Synthesis of activated vitrimer epoxy anhydride resin

Abstract

A method of manufacturing an activated vitrimer epoxy anhydride resin for reshaping composite material parts comprising an epoxy anhydride resin and glass fibers, the manufacturing method comprising the following steps: a) preparing a solution from a mixture of three precursor components comprising a polyanhydride, an amino alcohol, a polyepoxy, and a solvent, b) stirring the solution, c) evaporating the solvent to obtain a precursor mixture of the activated vitrimer epoxy anhydride resin, and d) crosslinking by applying a heat treatment to obtain the activated vitrimer epoxy anhydride resin. Figure 1

Description

Title of the invention: Synthesis of activated vitrimer epoxy anhydride resin

[0001] The present invention relates to the reshaping of waste composite material parts based on glass fibers and epoxy-anhydride resin. In particular, the invention relates to an activated vitrimer epoxy-anhydride resin, intended to facilitate the reshaping of these composite material parts. It further provides a method for manufacturing such a resin and a method for reshaping said composite material parts.

[0002] Composite materials of fiberglass and epoxy resin are used in particular as structural materials to replace metals and allow significant weight reduction for a wide range of applications: sport (cycles, board sports), transport (structure of cars, trains), aerospace (structure of airplanes, space shuttles). These systems consist of a thermosetting polymer resin, crosslinked during the shaping of the material, and a fiber armor, which can be of variable nature (mainly carbon fibers and glass fibers) and organization (woven according to different models, non-woven).

[0003] These thermosetting resins have high mechanical performance and chemical resistance, thanks in particular to the high crosslinking of the network. However, this aspect prohibits any recycling other than incineration, because these crosslinked networks cannot be melted or solubilized, preventing the use of conventional recycling techniques.

[0004] The use of reversible chemistries for the synthesis and use of reversible networks constitutes a new field of research in polymer engineering. The use of reversible networks makes it possible to overcome the lack of recyclability of thermosets. Research in this field is rich in innovations and many covalent and reversible chemical systems have been studied.

[0005] In the field of epoxy resins, there are three main types: epoxy-amines, epoxy-vinylester and epoxy-anhydrides (or epoxy-esters). Among them, only epoxy-anhydride resins have properties of reversible chemistry by nature, thanks to available ester functions and hydroxyl groups, which makes it possible to envisage recycling this resin by transforming it into vitrimer. Indeed, the ester functions, in the presence of free reactive sites and under certain conditions (by heating for example), can be exchanged step by step via a transesterification reaction, and result in a topological reorganization of the material. at the molecular level (refer to [Fig.2] below). When the frequency of these exchanges is high enough, the stressing of the material gives rise to deformation at the macroscopic level, which can be used to repair or change the shape of parts made of said material. This opens the door to the recycling of resins in damaged or end-of-life composite material parts.

[0006] The use of transesterification in epoxy-polyester resins has already been the subject of publications and numerous studies. Current work is mainly aimed at improving this system on several points: the speed and temperature at which the exchanges take place, as well as the thermomechanical performance of the materials and their resistance to water and other solvents. Indeed, the introduction of reversible chemical bonds brings new problems. These bonds can be less stable, the materials incorporating them do not have the same properties depending on the temperature or in the presence of certain solvents. Also, the speed of reshaping of the material is directly linked to the effectiveness of the reversible chemistry used. The general objective is to obtain materials that perform well under normal conditions of use but that reshape quickly.

[0007] For this, activators and catalysts are introduced into these materials to accelerate the exchange chemistry. The first generation of vitrimer epoxy esters described in the literature sees the exchange reaction activated by activators mixed into the polymer in the manner of an additive. But the quantity required is generally around 5 to 10% by mass, which can cause losses in the performance of the material. In addition, since these activator molecules are free in the material, they can, like many other additives used in the plastics industry, be led to migrate out of the material, leading to losses in performance as well as exposure of users and the environment to undesirable or even dangerous molecules.

