CN109054302A - Thermal interfacial material and preparation method thereof - Google Patents

Thermal interfacial material and preparation method thereof Download PDF

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Publication number
CN109054302A
CN109054302A CN201810871021.9A CN201810871021A CN109054302A CN 109054302 A CN109054302 A CN 109054302A CN 201810871021 A CN201810871021 A CN 201810871021A CN 109054302 A CN109054302 A CN 109054302A
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Prior art keywords
interfacial material
thermal interfacial
coupling agent
boron nitride
thermal
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CN201810871021.9A
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Chinese (zh)
Inventor
孙蓉
任琳琳
曾小亮
许建斌
汪正平
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Shenzhen Institute of Advanced Technology of CAS
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Shenzhen Institute of Advanced Technology of CAS
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Priority to CN201810871021.9A priority Critical patent/CN109054302A/en
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    • 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
    • C08K7/00Use of ingredients characterised by shape
    • C08K7/16Solid spheres
    • C08K7/18Solid spheres inorganic
    • 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
    • C08K5/00Use of organic ingredients
    • C08K5/54Silicon-containing compounds
    • C08K5/541Silicon-containing compounds containing oxygen
    • C08K5/5435Silicon-containing compounds containing oxygen containing oxygen in a ring
    • 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
    • C08K5/00Use of organic ingredients
    • C08K5/54Silicon-containing compounds
    • C08K5/544Silicon-containing compounds containing nitrogen
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K5/00Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
    • C09K5/08Materials not undergoing a change of physical state when used
    • C09K5/14Solid materials, e.g. powdery or granular

Abstract

The present invention relates to a kind of thermal interfacial materials and preparation method thereof.A kind of thermal interfacial material includes spherical boron nitride 30~70%, thermosetting resin 20-50%, curing agent 5-10%, coupling agent 1-5%, diluent 1-10% as mass fraction.The preparation method is that spherical boron nitride, thermosetting resin, curing agent, defoaming agent, coupling agent and diluent are uniformly mixed by a certain percentage.Thermal interfacial material is obtained using curing oven.The present invention replaces platelet boron nitride using spherical boron nitride, loading of the boron nitride in thermosetting resin can be improved, to improve the coefficient of thermal conductivity of thermal interfacial material;Meanwhile spherical boron nitride can reduce the viscosity of composite material, improve the operating performance of thermal interfacial material.This method is simple and easy, and cost of material is cheap, and the thermal interfacial material thermal coefficient of preparation is higher, can be widely applied to high-density electronic device field of radiating.

