CN103012779B - Benzoxazine resin/ionic liquid composition - Google Patents

Benzoxazine resin/ionic liquid composition Download PDF

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CN103012779B
CN103012779B CN201110280986.9A CN201110280986A CN103012779B CN 103012779 B CN103012779 B CN 103012779B CN 201110280986 A CN201110280986 A CN 201110280986A CN 103012779 B CN103012779 B CN 103012779B
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ionic liquid
benzoxazine
resin
butyl
benzoxazine colophony
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CN103012779A (en
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徐日炜
王维霞
吴一弦
余鼎声
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Beijing University of Chemical Technology
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Beijing University of Chemical Technology
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Abstract

The present invention relates to a benzoxazine resin/ionic liquid composition and preparation thereof, and a thermosetting resin composition containing the benzoxazine resin/ionic liquid composition, wherein a mass ratio of the ionic liquid to the benzoxazine resin is 0.1-50:99.9-50, the benzoxazine resin is a compound having a molecular structure containing a benzoxazine group or a substituted benzoxazine unit, a polymer or a mixture of the compound and the polymer, and the ionic liquid is an ionic liquid having an organic cationic saturated alkyl side chain. According to the present invention, the ionic liquid is added to the composition, such that a curing temperature of the benzoxazine resin can be substantially reduced.

Description

Benzoxazine resin/ionic liquid compositions
Technical field
The present invention relates to resin combination, be specifically related to benzoxazine resin/ionic liquid compositions, it effectively can reduce the solidification value of resin.
Background technology
Benzoxazine is a kind of novel modification heterocyclic phenol, and it is the class novel hot setting resin grown up on the basis of traditional resol., under heating and/or catalytic condition, there is the crosslinking structure that ring-opening polymerization becomes a kind of similar resol in the class intermediate that it is is Material synthesis with phenolic compound, aldehydes and aminated compounds.Benzoxazine not only has the excellent properties of traditional resol but also it does not have small molecules to release in the curing process, goods zero shrink, and polymkeric substance has the special benefits of good thermotolerance, mechanical property, high thermal resistance, moisture resistance and has molecule designability flexibly.
You closes the background technology of benzoxazine and primary synthetic methods thereof can with reference in " containing the allylic benzoxazine intermediate of N-and composition and method of making the same " (Chinese Patent Application No. 03146797.0), " phenolphthalein type benzoxazine intermediate and composition and method of making the same " (Chinese Patent Application No. 200510087724.5), " silsesquioxane and its composition and preparation method containing benzoxazinyl group " (Chinese Patent Application No. 200610114117.8), " 2-oxazoline-Ben Bing Evil compounds and its composition and preparation method " (Chinese Patent Application No. 200610114118.2) and " benzoxazine colophony and composition and method of making the same based on renewable resources " content described in (Chinese Patent Application No. 200910143891.5).
Although benzoxazine has excellent performance, its solidification value is still higher, which has limited its application.For reducing the solidification value of benzoxazine, have already been proposed a variety of method.Such as, Y X Wang reported the ring-opening polymerization of catalysis benzoxazine (Y X Wang and H Ishida, Polymer, 1999 such as phosphorus pentachloride, phosphorus trichloride, dichloro oxygen phosphorus, titanium tetrachloride, aluminum chloride, p-methyl benzenesulfonic acid methyl esters in 1999,40,4563).Within 1999, J Dunkers then adopts the catalysis benzoxazine ring-opening polymerizations (J Dunkers and H Ishida, J.Polym.Sci.Part A.Polym.Chem., 1999,37,1913) such as acetic acid, hexanodioic acid, trifluoroacetic acid, p-cresol; Above-mentioned cation ring-opening polymerization catalyzer is used for benzoxazine ring-opening polymerization or curing reaction by calendar year 2001 Ishida in United States Patent (USP) 6225440.
The salt that normally relatively large by volume, the asymmetric organic cation of ionic liquid and the relatively little inorganic anion of volume are formed, they have the incomparable uniqueness of a lot of molecular solvent, wherein most study, what be most widely used is a class at room temperature or the ionic liquid to be in a liquid state under being bordering on room temperature (lower than 100 DEG C).Ionic liquid mainly comprise imidazoles, pyridines, season phosphonium salt class, quaternary ammonium salt, pyrrolidines, piperidines, all multiple types such as morpholine class ionic liquid, its purposes is very extensive, relates to the numerous areas such as chemistry, material, biology, the energy.
Bisphenol A-type benzoxazine colophony is cross-linked by Kawauchi in 2008 etc. in ionic liquid, obtains Polybenzoxazine/hybridization of ionic liquid material, which uses ionic liquid 1-butyl-3-methyl imidazolium trifluoromethyl sulfonic acid; But do not notice that benzoxazine/ionic liquid compositions can significantly reduce its solidification value.(T.Kawauchi，M.Ohara，S.Hirai，T.Takeichi.Chemistry Letters，2008，37(11)，1132-1133)
Not yet have so far and anyly significantly reduce benzoxazine solidification value about benzoxazine resin/ionic liquid compositions, and gained solidify material has the report of good over-all properties.
