• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
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  • 优先权
    • 专利摘要:
    The present invention relates to the use of bis-anhydrohexitol ethers as reactive diluents in a crosslinkable composition of resin, adhesive, coating or matrix for composites. Not only can these products advantageously reduce the viscosity of the mixtures obtained, but they also lead to a very small decrease in the glass transition temperature of the crosslinked mixtures, compared with other reactive diluents and while dramatically improving the mechanical properties. of these, such as Young's modulus, tensile strength, elongation at break, and toughness.
    公开号:FR3040059A1
    申请号:FR1557712
    申请日:2015-08-13
    公开日:2017-02-17
    发明作者:Clothilde Buffe；Jean Pierre Pascault；Meizoso Loureiro Roi；Gonzales Pilar Prendes；Abuin Senen Paz
    申请人:Roquette Freres SA；
    IPC主号:
    专利说明:

    USE OF A LOW VISCOSITY BIS-ANHYDROHEXITOL ETHERS COMPOSITION AS A REACTIVE DILUENT FOR RETICULABLE COMPOSITIONS OF RESINS, ADHESIVES, COATINGS AND MATRICES
    FOR COMPOSITES
    The present invention relates to the use of bis-anhydrohexitol ethers as reactive diluents for the preparation of a polymerizable and / or crosslinkable composition of resin, adhesive, coating or matrix for composites. Not only can these products advantageously reduce the viscosity of the mixtures obtained, but they also lead to a very small decrease in the glass transition temperature of the crosslinked mixtures, compared with other reactive diluents and while dramatically improving the mechanical properties. of these, such as Young's modulus, tensile strength, elongation at break, and toughness.
    Reactive diluents are products or product mixtures having a relatively high boiling point (or a low saturated vapor pressure) and a relatively low viscosity. In general, reference is made to a threshold value of 500 mPa.s for their Brookfield viscosity as measured at 25 ° C, as indicated in the article "19.1Diluents" of the Ullmann encyclopedia (Pham, Ha Q. and Marks, Maurice J., Epoxy Resins, In Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH Verlag GmbH & Co. KGaA: 2000). The range of reactive diluents sold by Huntsmann under the name Araldite® illustrates this value in particular (see the brochure: "Advanced Materials - High Performance Components - Huntsmann, Section 7).
    The reactive diluents act as solvents during the manufacture and forming of multiple polymerizable and / or crosslinkable compositions for the manufacture of eg resin, adhesives, various coatings such as paints, lacquers, varnishes , or matrices for composites. With respect to said solvents, they have the advantage of not evaporating or migrating, since they participate in the development of the three-dimensional network. In the case of polymerizable and / or crosslinkable compositions based on epoxy resin, their primary function is to reduce the viscosity of said resin, thus improving its "machinability". This machinability refers to the ability of the resin to be used to make crosslinkable compositions sometimes complex, since based on many other additives such as fillers, pigments, biocides, defoamers, etc ... L state of the art is very rich on reactive diluents, especially for polymerizable organic matrices of the epoxy type or epoxy resins. Reference may be made in particular to the Huntsman company brochure discussed above. The Araldite® range is available through numerous products, such as those based on butanediol diglycidyl ether (Araldite® DY 026), alkyl (C12-C14) glycidyl ether (Araldite® DY-E) or trimethylolpropane triglycidyl ether (Araldite® DY-T).
    However, while seeking to ensure an excellent level of performance reactive diluents it manufactures, the skilled person must now incorporate new constraints including environmental. The development of polymeric materials derived from renewable resources in the short term has indeed become a major ecological and economic imperative, faced with the depletion and rising prices of fossil resources such as oil. In this context, the use of dianhydrohexitols, derived from vegetable (poly) saccharides, appears promising to replace monomers of petrochemical origin.
    In such a context, the applicant company has succeeded in identifying products which satisfy these environmental constraints, and which, quite surprisingly, behave as excellent reactive diluents for polymerizable and / or crosslinkable compositions, especially those based on resin. epoxy, advantageously decreasing the Brookfield viscosity of said compositions.