Description

Thermal interfacial material and preparation method thereof
Technical field
The invention belongs to electronic package material field, it is related to a kind of thermal interfacial material and preparation method thereof.
Background technique
As the integrated level of electronic device to micromation, miniaturization development and electronic chip is higher and higher, electronics The working efficiency and reliability of device are increasingly dependent on the solution of heat dissipation problem, therefore the heat dissipation of Electronic Packaging becomes more to weigh It wants.Thermal interfacial material is generally used for integrated circuit (chip) or microprocessor and cooling fin or equal backing and equal backing and dissipates Solid interface between backing.The height of thermal interfacial material thermal coefficient directly affects the heat dissipation performance of chip.Therefore, exploitation heat Boundary material is particularly important.
The polymer matrix thermal interfacial material of Inorganic Fillers Filled has high heat conductance by filling into polymeric matrix The mode of ceramic particle realizes the raising of heat transfer property.Processing temperature of the polymer thermal interface materials due to maintaining polymer It is low, flexible, easy to operate, it is the most commonly used material of current thermal interfacial material in conjunction with the characteristics of inorganic filler high thermal conductivity coefficient.By Have the characteristics that thermal coefficient height, good insulating, breakdown voltage resistant strong in ceramic particle, is presently the most common and inorganic fills out Material, common ceramic packing includes aluminium oxide, aluminium nitride, boron nitride, silicon nitride, silicon carbide.Boron nitride has good electricity absolutely Edge has extraordinary inoxidizability and corrosion resistance.Common boron nitride has unformed and six side of sum of cubes etc. a variety of Crystal form.Hexagonal boron nitride is most stable of crystal form, there is the layer structure similar to graphite, has the title of white graphite, by extensive Research and application.Due to the superior function of boron nitride itself, have in the heat filling as heat conductive insulating polymer composites Good prospect.But boron nitride is typically all laminated structure, and density is stronger.When it is with mixed with polymers, cause to polymerize Object viscosity steeply rises, and causes nitridation Boron addition limited, and the polymer thermal interface materials thermal coefficient of preparation is lower, and due to Viscosity is larger, and operability is poor.
Summary of the invention
The object of the present invention is to provide a kind of thermal interfacial materials and preparation method thereof, are led with the thermal interfacial material for solving current The imperfect technical problem of hot property.
In order to achieve the above-mentioned object of the invention, an aspect of of the present present invention provides a kind of thermal interfacial material.The hot interface material Material is by including that the component of following mass percent is formed:
Preferably, the diameter of the spherical boron nitride is 5 μm~200 μm.
Preferably, the thermosetting resin is liquid epoxies or organic siliconresin.
Specifically, the liquid epoxies is bisphenol A-type liquid epoxy resin, bisphenol F-type epoxy resin, alicyclic ring One of race's liquid-state epoxy resin is a variety of.
Specifically, the organic siliconresin is poly- methyl silicon resin, poly- ethyl silicone resin, polyphenylene silicone resin, polyphenylene One of methyl silicon resin is a variety of.
Preferably, the curing agent is methyl hexahydrophthalic anhydride, tetraethylenepentamine, m-phenylene diamine (MPD), 2- ethyl -4- methyl miaow Azoles, N, one of N- dimethyl benzylamine and three-(dimethylamino methyl) phenol or a variety of.
Preferably, the coupling agent is silane coupling agent, titanate coupling agent, aluminate coupling agent, bimetallic coupling agent One of or it is a variety of.
Specifically, the silane coupling agent is one of KH550 coupling agent, KH560 coupling agent or KH570 coupling agent Or it is a variety of.
Preferably, the diluent is glycidol ether, preferably n-butyl glycidyl ether, diglycidyl ether, Isosorbide-5-Nitrae- One of butanediol diglycidyl ether, polyglycidyl ether, trihydroxy methyl propane glycidol ether are a variety of.
Preferably, the thermal coefficient of the thermal interfacial material is 0.5-6W/mK.
Another aspect of the present invention provides a kind of method of preparing heat interfacial material.The method of preparing heat interfacial material includes Following steps:
The spherical boron nitride, thermosetting resin, curing agent, defoaming agent, coupling agent and diluent are subjected to mixed processing, Form mixture;
The mixture processing that be heating and curing is obtained into thermal interfacial material.
Preferably, described be heating and curing as temperature is 60-200 DEG C, and the time that is heating and curing is 0.5-6h.
It preferably, include ball-milling treatment during the mixed processing, the parameter of the ball-milling technology are as follows: ball milling speed 200~500rpm;Ball-milling Time is 0.5~2h;
Thermal interfacial material of the present invention replaces platelet boron nitride using spherical boron nitride, and spherical boron nitride can reduce composite wood The viscosity of material improves the technical effect of loading of the boron nitride in thermosetting resin to reach;The heating conduction of boron nitride simultaneously Much higher than the heating conduction of other raw materials, therefore, the excellent thermal conductivity of the thermal interfacial material, and viscosity is small before solidification, Strong operability.
Contained component is carried out mixed processing by method of preparing heat interfacial material of the present invention, therefore the preparation method can The thermal interfacial material performance that preparation is effectively ensured is stablized, and assigns the thermal interfacial material excellent heating conduction, and before curing With smaller viscosity characteristics.In addition described preparation method is simple, and cost of material is cheap, and the material property being prepared is excellent It is different.
