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    • 专利摘要:
    The invention relates to a sizing composition for reinforcing fibers, which makes it possible to improve the adhesion of these fibers with respect to an organic matrix forming with them a part made of a composite material and resulting from the chain transfer polymerization of a curable resin, as well as to the applications of this composition. The sizing composition comprises a polybutadiene prepolymer comprising at least two epoxide functional groups, a crosslinking agent comprising at least two reactive functional groups of which at least one is a thiol function, and a catalyst comprising at least one tertiary amine function. Areas of use: aeronautics, aerospace, rail, naval and automotive industries, for example for the production of structural parts, engine, cabin or bodywork; the armaments industry, for example for the production of missile or missile-launcher parts; sports and leisure articles industry, for example for making articles for water sports and gliding.
    公开号:FR3017394A1
    申请号:FR1451099
    申请日:2014-02-12
    公开日:2015-08-14
    发明作者:Arnaud Martin；Brigitte Defoort；Xavier Coqueret
    申请人:Centre National de la Recherche Scientifique CNRS；Astrium SAS；Universite de Reims Champagne Ardenne URCA；
    IPC主号:
    专利说明:

    [0001] The present invention relates to the field of the sizing of reinforcing fibers (or reinforcing fibers) suitable for use in the manufacture of composite materials with organic matrix and fiberglass. BACKGROUND OF THE INVENTION reinforcement. More specifically, it relates to a sizing composition for reinforcing fibers, which improves the adhesion of these fibers vis-à-vis an organic matrix forming with them a piece of a composite material and resulting from the chain transfer polymerization of a curable resin. It also relates to the applications of this composition and, in particular, to a process for improving the adhesion of reinforcing fibers to an organic matrix forming with these fibers a part made of a composite material and resulting from the polymerization. by chain transfer of a curable resin, and which comprises a sizing of the reinforcing fibers by means of said composition. The invention makes it possible to obtain composite material parts with remarkable properties of resistance to stress, both transverse (that is to say in the direction perpendicular to the reinforcing fibers) and longitudinal (that is to say, in the direction perpendicular to the reinforcing fibers). say in the direction of the reinforcing fibers), finds a particular interest in the aeronautics, aerospace, rail, naval and automotive industries, whether for the production of structural parts, engine, cockpit or bodywork. However, it can also be used in other types of industry such as the arms industry, for example for the production of missile or missile launcher parts, or sports articles. and recreation, for example for making articles for water sports and boardsports. STATE OF THE PRIOR ART Composite materials are heterogeneous materials that make it possible to exploit the exceptional mechanical properties of materials that are not known to manufacture in massive form but only in the form of fibers by embedding them in a matrix formed of a hardened organic polymer (or resin), which makes it possible to bind the fibers together, to ensure stress distribution in the composite materials and to protect the fibers against chemical attack. A prerequisite for obtaining a high performance composite material is that the bond between the reinforcing fibers and the matrix constituting it is good. In fact, if the reinforcing fiber / matrix bond is insufficient, then a composite material with poor transverse mechanical properties (such as shear strength) is obtained and, therefore, with very limited possibilities of use, the composite material parts being often intended to work in a state of three-way stress.
    [0002] The fibers which are conventionally used as reinforcement material, such as carbon fibers naturally have a low adhesion to polymeric matrices. Also, manufacturers of reinforcing fibers have sought to adapt their fibers to resins intended to be used as dies by manufacturers of composite parts. This adaptation has been carried out in two different ways: * on the one hand, by surface treatments which all aim to create on the surface of the fibers functional groups capable of reacting with chemical functions carried by the resins; it is mainly chemical or electrolytic oxidation treatments (see, for example, JP-A-3-076869 [1]) but other types of treatment have also been proposed as heat treatments by plasma (see, for example, EP-A-1 484 435 [2]), an electrolysis in an acidic or basic medium (see EP-A-0 640 702 [3]) or the implantation of Si or B type atoms (see JP-B-2002-327374 [4]); and * on the other hand, by the use of specific sizes, that is to say by the deposition on the surface of the fibers of products whose role is to increase the compatibility of the fibers vis-à-vis the resins, to facilitate their impregnation with the resins and to ensure a "hooking" between the fibers and the matrices formed by the polymerization of these resins; in general, the sizing agents used are polymers or copolymers with complex chemical structures and whose choice is mainly guided by experience. It should be noted that sizes are also applied to the reinforcing fibers for purposes other than improving their bond with an organic matrix such as, for example, that of facilitating their handling, lubricating and protecting them from the abrasion that they can undergo while being rubbed against each other. If the treatments mentioned above are, in general, relatively effective in the case of matrices obtained by thermal (i.e. heat-induced) polymerization of resins, it turns out that they do not are not, or insufficiently, when the matrices are made with resins whose polymerization is induced by light radiation (visible or ultraviolet light) or by ionizing radiation (electron beam or X-rays). Indeed, experience shows that the composite materials obtained with polymerized resins whose polymerization is induced by light or ionizing radiation have transverse mechanical performance significantly lower than those of the best composite materials made with thermally polymerized resins, which which is conventionally interpreted as the fact that the bond reinforcing fibers / matrix remains insufficient despite the treatments applied to the reinforcing fibers by their manufacturers. However, the polymerization of resins under light or ionizing radiation has a certain number of advantages over the polymerization of resins thermally, these advantages being notably related to the possibility of working without autoclaves and, therefore, of making more easily composite parts of large size or complex structure, and to obtain much higher polymerization speeds, which allows higher production rates for lower costs. Recently, it has been proposed by the Applicant, to improve the adhesion between carbon fibers and a matrix obtained by polymerization of a polymerizable resin by chain transfer (since in practice the resins which are capable of polymerizing under light or ionizing radiation are resins whose polymerization is carried out by a chain transfer mechanism) by grafting onto the surface of the fibers groups capable of serving as chain transfer agents during the polymerization of the resin (see EP-A-1,924,727 [5]) or by depositing on the surface of the fibers a polymer film comprising groups capable of serving as chain transfer agents during the polymerization of the resin (see EP-A-2,099). 