    In addition, unlike conventional reactive diluents, the products whose use is the subject of the present invention can very modestly reduce the glass transition temperature of the polymerized compositions and / or crosslinked. In fact, conventional reactive diluents have the major disadvantage of plasticizing the polymerized and / or crosslinked composition and thereby decreasing the glass transition temperature of said composition.
    The products whose use is the subject of the present invention also make it possible to improve the mechanical properties and in particular the impact resistance of the polymerized or crosslinked compositions. This is all the more surprising and advantageous since it is well known that reactive diluents can negatively impact these properties, as pointed out in the document "Ullman encyclopedia of industrial chemistry" (Pham, Ha Q. and Marks, Maurice J. Epoxy Resins In Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH Verlag GmbH & Co. KGaA: 2000) already discussed.
    As demonstrated by the examples that support the present application, the level of performance achieved for the mechanical properties and in particular the impact resistance of the polymerized and / or crosslinked compositions containing the products whose use is the subject of the present invention is well higher than that obtained with commercial reagent diluents, such as butanediol diglycidyl ether, (C 12 -C 14) alkyl glycidyl ether or trimethylolpropane triglycidyl ether.
    The products in question, the use of which is the subject of the present invention, which are already known, consist of bis-anhydrohexitol ethers of formula (I):
    (I) and having a Brookfield viscosity measured at 20 ° C of less than 500 mPa.s.
    Regardless of their viscosity, these products are today widely known and described in the literature, as well as their synthesis process. Nevertheless, it had never been envisaged or suggested to use such products as reactive diluents.
    One of the known processes for their synthesis is based on the initial formation of a solution of an isohexide salt in the presence of highly reactive species such as sodium hydride or sodium metal, and then on the reaction with epichlorohydrin. US 3,272,845 is an illustration thereof.
    US 4,770,871 proposes an alternative method which avoids the use of metal hydride or sodium metal. This method involves reacting a bis-anhydrohexitol and an alkyl carbonate in the presence of a basic catalyst, and under conditions of elevated temperature and pressure (200 to 300 ° C, 5 MPa).
    Document WO 2008/147472 is also known which describes another process which does not implement the abovementioned dangerous compounds. This document proposes a method of synthesis by dissolving an isohexitol in a solvent, adding a base, conducting azeotropic distillation with the solvent, adding a compound chosen from the group consisting of a halide of alkyl or aralkyl, and a sulfonate ester of the alcohol equivalent to the alkoxide, and heating to effect the etherification reaction and obtain the desired product.
    US Pat. No. 3,041,300 proposes a process consisting of reacting isosorbide and epichlorohydrin at atmospheric pressure with hot (about 110 ° C.), and adding very slowly a basic reagent such as sodium hydroxide solution (for at least 4 hours), and to carry out azeotropic distillation. After filtration and rinsing, the bis-anhydrohexitol ether thus formed is then recovered.
    More recently, WO 2012/157832 has proposed a variant of this technique, this time achieving the reaction between isosorbide and epichlorohydrin always under atmospheric pressure but at a more moderate temperature (40 ° C).
    Finally, the document WO 2008/147473 describes 3 preceding methods: in its example 1, the method based on azeotropic distillation in the presence of solvent according to the document WO 2008/147472, in its example 2, the method using hydride of sodium according to US 3,272,845, in Example 4, the method based on the very slow addition of sodium hydroxide and the azeotropic distillation according to US 3,041,300 and WO 2012/157832.
    This document WO 2008/147473 teaches another route which is a two-step process, the first consisting of reacting isohexitol with epichlorohydrin in the presence of boron trifluoride and then adding an alkaline solution (example 3 of this document ).
    Also known is the document WO 2013/188253, which describes a method consisting in: reacting a stereoisomer of isohexide with a Bronsted base whose conjugated acid has a pKa greater than 16, reacting the resulting product with a bromide of alkylate the resulting product with at least 2 molar equivalents of meta-chloroperbenzoic acid.
    The plaintiff company has itself protected an original method of manufacturing these products in the patent application FR 3,016,631, said process comprising the following steps: a) contacting a dianhydrohexitol and an organic halide, b) placing the mixture thus obtained dianhydrohexitol and organic halide under vacuum so as to obtain a depression of between 100 mbar and 1000 mbar, c) heating the mixture under vacuum at a temperature between 50 ° C and 120 ° C and thus achieve azeotropic distillation d) subsequently adding to said mixture a basic reagent for a period of between 1 hour and 10 hours and then continuing the azeotropic distillation, e) recovering the composition of bis-anhydrohexitol ethers after a filtration step, concentration of the filtrate and optionally a purification step.