Summary of the invention
The present inventor, through studying discovery with keen determination, by being mixed with ionic liquid by benzoxazine colophony, significantly can reduce the solidification value of benzoxazine colophony resin, and the excellent performance of resulting composition solidification resulting product.
The object of the present invention is to provide benzoxazine resin/ionic liquid compositions, wherein the mass ratio of ionic liquid and benzoxazine colophony is 0.1 ~ 50: 99.9 ~ 50,
Described benzoxazine colophony refers to the compound of the benzoxazine unit containing benzoxazine unit shown in following formula or replacement in molecular structure, polymkeric substance or their mixture,
Wherein, R can be hydrogen, alkyl, aryl, unsaturated alkyl (as thiazolinyl), alicyclic radical or other organic groups (as alkyl silyl, itrile group, hydroxyl, carboxyl, haloalkyl, halogen atom, ether, thioether group, carbonyl, sulfuryl etc.).
The ionic liquid of described ionic liquid to be organic cation side chain be saturated alkyl.
Another object of the present invention is to provide the benzoxazine resin/ionic liquid compositions according to above-mentioned, wherein said ionic liquid be selected from following in one or more:
Wherein, R 1it is the alkyl containing 1 ~ 20 carbon atom;
R 2h, alkyl containing 1 ~ 20 carbon atom, R 3the alkyl etc. containing 1 ~ 20 carbon atom, and R 2and R 3can be identical, also can be different;
R 4h, alkyl containing 1 ~ 20 carbon atom, R 5the alkyl containing 1 ~ 20 carbon atom, and R 4and R 5can be identical, also can be different;
R 6h, alkyl containing 1 ~ 20 carbon atom, R 7~ R 9the alkyl containing 1 ~ 20 carbon atom independently of one another, and R 6, R 7, R 8, and R 9each other can be identical or different;
R 10h, alkyl containing 1 ~ 20 carbon atom, R 11~ R 13the alkyl containing 1 ~ 20 carbon atom independently of one another, and R 10, R 11, R 12, and R 13each other can be identical or different;
R 14h, alkyl containing 1 ~ 20 carbon atom, R 15the alkyl containing 1 ~ 20 carbon atom, and R 14and R 15can be identical, also can be different; With
X -for bromine, helium, iodine, fluoroboric acid root, nitrate radical, hexafluoro-phosphate radical, trifluoromethanesulfonic acid root, sulfate radical, thiocyanate ion, perchlorate, carboxylate radical are (as oxalate, C 1~ C 20carboxylate radical).
Another aspect of the invention provides the preparation method of benzoxazine resin/ionic liquid compositions, and the method is undertaken by being mixed with ionic liquid by benzoxazine colophony.
Another object of the present invention is to provide the compositions of thermosetting resin containing benzoxazine resin/ionic liquid compositions, and it comprises: benzoxazine resin/ionic liquid compositions, and other thermosetting resins and/or filler.
By benzoxazine resin/ionic liquid compositions provided by the invention, significantly can reduce the solidification value of benzoxazine colophony, be easier to solidification, and gained cured article has excellent performance.
Accompanying drawing explanation
Fig. 1 is the DSC curve of gained benzoxazine resin/ionic liquid compositions in embodiment 1.
Fig. 2 is the DSC curve of gained benzoxazine resin/ionic liquid compositions in embodiment 2.
Fig. 3 is the DSC curve of gained benzoxazine resin/ionic liquid compositions in embodiment 3.
Fig. 4 is the DSC curve of gained benzoxazine resin/ionic liquid compositions in embodiment 4.
Fig. 5 is the DSC curve of gained benzoxazine resin/ionic liquid compositions in embodiment 5.
Fig. 6 is the DSC curve of gained benzoxazine colophony in comparative example 1.
Fig. 7 is the DSC curve of gained benzoxazine colophony in comparative example 2.
Embodiment
Below by way of embodiment, the present invention is described in detail, and illustrated by these, the features and advantages of the invention will become clearly, clearly.
According to an aspect of the present invention, provide benzoxazine resin/ionic liquid compositions, wherein the mass ratio of ionic liquid and benzoxazine colophony is 0.1 ~ 50: 99.9 ~ 50,
Described benzoxazine colophony refers to the compound of the benzoxazine unit containing benzoxazinyl group shown in following formula or replacement in molecular structure, polymkeric substance or their mixture,
Wherein, R can be hydrogen, alkyl, aryl, unsaturated alkyl (as thiazolinyl), alicyclic radical or other organic groups (as alkyl silyl, itrile group, hydroxyl, carboxyl, haloalkyl, halogen atom, ether, thioether group, carbonyl, sulfuryl etc.)
The ionic liquid of described ionic liquid to be organic cation side chain be saturated alkyl.
