FABRICATION OF BENZOXAZINE FUNCTIONALIZED PARTICLES

Abstract

A method includes adding particles to an alkaline solution, stirring the solution to cause the particles to acquire hydroxyl groups producing activated particles, dispersing the activated particles into a solvent solution, adding acetylene benzoxazine into the solvent solution, mixing the solvent solution, removing the solvent from the solvent solution to produce acetylene-benzoxazine functionalized particles, and drying the acetylene-benzoxazine functionalized particles. A composition of matter has acetylene-benzoxazine functionalized particles dispersed in a resin.

Claims

1. A method, comprising: adding particles to an alkaline solution; stirring the solution to cause the particles to acquire hydroxyl groups producing activated particles; dispersing the activated particles into a solvent solution; adding acetylene benzoxazine into the solvent solution; mixing the solvent solution; removing the solvent from the solvent solution to produce acetylene-benzoxazine functionalized particles; and drying the acetylene-benzoxazine functionalized particles.

2. The method as claimed in claim 1, wherein the particles comprises silicon carbide particles and the method further comprises annealing the silicon carbide particles prior to putting the activated particles in the alkaline solution.

3. The method as claimed in claim 1, wherein stirring the solution further comprises washing the activated particles and drying the activated particles prior to dispersing the activated particles into the solvent solution.

4. The method as claimed in claim 1, wherein dispersing the activated particles into a solvent solution comprises dispersing the activated particles into the solvent solution with a catalyst.

5. The method as claimed in claim 4, wherein dispersing the activated particles into the solvent solution with the catalyst comprises dispersing the activated particles into the solvent solution with at least one Lewis acid as the catalyst.

6. The method as claimed in claim 5, wherein the Lews acid comprises one or more of FeCl.sub.3, FeCl.sub.3/AgSbF.sub.6, FeF.sub.3, FeBr.sub.3, AlCl.sub.3, BF.sub.3, BBr.sub.3, SnCl.sub.4, SnF.sub.4, PF.sub.5, PCl.sub.5, ZnCl.sub.2, BeCl.sub.2, SiF.sub.4, SiCl.sub.4, SbCl.sub.5, NbCl.sub.5, FeCl.sub.3x(H.sub.2O).sub.6, and ZnCl.sub.2xH.sub.2O.

7. The method as claimed in claim 1, wherein removing the solvent comprises separating the benzoxazine functionalized particles by one of centrifugation or filtration, and washing the benzoxazine functionalized particles.

8. The method as claimed in claim 1, wherein the particles are selected from the group consisting of: silicon carbide, silica, clays, amorphous carbon, crystalline carbon, carbon black, titania, MgO, GO, SiO2, Al.sub.2O.sub.3, Fe.sub.3O.sub.4), TiO.sub.2, CeO.sub.2, ZnO, Cu.sub.2O.sub.3, NiO, CdO, Ag.sub.2O, MoO.sub.3, WO.sub.3, SnO.sub.2, CuO, Cr.sub.2O.sub.3, In.sub.2O.sub.3, hydroxyapatite, BN, BC.sub.4, metal oxides or compounds that can be turned into metal oxides with application of a treatment, and carbon nanotubes.

9. The method as claimed in claim 1, wherein the solvent is one or more selected from the group consisting of: dichloromethane, chloroform, 1,1-dichloroethane, 1,2-dichloroethane, trichloro ethane, tetrahydrofuran, dioxane, ethylene glycol ethers, dimethyl glycol ethers, ethyl glycol ethers, diethylene glycol, and triethylene glycol

10. The method as claimed in claim 1, wherein the particles comprise silicon carbide and the method further comprises: mixing a mixture of the acetylene-benzoxazine silicon carbide particles with a benzoxazine monomer; initiating polymerization of the benzoxazine monomer in the mixture to create a resin having the silicon carbide particles dispersed within; and curing the resin.

11. The method as claimed in claim 10, wherein initiating polymerization comprises adding a radical initiator to the mixture.

12. The method as claimed in claim 11, wherein initiating polymerization comprises heating the mixture to a first temperature, and curing the resin comprises heating the resin to a second temperature higher than the first temperature.

13. The method as claimed in claim 10, wherein initiating polymerization comprises heating the mixture to a first temperature sufficient to promote benzoxazine polymerization and then heating the mixture to a second temperature sufficient to promote acetylene polymerization.