    This process has the advantage of being both free of solvents and other potentially hazardous compounds such as metal hydride, sodium metal, or boron trifluoride.
    The present invention is in no way limited by the process for obtaining the composition of bis-anhydrohexitol ethers of formula (I). It should be noted that all of the aforementioned methods actually lead to mixtures of compounds of formula (II) whose viscosity is a function in particular of the presence and amount of oligomers. As such, if the composition obtained did not immediately have the characteristic required in terms of viscosity (Brookfield viscosity less than 500 mPa.s at 20 ° C), the skilled person would then be able to apply a subsequent treatment (such as a distillation) in order to eliminate enough oligomeric species, and thus reduce the viscosity of the medium.
    (II) In this respect, and according to a preferred variant, the bis-anhydrohexitol ether of formula (I) is that obtained by the process described in the aforementioned patent application FR 3,016,631, with implementation of the purification step (in step e)) in the form of a fractionation step, such as in particular carried out by distillation.
    There is no suggestion to implement such a fractionation step and more particularly a distillation step in the aforementioned application, in order to obtain an effective reactive diluent. A fortiori, nothing also disclosed or incited to conduct this distillation step so as to aim for a Brookfield viscosity less than 500 mPa.s at 20 ° C. But what is still most surprising is that such a product is even more efficient than the best reactive diluents on the market, which are those exemplified in the present application and described above, especially under non-commercial terms and trademarks. only well known to those skilled in the art but also the general public as Araldite®. In this respect, the products whose use is the subject of the present invention make it possible to obtain polymerized and / or crosslinked materials having a compromise that has never been equaled in terms of mechanical properties and the maintenance of the transition temperature. glass. It is recalled in this respect that the products used as comparative in the patent application FR 3,016,631 were other than products "identical" from a chemical point of view, but obtained by different processes and therefore, not known as reactive diluents and therefore much less discriminating in this respect.
    Another element of surprise lies in the "intrinsic" Brookfield viscosity of the products whose use is the subject of the present invention. This viscosity is much higher than that of the reactive diluents of the prior art (as indicated in Table 1 below). It is perfectly surprising to obtain a compromise never before equated between mechanical properties and glass transition temperature, whereas the general education would consist in reducing as much as possible the viscosity of a reactive diluent in order to obtain such a performance.
    Also, a first object of the present invention is the use, as a reactive diluent for the preparation of a polymerizable and / or crosslinkable composition of resin, adhesive, coating, or composite matrix, of at least a bis-anhydrohexitol ether of formula (I):
    (I) and having a Brookfield viscosity, measured at 20 ° C of less than 500 mPa.s.
    This use is also characterized in that the compound of formula (I) has a Brookfield viscosity, preferably less than 400 mPa.s, very preferably less than 300 mPa.s and even more preferentially between 50 and 300 mPa.s, and most preferred of all between 100 and 300 mPa.s.
    The "reactive diluent" function in the present application covers the ability of the product in question to lower the viscosity of the polymerizable and / or crosslinkable composition in which it is intended to be incorporated.
    This use is also characterized in that the compound of formula (I) has an epoxy equivalent by weight of between 129 and 145 g / eq, preferably between 129 and 136 g / eq. This equivalent is measured according to ISO 3001 or ASTM D1652.
    This use is also characterized in that the compound of formula (I) has a chlorine content by mass of less than 0.5%, preferably less than 0.3%. This content is measured according to ISO 21627-3.
    In a preferred manner, this use is characterized in that said crosslinkable and / or polymerizable composition is based on an epoxy-type polymerizable organic matrix. We can then speak of composition based on epoxy resin.
    Most of the polymerizable and / or crosslinkable compositions used in particular for the manufacture of resin, adhesive, coating or matrix of composites are complex products for which the processing methods and the final properties are adapted to the customer's needs by the formulators' skills.
    In the case of polymerizable and / or crosslinkable compositions based on polymerizable organic matrix of the epoxy type, these compositions contain, in addition to said polymerizable organic matrix, at least one hardener and / or an accelerator.
