WO2017091974A1 - B-stageable adhesive composition - Google Patents

B-stageable adhesive composition Download PDF

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Publication number
WO2017091974A1
WO2017091974A1 PCT/CN2015/096105 CN2015096105W WO2017091974A1 WO 2017091974 A1 WO2017091974 A1 WO 2017091974A1 CN 2015096105 W CN2015096105 W CN 2015096105W WO 2017091974 A1 WO2017091974 A1 WO 2017091974A1
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WO
WIPO (PCT)
Prior art keywords
adhesive composition
stageable adhesive
stageable
composition according
epoxy resin
Prior art date
Application number
PCT/CN2015/096105
Other languages
French (fr)
Inventor
Ping Zhou
Lianzhou Chen
Liang Qin
Lin Yang
Qunying LIU
Original Assignee
3M Innovative Properties Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 3M Innovative Properties Company filed Critical 3M Innovative Properties Company
Priority to EP15909491.1A priority Critical patent/EP3383966A4/en
Priority to US15/776,545 priority patent/US20180340106A1/en
Priority to JP2018526935A priority patent/JP6800227B2/en
Priority to PCT/CN2015/096105 priority patent/WO2017091974A1/en
Priority to CN201580084934.0A priority patent/CN108291129B/en
Publication of WO2017091974A1 publication Critical patent/WO2017091974A1/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J163/00Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/62Alcohols or phenols
    • C08G59/621Phenols
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/18Homopolymers or copolymers of nitriles
    • C08L33/20Homopolymers or copolymers of acrylonitrile
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L61/00Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
    • C08L61/04Condensation polymers of aldehydes or ketones with phenols only
    • C08L61/06Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
    • C08L61/14Modified phenol-aldehyde condensates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08L9/02Copolymers with acrylonitrile
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02Non-macromolecular additives
    • C09J11/04Non-macromolecular additives inorganic
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J161/00Adhesives based on condensation polymers of aldehydes or ketones; Adhesives based on derivatives of such polymers
    • C09J161/04Condensation polymers of aldehydes or ketones with phenols only
    • C09J161/06Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
    • C09J161/14Modified phenol-aldehyde condensates
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J9/00Adhesives characterised by their physical nature or the effects produced, e.g. glue sticks
    • 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

