CN107099148A - A kind of VHD room temperature vulcanization bi-component fireproof silicone rubber and preparation method thereof - Google Patents

A kind of VHD room temperature vulcanization bi-component fireproof silicone rubber and preparation method thereof Download PDF

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CN107099148A
CN107099148A CN201710419036.7A CN201710419036A CN107099148A CN 107099148 A CN107099148 A CN 107099148A CN 201710419036 A CN201710419036 A CN 201710419036A CN 107099148 A CN107099148 A CN 107099148A
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component
parts
powder
room temperature
vhd
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CN107099148B (en
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胡兴胜
康立福
张百舸
魏晓东
李光达
曾宁斌
李天宇
易升贵
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Shanghai Cgn Power Engineering Co Ltd
Jiangsu Five Letter New Materials Polytron Technologies Inc
China Nuclear Power Engineering Co Ltd
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Shanghai Cgn Power Engineering Co Ltd
Jiangsu Five Letter New Materials Polytron Technologies Inc
China Nuclear Power Engineering Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L83/00Compositions 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; Compositions of derivatives of such polymers
    • C08L83/04Polysiloxanes
    • 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
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/08Metals
    • C08K2003/085Copper
    • 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
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/08Metals
    • C08K2003/0856Iron
    • 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
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/08Metals
    • C08K2003/0887Tungsten
    • 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
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2227Oxides; Hydroxides of metals of aluminium
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/08Stabilised against heat, light or radiation or oxydation
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/02Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
    • C08L2205/025Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure

Abstract

It is used for VHD room temperature vulcanization bi-component fireproof silicone rubbers with good nuclear radiation shield function in place such as nuclear power station, hospital, nuclear submarine and preparation method thereof the present invention relates to a kind of, belongs to high molecule sealing materials field.Fireproof silicone rubber in the present invention is made up of component A and B component, calculate by weight, component A includes 100 parts of vinyl polysiloxane, 0.1 5 parts of vinyl platinum catalyst, 0.5 30 parts of silica, 5 120 parts of inorganic combustion inhibitor, 500 1000 parts of surface modification of metals powder;B component includes 100 parts of vinyl polysiloxane, 4 80 parts of polymethyl hydrogen siloxanes, 0.5 30 parts of silica, 5 120 parts of inorganic combustion inhibitor, 500 800 parts of surface modification of metals powder.There is higher tensile strength, elongation at break and radiation-resistant property, it is easier to produce density more than 3.5g/cm after the silicon rubber room temperature vulcanization that the present invention is prepared3Product, while product life is longer.

Description

A kind of VHD room temperature vulcanization bi-component fireproof silicone rubber and preparation method thereof
Technical field
The present invention relates to a kind of good nuclear radiation shield function that has for the place such as nuclear power station, hospital, nuclear submarine VHD room temperature vulcanization bi-component fireproof silicone rubber and preparation method thereof, belongs to high molecule sealing materials field.
Background technology
Nuclear power is clean energy resource, and for the purpose of environmental protection and reduction discharge, China is greatly developing nuclear power station at present Build, nuclear power technology and most material of the construction of nuclear power station need dependence on import before, wherein there is one kind to be built for nuclear power station The encapsulant of perforate on building structure, with functions such as fire prevention, waterproof, nuclear screening.1982.12.27 B&B The United States Patent (USP) of Insulation, Inc. company Application No. 4436868 discloses a kind of bi-component silicon containing lead powder first Rubber, patent produces product trade name Radflex accordingly for Promatec companies, and this company then produces and substituted with iron powder again The like product of lead powder.A large amount of filling lead powder and iron powder impart the higher density of fluid sealant, generally higher than 2.35g/cm3, because Its high density and with good nuclear screening effect, be largely used to nuclear power station.Chinese patent 2010101643560, 2011103942792nd, 201110368015X discloses the similar technique based on the metal dusts such as lead powder, iron powder.