849 [6]). Continuing its work on the improvement of the transverse mechanical properties of composite materials, the Depositor set itself the aim of providing a new solution to the problem of the lack of adhesion existing between reinforcing fibers and, in particular, carbon fibers. and the organic matrix in which these fibers are embedded when this matrix is obtained by polymerization of a polymerizable resin under light or ionizing radiation, that is to say in practice by a chain transfer mechanism. SUMMARY OF THE INVENTION This and other objects are achieved by the invention which proposes, firstly, a sizing composition, which comprises: a polybutadiene prepolymer comprising at least two epoxide functional groups, more simply called "epoxidized polybutadiene prepolymer" " in the following ; a crosslinking agent comprising at least two reactive functions of which at least one is a thiol function; and a catalyst comprising at least one tertiary amine function. Thus, according to the invention, is associated in the same sizing composition: * an epoxidized polybutadiene prepolymer able to form, by polymerization and crosslinking, a homogeneous elastomeric film on a surface of the reinforcing fibers; a crosslinking agent which has a dual role: on the one hand, that of permitting the crosslinking of the epoxidized polybutadiene prepolymer on the surface of the fibers, by reaction with the epoxide functions that this prepolymer comprises, and, on the other hand, that of establishing thiol functions - via the epoxidized polybutadiene film - on the surface of the reinforcing fibers; and a tertiary amine catalyst whose role is to catalyze the reaction between the epoxide functions of the epoxidized butadiene prepolymer and the reactive functions of the crosslinking agent to allow the formation of a network from this prepolymer. The elastomeric film which forms on the surface of the fibers, after polymerization and crosslinking of the epoxidized polybutadiene prepolymer, makes it possible, when the reinforcing fibers are subsequently brought into contact with a resin which can be hardened by chain transfer polymerization: to give the fibers a homogeneous surface state, the surface of the elastomeric film actually replacing the surface of these fibers; isolating the surface of the fibers of the curable resin and thus preventing the polymerization of this resin from being inhibited by the reactive functions present on the surface of the fibers as a result of their manufacturing process; and - covering the fibers with thiol functions which will (1) sensitize the polymerization of the curable resin and (2) act as chain transfer agents during the polymerization of this resin and thus prime, by transformation into active centers the formation, from the surface of the elastomeric film, of new polymer resin chains which will be covalently bound to this surface as soon as they are created, thus improving the quality of the bonding between the fibers and the organic matrix resulting from the polymerization curable resin. In addition, the reactive functions that comprise the epoxidized polybutadiene prepolymer and the crosslinking agent are capable of reacting with the reactive functions present on the surface of the fibers as a result of their manufacturing process and thus form covalent bonds between the fibers and the polymer. elastomeric film which, too, will contribute to improving the quality of the interface between the fibers and the organic matrix resulting from the polymerization of the curable resin.
    [0003] This results in a very significant increase in the adhesion between the reinforcing fibers and the organic matrix resulting from the polymerization of the curable resin and therefore the transverse mechanical properties of the composite materials formed by these fibers and this matrix. According to the invention, the epoxidized polybutadiene prepolymer preferably comprises at least two repeating units chosen from the following units of formulas (I) and (II): (III) Epoxidized polybutadiene prepolymers of this type are, for example, for example, the prepolymers which are marketed by the companies Sartomer and Cray Valley under the trade references Poly bdTM 600E and Poly bdTM 605E. These prepolymers schematically correspond to the following formula (IV): (I) (II) and at least two repeating units of formula (III) below: wherein n is the number of repeating units present between hooks, and typically have the following physico-chemical characteristics: molecular weight (Me) of about 1300; - epoxy equivalent weight (EEW) of 400-500 g / mole for Poly bdTM 600E and 260-330 g / mole for Poly bdTM 605E; and - viscosity at 30 ° C of 7 Pa.s for Poly bdTM 600E and 22 Pa.s for Poly bdTM 605E. As previously indicated, the crosslinking agent comprises at least two reactive functions of which at least one is a thiol function. According to the invention, this crosslinking agent may in particular be chosen from compounds which comprise: a carboxylic acid function and a thiol function such as, for example, thioglycolic acid, thiolactic acid, 3-mercaptopropionic acid; 11-mercaptoundecanoic acid or 16-mercaptohexadecanoic acid; a non-aromatic amine function (i.e., not linked to one or more aromatic rings) and a thiol function such as, for example, cysteamine; two carboxylic acid functional groups and a thiol group such as, for example, thiomalic acid, mercaptosuccinic acid and dimercaptosuccinic acid; a carboxylic acid function, a non-aromatic amine function and a thiol function such as, for example, cysteine; two thiol functions such as, for example, 1,2-ethanedithiol, 1,3-propanedithiol, 1,4-butanedithiol, 2,3-butanedithiol or 1,5-pentanedithiol; or else three thiol functions such as, for example, pentaerythritol tetrakis (3 mercaptopropionate), pentaerythritol tetrakis (2-mercaptoacetate), trimethylolpropane tris (3-mercaptopropionate) or tris [2- (3merca ptopropionyloxy) ethyl). ] isocya n urate.
