PROCESS FOR PRODUCING PRE-IMPREGNATED FIBROUS MATERIAL OF THERMOPLASTIC POLYMER IN THE FORM OF DRY P

专利摘要:
The invention relates to a method for manufacturing a preimpregnated fibrous material comprising a fibrous material made of continuous fibers and at least one thermoplastic polymer matrix, characterized in that said preimpregnated fibrous material is produced in a single unidirectional ribbon or in a plurality unidirectional parallel ribbons and in that said method comprises a step of impregnation, in particular at the core, of said fibrous material in the form of a wick or of several parallel locks by said thermoplastic polymer in the form of a powder, said impregnation step being carried out with said at least one thermoplastic polymer and said fibrous material whose D90 / D10 ratio by volume of the thermoplastic polymer particles is from 1.5 to 50, in particular from 2 to 10 and the diameter ratio volume (D50) of the thermoplastic polymer particles over the average diameter of the unit fibers of said fibrous material is from 3 to 40, except for an aqueous suspension impregnation process of a fibrous material made of carbon fibers by a thermoplastic polymer and to the exclusion of any electrostatic process voluntary charge.
公开号:FR3061069A1
申请号:FR1663209
申请日:2016-12-22
公开日:2018-06-29
发明作者:Gilles Hochstetter；Pierre Babeau Arthur；Thibaut SAVART；Vincent Tanguy Francois；Denis Huze；Mathieu Capelot；Patrice Gaillard
申请人:Arkema France SA；
IPC主号:

专利说明:

Agent (s):
ARKEMA FRANCE Public limited company.
FR 3 061 069 - A1 © PROCESS FOR THE MANUFACTURE OF A FIBROUS MATERIAL PRE-IMPREGNATED WITH THERMOPLASTIC POLYMER IN THE FORM OF DRY POWDER.
(57) The invention relates to a method for manufacturing a prepreg fibrous material comprising a fibrous material made of continuous fibers and at least one thermoplastic polymer matrix, characterized in that said prepreg fibrous material is produced in a single unidirectional ribbon or in a plurality of parallel unidirectional ribbons and in that said method comprises a step of impregnation, in particular at the core, of said fibrous material which is in the form of a wick or of several parallel wicks with said thermoplastic polymer which is in the form of powder, said impregnation step being carried out with said at least one thermoplastic polymer and said fibrous material whose ratio D90 / D10 by volume of the particles of thermoplastic polymer is from 1.5 to 50, in particular from 2 to 10 and the ratio of the volume average diameter (D50) of the thermoplastic polymer particles to the average diameter unit fibers of said fibrous material is from 3 to 40, excluding an aqueous suspension impregnation process of a fibrous material consisting of carbon fibers with a thermoplastic polymer and excluding any electrostatic process in voluntary charge.
PROCESS FOR THE MANUFACTURE OF A FIBROUS MATERIAL PRE-IMPREGNATED WITH THERMOPLASTIC POLYMER IN THE FORM OF DRY POWDER [Field of the invention]
The present invention relates to a method for manufacturing a fibrous material pre-impregnated with thermoplastic polymer in the form of dry powder.
More particularly, the invention relates to a process for manufacturing a prepreg fibrous material comprising an impregnation step for the preparation of a prepreg fibrous material, in particular at heart, of reduced and controlled porosity, in view of obtaining ribbons of prepreg fibrous material, of calibrated dimensions, directly usable for the manufacture of three-dimensional composite parts.
In the present description, the term "fibrous material" means an assembly of reinforcing fibers. Before it is shaped, it is in the form of wicks. After its shaping, it comes in the form of strips (or tape), or sheets. When the reinforcing fibers are continuous, their assembly constitutes a fabric or a nonwoven (NCF). When the fibers are short, their assembly constitutes a felt or a nonwoven.
Such prepreg fibrous materials are especially intended for the production of light composite materials for the manufacture of mechanical parts having a three-dimensional structure and having good mechanical and thermal properties. When the fibers are made of carbon or the resin is loaded with suitable additives, these fibrous materials are capable of removing electrostatic charges. They therefore have properties compatible with the manufacture of parts in particular in the fields of mechanics, civil or military aeronautics, and nautical, automotive, oil and gas, in particular offshore, storage of gas, energy, health and medical, military and armaments, sports and leisure, and electronics.
Such prepreg fibrous materials are also called composite materials. They include the fibrous material, consisting of the reinforcing fibers, and a matrix constituted by the impregnation polymer. The primary role of this matrix is to maintain the reinforcing fibers in a compact form and to give the desired shape to the final product. This matrix also ensures the transfer of charge between the fibers and therefore, conditions the mechanical strength of the composite. Such a matrix also serves to protect the reinforcing fibers from abrasion and an aggressive environment, to control the surface appearance and to disperse any charges between the fibers. The role of this matrix is important for the long-term resistance of the composite material, in particular with regard to fatigue and creep.
[Prior art
Good quality of the three-dimensional composite parts made from pre-impregnated fibrous materials notably involves mastering the process of impregnating the reinforcing fibers with the thermoplastic polymer.
In the present description, the term "strip" is used to denote strips of fibrous material whose width is greater than or equal to 400mm. We use the term "ribbon" to designate ribbons of calibrated width and less than or equal to 400mm.
The term "wick" is also used to refer to the fibrous material. Hitherto, the manufacture of strips of fibrous materials reinforced by impregnation of thermoplastic polymer or thermosetting polymer has been carried out according to several methods which depend in particular on the nature of the polymer, the type of final composite material desired and its field of activity. applications. Powder deposition or angle head impregnation impregnation technologies are often used to impregnate the reinforcing fibers with thermosetting polymers, such as epoxy resins, as described in patent WO2012 / 066241A2 . These technologies are generally not directly applicable to impregnation with thermoplastic polymers, in particular those with a high glass transition temperature which have too high a viscosity in the molten state to obtain satisfactory impregnation of the fibers and semi-finished products. or good quality finishes.
Another known method of impregnation is the continuous passage of the fibers in an aqueous dispersion of polymer powder or aqueous dispersion of polymer particles or aqueous emulsion or suspension of polymer. One can for example refer to document EP0324680. In this process, a dispersion of powders of micrometric size (approximately 20 μm) is used. After soaking in the aqueous solution, the fibers are impregnated with the polymer powder. The process then involves a drying step consisting in passing the impregnated fibers through a first oven in order to evaporate the water absorbed during the soaking. A heat treatment step, consisting in passing the impregnated and dried fibers through a second heating zone, at high temperature, is then necessary to melt the polymer so that it adheres, distributes and covers the fibers.
The main drawback of this method is the homogeneity of the deposit which is sometimes imperfect. Another problem linked to this process is the drying time and the energy consumption which strongly affects the production cost. In addition, the granulometry of the powders commonly used is fine (typically 20 μm of D50 by volume) and this also increases the final cost of the pre-impregnated ribbon or sheet.
Furthermore, the drying step of this method induces porosity in the fibers pre-impregnated by evaporation of the water.
The pre-impregnated fibrous material then needs to be shaped in the form of ribbons for example.
Companies market strips of fibrous materials obtained by a method of impregnating unidirectional fibers by passing the fibers continuously through a molten bath of thermoplastic polymer containing an organic solvent such as benzophenone. One can for example refer to document US 4,541,884 from Imperial Chemical Industries. The presence of the organic solvent makes it possible in particular to adapt the viscosity of the molten mixture and to ensure good coating of the fibers. The fibers thus pre-impregnated are then shaped. They can for example be cut into strips of different widths and then placed under a press, then heated to a temperature above the melting temperature of the polymer to ensure the cohesion of the material and in particular the adhesion of the polymer to the fibers. This method of impregnation and shaping makes it possible to produce structural parts with high mechanical strength.
One of the drawbacks of this technique lies in the heating temperature required to obtain these materials. The melting point of polymers depends in particular on their chemical nature. It can be relatively high for polymers of poly (methyl methacrylate) (PMMA) type, or even very high for polymers of poly (phenylene sulfide) (PPS), poly (ether ether ketone) (PEEK) or poly ( ether ketone ketone) (PEKK) for example. The heating temperature can therefore rise to temperatures above 250 ° C, and even above 350 ° C, temperatures which are much higher than the boiling point and the flash point of the solvent, which are respectively 305 ° C and 150 ° C for benzophenone. In this case, there is an abrupt departure of the solvent, inducing a high porosity within the fibers and consequently causing the appearance of defects in the composite material. The process is therefore difficult to reproduce and involves risks of explosion endangering operators. Finally, the use of organic solvents should be avoided for environmental reasons and the health and safety of operators.
The document EP 0 406 067, filed in the joint names of Atochem and the French State, as well as the document 2010 201 367 describe a technique for impregnation on a fluidized bed of polymer powder. The fibers enter a closed fluidization tank where, as regards EP 0 406 067, they are optionally separated from each other by means of rollers or grooved rolls, the fibers being electrostatically charged, by friction in contact with these rollers or cylinders. This electrostatic charge allows the polymer powder to stick to the surface of the fibers and thus to impregnate them.
International application WO 2016/062896 describes a wicking of wick by an electrostatic process under voluntary charge, by grounding of the wick and application of a potential difference between the tip of a spray gun or nozzles and the wick .
The document WO2008 / 135663 describes, in a third variant, the production of an impregnated fiber ribbon. In this document, the fiber ribbon is already preformed prior to the impregnation step, in the form of a ribbon formed of fibers held together by restraining means. The ribbon thus preformed is previously charged with static electricity and immersed in an enclosure containing a fluidized bed of fine particles of polymer suspended in the compressed air, so as to coat the ribbon with a layer of polymer coating. Such a document does not allow impregnation of one or more wicks of fibers simultaneously nor a continuous shaping of the prepreg wicks in the form of ribbons.
Document EP2586585 also describes the principle of impregnating fibers by passing them through a fluidized bed of polymer particles. However, it does not describe a continuous shaping of one or more wicks thus impregnated, in the form of one or more parallel unidirectional ribbons.
Application US 2002/0197397 describes a process for impregnating fibers with a mixture of polymer powders, said mixing being carried out without prior compounding directly in a fluidized bed.
International application WO 2015/121583 describes a process for manufacturing a fibrous material pre-impregnated by impregnating said material in a fluidized bed then hot calendering of said wick.
Hot calendering is carried out downstream of the impregnation device and makes it possible to homogenize the distribution of the polymer and the impregnation of the fibers. The porosity obtained is controlled and reproducible but not quantified.
The document EP0335186 describes the possibility of using a calender or a press to compact a composite comprising prepreg metal fibers, used for the manufacture of molded bodies for shielding against electromagnetic radiation. It does not describe the fact of impregnating one or more wicks of fibers and of shaping them, continuously, in the form of one or more parallel unidirectional tapes by hot calendering.
Regarding the shaping of pre-impregnated fibrous materials in the form of calibrated ribbons, suitable for the production of three-dimensional composite parts by automatic removal by means of a robot, this is generally carried out in post-processing.
Thus, the document WO92 / 20521 describes the possibility of impregnating a wick of fibers by passing it through a fluidized bed of particles of thermoplastic powder. The fibers thus covered with polymer particles are heated in an oven or a heating device so that the polymer penetrates well and covers the fibers. A post-treatment of the pre-impregnated fibrous reinforcement obtained can consist in passing it through a set of polishing roller making it possible to improve the impregnation by the still liquid matrix. One or more superimposed fibrous reinforcements can also be placed between two rollers so as to form a strip. Such a document does not make it possible to impregnate one or more wicks of fibers and to form, continuously, the wicks prepreg in the form of one or more parallel unidirectional tapes.
The quality of the ribbons of prepreg fibrous material, and therefore the quality of the final composite material, depends not only on the homogeneity of the impregnation of the fibers and therefore on the control and reproducibility of the porosity of the prepreg fibrous material. , but also the size and more particularly the width and thickness of the final ribbons. Regularity and control of these two dimensional parameters indeed improve the mechanical strength of the materials.
Currently, whatever the method used for the impregnation of fibrous materials, the manufacture of ribbons of small width, that is to say of width less than 400mm, generally requires a slitting (i.e. cutting) of strips of width greater than 400 mm, also called tablecloths. The ribbons thus dimensioned are then taken up to be deposited by a robot using a head. In addition, the rolls of plies not exceeding a length of the order of 1 km, the ribbons obtained after cutting are generally not long enough to manufacture certain large composite parts during removal by robot. The ribbons must therefore be cut back to obtain a greater length, thus creating extra thicknesses. These extra thicknesses lead to the appearance of heterogeneities which are detrimental to the obtaining of good quality composite materials constituting said composite parts.
In addition, these extra thicknesses require a machine stop and restart of the robot and therefore loss of time and productivity.
Current techniques for impregnating fibrous materials and shaping such fibrous materials pre-impregnated in the form of calibrated tapes therefore have several drawbacks. It is for example difficult to homogeneously heat a molten mixture of thermoplastic polymers in a die and at the outlet of the die, to the core of the material, which deteriorates the quality of the impregnation. In addition, the difference in temperature between the fibers and a molten mixture of polymers at the level of the impregnation process also affects the quality and the homogeneity of the impregnation. In addition, this method of impregnation by melt does not make it possible to obtain high levels of fibers or high production speeds because of the high viscosity of the thermoplastic resins, in particular when they have high glass transition temperatures, which is necessary to obtain high performance composite materials. The use of organic solvents generally involves the appearance of defects in the material as well as environmental, health and safety risks in general. The shaping, by post-treatment at high temperature of the fibrous material pre-impregnated in the form of strips, remains difficult because it does not always allow a homogeneous distribution of the polymer within the fibers which results in obtaining a material of lower quality, with poorly controlled porosity. The slitting of plies to obtain calibrated ribbons and the splicing of these ribbons induces an additional manufacturing cost. The ripping also generates significant dust problems which pollute the ribbons of prepreg fibrous materials used for robot removal and can cause robot malfunctions and / or imperfections on the composites. This potentially results in robot repair costs, production stoppage and the disposal of non-compliant products. Finally, during the slitting step, a non-negligible quantity of fibers is deteriorated, inducing a loss of properties, and in particular a reduction in the mechanical resistance and in the conductivity, of the ribbons of prepreg fibrous material.
Furthermore, the impregnation is not always carried out to the core and if the said documents cited above indicate an impregnation to the core, it turns out that the porosity obtained is too great, in particular for the applications listed above.
[Technical problem
The invention therefore aims to remedy at least one of the drawbacks of the prior art. The invention aims in particular to propose a method for manufacturing a prepreg fibrous material, by an impregnation technique associating a control of the residence time in the impregnation device with a control of the development of said fibrous material at level of said device, and to obtain a prepreg fibrous material having an impregnation of the fibers, in particular at the core, and of controlled dimensions, with a reduced, controlled and reproducible porosity on which the performance of the final composite part depends.
[Brief description of the inventionl
To this end, the subject of the invention is a method of manufacturing a prepreg fibrous material comprising a fibrous material made of continuous fibers and at least one thermoplastic polymer matrix, comprising a step of impregnating, in particular at the core, of said material. fibrous in the form of a wick or of several parallel wicks by at least one thermoplastic polymer matrix in the form of a powder.
The invention also relates to a unidirectional ribbon of prepreg fibrous material, in particular ribbon wound on a reel, characterized in that it is obtained by a process as defined above.
The invention further relates to a use of the ribbon as defined above in the manufacture of three-dimensional parts. Said manufacture of said composite parts relates to the fields of transport, in particular automobile, oil and gas, in particular offshore, gas storage, civil or military aeronautics, nautical, rail; renewable energies, in particular wind, tidal, energy storage devices, solar panels; thermal protection panels; sports and leisure, health and medical, ballistics with parts for weapons or missiles, security and electronics.
The invention also relates to a three-dimensional composite part, characterized in that it results from the use of at least one unidirectional ribbon of pre-impregnated fibrous material as defined above.
[Detailed description of the inventionl
The subject of the invention is a method of manufacturing a prepreg fibrous material comprising a fibrous material made of continuous fibers and at least one thermoplastic polymer matrix, characterized in that said prepreg fibrous material is produced in a single unidirectional ribbon or in a plurality of unidirectional parallel ribbons and in that said method comprises a step of impregnation, in particular at the core, of said fibrous material which is in the form of a wick or of several parallel wicks with said thermoplastic polymer which is in the form of powder, said impregnation step being carried out with said at least one thermoplastic polymer and said fibrous material whose ratio D90 / D10 by volume of the particles of thermoplastic polymer is comprised from 1.5 to 50, in particular from 2 to 10 and the ratio of diameter volume average (D50) of the thermoplastic polymer particles over the diameter re means of the unitary fibers of said fibrous material is from 3 to 40, excluding a process of impregnation in aqueous suspension of a fibrous material consisting of carbon fibers with a thermoplastic polymer, and excluding any electrostatic process under voluntary charge.
