WO2020186571A1 - 一种树脂组合物、包含其的预浸料以及层压板和印制电路板 - Google Patents
一种树脂组合物、包含其的预浸料以及层压板和印制电路板 Download PDFInfo
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- C—CHEMISTRY; METALLURGY
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates 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
- C08G59/18—Macromolecules 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
- C08G59/40—Macromolecules 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
- C08G59/4007—Curing agents not provided for by the groups C08G59/42 - C08G59/66
- C08G59/4071—Curing agents not provided for by the groups C08G59/42 - C08G59/66 phosphorus containing compounds
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- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
- C08L63/04—Epoxynovolacs
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B15/00—Layered products comprising a layer of metal
- B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
- B32B15/092—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin comprising epoxy resins
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B32B15/00—Layered products comprising a layer of metal
- B32B15/20—Layered products comprising a layer of metal comprising aluminium or copper
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
- B32B27/20—Layered products comprising a layer of synthetic resin characterised by the use of special additives using fillers, pigments, thixotroping agents
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/38—Layered products comprising a layer of synthetic resin comprising epoxy resins
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- C08G59/00—Polycondensates 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
- C08G59/18—Macromolecules 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
- C08G59/40—Macromolecules 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
- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
- C08G59/4215—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof cycloaliphatic
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- C08G59/00—Polycondensates 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
- C08G59/18—Macromolecules 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
- C08G59/40—Macromolecules 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
- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
- C08G59/4223—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof aromatic
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/16—Dicarboxylic acids and dihydroxy compounds
- C08G63/18—Dicarboxylic acids and dihydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
- C08G63/181—Acids containing aromatic rings
- C08G63/183—Terephthalic acids
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/16—Dicarboxylic acids and dihydroxy compounds
- C08G63/18—Dicarboxylic acids and dihydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
- C08G63/199—Acids or hydroxy compounds containing cycloaliphatic rings
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
- C08G63/692—Polyesters containing atoms other than carbon, hydrogen and oxygen containing phosphorus
- C08G63/6924—Polyesters containing atoms other than carbon, hydrogen and oxygen containing phosphorus derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/6926—Dicarboxylic acids and dihydroxy compounds
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- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/24—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs
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- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/24—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs
- C08J5/241—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs using inorganic fibres
- C08J5/244—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs using inorganic fibres using glass fibres
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- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/24—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs
- C08J5/249—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs characterised by the additives used in the prepolymer mixture
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/013—Fillers, pigments or reinforcing additives
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- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0066—Flame-proofing or flame-retarding additives
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/527—Cyclic esters
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/04—Condensation polymers of aldehydes or ketones with phenols only
- C08L61/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
- C08L61/14—Modified phenol-aldehyde condensates
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- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
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- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
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- 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
- H05K1/00—Printed circuits
- H05K1/02—Details
- H05K1/03—Use of materials for the substrate
- H05K1/0313—Organic insulating material
- H05K1/0353—Organic insulating material consisting of two or more materials, e.g. two or more polymers, polymer + filler, + reinforcement
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- 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
- H05K1/00—Printed circuits
- H05K1/02—Details
- H05K1/03—Use of materials for the substrate
- H05K1/0313—Organic insulating material
- H05K1/0353—Organic insulating material consisting of two or more materials, e.g. two or more polymers, polymer + filler, + reinforcement
- H05K1/0373—Organic insulating material consisting of two or more materials, e.g. two or more polymers, polymer + filler, + reinforcement containing additives, e.g. fillers
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2457/00—Electrical equipment
- B32B2457/08—PCBs, i.e. printed circuit boards
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2363/00—Characterised by the use of epoxy resins; Derivatives of epoxy resins
- C08J2363/04—Epoxynovolacs
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08L2201/00—Properties
- C08L2201/02—Flame or fire retardant/resistant
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- C08L2201/00—Properties
- C08L2201/22—Halogen free composition
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/20—Applications use in electrical or conductive gadgets
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- 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
- H05K1/00—Printed circuits
- H05K1/02—Details
- H05K1/03—Use of materials for the substrate
- H05K1/0313—Organic insulating material
- H05K1/032—Organic insulating material consisting of one material
- H05K1/0326—Organic insulating material consisting of one material containing O
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- 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
- H05K1/00—Printed circuits
- H05K1/02—Details
- H05K1/03—Use of materials for the substrate
- H05K1/0313—Organic insulating material
- H05K1/0353—Organic insulating material consisting of two or more materials, e.g. two or more polymers, polymer + filler, + reinforcement
- H05K1/0366—Organic insulating material consisting of two or more materials, e.g. two or more polymers, polymer + filler, + reinforcement reinforced, e.g. by fibres, fabrics
Definitions
- the present disclosure belongs to the technical field of printed circuit boards, and in particular relates to a resin composition and a prepreg containing the same, as well as a laminate and a printed circuit board.
