CN106753201A - A kind of automotive electronics label silicon rubber bonder and preparation method thereof - Google Patents

A kind of automotive electronics label silicon rubber bonder and preparation method thereof Download PDF

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CN106753201A
CN106753201A CN201611153030.1A CN201611153030A CN106753201A CN 106753201 A CN106753201 A CN 106753201A CN 201611153030 A CN201611153030 A CN 201611153030A CN 106753201 A CN106753201 A CN 106753201A
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silicon rubber
automotive electronics
electronics label
parts
catalyst
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CN106753201B (en
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王强
毛云忠
陈世容
谢志坚
刘彬
暴玉强
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China Bluestar Chengrand Research Institute of Chemical Industry Co Ltd
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China Bluestar Chengrand Research Institute of Chemical Industry Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J183/00Adhesives based on 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; Adhesives based on derivatives of such polymers
    • C09J183/04Polysiloxanes
    • C09J183/06Polysiloxanes containing silicon bound to oxygen-containing groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K13/00Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
    • C08K13/06Pretreated ingredients and ingredients covered by the main groups C08K3/00 - C08K7/00
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/34Silicon-containing compounds
    • C08K3/36Silica
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/10Esters; Ether-esters
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/54Silicon-containing compounds
    • C08K5/541Silicon-containing compounds containing oxygen
    • C08K5/5415Silicon-containing compounds containing oxygen containing at least one Si—O bond
    • C08K5/5419Silicon-containing compounds containing oxygen containing at least one Si—O bond containing at least one Si—C bond
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/54Silicon-containing compounds
    • C08K5/541Silicon-containing compounds containing oxygen
    • C08K5/5425Silicon-containing compounds containing oxygen containing at least one C=C bond
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K9/00Use of pretreated ingredients
    • C08K9/04Ingredients treated with organic substances
    • C08K9/06Ingredients treated with organic substances with silicon-containing compounds
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    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02Non-macromolecular additives
    • C09J11/04Non-macromolecular additives inorganic
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    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02Non-macromolecular additives
    • C09J11/06Non-macromolecular additives organic
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/002Physical properties
    • C08K2201/006Additives being defined by their surface area
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
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    • C08L2201/08Stabilised against heat, light or radiation or oxydation
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    • C08L2201/10Transparent films; Clear coatings; Transparent materials

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Abstract

The invention provides a kind of automotive electronics label silicon rubber bonder and preparation method thereof, belong to silicone rubber applications technical field.The raw material of silicon rubber bonder includes sizing and auxiliary material, and addition weight of the auxiliary material with 100 parts of sizings as weight basis is:1~8 part of crosslinking agent, 0.01~0.5 part of catalyst, 0.1~2 part of co-catalyst, 0.5~5 part of tackifier, 0.1~2 part of deep layer adhesion promoters, wherein sizing include 70~88 parts of hydroxyl-terminated injecting two methyl siloxane, 12~30 parts of the reinforced filling counted by weight.Binding agent of the present invention is a kind of single-component room-temperature-vulsilicone silicone rubber of de- acetic acid type, for bonding automotive electronics label, good performance requirement, easy to operate and with rapid link effect can be not only reached, 1 hour adhesive strength is 3~4 times of the usual silicone rubber under the conditions of.

Description

A kind of automotive electronics label silicon rubber bonder and preparation method thereof
Technical field
The present invention relates to a kind of silicon rubber binding agent, in particular it relates to a kind of automotive electronics label is de- Acetic acid type silicon rubber bonder and preparation method thereof, belongs to silicone rubber applications technical field.
Background technology
Silicon rubber possesses excellent high and low temperature resistance, can be in addition also equipped with good in -60 DEG C to 200 DEG C long-term uses UV resistance, radiation-resistant property, oxytolerant ageing properties, chemical stability and electrical insulation properties, obtained in various fields To extensive use.Silicon rubber can be divided into one pack system and two-component room-temperature-vulcanized silicone rubber by its manner of packing, by vulcanization mechanism again Condensed type and add-on type can be divided into.One-component condensed type silicon rubber can be divided into again by different vulcanizing groups dealcoholized type, de-oxime type, De- acetic acid type, deacetone, de amide type etc.;Wherein, taking off acetic acid type room temperature vulcanized silicone rubber has that curingprocess rate is fast, transparency Various base materials, especially glass, ceramics, high temperature gum base materials are had excellent adhesive property by the advantages of high and low poison ring is protected.But it is single Component room temperature vulcanization silicon rubber is vulcanized by the moisture in ingress of air, when two base materials to be bonded are airtight and viscous When junction product is larger, moisture smoothly cannot enter inside adhesive linkage, the problem for causing to vulcanize inside adhesive linkage, it is impossible to reach Good adhesive effect and adhesive strength.