[0008] The second generation of vitrimeric epoxy esters known to date consists of the integration of molecules directly into the polymer structure, in a covalent manner. However, even if improvements are observed with this technique, the reagents used still need to be optimized to lead to resins with more relevant thermomechanical properties as well as higher reshaping kinetics.

[0009] One of the aims of the present invention is to overcome at least one of the aforementioned drawbacks. To this end, the invention provides a method for manufacturing an activated vitrimer epoxy-anhydride resin, intended for the reshaping of parts made of composite materials comprising an epoxy-anhydride resin and glass fibers, the manufacturing method comprising the following steps: - a) preparation of a solution from a mixture of three precursor components comprising a polyanhydride, an aminoalcohol, a polyepoxy and a solvent, - b) stirring the solution, - c) evaporation of the solvent so as to obtain a precursor mixture of the activated epoxy-vitrimer anhydride resin, and - d) crosslinking by applying a heat treatment so as to obtain the activated vitrimer epoxy anhydride resin.

[0010] Thus, the process of the invention leads to the production of an activated vitrimer epoxy-anhydride resin in that it contains judiciously chosen functions, in a determined conformation making it possible to activate the kinetics of ester exchanges and rapid reshaping. Indeed, the process consists of the advantageous use of a selection of three chemical species: a poly-epoxy, a poly-anhydride and an amino alcohol. These three species are capable of reacting with each other to form a covalent crosslinked network comprising a large number of esters. In addition, the use of a poly-anhydride allows the formation of carboxylic acid in the beta position relative to the ester (or in the ortho position when the anhydride is arranged on an aromatic cycle), which increases the kinetics of ester exchange.The use of an amino alcohol also allows the formation of an amine in the beta position relative to the ester and this configuration also increases the kinetics of ester exchange. Finally, the use of a polyepoxy allows the formation of hydroxyl groups during the crosslinking reaction. These OH groups act as free reactive sites during ester exchanges. The combination of carboxylic acid, tertiary amine and hydroxyl groups near the ester allows for very rapid exchange chemistry and very efficient reformatting.

[0011] Furthermore, the use of poly-anhydride instead of anhydride and a poly-epoxy as conventionally used makes it possible to obtain a resin having a higher glass transition temperature than that of already existing vitrimeric epoxy resins. In addition, the combination of reagents makes it possible to form stable covalent bonds making it possible to do without the addition of an additional catalyst which could migrate outside the material.

[0012] The term "poly-epoxy" is understood herein to mean a molecule comprising at least two epoxy functions. The term "poly-anhydride" is understood herein to mean a molecule comprising at least two anhydride functions.

[0013] According to one possibility, the precursor mixture of the activated vitrimer epoxy anhydride resin is a mixture of the three precursor components having partially crosslinked.

[0014] Thus, once said resin has been crosslinked and hardened, it can be either ground or hot-compressed directly to form plates. The resin, in the form of plates or ground, can be used in a mixture with waste composite material parts in order to obtain a recycled composite by compression and heating and re-shaping.

[0015] According to one arrangement, the polyanhydride is selected from aromatic components. This contributes to generating a high stress in the molecule which leads to a high glass transition temperature.

[0016] According to one possibility, the polyanhydride is selected from dianhydrides and trianhydrides, such as pyromellitic acid dianhydride (PDMA), bisphenol A dianhydride (BPA), 3,3'4,4'-benzophenonetetracarboxylic dianhydride (BTDA), mellitic anhydride, or a mixture of these polyanhydrides.

[0017] According to one possibility, the polyepoxy is selected from bisphenol A diglycidyl ether (DGEBA), Tris(4-hydroxyphenyl)methane triglycidyl ether, 4,4'-Methylenebis(N,N-diglycidylaniline), N,N-Diglycidyl-4-glycidyloxyaniline, 1,4-butanediol diglycidyl ether, and Bisphenol F diglycidyl ether or a mixture of these compounds.