    [0004] Preferably, the crosslinking agent is a trifunctional compound, that is to say to three reactive functions, in which case it is advantageously chosen from compounds which comprise two carboxylic acid functions and a thiol function, for example mercaptosuccinic acid, and compounds which comprise three thiol functions, such as, for example, pentaerythritol tetrakis (3-mercaptopropionate). The catalyst is advantageously chosen from 2- (dimethylamino) ethyl methacrylate, 2- (dimethylamino) ethyl acrylate, 2- (diethylamino) ethyl acrylate and 3- (dimethylamino) acrylate. propyl.
    [0005] According to the invention, the composition preferably comprises, in percentages by weight, based on its total mass: from 45 to 96% and more preferably from 55 to 72% of epoxidized polybutadiene prepolymer; from 2.5 to 55% and more preferably from 27 to 45% of crosslinking agent; and from 0.1 to 2.2% of catalyst. For its application on reinforcing fibers, the sizing composition according to the invention may be in the form of a solution. In this case, it further comprises an organic solvent such as methyl ethyl ketone, tetrahydrofuran, ethyl methyl ether, ethyl acetate or a mixture thereof. In this case also, the epoxidized polybutadiene prepolymer, the crosslinking agent and the catalyst together represent, in percentages by weight relative to the total mass of the composition, from 0.5 to 5% and more preferably from 1 to 3% while the organic solvent is, in percentages by weight, based on the total mass of the composition, from 95 to 99.5% and, more preferably, from 97 to 99%. Alternatively, the sizing composition can also be in the form of an organic (or dispersed) organic phase and aqueous phase (or dispersant) phase emulsion so as to limit the use of organic solvents and thus preserve at best, the safety of those who may prepare or use this sizing composition and the environment. In this case: either the crosslinking agent is a compound soluble in organic solvents, as are, for example, thiol-functional compounds such as pentaerythritol tetrakis (3-mercaptopropionate), then the internal phase; organic composition preferably comprises an organic solvent, immiscible with water, in which the epoxidized polybutadiene prepolymer, the crosslinking agent and the catalyst are located, whereas the aqueous external phase preferably comprises water. wherein there is a surfactant (or surfactant); or the crosslinking agent is an insoluble or poorly soluble compound in organic solvents - as is the case, for example, compounds with two carboxylic acid functions and a thiol function such as mercaptosuccinic acid -, then the phase organic internal composition preferably comprises an organic solvent, immiscible with water, in which the epoxidized polybutadiene prepolymer is located, while the aqueous external phase preferably comprises water in which the crosslinking, the catalyst and a surfactant. Preferably, the organic solvent present in the emulsion is ethyl acetate.
    [0006] Also preferably, the surfactant is a nonionic surfactant such as, for example, poly (ethylene glycol) or anionic diacrylate such as, for example, sodium dodecyl sulphate (or sodium lauryl sulphate) or lauryl sulphate. ammonium. More preferably, the weight of the organic inner phase is from 1 to 6% and more preferably from 1 to 3% of the weight of the aqueous outer phase. Such an emulsion can in particular be obtained by adding a solution which comprises, as the case may be, both the epoxidized polybutadiene prepolymer, the crosslinking agent and the catalyst, or only the epoxidized polybutadiene prepolymer, in the non-miscible organic solvent. water, to an aqueous solution which comprises, as appropriate, only the surfactant, or both the crosslinking agent, the catalyst and the surfactant, in water, and subjecting all to vigorous agitation, for example mechanical or ultrasound. The emulsion thus obtained is stable and has droplets, which are formed either by the epoxidized polybutadiene prepolymer, the crosslinking agent and the catalyst in the case where the crosslinking agent and the catalyst are present in the organic internal phase, either solely by the epoxidized polybutadiene prepolymer in the case where the crosslinking agent and the catalyst are present in the aqueous external phase, and most of which typically have a mean diameter (or equivalent diameter) ranging from 50 nm to 200 nm . Whatever the form in which the sizing composition is present (solution or emulsion), the sizing of reinforcing fibers with this composition is extremely simple to implement. Indeed, it suffices to soak the fibers, for example by means of an inking roll, in a bath consisting of the sizing composition according to the invention the time required to obtain the deposition of a layer on the surface of the fibers. typically representing 0.5 to 1.5% by weight of the mass of the fibers, then subjecting the fibers, after their removal from the sizing bath, to a heat treatment, for example at a temperature ranging from 60 to 180 ° C and for a period ranging from 0.3 to 3 hours depending on the type of epoxidized polybutadiene prepolymer used, to obtain the formation of a homogeneous elastomeric film on the fiber surface by polymerization / crosslinking of this prepolymer. The subject of the invention is also a process for sizing reinforcing fibers, which is characterized in that it comprises the application of at least one layer of a sizing composition as previously described on a surface of fibers and the heat treatment of the layer thus applied. In this process, the application of at least one layer of the sizing composition and the heat treatment which is applied to this layer may in particular be carried out as described above.