Vehicle electron identifying(electronic registration identification of the motor Vehicle, abbreviation ERI)Also automobile electronic identity card, Digital Automobile multi-standard source are, " electronic license plate " are commonly called as, by license plate number The information Stores such as code in RF tag, can automatically, noncontact, not parking the identification and monitoring for completing vehicle.Automobile electricity Sub-mark is formulated and promoted by state ministry of public security, is sought unity of standard by Public Security Department of the Ministry of Public Security, unified to carry out, unified pipe Reason.At present, the Ministry of Public Security is actively pushing forward vehicle electron identifying related work with Ministry of Industry and Information, it is contemplated that complete within 2014 whole newly organized Research and development and national standard authorized strength work, carry out Demonstration Application, improved and complete application in 2016 and policy safeguard in 2015.At present, The base material that vehicle electron identifying is used is ceramic substrate(100mm*60mm), installation site is automobile windscreen inner.Such as What is pasted in vehicle electron identifying problem, presently, there are two kinds of Binding schemes:Two-sided glue sticking and silicon rubber are bonded.Scheme one is Pasted using strong double-face glue.The advantage of the program is strong easy to operate, initial bonding strength;Have the disadvantage double faced adhesive tape high temperature resistant, resistance to The poor performances such as water, UV resistance, under suitable conditions(Such as it is heated to 100 DEG C), electronic mark completely can be removed easily. Scheme two is bonded electronic mark using silicon rubber, and its resistance to environmental aging performance will be substantially better than scheme one, but it has the disadvantage single group Part room temperature vulcanized silicone rubber is progressively solidified by steam in ingress of air, and the short time cannot deep layer vulcanization, potsherd middle part silicon rubber Glue vulcanization is incomplete, largely reduces the adhesive effect of silicon rubber.Especially at the bonding initial stage(In 2 hours), it is only ceramic The silicon rubber vulcanization of substrate edge, after such as destroying adhesive linkage edge using cutter, fret saw instrument, can be by electronic mark It is complete to remove.Based on this, develop the high intensity that a kind of automotive electronics label is equipped with, can rapid deep zone bonding, with good The de- acetic acid type room temperature vulcanized silicone rubber of the one-component of good tamper effect is very necessary.
The content of the invention
It is a first objective of the present invention to provide a kind of automotive electronics label silicon rubber bonder.The binding agent is one The single-component room-temperature-vulsilicone silicone rubber of de- acetic acid type is planted, for bonding automotive electronics label, can not only reach good performance will Ask, it is easy to operate and with rapid link effect, 1 hour adhesive strength is 3~4 times of the usual silicone rubber under the conditions of.
Another object of the present invention is to, there is provided a kind of preparation method of automotive electronics label silicon rubber bonder.
For achieving the above object, the technology used in the present invention method is as follows:
A kind of automotive electronics label silicon rubber bonder, it is characterised in that:Raw material includes sizing and auxiliary material, the auxiliary material With 100 parts of sizings as the addition weight of weight basis is:
1~8 part of crosslinking agent
0.01~0.5 part of catalyst
0.1~2 part of co-catalyst
0.5~5 part of tackifier
0.1~2 part of deep layer adhesion promoters
The sizing includes 70~88 parts of hydroxyl-terminated injecting two methyl siloxane, the reinforced filling 12~30 counted by weight Part.
Wherein, the hydroxyl-terminated injecting two methyl siloxane is 107 glue, is the poly- of 3000~20000mPaS selected from viscosity One kind or any several mixture in siloxanes.It is preferred that 107 glue of 5000~10000mPaS viscosity.
The reinforced filling is hydrophilic or hydrophobic type fume colloidal silica.Wherein preferred hydrophobic type fume colloidal silica, Most preferably 100~the 300m of specific surface area of silazane treatment2The hydrophobic type fume colloidal silica of/g.
The crosslinking agent be methyl triacetoxysilane, ethyltriacetoxysilane, propyl group triacetoxysilane, At least one in vinyltriacetoxy silane.
The catalyst is at least in dibutyl tin dilaurate, dibutyl tin dioctoate, dibutyl tin acetate Kind.
The co-catalyst is containing zinc(Zn), titanium(Ti)Or molybdenum(Mo)Deng the compound of element;Further, as metatitanic acid four is different It is propyl ester, tetrabutyl titanate, double(Ethyl acetoacetate)Metatitanic acid diisopropyl ester, the tert-butyl ester of metatitanic acid four, zinc acetate, the sulphur of dibutyl two For at least one in carbaminate, zinc dibutyl dithiophosphate, acetyl acetone, dibutyl dithio molybdenum phosphate.
