CN105331116A - One-component heating-cured liquid silicone rubber and preparation method thereof - Google Patents
One-component heating-cured liquid silicone rubber and preparation method thereof Download PDFInfo
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Abstract
The invention belongs to the field of liquid silicone rubber and particularly relates to one-component heating-cured liquid silicone rubber and a preparation method thereof. According to the one-component heating-cured liquid silicone rubber, vinyl polysiloxane is taken as base rubber, hydrogen-based polysiloxane is taken as a cross-linking agent, a complex of transition metal platinum is taken as a catalyst, an alkynol mixture is taken as a high-efficiency polymerization inhibitor, aluminum oxide and aluminum nitride are taken as heat conducting filler, a silane coupling agent is taken as a thickening agent, aluminum hydroxide is taken as a fire retardant, and fumed silica is taken as a reinforcing agent. Technologically, strict control is adopted, a process route that raw materials are preprocessed and dried and then are subjected to rubber preparation after normal-temperature mixing is adopted, and the one-component heating-cured liquid silicone rubber is prepared. The one-component heating-cured liquid silicone rubber can be stored at the normal temperature for long time, is low in viscosity, good in heat conductivity, good in temperature endurance and good in substrate adhesion property and has one component and flame retardancy.
Description
Technical field
The invention belongs to field of liquid silicone rubber, particularly relate to a kind of single-component and to be heating and curing liquid silicon
Rubber and preparation method thereof.
Background technology
Silicon rubber is a kind of have excellent electrical property and unreactiveness, heat-resisting, ageing-resistant, moisture-proof, ventilative, elastic macromolecular material can be kept for a long time within the scope of-60 ~ 200 DEG C, wherein add-on type cure silicone rubber can realize fast setting at relatively high temperatures, machine-shaping is convenient, easily be automated, save the energy and labor force, be widely used in automatic production process.
Single-component silicon rubber is divided into condensed type single-component silicon rubber and add-on type single-component silicon rubber, wherein condensed type single-component silicon rubber only can self-vulcanizing, use exists solidification slow, can not inside and outside solidify simultaneously, in sulfidation shrinking percentage large, have the shortcomings such as by product generation.In contrast to this, add-on type single-component silicon rubber is by heating fast setting, and in sulfidation, shrinkability is minimum, and the inside and outside deep cure of energy, vulcanization rate and ambient moisture have nothing to do, and have the features such as excellent high thermal resistance.
Common single-component add-on type liquid silicon rubber, be take vinyl polysiloxane as base glue, hydrogen based polysiloxane is linking agent, and platinum complex is catalyzer, and single alkynol class, as stopper, adds filler formulated.There is following shortcoming in this product: in production in production and application, the filler added on heat-resisting, heat conductivility and product viscosity impact large, adding too much filler makes viscosity raise, and thixotropy is large, and after placing for some time, viscosity reduces and makes troubles to production control; In application aspect: when 1, using as sealing agent or tackiness agent, not easily peel off the bonding strength of base material; 2, heat conductivility better, excellent in flame retardance and the good product viscosity of intensity is higher, be not suitable for operation.3, product shelf characteric is bad, and the normal temperature storage phase is no more than 6 months, the shelf-time more than 6 months after, use properties declines, can direct sulfuration time serious, can not use.4, long-term
Resistance to elevated temperatures is general.The defects such as the bulk strength of silicon rubber is lower, and can reach the object of high strength by adding reinforced filling, but there is poor fluidity, normal temperature not easily stores, bonding force difference.Along with the development of electronic product, the demand of enhancing productivity further is more and more higher, and the be heating and curing exploitation of silicon rubber of the low viscosity single-component with good fluidity necessitates.And along with the development of science and technology, electronic product applies to, in the life of people, work, in order to reach satisfied performance, need the silica gel special with following character more and more:
1, the thermal conductivity required for using is met: along with the development of microelectronics and large-scale integrated circuit, circuit components high concentration, the heat radiation of components and parts becomes distinct issues, directly has influence on equipment and the reliability of used various high precise equipments.If the heat produced can not conduct in time, easily form localized hyperthermia, thermally conductive and electrically insulating silicone rubber has good heat-sinking capability, the heat of generation is conducted in time, not easily form localized hyperthermia, prevent the damage to appliance component, thus improve the reliability of system.Should select for reaching requirement product the filler that thermal conductivity is higher, can greatly be improved by heat conductivility after the agent treated such as silazane simultaneously.