In benzoxazine resin/ionic liquid compositions according to the present invention, the mass ratio of ionic liquid and benzoxazine colophony is 0.1 ~ 50: 99.9 ~ 50, be preferably 0.1 ~ 20: 99.9 ~ 80, be more preferably 0.1 ~ 10: 99.9 ~ 90, particularly 0.1 ~ 5: 99.9 ~ 95.If the mass ratio of ionic liquid and benzoxazine colophony is less than 0.1: 99.9, the solidification value of benzoxazine colophony is then caused to reduce degree because ionic liquid consumption is too low inadequate, otherwise, if the mass ratio of ionic liquid and benzoxazine colophony is higher than 50: 50, the solidification of benzoxazine colophony is then affected because ionic liquid consumption is too high, thus deteriorated product properties.When ionic liquid and benzoxazine colophony mass ratio within the scope of the present invention time, the solidification value of resin can not only be reduced, and the excellent performance of cured article.
ionic liquid
In this article, term used " saturation type ionic liquid " or " ionic liquid " are meant to interchangeable, refer to that wherein organic cations side chain is the ionic liquid of saturated alkyl.
In preferred embodiments, described saturation type ionic liquid be selected from following in one or more:
Wherein, R 1it is the alkyl containing 1 ~ 20 carbon atom;
R 2h, alkyl containing 1 ~ 20 carbon atom, R 3the alkyl etc. containing 1 ~ 20 carbon atom, and R 2and R 3can be identical, also can be different;
R 4h, alkyl containing 1 ~ 20 carbon atom, R 5the alkyl containing 1 ~ 20 carbon atom, and R 4and R 5can be identical, also can be different;
R 6h, alkyl containing 1 ~ 20 carbon atom, R 7~ R 9the alkyl containing 1 ~ 20 carbon atom independently of one another, and R 6, R 7, R 8and R 9between each other can be identical or different;
R 10h, alkyl containing 1 ~ 20 carbon atom, R 11~ R 13the alkyl containing 1 ~ 20 carbon atom independently of one another, and R 10, R 11, R 12and R 13each other can be identical or different;
R 14h, alkyl containing 1 ~ 20 carbon atom, R 15the alkyl containing 1 ~ 20 carbon atom, and R 14and R 15can be identical, also can be different; With
X -for bromine, chlorine, iodine, fluoroboric acid root, nitrate radical, hexafluoro-phosphate radical, trifluoromethanesulfonic acid root, sulfate radical, thiocyanate ion, perchlorate, carboxylate radical are as oxalate, C 1~ C 20carboxylate radical.
In a further preferred embodiment, described saturation type ionic liquid be selected from following in one or more:
Wherein, R 1containing the alkyl, particularly methyl of 1-6 carbon atom, ethyl, propyl group, butyl and hexyl;
R 2h, alkyl, particularly methyl containing 1 ~ 6 carbon atom, ethyl, propyl group, butyl and hexyl, R 3the alkyl containing 1 ~ 6 carbon atom, and R 2and R 3can be identical, also can be different;
R 4h, alkyl, particularly methyl containing 1 ~ 6 carbon atom, ethyl, propyl group, butyl and hexyl, R 5containing the alkyl, particularly methyl of 1 ~ 6 carbon atom, ethyl, propyl group, butyl and hexyl, and R 4and R 5can be identical, also can be different;
R 6h, alkyl, particularly methyl containing 1 ~ 20 carbon atom, ethyl, propyl group, butyl and hexyl, R 7~ R 9containing the alkyl, particularly methyl of 1 ~ 6 carbon atom, ethyl, propyl group, butyl and hexyl independently of one another, and R 6, R 7, R 8and R 9each other can be identical or different;
R 10h, alkyl, particularly methyl containing 1 ~ 6 carbon atom, ethyl, propyl group, butyl and hexyl, R 11~ R 13containing the alkyl, particularly methyl of 1 ~ 6 carbon atom, ethyl, propyl group, butyl and hexyl independently of one another, and R 10, R 11, R 12and R 13each other can be identical or different;
R 14h, alkyl, particularly methyl containing 1 ~ 6 carbon atom, ethyl, propyl group, butyl and hexyl, R 15the alkyl containing 1 ~ 6 carbon atom, and R 14and R 15can be identical, also can be different; With
X -for bromine, chlorine, iodine, fluoroboric acid root, nitrate radical, hexafluoro-phosphate radical.
As the specific examples of preferred ion liquid, specifically mention following material: N-butylpyridinium Chloride, chlorination N-methyl-N-butyl pyrrolidine, chlorination N-methyl butyl piperidines, chlorination N-methyl butyl morpholine, butyl trimethyl ammonium chloride and tributyl hexyl bromide phosphine.
As ionic liquid mentioned in literary composition, be as known in the art, can be commercially available, also can be prepared by currently known methods.
The present inventor is surprised to find that the solidification value using ionic liquid physical efficiency to reduce benzoxazine colophony, concrete reason for this reason it be unclear that, but infer it may is based on following reason: saturation type ionic liquid joins can by positively charged ion ring open mechanism in benzoxazine colophony, the ring-opening polymerization of catalysis benzoxazine colophony, makes the solidification value of benzoxazine colophony reduce and solidification is more complete.
But, above-mentioned reason is only predictive, and mechanism of the present invention is not limited thereto.
benzoxazine colophony
In this article, term used " benzoxazine colophony " refers to the compound of the benzoxazinyl group containing benzoxazinyl group shown in following formula or replacement in molecular structure, polymkeric substance or their mixture,
Wherein, R can be hydrogen, alkyl, aryl, unsaturated alkyl (as thiazolinyl), alicyclic radical or other organic groups (as alkyl silyl, itrile group, hydroxyl, carboxyl, haloalkyl, halogen atom, ether, thioether group, carbonyl, sulfuryl etc.).