The inventors unexpectedly found that, on the one hand, the control of the residence time in the powder made it possible to impregnate the fibrous material with the thermoplastic polymer matrix, in particular at heart with a well-controlled powder (resin) content and d 'other hand that below a D50 of 25pm, the particle size is too small to be fluidized or correctly projected in particular by spray gun (s) or nozzle (s) at the inlet of the roller, which leads to a poor implementation and therefore poor impregnation.
Polymer matrix
The term “thermoplastic” or “thermoplastic polymer” is understood to mean a material which is generally solid at room temperature, which can be semi-crystalline or amorphous, and which softens during an increase in temperature, in particular after its glass transition temperature (Tg) has passed. and flows at a higher temperature when it is amorphous, or which may exhibit a frank melting on passing its so-called melting temperature (Tf) when it is semi-crystalline, and which becomes solid again when the temperature decreases below its crystallization temperature (for a semi-crystalline) and below its glass transition temperature (for an amorphous).
The Tg and the Tf are determined by differential scanning calorimetry (DSC) according to the standard 11357-2: 2013 and 11357-3: 2013 respectively.
As regards the polymer constituting the impregnation matrix of the fibrous material, it is advantageously a thermoplastic polymer or a mixture of thermoplastic polymers. This polymer or mixture of thermoplastic polymers is ground in powder form, so that it can be used in a device such as a tank, in particular in a fluidized bed.
The device in the form of a tank, in particular in a fluidized bed can be opened or closed.
Optionally, the thermoplastic polymer or mixture of thermoplastic polymers further comprises carbonaceous fillers, in particular carbon black or carbonaceous nanofillers, preferably chosen from carbonaceous nanofillers, in particular graphenes and / or carbon nanotubes and / or carbon nanofibrils or their mixtures. These charges ίο conduct electricity and heat, and therefore improve the lubrication of the polymer matrix when it is heated.
Optionally, said thermoplastic polymer comprises at least one additive, in particular chosen from a catalyst, an antioxidant, a thermal stabilizer, a UV stabilizer, a light stabilizer, a lubricant, a filler, a plasticizer, a flame retardant, a nucleating agent , a chain extender and a dye or a mixture thereof.
According to another variant, the thermoplastic polymer or mixture of thermoplastic polymers can also comprise liquid crystal polymers or cyclized poly (butylene terephthalate), or mixtures containing them, such as the CBT100 resin sold by the company CYCLICS CORPORATION. These compounds make it possible in particular to fluidify the polymer matrix in the molten state, for better penetration into the core of the fibers. Depending on the nature of the polymer, or mixture of thermoplastic polymers, used to produce the impregnation matrix, in particular its melting point, one or the other of these compounds will be chosen.
The thermoplastic polymers forming part of the impregnation matrix of the fibrous material can be chosen from:
- polymers and copolymers of the family of aliphatic, cycloaliphatic polyamides (PA) or semi-aromatic PAs (also called polyphthalamides (PPA)),
- polyureas, in particular aromatics,
- polymers and copolymers of the acrylic family such as polyacrylates, and more particularly polymethyl methacrylate (PMMA) or its derivatives
- polymers and copolymers of the polyarylether ketone family (PAEK) such as poly (ether ether ketone) (PEEK), or polyarylether ketone ketones (PAEKK) such as poly (ketone ether ketone) (PEKK) or their derivatives,
- aromatic polyether imides (PEI),
- polyarylsulfides, in particular polyphenylene sulfides (PPS),
- polyarylsulfones, in particular polyphenylene sulfones (PPSU), polyolefins, in particular polypropylene (PP);
- polylactic acid (PLA),
- polyvinyl alcohol (PVA),
- fluorinated polymers, in particular poly (vinylidene fluoride) (PVDF), or polytetrafluoroethylene (PTFE) or polychlorotrifluoroethylene (PCTFE), and mixtures thereof.
Advantageously, when said thermoplastic polymer is in a mixture, it is added to the tank in the form of powder obtained beforehand by “dry blend” or compound or directly in the tank in the form of “dry blend”.
Advantageously, it is added in the form of powder obtained beforehand by “dry blend” or directly in the tank in the form of “dry blend” and the mixture is a mixture of PEKK and PEI.
Advantageously, when said polymer is a mixture of two polymers P1 and P2, the proportion by weight of polymer P1 and P2 is between 1-99% to 99-1%.
Advantageously, the PEKK / PEI mixture is comprised from 90-10% to 60-40% by weight, in particular from 90-10% to 70-30% by weight.
The thermoplastic polymer may correspond to the final non-reactive polymer which will impregnate the fibrous material or to a reactive prepolymer, which will also impregnate the fibrous material, but is capable of reacting on itself or with another prepolymer, depending on the end of chain carried. by said prepolymer, after impregnation, or even with a chain extender and in particular during heating at the level of a heating calender.
According to a first possibility, said prepolymer can comprise or consist of, at least one reactive prepolymer (polyamide) carrying on the same chain (that is to say on the same prepolymer), of two terminal functions X 'and Y' respectively coreactive functions between them by condensation, more particularly with X 'and Y' being amine and carboxy or carboxy and amine respectively. According to a second possibility, said prepolymer can comprise or consist of, at least two polyamide prepolymers reactive with each other and each carrying two terminal functions X ′ or Y ′, identical (identical for the same prepolymer and different between the two prepolymers), said function X 'of a prepolymer being able to react only with said function Y' of the other prepolymer, in particular by condensation, more particularly with X 'and Y' being amine and carboxy or carboxy and amine respectively.
According to a third possibility, said prepolymer can comprise or consist of, at least one prepolymer of said thermoplastic polyamide polymer, carrying n terminal reactive functions X, chosen from: -NH2, -CO2H and -OH, preferably NH2 and -CO2H with n being 1 to 3, preferably 1 to 2, more preferably 1 or 2, more particularly 2 and at least one chain extender Y-A'-Y, with A 'being a hydrocarbon biradical, of non-polymeric structure, carrying of 2 identical terminal reactive functions Y, reactive by polyaddition with at least one function X of said prepolymer a1), preferably of molecular mass less than 500, more preferably less than 400.
The number average molecular weight Mn of said final polymer of the thermoplastic matrix is preferably in a range from 10,000 to 40,000, preferably from 12,000 to 30,000. These Mn values can correspond to inherent viscosities greater than or equal to 0.8 such as determined in m-cresol according to ISO standard 307: 2007 but by changing the solvent (use of m-cresol instead of sulfuric acid and the temperature being 20 ° C).
Said reactive prepolymers according to the two options mentioned above have a number average molecular weight Mn ranging from 500 to 10,000, preferably from 1000 to 6000, in particular from 2500 to 6000.
The Mn are determined in particular by calculation from the rate of the terminal functions determined by potentiometric titration in solution and the functionality of said prepolymers. The Mn masses can also be determined by size exclusion chromatography or by NMR.
The nomenclature used to define polyamides is described in standard ISO 1874-1: 2011 Plastics - Polyamide materials (PA) for molding and extrusion - Part 1: Designation, in particular on page 3 (tables 1 and 2) and is well known by the skilled person.
The polyamide can be a homopolyamide or a copolyamide or a mixture of these.
Advantageously, the polymers constituting the matrix are chosen from Polyamides (PA), in particular chosen from aliphatic polyamides, in particular PA11 and PA12, cycloaliphatic polyamides, and semi-aromatic polyamides (polyphthalamides) optionally modified by urea units, and their copolymers, Polymethyl methacrylate (PPMA) and its copolymers, Polyether imides (PEI), Poly (phenylene sulfide) (PPS),
Poly (phenylene sulfone) (PPSU), Polyetherketoneketone (PEKK),
Polyetheretherketone (PEEK), fluorinated polymers such as poly (vinylidene fluoride) (PVDF).
For fluorinated polymers, a homopolymer of vinylidene fluoride (VDF of formula CH2 = CF2) or a copolymer of VDF comprising by weight at least 50% by mass of VDF and at least one other monomer copolymerizable with VDF can be used. The VDF content must be greater than 80% by mass, or better still 90% by mass, to ensure good mechanical resistance to the structural part, especially when it is subjected to thermal and chemical stresses. The comonomer can be a fluorinated monomer such as for example vinyl fluoride.
PAEK (PolyArylEtherKetone) such as polyether ketones PEK, poly (ether ether ketone) PEEK, poly (ether ketone) are advantageously used for structural parts which must withstand high temperatures, in addition to fluorinated polymers. ketone) PEKK, Poly (ketone ether ketone ketone ether) PEKEKK or PAs with a high glass transition temperature Tg). Advantageously, said thermoplastic polymer is selected from amorphous polymers whose glass transition temperature is such that Tg> 80 ° C and / or from semi-crystalline polymers whose melting temperature Tf is> 150 ° C.
Advantageously, said thermoplastic polymer is:
- an aliphatic polyamide chosen from polyamide 6 (PA-6), polyamide 11 (PA-11), polyamide 12 (PA-12), polyamide 66 (PA-66), polyamide 46 (PA-46) , polyamide 610 (PA-610), polyamide 612 (PA-612), polyamide 1010 (PA-1010), polyamide 1012 (PA-1012), or a mixture thereof or a copolyamide thereof this,
a semi-aromatic polyamide, optionally modified by urea units, in particular a semi-aromatic polyamide of formula X / YAr, as described in EP1505099, in particular a semi-aromatic polyamide of formula A / XT in which A is chosen from a motif obtained from an amino acid, a motif obtained from a lactam and a motif corresponding to the formula (diamine in Ca). (diacid in Cb), with a representing the number of carbon atoms in the diamine and b representing the number of carbon atoms of the diacid, a and b each being between 4 and 36, advantageously between 9 and 18, the motif (diamine in Ca) being chosen from aliphatic diamines, linear or branched, diamines cycloaliphatic and alkylaromatic diamines and the unit (Cb diacid) being chosen from aliphatic diacids, linear or branched, cycloaliphatic diacids and aromatic diacids .;
XT denotes a motif obtained from the polycondensation of a Cx diamine and terephthalic acid, with x representing the number of carbon atoms of the Cx diamine, x being between 6 and 36, advantageously between 9 and 18, in particular a polyamide of formula A / 6T, A / 9T, A / 10T or A / 11T, A being as defined above, in particular a polyamide PA6 / 6T, 66 / 6T, 6I / 6T, MPMDT / 6T, PA11 / 10T, 11 / 6T / 10T, MXDT / 10T or MPMDT / 10T, BACT / 10T, MXD6 and MXD10 and block copolymers, especially polyamide / polyether (PEBA).
T corresponds to terephthalic acid, MXD corresponds to m-xylylene diamine, MPMD corresponds to methylpentamethylene diamine and BAC corresponds to bis (am inomethyl) cyclohexane.
Fibrous material:
Regarding the fibers of which said fibrous material is made, these are in particular fibers of mineral, organic or vegetable origin. Among the fibers of mineral origin, mention may be made of carbon fibers, glass fibers, basalt fibers, silica fibers, or silicon carbide fibers for example. Among the fibers of organic origin, mention may be made of fibers based on a thermoplastic or thermosetting polymer, such as semi-aromatic polyamide fibers, aramid fibers or polyolefin fibers for example. Preferably, they are based on amorphous thermoplastic polymer and have a glass transition temperature Tg greater than the Tg of the polymer or mixture of thermoplastic polymer constituting the impregnation matrix when the latter is amorphous, or greater than the Tf of the polymer or mixture of thermoplastic polymer constituting the impregnation matrix when the latter is semi-crystalline. Advantageously, they are based on semi-crystalline thermoplastic polymer and have a melting temperature Tf greater than the Tg of the polymer or mixture of thermoplastic polymer constituting the impregnation matrix when the latter is amorphous, or greater than the Tf of the polymer or mixture of thermoplastic polymer constituting the impregnation matrix when the latter is semi-crystalline. Thus, there is no risk of fusion for the organic fibers constituting the fibrous material during the impregnation by the thermoplastic matrix of the final composite. Among the fibers of vegetable origin, mention may be made of natural fibers based on flax, hemp, lignin, bamboo, notably spider silk, sisal, and other cellulosic fibers, in particular viscose. These fibers of plant origin can be used pure, treated or coated with a coating layer, in order to facilitate the adhesion and the impregnation of the matrix of thermoplastic polymer. The fibrous material can also be a fabric, braided or woven with fibers.
It can also correspond to fibers with retaining threads.
These fibers of constitution can be used alone or in mixtures. Thus, organic fibers can be mixed with the mineral fibers to be impregnated with thermoplastic polymer and form the pre-impregnated fibrous material.
The strands of organic fibers can have several grammages. They can also have several geometries. The fibers may be in the form of short fibers, which then make up the felts or nonwovens which may be in the form of strips, sheets, or pieces, or in the form of continuous fibers, which make up the 2D fabrics, the braids or unidirectional (UD) or non-woven fibers. The fibers constituting the fibrous material can also be in the form of a mixture of these reinforcing fibers of different geometries. Preferably, the fibers are continuous.
Preferably, the fibrous material consists of continuous fibers of carbon, glass or silicon carbide or a mixture thereof, in particular carbon fibers. It is used in the form of a wick or several wicks.
Advantageously, said fibrous material consists of glass fibers and said ratio D50 / average diameter of the unit fibers is from 3 to 15, in particular from 3 to 10.
In particular, said fibrous material consists of glass fibers and said ratio D50 / average diameter of the unit fibers is from 4 to 15, in particular from 4 to
10.
Advantageously, said fibrous material consists of carbon fibers and said ratio D50 / average diameter of the unit fibers is comprised from 10 to 40.
In prepreg materials also called "ready to use", the polymer or mixture of thermoplastic impregnation polymers is distributed uniformly and homogeneously around the fibers. In this type of material, the thermoplastic impregnation polymer must be distributed as homogeneously as possible within the fibers in order to obtain a minimum of porosities, that is to say a minimum of voids between the fibers. Indeed, the presence of porosities in this type of material can act as stress concentration points, during a mechanical tensile stress for example, and which then form points of initiation of rupture of the pre-fibrous material. -impregnated and weaken it mechanically. A homogeneous distribution of the polymer or mixture of polymers therefore improves the mechanical strength and the homogeneity of the composite material formed from these pre-impregnated fibrous materials.
Thus, in the case of so-called “ready-to-use” prepreg materials, the fiber content in said impregnated fibrous material is from 45 to 65% by volume, preferably from 50 to 60% by volume, in particular of 54 to 60% by volume.
The measurement of the impregnation rate can be carried out by image analysis (use of a microscope or of a digital camera or camera, in particular), of a cross section of the ribbon, by dividing the surface of the ribbon impregnated by the polymer. by the total surface of the product (impregnated surface plus porosity surface). In order to obtain a good quality image it is preferable to coat the cut ribbon in its transverse direction in a standard polishing resin and to polish with a standard protocol allowing the observation of the sample under the microscope magnification at least 6 times .
Advantageously, the porosity rate of said prepreg fibrous material is between 0% and 30%, in particular from 1% to 10%, in particular from 1% to 5%.
The porosity rate corresponds to the closed porosity rate and can be determined either by electron microscopy or as the relative difference between the theoretical density and the experimental density of said pre-impregnated fibrous material as described in the examples part of the present invention.
Impregnation step:
Said impregnation step is carried out by powder deposition, fluidized bed or by spraying using spray gun (s) or powder nozzle (s) at the inlet of the roller. Advantageously, it is carried out by a fluidized bed in an impregnation tank. An example of a unit for implementing the fluidized bed manufacturing process in an impregnation tank is described in international application WO 2015/121583 and is shown in FIG. 1, with the exception of the tank (otherwise called tank d 'impregnation which in the case of the invention comprises a fluidized bed provided with a tying piece (Figure 3) which can be a compression roller (Figure
4)) ·
The step of impregnating the fibrous material is carried out by passing one or more wicks through a continuous impregnation device, comprising a tank (20), comprising in particular a fluidized bed (22) of polymer powder.
The polymer powder (s) or polymer is suspended in a gas G (air for example) introduced into the tank and circulating in the tank through a hopper 21. The wick (s) are circulated in this fluidized bed 22.
The tank can have any shape, in particular cylindrical or rectangular, in particular a rectangular parallelepiped or a cube, advantageously a rectangular parallelepiped.
The tank can be an open or closed tank. Advantageously, it is open. In the case where the tank is closed, it is then equipped with a sealing system so that the polymer powder cannot escape from said tank.
This impregnation step is therefore carried out dry, that is to say that the thermoplastic polymer matrix is in powder form, in particular in suspension in a gas, in particular air, but cannot be dispersed in solvent or in water.
Each wick to be impregnated is unwound from a device 10 with reels 11 under the traction generated by cylinders (not shown). Preferably, the device 10 comprises a plurality of reels 11, each reel making it possible to unwind a wick to be impregnated. Thus, it is possible to impregnate several wicks of fibers simultaneously. Each reel 11 is provided with a brake (not shown) so as to apply tension to each strand of fibers. In this case, an alignment module 12 makes it possible to arrange the strands of fibers parallel to one another. In this way the strands of fibers cannot be in contact with each other, which makes it possible to avoid mechanical degradation of the fibers by friction between them.