Definitions

  • the present invention generally relates to the field of adhesive application, and specifically, relates to a B-stageable adhesive composition used in the field of automobile industry, electronic industry or the like.
  • epoxy resins are widely used to provide an adhesive composition in industrial application, which is used for mirror bonding in automobile industry, high bonding for components in electronic application, transformers in electric application or the like.
  • US Patent Number 5,292,812 discloses an adhesive composition consisting essentially of an epoxy resin; a carboxyl group-containing acrylonitrile-butadiene or methacrylonitrile-butadiene copolymer or a combination thereof; a maleimide compound; and an imidazole compound.
  • the resultant compositions are electrically insulative, thermally resistant, highly capable of fabrication at low pressure and stable storage.
  • Chinese Application CN 101314694 provides an insulative resin paint comprising an epoxy resin; a phenol-formaldehyde resin; an epoxy toughener; a leveling agent; and a diluent.
  • This insulative resin paint has good bonding strength to a silicon steel sheet and high temperature resistance.
  • the present inventors In order to develop a new B-stageable adhesive composition having high tackiness, the present inventors have made intensive study. The present inventors have surprisingly found that when an epoxy resin, a carboxyl terminated butadiene-acrylonitrile copolymer and a polyterpene modified phenol-formaldehyde resin are mixed at a specific ratio, an adhesive composition which has good tackiness and the cured product thereof has good bonding strength may be achieved. Additionally, by adjusting the additives to be added into the adhesive composition, the B-stageable adhesive composition can be developed with additional excellent multi-functional properties, such as flame resistance, thermal conductivity or the like.
  • an aspect of the present invention provides a B-stageable adhesive composition, based on the total weight of the adhesive composition, comprising:
  • the present invention has the following advantageous effects.
  • an epoxy resin a carboxyl terminated butadiene-acrylonitrile copolymer and a polyterpene modified phenol-formaldehyde resin at a specific ratio
  • the prepared adhesive composition may have excellent tackiness.
  • the B-stageable adhesive composition can be developed with additional multi-functional properties, such as flame resistance, thermal conductivity or the like.
  • a B-stageable adhesive composition has the traditional meaning in the field, unless otherwise specifically indicated.
  • B-staging is a process that utilizes heat or UV light to remove the majority of a solvent from an adhesive, thereby allowing the construction to be “staged. ”
  • the adhesive composition can be held for a period of time, without sacrificing the performances thereof.
  • An aspect of the present invention provides a B-stageable adhesive composition, based on the total weight of the adhesive composition, comprising:
  • an epoxy resin is incorporated into the B-stageable adhesive composition to be used as a matrix.
  • the epoxy resin has an epoxy equivalent weight of no more than 1000, preferably no more than 800, and more preferably no more than 500. When the epoxy equivalent weight is no more than 1000, the B-stageable adhesive composition has good tackiness. Based on the total weight of the adhesive composition, the content of the epoxy resin is 13-59 wt%, preferably 35-59 wt%. When the content of the epoxy resin is 13-59 wt%, the B-stageable adhesive composition has good tackiness and the cured product thereof has good bonding strength.
  • the specific kinds of the epoxy resin to be used in the invention are not specifically limited as long as they satisfy the about requirements.
  • the epoxy resin is selected from the group consisting of bisphenol A epoxy resin, bisphenol F epoxy resin, phenolic epoxy resin, glycidyl ether epoxy resin, polyurthane modified epoxy resin and the like.
  • One specific example of the epoxy resin is NPEL 128 (Trade Name) from NAN YA EPOXY CORP (Kunshan Campus) , which is a bisphenol A epoxy resin having the epoxy equivalent weight of 188.
  • the B-stageable adhesive composition comprises a carboxyl terminated butadiene-acrylonitrile (CTBN) copolymer as a toughener.
  • the carboxyl terminated butadiene-acrylonitrile copolymer has a mass average molecular weight of no less than 10000, preferably no less than 100000, and more preferably no less than 200000.
  • the weight average molecular weight of the carboxyl terminated butadiene-acrylonitrile (CTBN) copolymer is in a range of, preferably 100000-400000, and more preferably 200000-300000. When the mass average molecular weight is no less than 10000, the cured product of the B-stageable adhesive composition has good bonding strength.
  • the content of the carboxyl terminated butadiene-acrylonitrile copolymer is 18-69 wt%, preferably 21-48 wt%.
  • the B-stageable adhesive composition has good tackiness and the cured product thereof has good bonding strength.
  • One specific example of the carboxyl terminated butadiene-acrylonitrile copolymer is 1072CGX (Trade Name) from ZEON Corporation, which has a mass average molecular weight of no less than 10000.
  • the B-stageable adhesive composition comprises a polyterpene modified phenol-formaldehyde resin used as a tackifier and a high temperature hardener. Based on the total weight of the adhesive composition, the content of the polyterpene modified phenol-formaldehyde resin is 3-34 wt%, preferably 5-30 wt%, and more preferably 15-28 wt%. When the content of the polyterpene modified phenol-formaldehyde resin is 3-34 wt%, the B-stageable adhesive composition has good tackiness and the cured product thereof has good bonding strength.
  • polyterpene modified phenol-formaldehyde resin is T-803L (Trade Name) from ARAKAWA CHEMICAL INDUSTRIES LTD, which can act as a tackifier and even as a hardener under high temperature treatment.
  • the reaction mechanism of the above three components according to the application may be described as follows.
  • the carboxyl groups in the carboxyl terminated butadiene-acrylonitrile (CTBN) copolymer can react with the epoxy groups in the epoxy resin at low temperature to form a B-stageable film.
  • CTBN used in this article acts as a toughener, and the molecular weight of this CTBN is very high, which had good miscibility with the epoxy resin, and excellent mixable with the fillers.
  • the polyterpene modified phenol-formaldehyde resin has a good compatibility with the epoxy resin, and acts as a tackifier at low temperature to provide the good tackiness, and additionally, it can also act as hardener for the epoxy resin at a higher temperature to provide good bonding strength.
  • additional hardener can be added into the composition, which reacts with the epoxy groups in the epoxy resin at a high temperature to get a fully curing structure so as to improve the high temperature resistance performance of the resultant product.
  • the content of the additional hardener is 0.5-5 wt%.
  • the additional hardener to be used in the invention are not specifically limited, and the hardener is selected from the group consisting of dicyandiamide, 4, 4’ -diaminodiphenylsulfone (DDS) , anhydrides, mercaptans, imidozles, ureas, amides and the like.