The tackifier are di-t-butyl diacetyl oxosilane.
The deep layer adhesion promoters are many alkoxy silanes;Further, such as vinyltrimethoxy silane, vinyl three Ethoxysilane, MTMS, tetramethoxy-silicane, tetraethyl orthosilicate, γ-chloropropyl triethoxysilane, γ- R-chloropropyl trimethoxyl silane, γ-glycidyl ether oxygen propyl trimethoxy silicane, γ-methacryloxypropyl front three At least one in TMOS.
The preparation method of automotive electronics label silicon rubber bonder of the present invention is:First by 107 silicon rubber, benefit Strong filler distinguishes metered homogenizer, is warming up to 160 DEG C of dryings 20~30 minutes;Planetary mixer is then moved into take out very Idle discharge is steeped 30~60 minutes;Metered crosslinking agent, tackifier, deep layer adhesion promoters are pressed again, and 30 are mixed under vacuum ~60 minutes, finally metered catalyst, co-catalyst again, vacuum mixes 30~60 minutes, in the protection of inert gas Lower filtering is obtained final product in the PP pipes of isolation air.
Compared with prior art, the present invention has advantages below:
1st, the present invention is with hydroxyl-terminated injecting two methyl siloxane(107 glue), based on reinforced filling on the basis of sizing material, lead to Cross by crosslinking agent, catalyst, co-catalyst, tackifier, five kinds of auxiliary materials of deep layer adhesion promoters simultaneously compatibility use, especially with Viscosity is 107 silicon rubber, hydrophilic or the hydrophobic type fume colloidal silica polysiloxanes of 3000~20000mPaS for reinforcement is filled out Material, adds 1~8 part of crosslinking agent, 0.01~0.5 part of catalyst, 0.1~2 part of co-catalyst, thickening in 100 parts of sizings 0.5~5 part of agent, 0.1~2 part of deep layer adhesion promoters are formulated, the de- acetic acid type room temperature vulcanization silicon rubber of one-component of acquisition Glue, not only sizing material is easy to use, and has the advantages that curingprocess rate is fast, the high and low poison ring of transparency is protected, therefore as automobile electricity The binding agent of subtab, decapacitation is reached outside good performance requirement, while also having easy to operate, rapid link, viscose glue strong Degree effect high, 1 hour adhesive strength is 3~4 times of the usual silicone rubber under the conditions of.
2nd, the present invention can simultaneously assign sizing material existing excellent thixotropy using fume colloidal silica as reinforced filling, There is mechanicalness higher again.
3rd, the present invention is using containing zinc(Zn), titanium(Ti)Or molybdenum(Mo)Compound Deng element is co-catalyst, relatively common De- acetic acid type silicon rubber has faster curingprocess rate and deep layer vulcanization performance.
4th, it is deep layer adhesion promoters that the present invention uses many alkoxy silanes, and there is relatively common silicon rubber deep layer vulcanization to glue Performance and more preferable initial bonding strength are connect, good bonding can be formed to automotive electronics label in a short time, so that high degree On shorten set-up time of automotive electronics label.
5th, the preparation method of silicon rubber of the present invention is simple, and production equipment is conventional equipment, with short production cycle, and production process Middle three wastes are produced, environment-friendly.
In a word, using silicon rubber of the present invention as automotive electronics label bonding agent, compared with acrylate pressure-sensitive adhesive and ordinary silicon Rubber has more preferable adhesive strength, high-low temperature resistant, ultraviolet aging resistance and Anti-dismantling, is the popularization and application of automotive electronics label There is provided reliable guarantee.
Specific embodiment
With reference to embodiment, the present invention, but embodiments of the present invention not limited to this are expanded on further, it is all based on this hair The technology that bright the above is realized belongs to the scope of the present invention.
The testing standard and method of the indices foundation of silicon rubber bonder of the present invention be:
1st, mechanical property is characterized by the standard testing of GB defined:Wherein, tensile strength and elongation at break press GB/T 528- 2009th, Shore A hardness presses the method measure of GB/T 531-2008.
2nd, adhesive property tests ceramics-glass shear strength by the method for GB GB/T 7124-2008 defineds.
