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    • 专利摘要:
    The present invention relates to the use of at least one semicrystalline polyamide in a glass-filled amorphous polyamide resin for the manufacture of a more transparent composition than said resin.
    公开号:FR3018280A1
    申请号:FR1451755
    申请日:2014-03-04
    公开日:2015-09-11
    发明作者:Benjamin Saillard；Maho Yasuda
    申请人:Arkema France SA；
    IPC主号:
    专利说明:

    [0001] The invention relates to the use of novel thermoplastic polymer compositions used for the manufacture of objects having excellent transparency properties, in particular a high transmittance combined with a low Haze. The invention more particularly relates to the manufacture of transparent equipment used in automotive parts, lighting or optical devices, electrical, electronic, and telecommunications, and in particular mobile telephony.
    [0002] By excellent transparency properties within the meaning of the invention are meant materials having: - a transmittance of at least 85% at 560 nm on a 2 mm thick plate (measured according to ISO 13468), - a Haze less than 15% (in Haze unit), measured according to D1003-97. Haze or haze means dullness of surface, haze, sail, "fog", or fog on the surface of the material. This effect is also known as Anglo-Saxon "fogging". This effect can alter the transparency, aesthetics and brightness of the surface of the object. Transparent materials formed from amorphous PA are used for the manufacture of transparent optical devices. They have the advantage of being light, but their rigidity must be improved by the addition of a reinforcing material, such as reinforcing fibers, especially glass fibers, mineral fillers, or rubber components. EP2169008 discloses an amorphous polyamide resin (PA) composition comprising a glass filler, the difference in refractive index between the glass filler and the polyamide not exceeding 0.002. This composition makes it possible to obtain a molded object (2 mm thick plate) having a transmittance of approximately 65% and a Haze of approximately 25%, but these performances prove insufficient to obtain excellent results. transparency as in the case of the present invention. In addition, the high glass transition temperature (Tg), greater than 150 ° C, of these reinforced PA transparent, can make the transformation (including injection) of these materials more difficult, with sometimes problems of removal of material. Today we are looking for more transparent materials (transmittance as high as possible and Haze as low as possible), more rigid, and easy to implement with existing polymer shaping processes or devices. The present invention also aims to provide a method of manufacturing such objects that is simple, easy to implement, fast (which has the least possible steps), and avoids the problems of withdrawal, especially after injection. We have now found a way to obtain an object combining all these properties by the use of at least one semicrystalline polyamide in an amorphous polyamide resin filled with glass.
    [0003] DETAILED DESCRIPTION OF THE INVENTION In the present description, it is specified that: - the terminals are excluded when writing "between" two terminals, and - the terminals are included when writing "the range of X to Z" or "represent X to Y%".
    [0004] The subject of the present invention is therefore the use of at least one semicrystalline polyamide in an amorphous polyamide resin filled with glass for the manufacture of a composition that is more transparent than said resin. The present invention particularly relates to a composition based on polyamide comprising: - semi-crystalline polyamide, - amorphous polyamide, and - a glass filler. Semi-crystalline polyamides within the meaning of the invention are generally understood to mean linear aliphatic polyamides whose crystallinity is manifested by the presence of spherolites of sufficiently large size for the material to have a transmittance of less than 75% at 560 nm 2 mm thick plate (according to ISO 13468.
    [0005] In particular, the semi-crystalline polyamide used in the present invention is chosen from: PA 4.10, PA 4.T, PA 6, PA 6.6, PA 4.6, PA 6.10, PA 6.12, PA 11, PA 12, PA 9.10, PA 9.12, PA 9.13, PA 9.14, PA 9.15, PA 9.16, PA 9.18, PA 9.36, PA 10.10, PA 10.12, PA 10.13, PA 10.14, PA 12.10, PA 12.12, PA 12.13, PA 12.14, PA 6.14, PA 6.13, PA 6.15, PA 6.16, PA 6.18, PA MXD.6, PA MXD.10, PA 12.T, PA 10.T, PA 9.T, PA 18.T, PA 6.T / 6.6, PA 6.6 / 6.T / 61, PA 6 / 6.T. Said semi-crystalline PA represents 5 to 40% by weight, preferably 10 to 30% by weight, preferably 10 to 20% by weight, relative to the total weight of the composition used according to the invention. For the purposes of the invention, the term "amorphous polyamides" means amorphous transparent polyamides (delta Hm (2)) = 0 J / g) or very little semi-crystalline (melting enthalpy at the second DSC heating below 30 J / g), rigid (ISO bending modulus> 1300 MPa), not hot deforming, at 60 ° C, because glass transition temperature Tg greater than 75 ° C. However, they are not very resistant to shock, having a much lower ISO Charpy impact notched compared to the impact modified polyamides, and their chemical resistance is not excellent especially because of their amorphous nature. Transparent amorphous polyamides (homopolyamides or copolyamides) that can be used in the compositions according to the invention are described in particular in patent documents EP1595907 and W009153534. By way of example of transparent amorphous polyamides, mention may be made of PA B.12, PA 11 / B.14 and PA 11 / B.10. Preferably, the transparent amorphous PAs used according to the invention are non-aromatic, so as not to increase the Tg of the composition, to facilitate the homogenization of the composition, not to increase the temperature of transformation or shaping of the composition. composition, and not to risk degrading the other components of the composition. According to the present invention, the amorphous PA comprises more than 50 mol% of an equimolar association of at least one cycloaliphatic diamine and at least one aliphatic dicarboxylic acid, preferably predominantly (to more than 50 mol%) linear, having from 10 to 36, preferably from 10 to 18, carbon atoms.