  • the hardener is dicyandiamide.
  • Dicy Traffic Name
  • the B-stageable adhesive composition further comprises an inorganic filler for improving the performances of the cured product.
  • the content of the organic filler is 0-70 wt%, preferably 20-60 wt%, and more preferably 30-50 wt%.
  • the inorganic filler comprises one or more of a flame retardant agent, a thermal conductive filler, or the like.
  • the content of the flame retardant agent is 0-40 wt%, preferably 10-40 wt%, and more preferably 20-40 wt%.
  • the flame retardant agent is selected from the group consisting of aluminum hydroxide, phosphates and a mixture thereof. Furthermore, based on the total weight of the adhesive composition, the content of the thermal conductive filler is 0-40 wt%, preferably 20-40 wt%, and more preferably 30-40 wt%.
  • the thermal conductive filler is selected from the group consisting of boron nitride, aluminum hydroxide and a mixture thereof.
  • the specific examples of the flame retardant agent are 140LEO (Trade Name) from Albemarle Corporation and OP935 (Trade Name) from Clariant Coporation.
  • One specific example of the thermal conductive filler is Boron Nitride (BN) (Trade Name) from Dandong Thermal Co. Ltd.
  • the B-stageable adhesive composition further comprises a solvent for dissolving the above components.
  • a solvent for dissolving the above components there is no limitation about the specific kinds of the solvent as long as the above components may be fully dissolved therein.
  • the solvent may be selected from the group consisting of butanone, acetone, N, N-dimethyl acetamide, toluene and the like. Most preferably, the solvent is butanone. Based on the total weight of the adhesive composition, the content of the solvent is 20-70 wt%, preferably 20-50 wt%, and more preferably 30-50wt%.
  • the method for preparing the B-stageable adhesive composition comprising the step of mixing the components of the B-stageable adhesive composition provided in the present invention.
  • the temperature of the mixing step is 5-60°C, and the pressure of the mixing step is 0.5-2 atm.
  • the B-stageable adhesive compositions prepared according to the following different preparing conditions were subjected to various tests for verifying the performances thereof in terms of Initial Tackiness, Over Lap Shear (OLS) strength, T-Peel strength, Flame Resistance, and Thermal Conductivity.
  • OLS Over Lap Shear
  • Tackiness is an important performance of the B-stageable adhesive composition and a good initial tackiness can allow the B-stageable adhesive film to be easily provided at a prescribed position at room temperature, and then cured at an elevated temperature without additional pressure, so as to form a cured structure having a good bonding strength.
  • Tackiness is evaluated in the application by measuring the 180 degree peel strength under room temperature (25°C) , according to ASTM D1000. Specifically, a sample of the adhesive film formed by a B-stageable adhesive composition is laminated on a 1mil polyimide (PI) film (HV-25, Rayitek Film Company) at room temperature. The laminated structure is then cut into a size with a width of 0.5 inch, and the adhesion strength thereof is measured on a SUS substrate (304#, ChemInstrument Company) according to ASTM D 1000.
  • PI 1mil polyimide
  • a sample of the adhesive film formed by a B-stageable adhesive composition is tested for T-Peel strength according to ASTM D1002. Specifically, a sample of a B-stageable adhesive film obtained from the B-stageable adhesive composition is adhered to a copper substrate having a thickness of 0.3 mm with manual pressure, and then put into an oven at 185°C to be cured for 40 minutes without pressure. Then, according to ASTM D1002, the T-peel performances are tested under a room temperature (25°C) , under the following conditions: Substrate: copper; Speed: 50mm/min; Sample size: 1inch 2 .
  • T-Peel strength test the value of T-Peel strength test of the cured product of the B-stageable adhesive composition was measured according to the following standards showed in Table 2.
  • the B-stageable adhesive composition is tested for Flame Resistance according to UL94. Specifically, specimens are cut to be 125 ⁇ 5 mm long by 13.0 ⁇ 0.5 mm wide. Before testing, Specimens are preconditioned at 23 ⁇ 2°C and 50 ⁇ 5%relative humidity for a minimum of 48 hours. Five samples are tested, and each sample was under fire (fire height 2mm) for 10s. The afterflame time for each individual specimen is less than 10s, and the total afterflame time for five samples is less than 50s.
  • this standard can be clarified as UL94V0, V1, V0, and when the value of Flame Resistance is UL94V0, the corresponding B-stageable adhesive composition can be regarded as “acceptable” for some special application.
  • the B-stageable adhesive composition is tested for Thermal Conductivity according to ASTM D5470.
  • the slurry was coated on a release liner BY-1 from Bao Yao Company to get an adhesive film having a thickness of about 0.25 mm. Then, the obtained laminated structure was put into an oven at 110°C and dried for 10-15 minutes to dry out the solvent.
  • the adhesive film was peeled from the release liner and used as Sample 1 for further testing.
  • Example 1 22 g 20 g 3 g 7 g 13 g 34 g 1 g 100%
  • Example 2 22 g 20 g 5 g 7 g 13 g 33 g 1 g 100%
  • Example 3 21 g 19 g 9 g 6 g 13 g 31 g 1 g 100%
  • Example 4 20 g 18 g 12 g 6 g 12 g 30 g 1 g 100%
  • Example 5 36 g 32 g 30 g 0 g 0 g 0 g 2 g 100%
  • Example 6 37 g 34 g 27 g 0 g 0 g 0 g 2 g 100%
  • Example 7 49 g 28 g 20 g 0 g 0 g 0 g 3 g 100%
  • Example 8 35 g 48 g 15 g 0 g 0 g 0 g 2 g 100%
  • Example 9 18 g 49 g 31 g 0 g 0 g 0 g g g g g g
  • the B-stageable adhesive composition provided in the present invention has good tackiness and the cured product thereof has good bonding strength.
  • the B-stageable adhesive composition has very good tackiness and the cured product thereof has very good bonding strength.
  • the amount of the epoxy resin is too low, the amount of the polyterpene modified phenol-formaldehyde resin is too high, and therefore, neither the tackiness of the adhesive composition, nor the bonding strength of the cured product of the adhesive composition is acceptable.
  • the amount of the polyterpene modified phenol-formaldehyde resin is too low, therefore the bonding strength of the cured product of the adhesive composition is not acceptable.
  • the amount of the epoxy resin is too low, the amount of the carboxyl terminated butadiene-acrylonitrile copolymer is too high, and therefore, neither the tackiness of the adhesive composition, nor the bonding strength of the cured product of the adhesive composition is acceptable.
  • the amount of the epoxy resin is too low, the amount of the carboxyl terminated butadiene-acrylonitrile copolymer is too high, and therefore, the tackiness of the adhesive composition, is not acceptable.
  • the amount of the epoxy resin is too high, the amount of the carboxyl terminated butadiene-acrylonitrile copolymer is too low, and therefore, the cured product of the adhesive composition after being cured was too brittle to form a film.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • Combustion & Propulsion (AREA)
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  • Inorganic Chemistry (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