The wick of fibers or the wicks of parallel fibers then pass into a tank (20), comprising in particular a fluidized bed (22), provided with a tying piece which is a compression roller 23 in the case of the figure 1. The wick of fibers or the wicks of parallel fibers then comes out of the tank after impregnation after checking the residence time in the powder.
The inventors therefore unexpectedly found that controlling the residence time in the powder made it possible to impregnate the fibrous material with the thermoplastic polymer matrix, with a well-controlled resin content.
They also found that through the use of at least one fixture the impregnation was improved compared to the prior art methods, in particular, the impregnation is at heart.
By piece of equipment is meant any system on which the wick can scroll in the tank. The fixture can have any shape as long as the wick can scroll over it.
An example of a fitting piece, without restricting the invention to it, is detailed in Figure 3.
This impregnation is carried out in order to allow the polymer powder to penetrate into the heart of the wick of fiber and to adhere to the fibers sufficiently to support the transport of the powder wick out of the tank. The wick (s) pre-impregnated with the powder is (are) directed (s) then to a heating calendering device, with the possibility of preheating before calendering and possible post-calendering heating.
Optionally, this impregnation step can be supplemented by a step of covering the wick or of the prepreg wicks, just at the outlet of the powder impregnation tank (20) in a fluidized bed (22), and just before the calendering step. For this, the outlet lock of the tank (20) (fluidized bed 22) can be connected to a covering device (30) which may include a covering square head, as also described in patent EP0406067. The covering polymer may be the same or different from the polymer powder in a fluidized bed. Preferably, it is of the same nature. Such a covering not only makes it possible to complete the step of impregnating the fibers to obtain a final volume rate of polymer in the desired range and to avoid the presence on the surface of the prepreg wick, of a rate of fibers locally too important, which would interfere with the welding of the tapes during the manufacture of the composite part, in particular for obtaining so-called “ready-to-use” fibrous materials of good quality, but also for improving the performance of the composite material obtained.
The process of the invention as indicated above is carried out dry, excluding an electrostatic process under voluntary charge.
The expression "under voluntary load" means that a potential difference is applied between the fibrous material and the powder. The load is notably controlled and amplified. The grains of powder then permeate the fibrous material by attraction of the charged powder opposite the fiber. The powder can be electrically charged, negatively or positively, by different means (potential difference between two metal electrodes, mechanical friction on metal parts, etc.) and charge the fiber inversely (positively or negatively).
The process of the invention does not exclude the presence of electrostatic charges which could appear by friction of the fibrous material on the elements of the processing unit before or at the level of the tank but which are in any event of the involuntary charges.
Advantageously, the content of fibers in said impregnated fibrous material is from 45 to 65% by volume, preferably from 50 to 60% by volume, in particular from 54 to 60% by volume.
Below 45% of fibers, the reinforcement has no interest in terms of mechanical properties.
Above 65%, the process limits are reached and the mechanical properties are lost.
If the fibrous material, such as fiberglass, has a sizing, an optional step of de-sizing can be carried out before the passage of the fibrous material in the tank. The term “sizing” designates the surface treatments applied to the reinforcing fibers at the outlet of the die (textile sizing) and on the fabrics (plastic sizing).
The textile sizing applied to the filaments, at the outlet of the die consists of depositing a bonding agent ensuring the cohesion of the filaments between them, reducing abrasion and facilitating subsequent handling (weaving, draping, knitting) and avoiding the formation of charges. electrostatic.
The plastic sizing or finish applied to the fabrics consists of depositing a bridging agent whose roles are to ensure a physico-chemical bond between the fibers and the resin and to protect the fiber from its environment.
Advantageously, the fiber content in said impregnated fibrous material is between 50 and 60%, in particular from 54 to 60% by volume.
Advantageously, the residence time in the powder is from 0.01 s to 10 s, preferably from 0.1 s to 5 s, and in particular from 0.1 s to 3 s.
The residence time of the fibrous material in the powder is essential for the impregnation, in particular at the heart, of said fibrous material.
Below 0.1s, the impregnation is not good at heart.
Beyond 10 s, the rate of polymer matrix impregnating the fibrous material is too high and the mechanical properties of the prepreg fibrous material will be poor.
Advantageously, the tank used in the process of the invention comprises a fluidized bed and said impregnation step is carried out with simultaneous development of said wick or said wicks between the inlet and the outlet of said fluidized bed.
The expression "inlet of the fluidized bed" corresponds to the vertical tangent of the edge of the tank which comprises the fluidized bed.
The expression "leaving the fluidized bed" corresponds to the vertical tangent of the other edge of the tank which comprises the fluidized bed.
Depending on the geometry of the tank, the distance between the inlet and the outlet therefore corresponds to the diameter in the case of the cylinder, to the side in the case of a cube or to the width or length in the case of a rectangular parallelepiped. The blooming consists in singling out as much as possible each filament constituting said wick of the other filaments which surround it in its closest space. It corresponds to the transverse spread of the wick.
In other words, the transverse spread or the width of the wick increases between the inlet of the fluidized bed (or of the tank comprising the fluidized bed) and the outlet of the fluidized bed (or of the tank comprising the fluidized bed) and thus allows an improved impregnation, in particular at the heart of the fibrous material.
The fluidized bed can be opened or closed, in particular it is open.
Advantageously, the fluidized bed comprises at least one fitting piece, said wick or said wicks being in contact with part or all of the surface of said at least one fitting piece.
Figure 3 details a tank (20) comprising a fluidized bed (22) with a fitting piece, adjustable in height (82).
The wick (81a) corresponds to the wick before impregnation which is in contact with part or all of the surface of said at least one mooring piece and therefore runs partially or totally on the surface of the mooring piece (82 ), said system (82) being immersed in the fluidized bed where impregnation takes place. Said wick then emerges from the tank (81b) after checking the residence time in the powder.
Said wick (81a) can be in contact or not with the edge of the tank (83a) which can be a rotary or fixed roller or a parallelepiped edge.
Advantageously, said wick (81a) is in contact or not with the edge of the tank (83a).
Advantageously, the edge of the tank (83b) is a roller, in particular cylindrical and rotary.
Said wick (81b) can be in contact or not with the edge of the tank (83b) which can be a roller, in particular cylindrical and rotary or fixed, or a parallelepiped edge.
Advantageously, said wick (81b) is in contact with the edge of the tank (83b). Advantageously, the edge of the tank (83b) is a roller, in particular cylindrical and rotary.
Advantageously, said wick (81a) is in contact with the edge of the tank (83a) and the edge of the tank (83b) is a roller, in particular cylindrical and rotary, and said wick (81b) is in contact with the edge. of the tank (83b), and the edge of the tank (83b) is a roller, in particular cylindrical and rotary.
Advantageously, said fitting piece is perpendicular to the direction of said wick or said wicks.
Advantageously, said development of said wick or said wicks is carried out at least at the level of said at least one fitting piece.
The development of the wick therefore takes place mainly at the level of the fitting piece but can also be carried out at the edge or edges of the tank if there is contact between the wick and said edge.
In another embodiment, said at least one fitting piece is a compression roller of convex, concave or cylindrical shape.
The convex shape is favorable to blooming while the concave shape is unfavorable to blooming although it is done nevertheless.
The expression "compression roller" means that the scrolling wick is supported partially or completely on the surface of said compression roller, which induces the blooming of said wick.
Advantageously, said at least one compression roller is of cylindrical shape and the percentage of development of said wick or said wicks between the inlet and the outlet of said fluidized bed is from 1% to 400%, preferably between 30% and 400% preferably between 30% and 150%, preferably between 50% and 150%.
The blooming depends on the fibrous material used. For example, the flourishing of a carbon fiber material is much more important than that of a flax fiber.
Flourishing is also a function of the number of fibers or filaments in the wick, their average diameter and their cohesion by size.
The diameter of said at least one compression roller is from 3 mm to 500 mm, preferably from 10 mm to 100 mm, in particular from 20 mm to 60 mm. Below 3 mm, the deformation of the fiber induced by the compression roller is too great.
Advantageously, the compression roller is cylindrical and not grooved and in particular is metallic.
When the fitting piece is at least one compression roller, according to a first variant, only one compression roller is present in the fluidized bed and said impregnation is carried out at the angle ai formed by said wick or said wicks between the inlet of said compression roller and the vertical tangent to said compression roller.
The angle ai formed by said wick or said wicks between the inlet of said compression roller and the vertical tangent to said compression roller allows the formation of an area in which the powder will concentrate thus leading to a "wedge effect" which with the simultaneous development of the wick by said compression roller allows impregnation over a larger width of wick and therefore an improved impregnation compared to the techniques of the improved prior art. The coupling with the controlled residence time then allows impregnation to the core.
Advantageously, the angle ai is comprised from 0 to 89 °, preferably 5 ° to 85 °, preferably from 5 ° to 45 °, preferably from 5 ° to 30 °.
However, an angle ai of 0 to 5 ° is likely to generate risks of mechanical stress, which will lead to breakage of the fibers, and an angle ai of 85 ° to 89 ° does not create sufficient mechanical force to create the "corner effect".
A value of the angle equal to 0 ° therefore corresponds to a vertical fiber. It is obvious that the height of the cylindrical compression roller is adjustable, thus making it possible to position the fiber vertically.
It would not go beyond the scope of the invention if the wall of the tank was pierced so as to be able to allow the wick to exit.
Advantageously, the edge of the tank (83a) is equipped with a roller, in particular cylindrical and rotary, on which said wick or said wicks pass, thus leading to prior blooming.
Advantageously, one or more embarrassments are present downstream of the tank comprising the fluidized bed at the level of which or which the blooming is initiated.
Advantageously, the blooming is initiated at the level of said above-mentioned interruptions and continues at the level of the edge of the tank (83a).
The blooming is then maximum after passage at the level of the compression roller (s).
FIG. 4 describes an embodiment, without being limited thereto, to a single compression roller, with a tank (20) comprising a fluidized bed (22) in which a single cylindrical compression roller is present and showing the 'angle ai.
The arrows at the fiber indicate the direction of travel of the fiber. Advantageously, the level of said powder in said fluidized bed is at least located at the mid-height of said compression roller.
It is quite obvious that the “corner effect” caused by the angle promotes impregnation on one side, but the development of said wick obtained thanks to the compression roller also makes it possible to have an impregnation on the other face. of said wick. In other words, said impregnation is favored on one face of said wick or said wicks at the angle formed by said wick or said wicks between the inlet of said at least one compression roller Ri and the vertical tangent to the compression roller Ri but the blooming also allows to impregnate the other face.
The angle is as defined above.
According to a second variant, when the fitting piece is at least one compression roller, then two compression rollers Ri and R ₂ are in said fluidized bed and said impregnation is carried out at the angle ai formed by said wick or said wicks between the inlet of said compression roller Ri and the vertical tangent to said compression roller Ri and / or at the level of the angle 02 formed by said wick or said wicks between the inlet of said compression roller R2 and the vertical tangent to said compression roller R2, said compression roller Ri preceding said compression roller R2 and said wick or said wick being able to pass above (FIG. 5 and 6) or below (FIG. 7 and 8) of roller R2.
Advantageously, when the two rollers are at different heights and the wick passes over the roller R2, then 02 "is included from 0 to 90 °.
Advantageously, the two compression rollers are of identical or different shape and chosen from a convex, concave or cylindrical shape.
Advantageously, the two compression rollers are identical and non-grooved cylindrical and in particular metallic.
The diameter of the two compression rollers can also be the same or different and is as defined above.
Advantageously, the diameter of the two compression rollers is identical.
The two compression rollers Ri and R2 may be at the same level with respect to each other and with respect to the bottom of the tank (Figures 6 and 7) or offset with respect to each other and with respect to at the bottom of the tank, the height of the compression roller Ri being greater or less than that of the compression roller R2 relative to the bottom of the tank (Figures 5 and 8).
Advantageously, said impregnation is therefore carried out at the angle ai formed by said wick or said wicks between the inlet of said compression roller Ri and the vertical tangent to said compression roller on one face of said wick and at the level of l angle 02 formed by said wick or said wicks between the inlet of said compression roller R2 and the vertical tangent to said compression roller R2 on the opposite face of said wick which is obtained by passing above the roller R2.
Advantageously, said wick in this embodiment is subject to blooming at each angle ai and 02.
FIG. 6 describes an embodiment, without being limited to this, with two compression rollers Ri and R2, Ri preceding R2, with a tank (20) comprising a fluidized bed (22) in which the two compression rollers cylindrical, at the same level and side by side, are present and showing the case where said one or more wicks come out between said compression rollers Ri and R ₂ .
In this case, the angle a ₂ is equal to 0 and said one or more wicks pass over the roller R ₂ .
The arrows at the fiber indicate the direction of travel of the fiber.
Alternatively, said wick or said wicks pass (s) at the input between said compression rollers Ri and R ₂ and spring (ent) after being in contact with part or all of the surface of said compression roller R ₂ .
Advantageously, said wick or said wicks is (are) in contact at the inlet with part or all of the surface of said compression roller Ri and comes out of the compression roller R ₂ after being in contact with part or all of the surface of said compression roller R ₂ , under the roller R ₂ , the angle a ₂ being formed by said wick or said wicks between the inlet of said compression roller R ₂ and the vertical tangent to said roller compression R ₂ . In this case, the angle a2 = 90 °.
Said impregnation is therefore carried out at the angle eu formed by said wick or said wicks between the inlet of said compression roller Ri and the vertical tangent to said compression roller on a face of said wick and at the angle a ₂ formed by said wick or said wicks between the inlet of said compression roller R ₂ and the vertical tangent to said compression roller R ₂ on the same face of said wick but the blooming also makes it possible to impregnate the other face .
Advantageously, said wick in this embodiment is subject to blooming at each angle eu and a ₂ .
FIG. 7 shows an exemplary embodiment with two compression rollers Ri and R ₂ at the same level with respect to each other.
According to another embodiment of the second variant, when two compression rollers are present then the distance between the two compression rollers Ri and R ₂ is comprised from 0.15 mm to the length equivalent to the maximum dimension of the tank, preferably between 10mm and 50mm and the height difference between the two compression rollers Ri and R ₂ is from 0 to the height corresponding to the maximum height of the tank subtracted from the diameters of the two compression rollers, preferably between 0, 15mm at the height corresponding to the maximum height of the tank subtracted from the diameters of the two compression rollers, more preferably at a height difference of between 10mm and 300mm, R ₂ being the upper compression roller.
Advantageously, when two compression rollers are present and at the same level with each other, the level of said powder in said fluidized bed is at least located at the mid-height of said two compression rollers.
FIG. 8 describes an embodiment, without being limited to this, with two compression rollers Ri and R ₂ , Ri preceding R ₂ , with a tank (20) comprising a fluidized bed (22) in which two rollers cylindrical compression at different levels are present and showing the angle ai and a ₂ .
The diameter of the compression rollers Ri and R ₂ is presented as identical in FIGS. 5, 6, 7 and 8 but the diameter of each cylindrical compression roller can be different, the diameter of the compression roller Ri can be greater or less than that of the compression roller R ₂ in the range as defined above.
Advantageously, the diameter of the two compression rollers is identical.
It would not go beyond the scope of the invention if the compression roller Ri was greater than the compression roller R ₂ .
According to a third variant, when two compression rollers are present and at different levels, then at least one third compression roller R3 is also present and located between the compression rollers Ri and R ₂ in the direction of the height (FIG. 9).
Advantageously, said wick or said wicks are (are) in contact at the input with part or all of the surface of said compression roller Ri then with part or all of the surface of said compression roller R3 and comes out after having been in contact with part or all of the surface of said compression roller R ₂ .