2, viscosity is low: lower viscosity is more conducive to operation, especially when being applied in sealing protection.
3, can fast setting under heating: as production line balance operation, for ensureing working efficiency, need this kind of silica gel special can in a heated condition can fast setting, if can not fast setting, the waste of plenty of time in workflow can be caused, affect production efficiency.
4, cementability: in order to ensure that product has excellent moisture sealed effect, need there is good adhesiveproperties between silica gel and base material.Adopt silane coupling agent to improve the cementability of product, substantially increase the bonding strength of silica gel to base material.
5, product storage-stable: single-component silicon rubber wishes can have good mobility at normal temperatures, easy handling uses, and simultaneously the longer the better lower storage time for normal temperature.The general single-component silicon rubber normal temperature that is heating and curing is shorter for storage time, all adopts low temperature to store.
So, when developing single-component silicon rubber, need to solve composition and engineering two problems, product mobility can either be made suitable, good to substrate bonding power, product fast setting can be made again, final product has: viscosity is low, thermal conductivity good, temperature tolerance is good, good flame-retardance, good bonding, the characteristic such as environment friendly and pollution-free, meet the need of market.
Summary of the invention
For solving above technical problem, the present invention is directed to the demand being applied in electron trade, fast setting, high strength after a low viscosity developed, heating, with substrate bonding is good, thermal conductivity is good, temperature tolerance is good, excellent in flame retardance, the add-on type single-component of long storage periods is heating and curing the invention of liquid silastic product at normal temperatures.
The present invention uses vinyl polysiloxane for base glue, hydrogen based polysiloxane is linking agent, the complex compound of metal platinum is as catalyzer, alkynes alcohol-based mixtures is as high-efficiency polymerization inhibitor, aluminum oxide and aluminium nitride are as heat conductive filler, silane coupling agent is as tackifier, and aluminium hydroxide is fire retardant, and thermal silica is strengthening agent.In technique, by strict control, raw material is taked to anticipate drying,
A kind of single-component that the present invention solves above technical problem is heating and curing liquid silastic, in its formula, each component weight part is: vinyl polysiloxane 100 parts, aluminum oxide 50-100 part, aluminium nitride 50-80 part, aluminium hydroxide 30-50 part and 10-20 part thermal silica, with according to above base glue, heat conductive filler, fire retardant, strengthening agent total mass part 100 parts calculated hydrogen based polysiloxane 3-6 part, silane coupling agent 0.5-2 part, platinum complex 0.05-0.2 part, alkynol class stopper 0.01-0.02 part.
Use silane coupling agent to make tackifier, improve silicon rubber to the cementability of base material; Aluminium nitride is conventional high-efficiency heat conduction filler, but with high costs because of it, is difficult to widely apply in general industry product.The present invention adopts aluminum oxide and aluminium nitride with the use of making heat conductive filler, not only can be cost-saving, significantly can also be improved the heat conductivility of silicon rubber by the collocation of particle diameter.
In the present invention, described aluminum oxide and aluminium nitride for obtain after octamethylcyclotetrasiloxane and silazane pre-treatment, and the treatment step of aluminum oxide, aluminium nitride or aluminium hydroxide is as follows:
Add 100 parts of aluminum oxide of weight part in a kettle., stir while add the octamethylcyclotetrasiloxane of 5-10 part, stir, then add the hexamethyldisilazane of 5-20 part, heat up under nitrogen flowing, keep 80-120 DEG C and be uniformly mixed 2-4h, naturally cooling, after placing 6-12 hour, reheats to 150-180 DEG C at 18-25 DEG C, dry 4-5 hour, namely obtains the alumina packing after processing after cooling.The treatment step of aluminium nitride or aluminium hydroxide is the same with process aluminum oxide.