14. The method as claimed in claim 10, further comprising forming an object from the resin prior to curing.

15. The method as claimed in claim 14, further comprising pyrolizing the object to produce a ceramic object.

16. The method as claimed in claim 14, wherein forming the object comprises three-dimensional printing the mixture.

17. The method as claimed in claim 16, wherein three-dimensional printing comprises one of extrusion, indirect powder bed sintering, or direct powder bed sintering.

18. The method as claimed in claim 10, wherein the benzoxazine monomer comprises one of acetylene-benzoxazines, vinly benoxazines, allyl benzoxazines, propargyl benzoxazines, and furan-funtionalized benzoxazines.

19. A composition of matter, comprising acetylene-benzoxazine functionalized particles dispersed in a resin.

20. The composition of matter of claim 18, wherein the functionalized particles comprise SiC and the resin comprises a benzoxazine resin

21. The composition of matter of claim 19, wherein the resin forms an object.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0009] FIGS. 1 and 2 show alternative embodiments of a method of fabrication of benzoxazine functionalized particles.

[0010] FIG. 3 shows a diagram of an embodiment of a process of particle functionalization with acetylene-benzoxazine.

[0011] FIG. 4 shows examples of acetylene-benzoxazines suitable for the embodiments.

[0012] FIG. 5 shows an example of an allyl-containing benzoxazine suitable for use as a resin in the embodiments.

[0013] FIG. 6 shows an example of a furan-containing benzoxazine suitable for use as a resin in the embodiments.

DETAILED DESCRIPTION OF THE EMBODIMENTS

[0014] The embodiments here involve a method of fabrication of benzoxazine functionalized particles by reacting hydroxyl activated particles with an acetylene-containing benzoxazine. The embodiments also include a method for fabrication of acetylene-benzoxazine functionalized SiC particles and nanoparticles. The embodiments here also include composite formulations comprising acetylene-functionalized nanoparticles dispersed in a benzoxazine resin. In one embodiment, the benzoxazine resin is an acetylene-functionalized benzoxazine. In another embodiment, it is a furan-functionalized benzoxazine. In still another embodiment, it is a vinyl-functionalized benzoxazine such as propargyl-benzoxazine. The embodiments may include an object made of the composite formulation above, and ceramic made by pyrolyzing the object.

[0015] Many inorganic particles already have hydroxyl (OH) groups onto their surface. Examples of such particles include SiO.sub.2, Al.sub.2O.sub.3, Fe.sub.3O.sub.4, TiO.sub.2, and others. SiC particles, on the other hand, have no OH groups or have only very small amount, which prevents them from reacting with the acetylene group from the benzoxazine molecule. The method for fabrication of functionalized SiC nanoparticles requires a first step to introduce OH groups onto their surface. One suitable process [S. Alekseev, E. Shamatulskaya, M. Volvach, S. Gryn, D. Korytko, I. Bezverkhyy, V. Iablokov, V. Lysenko, Size and Surface Chemistry Tuning of Silicon Carbide Nanoparticles, Langmuir 2017, 33, 13561-13571] consists in first, thermal oxidation of the SiC nanoparticle surface to produce an oxide layer onto the surface of these particles. The process comprises annealing in air with a heating ramp with a temperature comprising a range from 0.1° C./min to 100° C./min, and kept for a desired time comprising a range from 1 min to 24 hours, at a temperature comprising a range from 300° C. to about 1000° C. In the second step, the oxide layer is hydrolyzed to form hydroxide group by stirring the oxide surface functionalized particles in an alkaline solution, followed by drying in air. The alkaline solution may comprise KOH, NaOH, CsOH dissolved in water in a concentration from about 0.1 M to 20 M. The particles are washed with water and dried. Using steam, plain water or any water containing solution or spray or any form instead of alkaline solution can also hydrolyze the oxide layer to hydroxide group.

[0016] The next step comprises a chemical reaction of the OH groups onto the surface of the particles with acetylene-benzoxazine. A process for a coupling reaction of organic alcohols with acetylenes has been described in solution previously, as in [L. R. Jefferies et al., Alcohols as electrophiles: iron-catalyzed Ritter reaction and alcohol addition to alkynes. Tetrahedron, 2014. 70(27): p. 4204-4207].