China is building nuclear power station mainly using Generation Ⅲ at present, wherein the China dragon 1 of Chinese independent intellectual property right Number the 3rd nuclear power technology proposes requirements at the higher level to the encapsulant of cable in nuclear island and the through hole of pipeline, it is desirable to which itself and weight are brilliant The nuclear screening effect of stone concrete is identical, that is, density will reach 3.5g/cm3
There are the following problems for prior art:First, present lead powder is prohibitted the use of because of its danger that there is infringement people's health; Second, other metal dusts such as iron powder are typically not less than 45 micro- because hardness is high and activity is extremely difficult to thinner particle diameter by force Meter, largely particle diameter is powder filled greatly can significantly reduce its physical and mechanical properties in high material, it is impossible to meet to use well and want Ask;3rd, to reach 3.5g/cm3Density, it is necessary to largely fill powder, cause each group viscosity high, poor fluidity is difficult to apply Work, the product tensile strength after solidification is very low, it is impossible to meet application requirement.
The content of the invention
In view of the above-mentioned problems, the present invention, which provides a kind of safety, density, reaches 3.5g/cm3, each component good fluidity, construction Easy, solidification after-drawing intensity exceedes 3MPa VHD room temperature vulcanization bi-component fireproof silicone rubber.
Technical scheme is as follows.
A kind of VHD room temperature vulcanization two-component silicone rubber, is made up of component A and B component.Calculate by weight, A Component includes 100 parts of vinyl polysiloxane, 0.1-5 parts of vinyl platinum catalyst, 0.5-30 parts of silica, 5- 120 parts of inorganic combustion inhibitor, 500-1000 parts of surface modification of metals powder.Calculated also according to parts by weight, B component is included 100 parts of vinyl polysiloxane, 4-80 parts of polymethyl hydrogen siloxanes, 0.5-30 parts of silica, 5-120 parts of inorganic resistance Fire agent, 500-800 parts of surface modification of metals powder.A, B component by weight 1:1 hybrid reaction, after solidification, the density of resulting product More than or equal to 3.5g/cm3
The vinyl polysiloxane is end-vinyl dimethyl silicone polymer, the poly- methyl ethylene silica of end-vinyl One or more of combinations in the double phenyl polysiloxanes of alkane, many vinyl.
Described silica is one or two kinds of combinations of aerosil or precipitated silica.
Described inorganic combustion inhibitor is one or more of combinations in aluminium hydroxide, magnesium hydroxide, Firebrake ZB.
Described surface modification of metals powder, refers to the metal powder being surface-treated with VTES, gold Category powder is one or more of combinations in iron powder, copper powder, tungsten powder.The average grain diameter of described metal powder is less than 50 microns.Gold The particle diameter of category powder directly affects the physical property of product, such as intensity, radiation-resistant property.1 ~ 25 micron of optimized particle size scope.
In the present invention, the preparation method of VHD room temperature vulcanization two-component silicone rubber includes following 3 step.
1st, surface modification is carried out to metal powder:(1)VTES is dissolved in the mixed liquor shape of water and ethanol Into solution, the mass ratio of its reclaimed water and ethanol is 100:1~100:50, the quality of VTES in the solution Concentration is 0.2% ~ 10%;(2)The solution that the first step is configured is with metal powder in spraying high-speed mixer and mixing, every 100 parts of metal powders End, 0.2 ~ 10 part of the solution configured using the first step, speed of agitator is not less than 100 revs/min, 3 ~ 10 minutes time;(3)By The metal that two steps are mixed point is extracted, and is dried 1 hour in 105 DEG C of high temperature ovens.
2nd, component A is prepared:(1)Vinyl polysiloxane and platinum catalyst are put into the scuffing of cylinder bore of high speed dispersor successively; (2)Open high speed dispersor, the linear velocity of dispersion impeller sequentially adds silica in the range of 2 ~ 5m/s, inorganic combustion inhibitor and Surface modification of metals powder;(3)The speed of agitator of high speed dispersor is improved, allows the linear velocity of dispersion impeller to reach more than 10m/s, is continued It is scattered more than 60 minutes;(4)By in the one of container for preparing the component A loading bi-component glue bottles completed.