    [0006] This particular composition of PA (content and chemistry) contributes in particular to obtaining a compliant transparency (transmittance at least equal to 85%, or even at least 90%) to the requirements of the invention. According to a preferred embodiment, the PA used in the invention comprises more than 70%, preferably more than 80%, preferably more than 90%, preferably 100%, in moles, of an equimolar association of at least less a cycloaliphatic diamine and at least one aliphatic dicarboxylic acid, preferably linear, having from 10 to 18 carbon atoms. Said at least one cycloaliphatic diamine is advantageously chosen from: bis (3,5-dialkyl-4-aminocyclohexyl) methane, bis (3,5-dialkyl-4-aminocyclohexyl) ethane, bis (3,5-dialkyl) 4-aminocyclohexyl) propane, bis (3,5-dialkyl-4-aminocyclohexyl) butane, bis (3-methyl-4-aminocyclohexyl) methane (abbreviated "BMACM" or "MACM" or "B "), P-bis (aminocyclohexyl) methane (PACM), isopropylidenedi (cyclohexylamine) (PACP), isophoronediamine (IPD), 2,6-bis (amino methyl) norbornane (BAMN), and their mixtures. Advantageously, a single cycloaliphatic diamine, in particular bis (3-methyl-4-aminocyclohexyl) -methane, is used as a diamine for obtaining PA. At least one non-cycloaliphatic diamine may be present in the composition of the monomers of the PAs, in a proportion of at most 30 mol% (in moles) relative to the diamines of said composition. Non-cycloaliphatic diamines that may be mentioned include linear aliphatic diamines, such as 1,4-tetramethylene diamine, 1,6-hexamethylenediamine, 1,9-nonadiamine and 1,10-decamethylenediamine. The C10-C18 aliphatic dicarboxylic acid is preferably selected from 1,10-decanedicarboxylic acid or sebacic acid, 1,12-dodecanedicarboxylic acid, 1,14-tetradecanedicarboxylic acid and 1,18-tetradecanedicarboxylic acid. - octadecanedicarboxylic. The dicarboxylic acid may optionally be at least partially branched by at least one C 1 to C 3 alkyl group (having 1 to 3 carbon atoms). At least one non-aliphatic dicarboxylic acid can be used in the composition of the monomers of AP in a proportion of at most 15 mol% relative to the dicarboxylic acids of the PAs. Preferably, the non-aliphatic dicarboxylic acid is chosen from aromatic diacids, in particular isophthalic acid (I), terephthalic acid (T) and mixtures thereof. The term "monomer" in the present description of polyamides should be understood as "repetitive unit". Indeed, the case where a repeating unit of the PA consists of the combination of a diacid with a diamine is particular. It is considered that it is the combination of a diamine and a diacid, that is to say the diamine.diacide couple (in equimolar quantity), which corresponds to the monomer. This is explained by the fact that, individually, the diacid or the diamine is only a structural unit, which is not enough on its own to polymerize. Said PA may optionally comprise less than 50 mol% of at least one polyamide comonomer, that is to say a monomer of different composition from said equimolar majority association defined above. Preferably, said PA comprises less than 30 mol%, preferably less than 20%, preferably less than 10% of polyamide comonomer (s), said at least one comonomer may be selected from lactams, alpha-omega acids aminocarboxylic, diamine associations. diacid different from that defined above, and mixtures thereof. The lactam is, for example, selected from caprolactam, oenantholactam and lauryllactam. The alpha-omega-aminocarboxylic acid is, for example, selected from aminocaproic acid, 7-amino-heptanoic acid, 11-amino-undecanoic acid or 12-amino-dodecanoic acid. Preferably, PAs are formed essentially (at more than 80 mol%) from at least one monomer selected from B.10, B.12, B.14, B.16, B.18, their copolymers (copolyamides). ) and / or blocks, and their mixtures. Said amorphous PA represents 20 to 80% by weight, preferably 30 to 70% by weight, preferably 40 to 70% by weight, relative to the total weight of the composition used according to the invention. Examples of amorphous polyamide resin types include: polyamide PA12 / MACMI (PA12 / 3,3-dimethyl-4,4-diaminocyclohexylmethane, isophthalic acid), PA12 / MACMT (PA12 / 3,3-dimethyl) -4,4-diaminocyclohexylmethane, terephthalic acid), PA MACM 12 (3,3-dimethyl-4,4-diaminocyclohexylmethane, decanedicarboxylic acid or laurolactam), PA MC 12 (PA12, 1,3-bis) (aminomethyl) cyclohexane), PA6I / 6T, and PA6I / 6T / MACMI. Commercially available PAs such as Grilamid TR55® containing PA12 / MACMI, Grilamid TR90e containing PAMACM12, manufactured by EMSChemie, and Trogamid CX® manufactured by Evonik Degussa-Chemie) containing PA MC 12, and Rilsan can be used. ® Clear containing PA12 / MACMT (manufactured by ARKEMA). By glass filler within the meaning of the invention is meant a filler comprising (or even consisting of), expressed in% by weight, 68 to 74% of silicon dioxide (SiO 2), 2 to 5% of aluminum oxide ( A1203), 2 to 5% boron oxide (B2O3), 2 to 10% calcium oxide (CaO), 0 to 5% zinc oxide (ZnO), 0 to 5% of strontium oxide (SrO), 0 to 1% barium oxide (BaO), 1 to 5% magnesium oxide (MgO), 0 to 5% lithium oxide (Li2O), 5 to 12% of sodium oxide (Na2O), and 0 to 10% of potassium oxide (K2O), in which the total amount of lithium oxide (Li2O), sodium oxide (Na2O), and potassium oxide (K2O) is 8 to 12%. In the polyamide composition of the present invention, it is preferable that the difference in refractive index between the glass filler and the resin component is: 0.002 or less with respect to light having a wavelength of 589 nm ; 0.002 or less with respect to light having a wavelength of 486 nm, and 0.002 or less with respect to light having a wavelength of 656 nm. Preferably, the amorphous polyamide resin composition of the present invention uses a glass filler having, in its composition, a total content of calcium oxide (CaO) and magnesium oxide (MgO) of 3 to 15% by weight on the total weight of the composition. Preferably, the amorphous polyamide resin composition of the present invention uses a glass filler having, in its composition, a total content of silicon dioxide (SiO 2) and aluminum oxide (Al 2 O 3) of 70 to 79% by weight on the weight of the composition.
    [0007] Preferably, the amorphous polyamide composition of the present invention utilizes a glass filler which is, in its composition, substantially or completely free of titanium oxide (TiO 2).
    [0008] Preferably, the amorphous polyamide composition of the present invention has a glass filler content of 5 to 40% by weight, based on the weight of the composition. Advantageously, the glass filler used in the composition according to the invention comprises at least one element chosen from: a glass fiber, a glass powder, glass flakes, a crushed fiber, and a glass ball. The present invention also relates to a molded article manufactured by molding the composition according to the invention. The very small difference between the refractive indices of the amorphous polyamide resin and the glass filler, even after the reinforcement with the glass filler, makes it possible to obtain a molded product having a very high transparency. In the amorphous polyamide resin composition of the present invention, the difference in refractive index between the composition containing the amorphous polyamide resin and the glass filler is preferably 0.002 or less with respect to a light having a length of wave of 589 nm, 0.002 or less with respect to light having a wavelength of 486 nm, and 0.002 or less with respect to light having a wavelength of 656 nm. Each of these differences is even more preferably 0.001 or less with respect to the aforementioned three wavelengths of light. If each of the refractive index differences between the resin component containing the amorphous polyamide resin and the glass filler is greater than 0.002 with respect to three aforementioned wavelengths of light, a molded product produced by molding the Polyamide resin composition will not be transparent. The refractive index of the composition containing the amorphous polyamide resin is preferably from 1.505 to 1.545 with respect to light having a wavelength of 589 nm; 1.512 to 1.555 with respect to light having a wavelength of 486 nm and 1.502 to 1.541 with respect to light having a wavelength of 656 nm. In particular, in order to reduce the differences between the refractive indices between the resin component and the glass filler, the refractive indices of the resin component containing the amorphous polyamide resin are particularly preferably: from 1.508 to 1.520 by to a light having a wavelength of 589 nm; 1.515 to 1.527 with respect to light having a wavelength of 486 nm, and from 1.505 to 1.517 with respect to light having a wavelength of 656 nm. The glass filler used in the polyamide composition of the present invention comprises or consists of, expressed in terms of oxides in% by weight, on the weight of the composition: 68 to 74% of silicon dioxide (SiO 2), 2 to 5% of aluminum oxide (Al 2 O 3), 2 to 5% of boron oxide (B2O 3), 2 to 10% of calcium oxide (CaO), 0 to 5% of zinc oxide (ZnO), from 0 to 5% of strontium oxide (SrO), from 0 to 1% of barium oxide (BaO), 1 to 5% of magnesium oxide (MgO), from 0 to 5% lithium oxide (Li2O), 5 to 12% sodium oxide (Na2O), and 0 to 10% potassium oxide (K2O), where a total amount of lithium oxide (Li2O), sodium oxide (Na2O), and potassium oxide (K2O) is 8 to 12%. The glass filler preferably contains silicon dioxide (SiO2) in a concentration of 68 to 74%, and preferably 68 to 72%. If the content of silicon dioxide (SiO2) is less than 68%, it is difficult to match the refractive index of the glass filler with that of the amorphous polyamide resin. On the other hand, if the content of silicon dioxide (SiO 2) exceeds 74%, the solubility of the glass filler in the composition is greatly reduced. In particular, in the case where the glass filler is used in the form of fiberglass, the spinning temperature is high, which leads to production difficulties. The glass filler preferably contains aluminum oxide (Al 2 O 3) in a concentration of 2 to 5%, and preferably 2 to 4%. If the aluminum oxide content (Al 2 O 3) is less than 2%, the chemical resistance to water is reduced.