In benzoxazine resin/ionic liquid compositions according to the present invention, benzoxazine colophony used is all known benzoxazine colophonies, not special requirement.
In preferred embodiments, described benzoxazine colophony refers to benzoxazine colophony, benzoxazine intermediate and their mixture containing structural unit one of at least in following (1)-(6) in molecular structure:
Wherein, R 1~ R 5be H independently of one another, alkyl, aryl, alicyclic radical, halogen atom (as chlorine, fluorine, bromine etc.), unsaturated alkyl (such as vinyl, allyl group etc.), trialkyl silyl, itrile group, hydroxyl, carboxyl etc. containing 1 ~ 20 carbon atom, and R 1~ R 5between each other can be identical, also can be different;
Wherein, n=2,3 or 4;
X is that alkylidene group is (as methylene radical, ethylidene, 2,2-propylidene, 2, the fluoro-propylidene of 2-6 etc.), arylidene, sub-alicyclic radical, ether, thioether group, carbonyl, sulfuryl, X (namely X is connecting key, and now this structural unit is xenyl benzoxazine unit) can not had yet;
R 1~ R 4be H independently of one another, alkyl, aryl, alicyclic radical, unsaturated alkyl (as vinyl, allyl group etc.), trialkyl silyl, itrile group, hydroxyl, carboxyl, haloalkyl or halogen atom (as chlorine, fluorine, bromine etc.) etc. containing 1 ~ 20 carbon atom, and R 1~ R 4between each other can be identical, also can be different;
Wherein, X is alkylidene group (as methylene radical, ethylidene, 2,2-propylidene, 2,2-6 fluoro-propylidene etc.), arylidene, sub-alicyclic radical, ether, thioether group, carbonyl, sulfuryl, and oligopolymer group;
R 1~ R 8be H independently of one another, the alkyl containing 1 ~ 20 carbon atom, haloalkyl, aryl, alicyclic radical, unsaturated alkyl (as vinyl, allyl group), trialkyl silyl, itrile group, hydroxyl, carboxyl or halogen atom (as chlorine, fluorine, bromine) etc., and R 1~ R 8between each other can be identical, also can be different;
Wherein, R 1~ R 3be H, alkyl (as methyl etc.), aryl, alicyclic radical etc. independently of one another;
R 4for H, alkyl, aryl, alicyclic radical, unsaturated alkyl (as vinyl, allyl group etc.), trialkyl silyl, itrile group, hydroxyl, carboxyl, haloalkyl or halogen atom (as chlorine, fluorine, bromine) etc. containing 1 ~ 20 carbon atom;
Wherein, R 1~ R 3be H, alkyl (as methyl etc.), aryl, alicyclic radical etc. independently of one another;
R 4~ R 7be H independently of one another, alkyl, aryl, alicyclic radical, unsaturated alkyl (as vinyl, allyl group etc.), trialkyl silyl, itrile group, hydroxyl, carboxyl, haloalkyl or halogen atom (as chlorine, fluorine, bromine) etc. containing 1 ~ 20 carbon atom;
Wherein, R 1, R 2be alkylidene group (as methylene radical), arylidene, sub-alicyclic radical, ether, thioether group, carbonyl, sulfuryl etc. independently of one another;
R 3for H, alkyl, aryl, alicyclic radical, unsaturated alkyl (as vinyl, allyl group etc.), trialkyl silyl, itrile group, hydroxyl, carboxyl, haloalkyl or halogen atom (as chlorine, fluorine, bromine) etc. containing 1 ~ 20 carbon atom.
Described preferred benzoxazine colophony is known, see such as with Publication about Document:
1, striking peak, Cheng Yanren. the progress [J] of ring-opening polymerization resol-benzoxazine colophony intermediate. thermosetting resin, 1998,3:39-42
2、Schreiber H.Computer-controlled drawing of stereographic projections of Kossel-lines and its uses in the study of tetragonal aberrations[P].Germany Patent，PN：2255504，1973
3, Li Shengfang, Fu Jifang, Wang Luoli. the progress [J] of benzoxazine colophony. Speciality Petrochemicals is in progress, 2004,8,47-48
4, Shi Zixing, Wang Yizhong, Yu Dingsheng. non-isothermal DSC method is to poly-two 3, the research [J] of 4-dihydro-3-phenyl-1,3-benzoxazine monomer curing action. About Frp/cm, 2000,2:14-17 or can be prepared by currently known methods, for example, see with Publication about Document:
1, Shi Zixing, Pan Ying, Wang Yizhong, etc. the structure of Polybenzoxazine performed polymer and the research [J] of curing action. Beijing University of Chemical Technology's journal, 2000,3:13-16
2、Shi Z X，Yu D S，Wang Y Z，et al.Investigation of isothermal curing behavior during the synthesis of polybenzoxazine-layered silicate nanocomposites via cyclic monomer[J].Euro.Polym.，2002，38(4)：727-733
In benzoxazine resin/ionic liquid compositions according to the present invention, except above-mentioned preferred benzoxazine colophony, benzoxazine colophony can also optionally comprise in following benzoxazine one or more: N-alkyl benzoxazine colophony, N-Fang base benzoxazine colophony, N-alicyclic radical benzoxazine colophony, N-unsaturated group benzoxazine colophony, benzoxazine colophony raw material based on phenolphthalein comes from the benzoxazine colophony of renewable resources, such as based on decamethylene diamine, butanediamine, chaff amine, cardanol, methyl catechol, the benzoxazine colophony of Eugenol etc., containing dimaleoyl imino, the benzoxazine colophony of Na Dike imide.These benzoxazine colophonies are known, or can be prepared by currently known methods.
