• 专利附录
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    • 专利摘要:
    The invention relates to the use of a composition comprising at least one semi-crystalline A / XYY copolyamide in which: A is a repeating unit obtained from the polycondensation of at least one C 6 to C 12 lactam, or at least one XY repeating unit obtained from the polycondensation of at least one C4 to C18 aliphatic diamine (X), and at least one C6 to C18 aliphatic (Y) dicarboxylic acid, in particular C6 to C18 aliphatic C12, X1Y is a repeating unit obtained from the polycondensation of a diamine (X1) selected from an arylamine, a cycloaliphatic diamine and a branched aliphatic diamine, and at least one aliphatic dicarboxylic acid (Y) identical to that of the XY pattern, the ratio by weight A / X1Y being between 60/40 and 95/5, circular section glass fibers, and optionally at least one impact modifier and / or at least one additive, to limit warping while keeping the cycle time of the resulting composition adapted to its implementation, in particular by injection.
    公开号:FR3071503A1
    申请号:FR1758829
    申请日:2017-09-25
    公开日:2019-03-29
    发明作者:Stefania Cassiano Gaspar；Benoit Brule
    申请人:Arkema France SA；
    IPC主号:
    专利说明:

    Use of a copolyamide composition as matrix of material loaded with circular section glass fibers to limit warping
    The present invention relates to the use of a semi-crystalline copolyamide, in particular semi-arylaliphatic, semi-alicyclic or semi-aliphatic branched, as matrix of a material loaded with glass fibers of circular section, to limit warping while keeping the cycle time of the composition obtained suitable for its implementation. It also relates to the composition obtained and its use for constituting a monolayer structure or at least one layer of a multilayer structure, in particular in the electrical and / or electronic (E / E) field.
    Many applications in the E / E field require very rigid materials (phone shell, computer part, etc.). Rigidity is all the more important as the market trend is towards a reduction in the weight of electronic equipment and therefore towards a reduction in the thicknesses of the parts.
    However, the production of thin parts brings other problems: ability to be injected, in particular materials which are sufficiently fluid to completely fill the mold and above all respect for the stability of the parts (absence of warping: major problem with these rigid materials obtained by adding glass fibers). It is also appropriate that the transformation (for example by injection) takes place in transformation times, in particular cycle times adapted to an industrial process.
    Warping is induced by internal stresses whose consequence (or relaxation) is the deformation of the part. In the case of heavily loaded materials, the orientation of the fibers in the direction of flow has the consequence of limiting the shrinkage in this direction. On the other hand, in the direction perpendicular to the axis of the fibers, the shrinkage is controlled by the polymer and is therefore greater. This differential shrinkage is the main source of warping. The case of polymers reinforced with high levels of glass fiber is clearly the case for which the warping aspect is critical.
    In these applications, rigid polyamides (PA) (module> 12GPa) find a great place. But as soon as the fiber content is greater than 25%, the use of fibers with a non-circular or flat cross-section (FF) is the solution chosen to satisfy all of the specifications, and in particular to limit warping. fine parts injected.
    Thus, application EP2789591, in paragraph [0003], indicates that glass fibers with a non-circular cross section make it possible to improve the mechanical properties, the dimensional stability and the warping of resins reinforced with said glass fibers of non-circular section. This is due, according to this request, as regards the improvement of the mechanical properties, to the fact that the glass fibers of non-circular section have a contact surface greater than that of the fibers of circular section. As regards the improvement of dimensional stability and warping, this is due, still according to application EP2789591, to the fact that glass fibers of non-circular section orient less in the direction of flow than the fibers of circular section glass and therefore tend to be more oriented in two dimensions than the circular section glass fibers in the injected part.
    Likewise, application US 2011/0105655 describes compositions having a low distortion during molding and consisting of 25 to 72% by weight of a polyamide, from 20 to 65% by weight of glass fibers with flat section of ratio L / D from 2 to 8, and from 8 to 25% by weight of a flame-retardant agent (L representing the large dimension of the cross section of the fiber and D the small dimension of the cross section of said fiber). The polyamide used is a mixture of 55-90% by weight of an aliphatic polyamide and from 10 to 45% by weight of another polyamide which may be MXD6 relative to the total sum of the polyamides.
    Also, the application US 2010/279111 describes compositions also having a low distortion during molding made up of 30 to 80% by weight of a polyamide and 20 to 70% of long glass fibers with flat section of L / D ratio from 2 to 8. The polyamide used is either a mixture of 55 to 85% by weight of an aliphatic polyamide and from 15 to 45% by weight of a polyamide which may be MXD6 relative to the total sum of the polyamides, or a mixture of 55 to 85% by weight of an aliphatic polyamide and from 15 to 45% by weight of a copolyamide comprising one or more polyamides, for example MXDI or MXD6 and at least one other polyamide chosen from PA 66, 610, 6 and 12, relative to the total sum of the polyamides.
    Patent JP5523520 describes polyamide granules having electrical properties and resistance to deformation.
    The granules consist of 5-40 parts by weight of a flame retardant, 5-200 parts by weight of a flat section fiberglass with an L / D ratio of at least 2.3 and 0- 40 parts by weight of a polyamide which can be a mixture of aliphatic polyamide with a semi-aromatic polyamide such as MXD10.
    However, the use of flat section glass fibers compared to circular section glass fibers generates a significant additional cost. In addition, the suppliers of flat section glass fibers are much less numerous than the suppliers of circular section glass fiber. These two aspects are essential in the industrial production of glass fiber reinforced resins.
    Document EP 1972659 describes compositions and articles for portable electronic devices. The examples presented show that compositions based on mixtures of polyamides PA66 and MXD6, predominantly in MXD6 (Example 1), are free from warping when flat section glass fibers are used. On the other hand, when circular section glass fibers are used (Comparative Example 2), the compositions exhibit significant warpage. This document does not deal with cycle time.
    Furthermore, document EP 2456822 teaches that the compositions based on MXD10, although having a good modulus, however, require a high mold temperature during their shaping by injection-molding to ensure maximum crystallization of the product and therefore confer properties. mechanical and dimensional stability.
    It is therefore necessary to be able to have compositions using glass fibers with circular section, and a copolyamide matrix thus making it possible to limit the cost of said composition and to ensure a perennial supply of glass fibers with circular section while limiting the drawback of these, namely in particular the warping induced by glass fibers during the use of compositions containing more than 25% of glass fibers, and by retaining sufficiently rapid kinetics of crystallization of the matrix to have transformation times, in particular sufficiently short cycle times during injection and easy demolding.
