of 300 or more, it can also form closed cells because the shell does not break during foaming. A specific example of a capsule foaming agent that can be used in the present invention is a microcapsule commercially available as Taden Kuro, e-le F-30 (manufactured by Matsumoto Yushi Seiyaku Co., Ltd.), and the physical properties of this product include particle size. 10-30 μm.
比重1.13g/Cfn”、軟化源[80−85℃、最
高発泡倍率70倍である。The specific gravity is 1.13 g/Cfn'', the softening source is 80-85°C, and the maximum expansion ratio is 70 times.
本発明によれば、カプセル発泡剤社シリコーンゴム10
0重量部轟り1.O〜20重量部混合する。According to the present invention, Capsule Foaming Agent Silicone Rubber 10
0 parts by weight Roaring 1. Mix 0 to 20 parts by weight.
20重量部以上混合すると、最終的に−られるシリ;−
ンゴム弾性体の物性が損われるからである。When 20 parts by weight or more are mixed, the final silicate;
This is because the physical properties of the rubber elastic body are impaired.
カプセル発泡剤とシリコーンゴムとの混合物は。Mixture of capsule blowing agent and silicone rubber.
シルクスクリーン印刷のインク相当物として取扱われ、
これを用いて任意の支持体上に所望の形状がシルクスク
リーン印刷される。印刷に用いるシルクスクリーンの目
開きは印刷パター/の精[を確保するうえで48〜30
0メツシュ程ft−可とする。支持体上の印刷パターン
は次いで50〜150℃の温度範Hで1〜20分間程度
熱処理されるが。Treated as an ink equivalent for silk screen printing,
This is used to silk screen print a desired shape onto any support. The mesh size of the silk screen used for printing is 48 to 30 to ensure the precision of the printing pattern.
ft- is allowed for about 0 meshes. The printed pattern on the support is then heat treated at a temperature range H of 50 to 150 DEG C. for about 1 to 20 minutes.
これによってカプセル発泡剤は、独立気泡構造に発泡し
、シリコーンゴム祉硬化するので、!!II立気泡性の
シリコーンゴム弾性体を得ることができる。This allows the capsule foaming agent to foam into a closed cell structure and harden the silicone rubber! ! II. A foamable silicone rubber elastomer can be obtained.
本発明では必要に応じて充填薊、fla料、その他の添
加剤を併用することができる。この種の充填剤には補強
を目的として使用されるフエームドシリカなど0シリカ
微粉末と、増量を主目的として使用されるけいそう±0
石英粉、炭酸カルシウム。In the present invention, filler material, flaring material, and other additives may be used in combination as necessary. This type of filler includes fine silica powder such as foamed silica, which is used for reinforcement purposes, and ±0 silica powder, which is used primarily to increase the volume.
Quartz powder, calcium carbonate.
クレー、アルミナ2.酸化鉄−1酸化チタン、カーーン
ブラックなど−かめる。これらのうち、Ill銑鉄酸化
チタン、カーゼンブラックなどは顔料としても使用され
る。添加剤には1例えばフエームドシリカを充填剤とし
て使用する場合、その分散促進剤として使用されるシリ
コーンレジン、アルコキシン2ン及びシロキサン、ヒド
ロキシシラン及びシロキサンなどがあり、低粘度化、低
モジユラス化などの目的ではジメチルシリコーンオイル
が好んで使用される。Clay, alumina 2. Iron oxide - titanium oxide, carn black, etc. Among these, Ill pig iron titanium oxide, casen black, etc. are also used as pigments. Additives include silicone resins, alkoxine diamines, siloxanes, hydroxysilanes, and siloxanes, which are used as dispersion promoters when made silica is used as a filler. Dimethyl silicone oil is preferably used for this purpose.
実施例1
トーレシリコーン(株]製の5H−433(加熱加硫型
シリコーンゴム)100gに、前述したミクロ/9−ル
F−30(カプセル発泡剤)sgt−加えてよく混合し
た後、加硫剤として過酸化ジターシャリ−ブチル10g
f:混合し、この均一混合物と60メツシユシルクスク
リーンを用いて添付図面に示す知歯平面形状(11””
” 2.5 mm 、 r@−wi、o ff1m 。Example 1 To 100 g of 5H-433 (heat-curable silicone rubber) manufactured by Toray Silicone Co., Ltd., the aforementioned Micro/9-L F-30 (capsule blowing agent) sgt- was added, mixed well, and then vulcanized. 10g ditert-butyl peroxide as agent
f: Mix and use this uniform mixture and a 60-mesh silk screen to form the tooth plane shape (11") shown in the attached drawing.