[0017] Unlike these references, the embodiments here provide particle functionalization, instead of organic molecules coupling, development of a process suitable for acetylene-benzoxazine, and a process for fabrication of benzoxazine functionalized SiC.

[0018] In one embodiment, acetylene-benzoxazine functionalized particles dispersed in acetylene-benzoxazine are fabricated in a one-step process. This is advantageous because it eliminates the need to separate and purify particles, then remixing them with benzoxazine monomer. Acetylene-benzoxazine precursors are advantageous because they produce high yield char upon pyrolysis. The process has been disclosed in U.S. patent application Ser. No. 17/582,901, filed Jan. 24, 2022, which is incorporated by reference herein in its entirety.

[0019] In a more general embodiment, shown in FIG. 1 the particles are functionalized at 10 typically by stirring in an alkaline solution to cause the particles to acquire a hydroxyl (OH) group. The OH functionalized particles are then dispersed into a solvent at 12. Acetylene benzoxazine is added at 14, possibly with a catalyst and then mixed. The mixture is stirred at 16, possibly under reflux for a period of time sufficient to maximize the functionalization. The particles are separated from solvent and washed at 18, then dried at 20.

[0020] A more specific embodiment is shown in FIG. 2. The particles are functionalized with an acetylene-benzoxazine monomer, purified and then are dispersed in a solvent and a benzoxazine monomer. This may involve annealing the SiC particles at 30. The annealed particles are cooled at 32. The cooled particle are stirred in an alkaline solution at 34, then are washed with water at 36 and then dried at 40, to produce particles activated with OH groups (SiC—OH). The particles may then be dispersed with stirring into a solvent, then a catalyst at 42. The catalyst may comprise a Lewis acid or a mixture of more than one Lewis acid is added and stirred to solubilize the Lewis acid in the solvent. Acetylene benzoxazine is then added. The benzoxazine then dissolves while the solution undergoes stirring, and the mixture is heated above the boiling point of the solvent to achieve a solvent reflux at 44. The mixture is stirred under reflux for a period of time sufficient to maximize the functionalization. After cooling down at 46, the particles are separated from solvent by centrifugation or by filtration at 48. The particles are washed with a solvent to recover the unreacted or the excess of acetylene-benzoxazine, further washed with water to remove the inorganic products at 50 and dried at 52.

[0021] The attachment of the acetylene-benzoxazine takes place by chemical coupling that produces a ketone group. The process may require a Lewis acid catalyst, such as ferric chloride (FeCl.sub.3) or ferric chloride/silver hexafluoroantimonate (FeCl.sub.3/AgSbF.sub.6). Other Lewis acid catalysts may also catalyze the particle functionalization reaction including ferric fluoride (FeF.sub.3), ferric bromide (FeBr.sub.3), aluminum chloride (AlCl.sub.3), boron fluoride (BF.sub.3), boron bromide ((BBr.sub.3), tin tetrachloride (SnCl.sub.4), tin (IV) fluoride (SnF.sub.4), phosphorous pentafluoride (PF.sub.5), phosphorous pentachloride (PCl.sub.5), zinc chloride (ZnCl.sub.2), beryllium chloride (BeCl.sub.2), silicon tetrafluoride (SiF.sub.4), silicon tetrachloride (SiCl.sub.4), antimony pentachloride (SbCl.sub.5), and niobium pentachloride (NbCl.sub.5). In some embodiments, the Lewis acids may be hydrated, such as FeCl.sub.3x(H.sub.2O).sub.6 and ZnCl.sub.2xH.sub.2O. In other embodiments, Lewis acids can act in synergy with salts of superacids. Example of suitable salts of superacids include antimony halide salts: AgSbF.sub.6; NaSbF.sub.6; Cu(SbF.sub.6).sub.2; and NH.sub.4SbF.sub.6; triflates: NaO.sub.3SCF.sub.3; AgO.sub.3SCF.sub.3; Yb(O.sub.3SCF.sub.3).sub.3; fluorosulfonic acid salts: NaSO.sub.3F; LiSO.sub.3F; Be(SO.sub.3F).sub.2; NH.sub.4SO.sub.3F; N(CH.sub.3).sub.4SO.sub.3F; and Al(SO.sub.3F).sub.3; chlorosulfonic acid salts: NaSO.sub.3Cl; LiSO.sub.3Cl; Be(SO.sub.3Cl).sub.2; NH.sub.4SO.sub.3Cl; N(CH.sub.3).sub.4SO.sub.3Cl; and Al(SO.sub.3Cl).sub.3; and carborane acid salts: Na(CHB.sub.11X.sub.11); Li(CHB.sub.11X.sub.11); and Cs(CHB.sub.11X.sub.11) wherein X is a halogen such as Cl and F. As an example a system containing a mixture of FeCl.sub.3x(H.sub.2O).sub.6+AgSbF.sub.6 may be more efficient than the FeCl.sub.3x(H2O).sub.6 alone.