    These various problems have been solved by specific semi-crystalline, in particular semi-arylaliphatic, semi-alicyclic or semi-aliphatic branched copolyamides, as a matrix of a material loaded with glass fibers of circular cross section.
    The present invention therefore relates to the use of a composition comprising at least one semi-crystalline A / XiY copolyamide in which:
    - A is a repeating unit obtained from the polycondensation of at least one ameβ to C12 lactam, preferably C12, or at least one Οβ to C12 amino acid, preferably Cn, or at least a repeating unit XY obtained from the polycondensation of at least one aliphatic diamine (X) at C4 to Cw, in particular at C4 to C12 and at least one aliphatic dicarboxylic acid (Y) at Ü6 to Cw, in particular in Οβ to C12,
    - X1Y is a repeating unit obtained from the polycondensation of a diamine (X1) chosen from an arylamine, a cycloaliphatic diamine and a branched aliphatic diamine, and at least one aliphatic dicarboxylic acid (Y) identical to that of the unit XY, the weight ratio A / X1Y being comprised from 60/40 to 95/5, glass fibers of circular section, and optionally at least one impact modifier and / or at least one additive, to limit warping while keeping the cycle time of the composition obtained adapted to its implementation, in particular by injection.
    Throughout the description, the expression understood from ... to ... means that the limits are included.
    The inventors have unexpectedly found that the presence of a repeating unit X1Y based on an arylaliphatic, cycloaliphatic or aliphatic branched diamine, in a particular mass proportion in a composition comprising a semi-crystalline copolyamide A / X1Y and glass fibers with a circular section made it possible not only to limit the warpage of the composition compared to the linear aliphatic polyamide A alone during the processing, in particular by injection of the composition, but also to maintain an adapted cycle time during the setting while avoiding the mold ejection problems associated with incomplete crystallization of the composition.
    A semi-crystalline copolyamide, within the meaning of the invention, designates a copolyamide which has a melting temperature (Tf) in DSC according to ISO standard 11357-3: 2013, and an enthalpy of crystallization during the cooling step to a speed of
    20K / min in DSC measured according to ISO 11357-3 of 2013 greater than 30 J / g, preferably greater than 40 J / g.
    The nomenclature used to define polyamides is described in 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 in the art. skilled in the art.
    When the repeating unit A of said copolyamide is obtained from the polycondensation of a lactam, said lactam can be chosen from pyrrolidinone, 2-piperidinone, caprolactam, enantholactam, caprylolactam, pelargolactam, decanolactam, undecanolactam, and lauryllactame, in particular lauryllactame.
    When the repeating unit A of said copolyamide is obtained from the polycondensation of an amino acid, it can be chosen from 9 aminononanoic acid, 10-aminodecanoic acid, 10-aminoundecanoic acid, 12-aminododecanoic acid and 11-aminoundecanoic acid and its derivatives, in particular N-heptyl-11-aminoundecanoic acid, in particular 11 aminoundecanoic acid.
    When the repeating unit A of said copolyamide is obtained from the polycondensation of a repeating unit XY, the diamine (X) at C4 to Cw used in polyamide XY is a linear aliphatic diamine, and can in particular be chosen from 1 , 4-butanediamine, 1,5-pentamethylenediamine, 1,6-hexamethylenediamine 1,7-heptamethylediamine, 1,8-octamethylediamine, 1,9-nonamethylediamine,
    1,10-décaméthylèdiamine,
    1,11-undecamethylediamine, 1,12dodecamethylediamine, 1,13-tridecamethylediamine, 1,14tetradecamethylediamine,
    1,16-hexadecamethylediamine and the
    1,18octadécaméthylèdiamine.
    Advantageously, the diamine (X) used is in C4 to C12, in particular chosen from
    1,4-butanediamine, 1,5-pentamethylediamine, 1,6-hexamethylenediamine 1,7 heptamethylediamine, 1,8-octamethylediamine, 1,9-nonamethylediamine, 1,10 decamethylediamine, 1,11-undecamethylediamine, 1,12-dodecamethylediamine.
    Advantageously, the diamine (X) used is in Οβ to C10, in particular chosen from
    1,6-hexamethylenediamine 1,7-heptamethylediamine, 1,8-octamethylediamine,
    1,9-nonamethylèdiamine, 1,10-decamethylèdiamine.
    When the repeating unit A of said copolyamide is obtained from the polycondensation of a repeating unit XY, the aliphatic dicarboxylic acid (Y) at C6 to Cie can be chosen from adipic acid, suberic acid, acid azelaic, sebacic acid, undecanedioic acid, dodecanedioic acid, brassylic acid, tetradecanedioic acid, pentadecanedioic acid, hexadecanedioic acid, octadecanedioic acid.
    Advantageously, the aliphatic dicarboxylic acid (Y) is C6 to C12 and can be chosen from adipic acid, suberic acid, azelaic acid, sebacic acid, undecanedioic acid, dodecanedioic acid.
    The aliphatic diamine (X) can be mixed with one or more other aliphatic diamines X ’.
    Likewise, the aliphatic dicarboxylic acid (Y) can be mixed with one or more other aliphatic dicarboxylic acids Y ’.
    It is quite obvious in these last two cases that the repeating pattern XY containing X and / or Y ′ is in any case in mass proportion greater than or equal to 60%.
    On the other hand, a mixture of aliphatic repeating unit XY with one or more repeating units resulting from the polycondensation of lactams or of amino acid is excluded from the scope of the invention.
    As regards the repeating unit X1Y, the diamine (X1) is chosen from an arylamine, a cycloaliphatic diamine, and a branched aliphatic diamine.
    When the diamine (X1) is an arylamine, it can be chosen from meta-xylylene diamine (MXD, CAS number: 1477-55-0) or para-xylylene diamine (PXD, CAS number: 53948-0) .