- Resin prepregs are often used as substrate materials in printed circuit boards.
- halogen flame retardants are usually used in resin compositions to achieve flame retardancy.
- halogen flame retardants burn, they not only emit large amounts of smoke and have an unpleasant smell, but also produce highly corrosive hydrogen halide gas and carcinogens such as dioxins and dibenzofurans. Therefore, there is a need to develop resin compositions for halogen-free flame-retardant printed circuit laminates.
- the present disclosure provides a resin composition, characterized in that the resin composition comprises:
- Halogen-free epoxy resin 100 parts by weight
- Active ester resin 11-37 parts by weight
- n 2-15 and Ac represents an acetyl group.
- the halogen-free epoxy resin is selected from the group consisting of: biphenol novolac epoxy resin, DCPD type novolac epoxy resin, alkylene novolac epoxy resin, bisphenol A type novolac epoxy resin , Bisphenol AP type epoxy resin, bisphenol TMC type epoxy resin, and their combinations.
- the active ester resin is a compound represented by formula (II),
- X represents a phenyl group or a naphthyl group
- j is 0 or 1
- k is 0 or 1
- n is 0.25-1.25.
- the number average molecular weight of the active ester resin is 800 or less.
- the amount of the active ester resin is 24-37 parts by weight.
- the amount of the compound represented by formula (I) is 40-53 parts by weight.
- the resin composition further comprises cyanate ester or its prepolymer.
- the cyanate ester may be a cyanate ester compound containing at least 2 cyanooxy groups in the molecule, such as bisphenol A cyanate ester, or a prepolymer thereof.
- the amount of the cyanate ester or its prepolymer is 10-20 parts by weight Copies.
- the resin composition further includes a curing accelerator.
- a curing accelerator based on 100 parts by weight of the total amount of the halogen-free epoxy resin, the active ester resin and the compound represented by formula (I), the amount of the curing accelerator is 0.05-1 parts by weight.
- the curing accelerator is selected from the group consisting of: 4-dimethylaminopyridine, 2-methylimidazole, 2-methyl-4-ethylimidazole or 2-phenylimidazole, isooctanoic acid Zinc, and their combinations.
- the resin composition further contains flame retardant salts.
- the flame retardant salt is a phosphate compound.
- the amount of the flame retardant salt is 50 parts by weight or less.
- the resin composition further includes a filler.
- the filler is an organic and/or inorganic filler.
- the amount of the filler is 100 parts by weight or less.
- the present disclosure provides a prepreg, which is obtained by impregnating or coating a reinforcing material with the resin composition described above and semi-curing it.
- the present disclosure provides a laminate including at least one prepreg as described above.
- the present disclosure provides a printed circuit board comprising at least one prepreg or laminate as described above.
- the purpose of the present disclosure is to provide a resin composition.
- the resin composition can be used to prepare prepregs, and then to prepare laminates and printed circuit boards.
- the prepregs, laminates and printed circuit boards manufactured by using the composition have low dielectric loss factor, good flame retardancy, and at the same time have high-layer adhesion and low CTE.