Detailed description of the invention
Fig. 1 is thermal interfacial material of embodiment of the present invention structural schematic diagram;10 be polymer;20 be spherical boron nitride;
Fig. 2 is spherical boron nitride of embodiment of the present invention scanning electron microscope diagram.
Specific embodiment
In order to which technical problems, technical solutions and advantageous effects to be solved by the present invention are more clearly understood, below in conjunction with Embodiment, the present invention will be described in further detail.It should be appreciated that specific embodiment described herein is only used to explain The present invention is not intended to limit the present invention.
On the one hand, the embodiment of the invention provides a kind of thermal interfacial materials.The thermal interfacial material uses spherical boron nitride The heating conduction that material is improved instead of platelet boron nitride is 0.5- by the thermal coefficient that test obtains the thermal interfacial material 6W/mK.Below by way of specific embodiments and the drawings, the invention will be further described.
The thermal interfacial material is by including that the component of following mass percent is formed:
Specifically, the diameter of the spherical boron nitride is 5 μm~200 μm.Compared to platelet boron nitride, phase homogenous quantities it is spherical The volume of boron nitride is smaller, and boron nitride is much larger than other raw materials to the contribution of viscosity in molten system to be processed, because Can not liquefy for boron nitride is existed in the form of solid granule.Compared to sheet when using spherical boron nitride as raw material Boron nitride, one side volume is smaller, and the probability for encountering machining object is smaller, and the viscosity resistance of generation is smaller;On the other hand spherical nitridation It is rolling friction that boron, which encounters machining object, but also the viscosity resistance generated is smaller;On the one hand, spherical boron nitride is more than volume It is small, it is easier to disperse, it is excessive to avoid the local viscosity resistance reunited and generated.Therefore the property showed is exactly with nitridation Boron mass ratio rises in system, and spherical boron nitride system medium viscosity rises slower.Before reaching processable upper viscosity limit Fillable spherical boron nitride is more.And the heating conduction of boron nitride is much higher than other components in material, therefore with boron nitride The promotion material overall thermal conductivity of mass ratio can be promoted also.Boron nitride also has good electrical insulating property, corrosion resistance simultaneously And inoxidizability, it is all property required for the thermal interfacial material.
The thermosetting resin is liquid epoxies or organic siliconresin.The shared property of both resins is, heat-resisting Insulation performance might as well while performance is good.For the thermal interfacial material, this two properties are all important beneficial effect.
In one embodiment, the liquid epoxies is bisphenol A-type liquid epoxy resin, bisphenol-f type liquid ring One of oxygen resin, alicyclic liquid-state epoxy resin are a variety of.
In another embodiment, the organic siliconresin is poly- methyl silicon resin, poly- ethyl silicone resin, polyphenylene silicon One of resin, polyphenyl methyl silicone resin are a variety of.
The curing agent is methyl hexahydrophthalic anhydride, tetraethylenepentamine, m-phenylene diamine (MPD), 2-ethyl-4-methylimidazole, N, N- bis- One of methylbenzylamine and three-(dimethylamino methyl) phenol are a variety of.Selected curing agent boiling point all with higher, It can guarantee that curing agent will not excessively volatilize to influence solidification effect in solidification process.The coupling agent is silane coupling agent, titanium One of acid esters coupling agent, aluminate coupling agent, bimetallic coupling agent are a variety of.The thermal interfacial material be inorganic material with The composite material of high molecular material, the coupling agent have two kinds of groups of close inorganic material and organic-philic material simultaneously, can incite somebody to action Two kinds of material tights are fused together, at the same play boron nitride heating conduction and thermoset macromolecule material it is heat-resisting, exhausted The function of edge and solid.
The specific silane coupling agent be one of KH550 coupling agent, KH560 coupling agent or KH570 coupling agent or It is a variety of.
The diluent is glycidol ether, preferably n-butyl glycidyl ether, diglycidyl ether, 1,4-butanediol two One of glycidol ether, polyglycidyl ether, trihydroxy methyl propane glycidol ether are a variety of.The diluent is Active glycerin ether diluent, curing reaction can be participated in while reducing system viscosity becomes a part of curing materials, Material property will not be reduced.
The synergistic effect of the various raw materials of the thermal interfacial material is so that the thermal interfacial material has excellent thermal conductivity Also has the advantages that heat-resisting, good insulation preformance while energy.As shown in Fig. 1: the main ingredient of thermal interfacial material includes Polymeric matrix and spherical boron nitride filler, wherein 10 representation polymer matrixes, 20 represent spherical boron nitride filler.Further Scanning electron microscope characterization has been carried out to the spherical boron nitride.It is shown such as attached drawing 2: form of the spherical boron nitride under Electronic Speculum.
Based on above-mentioned thermal interfacial material, the embodiment of the invention also provides a kind of method of preparing heat interfacial material, the system Preparation Method includes the following steps:
S01: by the spherical boron nitride, thermosetting resin, curing agent, defoaming agent, coupling agent and diluent mixed processing;
S02: the processing that is heating and curing obtains thermal interfacial material.
Mixed processing described in specific step S01 is in order to enable each component is uniformly mixed, as can be using routine Hybrid mode mixes each component.It as in a particular embodiment, is handled using ball milling mixing, so that each component is sufficiently mixed It closes uniform.When using ball milling mixing processing, the technological parameter of the ball-milling treatment are as follows: 200~500rpm of ball milling speed;Ball milling Time is 0.5~2h.