    When the diamine (X1) is a cycloaliphatic diamine, it can be chosen from bis (3,5-dialkyl-4-aminocyclohexyl) -methane, bis (3,5-dialkyl-4aminocyclohexyl) ethane, bis (3, 5-dialkyl-4-aminocyclohexyl) -propane, bis (3,5dialkyl-4-aminocyclo-hexyl) -butane, bis- (3-methyl-4-aminocyclohexyl) -methane or 3,3'-dimethyl-4 , 4'-diamino-dicyclohexyl-methane commonly known (BMACM) or (MACM) (and noted B below), p-bis (aminocyclohexyl) -methane commonly known (PACM) (and noted P below), in particular Dicykan®, isopropylidenedi (cyclohexylamine) commonly known (PACP), isophoronediamine (noted IPD below) and 2,6-bis (amino methyl) norbornane commonly known (BAMN) and bis (aminomethyl ) cyclohexane "BAC).
    When this diamine (Xi) is a branched aliphatic diamine, it comes from an aliphatic diamine having a straight main chain comprising at least 4 carbon atoms and comprising one or more methyl and / or ethyl substituents.
    It can in particular be 2-methyl pentamethylenediamine (MPMD), 2-methyl1,8-octamethylenediamine (MOMD) or trimethylene (2,2,4 or 2,4,4) hexamethylenediamine (TMDA).
    The dicarboxylic acid (Y) of the repeating unit XiY is identical to that of the repeating unit XY and therefore as defined above.
    However, when the dicarboxylic acid of the repeating unit XY is in admixture with another dicarboxylic acid Y ’as described above, then the repeating unit XY’ is in minor mass proportion relative to the sum of XY and XY ’.
    Advantageously, the mass ratio XY / XY ’is comprised from 90/10 to 99.9 / 0.1.
    Likewise, when the dicarboxylic acid of the repeating unit XiY is in admixture with another dicarboxylic acid Y 'as described above, then the repeating unit XiY' is in a minority mass proportion relative to the sum of XiY and XIV.
    Advantageously, the mass ratio X1Y / X1Y ’is from 90/10 to 99.9 / 0.1.
    The weight ratio A / X1Y is from 60/40 to 95/5.
    Above 40% by weight of X1Y, the composition presents processing difficulties and in particular difficulties in ejecting the mold, a long cycle time due to the crystallization being too slow because it is too affected by the level of monomers and in particular incomplete.
    Below 5% by weight of X1Y, the composition exhibits warping. Advantageously, the weight ratio A / X1Y is from 70/30 to 95/5.
    By fiberglass in the sense of the invention is meant any glass fiber, in particular as described by Frederick T. Wallenberger, James C. Watson and Hong Li, PPG industries Inc. (ASM Handbook, Vol 21: composites (# 06781G), 2001 ASM International), provided that said fiber is of circular section.
    Advantageously, said glass fibers have a ratio L / D (L representing the large dimension of the cross section of the fiber and D the small dimension of the cross section of said fiber) less than 2, in particular less than 1.5.
    Advantageously, the L / D ratio is equal to approximately 1 and the diameter is from 4 μm to less than 25 μm, preferably from 4 to 15 μm.
    The expression “impact modifier” should be understood to mean a polyolefin-based polymer having a flexural modulus of less than 100 MPa measured at 23 ° C according to ISO standard 178: 2010 and of Tg less than 0 ° C (measured according to the standard 11357-2 at the inflection point of the DSC thermogram), in particular a polyolefin, coupled or not with a Peba (polyether block amide) having a flexural modulus <200 MPa. It would not go beyond the scope of the invention to use a Peba alone as a shock modifier in the composition.
    The polyolefin of the impact modifier can be functionalized or non-functionalized or be a mixture of at least one functionalized and / or at least one non-functionalized.
    In particular, some or all of the polyolefins carry a function chosen from the carboxylic acid, carboxylic anhydride and epoxide functions, and is in particular chosen from an ethylene-propylene copolymer of elastomeric character (EPR), an ethylene-propylene copolymer -diene with an elastomeric nature (EPDM) and an ethylene / (meth) alkyl acrylate copolymer, an ethylene-higher alkene copolymer, in particular an ethylene-octene copolymer, an ethylene-alkyl acrylate-maleic anhydride terpolymer.
    Advantageously, the impact modifier is chosen from Fusabond® F493, a Pebax®, in particular Pebax® 40R53 SP01, a Lotader®, in particular Lotader® 5500 or Lotader® 7500, Exxelor® VA1803, or a mixture of these, in this case they are in a ratio ranging from 0.1 / 99.9 to 99.9 / 0.1, preferably 1/2 to 2/1 when they are a mixture of two.
    By way of example, the impact modifier is chosen from the following mixtures: Fusabond® 493 / Lotader®, in particular Fusabond® 493 / Lotader® 5500 or Fusabond® 493 / Lotader® 7500.
    The impact modifier can also be a “core-shell” type modifier, also known as a “core-shell type copolymer”.
    The modifier of “core-shell” type is in the form of fine particles having an elastomer core and at least one thermoplastic shell, the particle size is generally less than μm and advantageously between 150 and 500 nm.
    The “core-shell” modifier has an acrylic or butadiene base, unlike the impact modifier, which has a polyolefin base.
    Advantageously, the proportion of impact modifier is between 0 and 10% by weight relative to the total weight of the composition.
    The additives optionally used in the composition of the invention are the conventional additives used in polyamides and well known to those skilled in the art such as fillers, dyes, stabilizers, plasticizers, surfactants, nucleating agents, pigments, brighteners, antioxidants, lubricants, flame retardants, waxes and their mixtures.
    Throughout the description, the term "filler" excludes glass fibers in any form.
    The expression "limit warping" means that warping is less than
    1.5 mm, in particular less than 1 mm as determined on 100 * 100 * 1 mm plates 3 , 7 days after processing.
    Warping can be completely eliminated, but as a rule it is less than 1.5 mm, in particular less than 1 mm.
    The expression "while keeping the cycle time of the composition obtained suitable for its implementation" means that the time necessary for the manufacture of a part from the composition of the invention is not too long.
    In particular, the cycle time per injection comprising the stages of injection, cooling, opening of the mold and ejection of the product formed, is carried out in less than 50 seconds, preferably in less than 40 seconds, in particular in less than 30 seconds.
    It would not be departing from the scope of the invention if the implementation were carried out by compression molding.
