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WO1993020123A1 - A high performance epoxy based laminating adhesive - Google Patents

A high performance epoxy based laminating adhesive Download PDF

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Publication number
WO1993020123A1
WO1993020123A1 PCT/US1993/002677 US9302677W WO9320123A1 WO 1993020123 A1 WO1993020123 A1 WO 1993020123A1 US 9302677 W US9302677 W US 9302677W WO 9320123 A1 WO9320123 A1 WO 9320123A1
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WO
WIPO (PCT)
Prior art keywords
polymer
adhesive material
polyfunctional
substrates
epoxies
Prior art date
Application number
PCT/US1993/002677
Other languages
French (fr)
Inventor
Thomas F. Gardeski
Diane G. Novak
Original Assignee
Courtaulds Performance Films
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 Courtaulds Performance Films filed Critical Courtaulds Performance Films
Priority to EP93909150A priority Critical patent/EP0635035A4/en
Priority to CA002133839A priority patent/CA2133839A1/en
Priority to JP5517523A priority patent/JPH07509010A/en
Publication of WO1993020123A1 publication Critical patent/WO1993020123A1/en

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J163/00—Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
    • C08G18/4045—Mixtures of compounds of group C08G18/58 with other macromolecular compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/83—Chemically modified polymers
    • C08G18/831—Chemically modified polymers by oxygen-containing compounds inclusive of carbonic acid halogenides, carboxylic acid halogenides and epoxy halides
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
    • C08L75/04—Polyurethanes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
    • C09J175/04—Polyurethanes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
    • C09J175/04—Polyurethanes
    • C09J175/06—Polyurethanes from polyesters
    • H—ELECTRICITY
    • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K3/00—Apparatus or processes for manufacturing printed circuits
    • H05K3/38—Improvement of the adhesion between the insulating substrate and the metal
    • H05K3/386—Improvement of the adhesion between the insulating substrate and the metal by the use of an organic polymeric bonding layer, e.g. adhesive