- the inventors of the present disclosure unexpectedly discovered that when the resin composition of the present disclosure is composed of a compound represented by formula (I), an active ester and an epoxy resin, the resulting product will have particularly excellent dielectric properties.
- the present disclosure provides a resin composition, which comprises:
- Halogen-free epoxy resin 100 parts by weight
- Active ester resin 11-37 parts by weight
- n 2-15 and Ac represents an acetyl group.
- epoxy resin is used as the basic material to provide the cured product with excellent curing crosslink density.
- the present disclosure selects halogen-free epoxy resin without halogen.
- the active ester resin is selected as the curing agent to effectively enhance the crosslinking and curing effect of the cured product.
- a specific compound represented by formula (I) is selected, which can play a role in improving the dielectric properties of the cured product.
- the above-mentioned resin composition is obtained by using the mutual coordination and mutual synergistic promotion effect between the above three essential components.
- the prepregs, laminates and printed circuit boards manufactured by using the resin composition have low dielectric loss factor, good flame retardancy, and at the same time have high-layer adhesion and low CTE.
- the halogen-free epoxy resin component is a halogen-free epoxy resin.
- the present disclosure does not specifically limit the type of halogen-free epoxy resin.
- the halogen-free epoxy resin is selected from the group consisting of: biphenol novolac epoxy resin, DCPD novolac epoxy resin, alkylene novolac epoxy resin, bisphenol A novolac epoxy resin, double Phenol AP type epoxy resin, bisphenol TMC type epoxy resin, and combinations thereof.
- the advantages of these halogen-free epoxy resins are their low thermal expansion coefficient and dielectric properties.
- Active ester resin refers to a compound containing more than one active ester group in the molecule.
- the amount of the active ester resin is 11-37 parts by weight, and may be, for example, 11 parts by weight, 15 parts by weight, 25 parts by weight, 30 parts by weight, or 37 parts by weight, preferably 24-37 parts by weight. Within this range, the advantage is a better dielectric loss factor.
- the active ester resin is a compound represented by formula (II),
- X represents a phenyl group or a naphthyl group
- j is 0 or 1
- k is 0 or 1
- n is 0.25-1.25.
- the rigid structure such as benzene ring, naphthalene ring, and cyclopentadiene imparts high heat resistance to the active ester.
- the regularity of its structure and the same reaction process with epoxy resin The generation of secondary hydroxyl groups gives it good electrical properties and low water absorption.
- the inventors of the present disclosure have further unexpectedly discovered that, in the resin composition of the present disclosure, when the number average molecular weight of the active ester is controlled below 800, the dielectric properties of the resin composition can be further improved.
- the number average molecular weight of the active ester resin is 800 or less.
- the dielectric properties are better. Without relying on any theory, this may be because the active ester resin with a number average molecular weight of less than 800 can provide better wettability for the resin composition, thereby providing better dielectric properties for laminates and printed circuit board products.
- the amount of the compound represented by formula (I) is 40-66 parts by weight, and may be, for example, 40 parts by weight, 50 parts by weight, 55 parts by weight, 60 parts by weight or 66 parts by weight, preferably 40-53 parts by weight. Within this range, the advantage is a better dielectric loss factor.
- the degree of polymerization n of the compound represented by formula (I) is 2-15, and n may be 3, 7, 11, or 15, for example.
- the compound represented by formula (I) is a polymer in which there will be some particularly large molecular weight components, and the large molecular weight components will affect the wettability of the resin composition in the epoxy resin and active ester resin system. It is the phenomenon that the substrate of laminate or printed circuit board has dry flowers or white streaks.
- the inventors of the present disclosure unexpectedly discovered that by using an active ester resin with a molecular weight of 800 or less in the system of the present disclosure, the adverse effect of the high molecular weight part of the compound represented by formula (I) on the wettability can be effectively balanced. Improve wettability and provide better dielectric properties.
- the number average molecular weight of the compound represented by formula (I) is about 1300 to 7800, respectively.