The invention provides a B-stageable adhesive composition, based on the total weight of the adhesive composition, comprising: 13-59 wt% of an epoxy resin; 18-69 wt%of a carboxyl terminated butadiene-acrylonitrile copolymer; and 3-34 wt%of a polyterpene modified phenol-formaldehyde resin. Additionally, the B-stageable adhesive composition may further comprise a hardener, an inorganic filler including a flame retardant agent, a thermal conductive filler or the like. According to the disclosure of the application, a new B-stageable adhesive composition having a high tackiness, a high temperature resistance, a high flame resistance and a high thermal conductivity can be provided.

Description

B-STAGEABLE ADHESIVE COMPOSITION FIELD OF THE INVENTION
The present invention generally relates to the field of adhesive application, and specifically, relates to a B-stageable adhesive composition used in the field of automobile industry, electronic industry or the like.
BACKGROUND OF THE INVENTION
Due to the good bonding strength on different substrates and high temperature resistance or the like, epoxy resins are widely used to provide an adhesive composition in industrial application, which is used for mirror bonding in automobile industry, high bonding for components in electronic application, transformers in electric application or the like.
The attempt to use the traditional epoxy adhesives in the above technical fields often creates expensive production bottlenecks, because, as soon as the epoxy adhesives are applied, the applied components had to be assembled and cured immediately. In order to overcome this defect, various B-stageable adhesives have been widely utilized. The B-stageable adhesives eliminate these bottlenecks by allowing the manufacturing process to be proceed efficiently, with each step performed on larger batches of product.
For example, US Patent Number 5,292,812 discloses an adhesive composition consisting essentially of an epoxy resin; a carboxyl group-containing acrylonitrile-butadiene or methacrylonitrile-butadiene copolymer or a combination thereof; a maleimide compound; and an imidazole compound. The resultant compositions are electrically insulative, thermally resistant, highly capable of fabrication at low pressure and stable storage.
Additionally, Chinese Application CN 101314694 provides an insulative resin paint comprising an epoxy resin; a phenol-formaldehyde resin; an epoxy toughener; a leveling agent; and a diluent. This insulative resin paint has good bonding strength to a silicon steel sheet and high temperature resistance.
However, when a B-stageable adhesive composition is produced for the above  applications, because of the poor tackiness between the various substrates and a B-stageable adhesive film, the customer needs to clamp the adhesive film at a prescribed position and develop the bonding strength at an elevating temperature so as to get a fully curing structure. It is an energy-cost for heating and very complex assembling process for the customer.
Therefore, there is a need to develop a new B-stageable adhesive composition having high tackiness, which can be easily provided at a prescribed position at room temperature, and then cured at an elevated temperature without additional pressure, so as to form a cured structure having a good bonding strength. With these benefits, it can further simplify the customer operation process, and achieve the improved product reliability and the productivity of customer process.
SUMMARY OF THE INVENTION
In order to develop a new B-stageable adhesive composition having high tackiness, the present inventors have made intensive study. The present inventors have surprisingly found that when an epoxy resin, a carboxyl terminated butadiene-acrylonitrile copolymer and a polyterpene modified phenol-formaldehyde resin are mixed at a specific ratio, an adhesive composition which has good tackiness and the cured product thereof has good bonding strength may be achieved. Additionally, by adjusting the additives to be added into the adhesive composition, the B-stageable adhesive composition can be developed with additional excellent multi-functional properties, such as flame resistance, thermal conductivity or the like.
Therefore, an aspect of the present invention provides a B-stageable adhesive composition, based on the total weight of the adhesive composition, comprising:
13-59 wt%of an epoxy resin;
18-69 wt%of a carboxyl terminated butadiene-acrylonitrile copolymer; and
3-34 wt%of a polyterpene modified phenol-formaldehyde resin.
The present invention has the following advantageous effects. By specifically selecting an epoxy resin, a carboxyl terminated butadiene-acrylonitrile copolymer and a polyterpene modified phenol-formaldehyde resin at a specific ratio, the prepared adhesive composition may have excellent tackiness. Additionally, by adjusting the additives to be  added into the adhesive composition, the B-stageable adhesive composition can be developed with additional multi-functional properties, such as flame resistance, thermal conductivity or the like.
DETAILED DESCRIPTION OF THE INVENTION
In the present invention, the term “a B-stageable adhesive composition” has the traditional meaning in the field, unless otherwise specifically indicated. B-staging is a process that utilizes heat or UV light to remove the majority of a solvent from an adhesive, thereby allowing the construction to be “staged. ” In between the processes of coating, assembling and curing of the adhesive composition, the adhesive composition can be held for a period of time, without sacrificing the performances thereof.
An aspect of the present invention provides a B-stageable adhesive composition, based on the total weight of the adhesive composition, comprising:
13-59 wt%of an epoxy resin;
18-69 wt%of a carboxyl terminated butadiene-acrylonitrile copolymer; and
3-34 wt%of a polyterpene modified phenol-formaldehyde resin.
According to certain embodiments of the present invention, an epoxy resin is incorporated into the B-stageable adhesive composition to be used as a matrix. The epoxy resin has an epoxy equivalent weight of no more than 1000, preferably no more than 800, and more preferably no more than 500. When the epoxy equivalent weight is no more than 1000, the B-stageable adhesive composition has good tackiness. Based on the total weight of the adhesive composition, the content of the epoxy resin is 13-59 wt%, preferably 35-59 wt%. When the content of the epoxy resin is 13-59 wt%, the B-stageable adhesive composition has good tackiness and the cured product thereof has good bonding strength. The specific kinds of the epoxy resin to be used in the invention are not specifically limited as long as they satisfy the about requirements. According to certain embodiments of the present invention, the epoxy resin is selected from the group consisting of bisphenol A epoxy resin, bisphenol F epoxy resin, phenolic epoxy resin, glycidyl ether epoxy resin, polyurthane modified epoxy resin and the like. One specific example of the epoxy resin is  NPEL 128 (Trade Name) from NAN YA EPOXY CORP (Kunshan Campus) , which is a bisphenol A epoxy resin having the epoxy equivalent weight of 188.