Definitions

  • This invention is directed to three-dimensional polymeric adhesive materials and methods for producing such materials.
  • One aspect of the present invention is a process for producing a three-dimensional polymeric adhesive material.
  • the process comprises:
  • the starting polymer can contain an active hydrogen and have a maximum acid value of 2.
  • Such a starting polymer can be selected from the group
  • the starting polymer is a high molecular weight
  • the starting polymer can be a polyfunctional hydroxy-containing polymer having a hydroxy number of at least 10.
  • the starting polymer can be a polyfunctional hydroxy-containing polymer having a hydroxy number of at least 10.
  • polyfunctional hydroxy-containing polymer is selected from the group consisting of polyols, polyesters,
  • polyurethanes and mixtures thereof.
  • the polyfunctional nucleophile is a polyfunctional nitrogen-containing compound. More preferably, the polyfunctional nitrogen-containing compound is selected from the group consisting of
  • the polyelectrophile comprises at least one polyepoxide. More preferably, the polyepoxide is selected from the group consisting of bisphenol A-epichlorohydrin epoxies, novolac epoxies, and mixtures thereof. Most preferably, the polyexpoxide comprises a mixture of bisphenol A-epichlorohydrin epoxies and novolac epoxies.
  • the step of reacting the adduct product with the at least one polyepoxide comprises heating a mixture of the adduct product and the at least one polyepoxide to a temperature between about 250°F and about 400°F.
  • the high molecular weight polyester comprises from about 50% to about 90% by weight of the three-dimensional polymeric adhesive material and the polyepoxide comprises from about 10% to about 50% by weight of the three-dimensional polymeric adhesive material.
  • Another aspect of the present invention is a process for bonding at least two substrates. The process comprises the steps of:
  • the substrates are selected from the group consisting of film substrates, foil substrates, and hardboard substrates.
  • the adhesive comprises:
  • each cross-link comprising a polymer linked to the nitrogen atoms of the polymer moieties through reaction of an electrophile with the nitrogen atoms.
  • the linear polymer moieties are selected from the group consisting of polycarboxylic acids, polyesters, polyamides, polyacrylics,
  • the linear polymer moieties are formed by reaction of a hydroxy-containing polymer with a polyfunctional nitrogen-containing nucleophile.
  • the polyfunctional nitrogen-containing nucleophile is selected from the group
  • One preferred version of the three-dimensional polymeric adhesive of the present invention comprises:
  • the cross-links preferably comprise at least one polyepoxide selected from the group consisting of bisphenol A-epichlorohydrin epoxies, novolac epoxies, and mixtures thereof.
  • the polyepoxide comprises a mixture of bisphenol A-epichlorohydrin epoxies having the formula
  • n is an integer from 1 to about 20, n being independently chosen for the bisphenol A-epichlorohydrin epoxies and for the novolac epoxies.
  • a composite structure formed according to the invention comprises:
  • adhesive material comprising:
  • cross-links between the nitrogens of the polymer moieties each cross-link comprising a polymer linked to the nitrogen atoms of the polymer moieties through reaction of an electrophile with the nitrogen atoms.
  • One aspect of the present invention is a process for producing a three-dimensional polymeric adhesive material.
  • the polymeric adhesive material produced by this process has improved peel strength, chemical resistance, moisture resistance, high
  • this process comprises:
  • the starting polymer can contain an active hydrogen, with a maximum acid value of 2.
  • Such polymers can be polycarboxylic acids, polyesters, polyamides, polyacrylics, polyfunctional phenolic resins, or mixtures thereof.
  • the starting polymer can be a polyfunctional hydroxy-containing polymer having a hydroxy number of at least 10.
  • the polyfunctional hydroxy-containing polymer can be a polyol, a polyester, a polyurethane, or a mixture thereof.
  • the starting polymer is a high molecular weight polyester with hydroxyl end-group functionality of the alcohol type.
  • the polyfunctional nucleophile can be a
  • polyfunctional nitrogen-containing compound include polyamines, polyaziridines, and
  • polystyrene foam preferably, polystyrene foam, polystyrene foam, and mixtures thereof.
  • the polyfunctional nitrogen-containing compound is a polystyrene foam, polystyrene foam, and mixtures thereof.
  • the polyfunctional nitrogen-containing compound is a polystyrene foam, polystyrene foam, and mixtures thereof.
  • a particularly suitable starting polymer is a polyester resin such as DuPont 49002 base.
  • starting polymer and/or aryl moieties within the starting polymer or polyfunctional nucleophile can be optionally substituted with methyl and/or C 2 -C 5 alkyl.
  • starting polymer and “polyfunctional nucleophile”, as used herein, include compounds
  • reaction of the starting polymer with the polyfunctional nucleophile takes place slowly at room temperature and takes place more rapidly at about 250°F. Typically, this reaction is performed in a solvent, such as a 90%:10% mixture of methylene chloride: cyclohexanone.
  • the second stage of the process comprised is reacting the adduct product with a polyelectrophile to generate the three-dimensional polymeric adhesive
  • the polyelectrophile is preferably a
  • polyepoxide More preferably, it is a polyepoxide selected from the group consisting of bisphenol A-epichlorohydrin epoxies, novolac epoxies, or a mixture thereof. Most preferably, the polyelectrophile is a mixture of ⁇ bisphenol A-epichlorohydrin epoxy, such as Celanese Epi-Rez-51 32, and a novolac epoxy, such as Dow DEN 438.
  • the bisphenol A-epichlorohydrin epoxy has the following structure:
  • n is an integer from 1 to about 20.
  • the novolac epoxy has the following structure:
  • n is an integer from 1 to about 20.
  • the values of n are independently chosen for the bis-epi and novolac epoxies.
  • the high molecular weight polyester and at least one polyepoxide are used to form the three-dimensional polymeric material, the high
  • molecular weight polyester comprises from about 50% to about 90% by weight of the three-dimensional polymeric adhesive material and the polyepoxide comprises from about 10% to about 50% by weight of the three-dimensional polymeric adhesive material.
  • the reaction of the adduct product and the polyelectrophile preferably takes place at a temperature from about 250oF to about 400oF.
  • the first and second stage reactions are depicted below:
  • R represents the ester repeat unit and x represents the number of ester repeat units and n represents the number of organic aromatic
  • the pressure at which the reaction occurs is generally not critical.
  • the reaction typically takes place at atmospheric pressure.
  • the reaction typically occurs in an aprotic, moderately polar solvent or a mixture of such solvents.
  • exemplary solvents are a mixture of methylene chloride and cyclohexanone or methyl ethyl ketone, or a mixture of methylene chloride and cyclohexanone together with methyl ethyl ketone.
  • suitable solvents are not to be limited to these combinations; the choice of solvent is generally not critical. II.
  • the process of producing the adhesive of the present invention can be incorporated into a process for bonding at least two substrates.
  • this bonding process comprises of the steps of:
  • the substrates used for this procedure can be film substrates, foil substrates, or hardboard
  • a typical example of a film substrate is polyimide film.
  • the substrates can be of the same materials or different materials.
  • the substrates can be electronic circuit boards or other electronic structural components.
  • Another aspect of the invention is an improved three-dimensional polymeric adhesive material comprising:
  • the adhesive comprises:
  • this adhesive material can be formed in situ for bonding at least two substrates.
  • the substrates can be film substrates, foil substrates, or hardboard substrates.
  • a composite material can be formed.
  • the composite material can be formed.
  • substrates is bonded to at least one other substrate by the adhesive material.
  • the invention is illustrated by the following example. The example is for illustrative purposes and is not to be construed as limiting the scope of the
  • An example of the adhesive material of the present invention includes the following components:
  • a polyester resin having a solids content of 17-20% comprised of Dupont 49002 base in a solvent mixture of 90%: 10% (w/w) methylene chloride:
  • the adhesive coating composition is made by adding 80% by solids of the polyester component, 10% by solids of the epoxy novolac, 10% by solids of the bis-epi epoxy, and 1.2 parts by weight of the isocyanate in an open container without agitation. The composition is then agitated well for 1 to 5 minutes. The container is then capped with an airtight lid for 30 minutes to allow for the onset of the isocyanate/polyester reaction.
  • polyester and isocyanate are combined, thoroughly mixed, and then allowed to stand at room temperature for a minimum of 30 minutes prior to the epoxy addition to allow onset of the isocyanate/polyester reaction.
  • the adhesive coating composition is then applied by means of the reverse roll coating technique to a 1 mil polyimide film to yield a 1 mil dry coat weight. Drying (i.e., removal of the solvents) is accomplished through a 75-foot, 3-zone oven at 212°F and 25 feet per minute.
  • the coated substrate is then positioned next to the treated side of a 1 ounce copper foil, where the copper foil surface is treated with Oak CMC-111 compound to enhance bondability.
  • the polyimide film and copper foil are heated to a temperature of 225°F to 400°F with an applied pressure of 80 psi (pounds/square inch) to 120 psi through a coater/laminator combining station as part of a continuous operation.
  • the resulting roll is brought onto a six inch core, left at room temperature for 1 to 7 days, then post cured as follows: 2 hours at 150°F, 2 hours at 275°F, and 2 hours at 350°F.
  • a composite structure was prepared according to the first of the above procedures. The resulting composite structure was prepared according to the first of the above procedures. The resulting composite structure was prepared according to the first of the above procedures. The resulting composite structure was prepared according to the first of the above procedures. The resulting composite structure was prepared according to the first of the above procedures. The resulting composite structure was prepared according to the first of the above procedures. The resulting composite structure was prepared according to the first of the above procedures. The resulting
  • the present invention provides an adhesive system with extremely balanced properties and the added benefit of superior Z-axis stability through a unique curing mechanism. More specifically, the present invention provides an epoxy-based laminating adhesive that can be continuously processed and cured without the evolution of byproducts to provide a flexible bond-ply with superior overall properties, including excellent Z-axis stability.
  • the adhesive material is applicable to film substrates such as polyimide, foil substrates such as copper, and hardboard substrates, such as FR4
  • the adhesive of the present invention also possesses superior peel strength, chemical resistance, moisture resistance, and temperature stability. It is particularly suitable for use in the bonding of electronic construction materials, such as those intended for use in severe environmental
  • the adhesive of the present invention is suitable for use in under-the-hood