    Advantageously, the present invention relates to the use of a composition comprising at least one semi-crystalline A / XiY copolyamide in which:
    - A is a repeating unit obtained from the polycondensation of a lactam at Οδ to C12, preferably at C12, or an amino acid at Οβ to C12, preferably at C11, or from a repeating unit XY obtained at starting from the polycondensation of an aliphatic diamine (X) at C 4 to Cw, in particular at C 4 to C12 and an aliphatic dicarboxylic acid (Y) at Οβ to Cw, in particular at Οβ to C12,
    X1Y is a repeating unit obtained from the polycondensation of a diamine (X1) chosen from an arylamine, a cycloaliphatic diamine and a branched aliphatic diamine, and of an aliphatic dicarboxylic acid (Y) identical to that of the unit XY, the weight ratio A / X1Y being comprised from 60/40 to 95/5, glass fibers with circular section, and optionally at least one impact modifier and / or at least one additive, to limit warping while keeping the time cycle of the composition obtained suitable for its implementation, in particular by injection.
    The different repeating units are as defined above with the difference that the repeating unit A is obtained from the polycondensation of a single lactam, or of a single amino acid or of a single unit XY and that the unit XiY also corresponds to a single repeating pattern.
    Consequently, the copolyamide of this embodiment consists only of two repeating units.
    Advantageously, the present invention relates to the use of a composition as defined above, characterized in that said composition comprises:
    from 25 to 65% by weight, in particular from 35 to 65% of said at least one A / XiY copolyamide,
    - from 35 to 75% by weight, in particular from 35 to 65% by weight of glass fibers with circular section,
    - from 0 to 10% by weight of at least one impact modifier,
    - from 0 to 2% by weight of at least one additive, the sum of the proportions of each constituent of the composition being equal to 100%.
    In one embodiment, said arylamine of the XiY motif of said copolyamide of said composition is chosen from meta-xylylene diamine (MXD) and para-xylylene diamine (PXD).
    In another embodiment, said cycloaliphatic diamine of the XiY motif of said copolyamide of said composition is bis (aminomethyl) cyclohexane (BAC).
    The BAC can be 1,3-BAC or 1,4-BAC.
    1,3-BAC (or 1,3 bis (aminomethyl) cyclohexane, CAS No: 2579-20-6) is a cycloaliphatic diamine monomer obtained in particular by hydrogenation of metaxylylene diamine (MXD). 1,3-BAC exists in the form of two isomers, cis and trans, CAS No. 2579-20-6 corresponding to a mixture of isomers.
    1,4-BAC (or 1,4 bis (aminomethyl) cyclohexane, CAS No: 2549-07-9) is a cycloaliphatic diamine monomer obtained in particular by hydrogenation of paraxylylene diamine (PXD). 1,4-BAC exists in the form of two isomers, cis and trans, CAS No. 2549-07-9 corresponding to a mixture of isomers.
    Advantageously, the 1.3 BAC or the 1.4 BAC used in the composition of the invention is a mixture of cis and trans isomers in respective proportions from 0.1 / 99.9 to 99.9 / 0.1, especially from 75/25 to 25/75.
    It is understood that when the 1.3 BAC or the 1.4 BAC used in the composition of the invention is a mixture of cis and trans isomers, this does not correspond to a mixture of diamine Xi but to a single diamine Xi.
    Advantageously, the proportion of cis isomer in 1.3 BAC is greater than 60%, preferably greater than 70%, in particular greater than 80%, in particular greater than 90%.
    Advantageously, the proportion of trans isomer in 1.4 BAC is greater than 60%, preferably greater than 70%, in particular greater than 80%, in particular greater than 90%.
    In another embodiment, said branched aliphatic diamine is chosen from 2-methyloctanediamine (MOMD), methylpentamethylene diamine (MPMD) and trimethylhexamethylenediamine (TMDA).
    In an advantageous embodiment, said diamine (Xi) is chosen from metaxylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD). Advantageously, A is a repeating pattern XY.
    Advantageously, A is a repeating unit XY and said diamine (Xi) is chosen from meta-xylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD) ). In one embodiment, A is a repeating unit XY and (Y) is an aliphatic dicarboxylic acid (Y) at C6 to C12, in particular (Y) corresponds to sebacic acid.
    Advantageously, A is a repeating unit XY, (Y) being an aliphatic dicarboxylic acid (Y) at C6 to C12 and said diamine (X1) is chosen from meta-xylylene diamine (MXD), para-xylylene diamine (PXD) , bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, A is a repeating unit XY, (Y) corresponding to sebacic acid and said diamine (X1) is chosen from meta-xylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    In one embodiment, (X) corresponds to a Ü6 to C12 diamine, in particular hexamethylene diamine or decanediamine.
    Advantageously, A is a repeating unit XY, (Y) being an aliphatic dicarboxylic acid (Y) at Ü6 to C12 and (X) corresponds to a diamine at Ü6 to C12.
    Advantageously, A is a repeating unit XY, (Y) being an aliphatic dicarboxylic acid (Y) in Ü6 to C12 and (X) corresponds to hexamethylene diamine or decanediamine.
    Advantageously, A is a repeating unit XY, (Y) being an aliphatic dicarboxylic acid (Y) at Ü6 to C12, (X) corresponds to a diamine at Ü6 to C12 and said diamine (X1) is chosen from meta-xylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, A is a repeating unit XY, (Y) being sebacic acid or dodecanedioic acid, (X) corresponds to a C 6 to C 12 diamine and said diamine (X1) is chosen from meta-xylylene diamine (MXD ), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, A is a repeating unit XY, (Y) being sebacic acid, (X) corresponds to a C 6 to C 12 diamine and said diamine (X1) is chosen from metaxylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, A is a repeating unit XY, (Y) being dodecanedioic acid, (X) corresponds to a C 6 to C 12 diamine and said diamine (X1) is chosen from metaxylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, A is a repeating unit XY, (Y) being an aliphatic dicarboxylic acid (Y) at C6 to C12, (X) corresponds to hexamethylene diamine or decanediamine and said diamine (X1) is chosen from meta-xylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, A is a repeating unit XY, (Y) being sebacic acid or dodecanedioic acid, (X) corresponds to hexamethylene diamine or decanediamine and said diamine (X1) is chosen from meta-xylylene diamine ( MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, A is a repeating unit XY, (Y) being sebacic acid, (X) corresponds to hexamethylene diamine or decanediamine and said diamine (Xi) is chosen from meta-xylylene diamine (MXD), para -xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD). Advantageously, A is a repeating unit XY, (Y) being sebacic acid, (X) corresponds to hexamethylene diamine and said diamine (Xi) is chosen from metaxylylene diamine (MXD), para-xylylene diamine (PXD ), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD). Advantageously, A is a repeating unit XY, (Y) being sebacic acid, (X) corresponds to decanediamine and said diamine (Xi) is chosen from metaxylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, A is a repeating unit XY, (Y) being dodecanedioic acid, (X) corresponds to hexamethylene diamine or decanediamine and said diamine (Xi) is chosen from meta-xylylene diamine (MXD), para -xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, A is a repeating unit XY, (Y) being dodecanedioic acid, (X) corresponds to hexamethylene diamine and said diamine (Xi) is chosen from metaxylylene diamine (MXD), para-xylylene diamine (PXD ), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, A is a repeating unit XY, (Y) being dodecanedioic acid, (X) corresponds to decanediamine and said diamine (Xi) is chosen from metaxylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD). In an embodiment A is a repeating unit obtained from the polycondensation of a lactam or an amino acid.