[0018] According to one arrangement, the polyepoxy is chosen so as to have functions and a geometric conformation close to that of the epoxy resin of the composite material to be reshaped, so as to have similar properties and facilitate interactions.

[0019] According to one possibility, the amino alcohol is chosen from tertiary amines comprising at least two hydroxyl functions, such as triethanolamine (TEthA), diethanolmethylamine (DEthA), tetrahydroxyethylenediamine (THEED) or a mixture of these amines. Tertiary amines are preferred because the presence of primary (NH2) or secondary (NH) amine allows the addition reaction of these amines with the epoxy and the formation of permanent non-reversible bonds, which in this case are parasitic reactions because they are non-exchangeable.

[0020] According to one embodiment, step a) comprises first diluting the polyanhydride in a liquid monoanhydride, such as hexahydro-4-methylphthalic anhydride (HHMPA), methyl nadic anhydride (MNA) or a mixture of these monoanhydrides.

[0021] According to one arrangement, crosslinking step d) comprises the application of a heat treatment at a temperature between 110°C and 140°C, in particular between 120°C and 130°C. This temperature is determined to optimize the crosslinking speed and minimize parasitic reactions.

[0022] According to one possibility, crosslinking step d) comprises the application of a vacuum, in particular a pressure less than or equal to -0.2 bar, and for example a pressure less than or equal to -0.5 bar.

[0023] According to one possibility, the molar ratio in the solution prepared in step a) of the anhydride, epoxide and hydroxyl functions are in a range between 1:1:1 and 3:1:1, and in particular a molar ratio of approximately 2:1:1. This configuration makes it possible to ensure that a maximum of anhydride functions are modified into ester to promote exchanges and reshaping with high kinetics.

[0024] According to a second aspect, the invention provides an activated vitrimer epoxy anhydride resin, intended for the reshaping of composite material parts comprising an epoxy anhydride resin and glass fibers, the activated vitrimer epoxy anhydride resin comprising a covalent crosslinked network comprising ester functions, carboxylic acid functions, hydroxyl functions and tertiary amine functions making it possible to activate the kinetics of the exchange reactions, the activated vitrimer epoxy anhydride resin originating from the crosslinking of at least one polyanhydride so as to generate a maximum of esters in the resin. The presence of these functions makes it possible to carry out activated trans-esterification reactions, resulting in an easy and rapid topological reorganization of the material and the possibility of also rapid reshaping on a macroscopic scale.

[0025] According to one arrangement, the activated vitrimer epoxy-anhydride resin comes from the reaction between at least one poly-epoxy, at least one poly-anhydride and at least one amino alcohol.

[0026] According to one possibility, said activated vitrimer epoxy anhydride resin has a glass transition temperature Tg greater than or equal to 130°C, in particular between 130°C and 250°C, for example between 150°C and 200°C. This high temperature is obtained in particular by using a polyanhydride with a constrained chemical structure, solid at room temperature and having a high melting temperature. The resulting characteristics guarantee the possibility of reshaping said resin itself, or a part made of composite material which would be modified by the integration of said resin, allowing a higher operating temperature of the new part than that of the vitrimer epoxy anhydrides known to date, which broadens their field of application.

[0027] According to one arrangement, the activated vitrimeric epoxy anhydride resin comprises a majority of carboxylic acid functions arranged in the beta position of the ester functions or in the ortho position when the carboxylic acid functions and the ester functions are substituents of aromatic rings, a majority of tertiary amine functions are arranged in the beta position of the ester functions and a majority of hydroxyl functions are arranged in the beta position of the ester functions. Thus, said carboxylic acid functions and said tertiary amine functions act as activators of the ester exchange kinetics and the hydroxyl functions act as free reactive sites in the ester exchanges. This allows a double activation or dual catalysis of very rapid exchange chemistry and optimal reshaping. This activated vitrimer epoxy-anhydride resin has characteristics that enable efficient and rapid reshaping recycling processing of epoxy-anhydride resin composite material parts as will be described below.