Carry in high performance process at silicon rubber, filler add the rapid rising that membership causes silicon rubber viscosity, in order to ensure the viscosity of product, often the add-on of filler is subject to certain restrictions.But filler after treatment, its surface can be transformed into lipophilicity by wetting ability, thus has the better consistency with silicon rubber, thus reduces the viscosity of system.In order to increase the wetness degree of filling surface, adopt octamethylcyclotetrasiloxane and hexamethyldisilazane pretreated filler that the consistency of filler and base glue can be made better, can when the equal filler of interpolation, improve the filling ratio of filler in base glue and reduce system viscosity, can reduce system viscosity on the basis making product obtain other excellent properties, this process simultaneously contributes to improving product thermal conductivity.
The viscosity of described vinyl polysiloxane is selected within the scope of 500-50000mpa.s.
Described silane coupling agent can be vinyltriethoxysilane, vinyltrimethoxy silane or γ-(2,3-epoxy third oxygen) propyl trimethoxy silicane.
Described alkynol class stopper is butynol and hexamethylene alkynol.Alkynol class mixed inhibitor is adopted to extend the normal temperature storage time of product, and the storage stability of product.
The consumption of described alkynol class stopper is 0.005-0.01 part butynol and 0.005-0.01 part hexamethylene alkynol.
A kind of Single-component low-viscosity high strength bonding silicon rubber preparation method in the present invention, is characterized in that:
Step (1): vinyl polysiloxane 100 parts, aluminum oxide 50-100 part, aluminium nitride 50-80 part, aluminium hydroxide 30-50 part and 10-20 part thermal silica join in kneader, stir, be warming up to 130-160 DEG C, vacuumize and stir after 2-6 hour, take out, three-roller is milled 1-2 time, obtains sizing;
Step (2): get sizing 100 parts and stir in planet still, add the hydrogen based polysiloxane 3-6 part obtained according to added sizing quality deal, silane coupling agent tackifier 0.5-2 part, alkynol class stopper 0.01-0.02 part, after stirring, add the full thing catalyzer of network of 0.05-0.2 part transition metal platinum, stir 2-4 hour;
Step (3): filter, pack and obtain single-component and to be heating and curing silicon rubber.
As the preferred version in the present invention, described silane coupling agent tackifier can obtain according to following steps:
Tetramethyl-tetrahydrochysene cyclotetrasiloxane, vinyltriethoxysilane are mixed by quality mol ratio 1:1-2, add the platinum catalyst of total mass percentage composition 1-2 ‰, 12-24h is reacted at 20-30 DEG C, be warmed up to 80-100 DEG C of reaction 2-4h again, finally be warmed up to 120-150 DEG C of reaction 2-4 hour, filter after normal temperature naturally cooling, obtain tackifier.
Addition-type silicon rubber is because polarity own is poor, always poor with the bonding force of base material.Although cementability to base material can be improved to a certain extent by adding general silane coupling agent, but there is product and store hydrolysis because of silane coupling agent after for some time, the problem that bonding strength declines.
Silane coupling agent obtained in preferred version of the present invention and addition-type silicon rubber have excellent compatibility, as tackifier, can, while the stability ensureing silicon rubber, make silicon rubber have good bonding force and permanent stability to base material.
The present invention is completed by following reaction mechanism:
The oligoorganosiloxanes containing more than 3 Si-H groups in a kind of molecule is adopted to be linking agent, under the effect of catalyzer, the Si-H key addition reaction of the vinyl-functional in vinyl polysiloxane and hydrogen based polysiloxane, finally be formed with the cross-linked network of organosilicon polymer, realize the cross-linking vulcanized of silicon rubber.By adding filler, silicon rubber can be made to have special performance, as flame retardant resistance, thermal conductivity etc.