    [0007] The invention further relates to reinforcing fibers, which comprise a size and which are characterized in that the size is formed by applying at least one layer of a sizing composition as previously described on the surface of the fibers and heat treatment of the layer thus applied.
    [0008] The reinforcing fibers thus sized can either be immediately used in the manufacture of parts made of composite materials, or they may be stored for later use or they may be packaged, for example in the form of prepregs, for delivery to manufacturers of composite material parts. Indeed, the invention can be implemented by the manufacturers of reinforcing fibers as well as by their users. According to a preferred arrangement of the invention, the reinforcing fibers are carbon fibers. However, it may also be glass fibers, quartz fibers, graphite fibers, metal fibers, poly (p-phenylene benzobisoxazole) fibers, aramid fibers, polyethylene fibers, boron fibers, silicon carbide fibers, natural fibers (for example, flax, hemp or bamboo fibers) and mixtures of fibers of different types, for example carbon / glass, carbon / aramid, etc. Moreover, the reinforcing fibers may be in various forms such as cut son, crushed fibers, continuous filament mats, mats with cut filaments, rovings (also known as "rovings" in English), fabrics, knits, felts, etc., or in the form of complexes made by association of different types of planar materials. The invention also relates to a method for improving the adhesion of reinforcing fibers to an organic matrix forming with the fibers a part made of a composite material, the part being obtained by contacting the fibers with a resin which can be hardened by chain transfer polymerization, and then polymerization of the resin, which process comprises, before the fibers are brought into contact with the resin, a sizing of the fibers by application of at least one a layer of a sizing composition as previously described on a surface of the fibers and heat treatment of the layer thus applied. The subject of the invention is also a process for manufacturing a part made of a composite material comprising reinforcing fibers in an organic matrix, which method comprises bringing the reinforcing fibers into contact with a resin that can be hardened by chain transfer polymerization. and the polymerization of the resin, and is characterized in that it further comprises, before the fibers are brought into contact with the resin, a sizing of the fibers by application of at least one layer of a composition of sizing as described above on a surface of the fibers and heat treatment of the layer thus applied. In the processes above, the reinforcing fibers are, here again, preferably carbon fibers. As for the curable resin, it can be chosen from all the resins which are capable of hardening by a mechanism of polymerization by chain transfer and this, whether under the effect of heat or under the effect of radiation bright or ionizing. However, for the reasons previously set out, the curable resin is preferably chosen from resins polymerizable under light or ionizing radiation and, in particular, from polyesters, epoxides (such as diglycidyl ether epoxides of bisphenol A or DGEBA). ), epoxy (meth) acrylates (also known as vinyl esters or epoxyvinyl esters, such as di (meth) acrylates of DGEBA), (meth) acrylates with urethane nucleus, bis-maleimides, elastomers, silicones, epoxies ( meth) acrylates being particularly preferred in the case where the composite material part is intended for space or aeronautical applications. It goes without saying that the manufacture of the composite material part can be carried out according to all the techniques known to those skilled in the art of composite materials such as, for example, filament winding molding, simultaneous projection molding, molding under Vacuum Transfer Molding, Resin Transfer Molding (RTM), Low Pressure Wet Press Molding, Compression Molding (SMC) for Sheet Molding Compound In addition to the advantages mentioned above, the invention also offers the advantages of being applicable to a large number of types of reinforcing fibers used in the manufacture of composite materials (long, semi-long fibers, short fibers). , oxidized fibers, fibers already sized by their suppliers, etc.), to use only products available commercially and to be able to at costs compatible with an industrial scale operation. Other features and advantages of the invention will appear better on reading the additional description which follows and which refers to the appended figures. Of course, this additional description is given by way of illustration of the invention and does not constitute in any way a limitation thereof. BRIEF DESCRIPTION OF THE FIGURES FIGS. 1A and 1B illustrate the effects of various additives on the polymer conversion of an acrylate monomer by radical polymerization, initiated by ionizing radiation, as appreciated by steric exclusion chromatography; FIG. 1A shows the sensitizing effect of a thiol-functional additive, dodecanethiol-1 (-), while FIG. 1B shows the inhibitory effect of two hydroxyl-functional additives, phenol ( ---) and 9-phenanthrol (-A-), and an amine-functional additive, 1-aminopyrene (- ^ -); in each of these figures, the dashed line corresponds to the polymerization of the acrylate monomer in the absence of additive. FIGS. 2A, 2B and 2C illustrate the beneficial effects of the use of a sizing composition according to the invention on the adhesion between a substrate and an organic matrix obtained by radical polymerization of an epoxidized bisphenol A diacrylate monomer ; FIGS. 2A and 2B correspond to the adhesion test results obtained for two substrates consisting of carbon sheets, treated with sizing compositions according to the invention, while FIG. 2C corresponds to the result of a adhesion test having been obtained for a substrate also consisting of a carbon sheet, but untreated. FIG. 3 illustrates the number distribution of the mean diameter, expressed in nm, of the droplets of a sizing composition according to the invention in the form of an aqueous external phase emulsion, as determined from three measurements made by dynamic light scattering. DETAILED DESCRIPTION OF PARTICULAR EMBODIMENTS EXAMPLE 1 Demonstration of the Sensitizing Effect of a Thiol-Based Additive on the Radical Polymerization of an Acrylate Monomer Under Ionizing Radiation The sensitizing effect of a thiol-functional additive on the radical polymerization of an acrylate monomer, initiated by ionizing radiation, is evidenced by tests which consist in: mixing n-butyl acrylate (ABu) with dodecanethiol-1 at a rate of 0.5, 1 , 2, 5 and 10% by weight, based on the total mass of the mixtures; subjecting the resulting mixtures to ionizing radiation (electron beam ionisation) at a dose of 50 kGy in a single pass; and determining, for each mixture thus subjected to this ionizing radiation, the degree of conversion of n-butyl acrylate to poly (n-butyl acrylate) by size exclusion chromatography (CES).
