CN106146843A - A kind of BDAPP type siliceous epoxy acid imide matrix resin and preparation method thereof - Google Patents
A kind of BDAPP type siliceous epoxy acid imide matrix resin and preparation method thereof Download PDFInfo
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- CN106146843A CN106146843A CN201610613872.4A CN201610613872A CN106146843A CN 106146843 A CN106146843 A CN 106146843A CN 201610613872 A CN201610613872 A CN 201610613872A CN 106146843 A CN106146843 A CN 106146843A
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- 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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C08G73/12—Unsaturated polyimide precursors
- C08G73/125—Unsaturated polyimide precursors the unsaturated precursors containing atoms other than carbon, hydrogen, oxygen or nitrogen in the main chain
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Abstract
The present invention relates to a kind of BDAPP type siliceous epoxy acid imide matrix resin and preparation method thereof, this matrix resin is by 2,2 pairs of [4 (2, the 4 diamino phenoxy) phenyl] propane (BDAPP), epoxy resin, 3 aminopropyltrialkoxysilane, imide oligomer thing and firming agent composition.Preparation method comprises the steps: that (1) prepares imide oligomer thing;(2) by 2,2 pairs [4 (2,4 diamino phenoxies) phenyl] propane (BDAPP), epoxy resin puts in reactor, after stirring hybrid reaction, add imide oligomer thing and continue stirring reaction, it is subsequently added 3 aminopropyltrialkoxysilane stirring reactions, adds firming agent and be uniformly mixed,.The composite can be widely applied to the bonding between the base material such as the metals such as steel, copper, aluminum and pottery, glass, polymer matrix composites, and the preparation of glass fibre, aramid fiber, carbon fibre reinforced composite, there is good industrialization prospect.
Description
Technical field
The invention belongs to macromolecule matrix resin and preparation field thereof, sub-particularly to a kind of BDAPP type siliceous epoxy acyl
Amine matrix resin and preparation method thereof.
Background technology
It is known that epoxy resin has many excellent performances: the adhesive property that (1) is good: adhesive strength is high, bonding
Wide, it and many metals (such as ferrum, steel, copper, aluminum, metal alloy etc.) or nonmetallic materials are (such as glass, pottery, resin base again
Condensation material, timber, plastics etc.) adhesive strength the highest, have even more than by the intensity of viscous material itself, therefore can be used for
In many stress members, it it is one of the main component of structural adhesive;(2) good processing characteristics: Formulaion of epoxy resin
The multiformity of motility, processing technique and product properties be the most prominent in macromolecular material;(3) good stability
Can: the solidification of epoxy resin mainly relies on the ring opening polyaddition of epoxy radicals, does not therefore produce low-molecular material in solidification process,
Its cure shrinkage is one of kind minimum in thermosetting resin, generally 1%-2%, if selecting suitable filler to make
Shrinkage factor is down to about 0.2%;Epoxy main chains after solidification is ehter bond, phenyl ring, three-dimensional crosslinking structure, therefore has excellence
Resistance to acids and bases.
Therefore, epoxy resin is widely used in the every field of national economy: either high-technology field is still
Field of general technology, either all can see its trace in defence and military or civilian industry, or even daily life.
At present, epoxy-resin systems there is also some problems, as thermostability is relatively low, far away not as good as heteroaromatic Type of Collective object
System's (such as polyimides, polybenzimidazoles, polybenzoxazole, polyphenylene quinoline, polybenzothiozole etc.).
Polyimides is developed in the sixties, and the most frequently used one is by pyromellitic acid anhydride and aromatic diamine system
?.Containing multiple aromatic heterocycle construction unit in polyimide molecule, therefore polyimide resin is to have extremely superior heat resistance
One family macromolecule material of property.Conventional polyimide structures, its heat decomposition temperature, generally individually more than 500 DEG C, also has simultaneously
There is obdurability.Therefore, being also frequently utilized for thermosetting resin, heat-resisting toughness reinforcing such as epoxy resin, bimaleimide resin etc. changes
Property agent.
Chinese invention patent CN103146330A discloses double [4-(2,4-diamino phenoxy) phenyl] six of a kind of 2,2-
Fluoro-propane type high temperature resistant epoxy adhesive and preparation method thereof, component A and B component by mass ratio is 1:1-2 form, wherein, A
Component is the copolymer reacted with epoxy resin by double [4-(2,4-diamino phenoxy) phenyl] HFC-236fa of 2,2-;B
Component be by double [4-(2,4-diamino phenoxy) phenyl] HFC-236fa of 2,2-with aromatic dicarboxylic anhydride in highly polar non-matter
The solid content reacted in sub-organic solvent and toluene is the homogeneous phase transparent solution of 15%-30%.Preparation method includes: room temperature
Under, A, B component 1:1-2 in mass ratio is uniformly mixed.
It is resistance to that Chinese invention patent CN103131369A discloses double (2,4-diamino phenoxy) the diphenyl sulphone (DPS) type of a kind of 4,4'-
High-temp epoxy adhesive and preparation method thereof, component A and B component by mass ratio is 1:1-2 form, and wherein component A is by 4,
The copolymer that 4 '-bis-(2,4-diamino phenoxy) diphenyl sulphone (DPS)s react with epoxy resin;B component is by 4,4 '-bis-(2,4-
Diamino phenoxy) diphenyl sulphone (DPS) and consolidating that aromatic dicarboxylic anhydride reacts in highly polar aprotic organic solvent and toluene
Content is the homogeneous phase transparent solution of 15%-30%.Preparation method includes: under room temperature, is stirred by A, B component 1:1-2 in mass ratio
Mix homogeneously.