In addition, each component each component as described in thermal interfacial material above in step S01, in order to save length, Details are not described herein.
The temperature that is heating and curing described in step S02 is 60-200 DEG C, and the time that is heating and curing is 0.5-6h.Suitable temperature can To promote curing rate, and the strength thermal resistant water resistance of material is effectively promoted, corrosion resistance etc., temperature is too low to lead to solidification not Completely, the performance of material is reduced, temperature is too high to will lead to energy consumption increase, generates unnecessary waste-.
The preparation method of the thermal interfacial material does raw material due to using spherical boron nitride, so that integral material viscosity drops It is low, it becomes prone to process, and more boron nitride can be filled, enhances heating conduction, increase while reducing difficulty of processing The strong performance of the thermal interfacial material.
It is further described combined with specific embodiments below.
Embodiment 1
The present embodiment provides a kind of thermal interfacial material and preparation method thereof, the thermal interfacial material is by including following quality The component of percentage is formed:
Spherical boron nitride: 30%, diameter is 5 μm;
Thermosetting resin: 50% bisphenol A-type liquid epoxy resin;
Curing agent: 4% methyl hexahydrophthalic anhydride and 1% 3-(dimethylamino methyl) phenol;
Coupling agent: 10% KH560 silane coupling agent;
Diluent: 5% n-butyl glycidyl ether.
The method of preparing heat interfacial material includes the following steps:
Above-mentioned raw materials are uniformly mixed using ball-milling technology.Milling parameters are as follows: ball milling speed 500, Ball-milling Time 0.5h.Obtained mixture is solidified into 3h at 200 DEG C and obtains final thermal interfacial material.
Embodiment 2
The present embodiment provides a kind of thermal interfacial material and preparation method thereof, the thermal interfacial material is by including following quality The component of percentage is formed:
Spherical boron nitride: 70%, diameter is 200 μm;
Thermosetting resin: 20% bisphenol F-type epoxy resin;
Curing agent: 4% tetraethylenepentamine and 1%N, N- dimethyl benzylamine;
Coupling agent: 1% KH550 silane coupling agent;
Diluent: 4% 1,4- butanediol diglycidyl ether.
The method of preparing heat interfacial material includes the following steps:
Above-mentioned raw materials are uniformly mixed using ball-milling technology.Milling parameters are as follows: ball milling speed 200, Ball-milling Time 2h. Obtained mixture is solidified into 2h at 200 DEG C and obtains final thermal interfacial material.
Embodiment 3
Spherical boron nitride: 40%, diameter is 100 μm;
Thermosetting resin: 40% alicyclic liquid-state epoxy resin;
Curing agent: 4% m-phenylene diamine (MPD) and 1%N, N- dimethyl benzylamine;
Coupling agent: 1% KH550 silane coupling agent;
Diluent: 4% 1,4- butanediol diglycidyl ether.
The method of preparing heat interfacial material includes the following steps:
Above-mentioned raw materials are uniformly mixed using ball-milling technology.Milling parameters are as follows: ball milling speed 200, Ball-milling Time 2h. Obtained mixture is solidified into 2h at 200 DEG C and obtains final thermal interfacial material.-
Embodiment 4
Spherical boron nitride: 50%, diameter is 50 μm;
Thermosetting resin: 30% bisphenol A-type liquid epoxy resin;
Curing agent: 4% methyl hexahydrophthalic anhydride and 1% 3-(dimethylamino methyl) phenol;
Coupling agent: 10% KH560 silane coupling agent;
Diluent: 5% n-butyl glycidyl ether.
The method of preparing heat interfacial material includes the following steps:
Above-mentioned raw materials are uniformly mixed using ball-milling technology.Milling parameters are as follows: ball milling speed 500, Ball-milling Time 0.5h.Obtained mixture is solidified into 3h at 200 DEG C and obtains final thermal interfacial material.
Embodiment 5
A kind of thermal interfacial material and preparation method thereof, in addition to the spherical boron nitride is 200 μm, other conditions with implementation Example 4 is identical.
And the thermal interfacial material generated to five embodiments has carried out the test of heating conduction:
Table 1
Project Thermal coefficient (W/mK)
Embodiment 1 0.5
Embodiment 2 6.0
Embodiment 3 2.0
Embodiment 4 3.0
Embodiment 5 3.4
The Applicant declares that the present invention is explained by the above embodiments detailed construction feature of the invention, but the present invention is simultaneously It is not limited to above-mentioned detailed construction feature, that is, does not mean that the present invention must rely on above-mentioned detailed construction feature and could implement.Institute Belong to those skilled in the art it will be clearly understood that any improvement in the present invention, to the equivalence replacement of component selected by the present invention And increase, selection of concrete mode of accessory etc., all of which fall within the scope of protection and disclosure of the present invention.
The preferred embodiment of the present invention has been described above in detail, still, during present invention is not limited to the embodiments described above Detail within the scope of the technical concept of the present invention can be with various simple variants of the technical solution of the present invention are made, this A little simple variants all belong to the scope of protection of the present invention.
It is further to note that specific technical features described in the above specific embodiments, in not lance In the case where shield, can be combined in any appropriate way, in order to avoid unnecessary repetition, the present invention to it is various can No further explanation will be given for the combination of energy.
In addition, various embodiments of the present invention can be combined randomly, as long as it is without prejudice to originally The thought of invention, it should also be regarded as the disclosure of the present invention.