In benzoxazine resin/ionic liquid compositions according to the present invention, benzoxazine colophony optionally can also comprise the benzoxazine colophony containing polyhedral oligomeric silsesquioxane.
In benzoxazine resin/ionic liquid compositions according to the present invention, benzoxazine colophony can also optionally comprise backbone chain type benzoxazine colophony, and such as reference is with Publication about Document:.
1、Kiskan B，Yagci Y，Ishida H.Synthesis，characterization，and properties of new thermally curable polyetheresters containing benzoxazinemoieties in the main chain[J].J.App l.Polym.Sci，2008，46(2)：414-420
2、Kiskan B，Koz，B Yagci Y.Synthesis and Characterization of Fluid1，3-Benzoxazine Monomers and Their Thermally Activated Curing[J].J.Appl.Polym.Sci，2009，47，6955-6961
3、Tuzun A，Kiskan B，N A，Erciyes A T，Yagici Y.Benzoxazine containing polyester thermosets with improved adhesion and flexibility[J].JAppl.Polym.Sci，2010，48(19)：4279-4284
4, Xu Wei, Zhang Pengli, Liang Peiyin, etc. benzoxazine colophony of alcoholic hydroxy and preparation method thereof [P] .CN, 201010296172.X, 2010
the preparation method of benzoxazine resin/ionic liquid compositions
According to a further aspect in the invention, provide the preparation of benzoxazine resin/ionic liquid compositions, the method realizes by being mixed with ionic liquid by benzoxazine colophony.
As hybrid mode, hybrid mode well-known to those skilled in the art can be used, as mechanical stirring mixing, solution mixing, melting mixing, assisting ultrasonic dispersion, high-speed stirring etc.
thermosetting resin resin combination
In accordance with a further aspect of the present invention, provide compositions of thermosetting resin, it comprises: according to benzoxazine resin/ionic liquid compositions of the present invention, and other thermosetting resins and/or filler.
As other thermosetting resins described, benzoxazine colophony such as N-alkyl benzoxazine colophony, N-benzene base benzoxazine colophony, N-alicyclic radical benzoxazine colophony, N-allyl group benzoxazine colophony etc. can be used, epoxy resin, unsaturated polyester resin, Vinylite, bimaleimide resin, resol, urethane resin, cyanate ester resin, Thermocurable polyimide, aryl ethane resin or furane resin etc.According to the object expected and purposes, select that there is various thermosetting resin of different nature.This is in the limit of power of those skilled in the art.
As filler, the various strongtheners that those skilled in the art are familiar with can be used, comprise inorganic reinforcement such as silicon-dioxide, calcium carbonate, carbon nanotube, carbon fiber etc., organic reinforcing as aramid fiber etc., hybrid reinforcement material such as polyhedral silsesquioxane etc.According to the object expected and purposes, the filler that choice for use is concrete, this is in the limit of power of those skilled in the art.
Benzoxazine resin/ionic liquid compositions provided by the invention or compositions of thermosetting resin shapingly by common thermosetting resin complete processing can make cured article, as sprayup process, resin transfer molding technology (RTM technology), compression molding technology, pouring forming technology, impregnation technology, winding process, pultrusion molding process etc.The porosity of resulting product or matrix material is low, shrinks little; Can High-performance adhesive and coating be used as, as the matrix resin of high performance composite, and traditional resol, epoxy resin can be replaced for electronic industry.
embodiment
Below by way of specific embodiment, the present invention is described further, but these embodiments are only exemplary, should not be construed as limitation of the scope of the invention.
Embodiment 1
Ratio (mass ratio) with 0.1: 99.9 prepares N-butylpyridinium Chloride ionic liquid and dihydroxyphenyl propane aniline type benzoxazine colophony (preparation method: add solvent toluene 500ml successively in the 1000ml there-necked flask having prolong, stirring and thermometer, add dihydroxyphenyl propane 114g (0.5mol), aniline 120ml (1mol) successively, paraformaldehyde 60g (2mol) is slowly added under violent stirring in ice-water bath, violent stirring under room temperature, reactant is mixed, is placed in 105 DEG C of oil baths and reacts 4h.The alkali lye adding 1mol/L after reaction terminates is uniformly mixed, then pour in separating funnel and isolate product, continuation alkali lye is washed, finally be washed till neutrality with deionized water, pour 60 DEG C of vacuum-drying 24h in porcelain dish into, obtain flaxen solid and dihydroxyphenyl propane aniline type benzoxazine) composition, compound method is by adopting the mode of solution mixing ultrasonic disperse, get ionic liquid and bisphenol A benzoxazine is dissolved in chloroform, ultrasonic disperse 10min, allow chloroform solvent vapor away under room temperature, obtain benzoxazine resin/ionic liquid compositions.