3rd, component B is prepared:(1)Vinyl polysiloxane and polymethyl hydrogen siloxane are put into the drawing of high speed dispersor successively In cylinder;(2)High speed dispersor is opened, the linear velocity of dispersion impeller sequentially adds silica in the range of 2 ~ 5m/s, inorganic fire-retarded Agent and surface modification of metals powder;(3)The speed of agitator of high speed dispersor is improved, allows the linear velocity of dispersion impeller to reach more than 10m/s, Continue scattered more than 60 minutes;(4)By in the other in which container for preparing the component B loading bi-component glue bottles completed.
The A for preparing according to the method described above, B component not Zhuan Yu bi-component glue bottle two connected independent hydrostatic columns In, hydrostatic column afterbody has piston seal, and glue rifle promotes two pistons extrusion A, B components simultaneously when using, by mounted in The static mixer mixing A of outlet, B component.In platinum after vinyl polysiloxane and polymethyl hydrogen siloxane mixing in formula Cross-linking reaction can be produced under the catalysis of catalyst, silicon rubber is generated.So when designing two-part formulations, by platinum catalyst and poly- Methyl hydrogen siloxane is separately packed.
The present invention fills two-component silicone rubber using the modified metal dust in surface, to obtain the density of superelevation.It is real Testing result proves, non-modified metal dust is difficult to realize largely fills in two-component silicone rubber.And add surface modification The beneficial effect that metal dust is brought has:1st, in the case of identical addition, A, the viscosity of B component are significantly reduced, it is ensured that had Preferable mobility;2nd, in the case of identical addition, the product after room temperature vulcanization has higher tensile strength, extension at break Rate and radiation-resistant property;3rd, it is easier to produce density more than 3.5g/cm3Product;4th, prevent the metal powder in product normal Aoxidized when using, improve product life.
Embodiment
The present invention is described further with reference to instantiation.
Embodiment 1.
1st, surface modification is carried out to metal powder:(1)VTES is dissolved in the mixed liquor shape of water and ethanol Into solution, the mass ratio of its reclaimed water and ethanol is 100:15, the mass concentration of VTES in the solution is 5%;(2)The iron powder of 10 microns of solution that the first step is configured and average grain diameter is in spraying high-speed mixer and mixing, every 100 parts of iron powders, 8 parts of the solution configured using the first step, 100 revs/min of speed of agitator, 5 minutes time;(3)The iron powder that second step is mixed Divide and extract, dried 1 hour in 105 DEG C of high temperature ovens.
2nd, component A is prepared:(1)Successively by 100 parts of contents of ethylene be 0.3% end-vinyl dimethyl silicone polymer and 2 Part vinyl platinum catalyst is put into the scuffing of cylinder bore of high speed dispersor;(2)Open high speed dispersor, the linear velocity of dispersion impeller 2 ~ In the range of 5m/s, 10 parts of aerosils are sequentially added, 120 parts of aluminium hydroxides and 750 parts of surfaces are modified iron powder;(3)Improve The speed of agitator of high speed dispersor, allows the linear velocity of dispersion impeller to reach more than 10m/s, continues scattered more than 60 minutes;(4)Will system The standby component A completed loads in one of container of bi-component glue bottle.
3rd, component B is prepared:(1)Successively by 100 parts of contents of ethylene for 0.3% end-vinyl dimethyl silicone polymer and 30 parts of hydrogen contents are put into the scuffing of cylinder bore of high speed dispersor for 0.35% polymethyl hydrogen siloxane;(2)High speed dispersor is opened, point The linear velocity of disk is dissipated in the range of 2 ~ 5m/s, sequentially adds 10 parts of aerosils, 120 parts of aluminium hydroxide and 700 parts Surface is modified iron powder;(3)The speed of agitator of high speed dispersor is improved, allows the linear velocity of dispersion impeller to reach more than 10m/s, continues to divide Dissipate more than 60 minutes;(4)By in the other in which container for preparing the component B loading bi-component glue bottles completed.