Advantageously, said impregnation is carried out on one face of said wick or said wicks at the angle ai formed by said wick or said wicks between the inlet of said at least one compression roller Ri and the vertical tangent to the compression roller Ri as well as at the angle 03 formed by said drill bit (s) and the vertical tangent to the compression roller R3 and on the other face than at the angle a ₂ formed by said drill bit (s) and the vertical tangent to the compression roller R ₂ .
Advantageously, when two compression rollers are present at different levels and at least one third compression roller R3 is also present, then the angle a ₂ formed by said wick or said wicks between the inlet of said at least one compression roller R ₂ and the vertical tangent to said compression roller R ₂ is included from 180 ° to 45 °, in particular from 120 ° to 60 °. Advantageously, the angle 03 is comprised from 0 ° to 180 °, advantageously from 45 ° to 135 °.
FIG. 9 describes an embodiment, without being limited to this, with a tank (20) comprising a fluidized bed (22) with two compression rollers Ri and R ₂ , Ri preceding R ₂ , and a third roller compression R3 and showing the angles ai, a ₂ and 03.
The diameter of the compression rollers Ri, R ₂ and R3 is presented as identical in FIG. 9 but the diameter of each cylindrical compression roller can be different, or two compression rollers can have the same diameter and the third a different different diameter or lower, in the range as defined above.
Advantageously, the diameter of the three compression rollers is identical. Advantageously, in this third variant, a second control of the development of said wick or said wicks is carried out at the level of the compression roller R3 and a third control of the development is carried out at the level of the compression roller R3.
The residence time in this third variant is as defined above. Advantageously, in this third variant, the level of said powder in said fluidized bed is at least located at the mid-height of said compression roller R ₂ .
It would not be departing from the scope of the invention if in this third variant, said wick or said wicks is (are) in input contact with part or all of the surface of said compression roller Ri then with part or all from the surface of said compression roller R ₂ and comes out after being in contact with part or all of the surface of said compression roller R ₃ .
According to another embodiment of the present invention, the tank used in the process of the invention is devoid of a fluidized bed but comprises a spraying system by spray gun (s) or nozzle (s) at the inlet of the roll of said powder. and said impregnation step is carried out with simultaneous development of said wick or said wicks between the inlet and the outlet of the tank.
In the same way as above, the residence time in the fluidized powder bed is controlled and the tank can be provided with the same fitting parts, in particular one or more compression rollers as defined above.
Advantageously, the residence time in the tank is from 0.01 s to 10 s, preferably from 0.1 s to 5 s, and in particular from 0.1 s to 3 s.
According to an advantageous embodiment, the present invention relates to a process as defined above, characterized in that a single thermoplastic polymer matrix is used and the thermoplastic polymer powder is fluidizable.
The term "fluidizable" means that the air flow rate applied to the fluidized bed is between the minimum fluidization flow rate (Umf) and the minimum bubbling flow rate (Umf) as shown in FIG. 17.
Below the minimum fluidization flow, there is no fluidization, the particles of polymer powder fall into the bed and are no longer in suspension and the process according to the invention cannot operate.
Above the minimum bubbling rate, the powder particles fly away and the composition of the constant fluidized bed can no longer be kept constant.
Advantageously, the volume diameter D90 of the particles is between 50 and 500 μm, advantageously from 120 to 300 μm.
Advantageously, the volume diameter D10 of the particles is from 5 to 200 μm, advantageously from 35 to 100 μm.
Advantageously, the volume average diameter of the particles of thermoplastic polymer powder is from 30 to 300 μm, in particular from 50 to 200 μm, more particularly from 70 to 200 μm.
The particle volume diameters (D10, D50 and D90) are defined according to ISO 9276: 2014.
The "D50" corresponds to the mean diameter by volume, ie the value of the particle size which divides the population of particles examined exactly in two.
The “D90” corresponds to the value at 90% of the cumulative curve of the particle size distribution by volume.
The “D10” corresponds to the corresponds to the size of 10% of the volume of the particles.
According to another embodiment of the method according to the invention, a creel is present before the tank comprising a fluidized bed for controlling the tension of said wick or said wicks at the inlet of the tank comprising a fluidized bed. Optionally, in the method according to the invention, one or more embarrassments are present after the tank comprising the fluidized bed.
Shaping step
As soon as it leaves the tank (20), in particular comprising a fluidized bed (22), the pre-impregnated wick (the parallel wicks), possibly covered with a molten polymer, is (are) shaping (s) in the form of a single unidirectional ribbon or of a plurality of parallel unidirectional ribbons, by means of a continuous calendering device comprising one or more heating calenders.
Advantageously, the heating calenders of the calendering device are coupled to rapid heating means which make it possible to heat the material not only at the surface but also at the core.
The wick blooming at the outlet of the tank (20) comprising a fluidized bed (22) then shrinks under the effect of heating which contributes to inserting the molten polymer between the fibers of the wick thus allowing to reduce the porosity of said wick and favoring an impregnation, in particular at the heart of said wick.
The mechanical stress of the calenders coupled with these rapid heating means makes it possible to eliminate the presence of porosities and to distribute the polymer in a homogeneous manner, in particular when the fibrous material is a material known as "ready to use".
Advantageously, this hot calendering not only makes it possible to heat the impregnation polymer so that it penetrates, adheres and covers the fibers uniformly, but also to control the thickness and the width of the ribbon or bands of pre-fibrous material. -impregnated.
To be able to produce a plurality of parallel unidirectional tapes, that is to say as many tapes as parallel prepreg wicks, passed through the fluidized bed, the heating calenders, referenced (51), (52), (53) in the diagram of Figure 1, advantageously include a plurality of calendering grooves (73), in accordance with the number of ribbons. This number of grooves can for example go up to 200. A SYST slave system also makes it possible to regulate the pressure and / or the spacing E between the rollers (71), (75) of the calender (70), so to control the thickness ep of the ribbons. Such a grille (70) is shown schematically in Figure 2 described below.
The calendering device comprises at least one heating calender (51). Preferably, it comprises several heating calenders (51), (52), (53) mounted in parallel and / or in series with respect to the direction of travel of the wicks of fibers.
In particular, the successive calendering step is carried out gradually with pressures between the rollers which are increasing (in the direction of travel of the process) and / or a spacing between the rollers which decreases (in the direction of travel of the process) process).
Having several calenders in series makes it possible to compact the material and reduce the rate of porosities in the material and to decrease their rate. This plurality of calenders is therefore important when it is desired to produce so-called “ready-to-use” fibrous materials.
Having multiple calenders in parallel increases the number of prepreg wicks.
Advantageously, each calender of the calendering device has a heating system integrated by induction or by microwaves, preferably by microwaves, in order to heat the polymer or mixture of thermoplastic polymers. Advantageously, when the polymer or mixture of polymers comprises carbonaceous fillers, such as carbon black or carbonaceous nanofillers, preferably chosen from carbonaceous nanofillers, in particular graphenes and / or carbon nanotubes and / or carbon nanofibrils or their mixtures, the effect of heating by induction or by microwaves is amplified by the presence of these charges which then conduct heat to the heart of the material.
Advantageously, each grille (51), (52), (53) of the device is coupled to a rapid heating device (41), (42), (43), located before and / or after each grille, in order to quickly transmit thermal energy to the material and perfect the impregnation of the fibers by the molten polymer. The rapid heating device can for example be chosen from the following devices: a microwave or induction device, an infrared IR or laser device or another device allowing direct contact with the heat source such as a flame device or a hot gas. A microwave or induction device is very advantageous, in particular when it is coupled to the presence of carbon nanofillers in the polymer or mixture of polymers since the carbon nanofillers amplify the heating effect and transmit it to the heart of the material.
According to an alternative embodiment, it is also possible to combine several of these heating devices.
The method may further comprise a step of heating the wicks of the fibers, before said impregnation with, as preferred heating means, microwave heating as for the heating system of said heating calender.
Optionally, a subsequent step consists of winding the pre-impregnated and shaped tape (s). For this, the unit (100) for implementing the method comprises a winding device (60) comprising as many spools (61) as there are ribbons, a spool (61) being assigned to each ribbon. A distributor (62) is generally provided for deflecting the prepreg tapes towards their respective coils (61), while preventing the tapes from touching in order to avoid any degradation.
Figure 2 shows schematically the detail of the grooves (73) of a grille (70) seen in section. A calender (70) includes an upper roller (71) and a lower roller (75). One of the rollers, for example the upper roller (71), comprises a crenellated part (72), while the other roller, that is to say the lower roller (75) in the example, comprises a grooved part (76), the shape of the grooves being complementary to the shape of the projecting parts (72) of the upper roller. The spacing E between the rollers (71), (75) and / or the pressure exerted by the two rollers against each other, makes it possible to define the dimensions of the grooves 73), and in particular their thickness ep and of width I. Each groove (73) is designed to accommodate a wick of fibers which is then pressed and heated between the rollers. The wicks are then transformed into parallel unidirectional ribbons whose thickness and width are calibrated by the grooves (73) of the calenders. Each grille advantageously comprises a plurality of grooves, the number of which can go up to 200, so as to produce as many ribbons as there are grooves and prepreg wicks. The calendering device further comprises a central device, referenced SYST in FIG. 1, controlled by a computer program provided for this purpose, which makes it possible to simultaneously regulate the pressure and / or the spacing of the calendering rollers of all the 100 unit calenders.
The unidirectional ribbon (s) thus manufactured has a width I and a thickness ep suitable for removal by robot in the manufacture of three-dimensional parts, without the need to be resold to the good width. The width of the ribbon (s) is advantageously between 5 and 400mm, preferably between 5 and 50mm, and even more preferably between 5 and 15mm.
The process for manufacturing a prepreg fibrous material which has just been described therefore makes it possible to produce prepreg fibrous materials with high productivity, while allowing impregnation in particular at the heart of the fibers and the control and reproducibility of the porosity, thus allowing control and reproducibility of the performance of the final composite article targeted. The impregnation in particular around the fibers and the absence of porosity are ensured by the impregnation step in the tank by controlling the residence time in the said powder, in particular a tank comprising a fluidized bed, and “effect of wedge ”, coupled to the simultaneous development of the wick at the level of the compression roller (s). The materials obtained are semi-finished products in the form of ribbons calibrated in thickness and in width, and having a low porosity.
The method therefore makes it possible to produce calibrated ribbons of prepreg fibrous material suitable for the production of three-dimensional composite parts, by automatic removal of said ribbons by means of a robot.
Advantageously, the thermoplastic polymer of the ribbon obtained with the process according to the invention is a polymer whose glass transition temperature is such that Tg> 80 ° C or a semi-crystalline polymer whose melting temperature Tf> 150 ° C.
Advantageously, said thermoplastic polymer is:
- an aliphatic polyamide chosen from polyamide 6 (PA-6), polyamide 11 (PA-11), polyamide 12 (PA-12), polyamide 66 (PA-66), polyamide 46 (PA-46) , polyamide 610 (PA-610), polyamide 612 (PA-612), polyamide 1010 (PA-1010), polyamide 1012 (PA-1012), mixtures thereof and copolyamides thereof , in particular 1010/11, 1010/12 etc ...
an aromatic polyamide, optionally modified by urea units, in particular a polyphthalamide, in particular a semi-aromatic polyamide of formula X / YAr, as described in EP1505099, in particular a semi-aromatic polyamide of formula A / XT in which A is chosen from a unit obtained from an amino acid, a unit obtained from a lactam and a unit corresponding to the formula (diamine in Ca). (diacid in Cb), with a representing the number of carbon atoms diamine and b representing the number of carbon atoms of the diacid, a and b each being between 4 and 36, advantageously between 9 and 18;
XT denotes a motif obtained from the polycondensation of a Cx diamine and terephthalic acid, with x representing the number of carbon atoms of the Cx diamine, x being between 6 and 36, advantageously between 9 and 18, in particular a polyamide of formula A / 6T, A / 9T, A / 10T or A / 11T, A being as defined above, in particular a polyamide PA 6 / 6T, 66 / 6T, 6I / 6T, PA11 / 10T, 11 / 6T / 10T, MXDT / 10T or MPMDT / 10T, BACT / 10T aramid, and block copolymers, in particular polyamide / polyether (PEBA).
Advantageously, the fibrous material of the ribbon obtained with the process according to the invention is made of carbon fiber.
Advantageously, the thermoplastic polymer of the ribbon obtained with the process according to the invention is a semi-aromatic polyamide, in particular chosen from PA 11, PA 12, PA 11/1010, PA 12/1010, PA 11 / 10T, PA 11 / 6T / 10T, PA MXDT / 10T, PA MPMDT / 10T and PA BACT / 10T and the fibrous material of the ribbon obtained with the process according to the invention is made of carbon fiber.
Advantageously, said tape, the thermoplastic polymer of which is a polyamide chosen from PA 11, PA 12, PA 11/1010, PA 12/1010, PA11 / 10T, PA 11 / 61710T, PA MXDT / 10T, PA MPMDT / 10T and PA BACT / 10T is used for civil or military aeronautics or the automobile.
Advantageously, the thermoplastic polymer of the ribbon obtained with the process according to the invention is PEKK.
Advantageously, the fibrous material of the ribbon obtained with the process according to the invention is made of carbon fiber.
Advantageously, the thermoplastic polymer of the ribbon obtained with the process according to the invention is PEKK and the fibrous material of the ribbon obtained with the process according to the invention is made of carbon fiber.
Advantageously, the thermoplastic polymer of the ribbon obtained with the process according to the invention is PEI.
Advantageously, the fibrous material of the ribbon obtained with the process according to the invention is made of carbon fiber.
Advantageously, the thermoplastic polymer of the ribbon obtained with the process according to the invention is PEI and the fibrous material of the ribbon obtained with the process according to the invention is made of carbon fiber.
Advantageously, the thermoplastic polymer of the ribbon obtained with the process according to the invention is a mixture of PEKK and PEI, preferably 90-10% to 60-40% in particular from 90-10% to 70-30% by weight.
Advantageously, the fibrous material of the ribbon obtained with the process according to the invention is made of carbon fiber.
Advantageously, the thermoplastic polymer of the ribbon obtained with the process according to the invention is a mixture of PEKK and PEI and the fibrous material of the ribbon obtained with the process according to the invention is made of carbon fiber.
According to another aspect, the present invention relates to the use of the ribbon of prepreg fibrous material, as defined above, in the manufacture of three-dimensional composite parts.
Advantageously, said manufacturing of said composite parts relates to the fields of transport, in particular automobile, oil and gas, in particular offshore, gas storage, civil or military aeronautics, nautical, rail; renewable energies, in particular wind, tidal, energy storage devices, solar panels; thermal protection panels; sports and leisure, health and medical, ballistics with parts for weapons or missiles, security and electronics.
According to yet another aspect, the present invention relates to a three-dimensional composite part, characterized in that it results from the use of at least one unidirectional tape of prepreg fibrous material as defined above.
Advantageous embodiments of the process of the invention
Advantageously, the fibrous material is chosen from carbon fiber and glass fiber.
Advantageously, the thermoplastic polymer used to impregnate the carbon fiber is chosen from a polyamide, in particular an aliphatic polyamide such as PA 11, PA 12, PA 11/1010 or PA 12/1010, or a semi-aromatic polyamide, in particular a PA 11 / 10T, PA 11 / 6T / 10T, PA MXDT / 10T or PA MPMDT / 10T, or PA BACT / 10T, PEKK and PEI or a mixture thereof.
Advantageously, the thermoplastic polymer used to impregnate the glass fiber is chosen from a polyamide, in particular an aliphatic polyamide such as
PA 11, PA 12, PA 11/1010 or PA 12/1010, or a semi-aromatic polyamide, in particular a PA11 / 10T, a PA 11 / 6T / 10T, a PA MXDT / 10T, a PA MPMDT / 10T, or PA BACT / 10T, a PEKK and a PEI or a mixture of these.
Advantageously, the content of fibers in said fibrous material, consisting of carbon or glass fiber, impregnated is between 45 and 65% by volume, preferably from 50 to 60% by volume, in particular from 54 to 60% by volume. volume.
Table I below groups together advantageous embodiments according to the method of the invention carried out in a tank comprising a fluidized bed for a wick made of carbon fiber or fiberglass with one or more cylindrical compression roller (s) ( s) not grooved:
Embodiment no. Fibrous material (fiber of ..) Polymer Number of compression rollers Residence time (s) Angle ai (°) 1 Carbon Polyamide 1 0.1 to 5 5 to 85 2 Carbon Polyamide 1 0.1 to 5 5 to 45 3 Carbon Polyamide 1 0.1 to 5 5 to 30 4 Carbon Polyamide 1 0.1 to 3 5 to 85 5 Carbon Polyamide 1 0.1 to 3 5 to 45 6 Carbon Polyamide 1 0.1 to 3 5 to 30 7 Carbon Polyamide 2 0.1 to 5 5 to 85 8 Carbon Polyamide 2 0.1 to 5 5 to 45 9 Carbon Polyamide 2 0.1 to 5 5 to 30 10 Carbon Polyamide 2 0.1 to 3 5 to 85 11 Carbon Polyamide 2 0.1 to 3 5 to 45 12 Carbon Polyamide 2 0.1 to 3 5 to 30 13 Carbon Polyamide 3 0.1 to 5 5 to 85 14 Carbon Polyamide 3 0.1 to 5 5 to 45 15 Carbon Polyamide 3 0.1 to 5 5 to 30 16 Carbon Polyamide 3 0.1 to 3 5 to 85 17 Carbon Polyamide 3 0.1 to 3 5 to 45 18 Carbon Polyamide 3 0.1 to 3 5 to 30 19 Carbon PEKK 1 0.1 to 5 5 to 85
20 Carbon PEKK 1 0.1 to 5 5 to 45 21 Carbon PEKK 1 0.1 to 5 5 to 30 22 Carbon PEKK 1 0.1 to 3 5 to 85 23 Carbon PEKK 1 0.1 to 3 5 to 45 24 Carbon PEKK 1 0.1 to 3 5 to 30 25 Carbon PEKK 2 0.1 to 5 5 to 85 26 Carbon PEKK 2 0.1 to 5 5 to 45 27 Carbon PEKK 2 0.1 to 5 5 to 30 28 Carbon PEKK 2 0.1 to 3 5 to 85 29 Carbon PEKK 2 0.1 to 3 5 to 45 30 Carbon PEKK 2 0.1 to 3 5 to 30 31 Carbon PEKK 3 0.1 to 5 5 to 85 32 Carbon PEKK 3 0.1 to 5 5 to 45 33 Carbon PEKK 3 0.1 to 5 5 to 30 34 Carbon PEKK 3 0.1 to 3 5 to 85 35 Carbon PEKK 3 0.1 to 3 5 to 45 36 Carbon PEKK 3 0.1 to 3 5 to 30 37 Carbon PEI 1 0.1 to 5 5 to 85 38 Carbon PEI 1 0.1 to 5 5 to 45 39 Carbon PEI 1 0.1 to 5 5 to 30 40 Carbon PEI 1 0.1 to 3 5 to 85 41 Carbon PEI 1 0.1 to 3 5 to 45 42 Carbon PEI 1 0.1 to 3 5 to 30 43 Carbon PEI 2 0.1 to 5 5 to 85 44 Carbon PEI 2 0.1 to 5 5 to 45 45 Carbon PEI 2 0.1 to 5 5 to 30 46 Carbon PEI 2 0.1 to 3 5 to 85 47 Carbon PEI 2 0.1 to 3 5 to 45 48 Carbon PEI 2 0.1 to 3 5 to 30 49 Carbon PEI 3 0.1 to 5 5 to 85 50 Carbon PEI 3 0.1 to 5 5 to 45 51 Carbon PEI 3 0.1 to 5 5 to 30 52 Carbon PEI 3 0.1 to 3 5 to 85
53 Carbon PEI 3 0.1 to 3 5 to 45 54 Carbon PEI 3 0.1 to 3 5 to 30 55 Carbon PEI 1 0.1 to 5 5 to 85 56 Carbon PEI 1 0.1 to 5 5 to 45 57 Carbon PEI 1 0.1 to 5 5 to 30 58 Carbon PEI 1 0.1 to 3 5 to 85 59 Carbon PEI 1 0.1 to 3 5 to 45 60 Carbon PEI 1 0.1 to 3 5 to 30 61 Carbon PEI 2 0.1 to 5 5 to 85 62 Carbon PEI 2 0.1 to 5 5 to 45 63 Carbon PEI 2 0.1 to 5 5 to 30 64 Carbon PEI 2 0.1 to 3 5 to 85 65 Carbon PEI 2 0.1 to 3 5 to 45 66 Carbon PEI 2 0.1 to 3 5 to 30 67 Carbon PEI 3 0.1 to 5 5 to 85 68 Carbon PEI 3 0.1 to 5 5 to 45 69 Carbon PEI 3 0.1 to 5 5 to 30 70 Carbon PEI 3 0.1 to 3 5 to 85 71 Carbon PEI 3 0.1 to 3 5 to 45 72 Carbon PEI 3 0.1 to 3 5 to 30 73 Glass Polyamide 1 0.1 to 5 5 to 85 74 Glass Polyamide 1 0.1 to 5 5 to 45 75 Glass Polyamide 1 0.1 to 5 5 to 30 76 Glass Polyamide 1 0.1 to 3 5 to 85 77 Glass Polyamide 1 0.1 to 3 5 to 45 78 Glass Polyamide 1 0.1 to 3 5 to 30 79 Glass Polyamide 2 0.1 to 5 5 to 85 80 Glass Polyamide 2 0.1 to 5 5 to 45 81 Glass Polyamide 2 0.1 to 5 5 to 30 82 Glass Polyamide 2 0.1 to 3 5 to 85 83 Glass Polyamide 2 0.1 to 3 5 to 45 84 Glass Polyamide 2 0.1 to 3 5 to 30 85 Glass Polyamide 3 0.1 to 5 5 to 85
86 Glass Polyamide 3 0.1 to 5 5 to 45 87 Glass Polyamide 3 0.1 to 5 5 to 30 88 Glass Polyamide 3 0.1 to 3 5 to 85 89 Glass Polyamide 3 0.1 to 3 5 to 45 90 Glass Polyamide 3 0.1 to 3 5 to 30 91 Glass PEKK 1 0.1 to 5 5 to 85 92 Glass PEKK 1 0.1 to 5 5 to 45 93 Glass PEKK 1 0.1 to 5 5 to 30 94 Glass PEKK 1 0.1 to 3 5 to 85 95 Glass PEKK 1 0.1 to 3 5 to 45 96 Glass PEKK 1 0.1 to 3 5 to 30 97 Glass PEKK 2 0.1 to 5 5 to 85 98 Glass PEKK 2 0.1 to 5 5 to 45 99 Glass PEKK 2 0.1 to 5 5 to 30 100 Glass PEKK 2 0.1 to 3 5 to 85 101 Glass PEKK 2 0.1 to 3 5 to 45 102 Glass PEKK 2 0.1 to 3 5 to 30 103 Glass PEKK 3 0.1 to 5 5 to 85 104 Glass PEKK 3 0.1 to 5 5 to 45 105 Glass PEKK 3 0.1 to 5 5 to 30 106 Glass PEKK 3 0.1 to 3 5 to 85 107 Glass PEKK 3 0.1 to 3 5 to 45 108 Glass PEKK 3 0.1 to 3 5 to 30 109 Glass PEI 1 0.1 to 5 5 to 85 110 Glass PEI 1 0.1 to 5 5 to 45 111 Glass PEI 1 0.1 to 5 5 to 30 112 Glass PEI 1 0.1 to 3 5 to 85 113 Glass PEI 1 0.1 to 3 5 to 45 114 Glass PEI 1 0.1 to 3 5 to 30 115 Glass PEI 2 0.1 to 5 5 to 85 116 Glass PEI 2 0.1 to 5 5 to 45 117 Glass PEI 2 0.1 to 5 5 to 30 118 Glass PEI 2 0.1 to 3 5 to 85
119 Glass PEI 2 0.1 to 3 5 to 45 120 Glass PEI 2 0.1 to 3 5 to 30 121 Glass PEI 3 0.1 to 5 5 to 85 122 Glass PEI 3 0.1 to 5 5 to 45 123 Glass PEI 3 0.1 to 5 5 to 30 124 Glass PEI 3 0.1 to 3 5 to 85 125 Glass PEI 3 0.1 to 3 5 to 45 126 Glass PEI 3 0.1 to 3 5 to 30 127 Glass PEI 1 0.1 to 5 5 to 85 128 Glass PEI 1 0.1 to 5 5 to 45 129 Glass PEI 1 0.1 to 5 5 to 30 130 Glass PEI 1 0.1 to 3 5 to 85 131 Glass PEI 1 0.1 to 3 5 to 45 132 Glass PEI 1 0.1 to 3 5 to 30 133 Glass PEI 2 0.1 to 5 5 to 85 134 Glass PEI 2 0.1 to 5 5 to 45 135 Glass PEI 2 0.1 to 5 5 to 30 136 Glass PEI 2 0.1 to 3 5 to 85 137 Glass PEI 2 0.1 to 3 5 to 45 138 Glass PEI 2 0.1 to 3 5 to 30 139 Glass PEI 3 0.1 to 5 5 to 85 140 Glass PEI 3 0.1 to 5 5 to 45 141 Glass PEI 3 0.1 to 5 5 to 30 142 Glass PEI 3 0.1 to 3 5 to 85 143 Glass PEI 3 0.1 to 3 5 to 45 144 Glass PEI 3 0.1 to 3 5 to 30
TABLE I
In the embodiments comprising PEKK or PEI, the PEKK can be mixed with PEI and the PEI can be mixed with PEKK in the proportions defined above.
Advantageously, in the compositions of table I above defined in which two compression rollers are present in the fluidized bed, the roller R2 is above the roller Ri relative to the bottom of the tank, in particular H2-H1 is included from 1cm to 30cm, preferably from 1 to 10cm, in particular from 1cm to 3cm, in particular about 2cm and the angle a ₂ is comprised from 0 to 90 °, in particular from 25 to 45 ° C, in particular from 25 to 35 ° and the wick passes over R ₂ .
These embodiments correspond to FIG. 5.
Advantageously, in the compositions of table I above defined in which two compression rollers are present in the fluidized bed, the roller R ₂ is above the roller Ri relative to the bottom of the tank, in particular H ₂ -Hi is from 1cm to 30cm, in particular about 2cm and the angle a ₂ is from 90 to 180 ° C, in particular from 115 to 135 °, especially from 115 to 125 °, and the wick passes below R ₂ .
Advantageously, in the compositions of Table I above, when the fibrous material is made of glass fiber, then the ratio D50 / average diameter of the unit fibers is comprised from 3 to 15, in particular from 4 to 15.
Advantageously, in the compositions of Table I above, when the fibrous material is made of glass fiber, then the ratio D50 / average diameter of the unit fibers is comprised from 3 to 10, in particular from 4 to 10.
Advantageously, in the compositions of Table I above, when the fibrous material is made of carbon fiber, then the ratio D50 / average diameter of the unit fibers is comprised from 10 to 40.
Advantageously, in the compositions of Table I above defined in which two compression rollers are present in the fluidized bed, the roller R ₂ is above the roller Ri with respect to the bottom of the tank, in particular H2 -H1 is included from 1cm to 3cm, in particular approximately 2cm and the angle a2 is included from 25 to 45 ° C, in particular from 25 to 35 ° and the wick passes above R ₂ ; and when the fibrous material is made of glass fiber, then the ratio D50 / average diameter of the unit fibers is comprised from 3 to 15, in particular from 4 to 15, in particular comprised from 3 to 10, in particular from 4 to 10.
Advantageously, in the compositions of table I above defined in which two compression rollers are present in the fluidized bed, the roller R ₂ is above the roller Ri relative to the bottom of the tank, in particular H ₂ -Hi is from 1cm to 3cm, in particular about 2cm and the angle a2 is from 80 to 45 ° C, in particular from 60 to 45 ° and the wick goes below R ₂ , and when the fibrous material is made of fiber glass then the report
D50 / average diameter of the unit fibers is from 3 to 15, in particular from 4 to
15, in particular ranging from 3 to 10, in particular from 4 to 10.
Advantageously, in the compositions of table I above defined in which two compression rollers are present in the fluidized bed, the roller R ₂ is above the roller Ri relative to the bottom of the tank, in particular H ₂ -Hi is included from 1cm to 3cm, in particular approximately 2cm and the angle a2 is included from 25 to 45 ° C, in particular from 25 to 35 ° and the wick passes above R ₂ ; and when the fibrous material is carbon fiber, then the ratio D50 / average diameter of the unit fibers is between 10 and 40.
Advantageously, in the compositions of table I above defined in which two compression rollers are present in the fluidized bed, the roller R ₂ is above the roller Ri relative to the bottom of the tank, in particular H ₂ -Hi is included from 1cm to 3cm, in particular approximately 2cm and the angle a2 is included from 80 to 45 ° C, in particular from 60 to 45 ° and the wick passes below R ₂ , and when the fibrous material is in fiber of carbon, then the ratio D50 / average diameter of the unit fibers is between 10 and 40.
Description of the figures
Figure 1 shows a diagram of a unit for implementing the process for manufacturing a prepreg fibrous material according to the invention.
Figure 2 shows a sectional diagram of two rollers constituting a calender as used in the unit of Figure 1.
Figure 3 details a tank (20) comprising a fluidized bed (22) with a fitting piece, adjustable in height (82). The edge of the tank inlet is equipped with a rotary roller 83a on which the wick 81a travels and the edge of the tank outlet is equipped with a rotary roller 83b on which the wick 81b travels.
FIG. 4 presents an embodiment with a single compression roller, with a tank (20) comprising a fluidized bed (22) in which a single cylindrical compression roller is present and showing the angle ai.
The arrows at the fiber indicate the direction of travel of the fiber.
FIG. 5 shows an embodiment, without being limited to this, with two compression rollers Ri and R ₂ , Ri preceding R ₂ , with a tank (20) comprising a fluidized bed (22) in which the two rollers of cylindrical compression are at different heights compared to the bottom of the tank (R ₂ at a height H ₂ above Ri at a height Hi) are present and showing the angle on eta ₂ .
The arrows at the fiber wick indicate the direction of travel of the wick.
FIG. 6 shows an exemplary embodiment with a tank (20) comprising a fluidized bed (22) in which the two compression rollers Ri and R ₂ are cylindrical, at the same level relative to each other and side by side and showing the angle ai, and the angle a ₂ = 0 ° and the wick passing between the 2 rollers)
FIG. 7 shows an exemplary embodiment with a tank (20) comprising a fluidized bed (22) in which the two compression rollers Ri and R ₂ are cylindrical, at the same level relative to each other and side by side and showing the angle ai, and the angle a ₂ = 90 ° and the wick passing below R ₂ .
FIG. 8 presents an exemplary embodiment with a tank (20) comprising a fluidized bed (22) in which two cylindrical compression rollers Ri and R ₂ , Ri preceding R ₂ , at different levels are present and showing the angle at and at ₂ and the drill bit passing under the roller R2.
FIG. 9 shows an embodiment with a tank (20) comprising a fluidized bed (22) with two compression rollers Ri and R ₂ , Ri preceding R ₂ , and a compression roller R3 and showing the angles on, a ₂ and 03.
Figure 10 shows a photo taken with a scanning electron microscope of a sectional view of a wick of carbon fiber% ”(Toray 12K T700S Μ0Ε fiber, diameter 7pm), impregnated with a polyamide PA MPMDT / 10T powder of D50 = 115pm according to the method of the invention (as described in Example 2, after calendering).
Image analysis gives a porosity rate of 5% excluding the edges of the tape. The ratio D50 / diameter = 16.4.
Figure 11 presents a photo taken with the scanning electron microscope of a sectional view of a wick of carbon fiber% ”(Toray fiber 12K T700, diameter 7pm) impregnated with a polyamide powder PA 11 / 6T / 10T of D50 = 132pm according to the method of the invention (as described in Example 2, after calendering).
The ratio D50 / diameter = 18.9.
Figure 12 shows a photo taken with a scanning electron microscope of a sectional view of a 3B HiPer Tex 2400 tex fiberglass wick (diameter
17pm), impregnated with a polyamide powder PA 11 of D50 = 120pm according to the method of the invention (as described in Example 3, before calendering).
The ratio D50 / diameter = 7.
Figure 13 presents a photo taken with the scanning electron microscope of a sectional view of a wick of 3B HiPer Tex 2400 tex fiberglass (diameter 17pm), impregnated with a polyamide powder PA 11 / 6T / 10T of D50 = 132pm according to the method of the invention (as described in Example 3, after calendering).
The ratio D50 / diameter = 7.
Figure 14 presents a binocular photo of a section view of a wick of carbon fiber% ”(SGL grade AA, 50K, diameter 7pm) impregnated with a polyamide powder MPMDT / 10T with D50 = 115pm according to the process of the invention (as described in Example 4, after calendering).
The ratio D50 / diameter = 16.4.
Figure 15 presents a photo taken with the scanning electron microscope of a sectional view of a wick of carbon fiber% ”(Toray fiber 12K T700, diameter 7pm) impregnated with a polyamide powder PA 11 of D50 = 20pm according to the process of the invention (as described in Example 2, before calendering).
The ratio D50 / diameter = 2.8.
FIG. 16 shows a photo taken with a scanning electron microscope of a sectional view of a wick of 3B HiPer Tex 2400 tex fiberglass (diameter 17 μm), impregnated with a polyamide PA 11 powder of D50 = 30 μm according to the process of the invention (as described in Example 2, before calendering).
The ratio D50 / diameter = 1.8.
Figure 17 shows the fluidization as a function of the air flow. The air flow applied to the fluidized bed must be between the minimum fluidization flow (Umf) and the minimum bubbling flow (Umf)
The following examples illustrate, without limitation, the scope of the invention.
Example 1 (comparative example):
A wick of carbon fiber (Toray 12K T700S Μ0Ε, diameter 7pm), was impregnated with PA 11 / 6T / 10T with D50 = 20μΜ.
The ratio D50 / diameter = 2.8, or <3.
Results:
Example 1bis (comparative example):
A wick of fiberglass (3B Fiberglass 2400 tex, diameter 17pm), was impregnated with PA11 of D50 = 30pm.
The ratio D50 / diameter = 1.8, or <3.
The results are presented in FIG. 15 (PA 11 example 1) and 16 (PA11 example bis) show poor impregnation to the core, linked to the fact that the powder is too fine (and has a too tight size distribution) to be properly fluidized. . In particular, numerous instabilities are present in the fluidized bed (presence of bubbles) which disturb the impregnation process. In addition, in the examples (glass and carbon) the wick of fiber spread by the fluidized bed has difficulty in retaining the powder because of its small particle size.
Example 2: general procedure for impregnating a fibrous material (carbon fiber) with a polyamide powder in a fluidized bed with a single roller
The following procedure was carried out:
A cylindrical compression roller in the tank (L = 500 mm, W = 500mm, H = 600mm), diameter 25 mm.
0.3 sec residence time in powder
25 ° angle
Flourishing about 100% (i.e. a width multiplied by 2) for a 1/4 ”Toray carbon fiber wick, 12K T700S Μ0Ε, diameter 7pm D50 = 115 pm. (D10 = 49pm, D90 = 207pm) for the powder of MPMDT / 10T. D50 = 132 pm, (D10 = 72pm and D90 = 225pm) for the 11 / 6T / 10T powder. edge of the tank fitted with a fixed roller.
The ratio D50 / diameter = 14.1.
The fibrous material (wick of carbon fiber% ”) was pre-impregnated with a polyamide (PA 11 / 6T / 10T and MPMDT / 10T with a particle size defined above) were prepared according to this procedure and are presented in the Figures 10 and 11. Figure 10 corresponds to MPMDT / 10T, Figure 11 to PA 11 / 6T / 10T.
This demonstrates the effectiveness of the impregnation process with a dry powder in a fluidized bed with a compression roller and control of the residence time in the powder.
Example 3: general procedure for impregnating a fibrous material (fiberglass) with a polyamide powder (PA11 and 11 / 6T / 10T) in a fluidized bed with a single roller
The following procedure was carried out:
A fixed compression roller in the 6 mm diameter tank
Residence time of approximately 5 sec
45 ° alpha angle
D50 of the 120 μm PA11 powder (D10 = 60 μm and D90 = 210 μm).
D50 of the 120 μm PA11 powder (D10 = 60 μm and D90 = 210 μm). Edge of the tank fitted with a fixed roller.
The fibrous material (1200 tex fiberglass wick) was pre-impregnated with different polyamides (PA11 and 11 / 6T / 10T) according to this operating mode and are presented in FIGS. 12 and 13. FIG. 12 corresponds to PA11 and Figure 13 in PA11 / 6T / 10T.
This demonstrates the effectiveness of the impregnation process with a dry powder in a fluidized bed with a compression roller and control of the residence time in the powder.
EXAMPLE 4 General Procedure for Impregnating a Fibrous Material with a Polyamide Powder in a Fluidized Bed with Two Rollers
Two cylindrical compression rollers at a height difference H2 -H1 = 2 cm, in the tank (L = 500 mm, W = 500, H = 600), both having a diameter of 25 mm. Distance of the rollers about 1 cm (as shown in figure 5)
2 sec residence time in powder
25 ° angle and 30 ° angle 02
Flourishing about 100% (i.e. a width multiplied by 2) for a 1/2 ”SGL grade AA carbon fiber wick
D50 of 98.9 pm powder.
edge of the tank fitted with a rotating roller.
The fibrous material (wick of carbon fiber (%) prepreg with a polyamide MPMDT / 10T) was prepared according to this procedure and is presented in Figure 14 (binocular view).
The impregnation rate is 40%.
This demonstrates the effectiveness of the impregnation process with a dry powder in a fluidized bed with two compression rollers and control of the residence time in the powder.
Example 5: Determination of the porosity rate by image analysis
The porosity was determined by image analysis on a wick of carbon fiber% "impregnated with MPMDT / 10T). It is 5%.
Example 6: Determination of the porosity rate the relative difference between theoretical density and experimental density (general method)
a) The required data are:
The density of the thermoplastic matrix
Fiber density
The grammage of the reinforcement:
• linear mass (g / m) for example for a% inch tape (from a single rowing) • surface mass (g / m ² ) for example for a wider tape or fabric
b) Measures to be carried out:
The number of samples must be at least 30 for the result to be representative of the material studied.
The measures to be carried out are:
The size of the samples taken:
o Length (if known linear density).
o Length and width (if known areal mass).
The experimental density of the samples taken:
o Mass measurements in air and water.
The measurement of the fiber content is determined according to ISO 1172: 1999 or by thermogravimetric analysis (ATG) as determined for example in the document B. Benzler, Applikationslabor, Mettler Toledo, Giesen, UserCom 1/2001.
Carbon fiber content measurement can be determined according to ISO
14127: 2008.
Determination of the theoretical mass fiber rate:
a) Determination of the theoretical mass fiber content:
With / 77 / the linear mass of the tape,
L the length of the sample and
Measure the mass of the sample measured in the air.
The variation in the mass content of fibers is assumed to be directly linked to a variation in the matrix rate without taking into account the variation in the quantity of fibers in the reinforcement.
b) Determination of the theoretical density:
^dth 1 -% Mf _{th +} % Mf _th