Chinese invention patent CN103146331A discloses double (2,4-diamino phenoxy) the resistance to height of biphenyl type of a kind of 4,4'-
Temperature epoxy adhesive and preparation method thereof, component A and B component by mass ratio is 1:1-2 form, wherein component A be by 4,4 '-
The copolymer that double (2,4-diamino phenoxy) biphenyl reacts with epoxy resin;B component is by 4,4 '-bis-(2,4-diaminos
Phenoxyl) solid content that reacts in highly polar aprotic organic solvent and toluene with aromatic dicarboxylic anhydride of biphenyl is
The homogeneous phase transparent solution of 15%-30%.Preparation method includes: under room temperature, by A, B component 1:1-2 in mass ratio stirring mixing all
Even.
Yan Rui, Yu Xinhai et al. [preparation of novel epoxy adhesive and performance study, insulant, 2012,45 (2):
12-14,18] disclose a kind of neo-epoxy resin adhesive and preparation method thereof, and its performance has been carried out systematic research.
Yu Xinhai et al. [preparation of organosilicon epoxy system binding agent and performance study, insulant, 2012,45 (2):
1-3,11] disclose the adhesive composition of a kind of organic siliconresin modified epoxy, and its performance is studied, simultaneously
Obtain the binding agent that combination property is superior.
Yu Xinhai et al. has applied for Chinese invention patent CN102220102A, discloses a kind of high-temperature-resistant adhesive and system thereof
Preparation Method.
Chinese invention patent CN102260480A discloses a kind of high-temperature-resistant modified epoxy resin adhesive and preparation side thereof
Method.
Chinese invention patent CN102181251A discloses the epoxyn that a kind of unsaturated polyimides is modified
And preparation method thereof.
Chinese invention patent CN102031082A discloses a kind of benzimidazole diamine curing type epoxy adhesive and system thereof
Preparation Method.
Chinese invention patent CN101649174A discloses a kind of high temperature resistant one-component solvent-free epoxy adhesive and system thereof
Preparation Method.
Chinese invention patent CN101544879A discloses the preparation method of a kind of high strength solventless epoxy adhesive.
Wu Min et al. [development of novel high-strength one-component epoxy resin adhesive, bonding, 2009,30 (9): 54-57]
Disclose a kind of epoxy binder in monocomponent in, excellent combination property, particularly there is the highest tensile shear strength.
Chen Hongjiang et al. [the cure kinetics research of neo-epoxy resin adhesive system, bonding, 2009,30 (8): 43-
45] disclose a kind of epoxyn system, and its cure kinetics is studied.
Xu Meifang et al. [the cure kinetics research of polyimide-epoxy resin adhesive, chemistry and bonding, 2011,33
(2): 17-20] disclose a kind of polyimide-epoxy resin adhesive, and it has been carried out cure kinetics research.
Chinese invention patent CN101148656A, discloses the preparation method of a kind of heat-resistant solvent-free epoxy adhesive, its
It is characterized mainly in that: TGDDM epoxy resin, toughener, hydrogenated bisphenol A, firming agent, accelerator mix homogeneously, has prepared resistance to height
Temperature non-solvent epoxy adhesive.But its resistance to elevated temperatures still has bigger limitation, fail to meet under many hot environments
Actual application.
Chinese invention patent CN101397486A, discloses the preparation side of a kind of bi-component solvent-free epoxy resin adhesive
Method, is primarily characterized in that: it includes component A and B component, and wherein component A contains novolac epoxy resin, alicyclic type epoxy resin
And nbr carboxyl terminal;B component is double (2,4-diamino phenoxy) the benzene aromatic polyvalent amine hardener of 1,3-.Alicyclic ring type ring
The addition of epoxy resins and nbr carboxyl terminal is respectively the 20-35% and 12% (mass percent) of novolac epoxy resin.
The 15-20% that addition is novolac epoxy resin of double (2,4-diamino phenoxy) the benzene aromatic polyvalent amine hardener of 1,3-
(mass percent), gained adhesive system good manufacturability.But its heat resistance is the most preferable.
Chinese invention patent CN1927908A, discloses the preparation method of a kind of phenolic hydroxyl group containing polyimide powder, due to
The existence of phenolic hydroxyl group, its polyimide powder can form covalent bond with epoxy reaction, such that it is able to it is sub-to improve thermoplasticity polyamides
The compatibility of polyimide resin and epoxy resin, and epoxy-resin systems can be made further to reach good toughening effect.
Yu Xinhai et al. [development [J] of high-temperature resistant single-component epoxy adhesive. bonding, 2008,29 (12): 16-19] public
Open the preparation method of a kind of high-temperature resistant single-component epoxy adhesive, be primarily characterized in that: with maleic anhydride (MA) for end-blocking
Agent, with 2, double (3-amino-4-hydroxylphenyl) HFC-236fa (BAHPFP) of 2-, 2, double [4-(4-amino-benzene oxygen) phenyl] third of 2-
Double [4-(3,4-di carboxyl phenyloxy) phenyl] propane dianhydride (BPADA) of alkane (BAPOPP), 2,2-is that main material synthesis obtains
Phenolic hydroxy group polyetherimide resin (HPEI);It it is resistant, toughened dose with the synthesized HPEI obtained, with N, N, N', N'-tetra-
Glycidyl-4,4'-MDA (TGDDM), hydrogenated bisphenol A epoxy resin (HBPAE), latent curing agent
Deng, preparation has obtained the high-temperature resistant single-component epoxy adhesive of excellent combination property.