[0028] According to a third aspect, the invention proposes a method for recycling parts made of composite material based on epoxy-anhydride resin and glass fibers, the method comprising the steps of:

[0029] m) providing an activated vitrimer epoxy anhydride resin as previously described, the activated vitrimer epoxy anhydride resin being in powder form,

[0030] n) providing particles from at least one piece of composite material based on glass fibers in an epoxy-anhydride resin,

[0031] o) mixing the activated vitrimer epoxy anhydride resin powder and the composite material particles so as to obtain a homogeneous mixture,

[0032] p) placing the homogeneous mixture in a mold previously heated to a temperature Tm greater than or equal to the glass transition temperature Tg of the activated vitrimer epoxy anhydride resin, such as a temperature Tm greater than or equal to 130°C, in particular a temperature between 130°C and 250°C, for example 200°C, and

[0033] q) applying a pressure greater than or equal to 60 bars, in particular a pressure of between 60 and 80 bars, and for example approximately 70 bars, for a few tens of minutes, in particular between 20 and 30 min, at a temperature greater than or equal to the glass transition temperature Tg of the activated epoxy-anhydride vitrimer resin, so as to reshape the composite material.

[0034] This method thus advantageously uses the activated vitrimer resin of the invention for a reaction with epoxy-anhydride / glass fiber composite materials giving rise to the formation of a new covalent network allowing the transformation of waste into a composite material into a material that is intrinsically recyclable thereafter. Indeed, the epoxy-anhydride vitrimer resin present in the composite material is capable of the same chemical exchanges as the resin of the invention, but with much lower kinetics because these reactions are not activated in this case. When they are mixed and then hot compressed, the two resin networks form, via the trans-esterification reaction, a single, crosslinked network. This makes it possible to integrate the composite material at the end of its life into a recyclable vitrimer resin, giving rise to a material that is itself recyclable.Note that the temperature applied in step q) is independent of the preheating temperature of the mold.

[0035] According to other characteristics, the manufacturing method of the invention comprises one or more of the following optional characteristics considered alone or in combination: - The number of anhydride functions is preferably less than or equal to the cumulative number of epoxide and hydroxyl functions in the solution of step a). - The solvent used in step a) of preparing a solution is chosen from polar organic solvents such as THF, anisole, dimethylacetamide, dimethylformamide, DMSO, acetonitrile, acetone, ethyl acetate, etc. - Step b) of stirring the solution is carried out between room temperature and 50°C. - Step c) of evaporation of the solvent is carried out at a temperature between room temperature and approximately 60°C so as to compensate for the viscosity of the resin precursor mixture. - The crosslinking treatment of step d) is carried out for several hours, in particular for 10 to 20 hours, for example 15 hours.

[0036] Other characteristics and advantages will appear on reading the detailed description below, of a non-limiting example of implementation, made with reference to the appended figures in which:

[0037] [Fig. 1] illustrates the reaction scheme between the three components leading to the activated vitrimer epoxy anhydride resin according to one embodiment of the invention.

[0038] [Fig.2] represents a schematic view of the principle of transesterification which is applied in the invention.

[0039] [Fig.3] shows examples of poly-anhydride, used as one of the three components of the invention.

[0040] [Fig.4] represents examples of amino alcohol, used as one of the three components of the invention.

[0041] [Fig.5] represents an example of poly-epoxy, used as one of the three components of the invention.

[0042] [Fig.6] illustrates the reaction scheme between a polyanhydride, an alcohol and an epoxy according to the invention.

[0043] [Fig.7] illustrates the reaction scheme between a polyanhydride and an amino alcohol according to the invention.