With dm and df the respective densities of the matrix and the fibers.
The theoretical density thus calculated is the density accessible if there is no porosity in the samples.
c) Evaluation of the porosity:
The porosity is then the relative difference between theoretical density and experimental density.

权利要求:
Claims (34)
[1" id="c-fr-0001]
1. A method of manufacturing a prepreg fibrous material comprising a fibrous material made of continuous fibers and at least one thermoplastic polymer matrix, characterized in that said prepreg fibrous material is produced in a single unidirectional ribbon or in a plurality of unidirectional parallel ribbons and in that said method comprises a step of impregnating, in particular at the heart, said fibrous material being in the form of a wick or of several parallel wicks by said thermoplastic polymer being in the form of powder, said step impregnation being carried out with said at least one thermoplastic polymer and said fibrous material whose ratio D90 / D10 by volume of the particles of thermoplastic polymer is between 1.5 and 50, in particular from 2 to 10 and the ratio of the mean diameter by volume (D50) of the thermoplastic polymer particles over the average diameter of the unitary fibers ires of said fibrous material is comprised from 3 to 40, excluding an aqueous suspension impregnation process of a fibrous material consisting of carbon fibers with a thermoplastic polymer and excluding any electrostatic charged process voluntary.
[2" id="c-fr-0002]
2. Method according to claim 1, characterized in that said fibrous material consists of glass fibers and said ratio D50 / average diameter of the unit fibers is from 3 to 15, in particular from 3 to 10.
[3" id="c-fr-0003]
3. Method according to claim 1, characterized in that said fibrous material consists of carbon fibers and said ratio D50 / average diameter of the unit fibers is from 10 to 40.
[4" id="c-fr-0004]
4. Method according to one of claims 1 to 3, characterized in that said impregnation step is carried out by powder deposition, fluidized bed or by spraying by means of spray gun (s) or nozzle (s) in roller inlet.
[5" id="c-fr-0005]
5. Method according to one of claims 1 to 4, characterized in that said impregnation step is carried out by dry process in a fluidized bed in a tank and the control of the rate of said at least one thermoplastic polymer matrix in said fibrous material is carried out by controlling the residence time of said fibrous material in the powder.
[6" id="c-fr-0006]
6. Method according to claim 5, characterized in that the fiber content in said impregnated fibrous material is between 45 and 65% by volume, preferably from 50 to 60% by volume, in particular from 54 to 60%.
[7" id="c-fr-0007]
7. Method according to claim 5 or 6, characterized in that the residence time in the powder is from 0.01 s to 10 s, preferably from 0.1 s to 5 s, and in particular from 0.1 s to 3 s.
[8" id="c-fr-0008]
8. Method according to one of claims 5 to 7, characterized in that said tank comprises a fluidized bed and said impregnation step is carried out with simultaneous development of said wick or said wicks between the inlet and the outlet of said fluidized bed .
[9" id="c-fr-0009]
9. Method according to claim 8, characterized in that said fluidized bed comprises at least one tying piece, said wick or said wicks being in contact with part or all of the surface of said at least one tying piece .
[10" id="c-fr-0010]
10. Method according to claim 9, characterized in that said development of said wick or said wicks is carried out at least at the level of said at least one fitting piece.
[11" id="c-fr-0011]
11. Method according to claim 9 or 10, characterized in that said at least one fitting piece is a compression roller of convex, concave or cylindrical shape.
[12" id="c-fr-0012]
12. The method of claim 11, characterized in that said at least one compression roller is of cylindrical shape and the percentage of development of said wick or said wicks between the inlet and the outlet of said fluidized bed being comprised of 1% at 400%, preferably between 30% and 400% preferably between 30% and 150%, preferably between 50% and 150%.
[13" id="c-fr-0013]
13. The method of claim 12, characterized in that a single compression roller is present in the fluidized bed and said impregnation is carried out at the angle ch formed by said wick or said wicks between the inlet of said compression roller and the vertical tangent to said compression roller.
[14" id="c-fr-0014]
14. The method of claim 13, characterized in that the angle is comprised from 0 to 89 °, preferably 5 ° to 85 °, preferably from 5 ° to 45 °, preferably from 5 ° to 30 °.
[15" id="c-fr-0015]
15. The method of claim 12, characterized in that two compression rollers Ri and R2 are present in said fluidized bed and said impregnation is carried out at the angle formed by said wick or said wicks between the inlet of said roller of compression Ri and the vertical tangent to said compression roller and / or at the level of the angle 02 formed by said wick or said wicks between the inlet of said compression roller R2 and the vertical tangent to said compression roller R2, said roller compression Ri (in the direction of travel of the process) preceding said compression roller R2 and said wick or said wick being able to pass above or below roller R2.
[16" id="c-fr-0016]
16. The method of claim 15, characterized in that the two compression rollers Ri and R2 are spaced 0.15 mm to the length equivalent to the maximum dimension of the tank, preferably spaced from 10mm to 50mm and in that the height difference between the two compression rollers Ri and R2 is between 0 and the height corresponding to the maximum height of the tank subtracted from the diameters of the two compression rollers, preferably between 0.15mm and the height corresponding to the maximum height of the tank subtracted from the diameters of the two compression rollers, more preferably at a height difference of between 10mm and 300mm, R2 being the upper compression roller.
[17" id="c-fr-0017]
17. Method according to one of claims 1 to 16, characterized in that a single thermoplastic polymer matrix is used and the thermoplastic polymer powder is fluidizable.
[18" id="c-fr-0018]
18. Method according to one of claims 1 to 17, characterized in that it further comprises a step of shaping said wick or said parallel wicks of said impregnated fibrous material, by calendering by means of at least one calender (51, 52, 53) heating in the form of a single unidirectional ribbon or of a plurality of parallel unidirectional ribbons with, in the latter case, said heating calender comprising a plurality of calendering grooves (73), preferably up to 200 calendering grooves, in accordance with the number of said ribbons and with a pressure and / or a spacing between the rollers of said calender regulated by a controlled system.
[19" id="c-fr-0019]
19. The method of claim 18, characterized in that the calendering step is carried out by means of a plurality of heating calenders (51, 52, 53), mounted in parallel and / or in series with respect to the direction of travel. strands of fiber.
[20" id="c-fr-0020]
20. Method according to one of claims 18 or 19, characterized in that said (or said) heating calender (s) comprises (include) a heating system integrated by induction or by microwaves, preferably by microwaves, coupled to the presence of carbonaceous fillers in said thermoplastic polymer or mixture of thermoplastic polymers.
[21" id="c-fr-0021]
21. Method according to one of claims 18 to 20, characterized in that said (or said) heating calender (s) is (are) coupled (s) to a rapid complementary heating device (41, 42, 43), located before and / or after said (each) calender (51, 52, 53), in particular a microwave or induction heating device coupled to the presence of carbonaceous fillers in said polymer or in said mixture of polymers, or an infrared IR, or Laser heating device or by direct contact with another heat source such as a flame or hot gas.
[22" id="c-fr-0022]
22. Method according to one of claims 1 to 21, characterized in that said at least one impregnation step (s) is (are) completed by a step of covering said single wick or said plurality of wicks parallel after impregnation with the powder, said covering step being carried out before said calendering step, with a molten thermoplastic polymer, which may be identical to or different from said polymer in the form of powder in a fluidized bed, said molten polymer preferably being of the same nature as said polymer in the form of a powder in a fluidized bed, preferably with said covering being effected by extrusion at a right angle relative to said single wick or to said plurality of parallel wicks.
[23" id="c-fr-0023]
23. Method according to one of claims 1 to 22, characterized in that said thermoplastic polymer further comprises carbonaceous fillers, in particular carbon black or carbonaceous nanofillers, preferably chosen from carbonaceous nanofillers, in particular graphenes and / or carbon nanotubes and / or carbon nanofibrils or their mixtures.
[24" id="c-fr-0024]
24. Method according to one of claims 1 to 23, characterized in that said thermoplastic polymer further comprises liquid crystal polymers or cyclized poly (butylene terephthalate), or mixtures containing them as additives.
[25" id="c-fr-0025]
25. Method according to one of claims 1 to 24, characterized in that said at least thermoplastic polymer is selected from: polyaryl ether ketones (PAEK), in particular poly (ether ether ketone) (PEEK); polyaryl ether ketone ketone (PAEKK), in particular poly (ether ketone ketone) (PEKK); aromatic polyether imides (PEI); polyaryl sulfones, in particular polyphenylene sulfones (PPSU); polyarylsulfides, in particular polyphenylene sulfides (PPS); polyamides (PA), in particular aromatic polyamides optionally modified by urea units; PEBAs, polyacrylates, in particular polymethyl methacrylate (PMMA); polyolefins, in particular polypropylene, polylactic acid (PLA), polyvinyl alcohol (PVA), and fluorinated polymers in particular polyvinylidene fluoride (PVDF) or polytetrafluoroethylene (PTFE) or polychlorotrifluoroethylene (PCTFE); and their mixtures, in particular a mixture of PEKK and PEI, preferably 90-10% to 60-40% in particular from 90-10% to 70-30% by weight.
[26" id="c-fr-0026]
26. The method of claim 25, characterized in that said at least thermoplastic polymer is a polymer whose glass transition temperature is such that Tg> 80 ° C or a semi-crystalline polymer whose melting temperature Tf> 150 ° C .
[27" id="c-fr-0027]
27. Method according to one of claims 1 to 26, characterized in that said fibrous material comprises continuous fibers selected from carbon, glass, silicon carbide, basalt, silica fibers, natural fibers in particular of flax or hemp, of lignin, of bamboo, of sisal, of silk, or of cellulose in particular of viscose, or of the amorphous thermoplastic fibers of glass transition temperature Tg greater than the Tg of said polymer or of said mixture of polymers when the latter is amorphous or greater than the Tf of said polymer or of said mixture of polymers when the latter is semi-crystalline, or the semi-crystalline thermoplastic fibers with a melting temperature Tf greater than the Tg of said polymer or of said mixture of polymers when the latter is amorphous or higher than the Tf of said polymer or of said mixture of polymers when the latter is semi-crystalline, or a mixture of two or more urs of said fibers, preferably a mixture of carbon fibers, glass or silicon carbide, in particular carbon fibers.
[28" id="c-fr-0028]
28. Unidirectional tape of pre-impregnated fibrous material, in particular tape wound on a reel, characterized in that it is obtained by a process as defined according to one of claims 1 to 27.
[29" id="c-fr-0029]
29. Tape according to claim 28, characterized in that it has a width (I) and a thickness (ep) suitable for removal by robot in the manufacture of three-dimensional parts, without the need for slitting, and preferably a a width (I) of at least 5 mm and up to 400mm, preferably between 5 and 50 mm and even more preferably between 5 and 15mm.
[30" id="c-fr-0030]
30. Tape according to one of claims 28 or 29, characterized in that the thermoplastic polymer is a polyamide chosen from in particular an aliphatic polyamide such as PA 11, PA 12, 11/1010 or 12/1010 or a semi-aromatic polyamide chosen from PA 11 / 10T, PA 11 / 6T / 10T, PA MXDT / 10T, PA MPMDT / 10T and PA BACT / 10T.
[31" id="c-fr-0031]
31. Use of the method as defined according to one of claims 1 to 27, for the manufacture of calibrated ribbons suitable for the manufacture of three-dimensional composite parts, by automatic removal of said ribbons by means of a robot.
[32" id="c-fr-0032]
32. Use of the ribbon of prepreg fibrous material, as defined according to one of claims 28 to 30, in the manufacture of three-dimensional composite parts.
[33" id="c-fr-0033]
33. Use according to claim 32, characterized in that said manufacturing of said composite parts relates to the fields of transport, in particular automobile, oil and gas, in particular offshore, gas storage, civil or military aeronautics, nautical , railway; renewable energies, in particular wind, tidal, energy storage devices, solar panels; thermal protection panels; sports and leisure, health and medical, ballistics with parts for weapons or missiles, security and electronics.
5
[0034]
34. Three-dimensional composite part, characterized in that it results from the use of at least one unidirectional ribbon of pre-impregnated fibrous material as defined according to one of claims 28 to 30.
1/16