Summary of the invention
The technical problem to be solved is to provide a kind of BDAPP type siliceous epoxy acid imide matrix resin and system thereof
Preparation Method, preparation technology of the present invention is simple, environmental friendliness, excellent combination property, can be widely applied to the metals such as steel, copper, aluminum with
And the bonding between the base material such as pottery, glass, polymer matrix composites, and glass fibre, aramid fiber, fibre reinforced are multiple
The preparation of condensation material, has good industrialization prospect.
A kind of BDAPP type siliceous epoxy acid imide matrix resin of the present invention, is 1-5:100:2-8:1-5 by mass ratio:
The 2,2-of 30-50 double [4-(2,4-diamino phenoxy) phenyl] propane BDAPP, epoxy resin, 3-aminopropyl tri-alkoxy silicon
Alkane, imide oligomer thing and firming agent composition;Wherein, imide oligomer thing is to be the 2 of 2:1:2 by mol ratio, double (the 3-ammonia of 2-
Base-4-hydroxy phenyl) HFC-236fa, double [4-(3,4-di carboxyl phenyloxy) phenyl] propane dianhydride of 2,2-and maleic anhydride reaction
And obtain.
Described 3-aminopropyltrialkoxysilane is selected from 3-aminopropyl trimethoxysilane, 3-aminopropyl triethoxysilane
In one or both mixture.
Described epoxy resin is selected from E-51 epoxy resin, E-44 epoxy resin, ES216 epoxy resin, ECC202 asphalt mixtures modified by epoxy resin
Fat, CE793 epoxy resin, glycidyl amine type epoxy resin, diglycidyl ether type epoxy resin, alicyclic type epoxy resin, phenol
One or more in aldehyde type epoxy resin, glycidyl ester type epoxy resin.
Described glycidyl amine type epoxy resin is selected from N, N, N ', N '-four glycidyl group-4,4 '-diaminourea hexichol first
Alkane epoxy resin, N, N, N ', N '-four glycidyl group-3,3 '-dimethyl-4,4 '-MDA epoxy resin, N,
N, N ', N '-four glycidyl group-3,3 '-diethyl-4,4 '-MDA epoxy resin, N, N, N ', N '-four shrinks
Glyceryl-3,3 '-two chloro-4,4 '-MDA epoxy resin, N, N, N ', N '-four glycidyl group-4,4 ' and-diamino
Yl diphenyl ether epoxy resin, N, N, N ', N '-four glycidyl group-4,4 '-DADPS epoxy resin, N, N, N ', N '-
Four glycidyl group-3,4 '-diaminodiphenyl ether epoxy resin, N, N, N ', N '-four glycidyl group-3,3 '-diaminourea hexichol
Sulfone epoxy resin, N, N, N ', N '-four glycidyl group-4,4 '-benzidine epoxy resin, N, N, N ', N '-four shrinks sweet
Oil base p-phenylenediamine epoxy resin, N, N, N ', N '-four glycidyl group m-diaminobenzene. epoxy resin, N, N, N ', N '-four shrinks
Glyceryl-1,4-double (4-amino-benzene oxygen) phenyl ring epoxy resins, N, N, N ', double (the 3-aminobenzene of N '-four glycidyl group-1,4-
Epoxide) phenyl ring epoxy resins, N, N, N ', N '-four glycidyl group-1,3-double (4-amino-benzene oxygen) phenyl ring epoxy resins, N, N, N ',
N '-four glycidyl group-1,3-double (3-amino-benzene oxygen) phenyl ring epoxy resins, N, N, N ', N '-four glycidyl group-1,4-is double
(2-trifluoromethyl-4-aminophenoxyl) phenyl ring epoxy resins, N, N, N ', N '-four glycidyl group-1,3-pair (2-trifluoromethyl-
4-amino-benzene oxygen) phenyl ring epoxy resins, N, N, N ', N ', O-five glycidyl-4,4 '-diaminourea-4 "-hydroxyl tritan.
Epoxy resin, N, N, N ', N '-four glycidyl group-2,2-double [4-(4-amino-benzene oxygen) phenyl] propane epoxy resin, N, N,
N ', N '-four glycidyl group-2,2-double [4-(4-amino-benzene oxygen) phenyl] HFC-236fa epoxy resin, N, N, N ', N '-four
Glycidyl-2,2-double [4-(3-amino-benzene oxygen) phenyl] propane epoxy resin, N, N, N ', N '-four glycidyl group-2,
2-double [4-(2-trifluoromethyl-4-aminophenoxyl) phenyl] propane epoxy resin, N, N, N ', N '-four glycidyl group-2,2-
Double [4-(3-amino-benzene oxygen) phenyl] HFC-236fa epoxy resin, N, N, N ', the double [4-(2-of N '-four glycidyl group-2,2-
Trifluoromethyl-4-aminophenoxyl) phenyl] HFC-236fa epoxy resin, N, N, N ', N '-four glycidyl group-4,4 '-bis-(4-
Amino-benzene oxygen) diphenyl ether epoxy resin, N, N, N ', N '-four glycidyl group-4,4 '-bis-(2-trifluoromethyl-4-aminobenzenes
Epoxide) diphenyl ether epoxy resin, N, N, N ', N '-four glycidyl group-4,4 '-bis-(4-amino-benzene oxygen) diphenyl sulphone (DPS) asphalt mixtures modified by epoxy resin
Fat, N, N, N ', N '-four glycidyl group-4,4 '-bis-(2-trifluoromethyl-4-aminophenoxyl) diphenyl sulphone (DPS) epoxy resin, N, N,
N ', N '-four glycidyl group-4,4 '-bis-(4-amino-benzene oxygen) diphenyl sulfide epoxy resin, N, N, N ', N '-four (+)-2,3-Epoxy-1-propanol
Base-4,4 '-bis-(2-trifluoromethyl-4-aminophenoxyl) diphenyl sulfide epoxy resin, N, N, N ', N '-four glycidyl group-4,
4 '-bis-(4-amino-benzene oxygen) diphenyl-methane epoxy resin, N, N, N ', N '-four glycidyl group-4,4 ' and-bis-(2-fluoroforms
Base-4-amino-benzene oxygen) diphenyl-methane epoxy resin, N, N, N ', N '-four glycidyl group-4,4 '-bis-(4-amino-benzene oxygens)
Benzophenone epoxy resin, N, N, N ', N '-four glycidyl group-4,4 ' and-bis-(2-trifluoromethyl-4-aminophenoxyl) hexichol
Ketone epoxy resin, N, N, N ', N '-four glycidyl group-4,4 '-bis-(4-amino-benzene oxygen) biphenyl epoxy resin, N, N, N ',
N '-four glycidyl group-4,4 '-bis-(2-trifluoromethyl-4-aminophenoxyl) biphenyl epoxy resin, N, N, N ', N ', O, O '-
Six glycidyl-2,2-double (3-amino-4-hydroxylphenyl) HFC-236fa epoxy resin, N, N, O triglycidyl group is to ammonia
Base phenol epoxy resin, N, one or more in N, O triglycidyl meta-aminophenol epoxy resin.