    [0009] The CES is performed using a PL-GPC 50 Plus system, combined with a PL-ASRT automatic injector (Polymer Laboratories, Varian Incorporated). The detector used is a differential refractometer (RI). The CES system consists of three columns (PLgel 5 i.tm Mixed-C, 300 x 7.5 mm) in series. It also includes a pre-column (PLgel 5 i.tm Guard, 50 x 7.5 mm), which brings the total column length to 950 mm for an analysis time of 38 minutes. Tetrahydrofuran is used as a solvent with a flow rate of 1 mL / min, the injection volume is 100 μL and the oven temperature is 35 ° C. Samples are made in 4 mL pillboxes and diluted to a concentration of about 1 mg / mL. The solutions thus obtained are filtered on MilliporeTM filters (pore diameter: 0.20 μm).
    [0010] The degree of conversion, denoted TC, of n-butyl acrylate to poly (n-butyl acrylate) is determined by means of a calibration of the chromatography with solutions containing poly (n-butyl acrylate) masses and known n-butyl acrylate masses.
    [0011] For a sample, it corresponds to the ratio of the mass of poly (n-butyl acrylate), denoted mpAB 2, present in this sample to the total mass of poly (n-butyl acrylate) and n-acrylate. butyl, denoted mABU, present in this same sample: The results of these tests are illustrated in FIG. 1A, which represents the evolution of the conversion rate Tc as a function of the mass content of dodecanethiol-1 (-) as well as that obtained in the absence of additive (dotted line). This figure shows that a sensitizing effect of dodecanethiol-1 on the radical polymerization of n-butyl acrylate is observed as soon as a very small amount of this thiol is added (0.5% by mass) and that the conversion monomer to polymer is doubled, compared to what it is in the absence of additive, for a mass content of 10% dodecanethiol-1. By way of comparison, FIG. 1B illustrates the results obtained in tests having been carried out like the preceding ones but using as additives phenol (---), 9-phenanthrol (-A-) and 1-aminopyrene. (- ^ -) at 1, 2 and 5% by mass and by subjecting the n-butyl acrylate / additive mixtures to an ionizing radiation dose of 10 kGy. Here again, this figure represents the evolution of the conversion rate of n-butyl acrylate to poly (n-butyl acrylate) as a function of the mass content of phenol (-), 9-phenanthrol (- A-) and 1-aminopyrene (- ^ -) as well as that obtained in the absence of additive (dashed line). This figure shows that hydroxyl-functional additives such as phenol and 9-phenanthrol, or with an aromatic amine function, such as 1-aminopyrene, have, unlike a thiol-functional additive such as dodecanethiol-1, a strongly inhibiting effect. on the conversion of n-butyl acrylate to poly (n-butyl acrylate) and this at mass contents as low as 1%, this inhibitory effect being particularly pronounced for 9-phenanthrol and 1-aminopyrene. EXAMPLE 2 Demonstration of the beneficial effects of the use of a sizing composition according to the invention on the adhesion between a substrate and an organic matrix 2.1. At the macroscopic scale: Two sheets of carbon are treated ( Goodfellow company, reference C 000440/13), hereinafter referred to as sheets 1 and 2, by a sizing composition according to the invention which comprises: in the case of sheet 1: the Poly bdTM 605E prepolymer from Sartomer as the epoxidized polybutadiene prepolymer, mercaptosuccinic acid as crosslinking agent, 2- (dimethylamino) ethyl methacrylate as a catalyst, in the following proportions: 71.7% of epoxidized polybutadiene prepolymer, 26 9% of crosslinking agent and 1.4% of catalyst, the whole being in solution at a level of 1 to 2% by weight in tetrahydrofuran; and in the case of sheet 2: the same constituents as those indicated above with the exception of the crosslinking agent, which is pentaerythritol tetrakis (3-mercaptopropionate), in the following proportions by weight: 61.7 % of epoxidized polybutadiene prepolymer, 37.7% of crosslinking agent and 0.6% of catalyst, the whole being in solution at a level of 1 to 2% by weight in tetrahydrofuran. The sheets 1 and 2 are immersed in the sizing composition, then removed from this composition and subjected to a heat treatment (100 ° C. for 1 hour) to induce the polymerization / crosslinking of the epoxidized polybutadiene prepolymer and, thus, the formation of an elastomeric film on their surface. Then, an epoxidized bisphenol A diacrylate monomer resin (UCB Chemicals, reference EB600) is deposited on the upper part of the sheets 1 and 2 as well as on the upper part of a third carbon sheet, which is intended to serve as a reference sheet and which has not been treated with a sizing composition