A, B component are not fitted into bi-component glue bottle, extrusion is placed in mould, react sample preparation, conserved 7 days after after its solidification Measure.The size of sample 1 is 50mm × 50mm × 50mm, surveys its density for 3.56g/cm3.The size of sample 2 is 13mm × 6mm × 2mm dumbbell shape samples, survey tensile strength is 4.50MP.
Embodiment 2.
1st, surface modification is carried out to metal powder:(1)VTES is dissolved in the mixed liquor shape of water and ethanol Into solution, the mass ratio of its reclaimed water and ethanol is 100:20, the mass concentration of VTES in the solution is 5%;(2)The copper powder of 25 microns of solution that the first step is configured and average grain diameter is in spraying high-speed mixer and mixing, every 100 parts of copper powders, 5 parts of the solution configured using the first step, 100 revs/min of speed of agitator, 5 minutes time;(3)The copper powder that second step is mixed Divide and extract, dried 1 hour in 105 DEG C of high temperature ovens.
2nd, component A is prepared:(1)Successively by 100 parts of contents of ethylene be 0.3% end-vinyl dimethyl silicone polymer and 2 Part vinyl platinum catalyst is put into the scuffing of cylinder bore of high speed dispersor;(2)Open high speed dispersor, the linear velocity of dispersion impeller 2 ~ In the range of 5m/s, 10 parts of aerosils are sequentially added, 100 parts of aluminium hydroxides and 650 parts of surfaces are modified copper powder;(3)Improve The speed of agitator of high speed dispersor, allows the linear velocity of dispersion impeller to reach more than 10m/s, continues scattered more than 60 minutes;(4)Will system The standby component A completed loads in one of container of bi-component glue bottle.
3rd, component B is prepared:(1)Successively by 100 parts of contents of ethylene for 0.3% end-vinyl dimethyl silicone polymer and 25 parts of hydrogen contents are put into the scuffing of cylinder bore of high speed dispersor for 0.35% polymethyl hydrogen siloxane;(2)High speed dispersor is opened, point The linear velocity of disk is dissipated in the range of 2 ~ 5m/s, sequentially adds 10 parts of aerosils, 100 parts of aluminium hydroxide and 680 parts of tables Face is modified copper powder;(3)The speed of agitator of high speed dispersor is improved, allows the linear velocity of dispersion impeller to reach more than 10m/s, continues scattered More than 60 minutes;(4)By in the other in which container for preparing the component B loading bi-component glue bottles completed.
A, B component are not fitted into bi-component glue bottle, extrusion is placed in mould, react sample preparation, conserved 7 days after after its solidification Measure.The size of sample 1 is 50mm × 50mm × 50mm, surveys its density for 3.64g/cm3.The size of sample 2 is 13mm × 6mm × 2mm dumbbell shape samples, survey tensile strength is 3.80MP.
Embodiment 3.
1st, surface modification is carried out to metal powder:(1)VTES is dissolved in the mixed liquor shape of water and ethanol Into solution, the mass ratio of its reclaimed water and ethanol is 100:30, the mass concentration of VTES in the solution is 8%;(2)The tungsten powder of 50 microns of solution that the first step is configured and average grain diameter is in spraying high-speed mixer and mixing, every 100 parts of tungsten powders, 2 parts of the solution configured using the first step, 100 revs/min of speed of agitator, 10 minutes time;(3)The tungsten powder that second step is mixed Divide and extract, dried 1 hour in 105 DEG C of high temperature ovens.
2nd, component A is prepared:(1)Successively by 100 parts of contents of ethylene be 0.3% end-vinyl dimethyl silicone polymer and 2 Part vinyl platinum catalyst is put into the scuffing of cylinder bore of high speed dispersor;(2)Open high speed dispersor, the linear velocity of dispersion impeller 2 ~ In the range of 5m/s, 15 parts of aerosils are sequentially added, 100 parts of aluminium hydroxides and 450 parts of surface are modified tungsten powder;(3)Carry The speed of agitator of high high speed dispersor, allows the linear velocity of dispersion impeller to reach more than 10m/s, continues scattered more than 60 minutes;(4)Will The component A completed is prepared to load in one of container of bi-component glue bottle.