Described diglycidyl ether type epoxy resin is selected from 1,3-diglycidyl resorcinol, 1,4-diglycidyl
Double (4-glycidyl phenyl) HFC-236fa of hydroquinone, 4,4 '-diglycidyl bisphenol S, 2,2-, 2,2-are double, and (4-contracts
Water glyceryl cyclohexyl) propane, Bisphenol F diglycidyl ether, hydrogenated bisphenol A diglycidyl ether, bisphenol-A 2-glycidyl
One or more in ether, fatty alcohol polyglycidyl ether.
Described alicyclic type epoxy resin is selected from 3,4-epoxycyclohexyethylSiOi acid-3 ', 4 '-epoxycyclohexyethylSiOi methyl ester, 3,4-epoxy
One or more in base-6-methyl cyclohexane acid-3 ', 4 '-epoxy radicals-6 '-methyl cyclohexane methyl ester, Dipentenedioxide.
Described phenol aldehyde type epoxy resin is selected from P-F phenolic resin type epoxy resin, o-cresol-formaldehyde novolac tree
Epoxy-type epoxy resin, resorcinol-formaldehyde phenolic resin type epoxy resin, m-cresol-formaldehyde phenolic resin type epoxy resin,
Catechol-formaldehyde phenolic resin type epoxy resin, bisphenol A-formaldehyde phenolic resin type epoxy resin, bisphenol S-formaldehyde novolac tree
Epoxy-type epoxy resin, bisphenol AF-formaldehyde phenolic resin type epoxy resin, '-biphenyl diphenol-formaldehyde phenolic resin type epoxy resin, neighbour
One or more in phenylphenol-formaldehyde phenolic resin type epoxy resin, naphthols-formaldehyde phenolic resin type epoxy resin.
Described glycidyl ester type epoxy resin is selected from terephthalic acid diglycidyl ester epoxy resin, M-phthalic acid
2-glycidyl ester epoxy resin, o-phthalic acid diglycidyl ester epoxy resin, interior methine tetrahydrophthalic acid two
Ethylene oxidic ester epoxy resin, 4,5-7-oxa-bicyclo[4.1.0-1,2-dioctyl phthalate 2-glycidyl ester epoxy resin, adjacent benzene two octanoic acid two
One or more in polyglycidyl epoxy resin.
Described firming agent is selected from HHPA, K-12 firming agent, THPA, methyl tetrahydro phthalic anhydride, dodecenyl succinate
Anhydride, methyl hexahydrophthalic anhydride, tung oil acid anhydride, with dicyclopentadiene and 80 anhydride of maleic acid anhydride reactant, with terpene two
The anhydride of alkene and maleic acid anhydride reactant, the liquid anhydride with Oleum Terebinthinae and maleic acid anhydride reactant, N, N-
Dimethylaniline, N, N-dimethyl open-chain crown ether, N, N-dimethyl benzylamine, 2-ethyl-4-methylimidazole, imidazoles, 2,4,6-
One or more in three (dimethylamino methyl) phenol, 1,8-diaza-dicyclo [5.4.0] hendecene-7.
The preparation method of a kind of BDAPP type siliceous epoxy acid imide matrix resin of the present invention, comprises the steps:
(1) by double for 2,2-(3-amino-4-hydroxylphenyl) HFC-236fa, orthoresol, double [4-(the 3,4-dicarboxyl benzene of 2,2-
Epoxide) phenyl] propane dianhydride and maleic anhydride put in reactor, is passed through nitrogen, stirring, and it is heated to 80 DEG C, drips different
Quinoline, is heated to 100 DEG C-110 DEG C, after stirring is reacted 5-12 hour, is cooled to 60 DEG C, is poured into by reactant and fill precipitating agent
In precipitating still, high-speed stirred, separate out solids, filter, 80 DEG C are vacuum dried 10 hours, obtain imide oligomer thing;
(2) double for 2,2-[4-(2,4-diamino phenoxy) phenyl] propane (BDAPP), epoxy resin are put into reactor
In, after 80 DEG C-100 DEG C stirring hybrid reactions 0.5-1 hour, add imide oligomer thing and continue stirring reaction 1-2 hour, with
Rear addition 3-aminopropyltrialkoxysilane stirring reaction 5-15 minute, is cooled to room temperature, adds firming agent, and stirring mixing is all
Even.