    [0009] On the other hand, if the aluminum oxide content (Al 2 O 3) is greater than 5%, the glass tends to be heterogeneous. The total content of silicon dioxide (SiO 2) and aluminum oxide (Al 2 O 3) is preferably 70 to 79%, and more preferably 71 to 76%. It is then easy to compare the refractive index of the glass load with the refractive index of the amorphous polyamide resin. Advantageously, the glass filler contains sodium oxide (Na2O) in a content of 5 to 12%, and preferably 8 to 11%. If the content of sodium oxide (Na2O) content exceeds 12%, the water resistance of the glass tends to decrease. On the other hand, if the sodium oxide content content (Na 2 O) is less than 5%, it is difficult to compare the refractive index of the glass filler with the refractive index of the amorphous polyamide resin.
    [0010] The glass filler may contain lithium oxide (Li 2 O) in a concentration of 0 to 5%, and preferably 0 to 2%. The glass filler may contain potassium oxide (K2O) in a concentration of 0 to 10%, and preferably 0 to 5%. Sodium oxide (Na2O) may be partially substituted with lithium oxide (Li2O) or potassium oxide (K2O), which improves the water resistance of the glass. The glass filler may contain alkaline components, lithium oxide (Li2O), sodium oxide (Na2O), and potassium oxide (K2O), in a concentration of 8 to 12%, and preferably from 8 to 11% in total. If the total amount of the alkaline components is greater than 12%, the water resistance of the glass tends to decrease. On the other hand, if the total amount of the alkaline components is less than 8%, it is difficult to produce the glass filler because the glass becomes difficult to melt. Preferably, the glass filler contains calcium oxide (CaO) in a concentration of 2 to 10%, and preferably 6 to 9%. If the calcium oxide (CaO) content is less than 2%, the melting ability of the glass tends to decrease. On the other hand, if the content of calcium oxide (CaO) exceeds 10%, it is difficult to compare the refractive index of the glass filler with the refractive index of the amorphous polyamide resin. Zinc oxide (ZnO) is an optional component, and the glass filler may contain zinc oxide in a concentration of 0 to 5%, preferably 0 to 2%. The addition of zinc oxide (ZnO) can improve the water resistance of the glass. However, it is preferred that zinc oxide (ZnO) content not exceed this upper limit because glass tends to be devitrified. Strontium oxide (SrO) is an optional component, and the glass filler may contain strontium oxide in a concentration of 0 to 5%, and preferably 0 to 2%.
    [0011] Barium oxide (BaO) is an optional component, and the glass filler may contain barium oxide in a concentration of 0 to 1%. The total content of calcium oxide (CaO), zinc oxide (ZnO), strontium oxide (SrO) and barium oxide (BaO) is preferably 4 to 10%, and more preferably 6 to 10%. If the total content of these elements is less than 4%, the melting ability of the glass is lower. On the other hand, if their content exceeds 10%, it is difficult to compare the refractive index of the glass filler with the refractive index of the amorphous polyamide resin. The glass filler preferably contains magnesium oxide (MgO) at a concentration of 1 to 5%, and preferably 1 to 3%. The addition of magnesium oxide (MgO) can improve the mechanical properties of the glass. A magnesium oxide (MgO) content exceeding 5% is not recommended because the melting ability of the glass tends to decrease. The glass filler preferably contains boron oxide (B2O3) in a concentration of 2 to 5%, and preferably 2 to 4%. A content of boron oxide (B2O3) with a content of less than 2% is undesirable because it becomes difficult to bring the refractive index of the glass filler closer to the refractive index of the amorphous polyamide resin. A content of boron oxide (B2O3) exceeding 5% is not preferred because of the formation of volatile compounds during melting of the glass, which can lead to corrosion problems in the production facilities or require additional equipment for the collection of volatile compounds. The TiO 2 content of the glass filler is preferably less than 0.1%. Ideally, the glass filler is free of titanium oxide (TiO2) to prevent staining phenomena.
    [0012] The glass filler or composition of the present invention may contain one or more components other than the aforementioned components, such as, for example, an oxide of a metal such as Fe, Co, Ni, Sn, Zr, Mo. The previously described glass filler used according to the present invention has a refractive index of 1.505 to 1.545 with respect to a light having a wavelength of 589 nm, a refractive index of 1.512 to 1.555 with respect to a light having a wavelength of 486 nm, and a refractive index of 1.502 to 1.541 with respect to a light having a wavelength of 656 nm, and these refractive indices are substantially the same as those of the resins of amorphous polyamides. Therefore, the glass filler can be used for the production of a molded product amorphous polyamide resin having high transparency and excellent mechanical strength.
    [0013] For example, if the glass filler contains 68 to 72% silicon dioxide (SiO2), 2 to 4% aluminum oxide (Al2O3), 2 to 4% boron oxide (B2O3), 6 to 9% calcium oxide (CaO), 0 to 2% zinc oxide (ZnO), 0 to 2% strontium oxide (SrO), 0 to 1% barium oxide (BaO ), from 1 to 3% of magnesium oxide (MgO), from 0 to 2% of lithium oxide (Li2O), from 8 to 11% of sodium oxide (Na2O), and from 0 to 5% of oxide of potassium (K2O), the glass filler tends to have a refractive index of 1.508 to 1.520 with respect to a light having a wavelength of 589 nm, a refractive index of 1.515 to 1.527 with respect to a light having a wavelength of 486 nm, and a refractive index of 1.505 to 1.517 with respect to light having a wavelength of 656 nm.
    [0014] Silicon dioxide (SiO2), aluminum oxide (Al2O3), and alkaline components can decrease the refractive index of the glass filler. Examples of components which can decrease the refractive index of the glass filler other than the above-mentioned components include P2O5 and F2. Therefore, in the case where the refractive index of the glass filler is smaller than the desired refractive index, namely the refractive index of the amorphous polyamide resin, the refractive index can be increased for example, by substituting with calcium oxide (CaO) a portion of the silicon dioxide (SiO2). For example, if 0.4% calcium oxide (CaO) is substituted for 0.4% silicon dioxide (SiO2), the refractive index of the glass filler increases by about 0.002. In the case where the refractive index of the glass filler is higher than the desired refractive index, namely the refractive index of the amorphous polyamide resin, the refractive index can be lowered, for example by substituting with an alkaline compound part of the calcium oxide (CaO). Specifically, for example, if 0.8% sodium oxide (Na2O) is substituted for 0.5% calcium oxide (CaO), the refractive index of the glass charge decrease decreases by approximately 0.002.