Claims (10)

1. a kind of thermal interfacial material, it is characterised in that: the thermal interfacial material is by including that the component of following mass percent carries out It is formed:
2. thermal interfacial material as described in claim 1, it is characterised in that: the diameter of the spherical boron nitride is 5 μm~200 μ m;And/or
The thermosetting resin is liquid epoxies or organic siliconresin.
3. thermal interfacial material according to claim 2, it is characterised in that: the liquid epoxies is bisphenol A-type liquid One of epoxy resin, bisphenol F-type epoxy resin, alicyclic liquid-state epoxy resin are a variety of;And/or
The organic siliconresin is poly- methyl silicon resin, in poly- ethyl silicone resin, polyphenylene silicone resin, polyphenyl methyl silicone resin It is one or more.
4. thermal interfacial material according to claim 1, it is characterised in that: the curing agent is methyl hexahydrophthalic anhydride, tetrem Five amine of alkene, m-phenylene diamine (MPD), 2-ethyl-4-methylimidazole, N, in N- dimethyl benzylamine and three-(dimethylamino methyl) phenol It is one or more;And/or
The coupling agent is one of silane coupling agent, titanate coupling agent, aluminate coupling agent, bimetallic coupling agent or more Kind.
5. thermal interfacial material as claimed in claim 4, it is characterised in that: the silane coupling agent be KH550 coupling agent, One of KH560 coupling agent or KH570 coupling agent are a variety of.
6. thermal interfacial material according to claim 1, it is characterised in that: the diluent is glycidol ether, preferably just Butyl glycidyl ether, diglycidyl ether, 1,4- butanediol diglycidyl ether, polyglycidyl ether, trihydroxy methyl third One of alkane glycidol ether is a variety of.
7. thermal interfacial material according to claim 1-6, it is characterised in that: the thermally conductive system of the thermal interfacial material Number is 0.5-6W/mK.
8. a kind of according to the described in any item method of preparing heat interfacial material of claim 1~7, which is characterized in that including walking as follows It is rapid:
The spherical boron nitride, thermosetting resin, curing agent, defoaming agent, coupling agent and diluent are subjected to mixed processing, formed Mixture;
The mixture processing that be heating and curing is obtained into thermal interfacial material.
9. the preparation method according to requiring 8, it is characterised in that: described be heating and curing as temperature is 60-200 DEG C, and heating is solid The change time is 0.5-6h.
10. the preparation method according to requiring 8 or 9, which is characterized in that it include ball-milling treatment during the mixed processing, The technological parameter of the ball-milling treatment are as follows: 200~500rpm of ball milling speed;Ball-milling Time is 0.5~2h.
CN201810871021.9A 2018-08-02 2018-08-02 Thermal interfacial material and preparation method thereof Pending CN109054302A (en)