[0022] Suitable solvents include dichloromethane, chloroform, 1,1-dichloroethane, 1,2-dichloroethane, trichloro ethane, tetrahydrofuran, dioxane, ethylene glycol ethers such as dimethyl and ethyl glycol ethers and higher molecular weight ether of other diols such as diethylene or triethylene glycol. Higher boiling solvents may be beneficial for accelerating the reaction rate, therefore decreasing the reaction time. Reaction time may differ for different solvents, can be in a range from 1 hour to 24 hours or more. The reaction temperature may comprise a range from 40° C. to 250° C.

[0023] FIG. 3 shows an embodiment of the chemical functionalization process. Chemical reaction of the OH-functionalized particle on the left side results in a particle being functionalized with acetylene-benzoxazine on the right.

[0024] FIG. 4 shows various examples of acetylene-benzoxazines suitable for the embodiments here.

[0025] While the embodiments described in detail here involve specifics to SiC nanoparticles, the process can be extended to other particles and nanoparticles that contain hydroxyl groups (—OH) onto their surface. Example of other particles suitable for this process include: silica, clays, amorphous or crystalline carbon included carbon black, titania, magnesium oxide (MgO), graphene oxide (GO), silicon dioxide (SiO.sub.2), aluminum oxide (Al.sub.2O.sub.3), ferrous oxide (Fe.sub.3O.sub.4), titanium dioxide (TiO.sub.2), cesium dioxide (CeO.sub.2), zinc oxide (ZnO), copper (III) oxide (Cu.sub.2O.sub.3), niobium oxide (NiO), cadmium oxide (CdO), silver dioxide (Ag.sub.2O), molybdenum trioxide (MoO.sub.3), tri-tungsten(VI) oxide (WO.sub.3), tin(IV) oxide (SnO.sub.2), cupric oxide (CuO), chromium oxide(Cr.sub.2O.sub.3), indium oxide (In.sub.2O.sub.3), hydroxyapatite, boron nitride (BN), boron carbide (BC.sub.4), and carbon nanotubes, among others. The particles may comprise metal oxides, or any particle that can be turned into a metal oxide by application of a treatment, such as thermal, electrical, plasma, and microwave. The particles may have any shape, including one-dimensional, two-dimensional, three-dimensional, and random shapes. The functionalized particles may be of any size, ranging from 1 nm to 5 mm.

[0026] The particle loading may occur in a range from 1 v % to 60 v %. For ceramic applications, higher content (40 v %-60 v %) has advantages because it increases the ceramic yield and reduces the voids.

[0027] In one embodiment, formulations with acetylene-benzoxazine-SiC particles in a benzoxazine resin are prepared by mixing them in a benzoxazine monomer, typically with high shear mixers. While in principle, the functionalized particles can be dispersed in any benzoxazine resin, of particular interest are those benzoxazine resins that can bond with the acetylene groups present onto the surface of the acetylene-benzoxazine-SiC particles. Suitable benzoxazines include acetylene-benzoxazines such as those shown in FIG. 4, because they can bond to the particles by coupling between the acetylene groups present onto particle and the acetylene group present in the benzoxazine resin, by radical polymerization. This embodiment is advantageous because it allows for radical polymerization of the acetylene groups to produce dense and mechanically strong SiC/benzoxazine composites upon curing. In addition, it may increase the high-temperature stability of the cured object made with these formulations. A radical initiator may be present in the formulation, such as a thermal radical initiator that initiates a radical polymerization by dissociation into radicals when heated. Suitable initiators include organic peroxides, AIBN (Azobisisobutyronitrile) and the like.

[0028] Other suitable benzoxazine with radical polymerizable groups include vinyl and allyl containing benzoxazines. FIG. 5 shows an example of such a group. Other suitable resin with functional groups that may react with the acetylene group present onto the surface of the acetylene-benzoxazine-SiC particles include furan-functionalized benzoxazines. FIG. 5 shows an example. Furan bonds to acetylene by Diels-Alder coupling reaction.