    [0015] The refractive index of the glass filler can be suitably adjusted, and it is possible to produce a glass filler having the same range of refractive index as the refractive index of the amorphous polyamide resin. In the present invention, the glass filler used may comprise (or even consist of): glass fiber, glass powder, glass flakes, milled fiber, or glass bead. Of these possible forms of glass filler, fiberglass is preferred for its strength. It is similar to a conventional reinforcing fiber such as fiberglass E, and has a high efficiency in reinforcing the amorphous polyamide resin molded product. Fiberglass can be produced by any conventional spinning process for continuous fiberglass. For example, it is possible to fibrillate the glass by various processes such as the direct melting process, in which the glass is subjected to vitrification continuously in an oven and then introduced into a crucible, and subjected to spinning by a mounted socket at the bottom of the crucible, and the reflow process in which molten glass is transformed into a ball or rod, followed by re-melting and spinning. The diameter of the glass fiber is preferably 5 to 50 μm, preferably 10 to 45 μm. Glass powder can be produced by any production process, such as glass melting followed by water granulation. The particle size is preferably 1 to 100 μm. The glass filler may also be in the form of flakes or flakes of glass, which may be produced by any conventional production processes, such as by spraying the melt. The thickness of the glass flakes is preferably from 0.1 to 10 μm. Crushed fibers can be produced by any known conventional method. For example, ground fiber can be produced by spraying a strand of a glass fiber using a hammer mill or ball mill. The diameter of the fiber and the length to diameter ratio of the ground fiber are preferably 5 to 50 μm and 2 to 150, respectively.
    [0016] Glass beads may be produced by any conventionally known production method, for example, by melting and spraying the glass melt. The particle size of the glass beads is preferably from 5 to 300 μm.
    [0017] In the present invention, two or more charge forms selected from: glass fiber, glass powder, glass flakes, milled fiber, and glass beads may be used in combination as a glass filler. Advantageously, the glass filler is surface-treated with a coupling agent to increase the affinity and adhesion between the resin component containing the amorphous polyamide resin and the glass fiber, which avoids any reduction in the transparency of the glass. molded product caused by the formation of voids. As coupling agent, mention may be made of those based on silane, borane, aluminates, those of titanate type, and the like. In particular, silane coupling agents are preferred because they allow good adhesion between the amorphous polyamide resin and the glass filler. As the silane coupling agent, aminosilane coupling agents, epoxysilanes, acrylsilane, and the like can be used. Of the silane coupling agents, aminosilane coupling agents are preferred. In addition, the charge treatment may optionally include film forming agents, lubricating agents, antistatic agents and the like, in addition to the coupling agent. These components can be used alone or in combination. Examples of film-forming agents that may be mentioned are vinyl acetate, urethane, acrylic, polyester, polyether, phenoxy, polyamide, epoxy resins, and / or the like. Examples of lubricating agents that may be mentioned are the aliphatic ester, the aliphatic ether, the aromatic ester or surfactants containing aromatic ethers. As an example of an antistatic agent, mention may be made of inorganic salts such as lithium chloride or potassium iodide, as well as quaternary ammonium salts such as ammonium chloride or ammonium ethosulphate.
    [0018] In the present invention, the filler content of glass in the polyamide composition is preferably from 5 to 40% by weight, preferably from 5 to 20% by weight, relative to the total weight of the composition. If the filler content of glass is less than 5% by weight, the molded product obtained by molding the polyamide resin composition tends to have poor mechanical properties, whereas if the filler content of glass is greater than 40 % by weight, the contact area between the resin and the glass filler is increased, which tends to reduce the moldability and transparency of the molded product obtained. When the amount of the glass filler in the polyamide composition is in the range mentioned above, it is possible to produce a molded product combining both good mechanical properties and excellent transparency. The composition according to the invention may further comprise at least one block copolymer (s) PE and block (s) PA, hereinafter PEBA comprising one or more PE blocks and one or more PA blocks. The abbreviated "PEBA" polyether block and polyamide block copolymers result from the polycondensation of reactive end polyamide blocks with reactive end polyether blocks, such as, inter alia: 1) polyamide blocks with diamine chain ends with polyoxyalkylene blocks with dicarboxylic chain ends. 2) polyamide blocks with dicarboxylic chain ends with polyoxyalkylene blocks with diamine chain ends, obtained by cyanoethylation and hydrogenation of aliphatic alpha-omega dihydroxylated polyoxyalkylene blocks called polyetherdiols; 3) polyamide blocks with dicarboxylic chain ends with polyetherdiols, the products obtained in this particular case are polyetheresteramides. The polyamide blocks with dicarboxylic chain ends come, for example, from the condensation of polyamide precursors in the presence of a chain-limiting dicarboxylic acid. The polyamide blocks with diamine chain ends come for example from the condensation of polyamide precursors in the presence of a chain-limiting diamine. The molar mass in number Mn of the polyamide blocks is between 400 and 20000 g / mol and preferably between 500 and 10000 g / mol. Polymers with polyamide blocks and polyether blocks may also comprise randomly distributed units.
    [0019] Three types of polyamide blocks can advantageously be used. According to a first type, the polyamide blocks come from the condensation of a dicarboxylic acid, in particular those having from 4 to 20 carbon atoms, preferably those having from 6 to 18 carbon atoms and an aliphatic or aromatic diamine, in particular those having 2 to 20 carbon atoms, preferably those having 6 to 14 carbon atoms. Examples of dicarboxylic acids that may be mentioned include 1,4-cyclohexyldicarboxylic acid, butanedioic, adipic, azelaic, suberic, sebacic, dodecanedicarboxylic, octadecanedicarboxylic acids and terephthalic and isophthalic acids, but also dimerized fatty acids. . Examples of diamines that may be mentioned include tetramethylene diamine, hexamethylenediamine, 1,10-decamethylenediamine, dodecamethylenediamine, trimethylhexamethylenediamine, isomers of bis (4-aminocyclohexyl) methane (BACM), (3-methyl-4-aminocyclohexyl) methane (BMACM), and 2-2-bis- (3-methyl-4-aminocyclohexyl) propane (BMACP), and para-amino-di-cyclohexyl methane (PACM). ), and isophoronediamine (IPDA), 2,6-bis (aminomethyl) -norbornane (BAMN) and piperazine (Pip). Advantageously, PA4.12, PA4.14, PA4.18, PA6.10, PA6.12, PA6.14, PA6.18, PA9.12, PA10.10, PA10.12, and PA10.14 blocks are used. PA10.18.
    [0020] According to a second type, the polyamide blocks result from the condensation of one or more alpha omega-aminocarboxylic acids and / or one or more lactams having from 6 to 12 carbon atoms in the presence of a dicarboxylic acid having from 4 to 12 carbon atoms or a diamine. Examples of lactams include caprolactam, oenantholactam and lauryllactam. As examples of alpha omega amino carboxylic acid, mention may be made of aminocaproic acid, amino-7-heptanoic acid, amino-11-undecanoic acid and amino-12-dodecanoic acid. Advantageously, the polyamide blocks of the second type are made of polyamide 11, polyamide 12 or polyamide 6.
    [0021] According to a third type, the polyamide blocks result from the condensation of at least one alpha omega aminocarboxylic acid (or a lactam), at least one diamine and at least one dicarboxylic acid.