The mass ratio of (3-amino-4-hydroxylphenyl) HFC-236fa double with 2,2-of the isoquinolin described in step (1) is 1-
4:20。
Precipitating agent described in step (1) is selected from methanol, ethanol, propanol, isopropanol, ethylene glycol, glycol monoethyl ether, second
One or more in glycol dimethyl ether, ethylene glycol monoethyl ether, ethylene glycol diethyl ether, acetone, butanone;Wherein, precipitating agent and 2,
The mass ratio of double (3-amino-4-hydroxylphenyl) HFC-236fa of 2-is 20-40:1.
The mass ratio of (3-amino-4-hydroxylphenyl) HFC-236fa double with 2,2-of the orthoresol described in step (1) is 10-
20:1。
Beneficial effect
(1) viscosity controllability of the present invention is good, can regulate in broader scope, and preparation technology is simple, environmental friendliness, combines
Close excellent performance, can be widely applied between the base material such as the metals such as steel, copper, aluminum and pottery, glass, polymer matrix composites
Bonding, and the preparation of glass fibre, aramid fiber, carbon fibre reinforced composite, have good industrialization prospect;
(2) present invention can complete preparation process in common apparatus, is advantageously implemented industrialized production.
Detailed description of the invention
Below in conjunction with specific embodiment, the present invention is expanded on further.Should be understood that these embodiments are merely to illustrate the present invention
Rather than restriction the scope of the present invention.In addition, it is to be understood that after having read the content that the present invention lectures, people in the art
The present invention can be made various changes or modifications by member, and these equivalent form of values fall within the application appended claims equally and limited
Scope.
Embodiment 1
By 73.2 grams of (0.2 moles) 2, double (3-amino-4-hydroxylphenyl) HFC-236fa (BAHPFP, 366g/mol) of 2-,
735.0 grams of orthoresols, 52.0 grams of (0.1 moles) 2, double [4-(3, the 4-di carboxyl phenyloxy) phenyl] propane dianhydride of 2-(BPADA,
520g/mol) He 19.6 grams (0.2 mole) maleic anhydride (MA, 98g/mol) put in reactor, are passed through nitrogen, stirring, heating
It is warming up to 80 DEG C, drips 3.8 grams of isoquinolin, be heated to 100 DEG C, after stirring is reacted 5 hours, be cooled to 60 DEG C, reactant is fallen
Enter in the precipitating still filling 1500 grams of methanol, high-speed stirred, separate out solids, filter, 80 DEG C are vacuum dried 10 hours, obtain
308.3 grams of imide oligomer things (theoretical yield: 314.0 grams), yield 98.2%, it is denoted as BBMO-1.
Embodiment 2
By 73.2 grams of (0.2 moles) 2, double (3-amino-4-hydroxylphenyl) HFC-236fa (BAHPFP, 366g/mol) of 2-,
1460 grams of orthoresols, 52.0 grams of (0.1 moles) 2, double [4-(3, the 4-di carboxyl phenyloxy) phenyl] propane dianhydride of 2-(BPADA,
520g/mol) He 19.6 grams (0.2 mole) maleic anhydride (MA, 98g/mol) put in reactor, are passed through nitrogen, stirring, heating
It is warming up to 80 DEG C, drips 14.0 grams of isoquinolin, be heated to 110 DEG C, after stirring is reacted 12 hours, be cooled to 60 DEG C, by reactant
Pour in the precipitating still filling 2000 grams of ethanol and 920 grams of glycol monoethyl ethers, high-speed stirred, separate out solids, filter, 80 DEG C
It is vacuum dried 10 hours, obtains 313.4 grams of imide oligomer things (theoretical yield: 314.0 grams), yield 99.8%, be denoted as BBMO-
2。
Embodiment 3
Double for 1.0 grams of 2,2-[4-(2,4-diamino phenoxy) phenyl] propane (BDAPP), 40.0 grams of 1,3-bis-are shunk sweet
Oil base resorcinol, 20.0 grams of CE793 epoxy resin, 10.0 grams of 3,4-epoxycyclohexyethylSiOi acid-3 ', 4 '-epoxycyclohexyethylSiOi methyl ester
With 30.0 grams of N, N, N ', double [4-(4-amino-benzene oxygen) phenyl] the HFC-236fa epoxy resin of N '-four glycidyl group-2,2-is put
Enter in reactor, after 100 DEG C of stirring hybrid reactions 0.5 hour, add 2.0 grams of BBMO-1 imide oligomer things and continue stirring instead
Answer 1 hour, be subsequently added 3.0 grams of 3-aminopropyl trimethoxysilane stirring reactions 5 minutes, be cooled to room temperature, add 8.0 grams
1,8-diaza-dicyclo [5.4.0] hendecene-7,12.0 grams of methyl tetrahydro phthalic anhydrides and 30.0 grams of tung oil acid anhydrides, stirring mixing is all
Even, obtain 156.0 grams of BDAPP type siliceous epoxy acid imide matrix resins, be denoted as M-1.