According to certain embodiments of the present invention, the B-stageable adhesive composition comprises a carboxyl terminated butadiene-acrylonitrile (CTBN) copolymer as a toughener. The carboxyl terminated butadiene-acrylonitrile copolymer has a mass average molecular weight of no less than 10000, preferably no less than 100000, and more preferably no less than 200000. The weight average molecular weight of the carboxyl terminated butadiene-acrylonitrile (CTBN) copolymer is in a range of, preferably 100000-400000, and more preferably 200000-300000. When the mass average molecular weight is no less than 10000, the cured product of the B-stageable adhesive composition has good bonding strength. Based on the total weight of the adhesive composition, the content of the carboxyl terminated butadiene-acrylonitrile copolymer is 18-69 wt%, preferably 21-48 wt%. When the content of the carboxyl terminated butadiene-acrylonitrile copolymer is 18-69 wt%, the B-stageable adhesive composition has good tackiness and the cured product thereof has good bonding strength. One specific example of the carboxyl terminated butadiene-acrylonitrile copolymer is 1072CGX (Trade Name) from ZEON Corporation, which has a mass average molecular weight of no less than 10000.
According to certain embodiments of the present invention, the B-stageable adhesive composition comprises a polyterpene modified phenol-formaldehyde resin used as a tackifier and a high temperature hardener. Based on the total weight of the adhesive composition, the content of the polyterpene modified phenol-formaldehyde resin is 3-34 wt%, preferably 5-30 wt%, and more preferably 15-28 wt%. When the content of the polyterpene modified phenol-formaldehyde resin is 3-34 wt%, the B-stageable adhesive composition has good tackiness and the cured product thereof has good bonding strength. One specific example of the polyterpene modified phenol-formaldehyde resin is T-803L (Trade Name) from ARAKAWA CHEMICAL INDUSTRIES LTD, which can act as a tackifier and even as a hardener under high temperature treatment.
The reaction mechanism of the above three components according to the application may be described as follows. The carboxyl groups in the carboxyl terminated butadiene-acrylonitrile (CTBN) copolymer can react with the epoxy groups in the epoxy resin at low  temperature to form a B-stageable film. Meanwhile, CTBN used in this article acts as a toughener, and the molecular weight of this CTBN is very high, which had good miscibility with the epoxy resin, and excellent mixable with the fillers. Furthermore, the polyterpene modified phenol-formaldehyde resin has a good compatibility with the epoxy resin, and acts as a tackifier at low temperature to provide the good tackiness, and additionally, it can also act as hardener for the epoxy resin at a higher temperature to provide good bonding strength.
During the curing process of the B-stageable adhesive composition, additional hardener can be added into the composition, which reacts with the epoxy groups in the epoxy resin at a high temperature to get a fully curing structure so as to improve the high temperature resistance performance of the resultant product. Based on the total weight of the adhesive composition, the content of the additional hardener is 0.5-5 wt%. The specific kinds of the additional hardener to be used in the invention are not specifically limited, and the hardener is selected from the group consisting of dicyandiamide, 4, 4’ -diaminodiphenylsulfone (DDS) , anhydrides, mercaptans, imidozles, ureas, amides and the like. Preferably, the hardener is dicyandiamide. One specific example of dicyandiamide is Dicy (Trade Name) from NINGXIA DARONG CHEMCIALS &METALLURY CO. LTD.
According to certain embodiments of the present invention, in addition to the above components, the B-stageable adhesive composition further comprises an inorganic filler for improving the performances of the cured product. Based on the total weight of the adhesive composition, the content of the organic filler is 0-70 wt%, preferably 20-60 wt%, and more preferably 30-50 wt%. Specifically, the inorganic filler comprises one or more of a flame retardant agent, a thermal conductive filler, or the like. Based on the total weight of the adhesive composition, the content of the flame retardant agent is 0-40 wt%, preferably 10-40 wt%, and more preferably 20-40 wt%. The flame retardant agent is selected from the group consisting of aluminum hydroxide, phosphates and a mixture thereof. Furthermore, based on the total weight of the adhesive composition, the content of the thermal conductive filler is 0-40 wt%, preferably 20-40 wt%, and more preferably 30-40 wt%. The thermal conductive filler is selected from the group consisting of boron nitride, aluminum hydroxide and a mixture thereof. The specific examples of the flame retardant agent are 140LEO (Trade Name) from Albemarle Corporation and OP935 (Trade Name) from Clariant  Coporation. One specific example of the thermal conductive filler is Boron Nitride (BN) (Trade Name) from Dandong Thermal Co. Ltd.
According to certain embodiments of the present invention, the B-stageable adhesive composition further comprises a solvent for dissolving the above components. There is no limitation about the specific kinds of the solvent as long as the above components may be fully dissolved therein. Preferably, the solvent may be selected from the group consisting of butanone, acetone, N, N-dimethyl acetamide, toluene and the like. Most preferably, the solvent is butanone. Based on the total weight of the adhesive composition, the content of the solvent is 20-70 wt%, preferably 20-50 wt%, and more preferably 30-50wt%.
The method for preparing the B-stageable adhesive composition comprising the step of mixing the components of the B-stageable adhesive composition provided in the present invention.
According to certain embodiments of the present invention, the temperature of the mixing step is 5-60℃, and the pressure of the mixing step is 0.5-2 atm.
Testing Methods:
In the present invention, the B-stageable adhesive compositions prepared according to the following different preparing conditions were subjected to various tests for verifying the performances thereof in terms of Initial Tackiness, Over Lap Shear (OLS) strength, T-Peel strength, Flame Resistance, and Thermal Conductivity.
The testing methods for the above characteristics are as follows:
1. Tackiness
Tackiness is an important performance of the B-stageable adhesive composition and a good initial tackiness can allow the B-stageable adhesive film to be easily provided at a prescribed position at room temperature, and then cured at an elevated temperature without additional pressure, so as to form a cured structure having a good bonding strength. Tackiness is evaluated in the application by measuring the 180 degree peel strength under room temperature (25℃) , according to ASTM D1000. Specifically, a sample of the adhesive film formed by a B-stageable adhesive composition is laminated on a 1mil polyimide (PI)  film (HV-25, Rayitek Film Company) at room temperature. The laminated structure is then cut into a size with a width of 0.5 inch, and the adhesion strength thereof is measured on a SUS substrate (304#, ChemInstrument Company) according to ASTM D 1000.
In the tackiness test, the ATS value of the B-stageable adhesive composition was measured according to the following standards showed in Table 1.
Table 1
ATS Tackiness
0.1-0.5 N/mm Good
0.5-1.0 N/mm Verv Good
≥1.0N/mm Excellent
2. T-Peel strength