    [0022] In this case, the polyamide PA blocks are prepared by polycondensation of: - the linear or aromatic aliphatic diamine or diamines having X carbon atoms; - Dicarboxylic acid (s) having Y carbon atoms; and - comonomer (s) {Z} chosen from lactams and alpha-omega aminocarboxylic acids having Z carbon atoms and equimolar mixtures of at least one diamine having X 1 carbon atoms and at least one dicarboxylic acid having Y 1 carbon atoms, (X 1, Y 1) being different from (X, Y), said comonomer (s) being introduced in a proportion by weight of up to 50%, preferably up to 20%, still more preferably up to 10% with respect to all of the polyamide precursor monomers; in the presence of a chain limiter chosen from the dicarboxylic acids Advantageously, the dicarboxylic acid having Y carbon atoms is used as chain limiter, which is introduced in excess relative to the stoichiometry of the diamine or diamines. According to a variant of this third type, the polyamide blocks result from the condensation of at least two alpha omega aminocarboxylic acids or at least two lactams containing from 6 to 12 carbon atoms or a lactam and an aminocarboxylic acid. not having the same number of carbon atoms in the possible presence of a chain limiter. By way of example of aliphatic alpha omega amino carboxylic acid, mention may be made of aminocaproic, amino-7-heptanoic, amino-11-undecanoic and amino-12-dodecanoic acids. By way of example of lactam, there may be mentioned caprolactam, oenantholactam and lauryllactam. As examples of aliphatic diamines, there may be mentioned hexamethylenediamine, dodecamethylenediamine and trimethylhexamethylenediamine. As an example of cycloaliphatic diacids, mention may be made of 1,4-cyclohexyldicarboxylic acid. Examples of aliphatic diacids that may be mentioned include butane dioic acid, adipic acid, azelaic acid, suberic acid, sebacic acid, dodecanedicarboxylic acid and dimerized fatty acids (these dimerized fatty acids preferably have a dimer content of at least 98%). they are preferably hydrogenated and are sold under the trade name "PRIPOL" by the company "UNICHEMA", or under the trademark EMPOL by the company HENKEL) and the polyoxyalkylenes - a, co diacids. As examples of aromatic diacids, mention may be made of terephthalic (T) and isophthalic (I) acids. By way of example of cycloaliphatic diamines, mention may be made of the isomers of bis- (4-aminocyclohexyl) methane (BACM), bis (3-methyl-4-aminocyclohexyl) methane (BMACM), and 2-2-bis - (3-methyl-4-aminocyclohexyl) propane (BMACP), and para-amino-di-cyclohexylmethane (PACM). Other diamines commonly used may be isophoronediamine (IPDA), 2,6-bis (aminomethyl) -norbornane (BAMN) and piperazine.
    [0023] By way of examples of polyamide blocks of the third type, mention may be made of the following: 6.6 / 6 in which 6.6 denotes hexamethylenediamine units condensed with adipic acid. 6 denotes patterns resulting from the condensation of caprolactam. - 6.6 / 6.10 / 11/12 wherein 6.6 denotes hexamethylenediamine condensed with adipic acid. 6.10 denotes hexamethylenediamine condensed with sebacic acid. 11 denotes units resulting from the condensation of aminoundecanoic acid. 12 denotes patterns resulting from the condensation of lauryllactam.
    [0024] Said PE blocks represent 10 to 80% by weight, preferably 20 to 60% by weight, preferably 20 to 40% by weight, relative to the total weight of the copolymer. The number-average molecular mass of the PE blocks is between 200 and 1000 g / mol (excluding bounds), preferably in the range of 400 to 800 g / mol (inclusive), preferably 500 to 700 g / mol.
    [0025] The PE blocks (polyether) are for example derived from at least one polyalkylene ether polyol, in particular a polyalkylene ether diol, preferably chosen from polyethylene glycol (PEG), polypropylene glycol (PPG), polytrimethylene glycol (PO 3 G), polytetramethylene glycol (PTMG) and mixtures or copolymers thereof. The PE blocks may comprise polyoxyalkylene sequences with NH 2 chain ends, such sequences being obtainable by cyanoacetylation of aliphatic polyoxyalkylene alpha-omega dihydroxylated sequences known as polyetherdiols. More particularly, it is possible to use Jeffamines (for example Jeffamine® D400, D2000, ED 2003, XTJ 542, commercial products from Huntsman). Said at least one PE block preferably comprises at least one polyether chosen from polyalkylene ether polyols, such as PEG, PPG, PO3G, PTMG, polyethers containing polyoxyalkylene sequences with NH2 chain ends, and their copolymers (copolyethers). ) and / or blocks, and their mixtures. The subject of the present invention is in particular a composition containing: from 5 to 40% by weight of semi-crystalline polyamide as defined above, from 20 to 80% by weight, by weight of at least one transparent amorphous polyamide at least partially cycloaliphatic, preferably non-aromatic, - from 5 to 40%, preferably from 5 to 30%, by weight of glass filler - from 0 to 5% of PEBA - from 0 to 5% of additives, the total weight of the composition, and its use for the manufacture of an object of transparency in accordance with that defined above according to the invention. The chemical composition of said amorphous polyamide is preferably chosen from the compositions already described for the polyamide blocks of the PEBAs above, which ensures compatibility of the PA with the PEBA. The addition of such a content of block copolymer to the composition according to the invention makes it possible to improve the processability of the composition: improved fluidity (or flow capacity) and ductility while retaining its transparency properties. The injection of the composition according to the invention is easy, and causes very little removal of material after injection, which allows to obtain parts of high dimensional accuracy. Said semi-crystalline PA, amorphous PA, and any PEBA used in the composition of the invention preferably have substantially the same refractive index measured according to ISO 489 as. It is also possible to play on the nature of the raw materials used to synthesize PEBA and PA. In general, the addition of an aromatic compound (for example an aromatic diacid) increases the refractive index of a product. For PEBA, the refractive index decreases if, for example, the PTMG content is increased, relative to the pure PA of the same composition as the PA block of PEBA. In the BMACM.Y series of PAs, Y being an aliphatic diacid, the longer Y is, the lower the refractive index. For a linear aliphatic PA, the more the number of CH2 increases in the pattern, the lower the refractive index. If there is an additive other than a glass filler or a PEBA in the composition, this additive is present from 0.01 to 5% by weight relative to the total weight of the composition. The additive is chosen in particular from coloring agents, in particular pigments, dyes, effect pigments, such as diffractive pigments, interferential pigments, such as pearlescent agents, reflecting pigments and their mixtures; anti-UV agents, anti-aging agents, antioxidants, fluidizing agents, anti-abrasion agents, release agents, stabilizers, plasticizers, impact modifiers, surfactants, brighteners, fillers, fibers, waxes and mixtures thereof, and / or any other additive well known in the field of polymers. Among the non-glass fillers previously described, there may be mentioned silica, carbon black, carbon nanotubes or expanded graphite.
    [0026] The use according to the invention makes it possible to obtain a more transparent object which is easier to use than an object of the same shape made of amorphous polyamide loaded with glass, as shown in the tables of the examples below. According to an advantageous embodiment, the composition of the invention is manufactured by compounding or by dry blending ("dry blend") of its various components. Dry blending is preferred because it comprises fewer steps and generally entails less risk of pollution (blackheads, gels) of the composition than by compounding. Said composition can be used according to the invention to manufacture granules or powders, which can be in turn used in conventional polymer shaping processes for the manufacture of filaments, tubes, films, plates and / or or transparent molded objects.