[0044] As illustrated in [Fig.l], the present invention proposes the synthesis of an activated anhydride epoxy-vitrimer resin from three specific components, allowing the increase of the kinetics of a transesterification reaction as illustrated in [Fig.2]. To do this, the method of the invention proposes to form a reaction mixture from three solutions of precursor components. Thus, in a In the first container, a first solution is prepared from 1 g of pyromellitic acid dianhydride PDMA in 40 ml of THF ([Fig.2]). In a second container, a second solution is prepared from 0.817 g of DGBEA resin ([Fig.4]) in 40 ml of THF and in a third container, a third solution is prepared from 0.228 g of triethanolamine TEthA ([Fig.3]) in 40 ml of THF. The three solutions are mixed to prepare the solution according to step a) which is stirred at room temperature according to step b) for a fairly short time (between 30 seconds and 2 minutes) to prevent the solution from solidifying in the container of step b). The molar ratio of the anhydride, epoxide and hydroxyl functions is approximately 2:1:1. Then, the THF solvent is evaporated into the open air according to step c) so as to obtain a precursor mixture of said final resin in which the three components are pre-crosslinked.The mixture being viscous, it is placed in an oven heated to 60°C so as to complete the evaporation of the solvent. Then a heat treatment according to step d) is applied at 130°C for 15 hours under a pressure of less than 1 bar so as to finalize the crosslinking and obtain the activated epoxy-vitrimer anhydride resin ([Fig.l]). Said activated resin is formed of a covalent network comprising determined functions and a specific conformation allowing a double activation of the exchange reactions so as to increase the reshaping kinetics. In particular, said activated resin comprises carboxylic acid functions arranged in the ortho position of the ester functions when the carboxylic acid functions and the ester functions are substituents of an aromatic cycle (refer to [Fig.l] and to the molecules Ia and Id respectively in Figures 6 and 7), tertiary amine functions arranged in the beta position of ester functions (refer to [Fig.l] and to the molecules Id in [Fig.7]) so that the exchange sites are doubly activated. Hydroxyl functions are also present on the covalent network and act as free reactive sites during ester exchanges.

[0045] According to other embodiments of the invention, the polyanhydride component is chosen from BPA, BTDA, mellitic anhydride, or a mixture of these compounds ([Fig.2]). The aminoalcohol component is chosen from tertiary amines comprising at least two hydroxyl functions, such as DEthA, THEED or a mixture of these amines.

[0046] According to another embodiment of the invention, the polyanhydride is dissolved in a monoanhydride ([Fig.6]). THF can be added to this solution depending on the solubility characteristics of the polyanhydride.

[0047] The invention also proposes a method for recycling parts made of composite material based on epoxy-anhydride resin and glass fibers by integrating said activated resin (not shown). An exemplary embodiment of the recycling method according to the invention firstly comprises the supply of 60g of a resin activated vitrimer epoxy anhydride as previously described, previously ground if necessary to present a powder form (step m). To this powder is added 50g of particles from parts to be recycled of said composite material (step n). Once a homogeneous mixture is obtained following vigorous stirring (step o), it is placed in a mold previously heated to Tm (180°C-step p). The assembly is then pressed with a pressure of 70 bars for 30 min at 180°C (step q). The reshaped part is then demolded. It is formed from a composite material comprising glass fibers and an epoxy anhydride resin comprising a covalent network in which the activated vitrimer epoxy anhydride resin is integrated, so that it can be quickly reshaped or locally repaired several times, without adding new material, by the same compression / heating process.

[0048] Thus, the present invention uses the properties of vitrimer resins and judiciously chooses components entering into the composition of the activated resin to improve the exchange kinetics, promote the reshaping, repair and recyclability of parts made of composite materials, without degradation of its mechanical properties of the composite materials nor the resistance to water, solvent, etc., while increasing the glass transition temperature and thus the field of application of these parts.