In order to investigate the bonding strength of the finally cured product formed by the B-stageable adhesive composition, a sample of the adhesive film formed by a B-stageable adhesive composition is tested for T-Peel strength according to ASTM D1002. Specifically, a sample of a B-stageable adhesive film obtained from the B-stageable adhesive composition is adhered to a copper substrate having a thickness of 0.3 mm with manual pressure, and then put into an oven at 185℃ to be cured for 40 minutes without pressure. Then, according to ASTM D1002, the T-peel performances are tested under a room temperature (25℃) , under the following conditions: Substrate: copper; Speed: 50mm/min; Sample size: 1inch2.
In the T-Peel strength test, the value of T-Peel strength test of the cured product of the B-stageable adhesive composition was measured according to the following standards showed in Table 2.
Table 2
T-Peel Strength Bonding Strength
0.3-0.8 N/mm Good
0.8-1.1 N/mm Verv Good
≥1.1 N/mm Excellent
3. Flame Resistance
In order to investigate the Flame Resistance of the finally cured product formed by the B-stageable adhesive composition, the B-stageable adhesive composition is tested for  Flame Resistance according to UL94. Specifically, specimens are cut to be 125±5 mm long by 13.0±0.5 mm wide. Before testing, Specimens are preconditioned at 23±2℃ and 50±5%relative humidity for a minimum of 48 hours. Five samples are tested, and each sample was under fire (fire height 2mm) for 10s. The afterflame time for each individual specimen is less than 10s, and the total afterflame time for five samples is less than 50s.
With regard to the experimental data achieved in the above process, this standard can be clarified as UL94V0, V1, V0, and when the value of Flame Resistance is UL94V0, the corresponding B-stageable adhesive composition can be regarded as “acceptable” for some special application.
4. Thermal Conductivity
In order to investigate the Thermal Conductivity of the finally cured product formed by the B-stageable adhesive composition, the B-stageable adhesive composition is tested for Thermal Conductivity according to ASTM D5470.
With regard to the experimental data achieved in the above process, when the value of Thermal Conductivity is 0.8 W/m. K, the corresponding B-stageable adhesive composition is “acceptable” for some special application.
Examples
The present invention is further illustrated by the following examples which should not be construed to limit the scope of the present invention. All parts and percentages are by weight unless otherwise indicated.
The following raw materials as shown in Table 3 were used for the examples in the examples of present invention.
Table 3
Figure PCTCN2015096105-appb-000001
The chemical reagents in addition to the reagents listed in Table 3 are all from the common commercial sources.
Example 1
At 23 ℃, 7 g of 104LEO, 13 g of OP935, and 34 g of BN were dispersed into butanone to form slurry. After stirring the slurry for 15 minutes, 22 g ofNPEL128, 3 g of T803L, 1 g of Dicy and 20 g of 1072CGX were added into the slurry. The slurry was mixed for 15-20 minutes. At the same time, additional butanone was added into the slurry to adjust the solid contents ofNPEL128, 1072CGX, T803L, 140LEO, OP935, BN, and Dicy to be 22 wt%, 20 wt%, 3 wt%, 7 wt%, 13 wt%, 34 wt%, and 1 wt%based on the total weight of the final slurry, respectively.
Then, the slurry was coated on a release liner BY-1 from Bao Yao Company to get an adhesive film having a thickness of about 0.25 mm. Then, the obtained laminated structure was put into an oven at 110℃ and dried for 10-15 minutes to dry out the solvent.
The adhesive film was peeled from the release liner and used as Sample 1 for further testing.
Examples 2-14 and Comparative Example 1-5
Different adhesive films were prepared by following the same procedure under the same conditions as described in Example 1, except that the contents of respective  components were selected as shown in Table 4.
Table 4
Examples NPEL128 1072CGX T-803L 104LEO OP935 BN Dicv Sum
Example 1 22 g 20 g 3 g 7 g 13 g 34 g 1 g 100%
Example 2 22 g 20 g 5 g 7 g 13 g 33 g 1 g 100%
Example 3 21 g 19 g 9 g 6 g 13 g 31 g 1 g 100%
Example 4 20 g 18 g 12 g 6 g 12 g 30 g 1 g 100%
Example 5 36 g 32 g 30 g 0 g 0 g 0 g 2 g 100%
Example 6 37 g 34 g 27 g 0 g 0 g 0 g 2 g 100%
Example 7 49 g 28 g 20 g 0 g 0 g 0 g 3 g 100%
Example 8 35 g 48 g 15 g 0 g 0 g 0 g 2 g 100%
Example 9 18 g 49 g 31 g 0 g 0 g 0 g 1 g 100%
Example 10 13 g 53 g 34 g 0 g 0 g 0 g 1 g 100%
Example 11 59 g 21 g 20 g 0 g 0 g 0 g 0 g 100%
Example 12 48 g 49 g 3 g 0 g 0 g 0 g 0 g 100%
Example 13 11 g 65 g 24 g 0 g 0 g 0 g 0 g 100%
Example 14 42 g 30 g 28 g 0 g 0 g 0 g 0 g 100%
Comparative Example 1 8 g 56 g 36 g 0 g 0 g 0 g 0% 100%
Comparative Example 2 49 g 49 g 1 g 0 g 0 g 0 g 0% 100%
Comparative Example 3 5 g 72 g 24 g 0 g 0 g 0 g 0% 100%
Comparative Example 4 8 g 69 g 23 g 0 g 0 g 0 g 0% 100%
Comparative Example 5 66 g 15 g 20 g 0 g 0 g 0 g 0% 100%
The samples 1-14 and C1-C5 of the adhesive films prepared in Examples 1-14 and Comparative Example 1-5 were subjected to the tests for verifying the performances thereof in terms of Initial Tackiness, T-Peel strength, Flame Resistance, and Thermal Conductivity according to the Testing Methods as described above. The obtained results thereof were shown in Table 5.
Table 5
Figure PCTCN2015096105-appb-000002
Figure PCTCN2015096105-appb-000003
According to the Examples 1-14, Comparative Example 1-5 and the test results thereof shown in Tables 4 and 5, the B-stageable adhesive composition provided in the present invention has good tackiness and the cured product thereof has good bonding strength.
Especially, according to the Example 6, 7, 8, 11 and 14, when the amount of the epoxy resin is 35-59 wt%, the amount of the carboxyl terminated butadiene-acrylonitrile copolymer is 21-48 wt%, and the amount of the polyterpene modified phenol-formaldehyde resin is 15-28 wt%, the B-stageable adhesive composition has very good tackiness and the cured product thereof has very good bonding strength.
According to the Comparative Example 1, the amount of the epoxy resin is too low, the amount of the polyterpene modified phenol-formaldehyde resin is too high, and therefore, neither the tackiness of the adhesive composition, nor the bonding strength of the cured product of the adhesive composition is acceptable.
According to the Comparative Example 2, the amount of the polyterpene modified phenol-formaldehyde resin is too low, therefore the bonding strength of the cured product of the adhesive composition is not acceptable.
According to the Comparative Example 3, the amount of the epoxy resin is too low, the amount of the carboxyl terminated butadiene-acrylonitrile copolymer is too high, and therefore, neither the tackiness of the adhesive composition, nor the bonding strength of the cured product of the adhesive composition is acceptable.
According to the Comparative Example 4, the amount of the epoxy resin is too low, the amount of the carboxyl terminated butadiene-acrylonitrile copolymer is too high, and therefore, the tackiness of the adhesive composition, is not acceptable.
According to the Comparative Example 5, the amount of the epoxy resin is too high,  the amount of the carboxyl terminated butadiene-acrylonitrile copolymer is too low, and therefore, the cured product of the adhesive composition after being cured was too brittle to form a film.
Although the invention is described with reference to the examples in detail, it is noted that the invention is not limited to the examples. The invention can be changed or modified without departing from the spirit of the invention.