类似技术:

---

公开号 | 公开日 | 专利标题

---

EP3393738B1|2020-07-22|Process for manufacturing a fibrous material preimpregnated with thermoplastic polymer in a fluidized bed

---

FR3061068A1|2018-06-29|PROCESS FOR PRODUCING PRE-IMPREGNATED FIBROUS MATERIAL OF THERMOPLASTIC POLYMER IN THE FORM OF POWDER

---

FR3061069A1|2018-06-29|PROCESS FOR PRODUCING PRE-IMPREGNATED FIBROUS MATERIAL OF THERMOPLASTIC POLYMER IN THE FORM OF DRY POWDER

---

EP3418019B1|2020-05-20|Method for producing a fibrous material impregnated with thermoplastic polymer

---

FR3061067A1|2018-06-29|METHOD FOR MANUFACTURING PRE-IMPREGNATED FIBROUS MATERIAL OF THERMOPLASTIC POLYMER THROUGH PROJECTION

---

EP3617254A1|2020-03-04|Fibrous material impregnated with thermoplastic polymer

---

EP3418014B1|2020-07-01|Method for producing a fibrous material impregnated with thermoplastic polymer

---

EP3670130A1|2020-06-24|Method for producing a fibrous material impregnated with thermoplastic polymer

---

EP3768768A1|2021-01-27|Fibrous material impregnated with thermoplastic polymer having a thickness of less than or equal to 100mm and method for the production thereof

---

EP3670129A1|2020-06-24|Method for producing a fibrous material pre-impregnated with thermoplastic polymer in a fluidised bed

---

EP3670128A1|2020-06-24|Method for producing a fibrous material pre-impregnated with thermoplastic polymer in a fluidised bed

---

FR3102701A1|2021-05-07|Process for impregnating a fibrous material with an optimized system for refeeding and cleaning fine particles

---

FR3082771A1|2019-12-27|PROCESS FOR MANUFACTURING PRE-IMPREGNATED FIBROUS MATERIAL OF THERMOPLASTIC POLYMER IN A FLUIDIZED BED

同族专利:

---

公开号 | 公开日

---

CN110099776A|2019-08-06|

---

JP2020501949A|2020-01-23|

---

EP3558613A1|2019-10-30|

---

FR3061069B1|2020-05-01|

---

US20200122359A1|2020-04-23|

---

WO2018115738A1|2018-06-28|

---

KR20190095291A|2019-08-14|

引用文献:

---

公开号 | 申请日 | 公开日 | 申请人 | 专利标题

---

FR2600585A1|1986-06-30|1987-12-31|Galichon Jean|Process for the manufacture of heat-stable articles made of composite materials and the articles thus obtained|

---

WO2012164014A1|2011-06-01|2012-12-06|Hexcel Reinforcements|Veiled tape with improved resistance to delamination|

---

FR3017329A1|2014-02-13|2015-08-14|Arkema France|METHOD FOR MANUFACTURING PRE-IMPREGNATED FIBROUS MATERIAL OF FLUIDIZED BED THERMOPLASTIC POLYMER|

---

WO2016062896A1|2014-10-24|2016-04-28|Porcher Industries|Strands powdered by electrostatic method|

---

WO2016093248A1|2014-12-08|2016-06-16|日立化成株式会社|Epoxy resin composition, resin sheet, prepreg, metal foil with resin, metal substrate and power semiconductor device|

---

DE3375488D1|1982-07-28|1988-03-03|Ici Plc|Method of producing fibre-reinforced composition|

---

FR2579133B1|1985-03-25|1987-09-25|Atochem|FIBER REINFORCED THERMOPLASTIC POLYMER COMPOSITE MATERIAL, MANUFACTURING METHOD THEREOF|

---

FR2625705B1|1988-01-11|1990-04-27|Arjomari Prioux|REINFORCED THERMOPLASTIC MATERIAL SHEET AND PROCESS FOR PREPARING SAME|

---

DE3810598A1|1988-03-29|1989-10-12|Bayer Ag|COMPOSITIONS CONTAINING METAL FIBERS AND THE USE THEREOF FOR PRODUCING MOLDED PARTS FOR SHIELDING ELECTROMAGNETIC RADIATION|

---

US5171630A|1989-04-17|1992-12-15|Georgia Tech Research Corporation|Flexible multiply towpreg|

---

FR2648957B1|1989-06-22|1991-11-15|France Etat Armement|COMPOSITE MATERIAL WITH MODULAR CHARACTERISTICS BY PREPREGNATION OF CONTINUOUS FIBER|

---

EP1045749B1|1998-01-16|2003-04-16|Neopreg AG|Fiber coating method|

---

FR2858626B1|2003-08-05|2005-10-07|Atofina|SOFT SEMI AROMATIC POLYAMIDES WITH LOW HUMIDITY RESUME|

---

MX2009009837A|2007-03-21|2009-09-24|Technip France|Flexible duct for conveying hydrocarbons and having a reinforced maintain layer.|

---

FR2967371B1|2010-11-17|2014-04-25|Arkema France|METHOD FOR MANUFACTURING PRE-IMPREGNATED FIBROUS MATERIAL OF THERMOSETTING POLYMER|

---

FR2981653B1|2011-10-25|2014-08-22|Arkema France|THERMOPLASTIC COMPOSITE MATERIAL REINFORCED WITH SYNTHETIC FIBERS AND METHOD OF MANUFACTURE|FR3067968B1|2017-06-22|2020-11-06|Arkema France|FIBROUS MATERIAL IMPREGNATED WITH THERMOPLASTIC POLYMER|

---

FR3067962B1|2017-06-22|2020-11-06|Arkema France|METHOD OF MANUFACTURING A FIBROUS MATERIAL IMPREGNATED WITH THERMOPLASTIC POLYMER|

---

FR3067961B1|2017-06-22|2020-11-06|Arkema France|METHOD OF MANUFACTURING A FIBROUS MATERIAL IMPREGNATED WITH THERMOPLASTIC POLYMER|

---

FR3082771B1|2018-06-22|2021-11-19|Arkema France|METHOD OF MANUFACTURING A FIBROUS MATERIAL PRE-IMPREGNATED WITH THERMOPLASTIC POLYMER IN A FLUIDIZED BED|

---

CN109206842B|2018-08-20|2021-05-07|南昌大学|Preparation method of continuous carbon fiber polyether-ether-ketone composite material|

---

EP3670129A1|2018-12-18|2020-06-24|Arkema France|Method for producing a fibrous material pre-impregnated with thermoplastic polymer in a fluidised bed|

---

EP3670128A1|2018-12-18|2020-06-24|Arkema France|Method for producing a fibrous material pre-impregnated with thermoplastic polymer in a fluidised bed|

---

FR3102701A1|2019-11-06|2021-05-07|Arkema France|Process for impregnating a fibrous material with an optimized system for refeeding and cleaning fine particles|

---

FR3107466A1|2020-02-24|2021-08-27|Arkema France|MIXTURE OF NON-REACTIVE THERMOPLASTIC POLYMER AND REACTIVE THERMOPLASTIC POLYMER AND ITS USE FOR THE PREPARATION OF COMPOSITES|

法律状态:
2017-11-13| PLFP| Fee payment|Year of fee payment: 2 |

---

2018-06-29| PLSC| Search report ready|Effective date: 20180629 |

---

2019-11-14| PLFP| Fee payment|Year of fee payment: 4 |

---

2021-09-10| ST| Notification of lapse|Effective date: 20210806 |

优先权:

---

申请号 | 申请日 | 专利标题

---

FR1663209|2016-12-22|

---

FR1663209A|FR3061069B1|2016-12-22|2016-12-22|PROCESS FOR THE MANUFACTURE OF A PRE-IMPREGNATED FIBROUS MATERIAL OF THERMOPLASTIC POLYMER IN THE FORM OF DRY POWDER|FR1663209A| FR3061069B1|2016-12-22|2016-12-22|PROCESS FOR THE MANUFACTURE OF A PRE-IMPREGNATED FIBROUS MATERIAL OF THERMOPLASTIC POLYMER IN THE FORM OF DRY POWDER|

---

KR1020197016931A| KR20190095291A|2016-12-22|2017-12-20|Process for preparing fibrous material preimpregnated with thermoplastic polymer in dry powder form|

---

US16/471,876| US20200122359A1|2016-12-22|2017-12-20|Process for manufacturing a fibrous material pre-impregnated with thermoplastic polymer in dry powder form|

---

CN201780078449.1A| CN110099776A|2016-12-22|2017-12-20|With the manufacturing method of the fibrous material of the thermoplastic polymer pre-preg in dry powder form|

---

PCT/FR2017/053730| WO2018115738A1|2016-12-22|2017-12-20|Process for manufacturing a fibrous material preimpregnated with thermoplastic polymer in dry powder form|

---

EP17829262.9A| EP3558613A1|2016-12-22|2017-12-20|Process for manufacturing a fibrous material preimpregnated with thermoplastic polymer in dry powder form|

---

JP2019534175A| JP2020501949A|2016-12-22|2017-12-20|Method for producing fibrous material preimpregnated with thermoplastic polymer in dry powder form|