Embodiment 1
First by 85 parts of 107 silicon rubber of 5000mPaS viscosity, the specific surface area 200m of silazane treatment2The vapor phase method of/g is white 15 parts of carbon black, adds homogenizer, is warming up to 160 DEG C of dryings 30 minutes;Then move into planetary mixer and vacuumize row's bubble 45 Minute, add 3 parts of methyl triacetoxysilane, 2 parts of ethyltriacetoxysilane, di-t-butyl diacetyl silane 0.5 part, 1 part of vinyltrimethoxy silane mixes 30 minutes under vacuum, finally adds dibutyl tin dilaurate 0.02 part, 0.5 part of tetrabutyl titanate, vacuum mix 40 minutes, and the PP in isolation air is filtered under the protection of inert gas In pipe, automotive electronics label silicon rubber bonder is obtained final product.
Gained bonding agent is made mechanics and hardness test sample according to GB/T 528-2009, GB/T 531-2008 respectively Piece, vulcanizes 7 days under the conditions of 25 DEG C, relative humidity 50%, tests its tensile strength, elongation at break, Shao Er A hardness;According to GB/T 7124-2008 are made shearing sample, vulcanize 60 minutes under the conditions of 25 DEG C, relative humidity 50%, test it at 25 DEG C and Shear strength at a temperature of 100 DEG C, test result is shown in Table 1.
Embodiment 2
First by 88 parts of 107 silicon rubber of 10000mPaS viscosity, the specific surface area 200m of silazane treatment2The vapor phase method of/g is white 12 parts of carbon black, adds homogenizer, is warming up to 160 DEG C of dryings 30 minutes;Then move into planetary mixer and vacuumize row's bubble 40 Minute;Add 5 parts of ethyltriacetoxysilane, 1 part of di-t-butyl diacetyl silane, γ-glycidyl ether oxygen propyl 1.5 parts of trimethoxy silane, mixes 30 minutes under vacuum, finally adds 0.03 part of dibutyl tin acetate, metatitanic acid Four 0.8 part of isopropyl esters, vacuum mixes 60 minutes, is filtered under the protection of inert gas in the PP pipes of isolation air, obtains final product vapour Car electronic tag silicon rubber bonder.
Gained bonding agent is made mechanics and hardness test sample according to GB/T 528-2009, GB/T 531-2008 respectively Piece, vulcanizes 7 days under the conditions of 25 DEG C, relative humidity 50%, tests its tensile strength, elongation at break, Shao Er A hardness;According to GB/T 7124-2008 are made shearing sample, vulcanize 60 minutes under the conditions of 25 DEG C, relative humidity 50%, test it at 25 DEG C and Shear strength at a temperature of 100 DEG C, test result is shown in Table 1.
Embodiment 3
First by 85 parts of 107 silicon rubber of 5000mPaS viscosity, the specific surface area 200m of silazane treatment2The vapor phase method of/g is white 15 parts of carbon black, adds homogenizer, is warming up to 160 DEG C of dryings 30 minutes;Then move into planetary mixer and vacuumize row's bubble 45 Minute;Add 2 parts of vinyltriacetoxy silane, 3 parts of ethyltriacetoxysilane, di-t-butyl diacetyl silane 1 part, 0.8 part of tetraethyl orthosilicate, under vacuum mix 30 minutes, finally add 0.02 part of dibutyl tin dilaurate, 0.3 part of acetyl acetone, vacuum mixes 60 minutes, is filtered under the protection of inert gas in the PP pipes of isolation air, obtains final product Automotive electronics label silicon rubber bonder.
Gained bonding agent is made mechanics and hardness test sample according to GB/T 528-2009, GB/T 531-2008 respectively Piece, vulcanizes 7 days under the conditions of 25 DEG C, relative humidity 50%, tests its tensile strength, elongation at break, Shao Er A hardness;According to GB/T 7124-2008 are made shearing sample, vulcanize 60 minutes under the conditions of 25 DEG C, relative humidity 50%, test it at 25 DEG C and Shear strength at a temperature of 100 DEG C, test result is shown in Table 1.
Embodiment 4
First by 82 parts of the 107 silicon rubber of 8000mPaS viscosity, the specific surface area 150m of silazane treatment2The vapor phase method hard charcoal of/g Black 18 parts, homogenizer is added, be warming up to 160 DEG C of dryings 30 minutes;Then move into planetary mixer and vacuumize 50 points of row's bubble Clock;Add 3.5 parts of methyl triacetoxysilane, 1.5 parts of propyl group triacetoxysilane, di-t-butyl diacetyl silane 0.5 part, 1 part of vinyltrimethoxy silane, 0.5 part of γ-r-chloropropyl trimethoxyl silane mix 30 points under vacuum Clock, finally adds 0.05 part of dibutyl tin dioctoate, double(Ethyl acetoacetate)0.5 part of metatitanic acid diisopropyl ester, dibutyl two 0.3 part of D2EHDTPA zinc, vacuum mixes 60 minutes, is filtered under the protection of inert gas in the PP pipes of isolation air, obtains final product Automotive electronics label silicon rubber bonder.