3rd, component B is prepared:(1)Successively by 100 parts of contents of ethylene for 0.3% end-vinyl dimethyl silicone polymer and 25 parts of hydrogen contents are put into the scuffing of cylinder bore of high speed dispersor for 0.35% polymethyl hydrogen siloxane;(2)High speed dispersor is opened, point The linear velocity of disk is dissipated in the range of 2 ~ 5m/s, sequentially adds 15 parts of aerosils, 100 parts of aluminium hydroxide and 470 parts of tables Face is modified tungsten powder;(3)The speed of agitator of high speed dispersor is improved, allows the linear velocity of dispersion impeller to reach more than 10m/s, continues scattered More than 60 minutes;(4)By in the other in which container for preparing the component B loading bi-component glue bottles completed.
A, B component are not fitted into bi-component glue bottle, extrusion is placed in mould, react sample preparation, conserved 7 days after after its solidification Measure.The size of sample 1 is 50mm × 50mm × 50mm, surveys its density for 3.59g/cm3.The size of sample 2 is 13mm × 6mm × 2mm dumbbell shape samples, survey tensile strength is 3.20MP.
Embodiment 4.
1st, surface modification is carried out to metal powder:(1)VTES is dissolved in the mixed liquor shape of water and ethanol Into solution, the mass ratio of its reclaimed water and ethanol is 100:10, the mass concentration of VTES in the solution is 5%;(2)The tungsten powder of 50 microns of solution that the first step is configured and average grain diameter is in spraying high-speed mixer and mixing, every 100 parts of tungsten powders, 2 parts of the solution configured using the first step, 100 revs/min of speed of agitator, 10 minutes time;(3)The tungsten powder that second step is mixed Divide and extract, dried 1 hour in 105 DEG C of high temperature ovens.
2nd, component A is prepared:(1)Successively by 100 parts of contents of ethylene for 0.3% end-vinyl dimethyl silicone polymer and 0.5 part of vinyl platinum catalyst is put into the scuffing of cylinder bore of high speed dispersor;(2)High speed dispersor is opened, the linear velocity of dispersion impeller is 2 In the range of ~ 5m/s, 5 parts of aerosils are sequentially added, 20 parts of aluminium hydroxides and 450 parts of surfaces are modified tungsten powder;(3)Improve high The speed of agitator of fast dispersion machine, allows the linear velocity of dispersion impeller to reach more than 10m/s, continues scattered more than 60 minutes;(4)It will prepare The component A of completion loads in one of container of bi-component glue bottle.
3rd, component B is prepared:(1)Successively by 100 parts of contents of ethylene for 0.3% end-vinyl dimethyl silicone polymer and 10 parts of hydrogen contents are put into the scuffing of cylinder bore of high speed dispersor for 0.35% polymethyl hydrogen siloxane;(2)High speed dispersor is opened, point The linear velocity of disk is dissipated in the range of 2 ~ 5m/s, sequentially adds 30 parts of aerosils, 120 parts of aluminium hydroxide and 470 parts of tables Face is modified tungsten powder;(3)The speed of agitator of high speed dispersor is improved, allows the linear velocity of dispersion impeller to reach more than 10m/s, continues scattered More than 60 minutes;(4)By in the other in which container for preparing the component B loading bi-component glue bottles completed.
Embodiment 5.
1st, surface modification is carried out to metal powder:(1)VTES is dissolved in the mixed liquor shape of water and ethanol Into solution, the mass ratio of its reclaimed water and ethanol is 100:10, the mass concentration of VTES in the solution is 5%;(2)The iron powder of 10 microns of solution that the first step is configured and average grain diameter is in spraying high-speed mixer and mixing, every 100 parts of iron powders, 5 parts of the solution configured using the first step, 100 revs/min of speed of agitator, 10 minutes time;(3)The iron powder that second step is mixed Divide and extract, dried 1 hour in 105 DEG C of high temperature ovens.