Embodiment 4
By double for 3.0 grams of 2,2-[4-(2,4-diamino phenoxy) phenyl] propane (BDAPP), 10.0 grams of 3,4-epoxy basic rings
Caproic acid-3 ', 4 '-epoxycyclohexyethylSiOi methyl ester, 10.0 grams of Diglycidyl M-phthalate epoxy resin, 20.0 grams of ES216 rings
Epoxy resins, 50.0 grams of N, N, N ', double [4-(4-amino-benzene oxygen) phenyl] the propane epoxy resin of N '-four glycidyl group-2,2-
With 10.0 grams of N, N, N ', N '-four glycidyl group-4,4 '-diaminodiphenyl ether epoxy resin is put in reactor, stirs in 80 DEG C
After mixing hybrid reaction 1 hour, the imide oligomer thing continuation stirring reaction 2 adding 3.0 grams of BBMO-1 and 2.0 grams of BBMO-2 is little
Time, it is subsequently added 4.0 grams of 3-aminopropyl trimethoxysilane and 4.0 grams of 3-aminopropyl triethoxysilane stirrings is reacted 5 minutes,
It is cooled to room temperature, adds 10.0 grams of 2-ethyl-4-methylimidazoles, 10.0 grams of dodecenylsuccinic anhydrides and 10.0 gram 2,4,6-
Three (dimethylamino methyl) phenol, is uniformly mixed, and obtains 146.0 grams of BDAPP type siliceous epoxy acid imide matrix resins, note
Make M-2.
Embodiment 5
By double for 5.0 grams of 2,2-[4-(2,4-diamino phenoxy) phenyl] propane (BDAPP), 10.0 grams of N, N, O tri-shrinks
Glyceryl para-aminophenol epoxy resin, 10.0 grams of o-cresol-formaldehyde phenolic resin type epoxy resin, 10.0 grams of A Hydrogenated Bisphenol As
A diglycidyl ether, 30.0 grams of 4,5-7-oxa-bicyclo[4.1.0-1,2-dioctyl phthalate 2-glycidyl ester epoxy resins and 40.0 grams of N, N,
N ', N '-four glycidyl group-4,4 '-MDA epoxy resin is put in reactor, stirs hybrid reaction in 80 DEG C
After 1 hour, the imide oligomer thing adding 3.0 grams of BBMO-2 continues stirring reaction 2 hours, is subsequently added 2.0 grams of 3-aminopropyls
Trimethoxy silane stirring reaction 15 minutes, is cooled to room temperature, adds 25.0 grams of 2-ethyl-4-methylimidazoles and 20.0 gram six
Hydrogen phthalic anhydride, is uniformly mixed, and obtains 155.0 grams of BDAPP type siliceous epoxy acid imide matrix resins, is denoted as M-3.
Embodiment 6
Take the BDAPP type siliceous epoxy acid imide matrix resin of appropriate embodiment 3~embodiment 5, i.e. M-1~M-respectively
3, and be uniformly applied to respectively in standard rustless steel test piece, overlapping, clamping, put in convection oven and solidify: from room temperature
Start to warm up to 80 DEG C, after keeping 2 hours, be continuously heating to 120 DEG C, after keeping 1 hour, be continuously heating to 150 DEG C, keep
After 0.5 hour, naturally cool to room temperature.Utilize electronic tensile machine, respectively it is carried out room temperature (25 DEG C) and high temperature (180 DEG C) bar
Tensile shear strength test under part, result is as shown in table 1.
Take the BDAPP type siliceous epoxy acid imide matrix resin of appropriate embodiment 3~embodiment 5, i.e. M-1~M-respectively
3, and be uniformly applied to respectively in plate glass test piece, overlapping, clamping, put in convection oven and solidify: open from room temperature
Begin to be warming up to 80 DEG C, after keeping 2 hours, be continuously heating to 120 DEG C, after keeping 1 hour, be continuously heating to 150 DEG C, keep 0.5
After hour, naturally cool to room temperature.Utilize electronic tensile machine, respectively it is carried out room temperature (25 DEG C) and high temperature (180 DEG C) condition
Under tensile shear strength test, result is as shown in table 1.
Take the BDAPP type siliceous epoxy acid imide matrix resin of appropriate embodiment 3~embodiment 5, i.e. M-1~M-respectively
3, and be impregnated with the most equably on glass cloth, with standard rustless steel test piece overlapping clamping, put in convection oven and solidify:
Start to warm up to 80 DEG C from room temperature, after keeping 2 hours, be continuously heating to 120 DEG C, after keeping 1 hour, be continuously heating to 150 DEG C,
After keeping 0.5 hour, naturally cool to room temperature.Utilize electronic tensile machine, respectively it is carried out room temperature (25 DEG C) and high temperature (180
DEG C) under the conditions of tensile shear strength test, result is as shown in table 1.
Table 1 tensile shear strength, unit: MPa
Claims (10)
1. a BDAPP type siliceous epoxy acid imide matrix resin, it is characterised in that: be 1-5:100:2-8:1-5 by mass ratio:
The 2,2-of 30-50 double [4-(2,4-diamino phenoxy) phenyl] propane BDAPP, epoxy resin, 3-aminopropyl tri-alkoxy silicon
Alkane, imide oligomer thing and firming agent composition;Wherein, imide oligomer thing is to be the 2 of 2:1:2 by mol ratio, double (the 3-ammonia of 2-
Base-4-hydroxy phenyl) HFC-236fa, double [4-(3,4-di carboxyl phenyloxy) phenyl] propane dianhydride of 2,2-and maleic anhydride reaction
And obtain.
A kind of BDAPP type siliceous epoxy acid imide matrix resin the most according to claim 1, it is characterised in that: described 3-
Aminopropyltrialkoxysilane is selected from one or both in 3-aminopropyl trimethoxysilane, 3-aminopropyl triethoxysilane
Mixture.