Claims

Claims

1. A method of manufacturing an activated vitrimer epoxy anhydride resin, intended for reshaping composite material parts comprising an epoxy anhydride resin and glass fibers, the manufacturing method comprising the following steps: - a) preparing a solution from a mixture of three precursor components comprising a polyanhydride, an amino alcohol, a polyepoxy and a solvent, - b) stirring the solution, - c) evaporating the solvent so as to obtain a precursor mixture of the activated vitrimer epoxy anhydride resin, and - d) crosslinking by applying a heat treatment so as to obtain the activated vitrimer epoxy anhydride resin.

2. A manufacturing method according to claim 1, wherein the polyanhydride is selected from dianhydrides and trianhydrides, such as pyromellitic acid dianhydride (PDMA), bisphenol A dianhydride (BPA), 3,3'4,4'-benzophenonetetracarboxylic dianhydride (BTDA), mellitic anhydride or a mixture of these polyanhydrides.

3. A manufacturing method according to claim 1 or 2, wherein the polyepoxy is selected from bisphenol A diglycidyl ether (DGEBA), Tris(4-hydroxyphenyl)methane triglycidyl ether, 4,4'-Methylenebis(N,N-diglycidylaniline), N,N-Diglycidyl-4-glycidyloxyaniline, 1,4-butanediol diglycidyl ether, and Bisphenol F diglycidyl ether or a mixture of these compounds.

4. Manufacturing process according to one of claims 1 to 3, in which the amino alcohol is chosen from tertiary amines comprising at least two hydroxyl functions, such as triethanolamine (TEthA), diethanolmethylamine (DEthA), tetrahydroxyethylenediamine (THEED) or a mixture of these amines.

5. Manufacturing process according to one of claims 1 to 4, in which step a) comprises first diluting the polyanhydride in a liquid monoanhydride, such as hexahydro-4-methylphthalic anhydride (HHMPA), methyl nadic anhydride (MNA) or a mixture of these monoanhydrides.

6. Manufacturing method according to one of claims 1 to 5, in which step d) of crosslinking comprises the application of a heat treatment at a temperature between 110°C and 140°C.

7. Manufacturing process according to one of claims 1 to 6, in which the molar ratio in the solution prepared in step a) of the anhydride, epoxide and hydroxyl functions are in a range between 1:1:1 and 3:1:1, and in particular a molar ratio of approximately 2:1:

1.

8. Activated vitrimer epoxy-anhydride resin, intended for the reshaping of parts made of composite material comprising an epoxy-anhydride resin and glass fibers, the activated epoxy-anhydride resin comprising a covalent crosslinked network comprising ester functions, carboxylic acid functions, hydroxyl functions and tertiary amine functions making it possible to activate the kinetics of the exchange reactions, the activated epoxy-anhydride resin originating from the crosslinking of at least one poly-anhydride so as to generate a maximum of esters in the resin.

9. The activated vitrimeric epoxy anhydride resin of claim 8, wherein a majority of carboxylic acid functions are arranged in the beta position of the ester functions or in the ortho position when the carboxylic acid functions and the ester functions are substituents of an aromatic ring, a majority of tertiary amine functions are arranged in the beta position of the ester functions and a majority of hydroxyl functions are arranged in the beta position of the ester functions.

10. A method for recycling parts made of composite material based on epoxy-anhydride resin and glass fibers, the method comprising the steps of: m) providing an activated vitrimer epoxy-anhydride resin according to one of claims 8 or 9 and / or manufactured according to the manufacturing method of claims 1 to 7, the activated vitrimer epoxy-anhydride resin being in powder form, n) providing particles from at least one part made of composite material based on glass fibers in an epoxy-anhydride resin, o) mixing the activated vitrimer epoxy-anhydride resin powder and the particles made of composite material so as to obtain a homogeneous mixture, p) placing the homogeneous mixture in a mold previously heated to a temperature Tm higher than the glass transition temperature Tg of the activated epoxy-vitrimer anhydride resin, and q) applying a pressure greater than or equal to 60 bars, for a few tens of minutes, at a temperature greater than or equal to the glass transition temperature Tg of the activated epoxy-vitrimer anhydride resin so as to reshape the composite material.