Claims (17)

  1. A B-stageable adhesive composition, based on the total weight of the adhesive composition, comprising:
    13-59 wt% of an epoxy resin;
    18-69 wt% of a carboxyl terminated butadiene-acrylonitrile copolymer; and
    3-34 wt% of a polyterpene modified phenol-formaldehyde resin.
  2. The B-stageable adhesive composition according to claim 1, wherein the epoxy resin has an epoxy equivalent weight of no more than 1000.
  3. The B-stageable adhesive composition according to claim 1, wherein the epoxy resin is selected from the group consisting of bisphenol A epoxy resin, bisphenol F epoxy resin, phenolic epoxy resin, glycidyl ether epoxy resin, and polyurthane modified epoxy resin.
  4. The B-stageable adhesive composition according to claim 1, wherein the content of the epoxy resin is 35-59 wt%.
  5. The B-stageable adhesive composition according to claim 1, wherein the carboxyl terminated butadiene-acrylonitrile copolymer has a mass average molecular weight of no less than 10000.
  6. The B-stageable adhesive composition according to claim 1, wherein the content of the carboxyl terminated butadiene-acrylonitrile copolymer is 21-48 wt%.
  7. The B-stageable adhesive composition according to claim 1, wherein the content of the polyterpene modified phenol-formaldehyde resin is15-28 wt%.
  8. The B-stageable adhesive composition according to claim 1, wherein the B-stageable adhesive composition further comprises 0.5-5 wt% of a hardener.
  9. The B-stageable adhesive composition according to claim 8, wherein the hardener is selected from the group consisting of dicyandiamide, 4, 4’ -diaminodiphenylsulfone, anhydrides, mercaptans, imidozles, ureas, and amides.
  10. The B-stageable adhesive composition according to claim 8, wherein the hardener is dicyandiamide.
  11. The B-stageable adhesive composition according to claim 1, wherein the B- stageable adhesive composition comprises 0.5-5 wt% of dicyandiamide based on the total weight of the adhesive composition.
  12. The B-stageable adhesive composition according to claim 1, wherein the B-stageable adhesive composition further comprises 0-70 wt% of an inorganic filler based on the total weight of the adhesive composition.
  13. The B-stageable adhesive composition according to claim 12, wherein the inorganic filler comprises one or more of a flame retardant agent and a thermal conductive filler.
  14. The B-stageable adhesive composition according to claim 1, wherein the B-stageable adhesive composition further comprises 0-40 wt% of a flame retardant agent selected from the group consisting of aluminum hydroxide, phosphates and a mixture thereof.
  15. The B-stageable adhesive composition according to claim 1, wherein the B-stageable adhesive composition further comprises 0-40 wt% of a thermal conductive filler selected from the group consisting of boron nitride, aluminum hydroxide and a mixture thereof.
  16. The B-stageable adhesive composition according to claim 1, wherein the B-stageable adhesive composition further comprises a solvent.
  17. The B-stageable adhesive composition according to claim 16, wherein the solvent is butanone.
PCT/CN2015/096105 2015-12-01 2015-12-01 B-stageable adhesive composition WO2017091974A1 (en)

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US15/776,545 US20180340106A1 (en) 2015-12-01 2015-12-01 B-stageable adhesive composition
JP2018526935A JP6800227B2 (en) 2015-12-01 2015-12-01 B-staged adhesive composition
PCT/CN2015/096105 WO2017091974A1 (en) 2015-12-01 2015-12-01 B-stageable adhesive composition
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2574223A (en) * 2018-05-30 2019-12-04 Acell Ind Ltd Adhesives and methods of forming adhesives
WO2020236440A1 (en) 2019-05-21 2020-11-26 Ddp Specialty Electronic Materials Us, Llc Two-part interface materials, systems including the interface material, and methods thereof
WO2020236384A1 (en) 2019-05-21 2020-11-26 Ddp Specialty Electronic Materials Us, Llc Thermal interface materials

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114929827A (en) * 2019-12-27 2022-08-19 3M创新有限公司 High temperature resistant B-stageable epoxy adhesives and articles made therefrom
CN112048250A (en) * 2020-08-14 2020-12-08 上海文施绿极科技有限公司 Fast curing adhesive tape for fuel cell and method for manufacturing the same