    [0027] The present invention particularly relates to a method of manufacturing a transparent object, said method comprising: - a semi-crystalline polymer supply step according to that defined above; a step of mixing said copolymer with at least one transparent amorphous PA and at least one glass filler and / or at least one PEBA and / or at least one additive, so as to manufacture a composition as defined above; a stage of implementation, in particular in a mold or a die, of the copolymer or of the composition at a temperature T 0 in the range from 50 to 120 ° C, preferably from 60 to 100 ° C, preferably from 60 to 100 ° C; at 95 ° C; - then a step of recovery of the transparent object. By "implementation" is meant here any method of shaping polymers, such as molding, injection, extrusion, coextrusion, hot pressing, multi-injection, rotational molding, sintering, laser sintering, etc., from the composition according to the invention. For the process for manufacturing objects, in particular molded, injected or extruded according to the invention, the granules are preferred. Powdered with a volume median diameter (measured according to ISO 9276 - Parts 1 to 6) in the range of 400 to 600 μm is used more rarely. According to a particular mode of shaping of the process of the invention, in particular by sintering such as "laser sintering" or by rotomoulding, the compositions according to the invention are preferably in the form of powder whose particles have a diameter median volume less than 400 i_tm, preferably less than 200 i_tm. Powder manufacturing methods include cryogenic milling and microganulation. Another possible embodiment of the process of the present invention may further comprise a preliminary step of compounding PA with dyes, and / or any other additive, prior to said step of making granules or powder.
    [0028] The invention also relates to the use of a composition as defined above for the manufacture of a transparent equipment, such as glasses, frames and / or glasses, a ballistic glass, a transparent plate, a helmet, visor, shield, scuba; sports equipment; a watch glass; space equipment, including satellite, space shuttle; aeronautical or automotive equipment, such as a windshield, a window, a porthole, a cockpit, an airplane canopy, a window, a window, in particular a car or a construction window, a window of a projector, Lighthouse ; a display window, in particular advertising, electronic, computer; a screen element; a panel of thermal, solar, photovoltaic panel; an article in the building, furnishing, appliance and decoration industry; play, toy; fashion, such as shoe heels, jewelry; furniture, such as a table, seat, armchair; an article or presentation element; packaging, case, case; container, flask, perfume article, cosmetic or pharmaceutical industry; a bag ; a protection element during transport; a protective shell of computer, electronic or telecommunication equipment, especially telephone. The present invention also relates to any transparent object of composition in accordance with that defined above.
    [0029] Examples The examples below illustrate the present invention without limiting its scope. In the examples, unless otherwise indicated, all percentages and parts are by weight. Transparent amorphous polyamides used: PAamI: PA 11 / B.10 comprising less than 80 mol% of a monomer B.10 (in which "10" represents sebacic acid with 10 carbon atoms) and more than 20 mol% of a comonomer formed by amino-11-undecanoic acid. PAam2: PA 11 / B.10 comprising more than 80 mol% of a monomer B.10 (in which "10" represents sebacic acid with 10 carbon atoms) and less than 20 mol% of a comonomer formed by 11-amino-undecanoic acid.
    [0030] These polyamides are prepared according to the method described in patent document WO2009153534, page 12, line 21 to page 9. - Glass fibers used: those corresponding to EP2169008 and marketed by Asahi Fiber Glass Company - Semi-crystalline polyamide used PAsc: PA 11 with a viscosity of less than 1.3 (inherent viscosity measured according to the ARKEMA method: 0.5 g / dL in metacresol at 25 ° C.) PEBA used: PA 12-PTMG (with a number of molecular masses of PA blocks) - PE: 2000 - 1000).
    [0031] All the aforementioned PA and PEBA are marketed by Arkema. Transparency properties: transmittance and Haze are measured on a 2 mm thick plate. The transparency properties are tested on standard specimens according to the standards used and indicated in Table 1. The flow properties (MVR), such as the flow length, of the compositions are also measured in Table 3. under the same test conditions "Spiral flow test" (speed of rotation of the screw, the supply temperature of the nozzle at the injection point, etc.). These plates and test pieces are obtained by injection from granules of PAam, PAsc, glass fillers, and any PEBA and additives, previously dry mixed, of compositions specified above, and as indicated in Tables 2 and 3. Table 1 shows that only Examples 1 to 4 (Exl to Ex4) according to the invention combine high transparency (transmittance greater than 75% and Haze less than 15%, at 560 nm on a 2 mm thick plate, measured at using a Konica-Minolta 3610d spectrophotometer, according to ISO 13468) and better fluidity (MVR greater than 10), unlike comparisons 1 to 3 (Cpl-Cp3). Table 1 Haze (ASTM D1003-97) Transmittance (560 nm, 2mm, ISO 13468) Table 2 Ex 3 Cp 3 I Ex 4 15.7 7.7 18.8 1 Tm: 70 ° C, PAamI-GF 15% - MB1% 1 Tm: 70 ° C, PAAMI - GF 15% - PAsc 10% -MB 1% thickness (mm) Haze (D1003-97) (C) Transmittance (560 nm) Test no. 18 85 Cpl 2 19 83 EXR 2 8 85 3 13 81 Tm, Composition MVR (275 ° C., 2.16 kg) 10.2 Test No. PAsc 10 PAlaml PAam 2 PEBA GF Blue MB Total (%) Tg (° C) DSC (° C / min) Table 3 Cp 2 Ex 2 0 20 84 54 5 5 10 20 1 1 100 100 127 102 10 0 30 64 64 34 5 5 20 30 100 100 100 123 142 118 Transmittance Injection temperature: 60 ° C. 80 ° C 95 ° C 81 86 87 84 87 84 88 Haze Injection temperature: 60 ° C 80 ° C 95 ° C 45.6 18.4 9.9 30.1 8.4 30.3 5.1 20 25
    权利要求:
    Claims (23)
    [0001]
    CLAIMS1- Use of at least one semicrystalline polyamide in an amorphous polyamide resin filled with glass for the manufacture of a polyamide composition more transparent than said resin.
    [0002]
    2- Use according to claim 1, wherein the semicrystalline polyamide is chosen from: PA 4.10, PA 4.T, PA 6, PA 6.6, PA 4.6, PA 6.10, PA 6.12, PA 11, PA 12, PA 9.10, PA 9.12, PA 9.13, PA 9.14, PA 9.15, PA 9.16, PA 9.18, PA 9.36, PA 10.10, PA 10.12, PA 10.13, PA 10.14, PA 12.10, PA 12.12, PA 12.13, PA 12.14, PA 6.14, PA 6.13, PA 6.15, PA 6.16, PA 6.18, PA MXD.6, PA MXD.10, PA 12.T, PA 10.T, PA 9.T, PA 18.T, PA 6.T / 6.6 , PA 6.6 / 6.T / 6.I, PA 6 / 6.T, and mixtures thereof.
    [0003]
    A transparent polyamide-based composition made according to the use of any one of claims 1 or 2, comprising: - from 5 to 40% by weight of semi-crystalline polyamide, - from 20 to 80% by weight, at least one at least partially cycloaliphatic transparent amorphous polyamide, 5 to 40%, preferably 5 to 30%, by weight of glass filler, and optionally: 0 to 5% by weight of PEBA; 5% by weight of additives, on the total weight of the composition.