Gained bonding agent is made mechanics and hardness test sample according to GB/T 528-2009, GB/T 531-2008 respectively Piece, vulcanizes 7 days under the conditions of 25 DEG C, relative humidity 50%, tests its tensile strength, elongation at break, Shao Er A hardness;According to GB/T 7124-2008 are made shearing sample, vulcanize 60 minutes under the conditions of 25 DEG C, relative humidity 50%, test it at 25 DEG C and Shear strength at a temperature of 100 DEG C, test result is shown in Table 1.
Embodiment 5
First by 85 parts of the 107 silicon rubber of 10000mPaS viscosity, the specific surface area 150m of silazane treatment2The vapor phase method hard charcoal of/g Black 15 parts, homogenizer is added, be warming up to 160 DEG C of dryings 30 minutes;Then move into planetary mixer and vacuumize 50 points of row's bubble Clock;Add 3.5 parts of methyl triacetoxysilane, 1.5 parts of vinyltriacetoxy silane, di-t-butyl diacetyl silane 1 part, 1 part of tetramethoxy-silicane, 0.5 part of γ-methacryloxypropyl trimethoxy silane mix 30 under vacuum Minute, finally add 0.05 part of dibutyl tin dioctoate, 0.5 part of dibutyl dithio molybdenum phosphate, dibutyl dithio phosphoric acid 0.5 part of zinc, vacuum mixes 60 minutes, is filtered under the protection of inert gas in the PP pipes of isolation air, obtains final product automotive electronics Label silicon rubber bonder.
Gained bonding agent is made mechanics and hardness test sample according to GB/T 528-2009, GB/T 531-2008 respectively Piece, vulcanizes 7 days under the conditions of 25 DEG C, relative humidity 50%, tests its tensile strength, elongation at break, Shao Er A hardness;According to GB/T 7124-2008 are made shearing sample, vulcanize 60 minutes under the conditions of 25 DEG C, relative humidity 50%, test it at 25 DEG C and Shear strength at a temperature of 100 DEG C, test result is shown in Table 1.
Embodiment 6
First by 70 parts of 107 silicon rubber of 3000mPaS viscosity, the specific surface area 300m of silazane treatment2The vapor phase method of/g is white 30 parts of carbon black, adds homogenizer, is warming up to 160 DEG C of dryings 20 minutes;Then move into planetary mixer and vacuumize row's bubble 60 Minute;2 parts of methyl triacetoxysilane, 3 parts of ethyltriacetoxysilane, 3 parts of propyl group triacetoxysilane are added, 3 parts of di-t-butyl diacetyl silane, 1 part of vinyltrimethoxy silane, 1 part of MTMS, in vacuum condition Lower mixing 60 minutes, finally adds 0.01 part of dibutyl tin dilaurate, 1 part of tetrabutyl titanate, 1 part of zinc acetate, vacuum Mixing 50 minutes, filters in the PP pipes of isolation air under the protection of inert gas, obtains final product automotive electronics label silicon rubber Bonding agent.
Gained bonding agent is made mechanics and hardness test sample according to GB/T 528-2009, GB/T 531-2008 respectively Piece, vulcanizes 7 days under the conditions of 25 DEG C, relative humidity 50%, tests its tensile strength, elongation at break, Shao Er A hardness;According to GB/T 7124-2008 are made shearing sample, vulcanize 60 minutes under the conditions of 25 DEG C, relative humidity 50%, test it at 25 DEG C and Shear strength at a temperature of 100 DEG C, test result is shown in Table 1.
Embodiment 7
First by 80 parts of 107 silicon rubber of 20000mPaS viscosity, the specific surface area 100m of silazane treatment2The vapor phase method of/g is white 20 parts of carbon black, adds homogenizer, is warming up to 160 DEG C of dryings 30 minutes;Then move into planetary mixer and vacuumize row's bubble 30 Minute;Add 1 part of ethyltriacetoxysilane, 5 parts of di-t-butyl diacetyl silane, MTMS 0.1 Part, mix 40 minutes under vacuum, 0.5 part of dibutyl tin dilaurate, 0.1 part of tetraisopropyl titanate are finally added, Vacuum mixes 30 minutes, is filtered under the protection of inert gas in the PP pipes of isolation air, obtains final product automotive electronics label silicon Rubber adhesive.
Gained bonding agent is made mechanics and hardness test sample according to GB/T 528-2009, GB/T 531-2008 respectively Piece, vulcanizes 7 days under the conditions of 25 DEG C, relative humidity 50%, tests its tensile strength, elongation at break, Shao Er A hardness;According to GB/T 7124-2008 are made shearing sample, vulcanize 60 minutes under the conditions of 25 DEG C, relative humidity 50%, test it at 25 DEG C and Shear strength at a temperature of 100 DEG C, test result is shown in Table 1.