” 2.5 mm, r@-wi, off1m.
鴫■29mm、R,謬1511重)のノ臂ターンを厚さ
0.5mmで離型紙上に印刷した。次いで離型紙上の/
臂ターンt130℃のオーブンに15分間熱処理して発
泡させたところ、厚さがg、5ff1mに平均した独立
気泡性シリコーンゴム弾性体が得られた。A 0.5 mm thick turn was printed on release paper. Then / on the release paper
When foaming was performed by heat treatment in an oven at 130° C. for 15 minutes, a closed-cell silicone rubber elastic body having an average thickness of g and 5 ff 1 m was obtained.
発泡後の印刷パターンには寸法上のくるいはなく。There is no dimensional distortion in the printed pattern after foaming.
厚さ方向にのみ高弾性を示した。It showed high elasticity only in the thickness direction.
実施例2
トーレシリコーン(株)製の8H−780(1液型RT
Vシリコーンゴム)100gに2.5gのミクロパール
F−301によく混合し、この混合物と80メツシユシ
ルクスクリーンを用いて、水分vr:含まない窒素ガス
雰囲気中にて、半径30mm。Example 2 8H-780 (1-component RT) manufactured by Toray Silicone Co., Ltd.
V silicone rubber) was mixed well with 2.5 g of Micropearl F-301, and using this mixture and an 80 mesh silk screen, the radius was 30 mm in a nitrogen gas atmosphere containing no moisture vr.
厚さQ、ltnmの円形、41ターンtアルミ箔上に印
刷した。次いでアルミ箔上の/臂ターンt140℃のオ
ーブンにて1分間熱処理して発泡させ、しかる後温度り
5℃、湿度f3 Q % RHの室内に放置したところ
0発泡層の崩れが全くない状態で45分間後に指触硬化
し、4時間後には完全硬化して厚さQ、3mmの独立気
泡性シリ;−ンゴム弾性体を得友。It was printed on a circular, 41 turn T aluminum foil with a thickness of Q, lt nm. Next, heat treatment was performed on the aluminum foil in an oven at 140°C for 1 minute to foam, and then the foam layer was left in a room at a temperature of 5°C and a humidity of f3Q%RH, and there was no collapse of the foam layer. It hardened to the touch after 45 minutes, and completely hardened after 4 hours, yielding a closed-cell silicone rubber elastic body with a thickness of 3 mm.
このゴム弾性体は独立気泡構造を有しているため、高圧
縮弾性率を儂え、しかも液モレ1.ガスモレを全く伴わ
ないのでシートバッキングとして好適である。Since this rubber elastic body has a closed cell structure, it has a high compressive elastic modulus and also has 1.0% liquid leakage. It is suitable as a seat backing because it does not cause any gas leakage.
実施例3
トーレシリコーン(株)製の8 E −1yoo(2液
型LTVシリコーンゴム)100gに5gのミクロパー
ルF−30をよく混合し、この混合物と200メツシユ
のシルクスクリーンを用いて厚さ0.3mmの鉄板の上
に半1150mm、暢15attn。Example 3 100 g of 8E-1yoo (two-component LTV silicone rubber) manufactured by Toray Silicone Co., Ltd. was thoroughly mixed with 5 g of Micropearl F-30, and this mixture was coated with a 200-mesh silk screen to a thickness of 0. Half 1150mm, length 15attn on a .3mm iron plate.
犀さQJm+nのリング状パターンを印刷し九のち。Printed a ring-shaped pattern of rhinoceros QJm+n nine days later.
140℃にて10分間熱処理して厚さ0.6mmの独立
気泡性シリコーンゴム弾性体を得た。A closed-cell silicone rubber elastic body having a thickness of 0.6 mm was obtained by heat treatment at 140° C. for 10 minutes.