    [0004]
    4. Composition according to claim 3, in which the glass filler comprises, expressed in terms of oxides in% by weight on the total weight of filler, 68 to 74% of silicon dioxide (SiO2) of 2 to 5%. aluminum oxide (Al 2 O 3), 2 to 5% boron oxide (B2O 3), 2 to 10% calcium oxide (CaO), 0 to 5% zinc oxide (ZnO) ), from 0 to 5% of strontium oxide (SrO), from 0 to 1% of barium oxide (BaO), from 1 to 5% of magnesium oxide (MgO), from 0 to 5% d lithium oxide (Li2O), from 5 to 12% of sodium oxide (Na2O) and from 0 to 10% of potassium oxide (K2O), in which the total amount of lithium oxide (Li2O), sodium oxide (Na2O) and potassium oxide (1 (20) varies from 8 to 12%.
    [0005]
    5. Composition according to claim 3 or 4, characterized in that the differences between the refractive indices of the glass filler and the polyamide resin are: 0.002 or less for a wavelength of 589 nm; 0.002 or less for light of wavelength 486 nm; and 0.002 or less for a light having a wavelength of 656 nm; and the polyamide composition has a transmittance of 85% or more and a Haze less than 15% when the composition is molded into a 2 mm thick plate.
    [0006]
    6. Composition according to any one of claims 3 to 5, characterized in that the glass filler has a total content of silicon dioxide (SiO2) and aluminum oxide (A1203) of 71 to 76% expressed in terms of oxides in% by weight.
    [0007]
    7- Composition according to any one of claims 3 to 6, characterized in that the glass filler has a content of silicon dioxide (SiO2) of 68 to 72 ° A.
    [0008]
    8- Composition according to any one of claims 3 to 7, characterized in that the glass filler has an Na2O content of 8 to 11%.
    [0009]
    9- Composition according to any one of claims 3 to 8, characterized in that the glass filler has an Al 2 O 3 content of 2 to 4%.
    [0010]
    10-. Composition according to any one of Claims 3 to 9, characterized in that the glass filler has a CaO content of 6 to 9%.
    [0011]
    11- Composition according to any one of claims 3 to 10, characterized in that the glass filler has a MgO content of 1 to 3%.
    [0012]
    12- Composition according to any one of claims 3 to 11, characterized in that the glass filler has a B203 content of 2 to 4%.
    [0013]
    13. Composition according to any one of claims 3 to 12, characterized in that the glass filler has a total content of calcium oxide (CaO), zinc oxide (znO), strontium oxide (SrO) and in barium oxide (BaO) of 4 to 10%.
    [0014]
    14. Composition according to any one of Claims 3 to 13, characterized in that the glass filler has a total content of lithium oxide (Li 2 O), sodium oxide (Na 2 O) and potassium oxide (K 2 O). from 8 to 11%.
    [0015]
    15. Composition according to any one of claims 3 to 14, characterized in that the glass filler is free of titanium oxide (TiO 2).
    [0016]
    16. Composition according to any one of claims 3 to 15, characterized in that the amorphous polyamide resin composition has a glass filler content of 5 to 40% by weight. 20
    [0017]
    17- Composition according to any one of claims 3 to 16, characterized in that the glass filler comprises at least one component selected from the group consisting of glass fibers, glass powder, glass flakes, crushed fibers , glass beads, and mixtures thereof. 25
    [0018]
    18- Composition according to any one of claims 3 to 17, characterized in that it further comprises at least one additive selected from: dyes, including pigments, dyes, effect pigments, such as pigments diffractants, interferential pigments, such as nacres, reflective pigments and mixtures thereof; anti-UV agents, anti-aging agents, antioxidants; fluidizing agents, anti-abrasion agents, release agents, stabilizers; plasticizers, modifierschocs; surfactants; brighteners; fillers, such as silica, carbon black, carbon nanotubes, expanded graphite; fibers; waxes; and their mixtures.
    [0019]
    19- Use of a composition as defined in one of claims 3 to 18 to form granules or powders.
    [0020]
    Use of granules as defined in claim 19 for producing filaments, tubes, films, plates and / or transparent moldings.
    [0021]
    21- Molded product based on polyamide, characterized in that it is manufactured by molding, injection, extrusion, coextrusion, hot pressing, multi-injection, rotomoulding, sintering and / or laser sintering, a polyamide composition according to Any of claims 3 to 18.
    [0022]
    22. A method of manufacturing a transparent object reinforced glass fillers, said method comprising: a semi-crystalline polymer supply step; A step of mixing said semi-crystalline polyamide with at least one transparent amorphous PA and at least one glass filler and optionally at least one PEBA and / or at least one additive, so as to produce a composition according to any one of the claims 3 to 18 a step of implementation, in particular in a mold or a die, of the composition at a temperature TO in the range from 50 to 120 ° C, preferably from 60 to 100 ° C, preferably from 60 to 100 ° C. at 95 ° C; - then a step of recovery of the transparent object. 30
    [0023]
    23- Use of a composition according to any one of claims 3 to 18 for the manufacture of a transparent equipment, such as glasses, frames and / or glasses, a ballistic glass, a transparent plate, a mask, a visor , a shield, a diving suit; sports equipment; a watch glass; space equipment, including satellite, space shuttle; aeronautical or automotive equipment, such as a windshield, a window, a porthole, a cockpit, an airplane canopy, a window, a window, in particular a car or a construction window, a window of a projector, Lighthouse ; a display window, in particular advertising, electronic, computer; a screen element; a panel of thermal, solar, photovoltaic panel; an article in the building, furnishing, appliance and decoration industry; play, toy; fashion, such as shoe heels, jewelry; furniture, such as a table, seat, armchair; an article or presentation element; packaging, case, case; container, flask, perfume article, cosmetic or pharmaceutical industry; a bag ; a protection element during transport; a protective cover for a computer, electronic or telecommunication device, particularly a telephone.