Embodiment 8
First by 75 parts of 107 silicon rubber of 15000mPaS viscosity, the specific surface area 250m of silazane treatment2The vapor phase method of/g is white 25 parts of carbon black, adds homogenizer, is warming up to 160 DEG C of dryings 20 minutes;Then move into planetary mixer and vacuumize row's bubble 50 Minute;Add 1 part of ethyltriacetoxysilane, 2 parts of propyl group triacetoxysilane, di-t-butyl diacetyl silane 2 Part, 0.5 part of γ-methacryloxypropyl trimethoxy silane, mix 35 minutes under vacuum, finally add two 0.2 part of butyl tin dilaurate tin, 0.1 part of dibutyl tin acetate, 0.5 part of tetraisopropyl titanate, dibutyl dithio molybdenum phosphate 1 Part, vacuum mixes 45 minutes, is filtered under the protection of inert gas in the PP pipes of isolation air, obtains final product automotive electronics label use Silicon rubber bonder.
Gained bonding agent is made mechanics and hardness test sample according to GB/T 528-2009, GB/T 531-2008 respectively Piece, vulcanizes 7 days under the conditions of 25 DEG C, relative humidity 50%, tests its tensile strength, elongation at break, Shao Er A hardness;According to GB/T 7124-2008 are made shearing sample, vulcanize 60 minutes under the conditions of 25 DEG C, relative humidity 50%, test it at 25 DEG C and Shear strength at a temperature of 100 DEG C, test result is shown in Table 1.
Comparative example 1(It is not added with co-catalyst, deep layer adhesion promoters)
First by 85 parts of the 107 silicon rubber of 5000mPaS viscosity, the specific surface area 200m of silazane treatment2The vapor phase method hard charcoal of/g Black 15 parts, homogenizer is added, be warming up to 160 DEG C of dryings 30 minutes;Then move into planetary mixer and vacuumize 45 points of row's bubble Clock;5 parts of methyl triacetoxysilane, 1 part of di-t-butyl diacetyl silane are added, 30 points are mixed under vacuum Clock, finally adds 0.02 part of dibutyl tin dilaurate, and vacuum mixes 60 minutes, filtered under the protection of inert gas Completely cut off in the PP pipes of air, obtain final product silicon rubber bonder.
Gained bonding agent is made mechanics and hardness test sample according to GB/T 528-2009, GB/T 531-2008 respectively Piece, vulcanizes 7 days under the conditions of 25 DEG C, relative humidity 50%, tests its tensile strength, elongation at break, Shao Er A hardness;According to GB/T 7124-2008 are made shearing sample, vulcanize 60 minutes under the conditions of 25 DEG C, relative humidity 50%, test it at 25 DEG C and Shear strength at a temperature of 100 DEG C, test result is shown in Table 1.
Comparative example 2(It is not added with co-catalyst, deep layer adhesion promoters)
First by 82 parts of the 107 silicon rubber of 8000mPaS viscosity, the specific surface area 150m of silazane treatment2The vapor phase method hard charcoal of/g Black 18 parts, homogenizer is added, be warming up to 160 DEG C of dryings 30 minutes;Then move into planetary mixer and vacuumize 45 points of row's bubble Clock;Add 3 parts of methyl triacetoxysilane, 2 parts of ethyltriacetoxysilane, 1 part of di-t-butyl diacetyl silane, Mix 30 minutes under vacuum, finally add 0.02 part of dibutyl tin dilaurate, vacuum mixes 60 minutes, lazy Property gas protection under filter isolation air PP pipe in, obtain final product silicon rubber bonder.
Gained bonding agent is made mechanics and hardness test sample according to GB/T 528-2009, GB/T 531-2008 respectively Piece, vulcanizes 7 days under the conditions of 25 DEG C, relative humidity 50%, tests its tensile strength, elongation at break, Shao Er A hardness;According to GB/T 7124-2008 are made shearing sample, vulcanize 60 minutes under the conditions of 25 DEG C, relative humidity 50%, test it at 25 DEG C and Shear strength at a temperature of 100 DEG C, test result is shown in Table 1.
Comparative example 3(Acrylate pressure-sensitive adhesive)
By 3M companies VHB-4595 type double faced adhesive tapes, shearing sample is made according to GB/T 7124-2008, in 25 DEG C, relative humidity It is bonded respectively under the conditions of 50% 30,60 minutes, tests its shear strength at a temperature of 25 DEG C and 100 DEG C, the results are shown in Table 1.