The invention belongs to add-on type cure silicone rubber, therefore needing in a heated condition can fast setting, requires that at room temperature having sufficiently long obtains the operating time simultaneously, therefore needs when selecting catalyzer and stopper to consider kind and consumption.The present invention selects active higher platinum catalyst, and the stopper that can volatilize fast under Elevated Temperature Conditions while that inhibition being better at ambient temperature, reaches the object of technical solution problem.Be heating and curing and refer to that normal temperature can not solidify, must heat and could consolidate
The present invention be can at normal temperatures prolonged storage, low viscosity, single-component, thermal conductivity is good, temperature tolerance is good, be heating and curing with the good flame retardant resistance single-component of substrate bonding liquid silastic, meets required requirement on market.
For handling characteristics and the specification of quality of the single component liquid silicon rubber required for electron trade, a kind of single-component provided by the invention is heating and curing liquid silastic, has low viscosity (viscosity≤60Pa.s/25 DEG C); Fast setting (130 DEG C × 1 hour curable); High strength (tensile strength >=2.5Mpa); Excellent bonding force good (shearing resistance >=2.2Mpa), good thermal conductivity (thermal conductivity >=1.0w/m.k), flame retardant resistance is UL-94V0 level, excellent temperature tolerance (can use under 250 DEG C of conditions for a long time), and can normal temperature storage more than 12 months.
Embodiment
Embodiment 1
By vinyl polysiloxane 100 parts, 50 parts, pre-treatment rear oxidation aluminium, aluminium nitride 50 parts, 30 parts, aluminium hydroxide and 10 parts of thermal silicas join in kneader, stir, are warming up to 130 DEG C, vacuumize stirring after 2 hours, take out, three-roller is milled 1 time, obtain the uniform sizing of fillers dispersed.
Get sizing 100 parts to stir in planet still, add the hydrogen based polysiloxane 3 parts obtained according to added sizing quality deal, tackifier vinyltriethoxysilane 0.5 part, 0.005 part of butynol and 0.005 hexamethylene alkynol, after stirring, add 0.05 part of platinum complex catalyst, stir 2 hours.Filter and package and can be mixed with single-component and to be heating and curing silicon rubber.
Wherein, the pre-treatment of filler (comprising aluminum oxide, aluminium nitride or aluminium hydroxide)
Add 100 parts of (mass parts, as follows) aluminum oxide, aluminium nitride or filling aluminium hydrates in a kettle., stir the octamethylcyclotetrasiloxane adding 5 parts, stir, add the hexamethyldisilazane of 5 parts again, under N2 air-flow, heat up, keep 100 DEG C and be uniformly mixed 3h, naturally cooling, after normal temperature places 12 hours, reheats to 150 DEG C, dry 4 hours, after cooling, namely obtain the filler after processing.
Embodiment 2
By vinyl polysiloxane 100 parts, 100 parts, pre-treatment rear oxidation aluminium, aluminium nitride 80 parts, 50 parts, aluminium hydroxide and 20 parts of thermal silicas join in kneader, stir, are warming up to 160 DEG C, vacuumize stirring after 6 hours, take out, three-roller is milled 2 times, obtain the uniform sizing of fillers dispersed.
Get sizing 100 parts to stir in planet still, add the hydrogen based polysiloxane 6 parts obtained according to added sizing quality deal, vinyltrimethoxy silane tackifier 2 parts, 0.01 part of butynol and 0.01 part of hexamethylene alkynol, after stirring, add 0.2 part of platinum complex catalyst, stir 4 hours.Filter and package and can be mixed with single-component and to be heating and curing silicon rubber.