according to the invention. In all cases, the resin is spread, using a spiral filmograph, in a layer 20 microns thick, so as to cover the entire surface of the sheets. The resin is radically polymerized under electron beams by means of a low energy electron accelerator (145 keV) of the Application Development Unit type (Advanced Electron Beams Company). The total dose applied is 150 kGy. Each of the sheets 1, 2 and reference is subjected to adhesion tests that are carried out according to ISO 2409. These tests, which make it possible to evaluate the level of adhesion of a coating on a substrate, are based on a method called "grid" which involves incising the coating with a comb comprising 11 teeth spaced from each other by 1 mm (Braive-Instrument company, reference 1540) so as to obtain a grid surface. The grid is obtained by applying a uniform pressure on the comb and making two incisions at 90 °. The detachable parts, which are not left with the incisional movements, are removed by means of an adhesive tape (TesaTM 4120) which is applied by pushing with a finger on the grid surface and then rapidly withdrawn at an angle approaching the no more than 180 °. The level of adhesion of the coating on the substrate is evaluated by comparison with images representative of the degree of degradation of the coating and referenced by ISO values.
    [0012] The results of the adhesion tests thus carried out are illustrated in FIGS. 2A, 2B and 2C, FIG. 2A corresponding to sheet 1, FIG. 2B corresponding to sheet 2 and FIG. 2C corresponding to the reference sheet. As shown in these figures, the sheets treated with a sizing composition according to the invention (FIGS. 2A and 2B) have a high adhesion towards the hardened resin (with a measured ISO classification of 0) and this, regardless of the thiol-functional cross-linking agent (s) used, in contrast to the reference sheet (FIG. 2C) for which delamination of the resin is observed and an ISO classification of 5 is obtained. 2.2 - On composite materials: Two families of composites, hereinafter referred to as families 1 and 2, are prepared by treating carbon fibers (Toho Tenax Europe, reference IMS 5001 24k) by sizing compositions according to the invention and then impregnating the thus treated carbon fibers with an epoxidized bisphenol A diacrylate monomer resin (UCB Chemicals, reference EB600) and subjecting this resin to electron beam radical polymerization. The carbon fibers used are ex-PAN fibers with an intermediate modulus, not sized but having undergone a surface electrolytic oxidation treatment during their manufacture. In the case of the composite family 1, the carbon fibers are treated with sizing compositions which comprise the Poly bdTM 605E prepolymer from Sartomer as an epoxidized polybutadiene prepolymer, mercaptosuccinic acid as an agent. crosslinking and 2- (dimethylamino) ethyl methacrylate as a catalyst, the whole being in solution at a level of 1 to 2% by weight in ethyl and methyl ether. Three types of sizing compositions, which differ only in the mass proportions of their constituents, are used, namely: composition Al: 79% of epoxidized polybutadiene prepolymer; 20% crosslinking agent and 1% catalyst; composition B1: 71.7% of epoxidized polybutadiene prepolymer; 26.9% crosslinking agent and 1.4% catalyst; composition C1: 65.5% of epoxidized polybutadiene prepolymer; 32.8% crosslinking agent and 1.7% catalyst.
    [0013] In the case of composite 2, the carbon fibers are treated with sizing compositions which comprise the same constituents as those indicated above with the exception of the crosslinking agent, which is tetrakis (3-mercaptopropionate). pentaerythritol. Here again, three types of sizing compositions, which differ only in the mass proportions of their constituents, are used, namely: composition A2: 70.7% of epoxidized polybutadiene prepolymer; 28.8% crosslinking agent and 0.5% catalyst; composition B2: 61.7% of epoxidized polybutadiene prepolymer; 37.7% crosslinking agent and 0.6% catalyst; composition C2: 54.7% of epoxidized polybutadiene prepolymer; 44.6% crosslinking agent and 0.7% catalyst. In all cases, the sizing compositions are applied to the carbon fibers by means of a chain-type device to be impregnated. The carbon fiber locks are thus unwound and brought to an impregnation stand by means of a pulley system. The stand contains an impregnation tray on which is placed an ink roller which bathes in one of the sizing compositions. After impregnation with this composition, the carbon fibers are rewound around a virgin roll. The mass content of sizing composition deposited on the surface of each carbon fiber is 0.8 ± 0.3%.