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    同族专利:
    公开号 | 公开日
    CN106255725B|2019-09-13|
    US10246587B2|2019-04-02|
    JP6515114B2|2019-05-15|
    WO2015132510A1|2015-09-11|
    KR20160129889A|2016-11-09|
    TW201602236A|2016-01-16|
    JP2017510677A|2017-04-13|
    FR3018280B1|2017-05-26|
    KR20180069101A|2018-06-22|
    TWI663212B|2019-06-21|
    KR102320618B1|2021-11-01|
    EP3114171A1|2017-01-11|
    US20160369098A1|2016-12-22|
    CN106255725A|2016-12-21|
    CN110483983A|2019-11-22|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US4404317A|1981-07-09|1983-09-13|E. I. Du Pont De Nemours & Co.|Polyamide blends|
    EP0628602A1|1993-06-11|1994-12-14|Elf Atochem S.A.|Transparent polyamide compositions without heat deformation|
    EP1227131A1|2001-01-26|2002-07-31|Atofina|Transparent polyamide containing composition|
    EP1595907A1|2004-05-14|2005-11-16|Arkema|Transparent amorphous polyamides based on diamines and on tetradecanedioic acid|
    EP1942147A1|2006-12-28|2008-07-09|Ems-Chemie Ag|Polyamide moulding materials reinforced with flat glass fibers and articles injection-moulded therefrom|
    WO2009153531A1|2008-06-20|2009-12-23|Arkema France|Polyamide, composition comprising such a polyamide, and uses thereof|
    US20100076155A1|2008-09-25|2010-03-25|Asahi Fiber Glass Company|Amorphous polyamide resin composition and molded product|
    EP2169008A1|2008-09-25|2010-03-31|Asahi Fiber Glass Company, Limited|Amorphous polyamide resin composition and molded product|
    US20100160008A1|2008-12-23|2010-06-24|E. I. Du Pont De Nemours And Company|Low sink marks and excellent surface appearance reinforced polyamide compositions|
    US20100249292A1|2009-03-30|2010-09-30|E. I. Du Pont De Nemours And Company|Flame resistant semicaromatic polyamide resin composition and articles therefrom|
    US20130022786A1|2011-07-21|2013-01-24|E I Du Pont De Nemours And Company|Device housings having excellent surface appearance|
    JPS6228983B2|1981-07-09|1987-06-23|Ii Ai Deyuhon De Nimoasu Ando Co|
    JP4174355B2|2003-03-10|2008-10-29|住友ベークライト株式会社|Transparent composite composition|
    FR2871808B1|2004-06-22|2006-10-13|Arkema Sa|USE OF A MICRO-CRYSTALLINE POLYAMIDE TO OBTAIN A PARTICULAR SURFACE CONDITION|
    US7833450B2|2004-06-22|2010-11-16|Arkema France|Use of a microcrystalline polyamide to obtain a particular surface finish|
    US7799713B2|2005-11-04|2010-09-21|Ocv Intellectual Capital, Llc|Composition for high performance glass, high performance glass fibers and articles therefrom|
    WO2008047672A1|2006-10-16|2008-04-24|Idemitsu Kosan Co., Ltd.|Flame-retardant polycarbonate resin composition, polycarbonate resin molded article, and method for producing the polycarbonate resin molded article|
    JP5140315B2|2007-05-14|2013-02-06|旭ファイバーグラス株式会社|Amorphous polyamide resin composition and molded article|
    FR2932808B1|2008-06-20|2010-08-13|Arkema France|COPOLYAMIDE, COMPOSITION COMPRISING SUCH COPOLYAMIDE AND USES THEREOF|
    CN101684195B|2008-09-25|2013-03-27|旭玻璃纤维股份有限公司|Non-crystalline polyamide resin composition and product thereof|
    EP2706092B1|2012-08-28|2014-12-24|Ems-Patent Ag|Polyamide moulding material and its application|
    EP2746342B1|2012-12-21|2015-10-21|Ems-Patent Ag|Stain-resistant articles and their use|
    WO2015090435A1|2013-12-20|2015-06-25|Ems-Patent Ag|Long-fibre-reinforced polyamides|US10544286B2|2015-02-13|2020-01-28|Ems-Patent Ag|Polyamide moulding composition and moulded article made from this moulding composition|
    FR3043681B1|2015-11-17|2020-01-10|Arkema France|AMORPHOUS POLYAMIDE COMPOSITION HAVING IMPROVED DIMENSIONAL STABILITY|
    EP3184577A1|2015-12-23|2017-06-28|Ems-Patent Ag|Method and container for storing and transporting polyamide pellets and correspondingly stored or transported polyamide pellets and shaped articles obtained therefrom|
    EP3455056B1|2016-05-13|2021-09-22|Hewlett-Packard Development Company, L.P.|Material sets|
    FR3051475B1|2016-05-17|2020-02-21|Arkema France|TRANSPARENT SHOCK RESISTANT COMPOSITION|
    CN106118003B|2016-07-29|2018-06-22|佛山市高明区诚睿基科技有限公司|A kind of modified reinforced polyester glass-reinforced plastic material and preparation method thereof|
    CN106243658B|2016-07-29|2018-08-28|佛山市高明区诚睿基科技有限公司|A kind of high-performance polyester glass-reinforced plastic material of durable antibiotic and preparation method thereof|
    CN106189151B|2016-07-29|2018-06-01|佛山市高明区诚睿基科技有限公司|A kind of composite glass fiber reinforced polyester glass-reinforced plastic material and preparation method thereof|
    EP3309199B1|2016-10-12|2020-04-01|Ems-Patent Ag|Glass filler reinforced polyamide molding materials based on amorphous copolyamides|
    EP3312224B1|2016-10-21|2018-12-26|Ems-Patent Ag|Polyamide moulding composition and multi-layered structure made herefrom|
    EP3444112B1|2017-08-18|2020-12-23|Ems-Chemie Ag|Reinforced polyamide moulding compounds with low haze and moulds therefrom|
    EP3444113B1|2017-08-18|2021-01-20|Ems-Chemie Ag|Reinforced polyamide moulding compounds with low haze and moulds therefrom|
    EP3444114A1|2017-08-18|2019-02-20|EMS-Patent AG|Reinforced polyamide moulding compounds with low haze and moulds therefrom|
    EP3450481B1|2017-08-31|2020-10-21|Ems-Chemie Ag|Polyamide moulding material having high gloss and high notch impact strength|
    EP3461854A1|2017-09-27|2019-04-03|Arkema France|Transparent polyamide-based composition comprising a glass filler with low silica content|
    EP3691900A1|2017-10-04|2020-08-12|Basf Se|Sintered powder containing a near-infrared reflector for producing moulded bodies|
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    EP3502164A1|2017-12-22|2019-06-26|EMS-Patent AG|Polyamide moulding material|
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    FR3087444B1|2018-10-17|2020-10-02|Arkema France|TRANSPARENT POLYMERIC COMPOSITION|
    KR102240966B1|2018-12-28|2021-04-15|롯데첨단소재|Polyamide resin composition and article comprising the same|
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    WO2020227847A1|2019-05-10|2020-11-19|Evonik Operations Gmbh|Polyamide composition|
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    法律状态:
    2016-02-08| PLFP| Fee payment|Year of fee payment: 3 |
    2017-02-13| PLFP| Fee payment|Year of fee payment: 4 |
    2018-02-23| PLFP| Fee payment|Year of fee payment: 5 |
    2020-02-14| PLFP| Fee payment|Year of fee payment: 7 |
    2021-02-10| PLFP| Fee payment|Year of fee payment: 8 |
    2022-02-09| PLFP| Fee payment|Year of fee payment: 9 |
    优先权:
    申请号 | 申请日 | 专利标题
    FR1451755A|FR3018280B1|2014-03-04|2014-03-04|TRANSPARENT COMPOSITION BASED ON POLYAMIDE CHARGED WITH GLASS|FR1451755A| FR3018280B1|2014-03-04|2014-03-04|TRANSPARENT COMPOSITION BASED ON POLYAMIDE CHARGED WITH GLASS|
    EP15711254.1A| EP3114171A1|2014-03-04|2015-02-27|Transparent composition based on glass-charged polyamide|
    JP2016555506A| JP6515114B2|2014-03-04|2015-02-27|Transparent polyamide composition comprising glass as filler|
    KR1020187016588A| KR102320618B1|2014-03-04|2015-02-27|Transparent composition based on glass-charged polyamide|
    PCT/FR2015/050475| WO2015132510A1|2014-03-04|2015-02-27|Transparent composition based on glass-charged polyamide|
    CN201580023198.8A| CN106255725B|2014-03-04|2015-02-27|The transparent composition of polyamide based on glass-filled|
    CN201910763029.8A| CN110483983A|2014-03-04|2015-02-27|The transparent composition of polyamide based on glass-filled|
    KR1020167027487A| KR20160129889A|2014-03-04|2015-02-27|Transparent composition based on glass-charged polyamide|
    US15/123,420| US10246587B2|2014-03-04|2015-02-27|Transparent polyamide-based composition comprising glass as filler|
    TW104106684A| TWI663212B|2014-03-04|2015-03-03|Transparent polyamide-based composition comprising glass as filler|
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