Composition is carried out DSC test (see test example), gained DSC curve is shown in (please supplement complete DSC curve) shown in Fig. 1.Record that curing initiation temperature is 224 DEG C, cure peak temperature be 237 DEG C and solidification final temperature is 254 DEG C.
Embodiment 2
In the same manner as in the example 1, the composition of N-methyl-N-butyl pyrrolidine chloride salt ions liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 0.1: 99.9.
Composition carries out DSC test, and gained DSC curve is shown in (please supplement complete DSC curve) shown in Fig. 2, records that curing initiation temperature is 206 DEG C, cure peak temperature be 229 DEG C and solidification final temperature is 256 DEG C.
Embodiment 3
In the same manner as in the example 1, the composition of N-methyl-N-butyl piperidine chloride salt ions liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 0.1: 99.9.
Composition carries out DSC test, and gained DSC curve is shown in (please supplement complete DSC curve) shown in Fig. 3, records that curing initiation temperature is 202 DEG C, cure peak temperature be 223 DEG C and solidification final temperature is 259 DEG C.
Embodiment 4
In the same manner as in the example 1, the composition of butyl Trimethylamine ionic liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 0.1: 99.9.
Composition carries out DSC test, and gained DSC curve is shown in (please supplement complete DSC curve) shown in Fig. 4, records that curing initiation temperature is 201 DEG C, cure peak temperature be 223 DEG C and solidification final temperature is 260 DEG C.
Embodiment 5
In the same manner as in the example 1, the composition of tributyl hexyl bromide phosphine ionic liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 0.1: 99.9.
Composition carries out DSC test, and gained DSC curve is shown in (please supplement complete DSC curve) shown in Fig. 5, records that curing initiation temperature is 213 DEG C, cure peak temperature be 230 DEG C and solidification final temperature is 251 DEG C.
Embodiment 6
In the same manner as in the example 1, the composition of N-methyl-N-butyl pyrrolidine chloride salt ions liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 0.2: 99.8.
Composition carries out DSC test, records that curing initiation temperature is 200 DEG C, cure peak temperature be 223 DEG C and solidification final temperature is 257 DEG C.
Embodiment 7
In the same manner as in the example 1, the composition of N-methyl-N-butyl piperidine chloride salt ions liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 0.2: 99.8.
Composition carries out DSC test, records that curing initiation temperature is 202 DEG C, cure peak temperature be 223 DEG C and solidification final temperature is 258 DEG C.
Embodiment 8
In the same manner as in the example 1, the composition of butyl Trimethylamine ionic liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 0.2: 99.8.
Composition carries out DS C test, records that curing initiation temperature is 194 DEG C, cure peak temperature be 219 DEG C and solidification final temperature is 262 DEG C.
Embodiment 9
In the same manner as in the example 1, the composition of tributyl hexyl bromide phosphine ionic liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 0.2: 99.8.
Composition carries out DSC test, records that curing initiation temperature is 207 DEG C, cure peak temperature be 226 DEG C and solidification final temperature is 251 DEG C.
Embodiment 10
In the same manner as in the example 1, the composition of N-methyl-N-butyl pyrrolidine chloride salt ions liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 0.5: 99.5.
Composition carries out DSC test, records that curing initiation temperature is 194 DEG C, cure peak temperature be 220 DEG C and solidification final temperature is 256 DEG C.
Embodiment 11
In the same manner as in the example 1, the composition of N-methyl-N-butyl piperidine chloride salt ions liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 0.5: 99.5.
Composition carries out DSC test, records that curing initiation temperature is 195 DEG C, cure peak temperature be 219 DEG C and solidification final temperature is 265 DEG C.
Embodiment 12
In the same manner as in the example 1, the composition of butyl Trimethylamine ionic liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 0.5: 99.5.
Composition carries out DSC test, records that curing initiation temperature is 195 DEG C, cure peak temperature be 221 DEG C and solidification final temperature is 264 DEG C.
Embodiment 13
In the same manner as in the example 1, the composition of tributyl hexyl bromide phosphine and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 0.5: 99.5.
Composition carries out DS C test, records that curing initiation temperature is 206 DEG C, cure peak temperature be 225 DEG C and solidification final temperature is 251 DEG C.
Embodiment 14
In the same manner as in the example 1, the composition of N-butylpyridinium Chloride ionic liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 1.0: 99.0.
Composition carries out DSC test, records that curing initiation temperature is 203 DEG C, cure peak temperature be 225 DEG C and solidification final temperature is 254 DEG C.
Embodiment 15
In the same manner as in the example 1, the composition of N-methyl-N-butyl pyrrolidine chloride salt ions liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 1.0: 99.0.
Composition carries out DSC test, records that curing initiation temperature is 205 DEG C, cure peak temperature be 225 DEG C and solidification final temperature is 246 DEG C.