The pre-treatment of filler (comprising aluminum oxide, aluminium nitride or aluminium hydroxide)
Add 100 parts of (mass parts, as follows) aluminum oxide, aluminium nitride or filling aluminium hydrates in a kettle., stir the octamethylcyclotetrasiloxane adding 10 parts, stir, add the hexamethyldisilazane of 20 parts again, under N2 air-flow, heat up, keep 120 DEG C and be uniformly mixed 3h, naturally cooling, after normal temperature places 12 hours, reheats to 150 DEG C, dry 4 hours, after cooling, namely obtain the filler after processing.
Embodiment 3
By vinyl polysiloxane 100 parts, 80 parts, pre-treatment rear oxidation aluminium, aluminium nitride 70 parts, 40 parts, aluminium hydroxide and 15 parts of thermal silicas join in kneader, stir, are warming up to 150 DEG C, vacuumize stirring after 5 hours, take out, three-roller is milled 1 time, obtain the uniform sizing of fillers dispersed.
Get sizing 100 parts to stir in planet still, add the hydrogen based polysiloxane 5 parts obtained according to added sizing quality deal, γ-(2,3-epoxy third oxygen) propyl trimethoxy silicane tackifier 1.5 parts, 0.008 part of butynol and 0.007 part of hexamethylene alkynol, after stirring, add 0.1 part of platinum complex catalyst, stir 3 hours.Filter and package and can be mixed with single-component and to be heating and curing silicon rubber.
The pre-treatment of filler (comprising aluminum oxide, aluminium nitride or aluminium hydroxide)
Add 100 parts of (mass parts, as follows) aluminum oxide, aluminium nitride or filling aluminium hydrates in a kettle., stir the octamethylcyclotetrasiloxane adding 7 parts, stir, add the hexamethyldisilazane of 10 parts again, under N2 air-flow, heat up, keep 80 DEG C and be uniformly mixed 3h, naturally cooling, after normal temperature places 12 hours, reheats to 150 DEG C, dry 4 hours, after cooling, namely obtain the filler after processing.
Embodiment 4
By vinyl polysiloxane 100 parts, 90 parts, pre-treatment rear oxidation aluminium, aluminium nitride 60 parts, aluminium hydroxide 45 parts of 18 parts of thermal silicas join in kneader, stir, are warming up to 140 DEG C, vacuumize stirring after 4 hours, take out, three-roller is milled 2 times, obtain the uniform sizing of fillers dispersed.
Get sizing 100 parts to stir in planet still, add the hydrogen based polysiloxane 4 parts obtained according to added sizing quality deal, vinyltrimethoxy silane tackifier 1 part, 0.008 part of butynol and 0.01 part of hexamethylene alkynol, after stirring, add 0.15 part of platinum complex catalyst, stir 3 hours.Filter and package and can be mixed with single-component and to be heating and curing silicon rubber.
The pre-treatment of filler (comprising aluminum oxide, aluminium nitride or aluminium hydroxide), adds 100 parts of (mass parts, as follows) aluminum oxide, aluminium nitride or filling aluminium hydrates in a kettle., stir while add the octamethylcyclotetrasiloxane of 9 parts, stir, then add the hexamethyldisilazane of 15 parts, under N2 air-flow, heat up, keep 100 DEG C and be uniformly mixed 3h, naturally cooling, after normal temperature places 12 hours, reheat to 160 DEG C, dry 5 hours, after cooling, namely obtain the filler after processing.
Embodiment 5
The synthesis of silane coupling agent tackifier: by 100 parts of tetramethyl-tetrahydrochysene cyclotetrasiloxanes, 100 parts of vinyltriethoxysilane mixing, add the platinum complex catalyst of mixture total mass 1 ‰, at 20-DEG C of reaction 24h, then 80 DEG C of reaction 4h are warmed up to, finally be warmed up to 120 DEG C of reactions 3 hours again, after filtering after normal temperature naturally cooling, obtain tackifier.