2nd, component A is prepared:(1)Successively by 100 parts of contents of ethylene be 0.3% end-vinyl dimethyl silicone polymer and 5 Part vinyl platinum catalyst is put into the scuffing of cylinder bore of high speed dispersor;(2)Open high speed dispersor, the linear velocity of dispersion impeller 2 ~ In the range of 5m/s, 10 parts of precipitated silicas are sequentially added, 100 parts of magnesium hydroxides and 750 parts of surfaces are modified iron powder;(3)Carry The speed of agitator of high high speed dispersor, allows the linear velocity of dispersion impeller to reach more than 10m/s, continues scattered more than 60 minutes;(4)Will The component A completed is prepared to load in one of container of bi-component glue bottle.
3rd, component B is prepared:(1)Successively by 100 parts of contents of ethylene for 0.3% end-vinyl dimethyl silicone polymer and 70 parts of hydrogen contents are put into the scuffing of cylinder bore of high speed dispersor for 0.35% polymethyl hydrogen siloxane;(2)High speed dispersor is opened, point The linear velocity of disk is dissipated in the range of 2 ~ 5m/s, sequentially adds 10 parts of precipitated silicas, 120 parts of magnesium hydroxide and 700 parts Surface be modified iron powder;(3)The speed of agitator of high speed dispersor is improved, allows the linear velocity of dispersion impeller to reach more than 10m/s, is continued It is scattered more than 60 minutes;(4)By in the other in which container for preparing the component B loading bi-component glue bottles completed.
Embodiment 6.
1st, surface modification is carried out to metal powder:(1)VTES is dissolved in the mixed liquor shape of water and ethanol Into solution, the mass ratio of its reclaimed water and ethanol is 100:30, the mass concentration of VTES in the solution is 5%;(2)The iron powder of 10 microns of solution that the first step is configured and average grain diameter is in spraying high-speed mixer and mixing, every 100 parts of iron powders, 5 parts of the solution configured using the first step, 100 revs/min of speed of agitator, 10 minutes time;(3)The iron powder that second step is mixed Divide and extract, dried 1 hour in 105 DEG C of high temperature ovens.
2nd, component A is prepared:(1)Successively by 100 parts of contents of ethylene be 0.3% end-vinyl dimethyl silicone polymer and 1 Part vinyl platinum catalyst is put into the scuffing of cylinder bore of high speed dispersor;(2)Open high speed dispersor, the linear velocity of dispersion impeller 2 ~ In the range of 5m/s, 10 parts of precipitated silicas are sequentially added, 120 parts of aluminium hydroxides and 750 parts of surfaces are modified iron powder;(3)Carry The speed of agitator of high high speed dispersor, allows the linear velocity of dispersion impeller to reach more than 10m/s, continues scattered more than 60 minutes;(4)Will The component A completed is prepared to load in one of container of bi-component glue bottle.
3rd, component B is prepared:(1)Successively by 100 parts of contents of ethylene for 0.3% end-vinyl dimethyl silicone polymer and 50 parts of hydrogen contents are put into the scuffing of cylinder bore of high speed dispersor for 0.35% polymethyl hydrogen siloxane;(2)High speed dispersor is opened, point The linear velocity of disk is dissipated in the range of 2 ~ 5m/s, sequentially adds 10 parts of precipitated silicas, 20 parts of aluminium hydroxide and 700 parts Surface is modified iron powder;(3)The speed of agitator of high speed dispersor is improved, allows the linear velocity of dispersion impeller to reach more than 10m/s, continues to divide Dissipate more than 60 minutes;(4)By in the other in which container for preparing the component B loading bi-component glue bottles completed.

Claims (9)

1. a kind of VHD room temperature vulcanization bi-component fireproof silicone rubber, it is characterised in that:It is made up of component A and B component, presses Parts by weight calculate, component A comprising 100 parts vinyl polysiloxane, 0.1-5 parts of vinyl platinum catalyst, 0.5-30 parts Silica, 5-120 parts of inorganic combustion inhibitor, 500-1000 parts of surface modification of metals powder, B component includes 100 parts of second Alkenyl polysiloxanes, 4-80 part polymethyl hydrogen siloxane, 0.5-30 parts of silica, 5-120 parts of inorganic combustion inhibitor, 500- 800 parts of surface modification of metals powder.