[0029] Curing of these formulations may include heating at a first temperature to promote radical initiation followed by heating at a second temperature to promote the curing of the benzoxazine. The first temperature may comprise a range from 40° C. to 150° C. The second temperature may comprise a range from 150° C. to about 300° C. Alternatively, if no radical initiator is present, the formulation is heated at a first temperature to promote benzoxazine polymerization followed by heating at an even higher temperature to promote acetylene polymerization. This may take place in the absence of a radical initiator at a temperature that is sufficiently higher. In this case, the first temperature may comprise a range from about 150° C. to 250° C. and the second temperature is higher than 250° C. The particle loading may comprise a range from 1 wt % to 60 wt %. For ceramic applications, higher content (40 wt %-60 wt %) increases the ceramic yield and reduces the voids.

[0030] In one embodiment, the formulations with acetylene-benzoxazine-SiC particles in a benzoxazine resin may create an object comprising the cured formulation. The object may have any shape and size. The object may be fabricated by injection molding followed by curing of the acetylene-benzoxazine-SiC particles in a benzoxazine resin. Fully cured structures can be achieved in minutes to hours. A higher curing temperature may decrease the curing time.

[0031] The object may also be fabricated by 3D printing using extrusion of the acetylene-benzoxazine-SiC particles in a benzoxazine resin formulation. The same extrusion process can be applied to formulations comprising the acetylene-benzoxazine-SiC particles dispersed in other curable benzoxazines, including vinyl, propargyl, and furan-functionalized benzoxazines. Other benzoxazines can be used for fabrication of extrudable formulations with acetylene-benzoxazine-SiC particles. In this case, it may be advantageous to have the formulation behave as a solid at the ambient temperature and as a liquid or a high viscosity paste at a higher temperature, such as 70° C. to 150° C. This facilitates extrusion through nozzles and to print an object that maintains shape upon printing, prior to curing. Curing in this case may take place by slowly heating the printed 3D object at temperature close to its melting temperature, for a longer time for partial curing, followed by cure completion at a higher temperature.

[0032] The object may also be fabricated by 3D printing through indirect powder bed sintering or direct powder bed sintering. In the indirect method, laser heats and cures the powder of resin formulation as mentioned before at 200° C.-300° C. range to form the structure by curing. Then the cured structure may be pyrolyzed to ceramic. In the direct method, the laser heats and pyrolyzes the resin at 700° C.-2500° C. to directly pyrolyze the matrix or pyrolyze and melt the matrix.

[0033] In another embodiment a ceramic object is fabricated. The process involved pyrolysis of the object fabricated with cured acetylene-benzoxazine-SiC particles in a benzoxazine resin. Pyrolysis is performed at a temperature comprising a range from 700° C. to 1000° C., under inert gas. The temperature is raised typically at a rate of 1-2°/min to limit shrinkage. Suitable inert gases include argon, nitrogen and the like. The crystallization of the ceramic precursor is performed by heating at a second temperature, higher than the pyrolyzing temperature, typically comprising a range from 1400° C. to 2200° C., but it may be as high as 3000° C. During crystallization process, the temperature is raised typically at a rate of 6-10° C./min.

[0034] In another embodiment, a ceramic matrix composite such as disclosed in U.S. Patent Application No. 63/170,454, is fabricated by pyrolyzing a carbon fiber reinforced polymer composites fabricated with a resin comprising the acetylene-benzoxazine-SiC particles in a benzoxazine resin, wherein the benzoxazine resin comprises a polymerizable group selected from acetylene, furan, propargyl and vinyl.

[0035] All features disclosed in the specification, including the claims, abstract, and drawings, and all the steps in any method or process disclosed, may be combined in any combination, except combinations where at least some of such features and/or steps are mutually exclusive. Each feature disclosed in the specification, including the claims, abstract, and drawings, can be replaced by alternative features serving the same, equivalent, or similar purpose, unless expressly stated otherwise.

[0036] It will be appreciated that variants of the above-disclosed and other features and functions, or alternatives thereof, may be combined into many other different systems or applications. Various presently unforeseen or unanticipated alternatives, modifications, variations, or improvements therein may be subsequently made by those skilled in the art which are also intended to be encompassed by the following claims.