The pre-treatment of filler (comprising aluminum oxide, aluminium nitride or aluminium hydroxide)
Add 100 parts of (mass parts, as follows) aluminum oxide, aluminium nitride or aluminium hydroxides in a kettle., stir the octamethylcyclotetrasiloxane adding 10 parts, stir, add the hexamethyldisilazane of 20 parts again, under N2 air-flow, heat up, keep 120 DEG C and be uniformly mixed 4h, naturally cooling, after normal temperature places 6 hours, reheats to 180 DEG C, dry 4 hours, after cooling, namely obtain the filler after processing.
The preparation of sizing material:
By vinyl polysiloxane 100 parts, 90 parts, pretreated aluminum oxide, aluminium nitride 60 parts, aluminium hydroxide 45 parts of 20 parts of thermal silicas join in kneader, stir, be warming up to 140 DEG C, vacuumize stirring after 4 hours, take out, three-roller is milled 2 times, obtain the uniform sizing of fillers dispersed.
Get sizing 100 parts to stir in planet still, add the hydrogen based polysiloxane 4 parts obtained according to added sizing quality deal, silane coupling agent tackifier 1 part, 0.01 part of butynol and 0.005 part of hexamethylene alkynol, after stirring, add 0.15 part of platinum catalyst, stir 2-4 hour.Filter and package and can be mixed with single-component and to be heating and curing silicon rubber.
Embodiment 6
The synthesis of silane coupling agent tackifier:
By 100 parts of tetramethyl-tetrahydrochysene cyclotetrasiloxanes, 50 parts of vinyltriethoxysilane mixing, add the platinum catalyst of mixture total mass 2 ‰, at 30 DEG C of reaction 12h, then 100 DEG C of reaction 2h are warmed up to, finally be warmed up to 150 DEG C of reactions 2 hours again, after filtering after normal temperature naturally cooling, obtain tackifier.
The preparation of sizing material:
By vinyl polysiloxane 100 parts, 50 parts, aluminum oxide, aluminium nitride 50 parts, 30 parts, aluminium hydroxide and 10 parts of thermal silicas join in kneader, stir, be warming up to 130 DEG C, vacuumize stirring after 2 hours, take out, three-roller is milled 1 time, obtain the uniform sizing of fillers dispersed.
Get sizing 100 parts to stir in planet still, add the hydrogen based polysiloxane 3 parts obtained according to added sizing quality deal, silane coupling agent tackifier 0.5 part, 0.005 part of butynol and 0.005 part of hexamethylene alkynol, after stirring, add 0.05 part of platinum catalyst, stir 2 hours.Filter and package and can be mixed with single-component and to be heating and curing silicon rubber.
Claims (7)
1. single-component is heating and curing a liquid silastic, measures according to the mass fraction, is made up of following component:
Base glue: vinyl polysiloxane 100 parts,
Heat conductive filler: aluminum oxide 50-100 part and aluminium nitride 50-80 part,
Fire retardant: aluminium hydroxide 30-50 part,
Strengthening agent
:thermal silica 10-20 part;
With calculated according to above base glue, heat conductive filler, fire retardant, strengthening agent total mass part 100 parts
Linking agent: hydrogen based polysiloxane 3-6 part, tackifier: silane coupling agent 0.5-2 part, catalyzer: platinum complex 0.05-0.2 part, stopper: alkynol class stopper 0.01-0.02 part;
Wherein, described aluminum oxide, aluminium nitride heat conductive filler, or aluminium hydroxide fire retardant, be through pretreated aluminum oxide, aluminium nitride heat conductive filler, or aluminium hydroxide fire retardant, and concrete treatment step is as follows:
Add 100 parts of aluminum oxide in a kettle., stir while add the octamethylcyclotetrasiloxane of 5-10 part, stir, add the hexamethyldisilazane of 5-20 part again, be warming up to 80-120 DEG C under nitrogen flowing, carry out being uniformly mixed and keeping 2-4 hour, then naturally cooling, after placing 6-12 hour at 18-25 DEG C, reheat to 150-180 DEG C of dry 4-5 hour, after cooling, namely obtain the aluminum oxide heat conductive filler after processing;
Aluminium nitride heat conductive filler is the same with process aluminum oxide heat conductive filler with the treatment step of aluminium hydroxide fire retardant; The viscosity of wherein said base glue vinyl polysiloxane is 500-50000mpa.s.