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Laminated Bodies (AREA)

Abstract

A process for producing an improved three-dimensional polymeric adhesive material comprises: (1) reacting a starting polymer containing an active hydrogen or hydroxy function with a polyfunctional nucleophile to form an adduct product; and (2) reacting the adduct product with a polyelectrophile to generate a three-dimensional polymeric adhesive material. Preferably, the starting polymer is a high molecular weight polyester, the polyfunctional nucleophile is a polyisocyanate, and the polyelectrophile is at least one polyepoxide. The present invention also encompasses processes for bonding at least two substrates by generating the adhesive material between them, as well as the adhesive material itself. The invention is particularly suitable for bonding electronic components such as printed circuit boards.

Description

A HIGH PERFORMANCE EPOXY BASED LAMINATING ADHESIVE
CROSS-REFERENCES
This application is a continuation-in-part of Application Serial No. 07/483,266, by Thomas F. Gardeski and Diane G. Novak, filed February 15, 1990, which is, in turn, a continuation of Application Serial No.
07/153,141, by Thomas F. Gardeski and Diane G. Novak, filed February 8, 1988, and now abandoned, both of which are also entitled "A High Performance Epoxy Based
Laminating Adhesive." These two applications are hereby incorporated in their entirety by this reference.
BACKGROUND OF THE INVENTION
This invention is directed to three-dimensional polymeric adhesive materials and methods for producing such materials.
During the past quarter century, the rapid growth of the electronic circuits industry has resulted in the development of higher performance construction materials. However, the development of high performance adhesive materials and systems to bond the construction materials together has not kept pace. This lack of higher performance adhesive materials is particularly felt in the assembly of electronic components for use in severe environmental conditions, such as under-the-hood automotive and military applications. Adhesive materials and systems that are currently available meet some of the requirements for such properties as peel strength, chemical resistance, moisture resistance, high
temperature stability, dimensional stability, especially in the Z-axis direction, and ease of processing.
However, these materials and systems typically fail to meet one or more of these requirements. Therefore, a need exists for an adhesive material that meets all of the requirements for use under severe environmental conditions while retaining ease of application. SUMMARY
We have developed a three-dimensional adhesive material and a process for preparing it that meets these needs and provides an improved adhesive for use under severe environmental conditions, particularly in the assembly of electronic components.
One aspect of the present invention is a process for producing a three-dimensional polymeric adhesive material. The process comprises:
(1) reacting a starting polymer containing an active hydrogen or hydroxy function with a polyfunctional nucleophile to form an adduct product; and (2) reacting the adduct product with a
polyelectrophile to generate a three-dimensional
polymeric adhesive material. The starting polymer can contain an active hydrogen and have a maximum acid value of 2. Such a starting polymer can be selected from the group
consisting of polycarboxylic acids, polyesters,
polyamides, polyacrylics, polyfunctional phenolic resins, and mixtures thereof. Preferably, in this alternative, the starting polymer is a high molecular weight
polyester.
Alternatively, the starting polymer can be a polyfunctional hydroxy-containing polymer having a hydroxy number of at least 10. Preferably, the
polyfunctional hydroxy-containing polymer is selected from the group consisting of polyols, polyesters,
polyurethanes, and mixtures thereof.
Preferably, the polyfunctional nucleophile is a polyfunctional nitrogen-containing compound. More preferably, the polyfunctional nitrogen-containing compound is selected from the group consisting of
polyamines, polyaziridines, polyisocyanates, and mixtures thereof. Most preferably, the polyfunctional nitrogen-containing compound is a polyisocyanate. Preferably, the polyelectrophile comprises at least one polyepoxide. More preferably, the polyepoxide is selected from the group consisting of bisphenol A-epichlorohydrin epoxies, novolac epoxies, and mixtures thereof. Most preferably, the polyexpoxide comprises a mixture of bisphenol A-epichlorohydrin epoxies and novolac epoxies.
Preferably, when the polyelectrophile comprises at least one polyepoxide, the step of reacting the adduct product with the at least one polyepoxide comprises heating a mixture of the adduct product and the at least one polyepoxide to a temperature between about 250°F and about 400°F.
Preferably, when a high molecular weight polyester and at least one polyepoxide are used to form the three-dimensional polymeric material, the high molecular weight polyester comprises from about 50% to about 90% by weight of the three-dimensional polymeric adhesive material and the polyepoxide comprises from about 10% to about 50% by weight of the three-dimensional polymeric adhesive material. Another aspect of the present invention is a process for bonding at least two substrates. The process comprises the steps of:
(1) reacting a starting polymer containing an active hydrogen or hydroxy function with a polyfunctional nucleophile to form an adduct product;
(2) mixing the adduct product with a polyelectrophile to generate a bonding precursor;
(3) applying the bonding precursor between the substrates prior to the reaction between the adduct product and the polyelectrophile; and
(4) reacting the adduct product with the polyelectrophile to generate a three-dimensional polymer adhesive material between the substrates, thereby bonding the substrates.
Typically, the substrates are selected from the group consisting of film substrates, foil substrates, and hardboard substrates.
Another aspect of the present invention is a three-dimensional adhesive produced by the process described above. In general, the adhesive comprises:
(1) at least two linear polymer moieties, each moiety comprising a polymer containing nucleophilic nitrogen atoms capable of reaction with an electrophile; and
(2) cross-links between the nitrogens of the polymer moieties, each cross-link comprising a polymer linked to the nitrogen atoms of the polymer moieties through reaction of an electrophile with the nitrogen atoms. Preferably, the linear polymer moieties are selected from the group consisting of polycarboxylic acids, polyesters, polyamides, polyacrylics,
polyfunctional phenolic resins, and mixtures thereof.