    [0014] Then, the carbon fibers are subjected to heat treatment (100 ° C for 1 hour) to induce the polymerization / crosslinking of the epoxidized polybutadiene prepolymer and, thus, the formation of an elastomeric film on their surface. They are then impregnated with the epoxidized bisphenol A diacrylate monomer resin using the same device to be impregnated as that previously used for applying the sizing compositions. The mass content of impregnation of the carbon fibers with the resin is 39 ± 3%. The composites are prepared from wound plies of the fibers thus impregnated and are assembled so that these fibers are all oriented in the same direction (unidirectional plate). The assembly of the folds takes place in a cycle comprising steps of draping, compacting and assembling the folds. The compaction is carried out using a vacuum bag so as to eliminate as much porosity as the draping. The compaction cycle is carried out following a heat treatment of 80 ° C for 2 hours. The plates thus obtained are left in the "vacuum bags" in order to carry out the polymerization of the resin under electron beams.
    [0015] This polymerization is carried out using a high energy electron accelerator (10 MeV) of the CirceTM II type. The total dose applied is 100 kGy per 2 passages at 50 kGy. In each family of composites, a part of the composites is subjected to a so-called post-cure treatment which consists of a heat treatment at 160 ° C. for 1 hour. Composite reference materials are prepared in parallel in the same manner as described above, but using carbon fibers that have not been previously treated with a sizing composition according to the invention.
    [0016] Each of the composites of families 1 and 2 and reference is subjected to tests in 3-point bending in the transverse direction according to the standard NF EN 2746, by means of an Instron 5566A test machine equipped with a force sensor 10 kN. The results of these tests are presented in Table I below. Table I Composites Sigma 2 in transverse flexion (MPa) Composites of reference 20 - 26 Composites of Without post-cooking 39 - 43 family 1 With post-cooking 49 - 60 Composites of Without post-cooking 46 - 54 family 2 With post This table shows that the composite materials comprising carbon fibers that have been treated with a sizing composition according to the invention have a significantly improved transverse bending strength compared with that of a composite material comprising untreated fibers, especially since these composite materials have been subjected to a post-baking treatment.
    [0017] EXAMPLE 3 Preparation of a sizing composition according to the invention in the form of an emulsion with an organic internal phase and an aqueous external phase A sizing composition according to the invention is obtained in the form of an emulsion with internal organic phase and aqueous external phase by proceeding as follows. A solution comprising 1 g of Poly bdTM 605E prepolymer from Sartomer in 10 ml of ethyl acetate is prepared. A 1 g solution of pentaerythritol tetrakis (3-mercaptopropionate) is prepared in parallel in 3 ml of ethyl acetate and 5 mol%, relative to the number of moles of tetrakis (pentaerythritol 3-mercaptopropionate, methacrylate of 2 The two true solutions thus obtained are mixed together and the resulting mixture is gradually added to 40 ml of a solution containing 2% by weight of sodium dodecyl sulphate in water.
    [0018] Then, the whole is emulsified by means of a rotor-stator type homogenizer which is used at a rotation speed of 24,000 rpm for two minutes. The emulsion thus obtained is subjected to a Dynamic Light Scattering (DLS) analysis to measure the size of the droplets present in this emulsion. The results of this analysis are illustrated in FIG. 3 which represents the number distribution of the average diameter (or equivalent diameter), expressed in nm, of the droplets of the emulsion as determined from three measurements by DLS. They show that the population of the largest size droplet has an average diameter of 122.4 nm. The average diameter of the population of the majority size droplets is therefore in the range of 50 to 150 nm expected. The smallest droplets have an average diameter of 68 nm and represent less than 1% of the droplets present in the emulsion. Likewise, at most 1% of the droplets has a mean diameter greater than 550 nm.
    [0019] The emulsion is therefore composed mainly of droplets for having a stable emulsion and it is composed entirely of droplets to obtain the formation of a homogeneous elastomeric film on the surface of a substrate.
    [0020] The stability of the emulsion is confirmed by an accelerated aging test which consists of subjecting it to centrifugation at a rotation speed of 1000 rpm for 5 minutes and at the end of which no demulsification is observed. REFERENCES CITED [1] Japanese Patent Application No. 3-076869 European Patent Application No. 1,484,435 European Patent Application No. 0,640,702 Japanese Patent No. 2002-327374 [2] European Patent Application No. 1,924 727 European Patent Application No. 2,099,849 [3] [4] [5] [6]
    权利要求:
    Claims (21)
    [0001]
    REVENDICATIONS1. Sizing composition, characterized in that it comprises: a polybutadiene prepolymer comprising at least two epoxide functional groups; a crosslinking agent comprising at least two reactive functions of which at least one is a thiol function; and a catalyst comprising at least one tertiary amine function.
    [0002]
    2. Composition according to claim 1, characterized in that the polybutadiene prepolymer comprises at least two repeating units chosen from the units of formulas (I) and (II) below:
    [0003]
    3. Composition according to claim 1 or claim 2, characterized in that the crosslinking agent is chosen from compounds which comprise a carboxylic acid function and a thiol function, a non-aromatic amine function and a thiol function, two functions. carboxylic acid and a thiol function, a carboxylic acid function, a non-aromatic amine function and a thiol function, two thiol functions or three thiol functions. (I) (II) and at least two repeating units of formula (III) below:
    [0004]
    4. Composition according to claim 3, characterized in that the crosslinking agent is chosen from compounds which comprise two carboxylic acid functions and a thiol function, or three thiol functions.