Embodiment 16
In the same manner as in the example 1, prepare with the ratio (mass ratio) of 1.0: 99.0 oil/fat composition that N-methyl-N-butyl piperidine chloride salt ions liquid and dihydroxyphenyl propane aniline type benzoxazine set.
Composition carries out DSC test, records that curing initiation temperature is 197 DEG C, cure peak temperature be 218 DEG C and solidification final temperature is 265 DEG C.
Embodiment 17
In the same manner as in the example 1, prepare with the ratio (mass ratio) of 1.0: 99.0 oil/fat composition that butyl Trimethylamine ionic liquid and dihydroxyphenyl propane aniline type benzoxazine set.
Composition carries out DS C test, records that curing initiation temperature is 192 DEG C, cure peak temperature be 218 DEG C and solidification final temperature is 260 DEG C.
Embodiment 18
In the same manner as in the example 1, the composition of tributyl hexyl bromide phosphine and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 1.0: 99.0.
Composition carries out DSC test, records that curing initiation temperature is 216 DEG C, cure peak temperature be 232 DEG C and solidification final temperature is 250 DEG C.
Embodiment 19
In the same manner as in the example 1, the composition of N-methyl-N-butyl pyrrolidine chloride salt ions liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 2.0: 98.0.
Composition carries out DSC test, records that curing initiation temperature is 198 DEG C, cure peak temperature be 224 DEG C and solidification final temperature is 251 DEG C.
Embodiment 20
In the same manner as in the example 1, the composition of N-methyl-N-butyl piperidine chloride salt ions liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 2.0: 98.0.
Composition carries out DSC test, records that curing initiation temperature is 191 DEG C, cure peak temperature be 218 DEG C and solidification final temperature is 256 DEG C.
Embodiment 21
In the same manner as in the example 1, the composition of butyl Trimethylamine ionic liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 2.0: 98.0.
Composition carries out DSC test, records that curing initiation temperature is 184 DEG C, cure peak temperature be 221 DEG C and solidification final temperature is 258 DEG C.
Embodiment 22
In the same manner as in the example 1, the composition of tributyl hexyl bromide phosphine and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 2.0: 98.0.
Composition carries out DSC test, records that curing initiation temperature is 213 DEG C, cure peak temperature be 229 DEG C and solidification final temperature is 250 DEG C.
Embodiment 23
In the same manner as in the example 1, the composition of N-butylpyridinium Chloride ionic liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 5.0: 95.0.
Composition carries out DSC test, records that curing initiation temperature is 197 DEG C, cure peak temperature be 224 DEG C and solidification final temperature is 254 DEG C.
Embodiment 24
In the same manner as in the example 1, the composition of N-methyl-N-butyl pyrrolidine chloride salt ions liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 5.0: 95.0.
Composition carries out DSC test, records that curing initiation temperature is 198 DEG C, cure peak temperature be 227 DEG C and solidification final temperature is 252 DEG C.
Embodiment 25
In the same manner as in the example 1, the composition of N-methyl-N-butyl piperidine chloride salt ions liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 5.0: 95.0.
Composition carries out DSC test, records that curing initiation temperature is 190 DEG C, cure peak temperature be 221 DEG C and solidification final temperature is 255 DEG C.
Embodiment 26
In the same manner as in the example 1, the composition of butyl Trimethylamine ionic liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 5.0: 95.0.
Composition carries out DSC test, records that curing initiation temperature is 183 DEG C, cure peak temperature be 223 DEG C and solidification final temperature is 256 DEG C.
Embodiment 27
In the same manner as in the example 1, the composition of N-butylpyridinium Chloride ionic liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 10.0: 90.0.
Composition carries out DSC test, records that curing initiation temperature is 188 DEG C, cure peak temperature be 219 DEG C and solidification final temperature is 252 DEG C.
Embodiment 28
In the same manner as in the example 1, the composition of N-methyl-N-butyl pyrrolidine chloride salt ions liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 10.0: 90.0.
Composition carries out DSC test, records that curing initiation temperature is 194 DEG C, cure peak temperature be 226 DEG C and solidification final temperature is 249 DEG C.
Embodiment 29
In the same manner as in the example 1, the composition of N-methyl-N-butyl piperidine chloride salt ions liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 10.0: 90.0.
Composition carries out DSC test, records that curing initiation temperature is 186 DEG C, cure peak temperature be 223 DEG C and solidification final temperature is 263 DEG C.
Embodiment 30
In the same manner as in the example 1, the composition of butyl trimethyl ammonia chloride amine ionic liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 10.0: 90.0.
Composition carries out DSC test, records that curing initiation temperature is 186 DEG C, cure peak temperature be 223 DEG C and solidification final temperature is 258 DEG C.
Embodiment 31
In the same manner as in the example 1, the composition of N-butylpyridinium Chloride ionic liquid and dihydroxyphenyl propane aniline type benzoxazine colophony is prepared with the ratio (mass ratio) of 15.0: 85.0.
Composition carries out DSC test, records that curing initiation temperature is 189 DEG C, cure peak temperature be 222 DEG C and solidification final temperature is 253 DEG C.