    Advantageously, A is C6 to C12 lactam, in particular caprolactam or lauryl lactam.
    Advantageously, A is a C6 to C12 lactam, in particular caprolactam or lauryl lactam and said diamine (X1) is chosen from meta-xylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl ) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, A is lauryl lactam and said diamine (Xi) is chosen from meta-xylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD) .
    Advantageously, A is caprolactam and said diamine (Xi) is chosen from meta-xylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, A is a C6 to C12 amino acid, in particular the aminoundecanoic acid 11.
    Advantageously, A is a C6 to C12 amino acid and said diamine (X1) is chosen from meta-xylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, A is 11-aminoundecanoic acid and said diamine (X1) is chosen from meta-xylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD). In one embodiment, said at least one additive is chosen from fillers, dyes, stabilizers, plasticizers, surfactants, nucleating agents, pigments, brighteners, antioxidants, lubricants, flame retardants, waxes and their mixtures.
    The fillers can be antistatic fillers, silica, graphite, expanded graphite, carbon black, glass beads, kaolin, magnesia, slag, wollastonite, nanofillers (carbon nanotubes) .
    The stabilizers can be organic or mineral stabilizers.
    The plasticizers are, for example, an octyl ester of para-oxybenzoic acid or of Nbutylbenzenesulfonamide.
    Antioxidants are agents against thermo-oxidation and / or photo-oxidation of the polymer of the thermoplastic matrix.
    Nucleating agents such as a metal oxide, metal particles, silica, alumina, clay or talc are known.
    The lubricant can be based on stearate or on a wax binder.
    The flame retardants can be a metal salt chosen from a metal salt of phosphinic acid, a metal salt of diphosphinic acid, a polymer containing at least one metal salt of phosphinic acid, a polymer containing at least one metal salt of diphosphinic acid.
    The waxes can in particular be an amorphous wax, such as a beeswax, a silicone wax, a polyethylene wax, an oxidized polyethylene wax, an ethylene copolymer wax, a montane wax and a wax. polyether.
    According to another aspect, the present invention relates to a composition for use, in particular by injection, comprising:
    - from 25 to 65% by weight, in particular from 35 to 65% of at least one copolyamide
    A / XiY as defined above,
    - from 35 to 75% by weight, in particular from 35 to 65% by weight of glass fibers with circular section,
    - from 0 to 10% by weight of at least one impact modifier,
    - from 0 to 2% by weight of at least one additive, the sum of the proportions of each constituent of the composition being equal to 100%.
    All the characteristics defined for A, X, Y Xi, the glass fibers, the impact modifier and the additive in the context of use are valid for the composition as such.
    Advantageously, said composition for implementation, in particular by injection, comprises:
    - from 25 to 64.9% by weight, in particular from 35 to 64.9% of at least one A / XiY copolyamide as defined above,
    - from 35 to 74.9% by weight, in particular from 35 to 64.9% by weight of glass fibers with circular section,
    - from 0.1 to 10% by weight of at least one impact modifier,
    - from 0 to 2% by weight of at least one additive.
    Advantageously, said composition for implementation, in particular by injection, comprises:
    - from 25 to 64.9% by weight, in particular from 35 to 64.9% of at least one A / XiY copolyamide as defined above,
    - from 35 to 74.9% by weight, in particular from 35 to 64.9% by weight of glass fibers with circular section,
    - from 0 to 10% by weight of at least one impact modifier,
    - 0.1 to 2% by weight of at least one additive.
    Advantageously, said composition for implementation, in particular by injection, comprises:
    - from 25 to 64.8% by weight, in particular from 35 to 64.8% of at least one A / XiY copolyamide as defined above,
    - from 35 to 74.8% by weight, in particular from 35 to 64.8% by weight of glass fibers with circular section,
    - from 0.1 to 10% by weight of at least one impact modifier,
    - 0.1 to 2% by weight of at least one additive.
    Advantageously, the pattern A of the composition for implementation, in particular by injection is a repeating pattern XY.
    Advantageously, the motif A of the composition for implementation, in particular by injection is a repeating motif XY, and (Y) is an aliphatic dicarboxylic acid (Y) at Ü6 to C12, in particular corresponds to the sebacic acid.
    In particular, the motif (X) of the composition for processing, in particular by injection, corresponds to a Ü6 to C12 diamine, in particular hexamethylene diamine or decanediamine.
    Advantageously, the motif (X1) of the composition for implementation, in particular by injection is chosen from meta-xylylene diamine (MXD), paraxylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, the motif A of the composition for implementation, in particular by injection is a repeating motif XY, (Y) being an aliphatic dicarboxylic acid (Y) at C6 to C12 and said diamine (X1) is chosen from meta -xylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, the motif A of the composition for implementation, in particular by injection is a repeating motif XY, (Y) corresponding to sebacic acid and said diamine (X1) is chosen from meta-xylylene diamine (MXD) , para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    In one embodiment, (X) corresponds to a C 6 to C 12 diamine, in particular hexamethylene diamine or decanediamine.
    Advantageously, the motif A of the composition for implementation, in particular by injection is a repeating motif XY, (Y) being an aliphatic dicarboxylic acid (Y) at C6 to C12 and (X) corresponds to a diamine at C6 to C12.
    Advantageously, the motif A of the composition for implementation, in particular by injection is a repeating motif XY, (Y) being an aliphatic dicarboxylic acid (Y) at Ü6 to C12 and (X) corresponds to hexamethylene diamine or decanediamine.