Preferably, the linear polymer moieties are formed by reaction of a hydroxy-containing polymer with a polyfunctional nitrogen-containing nucleophile. Preferably, the polyfunctional nitrogen-containing nucleophile is selected from the group
consisting of polyamines, polyaziridines,
polyisocyanates, and mixtures thereof. One preferred version of the three-dimensional polymeric adhesive of the present invention comprises:
(1) at least two linear urethane linked polymer moieties, each moiety comprising a hydroxy-terminated polyester linked in urethane linkage by an aromatic isocyanate; and
(2) cross-links between the nitrogens of the urethane linked polymer moieties, each cross-link
comprising a phenyl-containing polymer linked to the nitrogen atoms of the urethane linkages by -CH2-CHOH-linkages, with the methylene groups of the linkages being bonded directly to the nitrogen atoms such that the cross-links form a three-dimensional polymeric structure. In this version, the cross-links preferably comprise at least one polyepoxide selected from the group consisting of bisphenol A-epichlorohydrin epoxies, novolac epoxies, and mixtures thereof.
More preferably, the polyepoxide comprises a mixture of bisphenol A-epichlorohydrin epoxies having the formula
Figure imgf000009_0001
and novolac epoxies having the formula
Figure imgf000009_0002
wherein n is an integer from 1 to about 20, n being independently chosen for the bisphenol A-epichlorohydrin epoxies and for the novolac epoxies.
The adhesive material of the present invention can be used to bond at least two substrates, thereby forming a composite structure. A composite structure formed according to the invention comprises:
(1 ) at least two bondable substrates; and
(2) a three-dimensional polymeric adhesive material in adhesive contact with each of the substrates such that each of the substrates is bonded to at least one other substrate by the adhesive material, the
adhesive material comprising:
(a) at least two linear polymer moieties, each moiety comprising a polymer containing nucleophilic nitrogen atoms capable of reaction with an electrophile; and
(b) cross-links between the nitrogens of the polymer moieties, each cross-link comprising a polymer linked to the nitrogen atoms of the polymer moieties through reaction of an electrophile with the nitrogen atoms.
DESCRIPTION I. The Adhesive Production Process
One aspect of the present invention is a process for producing a three-dimensional polymeric adhesive material. The polymeric adhesive material produced by this process has improved peel strength, chemical resistance, moisture resistance, high
temperature stability, and dimensional stability. It is easy to process and is particularly suitable for use with electronic construction materials, such as printed circuit boards. In general, this process comprises:
(1) reacting a starting polymer containing an active hydrogen function or hydroxy function with a polyfunctional nucleophile to form an adduct product; and (2) reacting the adduct product with a
polyelectrophile to generate a three-dimensional
polymeric adhesive material. The starting polymer can contain an active hydrogen, with a maximum acid value of 2. Such polymers can be polycarboxylic acids, polyesters, polyamides, polyacrylics, polyfunctional phenolic resins, or mixtures thereof.
Alternatively, the starting polymer can be a polyfunctional hydroxy-containing polymer having a hydroxy number of at least 10. The polyfunctional hydroxy-containing polymer can be a polyol, a polyester, a polyurethane, or a mixture thereof.
Preferably, the starting polymer is a high molecular weight polyester with hydroxyl end-group functionality of the alcohol type.
The polyfunctional nucleophile can be a
polyfunctional nitrogen-containing compound. Such compounds include polyamines, polyaziridines,
polyisocyanates, and mixtures thereof. Preferably, the polyfunctional nitrogen-containing compound is a
polyisocyanate.
A particularly suitable starting polymer is a polyester resin such as DuPont 49002 base. A
particularly suitable polyelectrophile is a
polyfunctional isocyanate sold by Mobay.Chemical Corp., Pittsburgh, Pennsylvania, under the name of Mondur MRS, which is a polymethylene polyphenylene ester of isocyanic acid.
Carbon atoms of alkyl and/or aryl moieties within the starting polymer or polyfunctional nucleophile can be optionally substituted with methyl and/or C2-C5 alkyl. The terms "starting polymer" and "polyfunctional nucleophile", as used herein, include compounds
optionally substituted with methyl and/or C2-C3 alkyl. The reaction of the starting polymer with the polyfunctional nucleophile takes place slowly at room temperature and takes place more rapidly at about 250°F. Typically, this reaction is performed in a solvent, such as a 90%:10% mixture of methylene chloride: cyclohexanone.
The second stage of the process comprised is reacting the adduct product with a polyelectrophile to generate the three-dimensional polymeric adhesive
material. The polyelectrophile is preferably a
polyepoxide. More preferably, it is a polyepoxide selected from the group consisting of bisphenol A-epichlorohydrin epoxies, novolac epoxies, or a mixture thereof. Most preferably, the polyelectrophile is a mixture of α bisphenol A-epichlorohydrin epoxy, such as Celanese Epi-Rez-51 32, and a novolac epoxy, such as Dow DEN 438. The bisphenol A-epichlorohydrin epoxy has the following structure:
Figure imgf000013_0001
wherein n is an integer from 1 to about 20. The novolac epoxy has the following structure:
Figure imgf000013_0002
wherein n is an integer from 1 to about 20. The values of n are independently chosen for the bis-epi and novolac epoxies.
Preferably, when a high molecular weight polyester and at least one polyepoxide are used to form the three-dimensional polymeric material, the high
molecular weight polyester comprises from about 50% to about 90% by weight of the three-dimensional polymeric adhesive material and the polyepoxide comprises from about 10% to about 50% by weight of the three-dimensional polymeric adhesive material. The reaction of the adduct product and the polyelectrophile preferably takes place at a temperature from about 250ºF to about 400ºF. The first and second stage reactions are depicted below:
Figure imgf000014_0001
where R represents the ester repeat unit and x represents the number of ester repeat units and n represents the number of organic aromatic
repeat units in the isocyanate component.
Figure imgf000014_0002
The pressure at which the reaction occurs is generally not critical. The reaction typically takes place at atmospheric pressure.
The reaction typically occurs in an aprotic, moderately polar solvent or a mixture of such solvents. Exemplary solvents are a mixture of methylene chloride and cyclohexanone or methyl ethyl ketone, or a mixture of methylene chloride and cyclohexanone together with methyl ethyl ketone. However, suitable solvents are not to be limited to these combinations; the choice of solvent is generally not critical. II. Use of the Adhesive for Bonding