- the resin composition may further include a cyanate ester or a prepolymer thereof, which can increase the glass transition temperature of the composition, and at the same time realize N-P synergistic flame retardancy with the compound represented by formula (I), thereby improving flame retardant efficiency.
- a cyanate ester or a prepolymer thereof which can increase the glass transition temperature of the composition, and at the same time realize N-P synergistic flame retardancy with the compound represented by formula (I), thereby improving flame retardant efficiency.
- the cyanate ester may be a cyanate ester compound containing at least 2 cyanooxy groups in the molecule, such as bisphenol A cyanate ester, or a prepolymer thereof, which can better improve the composition Glass transition temperature.
- the amount of the cyanate ester or its prepolymer may be 10-20 parts by weight, for example 10 parts by weight, 12 parts by weight, 14 parts by weight, 16 parts by weight, 18 parts by weight, or 20 parts by weight.
- the resin composition further includes a curing accelerator, which cures the resin and accelerates the curing speed of the resin.
- a curing accelerator which cures the resin and accelerates the curing speed of the resin.
- the amount of the curing agent accelerator is 0.05 to 1 part by weight, for example, 0.08 part by weight , 0.1 parts by weight, 0.15 parts by weight, 0.2 parts by weight, 0.25 parts by weight, 0.3 parts by weight, 0.35 parts by weight, 0.4 parts by weight, 0.45 parts by weight, 0.5 parts by weight, 0.55 parts by weight, 0.60 parts by weight, 0.65 parts by weight, 0.7 parts by weight Parts, 0.75 parts by weight, 0.8 parts by weight, 0.85 parts by weight, 0.9 parts by weight, or 0.95 parts by weight.
- the curing accelerator is selected from the group consisting of 4-dimethylaminopyridine, 2-methylimidazole, 2-methyl-4-ethylimidazole or 2-phenylimidazole, zinc isooctanoate , And their combination.
- the resin composition may further include flame-retardant salts, such as phosphate compounds, but it is not limited thereto.
- flame-retardant salts such as phosphate compounds, but it is not limited thereto.
- Phosphate compounds include nitrogen-containing phosphate compounds.
- the amount of the flame retardant salt is 50 parts by weight or less, for example, 5 parts by weight , 10 parts by weight, 15 parts by weight, 20 parts by weight, 25 parts by weight, 30 parts by weight, 35 parts by weight, 40 parts by weight, 45 parts by weight or 50 parts by weight.
- the resin composition further contains fillers, the fillers being organic and/or inorganic fillers, which are mainly used to adjust some of the physical properties of the composition, such as reducing the coefficient of thermal expansion (CTE), reducing water absorption and improving thermal conductivity Rate etc.
- CTE coefficient of thermal expansion
- reducing water absorption and improving thermal conductivity Rate etc.
- the amount of the filler is 100 parts by weight or less, preferably 50 parts by weight or less based on the total amount of the halogen-free epoxy resin, the active ester resin and the compound represented by formula (I) being 100 parts by weight.
- the amount of the filler is, for example, 0.5 parts by weight, 1 part by weight, 5 parts by weight, 10 parts by weight, 15 parts by weight, 20 parts by weight, 25 parts by weight, 30 parts by weight, 35 parts by weight, 40 parts by weight, 45 parts by weight , 50 parts by weight, 55 parts by weight, 60 parts by weight, 65 parts by weight, 70 parts by weight, 75 parts by weight, 80 parts by weight, 85 parts by weight, 90 parts by weight or 95 parts by weight.
- the inorganic filler is selected from fused silica, crystalline silica, spherical silica, hollow silica, aluminum hydroxide, alumina, talc, aluminum nitride, boron nitride, carbonized Any one or a mixture of at least two of silicon, barium sulfate, barium titanate, strontium titanate, calcium carbonate, calcium silicate, mica or glass fiber powder.