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110128997A (en) * 2019-05-17 2019-08-16 陈定方 A kind of organic silicon potting adhesive effectively improving thermal coefficient and preparation method
CN111138832A (en) * 2019-12-16 2020-05-12 湖南文理学院 Method for preparing BN thermal interface material
CN111423699A (en) * 2020-05-12 2020-07-17 河北工业大学 Preparation method of high-filling-amount hexagonal boron nitride/polymer blocky composite material
CN111423698A (en) * 2020-05-12 2020-07-17 河北工业大学 High-filling-amount hexagonal boron nitride nanosheet/fiber/polymer blocky composite material and preparation method thereof
CN111995991A (en) * 2020-07-27 2020-11-27 深圳陶陶科技有限公司 Thermal interface material and preparation method thereof
CN112877039A (en) * 2021-03-05 2021-06-01 江苏晶河电子科技有限公司 High-performance single-component organic silicon modified epoxy heat conduction material and preparation method thereof
WO2022124005A1 (en) * 2020-12-11 2022-06-16 富士フイルム株式会社 Curable composition, thermally conductive material, thermally conductive sheet, and device with thermally conductive layer
CN114752216A (en) * 2022-02-28 2022-07-15 复旦大学 Preparation method of internal stress controlled thermal interface material

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103694636A (en) * 2013-12-10 2014-04-02 中国科学院过程工程研究所 Electric insulating epoxy resin composition, preparation method and use of composition
CN106029561A (en) * 2014-02-05 2016-10-12 三菱化学株式会社 Agglomerated boron nitride particles, production method for agglomerated boron nitride particles, resin composition including agglomerated boron nitride particles, moulded body, and sheet
CN106519581A (en) * 2016-11-29 2017-03-22 华中科技大学 High-heat-conductivity low-viscosity epoxy resin composite, and preparation method and application thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103694636A (en) * 2013-12-10 2014-04-02 中国科学院过程工程研究所 Electric insulating epoxy resin composition, preparation method and use of composition
CN106029561A (en) * 2014-02-05 2016-10-12 三菱化学株式会社 Agglomerated boron nitride particles, production method for agglomerated boron nitride particles, resin composition including agglomerated boron nitride particles, moulded body, and sheet
CN106519581A (en) * 2016-11-29 2017-03-22 华中科技大学 High-heat-conductivity low-viscosity epoxy resin composite, and preparation method and application thereof

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
于占江等: "《摩擦材料生产工艺》", 31 January 2018, 天津工业出版社 *
倪文胜等: "《保温防腐工程实用材料手册》", 31 October 2007, 山西科学技术出版社 *
曾贵玉等: "《微纳米含能材料》", 31 May 2015, 国防工业出版社 *

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110128997A (en) * 2019-05-17 2019-08-16 陈定方 A kind of organic silicon potting adhesive effectively improving thermal coefficient and preparation method
CN111138832A (en) * 2019-12-16 2020-05-12 湖南文理学院 Method for preparing BN thermal interface material
CN111423699A (en) * 2020-05-12 2020-07-17 河北工业大学 Preparation method of high-filling-amount hexagonal boron nitride/polymer blocky composite material
CN111423698A (en) * 2020-05-12 2020-07-17 河北工业大学 High-filling-amount hexagonal boron nitride nanosheet/fiber/polymer blocky composite material and preparation method thereof
CN111423699B (en) * 2020-05-12 2022-11-11 河北工业大学 Preparation method of high-filling-amount hexagonal boron nitride/polymer blocky composite material
CN111423698B (en) * 2020-05-12 2022-11-15 河北工业大学 High-filling-amount hexagonal boron nitride nanosheet/fiber/polymer blocky composite material and preparation method thereof
CN111995991A (en) * 2020-07-27 2020-11-27 深圳陶陶科技有限公司 Thermal interface material and preparation method thereof
CN111995991B (en) * 2020-07-27 2022-01-18 深圳陶陶科技有限公司 Thermal interface material and preparation method thereof
WO2022124005A1 (en) * 2020-12-11 2022-06-16 富士フイルム株式会社 Curable composition, thermally conductive material, thermally conductive sheet, and device with thermally conductive layer
CN112877039A (en) * 2021-03-05 2021-06-01 江苏晶河电子科技有限公司 High-performance single-component organic silicon modified epoxy heat conduction material and preparation method thereof
CN114752216A (en) * 2022-02-28 2022-07-15 复旦大学 Preparation method of internal stress controlled thermal interface material

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Application publication date: 20181221