The process of producing the adhesive of the present invention can be incorporated into a process for bonding at least two substrates. In general, this bonding process comprises of the steps of:
(1) reacting a starting polymer with a
polyfunctional nucleophile to form an adduct product, as described above;
(2) mixing the adduct product with a polyelectrophile to generate a bonding precursor;
(3) applying the bonding precursor between the substrates prior to a reaction between the adduct product and the polyelectrophile; and (4) reacting the adduct product with the polyelectrophile to generate a three-dimensional
polymeric adhesive material between the substrates, thereby bonding the substrates.
The substrates used for this procedure can be film substrates, foil substrates, or hardboard
substrates. A typical example of a film substrate is polyimide film. The substrates can be of the same materials or different materials. The substrates can be electronic circuit boards or other electronic structural components.
III. The Adhesive Compound
Another aspect of the invention is an improved three-dimensional polymeric adhesive material comprising:
(1) at least two linear polymer moieties, each moiety comprising a polymer containing nucleophilic nitrogen atoms capable of reaction with an electrophile; and
(2) cross-links between the nitrogens of the polymer moieties, each cross-link comprising a polymer linked to the nitrogen atoms of the polymer moieties through reaction of an electrophile with the nitrogen atoms. Preferably, the adhesive comprises:
(1) at least two linear urethane linked polymer moieties, each moiety comprising a hydroxy-terminated polyester linked in urethane linkage by an aromatic isocyanate; and
(2) cross-links between the nitrogen of the urethane linked polymer moieties, each cross-link
comprising a phenyl-containing polymer linked to the nitrogen atoms of the polyurethanes by -CH2-CHOH- linkages with the CH2 moieties being located adjacent to the nitrogen atoms.
As disclosed above, this adhesive material can be formed in situ for bonding at least two substrates. The substrates can be film substrates, foil substrates, or hardboard substrates.
When at least two or more substrates are bonded by the adhesive of the present invention, a composite material can be formed. The composite material
comprises:
(1) at least two bondable substrates; and
(2) the three-dimensional polymeric adhesive material of the present invention in adhesive contact with each of the substrates such that each of the
substrates is bonded to at least one other substrate by the adhesive material. The invention is illustrated by the following example. The example is for illustrative purposes and is not to be construed as limiting the scope of the
invention in any manner.
Example
An example of the adhesive material of the present invention includes the following components:
(1) a polyester resin having a solids content of 17-20% comprised of Dupont 49002 base in a solvent mixture of 90%: 10% (w/w) methylene chloride:
cyclohexanone;
(2) an epoxy novolac at 85% solids content composed of Dow DEN 438-EK85 in methyl ethyl ketone;
(3) a bis-epi epoxy composed of Celanese Epi-Rez 5132 at 100% solids content; and
(4) a polyfunctional isocyanate used as a curative component, Mondur MRS from Mobay Chemical Corp.
The components can be combined according to either of the following two procedures:
(1) The adhesive coating composition is made by adding 80% by solids of the polyester component, 10% by solids of the epoxy novolac, 10% by solids of the bis-epi epoxy, and 1.2 parts by weight of the isocyanate in an open container without agitation. The composition is then agitated well for 1 to 5 minutes. The container is then capped with an airtight lid for 30 minutes to allow for the onset of the isocyanate/polyester reaction.
(2) The polyester and isocyanate are combined, thoroughly mixed, and then allowed to stand at room temperature for a minimum of 30 minutes prior to the epoxy addition to allow onset of the isocyanate/polyester reaction.
The adhesive coating composition is then applied by means of the reverse roll coating technique to a 1 mil polyimide film to yield a 1 mil dry coat weight. Drying (i.e., removal of the solvents) is accomplished through a 75-foot, 3-zone oven at 212°F and 25 feet per minute. The coated substrate is then positioned next to the treated side of a 1 ounce copper foil, where the copper foil surface is treated with Oak CMC-111 compound to enhance bondability. The polyimide film and copper foil are heated to a temperature of 225°F to 400°F with an applied pressure of 80 psi (pounds/square inch) to 120 psi through a coater/laminator combining station as part of a continuous operation. The resulting roll is brought onto a six inch core, left at room temperature for 1 to 7 days, then post cured as follows: 2 hours at 150°F, 2 hours at 275°F, and 2 hours at 350°F.
A composite structure was prepared according to the first of the above procedures. The resulting
composite structure exhibited the properties shown in Table 1 when tested per ANSI/IPC-FC-232B and 241B procedures:
TABLE 1
PROPERTIES OF ADHESIVE COMPOSITE STRUCTURE
Initial Peel 20 plia Peel After Solder 21 pli Chemical Resistance:
Methyl Ethyl Ketone 21 pli
Toluene 20 pli
Isopropyl Alcohol 21 pli
Trichloroethylene/Methylene Chloride 21 pli Solder Float Pass
Aging (96 hours at NO Bond 275°F in air circulating oven) Strength Change
pli = pounds per linear inch
ADVANTAGES OF THE INVENTION
The present invention provides an adhesive system with extremely balanced properties and the added benefit of superior Z-axis stability through a unique curing mechanism. More specifically, the present invention provides an epoxy-based laminating adhesive that can be continuously processed and cured without the evolution of byproducts to provide a flexible bond-ply with superior overall properties, including excellent Z-axis stability. The adhesive material is applicable to film substrates such as polyimide, foil substrates such as copper, and hardboard substrates, such as FR4
(fiberglass impregnated hardboard). The adhesive of the present invention also possesses superior peel strength, chemical resistance, moisture resistance, and temperature stability. It is particularly suitable for use in the bonding of electronic construction materials, such as those intended for use in severe environmental
conditions. In particular, the adhesive of the present invention is suitable for use in under-the-hood
automotive and military applications.
Although the present invention has been
described in considerable detail with reference to certain preferred versions thereof, other versions are possible. Therefore the spirit and scope of the pending claims should not be limited to the description of the preferred versions contained herein.