- the mixture is for example a mixture of fused silica and crystalline silica, a mixture of spherical silica and hollow silica, a mixture of aluminum hydroxide and aluminum oxide, a mixture of talc and aluminum nitride, and nitriding
- the organic filler is selected from any one or a mixture of at least two of polytetrafluoroethylene powder, polyphenylene sulfide or polyethersulfone powder.
- the mixture for example, a mixture of polytetrafluoroethylene powder and polyphenylene sulfide, a mixture of polyethersulfone powder and polytetrafluoroethylene powder, a mixture of polyphenylene sulfide and polyethersulfone powder, polytetrafluoroethylene powder, polyphenylene Mixture of sulfide and polyethersulfone powder.
- the filler is silica, and the median particle size of the filler is 1-15 ⁇ m, preferably the median particle size of the filler is 1-10 ⁇ m.
- the “comprising” mentioned in the present disclosure means that in addition to the aforementioned components, it can also contain other components, and these other components impart different characteristics to the resin composition.
- the “comprising” mentioned in the present disclosure can also be replaced with a closed “being” or “consisting of”.
- the resin composition may further contain various additives, and specific examples include antioxidants, heat stabilizers, antistatic agents, ultraviolet absorbers, pigments, colorants, lubricants, and the like. These various additives can be used alone, or two or more of them can be mixed and used.
- the conventional production method of the resin composition of the present disclosure take a container, put the solid components in first, then add the liquid solvent, stir until completely dissolved, add the liquid resin, filler, flame retardant and curing accelerator, continue stirring Even if it is uniform, finally adjust the liquid solid content to 60%-80% with a solvent to make a glue liquid.
- the second objective of the present disclosure is to provide a prepreg comprising a reinforcing material and the resin composition as described above attached to it after being dried by impregnation.
- Exemplary reinforcing materials are non-woven fabrics and/or other fabrics, such as natural fibers, organic synthetic fibers, and inorganic fibers.
- the glue is used to impregnate reinforcing materials such as glass cloth and other fabrics or organic fabrics, and the impregnated reinforcing materials are heated and dried in an oven at 155-170°C for 5-10 minutes to obtain a prepreg.
- the third object of the present disclosure is to provide a laminate comprising at least one prepreg as described above.
- the fourth objective of the present disclosure is to provide a printed circuit board comprising at least one prepreg or laminate as described above.
- the prepregs, laminates and printed circuit boards made of the resin composition of the present disclosure have low dielectric loss factor, good flame retardancy, and at the same time have high-layer adhesion and low CTE.
- the metal-clad laminate made from the above-mentioned resin composition was tested for its interlayer adhesion, CTE, and dielectric loss factor.
- the following examples are added to the detailed description and description, where the mass of the organic resin Calculated in parts by mass of organic solids.
- NC-3000H Biphenol novolac epoxy resin (obtained from Nippon Kayaku).
- HPC-7200HHH DCPD type phenolic epoxy resin (obtained from Japan DIC).
- HPC-8000-65T Active ester resin, a compound represented by formula (II), with a number average molecular weight of 800 or more (obtained from Japan DIC).
- HPC-8000L-65MT Active ester resin, a compound represented by formula (II), with a number average molecular weight of 800 or less (obtained from Japan DIC).
- E15-152T A compound represented by formula (I) (derived from ICL), where n is about 3.0.
- Phosphorus-containing compound 1 Reactive phosphorus-containing flame retardant, prepared with reference to Preparation Example 1 in CN108976705A.
- Phosphorus-containing compound 2 Reactive phosphorus-containing flame retardant, prepared with reference to Preparation Example 2 in CN108976705A.
- Phosphorus-containing compound 3 Phosphorus-containing phenolic resin, refer to the preparation example in CN105778413A.
- CE01PS Bisphenol A cyanate ester (obtained from Yangzhou Tianqi Chemical).
- FB-3Y Silica filler (from DENKA).
- BYK-W903 Filler dispersant (obtained from BYK).
- DMAP curing accelerator, 4-dimethylaminopyridine (obtained from Guangrong Chemical).
- Zinc isooctanoate curing accelerator (from Alfa Aesar).