このリング状シリコーンゴム弾性体が付着した鉄板をシ
リコーンゴム弾性体が内側になるように加圧成型し、ガ
ラス容器のキャップとして使用したところ、このものは
ガ^そし、液モレを完全に防止するシール効果を発揮し
九。When this iron plate with the ring-shaped silicone rubber elastic body attached was pressure-molded so that the silicone rubber elastic body was on the inside and used as a cap for a glass container, this thing did not get wet and completely prevented liquid from leaking. 9. Demonstrates sealing effect.
実施例4
トーレシリコーン(株)製の8H−9583(2液WR
TVシリコーンゴム) loogに4gのζクロノ々−
ルF −30t−よく混合し、この混合物と60メツシ
ユのシルクスクリーンを用いて径0.!Imm、fツチ
間wk2mm 、厚み9.2mmの小点をテトロン織布
上全面に印刷し、しかる後これt−100℃で10分間
熱処理発泡させたところ、厚さが0.5〜Q、15mm
の独立気泡性シリコーンゴム弾性体を点状に有する布が
得られ良。このものは摩擦係数が大きく、またパークレ
ン−トリクレンに耐え。Example 4 8H-9583 (2-liquid WR) manufactured by Toray Silicone Co., Ltd.
TV silicone rubber) 4g of ζ chrono on loog
Mix well and use this mixture with a 60-mesh silk screen to measure the diameter of 0. ! Small dots with a width of 2 mm between Imm and f and a thickness of 9.2 mm were printed on the entire surface of Tetron woven fabric, and then heat treated and foamed at t-100°C for 10 minutes, resulting in a thickness of 0.5 to Q, 15 mm.
A cloth having dots of closed-cell silicone rubber elastic material was obtained. This material has a large coefficient of friction and can withstand per-clean and tri-clean.
耐アイロン性にも優れているので、滑シ防止用としてベ
ルト、ズiンの腰部、ショルダーノ署ッグ岬への利用が
期待できる。It also has excellent iron resistance, so it can be used to prevent slippage on belts, the waist of jeans, and shoulder straps.
添付図面は冥施例1のシルクスクリーン印刷で得九印刷
パターンの平面図である。The attached drawing is a plan view of the nine printing patterns obtained by silk screen printing of Example 1.
Claims (1)
コーンゴムに0粒径が10〜30μmの範囲にあり、塩
化ビニリゾy共重合物で形成され九皮殻内に低沸点炭化
水素を内包させたカプセル発泡剤を、シリコーンゴム1
00重量部当91.0〜′20重を部混合し、この混合
物にて支持体上に所望の形状をシルクスクリーン印刷し
、yいて支持体上に印刷されたものを50〜150℃の
温度範囲で1〜20分間熱処理して発泡させることから
なる独立気泡性シリコーンゴム弾性体の製造法。1. Heat-vulcanized silicone rubber or room-temperature vulcanized silicone rubber has a zero particle size in the range of 10 to 30 μm, is made of vinyl chloride y copolymer, and has low-boiling hydrocarbons encapsulated in its shell. Add the capsule foaming agent to the silicone rubber 1
A desired shape is silk screen printed on a support using this mixture, and the printed material is heated at a temperature of 50 to 150°C. A method for producing a closed-cell silicone rubber elastomer, which comprises foaming by heat treatment within a range of 1 to 20 minutes.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56186841A JPS5889351A (en) | 1981-11-24 | 1981-11-24 | Manufacture of independent cellular silicone rubber utilizing silk screen printing method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56186841A JPS5889351A (en) | 1981-11-24 | 1981-11-24 | Manufacture of independent cellular silicone rubber utilizing silk screen printing method |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5889351A true JPS5889351A (en) | 1983-05-27 |
Family
ID=16195564
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56186841A Pending JPS5889351A (en) | 1981-11-24 | 1981-11-24 | Manufacture of independent cellular silicone rubber utilizing silk screen printing method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5889351A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0274819A2 (en) * | 1986-12-17 | 1988-07-20 | Dow Corning Corporation | Use of a intumescent foamable composition as a flame and smoke barrier |
-
1981
- 1981-11-24 JP JP56186841A patent/JPS5889351A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0274819A2 (en) * | 1986-12-17 | 1988-07-20 | Dow Corning Corporation | Use of a intumescent foamable composition as a flame and smoke barrier |
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