Claims

We claim:
1. A process for producing a three-dimensional polymeric adhesive material comprising:
(a) reacting a starting polymer containing an active hydrogen or hydroxy function with a polyfunctional nucleophile to form an adduct product; and
(b) reacting the adduct product with a
polyelectrophile to generate a three-dimensional
polymeric adhesive material.
2. The process of claim 1 wherein the starting polymer contains an active hydrogen and has a maximum acid value of 2.
3. The process of claim 2 wherein the starting polymer is selected from the group consisting of
polycarboxylic acids,, polyesters, polyamides,
polyacrylics, polyfunctional phenolic resins, and
mixtures thereof.
4. The process of claim 3 wherein the starting polymer comprises a high molecular weight polyester.
5. The process of claim 1 wherein the starting polymer is a polyfunctional hydroxy-containing polymer having a hydroxy number of at least 10.
6. The process of claim 5 where the
polyfunctional hydroxy-containing polymer is selected from the group consisting of polyols, polyesters,
polyurethanes, and mixtures thereof.
7. The process of claim 6 where the polyfunctional hydroxy-containing polymer is a polyester.
8. The process of claim 1 wherein the polyfunctional nucleophile is a polyfunctional nitrogen-containing compound.
9. The process of claim 8 wherein the polyfunctional nitrogen-containing compound is selected from the group consisting of polyamines, polyaziridines, polyisocyanates, and mixtures thereof.
10. The process of claim 9 wherein the
polyfunctional nitrogen-containing compound is a
polyisocyanate.
11. The process of claim 1 wherein the
polyelectrophile comprises at least one polyepoxide.
12. The process of claim 11 wherein the polyepoxide is selected from the group consisting of bisphenol A-epichlorohydrin epoxies, novolac epoxies, and mixtures thereof.
13. The process of claim 12 wherein the polyexpoxide comprises a mixture of bisphenol A-epichlorohydrin epoxies and novolac epoxies.
14. A process for producing a three-dimensional polymeric adhesive material comprising:
(a) reacting a starting polymer comprising a high molecular weight polyester with a polyisocyanate to form an adduct product; and
(b) reacting the adduct product with at least one polyepoxide selected from the group consisting of bisphenol A-epichlorohydrin epoxies, novolac epoxies, and mixtures thereof, to generate a three-dimensional
polymeric adhesive material.
15. The process of claim 14 wherein the high molecular weight polyester comprises from about 50% to about 90% by weight of the three-dimensional polymeric adhesive material and the polyepoxide comprises from about 10% to about 50% by weight of the three-dimensional polymeric adhesive material.
16. The process of claim 14 wherein the polyepoxide comprises a mixture of bisphenol A-epichlorohydrin epoxies and novolac epoxies.
17. The process of claim 14 wherein the step of reacting the adduct product with the at least one polyepoxide comprises heating a mixture of the adduct product and the at least one polyepoxide to a temperature between about 250°F and about 400°F.
18. A process for bonding at least two
substrates comprising the steps of :
(a) reacting a starting polymer containing an active hydrogen or hydroxy function with a polyfunctional nucleophile to form an adduct product;
(b) mixing the adduct product with a polyelectrophile to generate a bonding precursor;
(c) applying the bonding precursor between the substrates prior to the reaction between the adduct product and the polyelectrophile; and
(d) reacting the adduct product with the polyelectrophile to generate a three-dimensional polymer adhesive material between the substrates, thereby bonding the substrates.
19. The process of claim 18 wherein the substrates are selected from the group consisting of film substrates, foil substrates, and hardboard substrates.
20. The process of claim 18 wherein the starting polymer is selected from the group consisting of polycarboxylic acids, polyesters, polyamides,
polyacrylics, polyfunctional phenolic resins, and
mixtures thereof.
21. The process of claim 20 wherein the starting polymer comprises a high molecular weight polyester.
22. The process of claim 18 wherein the polyfunctional nucleophile is a polyfunctional nitrogen-containing compound selected from the group consisting of polyamines, polyaziridines, polyisocyanates, and mixtures thereof.
23. The process of claim 22 wherein the polyfunctional nitrogen-containing compound is a
polyisocyanate.
24. The process of claim 18 wherein the polyelectrophile comprises at least one polyepoxide selected from the group consisting of bisphenol A-epichlorohydrin epoxies, novolac epoxies, and mixtures thereof.
25. The process of claim 24 wherein the polyepoxide comprises a mixture of bisphenol A
epichlorohydrin epoxies and novolac epoxies.
26. A three-dimensional polymeric adhesive material comprising:
(a) at least two linear urethane linked polymer moieties, each moiety comprising a hydroxy- terminated polyester linked in urethane linkage by an aromatic isocyanate; and
(b) cross-links between the nitrogens of the urethane linked polymer moieties, each cross-link comprising a phenyl-containing polymer linked to the nitrogen atoms of the polyurethanes by — CH2— CHOH— linkages, with the methylene groups of the linkages being bonded directly to the nitrogen atoms such that the cross-links form a three-dimensional polymeric structure.
27. The polymeric adhesive material of claim
26 wherein the cross-links comprise at least one polyepoxide selected from the group consisting of bisphenol A-epichlorohydrin epoxies, novolac epoxies, and mixtures thereof.
28. The polymeric adhesive material of claim
27 wherein the polyepoxide comprises a mixture of bisphenol A-epichlorohydrin epoxies having the formula
Figure imgf000027_0001
and novolac epoxies having the formula
Figure imgf000028_0001
wherein n is an integer from 1 to about 20, n being independently chosen for the bisphenol A-epichlorohydrin epoxies and for the novolac epoxies.
29. A three-dimensional polymeric adhesive material comprising:
(a) at least two linear polymer moieties, each moiety comprising a polymer containing nucleophilic
nitrogen atoms capable of reaction with an electrophile;
and
(b) cross-links between the nitrogens of the polymer moieties, each cross-link comprising a polymer linked to the nitrogen atoms of the polymer moieties through reaction of an electrophile with the nitrogen atoms.
30. The polymer adhesive material of claim 29 wherein the linear polymer moieties are selected from the group consisting of polycarboxylic acids, polyesters,
polyamides, polyacrylics, polyfunctional phenolic resins, and mixtures thereof.
31. The polymer adhesive material of claim 30 wherein the linear polymer moieties are formed by
reaction of a hydroxy-containing polymer with a
polyfunctional nitrogen-containing nucleophile.
32. The polymer adhesive material of claim 31 wherein the polyfunctional nitrogen-containing
nucleophile is selected from the group consisting of polyammes, polyaziridmes, polyisocyanates, and mixtures thereof.
33. A composite structure comprising:
(a) at least two bondable substrates; and
(b) a three-dimensional polymeric adhesive material in adhesive contact with each of the substrates such that each of the substrates is bonded to at least one other substrate by the adhesive material, the
adhesive material comprising:
(i) at least two linear polymer moieties, each moiety comprising a polymer containing nucleophilic nitrogen atoms capable of reaction with an electrophile; and
(ii) cross-links between the nitrogens of the polymer moieties, each cross-link comprising a polymer linked to the nitrogen atoms of the polymer moieties through reaction of an electrophile with the nitrogen atoms.
34. The composite material of claim 33 wherein the bondable substrates are selected from the group consisting of film substrates, foil substrates, and hardboard substrates.
PCT/US1993/002677 1992-04-06 1993-04-06 A high performance epoxy based laminating adhesive WO1993020123A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP93909150A EP0635035A4 (en) 1992-04-06 1993-04-06 A high performance epoxy based laminating adhesive.
CA002133839A CA2133839A1 (en) 1992-04-06 1993-04-06 A high performance epoxy based laminating adhesive
JP5517523A JPH07509010A (en) 1992-04-06 1993-04-06 High performance epoxy-based laminating adhesive