2. single-component according to claim 1 is heating and curing liquid silastic, it is characterized in that: described silane coupling agent is vinyltriethoxysilane, vinyltrimethoxy silane or γ-(2,3-epoxy third oxygen) propyl trimethoxy silicane.
3. single-component according to claim 1 is heating and curing liquid silastic, it is characterized in that: described alkynol class stopper is butynol and hexamethylene alkynol.
4. single-component according to claim 3 is heating and curing liquid silastic, it is characterized in that: described alkynol class stopper consumption is 0.005-0.01 part butynol and 0.005-0.01 part hexamethylene alkynol.
5. prepare single-component described in claim 1 to be heating and curing the method for liquid silastic, step is as follows:
Step (1): by base glue vinyl polysiloxane 100 parts, heat conductive filler aluminum oxide 50-100 part and aluminium nitride 50-80 part, fire retardant aluminium hydroxide 30-50 part, strengthening agent thermal silica 10-20 part, be placed in kneader, stir, be warming up to 130-160 DEG C, vacuumize and stir 2-6 hour, put into three-roller after taking-up to mill 1-2 time, obtained sizing;
Step (2): obtained sizing 100 parts is put into planet still and stirs, add the linking agent hydrogen based polysiloxane 3-6 part obtained according to added sizing quality deal again, tackifier silane coupling agent 0.5-2 part, alkynol class stopper 0.01-0.02 part, after stirring, add platinum complex catalyst 0.05-0.2 part, stir 2-4 hour;
Step (3): the material filtering that step (2) is obtained, be packaged to be single-component and be heating and curing silicon rubber.
6. to be heating and curing liquid silastic according to the single-component described in claim 1, to it is characterized in that: described silane coupling agent tackifier, obtain according to the following steps:
By tetramethyl-tetrahydrochysene cyclotetrasiloxane and vinyltriethoxysilane, mix by its quality mol ratio 1:1-2, then the platinum catalyst of its total mass 1-2 ‰ is added, 12-24 hour is reacted at 20-30 DEG C, be warmed up to 80-100 DEG C of reaction 2-4 hour again, finally be warmed up to 120-150 DEG C of reaction 2-4 hour, after naturally cooling, normal temperature filters, and obtains described silane coupling agent tackifier.
7. be heating and curing according to the single-component described in claim 5 preparation method of liquid silastic, it is characterized in that: described silane coupling agent tackifier, obtain according to the following steps:
By tetramethyl-tetrahydrochysene cyclotetrasiloxane and vinyltriethoxysilane, mix by its quality mol ratio 1:1-2, then the platinum catalyst of its total mass 1-2 ‰ is added, 12-24 hour is reacted at 20-30 DEG C, be warmed up to 80-100 DEG C of reaction 2-4 hour again, finally be warmed up to 120-150 DEG C of reaction 2-4 hour, after naturally cooling, normal temperature filters, and obtains described silane coupling agent tackifier.
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Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102725355A (en) * | 2010-01-28 | 2012-10-10 | 道康宁东丽株式会社 | Thermally conductive silicone rubber composition |
| CN103030976A (en) * | 2012-12-27 | 2013-04-10 | 成都拓利化工实业有限公司 | Single-component heat-curing liquid silicone rubber and preparation method thereof |
-
2015
- 2015-11-17 CN CN201510791407.5A patent/CN105331116A/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102725355A (en) * | 2010-01-28 | 2012-10-10 | 道康宁东丽株式会社 | Thermally conductive silicone rubber composition |
| CN103030976A (en) * | 2012-12-27 | 2013-04-10 | 成都拓利化工实业有限公司 | Single-component heat-curing liquid silicone rubber and preparation method thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
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