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6357686A (en) * 1986-08-29 1988-03-12 Yokohama Rubber Co Ltd:The Thermosetting adhesive tape
EP0361754A1 (en) * 1988-09-20 1990-04-04 Hitachi Chemical Co., Ltd. Adhesive composition for printed wiring boards
CN101974205A (en) * 2010-08-20 2011-02-16 广东生益科技股份有限公司 Resin composition for embedded capacitor, and dielectric layer and metal foil-clad plate manufactured by using same
CN102051151A (en) * 2009-11-04 2011-05-11 第一毛织株式会社 Liquid adhesive composition of semiconductor device and semiconductor device using the same
CN102181238A (en) * 2011-04-19 2011-09-14 三友(天津)高分子技术有限公司 Heat-cured high-intensity flaky adhesive for automobile and preparation method thereof

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6369255A (en) * 1986-09-10 1988-03-29 Hitachi Ltd Semiconductor device
JP2605423B2 (en) * 1988-09-20 1997-04-30 日立化成工業株式会社 Adhesive for printed wiring boards
JP2572293B2 (en) * 1990-05-23 1997-01-16 油化シェルエポキシ株式会社 Epoxy resin curing agent and curable epoxy resin composition
JPH04189886A (en) * 1990-11-22 1992-07-08 Modern Plast Kogyo Kk Thermosetting tacky adhesive composition
JPH09181128A (en) * 1995-12-25 1997-07-11 Bando Chem Ind Ltd Manufacture of adhesive tape for semiconductor
JPH09183878A (en) * 1995-12-28 1997-07-15 Nippon Steel Chem Co Ltd Phenolic resin and styrene resin composition compounded with the phenolic resin
JPH10178053A (en) * 1996-10-15 1998-06-30 Toray Ind Inc Adhesive composition for semiconductor device and adhesive sheet for semiconductor device using the same
JP2002037983A (en) * 2000-07-27 2002-02-06 Mitsui Chemicals Inc Epoxy resin composition
JP2002180021A (en) * 2000-12-19 2002-06-26 Hitachi Chem Co Ltd Adhesive composition, adhesive film given by using the same, semiconductor chip-mounting substrate, and semiconductor device given by using the film
JP3936214B2 (en) * 2002-03-25 2007-06-27 株式会社東芝 Resin composition
EP2065383A1 (en) * 2003-11-19 2009-06-03 Signal Pharmaceuticals, Inc. Indazole compounds and methods of use thereof as protein kinase inhibitors
KR100637322B1 (en) * 2004-10-22 2006-10-20 도레이새한 주식회사 Adhesive tape composition for electronic components
KR101152040B1 (en) * 2004-11-30 2012-07-23 스미토모 베이클라이트 가부시키가이샤 Epoxy resin composition and semiconductor device
JP4672505B2 (en) * 2005-04-13 2011-04-20 信越化学工業株式会社 Flame-retardant adhesive composition, and adhesive sheet, coverlay film and flexible copper-clad laminate using the same
DE102005026191A1 (en) * 2005-06-06 2006-12-07 Tesa Ag Heat-activatable films for fixing metal parts on plastics
JP2009007424A (en) * 2007-06-27 2009-01-15 Shin Etsu Chem Co Ltd Adhesive composition, and adhesive sheet and cover lay film using the same
KR101538193B1 (en) * 2008-02-15 2015-07-20 가부시키가이샤 구라레 Curable resin composition and cured resin
CN100564466C (en) * 2008-06-29 2009-12-02 金坛市华荣绝缘材料厂 Special resin paint for epoxy phenolic silicon steel sheet and preparation method thereof
EP2700683B1 (en) * 2012-08-23 2016-06-08 3M Innovative Properties Company Structural adhesive film
RU2608525C2 (en) * 2012-09-29 2017-01-19 3М Инновейтив Пропертиз Компани Adhesive composition and adhesive tape
CN104017528B (en) * 2014-06-20 2016-04-27 合肥长城制冷科技有限公司 Tackiness agent of a kind of bonding copper pipe and aluminium sheet and preparation method thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6357686A (en) * 1986-08-29 1988-03-12 Yokohama Rubber Co Ltd:The Thermosetting adhesive tape
EP0361754A1 (en) * 1988-09-20 1990-04-04 Hitachi Chemical Co., Ltd. Adhesive composition for printed wiring boards
CN102051151A (en) * 2009-11-04 2011-05-11 第一毛织株式会社 Liquid adhesive composition of semiconductor device and semiconductor device using the same
CN101974205A (en) * 2010-08-20 2011-02-16 广东生益科技股份有限公司 Resin composition for embedded capacitor, and dielectric layer and metal foil-clad plate manufactured by using same
CN102181238A (en) * 2011-04-19 2011-09-14 三友(天津)高分子技术有限公司 Heat-cured high-intensity flaky adhesive for automobile and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP3383966A4 *

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2574223A (en) * 2018-05-30 2019-12-04 Acell Ind Ltd Adhesives and methods of forming adhesives
GB2574223B (en) * 2018-05-30 2023-03-01 Acell Ind Ltd Adhesives and methods of forming adhesives
US12104095B2 (en) 2018-05-30 2024-10-01 Acell Industries Limited Adhesives and methods of forming adhesives
WO2020236440A1 (en) 2019-05-21 2020-11-26 Ddp Specialty Electronic Materials Us, Llc Two-part interface materials, systems including the interface material, and methods thereof
WO2020236384A1 (en) 2019-05-21 2020-11-26 Ddp Specialty Electronic Materials Us, Llc Thermal interface materials

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JP2019502780A (en) 2019-01-31
US20180340106A1 (en) 2018-11-29
EP3383966A1 (en) 2018-10-10
CN108291129A (en) 2018-07-17

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