2. a kind of VHD room temperature vulcanization bi-component fireproof silicone rubber as claimed in claim 1, it is characterised in that:Described Vinyl polysiloxane is end-vinyl dimethyl silicone polymer, end-vinyl Polymethyl methacrylate, many vinyl pair One or more of combinations in phenyl polysiloxane.
3. a kind of VHD room temperature vulcanization bi-component fireproof silicone rubber as claimed in claim 1, it is characterised in that:Described Silica is one or both of aerosil or precipitated silica.
4. a kind of VHD room temperature vulcanization bi-component fireproof silicone rubber as claimed in claim 1, it is characterised in that:Described Inorganic combustion inhibitor is one or more of combinations in aluminium hydroxide, magnesium hydroxide, Firebrake ZB.
5. a kind of VHD room temperature vulcanization bi-component fireproof silicone rubber as claimed in claim 1, it is characterised in that:Described Surface modification of metals powder, refers to the metal powder being surface-treated with VTES, and metal powder is iron powder, copper One or more of combinations in powder, tungsten powder.
6. a kind of VHD room temperature vulcanization bi-component fireproof silicone rubber as claimed in claim 5, it is characterised in that:Described Surface modification of metals powder, average grain diameter is less than 50 microns.
7. a kind of VHD room temperature vulcanization bi-component fireproof silicone rubber as claimed in claim 6, it is characterised in that:Described Surface modification of metals powder, average grain diameter preferably is 1-25 microns.
8. a kind of application method of VHD room temperature vulcanization bi-component fireproof silicone rubber, it is characterised in that:By A, B for preparing Component is respectively in two connected independent hydrostatic columns loaded on bi-component glue bottle, and hydrostatic column afterbody has piston seal, Glue rifle promotes two piston extrusion A, B components simultaneously when using, and passes through the static mixer mixing A mounted in outlet, B component.
9. a kind of preparation method of VHD room temperature vulcanization bi-component fireproof silicone rubber, it is characterised in that comprise the following steps:
1)Surface modification is carried out to metal powder:(1)The mixed liquor that VTES is dissolved in water and ethanol is formed molten The mass ratio of liquid, its reclaimed water and ethanol is 100:1~100:50, the mass concentration of VTES in the solution For 0.2% ~ 10%;(2)The solution that the first step is configured is with metal powder in spraying high-speed mixer and mixing, and every 100 parts of metal dusts make 0.2 ~ 10 part of the solution configured with the first step, speed of agitator is not less than 100 revs/min, 3 ~ 10 minutes time;(3)By second step The metal mixed point is extracted, and is dried 1 hour in 105 DEG C of high temperature ovens;
2nd, component A is prepared:(1)Vinyl polysiloxane and platinum catalyst are put into the scuffing of cylinder bore of high speed dispersor successively;(2)Open High speed dispersor is opened, the linear velocity of dispersion impeller sequentially adds silica in the range of 2 ~ 5m/s, and inorganic combustion inhibitor and surface change Property metal powder;(3)The speed of agitator of high speed dispersor is improved, allows the linear velocity of dispersion impeller to reach more than 10m/s, continues scattered 60 More than minute;(4)By in the one of container for preparing the component A loading bi-component glue bottles completed;