- Interlayer adhesion axe-blade separation method: Use a knife to peel off one end of the copper clad laminate sample (width of 3mm, length of 150mm) with two layers of adhesive sheet about 20mm, and clamp the sample in the test On the clamp, the upper and lower ends are fixed to keep the sample in a vertical state. Peel one end of the test strip across the blade of the axe-shaped test head, and keep the separated surface of the sample on the same axis as the blade of the axe, start the peel strength tester, and apply a tensile force in the vertical direction at a speed of 50mm/min. Separate the sample with the edge at least 50mm, and the interlayer adhesion is the average separation force of the sample/the width of the sample.
- CTE Coefficient of Thermal Expansion
- Dielectric loss factor Test according to the method specified in IEC 61189-2-721 (SPDR), and the test frequency is 10GHz.
- Subsurface appearance of the substrate Use the standard method specified in IPC-TM-650 to test and judge whether there are any defects such as dry flowers and white lines in the substrate by visual inspection or slicing method.
- Comparative Examples 1-4 a different phosphorus-containing compound was used as a flame retardant instead of the compound represented by formula (I).
- the results show that the dielectric loss factor of the product is above 0.0083, which are all higher than those of Examples 1-7.
- Comparative Example 6 in which only the compound represented by the formula (I) and the epoxy resin were used but did not contain the active ester component, the dielectric loss of the product was 0.0081, and more white streaks were distributed therein.
- the results show that the active ester and the compound represented by formula (I) have a synergistic effect, and can obtain good interlayer adhesion while obtaining excellent dielectric properties.
- Example 7 the performance difference between Example 7 and Example 2 is similar, but there are a few white streaks in the substrate plate, and Df is increased, indicating that adjusting the number average molecular weight of the active ester resin has an effect on the resin composition.
- Wetting and dielectric properties can be further optimized. From the comparison of Examples 2 and 7, it can be seen that the number average molecular weight of the active ester will affect the dielectric properties of the product. In addition, it can be seen from the comparison of Comparative Examples 3 and 4 that when combined with other phosphorus-containing compound flame retardants, there is no correlation that the lower the number average molecular weight of the active ester resin, the better the dielectric properties of the product.
- the halogen-free circuit substrates of the present disclosure have prepregs, laminates and printed circuit boards made of the resin composition, which have low dielectric loss factors and good flame retardancy. , It also has high-layer adhesion and low CTE.
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Abstract
Description
Claims (11)
- 根据权利要求1所述的树脂组合物,其特征在于,所述无卤环氧树脂选自由以下各项组成的组:联苯酚醛环氧树脂、DCPD型酚醛环氧树脂、亚烷基酚醛环氧树脂、双酚A型酚醛环氧树脂、双酚AP型环氧树脂、双酚TMC型环氧树脂、和它们的组合。
- 根据权利要求1所述的树脂组合物,其特征在于,所述活性酯树脂的数均分子量为800以下。