    [0005]
    5. Composition according to Claim 4, characterized in that the crosslinking agent is chosen from thiomalic acid, mercaptosuccinic acid, dimercaptosuccinic acid, pentaerythritol tetrakis (3-mercaptopropionate), tetrakis (2- pentaerythritol), trimethylolpropane tris (3-mercaptopropionate) and tris [2- (3-mercaptopropionyloxy) ethyl] isocyanurate.
    [0006]
    6. Composition according to any one of claims 1 to 5, characterized in that the catalyst is selected from 2- (dimethylamino) ethyl methacrylate, 2- (dimethylamino) ethyl acrylate, acrylate 2- (diethylamino) ethyl and 3- (dimethylamino) propyl acrylate.
    [0007]
    7. Composition according to any one of claims 1 to 6, characterized in that it comprises in percentages by weight relative to the total mass of the composition: from 45 to 96% of polybutadiene prepolymer; from 2.5 to 55% of crosslinking agent; and from 0.1 to 2.2% catalyst.
    [0008]
    8. Composition according to any one of claims 1 to 7, characterized in that it is in the form of a solution and further comprises an organic solvent
    [0009]
    9. Composition according to claim 8, characterized in that the organic solvent is selected from methyl ethyl ketone, tetrahydrofuran, ethyl methyl ether, ethyl acetate and mixtures thereof.
    [0010]
    10. Composition according to claim 8 or claim 9, characterized in that the polybutadiene prepolymer, the crosslinking agent and the catalyst together represent, in percentages by weight relative to the total mass of the composition, from 0.5 to 5%. while the organic solvent represents, in percentages by weight, based on the total mass of the composition, from 95 to 99.5%.
    [0011]
    11. Composition according to any one of claims 1 to 7, characterized in that it is in the form of an organic phase internal emulsion and aqueous external phase.
    [0012]
    12. Composition according to claim 11, characterized in that the organic internal phase comprises the polybutadiene prepolymer, the crosslinking agent and the catalyst in an organic solvent, immiscible with water, while the aqueous external phase comprises an agent surfactant in water.
    [0013]
    13. Composition according to claim 11, characterized in that the organic internal phase comprises the polybutadiene prepolymer in an organic solvent, immiscible with water, while the aqueous external phase comprises the crosslinking agent, the catalyst and an agent. surfactant in water.
    [0014]
    14. Composition according to any one of claims 11 to 13, characterized in that the internal organic phase mass represents 1 to 6% of the mass of the aqueous external phase.
    [0015]
    15. A method of sizing reinforcing fibers, characterized in that it comprises the application of at least one layer of a sizing composition according to any one of claims 1 to 14 on a surface of the fibers and the heat treatment of the layer thus applied.
    [0016]
    16. Reinforcing fibers comprising a sizing, characterized in that the size is formed by applying at least one layer of a sizing composition according to any one of claims 1 to 14 on the surface of the fibers and treatment thermal layer thus applied.
    [0017]
    17. Fibers according to claim 16, characterized in that they are carbon fibers.
    [0018]
    18. Process for improving the adhesion of reinforcing fibers to an organic matrix forming with the fibers a part made of a composite material, the part being obtained by bringing the fibers into contact with a resin which can be hardened by polymerization by chain transfer, then polymerization of the resin, characterized in that it comprises, before the fibers are brought into contact with the resin, a sizing of the fibers by applying at least one layer of a sizing composition according to any one of claims 1 to 14 on a surface of the fibers and heat treatment of the layer thus applied.
    [0019]
    A method of manufacturing a composite material part comprising reinforcing fibers in an organic matrix, comprising contacting the reinforcing fibers with a chain transfer polymerizable resin and the polymerization of the resin, characterized in that it further comprises, before the fibers are brought into contact with the resin, a sizing of the fibers by applying at least one layer of a sizing composition according to any one of claims 1 to 14 on a surface of the fibers and heat treatment of the layer thus applied.
    [0020]
    20. The method of claim 18 or claim 19, characterized in that the reinforcing fibers are carbon fibers.
    [0021]
    21. Process according to claim 18, wherein the curable resin is chosen from polyesters, , elastomers and silicones.5
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    同族专利:
    公开号 | 公开日
    ES2712749T3|2019-05-14|
    EP3105277B1|2018-09-26|
    WO2015121274A1|2015-08-20|
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    US20160355645A1|2016-12-08|
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    优先权:
    申请号 | 申请日 | 专利标题
    FR1451099A|FR3017394B1|2014-02-12|2014-02-12|ENSIMAGE COMPOSITION FOR REINFORCING FIBERS AND ITS APPLICATIONS|FR1451099A| FR3017394B1|2014-02-12|2014-02-12|ENSIMAGE COMPOSITION FOR REINFORCING FIBERS AND ITS APPLICATIONS|
    PCT/EP2015/052817| WO2015121274A1|2014-02-12|2015-02-11|Sizing composition for reinforcing fibres and applications thereof|
    ES15706709T| ES2712749T3|2014-02-12|2015-02-11|Sizing composition for reinforcing fibers and applications thereof|
    US15/117,756| US10745530B2|2014-02-12|2015-02-11|Sizing composition for reinforcing fibres and applications thereof|
    EP15706709.1A| EP3105277B1|2014-02-12|2015-02-11|Sizing composition for reinforcing fibres and applications thereof|
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