3rd, component B is prepared:(1)Vinyl polysiloxane and polymethyl hydrogen siloxane are put into the scuffing of cylinder bore of high speed dispersor successively In;(2)High speed dispersor is opened, the linear velocity of dispersion impeller sequentially adds silica, inorganic combustion inhibitor in the range of 2 ~ 5m/s With surface modification of metals powder;(3)The speed of agitator of high speed dispersor is improved, allows the linear velocity of dispersion impeller to reach more than 10m/s, after It is continuous scattered more than 60 minutes;(4)By in the other in which container for preparing the component B loading bi-component glue bottles completed.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109096769A (en) * 2018-05-31 2018-12-28 镇江高美新材料有限公司 A kind of high-strength anti-flaming silicone rubber compound
CN112201564A (en) * 2020-09-30 2021-01-08 德清县蓝鸟照明电器有限公司 High-strength explosion-proof film-coated infrared lamp bulb and production process thereof
CN116814077A (en) * 2023-08-25 2023-09-29 四川犀迈湾科技有限公司 Bi-component heat-conducting gel and preparation method and application thereof

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101624471A (en) * 2009-03-06 2010-01-13 上海锐朗光电材料有限公司 Heat curing in-situ forming high-conductivity silicon rubber composition and application thereof
CN104342081A (en) * 2014-09-17 2015-02-11 烟台德邦科技有限公司 Double-component high-temperature vulcanized conductive glue and preparation method thereof
CN104725870A (en) * 2014-12-17 2015-06-24 苏州锦腾电子科技有限公司 High-conductivity silicon rubber and preparation method thereof
CN105131610A (en) * 2015-08-27 2015-12-09 江苏海龙核科技股份有限公司 Organic-inorganic composite biological shielding material for nuclear power and preparing method thereof
CN105199623A (en) * 2015-10-30 2015-12-30 深圳德邦界面材料有限公司 Double-component addition type anti-sedimentation conductive silicone rubber and preparation method thereof
CN105238059A (en) * 2015-11-06 2016-01-13 深圳德邦界面材料有限公司 Silicon-based wave absorption glue easy to mold, and preparation method thereof
CN106010426A (en) * 2016-06-25 2016-10-12 烟台德邦科技有限公司 Sedimentation preventing and wave absorbing silicon-based glue with high adhesion
CN106590522A (en) * 2016-12-30 2017-04-26 江苏晶河电子科技有限公司 High temperature and corrosion resistant HTV conductive glue and preparation method thereof

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101624471A (en) * 2009-03-06 2010-01-13 上海锐朗光电材料有限公司 Heat curing in-situ forming high-conductivity silicon rubber composition and application thereof
CN104342081A (en) * 2014-09-17 2015-02-11 烟台德邦科技有限公司 Double-component high-temperature vulcanized conductive glue and preparation method thereof
CN104725870A (en) * 2014-12-17 2015-06-24 苏州锦腾电子科技有限公司 High-conductivity silicon rubber and preparation method thereof
CN105131610A (en) * 2015-08-27 2015-12-09 江苏海龙核科技股份有限公司 Organic-inorganic composite biological shielding material for nuclear power and preparing method thereof
CN105199623A (en) * 2015-10-30 2015-12-30 深圳德邦界面材料有限公司 Double-component addition type anti-sedimentation conductive silicone rubber and preparation method thereof
CN105238059A (en) * 2015-11-06 2016-01-13 深圳德邦界面材料有限公司 Silicon-based wave absorption glue easy to mold, and preparation method thereof
CN106010426A (en) * 2016-06-25 2016-10-12 烟台德邦科技有限公司 Sedimentation preventing and wave absorbing silicon-based glue with high adhesion
CN106590522A (en) * 2016-12-30 2017-04-26 江苏晶河电子科技有限公司 High temperature and corrosion resistant HTV conductive glue and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
张书华,等: "《高性能电缆材料及其应用技术》", 30 November 2015, 上海交通大学出版社 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109096769A (en) * 2018-05-31 2018-12-28 镇江高美新材料有限公司 A kind of high-strength anti-flaming silicone rubber compound
CN112201564A (en) * 2020-09-30 2021-01-08 德清县蓝鸟照明电器有限公司 High-strength explosion-proof film-coated infrared lamp bulb and production process thereof
CN116814077A (en) * 2023-08-25 2023-09-29 四川犀迈湾科技有限公司 Bi-component heat-conducting gel and preparation method and application thereof
CN116814077B (en) * 2023-08-25 2023-11-17 四川犀迈湾科技有限公司 Bi-component heat-conducting gel and preparation method and application thereof

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