Embodiment 32
In the same manner as in the example 1, ratio (mass ratio) with 1: 99 prepares N-butylpyridinium Chloride ionic liquid and p-cresol type benzoxazine colophony (p-cresol type benzoxazine colophony preparation method: solvent made by toluene, under room temperature in intense mechanical whipping process by p-cresol, aniline, paraformaldehyde joins in there-necked flask successively, to be mixed evenly after be warming up to 100 DEG C of reaction 4h, the alkali liquid washing that reaction terminates rear 1mol/L isolates product, then after being washed till neutrality with deionized water, pour 60 DEG C of vacuum-drying 24h in porcelain dish into, obtain yellowish solid) composition.
Composition carries out DSC test, records that curing initiation temperature is 250 DEG C, cure peak temperature be 259 DEG C and solidification final temperature is 267 DEG C.
Comparative example 1
Dihydroxyphenyl propane aniline type benzoxazine colophony is ground, obtain pale yellow powder, DSC test (see following test example) is carried out to pale yellow powder, gained DSC curve is shown in shown in Fig. 6, records that its curing initiation temperature is 244 DEG C, cure peak temperature be 252 DEG C and solidification final temperature is 260 DEG C.
Comparative example 2
By the p-cresol type benzoxazine colophony grinding used in embodiment 32, DSC test (see following test example) is carried out to it, gained DSC curve is shown in shown in Fig. 7, record its curing initiation temperature be respectively 260 DEG C, cure peak temperature be respectively 266 DEG C and solidification final temperature be respectively 273 DEG C.
Embodiment 1-31 and comparative example 1, embodiment 32 are compared known with comparative example 2, when using ionic liquid, the curing initiation temperature of benzoxazine colophony all significantly reduces with solidification final temperature, when ionic liquid consumption is lower, the cure peak temperature of benzoxazine colophony also obviously reduces.
test example DSC tests
Perkin-Elmer Pyris1 type DSC is adopted to test, test condition: N 2environment, temperature rise rate is 10 DEG C/min, Al 2o 3for reference substance, Range of measuring temp is room temperature ~ 350 DEG C.

Claims (7)

1. benzoxazine resin/ionic liquid compositions, wherein the mass ratio of ionic liquid and benzoxazine colophony is 0.1 ~ 50:99.9 ~ 50,
Described benzoxazine colophony refers to the benzoxazine colophony containing structural unit one of at least in following formula (1) and (2) in molecular structure:
Wherein, R 1~ R 5be H, the alkyl containing 1 ~ 20 carbon atom, aryl independently of one another;
Wherein, n=2;
X is 2,2-propylidene;
R 1~ R 4be H, the alkyl containing 1 ~ 20 carbon atom, aryl independently of one another;
The ionic liquid of described ionic liquid to be organic cation side chain be saturated alkyl, be selected from following in one or more:
Wherein, R 1methyl, ethyl, propyl group, butyl and hexyl;
R 4h, methyl, ethyl, propyl group, butyl and hexyl, R 5methyl, ethyl, propyl group, butyl and hexyl, and R 4and R 5can be identical, also can be different;
R 6h, methyl, ethyl, propyl group, butyl and hexyl, R 7~ R 9methyl, ethyl, propyl group, butyl and hexyl independently of one another, and R 6, R 7, R 8and R 9each other can be identical or different;
R 10h, methyl, ethyl, propyl group, butyl and hexyl, R 11~ R 13methyl, ethyl, propyl group, butyl and hexyl independently of one another, and R 10, R 11, R 12and R 13each other can be identical or different;
With
X -for chlorine.
2. benzoxazine resin/ionic liquid compositions according to claim 1, wherein the mass ratio of ionic liquid and benzoxazine colophony is 0.1 ~ 20:99.9 ~ 80.
3. benzoxazine resin/ionic liquid compositions according to claim 2, wherein the mass ratio of ionic liquid and benzoxazine colophony is 0.1 ~ 5:99.9 ~ 95.
4. the benzoxazine resin/ionic liquid compositions according to any one of claim 1-3, wherein, described ionic liquid be following in one or more: N-butylpyridinium Chloride, chlorination N-methyl butyl piperidines and butyl trimethyl ammonium chloride.
5. compositions of thermosetting resin, it comprises: the benzoxazine resin/ionic liquid compositions according to any one of claim 1-4, and other thermosetting resins and/or filler, wherein as other thermosetting resins described, use following in one or more: benzoxazine colophonies, epoxy resin, unsaturated polyester resin, Vinylite, bimaleimide resin, resol, urethane resin, cyanate ester resin, Thermocurable polyimide, aryl ethane resin or furane resin
Wherein as filler, use following in one or more: inorganic reinforcement, organic reinforcing, hybrid reinforcement material.
6. compositions of thermosetting resin according to claim 5, wherein said benzoxazine colophony is N-alkyl benzoxazine colophony, N-benzene base benzoxazine colophony, N-alicyclic radical benzoxazine colophony, N-allyl group benzoxazine colophony.
7. compositions of thermosetting resin according to claim 5, wherein said inorganic reinforcement is silicon-dioxide, calcium carbonate, carbon nanotube, carbon fiber, and described organic reinforcing is aramid fiber, and described hybrid reinforcement material is polyhedral silsesquioxane.
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