    The crosslinking may be carried out at ambient temperature or at elevated temperature (above 100 ° C.) and / or under radiation (UV or electron scanning) by cationic crosslinking.
    By accelerator is meant compounds for catalyzing the homopolymerization reaction between the epoxy functions or between the epoxy functions and the accelerating agent. Lewis acids, Lewis bases and photoinitiators are examples.
    By hardener means any compound for forming a three-dimensional network by reaction with the epoxy functions. Amines, amidoamines, Mannich bases, organic or anhydride acids, latent hardeners (dicyandiamide type, imidazole, etc.), and carboxyl-terminated polyesters are examples thereof.
    In the case of single-component systems, accelerators and / or hardeners are directly incorporated into the resin: this is known as the 1K system. While in two-component systems (2K), the curing agent and / or curing agent is formulated separately and mixing occurs only at the time of application and shaping of the resin.
    The polymerizable and / or crosslinkable compositions may also contain organic or inorganic fillers (silica, sand, aluminum oxide, talc, calcium carbonate, etc.), pigments, plasticizers, stabilizers or thixotropic agents.
    The viscosity of certain polymerizable and / or crosslinkable compositions based on an epoxy-type polymerizable organic matrix being too high to form diluents are used in order to improve the machinability of the compositions. The implementation and the shaping of polymerizable and / or crosslinkable compositions based on polymerizable organic matrix of epoxy or epoxy resin type are then facilitated as well as the dispersion of the additives or fillers.
    Among the constituents of epoxy resins include glycidyl ether Bisphenol A (DGEBA), novolac resins (phenol or cresol type), epoxy resins bisphenol F base, cycloaliphatic epoxy resins, brominated epoxy resins ... As a For example, the standard grades of DGEBA liquid resins have a viscosity of between 10,000 and 15,000 mPa.s at 25 ° C (DER 331, EPON 828) and the Novolak resins have a viscosity greater than 20,000 mPa.s (Araldite EPN 1138).
    The amount of reactive diluent added to the polymerizable and / or crosslinkable composition is adapted as a function of the final viscosity desired by the specification. Generally amounts of 5 to 50% by dry weight relative to the total weight (polymerizable composition, preferably based on epoxy resin and reactive diluent) are used. The reactive diluent is then added, preferably with mechanical stirring, to the polymerizable and / or crosslinkable composition in order to obtain a homogeneous mixture. The bis-anhydrohexitol ether is added to said polymerizable and / or crosslinkable composition by any of the techniques well known to those skilled in the art. The use of reactive diluent for the preparation of polymerizable and / or crosslinkable compositions allows the manufacture of composites by casting, coating, infusion, impregnation, lamination, injection, pultrusion, filament winding. The use of reactive diluent for the preparation of polymerizable and / or crosslinkable compositions also facilitates the deposition of thin layers, the use of a gun, a roller and the sufficient wettability of the supports or fibers.
    The fields of application of the present invention are in particular those of building and civil engineering (flooring, concrete), the repair or manufacture of composites, adhesives, inks, paints, electronics (coating of thermoplastic housings, coating of printed circuits).
    Another object of the present invention is a polymerizable and / or crosslinkable resin, adhesive, coating or composite matrix composition, said composition comprising: a polymerizable and / or crosslinkable organic matrix; at least one bis-anhydrohexitol ether of formula (I):
    (I) - and having a Brookfield viscosity, measured at 20 ° C, of less than 500 mPa.s.
    This polymerizable and / or crosslinkable composition is also characterized in that the compound of formula (I) has a Brookfield viscosity measured at 20 ° C. preferably less than 400 mPa.s, very preferably less than 300 mPa.s and even more preferentially between 50 and 300 mPa.s, and most preferably between 100 and 300 mPa.s.
    This polymerizable and / or crosslinkable composition is also characterized in that the ether of formula (I) has an epoxy equivalent by weight of between 129 and 145 g / eq, preferably between 129 and 136 g / eq. This equivalent is measured according to ISO 3001 or ASTM D1652.