- 根据权利要求1所述的树脂组合物,其特征在于,所述树脂组合物还包含氰酸酯或及其预聚物。
- 如权利要求1所述的树脂组合物,其特征在于,所述树脂组合物还包含固化促进剂。
- 如权利要求1所述的树脂组合物,其特征在于,所述树脂组合物还包含阻燃性盐类。
- 如权利要求1所述的树脂组合物,其特征在于,所述树脂组合物还包含填料。
- 一种预浸料,所述预浸料是通过对增强材料浸渍或涂布根据权利要求1所述的树脂组合物并将其半固化得到的。
- 一种层压板,所述层压板包含至少一张如权利要求9所述的预浸料。
- 一种印制电路板,所述印制电路板包含:至少一张如权利要求9所述的预浸料,或至少一张如权利要求10所述的层压板。
Priority Applications (4)
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JP2021556577A JP2022526307A (ja) | 2019-03-18 | 2019-04-08 | 樹脂組成物、ならびにそれを含むプリプレグ、積層板および印刷回路基板 |
EP19919811.0A EP3943549B1 (en) | 2019-03-18 | 2019-04-08 | Resin composition, prepreg containing same, laminate, and printed circuit board |
KR1020217028464A KR102600500B1 (ko) | 2019-03-18 | 2019-04-08 | 수지 조성물 및 이를 포함한 프리프레그, 적층판 및 인쇄회로기판 |
US17/437,555 US20220153989A1 (en) | 2019-03-18 | 2019-04-08 | Resin composition, prepreg containing same, laminate, and printed circuit board |
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CN201910206965.9 | 2019-03-18 | ||
CN201910206965.9A CN109929222B (zh) | 2019-03-18 | 2019-03-18 | 一种树脂组合物、包含其的预浸料以及层压板和印制电路板 |
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EP (1) | EP3943549B1 (zh) |
JP (1) | JP2022526307A (zh) |
KR (1) | KR102600500B1 (zh) |
CN (1) | CN109929222B (zh) |
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WO (1) | WO2020186571A1 (zh) |
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CN105778413A (zh) | 2014-12-26 | 2016-07-20 | 广东生益科技股份有限公司 | 一种无卤环氧树脂组合物以及使用它的预浸料和层压板 |
CN108976705A (zh) | 2017-06-05 | 2018-12-11 | 广东生益科技股份有限公司 | 一种无卤环氧树脂组合物以及使用它的预浸料和层压板 |
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TWI721024B (zh) * | 2015-11-13 | 2021-03-11 | 美商Icl Ip美國股份有限公司 | 用於熱固性樹脂之活性酯類固化劑化合物、包含彼之阻燃劑組成物、及由其所製成之物件 |
TWI808064B (zh) * | 2016-11-30 | 2023-07-11 | 美商Icl-Ip美國股份有限公司 | 熱固性樹脂之活性酯硬化劑、含彼之阻燃組成物及由彼製成的物品 |
TWI626664B (zh) * | 2017-02-07 | 2018-06-11 | 聯茂電子股份有限公司 | 具有低介電損耗的無鹵素環氧樹脂組成物 |
CN108219371B (zh) * | 2017-12-29 | 2020-08-18 | 广东生益科技股份有限公司 | 环氧树脂组合物、预浸料、层压板和印刷电路板 |
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2019
- 2019-03-18 CN CN201910206965.9A patent/CN109929222B/zh active Active
- 2019-04-08 EP EP19919811.0A patent/EP3943549B1/en active Active
- 2019-04-08 WO PCT/CN2019/081741 patent/WO2020186571A1/zh unknown
- 2019-04-08 KR KR1020217028464A patent/KR102600500B1/ko active IP Right Grant
- 2019-04-08 JP JP2021556577A patent/JP2022526307A/ja active Pending
- 2019-04-08 US US17/437,555 patent/US20220153989A1/en active Pending
- 2019-06-11 TW TW108120096A patent/TWI706980B/zh active
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CN103351578A (zh) * | 2013-07-19 | 2013-10-16 | 广东生益科技股份有限公司 | 一种用于形成天线用的介质基板的介质层的树脂组合物及其用途 |
CN103965587A (zh) * | 2014-05-28 | 2014-08-06 | 苏州生益科技有限公司 | 一种无卤树脂组合物及使用其制作的半固化片及层压板 |
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JP2022526307A (ja) | 2022-05-24 |
KR102600500B1 (ko) | 2023-11-09 |
EP3943549B1 (en) | 2023-09-06 |
TWI706980B (zh) | 2020-10-11 |
EP3943549C0 (en) | 2023-09-06 |
EP3943549A4 (en) | 2022-10-05 |
CN109929222B (zh) | 2021-07-30 |
TW201936748A (zh) | 2019-09-16 |
EP3943549A1 (en) | 2022-01-26 |
US20220153989A1 (en) | 2022-05-19 |
CN109929222A (zh) | 2019-06-25 |
KR20210125054A (ko) | 2021-10-15 |
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