A kind of BDAPP type siliceous epoxy acid imide matrix resin the most according to claim 1, it is characterised in that: described ring
Epoxy resins is selected from E-51 epoxy resin, E-44 epoxy resin, ES216 epoxy resin, ECC202 epoxy resin, CE793 asphalt mixtures modified by epoxy resin
Fat, glycidyl amine type epoxy resin, diglycidyl ether type epoxy resin, alicyclic type epoxy resin, phenol aldehyde type epoxy resin, contracting
One or more in water glycerol ester type epoxy resin.
A kind of BDAPP type siliceous epoxy acid imide matrix resin the most according to claim 3, it is characterised in that: described contracting
Water glycerol amine type epoxy resin is selected from N, N, N ', N '-four glycidyl group-4,4 '-MDA epoxy resin, N, N,
N ', N '-four glycidyl group-3,3 '-dimethyl-4,4 '-MDA epoxy resin, N, N, N ', N '-four shrinks sweet
Oil base-3,3 '-diethyl-4,4 '-MDA epoxy resin, N, N, N ', N '-four glycidyl group-3,3 '-two
Chloro-4,4 '-MDA epoxy resin, N, N, N ', N '-four glycidyl group-4,4 ' and-diaminodiphenyl ether asphalt mixtures modified by epoxy resin
Fat, N, N, N ', N '-four glycidyl group-4,4 '-DADPS epoxy resin, N, N, N ', N '-four glycidyl group-3,
4 '-diaminodiphenyl ether epoxy resin, N, N, N ', N '-four glycidyl group-3,3 '-DADPS epoxy resin, N, N,
N ', N '-four glycidyl group-4,4 '-benzidine epoxy resin, N, N, N ', N '-four glycidyl group p-phenylenediamine epoxy
Resin, N, N, N ', N '-four glycidyl group m-diaminobenzene. epoxy resin, N, N, N ', the double (4-of N '-four glycidyl group-1,4-
Amino-benzene oxygen) phenyl ring epoxy resins, N, N, N ', double (3-amino-benzene oxygen) the phenyl ring epoxy resins of N '-four glycidyl group-1,4-,
N, N, N ', N '-four glycidyl group-1,3-double (4-amino-benzene oxygen) phenyl ring epoxy resins, N, N, N ', N '-four glycidyl group-
1,3-double (3-amino-benzene oxygen) phenyl ring epoxy resins, N, N, N ', the double (2-trifluoromethyl-4-ammonia of N '-four glycidyl group-1,4-
Phenoxyl) phenyl ring epoxy resins, N, N, N ', double (2-trifluoromethyl-4-aminophenoxyl) benzene of N '-four glycidyl group-1,3-
Epoxy resin, N, N, N ', N ', O-five glycidyl-4,4 '-diaminourea-4 "-hydroxyl tritan. epoxy resin, N, N, N ',
N '-four glycidyl group-2,2-double [4-(4-amino-benzene oxygen) phenyl] propane epoxy resin, N, N, N ', N '-four (+)-2,3-Epoxy-1-propanol
Base-2,2-double [4-(4-amino-benzene oxygen) phenyl] HFC-236fa epoxy resin, N, N, N ', N '-four glycidyl group-2,2-is double
[4-(3-amino-benzene oxygen) phenyl] propane epoxy resin, N, N, N ', double [4-(the 2-fluoroform of N '-four glycidyl group-2,2-
Base-4-amino-benzene oxygen) phenyl] propane epoxy resin, N, N, N ', double [4-(the 3-aminobenzene oxygen of N '-four glycidyl group-2,2-
Base) phenyl] HFC-236fa epoxy resin, N, N, N ', the double [4-(2-trifluoromethyl-4-aminobenzene of N '-four glycidyl group-2,2-
Epoxide) phenyl] HFC-236fa epoxy resin, N, N, N ', N '-four glycidyl group-4,4 '-bis-(4-amino-benzene oxygen) diphenyl ether
Epoxy resin, N, N, N ', N '-four glycidyl group-4,4 ' and-bis-(2-trifluoromethyl-4-aminophenoxyl) diphenyl ether asphalt mixtures modified by epoxy resin
Fat, N, N, N ', N '-four glycidyl group-4,4 '-bis-(4-amino-benzene oxygen) diphenyl sulphone (DPS) epoxy resin, N, N, N ', N '-four contracts
Water glyceryl-4,4 '-bis-(2-trifluoromethyl-4-aminophenoxyl) diphenyl sulphone (DPS) epoxy resin, N, N, N ', N '-four (+)-2,3-Epoxy-1-propanol
Base-4,4 '-bis-(4-amino-benzene oxygen) diphenyl sulfide epoxy resin, N, N, N ', N '-four glycidyl group-4,4 '-bis-(2-tri-
Methyl fluoride-4-amino-benzene oxygen) diphenyl sulfide epoxy resin, N, N, N ', N '-four glycidyl group-4,4 '-bis-(4-aminobenzenes
Epoxide) diphenyl-methane epoxy resin, N, N, N ', N '-four glycidyl group-4,4 '-bis-(2-trifluoromethyl-4-aminophenoxyls)
Diphenyl-methane epoxy resin, N, N, N ', N '-four glycidyl group-4,4 ' and-bis-(4-amino-benzene oxygen) benzophenone asphalt mixtures modified by epoxy resin
Fat, N, N, N ', N '-four glycidyl group-4,4 '-bis-(2-trifluoromethyl-4-aminophenoxyl) benzophenone epoxy resin, N,
N, N ', N '-four glycidyl group-4,4 '-bis-(4-amino-benzene oxygen) biphenyl epoxy resin, N, N, N ', N '-four (+)-2,3-Epoxy-1-propanol
Base-4,4 '-bis-(2-trifluoromethyl-4-aminophenoxyl) biphenyl epoxy resin, N, N, N ', N ', O, O '-six glycidyl-
2,2-double (3-amino-4-hydroxylphenyl) HFC-236fa epoxy resin, N, N, O triglycidyl group para-aminophenol asphalt mixtures modified by epoxy resin
Fat, N, one or more in N, O triglycidyl meta-aminophenol epoxy resin.