    This polymerizable and / or crosslinkable composition is also characterized in that the compound of formula (I) has a total chlorine content by mass of less than 0.5%, preferably less than 0.3%. This content is measured according to ISO 21627-3.
    This polymerizable and / or crosslinkable composition is also characterized in that the polymerizable and / or crosslinkable matrix is of the epoxy or epoxy resin type.
    The polymerizable and / or crosslinkable composition according to the present invention may comprise at least one hardener and / or an accelerator.
    In the case where the polymerizable organic matrix is an epoxy resin, the crosslinkable and / or polymerizable composition further comprises at least one hardener and / or an accelerator.
    Another subject of the present invention is the crosslinked and / or polymerized composition obtained by crosslinking and / or polymerizing the composition as defined above.
    The following examples make it possible to better understand the content of the present invention, without however limiting its scope.
    EXAMPLES
    The following examples relate to the use of different reactive diluents according to the invention (diglycidyl ether of isosorbide) or according to the prior art (commercial products) in a crosslinkable composition based on polymerizable organic matrix of the epoxy type or to epoxy resin base.
    Preparation of diglycidyl ether of isosorbide:
    It is introduced into a 1 liter jacketed reactor, heated by a heat transfer fluidized bath equipped with a mechanical stirring system to a pale, a system for controlling the temperature of the reaction medium and a Dean Stark 125 g of isosorbide (0.86 mol, 1 molar equivalent), 395.6 g of epichlorohydrin (4.27 mol, 5 molar equivalents) followed by 1.25 g of triethylammonium bromide ( 1% by mass relative to isosorbide).
    The system is brought to a pressure of 275 mbar relative. The reaction mixture is heated to 80 ° C. (boiling temperature = 80 ° C. to 275 mbar) before starting the controlled addition of 136.9 g of a 50% aqueous solution of sodium hydroxide ( 1.71 mol, 2 molar equivalents). The addition lasts a total of 2 hours 50 minutes. The water is then removed continuously by azeotropic distillation.
    The reaction medium is vacuum-filtered in order to remove the sodium chloride formed over time and the catalyst. The salts are washed with epichlorohydrin which is then removed by evaporation under reduced rotavapor pressure. A purification step by distillation under reduced pressure (<1mBar) is carried out. The distillate obtained then corresponds to the diglycidyl ether of isosorbide in the form of a clear and colorless liquid (Brookfield viscosity at 20 ° C. of 218 mPa.s) having an epoxy equivalent of 132 g / equivalent, and having a mass content of 0.1% chlorine measured according to ISO 21627-3.
    Characteristics of the different compounds tested:
    The main characteristics of the epoxy resin and of the different reactive diluents tested in Table 1 are found (EE designates the equivalent of epoxy by weight which is measured according to the standard ISO 3001 or ASTM D1652).
    Table 1
    Example 1
    This example relates to the manufacture of compositions between the bisphenol A epoxy resin Diglycidylether (DGEBA) and various reagent diluents in various proportions, and the determination of the Brookfield viscosity at 20 ° C. of said compositions.
    To do this, 100 g of DGEBA epoxy resin is mixed at room temperature with 11.1 g of reactive diluent. The mixture is heated to 20 ° C. and the viscosity is measured using a Brookfield rotary viscometer, type DV-II +. The measurement is carried out after stabilization of the medium maintained at 20 ° C. using a thermostatically controlled water bath. The viscosity measurements are obtained with a torque (Torque) in% of the maximum torque between 10 and 100%.
    Throughout this application, the rate at which Brookfield viscosity is determined is not indicated. The person skilled in the art knows how to adapt it with respect to the choice of the rotor and so as to place himself at a percentage of the torque (Torque) of between 10 and 100%. Each composition is carried out in the same manner by increasing the amount of diluent so as to obtain compositions which comprise between 0 and 40% by weight of reactive diluent. For commercial diluents,% is understood as% in the state.
    Each composition is perfectly homogeneous and the viscosities at 20 ° C are collated in Table 2.
    Table 2
    Table 2 demonstrates that the introduction of 10% by weight of the reactive diluent according to the invention makes it possible to divide the viscosity of the mixture by two. In addition, viscosity levels comparable to those obtained with the products of the prior art are reached.
    Example 2
    This example relates to the crosslinking of the compositions obtained above, and to the determination of the glass transition temperatures of the compositions thus crosslinked.