Be can be seen that from table 1:
Although the 1, embodiment 1-8 and comparative example 1, the test result of comparative example 2, do not have too big difference in mechanical property, The shear strength of 30min, 60min(Ceramics-glass), embodiment 1-8 is 3~4 times of comparative example, shows to be developed using the present invention Automotive electronics label silicon rubber bonder can significantly shorten set-up time of automotive electronics label first, will be original several small When set-up time foreshorten to 30~60 minutes, drastically increase the installation effectiveness of electronic tag;Secondly silicon rubber 30~ Initial bonding strength in 60min is greatly improved, and can prevent automotive electronics label from artificially being pulled down at the installation initial stage, changed.
Although the 2, comparative example 3 bonding initially just have certain initial adhesive strength, its shear strength be bonded the time extension Vary less, but when temperature rises to 100 DEG C, the adhesive strength of comparative example 3 then can sharp-decay, show using appropriate heater Tool can easily, intactly remove the automotive electronics label that acrylate pressure-sensitive adhesive is bonded, and change to other vehicles or will be with original The unmatched electronic tag of vehicle is attached to the vehicle, and " one-car-one-card " principle when this sets up with automotive electronics label is disagreed The back of the body, the management in the future to automotive electronics label is extremely disadvantageous.
Embodiment described above is of the invention only for preferably illustrating, and the scope being not intended to limit the invention, all bases Any modification, equivalent, improvement made in the above of the present invention etc., each falls within the scope of the present invention.

Claims (10)

1. a kind of automotive electronics label silicon rubber bonder, it is characterised in that:Raw material includes sizing and auxiliary material, described auxiliary Expect that the addition weight with 100 parts of sizings as weight basis is:
1~8 part of crosslinking agent
0.01~0.5 part of catalyst
0.1~2 part of co-catalyst
0.5~5 part of tackifier
0.1~2 part of deep layer adhesion promoters
The sizing includes 70~88 parts of hydroxyl-terminated injecting two methyl siloxane, the reinforced filling 12~30 counted by weight Part.
2. a kind of automotive electronics label silicon rubber bonder according to claim 1, it is characterised in that:The terminal hydroxy group Dimethyl silicone polymer is one kind or any several mixing in the polysiloxanes of 3000~20000mPaS selected from viscosity Thing.
3. a kind of automotive electronics label silicon rubber bonder according to claim 1, it is characterised in that:The reinforcement is filled out Expect to be hydrophilic or hydrophobic type fume colloidal silica.
4. a kind of automotive electronics label silicon rubber bonder according to claim 1 or 3, it is characterised in that:The benefit Strong filler is the 100~300m of specific surface area of silazane treatment2The hydrophobic type fume colloidal silica of/g.
5. a kind of automotive electronics label silicon rubber bonder according to claim 1, it is characterised in that:The crosslinking agent It is methyl triacetoxysilane, ethyltriacetoxysilane, propyl group triacetoxysilane, vinyl triacetoxy silicon At least one in alkane.
6. a kind of automotive electronics label silicon rubber bonder according to claim 1, it is characterised in that:The catalyst It is at least one in dibutyl tin dilaurate, dibutyl tin dioctoate, dibutyl tin acetate.
7. a kind of automotive electronics label silicon rubber bonder according to claim 1, it is characterised in that:The co-catalysis Agent is the compound containing zinc, titanium or molybdenum element, including:It is tetraisopropyl titanate, tetrabutyl titanate, double(Ethyl acetoacetate)Titanium Sour diisopropyl ester, the tert-butyl ester of metatitanic acid four, zinc acetate, zinc dibutyl dithiocarbamate, zinc dibutyl dithiophosphate, acetyl At least one in acetone molybdenum, dibutyl dithio molybdenum phosphate.
8. a kind of automotive electronics label silicon rubber bonder according to claim 1, it is characterised in that:The tackifier It is di-t-butyl diacetyl oxosilane.
9. a kind of automotive electronics label silicon rubber bonder according to claim 1, it is characterised in that:The deep layer is glued Accelerator is connect for many alkoxy silanes, including:Vinyltrimethoxy silane, VTES, methyl trimethoxy oxygen Base silane, tetramethoxy-silicane, tetraethyl orthosilicate, γ-chloropropyl triethoxysilane, γ-r-chloropropyl trimethoxyl silane, In γ-glycidyl ether oxygen propyl trimethoxy silicane, γ-methacryloxypropyl trimethoxy silane at least one Kind.