    Advantageously, the motif A of the composition for implementation, in particular by injection is a repeating motif XY, (Y) being an aliphatic dicarboxylic acid (Y) at Ü6 to C12, (X) corresponds to a diamine at Ü6 to C12 and said diamine (X1) is chosen from meta-xylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, the motif A of the composition for implementation, in particular by injection is a repeating motif XY, (Y) being sebacic acid, (X) corresponds to a diamine from C6 to C12 and said diamine (X1) is chosen from meta-xylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, the motif A of the composition for implementation, in particular by injection is a repeating motif XY, (Y) being an aliphatic dicarboxylic acid (Y) at C6 to C12, (X) corresponds to hexamethylene diamine or decanediamine and said diamine (X1) is chosen from meta-xylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, the motif A of the composition for implementation, in particular by injection is a repeating motif XY, (Y) being sebacic acid, (X) corresponds to hexamethylene diamine or decanediamine and said diamine (X1 ) is chosen from meta-xylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, the motif A of the composition for implementation, in particular by injection is a repeating motif obtained from the polycondensation of a lactam or of an amino acid.
    Advantageously, the motif A of the composition for implementation, in particular by injection is a repeating motif obtained from the polycondensation of a C6 to C12 lactam, in particular caprolactam or lauryl lactam.
    Advantageously, the motif A of the composition for implementation, in particular by injection is a repeating motif obtained from the polycondensation of a C6 to C12 lactam, in particular caprolactam or lauryl lactam and said diamine (X1 ) is chosen from meta-xylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, the motif A of the composition for implementation, in particular by injection is a repeating motif obtained from the polycondensation of lauryl lactam and said diamine (Xi) is chosen from meta-xylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, the motif A of the composition for implementation, in particular by injection is a repeating motif obtained from the polycondensation of caprolactam and said diamine (Xi) is chosen from meta-xylylene diamine (MXD), para -xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, A is a C6 to C12 amino acid, in particular the aminoundecanoic acid 11 -.
    Advantageously, the motif A of the composition for implementation, in particular by injection is a repeating motif obtained from the polycondensation of a C6 to C12 amino acid and said diamine (X1) is chosen from meta-xylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    Advantageously, the motif A of the composition for implementation, in particular by injection is a repeating motif obtained from the polycondensation of aminoundecanoic acid and said diamine (X1) is chosen from meta-xylylene diamine (MXD) , para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    In particular, said at least one additive of the composition for use, in particular by injection, is chosen from fillers, dyes, stabilizers, plasticizers, surfactants, nucleating agents, pigments, brighteners, antioxidants, lubricants, flame retardants, waxes and their mixtures.
    According to another aspect, the present invention relates to the use of a composition as defined above to constitute a monolayer structure or at least one layer of a multilayer structure.
    All the characteristics defined above are valid for this use.
    Advantageously, said structure is in the form of an injected part. The injected part can be a telephone part, in particular a phone shell or a part of a computer or tablet or connected watch.
    According to another aspect, the present invention relates to an object obtained from a composition as defined above.
    According to another aspect, the present invention relates to a method for shaping an object as defined above, characterized in that it comprises a step of injecting a composition as defined above.
    According to yet another aspect, the present invention relates to the use of an object as defined above, in the electrical and / or electronic field.
    DESCRIPTION OF THE FIGURES
    Figure 1 (A and B) shows the warping obtained with 2 plates (100 * 100 * 1 mm 3 ) injected by:
    A: composition of the invention (same type of plate for 11 to 18)
    B: composition C1, and measured as described in Example 1.
    A: plate injected with one of compositions 11 to I8 (same type of plate for these different compositions) whose warping is limited and less than 1 mm,
    B: C1 injected plate whose warping is very important and greater than 5 mm.
    EXAMPLES
    Example 1: Evaluation of the warping after 7 days of compositions of (co) polyamides based on CoPA 610 / 1,3BAC10, 610 / 1,4BAC10, 610 / MXD10,
    610 / PXD10, 610 / MPMD10, and circular section glass fibers.
    Synthesis
    The various (comparative) polyamides and copolyamides were prepared according to the usual technique for the synthesis of polyamides and copolyamides.
    Synthesis of CoPa 610 / MXD10 representative of the various copolyamides:
    the hexamethylenediamine, m-xylylenediamine and sebacic acid monomers are loaded together into the reactor according to the desired mass ratio. The medium is first inerted in order to remove the oxygen which can generate yellowing or side reactions. Water can also be charged to improve heat exchange. Two stages of rise in temperature and pressure are achieved. The temperature (T °) and pressure conditions are chosen to allow the medium to be in the molten state. After reaching the holding conditions, degassing takes place to allow the polycondensation reaction. The medium gradually becomes viscous and the reaction water formed is entrained by flushing with nitrogen or placed under vacuum. When the stopping conditions are reached, in connection with the desired viscosity, the stirring is stopped and the extrusion and the granulation can start. The granules obtained will then be compounded with the glass fibers.
    compounding
    The compositions were prepared by melt blending the polymer granules. This mixing was carried out by compounding on an MC26 type twin screw extruder with a flat temperature profile (T °) at 270 ° C. The screw speed is 250rpm.
    The introduction of circular section glass fibers (Nittobo CSX3J451S0) is carried out by side feeding.
    Injection
    Plates of 100 * 100 * 1 mm 3 were prepared by injection of the various compositions:
    - Injection temperature (supply / nozzle): 250/270 ° C
    - Mold temperature: 50 ° C
    The cycle time is adjusted according to the compositions to allow the injection of the compositions. In the case of the injection, it must be less than 50 seconds to be according to the invention.
    Warping was assessed using the method described below:
    The injected plates are placed on a table. The operator presses on 3 angles of the plate to raise the fourth. We then measure the difference between the surface of the table and the sample, see the arrow in Figure 1.
    This measurement is made 7 days after the injection. In the sample on the left in Figure 1 (A), warping is limited, i.e. less than 1mm.
    Inherent viscosity:
    The measurement of the inherent viscosity (I.V.) is carried out in m-cresol. The method is well known to those skilled in the art. We follow the ISO 307: 2007 standard but by changing the solvent (use of m-cresol instead of sulfuric acid; temperature (20 ° C), and concentration (0.5% by mass). It is expressed in dl / g.