    The crosslinking of the curable compositions of epoxy resins is carried out in the presence of an amine hardener: isophorone diamine. The quantity of isophorone diamine introduced is calculated in such a way that the ratio of the number of -NH groups to the number of epoxy groups is equal to 1. Isophorone diamine is available under the trademark Vestamid® IPD by Evonik. The equivalent of -NH group by weight is 42.5 g / eq. The formula used to calculate the diamine quantities to be used is as follows:
    By way of example, here is how the crosslinking of the mixture between the resin and 10% by weight of the reactive diluent according to the invention was carried out, the other tests having been carried out according to the same protocol while adapting the quantities of products. 90 g of epoxy resin are mixed at room temperature with 10 g of reactive diluent 1. Then, x = 23.7 g of isophorone diamine, (x being calculated using the above equation and depends on ΙΈΕ of the reactive diluent chosen ) are added and the mixture is stirred for 1 minute. The mixture, homogeneous and flowing at room temperature, is placed in a silicone mold (L = 43mm, l = 20mm). The crosslinking is carried out 1 day at ambient temperature followed by 1 day at 90 ° C. and 3 days at 130 ° C. in an oven. A material solid at room temperature and having a glass transition temperature (Tg) of 149 ° C. is then obtained. The glass transition temperature is measured by differential scanning calorimetry (DSC) at the second pass of a temperature ramp of -100 to 200 ° C. at 10 ° C./min. The values of Tg are reported in Table 3.
    Table 3
    Surprisingly, the glass transition temperatures are much higher with the use of the reactive diluent according to the invention. These results are particularly advantageous for the application of crosslinked compositions or crosslinked resins for the manufacture of objects, composites, coatings, adhesives, paints, inks, etc. may be exposed to high temperatures above 120 ° C without loss of properties during use.
    FIG. 1 represents, for each reactive diluent, the evolution of the glass transition temperature (Tg in ° C.) of the crosslinked resin or crosslinked composition measured in Example 2, as a function of the Brookfield viscosity of the composition before crosslinking ( in mPa.s, measured at 20 rpm and 20 ° C) measured in Example 1.
    Figure 1
    Figure 1 illustrates very clearly that the reactive diluent 1 according to the invention offers the best compromise between the viscosity of the mixture and the glass transition temperature of the crosslinked mixture.
    Example 3
    This example relates to the determination of a certain number of mechanical properties on the specimens obtained with the implementation of: no reactive diluent (test No. 1 according to the prior art) of 40% by weight of the reactive diluent 1 ( test No. 2 according to the invention) - 40% by weight of the reactive diluent 2 (test No. 3 according to the prior art).
    The mechanical properties are determined by tensile test on flat specimens: - Young's modulus or elasticity (MPa): corresponds to the mechanical stress which would give rise to an elongation of 100% of the initial length of the specimen (determined according to the method described in ASTM D638) - tensile strength (MPa): corresponds to the tensile stress exerted on a specimen until it breaks (determined by the method described in ASTM D638) - elongation at rupture: defines the ability of a material to elongate before failure (determined by the method described in ASTM D638) - toughness (K | C): characterizes the property of a material to resist fracture when is cracked. The higher the K | C value, the more material can absorb energy before breaking (determined by the method described in ASTM D5045).
    The results appear in Table 4. The numbers of the tests refer to the compositions indicated at the beginning of Example 3.
    Table 4 The incorporation of diglyciyl ether of isosorbide makes it possible to improve the mechanical properties and shock resistance dramatically.
    The reactive diluent according to the invention therefore has many advantages: it offers the best compromise between the viscosity of the mixture and the glass transition temperature of the crosslinked mixture; it leads to excellent mechanical properties; it significantly increases the toughness of the epoxy network, at least as much as 20% of a liquid elastomer of CTBN type, while keeping a very low initial viscosity and without having to deal with the problem of phase separation induced by the polymerization ( the network is homogenous from a thermodynamic point of view) which is the lot of all liquid elastomer type additives.