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US86298392A 1992-04-06 1992-04-06
US07/862,983 1992-04-06

Publications (1)

Publication Number Publication Date
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EP0911353A1 (en) * 1997-10-20 1999-04-28 Toyo Boseki Kabushiki Kaisha Adhesive resin composition and adhesive film

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DE1720492B1 (en) * 1966-08-04 1972-05-31 Dow Chemical Co METHOD OF MANUFACTURING MODIFIED EPOXY POLY ADDUCTS
DE3727847A1 (en) * 1987-08-20 1989-03-02 Fuller H B Co MELT ADHESIVE AND METHOD FOR ITS PRODUCTION AND PROCESSING
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CA2004130A1 (en) * 1989-11-29 1991-05-29 Thomas F. Gardeski High performance epoxy based laminating adhesive

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0911353A1 (en) * 1997-10-20 1999-04-28 Toyo Boseki Kabushiki Kaisha Adhesive resin composition and adhesive film
US6194523B1 (en) 1997-10-20 2001-02-27 Toyo Boseki Kabushiki Kaisha Adhesive resin composition and adhesive film

Also Published As

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CA2133839A1 (en) 1993-10-14
EP0635035A4 (en) 1996-03-13
JPH07509010A (en) 1995-10-05
EP0635035A1 (en) 1995-01-25

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