    The results are presented in Table I below:
    Comp. CoPA or polyamide (% by weight) Glass fibers with circular section(% in weight) Warping after 7 days Cycle time C1 610I.V.: 0.90 50% > 5 mm <50 s C2 610 / MXD10 (50/50) I.V.: 0.8 50% <1 mm > 50 s C3 MXD10IV: 0.85 50% <1 mm > 50 s 11 610 / MPMD10(80/20)I.V.: 0.91 50% <1 mm <50 s I2 610 / MXD10(80/20)I.V.: 0.98 50% <1 mm <50 s I3 610 / PXD10(70/30)I.V.: 0.95 50% <1 mm <50 s I4 610 / 1,3BAC10 (80/20)I.V.: 0.98 50% <1mm <50 s I5 610 / 1.4BAC10 (80/20)IV: 0.87 50% <1mm <50 s
    Table I
    Comp. means composition.
    Cx stands for comparative composition.
    Ix stands for composition of the invention.
    Example 2: Evaluation of the warping of PA11 compositions of intrinsic viscosity IV = 1.08 or of copolyamide compositions based on PA 11 5 (CoPA 11 / MXD10 (50/50, IV = 0.93), 11 / MXD10 ( 80/20 IV = 0.96), 11 / 1.3BAC10 (80/20, IV = 1.10) and 11 / PXD10 (80/20, IV = 1.15)
    The synthesis, the compounding and the injection are carried out as described for the example with the difference that the mold temperature is 45 ° C and the injection temperature is 260 ° C.
    The results are presented in the following Table II:
    Comp. CoPA or polyamide (% by weight) Glass fibers with circular section (% by weight) Warping after 7 days Cycle time C4 11I.V.: 1.08 50% 3 mm <50 s C5 11 / MXD10(50/50)(IV: 0.93) 50% <1 mm > 50s I6 11 / MXD10(80/20)I.V.: 0.96 50% <1 mm <50 s I7 11 / 1.3BAC10(80/20)IV: 1.10 50% <1 mm <50 s I8 11 / PXD10(80/20)IV: 1.15 50% <1 mm <50 s
    Table II
    权利要求:
    Claims (25)
    [1" id="c-fr-0001]
    claims
    1. Use of a composition comprising at least one semi-crystalline A / XiY copolyamide in which:
    - A is a repeating unit obtained from the polycondensation of at least one lactam at C6 to C12, preferably at C12, or at least one amino acid at C6 to C12, preferably at Cn, or at least a repeating unit XY obtained from the polycondensation of at least one aliphatic diamine (X) at C4 to Cw, in particular at C4 to C12 and at least one aliphatic dicarboxylic acid (Y) at C6 to Cw, in particular in C6 to C12,
    - X1Y is a repeating unit obtained from the polycondensation of a diamine (X1) chosen from an arylamine, a cycloaliphatic diamine and a branched aliphatic diamine, and at least one aliphatic dicarboxylic acid (Y) identical to that of the unit XY, the weight ratio A / X1Y being comprised from 60/40 to 95/5, glass fibers of circular section, and optionally at least one impact modifier and / or at least one additive, to limit warping while keeping the cycle time of the composition obtained adapted to its implementation, in particular by injection.
    [2" id="c-fr-0002]
    2. Use of a composition comprising at least one semi-crystalline A / X1Y copolyamide in which:
    - A is a repeating unit obtained from the polycondensation of a lactam in Ü6 to C12, preferably in C12, or of an amino acid in Ü6 to C12, preferably in C11, or of a repeating unit XY obtained in starting from the polycondensation of an aliphatic diamine (X) at C4 to Cw, in particular at C4 to C12 and an aliphatic dicarboxylic acid (Y) at C6 to Cw, in particular at C6 to C12,
    X1Y is a repeating unit obtained from the polycondensation of a diamine (X1) chosen from an arylamine, a cycloaliphatic diamine and a branched aliphatic diamine, and of an aliphatic dicarboxylic acid (Y) identical to that of the unit XY, the weight ratio A / X1Y being comprised from 60/40 to 95/5, glass fibers with circular section, and optionally at least one impact modifier and / or at least one additive, to limit warping while keeping the time cycle of the composition obtained suitable for its implementation, in particular by injection.
    [3" id="c-fr-0003]
    3. Use according to claim 1 or 2, characterized in that said composition comprises:
    from 25 to 65% by weight, in particular from 35 to 65% of said at least one A / XiY copolyamide,
    - from 35 to 75% by weight, in particular from 35 to 65% by weight of glass fibers with circular section,
    - from 0 to 10% by weight of at least one impact modifier,
    - from 0 to 2% by weight of at least one additive, the sum of the proportions of each constituent of the composition being equal to 100%.
    [4" id="c-fr-0004]
    4. Use according to one of claims 1 to 3, characterized in that said arylamine is chosen from meta-xylylene diamine (MXD) and para-xylylene diamine (PXD).
    [5" id="c-fr-0005]
    5. Use according to one of claims 1 to 3, characterized in that said cycloaliphatic diamine is bis (aminomethyl) cyclohexane (BAC).
    [6" id="c-fr-0006]
    6. Use according to one of claims 1 to 3, characterized in that said branched aliphatic diamine is chosen from 2-methyloctanediamine (MOMD), methylpentamethylene diamine (MPMD) and trimethylhexanemethylenediamine (TM DA).
    [7" id="c-fr-0007]
    7. Use according to one of claims 1 to 6, characterized in that (Xi) is chosen from meta-xylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    [8" id="c-fr-0008]
    8. Use according to one of claims 1 to 7, characterized in that A is a repeating pattern XY.
    [9" id="c-fr-0009]
    9. Use according to claim 8, characterized in that A is a repeating unit XY, and (Y) is an aliphatic dicarboxylic acid (Y) C6 to C12, in particular (Y) corresponds to sebacic acid.
    [10" id="c-fr-0010]
    10. Use according to one of claims 8 or 9, characterized in that (X) corresponds to a C6 to C12 diamine, in particular hexamethylene diamine or decanediamine.
    [11" id="c-fr-0011]
    11. Use according to one of claims 1 to 7, characterized in that A is a repeating unit obtained from the polycondensation of a lactam or an amino acid.