    权利要求:
    Claims (12)
    [1" id="c-fr-0001]
    1 - Use, as reactive diluent for the preparation of a polymerizable and / or crosslinkable composition of resin, adhesive, coating, or composite matrix, of at least one bis-anhydrohexitol ether of formula (I ):

    (I) - and having a Brookfield viscosity, measured at 20 ° C below 500 mPa.s.
    [2" id="c-fr-0002]
    2 - Use according to claim 1, characterized in that the compound of formula (I) has a Brookfield viscosity measured at 20 ° C preferably less than 400 mPa.s, very preferably less than 300 mPa.s and even more preferably between 50 and 300 mPa.s, and most preferably between 100 and 300 mPa.s.
    [3" id="c-fr-0003]
    3 - Use according to one of claims 1 or 2, characterized in that the compound of formula (I) has an equivalent epoxy by weight of between 129 and 145 g / eq, preferably between 129 and 136 g / eq.
    [4" id="c-fr-0004]
    4 - Use according to one of claims 1 to 3, characterized in that the compound of formula (I) has a mass content of chlorine less than 0.5%, preferably less than 0.3%.
    [5" id="c-fr-0005]
    5 - Use according to one of claims 1 to 4, characterized in that said polymerizable composition and / or crosslinkable is based on a polymerizable organic matrix epoxy type.
    [6" id="c-fr-0006]
    6 - polymerizable and / or crosslinkable composition of resin, adhesive, coating or matrix for composite, said composition comprising: a polymerizable and / or crosslinkable organic matrix; at least one bis-anhydrohexitol ether of formula (I):

    (I) - and having a Brookfield viscosity, measured at 20 ° C below 500 mPa.s.
    [7" id="c-fr-0007]
    7 - polymerizable composition and / or crosslinkable according to claim 6, characterized in that the compound of formula (I) has a Brookfield viscosity measured at 20 ° C preferably less than 400 mPa.s, very preferably less than 300 mPa.s and more preferably between 50 and 300 mPa.s, and most preferably between 100 and 300 mPa.s.
    [8" id="c-fr-0008]
    8 - polymerizable composition and / or crosslinkable according to one of claims 6 or 7, characterized in that the compound of formula (I) has an equivalent epoxy by weight of between 129 and 145 g / eq, preferably between 129 and 136 g / eq.
    [9" id="c-fr-0009]
    9 - polymerizable composition and / or crosslinkable according to one of claims 6 to 8, characterized in that the compound of formula (I) has a mass content of chlorine less than 0.5%, preferably less than 0.3%.
    [10" id="c-fr-0010]
    10 - polymerizable composition and / or crosslinkable according to one of claims 6 to 9, characterized in that the polymerizable organic matrix and / or crosslinkable is an epoxy resin.
    [11" id="c-fr-0011]
    11 - polymerizable composition and / or crosslinkable according to one of claims 6 to 10, characterized in that it further contains at least one accelerator and / or hardener.
    [12" id="c-fr-0012]
    12 - crosslinked composition obtained from the composition according to one of claims 6 to 11.
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    CN107922780A|2018-04-17|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    GB1002440A|1961-05-31|1965-08-25|Beck & Co Gmbh Dr|Hardenable compositions consisting of or including a hardenable synthetic resin and a heterocyclic epoxy ether as diluent|
    FR1445942A|1964-09-01|1966-07-15|Dynamit Nobel Ag|Process for the stabilization of diglycidyl ethers of 2, 2-bis- -propane|
    JPH01307935A|1988-06-07|1989-12-12|Seiko Epson Corp|Optical disk|
    WO2008147473A1|2007-05-31|2008-12-04|New Jersey Institute Of Technology|Thermoset epoxy polymers from renewable resources|