A kind of BDAPP type siliceous epoxy acid imide matrix resin the most according to claim 3, it is characterised in that: described contracting
Water ethoxylated glycerol type epoxy resin selected from 1,3-diglycidyl resorcinol, 1,4-diglycidyl hydroquinone, 4,4 '-
Double (4-glycidyl phenyl) HFC-236fa of diglycidyl bisphenol S, 2,2-, 2,2-are double (4-glycidyl cyclohexyl)
Propane, Bisphenol F diglycidyl ether, hydrogenated bisphenol A diglycidyl ether, bisphenol A diglycidyl ether, the many shrinks of fatty alcohol are sweet
One or more in oil ether.
A kind of BDAPP type siliceous epoxy acid imide matrix resin the most according to claim 3, it is characterised in that: described fat
Ring-like epoxy resin is selected from 3,4-epoxycyclohexyethylSiOi acid-3 ', 4 '-epoxycyclohexyethylSiOi methyl ester, 3,4-epoxy radicals-6-methyl cyclohexane
One or more in acid-3 ', 4 '-epoxy radicals-6 '-methyl cyclohexane methyl ester, Dipentenedioxide.
A kind of BDAPP type siliceous epoxy acid imide matrix resin the most according to claim 3, it is characterised in that: described phenol
Aldehyde type epoxy resin selected from P-F phenolic resin type epoxy resin, o-cresol-formaldehyde phenolic resin type epoxy resin,
Resorcinol-formaldehyde phenolic resin type epoxy resin, m-cresol-formaldehyde phenolic resin type epoxy resin, catechol-formaldehyde
Phenolic resin type epoxy resin, bisphenol A-formaldehyde phenolic resin type epoxy resin, bisphenol S-formaldehyde phenolic resin type epoxy resin,
Bisphenol AF-formaldehyde phenolic resin type epoxy resin, '-biphenyl diphenol-formaldehyde phenolic resin type epoxy resin, o-phenyl phenol-formaldehyde
One or more in phenolic resin type epoxy resin, naphthols-formaldehyde phenolic resin type epoxy resin.
A kind of BDAPP type siliceous epoxy acid imide matrix resin the most according to claim 3, it is characterised in that: described contracting
Water glycerol ester type epoxy resin is selected from terephthalic acid diglycidyl ester epoxy resin, Diglycidyl M-phthalate ring
Epoxy resins, o-phthalic acid diglycidyl ester epoxy resin, interior methine tetrahydrophthalic acid 2-glycidyl ester epoxy
Resin, 4,5-7-oxa-bicyclo[4.1.0-1,2-dioctyl phthalate 2-glycidyl ester epoxy resin, adjacent benzene two octanoic acid diglycidyl ether asphalt mixtures modified by epoxy resin
One or more in fat.
A kind of BDAPP type siliceous epoxy acid imide matrix resin the most according to claim 1, it is characterised in that: described solid
Agent is selected from HHPA, K-12 firming agent, THPA, methyl tetrahydro phthalic anhydride, dodecenylsuccinic anhydride, methyl hexahydrobenzene
Acid anhydride, tung oil acid anhydride, with dicyclopentadiene and 80 anhydride of maleic acid anhydride reactant, with limonene and maleic anhydride
The anhydride of reaction, the liquid anhydride with Oleum Terebinthinae and maleic acid anhydride reactant, N, accelerine, N, N-bis-
Methyl open-chain crown ether, N, N-dimethyl benzylamine, 2-ethyl-4-methylimidazole, imidazoles, 2,4,6-tri-(dimethylamino methyl) benzene
One or more in phenol, 1,8-diaza-dicyclo [5.4.0] hendecene-7.
10. a preparation method for BDAPP type as claimed in claim 1 siliceous epoxy acid imide matrix resin, including as follows
Step:
(1) by double for 2,2-(3-amino-4-hydroxylphenyl) HFC-236fa, orthoresol, the double [4-(3,4-di carboxyl phenyloxy) of 2,2-
Phenyl] propane dianhydride and maleic anhydride put in reactor, is passed through nitrogen, stirring, and it is heated to 80 DEG C, drips isoquinolin,
It is heated to 100 DEG C-110 DEG C, after stirring is reacted 5-12 hour, is cooled to 60 DEG C, reactant is poured into the precipitating filling precipitating agent
In still, stirring, separate out solids, filter, vacuum drying, obtain imide oligomer thing;
(2) by 2, double [4-(2,4-diamino phenoxy) phenyl] the propane BDAPP of 2-, epoxy resin are put in reactor, in 80
After DEG C of-100 DEG C stirring hybrid reactions 0.5-1 hour, add imide oligomer thing and continue stirring reaction 1-2 hour, be subsequently added
3-aminopropyltrialkoxysilane stirring reaction 5-15 minute, is cooled to room temperature, adds firming agent, be uniformly mixed i.e.
Can.
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CN109370161A (en) * | 2018-11-22 | 2019-02-22 | 安徽汇创新材料有限公司 | A kind of preparation method of the glass toughening manure pit of corrosion-resistant cracking resistance |
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