    [12" id="c-fr-0012]
    12. Use according to claim 11, characterized in that A is lactam in Ü6 to C12, in particular lauryl lactam.
    [13" id="c-fr-0013]
    13. Use according to claim 11, characterized in that A is a Ü6 to C12 amino acid, in particular 11-aminoundecanoic acid.
    [14" id="c-fr-0014]
    14. Use according to one of claims 1 to 13, characterized in that said at least one additive is chosen from fillers, dyes, stabilizers, plasticizers, surfactants, nucleating agents, pigments, brighteners , antioxidants, lubricants, flame retardants, waxes and their mixtures.
    [15" id="c-fr-0015]
    15. Composition for implementation, in particular by injection, comprising:
    - from 25 to 65% by weight, in particular from 35 to 65% of at least one copolyamide
    A / X1Y as defined in one of claims 1 to 14,
    - from 35 to 75% by weight, in particular from 35 to 65% by weight of glass fibers with circular section,
    - from 0 to 10% by weight of at least one impact modifier,
    - from 0 to 2% by weight of at least one additive, the sum of the proportions of each constituent of the composition being equal to 100%.
    [16" id="c-fr-0016]
    16. Composition according to claim 15, characterized in that A is a repeating unit XY.
    [17" id="c-fr-0017]
    17. Composition according to claim 16, characterized in that A is a repeating unit XY, and (Y) is an aliphatic dicarboxylic acid (Y) at C 6 to C 12 , in particular corresponds to sebacic acid.
    [18" id="c-fr-0018]
    18. Composition according to one of claims 16 or 17, characterized in that (X) corresponds to a C 2 to C 2 diamine, in particular hexamethylene diamine or decanediamine.
    [19" id="c-fr-0019]
    19. Composition according to one of claims 15 to 18, characterized in that (Xi) is chosen from meta-xylylene diamine (MXD), para-xylylene diamine (PXD), bis (aminomethyl) cyclohexane (BAC) and methylpentamethylene diamine (MPMD).
    [20" id="c-fr-0020]
    20. Composition according to one of claims 15 to 19, characterized in that said at least one additive is chosen from fillers, dyes, stabilizers, plasticizers, surfactants, nucleating agents, pigments, brighteners , antioxidants, lubricants, flame retardants, waxes and their mixtures.
    [21" id="c-fr-0021]
    21. Use of a composition according to one of claims 1 to 14 to constitute a monolayer structure or at least one layer of a multilayer structure.
    [22" id="c-fr-0022]
    22. Use according to claim 21, characterized in that the structure is in the form of an injected part.
    [23" id="c-fr-0023]
    23. Object obtained from a composition as defined in one of claims 1 to 14.
    [24" id="c-fr-0024]
    24. A method of shaping an object according to claim 23, characterized in that it comprises a step of injecting a composition as defined in one of claims 1 to 14.
    [25" id="c-fr-0025]
    25. Use of an object according to claim 23, in the electrical and / or electronic field.
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    同族专利:
    公开号 | 公开日
    FR3071503B1|2020-06-19|
    JP2020535248A|2020-12-03|
    WO2019058077A1|2019-03-28|
    CN111133046A|2020-05-08|
    KR20200058408A|2020-05-27|
    EP3688086A1|2020-08-05|
    US20200262987A1|2020-08-20|
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    US9242892B2|2011-12-06|2016-01-26|Nitto Boseki Co., Ltd.|Glass fibers having non-circular cross sections, and fiber-reinforced resin compact using same|
    CN102675863A|2012-05-11|2012-09-19|金发科技股份有限公司|Low warpage polyamide composite material|
    FR3019181B1|2014-03-31|2020-06-19|Arkema France|POLYAMIDE AND PEBA COMPOSITIONS FOR INJECTING RIGID FATIGUE-RESISTANT PARTS|
    FR3041354B1|2015-09-22|2019-04-19|Arkema France|USE OF A PREPOLYMER IN TRANSPARENT THERMOPLASTIC COMPOSITIONS, COMPOSITIONS COMPRISING THEM AND USES THEREOF|EP3712197A1|2019-03-22|2020-09-23|Arkema France|Use of copolyamides for manufacturing compositions with stable rigidity under the effect of humidity|
    EP3712196A1|2019-03-22|2020-09-23|Arkema France|Use of copolyamides for manufacturing compositions with stable rigidity under the effect of temperature|
    WO2020258266A1|2019-06-28|2020-12-30|Arkema France|Use of a reinforced thermoplastic composition|
    法律状态:
    2019-03-29| PLSC| Search report ready|Effective date: 20190329 |
    2019-08-15| PLFP| Fee payment|Year of fee payment: 3 |
    2020-08-12| PLFP| Fee payment|Year of fee payment: 4 |
    2021-08-12| PLFP| Fee payment|Year of fee payment: 5 |
    优先权:
    申请号 | 申请日 | 专利标题
    FR1758829|2017-09-25|
    FR1758829A|FR3071503B1|2017-09-25|2017-09-25|USE OF A COPOLYAMIDE COMPOSITION AS A MATRIX OF MATERIAL LOADED WITH GLASS FIBERS WITH A CIRCULAR SECTION TO LIMIT YELLOW|FR1758829A| FR3071503B1|2017-09-25|2017-09-25|USE OF A COPOLYAMIDE COMPOSITION AS A MATRIX OF MATERIAL LOADED WITH GLASS FIBERS WITH A CIRCULAR SECTION TO LIMIT YELLOW|
    PCT/FR2018/052327| WO2019058077A1|2017-09-25|2018-09-24|Use of a copolyamide composition as a matrix of filler material with glass fibres having a circular cross section for limiting warping|
    US16/649,737| US20200262987A1|2017-09-25|2018-09-24|Use of a copolyamide composition as a matrix of filler material with glass fibres having a circular cross section for limiting warping|
    EP18783068.2A| EP3688086A1|2017-09-25|2018-09-24|Use of a copolyamide composition as a matrix offiller material with glass fibres having a circular cross section for limiting warping|
    KR1020207008398A| KR20200058408A|2017-09-25|2018-09-24|Use of a copolyamide composition as a matrix of filler material with glass fibers having a circular cross section to limit warping|
    CN201880061594.3A| CN111133046A|2017-09-25|2018-09-24|Use of a copolyamide composition as a matrix of a filler material for glass fibres with a circular cross-section for limiting warping|
    JP2020516449A| JP2020535248A|2017-09-25|2018-09-24|Use of copolyamide composition as a matrix of fillers with glass fibers having a circular cross section to limit warpage|
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