    FR3016631A1|2014-01-21|2015-07-24|Roquette Freres|PROCESS FOR PRODUCING GLYCIDYL ETHERS OF ISOHEXIDES PRODUCED THUS OBTAINED AND THEIR USES|WO2021089953A1|2019-11-08|2021-05-14|Roquette Freres|Epoxy resin comprising an isosorbide epoxide|US3041300A|1959-10-06|1962-06-26|Martin Marietta Corp|Polyglycidyl ethers of ether anhydro hexitols, method of production, and aqueous solutions thereof|
    US3272845A|1963-03-21|1966-09-13|Atlas Chem Ind|Bisglycidyl ethers of isohexides|
    US4770871A|1987-11-06|1988-09-13|Ici Americas Inc.|Process for the preparation of dianhydrosorbitol ethers|
    JP4535214B2|1999-10-08|2010-09-01|新日鐵化学株式会社|Flame retardant liquid epoxy resin composition|
    US20080021209A1|2006-06-01|2008-01-24|New Jersey Institute Of Technology|Ethers of bisanhydrohexitols|
    WO2012041816A1|2010-09-30|2012-04-05|Solvay Sa|Derivative of epichlorohydrin of natural origin|
    KR101272840B1|2011-05-19|2013-06-10|한국생산기술연구원|A photocurable 1,4:3,6-dianhydro-D-hexane-1,2,3,4,5,6-hexol derivative, a preparation method thereof and a photocurable composition comprising the same|
    JP2013054531A|2011-09-02|2013-03-21|Nomura Research Institute Ltd|Incident management system|
    EP2791199B1|2011-12-16|2015-09-16|3M Innovative Properties Company|Oxirane-containing bisanhydrohexitol derivatives and uses thereof|
    DE102012202161A1|2012-02-14|2013-08-14|Elantas Gmbh|Electrical insulating resin based on Isohexiddioldiglycidethern|
    EP2644589A1|2012-03-30|2013-10-02|Cytec Surface Specialties, S.A.|Radiation Curable acrylated Compounds|
    EP2858998A4|2012-06-11|2016-01-13|Archer Daniels Midland Co|Monoallyl, monoglycidyl ethers and bisglycidyl ethers of isohexides|
    US9605108B2|2014-04-24|2017-03-28|New Jersey Institute Of Technology|Isosorbide-derived epoxy resins and methods of making same|
    KR101660237B1|2014-07-18|2016-09-27|국도화학 주식회사|Preparation methode of Biobased Epoxy Resin and It's Composition for Cured System|WO2019122257A1|2017-12-21|2019-06-27|Elantas Europe S.R.L.|New use of isosorbide|
    FR3102986A1|2019-11-08|2021-05-14|Roquette Freres|An epoxy resin composition comprising an isosorbide epoxy and its use to stabilize a fibrous or porous material|
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    优先权:
    申请号 | 申请日 | 专利标题
    FR1557712|2015-08-13|
    FR1557712A|FR3040059B1|2015-08-13|2015-08-13|USE OF A LOW VISCOSITY BIS-ANHYDROHEXITOL ETHERS COMPOSITION AS A REACTIVE DILUENT FOR CROSS-LINKABLE COMPOSITIONS OF RESINS, ADHESIVES, COATINGS AND COMPOSITE MATRIXES|FR1557712A| FR3040059B1|2015-08-13|2015-08-13|USE OF A LOW VISCOSITY BIS-ANHYDROHEXITOL ETHERS COMPOSITION AS A REACTIVE DILUENT FOR CROSS-LINKABLE COMPOSITIONS OF RESINS, ADHESIVES, COATINGS AND COMPOSITE MATRIXES|
    CA2995162A| CA2995162A1|2015-08-13|2016-08-08|Use of a composition of low-viscosity bis-anhydrohexitol ethers as a reactive diluent for crosslinkable resin, adhesive, coating and matrix compositions for composites|
    JP2018506824A| JP2018522997A|2015-08-13|2016-08-08|Use of low viscosity bis-anhydrohexitol compositions as reactive diluents for crosslinkable resins, adhesives, coatings and matrix compositions for composites|
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    PCT/FR2016/052052| WO2017025687A1|2015-08-13|2016-08-08|Use of a composition of low-viscosity bis-anhydrohexitol ethers as a reactive diluent for crosslinkable resin, adhesive, coating and matrix compositions for composites|
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    US15/752,203| US10913817B2|2015-08-13|2016-08-08|Use of a composition of low-viscosity bis-anhydrohexitol ethers as a reactive diluent for crosslinkable resin, adhesive, coating and matrix compositions for composites|
    CN201680047707.5A| CN107922780B|2015-08-13|2016-08-08|Use of low viscosity dianhydrohexitol ether compositions as reactive diluents for crosslinkable resins, adhesives, coatings and composite matrix compositions|
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