10. a kind of automotive electronics label silicon rubber bonder as described in any one in claim 1-9, its feature are prepared It is that specific method is:107 silicon rubber, reinforced filling are first distinguished into metered homogenizer, 160 DEG C of dryings are warming up to 20~30 minutes;Then move into planetary mixer and vacuumize row's bubble 30~60 minutes;Again by metered crosslinking agent, tackifier, Deep layer adhesion promoters, mix 30~60 minutes under vacuum, finally metered catalyst, co-catalyst, vacuum again Mixing 30~60 minutes, filters under the protection of inert gas and is obtained final product in the PP pipes of isolation air.
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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107286668A (en) * 2017-08-03 2017-10-24 泉州市知产茂业工业设计有限公司 Acid silicon rubber of a kind of double component room temperature vulcanization and preparation method thereof
CN108395868A (en) * 2018-01-31 2018-08-14 苏州达同新材料有限公司 The special two-component casting glue of photovoltaic junction box
JP2019533747A (en) * 2016-10-31 2019-11-21 ワッカー ケミー アクチエンゲゼルシャフトWacker Chemie AG Single component room temperature curable compositions based on organosilicon compounds and titanium curing catalysts
CN110511719A (en) * 2019-08-02 2019-11-29 中国航发北京航空材料研究院 One pack system high intensity depickling type room temperature vulcanized organosilicon sealant and preparation method thereof
CN111334245A (en) * 2020-04-16 2020-06-26 中科新镧系(厦门)科技有限公司 Dealcoholized excellent-yellowing-resistance organosilicon sealant and preparation method thereof
CN111394054A (en) * 2020-03-24 2020-07-10 新安天玉有机硅有限公司 Silicone rubber for self-adhesive tape and preparation method thereof
CN112778965A (en) * 2019-11-11 2021-05-11 中蓝晨光化工研究设计院有限公司 Alcohol-type silicon rubber adhesive and preparation method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002097440A (en) * 2000-09-21 2002-04-02 Shin Etsu Chem Co Ltd Silicone adhesive composition
CN102277127A (en) * 2011-08-05 2011-12-14 曾庆铭 Acidic silicone sealant
CN103319900A (en) * 2013-06-07 2013-09-25 浙江汇杰有机硅有限公司 High-transparency room-temperature-cured silicone composition and preparation method thereof
CN103788914A (en) * 2013-12-26 2014-05-14 李泽国 Anti-algae silicone adhesive and preparation method thereof
CN104263315A (en) * 2014-09-28 2015-01-07 浙江时间新材料有限公司 Acidic and transparent silicone weather-resistant sealant for construction

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002097440A (en) * 2000-09-21 2002-04-02 Shin Etsu Chem Co Ltd Silicone adhesive composition
CN102277127A (en) * 2011-08-05 2011-12-14 曾庆铭 Acidic silicone sealant
CN103319900A (en) * 2013-06-07 2013-09-25 浙江汇杰有机硅有限公司 High-transparency room-temperature-cured silicone composition and preparation method thereof
CN103788914A (en) * 2013-12-26 2014-05-14 李泽国 Anti-algae silicone adhesive and preparation method thereof
CN104263315A (en) * 2014-09-28 2015-01-07 浙江时间新材料有限公司 Acidic and transparent silicone weather-resistant sealant for construction

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
邝生鲁等: "《现代精细化工高新技术与产品合成工艺》", 31 December 1997, 科学技术文献出版社 *

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2019533747A (en) * 2016-10-31 2019-11-21 ワッカー ケミー アクチエンゲゼルシャフトWacker Chemie AG Single component room temperature curable compositions based on organosilicon compounds and titanium curing catalysts
CN107286668A (en) * 2017-08-03 2017-10-24 泉州市知产茂业工业设计有限公司 Acid silicon rubber of a kind of double component room temperature vulcanization and preparation method thereof
CN108395868A (en) * 2018-01-31 2018-08-14 苏州达同新材料有限公司 The special two-component casting glue of photovoltaic junction box
CN110511719A (en) * 2019-08-02 2019-11-29 中国航发北京航空材料研究院 One pack system high intensity depickling type room temperature vulcanized organosilicon sealant and preparation method thereof
CN112778965A (en) * 2019-11-11 2021-05-11 中蓝晨光化工研究设计院有限公司 Alcohol-type silicon rubber adhesive and preparation method thereof
CN111394054A (en) * 2020-03-24 2020-07-10 新安天玉有机硅有限公司 Silicone rubber for self-adhesive tape and preparation method thereof
CN111334245A (en) * 2020-04-16 2020-06-26 中科新镧系(厦门)科技有限公司 Dealcoholized excellent-yellowing-resistance organosilicon sealant and preparation method thereof

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